How did this spider evolve to mimic exactly a human face and arms?

How did this spider evolve to mimic exactly a human face and arms?

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So I came across something terribly amazing today, that is, a video showing this species of peacock-spider, that literally, transforms into a human face waving his arms about.

What could have possibly given rise to this?

I can understand the arms waving around, but why the uncanny human-face template, complete with eyes, nose, mouth, etc.

I do not believe this to be a case of anthropomorphism on my part, (seeing what I am familiar with), because I cannot imagine any other natural case where such symmetry in a pattern would closely resemble a human face.

Would appreciate any explanation. Thanks!

I think this really is just a case of what you refer to in your question as anthropomorphism. We are very, very good at seeing faces. Here are some more examples.


This site has pictures of quite a few peacock spiders, and as far as I can tell these are all the same species (The only peacock spider mentioned on Wikipedia is Maratus volans).

The remarkable thing about these images is that individual spiders seem to have very different patterns on thorax and abdomen, and many of these are much less like human faces. This seems to me to weaken the case for some sort of mimicry.

Interesting fact: seeing faces and other forms where they do not exist is a psychological phenomenon called pareidolia.

Peacock spiders certainly aren't mimicking human faces, and I strongly doubt they're mimicking anything at all. As others have noted, it's the combination of a fluke, and some anthropomorphising on your part (easy to do!).

The stunning colours and 'dancing' are actually part of a courtship display, and are most likely under strong sexual selection, rather than selection for any anti-predator function. The male-limited colours are only on display during courtship, and are otherwise flattened along the abdomen. It's also worth remembering that these spiders are tiny (< 5 mm), so the only other animals that are likely to be able to resolve those patterns in any detail are similarly sized organisms with decent eyesight (i.e. female peacock spiders).

Madeline Girard is in the latter-stages of her PhD on these guys, I'd recommend shooting her an e-mail if you're really interested.

In part, the way the spider resembles a human face is due to bilateral symmetry in the body shape and coloring of the spider. Bilateral symmetry evolved early in the animal kingdom to facilitate streamlining of the body (which makes it move faster in any fluid, including air and water), formation of a central nervous system and a head. Human faces (and bodies) are also bilaterally symmetric, hence the resemblance.

Another reason, as you note, is antropomorphism - the ability of humans to see a human face in many natural shapes and colorings. Other animals, including predators probably also have this ability to see faces in nature. This allowed the spider to evolve to imitate a scary face. This is called mimicry and it helps the spider ward off predators.

There are 44 species of peacock spider known to date and each species has a unique pattern on the thorax. Although this patterns can often resemble human faces, the likelihood of this being is the case is almost impossible because that would mean that humans would have to be present right at the beginning and throughout the evolution of these species.

They are endemic to Australia and as you may know Australia has vast areas of Australia that have only been inhabited humans for short periods. The process of evolution take much longer than a few generations. This similarity should be seen as more of a beautiful coincidence than any sort of mimicry

source - MSc dissertation written on the fascinating little creatures

Humanoid vs Bipedaloid Word Diction

I'm doing an extensive write-up project, and I'm stumped for how an alien species similar to the human analogue morphology (Two Arms, Two Legs, and Plantigrade-Bipedal standing/maneuvering) should be called. I don't want to go for Humanoid, because that's to on the nose and too humancentric for the type of setting I'm developing.

I want something more neutral, so I went for the terminology "Bipedaloid", but I don't know how easily parse-able a person seeing that at face value would know I'm denoting to a rough morphology similar too a human.

Do you think such a terminology I thought up is good or feasible, or can there be a suggestion for anything else that can help?

Mimicry, Camouflage and Perceptual Exploitation: the Evolution of Deception in Nature

Despite decades of study, mimicry continues to inspire and challenge evolutionary biologists. This essay aims to assess recent conceptual frameworks for the study of mimicry and to examine the links between mimicry and related phenomena. Mimicry is defined here as similarity in appearance and/or behavior between a mimic and a model that provides a selective advantage to the mimic because it affects the behavior of a receiver causing it to misidentify the mimic, and that evolved (or is maintained by selection) because of those effects. Mimics copy cues or signals that are already in use as part of a stable communication system, but offer misleading information to receivers. Mimicry overlaps, both conceptually and evolutionarily, with camouflage and perceptual exploitation but the overlap is only partial, which may create some confusion. Certain types of camouflage (e.g. masquerade) conform to the definition of mimicry, while others (e.g. background matching) are not considered mimicry because they prevent detection rather than recognition of the camouflaged animal. Mimicry, on the other hand, works by exploiting peculiarities of the receiver at higher stages of sensory processing involving recognition and classification of stimuli. Perceptual exploitation models of trait evolution are also closely related to mimicry, and sensory traps in particular may act as a precursor for true mimicry to evolve. The common thread through these diverse phenomena is deception of a receiver by a mimic. Thus receiver deception (i.e. perceptual error) emerges as a key characteristic of mimicry shared with some types of camouflage and perceptual exploitation.

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15 Examples of the Most Epic Metamorphoses from Youth to Adult

We’re all familiar with the most dramatic metamorphosizers of the animal kingdom: butterflies. They go from a tiny egg to an awkward wiggling caterpillar to mysterious pupa to a delicate, colorful winged creature. However, there are many other animals besides butterflies that undergo dramatic transformations from youth to adult. Here are 15 of the most epic metamorphoses seen in nature.


What’s black, white, and red all over? Many ladybugs are—but only in their final stage of life. Turns out these little beetles undergo one of the most epic metamorphoses in the animal kingdom: For most species, after adult female ladybugs mate, they lay a clutch of tiny yellow eggs right in the middle of an aphid colony, usually on the underside of a leaf. Eggs hatch in a week, revealing spiky black worm-like larvae that readily gobble up the aphids around them. When a larva is fully grown, it changes into a blob-like yellow pupa. Finally, the black, white and red (or sometimes yellow or orange) insect appears.


Mayflies, the less-elegant cousins of dragonflies and damselflies, have one of the most unique metamorphoses of all insects. Most insects’ life stages move from egg to nymph to pupa to adult, but mayflies do not have a pupa stage. Instead, it is the only type of insect to undergo a subimago stage, meaning it’s almost an adult in the sense it grows wings … but cannot fly long distances and isn’t yet sexually mature. The mayfly’s final life stage, the fully flighted and sexually mature imago or adult, is extremely short, lasting just a few hours to a few days.


are tiny, venomous, and beautiful (especially the colorfully rumped males) arthopods native to Australia. Male peacock spiders are so beautiful, in fact, it’s hard to believe that, like all spiders, they go through some not-so-glamorous life stages: egg, egg sac, spiderling, adult. When male peacock spiders reach sexual maturity they try to seduce less-colorful female peacock spiders by performing a showy dance.


While adult nudibranchs are essentially colorful and ornate blobs of the sea, they don’t start out that way. In fact, after hatching, nudibranch larvae are tiny, plain-looking and have small snail-like shells. Over the course of two months they morph from this plain stage into adults, along the way getting larger and more colorful, losing their shells, and growing gills and feelers, called rhinophores.


Another sea creature that looks completely different as an adult than a juvenile is the crown of thorns starfish. When looking at an adult, it’s easy to see where this creature gets its name: It’s completely covered with dangerous-looking sharp spikes. But after hatching, it looks like not much more than a translucent, floating blob. Over time it grows arms, and later, spikes, then fixes itself to rocks where it feeds on coral.


The secret to a long and prosperous life, it turns out, is to be a jellyfish. The aptly named immortal jellyfish begins life as an egg, like all other jellies. It then enters the free-swimming larva stage, then settles down into a polyp on the ocean floor, and then finally morphs into a sexually mature jellyfish. Unlike most other jellies, an immortal jellyfish is capable of reverting back into the polyp stage at any time it faces environmental stress, attacks by predators, sickness or old age—essentially being reborn as a young jelly.


Think of Pablo Picasso’s most asymmetrically painted human face, stick it onto a fish, and there you have a flatfish. These fish, which include flounder and sole among other species, begin life inside tiny eggs that float up to the surface of the sea. For a few weeks, a larval flatfish swims upright and looks just like a typical baby fish. But after a few weeks its skull bones shift and one eye migrates to the opposite side of its face, forcing the now-lopsided fish to swim sideways. Eventually, when its facial features all move to one side of its face, it changes color and moves to live on the bottom of the sea, its blind side facing down.


Also called the snot otter and devil dog, the eastern hellbender is a giant type of salamander not exactly known for being beautiful in its adult form. Slippery, wrinkly and the color of mud, they’re right at home at the bottom of rivers, where they can live up to 50 years. Like all salamanders, hellbenders begin as eggs. From their eggs they hatch, coming into the world small and adorable. As time passes, they grow larger and less cute.


Don’t let this lime-green frog’s bright and cheery looks fool you: It lives in only one tiny area in India and is critically endangered, threatened most by an ever-shrinking habitat. These creatures were once believed to lay eggs that developed into tadpoles on pond surfaces like many other frogs. But in 2014, it was discovered that they had a different reproductive strategy: The frogs crawl into a living bamboo shoot that has a hole in it (probably created by insects or rodents) and lay their eggs there. The creatures skip the tadpole stage entirely, hatching as froglets. Because they don't have a tadpole stage, the species doesn't require water to lay its eggs.


Covered in bright hues spotted, striped, banded, and blotched with contrasting black, the poison dart frog is one of the most striking-looking of all amphibians. Yet they don’t start out that way. After hatching, young mimic poison dart frogs are looked after by their mother, who lays a clutch of unfertilized feeder eggs to provide them with some nourishment (and, at least for some species of poison dart frog, toxicity). Tadpoles are brown and black, growing more colorful with age until they reach their fantastic adult form.


The kea is a large, vulnerable species of parrot native to New Zealand, with green and blue feathers on its back and brown and orange feathers on its underside. While adult keas appear majestic and beautiful, they don’t start out that way. Baby keas retain an alien-like, sparse white hairdo for several months after hatching. Keas are considered a very intelligent species, observed working together and using tools.


Laysan albatrosses are another species of bird where the babies are very little like their parents. But unlike baby keas, baby Laysan albatrosses hatch as adorable fuzzy gray blobs. As they grow older, the babies slowly grow adult feathers and lose their baby feathers. This leaves them with unique hairdos that sometimes make them look like human celebrities. Ringo Starr, anyone?


Unlike keas and albatrosses, baby flamingoes look a lot like their parents, except they’re missing something: color. Flamingo chicks hatch with gray and/or white feathers, over time taking on the same pink hue as their parents, which becomes more intense over time. Why? Well, you are what you eat, and flamingoes eat shrimp and algae rich in carotenoids, the same pigments that cause shrimp to turn pink when cooked.


Virginia opossums are scavengers, eating carrion and rotting vegetation, and that helps keep the environment clean. Virginia opossums are native to North America, where they’re the continent’s only living marsupials. These opossums have pouches for carrying their babies, just like kangaroos. Also like kangaroos they give birth to large numbers of navy-bean-size babies, which grow inside their pouches. When they’re born, they look more like pink jellybeans than animals. Over the course of three to five months, they mature, growing fur, sharp teeth and long tails.


Giant pandas are called giant pandas for a reason: They’re enormous in size, weighing up to 250 pounds. But these bamboo-munching bears don’t start out that way. When born, giant panda cubs weigh just 90 to 130 grams (about as much as a small apple). Besides being way smaller in size, baby pandas are also quite sparsely furred—and so they look very different than what they will as fuzzy black-and-white adults.

What Might Life on Other Planets Look Like? A Harvard Biologist Explains

Jonathan B. Losos is a biology professor and director of the Losos Laboratory at Harvard University and Curator of Herpetology at Harvard&rsquos Museum of Comparative Zoology. His research regularly appears in top scientific journals, such as Nature and Science, and he has written a popular series about his work for The New York Times. Losos is the editor in chief of The Princeton Guide to Evolution and a member of the National Geographic Society&rsquos Committee for Research and Exploration. He is the author of Lizards in an Evolutionary Tree: Ecology and Adaptive Radiation of Anoles.

Jonathan B. Losos: So this question about the inevitability of evolution, the extent to which the outcomes we see in the world today were destined to occur, has a number of implications.

I mean just most generally it tells us whether how fated evolution was to occur, how the outcome today was destined in a way.

But it has other implications as well that people have long speculated about, and that is: what would life be like on other planets if it is evolved? Would it be like the world today here on Earth or would it be completely different?

And this question has taken on some increased urgency or at least interest in recent years because we now realize that there are many planets out there that are like Earth. We used to think that Earth was perhaps unique and so perhaps life as we know it is unique, because we&rsquore the only place that it could evolve.

But quite the contrary we&rsquove now discovered that there are lots of what are called &ldquohabitable exoplanets&rdquo, Some people estimate millions, even billions just in our own Milky Way galaxy. So if that&rsquos the case, if there are that many Earth-like planets &ndash and by Earth-like I mean about the same size, temperature, atmosphere somewhat similar, running water &ndash roughly similar conditions. If there are really that many Earth-like planets many people think that it&rsquos very likely that life has evolved on them.

And so the question is what will that life look like? Well there are those who argue that from the argument of convergent evolution they argue that species facing the same conditions here on Earth evolved the same solutions by natural selection.

They extrapolate to say if conditions on other planets are similar to here then we would see very similar lifeforms, that you arrive on whatever planet you&rsquoll see animal and plant-like organisms that look very familiar. Some people have gone so far as to say that, in fact, human type organisms, humanoids will occur on other planets. So there will be intelligent beings that if we saw them they would be recognizable which, of course, is what Hollywood tells us. If you watch almost any science fiction TV show or movie the intelligent lifeform is bipedal, a couple of arms, a mouth. Maybe they only have three fingers and pointy ears and they&rsquore green, but they&rsquore pretty humanoid.

And so some people say yes, that&rsquos actually very likely that humans are a very successful lifeform here on Earth that we are extremely well adapted to our environment which ancestrally was occurring on the plains of Africa. But we have adapted so exquisitely that we now dominate the world. And so if this is such a good adaptation here on Earth it would similarly be a good adaptation on another planet and evolution would be likely to take the similar course. That is the argument that is being made in some quarters.

Not everyone is convinced by this argument that evolution is deterministic. We recognize that convergent evolution does occur more than we used to realize but still it is argued and I agree with this viewpoint, it&rsquos not inevitable. And the reason is that there are often multiple ways to adapt to the same environmental circumstance. And so even though species are faced with the same conditions they may find different ways to adapt to them. And my favorite example of that has to do with a bird that everyone knows &ndash the woodpecker. And everyone&rsquos heard the tat-tat-tat of a woodpecker on a tree or on your garage siding or whatever. People don&rsquot actually know what the woodpecker is doing.

This is what the woodpecker is doing: It is using its beak to pound on dead wood, listening for a hollow space, the echo indicating there&rsquos a hollow space in the wood which is where a grub, a larval beetle or some other insect is eating the dead wood. And so it listens for the sound of a hollow space. When it hears it, it then starts tapping very hard &ndash tat-tat-tat-tat-tat-tat &ndash using its beak as a jackhammer to dig into the, to chisel or to dig into the deep wood to get to the tunnel. Once it&rsquos there&mdashthe woodpecker has an extremely long tongue. So long, in fact, that it wraps around its brain case. But it sticks out this long tongue that has little prickles on it, and the tongue goes in and it snags the grub which looks like a mealworm or a &ndash snags the grub and pulls it out and eats it. And that is how they capture the food that they eat.

Well woodpeckers are found on almost every continent in the world. They&rsquore very successful, but they don&rsquot fly very well across water. They don&rsquot like to fly across water. And so isolated islands tend not to have woodpeckers. And in their absence other species have evolved to fill the same niche.

And the most extreme example of a different way of doing the same thing is an animal on the island of Madagascar called an aye-aye. Now an aye-aye is a type of lemur. Now people know lemurs from the TV show Zooboomafoo and maybe they&rsquove seen them, the ring-tailed lemur. They hop around, very cute, and so on.

The aye-aye is not very cute. It&rsquos about the size maybe of a small housecat and it&rsquos kind of demonic looking. It has these big leathery ears and these bright yellow eyes and a face that only a mother can love. And the native people of Madagascar had all kinds of taboos and myths about them because they look &ndash and they only come out at night. But their most extreme feature that I think really kind of freaks people out is that their third finger is long and extremely thin. It looks skeletal, and it can rotate in any direction. It&rsquos this kind of finger that can wiggle around.

Anyway, they live the same lifestyle as a woodpecker. They&rsquore looking for the same grubs in dead wood. But they do it in a completely different way. Instead of tapping with their peak they tap with their finger. They go around the wood going tap-tap-tap and their big ears are rotated forward listening for the sound of an echo.

And when they hear the echo of an empty tunnel they have these teeth that are &ndash these teeth are kind of sticking out like this, these chiseling incisors that are very strong. And they bite their way through the wood and bite into the wood until they get the tunnel. And then once they get there they then use their finger again. They stick it in there and they snag the larvae and pull it out. And so they&rsquore doing exactly the same thing that the woodpecker is doing but they&rsquove evolved a completely different set of adaptations. And so that&rsquos just one example of how species can adapt to do the same thing in very different ways.

And we see many examples of that in the world. Conversely we also see many examples of species that have no evolutionary parallel. What we call an evolutionary singleton. That is a species that is very well adapted to where it lives but no other species has done the same thing. And my favorite example of that is the duck-billed platypus, this extraordinary animal in Australia. Now people like to make fun of the platypus but they don&rsquot realize that the platypus is exquisitely adapted to living in the streams in eastern Australia. And so it has very lush fur that allows it to swim in water that&rsquos basically almost at freezing It has a powerful tail It&rsquos got webbed feet for swimming And then most extraordinarily it has this duck bill. Now it&rsquos not actually &ndash it kind of looks like a duck&rsquos bill, but it&rsquos not hard like a duck&rsquos bill.It&rsquos actually leathery.

But more importantly it&rsquos covered with thousands of little receptors and these receptors there&rsquos two types of them. One of them can detect slight variation in ripples of water. And so if something goes swimming by they can detect it in the water But in addition they have electro receptors. They can detect very slight electrical discharges. And so when an animal moves its muscles there&rsquos a little bit of electrical activity, and the platypus can detect that. And so when it&rsquos swimming under water it closes its eyes, its ears and its mouth, but based on the receptors on its bill it can find its way around and it can locate its prey&mdashRemarkable adaptation to eating crayfish and other food items like that.

Well so, the platypus lives in these streams that are in no way remarkable. There are streams like that behind the house I grew up in in St. Louis and they occur around the world. Yet nowhere else has a duck-billed platypus evolved. Why is it that it evolved in Australia and nowhere else? Well there are many examples of species extremely well-adapted but no parallel. Things like the chameleon, elephants, giraffes, many types of plants. Many evolutionary singletons. In fact, humans are an evolutionary singleton. If we are so well adapted to our environment, why didn&rsquot something like us evolve anywhere else in the world? Why didn&rsquot they evolve on Madagascar or in South America where monkeys colonized 40 million years ago?

And so this is the counterpart to the argument of evolutionary determinism and convergence. We could probably make a list just as long of species that have not converged. And so in many cases species &ndash in many cases evolution seemed not to be deterministic. That problems posed by environment may elicit different evolutionary solutions.

Human beings tend think that we—as a species—are very special. We dominate this planet that we're on, mostly due to our collective intelligence and ability to adapt to this particular climate. But Harvard biologist Jonathan B. Losos has an interesting theory that since there are so many Earth-type planets in our galaxy alone it's possible that there's some humanoid looking (at least in the bipedal sense) creatures out there, too. In fact, he posits, they might not even be that far off from the kind we're used to seeing in Hollywood movies. But he also dips into convergent evolutions, and presents the opposite side of the argument: evolutionary singletons. If you're interested in learning more, Jonathan's new book is called Improbable Destinies: Fate, Chance, and the Future of Evolution.

Chapter 32-3 Reading Guide

1. Carolus Linnaeus named our order Primates, which means ___________________ in Latin.
2. Primates have binocular vision, a well-developed ____________________, long fingers and toes, and arms that can _________________ around their shoulders.
3. ________________________ enabled many primates to run along tree limbs and swing from branch to branch.
4. Many primates have a flat face, so both eyes face forward with overlapping fields of view which gives primates excellent ____________________________ vision.
5. Humans and other primates ______________________________________ from a common ancestor that lived more than _______________ years ago.
6. ________________________alive today are small, nocturnal primates with large eyes.
7. Humans, apes, and most monkeys belong to the group called _____________________.
8. The anthropoids are divided into two main branches called the _______ _____________ monkeys and the _______ _____________ monkeys.
9. New World monkeys have a long, ____________________________ tail.
10. The skull, neck, spinal column, hipbones, and leg bones of early hominid species changed shape that enabled later species to ________________________________.
11. Define bipedal: ____________________________________________________________________
12. Define opposable thumb: ___________________________________________________________
13. The difference in Homo sapiens brain size results from an expanded ___________________.
14. Almost ________ of all known hominid species have been discovered in the last 20 years.
15. The best known species is Australopithecus afarensis - from a remarkably complete female skeleton nicknamed ________________.
16. Most ________________________ now place Paranthropus on a separate, dead-end branch of our family tree.
17. Hominid evolution did not move in ____________________________transformation.
18. Homo habilis was found with tools made of ________________ and __________ in several waves.
19. Paleontologist are unsure exactly __________________ and _________________ Homo sapiens arose.
20. Describe the "multi-regional" model. ______________________________________________________.
21. Describe the "out-of Africa" model. ________________________________________________.
22. Modern humans involves two main groups, they are H. ____________________
and H. ____________________________.
23. Neanderthals disappeared around __________________________years ago leaving our species the Earth's only hominid.

24. Use Fig 32-16 to describe the parts of the human and gorilla skeletons.

1. Which of the following is NOT a characteristic of most primates?
a. opposable digits b . well-developed cerebrum c . cloaca d . binocular vision

2. An example of a prosimian is the:
a. spider monkey b. lemur c. baboon d . orangutan

3. The fossil "Lucy" was a:
a. Australopithecus afaransis b . Homo habilis c. Homo sapiens d . Neanderthalis

4. A prehensile tail is one that:
a. is used for balance b . is absent or missing c. can wrap around branches d . is very short

5. Bipedal locomotion is an important adaptation because it allowed hominids to:
a. move faster b . communicate better c. climb trees d. use tools

How did this spider evolve to mimic exactly a human face and arms? - Biology

The term "Chit" (https:/˾˼it_(consciousness)) was introduced by The Upanishads for referring to consciousness˺wareness long before any of the modern philosophers did so.

On a separate note, I am interested in comparative theology (traditions in general) and the link you mentioned seems very interesting, thank you

---- Edit: For context: grew up in the middle east and living in California now, studied a ton about middle eastern theology and western theology, would love more resources on the east

The best explanation I've heard is that consciousness is an emergent property. The components are easily understandable but their complex interactions become increasingly hard to understand the more components you add.

Also, humans love to think they are special. And in some certain way we are. We are a big step of the evolutionary process of life. Usually, once such a big step happens, the first species (group) which figures it out becomes incredibly successful. E.g. the first plants that managed to live outside of water pools could colonize the barren landscape because there was no competition. Usually after such a step, this incredibly successful species then drifts and diversifies into multiple different sub-species and after a while there is a large ecosystem of species. We humans have discovered intelligence and now believe we are special, but in a few hundred years there'll likely be many types/kinds of intelligent structures we've built (not neccessarily our "biological" descendants, but this distinction matters little to life itself, which has a multitude ways of creating "biological" descendants anyways including things that don't involve any descendants at all like bacterial conjugation). Some of those structures we'll regard as conscious, others we won't. Consciousness will also vary in type and form, just how there are different ways for plants to vary in type of form. We are that first moss that colonized the lands. If you told that moss how plants could look like in 2020 (and it would understand the question), it would probably react similarly as people do to the Chinese Room argument.

No one can explain their own consciousness, so explaining someone else's consciousness isn't even ready to be discussd.

I suppose you’d get the hard-problem of matter if that was the case? Or wouldn’t you? It seems that idealism doesn’t run into the same problem. It’s easy to see how matter could simply be simulated in consciousness (we feel that every day). Especially if individual consciousnesses are simply child processes of a parent consciousness. But it’s harder to see how consciousness comes from matter.

> It’s easy to see how matter could simply be simulated in consciousness (we feel that every day)

And we are incorrect or imprecise in these simulations all day, every day. For the physical world to depend on our consciousness (and not the other way around), it would have to be a lot more chaotic. The earth orbited the sun when humans believed otherwise, even when there were no humans to think one way or the other.

>A program . knows where to put the symbols and how to move them around, but it doesn't know what they stand for or what they mean.

At a certain level of complexity, it must "know what they stand for or what they mean" in its encoding of how to move them around in order to move them around correctly.

Edit, references to refutations of Chinese Room argument:

Hofstadter, D., 1981, ‘Reflections on Searle’, in Hofstadter and Dennett (eds.), The Mind's I, New York: Basic Books, pp. 373–382.

"Margaret Boden (1988) raises levels considerations. “Computational psychology does not credit the brain with seeing bean-sprouts or understanding English: intentional states such as these are properties of people, not of brains” (244). “In short, Searle’s description of the robot’s pseudo-brain (that is, of Searle-in-the-robot) as understanding English involves a category-mistake comparable to treating the brain as the bearer, as opposed to the causal basis, of intelligence”. Boden (1988) points out that the room operator is a conscious agent, while the CPU in a computer is not – the Chinese Room scenario asks us to take the perspective of the implementer, and not surprisingly fails to see the larger picture."

That's a very good question, what is the first thing our evolutionary ancestors ever did, the first thought they ever had that made them different from all other species on the planet and deemed us sentient?

Or is the question of consciousness purely a philosophical one? since we can't really define the difference between humans and other species? Or can we?

Am I missing something? The difference is genetics, manifested via neocortex and thumbs.

The question isn't purely philosophical though, as there are entire fields devoted to the topic (cognitive sciences, areas of neuroscience, areas of ai research)

Personally, I subscribe to something along the lines of attention schema theory and panpsychism, and the last time I mentioned this on HN, lots of people agreed with this notion: the state of physical imbalance is, in mathematical terms, both sufficient and necessary for consciousness to evolve. (So if there is an imbalance in the realm of electromagnetic forces on some atom, the atoms 'urge' to adapt is what we describe as consciousness, albeit we usually experience the same phenomenon from a vastly more complex and abstract viewpoint (through the attention-mechanisms of our brain))

May I ask why? Given there are single-cell-organisms which display complex, intelligent behaviour [1]?

Where do you draw the line, and why? Are lobsters with their 18 'neurons' conscious to you? Because they look very conscious to me, although I'm biased (since electromagnetical imbalance is a sufficient explanation for consciousness in my eyes)

^ there's lots more to this than this single link. For example, I've read about single cell organisms that build shelter for themselves, not to mention 'the blob' (not sure if the ARTE-documentation was translated to english)

I don't know what consciousness is but I'm confident that it's more than just a page of if-then-else statements.

Are you? I'm not :/ I don't know what consciousness is either (if it is anything), but it doesn't seem unreasonable that it would be a spectrum. That the bottom of the spectrum would be as simple as "a page of if-then-else statements" doesn't seem particularly wild

The fact that millions of students taking intro CS courses haven't generated consciousness as part of their homework assignment leads me to believe that consciousness is a bit less trivial than a page of if then else statements.

Like all animals, we share a common ancestor with insects. At what point do you imagine our ancestors evolved this property that you imagine insects lack?

You personally began life as a single cell, which rapidly multiplied. At what point during your embryogenesis or subsequent development do you believe you gained the property of consciousness?

Would you claim that sub-atomic particles have consciousness? If not, and if you accept that humans have consciousness, then there are two options:

1) The step occured somewhere between sub-atomic particles and humans, so why not somewhere between insects and humans?

2) Consciousness is gradual, in which case I wouldn't be surprised if an insects consciousness is closer to a sub-atomic particle's consciousness than to a human's consciousness.

It makes no sense to say an atom has a little bit of temperature.

These are emergent properties that describe the interactions and interworkings of many many individual components.

It's not necessary that elementary particles have a "little bit" of consciousness. They also don't have any temperature, it not "a little" but undefined. It could be that you can only apply the concept of consciousness to sufficiently complex systems.

It reminds me of how some ancient Greeks felt there was a contradiction in 2 being large when compared to 1,but small when compared to 3. How can 2 possess the quality of smallness and largeness at the same time? Perhaps it has some smallness in it and also some largeness? Today we would say small and large are relative terms that apply to two things, it's a function that takes two inputs. They didn't have a solid grasp on concepts that exist in the relations between objects instead of them residing in the objects. I think today's consciousness debate is analogously misguided.

To be clear, when I say "closer to a sub-atomic particle's consciousness", I mean "not conscious at all". Hmm, I admit, that sentence could be misunderstood. Sorry, that was my fault.

How could that be what you meant? You laid out 2 options, and your corrected option 2 is the same as your option 1.

I don't get what you're saying. My "corrected" option 2 means that consciousness is a spectrum, that consciousness is not a binary property. A human is more conscious than a chicken, which is more conscious than an insect, which is more conscious than a bacterium, which is not conscious at all.

The more human something looks, the more plausible it seems that the being may be conscious.

But this begs the question of what consciousness is, and is not a scientific approach.

1) The step occured somewhere between sub-atomic particles and humans, so why not somewhere between sub-atomic particles and insects?

2) Consciousness is gradual, in which case I wouldn't be surprised if an insects consciousness is closer to a human's consciousness than to a sub-atomic particle's consciousness.

So we're back to the starting point of. nobody really has a clue what we're talking about :)

Did he? or did he begin at the point when that single cell multiplied into a sufficient number of properly organized cells?

That's what I take OPs argument to be, and you haven't provided any evidence as to why that isn't the case.

If you want to claim that an insect has consciousness or that a single cell does as well, why would you draw the line at a single cell? What would you say to someone who would claim that a virus has consciousness, or a ribosome? Why can't rocks be conscious?

At what number of cells do you figure consciousness exists? Call that N.

How does the addition of cells beyond N-1 imbue consciousness?

Sure, you could opt for the scientific version of panpsychism, where we attribute a property that we call consciousness purely by analogy to any system with some physical properties. But that still leaves you with the hard work of (a) proving that that property has anything to do with what we normally understand as consciousness (qualia, inner voice, etc.), and (b) defining the point/range where a system has enough panpsychism-consciousness to be considered conscious in the regular sense - e.g. at what size˺ge does a human have its first experience of thought? When the first neurons differentiate? When it is born? Later? Panpsychism could be a way to give an answer, but you still need to actually quantify this.

Of course, spiritual/religious panpsychism doesn't have this problem, it can posit that the soul should exists even outside of a physical body, that electrons can feel love etc. It is not provably wrong, but it is also outside the realm of what we can scientifically study, at least for now.

If you define consciousness as "something a child has that a sperm doesn't have" you are muddled up right at the start -- maybe thumbs are the essence of consciousness.

My point is that panpsychism seems to me to be using definitions to try to hide away the fact that it can't actually answer the questions of consciousness that we are really interested in any more than brain-based theories can.

I can well define "consciousness" formally as anything you like, even as something that vaguely intersects with the common-sense definition, like the information schema people did. But the fact of the matter is that we first have to understand consciousness, the vague common-sense concept, and only after we understand it can we give a precise formal definition that is actually useful.

Otherwise, it would be like defining the mass of an object to be the volume of an object - there is some overlap, and it is a perfectly formally defined, but it's just not the right definition for what you want to explain.

Let me ask you - do you believe that when a photon in the red wavelength hits an electron, the electron "sees red" in the same sense that you "see red" when that same photon hits your retina? What about your retina itself? Does it "see red" in the same sense that you do?

Consciousness of a physical system A is the difference between the behavior of A and the behavior of a system Aavg, that has the same content as A, but mixed randomly (think water and organics of the right weight and proportion simply mixed in a barrel).

This apparently breaks when you start using tools though.

Also, this definition does nothing to capture the difference between a philosophical zombie and a human, or help us tell if there is such a difference.

As for LHC, it actually needs quite a lot of people to be "conscious". E.g. to be powered and able to operate, so it makes sense, that, as an organization, it is more conscious than you are.

On the philosophical zombie I don't believe there's any difference in consciousness to a human, and the definition matches that idea.

Now Iɽ challenge anyone to give a better definition in terms of the number of examples contradicting it.

that is not very clear to me, care to explain how we know dogs have consciousness?

Spend enough time with dogs, and it becomes hard work explaining away that they are conscious, and most of the arguments you would come up with could be used to explain away that your neighbour is conscious, too.

So what we label “consciousness” is the ability to turn off the connectedness thing. We see ourselves as present and everything else as abstract or distant.

I think it’s evolutionarily adaptive, because the insect doesn’t _really_ care if it’s eaten by the flower. It’ll recoil from stress but it won’t fight to continue to exist with the same fervor that a “conscious” creature will.

But the irony for many of us is we are on a journey to rekindle that connected feeling. A major goal of life for some is to shed the lie of individualism and keep in mind the truth we knew before we became “conscious”—that we don’t really exist separately from the world around us. We are part of thousands of collective consciousnesses and we can only perceive the world at all through those collective eyes.

What I conclude from your statement is that you've never watched a nature documentary in your entire life.

Seems to me that this fly doesn't really consider itself a part of the spider web, and it very much cares whether it'll be eaten by the spider. It also seems to put up quite the fight. By your theory, that would mean the fly is conscious.

But. have you ever been in fight or flight mode? Subjectively it doesn’t feel like consciousness to me, it’s more a form of blacking out.

I’m not suggesting that “human consciousness“ is what allows us to recoil. I’m saying it adds another layer of survivalism on top of normal organism survival. It allows someone to move their family across an ocean, or spend your life building rockets to get off Earth.

Like, I don’t think Elon musk would be trying to get to Mars without his human consciousness telling him not just that humans are unique and distinct from the world, but that he personally is unique and distinct from the world.

And I guess I’m saying there’s another form of “consciousness” which I guess I have to call “life consciousness” to differentiate it from this “human consciousness” and that the differentiating factor that human consciousness feels separate from other consciousnesses.

And that was an evolutionary advantage for us apes and our survival.

Definitely not suggesting it’s the only way an organism fights for its survival.

He introduced me to the ideas in this paper that he induced from his own observations of his “mystical” experiences.

It is fascinating to realize these self models exist in a wide variety of animals and the modeling of others is what makes some animals different.

Yuval Harari argues that Homo sapiens took over all other Homo species because of the development of “myth” which may be related to the Hyperactive attribution of consciousness referenced in the article. Humans cooperate at scale much better than any other species (but also fight at scale more aggressively) because we can communicate about abstractions.

Very interesting inter-related ideas.

There is actually an immense amount of meditation on this very notion of an internal model, antecedent to the modern concept of consciousness we've been discussing since Kant, which guides a life form, from Aristotle down to St. Thomas Aquinas. See Daniel Heller-Roazen's "The Inner Touch: Archaeology of a Sensation"

That agrees with my guess that attribution to others came first, and our own is an accidental byproduct:

Secondly, even if the finding is correct, it gives no information about which function came first. It is consistent both with the idea that ɼonsciousness is empathy⾬tor modeling applied to the self' and with the idea that ɾmpathy⾬tor modelling is consciousness applied to other actors'.

In general, it is very hard to guess evolutionary timeliness from present structures where we have no idea of the genetic encoding of the current structures.

"In the AST [. ] was further adapted to model the attentional states of others, to allow for social prediction. Not only could the brain attribute consciousness to itself, it began to attribute consciousness to others."

On the face of it this AST theory would nicely support Susan Blackmore's work on the `meme`.

Recall Dawkins first proposed the meme, because he thought the gene was such a powerful mechanism there must be other similarly algorithmic mechanisms in nature.

In her 1999 book on the subject Blackmore proposed the theory `imitation` is at the heart of the evolution of human theory of mind

". if you want to know whether that huge male gorilla is likely to attack you if you try to mate with this attractive female, you should try to imagine what you would do in the same situation." (Blackmore, 73.3)

"ɺrms races' are common in biology, as when predators evolve to run ever faster to catch their faster prey, or parasites evolve to outwit the immune systems of their hosts." (Blackmore, 74.2)

"The turning point was when early hominids began to imitate each other. The origins of imitation itself are lost in our far past, but the selective (genetic) advantage of imitation is no mystery. [. ] If your neighbor has learned something really useful - like which foods to eat and which to avoid [. ] it may pay (in biological terms) to copy him. You can then avoid all the slow and potentially dangerous process of trying out new foods for yourself." (Blackmore, 75.3)

"I suggested imitation requires three skills: making decisions about what to imitate, complex transformations from one point of view to another, and the production of matching bodily actions. These basic skills, or at least the beginnings of them, are available in many primates and were probably available to our ancestors of 5 million years ago. Primates have good motor control and hand coordination, and good general intelligence which would enable them to classify actions and decide what to imitate. Some of them can imagine events and manipulate them mentally [. ] and, most notably, they have [social intelligence] and the beginnings of a theory of mind." (Blackmore, 75.5)

Seems this AST theory would offer Darwinian continuity and fill gaps in the qualitative theories of mind between other organisms and the exceptional human condition.

Blackmore, Susan. The Meme Machine. Oxford, UK: Oxford University Press. (1999)

Dawkins, Richard. The Selfish Gene. Oxford, UK: Oxford University Press. (1976)

How did this spider evolve to mimic exactly a human face and arms? - Biology

Early Man

Sean D. Pitman, M.D.


Taking isolated similarities by themselves, the theory of evolution appears to be quite reasonable. to a point. However, it seems that too much weight has been placed on similarities without questioning the differences. To the embarrassment of many a very intelligent man and woman of science, overly confident conclusions and arrogant statements have been made based on such similarities that have, on occasion, turned out to be not only wrong, but painfully wrong. It is fine to hypothesize that similarities between different creatures are the result of common ancestry, but since such similarities have been and are often conflicting when compared with other features, it might be prudent to hold back a little when making conclusions about any sort of definite taxonomic classification model or even relationship. The conclusions that are drawn from the evidence are often and have often been very much exaggerated to fit personal beliefs and biases. Yes, even scientists have biases and favorite theories. No one, not even a scientist, likes to see a theory that has cost a great deal of money and much of one's personal time and effort, go up in smoke. So, some caution might be in order before even long established theories are accepted as the "gospel truth", especially when some of the most famous scientists in the field start to question their own life's work.

In considering the theory of human evolution it is interesting to note that some very well known scientists have actually suggested that the line of human evolution is far from clear. For example, in 1990, Richard Leakey himself said that, " If pressed about man's ancestry, I would have to unequivocally say that all we have is a huge question mark. To date, there has been nothing found to truthfully purport as a transitional specie to man, including Lucy, since 1470 was as old and probably older. If further pressed, I would have to state that there is more evidence to suggest an abrupt arrival of man rather than a gradual process of evolving." 10 Mary Leakey also said pretty much the same thing just before her death at the age of 83. Although Leakey was convinced that man had evolved from ape-like ancestors, she was equally convinced that scientists will never be able to prove a particular scenario of human evolution. Three months before her death, she said in an interview, "All these trees of life with their branches of our ancestors, that's a lot of nonsense." 60

Biases are of course part of human nature. No one is immune from bias. However, bias should at least be admitted. As it is, popular sciences often refuse to admit that there are significant limitations to the evolutionary interpretations that are given out to the public as "gospel truth." Consider the evidence for yourself and judge if popular science has not and is not overstepping itself when it comes to its conclusions on "Early Man."

Piltdown Man -- Eanthropus dawsoni or "dawn man." Discovered in 1912 by Charles Dawson, a medical doctor and amateur paleontologist. Dawson found a mandible and a small piece of a skull in a gravel pit near Piltdown England. The jawbone was ape-like but the teeth had human characteristics. The skull piece was very human-like. These two specimens were combined to form dawn man, which was supposedly 500,000 years old. However, the whole thing turned out to be an elaborate hoax. The skull was indeed human (about 500 years old) but the jaw was that of a modern ape whose teeth had been filed to look like human wear. The success of this hoax for almost 40 years is pretty impressive. However, had the original bones been available for study, this hoax would probably not have continued for as long as it did. It was not until 38 years after the bones had been "found" that the hoax was exposed. In 1953 Kenneth Oakley, Joseph Weiner and Wilfred Le Gros Clark exposed the fact that Piltdown Man was a hoax. 1

Of course many scientists love to predict the discussion of Piltdown Man by those who are doubtful of evolution. But why shouldn't the Piltdown Man hoax be discussed? The success of the Piltdown Man hoax gives us an interesting look into human nature. It cannot be denied as a very embarrassing hoax that tricked even the scientific community for decades. It is readily admitted that many scientists believed in Piltdown Man wholeheartedly and made some rather foolish statements concerning the meaning of this "find." It is also admitted that Piltdown Man's general acceptance as a "missing link" was due to the fact that it matched the prevailing opinion of the time as to what such as missing link would look like. Of course, the argument is that many scientists of the day did not think too much of Piltdown Man since many did not think that the cranium and the jaw were from the same creature. But still, it is interesting to note that no one suspected the hoax despite "close inspection" of the specimen for almost 40 years. Other arguments contend that the differences from other fossil hominids are said to have turned Piltdown Man into a puzzling anomaly well before the hoax was discovered and, that by the time the hoax was revealed, most scientists were rather relieved to be finally rid of Piltdown Man. Even if this is true, the success of such an apparently obvious hoax seems quite impressive indeed.

So obviously, the point of including the Piltdown Man hoax in this discussion is to show that even scientists are, or at least have been, capable and possibly even willing to overlook something if it matches their preconceived ideas. (Back to Top)

Nebraska Man -- Hesperopithecus haroldcookii was discovered in 1922 in the Pliocene deposits of Nebraska by Mr. Cook and made famous by Henry Osborn of the American Museum of Natural History. There was an attempt to use this tooth at the Scopes "monkey" trial in 1925 as evidence of the animal ancestry of man. However, it was declared inadmissible by the judge. Even so, since William Jennings Bryan, former Secretary of State and a special prosecutor in the case, was himself from the state of Nebraska, Osborn chided him about Nebraska Man in the press: " The earth spoke to Bryan from his own state of Nebraska. The Hesperopithecus tooth is like the still, small voice. Its sound is by no means easy to hear ----. This little tooth speaks volumes of truth, in that it affords evidence of man's descent from the ape." 10 An illustration of Nebraska Man and his wife was published in the Illustrated London News (see illustration, printed June 24, 1922) . . . All from a tooth! When other parts of the skeleton were found in 1927, it quickly became clear that it was nothing more than the tooth of an extinct pig (peccary)! 2

In defense of the scientists of the day, many like to point out that this drawing was done for a non-scientific popular magazine. It is often claimed that few scientists, including Osborn, recognized Nebraska Man as anything more than an advanced primate of some kind. It is also claimed that Osborn specifically avoided making any extravagant claims about Hesperopithecus being an ape-man or any sort of human ancestor. To support this contention, Osborn is quoted as saying, "I have not stated that Hesperopithecus was either an Ape-man or in the direct line of human ancestry, because I consider it quite possible that we may discover anthropoid apes (Simiidae) with teeth closely imitating those of man (Hominidae). Until we secure more of the dentition, or parts of the skull or of the skeleton, we cannot be certain whether Hesperopithecus is a member of the Simiidae or of the Hominidae." 41 The fact of the matter is, however, that Osborn did believe that the Hesperopithecus tooth was clear evidence of human evolution from apes. If he did not believe this, then why did he chide Bryan by saying, " This little tooth speaks volumes of truth, in that it affords evidence of man's descent from the ape."? Of course, in retrospect, this statement of Osborn looks rather silly, seeing as how " Hesperopithecus" turned out to be nothing more than the tooth of a pig.

However, even if Osborn made some foolish statements about Nebraska Man, the claim is that most other scientists of the day did not even think that the Nebraska Man tooth was from a primate at all. In fact, the tooth was generally dismissed and had a negligible effect on the scientific thinking of the day. This is a strange conclusion considering the fact that a published picture of Nebraska Man in a popular and "respectable" news magazine did not raise very much objection from the scientific community of the day. The reply to this argument is often an appeal to a disclaimer that was published below the picture detailing the speculative nature of the picture.

"Mr. Forestier has made a remarkable sketch to convey some idea of the possibilities suggested by this discovery. As we know nothing of the creature's form, his reconstruction is merely the expression of an artist's brilliant imaginative genius. But if, as the peculiarities of the tooth suggest, Hesperopithecus was a primitive forerunner of Pithecanthropus, he may have been a creature such as Mr. Forestier has depicted." 42

I dare say that this disclaimer comment did not disclaim enough! The comment itself is very suggestive of the prevailing notion that Nebraska Man was in fact an ancestral hominid. That is a very far cry from an ancestral pig. Osborn himself commented on Forestier's drawing by saying:

"Such a drawing or 'reconstruction' would doubtless be only a figment of the imagination, of no scientific value, and undoubtedly inaccurate." 43

Little did Osborn know exactly how inaccurate it would turn out to be.

Beyond this, few understand the racially motivated nature of Osborn's ideas. Osborn firmly believed that certain human races were evolutionarily superior to other races.

"The Negroid stock is even more ancient than the Caucasian and Mongolian, as may be proved by an examination not only of the brain, of the hair, of the bodily characters, such as the teeth, the genitalia, the sense organs, but of the instincts, the intelligence. The standard intelligence of the average adult Negro is similar to that of the eleven-year-old youth of the species Homo sapiens ." 76

Consider such statements in light of the fact that Osborn's "intelligence" led him to use a single tooth as clear evidence of the evolution of humans from apes - a tooth which was later shown to be nothing more than a pig's tooth!

Many try to play down the Nebraska Man discovery and the influence that it was given by science and popular culture. However, the amazing thing is that the Nebraska Man tooth got any attention whatsoever and that such extravagant claims were ever made for it by anyone as respectable and intelligent as Osborn was. (Back to Top)

Getting it in the Right Ballpark - Sort of . . .

Ramapithecus lufengensis-- Ramapithecus, thought by popular scientists to have lived between 12 and 14 million years ago, was first discovered in southwest Kenya by Louis Leakey in 1932. At that time, all that was found were a few teeth and some fragments of the upper jaw or maxilla. Leakey assembled these fragments so that they fortuitously resembled the parabolically arched shape of a human jaw (apes have a more U-shaped form).

Because of this human-like maxillary shape and what were thought to be "human-like" teeth characteristics, this creature was long believed to be the first branch from a line of apes that eventually evolved into modern humans. Many drawings in various scientific publications, textbooks, and newspapers, show Ramapithecus walking pretty much upright based on these relatively few fragments of maxilla and a few teeth. One might think that the lesson of Nebraska Man would be remembered . . . but they weren't. Popular scientists through the late 1970s continued to actively promote Ramapithecus as one of the early human ancestors.

Noted scientist Dr. Elwyn Simons stated confidently, "The pathway can now be traced with little fear of contradiction from generalized hominids -- to the genus Homo." The importance of Ramapithecus as an early ancestor of hominids is evident in this comment by Simons in Time Magazine (Nov. 7, 1977):

" Ramapithecus is ideally structured to be an ancestor of hominids. If he isn't, we don't have anything else that is." 10

Interesting statement . . . But, from what evidence were these conclusions drawn in the first place? Once again, a few teeth and a portion of maxilla. From these few fragments many drawings have been made of Ramapithecus walking upright? Go figure?

Of course, not everyone was so confident. That is why t he almost exuberant confidence of Simons and his peers in the human ancestry of Ramapithecus is more than a bit surprising. For example, a study by Dr. Robert Eckhardt, which appeared in an earlier issue (1972) of Scientific American seemed to be quite problematic. 11 What Eckhardt did was to take 24 different measurements from the teeth of two species of Dryopithecus (a fossil ape) and one species of Ramapithecus. He compared the range of variation of these measurements with that of similar measurements taken from a population of modern chimpanzees. What Eckhardt found was quite interesting indeed. He found that there is greater variation in the teeth among living chimps than there is between Dryopithecus and Ramapithecus. This is significant because Ramapithecus was judged to be an early hominid primarily on the basis of itsteeth. Eckhardt concluded: " There is no compelling evidence for the existence of any distinct hominid species during this interval (pliocene 14 myo), unless the designation hominid means simply any individual ape that happens to have small teeth and a corresponding small face."

Then, i n 1976, renowned secular anthropologist Richard Leaky had this to say: "The case for Ramapithecus as a hominid is not substantial, and the fragments of fossil material leave many questions open." 9 Given what followed next, I'd say this is yet another huge understatement.

Despite this physical evidence, the apparently overwhelming desire to see the world in a certain way allowed most mainstream scientists to come up with all kinds of amazing things despite having so very little to work with. I mean really, they make CSI look like child's play! Despite the fact that only a few fragments of Ramapithecus were available, David Pilbeam, formerly at Yale and now at Harvard University, and Elwyn Simons, Duke University, both leading paleoanthropologists, strongly championed Ramapithecus as an early hominid, a creature in the direct line leading to the evolution of humans. (Simons E. L., Ann. N. Y. Acad. of Sci, 1969, 167:319 Simons E. L., Sci. Amer, 1964,. 211(1):50 Pilbeam D. R., Nature, 1968, 219:1335 Simons E. L. & Pilbeam D. R., Science, 1971, 173:23).

Then, in 1977, a little problem surfaced for Ramapithecus - a full jaw (mandible) was discovered. This jaw bone was U-shaped, not parabolically shaped.

Zilman and Lowenstein attempt to explain the reason for the earlier thinking of most of the world most prominent paleoanthropologists :

" Ramapithecus walking upright has been reconstructed from only jaws and teeth. In 1961 an ancestral human was badly wanted. The prince's ape latched onto position by his teeth and has been hanging on ever since, his legitimacy sanctified by millions of textbooks and Time-Life volumes on human evolution." 10

After the discovery of the full jawbone in 1977, David Pilbeam admirably recanted his earlier views commenting that, "A group of creatures once thought to be our oldest ancestors may have been firmly bumped out of the human family tree. Many paleontologists [including David Pilbeam] have maintained that Ramamorphs are our oldest known ancestors. These conclusions were drawn from little more than a few jawbones and some teeth. Truthfully, it appears to be nothing more than an orangutan ancestor." 3

Isn't it interesting that Pilbeam was so convinced before the jawbone discovery that Ramapithecus was indeed an early human ancestor, despite the very limited material, when only after the jawbone discovery does he seem to recognize the limited nature of what he really did have to work with.

Currently, the general view of science is that Ramapithecus was nothing more than an ancestor of the modern orangutan or even of a third lineage which has no modern survivor. 70 Note the following conclusion published in a 1981Science Digest article : "A reinterpretation of this jaw now suggests that Ramapithecus was an ancestor of neither modern humans or modern apes. Instead, Pilbeam himself thinks it represents a third lineage that has no living descendants."

What is interesting though is that even in relatively recent times Ramapithecus was widely considered an evolutionary link between apes and man. This opinion was strongly held and taught as unquestionable fact in public schools for many years, and is still being taught in some places based on what is now thought to be, not so many years later, very poor evidence. Such is the power of a prevailing paradigm to make one believe in just about any story that "fits" regardless of the quality of the evidence presented. (Back to Top)

Australopithecus africanus -- The word "Australopithecus" means "southern ape." This name is used because the first fossils were found in South Africa. Dr. Raymond Dart, professor of anatomy at Witwatersrand University in Johannesburg, was the first to study these fossils. In 1924 at Taung in South Africa, Dart discovered a fossil skull consisting of a full face, teeth and jaws, and an endocranial cast of the brain. The brain size was 410cc. Its age is currently felt to be around two to three million years old. Dart was convinced that some teeth were man-like and thus concluded a transition between apes and man. His opinions on the matter of this particular skull were largely scorned by the scientists of this time (1924) who considered it nothing more than a young chimpanzee (now considered to be about three years of age). The skull was soon known derisively as "Dart's baby." 10 Sir Solly Zuckerman, an expert on australopithecines, commented that, "There is indeed no question what the australopithecine skull resembles when placed side by side with specimens of humans and living ape skulls. It is the ape so much so that only detailed and close scrutiny can reveal any difference between modern ape and Australopithecus." 4 This opinion was generally held by scientists until the mid-1940's when similar skulls were found. Dart had made his discovery during the time that Piltdown Man was widely accepted as a human ancestor. With Piltdown Man's human cranium and apelike jaw, it was hard to reconcile it to the Taung Child. Then in the 1930's Peking Man became famous, again overshadowing Dart and his Taung Child. Although Dart gave up fossil hunting for some time, all was not lost.

Years after the discovery of the "Taungs child", as it is known today, Dart and Broom found other Australopithecines at Kromdraii, Swartkrans and Makapansgat. These finds of similar creatures seemed to vindicate Dart and Broom, and the scientific community again accepted their finds as they do today. These new fossil Australopithecines seemed to show two parallel lines of development, one being a small "gracile" (slender) type and the other a larger "robust" type. Much controversy has existed regarding these types and some investigators, including Richard Leakey, have concluded that they represent merely the male and female of the same species while others say the gracile form, which is believed to be older, evolved into the robust form. Today these animals are known as Australopithecus africanus and Australopithecus robustus respectively. The latter is clearly heavier, has more massive jaws, and a pronounced sagital crest. All these traits are typical of sexual dimorphism in male apes. What is also felt to be a more human trait is that foramen magnum (the opening in the skull above the attachment of the spinal column) in Australopithecines seems to be placed in an intermediate forward position between that of modern apes and man. Although not as far forward as in man, this more forward position is felt to indicate a more upright posture for the Australopithecines.

The australopithecines have often been found in association with other animals, such as baboons, and often show evidence of bashed-in skulls. Tools in the form of clubs, knives, and choppers have been found in association, as well as evidence of fire. It might be attractive to assume that the Australopithecines had been the hunters and butchers except that some of their skulls were broken in as well. Were they then the hunters or the hunted? An American journalist met up with Dart who convinced him that the Australopithecines were actually hunting one another. The journalist, Robert Ardrey wrote a book, African Genesis, which popularized the view of the "killer ape." This view was even used in the movie, "2001, A Space Odyssey." Although the view did reach a mild degree of popularity, it has since been widely discredited. 10 It does seem rather hard to imagine how such primitive creatures could actually make all those weapons and use fire as well. Not bad for a primitive man who is still not yet walking completely upright and has a head the size of a chimp (less than 500cc max).

Although modern scientists do generally accept that Australopithecines had a generally upright gait and human-like posture, this notion has not gone uncontested. Although evolutionists predictably discount Zuckerman's work, arguing that it is no longer accepted (further discussion of such arguments a few paragraphs below), one must still at least consider the fact that in the 1950s the famous British anatomist, Lord Solly Zuckerman, aggressively rejected the notion that Australopithecines are closely related to humans and completely discounted the notion that they walked upright like humans. Rather, Zuckerman suggested that they be classified as apes, not hominids (Evolution as a Process, 1954):

"There is, indeed, no question which the Australopithecine skull resembles when placed side by side with specimens of human and living ape skulls. It is the ape - so much so that only detailed and close scrutiny can reveal any differences between them".

As for the notion of "bipedal posture", Zuckerman said:

"In short, the evidence for an erect posture, as derived from a study of the inanimate bones, seems anything but certain."

A natomist Dr. Charles Oxnard of the University of Chicago, who's work modern evolutionists also reject (see below), claimed in a paper published in a 1975 edition of Nature that:

"Multivariate studies of several anatomical regions, shoulder, pelvis, ankle, foot, elbow, and hand are now available for the australopithecines. These suggest that the common view, that these fossils are similar to modern man, may be incorrect. Most of the fossil fragments are in fact uniquely different from both man and man's nearest living genetic relatives, the chimpanzee and gorilla (Nature 258:389).

Neither of these investigators, who have spent much of their professional careers studying the Australopithecines, believed that Australopithecines walked upright or that they were generally bipedal. Some have suggested that both Australopithecus africanus and robustus were simply an evolutionary dead end - not ancestral to man.

However, many evolutionists, such as those that frequent Talk.Origins, argue that, " Howell et al. (1978) criticized this conclusion [of Charles Oxnard] on a number of grounds. Oxnard's results were based on measurements of a few skeletal bones which were usually fragmentary and often poorly preserved. The measurements did not describe the complex shape of some bones, and did not distinguish between aspects which are important for understanding locomotion from those which were not. Finally, there is 'an overwhelming body of evidence', based on the work of nearly 30 scientists, which contradicts Oxnard's work. These studies used a variety of techniques, including those used by Oxnard, and were based on many different body parts and joint complexes. They overwhelmingly indicate that australopithecines resemble humans more closely than the living apes."

Perhaps the most significant problem with this argument (discussed in more detail below in the section on "Lucy") comes in the form of Fred Spoor's very interesting computed tomography scan (CT-scan) analysis (1990s) of the preserved inner ear canals of Australopithecus africanus and robustus.Inner ear canals are used to determine orientation in space. In other words, their orientation can be used determine the position of the head and posture. Spoor compared the canals of many living primates, to include humans, with many "hominid" fossils. As it turns out, the canals of Australopithecus africanus and robustus are most similar to the great apes - not modern humans. Spoor and his associates concluded that this finding was consistent with the idea that these creatures were at least partly arboreal and that they "did not walk habitually upright."

Of course, Spoor still believed them to be partly bipedal as well, but suggested that his findings proved that these "hominids" were not obligatory bipeds as humans are, but were instead part-time bipeds at best - certainly not nearly as accomplished at bipedalism as are humans. For example, they would have had a very hard time running on two legs - as is true for apes today. 44,65

Consider that this labyrinth evidence goes completely counter to several long-accepted assumptions based on much weaker morphologic characteristics. In fact, this evidence speaks directly counter to the position that H. habilis is a "missing link" - intermediate in the evolution of bipedalism between australopithecines and H. erectus - actually supporting the positions of Zuckerman and Oxnard. Spoor also found extreme differences in the labyrinthine morphology between SK 847 and Stw 53. These two specimens were both classified in the H. habilis species group. However, according to Spoor, SK 847 has a "modern-human-like labyrinth" while "Stw 53 relied less upon bipedal behavior than the australopithecines." 44,65

Talk about confusion! This CT-scan evidence is far more objective than the measurements done by Howell and his colleagues, and it throws their conclusions on their head where many of the previous notions of hominid evolutionary sequence and relationship are at best contradictory. These problems are so bad that perhaps we could write the Australopithecines off entirely as ancestral to modern man if were it not for the current love affair with an Australopithecine named "Lucy." (Back to Top)

Australopithecus afarensis " LUCY" -- In 1974, Donald Johanson discovered a half complete skeleton (Locality A.L. 288 Ethiopia's Awash Valley ) that he named after the Beetle's song "Lucy in the Sky with Diamonds" (LSD). The specimen was only 1.1 meters tall, estimated to weigh 29 kilograms and look somewhat like a common chimpanzee. A year later, thirteen similar skeletons were found.

In his book "Lucy, The beginnings of Human Kind," Johanson said: "I had no problem with L ucy. She was so odd that there was no question about her not being human. She simply wasn't. She was too little. Her brain was way too small and her jaw was the wrong shape. Her teeth pointed away from the human condition and back in the direction of apes. The jaws had the same primitive features." (see jaw illustration below)

However, what set Lucy apart for Johanson was that it appeared that she had a tendency to walk in an upright position. A monkey that could do this would, for Johanson, clearly be some sort of transitional form between apes and man. The reason for this belief is because Lucy's knee region seemed to match a lone fossilized knee joint that he had found a year earlier in 1973 (locality numbered A.L. 128/129). The earlier knee was from a creature that appeared to walk in an upright fashion. Even though it was located about 2 km away and in a lower strata from that of Lucy, the match between it and the knee region of Lucy seemed to indicate that both individuals walked mostly upright. The logic for this assumption is based on the fact that humans, because of wider hips than knees, have an angle between the upper leg bone (or femur), and the lower leg bone (or tibia). This

angle of the bones causes an angle of about 9 degrees to form in the knee joint at the junctions of the bones. An ape that walks on all fours does not have this angle. Lucy and the australopithecines have an angle of about 15 degrees. Since this larger angle is somewhat similar

to the human condition, the obvious assumption is that Lucy spent a lot of time walking upright. 21 There is just one more interesting fact though. Monkeys that climb trees (ie: orangutans and spider monkeys etc.) also have an angled knee joint like humans. It is the ground-dwellers that do not have the angle. So, what happens if Lucy tended to climb trees? Is there evidence that she did climb trees?

Dave Phillips (a paleoanthropologist) says that A. afarensis in general (Lucy's classification) has long upper limbs with an arm to leg length ratio of approximately 85%. The toe bones are also curved in an ape-like manner. This characteristic curve is not seen in human feet. This seems to indicate that A. afarensis did not habitually walk upright, but rather spent much of their time in trees. Also, studies of the other bones to include hands, skull (inner ears), and even the teeth indicate a fairly strong similarity to apes. 45

1. General anatomy of Lucy's shoulder blade was characterized as "virtually identical to that of a great ape and had a probability less than 0.001 of coming from the population represented by our modern human sample" (Susman et al, 1984, pp 120-121)

2. Lucy's shoulder blade has a shoulder joint which points upwards (Oxnard 1984, p334-i Stern and Susman 1983, p284) This would allow "use of the upper limb in elevated positions as would be common during climbing behavior" (Stern and Susman, 1983, p284). 5

3. Afarensis wrist bones are apelike. "Thus we may conclude that A. afarensis possessed large and mechanically advantageous wrist flexors, as might be useful in an arboreal setting" (Stern and Susman, 1983, p282).

4. Afarensis metacarpals [the bones in the palm of the hand] "have large heads and bases relative to their parallel sided and somewhat curved shafts an overall pattern shared by chimpanzees". This "might be interpreted as evidence of developed grasping capabilities to be used in suspensory behavior" (Stern and Susman 1983, pp 282-3).

5. The finger bones are even more curved than in chimpanzees and are morphologically chimpanzee-like. (Stern and Susman 1983, pp 282-4 Susman et al 1984 p. 117 Marzke 1983, p 198).

6. Afarensis humerus (upper arm bone) has features that are "most likely related to some form of arboreal locomotion" (Oxnard 1984, p.334-1 see also Senut 1981, p.282).

7. One of the long bones in the forearm, the ulna, resembles that of the pygmy chimpanzee (Feldsman 1982b, p.187).

8. Vertebrae show points of attachment for shoulder and back muscles "massive relative to their size in modern humans" (Cook et al 1983, p.86) These would be very useful for arboreal activity (Oxnard 1984, p 334-i).

9. "Recently Schmid (1983) has reconstructed the A.L. 288-1 rib cage as being chimpanzee-like" Susman et al 1984, p 131).

10. Blades of hip oriented as in chimpanzee (Stern and Susman 1983, p.292.) Features of afarensis hip therefore "enableproficient climbing" (Stern and Susman 1983, p. 290).

11. In 1987, Dr. Charles Oxnard (University of Western Australia) analyzed certain australopithecines (such as Lucy is classed as). He concluded that they were not ancestral to humans, but are instead an extinct form of arboreal ape. 6 Of course, this analysis was done before Lucy came on the scene and changed everything.

Emphasis added to the above statements to highlight the tree-climbing characteristics of Australopithecines.

So, it seems like Lucy really did not need or wish to do a lot of walking around on the ground. It seems more likely that she spent much of her time in trees. Since the angle of her knee joint is a key factor in turning her into a "missing link" in human evolution, what happens to this argument when one finds out that such an angled knee joint is owned by tree dwelling chimps? It it not something new. Where is the evolution here?

Of course evolutionists are well aware of these "standard creationist arguments." A common rebuttal is to argue that the authors of many of the comments I just quoted above are themselves believers in Lucy's role as a "missing link" between chimps and humans. Consider the following comments by Stern and Susman:

"In our opinion A. afarensis is very close to what can be called a "missing link". It possesses a combination of traits entirely appropriate for an animal that had traveled well down the road toward full-time bipedality . " "That bipedality was a more fundamental part of australopithecine behavior than in any other living or extinct nonhuman primate is not in serious dispute." ". we must emphasize that in no way do we dispute the claim that terrestrial bipedality was a far more significant component of the behavior of A. afarensis than in any living nonhuman primate." (Stern, Jr. and Susman 1983)

So, how can Stern and Susman believe that A. afarensis spent so much time running around on two legs after they just detailed many physical attributes of classic tree climbing behavior? Some of the reasons are as follows:

"The most significant features for bipedalism include shortened iliac blades, lumbar curve, knees approaching midline, distal articular surface of tibia nearly perpendicular to the shaft, robust metatarsal I with expanded head, convergent hallux (big toe), and proximal foot phalanges with dorsally oriented proximal articular surfaces. (McHenry 1994)

This is an example of interpreting the same characteristics in different ways. For example, the perpendicular tibia and angled knee joints that are "approaching midline" are seen in modern tree-climbing monkeys. The "robust" first metatarsal with an expanded head is also consistent with Stern and Susman's comment that the hand bones (and reasonable the foot bones as well), " have large heads and bases relative to their parallel sided and somewhat curved shafts, an overall pattern shared by chimpanzees." and that this, "might be interpreted as evidence of developed grasping capabilities to be used in suspensory behavior ." This might especially be true if the first digit was favored by Lucy to carry most of her body weight during suspension.

This is an example of picking morphological traits that agree with a favored hypothesis and forgetting about the ones that do not agree or even contradict the hypothesis of the day. For instance, fairly recent papers have been published that suggest that Lucy was in fact a "knuckle walker" like some apes living today. 38 Of course knuckle walking is a distinctly quadruped specialization characteristic that is quite different from bipedalism. The authors of this paper, Richmond and Strait, identified four skeletal features of the distal radius of living knuckle-walking apes, chimps and gorillas. What is interesting is that they found similar morphologic features on Lucy as well as on another australopithecine.

"A UPGMA clustering diagram illustrates the similarity between the radii of A. anamensis and A. afarensis and those of the knuckle-walking African apes, indicating that these hominids retain the derived wrist morphology of knuckle-walkers." 38

In an interview, Richmond stated that after they analyzed the wrist characteristics of living knuckle-walkers, he and Strait walked across the hall to check plaster casts at the National Museum of Natural History: "I walked over to the cabinet, pulled out Lucy, and shazam! she had the morphology that was classic for knuckle walkers ." 39 Of course Richmond and Strait still believe that Lucy walked upright despite these knuckle-walking features. They believe that these features are simply evolutionary remnants of past ancestor knuckle walkers but that Lucy herself was bipedal. Some suggest as evidence for this assumption that Lucy lacks certain knuckle-walking features. 39 Of course, there are modern knuckle-walkers that are also known to lack one specific feature or another, but they are still knuckle walkers. 38

It seems now that Lucy was quite an amazing creature. She not only had features of tree-climbing behavior and bipedalism, but now it seems like she has features of knuckle-walkers as well. So, which of these characteristics are the result of lifestyle and which ones are evolutionary carryovers?

Lucy becomes even more problematic when one considers her classic placement in evolutionary phylogeny. Lucy is thought to be an ancestor or early form ofA. africanus because of Lucy's more chimpanzee-like skull. The problem is that the foot bones and lower leg of an A. africanus specimen have been recently found. These foot and leg bones happen to be a lot more apelike than the hypothesized foot of Lucy. 40 Also, A. africanus does not have the knuckle-walking morphology that Lucy has. So, depending on what part of the body one concentrates on, one might be able to find evidence for just about any theory of locomotion that one wishes to find. Collard and Aiello, in an article for Nature, commented on this confusing phylogenic mess by saying:

"The work by Richmond and Strait further complicates the picture: it suggests that A. afarensis retained some knuckle-walking features, whereas A. africanus did not. It is no longer a case of the skull pointing to one set of phylogenetic relationships, and the postcranial skeleton (everything but the skull) to another. Rather, different parts of the postcranium may not support the same phylogenetic hypothesis." 40

The anatomy of the semicircular canals of australopithecines is also interesting. The semicircular canals are three small, loop-shaped structures in the inner ear, arranged roughly at right angles to each other. These structures are responsible for giving us our sense of balance by allowing us to orient ourselves with respect to a gravitational field. In the early 1990s, a scientist by the name of Fred Spoor decided to study these canals. He compared the canals of many living primates, to include humans, with some "hominid" fossils. He used a computerized tomography scanner (CT-scanner) to do this. His results were very interesting. The canals of Australopithecus africanus and robustus were most similar to the great apes. Spoor and his associates concluded that this finding was consistent with the idea that these creatures were at least partly arboreal and that they "did not walk habitually upright," but Spoor still believed them to be partly bipedal as well. Spoor believed that his findings proved that these "hominids" were not obligatory bipeds as humans are, but were instead part-time bipeds, and not as accomplished at bipedalism as humans are. 44,65 Consider Spoors following comments published in a 1994 issue of the journal Nature:

". . . A. africanus showed a locomotor repertoire comprising facultative bipedalism as well as arboreal climbing. The labyrinthine evidence is consistent with proposals that bipedalism in australopithecines was characterized by a substantial postural component [non-bipedal], and by the absence of more complex movements such as running and jumping.

. . . the similarity with the canal proportions in large cercopithecoids suggests that Stw 53 [Homo habilis - discussed below] relied less on bipedal behaviour than the australopithecines. Interestingly, similar observations were reached from an analysis of the postcranial bones of OH 62, a specimen that has been assigned to the same species as Stw 53 on the basis of similarities of their maxillary and dental morphology. Phylogenetically, the unique labyrinth of Stw 53 represents an unlikely intermediate between the morphologies seen in the australopithecines and H. erectus. . .

The specimen SK 847 has both been associated with H. erectus and H. habilis, in particular with Stw 53. The modern-human-like labyrinth of SK 847 is consistent with the attribution to H. erectus, and the extreme differences in labyrinthine morphology between SK 847 and Stw 53 make attribution of both specimens to the same species, on this evidence alone, highly unlikely. The specimen Sts 19 is part of the conventional A. africanus hypodigm, but has also been considered as a basicranium of early Homo. As the labyrinth of Sts 19 is very similar to that in the other three A. africanus specimens, and major aspects of its overall morphology, such as petrous pyramid orientation and basicranial flexion, can easily be accommodated in normal species variation . . ." 65

Note how this labyrinth evidence goes completely counter to several long accepted assumptions based on much weaker morphologic characteristics. In fact, this evidence speaks directly counter to the position that H. habilis is a "missing link" intermediate in the evolution of bipedalism between australopithecines and H. erectus. Note also the extreme differences in the labyrinthine morphology between SK 847 and Stw 53. These two specimens were both classified in the H. habilis species group. However, according to Spoor, SK 847 has a "modern-human-like labyrinth" while "Stw 53 relied less upon bipedal behaviour than the australopithecines." Also, how can Sts 19 have been considered as a "basicranium of early Homo" with a labyrinth "very similar to the other three A. africanus specimens"? I mean really, an early Homo would most certainly have had well developed bipedalism - right? How then can a specimen classified as "early Homo" have an inner ear labyrinth that is not distinguishable from creatures that did not have well developed bipedalism at all? I ask you, how objectively accurate a "science" can these classification systems be if they can be this far off so many times?

Consider also that perfectly formed human footprints have been found in solidified volcanic ash dating at around "3.6 million years" (See discussion on Ancient Footprints below). These footprints show no evidence of the curved tree-climbing bones of Lucy or of the ape-like toes of A. africanus. The footprints have a well shaped modern heel, strong arches, and a good ball at the base of the great toe. The great toe itself is in a straight line. It does not stick out to the side like an ape toe does. These footprints are in all respects indistinguishable from the footprints of modern humans, 23 and yet Johanson claims that Lucy-like creatures ( A. afarensis ) made these footprints since they are found in ash dated to be about as old or older than Lucy. But where is the evidence for Johanson's claims? The available evidence suggest that A. afarensis could not have made these footprints owning to the fact that they have curved toes. Despite this fact, Johanson continues to be a strong believer that A. afarensis made these footprints anyway. I ask, is this science. or wishful thinking?

It seems like the more is learned about Australopithecus, the more apelike and less like a "missing link" they appear. In fact, as recently as April of 2007, Rak et. al. found a portion of a jawbone of A. afarensis that matched the general appearance of gorillas (and Australopithecus robustus ) - a feature not shared by modern humans, chimpanzees, orangutans, and other primates. Rak argues that, "The presence of the morphology in both [ A. robustus ] and A. afarensis and its absence in modern humans casts doubt on the role of A. afarensis as a modern human ancestor." 75

Of course, only a very few stop to consider the possibility that perhaps there is no evolutionary relationship between humans and apes at all. Perhaps certain of these unique "traits" were designed specifically for particular creatures with particular needs? Perhaps humans did not evolve from apes after all? In any case, it seems like the evidence is far from being conclusively in favor of any particular evolutionary relationship. The unknowns are too great and too much subjective interpretation is required to draw any definite evolutionary conclusions from the fragmented and pieced together bones of Lucy and her cousins. One starts to wonder what evidence it would take to cause the smallest shadow of doubt to creep across the minds of some of these paleontologists as to the veracity of their beliefs?

One other interesting statement by Johanson concerns how he feels at least some of the individuals met their end: "The rapid burial of bones at Hadar, particularly those of the 'First Family,' are related to a geological catastrophe suggesting, perhaps, a flash flood. Bones are fragmented and scattered because individuals fell into a river, or were washed into a river, rapidly transported, broken up, and scattered. These are all products of a depositional process." (The 333, or the 'First Family' locality, as it is sometimes called, at Hadar, is situated stratigraphically between the Lucy site and the 1973 knee joint site.) 21

Homohabilis -- Homo habilis was discovered in 1959 by Mary Leakey and dated at about 1.8 million years old. What she found were some badly fragmented pieces of skull. Her husband, Louis Leakey, was not impressed at first. He commented that it was nothing more than a "damned Australopithecine". However, he quickly changed his mind when what appeared to be stone tools were found near the site of Homo habilis. The bones of many of these animals revealed that they had been butchered and deliberately broken for their marrow. Leakey decided, on the basis of this evidence, that his fossil had been a toolmaker and butcher and thus called him Homo habilis or "handy man." Most other investigators, however, were not comfortable with such an extremely primitive beast being a toolmaker. Like Australopithecus robustus, Leakey's "Homo habilis" had huge and very unhuman molars, a very small brain, and a large bony sagital crest on the top of its skull. Later, Leaky thought better of the whole idea of his "Homo habilis" as a tool maker and demoted him to the classification of Zinjanthropus boisei, which means East African man.

The skull of Zinj is especially robust, sometimes called, "hyper-robust". Notice, in the reconstruction of Zinj, the very wide zygomatic arches, which project forward in front of the nasal opening to form a dish-shaped face (like many apes today). These outward flaring arches provided space for huge temporalis muscles that are used for chewing. In other words, Zinj had a very powerful bite. Zinj's teeth are also massive, sometimes more than 4-times the size of modern human teeth. (Note that the mandible portion of the jaw in the reconstruction was not originally found with Zinj, but is based on subsequent finds of similar individuals).

Although Mary Leaky found Zinjanthropus, or "Zinj", it made Louis Leakey famous as a result of the publicity he received from the National Geographic Society through its magazine and educational films. The National Geographic Society financed Leakey's work and largely, through their publicity of Leakey and Zinj, paleoanthropology once again became both popular and "respectable" after a long period of disrepute following the Piltdown hoax. Today, Zinjanthropus is considered by everyone to be just another robust Australopithecine - just as Lewis Leaky originally said it was. 1 0

Australopithecines are considered by many to be hominids because they are believed to have been bipedal and thus walked upright. Until the 70s, the upright and bipedal posture was based on the position of the foramen magnum in the skull and very fragmentary finds of pelvis, limb and foot bones. Then, Richard Leakey found several more nearly complete remains that threw considerable doubt on the idea of an upright posture. In Science News Leakey concluded that, "The Australopithecines were long-armed short-legged knuckle-walkers, similar to existing African apes." 12

These setbacks did not stop Leakey. In 1964, he found four more specimens in Olduvai Gorge. These, he claimed, had bigger brains than Australopithecus and surely deserved to be classified as Homo habilis. Measurements of the cranial capacities were difficult since the skulls were so badly crushed. Nonetheless, it was concluded that they averaged 642cc, or 200cc larger than Australopithecus and he considered that enough to make them "Homo. " Several such finds are discussed blow.

OH 7 is a collection of 23 fragments of bone to include a jawbone and teeth thought to be from a male hominid who lived some 1.75 million years old. These fragments were also found at Olduvai gorge in Tanzania. The problem, like many of the rest of the other fragmentary evidence, is that there really isn't much to interpret here. And, what there is, looks much more like the ape condition than it does the human condition. Consider that the shape of the jawbone is the ape-like U-shape - not the parabolic human shape.

OH 24 is a pieced together skull of a "female" hominid thought to have lived some 1.8 million years ago. She was given the nickname "Twiggy", after the famous flat-chested British model, because of the compressed and flatted condition of the skull when it was first discovered with its fragments cemented together in limestone. When the hundreds of fragments were pieced together, the size of the brain case was quite large at just under 600cc. Since modern human brains can be this small, the finding of Twiggy, with such a large brain, was thought to be a very good missing link, and gave support to the rather weak classification of OH 7 as "Homo". Also note that more than 100 fragments of skull were not used in the final reconstruction of Twiggy.

KNM-ER 1813 is said to be an adult cranium from an individual who lived some 1.9 million years ago. Some have classified it as Homo habilis, but this classification is controversial. Donal Johanson said, ". . . we have opted to include KNM-ER 1813 in Homo habilis, following the classification of Bernard Wood. Richard Leakey . . . has recently avoided putting a taxonomic label on 1813 other than to say that it should not be called Homo habilis . . . ". 71 The skull capacity is a bit small than that purported for OH 24 (510cc for KNM-ER 1813 vs. just under 600cc for OH 24).

OH 62 has been interpreted as a partial adult skeleton from a hominid who lived about 1.8 million years ago. The initial find was a fragment of proximal right ulna (arm bone). After this, the search for additional parts of this skeleton was on - and quite successful. Over 18,000 fragments of bone and teeth were found over an area of about 40 square meters. Most were classified as non-hominid remains, but 302 fragments were "identified" as belonging to OH 62. I'd say that's quite impressive detective work!

The problem was that even with the 302 fragments available, they were too fragmented to build a cranial vault or skull with any "accuracy". However, portions of the right arm, including most of the humerous and parts of the ulna and radius, as well as portions of the left femur and most of the maxilla (32 original fragments) were reconstructed. From this reconstruction it is estimated that the adult OH 62 stood just one meter is stature - very short for a hominid ancestor. On top of this, OH 62 has very long arms compared to its legs, similar to the ape ratio today. The humerous-femur ratio of OH 62 is 95%, while in apes it is 100% and in modern humans it is 70%.

Such apelike proportions for Homo habilis were quite unanticipated - a bit of a shock actually. If H. habilis was to be considered an ancestor to H. ergaster/erectus by 1.6 million years before present, then not only would body size have to increase rather considerably, but the relationship between upper and lower limbs would also have to change quite dramatically. Would a mere 200,000 years be enough time for such changes to be realized? I mean really, from the evolutionist perspective, 200,000 years just isn't that much time. Even if such changes were possible, such differences between H. habilis and modern humans make it quite difficult to use H. habilis as any sort of convincing "missing link". In fact, the finding of OH 62 has only added to the confusion over how to interpret the very fragmented remains of these "early hominids".

So, obviously, n ot everyone was as enthusiastic as Leakey was about his new "handymen." For a time, Homo habilis was considered an empty taxon that was inadequately proposed. 10 Then, in 1972, very interesting skull fragments were unearthed by Leakey's field hand, Bernardo Ngeneo. This discovery was to shake up the world of paleoanthropology. Richard Leakey and his team had found the toolmaker his father, Louis Leakey, had long sought in vain. The fossilized bone fragments of this skull were found near Lake Turkana, Kenya. Leakey's wife, Meave (a palaeontologist), assembled the fragments to make a nearly complete skull minus the lower jaw (a human-like femur was also found a few kilometers away, but associated with the skull since they were both found within the same sedimentary layer). 66,67 The skull was named KNM-ER 1470 for its registration at the Kenya National Museum in East Rudolf.

The skull capacity was difficult to measure because of the condition of the assemblage, but was estimated to be around 800cc (later lowered to 750cc). This large cranial capacity was much larger than so-called ape-men skulls. Also, KNM-ER 1470 had only small eyebrow ridges, no crest, and a domed skull. These traits were thought to be more typical of the human condition. Indeed, it appeared to have at least four major human-like traits to include:

A high forehead with a dome-shaped cranial vault relative to the fairly flat and low forehead of australopithecines and modern apes

Lack of prominent brow ridges

A "flat" face lacking the usual "protruding prognathous" of australopithecines

As an extra - Associated femur and leg bones very similar to that of modern humans (found a few kilometers away in the same layer)

The problem here, of course, is that the original reconstruction started to be doubted, even by evolutionists, because it did not seem to fit with prevailing beliefs about human origins. Such a modern looking skull, as the original reconstruction of KNM-ER 1470 came out, was being dated at an older age than many other much older looking australopithecines. This just ran at odds with the prevailing paradigm. So, interestingly enough, KNM-ER 1470 began to evolve! In the period between 1977 and 1995 various reconstructions started to emphasize the ape-like characteristics of KNM-ER 1470 more and more and de-emphasize the human characteristics. If you really want to see subjective manipulation at work, consider the following illustrated evolution of the profile of KNM-ER 1470 over the years. 61

Notice how the reconstruction of this fossil skull evolved based on subjective interpretations of where this fossil should fit in the evolutionary tree. Also note that Richard Leakey himself revised his original reconstruction by 1995. As it turns out, the 1992 reconstruction by Tim Bromage, an expert in hominid bone development, is probably the most objective reconstruction of all. Before beginning his study of 1470, Bromage expected to find that 1470 was probably going to be similar to Dart's famous "Taung child". But to his surprise, he found that the deposition and resorption patterns of bone growth of the 1470 skull were typical of monkeys and apes. Bromage explained that when 1470 was first reconstructed that its face was fitted to the cranium almost vertically - giving it a more human-like appearance. Yet, Bromage's studies demonstrated that the face really jutted out considerably, much like australopithecines. 61,63 In the 1992 issue of New Scientist, Bromage noted the following about KNM-ER 1470:

"When it [KNM-ER 1470] was first reconstructed, the face was fitted to the cranium in an almost vertical position, much like the flat faces of modern humans. But recent studies of anatomical relationships show that in life the face must have jutted out considerably, creating an ape-like aspect, rather like the faces of Australopithecus." 63

Of course, Bromage does not totally reject Skull 1470 as possibly belonging to the genus Homo, but this opinion seems to be mostly based on the larger size of the skull in comparison with other australopithecines. Yet, it is also possible that the latest estimates of 752 cm 3 may still be too large for Skull 1470 - given the view of its more enhanced "ape-like" skull morphology and its long forward-jutting jaws and non-existent forehead. Considering the subjective nature of interpreting this skull and its changing reconstructions over time, it seems less than solid to hold it up as any sort of definite "missing link" between apes and humans - especially given the rather marked similarities of KNM-ER 1470 with the Turkana Boy skull, which was found in the very same region (see below)

In any case, it is interesting to see how scientists interpreted and reinterpreted this skull over the past 30 years. For example, Professor A. Cave, who first suggested that Neanderthal Man was completely human, examined 1470 in London and concluded, "As far as I can see, typically human." In addition, Leakey found two complete femurs, a part of a third femur, and parts of a tibia and fibula near the skull, which he said, "cannot be readily distinguished from Homo sapiens." 10 However, as previously discussed, the problem for 1470 being interpreted as completely human, even at with its original construction, was its relatively small brain size of only 750cc - which is too small for humans and yet very large for an ape. Modern humans average about 1350cc. Some scientists suggested early on that 1470 might have been a human child. But, it was argued that although the cranium was small, that the face is relatively large and developed and therefore unlikely that of a child. Some others argued that it may have been a pygmy human since the lowest known cranial capacity for a non-pathologic human is 790cc 7 and that p ygmies also have other similar facial features such as jutting teeth and face and a relatively small chin. 18

Then, of course, the biggest problem was the fact that 1470 did not fit the dating scheme of the day. The skull itself was found under a layer of volcanic ash. Since volcanic material can be dated using potassium-argon and other radiometric dating techniques, it was reasonably thought that the skull itself should be as old or older than this ash. Richard Leakey had assumed an age of approximately 2.9 million years (Ma) for KNM-ER 1470. If supported by radiometric analysis, this age would make him the discover of the oldest hominid fossil found up to that time. Certainly this would be quite a feather in his cap. However, in 1969 (a few years before KNM-ER 1470 was actually found in 1972) samples of ash from the overlying KBS tuff had been sent sent to Cambridge University for potassium-argon dating. Three different tests returned an age of about 220 Ma, (Fitch & Miller 1970, Nature 226:226-8) 13,62 which would certainly make this hominid discovery very old indeed! Of course, this was impossible and thus obviously wrong given the presence of Australopithecine hominids and other mammalian fossils beneath the tuff . So, these errors were blamed on inappropriate sampling or extraneous argon age discrepancy. It was also noted that the dating of the tuff was complicated because the tuff was a water-transported mixture.

Eventually, however, the tuff was "securely dated" to around 2.6 million years by other "independent methods" to include the following:

  • Vertebrate faunas -- Elephant, Suid (pig), Australopithecus, and tools (Maglio, 1972 Nature 239:379-85, Leaky, 1967-69, etc.)

  • Potassium-Argon dating -- selected crystals (K-Ar and Ar40-Ar39) (Fitch & Miller '70, Nature 226:226-8 and see 251:214)

  • Paleomagnetism -- polarity data, based on 247 samples below KBS tuff (Brock & Isaac, 1974, Nature 247:344-48)

  • Fission Track Dating -- involving uranium, noting possible reanealing (Hurford, 1974, Nature 249:236 '76, 263:738)

Other anthropologists, notably Johanson's team at Berkeley, couldn't accept any claim of such modern hominids in strata dated almost 3 million years old. They tried to re-date the KBS tuff. It was a complex problem because the tuff is a slurry of volcanic debris. But they did find and publish a date that was suitable to them: 1.8 million years, based on:

  • Hominid Fossils -- Skull 1470 and other similar skulls below KBS tuff

  • Potassium-Argon (K-Ar) -- on pumice from the KBS tuff and Ar-Ar -- on selected feldspar crystals (Ar40-Ar39) (Curtis et al,1975, Nature 258:395 (& see 284:229,230 & 294:123)

Then in the late 1970's, a remarkable thing happened. One by one (with much heated controversy apparent in the papers) the other "independent methods" re-evaluated their work in light of the new radiometric date, and confirmed the new age:

  • Paleomagnetism -- pinpointing a different polarity reversal, in light of the change in the K-Ar date (Hillhouse et al, 1977, Nature 265:411)

  • Vertebrate Faunas -- three suid (pig) species (based on teeth) suggesting possible phylogenetic branching and its timing in relationship to the new radiometric date (Cooke, 1978 Science 201:460-63 (&198:13-21)

  • Fission Track Dating -- (U-238 in zircon) emphasizing re-annealing, in light of the change in the accepted K-Ar date (Gleadow, 1980, Nature 284:229-230)

By 1980 there was a new "remarkably concordant" well-accepted radiometric date.

Many more dates than those mentioned here were obtained by radiometric methods, but the choice of which one to accept was made on the basis of the fossils, because the acceptable range of dates for each fossil form was known (by evolutionary theory). At each change, the authors may well have sincerely felt that they were separating truth from error, but how did they know whether a newly calculated date (1.8 or 2.6 or 200 million) was right or wrong? - outside of knowing, ahead of time, the general range of dates that would be at least 'reasonable'?

You see, if the deposit had Australopithecines in it, it obviously could not be 200 million years old, but 2.6 million was close enough to what was expected to be considered "correct". However, when it was found that the layer contained even more modern looking hominid skulls, even the 2.6 Ma estimate could not be correct either. That is why this date was subsequently revised to 1.8 Ma.

So, it was the fossils that gave the constraints for the dates -- or, rather, the accepted evolutionary age of the fossils was the criterion that gave the constraints for the acceptable geologic age of the strata. When the known fossil data changed (along with their corresponding acceptable ages), the acceptable age for the age of the geologic strata also changed accordingly.

This is a clear case where the assumed ages of the fossils (ages based on evolutionary assumptions) strongly influence the accepted ages of the geologic strata that contain the fossils. Doesn't this seem just a little bit circular?

Is this an isolated case? Not at all. In studies where a range of dates is obtained, the ones in the right ball park are presented, giving the limits of what is assumed to be the correct age, and the anomalous ones (if mentioned at all) are explained in terms of mixing of sediments, extra Argon retention, leaching, and other very plausible processes. The explanations for anomalously old or anomalously young ages may be quite accurate. On the other hand, these arguments may just as reasonably apply to the accepted ages as well. If no acceptable age is found, the results may not be published at all.

My point is that the accepted ("non-anomalous") age is the age within the timeframe set by evolutionary theory. So it is evolutionary theory that dictates which radiometric and other dating results will be acceptable to publish as the age for a fossil.

To go into a bit more detail, consider further the argument that the KBS Tuff is an example of the redepositio n of volcanic ash. Therefore, the old dates returned by the Cambridge laboratory on three different occasions were thought to be the result of analysis of old sediment that had been mixed in with the new and deposited atop the relatively young fragments of KNM-ER 1470. Because of this argument, it was recommended that new samples be collected from which suitable individual crystals could be separated. These new samples were dated at 2.61 +/- 0.26 Ma, based on the 40 Ar/ 39 Ar ("Argon-Argon") dating method (thought to be more accurate than the origina lPotassium - Argon d ating technique). 13 However, over the following decade, the rocks surrounding 1470 were dated many times using various methods - to include the 40 Ar/ 39 Ar method . The different tests gave widely varying results. For example, two specimens from the same layer were analyzed by the same people (Fitch and Miller) using the same technique during the same analysis. One specimen was dated at 0.52 to 2.64 Ma. The other was dated at 8.43 to 17.5 Ma. 24, 62 Fitch and Miller attributed the spread to reheating of the crystals after deposition (reheating is no longer thought to have occurred). Paleomagnetic studies also gave ambiguous results. Many many tests were done, and the "best" or "most acceptable date" was placed at about 2.61 Ma. 13, 62, 72

This, of course, did not impress Richard Leakey. I n June of 1973, in an interview with National Geographic, he said,

"Either we toss out the 1470 skull or we toss out all our theories of early man. It simply fits no previous models of human beginnings. 1470 leaves in ruin the notion that all early fossils can be arranged in an orderly sequence of evolutionary changes."

What was the problem? The problem, given the age of 2.61 Ma, made 1470 contemporaneous with Australopithecus, if not older, and yet 1470 was assembled by Leakey's wife to looked quite similar to modern man. Given such a reconstruction, this human-like appearance absolutely unseated Australopithecus as an ancestor of modern man.

In later lectures, Richard Leakey rarely made reference to 1470. However, in a PBS documentary in 1990 he stated,

"If pressed about man's ancestry, I would have to unequivocally say that all we have is a huge question mark. To date, there has been nothing found to truthfully purport as a transitional specie to man, including Lucy, since 1470 was as old and probably older. If further pressed, I would have to state that there is more evidence to suggest an abrupt arrival of man rather than a gradual process of evolving." 10

Now that is a very startling statement coming from a man who has devoted his whole life to finding the evolutionary remnants along the pathway towards modern humans.

The human-like appearance of 1470 coupled with its age of 2.6 Ma was also a very big problem for Johanson who considered his A. afarensis (Lucy) to be an important evolutionary link between apes and man. With a more human appearing 1470 around that was either a contemporary of A. afarensis, or even slightly older (an age range for Lucy of 2.5 to 3.7 Ma), his fossil was unlikely to be directly ancestral to man. So, Johanson wished to have 1470 "re-dated" - obviously! Why didn't anyone else think of it?

Lucy herself had been dated by several radiometric methods whose published results varied from 2.5 to 3.7 Ma. The age of 2.9 Ma had been chosen as the most probable age. So, Johanson asked for the help of Basil Cooke, who had assembled a detailed two million year sequence of fossil pig lineages which he says was consistent over a wide geographical area. This data was based on what was assumed to be a constant but rapid rate of evolution in length of the third molar of certain pig fossils found in southern Ethiopia. These "index pigs" were used to re-date Leakey's 1470 at less than 2 Ma (

1.8 Ma), which placed it on the desired human side of Lucy. Then, Johanson decided to date Lucy again in an effort to see if he could make her a little older. In his book "Lucy, The Beginnings of Human Kind" Johanson said, "That meant turning to Basil Cooke and his pig sequences. These had already straightened out a dating puzzle at Lake Turkana and shoved Richard Leakey's 1470 H. habilis skull forward from 2.6 Ma to less than 2.0 Ma. Perhaps they could do it for Lucy too. But, in this case, they would be stretching her age not shrinking." Needless to say, Cooke came through as expected and said that his pig sequence showed that, "an age of 3.0 - 3.4 Ma would give a better fit than the previous 2.9 Ma age for Lucy." 10

To make matters even more confusing, Garnis Curtis, at Berkeley, has used potassium-argon dating on the KBS tuff and came up with younger dates yet. His first series of tests showed it to be 1.8 myo and his second series of tests showed it to be 1.6 Ma. Note that initial fission track studies of zircons from the KBS tuff indicated an age of 2.44 +/- 0.08 Ma (Hurford et al. 1976). Compare this with subsequent fission track studies of zircons in the same tuff returning dates of 1.87 +/- 0.04 Ma (Gleadow 1980). Another expert, Ian McDougall, was also called in to do independent dating. Knowing about the controversy and what the desired date should be ahead of time, it is not at all surprising that McDougall came up with an age of 1.89 +/- 0.01 Ma using K-Ar dating and 1.88 +/- 0.02 Ma using 40 Ar/ 39 Ar dating (McDougall et al. 1980 McDougall 1981, 1985). 72 It just doesn't seem like blinded studies are very popular when it comes to geochronology. It's almost like geologists and anthropologists have never heard of blinded studies.

Dalrymple and Lanphere sum up what might be considered just a bit circular in the following statement:

"If the potassium-argon ages of a group of rocks agree with the stratigraphic sequence, determined on the basis of physical relationships of fossil evidence, then the probability is good that radiometric ages are reliable. " 14

Ancient Bones with Modern Bones?

Now, we must not forget about the human-like femur that was associated with KNM-ER 1470, even though located several kilometers away from the skull fragments. Although this femur and leg bones "did not differ from those of modern humans in any feature related to movement or posture", they were associated with 1470 simply because they were found in the same layer. 66,67 Obviously it is impossible to have modern humans living with H. habilis creatures since modern humans had not evolved yet - right? And yet we know now, through the discovery of more reliable indicators of general posture, that many creatures designated as H. habilis, to include KNM-ER 1470, were not even close to the modern-human bipedal posture. So, what is a modern-human-looking femur and leg bone fragments doing in the same layer as a creature that we know did not habitually walk in an upright manner?

Remember the work of Dr. Spoor on the inner ear labyrinths of H. habilis specimens and his conclusion (based on the angle of these labyrinths as compared with modern humans, H. erectus, Australopithecus, and many other hominids) that H. habilis "relied less on bipedal behavior than the australopithecines"? Other specimens, such as SK 847, have been grossly misclassified, based on weaker morphologic evidence, as somewhere between H. erectus and H. habilis when there is an "extreme difference" between the "modern-human-like labyrinth of SK 847 and the australopithecine labyrinth of Stw 53" (i.e., H. habilis). 65 I wonder what the inner ear canals of KNM-ER 1470 would look like?

How bad do such morphologic interpretations have to get before we start to suspect that the storytelling of anthropologists about the supposed evolution of humans from ape-like creatures is not worth the paper that it is written down on? Isn't it all starting to sound like a lot of fanciful storytelling?

Obviously this whole issue of the placement of KNM-ER 1470 in the evolutionary sequence of hominids has turned out to be quite a subjective mess for anthropologists. In fact recently Bernard Wood and Mark Collard published some rather revealing if not humorous conclusions in the April, 1999 issue of Science where they actually suggest that the "Homo" genus is "not a good genus" as it currently stands and that some of the oldest and most significant fossils assigned to Homo, to include bothH. habilis and H. rudolfensis, should be "transferred to the genus Australopithecus" :

"More recently, fossil species have been assigned to Homo on the basis of absolute brain size, inferences about language ability and hand function, and retrodictions about their ability to fashion stone tools. With only a few exceptions, the definition and use of the genus within human evolution, and the demarcation of Homo, have been treated as if they are unproblematic. But . recent data, fresh interpretations of the existing evidence, and the limitations of the paleoanthropological record invalidate existing criteria for attributing taxa to Homo. in practice fossil hominin species are assigned to Homo on the basis of one or more out of four criteria. . It is now evident, however, that none of these criteria is satisfactory. The Cerebral Rubicon is problematic because absolute cranial capacity is of questionable biological significance. Likewise, there is compelling evidence that language function cannot be reliably inferred from the gross appearance of the brain, and that the language-related parts of the brain are not as well localized as earlier studies had implied.

In other words, with the hypodigms of H. habilis and H. rudolfensis assigned to it, the genus Homo is not a good genus. Thus, H. habilis and H. rudolfensis (or Homo habilis sensu lato for those who do not subscribe to the taxonomic subdivision of "early Homo") should be removed from Homo. The obvious taxonomic alternative, which is to transfer one or both of the taxa to one of the existing early hominin genera, is not without problems, but we recommend that, for the time being, both H. habilis and H. rudolfensis should be transferred to the genus Australopithecus." 64

Even more recently, as of August 2007, the journal Nature published the latest discoveries of Meave Leakey and her team, to include Frederick Kyalo Manthi. In short, they found the complete skull of Homo erectus within walking distance of an upper jaw of Homo habilis (in 2000), with both dating from the same general time period. According to their own report, they concluded that this finding makes it "unlikely that Homo erectus evolved from Homo habilis." 74

Co-author Fred Spoor, professor of evolutionary anatomy at the University College in London commented:

"The two species lived near each other, but probably didn't interact, each having its own "ecological niche," Homo habilis was likely more vegetarian while Homo erectus ate some meat, he said. Like chimps and apes, "they'd just avoid each other, they don't feel comfortable in each other's company. There remains some still-undiscovered common ancestor that probably lived 2 million to 3 million years ago, a time that has not left much fossil record. Overall what it paints for human evolution is a chaotic kind of looking evolutionary tree rather than this heroic march that you see with the cartoons of an early ancestor evolving into some intermediate and eventually unto us." 74

Bill Kimbel, science director of the Institute of Human Origins at Arizona State University, notes:

"The more we know, the more complex the story gets. Scientists used to think Homo sapiens evolved from Neanderthals, he said. But now we know that both species lived during the same time period and that we did not come from Neanderthals. Now a similar discovery applies further back in time." 74

Another co-author, Susan Anton, a New York University anthropologist, she expects anti-evolution proponents to seize on the new research, but said it would be a mistake to try to use the new work to show flaws in evolution theory.

"This is not questioning the idea at all of evolution it is refining some of the specific points," Anton said. "This is a great example of what science does and religion doesn't do. It's a continuous self-testing process." 74

And there you have it. The Theory of Evolution is a self-testing process as long as it never crosses one's mind to question or subject the basic theory itself to testing and potential falsification. Despite their claims to the contrary, evolutionary scientists, like people in general, are quite biased, even dogmatic and religiously fundamental, in their thinking. Question and challenge anything and everything except the one holy untouchable doctrine - The Doctrine of Darwinian-style Evolution itself. If the puzzle pieces don't fit, change, warp, and twist the theory until they do. It doesn't seem to matter what kind of evidence presents itself, evolutionists have an uncanny ability to continually modify their theory to meet the new data.

The Theory of Evolution is a truly wonderful theory - a theory that is so fluid that it can explain any and all data, not matter how contrary to previous notions of reality. Oh no, creationists and intelligent design theorists have nothing on evolutionists when it comes to subjective manipulation of a pet theory to fit whatever comes along.

Turkana Boy -- In July 1984, a nearly complete fossilized skeleton, of an obviously human 12-year-old boy (some say as young as 9 years old), was discovered at Lake Turkana in Kenya. It is the most complete skeleton to date to be included as a Homo erectus. The boy stood 160cm (5' 3'') tall and had a brain capacity of 880cc. It is estimated that in adulthood, the boy would grow to be 185cm (6' 1'') tall and have a brain capacity of 910cc. The skeleton of this child is like that of a modern human in all respects except for certain details of the skull. He had a low forehead and pronounced brow ridges. Richard Leaky said, "This boy would go unnoticed in a crowd today." Since this human skeleton was found in strata dated at 1.6 Ma, this supposed age, combined with some fairly minor skull details, makes it another representative of the taxon Homo erectus. 10

But, there's just one more interesting thought to consider. Remember that another famous skull was found in this Lake Turkana region. That's right KNM-ER 1470 was found in this same region. Notice the striking similarities when the reconstruction of KNM-ER 1470 is put side-to-side with the Turkana Boy skull (see below). Now isn't that just most interesting? - or is it just me?

: Peking Man: The current story is that the remains of Sinanthropus pekinensis, known as Peking Man and dating back to 400,000 BC, were excavated in 1923 at Zhoukoudianzhen near Peking, China. Peking Man was closely related to Pithecanthropus of Java and "lived during the Old Stone Age."

An almost complete skullcap was discovered in 1929 in a filled-in limestone cave near Peking, China (now Beijing). This ape-like skullcap was similar to Java man. The cave continued to be investigated until the beginning of World War II. (All original fossil remains have since been lost in transport to America to "save them" from the Japanese invasion of WWII. However, some relatively good casts of portions of skulls remain.) Fragments of 14 skulls, 12 lower jaws and 147 teeth were found. Also, several skeletons of "Homo erectus" were found slightly higher (Not called Homo sapien only because of their assumed ages of > 1my even though very similar to modern man). Once again, bone fragments were assembled from various places to form a skull where the jawbone came from a level 85 feet higher than the skullcap and face bones. After hiring a sculptor to model a woman's face from the made-up skull, the result was named "Nellie." The very "attractive" Nellie has appeared in almost all modern textbooks concerning the evolution of man. 10

The most complete fossils found in the cave, all of which were braincases or skullcaps, are:

Skull III, discovered at Locus E in 1929 is an adolescent or juvenile with a brain size of 915 cc.

Skull II, discovered at Locus D in 1929 but only recognized in 1930, is an adult or adolescent with a brain size of 1030 cc.

Skulls X, XI and XII (sometimes called LI, LII and LIII) were discovered at Locus L in 1936. They are thought to belong to an adult man, an adult woman and a young adult, with brain sizes of 1225 cc, 1015 cc and 1030 cc respectively. (Weidenreich 1937)

Skull V: two cranial fragments were discovered in 1966, which fit with (casts of) two other fragments found in 1934 and 1936 to form much of a skullcap with a brain size of 1140 cc. These pieces were found at a higher level, and appear to be more modern than the other skullcaps. They were given a different name of "Upper Cave Man". (Jia and Huang 1990)

At the site where "she" was found there were also numerous stone tools and evidence of butchery and fires. Recently, Chinese scientists have found over 1,000 stone tools, the skulls of over 100 modern day animals, and 6 modern human skulls (Upper Cave Man). The skulls and many fragments showed evidence of being at least possibly shattered or broken-in at the occipital area. Perhaps humans were butchering and eating apes? Perhaps, but some argue that this area is the weakest area of the skull. Therefore, the finding of shattered occipital regions it is not proof of butchery.

In addition, a layer of ashes nearly three meters thick was found. Even so, little consideration seems to be given to the possible creation of fires and tools by actual Homo sapiens. 10 Once again, it is felt that since most of the skulls seem to have been very large, and similar to Java Man and other Homo Erectus fossils, that these must be intermediates to humans? despite the many similarities to apes, which, according to Boule and Vallois, include three jaw characteristics of apes and one of human and three teeth characteristics of apes and one of human. 22 Again, knowing that many modern animals have gigantic counterparts in the fossil record, this might be like saying that a Great Dane is an intermediate between a Chihuahua and a horse. There might be more anatomic similarities including larger head and cranium and even shape of head? but what does this prove? Do the similarities in anatomy prove this theory of dog-horse evolution and negate the differences in anatomy? Beginning with the idea that modern apes start out with a great deal of similarities to modern humans, establishing an evolutionary connection without living specimens and on fragmentary fossil evidence, involves at best, more than its fair share of guesswork and just-so story telling. In fact, this sort of story telling sounds very similar to the stories of the "First Frenchmen" that were invented to explain the various remains and artifacts found in different layers at Font 飨 evade Cave (see story below). (Back to Top)

Java Man (Pithecanthropus erectus) - According to current evolutionary th eory, the earliest specimens of H. erectus, found in 1891-92 near Trinil on the Indonesian island of Java (thus called Java man), are "about 700,000 years old." The teeth of Java man, found separately and which are now thought to belong to an orangutan, were said to be remarkably like those of H. habilis of eastern Africa, suggesting that "H. erectus might have evolved from H. habilis. " (Compton's Encyclopedia)

The actual story begins shortly after Darwin published his "On the Origin of the Species." A Dutch physician named Eugene Dubois, who greatly desired to find the "missing link" between apes and man, went in search of Haechel's "Pithecanthropus" in Sumatra. (Dubois had been a student of Ernst Haeckel who is famous for his "Biogenetic Law," which stated that the human embryo went through the sequential evolutionary stages of its ancestors. It is now well known that this is far from true. What else is well known is that Haeckel falsified much of his data.) 1 5

Having failed to get financial assistance from the Dutch government, Dubois enlisted as a surgeon in the Royal Dutch Army in order to be stationed in Sumatra. While in Sumatra, he heard about a skull found on the nearby island of Java. He was able to secure the skull and even found another like it at the same location. However, these skulls were too human looking to be of any use to someone looking for an ape-man. In 1891, he found a molar tooth along the Solo River. Later the same year, he found another molar and an ape-like skullcap. The following year he found a human femur some yards from where he found the skullcap. Although at first he thought it was a chimpanzee skull, after consulting with Haeckel, he declared the whole collection to belong to one and the same creature, stating that it was "admirably suited to the role of missing link." 10

This missing link arrived just in time to salvage Darwin's theory, as it was under fire because of the total lack of transitional fossil evidence. By joining an ape skull with a human femur he had truly created an ape-man. He originally claimed that the stratum he was working in was Pliocene but after discovering his ape-man, he decided it was really tertiary. 10 When taking his specimen on tour, respected scientists, such as the great anatomist Rudolph Virchow, refused to chair any of his meetings. Nonetheless, newspapers and magazines embraced him wholeheartedly, including many pictures of Dubois's ape-men.

Through association of a human-like femur with a very large gibbon-like skullcap, Dubois created "Java Man." The leg bone was almost certainly that of a modern human. The skullcap is still hotly debated as that of an extinct gibbon-like creature or of a human ancestor. One important fact is that the association of the femur (found a year later and twelve meters away) and skullcap is not scientifically justified. It was in recognition of this fact that the restoration of Java Man, paid for by Ernst Haeckel, was removed from the Leiden Museum to its basement and in the mid 1980s. The exhibit of Java Man was also removed from public display in the American Museum of Natural History. 7 Dr Rudolph Virchow, Director of the Berlin Society for Anthropology and founder of the science of pathology, examined Dubois' fossils and wrote, "The skull has a deep suture between the low vault and the upper edge of the orbits. Such a suture is found only in apes, not in man. Thus the skull must belong to an ape. In my opinion this creature was an animal, a giant gibbon in fact. The thigh bone has not the slightest connection with the skull." 8,20

Eugene Dubois himself appears to have never given up the idea that his "giant gibbon" was an intermediate between the gibbon and man. Some today continue to hold onto Java Man as an intermediate. It is argued that Java Man had an intermediate brain size much larger than that of a modern gibbon (940cc vs. 100cc) and yet smaller than that of an average modern man (1350cc). It is also said that Java Man obviously walked upright and is therefore an intermediate. How is it so clear that Java Man walked upright (bipedal) when all there is, is a skull cap? Well, it is said that the skullcap is very similar to the skullcap of another "Homo Erectus" skeleton (WT15000) among several others. Since it is generally agreed that WT15000 walked upright, then obviously Java Man walked upright too. Despite the fact that there exists, in the fossil record, evidences of huge animals with much larger heads and brains than their modern day counterparts, it is still suggested that such a large gibbon could not possibly have been - Just a gibbon. (Back to Top)

Neandertal (orNeanderthal) Man (Homo neanderthalensis): This was the first "ape-man" found in Darwin's day. Of the cases stated above, most tried to make men out of apes. Now we will see how to make apes out of men.

In 1856, in the Neander Valley of Germany, a schoolteacher, Johann Fuhlrott, found a skeleton that consisted of a skullcap, thighbones, part of a pelvis, some ribs, and some arm and shoulder bones in a small cave at Feldhofer. The lower left arm had been broken in life, and as a result the bones of the left arm were smaller than those of the right. A careful examination and description by Professor Schaafhausen reported them to be human and normal. Two years later, two similar skulls were found in Belgium. Subsequently, over 60 parts of skeletons were found in eleven different countries. (They are still being found today). 10

In 1908, Professor Boule of The Institute of Human Paleontology in Paris declared Neanderthal an ape-man because of his low eyebrow ridges and the stooped over posture of some of the specimens. This was to shape opinion and teaching for most of the 20th century. However, in 1950, things began to change. An embarrassing fact came out. Neanderthal man's average brain capacity was larger than modern man's by over 200 cc's. Some also claim that Neanderthal man, at least the stooped over ones, suffered from acute osteoarthritis. 10

Many Neanderthal skeletons have been found now, and not just a few here and there. In 1872 Dr. Rudolph Virchow, the father of pathology, claimed that these skeletons were nothing more than modern man with rickets and arthritis. In 1957 anatomists Straus and Cave released a comprehensive study of Neanderthal and concluded that the toes were not prehensile, the pelvic structure was not at all ape-like, and the bones all showed strong evidence of severe arthritis. In 1970, medical specialist, Ivanhoe, showed a vitamin-D deficiency in all Neanderthal samples. This he surmised was the cause of the severe arthritis. Dr. C. Coring Brace stated that, "West European Neanderthal Man is simply today's West Europeans." The Chicago Field Museum has since put in a newer exhibition of Neanderthal man looking more fully human. 10

Modern science has finally come up with a ready answer for their problems with Neanderthal man. He was an "evolutionary dead-end." 10

There are many scientists who say that Neandertal Man did not actually have rickets, and that pathology was not responsible for their most unique characteristics such as brow ridges, low vaulted craniums, and very strong stocky builds which separate them from any known ethnic group living today. Here is a list of the most distinct characteristics:

The skull is lower, broader, and elongated in contrast to the higher doming of a modern skull.

The average brain size (cranial capacity) is larger than the average modern human by almost 200 cubic centimetres.

The forehead is low, with heavy brow ridges curving over each eye.

There is a slight projection at the rear of the skull (occipital bun).

The cranial wall is thick compared to modern humans.

The facial architecture is heavy, with the mid-face and the upper jaw projecting forward (prognathism).

The nose is prominent and broad.

The frontal sinuses are expanded.

The lower jaw is large and lacks a definite chin.

The body bones are heavy and thick and the long bones somewhat curved.

Judging from the very wide varieties of ethnic groups living today, especially the more inbred ones, such characteristics are not too difficult to explain by simple ethnicity which has since been lost or bred out in modern Europeans. Many modern cultures have had extreme anatomical features. With subsequent cultural intermixing, such distinguishing features have often been lost. So, unique anatomical features do not necessitate Neanderthal Man as being separate from Homo Sapiens. In fact, Thomas Huxley himself seemed to recognize this problem. Donald Johanson wrote something very interesting about what Huxley did in setting up a sequence of modern skulls to link Neanderthals to modern humans.

"From a collection of modern human skulls Huxley was able to select a series with features leading 'by insensible gradations' from an average modern specimen to the Neandertal skull. In other words, it wasn't qualitatively different from present-day Homo Sapiens." 26

This series of skulls could easily be set up today. Obviously therefore, there is no clear or consistent morphologic difference between Neanderthals and ourselves. Any variation can be selected out and categorized according to arbitrary rules, but such categories do not necessitate evolutionary relationships any more than ethnic variations that exist today suggest such relationships.

Then there is the argument of Neanderthal DNA. On July 11, 1997, the announcement was made in the journal Cell that Neanderthal mitochondrial DNA (mtDNA) had been successfully recovered and sequenced by Svante Pääbo and his team. 25 Of course there were statistical differences between Neanderthal DNA and the DNA of modern humans. These differences were used to calculate the evolutionary divergence of Neanderthals from a common ancestor to around 550,000 to 690,000 years ago. It is thought that Neanderthals then became extinct without contributing mtDNA to the modern human genome. In other words, Neanderthals were just one of many offshoots or splinter groups that became extinct but who were not direct links to modern humans in our evolutionary branch.

However, there are just a few problems with this theory. One problem has come to the forefront with movies such as Jurassic Park and with the publicity of the O.J. Simpson murder trial where DNA technology played a prominent role. Some problems that were brought more clearly to light by these media events is that DNA does not last very long. It breaks down fairly rapidly depending on environmental factors. Even under the most favorable conditions, many scientists believe that DNA cannot remain identifiably intact beyond a few tens of thousands of years. 27,28 In light of this fact, it is unlikely that very many Neanderthal skeletons would contain intact DNA, even with such relatively "young" remains dating to between 30,000 and 50,000 years. The common explained solution to this problem is that in certain environments, especially very dry and cold environments, DNA can last much longer than it can in warm wet environments. However, even in these "protective" environments, DNA still breaks down at a fairly rapid rate. The rate is so rapid in fact that few scientists believe that it could last much beyond 50,000 years. Because of these decay problems, the reports of DNA being recovered from insects trapped in amber that is millions of years old are now being called into serious question. 29 In any case, even for Neanderthal bones that are thought to be fairly "young", finding DNA that can still be sequenced is turning out to be quite a rare find indeed. Because of this problem, repeatability is becoming a real issue in the study of Neanderthal DNA. As it turns out, mtDNA recovery from Neanderthals has only been done three times. Others have found it very difficult to repeat Svante Pääbo results. Since the scientific method is based on repeatability, the whole issue of Neanderthal mtDNA and its implications comes into question. Consider the following comment from Svante Pääbo himself:

"Preserved Neandertal DNA is likely to be rare, and the DNA in the type specimen [the 1856 Neander Valley Neandertal fossil] may result from its unique preservation conditions. Most Neandertal specimens are therefore unlikely to contain amplifiable DNA." 30

Despite these problems, Pääbo et al. seemed to have finally overcome them in 1997 when they sequenced the very first mtDNA isolated from a Neanderthal skeleton (Note: The fact that a given cell has many more copies of mitochondrial DNA than the single copy of nuclear DNA (nucDNA) is suggested as a reason why mtDNA might be a bit easier to isolate than nucDNA). Pääbo and his team presented their findings as follows:

"The Neandertal sequence was compared to 994 contemporary human mitochondrial lineages, i.e., distinct sequences occurring in one or more individuals, found in 478 Africans, 510 Europeans, 494 Asians, 167 Native Americans and 20 individuals from Australia and Oceania. Whereas these modern human sequences differ among themselves by an average of 8.0 (range 1-24) substitutions, the difference between the humans and the Neandertal sequence is 27.2 (range 22-36) substitutions. Thus, the largest difference observed between any two human sequences was two substitutions larger than the smallest difference between a human and the Neandertal." 25

The conclusions drawn were as follows:

"When the comparison was extended to 16 common chimpanzee lineages, the number of positions in common among the human and chimpanzee sequences was reduced to 333. This reduced the number of human lineages to 986. The average number of differences among humans is 8.0 (range 1-24), that between humans and the Neandertal, 25.6 (range 20-34), and that between humans and chimpanzees, 55.0 (range 46-67). Thus, the average number of mtDNA sequence differences between modern humans and the Neandertal is about three times that among humans, but about half of that between modern humans and modern chimpanzees.

To estimate the time when the most recent ancestral sequence common to the Neandertal and modern human mtDNA sequences existed, we used an estimated divergence date between humans and chimpanzees of 4-5 million years ago and corrected the observed sequence differences for multiple substitutions at the same nucleotide site. This yielded a date of 550,000 to 690,000 years before present for the divergence of the Neandertal mtDNA and contemporary human mtDNAs. When the age of the modern human mtDNA ancestor is estimated using the same procedure, a date of 120,000 to 150,000 years is obtained, in agreement with previous estimates. Although these dates rely on the calibration point of the chimpanzee-human divergence and have errors of unknown magnitude associated with them, they indicate that the age of the common ancestor of the Neandertal sequence and modern human sequences is about four times greater than that of the common ancestor of modern human mtDNAs.

The Neandertal mtDNA sequence thus supports a scenario in which modern humans arose recently in Africa as a distinct species and replaced Neandertals with little or no interbreeding." 25

If mtDNA was in fact isolated from the Neanderthal bones, these conclusions might seem reasonable until one considers a few more facts. The Cellarticle itself noted that the range of sequence differences for modern human mtDNA goes from 1 to 24 with an average of 8 substitutions. The mtDNA sequence differences between modern humans and the single Neanderthal fossil range from 22 to 36 substitutions, with the average being 27. In other words, the two most different humans analyzed in this study, as far as mtDNA substitutions are concerned, are different by 24 substitutions. The closest that any human in this study was to the single specimen of Neanderthal mtDNA was 22 substitutions. This means that there are some people living today that are closer to Neanderthals in their mtDNA sequencing than they are to some other modern human beings. Someone might be found to be only 22 substitutions away from our Neanderthal, but 24 substitutions away from his own next-door neighbor. Interesting isn't it? If Neanderthals are classed as separate species because of these differences, which one of our modern human volunteers should be classify as a separate species? Perhaps the one who was only 22 substitutions different from the Neanderthal? Or, maybe his next-door neighbor who is 24 substitutions away from his neighbor as well as 22 substitutions away from our Neanderthal friend? I mean, some of us might have neighbors that look like Neanderthals (or maybe we might look like Neanderthals compared to our neighbors), but can a different species really be assumed based on a difference of 20-some substitutions in a particular hypervariable region of DNA?

"The computation of pairwise distances between the 171 randomly selected sequences and the Neandertals rendered 1.6% of human-human comparisons larger than the smallest difference between Neandertals and humans. Likewise, 27% of the comparisons are lower than the largest human-human difference. This result suggests that Neandertals sequences are not so different from those of extant humans, in contrast to the NSG claims." 50

For additional information regarding this issue, see a debate between myself and John Harshman from ( Link ).

There have been attempts by popular scientists to describe exactly how this mtDNA evidence turns Neanderthals into separate species. Some describe it as a group of early Homo sapiens huddled around a fire. Some are shoulder to shoulder while others, on the other side of the fire might be several feet away. maybe even 24 feet away. However, the average distance that any one person is from any other person is just 8 feet. Now we notice a dark Neanderthal figure in the shadows far from the fire. He averages 27 feet away from any given Homo sapien huddled around the fire. Obviously therefore, he is an outsider, a different species all together.

However closer inspection reveals that some of those huddled around the fire are closer to the Neanderthal than they are to certain others that are also huddled around the fire. Does that make them more closely related to Neanderthals, who belong to a completely different species, than to certain members of their own species? This sounds rather silly does it not? And yet, this is what must be the obvious conclusion. For example, what if we started with the Neanderthal specimen and then picked a person at random out of a crowd. We might get someone who is different by 24 substitutions from our Neanderthal specimen. Now, we pick someone else out of the crowd who just so happens to also be different by 24 substitutions from our Neanderthal specimen and by 24 substitutions from our first human volunteer. Which one is the new species? They are all practically equidistant from each other. In order to visualize the problem, draw three dots on a piece of paper, one for each of our two volunteers and the third dot for our Neanderthal "volunteer." Make sure to draw each one on the paper separated by 24 units of measure from each of the other two dots. Now, pick the one that is the new species and the two that belong to the same species. Maybe there are three separate species represented here? However, all one would have to do to disprove this notion is get two of the volunteers to "produce offspring" so to speak. If that happened, the entire notion that a separation of 20 or so substitutions makes for a new species, would have to be. well. revised somewhat.

Some argue that new and more recent information published by Pääbo and his team in May of 1999, show that my objections to his conclusions are misguided. As it turns out, the range (1-81) for chimp/bonobo substitutions are even wider than previously thought. In other words, if one chose a chimp at random, this chimp might be as many as 81 substitutions different from the chimp swinging on the branches right next to him. This is interesting because this same chimp might be only 78 substitutions different from a given human living at the edge of the forest. This more recent paper also points out that the range between humans (1-35) is also wider than was reported in the first paper. The range between humans and the Neanderthal sequence was also altered in the updated paper to (29-43). 49 Some see this as clear evidence that my arguments are flawed, but personally, I fail to see how. This second paper seems to make it even more clear that substitution differences in a given variable region cannot be used to absolutely measure the boundary between different species. In fact, using this method of reason, it seems like some chimps might be more closely related to certain humans than to certain chimps within their own species. Since this clearly is not the case, this logic seems flawed. Evolutionary conclusions therefore cannot be effectively supported using this these methods.

Why this problem has not been more publicly recognized seems rather strange. I am sure that I am not the first one to wonder about this. And yet, popular scientist seem not even to be aware that there is this problem. It seems that the statistical average of 8 and 27 are so different that this squelches any suggestion that there might be a problem. Using this average difference as a basis for their conclusions, Kahn and Gibbons wrote in the journal Sciencethat these averages put Neanderthal out of the statistical range of modern human variation. 31

This statement is clearly misguided because not only are there humans living today with wider separations between them than our Neanderthal friend, but it is a statistical error or pitfall to compare many different entities with just one entity. In other words, we do not know what the Neanderthal mtDNA average is if there is just one specimen. How then can we know if this one Neanderthal was not a statistical outlier? How do we know that if we but had more Neanderthal samples that the average would not be closer to that of modern humans?

As it turns out, since the first sequence was obtained by Pääbo and his team, there have been two more Neanderthals found who's mtDNA was intact enough to sequence. The second sequence was done in 1999 on a baby discovered in Mesmaiskaya Cave in south-western Russia. This Neanderthal baby is thought to have died 29,000 years ago. The sequence of this baby differed from the first sequence by 12 substitutions. The average number of substitutions between the second Neanderthal mtDNA ("Baby M" for short) and a given human is 22 as compared to 27 from the first Neanderthal sequence. 46,47 In other words, Baby M was "closer to the Homo sapien fire" than the first shadowy Neanderthal. This means that some living humans might be even closer to this second Neanderthal than they are to other living humans by quite a fair margin. Unfortunately however, no figures for the minimum, average, and maximum distances between the second Neanderthal and modern humans was provided.

The third Neanderthal who's mtDNA was successfully sequenced was found in a cave at Vindija, Croatia. In 2000, scientists announced the mtDNA sequencing of this third Neanderthal specimen. This new sequence fell within a 3.75% cluster of the first two sequences. 48 Modern humans cluster at around 3.5%. This is a rather narrow level of diversity when one compares these clusters to chimps (15%) and gorillas (19%). Various human ethnic groups also have rather narrow ranges of diversity in their mtDNA sequencing. Of course, the problem still remains that some humans from certain of these ethic groups are more closely "related" to Neanderthals than they are to certain other living humans from other groups. The question remains as to who should be classed as a separate species?

Maryellen Ruvolo (Harvard University) points out that the genetic variation between the modern human and Neanderthal sequences is within the range of other single species of primates. She goes on to say: " there isn't a yardstick for genetic difference upon which you can define a species." 31

Further confusion comes from the comments in the Cell article that seem to indicate that Neanderthals are more closely related to the ancestral " chimpanzee" than modern humans are. This might not have been the actual intention of the authors, but one could easily get confused by the wording of the article. The fact of the matter is that the single specimen of Neanderthal mtDNA was actually farther away from chimp mtDNA than humans are from chimp mtDNA substitutions. Clearly then, Neanderthal DNA is no closer "related" to chimp DNA than human DNA is. 32

Also, the idea that mtDNA mutations can be used as a molecular clock have been recently called into question by the journal Science. As it turns out, former ideas about the timing of this clock might be in error by as much as "20-fold." The famous "Mitochondrial Eve" once thought to be around 100,000 to 200,000 years old, might now have to be revised to as young as "6,000" years old. 33,34

D. Melnick and G. Hoelzer (Columbia University) tested the assumptions of mtDNA based phylogenic relationships and concluded:

"Our results suggest serious problems with use of mtDNA to estimate 'true' population genetic structure, to date cladogenic events, and in some cases, to construct phylogenies." 35

Jonathan Marks (Yale University) declared mtDNA determined relationships to be highly biased:

"Most analysis of mitochondrial DNA are so equivocal as to render a clear solution impossible, the preferred phylogeny relying critically on the choice of outgroup and clustering technique." 36

In August of 2002, Gabriel Guitierrez et al., from the Universidad de Sevilla, Spain, published a paper in the well known journal, Molecular Biology and Evolution entitled, "A Reanalysis of the Ancient Mitochondrial DNA Sequences Recovered from Neandertal Bones." 50 Consider their conclusions from the following abstract:

"Recent reports analyzing mitochondrial DNA sequences from Neandertal bones have claimed that Neadnertals and modern humans are different species. The phylogenetic analyses carried out in these articles did not take into account the high substitution rate variation among sites observed in the human mitochondrial D-loop region and also lack an estimation of the parameters of the nucleotide substitution model. The separate phylogenic position of Neandertal-Human and Human-Human pairwise distance distributions overlap more than what previous studies suggested. We also show that the most ancient Neandertal HVI region is the most divergent when compared with modern human sequences. However, the opposite would be expected if the sequence had not been modified since the death of the specimen. Such incongruence is discussed in the light of diagenetic modifications in ancient DNA sequences."

In the body of this paper, there were several other statements of interest:

"The NSG [The conclusions of Krings et al., based on their "Neandertal sequencing groups"] reported that the pairwise comparisons between the Neandertal and human sequences demonstrate that Neandertals are outside of modern human D-loop variability. In particular, Krings et al., (1997) stated that 'a total of 0.002% of the pairwise comparisons between human mtDNA sequences were larger than the smallest difference between the Neandertal and the humans.' We think that this point merits further analysis. The current database is biased because of the overrepresentation of some populations and the underrepresentation of others. For instance, the MOUSE database contains 6,012 entries for the HVI region, but 31% of the entries belong to only 20 populations out of 206 populations represented (10% of the total populations). The extreme cases are 306 Koreans, 126 Yaps, 120 Cayapa Amerindians, 119 Mandeka, 115 Palau, and 100 white British. There are also 1,417 entries of undetermined population (40% of them are from North America and 23% European, but only 9% are from Africa). Thus, African populations containing the most ancient lineages and the highest variation are underrepresented in the database.

Because of the database overrepresentation of some human populations, the distribution of pairwise distances is biased. A large part of pairwise comparisons are made between individuals belonging to the same population. Likewise, it is expected that most individuals from a single population will show similar distances to a given outgroup (Neandertal, in this case). To overcome this problem, we considered another sample of the human variation. We first sorted the HVI sequences in our data set according to it uncorrected distance to the reference sequence (Anderson et al. 1981). Then we grouped them into 171 classes, containing equidistant sequences (considering four decimals), and chose one sequence at random from each class. The computation of pairwise distances between 171 randomly selected sequences and the Neandertals rendered 1.6% of human-human comparisons larger than the smallest difference between Neandertals and humans. Likewise, 27% of the comparisons are lower than the largest human-human difference. This result suggests that Neandertals sequences are not so different from those of extant humans, in contrast to the NSG claims."

Guitierrez et al., went on to note that:

"The main conclusion can be extracted from our analyses: the phylogenetic position of the ancient DNA sequences recovered from Neandertal bones is sensitive to the phylogenetic methods employed. It depends on the model of nucleotide substitution, the branch support method, and the set of data used. Adcock et al. (2001) recovered HVI sequences of archaic human bones from Australia, and their phylogenic analysis showed that two of the specimens were outgroups even for the most ancient African lineages. They concluded that this is evidence supporting the multiregional hypothesis. However, a second analysis carried out by Cooper et al. (2001) that took into account the heterogeneity of rates between sites and a large sample of modern humans, showed that both HVI sequences are located among extant humans. This case illustrates the influence of the nucleotide substitution model on the phylogenetic reconstruction of the human D-loop region.

The NSG studies used poor parameter models of nucleotide substitution for their analysis, whereas we opted for complex (parameter rich) models following the likelihood ratio test. We believe that the likelihood mapping values supporting Neandertals as a different species might be artifactually increased."

Then problems with DNA sequence analysis are getting so bad that some scientists are suggesting that variable control regions in DNA not be used at all for reconstructing human genetic history. It simply has too many problems associated with it. 51 One problem is that mtDNA functions as a single genetic locus, as a single gene does in nuclear DNA. Studies that work off a single genetic locus are more likely to be affected by random genetic changes than are studies that include more than one locus (the more the better). Therefore, single locus studies are less accurate in characterizing a population. Another problem with mtDNA is that it is strictly limited to maternal inheritance. Because of this, genetic patterns that are drawn from mtDNA studies can differ from those that come from nuclear DNA studies. These differences could be quite misleading. 52

Another potential problem is the use of control regions as a "molecular clock". Some nucleotide regions mutate slowly, while others can mutate relatively rapidly. 53 These mutational "hotspots" can mutate fairly rapidly even with a single lifetime and are intuitively rather common in the aged. 54 Of course such "somatic" mutations arise in mitochondria of various bodily tissues and, unless they involve gametes, they are not passed on to the next generation. However, they would still affect phylogenetic interpretations. Scientists have tried to compensate for these problems, but the various methods have produced divergent results. 55 Also, direct comparisons of modern sequences with historical sequences often yield very difference results from those estimated by indirect methods that are based on present day sequence differences. For example, direct comparisons of modern penguins with historically sequenced penguins have shown that their mtDNA mutation rates are 2 to 7 times faster than had previously been assumed through indirect methods. 56 Direct studies with human mtDNA mutation rates are even worse, showing a discrepancy with previously estimated rates by as much as 20 fold. The "mitochondrial Eve", or the common ancestor of modern humans, was once thought to be about 150,000 years old. Based on the new rates of mitochondrial mutation, this figure might have to be reduced to as low as 6,500 years. 57 Consider the following comments published by Thomas Parsons in the journal Nature Genetics:

"The rate and pattern of sequence substitutions in the mitochondrial DNA (mtDNA) control region (CR) is of central importance to studies of human evolution and to forensic identity testing. Here, we report a direct measurement of the intergenerational substitution rate in the human CR. We compared DNA sequences of two CR hypervariable segments from close maternal relatives, from 134 independent mtDNA lineages spanning 327 generational events. Ten subsitutions were observed, resulting in an empirical rate of 1/33 generations, or 2.5/site/Myr. This is roughly twenty-fold higher than estimates derived from phylogenetic analyses. This disparity cannot be accounted for simply by substitutions at mutational hot spots, suggesting additional factors that produce the discrepancy between very near-term and long-term apparent rates of sequence divergence. The data also indicate that extremely rapid segregation of CR sequence variants between generations is common in humans, with a very small mtDNA bottleneck. These results have implications for forensic applications and studies of human evolution.

The observed substitution rate reported here is very high compared to rates inferred from evolutionary studies. A wide range of CR substitution rates have been derived from phylogenetic studies, spanning roughly 0.025-0.26/site/Myr, including confidence intervals. A study yielding one of the faster estimates gave the substitution rate of the CR hypervariable regions as 0.118 +- 0.031/site/Myr. Assuming a generation time of 20 years, this corresponds to

1/600 generations and an age for the mtDNA MRCA of 133,000 y.a. Thus, our observation of the substitution rate, 2.5/site/Myr, is roughly 20-fold higher than would be predicted from phylogenetic analyses. Using our empirical rate to calibrate the mtDNA molecular clock would result in an age of the mtDNA MRCA of only

6,500 y.a., clearly incompatible with the known age of modern humans. Even acknowledging that the MRCA of mtDNA may be younger than the MRCA of modern humans, it remains implausible to explain the known geographic distribution of mtDNA sequence variation by human migration that occurred only in the last

On top of this molecular clock problem, scientists are seem to have more problems agreeing that the mtDNA control regions are in fact "immune" from the pressures of natural selection. If it turns out that these control regions are not immune from such selection pressures, some scientists feel that this would allow Neandertals to be directly or even indirectly ancestor to modern humans. 58 In fact, recently published papers are suggesting that the Mezmaiskaya infant (one of the three Neandertal specimens that have yielded mtDNA) was actually not a Neandertal at all, but an "early modern human". 59 If this is true, this suggests that modern humans are just a different from Neandertals as we are from early modern humans. This supports the view that Neandertals, as well as early modern humans, were ancestral to us modern humans. According to this view, the differences between Neandertal mtDNA and our own mtDNA simply reflect the changes that have occurred in the mitochondrial genome since Neandertal times less than 50,000 years ago (based on radiometric dating). Of course, this is a far cry from the

600,000 year date suggested by those such as Krings et al.

Given all of these findings, what seems most reasonable? Are Neanderthals anything but human? It seems like they fall well within human ethnic variation. How then can we say that, based on such variations that Neanderthals belong to a different group or species than Homo sapiens? (Back to Top)

In 1937, Germaine Henri-Martin, a very well respected archeologist, began excavations in a cave in southwestern France called Fontechevade and continued her work here until 1954, removing over 900 cubic meters of sediment. When she first started excavating, the cave was pretty much filled with sediment with only a small crawlspace left to get into the cave. As she and her crew dug downward they found several layers. The topmost layers were "Aurignacian" and were thought to be laid down during the time of anatomically modern humans. Underneath the Aurignacian layers were the "Mousterian" layers, laid down during the time of the Neandertals. A bit more digging reveals the "Tayacian" layers within which she found several human skull fragments that, to her and many others like Henri Vallois (new director of the Institute of Human Paleontology), looked relatively modern with its lightly built structure and lack of browridges.

Of course, a modern looking human skull found in layers older than Neandertals would be quite something indeed. It certainly would and did disturb the paradigm of the day, but seemed to fit the predictions made by Marcellin Boule who removed Neandertals from the human family in 1908 and predicted that the true lineage leading to modern man would reach much farther back in time, bypassing Neandertals altogether. Many, with Boule, could not tolerate the idea of Neandertals being "human" because this would lessen human "specialness". In any case, Germaine's initial finds seem to confirm this hypothesis and so she was strongly encouraged by Vallois to keep digging to discover more about the life of the "earliest Frenchman."

Germaine did indeed discover plenty of evidence to very nicely flesh out a very good story of how the first French people lived. For example, the site is full of flint, which was interpreted as being worked into tools. Various "hearths" were also found throughout the site where the first families cooked, prepared their food, and ate. Evidence of these meals, in the form of animal bones, were everywhere. And, she found the hominids themselves, or at least their bones. So, the evidence for a rather complete an intricate life for the earliest French people seemed rather obvious and fairly easily interpreted.

After the1950s, the years rolled by without any similar finds of modern human remains below those of Neandertals. In the early 1970s, a young graduate student, Erik Trinkaus, started asking some questions. He found that the reason the skull fragments lacked browridges was because that area was completely broken off. Given this evidence, the interpretation of modern human features seemed to be based on little more than wishful thinking.

Now, everything was called into question - even the interpretation of the Fontechevade site itself. Shannon McPherron and Harold Dibble decided to do some reinvestigation with the aide of some higher technology - a very precise digital laser "theodolite" mapping system. With this system they were able to record the exact position and location of every object found during their dig. Over the next five years McPherron and Dibble collected and recorded data on thousands of stone objects and animal bones. After careful analysis of all the data sets, their conclusions were actually quite shocking.

Germaine had interpreted the flint stones as very "primitive" tools, even more primitive than those used by Neandertals. Little did she know how primitive these tools really were. As part of their research McPherron and Dibble noted that known manmade tools all have certain features, like a sharpened regular modification of a flint edge. None of the "tools" found out Fontechevade had such features. They were in fact indistinguishable from naturally broken rocks! The animal bones were problematic as well. They showed no signs of deliberate butchering and they were generally oriented in a parallel or perpendicular fashion with respect to the cave walls and to each other. Such orientation is not consistent with people randomly dropping these bones on the ground of the cave-home surface. They would have to be extraordinarily neat and unusual people indeed to place the remains of dinner in such neat alignment. Of course, such orientation is much more consistent with a watery deposition, and that is exactly what McPherron and Dibble concluded. When an object is being moved along by a stream, it either turns sideways and rolls with the flow or it turns perpendicular to the flow to let the water slip past with little resistance. After discovering this artifact orientation phenomenon, a source for the flowing water was searched for and found. The source was a narrow passage at the back end of the cave that worked to drain water from above, washing debris through the roof into the cave from the outside.

Obviously then, Germaine, and many of her colleagues, fell victim to wishful thinking, interpreting artifacts found in rather obvious fluvial deposition layers as evidence of the family life of early humans. The narrator of the 2002 PBS documentary, "Neanderthals on Trial" concluded:

"What made it look real to the archaeologists was an overwhelming desire to see the past in a certain way.

The urge to distance ourselves from Neanderthals or to pull them closer to us is a surprisingly powerful force./font>

Archaeologists Jean Philippe Rigaud and Jan Simek are well aware of the problem." [Jan Simek added], "I think that we're as guilty of it today, of that kind of preconceived approach to our data, as anybody has been in the history of archaeology or anthropology. It's almost inevitable that our own views of the world will be brought to bear." 68

It is also interesting to consider comments made by the journalist, Mark Davis, who investigated this story on Neanderthals for NOVA.

"Yes, it's fascinating to see how scientists unravel the story of human evolution. But if you venture into this world as a journalist, you must be prepared for the fact that there's a lot more raveling going on than unraveling.

There are many, many arguments in this famously contentious field, not about whether humans evolved, but how. . . I spoke with many Neanderthal experts in the course of making this film, and I found them all to be intelligent, friendly, well-educated people, dedicated to the highest principles of scientific inquiry. I also got the impression that each one thought the last one I talked to was an idiot, if not an actual Neanderthal.

Because people sometimes believe what they see on TV, especially public TV, the NOVA producer has an obligation to try to get things right. So which one of the experts should I have believed? The more people I spoke with, the more confusing it got. . . Listening to the archeologists and anthropologists talk about their work (and their colleagues' work), I heard the same frustrations voiced again and again: People are driven by their preconceptions. They see what they want to see. They find what they're looking for. . .

I learned that what people see in Neanderthals often has as much to do with philosophy as it does with science. What does it mean to be human? Some definitions are broad and inclusive, others are narrow and exclusive. Scholars have been known to attack one another's views on Neanderthals as "racist" or "politically correct." . . . What I found most interesting in all this is that every scientist I talked to encouraged me to explore the issue of self-delusion, and no one claimed to be immune. They are all aware that the history of the field is littered with brilliant scholars who completely missed the boat because of the power of their preconceptions." 69

An excellent example of a dating problem in the news appears in an article from National Geographic magazine. It describes some footprints made in volcanic ash that are said to be 3.6 million years old.

As I kneel beside the large print and lightly touch its sole, I am filled with quiet awe. It looks perfectly modern. "I thought that at three and a half million years ago their prints might be somehow different from ours," says Latimer. "But they aren't. The bipedal adaptation of those hominids was full-blown." 23

Mary Leakey discovered this 73-foot long trail of fossilized footprints consisting of 20 prints of an individual the size and shape of a modern 10-year-old human and 27 prints of a smaller person. The paleoanthropologist Timothy White, who was working with Leakey at the time, said:

"Make no mistake about it, they are like modern human footprints. If one were left in the sand of a California beach today, and a four-year old were asked what it was, he would instantly say that somebody had walked there. He wouldn't be able to tell it from a hundred other prints on the beach, nor would you. The external morphology is the same. There is a well shaped modern heel with a strong arch and a good ball of the foot in front of it. The big toe is straight in line. It doesn't stick out to the side like an ape toe" (Lucy p. 250, Johanson & Edey).

Louis Robins of the University of North Carolina who analyzed the footprints said:

"The arch is raised, the smaller individual had a higher arch than I do -- the toes grip the ground like human toes. You do not see this in other animal forms" (Science News 115:196-197, 1979).

In a recent lecture in St. Louis, Mary Leakey pointed out one additional feature of her footprints that one does not often see mentioned in the literature all of the larger footprints of the trail have a smaller footprint superimposed on them! Mary Leakey herself conceded that it appears that a child was intentionally lengthening its stride to step in an elder's footprints! In addition there were thousands of tracks of a wide variety of animals that are similar or identical to animals living in the area today including antelopes, hares, giraffes, rhinoceroses, hyenas, horses, pigs and two kinds of elephants. Even several birds' eggs were found and many of these could be easily correlated with eggs of living species.

Mary Leakey assumes that the footprints were made by some hominid but not by Homo sapiens because the stratum in which the prints are found is estimated to be 3.5 Ma. That happens to be the current presumed age ofA. afarensis and thus it is that Johanson insists that they simply would have to have been made by hisA. afarensis:

"The foot prints would have to be from A. afarensis. They substantiate our idea that bipedalism occurred very early, and our contention that the brain was too small to master tools."

Mary Leakey disagrees with Johanson and his claims forA. afarensis as the maker of her footprints. Mary Leakey is not the only one who questions Johanson's claims for Lucy. In a recent article, in Science News 122:116 titled, "Was Lucy a Climber", two groups of scientists, working independently, challenged the claim that Lucy had completely abandoned the trees and walked fully upright on the ground. Anthropologist Russel Tuttle from the University of Chicago said that the Laetoli footprints that Leakey discovered in Tanzania were made by another more human species of ape-man that coexisted withA. afarensis about 3.7 million years ago and that it was this unknown hominid that is the direct ancestor to man. After a careful examination of the Laetoli prints and foot bones of the Hadar A. afarensis, he concluded that, "The Hadar foot is ape-like with curved toes" whereas the footprints left in Laetoli are "virtually human."

Susman and Stern of the State university of New York at Stony Brook have concluded that A. afarensis, while capable of walking upright, spent considerable time in the trees. They base this conclusion on an examination of Lucy's scapula, foot and hand bones, which they say show, "unmistakable hallmarks of climbing." They also believe that Lucy's limb proportions did not allow an efficient upright gait.

Dr. David Pilbeam, an anthropologist from Harvard, make some very interesting comments in a 1978 review of Richard Leakey's book,Origins. Pilbeam said that it was, "A clear statement of our current consensus view of human evolution, and remarkably up to date." But, he concluded with the following sobering thoughts: "My reservations concern not so much this book but the whole subject and methodology of paleoanthropology. But introductory books - or book reviews - are hardly the place to argue that perhaps generations of students of human evolution, including myself, have been flailing about in the dark: that our data base is too sparse, too slippery, for it to be able to mold our theories. Rather the theories are more statements about us and ideology than about the past. Paleoanthropology reveals more about how humans view themselves than it does about how humans came about. But that is heresy." 19

APES UP FROM?, DONALD JOHANSON, "At any rate, modem gorillas, orangs and chimpanzees spring out of nowhere, as it were. They are here today they have no yesterday. LUCY, p.363

SUDDEN APPEARANCE: 'Biologists would dearly like to know how modern apes, modern humans and the various ancestral hominids have evolved from a common ancestor. Unfortunately, the fossil record is somewhat incomplete as far as the hominids are concerned, and it is all but blank for the apes. The best we can hope for is that more fossils will be found over the next few years which will fill the present gaps in the evidence.' The author goes on to say: 'David Pilbeam [a well-known expert in human evolution] comments wryly, "If you brought in a smart scientist from another discipline and showed him the meagre evidence we've got he'd surely say, 'forget it: there isn't enough to go on'."

(Richard E. Leakey, The Making of Mankind, Michael Joseph Limited, London, 1981, p. 43)

HAZARDOUS SURMISING: "The fossil record pertaining to man is still so sparsely known that those who insist on positive declarations can do nothing more than jump from one hazardous surmise to another and hope that the next dramatic discovery does not make them utter fools . Clearly some refuse to learn from this. As we have seen, there are numerous scientists and popularizers today who have the temerity to tell us that there is 'no doubt' how man originated: if only they had the evidence. "

(William R Fix, The Bone Pedlars, New York: Macmillan Publishing Company, 1984, p.150)

PROVEN ANCESTRY: RICHARD C. LEWONTIN, Prof. of Zoology, Harvard, "Look, I'm a person who says in this book [Human Diversity, 1982 that we don't know anything about the ancestors of the human species. All the fossils which have been dug up and are claimed to be ancestors we haven't the faintest idea whether they are ancestors. . All you've got is Homo sapiens there, you've got that fossil there, you've got another fossil there. and it's up to you to draw the lines. Because there are no lines.", Harpers, 2/84

RECONSTRUCTIONS: EARNST A. HOOTEN, Harvard, "To attempt to restore the soft parts is an even more hazardous undertaking. The lips, the eyes, the ears, and the nasal tip, leave no clues on the underlying bony parts. You can with equal facility model on a Neanderthaloid skull the features of a chimpanzee or the lineaments of a philosopher. These alleged restorations of ancient types of man have very little if any scientific value and are likely only to mislead the public. So put not your trust in reconstructions.", UP FROM THE APE, p.332

RECONSTRUCTIONS: W. HOWELLS, Harvard, "A great legend has grown up to plague both paleontologists and anthropologists. It is that one of men can take a tooth or a small and broken piece of bone, gaze at it, and pass his hand over his forehead once or twice, and then take a sheet of paper and draw a picture of what the whole animal looked like as it tramped the Terriary terrain. If this were quite true, the anthropologists would make the F.B.I. look like a troop of Boy Scouts.", MANKIND SO FAR, p. l38

THEORY DOMINATED DATA, DAVID PILBEAM, YALE, "I am also aware of the fact that, at least in my own subject of paleoanthropology, "theory" - heavily influenced by implicit ideas almost always dominates "data". . Ideas that are totally unrelated to actual fossils have dominated theory building, which in turn strongly influence the way fossils are interpreted." Quoted in BONES OF CONTENTION p.127

PARANORMAL ANTHROPOLOGY, LORD SOLLY ZUCKERMAN, "We then move right of the register objective truth into those fields of presumed biological science, like extrasensory perception or the interpretation of man's fossil history, where to the faithful anything is possible and where the ardent believer is sometimes able believe several contradictory things at the same time." BEYOND THE IVORY TOWER, p.19

BASIS OF "FAMILY TREE". ROGER LEWIN, Editor, Research News, Science, "The key issue is the ability correctly to infer a genetic relationship between two species on the basis of a similarity in appearance, at gross and detailed levels of anatomy. Sometimes this approach. can be deceptive, partly because similarity does not necessarily imply an identical genetic heritage: a shark (which is a fish) and a porpoise (which is a mammal) look similar?, BONES OF CONTENTION, 1987, p. 123

"APE MAN" OUT, ROGER LEWIN, Ed., Research News, Science, "The dethroning of Ramapithecus from putative first human in 1961 to extinct relative of the orangutan in 1982 is one of the most fascinating, and bitter, sagas in the search for human origins." BONES OF CONTENTION, 1987, p.86

"APES", Robert B. Eckhardt, Penn. State Univ., ". there would appear to be little evidence to suggest that several different hominoid species are represented among the Old World dryopithecine fossils. (Ramapithecus, Oreopithecus, Limnopithecus, Kenyapithecus). They themselves nevertheless seem to have been apes morphologically, ecologically, and behaviorally.", Scientific American, Vol.226, p.101

SECOND "APE MAN" OUT, ROGER LEWIN, Ed., Research News, Science, Richard and his parents, Louis and Mary, have held to a view of human origins for nearly half a century now that the line of true man, the line of Homo large brain, tool making and so on has a separate ancestry that goes back millions and millions of years. And the apeman, Australopithecus, has nothing to do with human ancestry." BONES OF CONTENTION, 1987, p.18

LEAKEY DEFECTION, "Dr. Leakey bases his repudiation of Darwin on the results of his long search in East Africa for the remains of the original man. The generally accepted post Darwin view is that man developed from the baboon 3 to 5 million years ago. But Leakey has found no evidence of a spurt in development at that time.", Chicago American, 1/25, 1967

DISMISSED APE, LORD SOLLY ZUCKERMAN, "His Lordship's scorn for the level of competence he sees displayed by paleoanthropologists is legendary, exceeded only by the force of his dismissal of the australopithecines as having anything at all to do with human evolution. 'They are just bloody apes', he is reputed to have observed on examining the australopithecine remains in South Africa.. Zuckerman had become extremely powerful in British science, being an adviser to the government up to the highest level. while at Oxford and then Birmingham universities, he had vigorously pursued a metrical and statistical approach to studying the anatomy of fossil hominids. it was on this basis that he underpinned his lifelong rejection of the australopithecines as human ancestors.", Roger Lewin, BONES OF CONTENTION, 1987, p.164, 165

DEFINITELY AN APE, LORD SOLLY ZUCKERMAN, "The australopithecine skull is in fact so overwhelmingly simian as opposed to human (figure 5) that the contrary proposition could be equated to an assertion that black is white.", BEYOND THE IVORY TOWER, p.78

UNHUMAN, LIKE THE ORANGUTAN, CHARLES E. OXNARD, Dean of Graduate School, Prof. of Biology & Anatomy, USC, ". conventional wisdom is that the australopithecine fragments are generally rather similar to humans. the new studies point to different conclusions. The new investigations suggest that the fossil fragments are usually uniquely different from any living form: when they do have similarities with living species, they are as often as not reminiscent of the orangutan, . these results imply that the various australopithecines are really not all that much like humans. . may well have been bipeds, . but if so, it was not in the human manner. They may also have been quite capable climbers as much at home in the trees as on the ground..", The American Biology Teacher, Vol.41, May 1979, pp.273-4

LIKE PYGMY CHIMP, ADRIENNE L ZIHLMAN, U. C. Santa Cruz, "Zihlman compares the pygmy chimpanzee to "Lucy," one of the oldest hominid fossils known and finds the similarities striking. They are almost identical in body size, in stature and in brain size. These commonalties, Zihlman argues indicate that pygmy chimps use their limbs in much the same way Lucy did. ", Science News, Vol.123, Feb.5. 1983, p.89

AUSTRALOPITHECINES, William Howells, Harvard, ". the pelvis was by no means modern, nor were the feet: the toes were more curved than ours the heel bones lacked our stabilizing tubercles and a couple of small ligaments that, in us, tighten the arch from underneath, were apparently not present. The finger bones were curved as they are in tree climbing apes." GETTING HERE, 1993, p.79

SHRIVELED STATUS, MATT CARTMILL, Duke DAVID PILBEAM Harvard GLYNN ISAAC Harvard "The australopithecines are rapidly shrinking back to the status of peculiarly specialized apes. ", American Scientist, (JulyAugust 1986) p.419

BELIEVE IT, SEE IT, ROGER LEWIN, Editor of Research News, Science, "How is it that trained men, the greatest experts of their day, could look at a set of modern human bones the cranial fragments and "see" a clear simian signature in them and see in an apes jaw the unmistakable signs of humanity. The answers, inevitably, have to do with the scientist's' expectations and their effects on the interpretation of the data. It is, in fact, a common fantasy, promulgated mostly by the scientific profession itself, that in the search for objective truth, data dictate conclusions. If this were the case, then each scientist faced with the same data would necessarily reach the same conclusion. But as we've seen earlier and will see again and again, frequently this does not happen. Data are just as often molded to fit preferred conclusions.", BONES OF CONTENTION, pp.61, 68

EVOLUTION OR VARIATION? ". a Neanderthaler is a model of evolutionary refinement. Put him in a Brooks Brothers suit and send him down to the supermarket for some groceries and he might pass completely unnoticed. He might run a little shorter than the clerk serving him but he would not necessarily be the shortest man in the place. He might be heavier-Featured, squattier and more muscular than most, but again he might be no more so than the porter handling the beer cases back in the stock room." EVOLUTION, TimeLife Nature Library.

LARGER BRAIN, WILLIAM HOWELLS, Harvard, "The Neanderthal brain was most positively and definitely not smaller than our own indeed, and this is a rather bitter pill, it appears to have been perhaps a little larger.", MANKIND SO FAR, p.165

MODERN CAME FIRST, O. BARYOSEF, Peabody Museum, Harvard, B. VANDERMEERCH, Univ. Bordeaux, "Modern Homo sapiens preceded Neanderthals at Mt. Carmel. . modern looking H. sapiens had lived in one of the caves some 50,000 to 100,000 years ago, much earlier than such people had been thought to exist anywhere. . The results have shaken the traditional evolutionary scenario, producing more questions than answers." Scientific American, p.94, April 1993

RUINED FAMILY TREE, "Either we toss out this skull [1470] or we toss out our theories of early man," asserts anthropologist Richard Leakey of this 2.8 million year old fossil, witch he has tentatively identified as belonging to our own genus. "It simply fits no previous models of human beginnings." The author, son of famed anthropologist Louis S. B. Leakey, believes that the skull's surprisingly large braincase "leaves in ruins the notion that all early fossils can be arranged in an orderly sequence of evolutionary change.", National Geographic, June 1973, p.819

HUMAN BRAIN, "Leakey further describes the whole shape of the brain case [1470] as remarkably reminiscent of modern man, lacking the heavy and protruding eyebrow ridges and thick bone characteristics of Homo erectus." Science News, 102 (4/3/72) p.324

HUMAN BRAIN, Dean Falk, St. U. of N.Y. at Albany, ". KNMER 1805 Homo habilis should not be attributed to Homo. the shape of the endocast from KNMER (basal view) is similar to that from an African pongid, where as the endocast of KNMER 1470 is shaped like that of a modern human." Science, 221, (9/9/83) p.1073

HUMAN BRAIN "The foremost American experts on human brain evolution Dean Falk of the State University of New York at Albany and Ralph Holloway of Columbia University usually disagree, but even they agree that Broca's area is present in a skull from East Turkana known as 1470. Philip Tobias. renowned brain expert from South Africa concurs." Anthro Quest: The Leakey's Foundation News. No.43 (Spring 91) p.13

NOT ERECTUS, "According to paleoanthropologist Ian Tattersall of the American Museum of Natural History in New York the African skulls. assigned to erectus often lack many of the specialized traits that were originally used to define that species in Asia, including the long low cranial structure thick skull bones, and robustly built faces. In his view, the African group deserves to be placed in a separate species. " Discover, 9/94, p.88

"OLD" MODERN MEN, Louis Leakey, 'In 1933 I published on a small fragment of jaw we call Homo kanamensis, and I said categorically this is not a nearman or ape, this is a true member of the genus Homo. There were stone tools with it too. The age was somewhere around 2.5 to 3 million years. It was promptly put on the shelf by my colleagues, except for two of them. The rest said it must be placed in a 'suspense account.' Now, 36 years later, we have proved I was right." Quoted in BONES OF CONTENTION, p.156

'THE OLDEST MAN', "[African Footprints] . they belonged to the genus Homo (or true man), rather than to manapes (like Australopithecus, who was once a thought to be the forerunner of man but is now regarded as a possible evolutionary dead end). . they were 3.35 million to 3.75 million years old. . they would, in Mary Leakeys words, be people 'not unlike ourselves,'. " Time, Nov. 10, 1975, p.93

TOO HUMAN TOO OLD, Russel H. Tuttle, Professor of Anthropology, University of Chicago, Affiliate Scientist, Primate Research Center, Emory University, "In sum, the 3.5millionyearold footprint trails at Laetoli sight G resemble those of habitually unshod modem humans. If the G footprints were not known to be so old, we would readily conclude that they were made by a member of our genus. in any case we should shelve the loose assumption that the Laetoli footprints were made by Lucy's kind. " Natural History, 3/90, p.64.

MODERN & TALL, RICHARD LEAKEY, . the boy from Turkana was surprisingly large compared with modern boys his age he could well have grown to six feet. . he would probably go unnoticed in a crowd today. This find combines with previous discoveries of Homo erectus to contradict a long held idea that humans have grown larger over the millennia.", National Geographic, p.629, Nov., 1985

CHARLES E. OXNARD Dean, Grad. School, Prof. Bio. and Anat., USC, ". earlier finds, for instance, at Kanapoi. existed at least at the same time as, and probably even earlier than, the original gracile australopithecines. almost indistinguishable in shape from that of modern humans at four and a half million years. " American Biology Teacher, Vol.41, 5/1979, p.274.

HENRY M. MCHENRY, U. of C., Davis, "The results show that the Kanapoi specimen, which is 4 to 4.5 million years old, is indistinguishable from modern Homo sapiens. " Science Vol.190, p.

WILLIAM HOWELLS, Harvard, ". with a date of about 4.4 million, [KP 271] could not be distinguished from Homo sapiens morphologically or by multivariate analysis by Patterson and myself in 1967 (or by much more searching analysis by others since then). We suggested that it might represent Australopithecus because at that time allocation to Homo seemed preposterous, although it would be the correct one without the time element.", HOMO ERECTUS, 1981, p.79-80.

EVE KICKED OUT, STEPHEN J. GOULD, ". 'mitochondral Eve' hypothesis of modern human origins in Africa, suffered a blow in 1993, when the discovery of an important technical fallacy in the computer program used to generate and assess evolutionary trees debunked the supposed evidence for an African source. disproving the original claim.", Natural History, 2/94, p.21

"Differences due to age are especially significant with reference to the structure of the skull in apes. Very pronounced changes occur during the transition from juvenile to adult in apes, but not in Man. The skull of a juvenile ape is somewhat less different in shape from that of Man. We may remember that the first specimen ofAustralopithecus that was discovered by Raymond Dart, the "Tuang child", was that of a juvenile [ape]. This juvenile skull should never have been compared to those of adult apes and humans.? 16

A few miles to the east of Olduvai Gorge, in the forests of Zaire, are the Mbuti people who are on average only four feet to four feet six inches tall. These people are, in stature, brain capacity, and even way of life, are comparable to Homo habilis. Yet the Mbuti people are modern men in every sense.? 7

Small stature in humans is known to produce abnormal anatomical characteristics, which resemble ape-like characteristics, such as the jaw and dentition (because the individuals have the same number of teeth as us in a much more confined space) and the length of the arms. That is why many pygmy faces look different to ours (often showing prognathous teeth and jaws). Here is Francis Huxley: "In both types [of pygmy] the eyes tend to bulge, the upper jaw juts out, and the arms are longer than the legs." 17 Here is anthropologist David Davies: "There are two types [of prognathism] alveolar prognathism, which is restricted to the tooth region, and facial prognathism, which affects a much larger area of the face causing it to jut out, so increasing the facial area. A small chin is characteristic of both conditions. Prognathism is considered a primitive feature, particularly as it is most commonly found in apes and ancient primitive men. The Andamanese [pygmies] have pronounced prognathism."18 These descriptions are like the Australopithecine characteristic described above. This thinking lead Huxley and Darwin to mistakenly consider the Australian Aborigine as "primitive" because they have some of these features? although they are actually modern humans. 7

One of the most distinguished living palaeoanthropologists, Philip Tobias (1970), quotes the discoverer of Australopithecus, Raymond Dart, as saying that, "apparently normal human beings have existed with brain-sizes in the 700s and 800s" and that the smallest cranial capacity ever documented for a non-pathologic human is 790cc. 7

There is scientifically no basis in evidence for suggesting that intellectual capacity is correlated with brain size as is sometimes suggested and there is evidence which indicates such a view is mistaken (the systematic differential between human male and female brain capacity which is not reflected in the

Different medical anomalies, such as proportionate dwarfism, can result in very small adult humans with normal intelligence even though, with a proportionate head, cranial capacities can be less than 500 - 600cc. The shortest mature human male, of whom there is independent evidence, is Gul Mohammed (born 15 Feb 1957) of New Delhi, India. On 19 Jul 1990 he was examined at Ram Manohar Hospital, New Delhi, and found to measure 22 1/2in (57 cm) in height (weight 17kg 371/2lb). The other members of his immediate family are of normal height. For a time, the shortest ever female was Pauline Musters ('Princess Pauline'), a Dutch dwarf. She was born at Ossendrecht on 26 Feb 1876 and measured 12in 30cm at birth. At nine years of age she was 55 cm (21.65in) tall and weighed only 1.5kg (3lb 5oz). She died of pneumonia with meningitis on 1 Mar. 1895 in New York City, USA at the age of 19. A post mortem examination showed her to be exactly 24in (61 cm) (there was some elongation after death). Her mature weight varied from 7 1/2 - 9lb (3.4 - 4kg) and her 'vital statistics' were 18 1/2 - 19 - 17in (47 - 48 - 43cm), which suggests she was overweight (Guinness Book of World Records, Page 56). At the age of 17, "Princess Lucy" stood 21 inches high and weighted 14lbs, and was proportional in every way. Likewise, at the age of 20, Henrietta Moritz stood 22in. tall and weighed 36lbs. At the age of 32, the proportional CPT Jack Barnett stood 27in. tall and weighed in at a chubby 28 lbs. All were of at least average intelligence (Pictures can be seen at -1999).

1. J.S. Weiner, K.P. Oakley and W. E. Le Gros Clark, "Bulletin of the British Museum" (Natural History), Geological Series, Vol. 2, No. 3,The Solution of the Piltdown Problem, November 25, 1953.

2. Blinderman, Charles, The Curious Case of Nebraska Man, Science, June 1985, pp. 47-49.

3. Pilbeam, David, Science, April 6-7, 1982.

4. Zuckerman, Solly, Evolution as a Process, 1954.

5. Stern and Sussman, American Journal of Physical Anthropology, 60:279-313.

6. Oxnard, Charles, Fossils, Teeth and Sex: New Perspectives on Human Evolution, University of Washington Press, 1987.

7. Milton, Richard, Shattering the Myths of Darwinism, 1997.

8. Wendt, H. From Ape to Adam, 1972, pp 167-168.

9. Richard Leaky, American Scientist 64:174, 1976.

10. David N. Menton, Ph.D., Missouri Association for Creation, Inc., 1991.

11. Dr. Robert Eckhardt, Scientific American, 226: 94, 1972.

12. Louis Leaky, Science News of 1971 (100:357)

13. Fitch & Miller, Nature 226:226-228,1970.

14. Dalrymple and Lanphere, Potassium-Argon Dating, Principles, Techniques and Applications to Geochronology, pp. 197.

15. Jane Oppenheimer, Essays in the History of Embryology and Biology, p.50.

16. Duane Gish, Evolution: The Challenge of the Fossil Record, 1985, p. 178.

17. Francis Huxley, Peoples of the World, 1971.

18. David Davies, A Dictionary of Anthropology, 1972.

19. David Pilbeam, Review of Richard Leakey's bookORIGINS, American Scientist, 66:379, May-June 1978.

20. M. Boule, Fossil Men: Elements of Human Paleontology, 1923.

21. Johanson, Donald, as quoted in "Letters to Mr. Jim Lippard", Institute of Human Origins, Aug. 8, 1989 May 30, 1990.

22. Henri Vallois, new editions of Boule's (1921,1923) book Les Hommes Fossiles (Fossil Men), Boule and Vallois 1946, 1952.

23. Gore, R. National Geographic, Feb. 1997, "The First Steps", pp 72-99.

24. Lubenow, Marvin L., Bones of Contention, Appendix: "The Dating Game"

25. Krings, M., Stone, A., Schmitz, R.W., Krainitzki, H., Stoneking, M. and Svante Pääbo , S., 1997. Neandertal DNA sequences and the origin of modern humans. Cell, 90:19-30. ( Link )

26. Johanson, D. and Shreeve, J., 1989. Lucy's Child, William Morrow and Company, New York, p.49.

27. Lindahl, T., 1993. Instability and decay of the primary structure of DNA. Nature, 362:713.

28. Pääbo S., 1993. Ancient DNA, Scientific American, November 1993, p. 92.

29. Gibbons, A., 1998. Ancient history, Discover, January 1998, p. 47

30. Pääbo , S., Cooper, A., Poinar, H.N., Radovcic, J., Debenath, A., Caparros, M., Barroso-Ruiz, C., Bertranpetit, J., Nielsen-Marsh, C., Hedges, R.E.M. And Sykes, B., 1997. Neandertal genetics. Science, 277 (22 August 1997) 1021-1023.

31. Kahn, P. and Gibbons, A., 1997. DNA From an extinct human. Science, 277:176-177.

32. Lubenow, Marvin. Recovery of Neandertal mtDNA: An Evaluation. Creation Ex Nihilo Technical Journal 12(1):87-98, 1998

33. Gibbons, A. Calibrating the Mitochondrial Clock, Science 279, Volume 279, Number 5347 Issue of 2 Jan 1998, pp. 28, 29

34. Collins, F., M. Guyer, and A. Chakravarti,Variations on a Theme: Human DNA Sequence Variation, Science 278:1580-1581, 28 November 1997, page 1581.

35. Melnick, D. and Hoelzer, G., 1992. What in the study of primate evolution is mtDNA good for? American Journal of Physical Anthropology, Supplement 14, p. 122.

36. Marks, J., Chromosomal evolution in primates. The Cambridge Encyclopedia of Human Evolution, S. Jones, R. Martin, and D. Pilbeam (eds), Cambridge University Press, Cambridge, p. 302., 1992

37. Brand, Leonard. Faith, Reason, and Earth History. Andrews University Press, Berrien Springs, MI. , 1997.

38. Richmond, B.G. and Strait, D.S., Evidence that humans evolved from a knuckle-walking ancestor, Nature 404(6776):382-385, 2000.

39. Stokstad, E., Hominid ancestors may have knuckle walked, Science 287(5461):2131, 2000.

40. Collard, M. and Aiello, L.C., From forelimbs to two legs, Nature 404(6776):339-340, 2000.

41. Osborn H.F., Hesperopithecus, the anthropoid primate of western Nebraska. Nature, 110:281-3., 1922

42. Smith G.E., Hesperopithecus: the ape-man of the western world. Illustrated London News, 160:942-4., 1922

43. Wolf J. and Mellett J.S., The role of "Nebraska man" in the creation-evolution debate. Creation/Evolution, Issue 16:31-43., 1985

44. Spoor F., Wood B.A., and Zonneveld F., Implications of early hominid labyrinthine morphology for evolution of human bipedal locomotion. Nature, 369:645-8., 1994

45. Covey, Jon., Fossil Men: Part III, (from: Edited by Anita Millen, MD, MPH, MA., 1994

46. Ovchinnikov I.V., Götherström A ., Romanova G.P., Kharitonov V.M., Lidén K., and Goodwin W. (2000): Molecular analysis of Neanderthal DNA from the northern Caucasus. Nature, 404:490-3.

47. Höss, Matthias (2000): Neanderthal population genetics. Nature, 404:453-4.

48. Krings M., Capelli C., Tschentscher F., Geisert H., Meyer S., von Haeseler A. et al. (2000): A view of Neandertal genetic diversity. Nature Genetics, 26:144-6.

49. Krings, M., Geisert, H., Schmitz, R., Krainitzki, H., and Pääbo , S. DNA sequence of mitochondrial hypervariable region II from the Neandertal type specimen. Evolution, Proc. Natl. Acad. Sci. USA, Vol. 96, pp. 5581-5585, May, 1999.

50. Gutierrez, G., Sanchez, D., Marin, A. A Reanalysis of the Ancient Mitochondrial DNA Sequences Recovered from Neandertal Bones, Molecular Biology and Evolution, 19(8):1359-1366. 2002.

51. Ingman, Max, Henrik Kaessmann, Svante P 䤢 o, and Ulf Gyllensten (2000) "Mitochondrial genome variation and the origin of modern humans." Nature 408: 708-713.

52. Williams, Sloan R., Napoleon A. Chagnon, and Richard S. Spielman (2002) "Nuclear and mitochondrial genetic variation in the Yanomam: test case for ancient DNA studies of prehistoric populations." American Journal of Physical Anthropology 117: 246-259.

53. Stoneking, Mark (2000) "Hypervariable sites in the mtDNA control region are mutational hotspots." American Journal of Human Genetics 67: 1029-1032.

54. Nekhaeva, E., N.D. Bodyak, Y. Kraytsberg, S.B. McGrath, N.J. Van Orsouw, A. Pluzhnikov, J.Y. Wei, J. Vijg, and K. Khrapko (2002) "Clonally expanded mtDNA point mutations are abundant in individual cells of human tissues." Proceedings of the National Academy of Sciences 99: 5521-5526.

55. Heyer, Evelyne, Ewa Zietkiewicz, Andrzej Rochowski, Vania Yotova, Jack Puymirat, and Damian Labuda (2001) "Phylogenetic and familial estimates of mitochondrial substitution rates: Study of control region mutations in deep-rooting pedigrees." American Journal of Human Genetics 69: 1113-1126.

56. Lambert, D.M., P.A. Ritchie, C.D. Millar, B. Holland, A.J. Drummond, and C. Baroni (2002) "Rates of evolution in ancient DNA from Adélie penguins." Science 295: 2270-2273.

57. Parsons, Thomas J. A high observed substitution rate in the human mitochondrial DNA control region, Nature Genetics vol. 15, April 1997, pp. 363-367

58. Adcock, Gregory J., Elizabeth S. Dennis, Simon Easteal, Gavin A. Huttley, Lars S. Jermiin, W. James Peacock, and Alan Thorne (2001a) "Mitochondrial DNA sequences in ancient Australians: Implications for modern human origins." Proceedings of the National Academy of Sciences 98: 537-542.

59. Hawks, John and Milford H. Wolpoff (2001) "Paleoanthropology and the population genetics of ancient genes." American Journal of Physical Anthropology 114: 269-272.

60. Leakey, Mary, Interview, Associated Press (AP) Dec. 10, 1996.

61. Mehlert, A.W., "The Rise and Fall of Skull KNM-ER 1470", Creation Ex Nihilo Technical Journal, Vol. 13, No. 2 March 10, 2002 ( )

62. Excerpted from the technical article, "Problems with Distant Horizons," published at the ESREL'96 - PSAMIII Conference in Crete, 1996. (

63. Bromage, Tim , "Faces From the Past," New Scientist, vol. 133, issue 1803, 11 January 1992, p. 41. ( )

64. Bernard Wood, Mark Collard, "The Human Genus," Science, vol. 284, No 5411, 2 April 1999, pp. 65-71.

65. Fred Spoor, Bernard Wood & Frans Zonneveld, "Implications of Early Hominid Labyrinthine Morphology for Evolution of Human Bipedal Locomotion," Nature, vol 369, 23 June 1994, p. 645-648. ( )

66. Shan Mohammed, University of Toronto ( ), accessed March 7, 2004.

69. Mark Davis, "Into the Fray: The Producer's Story" from "Neanderthals on Trial" PBS Airdate: January 22, 2002 ( )

70. Ramapithicus: The Free Dictionary by Farlex, Columbia Electronic Encyclopedia, accessed 10/8/2005 (Link)

71. Johanson and Edgar, From Lucy to Language, Simon & Schuster, 1996, page 170

72. Mark Isaac (editor), Index to Creationist Claims, Claim CD031, 2005 ( )

73. Henry Fairfield Osborn, The Evolution of Human Races, Natural History, Jan/Feb. 1926. Reprinted in Natural History 89 (April 1980): 129.

74. F. Spoor, M. G. Leakey, P. N. Gathogo, F. H. Brown, S. C. Antón, I. McDougall, C. Kiarie, F. K. Manthi & L. N. Leake, Implications of new earlyHomo fossils from Ileret, east of Lake Turkana, Kenya, Nature, Vol. 448 (7154), pp. 688 (August 9, 2007) (Link)

Two fossils discovered in Kenya cast doubt on theories of the early evolution of the genus Homo. They show that the species H. habilis andH. erectus - previously thought to have evolved one after the other - actually lived side-by-side in eastern Africa for almost half a million years.

See Also: Borenstein, Seth, Fossils Change Old Evolutionary Theory, AP Science Writer, August 8, 2007 (Link)

75. Rak Y, Ginzburg A, Geffen E., "Gorilla-like anatomy on Australopithecus afarensis mandibles suggests Au. afarensis link to robust australopiths", Proc Natl Acad Sci U S A. 2007 Apr 17104(16):6568-72. Epub 2007 Apr 10. ( Link )

76. Henry Fairfield Osborn, The Evolution of Human Races, Natural History , Jan/Feb. 1926. Reprinted in Natural History 89 (April 1980): 129.

Note: Since these are my rough thoughts in draft from, I have not personally reviewed all of the above original references for accuracy of content. If errors are found, notification of such errors would be appreciated at:[email protected]

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Powers and Abilities


Symbiote Biology: Even without a host, the Venom symbiote is capable of freely extending its biomass into tentacles and tendrils, and usually manifests a fanged mouth and large white eyespots. It can also manifest a humanoid head, torso, and arms and after being cleansed became able to take on humanoid form without a host for brief periods. When bonded to a host, it can shapeshift to mimic any type of clothing whatsoever, as well as blending Venom in with his surroundings, rendering him invisible. The symbiote has augmented all of its host's physical abilities to superhuman levels equal to, and in some cases greater than, Spider-Man's.

Spider-Man (Peter Parker): While not the symbiote's first host or even its first human host, Peter Parker nevertheless had the most profound impact on the symbiote and its powerset. In addition to augmenting Peter's physical abilities when bonded to him, the symbiote interfaced with his genetic code and imprinted most of his powers into itself. 𖏺] The symbiote retained these copied powers even after separating from Peter, and bestowed them on its subsequent hosts.

  • Body Storage: Peter Parker was able to use the symbiote to store his camera and rolls of film. 𖑏] Flash often utilized the symbiote to withhold and store munitions and equipment through dimensional apertures within the suit. Wherein he could store foreign objects while keeping a sleek, aerodynamic profile. 𖑐] Having used this quality to store a live grenade within his body while keeping it from exploding. ⎨]
  • Camouflage Capabilities: The symbiote is capable of shapeshifting to mimic the appearance of any form of clothing, can camouflage with its surroundings to appear invisible, and can even mimic the appearance of other people. Peter Parker only used the former ability during the brief period he was bonded to it, while Brock's preferred form of clothing was a black shirt, jacket and pants.
  • Constituent-Matter Generation: The symbiote can use the living abyss comprising its matter to generate tendrils and pseudopods, and can use this for lethal effect against criminals. While Spider-Man was unaware it possessed this ability and did not consciously use it, Eddie Brock and its subsequent hosts would often use this ability offensively, such as by sending a part of the symbiote into a victim's body to smother them from the inside. 𖑑]
  • Parasitic Inheritance: The symbiote can copy the powers and abilities of other beings by interfacing with their genetic code, and primarily utilizes the spider powers it adapted from Spider-Man. [citation needed]
  • Wall-Crawling: The alien costume replicated Spider-Man’s ability to cling to walls by controlling the flux of inter-atomic attraction between molecular boundary layers. [citation needed]
  • Webbing Generation: The symbiote can convert its constituent matter into strands of white or black webbing, which it can shoot from the white patches on the back of its hands at high pressure up to a distance of 70 feet. The alien’s substance seems to be composed of tough, flexible fibers of organic polymers, which regenerate swiftly after "shedding." The strands have extraordinary adhesive properties, which diminish rapidly once they abandon their living source. After about three hours, with no source to nourish them, the strands dry up like dead skin and dissolve into a powder. The strands possess a tensile strength of 125 pounds per square millimetre of cross-section. The one limitation to this ability was used to Spider-Man's advantage during his second bout with Venom: Since the webbing itself is comprised of the symbiote's constituent matter, if Venom generates too much he will be left vulnerable as the symbiote is weakened and unable to replenish its lost mass for a short period of time. [citation needed]

Venom (Eddie Brock): The third human individual to bond with the symbiote was Edward Brock. Naturally, the symbiote chose to endow Eddie with most of the powers Spider-Man had, but via Brock's innovative mentality the symbiote has managed to create some new powers and even mutate over time. [citation needed] After Knull attempted to assimilate the Venom symbiote into the Grendel, its abilities were augmented and it acquired new powers while connected to Knull's hive-mind. 𖐖] After being reborn through the living abyss of a symbiote-dragon and Eddie becoming the new God of the Symbiotes after vanquishing Knull, the Venom symbiote's powers have been augmented to an unknown degree. 𖐴] 𖐵]

  • Superhuman Strength: Before he came into contact with the costume, Brock had conditioned himself to lift (press) 700 lb. 𖑒] Once they merged, the costume added Spider-Man’s superhuman strength to Brock’s vast human strength, making him more powerful than Spider-Man. However, his full strength often fluctuates. Venom has demonstrated strength ranging from only slightly greater than Spider-Man's to being capable of trading blows with high-powered individuals such as Juggernaut. This is caused by the several mutations that the symbiote took with Brock, gaining additional bulk and muscle mass over long periods of time with its host. [citation needed]
  • Superhuman Durability: Venom's body is highly resistant to physical injury, capable of withstanding assault from high-caliber bullets as well as attacks from super powered individuals. When distributed at a typical thickness over Brock's body, the symbiote is capable of absorbing bullets from small-arms weapons firing conventional ammunition. The symbiote is however particularly vulnerable to both sonic and heat-based attacks. [citation needed]
  • Superhuman Stamina: Venom is also capable of surviving in harmful areas for long periods of time such as underwater or in toxic gases, the symbiote filtering breathable air to the host. [citation needed]
  • Regenerative Healing Factor: Additionally, the symbiote is capable of healing injuries in the host at a faster rate than normal human healing allows. The symbiote is also capable of healing injuries and illnesses that current human medical care cannot such as cancer. The symbiote has enabled its host to recover from injuries that should have been lethal, such as Mac Gargan being impaled by the Swordsman's Makluan Sword 𖑓] and Flash Thompson being impaled by Toxin's blade-arm, 𖑔] and having his head sliced in half by Jack O'Lantern V's scythe. 𖑕]
  • Genetic Memory: The symbiote possesses some psychic ability, making it capable of obtaining information from its hosts and even other people and symbiotes simply by touch The symbiote is capable of recalling information from previous hosts. This ability allowed Eddie Brock to know the secret identity of Spider-Man when the symbiote bonded with him. It can however, be forced to forget information if the symbiote is inflicted with heavy trauma. [citation needed]
  • Offspring Detection: The symbiote is also capable of psychically detecting its offspring, however with effort this ability can be blocked. [citation needed]
  • Body Chemistry Manipulation: In order to gaslight Eddie into believing he had terminal cancer, the Venom symbiote altered his biochemistry to simulate the symptoms. 𖑖] After being temporarily reconnected to Knull's hive mind, the symbiote gained the ability to directly affect the neurochemical functions within its host in order to induce various psychological effects, such as calmness, sleep, or even memory suppression. 𖐖]
  • Telepathy: The Klyntar species communicate both psionically and biochemically with the host and each other. Their powers of the mind initially start out as weak without a host to bond to. [citation needed] Venom's years fused to Eddie Brock had more than strengthened its lingering psychic powers to the point its screams of anguish could be felt across all of New York. ⏑] While indwelled by a demon, Agent Venom employed this creatively through his tendrils to seize control of an army of mercenaries. 𖑗] After coming into contact with Knull, the symbiote displayed the ability to telepathically communicate with other symbiotes. 𖐖]
  • Constituent-Matter Manipulation: While the symbiote did not use this ability frequently when bonded to Eddie Brock, it was capable of transforming parts of its host's body: it once morphed Venom's hands into scythe-like hooks and sword-like blades during a battle against Nova, and turned his arms into bat-like wings to let him glide. 𖑘] After being augmented by Knull, the symbiote developed the ability to manifest wings resembling those of the Grendel symbiote-dragon in order to fly. 𖐖] Venom could also project its biomass into a multi-layered shield to better withstand powerful attacks. 𖑙] When bonded to Mac Gargan, it used this ability to grow a tail, emulating Gargan's appearance as the Scorpion. 𖑚] When bonded to Flash Thompson, the symbiote regularly displayed the ability to morph sections of Agent Venom's body, such as his hands or feet, into spikes, blades, axes or a shield. [citation needed]
  • Digital Immersion: In a battle with its offspring Carnage, the Venom symbiote and its host displayed the ability to physically enter into the Internet on a “molecular level” and travel between hard-wired computers through Ethernet cables. 𖑛]
  • ESP: Although the Venom symbiote does not possess a spider-sense, 𖑜] it possesses a similar extrasensory ability. This response is not as complicated as Spider-Man’s inherent sense since the alien costume can detect danger from every direction and conduct Brock in plenty of time. It's a lot more efficient than Spider-Man’s spider-sense because it takes less time to sense the danger, and Brock’s reflexes are faster than Spider-Man’s, even when they are enhanced by the alien costume for instance, Venom can dodge a gunshot or a barrage of bullets. [citation needed]
  • Empathetic Empowerment: The Venom symbiote, like others of its kind, is capable of feeding off its host's negative emotions - chiefly rage, hatred, and bloodlust - in order to augment itself. However, doing so has a corrupting effect on the symbiote, causing it to become increasingly bloodthirsty, cruel, and feral. 𖑅]⎛]𖏷]
  • Klyntar Assimilation: In a similar manner to how the Hybrid symbiote was formed, Venom is capable of amalgamating with other symbiotes in order to bolster their shared power. It merged with its clone, increasing its strength by an unknown degree ⏣] and amalgamated with Rex Strickland's symbiote in order to become powerful enough to face Knull and the Grendel symbiote. 𖐖]
  • Immunity to Spider-Man's Spider-Sense: Due to Spider-Man being a host to the symbiote, Venom, and his offspring, are able to bypass Spider-Man's spider-sense. Venom is capable of attacking Spider-Man without alerting him, making Venom a deadly foe. It should be noted that as Ben Reilly was cloned from Peter before he bonded with Venom, Eddie was not immune to his spider-sense. [citation needed]
  • Poisonous Fangs: An ability developed by Eddie Brock upon bonding with the symbiote. Originally he commanded the symbiote to sprout a maniacal grin and tongue, differentiating him from Spider-Man. Later it was revealed that this set of fangs not only intimidates foes but can deliver a powerful, venomous bite (true to Brock's namesake). This bite was able to cripple the Sandman, eventually leaving the villain-turned-hero unable to reform himself properly and almost causing his death. 𖑝]
  • Stretching and deforming: Although it's widely known that the symbiote can stretch and deform itself, recently it was able to perform this ability while bonded with a human host. Venom can expand to any size as long as they have something to grow on such as a host or an object. Symbiotes can get inside of small areas such as electric wires and the insides of cars and completely disable them. [citation needed]
  • Telepathy Resistance: As a result of Venom being a bond between two separate minds, it takes longer than conventional for a telepath to affect its mind. This defense is not absolute, however. 𖐊] Additionally, attempting to telepathically incapacitate Venom by targeting the host does not prevent the symbiote from fighting back. ⎾]
  • Energy Absorption & Transference: After connecting to the Symbiote Hive-Mind of Earth-1051, the symbiote displayed the power to channel energy and fire it back at the opponent by morphing its arms into energy cannons, similar to its Earth-23203 counterpart. 𖐮] However, once it disconnected from Earth-1051's hive-mind it lost this ability. 𖑞]

Malekith: After capturing the Venom symbiote, 𖐢] the dark elf warlord Malekith bent it to his will using dark magic and the arcane ambiance of Stonehenge in England, bonding with it to increase his own combat prowess. 𖑟]

  • Symbiotic Expansion and Psychic Control: Through Venom, Malekith could extend his symbiote to others and interlink them to his own being. Wielding his warriors like a puppet armed force which he could further guide and enhance with symbiote like abilities of they're own. Ε]
  • Constituent-Matter Manipulation: Like many users of the symbiote species, Malekith can conjure and utilize symbiote biomass in order to create his own colorful arsenal physiological extremities. The likes of razor-sharp or blunt-force melee weaponry, large batlike wings to fly with, or simply transforming the symbiote itself into a metamorphic blade. 𖑠]
  • Dark Magic Enhancement: Through his connection with one of Knull's creations, Malekith found that his own arcane abilities were greatly enhanced many times over, making both him and the Klyntar he'd bonded to powerful enough to trade blows with four iterations of the God of Thunder single handed. Ε]
  • Stretching and deforming: To a limited extent Malekith could utilize the amorphous properties of the Venom Symbiote to further enhance himself having used it elongate his tongue into a lethal razor whip he can fight with. Ε]

Agent Venom (Flash Thompson): After the US military bonded the symbiote to Flash Thompson as the fourth host of the symbiote, it displayed all of the above abilities as well as developing a few new ones as a result of being connected to the Klyntar hive mind.

  • Hive Mind: After being purged of its bloodlust, the symbiote gained access to the Klyntar hive mind, enabling it to communicate with the symbiotes on their homeworld and access information about the species' past. ⎪]
  • Cosmos Communion: As a cleansed Klyntar, the Venom symbiote is able to hear the "voice" of the Cosmos telling it of people in need of assistance. 𖑡]
  • Humanoid Form: Since being cleansed, the symbiote has developed the ability to take on a humanoid form independently of being bonded to its host, for a maximum duration of twelve Earth hours. 𖏳] After coming into contact with Knull, this ability was augmented to enable it to disguise itself as a human. 𖐝]𖑢]
  • Proximity Tracking: Agent Venom can track others by leaving pieces of itself on others, seeking them out wherever they may go. 𖑣]
  • Self-Sustenance: The Venom Symbiote enables the host to survive anywhere in any hostile environment. Be it in the cold reaches of space, 𖏳] or fatally gaseous areas with relative ease. 𖑤] Flash could even impart this a hazardous element filtration system to others. 𖑕]
  • Morphomerge: One time while on mission Flash symbiotically bonded the Klyntar into a stripped and broken-down car in order to make it operational again. Said vehicle was not only greatly reinforced by its constituent matter but had the appearance, tentacles and biting maw normally reminiscent of its feral state. 𖑥]Tel-Kar was also able to use it to interface with his spaceship. 𖑦]

Physical Strength

The symbiote has enabled its hosts to lift up to 70 tons at regular size in the past, this was not their true limit as their strength increases with their variable muscle mass. With progressive mutation and the variable host shifts adding to Venom's power, a host's current strength level is unknown. [citation needed]


Sonic and Heat: The Symbiote is extremely sensitive to sonic and thermal attacks, making it vulnerable, although the degree of sensitivity has varied over time and the symbiote has built up a resistance. 𖑧]

Psychological Corruption: The Venom symbiote, like others of its kind, is susceptible to the negative emotions of its host - particularly rage and hatred. ⎛] ⎘] At its worst, the symbiote is a bloodthirsty predator that seeks to corrupt or outright control its hosts, compelling them to satiate its ravenous hunger. 𖑨] 𖑩] ⏜]

Knull: An ancient deity who created the symbiotes, Knull is able to mentally influence and dominate them, driving them insane with bloodlust and enslaving them to his will. [citation needed]

Accelerated Corruption and Degeneration: After the symbiote returned to Eddie Brock, its psychological corruption accelerated and was accompanied by physiological degeneration. Alchemax scientist Dr. Steven analyzed a piece of the symbiote and determined that Eddie's body had been rendered inhospitable to the symbiote through prolonged exposure to symbiote suppressant chemicals during his time with the FBI. 𖑪] Eddie's altered metabolism and the symbiote's corruption were cured when they were doused in Alchemax's Anti-Venom serum by Spider-Man. 𖐉]

Top 5 Ways Nature Has Inspired Technology

Engineers are in the business of solving problems. It's their job to find ways to achieve certain outcomes. The problem might involve finding a way to build a skyscraper that can withstand hurricane-force winds. Or it might be to discover a method to deliver a specific dosage of drugs to a single cell in the human body.

Engineers often look to nature to see if there's already a solution to the problem they currently face. Not only must they recognize the solution, but also be able to study, copy and enhance that solution so that we can take advantage of it. There's a special word for this approach: biomimetics. Ultimately, the engineer's creation mimics the structure or function of a biological entity.

The results can be awe-inspiring or something people routinely take for granted. But even the basic inventions wouldn't have been possible if engineers hadn't paid close attention to the way things work in nature. We'll take a look at five ways nature has inspired the technology we rely upon, listed in no particular order.

5: Developing Artificial Intelligence

Artificial intelligence is a term that has been thrown around for decades. In the past, computers were just powerful machines that could crunch enormous numbers -- they couldn't think for themselves. A computer could only follow explicit instructions.

Today, engineers and computer scientists are trying to make the leap from computation to thinking. They've met with some progress. In 2008, scientists used the BlueGene L supercomputer to simulate a mouse's brain. That might sound simple, but a brain -- even one belonging to a virtual mouse -- is incredibly complex. So complex, in fact, that the powerful computer could only run the simulation in bursts of 10 seconds [source: BBC News].

In 2009, Cornell researchers created a computer program that was able to derive the basic laws of motion by analyzing the movements of a pendulum. The program took a series of measurements and used a genetic algorithm to extrapolate the basic laws of physics.

In the future, we may see machines capable of solving complex engineering problems. We may even reach the point where computers design even more powerful machines. How's that for deep thought?

There are teams of engineers, computer scientists and doctors who are working on methods to cure cancer and other diseases on a cell-by-cell basis. One solution they're working on involves designing delivery technologies on the nanoscale. They're building medical nanoparticles -- objects that are smaller than 100 nanometers in diameter. A nanometer is one-billionth of a meter. In fact, the nanoscale is so small that it's impossible to view nanoparticles even with the aid of a light microscope.

The idea is elegant: Create a drug-delivery particle that can seek out a cancer cell, infiltrate it and deliver medication exactly where it needs to go. By targeting just the cancer cells, doctors hope to eliminate the disease while minimizing any side effects. Healthy cells would remain unaffected.

This is trickier than it sounds. But these teams have a natural model they can study to create nanoparticles: viruses. Viruses can measure only a few nanometers in length and are able to seek out specific kinds of cells somehow before replicating. Doctors hope to create nanoparticles that mimic this ability.

Since the dawn of time, man has searched for the ideal way to stick something to something else. In ancient times, this may have involved hammering a large spike through the hide of a mammoth to make the cave dwelling a little less drafty. These days, engineers look to plants with burrs or creatures like the gecko for inspiration.

Back in 1941, Swiss engineer Georges de Mestral was picking out burrs that had caught on his clothing and in his dog's fur. He placed a burr under a microscope and noticed that it had tiny barbs that allowed it to attach to passing creatures. The engineer came up with a brilliant plan -- create a material that used these tiny barbs as a fastening device. That material is what we now call Velcro [source: Stephens].

Then there's Gecko Tape, a material that uses nanoscopic hairs to cling to sheer surfaces. The hairs mimic the ones you'd find on the feet of geckos. One day, scientists might be able to create an entire suit using this material. That suit would allow the wearer to scale walls and perhaps even walk across ceilings. Before long, we may be able to put in a call to our friendly neighborhood Spider-man.

2: Navigating Autonomously

In the future, there will be robots. Whether they will cater to our every need or hunt us down in packs. It remains to be seen. Either way, one feature robots will need to achieve their true potential is autonomous navigation.

Most robots either require a pre-programmed route or simply react to the environment whenever they encounter an obstacle. Very few can find their way from one point to another on their own. Some engineers are trying to overcome this problem by studying ants.

The Cataglyphis is an ant found in the Sahara Desert. Unlike other ants, the Cataglyphis doesn't rely on pheromone trails to navigate through its environment. Scientists believe that the ants use a combination of visual piloting, path integration and systematic search [source: Möller et al.]. Engineers hope that by gaining a deeper understanding of how creatures like the Cataglyphis navigate, they can build robots with similar capabilities.

In 2000, Walt Disney Pictures released a new edit of "Fantasia." The updated film contained several new sequences, one of which featured a pod of humpback whales that take flight to the strains of "The Pines of Rome" by Ottorino Respighi. While we're not likely to see humpback whales take to the skies, the fantastical sequence presaged an actual scientific discovery.

In May 2004, a group of scientists and engineers published a scientific paper in the Physics of Fluids journal. The team had built models of the pectoral flippers on a humpback whale. On one model they included tubercles -- the bumps you'd find on an actual whale's flipper. On another model they used a smooth surface.

They tested both models in a wind tunnel at the U.S. Naval Academy. Their tests showed that the flipper with the tubercles saw an 8 percent improvement in lift. In addition, the flipper was less likely to experience stall at steep wind angles and created up to 32 percent less drag.

Could we soon see airplanes with bumpy wings? It's entirely possible. The team's findings suggest that nature has created an efficient device for moving through fluid environments. It might be foolish not to take advantage of these discoveries.

There are hundreds of other examples of how nature has guided technological development throughout human history. So the next time you need to solve a complex technical issue, you might just want to take a look in your own back yard first.