The Fossil Record
Sean D. Pitman M.D.
© May 2005


          The standard approach to looking at fossils in the geological column is to assume that lower is older. Since the geologic column represents millions of years of Earth's history, then obviously the fossils in each of the layers must be the same age as the layer in which they are found.  What is especially interesting is that the fossils do appear to show a progression from the most "simple" of organisms, such as single celled creatures like bacteria, to the most "complex" organisms, such as vertebrates, mammals, and of course humans. This evolutionary progression seems to be clearly demonstrated in that certain kinds of creatures in the upper layers are rarely if ever seen in lower layers. Many of the layers also show a certain specialization. Some layers contain mostly fish fossils while others contain land-dwelling creatures such as dinosaurs. Since each of these layers seems so specialized it is easy to conclude that one type of creature gave rise to the next type of creature over the course of whatever time it took to form the various layers between them.  Radiometric dating and many other techniques are used to support the idea that this transformation process took tens and hundreds of millions of years. 

          For most scientists all of this seems so obvious that it is difficult to question.  It goes against human nature to challenge long held ideas of truth.  However, science is suppose to do just that - challenge ideas.  Why?  Because often what seems obvious initially does not turn out to be true.  The scientific method is all about testing and retesting theories since no theory is ever proven by science.  The scientific method can only disprove theories or increase the power of previous predictions that have yet to be disproved, but it can never absolutely prove anything to be absolutely true.  Therefore, the best thing to do in science is to continually question and test previous hypothesis and theories to see if they continue to hold up under scrutiny.  So, let's take another look at the available evidence and see if any other possibilities present themselves.

          Surprisingly there are quite a few problems with the geologic column itself being a representation of millions of years of Earth's history.  Much of the evidence available seems to point more toward the rapid formation of much of the column.  Of course popular science disagrees stating that these layers represent millions of years of history and that the fossils they contain are likewise millions of years old.  However, there are just a few problems that might suggest another interpretation. 



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From Simple to Complex





What about the fact that the "simple" organisms are buried in the lower levels and the more "complicated" ones are buried in the higher levels? Doesn't this fact support the notion that simple organisms evolved into more and more complex organisms over time, with the more complex organisms buried and fossilized above the earlier and simpler life forms? Certainly this seems like a very logical assumption.  But, things just aren't that easy. There are a number of potential problems with this interpretation of the fossil record. 

For example, it is interesting to note that some general kinds of fossilized creatures are very generally found in the same relative vertical orientation, with respect to each other in the fossil record, that they would have naturally been found in during life. Single celled organisms make their first appearance in the lowest layers followed by multicelled ocean bottom-dwelling creatures like sponges and worms etc. Higher up come creatures like bony fishes, then land plants and animals, then birds and larger land animals.

Of course, this is a very general pattern and does not explain why certain creatures that lived on the bottoms of oceans, like trilobites, make their first appearance in the Cambrian (505-540 Ma) while other creatures that live on ocean bottoms, like crabs and lobsters, don't appear until the beginning of the Cretaceous (65-145 Ma).83  Why would creatures that would seem to share the same general environment while alive be so widely separated in the fossil record if they did indeed live at the same time and in pretty much the same location? If the geologic column truly represents a series of closely spaced catastrophic burial events instead of long ages of time, how can this feature be explained?  Certainly this is a difficult and rather mysterious problem for those, like myself, who might think to question the long age notion of the fossil record. 

However, this feature is also somewhat problematic for those who hold that the geologic column and fossil record developed over many hundreds of millions of years.  It seems like the fossil record is simply too neatly sorted.  Creatures suddenly appear without any prior record and then suddenly disappear without any subsequent record, only to reappear tens of millions of years later - alive and well (such as the history of the Coelacanth described in more detail below).  Many layers also have only a limited number of preserved creatures - far too limited an array to support a viable ecosystem.  For example, the fossils of some layers consist primarily of large meat eating dinosaurs. Yet, there simply aren't near the number of preserved creatures that could serve as prey for these very large carnivores.1  What on Earth did they live on for millions of years?  How did they get preserved in abundance in certain layers while other creatures did not? The same thing is true of millions of fossils of very large plant eating dinosaurs in places like the Morrison Formation.  This huge formation contains millions of preserved plant eating dinosaur bones but hardly any plant fossils.34,35  Could the difference in preservation between dinosaur bones and hard woody plant remains be that significant? - especially when large seems of coal and other finely preserved plant fossils are abundant elsewhere? And, what about pollen order?  Pollen appears fairly neatly sorted in the fossil record.  It seems, perhaps, that it is just too sorted.

There are so many other features of the geologic column and fossil record that seem just as difficult, if not more so, for the notion that very long periods of time are represented.  For example, it seems that many land animals, excluding birds and mammals, do not generally have their footprints located in the same layer in which their bodies are found, but in lower layers.56  Did the footprints evolve before they did?  The footprints of dinosaurs, for example, are generally located in lower levels than the actual fossilized bones of the dinosaurs.1,56,82  Why would this be?  What is there to explain this apparent sorting of body from footprint fossils? Leonard Brand and James Florence comment on this most interesting phenomenon:


If the geologic column represents sediments that have accumulated over many millions of years, and the fossils from each geologic period are the remains of animals living in successive time periods, it would be reasonable to expect that the stratigraphic patterns of footprint diversity should roughly parallel the patterns of equivalent body fossil diversity.56


Some have suggested various potential problems for this interpretation of Brand and Florence. However, these objections seem fairly well covered in the paper. I also discuss a few of these objections in detail in a Google Talk.Origins debate (Link).82

Some argue that such finely preserved trackways as are observed in the fossil record, such as the horseshoe crab fossil and trackway pictured here,57 were probably the result of the creature being trapped in an "anoxic lagoon".  But how are such crisp footprints and such a well-preserved body going to be preserved at the milky bottom of some anoxic lagoon?  Where are such conditions described preserving such fine fossils today?  Also, scavengers are still active even in highly anoxic conditions.  What made it possible for such delicate footprints and bodies of such creatures to be preserved in such fine detail - avoiding all hints of bioturbation? 

Bioturbation is an extremely effective way of destroying layering in sedimentary rocks by mixing up the sediment and homogenizing it. It is easy to find modern-day examples of this. Hurricane Carla laid down a distinctive layer of sediment off the coast of central Texas in 1961. About twenty years later, geologists returned to find out what had happened to this layer. Most of the layer had been destroyed by living creatures burrowing into it and disturbing it; and where the layer could still be found it was almost unrecognizable.

In the light of such modern day findings, it is very difficult to imagine how such layering of sediment found throughout the geologic column and such crisp lines between these layers could have been kept in such pristine condition for not only tens or hundreds of years, but hundreds of thousands and even millions upon millions of years of time. It is even more difficult for me to imagine how such finely detailed fossils and trace fossils could be preserved. 

Rather, it seems to me that the fossil presented here, with its trackway, was preserved by rather rapid and deep burial by sedimentary layering.  The horseshoe crab survived the first periods of layering, making its trackway on a newly deposited surface, only to be overcome quite suddenly by a subsequent depositional events which were so rapid that the horseshoe crab, which was probably very good at digging, was trapped with such pressure that it could not escape.  Its body and fine trackways were also preserved because of the sheer deepness of the burial - which prevented subsequent disturbance by bioturbation. 

To suggest that such trackways, in particular, could be preserved in the bottom of some anoxic lagoon just doesn't make nearly as much sense to me.  However, if someone can show me a real life example, I'd be more open to such potential explanations. 

Also, what is usually overlooked is that fact that there is no such animal as a "simple" animal.  All living things are extraordinarily complex. The "simplest" one celled organism, such as a bacterium, is just a complicated as a single cell that exists in the body of a human being - using just as many genetic functions at any one time.  A rat is also no less complex than a human as far as the information needed to build a rat.  In fact, out of 35,000 to 40,000 genes that the human genome contains, the rat is only about 500 genes different.9  Certain plant species also require a similar amount of functional genetic material (i.e., genes).  

Consider also the fact that many mainstream scientists believe that all the main forms (or phyla) of animal life, save perhaps one, that exist in the world today were all present in the Cambrian - said to be over 500 million years old. Of course, not all have actually been found in the Cambrian layer since many have only soft body parts that are difficult to preserve or fossilize. Still, based on phylogenic analysis nearly all animal phyla that exist today are believed by most scientists to have arisen during or just before the Cambrian period over the course of a few tens of million years.  This rather sudden appearance, relatively speaking, of nearly all animal phyla during the Cambrian period is referred to as the 'Cambrian Explosion'. After this period essentially no new phyla are thought to have evolved over the course of hundreds of millions of years. Compared with the 35 or so animal phyla that still exist today, some people estimate that the Cambrian explosion may have generated as many as 100 different phyla. This prompted those such as Roger Lewin to ask, "Why, in subsequent periods of great evolutionary activity when countless species, genera, and families arose, have there been no new animal body plans produced, no new phyla?" 78  (Back to Top)





Oriented Dinosaur Bones




As far as the fossilized bones of large animals, such as the dinosaurs and large mammals, they are also generally oriented in the same direction for any given layer, and this is true the world over.  Did these animals position themselves in the same direction as they died?  This does not really sound too likely.   Even the legs and tails of these animals are oriented in the same direction for a given sedimentary layer.  How does this happen?  If you think this is strange, consider also that huge masses of large bones are found matted together in places like Bighorn Wyoming.  Did these animals choose to die in the same location and in the same general orientation? Some have argued that the bones from Bighorn, Wyoming (pictured to the right) are not really oriented since they obviously pictured as pointing in different directions. However, water flow orients long thin objects in two ways - perpendicular and parallel relative to the flow of the water.  There are many places where literally thousands of fossilized skeletons can be found all mixed up together in mass burial.  In many of these places the bones are severely damaged, fractured, and mangled - yet oriented.  It is all quite interesting as well as very difficult for today's popular scientist to easily explain, if at all, without using a catastrophic flood model.1  

Consider also the Jurassic Morrison Formation (famous for its dinosaur fossils). It covers over 1,000,000 square kilometers - being spread from Canada to Texas.  It has been suggested that it was distributed by widespread flowing water. The fossils found within it, millions upon millions of them, are generally oriented with respect to flow - confirmed by GPS mapping (Arthur Chadwick). However, ancient channels of major rivers that would help distribute the sediments over such a wide area have not been found. Jack Horner noted the same thing, orientation with respect to flow, in the Montana deposits containing tens of thousands of dinosaurs.58  (Back to Top)





The Exquisite Preservation of Large Fossils




The bodies of some very large fossils, such as dinosaurs or whales are occasionally very well preserved. Of course, the geologic layers that contain their fossilized remains are supposed to represent thousands or even millions of years of Earth's history.  However, the bodies of these large creatures take up a fair percentage of the thickness of some of these layers.  This might just pose a bit of a problem for the standard way of interpreting these fossils and the layers of sediment in which they are found.  Obviously, If sedimentation slowly buried them over the course of very long periods of time, their bodies would not have survived.  For fossilization to occur, burial or some other form of preservation must be fairly rapid in order to protect the remains from significant scavenging and/or decay.  

With this in mind, it seems like the entire layer that such fossils are found in could not possibly have been formed over vast periods of time.  Rather, it seems like such fossils speak of a relatively sudden burial event or events, or some sort of rapid process of fossilization without burial - sometimes on massively catastrophic proportions covering hundreds of thousands or even millions of square kilometers.  The very high degree of preservation of fine details of some of these fossils give evidence of a rather sudden burial or preservation process, and not of a natural death with slow burial or preservation giving time for decay.  Many fossils show evidence of surprise or being startled, such as elevated dorsal fin spines or tightly close clams, or a brief struggle before death - like they were suddenly buried or rapidly preserved by other processes (like sudden crystallization) extremely quickly.  Some fossils are found with food still in the mouth of the victim (in mid chew).  Others have been found suddenly frozen in the process of giving birth and others have been found with fine soft tissue detail down to the cellular level (still turgid gills of fish preserved in the Santana Formation - indicating complete fossilization in less than 1 hour).

It is my personal opinion that such fossil evidence favors a catastrophic interpretation for much of the geologic column.  Interestingly, this notion isn't as "fringe" as it used to be just a few decades ago. Mainstream scientists are starting to lean more and more toward catastrophism. This is quite interesting because, for a very long time, mainstream scientists where "uniformitarian" in their thinking.  


"From around 1850 to 1980, most geologists endorsed uniformitarianism ("The present is the key to the past") and gradualism (geologic change occurs slowly over long periods of time) and rejected the idea that cataclysmic events such as earthquakes and volcanic eruptions played any significant role in the formation of the Earth's surface. In part, the geologists' rejection was fostered by their impression that the catastrophists of the nineteenth century believed that God was directly involved in determining the history of Earth. Catastrophism of the nineteenth and early twentieth centuries was closely tied to religion and catastrophic origins were considered miraculous rather than natural events."79


The uniformitarian notion of slow deposition over millions of years of time is no longer accepted by scientists.  It is now believed that various catastrophes, large and small and sometimes worldwide, played a key role in the Earth's history and are recorded in the geologic column. In this regard, consider the following comments from David, M. Raup of the Chicago Field Museum of Natural History:


"A great deal has changed, however, and contemporary geologists and paleontologists now generally accept catastrophe as a 'way of life' although they may avoid the word catastrophe... The periods of relative quiet contribute only a small part of the record. The days are almost gone when a geologist looks at such a sequence, measures its thickness, estimates the total amount of elapsed time, and then divides one by the other to compute the rate of deposition in centimeters per thousand years. The nineteenth century idea of uniformitarianism and gradualism still exist in popular treatments of geology, in some museum exhibits, and in lower level can hardly blame the creationists for having the idea that the conventional wisdom in geology is still a noncatastrophic one."80


Also, consider the following comments by Robert H. Dott given during a Presidential Address To Society of Economic
Paleontologists & Mineralogists:


"I hope I have convinced you that the sedimentary record is largely a record of episodic events rather than being uniformly continuous. My message is that episodicity is the rule, not the exception. . . We need to shed those lingering subconscious constraints of old uniformitarian thinking."81


It seems then that catastrophism is only recently being accepted by more mainstream scientists.  It seems also that significant portions of many different sedimentary layers within the geologic column are now thought, even by popular science, to have been the result of rather sudden catastrophic deposition - with the bulk of time passing in between these episodes of catastrophe. Although the notion that the geologic column might not actually represent millions of years of time is far from mainstream, mainstream thinking is actually drifting back toward a position that can actually begin to consider that catastrophes and episodicity are "the rule, not the exception." This notion is something fairly new in mainstream thinking. Even today there is strong resistance of any notion that comes to close to suggesting catastrophes of "Biblical proportions" - perhaps due to the engrained bias against literal Biblical interpretations that suggest such things as a worldwide flood.  Consider the story of J Harlen Bretz as a fascinating example of this sort of resistance. 

In this line, the fairly recent discoveries of fossil whales (Miocene/Pliocene) in western Peru are quite interesting. Leonard Brand (Ph.D. in Paleobiology from Cornell) comments, "In our survey of the area, we found the fossil remains of more than 100 whales in an area of less than two square kilometers… What was even more exciting was the well-preserved nature of the fossil remains. . .  Typically, when a whale dies at sea, the carcass falls to the bottom and becomes the source of a rich ecosystem. Many species of sea life benefit from the decaying remains at each stage of the process. Within four to six months, the whale carcass has been mostly stripped down to the bones. At that point, other species of organisms burrow both into the bones and the surrounding sediment. Within a year or two, the whale bones show much evidence of these burrowing animals."52 

So, how did the whales in western Peru meet their end? "These whales were incredibly well-preserved," Brand observes, "suggesting that they were covered quickly." Brand found that the whale remains were blanketed by a thick layer of diatomite (silica remains of diatoms). These tiny creatures, known collectively as plankton together with dinoflagellates, are part of the food source for whales. In modern times, diatomite normally accumulates on the sea bottom at a rate of a few centimeters per thousand years. "We also found beautifully preserved baleen," he adds. Baleen refers to the filtering feather-like structures in the whale's mouth that are used to strain out food (plankton) from the water. "Whales feed by gulping in water and forcing it out through the baleen, trapping the tiny plankton." Baleen is actually more akin to the human fingernail or toenail in its structure. "The well-preserved baleen supports the theory of a quick burial to an even greater extent".52 

But why did the whales die in the first place? "There is more and more evidence that red tides--blooms of diatoms and dinoflagellates--produce toxins which can kill large animals and fish," he says.52 These massive blooms were so large that they not only killed the whales, but buried them in thick layers before any significant decay could set in.

Another very startling finding that demonstrates the sudden/catastrophic burial of very large creatures is a 1971 finding in Southern Mongolia of a perfectly articulated Protoceratops and a Velociraptor frozen in a life and death struggle with each other.  Obviously these two creatures were buried suddenly by a huge catastrophe of magnificent proportions.  The dinosaurs didn’t even have time to fall over. 51

Many dolphin-like ichthyosaur fossils also show evidence of rapid burial - such as those found clustered together at places like the Berlin-Ichthyosaur State Park in Nevada.  Some ichthyosaurs that show evidence of rapid burial are buried with certain other ichthyosaurs that show evidence of rather brief exposure and/or scavenging in the same region.  Isn’t it strange that creatures showing evidence of some exposure are buried closely with others that show evidence of very rapid burial?  According to scientists studying these fossils, "It is not yet certain how these large creatures died and were buried together in such a small area."  Also, at least in the Nevada location, "the skeletons are generally oriented along a north-south axis, suggesting that currents or tides played some part in deciding their final resting place."

Other evidences of rapid ichthyosaur burial include some specimens that were suddenly buried in the middle of giving birth!  A number of these partial birth fossils have been found in Germany showing baby ichthyosaurs frozen half way out of their mother’s birth canals (see figure below).

Consider also the large size of adult ichthyosaurs.  In order to preserve such large specimens, in such well-preserved condition, fairly rapid burial is required.  These are all indications of some sort of sudden event that resulted in the relatively simultaneous deaths of many ichthyosaurs as well as their relatively rapid burial.  

Some prolonged exposure of such large creatures as ichthyosaurs is only to be expected, but the fact that their fossil remains were preserved in an articulated fashion, often with evidence of soft tissue detail, speaks in favor of a fairly rapid burial process with little chance for significant decay and/or scavenging.   Also, many creatures may die at the same time and then be buried rapidly at slightly different times by repeated waves of sediment deposition.53 (Back to Top)







The Living Fossils






The coelacanths are fish having a flexible oil-filled type of back bone that gives them their name. In place of the bony vertebral column of most adult fishes, coelacanths have a large, thick tube of cartilage, called the 'notochord'. In the early development of most fishes, the notochord of the embryo or larva is gradually replaced by the bony (or calcificed) centra of the vertebral column.  But in coelacanths, lungfishes and some types of sharks, the transformation of notochord into a segmented bony (or calcified) vertebral column does not take place.  In coelacanths, the hollow notochord is filled with oil and provides a strong, yet flexible support for the spinal cord. 41  

Coelacanths are thought to be very ancient fish who lived before, during, and after the time of the dinosaurs.  However, like the dinosaurs, the coelacanths vanished from the fossil record (some 80 million years ago).  However, before they seemingly went extinct they lived prosperously for nearly 400 million years.  They are in fact thought to be the ancestors to the first vertebrates to step out of the seas and walk on dry land some 350 million years ago.  Because of this belief that coelacanths are an important evolutionary link between sea and land dwelling vertebrates, special significance has been given to their place in the fossil record.  In fact, it was long thought that the fossil record was the only place where coelacanths would ever be found.  This seemed to be true until 1938 when living coelacanths were found alive and well off the coast of South Africa living at a depth of around 120 to 250 meters. 41  Since then, other colonies of coelacanths have been found in various areas such the coast of Madagascar, Sulawesi (Indonesian Archipelago), Mozambique, and Comoran.  

The initial discovery of living coelacanths came as quite a shock to the scientific community.  To find a "living fossil" after it had vanished from the fossil record for some 80 million years was quite a stunning revelation.  How could this be explained?  How could a creature be preserved/fossilized over and over again during the course of 300+ million years and then vanish for some 80 million years only to reappear, alive and well, in modern oceans?

Well, there are several explanations commonly given to explain such a phenomenon.  Perhaps one of the more popular explanations is that the modern coelacanth is not the same creature as those coelacanths found in the fossil record.  In fact, the differences are thought to be so significant that modern coelacanths have not only been classed in a different species category, but in a different genus group as well.  The classification of the modern coelacanth Latimeria chalumnae verses the very similar fossil coelacanth Macropoma lewesiensis, goes as follows:



Coelacanth Classification


Kingdom: Anamilia vs. Anamilia

Phylum: Chordata vs. Chordata

Class: Osteichthyes vs. Osteichthyes (bony fishes)

Order: Coelacanthini vs. Coelacanthini

Family: Sarcopterygii vs. Sarcopterygii

Genus: Latimeria vs. Macropoma

Species: chalumnae vs. lewesiensis






Many "emphasize" the point that, "The living coelacanth is not a living fossil in the very strict sense that members of the species L. chaumnae itself have never been found as a fossil.  In fact, no other species assignable to the Genus Latimeria has been found as a fossil either.  Latimeria and the Cretaceous fossil Genus Macropoma are quite closely related, and we could possibly include them in the same family.  Beyond that, all fossil coelacanths belong to the order Coelacanthini." 38,40

The problem with this argument, as discussed in some detail above, is that phylogenic classification schemes are quite subjective.  A comparison of the modern coelacanth with those found in the fossil record really does not necessitate their being any more different from various breeds of dogs who are all members of not only the same genus and family groups, but the same species group as well.  Even so, some do argue that, "A person can see substantial differences in the fins, tail, lobe fin, and drastic changes in the structure of the head." 40  However, it seems to me that this is an over emphasis when such differences are no more drastic than the differences that are seen within species groups (ie: bulldog vs. German Shepherd).  It is true that the picture comparisons do show some obvious differences, but these do not seem to be as striking as many seem to suggest.  The lobe fins themselves are almost identical.  The tails are also practically identical excepting for comparisons of the "supplementary tail fin."  The problem here is that the supplementary tail fin was left out of the drawing of the fossil coelacanth, Macropoma lewesiensis (as were the fin bones).  This is because, "Details of the fossil's supplementary tail fin are insufficiently known to allow restoration" (The same can be said for the fin bones).  This leaves, basically, the "drastic changes in the structure of the head" as the only real possible difference between the two coelacanths. 

It appears that the two heads are in fact very similar as far as the number, relative position, and general shape of the bones in the two creatures.  It seems like the main differences can be found in the relative size of the various bones or bone proportions.  These differences give Macropoma a longer and more pointed snout than is found in Latimeria as well as a bit of an overbite.

Based on these rather minor differences these two creatures are classed, not just as different species, but as members of different genus groups.  Are these differences really greater than the range of comparable differences found within the range of other species, such as domestic dogs or even modern humans?  Consider, for example, the differences between a German Shepherd and a bulldog.  The German Shepherd has a long, narrow snout with an overbite, while a bulldog has a short, flat snout with an underbite.  These differences might even be called "drastic."  If the bulldog phenotype where found only in the fossil record and the German Shepherd were living today, would they be classed in the same species or even genus groups when compared side-by-side?  I doubt it…

In this light, the statement that "No other species assignable to the Genus Latimeria has been found as a fossil", seems to me to be a bit misleading.  In fact, Peter Forey, in his book, "History of the Coelacanth Fishes", comments that the skeleton of Macropoma lewesiensis is "virtually identical to that of the coelacanths caught off the Sodwana Bay, Latimeria chalumnae, and differs little from the skeleton of most Devonian coelacanths." 39,40   The problem is that there does in fact seem to be a tendency to place very similar fossils in different categories based primarily on the fact that they obviously lived so far apart in time that they can not possibly be members of the same species.  This practice seems to be the rule rather than the exception.  So, to say that the L. chaumnae species has never been found in the fossil record seems to me to be stretching it a bit since this species classification is based on very minor morphologic differences that are clearly within the range of intra-species variation. 

So why then, did the coelacanth disappear from the fossil record for 80 million years?  Other arguments are that only those coelacanths that lived in more shallow water environments died out while the deep water variety managed to survive.  The deep water environment occupied by many modern coelacanths is thought to be very poorly conducive to both fossilization and discovery.  Other coelacanths, such as those colonies that have been found more recently living off the coast of the Comoro Islands, live in shallower waters but over steep slopes of these volcanic islands.  Some scientists, such as Hans Fricke (a coelacanth specialist) suggest that, "these slopes are too steep to hold sediments that could rapidly cover a dead fish and thus begin the fossilization process."  The steep slopes and underwater caves that form the habitat for the modern coelacanth simply do not allow for the fairly rapid sedimentation and burial needed for fossilization to occur.  Also, deep water prevents scientists from exploration and discovery even if such fossilization did occur.  Additionally it is thought that continental subduction might have destroyed such deep sea fossils as well.40

These arguments are all well and good except for one thing.  If coelacanths were so successful for hundreds of millions of years in areas quite conducive to successful fossilization, then why, when they died out of such areas, did they not evolve back into these niches over the course of time?  Why did these niches that supported coelacanths so successfully over the course of hundreds of millions of years never become repopulated over the course of 80 million years by populations of coelacanths living elsewhere?  Really, 80 million years is a fair amount of time.  One might think that surviving populations of deep-sea coelacanths might fluctuate in size.  They might even "evolve" the ability to populate rivers and lakes again.  Is it not strange that in 80 million years, the surviving populations of coelacanths never found opportunity to evolve back the ability to live in their former habitats… where they were previously so successful?  After all, it seems like a much shorter step to go from a deep sea environment to a shallow water environment than to go from swimming to walking around on land.  If the coelacanths gave rise to land dwelling creatures in a few million years, then why was it so difficult for them to win back their former water-based environments? (Back to Top)




Shale Bed Trace Fossils



Shale beds, such as the Yesnaby Sea Stacks and the Dougherty Gap Outcrop pictured here, are formations that are often composed of alternating layers of shale and sandstone.  The various layers range from one or two millimeters to several meters in thickness.  The layers of shale where once layers of clay that have become compressed and hardened into shale.  It is generally thought that such layers were formed over several million years by the repetitive deposits of shallow lakes, swamps, and rivers.  With the changing sea-levels due to glacial activity, the resulting cyclical drowning of these areas is thought to have resulted in the cyclical deposition of clays, silts and sands over fairly significant spans of time.  Some of these beds are in fact quite thick.  For example, the Haymond Beds average around 1,300 meters in thickness and contain thousands of layers of shale and sandstone.  However, what is especially interesting about many of these layered beds is that they contain "trace fossils". 59  

Trace fossils are the evident remains of tracks or imprints that some creature left behind even though the actual body is not there.  For example, when the shale was first formed as an organically rich clay, many burrowing creatures lived in it, filtering it for nutrients.  As they moved through it, they left trails behind.  When this clay was buried by turbiditic sand flows, the sand filled in these tunnels, trails and other impressions.  As the sand solidified, the casts of these tunnels and other markings were preserved on the underside of the sandy layer.  Since this underside of a layer is called the "sole", the preserved impressions in the clay are called "sole casts."

Many argue that these layers must have been formed over long periods of time because colonies of such burrowing creatures take time to colonize each layer of clay as it forms.  The burrows themselves take a fair amount of time to create.  Glenn Morton, a vocal geologist, comments that, "These burrows are horizontal and the animals don't seem to be digging out.  They are digging through the sediment.  And there are thousands of layers of sediment with the burrows on them." 61  Morton actually suggests that when each sandy turbidite covered a layer of clay that the burrowing creatures didn't burrow out, but died when the sandy layer covered the layer of clay.  He says, "We know that the burrowers who were buried did not survive.  If they had, they would have had to dig up through the sand to escape their entombment.  There are no burrowers going up through the sand.  And, if there had been these burrows, there should be little circular piles of sand with a central crater pocking the entire upper surface of the sand.  We don't see these." 59   

Glenn Morton is not the only one who thinks this way.  This is in fact the prevailing paradigm about how these layers must have formed.  However, there may be an even more reasonable explanation.  If these layers were in fact formed over long periods of time where each individual layer took at least a few years to form, it seems like tunneling organisms would mess up the layers.  Look at the pictures presented here.  Most of these layers are very thin, averaging only a few centimeters in thickness.  And yet, they are extremely crisp and distinct from the layers above and below.  Burrowers living in lake or ocean bottoms or swampy areas, burrow all around and cause mixing of the sediments.  Such mixing is known as "bioturbation."  However, even the thinnest sandstone units fail to show any obvious signs of bioturbation, blurring of bedding contacts, or internal bedding features. Rather they appear as homogenized small-grained sandstones clearly demarcated from the overlying and underlying layers of shale.  Further evidence suggesting a more rapid formation of the layers comes from work done by Kuenen in 1967.  Kuenen documented the differences in sand textures between interdistributary bay deposits and turbidite deposits. Using his work as a reference the sandstone units found at Dougherty Gap best correlate to turbidite emplacement based on both lithology and bioturbation.  Also, the work of Coleman and Prior gives even more support for this idea.  In 1980 they presented photographs of cores taken from a modern interdistributary bay which in no way resemble the stratigraphy or sedimentation found exposed at the Dougherty Gap site. 60 

Another interesting finding is that these layers get thicker as one move up the various outcrops.  This finding is a common characteristic of rapid turbidite deposition and is "believed to reflect the progradation of submarine fan lobes." 60  In any case, this finding is not consistent with a slow cyclic deposition over vast spans of time.

The sand in the sand layers is also, "well sorted" meaning that it probably was not deposited slowly. "Good sorting is particularly significant because the sands are found in an environment where, unless deposition is very fast, one would expect silt and clay to be contributed..." 60

Also, almost every sandstone layer exhibits some degree of sole casts on its bottom surface as well as ripple marks on its top surface.  The upper surfaces of all of the sandstone layers, no matter how thick or thin, were found to contain "asymmetric, linguoid ripples"  According to Sheehan "... these structures formed in response to unidirectional currents which occurred either contemporaneously (at the same time) or penecontemporaneously (immediately following) with sediment deposition." 60

Given all of these findings, what theory makes more sense?  Were these layers deposited slowly where each layer was created over the course of tens, hundreds or even thousands of years, or were these layers formed rapidly by successive turbiditic flows in a highly silted watery environment?  Is it reasonable for those such as Glenn Morton to suggest that burrowing creatures give evidence of a slow formation?  What about the argument that such burrowing creatures must have been killed by each sandy turbidite so that a new colony of burrowing creatures would have had to take over the next layer of clay?  This argument makes no sense at all. Since when does a few centimeters of sand kill any burrowing creature?  This argument sounds almost silly, especially if one has ever tried to bury such creatures under sand at the beach.  They simply dig out in short order.  But, what about the fact that no evidence of "escape burrows" with "little circular piles of sand with a central crater pocking the entire upper surface of the sand" can be found?  No one who considered that the tops of each sand layer shows current ripples would ask such a question because the watery current would surely have removed any such piles of sand in short order as soon as they were made. With each new sandy turbidite the burrowers would simply burrow up through the sand to populate the newly forming layer of organically rich material as it rapidly formed over the turbiditic sand flow in a heavily silted environment. More and more layers would have formed in rapid succession leaving no time for the bioturbation of lower layers. 60

We are left then with the curious findings of thin crisp alternating layers of shale and sandstone showing no evidence of bioturbation between layers and increasing layer thickness as one moves up these formations.  This sort of layering is only consistent with rapid formation and cannot be explained by the prevailing paradigm where millions of years are required to produce such shale bed formations. (Back to Top)



The Coconino Sand Dune Trace Fossils


However, what about those ancient desert sand dune layers in the Grand Canyon?  The popular science of today declares that the Coconino Sandstone layer (third from the top) used to be an ancient desert formed over eons of time.  It is interesting that most of the layers in the Grand Canyon are felt to have formed under water.  However, the Coconino Sandstone layer is felt to be an exception to this rule.  This theory would mean that a layer of water-deposited mud (the Hermit Shale) was followed by a layer of wind-deposited desert sand over the course of between 5 and 10 million years, and then the area was again covered by water and the Kaibab limestone was deposited.  

The Coconino Sandstone layer is quite interesting indeed.  It averages 96 meters in thickness (315ft.) and covers an area of 200,000 sq. miles to include most of northern Arizona from the Magollon Rim, northward to the Utah border.  It is up to 1,000 feet thick at its southern edge and thins to a few feet at its northern boundary.  The total volume of sand is estimates to be approximately 10,000 cubic miles.62 The sand grains themselves are fine grained, well rounded and sorted, and composed almost entirely of quartz with no silt or mud contamination, just like most desert sand is.  Also, just like in modern deserts, the Coconino Sandstone has inclined “cross bedding” in it.  Cross bedding in sand dunes are areas were sand from one dune are covered by sand from another dune in a different orientation (different incline).  The Coconino Sandstone is filled with these cross beds just like desert dunes frozen in time.63  The sand grains themselves show microscopic features of long exposure in dry “desert” conditions.  These features include “frosting” and “pitting” on the surface of the individual grains of sand.  This similarity between Coconino Sandstone and modern desert sand has strengthened the belief that an ancient desert formed the Coconino Sandstone.64  Then comes the clenching argument:  All throughout the sandstone are preserved footprints of vertebrates such lizards or other similar reptilian or amphibian creatures, as well as less common worm, spider, and arthropod trails - and even some burrows.  The vertebrate tracks have been referred to as "amphibians and/or as reptiles," but from the structure of the tracks the majority of them are most easily interpreted as amphibians however strange it might be to have a majority population of amphibians living happily in a desert environment.  This is generally explained by suggesting that the desert sands bordered the ocean or a seaside area.  The footprints are located on the preserved surfaces of the dunes and are believed to have been covered by the shifting dune sand and thus preserved for all time.65  No other fossils have been found in the Coconino Sandstone to include evidence of any plant life (which seems strange since animals and plants usually go together - even in a desert).  But, given all of these facts, it seems obvious to many that the Coconino Sandstone is in fact a preservation of a very large and ancient desert.  

The popularity of the desert origin for the Coconino Sandstone began with the work of McKee in the early 1930s.74  McKee initially focused on the physical qualities of the sandstone to support his conclusions that the dunes had been wind and not water deposited.  Later he studied the footprints and concluded that they were most likely formed on dry sand.75,76  However, according to Leonard Brand, "Sedimentary features that were formerly thought to be diagnostic of eolian deposits are now known to be non-diagnostic. Stanley et al. (1971) pointed out that "grain frosting is no longer considered a criterion of wind transport," grain size distribution statistics have been ambiguous (for the Navajo), and "it can no longer be assumed a priori that large festoon cross strata prove an eolian dune origin for the Navajo or any similar sandstone because of the essential identity of form and scale of modern submarine dunes or sand waves, as documented during the past decade" (e.g., see d'Anglejan 1971; Harvey 1966; Jordan 1962; and Terwindt 1971)."72  

  But what about the fact that the Coconino Sandstone has preserved crisp footprints in delicate detail?  Well, does such detailed trackway preservation happen in dry desert sand?  When a lizard walks or runs over dry sand, what happens?  Footprint impressions are made, but nothing near the detail and crispness that has been preserved in the Coconino Sandstone is produced.  Now, consider the likelihood that shifting sand will preserve very small and delicate footprints made in dry sand.  This seems a bit hard to imagine.  In fact, laboratory experiments in real time have shown that the level of detail found in the Coconino Sandstone is best explained by the formation of the tracts underwater or on sand that has been wetted and left standing overnight.  According to Brand's experiments the damp sand trackways that did not stand overnight always had definite foot impressions but the toe marks were rarely seen.  The dampened surface formed a crust of sand that broke apart into many small pieces when the animals walked over it.  Sometimes these pieces of crusted sand would be pushed up into a pile at the back of the footprint or be scattered on around beside the footprint on the surface of the sand.  However, if the dampness of the surface of the sand was thick enough so that it would not break up with the weight of the animal, the sand would become rather hard and resistant to track formation.  The only tracks produced on this kind of wetted sand were a series of small dimples left by the toes.   The fossilized Coconino Sandstone tracks did not match the dry or dampened sand tracks produced in the laboratory by Brand in several ways.  The dry and damp sand tracks rarely preserved toe marks or other details, while the fossilized tracks usually did preserve toe marks.  Dry sand tracks also had large ridges of sand behind them which often flowed back into the previous footprint.  Again, the fossil footprints do not have these ridges nor were jumbled pieces of crusted sand observed to be scattered around the fossilized tracks.  The proportions of the tracks were also different.  Brand noted that the dry sand tracks were longer than they were wide, but the fossilized tracks were short in relative to their width.  The tracks made in the damp sand were simply too indistinct to allow adequate measurements.

Brand also did experiments in which the slope of the sand rose above the water line.  As the animals walked up out of the water their tracks changed as they went higher and higher from the waterline.  Footprints close to the water level were poorly defined while those a little higher were crisp and clear as far as toe marks and sole impressions.  However, as the animal progressed even higher to the more firm sand, the tracks became fainter and fainter until only toe mark dimples could be discerned.  This transition effect from well-defined prints to vague toe marks or scratches is not seen in the Coconino Sandstone.  

So why did Mckee believe that the tracks found in the Coconino Sandstone were made on dry desert sand?  Mckee was heavily influenced in the formation of his desert theory by the influence of a paleontologist by the name of Peabody who told McKee that salamanders do not generally make tracks underwater but prefer to swim from place to place instead of walk.  And, even when they do walk, they are partially buoyed up by the water so that their tracks are vague at best. McKee seemed to indicate that he had experimentally confirmed these suggestions made by Peabody.  Thus, McKee (1947) concluded that the fossil tracks preserved in the Coconino Sandstone were most similar to the dry sand trackways produced in his own experiments because only in dry sand were any definite prints of individual feet formed.  What is strange though is that there is no documentation of how extensive McKee's observations were as far as observing salamanders and their swimming or walking habits while under water.  

Brand, on the other hand, documents that all five species in his study walked on the bottom sands underwater more than they swam from place to place through the water  as long as they had a sandbar or some place in the testing tank where they could rest.  Brand noted that this behavior is also observed in the field.  When walking along the sand underwater all five species selected by Brand produced distinct footprints with toe marks and occasional sole impressions all along their trackways.  Some of the prints also had ridges of sand pushed up behind them, but these ridges never extended back into the previous print.  Brand concluded that, "The underwater tracks were most similar to the fossil tracks. Underwater trackways had toe marks as often as the fossil tracks, and they were uniform in appearance the full length of the sand slope, as the fossil tracks are. Also, the proportions of the fossil tracks were most similar to that of the underwater tracks." 72  However, Brand did leave open the possibility that such trackways could have been formed on a special type of wetted sand that had been wetted for several hours (overnight in his experiments).  Based on this evidence many argue that the desert was wetted on occasion by light mists, dew, or a heavy fog.  This allowed the various creatures living in this ancient desert to make their crisp trackways, which were subsequently covered by dry sand and preserved.  Other dry-land features, such as raindrop impressions, crisp and steep leeward dune fracture faces and cracks in the sand, and the preservation of spider trackways are often cited as evidence in support of this dry-land formation hypothesis in opposition to Brand's underwater hypothesis. This dry land hypothesis quite reasonable in many respects that seem to require open air exposure, but there are still a few other very puzzling features that do not seem so consistent with a true desert-like environment or dune formation.

 What is rarely mentioned in the literature is that the vast majority of the Coconino trackways all head uphill.66  Evidently the lizards/amphibians, arthropods, spiders and other creatures living in ancient deserts did not like going downhill much at all.  Also, trackways often start and stop suddenly without evidence of sand-shift or disturbance - like the creature suddenly vanished into thin air (or swam off in the water).66,67,68 

McKee attempted to explain the relative absence of downhill trackways by suggesting that the animals tended to "slide" downhill, thus obliterating their own tracks in the sliding sand. One might wonder why the animals would slide downhill when they were doing do fine going uphill without the sliding problem.  Those who have ever visited areas with desert sand dunes will find that trackways on such sand dunes go every which way.  Also, one would expect that wetted sand would be much more cohesive than dry sand and preserve tracks just as crisply no matter which direction the creatures were heading.  And, just in case there was any doubt, Brand performed a few more experiments.  Brand actually went to the trouble of inducing his experimental animals to walk both downhill as well as uphill.  On underwater sand, wet sand, and damp sand, almost all downhill trails produced easily recognizable trackways.  On dry sand, the trackways of salamanders were less well defined, but still relatively well preserved, while that of lizards were still quite distinct (both walking or running slowly).  Only when running very fast did their tracks become unrecognizable.  Thus, the almost complete absence of downhill tracks in the Coconino Sandstone layers seems to remain a mystery if they are truly desert formations.  It almost seems as though the creatures were trying to escape something, like rise water levels, and that is why they were all generally going uphill?

Brand also noted one other unusual aspect of some of the Coconino trackways. On occasion, there would be trackways that would head directly across a given slope at one angle or another, but the toe marks of both the back and front feet would be pointed up the slope.  It seems unlikely that the animals that made these trackways would have walked sideways for such distances.  Some have argued that desert lizards sometimes walk sideways in order to angle themselves to reduce the absorption of heat radiated from the scorching desert sand.  The problem with this argument is that the sand was wet and therefore relatively cool - certainly not scorching hot.  Others have suggested that a strong wind blew the animals sideways.  This idea requires a very strong wind indeed to blow a relatively low profile lizard or salamander sideways in an even pattern for significant distances. Brand suggests that the more likely explanation is that these animals were walking in an underwater current, which seems at least plausible.

Also, the architecture of the Coconino sand dunes is not like that of modern sand dunes in modern deserts. The Coconino sand dunes have an average slope angle of 25° while the average slope angle of modern desert dunes is 30-34° (the “resting” angle of dry sand).69 Sand dunes formed by underwater currents do not have as high an average slope angle as desert dunes and do not have “avalanche” faces as commonly as deserts dunes do.  Some crisp avalanche faces are found in the Coconino Sandstone dunes suggesting that at least some exposure to open air occurred, but such exposure may have been intermittent and relatively brief.  Still what explanation can be given for the microscopic pitting and frosting of the grains of sand? It turns out that desert sand is not the only sand that can be pitted and frosted. The chemical process of sand cementation in the forming of sandstone can also cause pitting and frosting.70

So, it appears that the evidence does not fit the classic dry desert formation of the Coconino Sandstone layer over millions of years of time.  Many of the trackways may even have been formed underwater or at best on long standing damped sand dunes where all the creatures walked only uphill.  Ocean currents can and do make very pure quartz sand dunes with specific characteristics that match the dunes in the Coconino Sandstone.71 Heavy ocean currents can in fact amass huge quantities of sand in a very rapid timeframe. The sand dune angle found in the Coconino Sandstone layers would require a depth of water of around 300 feet and a fairly brisk current.  In such a scenario, large dunes with cross bedding can be made very quickly.

Consider also that there is no significant erosion between the Coconino Sandstone layer and either the layer above it (the Toroweap Formation) or the layer below it (the Hermit Formation). All of these layers formed like sheets of glass - one on top of the other.77 Isn’t it strange that significant portions of these layers have not been weathered away to be filled in by overlying layers in an uneven way? In fact, large contraction cracks penetrating deep into the Hermit Formation (just below the Coconino layer) are filled in with Coconino sandstone.  If the Hermit Formation took millions of years to form, which would surely turn the layers in this formation into solid rock in a small fraction of this time, how did such deep cracks form in solid rock in such a way that the surface was completely flat and yet the cracks themselves were filled with pure Coconino sandstone?  One would think that if such formations and characteristics took long periods of time to form that the boundary between the Hermit Formation and the Coconino sandstone would have been blurred by "bioturbation", disturbed in an uneven way by erosion, and that the cracks found in the Hermit shale would have been filled with other contaminants besides pure Coconino sandstone.  But, these findings are not strange if the layers were all formed relatively rapidly by water deposition instead of over vast expanses of time. Which theory has better explanatory value? (Back to Top)




Subjective Taxonomic Classification




       Since a single gene pool can produce "drastic" differences in phenotypic forms, how are scientists so sure of their fossil classification models?   Often only slight phenotypic differences are enough to place a fossil creature in a different species, genus or even family group than its modern-day counterpart or than its counterpart found elsewhere in the geologic column.  The problem is that differences, even fairly significant differences, are known to exist between members of the same gene pool.  Because of this fact, taxonomic classification models can be quite subjective and even misleading.

       For example, scientists from Berkeley have noted that, "the planktonic larvae of many marine invertebrates are commonly described as separate species when they are first discovered in the ocean. Only later when they can be reared in the laboratory can the link to their adult form be recognized. Similarly, the different life stages of many fungi are given different names because they have different physical forms and hosts. Only through detailed inoculation studies can mycologists work out which forms are members of the same life cycle. Since some fungi may have more than five discrete life cycle stages, this can be a long process. Similar problems exist for some marine algae and multiple-host parasitic organisms of many kinds. Even among well-studied vertebrates, some tropical birds have been described as separate species until they are observed to mate and rear young together."24

       "Detailed study of large sympatric populations and fossil assemblages of the highly variable species Elphidium excavatum (Terquem) [Benthic foraminifera] collected from 20 widely spaced locations indicates that a variety of morphotypes of Elphidium can be linked to one another in a number of interlocking intergradational series. Ten morphotypes are recognized and grouped as formae (ecophenotypes) of Elphidium excavatum (Terquem); these morphotypes were previously considered as 22 independent taxa by various authors… Although all of these formae belong to the same species, it is suggested [by the authors] that the distinction among them should be retained because of their potential as a valuable interpretive tool in paleo-ecological and biostratigraphic studies of Holocene and Pleistocene sediments."25

       "Because they are based on different stages in the life-cycle, fossil dinoflagellates and living dinoflagellates have largely received two sets of names, the equivalencies of which are becoming increasingly well known. For example, Gonyaulax spinifera (the “type species” of Gonyaulax) and related species are known to produce cysts assignable to the genus Spiniferites. Indeed, it is generally informally acknowledged that Spiniferites and Gonyaulax are taxonomic synonyms. For several reasons this synonymy has not been formally proposed: 1) the fossil generic name Spiniferites is senior to the extant name Gonyaulax and acceptance of the synonymy would bring considerable changes to the nomenclature of this major extant genus (and conservation of Gonyaulax would cause a reciprocal chaos among fossil names); 2) the exact correspondence of Spiniferites species with Gonyaulax species is not clear; and 3) it is impossible to establish whether earlier representatives of the genus Spiniferites were cysts with a thecate stage identical to living Gonyaulax. In other words, to many researchers, it is useful and desirable to retain both Gonyaulax and Spiniferites while acknowledging that they may represent the same biological taxon."26

       The naming of hominid fossils not immune from this subjective problem.   In a March 2002 statement, Tim White, who co-directs the Laboratory for Human Evolutionary studies said, "There’s been a recent tendency to give a different name to each of the fossils that comes out of the ground, and that has led to what we think is a very misleading portrayal of the biology of human evolution… But when you find a fossil like this one so similar to Asian and European ones, it indicates the same species." "This whole species question is all about what you accept as a sharp enough distinction to tell you that it is a separate species," said Susan Anton, a Rutgers University anthropologist. "This particular skull is not going to solve that problem."27

       Specific hominid fossils, such as the Solo fossils, have presented a bit of a problem as far as classification in concerned. "When they were first discovered, von Koenigswald believed them to be "tropical Neanderthalers." In 1963, Bernard Campbell classified them as Homo sapiens soloensis. Santa Luca, in 1980, classified them as Homo erectus erectus, with Milford Wolpoff declaring that they were not Homo erectus. Still others called them "archaic Homo sapiens." Because of their obvious similarity to the other Japanese and Chinese "classic" Homo erectus material, most investigators today recognize them as Homo erectus. The Solo fossils do, however, have a larger cranial capacity than does the average Homo erectus skull. For this reason, many evolutionists could not resist the temptation to consider the Solo people as "transitional" between Homo erectus and modern humans. Unfortunately, since evolutionists believe that modern humans arrived on the scene by 100,000 YBP, transitional fossils at 27,000 YBP will not fit…  It is now known that there are many late-date Australian fossils almost identical to the Solo (Ngandong) people."28

       The classifications of plants is classically prone to give different names to very similar plants or even parts of the same plant.  Bill DiMichele, a paleobotanist, notes, "The problem of organ association is one of the reasons why paleobotanists insist on so many different names for isolated parts of the same whole plant. Furthermore, there are phenotypic convergences that can cause great confusion, such leaves of virtually identical morphology borne on ferns and seed plants. Separate names for each fossil plant organ can be carried to extremes, however, and not all paleobotanists, myself included, favor the attribution of separate names to organs otherwise known in attachment (yes, this is still done routinely, no kidding)."29

       The Mazon Creek flora is incredibly diverse. Over 400 species from at least 130 genera have been identified from Mazon Creek nodules. However, the number of different kinds of plants represented is very difficult to determine. There are at least two reasons for this difficulty. The first reason is the convention among paleobotanists that separate plant parts receive different names. This procedure tends to inflate the number of plant names. The second reason is that paleobotanists are still trying to determine which taxa are valid.30 

       According to Meyen and Traverse the problems of naming fossils are as follows. "1. Living plants are assignable to a single taxon at any rank whereas fossil plants with dispersed parts and no observable original connections may be referred to several taxa of the same rank and have different names (Stigmaria, Lepidodendron, Lepidostrobus) 2. In living plants, all individuals belonging to a species belong to the same genus, etc. whereas in fossil plants various specimens of a species may or may not belong to the same genus and the genus may belong to different families when the complete plant is considered (Stigmaria may belong to genera assigned to Lepidodendraceae, Sigillariaceae, or Lepidocarpaceae). 3. Living plants are assigned to a complete hierarchy of taxa whereas fossil plants may be assigned only to genera with higher rankings unknown (some leaf genera might belong to pteridosperms, ferns, or cycads). 4. Living plants cannot be assigned to different genera based upon different types of preservation whereas fossil plants may be. 5. Different ontogenetic phases of the living plant do not normally serve as a distinction for a taxon whereas in fossil plants this is possible (seeds, microspores, megaspores, cysts). They concluded that fossil plant nomenclature requires only two special circumstances be reflected in the ICBN: 1) the possibility to keep genera of fossil plants outside the hierarchy of formally named higher taxa; and 2) the possibility to retain names of taxa established for various parts."31,32

       As it turns out, "Intraspecific variation is ubiquitous in systematic characters, yet systematists often do not deal with polymorphism explicity. For example, morphological systematists typically exclude characters in which any or "too much" polymorphism is observed, and molecular systematists often avoid intraspecific variation by sampling a single individual per species. Recent empirical studies have suggested that polymorphic characters contain significant phylogenetic information but are more homoplastic than fixed characters… Excluding polymorphic characters decreased accuracy under almost all conditions examined, even when only the more variable characters were excluded. Sampling a single individual per species also consistently decreased accuracy. Thus, two common approaches for dealing with intraspecific variation in morphological and molecular systematics can give relatively poor estimates of phylogeny."33 (Back to Top)












       Foraminiferans are actually protozoans (single celled animals) of the Order Foraminiferida.  Their fossilized remains have been commonly used to relatively date sedimentary rock.  This practice is especially extensive in the oil industry.  These creatures are usually quite tiny, but have a fairly wide range of size from 0.1 millimeter (mm) to almost 20 centimeters (cm) in length with an average that is less than 1 mm. They also have an extraordinarily fast doubling time of 3.65 days.  The parts of the creatures that are preserved in the fossil record are their shells.  Actually, these shells are not really shells in that they are "intra-ectoplasmic" structures called "tests".  These tests function somewhat like a skeleton and are formed of small interconnected chambers.  The chamber connections are small openings between each chamber.  The openings are called "foramina" from which the name "foraminifers" comes from.  Foraminiferan shells or tests come in many shapes and sizes and have many different designs to include simple tubes, straight series chambers, coils of chamber and even complex labyrinths.  Their walls can be formed by particulate matter picked up from the surrounding environment or they can be formed of pure calcareous material that is secreted by the foraminifer.  Foraminifers interact with their environment through pores and apertures that exist in the test wall.  Their taxonomy is based first on the wall mineralogy and microstructure, then on chamber arrangement, apertural shape and position, and finally ornamentation. 21,22

       Foraminifers are not only abundant in the fossil record but live today as well.  They can be found practically anywhere where there is a body  of water to include deep sea trenches, shallow seas and oceans, and even fresh water lakes.  However, different types of foraminifers occupy different types of environments.  For example, planktonic and pelagic species live in open water at various depths while benthic species live near, on, or in the ocean floor.  In deep ocean environments, calcareous (made of calcium) material is dissolved, so foraminifers in this environment tend to be of the type that agglutinates surrounding material to make their tests instead of forming calcareous tests.  Foraminifers move around via "pseudopodia" or hair-like extensions of protoplasm and have been clocked at several millimeters per hour.  These are also used as "arms" for the gathering of food and building materials and for attachment to other objects.  Sometimes the pseudopodia are even used to aid in floatation, as is the case with planktonic species.  Foraminifers can also tolerate extreme environments to include very low oxygen levels, hyper- and hypo-salinity, as well as extremes of pH and temperature.  What is interesting is that these different environments play a role on the type of framiniferan that occupies a particular area.  For example, areas with low oxygen levels have foraminifers with a more flattened shape to increase absorption surface area.   Their walls also tend to be thinner, more porous, and less ornamented. 22





         So, what do these very interesting creatures have to do with the theory of evolution?   Well, as previous hinted at, different foraminifers are found in different layers within the geologic column.   In fact, some are so closely associated with a given layer that when they are found, they practically define that layer within the geologic column.  This association is so reliable that oil drilling companies rely heavily on the identification of these creatures as they drill their wells to the proper depth.  Obviously then, if the layers in the geologic column represent long periods of historical time, the differences in foraminifers represent evolutionary changes over time.  The layers could not possible have been formed rapidly by a watery catastrophe such as are mentioned in flood legends, for how would these foraminifers, who are similar in size and density, be sorted so neatly into the various layers in which they are found?  There are some, such as the geologist Glenn Morton, who argue that:  


      "Foraminifera are small, single cellular animals which would have existed in the oceans prior to the flood and due to their small size should be found all mixed together in the same or closely related strata...   Given the small size of the average species, they should all sort out at about the same time from the waters of the flood with the largest at the bottom and the smallest at the top.  This is not what we find when we look at the foraminifera fossil record. Genera of forams, all possessing the similar shape and similar size and only differing in the details of the test decoration, are found over vast vertical distances in the geologic column...  It is like throwing similar size and density sand particles, which are colored different colors, into a river and having the colors all sort out. This is impossible. Yet forams are so sorted. The only conclusion can be that their order is not due to a global flood but to a long period of deposition in which the animal life changed." 21    


       Morton's argument is especially interesting when one considers that different foraminiferan test decoration are found within the same species depending upon environmental factors of the local habitat.  Tammy Tosk, also a geologist, argues that both habitat preference as well as environmental factors can have a rapid impact on foraminiferan morphology.22  Consider the following illustration and note that the foraminifers of today vary in morphology according to changes in ocean depth.  






       As illustrated above, Tosk argues that morphologic variation or "sorting" within the geologic column can be based on normal ecologic distribution.  Tosk goes on to argue that within a single foraminifer species, certain members may have thickly ornamented tests under normal oxygen concentrations and thin less-ornamented tests in environments where oxygen concentrations are low.  Such variations that are based, not in genetics, but in environmental influences, are called "ecophenotypic" variations.  Based on these ideas, Tosk theorizes about how the geologic foraminiferan data could be explained by a rapid catastrophic burial:


      "Because of the many examples of variation in living and fossil forms, foraminifers are considered to be extraordinarily plastic (Kennett 1976). A foraminifer may contain enough genetic information to express many different forms, depending on the conditions...  A significant problem arises because similar forms are classified differently if they occur at different stratigraphic levels. These cases are explained as iterative evolution, that is, the same form evolved repeatedly through geologic history. Thus classification is subjectively influenced by evolutionary theory. Repeated occurrences could be explained as easily by a catastrophic flood model. If the foraminifers found fossilized at various levels in the geologic column were living at the same time in different ecologic zones, species common to several ecologic zones would be found at several levels. Gaps in the record only indicate that the species was not present in the source area or the ecologic zone being buried at that time, not that it was totally extinct. No coincidence of repeated extinction and identical evolution is required.  

       Ecologic zonation as developed by Clark (1946) would mean that foraminifers living in the lower seas or deeper parts of the ocean would be buried first as the sediments were redeposited by the gradually rising flood waters, while those from higher ecologic zones would be buried later The fossil record seems generally consistent with this model. [The figures above] show the distribution of foraminifers today and of fossils in the geologic column. Simple agglutinated forms that now live in environments ranging from the deep sea to estuaries, are found fossilized in Early Paleozoic and younger strata. Calcareous benthic species now predominate both in bathyal environments and in Mesozoic strata of the past, and presently floating planktonic forms from a higher ecologic zone are abundant in the higher Cenozoic strata of the past.

       In the oceans today, calcareous material is dissolved below the carbonate compensation depth (CCD) — usually at a depth of about 4000 m, depending on carbon dioxide concentration. Neither benthic nor planktonic calcareous foraminifers are generally found below that depth on the abyssal plains or in deep sea trenches, because their calcareous shells would be dissolved. Agglutinated forms are dominant

       Agglutinated species are common in the Lower Paleozoic, and the benthic calcareous foraminifers found generally have thicker walls than forms higher in the geologic column. They could have lived near the pre-flood CCD where most calcareous forms, especially thinner-shelled planktonic species, would have been completely dissolved. Lower Paleozoic foraminifers are consistent, therefore, with the distribution expected by a catastrophic flood.

       The fusulinids in the Upper Paleozoic, however, are an anomaly. Some species of fusulinids grew to volumes of more than 100 m3 (Ross 1979). Foraminifers which grew that large today have symbiotic photosynthetic algae living in their tests, and so must live within tens of meters of the ocean surface where sunlight is available. Large foraminifers from other groups live in shallow water tropical environments today; therefore, the fusulinids are interpreted also to have lived in a similar environment (Ross 1979), yet we do not find them at the top of the geologic column. Possibly they grew at the surface of pre-flood bodies of water of low altitude (Figure 1).
       Planktonic foraminifers are not found in Paleozoic or Lower Mesozoic deposits. Even though living planktonic foraminifers float and would not be expected to be found in the early flood deposits, tests of those which had died before the flood should have been on the sea floor and should have been buried with those living there. Either they were not present in those ecologic zones, or they were not preserved as fossils. Because they have thinner, more porous tests than benthic forms, they could easily have been dissolved preferentially on the sea floor before the onset of catastrophic flooding, if their shells sank below the CCD.

       Benthic hyaline calcareous foraminifers become abundant in the Mesozoic. Triassic and Jurassic foraminifers are generally not as well preserved as later forms. In Cretaceous strata, both benthic and planktonic forms are diverse and abundant, making it correlative with the upper bathyal zone of the ocean today.
       Foraminifers older than the Cretaceous are generally widely distributed. A Triassic species may be found in both Australia and Idaho, but nowhere in between (Tosk and Andersson 1988). Cretaceous and younger foraminifers have distribution patterns correlative with modern assemblages (Sliter 1972). Under the prevailing paradigm, this would mean that the pre-Cretaceous seas were more cosmopolitan because modern hydrographic patterns and ecologic distributions had not yet developed. Continental fragmentation and sea-floor spreading during the Cretaceous are used to account for the development of modern oceanic patterns at that time.
       In a flood model, however, this pattern is what would be expected. During the more violent stages of the flood events, foraminifers from a small area would be scattered widely over the earth. As the violence of the flood died down, foraminifers would not be transported as far and might even begin developing their own ecologic distribution patterns. Major deposition during and after the Cretaceous could have become localized in basins and at continental margins. Life for foraminifers may have returned to normal in less affected areas." 22


       So, it seems at least possible to conclude that the apparent "sorting" of foraminifers in the fossil record could have occurred outside of slow process of millions of years involving gradual evolutionary changes.  Morphologic variations seen today are often based on ecologic environment that are fairly distinctly "sorted."  Arguments such as Morton presents need not necessarily or even preferentially support the long age scenario over a catastrophic formation of much of the geologic column. 

       But what about arguments that Morton also raises that foraminiferans show smooth evolution between species?  Consider the series of slowly changing forms presented at the right.  Morton refers to this series as a clear example of plankton evolution in action by saying,



      "One can clearly see the gradual transformation of the earliest into the latest species.  This gradual change is imperceptible...  Gradualistic evolution is documented among these tiny creatures laying bare the false claim that there are no transitional forms. What it shows is that the flood-advocates don't read anything except their own literature."  21


     Well, after reading Morton's "literature" it seems that such variations in morphology might be easily explained by variations in environment.  These forms pictures at the right might in fact be members of the same species of plankton.  After all, foraminifer are quite "plastic" indeed.  The genetic information contained in one common gene pool seems quite capable of producing startling morphologic variations.  Considering this ecophenotypic variation potential, how then is Morton so sure that "gradualistic evolution" is taking place here? (Back to Top)















Pollen Order




       Some point to the obvious vertical order of pollen found throughout the fossil record and suggest that such sorting can only be explained by evolutionary changes over time.21  It is true that pollens are also sorted in the fossil record.  However, to say that this sorting is impossible for a large complex fluvial event or a relatively rapid series of rather complex catastrophic events to explain, seems to be a bit presumptuous. 

       As it turns out, different pollens can be water sorted based on various characteristic differences such as size, specific gravity, density, chemical composition (ie: hydrophobic vs. hydrophilic), and "fall velocity" in water.  For example, most deciduous pollen types sink in water in a few minutes while bisaccate grains (pine pollen) float for much longer times, sometimes years, before they sink."  Pohl (1933) noted that pine pollen could retain its buoyancy for up to four years… 

       Hopkins’ (1950) results show that there is some differential buoyancy between Pinus species.    The grains that sank are those with smaller or deformed/broken air sacs.  When placed on a water surface in a large water tank, over which a breeze of 13km/h was blown, conifer pollen drifts at a rate of 0.16 to 0.32 km/h.  When oak pollen (Quercus palustris) was put through a similar process most of it sank within the first meter… 

       Bisccate grains will only sink if the bladders are pierced either by physical, chemical or microbial processes.  They are therefore more likely to be saturated if they enter turbulent flow, or if they have been resident in a position (such as the soil surface) where they are open to microbial attack prior to introduction to the water…

       Many pollen grains have mechanisms to prevent desiccation, but cannot prevent water uptake.  Sporomorphs, many of which have no openings in the exine, have no inlet for water.  Some, such as Lycopodium, also have an oily coat (Balick & Beitel, 1988).  Attempts to saturate Lycopodium in the laboratory have shown that such grains are extremely resistant to water uptake.  Extreme methods have been invoked, such as placing the sporomorphs in a beaker in a vacuum for up to eight hours (own method) or boiling in water (Reynolds 1979).  This means that they are likely to remain afloat in the water, in nature, for long periods of time.  This is consistent with results from the Volga River where Fedorova (1952) found Lycopodium spores over 7000km from their source…

       Several authors have found that water currents can sort sporomorphs.  This was first seen in the field by Muller (1959) who was looking at the palynomorph distribution in recent sediments in the Orinoco delta area.  He noted that the pollen of Rhizophora, which is relatively small, was carried further out to sea than larger sporomorphs from similar source areas. 

       Cross et al.  (1966) also found evidence of sorting in a marine setting as lighter, more buoyant, grains were carried further toward the southern end of the Gulf of California… Davis et al. (1971) and Davis and Brubaker (1973) explained differences in the distributions of oak (Quercus) and ragweed (Ambrosia) in the sediments of several small North American lakes as resulting from sorting.  The smaller ragweed grains remain in suspension for longer periods of time, allowing them to be transported to the littoral areas of the lake by wind generated currents.  Sorting was also used to explain results presented by Chen (1987) from the sediments of lake Barine in Queensland, Australia…  Larger grains are deposited in the littoral areas, while smaller grains are carried to the lake center by these currents.  

       Clearly sorting of sporomorphs can occur in many depositional environments.  The behavior of sporomorphs as sedimentary particles is, however, poorly understood… In a more recent study of alluvial sediments from a canyon stream in the chuska mountains of Arizona, Fall (1987) tested the assumption that the pollen in the alluvium was from local vegetation.  She found that pollen concentrations in general were highest in the fine-grained sediments.  Non-arboreal sporomorph types however were found in higher numbers in the sandy sediments.  Similar results have been reported from Glacio-lacustrine sediments in Alaska (Goodwin, 1988) and braided stream deposits adjacent to the Caribou River in Yukon (Catto, 1985) or they may be due to different source areas of tributaries involved.  These results suggest that the deposition of fine-grained sediments, sporomophs in particular, is related both to the flow conditions of the water and the bed material over which the water flows.

       From the evidence presented here is it suggested that, where water currents drop below 35cm/sec, sporomorphs may be sorted. This sorting is primarily due to size, but sporomorph density is also important." 23 (Back to Top)






Stacked Forests










Many will argue that in different places throughout the word, there can be found layers of “forests” one on top of each other, with their trees, “in the position of growth” (still standing up).  It is also said that these forests each have their own layer of “soil”.  So, it is felt that each of these were forests grew over long periods of time on top of previous forests, each of which was buried by some long ago catastrophe.  What is interesting about these places (ie: Yellowstone National Park were up to 65 different layers can be found with trees in the vertical position)13 is that the trees are still oriented in their positions with each other.  Their “soil” is also found to be water sorted (course to fine), and often is found half way up a tree instead of at its base.  This organic material also averages only 3 cm in thickness and, for many of the "forest" layers it is missing altogether.  In some areas, such as Mt. Hornaday, as many as 43% of the forest layers have no organic layer at all.  The lower layers of Specimen Creek generally do have organic layers (96%), but the upper layers of Specimen Creek have far fewer organic layers.  It turns out that the average "forest" without an organic layer to is about 24%.  It seems rather strange for a forest to grow into full bloom without forming an organic layer.  How is this explained?  

Another strange finding of the organic layers is the fact that they are sorted in various ways.  Take for instance the fact that pine needles and leaves are not mixed together, but are found in separate organic layers despite the fact that there are both pine and hardwood trees "growing" from the same organic layer(s).  Also, the are proportionately less pine needles than there are leaves even in areas that are dominated by conifers.  In a real forest, conifers drop a much higher mass of needles than deciduous trees drop leaves.  And yet, in the fossil forests of Yellowstone, needles are relatively sparse even at the bases of large fossilized conifers.  This interesting fact has been recognized as far back as 1899 when Knowlton remarked about the absence of needles in the organic levels associated with the large fenced petrified tree near Roosevelt Lodge in Yellowstone National Park. 15 One would expect to find great numbers of sequoia needles and some cones, since most of the upright trees are sequoia (70%). However, large numbers of broad leaves and only a few pine needles are seen in the organic levels. Sequoia needles were rare or absent. Although petrified sycamore stumps are not common, leaves of sycamore are the most abundant broad-leaf fossils.  It is also interesting to note that, despite a heavy predominance of sequoia trees, fossilized sequoia cones are very rare in the fossil forests of Yellowstone National Park.  This taxonomic sorting seems quite strange indeed unless one uses a catastrophic model involving flood such as occurred during the eruption of Mt. St. Helens.  In water, pine needles become saturated and sink before leaves sink.

  Pollen is another problem.  Trees with wind-transported pollen, such as walnut and sycamore, should have left a pollen record in the forest floor, but little or no pollen of these two has been found.  Modern forest floors contain pollen in abundance inversely proportional to the distance from the source trees especially trees for which wind is the pollen-transporting agent. Research done on four levels of Specimen Creek Petrified Forest showed no positive correlation between fossil pollen abundance and the proximity of possible source trees.18

The organic layers themselves also show no significant decay as one goes from top to bottom.  In a real forest floor, organic material decays.  Evidently, this does not happen in the forests of the past because the leaves at the bottom of organic layers are just as well formed as preserved as the leaves at the tops of these organic layers.  Also, the material between the leaves is sorted, course to fine as one moves upward (Consider the figure at the right).  Evidence for such water sorting occurs in about 70% of the organic layers.  

There is yet another problem with the intermittent burial of forests by volcanic activity and mud-slides.  If a volcanic mud slide buried only the lower parts of the trunks of the trees of a growing forest (as might be suggested by the fact that some of the upright trees penetrate overlying layers), the taxonomic composition of the new forest that grew on this new surface would be similar to the composition of the forest that was buried. The cones, seeds, nuts, and fruits would fall from the unburied branches and foliage and repopulate the new surface with a similar forest. Such correlation between adjacent levels of the Specimen Creek Petrified Forest has not been found.18 

The normal maturation of soil also involves the slow breakdown of feldspar and other minerals into clay.  Out of 65 layers of Specimen Creek in Yellowstone National Park, only nine bands of clay were found among only seven organic layers.  Horizontal sampling of two of the clay bands at 2.5 - 3 m intervals for 30 m showed a constant mineral distribution. Abundant unweathered feldspar is scattered throughout the Yellowstone organic levels, suggesting repeated rapid burials.19 None of the 58 organic levels outside the 9 bands of clay contained detectable amounts of clay. The apparent absence of clay in the majority of levels (implying that normal weathering of soil did not occur) raises questions about the passage of long time intervals between levels. This datum also questions the validity of the assumption that the organic levels (upon which trees with hundreds of rings sit) represent true soils. Furthermore, the sudden abundant appearance of clay in a few horizontal bands that included both organic levels and layers of clay in the associated breccia beds between levels suggests transport rather than in situ formation of the clay minerals.

Despite much study of the Yellowstone Petrified Forests, no animal fossils have been found. Why are animal remains absent from the plant fossil-bearing levels of Yellowstone? Because forests would be expected to harbor a wide variety of animals, some of which would be buried by the successive mud slides, the absence of animal fossils has been a mystery. Volcanic activity could have caused larger forest animals to flee elsewhere, but flight cannot be used as an explanation for the absence of all animal remains because many animals could not or would not leave their forest habitats. Land snails, some amphibians and reptiles, many insects, arachnids, and worms would not escape burial. Immature members of many types would be unable to flee. In addition, bones, eggs, teeth, scales, molted skins, castings, droppings, burrows, etc., would qualify as evidence of animal life. None of these have been found in the fossil forest organic levels during a century of research. Considering that delicate plant parts are excellently preserved, animal remains should also have been preserved if they were present. Only one exception is known. Remains of termites have been found in chambers within the petrified wood.19  If the petrified trees are standing where they originally grew and if the organic levels are the growing surfaces still intact and undisturbed, the absence of animal fossils is difficult to explain. If, however, the trees and the organic debris making up the soil levels were transported by water, the separation of animals from the plants before burial is much easier to explain. 

The volcanic ash found in the various layers is itself is quite interesting.  The chemicals that make up the ash are uniform throughout all the layers.  In fact, there are only four unique chemical patterns to be found in the ash of Specimen Creek.  Spark source mass spectrometry analysis of trace elements in the bands of ash revealed pulses of ash from four source areas for the Specimen Creek Petrified Forest.  The four trace element profiles interweave in an irregular manner up the sequence of 65 organic levels of Specimen Creek Petrified Forest. If these 65 ash layers (organic levels) were laid down over a long time span, the ash that was laid down thousands of years later near the end of the series of ash eruptions would have changed sufficiently to produce a new and different trace element profile (a new "fingerprint"). This has not been the case. The rapid burial of the whole sequence seems to be required. 

The root systems of the upright stumps seems to be a main argument in favor of their in situ growth.  Of course, some of the petrified trees have broken roots; but when were they broken? Even if a permit to collect petrified wood within the park is obtained, excavation of stumps is not permitted; furthermore, digging is difficult in the hard rock. Consequently, to determine if the root breakage seen is pre- or post-petrification is difficult. Several examples of abrupt root terminations from Mt. Hornaday, Mt. Norris, Tom Minor Basin, and Specimen Creek strongly indicate that, at least in some cases, the tree roots were broken before the trees were buried by volcanic gravels and muds. This evidence supports the view that the trees were transported.  However, small rootlets can be located at the bases of upright stumps, and this feature has been used to argue against transport.  Observations in Spirit Lake near Mount St. Helens and of trees uprooted by bulldozing operations show that the small roots and rootlets are usually still intact, but the larger roots are usually broken (See Figure).  The presence of small roots extending from the base of a petrified tree therefore is not evidence for an in situ interpretation unless large roots also extend unbroken. Broken and frayed large roots could be the result of changing stream currents eroding the bases of growing trees, but such activity should leave evidences in the sediments. Furthermore, erosion must be limited; otherwise, trees would be removed or toppled.

If a forest were killed by a mud flow that buried the bases of the trees, the tops of the trees would extend above the new ground surface. They would overlap a new second forest that would commence growing on the new surface. During the time of the growth of the new second forest (before it in turn was buried by another volcanic mud slide) the old first forest snags would have time to rot, to be infested with insects, and to break drown. Even the tops of stumps that reached only to the root area of the second forest level (no actual overlap) would also be expected to experience decay. The soil in which the roots of the second forest grew would not be a good preserving medium for the tops of the stumps extending up from below. One of the striking features of the Yellowstone petrified trees is their good preservation. If pieces of the petrified wood are prepared as microslides, the wood tissue may look nearly as fresh as tissue from a living tree. Seldom do they exhibit any evidence of decay and weathering.19 This suggests that the trees have not been subjected to these processes during the passage of time.

The parallel orientation of the horizontal logs, mentioned earlier, is better explained by water or mud transport. The dip of the beds from which the trees arise seldom exceeds 7° which is not enough to cause all the trees to fall downhill.19 Prevailing winds or volcanic blasts could align fallen trees, but they would not cause the long axes of the cross-section of the upright stumps to have a similar compass alignment. The asymmetry of the cross-section of a stump, especially at its base, is usually a result of the influence of major roots that cause flare to extend for some distance up the stump. Volcanic lahars (fast-moving volcanic mud slides) or currents of water or mud could be the forces that acted on roots and trunks to produce similar alignment for both stumps and logs. Modern forests do not show the degree of orientation that the fossil forests of Yellowstone show.  This orientation seems to speak for catastrophic transport and against in situ forest growth.

One of the first observations made when research commenced on the petrified forests was the barkless condition of both the horizontal and upright trees. Subsequent examination has revealed some thin layers of bark remaining on a few of the trees. In addition to the trees being mostly barkless, all the branches have been broken off. Even large branches, 25 cm or more in diameter, have been removed. Only scoured stubs remain on the tree trunks. Trees buried and later excavated by water erosion during the eruption of Mount St. Helens did not have all the bark or limbs removed. Trees floating for a period of time in turbulent water would more likely lose bark and branches due to softening of the bark and abrasion.14,15 Considering the fact that modern trees often sink in water in the vertical position, a catastrophic model seems to be the best explanation for these findings.16  A massive flood, burying layer upon layer of sedimentary material in quick succession, seems to be at the very least, plausible.  

The eruption of Mount St. Helens and the resultant flooding in locals such as Spirit Lake might offer some insights into how the stacked forests of Yellowstone might have formed.  The floating log raft in Spirit Lake does in fact provided some insights on taxonomic sorting. Most of the stumps sitting erect on the bottom of Spirit Lake are Silver Fir, Nolle Fir, and Hemlock. Douglas Fir, abundant in the surrounding forests, has only 2.2% representation. Sampling of the trees in the floating raft solved this discrepancy; 48% are Douglas Fir. Apparently this species is more buoyant and resistant to water saturation. Cedar was represented by 2.2% of logs floating in the lake; yet the surrounding forests contained a higher percentage of cedars. Sampling of the broken wood pieces along a transect on the shore gave 11% for cedar. Some of the erect trees floating in the lake or standing on the lake bottom are over 20 m tall. The argument that tall petrified stumps must be in position of growth does not apply to a flotation scenario. The flotation of organic matter (including trees in an upright position) as illustrated in Spirit Lake at the base of Mount St. Helens provides a model for interpreting the upright petrified trees of Yellowstone. Trees and plants will float vertically when there is sufficient water and time. The research at Spirit Lake helps explain the presence of the organic layer at the level of the roots. Saturated organic debris sinks to the lake bottom to produce a layer of organic matter. Upright floating trees also have dropped out of suspension onto the bottom of Spirit Lake in a spacing pattern similar to that of growing forests. They are not jumbled together in log jams as might be expected. 20 

Some have argued that Spirit Lake is not a good analog for the Yellowstone Fossil forests, because the large number of logs accumulating on the bottom of Spirit Lake very different from the more scattered fossil logs and stumps in Yellowstone. However, one important difference between the two deposits is that Spirit Lake has not had adequate sediment input to bury the sinking logs and stumps. If the 1980 Mount St. Helens eruption had been followed by a series of volcanic breccia flows into Spirit Lake, spaced long enough apart to bury successive sets of logs and stumps as they sank, it would likely have produced a deposit very similar to the Yellowstone Fossil Forests.19

If this is not yet convincing, these same trees were studied to see if they might have matching patters of growth in a tree-ring analysis.  Matching patterns of growth would be highly unlikely if the trees lived thousands of years apart in time.  In 1991, Dr. Michael Arct presented such a study for his PhD dissertation (building upon research that he had been doing since 1979).  He sampled fourteen fossil trees at different levels in a twenty-three foot section of the Yellowstone formations.  Analysis showed that all fourteen trees matched and that ten of them died at the same time.  The other four trees died seven, four, three, and two years before the other ten died.  The theories of ancient formation no longer seem to match the facts available.7, 8 (Back to Top)







Fossil Orientation




It is quite interesting to note that fossilized trees are not like  one would expect from the normal evolutionary picture of what happened.  According to current popular scientific belief many fossilized trees were buried naturally either as they lay fallen on the ground or as they stood growing.  However, what is unique about almost all fossilized trees is that they do not have roots or branches and little if any bark.1, 3  Also, the ones that have fallen and that are laying horizontally, align themselves in the same direction.1, 3   Also, many fossilized seashells and tree leaves are oriented relative to each other throughout the  fossil record.  The trees in the forests of today do not do orient themselves when they fall.  When they fall, they fall in a fairly random way without a statistical significance  in their orientation. This is not so with petrified trees. Petrified trees all line up.  Even the vertical ones have a particular orientation.1 What could have caused these trees to loose all their roots, branches, and bark and to line up in the same direction as every other tree in that layer?  During the floods of Mt. St. Helen’s eruptions, the trees did exactly the same thing.  

They lost all their roots, branches and bark, and were all lined up in the same general direction, even the ones that sank into the lakes vertically.  Fossilized trees can be found throughout the entire world and they all do the same thing.  Scientists at the National Petrified Forest in Arizona freely speculate that the petrified trees of that “forest” were “washed”  into their current positions judging from the fact that they generally have no branches, roots, or bark.3   They all appear as though they were in some sort of catastrophe together.  This is clearly visible to all who visit such petrified forests.1 

Such "current" orientation is found throughout the fossil record, with orientation of fossils being observed over vast areas, sometimes hundreds of thousands of square miles.  Although not all fossils show current orientation, a sizable percentage do show such current orientation.  Clearly, such orientation on such massive scales as are found throughout the fossil record are not consistent with slow sedimentation and burial, but rapid burial by the heavily silted currents of a large and sometimes massive fluvial event or series of closely spaced events. (Back to Top)






Polystrate Trees






Yet another interesting finding concerning petrified trees, is that many of them extend vertically through millions and millions of years of sedimentary rock.  How can this phenomenon be explained?  A common explanation is that these do not represent areas of the standard geologic column, but areas of rapid local flooding and sedimentation.  Therefore, the layers that these trees pass through do not represent thousands and millions of years.  However, the pictures shown to the right are of a petrified tree (located near Katherine Hill Bay  next to Flat Rocks Point, Australia) extending up through many sedimentary layers and  through two separated coal seams.4  The tree itself is twelve feet tall, and was uncovered by a coal mining company.   If the two separated coal seams represent long periods of time, how could this tree be extending between them both?  It seems to me that this is a difficulty for the current understanding of science.  Notice also that the layers themselves show no weathering between one layer and the next even though each layer was supposedly the surface of the earth for thousands if not millions of years.  These combined mysteries are more easily explained by rapid underwater burial with quickly forming sediments.  The theory that each fossil bearing layer in the geologic column represents eons of time seems inadequate to explain such problems that are easily explained by a quick catastrophic event. (Back to Top)








Coal Formation






Coal itself is a problem.  According to modern science, coal forms from peat bogs.  Over a great many years, the peat becomes thicker and thicker.  After being covered by a sedimentary layer, the immense pressure and heat combined with water, changes the organic material chemically into coal.  It is thought to take about 6 feet of organic material to make one foot of coal.  However, this theory has trouble explaining a few interesting facts.  Coal seams, such as those found in the Powder River Basin of Gillette, Wyoming, ranging from 150 to 200 feet in depth, point to a rapid coalification process. "These coal seams run remarkably thick and unsullied by other material. Usually, unwanted sediments, such as clay, washes over a deposit before coal seams can get very thick. This leaves scientists with the baffling question of how the seams get so massive and still remain undiluted by influxes of clay and other impurities (such as sulfur etc.) before they thicken."5  This is quite a mystery considering the fact that a seam of coal 200 feet thick would have taken a layer of organic material over 1,200 feet thick to create it.  That is a lot of peat to be in just one area.  But, what makes this even more unbelievable is that the Powder River Basin covers an area of over 10,000 square miles.  This problem could be solved with the idea of a massive flood deposition of huge quantities of organic material in a very rapid timeframe.  Similar deposits of huge amounts of plant material occurred during the Mt. St. Helen’s eruption and flooding by Spirit Lake. (Back to Top)





Starving Dinosaurs



A further point of interest is that in some layers,  supposedly representing millions of years, very few different species can be found.  Often only a handful of different ones are present in a given layer representing thousands or even millions of years.  Sometimes a large species of dinosaur will be found in a particular layer with almost nothing else in the same layer with this large meat-eating dinosaur. 1   What on earth did the dinosaur live on for millions of years? 

Again, consider the Morrison Formation (Late Jurassic) in the western United States. This formation has an average thickness of 100m (300 ft) and extends over 1,000,000 square km (400,000 square mi), being found from Canada to Texas, the Dakotas to Idaho and Arizona to Oklahoma.  It is known as one of the world’s richest sources of dinosaur fossils, but also contains fossil fish, frogs, salamanders, lizards, crocodiles, pterosaurs, dinosaur eggs, and shrew- to rat-sized mammals.  The dinosaur bones occur in the middle green siltstone beds and in the lower sandstones of the Morrison Formation, often in graveyards composed of densely packed bones.  It is commonly said that this vast formation was created by sediments carried by streams and rivers from some ancient highlands into swampy lowland environments.  But how did gentle streams and small intermittent floods pack together so many dinosaur fossils as well as a wide variety of other fossils, without preserving very many plant fossils as well?  It seems like the Morrison Formation is, "practically barren of plant fossils throughout most of its sequence." And yet, some of the preserved remains are from very large plant eating dinosaurs.  For example, the dinosaur Apatosaurus is thought to have consumed about 3 or 4 tons of vegetation on a daily basis.  The relative lack of preserved vegetation makes one wonder how such massive beasts survived in this environment.  Also, fossils within this region show general current orientation.  It seems like such massive and concentrated burial grounds as are found in the Morrison Formation that show current orientation with little or no surrounding vegetation are best explained by a very large and rapid burial/catastrophic flooding event.34,35 (Back to Top)




Headless Dinosaurs



 I will leave you with one last observation.  There is a common saying among scientist that “finding the head of a dinosaur is like finding a needle in a haystack.”2   This is to say that the greatest majority of dinosaur skeletons found have no head attached to their bodies.  There are actually only a dozen or so complete dinosaur skeletons in the entire world.  Many more dinosaur skeletons than this have been found of course, but they are not complete.  Often they are missing their heads.  Why would a dinosaur loose its head if it died a simple death and just fell over on the ground to be buried?  Even scientists admit openly that it appears like most dinosaurs were washed into their current locations by heavy currents.2   A head is not as well attached to the rest of the body as other limbs.  A catastrophic flood could be the reason that there are so many headless dinosaurs around. (Back to Top)





Dinosaur Soft Tissues and Blood






"The lab filled with murmurs of amazement, for I had focused on something inside the vessels that none of us had ever noticed before: tiny round objects, translucent red with a dark center. Then a colleague took one look at them and shouted, 'You've got red blood cells. You've got red blood cells!'.  It was exactly like looking at a slice of modern bone. But, of course, I couldn’t believe it. I said to the lab technician: 'The bones, after all, are 65 million years old. How could blood cells survive that long?'" 10,11,50         

This account was given by Mary Schweitzer, a PhD student at the time, from Montana State University.  A well preserved Tyrannosaurus rex skeleton had been found in 1990 and brought for analysis too Montana State University.  During microscopic examination of the fossilized remains, it was noted that some portions of the long bones had not mineralized, but were in fact original bone.  Upon closer examination it was noted that within the vascular system of this bone were what appeared to be red blood cells (note retained nucleus in the center of the apparent RBCs and the fact that reptiles and bird generally retain the RBC nucleus while mammals, like humans, do not). 50 Of course, this did not seem possible since the survival of intact red blood cells for some 65-million years seems very unlikely if not downright impossible.  

Further testing of these cells was done to attempt to disprove the notion that they could possibly be red blood cells.  Several analytical techniques were used to characterize the material to include nuclear magnetic resonance (NMR), Raman resonance and Raman spectroscopy (RR) and electron spin resonance (ESR).  These techniques did identify the presence of heme group molecules ranging in size from between 5,000 and 30,000 daltons (between 35 to over 200 amino acids in size), but the detection limits of these methods were not able to rule-out or rule-in the presence of hemoglobin or myoglobin proteins due to the small amount of specimen available.   So, Schweitzer and her team decided to use a more sensitive detection method to detect certain very specific types of proteins. They used the immune system of rats.  They injected some of the T. rex extract into laboratory rats to see if these rats would mount an immune response to the foreign T. rex material.  And, the rats did mount a very specific immune response against hemoglobin.  This immune response was not just against hemoglobin in general, but against certain types of hemoglobin.42 The reaction was strongest against pigeon and rabbit hemoglobin with a weak reaction against turkey hemoglobin, but there was no reaction against snake hemoglobin.  The specificity of these reactions were further confirmed by the lack of reactivity with plant and sandstone extracts. 

This is significant since many previous real time studies with protein decay suggest that sizable portions of protein sequences do not remain intact beyond a few tens of thousands of years at best (Fossils, Protein and DNA). Proteins and DNA usually decay very rapidly. Therefore, it would be quite something indeed to find significantly intact hemoglobin after tens of millions of years. Some have even suggested that significantly intact proteins would indicate that such fossils are not in fact tens of millions of years old, but were in fact recently buried within only a few tens of thousands of years at most. 

Consider the conclusions that Schweitzer and her team made concerning these findings: 


"The production of antibodies specific for hemoglobin in two rats injected with the trabecular extract is striking evidence for the presence of hemoglobin-derived peptides in the bone extract. . . That the antisera did not react with snake hemoglobin shows that the reactivity is specific and not artifact. . . When considered as a whole, the results support the hypothesis that heme prosthetic groups and hemoglobin fragments were preserved in the tissues of the Late Cretaceous dinosaur skeleton." 42



These results are quite interesting since they indicate a very specific immune response, not just against hemoglobin, but certain types of hemoglobin molecules. Note again that the antibodies formed did not react against snake hemoglobin indicating that the antibody reactivity was "specific and not artifact." The question is, how much of the original T. rex hemoglobin molecule would need to be intact to elicit such a specific immune response in the laboratory rats?

Schweitzer goes on to suggest that "Immunogenicity is not dependent on fully intact protein, and even very small peptides are immunogenic when complexed with larger organic molecules . . . even after extensive degradation has occurred."42 But how extensively, roughly, could the hemoglobin molecules have degraded and yet retain their ability to elicit a fairly strong and quite specific immune reaction in laboratory rats?  In order to obtain such strongly specific immunogenicity it would seem that a significant percentage of the globin portion of the hemoglobin molecule would need to be intact in at least some of the extracted specimen. In fact, larger molecules were indeed present. Schweitzer proved that there were heme-containing molecules ranging from at least 5,000 to 30,000da in size, and maybe even larger. But, how could a protein of any significant size large enough to elicit an immune response to begin with, as well as a specific immune response observed in this case, be maintained over the course of 65 million years?  One might very reasonably conclude that natural decay, over this amount of time, would completely destroy the ability of hemoglobin or the required larger fragments of degraded hemoglobin from being antigenic much less so specifically antigenic.

The explanation for this phenomenon, given later by Dr. Horner (Schweitzer's boss) and even Schweitzer herself, was that the tougher heme molecule survived the 65 million years with maybe three or four amino acids of the original globin molecules attached to it.  Consider the following statement Schweitzer made in a response to an inquiry by Dr. Jack Debaun:


"But the heme itself is too small to be immunogenic [only about 652 daltons].  We believe that there were possibly 3-4 amino acids from the original protein attached to the heme, and that was what may have spiked the immune response." 43


Now, it just seems quite unlikely that just 3 or 4 amino acids stuck onto a heme group is going to give rise to an immune response at all not to mention a specific immune response for a certain type of hemoglobin as was found in this case (Note that a fully formed globin molecule ranges from 141 to 146 amino acids in length with specific folding characteristics that make up various antigenic "epitopes" that antibodies detect). As far as I have been able to tell, the degree of immune response specificity noted by Schweitzer et al. has never been realized in any confirming experiment with so few hemoglobin amino acids stuck to a heme group (just over 1,000da in size). Even if such an experiment were successful, it certainly doesn't seem like a very likely explanation in this case.  

There are several reasons why I feel this way.  For one thing, a certain minimum antigen size is required before it can elicit an immune response regardless of its structure. The most potent immunogens are macromolecular proteins with molecular weights greater than 100,000da (~740aa - Note: the average amino acid weighs ~135da).  Substances weighing less than 10,000da (~75aa) are only weakly immunogenic, and those foreign proteins/antigens weighing less than 1,000da (~7aa) are usually completely non-immunogenic. Homopolymers (repeats of the same amino acid) are pretty much non-immunogenic regardless of size.  Co-polymers of glutamic acid and lysine must be ~35,000da (~250aa) to be immunogenic.  It seems then that, in general, immunogenicity increases with structural complexity.  Also, aromatic amino acids, such as tyrosine or phenylalanine, contribute much more to immunogenicity than do non-aromatic amino acids.  For example, the addition of tyrosine to a co-polymer made up of glutamate and lysine reduces the size limitation to ~15,000da (~100aa) and adding tyrosine and phenylalanine together reduces the minimum to 4,000da (~30aa).  Also, it is all four levels of protein structure (1o, 2o, 3o, & 4o) that influence immunogenicity - not just a short linear sequence of amino acids.44-47

Of course, a rather specific immune response can be elicited by relatively few amino acids as part of an epitope on a larger protein molecule, but they usually are not immunogenic without first being part of a larger molecule (i.e., "complexed" to a larger molecule before being introduced to the immune competent host).  Also, antigenic epitopes are not usually sequential in nature but are assembled by protein folding (i.e., bringing together amino acids that are widely separated on the protein chain).  This means that a rather large portion of the original molecule usually needs to be intact in order for most epitopes to remain intact.  Epitopes with definite three-dimensional shapes and charged amino acids are particularly well recognized by antibodies. The average epitope probably involves about 7 to 15 contact amino acid residues and a few of these may be critical to the epitope's specificity and the avidity of the antibody-antigen reaction.44-47  But, in order to make an epitope antigenic, it must be processed first.

Antigen presenting cells (APCs) like macrophages, dendritic cells, and even B-cells are responsible for antigen processing and the presentation of epitopes/antigens to the T-cells.  T-cells do not recognize the initial foreign antigen directly.  They only recognize processed parts of antigens, usually consisting of no more than 15 or so amino acids, presented to them by APCs in association with MHC (major histocompatibility) molecules.  So, in order to activate T-cells (required for cellular immunity and very helpful in humoral immunity), the foreign antigen must first be recognized as "foreign" by the APC cells.  This initial APC recognition requires more than just a handful of amino acids floating around or else there would be complete meltdown of the immune system.  In fact, generally speaking, molecules with a molecular weight less than 10,000da (~75aa) are only weakly immunogenic when picked up by APC cells.  Significant potency usually requires antigens to be rather large at over 100,000da (~750aa), or at least above 5,000da (~35aa).48,49 

Given all this, it seems quite difficult for me to imagine how "3 or 4" amino acids stuck to a heme group could elicit an immune response in the first place, not to mention a specific immune response.  Recall that the heme molecule, by itself, only has a molecular weight of around 652da.  To make a strong as well as specific immunogen (such as the immunity developed in rats exposed to T. rex extract in this case) one might expect the immunogenic hemoglobin molecules to be at least 5,000 to 10,000da (~35 to 75aa or so) in size.44-47 Certainly then, a heme group with 3 or 4 amino acids attached to it (just over 1,000da) would not seem to give rise to such an immune response (specific to a certain type of hemoglobin) observed by Schweitzer et al. in rats exposed to T. rex bony extract. 

There are several common arguments used to try and explain these apparent difficulties. One argument is that very small degraded fragments of hemoglobin molecules (3 or 4 amino acids in size) reattached themselves to each other to form new larger molecules with sufficient size to be immunogenic. The problem here is that the rearrangement of so many covalent bonds over the course of some 65 million years would seem to affect not only the inter-amino acid bonds, but the intra-amino acid bonds as well. Of course, such a degree of rearrangement would destroy antigenic epitope specificity. Note also that the heme molecule itself is not bound by covalent bonds to the globin portion of the hemoglobin molecule. It is held in place in a crevice of the globin molecule by many non-covalent bonds that are individually much weaker than the covalent bonds that hold the amino acids together. If the covalent bonds were so commonly broken over time so as to leave only very small chains of 3 or 4 amino acids from the original globin molecule intact, how was the much weaker non-covalent bond between the heme group and a small chain of only 3 or 4 amino acids maintained? It would seem that as the protecting crevice surrounding the heme group was degraded to any significant degree that the non-covalent bonds holding the heme group molecule in place would not have lasted very long. The heme group would have been lost long before the much stronger covalent bonds between amino acids in chains much longer than 3 or 4 amino acids would have been broken.  

Another argument is sometimes used that Schweitzer failed to identify any specific size of hemoglobin fragment by gel electrophoresis.  What happened is that the electrophoretic pattern observed by Schweitzer was a diffuse or smeared pattern.  This means that there were no discrete clusters of proteins that were the same size.  Certainly, this is only to be expected since a wide range of protein sizes would be formed after an extended period of degradation.   The fact of the matter is that hemoglobin fragments ranging between 30 and 200 amino acids in size where definitely present in the T. rex extract (per NMR analysis filtering) and that these molecules were most likely intact fragments of the original T. rex hemoglobin molecules and not reformed molecules made up of tiny fragments.42

 If this is not already enough, Schweitzer recently made an even more startling discovery.  About three years ago (2002) she and her team had to divide a very large T. rex thigh bone in order to transport it on a helicopter. When the bone was opened flexible soft tissue "meat" was found inside. This is incredible because this bone was supposed to be some 68 million years old. Microscopic examination revealed fine delicate blood vessels with what appear to be intact red blood cells and other type of cells like osteocytes - which are bone forming cells. These vessels were still soft, translucent, and flexible. Subsequent examination of other previously excavated T. rex bones from this and other areas have also shown non-fossilized soft tissue preservation in most instances.54   

This find calls into question not only the nature of the fossilization process, but also the age of these fossils. How such soft tissue preservation and detail could be realized after 68 million years is more than miraculous - - It is unbelievable! Schweitzer herself comments that, "We may not really know as much about how fossils are preserved as we think . . .” 54  Now, if that is not an understatement I'm not sure what is.

So, it seems rather clear, despite the objections of many evolutionists, to include Schweitzer herself, that a 1,000da molecule would elicit an extremely weak response at best and would not necessarily elicit a specific response to a certain type of hemoglobin molecule since surface epitopes are generally more specific in their antigenic nature than are buried epitopes (i.e., heme is somewhat hidden within a cleft of the hemoglobin molecule so 3 or 4 amino acids attached to it would also be somewhat hidden). How then is it remotely logical to suggest that a molecule weighing just over 1,000da (a heme group plus 3 or 4 amino acids) could elicit such a strong as well as specific immune response as Schweitzer et al. observed?  In light of the additional recent finds of even more striking soft tissue and blood cell preservation, it seems much more likely that such an immune response so specific for certain types of hemoglobin could only be elicited by a larger portion of intact hemoglobin than many scientists seem to even consider.  Of course, one can't really blame them because explaining how delicate soft tissue vessels (with obvious red blood cells inside containing relatively large portions of hemoglobin molecules) could remain intact for over 65 million years seems just a little bit difficult. 

Such finds are much more consistent with a fairly recent catastrophic burial within just a few thousand years of time. Non-catastrophic burial would allow for rapid biodegradation of such delicate soft tissues. Time itself destroys soft tissues as well as DNA and proteins in short order.  Current real-time observations suggest that bio-proteins could not remain intact more than a few tens of thousands of years - 100,000 years at the very outside limit of protein decay.  The fact that such proteins are found, intact, in bones supposedly older than 65 million years is simply inconsistent with such an assumed age - by many orders of magnitude. (Back to Top)








So, where does the evidence put us?  What position seems most reasonable?  What theory answers the most questions?  Do fossils and the geologic column that contains them represent millions of years of slow sedimentation or do they reveal a time of huge catastrophe and rapid deposition, death, and burial on a global scale? (Back to Top)



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  42. Mary H. Schweitzer,* Mark Marshall, Keith Carron, D. Scott Bohle, Scott C. Busse, Ernst V. Arnold, Darlene Barnard, J. R. Horner*, and Jean R. Starkey,  Heme compounds in dinosaur trabecular bone,  Proc. Natl. Acad. Sci. USA, Evolution, Vol. 94, pp. 6291-6296, June 1997 ( )

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. Home Page                                                                           . Truth, the Scientific Method, and Evolution   

. Methinks it is Like a Weasel                                                 . The Cat and the Hat - The Evolution of Code   

. Maquiziliducks - The Language of Evolution             . Defining Evolution    

. The God of the Gaps                                                           . Rube Goldberg Machines  

. Evolving the Irreducible                                                     . Gregor Mendel  

. Natural Selection                                                                  . Computer Evolution  

. The Chicken or the Egg                                                         . Antibiotic Resistance  

. The Immune System                                                            . Pseudogenes  

. Genetic Phylogeny                                                                . Fossils and DNA  

. DNA Mutation Rates                                                            . Donkeys, Horses, Mules and Evolution  

. The Fossil Record                                                                . The Geologic Column  

.  Early Man                                                                                . The Human Eye  

. Carbon 14 and Tree Ring Dating                                     . Radiometric Dating  

 . Amino Acid Racemization Dating                   . The Steppingstone Problem

.  Quotes from Scientists                                                           . Ancient Ice

 . Meaningful Information                                                          . The Flagellum

 . Harlen Bretz                                                                           


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Stacking the Deck


God of the Gaps


The Density of Beneficial Functions


All Functions are Irreducibly Complex


Ladder of Complexity


Chaos and Complexity


Confusing Chaos with Complexity


Evolving Bacteria


Irreducible Complexity


Scientific Theory of Intelligent Design


A Circle Within a Circle


Crop Circles


Mindless vs. Mindful


Single Protein Functions


BCR/ABL Chimeric Protein


Function Flexibility


The Limits of Functional Flexibility


Functions based on Deregulation


Neandertal DNA


Human/Chimp phylogenies




The Geologic Column


Fish Fossils


Matters of Faith


Evidence of Things Unseen


The Two Impossible Options




Links to Design, Creation, and Evolution Websites





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