"the global biostratigraphic column seems to be real." — Kurt Wise and Donna Richardson, 2023, two young-earth creationists, after testing 114 stratigraphic boundaries in the Paleobiology Database.1
"Creationists therefore need to accept this fact. It certainly CANNOT be said that traditional creation theory expected (predicted) any of these fossil finds." — Kurt Wise, 1995, on the transitional series between larger groups.2
"We conclude that some unspecified process of bounded evolution is responsible for the band we observe in our data (Fig. 1)." — Josef Uyeda and three colleagues, 2011, on why body size stops diverging over long spans.3
Summary
The fossil record is the one body of evidence in which the history of life and the history of the rocks can be read side by side. This section asks what it shows, and which of the claims made about it by young-earth creationists and by their critics survive a check against the rocks, the databases and the sources. It has twenty-six articles in six groups. Every one of them works from the order of the rock alone: what lies above what in one section, and how sections line up by their fossils, both of which young-earth geology accepts. No radiometric date is used as evidence anywhere in the section.
The section's verdict, stated first: the fossils lie in a real, worldwide order, and the young-earth side does not yet have a model that explains it. The order is measured across two million catalogued finds, and no claimed exception has survived an audit. The named transitional sequences are real and run in that order. Four of them, reptile to mammal, fish to four-limbed animal, land mammal to whale, and dinosaur to bird, cross the line young-earth biology itself draws around a created kind. Every claimed out-of-place fossil examined on this site fails, and the absence of any pre-Flood human bone or worked stone from Flood rock is the hardest single fact in the section.
Several young-earth claims survive, in narrower forms than they are usually given. The spectacular fossils were buried fast, and the excavators agree. Gut contents and healed bites cost a one-year Flood nothing. Protein and flexible tissue in dinosaur bone outlast measured decay rates by orders of magnitude, and no mechanism has been shown to preserve them for longer than two years in a laboratory. Change in fossil lineages stays inside bounds that nobody has explained. Skeletons alone are a poor guide to ancestry. Many living groups keep their body plans at the rank of family through most of the column. And the specialists on the Cambrian explosion say in print that no proposed cause is sufficient to explain the origin of the animal body plans.
Much is unfinished on both sides. On the young-earth side: the four cross-family sequences, stacked track horizons, bones bored where they lie, the rebuilding of sea-floor life after the mass extinctions, and the proposal that the pre-Flood continent was subducted. On the mainstream side: how soft tissue survives, what holds change inside bounds, and what caused the Cambrian body plans.
One pattern runs through all six groups. Where young-earth claims succeed, they succeed about particular fossils or about what fossils cannot show: a fish sealed fast, a protein that outlasted its clock, a skeleton that cannot place itself in a tree. Where they fail, they fail on patterns measured across the whole column: the order, the sequences, the nesting horizons, the recoveries above the extinctions. The young-earth side's best corrections came from its own scientists: Kurt Wise in 1995 and 2023, John Morris on the Paluxy tracks in 1986, Paul Garner on dinosaur nests in 1996, and Warren Johns on Precambrian pollen in 2022.
The six groups under this heading:
- Reading the Record. The record reads well for order and for comparisons, and poorly for completeness, single absences, ancestry from shape and restored soft parts. No young-earth model reproduces the order. Rapid burial is right for spectacular fossils and wrong for the rocks, fraud discredits nothing, and dinosaur soft tissue is an unsolved problem for deep time.
- Transitional Sequences. The named sequences are real and run in stratigraphic order, and the flat claim that there are no transitional forms is dead. The horse series stays inside one family and costs creationism nothing. The four that cross the family line are an unsolved problem for the young-earth model.
- The Cambrian Explosion. The explosion is real, and burrows show it is more than a change in what could fossilise. But Ediacaran animals and Cambrian stem groups refute the claim that all phyla appeared at once with no intermediates, and the one phylum-level example in Wise's 1995 list is misattributed.
- Stasis, Extinction, and Evolutionary Tempo. Stasis, living fossils and mass extinctions are all real, and none decides between the models alone. Deep time has too little change for its time, and a young earth too much change for its time. The reading of mass extinctions as burial order fails, and the reading in which the Flood did the killing is unfinished.
- Trace Fossils. Michael Oard's model of briefly exposed Flood sediments fits every surface that needed a day or less, and every trace whose clock ran inside a living animal. It fails for nests, where one embryo's teeth count 99 days against an 80-day window. Stacked track horizons and bored bones are unfinished.
- Claimed Fossil Anomalies. No claimed human track, tool, pollen grain or living dinosaur survives four tests: provenance, context, independent identification and open publication. Creationists killed many of these claims themselves.
The earliest hominins, from Sahelanthropus to Lucy, were first planned for this section. They are now argued under Human Origins and Genetics, and the last section of this page points to them.
How the section judges the evidence
Order, never dates. Every argument in the section rests on relative order. Within one stack of undisturbed rock that is superposition: the higher layer came later. Between basins and continents it is the matching of rock by its fossils, a method older than radiometric dating that does not depend on it. William Smith identified the strata of England by their fossils in 1816, and Albert Oppel matched ammonite zones across England, France and Germany in 1856 to 1858.45 Young-earth geologists accept both. Kurt Wise and Donna Richardson tested 114 boundaries in the Paleobiology Database in 2023 and concluded that "the global biostratigraphic column seems to be real."11 So fossil order matched between continents is open to both sides, and the section applies that evenly: to the whale and synapsid sequences and the Cambrian count, and to the bird "temporal paradox" and the Polish trackways that young-earth writers cite. Each of those stands or falls on its evidence. The one writer who cannot use them is the one who calls the fossil column circular, because they are its output. What no argument here rests on is an age or a duration in years. Where an age in millions of years appears on these pages, it is the mainstream figure under discussion, not something the reader is asked to accept.
Name the rank. Young-earth biology accepts descent with change inside a created kind, and its own journal puts the kind "at or near the taxonomic level of family."6 So a sequence inside one family costs creationism nothing, and a sequence that crosses several ranks costs a great deal. Every sequence article states the rank its sequence spans.
Compute, then quote, and price every absence. The fossil record is the most quote-mined subject in apologetics, so the articles count instead. They query the Paleobiology Database, a public catalogue of published fossil finds, and they measure its biases before using it.7 They also treat absence as evidence only in proportion to how many fossils were expected. Of the well-sampled fossil genera, 75.9% vanish from the record for at least one stage and then come back.8 An absence counts when the missing thing is durable, well sampled and expected in large numbers.
Three verdicts, not two. A young-earth argument can be wrong. It can be right or partly right. Or the question can be unfinished: the pattern is real, the standard answers fail, and nobody has a working model yet. The section reaches all three, and in two places, soft tissue and the bound on change, the unfinished problem sits on the mainstream side. A series in which every argument failed conveniently for one side would not deserve belief.
Part 1: Reading the Record
Reading the Record gathers six articles on what the record can carry as evidence once its biases are allowed for. Its answer is that the record reads well for order and for comparisons between groups, and poorly for almost everything absolute.
Order goes against the young-earth argument. The Order of the Fossil Record ran 24 boundary tests across the whole database and audited 29 claimed or apparent exceptions. The only fossils found below a group's first appearance were two filing errors: a lungfish filed under the reptiles, and a sponge bound to an insect's name.7 Hydrodynamic sorting, escape ability, ecological zonation and the published Flood models do not reproduce the order. The hardest single fact is human: the database holds 1,345,826 occurrences below the Neogene and no human bone among them, and no worked stone has been found in place in that rock.910 The Institute for Creation Research grants the first half: "Although we know of no undisputed human skeletal remains in Flood rocks, a few unique artifacts may have come from pre-Flood humans."1111 One young-earth prediction is confirmed, a succession from marine to land fossils up the column.
The other five come out differently. Trends in the Fossil Record is mixed: stasis is real but weaker than claimed, convergence shows that skeletons are a poor guide to ancestry, and the claim that the record is complete enough to make its gaps real fails on measurement. Fossil Preservation finds rapid burial right for the spectacular fossils creationists cite and wrong as a fact about the rocks, since most fossils are shells mixed over centuries and each famous bed is a stack of small burials. Dinosaur Soft Tissue finds the tissue real and original, as even the old-earth biochemist Fazale Rana grants, and finds that the mainstream's iron cross-linking mechanism has not been shown to work for longer than about two years.1212 The radiocarbon dates and "dinosaur DNA" claims fail. Fossil Reconstruction and Fraud finds that scientists caught every famous fraud, so fraud discredits nothing, while the real question about any restoration, which parts are bone, is one the mainstream raised first. How Complete Is the Fossil Record? finds that completeness depends on the group: absences among durable sea animals at genus and family rank are evidence, absences among insects, soft-bodied animals and most land vertebrates prove little, and the claim that the record is complete enough to make its gaps real holds only in that narrow form.
Part 2: Transitional Sequences
Transitional Sequences takes the six best-known named sequences one at a time and asks two questions of each. Is the sequence real, or a museum line-up? And does it cross a line young-earth biology draws?
The sequences are real. Each runs in the order the rock gives, and the flat claim that there are no transitional forms fails in all six articles. None is a ladder of ancestors either. Every one turns out to be a bush of side branches and late survivors with real gaps, and the mainstream specialists said so first.
Rank decides what each costs. The Horse Series stays inside the family Equidae, and three creationists called the fossil horses one created kind in the title of a 2003 paper.13 The Reptile Jaw and the Mammal Ear, Tiktaalik and the Fish-to-Tetrapod Transition, Whales and the Land-to-Sea Transition and Archaeopteryx and the Origin of Birds all cross the family line by several ranks. Wise saw this in 1995. He wrote that common intermediates between species "has been the most disappointing for classical Darwinists," listed the higher-level series as confirmed, and concluded: "Creationists therefore need to accept this fact."222 The Missing Transitions is mixed: the turtle gap and Romer's Gap have closed, while bats and pterosaurs keep narrower gaps at the origin of the wing.
So the young-earth position on the four cross-family sequences is unfinished. Every published objection fails, and no young-earth model predicts why anatomy and rock line up. The hub adds that the longer this stays so, the more it counts against the model. The live lines are narrow: the boundary between the Mesozoic bird-like animals and modern birds, the bat and pterosaur wings, the thin early records of whales and of four-limbed animals, and Wise's untested suggestion that the early whales were several created kinds.
Part 3: The Cambrian Explosion
The Cambrian Explosion asks whether the sudden appearance of animal body plans near the base of the Cambrian is real, how large it is, and which claims about it survive a check against the sources.
The pattern is real, and burrows show it. Shells and skeletons can be answered with "this is when animals became easy to fossilise." Burrows cannot, because they have no hard parts. Across the Ediacaran–Cambrian boundary the number of trace-fossil types rises from 7 to 42, their basic designs from 5 to 22, and burrowing depth goes from about a centimetre to a metre by the second Cambrian stage.1414 The ichnologists who compiled those figures conclude that "Trace-fossil information strongly supports the Cambrian explosion."14 The article's own database count finds that first appearances at the rank of phylum and class bunch into the lower Cambrian, while lower ranks keep appearing. And the specialists report in print that no proposed cause is sufficient to explain the body plans.
But the strong young-earth claims fail. "All the animal phyla appear at once" is dead: ten phyla in the database first appear later, and seven living phyla have no fossil record at all. The Ediacaran rocks below hold animals, including Kimberella, found with the scratch marks it made while feeding. The figure of "5 to 10 million years" is dead, because it misreports the mainstream's own timescale. The strongest recent measurement of animal form, by Bradley Deline and colleagues, concludes that the gaps between living groups are "a consequence of the extinction of phylogenetic intermediates."1515 And the only phylum-level example in Wise's 1995 list, Pikaia "between echinoderms and chordates," is misattributed: the Gould pages he cites call it "a chordate, a member of our own phylum."16162 So Wise's concession has no surviving entry above the class.
The verdict is mixed. The event is real and poorly explained, and the article declines to turn "poorly explained" into an argument for design. The young-earth slogans about it are wrong. The article's own timing result carries an open confound: a global anoxic extinction in the middle of the Cambrian, the Sinsk Event, sits almost exactly where the count of new phyla stops, and nobody has tested whether one caused the other.
Part 4: Stasis, Extinction, and Evolutionary Tempo
Stasis, Extinction, and Evolutionary Tempo asks what the record says about the pace of change. It treats stasis and punctuated equilibrium, which are argued in Part 1 of the trends article, beside Living Fossils and Mass Extinctions.
All three patterns are real, and each has been oversold. Most fossil lineages wander rather than stand still. Most "unchanged" living fossils are unchanged only at the rank of family, and at the rank of species only ginkgo leaves carry a living species into Mesozoic rock. The largest extinction, at the end of the Permian, killed about 81% of marine species, not the 90 to 96% often quoted.1717
None of the three decides between the models, but each sets a cost. Deep time has too little change for its time. Change measured over years is fast, yet over millions of years it stays inside bounds, and the authors of one of the studies that measured this call the cause "some unspecified process of bounded evolution."33 A young earth has too much change for its time. Its own biologists need "a massive burst of speciation" in "just a few hundred years" after the Flood, and call explaining it "the most challenging explanatory task" their model faces.1818
On mass extinctions the young-earth position is split, and the stronger half is unfinished. The Institute for Creation Research reads the extinction levels as "major shifts in the burial pattern of fossils during the Flood."1919 That reading predicts thousands of later fossils of the vanished groups, and they are not there. The other reading, that the Flood did the killing, survives that test. But every active young-earth model puts the end-Permian extinction inside the Flood, and above it lies an ordered recovery: dwarfed shells, missing reefs, and at Guizhou in China a reef about 900 m thick whose builders arrive in sequence.2020 On ICR's own timetable that reef had at most 50 days.21 No young-earth author has attempted the recovery.
Part 5: Trace Fossils
Trace Fossils gathers four articles on footprints, nests, dung, bites and borings, each made by an animal alive on a particular surface. If that surface lies in Flood rock, the ground was firm and the water gone while the Flood was under way. The one young-earth model for all of them is Michael Oard's Briefly Exposed Diluvial Sediments, BEDS for short, which puts the eggs and tracks "between Day 40 and about Day 120 of the Flood."2222
Fast burial is agreed, and it does not decide the question. Every track surface, clutch and dung pile in these articles was buried fast, and the excavators say so, reading most of them as local floods. What decides the question is how long each surface lasted before burial, and how many surfaces one place holds.
The verdicts depend on where each trace's clock ran. Gut contents, healed bites and shipworm-bored driftwood ran their clocks inside a living animal or in seawater, so they cost the Flood year nothing. Fossil Tracks and Trackways and Coprolites, Gut Contents, and Feeding Traces find that BEDS fits every surface that needed a day or less. Fossil Nests and Eggs finds that it fails for nests. The daily growth lines in the teeth of a Hypacrosaurus embryo from Devil's Coulee, Alberta, give "a value of 99.45 d," and 171 days with the time before the teeth formed, against Oard's window of about 80 days.2323 Briefly Exposed Diluvial Sediments adds the bills up. It leaves stacks of a hundred or more track horizons, and bones bored by beetles or worms where they lie, unfinished.
A young-earth geologist stated the nest problem first. Paul Garner wrote in 1996 that nests on successive horizons "stretch Oard's Flood chronology beyond breaking point," and moved the end of the Flood below the Triassic.242424 But in 2000 Garner and his three co-authors wrote that none of them was satisfied with the model they had proposed in 1996, as the issues below explain. So no active young-earth camp holds the low-boundary escape. The only other escape in print, that the mothers held their eggs for most of the incubation, has no living bird or crocodile to support it.
Part 6: Claimed Fossil Anomalies
Claimed Fossil Anomalies sets out four tests for a fossil said to be out of place: where it was found and who can show it, whether it is part of the rock, whether someone who does not need the result identified it, and whether it was published where critics can answer. It lists more than forty such claims across thirteen articles, with what each young-earth organisation says about them today.
Every claim fails, and most fail at the first test. Human and Dinosaur Tracks Together shows that the Paluxy "man tracks" were 1930s carvings, erosion marks and long dinosaur tracks whose toes had been filled in. ICR withdrew them in 1986: "it would now be improper for creationists to continue to use the Paluxy data as evidence against evolution."2525 Dinosaurs in Ancient Art and Text finds the Ica stones and Acámbaro figurines modern and the rock-art dinosaurs composites and stains. Living Dinosaur Claims finds forty-five years of searches that returned testimony and blurred pictures but never a body. The hub itself tests the Precambrian pollen of the Roraima rocks, which leans strongly to contamination, as a creationist review in Creation Ministries International's own journal concluded in 2022.2626
The organisations have retired these claims unevenly, and their own researchers did much of the work. The one real anomaly in the register is of another kind: soft tissue in dinosaur bone, a preservation puzzle in fossils whose place in the rock is not in doubt. None of this refutes the belief that people and dinosaurs once lived at the same time, which rests on Genesis. It does mean that the record has not supplied one verified object out of place.
Part 7: The section side by side
"Verdict" uses the three kinds named above and says whose claim it judges. "Where argued" names the article that carries the evidence.
| Question | Where argued | Verdict | Strongest point for the mainstream | Strongest point for the young-earth side |
|---|---|---|---|---|
| Does a one-year Flood explain the global order of fossils? | The Order of the Fossil Record | Against the young-earth argument | All 29 claimed or apparent violations fail; no human bone or worked stone among 1,345,826 occurrences below the Neogene | The marine-to-land succession up the column is confirmed; the subducted-continent answer is untested rather than refuted |
| Is the record complete enough to make its gaps real? | Trends in the Fossil Record | Against: completeness fails on measurement | Three quarters of well-sampled genera have holes in their own ranges | Abrupt appearance at family rank holds in durable groups with nearly full records |
| Do fossils show the rocks were laid down in a catastrophe? | Fossil Preservation | Partly right: right for single fossils, wrong for the rocks | Most fossils are shells mixed over centuries; one Burgess bed holds 26 separate burials | Articulated and soft-bodied fossils needed sealing within hours to weeks |
| Can original protein last tens of millions of years? | Dinosaur Soft Tissue | Partly right; the deep-time explanation is unfinished | Iron from blood stabilised tissue more than 200-fold; the radiocarbon and DNA claims fail | No preservation mechanism has been tested past two years |
| Do frauds and restorations discredit paleontology? | Fossil Reconstruction and Fraud | Wrong about fraud; right, and mainstream, about restorations | Scientists caught every fraud | A restoration can triple a dinosaur's mass; ask which parts are bone |
| Are there transitional sequences? | Transitional Sequences | Against the young-earth argument | Rock order and anatomy order agree in all six; the jaw-to-ear change was predicted from embryos in 1837 | The museum ladders are wrong, and the horse series fits one created kind |
| Do the cross-family sequences have a young-earth explanation? | The jaw, fish, whale and bird articles | Unfinished | Four sequences cross the family line by several ranks, and Wise conceded them in 1995 | The early whale and tetrapod records are thin, and Wise's several-kinds escape for whales is untested |
| Did all the animal phyla appear at once? | The Cambrian Explosion | Wrong; the explosion itself is real and unexplained | Ediacaran animals, stem groups, ten later phyla | Burrows show a real jump; specialists report no sufficient cause |
| Does stasis favour creation? | Trends, Part 1 | Neither side: real, and weaker than claimed | Measured short-term rates are fast; directional change is documented | The bound on long-term change has no accepted explanation |
| Are living fossils unchanged? | Living Fossils | Right at family rank; wrong at genus and species, except ginkgo | Living genera are young or have no fossils | Family-level conservatism is conceded in print |
| Were mass extinctions only burial order, and does the Flood explain the recoveries? | Mass Extinctions | Burial order: wrong. Flood killing: unfinished | An ordered recovery, including a 900 m reef built in sequence, follows each kill | Sudden losses within centimetres fit a catastrophe |
| Do trace fossils fit a few months of exposure inside the Flood? | Trace Fossils | Fits single surfaces; unfinished for stacks and bored bones; fails for nests | 99 counted days of embryo growth against an 80-day window | Gut contents, healed bites and single track surfaces cost the Flood nothing |
| Is there a fossil out of place? | Claimed Fossil Anomalies | Wrong | No claim survives provenance, context, identification and publication | Young-earth researchers did much of the testing themselves |
Three things stand out. The verdicts differ, as they should if the evidence is being followed. The young-earth side's strongest points are almost all about single fossils, or about how thin and branched the record is. And the one large-scale result that survives every bias the section measured, the order, is the one that goes against the young-earth side.
Part 8: What the section adds up to
- Single fossils favour the young-earth side; patterns across the column favour the mainstream. A fish sealed within days, a stomach still full, a vessel that outlasted its decay clock and a nest buried by a flood are all true facts about one specimen. None of them says when the rock was laid down or why one group lies above another. The order, the sequences, the stacked nesting horizons and the recoveries above the extinctions are measured across many sections, and those are where the young-earth model has no answer yet.
- Absence must be priced, and the rule binds both sides. The coelacanth vanished from rock that should hold dozens of its fossils, and lived. So a missing intermediate is weak evidence that none existed, and a missing ancestor below a Cambrian phylum is weak evidence that none lived. The same rule binds the mainstream when it explains away a missing intermediate. But absence counts when the missing thing is durable, well sampled and expected in large numbers. Worked stone from a city-building pre-Flood people is all three, and it is missing from 1,345,826 occurrences of other fossils.9
- Several costs meet at the Flood/post-Flood boundary, and the active camps carry all of them. A boundary below the Triassic would relieve the nests, the Mesozoic track stacks and the Early Triassic recovery at once, by putting them after the Flood. But it gives up most of the fossil record that other Flood models assign to the Flood, and the four British creationists who proposed it in 1996 wrote in 2000 that none of them was satisfied with it.2727 Every active young-earth camp ends the Flood at or above the end of the Cretaceous. On those placements the nests, the track stacks and the rebuilding of the sea floor after the end-Permian all have to fit inside the Flood year. ICR moves some of the load the other way, suggesting that some Cenozoic track layers "have been misidentified and should be Pleistocene (post-Flood)."19 The Flood/Post-Flood Boundary article weighs the placements, and no single placement has yet been priced against all of these sections at once.
- The flat claims are dead, and the narrow claims are where the work is. "No transitional forms," "all phyla at once," "fossils are frauds," Paluxy and living dinosaurs fail on the evidence, and young-earth organisations have retired several of them. What survives is narrower: the bound on change, the abrupt appearance of durable groups at family rank, the soft-tissue clock, the bird boundary at the end of the Cretaceous, the bat and pterosaur wings.
- Errors ran both ways, but this project's own young-earth sources erred in one direction. The mainstream corrected its own Brasilodon, Casineria and whale reconstructions, and Gene Hunt withdrew his own plankton result. The quotation audit of this project's research notes found that every passage cut so as to change its meaning was cut toward the young-earth argument. The movement's best moments are corrections of its own: Morris on Paluxy, Chadwick on Grand Canyon pollen, Garner on nests, Johns on Precambrian pollen, and Wise and Richardson on the column.
- Both sides owe work, and the lists are specific. The young-earth side needs a Flood model that predicts the order and the cross-family sequences as numbers, with conditions that would show it wrong; a water-level curve for one named section with the exposures matched to its traces; an account of the Early Triassic recovery; baraminology run on the early whales and on the birds on both sides of the end-Cretaceous boundary; a defended pre-Flood population; and the buoyancy arithmetic for a subducted continent. The mainstream owes a soft-tissue mechanism shown to work for longer than two years, a cause for the bound on change, a cause for the Cambrian body plans, and a test of whether the Sinsk extinction ended the Cambrian count.
Objections and responses
These objections cut across the section. Each child article answers the objections specific to its own evidence.
- "The fossil record is the record of the Flood, so of course it shows rapid burial everywhere." Rapid burial is everywhere that spectacular fossils are, and the mainstream agrees. It is not the rule for most fossils, and the spectacular beds are each many small burials. More to the point, rapid burial is the wrong test. A one-year Flood has to explain which fossils lie above which, worldwide, and how many separate living surfaces one section holds. Those are the questions the section's young-earth verdicts turn on, and fast burial answers neither.
- "All of this assumes millions of years." It does not. The order, the sequences, the gap pricing, the trace stacks and the recoveries all use only what lies above what. The young-earth side's own best geologists accept the column as a relative time scale. Wise and Richardson add that index fossils "provide no more information about earth history than a relative time scale."1 A relative time scale is all these articles use. No argument rests on a duration in years; where one is printed, it is the mainstream's figure, attributed to it.
- "A young-earth site that rules against Flood geology this often has given up." Wise ruled the same way in a creationist journal in 1995, and Wise and Richardson did again in 2023. The section's verdicts also go the other way where the evidence does: soft tissue, the bound on change, gut contents, the horse series, family-level conservatism and the unexplained Cambrian body plans. An unsolved problem is not a refutation of creation. But it is not answered by repeating arguments the movement's own scientists have already set aside.
- From the skeptic: "'Unfinished' is a polite word for 'refuted.'" Not quite. A refutation would show that no young-earth account could fit the pattern. The articles show something narrower: every published answer fails, and no model that predicts the pattern has been built. But time counts. Wise named the whale problem in 1995, and the one escape still open has grown weaker since without being tested. A problem that stays open while the evidence against each escape grows is evidence against the model, and the section counts it that way.
- "The gaps between kinds are the real evidence, and they are everywhere." Gaps are everywhere, and that is the difficulty. Three quarters of well-sampled genera have holes inside their own ranges, so a gap alone shows little.8 The gaps that carry weight are narrow and specific: the bat and pterosaur wing, the birds across the end-Cretaceous, the origin of the Cambrian body plans. A young-earth writer who uses the coelacanth's return as a caution has to apply the same caution to missing intermediates.
- "Dinosaur soft tissue shows the bones are young, so the rest of the section falls." It does not. The order is relative, so it needs a burial mechanism whatever the age of the bones, and none of the published ones works. The soft-tissue article treats the tissue as a real anomaly for deep time and a live question, not a date, because its decay clocks are themselves extrapolated from heated bone and young bones.
- "Move the Flood/post-Flood boundary and the problems go away." The placements trade costs, as Part 8 shows. A low boundary, below the Triassic, relieves the nests, the Mesozoic tracks and the Early Triassic recovery, but gives up most of the fossil record other Flood models assign to the Flood, and its own authors wrote in 2000 that none of them was satisfied with it. Every placement an active camp holds keeps the end-Permian extinction in the Flood, and leaves the nests and the ordered recovery to fit inside the Flood year. A placement that works for one article has to be priced against the others.
- "The mainstream has open problems too." It does, and the section prints them: no mechanism for soft tissue past two years, an "unspecified process" holding change inside bounds, no sufficient cause for the Cambrian body plans, and an untested extinction in the middle of the Cambrian count. None of them is about the order of the fossils or the existence of the sequences, which is where the young-earth problems lie. An open problem on one side does not close one on the other.
Issues and unanswered questions
- No young-earth model reproduces the order or predicts the sequences. This is the central gap in the section, and it is on the young-earth side. Wise's 1995 suggestion, that the class-level series were animals of the boundary zones between pre-Flood habitats, has never been turned into a model with numbers and conditions that could show it wrong. The subducted pre-Flood continent, the best answer to the missing pre-Flood world, has a mechanism and a prediction, an accretionary wedge holding the lost continent's debris, but nobody has worked the buoyancy arithmetic or searched the wedge. The pre-Flood population, which would price the missing human remains, has no defended estimate.
- The child articles price the Flood against different end points. The nests and trace articles cite Garner's 1996 placement of the boundary below the Triassic as a live escape, and the Trace Fossils hub says the young-earth organisations publish it beside its rivals. The Mass Extinctions article records that its authors wrote in 2000, "None of us is satisfied with the model that we proposed in 1996," and that no active camp now ends the Flood below the Cretaceous.27 The letter says so in those words, and adds that their thinking had moved on. This page follows the 2000 letter: the low-boundary escape is in print but held by no active camp. The nest verdict does not change, since the trace articles already priced it as a costly escape.
- Whether Kurt Wise took his doctorate under Stephen Jay Gould. The fish, horse, whale and trends articles say he did. The jaw-to-ear article notes that Wise's 1995 paper names only his Harvard degrees, and leaves the supervisor unsourced. This page relies only on the degrees. A series-wide decision is still needed.
- Whether stasis and convergence get articles of their own. Stasis and punctuated equilibrium are argued in Part 1 of the trends article, and convergence in its Part 3, rather than as children of the hubs that summarise them. A proposal to split them out, and another to give the trilobite eye its own article, have not been approved. Until they are, the Stasis, Extinction, and Evolutionary Tempo hub summarises trends Part 1 and links there.
- Work nobody has done, on the young-earth side. A water-level curve for one named section, with its exposures matched to its traces. A whole-column count of track, nest, dung, burrow and soil horizons at one place, such as the Colorado Plateau. An account of the Early Triassic recovery. Baraminology of the early whales and of the birds across the end-Cretaceous, by methods that answer the 2021 criticism from a creationist statistician that such methods "ought to be abandoned."2828 Clarey's database of nearly 3,000 rock columns, which has not been released.
- Work nobody has done, on the mainstream side. A soft-tissue preservation experiment that runs long enough to fit a decay curve. A cause for the bound on long-term change. A lineage-by-lineage test of whether the Sinsk extinction, rather than the end of a radiation, stops the Cambrian count. Fresh cores from the Roraima hornfels, processed under contamination controls, would also settle the last Precambrian pollen claim either way.
- Where this page departs from a child. The order article prints "1.2 million" occurrences below the Neogene in parts of its section on the missing human dead, a figure left from an incomplete download; its own tables give 1,345,826, which this page uses. The trends article's description says the creationist case survives most clearly on stasis and gaps, while the stasis hub finds stasis neutral; their verdict paragraphs agree, and this page follows them.
Verdict
The fossil record is a real, ordered sequence, and it reads that way on relative order alone. Which fossils lie above which is measured across two million catalogued finds, survives every bias the section could measure, and is accepted by the young-earth side's own best geologists. The named transitional sequences run in that order. Four of them cross the line young-earth biology draws around a created kind, and a young-earth paleontologist conceded them in 1995. No claimed out-of-place fossil survives the tests. No published young-earth model reproduces the order, predicts the sequences, fits the stacked nesting horizons into the Flood year, or rebuilds the sea floor after the end-Permian extinction in weeks. On those questions the evidence counts against the young-earth case, and the longer they stay open the more it counts.
The young-earth side is right about more than its critics usually allow. The spectacular fossils were buried fast. Gut contents and healed bites cost the Flood nothing. Dinosaur soft tissue is a real anomaly that the mainstream has not explained. Change in fossil lineages stays inside bounds that its own specialists call "some unspecified process." Skeletons are a poor guide to ancestry, many groups keep their body plans at family rank, and the specialists find no sufficient cause for the Cambrian body plans. None of these dates the rocks, and none touches the order.
The arguments to retire are the ones the section killed: no transitional forms, all phyla at once, the record complete enough to make its gaps real, fraud as proof that paleontology cannot be trusted, mass extinctions as mere burial order, Paluxy, Precambrian pollen and living dinosaurs. The arguments worth working are the open ones: a Flood model that predicts the order as numbers, the subducted continent, the bird boundary at the end of the Cretaceous, the bat and pterosaur wings, the baraminology of the early whales, a water-level curve for BEDS, and a soft-tissue experiment long enough to settle the clock.
The earliest hominins
The fossils older than the genus Homo were first planned for this section, because they are judged on anatomy and position in the rock, as everything here is. They are now argued under Human Origins and Genetics, beside the rest of the hominin fossils.
- Hominin Fossils, the hub for every hominin fossil, finds that the young-earth division of the fossils into apes and humans holds at both ends and splits on the small-brained mosaic fossils between.
- Lucy and the Pre-Human Hominins finds that Lucy was not human, though she walked upright, and that the oldest biped claims rest on few, reconstructed bones. Its five children are Lucy and Australopithecus afarensis, The South African Australopiths, Australopithecus sediba, Paranthropus, and Sahelanthropus, Orrorin, and Ardipithecus.
- Brain Size and the Order of the Fossils applies this section's method to the hominins: brain size rises with fossil date, and young-earth writers accept the order but have not explained it.
Related articles
- The Flood/Post-Flood Boundary, on where the Flood ends in the rock and what each placement costs.
- Geological Claims to Retire, on the coal artifacts, Castenedolo, Calaveras and other claims outside this section.
- Radiocarbon Dating, on carbon-14 in old material, including dinosaur bone.
- Bioturbation and Trace Fossils, on marine burrows and how long a burrowed sea floor takes to form.
Sources
- 1.
Wise, Kurt P., and Donna Richardson. “What Biostratigraphic Continuity Suggests about Earth History.” Proceedings of the Ninth International Conference on Creationism 9:611–625. 2023. A paper by Kurt Wise, a young-earth creationist with a Harvard paleontology doctorate, and Donna Richardson, doing original quantitative work on the same open database the order article uses. Their method: at each of 114 globally defined stratigraphic boundaries they computed the number of local stage-straddling species (NLSSS), meaning species occurring in the stage immediately below and immediately above a boundary within two degrees of latitude and longitude of each other, using the Paleobiology Database, a public fossil database, and they checked the counts at 1°, 3° and 4°. The order article calls it the strongest recent concession from inside the creationist movement, and recomputes its statistic in its Part 6 because the pre-Flood/Flood use does not survive. ↩
- 1a.
Page 623, right column: “the global biostratigraphic column seems to be real.” Their conclusion on the column itself. ↩ ↩
- 1b.
Page 611, section Abstract: “provide no more information about earth history than a relative time scale.” The subject of the sentence is index fossils and sub-erathem stratigraphic units. A relative time scale is all the section's articles use. ↩
- 1a.
- 2.
Wise, Kurt P. “Towards a Creationist Understanding of 'Transitional Forms'.” CEN Technical Journal (now Journal of Creation) 9(2):216–222. 1995. A short essay in a creationist technical journal by a young-earth creationist paleontologist, whose author box gives an M.A. and a Ph.D. in palaeontology from Harvard. It defines stratigraphic, morphological and stratomorphic intermediates, grants that the fossil record confirms the higher-level series that evolution predicted, sketches a Flood model that might account for some of them, and names the whales as the series it cannot yet explain. This page uses it because it is the young-earth side's own most candid assessment of these sequences, and because its examples sort cleanly by rank. ↩
- 2a.
Page 219: “Creationists therefore need to accept this fact. It certainly CANNOT be said that traditional creation theory expected (predicted) any of these fossil finds.” CANNOT is capitalised in the original, as printed. Do not quote this sentence without its companion at p. 218, which gives the failed prediction it follows from. Wise's footnotes source every example on his list to mainstream literature and not to creationist works, including Hopson 1994 for the mammal-like reptiles, so a reader can check his claims without touching a creationist source. ↩ ↩
- 2b.
Page 218, section It Is a Very Good Evolutionary Argument: Under his own heading, the paragraph that ends in the concession opens with a failed prediction. Of Darwin's four stratomorphic-intermediate expectations, the commonness of inter-specific stratomorphic intermediates. “has been the most disappointing for classical Darwinists”. . The current lack of any certain example is what drove the development and acceptance of punctuated equilibrium. Stripping this is the most likely way our own side misuses the passage in the other direction, by making Wise concede more than he did. ↩
- 2c.
Page 219: Wise's list of confirmed stratomorphic intermediate species includes, verbatim, “Pikaia (between echinoderms and chordates)”. His reference 8 for it is. “Gould, S. J., 1989. Wonderful Life, Norton, New York, pp. 321–323.” Those pages place Pikaia inside the chordate phylum. The parenthesis is Wise's own gloss and is not supported by the pages cited. Echinoderms and chordates are both deuterostomes, so an animal between them would be a basal deuterostome lacking chordate characters, and the characters that caused Pikaia to be reclassified were the notochord and the myomeres, which are chordate characters. Verdict: misattributed. With this entry removed, Wise's concession has no surviving phylum-level example and its force lies at class level. ↩
- 2a.
- 3.
Uyeda, Josef C. et al. “The million-year wait for macroevolutionary bursts.” Proceedings of the National Academy of Sciences 108(38):15908–15913. 2011. A research paper that pools more than 8,000 body-size measurements of mammals, lizards and snakes, and birds, spanning 0.2 years to 357 million years and drawn from field studies, historical records, fossil series, and family trees of living species, then fits mathematical models with random chance built in. The trends article uses it to show where stasis (long spells with little change) ends: change does not accumulate up to about a million years, and divergence grows after that. ↩
- 3a.
Section Results and Discussion: After the models ruled out by Estes and Arnold, they write: “All of these models fail either because they require unrealistic values for microevolutionary processes or because bounded evolution is difficult to achieve under any set of parameter values. We conclude that some unspecified process of bounded evolution is responsible for the band we observe in our data (Fig. 1).” ↩ ↩
- 3a.
- 4.
Smith, William. Strata Identified by Organized Fossils, Containing Prints on Colored Paper of the Most Characteristic Specimens in Each Stratum. London: W. Arding. 1816. A book of engraved fossils, stratum by stratum, by the English mineral surveyor who drew the map of the strata of England and Wales. Its title page says the specimens were chosen to confirm the order of the British strata and to show how to identify each one, which is correlation by fossils with no dates in years. ↩
- 5.
Oppel, Albert. Die Juraformation Englands, Frankreichs und des südwestlichen Deutschlands, nach ihren einzelnen Gliedern eingetheilt und verglichen. Stuttgart: Ebner & Seubert. 1856. A monograph, issued from 1856 to 1858, that divides the Jurassic rocks of England, France and south-west Germany into thin zones, each named for a characteristic ammonite such as Ammonites planorbis, and matches the zones across the three countries. It is the classic case of correlating distant rocks by their fossils. ↩
- 6.
Lightner, Jean K. et al. “Determining the Ark Kinds.” Answers Research Journal 4:195–201. 2011. A paper in the journal of Answers in Genesis, setting out how its authors will work out which animals were the "kinds" on Noah's Ark. Where hybrid data is lacking, the authors use a method called the cognitum to find obvious groupings, and if a grouping looks too high in the classification they use the family level as the default. The sequence articles use it as the young-earth side's own statement that a created kind is usually the family, quoted from its own journal.
- 6a.
Page 198: The paper's own statement, which it attributes to earlier baraminology work. “From previous work in baraminology, researchers have suggested that the level of the baramin tends to fall at or near the taxonomic level of family (Wood 2006).” ↩
- 6a.
- 7.
Paleobiology Database. Paleobiology Database. n.d. A public database of published fossil finds, maintained by working paleontologists. Each occurrence records one taxon in one collection, with a literature reference and an age bracket rather than a single age. The child articles counted it in full in August 2026, at 2,001,053 occurrences in 277,490 collections, and each prints its own queries. It records what has been published, so it measures the literature as much as the rocks. ↩
- 7a.
Twenty-four boundary tests, each asking whether any occurrence's entire age bracket falls past the boundary. Below-first-appearance counts: mammals in Paleozoic rock 0; birds in Triassic or older rock 0; dinosaurs in Paleozoic rock 0; land vertebrates in Silurian or older rock 0; vertebrates and chordates in Precambrian rock 0 each; primates in Early Cretaceous or older rock 0; whales in Mesozoic rock 0; great apes in Eocene or older rock 0; grasses in Jurassic or older rock 0; trilobites in Precambrian rock 0; ammonoids in Ordovician or older rock 0; amniotes in Devonian or older rock 1; insects in Ordovician or older rock 1. The amniote hit is occurrence 2050687, identified in the database itself as "Dipnoa indet.", a lungfish, in Early Frasnian rock. The insect hit is occurrence 1661280, Aulocopsis simplex, from the Ordovician Volkhov Formation; Aulocopsis is a sponge genus name bound to an insect homonym. Above-last-appearance counts total 19, of which 3 are the Mesophyllum coral/alga homonym, 1 is a nomenclatural artifact, 1 shows the test boundary itself was wrong (dendroid graptolites are known into the Carboniferous), and 14 are the two best-known reworking cases in the literature: the Gulf Coast Danian ammonites of the Clayton and Kincaid formations, every one from a collection whose age bracket begins at the boundary itself, and Fort Union theropod material from the Hell Creek transition. The one genuinely open set is 25 pre-Jurassic angiosperm records, all leaf, seed or dispersed-pollen morphogenera whose affinity is disputed in the primary literature. A further 85 apparent Paleozoic "flowering plants" are form taxa and vanish entirely under the database's regular-preservation filter, so anyone quoting a raw count without that filter is quoting a filing convention. ↩
- 7a.
- 8.
Computed for the missing-transitions article against the full Paleobiology Database occurrence dump of 2,001,053 records, re-derived on 8 August 2026. Each occurrence carries an age bracket, not a point age, so only occurrences whose whole bracket falls inside a single international stage are used, and a loosely dated collection cannot invent or fill a gap. Genera found in three or more distinct stages are eligible. An internal gap is a stage between a genus's oldest and youngest occupied stage with no recorded occurrence of that genus. Result: 16,804 eligible genera, 75.9% with at least one internal gap, median gap 6.8 Myr. Two limits go with the figure: the bulk data carry no preservation flag, so trace and form taxa cannot be excluded and the extreme long-gap tail is contaminated, though the median is not; and the database records published occurrences, so it measures the literature rather than the rocks. ↩ ↩
- 9.
“Occurrence counts by geologic period for all life, from the Paleobiology Database.” Paleobiology Database. Aug 8, 2026. Counts of fossil occurrences for all life in each geologic block, from the database's diversity endpoint. Precambrian (Orosirian through Ediacaran) holds 3,259 occurrences and Paleozoic (Cambrian through Permian) 548,543. Everything below the Neogene holds 1,345,826, which is the Precambrian and Paleozoic totals plus Triassic 105,220, Jurassic 172,952, Cretaceous 248,292 and Paleogene 267,560. The order article uses these totals as its denominators: when it says a group is absent from Paleozoic rock, it means absent from 548,543 chances to appear. ↩ ↩
- 10.
“Occurrence counts for the genus Homo and the family Hominidae in the Paleobiology Database.” Paleobiology Database. Aug 8, 2026. The database's counts of fossil occurrences for the genus Homo: 238 in all, Pliocene 7, Pleistocene 191 and Holocene 40, with zero below the Pliocene. The family Hominidae has 619 occurrences, the oldest from the Miocene (170 in the Neogene and 449 in the Quaternary, in the period-level table). The order article sets these counts against the denominator of 1,345,826 occurrences below the Neogene, so the human count there is zero. ↩
- 11.
Thomas, Brian. “Pre-Flood Human Fossils Revisited.” Institute for Creation Research. Oct 30, 2015. A web article by an Institute for Creation Research science writer listing young-earth answers to the absence of human remains in Flood rock. It mentions three coal artifacts as possible pre-Flood objects and says they need testing for fraud, which makes it both a promoter of the coal finds and a caution against them. ↩
- 11a.
Opening sentence of the paragraph on coal artifacts: “Although we know of no undisputed human skeletal remains in Flood rocks, a few unique artifacts may have come from pre-Flood humans.” The artifacts Thomas then lists are the iron cup, the brass bell and the aluminium gear from coal, which he says need tests against fraud before a case is built on them. ↩
- 11a.
- 12.
Rana, Fazale. Dinosaur Blood and the Age of the Earth. RTB Press, Covina CA. 2016. A popular book by Fazale Rana, a biochemist with Reasons to Believe, an old-earth (day-age) Christian ministry. Its stated purpose is to explain why soft tissue can be preserved in fossils several hundred million years old. The soft-tissue article uses it for Rana's concession that the soft tissue is authentic, and for the decay figures and claims he reports. The ISBN is 978-1-886653-18-4. ↩
- 12a.
Page 30: “it does indeed appear that the soft tissue remnants isolated from a wide range of fossilized specimens are authentic endogenous materials, despite the protests of some skeptical paleontologists.” ↩
- 12a.
- 13.
Cavanaugh, D. P. et al. “Fossil Equidae: a monobaraminic, stratomorphic series.” Proceedings of the Fifth International Conference on Creationism, 143–153. Creation Science Fellowship, Pittsburgh. Edited by R. L. Ivey. 2003. A paper for the Fifth International Conference on Creationism, whose title calls the fossil horses a monobaraminic (one created kind), stratomorphic series. Its method, baraminic distance correlation with multidimensional scaling, is contested inside creationism. The horse article cites it for its title and for its authors' stated position, not for anything in its text. ↩
- 14.
Mángano, M. Gabriela, and Luis A. Buatois. “Decoupling of body-plan diversification and ecological structuring during the Ediacaran–Cambrian transition: evolutionary and geobiological feedbacks.” Proceedings of the Royal Society B 281:20140038. 2014. A research article that built a worldwide database of trace fossils (the tracks, burrows and trails that animals leave in sediment) from 369 rock units. Its authors found that body-plan diversification was complete by the Fortunian stage, while the restructuring of seafloor ecology came in Cambrian Stage 2. The Cambrian article uses it as the one line of evidence that needs no exceptional preservation. Mirror: PMC ↩
- 14a.
Table 1: Global ichnodiversity, the number of trace-fossil genera known worldwide, is 7 in the latest Ediacaran slice, which the authors call Nama (550–541 Ma), and 42 in the Fortunian. Global ichnodisparity, the number of architectural designs, is 5 and 22. The maximum depth of bioturbation is 1.0 cm in the Nama slice, 8 cm in the Fortunian and 100 cm in Cambrian Stage 2. ↩
- 14b.
Section Abstract: “Trace-fossil information strongly supports the Cambrian explosion, but allows for a short time of phylogenetic fuse during the terminal Ediacaran–Fortunian”. ↩
- 14a.
- 15.
Deline, Bradley et al. “Evolution of metazoan morphological disparity.” PNAS 115(38):E8909–E8918. 2018. A research article in PNAS that measures the range of animal body plans, which the authors call disparity, by placing living and fossil animals in a morphospace (a map on which animals sit according to their body features). The morphospace covers 212 taxa representing 34 phyla, the authors estimated the missing ancestral forms, and found that the living groups are clumped in it because intermediate forms went extinct. The Cambrian article uses it because it is the strongest published measurement against that article's argument, and because it reports that several groups kept expanding the range of body forms after the Cambrian. ↩
- 15a.
Section Abstract: The clumpiness of morphospace occupation by living clades. “is a consequence of the extinction of phylogenetic intermediates, indicating that the original distribution of morphologies was more homogeneous.” The design is what gives the claim its force: they placed fossils and reconstructed phylogenetic ancestors into a kingdom-wide morphospace, so the intermediates are estimated rather than assumed absent. ↩
- 15a.
- 16.
Gould, Stephen Jay. Wonderful Life: The Burgess Shale and the Nature of History. Norton, New York. 1989. A bestselling book by the paleontologist Stephen Jay Gould about the Burgess Shale, a Cambrian fossil deposit that preserves soft-bodied animals, and about what its strange animals mean for the history of life. Gould argues that the Burgess animals had a wider range of body designs at the start of animal life, and that later history was one of elimination rather than expansion. The Cambrian article uses it for Gould's own statements about the Burgess fauna, his test against the Solnhofen limestone, his measurement of 708 spindle diagrams, and the epilogue on Pikaia that Wise cites. ↩
- 16a.
Pages 321–323, section An Epilogue on Pikaia: “Pikaia is not an annelid worm. It is a chordate, a member of our own phylum—in fact, the first recorded member of our immediate ancestry.” These are the exact pages Kurt Wise cites for the claim that Pikaia lies between echinoderms and chordates. ↩
- 16a.
- 17.
Stanley, Steven M. “Estimates of the magnitudes of major marine mass extinctions in earth history.” Proceedings of the National Academy of Sciences 113(42):E6325–E6334. 2016. A re-estimate of the size of the major marine extinctions by a University of Hawaii palaeontologist. It corrects for background extinction and for the backward smearing of last appearances, and finds most events smaller than usually quoted, the end-Permian at about 81 % of species. Mirror: PMC ↩
- 17a.
Section Abstract: “They indicate that only ∼81% of marine species died out in the great terminal Permian crisis, whereas levels of 90–96% have frequently been quoted in the literature. Calculations of the latter numbers were incorrectly based on combined data for the Middle and Late Permian mass extinctions. About 90 orders and more than 220 families of marine animals survived the terminal Permian crisis … Life did not nearly disappear at the end of the Permian, as has often been claimed.” ↩
- 17a.
- 18.
Jeanson, Nathaniel T., and Jason Lisle. “On the origin of eukaryotic species' genotypic and phenotypic diversity.” Answers Research Journal 9:81–122. 2016. A young-earth model of how species diversified within created kinds after Creation and after the Flood, by two young-earth creationist scientists. ↩
- 18a.
Section General Aspects of the Young-Earth Creation Speciation Model: “These layers contain a tremendous amount of species' diversity, implying that a massive burst of speciation took place in just a few hundred years”. “Explaining all of this diversity in just a few hundred years is the most challenging explanatory task that the YEC species' origins model faces.” ↩
- 18a.
- 19.
Tomkins, Jeffrey P., and Timothy L. Clarey. “Developing a Comprehensive Model of Global Flood Paleontology: Integrating the Biostratigraphic Record with Global Megasequence Deposition.” Proceedings of the Ninth International Conference on Creationism 9:561–587. Cedarville University. 2023. The Institute for Creation Research's own account of how its megasequence Flood model explains the fossil record, written by its geneticist and its director of research. It maps Paleobiology Database occurrences onto Clarey's six megasequences and states ICR's position on every major extinction: none is a real extinction, each is a level where one ecological zone stopped being buried. It concedes that the marine end-Permian losses are "more difficult to explain." ↩
- 19a.
Page 563: “Creation scientists do not consider these as true “extinction” events. Instead, these horizons are interpreted as major shifts in the burial pattern of fossils during the Flood. So-called extinctions are merely the level at which certain fossils were no longer being actively buried, so they disappear upward in the geological column.” ↩
- 19b.
Page 577: “Our interpretation still has a bit of difficulty explaining the trackways and footprints found in some layers of the Cenozoic. It is possible some of these layers have been misidentified and should be Pleistocene (post-Flood), but more research is needed on each site.” ↩
- 19a.
- 20.
Kelley, Brian M. et al. “Prolonged and gradual recovery of metazoan-algal reefs following the end-Permian mass extinction.” Geology 51(11):1011–1016. 2023. Field mapping, satellite imagery and 164 thin sections through the oldest and thickest Lower to Middle Triassic platform-margin reef known, at the Great Bank of Guizhou in southern China. It records the order in which the reef builders appear. ↩
- 20a.
Page 1012: “The reef initiated in the upper Spathian (Payne et al., 2006) and persisted in situ to upper Pelsonian or lower Illyrian strata (Kelley et al., 2020), reaching a stratigraphic thickness of ∼900 m (Lehrmann et al., 1998). The reef facies is characterized by the occurrence of Tubiphytes boundstone.” Page 1014: “The lowest stratigraphic occurrence of identifiable reefbuilding metazoans (calcareous sponges) coincides with the base of zone 2, 365 m above the reef base … the first framework-contributing calcareous algae (Fig. 4L; 665 m above the reef base), and the first scleractinian corals (Figs. 4M and 4N; 895 m above the reef base).” ↩
- 20a.
- 21.
Arithmetic from Mass Extinctions. 900 m of reef in at most the 50 days ICR assigns to the whole Absaroka (Days 40 to about 90) is 18 m a day, or 6,570 m a year. Divided by 25 mm a year, the top of the range Montaggioni gives for average vertical accretion of modern sheltered reef margins, the ratio is about 263,000. The Guizhou reef spans only part of the Absaroka, so the true requirement on ICR's timetable is higher. ↩
- 22.
Oard, Michael J. “Argentina egg site supports BEDS model.” Journal of Creation 30(1):6–8. 2016. A short paper reading a study of an Argentine nesting site as support for BEDS. It gives the model's window for dinosaur activity, Day 40 to about Day 120. Mirror: Creation.com ↩
- 22a.
Page 8: “In the Creation model the dinosaur eggs and tracks were most likely made between Day 40 and about Day 120 of the Flood.” ↩
- 22a.
- 23.
Erickson, Gregory M. et al. “Dinosaur incubation periods directly determined from growth-line counts in embryonic teeth show reptilian-grade development.” Proceedings of the National Academy of Sciences 114(3):540–545. 2017. Counts daily incremental lines of von Ebner in the teeth of near-hatching embryos of Protoceratops andrewsi and Hypacrosaurus stebingeri and adds a conservative pre-tooth interval to give minimum incubation periods. The first direct measurement of dinosaur incubation time. Mirror: PMC ↩
- 23a.
Section Results: “However, the time elapsed in forming the oldest functional tooth was determined by summing the age of the younger functional tooth (55.27 d) and the tooth family replacement rate (44.18 d) (Materials and Methods and Fig. S1). This finding equates to a value of 99.45 d. Again, because the hatchling teeth conservatively began formation at 42% of incubation time (72.02 d), this reveals a minimum incubation period of 171.47 d.” ↩
- 23a.
- 24.
Garner, Paul. “Where is the Flood/post-Flood Boundary? Implications of Dinosaur Nests in the Mesozoic.” CEN Technical Journal 10(1):101–106. 1996. A young-earth geologist of the Biblical Creation Society surveys the in situ nest literature to 1995 and concludes the Mesozoic must be post-Flood. The one creationist paper that states the nest problem in full; its stratigraphic facts are taken from the excavators' own reports. ↩
- 24a.
Page 105: “Even more damaging to Oard's thesis are the localities where nests occur on several successive horizons. … How are we to accommodate several successive nest-building periods within 150 days, remembering that we also have to leave sufficient time for the rest of the Mesozoic, the entire Palaeozoic, and possibly a considerable portion of the Proterozoic to be deposited before the dinosaurs can even begin to build the first nest? Examples such as these stretch Oard's Flood chronology beyond breaking point.” ↩
- 24b.
Page 105: “The Flood/post-Flood boundary should therefore be sought in the pre-Triassic record.” ↩
- 24a.
- 25.
Morris, John D. “The Paluxy River Mystery.” ICR Impact (151). Jan 1, 1986. Published in Acts & Facts 15(1). The Institute for Creation Research's withdrawal of the claim, written by the author of the 1980 book that had promoted it; Morris was later ICR's president. Paragraph numbers count from the first body paragraph. ↩
- 25a.
Paragraph 19: “Even though it would now be improper for creationists to continue to use the Paluxy data as evidence against evolution, in the light of these questions, there is still much that is not known about the tracks and continued research is in order. We stand committed to truth, and will gladly modify or abandon our previous interpretation of the Paluxy data as the facts dictate.” The final paragraph. The first clause is often quoted alone, which overstates the withdrawal; "these questions" are the six points listed just above it, one of which is the "chemical agents" line. ↩
- 25a.
- 26.
Johns, Warren H. “Puzzle of the missing angiosperms in the fossil record.” Journal of Creation 36(2):106–111. 2022. A review in Creation Ministries International's journal, by a creationist, of three creationist claims of flowering-plant pollen in Precambrian and Cambrian rock: the Grand Canyon, the Salt Range of Pakistan and the Roraima Formation. It concludes that all three are contamination and asks creationists to stop using them. Its abstract places the Roraima in Suriname; the body correctly says British Guiana. ↩
- 26a.
Page 109: “The conclusion is that all three of the major sites of purported Precambrian and Cambrian pollen can be now explained as contamination. The questionable evidence for Precambrian and Cambrian angiosperm pollen of Grand Canyon, the Punjab of Pakistan, and the Roraima Formation of South American should be added to the list of arguments that creationists should not use to support creation.” ↩
- 26a.
- 27.
Garner, Paul et al. “Flood models.” TJ 14(3):79–80. 2000. A letter in which the four British creationists who in 1996 had put the end of the Flood in the Paleozoic, making the end-Permian and everything above it post-Flood, say they no longer hold that model. ↩
- 27a.
Closing paragraph: “None of us is satisfied with the model that we proposed in 1996. In the light of the problems encountered, our thinking has moved on, albeit not in a direction that McIntosh et al. would approve of.” The four signatories are Paul Garner, Michael Garton, Steven Robinson and David Tyler. Garner's 1996 nest paper had argued for the same low placement of the Flood's end. ↩ ↩
- 27a.
- 28.
Reeves, Colin R. “A Critical Evaluation of Statistical Baraminology: Part 1—Statistical Principles.” Answers Research Journal 14:261–269. Jul 14, 2021. A critique of the statistics behind baraminic distance correlation and its multidimensional-scaling companion, with a second part proposing ordinary cluster analysis in their place. Reeves is a statistician at the Applied Mathematics Research Centre, Coventry University, and writes as a creationist. ↩
- 28a.
Page 261, section abstract: “This paper will argue that these methods are based on a shaky understanding of statistical principles, and that their use ought to be abandoned.” ↩
- 28a.