Paranthropus

The robust australopiths were small-brained, small-bodied bipeds with the biggest cheek teeth of any hominin. Tooth chemistry shows East African boisei ate mostly grasses or sedges, not nuts. Every young-earth writer calls them non-human, but their enamel proteins sit nearer humans than apes, and their dates need post-Flood accelerated decay.

By AI (Claude Opus 5.5, thinking level unavailable) Draft:  October 2026

"The apparent discrepancy between microwear and functional anatomy is consistent with the idea that P. boisei presents a hominin example of Liem’s Paradox, wherein a highly derived morphology need not reflect a specialized diet." — Peter Ungar, Frederick Grine and Mark Teaford, PLoS ONE, 20081

"Furthermore, repeated studies of Paranthropus, a “robust” australopithecine, support recognizing them as their own nonhuman created kind." — Marcus Ross, Peter Brummel and Todd Wood, Proceedings of the Ninth International Conference on Creationism, 20232

Summary

Paranthropus is the genus name for the "robust" australopiths:  small-brained, upright-walking hominins with enormous jaws and cheek teeth.  Three species are widely accepted.  P. robustus comes from South African caves, named by Robert Broom in 1938.3  P. boisei comes from East Africa, named from Mary Leakey's 1959 skull from Olduvai Gorge.4  P. aethiopicus is the older East African form, best known from the "Black Skull" found in 1985.56  A fourth, P. capensis, was proposed in 2025 for a single jaw that had sat in Homo for decades.7  On the standard time scale they lived from about 3.0 to about 1.0 million years ago.8910

The numbers.  Brains averaged about 410 to 530 cubic centimetres, against a chimpanzee average of 369.811  Bodies averaged about 32 to 49 kilograms, depending on species and sex, if their legs were proportioned like ours.12  The East African upper second molar averages 220 square millimetres of crown, against 158 in Lucy's species and 164 in early Homo.9  Large males carried a sagittal crest, a bony ridge along the top of the skull that anchored huge chewing muscles.8

The "Nutcracker Man" picture is wrong for P. boisei.  Its teeth and jaws look built for cracking hard nuts and seeds.  The chemistry of its enamel says it ate mostly grasses or sedges:  about 77 percent of its carbon came from those plants, in 24 teeth from 22 individuals.13  The scratches on its molars show no especially hard or tough food in the days before death.1  The South African P. robustus ate a more varied diet that sometimes included hard items.1415  The lesson cuts both ways in the origins debate:  anatomy shows what an animal could eat, not what it did eat.1

Most analyses find that the robust species form one real group, but critics argue that the chewing traits behind it can evolve more than once.  Strait, Grine and Moniz found the group in all eight of their analyses, including one that left the chewing traits out.16  The Black Skull's own describers argued that the robust features arose "in parallel".5  Bernard Wood and Paul Constantino set out both cases in 2007 and kept the genus name for what they called a "strong possibility" of one group.88

Enamel proteins from four P. robustus teeth, published in 2025, are the only molecular evidence.  They identified two males and two females and found one variable site.  On 16 informative amino-acid positions, all four sequences "appear closer to those in the Homo clade than to any other primate," though the authors say a firm tree needs more coverage.17  No ancient DNA has been recovered from any African hominin older than about 20,000 years.17

Young-earth writers agree that the robust australopiths were not human.  Marvin Lubenow called the australopiths "simply extinct primates."6  Peter Line called them "mere extinct apes."18  Todd Wood's statistical baraminology makes Paranthropus a created kind of its own,19 and Ross, Brummel and Wood repeat that in 2023.2  They disagree about which kind.  Line suggests the Black Skull may belong with gorillas;18 Sigrid Hartwig-Scherer put all australopiths, robust ones included, into one created "basic type".20  Their evidence is mainly the skull and teeth, with brain size, the inner ear and a few limb bones.  None of them has yet answered the 2025 hand, which shows a human-like thumb and a walking foot,21 or the proteins.

Tools reopen an old question.  Louis Leakey first announced the Olduvai skull as "the oldest yet discovered maker of stone tools."4  That claim passed to Homo habilis in 1964.22  At Nyayanga in Kenya, a Paranthropus molar was found in place with Oldowan tools and a butchered hippopotamus, and no Homo.9  Ross, Brummel and Wood accept that simple Oldowan flakes might be the work of non-humans.2

The dates are the hard part for a young-earth reading.  The fossils are dated by potassium-argon and argon-argon on volcanic ash in East Africa, and by uranium-lead on flowstone, palaeomagnetism and other methods in South Africa.232425  Ross, Brummel and Wood place "all hominin remains" after Noah's Flood.2  Fitting 1.4 to 3.0 million years of measured decay into the roughly 4,500 years since the Flood requires decay about 310 to 670 times faster than today, after the Flood.26  The site's South African australopiths article prices what that costs.

Verdict.  The robust australopiths were not human, and on that the evidence and both sides agree.  Calling them simply "apes" undersells them:  they walked upright, had human-like thumb proportions, and their few protein sequences group with humans.  Wood's separate created kind fits this better than placing them with gorillas.  The diet results are a caution against reading behaviour from bones, for every side.  The real cost for the young-earth account is the time scale, not the anatomy.

Part 1: The finds

Kromdraai, 1938: the first robust skull

The first robust australopith came out of a South African hillside in a schoolboy's pocket.  In June 1938 Gert Terblanche found "much of the skull and lower jaw of a new type of anthropoid" in bone breccia near Kromdraai, a couple of miles from the Sterkfontein caves.3  Robert Broom tracked him to his school and "found the boy with four of what are perhaps the most valuable teeth in the world in his trouser pocket."3  Broom named it Paranthropus robustus.3  Paranthropus is Greek for "beside man".

Broom estimated its brain at "about 600 c.c."3  Later measurements of the species came out lower, as Part 2 shows.  He saw these South African animals as "large-brained anthropoids which resemble man in the shape of their premolars and in having relatively small canines."3  His word for the animal itself was "ape":  "The skull is that of a large ape, larger than most male chimpanzees".3  He guessed its age as Middle Pleistocene, adding that "more work will have to be done" before any of the skulls could be dated.3

The nearby cave of Swartkrans later produced "the largest collection of specimens attributed to P. robustus."17  The cave at Drimolen gave the most complete skulls, DNH 7 and the male DNH 155.27

Olduvai, 1959: "Zinjanthropus" and the toolmaker claim

Mary Leakey found the skull known as OH 5 at Olduvai Gorge in Tanzania in 1959.21  Louis Leakey named it Zinjanthropus boisei.  It lay on what he called "a well-defined living floor of the Oldowan, pre-Chelles-Acheul, culture," with stone tools and broken animal bones.4  He drew the conclusion that made it famous:  "It therefore seems that we have, in this skull, an actual representative of the type of ‘man’ who made the Oldowan pre-Chelles-Acheul culture."4  He ended by calling it "the oldest yet discovered maker of stone tools."4

Leakey did not put OH 5 in the human genus.  He called it "patently a member of the sub-family Australopithecinae" and said it recalled Paranthropus in its sagittal crest and its small front teeth.4  He made a new genus because he judged that it "differs from both Australopithecus and Paranthropus much more than these two genera differ from each other."4  Few agreed.  Phillip Tobias's 1967 monograph on OH 5 "found no grounds for a generic distinction between Zinjanthropus and Australopithecus (i.e., Paranthropus)," and the name Zinjanthropus fell out of use.8  The quotation marks around ‘man’ are Leakey's own.

Young-earth writers tell this story often, and on the main point they are right.  Lubenow:  "Believing that they had found the first tool maker, Louis named the fossil Zinjanthropus, “East Africa Man.”"6  He also quotes Leakey's popular account in National Geographic in September 1960, which began with teeth "quite obviously human".6  Rupe and Sanford:  "At the time, the fossil was widely promoted to the public as the oldest human ancestor. It was thought that the stone tools found nearby were made by Zinj. This interpretation was retracted shortly thereafter with the discovery of Homo habilis".22  What these passages do not say is that Leakey's scientific paper placed the skull among the australopiths from the start, while listing several features it called like Homo, such as a palate "even more markedly like that of Homo than in Australopithecus".4  The scientific claim was "toolmaker", not "human".  Part 6 shows that the toolmaker question has now come back.

The Black Skull, 1985

KNM-WT 17000, the "Black Skull", came from 2.5-million-year-old sediments west of Lake Turkana in Kenya.  Alan Walker, Richard Leakey, John Harris and Frank Brown described it in 1986 as an early A. boisei.  Its brain was about 410 cubic centimetres, the only measured brain for the species now called P. aethiopicus.8  Its describers found these early skulls primitive in many features.  That led them to argue that robust and "hyper-robust" forms "developed many of their common features in parallel".5  The name aethiopicus itself came from a 1967 jaw from the Omo valley in Ethiopia.8

Fifty years of East African finds

Wood and Constantino's 2007 review lists the main P. boisei finds:  teeth from Olduvai in 1955;  OH 5 in 1959;  the Peninj jaw in 1964;  many skulls and jaws from the Omo and Koobi Fora from 1967 on, with the peak of discovery between 1966 and 1975;  a skull from Konso in Ethiopia in 1993;  and a jaw from Malema in Malawi, which "more than doubled the north–south range of P. boisei to over 2,000 km."88  The youngest, at Konso, are about 1.4 million years old on the standard scale.8

The finds since 2015

  • Drimolen, South Africa, 2020. Two papers described skulls about 2.04 to 1.95 million years old. DNH 152 is "the earliest definitive occurrence of Paranthropus robustus," and a child's skull from the same deposit, DNH 134, has "clear affinities to Homo erectus."25 DNH 155, an adult male, shares with DNH 7 "a suite of primitive and derived features unlike those seen in adult P. robustus specimens from other chronologically younger deposits." Its describers call this "the most highly resolved evidence yet of microevolutionary change within an early hominin species."27
  • Nyayanga, Kenya, 2023. Two Paranthropus molars came from deposits dated 3.032 to 2.581 million years, with 330 Oldowan artefacts.99 One of them, an upper molar, is "the largest hominin molar currently known."9
  • Koobi Fora, Kenya, 2025. KNM-ER 101000 gave the first hand and foot bones "unambiguously associated with craniodental material of P. boisei," from deposits "slightly older than 1.52 million years."2121 Until then, sixty-six years after the species was named, no hand bone could be tied to it with certainty.21
  • Swartkrans, South Africa, 2025. The SK 15 jaw, found in 1949 and long assigned to Homo erectus, was reassigned to Paranthropus and "tentatively" made the type of a smaller species, P. capensis.7 The same year, the first enamel proteins of P. robustus were published.17
Species Where Age on the standard scale (million years) Brain (cm³) Body mass, male / female (kg)
P. aethiopicus Kenya, Ethiopia about 2.7 to 2.3 410 (one skull) not known
P. boisei Ethiopia to Malawi about 2.3 to 1.4 mean 488 (10 skulls; 400–545) 49 / 34
P. robustus South Africa about 2.0 to 1.0 mean 533 40 / 32
Paranthropus sp. Nyayanga, Kenya 3.0 to 2.6 not known not known

The brain sizes are Wood and Constantino's;8 the body masses are McHenry's, on the assumption of human-like leg proportions.12  The age ranges are approximate;  Part 8 gives the dates and methods find by find.

Part 2: A chewing machine on two legs

The robust australopiths were defined by their heads.  Wood and Constantino sum up P. boisei as "the only hominin to combine a massive, wide, flat, face with a megadont postcanine dentition, molarized mandibular premolars, and a modest (mean ca. 450–500 cm³) endocranial volume."8  "Megadont postcanine" means very large teeth behind the canines.  "Robust" describes the jaws and teeth, not the body.

Teeth

P. boisei "has the biggest, flattest cheek teeth, and the thickest dental enamel of any known member of our tribe".1  The table gives average crown areas of the upper first and second molars, measured at the base of the crown.

Group Upper first molar (mm²) Upper second molar (mm²)
East African robust (boisei, aethiopicus) 189 (n = 5) 220 (n = 3)
P. robustus 160 (n = 14) 185 (n = 8)
A. afarensis (Lucy's species) 137 (n = 6) 158 (n = 7)
East African early Homo 142 (n = 8) 164 (n = 4)
Nyayanga molar KNM-NG 77315 278–282

The East African robust second molar is about 1.4 times the area of Lucy's and 1.3 times early Homo's.9  The front teeth went the other way.  Leakey listed "the great reduction in the size of the canines and the incisors" among the features OH 5 shared with Paranthropus.4

Brain and body

Brains were small.  The one measured P. aethiopicus braincase, the Black Skull, holds about 410 cubic centimetres.  Ten P. boisei skulls average 488, from 400 to 545.  The P. robustus mean is 533, and Wood and Constantino found it not significantly different from boisei (P = 0.36).8  For comparison, 240 adult chimpanzees average 369.11  Broom's first estimate of about 600 for the Kromdraai skull was too high.3

Bodies were small too.  Henry McHenry estimated average body masses from the sizes of leg joints.  On the assumption of human-like proportions:  P. robustus males 40 and females 32 kilograms;  P. boisei males 49 and females 34.  If ape-like proportions are assumed instead, the males come out 10 to 23 kilograms heavier.12  Wood and Constantino conclude that Paranthropus overlaps "both with other archaic hominins and with extant higher primates in both body mass and brain size."8

Crests and the sexes

The big males had sagittal crests, and the crests vary.  Wood and Constantino report "Substantial polymorphism in sagittal cresting patterns in the larger (presumed male) crania":  OH 5's crest is highest at the front, the Konso skull's at the back.8  A crest forms where the two temporal muscles, which close the jaw, meet on top of the skull.  Gorilla males have the same feature, which is why Peter Line compares the Black Skull to "a small male gorilla."18

How much of the variation is between sexes and how much is between populations is now being tested directly.  The Drimolen skull DNH 7 differs from the younger Swartkrans skulls in ways once put down to its sex, but the male DNH 155 shares those differences, so Martin and colleagues read them as change over time within one species.27  The enamel proteins of Part 5 identify the sex of four Swartkrans teeth directly.  One small-crowned tooth, SK 835, turned out to be male.  The authors conclude that "sexual dimorphism is an insufficient explanation for the observed variation within our Paranthropus sample set."17

Hands, legs and ears

From the neck down Paranthropus was an upright walker that also climbed.

  • Hand. The 2025 P. boisei hand had "essentially modern human-like intrinsic hand proportions. That is, the thumb was long relative to the palm and other fingers".21 The authors add that a long thumb is "a characteristic also exhibited by known species of Australopithecus," so it does not mark Homo.21 The same hand "converges on that of gorillas in ways that are consistent with manual food processing and would have facilitated powerful grasping, such as that used in climbing."21
  • Foot. The foot bones from the same individual show "a greater commitment to terrestriality than in earlier hominins."21
  • Leg. The first P. robustus shin bone, from Swartkrans, has internal bone structure inside the gorilla range at the ankle. Its describers conclude that P. robustus "exhibits features indicative of joint postures likely associated with frequent climbing", and also that this "does not imply that P. robustus was not bipedal."1010
  • Joint sizes. A 2021 study sorted the limb-joint proportions of P. robustus and P. boisei with the "more ape-like" group.28
  • Inner ear. The balance canals of South African crania "attributed to Australopithecus and Paranthropus resemble those of the extant great apes."29

The anatomy fits one description.  The robust australopiths were bipedal primates with ape-sized brains, ape-like balance organs and climbing limbs, a hand with human-like proportions, and the largest cheek teeth of any hominin.  Nothing in it suggests a human being, and no one on either side of the origins debate argues that it does.

Part 3: What they ate

The "Nutcracker Man" picture

For fifty years the teeth were read as tools for cracking nuts.  Ungar, Grine and Teaford put it plainly:  the "specialized morphology, which earned P. boisei the nickname ‘‘Nutcracker Man’’, suggests that this hominin could have consumed very mechanically challenging foods."1  Cerling and colleagues describe the same consensus:  the features "have been widely interpreted as adaptations to a diet that consisted of hard objects that required powerful peak masticatory loads."13  Lubenow repeats it:  "The ridiculously large molars indicated that the individual probably had lived on nuts and berries".6

Two methods measure diet directly, and both contradict the nutcracker picture for P. boisei.

Carbon in the enamel

Plants fix carbon in two main ways, and the difference stays in the teeth of whatever eats them.  Trees, shrubs and herbs use the C3 pathway.  Tropical grasses and sedges mostly use the C4 pathway,13 which leaves more of the heavy isotope carbon-13.  Tooth enamel records the ratio, written δ13C, and keeps it "even after millions of years".13

East African P. boisei ate mainly C4 plants.  Thure Cerling and colleagues measured 24 teeth from 22 individuals from Kenya and Tanzania.  "The average δ13C value for these samples was -1.3 ± 0.9‰", which corresponds to "a diet where C4 biomass comprises 77 ± 7%, with minimum and maximum values of 61 and 91%".13  The values did not change over the half million years the samples span.  The authors conclude that boisei "had a diet that was dominated by C4 biomass such as grasses or sedges," more C4 than any other hominin measured.13  The arithmetic is a straight-line mix between a pure C3 diet near −12 and a pure C4 diet near +2.30

The earliest Paranthropus already ate this way.  The Nyayanga teeth average −0.7 ± 0.4 ‰, "which demonstrates a heavy reliance on C4 foods."9

South African P. robustus was different.  Its carbon is consistent with "most of its dietary carbon (approximately 70%)" coming from C3 foods "favored by extant chimpanzees (Pan troglodytes) such as tree fruits".13  Laser sampling along single teeth found that its δ13C "often changed seasonally and interannually," so robustus "was not a dietary specialist."15

Scratches on the molars

Microwear records the last meals.  Food leaves microscopic pits and scratches on chewing surfaces, and they are replaced within days.  In living primates, complex, pitted surfaces go with hard foods and strongly aligned scratches with tough foods.1

The P. boisei molars show neither.  Ungar, Grine and Teaford examined seven individuals spanning "from as early as 2.27 Myr to as recently as about 1.4 Myr."1  "These all show relatively low complexity and anisotropy values. This suggests that none of the individuals consumed especially hard or tough foods in the days before they died."1

The P. robustus molars do show some hard food.  Compared with Australopithecus africanus, robustus "has more complex microwear textures, but is also more variable in complexity".  The authors conclude that "P. robustus consumed more hard and brittle items, but that both had variable and overlapping diets."14  One explanation is that robustus "‘‘fell back’’ on less preferred, mechanically challenging items at times of resource stress," as lowland gorillas do with tough foods.1

What it shows

Anatomy says what an animal could eat, not what it ate.  Ungar's team:  "craniodental functional morphology offers insights into what a hominin could have eaten, but not necessarily what it actually ate on a regular basis."1  For boisei, the giant flat molars may have been for grinding large amounts of tough, low-quality plants, "rather than hard objects."13  For robustus, they may have been for hard foods eaten only in lean seasons.  Either way, the same anatomy went with different diets in different species.

The methods have limits, and they should be stated.  Carbon cannot tell grass from sedge, and cannot tell a C4 plant from an animal that ate C4 plants;  Sponheimer's team lists "animals eating these foods" among the possibilities.15  Microwear covers only the last days of life, and the boisei sample is seven individuals.

The lesson applies to every side.  Evolutionary writers built a nutcracker story on bones and had to drop it when the chemistry came in.  Young-earth writers who read humanity or its absence from a hand shape, a brain size or a jaw are using the same kind of inference.  The robust australopiths are a reminder that it can fail.

Part 4: Is Paranthropus a real group?

The question is whether the robust species share a common ancestor that no other hominin shares, or whether big jaws and teeth evolved more than once.  If the first, Paranthropus is a natural group, a clade.  If the second, the robust look is convergence, and P. robustus might be closer to A. africanus while P. aethiopicus is closer to A. afarensis.  Both have been proposed:  Madupe and colleagues summarise that "Most researchers consider Paranthropus to be monophyletic," while similarities between those pairs "have raised the possibility of paraphyly or even admixture between species."17

The case for one group

  • Strait, Grine and Moniz, 1997. Sixty skull and tooth characters, eight analyses done eight different ways. "All agreed that the "robust" australopithecines form a clade". One of the eight left out the chewing characters entirely. "Trees in which "robust" australopithecines are paraphyletic were found to be extremely unparsimonious."16
  • Earlier studies. Wood reviewed fifteen cladistic studies in 1988; all found the eastern and southern robust forms to be each other's closest relatives. He added that because several reused the same data, "this series of results is not as impressive as it appears."8
  • The genus name. Wood and Constantino keep Paranthropus "to recognize the strong possibility" that the robust species form one natural group.8

The case for convergence

  • The Black Skull. Its describers concluded that the robust forms "developed many of their common features in parallel".5
  • Chewing traits are prone to convergence. The average consistency index of hominin cladistic studies, about 0.65, "means that approximately 35% of the characters used in the analyses must have been independently acquired". Comparative evidence from other mammals suggests the chewing apparatus "might be the equivalent of a ‘‘homoplasy ghetto.’’"88
  • The order in time is awkward. The less specialised robustus is younger than the more specialised boisei. One group would need "several reversals in cranial morphology", or robustus existing long before it first appears. Separate origins would be "a striking case of homoplasy".8
  • The genus is getting more varied. A "gracile" Paranthropus, P. capensis, has been proposed,7 and the protein study found a variable site that might mark a distinct southern group.17

Robert Foley's 1990 review, as Lubenow quotes it, summed up the doubts:  "They are almost certainly not human. They are probably not robust, and they are possibly not even australopithecines. Worse still, it may be that they should not be treated as a group at all."6

The weight of the evidence favours one group, without settling it.  The decisive point is that the group survives when the chewing characters are removed.  But that analysis still used skulls and teeth, and no genetic data test it, since the only proteins come from one species.

What this means for the creationist sorting

Todd Wood's Paranthropus kind is built on the same skull-and-tooth character sets.  His 2010 analysis reworked Strait 1997, Strait and Grine 2004, Berger 2010 and others.19  So if the robust clade is a convergence artefact, the created kind built on those characters inherits the problem.  Wood saw part of it:  "the MDS results imply that there may be a separation between P. robustus/boisei and P. aethiopicus."19

Other young-earth models do not need the robust forms to be one group.  Sigrid Hartwig-Scherer's model expected parallel change within one created kind:  "during the radiation of the basic type, different species increased different trends to different degrees."20  Peter Line, by contrast, mocks the idea:  "I suppose this is why evolutionists like the word parallel so much, as in parallel evolution. Call it what you like, but is it science?"18  It is science when it can be tested, and Strait's analysis without chewing characters is that test.  Line's own suggestion, that the Black Skull might belong in the gorilla kind while other robust species stay elsewhere, would itself require the robust features to arise more than once.18

Part 5: The enamel proteins

What was found

In 2025 Palesa Madupe and colleagues published the first molecular evidence from Paranthropus.  No DNA survives;  as they note, "aDNA has never been successfully recovered from African hominin material older than ~ 0.02 Ma," that is, about 20,000 years.  Proteins in tooth enamel last longer, and informative protein sequences had already been recovered from older fossils in Eurasia.17  The team sampled four teeth from Swartkrans Member 1, dated 2.2 to 1.8 million years on the standard scale:  SK 830, SK 835, SK 850 and SK 14132.17

  • Coverage. Each tooth yielded peptides covering 540 to 780 amino-acid positions in eight to ten enamel proteins, and "A total of 425 amino acid positions were consistently identified in all four Paranthropus specimens".17
  • Sex. Peptides from AMELY, a gene on the Y chromosome, identified SK 835 and SK 850 as male. The other two were judged female by a threshold method that sexed eleven modern human teeth correctly.17
  • Placement. Against living and extinct great apes and humans, the team found 16 informative single amino-acid differences. "Based on these phylogenetically informative sites, all four Paranthropus protein sequences appear closer to those in the Homo clade than to any other primate". The authors add at once: "Given the limited total number of informative sites, conclusive phylogenetic results will require broader sequence coverage."17
  • Differences from us. "Out of the 16 identified single amino acid polymorphisms, only two, i.e. COL17A1-636 and ENAM-137, showed an allelic state different from that of present-day humans, Neanderthals, and Denisovans."17
  • Diversity. One site, position 137 of the protein enamelin, differs among the four teeth. The team suggests SK 835 "might be more distantly-related to the other three individuals" and may have belonged to a distinct group, while noting that the teeth "come from sediments accumulating within a 500 ka time window."1717

What proteins can and cannot show at these ages

They can show sex, a handful of variable sites, and a coarse position among the great apes.  That is all.  Four teeth, one species, about 425 shared positions and 16 informative sites cannot resolve fine relationships among hominins.  They cannot test whether Paranthropus is one group, because only P. robustus was sampled.  They cannot date anything.  The 2026 enamel proteome of Homo naledi did not settle that species' classification either;  the site's naledi article covers it.

The survival of the proteins is not, by itself, evidence of youth.  The same kind of method has recovered enamel protein fragments from Kenyan fossils dated 16 and 18 million years.31  In that study the number of fragments falls with the age of the site, "a clear decline of counts per fossil specimen over time for putative diagenetiforms," though not in the smaller set of high-confidence fragments.31  The Paranthropus peptides were short and heavily altered, with "advanced rates of diagenetically-induced amino acid modifications".17  A young-earth argument from protein survival would need a decay rate for enamel peptides and a burial temperature history showing that 2-million-year survival is impossible.  No one has published one.  The site's article on dinosaur soft tissue treats the general argument.

What it means for the young-earth placements

On the placement question, this is the one result in this article that clearly favours the mainstream over the "ape" reading.  If Paranthropus were simply a kind of ape in the sense of being closer to chimpanzees or gorillas than to humans, its enamel proteins should look more like theirs at the informative sites.  They do not.  On the sites available they sit with humans, which is what the evolutionary tree predicts for a species on the human side of the human–chimpanzee split.

The result does not show common descent, and it is thin.  Sixteen sites are few, and the authors themselves call a firm tree premature.  A young-earth biologist can reply that a separately created upright primate could share human-like enamel proteins by design, as it shares a human-like thumb.  That reply is available, but it predicts nothing:  it would have fitted a gorilla-like result just as well.  Wood's model, which makes Paranthropus its own created kind distinct from the chimpanzee and gorilla cluster, is not contradicted.  Line suggested the gorilla kind only for P. aethiopicus, which has no protein data;  the result tells against extending that idea to P. robustus.  No young-earth response to the proteins was found.

Part 6: Tools and hands

The toolmaker question has come back.  After 1964 the Olduvai tools were credited to Homo habilis, and the creationist retellings record that as Leakey's error.22  Lubenow went further:  "There is no way of ever proving that those tools were used by those australopithecines."6  Rupe and Sanford go further still and argue that true humans made the Olduvai tools:  "Why didn’t the Leakey’s consider the obvious possibility that the stone tools were manufactured and used by Homo sapiens or Erectus (as opposed to Habilis)?"  They point to human-looking foot, leg and finger bones from the same beds.22  Those bones belong to the debate over Homo habilis.  One finding here bears on it:  the 2025 P. boisei hand had human-like proportions,21 so a single human-looking hand bone cannot by itself show that a human was present.

Nyayanga reopened it.  At Nyayanga, on Kenya's Homa Peninsula, Thomas Plummer's team found 330 Oldowan artefacts and two hippopotamus butchery sites in deposits 3.03 to 2.58 million years old.99  One Paranthropus molar lay in place at a butchery site:  "a clear association of a hominin fossil with artifacts, raising the possibility that Paranthropus made and/or co-opted stone tools."9  The team kept the caveat:  "Although not found at Nyayanga, Homo was also present in eastern Africa at about the time of Nyayanga deposition (21), so the Nyayanga artifacts cannot be definitively attributed to a specific hominin genus."9

The 2025 hand makes tool use plausible but does not prove it.  Mongle and colleagues conclude that the fossils "suggest that P. boisei was capable of tool making and use in some capacity," while also supporting distinct diets for Paranthropus and Homo.21

Young-earth writers have an answer ready, and it is consistent.  Ross, Brummel and Wood note that simple Oldowan flakes "might plausibly have been produced by nonhuman apes," since a population of living monkeys produces similar flakes.  "Indeed, a recent report implicated Paranthropus in the use of Oldowan-type tools (Plummer et al. 2023)."2  If simple flaking is not a mark of humanity, a toolmaking Paranthropus poses no problem for a model in which it is not human.  The cost falls elsewhere:  the same writers cannot then use Oldowan tools as evidence that any early fossil was human, and Ross, Brummel and Wood say so:  "Even if we accepted the most ancient tools as human technology, we cannot confidently associate the artifacts with any specific fossil form that might otherwise be considered human."2

Part 7: Where young-earth writers place them

Every young-earth writer found puts the robust australopiths outside humanity.  They disagree about which created kind they belong to.  Ross, Brummel and Wood's 2023 table of young-earth opinion lists the robust australopithecines as "ape" in every column:  Lubenow, Hartwig-Scherer, Cuozzo, Rupe and Sanford, Bergman and colleagues, Sinclair and Wood, and their own study.  Cuozzo's entry carries a note that he calls the genus an ape but "does not discuss particular species."2  Here are the main positions in their authors' words.

Lubenow: extinct primates

Marvin Lubenow's Bones of Contention gives the australopiths little space on purpose:  "To give extensive coverage to the australopithecine fossil record is unnecessary. The australopithecines are simply extinct primates."6  His argument is that human fossils are as old as the australopiths, so they cannot be ancestors.  He describes P. boisei in the mainstream's terms, as having "massive jaws and teeth" and being "not considered to be in the direct human line."6

Line: "mere extinct apes", perhaps with gorillas

Peter Line's 2005 survey in the Journal of Creation says of the robust skulls:  "From the skulls of these creatures, it is obvious that there was nothing human-like about them."18  His conclusion covers every hominin outside Homo:  "The morphological features of the hominid fossils assigned to taxa outside the genus Homo indicate they were mere extinct apes."  He allows that several of them "may just represent variation within one or more ape kinds."18  For the Black Skull he goes further:  "it is possible that gorillas and aethiopicus belong to the same biblical kind."18

Rupe and Sanford: an extinct ape

Christopher Rupe and John Sanford's 2017 book Contested Bones calls OH 5 "an extinct ape far removed from the lineage of man," and says it "is now universally recognized by the paleoanthropological community to be a robust australopithecine."22

Hartwig-Scherer: one australopith kind

Sigrid Hartwig-Scherer, a German creationist biologist, defined created kinds as "basic types" by whether animals can hybridise:  "A given set of species belong to a basic type if they are connected directly or indirectly through hybridization."  For fossils she accepted that "the morphological data base is the only evidence available."20  In 1998 she put all australopiths into one basic type, Australopithecinae, separate from humans;  Wood notes that her scheme put the chimpanzees, bonobos and gorillas in another, "Gorillinae".19  The robust species were one branch of its diversification:  "Some have expanded the arboreal trend to the expense of the bipedal activities, others the brain size, or exceeded the special australopithecine traits such as dished faces and megadontia (A. robustus, A. boisei, A. arethiopicus)."20

Wood: a created kind of its own

Todd Wood's statistical baraminology is the only quantitative young-earth test, and it makes Paranthropus its own kind.  Wood set three predictions in advance, the second being "a discontinuity or at least a lack of continuity between the Homo monobaramin and species of the genera Australopithecus and Paranthropus (the so-called robust australopiths)."19  His analysis of eight published character sets put "the genus Paranthropus" in a group of its own, apart from both humans and the chimpanzee-gorilla cluster.19  "All four species of Homo in the dataset share significant, positive BDC, as do the three Paranthropus species."19  His conclusion was cautious:  "The robust australopiths (genus Paranthropus) can be provisionally classified as one holobaramin".19

Sinclair and Wood's 2021 rerun with different clustering methods found the same three groups, Paranthropus the third.32  On their larger 391-character data set they dropped Paranthropus before the analysis:  "We removed the Paranthropus taxa from the character set because they consistently formed a distant cluster, and there is no controversy over the conclusion that these taxa are not human."32  Ross, Brummel and Wood then wrote in 2023 that "repeated studies of Paranthropus ... support recognizing them as their own nonhuman created kind (Wood 2010, Brummel and Wood 2023)."2  The second citation is a slip:  Wood and Brummel's 2023 skeleton study used fourteen taxa and no Paranthropus.33  The support is Wood 2010 and Sinclair and Wood 2021, both on skulls and teeth.

O'Micks: brain and body size

Jean O'Micks clustered fourteen species on two numbers, average brain volume and body mass, and put P. boisei and P. aethiopicus in the non-human cluster with the other australopiths and H. habilis.34

Assessment

On "not human", the young-earth writers are right, and they agree with the mainstream.  No one in the sources read argues that Paranthropus was a human being or a human ancestor.  The anatomy in Part 2 supports them.

On "ape", the word needs care.  If "ape" means a non-human primate, it is correct.  If it means an animal that was more like a chimpanzee or gorilla than like a human in every way, it is not:  Paranthropus walked upright, had human-like thumb proportions, and its enamel proteins group with humans on the sites measured.2117  Line's gorilla-kind suggestion rests on a general likeness of the Black Skull to a small male gorilla's, and crests and big faces come with large jaws in many primates.  Wood's separate kind is the only young-earth placement tested with numbers, and it fits the anatomy and the proteins at least as well as any other.

The young-earth case rests mainly on skulls and teeth, and the new evidence is untouched.  No young-earth analysis of the Paranthropus hand, foot, leg bones or proteins was found.  Wood and Brummel's skeleton baraminology could add P. boisei now that its hand and foot are known.

Part 8: The dates

On the standard scale Paranthropus lived from about 3.0 to about 1.0 million years ago.  The East African dates come from volcanic ash, the South African dates from cave flowstone and other methods.

Find Age (million years) Main methods
Nyayanga molars, Kenya 3.032 to 2.581 apatite (U-Th)/He on two tuffaceous silts, magnetic polarity stratigraphy, correlation, fauna9
Black Skull, West Turkana about 2.5 dated sediments west of Lake Turkana5
Drimolen DNH 7, 152, 155 about 2.04 to 1.95 uranium-lead on flowstone, uranium-series ESR on teeth, palaeomagnetism25
Swartkrans Member 1 teeth 2.2 to 1.8 as cited by Madupe and colleagues17
OH 5, Olduvai Bed I 1.80 to 1.75 potassium-argon (1961), single-crystal argon-argon (1991)2324
KNM-ER 101000 hand, Koobi Fora a little over 1.52 position below the dated Koobi Fora Tuff complex21
Konso skulls, Ethiopia about 1.4 dated sediments8
P. robustus overall 2.22 to 0.96 South African cave dates10

The Olduvai date was the first of these to be measured, and it has held.  In 1961 Louis Leakey, J. F. Evernden and Garniss Curtis dated volcanic layers at the OH 5 site by potassium-argon.  They were candid that "the hominid-site dates fail to fall in the proper relative order but all are between 1·6 and 1·9 million years," and took the average, 1.75 million years.23  Thirty years later, argon-argon dating of single crystals put middle to upper Bed I at "1.80 Myr to 1.75 Myr."24  The site's articles on radiometric concordance and radiometric anomalies, which tells the KBS Tuff story from nearby Koobi Fora, show how such dates are cross-checked.  The South African cave dating is set out in The South African Australopiths.

Where young-earth writers put these layers.  Ross, Brummel and Wood give reasons to think the hominin fossils lie in local, post-Flood deposits with signs of occupation, and conclude:  "These general considerations strongly suggest that all hominin remains are post-Flood."2  Their Olduvai example builds a sequence of bedrock, lake, volcanic cones and stone tools, "without regard to the absolute dating of these features."2  Creation Ministries International puts the South African cave fills after the Flood as well.35

So the measured decay has to fit after the Flood.  On CMI's figure of about 4,500 years since the Flood, the East African dates of 1.4 to 3.0 million years need radioactive decay about 310 to 670 times faster than today, averaged over the whole post-Flood period.  The youngest South African robustus, at about 1 million years, needs about 210.  On Hardy and Carter's earliest possible Flood date, 3386 BC, the East African factors are about 260 to 550.2636  Young-earth physicists have placed accelerated decay in two episodes:  John Baumgardner, for example, puts "roughly 3.7 billion years' worth" in Creation Week and "up to about 600 million years' worth" in the Flood.37  Neither is after the Flood.  Michael Oard is the one young-earth writer found who accepts that it continued afterwards:  "This means that much accelerated radiometric decay has taken place after the Flood."38  No young-earth model has yet worked out how decay could run hundreds of times faster while people and animals lived through it.  The sibling article on the South African australopiths prices this in detail, including a cave count of cosmic-ray atoms that faster decay makes worse, and the site's heat problem article covers the energy.  Paranthropus adds no new physics to that problem, but it adds more sites and more methods:  potassium-argon, argon-argon and (U-Th)/He on volcanic material in Kenya, Ethiopia and Tanzania, and uranium-lead and ESR in South Africa, all of which would need the same post-Flood speed-up.

Objections and responses

1.  "Paranthropus is a missing link between apes and humans."  No current researcher says so.  The mainstream treats the robust australopiths as a side branch that died out;  Lubenow's summary of the mainstream view is accurate:  "it is not considered to be in the direct human line."6  Whatever Paranthropus shows about human origins, it does not show an ancestor.

2.  "If both sides agree Paranthropus was not human, it tells us nothing about origins."  It tells us something, but less than either side often claims.  On the evolutionary account it is one of several upright, small-brained hominins that lived beside early Homo;  at Drimolen, P. robustus and a child with "clear affinities to Homo erectus" come from the same deposit.25  On the young-earth account it is a separately created upright primate that went extinct.  The proteins, which group it with humans, are the piece that a young-earth model must explain and an evolutionary model predicts.  The anatomy alone does not decide between them.

3.  "The enamel proteins prove that Paranthropus shares an ancestor with us."  They do not prove it.  Sixteen informative sites are few, and the authors say "conclusive phylogenetic results will require broader sequence coverage."17  They are what common ancestry predicts, and a young-earth reply from common design fits any result equally well, which makes it weaker as an explanation, not false.

4.  "Proteins in two-million-year-old teeth show that the teeth are young."  Survival alone shows nothing about the date unless someone computes how long enamel peptides can last at that site's temperature.  The same methods find fragments in Kenyan teeth dated 18 million years, and the number of fragments falls with the dated age of the site.31  The Paranthropus peptides were short and heavily altered.17  No young-earth kinetic calculation was found.

5.  "Leakey's Zinjanthropus shows that paleoanthropologists push every skull as a human ancestor."  Leakey did overreach on the toolmaker claim, and young-earth writers are right to say so.6  But his own scientific paper kept OH 5 among the australopiths, even though his popular writing called its teeth "quite obviously human",46 and the name Zinjanthropus fell out of use after Phillip Tobias's 1967 study of the skull.8  The toolmaker question was then reopened in 2023 on new evidence, with an explicit caveat.9  That is the field correcting and reconsidering itself, which is what it should do.

6.  "The Olduvai dates were out of order, so the method is unreliable."  The 1961 potassium-argon dates were out of order within a narrow range, and the authors said so.23  Thirty years of improved methods moved the figure by less than three percent.24  For a young earth the issue is not a scatter of 0.3 million years in 1.75, but a factor of several hundred.

7.  "Parallel evolution is a fudge word."  Line asks of parallel evolution, "Call it what you like, but is it science?"18  It is a claim that can be tested.  Strait and colleagues tested it by removing the chewing traits, and the robust group survived.16  Young-earth models use the same idea:  Hartwig-Scherer expected species within one created kind to develop "different trends to different degrees."20

8.  "A crest like a gorilla's means Paranthropus was a gorilla kind."  A sagittal crest forms where very large jaw muscles meet on the skull, and it varies even among P. boisei males.8  The rest of the animal points elsewhere:  a foot committed to walking on the ground, a thumb in human proportion, and enamel proteins nearer humans than gorillas.212117  Line raised the gorilla possibility only for the Black Skull, and no protein data exist for that species.

9.  "The P. capensis jaw shows that experts cannot tell Homo from Paranthropus."  It shows that a single jaw can be misassigned for decades.  SK 15 was assigned to Homo erectus and is now classified with Paranthropus on the shape of its tooth row and the inner structure of its molars;  the new species name is offered "tentatively".7  That is a caution for everyone who builds on taxon labels, including baraminology, which takes the mainstream's species lists as its data.  It does not blur the difference between a whole Paranthropus skull and a whole Homo skull.

10.  "The nutcracker reversal shows that paleoanthropology is just storytelling."  The nutcracker idea was an inference from anatomy, and it was overturned by two independent measurements, microwear and carbon isotopes.113  That is a success for measurement over inference.  The young-earth argument should take the same lesson:  claims about what a fossil creature could do, made from its bones alone, are weaker than they look.

Issues and unanswered questions

  1. No young-earth analysis has used the new Paranthropus evidence. Wood's baraminology of the genus rests on skull and tooth characters from 1997 to 2010. The P. boisei hand and foot of 2025, the P. robustus leg bones of 2026 and the enamel proteins of 2025 have not been analysed by any young-earth writer found.
  2. Is Paranthropus one group? The cladistic answer is "probably", but the decisive characters are skull and teeth, and only one species has protein data. Proteins from P. boisei would test it directly.
  3. How many southern species were there? P. capensis rests on one jaw. The protein variant in SK 835 may mark a second group or ordinary variation, and Martin's Drimolen skulls point to change within one species. These three readings have not been reconciled.
  4. Did Paranthropus make tools? Nyayanga gives an association, not proof, and early Homo was in the region. A Paranthropus hand found with tools and no Homo would settle more.
  5. Body masses depend on an assumption. McHenry's figures assume human-like leg proportions; ape-like proportions add 10 to 23 kilograms to males.12
  6. Sources not read in full. Walker and colleagues' 1986 Black Skull paper, read only in its abstract; Robert Foley's 1990 review, known only as Lubenow quotes it; Deino's 2012 recalibration of Olduvai Bed I; Sponheimer and colleagues' 2023 review "Problems with Paranthropus"; and the 2026 Springer volume on Paranthropus palaeobiology. None of them is likely to change the verdicts, but the first two are quoted only at second hand here.
  7. The 1960 National Geographic article was not read. Leakey's "quite obviously human" is known here only as Lubenow quotes it.6 This article checked Leakey's scientific paper, not the popular press.
  8. Post-Flood accelerated decay has no worked-out model. Every Paranthropus date needs it, and no young-earth physicist has proposed how, when or why it ran after the Flood.

Verdict

The robust australopiths were not human.  Their brains were 410 to about 530 cubic centimetres, their bodies were small, their inner ears were ape-like, and they climbed as well as walked.  The mainstream and every young-earth writer found agree.

"Ape" is the right word only in the sense of "not human."  Paranthropus walked upright, had a thumb proportioned like ours, and its few protein sequences group with humans.  Of the young-earth placements, Todd Wood's separate created kind fits this best.  Placing the robust forms in the gorilla kind fits worst.  The protein result is the clearest point in this article for the evolutionary side, and it is thin.

"Nutcracker Man" ate grass or sedge.  Carbon isotopes and tooth wear overturned a fifty-year inference from anatomy.  The lesson, that bones show what an animal could do rather than what it did, applies to every side of the origins debate.

The dates are the young-earth account's real problem.  Ross, Brummel and Wood place all hominin fossils after the Flood.  That needs radioactive decay several hundred times faster than today after the Flood, across several methods, in the volcanic ash of three East African countries and the caves of South Africa.  No young-earth model supplies it.

Sources


  1. 1.

    Ungar, Peter S. et al.  “Dental Microwear and Diet of the Plio-Pleistocene Hominin Paranthropus boisei.”  PLoS ONE 3(4):e2044.  Apr 30, 2008.  The first quantitative microwear study of P. boisei, on the molars of the seven individuals whose wear surfaces survive, spanning most of the species' time range.

    1. 1a.

      Section Abstract:  “This specialized morphology, which earned P. boisei the nickname ‘‘Nutcracker Man’’, suggests that this hominin could have consumed very mechanically challenging foods.”  “These all show relatively low complexity and anisotropy values. This suggests that none of the individuals consumed especially hard or tough foods in the days before they died. The apparent discrepancy between microwear and functional anatomy is consistent with the idea that P. boisei presents a hominin example of Liem’s Paradox, wherein a highly derived morphology need not reflect a specialized diet.” ↩ ↩ ↩ ↩ ↩

    2. 1b.

      Section Introduction:  “Paranthropus boisei has the biggest, flattest cheek teeth, and the thickest dental enamel of any known member of our tribe, the Hominini [1,2].” ↩

    3. 1c.

      Section Introduction:  “That said, craniodental functional morphology offers insights into what a hominin could have eaten, but not necessarily what it actually ate on a regular basis.” ↩ ↩

    4. 1d.

      Section Introduction:  “The idea is that P. robustus ‘‘fell back’’ on less preferred, mechanically challenging items at times of resource stress when preferred foods were unavailable, much like modern-day lowland gorillas do with tough foods.” ↩

    5. 1e.

      Section Abstract:  “High microwear surface texture complexity and anisotropy in extant primates can be associated with the consumption of exceptionally hard and tough foods respectively.”  Section Introduction:  “Given that microwear forms and changes quickly (i.e., in the days before death) [12]”. ↩

    6. 1f.

      Section Materials and Methods:  “Nevertheless, these seven fossils span most of the known geochronological range of P. boisei, from as early as 2.27 Myr to as recently as about 1.4 Myr.” ↩

  2. 2.

    Ross, Marcus R. et al.  “Human History from Adam to Abraham:  Integrating Paleoanthropology with a Young-age Creation Perspective.”  Proceedings of the Ninth International Conference on Creationism, 66–87.  Cedarville University International Conference on Creationism.  Edited by J. H. Whitmore.  2023.  A young-earth synthesis by a paleontologist, a student and a biologist that sorts the hominin fossils into human and non-human, using baraminology and a survey of earlier creationist opinion, and places the human fossils in post-Flood history.  Its Table 2 compares six earlier young-earth treatments.

    1. 2a.

      Page 74:  “Furthermore, repeated studies of Paranthropus, a “robust” australopithecine, support recognizing them as their own nonhuman created kind (Wood 2010, Brummel and Wood 2023).” ↩ ↩ ↩

    2. 2b.

      Page 73, table 2:  The row "Australopithecus (other species, including “robust australopithecines”)" reads "ape" under Lubenow (1992, 2004), Hartwig-Scherer (1998), Cuozzo (1998), Rupe and Sanford (2017), Bergman, Line, Tomkins and Biddle (2020), Sinclair and Wood (2021) and the present study.  “Cuozzo considers the genus Australopithecus to be an ape (p. 101), but does not discuss particular species.” ↩

    3. 2c.

      Page 71:  “the simple flakes and cores of Oldowan tools might plausibly have been produced by nonhuman apes, given that similar artifacts have been produced by a population of extant monkeys (Proffitt et al. 2016). Indeed, a recent report implicated Paranthropus in the use of Oldowan-type tools (Plummer et al. 2023). Even if we accepted the most ancient tools as human technology, we cannot confidently associate the artifacts with any specific fossil form that might otherwise be considered human.” ↩ ↩ ↩

    4. 2d.

      Page 75:  “These general considerations strongly suggest that all hominin remains are post-Flood.” ↩ ↩

    5. 2e.

      Page 76:  “Again, without regard to the absolute dating of these features, we can see that a sequence of events occurred”. ↩

  3. 3.

    Broom, Robert.  “The Pleistocene Anthropoid Apes of South Africa.”  Nature 142:377–379.  Aug 27, 1938.  Broom's announcement of the Kromdraai skull and his naming of Paranthropus robustus, with a survey of the South African fossil apes then known.  Broom was the Transvaal Museum paleontologist who found most of the early South African australopiths.

    1. 3a.

      Page 377:  “In June of this year a most important new discovery was made. A schoolboy, Gert Terblanche, found in an outcrop of bone breccia near the top of a hill, a couple of miles from the Sterkfontein caves, much of the skull and lower jaw of a new type of anthropoid.” ↩

    2. 3b.

      Page 377:  “I naturally went to the school, and found the boy with four of what are perhaps the most valuable teeth in the world in his trouser pocket.” ↩

    3. 3c.

      Page 378:  “The skull is that of a large ape, larger than most male chimpanzees”. ↩

    4. 3d.

      Page 378:  “From the portion of the brain case preserved, I estimate the volume of the brain to have been about 600 c.c.” ↩ ↩

    5. 3e.

      Page 379:  “The skull may be referred to as the Kromdraai (pronounced ‘Kromdry’) skull, and may be given the name Paranthropus robustus.” ↩ ↩

    6. 3f.

      Page 379:  “Clearly, during the Pleistocene there lived in South Africa a number of large-brained anthropoids which resemble man in the shape of their premolars and in having relatively small canines, and in having the glenoid region, in at least some forms, remarkably human in structure.” ↩

    7. 3g.

      Page 379:  “It seems probable that the Sterkfontein skull is of Upper Pleistocene age, the Kromdraai skull of Middle Pleistocene and the Taungs skull probably of Lower Pleistocene ; though of course more work will have to be done before the geological ages of any of these skulls can be determined with more than probability.” ↩

  4. 4.

    Leakey, L. S. B.  “A New Fossil Skull from Olduvai.”  Nature 184:491–493.  Aug 15, 1959.  Louis Leakey's announcement of OH 5, found by Mary Leakey at site FLK I in Bed I of Olduvai Gorge, and his naming of Zinjanthropus boisei.  It gives the find's association with Oldowan tools, a list of the features by which he separated it from Australopithecus and Paranthropus, and his first measurements.

    1. 4a.

      Page 491:  “This skull was found to be associated with a well-defined living floor of the Oldowan, pre-Chelles-Acheul, culture.” ↩

    2. 4b.

      Page 491:  “It therefore seems that we have, in this skull, an actual representative of the type of ‘man’ who made the Oldowan pre-Chelles-Acheul culture.” ↩

    3. 4c.

      Page 491:  “The Olduvai skull is patently a member of the sub-family Australopithecinae, and in certain respects it recalls the genus Paranthropus. In particular, this is the case in respect of the presence of the sagittal crest, the great reduction in the size of the canines and the incisors”. ↩ ↩ ↩

    4. 4d.

      Page 491:  “the new skull from Olduvai, while clearly a member of the Australopithecinae, differs from both Australopithecus and Paranthropus much more than these two genera differ from each other.” ↩ ↩

    5. 4e.

      Page 493:  “the very deep palate which is even more markedly like that of Homo than in Australopithecus”.  Item (r) in Leakey's list of the features that set the new genus apart;  item (s) says the form of the cheek region "is that which is found in Homo". ↩

    6. 4f.

      Page 493:  “With the Taungs child, therefore, and the Australopithecus fossils from the lower beds at Sterkfontein, the new find represents one of the earliest Hominidae, with the Olduvai skull as the oldest yet discovered maker of stone tools.” ↩ ↩

  5. 5.

    Walker, Alan et al.  “2.5-Myr Australopithecus boisei from west of Lake Turkana, Kenya.”  Nature 322:517–522.  Aug 7, 1986.  The description of the Black Skull, KNM-WT 17000, and related jaws from West Turkana.  Its primitive features led the authors to argue that the robust features evolved more than once.

    1. 5a.

      Section Abstract:  “Specimens of Australopithecus boisei have been found in 2.5-Myr-old sediments west of Lake Turkana, Kenya. The primitive morphology of these early A. boisei suggests that robust and hyper-robust Australopithecus developed many of their common features in parallel and further that A. africanus is unlikely to have been ancestral to A. boisei.” ↩ ↩ ↩ ↩ ↩

  6. 6.

    Lubenow, Marvin L.  Bones of Contention:  A Creationist Assessment of Human Fossils.  Baker Books.  revised and updated edition.  2004.  The standard young-earth book on human fossils, first published in 1992.  Lubenow argues that true humans lived throughout the australopiths' time, so the australopiths cannot be human ancestors, and he uses the conventional dates to make that case.

    1. 6a.

      Page 38:  “Believing that they had found the first tool maker, Louis named the fossil Zinjanthropus, “East Africa Man.” The ridiculously large molars indicated that the individual probably had lived on nuts and berries, and so the fossil became affectionately known as “Nutcracker Man.”” ↩ ↩

    2. 6b.

      Page 39:  “discovery of “Zinj” in National Geographic, September 1960, Louis began his report, “The teeth were projecting from the rock face, smooth and shining, and quite obviously human (emphasis added).””  “What Louis claimed was “obviously human” turned out to be obviously nonhuman.” ↩ ↩ ↩

    3. 6c.

      Page 66:  “This comfortable arrangement was severely jolted by the discovery in 1985 of the famous “black skull,” KNM-WT 17000.” ↩

    4. 6d.

      Page 189:  “Paranthropus boisei, found in eastern Africa, has massive jaws and teeth and was probably a vegetarian. Dated at 2.0 million years ago to 1.4 million years ago, it is not considered to be in the direct human line.” ↩ ↩

    5. 6e.

      Page 247:  “Even my secular hero, Louis Leakey, made the mistake of thinking that the first Australopithecus boisei (Zinjanthropus) he found was a tool maker because the stone tools and the fossil were found together.”  “There is no way of ever proving that those tools were used by those australopithecines.” ↩ ↩

    6. 6f.

      Page 301:  “To give extensive coverage to the australopithecine fossil record is unnecessary. The australopithecines are simply extinct primates.” ↩ ↩

    7. 6g.

      Page 301:  “They are almost certainly not human. They are probably not robust, and they are possibly not even australopithecines. Worse still, it may be that they should not be treated as a group at all.”  Lubenow is quoting Robert Foley's review of Frederick Grine's 1988 volume Evolutionary History of the "Robust" Australopithecines, in the American Journal of Physical Anthropology 82 (1990), page 113.  Foley is a Cambridge paleoanthropologist. ↩

  7. 7.

    Zanolli, Clément et al.  “Taxonomic revision of the SK 15 mandible based on bone and tooth structural organization.”  Journal of Human Evolution 200:103634.  Mar 2025.  A micro-CT and shape study of the SK 15 jaw from Swartkrans, found in 1949 and long assigned to Homo, comparing its tooth arcade, chin region and internal tooth structure with Homo and Paranthropus.

    1. 7a.

      Section Abstract:  “SK 15 was originally attributed to Telanthropus capensis but is now generally attributed to Homo erectus/Homo ergaster, even if it was previously suggested to possibly belong to Australopithecus.”  “We thus tentatively attribute SK 15 to Paranthropus capensis, a more gracile species of Paranthropus than the other three currently recognized species of this genus”. ↩ ↩ ↩ ↩

  8. 8.

    Wood, Bernard, and Paul Constantino.  “Paranthropus boisei:  Fifty Years of Evidence and Analysis.”  Yearbook of Physical Anthropology 50:106–132.  2007.  The standard review of P. boisei:  the history of its discovery, its range in space and time, its anatomy with a table of distinctive features, its diet, and the evidence for and against Paranthropus as one natural group.  Bernard Wood is a leading specialist in early hominin systematics, not to be confused with the creationist Todd Wood.

    1. 8a.

      Page 106:  “Subsequently, a detailed and meticulous analysis of the OH 5 cranium (Tobias, 1967) also found no grounds for a generic distinction between Zinjanthropus and Australopithecus (i.e., Paranthropus).” ↩ ↩

    2. 8b.

      Page 107:  “These teeth were found at locality BK in Lower Bed II at Olduvai Gorge in Tanzania in 1955”.  Page 109:  “The rate of discovery of P. boisei reached its peak in the second decade (1966–1975) of the taxon’s history.” ↩

    3. 8c.

      Page 107:  “Another hominin mandible with postcanine megadontia, Omo 18.18, was recovered from the Omo Shungura Formation in southern Ethiopia in 1967 (Arambourg and Coppens, 1968). It was initially included in a separate genus and species, Paraustralopithecus aethiopicus, but this genus name has been abandoned”. ↩

    4. 8d.

      Page 107:  “the term Paranthropus should be used to recognize the strong possibility that megadont taxa in both regions form an adaptively distinctive monophyletic group.” ↩ ↩

    5. 8e.

      Page 109:  “The discovery of the Malema maxilla more than doubled the north–south range of P. boisei to over 2,000 km”. ↩

    6. 8f.

      Page 109:  “The geologically youngest known members of P. boisei are from Konso in Ethiopia (Suwa et al., 1997). These ca. 1.4 Ma fossils are slightly younger than specimens from Koobi Fora dated between 1.49 and 1.50 Ma.” ↩ ↩ ↩

    7. 8g.

      Page 111:  “P. boisei is the only hominin to combine a massive, wide, flat, face with a megadont postcanine dentition, molarized mandibular premolars, and a modest (mean ca. 450–500 cm³) endocranial volume.” ↩

    8. 8h.

      Page 118:  “But did the East and southern African ‘‘robust’’ taxa evolve from a recent common ancestor exclusive to themselves and thus form a monophyletic group, or did the various regional Paranthropus taxa evolve independently (Fig. 10)?”  “this would either imply several reversals in cranial morphology, or that P. robustus existed for several hundred thousand years prior to its current first appearance datum. Alternatively, if the two regional variants arose independently, then it would be a striking case of homoplasy with both lineages exhibiting a morphological trend towards masticatory hypertrophy and extreme postcanine megadontia.” ↩ ↩

    9. 8i.

      Page 119:  “Wood (1988) reviewed 15 hominin cladistic studies that had treated the East and southern African ‘‘robust’’ taxa as separate operational taxonomic units (OTUs). All of these studies concluded the two regional variants were sister taxa, but as some of the studies had used the same data sets, this series of results is not as impressive as it appears.” ↩

    10. 8j.

      Page 119:  “the ca. 0.65 average CI for hominin cladistic analyses means that approximately 35% of the characters used in the analyses must have been independently acquired (i.e., they are homoplasies).” ↩

    11. 8k.

      Page 119:  “There is also some comparative evidence from other groups of mammals (e.g., Maglio, 1975; Vrba, 1979, 1984) to suggest that the masticatory system might be the equivalent of a ‘‘homoplasy ghetto.’’ It should be noted, however, that Strait et al. (1997) excluded masticatory characters from one of their cladistic analyses and still found strong support for a Paranthropus clade.” ↩

    12. 8l.

      Page 124:  “since Paranthropus appears to overlap significantly both with other archaic hominins and with extant higher primates in both body mass and brain size, these variables provide no reason to suggest that P. boisei differed greatly from these other taxa in aspects of its life history.” ↩

    13. 8m.

      Page 125, table A1:  “The P. boisei mean value of 488 cm³/490 g (N = 10; range 400 (KMN-WT 17400)–545 (KGA-10-525) cm³”.  “The estimated endocranial volume and mass of P. boisei is most likely insignificantly larger than for P. aethiopicus for which there is only one data point (KNM-WT 17000 = 410 cm³/407 g). The P. boisei sample mean is also not significantly different (P = 0.36) from the P. robustus sample, even though the latter taxon includes individuals with larger brains resulting in a higher (533 cm³/535 g) mean brain volume and mass.”  "KMN" is the review's misprint for KNM. ↩ ↩ ↩ ↩

    14. 8n.

      Page 125, table A1:  “Substantial polymorphism in sagittal cresting patterns in the larger (presumed male) crania (Walker and Leakey, 1988; Brown et al., 1993; Wood et al., 1994). Some individuals have the greatest height of the crests anteriorly (e.g., OH 5) whereas some specimens have crests that are highest posteriorly (e.g., KGA-10-525).” ↩ ↩ ↩

  9. 9.

    Plummer, Thomas W. et al.  “Expanded geographic distribution and dietary strategies of the earliest Oldowan hominins and Paranthropus.”  Science 379(6632):561–566.  Feb 10, 2023.  The excavation report for Nyayanga on Kenya's Homa Peninsula:  Oldowan tools, butchered hippopotamus, isotope-measured Paranthropus teeth and the dating of the beds.  The supplementary materials give the tooth measurements and the comparison tables used here.  Mirror:  Hal.science

    1. 9a.

      Page 561:  “We describe sites at Nyayanga, Kenya, dated to 3.032 to 2.581 million years ago and expand this distribution by over 1300 kilometers.”  “The (U-Th)/He dating of apatite crystals yielded ages of 2.87 ± 0.79 Ma and 2.98 ± 0.50 Ma from two tuffaceous silts in NY-1”. ↩ ↩ ↩ ↩

    2. 9b.

      Page 563:  “We recovered 330 artifacts from the upper half of NY-1; 135 were recovered in situ from excavations 3 and 5”. ↩ ↩

    3. 9c.

      Page 565:  “which demonstrates a heavy reliance on C4 foods.”  The sentence gives the teeth's average δ13C as −0.7 ± 0.4 per mil. ↩

    4. 9d.

      Page 565:  “Paranthropus molar KNM-NG 77316 from the excavation 3 hippopotamid butchery site is a clear association of a hominin fossil with artifacts, raising the possibility that Paranthropus made and/or co-opted stone tools.” ↩ ↩

    5. 9e.

      Page 565:  “Although not found at Nyayanga, Homo was also present in eastern Africa at about the time of Nyayanga deposition (21), so the Nyayanga artifacts cannot be definitively attributed to a specific hominin genus.”  Reference 21 is the 2.8-million-year-old Ledi-Geraru jaw from Ethiopia. ↩ ↩

    6. 9f.

      Section Supplementary Materials, page 22:  “Left upper molar KNM-NG 77315 is the largest hominin molar currently known, measuring 18.1 mm buccolingually and >17.1 mm mesiodistally”. ↩

    7. 9g.

      Section Supplementary Materials, table S18, page 62:  Measured crown base areas of upper first and second molars, in square millimetres, with cusp areas from Wood and Engleman 1988.  First molar:  East African robust, P. boisei and P. aethiopicus, 189 (n = 5);  P. robustus 160 (n = 14);  A. afarensis 137 (n = 6);  East African Homo 142 (n = 8).  Second molar:  220 (n = 3), 185 (n = 8), 158 (n = 7) and 164 (n = 4).  KNM-NG 77315:  278 to 282.  The ratios in the text are 220 / 158 = 1.39 and 220 / 164 = 1.34. ↩ ↩

  10. 10.

    Cazenave, Marine et al.  “Swartkrans Paranthropus and Sterkfontein Australopithecus from southern Africa had different locomotor repertoires.”  Proceedings of the National Academy of Sciences 123:e2532193123.  2026.  A micro-CT study of the internal bone of the first P. robustus shin bone and its thigh bone, from Swartkrans, against Australopithecus from Sterkfontein, apes and humans.  Bone remodels to the loads it carries, so its internal structure records how the animal moved.

    1. 10a.

      Section Significance:  “We show clear functional differences: P. robustus exhibits features indicative of joint postures likely associated with frequent climbing, whereas Sterkfontein Australopithecus shows a pattern consistent with comparatively more frequent terrestrial bipedalism.”  Fig. 1 legend:  “The P. robustus specimen from Swartkrans Member 1 (SWT1/HR-2c) falls in the Gorilla convex hull”. ↩

    2. 10b.

      Section Discussion, paragraph 2:  “This evidence, however, does not imply that P. robustus was not bipedal. Its external lower limb morphology shows adaptations to bipedalism (SI Appendix, Fig. S1) and its internal bone structure also exhibits patterns compatible with extended limb bipedal locomotion as observed in modern humans.” ↩

    3. 10c.

      Section Introduction:  “the geologically younger P. robustus [2.22 ± 0.09 to 0.96 + 0.09 million years (Ma)]”. ↩ ↩

  11. 11.

    Gunz, Philipp et al.  “Australopithecus afarensis endocasts suggest ape-like brain organization and prolonged brain growth.”  Science Advances 6(14):eaaz4729.  2020.  A synchrotron CT study of A. afarensis braincases.  This article uses only its comparison figure for chimpanzee brain volume, from a sample of 240.

    1. 11a.

      Section Results:  “The average adult EV of A. afarensis (445 ml; SD, 60 ml) is larger than in Pan troglodytes (369 ml; SD, 37 ml; N = 240).” ↩ ↩

  12. 12.

    McHenry, Henry M.  “Body size and proportions in early hominids.”  American Journal of Physical Anthropology 87(4):407–431.  1992.  Body-mass estimates for early hominin species from 78 regression equations relating joint and bone sizes to known weights in modern apes and humans, applied to 95 fossils.  It is the source of the body masses most often quoted for the australopiths.

    1. 12a.

      Section Abstract:  “Using hindlimb joint size of specimens of relatively certain taxonomy and assuming these measures were more like those of modern humans than of apes, the male and female averages are as follows: Australopithecus afarensis, 45 and 29 kg; A. africanus, 41 and 30 kg; A. robustus, 40 and 32 kg; A. boisei, 49 and 34 kg; H. habilis, 52 and 32 kg.”  “If hominoid (i.e., ape and human combined) proportions are assumed, the males would be 10 to 23 kg larger and the females 4 to 10 kg larger.” ↩ ↩ ↩ ↩

  13. 13.

    Cerling, Thure E. et al.  “Diet of Paranthropus boisei in the early Pleistocene of East Africa.”  Proceedings of the National Academy of Sciences 108(23):9337–9341.  2011.  Carbon and oxygen isotope measurements on the enamel of 24 P. boisei teeth from Kenya, with earlier values from Tanzania, spanning about half a million years.  Cerling's laboratory at Utah developed much of the method of reading diet from fossil enamel.  The issue carried a commentary titled "The demise of Nutcracker Man".  Mirror:  PMC

    1. 13a.

      Section Abstract:  “The East African hominin Paranthropus boisei was characterized by a suite of craniodental features that have been widely interpreted as adaptations to a diet that consisted of hard objects that required powerful peak masticatory loads.”  “Here, we use stable isotopes to show that P. boisei had a diet that was dominated by C4 biomass such as grasses or sedges. Its diet included more C4 biomass than any other hominin studied to date, including its congener Paranthropus robustus from South Africa. These results, coupled with recent evidence from dental microwear, may indicate that the remarkable craniodental morphology of this taxon represents an adaptation for processing large quantities of low-quality vegetation rather than hard objects.” ↩ ↩ ↩ ↩

    2. 13b.

      Section Introduction:  “plants using the C3 photosynthetic pathway (most dicotyledonous plants including trees, shrubs, forbs, herbs) and those using the C4 pathway (predominantly tropical grasses and sedges, which are monocotyledonous plants)”. ↩

    3. 13c.

      Section Introduction:  “dietary carbon remains locked in tooth enamel even after millions of years”. ↩

    4. 13d.

      Section Introduction:  “Carbon isotope studies of P. robustus from South Africa indicated that it consumed some plants using C4 photosynthesis such as tropical grasses or sedges, but were also consistent with most of its dietary carbon (approximately 70%) having been derived from the C3 food items favored by extant chimpanzees (Pan troglodytes) such as tree fruits”. ↩

    5. 13e.

      Section Results:  “The δ13C values of P. boisei do not change over the half million years for which samples were available (r2 = 0.10). The average δ13C value for these samples was -1.3 ± 0.9‰ (24 teeth from 22 individuals), with a maximum value of +0.7‰ and a minimum value of -3.4‰ (Table 1). Using estimates of +2 and -12‰ for a “pure-C4 grazing” or “pure-C3 browsing” diet (14), the δ13C values for P. boisei correspond to a diet where C4 biomass comprises 77 ± 7%, with minimum and maximum values of 61 and 91%, respectively.” ↩ ↩ ↩

  14. 14.

    Scott, Robert S. et al.  “Dental microwear texture analysis shows within-species diet variability in fossil hominins.”  Nature 436:693–695.  Aug 4, 2005.  The first application of three-dimensional microwear texture analysis to fossil hominins, comparing P. robustus with A. africanus after calibrating the method on living primates of known diet.

    1. 14a.

      Section Abstract:  “This latter species has more complex microwear textures, but is also more variable in complexity than A. africanus. This suggests that A. africanus ate more tough foods and P. robustus consumed more hard and brittle items, but that both had variable and overlapping diets.” ↩ ↩

  15. 15.

    Sponheimer, Matt et al.  “Isotopic evidence for dietary variability in the early hominin Paranthropus robustus.”  Science 314(5801):980–982.  Nov 10, 2006.  Laser-ablation carbon isotope profiles along single P. robustus teeth from Swartkrans, which record diet season by season over the time each tooth grew.

    1. 15a.

      Section Abstract:  “However, laser ablation stable isotope analysis reveals that the delta13C values of Paranthropus robustus individuals often changed seasonally and interannually. These data suggest that Paranthropus was not a dietary specialist and that by about 1.8 million years ago, savanna-based foods such as grasses or sedges or animals eating these foods made up an important but highly variable part of its diet.” ↩ ↩ ↩

  16. 16.

    Strait, David S. et al.  “A reappraisal of early hominid phylogeny.”  Journal of Human Evolution 32(1):17–82.  1997.  A cladistic analysis of sixty skull and tooth characters across nine hominin species, run eight ways to test how robust its results were to coding choices.  Wood's 2010 baraminology reanalysed this data set.

    1. 16a.

      Section Abstract:  “All agreed that the "robust" australopithecines form a clade, A. afarensis is the sister taxon of all other hominids, and the genus Australopithecus, as conventionally defined, is paraphyletic.”  “(6) masticatory characters were excluded”.  “Trees in which "robust" australopithecines are paraphyletic were found to be extremely unparsimonious.” ↩ ↩ ↩

  17. 17.

    Madupe, Palesa P. et al.  “Enamel proteins reveal biological sex and genetic variability in southern African Paranthropus.”  Science 388(6750):969–973.  May 29, 2025.  Mass-spectrometry sequencing of protein fragments from the enamel of four P. robustus teeth from Swartkrans, about two million years old on the standard scale.  The Copenhagen group that led it had earlier published enamel proteomes from Homo antecessor and from early Pleistocene animals at Dmanisi in Georgia.  It is the first molecular evidence from any Paranthropus.  Mirror:  Eprints.whiterose.ac.uk

    1. 17a.

      Section Abstract:  “Paranthropus robustus is a morphologically well-documented Early Pleistocene hominin species from southern Africa with no genetic evidence reported so far.”  “A single amino acid polymorphism and the enamel-dentine junction shape variation indicate potential subgroups present within southern African Paranthropus.” ↩ ↩

    2. 17b.

      Section Introduction:  “Most researchers consider Paranthropus to be monophyletic (3) however, morphological similarities between P. robustus and A. africanus (4, 5), and between P. aethiopicus and A. afarensis (6, 7), have raised the possibility of paraphyly or even admixture between species (8, 9).” ↩

    3. 17c.

      Section Introduction:  “aDNA has never been successfully recovered from African hominin material older than ~ 0.02 Ma (15). As phylogenetically informative ancient protein sequences have been retrieved beyond the limits of aDNA preservation in Eurasia (16–18), we attempted to recover them”. ↩ ↩

    4. 17d.

      Section Introduction:  “The four hominin fossils analyzed (SK 830, 835, 850, and 14132) originated from Swartkrans cave”.  “The teeth are from the oldest deposits at Swartkrans, Member 1 (MB1), which is dated to between 1.8 and 2.2 Ma”.  “Although Swartkrans has produced the largest collection of specimens attributed to P. robustus”. ↩ ↩ ↩

    5. 17e.

      Section Results:  “A total of 425 amino acid positions were consistently identified in all four Paranthropus specimens”. ↩

    6. 17f.

      Section Results:  “all samples show advanced rates of diagenetically-induced amino acid modifications”. ↩ ↩

    7. 17g.

      Section Results:  “Specimens SK 850 and SK 835 were unambiguously identified as male Paranthropus individuals based on the observation of multiple overlapping AMELY-specific peptides”.  “we apply this approach to 11 modern human enamel specimens, achieving sex attribution with 100% accuracy”. ↩

    8. 17h.

      Section Results:  “Based on these phylogenetically informative sites, all four Paranthropus protein sequences appear closer to those in the Homo clade than to any other primate (Figs. S12, S13-24).”  “Given the limited total number of informative sites, conclusive phylogenetic results will require broader sequence coverage. Out of the 16 identified single amino acid polymorphisms, only two, i.e. COL17A1-636 and ENAM-137, showed an allelic state different from that of present-day humans, Neanderthals, and Denisovans.” ↩ ↩ ↩ ↩ ↩ ↩

    9. 17i.

      Section Discussion:  “Due to a single SAP (ENAM–137), our reconstructed trees (Fig. S13-S24) suggest that one of the Paranthropus individuals (SK 835) might be more distantly-related to the other three individuals.” ↩

    10. 17j.

      Section Discussion:  “Regardless, as the small-crowned SK 835 is now confidently assigned to a male, sexual dimorphism is an insufficient explanation for the observed variation within our Paranthropus sample set.” ↩

    11. 17k.

      Section Discussion:  “The four specimens we analyzed, along with other fossils from Swartkrans Member 1, were not accurately mapped when they were collected, thus they come from sediments accumulating within a 500 ka time window.” ↩

  18. 18.

    Line, Peter.  “Fossil evidence for alleged apemen—Part 2:  non-Homo hominids.”  Journal of Creation 19(1):33–42.  2005.  A young-earth survey of every hominin species outside Homo, by a creationist writer who has published widely on human fossils.  It argues from the mainstream literature that all of them were extinct apes, and it has a section on the robust australopiths.

    1. 18a.

      Section The robust australopithecines:  “From the skulls of these creatures, it is obvious that there was nothing human-like about them.” ↩

    2. 18b.

      Section Australopithecus aethiopicus:  “The morphology of the Black Skull has many similarities to that of a small male gorilla, and so it is possible that gorillas and aethiopicus belong to the same biblical kind.” ↩ ↩ ↩ ↩

    3. 18c.

      Section Conclusion:  “The morphological features of the hominid fossils assigned to taxa outside the genus Homo indicate they were mere extinct apes. A species is not equivalent to a biblical kind, and several of the non-Homo hominids may just represent variation within one or more ape kinds”. ↩ ↩

    4. 18d.

      Section Conclusion:  “I suppose this is why evolutionists like the word parallel so much, as in parallel evolution. Call it what you like, but is it science?” ↩ ↩

  19. 19.

    Wood, Todd Charles.  “Baraminological Analysis Places Homo habilis, Homo rudolfensis, and Australopithecus sediba in the Human Holobaramin.”  Answers Research Journal 3:71–90.  May 5, 2010.  The first statistical test of the young-earth claim that fossil hominins divide into human and non-human created kinds.  Wood, a creationist biologist, reanalysed eight published sets of skull and tooth characters by baraminic distance correlation and multidimensional scaling.

    1. 19a.

      Page 71:  “Results indicate that hominins may be divided into as many as four different holobaramins: (1) the genus Homo (including Australopithecus sediba), (2) the genus Paranthropus, (3) Australopithecus africanus, and (4) Gorilla, Pan, Australopithecus afarensis, and Australopithecus garhi.” ↩

    2. 19b.

      Page 72:  “Second, there should be a discontinuity or at least a lack of continuity between the Homo monobaramin and species of the genera Australopithecus and Paranthropus (the so-called robust australopiths).” ↩

    3. 19c.

      Page 73:  “Of the eighteen datasets screened, only Berger et al. (2010); Smith and Grine (2008); Strait, Grine, and Moniz (1997), and both datasets from Strait and Grine (2001; 2004) included more than three species each of Australopithecus/Paranthropus and Homo.”  Page 74:  “All four species of Homo in the dataset share significant, positive BDC, as do the three Paranthropus species.” ↩ ↩

    4. 19d.

      Page 85:  “Based on BDC results alone, the Paranthropus species appear to be a holobaramin, but the MDS results imply that there may be a separation between P. robustus/boisei and P. aethiopicus.”  “The robust australopiths (genus Paranthropus) can be provisionally classified as one holobaramin, and Au. africanus comprises a second potential holobaramin. Au. afarensis and Au. garhi appear to be part of Hartwig-Scherer’s basic type “Gorillinae,” which includes chimpanzees, bonobos, and gorillas.” ↩ ↩ ↩ ↩

  20. 20.

    Hartwig-Scherer, Sigrid.  “Apes or Ancestors?  Interpretations of the Hominid Fossil Record Within Evolutionary & Basic Type Biology.”  Mere Creation:  Science, Faith & Intelligent Design, 212–235.  InterVarsity Press.  Edited by William A. Dembski.  1998.  A German creationist biologist's account of the primate and hominin fossils as the diversification of separately created "basic types", groups defined by the ability to hybridise.  It is the main young-earth treatment that places all the australopiths, robust ones included, in a single created kind.

    1. 20a.

      Page 216:  “A given set of species belong to a basic type if they are connected directly or indirectly through hybridization. Hybridization data are available only for limited cases. In other cases supplementary membership criteria, such as morphological, behavioral or ontogenetic evidence, have to be used. For fossils, the morphological data base is the only evidence available.” ↩

    2. 20b.

      Page 223:  “The ancestral form of the basic type Australopithecinae may have displayed arboreal as well as bipedal locomotor abilities, had mainly unique cranial and facial traits and possessed a brain larger than extant apes of its body size. It is expected that during the radiation of the basic type, different species increased different trends to different degrees. Some have expanded the arboreal trend to the expense of the bipedal activities, others the brain size, or exceeded the special australopithecine traits such as dished faces and megadontia (A. robustus, A. boisei, A. arethiopicus).”  "arethiopicus" is the book's misprint for aethiopicus. ↩ ↩ ↩ ↩

  21. 21.

    Mongle, Carrie S. et al.  “New fossils reveal the hand of Paranthropus boisei.”  Nature 647:944–951.  Oct 15, 2025.  The description of KNM-ER 101000, a partial P. boisei skeleton from Koobi Fora found in 2019–2021, whose hand and foot bones came with teeth and jaw that identify the species.  It is the first hand that can be assigned to P. boisei with confidence, sixty-six years after the species was named.

    1. 21a.

      Section Abstract:  “When Mary Leakey discovered the OH 5 cranium of Paranthropus boisei alongside Oldowan stone artefacts, it was declared “the oldest yet discovered maker of stone tools”1. Whether Paranthropus made and used tools has been debated ever since2–4, largely because there are no known hand bones that can be definitively attributed to this genus.” ↩ ↩

    2. 21b.

      Section Abstract:  “Here we report fossil hand and foot bones unambiguously associated with craniodental material of P. boisei. KNM-ER 101000 demonstrates that P. boisei shared key manipulative and bipedal adaptations with the genus Homo. Moreover, the hand morphology of KNM-ER 101000 converges on that of gorillas in ways that are consistent with manual food processing and would have facilitated powerful grasping, such as that used in climbing.” ↩ ↩ ↩

    3. 21c.

      Section Abstract:  “These fossils suggest that P. boisei was capable of tool making and use in some capacity while also supporting the proposed dichotomy of distinct dietary adaptations between Paranthropus and Homo.” ↩

    4. 21d.

      Section Main text, geological context:  “On the basis of this information, KNM-ER 101000 is estimated to be slightly older than 1.52 million years.” ↩ ↩

    5. 21e.

      Section Main text, hand:  “KNM-ER 101000 indicates that P. boisei had essentially modern human-like intrinsic hand proportions. That is, the thumb was long relative to the palm and other fingers”. ↩ ↩ ↩ ↩

    6. 21f.

      Section Main text, hand:  “a characteristic also exhibited by known species of Australopithecus but not Ardipithecus ramidus”. ↩

    7. 21g.

      Section Main text, foot:  “pedal morphology in KNM-ER 101000 evinces a greater commitment to terrestriality than in earlier hominins”. ↩ ↩

  22. 22.

    Rupe, Christopher, and John Sanford.  Contested Bones.  FMS Publications.  2017.  A young-earth book on the hominin fossils by a geologist and a geneticist, arguing that most fossils are either human or ape.  Quotations are from the first edition;  a second edition appeared in 2019.

    1. 22a.

      Page 161, Figure 2 caption:  “At the time, the fossil was widely promoted to the public as the oldest human ancestor. It was thought that the stone tools found nearby were made by Zinj. This interpretation was retracted shortly thereafter with the discovery of Homo habilis (aka “Handy Man").” ↩ ↩ ↩

    2. 22b.

      Page 162:  “Why didn’t the Leakey’s consider the obvious possibility that the stone tools were manufactured and used by Homo sapiens or Erectus (as opposed to Habilis)?”  “In 1960 an anatomically modern human foot (OH 8) was recovered from Bed I (which was assumed to belong to Habilis).”  Rupe and Sanford also cite the OH 35 leg bones and, on page 240, the OH 86 finger bone. ↩

    3. 22c.

      Page 161:  “Zinj is now universally recognized by the paleoanthropological community to be a robust australopithecine.”  “Zinj has since been appropriately reclassified as Paranthropus boisei (alternatively Au. boisei), an extinct ape far removed from the lineage of man.” ↩

  23. 23.

    Leakey, L. S. B. et al.  “Age of Bed I, Olduvai Gorge, Tanganyika.”  Nature 191:478–479.  Jul 29, 1961.  Potassium-argon dates on volcanic layers at the three Bed I hominin sites, including the OH 5 site, by two Berkeley geochronologists working with Leakey.  It moved the Olduvai hominins from a few hundred thousand years to nearly two million on the standard scale.

    1. 23a.

      Page 479:  “It is to be noted that the hominid-site dates fail to fall in the proper relative order but all are between 1·6 and 1·9 million years. At the present time, the best estimate that we can make of the age of these sites is the average of the several ages, that is, 1·75 million years.” ↩ ↩ ↩ ↩

  24. 24.

    Walter, Robert C. et al.  “Laser-fusion 40Ar/39Ar dating of Bed I, Olduvai Gorge, Tanzania.”  Nature 354:145–149.  Nov 14, 1991.  Argon-argon dates on single volcanic crystals from Olduvai Bed I, the layer that holds OH 5, with Garniss Curtis of the 1961 team among the authors.

    1. 24a.

      Section Abstract:  “These dates reveal that the fossiliferous deposits of middle to upper Bed I, a period of significant biological and climatic change, comprise an extremely brief interval of time, from 1.80 Myr to 1.75 Myr.” ↩ ↩ ↩ ↩

  25. 25.

    Herries, Andy I. R. et al.  “Contemporaneity of Australopithecus, Paranthropus, and early Homo erectus in South Africa.”  Science 368(6486):eaaw7293.  2020.  The description and dating of two skulls from Drimolen, one P. robustus and one early Homo erectus, by uranium-lead dating of flowstones, uranium-series ESR on teeth and palaeomagnetism.  It shows the two genera at the same South African site about two million years ago.

    1. 25a.

      Section Abstract:  “At ~2.04 million to 1.95 million years old, DNH 152 represents the earliest definitive occurrence of Paranthropus robustus, and DNH 134 represents the earliest occurrence of a cranium with clear affinities to Homo erectus These crania also show that Homo, Paranthropus, and Australopithecus were contemporaneous at ~2 million years ago.”  The age comes from uranium-lead dating of the flowstones below and above the fossil-bearing fill, uranium-series ESR dating of a tooth next to the skull, and the reversed and normal magnetic polarity of the sediments, which places the fill near the start of the Olduvai subchron. ↩ ↩ ↩ ↩

  26. 26.

    The factors divide each age by the time since the Flood.  On Creation Ministries International's "some 4,500 years",35 1,400,000 / 4,500 = 311 for the youngest East African P. boisei and 3,000,000 / 4,500 = 667 for the oldest Nyayanga deposits;  OH 5 at 1,750,000 gives 389;  the youngest South African P. robustus, 960,000, gives 213.  Hardy and Carter's earliest Flood, 3386 BC, is 5,411 years before 2026,36 giving 1,400,000 / 5,411 = 259 and 3,000,000 / 5,411 = 554.  A factor is an average over the whole time since the Flood;  if the speed-up lasted only part of that time it had to be larger. ↩ ↩

  27. 27.

    Martin, Jesse M. et al.  “Drimolen cranium DNH 155 documents microevolution in an early hominin species.”  Nature Ecology & Evolution 5:38–45.  Nov 9, 2020.  The description of DNH 155, the most complete male P. robustus skull, from Drimolen.  Comparing it with the female DNH 7 from the same deposit and with younger Swartkrans skulls, the authors argue that differences once put down to sex are change over time within one species.

    1. 27a.

      Section Abstract:  “The most complete known skull of this species is DNH 7 from Drimolen Main Quarry, which differs from P. robustus specimens recovered elsewhere in ways attributed to sexual dimorphism. Here, we describe a new fossil specimen from Drimolen Main Quarry, dated from approximately 2.04–1.95 million years ago, that challenges this view. DNH 155 is a well-preserved adult male cranium that shares with DNH 7 a suite of primitive and derived features unlike those seen in adult P. robustus specimens from other chronologically younger deposits.”  “This represents the most highly resolved evidence yet of microevolutionary change within an early hominin species.” ↩ ↩ ↩

  28. 28.

    Prabhat, Anjali M. et al.  “Homoplasy in the evolution of modern human-like joint proportions in Australopithecus afarensis.”  eLife 10:e65897.  2021.  A comparison of upper- and lower-limb joint sizes in apes, humans and 16 fossil hominin partial skeletons, sorting each species with the more ape-like or more human-like pattern.

    1. 28a.

      Section Abstract:  “Here, we find the limb joint proportions of Australopithecus afarensis, Homo erectus, and Homo naledi to resemble those of modern humans, whereas those of A. africanus, Australopithecus sediba, Paranthropus robustus, Paranthropus boisei, Homo habilis, and Homo floresiensis are more ape-like.” ↩

  29. 29.

    Spoor, Fred et al.  “Implications of early hominid labyrinthine morphology for evolution of human bipedal locomotion.”  Nature 369:645–648.  1994.  A CT study of the semicircular canals, the inner-ear organs that sense head rotation, in living primates and fossil hominins.  Their size and shape track how an animal moves.

    1. 29a.

      Section Abstract:  “Among the fossil hominids the earliest species to demonstrate the modern human morphology is Homo erectus. In contrast, the semicircular canal dimensions in crania from southern Africa attributed to Australopithecus and Paranthropus resemble those of the extant great apes.” ↩

  30. 30.

    The mixing line runs from about −12 per mil for a pure C3 diet to about +2 per mil for a pure C4 diet, the end members Cerling and colleagues use.13  The fraction of C4 is (δ13C − (−12)) / (2 − (−12)).  For the P. boisei mean of −1.3 per mil that is 10.7 / 14 = 0.76, which the paper reports as 77 ± 7 percent.  The range of individual teeth, −3.4 to +0.7, gives 0.61 to 0.91. ↩

  31. 31.

    Green, Daniel R. et al.  “Eighteen million years of diverse enamel proteomes from the East African Rift.”  Nature 643:712–718.  Jul 9, 2025.  A mass-spectrometry search for protein fragments inside the enamel of Turkana Basin fossils from the Pleistocene back to the Oligocene.  It recovered fragments from 16- and 18-million-year-old rhinoceros and elephant-relative teeth and tested how preservation changes with the age of the site.

    1. 31a.

      Page 712:  “we recover fragments of enamelin, ameloblastin, matrix metalloprotease-20 and dentin matrix acidic phosphoprotein 1 from an Early Miocene rhinocerotid and several proboscideans collected from the sites of Buluk (16 million years ago; Ma) and Loperot (18 Ma). Diagenetiform counts decline in progressively older fossils, and we observe variability in Early Miocene preservation across sites.” ↩

    2. 31b.

      Page 716:  “A linear mixed-effects model testing the effects of site age on mass-standardized diagenetiform counts shows a clear decline of counts per fossil specimen over time for putative diagenetiforms (β = −0.05 counts mg−1 Ma−1, s.e. = 0.002, P < 0.001).”  “but not in high-confidence diagenetiforms, perhaps owing to low sample numbers (Supplementary Text).” ↩ ↩

  32. 32.

    Sinclair, P., and Todd Charles Wood.  “Revising Hominin Baraminology with Medoid Partitioning and Fuzzy Analysis.”  Answers Research Journal 14:451–462.  2021.  A rerun of Wood's 2010 skull-and-tooth data with standard cluster methods, done in answer to criticism of baraminology's statistics, and a test on a larger 391-character data set.

    1. 32a.

      Page 453:  “In all eight distance correlation analyses of the Berger et al. (2010) character set (fig. 3), all taxon pairs within the first cluster ( Homo sensu lato ) and within the third cluster ( Paranthropus ) shared significant, positive distance correlation.” ↩

    2. 32b.

      Page 455:  “We removed the Paranthropus taxa from the character set because they consistently formed a distant cluster, and there is no controversy over the conclusion that these taxa are not human.” ↩

  33. 33.

    Wood, Todd Charles, and Peter S. Brummel.  “Hominin Baraminology Reconsidered with Postcranial Characters.”  Proceedings of the Ninth International Conference on Creationism, 251–266.  Edited by J. H. Whitmore.  2023.  A baraminology analysis of 239 new characters from the skeleton below the skull, for fourteen taxa, the first test of the creationist hominin groupings on the body rather than the skull.

    1. 33a.

      Page 252:  “Our taxa include extant chimpanzees, gorillas, and humans, fossil taxa representing seven members of Homo (H. erectus sensu lato, H. floresiensis, H. georgicus, H. habilis, H. heidelbergensis, H. naledi, H. neanderthalensis), three members of Australopithecus (Au. afarensis, Au. africanus sensu lato, Au. sediba), and Ardipithecus ramidus.” ↩

  34. 34.

    O'Micks, J.  “Likely Discontinuity Between Humans and Non-Human Hominins Based on Endocranial Volume and Body Mass With a Special Focus on Homo naledi:  A Short Analysis.”  Answers Research Journal 10:241–243.  2017.  A short creationist analysis that clusters fourteen hominin species by average brain volume and body mass.  It is a crude measure, two numbers per species.

    1. 34a.

      Section Results:  “The second cluster is made up of Homo habilis, Homo naledi, Australopithecus sediba, Australopithecus africanus, Australopithecus afarensis, Paranthropus boisei, Paranthropus aethiopicus, and Ardipithecus ramidus.” ↩

  35. 35.

    “What date would you like?”  Creation 45(2):10.  Apr 2023.  An unsigned news item in Creation Ministries International's magazine about the South African cave dates.  It states plainly where the ministry places the australopith caves in time.

    1. 35a.

      Paragraph 2:  “The caves formed late in Noah’s Flood some 4,500 years ago. The remains of these apish primates at Sterkfontein (australopithecines) were interred after the Flood after the animals had dispersed into the area from the Middle East.” ↩ ↩

  36. 36.

    Hardy, Chris, and Robert Carter.  “The biblical minimum and maximum age of the earth.”  Journal of Creation 28(2):89–96.  2014.  A young-earth paper that works out the earliest and latest dates the biblical numbers allow for creation and the Flood, across the Masoretic, Samaritan and Septuagint texts.

    1. 36a.

      Page 96:  “The Flood probably occurred between 2600 bc and 2300 bc, but certainly between 3386 bc and 2256 bc (table 5).” ↩ ↩

  37. 37.

    Baumgardner, John R.  101 Questions and Answers Concerning Catastrophic Plate Tectonics.  Self-published.  Apr 2012.  The author of catastrophic plate tectonics answers questions put by reviewers of young-earth Flood models.  This article uses only his split of radioactive decay between Creation Week and the Flood.

    1. 37a.

      Section Q76:  “This first episode accounts for up to as much as roughly 3.7 billion years' worth (at presently observed rates) of nuclear decay products in the earth's pre-Flood rocks.”  “Among the lines of evidence for up to about 600 million years' worth of nuclear decay (at presently observed rates) during the Flood cataclysm, are the presence of abundant radiohalos, both from uranium and polonium, as well as high concentrations of fission tracks in crystals in volcanic tuffs and in granitic rocks”. ↩

  38. 38.

    Oard, Michael J.  “Much Greater Cosmic Rays During the Ice Age and Before.”  Creation Research Society Quarterly 58(1):30–48.  2021.  The fullest young-earth treatment of cosmogenic dating, by a prolific young-earth writer on the Ice Age.  On burial dating it concedes that accelerated decay must have continued after the Flood.

    1. 38a.

      Page 39:  “But, secular scientists find values around three or four. Such a ratio implies hundreds of thousands to a few million years of age. This means that much accelerated radiometric decay has taken place after the Flood.” ↩