scholarly journals Arguments that Prehistorical and Modern Humans Belong to the Same Species

Author(s):  
Rainer Kühne

I argue that the evidence of the Out-of-Africa hypothesis and the evidence of multiregional evolution of prehistorical humans can be understood if there has been interbreeding between Homo erectus, Homo neanderthalensis, and Homo sapiens at least during the preceding 700,000 years. These interbreedings require descendants who are capable of reproduction and therefore parents who belong to the same species. I suggest that a number of prehistorical humans who are at present regarded as belonging to different species belong in fact to one single species.  

2019 ◽  
Author(s):  
Rainer Walter Kühne

I argue that the evidence of the Out-of-Africa hypothesis and the evidence of multiregional evolution of prehistorical humans can be understood if there has been interbreeding between Homo erectus, Homo neanderthalensis, and Homo sapiens at least during the preceding 700,000 years. These interbreedings require descendants who are capable of reproduction and therefore parents who belong to the same species. I suggest that a number of prehistorical humans who are at present regarded as belonging to different species belong in fact to one single species.


2005 ◽  
Vol 32 ◽  
pp. 221-232 ◽  
Author(s):  
Harald Haarmann

Since the earliest manifestations of symbolic activity in modern humans (Homo sapiens sapiens) in the Upper Palaeolithic, there is evidence for two independent cognitive procedures, for the production of representational images (naturalistic pictures or sculptures) and of abstract signs. The use of signs and symbols is attested for archaic humans (Homo neanderthalensis) and for Homo erectus while art in naturalistic style is an innovation among modern humans. The symbiotic interaction of the two symbolic capacities is illustrated for the visual heritage of Palaeolithic cave paintings in Southwestern Europe, for rock engravings in the Italian Alps (Val Camonica) and for the vivid use of signs and symbols in Southeastern Europe during the Neolithic. Around 5500 BC, sign use in Southeastern Europe reached a sophisticated stage of organization as to produce the earliest writing system of mankind. Since abstractness is the main theme in the visual heritage of the region, this script, not surprisingly, is composed of predominantly abstract signs.


Author(s):  
Bernard Wood

So when and where in human evolutionary history do we see the earliest evidence of creatures that are more like modern humans? ‘Pre-modern Homo’ considers the species that many hominins researchers are comfortable with recognizing as members of the genus Homo. It looks at the earliest fossil evidence of pre-modern Homo from Africa, and then follows Homo as it moves out of Africa into the rest of the Old World. It begins with Homo ergaster, dated to around 2 mya, and then moves on to Homo erectus, which was found in sites in Africa, China, and Indonesia. Other pre-modern Homo species include Homo heidelbergensis; Homo naledi; Homo floresiensis; and Homo neanderthalensis.


1970 ◽  
Vol 9 (1) ◽  
pp. 169-202
Author(s):  
Jolanta Koszteyn

Within the historical times, which roughly corresponds with the Holocene epoch, the whole of mankind is believed to be a single species. Homo sapiens. But the human genealogical tree (phylogeny) is populated by a really astounding number of paleontological species and paleontological genera: Ardipithecus ramidus, Australopithecus anamensis, Australopithecus afarensis, Australopithecus africanus, Paranthropus robustus, Paranthropus boisei, Homo habilis, Homo georgicus. Homo erectus, Homo ergaster, Homo antecessor, Homo heidelbergensis, Homo neanderthalensis, Homo sapiens. (cf. Gyula 2002). In fact there are many more (Sahelanthropus tchadensis, Orrorin tugenensis, Kenyanthropus platyops, Australopithecus garhi, Australopithecus aethiopicus) but Foley (2002), quite reasonably, states that the evidence for their existence is, at present, insufficient. The existence of these multiple forms is beyond any doubt. The doubt, however arises concerning the human or „prehuman" status of them. Were they really true specific forms, half-way between the apes and Holocene man? Is it possible that they constitute a number of different ecotypes (or paleoraces) within the same natural species of Homo sapiens?


Author(s):  
Francisco J. Ayala ◽  
Camilo J. Cela-Conde

This chapter deals with the similarities and differences between Homo neanderthalensis and Homo sapiens, by considering genetic, brain, and cognitive evidence. The genetic differentiation emerges from fossil genetic evidence obtained first from mtDNA and later from nuclear DNA. With high throughput whole genome sequencing, sequences have been obtained from the Denisova Cave (Siberia) fossils. Nuclear DNA of a third species (“Denisovans”) has been obtained from the same cave and used to define the phylogenetic relationships among the three species during the Upper Palaeolithic. Archaeological comparisons make it possible to advance a four-mode model of the evolution of symbolism. Neanderthals and modern humans would share a “modern mind” as defined up to Symbolic Mode 3. Whether the Neanderthals reached symbolic Mode 4 remains unsettled.


2014 ◽  
Vol 112 (2) ◽  
pp. 366-371 ◽  
Author(s):  
Habiba Chirchir ◽  
Tracy L. Kivell ◽  
Christopher B. Ruff ◽  
Jean-Jacques Hublin ◽  
Kristian J. Carlson ◽  
...  

Humans are unique, compared with our closest living relatives (chimpanzees) and early fossil hominins, in having an enlarged body size and lower limb joint surfaces in combination with a relatively gracile skeleton (i.e., lower bone mass for our body size). Some analyses have observed that in at least a few anatomical regions modern humans today appear to have relatively low trabecular density, but little is known about how that density varies throughout the human skeleton and across species or how and when the present trabecular patterns emerged over the course of human evolution. Here, we test the hypotheses that (i) recent modern humans have low trabecular density throughout the upper and lower limbs compared with other primate taxa and (ii) the reduction in trabecular density first occurred in early Homo erectus, consistent with the shift toward a modern human locomotor anatomy, or more recently in concert with diaphyseal gracilization in Holocene humans. We used peripheral quantitative CT and microtomography to measure trabecular bone of limb epiphyses (long bone articular ends) in modern humans and chimpanzees and in fossil hominins attributed to Australopithecus africanus, Paranthropus robustus/early Homo from Swartkrans, Homo neanderthalensis, and early Homo sapiens. Results show that only recent modern humans have low trabecular density throughout the limb joints. Extinct hominins, including pre-Holocene Homo sapiens, retain the high levels seen in nonhuman primates. Thus, the low trabecular density of the recent modern human skeleton evolved late in our evolutionary history, potentially resulting from increased sedentism and reliance on technological and cultural innovations.


2021 ◽  
Vol 84 (4) ◽  
pp. 487-502
Author(s):  
Robert B. Eckhardt

Abstract Confidence intervals for estimates of human mtDNA sequence diversity, chimpanzee-human mtDNA sequence divergence, and the time of splitting of the pongid-hominid lineages are presented. Consistent with all the data used in estimating the coalescence time for human mitochondrial lineages to a common ancestral mitochondrion is a range of dates from less than 79,000 years ago to more than 1,139,000 years ago. Consequently, the hypothesis that a migration of modern humans (Homo sapiens) out of Africa in the range of 140,000 to 280,000 years ago resulted in the complete replacement, without genetic interchange, of earlier Eurasian hominid populations (Homo erectus) is but one of several possible interpretations of the mtDNA data. The data are also compatible with the hypothesis, suggested earlier and supported by fossil evidence, of a single, more ancient expansion of the range of Homo erectus from Africa, followed by a gradual transition to Homo sapiens in Europe, Asia, and Africa.


Author(s):  
Jan Zalasiewicz ◽  
Mark Williams

It is just the latest of many climate phases of the Quaternary Period. The 103rd major shift in climate-driven global oxygen isotope values, to be precise, since the official-designated beginning of the Quaternary Period, 2.58 million years ago. And, many of those major phases, as we have seen, include dozens of climate oscillations far greater in scale than humans have witnessed since written records began. Nevertheless, it is our warm phase, that within which our civilization has grown, and hence it has been separated as a distinct epoch, the Holocene, a little over 0.01 of a million years long. Its counterpart is the Pleistocene Epoch, in which reside those other 2.57 million years of Quaternary time, and those other 102 major climate oscillations. Thus, we live—at least as far as formal geological nomenclature goes—in a privileged time. When this epoch began, Homo sapiens had already existed for some 150,000 years. As a species its prospects might not have seemed bright: this creature lacked anything terribly impressive in the way of claws or teeth or thick fur or armour. But by being ingenious at developing what one might describe as artificial claws and teeth—axes and spears and arrows—it could kill and eat mammals considerably larger than itself. In those early days, it might not have prospered, exactly, but it clung to existence, seemingly weathering at least one very bad patch, several tens of thousands of years ago, when its numbers dropped almost to extinction levels. It survived the climate oscillations of the late Pleistocene—the droughts and floods and episodes of bitter cold and killing heat—by adapting its behaviour or migrating as best it could. Its migrations from its place of origin, Africa, were on an epic scale. The many thousands of individual and collective stories of hope, fear, endurance, courage, tragedy, and (less commonly) triumph are all lost. What remains is the evidence that humans, by the beginning of the Holocene, had spread widely over Europe and Asia, ousting (it seems) their kindred hominin species, Homo neanderthalensis and Homo erectus.


Hereditas ◽  
2021 ◽  
Vol 158 (1) ◽  
Author(s):  
Úlfur Árnason

Abstract Background The Out of Africa hypothesis, OOAH, was challenged recently in an extended mtDNA analysis, PPA (Progressive Phylogenetic Analysis), that identified the African human populations as paraphyletic, a finding that contradicted the common OOAH understanding that Hss had originated in Africa and invaded Eurasia from there. The results were consistent with the molecular Out of Eurasia hypothesis, OOEH, and Eurasian palaeontology, a subject that has been largely disregarded in the discussion of OOAH. Results In the present study the mtDNA tree, a phylogeny based on maternal inheritance, was compared to the nuclear DNA tree of the paternally transmitted Y-chromosome haplotypes, Y-DNAs. The comparison showed full phylogenetic coherence between these two separate sets of data. The results were consistent with potentially four translocations of modern humans from Eurasia into Africa, the earliest taking place ≈ 250,000 years before present, YBP. The results were in accordance with the postulates behind OOEH at the same time as they lent no support to the OOAH. Conclusions The conformity between the mtDNA and Y-DNA phylogenies of Hss is consistent with the understanding that Eurasia was the donor and not the receiver in human evolution. The evolutionary problems related to OOAH became similarly exposed by the mtDNA introgression that took place from Hss into Neanderthals ≈ 500,000 YBP, a circumstance that demonstrated the early coexistence of the two lineages in Eurasia.


2016 ◽  
Author(s):  
Arturo Tozzi

ABSTRACTWe display a detailed description of mimetic muscles in extinct human species, framed in comparative and phylogenetic contexts. Using known facial landmarks, we assessed the arrangement of muscles of facial expression in Homo sapiens, neanderthalensis, erectus, heidelbergensis and ergaster. In modern humans, several perioral muscles are proportionally smaller in size (levator labii superioris, zygomaticus minor, zygomaticus major and triangularis) and/or located more medially (levator labii superioris, zygomaticus minor and quadratus labii inferioris) than in other human species. As mimetic musculature is examined in the most ancient specimens up to the most recent, there is a general trend towards an increase in size of corrugator supercillii and triangularis. Homo ergaster’s mimetic musculature closely resembles modern Homo, both in size and in location; furthermore, Homo erectus and Homo neanderthalensis share many muscular features. The extinct human species had an elaborate and highly graded facial communication system, but it remained qualitatively different from that reported in modern Homo. Compared with other human species, Homo sapiens clearly exhibits a lower degree of facial expression, possibly correlated with more sophisticated social behaviours and with enhanced speech capabilities. The presence of anatomical variation among species of the genus Homo raises important questions about the possible taxonomic value of mimetic muscles.


Sign in / Sign up

Export Citation Format

Share Document