Dietary change among hominins and cercopithecids in Ethiopia during the early Pliocene

Self Cite

Recent discoveries of multiple middle Pliocene hominins have raised the possibility that early hominins were as speciose as later hominins. However, debates continue to arise around the validity of most of these new taxa, largely based on poor preservation of holotype specimens, small sample size, or the lack of evidence for ecological diversity. A closer look at the currently available fossil evidence from Ethiopia, Kenya, and Chad indicate that Australopithecus afarensis was not the only hominin species during the middle Pliocene, and that there were other species clearly distinguishable from it by their locomotor adaptation and diet. Although there is no doubt that the presence of multiple species during the middle Pliocene opens new windows into our evolutionary past, it also complicates our understanding of early hominin taxonomy and phylogenetic relationships.If one looks back over the controversies of human evolution, they have one element in common: new discoveries, theories, methods came along which no one in the controversy anticipated. The "facts" changed, and consequently people were not right or wrong in any simple way.S. L. Washburn and R. L. Ciochon, 1974 (1) New fossil discoveries and analytical methods that have proliferated during the last few decades have fundamentally changed how we study and interpret hominin fossils and understand human evolution. The discovery and subsequent naming of Australopithecus afarensis in the late 1970s was one of the major milestones in paleoanthropology (2). Its discovery not only pushed the record of hominins to earlier than 3 million years ago (Ma) (2), but also demonstrated the antiquity of human-like bipedality (3). However, the taxonomic homogeneity of the Au. afarensis hypodigm has been questioned since its naming (4-7), even though the Hadar fossil sample appears to be no more variable than other living ape species (8-11). A consensus emerged during the 1980s in which Au. afarensis, dated to between 3.7 and 2.9 Ma, was considered to be the sole early hominin species older than 3 Ma, largely supported by the lack of fossil evidence to indicate otherwise.When Australopithecus bahrelghazali was named in 1995 based on an approximately 3.5-Ma partial mandible from Chad (12), it was quickly dismissed as a geographic variant of Au. afarensis (13-15). The initial descriptions of Ardipithecus ramidus (16) and Australopithecus anamensis (17), followed by the naming of even earlier hominin species, such as Orrorin tugenensis (18), Ardipithecus kadabba (19,20), and Sahelanthropus tchadensis (21), extended the antiquity of our lineage as far back as >6 Ma. These early hominins initially appeared to show no temporal or spatial overlap, and hence reinforced the idea that the early phases of hominin evolution were characterized by phenetic continuity and phyletic gradualism, with only one hominin species existing in a region at any given time >3 Ma (e.g., ref. 22; see discussions below).The discovery of the Burtele partial foot from Ethiopia (23), the naming of Kenyan...

Section: Pliocene Hominin Diversity Sympatry and The Question Of Nimentioning

confidence: 99%

Section: Pliocene Hominin Diversity Sympatry and The Question Of Nimentioning

confidence: 99%

The Pliocene hominin diversity conundrum: Do more fossils mean less clarity?

Haile‐Selassie

Melillo

2016

Self Cite

“…Increasing aridity has been thought to drive the origin and subsequent expansion of C 4 plants (grasses and sedges) (22). The long-term increase in the abundance of C 4 plants throughout the Pliocene and Pleistocene has been well documented in eastern Africa using carbon isotope ratios in pedogenic carbonates and leaf wax biomarkers (23,24) and coincides with an increasing reliance on C 4 -based resources among mammals, including hominins and other primates (25,26). Variation in the timing of vegetation change across basins indicates that existing continental-and regional-scale climate records are not sufficient to understand the drivers of basin-and local-scale ecological change, and do not reflect local hominin environments (23,27).…”

mentioning

confidence: 99%

Aridity and hominin environments

Blumenthal

Levin

Brown

et al. 2017

Self Cite

145

Aridification is often considered a major driver of long-term ecological change and hominin evolution in eastern Africa during the Plio-Pleistocene; however, this hypothesis remains inadequately tested owing to difficulties in reconstructing terrestrial paleoclimate. We present a revised aridity index for quantifying water deficit (WD) in terrestrial environments using tooth enamel δ18O values, and use this approach to address paleoaridity over the past 4.4 million years in eastern Africa. We find no long-term trend in WD, consistent with other terrestrial climate indicators in the Omo-Turkana Basin, and no relationship between paleoaridity and herbivore paleodiet structure among fossil collections meeting the criteria for WD estimation. Thus, we suggest that changes in the abundance of C4 grass and grazing herbivores in eastern Africa during the Pliocene and Pleistocene may have been decoupled from aridity. As in modern African ecosystems, other factors, such as rainfall seasonality or ecological interactions among plants and mammals, may be important for understanding the evolution of C4 grass- and grazer-dominated biomes.

“…However, extensive isotopic data from Plio-Pleistocene hominin teeth provide a clear picture of diets in different lineages, temporal trends, and dietary niche partitioning between Pleistocene genera (91)(92)(93)(94)(95)(96). Two early species (4.4-4 Ma), Ardipithecus ramidus and Australopithecus anamensis, are anomalous for their C 3 -dominated diets (−11.6‰ to −8.5‰).…”

mentioning

confidence: 99%

Neogene biomarker record of vegetation change in eastern Africa

Uno

Polissar

Jackson

et al. 2016

126

103

The evolution of C4 grassland ecosystems in eastern Africa has been intensely studied because of the potential influence of vegetation on mammalian evolution, including that of our own lineage, hominins. Although a handful of sparse vegetation records exists from middle and early Miocene terrestrial fossil sites, there is no comprehensive record of vegetation through the Neogene. Here we present a vegetation record spanning the Neogene and Quaternary Periods that documents the appearance and subsequent expansion of C4 grasslands in eastern Africa. Carbon isotope ratios from terrestrial plant wax biomarkers deposited in marine sediments indicate constant C3 vegetation from ∼24 Ma to 10 Ma, when C4 grasses first appeared. From this time forward, C4 vegetation increases monotonically to present, with a coherent signal between marine core sites located in the Somali Basin and the Red Sea. The response of mammalian herbivores to the appearance of C4 grasses at 10 Ma is immediate, as evidenced from existing records of mammalian diets from isotopic analyses of tooth enamel. The expansion of C4 vegetation in eastern Africa is broadly mirrored by increasing proportions of C4-based foods in hominin diets, beginning at 3.8 Ma in Australopithecus and, slightly later, Kenyanthropus. This continues into the late Pleistocene in Paranthropus, whereas Homo maintains a flexible diet. The biomarker vegetation record suggests the increase in open, C4 grassland ecosystems over the last 10 Ma may have operated as a selection pressure for traits and behaviors in Homo such as bipedalism, flexible diets, and complex social structure.