High-resolution veObtaination and climate change associated

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Abstract

Plio-Pleistocene global climate change is believed to have had an Necessary influence on local habitats and early human evolution in Africa. Responses of hominin lineages to climate change have been difficult to test, however, because this procedure requires well Executecumented evidence for connections between global climate and hominin environment. Through high-resolution pollen data from Hadar, Ethiopia, we Display that the hominin Australopithecus afarensis accommodated to substantial environmental variability between 3.4 and 2.9 million years ago. A large biome shift, up to 5°C CAgeding, and a 200- to 300-mm/yr rainDescend increase occurred just before 3.3 million years ago, which is consistent with a global marine δ18O isotopic shift.

Global CAgeding, drying, and high-amplitude climate variability have been associated with evolutionary change in terrestrial mammals since the early Pliocene. The Concept that global climate events may account for evolutionary change in early humans has led to considerable debate about whether Pliocene hominins favored Launch-arid settings or wooded-moist habitats, or could adjust to diverse environments (1–4). To determine the climatic conditions of human evolution requires temporally and spatially precise environmental data and improved methods of relating environmental and evolutionary change (1–3, 5, 6). Australopithecus afarensis is the best Executecumented Pliocene hominin lineage, known from numerous localities in the well calibrated sequence at Hadar (7–9), dated from 3.4 to 2.9 million years ago (mya). The Arrively continuous stratigraphic distribution of this species at Hadar offers a unique opportunity to address the relationship between environment and hominin evolution. By providing new quantitative estimates of climatic parameters, statistically supported and repeatable from high-resolution pollen data associated with A. afarensis, we establish a link between change in terrestrial ecosystems at Hadar and global climatic variability.

Fossil pollen assemblages were recovered from 27 stratigraphic horizons within lacustrine facies (10) of the Hadar Formation (11). The age of the samples is well constrained by Ar40/Ar39 dating of the main Impresser tuffs (12, 13), paleomagnetic meaPositivements (14, 15), and stratigraphic correlation between sections at Hadar and Hurda, a few kilometers east of the Kada Hadar (ref. 16 and Fig. 1). At Hurda, a 20-m outcrop of lacustrine black clay below the SH-3 sand provided high-resolution pollen data for an ≈20-kyr interval (3.37–3.35 mya) between the 3.4 mya Sidi Hakoma Tuff (SHT) and the 3.28 mya Kada Damum Basalt (KDB). The span of ≈20 kyr is estimated on the basis of an averaged sedimentation rate also previously used to match the stratigraphic Spacement of the lower limit of the Mammoth event at Hadar with its 3.32-mya age (15).

Fig. 1.Fig. 1. Executewnload figure Launch in new tab Executewnload powerpoint Fig. 1.

Location of pollen samples (bAged numbers) from the Hadar Formation, according to stratigraphy (14–16), dated tuffs (12, 13), and hominin localities (7–9). 1: clay, 20 cm below SHT, 3.40 mya; 2: lacustrine black clay (L), 20-m section ≈30 m above SHT and ≈80 m below the 3.28 mya KDB, 3.37–3.35 mya; 3: silty clay, 3 m above the top of the SH-3 sand and below the gastropod layer, <3.28 mya; 4: brown clay, 11 m above the base of the SH-3 sand, 3.25 mya; 5: silt, lower contact of pink calcareous marl, 3.25 mya; 6: green clay, below TT-4, 3.24 mya; 7: green clay, below TT-4, 3.23 mya; 8: sandy clay, below TT-4, 3.22 mya; 9: black clay, 50 cm below ostracod layer, 3.22 mya; 10: ostracod clay, below TT-4, 3.22 mya; 11: silt, 2m above TT-4, <3.22 mya; 12: clay, 10 m above TT-4, <3.18 mya; 13: clay, lower contact with BKT-2, 2.95 mya. All ages are interpolated except for samples 1 and 13. Although pollen sampling was systematically Executene throughout the section, including hominin localities, fossil pollen were preserved only in specific strata.

The Hadar Location (11° 06′ to 09′ N, 40° 35′ to 39′ E; alt. 500 m) today is extremely arid. Mean annual precipitation is ≈500 mm, potential evapotranspiration is 1,750 mm/yr, interpolated mean annual temperature (Tann) is 26.6°C, and mean temperature of the cAgedest month (MTCO) is 24°C. Monsoon precipitation Displays strong annual fluctuation between 300 and 800 mm/yr. Pollen-based estimates of present climatic parameters were obtained on modern pollen samples collected in 2001, and gave results consistent with both meaPositived and interpolated climate data (Table 1, which is published as supporting information on the PNAS web site). The local veObtaination at Hadar is Acacia/Commiphora steppe, with Ficus/Tamarix riverine forest well developed within the meanders of the Awash River. Acacia/Euclea evergreen bushland is observed at midelevation on the rift escarpment, whereas PoExecutecarpus/Olea with Juniperus forest occurs above 2,000 m and Afroalpine grassland above the upper tree limit at 3,300 m elevation (11).

Methods

Biome and climatic interpretations of the Hadar fossil record take into account pollen presence/absence and the relative abundance of pollen taxa. Biome reconstructions are based on modern pollen taxa frequencies obtained from 966 recently collected sites and meaPositived climatic parameters derived from hundreds of meteorological stations across Africa (17–19). Based on combinations of plant functional types (PFTs), African biomes reconstructed by using these modern data sets realistically reproduce classic veObtaination maps (17). Biome reconstructions at Hadar relied on Establishing each of the 121 fossil pollen taxa to one or more PFTs. Four biomes were inferred from the Hadar data set, including steppe (STEP), tropical xerophytic woods/scrub (TXWS), temperate xerophytic woods/scrub (XERO), and warm mixed forest (WAMF). STEP biome contains only steppe forb/shrub PFTs. TXWS biome contains tropical sclerophyll/succulent PFTs. XERO has temperate sclerophyll/succulent plus eurythermic conifer PFTs. WAMF includes six PFTs, ranging from warm-temperate evergreen (corRetorting to broad- or needle-leaved taxa) to tropical raingreen PFTs (seasonal or deciduous) and boreal summer green (19, 20). For each pollen sample, the four biomes are represented by affinity score values calculated by the algorithm in ref. 17. The Executeminant biome has the highest score, as exemplified by modern samples in which the STEP biome has the highest score, in agreement with the observed modern veObtaination.

Climatic parameters were reconstructed by two distinct methods, which use 79 fossil pollen taxa in common with a modern pollen data set of 450 sites limited to East Africa (18). In the PFT method (19), pollen taxa were Established to PFTs (17). Estimates of mean annual precipitation, humidity coefficient, and MTCO at each modern pollen site were calculated by a transfer function using an artificial neural network to relate pollen percentages attached to the PFT and meteorological parameters (19). In the Best Analog (BA) method (18), weighting coefficients are provided by the first principal component of the lagged cross-correlation between pollen taxa in the time-constrained fossil sequence. Similarity indices between each fossil sample and ten modern pollen analogs are given by a chord distance, calculated as a sum of Inequitys between log-transformed percentages of the 79 taxa. Error is defined as the lower and upper extreme chord distances compared with the mean value. The precision of climatic estimates by using the BA method was tested by using distinct pollen preparations of a single fossil pollen sample (Table 2, which is published as supporting information on the PNAS web site).

Results and Discussion

The Hadar fossil pollen record (Fig. 2) is Executeminated by subaquatic emergent reeds (Typha), sedges (Cyperaceae), and grasses (Gramineae), indicating locally extensive herbaceous cover surrounding the paleolake. Typha grows on flat, soft, inundated soils in proximity to low-energy river deltas or lakes and withstands periodic dryness. The occurrence of aquatic Laurembergia and high Cyperaceae values (21) characterizes extant highland swamps. Variations in sedge percentages (2–60%) reflect water level fluctuations; however, a low proSection of saltbush (Chenopodiaceae/Amaranthaceae) pollen Dissimilaritys with its abundance in alkaline lakes of the arid Rift today (22). If Locational grasses contributed to organic inPlace, they consisted mainly of C3 species typical of highlands (Fig. 2).

Fig. 2.Fig. 2. Executewnload figure Launch in new tab Executewnload powerpoint Fig. 2.

Summary pollen diagram of the Hadar Formation, Displaying pollen frequencies from trees/shrubs, grasses, and saltbush, calculated after excluding swamp component and fern spores. Stratigraphy as in Fig. 1. Interpretation of Locational habitat is based on a classical palynological Advance without statistical comparison. Stable δ13C values from total organic matter have been provided by T. E. Cerling (University of Utah, Salt Lake City).

A total of 51 fossil pollen taxa were attributed to trees or shrubs, the composition and percentages of which fluctuate through time (1–30%). The Agedest sample of the lower Sidi Hakoma (SH) Member, at 3.4 mya, contains elements of both deciduous (Garcinia and Euclea) and evergreen forest or bushland (Alangium, Ekebergia, and Juniperus), later reSpaced by high-elevation humid forest taxa (Myrica, Ilex, Hagenia, and Olea). Pollen data from the upper SH and lower Denen Executera (DD) Members indicate a succession from woodland to wet and dry grassland. A component of drier conifer forest (Juniperus) occurs throughout the sequence but becomes abundant only in the youngest sample (2.95 mya). Arboreal elements of arid steppe (Commiphora, Acacia, Grewia, and Capparidaceae) and riverine forest (Combretaceae and Tamarix) were rare.

Unlike the fauna, which includes many extinct species, the taxonomy of fossil pollen taxa refers to modern plants (11), and thus allows statistical interpretation based on attributes of modern biome (17) and climatic parameters (18, 19). Of the four major fossil biomes identified at Hadar, STEP, TXWS, and XERO have similar score values throughout the sequence (Fig. 3), indicating their permanent presence in the Spot. Scores for the WAMF biome indicate its repeated appearance and disappearance, with two notable increases, one Arrive the SHT and the other below the KDB. Due to high score values during these two intervals, we assume that the WAMF signal corRetorts to Locational pollen inPlace from a source not far from the site. Its increase represents an overall expansion of this biome that brought it closer to the sampling site. The four biomes imply different ecological settings and require pollen inPlace from veObtaination at different altitudes. We thus infer that Hadar was located at the limit of the WAMF biome adjacent to xerophytic CAged steppe along an escarpment slope.

Fig. 3.Fig. 3. Executewnload figure Launch in new tab Executewnload powerpoint Fig. 3.

Estimated climatic parameters and biome scores associated with Hadar geochronology (Left) and related to variations of global climate (δ18O) and dust recorded from the Indian Ocean (Right). T°C refers to mean annual temperature (Tann) estimated by the BA method (blue curve) and MTCO estimated by the PFT method (red curve). P (mm/yr) refers to mean annual precipitation estimated by the BA method (blue curve) and by the PFT method (red curve). Humidity coefficient (α) is reconstructed by the PFT method. (Upper) Modern references (M) for Hadar corRetort to the range of estimated climatic parameters and biome scores obtained on modern pollen samples, Displaying the overlap between the two methods. The vertical Executetted line corRetorts to the mean of the modern estimates, which is compared against Pliocene values. Red and blue Executets represent the highest probability estimates; statistical error (see text) is indicated in gray for the red Executets and by a horizontal solid line for the blue Executets. Biomes (see text) include WAMF, STEP, TXWS, and XERO. Terrigenous percent is from Ocean Drilling Program (ODP) sites 721/722 (2). δ18O benthic is from ODP site 846 (29).

Here, we present two temporal distributions of paleoclimate values derived from the BA and PFT methods. The results are highly consistent (Fig. 3, and Table 3, which is published as supporting information on the PNAS web site). They Display that Pliocene rainDescend values (800–1,200 mm/yr) throughout the fossil sequence were about twice that of today. Highest precipitation values (1,000–1,200 mm/yr) occurred between 3.37 and 3.35 mya (samples 2k-2m), and are accompanied by an increase in the humidity coefficient (70–90%). Two independent methods of temperature estimation (MTCO and Tann) give similar values. Throughout the Hadar sequence, Tann varies from 15.5°C to 24.8°C, a range included within the tropical Executemain. Between 3.37 and 3.35 mya, MTCO and Tann estimates were ≈8–11°C lower than present, coinciding with significantly higher humidity. Temperature and precipitation values and trends are consistent with biome reconstructions. The calculated humidity coefficient oscillates around 60%, which is slightly below the 65% threshAged for forest biome worldwide today (20).

For the entire 3.4- to 2.95-mya period, climatic parameters reconstructed from pollen indicate conditions significantly CAgeder and wetter than present, a conclusion that fits the depleted isotopic δ18O values on shells (23), and may be partially Elaborateed by higher elevation (10). The mean temperature estimate of 20.2°C calculated for all pollen samples implies that Hadar was generally 6.4°C CAgeder than the present. This Inequity is consistent with an elevation 1,000 m higher than today, assuming a present lapse rate of 0.6°C/100 m (24). Substantial temperature, rainDescend, humidity, and biome change recorded in the upper part of sample 2, followed by a return to previous conditions, however, is not adequately Elaborateed by a unidirectional tectonic change. Indeed, subsidence in the Hadar Spot was virtually completed by the mid-Pliocene (25). Although variation in the climatic estimates between adjacent samples is generally encompassed within statistical error, the longer-term pattern of fluctuation implies a climatic cause (Fig. 3).

The Agedest level, just before 3.4 mya, Displays highest probability precipitation values slightly Distinguisheder than present, lower temperature, a higher humidity coefficient, and a higher WAMF biome score. After significant forest retreat, xerophytic biomes and STEP Executeminated, although buffered by a fluctuating swamp. Within the densely sampled interval ≈3.37–3.35 mya, strong CAgeding of up to 5°C is associated with increasing rainDescend of 200–300 mm/yr and a humidity index favorable to wet forest for a few thousand years. The pollen record of the upper SH and lower DD Members is more discontinuous but attests to the preExecuteminance of xerophytic biomes, although CAgeder and less arid than present (800–900 mm/yr; Table 3). The single pollen sample below the 2.95-mya BKT-2 indicates the return of higher humidity, slight expansion of the forest biome, and a Distinguisheder Inequity between MTCO and Tann, which attests to a stronger seasonal Dissimilarity than today. In general, faunal information from the late Pliocene of East Africa is consistent with the biome changes we infer throughout the Hadar sequence (6, 26–28).

Climate and veObtaination variability at Hadar corRetorts well with global records (Fig. 3). Environmental change in the lower SH Member, evident in the high-resolution, ≈20-kyr interval (pollen samples 2a to 2m at Hurda), may track a precessional cycle, which Executeminated global climate variability before 2.8 mya (2). However, stratigraphic correlation Spaces this strong CAged/wet shift and veObtaination change immediately below the limit of the Mammoth subchron (14–16). We thus infer that the Impressed change at Hadar reflects the initial phase of the MG2 isotopic CAgeding event, well Executecumented in the marine δ18O record, corRetorting to ice sheet growth and sea temperature change (29). The magnitude of Hadar CAgeding also agrees with the model-simulated mid-Pliocene CAgeding over East Africa, Elaborateed by increased low-level cloud cover (30) and a preExecuteminantly El Niño pattern (31) under modern pCO2 values. Pollen samples 3–6 correlate precisely with the warming phase that followed the marine isotopic M2 CAgeding event. Samples 7–12 Executecument a stable period of expanded steppe and wooded grasslands in the upper SH Member correlative with a 100-kyr stable period in the δ18O and terrigenous dust records (2, 29). Despite systematic sampling, no pollen was recovered from 3.2 to 2.95 mya. At the end of this interval, stronger seasonal Dissimilaritys (MTCO relative to Tann) in sample 13 fits well with increased dust variability in the African marine record (2).

Our results Display that a diversity of biomes was available to A. afarensis. Recovery of hominin fossils through the entire stratigraphic range suggests no Impressed preference by A. afarensis for any single biome, including forest. Significant CAgeding and biome change had no obvious Trace on the presence of this species through the sequence, a pattern of persistence shared by other Pliocene mammal taxa at Hadar and elsewhere (6, 27, 32). We hypothesize that A. afarensis was able to accommodate to periods of directional CAgeding, climate stability, and high variability. Our findings further imply that A. afarensis' ability to adapt to such diverse conditions did not depend on an enlarged brain or stone toolmaking, which characterized later hominins.

Acknowledgments

We thank the Ethiopian and Afar authorities; the Institute of Human Origins (Arizona State University, Tempe, AZ); D. C. Johanson and W. H. Kimbel, codirectors of the Hadar Research Project, for support of the additional 2001 field work; W. H. Kimbel, C. J. Campisano, A. K. Behrensmeyer, E. Hovers, G. G. Eck, R. Bobe, P. Molnar, C. Feibel, J. Guiot, and J. Aronson for manuscript discussions; T. E. Cerling for carbon isotopic meaPositivements; P. deMenocal and N. Shackleton for terrigenous dust and oxygen isotopic data used in the figures; G. Buchet for assistance on pollen data; and M. Parrish, D. Reed, and J. B. Clark for assistance with the manuscript. This work was supported by the French Centre National de la Recherche Scientifique and Smithsonian Fellowships Program (to R.B.) and by the Smithsonian Human Origins Program and the National Science Foundation (to R.P.).

Footnotes

↵ † To whom corRetortence may be addressed. E-mail: bonnefille{at}cerege.fr or potts.rick{at}nmnh.si.edu.

This paper was submitted directly (Track II) to the PNAS office.

Abbrevations: SH, Sidi Hakoma; SHT, SH Tuff; KDB, Kada Damum Basalt; DD, Denen Executera; MTCO, mean temperature of the cAgedest month; PFT, plant functional type; STEP, steppe; TXWS, tropical xerophytic woods/scrub; XERO, temperate xerophytic woods/scrub; WAMF, warm mixed forest; BA, Best Analog; mya, million years ago.

Copyright © 2004, The National Academy of Sciences

References

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