The Hominin Sites and Paleolakes Drilling Project

. The role that climate and environmental history may have played in inﬂuencing human evolution has been the focus of considerable interest and controversy among paleoanthropologists for decades. Prior attempts to understand the environmental history side of this equation have centered around the study of outcrop sediments and fossils adjacent to where fossil hominins (ancestors or close relatives of modern humans) are found, or from the study of deep sea drill cores. However, outcrop sediments are often highly weathered and thus are unsuitable for some types of paleoclimatic records, and deep sea core records come from long distances away from the actual fossil and stone tool remains. The Hominin Sites and Paleolakes Drilling Project (HSPDP) was developed to address these issues. The project has focused its efforts on the eastern African Rift Valley, where much of the evidence for early hominins has been recovered. We have collected about 2 km of sediment drill core from six basins in Kenya and Ethiopia, in lake deposits immediately adjacent to important fossil hominin and archaeological sites. Collectively these cores cover in time many of the key transitions and critical intervals in human evolutionary history over the last 4 Ma, such as the earliest stone tools, the origin of our own genus Homo, and the earliest anatomically modern Homo sapiens . Here we document the initial ﬁeld, physical property, and core description results of the 2012–2014 HSPDP coring campaign.


Introduction
The possibility that human evolution has been strongly influenced by changes in the Earth's environmental history, and in particular, its climate history, has been at the forefront of paleoanthropological research for the last 25 years. Few subjects captivate the public interest as much as human evolution and climate change. Today there are compelling scientific and societal needs to clarify the role of climate history in the evolution of our own species, Homo sapiens, and the evolution and extinction of our close relatives (collectively referred to as hominins). Much of the debate about human origins, from the time of the split between the hominins and the ancestors of the African great apes, about 6 Ma, has centered around the fossil record of Africa. This is where the vast majority of hominin fossils > 1 Ma in age have been discovered, and where many important evolutionary transitions in our lineage apparently occurred, such as bipedalism, the use and increasing complexity of stone tools, and increased brain size. Within the African continent, the eastern Rift Valley has been a particularly prominent region for understand-ing human origins, as its deep tectonic basins have provided a depositional context for the accumulation of fossil hominins and other organisms, as well as a sedimentary record allowing us to both date the fossils and put them in a paleoenvironmental context.
Numerous hypotheses linking both global and regional African climate to hominin evolutionary history have been proposed. Vrba (1985Vrba ( , 1988Vrba ( , 1995 hypothesized that Neogene mammalian (including hominin) evolution and extinction occurred in coordinated and relatively rapid turnover pulses triggered by major, directional, global environmental changes, such as the intensification of Northern Hemisphere glaciation. However, mammalian records indicate that the impact of these global mechanisms varied at local and regional levels (Alemseged, 2003;Bobe and Behrensmeyer, 2004;Bobe et al., 2007;Reed, 2008). Other major advances in understanding eastern African paleoclimate (e.g., deMenocal, 1995(e.g., deMenocal, , 2004Trauth et al., 2005;Scholz et al., 2007Scholz et al., , 2011 have spurred the development of explanatory, dynamic paleoclimate models, as well as alternative models linking paleoclimate and human evolution. Potts (1996;Sci. Dril., 21, 1-16, 2016 www.sci-dril.net/21/1/2016/ Potts and Faith, 2015) proposed that it is the variability in climate (especially at orbital forcing timescales) as opposed to simply its directional history (e.g., drying trends) that has driven large-scale evolutionary changes and technological innovations among the hominins. Unfortunately, because local outcrop paleorecords are either incomplete or discontinuous, no consensus yet exists on the factors that interacted to control African climate and ecosystem dynamics during the Plio-Pleistocene or how they affected hominin or other mammalian evolution. On long timescales (> 10 6 years), there is debate on the timing and importance of eastern African uplift and changes in oceanic circulation as causes of climate change, and especially increasing aridity, the development of extensive grassland savanna, and their influence on the mammalian fauna (Cane and Molnar, 2001;Molnar and Cane, 2007;Sepulchre et al., 2006;Wichura et al., 2010;Cerling et al., 2011;Federov et al., 2013;Maslin et al., 2014). On intermediate timescales (10 4 -10 6 years), there is controversy regarding the relative importance of high-latitude glacial cycles, Walker circulation intensification, and annual-to decadalscale variability in atmospheric pressure and sea surface temperatures such as El Niño-Southern Oscillation and the Indian Ocean Dipole (ENSO/IOD) for regional aridity, lake expansions, and seasonality (deMenocal, 2004;Trauth et al., 2009), all of which could have influenced the course of evolution in the lake-rich Rift Valley. On Milankovitch (∼ 100, 40, and 20 kyr) and shorter (10 1 -10 4 years) timescales, there is debate about the role of orbital forcing and high-latitude glacial to millennial-scale events in driving wet-dry cycles that increased environmental pressures on African ecosystems (e.g., Larasoaña et al., 2003;Kingston et al., 2007;Scholz et al., 2007;Campisano and Feibel, 2007;Armitage et al., 2011;Blome et al., 2012), and how these might have influenced resource acquisition (Reed and Rector, 2007) and other ecological parameters affecting hominins. Assessing these hypotheses is complicated by the need to understand the role of biotic drivers of adaptation, such as competition and predation. One fundamental question is whether any of the Earth system drivers can be characterized with sufficient precision to identify drivers of diversification and extinction among our close relatives and ancestors and to enable correlation with hominin evolution.
Past attempts to test hypotheses that implicate climate as a major driver of human evolution have often foundered on a fundamental mismatch of spatial and temporal scales, casting highly temporally resolved, but globally or continentally spatially averaged records of climate change against less temporally resolved but basin-scale records of faunal change and/or hominin evolution. This approach cannot yield a realistic understanding of potential linkages between environmental and biotic change, because it ignores basin-scale environmental dynamics relating to changes in regional climate, that is, local tectonics and geomorphology, which could also be drivers of mammalian population dynamics. For example, Behrens-meyer et al. (1997) tested Vrba's turnover pulse hypothesis by investigating whether such a pulse occurred in changing mammal communities at 2.8 Ma in the Turkana Basin of northern Kenya, a region with a rich and highly continuous fossil record. They found that species patterns in the Turkana Basin did not follow this global model, and that species turnovers were more prolonged responses to climate change associated with both drier and more variable climatic conditions. Tectonic forcing (Bailey et al., 2011) and extreme environmental perturbations, such as megadroughts Scholz et al., 2007), have also been suggested as potential drivers of early modern human population fragmentation, genetic differentiation, range expansion events, and adaptation (Mellars, 2006). The implications of millennial-scale or even shorter events for early hominin evolution have scarcely been explored as they are poorly resolved in offshore marine records. However, such events were clearly linked to major demographic and population-level changes during the Holocene in Africa (e.g., Kuper and Kröpelin, 2006). Current hypotheses remain difficult to test and there has been an acute need to develop new perspectives and data on the links between global-and basin-scale environmental change, and to relate these specific changes to ecological factors that influenced hominin evolution. The Hominin Sites and Paleolakes Drilling Project (HSPDP) was designed to improve understanding of the implications of ecosystem change for hominins in two ways: (1) to provide millennialscale environmental data at key time periods that correspond to morphological and cultural changes or other perceptible evolutionary events in hominin and other mammalian lineages near locations where hominin fossils have been found, and (2) to compare these data across basins, encompassing multiple paleoanthropological localities, to document local versus regional effects of ecosystem change, and responses to global-scale changes. For the specific case of hominin and large mammal evolution in Africa, in order for a paleoenvironmental record to be useful for improving our understanding of the connection between evolution and climate, it must meet two conditions. 1. There must be a highly resolved paleorecord to examine environmental change at any temporal scale that could realistically serve as an evolutionary or ecological trigger. This would range from annual records of seasonality preserved in archives such as annual lake deposits, pollen records of plants responsive to variable seasonality, lipid markers of temperature, etc. to geochemical or sedimentological records of phenomena such as major uplift or paleoceanographic events, which might operate on much longer (e.g., > 10 6 years) timescales.
2. A record of faunal change from the same localities that is sufficiently detailed to investigate responses to environmental change within particular clades, ecological guilds, or mammal communities.
www.sci-dril.net/21/1/2016/ Sci. Dril., 21, 1-16, 2016 The HSPDP was developed by an international team of over 100 scientists from 11 countries to address these issues. Its goal was the collection and analysis of high-resolution paleoenvironmental records from paleo-lake drill cores near the depocenters of lacustrine basins of significant paleoanthropological importance in eastern Africa, each of which meets these conditions. As discontinuously exposed outcrops have shown these lakebeds to be commonly laminated (e.g., Wilson et al., 2014) with bedding characteristics often similar to demonstrably annual varves documented in modern African rift lakes (Pilskaln and Johnson, 1991;Cohen et al., 2006) and deposited at high sedimentation rates, their records fulfill the first criterion. The second criterion is fulfilled as each of the drill sites lies in close proximity to rich and diverse fossil vertebrate and archaeological sites, with sediments of the same age, and which collectively span some of the most critical intervals of hominin evolutionary history (e.g., earliest Homo, earliest stone tools, origin of Acheulian and Middle Stone Age technologies, earliest modern H. sapiens), and where new, important fossils and artifacts are still being recovered. Thus, the integration and direct comparison of basin-scale records of environmental change from cores with the record of faunal and cultural change from outcrops affords us the opportunity to test existing hypotheses of Earth system drivers of evolution at different temporal and spatial scales.

Drilling target areas
A series of workshops held in the mid-late 2000s better defined the specific goals of the HSPDP and specific selection criteria for ideal drilling locations . The drilling areas (Table 1 and Fig. 1) were decided through a lengthy and interactive process between the principal ICDP project proponents. Numerous hominin fossil and archaeological sites in proximity to lake deposits in eastern Africa were considered as potential drilling targets, and ultimately the decision on which sites to pursue was determined by a combination of the scientific criteria mentioned above, along with practical, logistical considerations, such as site access for a truck-mounted drill rig and probable costs. The sites discussed below were part of the original HSPDP operational plan. The Olorgesailie (Koora Plain) site was ultimately funded separately from the remaining ICDP-supported sites.

The Northern Awash drilling area, Ethiopia
The Northern Awash basin provides one of the densest accumulations of early hominin fossils (Johanson et al., 1982;Kimbel et al., 2004;Alemseged et al., 2006), as well as rich mammalian faunal and floral records (Bonnefille et al., 2004;Reed, 2008;Geraads et al., 2012). Its lakebeds provide a potential record of the local environmental response to the onset of high-amplitude climate oscillations and increased aridity in eastern Africa at ∼ 3.15 Ma as well as the response to Milankovitch cycles prior to the onset of high-latitude glaciation (∼ 2.7 Ma) as documented in the marine core record (Campisano and Feibel, 2007). This site provides a backdrop against which ∼ 400 kyr of the evolutionary history of Australopithecus afarensis (e.g., "Lucy") and associated fauna and the earliest use of stone tools (McPherron et al., 2010) will be interpreted.

The Baringo Basin/Tugen Hills drilling area, Kenya
This area of the central Kenyan Rift Valley comprises the most complete late Neogene section known from the African rift (Chapman and Brook, 1978). The stratigraphic interval of the Chemeron Formation targeted here (3.3-2.6 Ma) contains ∼ 100 fossil vertebrate localities, including three hominin sites, providing an opportunity to explore the nature of environmental change associated with shifting insolation patterns (for example, documenting the lacustrine response to changing precipitation patterns at precessional, millennial, and perhaps even shorter timescales; e.g., Kingston et al., 2007;Wilson et al., 2014) and to assess specific terrestrial community responses to pervasive, short-term climatic change through the interval of Northern Hemisphere glacial intensification. At this time in eastern Africa we also observe the diversification of Paranthropus (a group of hominins with robust cranial features and large teeth for a strong bite force) and our own genus Homo, as well as the earliest evidence for stone tool-making in nearby West Turkana (Harmand et al., 2015).

The West Turkana drilling area, Kenya
This area targets the Early Pleistocene lakebeds of Turkana, Kenya, that were deposited during a phase of overall increasing continental aridity punctuated by major lake-level fluctuations, which appear to reflect insolation-forced climate cycles (Lepre et al., 2007;Joordens et al., 2011). The extensive outcrops of the Turkana Basin have been well character-ized geologically (Feibel, 2011) and have provided an unparalleled tephrostratigraphic framework (Brown et al., 2006) associated with precise chronostratigraphic controls (Mc-Dougall et al., 2012). This borehole is in direct proximity to the rich fossil record of the Turkana Basin, including ∼ 500 hominin fossils and more than 100 archaeological sites (Harris et al., 1988;Roche et al., 2004). The hominins include significant specimens, such as the earliest/most complete specimens of H. rudolfensis and H. erectus, early members of our own genus. The time window targeted here (∼ 1.9-1.4 Ma) also includes the earliest evidence of Acheulean (e.g., large hand axes) stone tool technology (Lepre et al., 2011)  These drill sites comprise contemporaneous Early Pleistocene to modern records from two adjacent (but hydrologically distinct) basins. Drill cores from these localities in the southern Kenya rift may provide a regional equatorial paleoclimate history of the major Middle-Late Pleistocene climate transitions, which is otherwise recorded from this region in only discontinuous records. Drilling on the Koora Plain will allow us to examine deposits immediately adjacent to the Olorgesailie depositional basin, one of the richest, bestcalibrated Early-Late Pleistocene archeological localities in Africa, with abundant Acheulean and Middle Stone Age (MSA) sites (and documenting the transition between these important technological phases of human prehistory), diverse fauna, a detailed paleoenvironmental record, and abundant tephras (e.g., Potts et al., 1999;Sikes et al., 1999;Behrensmeyer et al., 2002;Owen et al., 2008). Prior research here has fueled hypotheses and debates about climate-evolution relationships (e.g., Owen et al., 2009a, b;Trauth and Maslin, 2009). Nearby Lake Magadi (∼ 20 km from the Koora Plain drill site) is located in the axis of the southern Kenya Rift and is a regional sump for water and sediments. The present lake, a saline/alkaline pan, is the successor to a series of paleolakes that have occupied the basin since the Early Pleistocene. Previous outcrop and drill core records (none of which survive) established the volcanic and sediment stratigraphy and their linkage to basin hydrology (Baker, 1958;Surdam and Eugster, 1976;Crossley, 1979;Eugster, 1980;Jones et al., 1977). The close proximity of both basins will provide us with an opportunity to tease out climatic from tectonic/groundwater controls on their respective environmental histories, contributing to HSPDP Objective 2 -the evaluation of how global climate changes were experienced locally within key hominin locales.

The Chew Bahir drilling area, Ethiopia
This area comprises Middle-Late Pleistocene lakebeds in a region between the Ethiopian and Omo-Turkana rifts, each of which has a highly distinctive Quaternary biogeographic history (Suwa et al., 2003) and border presumed habitat refuge areas during times of climatic stress . Chew Bahir is an ephemeral playa today, but in the past has held a large lake (Foerster et al., 2012). Our records from Chew Bahir, presumed to cover at least the last 700 kyr, will also provide a regional-scale environmental context for the earliest anatomically modern H. sapiens fossils recovered at ∼ 200 ka in the nearby (90 km away) Omo River valley (Day, 1969;McDougall et al., 2005;Brown et al., 2006). When coupled with the other Early Pleistocene-recent HSPDP records from Olorgesailie and Magadi and previously collected drill core records from Lake Malawi and elsewhere in the region, the details of regional environmental heterogeneity in eastern Africa through the extreme climatic fluctuations of the Quaternary may be explored (e.g., Blome et al., 2012).

Pre-drilling site surveys
Between 2008 and 2012 subsurface and outcrop site survey data were collected in a series of campaigns from all of the drill sites to determine optimal locations for the various boreholes. The objective was to minimize the likelihood of encountering subsurface faults or associated deformation and to maximize stratigraphic resolution. Seismic data were acquired by our group at the Afar, West Turkana and Olorgesailie areas. Additionally, legacy industry seismic data were obtained from an old (1970s) AMOCO survey at West Turkana and very recently acquired survey data from Tullow Oil at the Chew Bahir area. Gravity and magnetic surveys were also conducted by our team at the Magadi and Olorgesailie areas. Prior boreholes drilled by the US Geological Survey in the late 1960s at Lake Magadi provided additional information for that area. Siting at the Baringo Basin/Tugen Hills was based on known outcrop exposures immediately adjacent to the drill site.

Drilling and logging operations (Figs. 2 and 3)
Drilling of the HSPDP sites took place over an approximately 2-year period between September 2012 and December 2014. Local drilling contractors, Drilling and Prospecting International for Kenya areas, Addis GeoSystems for the Chew Bahir pilot hole, and Geosearch (now Orezone Drilling) for all other holes in Ethiopia, provided truck-mounted standard wireline diamond coring drill rigs and crews. DOSECC Exploration Services (DES) provided drilling operations oversight, local supervision and specialized lake tools, bits, and other drilling supply procurement for items that were not locally available. Boreholes were drilled using a combination of H (96.3 mm diameter hole, 61.1 mm diameter core), P (122.6 mm hole, 66 mm core), and minor N (75.7 mm hole, 47.6 mm core, at Awash) diameter drill string and a variety of coring tools depending on the highly variable lithologic conditions encountered during drilling. P was employed when using the specialized lake coring tools in unconsolidated sediments. These included the hydraulic piston corer, the "extended nose" non-rotating corer, "alien" rotating corer, all using standard IODP butyrate core liners. Boreholes were  After drilling each site, cores were shipped via airfreight to LacCore, the National Lacustrine Core Facility (University of Minnesota) for full scanning, processing, description, and subsampling. Physical properties for cores from all sites were analyzed in detail via MSCL-S (whole core, for p wave velocity, gamma density, loop MS, non-contact electrical resis- tivity, natural gamma radiation) and MSCL-XYZ (split core, for high-resolution MS and color reflectance spectrophotometry) at increments ranging from 0.5 to 4 cm, depending on the parameter. Cores were split in half lengthwise, cleaned, and scanned with a Geotek © MSCL-CIS digital linescan core imager. Visual core description, smear slide analysis, and (as needed) SEM-EDS and XRD analyses were performed, and subsamples were extracted according to coordinated plans for stratigraphically equivalent samples for all analytical parameters.

Initial coring and core description results
In total, 18 boreholes were drilled in the HSPDP (Table 1), although several of these were "deadman" anchoring holes to secure the drill rig and not intended for core recovery. Approximately 2 km of core was recovered from about 2200 m of cored intervals, for an average recovery of ∼ 90.5 %. The only area where recovery was significantly below this average was at the Lake Magadi site, where interbedded hard and soft lithologies (cherts and unconsolidated muds) made for extremely challenging coring conditions. Six boreholes were drilled at the Northern Awash area from two sites (NAO/Osi Isi and NAW/Woranso, Fig. 2a Key to all lithologic symbols Figure 4. Key to all lithologic symbols. Note that blank (white) areas in lithologic columns indicate zones of missing core, i.e., no core recovery. graphic interval covered by the two sites to be approximately 270 m. Boreholes consisted of three primary science boreholes inclined 13-15 • , plus two cored anchoring holes and one uncored hole, all of which were drilled in February-March 2014. Thick basalt sections were encountered at both sites (some of which appear to be compound flows), which are separated by about 3 km. Sediments at both drill sites are gently dipping (∼ 2 • NE). The two longest cores (NAO-1B, Fig. 5 and NAW-1A, Fig. 6) consist of primarily massive or laminated, brown or greenish brown silty clays, with occasional sandy units scattered through the core, particularly associated with the upper basalt (Fig. 7a, b). Diatomites occur sporadically, mostly in the upper portions of both cores, with diatomaceous units more abundant below the second basalt. Thin (mm-cm) unaltered airfall volcanic ashes occur throughout the core. Most of the pronounced low-MS and low gamma density zones consist of either diatomites or fine, greenish clays. The brown clays contain abundant paleosol nodules and occasional beds of gastropods. Drilling at both the NAO and NAW localities was terminated when advancing the holes became impractical as rods became stuck  because of very tight hole conditions, very high torque, and water pressure. A single, vertical ∼ 228 m borehole was drilled at the Tugen Hills site in May-June 2013 (Fig. 8). The borehole was situated in very close proximity to exposures of variably dipping (20-42 • in the borehole) cyclic diatomites and mudstones of the upper Chemeron Formation, which had previously been shown by Deino et al. (2006) and Kingston et al. (2007) to reflect extreme precessional climate variability in the central Kenyan Rift during the Plio-Pleistocene transition. The lower ∼ 100 m of the core is coarser on average than the upper part of the core. From the base to ∼ 130 m b.s. the core contains frequent channelized granular sands and conglomerate beds (often reddish in color), alternating with carbonate nodular paleosol siltstones (Fig. 7c) lacustrine muds and diatomites. Above this, diatomite lacustrine/terrestrial cycles similar to those seen in outcrop begin to appear (evident in both the lithologies and physical properties of the upper portion of the drill core, Fig. 7d). Lowdensity, low-magnetic-susceptibility sediments (light colored lacustrine diatomites and clays) alternate with more strongly magnetically susceptible and denser siliciclastic muds (paleosols, often with abundant carbonate nodules) and fluvial sands (and occasional gravels) in the upper 130 m of the core. Sediments above ∼ 50 m b.s. are generally lighter in color (note grey-scale data, Fig. 8), which may reflect near-surface weathering/alteration above the local water table. Numerous primary and reworked tephras occur throughout the core, which will be critical for dating the core. Drilling was terminated at this site close to the original planned target depth (250 m) for budgetary reasons. A single, oriented (10 • from vertical) ∼ 216 m borehole was drilled at the West Turkana (WTK) site in June-July 2013 (Figs. 2c, d and 9). The drill site was chosen to be in close proximity to outcrop exposures of the correlative Nachukui Formation, which is locally dipping at ∼ 5 • W. The lower ∼ 155 m (61-216 m b.s.) of the core consists of laminated to massive green and brown clays, which are often fossiliferous (fish, ostracodes and molluscs, the latter often organized as discrete shell lags) (Fig. 7e). Many of these lacustrine clays contain paleosol structure and carbonate nod-ules indicative of episodic exposure and pedogenesis. Above 61 m b.s., a pronounced lithologic transition occurs towards coarser sediments (more frequent sandy intervals), which is also reflected in changes in the color and magnetic susceptibility of the core. Soil structure and nodular carbonates occur in these sediments as well. Tuffs occur as discrete horizons at several depths within the core, which at this locality will be critical for tephrostratigraphic correlation with nearby outcrops. Drilling was terminated at this site when borehole instability, high torque, and high-pressure groundwater caused an inability for the drilling to advance. Bottom hole temperatures also began to rise abruptly near the base of the hole, indicating a potential hydrothermal hazard.
Three vertical boreholes were drilled (and two cored) at the northern end of the Koora Plain, in the southern Kenya Rift Valley, ∼ 22 km SSW of the Olorgesailie archaeological site in September-October 2012 (Figs. 2d, 10, and 11). Because the DOSECC soft sediment tools were not available at this time, the upper, unconsolidated sediments of both boreholes were auger drilled and cuttings were bagged at Site 1. Excellent core recovery was achieved at both sites below the augered intervals (Table 1 and Figs. 10 and 11). Both cores consist of flat-lying, interbedded muds (laminated in part), diatomites, and fine to coarse sands, with some pumice-rich gravel and conglomerate intervals and infrequent carbonate marls as well. Numerous tuffs are also present. Both cores bottomed in the trachyte basement that underlies the basin at depths of ∼ 166 and 116 m for Sites 1 and 3, respectively.
Four vertical boreholes at two sites were drilled into flatlying sediments at Lake Magadi in June 2014, and downhole logs were made in the single borehole at Site 2 (Figs. 3a, 12, 13). Unlike other sites, it was necessary to drill from a raised pad at Lake Magadi, because the surface trona crust was inundated and soft from recent rains. A custom-built pad was constructed by the project for Site 1 adjacent to the main causeway crossing the lake, whereas Site 2 took advantage of a wide area along another existing elevated roadbed on the playa. Also in contrast to the other drilling targets, the Lake Magadi sediments consist of large proportions of trona (Fig. 7f) and other Na carbonates and chert (Fig. 7g, as well as both laminated (Fig. 7h) and massive lacustrine muds. Muds, mudstones, and cherts in varying proportions dominate the lower stratigraphic intervals at both sites, whereas the upper portion at both sites is a 30-40 m thick sequence of trona and trona-bearing muds, the production target for Tata Chemicals, our local industry partner for this drill site. The upper trona was drilled using freshwater as the drilling fluid in the initial holes because bentonite drilling mud would not mix with the high-pH brines readily available near the site. However, this strategy proved problematic because dissolution cavities formed around the borehole, undermining site stability. For boreholes 1C and 2A drilling used only the high-pH lake brine without bentonite, which ultimately proved satisfactory because the high density of the brine was sufficient to raise the cuttings. The alternation of soft and www.sci-dril.net/21/1/2016/ Sci. Dril., 21, 1-16, 2016 lithified muds and cherts (often on a sub-meter depth scale) proved a challenging coring environment. Percent core recovery at this site (in the 45-65 % range) was consequently below the levels achieved at other sites. Drilling at both locations was terminated when the boreholes reached the trachytic basement rocks (at depths of ∼ 136 and 197 m for Sites 1 and 2, respectively). An exploratory shallow coring campaign was conducted at the Chew Bahir area in 2009 and 2010 along a NW-SE transect from the basin margin to the center, which recovered six short sediment cores of 9-18.8 m length (Foerster et al., 2012Trauth et al., 2015). Subsequently, a pilot drilling operation was conducted in the center of the Chew Bahir basin in March 2014 (∼ 41 m vertical borehole). Drilling at this site was terminated when flooding made the drilling site inaccessible. This was followed by the drilling of two considerably deeper, twinned vertical boreholes (∼ 279 and 266 m in flat-lying sediments for boreholes 2A and 2B, respectively, Figs. 14, 3b) in a slightly more proximal and elevated position relative to the basin margin in November-December 2014. The CHB14-2A and 2B cores consist predominantly of reddish, brown or green silty and sandy clays, with occasional silt and calcareous sand beds. Discrete shellrich and plant debris-rich horizons occur throughout the cores. Carbonate nodule-rich muds are more common in the lower part of the core (below ∼ 90 m b.s.). Drilling was terminated when advancing became impractical and funds were depleted.

HSPDP outreach and education activities
The HSPDP has made a priority of developing an effective outreach and educational program that makes the project's goals and findings accessible to the broader public. Prior to and during drilling activities at each study area, an intensive effort was made to engage with the local public about our activities. This often involved having Kenyan and Ethiopian research and museum outreach specialists make presentations using visual aids such as segments of sediment cores or casts of hominin skulls to explain the science objectives and (importantly) to dispel misunderstandings concerning the nature of our drilling activities (which were commonly assumed to be for resource exploration prior to these presentations) (Fig. 3c). The HSPDP has also worked closely with the National Museums of Kenya and Ethiopia, as well as several museum institutional partners in the US, in the development of post-drilling educational resources that these museums can use in the future to explain the intersection between human evolutionary history and climate history. The most visible of these efforts has the been the development of a short (14 min) 3-D film, produced by the nonprofit Earth Images Foundation (www.earthimage.org), and funded jointly by the US National Science Foundation and ICDP, which documents both the important science questions underpinning the HSPDP as well as the excitement associated with the drilling and core analysis activities (Fig. 3d). This film will be on long-term display in the human origins halls at the partner museums, and is also available in 2-D format via the project website (http://hspdp.asu.edu) and Facebook page (www.facebook.com/HSPDP). The HSPDP has a strong social media presence through its Facebook site and project website, where educational resources, such as numerous photographs of drilling and initial core description activities are made available to the general public. Another exciting and innovative HSPDP outreach activity has been the involvement of an "artist in residence", funded through our UK NERC grant. The artist, Julian Ruddock, will be using highresolution photographs and video footage including interviews he has conducted during drilling activities at the Chew Bahir site, as well as core images to create an art/science collaboration for gallery display in the UK starting in 2016 http://cargocollective.com/artscienceclimatechange/ Earth-Core-The-Hominin-Project. HSPDP members, led by co-PI Martin Trauth, are currently teaching a series of sum- mer schools in the bio-geosciences that help twenty young scientists from African and European universities to design new research projects on these topics, using the latest methods of data analysis, and to present the results from these projects in an attractive and professional manner. The overall topic of the summer school, held in Ethiopia (September-October 2015) and Kenya (February-March 2016), is tectonics, climate, and human evolution, using the latest results from the HSPDP as the basis of discussions during the event.

Future plans
Now that all HSPDP-related drilling is completed, all cores are being analyzed for a wide variety of geochronological, geochemical, sedimentological and paleoecological studies, to assemble a high-resolution record of environmental change at each of the study sites. The geochronology of the cores is being assembled through a combination of highprecision Ar/Ar, paleomagnetics, U-series, tephrostratigraphy, luminescence and (for the most recent parts of the cores) 14 C dating. State-of-the-art organic geochemical and clumped isotope proxies of paleotemperature and paleoprecipitation are being applied to the cores. The wide array of fossils (diatoms, ostracodes, molluscs, fish, pollen, phytoliths and charcoal) are also being exploited for the information they provide about both lake and watershed paleoecological conditions. Scanning XRF, XRD, and MSCL log records are also providing extremely high-resolution records of paleoenvironmental and provenance history at each site. Another important component of this analysis is the integration of core data with nearby outcrop information about paleoenvironments of hominins and other fossils and stone tools. Extensive interaction between the data collection and modeling teams of the HSPDP is also underway, to ensure that plausible explanations of climate and landscape dynamics are developed and tested against the core and outcrop data. Ultimately, through interaction between the core analysts and paleoanthropologists involved in the HSPDP, we hope to use our new high-resolution core data and climate/landscape models to both re-evaluate existing models linking hominin evolution with climate and propose new ones consistent with the vast new data set assembled by the HSPDP.