Bones of recent mammals in the Amboseli Basin, southern Kenya, exhibit distinctive weathering characteristics that can be related to the time since death and to the local conditions of temperature, humidity and soil chemistry. A categorization of weathering characteristics into six stages, recognizable on descriptive criteria, provides a basis for investigation of weathering rates and processes. The time necessary to achieve each successive weathering stage has been calibrated using known-age carcasses. Most bones decompose beyond recognition in 10 to 15 yr. Bones of animals under 100 kg and juveniles appear to weather more rapidly than bones of large animals or adults. Small-scale rather than widespread environmental factors seem to have greatest influence on weathering characteristics and rates. Bone weathering is potentially valuable as evidence for the period of time represented in recent or fossil bone assemblages, including those on archeological sites, and may also be an important tool in censusing populations of animals in modern ecosystems.

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The Siwalik formations of northern Pakistan consist of deposits of ancient rivers that existed throughout the early Miocene through the late Pliocene. The formations are highly fossiliferous with a diverse array of terrestrial and freshwater vertebrates, which in combination with exceptional lateral exposure and good chronostratigraphic control allows a more detailed and tem porally resolved study of the sediments and faunas than is typical in terrestrial deposits. Conse quently the Siwaliks provide an opportunity to document temporal differences in species richness, turnover, and ecological structure in a terrestrial setting, and to investigate how such differences are related to changes in the fluvial system, vegetation, and climate. Here we focus on the interval between 10.7 and 5.7 Ma, a time of significant local tectonic and global climatic change. It is also the interval with the best temporal calibration of Siwalik faunas and most comprehensive data on species occurrences. A methodological focus of this paper is on controlling sampling biases that confound biological and ecological signals. Such biases include uneven sampling through time, differential preservation of larger animals and more durable skeletal elements, errors in age-dating imposed by uncertainties in correlation and paleomagnetic timescale calibrations, and uneven taxonomic treatment across groups. We attempt to control for them primarily by using a relative-abun dance model to estimate limits for the first and last appearances from the occurrence data. This model also incorporates uncertainties in age estimates. Because of sampling limitations inherent in the terrestrial fossil record, our 100-Kyr temporal resolution may approach the finest possible level of resolution for studies of vertebrate faunal changes over periods of millions of years. Approximately 40,000 specimens from surface and screenwash collections made at 555 localities form the basis of our study. Sixty percent of the localities have maximum and minimum age esti mates differing by 100 Kyr or less, 82% by 200 Kyr or less. The fossils represent 115 mammalian species or lineages of ten orders: Insectivora, Scandentia, Primates, Tubulidentata, Proboscidea, Pholidota, Lagomorpha, Perissodactyla, Artiodactyla, and Rodentia. Important taxa omitted from this study include Carnivora, Elephantoidea, and Rhinocerotidae. Because different collecting methods were used for large and small species, they are treated separately in analyses. Small spe cies include insectivores, tree shrews, rodents, lagomorphs, and small primates. They generally weigh less than 5 kg. The sediments of the study interval were deposited by coexisting fluvial systems, with the larger emergent Nagri system being displaced between 10.1 and 9.0 Ma by an interfan Dhok Pathan sys tem. In comparison to Nagri floodplains, Dhok Pathan floodplains were less well drained, with smaller rivers having more seasonally variable flow and more frequent avulsions. Paleosol se quences indicate reorganization of topography and dra...

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Downloaded fromwhen approaching the HOMO or LUMO resonance of the molecular wire (28). The increased conductance at higher bias voltages then compensates for the molecular wire length increase in Fig. 4B (a factor of 40 is not sufficient for the achieved current increase). Thus, such a setup allows the determination of the small conductance (8.6 × 10 -13 S) of a single and the same molecular wire with 20 nm length (the conductance at small bias voltages cannot be measured over such a large distance, due to the extremely low current-below the detection limit-passing through the polymer in this case). In this regard, it would be interesting to prepare and study conjugated polymers with smaller HOMO-LUMO gaps. Such molecular wires should exhibit higher conductances and allow charge transport to be determined over even larger distances. Hominin footprints offer evidence about gait and foot shape, but their scarcity, combined with an inadequate hominin fossil record, hampers research on the evolution of the human gait. Here, we report hominin footprints in two sedimentary layers dated at 1.51 to 1.53 million years ago (Ma) at Ileret, Kenya, providing the oldest evidence of an essentially modern human-like foot anatomy, with a relatively adducted hallux, medial longitudinal arch, and medial weight transfer before push-off. The size of the Ileret footprints is consistent with stature and body mass estimates for Homo ergaster/erectus, and these prints are also morphologically distinct from the 3.75-millionyear-old footprints at Laetoli, Tanzania. The Ileret prints show that by 1.5 Ma, hominins had evolved an essentially modern human foot function and style of bipedal locomotion. Bipedalism is a key human adaptation that appears in the fossil record by 6 million years ago (Ma) (1). Considerable debate continues over when and in what context a modern human-like form of bipedalism evolved, because of a fragmentary record and disagreements over the functional interpretations of existing fossils and footprints (2-7). Modern human footprints reflect the specialized anatomy and function of the human foot, which is characterized by a fully adducted hallux, a large and robust calcaneus and tarsal region, a pronounced medial longitudinal arch, and short toes (2). Footprints reflect the pressure distribution as the foot makes contact with the substrate, but also the sediment's geomechanical properties (8). During normal walking, the weight-bearing foot undergoes a highly stereotypical movement and pressure distribution pattern in which the heel contacts the ground first, making a relatively deep impression on the substrate. This is followed by contact with the lateral side of the foot and metatarsal heads, after which weight transfers to the ball of the foot with peak pressure under the medial metatarsal heads, and finally ending with toe-off pressure under the hallux (9, 10). As a consequence, the deepest part of a footprint often occurs beneath the first and second metatarsal heads, that along with a deep hallucal impression cor...

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