Paleobiology of the oligopithecines,the earliest known anthropoid primates

Anthropoid primates of the subfamily Oligopithecinae are late Eocene in age, and have a known distribution of Northeast Africa and the Arabian Peninsula. Body sizes of the three known oligopithecine species are estimated from allometric molar size regressions to be 700–1000 g forOligopithecus savagei, 600–900 g forCatopithecus browni, and 500 g for the least well-known and smallest species,Proteopithecus sylviae. Occlusal features of the molar teeth, considered in conjunction with body size, suggest that all three species were frugivorous and insectivorous. The orbital size ofCatopithecus indicates a diurnal activity cycle. A relatively broad interobital region in this species may indicate prosimian-like or callitrichid-like olfactory adaptations. Structural features of the crushed skull suggest thatCatopithecus had a smaller cranial capacity than those of extant anthropoids with a similar body size. Fossil plants and birds from localities yielding oligopithecines suggest a wet, warm, tropical, forested, swampy environment. These paleobiological inferences about the extinct oligopithecines are discussed in relation to questions about primate adaptations near the prosimian-anthropoid transition.     

How did bonobos come to range south of the congo river? Reconsideration of the divergence of Pan paniscus from other Pan populations

While investigating the genetic structure in wild bonobos,¹ we realized that the widely accepted scenario positing that the Pleistocene appearance of the Congo River separated the common ancestor of chimpanzees (Pan troglodytes) and bonobos (P. paniscus) into two species is not supported by recent geographical knowledge about the formation of the Congo River. We explored the origin of bonobos using a broader biogeographical perspective by examining local faunas in the central African region. The submarine Congo River sediments and paleotopography of central Africa show that the Congo River has functioned as a geographical barrier for the last 34 million years. This evidence allows us to hypothesize that when the river was first formed, the ancestor of bonobos did not inhabit the current range of the species on the left bank of the Congo River but that, during rare times when the Congo River discharge decreased during the Pleistocene, one or more founder populations of ancestral Pan paniscus crossed the river to its left bank. The proposed scenario for formation of the Congo River and the corridor hypothesis for an ancestral bonobo population is key to understanding the distribution of great apes and their evolution.     

盘县大洞古人类遗址的地层和古气候研究

贵州盘县大洞的堆积物,自上而下可以分为3层。大洞主体堆积物为角砾堆积,来源于洞顶灰岩的崩塌,另外有人类遗物以及洞外片流作用带入的泥砂。人类化石、旧石器和哺乳动物化石主要分布在第2层角砾堆积中。堆积物在洞厅各部位均有相应分布,属同一沉积序列。已知的早期人类活动时间大约从260ka．B．P．开始,到142ka．B．P．前后结束,对应于深海氧同位素的第6、7阶段。角砾层下段,发育一套遭强烈溶蚀和风化的堆积物,地球化学分析结果显示其湿热的沉积环境,时间大约在260—180ka B．P．期间,对应于深海氧同位素第7阶段;大洞堆积物在气候变化周期上与黄土、青藏高原冰期序列可以对比。     

古菌和细菌四醚膜脂GDGTs的生物合成机制及其生物地球化学意义

以甘油二烷基甘油四醚(glycerol dialkyl glycerol tetraethers,GDGTs)为主的跨膜醚脂化合物是古菌和部分细菌细胞膜的重要组成成分。作为分子化石,GDGTs化合物对环境变化响应敏感,以其为基础的有机地球化学指标在定量重建海洋与陆地的古环境研究中发挥出独特的优势。然而,GDGTs指标在广泛应用的同时也不断出现适用性和准确性问题。其关键原因在于GDGTs的生物合成和生理机制研究相对匮乏,难以为指标提供分子生物学与生理学基础。近年来,在多学科的交叉融合下,古菌类异戊二烯GDGTs的生物合成研究取得了令人瞩目的进展。这些成果为脂类生物标志物的地学应用及生物源的确定提供了可靠的生物学基础和新的研究思路。本文综述了古菌类异戊二烯GDGTs的生物合成过程,提出了细菌支链GDGTs生物合成途径的假说,讨论了GDGTs生理过程的生物地球化学意义,并初步展望了GDGTs研究领域未来重要的发展方向。     

Multiple stages of plant root calcification deciphered by chemical and micromorphological analyses

Rhizoliths, that is, roots fossilized by secondary carbonates, have been known for ages and are increasingly used for paleoenvironmental reconstructions. However, knowledge about their formation mechanisms remains limited. This study reports the mineralogical and chemical characterization of rhizoliths at different stages of mineralization and fossilization in the Late Pleistocene loess–paleosol sequence of Nussloch (SW Germany). Scanning electron microscopy coupled with elemental mapping and ¹³C solid‐state nuclear magnetic resonance were used to concomitantly characterize the mineral and organic matter of the rhizoliths. These joint analyses showed for the first time that large rhizoliths are not necessarily remains of single large roots but consist of numerous microrhizoliths as remains of fine roots, formed mainly by calcium carbonates with only low amounts of Mg and Si. They further revealed that the precipitation of secondary carbonates occurs not only around, but also within the plant root and that fossilization leads to the selective preservation of recalcitrant root biopolymers—lignin and suberin. The precipitation of secondary carbonates was observed to occur first around fine roots, the epidermis acting as a first barrier, and then within the root, within the cortex cells, and even sometimes around the phloem and within the xylem. This study suggests that the calcification of plant roots starts during the lifetime of the plant and continues after its death. This has to be systematically investigated to understand the stratigraphic context before using (micro)rhizoliths for paleoenvironmental reconstructions in terrestrial sediments.     

The late‐stage “ferruginization” of the Ediacara Member (Rawnsley Quartzite,South Australia): Insights from uranium isotopes

The paleoenvironmental setting in which the Ediacara Biota lived, died, and was preserved in the eponymous Ediacara Member of the Rawnsley Quartzite of South Australia is an issue of long‐standing interest and recent debate. Over the past few decades, interpretations have ranged from deep marine to shallow marine to terrestrial. One of the key features invoked by adherents of the terrestrial paleoenvironment hypothesis is the presence of iron oxide coatings, inferred to represent the upper horizons of paleosols, along fossiliferous sandstone beds of the Ediacara Member. We find that these surficial oxides are characterized by (²³⁴U/²³⁸U) values which are not in secular equilibrium, indicating extensive fluid‐rich alteration of these surfaces within the past approximately 2 million years. Specifically, the oxide coatings are characterized by (²³⁴U/²³⁸U) values >1, indicating interaction with high‐(²³⁴U/²³⁸U) fluids derived from alpha‐recoil discharge. These oxides are also characterized by light “stable” δ^238/235U values, consistent with a groundwater U source. These U isotope data thus corroborate sedimentological observations that ferric oxides along fossiliferous surfaces of the Ediacara Member consist of surficial, non‐bedform‐parallel staining, and sharply irregular patches, strongly reflecting post‐depositional, late‐stage processes. Therefore, both sedimentological and geochemical evidence indicate that Ediacara iron oxides do not reflect synsedimentary ferruginization and that the presence of iron oxides cannot be used to either invoke a terrestrial paleoenvironmental setting for or reconstruct the taphonomic pathways responsible for preservation of the Ediacara Biota. These findings demonstrate that careful assessment of paleoenvironmental parameters is essential to the reconstruction of the habitat of the Ediacara Biota and the factors that led to the fossilization of these early complex ecosystems.     

Paleosols and paleoenvironments of the middle Miocene,Maboko Formation,Kenya

The middle Miocene (15 Ma) Maboko Formation of Maboko Island and Majiwa Bluffs, southwestern Kenya, has yielded abundant fossils of the earliest known cercopithecoid monkey (Victoriapithecus macinnesi), and of a kenyapithecine hominoid (Kenyapithecus africanus), as well as rare proconsuline (Simiolus leakeyorum, cf. Limnopithecus evansi) and oreopithecine apes (Mabokopithecus clarki, M. pickfordi), and galagids (Komba winamensis). Specific habitat preferences can be interpreted from large collections of primate fossils in different kinds of paleosols (pedotypes). Fossiliferous drab-colored paleosols with iron-manganese nodules (Yom pedotype) are like modern soils of seasonally waterlogged depressions (dambo). Their crumb structure and abundant fine root-traces, as well as scattered large calcareous rhizoconcretions indicate former vegetation of seasonally wet, wooded grassland. Other fossiliferous paleosols are evidence of nyika bushland (Ratong), and early-successional riparian woodland (Dhero). No fossils were found in Mogo paleosols interpreted as saline scrub soils. Very shallow calcic horizons (in Yom, Ratong, and Mogo paleosols) and Na-montmorillonite (in Mogo) are evidence of dry paleoclimate (300-500 mm MAP=mean annual precipitation). This is the driest paleoclimate and most open vegetation yet inferred as a habitat for any Kenyan Miocene apes or monkeys. Victoriapithecus was abundant in dambo wooded grassland (Yom) and riparian woodland (Dhero), a distribution like that of modern vervet monkeys. Kenyapithecus ranged through all these paleosols, but was the most common primate in nyika bushland paleosols (Ratong), comparable to baboons and macaques today. Mabokopithecus was virtually restricted to riparian woodland paleosols (Dhero), and Simiolus had a similar, but marginally wider, distribution. Habitat preferences of Mabokopithecus and Simiolus were like those of modern colobus monkeys and mangabeys. A single specimen of Komba was found in dambo wooded grassland paleosol (Yom), a habitat more like that of the living Senegal bushbaby than of rainforest galagids. A shift to non-forest habitats may explain the terrestrial adaptations of Victoriapithecus, basal to the cercopithecid radiation, and of Kenyapithecus, basal to the hominoid radiation. Both taxa are distinct from earlier Miocene arboreal proconsulines, oreopithecines and galagids.     

Studies in Neotropical paleobotany. XI. Late Tertiaryvegetation and environments of southeastern Guatemala: palynofloras fromthe Mio-Pliocene Padre Miguel Group and the Pliocene HerreriaFormation

Plant microfossils are reported from the late Tertiary Padre MiguelGroup and the Pliocene Herrería Formation of southeasternGuatemala. The most abundant palynomorphs are cf. Acrostichum(maximum 45%), Cyperaceae (29%), cf. Antrophyum(27%), monolete fern spores (16%), and Pinus(11%). Pollen grains of Picea, Juglans,Quercus, and Ulmus, primarily from the Padre Miguelflora, reveal the presence of a northern cool-temperate element. Theyounger Herrería flora is more lowland and warm temperate. Inthe absence of evidence for substantially higher elevations, thedifferences between the Neogene and modern vegetation are attributedmostly to climate. MAT (mean annual temperature) is estimated2°-3°C cooler than at present for the Padre Miguel flora,and ～3.5°C warmer for the Herrería flora. There islittle evidence for arid vegetation, and the tropical rain forest wasabsent or poorly represented. These data are consistent with those ofother fossil floras in the region and with trends suggested by isotopicpaleotemperature analysis and global sea-level changes. The Guatemalaassemblages further provide evidence that the current version of thetropical rain forest is recent in origin and has undergone considerablechange in its range and composition throughout the lateCenozoic.     

Eucampia Index as an indicator of the Late Pleistocene oscillations of the winter sea-ice extent at the ODP Leg 119 Site 745B at the Kerguelen Plateau

A new paleoenvironmental proxy, Eucampia Index, was used to trace the Late Pleistocene oscillations of winter ice extent at ODP Leg 119, Site 745B (59° 35.71 S and 85° 51.60 E) on the Kerguelen Plateau. The index is calculated as the ratio of winter terminal to intercalary valves of the diatom Eucampia antarctica sensu lato. During the early Brunhes the winter sea-ice edge was positioned south from Site 745. It started expanding northward, closer to the site location soon after 0.4 Ma and progressed in a manner of a several wide oscillations. For approximately the last 0.1 Ma the winter sea-ice edge oscillated less and retained similar range of oscillations. The ice edge oscillated in periods which correspond closely to that of Milankovitch oscillations of Earth obliquity, although the significance of individual periods appears to vary in time.     

陕西镇安黄家湾早更新世哺乳动物群及其伴生植物

记述了发现于陕西镇安黄家湾早更新世晚期的一个大型哺乳动物群。动物群包括哺乳动物4目、11科、24种,它们是：Canis variabilis, Hyaenidae gen. et sp. indet. , Homotherium sp. , Megantereon sp. , Lynx cf. shansius , Panthera pardus , Elephantidae gen. et sp. indet. , Equus qingyangensis , Hesperotherium sinense , Ancylotherium sp. , Megatapirus augustus, Rhinocerotidae gen. et sp. indet. , Dicerorhinus lantianensis, Sus sp. , Moschus moschi ferus , Cervus unicolor , Cervus sp. 1, Cervus sp. 2, Hydropotes sp. , Capreolus sp. , Strepsiceros annectens , Leptobos sp. , Bubalus sp. 和 Budorcas taxicolor等。动物群伴生植物孢粉分析表明,当时在化石产地生长着下列植物：Selaginella sp. , Pinaceae gen. et sp. indet. , Picea sp. , Cotinus coggygria , Juglans regia , Quercus sp. , Myrica rubra , Meliaceae gen. et sp. indet. , Celtis sp. , Oleaceae ( Syringa sp. ?) gen. et sp. indet. , Chenopodiaceae gen. et sp. indet. ,Kobresia sp. , Scrophulariaceae gen. et sp. indet. , Humulus sp. , Gramineae gen. et sp. indet. , Ranunculaceae gen. et sp. indet. , Sparganium sp. ,Celastraceae gen. et sp. indet. ,Elaeagnaceae gen. et sp. indet. ,Compositae gen. et sp. indet. ,Aremisia sp. , Xanthium sibiricum 和Carex sp.等。分析了动物群生活时栖息地的气候、植被和地貌特征,结果表明,动物群栖息在温暖、湿润、有森林、灌丛草地并富有水体的生境中,当时秦岭腹地存在着相当开阔的河谷地带,山势没有现在这么险峻,因此阻断秦岭南北动物交流的天然屏障当时可能还未真正形成,秦岭南北两侧的动物可以沿着开阔的河谷地带随季节和气候的变化互相扩散迁移。