Diamonds in the desert: The discovery of Otavipithecus namibiensis

The mountains and deserts of Namibia hide many treasures—diamonds, gold, uranium, strategic minerals. But on the afternoon of June 4, 1991, we were searching Namibia's mountains for a rarer kind of stone, fossilized evidence of human evolution in southern Africa. What we found instead was the rarest “diamond” of all, one that no one had ever seen before on the African continent south of equatorial East Africa. What we found was incontrovertible evidence that prehuman “apes” were living in southern Africa millions of years before Australopithecus roamed the veld.     

Nacholapithecus skeleton from the Middle Miocene of Kenya

An almost entire skeleton of a male individual of Nacholapithecus kerioi (KNM-BG 35250) was discovered from Middle Miocene (approximately 15 Ma) sediments at Nachola, northern Kenya. N. kerioi exhibits a shared derived subnasal morphology with living apes. In many postcranial features, such as articular shape, as well as the number of the lumbar vertebrae, N. kerioi resembles Proconsul heseloni and/or P. nyanzae, and lacks suspensory specializations characteristic of living apes. Similarly, N. kerioi shares some postcranial characters with Kenyapithecus spp. However, despite the resemblance, N. kerioi and Proconsul spp. are quite different in their body proportions and some joint morphologies. N. kerioi has proportionally large forelimb bones and long pedal digits compared to its hindlimb bones and lumbar vertebrae. Its distinctive body proportions suggest that N. kerioi was more derived for forelimb dominated arboreal activities than P. nyanzae and P. heseloni. On the other hand, it exhibits a mixture of derived and primitive cranio-dental and postcranial features relative to the contemporaneous Kenyapithecus and Early MioceneMorotopithecus. While the phylogenetic position of N. kerioi is unsettled, it seems necessary to posit parallel evolution of cranio-dental and/or postcranial features in fossil and living apes.     

A cercopithecid primate from the late miocene of Molayan,Afghanistan, with remarks onMesopithecus

The first fossil primate discovered in Afghanistan comes from the Late Miocene of Molayan, Khurdkabul Basin. The materials consist of an almost-complete juvenile mandible and an isolated P₃. These two specimens do not significantly differ from thePikermi Mesopithecus pentelicus and are assigned to this species. The primate mandible from the Late Miocene of Maragheh, Iran, which has always been referred by all authors toM. pentelicus, differs from the Pikermi and Molayan materials. It must be assigned to another taxon, probably a new one. The geographic range ofM. pentelicus turns out to be considerably wider in view of the discovery of the species in Molayan, eastern Afghanistan.     

Geology and fauna of the middle Miocene hominoid site at Muruyur,Baringo district,Kenya

The middle Miocene sediments assigned to the Muruyur Beds have yielded abundant faunal remains which indicate an age somewhere near the early part of the middle Miocene, perhaps being earlier in time than Fort Ternan but probably coeval or slightly later than Maboko. Available radioisotopic age determinations suggest that the beds are between 13.5 and 14 m.y. old, which seems to be too young when compared with the biostratigraphic estimate. The importance of Muruyur Beds lies in their rich fossil content which includes hominoids of an age which is in general poorly represented in East Africa’s fossil record. This article places the fossil discoveries on record, and discusses their geological context.     

Amphibians and squamates from the middle Eocene of Namibia,with comments on pre-Miocene anurans from Africa

Three middle Eocene localities (Silica North, Silica South, Black Crow) recently discovered in Namibia have produced terrestrial faunas that rank among the few known from the period of insulation of Africa (Aptian-early Miocene). Collectively, the three localities have yielded anuran amphibians (one pipid frog, the earliest assemblage [three taxa] of ranoid frogs in Africa, one indeterminate family) and squamate reptiles (an amphisbaenian ‘lizard’, a snake that likely represents a colubroid, and two indeterminate ‘lizards’). These Eocene faunas suggest that ranoids, colubroids and African pipids are autochthonous to Africa. However, whereas pipids are vicariants inherited from West Gondwana, ranoids and colubroids (if really autochthonous) originated in Africa from unknown stems. Silica North and Silica South correspond to aquatic environments, permanent fresh water being present in the first locality; the environment of Black Crow was drier.     

Age at first molar emergence in early Miocene Afropithecus turkanensis and life-history evolution in the Hominoidea

Among primates, age at first molar emergence is correlated with a variety of life history traits. Age at first molar emergence can therefore be used to broadly infer the life histories of fossil primate species. One method of determining age at first molar emergence is to determine the age at death of fossil individuals that were in the process of erupting their first molars. This was done for an infant partial mandible of Afropithecus turkanensis (KNM-MO 26) from the approximately 17.5 Ma site of Moruorot in Kenya. A range of estimates of age at death was calculated for this individual using the permanent lateral incisor germ preserved in its crypt, by combining the number and periodicity of lateral enamel perikymata with estimates of the duration of cuspal enamel formation and the duration of the postnatal delay in the inception of crown mineralization. Perikymata periodicity was determined using daily cross striations between adjacent Retzius lines in thin sections of two A. turkanensis molars from the nearby site of Kalodirr. Based on the position of the KNM-MO 26 M(1)in relation to the mandibular alveolar margin, it had not yet undergone gingival emergence. The projected time to gingival emergence was estimated based on radiographic studies of M(1)eruption in extant baboons and chimpanzees.The estimates of age at M(1)emergence in KNM-MO 26 range from 28.2 to 43.5 months, using minimum and average values from extant great apes and humans for the estimated growth parameters. Even the absolute minimum value is well outside the ranges of extant large Old World monkeys for which there are data (12.5 to <25 months), but is within the range of chimpanzees (25.7 to 48.0 months). It is inferred, therefore, that A. turkanensis had a life history profile broadly like that of Pan. This is additional evidence to that provided by Sivapithecus parvada (Function, Phylogeny, and Fossils: Miocene Hominoid Evolution and Adaptations, 1997, 173) that the prolonged life histories characteristic of extant apes were achieved early in the evolutionary history of the group. However, it is unclear at present whether life-history prolongation in apes represents the primitive catarrhine pace of life history extended through phyletic increase in body mass, or whether it is derived with respect to a primitive, size-adjusted life history that was broadly intermediate between those of extant hominoids and cercopithecoids. Life history evolution in primates as a whole may have occurred largely through a series of grade-shifts, with the establishment of fundamental life-history profiles early in the histories of major higher taxa. These may have included shifts that were largely body mass dependent, as well as those that occurred in the absence of significant changes in body mass.     

Stratigraphic interpretation of the Kulu Formation (Early Miocene, Rusinga Island, Kenya) and its implications for primate evolution

Early Miocene fossils from Rusinga Island, Kenya, provide some of the best evidence for catarrhine evolution and diversification, and, together with more than eighty-five other mammalian species, form an important comparative reference for understanding faunal succession in East Africa. While there is consensus over the stratigraphic position of most of Rusinga's volcaniclastic deposits, the lacustrine Kulu Formation has been placed in various parts of the geological sequence by different researchers. To resolve this discrepancy, we conducted detailed geological analyses which indicate that the Kulu Formation was formed in the Early Miocene during a period of volcanic inactivity and subsidence following the early, mainly explosive hyper-alkaline phase of the Kisingiri complex and prior to the final eruptions of nephelinitic lavas. The underlying Hiwegi and older formations were locally deformed and deeply eroded before sedimentation began in the Kulu basin, so that the Kulu sediments may be significantly younger than the 17.8 Ma Hiwegi Formation and not much older than the overlying Kiangata Agglomerata-Lunene Lava series, loosely dated to ca. 15 Ma. The overall similarities between Kulu and Hiwegi faunas imply long-term ecological stability in this region. Our stratigraphic interpretation suggests that the Kulu fauna is contemporaneous with faunas from West Turkana, implying that differences between these assemblages—particularly in the primate communities—reflect paleobiogeographic and/or paleocological differences. Finally, the position of the Kulu Formation restricts the time frame during which the substantial faunal turnover seen in the differences between the primate and mammalian communities of Rusinga and Maboko Islands could have occurred.     

Avian diversity and endemism in Namibia: patterns from the Southern African Bird Atlas Project

Namibia supports a highly diverse avifauna of 644 species, including over 90 species endemic to the southern African subregion and 13 species endemic to the country. Patterns of species diversity in relation to protected areas and habitat types were analysed using data from the Southern African Bird Atlas Project. A modified Shannon index appropriate for atlas data was used to derive an index of diversity for all species, wetland, terrestrial, threatened, and regional endemic species. Species richness for Namibian endemics was mapped. Overall species diversity is highest in the northeast of Namibia where wetland and riparian habitats coincide. Both wetland and terrestrial species show highest diversity in this area. The greatest diversity of southern African endemics falls within the Savanna-Karoo systems. Several key areas are identified for red data species, including the Caprivi Strip, Kunene and Orange Rivers, coastal wetlands and ephemeral river mouths and pans. This highlights the pressures operating on wetland and riparian habitats in arid environments. Concentrations of Namibian endemics are found in the northwestern (Kaoko) escarpment of the country. Although much of the area of high diversity of wetland, terrestrial and red data species falls within protected areas, national and regional endemics are poorly represented within national parks.     

New carnivoran remains from the Late Miocene of Turkey

A great number of carnivoran remains from various late Miocene localities of Turkey, housed in the Natural History Museum of Aegean University, Bornova-Izmir, are described and compared with those from Eurasian localities for their determination. Thirteen different taxa were determined and some of them are recognized for the first time in Turkey or in their localities. Noteworthy is the presence of Dinocrocuta gigantea, which was recognized for the first time in Turkey, found in the early Vallesian locality Bayraktepe II, and the presence of the otter Sivaonyx hessicus which is a rare taxon in Eurasia, known from Eppelsheim, Germany and from Küçükçekmece and Bayraktepe II, Turkey. The hyaenid Adcrocuta cf. eximia was recognized for the first time in the Vallesian of Middle Sinap. The new determined carnivoran taxa provided some biochronological information which helps to date the localities or confirm their age.     

Late Miocene Microstonyx remains (Suidae, Mammalia) from Northern China

Several large suid cranial remains attributed to Microstonyx major are part of a new Hipparion Fauna collection from the Hezheng area, Northern China. The new material confirms the presence of Microstonyx in the late Miocene of the area. The Chinese form belongs to a small-sized eastern population with reduced premolar row and clear sexual bimodality. Statistical comparison shows that Microstonyx major was a polymorphic species and reinforces recognition of Hippopotamodon as a separate genus, defined by relatively stout premolars resulting from a different underlying pattern of allometric growth. The presence of Microstonyx in North China and the distinct suid assemblage that lived there suggest biogeographic connections between Northern China and Western Eurasia in contrast to isolation from Southern China and the Indian subcontinent. The suid fauna of the late Miocene of Northern China seems to have been restricted to the later, more humid phase represented by the Red Clay faunas.     

New Late Miocene murids from China (Mammalia, Rodentia)

New murids of Late Miocene (medial Baodean Chinese Mammal Unit) age from Inner Mongolia, northern China, and from Yunnan Province, southern China, are described. Hansdebruijnia perpusilla nov. sp. represents the earliest known and morphologically most primitive species of the genus, which is known from the latest Miocene of Europe and western Asia. The new species suggests an eastern Palaearctic origin of Hansdebruijnia. “Progonomys” yunnanensisQIU and STORCH, 1990 from Lufeng, Yunnan Province, is referred to Linomys nov. gen. New samples from Leilao, Yuanmou County, Yunnan Province, are included in this species, although this population is somewhat more primitive than that from Lufeng. Leilaomys zhudingi nov. gen. and sp. from Leilao shows a unique combination of apomorphic and plesiomorphic characters, which suggest an early divergence from the murid stem. The new findings indicate that our knowledge of the early radiation of murids in southeast Asia is still in its infancy.     

Ecostratigraphy and sequence biostratigraphy,with a neritic foraminiferal example from the Miocene in Southern Australia

The Miocene oscillation is a second order interruption of Cainozoic cooling and falling sea level with a time of warming and relatively high sea level at its zenith, the Miocene climatic optimum. The second order trajectories in putative global sea level, in oceanic δ ¹⁸O (a proxy for climate change) and δ ¹³C (a proxy for major change in nutrient regime), are punctuated by third order changes, including the Mi glacials. Southern‐temperate foraminiferal assemblages provide a profile of neritic biofacies through the oscillation. Plankton and benthos fit the second order and third order scenarios well: there are numerous resonances from the global ocean in this regional neritic realm. The cycle TB2 is a biofacies entity as well as a physical entity, and so too are most of its third order components. The influence of the Monterey carbon excursion and the climatic optimum are visible in this biotic succession. We corroborate the prediction that a trophic resource continuum expands in a warming and transgressive trend and, at the same time, responding more strongly to environmental fluctuations. We cannot corroborate the notion of coherent biofacies recurring through the succession as the environment shifts from warming to upwelling and back. There is a strong sense of a community “evolving”; through time whilst spreading and adapting ad hoc to the shifts in physical environment, rather than of discrete communities tracking those shifts.     

Dental evolution in Neophanomys (Rodentia, Octodontidae) from the late Miocene of central Argentina

The evolutionary pattern of the molar morphology of the small caviomorph (Octodontidae) Neophanomys from the late Miocene Cerro Azul Formation of central Argentina is analyzed. Two new species (chronomorphs) are recognized, which constitute an anagenetically evolving lineage with a gradual and directional pattern of increasing molar hypsodonty. Dental changes related to increasing hypsodonty are comparable to those of the octodontid lineage Chasichimys also recovered from the Cerro Azul Formation. However, Neophanomys shows comparatively less variation in gross morphology and there are no evidences that this lineage achieved euhypsodonty. In contrast, important changes in enamel microstructure (schmelzmuster) are observed among different populations of Neophanomys, supporting the hypothesis that these changes can occur at least partially independently from modifications in dental gross morphology. The patterns of dental evolution detected in the Neophanomys and Chasichimys-Xenodontomys lineages and the unequivocal polarity of the changes involved, related to increasing hypsodonty, reinforce the hypothesis that chronological differences exist among late Miocene outcroppings of Cerro Azul Formation in central Argentina.     

New discoveries of vertebrates from a near-shore marine fauna from the Early Miocene of northwestern Venezuela

New discoveries from a recently described nearshore marine fauna from northwestern Venezuela of presumed early Miocene age are reported. The fossils consist of a cranial portion of a crocodile assigned to the Tbmistominae, confirming the presence of this group in South America, and the scapula of a cetacean with affinities to the Platanistoidea. The stratigraphic section of the fossil locality ‘Cerro La Cruz’ consists of ca. 87 m of clayey marls interbedded with thin hardground units, with the upper strata being gypsiferous. The fossils were found in sandstones stratigraphically above this sequence.      

Miocene Sanitheriidae (Suiformes, Mammalia) from Namibia and Kenya: systematic and phylogenetic implications

Sanitheres are enigmatic small suoids with bunoselenodont cheek teeth and a tendency for complication of the premolars by polycuspy and polycristy. Until a few years ago virtually nothing was known about their anterior dentition, but recent discoveries in Greece, Kenya and Namibia have thrown light on their incisor and canine morphology, and reveals among other things that the canines are highly sexually dimorphic, and the dm/1 is replaced by a p/1. Material from Kipsaraman, Kenya, collected between 1997 and 2003, consists of parts of mandibles and many isolated teeth, including elements of the deciduous dentition, a significant proportion of which are unworn. These new finds confirm the aberrant nature of the sanithere dentition within a suoid framework, and support their classification as a family separate from Suidae and Palaeochoeridae (= Old World Tayassuidae).

Résumé

Les sanithères sont de petits Suoïdes aux dents jugales bunosélénodontes avec des prémolaires qui présentent une tendance à la multiplication des cuspides et des crêtes (“polycuspidie” et la “polycristie”). Jusqu’à récemment, on ne connaissait rien sur la morphologie de leur dentition antérieure, mais des découvertes récentes réalisées en Grèce, au Kenya et en Namibie, lèvent le voile sur la morphologie de leurs incisives et de leur canine. Ainsi, il apparaît que les canines sont très dimorphes et que la dm/1 inférieure est remplacée par une p/1. Le matériel de Kipsaraman au Kenya, récolté entre 1997 et 2003, consiste en des fragments de mandibules et de nombreuses dents isolées, dont des dents déciduales, qui pour la plus grande part ne sont pas usées. Ces nouveaux fossiles confirment la nature aberrante de la dentition des sanithères au sein des Suoidea, et supporte leur classification dans une famille distincte des Suidae, et des Palaeochoeridae (= Tayassuidae de l’Ancien Monde).     

New Data on Miocene Neotropical Provinciality from Cerdas, Bolivia

We provide the first faunal report for the early/middle Miocene fauna of Cerdas, Bolivia (16.5–15.3 Ma; 20° 52′ S, 66° 19′ W), based primarily on new specimens collected in 2007. As many as twelve species of mammals in nine families are represented. Notoungulates include Palyeidodon obtusum (Toxodontidae), Protypotherium cf. attenuatum and Protypotherium sp. nov. (Interatheriidae), ‘Plesiotypotherium’ minus and possibly Microtypotherium choquecotense (Mesotheriidae), and Hegetotherium? sp. nov. (Hegetotheriidae). Xenarthrans include Stenotatus planus and Prozaedyus sp. (Cingulata: Dasypodidae), Peltephilidae gen. et sp. nov. (Cingulata), and Xyophorus cf. bondesioi (Pilosa: Nothrotheriidae). A new species of litoptern is also present (Macraucheniidae) as well as an unidentified rodent (Chinchillidae: Lagostominae). Two of these Cerdas species occur in Friasian sensu stricto/Colloncuran SALMA faunas of Patagonia, and perhaps one in Santacrucian SALMA faunas. Among middle latitude localities, Cerdas resembles Chucal, Chile (late early Miocene, Santacrucian SALMA) in community composition (e.g., abundant mesotheriids, few rodent species), but has no species in common; it shares one species with Quebrada Honda, Bolivia (middle Miocene, Laventan SALMA), and perhaps as many as three more. These observations indicate that Cerdas is not referable to the Santacrucian, and that the upper limit of this SALMA in the middle latitudes falls somewhere between 17.5 Ma (the top of Chucal) and 16.5 Ma (the base of Cerdas). Based on the range of dates proposed for the youngest Santacrucian intervals in Patagonia, a diachronous offset of up to 2.1 Ma may exist at this point in the SALMA sequence between middle and high latitude faunas.