Academic literature on the topic 'Fossils - Namibia'

A method is presented for the digital reconstruction of weakly calcified fossils within the Nama Group, Namibia. These recently described fossils (Grotzinger et al. 2000) are preserved as calcitic void-fill in a calcite matrix, and individual specimens cannot be freed by conventional techniques. The technique presented here has several integrated steps: (1) the analysis of cross-sections of fossil specimens, (2) the construction of a three-dimensional “tomographic” model that is assembled from the cross-sections, (3) the development of an idealized mathematical model based upon geometric parameters measured from the tomographic model, and (4) the visualization of randomly oriented cross-sections through the mathematical model, which can be compared with fossil cross-sections in outcrop.In this procedure, rocks containing the fossils are ground and digitally photographed at thickness intervals of 25 μm. A battery of image-processing techniques is used to obtain the contour outlines of the fossils in serial cross-sections. A Delaunay triangulation method is then used to reconstruct the morphology from tetrahedrons which connect the contours in adjacent layers. We found that most of the fossils represent a single morphology with some well-defined characters that vary slightly among individual specimens. This fossil morphology was described by Grotzinger et al. (2000) as Namacalathus hermanastes. A mathematical description of the morphology is used to obtain a database of randomly oriented synthetic cross-sections. This database reproduces the vast majority of cross-sections observed in outcrop.

Owing to the lack of temporally well-constrained Ediacaran fossil localities containing overlapping biotic assemblages, it has remained uncertain if the latest Ediacaran ( ca 550–541 Ma) assemblages reflect systematic biological turnover or environmental, taphonomic or biogeographic biases. Here, we report new latest Ediacaran fossil discoveries from the lower member of the Wood Canyon Formation in Nye County, Nevada, including the first figured reports of erniettomorphs, Gaojiashania , Conotubus and other problematic fossils. The fossils are spectacularly preserved in three taphonomic windows and occur in greater than 11 stratigraphic horizons, all of which are below the first appearance of Treptichnus pedum and the nadir of a large negative δ 13 C excursion that is a chemostratigraphic marker of the Ediacaran–Cambrian boundary. The co-occurrence of morphologically diverse tubular fossils and erniettomorphs in Nevada provides a biostratigraphic link among latest Ediacaran fossil localities globally. Integrated with a new report of Gaojiashania from Namibia, previous fossil reports and existing age constraints, these finds demonstrate a distinctive late Ediacaran fossil assemblage comprising at least two groups of macroscopic organisms with dissimilar body plans that ecologically and temporally overlapped for at least 6 Myr at the close of the Ediacaran Period. This cosmopolitan biotic assemblage disappeared from the fossil record at the end of the Ediacaran Period, prior to the Cambrian radiation.

Ediacara-type fossils are rare in the southwestern United States, and Cambrian occurrences of soft-bodied Ediacaran-type fossils are extremely rare. We report both discoidal and frondlike fossils comparable to Ediacaran taxa from the western edge of the Great Basin. We describe one specimen of a discoidal fossil, referred to the form species ?Tirasiana disciformis, from the upper member of the Lower Cambrian Wood Canyon Formation from the Salt Spring Hills, California. Two fragmentary specimens of frond-like soft-bodied fossils are described from the middle member of the Lower Cambrian Poleta Formation in the White Mountains, California, and the upper member of the Wood Canyon Formation in the southern Kelso Mountains, California. On the basis of similarities with fossils from the lower member of the Wood Canyon Formation and from the Spitzkopf Member of the Urusis Formation of Namibia, these specimens are interpreted as cf. Swartpuntia. All fossils were collected from strata containing diagnostic Early Cambrian body and trace fossils, and thus add to previous reports of complex Ediacaran forms in Cambrian marine environments. In this region, Swartpuntia persists through several hundred meters of section, spanning at least two trilobite zones.

Abundant tubular macrofossils occur in finely laminated siltstones and shales of the 548–542 Ma Schwarzrand Subgroup, Nama Group, Namibia. The Nama tubes occur in both the Vingerbreek and Feldschuhhorn members commonly in dense populations and always in fine-grained, lower shore-face lithologies deposited below fair-weather wave base. The tubes are preserved mostly as compressed casts and molds that range in width from 0.6 to 2.1 mm; apparently incomplete specimens reach lengths up to 10 cm. All specimens show sinuous bending and occasional brittle fracture, indicating an original construction of strong but flexible organic matter. Feldschuhhorn specimens preserve fine longitudinal pleats or folds that record pliant organic walls, but the older Vingerbreek populations do not. Similarly, some specimens in the Feldschuhhorn Member display branching, while Vingerbreek tubes do not. The abundant Feldschuhhorn tubes are assigned to the widespread Ediacaran problematicum Vendotaenia antiqua; however, the distinctive Vingerbreek population remains in open nomenclature. The most abundant fossils in Nama rocks, these tubes resemble populations in Ediacaran successions from Russia, China, Spain, and elsewhere. Beyond their local importance, then, such tubes may turn out to be the most abundant record of Ediacaran life.

Reefs containing abundant calcified metazoans occur at several stratigraphic levels within carbonate platforms of the terminal Proterozoic Nama Group, central and southern Namibia. The reef-bearing strata span an interval ranging from approximately 550 Ma to 543 Ma. The reefs are composed of thrombolites (clotted internal texture) and stromatolites (laminated internal texture) that form laterally continuous biostromes, isolated patch reefs, and isolated pinnacle reefs ranging in scale from a meter to several kilometers in width. Stromatolite-dominated reefs occur in depositionally updip positions within carbonate ramps, whereas thrombolite-dominated reefs occur broadly across the ramp profile and are well developed as pinnacle reefs in downdip positions.The three-dimensional morphology of reef-associated fossils was reconstructed by computer, based on digitized images of sections taken at 25-micron intervals through 15 fossil specimens and additionally supported by observations of over 90 sets of serial sections. Most variation observed in outcrop can be accounted for by a single species of cm-scale, lightly calcified goblet-shaped fossils herein described as Namacalathus hermanastes gen. et sp. nov. These fossils are characterized by a hollow stem open at both ends attached to a broadly spheroidal cup marked by a circular opening with a downturned lip and six (or seven) side holes interpreted as diagenetic features of underlying biological structure. The goblets lived atop the rough topography created by ecologically complex microbial-algal carpets; they appear to have been sessile benthos attached either to the biohermal substrate or to soft-bodied macrobenthos such as seaweeds that grew on the reef surface. The phylogenetic affinities of Namacalathus are uncertain, although preserved morphology is consistent with a cnidarian-like bodyplan. In general aspect, these fossils resemble some of the unmineralized, radially symmetric taxa found in contemporaneous sandstones and shales, but do not appear to be closely related to the well-skeletonized bilaterian animals that radiated in younger oceans. Nama reefs demonstrate that biohermal associations of invertebrates and thrombolite-forming microorganisms antedate the Cambrian Period.

Ediacaran fossils are taphonomically similar to impressions of fossil plants common in quartz sandstones, and the relief of the fossils suggests that they were as resistant to compaction during burial as some kinds of Pennsylvanian tree trunks. Fossils of jellyfish are known from siderite nodules and fine-grained limestone, and even in these compaction-resistant media were more compressed during burial than were the Vendobionta. Vendobionta were constructed of materials that responded to burial compaction in a way intermediate between conifer and lycopsid logs. This comparative taphonomic study thus falsifies the concept of Vendobionta as thin soft-bodied creatures such as worms and jellyfish.Lichens, with their structural chitin, present a viable model for the observed preservational style of Vendobionta, as well as for a variety of other features that now can be reassessed from this new perspective. The diversity of Ediacaran body plans can be compared with the variety of form in fungi, algae, and lichens. The large size (ca. 1 m) of some Ediacaran fossils is reasonable for sessile photosynthetic symbioses, and much bigger than associated burrows of metazoans not preserved. Microscopic tubular structures and darkly pigmented cells in permineralized late Precambrian fossils from Namibia and China are also compatible with interpretation as lichens. The presumed marine habitat of Ediacaran fossils is not crucial to interpretation as lichens, because fungi and lichens live in the sea as well as on land.

Here we describe large, complex trace fossils in the late Ediacaran Omkyk Member of the Zaris Formation, Nama Group, southern Namibia. The horizontal trace fossils are preserved on a number of talus blocks from a bedding plane of a cm-thick sandstone lens from a single stratigraphic horizon less than 100 m below an ash bed dated at 547.3 ± 0.7 Ma. The forms consist of overlapping U-shaped spreiten elements with parallel limbs surrounded by an outer tube. Individual U-shaped elements are 0.2 to 1 cm in diameter, the outer tube is less than 3 mm in diameter, and the forms as a whole range from 5 to 30 cm long and 3 to 10 cm wide. The specimens commonly show a change in direction and change in diameter. The morphology of these trace fossils is comparable to backfill structures, particularly specimens of Paleozoic Zoophycos from shallow water environments. Here we interpret these horizontal spreiten-burrows to record the grazing of the trace-maker on or below a textured organic surface. The identification of large late Ediacaran trace fossils is consistent with recent reports of backfilled horizontal burrows below the Precambrian–Cambrian boundary and is suggestive of the appearance of complex feeding habits prior to the Cambrian trace fossil explosion.

Cette thèse présente les données des pollens et micro-charbons fossiles couvrant la période des 50 000 dernières années à partir de sites sélectionnés transversalement nord-sud du désert de Namib. Dans le cadre de cette thèse, on utilise le rock hyrax middens, l’accumulation des boulettes et des urines fossilisés du Procavia capensis, représentant une excellente archive pour archives pour la préservation des pollens et micro-charbons à long-terme. Trois sites des hyrax middens ont été sélectionnés pour l'analyse: au sud du désert de Namib (Pella), la marge est des dunes de sable de Namib (Zizou) et le centre de la Namib (Spitzkoppe). En plus, le régime pluvial de ces sites se caractérise par une forte variabilité annuelle et interannuelle. En conséquence, tous ces sites se situent au long de l’écotone du Désert et du biome Nama-Karoo, ainsi qu'à l’est (biome de Savane). Alors que ces sites sont répertoriés dans des écosystèmes similaires, l’écotone, lui, est considéré comme une zone potentiellement très sensible au changement du système climatique régional. Un intérêt spécifique de ces enregistrements terrestres est pour évaluer s’ils corroborent ou s’opposent avec les résultats provenant ceux des sédiments marins de la côte namibienne, en particulier la conclusion : l’abondance des taxa dominants du Fynbos Biome du Cape peut indiquer significativement une expansion vers le nord de la flore du Cape pendant les périodes plus froides glaciaires. Selon les sites d’études sélectionnées, les conclusions principales de ce travail sont les suivantes:Les hyrax middens de Pella fournissent le premier enregistrement pollinique continué au sud du désert de Namib durant la période des 50 000 dernières années. Ces données polliniques ont permis de reconstruire le changement de la végétation et d'estimer la température et l'aridité. Les résultats indiquent que la période glaciaire se caractérise par une augmentation de la disponibilité de l'eau sur le site par rapport à l'Holocène. Les changements de la température et de l'évapotranspiration potentielle semblent avoir joué un rôle important dans la détermination de l'équilibre hydrologique.L'enregistrement de Zizou hyrax midden met en évidence des changements de la végétation à la marge l'est des dunes de sable depuis 38 000 ans cal BP. La végétation de la période glaciaire se caractérise par les pourcentages relativement élevés des Astéracées pollen, et plus particulièrement par des taxa du climat plus froid: Stoebe et Artemisia¬-type. En accord avec les données de Pella, le réchauffement au début de l'Holocène indiqué par la dominance de pollen des graminées dans l'assemblage pollinique suggère une expansion du biome de Désert.Les hyrax middens de Spitzkoppe enregistrent les changements de la végétation dans le centre du désert de Namib au cours des 32 000 dernières années. Les résultats sont globalement cohérents en comparant aux autres enregistrements terrestres dans la région. L'analyse de ces données n'est cependant pas encore terminée.Dans tous ces sites, une variabilité significative a été observée à la fois dans la dernière période glaciaire et l'Holocène. Les conditions plus froides de l'ère glaciaire semblent être caractérisées par une augmentation de la disponibilité de l'eau le long de la totalité de notre zone d'étude. Au contraire des résultats provenant des carottes marines, nos enregistrements indiquent aucune expansion de la végétation de Fynbos biome, et seulement des traces de Restionaceae pollen dans le site extrêmement au sud à Pella (pas plus de 1%), mais aucun trace de ce pollen n'ayant été observé à Zizou ainsi qu’à Spitzkoppe
This thesis presents fossil pollen and microcharcoal data during the last 50,000 years from a north-south transect of the Namib Desert. The arid environment of the Namib precludes the development of permanent wetlands, and as a result few palaeoenvironmental records exist from the region. In this study, we employ rock hyrax middens – fossilised accumulations of the faecal pellets and urine of the Procavia capensis. Hyrax middens from three sites were selected for analysis: the southern Namib (Pella), the eastern margin of Namib Sand Sea (Zizou), and the central Namib (Spitzkoppe). The results from these terrestrial sites are the extent to which they may corroborate or conflict with findings from pollen records obtained from marine sediments of the Namibian coast.The Pella hyrax middens provide the first continuous pollen record from the southern Namib Desert since the last 50,000 years, and are used to reconstruct vegetation change and quantitative estimates of temperature and aridity. Results indicate that the last glacial period was characterised by increased water availability relative to the Holocene. Changes in temperature and potential evapotranspiration appear to have played a significant role in determining the hydrologic balance. The record can be considered in two sections: 1) the last glacial period, when low temperatures favoured the development of more mesic Nama-Karoo vegetation at the site, with periods of increased humidity concurrent with increased coastal upwelling, both responding to lower global/regional temperatures; and 2) the Holocene, high temperatures and potential evapotranspiration resulted in increased aridity and an expansion of the Desert Biome.Considered in the context of discussions of forcing mechanisms of regional climate change and environmental dynamics, the results from Pella stand in clear contrast with many inferences of terrestrial environmental change derived from regional marine records. Observations of a strong precessional signal and interpretations of increased humidity during phases of high local summer insolation in the marine records are not consistent with the data from Pella. Similarly, while high percentages of Restionaceae pollen has been observed in marine sediments during the last glacial period, they do not exceed 1% of the assemblage from Pella, indicating that no significant expansion of the Fynbos Biome has occurred during the last 50,000 years.The Zizou hyrax midden highlights vegetation changes on the eastern margin of the Namib Sand Sea since 38,000 cal BP. Results show the different vegetation compositions between the last glacial period and the Holocene. Glacial vegetation characterised with relatively high percentages of Asteraceae pollen, particularly cool climate taxa such as Stoebe and Artemisia types. Similar to the data from Pella, with the onset of Holocene warming grass pollen comes to dominate the assemblage, suggesting an expansion of the Desert Biome. We suggest that the climate during the last glacial period was more humid, and supported the development of shrubs/small trees. Arid conditions during the Holocene saw the depletion of this resource, and the development of grasslands that could exploit the rare rains that the region experiences today. In common with the Pella record, no elements of the Cape flora are found in the Zizou middens.The Spitzkoppe hyrax middens record vegetation changes in the central Namib during the last 32,000 years. The last glacial vegetation compositions composed of Olea, Artemisia¬-type, Stoebe¬-type and grasses. In the Holocene, the arboreal taxa such as Olea was replaced by others like Eculea, Dombeya, Commiphora, and Croton¬-type with relative higher percentage of grasses at early Holocene

Fossil fish scales hold potential for ellucidating past fish population fluctuations. A system of classification for scales from the pilchard, Sardinops ocellata, and the anchovy, Engraulis capensis, is presented. Both species show an unexpected range of scale types. The classifications reduce errors in distinguishing between the scales of the two species to ±2,5%. Scale loss from these fish is quantified under laboratory conditions. Pilchard lose 1,56 scales/fish/day due to death and 1,50 scales/fish/day due to deciduousness over their expected lifetimes. For anchovy the figures are 2,42 scales/fish/day (death) and 0,48 scales/fish/day (deciduousness). Application of these scale-loss studies to scales preserved in the anaerobic sediments off Walvis Bay, Namibia, shows that deciduousness is the dominant process contributing scales to the sediments. This basic information on pilchard and anchovy scale loss is used to interpret counts of scales in the laminated interval of a core taken from the diatomaceous muds off Walvis Bay. This pilot study shows that: i) the Namibian Fishery was dominated by pilchard in the past as it was prior to the collapse in the early 1970's and, because of this, is distinctly different from the anchovy/anchovetta-dominated east Pacific systems; and ii) major pre-fishery stock fluctuations do appear to be reflected in the sedimentary record. Further scale studies on larger sediment samples are recommended to ellucidate the Namibian fish stock fluctuations.

The locality of Zwartbas is situated at the border of Namibia and South Africa about 15 km west of Noordoewer. The mapped area is confined by the Tandjieskoppe Mountains in the north and the Orange River in the south. Outcropping rocks are predominantly sediments of the Nama Group and of the Karoo Supergroup. During the compilation of this paper doubts arose about the correct classification of the Nama rocks as it is found in literature. Since no certain clues were found to revise the classification of the Nama rocks, the original classification remains still valid. Thus the Kuibis and Schwarzrand Subgroup constitute the Nama succession and date it to Vendian age. A glacial unconformity represents a hiatus for about 260 Ma. This is covered by sediments of the Karoo Supergroup. Late Carboniferous and early Permian glacial deposits of diamictitic shale of the Dwyka and shales of the Ecca Group overlie the unconformity. The shales of the Dwyka Group contain fossiliferous units and volcanic ash-layers. A sill of the Jurassic Tandjiesberg Dolerite Complex (also Karoo Supergroup) intruded rocks at the Dwyka-Ecca-boundary. Finally fluvial and aeolian deposits and calcretes of the Cretaceous to Tertiary Kalahari Group and recent depositionary events cover the older rocks occasionally
Die Lokalität Zwartbas liegt an der namibisch-südafrikanischen Grenze, etwa 15 km westlich von Noordoewer. Das Kartiergebiet wird durch die Tandjiesberge im Norden und den Oranje Fluß im Süden begrenzt. Die anstehenden Gesteine bestehen hauptsächlich aus Sedimenten der Nama Gruppe und der Karoo Supergruppe. Während der Erarbeitung dieser Abhandlung entstanden Zweifel an der Klassifikation der Nama Gesteine, so wie sie in der Literatur zu finden ist. Da keine sicheren Hinweise zur Revision der Klassifikation der Nama Gesteine gefunden wurden, bleibt die ursprünglich Klassifikation jedoch gültig. Die Kuibis und Schwarzrand Untergruppe bilden also die Nama Abfolge und datieren sie ins Vendian. Eine glaziale Diskontinuität repräsentiert einen Hiatus von etwa 260 Mio Jahren. Sie wird überlagert von Sedimenten der Karoo Supergruppe. Spät-karbone und früh-permische glaziale Ablagerungen von diamiktitischen Tonsteinen der Dwyka Gruppe und Tonsteine der Ecca Gruppe liegen über dieser Diskontinuität. Die Sedimente der Dwyka Gruppe sind fossilführend und enthalten Tufflagen. Ein Sill des jurassischen Tandjiesberg Dolerit Komplex (auch Karoo Supergruppe) intrudierte in die Gesteine an der Dwyka-Ecca Grenze. Schließlich bedecken lokal fluviatile und äolische Ablagerungen und Kalkkrusten der kretazischen und tertiären Kalahari Gruppe und jüngerer Ablagerungsereignisse die älteren Gesteine

Thin, pyroclastic marker beds are preserved in argillaceous units of the Dwyka Group in southern Nambia and South Africa which are the earliest witnesses of volcanism in Karoo-equivalent strata of southern Africa. The aim of this study is to present the field appearance of these marker beds, to characterise their mineralogy, geochemistry and heavy mineral contents and to present new radiometric age data from their juvenile zircons. Carboniferous-Permian Karoo deposits in the Aranos Basin of southern Namibia include the glacially dominated, Carboniferous Dwyka Group and the shelf sediments of the overlying Permian Ecca Group. The Dwyka Group can be subdivided into four upward-fining deglaciation sequences, each capped by relatively fine-grained glaciolacustrine or glaciomarine deposits. The uppermost part of the second deglaciation sequence comprises a thick fossiliferous mudstone unit, referred to as the ”Ganigobis Shale Member”. An abundance of marine macro- and ichnofossils as well as extrabasinally derived ashfall tuff beds characterise the more than 40 m thick mudstones and provide the basis for an integrated high-resolution biostratigraphic and tephrostratigraphic framework. The Ganigobis Shale Member contains remains of paleoniscoid fishes, bivalves, gastropods, scyphozoa, crinoid stalks, sponges and sponge spicules, radiolaria, coprolites and permineralised wood. These mostly marine body and trace fossils record the extent of the first of a series of marine incursions into the disintegrating Gondwanan interior as early as the Carboniferous. Within the Ganigobis Shale Member 21 bentonitic tuff beds displaying a thickness of 0.1 and 2.0 cm were determined which in part can be traced laterally over tens of kilometres indicating an ashfall derivation. Further bentonitic tuff beds of the Dwyka Group were detected in cut banks of the Orange River near Zwartbas in the Karasburg Basin (southern Namibia). The 65 tuff beds vary between 0.1 and 4.0 cm in thickness. Due to a similar fossil content and age of the background deposits, the tuff beds are thought to have originated from the same source area as those from the Aranos Basin. Thin-sections reveal the derivation of the tuff beds as distal fallout ashes produced by explosive volcanic eruptions. The matrix consists of a micro- to cryptocrystalline clay mineral-quartz mixture. Rare fragments of splinter quartz, completely recrystallized ash-sized particles of former volcanic glass and few apatite and zircon grains are the only juvenile components. The tuff beds contain as non-opaque, juvenile heavy minerals mostly zircon, apatite, monazite and sphene but also biotite, garnet, hornblende and tourmaline. Geochemical analyses point to an original, intermediate to acid composition of the tuff samples. LREE enrichment and Eu-anomalies show that the parent magma of the tuff beds was a highly evolved calc-alkaline magma. Tectonomagmatic discrimination diagrams point to a volcanic arc setting. Bedding characteristics and the lack of any Carboniferous-Permian volcanic successions onshore Namibia makes an aeolian transport of the ash particles over larger distances likely. Siliceous ashes could thus have been transported by prevailing south-westerly winds from arc-related vents in South America to southern Africa. A second, more local source area could have been located in an intracontinental rift zone along the western margin of southern Africa which is indicated by north-south directed ice-flow directions in the Late Carboniferous. SHRIMP-based age determinations of juvenile magmatic zircons separated from the tuff beds allow a new time calibration of Dwyka Group deglaciation sequences II - IV and the Dwyka/Ecca boundary. Zircons of the Ganigobis Shale Member yield SHRIMP-ages of 302-300 Ma. This dates the uppermost part of the second deglaciation sequence in southern Namibia to the Late Carboniferous (Gzelian) and provides a minimum age for the onset of Karoo-equivalent marine deposition. The age of the uppermost argillaceous part of the third deglaciation sequence (297 Ma) was determined from zircons of a tuffaceous bed sampled in a roadcut in the Western Cape Province, South Africa. The deposits correlate with the Hardap Shale Member in the Aranos Basin of southern Namibia which are part of much more widespread Eurydesma transgression. The age of the Dwyka/Ecca boundary was determined by SHRIMP-measurements of juvenile zircons from two tuff beds of the basal Prince Albert Formation sampled in the Western Cape Province (South Africa). The zircons revealed ages of 289 - 288 Ma which date the Dwyka/Ecca boundary at about 290 Ma. According to these ages, deglaciation sequences II-IV lasted for 5 Ma on average
Geringmächtige, bentonitische Tuffe treten in Tonsteinabschnitten der karbonen Dwyka Gruppe im südlichen Namibia und Südafrika auf. Sie repräsentieren die ersten Hinweise auf eine vulkanische Tätigkeit innerhalb der Karoosedimente im südlichen Afrika. Die vorliegende Dissertation faßt die Geländebeschreibung der Tuffe, ihre Petrographie, Mineralogie und Geochemie zusammen. Juvenile Zirkone der Tuffe erlaubten eine radiometrisches Altersermittlung mittels SHRIMP-Analyse. Sie stellen somit die ersten radiometrisch exakt ermittelten Altersdaten innerhalb der Dwyka Gruppe dar. Permokarbone Karoosedimente des Aranos Beckens in Südnamibia setzen sich aus der glazigenen Dwyka Gruppe des Karbons und den Schelfsedimenten der folgenden Ecca Gruppe des Perms zusammen. Die Dwyka-Gruppe kann dabei in vier Entgletscherungssequenzen unterteilt werden. Der oberste Bereich jeder Entgletscherungssequenz ist meist durch glaziomarine Ablagerungen gekenn-zeichnet. Im Fall der zweiten Entgletscherungssequenz handelt es sich um einen mehr als 40 m mäch-tigen, fossilführenden Tonsteinabschnitt, der als ‘Ganigobis Shale Member’ bekannt ist. Eine Vielzahl von meist marinen Makro- und Spurenfossilien (palaeoniskoide Fischen, Bivalven, Gastropoden, Scyphozoen, Crinoideenstielglieder, Radiolarien) sowie distale Aschentuffe bilden die Grundlage für eine hochauflösende, biostratigraphische und tephrostratigraphische Gliederung des ‘Ganigobis Shale Members’. 21 bentonitische, lateral verfolgbare Aschentuffe mit einer Mächtigkeit zwischen 0.1 und 2.0 cm wurden innerhalb des ‘Ganigobis Shale Member’ bestimmt. 65 weitere, bis 4.0 cm mächtige Aschentuffe der Dwyka Gruppe wurden in Uferbänken des Orange Rivers in der Nähe von Zwartbas im Karasburg Becken Südnamibias entdeckt. Aufgrund eines ähnlichen Fossilinhaltes der Hinter-grundsedimente und eines ähnlichen Alters der Tuffe kann von dem gleichen Herkunftsgebiet der Aschen ausgegangen werden. Dünnschliffe der Tuffe zeigen, daß es sich bei den Horizonten um distale Aschenfallablagerungen handelt, die durch explosiven Vulkanismus gefördert wurden. Die Matrix besteht aus einer mikro- bis kryptokristallinem Tonmineral-Quarz- Mischung. Idiomorpher, hexagonaler Quarz, Splitterquarze und Quarzfragmente, vollständig rekristallisierte Aschenkörner und vereinzelt Schwerminerale wie Apatit und Zirkon sind weitere juvenile Komponenten. Folgende transparente, juvenile Schwerminerale treten auf: Zirkon, Apatit, Monazit, Titanit, Biotit, Granat, Hornblende und Turmalin. Geochemische Analysen weisen auf eine intermediäre bis saure Ausgangszusammensetzung der Tuffe hin. Die Anreicherung der LREE und die Eu-Anomalien zeigen, daß die Zusammensetzung des Ausgangsmagma der Tuffe kalkalkalisch und sehr differenziert war. Tektonomagmatische Diskrimi-nationsdiagramme deuten eine Subduktionszone als Herkunftsgebiet der Tuffe an. Die Korngröße der Tuffe und das Fehlen jeglicher permokarboner, vulkanischer Abfolgen in Namibia läßt auf einen Transport der Aschen über größere Distanzen schließen. Saure Aschen könnten bei vorherrschenden südwestlichen Windrichtungen von Südamerika, wo saurer Inselbogenmagmatismus im Permokarbon bekannt ist, nach Südafrika und Namibia transportiert worden sein. Ein zweites, lokaleres Herkunfts-gebiet der Aschentuffe könnte innerhalb einer kontinentalen Riftzone am Westrand des südlichen Afrikas gelegen haben. Sie ist im Oberkarbon durch allgemein nord-südgerichtete Eisstromrichtungen im Aranos und Karasburg Becken (Südnamibia) und im Perm durch die marinen Ablagerungen der Whitehill Formation (Ecca Gruppe) angedeutet. Altersbestimmungen an den juvenilen Zirkonen ermöglichten sowohl eine neue Zeiteinschätzung der Entgletscherungssequenzen II - IV innerhalb der Dwyka Gruppe als auch eine zeitliche Neukali-brierung der Dwyka-/Ecca Grenze. Datierte Zirkone aus Tuffen des Ganigobis Shale Members ergaben SHRIMP-Alter von 302 - 300 Ma. Damit fallen der oberste Bereich der zweiten Entgletscherungssequenz und die in den marinen enthaltenen Fossilien in das Oberkarbon (Gzelian). Das Alter des Topbereichs der dritten Entgletscherungssequenz (297 Ma) wurde an Zirkonen einer tuffitischen Schicht aus der Provinz Westkap in Südafrika bestimmt. Die dort aufgeschlossenen Ablagerungen korrelieren mit dem Hardap Shale Member im Aranos Becken Süd-namibias und sind Teil der weltweit bekannten Eurydesma - Transgression. Das Alter der Dwyka / Ecca-Grenze wurde an juvenilen Zirkonen von Tuffen der basalen Prince Albert Formation (Ecca Gruppe) in der Provinz Westkap (Südafrika) bestimmt. Die U-Pb - Messungen an den Zirkonen ergaben Alter von 289 - 288 Ma, die die Dwyka / Ecca-Grenze bei circa 290 Ma festlegen

At Zwartbas, about 10 km west of Vioolsdrif, southern Namibia, the Dwyka succession is composed of tillites and distal fossiliferous dropstone-bearing glacio-marine shales. The completely exposed Dwyka succession is interbedded with thin bentonites, altered distal pyroclastic deposits, which were derived from the magmatic arc at the southern rim of Gondwana. Dropstone-bearing and dropstonefree sequences intercalate with four diamictites, of which the two lowest were certainly recognised as tillites. Four events of deglaciation were proven at Zwartbas and thus consist with correlative deposits in southern Africa. Numerous fossilised fishes, trace fossils, and plant fragments appear frequently within the lower half of the Dwyka succession whereas trace fossils were principally found in the complete succession. Although the environmental determination is quite problematic, the fossil assemblage rather implies proximal, shallow water conditions with temporary restricted oxygenation. The hinterland was covered with considerable vegetation, which points to a moderate climate. Water salinity determinations based on shale geochemistry rectify contrary palaeontological results and point to rather brackish or non-marine conditions in comparison to present-day salinites. Geochemical analyses of the bentonites relate the pyroclastic deposits with acid to intermediate source magmas, as they are known from the magmatic arc in present-day Patagonia. Tectono-magmatic comparisons furthermore emphasise a syn-collision or volcanic-arc situation of the magma source. However, significant cyclicity in the production of the pyroclastic deposits was not observed. Radiometric age determinations of two tuff beds clearly date the onset of glacial activity into the Late Carboniferous.

AbstractIt is traditionally held that early hominins of the genusAustralopithecushad a foot transitional in function between that of the other great apes and our own but that the appearance of genusHomowas marked by evolution of an essentially biomechanically modern foot, as well as modern body proportions. Here, we report the application of whole foot, pixel-wise topological statistical analysis, to compare four populations of footprints from across evolutionary time:Australopithecusat Laetoli (3.66 Ma, Tanzania), early AfricanHomofrom Ileret (1.5 Ma, Kenya) and recent modern (presumptively habitually barefoot) pastoralistHomo sapiensfrom Namibia (Holocene), with footprints from modern Western humans. Contrary to some previous analyses, we find that only limited areas of the footprints show any statistically significant difference in footprint depth (used here as an analogy for plantar pressure). A need for this comparison was highlighted by recent studies using the same statistical approach, to examine variability in the distribution of foot pressure in modern Western humans. This study revealed very high intra-variability (mean square error) step-to-step in over 500 steps. This result exemplifies the fundamental movement characteristic of dynamic biological systems, whereby regardless of the repetition in motor patterns for stepping, and even when constrained by experimental conditions, each step is unique or non-repetitive; hence, repetition without repetition. Thus, the small sample sizes predominant in the fossil and ichnofossil record do not reveal the fundamental neurobiological driver of locomotion (variability), essentially limiting our ability to make reliable interpretations which might be extrapolated to interpret hominin foot function at a population level. However, our need for conservatism in our conclusions does not equate with a conclusion that there has been functional stasis in the evolution of the hominin foot.