Miocene-Pliocene Vegetation change in south-western Africa (ODP Site 1081, offshore Namibia)
Authors:
Hoetzel et al
Abstract:
Aridification is an important component of Late Neogene climate change in south-western Africa probably caused by modifications in the atmospheric circulation in relation to the initiation and intensification of the Benguela Upwelling System due to globally steepening of the meridional pressure gradient. Intensification of the meridional pressure gradient influenced the climate intensively which had then an impact on the vegetation. However, vegetation changes of south-western Africa from the Miocene to Pliocene have not yet been reported and only indirectly investigated by sedimentological data. Here, we present a pollen record of marine ODP Site 1081 retrieved 160 km offshore Namibia covering the time between 9 and 2.7 Ma. Using an endmember unmixing model we distinguished three vegetation phases: a relative wet phase, during the Tortonian, showing higher representations of Cyperaceae, a transition phase during the Messinian, when especially grasses expanded, and a dry one covering the Pliocene with a strong representation of desert and semi-desert plants. The three phases indicate ongoing aridification probably caused by intensified meridional pressure gradients. Additionally, aquatic vegetation indicators appear in our pollen record from around 5 Ma on, which we attribute to a relocation of the lower course of the Cunene River to its modern outlet in the Atlantic Ocean. Redirection of the Cunene River toward the Atlantic would have deprived the palaeolake Cunene of an important source of fresh-water ultimately resulting in desiccation of the lake and the formation of the Etosha Pan.
Showing posts with label namibia. Show all posts
Showing posts with label namibia. Show all posts
Friday, February 20, 2015
Evidence of Namibia's Neogene Aridification From Offshore Samples
Labels:
africa,
Cenozoic,
miocene,
namibia,
neogene,
paleobotany,
paleoclimate,
paleoenvironment,
Pliocene,
pollen
Monday, September 22, 2014
Evidence of Ridge Subduction From Ediacaran NeoProterozoic Namibia
Fingerprints of late Neoproterozoic ridge subduction in the Pan–African Damara belt, Namibia
Authors:
Meneghnini et al
Abstract:
Subduction of mid-ocean ridges is a common feature in recent convergent margins, but is rarely documented in Proterozoic to Paleozoic orogenic belts. Here we describe evidence for ridge-trench interaction in the deeply eroded late Neoproterozoic Damara orogenic belt, central Namibia. The earliest interaction is indicated by primary intrusive contacts between amphibolite facies mid-ocean ridge metabasalts and trench metasediments. U-Pb zircon ages of 550–540 Ma from syntectonic granites in the forearc indicate the timing of partial melting and mafic underplating of the prism in response to ridge subduction. The thermal peak in the Damara belt, associated widespread granitic and alkalic plutonism, and hydrothermal activity coincide with the waning stages of tectonism at 530–520 Ma and are interpreted to indicate slab window widening and slab delamination. We suggest that the proposed two-stage thermal evolution of the Damara belt, comprising latest Neoproterozoic ridge subduction and early Cambrian slab delamination, represents a fingerprint of ridge subduction in ancient orogens.
Labels:
Ediacaran,
geology,
namibia,
Neoproterozoic,
orogeny,
precambrian,
Proterozoic,
subduction
Tuesday, April 22, 2014
Complex Feeding Patterns Five Million Years Before The Precambrian–Cambrian Boundary
Trace Fossils with Spreiten from the Late Ediacaran Nama Group, Namibia: Complex Feeding Patterns Five Million Years Before The Precambrian–Cambrian Boundary
Authors:
Macdonald et al
Abstract:
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.
Labels:
animal behavior,
Ediacaran,
namibia,
Neoproterozoic,
precambrian,
trace fossils
Tuesday, October 22, 2013
Interesting Environmental Changes Documented in Namibian Ediacaran NeoProterozoic
Stratigraphy, Palaeontology and Geochemistry of the late Neoproterozoic Aar Member, southwest Namibia; Reflecting environmental controls on Ediacara fossil preservation during the terminal Proterozoic in African Gondwana
Authors:
Hall et al
Abstract:
Common, Ediacaran fossils are well preserved in a Late Neoproterozoic (ca. 545 Ma) shallow marine sequence, described here as the Aar Member of the Dabis Formation (Kuibis Subgroup, Nama Group), near Aus in southwest Namibia. This 31-38 m thick, shale-dominant unit records the transition from fluvial-shallow marine Kliphoek Sandstone to open marine limestone of the Mooifontein Member of the Zaris Formation, deposited on a subsiding continental margin during a major, regional transgression. Thin sandstone beds contain fossils at a number of levels throughout the Aar Member. Concentrations of Pteridinium were mostly transported in flood-derived sheets, while some Ernietta assemblages are preserved close to in-situ. Rangea has also been transported, and is mostly confined to thin sandstone lenses incised into mudstone. Limestone beds, common throughout, include at least two marker horizons that can be followed regionally and show local evidence of storm reworking. Systematic sampling and analyses of limestone reveals enrichment in both 13C and 18O higher in the section, with negative δ13C near the base rising to moderate positive values near the top. The negative-to-positive transition in δ13C values is more pronounced in the east, with all of the lower Aar Member samples consistently depleted in 13C. While this may reflect greater degrees of alteration by meteoric or dewatering fluids, the same carbonates are notably enriched in 18O relative to those at the same stratigraphic position to the west. The overall rise in 13C is attributed to greater proportional burial of organic matter and release of oxygen to surface environments, while the spatial variability is likely the result of a strong surface-to-deep carbon isotopic gradient in seawater. A number of the fossils, especially Rangea, are encrusted with jarosite, an iron-bearing sulphate mineral and common weathering product of pyrite. This observation suggests that preservation of the fossils may have resulted from the rapid encrustation of pyritic on the surface of the organisms as they decomposed and were consumed by sulphate-reducing bacteria within the sandy, near shore sediments. Insofar as pyrite formation requires iron, which is soluble and reactive in anoxic solutions, it is likely that the deeper subtidal environments lacked oxygen. In-situ pyritized forms like Ernietta may have developed the capacity to survive under episodically anoxic or sub-oxic environmental conditions, while Pteridinium and Rangea lived within an oxygenated estuarine or fluvial setting and were transported during storms to anoxic, ferruginous environments where they were exquisitely preserved
Labels:
Ediacaran,
fossils,
geochemistry,
geology,
namibia,
Neoproterozoic,
paleoenvironment,
paleontology,
paleooceans,
Proterozoic
Thursday, March 18, 2010
A Hydrogen Sulfide Upwelling Off Namibia

Hydrogen sulfide erupted along the coast of Namibia in mid-March 2010. Pale-hued waters along the shore hinted at gaseous rumblings as the Moderate Resolution Imaging Spectroradiometer (MODIS) on NASA’s Terra satellite passed overhead and captured this true-color image on March 13, 2010. Although ocean water appears navy blue farther from shore, water along the coast ranges in color from peacock green to off-white. Ocean water wells up in this area along the continental shelf.
The milky surface waters that coincide with gaseous eruptions along Namabia’s coast have a low oxygen content. As reported in a 2009 study, the frequent hydrogen sulfide emissions in this area result form a combination of factors: ocean-current delivery of oxygen-poor water from the north, oxygen-depleting demands of biological and chemical processes in the local water column, and carbon-rich organic sediments under the water column.
Ugh. Theoretically, this was very common during the Permian Extinction. It would be interesting to know how often this happens in our current well mixed oceans.
Labels:
africa,
environment,
namibia,
Permian Extinction,
pictures,
PT Event
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