Table Mountain (table + mountain)

Distribution by Scientific Domains


Selected Abstracts


Genetic population structure of the net-winged midge, Elporia barnardi (Diptera: Blephariceridae) in streams of the south-western Cape, South Africa: implications for dispersal

FRESHWATER BIOLOGY, Issue 1 2003
M. J. Wishart
SUMMARY 1.,The net-winged midges (Diptera: Blephariceridae), with highly specific habitat requirements and specialised morphological adaptations, exhibit high habitat fidelity and a limited potential for dispersal. Given the longitudinal and hierarchical nature of lotic systems, along with the geological structure of catchment units, we hypothesise that populations of net-winged midge should exhibit a high degree of population sub-structuring. 2.,Sequence variation in the cytochrome c oxidase subunit I (COI) region of the mitochondrial DNA (mtDNA) was examined to determine patterns of genetic variation and infer historical and contemporary processes important in the genetic structuring of populations of Elporia barnardi. The DNA variation was examined at sites within streams, between streams in the same range, and between mountain ranges in the south-western Cape of South Africa. 3.,Twenty-five haplotypes, 641 bp in length, were identified from the 93 individuals sampled. A neighbour-joining tree revealed two highly divergent clades (,5%) corresponding to populations from the two mountain ranges. A number of monophyletic groups were identified within each clade, associated with individual catchment units. 4.,The distribution of genetic variation was examined using analysis of molecular variance (amova). This showed most of the variation to be distributed among the two ranges (,80%), with a small percentage (,15%) distributed among streams within each range. Similarly, variation among streams on Table Mountain was primarily distributed among catchment units (86%). A Mantel's test revealed a significant relationship between genetic differentiation and geographical distance, suggesting isolation by distance (P < 0.001). 5.,Levels of sequence divergence between the two major clades, representing the two mountain ranges, are comparable with those of some intra-generic species comparisons. Vicariant events, such as the isolation of the Peninsula mountain chain and Table Mountain, may have been important in the evolution of what is now a highly endemic fauna. 6.,The monophyletic nature of the catchment units suggests that dispersal is confined to the stream environment and that mountain ridges provide effective physical barriers to dispersal of E. barnardi. [source]


Depositional environment of Sirius Group sediments, Table Mountain, Dry Valleys area, Antarctica

GEOGRAFISKA ANNALER SERIES A: PHYSICAL GEOGRAPHY, Issue 1 2002
James R. Goff
Outcrops and cores of the Sirius Group sediments were studied at Table Mountain, Dry Valleys area, Antarctica. These sediments form a surficial veneer at least 9.5 m thick. Three facies , a gravelly sandstone, a sandstone, and a sandy conglomerate , are mapped and described from 13 outcrops and three cores. The gravelly sandstone, constituting 13%of all cored material, is bimodal with matrix-supported clasts comprising 5,33%of the facies. Fabric analysis indicates that it was deposited primarily by lodgment from glacial ice but with minor elements of meltout and flow. The sandstone facies, constituting 77%of all cored material, is a well-sorted, fine- to medium-grained sand, which commonly has laminated bedding. It is predominantly a glaciofluvial deposit but has some glaciolacustrine elements. The sandy conglomerate, constituting 10%of all cored material, is a minor facies. It is massive and clast-supported. It was deposited in a high-energy environment suggestive of subglacial meltwater channels. Sirius Group sediments at Table Mountain are the result of wet-based ice advancing and retreating over waterlain deposits. This is consistent with an advancing ice mass in climatic conditions that were warmer than present. The majority of the sediments were deposited by alpine ice following a similar pathway to the present-day Ferrar Glacier and as such the depositional environment is one that concurs with evidence of a stable East Antarctic Ice Sheet approach. At Table Mountain, the predominantly glaciofluvial and glaciolacustrine facies is inferred to represent a more distal part of the Sirius Group environment than that seen at other outcrops in the Dry Valleys. [source]


Palaeovegetational and palaeoenvironmental trends in the summit of the Guaiquinima massif (Venezuelan Guayana) during the Holocene,

JOURNAL OF QUATERNARY SCIENCE, Issue 2 2005
Valentí Rull
Abstract The summits of the table mountains (tepuis) from the Neotropical Guayana region are remote environments suitable for palaeoecological studies with evolutionary, biogeographical and palaeoclimatic implications. Here, using palynological analyses of two radiocarbon-dated peat bogs from a tepui summit, the Holocene palaeovegetational trends are reconstructed, and related to possible forcing factors. Because of the pristine character of the Guaiquinima summit, the recorded palaeoenvironmental changes are probably due to natural causes, which makes them valuable archives of the natural component of climatic change at a millennial time scale. The sequence begins with pioneer communities or meadows similar to present-day ones, between about 8.4 and 4.5,ky BP. After this date, and until about 2,kyr BP the expansion of gallery forests suggests an increase in precipitation, documented also at regional (Neotropical) level. Between ca. 2,kyr BP and the last century, gallery forests are replaced by forests characteristic of the upper Guaiquinima altitudes, coinciding with a regional phase of reduced moisture. The present-day meadows, established relatively quickly during the last century, substituted the former upland forests. In the locality studied, the main controlling factor of the vegetation during the Holocene seems to have been the moisture balance. In contrast to other tepui summits, there is no clear evidence for changes linked to temperature oscillations. This could be due to the elevation of the site, far from any characteristic ecological boundary, that makes it insensitive to this parameter. Copyright © 2005 John Wiley & Sons, Ltd. [source]