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Drastic Effects (drastic + effects)
Selected AbstractsExploring the diversity of bacterial communities in sediments of urban mangrove forestsFEMS MICROBIOLOGY ECOLOGY, Issue 1 2008Newton C. Marcial Gomes Abstract Municipal sewage, urban runoff and accidental oil spills are common sources of pollutants in urban mangrove forests and may have drastic effects on the microbial communities inhabiting the sediment. However, studies on microbial communities in the sediment of urban mangroves are largely lacking. In this study, we explored the diversity of bacterial communities in the sediment of three urban mangroves located in Guanabara Bay (Rio de Janeiro, Brazil). Analysis of sediment samples by means of denaturing gradient gel electrophoresis (DGGE) of 16S rRNA gene fragments suggested that the overall bacterial diversity was not significantly affected by the different levels of hydrocarbon pollution at each sampling site. However, DGGE and sequence analyses provided evidences that each mangrove sediment displayed a specific structure bacterial community. Although primer sets for Pseudomonas, alphaproteobacterial and actinobacterial groups also amplified ribotypes belonging to taxa not intended to be enriched, sequence analyses of dominant DGGE bands revealed ribotypes related to Alteromonadales, Burkholderiales, Pseudomonadales, Rhodobacterales and Rhodocyclales. Members of these groups were often shown to be involved in aerobic or anaerobic degradation of hydrocarbon pollutants. Many of these sequences were only detected in the sampling sites with high levels of anthropogenic inputs of hydrocarbons. Many dominant DGGE ribotypes showed low levels of sequence identity to known sequences, indicating a large untapped bacterial diversity in mangrove ecosystems. [source] Genetic diversity and Wolbachia infection of the Drosophila parasitoid Leptopilina clavipes in western EuropeMOLECULAR ECOLOGY, Issue 5 2004Bart A. Pannebakker Abstract Wolbachia are maternally transmitted bacteria that alter their arthropod hosts' reproduction in various ways, including parthenogenesis induction (PI). Wolbachia -induced parthenogenesis can have drastic effects on the genetic structure of its host because it potentially reduces populations to clones without genetic exchange. However, Wolbachia -induced parthenogenesis does not inevitably result in a reduction of genetic variation of infected populations vs. uninfected populations, because the parthenogenetic populations are initially derived from uninfected populations and can thus show similar genetic variation. Here we investigate these issues in infected and uninfected populations of the Drosophila parasitoid Leptopilina clavipes in western Europe. Wasps from 19 sites in the Netherlands, France and northern Spain were screened for Wolbachia and analysed using amplified fragment length polymorphism (AFLP) markers. All the populations from the Netherlands and mid-France were infected with the same two strains of Wolbachia, whereas populations from the Pyrenees were not infected. The infected and uninfected populations show identical levels of genetic variation, but have clearly diverged genetically, indicating the presence of a barrier that prevents gene flow. Within the infected wasps two distinct genotypes were found at multiple localities, indicating the coexistence of multiple clones. The conditions promoting clonal coexistence in L. clavipes are discussed. [source] The effects of GaAs interval layer on GaNAs/GaAs superlattice structure grown by RF-MBE using modulated N radical beam sequencePHYSICA STATUS SOLIDI (C) - CURRENT TOPICS IN SOLID STATE PHYSICS, Issue 9 2008Kensuke Fujii Abstract We have investigated the effects of GaAs interval layers on the structure of GaNAs/GaAs superlattices (SLs) grown by radio-frequency molecular beam epitaxy. As the results of x-ray diffraction, it is found that periodic structure of GaNAs/GaAs SL is better in the case of thicker GaAs layer than that of thin GaAs layer, whereas the GaNAs layer thickness is constant of 10 ML. Transmission electron microscope (TEM) studies of SL samples clearly demonstrate the drastic effects of GaAs layer thickness on the GaNAs/GaAs SL structures. High resolution TEM study of the sample with a thin AlAs layer inserted between GaNAs and GaAs, for improved contrast, reveals existence of the roughening process during GaNAs layer growth and the smoothing process during GaAs layer growth. (© 2008 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim) [source] Seed plants of Fiji: an ecological analysisBIOLOGICAL JOURNAL OF THE LINNEAN SOCIETY, Issue 3 2006MICHAEL HEADS An annotated list of indigenous Fijian seed plant genera is presented and comprises 484 genera and 1315 species in 137 families. The relative diversity of the largest families and genera in Fiji is indicated and compared with floras in New Caledonia and the Upper Watut Valley, Papua New Guinea. Differences and similarities appear to be due to biogeographical/phylogenetic factors rather than ecological differences or means of dispersal. Generic diversity for the seed plants as a whole is greatest between 0,100 m and decreases monotonically with altitude. However, in the largest family, Orchidaceae, maximum diversity occurs between 200,400 m. Fifty percent of the families are recorded from shore habitat. Twenty-seven percent of the families and 80 species occur in or around mangrove, where the most diverse families are Orchidaceae, Rubiaceae, and the legumes. Some of the mangrove-associate species are pantropical or Indo-Pacific but most are locally or regionally endemic. Fifty-six percent of the Fijian families are recorded on limestone. Twenty-nine species are restricted to limestone and 12 species usually occur on limestone. The importance of calcium in reducing the effects of salinity is emphasized and 39 species are recorded from both mangrove and limestone. A plagiotropic habit occurs in 38 species which occur on limestone or around beaches, and 20 of these are Pacific endemics. Genera restricted to higher altitudes include many present elsewhere in Melanesia but absent from Australia despite suitable habitat there, again indicating the importance of biogeographical and historical factors. Altitudinal anomalies in Fiji taxa are cited and include 7 anomalously high records from northern Viti Levu, a site of major uplift, and 22 anomalously low altitudinal records in the Lau Group, a site of subsidence. It is suggested that the Fijian flora has not been derived from immigrants from Asia, but has evolved more or less in situ. Taxa would have survived as metapopulations on the individually ephemeral volcanic islands always found at oceanic subduction zones and hot spots, and the atolls which characterize areas of subsidence. The complex geology of Fiji is determined by its position between two subduction zones of opposite polarity, the Vanuatu and Tonga Trenches, in what is currently a region of transform faulting. The large islands comprise fragments of island arcs that have amalgamated and welded together. There has been considerable uplift as well as subsidence in the islands and it is suggested that both these processes have had drastic effects on the altitudinal range of the taxa. Limestone and mangrove floras could have provided a widespread, diverse ancestral species pool from which freshwater swamp forest, lowland rainforest, dry forest, secondary forest, thickets, and montane forest have been derived during phases of uplift. © 2006 The Linnean Society of London, Biological Journal of the Linnean Society, 2006, 89, 407,431. [source] | ||||||||||