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  • 1
    Publication Date: 2014-04-30
    Description: Speciation generally involves a three-step process--range expansion, range fragmentation and the development of reproductive isolation between spatially separated populations. Speciation relies on cycling through these three steps and each may limit the rate at which new species form. We estimate phylogenetic relationships among all Himalayan songbirds to ask whether the development of reproductive isolation and ecological competition, both factors that limit range expansions, set an ultimate limit on speciation. Based on a phylogeny for all 358 species distributed along the eastern elevational gradient, here we show that body size and shape differences evolved early in the radiation, with the elevational band occupied by a species evolving later. These results are consistent with competition for niche space limiting species accumulation. Even the elevation dimension seems to be approaching ecological saturation, because the closest relatives both inside the assemblage and elsewhere in the Himalayas are on average separated by more than five million years, which is longer than it generally takes for reproductive isolation to be completed; also, elevational distributions are well explained by resource availability, notably the abundance of arthropods, and not by differences in diversification rates in different elevational zones. Our results imply that speciation rate is ultimately set by niche filling (that is, ecological competition for resources), rather than by the rate of acquisition of reproductive isolation.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Price, Trevor D -- Hooper, Daniel M -- Buchanan, Caitlyn D -- Johansson, Ulf S -- Tietze, D Thomas -- Alstrom, Per -- Olsson, Urban -- Ghosh-Harihar, Mousumi -- Ishtiaq, Farah -- Gupta, Sandeep K -- Martens, Jochen -- Harr, Bettina -- Singh, Pratap -- Mohan, Dhananjai -- England -- Nature. 2014 May 8;509(7499):222-5. doi: 10.1038/nature13272. Epub 2014 Apr 30.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Ecology and Evolution, University of Chicago, Chicago, Illinois 60637, USA. ; 1] Department of Ecology and Evolution, University of Chicago, Chicago, Illinois 60637, USA [2] Department of Zoology, Swedish Museum of Natural History, 10405 Stockholm, Sweden. ; 1] Department of Ecology and Evolution, University of Chicago, Chicago, Illinois 60637, USA [2] Institute of Pharmacy and Molecular Biotechnology, University of Heidelberg, Im Neuenheimer Feld 364, 69120 Heidelberg, Germany. ; 1] Key Laboratory of Zoological Systematics and Evolution, Institute of Zoology, Chinese Academy of Sciences, 1 Beichen West Road, Chaoyang District, Beijing 100101, China [2] Swedish Species Information Centre, Swedish University of Agricultural Sciences, Box 7007, 75007 Uppsala, Sweden. ; Systematics and Biodiversity, Department of Biology and Environmental Sciences, University of Gothenburg, 40530 Gothenburg, Sweden. ; Wildlife Institute of India, PO Box 18, Chandrabani, Dehradun 248001, India. ; Institute of Zoology, Johannes Gutenberg University, Mainz 55099, Germany. ; Max Planck Institute for Evolutionary Biology, August Thienemannstrasse 2, 24306 Plon, Germany.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/24776798" target="_blank"〉PubMed〈/a〉
    Keywords: *Altitude ; Animals ; Body Size ; China ; *Ecosystem ; *Genetic Speciation ; India ; Phylogeny ; Reproduction ; Songbirds/anatomy & histology/*classification/*physiology ; Tibet
    Print ISSN: 0028-0836
    Electronic ISSN: 1476-4687
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
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  • 2
    Publication Date: 2015-11-21
    Description: The DNA-binding protein PRDM9 has a critical role in specifying meiotic recombination hotspots in mice and apes, but it appears to be absent from other vertebrate species, including birds. To study the evolution and determinants of recombination in species lacking the gene that encodes PRDM9, we inferred fine-scale genetic maps from population resequencing data for two bird species: the zebra finch, Taeniopygia guttata, and the long-tailed finch, Poephila acuticauda. We found that both species have recombination hotspots, which are enriched near functional genomic elements. Unlike in mice and apes, most hotspots are shared between the two species, and their conservation seems to extend over tens of millions of years. These observations suggest that in the absence of PRDM9, recombination targets functional features that both enable access to the genome and constrain its evolution.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Singhal, Sonal -- Leffler, Ellen M -- Sannareddy, Keerthi -- Turner, Isaac -- Venn, Oliver -- Hooper, Daniel M -- Strand, Alva I -- Li, Qiye -- Raney, Brian -- Balakrishnan, Christopher N -- Griffith, Simon C -- McVean, Gil -- Przeworski, Molly -- 086786/Z/08/Z/Wellcome Trust/United Kingdom -- 090532/Z/09/Z/Wellcome Trust/United Kingdom -- 100956/Wellcome Trust/United Kingdom -- Howard Hughes Medical Institute/ -- New York, N.Y. -- Science. 2015 Nov 20;350(6263):928-32. doi: 10.1126/science.aad0843.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Biological Sciences, Columbia University, New York, NY 10027, USA. Department of Systems Biology, Columbia University, New York, NY 10032, USA. sonal.singhal1@gmail.com molly.przew@gmail.com. ; Department of Human Genetics, University of Chicago, Chicago, IL 60637, USA. Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford OX3 7BN, UK. ; Department of Human Genetics, University of Chicago, Chicago, IL 60637, USA. ; Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford OX3 7BN, UK. ; Committee on Evolutionary Biology, University of Chicago, Chicago, IL 60637, USA. ; Department of Biological Sciences, Columbia University, New York, NY 10027, USA. ; China National Genebank, BGI-Shenzhen, Shenzhen 518083, China. ; Center for Biomolecular Science and Engineering, University of California-Santa Cruz, Santa Cruz, CA 95064, USA. ; Department of Biology, East Carolina University, Greenville, NC 27858, USA. ; Department of Biological Sciences, Macquarie University, Sydney, NSW 2109, Australia.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/26586757" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Chromosome Mapping ; *Evolution, Molecular ; Finches/*genetics ; *Gene Expression Regulation ; Genome ; *Recombination, Genetic ; Repressor Proteins/*genetics ; Species Specificity
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 3
    Publication Date: 1991-11-01
    Print ISSN: 0143-1161
    Electronic ISSN: 1366-5901
    Topics: Architecture, Civil Engineering, Surveying , Geography
    Published by Taylor & Francis
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  • 4
    Publication Date: 2019-07-12
    Description: Seasonal reflectance variations in semigrid environments provide a means of assessing vegetation health and density as well as monitoring landform processes. Multitemporal Landsat Thematic Mapper scenes with field measurements are used to map geomorphology and vegetation density in a stabilized dune environment and to measure seasonal reflectance changes for a series of ten geomorphological and vegetation units on the Kalahari-age linear dunes. Units were chosen based on differences in landform and proportion of trees, forbs and bare soil. Reflectance curves and normalized-difference vegetation indices (NDVI) show that dune crests have the strongest seasonal variability in color and brightness. The geomorphological link with reflectance and NDVI values are linked to biomass production and zoning of vegetation with slope, drainage and subtle soil differences.
    Keywords: EARTH RESOURCES AND REMOTE SENSING
    Type: International Journal of Remote Sensing (ISSN 0143-1161); 12; 2321-234
    Format: text
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