Species-Habitat Associations in a Sri Lankan Dipterocarp Forest

Forest structure and species distribution patterns were examined among eight topographically defined habitats for the 205 species with stems ϵ 1 cm dbh inhabiting a 25-ha plot in the Sinharaja rain forest, Sri Lanka. The habitats were steep spurs, less-steep spurs, steep gullies and less-steep gulli...

Ausführliche Beschreibung

Bibliographische Detailangaben
Veröffentlicht in:Journal of Tropical Ecology. - Cambridge University Press, 1985. - 22(2006), 4, Seite 371-384
1. Verfasser: Gunatilleke, C. V. S. (VerfasserIn)
Weitere Verfasser: Harms, K. E., Ashton, P. M. S., Ashton, P. S.
Format: Online-Aufsatz
Sprache:English
Veröffentlicht: 2006
Zugriff auf das übergeordnete Werk:Journal of Tropical Ecology
Schlagworte:Environmental Heterogeneity Habitat Specialization Rain Forest Sinharaja Forest Dynamics Plot Species-Habitat Associations Sri Lanka Torus Translations Biological sciences Physical sciences
LEADER 01000caa a22002652 4500
001 JST053645839
003 DE-627
005 20240621222524.0
007 cr uuu---uuuuu
008 150324s2006 xx |||||o 00| ||eng c
035 |a (DE-627)JST053645839 
035 |a (JST)4091927 
040 |a DE-627  |b ger  |c DE-627  |e rakwb 
041 |a eng 
100 1 |a Gunatilleke, C. V. S.  |e verfasserin  |4 aut 
245 1 0 |a Species-Habitat Associations in a Sri Lankan Dipterocarp Forest 
264 1 |c 2006 
336 |a Text  |b txt  |2 rdacontent 
337 |a Computermedien  |b c  |2 rdamedia 
338 |a Online-Ressource  |b cr  |2 rdacarrier 
520 |a Forest structure and species distribution patterns were examined among eight topographically defined habitats for the 205 species with stems ϵ 1 cm dbh inhabiting a 25-ha plot in the Sinharaja rain forest, Sri Lanka. The habitats were steep spurs, less-steep spurs, steep gullies and less-steep gullies, all at either lower or upper elevations. Mean stem density was significantly greater on the upper spurs than in the lower, less-steep gullies. Stem density was also higher on spurs than in gullies within each elevation category and in each upper-elevation habitat than in its corresponding lower-elevation habitat. Basal area varied less among habitats, but followed similar trends to stem density. Species richness and Fisher's alpha were lower in the upper-elevation habitats than in the lower-elevation habitats. These differences appeared to be related to the abundances of the dominant species. Of the 125 species subjected to torus-translation tests, 99 species (abundant and less abundant and those in different strata) showed at least one positive or negative association to one or more of the habitats. Species associations were relatively more frequent with the lower-elevation gullies. These and the previous findings on seedling ecophysiology, morphology and anatomy of some of the habitat specialists suggest that edaphic and hydrological variation related to topography, accompanied by canopy disturbances of varying intensity, type and extent along the catenal landscape, plays a major role in habitat partitioning in this forest. 
540 |a Copyright 2006 Cambridge University Press 
650 4 |a Environmental Heterogeneity 
650 4 |a Habitat Specialization 
650 4 |a Rain Forest 
650 4 |a Sinharaja Forest Dynamics Plot 
650 4 |a Species-Habitat Associations 
650 4 |a Sri Lanka 
650 4 |a Torus Translations 
650 4 |a Biological sciences  |x Biology  |x Botany  |x Plant ecology  |x Forest ecology  |x Forest ecosystems  |x Forest habitats 
650 4 |a Biological sciences  |x Biology  |x Botany  |x Plant ecology  |x Forest ecology 
650 4 |a Biological sciences  |x Ecology  |x Population ecology  |x Synecology  |x Habitats 
650 4 |a Biological sciences  |x Ecology  |x Population ecology  |x Synecology  |x Biocenosis  |x Plant communities  |x Forests  |x Rain forests  |x Tropical rain forests 
650 4 |a Biological sciences  |x Ecology  |x Wildlife ecology  |x Wildlife habitats 
650 4 |a Physical sciences  |x Earth sciences  |x Geography  |x Geomorphology  |x Topography  |x Topographical elevation 
650 4 |a Biological sciences  |x Biology  |x Botany  |x Dendrology  |x Trees 
650 4 |a Biological sciences  |x Ecology  |x Population ecology  |x Synecology  |x Biocenosis  |x Plant communities  |x Forests  |x Tropical forests 
650 4 |a Biological sciences  |x Biology  |x Biological taxonomies  |x Species 
650 4 |a Biological sciences  |x Biology  |x Botany  |x Plant ecology  |x Vegetation  |x Vegetation structure  |x Plant strata  |x Vegetation canopies  |x Forest canopy 
655 4 |a research-article 
700 1 |a Harms, K. E.  |e verfasserin  |4 aut 
700 1 |a Ashton, P. M. S.  |e verfasserin  |4 aut 
700 1 |a Ashton, P. S.  |e verfasserin  |4 aut 
773 0 8 |i Enthalten in  |t Journal of Tropical Ecology  |d Cambridge University Press, 1985  |g 22(2006), 4, Seite 371-384  |w (DE-627)266015972  |w (DE-600)1466679-0  |x 14697831  |7 nnns 
773 1 8 |g volume:22  |g year:2006  |g number:4  |g pages:371-384 
856 4 0 |u https://www.jstor.org/stable/4091927  |3 Volltext 
912 |a GBV_USEFLAG_A 
912 |a SYSFLAG_A 
912 |a GBV_JST 
912 |a GBV_ILN_11 
912 |a GBV_ILN_20 
912 |a GBV_ILN_22 
912 |a GBV_ILN_24 
912 |a GBV_ILN_31 
912 |a GBV_ILN_39 
912 |a GBV_ILN_40 
912 |a GBV_ILN_60 
912 |a GBV_ILN_62 
912 |a GBV_ILN_63 
912 |a GBV_ILN_69 
912 |a GBV_ILN_70 
912 |a GBV_ILN_73 
912 |a GBV_ILN_74 
912 |a GBV_ILN_90 
912 |a GBV_ILN_100 
912 |a GBV_ILN_101 
912 |a GBV_ILN_105 
912 |a GBV_ILN_110 
912 |a GBV_ILN_120 
912 |a GBV_ILN_161 
912 |a GBV_ILN_285 
912 |a GBV_ILN_293 
912 |a GBV_ILN_374 
912 |a GBV_ILN_602 
912 |a GBV_ILN_636 
912 |a GBV_ILN_702 
912 |a GBV_ILN_2001 
912 |a GBV_ILN_2003 
912 |a GBV_ILN_2005 
912 |a GBV_ILN_2006 
912 |a GBV_ILN_2007 
912 |a GBV_ILN_2008 
912 |a GBV_ILN_2009 
912 |a GBV_ILN_2010 
912 |a GBV_ILN_2011 
912 |a GBV_ILN_2014 
912 |a GBV_ILN_2015 
912 |a GBV_ILN_2018 
912 |a GBV_ILN_2020 
912 |a GBV_ILN_2021 
912 |a GBV_ILN_2026 
912 |a GBV_ILN_2027 
912 |a GBV_ILN_2044 
912 |a GBV_ILN_2050 
912 |a GBV_ILN_2056 
912 |a GBV_ILN_2057 
912 |a GBV_ILN_2061 
912 |a GBV_ILN_2088 
912 |a GBV_ILN_2093 
912 |a GBV_ILN_2107 
912 |a GBV_ILN_2110 
912 |a GBV_ILN_2190 
912 |a GBV_ILN_2336 
912 |a GBV_ILN_2470 
912 |a GBV_ILN_2522 
912 |a GBV_ILN_2548 
912 |a GBV_ILN_2939 
912 |a GBV_ILN_2942 
912 |a GBV_ILN_2946 
912 |a GBV_ILN_2949 
912 |a GBV_ILN_2951 
912 |a GBV_ILN_4012 
912 |a GBV_ILN_4035 
912 |a GBV_ILN_4037 
912 |a GBV_ILN_4046 
912 |a GBV_ILN_4112 
912 |a GBV_ILN_4125 
912 |a GBV_ILN_4126 
912 |a GBV_ILN_4242 
912 |a GBV_ILN_4246 
912 |a GBV_ILN_4251 
912 |a GBV_ILN_4305 
912 |a GBV_ILN_4306 
912 |a GBV_ILN_4307 
912 |a GBV_ILN_4313 
912 |a GBV_ILN_4322 
912 |a GBV_ILN_4323 
912 |a GBV_ILN_4324 
912 |a GBV_ILN_4325 
912 |a GBV_ILN_4335 
912 |a GBV_ILN_4346 
912 |a GBV_ILN_4393 
912 |a GBV_ILN_4700 
951 |a AR 
952 |d 22  |j 2006  |e 4  |h 371-384