|
|
|
|
LEADER |
01000caa a22002652 4500 |
001 |
JST066881773 |
003 |
DE-627 |
005 |
20240622150215.0 |
007 |
cr uuu---uuuuu |
008 |
150325s2007 xx |||||o 00| ||eng c |
035 |
|
|
|a (DE-627)JST066881773
|
035 |
|
|
|a (JST)40212961
|
040 |
|
|
|a DE-627
|b ger
|c DE-627
|e rakwb
|
041 |
|
|
|a eng
|
100 |
1 |
|
|a Queenborough, Simon A.
|e verfasserin
|4 aut
|
245 |
1 |
0 |
|a Habitat Niche Partitioning by 16 Species of Myristicaceae in Amazonian Ecuador
|
264 |
|
1 |
|c 2007
|
336 |
|
|
|a Text
|b txt
|2 rdacontent
|
337 |
|
|
|a Computermedien
|b c
|2 rdamedia
|
338 |
|
|
|a Online-Ressource
|b cr
|2 rdacarrier
|
520 |
|
|
|a The distribution and spatial pattern of plants in tropical forests have important implications for how species interact with each other and their environments. In this article we use a large-scale permanent census plot to address if the coexistence of 16 co-occurring species of Myristicaceae is aided by topographic and light gradient niche partitioning. We used a second order spatial pattern analysis based on Ripley's K function to describe species' distributions and associations among species, and a torus translation procedure to test for associations with three topographically defined habitats. A majority of species displayed spatial aggregation and over half had one or more significant habitat associations. Four species were associated with the ridge habitat, four species with slope habitat, and two with valley habitat. Seven other species showed no habitat association. Within each habitat group, species exhibited a variety of distributions in relation to light availability. However, habitat associations were largely unexplained by differential rates of mortality, growth or recruitment over a 5-year interval. We conclude that although in principle partitioning of the topographic and light environments may double or treble the number of species able to coexist, there is no evidence that partitioning of physical habitats can explain the coexistence of all 16 of these closely related species.
|
650 |
|
4 |
|a Coexistence
|
650 |
|
4 |
|a Lowland tropical rain forest
|
650 |
|
4 |
|a Species diversity
|
650 |
|
4 |
|a Yasuní
|
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 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 Biology
|x Botany
|x Dendrology
|x Trees
|
650 |
|
4 |
|a Physical sciences
|x Earth sciences
|x Geography
|x Geomorphology
|x Topography
|x Sloping terrain
|
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 Botany
|x Dendrology
|x Trees
|x Forest trees
|
650 |
|
4 |
|a Social sciences
|x Population studies
|x Mortality
|
650 |
|
4 |
|a Biological sciences
|x Ecology
|x Animal ecology
|x Habitat preferences
|
650 |
|
4 |
|a Biological sciences
|x Biology
|x Botany
|x Plant ecology
|x Forest ecology
|
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 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 Biology
|x Botany
|x Dendrology
|x Trees
|
650 |
|
4 |
|a Physical sciences
|x Earth sciences
|x Geography
|x Geomorphology
|x Topography
|x Sloping terrain
|
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 Botany
|x Dendrology
|x Trees
|x Forest trees
|
650 |
|
4 |
|a Social sciences
|x Population studies
|x Mortality
|
650 |
|
4 |
|a Biological sciences
|x Ecology
|x Animal ecology
|x Habitat preferences
|
650 |
|
4 |
|a Biological sciences
|x Biology
|x Botany
|x Plant ecology
|x Forest ecology
|
655 |
|
4 |
|a research-article
|
700 |
1 |
|
|a Burslem, David F. R. P.
|e verfasserin
|4 aut
|
700 |
1 |
|
|a Garwood, Nancy C.
|e verfasserin
|4 aut
|
700 |
1 |
|
|a Valencia, Renato
|e verfasserin
|4 aut
|
773 |
0 |
8 |
|i Enthalten in
|t Plant Ecology
|d Springer Science + Business Media
|g 192(2007), 2, Seite 193-207
|w (DE-627)271177578
|w (DE-600)1479167-5
|x 15735052
|7 nnns
|
773 |
1 |
8 |
|g volume:192
|g year:2007
|g number:2
|g pages:193-207
|
856 |
4 |
0 |
|u https://www.jstor.org/stable/40212961
|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_23
|
912 |
|
|
|a GBV_ILN_24
|
912 |
|
|
|a GBV_ILN_31
|
912 |
|
|
|a GBV_ILN_32
|
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_65
|
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_95
|
912 |
|
|
|a GBV_ILN_100
|
912 |
|
|
|a GBV_ILN_105
|
912 |
|
|
|a GBV_ILN_110
|
912 |
|
|
|a GBV_ILN_120
|
912 |
|
|
|a GBV_ILN_138
|
912 |
|
|
|a GBV_ILN_150
|
912 |
|
|
|a GBV_ILN_151
|
912 |
|
|
|a GBV_ILN_152
|
912 |
|
|
|a GBV_ILN_161
|
912 |
|
|
|a GBV_ILN_170
|
912 |
|
|
|a GBV_ILN_171
|
912 |
|
|
|a GBV_ILN_187
|
912 |
|
|
|a GBV_ILN_213
|
912 |
|
|
|a GBV_ILN_224
|
912 |
|
|
|a GBV_ILN_230
|
912 |
|
|
|a GBV_ILN_250
|
912 |
|
|
|a GBV_ILN_281
|
912 |
|
|
|a GBV_ILN_285
|
912 |
|
|
|a GBV_ILN_293
|
912 |
|
|
|a GBV_ILN_370
|
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_2004
|
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_2025
|
912 |
|
|
|a GBV_ILN_2026
|
912 |
|
|
|a GBV_ILN_2027
|
912 |
|
|
|a GBV_ILN_2031
|
912 |
|
|
|a GBV_ILN_2034
|
912 |
|
|
|a GBV_ILN_2037
|
912 |
|
|
|a GBV_ILN_2038
|
912 |
|
|
|a GBV_ILN_2039
|
912 |
|
|
|a GBV_ILN_2044
|
912 |
|
|
|a GBV_ILN_2048
|
912 |
|
|
|a GBV_ILN_2049
|
912 |
|
|
|a GBV_ILN_2050
|
912 |
|
|
|a GBV_ILN_2055
|
912 |
|
|
|a GBV_ILN_2057
|
912 |
|
|
|a GBV_ILN_2059
|
912 |
|
|
|a GBV_ILN_2061
|
912 |
|
|
|a GBV_ILN_2064
|
912 |
|
|
|a GBV_ILN_2065
|
912 |
|
|
|a GBV_ILN_2068
|
912 |
|
|
|a GBV_ILN_2070
|
912 |
|
|
|a GBV_ILN_2086
|
912 |
|
|
|a GBV_ILN_2088
|
912 |
|
|
|a GBV_ILN_2093
|
912 |
|
|
|a GBV_ILN_2106
|
912 |
|
|
|a GBV_ILN_2107
|
912 |
|
|
|a GBV_ILN_2108
|
912 |
|
|
|a GBV_ILN_2110
|
912 |
|
|
|a GBV_ILN_2111
|
912 |
|
|
|a GBV_ILN_2112
|
912 |
|
|
|a GBV_ILN_2113
|
912 |
|
|
|a GBV_ILN_2116
|
912 |
|
|
|a GBV_ILN_2118
|
912 |
|
|
|a GBV_ILN_2119
|
912 |
|
|
|a GBV_ILN_2122
|
912 |
|
|
|a GBV_ILN_2129
|
912 |
|
|
|a GBV_ILN_2143
|
912 |
|
|
|a GBV_ILN_2144
|
912 |
|
|
|a GBV_ILN_2147
|
912 |
|
|
|a GBV_ILN_2148
|
912 |
|
|
|a GBV_ILN_2152
|
912 |
|
|
|a GBV_ILN_2153
|
912 |
|
|
|a GBV_ILN_2188
|
912 |
|
|
|a GBV_ILN_2190
|
912 |
|
|
|a GBV_ILN_2232
|
912 |
|
|
|a GBV_ILN_2336
|
912 |
|
|
|a GBV_ILN_2446
|
912 |
|
|
|a GBV_ILN_2470
|
912 |
|
|
|a GBV_ILN_2472
|
912 |
|
|
|a GBV_ILN_2507
|
912 |
|
|
|a GBV_ILN_2522
|
912 |
|
|
|a GBV_ILN_2548
|
912 |
|
|
|a GBV_ILN_2939
|
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_4249
|
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_4326
|
912 |
|
|
|a GBV_ILN_4333
|
912 |
|
|
|a GBV_ILN_4334
|
912 |
|
|
|a GBV_ILN_4335
|
912 |
|
|
|a GBV_ILN_4336
|
912 |
|
|
|a GBV_ILN_4338
|
912 |
|
|
|a GBV_ILN_4346
|
912 |
|
|
|a GBV_ILN_4393
|
912 |
|
|
|a GBV_ILN_4700
|
951 |
|
|
|a AR
|
952 |
|
|
|d 192
|j 2007
|e 2
|h 193-207
|