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1 s to restore ecosystem functions rather than species diversity.
2 nsional trait constraints should exhibit low species diversity.
3 adaptation, as well as the quantification of species diversity.
4 ly weaker local NDD, while promoting overall species diversity.
5 structure, including population density and species diversity.
6 -associated STs and 27 representative of the species diversity.
7 no overall changes in relative abundance or species diversity.
8 in the effects of intraspecific variation on species diversity.
9 l planning to protect both food security and species diversity.
10 dom, both in terms of individual numbers and species diversity.
11 ts that are viable and thereby also to lower species diversity.
12 rome oxidase I) revealed significant cryptic species diversity.
13 positive relationship between total dose and species diversity.
14 processes contributing to the maintenance of species diversity.
15 many explanations for regional gradients in species diversity.
16 able and uncertain, particularly in terms of species diversity.
17 r three forest types were unaffected by tree species diversity.
18 ion front creates regions of low genetic and species diversity.
19 types across Europe along a gradient of tree species diversity.
20 CO2 at the end of the experiment, but not by species diversity.
21 signaling and gene expression contributes to species diversity.
22 tance' of taxonomic (lineage) composition or species diversity.
23 .7-5.8 times) associated with an increase in species diversity.
24 s and that this approach also conserves wild-species diversity.
25 eational visits, urban green space, and wild-species diversity.
26 can differ in their contribution to overall species diversity.
27 because parasites represent at least half of species diversity.
28 HI, challenge current views on the origin of species diversity.
29 minant of production, food-chain length, and species diversity.
30 with competition to both enhance and reduce species diversity.
31 significantly increase the estimate of total species diversity.
32 n architectures are specific and account for species diversity.
33 ted to local water availability than overall species diversity.
34 ferences have a critical role in stabilizing species diversity.
35 explanation for the latitudinal gradient in species diversity.
36 evel of grazing often results in the highest species diversity.
37 re; here, we focus on the global recovery of species diversity.
38 rates of origination and broadly with total species diversity.
39 ks between ecology and evolution to maintain species diversity.
40 ncreased as the climate warmed regardless of species diversity.
41 ies in Arkansas were tested to determine the species diversity.
42 t of the canon explaining the maintenance of species diversity.
43 ginine-treated biofilms as well as increased species diversity.
44 of 46-51% for organism abundance, 27-33% for species diversity, 32-42% for carbon cycling and 31-41%
45 how local agro-pastoralists perceive forage species diversity, abundance trends, habitat distributio
46 seedlings and saplings and changes in local species diversity across a soil-resource gradient for 38
47 mbitious study to date on the differences in species diversity across clades in the tree of life.
49 which this mechanism can explain patterns of species diversity across environmental gradients is larg
51 ctions that contribute to the maintenance of species diversity across temperate and tropical communit
52 less to do with the tremendous variation in species diversity across the evolutionary tree of life t
54 tioning field experiment to date to test how species diversity affects the ability of grassland ecosy
55 oss Java, indicating that regions of highest species diversity afford the highest potential to discov
58 at asynchrony across species--much more than species diversity alone--is the main driver of variation
59 more, the opposite trend in the AGB and tree species diversity along the soil fertility gradient led
60 find that most conservation plans targeting species diversity also represent phylogenetic and functi
61 e of this clock is conserved among different species, diversity also exists, especially in terms of t
62 xtinction and, hence, explain differences in species diversity among clades is a major goal of evolut
63 have been a widespread mechanism generating species diversity amongst dinosaurs, and perhaps beyond.
65 s showed a considerable recovery in terms of species diversity and abundance in 3 months and full rec
68 ogether increased community biomass, reduced species diversity and altered community composition.
69 f barley (Hordeum vulgare) genotype and weed species diversity and assessed their relative biodiversi
71 ean is known to be a region of high deep-sea species diversity and centre of origin for the global de
72 heories have been frequently used to explain species diversity and composition in local communities b
73 and livestock assemblages (both in terms of species diversity and composition) has important implica
74 loss of functioning if high-levels of local species diversity and compositional variation across loc
76 esented three phyla with different ranges of species diversity and different number of genomes includ
77 h of ROV footage to investigate patterns of species diversity and document the presence of a range o
78 ction of conifers by pushing their remaining species diversity and dominance out of the warm tropics.
82 is an important mechanism that can maintain species diversity and explain patterns of tree-species r
83 d a larger predictive power for the ABP than species diversity and FDQ, indicating a primary dependen
84 phylogenies are the basis for understanding species diversity and for linking changes in rates of di
85 d not detect a unimodal relationship between species diversity and forest disturbance expected under
86 a unique perspective to current theories of species diversity and has important implications for bio
88 al plant communities exhibit relatively high species diversity and many competitive species are ubiqu
89 till conferred distinct effects on bacterial species diversity and microbiota stability largely in a
92 akers, the lack of advanced understanding of species diversity and of a full survey of any single hab
93 ients and are commonly characterized by high species diversity and primary productivity, which in tur
94 c Ocean basin to show that changes in global species diversity and rates of extinction among plankton
96 and no significant changes were found in the species diversity and richness for any bacterial taxa am
97 , and that such specialization could promote species diversity and seed dispersal in plant communitie
98 s may accelerate the loss of coral coverage, species diversity and structural complexity within subtr
99 ads to recovery of the intestinal microbiota species diversity and suppresses C. difficile levels, al
102 tor species had indirect negative effects on species diversity and total cover of primary producers.
106 32 years to compare seagrass percent cover, species diversity, and community structure in restored a
107 05,634 species, equating to 30% of all plant species diversity, and conserve over 41% of known threat
108 y randomly assembling communities of varying species diversity, and ecosystem functions are measured.
110 te large differences in abiotic environment, species diversity, and taxonomic and functional composit
113 ity results provide additional evidence that species diversity arises without specific physical barri
114 stems, with consequences for the efficacy of species diversity as a buffer against environmental chan
115 al change studies have identified changes in species diversity as a major mechanism regulating tempor
116 o a small number of organisms, instead using species diversity as an opportunity to practice translat
118 ifferent effects of barley genotype and weed species diversity as the consequence of small vs large t
121 we report the effects of organic farming on species diversity at the field, farm and regional levels
122 the Guangzhou retail market and compare the species diversity between the Guangzhou and Hong Kong sh
123 temperatures influence ecosystems, sea ice, species diversity, biogeochemical cycling, seafloor meth
124 cal gradient in structure of a generally low species diversity bioluminescent community at shallower
126 le species diversity and the bulk population species diversity both increased with primary traffic em
127 driving not just whole-island differences in species diversity, but also local community assembly.
128 emporal stability is not influenced by plant species diversity, but is largely determined by the temp
129 l biomass significantly increases with plant species diversity, but it remains unclear whether plant
130 These results imply direct limitation of species diversity by climatic stress and more rapid (co-
131 matic reduction in the intestinal microbiota species diversity, C. difficile overgrowth, and excretio
132 ersity, but it remains unclear whether plant species diversity can also stabilize soil microbial biom
136 xplosion was followed by a reduction of tree species diversity, changing forest composition, altering
137 red gut microbiota suggested that microbiome species diversity correlated with host reactive oxygen s
143 on of these processes to the accumulation of species diversity depends on the area and isolation of t
144 nservation priority regions identified using species diversity differ from those based on phylogeneti
145 Managing forest ecosystems for high tree species diversity does not necessarily assure improved a
148 including: the seasonal variation in overall species diversity due to migration; the contribution of
149 radictory results that were a consequence of species diversity due to mixed infections or minor conta
150 sults provide new insight into genotypic and species diversity effects in plant-neighbour interaction
151 independently examine symbiont genotypic and species diversity found within and between colonies of H
152 t long-term study of fruit-feeding nymphalid species diversity from Central America and provide a uni
154 been observed between sexual dimorphism and species diversity, from positive to negative and nonsign
155 ance tolerance across the competing species, species diversity generally declined with disturbance.
159 ists exhibited extensive knowledge on forage species diversity, habitat types, abundance trends and e
162 relationship between disturbance regimes and species diversity has been of central interest to ecolog
163 Whether hybridization generates or erodes species diversity has long been debated, but to date mos
164 e maintained throughout mammalian evolution, species diversity has precluded direct analysis of human
167 w of both ubiquitous vertebrate features and species diversity, highlighting important nonapeptide ef
169 southwest China (MSC) harbor extremely high species diversity; however, the mechanism behind this di
170 not correlate closely with regions with high species diversity, human population density, or agricult
171 cation dynamics and spatial distributions of species diversity illustrates the benefits of an inclusi
172 cause the biosphere is highly heterogeneous, species diversity impacts are typically assessed at loca
173 le spatial and temporal partitions to assess species diversity in a Costa Rican rainforest butterfly
174 ted filamentous bacteria, and an increase in species diversity in Ahr(-/-) mice following genotypic s
176 s a clear example of the importance of lipid species diversity in biological membranes and importantl
179 namics is necessary for explaining trait and species diversity in communities, even in communities wi
180 wledge of climate-driven directional loss of species diversity in ecological communities in a natural
181 d evolution suggests that the maintenance of species diversity in ecological communities may be influ
182 Among the local processes that determine species diversity in ecological communities, fluctuation
183 rneo and Amazonia may each contain more tree species diversity in half a square kilometre than do all
189 alysis revealed substantial inter- and intra-species diversity in pathways that likely influence an i
192 those clades that have a large proportion of species diversity in rainforests are significantly more
193 of lineages, but the large majority of plant species diversity in rainforests is recent, suggesting (
194 Our findings suggest the role of native species diversity in regulating nonnative pest invasions
195 he subfamily Chrysopinae includes 97% of the species diversity in the family and it is currently divi
198 n competitive ability and defense influenced species diversity in the manner predicted by theory.
199 of 1283 species, reveals that peak suboscine species diversity in the Neotropics is not associated wi
202 ield survey, we detect a twofold increase in species diversity in the surveyed area, at 42-45, with m
204 stability and high amplitude fluctuations of species diversity in the tropical deep ocean that are co
205 ts revealed potential hotspots of triatomine species diversity in tropical and subtropical regions be
206 ted a negative linear relationship with tree species diversity in two forest types, suggesting that s
207 hrough complementarity effects, whereas weed species diversity increased biomass predominantly throug
211 ions between environmental heterogeneity and species diversity indicate ubiquity of this phenomenon.
212 t we lack a mechanistic understanding of how species diversity influences decomposition processes.
213 the specific biological mechanisms by which species diversity influences nutrient uptake have not be
215 ng environmental factors in the radiation of species diversity is a fundamental question in evolution
216 tionary lineages generate exceptionally high species diversity is an important goal in evolutionary b
217 It is widely believed that this increase in species diversity is associated with increased intensity
219 rbital-scale oscillations in global climate: Species diversity is low during glacial and high during
222 , cloud forest, and paramo, where much plant species diversity is the hypothesized result of rapid sp
223 tural ecosystems, especially those for which species diversity is threatened by anthropogenic global
224 herbivores using insecticides did not alter species diversity, it greatly increased seedling recruit
225 torical factors, currents, productivity, and species diversity itself (through ecological interaction
226 ng interest in the origin and maintenance of species diversity, little is known about historical driv
227 in wild monkeys have high sequence and host species diversity, maintain high viremia, and are preval
229 n, indicate that morphological disparity and species diversity may be only weakly coupled in general,
230 ance enabling this progression is the use of species diversity metrics for quantifying phytochemical
231 have revealed large amounts of unrecognized species diversity, most of which is not represented in c
232 e collected revealed a significant amount of species diversity not seen in routine clinical laborator
234 significant correlations for abundances and species diversities of families and orders of trees on d
235 We used metabarcoding to estimate the fungal species diversities of naturally colonized decomposing w
236 The aim of this study was to determine the species diversity of 23 clinical isolates of Schizophyll
239 t past conditions for understanding the high species diversity of freshwater fish that we currently o
240 e the first description of the metabolic and species diversity of green and red snow algae communitie
244 through host-specific enemies, can influence species diversity of plant communities, but the generali
245 notype modulates both ROS production and the species diversity of the gut microbiome, implying that t
248 ot present a significant trend; however, the species diversity of woody plants decreased linearly tow
249 ese arguments have focused on the effects of species diversity on ecosystem stability but have not co
251 findings to assess the effects of increased species diversity on the patterns and processes of host
252 alone did not alter total community biomass, species diversity or community composition, whereas addi
253 content was not related to changes in plant species diversity or to the functional composition of th
254 plots, we show that mean temporal change in species diversity over periods of 5-261 y is not differe
255 ts in ecosystems require knowledge of within-species diversity, particularly of dominant species with
257 tterns of New World vertebrates and compared species diversity patterns between families that origina
261 lands (Kaua'i and O'ahu) have greater native species diversity per unit area than younger islands (Ma
262 ommunity stability can be achieved by higher species diversity (portfolio effect), higher asynchrony
263 the genus also increased, but not as fast as species diversity, possibly because of allopatric specie
264 hen ecological interactions presumably limit species diversity, potentially through diversity depende
265 sition is a primary determinant of the total species diversity present in a landscape, and thus, lowe
269 he 'dilution effect' proposes that increased species diversity reduces disease risk, suggesting that
270 years, fishing a set of permits with higher species diversity reduces individual revenue variability
271 tionship between natural variations in coral species diversity, reef development, and ecosystem funct
272 ldwide, we show that global patterns in tree species diversity reflect not only stronger CNDD at trop
273 We document unprecedented high levels of species-diversity, reflecting a global radiation since t
277 gated how trait variation shapes genetic and species diversity simultaneously in a tropical ecosystem
278 as determined through marked differences in species diversity, structure, distribution and compositi
279 y fields in the United States contained more species diversity than ever before reported on a single
280 old-growth grasslands support greater plant species diversity than secondary grasslands (i.e., herba
281 tracking data set of unprecedented scale and species diversity that covers 265,386 tracking days from
282 ent to generate a predictive distribution of species diversity that would be expected had the event n
283 rease in body size following the increase in species diversity through this interval: phosphatic brac
284 spective, we extend the theory developed for species diversity to further our understanding of what e
285 roposed to explain this unimodal response of species diversity to grazing intensity, no convincing ex
286 versity of life-history strategies and plant species diversity under different consumer regimes.
289 s to understand the ecological regulation of species diversity via bottom-up approaches have failed t
294 t to affect indoor fungal concentrations and species diversity, which are believed to increase the ri
295 rates are in lineages from regions with low species diversity, which are generally cold, dry, unstab
296 odels, such as mice and rats, and leveraging species diversity will allow us to use the genetic advan
298 to the classic latitudinal gradient of plant species diversity, with the proportion of mycorrhizal pl
300 nutrient supply promotes multistability and species diversity, yet make individual community states