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1 ble, warm and wetter climates (e.g. tropical rain forest).
2  with elevation in an Australian subtropical rain forest.
3 e and among species in a diverse Costa Rican rain forest.
4 r high-diversity areas, including the Amazon rain forest.
5 with the highest diversity found in tropical rain forests.
6 )-rich, phosphorus (P)-poor lowland tropical rain forests.
7 of the understory tree diversity in tropical rain forests.
8 he canopies of angiosperm-dominated tropical rain forests.
9 e three-dimensional (3D) structure of native rain forests.
10  fundamental 3D structure of native Hawaiian rain forests.
11 of magnitude lower than they are in tropical rain forests.
12 st of seed plant species from lowland Amazon rain forests.
13                                       Amazon rain forests accounted for 42% of the global increase in
14 rala coast and its differences with tropical rain forest and ocean microbiome.
15 pecies, which we predict will be frequent in rain forest and savanna, and which represent excellent c
16 often widespread species is more frequent in rain forests and is likely to reflect large effective po
17 belowground C storage and fluxes in tropical rain forests, and highlight differences between tropical
18 l fungi and tree communities in this Bornean rain forest assemble independently of host-specific inte
19 0, canopy tree growth in old-growth tropical rain forest at La Selva, Costa Rica, varied >2-fold amon
20 ment of modern angiosperm-dominated tropical rain forest canopies, or spurred on by some other large-
21                                          The rain forest canopy is a seamless web through which arbor
22 n in the Andes has focused on biomes such as rain forest, cloud forest, and paramo, where much plant
23 rtion of tree species in neotropical lowland rain forest communities as measured in complete plot cen
24 trees with AMF or EMF symbioses in a Bornean rain forest containing species with both mycorrhizal str
25  water availability gradient from deserts to rain forests dictates turnover of lineages within contin
26  is essential for understanding the cause of rain forest diversity and its potential as a methane sou
27 inct preference for semi-open rainforest and rain forest edges.
28                                         This rain forest expansion is attributed to increased seasona
29                 Although outsiders value the rain forest for its high-use and non-use values, local p
30 tured under natural conditions in a tropical rain-forest for dynamic ant behavior study.
31  disparate mangrove forests and the tropical rain forest, from the ocean.
32                Over two years, in a tropical rain forest in Costa Rica (La Selva Biological Station),
33 erfall manipulation experiment in a tropical rain forest in Costa Rica to test the sensitivity of sur
34 lates soil respiration in a lowland tropical rain forest in Costa Rica.
35 f a blowdown disturbance on ACD in a lowland rain forest in Costa Rica.
36 show further that fragmentation of Amazonian rain forests in the Pleistocene, if it occurred, appears
37 ree major habitat types of lowland Amazonian rain forest, including terra firme clay, white-sand and
38 of forest canopies across a Hawaiian montane rain forest landscape.
39 s-rich low latitude biomes (such as tropical rain-forests) less resilient to major disturbances.
40  are displayed here from the dry, cloud, and rain forests of Area de Conservacion Guanacaste (ACG) in
41 ciates in the 1,260 km(2) of dry, cloud, and rain forests of Area de Conservacion Guanacaste (ACG) in
42 mazonia, which show that the humid evergreen rain forests of eastern Bolivia have been expanding sout
43  is cosmopolitan, and relatives in Colombian rain forests of South America could be the source of the
44  number of plant species in the vast lowland rain forests of the Amazon have been based largely on mo
45 cross a seasonal cycle in a tropical lowland rain forest on Barro Colorado Nature Monument (BCNM), Re
46 ee than Pongo sp., which inhabited monsoonal rain forests on Java.
47 resents the southernmost extent of Amazonian rain forest over at least the past 50,000 years.
48 m ages and lack of geographical structure in rain forest phylogenies may reflect more widespread dist
49 y of a natural plant extract from the Amazon rain forest plant (i.e. Uncaria tomentosa or cat's claw)
50 ailed, comprehensive consumption patterns of rain forest products by an indigenous population and the
51    By contrast, the Guineo-Congolian lowland rain forest region is characterized by widespread and ol
52     Human monkeypox is an endemic disease in rain-forested regions of central Democratic Republic of
53                                    Amazonian rain forest-savanna boundaries are highly sensitive to c
54 ngal pathogens of plant leaves in a tropical rain forest show that most fungal pathogens are polyphag
55 station nearly halved and tropical moist and rain forest sites showed moderate losses around 10% by t
56           Under SSP2-4.5, tropical moist and rain forest sites were resilient and tropical dry forest
57 ixers and non-fixers in two lowland tropical rain forest sites, but also addressed the hypothesis tha
58 cent genes from Enterobacter lignolyticus, a rain forest soil bacterium that is tolerant to an imidaz
59  a lignocellulolytic bacterium from tropical rain forest soil, and report here that it can grow in th
60 hange and may also play an important role in rain forest speciation.
61 hin different climatic bioregions - tropical rain forest, sub-tropical evergreen broad-leaved forest
62 d other tree genera in Amazonian and Guianan rain forests suggests that speciation is not driven by v
63                                   The Amazon rain forest sustains the world's highest tree diversity,
64  people are paid for the non-local values of rain forests, they may be easily persuaded to deforest.
65       Here we have measured the value of the rain forest to local populations by monitoring the foods
66 rehensive estimates of the economic value of rain forests to assess conservation and management optio
67    Melicope xanthoxyloides is the Australian rain forest tree of the Rutaceae family in which evolidi
68 y, the only source of tigilanol tiglate is a rain forest tree, Fontainea picrosperma, whose limited n
69 econd-largest expanse of continuous tropical rain forest (TRF) in the world is found in Central Afric
70 ic and natural plant extract from the Amazon rain forest, was identified as a potent inhibitor and re
71 from airborne lidar in a lowland Neotropical rain forest, we quantify vertical leaf-area profiles and
72 ediment and a single isolate from a tropical rain forest were included in the analysis, a strong patt
73 om plant collection obtained from the Amazon rain forest yielded five plants that stimulated glycosam