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5 eas, through 1.6% (9.9 trees per hectare) in arid and 5.6% (30.1 trees per hectare) in semi-arid zone
11 reeding bird and small mammal communities in arid and mesic grasslands changed in response to increas
13 we demonstrate that internal deletion of the ARID and PHD1 domains has a negligible effect on in vitr
20 ple food for more than 90 million farmers in arid and semi-arid regions of sub-Saharan Africa, India
22 ce soil fertility and crop production in the arid and semi-arid regions stressed with water scarcity
23 ter salinization has been identified in many arid and semi-arid regions where groundwater is increasi
24 icant changes are occurring in the extensive arid and semi-arid regions, and we suggest that the repo
29 storical adaptation of sorghum production to arid and semiarid conditions has provided promise regard
32 sal of modern humans required the transit of arid and semiarid regions where the distribution of pota
36 otential mechanisms of abiotic CO2 uptake in arid and semiarid soils: atmospheric pressure pumping, c
37 d of the Pliocene, did the broad patterns of arid and semiarid subtropical regions become fully devel
39 entrated in rural rainfed systems throughout arid and temperate land across Eurasia, Africa and North
41 pattern of deteriorating environments (cool, arid, and anoxic conditions) and climate fluctuations ac
42 uced conversions among sub-humid, semi-arid, arid, and hyper-arid subtypes will lead to substantial c
43 the majority of C4 plants occupy disturbed, arid, and nutrient-poor habitats, some grow in high-nutr
44 the existing repertoire of genes involved in ARID, and provide new insights into the molecular mechan
45 frequently aseasonal, such as the tropical, arid, and semi-arid ecosystems that cover vast areas.
46 omogenization between the populations of the arid Andes is not only due to migrations during the Inca
47 f positive natural selection in the high and arid Andes vs. the low Amazon tropical forest: in the An
49 sed as storage for paraphernalia in the semi-arid area of the Judean desert and the dry conditions pr
51 sensitive to increased precipitation in more arid areas and more responsive to decreased precipitatio
52 ity of the final product, especially in semi-arid areas where irrigation water is scarce and/or of lo
53 n the mechanism of runoff generation in semi-arid areas while further experiments should be undertake
54 est increases in Rs and Q10 were observed in arid areas, and the stimulation rates decreased with inc
55 s from 0.1% (0.7 trees per hectare) in hyper-arid areas, through 1.6% (9.9 trees per hectare) in arid
56 te-induced conversions among sub-humid, semi-arid, arid, and hyper-arid subtypes will lead to substan
57 y increased nocturnal flight activity in the arid aseasonal ecosystem, but not in the mesic seasonal
63 arison Project Phase 5 (CMIP5) models to the arid basin (the Tarim River Basin, TRB) and humid basin
67 tree restoration potential across a third of arid biomes by between 7% and 20% (55-166 million hectar
68 s, however, emphasized dryland regions, with arid biomes making up 36%-42% of potential restoration a
70 with mycorrhizal fungi)-are most abundant in arid biomes with alkaline soils and high maximum tempera
71 South America (2,025 inventories from wet to arid biomes), and a new, large-scale phylogenetic hypoth
72 articipating in a case-control study in Semi-Arid Brazil, we identified key differences with potentia
73 N and P cycling and storage in semiarid and arid, but not in humid and dry-subhumid, environments.
74 in total profile SOC within a 1.8 km(2) semi-arid catchment in Idaho, U.S.A. can be explained as a fu
75 as sampled in 188 farm tubewells in the semi-arid catchment of Berambadi and in 5 piezometers in the
76 floristics, vegetation and climate change in arid Central Asia, cold arid alpine QTP, and mesophytic
77 UHI is 0.7+/-0.3 K (mean+/-1 s.e.) for semi-arid cities, which is stronger than that in the humid cl
79 developing Li brines with the combination of arid climate and the presence of landlocked extensional
83 fering in phenology, plants originating from arid climates bolted up to 48 d earlier than plants from
84 P in nitrogen per leaf area (Narea), even in arid climates, despite diazotrophy being sensitive to dr
85 waves threaten agricultural productivity in arid climates, our findings will facilitate identificati
90 its of central China support the presence of arid conditions and modern atmospheric pathways for the
92 ndicate that these sediments developed under arid conditions in which high marine alkalinity favoured
95 antibiotic resistance and virulence in more arid conditions suggests reduced intensity of biotic int
96 In terms of specific functions, more extreme arid conditions were also associated with increased rela
97 es that the secretion does not dry out under arid conditions, not melt at 50 degrees C, and not chang
100 ecies typify hot, sunny environments only in arid conditions; small leaves are also found in high lat
101 t source of groundwater salinization in semi-arid context, and stress that identifying dominant drive
102 e, well-watered routes into the semiarid and arid continental interior were available throughout the
104 els revealed that time-limited dispersal via arid corridors is a key predictor to explain macro-scale
106 eficial and pathogenic fungi in increasingly arid crop soils and, secondly, through promotion of phos
108 g winter and post-monsoon, especially in the arid desert and warm-temperate grasslands, the DTR decre
110 icrobial communities are ubiquitous in hyper-arid deserts around the world and the last resort for li
111 re is an atypical insertion of a DNA-binding ARID domain and a histone-binding PHD domain into the Ju
115 is paper, we examined the response of a semi-arid ecological community to a fivefold change in precip
117 st that natural coherent variability in semi-arid ecosystem productivity responded to ENSO in opposit
118 ay imply potential prediction of global semi-arid ecosystem variability, particularly based on variab
123 ncroachment in arctic, alpine, and arid/semi-arid ecosystems around the world, yet our understanding
124 a global hot spot for variability, with semi-arid ecosystems in that country exhibiting increased car
126 Our findings indicate that arid and semi-arid ecosystems may not be sensitive to CO(2) enrichment
128 hibits stronger and faster responses of semi-arid ecosystems to ENSO than the Northern Hemisphere.
129 lobal carbon fluxes may be dominated by semi-arid ecosystems, but the underlying mechanisms of this h
130 needed access to drinkable water to survive arid ecosystems, but were simultaneously constrained by
131 ers in underrepresented regions such as semi-arid ecosystems, forests in the tropics and subtropics,
133 e the impacts of ENSO on variability of semi-arid ecosystems, using the Ensemble Empirical Mode Decom
134 dge of anthrax ecology is largely limited to arid ecosystems, where outbreaks are most commonly repor
135 primary determinant of plant growth in semi-arid ecosystems, yet it remains difficult to forecast la
138 33-year-long dataset spanning a 1,267-m semi-arid elevational gradient in the southwestern United Sta
139 There is an increased risk of extremely arid environment and large deserts developed progressive
140 The long-term exposure of vegetation to this arid environment has favoured a resilient flora capable
141 goats and sheep that are indigenous to a hot arid environment in Egypt's Coastal Zone of the Western
142 re influence vital rates and viability of an arid environment specialist, the Kalahari meerkat, throu
143 orthern Africa) evolved from a predominantly arid environment with high-frequency variability to gene
147 ct a range of traits including adaptation to arid environments and defence against pathogens and toxi
148 rassulacean acid metabolism (CAM) evolved in arid environments as a water-saving alternative to C(3)
149 Our observations reveal that eucalypts in arid environments have thick amphistomatous leaves with
150 ts differing responses based on environment; arid environments in New Mexico see increased intrinsic
151 d angiosperms, we hypothesize that plants in arid environments may reduce dx:dy below unity owing to
152 Venice Lagoon to unvegetated systems in the arid environments of the Gulf of California and Yemen.
154 30 years) that is adapted to survive in semi-arid environments with varying levels of parasite exposu
155 ctly influenced traits for adaptation to hot arid environments, such as thermo-tolerance (melanogenes
160 and rivers with catchments across a humid to arid gradient covering >1,800,000 km(2) of continental e
161 nges of net ecosystem productivity in a semi-arid grassland despite whether temperature, precipitatio
163 that increased winter snowfall may stabilize arid grassland systems by reducing resource competition,
164 ent-specific community composition in a semi-arid grassland under long-term simulation of six differe
168 historic periods of sand deposition in semi-arid grasslands and external climatic conditions, land u
169 ignificantly across cold, temperate and semi-arid grasslands, in that responses for most C fluxes wer
173 northern India, diversifying into new, more arid habitats after environmental conditions stabilized.
175 mutations that cause autosomal recessive ID (ARID) has lagged behind, predominantly due to non-availa
176 ition from the wetter glacial period to more arid Holocene accompanies a surface warming of 6.2 +/- 0
177 initions of grazed livestock agroecosystems (arid, humid, and temperate), and groups of animal produc
182 phosphorus-SRP) along a approximately 300-km arid-land river (Rio Grande, NM) and generated nutrient
185 nexplained high rates of litter mass loss in arid lands; however, the global significance of this pro
186 rmed by unique features of the Mediterranean arid landscape, such as the dramatic ecological contrast
187 tal to the development of human societies in arid landscapes and for long-distance trade across hosti
189 were widespread and abundant throughout the arid landscapes of Central Asia and Mongolia, but have u
193 local coast and possess limited richness in arid (< 5% moisture) and at high elevation sites, known
194 arid Rwanda, hot subhumid Ghana and hot semi-arid Mali and Benin using an ensemble of 25 maize models
196 an be propagated from tropical areas to semi-arid Mediterranean biomes through atmospheric wave train
197 cadal shifts in forest carbon uptake in semi-arid Mediterranean pine forests in Spain over 1950-2012.
198 , and, as a result of its development in the arid Middle East, the ability to thrive in a hot, dry en
200 spatial range covering tropical, temperate, arid, montane and coastal environments from 9.25oS to 43
204 tant adaptation for early farmers in China's arid north, and that management practices like these lik
205 t mangroves and halophyte scrubs in Mexico's arid northwest, with less than 1% of the terrestrial are
206 the plot and hill slope scale as well as in arid or semi-arid climate conditions remain unclear.
208 Upper Gila Mountains and South-Central Semi-arid Prairies, and decreases in the north, particularly
212 yrah grape by-products, produced in the semi-arid region in Brazil, was optimized by a Central Compos
215 tic betaproteobacterium isolated from a semi-arid region of southern Tunisia, forms both rods and cys
217 E, large settlements were established in the arid region of the Negev Desert, Israel, but it remains
218 ) drive(s) the grassland restoration in semi-arid region, we investigated the relationships between p
221 the production of solar thermochemical fuels arid regions are best-suited, and for biofuels regions o
223 hat, relative to local conventional tillage, arid regions can benefit the most from conservation agri
225 ent attempts to map restoration potential in arid regions have been hindered by underlying errors in
228 Scarcity of fresh water in arid and semi-arid regions means that we must use more saline waters f
229 s of Agave, which are native to semiarid and arid regions of Central and North America and are emergi
231 ore than 90 million farmers in arid and semi-arid regions of sub-Saharan Africa, India and South Asia
232 bution and frequency of change within highly arid regions of the continental flyway increased their v
235 ity and crop production in the arid and semi-arid regions stressed with water scarcity and natural re
236 nix dactylifera L.) is a major fruit crop of arid regions that were domesticated ~7,000 y ago in the
237 r results demonstrate the importance of semi-arid regions to the global terrestrial carbon cycle and
238 on has been identified in many arid and semi-arid regions where groundwater is increasingly used for
239 d water use in seasonally dry, semiarid, and arid regions where precipitation and evapotranspiration
240 tence in wastewater treatment, especially in arid regions where treated municipal wastewater is exten
241 lts support that LSTs in semi-humid and semi-arid regions with little vegetation will be more sensiti
242 nd early-domesticated dromedary samples from arid regions with nuclear microsatellite and mitochondri
244 turnover of dead organic matter in soils of arid regions), reduce human exposure to mycotoxins in bu
245 are occurring in the extensive arid and semi-arid regions, and we suggest that the reported increased
246 nter-annual variability was observed in semi-arid regions, but croplands in China and India also show
249 cause attractive production locations are in arid regions, the water footprint and the land requireme
250 es in contributing to budgets of GHGs in the arid regions, whereas their global importance would be e
251 ta) is a legume species widely grown in semi-arid regions, which has high potential to provide stable
261 ific leaf area (SLA) shrubs with low K(s) in arid relative to tall large-leaved high-SLA trees with h
262 and hematite showed increased solubility at arid RH, but no difference (p > 0.05) was observed betwe
264 including cool subhumid Ethiopia, cool semi-arid Rwanda, hot subhumid Ghana and hot semi-arid Mali a
265 dy plant encroachment in arctic, alpine, and arid/semi-arid ecosystems around the world, yet our unde
266 ason precipitation for 2 y in field plots at arid, semiarid, and mesic grasslands to investigate temp
268 mammal, fish, reptile, and plant families in arid, semiarid, dry temperate, and Mediterranean ecosyst
271 (T) and LB41, isolated from an extreme hyper-arid soil collected from one of the driest regions of th
272 mic analyses of hyper-arid and extreme hyper-arid soils in this desert revealed a remarkable degree o
274 nobacteria typically colonize the surface of arid soils, building biological soil crust (biocrusts) t
275 le north, where altitudes are lower, and the arid south, where the Andes are higher, acting as a gene
278 inform paleoclimatic reconstructions for the arid southwestern US but are not typically preserved in
279 e trade-offs as soils transition toward more arid states is, therefore, critical to estimating global
281 among sub-humid, semi-arid, arid, and hyper-arid subtypes will lead to substantial changes in region
291 e grassland types (cold, temperate, and semi-arid), warming methods, and short (<=3 years) and longer
300 id and 5.6% (30.1 trees per hectare) in semi-arid zones, to 13.3% (47 trees per hectare) in sub-humid