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1 e foraging activity when conditions are more humid.
2 y traversodont cynodonts are restricted to a humid 6 degrees equatorial swath that persisted for over
3 esence of water and can be subjected to 1000 humid adsorption/desorption cycles with minimal degradat
7 investigated the byproducts generated by the humid air discharge itself, which are the greenhouse gas
8 27(5) A, beta = 97.41(3) degrees), formed in humid air from the solid dimeric [Cu(CF(3)COO)(2) x (qui
11 y condensation of the water molecules of the humid air on the paper-sensor during the forced exhalati
12 Binary CO2/H2O adsorption measurements for humid air reveal that the presence of H2O at 2.55 kPa en
16 bonyls into imines mediated by NH3 vapors in humid air, resulted in selective browning of the LSOA sa
17 dsorbed than long chain alcohols, whereas in humid air, this preference is changed, and the sensitivi
18 Pseudomonas putida, i.e., biofilms grown in humid air, were analyzed by atomic force microscopy to d
19 lved in surface-adsorbed water reservoirs in humid air, with the signal strength being governed by th
26 iad" of neurons (with a dry-, a cold-, and a humid-air-responding cell [3]), IR40a expression include
29 ng-term impact of NT/RT on N2 O emissions in humid and dry climatic zones with emissions expressed on
30 nvestigated at the gas/solid interface under humid and dry conditions, along with the nature of the h
33 Flash droughts are most likely to occur over humid and semi-humid regions, such as southern and north
34 y of humidity swing driven air capture under humid and windy conditions is tested in the laboratory.
35 ver a wide range of climate conditions (arid-humid) and limiting factors (soil moisture, leaf area, e
36 ens are intensifying (becoming more warm and humid), and thus changes in synoptic meteorology may be
39 130 degrees C) and working conditions (i.e., humid) as well as in the presence of various interfering
41 ples were subjected to an oxygenated, highly humid atmosphere in a closed chamber for 4 to 5 months.
42 mechanism is revealed to differ for dry and humid atmospheres, changing from a site-specific binding
44 ter droplets and films on the leaf hair from humid atmospheres; collection of fog droplets on leaf ha
45 arid basin (the Tarim River Basin, TRB) and humid basin (the Yangtze River Basin, YRB) were evaluate
46 rt of Pangea and suggest that the equatorial humid belt in the Late Triassic was about as wide as it
47 prolonged residence in the austral temperate humid belt where a provincial vertebrate fauna with earl
48 ble Deccan Traps drifted into the equatorial humid belt where uptake of CO(2) by efficient silicate w
53 r calculation remains large, particularly in humid catchments (for example, figure 2 in our paper).
54 0.51 kg C m(-2), lower than that observed in humid cities but much higher than that assumed in many r
55 d cities, which is stronger than that in the humid climate due to a stronger longwave radiative forci
56 cted rocks (mafic/ultramafic) and a tropical humid climate with high precipitation rate are needed to
57 te climate, hot and dry climate, and hot and humid climate) for at least 9 days simulating the period
59 +/- 0.3 kelvin (mean and standard error) in humid climates but decreasing DeltaT by 1.5 +/- 0.2 kelv
60 t decrease in yield-scaled N2 O emissions in humid climates when fertilizer-N was placed at >/=5 cm d
62 cts the species range limits in both dry and humid climates, whereas SLA and longevity do not show cl
65 s on the surface of an early Earth beneath a humid CO(2) atmosphere suffering electrical discharge.
68 n of atmospheric (CH3)2COO may survive under humid conditions and react with SO2, very different from
69 tilization models that already work well for humid conditions but still lack the mechanistically base
70 olumn breakthrough experiments under dry and humid conditions corroborate the excellent CO2 selectivi
71 ous and the subsequent onset of long-lasting humid conditions during the Late Cretaceous were driven
72 ly Holocene transition and increased as more humid conditions favored forest development after ca. 10
74 ons at the interface of hybrid systems under humid conditions has the potential to reveal the local c
75 years ago, coincident with the onset of more humid conditions in central Africa at the beginning of t
78 ith NO being the major product under dry and humid conditions in the absence of molecular oxygen and
79 s at the polymer/metal oxide interface under humid conditions is vital to understand the long-term du
81 mined on bean leaf surfaces maintained under humid conditions or periodically exposed to desiccation
82 jor rise in water levels and a shift to more humid conditions over much of tropical Africa after appr
83 O)2(dobdc), steadily releases bound NO under humid conditions over the course of more than 10 days, s
87 African climate changed rapidly towards more humid conditions, while northern sub-Saharan Africa expe
92 of vocal fold vibration in desiccated versus humid contexts, arid and cold ecologies should be less a
94 accumulation of soil nitrate in Chinese semi-humid croplands based upon more than 7000 samples from 1
95 nitrate reservoir in the vadose-zone of semi-humid croplands, where the nitrate cannot be denitrified
101 e less amenable, when contrasted to warm and humid ecologies, to the development of languages with ph
102 mpling design includes many plots located in humid ecosystems and ignores critical areas for the cons
104 s that Eoanabas likewise lived in a warm and humid environment as suggested by the co-existing plant
106 iscible, volatile solvent was deposited in a humid environment on a variety of substrates to achieve
107 , a mode of collective bacterial motility in humid environment through the depinning of bacterial dro
108 l coincides with paleoclimatic change from a humid environment to highly variable and much drier cond
110 effect of water was more pronounced at high humid environment, while at low RH the matrix plasticiza
113 occurring in agricultural workers in hot and humid environments may represent harbingers of the detri
117 ubsequent mud formation on solid surfaces in humid environments typically have adverse effects on sur
120 northward dispersal likely occurred during a humid episode in the Sahara within Marine Isotope Stage
121 hern margin of Amazonia, which show that the humid evergreen rain forests of eastern Bolivia have bee
127 limits of low proton affine analytes even in humid gas mixtures containing high proton affine compoun
129 ent with adjacent "hot," "cold," "dry," and "humid" glomeruli-an organization that allows for both un
131 oss of kleaf and turgor loss point) than the humid-habitat Ranunculus lanuginosus Accordingly, water
133 ies living in tropical, densely forested and humid habitats in Africa have evolved darker faces.
136 d, flies avoided dry heat more robustly than humid heat, and this modulation was abolished by silenci
137 across the menstrual cycle, yet is lower in humid heat, in conjunction with reduced evaporative cool
140 and mid-luteal (ML) phases in dry (DRY) and humid (HUM) heat matched for wet bulb globe temperature
142 northern and southern hemispheres, producing humid intervals in one hemisphere matched to aridity in
144 ing, reveal that landslide frequency in many humid landscapes may be insensitive to projected changes
146 the contemporary northern limit (colder and humid maritime regions; Denmark and Norway) will probabl
147 to the ecological opportunities provided by humid, megathermal forests, which were increasingly avai
148 radation upon exposure to dry air/oxygen and humid nitrogen/water environments, thus separating the e
153 of the onset and termination of the African Humid Period are contested, with strong evidence for bot
154 nd termination of the Early Holocene African Humid Period are subjects of ongoing debate, with direct
155 strong terrestrial evidence that the African Humid Period ended abruptly, supporting the hypothesis t
157 suggests that the termination of the African Humid Period in the Horn of Africa occurred within centu
158 hemispheric coherence of this early African Humid Period is challenging due to opposing seasonal ins
159 deposition of F- and Na+ during the African Humid Period suggests rapidly fluctuating lake levels be
160 sal was possible because during the Holocene humid period the region contained a series of linked lak
170 uggesting that any land cover changes in non-humid regions (P/PET<1) or in watersheds of low water re
172 are most likely to occur over humid and semi-humid regions, such as southern and northeastern China.
175 Here, we report the identification of the humid-responding neuron that completes the hygrosensory
176 n the Vaejovis vorhiesi group, restricted to humid rocky habitats in mountains across southwestern No
180 he school term in late May-June 2009 in more humid southeastern states), school vacations (preventing
182 outbreaks of pandemic influenza during more humid spring, summer, and autumn months might appear to
184 cal, predominantly deciduous), early Eocene (humid subtropical, mixed deciduous and evergreen), and m
185 cal patterns over topoclimate gradients in a humid temperate broadleaf forest in southern Appalachian
187 ated human malaria, including P. vivax, into humid temperate or warm climate refuges around the Medit
188 ly show that the Tortonian Europe mainly had humid to subhumid summers and no arid climate has been c
190 Oxisol soils are widely distributed in the humid tropical and subtropical regions and are generally
194 ca contributes 5.4% to the estimated loss of humid tropical forest cover, reflecting the absence of c
196 of redox fluctuations on lignin breakdown in humid tropical forest soils during ten-week laboratory i
198 Long-term monitoring of plots in mature humid tropical forests concentrated in South America rev
200 Psychotria marginata, a shrub common to humid tropical forests in Central America, produces leav
201 ntributes to rapid rates of C cycling across humid tropical forests in spite of periodic O2 limitatio
202 constant proportion (9%) of biomass, but in humid tropical forests this ratio varies from 2% in undi
203 ions for understanding the global ecology of humid tropical forests, and their functional responses t
204 fference between the two models occurred for humid tropical forests, where the CLM-CN simulated a 62%
207 omote forest regeneration and restoration in humid tropical lowland areas with high biomass resilienc
208 ed the largest area of GFCL, followed by the humid tropical, dry tropical, and temperate biomes.
209 esculenta) is an important root crop in the humid tropics and a valuable source of essential mineral
211 Extrapolation to perennial plants in the humid tropics is risky because functional relationships
218 nd 0.8 +/- 0.3 for rubber plantations in the humid tropics; and (ii) land use management policies sho
220 es and vegetation during the late Paleocene (humid, warm temperate to subtropical, predominantly deci
224 ly occur in hyper-arid zones and smallest in humid zones, highlighting the dependency on available su
225 cation of fossil-rich outcrops and temperate humid zones, indicating that climate change from arid to
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