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1  foliage paired with females with or without foliage).
2 l as two flavonoid biosynthetic genes in the foliage.
3  identified from JB collected from grapevine foliage.
4  very low levels of citrate compared to Ni-S foliage.
5 pecializing on arthropods that consume plant foliage.
6  indioside D, that is present in solanaceous foliage.
7 is allocated to short-lived tissues, largely foliage.
8 lowers contrasted more with bare ground than foliage.
9 iminate the depths of objects hidden beneath foliage.
10 ry combustion of boreal peat and live spruce foliage.
11  thereby produce a hue that perfectly mimics foliage.
12 ic video because of the occlusions caused by foliage.
13 esents typically less than 1% of total Hg in foliage.
14 ot significantly affected by the presence of foliage.
15 tion of P. monophylla from juvenile to adult foliage.
16 redressed their sterol deficit by feeding on foliage.
17  piceol and pungenol constitutively in their foliage.
18 lated with a significant increase of FPBs in foliage.
19 ound evidence for N2 fixation in P. flexilis foliage.
20 in detecting yellow/orange/red foods against foliage.
21 ounts of shaded foliage relative to full-sun foliage.
22 ting that C. cochlioides rapidly infects new foliage.
23 ne protease inhibitors) expressed in soybean foliage.
24 f antioxidant enzyme activities in coriander foliage.
25 s) deterring WCR beetles from devouring corn foliage.
26  and bioaccessibilities from fresh and dried foliage.
27 ion upon partial submergence to maintain its foliage above the rising flood water levels.
28 n enables deepwater rice to keep part of its foliage above the rising flood waters during the monsoon
29 in turn are possibly associated with sterile foliage allocated to Liaoningcladus.
30             In evergreen conifers, where the foliage amount changes little with season, accurate dete
31 ons instead of simply dropping them from the foliage (ancestral state).
32            Furthermore, larvae consumed more foliage and attained larger masses when feeding on LapA-
33  to encourage use of unified terminology for foliage and bud necrosis resulting from fire.
34 ribute to the characteristic aroma of tomato foliage and constitute a key part of the language by whi
35 nated seedling of cv Sangrado that has green foliage and develops red flesh in the fruit cortex late
36                 M. sexta larvae damaged less foliage and displayed delays in growth and development w
37 ls of gossypol and related terpenoids in the foliage and floral parts were not diminished, and thus t
38 ants, providing color to flowers, fruit, and foliage and helping to counter the harmful effects of en
39  bioconcentration of airborne xenobiotics in foliage and in air-breathing organisms.
40 nd isotope compositions of GEM as well as in foliage and litter samples.
41                The (228)Th:(228)Ra ratios of foliage and organic soil horizons evolve with time follo
42 tles often consume non-prey foods like plant foliage and pollen.
43                          We attributed wood, foliage and root carbon to every tree in the 0-1,000 mm
44 n to 32 and 14% of wild-type levels in plant foliage and seeds, respectively.
45 s and tree trunks, whereas white fur matches foliage and snow when present, and intermediate pelage t
46 imilar dependence on logKOA as that of plant foliage and soil data.
47 , traditional measures of Ca availability in foliage and soil exchangeable pools may poorly reflect l
48 e mortality, while the loss of live wood and foliage and their respiration drove the decline of the c
49 xplained 30.7 and 13.6% of the variation for foliage and tuber blight on an additive model.
50   When the residuals from the regressions of foliage and tuber blight on maturity were analyzed, ther
51 ly blight symptom development in both potato foliage and tubers.
52  communication, detoxification of food plant foliage, and immunity.
53  and methylmercury in the atmosphere, canopy foliage, and soils.
54 omes: one for taxa with deciduous, palatable foliage, and the other for hosts with evergreen, thick-t
55                              Combinations of foliage- and fruit-based compounds may be needed to incr
56  the response of adult Drosophila suzukii to foliage- and fruit-based synthetic compounds tested alon
57 species reared on pea aphids-with or without foliage-and compared their sterol profile to field-colle
58 or has been shown to control fruit flesh and foliage anthocyanin pigmentation (MYB10) and fruit skin
59 pplication of acetylsalicylic acid (ASA) via foliage application (FA), which promote plant growth and
60 irements) as a main plot, two ASA levels (No foliage application (NFA) 0 and 0.5 mM) as sub plot, and
61                Ambient MeSA accumulation and foliage application can effectively induce defense gene
62  than light limited, shade leaves and sunlit foliage are more abundant in the upper canopy.
63 owth can benefit summer growth by increasing foliage area and carbon sequestration potential, or impa
64          This reflected differences in total foliage area, rather than in self-shading.
65 old climates, and displayed larger effective foliage areas per unit of aboveground biomass, indicatin
66  (but frost-sensitive) xylem to deploy large foliage areas without increasing self-shading.
67 ers or rhizomes of Dioscorea, neglecting the foliage as waste.
68 ain edible fruits and/or leaves from a green foliage background instead of relying on mobile insect p
69 monstrate the use of biomonitors (i.e., tree foliage, bark, mosses, and lichens) in the Himalayas to
70 f the role of the microbial community on the foliage before litter fall (i.e. the phyllosphere commun
71 ees to die, liquefy, and "rain" virus on the foliage below to infect new hosts.
72  even more of the variation, up to 37.2% for foliage blight.
73 tion for maturity, height, tuber blight, and foliage blight.
74 ferent heights, roosting in sites underneath foliage, bumblebee hive usage) and interactions (parasit
75 derived oxylipin promotes infestation of the foliage by GPAs.
76                          Ingestion of tomato foliage by specialist (Manduca sexta) and generalist (Tr
77 stance at which objects--prey, predators, or foliage--can be resolved.
78     Large-scale DNA sequencing of samples of foliage collected in the 19th century from plants infect
79 heep grazing and/or hay cutting on arthropod foliage communities and flora within Welsh upland perman
80  the second stage of respiration, where Ni-D foliage contained very low levels of citrate compared to
81 al interpolations of PFAS in groundwater and foliage correspond well and demonstrate the successful a
82 ggests that chewing damage on mountain birch foliage could significantly increase reactive VOC emissi
83 ctions, connectivity to adjacent forest, and foliage cover.
84 rthermore, the underlying mechanisms causing foliage death from fire are poorly understood.
85               Cucumber is vulnerable to many foliage diseases.
86          Concentrations of (210)Pb and Hg in foliage double from 760 to 900 m elevation, indicating e
87 differences in aerodynamic attributes (e.g., foliage drag) were accounted for.
88 lent and motionless prey resting directly on foliage due to the masking effects of background echoes
89  example, are hypothesized to track seasonal foliage dynamics over large spatial scales.
90 the physiological basis for crypsis in green foliage even under near-infrared light.
91                         Therefore, stems and foliage experience repetitive mechanical stresses throug
92                 The use of cleaner matrices (foliage, exposed smooth surfaces, sand) is recommended f
93                       Spectral properties of foliage express fundamental chemical interactions of can
94                           However, senescent foliage falling from treated trees represents a rarely s
95 ivory is the earliest occurrence of external foliage-feeding and galling in the terrestrial fossil re
96 sparities between nearby objects and distant foliage for a hybrid control strategy: "ground-fixate, o
97 rha were generally lower in larvae reared on foliage from aCO(2) plants and higher in larvae reared o
98 al forest of whether birds indirectly defend foliage from arthropod herbivores.
99 way, neonicotinoid residues were analyzed in foliage from black alder trees treated with one of three
100 rgin female A. biguttatus prefer the odor of foliage from declining oaks compared with that from asym
101 aCO(2) plants and higher in larvae reared on foliage from eCO(2) plants.
102 ere, we describe a trace fossil on seed-fern foliage from the Rhode Island Formation of Massachusetts
103 mon polyphenolic polymers of plants found in foliage, fruit, bark, roots, rhizomes, and seed coats th
104 pring than in autumn, and more frequently in foliage gleaners.
105  In a Mexican coffee plantation, we excluded foliage-gleaning bird and bat predators from coffee plan
106                             More sun-exposed foliage had lower intercepts and slopes of the relations
107 the lineages of Higher Reduviidae; living on foliage has evolved at least six times independently.
108                     Collecting and analyzing foliage in 2,420 canopy tree species across 19 forests i
109 stent with previously reported data of v for foliage in forest canopies after normalization on leaf a
110 nol and piceol commonly accumulate in spruce foliage in the form of the corresponding glycosides, pun
111 onsequence of remobilization from introduced foliage (input: 600 g foliage/m(2) containing 80 mug imi
112  the end of the growing season, proving that foliage is a net accumulator of MeHg while foliar gain o
113 riments demonstrated that GPA performance on foliage is influenced by the LOX5 genotype in roots, thu
114                         Conversely, the corn foliage is largely neglected as a food source by WCR bee
115 cedar) is a long-lived conifer species whose foliage is rarely affected by disease or insect pests, b
116 zation from introduced foliage (input: 600 g foliage/m(2) containing 80 mug imidacloprid/g).
117 ke available a linked database of wood mass, foliage mass, root mass and carbon stock of each tree fo
118       Additionally, we show the potential of foliage material as a renewable source of high-value com
119                 Methane emissions from plant foliage may play an important role in the global methane
120 s and plant taxa (n = 131), with 83 distinct foliage morphotypes.
121 d LFMC dynamics as well as the occurrence of foliage mortality in a Mediterranean Quercus ilex forest
122 ier, our results showed that drought-induced foliage mortality is expected to increase, thereby signi
123 lnerability curves to cavitation to simulate foliage mortality.
124 oids and isoprenoid compounds present in the foliage not only add nutritive factors to the feed but a
125                                              Foliage of Coriandrum sativum is a rich source of natura
126                                              Foliage of Ni-D pecan seedlings exhibited metabolic disr
127                                     The dead foliage of scorched crowns is one of the most conspicuou
128 ase activity was higher in beetles consuming foliage of soybeans grown under elevated CO2 than in bee
129                                              Foliage of three species, namely, white willow (Salix al
130 ds accumulate in glandular structures in the foliage of WRC.
131 eport that the N content of soils and forest foliage on N-rich metasedimentary rocks (350-950 mg N kg
132 ins and lipids that generates an omnipresent foliage on the cell surface.
133 processes that remove (7)Be and (210)Pb from foliage operate with a maximum half-time of greater than
134 se in bioaccessibility was observed in dried foliage, over twofold increase of each form of folate up
135  x 2 factorial design (males with or without foliage paired with females with or without foliage).
136 cies influence nutrient dynamics in soil and foliage, particularly regarding nutrient retranslocation
137 ance to nematodes and, in some instances, to foliage pathogens.
138 hids in the presence or absence of fava bean foliage; pea aphids have very low sterol content.
139 conducted on dwarf schefflera, an ornamental foliage plant, which was exposed to foliar application o
140                                   Ornamental foliage plants that have a dense appearance are highly v
141 y flower against bare substrates rather than foliage, potentially impacting signal transmission and p
142 fine-root production (NPPfroot ), NPPwood vs foliage production (NPPfoliage ), and autotrophic respir
143 elopment and through stabilization of annual foliage production.
144 bird predation vary with different levels of foliage productivity in the canopy vs. the understory.
145 ty to ecosystem type in plant area index and foliage profile estimates that translate to c. 25% and c
146                     Related proteins include foliage proteins and seed storage proteins.
147 umed significantly greater amounts of shaded foliage relative to full-sun foliage.
148  Disruption of amino acid metabolism in Ni-D foliage resulted in accumulation of glycine, valine, iso
149      Disruption of ureide catabolism in Ni-D foliage resulted in accumulation of xanthine, allantoic
150                     As a migratory, cryptic, foliage-roosting bat with a mostly solitary roosting beh
151            Root concentration factors (RCF), foliage/root concentration factors (FRCF), and transpira
152 rategies, S, of allocation of energy between foliage, roots, and wood.
153         Recovery of agent was optimized from foliage, sand, and glass in a simulated biothreat scenar
154     Given the omnipresence of HG and RG-I in foliage, Stammera that encode pectinases targeting both
155 , as caused by roots becoming waterlogged or foliage submergence, triggers changes in gene transcript
156 yte presence, particularly in newly infected foliage, suggests that endophytes elicit similar chemica
157                             Females mated to foliage-supplemented males laid more eggs and more viabl
158                                              Foliage-supplemented males produced 2.9-4.6 times more s
159                                              Foliage supplements lengthened the development times of
160 s, we observed a profound paternal effect of foliage supplements on fitness.
161 e re-examine the morphology of the enigmatic foliage taxon Furcula, a potential early Mesozoic angios
162 ransferred from the nutrient solution to the foliage than shorter-chain PFCAs (e.g., perfluoroheptano
163 ptional response systemically induced in the foliage that prepares plants for future pathogen attack
164 ated concentrations in air, soil, water, and foliage that tend to fall close to or below the minimum
165      By changing the chemical composition of foliage, the increase in atmospheric CO(2) is fundamenta
166 One species, Coccinella septempunctata, eats foliage to redress sterol deficits caused by eating ster
167 lations modifies contributions from soil and foliage to the global CO(18)O budget and eliminates pers
168 st century has driven this temporal shift in foliage traits known to be physiologically critical to g
169 . pseudoinsulata did not differ according to foliage types.
170 est that the loss of exogenous immunity from foliage under eCO(2) results in increased endogenous imm
171 here twofold increase in folates occurred in foliage upon SA treatment.
172 (ambient vs reduced) and floral backgrounds (foliage vs bare) on pollinator choice for UV guide size.
173              Ectopic expression of MYB305 in foliage was able to induce expression of both nec1 and n
174 f cyantraniliprole primarily occurred in the foliage, where 21 metabolites were tentatively identifie
175 ures causing higher uptake capacity of plant foliage, whereas cold-trapping in soils more strongly de
176 ew of the Morus species are valued for their foliage, which constitutes the chief feed for mulberry s
177 tural folates from this traditional culinary foliage, which is widely used in many cuisines.
178 emporal dynamics and origins of MeHg in tree foliage, which represents typically less than 1% of tota
179 rs (BCFs; plant/soil ratios) were highest in foliage, while the total tree burden of summation operat
180 0 genes that are expressed at high levels in foliage with glands, but can either not be detected or a
181 we solve the model for competitively optimal foliage, wood, and fine root allocation strategies for t
182 ously successful in predicting allocation to foliage, wood, and fine roots along natural productivity
183 itively driven changes in tree allocation to foliage, wood, and fine roots, either via plastic change
184 ion during the growth season, developed from foliage, wood, and soil CO2 efflux measurements, decline

 
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