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1  piceol and pungenol constitutively in their foliage.
2 lated with a significant increase of FPBs in foliage.
3 ound evidence for N2 fixation in P. flexilis foliage.
4 in detecting yellow/orange/red foods against foliage.
5 ting that C. cochlioides rapidly infects new foliage.
6 ne protease inhibitors) expressed in soybean foliage.
7 f antioxidant enzyme activities in coriander foliage.
8 s) deterring WCR beetles from devouring corn foliage.
9  and bioaccessibilities from fresh and dried foliage.
10 l as two flavonoid biosynthetic genes in the foliage.
11  identified from JB collected from grapevine foliage.
12  very low levels of citrate compared to Ni-S foliage.
13 pecializing on arthropods that consume plant foliage.
14  indioside D, that is present in solanaceous foliage.
15 is allocated to short-lived tissues, largely foliage.
16 ion upon partial submergence to maintain its foliage above the rising flood water levels.
17 n enables deepwater rice to keep part of its foliage above the rising flood waters during the monsoon
18             In evergreen conifers, where the foliage amount changes little with season, accurate dete
19            Furthermore, larvae consumed more foliage and attained larger masses when feeding on LapA-
20 ribute to the characteristic aroma of tomato foliage and constitute a key part of the language by whi
21 nated seedling of cv Sangrado that has green foliage and develops red flesh in the fruit cortex late
22                 M. sexta larvae damaged less foliage and displayed delays in growth and development w
23 ls of gossypol and related terpenoids in the foliage and floral parts were not diminished, and thus t
24 n to 32 and 14% of wild-type levels in plant foliage and seeds, respectively.
25 imilar dependence on logKOA as that of plant foliage and soil data.
26 , traditional measures of Ca availability in foliage and soil exchangeable pools may poorly reflect l
27 e mortality, while the loss of live wood and foliage and their respiration drove the decline of the c
28 xplained 30.7 and 13.6% of the variation for foliage and tuber blight on an additive model.
29   When the residuals from the regressions of foliage and tuber blight on maturity were analyzed, ther
30 omes: one for taxa with deciduous, palatable foliage, and the other for hosts with evergreen, thick-t
31 or has been shown to control fruit flesh and foliage anthocyanin pigmentation (MYB10) and fruit skin
32  than light limited, shade leaves and sunlit foliage are more abundant in the upper canopy.
33 ers or rhizomes of Dioscorea, neglecting the foliage as waste.
34 ain edible fruits and/or leaves from a green foliage background instead of relying on mobile insect p
35 ees to die, liquefy, and "rain" virus on the foliage below to infect new hosts.
36  even more of the variation, up to 37.2% for foliage blight.
37 tion for maturity, height, tuber blight, and foliage blight.
38 derived oxylipin promotes infestation of the foliage by GPAs.
39                          Ingestion of tomato foliage by specialist (Manduca sexta) and generalist (Tr
40 stance at which objects--prey, predators, or foliage--can be resolved.
41     Large-scale DNA sequencing of samples of foliage collected in the 19th century from plants infect
42  the second stage of respiration, where Ni-D foliage contained very low levels of citrate compared to
43 ggests that chewing damage on mountain birch foliage could significantly increase reactive VOC emissi
44 ctions, connectivity to adjacent forest, and foliage cover.
45               Cucumber is vulnerable to many foliage diseases.
46          Concentrations of (210)Pb and Hg in foliage double from 760 to 900 m elevation, indicating e
47 differences in aerodynamic attributes (e.g., foliage drag) were accounted for.
48                 The use of cleaner matrices (foliage, exposed smooth surfaces, sand) is recommended f
49                       Spectral properties of foliage express fundamental chemical interactions of can
50                           However, senescent foliage falling from treated trees represents a rarely s
51 ivory is the earliest occurrence of external foliage-feeding and galling in the terrestrial fossil re
52 al forest of whether birds indirectly defend foliage from arthropod herbivores.
53 way, neonicotinoid residues were analyzed in foliage from black alder trees treated with one of three
54 mon polyphenolic polymers of plants found in foliage, fruit, bark, roots, rhizomes, and seed coats th
55  In a Mexican coffee plantation, we excluded foliage-gleaning bird and bat predators from coffee plan
56 the lineages of Higher Reduviidae; living on foliage has evolved at least six times independently.
57                     Collecting and analyzing foliage in 2,420 canopy tree species across 19 forests i
58 stent with previously reported data of v for foliage in forest canopies after normalization on leaf a
59 nol and piceol commonly accumulate in spruce foliage in the form of the corresponding glycosides, pun
60 onsequence of remobilization from introduced foliage (input: 600 g foliage/m(2) containing 80 mug imi
61 riments demonstrated that GPA performance on foliage is influenced by the LOX5 genotype in roots, thu
62                         Conversely, the corn foliage is largely neglected as a food source by WCR bee
63 cedar) is a long-lived conifer species whose foliage is rarely affected by disease or insect pests, b
64 zation from introduced foliage (input: 600 g foliage/m(2) containing 80 mug imidacloprid/g).
65       Additionally, we show the potential of foliage material as a renewable source of high-value com
66 oids and isoprenoid compounds present in the foliage not only add nutritive factors to the feed but a
67                                              Foliage of Coriandrum sativum is a rich source of natura
68                                              Foliage of Ni-D pecan seedlings exhibited metabolic disr
69 ase activity was higher in beetles consuming foliage of soybeans grown under elevated CO2 than in bee
70 ds accumulate in glandular structures in the foliage of WRC.
71 eport that the N content of soils and forest foliage on N-rich metasedimentary rocks (350-950 mg N kg
72 processes that remove (7)Be and (210)Pb from foliage operate with a maximum half-time of greater than
73 se in bioaccessibility was observed in dried foliage, over twofold increase of each form of folate up
74 ance to nematodes and, in some instances, to foliage pathogens.
75 fine-root production (NPPfroot ), NPPwood vs foliage production (NPPfoliage ), and autotrophic respir
76 elopment and through stabilization of annual foliage production.
77 bird predation vary with different levels of foliage productivity in the canopy vs. the understory.
78                     Related proteins include foliage proteins and seed storage proteins.
79  Disruption of amino acid metabolism in Ni-D foliage resulted in accumulation of glycine, valine, iso
80      Disruption of ureide catabolism in Ni-D foliage resulted in accumulation of xanthine, allantoic
81            Root concentration factors (RCF), foliage/root concentration factors (FRCF), and transpira
82 rategies, S, of allocation of energy between foliage, roots, and wood.
83         Recovery of agent was optimized from foliage, sand, and glass in a simulated biothreat scenar
84 , as caused by roots becoming waterlogged or foliage submergence, triggers changes in gene transcript
85 yte presence, particularly in newly infected foliage, suggests that endophytes elicit similar chemica
86 ransferred from the nutrient solution to the foliage than shorter-chain PFCAs (e.g., perfluoroheptano
87 ptional response systemically induced in the foliage that prepares plants for future pathogen attack
88 ated concentrations in air, soil, water, and foliage that tend to fall close to or below the minimum
89      By changing the chemical composition of foliage, the increase in atmospheric CO(2) is fundamenta
90 lations modifies contributions from soil and foliage to the global CO(18)O budget and eliminates pers
91 here twofold increase in folates occurred in foliage upon SA treatment.
92              Ectopic expression of MYB305 in foliage was able to induce expression of both nec1 and n
93 ures causing higher uptake capacity of plant foliage, whereas cold-trapping in soils more strongly de
94 ew of the Morus species are valued for their foliage, which constitutes the chief feed for mulberry s
95 tural folates from this traditional culinary foliage, which is widely used in many cuisines.
96 rs (BCFs; plant/soil ratios) were highest in foliage, while the total tree burden of summation operat
97 0 genes that are expressed at high levels in foliage with glands, but can either not be detected or a
98 we solve the model for competitively optimal foliage, wood, and fine root allocation strategies for t
99 ously successful in predicting allocation to foliage, wood, and fine roots along natural productivity
100 itively driven changes in tree allocation to foliage, wood, and fine roots, either via plastic change
101 ion during the growth season, developed from foliage, wood, and soil CO2 efflux measurements, decline

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