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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.
17 n enables deepwater rice to keep part of its foliage above the rising flood waters during the monsoon
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
23 ls of gossypol and related terpenoids in the foliage and floral parts were not diminished, and thus t
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
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
34 ain edible fruits and/or leaves from a green foliage background instead of relying on mobile insect p
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
51 ivory is the earliest occurrence of external foliage-feeding and galling in the terrestrial fossil re
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.
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
63 cedar) is a long-lived conifer species whose foliage is rarely affected by disease or insect pests, b
66 oids and isoprenoid compounds present in the foliage not only add nutritive factors to the feed but a
69 ase activity was higher in beetles consuming foliage of soybeans grown under elevated CO2 than in bee
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
75 fine-root production (NPPfroot ), NPPwood vs foliage production (NPPfoliage ), and autotrophic respir
77 bird predation vary with different levels of foliage productivity in the canopy vs. the understory.
79 Disruption of amino acid metabolism in Ni-D foliage resulted in accumulation of glycine, valine, iso
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
90 lations modifies contributions from soil and foliage to the global CO(18)O budget and eliminates pers
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
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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