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1 th of deciduous shrubs (dwarf birch and gray willow).
2 iterature for sieve elements in the stems of willow.
3 tration gradient in the minor vein phloem of willow.
4 iherbivore effects found only in poplars and willows.
5 trations E(23) observed in October for white willow (0-1800 mug kg(-1)), followed by black poplar (6.
7 okra, tomato, peanut, Indian hawthorn, ash, willow and elm trees (7 samples); M. marylandi Jepson &
8 40% removal of phenanthrene from soil by the willow and grasses, respectively inoculated with PD1 whe
9 eck impact, where only two scenarios, namely willow and Miscanthus co-firing, allowed for an improvem
10 s of intraspecific divergence within Cushion willow and possibly other alpine plants with a similar d
11 te how two common cold-adapted bird species, willow and rock ptarmigan (Lagopus lagopus and Lagopus m
12 up to 54% reduced GHG per hectare from using willow and switchgrass feedstock sources to produce etha
13 udy the control of bud activation in biomass willow and to assess similarities with the known hormone
15 erns contribute to the chemical diversity of willows and suggest that variable selective pressure acr
17 ous extracts revealed that Red Willow, White Willow, and White Oak KCNQ-dependently relaxed rat mesen
18 , Slippery Elm, White Oak, Red Willow, White Willow, and Wild Cherry each strongly activated KCNQ5 ex
26 (SLR) in Salix nigra, a basal species in the willow clade, and demonstrated that this species has XY
29 e evidence of the significant potential that willow could have in sustainable livestock production sy
31 t of $448 ha(-1) for ethanol production from willow, depending on varying biomass yield under differe
32 treatment study comparing grazing systems: a willow fodder mix with a grass understory (WFG) and pere
33 presented variation in traits of tetraploid willow genotypes provides a basis to use autopolyploidiz
35 for the first time, the feasibility of using willow grazing in a silvopastoral system to improve rumi
36 We show that differences in chemistry among willows growing at different elevations occur mainly thr
41 the genetic architecture of resistance in a willow hybrid system, Salix eriocephala, S. sericea, and
42 plars, the diversity of sex determination in willows is poorly understood, and little is known about
45 dies reported here, the minor vein phloem of willow leaves plasmolyzed in approximately the same conc
46 sphere, brain-like, groundnut-like and pussy willow-like morphologies were obtained through the synth
47 ound that the sex determination mechanism of willows may have underlying similarities with poplars, b
48 >5000 putative compounds, including 278 core willow metabolome compounds constitutively produced acro
51 Photoreforming perennial bioenergy crops (willow, Miscanthus, and poplar) has the potential to pro
53 is is the first time that the inoculation of willow plants has been shown to improve the degradation
54 y risk: (1) VHF telemetry data collected for willow ptarmigan in Alaska, and (2) hourly GPS telemetry
55 enius (woolly mammoth), and Lagopus lagopus (willow ptarmigan) eDNA from multiple permafrost cores sp
56 drogen production for different varieties of willow ranging between 1.9 mumol h(-1) and 12.3 mumol h(
57 pecific objectives were to: (a) characterise willow's CTs, and (b) explore their effect on methane em
61 and soluble isoprene synthases from a single willow (Salix discolor L.) leaf-fractionation protocol.
63 treeline birch (Betula pubescens) forest and willow (Salix lapponum) patches in northern Sweden and q
64 eezing sensitivity, and growth, for Lemmon's willow (Salix lemmonii) in a common garden study of 90 g
65 reated skin samples and samples treated with willow (Salix sp) bark extract and cod liver oil are com
67 fate in a subset of poplar (Populus sp.) and willow (Salix sp.) species revealed a broader distributi
69 the short-rotation coppice system in biomass willow (Salix spp.) relies on the activity of the shoot-
74 nt groupings of species (dwarf birch shrubs, willow shrubs, other deciduous shrubs, grasses, sedges,
76 e repeated turnovers keep sex chromosomes of willow species in a perpetually young state, leading to
81 s of swallows, and they drill sap wells into willows that provide abundant nourishment for themselves
82 structure) in which the highest ranking male willow tit is fourth in the overall hierarchy after the
83 Crested tits (Lophophanes cristatus) and willow tits (Poecile montanus) form mixed-species groups
84 , whereas in egalitarian groups, subordinate willow tits had significantly lower fat reserves and the
86 ominance structures occur in which the adult willow tits rank second and the hierarchy is less steep,
88 biomass response, and responses of birch and willow, to warming by 19%, 46%, and 11%, respectively.
90 elationship (SAR) study of the South African willow tree (Combretum caffrum) antineoplastic constitue
91 elationship (SAR) study of the South African willow tree (Combretum caffrum) antineoplastic constitue
93 vely, for vehicles fueled with corn stover-, willow tree-, and Brazilian sugarcane-derived ethanol, m
96 ze three divergent chromosome regions in the willow warbler Phylloscopus trochilus, of which two are
97 cale bird ringing data for one such species (willow warbler, Phylloscopus trochilus), we show that se
100 least efficacious extracts revealed that Red Willow, White Willow, and White Oak KCNQ-dependently rel
101 ch, Cramp Bark, Slippery Elm, White Oak, Red Willow, White Willow, and Wild Cherry each strongly acti