ライフサイエンスコーパス: Abies

1 h cellulose surfaces in Norway spruce (Picea abies).

2 aptation of the conifer Norway spruce (Picea abies).

3 resence of two PaLAR3 allelic lineages in P. abies.

4 sely related to linalool synthase from Picea abies.

5 leaf carbon dynamics in Norway spruce (Picea abies), a dominant northern forest species, to improve p

6 Although Silver fir (Abies alba) and Douglas fir (Pseudotsuga menziesii) have

7 Using needles of silver fir (Abies alba) seedlings as test subjects, we show that the

8 es, Norway spruce (Picea abies), silver fir (Abies alba), and European beech (Fagus sylvatica).

9 "winners"-mostly late-successional species: Abies alba, Fagus sylvatica, Fraxinus excelsior, Quercus

10 ate of three major tree species (silver fir, Abies alba; Scots pine, Pinus sylvestris; and mountain p

11 ots pine [Pinus sylvestris], and silver fir [Abies alba]).

12 at 50% loss of hydraulic conductivity in P. abies and P. mugo was -3.35 and -3.86 MPa at gamma of 74

13 seasonal changes in xylem sap gamma in Picea abies and Pinus mugo growing at the alpine timberline.

14 NA population from the conifer spruce (Picea abies) and compared the results with those of a range of

15 ncluding the gymnosperm Norway spruce (Picea abies) and the angiosperms rice (Oryza sativa), tobacco

16 spruce (Picea glauca), Norway spruce (Picea abies), and loblolly pine (Pinus taeda).

17 s, we isolated KCBP from a gymnosperm, Picea abies, and a green alga, Stichococcus bacillaris.

18 pecies: Betula pendula, Larix decidua, Picea abies, and Pinus sylvestris; and alien species-Pseudotsu

19 nt tree species such as Norway spruce (Picea abies) are required, if the frequency and intensity of s

20 ng juvenile period, for Norway spruce (Picea abies) around 20 to 25 years, before developing male and

21 e sampled the roots of Betula papyrifera and Abies balsamea saplings growing in the B4Warmed (Boreal

22 ent of the aromatic oleoresin of balsam fir (Abies balsamea) and serves as a valuable bioproduct mate

23 opulus spp.) or to biotic disturbances (e.g. Abies balsamea).

24 wave-regenerating populations of balsam fir, Abies balsamea, in order to estimate Ne/N.

25 birch (Betula pendula), Norway spruce (Picea abies), bird cherry (Prunus padus), mountain ash (Sorbus

26 Using detritus from Pinus ponderosa and Abies concolor (dominant species in forests in the weste

27 crobial taxa in the functioning of the Picea abies-dominated coniferous forest soil in two contrastin

28 genetic studies have suggested a role for P. abies FLOWERING LOCUS T/TERMINAL FLOWER1-Like2 (PaFTL2)

29 Norway spruce (Picea abies) forests suffer periodic fatal attacks by the bark

30 a(13) C and delta(18) O series of Smith fir (Abies georgei var. smithii) on the southeastern Tibetan

31 Abietadiene synthase from Abies grandis (AgAS) is a model system for diterpene syn

32 (15)), and abietadiene synthase (C(20)) from Abies grandis and taxadiene synthase (C(20)) from Taxus

33 Grand fir (Abies grandis Lindl.) has been developed as a model syst

34 geranyl diphosphate synthase from the plant Abies grandis was expressed to optimize the limonene bio

35 hosphate synthases from Taxus canadensis and Abies grandis yielded a functional hybrid heterodimer th

36 Grand fir (Abies grandis) has been developed as a model system for

37 Grand fir (Abies grandis) has been developed as a model system for

38 The oleoresin secreted by grand fir (Abies grandis) is composed of resin acids derived largel

39 ucible sesquiterpene synthases of grand fir (Abies grandis), and the olefin product of this cyclizati

40 und-induced oleoresin secreted by grand fir (Abies grandis), is synthesized by the cyclization of ger

41 tep of resin acid biosynthesis in grand fir (Abies grandis).

42 ield experiments during late winter on Picea abies growing at the alpine timberline revealed three di

43 n birch (Betula verrucosa) and spruce (Picea abies) GX.

44 d from the methanol extract of the trunks of Abies holophylla.

45 Norway spruce (Picea abies) is periodically attacked by the bark beetle Ips t

46 we found a diverse suite of conifers (Pinus, Abies, Juniperus, Picea, and Larix) strongly dominate th

47 lvatica) and coniferous Norway spruce (Picea abies Karst), planted in the same soil.

48 (Pinus sylvestris L.), Norway spruce (Picea abies L.), Siberian larch (Larix sibirica Ledeb.), silve

49 zation in microcosm systems containing Picea abies or Pinus sylvestris seedlings and each saprotrophi

50 ation of the gymnosperm Norway spruce (Picea abies, Pa) ESP.

51 ctomycorrhizal (EcM) and fine roots of Picea abies, Pinus sylvestris and Betula pendula were evaluate

52 ch was found in low frequency in the four P. abies populations that we studied.

53 of the apical-basal embryonic pattern in P. abies proceeds through the establishment of three major

54 In this study on Picea abies, refilling was monitored during winter and spring

55 ree coniferous species (Norway spruce [Picea abies], Scots pine [Pinus sylvestris], and silver fir [A

56 and nutrient uptake by Norway spruce (Picea abies) seedlings with fast- and slow-growing phenotypes.

57 orella trichopoda, with sequences from Picea abies, Selaginella moellendorffii and Physcomitrella pat

58 European tree species, Norway spruce (Picea abies), silver fir (Abies alba), and European beech (Fag

59 We used the P. abies somatic embryo system and a combination of reverse

60 We have used the gymnosperm, Picea abies, somatic embryogenesis model system to address thi

61 eaction is considered to be the precursor in Abies species of todomatuic acid, juvabione, and related

62 es in four 80 years old Norway spruce (Picea abies) stands (REFs) with those in four similar stands s

63 of these timbers were spruce (Picea) or fir (Abies) that were hand-carried from isolated mountaintops

64 rity of these modules are conserved in Picea abies The high spatial resolution of our data enabled id

65 onally characterized in Norway spruce (Picea abies), the most widespread and economically important c

66 that the resistance of Norway spruce (Picea abies) to Heterobasidion annosum s.l., a pathogenic basi

67 Norway spruce (Picea abies) trees (approximately 16 m high) of a single clone

68 forming cell culture of Norway spruce (Picea abies) was used as a research model.