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1 h cellulose surfaces in Norway spruce (Picea abies).
2 aptation of the conifer Norway spruce (Picea abies).
3 ent of sustained NPQ in Norway spruce (Picea abies).
4 resence of two PaLAR3 allelic lineages in P. abies.
5 sely related to linalool synthase from Picea abies.
6 mpacts on the belowground productivity of P. abies.
7 cDNAs for peptidoglycan biosynthesis from P. abies.
8 on optimized longifolene synthase from Picea abies.
9 leaf carbon dynamics in Norway spruce (Picea abies), a dominant northern forest species, to improve p
10         We aimed to show whether silver fir (Abies alba Mill.) can be an appropriate host partner for
11                         Although Silver fir (Abies alba) and Douglas fir (Pseudotsuga menziesii) have
12                 Using needles of silver fir (Abies alba) seedlings as test subjects, we show that the
13  assembly of the closely related Silver fir (Abies alba) species and a de novo assembly of low-copy r
14 es, Norway spruce (Picea abies), silver fir (Abies alba), and European beech (Fagus sylvatica).
15  "winners"-mostly late-successional species: Abies alba, Fagus sylvatica, Fraxinus excelsior, Quercus
16 f the climate change and aging hypotheses in Abies alba, Fagus sylvatica, Larix decidua, Picea abies,
17 w classification of three botanical origins (Abies alba, Quercus frainetto, Quercus ilex).
18 ate of three major tree species (silver fir, Abies alba; Scots pine, Pinus sylvestris; and mountain p
19 ots pine [Pinus sylvestris], and silver fir [Abies alba]).
20 nus banksiana, Pinus contorta, Larix lyalli, Abies amabilis, and Abies lasiocarpa.
21  at 50% loss of hydraulic conductivity in P. abies and P. mugo was -3.35 and -3.86 MPa at gamma of 74
22 seasonal changes in xylem sap gamma in Picea abies and Pinus mugo growing at the alpine timberline.
23 NA population from the conifer spruce (Picea abies) and compared the results with those of a range of
24 ncluding the gymnosperm Norway spruce (Picea abies) and the angiosperms rice (Oryza sativa), tobacco
25  spruce (Picea glauca), Norway spruce (Picea abies), and loblolly pine (Pinus taeda).
26 s, we isolated KCBP from a gymnosperm, Picea abies, and a green alga, Stichococcus bacillaris.
27 ords of montane conifers (Tsuga, Podocarpus, Abies, and Picea) as a new paleoaltimetry to construct t
28 pecies: Betula pendula, Larix decidua, Picea abies, and Pinus sylvestris; and alien species-Pseudotsu
29 nt tree species such as Norway spruce (Picea abies) are required, if the frequency and intensity of s
30 ng juvenile period, for Norway spruce (Picea abies) around 20 to 25 years, before developing male and
31 e sampled the roots of Betula papyrifera and Abies balsamea saplings growing in the B4Warmed (Boreal
32 ent of the aromatic oleoresin of balsam fir (Abies balsamea) and serves as a valuable bioproduct mate
33 opulus spp.) or to biotic disturbances (e.g. Abies balsamea).
34 wave-regenerating populations of balsam fir, Abies balsamea, in order to estimate Ne/N.
35 cer saccharum to severe growth reductions in Abies balsamea, Picea glauca and Pinus strobus.
36 o the lignin polymer in Norway spruce (Picea abies) bark.
37 birch (Betula pendula), Norway spruce (Picea abies), bird cherry (Prunus padus), mountain ash (Sorbus
38 tified in the genome of the gymnosperm Picea abies but these could be pseudogenes or encode proteins
39  relative regulation in Norway spruce (Picea abies) clones.
40      Using detritus from Pinus ponderosa and Abies concolor (dominant species in forests in the weste
41 crobial taxa in the functioning of the Picea abies-dominated coniferous forest soil in two contrastin
42 udates from mature Fagus sylvatica and Picea abies exposed to experimental drought, and combining abo
43 genetic studies have suggested a role for P. abies FLOWERING LOCUS T/TERMINAL FLOWER1-Like2 (PaFTL2)
44                         Norway spruce (Picea abies) forests suffer periodic fatal attacks by the bark
45 a(13) C and delta(18) O series of Smith fir (Abies georgei var. smithii) on the southeastern Tibetan
46                    Abietadiene synthase from Abies grandis (AgAS) is a model system for diterpene syn
47 (15)), and abietadiene synthase (C(20)) from Abies grandis and taxadiene synthase (C(20)) from Taxus
48                                   Grand fir (Abies grandis Lindl.) has been developed as a model syst
49  geranyl diphosphate synthase from the plant Abies grandis was expressed to optimize the limonene bio
50 hosphate synthases from Taxus canadensis and Abies grandis yielded a functional hybrid heterodimer th
51                                   Grand fir (Abies grandis) has been developed as a model system for
52                                   Grand fir (Abies grandis) has been developed as a model system for
53         The oleoresin secreted by grand fir (Abies grandis) is composed of resin acids derived largel
54 ucible sesquiterpene synthases of grand fir (Abies grandis), and the olefin product of this cyclizati
55 und-induced oleoresin secreted by grand fir (Abies grandis), is synthesized by the cyclization of ger
56 tep of resin acid biosynthesis in grand fir (Abies grandis).
57 ield experiments during late winter on Picea abies growing at the alpine timberline revealed three di
58 n birch (Betula verrucosa) and spruce (Picea abies) GX.
59 d from the methanol extract of the trunks of Abies holophylla.
60  typographus) attacking Norway spruce (Picea abies) hydrolyze phenolic glucosides to their correspond
61 migration history of the Norway spruce Picea abies in Quaternary has affected its host-associated her
62                         Norway spruce (Picea abies) is periodically attacked by the bark beetle Ips t
63 we found a diverse suite of conifers (Pinus, Abies, Juniperus, Picea, and Larix) strongly dominate th
64 f dissimilarity was recorded between PCV and Abies-Juniperus-Picea (AJP) communities.
65 lvatica) and coniferous Norway spruce (Picea abies Karst), planted in the same soil.
66 ted genetic material of Norway spruce (Picea abies L.
67 tion in dying adults of Norway spruce (Picea abies L.) during the progression of the record-breaking
68  (Pinus sylvestris L.), Norway spruce (Picea abies L.), Siberian larch (Larix sibirica Ledeb.), silve
69 r of hourly stem radial increment from Picea abies (L.) Karst.
70  contorta, Larix lyalli, Abies amabilis, and Abies lasiocarpa.
71 Pinus sylvestris L) and Norway spruce (Picea abies) needles display strong O(2) consumption even in t
72  were used to identify SNPs in Nordmann fir (Abies nordmanniana), a species previously lacking genomi
73 f Fagus sylvatica (European beech) and Picea abies (Norway spruce) by means of a 4-yr-long throughfal
74 trees exuded 1.0% (F. sylvatica) to 2.5% (P. abies) of net C into the rhizosphere, increasing the pro
75 zation in microcosm systems containing Picea abies or Pinus sylvestris seedlings and each saprotrophi
76           GFP fusion proteins with either P. abies (Pa)MurE or PaPBP were detected in chloroplasts.
77 ation of the gymnosperm Norway spruce (Picea abies, Pa) ESP.
78 er genomes sequenced and assembled for Picea abies, Picea glauca, Pinus taeda, Pinus lambertiana, and
79 ctomycorrhizal (EcM) and fine roots of Picea abies, Pinus sylvestris and Betula pendula were evaluate
80  alba, Fagus sylvatica, Larix decidua, Picea abies, Pinus sylvestris, Quercus petraea, and Quercus ro
81 ch was found in low frequency in the four P. abies populations that we studied.
82  of the apical-basal embryonic pattern in P. abies proceeds through the establishment of three major
83                       In this study on Picea abies, refilling was monitored during winter and spring
84                             Water-limited P. abies released two-thirds of its exudate C into the surf
85 hfall-exclusion prolonged the lifespan of P. abies roots but did not change the lifespan of F. sylvat
86 s (SM)) in well-watered Norway spruce (Picea abies) saplings.
87 ree coniferous species (Norway spruce [Picea abies], Scots pine [Pinus sylvestris], and silver fir [A
88  and nutrient uptake by Norway spruce (Picea abies) seedlings with fast- and slow-growing phenotypes.
89 orella trichopoda, with sequences from Picea abies, Selaginella moellendorffii and Physcomitrella pat
90  European tree species, Norway spruce (Picea abies), silver fir (Abies alba), and European beech (Fag
91                               We used the P. abies somatic embryo system and a combination of reverse
92           We have used the gymnosperm, Picea abies, somatic embryogenesis model system to address thi
93 eaction is considered to be the precursor in Abies species of todomatuic acid, juvabione, and related
94 alayan birch Betula utilis and Himalayan fir Abies spectabilis, in KMD's preferred forests.
95                                    True fir (Abies spp.) are the most popular trees and account for t
96 es in four 80 years old Norway spruce (Picea abies) stands (REFs) with those in four similar stands s
97 of these timbers were spruce (Picea) or fir (Abies) that were hand-carried from isolated mountaintops
98 rity of these modules are conserved in Picea abies The high spatial resolution of our data enabled id
99 onally characterized in Norway spruce (Picea abies), the most widespread and economically important c
100  that the resistance of Norway spruce (Picea abies) to Heterobasidion annosum s.l., a pathogenic basi
101                         Norway spruce (Picea abies) trees (approximately 16 m high) of a single clone
102 nus-Cedrus-Viburnum (PCV) and Viburnum-Pinus-Abies (VPA) communities, and the highest index of dissim
103 forming cell culture of Norway spruce (Picea abies) was used as a research model.
104 wever, this reduction was not evident for P. abies when grown intermixed with F. sylvatica.
105 -facing slope) on the decomposition of Picea abies wood blocks and their microbiome over two years.

 
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