ライフサイエンスコーパス: Pinus

1 distinct from, parasites of other species of Pinus.

2 genus often correlating with subdivisions of Pinus.

3 igh efficiency and specificity for the genus Pinus.

4 r sets amplified in four species of subgenus Pinus, 49% in one species of subgenus Strobus, and 22% i

5 gging, we found a diverse suite of conifers (Pinus, Abies, Juniperus, Picea, and Larix) strongly domi

6 trient depletion after a heavy mast event in Pinus albicaulis.

7 six pedigrees, representing two subgenera of Pinus and a distant member of the Pinaceae, Douglas-fir

8 is also conserved in two other gymnosperms, Pinus and Picea.

9 derosae) is a significant mortality agent of Pinus, and climate-driven range expansion is occurring.

10 pines from western North America: knobcone (Pinus attenuata Lemm.), Monterey (P. radiata D. Don), an

11 se (Adh) gene family is much more complex in Pinus banksiana than in angio-sperms, with at least seve

12 -intensity crown fire in a jack pine forest (Pinus banksiana) and carried out a detailed pre- and pos

13 cing, we discovered 11 diTPS from jack pine (Pinus banksiana) and lodgepole pine (Pinus contorta).

14 gepole pine (Pinus contorta), and jack pine (Pinus banksiana), and compared their activities with tho

15 is study, the infestation of whitebark pine, Pinus bungean, with B. xylophilus led to a significant i

16 is Mill., Pinus pinea L., Pinus pinaster and Pinus canariensis) grown in North Algeria were determine

17 As Pinus, Castanopsis, Gironniera, Rutaceae, Helicia, Randi

18 r relations were monitored for 15 months for Pinus cembroides and Quercus potosina tree species in a

19 Pinus chiapensis (Pinaceae) is a large conifer, endemic

20 cture within populations of two varieties of Pinus clausa.

21 ange of xylem pressures (Px) in the conifers Pinus contorta and Juniperus scopulorum.

22 t 70 km(2) of Rocky Mountain lodgepole pine (Pinus contorta latifolia) forest in southern Idaho, USA.

23 tive trait in Rocky Mountain lodgepole pine (Pinus contorta subsp. latifolia), a conifer that dominat

24 e 1980s as part of five disparate studies of Pinus contorta var.

25 beetle infested and healthy lodgepole pine (Pinus contorta var. latifolia) trees and ii.) from sites

26 he primary beetle host tree [lodgepole pine (Pinus contorta var. latifolia)] was not directly affecte

27 cent bark beetle outbreak in lodgepole pine (Pinus contorta) forests of western Canada to test whethe

28 aused extensive mortality of lodgepole pine (Pinus contorta) in forests of Colorado and Wyoming; it i

29 ed in two gymnosperms (Picea engelmannii and Pinus contorta) that experienced lethal water stress in

30 nifer species, Sitka spruce, lodgepole pine (Pinus contorta), and jack pine (Pinus banksiana), and co

31 k pine (Pinus banksiana) and lodgepole pine (Pinus contorta).

32 Pinus defenses in recently invaded areas, including high

33 ned the time to drought-induced mortality in Pinus edulis (pinon shortened pine) trees by nearly a th

34 draulics, gas exchange and carbon storage in Pinus edulis and Juniperus monosperma, two tree species

35 t where earlier drought-induced mortality of Pinus edulis at elevated temperatures was associated wit

36 onships with a die-off event of pinyon pine (Pinus edulis Engelm.) in southwestern North America duri

37 s from arid environments (Pinus longaeva and Pinus edulis in the US Southwest) as well as from wetter

38 se experiments of a foundation tree species (Pinus edulis) and its mutualistic ectomycorrhizal fungal

39 ion manipulation experiment in a pinon pine (Pinus edulis) and juniper (Juniperus monosperma) ecosyst

40 hanisms, and mortality of mature pinon pine (Pinus edulis) and one-seed juniper (Juniperus monosperma

41 duced shoot and needle growth in pinon pine (Pinus edulis) by >/=39%, while juniper (Juniperus monosp

42 Widespread pinon (Pinus edulis) mortality occurred across the southwestern

43 90% of the dominant, overstory tree species (Pinus edulis, a pinon) died.

44 physiology of a pinon pine-juniper woodland (Pinus edulis-Juniperus monosperma) that experienced mort

45 ll manipulation experiment in pinon-juniper (Pinus edulis-Juniperus monosperma) woodland using mixed

46 suitable for analysis of the related species Pinus elliottii Engelm.

47 ntitative trait loci (QTLs) in a (P. taeda x Pinus elliottii) x P. elliottii pseudo-backcross of 345

48 tosa, affects the growth of the target trees Pinus elliottii, Schima superba, Castanopsis fissa, and

49 tris, Brassica oleracea, Pennisetum glaucum, Pinus elliottii, Selaginella apoda, Vicia faba and Vicia

50 Comparative analysis of P450s in the Pinus expressed sequence tag collections has identified

51 consistent association between limber pine (Pinus flexilis) and potential N2 -fixing acetic acid bac

52 lated microclimatic factors for limber pine (Pinus flexilis) seedlings growing in a heating x waterin

53 e flow in a long-lived conifer, limber pine (Pinus flexilis).

54 racteristics of seeds of some pinus species (Pinus halepensis Mill., Pinus pinea L., Pinus pinaster a

55 ae Hopkins) are aggressive insects attacking Pinus host trees.

56 ted pine species (Pinus massoniana Lamb. and Pinus hwangshanensis Hisa) from Southeast China.

57 ka, the total cover of alder and dwarf pine (Pinus) increased 6.1% within one ecotone and was little

58 Fossil records indicate that the genus Pinus L. split into two subgenera by the Late Cretaceous

59 Lemmon is less well documented than subgenus Pinus L., especially in eastern Asia.

60 ned from a band visible in an agarose gel of Pinus lambertiana (sugar pine) genomic DNA is present in

61 The diploid genome of sugar pine (Pinus lambertiana Dougl.) has a highly repetitive, 31 bi

62 the noninvaded soils receiving recalcitrant Pinus litter had a similar abundance of plant biomarkers

63 l depth despite receiving similar amounts of Pinus litter.

64 arison with C3 trees from arid environments (Pinus longaeva and Pinus edulis in the US Southwest) as

65 the modern unprecedented level of growth for Pinus longaeva at these sites.

66 two long-lived species, GB bristlecone pine (Pinus longaeva) and foxtail pine (P. balfouriana), are u

67 Great Basin bristlecone pine (Pinus longaeva) at 3 sites in western North America near

68 00 and 5,062 years for Lomatia tasmanica and Pinus longaeva, respectively.

69 In this paper, Pinus maomingensis sp.nov. is established based on a com

70 era, Theobroma cacao, Camellia sinensis, and Pinus massoniana induced a significant increase in modul

71 genome of two closely related pine species (Pinus massoniana Lamb. and Pinus hwangshanensis Hisa) fr

72 of four native subtropical tree species in a Pinus massoniana plantation in southern China and found

73 e we report that seven distinct parasites of Pinus monticola do not occur as endophytes.

74 e, PmAMP1, isolated from western white pine (Pinus monticola), in providing canola with resistance ag

75 hanges in xylem sap gamma in Picea abies and Pinus mugo growing at the alpine timberline.

76 Pine trees (Pinus mugo in Slovakia and Pinus sylvestris in Norway) w

77 y 120 kb plastomes from eight species (seven Pinus, one Picea) in 35 reactions.

78 in the mixture of cultural medium and pine (Pinus palustris) litter-derived TA-DOMs (50 degrees C, 2

79 were assessed in a 25-yr-old longleaf pine (Pinus palustris) plantation where C flow was manipulated

80 le field study at 36 sites in longleaf pine (Pinus palustris) woodlands, we examined whether historic

81 l CO2 efflux for over 1 yr in longleaf pine (Pinus palustris), a species that has large reserves of s

82 ression of individual Lhcb mRNAs in the pine Pinus palustris, we have prepared sequence-specific cDNA

83 (25 years), and an estimated divergence from Pinus pinaster Ait. are used, the effective population s

84 s tested in 2D using data from Maritime pine Pinus pinaster Ait. structural roots as input.

85 ies (Pinus halepensis Mill., Pinus pinea L., Pinus pinaster and Pinus canariensis) grown in North Alg

86 of rice husks, Eucalyptus globulus wood and Pinus pinaster wood (containing arabinoxylan, acetylated

87 s robur, Populus tremula x Populus alba, and Pinus pinaster).

88 ore symbiotic structure differentiation with Pinus pinaster.

89 some pinus species (Pinus halepensis Mill., Pinus pinea L., Pinus pinaster and Pinus canariensis) gr

90 assembly methods, using previously published Pinus plastomes as surrogate references.

91 dy area may benefit from using plant taxa of Pinus, Poaceae, Lonicera, Casuarina, Trema and Quercus.

92 Using detritus from Pinus ponderosa and Abies concolor (dominant species in

93 Using a 40-y-old Pinus ponderosa genetic experiment, we provide rare evid

94 individuals in four disjunct populations of Pinus ponderosa that were initially established by long-

95 of a widespread gymnosperm (ponderosa pine - Pinus ponderosa) and angiosperm (trembling aspen - Popul

96 covariance measurements in a ponderosa pine (Pinus ponderosa)-dominated ecosystem in northern Arizona

97 s in a natural population of ponderosa pine (Pinus ponderosa, Laws).

98 Focusing on Eucalyptus, Pinus, Populus and Pseudotsuga - genera that represent d

99 Pinus radiata (Pinaceae) was found to exhibit ABA-driven

100 hyltransferase (CCoAOMT) was isolated from a Pinus radiata cDNA library derived from differentiating

101 ies drawn from a sample of the population of Pinus radiata introduced to Spain in the mid-19th centur

102 Using a transformable Pinus radiata tracheary element (TE) system as an experi

103 ed gene cinnamoyl-CoA reductase (CCR) in the Pinus radiata tracheary element (TE) system impacted bot

104 fication process in Arabidopsis thaliana and Pinus radiata under various feeding regimens.

105 (EGases) were isolated from a radiata pine (Pinus radiata) cDNA library prepared from immature femal

106 A pine (Pinus radiata) male cone-specific promoter, PrMC2, was u

107 We studied three species: Pinus radiata, Pinus sylvestris, and Cedrus libani.

108 hyma cells in normal and compression wood of Pinus radiata, was examined to determine the relationshi

109 ur species (Acer saccharum, Drypetes glauca, Pinus resinosa, and Thuja plicata) from four sites that

110 YB mRNA cleavage product guided by miR828 in Pinus resinosa.

111 zal interaction between Laccaria bicolor and Pinus resinosa.

112 he gene for MBO synthase was identified from Pinus sabiniana, and the protein encoded was functionall

113 Pinus seed's oil physicochemical properties show acid va

114 tree-ring width chronology of Siberian pine (Pinus sibirica Du Tour) growing at timberline (2450 mete

115 on water balance derived from Siberian pine (Pinus sibirica) trees in central Mongolia.

116 sheaths and bulbous bases are recognized as Pinus sp. and also represent Pinus subgenus Strobus.

117 icochemical characteristics of seeds of some pinus species (Pinus halepensis Mill., Pinus pinea L., P

118 nses against insects and fungal pathogens in Pinus species, increasing current knowledge regarding in

119 esponses against WPBR and insects in related Pinus species, suggesting that MeJA may be used to impro

120 Furthermore, we found no evidence that Pinus spp. synthesize 4-Cl-IAA in seeds, contrary to a p

121 ed real time PCR method for the detection of Pinus spp. was set up.

122 n acids (DRAs) are major components of pine (Pinus spp.) oleoresin.

123 a 22% higher litter input, P. lobata-invaded Pinus stands exhibited a 28% decrease in soil C and a tw

124 ving constitutive resin canal development in Pinus stems may enhance the capacity to synthesize terpe

125 ves, the key mechanism allowing invasion for Pinus strobus into nitrogen limited grasslands was its h

126 The defoliation of the eastern white pine (Pinus strobus) across the northeastern United States is

127 is and cold hardening in Eastern white pine (Pinus strobus).

128 e recognized as Pinus sp. and also represent Pinus subgenus Strobus.

129 This species is attributed to genus Pinus, subgenus Strobus, section Quinquefoliae Duhamel,

130 rrhizal (EcM) and fine roots of Picea abies, Pinus sylvestris and Betula pendula were evaluated along

131 We focus on Pinus sylvestris and Juniperus communis, assessing their

132 s tested using (14)CO2 supplied to shoots of Pinus sylvestris ectomycorrhizal with the widespread fun

133 R data from a 36-tree isolated population of Pinus sylvestris from the Meseta region of Spain, for wh

134 Pine trees (Pinus mugo in Slovakia and Pinus sylvestris in Norway) were chosen for sampling in

135 mposition and quantity of VOC emissions from Pinus sylvestris L. saplings.

136 We selected Scots pine (Pinus sylvestris L.) as a model species to explore growt

137 ere analysed from 15 seminatural Scots pine (Pinus sylvestris L.) forests.

138 s: a large noninbred pedigree of Scots pine (Pinus sylvestris L.) that includes additive and dominanc

139 Scots pine (Pinus sylvestris L.) wood is desired in woodworking indu

140 d 5-species mixtures composed of Scots pine (Pinus sylvestris L.), Norway spruce (Picea abies L.), Si

141 microcosm systems containing Picea abies or Pinus sylvestris seedlings and each saprotrophic fungus.

142 A cell-coupling analysis for Pinus sylvestris showed high symplasmic coupling along t

143 land; and SwedFACE proposed in a hemiboreal, Pinus sylvestris stand in Sweden.

144 x 2-cm(3) (800-cm(3)) slices of Scots pine (Pinus sylvestris) forest soil and divided each into 100

145 heir biomass distribution across Scots pine (Pinus sylvestris) populations both along a 2000-km latit

146 Microcosms containing Scots pine (Pinus sylvestris) seedlings colonized by different ECM f

147 Roots of Scots pine (Pinus sylvestris) were collected from sites between 300

148 ted species: birch (Betula verrucosa), pine (Pinus sylvestris), and ryegrass (Lolium perenne).

149 n ectomycorrhizal symbiosis with Scots pine (Pinus sylvestris), is able to oxidize a substantial amou

150 adaptation to the populations of Scots pine (Pinus sylvestris).

151 We studied three species: Pinus radiata, Pinus sylvestris, and Cedrus libani.

152 about situations, exemplified by Scots pine, Pinus sylvestris, and its fungal pathogen Crumenulopsis

153 ula pendula, Larix decidua, Picea abies, and Pinus sylvestris; and alien species-Pseudotsuga menziesi

154 species (silver fir, Abies alba; Scots pine, Pinus sylvestris; and mountain pine, Pinus uncinata) in

155 es (Norway spruce [Picea abies], Scots pine [Pinus sylvestris], and silver fir [Abies alba]).

156 ases and associated mesophication in Quercus-Pinus systems were delayed until mid 20th century fire s

157 and 6 yr of nitrogen (N) fertilization in a Pinus taeda (loblolly pine) forest.

158 disease-resistance properties, measured in a Pinus taeda (loblolly pine) training population of 951 i

159 Needles and branches of Pinus taeda (Loblolly pine) were sprayed with the pestic

160 m a library constructed from differentiating Pinus taeda (loblolly pine) xylem RNA.

161 15NH4Cl, 15N-Gln, and 15N-Glu) in lignifying Pinus taeda cell cultures was investigated, using a comb

162 profiling of the phenylpropanoid pathway in Pinus taeda cell suspension cultures was carried out usi

163 lization on EMM production and turnover in a Pinus taeda forest.

164 atural and tracer nitrogen (N) isotopes in a Pinus taeda free air CO(2) enrichment (FACE) experiment

165 atural and tracer nitrogen (N) isotopes in a Pinus taeda free air CO(2) enrichment (FACE) experiment

166 ee environments in a complex pedigree of 520 Pinus taeda individuals (CCLONES).

167 rigin of early 20th century introductions of Pinus taeda into Zimbabwe is possible given microsatelli

168 ortant plant species, such as loblolly pine (Pinus taeda L).

169 Pinus taeda L. (loblolly pine) and Arabidopsis thaliana

170 Molecular dissection of a Pinus taeda L. selfed pedigree detected a chromosomal re

171 at a FACE site where leaf area index (L) of Pinus taeda L. was altered through nitrogen fertilizatio

172 homologous linkage groups in loblolly pine (Pinus taeda L.) and Douglas fir (Pseudotsuga menziesii [

173 r deficit was isolated from a loblolly pine (Pinus taeda L.) cDNA library and characterized.

174 ag polymorphisms (ESTPs) from loblolly pine (Pinus taeda L.) for this function.

175 lived, outcrossing gymnosperm loblolly pine (Pinus taeda L.) from a survey of single nucleotide polym

176 We have discovered a mutant loblolly pine (Pinus taeda L.) in which expression of the gene encoding

177 Loblolly pine (Pinus taeda L.) is the most widely planted tree species

178 Loblolly pine trees (Pinus taeda L.) occupy more than 20% of the forested are

179 uum f. sp fusiforme infecting loblolly pine (Pinus taeda L.) over much of this host's natural range.

180 lignin is formed in a mutant loblolly pine (Pinus taeda L.) severely depleted in cinnamyl alcohol de

181 A consensus map for loblolly pine (Pinus taeda L.) was constructed from the integration of

182 ligase (4CL; EC 6.2.1.12) in loblolly pine (Pinus taeda L.) were cloned.

183 ide oxidoreductases (PORs) in loblolly pine (Pinus taeda L.) were examined.

184 For instance, loblolly pine (Pinus taeda L.), an ecologically and economically import

185 synthase gene, PtaACS1, from loblolly pine (Pinus taeda L.), an important commercial forest tree spe

186 ty loci in a selfed family of loblolly pine (Pinus taeda L.), using data from AFLP markers from an es

187 y across the natural range of loblolly pine (Pinus taeda L.).

188 ygotic and somatic embryos of loblolly pine (Pinus taeda L.).

189 accession number AF101785) in loblolly pine (Pinus taeda L.).

190 g xylem and in mature wood of loblolly pine (Pinus taeda L.).

191 tained from immature xylem of loblolly pine (Pinus taeda L.).

192 ctured breeding population of loblolly pine (Pinus taeda L.).

193 icated full-sibling family of loblolly pine (Pinus taeda L.).

194 ndidate genes for drought-stress response in Pinus taeda L., an important tree crop.

195 Loblolly pine, Pinus taeda L., is one of the most widely planted, comme

196 This MYB family member, Pinus taeda MYB1 (PtMYB1), was most abundantly expressed

197 This MYB, Pinus taeda MYB4 (PtMYB4), is expressed in cells undergo

198 ee cohorts of selfed offspring from a single Pinus taeda parent were genotyped for nuclear microsatel

199 sis thaliana, is most closely related to the Pinus taeda phenylpropenal double bond reductase, involv

200 us, the response of understory vegetation in Pinus taeda plantation at the Duke Forest FACE site afte

201 luated the utility of genomic selection in a Pinus taeda population of c.

202 we show that range expansions of introduced Pinus taeda result from an interaction between genetic p

203 owever, mCG-enriched genes in the gymnosperm Pinus taeda shared some similarities with gbM genes in A

204 endophytic fungi associated with needles of Pinus taeda trees across regional scales in the absence

205 dventitious root formation in loblolly pine (Pinus taeda) after treatment with the exogenous auxin in

206 abolites measured in a single loblolly pine (Pinus taeda) association population.

207 ranscripts of Arabidopsis and loblolly pine (Pinus taeda) CslA genes display tissue-specific expressi

208 experimental forest plots of loblolly pine (Pinus taeda) exposed to high CO2 concentrations, nearly

209 nd nitrogen (N) turnover in a loblolly pine (Pinus taeda) forest exposed to elevated CO(2) by measuri

210 vity and water use of planted loblolly pine (Pinus taeda) growing across the southeastern United Stat

211 Only two CYP720B members, loblolly pine (Pinus taeda) PtCYP720B1 and Sitka spruce (Picea sitchens

212 approach to identify genes in loblolly pine (Pinus taeda) that are associated with resistance to pitc

213 hin a pedigreed population of loblolly pine (Pinus taeda) that was clonally replicated at three sites

214 ctive response of 19-year-old loblolly pine (Pinus taeda) to 4 years of carbon dioxide (CO2) enrichme

215 rstanding of the responses of loblolly pine (Pinus taeda) to drought stress.

216 mRNA from lignifying xylem of loblolly pine (Pinus taeda) trunk wood.

217 t here the first cloning of a loblolly pine (Pinus taeda) xylem cDNA encoding a multifunctional enzym

218 that is abundant in immature loblolly pine (Pinus taeda) zygotic and somatic embryos, but is undetec

219 Loblolly pine (Pinus taeda), in contrast, possesses a single 4CL protei

220 26 miRNAs from stem xylem of loblolly pine (Pinus taeda), which belong to four conserved and seven l

221 s containing 2,178 cDNAs from loblolly pine (Pinus taeda).

222 way spruce (Picea abies), and loblolly pine (Pinus taeda).

223 Analysis of full-length AAH cDNAs from Pinus taeda, Physcomitrella patens, and Chlamydomonas re

224 enzylic ether reductase from the gymnosperm, Pinus taeda, was cloned, with the recombinant protein he

225 ants, selection is found to be quite weak in Pinus thunbergii and the angiosperms but there is eviden

226 in the light in cotyledons of the black pine Pinus thunbergii.

227 riation present in the chloroplast genome of Pinus torreyana (Parry ex Carriere) that may previously

228 s pine, Pinus sylvestris; and mountain pine, Pinus uncinata) in mountainous areas of NE Spain.

229 factor (CaPF1) in transgenic Virginia pine (Pinus virginiana Mill.) confers tolerance to heavy metal

230 genomic DNA is present in both subgenera of Pinus with at least 10(4) copies/genome.

231 also suggest that IFG continued to evolve in Pinus with restriction fragment length polymorphism (RFL