ライフサイエンスコーパス: moss

1 pika populations to consume high amounts of moss.

2 ell as to the especially challenging diet of moss.

3 liana and essential for stomata formation in moss.

4 niplanar to triplanar meristematic growth in moss.

5 auxin transport regulates morphogenesis in a moss.

6 t, NIH, and organized by Rich Maraia and Tom Moss.

7 roles for reproductive organ development in moss.

8 drial genomes from three green algae and one moss.

9 e bottom, partially decomposed, layer of the moss.

10 is the protein responsible for quenching in moss.

11 sponsible for dissipation in green algae and moss.

12 of microbiome community composition in peat mosses.

13 spheric N2 fixation associated with Sphagnum mosses.

14 ass compensated for the decrease in Sphagnum mosses.

15 emerging concept of evolutionary dynamism in mosses.

16 the branching pattern of the gametophyte in mosses.

17 icantly higher (p = 0.035) than in far-field moss (118 ng/g, n = 13), and increasing temporal trends

18 Average PAH concentrations in near-field moss (199 ng/g, n = 11) were significantly higher (p = 0

19 PAHs were measured in living Sphagnum moss (24 sites, n = 68), in sectioned peat cores (4 site

20 Addition of moss, a plant representative 200 million years diverged

21 Moss abundance, associated with ecosystem disturbances,

22 Forest type and leaf litter inputs regulate moss abundance, but how they control moss microbiomes an

23 tly, N + P has caused dramatically increased moss abundance, which influences nutrient dynamics.

24 Rates of moss accumulation are more than three times higher in th

25 n plants, including algae, lowland plants (a moss and a lycophyte), monocots, and eudicots.

26 s of angiosperms, and 15,726 of land plants (moss and angiosperms).

27 eir unit increased for combat arms and other MOSs and for units of any size but particularly for smal

28 th content representing the major liverwort, moss and hornwort clades.

29 nd cyclocitral oxime (earthy with patchouli, moss and leather notes).

30 urface roughness following treatment-induced moss and lichen mortality.

31 Structural analysis of mannans from moss and Selaginella showed they were composed of mannos

32 cted in increasing delta(15)N values in soil/moss and springtails with increasing seabird influence.

33 Although this network has diverged in the moss and the angiosperm lineages, our data demonstrate t

34 Here, using both moss and tobacco, we show that myosin VIII associates wi

35 ork acted in the last common ancestor of the mosses and angiosperms that existed sometime before 420

36 croalgae to bryophyta and pteridophyta, i.e. mosses and ferns, but interestingly not in higher plants

37 the multicellular diploid sporophyte in both mosses and flowering plants; however, the morphological

38 he nonvascular bryophyte groups (liverworts, mosses and hornworts), with moss sequences being most si

39 ent in multiple subclades within liverworts, mosses and hornworts, but these phyla were not ancestral

40 Mosses and hornworts, the most ancient extant lineages t

41 creased nitrogen concentrations in Antarctic mosses and lichens for their associated food web has har

42 librated large-scale phylogenies reveal that mosses and liverworts underwent bursts of diversificatio

43 uction of these characters was performed for mosses and liverworts using published phylogenies.

44 two of the three lineages of bryophytes, the mosses and liverworts, is steadily accumulating, the bio

45 , which lacks the NTD found in homologs from mosses and plants.

46 ge priming branching form diversification in mosses and provide a framework for mechanistic studies o

47 also control the development of rhizoids in mosses and root hairs in angiosperms [13, 14], these dat

48 ero-oligomeric CSCs evolved independently in mosses and seed plants and we propose the constructive n

49 e Cellulose Synthase (CESA) gene families of mosses and seed plants diversified independently, CESA k

50 en CSCs of this type evolved convergently in mosses and seed plants.

51 ce of stomata in the last common ancestor of mosses and vascular plants coincided with the origin of

52 GPP), often includes contributions from both mosses and vascular plants in boreal ecosystems.

53 of the florideophyte Chondrus crispus (Irish moss) and the annotation of the 9,606 genes.

54 tcoke was the major source of PAHs to living moss, and among three peat core the contribution to PAHs

55 , from a charophyte alga, a liverwort, and a moss, and functionally analyzed the channel-kinase inter

56 arvesting complexes (LHCs) of higher plants, moss, and green algae can undergo dynamic conformational

57 oleosin lineages: primitive (in green algae, mosses, and ferns), universal (U; all land plants), and

58 ation is observed in DT resurrection plants, mosses, and green algae most closely related to these Em

59 for 501 genes conserved in dicots, monocots, mosses, and green algae.

60 n all plants, including primitive plants and mosses, and in some fungi and bacteria.

61 These proteins are found in cyanobacteria, mosses, and microalgae, but have been lost in angiosperm

62 itochondrial DNA, acquired from green algae, mosses, and other angiosperms.

63 crusts) soil surface communities of lichens, mosses, and/or cyanobacteria comprise up to 70% of dryla

64 een PpSMF1 and PpSCRM1, which, together with moss-angiosperm gene complementations(6), suggests deep

65 Mosses are a highly diverse lineage of land plants, whos

66 ificance in the evolutionary history of peat mosses are discussed.

67 Mosses are the dominant plants in polar and boreal regio

68 Mosses are the most species-rich bryophyte lineage and t

69 entrations of each of these metals in the AB mosses are within a factor of 3 of "natural, background"

70 turase genes in angiosperms, lycophytes, and mosses arose by multiple shared and independent transfer

71 tion of angiosperms, ferns, gymnosperms, and mosses as well as various groups of animals during the C

72 soil microbial activity from a 150-year-old moss bank at the southern limit of significant plant gro

73 Here we use moss bank cores from a 600-km transect from Green Island

74 orroborated by many regional records showing moss bank initiation and decreased sea ice extent during

75 To our knowledge, while aerobic 'moss banks' have often been examined, waterlogged 'peatl

76 ionary intermediate Physcomitrella patens, a moss, both gene products are active.

77 Here we define the architectures of 175 mosses by the number of module classes, branching patter

78 For the same NDVI, moss can generate only about one-third of the GPP that v

79 green fluorescent protein-tagged kin14-VI in moss cells revealed fluorescent punctae that moved proce

80 artners that still support protein import in moss cells, but are orthogonal to the naturally occurrin

81 that concentrations were higher in soil and moss close to the bird cliff, compared to farther away.

82 Particle size was more variable in moss closer to industry.

83 viatica) and their respective habitats (soil/moss) collected underneath seabird cliffs.

84 by Warnstorfia fontinaliopsis, a wet-adapted moss commonly found in the Antarctic Peninsula.

85 erating the replacement of formerly dominant moss communities by vascular plants, and in increasing t

86 gous recombination over NHEJ pathways in the moss, contrary to the inverse situation in flowering pla

87 Mosses contribute substantially to biomass, but their im

88 munity states marked by dramatic declines in moss cover and increases in cyanobacteria cover, with mo

89 atabolism, and controls the synthesis of the moss cuticle, which prevents desiccation and organ fusio

90 involved in a tripartite symbiosis system of moss, cyanobacteria, and fungus.

91 d that isotope signatures of living sphagnum moss (Delta(199)Hg = -0.11 +/- 0.09 per thousand, Delta(

92 Support cells within the leaf midribs of mosses deposit cellulose-rich secondary cell walls, but

93 Furthermore, injection of moss-derived factor H reduced C3 deposition and increase

94 lycans, yielding approximately 1 mg purified moss-derived human factor H per liter of initial P. pate

95 re, we present the production of an improved moss-derived recombinant human factor H devoid of potent

96 by wildfire converted the low productivity, moss-dominated peatland to a non-carbon accumulating shr

97 surfaces lacking biocrusts, biocrust-forming mosses enhanced multiple functions related to C, N and P

98 Overall, the moss enzymes resembled their counterparts from seed plan

99 ole for the ancestral phenolic metabolism in moss erect growth and cuticle permeability, consistent w

100 were distinct 'hotspots' of mycelium in the moss/F1 layer.

101 G) aldolase, is widespread in cyanobacteria, moss, fern, algae, and plants and is even more common am

102 ns localize in a polar manner to the tips of moss filaments, revealing an unexpected relation between

103 ssible limitations in the use of terrestrial mosses for monitoring atmospheric pollution.

104 ion/dissolution under the skin in a dendrite/moss-free manner.

105 In comparison to contemporary Sphagnum moss from four bogs in rural locations of southern Germa

106 New Brunswick, the Pb concentrations in the mosses from AB are far lower.

107 Moss gametophores have modular development and each modu

108 Haploid moss gametophytes harbor distinct stem cell types, inclu

109 pendently in flowering plant sporophytes and moss gametophytes.

110 nitiation, leaf shape, and shoot tropisms in moss gametophytes.

111 Mosses grow slowly, but cold temperatures minimize decom

112 Moss growth and mass accumulation rates represent the ba

113 We developed a unique time series of past moss growth and soil microbial activity from a 150-year-

114 ding of climatic proxies and determinants of moss growth for contrasting continental and maritime Ant

115 The interplay between moss growth form, photosynthetic physiology, water statu

116 The regional sensitivity of moss growth to past temperature rises suggests that terr

117 This thiol switch is unique to mosses, gymnosperms, and angiosperms.

118 The ratio in mosses had an average value of 22 Bq mg(-1).

119 Moreover, pikas that feed on moss harboured microbial communities highly enriched in

120 lla patens by homologous recombination, this moss has been a premier model system to study evolutiona

121 Knock-outs of a putative moss homologue of the A. thaliana MS2 gene, which is hig

122 Yet, as the sister group to liverworts and mosses, hornworts are critical in understanding the evol

123 The concentrations of "heavy metals" in the mosses, however, are proportional to the concentration o

124 ironmental problems in the Arctic related to mosses in a changing climate, but the geographical range

125 ttiaceae) is one of the most abundant desert mosses in the world and thrives in an extreme environmen

126 Mosses incorporated 20 +/- 9% of total ecosystem GPP int

127 experimentally-induced stress in desiccated mosses, indicating that spectral imaging is an effective

128 Here we show that 1) entire moss individuals, dated by (14)C, survived through crypt

129 The molecular mechanisms by which perennial mosses interact with these fungal partners along their s

130 The lichen Cetraria islandica or Iceland Moss is commonly consumed as tea, food ingredients (e.g.

131 Finally, ALDH12 expression in maize and moss is downregulated in response to salt and drought st

132 In addition, we adopted moss kinesin-14 for efficient retrograde transport with

133 lower ALTs) were tree leaf area index (LAI), moss layer thickness and understory LAI in that order.

134 of magnetic properties reported for lichens, mosses, leaves, bark, trunk wood, insects, crustaceans,

135 se ecosystems, soil communities dominated by mosses, lichens and cyanobacteria (biocrusts) play a key

136 gical soil crusts (biocrusts)-communities of mosses, lichens, cyanobacteria, and heterotrophs living

137 lanar growth occurs progressively during the moss life cycle, and is thought to mirror evolution of t

138 ny sporophyte, the only diploid stage in the moss life cycle.

139 are ubiquitously expressed during the entire moss life cycle.

140 A new study reports that moss likely utilise this same mechanism, and thus suppor

141 ation of UAS homologs from avascular plants (mosses, liverwort, and hornwort), from streptophyte gree

142 e four major lineages of terrestrial plants (mosses, liverworts, hornworts, and vascular plants) is e

143 t availability, higher woody : foliar ratio, moss loss, and enhanced decomposition.

144 response to ABA and CO2 was found in several moss, lycophyte, and fern species.

145 scent vascular plants related to living club mosses (Lycophytes), ferns (Monilophytes), horsetails (E

146 ndependent gene duplications occurred within mosses, lycopods, ferns and seed plants, leading to dive

147 ify a set of candidate genes associated with moss male infertility.

148 uld be applied for authentication of Iceland Moss materials.

149 Nitrogen (N(2) )-fixing moss microbial communities play key roles in nitrogen cy

150 The moss microbiome and environmental conditions controlled

151 egulate moss abundance, but how they control moss microbiomes and N(2) -fixation remains understudied

152 cts of biocrust type (cyanobacteria, lichen, moss, mixed), soil texture (sand, loam, clay), and clima

153 Together, our results imply that the moss MKN2 protein can function in a broader developmenta

154 Conversely, the moss MS2 gene could not rescue the A. thaliana ms2 pheno

155 Despite this similarity, moss mutants were not complemented by vascular plant KNO

156 Mosses native to and transplanted into spruce stands sup

157 The average Se concentration in moss near industries (58 +/- 13 mug/kg; n = 75) was grea

158 In green algae, diatoms, and mosses, NPQ depends on the light-harvesting complex stre

159 Peat mosses of the genus Sphagnum play a major role in global

160 practices aimed at re-establishing Sphagnum moss on degraded peatlands could reduce costs and improv

161 elative positive effects of biocrust-forming mosses on multifunctionality compared with bare soil inc

162 positive effects exerted by biocrust-forming mosses on the abundance of soil bacteria and fungi.

163 n springtails and the concentrations in soil/moss, or with level of seabird influence.

164 sis of 142 species representing 29 of the 30 moss orders reveals that relative average rates of non-s

165 ses for the relationships and delineation of moss orders.

166 D, DIP, and Intact databases was queried for moss orthologs existing for both interacting partners.

167 ds of the rate of recent climate change, but moss peat banks contain an unrivalled temporal record of

168 at which ancient carbon stores laid down as moss peat over centuries or millennia are returned to th

169 n slowly-decomposing organic matter, such as moss peat.

170 evapotranspiration by 410% within a feather moss peatland by burning through the protective capping

171 Moss PEX11 functions in peroxisome division similar to P

172 phthous stomatitis, tongued tonsillitis with moss, pharyngitis, and submandibular lymphadenitis with

173 distinct eukaryotic kingdoms, including the moss Physcomitrella patens (Plantae), the brown alga Ect

174 phosphatase (FBPase), in both cases from the moss Physcomitrella patens (Pp).

175 We identified nine orthologs of FAAH in the moss Physcomitrella patens (PpFAAH1 to PpFAAH9) with ami

176 utative target genes of PHY signaling in the moss Physcomitrella patens and found light-regulated gen

177 minus-end-directed kinesin-14 motors in the moss Physcomitrella patens and found that none are proce

178 controlling caulonema differentiation in the moss Physcomitrella patens and root hair development in

179 In the moss Physcomitrella patens and the fern Adiantum capillu

180 and FAMA-like) and PpSCREAM1 (SCRM1) in the moss Physcomitrella patens are orthologous to transcript

181 cally in the polarized expansion zone of the moss Physcomitrella patens caulonemal cells through the

182 Here we show that the moss Physcomitrella patens Cold-Shock Domain Protein 1 (

183 The moss Physcomitrella patens contains the highly conserved

184 We find that an IRX10 homolog from the moss Physcomitrella patens displays robust activity, and

185 c analyses also show that phy mutants of the moss Physcomitrella patens exhibit abnormal cuticle comp

186 , we use molecular genetics to show that the moss Physcomitrella patens has conserved homologues of a

187 The moss Physcomitrella patens has rosette CSCs and seven CE

188 The moss Physcomitrella patens has six PEX11 isoforms which

189 Early land plants like moss Physcomitrella patens have developed remarkable dro

190 tions in nonvascular land plants such as the moss Physcomitrella patens Here, we provide evidence for

191 ghly efficient homologous recombination, the moss Physcomitrella patens is a model organism particula

192 The moss Physcomitrella patens is an important model organis

193 Overexpressing duckweed UAS in the moss Physcomitrella patens led to an increase in the amo

194 ogs even among early land plants such as the moss Physcomitrella patens or the clubmoss Selaginella m

195 In planta as in the moss Physcomitrella patens protoplasts, the presence of

196 ical, and functional characterization of the moss Physcomitrella patens PTEN gene family.

197 emonstrate that ARABIDILLO homologues in the moss Physcomitrella patens regulate a previously undisco

198 PAT function in Arabidopsis thaliana and the moss Physcomitrella patens results in a shared defect in

199 independently, CESA knockout analysis in the moss Physcomitrella patens revealed parallels with Arabi

200 We aimed to localize DEK1 in the moss Physcomitrella patens to decipher its function duri

201 und that treating gametophytic shoots of the moss Physcomitrella patens with exogenous auxins and aux

202 In the kaurene synthase from the moss Physcomitrella patens, 16-alpha-hydroxy-ent-kaurane

203 However, in the early divergent moss Physcomitrella patens, 3D growth is preceded by an

204 The moss Physcomitrella patens, a model for early terrestria

205 zed thylakoid protein phosphorylation in the moss Physcomitrella patens, assessing the thylakoid phos

206 ng land plant lineage, as exemplified by the moss Physcomitrella patens, auxin transport by PIN trans

207 raction analysis, we demonstrate that in the moss Physcomitrella patens, phytochrome4 physically inte

208 suggests that this macro2 domain gene in the moss Physcomitrella patens, PpMACRO2, is important in ep

209 everal members of MET1 and CMT families, the moss Physcomitrella patens, serving as a model for early

210 GRL1) for photosynthetic performances in the moss Physcomitrella patens, we generated a pgrl1 knockou

211 Using small RNA-sequencing (RNA-seq) of the moss Physcomitrella patens, we identified 1090 loci that

212 In the moss Physcomitrella patens, we show that phytochrome 4 (

213 orthologs from Arabidopsis thaliana and the moss Physcomitrella patens, which represent a distinct c

214 crotubule overlap in the phragmoplast of the moss Physcomitrella patens.

215 was complemented by the PpMKN2 gene from the moss Physcomitrella patens.

216 ric G-proteins from a nonvascular plant, the moss Physcomitrella patens.

217 2016) explore the role of the pathway in the moss Physcomitrella patens.

218 lar axillary hairs on the gametophyte of the moss Physcomitrella patens.

219 cooption of the TAS3 tasiRNA pathway in the moss Physcomitrella patens.

220 rom multiplanar gametophore bud cells in the moss Physcomitrella patens.

221 lopmental regulation of DEK1 activity in the moss Physcomitrella patens.

222 ion of all known prenylation subunits in the moss Physcomitrella patens.

223 equencing to obtain HS transcriptomes in the moss Physcomitrella patens.

224 f the earliest plants on land, the Bryophyte moss Physcomitrella patens.

225 e of RAD51 and its antagonist, RTEL1, in the moss Physcomitrella patens.

226 me respects different from that of the model moss Physcomitrella patens.

227 otypic male fertility difference between two moss (Physcomitrella patens) ecotypes to explore spermat

228 sible for protein import, we made transgenic moss (Physcomitrella patens) harboring the Km-altering m

229 Two moss (Physcomitrella patens) PPR proteins containing DYW

230 icot Arabidopsis (Arabidopsis thaliana), and moss (Physcomitrella patens) were examined through grazi

231 ssion of full-length recombinant factor H in moss (Physcomitrella patens).

232 In the moss, Physcomitrella patens, a 3D leafy gametophore orig

233 haromyces pombe), we generated a fluorescent moss (Physcomitrium [Physcomitrella] patens) ROP4 fusion

234 all plants examined in this study, including moss, possessed multiple structural features of tRNAs, w

235 In COS-7 cells expressing moss PpGLR1, ACC induces the highest cytosolic Ca(2+) el

236 t for mitochondrial and plastid proteomes in moss, present a novel multilevel approach to organelle b

237 Thus, we consider moss-produced recombinant human factor H a promising pha

238 ing events, and spectrally monitored the dry mosses' progression towards mortality.

239 significant number of novel AS events in the moss protonema.

240 tary components of mushrooms, pine nuts, and moss reflected forest gathering.

241 factor of 6; it is therefore enriched in the mosses, relative to Th, by a factor of 2.

242 y therefore be specific to immunity, and the moss relies on other pathways to respond to osmotic stre

243 hat a number of group II DUF231 members from moss, Selaginella, pine, spruce, rice and poplar were ma

244 ups (liverworts, mosses and hornworts), with moss sequences being most similar to those in vascular p

245 on from an intercalary region of determinate moss shoots.

246 aboveground plant C stocks, particularly in moss, shrubs and litter.

247 e and layer thickness were correlated on the moss site but not under shrub cover, where the canopy re

248 ted microbial community composition for both moss species and reduced N(2) -fixation rates for H. spl

249 We therefore examined whether liverwort and moss species have functional UVR8 proteins and whether t

250 We conclude that liverwort and moss species produce functional UVR8 proteins.

251 ascular plant species, crops, and a Sphagnum moss species, we detect a consistent reduction in the ph

252 SER/THR PROTEIN KINASE8 [STN8]) disclosed a moss-specific pattern of thylakoid protein phosphorylati

253 We propose that moss spermatozoids might be employed as an easily access

254 ffspring in a population of the aquatic peat moss Sphagnum macrophyllum.

255 d Picea mariana), and to a lesser extent one moss (Sphagnum fuscum), showed patterns of tissue N and

256 the spread of two novel tool-use variants, "moss-sponging" and "leaf-sponge re-use," in the Sonso ch

257 d strong evidence that diffusion patterns of moss-sponging, but not leaf-sponge re-use, were signific

258 ime a novice observed an informed individual moss-sponging.

259 a MS2 gene, which is highly expressed in the moss sporophyte, led to spores with highly defective wal

260 hat it negatively regulates branching in the moss sporophyte.

261 HLH and EPF components are also required for moss stomatal development and patterning.

262 it is required to activate transcription for moss stomatal development, as in A. thaliana(7).

263 We have demonstrated that mosses strongly influence C uptake and retention in Arct

264 ill interact with the relative abundances of mosses supporting different microbiomes and N(2) -fixati

265 Moss survival was assessed through growth experiments an

266 Gorlin-Chaudhry-Moss syndrome (GCMS) is a dysmorphic syndrome characteri

267 The desert moss Syntrichia caninervis, an extremophile, offers nove

268 Experiments on the desiccation-tolerant moss Syntrichia ruralis assessed the real-time dependenc

269 lear versus plastid genes are much higher in mosses than in seed plants, consistent with the emerging

270 Here we delete in a moss the P450 oxygenase that defines the entry point in

271 onse to these stimuli are present already in mosses, the oldest plant group with stomata, or were acq

272 In mosses these regulators are required for the deployment

273 uced ALTs, though were less influential than moss thickness.

274 In moss, this results in stochastic patterning of the filam

275 ixation rates in the soil, forest floor, and moss throughout three successional forests and along six

276 relation between polarization mechanisms in moss tip-growing cells and multicellular tissues of seed

277 Future studies will utilize FAAH mutants of moss to elucidate the role of anandamide in early land p

278 A transition from peat-forming Sphagnum moss to vascular plants has been observed in peatlands d

279 l as the uORF is conserved in GGP genes from mosses to angiosperms.

280 will alter the capacity of biocrust-forming mosses to modulate multiple ecosystem processes related

281 We conducted a moss transplant and leaf litter manipulation experiment

282 Mosses undergo such transitions: from two-dimensional ti

283 ture of the red alga Chondrus crispus (Irish Moss) using anatomical and optical approaches.

284 l in bitumen, is the only anomaly: in the AB mosses, V exceeds that of ancient peat by a factor of 6;

285 een in the fossil record and in rare natural moss variants.

286 ider biome, landscape position, and vascular/moss vegetation types when modeling CH4 production in pe

287 ctivities co-occurred in the water-submerged moss vegetation.

288 posit, but had contrasting vegetation cover (moss vs shrub).

289 Sphagnum moss was collected from 21 ombrotrophic (rain-fed) peat

290 Sphagnum moss was collected from ombrotrophic (rain-fed) peat bog

291 sands in northern Alberta, Canada, Sphagnum moss was obtained from 25 bogs near industrial operation

292 compositions of CO(2) and H(2)O in terms of moss water status and integrated isotope signals in cell

293 ng repair processes), at least some of these mosses were able to return to a metabolically active sta

294 Plant functional types such as shrubs and mosses were affected to a greater degree than other func

295 living vascular plants (e.g. litter, lichen, mosses) were associated negatively with climate change v

296 tary plasticity and consuming high levels of moss, which is exceptionally high in fibre and low in pr

297 pturing stress in precipitation-stressed dry mosses, while the SR and NPCI were highly effective.

298 Within their data set, we identified a moss with multiple LEAFY orthologs, which contests their

299 Higher deposition occurs in liverworts and mosses with specialized water-conducting cells.

300 l locations of southern Germany (DE), the AB mosses yielded lower concentrations of Ag, Cd, Ni, Pb, S