ライフサイエンスコーパス: bryophyte

1 ermination (UV systems, as in some algae and bryophytes).

2 ens, in the sister group of vascular plants (Bryophytes).

3 a vascular plant reported to transpose in a bryophyte.

4 served among vascular plants, but not in the bryophytes.

5 implications for mating system evolution in bryophytes.

6 rasses, dicotyledons, ferns, Selaginella and bryophytes.

7 ation of maternal chloroplast inheritance in bryophytes.

8 osperms, limited information is available in bryophytes.

9 ependently of WUSCHEL-like (WOX) proteins in bryophytes.

10 plant weeds but is ineffective against many bryophytes.

11 ens (Physcomitrella), in the moss lineage of bryophytes.

12 oteins originated prior to the divergence of bryophytes.

13 of genes than TEs were repressed by PRC2 in bryophytes.

14 f liverworts and mosses, within monophyletic bryophytes.

15 a), coinciding with the land colonization by bryophytes.

16 lectron micrographs of the anatomy of extant bryophytes.

17 tolerant food-conducting cells (leptoids) of bryophytes.

18 studies that include both tracheophytes and bryophytes.

19 dent-may account for glyphosate tolerance in bryophytes.

20 ast to angiosperms, unisexuality prevails in bryophytes.

21 ogenetically independent sample of Amazonian bryophytes.

22 t bioactive gibberellins might be present in bryophytes, although they have yet to be detected experi

23 and the rapid establishment of a productive bryophyte and lichen layer on the surface.

24 the formation of nonvascular epiphyte (i.e. bryophyte and lichen) mats.

25 We hypothesized that bryophyte and lycophyte photosynthesis is largely limite

26 photosynthesis and anatomical parameters in bryophyte and lycophyte species in Antarctica, Australia

27 d back to a time after the divergence of the bryophyte and spermatophyte lineages, but before the spl

28 Thus, bryophytes and algae likely lack the glycosyltransferase

29 I focus on the relationship between bryophytes and angiosperms as a case study, but the them

30 nserved defense mechanisms present in extant bryophytes and angiosperms, as well as moss-specific def

31 hornworts to establish synapomorphies across bryophytes and approach a definition of the ancestral ch

32 basis of key functional variation within the bryophytes and between the bryophytes and other land pla

33 , PGDD contains data for 26 plants including bryophytes and chlorophyta, as well as angiosperms with

34 ion, MYCs are functionally conserved between bryophytes and eudicots.

35 ametophyte development by the protonemata of bryophytes and ferns.

36 tion during germination is conserved between bryophytes and flowering plants and analyse the underlyi

37 scovered a phylogenetic clade shared between bryophytes and higher land plants of monocot grass and d

38 Both terrestrial insects and the bryophytes and lichens group increased in average occupa

39 ions of over 5,000 species of invertebrates, bryophytes and lichens, measured as changes in occupancy

40 Photosynthesis in bryophytes and lycophytes has received less attention th

41 ures of JAZ proteins, which are conserved in bryophytes and lycophytes, enable perception of dn-OPDA

42 evidenced by the conserved gene order among bryophytes and lycophytes, whereas ferns, gymnosperms, a

43 (WOX) gene family, which is absent in extant bryophytes and lycophytes.

44 uphyllophytes but also occur in non-vascular bryophytes and non-seed lycophytes.

45 iation within the bryophytes and between the bryophytes and other land plants.

46 were in some cases as productive as lichens, bryophytes and plants that resided nearby.

47 s to a growing body of genomic resources for bryophytes and provides an important perspective on the

48 n both animals and early land plants such as bryophytes and pteridophytes.

49 previously observed in other DT green algae, bryophytes and resurrection plants, other traits being d

50 are transitional evolutionary grades between bryophytes and seed plants, and has important implicatio

51 about the acetylation patterns of mannans in bryophytes and seedless vascular plants, and the evoluti

52 compose the following two sister groups: the bryophytes and the vascular plants.

53 r of land plants, prior to the divergence of bryophytes and tracheophytes and, secondly, there has be

54 Bryophytes and tracheophytes are descendants of early la

55 hese involved the evolution of embryophytes (bryophytes and tracheophytes) from a charophycean ancest

56 d two divergent evolutionary trajectories in bryophytes and tracheophytes, eventually influencing dis

57 mpared with new and published SEMs of extant bryophytes and tracheophytes, respectively.

58 In embryophytes, including both bryophytes and tracheophytes, the haploid gametophytic g

59 es and likely predates the divergence of the bryophytes and tracheophytes.

60 ish the permanent cryptospore-producers from bryophytes and tracheophytes.

61 ompass a pool of diversity from which modern bryophytes and vascular plants emerged, but were competi

62 An initial split between bryophytes and vascular plants implies that the bryophyt

63 biosynthesis pathway after the divergence of bryophytes and vascular plants.

64 Both types of Glbs occur in green algae, bryophytes and vascular plants.

65 n several mono- and dicotyledonous plants, a bryophyte, and three algae, revealing a correlation of G

66 The non-seed plants (e.g., charophyte algae, bryophytes, and ferns) have multiple human uses, but the

67 la moellendorffii, after the divergence from bryophytes, and later emerged in gymnosperms and angiosp

68 h arrest that were already present in ferns, bryophytes, and possibly in algae.

69 an O-acetyltransferases probably occurred in bryophytes, and the biochemical functions of these O-ace

70 However, little is known about stomata in bryophytes, and their evolutionary origins and ancestral

71 lishing a symbiosis with plants, such as the bryophyte Anthoceros punctatus.

72 sporophyte retention on the gametophyte is a bryophyte apomorphy.

73 siderable support to the conclusion that the bryophytes are a monophyletic group.

74 nalyses reveal that extant tracheophytes and bryophytes are both highly derived from a more complex a

75 ributional patterns suggesting that tropical bryophytes are highly vagile, our analyses reveal spatia

76 re present, an effect not observed when only bryophytes are present.

77 targeting mammals, fish, amphibians, birds, bryophytes, arthropods, copepods, plants and several mic

78 Our analyses resolved bryophytes as a monophyletic group and showed that the n

79 sperms, gymnosperms, pteridophytes, and some bryophytes as a strategy for enhancing phosphate acquisi

80 related to the bryophytes, but they are not bryophytes as defined by extant representatives.

81 es have identified liverworts, hornworts and bryophytes as each being the first lineage of land plant

82 The exhumed bryophyte assemblages have exceptional structural integr

83 COS (A(S) ) uptake rates from two astomatous bryophytes at different relative water contents (RWCs),

84 d plants are also present in charophytes and bryophytes, at least in nascent forms.

85 Vascular plants and bryophytes (basally diverging land plants) develop later

86 predicted protein-protein interactome for a bryophyte based on the interolog method contains 67,740

87 ring water limiting conditions thus offering bryophyte-based strategies for crop improvement for drou

88 Additionally, the proportion of bryophyte biomass increases, whereas that of shrub bioma

89 Regeneration of subglacial bryophytes broadens the concept of Ice Age refugia, trad

90 The desiccation tolerant bryophyte Bryum argenteum is an important component of d

91 he protein is conserved in higher plants and bryophytes but absent in algae and cyanobacteria.

92 Clade-D ARFs are present in lycophytes and bryophytes but absent in other plant lineages.

93 -like transporters that originated after the bryophytes but before or within the lycophytes.

94 have been lost in all but a few lineages of bryophytes but, strikingly, within the liverworts a deri

95 estral land plants that has been retained in bryophytes, but rewired in flowering plants for male ger

96 arose by convergence in vascular plants and bryophytes, but the trajectory of branching form diversi

97 Others are more closely related to the bryophytes, but they are not bryophytes as defined by ex

98 We estimated bryophyte C:N:P ratios and their biogeochemical niches,

99 onal genetic studies between angiosperms and bryophytes can define those genetic changes that were re

100 ed with the Ordovician-Silurian evolution of bryophytes, challenging a paradigm that deep-rooted plan

101 ures (e.g. pegged rhizoids) could help track bryophyte clades or water conductance evolution in the f

102 Understanding how changing climate affects bryophyte contributions to global cycles in different ec

103 Biotic COS production in bryophytes could result from symbiotic fungal and bacter

104 decade, while species evenness of herbs and bryophytes declines by 14 and 8%, respectively.

105 Bryophytes develop haploid spores with an analogous func

106 diverging from other land fungi paralleling bryophyte divergence, are related to arbuscular mycorrhi

107 totrophic and heterotrophic respiration in a bryophyte-dominated peatland in Abisko, Sweden.

108 Here we show that extant bryophytes exhibit submergence-induced developmental pla

109 ast, UV sex chromosomes, like those found in bryophytes, experience symmetrical population genetic co

110 eptophyta includes the Charophyceae plus the bryophytes, ferns, and all other multicellular land plan

111 trial plant species spanning diverse clades (bryophytes, ferns, gymnosperms, and flowering plants), w

112 Dispersal limitation for tropical bryophytes flies in the face of traditional assumptions

113 unique successful regeneration of subglacial bryophytes following 400 y of ice entombment.

114 For bryophytes, fossils have been excluded from previous ass

115 The oldest unambiguous bryophyte gametophytes (thalli) are from the upper Middl

116 By contrast, two divisions of bryophyte gametophytes and moss sporophytes are reported

117 d branching in flowering plants does not fit bryophyte gametophytes.

118 he land plants and the mechanisms regulating bryophyte gametophytic shoot development are largely unk

119 he Huperzia chloroplast genome possesses the bryophyte gene order for a previously characterized 30 k

120 fically, genome collinearity between the two bryophyte genomes and vascular plants is limited, sugges

121 These newly sequenced bryophyte genomes offer a valuable resource for explorin

122 analysis, incorporating 123 newly sequenced bryophyte genomes, reveals that bryophytes possess a sub

123 Advances in bryophyte genomics and the phylogenetic recovery of horn

124 e of many peatland ecosystems is Sphagnum, a bryophyte genus of c.

125 used on identifying herbarium specimens of a bryophyte group, peat mosses in Sphagnum subgenus Sphagn

126 es diverged substantially in the nonvascular bryophyte groups (liverworts, mosses and hornworts), wit

127 show no light-activated change in turgor in bryophyte guard cells, with pressures not significantly

128 On average, lycophytes and, specially, bryophytes had the lowest photosynthetic rates and nonst

129 In bryophytes, haploid gametophytes grow via clonal propaga

130 Bryophytes harbour microbiomes, including diverse commun

131 wever, because of their small physical size, bryophytes have been largely ignored in research on wate

132 Lowland tropical bryophytes have been perceived as excellent dispersers.

133 reviously envisioned and that the stomata of bryophytes have undergone reductive evolution, including

134 entified in green and brown algae as well as bryophytes, have also evolved in red algae, contributing

135 ly closest modern relatives of early plants, bryophytes, have been largely neglected.

136 portunity for postfertilization selection in bryophytes having short fertilization distances and spat

137 nge, resulting in shifts in the magnitude of bryophyte impacts on global ecosystem functions.

138 ol due to its key phylogenetic position as a bryophyte in the post-genomic era.

139 Here, we resolve the position of bryophytes in the land plant tree and investigate the ev

140 Bryophytes, including the lineages of mosses, liverworts

141 Species richness of shrubs and bryophytes increases by 8 and 11% per decade, while spec

142 Here, we review the literature on how bryophytes influence global biogeochemical cycles, and w

143 e to changing climate, the size of different bryophyte-influenced biomes will change, resulting in sh

144 d that the post-glacial assembly of European bryophytes involves a complex history from multiple sour

145 jectory of branching form diversification in bryophytes is unclear.

146 cryptogamic covers, such as cyanolichens and bryophytes, is a primary source of fixed nitrogen in pri

147 e conserved stomatal morphology, the sampled bryophytes lack dynamic control over guard cell turgor t

148 proxylic beetles, vascular plants, epiphytic bryophytes, lichens, and wood-inhabiting fungi, as well

149 Nonvascular photoautotrophs (NVP), including bryophytes, lichens, terrestrial algae, and cyanobacteri

150 We conclude that the reason why bryophytes lie at the lower end of the leaf economics sp

151 ophytes and vascular plants implies that the bryophyte life cycle (with a dominant gametophyte nurtur

152 micro-refugia, which was unexpected based on bryophyte life-history traits, and of southern refugia,

153 ascular plant lineage after diverging from a bryophyte-like ancestor nearly 500 million years ago.

154 s the hypothesis that early land plants were bryophyte-like and possessed a dominant gametophyte and

155 Specifically, bryophytes limited colonization by new species into loca

156 Mosses are the most species-rich bryophyte lineage and two sub-groups are circumscribed b

157 esent evidence for neochrome in hornworts (a bryophyte lineage) and demonstrate that ferns acquired n

158 on factor genes before the divergence of the bryophyte lineage.

159 eds were acquired after the evolution of the bryophyte lineage.

160 Bryophyte lineages were the earliest diverging embryophy

161 ll secreted peptides in the genomes of three bryophyte lineages-mosses, liverworts and hornworts-that

162 is useful for inferring relationships among bryophyte lineages.

163 imate in representative species of the three bryophyte lineages.

164 ntial existence of CHI proteins in the basal bryophyte liverwort species and the lycophyte Selaginell

165 m angiosperms and non-angiosperms (including bryophytes, lycophytes, ferns and gymnosperms) are able

166 Our phylogenetic analyses of miRNAs in bryophytes, lycophytes, ferns, and angiosperms refine th

167 s in 35 land plant species including mosses, bryophytes, lycophytes, gymnosperms, and angiosperms.

168 from all lineages of land plants, including bryophytes, lycopods, ferns and seed plants.

169 s (PUCs; e.g., epilithon, filamentous algae, bryophytes, macrophytes) in human-impacted aquatic ecosy

170 untries, the proportions of vascular plants, bryophytes, mammals, reptiles, dragonflies, and grasshop

171 s received almost no research attention, the bryophytes manifest a wide range of developmental respon

172 dless plant lineages, ferns, lycophytes, and bryophytes, many of these candidate genes are mainly exp

173 ivalent role in symbiosis maintenance in the bryophyte Marchantia paleacea and is part of a broad AM

174 a collection of 133 accessions of the model bryophyte Marchantia polymorpha and studied its intraspe

175 We used the bryophyte Marchantia polymorpha, which diverged from vas

176 inct modules with different functions in the bryophyte Marchantia polymorpha.

177 Silica extracted from bryophyte material through wet-ashing was described, foc

178 resent critical tipping points for survival, bryophytes may also buffer many ecosystems from change d

179 Alternatively, MurA in bryophytes may bind glyphosate, thereby leaving more unb

180 Polyandry in bryophytes may occur among multiple sporophytes of a fem

181 results suggest that ecosystems dominated by bryophytes might be strong atmospheric sinks of COS at n

182 Physcomitrella patens is a bryophyte model plant that is often used to study plant

183 Our analyses recover bryophyte monophyly and demonstrate that the guard cell

184 entative of the earliest plants on land, the Bryophyte moss Physcomitrella patens.

185 resolve tracheophytes (vascular plants) and bryophytes (non-vascular plants) as monophyletic sister

186 Of the three lineages of bryophytes, only the mosses and the liverworts are syste

187 We found that bryophyte or lycophyte BRX homologs can only partially s

188 ubstantial pretracheophyte fossil record for bryophytes (otherwise predicted by molecular systematics

189 As a member of the bryophytes, P. patens provides a unique opportunity to s

190 greenish-brown) and microhabitats (lichen or bryophyte patches), compared to non-occupied trunks.

191 regulation of spore germination in the model bryophyte Physcomitrella patens (Aphanoregma patens).

192 The model bryophyte Physcomitrella patens exhibits high frequencie

193 The bryophyte Physcomitrella patens has a single TPS gene, c

194 toolbox genes, and manipulation in the model bryophyte Physcomitrella patens has shown that the bHLH

195 g most phases in the life cycle of the model bryophyte Physcomitrella patens, including detailed spor

196 d development in the gametophytes (n) of the bryophyte Physcomitrella patens.

197 development in Arabidopsis thaliana) in the bryophyte Physcomitrella patens.

198 we examined the role of RAD51B in the model bryophyte Physcomitrella patens.

199 -member phytochrome gene family in the model bryophyte Physcomitrium (Physcomitrella) patens.

200 nisms underlying the defense response of the bryophyte Physcomitrium patens (previously Physcomitrell

201 are transcriptional activators in the model bryophyte Physcomitrium patens and have a major role in

202 , we investigated the roles TPL plays in the bryophyte Physcomitrium patens, which diverged from angi

203 We also assessed the diagnostic value of bryophyte phytoliths.

204 growth is essential for land colonization by bryophytes, plant sexual reproduction and water and nutr

205 ly sequenced bryophyte genomes, reveals that bryophytes possess a substantially greater diversity of

206 Bryophytes provide a unique system to explore this relat

207 on-year history of plants on land belongs to bryophytes, pteridophytes and gymnosperms, which eventua

208 has important implications for understanding bryophyte reproduction, suggesting the presence of a sig

209 s terrestrial ecosystems has highlighted how bryophytes retain and control water, fix substantial amo

210 The evolution of bryophytes' rich and diverse genetic toolkit, which incl

211 etics extending beyond flowering plants into bryophytes, scientists have started to unravel the genet

212 are an abundant cell wall polysaccharide in bryophytes, seedless vascular plants and gymnosperms.

213 The vegetative gametophyte meristems of bryophytes share some characteristics with the shoot api

214 We found that bryophytes shared common predicted small secreted peptid

215 Overall, this genome and those of other 2 bryophytes show that mitochondrial genomes in early land

216 en hypothesized that predecessors of today's bryophytes significantly increased global chemical weath

217 Bryophyte sister lineages to the vascular plants lack su

218 Na, Mg, Ca, S, Fe) of 35 widely distributed bryophyte species inhabiting springs.

219 size that, as in gymnosperms, the low extant bryophyte species richness also results from massive ext

220 e spatial predictions of forest ground-floor bryophyte species richness in Limburg (Belgium), based o

221 do not fully account for current patterns of bryophyte species richness, and we hypothesize that, as

222 ression in natural populations of a dioicous bryophyte species, Sphagnum lescurii, using microsatelli

223 lete guard cell turgor loss had no effect on bryophyte stomatal aperture but resulted in partial or c

224 matal anatomy with the earliest land plants, bryophyte stomatal behavior may provide insights into th

225 wer tolerance of M. inflexa relative to most bryophytes studied to date.

226 We also show that a major component of the bryophyte submergence response is controlled by the phyt

227 terized by a burst of gene innovation, while bryophytes subsequently experienced an equally dramatic

228 iated with biomass across shrubs, herbs, and bryophytes, suggesting that changes in diversity alter u

229 ubstantial silica accumulation in tissues of bryophytes suggests that silica (phytolith) deposition e

230 Data from modern bryophytes suggests this plentiful early plant material

231 ark- vs. light-acclimated guard cells across bryophyte taxa with stomata, where their role in gas-exc

232 We show in bryophytes that abscisic acid (ABA) pretreatment of moss

233 Here we report a macro2 domain gene in bryophytes that is likely derived from Mucoromycota, a g

234 hornworts, altogether forming the lineage of bryophytes that shared a common ancestor with land plant

235 reen alga group closest to the land plants), bryophytes (the most basal land plants), pteridophytes (

236 ding demonstrates the totipotent capacity of bryophytes, the ability of a cell to dedifferentiate int

237 plants and the two of the three lineages of bryophytes, the mosses and liverworts, is steadily accum

238 n biodiversity patterns, but their impact on bryophytes, the second most diverse group of land plants

239 rial plants, possibly early relatives of the bryophytes, this interpretation remains controversial as

240 spite their small size and simple structure, bryophytes thrive in a wide variety of habitats, includi

241 yscomitrella patens UVR8 in experiments with bryophyte tissue and expression of green fluorescent pro

242 In polar ecosystems, regrowth of bryophyte tissue buried by ice for 400 y significantly e

243 ametophyte generation-dominant life cycle in bryophytes to a diploid sporophyte generation-dominant l

244 ying divergence of land plants spanning from bryophytes to angiosperms.

245 orescences, floral organs, and nodules) from bryophytes to higher flowering plants.

246 uncertainty concerning the relationships of bryophytes to one another and to the tracheophytes, as w

247 However, as the thresholds of resistance of bryophytes to temperature and precipitation regime chang

248 angiosperm (one newly sequenced), and eight bryophytes using bioinformatics, conventional cytogeneti

249 on purpureus to test for degeneration in the bryophyte UV sex chromosomes.

250 Hence, the ancestral genome of bryophytes was likely a patchwork of units of euchromati

251 green algae and most basal land plants, the bryophytes, we evaluated the presence of this signaling

252 dicotyledonous angiosperms, gymnosperms, and bryophytes, were produced in insect cells, and each CslA

253 eas the cover of those colonists, along with bryophytes, were the primary drivers of local extinction

254 AT4/6/8 arose early in land-plant evolution (bryophytes), whereas the phosphatase-minus GPAT1 to -3 a

255 en in the liverwort Marchantia polymorpha, a bryophyte, which produces gametophyte axes with nonphoto

256 lts emphasize the unrecognized resilience of bryophytes, which are commonly overlooked vis-a-vis thei

257 Unraveling the macroevolutionary history of bryophytes, which arose soon after the origin of land pl

258 yletic lineages, the vascular plants and the bryophytes, which diverged from their most recent common

259 on of this major metabolic pathway in extant bryophytes, which represent the non-vascular stage of em

260 o deeply divergent groups, tracheophytes and bryophytes, which shared a common ancestor some 500 mill

261 uctive stomatal evolution, especially in the bryophytes (with complete loss in the liverworts).