ライフサイエンスコーパス: subterranean

1 The effect of subterranean activity of ants on soil is well-studied, y

2 l, and physiological changes associated with subterranean adaptation within a comparative phylogeneti

3 ative, 4 subterranean and Pd-positive, and 1 subterranean and Pd-negative) during winter 2020-21 and

4 d-positive, 4 aboveground and Pd-negative, 4 subterranean and Pd-positive, and 1 subterranean and Pd-

5 effects of hibernaculum type (aboveground or subterranean) and Pd status (positive or negative) on wi

6 terns generated by ants, termites, and other subterranean animals are globally widespread, locally im

7 aves lacking primary productivity can expose subterranean animals to hypoxia.

8 Our results suggest that subterranean ant nest architecture is shaped by a combin

9 o form migratory slugs that translocate from subterranean areas to exposed sites, where they culminat

10 In the absence of visual signals, subterranean arthropods rely on olfactory and tactile cu

11 re CNE units and highlight the contrast that subterranean-associated coding region regression is high

12 Overall, our results indicate that subterranean atmospheres may be acting as sinks for atmo

13 issue, but its impact on the often-enigmatic subterranean biodiversity and its conservation remains p

14 ported by photosynthesis, including the vast subterranean biosphere and biospheres beneath ice sheets

15 logical and hydrological processes shape the subterranean biosphere.

16 Subterranean blind mole rats (Spalacidae) are considered

17 Zokors live at high elevation in subterranean burrows and experience hypobaric hypoxia, i

18 rats are eusocial rodents that live in large subterranean colonies in which one queen breeds with one

19 Naked mole-rats live in large, subterranean colonies where breeding is restricted to a

20 , and the prediction that, in the absence of subterranean connections, extreme genetic divergence bet

21 Parasitic members of this family form subterranean connections, or haustoria, on neighboring h

22 We tested the subterranean consequences of sea-level rise for cutoff w

23 Plants germinating under subterranean darkness assume skotomorphogenesis, a devel

24 critical initial emergence of seedlings from subterranean darkness into sunlight.

25 om buried seed grow vigorously upward in the subterranean darkness toward the soil surface.

26 s, including the StW 573 skeleton, come from subterranean deposits [T.

27 of the most significant constituents in the subterranean drilling processes to meet an increasing gl

28 The subterranean-dwelling naked mole-rat (NM-R; Heterocephal

29 n patterns worldwide have been attributed to subterranean ecosystem engineers such as termites, ants,

30 ground herbivore larval D. speciosa, and the subterranean ento-mopathogenic nematode natural enemy He

31 ole-rats are presumably adaptations to their subterranean environment and that they are the only know

32 yaluronic acid may benefit the adaptation to subterranean environment by increasing skin elasticity a

33 nes that changed at accelerated rates in the subterranean environment due to relaxed constraint and a

34 id Shallow Substratum (MSS), an understudied subterranean environment.

35 Lineages that have invaded subterranean environments have repeatedly evolved remark

36 xygen, commonly present at high-altitude and subterranean environments.

37 tionary adaptations occurring in response to subterranean environments.

38 Karst subterranean estuaries (KSEs) occur globally on carbonat

39 Subterranean estuaries (STEs) are critical ecosystems at

40 Subterranean estuaries (STEs) are of major importance fo

41 Subterranean estuaries (STEs), the zones in which seawat

42 Subterranean estuaries (STEs), where groundwater and sea

43 Subterranean estuaries extend inland into density-strati

44 carbon cycle and ecosystem function of karst subterranean estuaries.

45 t that the longer residence times within the subterranean estuary during the winter, which would resu

46 es of fresh-to-brackish groundwater from the subterranean estuary to reef ecosystems.

47 n coastal aquifers, groundwater transits the subterranean estuary, a region of sharp gradients in red

48 cled nutrients from the coastal ocean to the subterranean estuary.

49 reduction in nitrogen attenuation within the subterranean estuary.

50 two sensory systems repeated across multiple subterranean Eurycea lineages: the degeneration of the e

51 naked mole-rat (Heterocephalus glaber) is a subterranean eusocial rodent with a markedly long lifesp

52 ergone adaptive changes corresponding to the subterranean evolution of the blind mole rat.

53 miedaphic arthropods to selective aspects of subterranean existence are examined in light of overlapp

54 ve numerous anatomical specializations for a subterranean existence, including rows of sensory hairs

55 We evaluate the spatiotemporal patterns of subterranean fauna in MSS of iron duricrust (canga) in t

56 ifferences in the spatiotemporal patterns of subterranean fauna.

57 on, taxonomy and conservation of the cryptic subterranean fauna.

58 in local gravity enables the observation of subterranean features.

59 insect dispersal when growing on aggregated subterranean fecal pellets of a plant-feeding insect.

60 , shales) becomes an important new branch of subterranean fluid mechanics.

61 gh the injection of water and proppants into subterranean formations.

62 s is threatening its evolutionarily distinct subterranean freshwater fauna, some taxa of which repres

63 Amphicarpic plants produce aerial and subterranean fruits on an individual plant, and these he

64 pread of H(2) through leaky pipes, wells, or subterranean gas migrations on groundwater resources and

65 It is similar to extant subterranean golden moles in having reduced digit segmen

66 ical rainforest across four vertical strata: subterranean, ground, understory and canopy.

67 processes such as groundwater extraction and subterranean groundwater discharge to oceans could resul

68 agnitude of the DIC flux to the oceans by US subterranean groundwater discharge.

69 an investigation is complicated by both its subterranean habit and the persistence of genotypes over

70 owledge for understanding adaptations to the subterranean habitat.

71 tudies on organisms adapted to nutrient poor subterranean habitats are few and far between.

72 Many species adapted to aphotic subterranean habitats have lost all body pigmentation.

73 yidae) are restricted to specialised coastal subterranean habitats or nearby freshwaters and have a h

74 ions using 14 species of waterlice living in subterranean habitats with contrasted levels of radioact

75 s an apomorphy associated with adaptation to subterranean habitats, but in isopods it appeared to be

76 symplesiomorphy unrelated to colonization of subterranean habitats.

77 mes, specifically, the gain of D1 claws with subterranean habits and the loss of D1 ungues with oral-

78 ased approach when applied to organisms with subterranean habits.

79 These subterranean ice deposits show widespread evidence of ac

80 ral, genetic, and geologic data from a young subterranean insect lineage in lava tube caves on Hawai'

81 enus Eurycea), with independent invasions of subterranean karstic environments, offers an opportunity

82 Its subterranean larval stages are hard to reach with pestic

83 Conversely, species with subterranean larval stages have relatively constant dura

84 roorganisms that live in soil using modified subterranean leaf structures (rhizophylls).

85 th recent observations of nematodes over its subterranean leaves, prompted the suggestion that the ge

86 ax mexicanus populations are well adapted to subterranean life and many populations appear to have ev

87 ctivity was modified during the evolution of subterranean life and shows that tissue-specific promote

88 sis of loss of eye function-an adaptation to subterranean life-reveals a structured order of loss of

89 ndicates that they had most likely adopted a subterranean lifestyle by the mid-Cretaceous, occupying

90 ole-rat's (Heterocephalus glaber) social and subterranean lifestyle generates a hypoxic niche.

91 ecular-mass hyaluronic acid has evolved with subterranean lifestyle.

92 assic docodontan shows specializations for a subterranean lifestyle.

93 e, perhaps tailoring hearing to eusocial and subterranean lifestyles.

94 The increase in anterior neuromast organs in subterranean lineages was positively correlated with the

95 eting signs of unrest in terms of the causal subterranean magmatic processes.

96 Using a benchmarking case of convergent subterranean mammal adaptation, phyloConverge identifies

97 hat contributes to cancer resistance of this subterranean mammal extremely adapted to life undergroun

98 we examined the SC of the star-nosed mole, a subterranean mammal that, instead of using vision, explo

99 These subterranean mammalian species accumulate abundant high-

100 hyaluronic acid is found in a wide range of subterranean mammalian species, but not in phylogenetica

101 studied convergence in evolutionary rate in subterranean mammals in order to associate phenotypic ev

102 for future neuroanatomical investigations of subterranean mammals.

103 tern produced by inactivated vision genes in subterranean mammals.

104 ng to around AD 500-900 that were found in a subterranean mass burial near the Sacred Cenote (sinkhol

105 se findings reveal a heretofore unrecognized subterranean methane sink and contribute to our understa

106 The blind subterranean mole rat is a model for hypoxia tolerance w

107 The blind subterranean mole rat of the Spalax ehrenbergi superspec

108 and analyzed expression of Flk1 in the blind subterranean mole rat Spalax ehrenbergi.

109 In its natural habitat, the strictly subterranean naked mole-rat (Heterocephalus glaber) has

110 The strictly subterranean naked mole-rat (Heterocephalus glaber) has

111 domestication analyses owing mostly to their subterranean nature.

112 protrude from the ground meters above their subterranean nests.

113 mammals, suggesting that species occupying a subterranean niche do not exhibit baseline metabolic cos

114 while "disordered" domains were conserved in subterranean organisms, and confirmed for proteins in Di

115 The surface and subterranean populations were genetically distinct, with

116 c evidence we suggest that these specialized subterranean predators are the sole surviving representa

117 uatic island biogeography, especially in the subterranean realm.

118 o (Ctenomys sociabilis), a social species of subterranean rodent that is endemic to southwestern Arge

119 The naked mole-rat is a subterranean rodent, approximately the size of a mouse,

120 land mole rats (Fukomys damarensis), another subterranean rodent.

121 ear innervation specifically between the two subterranean rodents and more broadly among rodents prov

122 Blind mole rats Spalax (BMR) are small subterranean rodents common in the Middle East.

123 African mole-rats are subterranean rodents inhabiting underground burrows.

124 For subterranean rodents such as the naked mole-rat, propose

125 African naked mole-rats are subterranean rodents that have a robust orienting respon

126 e explored a system involving two species of subterranean rodents that present morphological, karyoty

127 African mole-rats are subterranean rodents that spend their whole life in unde

128 Naked mole-rats are highly vocal, eusocial, subterranean rodents with, counterintuitively, poor hear

129 Zokors, an Asiatic group of subterranean rodents, originated in lowlands and coloniz

130 om nymph to adult, during which a shift from subterranean root-feeding to feeding on aboveground part

131 n the volatile organic compounds used by the subterranean root-knot nematode (RKN) Meloidogyne incogn

132 tions in the development of optic systems in subterranean salamander lineages.

133 Aerial seed yield was affected more than subterranean seed yield by shading intensity.

134 Aerial and subterranean seed yield, seed mass and number for both A

135 life cycle from aerial seeds (ASP) and from subterranean seeds (SSP).

136 ch is a key evolutionary adaptation vital to subterranean social insects such as termites and ants.

137 tude lakes are best explained as supplied by subterranean sources (within the last 10,000 years), whi

138 nana) relative to the maintained labeling in subterranean species (Eurycea rathbuni).

139 Subterranean species dependent on touch have particularl

140 ast to fossorial and above-ground organisms, subterranean species have adapted to the extreme stresse

141 Consequently, many subterranean species have evolved low basal metabolism a

142 pt significantly less optimal codon usage in subterranean species than in fossorial and above-ground

143 imposes unique demands on life that have led subterranean species to evolve specialized traits, many

144 s for producing the specialized corticies of subterranean species.

145 e twice as dark as assemblages in ground and subterranean strata.

146 nd-penetrating radar to discern long-hidden, subterranean structures.

147 g those of stress-response genes, among nine subterranean, ten fossorial, and 13 aboveground species.

148 We therefore propose that subterranean termite (Rhinotermitidae) colony growth is

149 y looks at dietary nitrogen acquisition in a subterranean termite (Rhinotermitidae, Coptotermes).

150 the nest and ingest decaying wood; therefore subterranean termite colonies should have mechanisms to

151 Here we show that a subterranean termite Coptotermes formosanus Shiraki comb

152 omic resources become available, and as more subterranean termite researchers incorporate molecular t

153 olony fusion benefits social immunity in the subterranean termite Reticulitermes flavipes.

154 as model to simulate tunnels of the Formosan subterranean termite, Coptotermes formosanus Shiraki.

155 We found no evidence that subterranean termites (Reticulitermes) were influenced b

156 niques have made contributions to studies on subterranean termites at all levels of biological organi

157 The majority of subterranean termites continuously forage for new wood r

158 Subterranean termites excavate tunnels in a search patte

159 lationship between diazotrophic bacteria and subterranean termites may primarily be trophic rather th

160 Recent results on the behavioral ecology of subterranean termites reveal a picture different from lo

161 ts, Monomorium pharaonis (Linnaeus), eastern subterranean termites, Reticulitermes flavipes (Kollar),

162 In subterranean termites, some workers forage for and explo

163 , community ecology, and invasion biology of subterranean termites.

164 and insects (Class Insecta); three habitats: subterranean, terrestrial and airborne; and three integr

165 y ants vary in microhabitat use from largely subterranean to largely above-ground active species and

166 within anthropogenic 'caves'; the Iron-Age, subterranean tombs of central Italy.

167 ire ant Solenopsis invicta, which constructs subterranean tunnel networks (nests).

168 remodeled shells of social hermit crabs, the subterranean tunnel systems of naked mole rats, the intr

169 agma build-up before volcanic eruptions, and subterranean tunnels.

170 ty associated with fully pelagic, cursorial, subterranean, volant, and other lifestyles.

171 this recently described snakehead fish from subterranean waters of Kerala in South India.

172 dwelling amphibian Proteus anguinus inhabits subterranean waters of the north-western Balkan Peninsul

173 i.e., burrows, streams, standing waters, and subterranean waters).

174 The subterranean world hosts up to one-fifth of all biomass,