ライフサイエンスコーパス: monophyly

1 econciling molecular support for the group's monophyly.

2 under evolutionary models about features of monophyly.

3 mertea but are unable to reject deuterostome monophyly.

4 al tests rejected both Archonta and microbat monophyly.

5 indicating a lack of mitochondrial sequence monophyly among species.

6 ugh recent studies unambiguously support bat monophyly and consensus is rapidly emerging about evolut

7 nt classes further confirms siliceous sponge monophyly and demosponge-hexactinellid spicule homology,

8 This finding is consistent with Chromista monophyly and implicates secondary endosymbiosis as an i

9 me molecular studies also challenge microbat monophyly and instead support an alliance between megaba

10 We found strong phylogeographic monophyly and large genetic distances between N. n. nebu

11 ic analyses confirm hypotheses of lemuriform monophyly and provide robust resolution of the phylogene

12 simony analyses all contradict macroglossine monophyly and provide support for an African clade that

13 ve innovations that strongly support unikont monophyly and the primary bikont/unikont bifurcation.

14 lationships in the Acercaria, supporting its monophyly, and questioning the position of Psocodea as s

15 ence among isolates, nearly complete species monophyly, and widespread geographic distribution sugges

16 Aspects of monophyly are therefore central to fields that examine a

17 s as sister to all other animals, and sponge monophyly, are strongly supported under multiple analyse

18 + matK and rbcL + matK + trnH-psbA) using a monophyly-based method (GARLI).

19 This monophyly can be divided into four subfamilies, and each

20 Parametric bootstrapping tests reject monophyly for Arthropoda and Nemertea but are unable to

21 Coleoptera, and Diptera) but do not support monophyly for Deuterostomia, Arthropoda, or Nemertea.

22 The ATPase-based trees support monophyly for several clades (including Lophotrochozoa,

23 Monophyly for suborder Annulipalpia sensu stricto also i

24 u stricto also is widely acknowledged, as is monophyly for suborder Integripalpia sensu stricto.

25 Monophyly for Trichoptera seems well argued.

26 Monophyly for Yponomeutoidea was supported very strongly

27 This assumption of monophyly has been generally validated by independent da

28 hylogenetically and structurally distinctive monophyly in Archaeplastida.

29 se results and supports traditional microbat monophyly, inclusive of representative rhinolophoids fro

30 atic statistical analyses have shown whether monophyly is the rule across all HPV open reading frames

31 have been tacitly assumed, although microbat monophyly is uncorroborated by molecular data.

32 Resolution of the microbat paraphyly/monophyly issue is essential for reconstructing the temp

33 viruses, that are reported to share the same monophyly lineage as chloroviruses.

34 The respective monophylies of the two suborders have been tacitly assum

35 erful statistical evidence corroborating the monophyly of all known life.

36 es, the trees neither refute nor support the monophyly of Apusozoa.

37 ith the addition of these sequences indicate monophyly of Archaea, with modest bootstrap support.

38 ly as the cetacean sister group and supports monophyly of artiodactyls.

39 LSU and SSU data agree in supporting the monophyly of Bilateria, Cnidaria, Ctenophora, and Metazo

40 polyphyletic, however we fail to reject the monophyly of Cambarus with a topology test.

41 ced within the order Pleuronematida; (6) the monophyly of classes Phyllopharyngea, Karyorelictea, Arm

42 ut without true shells, and they support the monophyly of Conchifera.

43 The monophyly of Copepoda (including Platycopioida Fosshagen

44 investigated by estimating their support to monophyly of cultivars.

45 us with regard to nonmolecular characters as monophyly of Cyanocorax.

46 Together, these data support the monophyly of cyclostomes and suggest that the last commo

47 The topologies support the monophyly of Delphacinae and its basal split into three

48 ees in their strong support for the separate monophyly of domains as well as the early evolution of t

49 Our analyses support the monophyly of DPANN (Diapherotrites, Parvarchaeota, Aenig

50 The monophyly of each order is well established, but interre

51 The monophyly of Ecdysozoa, molting organisms, was not suppo

52 (elephants) and Sirenia (sea cows), and the monophyly of echolocating Chiroptera (bats).

53 s Avialae, with implications for, first, the monophyly of Enantiornithes and Sauriurae; second, the p

54 rived from these subfossils corroborates the monophyly of endemic Malagasy primates.

55 Analyses of 185 genes resulted in reciprocal monophyly of Enteropneusta and Pterobranchia, placed the

56 re well resolved with strong support for the monophyly of Evacanthinae and its four previously includ

57 There is strong support overall for monophyly of families previously recognized on morpholog

58 es A and B recapitulate the species-specific monophyly of FIV marked by high levels of genetic divers

59 bfamilies reveals high levels of support for monophyly of Hominidae, tribe Hominini and subtribe Homi

60 hyletic Lethrinidae did not resolve, but the monophyly of Lethrinus is well supported.

61 gene transfer, leading some to question the monophyly of life.

62 l the remaining Lygaeoidea, and supports the monophyly of Lygaeoidea.

63 wo cicadomorphan superfamilies supported the monophyly of Membracoidea, and indicated that treehopper

64 ese studies have concluded that the observed monophyly of metastatic subclones favored metastasis-to-

65 pods), and provide molecular support for the monophyly of molluscs, a group long recognized by morpho

66 sister to other euarthropods, and indicates monophyly of Myriapoda and Mandibulata.

67 of interfamilial relationships and supports monophyly of neotropical tapirs.

68 spider tree and all reject the long-accepted monophyly of Orbiculariae, by placing the cribellate orb

69 psbA tree shows significant support for the monophyly of peridinin- and fucoxanthin-containing dinof

70 Our analyses reject monophyly of plant R-proteins and NLRs and suggest that

71 support for clade L and weak support for the monophyly of Pleuronectiformes.

72 lies as evolutionary characters supports the monophyly of poxviruses, asfarviruses, iridoviruses, and

73 Monophyly of Pycnogonida, Euchelicerata, Myriapoda, Tetr

74 p between passerines and parrots and the non-monophyly of raptorial birds in the hawk and falcon fami

75 yze 60,000 novel red algal genes to test the monophyly of red + green (RG) algae and their extent of

76 dentified 30 trees that support the expected monophyly of red and green algae/plants (i.e. the Planta

77 GS: A new phylogenetic analysis supports the monophyly of saber-toothed cats (Machairodontinae) exclu

78 Our model robustly rejects monophyly of SAR11, classifying all but one strain as Rh

79 oversial ascaridomorph clades, including the monophyly of superfamilies and families, except for Asca

80 This result supports the monophyly of the "robust" australopiths and suggests tha

81 However, the monophyly of the Acantharea and the separate monophyly o

82 alysis of nucleic acid sequences support the monophyly of the cyanobacteria and actinobacteria but no

83 Analyses support the monophyly of the Cyanobacteria, alphabetagamma-Proteobac

84 Other nif analyses resolve and support the monophyly of the cyanobacteria, proteobacteria, and acti

85 The debate centers on the placement and monophyly of the cyanobacteria, proteobacteria, and Gram

86 We also examined the monophyly of the group considered as the eggplant relati

87 Systematic conclusions support the monophyly of the infraorder Pecora, the monophyly of the

88 The monophyly of the major subgroups of Copepoda, including

89 netic studies on mtDNA have shown reciprocal monophyly of the matrilines among seven of the nine assu

90 ar phylogeny provided strong support for the monophyly of the Mucorales, exclusive of Echinosporangiu

91 Cervinae and confirm for the first time the monophyly of the Old World Capreolinae (including the Ch

92 monophyly of the Acantharea and the separate monophyly of the Polycystinea (Spumellarida) are well su

93 Phylogenetic analysis supports the monophyly of the Ptolemaiida, including Kelba, and recov

94 logy-based phylogenetic analyses support the monophyly of the Scalidophora (Kinorhyncha, Loricifera,

95 the monophyly of the infraorder Pecora, the monophyly of the subfamily Bovinae (containing the Bosel

96 genetic analysis of these sequences supports monophyly of the two Hawaiian genera but, surprisingly,

97 evidence for convergence of the orb web, the monophyly of the two typical orb web taxa, the cribellat

98 e) within the Xag that strongly supports the monophyly of the Xag.

99 ow an early-branching position of Noctiluca, monophyly of thecate (plate-bearing) dinoflagellates, an

100 nucleotide and amino-acid sequence indicate monophyly of these talitrid taxa.

101 e traditional morphology-based taxonomy; the monophyly of three of four major groups is rejected.

102 s of 37 spider fibroin sequences support the monophyly of TuSp1 within the spider fibroin gene family

103 some basal felids, but does not support the monophyly of various saber-toothed tribes and genera.

104 orphisms, we identify strong support for the monophyly of, and subsequent sympatric divergence within

105 ld eliminate shared polymorphism, leading to monophyly or exclusivity of populations, when the elapse

106 strongly indicates that the ancestor of this monophyly originated by a de novo fusion of a kinase gen

107 ior, including the maintenance of nontrivial monophyly probabilities for gene lineage samples that sp

108 cies tree topology and branch lengths on the monophyly probability.

109 random, under 3 different models of expected monophyly rates: approximately 63% of 425 surveyed morph

110 e approach, we find an emerging signal of RG monophyly (supported by approximately 50% of the examine

111 or other approaches dependent on population monophyly, they provide important insights into the hist

112 Hesperiinae formed a clade, but support for monophyly was weak.

113 nal; conflicting, strong support for tineoid monophyly when synonymous signal was added back is shown

114 The monophyly with haptophytes is robustly recovered in the

115 omesticated crops appear to be associated by monophyly with only a single geographic locality.

116 described non-bioluminescent strains exhibit monophyly within the V. fischeri clade.