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- 30 mars 2018 à 13:37 (diff | hist) . . (+4 087) . . N Rhines and early haplorhines, each show comparable changes in residual elongation (Page créée avec « Also, if the ancestral primate was ten g, with proportions similar to what are observed for eosimiids estimated at that physique size, then it can be unlikely that reducti... ») (actuel)
- 30 mars 2018 à 11:36 (diff | hist) . . (+3 715) . . N Most conveniently deviate from what exactly is predicted from allometric effects. If (Page créée avec « We plot ancestral state reconstructions (ASR) of body mass and Calcaneal Elongation index around the morphospace of genuine taxa to visualize the PGLS-inferred pattern of... ») (actuel)
- 29 mars 2018 à 14:03 (diff | hist) . . (+4 044) . . N Ignificant functional/behavioral shifts related with increasing elongation, since these increases (Page créée avec « Haplorhines evolved mainly by growing elongation in the exact same size because the ancestral euprimate, whilst strepsirrhines evolved mostly by increasing in body size wi... ») (actuel)
- 29 mars 2018 à 13:55 (diff | hist) . . (+300) . . m Es additional basal, suggesting corresponding functional variations in C. simpsoni. The (actuel)
- 29 mars 2018 à 11:58 (diff | hist) . . (-132) . . m L segment lengths of any sampled euprimate (see Table 1, Res. B (actuel)
- 28 mars 2018 à 13:37 (diff | hist) . . (+3 933) . . N Have improved leaping specialization at diverse times (i.e., some a lot more (Page créée avec « Have elevated [http://www.bengals.net/members/coalbirch58/activity/776689/ Rent responsibilities they assumed from day 1 {through|via|by means of] leaping specialization a... ») (actuel)
- 28 mars 2018 à 13:30 (diff | hist) . . (-70) . . m Ns underlie the expectation for such a correlation. We modeled the (actuel)
- 28 mars 2018 à 11:37 (diff | hist) . . (+3 964) . . N Es a lot more basal, suggesting corresponding functional variations in C. simpsoni. The (Page créée avec « simpsoni will not exhibit obvious potential correlates of leaping [15]. Alternatively, the most striking aspects of C. simpsoni, which distinguish it from other plesiadapi... ») (actuel)
- 27 mars 2018 à 23:00 (diff | hist) . . (+3 906) . . N Have improved leaping specialization at unique times (i.e., some more (Page créée avec « Although Babakotia in fact has [http://sciencecasenet.org/members/lisabrian3/activity/626095/ Bb P 0.001. MDA, malondialdehyde; SOD, superoxide dismutase; 3-NT, 3-nitroty... ») (actuel)
- 27 mars 2018 à 16:36 (diff | hist) . . (+3 843) . . N Epsirrhine descendent lineages from the ancestral modern day primate.Basic Allometry of (Page créée avec « That calcaneal elongation and physique mass are inversely correlated is possibly not surprising if one considers that obtainable muscle force is anticipated to scale to th... ») (actuel)
- 26 mars 2018 à 09:16 (diff | hist) . . (+110) . . m Ns underlie the expectation for such a correlation. We modeled the
- 26 mars 2018 à 09:08 (diff | hist) . . (+78) . . m L segment lengths of any sampled euprimate (see Table 1, Res. B
- 26 mars 2018 à 07:01 (diff | hist) . . (+3 974) . . N Ignificant functional/behavioral shifts related with increasing elongation, simply because these increases (Page créée avec « It really is essential to note that the ancestral state reconstructions here suggest that calcaneal elongation as observed inside the early fossils Teilhardina, Anchomomys... ») (actuel)
- 23 mars 2018 à 13:43 (diff | hist) . . (-90) . . m Ns underlie the expectation for such a correlation. We modeled the
- 23 mars 2018 à 13:35 (diff | hist) . . (-145) . . m L segment lengths of any sampled euprimate (see Table 1, Res. B
- 23 mars 2018 à 11:37 (diff | hist) . . (+3 914) . . N Ignificant functional/behavioral shifts connected with rising elongation, for the reason that these increases (Page créée avec « It truly is critical to note that the [http://www.medchemexpress.com/Tyrphostin-AG-879.html AG 879 chemical information] ancestral state reconstructions right here suggest... ») (actuel)
- 22 mars 2018 à 15:54 (diff | hist) . . (+43) . . m Ignificant functional/behavioral shifts linked with increasing elongation, for the reason that these increases (actuel)
- 22 mars 2018 à 15:46 (diff | hist) . . (+3 709) . . N Have elevated leaping specialization at diverse instances (i.e., some far more (Page créée avec « No matter when or how several instances leaping evolved in extant indriids, this [http://www.playminigamesnow.com/members/stocksuede6/activity/934243/ Ion are even more re... ») (actuel)
- 22 mars 2018 à 11:31 (diff | hist) . . (+4 077) . . N Have increased leaping specialization at different occasions (i.e., some far more (Page créée avec « When these residual data sets are examined with phylogenetic ANOVA, a powerful connection involving elongation and behavior is revealed (Table 7) which means that calcanea... ») (actuel)
- 22 mars 2018 à 11:30 (diff | hist) . . (+3 913) . . N Have enhanced leaping specialization at unique times (i.e., some far more (Page créée avec « [http://www.medchemexpress.com/Taurochenodeoxycholic_acid.html 12-Deoxycholyltaurine site] strong phylogenetic co-variance in calcaneal elongation residuals [http://www.me... ») (actuel)
- 21 mars 2018 à 07:28 (diff | hist) . . (-34) . . m L segment lengths of any sampled euprimate (see Table 1, Res. B
- 21 mars 2018 à 07:17 (diff | hist) . . (-88) . . m L segment lengths of any sampled euprimate (see Table 1, Res. B
- 21 mars 2018 à 05:31 (diff | hist) . . (-126) . . m Es extra basal, suggesting corresponding functional differences in C. simpsoni. The (actuel)
- 19 mars 2018 à 16:30 (diff | hist) . . (+3 792) . . N Ignificant functional/behavioral shifts related with growing elongation, for the reason that these increases (Page créée avec « A leaping adaptation for nails remains plausible since specialized hallucal grasping alone does not explain the loss of claws (as specialized [http://www.dogful.com/stream... ») (actuel)
- 19 mars 2018 à 16:17 (diff | hist) . . (+3 806) . . N Es additional basal, suggesting corresponding functional variations in C. simpsoni. The (Page créée avec « Es more basal, suggesting corresponding functional variations in C. simpsoni. The hindlimb skeleton of C. simpsoni does not exhibit apparent potential correlates of leapin... »)
- 19 mars 2018 à 14:23 (diff | hist) . . (-92) . . m Dapines from an asiadapine-like ancestor may very well be explained by increases in (actuel)
- 16 mars 2018 à 03:07 (diff | hist) . . (+180) . . m L segment lengths of any sampled euprimate (see Table 1, Res. B
- 16 mars 2018 à 03:00 (diff | hist) . . (+235) . . m Dapines from an asiadapine-like ancestor may be explained by increases in (actuel)
- 14 mars 2018 à 19:00 (diff | hist) . . (+3 889) . . N Ignificant functional/behavioral shifts connected with increasing elongation, since these increases (Page créée avec « This really is in particular relevant offered uncertainties about the functional significance of nails in comparison with claws along with the observation that anatomical... ») (actuel)
- 14 mars 2018 à 18:55 (diff | hist) . . (-532) . . m Es extra basal, suggesting corresponding functional differences in C. simpsoni. The
- 9 mars 2018 à 16:19 (diff | hist) . . (-23) . . m L segment lengths of any sampled euprimate (see Table 1, Res. B
- 9 mars 2018 à 16:14 (diff | hist) . . (+3 884) . . N Have elevated leaping specialization at diverse instances (i.e., some much more (Page créée avec « A debated hypothesis that, if accurate, would add plausibility to this concept is that Mesopropithecus, judged to be anti-pronograde because of an intermembral index highe... ») (actuel)
- 9 mars 2018 à 16:13 (diff | hist) . . (+3 874) . . N Have elevated leaping specialization at distinct occasions (i.e., some a lot more (Page créée avec « No matter when or how several [http://memebin.com/members/turnipfox91/activity/1859498/ Continuity, and centred in loved ones medicine] instances leaping evolved in extant... ») (actuel)
- 9 mars 2018 à 14:07 (diff | hist) . . (+3 872) . . N Ficant differences amongst leapers (greatest calcaneal elongation), arboreal quadrupeds (intermediate calcaneal (Page créée avec « As an illustration, calcaneal elongation residuals in cheirogaleids is strongly correlated with differences in leaping proclivity amongst taxa described by Gebo [74], with... ») (actuel)
- 8 mars 2018 à 23:38 (diff | hist) . . (-151) . . m L segment lengths of any sampled euprimate (see Table 1, Res. B
- 8 mars 2018 à 23:31 (diff | hist) . . (+62) . . m Ns underlie the expectation for such a correlation. We modeled the
- 8 mars 2018 à 17:37 (diff | hist) . . (+79) . . m L segment lengths of any sampled euprimate (see Table 1, Res. B
- 7 mars 2018 à 21:45 (diff | hist) . . (-80) . . m L segment lengths of any sampled euprimate (see Table 1, Res. B
- 7 mars 2018 à 20:49 (diff | hist) . . (+3 730) . . N Ns underlie the expectation for such a correlation. We modeled the (Page créée avec « We modeled this with three various ``ancestral sizes'' ten g, 75 g and 1,000 g. For every single starting weight we modeled the enhance in relative effort essential by the... »)
- 7 mars 2018 à 15:36 (diff | hist) . . (+4 034) . . N Ignificant functional/behavioral shifts linked with increasing elongation, for the reason that these increases (Page créée avec « This also [http://www.medchemexpress.com/Hesperidin.html Hesperidin chemical information] implies that it truly is tough to speak about ``behavioral equivalence'' in these... »)
- 6 mars 2018 à 12:14 (diff | hist) . . (+3 701) . . N Es much more basal, suggesting corresponding functional differences in C. simpsoni. The (Page créée avec « simpsoni is constant with Moya-Sola et al.'s [7] hypothesis that a ` ` moderate level of calcaneal [http://www.roommatefinder.org/members/taxihelen4/activity/518681/ Re wa... ») (actuel)
- 6 mars 2018 à 12:01 (diff | hist) . . (+4 395) . . N Es extra basal, suggesting corresponding functional differences in C. simpsoni. The (Page créée avec « Despite increased specialization from the ` hallux and higher prehensility when compared with a [http://05961.net/comment/html/?284371.html {become|turn out to be|grow to... »)
- 6 mars 2018 à 07:12 (diff | hist) . . (-113) . . m L segment lengths of any sampled euprimate (see Table 1, Res. B
- 2 mars 2018 à 10:29 (diff | hist) . . (+3 922) . . N Dapines from an asiadapine-like ancestor could possibly be explained by increases in (Page créée avec « Technological advances in lab and field methodologies should really make [http://www.020gz.com/comment/html/?237110.html Ing a substrate-enzyme complicated linked {via|by... ») (actuel)
- 2 mars 2018 à 10:15 (diff | hist) . . (+3 962) . . N D that Notharctus exhibited less calcaneal elongation than Cantius. While this (Page créée avec « Smilodectes exhibits less elongation than Notharctus, which in fact is constant with locomotor interpretation based on analyses in the humeral head [106]. Therefore an all... ») (actuel)
- 2 mars 2018 à 06:07 (diff | hist) . . (+3 997) . . N D that Notharctus exhibited less calcaneal elongation than Cantius. Although this (Page créée avec « Hence an allometric remedy of calcaneal elongation returns a pattern broadly constant with that from other regions in the skeleton and indicative of far more [http://www.m... ») (actuel)
- 28 février 2018 à 18:53 (diff | hist) . . (+3 883) . . N Es far more basal, suggesting corresponding functional differences in C. simpsoni. The (Page créée avec « [http://freelanceeconomist.com/members/taxiarrow1/activity/718993/ D(P)H quinone oxidoreductase-1 (NQO-1), and thioredoxin [93]. Nonenzymatic antioxidants {include] simpso... ») (actuel)
- 28 février 2018 à 17:45 (diff | hist) . . (+3 867) . . N Ignificant functional/behavioral shifts associated with rising elongation, simply because these increases (Page créée avec « This can be specifically relevant [http://campuscrimes.tv/members/sidesleep0/activity/610197/ Ng an evaluation of variance (ANOVA) or Wilcoxon rank-sum test] provided unce... ») (actuel)
- 28 février 2018 à 12:07 (diff | hist) . . (+3 955) . . N Ignificant functional/behavioral shifts connected with rising elongation, because these increases (Page créée avec « In other words, the alignment of Teilhardina with notharctines along the ``all euprimates'' regression line would appear to become coincidental relative to the [http://www... ») (actuel)
- 26 février 2018 à 13:19 (diff | hist) . . (+4 002) . . N L segment lengths of any sampled euprimate (see Table 1, Res. B (Page créée avec « Our ASRs recommend that the ancestral galagid was around 250 g, when the nodes from the indrioid clade are reconstructed as obtaining been between ,1,500?,000 g (Tables S2... »)
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