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291 results for “Ecological diversification”

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Fig. 141 in Mammals Of The Rio Juruá And The Evolutionary And Ecological Diversification Of Amazonia

Fig. 141. Shape and depth of the mesopterygoid fossa in the eight species of Proechimys that occur within the Rio Juruá basin. (Top) from left to right: P. brevicauda (MNFS 1325, locality 1); P. cuvieri (JLP 15310, locality 7); P. echinothrix (JUR 377, locality 15); P. gardneri (MVZ 187206, locality 9). (Bottom) from left to right: P. pattoni (MVZ 187195, locality 1); P. kulinae (MVZ 187186, locality 6); P. simonsi (JLP 15296, locality 7); and P. steerei (MNFS 595, locality 5).

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Fig. 148 in Mammals Of The Rio Juruá And The Evolutionary And Ecological Diversification Of Amazonia

Fig. 148. (Left) Map of the distribution of Proechimys simonsi (modified from Patton, 1987) illustrating localities for which 801 bp of cytochrome­b sequence are available, lettered or numbered as in the tree (right). Localities belonging to each of the two mtDNA clades are encompassed by ellipses (Right) Strict­consensus maximum parsimony tree of five equally minimum­length trees for 20 individual haplotypes from 15 localities in Peru´, Bolivia, and Brazil, as identified in the map (left). Length = 498 steps; CI = 0.677; RI = 0.588. Sequences of other species of Proechimys and of Mesomys were used to root the tree. Bold numbers at internal nodes are bootstrap values, based on 1000 replicates percentages are average Kimura two­parameter distances. Voucher catalog numbers and localities for each haplotype are given in table 71.

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Fig. 165 in Mammals Of The Rio Juruá And The Evolutionary And Ecological Diversification Of Amazonia

Fig. 165. Sample localities and distribution of haplotypes of the cytochrome­b gene for the pygmy rice rat Oligoryzomys microtis (above) and rice rat Oryzomys megacephalus (below) along the Rio Jurua´. Single haplotypes shared among localities are indicated by ellipses connecting them. The number of haplotypes unique to each locality is also indicated.

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Fig. 138 in Mammals Of The Rio Juruá And The Evolutionary And Ecological Diversification Of Amazonia

Fig. 138. Dorsal views of the skulls of the eight species of Proechimys that occur within the Rio Juruá basin. (Top) from left to right: P. brevicauda (MNFS 1121, locality 1), P. cuvieri (JLP 15310 locality 7), P. echinothrix (MVZ 187182, locality 14), P. gardneri (MVZ 187209, locality 9). (Bottom from left to right: P. kulinae (MPEG 25502, locality 6), P. pattoni (MVZ 187194, locality 1), P. simonsi (MNFS 1441, locality 4), P. steerei (JLP 15700, locality 6). Natural size.

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Fig. 139 in Mammals Of The Rio Juruá And The Evolutionary And Ecological Diversification Of Amazonia

Fig. 139. Ventral views of the skulls of the eight species of Proechimys that occur within the Rio Juruá basin. (Top) from left to right: P. brevicauda (MNFS 1121, locality 1), P. cuvieri (JLP 15310 locality 7), P. echinothrix (MVZ 187182, locality 14), P. gardneri (MVZ 187209, locality 9). (Bottom) from left to right: P. kulinae (MPEG 25502, locality 6), P. pattoni (MVZ 187194, locality 1), P. simonsi (MNFS 1441, locality 4), P. steerei (JLP 15700, locality 6). Natural size.

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Fig. 140 in Mammals Of The Rio Juruá And The Evolutionary And Ecological Diversification Of Amazonia

Fig. 140. Shape and structure of the incisive foramina of the eight species of Proechimys that occur within the Rio Juruá basin. (Top) from left to right: P. brevicauda (MNFS 1325, locality 1); P. cuvieri (JLP 15310, locality 7); P. echinothrix (JUR 377, locality 15); P. gardneri (MVZ 187203, locality 9). (Bottom) from left to right: P. pattoni (MVZ 187197, locality 4); P. kulinae (MVZ 187186, locality 6); P. simonsi (JLP 15539, locality 6); and P. steerei (MNFS 595, locality 5).

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Fig. 136 in Mammals Of The Rio Juruá And The Evolutionary And Ecological Diversification Of Amazonia

Fig. 136. Bivariate plots of the first two discriminant axes in separate analyses of two triads of species of Proechimys from the Rio Jurua´ (top) P. brevicauda, P. cuvieri, and P. echinothrix; (bottom) P. gardneri, P. kulinae, and P. pattoni.

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Fig. 144 in Mammals Of The Rio Juruá And The Evolutionary And Ecological Diversification Of Amazonia

Fig. 144. (Above) Map of the distribution of Proechimys cuvieri (modified from Patton, 1987) Localities from which individual specimens have been examined for sequence of the mtDNA cytochrome­b gene are indicated; those from localities outside of the Rio Juruá are lettered. Regionally monophyletic clades, identified in the tree below, are circumscribed by solid lines. (Below) Bootstrap consensus minimum­length parsimony tree for haplotypes of the mitochondrial cytochrome­b gene (798 bp); length = 351 steps, CI = 0.721, RI = 0.779. Sequences of other species of Proechimys and of Mesomys were used as outgroups to root the tree. Bold numbers at internal nodes are bootstrap values based on 1000 replicates; percentages are average Kimura two­parameter distances. Voucher catalog

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Fig. 135 in Mammals Of The Rio Juruá And The Evolutionary And Ecological Diversification Of Amazonia

Fig. 135. (Top) Bivariate plots of the first two discriminant axes comparing morphometric relationships among the eight species of Proechimys obtained from the Rio Jurua´. (Bottom, left) Histograms with 95% confidence limits, of individual scores on the first discriminant axis. (Bottom, right) Histograms, with 95% confidence limits, of individual scores on the second discriminant axis.

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Fig. 137 in Mammals Of The Rio Juruá And The Evolutionary And Ecological Diversification Of Amazonia

Fig. 137. Outlines of representative bacula of each of the eight species of Proechimys that occur within the Rio Juruá basin.

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Fig. 134. Bootstrap 50 in Mammals Of The Rio Juruá And The Evolutionary And Ecological Diversification Of Amazonia

Fig. 134. Bootstrap 50% majority­rule consensus minimum­length parsimony tree for cytochrome­b haplotypes (798 bp) for the eight species of Proechimys from the Rio Jurua´. The tree is based on a weighted analysis that discounted third­position transitions (see text for explanation). The terminal triangles encompass the individual haplotypes of each species included in the analysis, the number of which is indicated within each triangle. The tree is rooted by comparison to Isothrix, Makalata, and Mesomys. Length = 351 steps, CI = 0.721, RI = 0.779. Bold numbers at internal nodes are bootstrap values, based on 1000 replicates; percentages are average Kimura twoparameter distances.

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Fig. 133 in Mammals Of The Rio Juruá And The Evolutionary And Ecological Diversification Of Amazonia

Fig. 133. Distribution of eight species of Proechimys at the 16 primary sample sites along the Rio Jurua´, western Brazil.

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Fig. 132 in Mammals Of The Rio Juruá And The Evolutionary And Ecological Diversification Of Amazonia

Fig. 132. Distribution of discriminant scores on the single axis obtained in a comparison of cranial measurements for the upriver and downriver cytochrome­b clades of Mesomys hispidus.

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Fig. 160 in Mammals Of The Rio Juruá And The Evolutionary And Ecological Diversification Of Amazonia

Fig. 160. Phenogram of Jaccard's similarity coefficients in comparisons of species composition between all documented species of marsupials, murid rodents, and echimyid rodents from each of the 16 primary sample sites along the Rio Jurua´. Terminal branches are identified by locality number (see map, fig. 1); hatched boxes at basal nodes represent 95% confidence limits. Mantel's matrix correlation coefficient for the association between the similarity matrix and the cophenetic correlation matrix is 0.873, p <0.001.

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Fig. 131 in Mammals Of The Rio Juruá And The Evolutionary And Ecological Diversification Of Amazonia

Fig. 131. Distribution of discriminant scores on the single axis obtained in a comparison of cranial measurements of Mesomys occultus and M. hispidus.

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Fig. 167 in Mammals Of The Rio Juruá And The Evolutionary And Ecological Diversification Of Amazonia

Fig. 167. (A) A maximum­likelihood tree of 47 cytochrome­b haplotypes of the terrestrial spiny rat, Proechimys simonsi, recovered from 150 individuals from 11 localities along the Rio Jurua´. (B) A maximum­likelihood tree of 48 cytochrome­b haplotypes of the terrestrial spiny rat, Proechimys steerei, recovered from 205 individuals from 13 localities along the Rio Jurua´. The locality (or localities) and river bank (R = right, L = left) for each haplotype are indicated. The solid circles indicate cases where individual haplotypes had to be transferred across the river given these particular tree topologies; those in a terminal position represent single haplotypes presently found on both banks, those at internal nodes hypothesize historical transfers to account for the genealogical distribution.

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Fig. 163 in Mammals Of The Rio Juruá And The Evolutionary And Ecological Diversification Of Amazonia

Fig. 163. The relationship between average sequence divergence (Kimura two­parameter distances for the mitochondrial cytochrome­b gene and the relative degree of phylogeographic partitioning in 30 species or species pairs of nonvolant mammals of the Rio Juruá (following Avise et al., 1987). A high degree of phylogeographic structure indicates that haplotype lineages are confined to particular sections along the river, either left versus right bank or some pattern of regional partitioning. Medium structure is when some haplotype lineages are confined to single geographic areas while others are not. Finally low or no structure characterizes those taxa where there is no relationship between haplotype lineages and geography. The four phylogeographic categories of Avise et al. (1987; Avise, 1989) are indicated with Roman numerals.

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Fig. 155 in Mammals Of The Rio Juruá And The Evolutionary And Ecological Diversification Of Amazonia

Fig. 155. Bivariate plots of the first and second principal components axes (top, left) and second and third principal components axes (top, right) illustrating the morphometric relationships between samples of Proechimys steerei by geographic regions along the Rio Jurua´. (Bottom) Plot of the first and second principal components axes in comparisons between samples of P. steerei on opposite river banks of the Rio Jurua´.

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Fig. 152 in Mammals Of The Rio Juruá And The Evolutionary And Ecological Diversification Of Amazonia

Fig. 152. Bivariate relationship between morphometric distance (Mahalanobis D2; above) and genetic similarity (Slatkin's [1993] M­statistic below) and the log of the straight­line geographic distance between sample localities of Proechimys simonsi along the Rio Jurua´. Mantel's matrix correlation coefficients and their significance are indicated for each.

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Fig. 145 in Mammals Of The Rio Juruá And The Evolutionary And Ecological Diversification Of Amazonia

Fig. 145. (Above) Map of the distribution of Proechimys echinothrix (modified from da Silva, 1998 illustrating localities for which 801 bp of cytochrome­b sequence are available, lettered or numbered as in the tree (bottom). Localities belonging to each of the three mtDNA clades are encompassed by ellipses. (Below) Single most parsimonious tree generated by the branch­and­bound procedure for 18 individual haplotypes from the eight localities in the map (top). Length = 341 steps; CI = 0.757; RI = 0.872. Sequences of other species of Proechimys and of Mesomys were used to root the tree. Bold numbers at internal nodes are bootstrap values, based on 1000 replicates; percentages are average Kimura two­parameter distances. Voucher catalog numbers and localities for each haplotype are given in table 69.

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