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FIGURE 2. Approximate distribution maps for species from 11 in Systematics of the blindsnakes (Serpentes: Scolecophidia: Typhlopoidea) based on molecular and morphological evidence
FIGURE 2. Approximate distribution maps for species from 11 of 19 typhlopoid genera; Amerotyphlops, Xenotyphlopidae (Xenotyphlops), Gerrhopilidae (Gerrhopilus), Typhlops, Rhinotyphlops, Anilios, Xerotyphlops, Indotyphlops, Madatyphlops, Argyrophis, and Malayotyphlops. Seven other genera are pictured in Figure 4. Note that I. braminus has an essentially cosmopolitan distribution, and is not factored into the range for Indotyphlops (see Wallach 2009 for a recent summary of known localities).
FIGURE 1. Results from a in Systematics of the blindsnakes (Serpentes: Scolecophidia: Typhlopoidea) based on molecular and morphological evidence
FIGURE 1. Results from a molecular phylogenetic analysis of 95 of the 275 known, extant species of typhlopoid blindsnakes. Tree represents the ML estimate from a concatenated matrix of 4 mitochondrial and 6 nuclear genes (6290bp total), inferred using 200 independent searches in RAxMLv7.2.8, with support estimated from 1000 non-parametric BS replicates (>50% shown).
FIGURE 3. Approximate distribution maps for species from 7 in Systematics of the blindsnakes (Serpentes: Scolecophidia: Typhlopoidea) based on molecular and morphological evidence
FIGURE 3. Approximate distribution maps for species from 7 of 19 typhlopoid genera: Grypotyphlops, Letheobia, Lemuriatyphlops, Cyclotyphlops, Acutotyphlops, Afrotyphlops, and Ramphotyphlops.
FIGURE 4 in First record of the African-Indian centipede genus Digitipes Attems, 1930 (Scolopendromorpha: Otostigminae) from Myanmar, and the systematic position of a new species based on molecular phylogenetics
FIGURE 4. Maximum likelihood consensus tree based on combined COI and 16S sequences. Numbers at nodes are bootstrap support in maximum likelihood (ML) and posterior probabilities in Bayesian inference (BI). Black circles refer to nodes supported from both ML and BI; grey circle refers to a node supported only by ML.
FIGURE 3 in First record of the African-Indian centipede genus Digitipes Attems, 1930 (Scolopendromorpha: Otostigminae) from Myanmar, and the systematic position of a new species based on molecular phylogenetics
FIGURE 3. Drawings depicting variation in some morphological characters; A. Cephalic plate and T1 (Holotype). B. Forcipular segment (Holotype). C. Tooth-plate with five teeth on right side (Paratype; CUMZ 00234). D. Articles 1–3 of telopodite of second maxilla (Paratype; CUMZ 00241). E. Tergites 9–11 (Holotype). F. Sternite 10 (Paratype; CUMZ 00240). G. Coxopleural pore area (Holotype). H. Sternite of ultimate leg-bearing segment with ultimate legs (Holotype; ventral view). I. Left ultimate leg (Paratype; CUMZ 00234).
FIGURE 2 in First record of the African-Indian centipede genus Digitipes Attems, 1930 (Scolopendromorpha: Otostigminae) from Myanmar, and the systematic position of a new species based on molecular phylogenetics
FIGURE 2. Morphological characters of Digitipes kalewaensis n. sp.; A. Forcipular coxosternite (Paratype; CUMZ 00234). B- C. Tergites and sternites 9–11 (Paratype; CUMZ 00241). D. Antenna, cephalic plate and T1 (Holotype). E-G. Spiracles 3, 5 and 8, respectively (Holotype). H, J. Ultimate legs (Paratypes; CUMZ 00234-00235). I. Projection on femur of ultimate leg in male (Holotype). K. Pore-field of coxopleuron (left and right; Paratype; CUMZ 00235). L-M. Ventral and dorsal view of ultimate leg-bearing segment (Paratype; CUMZ 00234).
FIGURE 1 in First record of the African-Indian centipede genus Digitipes Attems, 1930 (Scolopendromorpha: Otostigminae) from Myanmar, and the systematic position of a new species based on molecular phylogenetics
FIGURE 1. Collecting area of Digitipes kalewaensis n. sp.; A. Location of collection area in Myanmar. B. Collecting locality (expanded magnification). C. Habitat type.
FIGURE 12 in Raising Thalictrum uncatum var. angustialatum (Ranunculaceae) from China to T. angustialatum as an independent species based on evidence from morphology, geographical distribution, cytology and molecular systematics
FIGURE 12. Specimens of Thalictrum angustialatum (previously misidentified as T. leuconotum). A. China, Sichuan, Muli, Muli Exped. 52 (SM704604658); inset: flower. B. China, Sichuan, Muli, T.T. Yu 5706 (KUN0689917); inset: flower. C. China, Sichuan, Puge, Sichuan Med. Plant Exped. 25061 (SM704604653); inset: aggregate fruit. D. China, Sichuan, Xide, Anonymous 295 (SM704604657); inset: aggregate fruit.
FIGURE 11 in Raising Thalictrum uncatum var. angustialatum (Ranunculaceae) from China to T. angustialatum as an independent species based on evidence from morphology, geographical distribution, cytology and molecular systematics
FIGURE 11. Specimens of Thalictrum angustialatum (previously misidentified as T. uncatum). A. China, Sichuan, Meigu, Anonymous 13088 (PE01040627); inset: aggregate fruit. B. China, Sichuan, Meigu, Anonymous 13126 (PE00427839); inset: aggregate fruit. C. China, Sichuan, Zhaojue, Anonymous 12823 (CDBI0026391); inset: aggregate fruit. D. China, Sichuan, Zhaojue, Anonymous 12823 (PE00427838); inset: aggregate fruit.
FIGURE 10. A specimen numbered Bijie Exped. 125 in Raising Thalictrum uncatum var. angustialatum (Ranunculaceae) from China to T. angustialatum as an independent species based on evidence from morphology, geographical distribution, cytology and molecular systematics
FIGURE 10. A specimen numbered Bijie Exped. 125 (PE00471121) and agreeing with other sheets of Bijie Exped. 125 in the collection records, but actually belonging to Thalictrum lecoyeri and not cited in the protologue of T. angustialatum, and thus not an isotype of T. angustialatum.
FIGURE 9 in Raising Thalictrum uncatum var. angustialatum (Ranunculaceae) from China to T. angustialatum as an independent species based on evidence from morphology, geographical distribution, cytology and molecular systematics
FIGURE 9. Mitotic metaphase chromosomes of Thalictrum angustialatum (A) (2n = 28), T. leuconotum (B, C) (2n = 14), T. sinomacrostigma (D) (2n = 28), and T. uncatum (E‒I) (2n = 14), all same scale. A. China, Yunnan, Qiaojia, Y.P. Zeng & Q.L. Huang 315 (IBSC). B. China, Sichuan, Wenchuan, Y.P. Zeng & Q.L. Huang 344 (IBSC). C. China, Xizang, Yadong, L. Wang et al. 2952 (IBSC). D. China, Sichuan, Kangding, Y.P. Zeng & Q.L. Huang 373 (IBSC). E. China, Sichuan, Litang, Y.P. Zeng & Q.L. Huang 403 (IBSC). F. China, Xizang, Bomi, W.Q. Fei 57 (IBSC). G. China, Xizang, Qamdo, L. Wang et al. 3410 (IBSC). H. China, Xizang, Nangxian, L. Wang et al. 3210 (IBSC). I. China, Xizang, Riwoqe, L. Wang et al. 3452 (IBSC).
FIGURE 8 in Raising Thalictrum uncatum var. angustialatum (Ranunculaceae) from China to T. angustialatum as an independent species based on evidence from morphology, geographical distribution, cytology and molecular systematics
FIGURE 8. Distribution of Thalictrum angustialatum (■) and T. uncatum (●). Arrow indicates the type locality of T. angustialatum, i.e. Weining in Guizhou, China.
FIGURE 7 in Raising Thalictrum uncatum var. angustialatum (Ranunculaceae) from China to T. angustialatum as an independent species based on evidence from morphology, geographical distribution, cytology and molecular systematics
FIGURE 7. Sepals (A, E), stamens (B, F), carpels (C, G), and achenes (D, H) in Thalictrum angustialatum (A‒D) and T. uncatum (E‒H).
FIGURE 5 in Raising Thalictrum uncatum var. angustialatum (Ranunculaceae) from China to T. angustialatum as an independent species based on evidence from morphology, geographical distribution, cytology and molecular systematics
FIGURE 5. Thalictrum sinomacrostigma in the wild (Kangding in Sichuan, China). A. Habitat. B. Habit (plant in flowering). C. Habit (plant in fruiting). D. Roots. E. Portion of stem. F. Leaf (left: adaxial side; right: abaxial side; inset: stipels). G. Leaflet (left: adaxial side; right: abaxial side). H. Flower. I. Sepal (left: abaxial side; right: adaxial side). J. Stamens. K. Carpels. L. Aggregate fruit. M. Achenes (immature). Photographed by Y.P. Zeng.
FIGURE 6 in Raising Thalictrum uncatum var. angustialatum (Ranunculaceae) from China to T. angustialatum as an independent species based on evidence from morphology, geographical distribution, cytology and molecular systematics
FIGURE 6. Thalictrum uncatum in the wild (Kangding in Sichuan, China). A. Habitat. B. Habit (plant in flowering). C. Habit (plant in fruiting). D. Roots. E. Portion of stem. F. Leaf (left: adaxial side; right: abaxial side; inset: stipels). G. Leaflet (left: adaxial side; right: abaxial side). H. Flower. I. Sepal (left: abaxial side; right: adaxial side). J. Stamens. K. Carpels. L. Aggregate fruit. M. Achenes (immature). Photographed by Y.P. Zeng.
FIGURE 4 in Raising Thalictrum uncatum var. angustialatum (Ranunculaceae) from China to T. angustialatum as an independent species based on evidence from morphology, geographical distribution, cytology and molecular systematics
FIGURE 4. Thalictrum leuconotum in the wild (A, B, D‒K: Wenchuan in Sichuan, China; C, L, M: Yadong in Xizang, China). A. Habitat. B. Habit (plant in flowering). C. Habit (plant in fruiting). D. Roots. E. Portion of stem. F. Leaf (left: adaxial side; right: abaxial side; inset: stipels). G. Leaflet (left: adaxial side; right: abaxial side). H. Flower. I. Sepal (left: abaxial side; right: adaxial side). J. Stamens. K. Carpels. L. Aggregate fruit. M. Achenes (immature). Photographed by Y.P. Zeng.
FIGURE 3 in Raising Thalictrum uncatum var. angustialatum (Ranunculaceae) from China to T. angustialatum as an independent species based on evidence from morphology, geographical distribution, cytology and molecular systematics
FIGURE 3. Specimens of Thalictrum angustialatum. A‒D: China, Yunnan, Qiaojia, Y.P. Zeng & Q.L. Huang 315 (IBSC).
FIGURE 2 in Raising Thalictrum uncatum var. angustialatum (Ranunculaceae) from China to T. angustialatum as an independent species based on evidence from morphology, geographical distribution, cytology and molecular systematics
FIGURE 2. Thalictrum angustialatum in the wild (Qiaojia in Yunnan, China). A. Habitat. B. Habit (plant in flowering). C. Habit (plant in fruiting). D. Roots. E. Portion of stem. F. Leaf (left: adaxial side; right: abaxial side; inset: stipels). G. Leaflet (left: adaxial side; right: abaxial side). H. Flower. I. Sepal (left: abaxial side; right: adaxial side). J. Stamens. K. Carpels. L. Aggregate fruit. M. Achenes (immature). Photographed by Y.P. Zeng.
FIGURE 7 in Molecular Systematics of Redband Trout from Genome-Wide DNA Sequencing Substantiates the Description of a New Taxon (Salmonidae: Oncorhynchus mykiss calisulat) from the McCloud River
FIGURE 7. Phylogenetic network of individuals examined in this study produced by the neighbor net algorithm. Tips are labeled by individual codes described in Table 1. Each subspecies of Rainbow Trout (Oncorhynchus mykiss) is indicated. McCloud River Redband Trout (O. m. calisulat, ssp. nov.) and Sacramento River Redband Trout (O. m. stonei) are show in bold. The outgroup species, Lahontan Cutthroat Trout (O. clarkii henshawi) is indicated.
FIGURE 3 in Molecular Systematics of Redband Trout from Genome-Wide DNA Sequencing Substantiates the Description of a New Taxon (Salmonidae: Oncorhynchus mykiss calisulat) from the McCloud River
FIGURE 3. Admixture plots from the population genetics data set. Number of genetic clusters (K) presented for K = 2–6 from all samples (n = 318) analyzed in a population genetics framework. Admixture analysis was conducted in NGSAdmix with an optimal K = 3. Labeling of x-axis is according to Group as in Table 1: CAGT, California Golden Trout; KRRT, Kern River Rainbow Trout; LKGT, Little Kern Golden Trout; CRT, Coastal Rainbow Trout; EGLK, Eagle Lake Rainbow Trout; HRNB, Hatchery Rainbow Trout; MRRB, McCloud River Redband Trout; REDB, all other Redband Trout.
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Allen Brain Atlas
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International Brain Laboratory public data
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OpenNeuro
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