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Distribution. Endemic to S India (Kolar district, Karnataka), known only from type locality. Previously also on nearby Therahalli, where now absent. in Hipposideridae
Distribution. Endemic to S India (Kolar district, Karnataka), known only from type locality. Previously also on nearby Therahalli, where now absent.
Distribution. Endemic to Laos, known only from type locality and Ban Nampe, C.I1 km NE of Vang Vieng, Vang Vieng district, Vientiane Province in Hipposideridae
Distribution. Endemic to Laos, known only from type locality and Ban Nampe, C.I1 km NE of Vang Vieng, Vang Vieng district, Vientiane Province
FIGURE 2 in Catalog of type specimens of the fish collection of the Núcleo de Pesquisas em Limnologia, Ictiologia e Aquicultura (NUP), Universidade Estadual de Maringá Paraná, Brazil
FIGURE 2. Distribution of the richness of fish species by orders and by river basins across the Neotropical region, deposited as type-material in the NUP fish collection.
FIGURE 1 in Catalog of type specimens of the fish collection of the Núcleo de Pesquisas em Limnologia, Ictiologia e Aquicultura (NUP), Universidade Estadual de Maringá Paraná, Brazil
FIGURE 1. Richness of species by order and family, deposited as type-material in the NUP fish collection.
Distribution. Discontinuous and limited to wetland environments in two areas of S Sudan: small swamps in SW Sudan near the DR Congo border, where the type specimen was collected, and the Sudd Swamps (Bahr-el-Ghazal) of the upper White Nile. Maps and distributional information here are provisional pending future research. in Bovidae
Distribution. Discontinuous and limited to wetland environments in two areas of S Sudan: small swamps in SW Sudan near the DR Congo border, where the type specimen was collected, and the Sudd Swamps (Bahr-el-Ghazal) of the upper White Nile. Maps and distributional information here are provisional pending future research.
Data from: Plant functional types broadly describe water use strategies in the Caatinga, a seasonally dry tropical forest in northeast Brazil
<ol> <li><span>In seasonally dry tropical forests, plant functional type can be classified as deciduous low wood density, deciduous high wood density, or evergreen high wood density species. While deciduousness is often associated with drought-avoidance and low wood density is often associated with tissue water storage, the degree to which these functional types may correspond to diverging and unique water use strategies has not been extensively tested. </span></li> <li><span>We examined (1) tolerance to water stress, measured by pre-dawn and mid-day leaf water potential; (2) water use efficiency, measured via foliar δ<sup>13</sup>C; and (3) access to soil water,<i> </i>measured via stem water δ<sup>18</sup>O.</span></li> <li><span>We found that deciduous low wood density species maintain high leaf water potential and low water use efficiency. Deciduous high wood density species have lower leaf water potential and variable water use efficiency. Both groups rely on shallow soil water. Evergreen high wood density species have low<i> </i>leaf water potential, higher water use efficiency, and access alternative water sources. These findings indicate that deciduous low wood density species are drought avoiders, with a specialized strategy for storing root and stem water. Deciduous high wood density species are moderately drought tolerant, and evergreen high wood density species are the most drought tolerant group. </span></li> <li><span><i>Synthesis. </i>Our results broadly support the plant functional type framework as a way to understand water use strategies, but also highlight species-level differences. </span></li> </ol>
FIGURES 6–10 in An undescribed species among Roesler's type specimens: Ancylosis palianytsia sp nov. (Lepidoptera: Pyralidae: Phycitinae) described from Afghanistan
FIGURES 6–10. Head structures of Ancylosis spp. Ancylosis palianytsia sp. nov.: 6–7. Antennae (6. Paratype, Sarobi, Prep. no. ♀629.22s; 7. Paratype, Gulbahar, Prep. no. ♂632.22g). 9–10. Labial palpi (9. Paratype, Gulbahar, Prep. no. ♀341.20s; 10. Holotype, Sarobi, Prep. no. ♂630.22s). Ancylosis monella: 8a. Antennae, 8b. Labial palpi (Paratype, Polihomri, Prep. no. ♂342.20s).
FIGURES 4–5 in An undescribed species among Roesler's type specimens: Ancylosis palianytsia sp nov. (Lepidoptera: Pyralidae: Phycitinae) described from Afghanistan
FIGURES 4–5. Females of Ancylosis palianytsia sp. nov. 4. Paratype, Gulbahar, Prep. no. ♀341.20s. 5. Paratype, Sarobi, Prep. no. ♀629.22s. Scale bar: 10 mm.
FIGURES 14–15 in An undescribed species among Roesler's type specimens: Ancylosis palianytsia sp nov. (Lepidoptera: Pyralidae: Phycitinae) described from Afghanistan
FIGURES 14–15. Female genitalia of Ancylosis palianytsia sp. nov. 14. Paratype, Gulbahar, Prep. no. ♀341.20s. 15. Paratype, Sarobi, Prep. no. ♀629.22s. Scale bar: 1 mm.
FIGURES 11–13 in An undescribed species among Roesler's type specimens: Ancylosis palianytsia sp nov. (Lepidoptera: Pyralidae: Phycitinae) described from Afghanistan
FIGURES 11–13. Male genitalia of Ancylosis palianytsia sp. nov. 11. Ventral view, aedeagus apart (a), aedeagus (b), culcita (c), juxta (d) (Paratype, Gulbahar, Prep. no. ♂631.22s.). 12. Ventral view, aedeagus apart (a), aedeagus (b), culcita (c), juxta (d), right valva (e), left valva (f) (Holotype, Sarobi, Prep. no. ♂630.22s.). 13. Gnathos, lateral view (a), right valva (b) (Paratype, Gulbahar, Prep. no. ♂632.22g.). Scale bar: 1 mm.
FIGURES 10–15 in Types of the New World Stigmoderini (Coleoptera: Buprestidae) deposited in Finnish Museum of Natural History, Helsinki (Buprestidae: Buprestinae: Stigmoderini)
FIGURES 10–15. Lectotypes of Hiperantha spp., dorsal and lateral views, and labels; 10–12) Hyperantha menetriesii (specimen http://id.luomus.fi/GAC.33084); 13–15) Hyperantha sanguinosa (specimen http://id.luomus.fi/GAC.33085). Photographs by Pekka Malinen.
FIGURES 1–9 in Types of the New World Stigmoderini (Coleoptera: Buprestidae) deposited in Finnish Museum of Natural History, Helsinki (Buprestidae: Buprestinae: Stigmoderini)
FIGURES 1–9. Lectotypes of Conognatha spp., dorsal and lateral views, and labels; 1–3) Stigmodera auricollis (specimen http://id.luomus.fi/GAC.24384); 4–6) Stigmodera carinata (specimen http://id.luomus.fi/GAC.24385); 7–9) Stigmodera lebasii (specimen http://id.luomus.fi/GAC.24386). Photographs by Pekka Malinen.
FIGURES 16–18 in Types of the New World Stigmoderini (Coleoptera: Buprestidae) deposited in Finnish Museum of Natural History, Helsinki (Buprestidae: Buprestinae: Stigmoderini)
FIGURES 16–18. Lectotype of Lasionota quadrifasciata (specimen http://id.luomus.fi/GL.674); 16) Dorsal view; 17) Antennae; 18) Labels. Photographs by Pekka Malinen.
FIGURE 12 in Morphological types of male copulatory organs of Bicornucythere bisanensis (Ostracoda, Crustacea) and the description of a new Bicornucythere species
FIGURE 12. Bicornucythere misumiensis sp. nov. Internal lateral views of male carapace of left (A) and right (B) valves, respectively (SUM-CO-2505, paratype). Arrows indicate anterior. Scale: 100 µm.
FIGURE 11 in Morphological types of male copulatory organs of Bicornucythere bisanensis (Ostracoda, Crustacea) and the description of a new Bicornucythere species
FIGURE 11. Exposed soft parts and pore systems of Bicornucythere misumiensis sp. nov. A and B, soft parts of female and male, respectively. C–E, male left copulatory organ (ventral view). C, whole image; D, extension of the distal lobe; E, tip of the distal lobe. F, maxillula of male. G–J, pore systems. G and H, corolla-like pore (reported by Okada, 1982 as a Ben-type pore). I, broom-shape seta (black arrow). J, simple seta. A, SUM-CO-2510, paratype; B–F, SUM-CO-2511, paratype; G–J, SUM-CO-2508, paratype. Arrows indicate anterior (A and B). Scale: 100 μm for A and B, 50 μm for C, 30 μm for F, 20 μm for D, 10 μm for I, 2 μm for E and J, 1 μm for G and H.
FIGURE 9 in Morphological types of male copulatory organs of Bicornucythere bisanensis (Ostracoda, Crustacea) and the description of a new Bicornucythere species
FIGURE 9. Appendages of Bicornucythere misumiensis sp. nov. A, antennule. B, antenna. C, mandibula. D, maxillula. E, male right 5th limb. E1, segment boundary in male right 5th limb. E2, faint segment boundary in male right 5th limb. F, female right 5th limb. G, left 5th limb. H, 6th limb. I, 7th limb. J, brush-shaped organ. K, left furca. A, C, J, K SUM-CO-2501, male holotype; B, E, G–I, L, M, SUM-CO-2502, male paratype; D, SUM-CO-2503, paratype; B, F, SUM-CO-2504, female paratype. Scale: 100 μm for A-K, 125 μm for E1, E2.
FIGURE 8 in Morphological types of male copulatory organs of Bicornucythere bisanensis (Ostracoda, Crustacea) and the description of a new Bicornucythere species
FIGURE 8. Male copulatory organs of Bicornucythere misumiensis sp. nov. (SUM-CO-2501, holotype). ca, clasping apparatus; cd, copulatory duct; dl, distal lobe. Scale: 100 μm.
FIGURE 5 in Morphological types of male copulatory organs of Bicornucythere bisanensis (Ostracoda, Crustacea) and the description of a new Bicornucythere species
FIGURE 5. Size distribution of male carapace of Bicornucythere species. Circles = Bicornucythere bisanensis from Aburatsubo Cove; Rhombuses = Bicornucythere bisanensis from Ushimad; Squares = Bicornucythere bisanensis from Misumi-cho; Triangles = B. misumiensis sp. nov. from Misumi-cho.
FIGURE 4 in Morphological types of male copulatory organs of Bicornucythere bisanensis (Ostracoda, Crustacea) and the description of a new Bicornucythere species
FIGURE 4. Diagram of the four Types of male copulatory organs identified in the Aburatsubo Cove samples. Each Type consists of a combination of right and left distal lobes that is, R, r, L, and l.
FIGURE 6 in Morphological types of male copulatory organs of Bicornucythere bisanensis (Ostracoda, Crustacea) and the description of a new Bicornucythere species
FIGURE 6. Morphological variation in the extension degree of the tip of Shape r in Type D and difference from Shape R in Type A. A, specimens from Aburatsubo Cove. B, specimens from Ushimado. The Aburatsubo Cove samples included some specimens from Shape R group, and they were distinguished from Shape r samples based on their elongated sub-triangular outline and tapering curved tip, which differed from the spindle-shaped outline and pointed tip observed in Shape r samples. Each number correlates with a specific specimen from each locality.
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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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