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275 results for “Morpho”
FIGURES 129B–140 in Poecilimon bosphoricus group (Orthoptera, Phaneropterinae): iteration of morpho-taxonomy by song characteristics 3225
FIGURES 129B–140. Photos of female ovipositor (scale = 2 mm): 29—P. bosphoricus (Turkey: A-Istanbul, B-Bolu, C- Çankırı, D-Kastamonu), 130—P. bidens (Turkey: Kocaeli), 131—P. istanbul (Turkey: Istanbul), 132—P. miramae (Turkey: Sakarya), 133—P. roseoviridis sp.n. (Bulgaria—Strandzha Mts), 134—P. similis (Turkey: Rize), 135—P. bischoffi (Turkey: Rize), 136—P. scythicus (Ukraine: Crimea), 137—P. tauricus (=P. ajpetri syn.n. —Ukraine: Crimea), 138—P. tauricus (=P. kusnezovi syn.n.) (Ukraine: Crimea), 139—P. pliginskii (Ukraine: Crimea), 140—P. pliginskii (=P. boldyrevi syn.n.) (Ukraine: Crimea).
FIGURES 141–150 in Poecilimon bosphoricus group (Orthoptera, Phaneropterinae): iteration of morpho-taxonomy by song characteristics 3225
FIGURES 141–150. Female subgenital plate and basal valves of the ovipositor (scale = 1 mm): 141—P. sureyanus (=P. anatolicus syn.n. and P. diversus syn. n.) (Turkey: A-Bilecik; B-Bursa, C-Balıkesir), 142—P. kocaki (Turkey: Sakarya), 143— P. turcicus (Turkey: Edirne), 144— P. heinrichi (Bulgaria: Strandzha) 145—P. cervus (Turkey: Bolu), 146— P. demirsoyi (Turkey: A, B-Bolu), 147— P. bosphoricus, (Turkey: A, B-Bolu, C-Kastamonu), 148—P. bidens (Turkey: Kocaeli), 149—P. istanbul (Turkey: Istanbul), 150—P. miramae (Turkey: A, B-Sakarya).
FIGURES 115–121 in Poecilimon bosphoricus group (Orthoptera, Phaneropterinae): iteration of morpho-taxonomy by song characteristics 3225
FIGURES 115–121. Photos of male subgenital plate (scale = 2 mm): 115—P. bosphoricus (Turkey: A, B, C-Istanbul, D, E- Bolu, F, G-Çankırı), 116—P. bidens (Turkey: A-Istanbul, B-Kocaeli), 117—P. istanbul (Turkey: Istanbul), 118—P. miramae (Turkey: A-paratype B-Sinop, C-Sakarya), 119—P. roseoviridis sp.n. (Bulgaria: Strandzha Mts), 120—P. similis (Turkey: A- Rize, B-Art-vin, Russia: C-Krasnaya Polyana, Ukraine: D-Crimea), 121—P. bischoffi (Turkey: A, B-Rize).
FIGURES 23–25 in Poecilimon bosphoricus group (Orthoptera, Phaneropterinae): iteration of morpho-taxonomy by song characteristics 3225
FIGURES 23–25. Photos of male pronotum, from above (scale = 2 mm): 23—P. sureyanus (= P. anatolicus syn.n. and P. diversus syn. n.) (Turkey: A, B, C-Bilecik, D, E-Bursa, F, G-Balıkesir, H-Greece: Lekomi), 24—P. kocaki (Turkey: Sakarya), 25—P. turcicus (Tukey: A-Edirne, B-Balıkesir, Greece: C-Mytillini).
FIGURES 77B-81 in Poecilimon bosphoricus group (Orthoptera, Phaneropterinae): iteration of morpho-taxonomy by song characteristics 3225
FIGURES 77B-81. Hand drawings of male cerci (scale = 1 mm): 77—P. bischoffi (Turkey: A, B-Trabzon, Ukraine: C-Crimea) 78—P. scythicus (Ukraine: A-Donetsk, B, C, D-Ramme 1951), 79—P. tauricus (Ukraine: A, B, C-Crimea, D, E, F, G- Ramme 1951), 80—P. tauricus (=P. kusnezovi syn.n. and P. beybienkoi) (A, B, C, D, E, F, G-Ukraine: Crimea, H-Ramme 1933), 81—P. pliginskii (Ukraine: A—Crimea) (=P. boldyrevi syn.n. —Krasnolesje) (Ukraine: B, C, D, E-Crimea).
FIGURES 15–22 in Poecilimon bosphoricus group (Orthoptera, Phaneropterinae): iteration of morpho-taxonomy by song characteristics 3225
FIGURES 15–22. Hand drawings of male pronotum, from above (scale = 2 mm): 15—P. miramae (Bulgaria: Rhodopian Mts.), 16—P. roseoviridis sp. n. (Bulgaria: Strandzha), 17—P. similis (Turkey: Rize), 18—P. bischoffi (Turkey: A-Trab-zon, Ukraine: B-Crimea), 19—P. scythicus (Ukraine: Crimea), 20—P. tauricus (Ukraine: A, B-Crimea), 21—P. tauricus (= P. kusnezovi syn.n.) (Ukraine: A, B-Crimea), 22—P. pliginskii (Ukraine: A, B-Crimea) (=P. boldyrevi syn.n. Krasnolesje) (Ukraine: C, D-Crimea).
FIGURES 2–4 in Poecilimon bosphoricus group (Orthoptera, Phaneropterinae): iteration of morpho-taxonomy by song characteristics 3225
FIGURES 2–4. Terminology followed in this study. 2—male pronotum (A—P. heinrichi, B—P. bosphoricus), 3—Male cerci (A—P. heinrichi, B—P. naskrecki, C-P. bosphoricus), 4—Male anal tergum (A—P. pliginskii, B, C—P. tauricus), 5—Male subgenital plate (P. sureyanus).
FIGURES 31D–36E in Poecilimon bosphoricus group (Orthoptera, Phaneropterinae): iteration of morpho-taxonomy by song characteristics 3225
FIGURES 31D–36E. Hand drawings of male pronotum, from above (scale = 2 mm): 31—P. bosphoricus (Turkey: A, B— Istanbul, C-Bolu, D-Kastamonu), 32—P. bidens (Turkey: Istanbul), 33—P. istanbul (Turkey: Istanbul), 34—P. miramae (Turkey: A-holotypus, B, C-Sakarya), 35—P. roseoviridis (Bulgaria: Strandzha), 36—P. similis (Turkey: A-Rize, B-Artvin, C- Ordu, Georgia: D, E- Bakuriani, Russia).
FIGURE 11 in Morpho (Morpho) helenor (Cramer) (Lepidoptera, Nymphalidae, Morphinae) in Bolivia: Geographical distribution and ecological plasticity, with a description of a new subspecies
FIGURE 11. Morpho helenor, intermediate coelestis-theodorus phenotype, from San Francisco, Chapare (a, b), and Morpho helenor prometa, paratype from quebrada Alarachi, Tarija (c,d).
FIGURE 9 in Morpho (Morpho) helenor (Cramer) (Lepidoptera, Nymphalidae, Morphinae) in Bolivia: Geographical distribution and ecological plasticity, with a description of a new subspecies
FIGURE 9. Map of Southern Yungas ecoregion, showing the ecosystems where Morpho helenor prometa has been collected.
FIGURE 3 in Morpho (Morpho) helenor (Cramer) (Lepidoptera, Nymphalidae, Morphinae) in Bolivia: Geographical distribution and ecological plasticity, with a description of a new subspecies
FIGURE 3. Bolivian ecoregions (http://www.worldwildlife.org/science/ecoregions/terrestrial.cfm) with localities where Morpho helenor specimens have been collected.
FIGURE 2 in Morpho-phylogenetic evidence reveals Lasiodiplodia chiangraiensis sp. nov. (Botryosphaeriaceae) associated with woody hosts in northern Thailand
FIGURE 2. Lasiodiplodia chiangraiensis (MFLU 21-0003, holotype). a–c. Conidiomata on host surface. d. Section through conidiomata. e. Peridium. f. Ostiolar region with periphyses. g. Paraphyses. h–k. Conidia developing on conidiogenous cells. l–o. Hyaline, aseptate conidia. p. Germinating conidium. q, r. Colonies after 7 days on PDA (q from above, r from below). Scale bars: b = 500 μm, c = 200 μm, d–e = 10 μm, f = 20 μm, g–p = 10 μm.
FIGURE 1 in Morpho-phylogenetic evidence reveals Lasiodiplodia chiangraiensis sp. nov. (Botryosphaeriaceae) associated with woody hosts in northern Thailand
FIGURE 1. Phylogenetic tree generated from maximum parsimony (MP) analysis based on combined ITS, tef and tub2 sequence data of Lasiodiplodia. Bootstrap values for maximum likelihood (ML) and maximum parsimony (MP) equal to or greater than 75% are placed above and below the branches, respectively. Branches with Bayesian posterior probabilities (BYPP) equal or greater than 0.95 are thickened. The new isolates are indicated in red and ex-type strains are in bold. The tree is rooted to Diplodia mutila (CMW 7060) and D. seriata (CBS 112555). The scale bar shows 20 changes.
FIGURE 8 in Adaptive morpho-traits, taxonomy and biogeography of Metania Gray, 1867 (Porifera: Spongillina: Metaniidae) with the description of a new species from Madagascar
FIGURE 8. Metania madagascariensis sp. nov. Holotype MSNG 57788 from the Matsiatra River. Gemmule architecture (SEM). A-B. Gemmule without gemmular cage; foramen with conical tubule and simple collar surrounded by distal tips of some rows of gemmuloscleres (B detail of A); C-D. Gemmule with gemmular cage of stout, smooth megascleres; foramen with simple collar surrounded by distal tips of gemmuloscleres (D detail of C); E-F. Gemmular surface covered by skeletal microscleres (spiny oxeas); microscleres on gemmular surface (F detail of E); G. gemmular theca with the fibrous pneumatic layer (cross section) and short foraminal tube; H. magnification of the trilayered gemmular theca with outer layer armed by gemmuloscleres distal tips, fibrous pneumatic layer with a monolayer of radially embedded tubelliform gemmuloscleres, and sublayered inner layer of compact spongin.
FIGURE 7 in Adaptive morpho-traits, taxonomy and biogeography of Metania Gray, 1867 (Porifera: Spongillina: Metaniidae) with the description of a new species from Madagascar
FIGURE 7. Metania madagascariensis sp. nov. Holotype MSNG 57788 from the Matsiatra River. A. Tubelliform (trumpetlike) gemmuloscleres; B. acanthoxea (microscleres) entirely ornamented by dense spines (LM). Megascleres are not represented.
FIGURE 3. A in Adaptive morpho-traits, taxonomy and biogeography of Metania Gray, 1867 (Porifera: Spongillina: Metaniidae) with the description of a new species from Madagascar
FIGURE 3. A. Map with first record of the genus Metania from Madagascar with type locality of Metania madagascariensis sp. nov. in the central Madagascan highland indicated by a black/white circle (21°25'36.1092"S, 47°9'23.7054"E); B-C. Different satellite magnifications of the type locality under a bridge of the River Matsiatra (Upper Basin of Mangoky River), crossing the Highway (R.N.) n°7 between Fianarantsoa (7.7 Km) and Ambalakely (1.5 Km) in the Haute-Matsiatra Region.
FIGURE 10 in Adaptive morpho-traits, taxonomy and biogeography of Metania Gray, 1867 (Porifera: Spongillina: Metaniidae) with the description of a new species from Madagascar
FIGURE 10. Schema of relevant morpho-traits divergences of gemmular theca architecture at the genus level in the family Metaniidae. Spatial arrangement of gemmuloscleres (left) and layers of the theca (right): 1) outer layer; 2) pneumatic layer; 3) inner layer. In Corvomeyenia the pneumatic layer is shifted from its usual position i.e. not in contact with the inner layer and overlapping the distal tips of the radially arranged birotules. In Metania and Acalle sharing the same trilayered gemmular architecture the pneumatic layer fill the entire space between radial gemmuloscleres (boletiform in Acalle vs. tubelliform in Metania); moreover the Acalle gemmules are ornate by supplementary pseudobirotules in the outer layer. In Houssayella and Drulia the pneumatic layer is lost. The gemmuloscleres of Houssayella (Trochospongilla-like birotules) are radially embedded in the two resting theca layers. The single-rotule gemmuloscleres (parmuliform) of Drulia are laid directly on the gemmular surface or pluristratified and embedded in the two resting layers of the theca. Not to scale.
FIGURE 9 in Adaptive morpho-traits, taxonomy and biogeography of Metania Gray, 1867 (Porifera: Spongillina: Metaniidae) with the description of a new species from Madagascar
FIGURE 9. Hypothesized evolutionary trend of gemmuloscleres in four genera of the Metaniidae family: pseudobirotules (left) to tubelliform, boletiform (middle) and parmuliform (right) (modified from Volkmer-Ribeiro, 1986).
FIGURE 2 in Adaptive morpho-traits, taxonomy and biogeography of Metania Gray, 1867 (Porifera: Spongillina: Metaniidae) with the description of a new species from Madagascar
FIGURE 2. Genus Metania. Spicular complements of the 11 hitherto accepted Metania species plus the new species M. madagascariensis sp. nov.(modified in part from Volkmer-Ribeiro, 1979, 1986; Volkmer-Ribeiro & Costa, 1992, 1993).
FIGURE 1 in Adaptive morpho-traits, taxonomy and biogeography of Metania Gray, 1867 (Porifera: Spongillina: Metaniidae) with the description of a new species from Madagascar
FIGURE 1. Worldwide geographic range of the genus Metania suggesting a Gondwanan biogeographic pattern with all circumtropical-equatorial records in the Neotropical, Afrotropical, Oriental, and Australian Regions. Each dot refers to one or more species.
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