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FIGURE 16. Licea pygmaea and L. pusilla spore size. For each specimen indicated 30 in Species of Licea Schrad. (Myxomycetes) in Kedrovaya Pad State Nature Biosphere Reserve (Far East, Russia), including two new species
FIGURE 16. Licea pygmaea and L. pusilla spore size. For each specimen indicated 30 spores were measured.
FIGURE. Blades of C. spongifolia. A. Sub-marginal and marginal collective veins, with laminal tissue (2–4 mm) between. B. Marginal collective veins fused below shallow sinus. C. Underside with spongy appearance produced by "false pores"; and thick, rubbery texture indicated by axial wrinkles formed in crease. D. Underside showing primary vein and pinnate lateral veins surrounded by spongy tissue. E. Sub-stomatal cavities revealed by transmitted light (scale unit 0.25 mm), F. Sub-stomatal cavities revealed by removing lower epidermis (A–D: Mengla County, 2018. E–F: Bach Ma NP seedling, ex situ). Photos: PJM. in Colocasia spongifolia sp. nov. (Araceae) in southern China and central Vietnam
FIGURE. Blades of C. spongifolia. A. Sub-marginal and marginal collective veins, with laminal tissue (2–4 mm) between. B. Marginal collective veins fused below shallow sinus. C. Underside with spongy appearance produced by "false pores"; and thick, rubbery texture indicated by axial wrinkles formed in crease. D. Underside showing primary vein and pinnate lateral veins surrounded by spongy tissue. E. Sub-stomatal cavities revealed by transmitted light (scale unit 0.25 mm), F. Sub-stomatal cavities revealed by removing lower epidermis (A–D: Mengla County, 2018. E–F: Bach Ma NP seedling, ex situ). Photos: PJM.
Subspecies and Distribution. M.a.auriculusBR.H.Baker&Stains,1955-EsideofSierraMadreOrientalfromNuevoLeonintoTamaulipasandVeracruz(Mexico). M. a. apache Hoffmeister & Krutzsch, 1955 — from the mountains of SE Arizona and SW New Mexico (USA) S to Jalisco (Mexico); also in N Coahuila (Mexico). There is a record from Guatemala, but geographic discontinuity and absence of new records in almost 40 years indicates need for taxonomic revision ofthis specimen. in Vespertilionidae
Subspecies and Distribution. M.a.auriculusBR.H.Baker&Stains,1955-EsideofSierraMadreOrientalfromNuevoLeonintoTamaulipasandVeracruz(Mexico). M. a. apache Hoffmeister & Krutzsch, 1955 — from the mountains of SE Arizona and SW New Mexico (USA) S to Jalisco (Mexico); also in N Coahuila (Mexico). There is a record from Guatemala, but geographic discontinuity and absence of new records in almost 40 years indicates need for taxonomic revision ofthis specimen.
Distribution. Confirmed from NW Africa, the Sahel, and Nile Valley, E through the Middle East and WArabia to NW& C India (E to E Madhya Pradesh, 80° E); with possible distribution spots in E & SE India (indicated byfour mostlyhistorical records). Reportedly common in Bangladesh (yet disproved by recent reports) and retained on species lists of Myanmar, Thailand, and Sumatra without being supported by anyrecent record. in Rhinopomatidae
Distribution. Confirmed from NW Africa, the Sahel, and Nile Valley, E through the Middle East and WArabia to NW& C India (E to E Madhya Pradesh, 80° E); with possible distribution spots in E & SE India (indicated byfour mostlyhistorical records). Reportedly common in Bangladesh (yet disproved by recent reports) and retained on species lists of Myanmar, Thailand, and Sumatra without being supported by anyrecent record.
FIGURE 7 in Intraspecific variations of morphometric indices of some species of the genus Ditylenchus Filipjev, 1936 (Nematoda: Anguinidae) in relation to diet and temperature
FIGURE 7. Lateral fields (A-C) and tail shape variations (D-I). A. Four lateral lines in Ditylenchus dipsaci; B. Six lateral lines in D. myceliophagus; C. Additional lines between main lines in D. destructor; D. Pointed tail terminus in male of D. destructor; E. Thick tail with rounded terminus in D. myceliophagus; F. Thin tail with pointed terminus in D. medicaginis; G & H. Finely rounded tail terminus in D. geraerti and D. destructor; I. Mucronate tail terminus in D. parvus. All scale-bars = 10 µm.
FIGURE 6 in Intraspecific variations of morphometric indices of some species of the genus Ditylenchus Filipjev, 1936 (Nematoda: Anguinidae) in relation to diet and temperature
FIGURE 6. Effect of different temperature treatments on means of morphometric indices of pure population of Ditylenchus myceliophagus. Bars with the same letter(s) are not significantly different (P <0.05), according to Duncan's Multiple Range Test.
FIGURE 5 in Intraspecific variations of morphometric indices of some species of the genus Ditylenchus Filipjev, 1936 (Nematoda: Anguinidae) in relation to diet and temperature
FIGURE 5. Effect of different temperature treatments on means of morphometric indices of pure populations of Ditylenchus dipsaci (Garlic and alfalfa populations). In each population, bars with the same letter(s) are not significantly different (P <0.05), according to Duncan's Multiple Range Test.
FIGURE 3 in Intraspecific variations of morphometric indices of some species of the genus Ditylenchus Filipjev, 1936 (Nematoda: Anguinidae) in relation to diet and temperature
FIGURE 3. Effect of different diet treatments on means of morphometric indices of pure population of Ditylenchus myceliophagus. Bars with the same letter(s) are not significantly different (P <0.05), according to Duncan's Multiple Range Test.
FIGURE 4 in Intraspecific variations of morphometric indices of some species of the genus Ditylenchus Filipjev, 1936 (Nematoda: Anguinidae) in relation to diet and temperature
FIGURE 4. Effect of different temperature treatments on means of morphometric indices of pure populations of Ditylenchus destructor (Hamadan, Kerman and Fars populations; codes 188, 347 and 348, respectively). In each population, bars with the same letter(s) are not significantly different (P <0.05), according to Duncan's Multiple Range Test.
FIGURE 2 in Intraspecific variations of morphometric indices of some species of the genus Ditylenchus Filipjev, 1936 (Nematoda: Anguinidae) in relation to diet and temperature
FIGURE 2. Effect of different diet treatments on means of morphometric indices of pure populations of Ditylenchus dipsaci (Garlic and alfalfa populations). In each population, bars with the same letter(s) are not significantly different (P <0.05), according to Duncan's Multiple Range Test.
FIGURE 1 in Intraspecific variations of morphometric indices of some species of the genus Ditylenchus Filipjev, 1936 (Nematoda: Anguinidae) in relation to diet and temperature
FIGURE 1. Effect of different diet treatments on means of morphometric indices of pure population of Ditylenchus destructor (Hamadan population, code 188). Bars with the same letter(s) are not significantly different (P <0.05), according to Duncan's Multiple Range Test.
Figure 6. Chronogram resulting from Bayesian analysis employing a in Phylogeny indicates polyphyly in Cnodocentron (Trichoptera: Xiphocentronidae): biogeography and revision of New World species (Caenocentron)
Figure 6. Chronogram resulting from Bayesian analysis employing a relaxed clock. Most likely ancestral distribution recovered in DEC analysis and estimated mean age are displayed at the nodes. Dispersal events are indicated as a black line below the distribution boxes, vicariant events are indicated in a green line, as recovered in the biogeographic analysis. Highest posterior density (HPD) 95% intervals for the ages of the nodes are indicated by light blue bars. Timescale and global surface temperature estimated from δ18O benthic (Zachos et al., 2001) are displayed on the bottom. Eocene and Miocene thermal optimum are highlighted in grey. Cnodocentron and Caenocentron species distributions are shown in the maps.
Figure 5. Maximum credibility Bayesian tree obtained from 46 in Phylogeny indicates polyphyly in Cnodocentron (Trichoptera: Xiphocentronidae): biogeography and revision of New World species (Caenocentron)
Figure 5. Maximum credibility Bayesian tree obtained from 46 morphological characters and COI coded to Cnodocentron sensu Schmid and related taxa (all compatible groups shown). Morphological character states are displayed along the branches: boxes refer to unambiguous transformations; circles to characters under ACCTRAN optimization. Black symbols indicate unique character changes. Posterior probability support values are displayed in boxes below the node branches. Male genitalia of species of each clade are displayed in lateral view. Oriental species modified from the original descriptions: Malicky & Chantaramongkol (1992), Oláh & Johanson (2010), Schmid (1982).
Figure 3 in Phylogeny indicates polyphyly in Cnodocentron (Trichoptera: Xiphocentronidae): biogeography and revision of New World species (Caenocentron)
Figure 3. Mesothorax: A, Caenocentron carlosdelarosai; B, Cnodocentron brogimarus; C, Xiphocentron maiteae; D, Melanotrichia samaconius. Hind leg apical spur: E, Drepanocentron sp.; F, Cnodocentron sp.
Figure 2 in Phylogeny indicates polyphyly in Cnodocentron (Trichoptera: Xiphocentronidae): biogeography and revision of New World species (Caenocentron)
Figure 2. Wing venation: A, Melanotrichia attia; B, Cnodocentron tchaturbhuja; C, Cnodocentron girika. Male genitalia: D, aspect of mesal sclerite of Melanotrichia sp., 200×; E, Melanotrichia attia, lateral view; F, Cnodocentron vrisaparvan, lateral view. Male genitalia, sternum IX, ventral: G, Cnodocentron filamenta; H, Cnodocentron brogimarus; I, Cnodocentron tchaturbhuja; J, Cnodocentron devayani; K, Cnodocentron vrisaparvan; L, Cnodocentron girika. Female genitalia, segment VIII apex, dorsal: M, Caenocentron carlosdelarosai; N, Cnodocentron tchaturbhuja.
Figure 13 in Phylogeny indicates polyphyly in Cnodocentron (Trichoptera: Xiphocentronidae): biogeography and revision of New World species (Caenocentron)
Figure 13. Caenocentron rafamoralesi sp. nov. A, wing venation. Male genitalia: B, lateral; C, dorsal; D, ventral.
Figure 1 in Phylogeny indicates polyphyly in Cnodocentron (Trichoptera: Xiphocentronidae): biogeography and revision of New World species (Caenocentron)
Figure 1. Xiphocentronidae world distribution showing Cnodocentron sensu Schmid species distribution in red circles. Tropical moist forests are displayed in green.
Figure 12 in Phylogeny indicates polyphyly in Cnodocentron (Trichoptera: Xiphocentronidae): biogeography and revision of New World species (Caenocentron)
Figure 12. Bayesian analysis of COI sequences of Caenocentron carlosdelarosai and Caenocentron rafamoralesi and other xiphocentronids, showing clustering associating male and females of each species. COI accession numbers are displayed in front of each specimen. Posterior probability values are displayed below each node.
Figure 4. A in Phylogeny indicates polyphyly in Cnodocentron (Trichoptera: Xiphocentronidae): biogeography and revision of New World species (Caenocentron)
Figure 4. A, wing pattern of Caenocentron trilineatum. B, sternum V of C. carlosdelarosai showing reticulate cuticular plate at 200×. C, abdomen of C. carlosdelarosai, 80×. D, sternum V of Melanotrichia samaconius.
Figure 21 in Phylogeny indicates polyphyly in Cnodocentron (Trichoptera: Xiphocentronidae): biogeography and revision of New World species (Caenocentron)
Figure 21. Paleogeography of South-East Asia and Mesoamerica: A, South-East Asia, showing the collision of Indian Plate and Asia. B, Mesoamerica showing the southward movement of Chortis Block. Dispersal and vicariant events with their respective mean ages are displayed as arrows and dotted lines, respectively. Montane regions are in dark grey. Whitish regions indicate progressive seasonal dry climates after the Middle Miocene. Palaeogeographic reconstructions of Mesoamerica modified from Keppie & Moán-Zenteno (2005) and interpreted from evidence presented by Kirby et al. (2008), Coates et al. (2004) and Montes et al. (2012). Reconstructions of South-East Asia modified after Morley (2018) and Gorin et al. (2020).
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