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47 results for “Cryptocephalus”
FIGURE 95 in Taxonomic remarks, phylogeny and evolutionary notes on the leaf beetle species belonging to the Cryptocephalus sericeus complex (Coleoptera: Chrysomelidae: Cryptocephalinae)
FIGURE 95. Bayesian analysis of a morphological and molecular (central portion of the small subunit ribosomial RNA genes) combined dataset implemented for the taxa of which both types of data were available. For the molecular partition the analysis was conducted by using the general time reversible model (Lanave et al., 1984; Tavaré, 1986; Rodríguez et al., 1990) assuming rates to vary across sites according to a gamma distribution (Yang, 1994) with a proportion of invariable sites (Gu et al., 1995). For the morphological partition the analysis was conducted by using the Mk model for morphological data (Lewis, 2001). Values near branches are the bayesian posterior probabilities.
FIGURES 51–58 in Taxonomic remarks, phylogeny and evolutionary notes on the leaf beetle species belonging to the Cryptocephalus sericeus complex (Coleoptera: Chrysomelidae: Cryptocephalinae)
FIGURES 51–58. Third endophallic sclerite in dorsal view: (51): C. castilianus (Cuenca, Spain); (52): C. hypochaeridis (Vall d'Aran, Spain); (53): C. falzonii (Piani di Aspromonte, Italy); (54): C. virens (Mt. Slavnik, Slovenia); (55): C. v. scaffaiolus (Ordesa, Spain); (56): C. barii (Mt. Grigna, Italy); (57): C. rugicollis (San Giusto, Sardinia); (58): C. azurescens (Oukaimeden, Morocco). Numbers indicate characters and states. Not drawn to the same scale.
FIGURES 40–50 in Taxonomic remarks, phylogeny and evolutionary notes on the leaf beetle species belonging to the Cryptocephalus sericeus complex (Coleoptera: Chrysomelidae: Cryptocephalinae)
FIGURES 40–50. Second endophallic sclerite in ventral and (b) dorsal view: (40): C. castilianus (Cuenca, Spain); (41): C. v. violaceus (Maiz, Hungary); (42): C. v. violaceus (Iti, Greece); (43): C. leonhardi (Fonte Cerreto, Italy); (44): C. asturiensis (Pic d'Anie, France); (45): C. therondi (St. Pons, France); (46): C. therondi (St. Martin Vesubie, France); (47): C. rugicollis (San Giusto, Sardinia); (48): C. barii (Mt. Grigna, Italy); (49): C. atrifrons (Madone d'Utelle, France); (50): C. azurescens (Oukaimeden, Morocco). Numbers indicate characters and states. Not drawn to the same scale.
FIGURES 18–23 in Taxonomic remarks, phylogeny and evolutionary notes on the leaf beetle species belonging to the Cryptocephalus sericeus complex (Coleoptera: Chrysomelidae: Cryptocephalinae)
FIGURES 18–23. Median lobe of aedeagus, apex in ventral and (b) dorsal view: (18): C. transcaucasicus (Ceresole Reale, Italy); (19): C. zambanellus (Garessio, Italy); (20): C. duplicatus (Megiri, Armenia); (21): C. duplicatus (Karachaevo- Cherkessia, Russia); (22): C. barii (Mt. Presolana, Italy); (23): C. asturiensis (Pic d'Anie, France). m.l.: median lamina; f.: frenula. Numbers indicate characters and states. Not drawn to the same scale.
FIGURES 59–67 in Taxonomic remarks, phylogeny and evolutionary notes on the leaf beetle species belonging to the Cryptocephalus sericeus complex (Coleoptera: Chrysomelidae: Cryptocephalinae)
FIGURES 59–67. Fourth endophallic sclerite in dorsal view: (59): C. castilianus (Cuenca, Spain); (60): C. v. scaffaiolus (Ordesa, Spain); (61): C. virens (Rostov, Russia); (62): C. barii (Mt. Grigna, Italy); (63): C. rugicollis (Amman, Giordania); (64): C. azurescens (Oukaimeden, Morocco); (65): C. atrifrons (Madone d'Utelle, France). Tegmen: (66): C. falzonii (Orsomarso, Italy); (67): C. emiliae (Azron, Morocco). t. s.: third endophallic sclerite in anatomical connection. Numbers indicate characters and states. Not drawn to the same scale.
FIGURES 24–33 in Taxonomic remarks, phylogeny and evolutionary notes on the leaf beetle species belonging to the Cryptocephalus sericeus complex (Coleoptera: Chrysomelidae: Cryptocephalinae)
FIGURES 24–33. First endophallic sclerite in ventral view: (24): C. duplicatus (Trabzon, Turkey); (25): C. convergens (Pordoi Pass, Italy); (26): C. v. scaffaiolus (Rubiò, Spain); (27): C. v. violaceus (Iti, Greece); (28): C. virens (Zaisan Lake, Kazachstan); (29): C. leonhardi (Fonte Cerreto, Italy); (30): C. emiliae (Azrou, Morocco); (31): C. azurescens (Oukaimeden, Morocco); (32): C. barii (Mt. Grigna, Italy); (33): C. barii (Mt. Presolana, Italy). Numbers indicate characters and states. Not drawn to the same scale.
FIGURES 14–17 in Taxonomic remarks, phylogeny and evolutionary notes on the leaf beetle species belonging to the Cryptocephalus sericeus complex (Coleoptera: Chrysomelidae: Cryptocephalinae)
FIGURES 14–17. Median lobe of aedeagus, apex in ventral view: (14): C. therondi (Fontan, France); (15): C. duplicatus (Karachaevo-Cherkessia, Russia); (16): C. transcaucasicus (Vitoscha, Bulgaria) (17): C. laetus (Chelyabinsk, Russia). Numbers indicate characters and states. Not reproduced to the same scale.
FIGURES 1–4 in Taxonomic remarks, phylogeny and evolutionary notes on the leaf beetle species belonging to the Cryptocephalus sericeus complex (Coleoptera: Chrysomelidae: Cryptocephalinae)
FIGURES 1–4. (1) Aedeagus in (a) ventral, (b) dorsal, (c) lateral view: Cryptocephalus azurescens lectotype (Glaui [Telouet], Morocco). (2) Aedeagus in lateral view: (a): C. violaceus scaffaiolus (Rubiò, Spain); (b): C. v. violaceus (Val Gardena, Italy). (3) Aedeagus in ventral view, C. violaceus scaffaiolus: (a): (Rubiò, Spain); (b): (Madone d'Utelle, France). (4) Aedeagus in ventral view, C. v. violaceus: (a): (Cetinje, Montenegro); (b): (Kovacov, Slovakia). Numbers indicate characters and states. Not drawn to the same scale.
FIGURES 34–39 in Taxonomic remarks, phylogeny and evolutionary notes on the leaf beetle species belonging to the Cryptocephalus sericeus complex (Coleoptera: Chrysomelidae: Cryptocephalinae)
FIGURES 34–39. First endophallic sclerite in ventral view: (34): C. asturiensis (Pic d'Anie, France); (35): C. concolor (Astrabad, Iran); (36): C. samniticus (Genova, Italy); (37): C. cantabricus (El Escorial, Spain); (38): C. rugicollis (San Giusto, Sardinia); (39): C. laetus (South Urals, Russia). Numbers indicate characters and states. Not drawn to the same scale.
FIGURES 5–7 in Taxonomic remarks, phylogeny and evolutionary notes on the leaf beetle species belonging to the Cryptocephalus sericeus complex (Coleoptera: Chrysomelidae: Cryptocephalinae)
FIGURES 5–7. (5) Last six antennomeres: (a): C. emiliae (Azrou, Morocco); (b): C. azurescens (Oukaimeden, Morocco); (c): C. rugicollis (Cadiz, Spain); (d): C. atrifrons (Madone d'Utelle, France); (e): C. barii (Mt. Presolana, Italy); (f): C. laetus (Chelyabinsk, Russia); (g): C. regalis (Gansu, China); (h): C. leonhardi (Mt. Majella, Italy). (6) External total habitus in lateral view, schematic representation (see text for details). (7) Prosternal process: (a): C. paphlagonius (Pazaryeri, Turkey); (b): C. zambanellus (Mt. Cornizzolo, Italy). Numbers indicate characters and states. Not drawn to the same scale.
FIGURE 93 in Taxonomic remarks, phylogeny and evolutionary notes on the leaf beetle species belonging to the Cryptocephalus sericeus complex (Coleoptera: Chrysomelidae: Cryptocephalinae)
FIGURE 93. Phylogenetic relationships of C. sericeus species complex based on morphological characters only. The diagram in (a) is a majority rule (50%) consensus summarizing results from a parsimony analysis (MP) with all characters equally weighted (30 MPTs, length=125; CI = 0,51; RI = 0,84; RC = 0,43). A nearly identical topology was recovered from a Bayesian inference (BI) analysis of the same dataset using the Mk model for morphological data (Lewis, 2001). Values above branches are MP bootstrap support percentages (1000 pseudoreplicates) (left) and bayesian posterior probabilities (right), values below branches are the percentage of occurrence in the set of MTPs (left) and Decay Index (right). Only relevant values have been reported. The diagram in (b) shows the different position of C. laetus and C. regalis in a similar analysis using the iterative a posteriori characters weighting (6 MTPs, length=52.56; CI = 0,65; RI = 0,90; RC = 0,58).
FIGURES 8–13 in Taxonomic remarks, phylogeny and evolutionary notes on the leaf beetle species belonging to the Cryptocephalus sericeus complex (Coleoptera: Chrysomelidae: Cryptocephalinae)
FIGURES 8–13. Abdominal sternites: (8): C. violaceus violaceus (Titograd [Podgorica], Montenegro); (9): C. v. scaffaiolus (Lake Scaffaiolo, Italy); (10): C. sericeus (North Caucasus, Russia); (11): C. concolor (Mazendaran, Iran); (12): C. therondi (Fontan, France); (13): C. rugicollis (Azrou, Morocco). Numbers indicate characters and states. Not reproduced to the same scale.
FIGURES 78–92 in Taxonomic remarks, phylogeny and evolutionary notes on the leaf beetle species belonging to the Cryptocephalus sericeus complex (Coleoptera: Chrysomelidae: Cryptocephalinae)
FIGURES 78–92. Female rectal apparatus in ventral view: (78): C. atrifrons (Madone d'Utelle, France); (79): C. azurescens (Oukaimeden, Morocco); (80): C. emiliae (Atlas central, Morocco); (81): C. duplicatus (Amman, Jordan); (82): C. aureolus (Lillaz, France); (83): C. virens (Sarikamis, Turkey); (84): C. v. scaffaiolus (Scaffaiolo Lake, Italy); (85): C. globicollis (Pierrefeu, France). Spermatheca: (86): C. zambanellus (Verbicaro, Italy); (87): C. globicollis (Pierrefeu, France); (88): C. transiens (Crezzo, Italy); (89): C. barii (Mt. Grigna, Italy); (90): C. leonhardi (Mt. Pollino, Italy). Vaginal palp (= sternite IX): (91): C. concolor (Mazendaran, Iran); (92): C. castilianus (Riopar, Spain). a.v.s.: ventral sclerotized area. Numbers indicate characters and states. Not drawn to the same scale.
Figs. 3–5. Cryptocephalus aulicus. 3 in Comparative Morphology of the Female Genitalia and some Abdominal Structures of Neotropical Cryptocephalini (Coleoptera: Chrysomelidae: Cryptocephalinae)
Figs. 3–5. Cryptocephalus aulicus. 3) dorsal view of genitalia, tergite VIII not removed, spermatheca in the background; 4) caudal view, tergite VIII not removed; 5) caudal view, tergite VIII removed. Figs. 6–9. Cryptocephalus arizonicus. 6) tergite VIII, dorsal view; 7) dorsal view of genitalia, tergite VIII removed; 8) caudal view, tergite VIII removed; 9) spermatheca and spermathecal duct (coiled onto itself).
Figure 5 in Exploring species-level taxonomy in the Cryptocephalus flavipes species complex (Coleoptera: Chrysomelidae)
Figure 5. Newly described morphological diagnostic characters of the Cryptocephalus flavipes species complex: A, SEM micrograph of metaepisternum (scale bar 200 µm, magnification 80X); B, photographs of metaepisternum and epipleura; C, schematic drawings of metaepisternum and epipleura; D, hindleg. From top to bottom: new undescribed taxon, Cryptocephalus bameuli, Cryptocephalus flavipes, Cryptocephalus signatifrons, Cryptocephalus turcicus, Cryptocephalus quadripustulatus, and Cryptocephalus alborzensis.
Figure 4 in Exploring species-level taxonomy in the Cryptocephalus flavipes species complex (Coleoptera: Chrysomelidae)
Figure 4. Variation in the shape of the metaepisternum. Scatter plot of principal component analysis (PCA) performed on the variance–covariance matrix of the GPA shape coordinates. Principal component (PC) 1 versus PC 2 scores plot is reported; the two axes explain the 50% (PC1) and the 16.3% (PC2) of the variance. Species are identified by the symbols used in Figure 1; stars identify Cryptocephalus alborzensis. Boxes highlight individuals standing at the opposite extremes of PC1 variation; features of these specimens were reported above (negative variation) and on the right (positive variation) of the PCA scatter plot. For each individual, the following information is presented: (1) the SEM micrograph representing the metaepisternum, along with the configuration of landmarks; (2) outline drawings of the species (blue) at a magnification of 2 X and the overall group-average outline drawings (azure); (3) thin-plate spline deformation grids reporting the shape variation from the overall group average (blue dots) and specimen variation (blue segments).
Figure 1 in Exploring species-level taxonomy in the Cryptocephalus flavipes species complex (Coleoptera: Chrysomelidae)
Figure 1. Collecting sites of specimens analysed. Abbreviations on map correspond to second element of symbols presented in Table 1.
Figure 3 from: Brunetti M, Magoga G, Iannella M, Biondi M, Montagna M (2019) Phylogeography and species distribution modelling of Cryptocephalus barii (Coleoptera: Chrysomelidae): is this alpine endemic species close to extinction? In: Schmitt M, Chaboo CS, Biondi M (Eds) Research on Chrysomelidae 8. ZooKeys 856: 3-25. https://doi.org/10.3897/zookeys.856.32462
Figure 3 Most likely migration model and altitudinal habitat maps reporting suitable area for the presence of the species during cold periods. A Most likely migration model. Arrows indicate unidirectional flows (in black) and bidirectional flows (in gray) between populations. B–F Suitable altitudinal habitat maps. In light grey are reported the areas suitable for the presence of the species above a certain altitudinal threshold; the yellow ellipses are schematic drawing of Cryptocephalusbarii populations; dendrograms showing the divergence events among populations, according to the tree in Fig. 1, are superimposed on the maps. At the bottom left of each map are reported: the minimum elevation at which climatic conditions are suitable for the presence of Cryptocephalusbarii (inferred from present knowledge) corresponding to the altitudinal threshold used to draw the suitable areas, and the corresponding estimates of temperature variation in respect to the present. Abbreviations: A.T. = altitudinal threshold; CON = Concarena; PRE = Presolana; ARE = Arera; ALB = Alben; GRI = Grigna; NGR = northern Grigna; SGR = southern Grigna; CG = Corna Grande; PEG = Pegherolo.
Figure 2 from: Brunetti M, Magoga G, Iannella M, Biondi M, Montagna M (2019) Phylogeography and species distribution modelling of Cryptocephalus barii (Coleoptera: Chrysomelidae): is this alpine endemic species close to extinction? In: Schmitt M, Chaboo CS, Biondi M (Eds) Research on Chrysomelidae 8. ZooKeys 856: 3-25. https://doi.org/10.3897/zookeys.856.32462
Figure 2 Maximum clade credibility tree and Minimum-spanning haplotype network. A Minimum-spanning haplotype network. Each colour represents a Cryptocephalusbarii population. Circles represent the different haplotypes; their diameter is proportional to the haplotypes abundance. B Maximum clade credibility tree. Horizontal blue bars represent 95% HPD age confidence intervals for the nodes. Under the main lineage nodes is reported the divergence time in thousands of years before present. Above the nodes Bayesian posterior probabilities > 0.8 are reported, black asterisks indicate Bayesian posterior probabilities values < 0.80. Vertical coloured bars on the right of the tree indicate monophyletic clades, the colours identify the C.barii populations. Under the tree, in blue, the estimated surface temperature for the last 800,000 years (Hansen et al. 2013).
Supplementary material 2 from: Brunetti M, Magoga G, Iannella M, Biondi M, Montagna M (2019) Phylogeography and species distribution modelling of Cryptocephalus barii (Coleoptera: Chrysomelidae): is this alpine endemic species close to extinction? In: Schmitt M, Chaboo CS, Biondi M (Eds) Research on Chrysomelidae 8. ZooKeys 856: 3-25. https://doi.org/10.3897/zookeys.856.32462
: Data type: statistical data
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