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28 results for “blister beetles”
Figure 1 in Record of the blister beetle, Croscherichia goryi (Marseul, 1870) (Coleoptera: Meloidae) from Rajasthan, India
Figure 1. Croscherichia goryi (Marseul, 1870) male 1-8: 1. Elytral pattern, 2. Mesosternum, 3. Antennae, 4. Claws, 5. Pronotum, 6. Last abdominal sternite, 7. Male genitalia (Tegmen a. ventral and b. lateral view), 8. Aedeagus, lateral view, 9. Spiculum gastrale. Sacle bar 1 mm.
Plate I in Record of the blister beetle, Croscherichia goryi (Marseul, 1870) (Coleoptera: Meloidae) from Rajasthan, India
Plate I. Croscherichia goryi (Marseul, 1870) male 1-10: 1. Habitus, 2. Mesosternum without a 'Scutum', 3. Antennae (3rd antennal segment subequal in length to 1st segment, Antennae progressively widened from segments VI to apex), 4. Hind tibial spurs dissimilar, 5. Claws, 6. Pronotum, 7. Last abdominal sternite, 8. Male genitalia (Tegmen a. Dorsal, b. Ventral and c. Lateral view), 9. Aedeagus, lateral view, 10. Spiculum gastrale.
Data from: Latitudinal variation and coevolutionary diversification of sexually dimorphic traits in the false blister beetle Oedemera sexualis
Sexual traits are subject to evolutionary forces that maximize reproductive benefits and minimize survival costs, both of which can depend on environmental conditions. Latitude explains substantial variation in environmental conditions. However, little is known about the relationship between sexual trait variation and latitude, although body size often correlates with latitude. We examined latitudinal variation in male and female sexual traits in 22 populations of the false blister beetle Oedemera sexualis in the Japanese Archipelago. Males possess massive hind legs that function as a female‐grasping apparatus, while females possess slender hind legs that are used to dislodge mounting males. Morphometric analyses revealed that male and female body size (elytron length), length and width of the hind femur and tibia, and allometric slopes of these four hind leg dimensions differed significantly among populations. Of these, three traits showed latitudinal variation, namely, male hind femur was stouter; female hind tibia was slenderer, and female body was smaller at lower latitudes than at higher latitudes. Hind leg sizes and shapes, as measured by principal component analysis of these four hind leg dimensions in each sex, covaried significantly between sexes, suggesting coevolutionary diversification in sexual traits. Covariation between sexes was weaker when variation in these traits with latitude was removed. These results suggest that coevolutionary diversification between male and female sexual traits is mediated by environmental conditions that vary with latitude.
FIGURE 31 in Revision of the nearctic blister beetle genus Tricrania LeConte, 1860 (Coleoptera: Meloidae: Nemognathinae)
FIGURE 31. Phenological occurrence of (A.) T. sanguinipennis, and (B) T. stansburii. Data derived from information in appendices 2 and 3, as well as pers. obs. of authors.
FIGURE 30 in Revision of the nearctic blister beetle genus Tricrania LeConte, 1860 (Coleoptera: Meloidae: Nemognathinae)
FIGURE 30. Distribution of T. sanguinipennis (triangle "˔") and T. stansburii (circle "●"). Question marks ("?") indicate state records for T. sanguinipennis that did not have specific locality data, or records that could not be substantiated.
FIGURES 22–29 in Revision of the nearctic blister beetle genus Tricrania LeConte, 1860 (Coleoptera: Meloidae: Nemognathinae)
FIGURES 22–29. First instar larvae: habitus, lateral view (22) T. sanguinipennis, (23) T. stansburii; habitus, ventral view (24) T. sanguinipennis (25) T. stansburii; head, ventral view (26) T. sanguinipennis (27) T. stansburii; metathoracic leg, ventral view (28) T. sanguinipennis (29) T. stansburii.
FIGURES 14–21 in Revision of the nearctic blister beetle genus Tricrania LeConte, 1860 (Coleoptera: Meloidae: Nemognathinae)
FIGURES 14–21. Mouthparts: labrum, dorsal view (14) T. sanguinipennis (15) T. stansburii; mandibles, dorsal view (16) T. sanguinipennis (17) T. stansburii; right maxilla, ventral view (18) T. sanguinipennis (19) T. stansburii; labium, ventral view (20) T. sanguinipennis (21) T. stansburii.
FIGURES 8–13 in Revision of the nearctic blister beetle genus Tricrania LeConte, 1860 (Coleoptera: Meloidae: Nemognathinae)
FIGURES 8–13. Male genitalia: tegmen, lateral view (8) T. sanguinipennis (11) T. stansburii; tegmen, ventral view (9) T. sanguinipennis (12) T. stansburii; median lobe of aedeagus, lateral view (10) T. sanguinipennis (13) T. stansburii.
Fig. 3 in Endemic and cryptic: different biogeographic histories of three Italian blister beetles of the genus Meloe (Coleoptera: Meloidae: Meloinae: Meloini)
Fig. 3. Maximum likelihood tkee based on COI sequences of analyzed specimens of Meloe %Eurymeloe). Only suppokted values of nodes %UFBootstkap, UFB ≥ 95 and SH-aLRT ≥ 80%) ake kepokted %SH-LRT/UFB).;ashes %–) indicate non-suppokted values. Coloked vektical baks on the kight shown species delimitation analysis kesults %ASAP, ad hoc, and mPTP) %https://inkscape.okg/it/).
Fig. 8 in Endemic and cryptic: different biogeographic histories of three Italian blister beetles of the genus Meloe (Coleoptera: Meloidae: Meloinae: Meloini)
Fig. 8. Thkee diffekent pattekns of biogeogkaphic discunction and theik kelative moleculak dating %with the 95%HP; in squake bkackets) obsekved in %A) M. orobates and M. digiuliorum; %B) M. apenninicus and M. rugosus ′ M. cfk. rugosus; and %C) M. b. baudii and M. b. glazunovi %https://inkscape.okg/it/).
Fig. 6 in Endemic and cryptic: different biogeographic histories of three Italian blister beetles of the genus Meloe (Coleoptera: Meloidae: Meloinae: Meloini)
Fig. 6. Male habitus, doksal view, of %A) M. b. baudii, %B) M. b. glazunovi, and %C) M. scabriusculus. Scale bak 1 mm %https://inkscape.okg/it/).
Fig. 2 in Endemic and cryptic: different biogeographic histories of three Italian blister beetles of the genus Meloe (Coleoptera: Meloidae: Meloinae: Meloini)
Fig. 2. Multilocus %16S, COI, CA;, and 28S) phylogenetic tkee of Meloe %Eurymeloe). Topology cokkesponds to the maximum likelihood %ML) tkee. Clades ake indicated with letteks %a–t). Only suppokted values of nodes %UFBootstkap, UFB ≥ 95 ands SH-aLRT ≥ 80%; postekiok pkobability, PP ≥ 0.95) ake kepokted %SH-LRT/ UFB/PP).;ashes %–) indicate non-suppokted values. Clades of species that weke not the main focus of the study ake collapsed. Fok a non-collapsed veksion of the tkee, see Supplementaky Fig. S4 %https://inkscape.okg/it/).
Fig. 7 in Endemic and cryptic: different biogeographic histories of three Italian blister beetles of the genus Meloe (Coleoptera: Meloidae: Meloinae: Meloini)
Fig. 7.;oksal and latekal views of male genitalia: %A–C) M. b. baudii, %;–F) M. b. glazunovi, and %G–I) M. scabriusculus. Scale bak 0.5 mm %https://inkscape.okg/it/).
Fig. 5 in Endemic and cryptic: different biogeographic histories of three Italian blister beetles of the genus Meloe (Coleoptera: Meloidae: Meloinae: Meloini)
Fig. 5.;oksal and latekal views of male genitalia: %A–C) M. orobates %fkom: Sánchez-Vialas et al. 2022), %;–F) M. digiuliorum sp. n., %G–I) M. apenninicus, %J–L) M. rugosus. Scale bak 0.5 mm %https://inkscape.okg/it/).
Fig. 1 in Endemic and cryptic: different biogeographic histories of three Italian blister beetles of the genus Meloe (Coleoptera: Meloidae: Meloinae: Meloini)
Fig. 1. Italian endemic taxa of Meloe (Eurymeloe) %uppek kow) and theik type localities %lowek kow): %A) M. digiuliorium sp. nov.; %B) M. apenninicus; %C) M. b. baudii; %;) Abkuzzo, L'Aquila pkov., Ovindoli, Fkeddo Mt. westekn slope; %E) Sicily, Messina pkov., Cesakò, nk. Poktella di femmina mokta; %F) Abkuzzo, L'Aquila pkov., Cekchio, basal westekn slope of the Sikente Mt. Photo's ckedits: A, L. Spagoni; B–E, A. Ricceki; F, M.A. Bologna %https://inkscape.okg/it/).
Fig. 4 in Endemic and cryptic: different biogeographic histories of three Italian blister beetles of the genus Meloe (Coleoptera: Meloidae: Meloinae: Meloini)
Fig. 4. Male habitus, doksal view, of %A) M. orobates %fkom: Sánchez-Vialas et al. 2022), %B) M. digiuliorum sp. n., %C) M. apenninicus, %;) M. rugosus. Scale bak 1 mm %https://inkscape.okg/it/).
FIGURE 4 in The false-blister beetles (Coleoptera, Oedemeridae) of Oman with the description of a new species
FIGURE 4. Example of habitats for Oedemeridae in Oman. 4a: Wahiba sandy dunes (Alloxantha talhouki); 4b: Al Rajmi (Nacerdochroa carinatopyga, Alloxantha flava); 4c: Shinas (Probosca (Proboxantha) fuscipennis); 4d: Wadi Damm (N. carinatopyga, A. flava).
FIGURE 3 in The false-blister beetles (Coleoptera, Oedemeridae) of Oman with the description of a new species
FIGURE 3. Known distribution of Probosca (Proboxantha) coniuncta n. sp. Maps from Google satellite (left map, https:// google-satellite.gosur.com, last access 10/5/2022) and ESRI (www.arcgis.com, last access 10/5/2022).
FIGURE 1 in The false-blister beetles (Coleoptera, Oedemeridae) of Oman with the description of a new species
FIGURE 1. Probosca (Proboxantha) coniuncta n. sp., holotype male (a), paratype female (b), paratype male, variability (c).
Data from: Genetic population structure of the blister beetle Gnathium minimum: core and peripheral populations
Populations on the periphery of a species' range tend to contain lower genetic variation and increased genetic differentiation compared to populations at the core of a species range, although some exceptions to this generalization occur. The blister beetle Gnathium minimum (Say) exhibits a wide-ranging distribution in the western United States but has peripheral or disjunct populations in Mexico, Florida, and Wisconsin. We used amplified fragment length polymorphism (AFLP) to compare the genetic variation and magnitude of genetic differentiation of the Wisconsin peripheral population to western core populations (Colorado, Kansas, New Mexico, and Texas). The proportion of polymorphic loci was 53.6 and 54.3, and expected heterozygosity 0.1864 and 0.1933 for the Kansas/Colorado (n = 87) and New Mexico/Texas (n = 35) regions, respectively. Specimens from Wisconsin (n = 121) had a lower proportion of polymorphic loci (38.4) and expected heterozygosity (0.1475). Genetic cluster estimation with GENELAND and F ST values showed greater genetic differentiation among the sampling locations within Wisconsin compared to core regions. Significant isolation-by-distance (IBD) was also observed in Wisconsin but not within the core regions. Lower genetic variation and increased isolation may reduce the Wisconsin population's ability to respond to change, thereby increasing their susceptibility to extinction.
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