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835 results for “ground beetles”
Figure 5 from: Ashworth AC, Erwin TL (2016) Antarctotrechus balli sp. n. (Carabidae, Trechini): the first ground beetle from Antarctica. ZooKeys 635: 109-122. https://doi.org/10.3897/zookeys.635.10535
Figure 5 - Fossils of the left and right elytra of Antarctotrechus balli sp. n. A The left elytron, 2.36 mm in length, is designated as the paratype (USNM: ADP147732). A small part of the right elytron of the same individual is attached along the suture near the apex. The siltstone matrix is visible along the outer margin near the apex. The small rhomb-shaped crystals on the surface are authigenic calcite B The right elytron is designated as the holotype. (NMNH: ADP147741). The elytron is 2.40 mm in length. The base is deformed by a crack and concealed by sediment grains. A small part of the left elytron of the same individual is still attached along the suture near the base.
Figure 3 from: Ashworth AC, Erwin TL (2016) Antarctotrechus balli sp. n. (Carabidae, Trechini): the first ground beetle from Antarctica. ZooKeys 635: 109-122. https://doi.org/10.3897/zookeys.635.10535
Figure 3 - Ancient glacial deposits of the Meyer Desert Formation exposed in the Oliver Bluffs on the flanks of the Beardmore Glacier. The deposits are downthrown along the Koski fault which is marked by the prominent escarpment towards the north end of the bluffs (left on image). The type locality for Antarctotrechus balli sp. n. is at the north end of the bluffs marked by a red star.
Figure 2 from: Ashworth AC, Erwin TL (2016) Antarctotrechus balli sp. n. (Carabidae, Trechini): the first ground beetle from Antarctica. ZooKeys 635: 109-122. https://doi.org/10.3897/zookeys.635.10535
Figure 2 - An aerial view of the Oliver Bluffs on the Beardmore Glacier. Ice flow directions are shown by the blue arrows. The Meyer Desert Formation is downthrown to the north along the Koski Fault. The type locality for Antarctotrechus balli sp. n. is shown by a red star. The aerial image # TMA-2738-4 is from the collections of the The United States Antarctic Resource Center (USARC), USGS, Reston, VA.
Figure 4 from: Ashworth AC, Erwin TL (2016) Antarctotrechus balli sp. n. (Carabidae, Trechini): the first ground beetle from Antarctica. ZooKeys 635: 109-122. https://doi.org/10.3897/zookeys.635.10535
Figure 4 - The type locality for Antarctotrechus balli sp. n. is a siltstone lens within a sequence of lodgement tills exposed in the gulley wall to the left of the person highest in the gully.
Figure 1 from: Ashworth AC, Erwin TL (2016) Antarctotrechus balli sp. n. (Carabidae, Trechini): the first ground beetle from Antarctica. ZooKeys 635: 109-122. https://doi.org/10.3897/zookeys.635.10535
Figure 1 - The type locality for Antarctotrechus balli sp. n. is shown by the red star. Image map is a modified MODIS Mosaic of Antarctica from National Snow and Ice Data Center, http://nsidc.org/data/moa/
Figure 5 from: Fang J, Li W, Tian M (2016) Occurrence of cavernicolous ground beetles in Anhui Province, eastern China (Coleoptera, Carabidae, Trechinae). ZooKeys 625: 99-110. https://doi.org/10.3897/zookeys.625.9846
Figure 5 - Male genitalia of Wanoblemus wui Tian & Fang, gen. n., sp. n. a median lobe and parameres, lateral view b apical lobe, dorsal view.
Figure 2 from: Fang J, Li W, Tian M (2016) Occurrence of cavernicolous ground beetles in Anhui Province, eastern China (Coleoptera, Carabidae, Trechinae). ZooKeys 625: 99-110. https://doi.org/10.3897/zookeys.625.9846
Figure 2 - Male genitalia of Cimmeritodes (Zhecimmerites) parvus Tian & Li, sp. n., a median lobe and parameres, lateral view b apical lobe, dorsal view.
Figure 3 from: Fang J, Li W, Tian M (2016) Occurrence of cavernicolous ground beetles in Anhui Province, eastern China (Coleoptera, Carabidae, Trechinae). ZooKeys 625: 99-110. https://doi.org/10.3897/zookeys.625.9846
Figure 3 - Distribution map of cave-dwelling trechines in Anhui Province A map of China, arrowhead showing the cave biological study area; circle localities of Cimmeritodes (Zhecimmerites) parvus Tian & Li, sp. n., square localities of Wanoblemus wui Tian & Fang, gen. n., sp. n.
Figure 3 from: Raupach MJ, Hannig K, Morinière J, Hendrich L (2016) A DNA barcode library for ground beetles (Insecta, Coleoptera, Carabidae) of Germany: The genus Bembidion Latreille, 1802 and allied taxa. ZooKeys 592: 121-141. https://doi.org/10.3897/zookeys.592.8316
Figure 3 - Maximum statistical parsimony network of Bembidion species sharing COI haplotypes: A Bembidion atrocaeruleum Stephens, 1828 and Bembidion varicolor Fabricius, 1803 B Bembidion guttula (Fabricius, 1792) and Bembidion mannerheimii C.R. Sahlberg, 1827. Used settings included a user specified maximum of connection steps at 50, gaps were treated as fifth state. Each line represents a single mutational change whereas small black dots indicate missing haplotypes. The numbers of analyzed specimens (n) are listed, whereas the diameter of the circles is proportional to the number of haplotypes sampled (see given open half circles with numbers). Scale bars = 1 mm. Beetle images were obtained from www.eurocarabidae.de.
Figure 4 from: Raupach MJ, Hannig K, Morinière J, Hendrich L (2016) A DNA barcode library for ground beetles (Insecta, Coleoptera, Carabidae) of Germany: The genus Bembidion Latreille, 1802 and allied taxa. ZooKeys 592: 121-141. https://doi.org/10.3897/zookeys.592.8316
Figure 4 - Subtrees of the neighbor joining topology based on Kimura 2-parameter distances of all analyzed specimens of A Ocys harpaloides (Audinet-Serville, 1821) and nearest neighbor, and B Bembidion geniculatum Heer, 1837 and nearest neighbor. Branches with specimen ID-number from BOLD, species names and sample localities. Numbers next to internal nodes are non-parametric bootstrap values (in %).
FIGURES 1, 2 in Pterostichus neilgaimani sp. nov., a new species of ground beetles (Coleoptera: Carabidae) from relict sacred grove in Eastern Georgia
FIGURES 1, 2. Pterostichus neilgaimani sp. nov., male, holotype, 1—dorsal view, 2—ventral view.
Figures 4-9 from: Keller S, Hülsewig T (2018) Amended description and new combination for Entomophthora nebriae Raunkiaer, (1893), a little known entomopathogenic fungus attacking the ground beetle Nebria brevicollis (Fabricius, 1792). Alpine Entomology 2: 1-5. https://doi.org/10.3897/alpento.2.22136
Figures 4-9 4. Rhizoid with dark and sparsely branched ending together with resting spores (LPAO). 5. Cystidium with numerous nuclei (LPAO). 6. Dense layer of conidiophores with developing primary conidia (LPAO). 7. Primary conidia with prominent central vacuole (LPCB). 8. Young resting spores with nuclei (LPAO). 9. Mature resting spores with thick walls and one to several vacuoles depending on the stage of maturation (LPAO).
Figures 1-3 from: Keller S, Hülsewig T (2018) Amended description and new combination for Entomophthora nebriae Raunkiaer, (1893), a little known entomopathogenic fungus attacking the ground beetle Nebria brevicollis (Fabricius, 1792). Alpine Entomology 2: 1-5. https://doi.org/10.3897/alpento.2.22136
Figures 1-3 1. Nebria brevicollis at an early stage of fungus sporulation. At this stage the beetle is still able to move it's legs and antennae (nat. length of the beetle about 13 mm). 2. Beetle with fully sporulating fungus showing the extremely swollen abdomen. The strong cystidia are clearly visible at the edge of the fungus mass. 3. At the end of the sporulating period the mycelium turns yellowish (Photos: T. Hülsewig).
Fig. 2 in Sexual Size Dimorphism in Ground Beetle Carabus cumanus Fischer von Waldheim, 1823 (Coleoptera, Carabidae) and its Variation in Different Traits
Fig. 2. Descriptive statistics of morphometric traits in C. cumanus: a - elytra length, b - elytra width, c - pronotum length, d - pronotum width, e - head length, f - distance between eyes (Mean, Mean±2*SE, Mean±SD, - Outliers, * Extremes, f - females, m - males, 1 - steppe slope, 2 - flood plain forest)
Fig. 1 in Sexual Size Dimorphism in Ground Beetle Carabus cumanus Fischer von Waldheim, 1823 (Coleoptera, Carabidae) and its Variation in Different Traits
Fig. 1. Studied morphometric characteristics in C. cumanus (A – elytra length, B – elytra width, V – pronotum length, G – pronotum width, D – head length, E – distance between eyes)
Fig. 2 in Ancyrophora gracilis L , 1892 and Actinocephalus permagnus Wellmer, 1910 (Eugregarinorida: Apicomplexa) in natural populations of ground beetles (Coleoptera, Carabidae) - hosts preferences, intensity and seasonal dynamic
Fig. 2. Mean density of Actinocephalus permagnus (AT) and Ancyrophora gracilis (AC) in relation to habitat. Circle – woodland, square – meadow, triangle – arable land
Figures 10-19 from: Sasakawa K, Itô H (2018) Taxonomic notes on the ground beetles in the genus Trephionus Bates, 1883 from central Honshu, Japan (Coleoptera, Carabidae, Sphodrini, Synuchina). ZooKeys 742: 91-104. https://doi.org/10.3897/zookeys.742.23752
Figures 10-19 Left lateral (a) and dorsal (b) views of the endophallus and ventral view of the aedeagal apex (c) of Trephionus spp.: 10 T. kinoshitai from Mt. Shirouma 11 another specimen of T. kinoshitai from Mt. Shirouma, showing directions and examples of measurements for descriptions 12 T. cylindriphallus sp. n., holotype male; 13 T. cylindriphallus sp. n., a paratype male from Abe Pass 14 T. niumontanus sp. n., holotype male 15 T. babai from Mt. Ishikiri; 16 T. shibataianus from Mt. Naka 17 T. inexpectatus sp. n., holotype male 18 T. abiba sp. n., holotype male 19 T. bifidilobatus sp. n., holotype male. Abbreviations: AW, the width of the aedeagus at the ostium from the dorsal view; BD, the basal diameter of the lobe from dorsal view; da, dorsoapical lobe; db, dorsobasal lobe; go, gonopore; lb, left laterobasal lobe; rb, right laterobasal lobe; sl, sclerotized lobe.
Figures 2-9 from: Sasakawa K, Itô H (2018) Taxonomic notes on the ground beetles in the genus Trephionus Bates, 1883 from central Honshu, Japan (Coleoptera, Carabidae, Sphodrini, Synuchina). ZooKeys 742: 91-104. https://doi.org/10.3897/zookeys.742.23752
Figures 2-9 Dorsal view of Trephionus species: 2 T. kinoshitai, male from Mt. Shirouma 3 T. cylindriphallus sp. n., holotype male 4 T. niumontanus sp. n., holotype male 5 T. babai, male from Mt. Ishikiri 6 T. shibataianus, male from Mt. Naka 7 T. inexpectatus sp. n., holotype male 8 T. abiba sp. n., holotype male 9 T. bifidilobatus sp. n., holotype male.
Figure 1 from: Sasakawa K, Itô H (2018) Taxonomic notes on the ground beetles in the genus Trephionus Bates, 1883 from central Honshu, Japan (Coleoptera, Carabidae, Sphodrini, Synuchina). ZooKeys 742: 91-104. https://doi.org/10.3897/zookeys.742.23752
Figure 1 Distribution of Trephionus spp. in central Honshu based on specimens with unambiguous identities. ◆ T. nikkoensis ★ T. mikii ■ T. kinoshitai ▼ T. cylindriphallus sp. n. ▲ T. niumontanus sp. n. ● T. babai ○ T. subcavicola △ T. shibataianus ◇ T. inexpectatus sp. n. ☆ T. abiba sp. n. □ T. bifidilobatus sp. n. The type localities of T. nikkoensis, T. mikii, and T. subcavicola, which were not examined in this study, are shown, although the validities of their species statuses remain to be examined.
Figure 5 from: Raupach MJ, Hannig K, Morinière J, Hendrich L (2018) A DNA barcode library for ground beetles of Germany: the genus Amara Bonelli, 1810 (Insecta, Coleoptera, Carabidae). ZooKeys 759: 57-80. https://doi.org/10.3897/zookeys.759.24129
Figure 5 - Maximum statistical parsimony network of Amara alpina (Paykull, 1790) and Amara torrida Panzer, 1796. Used parameters included default settings for connection steps whereas gaps were treated as fifth state. Each line represents a single mutational change whereas small black lines indicate missing haplotypes. The numbers of analysed specimens (n) are listed, the diameter of the circles is proportional to the number of haplotypes sampled (see given open half circles with numbers). Scale bars 1 mm. Beetle images were obtained from www.eurocarabidae.de.
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