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Figure 1 Pelidnota burmeisteri burmeisteri Burmeister, 1844 in The taxonomic status of Pelidnota gounellei (Ohaus, 1908) and Pelidnota ludovici Ohaus, 1905 (Coleoptera: Scarabaeoidea: Melolonthidae)
Figure 1 Pelidnota burmeisteri burmeisteri Burmeister, 1844:A-C, male (dorsal, lateral, ventral); D-F, female (dorsal, lateral, ventral).
Figure 13 in The taxonomic status of Pelidnota gounellei (Ohaus, 1908) and Pelidnota ludovici Ohaus, 1905 (Coleoptera: Scarabaeoidea: Melolonthidae)
Figure 13 Pelidnota ebenina (Blanchard, 1842): A, male mesoventral process (dorsal); B, male posterior angle of metacoxa, metatrochanter and abdominal ventrite I in detail (dorsal); C, male metatibia (lateral); D, apex of metatibia in detail (lateral).
Figure 10 Pelidnota ludovici Ohaus, 1905 in The taxonomic status of Pelidnota gounellei (Ohaus, 1908) and Pelidnota ludovici Ohaus, 1905 (Coleoptera: Scarabaeoidea: Melolonthidae)
Figure 10 Pelidnota ludovici Ohaus, 1905:A, spiculum gastrale (dorsal);B-G, parameres; B, lateral carinae in detail (frontal);C-D, basal region of dorsal surface in detail;E, morphological variation of the parameres, inner margin divergent and free apex (frontal); F, aedeagus (lateral);G-I, lateral carinae and excavated aerea in lateral surface in detail.
Figure 9 Pelidnota ludovici Ohaus, 1905 in The taxonomic status of Pelidnota gounellei (Ohaus, 1908) and Pelidnota ludovici Ohaus, 1905 (Coleoptera: Scarabaeoidea: Melolonthidae)
Figure 9 Pelidnota ludovici Ohaus, 1905:A, male prosternal and mesoventral processes (dorsal); B, male posterior angle of metacoxa in detail (dorsal); C, male metatibia (lateral); D, apex of metatibia in detail (lateral); E, male abdominal ventrite VI (dorsal); F, male metarsomere V and outer metatarsal claw (lateral).
Figure 16 in The taxonomic status of Pelidnota gounellei (Ohaus, 1908) and Pelidnota ludovici Ohaus, 1905 (Coleoptera: Scarabaeoidea: Melolonthidae)
Figure 16 Pelidnota gounellei (Ohaus, 1908): A, male mesoventral process (dorsal); B, male posterior angle of metacoxa, metatrochanter and abdominal ventrite I in detail (dorsal); C, male metatibia (lateral); D, apex of metatibia in detail (lateral).
Figure 5 in The taxonomic status and geographic distribution of the European hare (Lepus europaeus Pallas, 1778) in Turkey (Mammalia: Lagomorpha)
Figure 5. The group centroids obtained from discriminant functions: 1 = Thracian specimen, 2 = Southwest Anatolian population, 3 = Central and East-Central Anatolian population, 4 = Northeast Anatolian population, 5 = Southeast Anatolian population.
Figure. Distribution of Neomys teres and Neomys anomalus species in Turkey (square = Neomys anomalus, triangle = Neomys teres). 1: Ulubey (Ordu), 2: Meryemana (Trabzon), 3: Kutul (Artvin), 4: Yalnızçam (Kars), 5: Bendimahi Canyon (Muradiye, Van), 6: Seyfe (Amasya), 7: Safranbolu (Karabük), 8: Topçam (Ordu), 9: Tamdere (Giresun), 10: Çamlık (Rize), 11: Ovid Mountain (Rize), 12: Lake Abant (Bolu), 13: Kayseri, 14: Erzurum, 15: Samsun, 16: Belgrad Forest (İstanbul), 17: Lake Abant (Bolu), 18: İrve creek (İstanbul), 19: Erçek Mountain (Van), 20: Paşaalandere (Tekirdağ), 21: Lake Terkos (İstanbul), 22: Yeşiloba (Adana), 23: Yenice, Çayır (Zonguldak), 24: Abant (Bolu), 25: Hanyatak village (Sakarya), 26: Longoz forest, Dupnisa cave, Demirköy (Kırklareli), 27: Lake Eber (Afyon), 28: Çırpılar (Çanakkale), 29: Uludağ (Bursa), 30: Balkusan (Karaman). in Taxonomic status of Neomys species (Mammalia: Soricomorpha) and their distribution in Turkey
Figure. Distribution of Neomys teres and Neomys anomalus species in Turkey (square = Neomys anomalus, triangle = Neomys teres). 1: Ulubey (Ordu), 2: Meryemana (Trabzon), 3: Kutul (Artvin), 4: Yalnızçam (Kars), 5: Bendimahi Canyon (Muradiye, Van), 6: Seyfe (Amasya), 7: Safranbolu (Karabük), 8: Topçam (Ordu), 9: Tamdere (Giresun), 10: Çamlık (Rize), 11: Ovid Mountain (Rize), 12: Lake Abant (Bolu), 13: Kayseri, 14: Erzurum, 15: Samsun, 16: Belgrad Forest (İstanbul), 17: Lake Abant (Bolu), 18: İrve creek (İstanbul), 19: Erçek Mountain (Van), 20: Paşaalandere (Tekirdağ), 21: Lake Terkos (İstanbul), 22: Yeşiloba (Adana), 23: Yenice, Çayır (Zonguldak), 24: Abant (Bolu), 25: Hanyatak village (Sakarya), 26: Longoz forest, Dupnisa cave, Demirköy (Kırklareli), 27: Lake Eber (Afyon), 28: Çırpılar (Çanakkale), 29: Uludağ (Bursa), 30: Balkusan (Karaman).
Figure 1 in Taxonomic status of a newly described island population of the smooth newt Lissotriton vulgaris (Linnaeus, 1758) from Bozcaada (Çanakkale, Turkey)
Figure 1. Geographic positions of the smooth newt populations used. Locality information is given in Table 1. Colors correspond to the various major clades (named after Babik et al., 2005; Pabijan et al., 2015). The three studied populations are given with a different symbol (star).
Figure 2 in Taxonomic status of a newly described island population of the smooth newt Lissotriton vulgaris (Linnaeus, 1758) from Bozcaada (Çanakkale, Turkey)
Figure 2. Phylogenetic relationships among studied smooth newt populations based on Bayesian Inference of mtDNA sequences (16S rRNA and ND4). Node posterior probabilities> 0.90 are given with asterisks. Population numbers correspond to Figure 1 and Table 1. The studied populations are given by their full names.
Figure 2 in Protected taxonomic status and lectotype designation for Holochila albosericea Miskin, 1891 (Lepidoptera: Lycaenidae)
Figure 2. Type material of Holochila caeruleolactea T.P. Lucas, 1891 showing dorsal and ventral views and labels: (A–C) lectotype male in SAMA (31-001721); (D–F) paralectotype female in SAMA (31-001722). Scale bars = 10 mm. Photo credits: 2A, C–F by Ben Parslow; 2B by Ted Edwards.
Figure 1 in Protected taxonomic status and lectotype designation for Holochila albosericea Miskin, 1891 (Lepidoptera: Lycaenidae)
Figure 1. Type material of Holochila albosericea Miskin, 1891 showing dorsal and ventral views and labels: (A–C) lectotype male in QM (T.12401); (D–F) paralectotype female in AMS (KL21390). Scale bars = 10 mm. Photo credits: 1A–C by Geoff Thompson; 1D–F by Natalie Tees.
Figure 4 in DNA barcoding and a new taxonomic status of the Triaenodes ochreellus lefkas Malicky, 1974 (Insecta, Trichoptera) with new distribution data
Figure 4. Distribution of Triaenodes ochreellus ochreellus (green field) and Triaenodes ochreellus lefkas (blue field) with new data in Albania, Croatia and Montenegro (red points).
Figure 3 in DNA barcoding and a new taxonomic status of the Triaenodes ochreellus lefkas Malicky, 1974 (Insecta, Trichoptera) with new distribution data
Figure 3. Maximum likelihood (Ml) phylogram based on the 658 bp long fragment of the DNA barcode region showing the relationships among the species of the genus Triaenodes. Numbers above the branches represent bootstrap support (bs) for Neighbor-Joining (NJ) and Ml analysis (NJ/Ml). BS values less than 70 are not shown. The groups delineated by Automatic Barcode Gap Discovery (ABGD) approach are shown on the right side of the tree.
Figure 1 in The taxonomic status of Argynnis pallescens Butler, 1873 stat. rev. from Japan and the Kuril Islands (Russia) (Lepidoptera: Nymphalidae)
Figure 1. Maximum likelihood phylogeny of Argynnis species (the subgenus Fabriciana) based on the COI barcode sequence dataset. Numbers near nodes are bootstrap support values. Scale bar on the tree indicates the branch lengths. Outgroup taxa (Melitaea cinxia, Araschnia levana, Issoria lathonia, Brenthis hecate, and Argynnis pandora) are not shown.
Figure 2. Argynnis pallescens Butler, 1873 in The taxonomic status of Argynnis pallescens Butler, 1873 stat. rev. from Japan and the Kuril Islands (Russia) (Lepidoptera: Nymphalidae)
Figure 2. Argynnis pallescens Butler, 1873 stat. rev. from Kunashir Island, Russia: A, C) Male; B, D) Female; E) Male genitalia; F) Habitat (meadow along birch forest with Kurile bamboo (Sasa kurilensis)).
FIGURE 10 in The taxonomic status of the genus Hubertoceras Spath: A new light on sexual dimorphism from the Callovian ammonites of Kutch, India
FIGURE 10. Parallel evolution of the species level for the genus Sivajiceras is plotted. Note that both M and m within the lineage show parallel evolutionary trends. Sources are: Waagen, 1875; Spath, 1931; Collignon, 1958; Callomon, 1993; Dutta and Bardhan, 2016.
FIGURE 11 in The taxonomic status of the genus Hubertoceras Spath: A new light on sexual dimorphism from the Callovian ammonites of Kutch, India
FIGURE 11. Parallel evolution of the species level for the genus Obtusicostites is plotted. Note that both M and m within the lineage show parallel evolutionary trends. Sources are: same as in Figure 10.
FIGURE 9 in The taxonomic status of the genus Hubertoceras Spath: A new light on sexual dimorphism from the Callovian ammonites of Kutch, India
FIGURE 9. Parallel evolution of median values of different morphological characters for three successive genera (including M and m) within Sivajiceratinae is plotted. Note that both M and m within the lineage show parallel evolutionary trends. D, U, W, and H are the same as in Figure 4. P= Primary rib (per half whorl) and S= Secondary rib (per half whorl). The dark horizontal line in the middle of the each box represents the median values, top frame of the box represents 75th percentile, bottom frame of the box represents 25th percentile and the bars at the end of vertical lines represent the minimum and the maximum data values without outliers (open circles). Sources are: Waagen, 1875; Spath, 1931; Collignon, 1958; Dutta and Bardhan, 2016.
FIGURE 8 in The taxonomic status of the genus Hubertoceras Spath: A new light on sexual dimorphism from the Callovian ammonites of Kutch, India
FIGURE 8. Transverse sections (body chamber hatched) of adult shells. 1. Obtusicostites obtusicosta (M). 2. Hubertoceras omphalodes (m). Note, for 1 and 2, overall similarity of whorl sections and depressed inner whorls with rounded umbilical edge. Septal sutural patterns. 3. Obtusicostites obtusicosta (M) at diameter 150 mm, redrawn from Waagen (1875, plate 38, figure 2). 4. Hubertoceras omphalodes (m) at diameter 48 mm, redrawn from Waagen (1875, plate 38, figure 4c). Scale bar equals 20 mm.
FIGURE 7 in The taxonomic status of the genus Hubertoceras Spath: A new light on sexual dimorphism from the Callovian ammonites of Kutch, India
FIGURE 7. Bivariate growth graphs between Hubertoceras omphalodes and macroconchs of the subfamily Sivajiceratinae. Maximum homogeneity of points is shown between Obtusicostites obtusicosta and Hubertoceras omphalodes. D=Diameter of the shell, U=Umbilical diameter, W=Width of the whorl and H=Height of the whorl. Measurements are taken at different ontogenetic stages of the specimens to accommodate intraspecific range of variability of each species. Photos are not to scale.
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