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Figure 5 from: Kaneko N, Wada K (2020) Catalogue of the type material of Scarabaeoidea (Coleoptera) deposited in the Research Institute of Evolutionary Biology, Tokyo, Japan. ZooKeys 958: 35-89. https://doi.org/10.3897/zookeys.958.52799
Figure 5 Habitus of holotype specimens. ATibiotrichius vietnamensis Miyake BCharitovalgus banzai Sawada CDasyvalgus annamensis Miyake DDasyvalgus castaneodorsalis Miyake EDasyvalgus decamaculatus Miyake FDasyvalgus flavicauda Miyake GDasyvalgus macacus Miyake HDasyvalgus multicus Miyake.
Figure 1 from: Kaneko N, Wada K (2020) Catalogue of the type material of Scarabaeoidea (Coleoptera) deposited in the Research Institute of Evolutionary Biology, Tokyo, Japan. ZooKeys 958: 35-89. https://doi.org/10.3897/zookeys.958.52799
Figure 1 Habitus of holotype specimens. ARhyparus kitanoi (Miyake) BAdoretus (Lepadoretus) ubonensis (Miyake, Yamaguchi et Aoki) CAnomala flavoguttata Miyake DAnomala ohmomoi Miyake, Yamaguchi et Aoki EAnomala thailandiana Miyake, Yamaguchi et Akiyama FCallistethus isidai Miyake GMalaia castanoptera Miyake HMalaia macassara Miyake.
Figure 9 from: Spiridonov VA, Simakova UV, Anosov SE, Zalota AK, Timofeev VA (2020) Review of Macropodia in the Black Sea supported by molecular barcoding data; with the redescription of the type material, observations on ecology and epibiosis of Macropodia czernjawskii (Brandt, 1880) and notes on other Atlanto-Mediterranean species of Macropodia Leach, 1814 (Crustacea, Decapoda, Inachidae). Zoosystematics and Evolution 96(2): 609-635. https://doi.org/10.3897/zse.96.48342
Figure 9 Morphometric relationships and fecundity characteristics of Macropodia czernjawskii. a. Relationships between carapace width (CW) and the geometric mean of chela length, height and thickness (ChGM). b. Relationships between CW and decimal logarithm of the number of developing eggs (I or II stage of development) on pleopods (F). For statistical data see Table 2.
Figure 7 from: Spiridonov VA, Simakova UV, Anosov SE, Zalota AK, Timofeev VA (2020) Review of Macropodia in the Black Sea supported by molecular barcoding data; with the redescription of the type material, observations on ecology and epibiosis of Macropodia czernjawskii (Brandt, 1880) and notes on other Atlanto-Mediterranean species of Macropodia Leach, 1814 (Crustacea, Decapoda, Inachidae). Zoosystematics and Evolution 96(2): 609-635. https://doi.org/10.3897/zse.96.48342
Figure 7 Macropodia czernjawskii. a. Right chela, male, CW 11.0 (ZMMU Ma 3547); b. Right chela, male. CW 6.0 mm (ZMMU Ma 3544) c. Malformed right chela, male, CW 8.0 mm (ZMMU Ma 3543); d, e. Same specimen as c. dactylus and propodus of P 5. Scale bars: 1 mm (a–c, e), 0.5 mm (d).
Figure 6 from: Spiridonov VA, Simakova UV, Anosov SE, Zalota AK, Timofeev VA (2020) Review of Macropodia in the Black Sea supported by molecular barcoding data; with the redescription of the type material, observations on ecology and epibiosis of Macropodia czernjawskii (Brandt, 1880) and notes on other Atlanto-Mediterranean species of Macropodia Leach, 1814 (Crustacea, Decapoda, Inachidae). Zoosystematics and Evolution 96(2): 609-635. https://doi.org/10.3897/zse.96.48342
Figure 6 Macropodia czernjawskii. a. Anterior part of the body with basal antennal segment (ZMMU Ma 3543); b. Anterior part of the body with basal antennal segments, male (ZMMU Ma 3547). c. Male pleon (ZMMU Ma 3547); d. Female sterno-pleonal cavity with exposed genital segment (ZMMU Ma 3538). Scale bar: 1 mm.
Figure 5 from: Spiridonov VA, Simakova UV, Anosov SE, Zalota AK, Timofeev VA (2020) Review of Macropodia in the Black Sea supported by molecular barcoding data; with the redescription of the type material, observations on ecology and epibiosis of Macropodia czernjawskii (Brandt, 1880) and notes on other Atlanto-Mediterranean species of Macropodia Leach, 1814 (Crustacea, Decapoda, Inachidae). Zoosystematics and Evolution 96(2): 609-635. https://doi.org/10.3897/zse.96.48342
Figure 5 Macropodia czernjawskii, photographs in natural coloration. a. male (ZMMU Ma 3547), dorsal view. b. Same specimen as a. ventral view. c. female ov (ZMMU Ma 3542), dorsal view. d. Same specimen as c. ventral view. Scale bar: 10 mm. Photographs by SE Anosov.
Figure 4 from: Spiridonov VA, Simakova UV, Anosov SE, Zalota AK, Timofeev VA (2020) Review of Macropodia in the Black Sea supported by molecular barcoding data; with the redescription of the type material, observations on ecology and epibiosis of Macropodia czernjawskii (Brandt, 1880) and notes on other Atlanto-Mediterranean species of Macropodia Leach, 1814 (Crustacea, Decapoda, Inachidae). Zoosystematics and Evolution 96(2): 609-635. https://doi.org/10.3897/zse.96.48342
Figure 4 Macropodia czernjawskii (a, b. possible paralectotype ZIN-RAS 1609; c, d.ZIN-RAS 35102) and Macropodia longirostris (JC Fabricius, 1775) (e.SMF 3752). a. Right cheliped, ventral view. b. Right cheliped, dorsal view. c. Cphalothorax, dorsal view. d. Cephalothorax, ventral view. e. Cephalothorax, dorsal view. Scale bar: 10 mm.
Figure 3 from: Spiridonov VA, Simakova UV, Anosov SE, Zalota AK, Timofeev VA (2020) Review of Macropodia in the Black Sea supported by molecular barcoding data; with the redescription of the type material, observations on ecology and epibiosis of Macropodia czernjawskii (Brandt, 1880) and notes on other Atlanto-Mediterranean species of Macropodia Leach, 1814 (Crustacea, Decapoda, Inachidae). Zoosystematics and Evolution 96(2): 609-635. https://doi.org/10.3897/zse.96.48342
Figure 3 Comparison of Macropodia czernjawskii (a–d. possible paralectotype, male, ZIN-RAS 88750) to Macropodia tenuirostris (Leach, 1814) (a'–d'. male, SMF 3749) and Macropodia rostrata (Linnaeus, 1761) (a''–d''.SMF 40660). a. Dorsal view. b. Lateral view. c. Anterior part of the body, with antennules, basal antennal segments, and epistome, ventral view. d. Dactylus of pereopod 5. Scale bars: 10 mm (a–a''–b–b''), 1 mm (c–c''–d–d'').
Figure 2 from: Spiridonov VA, Simakova UV, Anosov SE, Zalota AK, Timofeev VA (2020) Review of Macropodia in the Black Sea supported by molecular barcoding data; with the redescription of the type material, observations on ecology and epibiosis of Macropodia czernjawskii (Brandt, 1880) and notes on other Atlanto-Mediterranean species of Macropodia Leach, 1814 (Crustacea, Decapoda, Inachidae). Zoosystematics and Evolution 96(2): 609-635. https://doi.org/10.3897/zse.96.48342
Figure 2 Macropodia czernjawskii (Brandt, 1880), female lectotype (ZIN-RAS 88751). a. Dorsal view. b. Ventral view. c. Lateral view. Scale bar: 5 mm.
Figure 8 from: Spiridonov VA, Simakova UV, Anosov SE, Zalota AK, Timofeev VA (2020) Review of Macropodia in the Black Sea supported by molecular barcoding data; with the redescription of the type material, observations on ecology and epibiosis of Macropodia czernjawskii (Brandt, 1880) and notes on other Atlanto-Mediterranean species of Macropodia Leach, 1814 (Crustacea, Decapoda, Inachidae). Zoosystematics and Evolution 96(2): 609-635. https://doi.org/10.3897/zse.96.48342
Figure 8 Macropodia czernjawskii. Male (ZMMU Ma 3543), right gonopod . a. Pleonal view. b. Sternal view. Scale bar: 1 mm.
Figure 12 from: Spiridonov VA, Simakova UV, Anosov SE, Zalota AK, Timofeev VA (2020) Review of Macropodia in the Black Sea supported by molecular barcoding data; with the redescription of the type material, observations on ecology and epibiosis of Macropodia czernjawskii (Brandt, 1880) and notes on other Atlanto-Mediterranean species of Macropodia Leach, 1814 (Crustacea, Decapoda, Inachidae). Zoosystematics and Evolution 96(2): 609-635. https://doi.org/10.3897/zse.96.48342
Figure 12 Phylogenetic relationships of Macropodia spp. based on partial sequence of the COI gene, obtained using Bayesian inference. Tips of the tree colored according to their morphological identification. Numbers above the branches are the posterior probabilities.
Figure 10 from: Spiridonov VA, Simakova UV, Anosov SE, Zalota AK, Timofeev VA (2020) Review of Macropodia in the Black Sea supported by molecular barcoding data; with the redescription of the type material, observations on ecology and epibiosis of Macropodia czernjawskii (Brandt, 1880) and notes on other Atlanto-Mediterranean species of Macropodia Leach, 1814 (Crustacea, Decapoda, Inachidae). Zoosystematics and Evolution 96(2): 609-635. https://doi.org/10.3897/zse.96.48342
Figure 10 Natural habitats of Macropodiz czernjawskii in the Black Sea. a, b. Male (ZMMU Ma 3549) in Cystoseira sp., on rock, Tuaphat coastal rock masif, near Gelendzhik. c. Male (ZMMU Ma 3547), on sand, of Blagoveschenskaya village, near Anapa. d. Specimen collected of Blagoveschensakya in aquarium, decorated with red algae after few days of keeping. e. A characteristic biotope of M. czernjawskii in Tuaphat. f. Biotope in Kazachya Cove, Crimean Peninsula where M. czernjawskii has been repeatedly observed. Photographs by SE Anosov.
Figure 1 from: Spiridonov VA, Simakova UV, Anosov SE, Zalota AK, Timofeev VA (2020) Review of Macropodia in the Black Sea supported by molecular barcoding data; with the redescription of the type material, observations on ecology and epibiosis of Macropodia czernjawskii (Brandt, 1880) and notes on other Atlanto-Mediterranean species of Macropodia Leach, 1814 (Crustacea, Decapoda, Inachidae). Zoosystematics and Evolution 96(2): 609-635. https://doi.org/10.3897/zse.96.48342
Figure 1 Study area and the original records of Macropodia czernjawskii in the Black Sea presented in this study.
Figure 11 from: Spiridonov VA, Simakova UV, Anosov SE, Zalota AK, Timofeev VA (2020) Review of Macropodia in the Black Sea supported by molecular barcoding data; with the redescription of the type material, observations on ecology and epibiosis of Macropodia czernjawskii (Brandt, 1880) and notes on other Atlanto-Mediterranean species of Macropodia Leach, 1814 (Crustacea, Decapoda, Inachidae). Zoosystematics and Evolution 96(2): 609-635. https://doi.org/10.3897/zse.96.48342
Figure 11 Estimates of evolutionary divergence over sequence pairs within and between species of Macropodia (M. czernjawskii; M. rostrata – M. parva; M. tenuirostris – M. longipes; the latter two pairs and M. parva, M. rostrata – Macropodia sp. are indicated as "?", meaning their possible conspecificity); and between genera of Majoidea. The number of base substitutions per site from averaging over all sequence pairs between groups are shown. Analyses were conducted using the Kimura 2-parameter mode. For values of K2P see also Table 3.
Supplementary material 1 from: Spiridonov VA, Simakova UV, Anosov SE, Zalota AK, Timofeev VA (2020) Review of Macropodia in the Black Sea supported by molecular barcoding data; with the redescription of the type material, observations on ecology and epibiosis of Macropodia czernjawskii (Brandt, 1880) and notes on other Atlanto-Mediterranean species of Macropodia Leach, 1814 (Crustacea, Decapoda, Inachidae). Zoosystematics and Evolution 96(2): 609-635. https://doi.org/10.3897/zse.96.48342
Table S1
FIGURE 1 in Redescription of Filchneria mongolica (Klapálek, 1901) (Plecoptera, Perlodidae) based on type eggs and fresh material from the Selenga and Amur River Basins of Russia and Mongolia
FIGURE 1. Filchneria mongolica, female, habitus (Photograph by M.P. Tiunov).
FIGURE 1 in Clarification of type material for Bornean species of the genus Osteochilus (Cyprinidae)
FIGURE 1. Holotype of Osteochilus ingeri; FMNH 68540, 111.8mm SL.
FIGURE 2 in Clarification of type material for Bornean species of the genus Osteochilus (Cyprinidae)
FIGURE 2. Holotype of Osteochilus sarawakensis; FMNH 94182, 138.5mm SL.
FIGURE 3 in Clarification of type material for Bornean species of the genus Osteochilus (Cyprinidae)
FIGURE 3. Holotype of Osteochilus kahajanensis chini; FMNH 68230, 127.8mm SL.
FIGURE 65 in A redescription of Metopa species (Amphipoda, Stenothoidae) based on the type material. 3. Natural History Museum, Oslo (NHM) 2465
FIGURE 65. Distribution map of E: Metopa borealis Sars, 1883 and F: Metopa invalida Sars, 1892
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Allen Brain Atlas
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International Brain Laboratory public data
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OpenNeuro
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