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Fig. 4 in A new Beneziphius beaked whale from the ocean floor off Galicia, Spain and biostratigraphic reassessment of the type species

Fig. 4. Vertex of the partial cranium of a beaked whale Beneziphius cetariensis sp. nov., holotype (SGHNMF MA0953) from the middle Miocene to early Pliocene of A Selva fishing ground, off the Galician coast, Spain, in dorsal view. Interpretive drawing (A) and photograph (B).

Fig. 3 in A new Beneziphius beaked whale from the ocean floor off Galicia, Spain and biostratigraphic reassessment of the type species

Fig. 3. Partial cranium of a beaked whale Beneziphius cetariensis sp. nov., holotype (SGHNMF MA0953) from the middle Miocene to early Pliocene of A Selva fishing ground, off the Galician coast, Spain, in anterior and slightly dorsal view.

Fig. 7 in A new Beneziphius beaked whale from the ocean floor off Galicia, Spain and biostratigraphic reassessment of the type species

Fig. 7. Simplified palaeogeographic map of NW Europe, showing coastlines and the limits of the continental shelf (light grey) during the Serravallian– Tortonian (late middle to early late Miocene). Black star is the type locality of Beneziphius cetariensis sp. nov. (A Selva fishing ground) and white star is the type locality of B. brevirostris (Antwerp, Belgium). Other fossil ziphiid species are listed whose corresponding genera are found in at least two regions. Map redrawn from Scotese (2014). Note that the North Atlantic–Mediterranean connection was probably more complex than illustrated in this schematic map (e.g., Kouwenhoven and van der Zwaan 2006).

Fig. 5 in A new Beneziphius beaked whale from the ocean floor off Galicia, Spain and biostratigraphic reassessment of the type species

Fig. 5. Detail of the results of the phylogenetic analyses of the family Ziphiidae for the "Messapicetus clade". A. Strict consensus of the heuristic search with equally-weighted characters, showing the unresolved relationships of Beneziphius cetariensis sp. nov. and B. brevirostris. B. Single most parsimonious tree of the heuristic search with downweighted homoplastic characters (k = 3), with B. cetariensis sp. nov. more stemward than B. brevirostris. Results for the other parts of the clade Ziphiidae follow Bianucci et al. (2016).

Fig. 1 in A new Beneziphius beaked whale from the ocean floor off Galicia, Spain and biostratigraphic reassessment of the type species

Fig. 1. Partial cranium of a beaked whale Beneziphius cetariensis sp. nov., holotype (SGHNMF MA0953) from the middle Miocene to early Pliocene of A Selva fishing ground, off the Galician coast, Spain, in dorsal (A) and left lateral (B) views. Interpretive drawings (A1, B1) and photographs (A2, B2).

Fig. 2 in A new Beneziphius beaked whale from the ocean floor off Galicia, Spain and biostratigraphic reassessment of the type species

Fig. 2. Partial cranium of a beaked whale Beneziphius cetariensis sp. nov., holotype (SGHNMF MA0953) from the middle Miocene to early Pliocene of A Selva fishing ground, off the Galician coast, Spain, in right lateral (A) and ventral (B) views.

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Рис. 5. Типовое местонахожΑение Dorcadion natali sp. n. Fig. 5. The type locality of Dorcadion natali sp. n. in A new species of Dorcadion Dalman, 1817 (Coleoptera: Cerambycidae) from East Kazakhstan

Рис. 5. Типовое местонахожΑение Dorcadion natali sp. n. Fig. 5. The type locality of Dorcadion natali sp. n.

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Рис. 1. Распространение виΑов Dorcadion (s. str.) Dalman, 1817 в Восточном Казахстане. 1 – южные преΑгорья хр. Тарбагатай, типовое местонахожΑение D. urdzharicum; 2 – северные преΑгорья и скΛоны Тарбагатая и Саура, местонахожΑение D. songaricum; 3 – степи северо-запаΑнее оз. СасыккоΛь, местонахожΑение D. cephalotes; 4 – преΑгорья у югозапаΑного берега оз. АΛакоΛь, типовое местонахожΑение D. alakoliense; 5 – 47 км юго-восточнее Маканчи, типовое местонахожΑение D. natali sp. n. Fig. 1. Localities of species of Dorcadion (s. str.) Dalman, 1817 in East Kazakhstan. 1 – southern foothills of the Tarbagatai Ridge, type locality of D. urdzharicum; 2 – northern foothills and slopes of the Tarbagatai and Saur, locality of D. songaricum; 3 – steppes NW of Sasykkol Lake, locality of D. cephalotes; 4 – foothills at the SW shore of Alakol Lake, type locality of D. alakoliense; 5 – 47 km SE Makanchi, type locality of D. natali sp. n. in A new species of Dorcadion Dalman, 1817 (Coleoptera: Cerambycidae) from East Kazakhstan

Рис. 1. Распространение виΑов Dorcadion (s. str.) Dalman, 1817 в Восточном Казахстане. 1 – южные преΑгорья хр. Тарбагатай, типовое местонахожΑение D. urdzharicum; 2 – северные преΑгорья и скΛоны Тарбагатая и Саура, местонахожΑение D. songaricum; 3 – степи северо-запаΑнее оз. СасыккоΛь, местонахожΑение D. cephalotes; 4 – преΑгорья у югозапаΑного берега оз. АΛакоΛь, типовое местонахожΑение D. alakoliense; 5 – 47 км юго-восточнее Маканчи, типовое местонахожΑение D. natali sp. n. Fig. 1. Localities of species of Dorcadion (s. str.) Dalman, 1817 in East Kazakhstan. 1 – southern foothills of the Tarbagatai Ridge, type locality of D. urdzharicum; 2 – northern foothills and slopes of the Tarbagatai and Saur, locality of D. songaricum; 3 – steppes NW of Sasykkol Lake, locality of D. cephalotes; 4 – foothills at the SW shore of Alakol Lake, type locality of D. alakoliense; 5 – 47 km SE Makanchi, type locality of D. natali sp. n.

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FIGURE 2. Dromilites belli n in Revision of Dromilites bucklandii (Crustacea, Decapoda, Brachyura): Type material revealing its real identity, a junior synonym, and a new species

FIGURE 2. Dromilites belli n. sp. type series from the Ypresian of London Clay (Copenhagen Fields, London, United Kingdom). 1. Holotype NHMUK PI OR 59089 (Wetherell coll.) coated with ammonium chloride (female individual): 1a. carapace in dorsal view, 1b. carapace in frontal view, 1c. carapace in ventral view, 1d. carapace in left-lateral view; 2. Paratype NHMUK PI OR 59091 (Wetherell coll.) coated with ammonium chloride (male individual): 2a. carapace in dorsal view, 2b. carapace in frontal view, 2c. carapace in ventral view, 2d. carapace in left-lateral view. Scale bars equal 10 mm. Photographs: Philip Hurst, Natural History Museum, London.

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FIGURE 1. Dromilites bucklandii H. Milne Edwards, 1937. 1. Lectotype MNHN.F.B21561 in Revision of Dromilites bucklandii (Crustacea, Decapoda, Brachyura): Type material revealing its real identity, a junior synonym, and a new species

FIGURE 1. Dromilites bucklandii H. Milne Edwards, 1937. 1. Lectotype MNHN.F.B21561: (London Clay, Isle of Sheppey, Kent, United Kingdom): 1a. carapace in dorsal view, 1b. carapace in frontal view, 1c. carapace coated with ammonium chloride in dorsal view, 2. Holotype NHMUK PI IC 34026 (London Clay, Highgate, London, UK; Spencer coll.) of Dromilites simplex, nov. syn. of D. bucklandii: 2a. colored dorsal view, 2b. black and white dorsal view. Scale bars equal 10 mm. Photographs: Lilian Cazes (1) and Barry van Bakel (2).

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FIGURE 3. Dromilites belli n in Revision of Dromilites bucklandii (Crustacea, Decapoda, Brachyura): Type material revealing its real identity, a junior synonym, and a new species

FIGURE 3. Dromilites belli n. sp. type series from the Ypresian London Clay (Division B1, Kent, United Kingdom). 1. Paratype MAB.k 3583 (Seasalter, foreshore exposure) coated with ammonium chloride: 1a. carapace in dorsal view, 1b. carapace in frontal view; 2. Paratype MAB.k 3584 (Seasalter, foreshore exposure): claws; 3. Paratype MAB.k 3585 (Seasalter, foreshore exposure) (female individual): abdomen in ventral view; 4. Paratype MAB.k 3587 (Seasalter, foreshore exposure) (female individual): abdomen in ventral view; 5. Paratype MAB.k 3586 (Tankerton, foreshore exposure) (male individual): abdomen in ventral view. Scale bars equal 1cm. Photographs. Lilian Cazes (1) and Barry van Bakel (2-5).

Figure 2 in The taxonomic catalog of the Brazilian fauna: Dermaptera and Phasmatodea (Insecta), with commentaries on species list, types, authorship and distribution

Figure 2. Data on species authorship of Dermaptera: (A) demography in relation to nationality; (B) ranking of authors who described the highest numbers of earwig species, from first to last: Carlos Moreira in first place; Malcom Burr and Carl August Dohrn tied in second; Alan Brindle in third; Jean Guillaume Audinet-Serville, Alfredo Borelli, Samuel Scudder, Carl Stål, and Henrik Steinmann tied in fourth; Auguste de Bormans, William Kirby, and Joaquim Machado Filho tied in fifth.

Figure 5 in The taxonomic catalog of the Brazilian fauna: Dermaptera and Phasmatodea (Insecta), with commentaries on species list, types, authorship and distribution

Figure 5. Distribution of the publications of Phasmatodea species across time. Time gap* = period of time that had no descriptions of species; species cluster** = high amounts of species described clustered in a short period of time, between time gaps.

Figure 4 in The taxonomic catalog of the Brazilian fauna: Dermaptera and Phasmatodea (Insecta), with commentaries on species list, types, authorship and distribution

Figure 4. Distribution of the publications of Dermaptera species across time. Time gap* = period of time that had no descriptions of species.

Figure 3 in The taxonomic catalog of the Brazilian fauna: Dermaptera and Phasmatodea (Insecta), with commentaries on species list, types, authorship and distribution

Figure 3. Data on species authorship of Phasmatodea: (A) demography in relation to nationality; (B) ranking of authors who described the highest numbers of walking-sticks species, from first to last: Ludwig Redtenbacher, Salvador de Toledo Piza Jr., John O. Westwood, Karl Brunner-von Wattenwyl, and Raphael A. Heleodoro.

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Fig. 5 in The type species of Cyrtosymbole and the oldest (Famennian) cyrtosymboline trilobites

Fig. 5. Scatter plot of maximum length versus maximum width of the glabella (glabellar lobe + occipital lobe) for 105 undistorted individuals. The lectotype is marked with a black triangle.

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Fig. 1. A in The type species of Cyrtosymbole and the oldest (Famennian) cyrtosymboline trilobites

Fig. 1. A. Location of Cabrières village in the southeastern Montagne Noire, southern France; shaded areas indicate outcropping pre−Mesozoic massifs. B. Cyrtosymbole escoti bearing localities (La Tourière, La Serre and Peret) in the vicinity of Cabrières village; shaded areas indicate Devonian outcrops; solid lines indicate roads.

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Fig. 6 in The type species of Cyrtosymbole and the oldest (Famennian) cyrtosymboline trilobites

Fig. 6. Scatter plot of maximum sagittal length versus maximum width of the pygidium (excluding articulating half−ring) for 81 undistorted individuals.

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Linked collectors and determiners for: On the Aleochara subgenera Ceranota and Xenochara. IV. A revision of types, a new species, and additional records (Coleoptera: Staphylinidae: Aleocharinae).

Natural history specimen data linked to collectors and determiners held within, "On the Aleochara subgenera Ceranota and Xenochara. IV. A revision of types, a new species, and additional records (Coleoptera: Staphylinidae: Aleocharinae)". Claims or attributions were made on Bionomia by volunteer Scribes, <a href="https://bionomia.net/dataset/18b7b01a-43f9-4707-b54a-d62d02ee7d34">https://bionomia.net/dataset/18b7b01a-43f9-4707-b54a-d62d02ee7d34</a> using specimen data from the dataset aggregated by the Global Biodiversity Information Facility, <a href="https://gbif.org/dataset/18b7b01a-43f9-4707-b54a-d62d02ee7d34">https://gbif.org/dataset/18b7b01a-43f9-4707-b54a-d62d02ee7d34</a>. Formatted as a Frictionless Data package.