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FIGURE 18 in A taxonomic review of the anilline genus Zeanillus Jeannel (Coleoptera: Carabidae: Bembidiini) of New Zealand, with descriptions of seven new species, re-classification of the species, and notes on their biogeography and evolution
FIGURE 18. Map of southern half of South Island, New Zealand, showing positions of locality records for the species of Zeanillus. A: white circles, Z. phyllobius; green circles, Z. punctigerus; red circles, Z. nunni; blue diamond, Z. pellucidus; green diamond, Z. pallidus. B: white triangles, Z. brouni; green triangles, Z. nanus; red triangles, Z. lescheni; yellow triangle, Z. carltoni; black triangle, Z. montivagus. Elevation scale bars are given in meters.
FIGURE 3 in A taxonomic review of the anilline genus Zeanillus Jeannel (Coleoptera: Carabidae: Bembidiini) of New Zealand, with descriptions of seven new species, re-classification of the species, and notes on their biogeography and evolution
FIGURE 3. Line drawings of mandibles of Zeanillus species. A–B Z. phyllobius: dorsal aspect of left and right mandibles, respectively. C–D Z. pallidus: dorsal aspect of left and right mandibles, respectively. E–F Z. pellucidus: dorsal aspect of left and right mandibles, respectively. G–H Z. lescheni: dorsal aspect of left and right mandibles, respectively. Legend: artanterior retinacular tooth; it—incisor tooth; mt—molar tooth; prt—posterior retinacular tooth; tr—terebral ridge; tt—terebral tooth. Scale bars = 0.1mm.
FIGURE 2 in Taxonomic status of Andersen's fruit-eating bat (Artibeus jamaicensis aequatorialis) and revised classification of Artibeus (Chiroptera: Phyllostomidae)
FIGURE 2. Unrooted neighbor-joining phylogram based on 414 AFLP bands. Numbers along branches indicate bootstrap support values (top score) and Bayesian posterior probabilities (bottom score). Bold clade identifies specimens traditionally recognized as Artibeus jamaicensis aequatorialis.
FIGURE 3 in Taxonomic status of Andersen's fruit-eating bat (Artibeus jamaicensis aequatorialis) and revised classification of Artibeus (Chiroptera: Phyllostomidae)
FIGURE 3. Map of the distribution of Artibeus aequatorialis. Star indicates the type locality of A. aequatorialis (Zaruma [3°40'60"S, 79°37'0"W], Ecuador). The distributional range is based on literature references (hollow squares; Andersen 1906 and Marques-Aguiar 2008) and specimens examined in the Species Account (star and solid squares). The northernmost (western Colombia; Valle del Cauca, Cali [3°26'14"N, 76°31'21"W], and Rio Raposo [3°43'0"N, 77°7'60"W]) and southernmost (western Peru; Tumbes, Faical [3°44'57"S, 80°45'2"W]) extent of A. aequatorialis remains to be defined. Shaded areas represent areas of the Andes Mountains higher than 1800 meters.
FIGURE 10 in A taxonomic review of the anilline genus Zeanillus Jeannel (Coleoptera: Carabidae: Bembidiini) of New Zealand, with descriptions of seven new species, re-classification of the species, and notes on their biogeography and evolution
FIGURE 10. SEM illustrations of structural features of legs of Zeanillus species, various aspects. A–E right protarsus and protibia, ventral aspect: A, D–E—females; B–C—males. A—Z. phyllobius; B—Z. punctigerus; C—Z. pellucidus; D—Z. pallidus; E—Z. brouni. F–G, H, J right and I, K left mesotibia: F—Z. phyllobius, ventral aspect; G—Z. punctigerus, ventral aspect; H—Z. pellucidus, medial aspect; I—Z. pallidus, ventral aspect; J—Z. lescheni, ventral aspect; K—Z. brouni, ventral aspect. L–M, O right and N, P–Q left metatibia: L—Z. phyllobius, ventral aspect; M—Z. punctigerus, ventral aspect; N—Z. pellucidus, medial aspect; O—Z. pallidus, ventral aspect; P—Z. lescheni, ventral aspect; Q—Z. brouni, medial aspect. Legend: ac—antenna cleaner; as—adhesive seta; asp—anterior spur; asr—anterior setal row; cls—clip seta; msb—mesotibial brush; msms—mesotibial modified seta; mss—mesotibial spur; mtb—metatibial brush; mtms—metatibial modified seta; mtsmetatibial spur; psp—posterior spur; psr—posterior setal row; sb—setal band; ta1–ta4—tarsomeres 1–4. Scale bars = 0.05mm.
FIGURE 9 in A taxonomic review of the anilline genus Zeanillus Jeannel (Coleoptera: Carabidae: Bembidiini) of New Zealand, with descriptions of seven new species, re-classification of the species, and notes on their biogeography and evolution
FIGURE 9. SEM illustrations of pygidium and apex of elytra, dorsal aspect, of Zeanillus species. A—Z. phyllobius; B—Z. punctigerus; C—Z. pellucidus; D—Z. lescheni. Legend: ea—apex of right elytron; ed8—apical seta; pgd—pygidium; suelytral suture. Scale bars = 0.05 mm.
FIGURE 6 in A taxonomic review of the anilline genus Zeanillus Jeannel (Coleoptera: Carabidae: Bembidiini) of New Zealand, with descriptions of seven new species, re-classification of the species, and notes on their biogeography and evolution
FIGURE 6. SEM illustrations of prothorax, ventral aspect, of Zeanillus species. A—Z. phyllobius; B—Z. punctigerus; C—Z. pallidus; D—Z. pellucidus; E—Z. lescheni; F—Z. brouni. Legend: pas—prosternal ambulatory seta; pep—proepipleuron; pes—proepisternum; prcx—procoxa; ps—prosternum; psp—prosternal intercoxal process. Scale bars = 0.1mm.
FIGURE 8 in A taxonomic review of the anilline genus Zeanillus Jeannel (Coleoptera: Carabidae: Bembidiini) of New Zealand, with descriptions of seven new species, re-classification of the species, and notes on their biogeography and evolution
FIGURE 8. SEM illustrations of chaetotaxy of elytra, dorso-lateral aspect, of Zeanillus species. A—Z. punctigerus; B—Z. pallidus; C—Z. pellucidus; D—Z. lescheni. Legend: ed2—scutellar seta; ed3—1st discal seta; ed4–5—2nd discal seta; ed6–7— 3d discal seta; ed8—apical seta; eo1–9—setae 1–9 from the umbilical series; smes—subapical marginal elytral seta; sssubapical sinuation. Scale bars = 0.2 mm.
FIGURE 5 in A taxonomic review of the anilline genus Zeanillus Jeannel (Coleoptera: Carabidae: Bembidiini) of New Zealand, with descriptions of seven new species, re-classification of the species, and notes on their biogeography and evolution
FIGURE 5. SEM illustrations of pronotum, dorsal aspect, of Zeanillus species. A—Z. phyllobius; B—Z. punctigerus; C—Z. pallidus; D—Z. pellucidus; E—Z. lescheni; F—Z. nanus. Legend: aps—apicolateral pronotal seta; bdt—basilateral pronotal denticle; bs—basilateral pronotal seta; bsn—basilateral pronotal sinuation; ed2—scutellar seta; ls—midlateral pronotal seta; mg—marginal pronotal gutter; sct—scutellum. Scale bars = 0.1 mm.
FIGURE 4 in A taxonomic review of the anilline genus Zeanillus Jeannel (Coleoptera: Carabidae: Bembidiini) of New Zealand, with descriptions of seven new species, re-classification of the species, and notes on their biogeography and evolution
FIGURE 4. SEM illustrations of labial complex, ventral aspect, of Zeanillus species. A—Z. phyllobius; B—Z. punctigerus; C—Z. pallidus; D—Z. pellucidus; E—Z. lescheni; F—Z. brouni. Legend: alms—anterolateral mental seta; gsc—glossal sclerite; lms—lateral mental seta; lss—lateral submental seta; m—mentum; mp3—maxillary palpomere 3; mp4—maxillary palpomere 4; mt—mental tooth; mss—mental-submental suture; pms—paramedial mental seta; prss—primary basal submental seta; sm—submentum. Scale bars = 0.1 mm.
FIGURE 2 in A taxonomic review of the anilline genus Zeanillus Jeannel (Coleoptera: Carabidae: Bembidiini) of New Zealand, with descriptions of seven new species, re-classification of the species, and notes on their biogeography and evolution
FIGURE 2. SEM illustrations of chaetotaxy of head and pronotum, dorso-lateral aspect, of Zeanillus species. A—Z. phyllobius; B—Z. pallidus; C—Z. pellucidus; D—Z. lescheni. Legend: aps—apicolateral pronotal seta; cs—clypeal seta; fsfrontal seta; ls—midlateral pronotal seta; pos—postorbital seta; ssa—anterior supraorbital seta; ssp—posterior supraorbital seta. Scale bars = 0.1 mm.
FIGURE 1 in A taxonomic review of the anilline genus Zeanillus Jeannel (Coleoptera: Carabidae: Bembidiini) of New Zealand, with descriptions of seven new species, re-classification of the species, and notes on their biogeography and evolution
FIGURE 1. SEM illustrations of head, dorsal aspect, of Zeanillus species. A—Z. phyllobius; B—Z. punctigerus; C—Z. pallidus; D—Z. pellucidus; E—Z. lescheni; F—Z. nanus. Legend: cl—clypeus; cs—clypeal seta; fcc—fronto-clypeal carina; fs—frontal seta; lb—labrum; mp3—maxillary palpomere 3; mp4—maxillary palpomere 4; pos—postorbital seta; ssa—anterior supraorbital seta; ssp—posterior supraorbital seta. Scale bars = 0.1 mm.
Fig. 1 in Molecular phylogeny of Geoplaninae (Platyhelminthes) challenges current classification: proposal of taxonomic actions
Fig. 1 Scheme of the phylogenetic relationships of the main groups of land planarians after Álvarez-Presas et al. (2008) using Sluys et al. (2009) nomenclature.
Fig. 3 in Molecular phylogeny of Geoplaninae (Platyhelminthes) challenges current classification: proposal of taxonomic actions
Fig. 3 Phylogenetic tree inferred from the concatenated data set by maximum likelihood (ML). Squares at nodes indicate the presence and/ or level of support of the node under the different parameter schemes as sketched in the legend; black indicates maximum support. Symbols over the nodes denote ≥ 95% bootstrap support obtained in the ML (bluish triangles) and maximum posterior probability values (1) in Bayesian inference analyses (orangish circles). Numbers following species names refer to the accession numbers of the specimens deposited in the section Platyhelminthes of the MZUSP (MZUSP PL). The notation p indicates the species pictured on the right side (pictures not to scale). Scale bar is given in number of substitutions per site.
Fig. 1 in Molecular phylogeny of Geoplaninae (Platyhelminthes) challenges current classification: proposal of taxonomic actions
Fig. 1 Scheme of the phylogenetic relationships of the main groups of land planarians after Álvarez-Presas et al. (2008) using Sluys et al. (2009) nomenclature.
Figure 3 in Taxonomic classification of the reef coral family Lobophylliidae (Cnidaria: Anthozoa: Scleractinia)
Figure 3. Micromorphology and microstructure of thickening deposits in Lobophylliidae. (A–E) Acanthastrea echinata (Dana, 1846); UNIMIB PFB201, Duad Island, Papua New Guinea. Microtuberculate texture was observed on surfaces of skeletal structures: overall (scanning electron microscopy; A); enlarged view of septal teeth that, in addition to granulations corresponding to centres of rapid accretion (blue arrows; B), shows microgranulation texture (red arrow and circle; C). Tips of these microtubercules correspond to slender bundles of fibres (red arrow and dashed lines) that form thickening deposits (regular growth bands marked with yellow arrows; polished and etched section, D; transverse thin section under polarized light, E). (F–K) the same microstructure of thickening deposits was observed in other lobophylliids (red arrow and dashed lines), suggesting clade-specific biomineralization control of formation. Similar structural organisation of thickening deposits may be affected by early diagenetic and/or bioerosional processes. (F) Homophyllia bowerbanki (Milne Edwards & Haime, 1857); MTQ MH019, Lord Howe Island, Australia. (G) Homophyllia hillae (Wells, 1955) (= Homophyllia bowerbanki); MTQ MH046, north Noddy Island, Lord Howe Island, Australia. (H) Cynarina lacrymalis (Milne Edwards & Haime, 1849a); IRD HS1604, Banc Gail, New Caledonia. (I) Lobophyllia costata (Dana, 1846); UNIMIB GA024, Gambier Islands, French Polynesia. (J) Echinophyllia orpheensis Veron & Pichon, 1980; MTQ 6821, Little Pioneer Bay, Orpheus Island, Palm Islands, Australia. (K) Oxypora lacera (Verrill, 1864); UNIMIB DJ155, Djibouti.
Figure 11. Micromussa Veron, 2000 in Taxonomic classification of the reef coral family Lobophylliidae (Cnidaria: Anthozoa: Scleractinia)
Figure 11. Micromussa Veron, 2000, has discrete corallites with double walls, medium-size (4–15 mm) and mediumrelief (3–6 mm) calices, septa in three cycles (24–36 septa), and well-developed epitheca. Septal teeth with medium height (0.3–0.6 mm) and spacing (0.3–1.0 mm), equally shaped between first- and third-order septa, equally sized between wall and septum, strong (pointed) granules, and smooth interarea. Walls formed by dominant paratheca and partial septotheca, with strong costa centre clusters. (A) Micromussa amakusensis (Veron, 1990), type species of Micromussa; macromorphology, holotype MTQ G32485, Amakusa Islands, Japan. (B, C) Micromussa indiana Benzoni & Arrigoni in Arrigoni et al., 2016a; micromorphology (scanning electron microscopy; B) and microstructure (transverse thin section; C), hypotype UF 457, Oman. (D–F) Micromussa multipunctata (Hodgson, 1985); macromorphology (D), micromorphology (E), and microstructure (F), hypotype UP P1L02161, Talim Point, Batangas, Philippines.
Figure 2 in Taxonomic classification of the reef coral family Lobophylliidae (Cnidaria: Anthozoa: Scleractinia)
Figure 2. Phylogenetic reconstructions of the reef coral family Lobophylliidae with Merulinidae as outgroup. Molecular subclades within Lobophylliidae are differentiated by colour (Arrigoni et al., 2015). (A) strict consensus of 18 maximum parsimony trees based on histone H3, internal transcribed spacers, and cytochrome c oxidase subunit I. Numbers adjacent to branches show support values (upper: maximum likelihood bootstrap ≥ 50, Bayesian posterior probability ≥ 0.9; lower: maximum parsimony bootstrap ≥ 50). (B) strict consensus of 17 maximum parsimony trees based on 46 morphological characters, with numbers indicating support (upper: Bremer decay index ≥ 2; lower: maximum parsimony bootstrap ≥ 50).
Figure 7 in Taxonomic classification of the reef coral family Lobophylliidae (Cnidaria: Anthozoa: Scleractinia)
Figure 7. Cynarina Br€ uggemann, 1877, is solitary, with discrete corallites, large (> 15 mm) and high-relief (> 6 mm) calices, septa in ≥ 4 cycles (≥ 48 septa), and weak/moderate septal lobes. Septal teeth are tall (> 0.6 mm) and widely spaced (> 1 mm), unequally shaped between first- and third-order septa, unequally sized between wall and septum, with palisade interarea. Walls formed by dominant paratheca and partial septotheca, with strong costa centre clusters and medial lines. (A–F) Cynarina lacrymalis (Milne Edwards & Haime, 1849a), type species of Cynarina; macromorphology, Cynarina savignyi Br € uggemann, 1877, syntype of Cynarina NHMUK (unlabelled lot), Gulf of Suez, Red Sea (A; photo by N. Santodomingo); micromorphology (scanning electron microscopy; B) and microstructure (transverse thin section; C), hypotype USNM 93865, Madang, Papua New Guinea; macromorphology (D), micromorphology (E), and microstructure (F), hypotype USNM 93862, Madang, Papua New Guinea.
Figure 10 in Taxonomic classification of the reef coral family Lobophylliidae (Cnidaria: Anthozoa: Scleractinia)
Figure 10. Homophyllia Br€ uggemann, 1877, has discrete corallites with fused walls, large (> 15 mm) and high-relief (> 6 mm) calices, septa in ≥ 4 cycles (≥ 48 septa), and well-developed epitheca. Septal teeth are tall (> 0.6 mm) and widely spaced (> 1 mm), equally shaped between first- and third-order septa, equally sized between wall and septum, with uniformly distributed granules, and smooth interarea. Walls formed by dominant paratheca and partial septotheca, with strong costa centre clusters. (A–C) Homophyllia australis (Milne Edwards & Haime, 1849a), type species of Homophyllia; macromorphology, syntype NHMUK 1840.11.30.77, Port Lincoln, South Australia (A; photo by H. Taylor); micromorphology (scanning electron microscopy; B) and microstructure (transverse thin section; C), hypotype USNM 85709, Sir Joseph Banks Group, South Australia. (D–F) Homophyllia bowerbanki (Milne Edwards & Haime, 1857); macromorphology, holotype MNHN scle850, Australia (D); micromorphology (E) and microstructure (F), hypotype IRD HS3285, New Caledonia. (G–I) Homophyllia hillae (Wells, 1955) (=Homophyllia bowerbanki); macromorphology, holotype QM F17943, Moreton Bay, Australia (G); micromorphology (H) and microstructure (I), hypotype USNM 91198, Lord Howe Island, Australia.
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