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Figure 1 in Morphofunctional characterization and antibacterial activity of haemocytes from Octopus vulgaris

Figure 1. Differential interference contrast micrographs showing different types of haemocytes in culture plate: (A) haemoblast-like cell without pseudopodia; (B) two hyalinocytes connecting each other with pseudopodia; (C) well-attached granulocyte showing dendritic pseudopodia formation; (D) graph showing the ratio among the three haemocyte types. Scale bar = 5 μm.

Figure 7 in Diagnosis and key for the Helina annosa-group (Diptera: Muscidae) from China, with descriptions of nine new species

Figure 7. Helina setosiannosa Xue, sp. nov. (A) Male, abdomen in dorsal view; (B) male, sternite 5 in ventral view; (C) male, cerci in posterior view; (D) male, terminalia in profile. Scale bars: A, 1 mm; B–D, 0.5 mm.

Figure 10 in Ontogeny of the deep-sea cranchiid squid Teuthowenia pellucida (Cephalopoda: Cranchiidae) from New Zealand waters

Figure 10. Development of fin shape between juvenile and sub-adult stages (stages E and F) of Teuthowenia pellucida. Specimen maturation from left to right.

Figure 8 in Ontogeny of the deep-sea cranchiid squid Teuthowenia pellucida (Cephalopoda: Cranchiidae) from New Zealand waters

Figure 8. Arm modifications in adult Teuthowenia pellucida. Brachial end organ (A) on the tips of all arms in mature females; (B) four series of small suckers on the distal tip of arms I and II in adult males. Scale bar = 1 cm.

Figure 6 in Ontogeny of the deep-sea cranchiid squid Teuthowenia pellucida (Cephalopoda: Cranchiidae) from New Zealand waters

Figure 6. Simplified diagram of eye photophores and lens from (A) anterior view and (B) ventral side of the eye in adult Teuthowenia pellucida.

Figure 4 in Morphofunctional characterization and antibacterial activity of haemocytes from Octopus vulgaris

Figure 4. Light microscopy micrographs of Octopus vulgaris haemocytes processed with enzymatic histochemistry analysis: (A) granulocytes showing a peroxidase activity localized as dark brown deposits; (B) haemoblast-like cells with phenol oxidase activity; (C) hyalinocytes with phenol oxidase activity; (D) granulocytes showing phenol oxidase activity. Scale bar = 5 μm.

Figure 4 in Ontogeny of the deep-sea cranchiid squid Teuthowenia pellucida (Cephalopoda: Cranchiidae) from New Zealand waters

Figure 4. Schematic diagram of Teuthowenia pellucida tentacle showing paired zig-zag sucker pattern on stalk, visible from Stage D onwards.

Figure 2 in Ontogeny of the deep-sea cranchiid squid Teuthowenia pellucida (Cephalopoda: Cranchiidae) from New Zealand waters

Figure 2. Development of Teuthowenia pellucida eyes through ontogeny showing both anterior (right) and lateral (left) perspective. Eye presented from (A) stage A; (B) stage B; (C) stage C; (D) stage D; (E) stage E and F; (F) adult (anterior); (G) adult (ventral). Scale bar = 1 mm.

Figure 3 in Morphofunctional characterization and antibacterial activity of haemocytes from Octopus vulgaris

Figure 3. Light microscopy micrographs of haemocytes stained with Giemsa/May–Grünwald stain: (A) acidophilic haemoblast-like cells (arrowheads) and granulocytes with acidophilic cytoplasm and cells (arrows); (B) hyalinocytes with basophilic nucleus and cytoplasm filled with vacuoles and few granules; (C) granulocytes cells with basophilic cytoplasm. Scale bar 5 μm.

Figure 12 in Ontogeny of the deep-sea cranchiid squid Teuthowenia pellucida (Cephalopoda: Cranchiidae) from New Zealand waters

Figure 12. Difference in visible rachis shape at anterior dorsal midline of (A) Teuthowenia; (B) Megalocranchia; (C) Liguriella (ML range: 17–29 mm).

Figure 6 in Diagnosis and key for the Helina annosa-group (Diptera: Muscidae) from China, with descriptions of nine new species

Figure 6. Helina nivimonta Xue, sp. nov. (A) Male, abdomen in dorsal view; (B) male, sternite 5 in ventral view; (C) male, cerci in posterior view; (D) male, terminalia in profile. Scale bars: A, 1 mm; B, 0.5 mm; C, D, 0.2 mm.

Figure 2 in The contribution of molecular data to our understanding of cephalopod evolution and systematics: a review

Figure 2. Polyploidy scenario suggested by and reproduced from Bonnaud et al. (2004). Updated diploid chromosome numbers (see Table 2) for the various branches are now Nautiloidea 52; Octopoda 56–60; Sepiolida 74; Sepiida 48–112; Myopsida 86–92 (?22-?172).

Figure 6 in Morphology and morphometry of Doryteuthis plei (Cephalopoda: Loliginidae) statoliths from the northern shelf off São Paulo, southeastern Brazil

Figure 6. Comparison between squid statoliths at the same stage of maturity. (A) Doryteuthis plei; (B) Doryteuthis sanpaulensis. The bluish appearance of the D. sanpaulensis statolith is probably due to refractive properties, because it is more transparent than the D. plei statolith.

Figure 3 in Observations on age and reproduction of the oceanic squid Ancistrocheirus lesueurii (d'Orbigny, 1842) (Cephalopoda: Ancistrocheiridae)

Figure 3. Ancistrocheirus lesueurii. (A) Statolith section of a mature intersexual male (ML 275 mm) in which 761 increments could be counted. The areas in boxes are enlarged in B, C and D, where B is the nucleus, C shows regular increments past the mid part of the rostrum and D shows the increments in the periphery of the rostrum.

Figure 6 in The contribution of molecular data to our understanding of cephalopod evolution and systematics: a review

Figure 6. Relationships among Sepiida. (A) Consensus tree based on 12S rRNA, 16S rRNA, cytochrome oxidase subunit II (Bonnaud et al. 2006); (B) maximum likelihood tree of cytochrome oxidase subunit I, cytochrome b and ND5 combined (Yoshida et al. 2010); (C) whole evidence approach using four to ten genes (Lindgren et al. 2012). Trees redrawn from original sources.

Figure 7 in The contribution of molecular data to our understanding of cephalopod evolution and systematics: a review

Figure 7. Relationships within Onychoteuthidae. (A) Neighbour-joining tree based on 16S ribosomal RNA (Bonnaud et al. 1998); (B) maximum likelihood tree of five genes (see text) combined (Lindgren 2010); (C) maximum likelihood tree based on whole evidence approach using four to ten genes (Lindgren et al. 2012). All trees redrawn from original sources. Nomenclature uses systematic revision of Bolstad (2010).

Figure 4 in Morphology and morphometry of Doryteuthis plei (Cephalopoda: Loliginidae) statoliths from the northern shelf off São Paulo, southeastern Brazil

Figure 4. Morphometric values of the Doryteuthis plei statoliths into categories (M) males, (F) females, (I) immature, (II) maturing, (III) mature and (IV) spent by statolith measures (SL) statolith length, (DL) dome length, (ÂR) angle of the rostrum and (ÂD) angle of the dome.

Figure 1 in Intraspecific larval aggression in two species of Hyperini (Coleoptera: Curculionidae)

Figure 1. The number of fights observed in experiments with groups of Hypera postica larvae of various instars (L1–L4), in the presence (plain boxes) or absence (hatched boxes) of food (leaves of Medicago sativa). Filled circles and squares indicate the mean, boxes indicate confidence intervals, whiskers show the non-outlier range and empty circles represent outliers.

Figure 2 in Intraspecific larval aggression in two species of Hyperini (Coleoptera: Curculionidae)

Figure 2. The number of fights observed in experiments with mixed-instar groups of Hypera postica larvae in the presence or absence of food (leaves of Medicago sativa). Filled circles indicate the mean value, boxes show the confidence intervals, whiskers represent the nonoutlier range and empty circles represent outliers.

Figure 2 in A new genus with two new species of mesosciophilids from the Middle Jurassic of China (Diptera: Nematocera: Mesosciophilidae)

Figure 2. Similsciophila singularis gen. et sp. nov., paratype, CNU-DIP-NN2011147 p/c. (A) Photograph of habitus (lateral aspect), part; (B) photograph of counterpart; (C) line drawing of holotype, counterpart; (D) photograph of antennae; (E) photograph of antennae with alcohol; (F) line drawing of antennae.