Find research datasets worth reusing

Figure 5 in The diverse Grania fauna (Clitellata: Enchytraeidae) of the Esperance area, Western Australia, with descriptions of two new species

Figure 5. (A) Grania ersei Coates, 1990, chaetae from different segments as indicated by Roman numerals. (B–D) Grania quaerens sp. n.: (B) chaetae from different segments as indicated by Roman numerals; (C) spermatheca; (D) lateral view of the penial apparatus. (C) and (D) shown to the same scale. l, lateral chaeta; v, ventral chaeta.

Figure 9 in The diverse Grania fauna (Clitellata: Enchytraeidae) of the Esperance area, Western Australia, with descriptions of two new species

Figure 9. Grania vacivasa Coates and Stacey, 1993. (A) Ventral chaeta of segment XXIX; (B) dorsolateral view of cephalic region; (C, D) pygidium in lateral (C) and ventral (D) views, showing expanded rectal ampulla; (E) caudal segments showing large sponge spicules inside gut lumen.

Figure 8 in The diverse Grania fauna (Clitellata: Enchytraeidae) of the Esperance area, Western Australia, with descriptions of two new species

Figure 8. (A, B) Grania sperantia sp. n. (A) Chaetae from different segments as indicated by Roman numerals (all ventral chaetae); (B) dorsal view of the spermatheca and pharyngeal glands of segment V; (C) Grania vacivasa Coates and Stacey, 1993, chaetae from different segments as indicated by Roman numerals (all ventral chaetae).

Figure 7 in The diverse Grania fauna (Clitellata: Enchytraeidae) of the Esperance area, Western Australia, with descriptions of two new species

Figure 7. Grania sperantia sp. n. (A, B) Cephalic region in lateral (A) and dorsal (B) views, showing the head organ and its hollowed inclusions; (C) ventral view of clitellum; (D) detail of the anterior part of clitellum, showing (above) the two anterior sub-bands of rectangular hyaline cells, intermingled or not with small refringent cells, and (below) the middle band made of hyaline and pale granular, polygonal cells; (E) ventrolateral view of penial bulb; (F) ventral chaeta of segment XXXVII, turned somewhat frontally; (G, H) pygidium in lateral (G) and ventral (H) views, showing rectal ampulla.

Figure 4 in The diverse Grania fauna (Clitellata: Enchytraeidae) of the Esperance area, Western Australia, with descriptions of two new species

Figure 4. (A–C) Grania dolichura Rota and Erséus, 2000: (A) coelomocytes; (B) cephalic region, dorsolateral view; (C) ventral chaeta of segment LXVII. (D–G) Grania ersei Coates, 1990: (D) tip of cephalic region in dorsolateral view, showing a shallow optical section of the prostomium and the typical bilobed outline of the head organ; (E) cephalic region of a different specimen. Deeper optical section through the head organ showing the location of inclusions inside the ''empty'' compartments; (F) coelomocytes; (G) terminal tract of the vas deferens and the enclosed penial stylet in an unusual loose state; the stylet length is more than twice the length of segment XII.

Figures 14–19 in Suspended mummies in Aleiodes species (Hymenoptera: Braconidae: Rogadinae) with descriptions of six new species from western Uganda based largely on DNA sequence data

Figures 14–19. Automontage photographs of features of the Aleiodes buzurae-group. (14) Aleiodes kasenenei sp. n., habitus; (15)–(19) Aleiodes kanyawarensis sp. n., habitus, face, mesosoma, wings and metasoma, respectively.

Figure 3 in Suspended mummies in Aleiodes species (Hymenoptera: Braconidae: Rogadinae) with descriptions of six new species from western Uganda based largely on DNA sequence data

Figure 3. Bootstrap consensus tree from analysis of CO1 sequence data for Aleiodes reared from suspended mummies in Uganda plus another member of the A. buzurae-group and outgroups.

Figures 20–25 in Suspended mummies in Aleiodes species (Hymenoptera: Braconidae: Rogadinae) with descriptions of six new species from western Uganda based largely on DNA sequence data

Figures 20–25. Automontage photographs of features of Aleiodes trevelyanae sp. n. (20)–(24) Habitus, face, metasoma, mesosoma and wings of holotype; (25) metasoma of paratype.

Figure 9 in The genera Urticina and Cribrinopsis (Anthozoa: Actiniaria) from the north-western Pacific

Figure 9. Urticina grebelnyi sp. nov. (A) Cross-sections of the marginal sphincter; (B) cross-section of the tentacle; (C) mesenteries of the first to fourth orders, gonads on mesenteries of the fourth order.

Figure 3 in The genera Urticina and Cribrinopsis (Anthozoa: Actiniaria) from the north-western Pacific

Figure 3. Cribrinopsis olegi sp. nov. (A) Cross-sections of the marginal sphincter; (B) cross-section of the tentacle; (C) mesenteries of the first to fifth orders, gonads on one directive and one mesentery of the second order.

Figures 10–13 in Suspended mummies in Aleiodes species (Hymenoptera: Braconidae: Rogadinae) with descriptions of six new species from western Uganda based largely on DNA sequence data

Figures 10–13. Automontage photographs of features of Aleiodes busutai sp. n., habitus, head lateral aspect, metasoma and mesosoma, respectively.

Figure 1 in The genera Urticina and Cribrinopsis (Anthozoa: Actiniaria) from the north-western Pacific

Figure 1. Cribrinopsis albopunctata sp. nov. (A) Cross-sections of the marginal sphincter; (B) cross-section of the tentacle; (C) mesenteries of the first, second and third orders, gonads on one mesentery of the first and one mesentery of the third order, large larva is between the mesenteries of the third order.

Figure 11 in The genera Urticina and Cribrinopsis (Anthozoa: Actiniaria) from the north-western Pacific

Figure 11. Comparison of size ranges of large basitrichs in tentacles (thin lines) and in actinopharynx (thick lines) of some species assigned to Urticina and Cribrinopsis (*literature data).

Figure 2 in Suspended mummies in Aleiodes species (Hymenoptera: Braconidae: Rogadinae) with descriptions of six new species from western Uganda based largely on DNA sequence data

Figure 2. Phylogram from analysis of CO1 DNA sequence data for individuals of the A. buzurae-group and related species, and also multiple representatives of four European species for comparison.

Figure 1 in Suspended mummies in Aleiodes species (Hymenoptera: Braconidae: Rogadinae) with descriptions of six new species from western Uganda based largely on DNA sequence data

Figure 1. Photograph of a suspended mummy showing J-shaped configuration with silk thread (arrowed) arising near larval mouth.

Figure 4 in Suspended mummies in Aleiodes species (Hymenoptera: Braconidae: Rogadinae) with descriptions of six new species from western Uganda based largely on DNA sequence data

Figure 4. Selected contiguous fragment of the CO1 gene in individuals of the Aleiodes buzurae-group from Uganda and Kenya with bold characters indicating substitutions. Asterisks show phylogenetically informative substitutions at species level; exclamation marks show apomorphies for individual species in the buzarae group and $ sites that have both unique and informative variation.

Figure 5 in Ectosymbionts of the non-indigenous Asian shore crab, Hemigrapsus sanguineus (Decapoda: Varunidae), in the western north Atlantic, and a search for its parasites

Figure 5. (A) Dorsal view of Carcinus maenas male (56.4 mm CW; injury to carpus of right cheliped) with five barnacles Semibalanus balanoides located in grooves around the mesogastric region of the carapace. Small colonies of Conopeum tenuissimum are scattered on the carapace. Arrow points to the opening of a Sabellaria vulgaris tube in the right hepatic area. (B) Dorsal view of Panopeus herbstii female (23.5 mm CW; right cheliped and two left walking legs missing) with large Conopeum tenuissimum colony on right side spanning frontal, progastric, hepatic, and branchial areas; another colony on carpus of the left cheliped. One large colony of Alcyonidium albescens on left side (arrow).

Figure 3 in Ectosymbionts of the non-indigenous Asian shore crab, Hemigrapsus sanguineus (Decapoda: Varunidae), in the western north Atlantic, and a search for its parasites

Figure 3. (A) Frequency of Conopeum tenuissimum versus CW (1.0 mm classes) of Hemigrapsus sanguineus collected March and April 2006 at Townsends Inlet, New Jersey. Open bars, total crabs examined (n5281); shaded bars, crabs with bryozoans (n5156). (B) Number of colonies of Conopeum tenuissimum (n5638) on specimens of Hemigrapsus sanguineus (n5119; 1.0 mm CW classes) collected March 2006 at Townsends Inlet, New Jersey. Regression equation: y (no. colonies)527.518+0.681x (CW); r250.281, p 0.0001, n5119.

Figure 2 in Ectosymbionts of the non-indigenous Asian shore crab, Hemigrapsus sanguineus (Decapoda: Varunidae), in the western north Atlantic, and a search for its parasites

Figure 2. Ventral view of Hemigrapsus sanguineus female (26.1 mm CW; same crab as Figure 1B) with a gaping abdomen caused by the accumulation of young blue mussels Mytilus edulis attached to the pleopods (white arrow shows largest mussel, 9.5 mm long). Colonies of the calcareous bryozoan Conopeum tenuissimum present on many of the pereopods. Black arrow points to the polychaete Spirorbis sp.

Figure 4 in Ectosymbionts of the non-indigenous Asian shore crab, Hemigrapsus sanguineus (Decapoda: Varunidae), in the western north Atlantic, and a search for its parasites

Figure 4. Percentages of colonies of Conopeum tenuissimum at various locations on the carapace of Hemigrapsus sanguineus based on 336 colonies from 134 crabs (Table III) collected 29 March 2006 and 26 April 2006 at Townsends Inlet. Anterolaterally are hepatic areas, posterolaterally are branchial areas; numbers in parentheses are for colonies that span the hepatic-branchial regions. Medially from anterior to posterior are frontal, progastric, mesogastric, cardiac, and intestinal locations.