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Fig. 7 in A historical and integrative taxonomic account of mangrove oyster species native to the Atlantic American coast: A re-evaluation of Brazilian Crassostrea species

Fig. 7. Mean (± standard deviation) shell characters from measurements (SH, SL, SW, SH/SL, RVH/SH). Frequency of C. gasar and C. rhizophorae individuals for each category of SF (p <0.05).

Fig. 4 in A historical and integrative taxonomic account of mangrove oyster species native to the Atlantic American coast: A re-evaluation of Brazilian Crassostrea species

Fig. 4. Shell range of colors. Left valve: a – (Brownish; Bwn), b – (Yellowish; Ylw), c – (White with purple stripes; WP), d – (Whitish; Wht); Right valve: e and f – (Brownish; Bwn), g – (Yellowish; Ylw), h – (Whitish; Wht). Scale: 10 mm. Illustration by Leandro Lopes de Souza. (For interpretation of the references to color in this figure legend, the reader is referred to the Web version of this article.)

Fig. 2 in A historical and integrative taxonomic account of mangrove oyster species native to the Atlantic American coast: A re-evaluation of Brazilian Crassostrea species

Fig. 2. Conchological aspects of the left valve. Internal color: a – (purple), b – (Faintly pigmented), c and d – (white); Internal margin color: c – (purple), d – (white); Outter ornamentation of shells: e and g – (merged scales, "g" with longitudinal costae), f – (imbricate scales); A conspicuous projection of the left shell valve: h – (branchitellum). Color of adductor muscle scar: i – (white), j – (faintly pigmented), k – (purple). Scale; 10 mm. Illustration based on mangrove oysters collected in this study. Illustration by Leandro Lopes de Souza. (For interpretation of the references to color in this figure legend, the reader is referred to the Web version of this article.)

Fig. 3 in A historical and integrative taxonomic account of mangrove oyster species native to the Atlantic American coast: A re-evaluation of Brazilian Crassostrea species

Fig. 3. Shell formats: a – (Circle), b – (Obovoid), c – (Ellipsoid), d – (Elongate). Scale: 10 mm. Illustration by Leandro Lopes de Souza.

Fig. 13 in A historical and integrative taxonomic account of mangrove oyster species native to the Atlantic American coast: A re-evaluation of Brazilian Crassostrea species

Fig. 13. The χ2 test of independence of Species, MSF and MSC, based on the permutation distribution.

Fig. 21 in A historical and integrative taxonomic account of mangrove oyster species native to the Atlantic American coast: A re-evaluation of Brazilian Crassostrea species

Fig. 21. The χ2 test of independence of Species, SF, MSF and UCC, based on the permutation distribution. Legends for MSF (E Elongate, O - Ovate, R – Reniform) and UCC (S – Shallow, D – Deep).

FIGURE 2 in An unusual species of the genus Pseudohalmyrapseudes Larsen & Hansknecht, 2004 (Tanaidacea: Parapseudidae) from the mangrove swamps of the Cần Giờ Biosphere Reserve, South Vietnam

FIGURE 2. Pseudohalmyrapseudes alexeitiunovi sp. nov., coloration of live specimens, dorsal and lateral views of adult ♂♂ (above) and ♀ (below) habitus.

FIGURE 5 in An unusual species of the genus Pseudohalmyrapseudes Larsen & Hansknecht, 2004 (Tanaidacea: Parapseudidae) from the mangrove swamps of the Cần Giờ Biosphere Reserve, South Vietnam

FIGURE 5. Pseudohalmyrapseudes alexeitiunovi sp. nov., chelipeds, ♀ (a), sub-adult ♂ (b) and adult ♂ (c, d).

FIGURE 1 in An unusual species of the genus Pseudohalmyrapseudes Larsen & Hansknecht, 2004 (Tanaidacea: Parapseudidae) from the mangrove swamps of the Cần Giờ Biosphere Reserve, South Vietnam

FIGURE 1. The map of the studied area and the habitat of Pseudohalmyrapseudes alexeitiunovi sp. nov., in the mangrove swamps of the Cần Giớ Biosphere Reserve in South Vietnam: a–c—general map of the location of the study area in different scale; d—general view of the lagoon in in the cut part of the deep mangrove channel during the high level of the tide; e—same lagoon during sampling at the medium level of tide; f—same lagoon during the lowest level of the tide. Photo credits: e, f—from Tien Tran Van.

FIGURE 7 in An unusual species of the genus Pseudohalmyrapseudes Larsen & Hansknecht, 2004 (Tanaidacea: Parapseudidae) from the mangrove swamps of the Cần Giờ Biosphere Reserve, South Vietnam

FIGURE 7. Pseudohalmyrapseudes alexeitiunovi sp. nov., ♀ (a–d, f) and ♂ (e), LEMMI: a, b—pleotelson, different views; c—pleopod I; d—uropod; e—penis; f—setation of pleonites; g—pereon, dorsal view.

FIGURE 4 in An unusual species of the genus Pseudohalmyrapseudes Larsen & Hansknecht, 2004 (Tanaidacea: Parapseudidae) from the mangrove swamps of the Cần Giờ Biosphere Reserve, South Vietnam

FIGURE 4. Pseudohalmyrapseudes alexeitiunovi sp. nov., ♀: a—right mandible; b—same, incisor process; c—left mandible; d—same, incisor process; e—maxillula; f—maxille; g—maxilliped; h—endite of maxilliped.

FIGURE 3 in An unusual species of the genus Pseudohalmyrapseudes Larsen & Hansknecht, 2004 (Tanaidacea: Parapseudidae) from the mangrove swamps of the Cần Giờ Biosphere Reserve, South Vietnam

FIGURE 3. Pseudohalmyrapseudes alexeitiunovi sp. nov., ♀ (a, d, f–h) and ♂ (b, c, e): a–c—antennule; d, e—antenna; f— labrum; g—labium; h—epignath.

FIGURE 6 in An unusual species of the genus Pseudohalmyrapseudes Larsen & Hansknecht, 2004 (Tanaidacea: Parapseudidae) from the mangrove swamps of the Cần Giờ Biosphere Reserve, South Vietnam

FIGURE 6. Pseudohalmyrapseudes alexeitiunovi sp. nov., ♀: a—pereopod I; b—pereopod II; c—pereopod III; d—pereopod IV; e—pereopod V; f—pereopod VI.

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Fig. 3 in Ants nesting in red mangroves of The Gambia (West Africa)

Fig. 3 Crematogaster gambiensis André, 1889, worker [KGCOL02459]. A, frontal view. B, lateral view. © J. Lalanne

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Fig. 1 in Ants nesting in red mangroves of The Gambia (West Africa)

Fig. 1. Study area near the mouth of the Gambia River (rectangle above); six study sites (A-F below). Map data from Google Maps.

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Fig. 2 Cataulacus traegaordhi Santschi, 1914 in Ants nesting in red mangroves of The Gambia (West Africa)

Fig. 2 Cataulacus traegaordhi Santschi, 1914, worker. [KGCOL02497]. A, frontal view. B, lateral view. © J. Lalanne

Figure 24 in Nereidid polychaetes (Annelida) inhabiting the inside of decaying fronds of the mangrove palm Nypa fruticans in a tropical estuary in Malaysia, with special reference to the life history of the dominant species, Namalycastis sp.

Figure 24. Seasonal change in average salinity and temperature at six sites in Setiu Wetlands, Terengganu, in Malaysia (a), rainfall amount recorded at Bukit Berangan, Setiu, based on data from CHIRPS (Funk et al. 2019) (b), during the sampling period from September 2015 to September 2016.

Figure 21 in Nereidid polychaetes (Annelida) inhabiting the inside of decaying fronds of the mangrove palm Nypa fruticans in a tropical estuary in Malaysia, with special reference to the life history of the dominant species, Namalycastis sp.

Figure 21. Seasonal change in size–frequency histogram of mean diameters of coelomic oocytes of Namalycastis sp. collected from six sites in Setiu Wetlands, Terengganu in Malaysia via seven samplings in the period from September 2015 to September 2016. n: number of females examined.

Figure 19 in Nereidid polychaetes (Annelida) inhabiting the inside of decaying fronds of the mangrove palm Nypa fruticans in a tropical estuary in Malaysia, with special reference to the life history of the dominant species, Namalycastis sp.

Figure 19. Seasonal change in mean body width of females, males, and individuals with sex unknown in pooled samples of Namalycastis sp. collected from six sites in Setiu Wetlands, Terengganu, in Malaysia via seven samplings in the period from September 2015 to September 2016.

Figure 16 in Nereidid polychaetes (Annelida) inhabiting the inside of decaying fronds of the mangrove palm Nypa fruticans in a tropical estuary in Malaysia, with special reference to the life history of the dominant species, Namalycastis sp.

Figure 16. Relationship between body width and body length of 277 complete specimens of Namalycastis sp. collected from September 2015 to September 2016 at six sites in Setiu Wetlands, Terengganu in Malaysia (Table 1).