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Figures 13-22 from: Grego J (2018) First record of subterranean rissoidean gastropod assemblages in Southeast Asia (Mollusca, Gastropoda, Pomatiopsidae). Subterranean Biology 25: 9-34. https://doi.org/10.3897/subtbiol.25.23463

Figures 13-22 Representatives of the genus Thamkhondonia gen. n. 13–14 Thamkhondonia moureti sp. n. (holotype NHMUK 20180005) 15–18 T. vacquiei sp. n. (15–16 holotype NHMUK 20180006 17–18 paratype 1 coll. Grego F0875) 19–22 T. smidai sp. n. (19–20 holotype NHMUK 20180007 21–22 paratype 1 coll. Grego F0876).

Figures 23-48 from: Grego J (2018) First record of subterranean rissoidean gastropod assemblages in Southeast Asia (Mollusca, Gastropoda, Pomatiopsidae). Subterranean Biology 25: 9-34. https://doi.org/10.3897/subtbiol.25.23463

Figures 23-48 Representatives of the genus Tricula, Benson, 1843. 23–24 Tricula valenasi sp. n. (holotype NHMUK 20180008) 25–28 T. lenahani sp. n. (holotype NHMUK 201800010) 29–32 T. spelaea sp. n. (holotype NHMUK 20180011) 33–36 T. davisi sp. n. (holotype NHMUK 20180009) 37–38 T. reischuetzorum sp. n. (holotype NHMUK 20180012) 39–42 T. phasoungensis sp. n. (39–40 holotype NHMUK 20180013 41–42 paratype 2 coll. Grego F0881) 43–44 T. bannaensis sp. n. (holotype NHMUK 20180014) 45–48 T viengthongensis sp. n. (45–46 holotype NHMUK 20180015 47–48 paratype 1 coll. Grego F0904).

Figures 3-12 from: Grego J (2018) First record of subterranean rissoidean gastropod assemblages in Southeast Asia (Mollusca, Gastropoda, Pomatiopsidae). Subterranean Biology 25: 9-34. https://doi.org/10.3897/subtbiol.25.23463

Figures 3-12 Representatives of the genus Pseudoiglica gen. n. 3–6 Pseudoiglica pseudoiglica sp. n. (3–4 holotype NHMUK 20180001 5–6 paratype 1 coll. Grego F0871) 7–8 P. olsavskyi sp. n. (holotype NHMUK 20180003) 9–10 P. kameniari sp. n. (holotype NHMUK 20180002) 11–12 P. phonsavanica sp. n. (holotype NHMUK 20180004).

Figure 1 from: Grego J (2018) First record of subterranean rissoidean gastropod assemblages in Southeast Asia (Mollusca, Gastropoda, Pomatiopsidae). Subterranean Biology 25: 9-34. https://doi.org/10.3897/subtbiol.25.23463

Figure 1 Map of sampling localities in Laos. 1–3 Khammouane: Tham Khon Dôn Cave 1 Earthquake Dome, Type locality (LT) of Pseudoiglica pseudoiglica gen. n., sp. n., P. olsavskyi n .sp., P. kameniari sp. n., Thamkhondonia moureti gen. n., sp. n., T. vacquiei sp. n., T. smidai sp. n., Tricula valenasi sp. n., T. davisi sp. n., T. spelaea sp. n., T. lenahani sp. n. and T. bannaensis sp. n. 2 Entrance passage 3 Source of Nam Dôn River 4 Khammouane: Tham Pha Soung Cave, Frog Lake, LT of Tricula phasoungensis sp. n. 5 Khammouane Cave Na Li, LT of Tricula reischuetzorum sp. n. 6 Bolikhamsay, 16 km W Vieng Thong, LT of Tricula viengthongensis sp. n. 7, Xianghouan: Ban Nadom Village, LT of Pseudoiglica phonsavanica sp. n.

Figure 2 from: Grego J (2018) First record of subterranean rissoidean gastropod assemblages in Southeast Asia (Mollusca, Gastropoda, Pomatiopsidae). Subterranean Biology 25: 9-34. https://doi.org/10.3897/subtbiol.25.23463

Figure 2 Photos of sites where subterranean gastropods were found. A Khammouane: main entrance of Tham Khon Dôn Cave with source of Nam Dôn River (2 in Fig. 1) B Earthquake Dome in cave Tham Khon Dôn (1 in Fig. 1) C Mount Pha Kouankaohong with entrance of Tham Khon Dôn cave at its foot D Bolikhamsay, travertine cascades below the LT of Tricula viengthongensis sp. n. (6 in Fig. 1) E Khammouane, one of the main entrances of Tham Pha Soung Cave F Tham Pha Soung Cave, sampling at Frog Lake (4 in Fig. 1). (Photos: Ondrej Kameniar, Mário Olšavský and Jozef Grego).

Figure 3 from: de Oliveira Dias C, de Araujo AV, Bonecker SLC (2018) Vertical distribution and structure of copepod (Arthropoda: Copepoda) assemblages in two different seasons down to 1,200 m in the tropical Southwestern Atlantic. Zoologia 35: 1-11. https://doi.org/10.3897/zoologia.35.e13886

Figure 3 Vertical distribution of the mean and standard deviation of the copepod density (log ind.m-³) during two sampling periods: rainy season, RS; dry season, DS.

Figure 5 from: de Oliveira Dias C, de Araujo AV, Bonecker SLC (2018) Vertical distribution and structure of copepod (Arthropoda: Copepoda) assemblages in two different seasons down to 1,200 m in the tropical Southwestern Atlantic. Zoologia 35: 1-11. https://doi.org/10.3897/zoologia.35.e13886

Figure 5 DbRDA ordination derived from DistLM analysis, including the main environmental parameters explaining the variability in copepod assemblage structures during the sampling period. Temp, temperature; Sal, salinity. Black triangle, rainy season 1 m; open triangle, dry season 1 m; black circle, rainy season 250 m; open circle, dry season 250 m; black square, rainy season 800 m; open square, dry season 800 m; black polygon, rainy season 1,200 m; open polygon, dry season 1,200 m.

Figure 1 from: de Oliveira Dias C, de Araujo AV, Bonecker SLC (2018) Vertical distribution and structure of copepod (Arthropoda: Copepoda) assemblages in two different seasons down to 1,200 m in the tropical Southwestern Atlantic. Zoologia 35: 1-11. https://doi.org/10.3897/zoologia.35.e13886

Figure 1 Salinity and temperature of the five water masses (0–3260 m) in the Campos Basin, central Brazilian coast, modified from Bonecker et al. (2014). Solid line = temperature; dashed line = salinity; SS, Subsurface Water; SACW, South Atlantic Central Water; AAIW, Antarctic Intermediate Water; UCDW, Upper Circumpolar Deep Water; NADW, North Atlantic Deep Water.

Figure 4 from: de Oliveira Dias C, de Araujo AV, Bonecker SLC (2018) Vertical distribution and structure of copepod (Arthropoda: Copepoda) assemblages in two different seasons down to 1,200 m in the tropical Southwestern Atlantic. Zoologia 35: 1-11. https://doi.org/10.3897/zoologia.35.e13886

Figure 4 Vertical distribution of the mean diversity, species richness, and evenness of total copepods in the Campos Basin: dark blue bars, diversity; cobalt bars, richness; cyan bar, evenness. RS, rainy season; DS, dry season.

Fig 4 from: Kenyeres Z (2018) Effects of grazing on orthopteran assemblages of Central-European sand grasslands. Journal of Orthoptera Research 27(1): 23-33. https://doi.org/10.3897/jor.27.15033

Fig 4 Mean values (min-max and ±SE) of species number and frequency of habitat specialist species under different grazing pressure. Significant (p<0.05) differences detected by Mann-Whitney U test are indicated by different letters.

Fig 2 from: Kenyeres Z (2018) Effects of grazing on orthopteran assemblages of Central-European sand grasslands. Journal of Orthoptera Research 27(1): 23-33. https://doi.org/10.3897/jor.27.15033

Fig 2 Mean values (min-max and ±SE) of main parameters of orthopteran assemblages under different grazing pressure. Significant (p<0.05) differences detected by Mann-Whitney U test are indicated by different letters.

Fig 1 from: Kenyeres Z (2018) Effects of grazing on orthopteran assemblages of Central-European sand grasslands. Journal of Orthoptera Research 27(1): 23-33. https://doi.org/10.3897/jor.27.15033

Fig 1 Location and land use-changes of the studied sites (G: grazed; G–A: grazing-abandoned; M–G: moderately grazed; U–G: ungrazed). Letters to the left of the arrow indicate land use in 2012 and 2013; letters to the right of the arrow indicate land use in 2014, 2015 and 2016.

Fig 5 from: Kenyeres Z (2018) Effects of grazing on orthopteran assemblages of Central-European sand grasslands. Journal of Orthoptera Research 27(1): 23-33. https://doi.org/10.3897/jor.27.15033

Fig 5 Mean values (min-max and ±SE) of relative frequency of geophilic and vegetation structure-dependent species under different grazing pressure. Significant (p<0.05) differences detected by Mann-Whitney U test are indicated by different letters.

Fig 3 from: Kenyeres Z (2018) Effects of grazing on orthopteran assemblages of Central-European sand grasslands. Journal of Orthoptera Research 27(1): 23-33. https://doi.org/10.3897/jor.27.15033

Fig 3 PCoA ordination (sum of all eigenvalues: 20.008, similarity index: correlation) based on Orthoptera data. The different years are marked by A, B, C, D and E (A: 2012, B: 2013, C: 2014, D: 2015 and E: 2016; e.g. 1-A: site 1 in 2012, 2-B: site 2 in 2013, C-C: control site in 2014).

Fig 7 from: Kenyeres Z (2018) Effects of grazing on orthopteran assemblages of Central-European sand grasslands. Journal of Orthoptera Research 27(1): 23-33. https://doi.org/10.3897/jor.27.15033

Fig 7 CCA ordination based on Orthoptera data and environmental parameters (VCOV: total vegetation cover; BSOIL: percentage of bare soil; VH: height of the vegetation). Abbreviations of species names: Acr ins: Acrotylus insubricus; Acr ung: Acrida ungarica; Ail tha: Aiolopus thalassinus; Cal bar: Calliptamus barbarus; Cal ita: Calliptamus italicus; Cel var: Celes variabilis; Cho apr: Chorthippus apricarius; Cho big: Chorthippus biguttulus; Cho bru: Chorthippus brunneus; Cho mol: Chorthippus mollis; Doc bre: Dociostaurus brevicollis; Euc dec: Euchorthippus declivus; Euc pul: Euchorthippus pulvinatus; Gam gla: Gampsocleis glabra; Mon mon: Montana montana; Myr mac: Myrmeleotettix maculatus; Oed cae: Oedipoda caerulescens; Oed dec: Oedaleus decorus; Omo hae: Omocestus haemorrhoidalis; Omo min: Omocestus minutus; Omo pet: Omocestus petraeus; Omo ruf: Omocestus rufipes; Pla alb: Platycleis albopunctata; Sph cae: Sphingonotus caerulans; Ste fis: Stenobothrus fischeri; Ste lin: Stenobothrus lineatus; Ste nig: Stenobothrus nigromaculatus.

Fig 6 from: Kenyeres Z (2018) Effects of grazing on orthopteran assemblages of Central-European sand grasslands. Journal of Orthoptera Research 27(1): 23-33. https://doi.org/10.3897/jor.27.15033

Fig 6 Mean values (min-max and ±SE) of vegetation cover and vegetation height on the studied sites. Significant (p<0.05) differences detected by Mann-Whitney U test are indicated by different letters.

Figure 5 from: Sampaio ILR, Santos CP, França RC, Pedrosa IMMC, Solé M, França FGR (2018) Ecological diversity of a snake assemblage from the Atlantic Forest at the south coast of Paraíba, northeast Brazil. ZooKeys 787: 107-125. https://doi.org/10.3897/zookeys.787.26946

Figure 5 Species from the Atlantic Forest in south coast of Paraíba: APhilodryaspatagoniensisBPhimophisgueriniCSibonnebulatusDSibynomorphusmikaniiETaeniophallusoccipitalisFXenodonmerremiiGMicrurusibibobocaHMicruruspotyguaraIEpictiaborapeliotesJAmerotyphlopsbrongersmianusKBothropsleucurusLCrotalusdurissus. Photograph credits: Ivan L. Sampaio (A, B, D, E, H, I), Frederico G. França (F, G, J, L), Pedro T. S. Moura (C) Rafaela C. França (K).

Figure 3 from: Sampaio ILR, Santos CP, França RC, Pedrosa IMMC, Solé M, França FGR (2018) Ecological diversity of a snake assemblage from the Atlantic Forest at the south coast of Paraíba, northeast Brazil. ZooKeys 787: 107-125. https://doi.org/10.3897/zookeys.787.26946

Figure 3 Phytophisiognomies of Atlantic Forest in south coast of Paraíba. A Forest B Restinga C Savanna enclave (Tabuleiro). Photograph credits: Ivan L. Sampaio (A, B), Frederico G. França (C).

Figure 2 from: Sampaio ILR, Santos CP, França RC, Pedrosa IMMC, Solé M, França FGR (2018) Ecological diversity of a snake assemblage from the Atlantic Forest at the south coast of Paraíba, northeast Brazil. ZooKeys 787: 107-125. https://doi.org/10.3897/zookeys.787.26946

Figure 2 Variation of temperature, maximum (line with square) and minimum (line with triangle), precipitation as bars. Data from January 2012 and December 2013 (Source: INMET, http://www.inmet.gov.br/portal/index.php?r=bdmep/bdmep).

Figure 1 from: Sampaio ILR, Santos CP, França RC, Pedrosa IMMC, Solé M, França FGR (2018) Ecological diversity of a snake assemblage from the Atlantic Forest at the south coast of Paraíba, northeast Brazil. ZooKeys 787: 107-125. https://doi.org/10.3897/zookeys.787.26946

Figure 1 Schematic map showing the south coast of Paraíba state. Detail box: Barra de Gramame, located in the municipality of João Pessoa. The numbers represent the following municipalities: 1 João Pessoa 2 Conde 3 Alhandra 4 Pitimbu 5 Caaporã and 6 Pedras de Fogo.