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FIGURE 3 in Under the surface: what we know about the threats to subterranean fishes in Brazil

FIGURE 3 | Detailed maps showing the distribution of Brazilian subterranean fishes in different federated states, including vegetation and impacts nearby. AP, Amapá State; PA, Pará State; RO, Rondônia State; MS, Mato Grosso do Sul State; BA, Bahia State; SP, São Paulo State, MG, Minas Gerais State; GO, Goiás State. Outcrops, landscape areas with rocks and potentially cave occurrences.

FIGURE 6 in Under the surface: what we know about the threats to subterranean fishes in Brazil

FIGURE 6 | Total number of Brazilian subterranean fish species affected by each type of identified threat in the present study.

FIGURE 1 in Under the surface: what we know about the threats to subterranean fishes in Brazil

FIGURE 1 | Map of Brazil showing the distribution of the subterranean fish species according to the basins included in the country's territory.

FIGURE 5 in Under the surface: what we know about the threats to subterranean fishes in Brazil

FIGURE 5 | A. Ituglanis epikarsticus from the Lapa do São Mateus cave, São Domingos, Goiás State, live specimen, 28 mm SL; Photo: Adriano Gambarini. B. Rhamdiopsis sp. "caatinga", live specimen, 59 mm SL; Photo: Jonas Eduardo Gallão. C. Stygichthys typhlops from the Jaíba region, Minas Gerais State, live specimen, 25 mm SL, specimen captured in July 2008; Photo: Adriano Gambarini. All specimens were photographed in an aquarium at Laboratório de Estudos Subterrâneos, Universidade Federal de São Carlos.

opencc-by-4.0Apr 2020View details →

Fig. 2 in Erratum to Huang SB, Tian MY & Faille A (2020) Two new species of subterranean ground beetles from China (Coleoptera: Carabidae: Trechinae)

Fig. 2. Shilinotrechus anthonyi, new species, male genitalia. A, median lobe and parameres, lateral view; B, apical lobe, dorsal view.

TABLE 2 in Under the surface: what we know about the threats to subterranean fishes in Brazil

TABLE 2 | Brazilian subterranean fishes: threats, possible causes, IUCN categories, and occurrence in Conservation Units.<table><tbody><tr><th>Species</th><th>Threats</th><th>Possible causes</th><th>IUCN Brazilian Red List (ICMBio/MMA, 2018)</th><th>IUCN Global Red List</th><th>Conservation Unit</th></tr></tbody><tbody><tr><th>Stygichthys typhlops Brittan & Böhlke, 1965</th><td>Lowering of the aquifer; physical change of the habitat</td><td>Artesian wells for fruit irrigation; climate change</td><td>Endangered (EN)</td><td>Deficient Data (DD)</td><td>Not included</td></tr><tr><th>Eigenmannia vicentespelaea Triques, 1996</th><td>Lowering of the base-level stream; siltation of the subterranean drainage; tourism</td><td>Large scale agriculture and irrigation projects (in the headwaters); deforestation of headwaters; unmanaged tourism; climate change</td><td>Vulnerable (VU)</td><td>Not included</td><td>Terra Ronca State Park</td></tr><tr><th>Ancistrus cryptophthalmus Reis, 1987</th><td>Lowering of the base-level streams; tourism</td><td>Large scale agriculture and irrigation projects (in the headwaters); deforestation of the headwaters; unmanaged tourism; climate change</td><td>Endangered (EN)</td><td>Not included</td><td>Terra Ronca State Park</td></tr><tr><th>Ancistrus formoso Sabino & Trajano, 1997</th><td>Pollution; physical change of the habitat</td><td>Use of pesticides for agriculture; mining for cement production</td><td>Vulnerable (VU)</td><td>Not included</td><td>Limits of the Serra da Bodoquena National Park</td></tr><tr><th>Ancistrus sp. “bodoquena”</th><td>physical change of the habitat</td><td>Deforestation; mining projects for cement production</td><td>Not included</td><td>Not included</td><td>Not included</td></tr><tr><th>Aspidoras mephisto Tencatt & Bichuette, 2017</th><td>Pollution; physical change of the habitat; food restriction</td><td>Use of pesticides for agriculture; discharge of domestic sewage; mining projects for cement production; deforestation of cave surroundings</td><td>Not included</td><td>Not included</td><td>Not included</td></tr><tr><th>Trichomycterus itacarambiensis de Pinna & Trajano, 1996</th><td>Physical change of the habitat; food restriction</td><td>Dams inside the cave for water exploration; climate change</td><td>Critically Endangered (CR)</td><td>Not included</td><td>Limits of the Cavernas do Peruaçu National Park</td></tr><tr><th>Trichomycterus dali Rizzato, Costa-Jr, Trajano & Bichuette, 2011</th><td>Physical change of the habitat; pollution</td><td>Mining projects for cement production; water exploration (irrigation for agriculture); deforestation of caves surroundings (agriculture and pastures); climate change</td><td>Vulnerable (VU)</td><td>Not included</td><td>Limits of the Serra da Bodoquena National Park (part)</td></tr><tr><th>Trichomycterus rubbioli Bichuette & Rizzato, 2012</th><td>Food restriction; physical change of the habitat; lowering of the upper phreatic</td><td>Deforestation of cave surroundings (agriculture; pastures and charcoal production); potential large scale mining projects; climate change</td><td>Vulnerable (VU)</td><td>Not included</td><td>Not included</td></tr><tr><th>Trichomycterus sp. “ramalho”</th><td>Lowering of the base-level stream; food restriction</td><td>Deforestation of cave surroundings (pastures and charcoal production); climate change</td><td>Not included</td><td>Not included</td><td>Not included</td></tr><tr><th>Trichomycterus sp. “iu iu”</th><td>Lowering of the base-level stream; food restriction</td><td>Deforestation for agriculture and pastures (small scale); climate change</td><td>Not included</td><td>Not included</td><td>Not included</td></tr><tr><th>Ituglanis passensis Fernández & Bichuette, 2002</th><td>Lowering of the base-level stream; siltation of subterranean drainage; food restriction</td><td>Deforestation for agriculture and pastures (small scale); climate change</td><td>Vulnerable (VU)</td><td>Not included</td><td>Terra Ronca State Park</td></tr><tr><th>Ituglanis bambui Bichuette & Trajano, 2004</th><td>Siltation of the upper vadose tributary; lowering of the upper vadose tributary; tourism</td><td>Unmanaged tourism; climate change</td><td>Critically Endangered (CR)</td><td>Not included</td><td>Terra Ronca State Park</td></tr><tr><th>Ituglanis epikarsticus Bichuette & Trajano, 2004</th><td>Lowering of the epikarst (upper aquifer); physical change of the habitat; tourism</td><td>Climate change; unmanaged tourism</td><td>Vulnerable (VU)</td><td>Not included</td><td>Terra Ronca State Park</td></tr><tr><th>Ituglanis ramiroi Bichuette & Trajano, 2004</th><td>Lowering of the upper vadose tributary; physical change of the habitat; tourism</td><td>Climate change; unmanaged tourism</td><td>Vulnerable (VU)</td><td>Not included</td><td>Terra Ronca State Park</td></tr><tr><th>Ituglanis mambai Bichuette & Trajano, 2008</th><td>Food restriction; siltation of the subterranean drainage</td><td>Deforestation of surroundings (agriculture and pastures)</td><td>Endangered (EN)</td><td>Not included</td><td>Not included</td></tr><tr><th>Ituglanis boticario Rizzato & Bichuette, 2015</th><td>Food restriction; siltation of the subterranean drainage</td><td>Deforestation of surroundings (agriculture and pastures)</td><td>Not included</td><td>Not included</td><td>Rio Vermelho Environmental Protection Area (APA)</td></tr><tr><th>Ituglanis sp. “terra ronca”</th><td>No data</td><td>No data</td><td>Not included</td><td>Not included</td><td>Terra Ronca State Park</td></tr><tr><th>Ituglanis sp. “posse”</th><td>Physical change of the habitat; lowering of the upper phreatic</td><td>Dams inside the cave for water exploration; climate change</td><td>Not included</td><td>Not included</td><td>Not included</td></tr><tr><th>Ituglanis sp. “canastra”</th><td>Food restriction; lowering of the base-level stream</td><td>Deforestation of surroundings; climate change</td><td>Not included</td><td>Not included</td><td>Limits of the Serra da Canastra National Park</td></tr><tr><th>Glaphyropoma spinosum Bichuette, de Pinna & Trajano, 2008</th><td>Physical change of the habitat; tourism</td><td>Illegal gold panning (“garimpo”); unmanaged tourism</td><td>Vulnerable (VU)</td><td>Not included</td><td>Chapada Diamantina National Park</td></tr><tr><th>Copionodon sp. “igatu”</th><td>Physical change of the habitat; tourism</td><td>Illegal gold panning (“garimpo”); unmanaged tourism</td><td>Not included</td><td>Not included</td><td>Chapada Diamantina National Park</td></tr><tr><th>Pimelodella kronei (Miranda Ribeiro, 1907)</th><td>Pollution (domestic sewage and others); overcollecting; physical change of the habitat</td><td>Irregular land use; weak supervising; irregular visitation of the cave</td><td>Endangered (EN)</td><td>Deficient Data (DD)</td><td>TurÍstico do Alto Ribeira State Park</td></tr><tr><th>Pimelodella spelaea Trajano, Reis & Bichuette, 2007</th><td>Lowering of the upper vadose tributary; physical change of the habitat; tourism</td><td>Climate change; unmanaged tourism</td><td>Endangered (EN)</td><td>Not included</td><td>Terra Ronca State Park</td></tr><tr><th>Pimelodella sp. “açungui”</th><td>Physical change of the habitat</td><td>Small Hydroelectric Power Station (SHPS)</td><td>Not included</td><td>Not included</td><td>Not included</td></tr><tr><th>Rhamdia enfurnada Bichuette & Trajano, 2005</th><td>Food restriction; physical change of the habitat; lowering of the base-level stream</td><td>Deforestation of cave surroundings (agriculture; pastures and charcoal production); potential large scale mining projects; climate change</td><td>Not included</td><td>Not included</td><td>Not included</td></tr><tr><th>Rhamdia sp. “bodoquena”</th><td>Physical alteration of the habitat</td><td>Deforestation of cave surroundings; mining projects for cement production</td><td>Not included</td><td>Not included</td><td>Not included</td></tr><tr><th>Rhamdiopsis krugi Bockmann & Castro, 2010</th><td>Siltation; food restriction; lowering of the aquifer; pollution (part of the aquifer); tourism (part of the caves)</td><td>Deforestation of caves surroundings; installation of artesian wells; use of pesticides for agriculture; unmanaged tourism</td><td>Vulnerable (VU)</td><td>Not included</td><td>Not included</td></tr><tr><th>Rhamdiopsis sp. “gonçalo”</th><td>Lowering of the aquifer; physical change of the habitat</td><td>Water withdrawal and installation of artesian wells for human consumption and agriculture use (small scale); old saltpeter exploration</td><td>Not included</td><td>Not included</td><td>Not included</td></tr><tr><th>Rhamdiopsis sp. “cordisburgo”</th><td>No data</td><td>No data</td><td>Not included</td><td>Not included</td><td>Not included</td></tr><tr><th>Rhamdiopsis sp. “ramalho”, two populations/ morphotypes</th><td>Lowering of the upper phreatic; physical change of the habitat</td><td>Water withdrawal for human consumption and agriculture (small scale); dams inside the caves</td><td>Not included</td><td>Not included</td><td>Not included</td></tr><tr><th>Rhamdiopsis sp. “caatinga”</th><td>Lowering of the aquifer; physical change of the habitat</td><td>Water withdrawal for human consumption and agriculture use (small scale); dams inside the cave</td><td>Not included</td><td>Not included</td><td>Not included</td></tr><tr><th>Phenacorhamdia sp. “posse”</th><td>Physical change of the habitat; lowering of the upper phreatic</td><td>Dams inside the cave; water withdrawal; climate change</td><td>Not included</td><td>Not included</td><td>Not included</td></tr><tr><th>Phreatobius cisternarum Goeldi, 1905</th><td>Habitat fragmentation; food restriction</td><td>Deforestation for agriculture and pasture activities</td><td>Least Concerned (LC)</td><td>Deficient Data (DD)</td><td>Not included</td></tr><tr><th>Phreatobius dracunculus Shibatta, Muriel-Cunha & de Pinna, 2007</th><td>Habitat fragmentation; food restriction</td><td>Deforestation for agriculture and pasture activities; mining</td><td>Deficient Data (DD)</td><td>Not included</td><td>Not included</td></tr><tr><th>Phreatobius sanguijuela Fernández, Saucedo, Carvajal-Vallejos & Schaefer, 2007</th><td>Habitat fragmentation; food restriction</td><td>Deforestation for agriculture and pasture activities</td><td>Not included</td><td>Critically Endangered (CR)</td><td>Not included</td></tr></tbody></table>

TABLE 1 in Under the surface: what we know about the threats to subterranean fishes in Brazil

TABLE 1 | List of the currently known Brazilian subterranean fishes species occurring in Brazil, their basins of occurrence, type of habitats / number of localities (caves or non-cave habitats). * Undescribed species with references.<table><tbody><tr><th>Species</th><th>River basin</th><th>State</th><th>Habitat / number of caves or localities</th></tr></tbody><tbody><tr><th>Stygichthys typhlops Brittan & Böhlke, 1965</th><td>Middle rio São Francisco</td><td>Minas Gerais</td><td>Phreatic / 1</td></tr><tr><th>Eigenmannia vicentespelaea Triques, 1996</th><td>Upper rio Tocantins</td><td>Goiás</td><td>Base-level stream / 2</td></tr><tr><th>Ancistrus cryptophthalmus Reis, 1987</th><td>Upper rio Tocantins</td><td>Goiás</td><td>Base-level stream / 4</td></tr><tr><th>Ancistrus formoso Sabino & Trajano, 1997</th><td>Upper rio Paraguai</td><td>Mato Grosso do Sul</td><td>Flooded caves / 3</td></tr><tr><th>Ancistrus sp. “Bodoquena”* (Trajano, Bichuette, 2010; Borghezan, 2013)</th><td>Upper rio Paraguai</td><td>Mato Grosso do Sul</td><td>Flooded cave / 2</td></tr><tr><th>Aspidoras mephisto Tencatt & Bichuette, 2017</th><td>Upper rio Tocantins</td><td>Goiás</td><td>Base-level stream / 2</td></tr><tr><th>Trichomycterus itacarambiensis de Pinna & Trajano, 1996</th><td>Middle rio São Francisco</td><td>Minas Gerais</td><td>Base-level stream / 1</td></tr><tr><th>Trichomycterus dali Rizzato, Costa-Jr, Trajano & Bichuette, 2011</th><td>Upper rio Paraguai</td><td>Mato Grosso do Sul</td><td>Flooded caves / 3</td></tr><tr><th>Trichomycterus rubbioli Bichuette & Rizzato, 2012</th><td>Middle rio São Francisco</td><td>Bahia</td><td>Upper Phreatic (cave) /1</td></tr><tr><th>Trichomycterus sp. “ramalho”* (Bichuette, 2021)</th><td>Middle rio São Francisco</td><td>Bahia</td><td>Base-level stream / 1</td></tr><tr><th>Trichomycterus sp. “iu iu”* (Bichuette, 2021)</th><td>Middle rio São Francisco</td><td>Bahia</td><td>Upper Phreatic (cave) / 1</td></tr><tr><th>Ituglanis passensis Fernández & Bichuette, 2002</th><td>Upper rio Tocantins</td><td>Goiás</td><td>Base-level stream / 1</td></tr><tr><th>Ituglanis bambui Bichuette & Trajano, 2004</th><td>Upper rio Tocantins</td><td>Goiás</td><td>Vadose tributary / 1</td></tr><tr><th>Ituglanis epikarsticus Bichuette & Trajano, 2004</th><td>Upper rio Tocantins</td><td>Goiás</td><td>Epikarst / 1</td></tr><tr><th>Ituglanis ramiroi Bichuette & Trajano, 2004</th><td>Upper rio Tocantins</td><td>Goiás</td><td>Vadose tributary /1</td></tr><tr><th>Ituglanis mambai Bichuette & Trajano, 2008</th><td>Upper rio Tocantins</td><td>Goiás</td><td>Base-level stream / 1</td></tr><tr><th>Ituglanis boticario Rizzato & Bichuette, 2015</th><td>Upper rio Tocantins</td><td>Goiás</td><td>Base-level stream / 1</td></tr><tr><th>Ituglanis sp. “terra ronca”* (Bichuette, 2021)</th><td>Upper rio Tocantins</td><td>Goiás</td><td>Vadose tributary / 1</td></tr><tr><th>Ituglanis sp. “posse”* (Bichuette, 2021)</th><td>Upper rio Tocantins</td><td>Goiás</td><td>Upper Phreatic (cave) / 1</td></tr><tr><th>Ituglanis sp. “canastra”* (Bichuette, 2021)</th><td>Upper rio São Francisco</td><td>Minas Gerais</td><td>Base-level stream</td></tr><tr><th>Glaphyropoma spinosum Bichuette, de Pinna & Trajano, 2008</th><td>Upper rio Paraguaçu</td><td>Bahia</td><td>Base-level stream / 8</td></tr><tr><th>Copionodon sp. “igatu”* (Bichuette, 2021)</th><td>Upper rio Paraguaçu</td><td>Bahia</td><td>Base-level stream / 3</td></tr><tr><th>Pimelodella kronei (Miranda Ribeiro, 1907)</th><td>Upper rio Ribeira</td><td>São Paulo</td><td>Base-level stream / 7</td></tr><tr><th>Pimelodella spelaea Trajano, Reis & Bichuette, 2007</th><td>Upper rio Tocantins</td><td>Goiás</td><td>Vadose tributary / 1</td></tr><tr><th>Pimelodella sp. “açungui”* (Bichuette, 2021)</th><td>Upper rio Ribeira</td><td>São Paulo</td><td>Base-level stream / 1</td></tr><tr><th>Rhamdia enfurnada Bichuette & Trajano, 2005</th><td>Middle rio São Francisco</td><td>Bahia</td><td>Base-level stream / 1</td></tr><tr><th>Rhamdia sp. “Bodoquena”* (Trajano, Bichuette, 2010; Borghezan, 2013)</th><td>Upper rio Paraguai</td><td>Mato Grosso do Sul</td><td>Base-level stream / 2</td></tr><tr><th>Rhamdiopsis krugi Bockmann & Castro, 2010</th><td>Upper rio Paraguaçu</td><td>Bahia</td><td>Upper Phreatic (cave) / 12</td></tr><tr><th>Rhamdiopsis sp. “gonçalo”* (Trajano, Bichuette, 2010)</th><td>Middle rio São Francisco</td><td>Bahia</td><td>Upper Phreatic (cave) / 1</td></tr><tr><th>Rhamdiopsis sp. “cordisburgo”* (Trajano, Bichuette, 2010)</th><td>Middle rio São Francisco</td><td>Minas Gerais</td><td>Base-level stream / 1</td></tr><tr><th>Rhamdiopsis sp. “ramalho”*, two populations/ morphotypes (Bichuette, 2021)</th><td>Middle rio São Francisco</td><td>Bahia</td><td>Upper Phreatic (cave) / 1 and 1</td></tr><tr><th>Rhamdiopsis sp. “caatinga”* (Bichuette, 2021)</th><td>Middle rio São Francisco</td><td>Bahia</td><td>Upper Phreatic (cave) / 1</td></tr><tr><th>Phenacorhamdia sp. “posse”* (Bichuette, 2021)</th><td>Upper rio Tocantins</td><td>Goiás</td><td>Upper Phreatic (cave) / 1</td></tr><tr><th>Phreatobius cisternarum Goeldi, 1905</th><td>Amazon basin</td><td>Amapá; Pará</td><td>Hyporheic (alluvium) / 6</td></tr><tr><th>Phreatobius dracunculus Shibatta, Muriel-Cunha & de Pinna, 2007</th><td>Amazon basin</td><td>Rondônia</td><td>Hyporheic (alluvium) / 1</td></tr><tr><th>Phreatobius sanguijuela Fernández, Saucedo, Carvajal-Vallejos & Schaefer, 2007</th><td>Amazon basin</td><td>Rondônia</td><td>Hyporheic (alluvium) / 2</td></tr></tbody></table>

opencc-by-4.0Oct 2024View details →

Data for: Temporal consistency and spatial variability in detection: implications for monitoring of macroinvertebrates from shallow groundwater aquifers (Subterranean Biology, 2024)

Original research article: Knüsel M., Alther R., Couton M. & Altermatt F. (2024) Temporal consistency and spatial variability in detection: implications for monitoring of macroinvertebrates from shallow groundwater aquifers. Subterranean Biology 49: 139-161. <a href="https://doi.org/10.3897/subtbiol.49.132515" target="_blank" rel="noopener">https://doi.org/10.3897/subtbiol.49.132515</a>

opencc-zeroJan 2024View details →

Linked collectors and determiners for: Review of subterranean Quedius, with description of the first hypogean species from the Russian Far East (Coleoptera: Staphylinidae: Staphylinini).

Natural history specimen data linked to collectors and determiners held within, "Review of subterranean Quedius, with description of the first hypogean species from the Russian Far East (Coleoptera: Staphylinidae: Staphylinini)". Claims or attributions were made on Bionomia by volunteer Scribes, <a href="https://bionomia.net/dataset/e9fcf827-dcd7-4575-ae01-eee9465760f0">https://bionomia.net/dataset/e9fcf827-dcd7-4575-ae01-eee9465760f0</a> using specimen data from the dataset aggregated by the Global Biodiversity Information Facility, <a href="https://gbif.org/dataset/e9fcf827-dcd7-4575-ae01-eee9465760f0">https://gbif.org/dataset/e9fcf827-dcd7-4575-ae01-eee9465760f0</a>. Formatted as a Frictionless Data package.

opencc-zeroJan 2024View details →

Linked collectors and determiners for: A new subterranean Iberian Cephennium with unusually modified metatrochanters (Coleoptera, Staphylinidae, Scydmaeninae).

Natural history specimen data linked to collectors and determiners held within, "A new subterranean Iberian Cephennium with unusually modified metatrochanters (Coleoptera, Staphylinidae, Scydmaeninae)". Claims or attributions were made on Bionomia by volunteer Scribes, <a href="https://bionomia.net/dataset/229dc695-3b71-4365-bccf-16d4626c7b90">https://bionomia.net/dataset/229dc695-3b71-4365-bccf-16d4626c7b90</a> using specimen data from the dataset aggregated by the Global Biodiversity Information Facility, <a href="https://gbif.org/dataset/229dc695-3b71-4365-bccf-16d4626c7b90">https://gbif.org/dataset/229dc695-3b71-4365-bccf-16d4626c7b90</a>. Formatted as a Frictionless Data package.

opencc-by-4.0Apr 2007View details →

Figure 19. A in New gammaroid family, genera and species from subterranean waters of Japan, and their phylogenetic relationships (Crustacea: Amphipoda)

Figure 19. A, strict consensus tree obtained by maximum parsimony analysis; B, neighbour-joining tree. Numbers near branches indicate bootstrap values> 50%. Trees rooted by the outgroup taxon Melita sp.

Fig. 6 in Redescription of Formosan subterranean termite, Coptotermes formosanus (Blattodea: Rhinotermitidae), with three new synonyms from China

Fig. 6. The specimens of Coptotermes shanghaiensis Xia & He, 1986. a – winged imago; b – labels; c – forewing; d – hind wing.

Fig. 2 in Redescription of Formosan subterranean termite, Coptotermes formosanus (Blattodea: Rhinotermitidae), with three new synonyms from China

Fig. 2. Soldiers of Coptotermes formosanus Shiraki, 1909 from the same colony of the neotype. a – dorsal view of head; b – ventral view of head; c – dorsal view and lateral view of body; d – anterior view of fontanelle with four setae.

Fig. 1 in Redescription of Formosan subterranean termite, Coptotermes formosanus (Blattodea: Rhinotermitidae), with three new synonyms from China

Fig. 1. Neotype of Coptotermes formosanus Shiraki, 1909. a – dorsal view of body; b – anterior view of head; c – dorsal view of anterior body; d – hind wing; e – fore wing. The color of neotype became pale after preserving in ethanol for more than 10 years.

Fig. 5 in Redescription of Formosan subterranean termite, Coptotermes formosanus (Blattodea: Rhinotermitidae), with three new synonyms from China

Fig. 5. The type specimens of Coptotermes suzhouensis Xia & He, 1986. a – habitus of winged imago; b – imago in dorsal view; c – soldiers; d – labels.

Fig. 4 in Redescription of Formosan subterranean termite, Coptotermes formosanus (Blattodea: Rhinotermitidae), with three new synonyms from China

Fig. 4. The type specimens of Coptotermes changtaiensis Xia & He, 1986 and C. hekouensis Xia & He, 1986. a–b – C. changtaiensis: a – soldiers; b – labels. c–h – C. hekouensis: c – soldiers; d – labels; e–f – alate in dorsal view (e – pronotum facing up; f – head facing up); g – forewing; h – hind wing.

opencc-by-4.0Dec 2020View details →

Speciation of a subterranean amphipod on the southern margin of the Alpine ice-shield

Supplementary material comprising all the data used for the analyses in the "Speciation of a subterranean amphipod on the southern margin of the Alpine ice-shield " paper by Delić et al. 2021

opencc-by-4.0Nov 2019View details →

Figs 1–7 in A new subterranean Crematogaster with one ommatidium from Cambodia, based on morphology and DNA (Hymenoptera: Formicidae)

Figs 1–7. Crematogaster monocula sp. nov., holotype worker from Cambodia (HW 0.42; WL 0.53): 1 – body in lateral view; 2 – full-face view of head; 3 – dorsal view of mesosoma; 4 – lateral view of petiole and postpetiole; 5 – dorsal view of petiole and postpetiole; 6 – anterior view of mandible; 7 – lateral view of head. Scale bars = 0.2 mm.

opencc-by-4.0Jul 2017View details →

Map 1 in On Quedius coloratus FAUVEL, 1875 and allied species, with an appendix on Quedius species collected in Greece with subterranean pitfall traps, and a new synonymy (Coleoptera: Staphylinidae: Staphylininae)

Map 1: Distributions of Quedius hellenicus (black diamonds), Q. sp. 2 (white stars), Q. carpathius (black stars), Q. spiculatus (white triangles), Q. hebes (white circles), and Q. coloratus (black circles) in the East Mediterranean.