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Figure 1 from: Cabral TS, Silva BDB, Martín MP, Clement CR, Hosaka K, Baseia IG (2019) Behind the veil – exploring the diversity in Phallus indusiatus s.l. (Phallomycetidae, Basidiomycota). MycoKeys 58: 103-127. https://doi.org/10.3897/mycokeys.58.35324

Figure 1 Currently known distributions of the Phallus species described in this study. Highlighted areas are the Brazilian Biomes (IBGE 2012): Amazonian Rainforest, Cerrado, Caatinga, Atlantic Rainforest, Pantanal and Pampa.

Figure 2 from: Cabral TS, Silva BDB, Martín MP, Clement CR, Hosaka K, Baseia IG (2019) Behind the veil – exploring the diversity in Phallus indusiatus s.l. (Phallomycetidae, Basidiomycota). MycoKeys 58: 103-127. https://doi.org/10.3897/mycokeys.58.35324

Figure 2 Phylogenetic tree obtained by Bayesian analysis with ITS. Brazilian clades corresponding to the new species and P. indusiatus are indicated (the holotype of each species is in bold). Posterior probabilities and bootstrap values are on the nodes (pp/bs), values of pp < 0.95 and bs < 90 are not shown. The black dots indicate specimens under Phallus indusiatus deposited in GenBank and downloaded for this study.

Figure 3 from: Cabral TS, Silva BDB, Martín MP, Clement CR, Hosaka K, Baseia IG (2019) Behind the veil – exploring the diversity in Phallus indusiatus s.l. (Phallomycetidae, Basidiomycota). MycoKeys 58: 103-127. https://doi.org/10.3897/mycokeys.58.35324

Figure 3 Phylogenetic tree obtained by Bayesian analysis with concatenated data (ITS, nuc-LSU and atp6). Brazilian clades corresponding to the new species and P. indusiatus are indicated (the holotype of each species is in bold). Posterior probabilities and bootstrap values are on the nodes (pp/bs), values of pp < 0.95 and bs < 90 are not shown (except for P. denigricans clade).

Figure 7 from: Cabral TS, Silva BDB, Martín MP, Clement CR, Hosaka K, Baseia IG (2019) Behind the veil – exploring the diversity in Phallus indusiatus s.l. (Phallomycetidae, Basidiomycota). MycoKeys 58: 103-127. https://doi.org/10.3897/mycokeys.58.35324

Figure 7 Phallus indusiatus. Fresh basidiome of A INPA-Fungos 264931 (neotype), and B INPA-Fungos 264929, showing the volva with pinkish pigments C spores D pseudoparenchymatous hyphae from pseudostipe E hyphae from volva and crystals deposits on globose cells F hyphae from rhizomorphs. Scale bars: 20 mm (A, B); 10 µm (C); 40 µm (D); 20 µm (E, F).

Figure 4 from: Cabral TS, Silva BDB, Martín MP, Clement CR, Hosaka K, Baseia IG (2019) Behind the veil – exploring the diversity in Phallus indusiatus s.l. (Phallomycetidae, Basidiomycota). MycoKeys 58: 103-127. https://doi.org/10.3897/mycokeys.58.35324

Figure 4 Phallus denigricans UFRN-Fungos 2805, holotype. A Basidiome B blackish and smooth volva in detail C white volva with projections D receptacle with a prominent pore E spores F pseudoparenchymatous hyphae of pseudostipe G hyphae from rhizomorphs H hyphae from volva. Scale bars: 20 mm (A–D), 20 µm (E), 40 µm (F–H).

Figure 6 from: Cabral TS, Silva BDB, Martín MP, Clement CR, Hosaka K, Baseia IG (2019) Behind the veil – exploring the diversity in Phallus indusiatus s.l. (Phallomycetidae, Basidiomycota). MycoKeys 58: 103-127. https://doi.org/10.3897/mycokeys.58.35324

Figure 6 Phallus squamulosus UFRN-Fungos 2806, holotype. A Fresh basidiome B immature basidiome with squamous surface C spores D pseudoparenchymatous hyphae from pseudostipe E hyphae from volva F hyphae from rhizomorphs and crystals deposits on globose cells. Scale bars: 20 mm (A, B), 20 µm (C–F).

Figure 5 from: Cabral TS, Silva BDB, Martín MP, Clement CR, Hosaka K, Baseia IG (2019) Behind the veil – exploring the diversity in Phallus indusiatus s.l. (Phallomycetidae, Basidiomycota). MycoKeys 58: 103-127. https://doi.org/10.3897/mycokeys.58.35324

Figure 5 Phallus purpurascens SINOP27, paratype. A Fresh basidiome B gregarious immature basidiome, with purplish pigments on surface C longitudinal section of an immature basidiome, showing the purplish volva and rhizomorphs. Phallus purpurascens UFRN-Fungos 2808, holotype. D Spores E rhizomorphs hyphae F pseudoparenchymatous hyphae from pseudostipe G hyphae from volva H crystals in globose cells found on volva. Scale bars: 20 mm (A–C), 20 µm (C–H).

Supplementary material 3 from: Amador-Castro IG, Fernández-Rivera Melo FJ, Torre J (2021) Marine diversity in the biosphere reserve of the most oceanic island in the Gulf of California: San Pedro Mártir. ZooKeys 1062: 177-201. https://doi.org/10.3897/zookeys.1062.67964

Table S3

Supplementary material 1 from: Amador-Castro IG, Fernández-Rivera Melo FJ, Torre J (2021) Marine diversity in the biosphere reserve of the most oceanic island in the Gulf of California: San Pedro Mártir. ZooKeys 1062: 177-201. https://doi.org/10.3897/zookeys.1062.67964

Table S1

Supplementary material 4 from: Amador-Castro IG, Fernández-Rivera Melo FJ, Torre J (2021) Marine diversity in the biosphere reserve of the most oceanic island in the Gulf of California: San Pedro Mártir. ZooKeys 1062: 177-201. https://doi.org/10.3897/zookeys.1062.67964

Table S4

Supplementary material 2 from: Amador-Castro IG, Fernández-Rivera Melo FJ, Torre J (2021) Marine diversity in the biosphere reserve of the most oceanic island in the Gulf of California: San Pedro Mártir. ZooKeys 1062: 177-201. https://doi.org/10.3897/zookeys.1062.67964

Table S2

Figure 4 from: Amador-Castro IG, Fernández-Rivera Melo FJ, Torre J (2021) Marine diversity in the biosphere reserve of the most oceanic island in the Gulf of California: San Pedro Mártir. ZooKeys 1062: 177-201. https://doi.org/10.3897/zookeys.1062.67964

Figure 4 Ecological indicators of fish species richness (S), Shannon-Wiener diversity (H'), and Pielou evenness (J') by transect. The inferior and superior sides of each blue rectangle represent the first and third quartiles (P25 and P75), respectively, and the median is represented by the horizontal black line. The points indicate the values of each data point, while the line surrounding each box plot shows the probability density.

Figure 3 from: Amador-Castro IG, Fernández-Rivera Melo FJ, Torre J (2021) Marine diversity in the biosphere reserve of the most oceanic island in the Gulf of California: San Pedro Mártir. ZooKeys 1062: 177-201. https://doi.org/10.3897/zookeys.1062.67964

Figure 3 Ecological indicators of invertebrate species richness (S), Shannon-Wiener diversity (H'), and Pielou evenness (J') by transect. The inferior and superior sides of each blue rectangle represent the first and third quartiles (P25 and P75), respectively, and the median is represented by the horizontal black line. The points indicate the values of each data point, while the line surrounding each box plot shows the probability density.

Figure 2 from: Amador-Castro IG, Fernández-Rivera Melo FJ, Torre J (2021) Marine diversity in the biosphere reserve of the most oceanic island in the Gulf of California: San Pedro Mártir. ZooKeys 1062: 177-201. https://doi.org/10.3897/zookeys.1062.67964

Figure 2 Total abundance and number of a invertebrate and b fish species observed per year in the Island San Pedro Mártir Biosphere Reserve (ISPMBR) in the Gulf of California, Mexico.

Figure 1 from: Amador-Castro IG, Fernández-Rivera Melo FJ, Torre J (2021) Marine diversity in the biosphere reserve of the most oceanic island in the Gulf of California: San Pedro Mártir. ZooKeys 1062: 177-201. https://doi.org/10.3897/zookeys.1062.67964

Figure 1 Left panel: Map of the Gulf of California and surrounding areas. The Midriff Islands region (MIR, dotted line) includes the a Bahía de los Ángeles, Canales de Ballenas y Salsipuedes Biosphere Reserve; b Archipiélago de San Lorenzo National Park; and c island San Pedro Mártir Biosphere Reserve (ISPMBR), whereas d Bahía de Loreto National Park is located to the south of the MIR. Right panel: The limits of the ISPMBR, including Island San Pedro Mártir (shaded region) and the monitoring sites (1–6) of this study. 1 Punta Rabijunco 2 Cueva de la Reserva and 3 Los Morritos are located within the core, no-take zone (dashed region) of the ISPMBR, whereas 4 Cueva del Biólogo 5 Barra Baya 6 La Ventana and 7 Arroyo del Cartelón are located within the buffer zone.

Figure 5 from: Lee G-E, Han T, Jeong J, Kim S-H, Park IG, Park H (2015) Molecular phylogeny of the genus Dicronocephalus (Coleoptera, Scarabaeidae, Cetoniinae) based on mtCOI and 16S rRNA genes. ZooKeys 501: 63-87. https://doi.org/10.3897/zookeys.501.8658

Figure 5 - Anterior edge of clypeus of Dicronocephalus. A Dicronocephalus adamsi adamsi B Dicronocephalus adamsi drumonti C Dicranocephalus yui yui D Dicronocephalus dabryi E Dicronocephalus uenoi katoi F Dicronocephalus wallichii bowringi G Dicronocephalus wallichii wallichii H Dicronocephalus wallichii bourgoini.

Figure 4 from: Lee G-E, Han T, Jeong J, Kim S-H, Park IG, Park H (2015) Molecular phylogeny of the genus Dicronocephalus (Coleoptera, Scarabaeidae, Cetoniinae) based on mtCOI and 16S rRNA genes. ZooKeys 501: 63-87. https://doi.org/10.3897/zookeys.501.8658

Figure 4 - Phylogenetic relationships among Dicronocephalus species reconstructed with Bayesian inference using COI and 16S rRNA sequences. Numbers above branches indicate ML bootstrap values and Bayesian posterior probabilities. Numbers below branches are bootstrap, symmetric resampling, and jacknife support from parsimony searches, respectively. Scale bar represents 10% nucleotide mutation rate.

Figure 1 from: Lee G-E, Han T, Jeong J, Kim S-H, Park IG, Park H (2015) Molecular phylogeny of the genus Dicronocephalus (Coleoptera, Scarabaeidae, Cetoniinae) based on mtCOI and 16S rRNA genes. ZooKeys 501: 63-87. https://doi.org/10.3897/zookeys.501.8658

Figure 1 - The male habitus of species and subspecies of Dicoronocephalus. A Dicronocephalus adamsi adamsi B Dicronocephalus adamsi drumonti C Dicranocephalus yui yui D Dicronocephalus dabryi E Dicronocephalus uenoi katoi F Dicronocephalus wallichii bowringi G Dicronocephalus wallichii wallichii H Dicronocephalus wallichii bourgoini.

Figure 8 from: Lee G-E, Han T, Jeong J, Kim S-H, Park IG, Park H (2015) Molecular phylogeny of the genus Dicronocephalus (Coleoptera, Scarabaeidae, Cetoniinae) based on mtCOI and 16S rRNA genes. ZooKeys 501: 63-87. https://doi.org/10.3897/zookeys.501.8658

Figure 8 - Metasternal process (in the circle) and aedeagi of Dicronocephalus adamsi drumonti and Dicronocephalus adamsi adamsi. A, B, C, D Dicronocephalus adamsi drumonti (Tibet) E, F, G, H Dicronocephalus adamsi drumonti (Sichuan) I, J, K, L Dicronocephalus adamsi adamsi (South Korea) M, N, O, P Dicronocephalus adamsi adamsi (North Korea) Q, R, S, T Dicronocephalus adamsi adamsi (Dandong, China).

Figure 3 from: Lee G-E, Han T, Jeong J, Kim S-H, Park IG, Park H (2015) Molecular phylogeny of the genus Dicronocephalus (Coleoptera, Scarabaeidae, Cetoniinae) based on mtCOI and 16S rRNA genes. ZooKeys 501: 63-87. https://doi.org/10.3897/zookeys.501.8658

Figure 3 - Phylogenetic relationships among Dicronocephalus species reconstructed with Bayesian inference using 16S rRNA sequences. Numbers above branches indicate ML bootstrap values and Bayesian posterior probabilities. Numbers below branches are bootstrap, symmetric resampling, and jacknife support from parsimony searches, respectively. Scale bar represents 10% nucleotide mutation rate.