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FIGURE 3 in Population level genetic divergence and phylogenetic placement of Mexican shortfin mollies (Mollienesia: Poecilia: Poeciliidae)

FIGURE 3 | Cytochrome b (1,140 bp) mitochondrial gene Bayesian phylogeny, parsimony haplotype network, and sampling distribution of Poecilia sphenops (aqua-Atlantic North of the Trans Mexican Volcanic Belt, pink- Balsas River Drainage, purple- Atlantic North of the Isthmus of Tehuantepec, red- Pacific North of the Isthmus of Tehuantepec, orange- Atlantic South of the Isthmus of Tehuantepec, and yellow- Pacific South of the Trans Mexican Volcanic Belt) across geographic barriers along the coasts of Mexico. The phylogeny has Bayesian posterior values followed by bootstrap values with asterisks representing support of 95% or above. The Parsimony network values correspond to the haplotype values and are colored according by geographic locations separated by barriers; circle sizes correspond to the number of individuals with that haplotype (larger circles reflect more individuals), and black circles indicate unsampled haplotypes. The capital letters at the end of each sample represents the state of origin in Mexico, from North to South: V = Veracruz, H = Hidalgo, M = Michoacan, G = Guerrero, O = Oaxaca, C = Chiapas.

FIGURE 4 in Population level genetic divergence and phylogenetic placement of Mexican shortfin mollies (Mollienesia: Poecilia: Poeciliidae)

FIGURE 4 | Cytochrome b (1,140 bp) mitochondrial gene Bayesian phylogeny, parsimony haplotype network, and sampling distribution of the Pacific sister taxa Poecilia butleri (blue-North of the Trans Mexican Volcanic Belt) and P. nelsoni (lime green-South of the Trans Mexican Volcanic Belt, pink- Balsas River Drainage, red- North of the Isthmus of Tehuantepec, and yellow- South of the Trans Mexican Volcanic Belt) across geographic barriers along the coast of Mexico. The phylogeny has Bayesian posterior values followed by bootstrap values with asterisks representing support of 95% or above. The Parsimony network values correspond to the haplotype values and are colored according by geographic locations separated by barriers; circle sizes correspond to the number of individuals with that haplotype (larger circles reflect more individuals), and black cirles indicate unsampled haplotypes. The capital letters at the end of each sample represents the state of origin in Mexico, from North to South: S = Sinaloa, N = Nayarit, J = Jalisco, Cl = Colima, M = Michoacan, G = Guerrero, O = Oaxaca, C = Chiapas.

FIGURE 1 in Population level genetic divergence and phylogenetic placement of Mexican shortfin mollies (Mollienesia: Poecilia: Poeciliidae)

FIGURE 1 | Sampling localities of species in the subgenus Mollienesia in Mexico and the main physiographic barriers throughout the country. The main physiographic barriers in Mexico from north to south are Northwestern Plains and Sierras, Sierra Madre Occidental, Sierra Madre Oriental, Gulf Coast Plain, Trans Mexican Volcanic Belt, Balsas Depression, Sierra Madre del Sur, Isthmus of Tehuantepec, and Sierra Madre de Chiapas.

FIGURE 2 in Population level genetic divergence and phylogenetic placement of Mexican shortfin mollies (Mollienesia: Poecilia: Poeciliidae)

FIGURE 2 | Bayesian tree from the MrBayes partitioned analysis of Poecilia spp. for two mitochondrial genes (Cyt b and ND2, 2187 base pairs) and one nuclear (RAG1, 1561 base pairs) rooted with other poeciliid outgroups. Species names in black pertain to species outside of Mexico and species names in red are species found within Mexico. Species labels represent slope: (A) = Atlantic, (P) = Pacific, and (B) = Bi-coastal. Nodal support shown (left to right; respectively): Bayesian Posterior Probabilities followed by RAxML bootstrap support values. Asterisks denote nodal support of 95% or above for the two methods, and a single asterisk at a node indicates support values of 95% or above for both methods. Nodes with no values present either had low values or were of little interest for this study. The capital letters at the end of each sample represents the state of origin in Mexico, from North to South: T = Tamaulipas, NVL = Nuevo León, V = Veracruz, H = Hidalgo, M = Michoacan, G = Guerrero, O = Oaxaca, Tb = Tabasco, C = Chiapas.

FIGURE 1 in A new species of Knodus (Characiformes: Characidae), with deep genetic divergence, from the Mearim and Munim river basins, Northeastern Brazil, and evidence for hidden diversity in adjacent river basins

FIGURE 1 | Knodus guajajara, holotype, CICCAA 4883, 31.4 mm SL, Alto Alegre do Pindaré municipality, Igarapé Arapapá, Pindaré River drainage, Mearim River basin.

FIGURE 4 in A new species of Knodus (Characiformes: Characidae), with deep genetic divergence, from the Mearim and Munim river basins, Northeastern Brazil, and evidence for hidden diversity in adjacent river basins

FIGURE 4 | Knodus guajajara, CICCAA 4861, paratype, male, 31.9 mm SL Maranhão, Mearim River basin. A. Hooks on pelvic fin. B. Hooks on anal fin. (Photographed by F. P. Ottoni).

FIGURE 2 in A new species of Knodus (Characiformes: Characidae), with deep genetic divergence, from the Mearim and Munim river basins, Northeastern Brazil, and evidence for hidden diversity in adjacent river basins

FIGURE 2 | Knodus guajajara, paratypes. A. CICCAA 1518, 22.8 mm SL, Brazil, Maranhão, Alto Alegre do Pindaré municipality, igarapé Jenipapo, Pindaré River drainage, Mearim River basin. B. CICCAA 2696, 40.2 mm SL, Brazil, Maranhão, Chapadinha municipality, stream in riparian forest on the road BR–222, Munim River basin.

FIGURE 3 in A new species of Knodus (Characiformes: Characidae), with deep genetic divergence, from the Mearim and Munim river basins, Northeastern Brazil, and evidence for hidden diversity in adjacent river basins

FIGURE 3 | Knodus guajajara, CICCAA 4861, paratype, 31.9 mm SL, jaw suspensorium. A. Premaxillary. B. Maxilla. C. Dentary. Scale bar = 1 mm.

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Linked collectors and determiners for: A new species of Uroplatus (Gekkonidae) from Ankarana National Park Madagascar, of remarkably high genetic divergence.

Natural history specimen data linked to collectors and determiners held within, "A new species of Uroplatus (Gekkonidae) from Ankarana National Park Madagascar, of remarkably high genetic divergence". Claims or attributions were made on Bionomia by volunteer Scribes, <a href="https://bionomia.net/dataset/d1087ef4-03bc-4656-887b-506a0f972c08">https://bionomia.net/dataset/d1087ef4-03bc-4656-887b-506a0f972c08</a> using specimen data from the dataset aggregated by the Global Biodiversity Information Facility, <a href="https://gbif.org/dataset/d1087ef4-03bc-4656-887b-506a0f972c08">https://gbif.org/dataset/d1087ef4-03bc-4656-887b-506a0f972c08</a>. Formatted as a Frictionless Data package.

opencc-zeroJan 2024View details →

Linked collectors and determiners for: Validation of the status of a species with high CO 1 and low nuclear genetic divergences: the scab mite Caparinia ictonyctis stat. res. (Acariformes: Psoroptidae) parasitizing the African hedgehog Atelerix albiventris.

Natural history specimen data linked to collectors and determiners held within, "Validation of the status of a species with high CO 1 and low nuclear genetic divergences: the scab mite Caparinia ictonyctis stat. res. (Acariformes: Psoroptidae) parasitizing the African hedgehog Atelerix albiventris". Claims or attributions were made on Bionomia by volunteer Scribes, <a href="https://bionomia.net/dataset/3f253e3e-777e-465d-841d-a67e3b645d1a">https://bionomia.net/dataset/3f253e3e-777e-465d-841d-a67e3b645d1a</a> using specimen data from the dataset aggregated by the Global Biodiversity Information Facility, <a href="https://gbif.org/dataset/3f253e3e-777e-465d-841d-a67e3b645d1a">https://gbif.org/dataset/3f253e3e-777e-465d-841d-a67e3b645d1a</a>. Formatted as a Frictionless Data package.

Figure 12 in Morphological, vocal and genetic divergence in the Cettia acanthizoides complex (Aves: Cettiidae)

Figure 12. Two strophes of a less common type of song of Cettia brunnescens, West Bengal, India, May; same individual as in Figure 8; tape recording by Per Alström.

Figure 10. A cut from part II in Morphological, vocal and genetic divergence in the Cettia acanthizoides complex (Aves: Cettiidae)

Figure 10. A cut from part II and the beginning of part III of the song of Cettia brunnescens, West Bengal, India, May, different individual compared with Figures 8 and 9. Tape recording by Per Alström.

Figure 11. A in Morphological, vocal and genetic divergence in the Cettia acanthizoides complex (Aves: Cettiidae)

Figure 11. A, one song strophe of Cettia brunnescens, Uttaranchal, India, June; tape recording by Pratap Singh. B, the same recording as that shown in (A) but with the detail from part II at a higher time resolution. C, a different song strophe from the same individual. Detail from part II at a higher time resolution.

Figure 7 in Morphological, vocal and genetic divergence in the Cettia acanthizoides complex (Aves: Cettiidae)

Figure 7. One song strophe of Cettia brunnescens, Arunachal Pradesh, India, June; tape recording by Pratap Singh.

Figure 9 in Morphological, vocal and genetic divergence in the Cettia acanthizoides complex (Aves: Cettiidae)

Figure 9. One song strophe of Cettia brunnescens, West Bengal, India, May; tape recording by Per Alström.

Figure 8. A in Morphological, vocal and genetic divergence in the Cettia acanthizoides complex (Aves: Cettiidae)

Figure 8. A, one song strophe of Cettia brunnescens, West Bengal, India, May; tape recording by Per Alström. This is from a different individual than the song strophe shown in Figure 9. B, the same recording as that shown in (A) but with the detail from part II and the beginning of part III at a higher time resolution.

Figure 3 in Morphological, vocal and genetic divergence in the Cettia acanthizoides complex (Aves: Cettiidae)

Figure 3. One song strophe of Cettia a. acanthizoides, Shaanxi, China, June; tape recording by Per Alström.

Figure 2 in Morphological, vocal and genetic divergence in the Cettia acanthizoides complex (Aves: Cettiidae)

Figure 2. Plot of canonical scores from discriminant functions analysis between members of the Cettia acanthizoides group.

Figure 14. Cytochrome b in Morphological, vocal and genetic divergence in the Cettia acanthizoides complex (Aves: Cettiidae)

Figure 14. Cytochrome b tree of the three taxa in the Cettia acanthizoides complex and Cettia cetti albiventris, rooted with Phylloscopus chloronotus, estimated by Bayesian inference under the GTR + I model. Posterior probabilities (81 000 trees) are shown above nodes, and parsimony bootstrap values (1000 replicates) are shown below nodes.

Figure 5. A in Morphological, vocal and genetic divergence in the Cettia acanthizoides complex (Aves: Cettiidae)

Figure 5. A, one song strophe of Cettia a. acanthizoides, Fujian, China, May; tape recording by Per Alström. B, the same recording as that shown in (A) but with the detail from part II at a higher time resolution.