taxonID	type	format	identifier	references	title	description	created	creator	contributor	publisher	audience	source	license	rightsHolder	datasetID
CF6A879D6E3D740166B8FD31DFFB0D30.taxon	http://purl.org/dc/dcmitype/StillImage	image/png	https://zenodo.org/record/195832/files/figure.png	https://doi.org/10.5281/zenodo.195832	FIGURE 2. Life aspects of: (A) Hyperolius veithi sp. nov. in amplexus (unidentified paratypes; photo J. Kielgast), note that there is a yellow spot on the heel visible in the male frog; (B) H. cinnamomeoventris male in PhJ from the type locality (AC 3008; photo A. Channing); (C) H. cinnamomeoventris female from the Kakamega Forest, Kenya (not collected; photo S. Lötters); (D) H. cinnamomeoventris male in PhJ from Semliki, Uganda (SL 555; photo A. Channing); (E) H. molleri from São Tomé (photo D. Lin, CAS) and (F) H. thomensis from São Tomé in amplexus (photo D. Lin, CAS).	FIGURE 2. Life aspects of: (A) Hyperolius veithi sp. nov. in amplexus (unidentified paratypes; photo J. Kielgast), note that there is a yellow spot on the heel visible in the male frog; (B) H. cinnamomeoventris male in PhJ from the type locality (AC 3008; photo A. Channing); (C) H. cinnamomeoventris female from the Kakamega Forest, Kenya (not collected; photo S. Lötters); (D) H. cinnamomeoventris male in PhJ from Semliki, Uganda (SL 555; photo A. Channing); (E) H. molleri from São Tomé (photo D. Lin, CAS) and (F) H. thomensis from São Tomé in amplexus (photo D. Lin, CAS).	2010-12-31	Schick, Susanne;Kielgast, Jos;Rödder, Dennis;Muchai, Vincent;Burger, Marius;Lötters, Stefan		Zenodo	biologists	Schick, Susanne;Kielgast, Jos;Rödder, Dennis;Muchai, Vincent;Burger, Marius;Lötters, Stefan			
CF6A879D6E3D740166B8FD31DFFB0D30.taxon	http://purl.org/dc/dcmitype/StillImage	image/png	https://zenodo.org/record/195834/files/figure.png	https://doi.org/10.5281/zenodo.195834	FIGURE 4. Dorsal and ventral views of preserved (A) male holotype of Hyperolius veithi sp. nov. (photos by F. Feß), SVL 26.3 mm, (B) female holotype of Hyperolius schoutedeni (photos by MRAC, through the courtesy of D. Meirte), SVL 26.4 mm.	FIGURE 4. Dorsal and ventral views of preserved (A) male holotype of Hyperolius veithi sp. nov. (photos by F. Feß), SVL 26.3 mm, (B) female holotype of Hyperolius schoutedeni (photos by MRAC, through the courtesy of D. Meirte), SVL 26.4 mm.	2010-12-31	Schick, Susanne;Kielgast, Jos;Rödder, Dennis;Muchai, Vincent;Burger, Marius;Lötters, Stefan		Zenodo	biologists	Schick, Susanne;Kielgast, Jos;Rödder, Dennis;Muchai, Vincent;Burger, Marius;Lötters, Stefan			
CF6A879D6E3D740166B8FD31DFFB0D30.taxon	http://purl.org/dc/dcmitype/StillImage	image/png	https://zenodo.org/record/195833/files/figure.png	https://doi.org/10.5281/zenodo.195833	FIGURE 3. Bayesian phylogram of Hyperolius species including Cinnamon-belly reed frogs inferred from nucleotide sequence data from 16 S mitochondrial rRNA. Bayesian posterior probabilities> 0.95 each are marked by an asterisk on branch. We here apply species names as given in Table 1; in the Cinnamon-belly reed frog clade, numbers in parentheses give sample size of the same haplotype, which corresponds with localities. Note that Hyperolius cinnamomeoventris is paraphyletic. Topotypic material of H. olivaceus (#) and H. cinnamomeoventris (##) are indicated. Hyperolius sp. ‘ Salonga’ is H. veithi sp. nov. Both the Hierarchical Likelihood Ratio Tests and Akaike Information Criterion implemented in MrModeltest selected a GTR + I + G model with a gamma distribution of 0.5912 and a proportion of invariable sites of 0.2291 (estimated base frequencies: A: 0.3294, C: 0.2260, G: 0.1813, T: 0.2633; rate matrix: A-C: 3.0708, A-G: 7.4382, A-T: 5.3616, C-G: 1.5864, C-T: 21.7283, G-T: 1.0000).	FIGURE 3. Bayesian phylogram of Hyperolius species including Cinnamon-belly reed frogs inferred from nucleotide sequence data from 16 S mitochondrial rRNA. Bayesian posterior probabilities> 0.95 each are marked by an asterisk on branch. We here apply species names as given in Table 1; in the Cinnamon-belly reed frog clade, numbers in parentheses give sample size of the same haplotype, which corresponds with localities. Note that Hyperolius cinnamomeoventris is paraphyletic. Topotypic material of H. olivaceus (#) and H. cinnamomeoventris (##) are indicated. Hyperolius sp. ‘ Salonga’ is H. veithi sp. nov. Both the Hierarchical Likelihood Ratio Tests and Akaike Information Criterion implemented in MrModeltest selected a GTR + I + G model with a gamma distribution of 0.5912 and a proportion of invariable sites of 0.2291 (estimated base frequencies: A: 0.3294, C: 0.2260, G: 0.1813, T: 0.2633; rate matrix: A-C: 3.0708, A-G: 7.4382, A-T: 5.3616, C-G: 1.5864, C-T: 21.7283, G-T: 1.0000).	2010-12-31	Schick, Susanne;Kielgast, Jos;Rödder, Dennis;Muchai, Vincent;Burger, Marius;Lötters, Stefan		Zenodo	biologists	Schick, Susanne;Kielgast, Jos;Rödder, Dennis;Muchai, Vincent;Burger, Marius;Lötters, Stefan			
CF6A879D6E3D740166B8FD31DFFB0D30.taxon	http://purl.org/dc/dcmitype/StillImage	image/png	https://zenodo.org/record/195831/files/figure.png	https://doi.org/10.5281/zenodo.195831	FIGURE 1. Map of Central Africa and adjacent areas showing Salonga National Park (white contour line), distribution of H. cinnamomeoventris according to the IUCN Red List (http: // www. iucnredlist. org) following the 2002 2004 IUCN Global Amphibian Assessment (bold black contour line) and localities of our genetic sampling from type localities (reverse filled triangle— H. cinnamomeoventris and H. tristis, white circle— H. veithi sp. nov., filled square— H. ituriensis, filled triangle— H. olivaceus and H. fimbriolatus) and additional localities (small filled dots). In addition, the type locality of H. wittei (cross) is shown. Note that H. veithi syntopically occurs with H. cinnamomeoventris.	FIGURE 1. Map of Central Africa and adjacent areas showing Salonga National Park (white contour line), distribution of H. cinnamomeoventris according to the IUCN Red List (http: // www. iucnredlist. org) following the 2002 2004 IUCN Global Amphibian Assessment (bold black contour line) and localities of our genetic sampling from type localities (reverse filled triangle— H. cinnamomeoventris and H. tristis, white circle— H. veithi sp. nov., filled square— H. ituriensis, filled triangle— H. olivaceus and H. fimbriolatus) and additional localities (small filled dots). In addition, the type locality of H. wittei (cross) is shown. Note that H. veithi syntopically occurs with H. cinnamomeoventris.	2010-12-31	Schick, Susanne;Kielgast, Jos;Rödder, Dennis;Muchai, Vincent;Burger, Marius;Lötters, Stefan		Zenodo	biologists	Schick, Susanne;Kielgast, Jos;Rödder, Dennis;Muchai, Vincent;Burger, Marius;Lötters, Stefan			
