taxonID	type	format	identifier	references	title	description	created	creator	contributor	publisher	audience	source	license	rightsHolder	datasetID
03A6046A5345FF81FE66FEB6FA80F9B3.taxon	http://purl.org/dc/dcmitype/StillImage	image/png	https://zenodo.org/record/15536454/files/figure.png	https://doi.org/10.5281/zenodo.15536454	FIGURE 2 | Karyotypes of Hypostomus boulengeri subjected to A. Giemsa, B. C-banding and G. FISH with 18S rDNA probe (yellow). Polymorphism of the heterochromatin in pairs 24, 25, and 26 are shown in C, D, E, and F. The Ag-NOR- bearing chromosomes are boxed beside the karyotype stained with Giemsa. The B microchromosomes are boxed beside the karyotypes stained with Giemsa and C-banding. Scale bar = 10 µm.	FIGURE 2 | Karyotypes of Hypostomus boulengeri subjected to A. Giemsa, B. C-banding and G. FISH with 18S rDNA probe (yellow). Polymorphism of the heterochromatin in pairs 24, 25, and 26 are shown in C, D, E, and F. The Ag-NOR- bearing chromosomes are boxed beside the karyotype stained with Giemsa. The B microchromosomes are boxed beside the karyotypes stained with Giemsa and C-banding. Scale bar = 10 µm.	2024-07-22	Paiva, Suzana de;Porto, Fernanda Errero;Codognotto, Flávio José;Fernandes, Carlos Alexandre;Rossi, Margarida Maria Vieira;Borin-Carvalho, Luciana Andreia;Portela-Castro, Ana Luiza de Brito;Zawadzki, Claudio Henrique;Renesto, Erasmo;Martins-Santos, Isabel Cristina		Zenodo	biologists	Paiva, Suzana de;Porto, Fernanda Errero;Codognotto, Flávio José;Fernandes, Carlos Alexandre;Rossi, Margarida Maria Vieira;Borin-Carvalho, Luciana Andreia;Portela-Castro, Ana Luiza de Brito;Zawadzki, Claudio Henrique;Renesto, Erasmo;Martins-Santos, Isabel Cristina			
03A6046A5345FF81FE66FEB6FA80F9B3.taxon	http://purl.org/dc/dcmitype/StillImage	image/png	https://zenodo.org/record/15536456/files/figure.png	https://doi.org/10.5281/zenodo.15536456	FIGURE 3 | Karyotypes of Hypostomus cochliodon subjected to A. Giemsa, B. C-banding, and C. FISH with 18S rDNA probe (yellow). The Ag-NOR-bearing chromosomes are boxed beside the karyotype stained with Giemsa. Note one of the homologs of pair 29 with marking in both telomeres after stained Ag-NOR (Box in A), C-banding (Box in B), and FISH with 18S rDNA probe (Box in C). Scale bar = 10 µm.	FIGURE 3 | Karyotypes of Hypostomus cochliodon subjected to A. Giemsa, B. C-banding, and C. FISH with 18S rDNA probe (yellow). The Ag-NOR-bearing chromosomes are boxed beside the karyotype stained with Giemsa. Note one of the homologs of pair 29 with marking in both telomeres after stained Ag-NOR (Box in A), C-banding (Box in B), and FISH with 18S rDNA probe (Box in C). Scale bar = 10 µm.	2024-07-22	Paiva, Suzana de;Porto, Fernanda Errero;Codognotto, Flávio José;Fernandes, Carlos Alexandre;Rossi, Margarida Maria Vieira;Borin-Carvalho, Luciana Andreia;Portela-Castro, Ana Luiza de Brito;Zawadzki, Claudio Henrique;Renesto, Erasmo;Martins-Santos, Isabel Cristina		Zenodo	biologists	Paiva, Suzana de;Porto, Fernanda Errero;Codognotto, Flávio José;Fernandes, Carlos Alexandre;Rossi, Margarida Maria Vieira;Borin-Carvalho, Luciana Andreia;Portela-Castro, Ana Luiza de Brito;Zawadzki, Claudio Henrique;Renesto, Erasmo;Martins-Santos, Isabel Cristina			
