2015
DOI: 10.1515/biolog-2015-0089
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Reproductive and cytogenetic characterization in Passiflora sublanceolata

Abstract: Reproductive biology (pollen-ovule ratio, pollen viability, germination in vitro pollination and stigma receptivity in vivo) and karyotype characterization by classical and molecular techniques were performed in Passiflora sublanceolata. The pollen-ovule ratio was 83.9, suggesting that this species is facultative autogamous. Pollen viability was below 70% during all anthesis period (6:00 a.m. to 12:00 p.m.). Low in vitro germination rates were observed after anthesis beginning, with none percentage at one, fou… Show more

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Cited by 11 publications
(6 citation statements)
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“…2001; Melo & Guerra 2003; Belo et al . 2015). Likewise, the position of P. foetida , based on molecular phylogeny, has always been problematic within the subgenus Passiflora (Muschner et al .…”
Section: Discussionmentioning
confidence: 99%
“…2001; Melo & Guerra 2003; Belo et al . 2015). Likewise, the position of P. foetida , based on molecular phylogeny, has always been problematic within the subgenus Passiflora (Muschner et al .…”
Section: Discussionmentioning
confidence: 99%
“…The presence of CMA3 + blocks in the terminal region of some chromosomes is generally related to the nucleolar organizing regions (NORs) observed in angiosperms (Guerra, 2000). In species of the genus Passiflora, GC-rich regions detected by fluorochrome CMA3 are observed only in 45S rDNA/satellite DNA sites (Melo et al, 2001;Viana & Souza, 2012;Melo et al, 2014;Belo et al, 2015). The distribution of satellite DNA/45S rDNA regarding CMA3 was analyzed in some species of the genus Citrus, and both probes hybridized only with CMA3 and the centromeres (Silva et al, 2010).…”
Section: Discussionmentioning
confidence: 99%
“…; Belo et al . ). However, a few exceptions can be seen, such as P. tricuspis with one additional GC‐rich block not related by secondary constriction (Melo et al .…”
Section: Discussionmentioning
confidence: 97%
“…The 5S rDNA and telomere probes were obtained by PCR with the primer pairs 5′‐GTGCGATCATACCAGC(AG)(CT)TAATGCACCGG‐3′ and 5′‐GAGGTGCAACACGAGGACTTCCCAGGAGG‐ 3′ for 5S rDNA (Melo & Guerra ) and 5′‐AAATCCCAAATCCCAAATCCCAAATCCCAAATCCCAAATCCC‐3′ and 5′‐TTTAGGGTTTAGGGTTTAGGGTTTAGGGTTTAGCGTTTAGG‐3′ for telomere sites (Belo et al . ). Probes constructed for 26S rDNA for the localisation of the 45S rDNA loci were obtained by PCR amplification with primers reported in Silva ().…”
Section: Methodsmentioning
confidence: 97%