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Tetrastylis ovalis: A second case of bat-pollinated passionflower (Passifloraceae)

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/j.1537-2197.1979.tb06295.xopenalex-snapshot
VISCIN THREADS, POLLINATION EFFICIENCY AND LOW POLLEN‐OVULE RATIOS
inferredcites →https://doi.org/10.1007/978-1-4613-3421-7_8openalex-snapshot
Foraging Strategies of Plant-Visiting Bats
inferredcites →https://doi.org/10.1007/bf01290033openalex-snapshot
Fledermausblumen in S�damerika
inferredcites →https://doi.org/10.1016/c2009-0-00736-3openalex-snapshot
Principles of Pollination Ecology
inferredcites →https://doi.org/10.1016/s0367-1801(17)30097-2openalex-snapshot
Chiropterophilie in der neotropischen Flora
inferredcites →https://doi.org/10.1016/s0367-1801(17)30208-9openalex-snapshot
Chiropterophilie in der neotropischen Flora Neue Mitteilungen II
inferredcites →https://doi.org/10.1016/s0367-1801(17)30220-xopenalex-snapshot
Chiropterophilie in der neotropischen Flora Neue Mitteilungen III )
inferredcites →https://doi.org/10.1016/s0367-2530(17)31166-0openalex-snapshot
Bat Visits to Marcgravia myriostigma Tr. et Planch. (Marcgraviaceae) in Southeastern Brazil
inferredcites →https://doi.org/10.1038/071026a0openalex-snapshot
Handbuch der Blütenbiologie
inferredcites →https://doi.org/10.1038/270509a0openalex-snapshot
Time sharing and body partitioning in bat–plant pollination systems
inferredcites →https://doi.org/10.1086/403276openalex-snapshot
The Adaptation of Flowering Plants to Nocturnal and Crepuscular Pollinators
inferredcites →https://doi.org/10.1111/j.1558-5646.1975.tb00861.xopenalex-snapshot
COEVOLUTION OF PLANTS AND HERBIVORES: PASSION FLOWER BUTTERFLIES
inferredcites →https://doi.org/10.1163/156853968x00072openalex-snapshot
Reproductive Behavior in the Passifloraceae and Some of Its Pollinators in Central America
inferredcites →https://doi.org/10.2307/1218360openalex-snapshot
Vascular Plant Systematics
inferredcites →https://doi.org/10.2307/1935229openalex-snapshot
Bat Activity and Pollination of Bauhinia Pauletia: Plant‐Pollinator Coevolution
inferredcites →https://doi.org/10.2307/2259009openalex-snapshot
Tropical Forest Ecosystems in Africa and South America: a Comparative Review.
inferredcites →https://doi.org/10.2307/2388012openalex-snapshot
Bat Pollination of the Passion Flower, Passiflora mucronata, in Southeastern Brazil
inferredcites →https://doi.org/10.5962/bhl.title.2269openalex-snapshot
The American species of Passifloraceae

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.11646/phytotaxa.132.1.3zenodo-depositor-declared
A Molecular Systematic Analysis of Passiflora ovalis and Passiflora contracta (Passifloraceae)
inferred← citeshttps://doi.org/10.1002/j.1537-2197.1995.tb13855.xopenalex-snapshot
Ecological constraints on fruit initiation by Calyptrogyne ghiesbreghtiana (Arecaceae): FLORAL HERBIVORY, POLLEN AVAILABILITY, AND VISITATION BY POLLINATING BATS
inferred← citeshttps://doi.org/10.1006/anbo.1999.0876openalex-snapshot
Bat-pollinated Flower Assemblages and Bat Visitors at Two Atlantic Forest Sites in Brazil
inferred← citeshttps://doi.org/10.1007/978-3-7091-0286-2_1openalex-snapshot
Bonding Single Pollen Grains Together: How and Why?
inferred← citeshttps://doi.org/10.1007/978-3-7091-6306-1_15openalex-snapshot
Thread-forming structures in angiosperm anthers: their diverse role in pollination ecology
inferred← citeshttps://doi.org/10.1007/bf00984107openalex-snapshot
Thread-forming structures in angiosperm anthers: Their diverse role in pollination ecology
inferred← citeshttps://doi.org/10.1007/bf00984668openalex-snapshot
Nectar by day and night:Siphocampylus sulfureus (Lobeliaceae) pollinated by hummingbirds and bats
inferred← citeshttps://doi.org/10.1007/s00360-004-0442-4openalex-snapshot
The power requirements (Glossophaginae: Phyllostomidae) in nectar-feeding bats for clinging to flowers
inferred← citeshttps://doi.org/10.1007/s00606-013-0961-0openalex-snapshot
Floral ontogeny in Passiflora lobata (Malpighiales, Passifloraceae) reveals a rare pattern in petal formation and provides new evidence for interpretation of the tendril and corona
inferred← citeshttps://doi.org/10.1007/s00606-017-1390-2openalex-snapshot
Morphological characterization in the genus Passiflora L.: an approach to understanding its complex variability
inferred← citeshttps://doi.org/10.1007/s12229-021-09257-zopenalex-snapshot
The Calix Tube and Floral Nectar Tissue in Passiflora L.: What Can they Tell us about the Flower Structure Evolution?
inferred← citeshttps://doi.org/10.1016/j.flora.2022.152114openalex-snapshot
Divergent strategies of nectar secretion in two bat-pollinated Passiflora species
inferred← citeshttps://doi.org/10.1016/j.ympev.2016.05.013openalex-snapshot
Could refuge theory and rivers acting as barriers explain the genetic variability distribution in the Atlantic Forest?
inferred← citeshttps://doi.org/10.1023/a:1021331711108openalex-snapshot
A Phylogeny of the Neotropical Nectar-Feeding Bats (Chiroptera: Phyllostomidae) Based on Morphological and Molecular Data
inferred← citeshttps://doi.org/10.1080/00173139709362583openalex-snapshot
Pollen‐connecting threads inGymnocalycium(Cactaceae): Their origin, function, and systematic relevance
inferred← citeshttps://doi.org/10.1086/711080openalex-snapshot
“Sweet Rain” from Bat-Pollinated Flowers: How Does Sugar Concentration Modulate Nectar Retention?
inferred← citeshttps://doi.org/10.1093/botlinnean/box094openalex-snapshot
Genetic variability and population structure of Passiflora contracta, a bat-pollinated species from a fragmented rainforest
inferred← citeshttps://doi.org/10.1111/ele.70221openalex-snapshot
Ecological Niche Structure and the Interactive Role of Leaf‐Nosed Bats (Chiroptera: Phyllostomidae) Within Frugivory Networks: Another Dimension of the Niche Centroid Hypothesis
inferred← citeshttps://doi.org/10.1111/j.1744-7429.2001.tb00229.xopenalex-snapshot
Observations on the Pollination of Passiflora penduliflora
inferred← citeshttps://doi.org/10.1111/j.1744-7429.2002.tb00552.xopenalex-snapshot
Flower Visitation by Bats in Cloud Forests of Western Ecuador1
inferred← citeshttps://doi.org/10.1111/plb.12295openalex-snapshot
Auxin and physical constraint exerted by the perianth promote androgynophore bending in Passiflora mucronata L. (Passifloraceae)
inferred← citeshttps://doi.org/10.11606/d.11.2019.tde-20191218-120745openalex-snapshot
Ecologia da polinização, fluxo de pólen e taxa de cruzamento em >i /i< Link. (Caesalpiniaceae)
inferred← citeshttps://doi.org/10.11606/t.11.2020.tde-04062020-160041openalex-snapshot
Chloroplast genome evolution in >i /i<
inferred← citeshttps://doi.org/10.11606/t.41.2020.tde-15122020-140502openalex-snapshot
Organização das comunidades de flores e polinizadores vertebrados na Mata Atlântica brasileira
inferred← citeshttps://doi.org/10.1186/s12870-025-06210-9openalex-snapshot
Chloroplast genomic insights into adaptive evolution and rapid radiation in the genus Passiflora (Passifloraceae)
inferred← citeshttps://doi.org/10.13102/sociobiology.v60i3.295-305openalex-snapshot
Comparing the Structure and Robustness of Passifloraceae - Floral Visitor and True Pollinator Networks in a Lowland Atlantic Forest
inferred← citeshttps://doi.org/10.1515/mammalia-2025-0039openalex-snapshot
On the diet of Rhinophylla alethina (Chiroptera: Phyllostomidae) and congenerics
inferred← citeshttps://doi.org/10.1590/2236-8906-70/2019openalex-snapshot
Análise de pólen em pelagem de morcegos Phyllostomidae (Chiroptera) no Parque Estadual Fontes do Ipiranga, São Paulo, SP, Brasil
inferred← citeshttps://doi.org/10.1590/s0100-84041997000200002openalex-snapshot
Biologia floral de cinco espécies de Passiflora L. (Passifloraceae) em mata semidecídua
inferred← citeshttps://doi.org/10.1590/s0102-33062010000100028openalex-snapshot
Biologia reprodutiva de Passiflora capsularis L. e P. pohlii Mast. (Decaloba, Passifloraceae)
inferred← citeshttps://doi.org/10.1590/s1519-69842006000400019openalex-snapshot
Effect of nectar secretion rate on pollination success of Passiflora coccinea (Passifloraceae) in the Central Amazon
inferred← citeshttps://doi.org/10.1644/791.1openalex-snapshot
Rhinophylla pumilio
inferred← citeshttps://doi.org/10.1646/0006-3606(2001)033[0709:ootpop]2.0.co;2openalex-snapshot
Observations on the Pollination of Passiflora penduliflora1
inferred← citeshttps://doi.org/10.1646/0006-3606(2002)034[0387:fvbbic]2.0.co;2openalex-snapshot
Flower Visitation by Bats in Cloud Forests of Western Ecuador1
inferred← citeshttps://doi.org/10.1663/0007-196x(2004)056[0089:ansopi]2.0.co;2openalex-snapshot
A new species of Passiflora in section Tetrastylis (Passifloraceae) and two overlooked species of Passiflora from Brazil
inferred← citeshttps://doi.org/10.3390/ijms130911343openalex-snapshot
Isolation and Characterization of Microsatellite Markers for Passiflora contracta
inferred← citeshttps://doi.org/10.3417/2011095openalex-snapshot
Passiflora unipetala, a New Bat-pollinated Species ofPassiflorasupersect.Tacsonia(Passifloraceae)
inferred← citeshttps://doi.org/10.4081/fe.2018.286openalex-snapshot
Flower visitation of Passiflora apetala, P. auriculata and P. holosericea (Passifloraceae) by Pepsis aquila (Hymenoptera: Pompilidae)
inferred← citeshttps://doi.org/10.47749/t/unicamp.2004.300253openalex-snapshot
Ecologia da polinização de Mucuna SP. NOV. (Fabaceae) no litoral norte de São Paulo, Brasil
inferred← citeshttps://doi.org/10.47749/t/unicamp.2022.1243012openalex-snapshot
Influência hormonal na ontogênese in vitro da corona em Passiflora spp
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