Evidence map›Paper›PMID 25497514›Full record

ArticleAnnals of botany2015

Floral biology and ovule and seed ontogeny of Nymphaea thermarum, a water lily at the brink of extinction with potential as a model system for basal angiosperms.

Rebecca A Povilus, Juan M Losada, William E Friedman

Abstract read
In one paragraph

Article in Annals of botany, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

17 citing papers in PubMed.

  1. Floatable and Integrated Shape-shifting Hydrogel Carrier.Advanced materials (Deerfield Beach, Fla.) · 2026
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  4. Variation in the Floral Scent Chemistry ofPlants (Basel, Switzerland) · 2024
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  6. Model Species to Investigate the Origin of Flowers.Methods in molecular biology (Clifton, N.J.) · 2023
    Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Water lily (Proceedings of the National Academy of Sciences of the United States of America · 2020
    Article
  12. Review
  13. Seed coat thickness in the evolution of angiosperms.Cellular and molecular life sciences : CMLS · 2018
    Review
  14. Article
  15. Review
  16. Review
  17. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors.

Rebecca A PovilusDepartment of Organismic and Evolutionary Biology, Harvard University, 26 Oxford Street, Cambridge, MA 02138, USA and Arnold Arboretum of Harvard University, 1300 Centre Street, Boston, MA 02131, USA rpovilus@fas.harvard.edu.
Juan M LosadaDepartment of Organismic and Evolutionary Biology, Harvard University, 26 Oxford Street, Cambridge, MA 02138, USA and Arnold Arboretum of Harvard University, 1300 Centre Street, Boston, MA 02131, USA Department of Organismic and Evolutionary Biology, Harvard University, 26 Oxford Street, Cambridge, MA 02138, USA and Arnold Arboretum of Harvard University, 1300 Centre Street, Boston, MA 02131, USA.
William E FriedmanDepartment of Organismic and Evolutionary Biology, Harvard University, 26 Oxford Street, Cambridge, MA 02138, USA and Arnold Arboretum of Harvard University, 1300 Centre Street, Boston, MA 02131, USA Department of Organismic and Evolutionary Biology, Harvard University, 26 Oxford Street, Cambridge, MA 02138, USA and Arnold Arboretum of Harvard University, 1300 Centre Street, Boston, MA 02131, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND AND

aimsNymphaea thermarum is a member of the Nymphaeales, of one of the most ancient lineages of flowering plants. This species was only recently described and then declared extinct in the wild, so little is known about its reproductive biology. In general, the complete ontogeny of ovules and seeds is not well documented among species of Nymphaea and has never been studied in the subgenus Brachyceras, the clade to which N. thermarum belongs.

methodsFlowers and fruits were processed for brightfield, epifluorescence and confocal microscopy. Flower morphology, with emphasis on the timing of male and female functions, was correlated with key developmental stages of the ovule and the female gametophyte. Development of the seed tissues and dynamics of polysaccharide reserves in the endosperm, perisperm and embryo were examined. KEY

resultsPollen release in N. thermarum starts before the flower opens. Cell walls of the micropylar nucellus show layering of callose and cellulose in a manner reminiscent of transfer cell wall patterning. Endosperm development is ab initio cellular, with micropylar and chalazal domains that embark on distinct developmental trajectories. The surrounding maternal perisperm occupies the majority of seed volume and accumulates starch centrifugally. In mature seeds, a minute but fully developed embryo is surrounded by a single, persistent layer of endosperm.

conclusionsEarly male and female function indicate that N. thermarum is predisposed towards self-pollination, a phenomenon that is likely to have evolved multiple times within Nymphaea. While formation of distinct micropylar and chalazal developmental domains in the endosperm, along with a copious perisperm, characterize the seeds of most members of the Nymphaeales, seed ontogenies vary between and among the constituent families. Floral biology, life history traits and small genome size make N. thermarum uniquely promising as an early-diverging angiosperm model system for genetic and molecular studies.

Indexed as

Endangered SpeciesBiological EvolutionFlowersMagnoliopsidaNymphaeaOvuleSeedsEarly-diverging angiospermembryoendospermevo-devofemale gametophyteflower biologymegagametogenesismegasporogenesisNymphaealesNymphaea thermarumperispermprotogynyseed developmentstigma

Identifiers

PMID25497514
PMCPMC4551091

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.