Evidence map›Paper›PMID 25227258›Full record

ArticleHeredity2015

O father where art thou? Paternity analyses in a natural population of the haploid-diploid seaweed Chondrus crispus.

S A Krueger-Hadfield, D Roze, J A Correa, C Destombe, M Valero

Abstract read
In one paragraph

Article in Heredity, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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

18 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Evolution of parental care in haploid-diploid plants.Proceedings. Biological sciences · 2024
    Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Inbreeding shapes the evolution of marine invertebrates.Evolution; international journal of organic evolution · 2020
    Article
  14. Article
  15. Article
  16. Article
  17. Sexual selection in hermaphrodites, sperm and broadcast spawners, plants and fungi.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2016
    Review
  18. 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

5 authors.

S A Krueger-Hadfield1] CNRS, UPMC University Paris 06, Sorbonne Universités, UMI 3614, Evolutionary Biology and Ecology of Algae, Station Biologique de Roscoff, Roscoff, France [2] Departamento de Ecología, Center for Advanced Studies in Ecology and Biodiversity, Facultad de Ciencias Biológicas, Pontificia Universidad Católica de Chile, Santiago, Chile.
D RozeCNRS, UPMC University Paris 06, Sorbonne Universités, UMI 3614, Evolutionary Biology and Ecology of Algae, Station Biologique de Roscoff, Roscoff, France.
J A CorreaDepartamento de Ecología, Center of Applied Ecology and Sustainability, Facultad de Ciencias Biológicas, Pontificia Universidad Católica de Chile, Santiago, Chile.
C DestombeCNRS, UPMC University Paris 06, Sorbonne Universités, UMI 3614, Evolutionary Biology and Ecology of Algae, Station Biologique de Roscoff, Roscoff, France.
M ValeroCNRS, UPMC University Paris 06, Sorbonne Universités, UMI 3614, Evolutionary Biology and Ecology of Algae, Station Biologique de Roscoff, Roscoff, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The link between life history traits and mating systems in diploid organisms has been extensively addressed in the literature, whereas the degree of selfing and/or inbreeding in natural populations of haploid-diploid organisms, in which haploid gametophytes alternate with diploid sporophytes, has been rarely measured. Dioecy has often been used as a proxy for the mating system in these organisms. Yet, dioecy does not prevent the fusion of gametes from male and female gametophytes originating from the same sporophyte. This is likely a common occurrence when spores from the same parent are dispersed in clumps and recruit together. This pattern of clumped spore dispersal has been hypothesized to explain significant heterozygote deficiency in the dioecious haploid-diploid seaweed Chondrus crispus. Fronds and cystocarps (structures in which zygotes are mitotically amplified) were sampled in two 25 m(2) plots located within a high and a low intertidal zone and genotyped at 5 polymorphic microsatellite loci in order to explore the mating system directly using paternity analyses. Multiple males sired cystocarps on each female, but only one of the 423 paternal genotypes corresponded to a field-sampled gametophyte. Nevertheless, larger kinship coefficients were detected between males siring cystocarps on the same female in comparison with males in the entire population, confirming restricted spermatial and clumped spore dispersal. Such dispersal mechanisms may be a mode of reproductive assurance due to nonmotile gametes associated with putatively reduced effects of inbreeding depression because of the free-living haploid stage in C. crispus.

Indexed as

ChondrusDiploidyGenetics, PopulationGenotypeGerm Cells, PlantHaploidyHomozygoteInbreedingMolecular Sequence DataReproduction

Identifiers

PMID25227258
PMCPMC4815628

What OpenQuestion holds

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Registered trials

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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.