Evidence map›Paper›PMID 37417448›Full record

ArticleAnnals of botany2023

Clonality, local population structure and gametophyte sex ratios in cryptic species of the Sphagnum magellanicum complex.

A Jonathan Shaw, Aaron M Duffy, Marta Nieto-Lugilde, Blanka Aguero, Scott Schuette, Sean Robinson, James Loveland, Karen A Hicks, David Weston, Bryan Piatkowski and 3 more

Open access · greenAbstract read
In one paragraph

Article in Annals of botany, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
7.3field-weighted citation impact, top 3% of its field
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

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.

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed, 12 citations in OpenAlex.

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4 · The record

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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

13 authors at 7 institutions in 2 countries.

A Jonathan ShawDepartment of Biology & L. E. Anderson Bryophyte Herbarium, Duke University, Durham, NC, 27708, USA.
Aaron M DuffyDepartment of Biology & L. E. Anderson Bryophyte Herbarium, Duke University, Durham, NC, 27708, USA.
Marta Nieto-LugildeDepartment of Biology & L. E. Anderson Bryophyte Herbarium, Duke University, Durham, NC, 27708, USA.
Blanka AgueroDepartment of Biology & L. E. Anderson Bryophyte Herbarium, Duke University, Durham, NC, 27708, USA.
Scott SchuettePennsylvania Natural Heritage Program, Western Pennsylvania Conservancy, Pittsburgh, PA, 15222, USA.
Sean RobinsonDepartment of Biology, SUNY Oneonta, Oneonta, NY, 13820, USA.
James LovelandDepartment of Biology, Kenyon College, Gambier, OH 43022, USA.
Karen A HicksDepartment of Biology, Kenyon College, Gambier, OH 43022, USA.
David WestonBiosciences Division, Oak Ridge National Laboratory, Oak Ridge, TN 37831, USA.
Bryan PiatkowskiBiosciences Division, Oak Ridge National Laboratory, Oak Ridge, TN 37831, USA.ORCID 0000-0002-1334-8431
Max KoltonThe Jacob Blaustein Institutes for Desert Research, Ben-Gurion University of the Negev, Midreshet Ben-Gurion, 8499000, Israel.ORCID 0000-0002-8166-3572
Joel E KoskaCenter for Microbial Dynamics and Infection, Georgia Institute of Technology, Atlanta, GA 30332, USA.
Adam L HealeyHudsonAlpha Institute for Biotechnology, Huntsville, AL 35806, USA.
Duke University · USKenyon College · USOak Ridge National Laboratory · USBen-Gurion University of the Negev · ILGeorgia Institute of Technology · USHudsonAlpha Institute for Biotechnology · USSUNY Oneonta · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND AND

aimsSphagnum (peatmoss) comprises a moss (Bryophyta) clade with ~300-500 species. The genus has unparalleled ecological importance because Sphagnum-dominated peatlands store almost a third of the terrestrial carbon pool and peatmosses engineer the formation and microtopography of peatlands. Genomic resources for Sphagnum are being actively expanded, but many aspects of their biology are still poorly known. Among these are the degree to which Sphagnum species reproduce asexually, and the relative frequencies of male and female gametophytes in these haploid-dominant plants. We assess clonality and gametophyte sex ratios and test hypotheses about the local-scale distribution of clones and sexes in four North American species of the S. magellanicum complex. These four species are difficult to distinguish morphologically and are very closely related. We also assess microbial communities associated with Sphagnum host plant clones and sexes at two sites.

methodsFour hundred and five samples of the four species, representing 57 populations, were subjected to restriction site-associated DNA sequencing (RADseq). Analyses of population structure and clonality based on the molecular data utilized both phylogenetic and phenetic approaches. Multi-locus genotypes (genets) were identified using the RADseq data. Sexes of sampled ramets were determined using a molecular approach that utilized coverage of loci on the sex chromosomes after the method was validated using a sample of plants that expressed sex phenotypically. Sex ratios were estimated for each species, and populations within species. Difference in fitness between genets was estimated as the numbers of ramets each genet comprised. Degrees of clonality [numbers of genets/numbers of ramets (samples)] within species, among sites, and between gametophyte sexes were estimated. Sex ratios were estimated for each species, and populations within species. Sphagnum-associated microbial communities were assessed at two sites in relation to Sphagnum clonality and sex. KEY

resultsAll four species appear to engage in a mixture of sexual and asexual (clonal) reproduction. A single ramet represents most genets but two to eight ramets were dsumbers ansd text etected for some genets. Only one genet is represented by ramets in multiple populations; all other genets are restricted to a single population. Within populations ramets of individual genets are spatially clustered, suggesting limited dispersal even within peatlands. Sex ratios are male-biased in S. diabolicum but female-biased in the other three species, although significantly so only in S. divinum. Neither species nor males/females differ in levels of clonal propagation. At St Regis Lake (NY) and Franklin Bog (VT), microbial community composition is strongly differentiated between the sites, but differences between species, genets and sexes were not detected. Within S. divinum, however, female gametophytes harboured two to three times the number of microbial taxa as males.

conclusionsThese four Sphagnum species all exhibit similar reproductive patterns that result from a mixture of sexual and asexual reproduction. The spatial patterns of clonally replicated ramets of genets suggest that these species fall between the so-called phalanx patterns, where genets abut one another but do not extensively mix because of limited ramet fragmentation, and the guerrilla patterns, where extensive genet fragmentation and dispersal result in greater mixing of different genets. Although sex ratios in bryophytes are most often female-biased, both male and female biases occur in this complex of closely related species. The association of far greater microbial diversity for female gametophytes in S. divinum, which has a female-biased sex ratio, suggests additional research to determine if levels of microbial diversity are consistently correlated with differing patterns of sex ratio biases.

Indexed as

Genetic VariationSphagnopsidaGerm Cells, PlantPhylogenyClonalitypeatlandspeatmossessex ratiosSphagnumSphagnum diabolicumSphagnum divinumSphagnum magniaeSphagnum medium

Identifiers

PMID37417448
PMCPMC10550268
OpenAlexW4383481242

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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.