Evidence map›Paper›PMID 36329815›Full record

ArticleEcology and evolution2022

Climate and forest loss interactively restructure trait composition across a human-modified landscape.

Meghna Krishnadas

Abstract read
In one paragraph

Article in Ecology and evolution, 2022. 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
–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

1 citing paper in PubMed.

  1. 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

1 author.

Meghna KrishnadasCSIR- Centre for Cellular and Molecular Biology Hyderabad Telangana India.ORCID https://orcid.org/0000-0003-2231-9787

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Traits determine species response to climate conditions and the match between phenotypes and climate mediates spatial variation in species composition. These trait-climate linkages can be disrupted in human-modified landscapes. Human land use creates forest fragments where dispersal limitation or edge effects exclude species that may otherwise suit a given macroclimate. Furthermore, stressful macroclimate can limit viable trait combinations such that only a subset of values of any given trait occurs with respect to another trait, resulting in stronger trait covariance. Because forest loss can compound climatic stress, trait covariance from benign to harsher climates is expected to be stronger in fragments compared to contiguous forests. In a wet tropical forest landscape in the Western Ghats Biodiversity Hotspot of peninsular India, I compared fragments with adjacent contiguous forests for signatures of trait-mediated assembly of tree communities. Using four key plant traits-seed size, specific leaf area (SLA), wood density, and maximum height-I evaluated trait-abundance associations and trait covariance across climate, soil, and elevation gradients. In the contiguous forest, smaller-seeded, shorter, thinner-leaved species became more abundant from low to high elevations. In fragments, species with higher SLA were more abundant at sites with more seasonal climates and lower precipitation, and larger seeded species were less abundant at warmer sites. However, traits only weakly predicted abundances in both habitats. Moreover, only contiguous forests exhibited significant compositional change via traits, driven by trait syndromes varying along a composite gradient defined by elevation, water deficit, and soil C:N ratio. Site-level trait covariance revealed that warmer, wetter conditions in fragments favored taller species for given seed size, as compared to similar conditions in contiguous forests. Overall, trait syndromes and trait covariance, rather than single traits, determined the phenotypes best suited to macroclimate conditions and should inform management or restoration goals in fragments.

Indexed as

fragmentshuman‐modified forestplant communitytrait–climatetrait covariance

Identifiers

PMID36329815
PMCPMC9618670

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LicenceCC BY
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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.