Evidence map›Paper›PMID 34178110›Full record

ArticleEvolutionary applications2021

Leveraging genomics to understand threats to migratory birds.

Brenda Larison, Alec R Lindsay, Christen Bossu, Michael D Sorenson, Joseph D Kaplan, David C Evers, James Paruk, Jeffrey M DaCosta, Thomas B Smith, Kristen Ruegg

Abstract read
In one paragraph

Article in Evolutionary applications, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

10 authors.

Brenda LarisonDepartment of Ecology and Evolutionary Biology University of California Los Angeles California USA.ORCID https://orcid.org/0000-0002-0264-7276
Alec R LindsayDepartment of Biology Northern Michigan University Marquette Michigan USA.
Christen BossuDepartment of Biology Colorado State University Fort Collins Colorado USA.
Michael D SorensonDepartment of Biology Boston University Boston Massachusetts USA.
Joseph D KaplanCommon Coast Research and Conservation Hancock Michigan USA.
David C EversBiodiversity Research Institute Portland Maine USA.
James ParukBiology Department Saint Joseph's College Standish Maine USA.
Jeffrey M DaCostaBiology Department Boston College Chestnut Hill Massachusetts USA.
Thomas B SmithDepartment of Ecology and Evolutionary Biology University of California Los Angeles California USA.ORCID https://orcid.org/0000-0002-5978-6912
Kristen RueggDepartment of Biology Colorado State University Fort Collins Colorado USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Understanding how risk factors affect populations across their annual cycle is a major challenge for conserving migratory birds. For example, disease outbreaks may happen on the breeding grounds, the wintering grounds, or during migration and are expected to accelerate under climate change. The ability to identify the geographic origins of impacted individuals, especially outside of breeding areas, might make it possible to predict demographic trends and inform conservation decision-making. However, such an effort is made more challenging by the degraded state of carcasses and resulting low quality of DNA available. Here, we describe a rapid and low-cost approach for identifying the origins of birds sampled across their annual cycle that is robust even when DNA quality is poor. We illustrate the approach in the common loon (

Indexed as

botulismCommon Loonconservation genomicsdiseaseGavia immerRAD sequencingwaterbirdswildlife management

Identifiers

PMID34178110
PMCPMC8210798

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.