Evidence map›Paper›PMID 27318689›Full record

ArticleJournal of chemical ecology2016

Ant and Mite Diversity Drives Toxin Variation in the Little Devil Poison Frog.

Jenna R McGugan, Gary D Byrd, Alexandre B Roland, Stephanie N Caty, Nisha Kabir, Elicio E Tapia, Sunia A Trauger, Luis A Coloma, Lauren A O'Connell

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Article in Journal of chemical ecology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing 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

27 citing papers in PubMed.

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  19. Rapid toxin sequestration modifies poison frog physiology.The Journal of experimental biology · 2021
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors.

Jenna R McGuganCenter for Systems Biology, Harvard University, Cambridge, MA, 02138, USA.
Gary D ByrdSmall Molecule Mass Spectrometry Facility, Harvard University, Cambridge, MA, 02138, USA.
Alexandre B RolandCenter for Systems Biology, Harvard University, Cambridge, MA, 02138, USA.
Stephanie N CatyCenter for Systems Biology, Harvard University, Cambridge, MA, 02138, USA.
Nisha KabirCambridge Rindge and Latin High School, Cambridge, MA, 02138, USA.
Elicio E TapiaCentro Jambatu de Investigación y Conservación de Anfibios, Fundación Otonga, Quito, Ecuador.
Sunia A TraugerSmall Molecule Mass Spectrometry Facility, Harvard University, Cambridge, MA, 02138, USA.
Luis A ColomaCentro Jambatu de Investigación y Conservación de Anfibios, Fundación Otonga, Quito, Ecuador.
Lauren A O'ConnellCenter for Systems Biology, Harvard University, Cambridge, MA, 02138, USA. aloconnell@fas.harvard.edu.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Poison frogs sequester chemical defenses from arthropod prey, although the details of how arthropod diversity contributes to variation in poison frog toxins remains unclear. We characterized skin alkaloid profiles in the Little Devil poison frog, Oophaga sylvatica (Dendrobatidae), across three populations in northwestern Ecuador. Using gas chromatography/mass spectrometry, we identified histrionicotoxins, 3,5- and 5,8-disubstituted indolizidines, decahydroquinolines, and lehmizidines as the primary alkaloid toxins in these O. sylvatica populations. Frog skin alkaloid composition varied along a geographical gradient following population distribution in a principal component analysis. We also characterized diversity in arthropods isolated from frog stomach contents and confirmed that O. sylvatica specialize on ants and mites. To test the hypothesis that poison frog toxin variability reflects species and chemical diversity in arthropod prey, we (1) used sequencing of cytochrome oxidase 1 to identify individual prey specimens, and (2) used liquid chromatography/mass spectrometry to chemically profile consumed ants and mites. We identified 45 ants and 9 mites in frog stomachs, including several undescribed species. We also showed that chemical profiles of consumed ants and mites cluster by frog population, suggesting different frog populations have access to chemically distinct prey. Finally, by comparing chemical profiles of frog skin and isolated prey items, we traced the arthropod source of four poison frog alkaloids, including 3,5- and 5,8-disubstituted indolizidines and a lehmizidine alkaloid. Together, the data show that toxin variability in O. sylvatica reflects chemical diversity in arthropod prey.

Indexed as

AntsBiodiversityMitesAlkaloidsAnimalsAnuraCyclooxygenase 1DietPredatory BehaviorToxins, BiologicalAlkaloidsCyclooxygenase 1Toxins, BiologicalAlkaloidAntDendrobatidaeMass spectrometryMitePoison frogToxin

Identifiers

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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.