Evidence map›Paper›PMID 32396811›Full record

ArticleJournal of the Royal Society, Interface2020

Sequential experimental design for predator-prey functional response experiments.

Hayden Moffat, Markus Hainy, Nikos E Papanikolaou, Christopher Drovandi

Abstract read
In one paragraph

Article in Journal of the Royal Society, Interface, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. 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

4 authors.

Hayden MoffatSchool of Mathematical Sciences, Queensland University of Technology, Brisbane, Australia.
Markus HainySchool of Mathematical Sciences, Queensland University of Technology, Brisbane, Australia.
Nikos E PapanikolaouDirectorate of Plant Protection, Greek Ministry of Rural Development and Food, Athens, Greece.
Christopher DrovandiSchool of Mathematical Sciences, Queensland University of Technology, Brisbane, Australia.

Funding

Austrian Science Fund FWF J 3959
6 · The paper itself

Abstract

Understanding functional response within a predator-prey dynamic is a cornerstone for many quantitative ecological studies. Over the past 60 years, the methodology for modelling functional response has gradually transitioned from the classic mechanistic models to more statistically oriented models. To obtain inferences on these statistical models, a substantial number of experiments need to be conducted. The obvious disadvantages of collecting this volume of data include cost, time and the sacrificing of animals. Therefore, optimally designed experiments are useful as they may reduce the total number of experimental runs required to attain the same statistical results. In this paper, we develop the first sequential experimental design method for predator-prey functional response experiments. To make inferences on the parameters in each of the statistical models we consider, we use sequential Monte Carlo, which is computationally efficient and facilitates convenient estimation of important utility functions. It provides coverage of experimental goals including parameter estimation, model discrimination as well as a combination of these. The results of our simulation study illustrate that for predator-prey functional response experiments sequential design outperforms static design for our experimental goals. R code for implementing the methodology is available via https://github.com/haydenmoffat/sequential_design_for_predator_prey_experiments.

Indexed as

Predatory BehaviorResearch DesignAnimalsComputer SimulationModels, BiologicalMonte Carlo MethodPopulation Dynamicsmodel discriminationmutual informationoptimal experimental designsequential Monte Carlototal entropy

Identifiers

PMID32396811
PMCPMC7276534

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.