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Relationship: 2938
Title
Decreased, Viable Offspring leads to Decrease, Population growth rate
Upstream event
Downstream event
Key Event Relationship Overview
AOPs Referencing Relationship
AOP Name | Adjacency | Weight of Evidence | Quantitative Understanding | Point of Contact | Author Status | OECD Status |
---|---|---|---|---|---|---|
PPARalpha Agonism Leading to Decreased Viable Offspring via Decreased 11-Ketotestosterone | adjacent | Moderate | Low | Arthur Author (send email) | Open for citation & comment |
Taxonomic Applicability
Term | Scientific Term | Evidence | Link |
---|---|---|---|
teleost fish | teleost fish | NCBI |
Sex Applicability
Sex | Evidence |
---|---|
Unspecific |
Life Stage Applicability
Term | Evidence |
---|---|
All life stages |
Key Event Relationship Description
Population growth rate which measures the per capita rate of population increase over a time interval is proportional to the instantaneous birth rate (number of births per individual per unit of time and the instantaneous death rate (number of deaths per individual per unit of time) (Caswell 2001, Miller and Ankley 2004, Gotelli 2008, Vandermeer and Goldberg 2013, Murray and Sandercock 2020). Decreases in viable offspring could therefore lead to decreased population growth rate, recognizing that other factors (e.g., immigration/emigration, intraspecific and interspecific competition, predation, disease) influence population growth. Population models could be employed to aide in understanding how changes to population growth rate result from various levels of decline in recruitment of young of year fish.
Evidence Collection Strategy
Evidence Supporting this KER
There is no empirical data suitable for evaluating the dose-response, temporal, or incidence concordance between a reduction in the number of viable offspring and decrease in population growth rate. However, population modeling/simulation approaches could be applied in investigating this KER.
Biological Plausibility
A decrease in population growth rate whereby the per capita rate of population change is negative over time can result from either a decline in the instantaneous birth rate and/or an increasein the instantaneous death rate (Caswell 2001, Miller and Ankley 2004, Gotelli 2008, Vandermeer and Goldberg 2013, Murray and Sandercock 2020). While the number of eggs produced by female fish would not be directly impacted, impaired spermatogenesis in male fish that results in decreased oocyte fertilization and/or a reduction in viable offspring would reduce the population growth rate over time as fewer eggs on average would survive to become young of year fish. Thus, the reproductive potential of female fish adjusted for the inability of fertilized eggs to progress and hatch into viable offspring would be expected to result in a decline in recruitment and contribution of offspring to the next generation (a decline in net reproductive rate) (Caswell 2001, Gotelli 2008, Vandermeer and Goldberg 2013).
Empirical Evidence
There is very limited empirical data for this KER; thus, evidence is based on biological plausibility and population models.
Uncertainties and Inconsistencies
There is limited empirical data for this KER. Population models are often parameterized based on information from a single species. Studies at the population level rely upon observation and estimation of a number of species-specific variables that influence population growth rate (e.g. age or stage specific estimates of survival and fecundity), each of which has an associated uncertainty. There are also uncertainties in extending the population model (extrapolation of model predictions) to be applicable to other species.
Known modulating factors
Quantitative Understanding of the Linkage
Response-response Relationship
Decreased oocyte fertilization and/or a reduction in viable offspring would result in reduced survival of eggs to become young of year fish. This in turn would result in a lower population growth rate over time.
Time-scale
The time-scale at which decrease in viable offspring would impact population levels is dependent on a species life cycle, with the potential for impacts in the short term (i.e. days or weeks) for short-lived species and much longer (years) for long-lived species.
Known Feedforward/Feedback loops influencing this KER
Domain of Applicability
References
Caswell H. 2001. Matrix Population Models. Sinauer Associates, Inc., Sunderland, MA, USA.
Galic N, Hommen U, Baveco JM, van den Brink PJ (2010) Potential application of population models in the European ecological risk assessment of chemicals. II. Review of models and their potential to address environmental protection aims. Integr Environ Assess Manag 6:338–360.
Gotelli NJ. 2008. A Primer of Ecology. Sinauer Associates, Inc., Sunderland, MA, USA.
Miller DH, Ankley GT. 2004. Modeling impacts on populations: Fathead minnow (Pimephales promelas) exposure to the endocrine disruptor 17b-trenbolone as a case study. Ecotox Environ Saf 59:1–9.
Mittelbach GG, McGill BJ (2019) Community ecology. Oxford University Press, Oxford.
Murray DL, Sandercock BK. 2020. Population ecology in practice. Wiley-Blackwell, Oxford UK, 448 pp.
Vandermeer JH, Goldberg DE. 2013. Population ecology: first principles. Princeton University Press, Princeton, NJ USA.