Symbiosis increases population size and buffers environmental fluctuations in a physiologically-structured model parameterized for thyasirid bivalves

Symbioses whereby one partner provisions a nutritional resource to the other may alter energy allocation towards reproduction and survival in the recipient partner, potentially impacting population dynamics. Asymbiotic thyasirid bivalves feed predominantly on free-living bacteria, which fluctuate in abundance due to seasonality-driven temperature variations. Symbiotic thyasirids are mixotrophs, gaining nutrients from free-living bacteria and symbiotic bacteria that they host on their enlarged gills. Symbiotic bacteria may function as an additional energy reserve for thyasirids, allowing the hosts to allocate more energy to reproduction. We hypothesize that, for symbiotic thyasirids, the symbionts are a nutritional source that mitigates resource limitation. Using Dynamic Energy Budget theory, we built a physiologically-structured population model assuming equal mortality rates in both species. We find that without seasonal fluctuations, symbiotic thyasirids have higher abundances than asymbiotic thyasirids since the symbionts increase reproduction. Both species have similar population sizes in fluctuating environments, suggesting different adaptations to seasonality: asymbiotic thyasirids have adapted their physiology, while symbiotic thyasirids have adapted through mixotrophy. Our results highlight the significance of linking individual energetics and life-history traits to population dynamics and are the first step towards understanding the role of symbioses in population and community dynamics.

A Dynamic Energy Budget Model of Ornate Box Turtle Shell Growth

Many aspects of box turtle development may depend on size rather than age. Notable examples include sexual maturity and the development of the fully closing hinge in the shell that allows box turtles to completely hide in their shells. Thus, it is important to understand how turtles grow in order to have a complete understanding of turtle biology. Previous studies show that turtle shell growth behaves in a logistic manner. These studies use functional models that fit the data well but do little to explain mechanisms. In this work we use the ideas found in dynamic energy budget theory to build a model of box turtle shell growth. We show this model fits the data as well as previous models for ornate box turtles Terrapene ornata ornata, but also offers explanations for observed phenomena, such as maximum sizes and the appearance of biphasic growth.