No abstract

SUMMARYBody temperatures and thus physiological rates of poikilothermic organisms are determined by environmental temperature. The power an organism has available for swimming is largely dependent on physiological rates and thus body temperature. However, retarding forces such as drag are contingent on the temperature-dependent physical properties of water and on an organism's size. Consequently, the swimming ability of poikilotherms is highly temperature dependent. The importance of the temperaturedependent physical properties of water (e.g. viscosity) in determining swimming speed is poorly understood. Here we propose a semi-mechanistic model to describe how biological rates, size and the physics of the environment contribute to the temperature dependency of microbial swimming speed. Data on the swimming speed and size of a predatory protist and its protist prey were collected and used to test our model. Data were collected by manipulating both the temperature and the viscosity (independently of temperature) of the organism's environment. Protists were either cultured in their test environment (for several generations) or rapidly exposed to their test environment to assess their ability to adapt or acclimate to treatments. Both biological rates and the physics of the environment were predicted to and observed to contribute to the swimming speed of protists. Body size was not temperature dependent, and protists expressed some ability to acclimate to changes in either temperature or viscosity. Overall, using our parameter estimates and novel model, we are able to suggest that 30 to 40% (depending on species) of the response in swimming speed associated with a reduction in temperature from 20 to 5°C is due to viscosity. Because encounter rates between protist predators and their prey are determined by swimming speed, temperature-and viscosity-dependent swimming speeds are likely to result in temperature-and viscosity-dependent trophic interactions. Supplementary material available online at

Summary1. While much is known about the independent effects of trophic structure and temperature on density and ecosystem processes, less is known about the interaction(s) between the two. 2. We manipulated the temperature of laboratory-based bacteria-protist communities that contained communities with one, two, or three trophic levels, and recorded species' densities and bacterial decomposition. 3. Temperature, food chain length and their interaction produced significant responses in microbial density and bacterial decomposition. Prey and resource density expressed different patterns of temperature dependency during different phases of population dynamics. The addition of a predator altered the temperature-density relationship of prey, from a unimodal trend to a negative one. Bacterial decomposition was greatest in the presence of consumers at higher temperatures. 4. These results are qualitatively consistent with a recent model of direct and indirect temperature effects on resource-consumer population dynamics. Results highlight and reinforce the importance of indirect effects of temperature mediated through trophic interactions. Understanding and predicting the consequences of environmental change will require that indirect effects, trophic structure, and individual species' tolerances be incorporated into theory and models.

Summary1. While much is known about the direct effect that temperature can have on aquatic communities, less is known about its indirect effect via the temperature dependence of viscosity and temperaturedependent trophic interactions. 2. We manipulated the temperature (5-20°C) and the viscosity (equivalent to 5-20°C) of water in laboratory-based bacteria-protist communities. Communities contained food chains with one, two or three trophic levels. Responses measured were population dynamics (consumer carrying capacity and growth rate, average species population density, and the coefficient of variation of population density through time) and ecosystem function (decomposition). 3. Temperature, viscosity and food chain length produced significant responses in population dynamics. Temperature-dependent viscosity had a significant effect on the carrying capacity and growth rates of consumers, as well as the average density of the top predator. Overall, indirect effects of temperature via changes in viscosity were subtle in comparison to the indirect effect of temperature via trophic interactions. 4. Our results highlight the importance of direct and indirect effects of temperature, mediated through trophic interactions and physical changes in the environment, both for population dynamics and ecosystem processes. Future mechanistic modelling of effects of environmental change on species will benefit from distinguishing the different mechanisms of the overall effect of temperature.

In Melipona quadrifasciata, about 10% of the females develop into queens, almost all of which are killed. Occasionally, a new queen replaces or supersedes the mother queen or heads a new colony. We investigated virgin queen fate in queenright and queenless colonies to determine the effects of queen behaviour, body mass, nestmate or non-nestmate status, queenright or queenless colony status, and, when queenless, the effect of the time a colony had been queenless, on survival duration and acceptance. None of 220 virgin queens observed in four observation hives ever attacked another virgin queen nor did any of 88 virgin queens introduced into queenright colonies ever attack the resident queen. A new queen was only accepted in a queenless colony. Factors increasing survival duration and acceptance of virgin queens were to emerge from its cell at 2 h of queenlessness, to hide, and to avoid fights with workers. In this way, a virgin queen was more likely to be available when a colony chooses a new queen, 24-48 h after resident queen removal. Running, walking or resting, antennating or trophallaxis, played little or no role, as did the factors body mass or nestmate. "Queen choice" took about 2 h during which time other virgin queens were still being killed by workers. During this agitated process, the bees congregated around the new queen. She inflated her abdomen and some of the workers deposited a substance on internal nest surfaces including the glass lid of the observation hive.