Abstract
Average filtration and growth rates of groups of juvenile Mytilus edulis (n=25–45 of 22–35 mm shell length) were measured at different concentrations of an algal cell monoculture in 9 laboratory experiments of duration 14–30 days, 4 experiments below and 5 above the limit of incipient saturation concentration (C sat≈6000–7000 Rhodomonas salina cells ml−1). From a nearly constant filtration rate (F≈30 ml min−1 for a 30 mm shell length) at measured algal concentrations below C sat the steady-state filtration rate decreased approximately as 1/C for increasing algal concentrations (C) above C sat to levels as low as 12–9% of the former value. Corresponding calculated gross ingestion rates (I=F×C) increased linearly below C sat and remained nearly constant above C sat. However, the measured weight-specific growth rates (µ) decreased sharply above C sat from a maximal value of about 9.5% day−1 to about 1.5% day−1. Below C sat on the other hand, measured µ values increased linearly with increasing algal concentration, which was in good agreement with an earlier advanced bioenergetic growth model. The overall functional response of M. edulis resembles a Type I in terms of gross ingestion, but with a rapid decrease instead of a constant above C sat in terms of actual ingestion and growth. The physiological implications of the functional response remain uncertain. The response to increasing food concentration with possible regulation of net ingestion appears only to come into play when C sat is exceeded and then as partial valve closure and reduced filtration and growth rates along with production of pseudofaeces. A survey of naturally occurring phytoplankton biomass in the sea shows that this is generally below C sat except for the short spring bloom periods; hence, mussels generally feed at optimal rates depending on the composition and concentration of biomass exceeding the minimal concentration below which the mussels close their valves and reduce or cease filtering.
Published in collaboration with the Institute of Marine Research, Norway
Published in collaboration with the Institute of Marine Research, Norway
Acknowledgements
This work formed part of the MarBioShell project supported by the Danish Agency for Science, Technology and Innovation for the period January 2008 to December 2012. Thanks are due to Isabel Barreiro Saavedra for technical assistance and to the Danish Nature Agency, Danish Ministry of the Environment, for providing chlorophyll a concentrations.
Notes
Published in collaboration with the Institute of Marine Research, Norway