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The evolutionary significance of egg size in marine invertebrates is commonly perceived in energetic terms. Embryonic size should also have direct effects upon the forces that govern swimming, a behavior common to early larval development in the plankton. If swimming is ecologically important, early larvae may need to perform to a certain 'standard', or threshold of speed and/or stability. The existence of performance standards in early development could therefore act to constrain the evolution of egg size and the evolution of development. Here we present the key parameters that characterize the upward swimming speed of ciliated spheroidal larvae moving at very low Reynolds numbers. The dependence of maximum supported mass upon larval size, and the independence of neutral-weight swimming speed from size, lead to hypotheses about scaling of swimming speed with size. Experimental studies with thirteen broadcastspawning planktotrophs demonstrate that flee-living embryonic swimmers in all of these species conform to a strong negative scaling of density with size that offsets increases in mass with increasing size. This trend suggests that swimming ability is broadly under selection in early development. In experimental studies and in a hydrodynamic model of larval swimming, the performance of trochophore larvae provides support for our hypothesized scaling relationships, and also for the concept of a standard in swimming speed. Echinoid blastulae, however, show relationships between speed and size that are not predicted by our scaling arguments. Results for echinoids suggest that differences in ciliary tip speed, or possibly in spatial density of cilia over the blastula's surface, result in significant differences in species' performance. Strong phyletic differences in the initial patterning and growth of structures used for swimming thus appear to cause significant differences in the relationship of swimming ability with embryo size. doi: 10.1093/icb/icq090

Compromises between swimming and feeding affect larval form and behavior. Two hypotheses, with supporting examples, illustrate these feeding-swimming trade-offs. (1) Extension of ciliated bands into long loops increases maximum clearance rates in feeding but can decrease stability of swimming in shear flows. A hydromechanical model of swimming by ciliated bands on arms indicates that morphologies with high performance in swimming speed and weight-carrying ability in still water differ from morphologies conferring high stability to external disturbances such as shear flows. Instability includes movement across flow lines from upwelling to downwelling water in vertical shear. Thus a hypothesis for the high arm elevation angles of sea urchin larvae, which reduce speed in still water, is that they reduce a downward bias imposed by the vertical shear in turbulence. Observations of sea urchin larvae in vertical shear and comparisons among brittle star larvae arc consistent with the performance trade-offs predicted by the model. (2) Structures and behaviors that reduce swimming speed can enhance filtering for feeding. In the opposed-band feeding mechanisms of veligers and many trochophores, cilia push water to swim but movement of cilia relative to the water occurs when cilia overtake and capture particles. Features that may increase clearance rates at the expense of speed and weight capacity include structures that increase drag or body weight and ciliary band that beats in opposition to the feeding-swimming current. Larval feeding mechanisms inherited from distant ancestors result in different swimming-feeding trade-offs. The different trade-offs further diversify larval form and behavior