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Newly hatched artemia nauplii. the mixture of food types and sizes accommodated the nutritional needs of all larval stages. treatment dishes were examined daily and data on mortality and molting were recorded. molts and dead larvae were noted and removed from the treatment dishes. during the first three years, larvae from northern california were raised and monitored in groups of 10 individuals within a glass culture dish 100 ml ; , with each group of 10 larvae constituting a replicate. mortality and development time to megalopae and juvenile crab stage were recorded. during the last 2 years, larvae were raised and monitored individually in polystyrene parts boxes 20 ml water per compartment ; , allowing us to record development and survivorship for each zoeal stage as individuals. in both cases, larvae that reached the megalopae stage were separated from the developing zoea and placed in larger containers 40 ml water ; , provided more food and given a piece of nitex mesh upon which to settle. the water volume and food was again increased 80 ml, and pieces of shrimp or squid were added ; for juvenile crabs. salinity tolerance experiments: full factorial experiments for temperature x salinity were conducted with larvae obtained from ovigerous crabs collected in bodega bay, ca table 1 ; . in 1999, theses experiments included all combinations of four temperatures 5, 15, 25, oc ; and four salinities 5, 10, 20, ppt ; . experiments run in 2000 tested combinations of four low temperatures 5, 7.5, 10, oc ; and the two high salinities 20, 30 ppt ; . for each treatment combination, we tested three replicate groups of 10 larvae hatched from of each of 3-5 broods, such that there were 9-15 groups tested at each temperature x salinity combination. table 1: salinity experiments 1999 and 2000. 1999 salinity 2000 salinity temp 5 10 20 temp 20 30 x 5.0 x x x 15.0 7.5 x x x 25.0 10.0 x x x 30.0 12.5 constant temperature tolerance experiments: temperature tolerance experiments were conducted seasonally over a five year period using larvae obtained from ovigerous female crabs collected from two invasive populations: california all years ; and maine year 2002 only ; table 2 ; . experiments in the first year 1999 ; focused on salinity treatments and high and low extreme temperatures. the second year 2000 ; focused on lower temperatures and higher salinities. the third year 2001 ; tested not only the effect of exposure temperature on the larvae, but also the effect of acclimation temperature of the ovigerous females. in the fourth year 2002 ; , larval development at relatively mid to high temperatures was compared between source populations of crabs from northern california and maine. in the fifth year 2003 ; california larvae were raised at cold temperatures to test for a potential lower threshold of development. for each treatment combination during 1999-2001, we tested three replicate groups of 10 larvae hatched from of each of 3-5 broods, such that there. 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