Patterns in stage duration and development among marine and freshwater calanoid and cyclopoid copepods: a review of rules,physiological constraints,and evolutionary significance

Studies of development time of marine and freshwater copepods have taken separate tracks. Most studies on marine copepods report development time of each individual development stage, whereas studies on freshwater copepods report only development time, from egg to nauplius and nauplius to adult. This bias allows comparison of total development time but prevents detailed comparisons of patterns in stage-specific developmental schedules. With respect to egg to adult development time, three general relationships are known: developmental rates are dependent upon temperature and food concentration but independent of terminal body size; freshwater calanoids develop significantly slower than marine calanoids; freshwater cyclopoids develop at the same rate as marine calanoids. Two rules describe stage-specific developmental rates: the equiproportional rule and the isochronal rule. The first rule states that the duration of a given life history stage is a constant proportion of the embryonic development time; the second rule states that the time spent in each stage is the same for all stages. This review focuses on the second rule. From the 80+ published studies of copepod stage-specific developmental times, no species follows the isochronal rule strictly: Acartia spp. come closest with isochronal development from third nauplius (N3) to fourth copepodite (C4). The only pattern followed by all species is rapid development of the first and/or second naupliar stages, slow development of the second and/or third nauplius and prolonged development of the final copepodite stage. Once adulthood is reached, males are usually short-lived, but females can live for weeks to months in the laboratory. Adult longevity in the sea is, however, on the order of only a few days. The evolution of developmental patterns is discussed in the context of physiological constraints, along with consideration of possible relationships between stage-specific mortality rates and life history strategies. Physiological constraints may operate at critical bottlenecks in development (e.g. at the first feeding nauplius, N6, and the fifth copepodite stage). High mortality of eggs may explain why broadcast eggs hatch 2–3 times faster than eggs carried by females in a sac; high mortality of adults may explain why adults do not grow rather they maximize their reproductive effort by partitioning all energy for growth into egg production.