Osmoregulation in Larvae of the Land-Crab, Cardisoma guanhumi Latreille

Daily studies were made of the osmoregulatory abilities of Cardisomaguanhumi from hatching to the end of larval development. Theseresults were compared to those of similar research on osmoregulationby larvae and megalopa of four species of estuarine, littoral,and sub-littoral crabs. The comparison shows that larvae ofC. guanhumi possess the same kinds of adaptations for waterintake at the time of molt that were found in Rhithropanopeusharrisii. Land-crab larvae hyperregulated in 10 p.p.t. sea waterand hyporegulated in water of 40 p.p.t. for experimental periodsfor 2 hr during the first one-third of their development. Duringthe remainder of larval life, they hyporegulated against 15p.p.t. in intermolt periods and became isosmotic with, or hyporegulatedagainst, 10 p.p.t. at the time of molting. From the time ofhatching, the osmoregulatory pattern of developing C. guanhumifits them for deep penetration of estuaries and for crossingsteep saline gradients. This pattern is evidence for a strongerand more enduring control of water balance, especially at thetime of molting, than we have found in non-terrestrial species.     

The Effect of Environmental Factors on Development of the Land-Grab, Cardisoma guanhumi Latreille

Larvae of the land-crab, Cardisoma guanhumi, Latreille. weremaintained in 24 different combinations of salinity and temperaturefrom the time of hatching. Survival to the first crab occurredin salinities of 15–45 p.p.t., 25° and 30°C. Durationof the five zoeal and one megalops stages was similar in salinitiesof 20–40 p.p.t., but at 15 and 45 p.p.t. a greater periodof time was required for total development. Mortality of allthe larvae at 20°C suggests that temperature plays a moreimportant role in survival and distribution of the larvae ofC. guanhumi than salinity. Increments of size in crabs during the first seven post-larvalmolts were similar in salinities of 5–35 p.p.t., 25°C,but in fresh water increase in size at the time of molting wasreduced. Although there was no apparent relationship betweenfrequency of molting and salinities of 5–35 p.p.t., theduration of intermolt was reduced in crabs maintained in freshwater, and survival was also lower. From the present study there is no indication that the morphologicaland physiological processes that are associated with adaptationof the adult crab to the terrestrial environment are initiatedduring larval development. Although the adult crabs have successfullypenetrated the terrestrial environment, the pelagic larvae arestill subject to the numerous ecological variables of the estuarineand marine environments.     

The Ontogeny of Osmoregulation and Its Neurosecretory Control In the Decapod Crustacean, Rhithropanopeus harrisii (Gould)

Laboratory-hatched larvae of this estuarine crab were rearedat 25°C in seawater of 25 salinity for 18 days coveringzoeal Stages I to IV and a megalops. Three-day periods betweenzoeal stages represent intermolt stages of circadean metecdysis,diecdysis, and proecdysis.Larvae were exposed to either a seriesof seawater salinities from 5-40 in 5 increments or of 10-40in 10 increments for one hour during each day of their development.The osmoconcentrations of 20-80 nanoliter hemolymph samplesfrom each of four larvae were measured separately by determinationsof freezing point depression. Eyestalkless larvae in metecdysis of zoeal Stage II were exposedto the same osmoconcentrations as unoperated controls to testfor osmoregulation by eyestalk nerve tissue. Larvae tend to be isosmotic with seawater of 30-40 salinity(S) and to hyperregulate in more dilute media except for larvaein their first diecdysis which remain isosmotic. Larvae in thelast few hours of proecdysis hyperregulate against 40 S as well,presumably to insure inflow of water to establish a greaterbody volume during hardening of the exoskeleton. They are consequentlyisosmotic in the very early metecdysis. The presence of eyestalks at the first metecdysis (Stage II)keeps zoeas hyperosmotic to 5-30 S, but prevents them from hyperregulationagainst 40 S. Eyestalkless zoeas become isosmotic with 5-30S and hyperregulate against 40 S like late proecdysal larvae.Lack of eyestalks makes diecdysal animals hyperregulate againsta medium with which normal animals are isosmotic. The eyestalkinfluence affects second metecdysal (Stage III) larvae in away similar to those in first metecdysis except that it apparentlyalso prevents a curious tendency to hyporegulate in 5-30 S.Similarly, in this stage, the eyestalks prevent hyperosmosityin 40 S seawater as they do during the first day of zoeal StageII. Eyestalk nerve tissue reduces the degree to which diecdysallarvae of this stage remain hyperosmotic to media of 10 S and20 S and apparently causes larvae to be hypoosmotic at 40 S. Preliminary data indicate that removal of eyestalks has littleeffect on proecdysal larval osmoregulation or on regulationof Stage IV zoeas. In other experiments ablation of eyestalks caused Stage II larvaeto lose the ability to osmoregulate against 10-30 S seawaterwithin two hours after the operation. The same zoeas did nothyperregulate against 40 seawater until four hours after removalof eyestalks.