Early metamorphosis is costly and avoided by young, but physiologically competent, marine larvae

2016 ◽  
Vol 559 ◽  
pp. 117-129 ◽  
Author(s):  
B Mos ◽  
SA Dworjanyn
Keyword(s):  
2018 ◽  
pp. 151-178
Author(s):  
Richard R. Strathmann

Modes of development of marine crustaceans and other marine invertebrates include presence or absence of a larval stage, of larval feeding, and of maternal protection of offspring. These different developmental modes impose different compromises (trade-offs) between the number of offspring and their size or the extent of maternal protection. Crustaceans differ from many marine animals in not shedding eggs prior to fertilization, which eliminates the complication of selection on size of eggs as a target for sperm. Features shared with marine invertebrates of several phyla include rare and ancient origins of feeding larvae, irreversible losses of a feeding larval stage, a constraint on brooding imposed by embryos’ need for oxygen, and possible benefits from slower development of protected embryos. Crustaceans differ, however, in having a diverse exoskeletal tool kit that has provided unusual capabilities. Nauplii and zoeae are diverse in form, behavior, and habitat, despite each being nominally one type of larva. Nauplii, as feeding larvae, have adapted to both the benthos and plankton. Settling stages (cyprids and decapodids) with enhanced speed have evolved twice. Some very large adults can supply their large broods with oxygen. Capacity for defense of offspring and home has led a few times to eusociality. The need to molt to grow and change form imposes episodic risk and growth and, in some cases, links evolution of egg size and size at metamorphosis. Crustaceans’ diverse life histories enable comparisons with broad implications for marine invertebrates: opportunity for dispersal is similar for larvae and adults of some crustaceans, demonstrating that marine larvae need not be adaptations for dispersal; development from very small eggs is enabled by less equipment needed for first larval feeding and also by postlarval stages being parasites; eggs shed into the water suffer greater mortality than planktonic larvae or brooded eggs, yet some planktonic crustaceans depend on benthic resting eggs for persistence of populations; larvae escape predation in diverse ways, and bigger larvae are not consistently safer; predation near the seafloor makes settlement a risky stage. Parallels with other taxa are numerous, but the crustacean exoskeletal tool kit has conferred unusual evolutionary opportunities and constraints. Even among marine crustaceans, however, evolutionary options for life histories differ among clades because of rare evolutionary origins of traits of larvae and mothers and biased evolutionary transitions in those traits.


1990 ◽  
Vol 15 (4) ◽  
pp. 427-437 ◽  
Author(s):  
PETER T. RAIMONDI ◽  
MICHAEL J. KEOUGH
Keyword(s):  

Aquaculture ◽  
1999 ◽  
Vol 177 (1-4) ◽  
pp. 333-343 ◽  
Author(s):  
Jorunn Skjermo ◽  
Olav Vadstein

2014 ◽  
Author(s):  
Lindsay D Waldrop ◽  
Roxanne M Bantay ◽  
Quang V Nguyen

Although many lineages of terrestrialized crustaceans have poor olfactory capabilities, crabs in the family Coenobitidae, including the terrestrial hermit crabs in the genus Coenobita, are able to locate food and water using olfactory antennae (antennules) to capture odors from the surrounding air. Terrestrial hermit crabs begin their lives as small marine larvae and must find a suitable place to undergo metamorphosis into a juvenile form, which initiates their transition to land. Juveniles increase in size by more than an order of magnitude to reach adult size. Since odor capture is a process heavily dependent on the size and speed of the antennules and physical properties of the fluid, both the transition from water to air and the large increase in size during ontogeny could impact odor capture. In this study, we examine two species of terrestrial hermit crabs, Coenobita perlatus H. Milne-Edwards and Coenobita rugosus H. Milne-Edwards, to determine how the antennule morphometrics and kinematics of flicking change in comparison to body size during ontogeny, and how this scaling relationship could impact odor capture by using a simple model of mass transport in flow. Many features of the antennules, including the chemosensory sensilla, scaled allometrically with carapace width and increased slower than expected by isometry, resulting in relatively larger antennules on juvenile animals. Flicking speed scaled as expected with isometry. Our mass-transport model showed that allometric scaling of antennule morphometrics and kinematics leads to thinner boundary layers of attached fluid around the antennule during flicking and higher odorant capture rates as compared to antennules which scaled isometrically. There were no significant differences in morphometric or kinematic measurements between the two species.


Marine larvae vary enormously in the amount of care (be it in the form of energy or other costly caregiving that increases offspring fitness) they receive from their parents. In contrast to terrestrial taxa, parental investment is less coupled to phylogeny in marine taxa, such that closely related species may have wildly different parental investment strategies. Such diversity demands explanation, and marine biologists have been fascinated by variation in parental investment for over 100 years. In this chapter, we review patterns in parental investment in space, review the theory of parental investment in life history theory, explore the key assumptions of life history theory as it pertains to parental investment, and then examine the evolutionary causes and ecological consequences of variation in parental investment for marine organisms.


2009 ◽  
Vol 7 (9) ◽  
pp. 664-672 ◽  
Author(s):  
Jean-Olivier Irisson ◽  
Cédric Guigand ◽  
Claire B. Paris

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