scholarly journals Variety is the Spice of Life Histories: Comparison of Intraspecific Variability in Marine Invertebrates

2010 ◽  
Vol 50 (4) ◽  
pp. 630-642 ◽  
Author(s):  
M. W. Jacobs ◽  
R. D. Podolsky
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.


Abiotic variables and biotic interactions can act on variation in life history traits, ultimately leading to divergence in reproductive mode. Marine invertebrates have a remarkable diversity in such strategies, sometimes even between closely related species. It is this natural diversity that lends itself to employing a powerful comparative approach, both for particular morphological characteristics as well as molecular signatures from developmental genes. For example, complex life histories, where a larval stage is interposed between the embryo and juvenile, likely represent the product of numerous selection pressures, historical and current, that have shaped the diversity of larval stages in extant marine species. In fact, the very question about “what is a larva?” has to be addressed, as it is so intimately connected to bentho-planktonic life cycle and metamorphosis. Furthermore, novel larval types have evolved in particular lineages and larvae have been secondarily lost in others. This in itself creates an interesting and exciting playground to test evolutionary developmental hypotheses....


2013 ◽  
Vol 91 (1) ◽  
pp. 17-24 ◽  
Author(s):  
T.J. Oravec ◽  
T.E. Reimchen

To assess intraspecific variability in fecundity of threespine stickleback (Gasterosteus aculeatus L., 1758) as a test of life-history trade-offs, we quantified egg traits, morphological characters, and habitat variables in 43 allopatric and morphologically diverse populations from Haida Gwaii off the west coast of Canada. Mean mature egg size and total egg count (12 eggs per female and 8 gravid females per locality) were both positively and significantly correlated with standard length (SL) of the fish (r = 0.58 and 0.84, respectively). Egg size was ∼10% larger in freshwater localities than in similar-sized stickleback in adjacent marine localities (P < 0.02). Multiple regression and Akaike’s information criterion (AIC) analyses of residual egg size against morphological and lake habitat variables yields a negative correlation with lake pH (partial r = –0.34, P < 0.05) and no association with lake size, aquatic spectra, gill raker number, defense armor, or predation regime. Relative to stickleback from continental regions, Haida Gwaii stickleback life histories appear to be K-shifted (large but few eggs) possibly because of cool temperatures, low aquatic productivity, low community diversity, predation regime, and occasional iteroparity.


Paleobiology ◽  
1987 ◽  
Vol 13 (2) ◽  
pp. 113-139 ◽  
Author(s):  
Steven M. Stanley ◽  
Xiangning Yang

We have calculated rates of evolution for 19 lineages of Neogene bivalves over time intervals ranging from 1 ma to 17 ma. Our morphometric comparisons are based on 24 variables, for which we have made more than 43,000 individual measurements normalized for shell size. We initially assessed evolutionary changes in shape for 19 early Pliocene (4 ma old) species of bivalves by comparing these forms to their closest living relatives, which in 12 cases have traditonally been assigned to the same species. To make our study unbiased and comprehensive, we included all species that met certain predetermined guidelines and that offered suitable fossil material for measurement. We compared early Pliocene and Recent populations using (1) all 24 variables treated separately, (2) multivariate distance (Mahalanobis' D), based on the full set of variables, and (3) eigenshapes for shell outlines. For these comparisons, we used as a yardstick the same measures of morphologic distance applied to pairs of geographically separated Recent populations that belong to eight of the living species to which the fossil populations were compared. As it turns out, with minor exceptions, the distribution of morphologic distances between 4 ma old and Recent populations resembled the distribution of distances between conspecific Recent populations.We calculated net rates of evolution separating pairs of populations that belong to single lineages. For all intervals of time, the distribution of differences between population means for individual variables is remarkably similar to a comparable distribution representing the comparison of pairs of conspecific Recent populations from separate geographic regions. Because morphologic differences between populations do not vary greatly with evolutionary time, measured “rates” of evolution, on the average, decrease with interval of measurement. Because these differences resemble intraspecific variability, however, the rates do not represent significant evolution. Evolution has followed a weak zigzag course, yielding only trivial net trends.The weak and reversible “trends” that we measured yield net rates averaging less than 10 millidarwins, which is much lower than most rates previously reported for marine invertebrates (average ~200 millidarwins for a 1 ma interval and ~60 millidarwins for a 10 ma interval). We attribute this disparity (1) to the fact that most previously published rates have been calculated when a significant amount of evolution was recognized in advance (often for a poorly documented lineage) and (2) to the fact that most measured variables have represented nothing more than some measure of body size. We conclude that shape, as opposed to size, has been highly stable in bivalve evolution over millions of years and 106–107 generations. We conclude that to characterize rates or evolution for any group of organisms, one must employ a large, unbiased sample of measurements for numerous well-documented lineages, and one must segregate data depicting shape from data depicting size.


Developmental plasticity during the early life histories of marine invertebrates is a fascinating opportunity to study the interplay between ecology and evolution. In particular, some embryos and larvae initiate asexual reproduction while completing their development. This chapter examines the mode, frequency, and taxonomic diversity of asexual reproduction that occurs between the zygotic and the juvenile stages. Special attention is given to the phylum Echinodermata, where asexual reproduction during embryonic and larval development has been best studied. An emphasis is also placed on the factors that have been identified as likely inducers of asexual reproduction and an assessment of the likelihood that asexual reproduction is an adaptive response to these factors. Lastly, several key open questions are identified as potential avenues for future research about the causes and consequences of asexual reproduction by the developmental stages of marine invertebrates.


PeerJ ◽  
2019 ◽  
Vol 7 ◽  
pp. e6151 ◽  
Author(s):  
Daniel Doherty-Weason ◽  
Fernanda X. Oyarzun ◽  
Luciano Vera ◽  
Miguel Bascur ◽  
Fabián Guzmán ◽  
...  

In marine invertebrates, the modes of development at early stages are related to the type and capacity of larval feeding to achieve growth. Therefore, studying the factors that determine larval feeding strategies can help to understand the diversity of life histories and evolution of marine invertebrates. The polychaete Boccardia wellingtonensis is a poecilogonous species that encapsulates and incubates its offspring. This species produces two types of larvae: (1) larvae that do not feed within the capsule and hatch as planktotrophic larvae (indirect development), and (2) adelphophagic larvae that feed on nurse eggs and other larvae inside the capsule to hatch as advanced larvae or juveniles (direct development). Otherwise, the larval types are indistinguishable at the same stage of development. The non-apparent morphological differences between both types of larvae suggest that other factors are influencing their feeding behavior. This work studied the potential role of the activity of 19 digestive enzymes on the different feeding capacities of planktotrophic and adelphophagic larvae of B. wellingtonensis. Also, differences in larval feeding structures and the larval capacity to feed from intracapsular fluid were evaluated by electron and fluorescence microscopy. Results showed that both types of larvae present similar feeding structures and had the capacity to ingest intracapsular fluid protein. Adelphophagic larvae showed overall the highest activities of digestive enzymes. Significant differences between larval types were observed in nine enzymes related to the use of internal and external nutritional sources. Given that larval feeding is closely related to larval development in species with encapsulation, this work supports that the study of the digestive enzymatic machinery of larvae may contribute to understanding the evolution of developmental modes.


Diversity ◽  
2018 ◽  
Vol 11 (1) ◽  
pp. 2 ◽  
Author(s):  
Rachel Collin ◽  
Dagoberto Venera-Pontón ◽  
Amy Driskell ◽  
Kenneth Macdonald ◽  
Michael Boyle

Lingulids and discinids are the only brachiopods that exhibit life histories that include a feeding planktonic stage usually referred to as a “larva”. We collected planktotrophic brachiopod larvae from the Pacific and Caribbean coasts of Panama and took a DNA barcoding approach with mitochondrial cytochrome c oxidase subunit I (COI), mitochondrial ribosomal 16S, and nuclear ribosomal 18S genes to identify those larvae and to estimate their diversity in the region. We observed specimens from both coasts with distinct morphologies typical of lingulid and discinid larvae. COI and 16S were sequenced successfully for the lingulid larvae but failed consistently for all discinid larvae. 18S was sequenced successfully for larvae from both families. Sequence data from each gene revealed one lingulid operational taxonomic unit (OTU) from Bocas del Toro on the Caribbean coast, and one lingulid OTU from the Bay of Panama on the Pacific coast. These OTUs differed by >20% for COI, >10% for 16S and ~0.5% for 18S. Both OTUs clustered with GenBank sequences of Glottidia species, the only genus of lingulids in the Americas, but were distinct from G. pyramidata the only species reported for the Caribbean. Analysis of 18S sequence data for discinid larvae recovered 2 OTUs, one exclusively from the Pacific and one with a mixture of Pacific and Caribbean larvae. The 18S marker does not provide enough resolution to distinguish between species, and comparisons with GenBank sequences suggest that one OTU includes Pelagodiscus species, while the other may include Discradisca species. When compared with other marine invertebrates, our surveys of brachiopod larvae through DNA barcoding show relatively low levels of diversity for Panama.


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