Egg-size manipulations in the seed beetle Stator limbatus: consequences for progeny growth

1997 ◽  
Vol 75 (9) ◽  
pp. 1465-1473 ◽  
Author(s):  
Charles W. Fox

Studies that have demonstrated consequences of variation in egg size for progeny growth and development are often confounded by genetic correlations among life-history characters; relationships between egg size and progeny life-history characters do not always reflect cause and effect. Thus, experimental approaches to manipulating egg size in order to quantify the consequences of egg-size variation for progeny growth and development have been developed. I used egg-size plasticity in response to oviposition environment to manipulate egg size in a seed beetle, Stator limbatus, to test the hypothesis that progeny developing from larger eggs survive better, develop faster, and attain a larger adult body size than progeny developing from smaller eggs. Females exposed to Cercidium floridum during egg maturation laid eggs that were substantially larger than those laid by females exposed to Acacia greggii during egg maturation. The larger eggs laid by females exposed to C. floridum took significantly longer to hatch but had shorter total egg-to-adult development times than eggs laid by females exposed to A. greggii (when reared to adulthood on A. greggii). There was no evidence from the between-treatment comparisons that egg size affected egg-to-adult survivorship or the size at which progeny emerged as adults. Within-treatment correlations between egg size and progeny life-history characters were generally consistent with the between-treatment analyses, except that female progeny developing from larger eggs tended to emerge as larger adults than female progeny developing from smaller eggs. This result is interpreted as a consequence of heritable variation in body size rather than a cause-and-effect relationship between egg size and progeny body size.

Parasitology ◽  
2011 ◽  
Vol 138 (7) ◽  
pp. 848-857 ◽  
Author(s):  
G. LOOT ◽  
N. POULET ◽  
S. BROSSE ◽  
L. TUDESQUE ◽  
F. THOMAS ◽  
...  

SUMMARYObjective. Unravelling the determinants of parasite life-history traits in natural settings is complex. Here, we deciphered the relationships between biotic, abiotic factors and the variation in 4 life-history traits (body size, egg presence, egg number and egg size) in the fish ectoparasite Tracheliastes polycolpus. We then determined the factors affecting the strength of the trade-off between egg number and egg size. Methods. To do so, we used 4-level (parasite, microhabitat, host and environment) hierarchical models coupled to a field database. Results. Variation in life-history traits was mostly due to individual characteristics measured at the parasite level. At the microhabitat level (fins of fish hosts), parasite number was positively related to body size, egg presence and egg number. Higher parasite number on fins was positively associated with individual parasite fitness. At the host level, host body size was positively related to the individual fitness of the parasite; parasites were bigger and more fecund on bigger hosts. In contrast, factors measured at the environmental level had a weak influence on life-history traits. Finally, a site-dependent trade-off between egg number and egg size existed in this population. Conclusion. Our study illustrates the importance of considering parasite life-history traits in a hierarchical framework to decipher complex links between biotic, abiotic factors and parasite life-history traits.


1990 ◽  
Vol 68 (1) ◽  
pp. 44-48 ◽  
Author(s):  
Larry D. Marshall

Daily egg production of the moth Parapediasia teterrella declined over the life-span of the female but egg size remained constant. The absence of water resulted in lower fecundity and early mortality. Egg size and lifetime fecundity showed considerable inter-individual variation and large females produced more and larger eggs than their smaller counterparts. Large females expended greater reproductive effort than small females. Hatching success was negatively related to egg size. In spite of this, large females laying large eggs had higher fitness than small females. I postulate that multiple reproductive strategies within a species, resulting from differences in reproductive effort expended, may explain why expected trade-offs in reproductive parameters (e.g., egg size versus egg number) were not found in this species. Furthermore, I argue that the prevalent interpretation of life-history evolution (that body size is the important determining parameter of life-history parameters) may reflect correlation of body size with reproductive effort, and reproductive effort may be more important in determining the nature of trade-offs between reproductive parameters.


2019 ◽  
Author(s):  
WU Blanckenhorn ◽  
V Llaurens ◽  
C Reim ◽  
Y Teuschl ◽  
E Postma

SUMMARYThe evolutionary potential of organisms depends on the presence of sufficient genetic variation for traits subject to selection, as well as on the genetic covariances among them. While genetic variation ultimately derives from mutation, theory predicts the depletion of genetic (co)variation under consistent directional or stabilizing selection in natural populations. We estimated and compared additive genetic (co)variances for several standard life history traits, including some for which this has never been assessed, before and after 24 generations of artificial selection on male size in the yellow dung fly Scathophaga stercoraria (Diptera: Scathophagidae) using a series of standard half-sib breeding experiments. As predicted, genetic variances (VA), heritabilities (h2) and evolvabilities (IA) of body size, development time, first clutch size, and female age at first clutch were lower after selection. As independent selection lines were crossed prior to testing, we can rule out that this reduction is due to genetic drift. In contrast to the variances, and against expectation, the additive genetic correlations between the sexes for development time and body size remained strong and positive (rA = 0.8–0.9), while the genetic correlation between these traits within the sexes tended to strengthen (but not significantly so). Our study documents that the effect of selection on genetic variance is predictable, whereas that on genetic correlations is not.


Parasitology ◽  
1997 ◽  
Vol 114 (2) ◽  
pp. 195-204 ◽  
Author(s):  
R. POULIN

Parasite life-history traits should reflect past environmental and host-related selective pressures acting to produce strategies that maximize transmission success. The evolution of adult body size and egg production in 804 species of trematode parasites was investigated using independent contrasts derived from a phylogeny of trematodes. Contrasts in trematode body size were positively correlated with contrasts in egg size, and almost significantly correlated with contrasts in numbers of uterine eggs. After controlling for body size, no relationship existed between egg size and egg numbers, suggesting that there is no trade-off between the two components of egg production. Average host body mass and latitude of the sampling site did not correlate with either trematode body size or egg size. Contrasts between trematode taxa exploiting ectotherm hosts and their sister taxa exploiting endotherms showed no consistent difference in either body size or egg size. The effect of other variables on trematode life-histories, such as the nature of the habitat in which eggs are released, the site of attachment within the host's body, or the number of hosts involved in the life-cycle, could not be evaluated statistically. The similarity in life-history traits among members of given clades suggests that phylogenetic constraints may have acted to limit or mask any adaptive changes expected from changes in host-related or environmental conditions.


2002 ◽  
Vol 62 (2) ◽  
pp. 321-332 ◽  
Author(s):  
D. RODRIGUES ◽  
G. R. P. MOREIRA

Adult body size, one of the most important life-history components, varies strongly within and between Heliconius erato phyllis (Lepidoptera: Nymphalidae) populations. This study determines if this variation is caused by geographical changes in host-plant used by the larval stage, whose reproductive parameters are influenced by female body size, with estimates of the corresponding heritability. The variation in adult body size was determined together with a survey of passion vine species (Passifloraceae) used by the larvae in seven localities in Rio Grande do Sul State: three located in the urban area of Porto Alegre and Triunfo Counties, two within Eucalyptus plantations (Barba Negra Forest, Barra do Ribeiro County, and Águas Belas Experimental Station -- Viamão County), one in a Myrtaceae Forest (Itapuã State Park -- Itapuã County) and one in the Atlantic Rain Forest (Maquiné Experimental Station -- Maquiné County). Effects of female body size on fecundity, egg size and egg viability were determined in an outdoor insectary. Size heritability was estimated by rearing in the laboratory offspring of individuals maintained in an insectary. The data showed that adults from populations where larvae feed only upon Passiflora suberosa are smaller than those that feed on Passiflora misera. The larvae prefer P. misera even when the dominant passion vine in a given place is P. suberosa. Fecundity increases linearly with the increase in size of females, but there is no size effect on egg size or viability. Size heritability is null for the adult size range occurring in the field. Thus, the geographical variation of H. erato phyllis adult size is primarily determined by the type, corresponding availability and quality of host-plants used by the larval stage. Within the natural size range of H. erato phyllis, the variation related to this caracter is not genetically based, thus being part of H. erato phyllis phenotypic plasticity.


Author(s):  
J.G. Greenwood ◽  
M.B. Jones ◽  
J. Greenwood

Surprisingly little is known about the influence of salinity on embryo development in crustaceans despite its obvious potential importance to species which breed in inshore estuarine waters. Evidence from the literature is that embryo salinity tolerance may differ from that of later stages in the life history (e.g. Kelley & Burbanck, 1976; Rosenberg & Costlow, 1979; Hartnoll & Paul, 1982; Jones & Simons, 1982; Wear et al., 1986) and such differences may impose restrictions on distribution. Wittmann (1984) referring to mysids, emphasised that an understanding of incubation period and factors influencing it "appears to be a key factor for the understanding of variations in the length and timing of the breeding season, age of maturity, frequency of broods, numbers of young per brood, egg size, and adult body size".


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