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Fecundity Rates (fecundity + rate)
Selected AbstractsLife history of Littorina scutulata and L. plena, sibling gastropod species with planktotrophic larvaeINVERTEBRATE BIOLOGY, Issue 1 2002Paul A. Hohenlohe Abstract. The intertidal, sibling species Littorina scutulata and L. plena (Gastropoda, Proso-branchia) are sympatric throughout most of their ranges along the Pacific coast of North America. Both species release disc-shaped, planktonic egg capsules from which planktotrophic veliger larvae hatch. Here I review existing data and present new observations on these species' life history, including age at first reproduction, spawning season, maximum fecundity rates, capsule morphology, egg size and number, pre-hatching development, larval growth at three food concentrations, potential settlement cues, planktonic period, and protoconch size. Previous classification of egg capsule morphologies used to distinguish the species is inaccurate; instead, capsules can be categorized into three types of which each species may produce two. Females of L. scutulata produced capsules with either two rims of unequal diameter or one rim, while females of L. plena produced capsules with one rim or two rims of nearly equal diameter. Females of each species spawned sporadically from early spring to early fall in Puget Sound. Larvae of L. plena hatched one day earlier than those of L. scutulata, and both species grew fastest in the laboratory at intermediate food concentrations. Larvae metamorphosed in the presence of a variety of materials collected from their adult habitat, including conspecific adults, algae, rocks, and barnacle tests. This is the first report of planktotrophic larvae in this genus metamorphosing in the laboratory. The total planktonic period of 8 larvae of L. scutulata raised in the laboratory was 37,70 days, and a single larva of L. plena metamorphosed after 62 days. Protoconch diameter of shells collected from the field was 256,436 ,m and did not differ significantly between the species. Previous allozyme and mitochondrial DNA work has suggested high levels of genetic variability in both species and greater genetic population structure in L. plena, despite the long spawning season and long-lived larvae in both species. The interspecific life history differences described here appear insufficient to produce consistent differences in gene flow patterns. [source] Cohort variation in offspring growth and survival: prenatal and postnatal factors in a late-maturing viviparous snakeJOURNAL OF ANIMAL ECOLOGY, Issue 3 2010Jean-Pierre Baron Summary 1. Recruitment to adulthood plays an important role in the population dynamics of late-maturing organisms as it is usually variable. Compared to birds and mammals, few studies assessing the contributions to this variation of environmental factors, offspring traits and maternal traits have been carried out for late-maturing snakes. 2. Cohort variation in recruitment through offspring growth and survival in the meadow viper (Vipera ursinii ursinii) was evaluated from 13 years of mark,recapture data collected at Mont Ventoux, France. In this species, females are mature at the age of 4,6 years and adult survival and fecundity rates are high and constant over time. 3. Offspring were difficult to catch during the first 3 years of their lives, but their mean annual probability of survival was reasonably high (0·48 ± 0·11 SE). Mass and body condition at birth (mass residuals) varied significantly between years, decreased with litter size, and increased with maternal length. 4. Cohorts of offspring in better condition at birth grew faster, but offspring growth was not affected by sex, habitat or maternal traits. 5. Survival varied considerably between birth cohorts, some cohorts having a high-survival rate and others having essentially no survivors. No difference in mass or body condition at birth was found between cohorts with ,no survival' and ,good survival'. However, offspring survival in cohorts with good survival was positively correlated with mass at birth and negatively correlated with body condition at birth. 6. Thus, variation in offspring performance was influenced by direct environmental effects on survival and indirect environmental effects on growth, mediated by body condition at birth. Effects of maternal traits were entirely channelled through offspring traits. [source] Characterization of Oestrous Induction Response, Oestrous Duration, Fecundity and Fertility in Awassi Ewes During the Non-breeding Season Utilizing both CIDR and Intravaginal Sponge TreatmentsREPRODUCTION IN DOMESTIC ANIMALS, Issue 3 2010N Ozyurtlu Contents The aim of this study was to investigate characterization of oestrous response, onset of induced oestrus, oestrous duration, fecundity and fertility in Awassi ewes treatment with intravaginal sponges and Controlled Intravaginal Drug Release (CIDR) devices in combination with pregnant mare serum gonadotropin (PMSG) under local environmental conditions during the non-breeding season. A total of 62 ewes were divided into three groups. Group CIDR (n = 20) was treated with CIDR devices for 12 days and 400 IU PMSG was injected upon removal of the CIDR. For ewes in Group Sponge (SP) (n = 24), 30 mg fluorogestone acetate was administered to the sheep for 12 days and 400 IU PMSG was injected upon withdrawal of the sponge. Group Control (CON) (n = 18) served as a control group and received no treatment. Adult, intact and sexually experienced Awassi rams were introduced to all groups at the time when the intravaginal devices were removed. There were no significant differences in terms of oestrous response (CIDR: 90%, SP: 87.5%), time to onset of oestrus and duration of induced oestrus between the CIDR and SP groups. The oestrous response of treatment groups was significantly greater (p < 0.05) than in the control ewes. There were no significant differences in pregnancy (CIDR: 70%, SP: 70.8%), lambing (CIDR: 85%, SP: 79.2%) and fecundity rates between ewes treated with CIDR and those treated with sponges. However, pregnancy and lambing rates were significantly (p < 0.05) higher in ewes treated with CIDR or sponges when compared with those in the control group. It was concluded that it is possible to induce fertile oestrus, successful pregnancy and lambing with the treatment of either CIDR or intravaginal sponge in combination with PMSG in Awassi ewes during the non-breeding season. [source] Life history evolution in a globally invading tephritid: patterns of survival and reproduction in medflies from six world regionsBIOLOGICAL JOURNAL OF THE LINNEAN SOCIETY, Issue 1 2009ALEXANDROS D. DIAMANTIDIS Comparisons among populations from different localities represent an important tool in the study of evolution. Medflies have colonized many temperate and tropical areas all over the world during the last few centuries. In a common garden environment, we examined whether medfly populations obtained from six global regions [Africa (Kenya), Pacific (Hawaii), Central America (Guatemala), South America (Brazil), Extra-Mediterranean (Portugal) and Mediterranean (Greece)] have evolved different survival and reproductive schedules. Whereas females were either short-lived [life expectancy at eclosion (e0) 48,58 days; Kenya, Hawaii and Guatemala] or long-lived (e0 72,76 days; Greece, Portugal and Brazil], males with one exception (Guatemala) were generally long-lived (e0 106,122 days). Although males universally outlived females in all populations, the longevity gender gap was highly variable (20,58 days). Lifetime fecundity rates were similar among populations. However, large differences were observed in their age-specific reproductive patterns. Short-lived populations mature at earlier ages and allocate more of their resources to reproduction early in life compared with long-lived ones. In all populations, females experienced a post-reproductive lifespan, with this segment being significantly longer in Kenyan flies. Therefore, it seems plausible that medfly populations, inhabiting ecologically diverse habitats, have evolved different life history strategies to cope with local environmental conditions. © 2009 The Linnean Society of London, Biological Journal of the Linnean Society, 2009, 97, 106,117. [source] | ||||||||||