Acid exposure in euryhaline environments: ion regulation and acid tolerance in larval and adult Artemia franciscana

Mortality, and whole-body levels of [Na], [Cl] and [K]were measured in adult and naupliar stages of Brine Shrimp, Artemia franciscana, after 24h exposure to a waters of a range of acid (H₂SO₄)concentrations (pH 8.3 to 4.5). Acid effects were tested in both dilute (20%) and full strength artificial seawater (ASW). All stages showed high sensitivity to acid stress whether tested in 20% or100% ASW. Nauplii were more sensitive than adults in either medium. Mortality in each case was correlated with dramatic changes in whole body [Na] and [Cll but animals in 20% ASW lost [Na] and [Cl] to the environment while animals in 100% ASW gained them from the environment. Clearly animals which ion-regulate in euryhaline media are more sensitive than expected to acid stress which may thus pose a serious threat to sensitive euryhaline habitats. This revised version was published online in August 2006 with corrections to the Cover Date.     

Population regulation and role of mesozooplankton in shaping marine pelagic food webs

Copepods constitute the majority of the mesozooplankton in the oceans.By eating and being eaten copepods have implications for the flow of matterand energy in the pelagic environment. I first consider populationregulation mechanisms in copepods by briefly reviewing estimates of growthand mortality rates and evidence of predation and resource limitation. Theeffects of variations in fecundity and mortality rates for the demography ofcopepod populations are then examined by a simple model, which demonstratesthat population growth rates are much more sensitive to variations inmortality than to variations in fecundity. This is consistent with theobserved tremendous variation in copepod fecundity rates, relatively low andconstant mortality rates and with morphological and behavioralcharacteristics of pelagic copepods (e.g., predator perception and escapecapability, vertical migration), which can all be considered adaptations topredator avoidance. The prey populations of copepods, mainly protozoa(ciliates) and phytoplankton, may be influenced by copepod predation tovarying degrees. The highly variable morphology and the population dynamics(e.g., bloom formation) of the most important phytoplankton prey populations(diatoms, dinoflagellates) suggest that predation plays a secondary role incontrolling their dynamics; availability of light and nutrients as well ascoagulation and sedimentation appear generally to be more important. Thelimited morphological variation of planktonic ciliates, the well developedpredator perception and escape capability of some species, and the oftenresource-unlimited in situ growth rates of ciliates, on the other hand,suggest that copepod predation is important for the dynamics of theirpopulations. I finally examine the implications of mesozooplankton activityfor plankton food webs, particularly their role in retarding vertical fluxesand, thus, the loss of material from the euphotic zone. This revised version was published online in July 2006 with corrections to the Cover Date.     

THE EVOLUTIONARY GENETICS OF MALE LIFE-HISTORY CHARACTERS IN DROSOPHILA MELANOGASTER

Alternative models of the maintenance of genetic variability, theories of life-history evolution, and theories of sexual selection and mate choice can be tested by measuring additive and nonadditive genetic variances of components of fitness. A quantitative genetic breeding design was used to produce estimates of genetic variances for male life-history traits in Drosophila melanogaster. Additive genetic covariances and correlations between traits were also estimated. Flies from a large, outbred, laboratory population were assayed for age-specific competitive mating ability, age-specific survivorship, body mass, and fertility. Variance-component analysis then allowed the decomposition of phenotypic variation into components associated with additive genetic, nonadditive genetic, and environmental variability. A comparison of dominance and additive components of genetic variation provides little support for an important role for balancing selection in maintaining genetic variance in this suite of traits. The results provide support for the mutation-accumulation theory, but not the antagonistic-pleiotropy theory of senescence. No evidence is found for the positive genetic correlations between mating success and offspring quality or quantity that are predicted by “good genes” models of sexual selection. Additive genetic coefficients of variation for life-history characters are larger than those for body weight. Finally, this set of male life-history characters exhibits a very low correspondence between estimates of genetic and phenotypic correlations.     

Density and age-specific mortality

Age-specific mortality rates decelerate at older ages in laboratory populations in the MedflyCeratitis capitata. This has been interpreted by Careyet al. (1992) to reflect a slowing of the aging process, but might also be explained by declining adult density. Here it is argued that the density explanation, as presented by Graves and Mueller (1993), is unpersuasive for several reasons: extrapolations fromDrosophila to Medflies are unjustified; the range of densities they studied is 2–120 times higher than that used in other studies; they ignore data on Medflies held in isolation, which rule out density effects; their own data suggest that initial cohort density has no effect on mortality rates at older ages, which is the relevant part of the life cycle; their experiment is too small to provide accurate estimates of mortality; new Medfly experiments executed at multiple densities show decelerating and then declining mortality rates at advanced ages for all densities. WhenDrosophila survivorship experiments are done on a sufficiently large scale they also show a deceleration of mortality at older ages that is not attributable to density effects. The deceleration of mortality rates is most likely a real facet of aging, and will have to be taken into consideration in any synthesis of the genetics and evolution of aging.     

Catarrhine juvenile mortality in captivity,under seminatural conditions,and in the wild

Juvenile mortality is an important problem in the development of captive populations. I compiled data from published literature on abortion, premature mortality, stillbirth, and death of unweaned young. Cumulative mortality incidences (CMI) during the first month in captive populations (CP) of Cercopithecoidea range between 13 and 51%, and CMI in the first year between 28 and 56%. Mortality rate during the first year ranges between <4 and 48% in free- ranging populations (FRP) and between 10 and 60% in wild populations (WP). Much of the juvenile mortality in CP appears to occur in the first month, whereas in FRP and WP mortality is more scattered throughout the juvenile period. High mortality rates occur in both CP and WP of nonhuman Hominoidea. Mortality rate during the first month in CP is between 12 and 36% for the Hylobatidae and between 18 and 31% for the Pongidae. If the entire juvenile period is considered, gorilla CP and WP have comparable CMI, while CMI is higher in WP than CP for chimpanzees. Most of the juvenile mortality in CP of chimpanzees occurs before the age of 1 year. Trauma, including infanticide and maternal inadequacy, seems to be a more important factor in infant mortality of Cercopithecoidea than infectious disease is. Relatively frequent reports of congenital, hereditary, and/or genetically determined malformations in the Cercopithecoidea may be related to the long use of animals in this group for laboratory purposes. Infectious disease is the most important cause of nonhuman hominoid juvenile mortality, followed by trauma and maternal disorders, particularly related aberrant maternal behavior. Cercopithecoid juvenile mortality risk factors most frequently mentioned in the literature are sex of the infant and rank of the mother: dominant females produce more female offspring, and juvenile males suffer higher mortality than females do. The female skewed sex ratio at birth in gorillas and chimpanzees could be explained by the local resource competition theory. Higher male mortality rates occur in nonhuman Hominoidea, except in two Hylobatesspp. and Pan paniscus,which have higher female mortality. Parity and rearing history of the mother are very important risk factors in nonhuman hominoid infant mortality.     

Absence of deleterious effects of inbreeding in rhesus macaques

The limited availability of rhesus macaques through importation and the need for large numbers of them for use in biomedical research in this country have led to large- scale efforts to breed them domestically in captive groups. Since gene flow into the groups is usually restricted, consanguineous inbreeding can lead to inbreeding depression, which is characterized by increases in mortality, declines in fertility, and reductions in traits associated with physiological efficiency. For this reason, it is desirable to determine the level of inbreeding at which inbreeding depression occurs in rhesus macaques. I compared fertility, mortality, and the rate of weight gain in inbred and noninbred rhesus monkeys in three captive groups. There is no evidence of inbreeding depression in rhesus macaques whose inbreeding coefficients are ≤ 0.125, a level at which inbreeding depression is known to occur in some species.     

Platyrrhine juvenile mortality in captivity and in the wild

I reviewed literature on juvenile mortality in the Platyrrhini in order to evaluate reproductive success in captive breeding. Juvenile mortality includes abortion, premature mortality, stillbirth and death of the unweaned young. The highest losses occur in the Callitrichidae (31% through 3 months of age; 86% through 6 months of age) and in Lagothrixspp. (around 50% through 1 month of age) among the Cebidae. High abortion rates occur in Saguinusand Aotus.High stillbirth incidences are reported for the Callitrichidae (Callithrixand Saguinus)and for the Cebidae (Saimiriand Aotus).Although most mortality occurs in the first week for most species, a considerable proportion of deaths occurs in the period from week 1 until weaning. Important causes of death are trauma and aberrant parental behavior. Prematurity plays an important role in perinatal death among the Callitrichidae. Dystocia is a major cause of stillbirth in Saimiri. Congenital malformations occur in Callithrix, Saguinus, Leontopithecus,and Saimiri.Infectious diseases play a secondary role in mortality, particularly during the first period of life. A higher mortality risk is present if the infant is male, if the litter size is different from two (Callitrichidae), if the mother is primiparous, captive born, or inexperienced, or if the group is small (Callitrichidae) or unstable (Cebidae).     

Effect of temperature,humidity and photoperiod on mortality of Mononychellus tanajoa (Acari: Tetranychidae) infected by Neozygites cf. floridana (Zygomycetes: Entomophthorales)

The effect of temperature, humidity and photoperiod on the development of Neozygites cf. floridana (Weiser and Muma) in the cassava green mite, Mononychellus tanajoa (Bondar) was studied in the laboratory. Dead infected mites began to appear 2.5 days after inoculation. At 33 and 28°C peak mortalities were higher and occurred earlier (after 2.5 days), than at 23 and 18°C. Mean LT₅₀ (time for half the infected mites to die) decreased with increasing temperature as follows: 3.9, 3.0, 2.9 and 2.5 days at 18, 23, 28 and 33°C, respectively. When placed under conditions of high relative humidity for a period of 24 h, the percentage of dead infected mites from which the fungus sporulated was highest at 28°C (51.4%) and lowest at 33°C (6.5%). The development of the fungus inside the mite was not significantly affected by ambient humidity or photoperiod. No significant interactions between tested factors were found.     

MEASURING SELECTION ON A POPULATION OF DAMSELFLIES WITH A MANIPULATED PHENOTYPE

The estimation of the relationship between phenotype and fitness in natural populations is constrained by the distribution of phenotypes available for selection to act on. Because selection is blind to the underlying genotype, a more variable phenotypic distribution created by using environmental effects can be used to enhance the power of a selection study. I measured selection on a population of adult damselflies (Enallagma boreale) whose phenotype had been modified by raising the larvae under various levels of food availability and density. Selection on body size (combination of skeletal and mass at emergence) and date of emergence was estimated in two consecutive episodes. The first episode was survival from emergence to sexual maturity and the second was reproductive success after attaining sexual maturity. Female survival to sexual maturity was lower, and therefore opportunity for selection greater, than males in both years. Opportunity for selection due to reproductive success was greater for males. The total opportunity for selection was greater for males one year and for females the other. Survival to sexual maturity was related to mass gain between emergence and sexual maturity. Females gained more mass and survived less well than males in both years but there was no linear relationship between size at emergence and survival for females in either year. However, females in the tails of the phenotype distribution were less likely to survive than those near the mean. In contrast, small males consistently gained more mass than large males and survived less well in one year. There was significant selection on timing of emergence in both years, but the direction of selection changed due to differences in weather; early emerging females were more successful one year and late emerging males and females the other. The number of clutches laid by females was independent of body size. Because the resources used to produce eggs are acquired after emergence and this was independent of size at emergence, female fitness did not increase with size. Small males may have had lower survival to sexual maturity but they had higher mating success than large males. Resources acquired prior to sexual maturity are essential for reproductive success and may in some species alter their success in inter- and intrasexual competition. Therefore, ignoring the mortality associated with resource acquisition will give an incomplete and potentially misleading picture of selection on the phenotype.     

The Influence of Topography on Tree Growth,Mortality, and Recruitment in a Tropical Montane Forest1

To determine if there were consistent differences in growth, mortality, and recruitment on slopes and ridge crests in tropical montane forests, which could explain the (frequent but not universal) low stature of trees in the ridgetop forests, we analyzed data from long‐term plots in Jamaica (1990–1994; sixteen 200‐m² plots, six on ridge crests and five each on north and south slopes). Mortality was higher on north slopes, while growth and recruitment rates were not significantly different among positions. Soil pH and effects of recent disturbance by Hurricane Gilbert were positively correlated with growth and recruitment, while slope angle and disturbance effects were the best predictors of mortality. The patterns we found in Jamaica, that growth and recruitment were not higher on ridge crests than slopes, are different than those found by Herwitz and Young in Australia where growth and turnover were greater on a ridge crest. Therefore, it is not possible at present to make simple generalizations about dynamics of ridge crest versus slope forests in the montane tropics.