Effects of Exposure Timing on cyp1a Expression, PAH Elimination, and Lipid Utilization in Lumpfish Embryos Exposed to Produced Water.

Intentional discharges of produced water from oil production platforms to the marine environment contain a complex mixture of toxicants, including polycyclic aromatic hydrocarbons (PAHs). Early life stages of fish are highly sensitive to petrogenic exposure, and short-term exposure during critical periods of embryonic development may have detrimental effects on larvae health and survival. However, why different periods are more sensitive to exposure than others are not fully understood. Three identical exposure experiments (48 h, approx. 30 µg/L tPAH, sum 42 PAHs) on lumpfish (Cyclopterus lumpus) embryos were conducted where only exposure timing was varied: 0-48 h post fertilization (hpf, starting before chorion hardening), 36-84 hpf (starting after chorion hardening), and 240-288 hpf (during organogenesis). Total PAH (tPAH) uptake at the end of exposure was 5× higher when exposed during fertilization than when exposed late (during organogenesis). The first evidence of cyp1a induction in lumpfish during embryogenesis was observed after 84 hpf. Early exposure affected lipid droplet coagulation, indicating altered lipid utilization during embryogenesis. Although no significant impacts of exposure were observed on hatching success, hatching was delayed when exposed at the latest time point. This study shows that chorion properties, lipid content, biotransformation potential, and timing of produced water exposure during lumpfish embryogenesis affected PAH uptake and elimination.

Many lifetime growth trajectories for a single mammal.

Despite their importance in shaping life history tactics and population dynamics, individual growth trajectories have only been rarely explored in the wild because their analysis requires multiple measurements of individuals throughout their lifetime and some knowledge of age, a key timer of body growth. The availability of long-term longitudinal studies of two wild boar populations subjected to contrasting environments (rich vs. poor) provided an opportunity to analyze individual growth trajectories. We quantified wild boar growth trajectories at both the population and the individual levels using standard growth models (i.e., Gompertz, logistic, and monomolecular models) that encompass the expected range of growth shapes in determinate growers. Wild boar is a rather altricial species, with a polygynous mating system and is strongly sexually dimorphic in size. According to current theories of life history evolution, we thus expect wild boar to display a sex-specific Gompertz type growth trajectory and lower sexual size dimorphism in the poorer environment. While wild boar displayed the expected Gompertz type trajectory in the rich site at the population level, we found some evidence for potential differences in growth shapes between populations and individuals. Asymptotic body mass, growth rate and timing of maximum growth rate differed as well, which indicates a high flexibility of growth in wild boar. We also found a cohort effect on asymptotic body mass, which suggests that environmental conditions early in life shape body mass at adulthood in this species. Our findings demonstrate that body growth trajectories in wild boar are highly diverse in relation to differences of environmental context, sex and year of birth. Whether the intermediate ranking of wild boar along the precocial-altricial continuum of development at birth may explain the ability of this species to exhibit this high diversity of growth patterns remains to be investigated.

Grow fast at no cost: no evidence for a mortality cost for fast early-life growth in a hunted wild boar population.

From current theories on life-history evolution, fast early-life growth to reach early reproduction in heavily hunted populations should be favored despite the possible occurrence of mortality costs later on. However, fast growth may also be associated with better individual quality and thereby lower mortality, obscuring a clear trade-off between early-life growth and survival. Moreover, fast early-life growth can be associated with sex-specific mortality costs related to resource acquisition and allocation throughout an individual's lifetime. In this study, we explore how individual growth early in life affects age-specific mortality of both sexes in a heavily hunted population. Using longitudinal data from an intensively hunted population of wild boar (Sus scrofa), and capture-mark-recapture-recovery models, we first estimated age-specific overall mortality and expressed it as a function of early-life growth rate. Overall mortality models showed that faster-growing males experienced lower mortality at all ages. Female overall mortality was not strongly related to early-life growth rate. We then split overall mortality into its two components (i.e., non-hunting mortality vs. hunting mortality) to explore the relationship between growth early in life and mortality from each cause. Faster-growing males experienced lower non-hunting mortality as subadults and lower hunting mortality marginal on age. Females of all age classes did not display a strong association between their early-life growth rate and either mortality type. Our study does not provide evidence for a clear trade-off between early-life growth and mortality.