Blue Cod, Parapercis Colias, Maturity, Fecundity, Sex Change, and Potential Drivers of Sex Ratio in The Marlborough Sounds

<p>Blue cod, Parapercis colias (Pinguipedidae), are widely considered to be the most important recreational finfish species in the South Island. However, blue cod have been declining in abundance in the Marlborough Sounds for many years, and currently, sex ratios are highly male- biased. Blue cod are believed to be a socially structured hermaphroditic species whose populations are prone to local depletion. A potting survey in the Marlborough Sounds was carried out by NIWA in 2013, and along with environmental measurements, 3247 blue cod were measured, weighed, sexed, and stage of sexual maturity was classified macroscopically at sea. Gonads from a subsample of these fish were removed and preserved. In Chapter Two, the preserved gonads were processed histologically and a species-specific histological maturity key was developed. Histological and macroscopic maturity classifications and length-at-maturity estimates were compared. Additionally, estimates of spawning frequency and batch fecundity were made using histological and gravimetric methods. In Chapter Three, possible drivers of sex ratio were investigated using the survey data. Density, large male influence, and environmental factors were considered. In Chapter Four, the feasibility of using digital imaging software to age blue cod otoliths was investigated using the OtolithM application in ImagePro Premier. There was poor agreement between macroscopic and histological maturity classifications (20%, overall). Macroscopic methods overestimated the proportion of mature fish at length in the larger sample, which led to biased length-at-50% maturity (L₅₀) estimates. Macroscopic L₅₀ estimates differed markedly from histology estimates. Using histological data, male L₅₀ was 26 cm TL. Histology indicated that there was no length at which 100% of females were mature. Therefore, a three-parameter capped logistic model was used. Histologically, female L₅₀ was 23.6 cm TL, and the Cap was 0.78, indicating the proportion of mature females reached an asymptote at 0.78. Spawning frequency was 4.6 days, and mean relative batch fecundity was 6.5 hydrated oocytes per gram body weight (SD = 3.3). Hermaphroditism was confirmed for blue cod and was macroscopically identifiable. The analyses in Chapter Three indicated that density had some effect on sex ratio, and large males influenced local sex ratios. Finally, the imaging software could not accurately estimate age compared to an expert reader, and it produced highly variable age estimates. This research found that the macroscopic maturity classifications for blue cod were inaccurate, and revision of the macroscopic key is suggested. The biased estimates of L₅₀ from macroscopic data could lead to biased estimates of spawning stock biomass (SSB). Batch fecundity was markedly lower than the previously reported estimates. The finding of a macroscopically identifiable hermaphroditic stage suggested that ‘hermaphrodite’ should be added as a sex class in the macroscopic key. From the GLM in Chapter Three, in more dense populations, the proportion of males increased. This may have been from changes to male mating strategies, or density may influence the occurrence of primary and secondary males. Finally, areas with males > 45 cm TL had a higher proportion of females, suggesting that large males should be protected in order to help balance sex ratios.</p>

Blue Cod, Parapercis Colias, Maturity, Fecundity, Sex Change, and Potential Drivers of Sex Ratio in The Marlborough Sounds

<p>Blue cod, Parapercis colias (Pinguipedidae), are widely considered to be the most important recreational finfish species in the South Island. However, blue cod have been declining in abundance in the Marlborough Sounds for many years, and currently, sex ratios are highly male- biased. Blue cod are believed to be a socially structured hermaphroditic species whose populations are prone to local depletion. A potting survey in the Marlborough Sounds was carried out by NIWA in 2013, and along with environmental measurements, 3247 blue cod were measured, weighed, sexed, and stage of sexual maturity was classified macroscopically at sea. Gonads from a subsample of these fish were removed and preserved. In Chapter Two, the preserved gonads were processed histologically and a species-specific histological maturity key was developed. Histological and macroscopic maturity classifications and length-at-maturity estimates were compared. Additionally, estimates of spawning frequency and batch fecundity were made using histological and gravimetric methods. In Chapter Three, possible drivers of sex ratio were investigated using the survey data. Density, large male influence, and environmental factors were considered. In Chapter Four, the feasibility of using digital imaging software to age blue cod otoliths was investigated using the OtolithM application in ImagePro Premier. There was poor agreement between macroscopic and histological maturity classifications (20%, overall). Macroscopic methods overestimated the proportion of mature fish at length in the larger sample, which led to biased length-at-50% maturity (L₅₀) estimates. Macroscopic L₅₀ estimates differed markedly from histology estimates. Using histological data, male L₅₀ was 26 cm TL. Histology indicated that there was no length at which 100% of females were mature. Therefore, a three-parameter capped logistic model was used. Histologically, female L₅₀ was 23.6 cm TL, and the Cap was 0.78, indicating the proportion of mature females reached an asymptote at 0.78. Spawning frequency was 4.6 days, and mean relative batch fecundity was 6.5 hydrated oocytes per gram body weight (SD = 3.3). Hermaphroditism was confirmed for blue cod and was macroscopically identifiable. The analyses in Chapter Three indicated that density had some effect on sex ratio, and large males influenced local sex ratios. Finally, the imaging software could not accurately estimate age compared to an expert reader, and it produced highly variable age estimates. This research found that the macroscopic maturity classifications for blue cod were inaccurate, and revision of the macroscopic key is suggested. The biased estimates of L₅₀ from macroscopic data could lead to biased estimates of spawning stock biomass (SSB). Batch fecundity was markedly lower than the previously reported estimates. The finding of a macroscopically identifiable hermaphroditic stage suggested that ‘hermaphrodite’ should be added as a sex class in the macroscopic key. From the GLM in Chapter Three, in more dense populations, the proportion of males increased. This may have been from changes to male mating strategies, or density may influence the occurrence of primary and secondary males. Finally, areas with males > 45 cm TL had a higher proportion of females, suggesting that large males should be protected in order to help balance sex ratios.</p>

Inferring Preferred Mating Strategies Through Body Fat and Sex-Typical Body Features

Identifying reproductive opportunities and intrasexual rivals has necessitated the evolution of sensitivity to features diagnostic of mate value. In determining the presence of good genes through physical features, individuals may additionally infer targets’ short- and long-term mating motives. This study tested how individuals perceive men and women’s mating intentions through physical features conducive to reproductive goals. Participants evaluated preferred mating strategies of male and female targets varying in size of sex-typical features (i.e., muscles or breasts) and adiposity. Greater adiposity connoted long-term mating interest. Large muscles and breasts connoted short-term mating interests. We frame results from an affordance management framework with respect to inferences regarding parental investment and intrasexual competition.

Deducing how tropical rhyssines (Hymenoptera, Ichneumonidae) mate from body measurements

The biology of many Darwin wasp (Hymenoptera: Ichneumonidae) species is poorly known. Existing museum specimens can potentially be used to get information on e.g. how species live, what they eat, and what their life cycle is. One example of this is a 1991 study by Eggleton in which he measured some rhyssine (Ichneumonidae: Rhyssinae) species, and used the results to deduce how the species likely mate. We extend this work by measuring five tropical species. We found no evidence that the males of our species scramble for females before the females emerge, which matches what was hypothesised by Eggleton. Further measurements of more species would provide information on how other species mate, and field observations of mating rhyssines would help confirm that Eggleton’s method for deducing rhyssine mating strategies gives true results.

Sex differences in the reward value of familiar mates in prairie voles

The rewarding properties of social interactions facilitate relationship formation and maintenance. Prairie voles are one of the few laboratory species that form selective relationships, manifested as "partner preferences" for familiar partners versus strangers. While both sexes exhibit strong partner preferences, this similarity in outward behavior likely results from sex-specific neurobiological mechanisms. We recently used operant conditioning to demonstrate that females work harder for access to a familiar versus unfamiliar conspecific of either sex, while males worked equally hard for access to any female, indicating a key sex difference in social motivation. As tests were performed with one social target at a time, males might have experienced a ceiling effect, and familiar females might be more relatively rewarding in a choice scenario. Here we performed a social choice operant task in which voles could repeatedly lever-press to gain temporary access to either the chamber containing their mate or one containing a novel opposite-sex vole. Females worked hardest to access their mate, while males pressed at similar rates for either female. Individual male behavior was heterogeneous, congruent with multiple mating strategies in the wild. Voles exhibited preferences for favorable over unfavorable environments in a non-social operant task, indicating that lack of social preference does not reflect lack of discrimination between chambers. Oxytocin receptor genotype at the intronic SNP NT213739 replicated a prior association with stranger-directed aggression within the test. These findings suggest that convergent preference behavior in male and female voles results from sex-divergent pathways, particularly in the realm of social motivation.

Sex Differences in Attitudes Toward Casual Sex: Using STI Contraction Likelihoods to Assess Evolved Mating Strategies

Previous work shows that males are more likely to pursue casual sex if given the opportunity, compared to females, on average. One component of this strategy is risk-taking, and males have been shown to take more risks than females in a variety of contexts. Here, we investigate the extent to which sex differences exist considering casual sexual encounters involving sexually transmitted infections (STIs) using a hypothetical sexual scenario which attempts to circumvent several factors that may contribute to a female’s hesitancy to engage in casual sex encounters. Two hundred and forty-six college students rated their willingness to engage in a satisfying casual sexual encounter with someone judged to be personable as a function of sex, varying STI contraction likelihoods, several STI types, and two levels of hypothetical partner attractiveness. We also assess how individual levels of sociosexuality (as measured by the SOI-R) impact findings. Our findings show that males report higher likelihoods of sexual engagement compared to females in general. This trend continued for lower likelihoods of STI contraction in all four STI types (Cold, Chlamydia, Herpes, HIV), with larger effects shown in the high attractiveness partner condition. For higher STI contraction likelihoods and more severe STI types, along with lower partner attractiveness levels, sex differences shrank. Factoring in participant SOI-R scores attenuated the effects somewhat, although it failed to alter findings substantially with predicted sex differences continuing to exist. These results offer further insight into evolved sex differences in human mating systems and provide an additional framework to test sexual risk-taking among males and females.

Sexual morph specialisation in a trioecious nematode balances opposing selective forces.

The coexistence of different mating strategies, whereby a species can reproduce both by selfing and outcrossing, is an evolutionary enigma that has long intrigued biologists (Darwin, 1877). Theory predicts only two stable mating states : outcrossing with strong inbreeding depression or selfing with weak inbreeding depression. As these two mating strategies are subject to opposing selective forces, mixed breeding systems are thought to be a rare transitory state, yet they have been found to persist even after multiple speciation events. We hypothesise that if each mating strategy plays a distinctive role during the species life history, opposing selective pressures could be balanced, permitting the stable co-existence of selfing and outcrossing sexual morphs. In this scenario, we would expect each sexual morph to be specialised in their respective roles. Here we show, using a combination of behavioural, physiological and gene expression studies, that the selfing (hermaphrodite) and outcrossing (female) sexual morphs of the trioecious nematode Auanema freiburgensis have distinct adaptations optimised for their different roles during the life cycle. A. freiburgensis hermaphrodites are produced under stressful conditions, are specialised for dispersal to new habitat patches and exhibit metabolic and intestinal changes that enable them to meet the energetic cost of dispersal and reproduction. In contrast, A. freiburgensis females are produced in favourable conditions, facilitate rapid population growth and compensate for the lack of reproductive assurance by reallocating resources from intestinal development to robust mate-finding behaviour. The specialisation of each mating system for their role in the life cycle could balance opposing selective forces allowing the stable maintenance of both outcrossing and selfing mating systems in A. freiburgensis.