Evolution of sexual size dimorphism in grouse and allies (Aves: Phasianidae) in relation to mating competition,fecundity demands and resource division

Sexual size dimorphism (SSD) is often assumed to be driven by three major selective processes: (1) sexual selection influencing male size and thus mating success, (2) fecundity selection acting on females and (3) inter‐sexual resource division favouring different size in males and females to reduce competition for resources. Sexual selection should be particularly strong in species that exhibit lek polygyny, since male mating success is highly skewed in such species. We investigated whether these three selective processes are related to SSD evolution in grouse and allies (Phasianidae). Male‐biased SSD increased with body size (Rensch’s rule) and lekking species exhibited more male‐biased SSD than nonlekking ones. Directional phylogenetic analyses indicated that lekking evolved before SSD, but conclusions were highly dependent on the body size traits and chosen model values. There was no relationship between SSD and male display agility, nor did resource division influence SSD. Although clutch mass increased with female body size it was not related to the degree of SSD. Taken together, the results are most consistent with the hypothesis that lekking behaviour led to the evolution of male‐biased SSD in Phasianidae.     

Variation in life-history characteristics among populations of North American wood turtles: a view from the north

Life-history traits such as age at maturity, body size and clutch size tend to vary across a species' distribution. The purpose of our study was to describe the demography of a newly discovered population of North American wood turtles Glyptemys insculpta at the species' northern range limit, and to compare our findings to those of other studies to test hypotheses about adaptive life-history variation. Turtles were hand-captured from May to October 2005 and 2006 along a 4.5 km stretch of river located in the Sudbury District, ON, Canada (46°N). Fifty-five captured individuals provided a population density estimate of 1.3 turtles/100 m of river. Juveniles comprised 35% of wood turtles captured, and growth ring counts (i.e. age estimates) indicated recruitment in each of the past 11 years. Among populations, we found a nonlinear pattern in body size variation with the largest turtles in the north, smallest turtles in the centre of the range, and intermediate-sized turtles in the south. This nonlinear pattern in body size was reflected in clutch size variation. Selective pressures to overcome years of low recruitment may have resulted in larger body sizes and hence large clutch sizes at northern latitudes while conspecifics at southern latitudes can achieve larger body sizes because they live in a more productive environment. Population density decreased with latitude, likely as a result of a gradient in habitat productivity.     

Seasonal variation in the reproductive strategy of the parasitic wasp Eulophus larvarum (Hymenoptera: Chalcidoidea: Eulophidae)

ABSTRACT. 1. Eulophus larvarum (L.) (Hymenoptera: Eulophidae) is a gregarious parasitoid of lepidopterous larvae feeding on broad-leaved trees. Normally there are two generations a year.
2. Sex ratio in the spring generation of larvae is female biased. The bias is probably due to local mate competition as progeny from one brood emerge from their pupae in close proximity to each other.
3. Sex ratio in the summer generation of larvae is near equality. Local mate competition is absent as individuals from the same brood become separated during the winter.
4. Variation in sex-ratio in the spring generation is consistent with a binomial model. Variation in sex ratio in the summer generation is much greater than expected from a binomial model and there is a large proportion of single-sex broods.
5. Two hypotheses are put forward to explain the summer generation pattern: virgin oviposition, and strong intersexual competition.
6. No differences in clutch size were found between the two generations.     

Evolution of avian clutch size along latitudinal gradients: do seasonality,nest predation or breeding season length matter?

Birds display a latitudinal gradient in clutch size with smaller clutches in the tropics and larger in the temperate region. Three factors have been proposed to affect this pattern: seasonality of resources (SR), nest predation and length of the breeding season (LBS). Here, we test the importance of these factors by modelling clutch size evolution within bird populations under different environmental settings. We use an individual‐based ecogenetic simulation model that combines principles from population ecology and life history theory. Results suggest that increasing SR from the tropics to the poles by itself or in combination with a decreasing predation rate and LBS can generate the latitudinal gradient in clutch size. Annual fecundity increases and annual adult survival rate decreases from the tropics to the poles. We further show that the annual number of breeding attempts that (together with clutch size) determines total annual egg production is an important trait to understand latitudinal patterns in these life history characteristics. Field experiments that manipulate environmental factors have to record effects not only on clutch size, but also on annual number of breeding attempts. We use our model to predict the outcome of such experiments under different environmental settings.     

Allen's rule revisited: quantitative genetics of extremity length in the common frog along a latitudinal gradient

Ecogeographical rules linking climate to morphology have gained renewed interest because of climate change. Yet few studies have evaluated to what extent geographical trends ascribed to these rules have a genetic, rather than environmentally determined, basis. This applies especially to Allen's rule, which states that the relative extremity length decreases with increasing latitude. We studied leg length in the common frog (Rana temporaria) along a 1500 km latitudinal gradient utilizing wild and common garden data. In the wild, the body size-corrected femur and tibia lengths did not conform to Allen's rule but peaked at mid-latitudes. However, the ratio of femur to tibia length increased in the north, and the common garden data revealed a genetic cline consistent with Allen's rule in some trait and treatment combinations. While selection may have shortened the leg length in the north, the genetic trend seems to be partially masked by environmental effects.     

桓仁滑蜥生殖行为及生殖策略的研究

桓仁滑蜥（Scincella huanrensis）系卵胎生,1年生殖1次,生殖季节为7月下旬到8月上旬。平均每只雌蜥产仔4．556（2～6）只。雌蜥的分娩在洞穴中进行,分娩时间可持续60-90min,仔蜥在产出时卵膜已破裂。雌性采取的是高投入的生殖策略,平均生殖投入率0．436（0．212～0．526）。相关性回归分析表明：窝仔数与雌蜥体重、体长和生殖投入呈正相关关系;生殖投入与雌蜥的体重和体长不相关;幼蜥的体长、体重与窝仔数呈负相关关系。     

Why get big in the cold? Size–fecundity relationships explain the temperature‐size rule in a pulmonate snail (Physa)

Most ectotherms follow a pattern of size plasticity known as the temperature‐size rule where individuals reared in cold environments are larger at maturation than those reared in warm environments. This pattern seems maladaptive because growth is slower in the cold so it takes longer to reach a large size. However, it may be adaptive if reaching a large size has a greater benefit in a cold than in a warm environment such as when size‐dependent mortality or size‐dependent fecundity depends on temperature. I present a theoretical model showing how a correlation between temperature and the size–fecundity relationship affects optimal size at maturation. I parameterize the model using data from a freshwater pulmonate snail from the genus Physa. Nine families were reared from hatching in one of three temperature regimes (daytime temperature of 22, 25 or 28 °C, night‐time temperature of 22 °C, under a 12L : 12D light cycle). Eight of the nine families followed the temperature‐size rule indicating genetic variation for this plasticity. As predicted, the size–fecundity relationship depended upon temperature; fecundity increases steeply with size in the coldest treatment, less steeply in the intermediate treatment, and shows no relationship with size in the warmest treatment. Thus, following the temperature‐size rule is adaptive for this species. Although rarely measured under multiple conditions, size–fecundity relationships seem to be sensitive to a number of environmental conditions in addition to temperature including local productivity, competition and predation. If this form of plasticity is as widespread as it appears to be, this model shows that such plasticity has the potential to greatly modify current life‐history theory.     

Selection on a eumelanic ornament is stronger in the tropics than in temperate zones in the worldwide‐distributed barn owl

Spatial variation in the pattern of natural selection can promote local adaptation and genetic differentiation between populations. Because heritable melanin‐based ornaments can signal resistance to environmentally mediated elevation in glucocorticoids, to oxidative stress and parasites, populations may vary in the mean degree of melanic coloration if selection on these phenotypic aspects varies geographically. Within a population of Swiss barn owls (Tyto alba), the size of eumelanic spots is positively associated with survival, immunity and resistance to stress, but it is yet unknown whether Tyto species that face stressful environments evolved towards a darker eumelanic plumage. Because selection regimes vary along environmental gradients, we examined whether melanin‐based traits vary clinally and are expressed to a larger extent in the tropics where parasites are more abundant than in temperate zones. To this end, we considered 39 barn owl species distributed worldwide. Barn owl species living in the tropics displayed larger eumelanic spots than those found in temperate zones. This was, however, verified in the northern hemisphere only. Parasites being particularly abundant in the tropics, they may promote the evolution of darker eumelanic ornaments.     

Is body size a good indicator of fecundity in the genus Thaumetopoea? A story told by two intrageneric Mediterranean forest defoliators

1. Body size correlates with several factors such as reproductive fitness, environmental changes, the quality and quantity of food during critical development stages, and the feeding season. For the Palearctic moths of the genus Thaumetopoea (Lepidoptera; Notodontidae), the larval development is crucial and differs between species according to their feeding season; larvae of the pine processionary moth Thaumetopoea pityocampa (Denis & Schiffermüller 1775) feed during winter while larvae of its congeneric cedar processionary moth Thaumetopoea bonjeani (Powell 1922) develop during summer in North Africa.
2. This discrepancy in lifecycles leads to different reproductive traits such as egg batch length, number of eggs per batch, eggs protection mechanisms and female body size.
3. According to Darwin's fecundity advantage hypothesis (1871), female body size should have a positive influence on reproductive fitness, since larger females supposedly have higher fecundity. The universal allometric scaling phenomenon rule proposed by Rensch (1950) predicts that the degree of sexual size dimorphism tends to decrease with the increase of female body size.
4. Here, two morphometrical parameters that is, body size and scale size, estimated from body measurements of individuals of both species, feeding on the same host Atlantic cedar Cedrus atlantica (Manetti & Carrière 1855) (Pinales; Pinaceae) in Algeria were proposed. The aim was to find out traits that might rule the competition for food and space, in particularly fecundity and body size.
5. Results of the present study highlight a female-biased sexual size dimorphism in both species. The positive correlation between female body size and fecundity shown in this study weakly supports Darwin's hypothesis. Finally, the intrageneric test performed leads to conclude that Rensch's rule does not hold in the considered species.

     

中国林蛙的生殖量特征及其地理变化

标本采自山西省境内的８个地点。结果表明１研究区域内性成熟雌蛙平均体长范围是３４．５－５２．３ｍｍ,高山森林带种群明显偏高;研究种群雌蛙的体长显著低于东北居群。２平均生殖量的范围是４２２．４－８４０．９枚,个体的最低,最高值分别为３８和１９７８枚,平均相对生殖量的范围是１０．７－１８．０,个体的最低,最高值各为１．３和３４．４。与东北居群相比,生殖量的变异幅度较高。３除高山森林带外,其余调查点的生殖