The downfall of mating: the effect of mate-carrying and flight muscle ratio on the escape ability of a pierid butterfly

In many species, the ability to evade predators is known to be periodically impaired by increased weight loads due to feeding and reproduction. Not only may extra weight reduce escape speed, but feeding and mating can also make the prey more noticeable to visually hunting predators. A number of butterfly species mate for hours, and if a mating couple is disturbed, one of the butterflies is responsible for flying, whereas its partner remains still. This study investigated the ability of male Pieris napi butterflies to fly while mating, with the prediction that mate carrying impairs flight ability compared to single flying males and that males with relatively high flight muscle ratios (FMR; male thorax mass/male + female body mass) will have better flight performance in copula. Our results clearly show that whereas single males always take off at steep angles and fly upwards, couples invariably have a negative take-off angle and rarely gain height. Moreover, landing height of the couples is positively associated with higher FMR. Hence, male flight ability when in copula is positively associated with a high relative thorax mass. Butterfly pairs may thus be at greater risk of predation as a consequence of their impaired flight ability, especially couples with critically low FMRs (<16%).     

The rarity of twins: a result of an evolutionary battle between mothers and daughters—or do they agree?

The aim of this study was to test the hypothesis that parent–offspring conflict over parental investment might have led to the rarity of dizygotic twins in humans. We explored the theoretical prediction that twins maximize their inclusive fitness by the death of a co-twin, while mothers of twins maximize fitness by raising both twins to independence. We used life history data (1700–1900) from two parishes in Central Norway to compare differences in inclusive fitness (measured as number of children reared to the age of 16 years, using Hamilton's rule) between twins and mothers of twins. Our results show that twins maximize their inclusive fitness by the death of a co-twin, while mothers of twins raise more children by rearing both twins to adulthood. However, because twins growing up as singletons may produce higher or at least equal number of offspring than the sum of the two twins growing up together, mothers might gain more grandchildren by allowing twins to grow up as singletons. To conclude, both selfish twins and their mothers might benefit by the death of a co-twin, indicating that there is no parent–offspring conflict responsible for the rareness of twins in these human populations. Finally, we discuss the results in the light of “The Insurance Egg Hypothesis” and “The Natural Selection Hypothesis”.     

Cannibalize or care? The role of perceived paternity in the sand goby, <Emphasis Type="Italic">Pomatoschistus minutus</Emphasis>

Parental care is a costly part of reproduction. Hence, natural selection should favor males which avoid caring for unrelated young. However, the decision to abandon or reduce care requires cues which are evaluated to give information on potential reproductive value of the offspring. The prediction that male sand gobies, Pomatoschistus minutus, care for foreign eggs as long as they were spawned in their own nest and at least some of such cues are fulfilled was tested. Egg-guarding males that had recently taken part in a spawning event were given a clutch of eggs that was sired either by themselves or another male, in either their own or another male’s aquarium. Males that had not taken part in a spawning event were used as controls and were given eggs sired by another male. We measured the amount of filial cannibalism and nest building. Control group males did not care for eggs and ate them all before rebuilding the nest. In the other treatments, there were no significant effects of paternity, though males moved to another male’s aquarium increased their clutch area threshold and completely consumed larger clutches than males that were not moved. There was no intermediate response in any treatment in the form of increased partial filial cannibalism or less well-constructed nests. Our results suggest that egg-guarding males cannot distinguish between eggs sired by themselves and those sired by other males but are able to react to cues indicating paternity state. Males do not adopt eggs to attract females in P. minutus.     

Perspectives of farmers and tourists on agricultural abandonment in east Lesvos,Greece

Regional Environmental Change - Multi-stakeholder perceptions of landscape changes are increasingly recognized as essential inputs to discussions on future landscape developments, particularly when...     

Escape take-off strategies in birds: the significance of protective cover

Avian escape strategy is highly dependent on the ability to fly, and the success rate of raptor attacks is reduced if the prey gets fully airborne. Therefore, when escaping from predator attacks, the initial take-off is crucial and a rapid take-off, high velocity, and high angle of ascent maximize the chance of survival. However, due to the laws of gravity, birds face a trade-off between maximizing its linear acceleration and maximizing its rate of climb when taking off. The optimal policy between velocity and angle of ascent when a bird escapes from an attacking predator might depend on the detailed nature of the predator’s attack, the proximity to cover, and the presence of conspecifics. Many small birds rely on a quick dash to protective cover. In this study, we examine how the availability of protective cover affects take-off strategy in birds. Male great tits (Parus major) were subjected to a surprise attack by a model predator either in the presence or absence of protective cover. When attacked by the predator, great tits took off and perched in the cover when it was available. Birds subjected to the predator attack in the absence of cover took off in 10° higher angle of ascent and flew faster in the start of the take-off, compared to birds that took off in the presence of cover. Thus, this study for the first time shows that a bird do trade off speed with angle of ascent in an adaptive way, depending on the presence of protective cover.     

Uncertainties in Predictions of Surface Water Acidity using the MAGIC Model

In this study, we have used the MAGIC model together with data from the Birkenes catchment in Norway, at which 27 years of data (1974–2000) are available. We calibrated the MAGIC model to the five year observed average chemistry around 1990, and then used the data from the five year period around 1980 to refine the calibration. From 1990, forecasts were run for the different sets of inputs and parameters, and the sets of inputs and parameters were further refined using observations for the period 1996–2000. Through an automatic calibration routine, the model was calibrated a large number of times with different sets of input data to account for the uncertainties in the observed data using a Monte Carlo set-up. The results show that the uncertainty in the model predictions decreases as more observed data from different points in time are used in the model calibration. The results also show that when usingthe time series data in calibration, the distribution of the forecastchanged. The distribution of the predicted Acid Neutralisation Capacity (ANC) in the future is lower for the more refined model calibration. The 10 and 90 percentiles of predicted ANC in 2010 are –3 to 21 μeq L^-1 when only a five-year average is used for calibration, but are –7 to 9 μeq L^-1 when data from the three different time periods are used.     

Corrigendum

Distribution of 118 species of Amphipoda, Mysidacea and Decapoda, sampled in 1984 and 1985 with an epibenthic sledge along a transect from the Skagerrak to the inner Gullmarfjord (Sweden), is described. Amphipods were richest in species in the Skagerrak, while most mysid species were taken at the sill. Decapods did not display any clear pattern. Twinspan, a multivariate data analysis program, divided the samples into four groups: (I) deep-fjord samples; (II) sill, shallow-fjord and deep-basin samples; (III) sill samples; (IV) Skagerrak samples. Characteristic species of the groups were identified with a pseudoF-test. Detrended Correspondence Analysis indicated seasonal faunal changes at 42 and 72 m depths. At both depths a shift in numerical dominance from amphipods to mysids was found in winter. The most pronounced changes seemed to occur at 42 m. Changes in composition and abundance of species during a renewal of the bottom water indicated that mysids were influenced by presumed near-bottom currents, while amphipods and decapods were not. Comparison of the present amphipod fauna with the fauna in 1933–37 revealed significant differences. The fauna in the deep basin was impoverished and the Lilljeborgidae, earlier represented by three species, had disappeared since the 1930s. The changes are most likely caused by eutrophication of the fjord.     

The costs of secondary sexual characters in the lekking great snipe (Gallinago media)

Summary Recent studies of the lekking great snipe (Gallinago media) have shown that male mating success increases with display rate and the amount of white on the tail. An obvious question then arises: what is setting the limits to male display rate and to the evolution of even whiter tails? In this study the costs of these two traits are considered. In the case of the white on the tail, almost no predation was observed during the display period. However, predation on the winter grounds and/or during migration cannot be ruled out. Males differed in the amount of white on the tail between years. It is suggested that increasing the amount of white is costly, though the reason for this is still unknown. In the case of display rate, it is shown that predation cannot be a considerable cost, again because of the near absence of predation on the leks. Instead, it is shown that male displays are energetically costly. The daily energy expenditure of displaying males was estimated to be on average 4 times the basal metabolic rate, which is close to the supposed maximum sustainable work load for birds. Furthermore, males lost on average 1.8 g per h (1.7% of the body mass) which is about 7.2 g (6.8%) during a night of display activity. Males do gain some weight during the day when no displays are performed but loose on average 9 g during an 11-day period in the early part of the breeding season. These results indicate that high energetic demands set the limits to male display performance and that males do not have to trade off the benefit of attracting females by their displays against a cost of attracting predators. Offprint requests to: J. Höglund     

Assessing Secchi and photic zone depth in the Baltic Sea from satellite data

Long-term trends in the Secchi depth of the Baltic Sea have been interpreted in terms of eutrophication. The spectral attenuation coefficient Kd (490) can be estimated from remote sensing data. Given the empirical and theoretical relationships between diffuse attenuation and Secchi depth, it is therefore possible to estimate the trophic state from remote sensing data. This paper considers relationships among remotely sensed and in-water measured K (490), and Secchi depth data obtained during dedicated sea-truthing campaigns in the eastern Baltic Proper in 1999 (4) and in the western Baltic Proper/Himmerfj?rden area during 2001 and 2002. In-water measurements are used to establish the relationship between the PAR and the spectral attenuation coefficient in the Baltic Sea via regression analysis. The analysis showed that in the area of investigation Kd(490) is about 1.48 times higher than Kd (PAR). This relationship is then used to define the link between the photic zone depth and the remote sensing optical depth, Kd (490)-1. The results show that the depth of the euphotic zone is about 6.8 times Kd (490)-1. The regression analysis between Kd (PAR) and Secchi depth confirmed previous work that Kd (PAR) is about 1.7 of the inverse Secchi depth. Furthermore, an in-water algorithm between Secchi depth and Kd (490) is used to simulate a Secchi depth map of the Baltic Sea from SeaWiFS Kd(490) data. This map is verified against sea-truthing data. Kd (490) data derived from satellite is compared to in situ Kd (490), and the sources of error are discussed.