Carin Magnhagen

LATITUDINAL VARIATION IN LIFE‐HISTORY TRAITS IN EURASIAN PERCH

Few studies have examined multiple life-history traits across a latitudinal gradient to test whether variation in growth rate and mortality schedules induces trends predicted by life-history theory. We collected data for the following life-history traits for 75 Eurasian perch (Perca fluviatilis) populations: growth coefficient (K) and asymptotic body length (L∞) from the von Bertalanffy growth model, size at ages one and two years, specific juvenile growth rate, instantaneous adult and juvenile mortality rates, life span, age and length at maturity, and reproductive life span and investment. All life-history traits except L∞ were significantly correlated with latitude. In general, growth rates, mortality rates, and reproductive investment decreased with latitude, whereas age at maturity, size at maturity, and life span increased with latitude. Populations could be grouped into two categories based on variation in L∞: stunted (small sized) vs. piscivorous (large sized). Four trait–latitude relationships di...

Effects of sex ratio on intra- and inter-sexual behaviour in sand gobies

Reproductive behaviour and reproductive success in a marine fish, the sand goby, Pomatoschistus minutus, were affected by changes in the sex ratio. When the sex ratio was male biased (six males: three females), aggressive male-male interactions were more frequent per individual than in a female-biased situation (three males: six females). Accordingly, in the female-biased treatment females interacted more with each other than in the male-biased treatment. There was no difference between treatments in male interactions towards females, nor in female interactions towards males. Controls, with even sex ratios at two different densities (three or six of each sex), did not differ from each other in intra- or inter-sexual interactions. This shows that the differences in intra-sexual behaviour, found in males as well as females, were caused by the sex ratio and not by density. In the male-biased treatment and in the unbiased controls, nest-building males were larger than non-building males, whereas in the female-biased treatment there was no difference in size between builders and non-builders. Thus, our experiments show that a change in sex ratio changes competition for mates, and that individuals adjust their reproductive behaviour to the current sex ratio.

Express your personality or go along with the group: what determines the behaviour of shoaling perch?

Behavioural syndromes, defined as correlated behaviours in different contexts, have been studied across species and taxa including humans as part of a personality concept. While most studies have focused on solitary individuals, less is known on how shoaling fish compromise between own personality and group behaviour. Risk-taking behaviour in 1-year-old perch (Perca fluviatilis) was observed to compare individual behaviour when in a group and when alone. An experimental design gave the fish the choice between foraging in an open area in the presence of a piscivore and hiding in the vegetation. We quantified the variation accountable by the effect of individuals being in a group, individuals alone and repeated measurements, using hierarchical mixed effects models. Within-group variances were low, but when individuals were later tested alone, individual differences explained most of the variation. Still, the individual best linear unbiased predictors (BLUPs) of time spent in the open area, extracted from the random effects of the mixed effects model, were positively correlated with the corresponding BLUPs when alone. The results indicate that individual behavioural traits are to some degree expressed also within groups. Most fish showed a shyer behaviour when alone, but bolder individuals changed less between treatments than did shyer ones, suggesting a more influential role of bold fish in the group.

Is boldness affected by group composition in young-of-the-year perch (Perca fluviatilis)?

In young-of-the-year perch (Perca fluviatilis), individuals within groups differed in the degree of boldness, estimated by habitat utilisation and feeding activity in visual contact with a potential predator. We looked at changes in individual behaviour in connection with change of group composition. During the first period, perch were randomly assigned to groups, and time spent in open habitat versus in vegetation and number of prey attacks were registered. The perch were then categorised into ‘personality types’ (shy, bold, intermediate) according to their behaviour. During the second period, fish were observed when sorted into new groups, each containing only one personality type. Shy individuals showed the largest changes in behaviour, and increased both the time spent in the open and the number of prey attacks when placed into the new groups. Feeding activity in shy fish during the second period was affected by group composition during the first period. After regrouping, bold individuals decreased their time in the open, whereas intermediate individuals did not change behaviour. Time in the open habitat was, to some extent, influenced by the behaviour of the other members of the group, but number of prey attacks was not. The behaviour of fish of the different personality types we have defined in this study seemed to be based on innate traits, but also modified by the influence of other group members and by habituation to the environment.

Parental behaviour in relation to the occurrence of sneaking in the common goby

To investigate whether male common gobies, Pomatoschistus microps (Pisces, Gobiidae), treat their offspring differently depending on confidence of paternity, we conducted an experiment in which randomly chosen males either spawned alone with a female, or with a sneaking male present. Males did not treat their brood differently whether they had experienced sneaking or not. Our estimates of parental care, nest defence against potential egg predators and fanning rate were the same for the two treatments. Furthermore, there was no difference in filial cannibalism (eating their own progeny) between males that had been sneaked upon and males that had not. However, nest-guarding males that ate some of their brood had a smaller original brood area than other males. This suggests either an increase in paternal expenditure with increased brood size or a threshold value (absolute brood size or proportion of nest space covered) above which males do not cannibalize eggs. Copyright 1998 The Association for the Study of Animal Behaviour.

Social influence on the correlation between behaviours in young-of-the-year perch

The connection between risk-taking behaviour and exploratory behaviour in young-of-the-year perch (Perca fluviatilis) was studied in aquarium experiments to see whether individual behaviour patterns could be identified in this species and also to investigate how individual behaviour is influenced by their social environment. Risk-taking was defined as the time spent foraging in an open area vs hiding in the vegetation in the presence of a piscivore. Explorative behaviour was measured as latency to enter a passage leading to an unknown area. Groups of four fish were used for the observations, and both behaviours measured were positively correlated with the mean scores of these behaviours in the other group members. Risk-taking and explorative behaviours were correlated only when data was adjusted for the behaviour of the other group members. Individuals that spent more time in the open than their companions also tended to be faster than the others to enter the passage to the unknown area and vice versa. The results indicate that there are consistent individual differences in boldness in perch, but also that behaviour could be modified according to the behaviour of group members.

Brood size and offspring age affect risk-taking and aggression in nest-guarding common gobies

The importance of brood size, offspring age, and male size for parental care behaviour was studied in the common goby, Pomatoschistus microps. In field observations, the aggression of nest guarding males was measured as attacks towards a finger when disturbing the nest. Attacking males had larger and more developed clutches compared to non-attacking males, but did not differ in body size. In another set of observations nest guarding males were exposed to a predator (eelpout, Zoarces viviparus) and subsequently chased away from their nests. Time away from the nest decreased significantly with egg developmental stage, i.e. with the time the male had spent guarding a particular brood. However, no correlations with male body length or numbers of eggs in the nest were found. We conclude that male common gobies evaluate future reproductive success by using brood age and brood size as cues for making decisions about risk-taking and aggressive behaviour during parental care.

Risk-taking behaviour in foraging young-of-the-year perch varies with population size structure

I investigated if risk-taking behaviour of young-of-the-year (YOY) perch Perca fluviatilis was connected with population-specific predation patterns in four lakes in northern Sweden. The lakes differ in perch size distribution, according to earlier fishing surveys. Thus, the most intense predation pressure by cannibals is assumed to occur at different prey-size windows in the four lakes. In an aquarium study, I observed groups of perch, and registered time spent foraging in an open habitat and number of prey attacks in the presence of a predator. Perch from Ängersjön, with the highest proportion of large fish in the population, spent more time in the open area than those from Fisksjön that has a dense population of mainly small perch. The Ängersjön perch also made more prey attacks than did perch from Fisksjön and Bjännsjön. Relative differences in predation risk in the four lakes were estimated as cannibalistic attack rates, on a range of sizes of YOY perch, calculated from population size distributions. Principal component analysis on predation risk patterns resulted in two components, of which PC1 explained 79.1% of the variation. High scores of PC1 indicated low cannibalistic attack rates on smaller perch (10–20 mm) and high rates on larger fish (≥30 mm), while low scores indicated the opposite. The level of risk-taking behaviour in the aquarium study positively correlated with lake-specific PC1 scores. The perch with the most cautious behaviour in the aquaria originated from the population with the highest predation pressure on early stages. The boldest perch came from the lake with low predation on the smallest, but with higher predation on larger YOY perch. Thus, the influence of predation risk on behaviour patterns in perch may depend on the timing of the highest exposure to predators.

Boldness by habituation and social interactions: a model

Most studies of animal personality attribute personality to genetic traits. But a recent study by Magnhagen and Staffan (Behav Ecol Sociobiol 57:295–303, 2005) on young perch in small groups showed that boldness, a central personality trait, is also shaped by social interactions and by previous experience. The authors measured boldness by recording the duration that an individual spent near a predator and the speed with which it fed there. They found that duration near the predator increased over time and was higher the higher the average boldness of other group members. In addition, the feeding rate of shy individuals was reduced if other members of the same group were bold. The authors supposed that these behavioral dynamics were caused by genetic differences, social interactions, and habituation to the predator. However, they did not quantify exactly how this could happen. In the present study, we therefore use an agent-based model to investigate whether these three factors may explain the empirical findings. We choose an agent-based model because this type of model is especially suited to study the relation between behavior at an individual level and behavioral dynamics at a group level. In our model, individuals were either hiding in vegetation or feeding near a predator, whereby their behavior was affected by habituation and by two social mechanisms: social facilitation to approach the predator and competition over food. We show that even if we start the model with identical individuals, these three mechanisms were sufficient to reproduce the behavioral dynamics of the empirical study, including the consistent differences among individuals. Moreover, if we start the model with individuals that already differ in boldness, the behavioral dynamics produced remained the same. Our results indicate the importance of previous experience and social interactions when studying animal personality empirically.

Behaviour, physiology and carotenoid pigmentation in Arctic charr Salvelinus alpinus

The behaviour during an exploration task and the response to a confinement stress of Arctic charr Salvelinus alpinus were evaluated. Behaviour of individuals during 90 min of exploration was classified into high and low activity. High-activity individuals had higher plasma cortisol levels following stress compared to low-activity individuals. This indicates that high- and low-activity individuals correspond to reactive and proactive stress-coping styles. Further, a pigmentation analysis showed that high-activity individuals had a higher number of carotenoid spots cm⁻² than low-activity individuals. Thus, carotenoid pigmentation, as melanin pigmentation in other salmonids, could be linked to stress-coping style in S. alpinus.