Search results for "behavior"

Evolutionary population dynamics

2005

The interface between the evolution of life history traits and population dynamics in temporally and spatially variable environments is the topic of this chapter. Thus, the frame for the life history processes is set by spatial and temporal fluctuations in population density. Here, we will focus primarily on modes of reproduction and we are especially interested in whether alternative reproductive strategies can co-exist in a population. We show that spatially structured populations may allow co-existence of various life history strategies that do not easily co-exist in a nonstructured environment. Also, intrinsic and external temporal fluctuations in the environment tend to enhance polymor…

Synchronicity in population systems: cause and consequence mixed

1999

Harvesting‐induced population fluctuations?

2003

It has recently been shown that damped endogenous dynamics is a common feature in Finnish grouse species; In this paper, we demonstrate that time-variant harvesting may turn damped dynamics to quasi-periodic fluctuations. Exploited populations, e.g. grouse, may therefore fluctuate more than expected if we do not manage to keep the harvest fraction constant over time. However, the harvest fraction of Finnish grouse varies with the phase of the cycle. Such a harvesting strategy could potentially change the periodicity of the fluctuations, as can a threshold harvest strategy where a constant fraction is harvested above a density threshold. The two non-linear harvesting strategies investigated …

PERMANENT GENETIC RESOURCES: Polymorphic microsatellite loci and interspecific cross-amplification in the parasitoid wasps Megastigmus stigmatizans a…

2008

We isolated and characterized 19 polymorphic microsatellite loci in the congeneric parasitoid wasps Megastigmus stigmatizans and Megastigmus dorsalis associated with cynipid oak galls. Loci isolated from species-specific libraries showed extensive cross-amplification, resulting in a total of 15 polymorphic loci for M. stigmatizans and 13 for M. dorsalis.

2020

Abstract To understand how variation in warning displays evolves and is maintained, we need to understand not only how perceivers of these traits select color and toxicity but also the sources of the genetic and phenotypic variation exposed to selection by them. We studied these aspects in the wood tiger moth Arctia plantaginis, which has two locally co-occurring male color morphs in Europe: yellow and white. When threatened, both morphs produce defensive secretions from their abdomen and from thoracic glands. Abdominal fluid has shown to be more important against invertebrate predators than avian predators, and the defensive secretion of the yellow morph is more effective against ants. Her…

Blood parasites mediate morph-specific maintenance costs in a colour polymorphic wild bird

2011

Parasites can mediate profound negative effects on host fitness. Colour polymorphism has been suggested to covary genetically with intrinsic physiological properties. Tawny owl colour polymorphism is highly heritable with two main morphs, grey and brown. We show that experimental medication acts to reduce blood parasites and that medicated grey females maintain body mass during breeding, whereas medicated brown females decline in body mass similar to control females of both morphs. We find no effect of medication on general immunoglobulin levels, antigen-specific humoral response or H/L ratio. In the descriptive data, both morphs have similar blood parasite infection rates, but blood parasi…

Do colour morphs of wall lizards express different personalities?

2021

Abstract Colour morphs sometimes have different behavioural strategies which may be maintained by frequency or density dependence mechanisms. We investigated temporal changes in behavioural reaction to a novel environment among colour morphs (yellow, orange, white) of the European wall lizard (Podarcis muralis). Adult males were given two 15 min experimental trials, and their locomotion was highly consistent between the two trials. Boldness, freezing and escape behaviour were less repeatable. Colour morphs differed in their locomotion and freezing behaviour. Boldness was similar among the morphs, whereas escape behaviour was lowest in yellow morph. Consequently, yellow morph males tended to…

‘Communication breakdown’: the evolution of signal unreliability and deception

2014

For a signalling system to be stable, signals must confer net fitness benefits to senders and receivers, which means that some aspect of their design must correlate with a quality that receivers benefit from knowing about. However, examples abound where this correlation is complicated by phenomena commonly referred to as deception and/or signal unreliability. We argue here that unreliability and deception are notions marred with conceptual ambiguities, often used as equivalent or as catch-all terms for qualitatively different processes. Signal unreliability refers to a pattern of design–information dissociation that can arise through different processes, some deceptive and some not, with di…

The Unique Characteristics of the Horses for Humans Learning Purposes in Equine Assisted Learning Practice

2019

This article aims to encourage scientific discussion about one of the aspects of equine-assisted learning practice, the unique characteristics of the horse owing to how it is used in intervention programmes for human learning purposes. Equine-assisted learning is an innovative learning approach where human learning and development takes place through guided interactions between humans and horses. Although scientific interest towards human-horse interactions is becoming increasingly popular, evidence-based research has examined the relationship between humans and horses, and how such bonds may contribute to human learning and development is limited and lacks empirical support. This report pr…

Fight or flight trade-offs and the defensive behaviour of the mountain katydid, Acripeza reticulata

2020

The defensive repertoires of prey are shaped by diverse ecological and evolutionary demands. This can generate trade-offs between the components of defences, as in the classic ‘fight or flight’ dichotomy, or dedicated investment in a singular end, allowing individuals in better condition to mount a more effective defence all round. Further, sexual dimorphism may drive sex differences in such responses, although our understanding of the interaction between sexual selection and defensive behaviour is in its infancy. Deimatic, or ‘startle’, defences typically combine multiple protective strategies, such as camouflage and aposematism, with a rapid transition between them, and thus offer unique …