Search results for "Systematics"

Exploring phylogeography and species limits in the Altai vole (Rodentia: Cricetidae)

2013

Natural hybridization between species is not a rare event. In arvicoline rodents, hybridization is known to occur in the wild and/or in captivity. In the Microtus arvalis group, cytogenetic studies revealed that there were two distinct chromosomal forms (2n = 46 but a different fundamental number of autosomes). These forms have been attributed to two cryptic species: the common (arvalis) and Altai (obscurus) voles. Recently, individuals with intermediate karyotypes (F1 and backcrosses) were discovered in central European Russia, and, for this reason, other studies have regarded obscurus and arvalis as conspecific. In the present study, to address the question of the species limits in the Al…

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…

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 …

Parental allocation of additional food to own health and offspring growth in a variable environment

2009

Life-history theory predicts increased investment in current reproduction when future reproduction is uncertain and a more balanced investment in current and future reproduction when prospects for both are good. The outcome of the balance in parental allocation depends on which life-history component maximizes the fitness benefits. In our study sys- tem, a 3-year vole cycle generates good prospects of current and future reproduction for Ural owls (Strix uralensis Pallas, 1771) in increase vole phases and uncertain prospects in decrease vole phases. We supplementary-fed Ural owls during the nestling period in 2002 (an increase phase) and 2003 (a decrease phase), and measured offspring growth…