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It is generally accepted that the natural habitats of most pest insects can be found outside the synanthropic environment in layers of leaf litter, under bark, as well as in rodent or bird nests. Indeed, most of the common pests have been reported as being facultative nidicolous. Therefore infestation of commodities by pest insects out of these reservoirs is one considerable possibility. However, the likelihood of a pest´s occurrence and survival out-doors largely depends on its ecological potential and competitiveness against other species of the same ecological guild. Some pest species are rarely found in wild habitats, especially in those regions where they are not native and where they have been introduced by man. The fabric pest Tineola bisselliella serves as a good example. Most likely originating in Central or Southern Africa this insect was introduced into Europe probably not earlier than the late 18th century. Being more tolerant to dry environments than other fabric pests its economical importance increased during the 20th century when in-door climates changed because of central heating systems. Its occurrence in out-door natural habitats must be regarded as accidental. Reported founds of webbing clothes moth larvae in bird nests e.g. have been largely overstated in the literature. T. bisselliella should be regarded as an eusynanthropic species
The application of pheromone-baited traps to control pest insects in stored food or materials has become well established over the past decades. The main pheromone components of all major stored-product and material pests have been identified. Pest monitoring with pheromone traps is a key factor in integrated pest management to estimate population density build-ups and they may be used to define economic threshold levels. Male-attracting sex pheromones, e.g. for stored-product pyralids, the clothes moths, and some anobiid beetles, are especially effective in this aspect.
Monitoring pest population can facilitate optimal spatial and temporal control strategies, including efficacy evaluation of the implemented control measures. In addition to the sex pheromones, some beetles, such as grain and flour beetles, utilize aggregation pheromones, which attract both sexes.Implementation of these pheromones for mass trapping,which works well for the control of bark beetles in the forest environment, has been less successful for stored-product protection for various reasons and is thus not an established means of control.
When the monitoring tools are used in landscape areas, scrublands, forests, and away from anthropogenic influencedenvironments, natural reservoirs of a pest species and sources of new infestations can be identified. In addition to an economically driven adoption of pheromone traps, they may also provide information of a pest's general biology. Because stored-product and material pests must be considered neozoons in most parts of the world, their occurrence in natural habitats indicates a species' autecological capability to successfully compete with native species and to become faunistically established in non-synanthropic environments outside their zoogeographic origin. This review focuses on the use of pheromone traps for monitoring in outdoor situations.
A short natural and cultural history of the webbing clothes moth (Tineola bisselliella). It is generally accepted that the natural habitats of most pest insects can be found outside the synanthropic environment in layers of leaf litter, under bark, as well as in rodent or bird nests. Indeed, most of the common fabric pests have been reported as being facultative nidicolous. Therefore, infestation of commodities by pest insects out of these reservoirs is one possibility to be considered. However, the likelihood of a pest´s occurrence and survival outside of the synanthropic habitat largely depends on its ecological potential and competitiveness against other species of the same ecological guild. Some pest species are rarely found in wild habitats, especially in those regions where they are not native and where they have been introduced by man.
The fabric pest Tineola bisselliella serves as a good example. Most likely originating from Central or Southern Africa, this insect was introduced into Europe probably not earlier than the late 18th century. Being more tolerant to dry environments than other fabric pests, its economical importance increased during the 20th century when the indoor climate changed because of central heating systems. Its occurrence in outdoor natural habitats must be regarded as accidental. Reported finds of webbing clothes moth larvae in bird nests e. g. have been largely overstated in the literature. Tineola bisselliella should be regarded as an invasive and eusynanthropic species in most parts of the world.
Bacteria of the class Endomicrobia form a deepbranching clade in the Elusimicrobia phylum. They are found almost exclusively in the intestinal tract of animals and are particularly abundant in many termites, where they reside as intracellular symbionts in the cellulolytic gut flagellates. Although small populations of putatively free-living lineages have been detected in faunated and flagellate-free hosts, the evolutionary origin of the endosymbionts is obscured by the limited amount of phylogenetic information provided by the 16S rRNA gene fragment amplified with Endomicrobia-specific primers. Here, we present a robust phylogenetic framework based on the nearfull-length 16S–23S rRNA gene region of a diverse set of Endomicrobia from termites and cockroaches, which also allowed us to classify the shorter reads from previous studies. Our data revealed that endosymbionts arose independently at least four times
from different free-living lineages, which were already present in ancestral cockroaches but became associated with their respective hosts long after the digestive symbiosis between termites and flagellates had been established. Pyrotag sequencing revealed that the proportion of putatively free-living lineages increased, when all flagellates and their symbionts were removed from the gut of lower termites by starvation, starch feeding or hyperbaric oxygen, but results varied between different methods.
Permanente und nachhaltige Deckung von Grundbedürfnissen der Nahrungs- und Materialversorgung, aber auch das Ausnutzen von Arbeitshilfen, der Gebrauch von Versuchstieren in der Wissenschaft und die Freude an tierischer Begleitung in der Freizeit waren Beweggründe für die Domestikation von Tieren. Haustiere gehen auf eine zu ihrer Art gehörige Stammform einer Wildtierart zurück. Haustier und Wildtier sind somit Angehörige einer biologischen Spezies. Bei der Domestikation von Tieren spielte zwischenartliche Introgression keine Rolle. Die Domestikation von Haustieren durch Separation von kleinen Gruppen von Wildtieren erfolgte nur wenige Male an wenigen Orten (primäre Domestikationszentren). Haustiere bilden artübergreifend auffällig ähnliche morphologische und ethologische Merkmale aus (Domestikationssyndrom). Domestikation bei Wirbeltieren erfolgt primär über Selektion auf zutrauliches und zahmes Verhalten und unterliegt einem sehr komplexen pleiotropen Netzwerk von Regelkreisen. Die Domestikation ist ein koevolutiver Prozess und das Resultat eines bilateralen wechselseitigen Zusammenfindens von Prädispositionen und reziproken Valenzen der jeweiligen Partner von Haustier und Mensch.
Zahlreiche Insektenarten unter den Käfern und Schmetterlingen besitzen die ökologische Potenz, trockene Materialien pflanzlichen und tierischen Ursprungs als Nahrungs- und Brutsubstrat zu nutzen. Daher findet man diese Tiere auch an und in vom Menschen angelegten Nahrungsvorräten wie z. B. Getreidespeicher, an Kleidungs- und an Gebrauchsgegenständen aus Wolle, Pelzen oder Fellen sowie an oder in natürlichen Baumaterialien wie Holz. Aus wirtschaftlicher Sicht werden sie dann als Vorrats- bzw. Materialschädlinge bezeichnet.
Vorrats- und Materialschädlinge haben sehr ähnliche Lebensstrategien. Sie verfügen über eine breite Toleranz gegenüber abiotischen Umweltparametern und sind in der Regel Nahrungsopportunisten. Sie können längere Zeit ohne Nahrungsaufnahme überdauern und haben unter optimalen Bedingungen hohe Reproduktionsraten.
Es stellt sich die Frage, ob die auffälligen Anpassungen von Vorrats- und Materialschädlingen an einen menschennahen Lebensraum das Resultat von Prädispositionen und Selektion hin zu einem Lebensformtyp „Lager- oder Materialschädling“ sind, oder ob die synanthropen künstlichen (Öko)Systeme nur als überdimensionierte natürliche Reservoire fungieren.
Ökologische und ethologische Prädispositionen und Adaptationen sowie Verbreitungs- und Fortpflanzungsstrategien von Schadinsekten werden hier diskutiert, um phylogenetische und evolutionsbiologische Szenarien beim Übergang von ursprünglichen, also natürlichen Lebensräumen auf relativ jungzeitliche, von Menschen geprägte Habitate, zu rekonstruieren. Die angeführten Beispiele werden im kritischen Bezug zu publizierten Informationen über autökologische, faunistische sowie archäologische und historische Indizien über Ursprung und Ausbreitung von ausgewählten Schadinsekten (Hausbockkäfer, Textilmotten, Kornkäfer) begründet.