An aggregated distribution, commonly found among predators and parasites, is a highly uneven (skewed) statistical distribution pattern in which they collect or aggregate in regions, which may be widely separated, where their prey or hosts are at high density. This distribution makes sampling difficult and invalidates commonly-used parametric statistics. A similar pattern is found among predators that search for their prey. [1]
When predators need to search for their prey, they could search at random, as has been assumed in models such as those made by Lotka in 1925 and Volterra in 1928. This would imply that they scatter themselves evenly across the environment. [1] However, prey may be concentrated at high densities in some areas and scarce elsewhere. The zoologists M. P. Hassell and R. M. May noted that predators and parasites, too, might aggregate themselves where prey was abundant, choosing some response curve: they observed for example that redshanks (predatory birds) adopted a sigmoid (s-shaped) response to the density of Corophium (amphipod) prey per square metre of mudflats. They noted, too, that several different behaviours of predators or parasites could cause them to aggregate selectively in areas where prey are at high density: they could be attracted by a volatile substance liberated by prey or the plants they are feeding on; they could choose to spend more time in areas where they have caught prey, as many predators appear to do; or, predators could follow an individual predator which had located prey, as is seen in feeding terns. Aggregated distributions of predators where they tend to spend time in areas where prey are concentrated have the effect of stabilising prey populations; when the time to travel between such concentrated areas is high; and when the prey populations too are more highly clumped. [1]
Parasite aggregation with respect to hosts is, according to Robert Poulin "a defining feature of metazoan parasite populations." [2] The main reason for this is probably either that some hosts are more exposed to parasites, or that they are more susceptible to them. [2] Aggregation is seen in directly transmitted parasites (those not using a vector) from many groups: ectoparasites like lice and mites, marine parasites like copepods and cyamid amphipods, and many kinds of nematode, fungi, protozoa, bacteria, and viruses. It is widespread, too, in trophically transmitted parasites of animals. The observed pattern is that most individual hosts are free or almost free of parasites, while a minority carry a large number of parasites. [3]
Aggregated distribution of parasites across their hosts poses considerable problems for students of parasite ecology, as it renders parametric statistics as commonly used by biologists invalid. Log-transformation of data before the application of parametric test, or the use of non-parametric statistics is recommended by several authors, but this can give rise to further problems, so quantitative parasitology is based on more advanced biostatistical methods. [4]
Parasitism is a close relationship between species, where one organism, the parasite, lives on or inside another organism, the host, causing it some harm, and is adapted structurally to this way of life. The entomologist E. O. Wilson characterised parasites as "predators that eat prey in units of less than one". Parasites include single-celled protozoans such as the agents of malaria, sleeping sickness, and amoebic dysentery; animals such as hookworms, lice, mosquitoes, and vampire bats; fungi such as honey fungus and the agents of ringworm; and plants such as mistletoe, dodder, and the broomrapes.
Predation is a biological interaction where one organism, the predator, kills and eats another organism, its prey. It is one of a family of common feeding behaviours that includes parasitism and micropredation and parasitoidism. It is distinct from scavenging on dead prey, though many predators also scavenge; it overlaps with herbivory, as seed predators and destructive frugivores are predators.
In ecology, a niche is the match of a species to a specific environmental condition. It describes how an organism or population responds to the distribution of resources and competitors and how it in turn alters those same factors. "The type and number of variables comprising the dimensions of an environmental niche vary from one species to another [and] the relative importance of particular environmental variables for a species may vary according to the geographic and biotic contexts".
In evolutionary biology, mimicry is an evolved resemblance between an organism and another object, often an organism of another species. Mimicry may evolve between different species, or between individuals of the same species. Often, mimicry functions to protect a species from predators, making it an anti-predator adaptation. Mimicry evolves if a receiver perceives the similarity between a mimic and a model and as a result changes its behaviour in a way that provides a selective advantage to the mimic. The resemblances that evolve in mimicry can be visual, acoustic, chemical, tactile, or electric, or combinations of these sensory modalities. Mimicry may be to the advantage of both organisms that share a resemblance, in which case it is a form of mutualism; or mimicry can be to the detriment of one, making it parasitic or competitive. The evolutionary convergence between groups is driven by the selective action of a signal-receiver or dupe. Birds, for example, use sight to identify palatable insects and butterflies, whilst avoiding the noxious ones. Over time, palatable insects may evolve to resemble noxious ones, making them mimics and the noxious ones models. In the case of mutualism, sometimes both groups are referred to as "co-mimics". It is often thought that models must be more abundant than mimics, but this is not so. Mimicry may involve numerous species; many harmless species such as hoverflies are Batesian mimics of strongly defended species such as wasps, while many such well-defended species form Müllerian mimicry rings, all resembling each other. Mimicry between prey species and their predators often involves three or more species.
The three-spined stickleback is a fish native to most inland and coastal waters north of 30°N. It has long been a subject of scientific study for many reasons. It shows great morphological variation throughout its range, ideal for questions about evolution and population genetics. Many populations are anadromous and very tolerant of changes in salinity, a subject of interest to physiologists. It displays elaborate breeding behavior and it can be social making it a popular subject of inquiry in fish ethology and behavioral ecology. Its antipredator adaptations, host-parasite interactions, sensory physiology, reproductive physiology, and endocrinology have also been much studied. Facilitating these studies is the fact that the three-spined stickleback is easy to find in nature and easy to keep in aquaria.
The blue mussel, also known as the common mussel, is a medium-sized edible marine bivalve mollusc in the family Mytilidae, the mussels. Blue mussels are subject to commercial use and intensive aquaculture. A species with a large range, empty shells are commonly found on beaches around the world.
A hyperparasite, also known as a metaparasite, is a parasite whose host, often an insect, is also a parasite, often specifically a parasitoid. Hyperparasites are found mainly among the wasp-waisted Apocrita within the Hymenoptera, and in two other insect orders, the Diptera and Coleoptera (beetles). Seventeen families in Hymenoptera and a few species of Diptera and Coleoptera are hyperparasitic. Hyperparasitism developed from primary parasitism, which evolved in the Jurassic period in the Hymenoptera. Hyperparasitism intrigues entomologists because of its multidisciplinary relationship to evolution, ecology, behavior, biological control, taxonomy, and mathematical models.
Parasite load is a measure of the number and virulence of the parasites that a host organism harbours. Quantitative parasitology deals with measures to quantify parasite loads in samples of hosts and to make statistical comparisons of parasitism across host samples.
Spatial ecology studies the ultimate distributional or spatial unit occupied by a species. In a particular habitat shared by several species, each of the species is usually confined to its own microhabitat or spatial niche because two species in the same general territory cannot usually occupy the same ecological niche for any significant length of time.
In statistics, overdispersion is the presence of greater variability in a data set than would be expected based on a given statistical model.
Species distribution, or speciesdispersion, is the manner in which a biological taxon is spatially arranged. The geographic limits of a particular taxon's distribution is its range, often represented as shaded areas on a map. Patterns of distribution change depending on the scale at which they are viewed, from the arrangement of individuals within a small family unit, to patterns within a population, or the distribution of the entire species as a whole (range). Species distribution is not to be confused with dispersal, which is the movement of individuals away from their region of origin or from a population center of high density.
Pomphorhynchus laevis is an endo-parasitic acanthocephalan worm, with a complex life cycle, that can modify the behaviour of its intermediate host, the freshwater amphipod Gammarus pulex. P. laevis does not contain a digestive tract and relies on the nutrients provided by its host species. In the fish host this can lead to the accumulation of lead in P. laevis by feeding on the bile of the host species.
In population ecology, density-dependent processes occur when population growth rates are regulated by the density of a population. This article will focus on density dependence in the context of macroparasite life cycles.
In biology, any group of fish that stay together for social reasons are shoaling, and if the group is swimming in the same direction in a coordinated manner, they are schooling. In common usage, the terms are sometimes used rather loosely. About one quarter of fish species shoal all their lives, and about one half shoal for part of their lives.
Coitocaecum parvum is a digeneic trematode or flatworm (Platyhelminthes) that is parasitic to the intestine of the common bully or upland bully. The common and upland bully are freshwater fish of New Zealand that C. parvum uses as its definitive host. C. parvum is a hermaphroditic freshwater trematode that can omit its definitive host and produce eggs by selfing or progenesis inside its amphipod second intermediate host
Gammarus lacustris is an aquatic amphipod.
Behavior-altering parasites are parasites with two or more hosts, capable of causing changes in the behavior of one of their hosts to enhance their transmission, sometimes directly affecting the hosts' decision-making and behavior control mechanisms. They do this by making the intermediate host, where they may reproduce asexually, more likely to be eaten by a predator at a higher trophic level which becomes the definitive host where the parasite reproduces sexually; the mechanism is therefore sometimes called parasite increased trophic facilitation or parasite increased trophic transmission. Examples can be found in bacteria, protozoa, viruses, and animals. Parasites may also alter the host behaviour to increase protection of the parasites or their offspring; the term bodyguard manipulation is used for such mechanisms.
Pleistophora mulleri (Pfeiffer) Georgev. 1929 is a parasite of the amphipod Gammarus duebeni celticus. The parasite targets the freshwater shrimp species and has shown higher rates of cannibalism, which in turn, affects biological communities and ecology.
Harrison's rule is an observation in evolutionary biology by Launcelot Harrison which states that in comparisons across closely related species, host and parasite body sizes tend to covary positively.
Disease ecology is a sub-discipline of ecology concerned with the mechanisms, patterns, and effects of host-pathogen interactions, particularly those of infectious diseases. For example, it examines how parasites spread through and influence wildlife populations and communities. By studying the flow of diseases within the natural environment, scientists seek to better understand how changes within our environment can shape how pathogens, and other diseases, travel. Therefore, diseases ecology seeks to understand the links between ecological interactions and disease evolution. New emerging and re-emerging infectious diseases are increasing at unprecedented rates which can have lasting impacts on public health, ecosystem health, and biodiversity.