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|A female mosquito Culiseta longiareolata|
The mosquitoes are a family of small, midge-like flies: the Culicidae. Although a few species are harmless or even useful to humanity, most are a nuisance because they consume blood from living vertebrates, including humans. The females of many species of mosquitoes are blood-eating pests. In feeding on blood, some of them transmit extremely harmful human and livestock diseases, such as malaria, yellow fever and filariasis. Some authorities argue accordingly that mosquitoes are the most dangerous animals on Earth.
- 2 Life cycle
- 3 Feeding by adults
- 4 Distribution
- 5 Disease
- 6 Control
- 7 Evolution
- 8 Taxonomy of the Culicidae
- 9 References
- 10 Further reading
- 11 External links
Introduction[edit source | edit]Edit
Mosquitoes are members of a family of nematocerid flies: the Culicidae (from the Latin culex, genitive culicis, meaning "midge" or "gnat"). The word "mosquito" (formed by mosca and diminutive ito) is from the Spanish or Portuguese for "little fly". Superficially, mosquitoes resemble crane flies (family Tipulidae) and chironomid flies (family Chironomidae); as a result, casual observers seldom realize the important differences between the members of the respective families. In particular, the females of many species of mosquitoes are blood-eating pests and dangerous vectors of diseases, whereas members of the similar-looking Chironomidae and Tipulidae are not. Many species of mosquitoes are not blood eaters, and many of those that do create a "high to low pressure" in the blood to obtain it do not transmit disease. Also, in the bloodsucking species, only the females suck blood. Furthermore, even among mosquitoes that do carry important diseases, neither all species of mosquitoes, nor all strains of a given species transmit the same kinds of diseases, nor do they all transmit the diseases under the same circumstances; their habits differ. For example, some species attack people in houses, and others prefer to attack people walking in forests. Accordingly, in managing public health, knowing which species, even which strains, of mosquitoes with which one is dealing is important.
Over 3,500 species of mosquitoes have already been described from various parts of the world. Some mosquitoes that bite humans routinely act as vectors for a number of infectious diseases affecting millions of people per year. Others that do not routinely bite humans, but are the vectors for animal diseases, may become disastrous agents for zoonosis of new diseases when their habitats are disturbed, for instance by sudden deforestation.
Life cycle[edit source | edit]EditAnopheles larva from southern Germany, about 8 mm longAnatomy of a Culex larvaImage of pitcher plant mosquitoWyeomyia smithii, showing segmentation and partial anatomy of circulatory system
Like all flies, mosquitoes go through four stages in their lifecycles: egg, larva, pupa, and adult orimago. In most species, adult females lay their eggs in stagnant water; some lay eggs near the water's edge; others attach their eggs to aquatic plants. Each species selects the situation of the water into which it lays its eggs and does so according to its own ecological adaptations. Some are generalists and are not very fussy. Some breed in lakes, some in temporary puddles. Some breed in marshes, some in salt-marshes. Among those that breed in salt water, some are equally at home in fresh and salt water up to about one-third the concentration of seawater, whereas others must acclimatize themselves to the salinity. Such differences are important because certain ecological preferences keep mosquitoes away from most humans, whereas other preferences bring them right into houses at night.
Some species of mosquitoes prefer to breed in phytotelmata (natural reservoirs on plants), such as rainwater accumulated in holes in tree trunks, or in the leaf-axils of bromeliads. Some specialize in the liquid in pitchers of particular species of pitcher plants, their larvae feeding on decaying insects that had drowned there or on the associated bacteria; the genusWyeomyia provides such examples — the harmless Wyeomyia smithii breeds only in the pitchers of Sarracenia purpurea.
However, some species of mosquitoes that are adapted to breeding in phytotelmata are dangerous disease vectors. In nature, they might occupy anything from a hollow tree trunk to a cupped leaf. Such species typically take readily to breeding in artificial water containers, such as the odd plastic bucket, flowerpot "saucer", or discarded bottle or tire. Such casual puddles are important breeding places for some of the most serious disease vectors, such as species of Aedes that transmit dengue and yellow fever. Some with such breeding habits are disproportionately important vectors because they are well-placed to pick up pathogens from humans and pass them on. In contrast, no matter how voracious, mosquitoes that breed and feed mainly in remote wetlands and salt marshes may well remain uninfected, and if they do happen to become infected with a relevant pathogen, might seldom encounter humans to infect, in turn.
The first three stages—egg, larva, and pupa—are largely aquatic. These stages typically last five to 14 days, depending on the species and the ambient temperature, but there are important exceptions. Mosquitoes living in regions where some seasons are freezing or waterless spend part of the year in diapause; they delay their development, typically for months, and carry on with life only when there is enough water or warmth for their needs. For instance, Wyeomyia larvae typically get frozen into solid lumps of ice during winter and only complete their development in spring. The eggs of some species of Aedes remain unharmed in diapause if they dry out, and hatch later when they are covered by water.
Eggs hatch to become larvae, which grow until they are able to change into pupae. The adult mosquito emerges from the mature pupa as it floats at the water surface. Bloodsucking mosquitoes, depending on species, gender, and weather conditions, have potential adult lifespans ranging from as short as a week to as long as several months.
Eggs and oviposition[edit source | edit]EditAn egg raft of a Culex species, partly broken, showing individual egg shapes
Mosquito habits of oviposition, the ways in which they lay their eggs, vary considerably between species, and the morphologies of the eggs vary accordingly. The simplest procedure is that followed by many species of Anopheles; like many other gracile species of aquatic insects, females just fly over the water, bobbing up and down to the water surface and dropping eggs more or less singly. The bobbing behavior occurs among some other aquatic insects, as well, for example mayflies and dragonflies; it sometimes is called "dapping". The eggs of Anopheles species are roughly cigar-shaped and have floats down their sides. Females of many common species can lay 100–200 eggs during the course of the adult phase of their lifecycles. Even with high egg and intergenerational mortality, over a period of several weeks, a single successful breeding pair can create a population of thousands.
Some other species, for example members of the genus Mansonia, lay their eggs in arrays, attached usually to the under-surfaces of waterlily pads. Their close relatives, the genusCoquillettidia, lay their eggs similarly, but not attached to plants. Instead, the eggs form layers called "rafts" that float on the water. This is a common mode of oviposition, and most species of Culex are known for the habit, which also occurs in some other genera, such as Culiseta and Uranotaenia. Anopheles eggs may on occasion cluster together on the water, too, but the clusters do not generally look much like compactly glued rafts of eggs.
In species that lay their eggs in rafts, rafts do not form adventitiously; the female Culex settles carefully on still water with her hind legs crossed, and as she lays the eggs one by one, she twitches to arrange them into a head-down array that sticks together to form the raft.
Aedes females generally drop their eggs singly, much as Anopheles do, but not as a rule into water. Instead, they lay their eggs on damp mud or other surfaces near the water's edge. Such an oviposition site commonly is the wall of a cavity such as a hollow stump or a container such as a bucket or a discarded vehicle tire. The eggs generally do not hatch until they are flooded, and they may have to withstand considerable desiccation before that happens. They are not resistant to desiccation straight after oviposition, but must develop to a suitable degree first. Once they have achieved that, however, they can enter diapause for several months if they dry out. Clutches of eggs of the majority of mosquito species hatch as soon as possible, and all the eggs in the clutch hatch at much the same time. In contrast, a batch of Aedes eggs in diapause tends to hatch irregularly over an extended period of time. This makes it much more difficult to control such species than those mosquitoes whose larvae can be killed all together as they hatch. Some Anophelesspecies do also behave in such a manner, though not to the same degree of sophistication.
Larva[edit source | edit]EditMosquito larvae and pupa resting at water surface
Larvae breathe through spiracles located on their eighth abdominal segments, or through a siphon, so must come to the surface frequently. The larvae spend most of their time feeding on algae, bacteria, and other microbes in the surface microlayer. They dive below the surface only when disturbed. Larvae swim either through propulsion with their mouth brushes, or by jerky movements of their entire bodies, giving them the common name of "wigglers" or "wrigglers".
Pupa[edit source | edit]EditCulex larvae plus one pupaCulex larva and pupaAnatomy of an adult mosquito
As seen in its lateral aspect, the mosquito pupa is comma-shaped. The head and thorax are merged into a cephalothorax, with the abdomen curving around underneath. The pupa can swim actively by flipping its abdomen, and it is commonly called a "tumbler" because of its swimming action. As with the larvae, the pupae of most species must come to the surface frequently to breathe, which they do through a pair of respiratory trumpets on their cephalothoraces. However, pupae do not feed during this stage; typically they pass their time hanging from the surface of the water by their respiratory trumpets. If alarmed, say by a passing shadow, they nimbly swim downwards by flipping their abdomens in much the same way as the larvae do. If undisturbed, they soon float up again. After a few days or longer, depending on the temperature and other circumstances, the pupa rises to the water surface, the dorsal surface of its cephalothorax splits, and the adult mosquito emerges. The lower activity of the pupa compared to the larva is understandable, bearing in mind that it does not feed, whereas the larva feeds constantly.
Adult[edit source | edit]EditAdults of the yellow fever mosquitoAedes aegypti, a typical member of the subfamily Culicinae, the male is on the left, and females are on the right. Note the bushy antennae and longer palps in the male.
The period of development from egg to adult varies among species and is strongly influenced by ambient temperature. Some species of mosquitoes can develop from egg to adult in as few as five days, but a more typical period of development in tropical conditions would be some 40 days or more for most species. The variation of the body size in adult mosquitoes depends on the density of the larval population and food supply within the breeding water.
Adult mosquitoes usually mate within a few days after emerging from the pupal stage. In most species, the males form large swarms, usually around dusk, and the females fly into the swarms to mate.
Males typically live for about a week, feeding on nectar and other sources of sugar. After obtaining a full blood meal, the female will rest for a few days while the blood is digested and eggs are developed. This process depends on the temperature, but usually takes two to three days in tropical conditions. Once the eggs are fully developed, the female lays them and resumes host-seeking.
The cycle repeats itself until the female dies. While females can live longer than a month in captivity, most do not live longer than one to two weeks in nature. Their lifespans depend on temperature, humidity, and their ability to successfully obtain a blood meal while avoiding host defenses and predators.
Length of the adult varies, but is rarely greater than 16 mm (0.6 in), and weight up to 2.5 milligrams (0.04 grains). All mosquitoes have slender bodies with three segments: head, thorax and abdomen.
The head is specialized for receiving sensory information and for feeding. It has eyes and a pair of long, many-segmented antennae. The antennae are important for detecting host odors, as well as odors of breeding sites where females lay eggs. In all mosquito species, the antennae of the males in comparison to the females are noticeably bushier and contain auditory receptors to detect the characteristic whine of the females. The compound eyes are distinctly separated from one another. Their larvae only possess a pit-eye ocellus. The compound eyes of adults develop in a separate region of the head. New ommatidia are added in semicircular rows at the rear of the eye. During the first phase of growth, this leads to individual ommatidia being square, but later in development they become hexagonal. The hexagonal pattern will only become visible when the carapace of the stage with square eyes is molted. The head also has an elongated, forward-projecting, "stinger-like" proboscis used for feeding, and two sensory palps. The maxillary palps of the males are longer than their proboscises, whereas the females’ maxillary palps are much shorter. In typical bloodsucking species, the female has an elongated proboscis.
The thorax is specialized for locomotion. Three pairs of legs and a pair of wings are attached to the thorax. The insect wing is an outgrowth of the exoskeleton. The Anopheles mosquito can fly for up to four hours continuously at 1–2 km/h (0.6–1 mph), traveling up to 12 km (7.5 mi) in a night. Males beat their wings between 450 and 600 times per second.
The abdomen is specialized for food digestion and egg development; the abdomen of a mosquito can hold three times its own weight in blood. This segment expands considerably when a female takes a blood meal. The blood is digested over time, serving as a source of protein for the production of eggs, which gradually fill the abdomen.
Feeding by adults[edit source | edit]EditAedes aegypti, a common vector ofdengue fever and yellow fever
A mosquito has a variety of ways of finding their prey, including chemical, visual, and heat sensors. Typically, both male and female mosquitoes feed on nectar and plant juices, but in many species the mouthparts of the females are adapted for piercing the skin of animal hosts and sucking their blood as ectoparasites. In many species, the female needs to obtain nutrients from a blood meal before she can produce eggs, whereas in many other species, she can produce more eggs after a blood meal. Both plant materials and blood are useful sources of energy in the form of sugars, and blood also supplies more concentrated nutrients, such as lipids, but the most important function of blood meals is to obtain proteins as materials for egg production.
For females to risk their lives on blood sucking while males abstain is not a strategy limited to the mosquitoes; it also occurs in some other insect families, such as the Tabanidae. When a female reproduces without such parasitic meals, she is said to practiceautogenous reproduction, as in Toxorhynchites; otherwise, the reproduction may be termed anautogenous, as occurs in mosquito species that serve as disease vectors, particularly Anopheles and some of the most important disease vectors in the genus Aedes. In contrast, some mosquitoes, for example, many Culex, are partially anautogenous; they do not need a blood meal for their first cycle of egg production, which they produce autogenously; however, subsequent clutches of eggs are produced anautogenously, at which point their disease vectoring activity becomes operative.Here an Anopheles stephensi female is gorged with blood and beginning to pass unwanted liquid fractions of the blood to make room for more of the solid nutrients in her gut
With regard to host location, female mosquitoes hunt their blood host by detecting organic substances such as carbon dioxide (CO2) and 1-octen-3-ol produced from the host, and through optical recognition. Mosquitoes prefer some people over others. The preferred victim's sweat simply smells better than others because of the proportions of the carbon dioxide, octenol and other compounds that make up body odor. The most powerfulsemiochemical that triggers the keen sense of smell of Culex quinquefasciatus isnonanal. A large part of the mosquito’s sense of smell, or olfactory system, is devoted to sniffing out blood sources. Of 72 types of odor receptors on its antennae, at least 27 are tuned to detect chemicals found in perspiration. In Aedes, the search for a host takes place in two phases. First, the mosquito exhibits a nonspecific searching behavior until the perception of host stimulants, then it follows a targeted approach.
Most mosquito species are crepuscular (dawn or dusk) feeders. During the heat of the day, most mosquitoes rest in a cool place and wait for the evenings, although they may still bite if disturbed. Some species, such as the Asian tiger mosquito, are known to fly and feed during daytime.
Prior to and during blood feeding, blood-sucking mosquitoes inject saliva into the bodies of their source(s) of blood. This saliva serves as an anticoagulant; without it one might expect the female mosquito's proboscis to become clogged with blood clots. The saliva also is the main route by which mosquito physiology offers passenger pathogens access to the hosts' interior. Not surprisingly the salivary glands are a major target to most pathogens, whence they find their way into the host via the stream of saliva.
The bump left on the victim's skin after a mosquito bites is called a wheal, which is caused by histamines trying to fight off the protein left by the attacking insect.
Mosquitoes of the genus Toxorhynchites never drink blood. This genus includes the largest extant mosquitoes, the larvae of which prey on the larvae of other mosquitoes. These mosquito eaters have been used in the past as mosquito control agents, with varying success.
Mouthparts[edit source | edit]Edit
Mosquito mouthparts are very specialized, particularly those of the females, which in most species are adapted to piercing skin and then sucking blood. Apart from bloodsucking, the females generally also drink assorted fluids rich in dissolved sugar, such as nectar and honeydew, to obtain the energy they need. For this, their blood-sucking mouthparts are perfectly adequate. In contrast, male mosquitoes are not bloodsuckers; they only drink such sugary fluids as they can find. Accordingly, their mouthparts do not require the same degree of specialization as those of females.
Externally, the most obvious feeding structure of the mosquito is the proboscis. More specifically, the visible part of the proboscis is thelabium, which forms the sheath enclosing the rest of the mouthparts. When the mosquito first lands on a potential host, her mouthparts will be enclosed entirely in this sheath, and she will touch the tip of the labium to the skin in various places. Sometimes, she will begin to bite almost straight away, while other times, she will prod around, apparently looking for a suitable place. Occasionally, she will wander for a considerable time, and eventually fly away without biting. Presumably, this probing is a search for a place with easily accessible blood vessels, but the exact mechanism is not known. It is known that there are two taste receptors at the tip of the labium, which may well play a role.
The female mosquito does not insert her labium into the skin; it bends back into a bow when the mosquito begins to bite. The tip of the labium remains in contact with the skin of the victim, acting as a guide for the other mouthparts. In total, there are six mouthparts besides the labium: two mandibles, two maxillae, the hypopharynx, and the labrum.
The mandibles and the maxillae are used for piercing the skin. The mandibles are pointed, while the maxillae end in flat, toothed "blades". To force these into the skin, the mosquito moves its head backwards and forwards. On one movement, the maxillae are moved as far forward as possible. On the opposite movement, the mandibles are pushed deeper into the skin by levering against the maxillae. The maxillae do not slip back because the toothed blades grip the skin.
The hypopharynx and the labrum both are hollow. Saliva with anticoagulant is pumped down the hypopharynx to prevent clotting, and blood is drawn up the labrum.
To understand the mosquito mouthparts, it is helpful to draw a comparison with an insect that chews food, such as a dragonfly. A dragonfly has two mandibles, which are used for chewing, and two maxillae, which are used to hold the food in place as it is chewed. The labium forms the floor of the dragonfly's mouth, the labrum forms the top, while the hypopharynx is inside the mouth and is used in swallowing. Conceptually, then, the mosquito's proboscis is an adaptation of the mouthparts that occur in other insects. The labium still lies beneath the other mouthparts, but also enfolds them, and it has been extended into a proboscis. The maxillae still "grip" the "food" while the mandibles "bite" it. The top of the mouth, the labrum, has developed into a channeled blade the length of the proboscis, with a cross-section like an inverted "U". Finally, the hypopharynx has extended into a tube that can deliver saliva at the end of the proboscis. Its upper surface is somewhat flattened so, when pressed against it, the labrum forms a closed tube for conveying blood from the victim.
Saliva[edit source | edit]Edit
For the mosquito to obtain a blood meal, it must circumvent the vertebrate physiological responses. The mosquito, as with all blood-feeding arthropods, has mechanisms to effectively block the hemostasis system with their saliva, which contains a mixture of secreted proteins. Mosquito saliva negatively affects vascular constriction, blood clotting, platelet aggregation, angiogenesis and immunity, and creates inflammation. Universally, hematophagous arthropod saliva contains at least one anticlotting, one antiplatelet, and one vasodilatory substance. Mosquito saliva also contains enzymes that aid in sugar feeding and antimicrobial agents to control bacterial growth in the sugar meal. The composition of mosquito saliva is relatively simple, as it usually contains fewer than 20 dominant proteins. Despite the great strides in knowledge of these molecules and their role in bloodfeeding achieved recently, scientists still cannot ascribe functions to more than half of the molecules found in arthropod saliva. One promising application is the development of anticlotting drugs, such as clotting inhibitors and capillary dilators, that could be useful for cardiovascular disease.
It is now well recognized that feeding ticks, sandflies, and, more recently, mosquitoes, have an ability to modulate the immune response of the animals (hosts) on which they feed. The presence of this activity in vector saliva is a reflection of the inherent overlapping and interconnected nature of the host hemostatic and inflammatory/immunological responses and the intrinsic need to prevent these host defenses from disrupting successful feeding. The mechanism for mosquito saliva-induced alteration of the host immune response is unclear, but the data have become increasingly convincing that such an effect occurs. Early work described a factor in saliva that directly suppresses TNF-α release, but not antigen-induced histamine secretion, from activated mast cells.Experiments by Cross et al. (1994) demonstrated the inclusion of Ae. aegypti mosquito saliva into naïve cultures led to a suppression ofinterleukin (IL)-2 and IFN-γ production, while the cytokines IL-4 and IL-5 are unaffected by mosquito saliva. Cellular proliferation in response to IL-2 is clearly reduced by prior treatment of cells with SGE. Correspondingly, activated splenocytes isolated from mice fed upon by either Ae. aegypti or Cx. pipiens mosquitoes produce markedly higher levels of IL-4 and IL-10 concurrent with suppressed IFN-γ production. Unexpectedly, this shift in cytokine expression is observed in splenocytes up to 10 days after mosquito exposure, suggesting natural feeding of mosquitoes can have a profound, enduring, and systemic effect on the immune response.
T cell populations are decidedly susceptible to the suppressive effect of mosquito saliva, showing increased mortality and decreased division rates. Parallel work by Wasserman et al. (2004) demonstrated that T- and B-cell proliferation was inhibited in a dose dependent manner with concentrations as low as 1/7 of the saliva in a single mosquito. Depinay et al. (2005) observed a suppression of antibody-specific T cell responses mediated by mosquito saliva and dependent on mast cells and IL-10 expression.
A recent study suggests mosquito saliva can also decrease expression of interferon−α/β during early mosquito-borne virus infection.The contribution of type I interferons (IFN) in recovery from infection with viruses has been demonstrated in vivo by the therapeutic and prophylactic effects of administration of IFN-inducers or IFN, and recent research suggests mosquito saliva exacerbates West Nile virus infection, as well as other mosquito-transmitted viruses.
Egg development and blood digestion[edit source | edit]Edit
Female mosquitoes use two very different food sources. They need sugar for energy, which is taken from sources such as nectar, and they need blood as a source of protein for egg development. Because biting is risky and hosts may be difficult to find, mosquitoes take as much blood as possible when they have the opportunity. This, however, creates another problem. Digesting that volume of blood takes a while, and the mosquito will require energy from sugar in the meantime.
To avoid this problem, mosquitoes have a digestive system which can store both food types, and give access to both as they are needed. When the mosquito drinks a sugar solution, it is directed to a crop. The crop can release sugar into the stomach as it is required. At the same time, the stomach never becomes full of sugar solution, which would prevent the mosquito taking a blood meal if it had the chance.
Blood is directed straight into the mosquito's stomach. In species that feed on mammalian or avian blood, hosts whose blood pressure is high, the mosquito feeds selectively from active blood vessels, where the pressure assists in filling the gut rapidly. If, instead of slapping a feeding mosquito, one stretches one's skin so that it grips the proboscis and the mosquito cannot withdraw it, the pressure will distend the gut until it breaks and the mosquito dies.[better source needed] In the unmolested mosquito, however, the mosquito will withdraw, and as the gut fills up, the stomach lining secretes a peritrophic membrane that surrounds the blood. This membrane keeps the blood separate from anything else in the stomach. However, like certain other insects that survive on dilute, purely liquid diets, notably many of the Homoptera, many adult mosquitoes must excrete unwanted aqueous fractions even as they feed. (See the photograph of a feeding Anopheles stephensi: Note that the excreted droplet patently is not whole blood, being far more dilute). As long as they are not disturbed, this permits mosquitoes to continue feeding until they have accumulated a full meal of nutrient solids. As a result, a mosquito replete with blood can continue to absorb sugar, even as the blood meal is slowly digested over a period of several days. Once blood is in the stomach, the midgut of the female synthesizes proteolytic enzymes that hydrolyze the blood proteins into free amino acids. These are used as building blocks for the synthesis of egg yolk proteins.
In the mosquito Anopheles stephensi Liston, trypsin activity is restricted entirely to the posterior midgut lumen. No trypsin activity occurs before the blood meal, but activity increases continuously up to 30 hours after feeding, and subsequently returns to baseline levels by 60 hours. Aminopeptidase is active in the anterior and posterior midgut regions before and after feeding. In the whole midgut, activity rises from a baseline of approximately three enzyme units (EU) per midgut to a maximum of 12 EU at 30 hours after the blood meal, subsequently falling to baseline levels by 60 hours. A similar cycle of activity occurs in the posterior midgut and posterior midgut lumen, whereas aminopeptidase in the posterior midgut epithelium decreases in activity during digestion. Aminopeptidase in the anterior midgut is maintained at a constant, low level, showing no significant variation with time after feeding. Alpha-glucosidase is active in anterior and posterior midguts before and at all times after feeding. In whole midgut homogenates, alpha-glucosidase activity increases slowly up to 18 hours after the blood meal, then rises rapidly to a maximum at 30 hours after the blood meal, whereas the subsequent decline in activity is less predictable. All posterior midgut activity is restricted to the posterior midgut lumen. Depending on the time after feeding, greater than 25% of the total midgut activity of alpha-glucosidase is located in the anterior midgut. After blood meal ingestion, proteases are active only in the posterior midgut. Trypsin is the major primary hydrolytic protease and is secreted into the posterior midgut lumen without activation in the posterior midgut epithelium. Aminoptidase activity is also luminal in the posterior midgut, but cellular aminopeptidases are required for peptide processing in both anterior and posterior midguts. Alpha-glucosidase activity is elevated in the posterior midgut after feeding in response to the blood meal, whereas activity in the anterior midgut is consistent with a nectar-processing role for this midgut region.
Distribution[edit source | edit]EditFemale Ochlerotatus notoscriptusfeeding on a human arm, Tasmania, Australia
Mosquitoes are very widespread, occurring in all regions of the world except for Antarctica. In warm and humid tropical regions, they are active for the entire year, but in temperate regions, they hibernate over winter. Arctic mosquitoes may be active for only a few weeks as pools of water form on top of the permafrost. During that time, though, they exist in huge numbers and can take up to 300 ml of blood per day from each animal in a caribou herd.
Only Iceland does not have mosquitoes. 
Eggs from strains in the temperate zones are more tolerant to the cold than ones from warmer regions. They can even tolerate snow and subzero temperatures. In addition, adults can survive throughout winter in suitable microhabitats.
Means of dispersal[edit source | edit]Edit
Worldwide introduction of various mosquito species over large distances into regions where they are not indigenous has occurred through human agencies, primarily on sea routes, in which the eggs, larvae, and pupae inhabiting water-filled used tires and cut flowers are transported. However, apart from sea transport, mosquitoes have been effectively carried by personal vehicles, delivery trucks, trains, and aircraft. Man-made areas such as storm water retention basins, or storm drains also provide sprawling sanctuaries. Sufficient quarantine measures have proven difficult to implement.
Disease[edit source | edit]EditAnopheles albimanus mosquito feeding on a human arm – this mosquito is a vector of malaria, and mosquito control is a very effective way of reducing the incidence of malaria.Main articles: Mosquito-borne disease and Life-threatening disease
Mosquitoes can act as vectors for many disease-causing viruses and parasites. Infected mosquitoes carry these organisms from person to person without exhibiting symptoms themselves. Mosquito-borne diseases include:
- Viral diseases, such as yellow fever, dengue fever and chikungunya, transmitted mostly by Aedes aegypti. Dengue fever is the most common cause of fever in travelers returning from the Caribbean, Central America, and South Central Asia. This disease is spread through the bites of infected mosquitoes and cannot be spread person to person.
Severe dengue can be fatal, but with good treatment, less than 1% of patients die from dengue.
- The parasitic diseases collectively called malaria, caused by various species ofPlasmodium, carried by mosquitoes of the genus Anopheles
- Lymphatic filariasis (the main cause of elephantiasis) which can be spread by a wide variety of mosquito species
- West Nile virus is a concern in the United States, but there are no reliable statistics on worldwide cases.
- Eastern equine encephalitis virus is a concern in the eastern United States.
- Tularemia, a bacterial disease caused by Francisella tularensis, is variously transmitted, including by biting flies. Culex and Culisetaare vectors of tularemia, as well as arbovirus infections such as West Nile virus.
Potential transmission of HIV was originally a public health concern, but practical considerations and detailed studies of epidemiological patterns suggest that any transmission of the HIV virus by mosquitoes is at worst extremely unlikely.
Various species of mosquitoes are estimated to transmit various types of disease to more than 700 million people annually in Africa, South America, Central America, Mexico, Russia, and much of Asia, with millions of resultant deaths. At least two million people annually die of these diseases, and the morbidity rates are many times higher still.
Methods used to prevent the spread of disease, or to protect individuals in areas where disease is endemic, include:
- Vector control aimed at mosquito control or eradication
- Disease prevention, using prophylactic drugs and developing vaccines
- Prevention of mosquito bites, with insecticides, nets, and repellents
Since most such diseases are carried by "elderly" female mosquitoes, some scientists have suggested focusing on these to avoid the evolution of resistance.
Control[edit source | edit]EditMain article: Mosquito control
Many methods are used for mosquito control. Depending on the situation, the most important usually include:
- source reduction (e.g., removing stagnant water)
- biocontrol (e.g. importing natural predators such as dragonflies)
- trapping, and/or insecticides to kill larvae or adults
- exclusion (mosquito nets and window screening)
Source reduction[edit source | edit]EditWorld War II era pamphlet aimed to discourage creation of stagnant water
Source reduction means elimination of breeding places of mosquitoes. It includes engineering measures such as filling, leveling and drainage of breeding places, and water management (such as intermittent irrigation). Source reduction can also be done by making water unsuitable for mosquitoes to breed, for example, by changing salinity of water. Some specific measures are:
- For Culex: abolition of domestic and peridomestic sources of water suitable for breeding, for example removal and disposal of sewage and other waste water
- For Aedes: eliminating incidental containers such as discarded tins, crockery, pots, broken bottles, and coconut shells
- For Anopheles: abolish breeding places by filling or drainage
- For Mansonia: removal of aquatic plants manually or by application of herbicides
Details of the biology of different species of mosquitoes differ too widely for any limited set of rules to be sufficient in all circumstances. However, the foregoing are the most economical and practical measures for most purposes. The importance of peridomestic control arises largely because most species of mosquitoes rarely travel more than a few hundred meters unless the wind is favorable.
Exclusion[edit source | edit]Edit
In combination with scrupulous attention to control of breeding areas, window screens and mosquito nets are the most effective measures for residential areas. Insecticide-impregnated mosquito nets are particularly effective because they selectively kill those insects that attack humans, without affecting the general ecology of the area.
An ideal mosquito net is white in color (to allow easy detection of mosquitoes), rectangular, netted on sides and top, without a hole. The size of opening in net should not exceed 1.2 mm (0.05 in) in diameter, or about 23 holes per square centimeter (150 per square inch). Window screens should have copper or bronze gauze with 16 wires per inch.
Natural predators[edit source | edit]Edit
Dragonfly and damselfly nymphs and various other aquatic insect predators eat mosquitoes at all stages of development and dense populations can be useful in reducing mosquito problems. Various small fishes, such as species of Galaxias and members of thePoeciliidae, such as Gambusia (so-called mosquitofish) and guppies (Poecilia), eat mosquito larvae and sometimes may be worth introducing into ponds to assist in control. Many other types of fish are also known to consume mosquito larvae, including bass,bluegills, piranhas, Arctic char, salmon, trout, catfish, fathead minnows, goldfish, and killifish.
Although bats and purple martins can be prodigious consumers of insects, many of which are pests, less than 1% of their diets typically consist of mosquitoes. Neither bats nor purple martins are known to control or even significantly reduce mosquito populations.
Some cyclopoid copepods are predators on first-instar larvae, killing up to 40 Aedes larvae per day. Larvae of the non-bitingToxorhynchites mosquitoes also are natural predators of other Culicidae. Each larva can eat 10 to 20 mosquito larvae per day. During its entire development, a Toxorhynchites larva can consume an equivalent of 5,000 larvae of the first-instar (L1) or 300 fourth-instar larvae (L4). However, Toxorhynchites can consume all types of prey, organic debris, or even exhibit cannibalistic behavior.
Bacillus thuringiensis israelensis has also been used to control them as a biological agent.
Mosquito bites and treatment[edit source | edit]EditVideo of a mosquito biting on leg
Visible, irritating bites are due to an immune response from the binding of IgG and IgEantibodies to antigens in the mosquito's saliva. Some of the sensitizing antigens are common to all mosquito species, whereas others are specific to certain species. There are both immediate hypersensitivity reactions (types I and III) and delayed hypersensitivity reactions (type IV) to mosquito bites. Both reactions result in itching, redness and swelling. Immediate reactions develop within a few minutes of the bite and last for a few hours. Delayed reactions take around a day to develop, and last for up to a week. Severalanti-itch medications are commercially available, including those taken orally, such asBenadryl, or topically applied antihistamines and, for more severe cases, corticosteroids, such as hydrocortisone and triamcinolone.
Repellents[edit source | edit]EditMain article: Insect repellent
Insect repellents are applied on skin and give short-term protection against mosquito bites. The chemical DEET repels some mosquitoes and other insects. Some CDC-recommended repellents are picaridin, eucalyptus oil (PMD) and IR3535. Others are indalone, dimethyl pthalate, dimethyl carbate, and ethyl hexanediol.
Evolution[edit source | edit]Edit
The oldest known mosquito with an anatomy similar to modern species was found in 79-million-year-old Canadian amber from theCretaceous. An older sister species with more primitive features was found in amber that is 90 to 100 million years old. Two mosquito fossils have been found that show very little morphological change in modern mosquitoes against their counterpart from 46 million years ago.
Genetic analyses indicate the Culicinae and Anophelinae clades may have diverged about 150 million years ago. The Old and New World Anopheles species are believed to have subsequently diverged about 95 million years ago.
The mosquito Anopheles gambiae is currently undergoing speciation into the M(opti) and S(avanah) molecular forms. This means some pesticides that work on the M form will not work anymore on the S form.
Taxonomy of the Culicidae[edit source | edit]Edit
Over 3,500 species of the Culicidae have already been described. They are generally divided into two subfamilies which in turn comprise some 43 genera. These figures are subject to continual change, as more species are discovered, and as DNA studies compel rearrangement of the taxonomy of the family. The two main subfamilies are the Anophelinae and Culicinae, with their genera as shown in the subsection below.