Calleida viridipennis

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Calleida viridipennis
Calleida (Calleida) viridipennis (39447195934) (cropped).jpg
Scientific classification OOjs UI icon edit-ltr.svg
Domain: Eukaryota
Kingdom: Animalia
Phylum: Arthropoda
Class: Insecta
Order: Coleoptera
Family: Carabidae
Genus: Calleida
Species:
C. viridipennis
Binomial name
Calleida viridipennis
(Say, 1823)
Aerial photoshoot of Plummers Island, Maryland. Plum Island, aerial photograph.jpg
Aerial photoshoot of Plummers Island, Maryland.

The Calleida viridipennis is a species of ground beetle belonging to the Carabidae family, and are referred to as carabid beetles. It is found in various states, including New York, New Mexico, Louisiana, and Florida. [1] Habitat preferences include forests and swamps. [2] C. virdipennis is a particular carabid beetle that is, on average, 10 mm long. Recognizable by a green-black metallic exoskeleton, it has a trapezoidal head shape. [3] Its large eyes are also characteristic of the species. Below the exoskeleton reside functional wings, giving the beetle flight capacity. [4]

C. viridipennis is a spring breeder, rather than an autumn breeder. Therefore, they give rise to summer larvae and overwinter in the adult state. The female to male sex ratio does not differ significantly from the expected 1:1 ratio. [5]

Their diet consists of both animals and plants. C. viridipennis is a predator of the larva of the tortoise beetle, Hemisphaerota cyanea. [4] It is also a predator of the fruittree leafroller, Archipis argyrospila , caterpillar. [5] Within the carabid beetle species, food preferences are often linked to habitat preferences. [6]

Taxonomy

Calleida viridipennis is a carabid beetle, a type of ground beetle. This classification is given to all beetles in the Carabidae family, which belongs to the order Coleoptera. The body size of a carabid beetle is linked with habitat succession and stability. Carabid beetles feed on both animals and plants; however, broader mandibles suggest a preference for plants and seeds. Food preferences may also be linked with other characteristics such as body size or habitat preference. Species with larger eyes seem to prefer diurnal activity. C. viridipennis, having larger eyes, belongs to the diurnal subpopulation of carabid beetles. As a species-rich group, carabid beetles play important roles as bioindicators and mediators of nutrient flows in ecosystems. [6]

In 1932, 11 species of Calleida in the US and 177 species in the world had been recorded. [3]

The number of carabid species has dropped. A study conducted on Plummers Island, Maryland, which sampled ground beetles between 1901 and 1915, and then again in 1970 and 1978, found a decrease in species number. [7]

Distribution

The C. viridipennis beetle has a distribution that ranges from northern to southern America. The beetle has been observed to reside in southwestern New York to eastern Mexico, including southwestern Iowa. C. viridipennis has also been seen in Texas, Louisiana, and Florida. Research studies interested in investigating the predation of C. viridipennis have focused on the beetle populations found in Louisiana and Florida. Possible sightings of the beetle have been noted in Utah, Arizona, and California. It has also been found inhabiting Saint Martin, an island in the Caribbean. [1]

Genetic population structure

Comparison of Expected to Observed for a Chi Squared Goodness of Fit Test. Comparison of Expected to Observed for a Chi Squared Goodness of Fit Test.png
Comparison of Expected to Observed for a Chi Squared Goodness of Fit Test.

In having collected 146 adult C. viridipennis, researchers determined the sex ratio of females to males to be 1.1 to 1. [5]

Sex allocation refers to the allocation of resources to male and female production. Species may choose to manipulate the sex of their offspring to increase the fitness of the parents. While this would result in a skewed sex ratio biased towards one sex, Fisher’s Theory of Equal Investment maintains that a 1:1 ratio should be favored. The null hypothesis is that female and male offspring are equally costly to reproduce. [8]

The 1.1:1 ratio in the C. viridipennis beetle is also the evolutionary stable strategy (ESS). As described by Richard Dawkins, an evolutionary biologist who published The Selfish Gene , an ESS is a strategy that when adopted by most members of the population, it cannot be invaded by another strategy. [9]

Life cycle

The life cycle of a beetle consists of 4 different stages: egg, larval, pupal and adult. Carabid eggs are distributed among foliage and host webs. C. viridipennis is a spring beetle, thus larvae occur from late-March to early- or mid-October. Overwintering occurs in the adult state underneath tree bark. Conversely, autumn breeders lay eggs in the fall and overwinter in the larval stage. Adults survive approximately one year. [5]

Eggs

The length of the egg ranges between 1.0 and 1.3 mm. It is white to gray, and is oval shaped. The egg is enclosed in a purse that has been observed to be made of bark, silk, leaves, and grass. They are suspended from the leaves by a silk stalk. [10]

Larvae

The average length of the beetle larva is 7.99 to 14.11 mm long, and is characterized by its metallic black to green tergites. The head is trapezoidal and differs in color as it is yellow to reddish-brown. The antennae is composed of 4 segments. The mandibles are longer than the antennae. The widest part of the beetle are the thoracic segments. The beetle typically bears 4 blunt teeth. [10]

Pupa

The length measured from the crest of the head to the apex of the abdomen is recorded to be 6.6 to 7.7 mm. [10]

Habitat

Its habitat is characterized by open forests and swamps, which provide bark under which the beetle resides. [2] Adult beetles have been found under the bark of baldcypress, Taxodium distichum , and black willow, Salix nigra , at a height of more than 40 cm above the water level in forested wetlands. [5] Overwintering, the manner in which an insect passes the winter season, is done under tree bark. C. viridipennis will leave its habitat under the bark when the temperature is more suitable or food sources are more available. This occurs in late February or early March, which coincides with the activity of fruittree leafroller, Archips argyrospila , caterpillars. The beetle is a predator of the fruittree leafroller. [5]

Behavior

Overwintering

Overwintering is a characteristic behavior of the beetle. Beetles reside under bark in the adult stage, and emerge in late February or early March to begin breeding. Overwintering has been observed to coincide with the activity of prey. Thus, this behavior may be adopted to avoid low food resources, as well as avoid cold temperatures. [5]

The ability to overwinter requires physiological and behavioral adaptations. Cold temperatures may lead to the freezing of body fluids, which the beetle must be prepared to combat. Overwintering under bark is a behavioral adaptation to the cold temperatures. In addition, metabolic suppression serves to save energy reserves. [11]

Predation

C. viridipennis is a predator of the larva of the tortoise beetle, Hemisphaerota cyanea. Hemisphaerota cyanea P1010621a.jpg
C. viridipennis is a predator of the larva of the tortoise beetle, Hemisphaerota cyanea.

The beetle C. viridipennis is a predator of the larva of the tortoise beetle, Hemisphaerota cyanea . The larva constructs a thatch from fecal strands. As the larva grows, the thatch is enlarged. Production of the thatch begins when the larva hatches from the egg. Population occurs beneath the thatch. When fully constructed, the thatch completely conceals and physically shields that larva. It is a defense mechanism against predators. [4]

The physiology that allows for the making of the thatches by H. cyanea involves the accumulation of waste, which forms into a shield-like structure. This structure serves to take up feces, which is then emitted in strands. Larvae are capable of maneuvering the shield to face a certain direction. [4]

The mechanism by which the beetle feeds on the larva involves forcing itself beneath the thatch or chewing its way into it, as observed by researchers. Predation tests were conducted at the Archbold Biological Station in Florida. A beetle was placed in a Petri dish, along with 15 larvae over a period of 20 days. The larvae were all eaten. Observations included immediate attack upon contact with the thatch by the beetle. Researchers observed this behavior to be consistent, suggesting that predation of the larvae was a matter of routine. [4]

C. viridipennis is a predator of Archips argyrospila larva. Archips argyrospila larva.jpg
C. viridipennis is a predator of Archips argyrospila larva.

Researchers believe the physiology of the beetle is a potential explanation of its ability to circumvent the defense of the larvae. Due to its large eyes, agility, flight capacity, and diurnal feeding habits, it may have little difficulty in locating the larvae. [4] The ability to overcome the fecal shield may also be a result of its larger body size compared to other potential predators who have been unsuccessful in overcoming this particular defense mechanism. [12]

The beetle is also a known predator of the fruittree leafroller, Archips argyrospila , caterpillar. They are active on bald cypress trees. The emergence of the beetle from overwintering coincides with the activity of the caterpillar. [5]

Conservation Efforts

Vegetation of Plummers Island. Plummers Island Maryland.JPG
Vegetation of Plummers Island.

As observed on Plummers Island, the total carabid species number dropped between 1915 and 1970. [7] C. viridipennis is known to reside in this habitat. The decrease in species may reflect changes to the environment and the vegetation. [7] Further research has been conducted using carabid beetles to assess the effect of human-caused environmental changes. Researcher Jari Niemelä reviewed the effects of habitat fragmentation on carabid beetles. [13]

Fragmentation is defined as the breaking of a whole into many smaller remnants. This can alter the abundance and the species richness. Carabid beetles are threatened by habitat fragmentation. Conservation efforts may reduce the degree to which beetles are being threatened. [13]

Related Research Articles

<span class="mw-page-title-main">Beetle</span> Order of insects

Beetles are insects that form the order Coleoptera, in the superorder Holometabola. Their front pair of wings are hardened into wing-cases, elytra, distinguishing them from most other insects. The Coleoptera, with about 400,000 described species, is the largest of all orders, constituting almost 40% of described insects and 25% of all known animal species; new species are discovered frequently, with estimates suggesting that there are between 0.9 and 2.1 million total species. Found in almost every habitat except the sea and the polar regions, they interact with their ecosystems in several ways: beetles often feed on plants and fungi, break down animal and plant debris, and eat other invertebrates. Some species are serious agricultural pests, such as the Colorado potato beetle, while others such as Coccinellidae eat aphids, scale insects, thrips, and other plant-sucking insects that damage crops.

<span class="mw-page-title-main">Telephone-pole beetle</span> Species of beetle

The telephone-pole beetle is a beetle native to the eastern United States and the only living representative of the otherwise extinct family Micromalthidae. Larvae of the beetle live in decaying wood and can be pests to wooden structures, lending them their common name, the 'telephone-pole beetle.'

<span class="mw-page-title-main">Adephaga</span> Suborder of beetles

The Adephaga are a suborder of beetles, and with more than 40,000 recorded species in 10 families, the second-largest of the four beetle suborders. Members of this suborder are collectively known as adephagans. The largest family is Carabidae which comprises most of the suborder with over 40,000 species. Adephaga also includes a variety of aquatic beetles, such as predaceous diving beetles and whirligig beetles.

<span class="mw-page-title-main">Hydrophilidae</span> Family of beetles

Hydrophilidae, also known colloquially as water scavenger beetles, is a family of beetles. Aquatic hydrophilids are notable for their long maxillary palps, which are longer than their antennae. Several of the former subfamilies of Hydrophilidae have recently been removed and elevated to family rank; Epimetopidae, Georissidae, Helophoridae, Hydrochidae, and Spercheidae. While the majority of hydrophilids are aquatic, around a third of described species are terrestrial, mostly belonging to the subfamily Sphaeridiinae.

<span class="mw-page-title-main">Cleridae</span> Checkered beetles

Cleridae are a family of beetles of the superfamily Cleroidea. They are commonly known as checkered beetles. The family Cleridae has a worldwide distribution, and a variety of habitats and feeding preferences.

<i>Neocicindela tuberculata</i> Species of beetle

Neocicindela tuberculata is a species of tiger beetle in the family Cicindelidae, endemic to New Zealand. Its common names include common tiger beetle, moeone, and papapa, and in its laval stage penny doctor, butcher boy, kapuku, kui, kurikuri, moeone, and muremure. Neocicindela tuberculata was the first carabid beetle described from New Zealand. The species can run as fast as 5 miles per hour and are considered to be the fastest running beetles. Adult species prefer clay banks in summer and are good predators when in comes to insects.

<span class="mw-page-title-main">American carrion beetle</span> Species of beetle

The American carrion beetle is a North American beetle of the family Silphidae. It lays its eggs in, and its larvae consume, raw flesh and fungi. The larvae and adults also consume fly larvae and the larvae of other carrion beetles that compete for the same food sources as its larvae.

<i>Callosobruchus maculatus</i> Species of beetle

Callosobruchus maculatus is a species of beetles known commonly as the cowpea weevil or cowpea seed beetle. It is a member of the leaf beetle family, Chrysomelidae, and not a true weevil. This common pest of stored legumes has a cosmopolitan distribution, occurring on every continent except Antarctica. The beetle most likely originated in West Africa and moved around the globe with the trade of legumes and other crops. As only a small number of individuals were likely present in legumes carried by people to distant places, the populations that have invaded various parts of the globe have likely gone through multiple bottlenecks. Despite these bottlenecks and the subsequent rounds of inbreeding, these populations persist. This ability to withstand a high degree of inbreeding has likely contributed to this species’ prevalence as a pest.

<i>Archips semiferanus</i> Species of moth

Archips semiferanus is a species of moth in the family Tortricidae, and one of several species of moth commonly known as oak leafroller or oak leaf roller. The larvae feed on the leaves of oak trees in the eastern United States and southeastern Canada and are a major defoliator of oak trees, which can lead to tree mortality. In Pennsylvania in the late 1960s and early 1970s, oak leafrollers defoliated over 1,045,000 acres (423,000 ha).

<i>Lebia grandis</i> Species of beetle

Lebia grandis is a ground beetle in the family Carabidae found in North America. It is a specialist predator on the eggs and larvae of Colorado potato beetles, and its larvae are obligate parasitoids of Colorado potato beetle pupae.

<i>Broscus cephalotes</i> Species of beetle

Broscus cephalotes is a species of nocturnal, coastal ground beetle found throughout most of Europe. Its range spans from western Europe into western Siberia. The species was introduced recently in the eastern areas of Canada and has spread farther south and west into the United States. As a member of the family Carabidae, Broscus cephalotes is generally considered beneficial to humans due to its predatory habits. Their varied diet often includes crop pests and other small organisms.

<i>Archips goyerana</i> Species of moth

Archips goyerana, the baldcypress leafroller, is a moth of the family Tortricidae.

<i>Epomis</i> Subgenus of beetles

Epomis is a subgenus of ground beetle genus Chlaenius. The larvae of this subgenus are notable for being obligate role-reversal predators. Amphibians such as frogs are normally predators of beetles; however, Epomis larvae feed exclusively on amphibians.

<span class="mw-page-title-main">Fecal shield</span>

The fecal shield is a structure formed by the larvae of many species of beetles in the leaf beetle family, Chrysomelidae. It is composed of the frass of the insect and often its exuviae, or bits of shed exoskeleton. The beetle may carry the shield on its back or wield it upon its posterior end. The main function of the fecal shield is defense against predators. Other terms for the fecal shield noted in the literature include "larval clothing", "kotanhang", "faecal mask", "faecal pad", and "exuvio-faecal annex".

<i>Megadromus antarcticus</i> Species of beetle

Megadromus antarcticus, also known as the “Alexander beetle”, is a member of the Carabidae family and only found in the Canterbury region of New Zealand. Megadromus antarcticus are easily recognized by their iridescent green colouration.

<i>Chlaenius dejeanii</i> Species of beetle

Chlaenius dejeanii is a species of ground beetle native to the Palearctic and the Middle East. It is known from Bosnia and Herzegovina, Greece, Hungary, Israel, Italy, Russia, Syria, Turkey, and Ukraine.

<i>Pterostichus melanarius</i> Species of ground beetle

Pterostichus melanarius, the Rain Beetle, is a type of carabid of the genus Coleoptera. It is native to Europe but is increasingly found in North America after being introduced to the region in the 1920s. It is a predatory beetle that eats invertebrate pests, which makes it a valuable pest control agent in agricultural settings. Additionally, the beetle has wing dimorphism which has contributed to its increasing distribution across North America.

<i>Anisodactylus binotatus</i> Species of beetle

Anisodactylus binotatus is a species of ground beetle native to Europe. It was discovered as being introduced to Canterbury, New Zealand in 1938. Anisodactylus binotatus is a species of Carabidae, also known as the ground beetle family. Although this species of beetle has no official recorded common names, literature from England refers to it as the common shortspur beetle.

<i>Mecodema howitti</i> Species of beetle

Mecodema howitti, termed the Large Banks Peninsula ground beetle, is a carnivorous forest ground beetle in the genus Mecodema. It is endemic to Banks Peninsula, Canterbury, New Zealand, and is the largest of the 16 carabids found in the area.

<i>Rivacindela hudsoni</i> Species of beetle

Rivacindela hudsoni is an Australian species of the family Cicindelinae or "tiger beetle" and is the fastest running insect. The genus Rivacindela is contentiously treated as a subgenus of the broader Cicindela and are typically found in salty habitats such as dry salt lakes and salt streams. The species was discovered in South Australia and described in 1997, with an adult form of approximately 20–21mm in length and a running speed of 2.49m/s, or 120 body lengths per second.

References

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  3. 1 2 Zhou, Jianlin; Goyer, R. A. (1993). "Descriptions of the Immature Stages of Calleida viridipennis (Say) and Plochionus timidus Haldeman (Coleoptera: Carabidae: Lebiini)". The Coleopterists Bulletin. 47 (3): 233–242. ISSN   0010-065X. JSTOR   4009013.
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  9. Dawkins, Richard (1976). The Selfish Gene (3rd ed.). Oxford University Press. ISBN   0-19-857519-X.
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  11. Schebeck, Martin; Hansen, E. Matthew; Schopf, Axel; Ragland, Gregory J.; Stauffer, Christian; Bentz, Barbara J. (September 2017). "Diapause and overwintering of two spruce bark beetle species". Physiological Entomology. 42 (3): 200–210. doi:10.1111/phen.12200. ISSN   0307-6962. PMC   5599993 . PMID   28979060.
  12. Schenk, Dominique; Bacher, Sven (May 2002). "Functional response of a generalist insect predator to one of its prey species in the field". Journal of Animal Ecology. 71 (3): 524–531. Bibcode:2002JAnEc..71..524S. doi:10.1046/j.1365-2656.2002.00620.x. ISSN   0021-8790.
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Further reading