Euwallacea perbrevis | |
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Scientific classification | |
Domain: | Eukaryota |
Kingdom: | Animalia |
Phylum: | Arthropoda |
Class: | Insecta |
Order: | Coleoptera |
Infraorder: | Cucujiformia |
Family: | Curculionidae |
Genus: | Euwallacea |
Species: | E. perbrevis |
Binomial name | |
Euwallacea perbrevis (Schedl, 1951) | |
Synonyms | |
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Euwallacea perbrevis, commonly known as tea shot-hole borer, is a species of weevil native to South and South-East Asia through to Australia, but introduced to Western countries. [1] [2]
It is native to American Samoa, Australia, Brunei, China, India, Fiji, Indonesia (Java), Papua New Guinea, Sri Lanka, Japan, Malaysia, Palau, Philippines, Réunion, Singapore, Taiwan, Timor, Vietnam and Thailand. It is also introduced into the United States, Hawaii, Costa Rica, and Panama. [3]
Body length is about 2.3 to 2.5 mm. [4] Elytral length is 1.42 to 1.68 mm. Pronotum length is 1.04 to 1.16 mm. Pronotum with 7 to 10 socketed denticles on the edge of the protibia. [5]
A polyphagous species, they are recorded from 16 genera in 13 families. [6] It generally inhabits under bark from dead tree, sapwood, tea stems, and large tree fall trunk. [5] The primary branches formed after pruning are more susceptible to attack. Adult females disperse during the day attacking hosts in a range 30–35 m. Females bore a bifurcated or simple tunnel in the twigs or branches. [7] In small plants, one or two branch tunnels are constructed. Egg-laying starts after completing the entrance tunnel. Then the matured female lays eggs singly or in small clusters. This egg production vary with climate and country, where the broods include about 15 to 20 individuals or sometimes 34 individuals. [8]
Number of males in the brood is very low, but they develop more rapidly than females. Males cannot fly and do not normally leave the parental gallery. However, males have observed to emerge and crawl on the surface of the bark. Sometimes, males enter to a gallery and mate with the females in that gallery system. Larvae usually live in the parental galleries. Female larvae pass through three instars. After final instar stage, the larvae pupate together in the tunnels. After emergence, the young females also remain in the galleries for several days. During this period, they undergo inbreeding where they are fertilized by their brothers. Mated females emerge through the original entrance tunnel and fly to new hosts. [8]
New generation emerge about 5 to 6 weeks after the host is infested. The egg, larval and pupal stages of the species lasted about 8 to 10, 21 to 26 and 10 to 12 days, respectively. It feeds on a symbiotic fungus that is cultivated in the xylem of woody plants. Adults generally stored and carry spores of the ambrosia fungus in mycangia. Ambrosia fungus includes: Fusarium bugnicourtii , Fusarium tumidum , Fusarium rekanum , Ceratocystis fimbriata and Graphium . [8] [9] [10]
Ambrosia beetles are beetles of the weevil subfamilies Scolytinae and Platypodinae, which live in nutritional symbiosis with ambrosia fungi. The beetles excavate tunnels in dead or stressed trees into which they introduce fungal gardens, their sole source of nutrition. After landing on a suitable tree, an ambrosia beetle excavates a tunnel in which it releases its fungal symbiont. The fungus penetrates the plant's xylem tissue, extracts nutrients from it, and concentrates the nutrients on and near the surface of the beetle gallery. Ambrosia fungi are typically poor wood degraders, and instead utilize less demanding nutrients. Symbiotic fungi produce and detoxify ethanol, which is an attractant for ambrosia beetles and likely prevents growth of antagonistic pathogens and selects for other beneficial symbionts. The majority of ambrosia beetles colonize xylem of recently dead trees, but some colonize stressed trees that are still alive, and a few species attack healthy trees. Species differ in their preference for different parts of trees, different stages of deterioration, and in the shape of their tunnels ("galleries"). However, the majority of ambrosia beetles are not specialized to any taxonomic group of hosts, unlike most phytophagous organisms including the closely related bark beetles. One species of ambrosia beetle, Austroplatypus incompertus exhibits eusociality, one of the few organisms outside of Hymenoptera and Isoptera to do so.
A bark beetle is the common name for the subfamily of beetles Scolytinae. Previously, this was considered a distinct family (Scolytidae), but is now understood to be a specialized clade of the "true weevil" family (Curculionidae). Although the term "bark beetle" refers to the fact that many species feed in the inner bark (phloem) layer of trees, the subfamily also has many species with other lifestyles, including some that bore into wood, feed in fruit and seeds, or tunnel into herbaceous plants. Well-known species are members of the type genus Scolytus, namely the European elm bark beetle S. multistriatus and the large elm bark beetle S. scolytus, which like the American elm bark beetle Hylurgopinus rufipes, transmit Dutch elm disease fungi (Ophiostoma). The mountain pine beetle Dendroctonus ponderosae, southern pine beetle Dendroctonus frontalis, and their near relatives are major pests of conifer forests in North America. A similarly aggressive species in Europe is the spruce ips Ips typographus. A tiny bark beetle, the coffee berry borer, Hypothenemus hampei is a major pest on coffee plantations around the world.
The term mycangium is used in biology for special structures on the body of an animal that are adapted for the transport of symbiotic fungi. This is seen in many xylophagous insects, which apparently derive much of their nutrition from the digestion of various fungi that are growing amidst the wood fibers. In some cases, as in ambrosia beetles, the fungi are the sole food, and the excavations in the wood are simply to make a suitable microenvironment for the fungus to grow. In other cases, wood tissue is the main food, and fungi weaken the defense response from the host plant.
Xyleborus glabratus, the redbay ambrosia beetle, is a type of ambrosia beetle invasive in the United States. It has been documented as the primary vector of Raffaelea lauricola, the fungus that causes laurel wilt, a disease that can kill several North American tree species in the family Lauraceae, including redbay, sassafras, and avocado.
Ips is a genus of beetles in the family Curculionidae, the true weevils. They are bark beetles, members of the subfamily Scolytinae. Species are distributed throughout the Northern Hemisphere. Some are known as introduced species in Australia and Africa. Many species are pests of forest trees, especially pines and spruces. They are known commonly as engraver beetles, ips engraver beetles, and pine engravers.
Euwallacea fornicatus, also known as tea shot-hole borer, or polyphagous shot-hole borer (PSHB) is a species complex consisting of multiple cryptic species of ambrosia beetles known as an invasive species in California, Israel, South Africa, and Australia. The species has also been unintentionally introduced into exotic greenhouses in several European countries.
Xylosandrus compactus is a species of ambrosia beetle. Common names for this beetle include black twig borer, black coffee borer, black coffee twig borer and tea stem borer. The adult beetle is dark brown or black and inconspicuous; it bores into a twig of a host plant and lays its eggs, and the larvae create further tunnels through the plant tissues. These beetles are agricultural pests that damage the shoots of such crops as coffee, tea, cocoa and avocado.
Xylosandrus crassiusculus, known generally as the Asian ambrosia beetle or granulate ambrosia beetle, is a species of tropical bark beetle in the family Curculionidae. It is native to Asia and has spread to Africa, Europe, Australasia and the Americas. The adult beetle is reddish-brown and some 2 to 3 mm long.
Xyleborus affinis, the sugarcane shot-hole borer, is a species of ambrosia beetle in the family Curculionidae. It is found on all continents with woodlands and is one of the most widespread ambrosia beetles internationally, primarily in areas with humid tropical climates like Florida. Like other ambrosia beetles, Xyleborus affinis is attracted to dead fallen logs in early stages of decay. Due to the presence of X. affinis on moist timber, this species is mistakenly believed to be the cause of tree death. However, there is insufficient evidence to support their presence as a causal factor. Rather, these beetles are believed to target and accelerate the decay process of trees that are already deteriorated and weak.
Xylosandrus germanus, known generally as the alnus ambrosia beetle or black stem borer, is a species of ambrosia beetle in the family Curculionidae. X. germanus poses challenges in woody ornamental species and orchard crops such as apples and pecan. Furthermore, X. germanus is recognized or suspected to act as a vector for plant pathogens to varying extents, potentially leading to the decline of trees. The black stem borer is native to eastern Asia, but is an invasive species in Europe and North America. This species carries and feeds on associated ambrosia fungus, Ambrosiella grosmanniae.
Xyleborinus saxesenii, commonly known as the fruit-tree pinhole borer, is a species of ambrosia beetle in the family Curculionidae. It is native to the Palaearctic region but has been introduced in many locations, including North America. X. saxesenii typically live in freshly dead wood, but it has also been reported to attack live trees. Such attacks on live trees may lead to economic damage.
Cnestus mutilatus, commonly known as the camphor shot borer, camphor shoot borer, or sweetgum ambrosia beetle, is a species of ambrosia beetle in the subfamily Scolytinae of the weevil family Curculionidae. It is native to Asia, but has been established as an invasive species in the United States since 1999.
Xyleborus dispar is a species of bark beetle commonly called the Pear blight beetle, or the European shothole borer. It is an invasive species in North America, and can be a pest in orchards and forests throughout its range.
Euwallacea interjectus is a species of Euwallacea fornicatus beetle native to Asia but has been introduced to the Western hemisphere over the last century.
Sueus niisimai is a species of weevil found in India, Sri Lanka, China, Japan, Taiwan, Korea, Malaysia and Indonesia. It is also found in Australia and Fiji, presumably introduced.
Xyleborus perforans, commonly known as island pinhole borer, is a species of weevil native in the Oriental region through to Australia but shows a cosmopolitan distribution due to introduction to many parts of the world.
Euwallacea similis, is a species of weevil native in the Oriental region through to Australia but shows a cosmopolitan distribution due to introduction to many parts of the world.
Ambrosiella roeperi is the fungal symbiont of the granulate ambrosia beetle, Xylosandrus crassiusculus, facilitating this insect’s capacity to accumulate on and damage a diverse array of woody plants from around the world. It is one of several important nutritional partners derived from order Microascales that sustain and are transported by xylomycetophagous scolytine beetles.
Euwallacea validus is a species of Euwallacea beetles native to Asia. The beetle species was discovered in Long Island, New York in 1975. Like other Euwallacea species beetles, E. validus is known for its mutualistic symbiotic relationship with fungi, acting as a vector for Fusarium oligoseptatum and Raffaelea subfusca, often using Tree of Heaven as a preferred host. Out of the five confirmed species of Euwallacea spp. in the United States, E. validus is the most widespread and longest established, yet much about their second fungal partner, Raffaelea subfusca, is not known.
Euwallacea is a genus of typical bark beetles in the family Curculionidae. They are commonly known as Ambrosia beetles, as all species are symbiotic with Ambrosia fungi. Originally from Asia or Wallacea, they are now found worldwide. Many species are pests, causing damage to, or the death of, tree species valued for their fruit or timber.