Scale insect

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Scale insect
Temporal range: TriassicRecent
Wax Scale.jpg
Waxy scales on cycad leaf
Scientific classification Red Pencil Icon.png
Kingdom: Animalia
Phylum: Arthropoda
Class: Insecta
Order: Hemiptera
Suborder: Sternorrhyncha
Infraorder: Coccomorpha
Heslop-Harrison, 1952
Superfamily: Coccoidea
Handlirsch, 1903  [1]

See text

Scale insects are small insects of the order Hemiptera, suborder Sternorrhyncha. Of dramatically variable appearance and extreme sexual dimorphism, they comprise the infraorder Coccomorpha which is considered a more convenient grouping than the superfamily Coccoidea due to taxonomic uncertainties. Adult females typically have soft bodies and no limbs, and are concealed underneath domed scales, extruding quantities of wax for protection. Some species are hermaphroditic, with a combined ovotestis instead of separate ovaries and testes. Males, in the species where they occur, have legs and sometimes wings, and resemble small flies. Scale insects are herbivores, piercing plant tissues with their mouthparts and remaining in one place, feeding on sap. The excess fluid they imbibe is secreted as honeydew on which sooty mold tends to grow. The insects often have a mutualistic relationship with ants, which feed on the honeydew and protect them from predators. There are about 8,000 described species.


Scale insects appeared in the Triassic, before their modern food plants, the angiosperms, had evolved; early forms probably fed on gymnosperms. They became widespread and common in the Cretaceous, and are well represented in the fossil record, usually preserved in amber where they are sometimes associated with ants. Their closest relatives are the jumping plant lice, whiteflies, phylloxera bugs and aphids. The majority of female scale insects remain in one place as adults, with newly hatched nymphs, known as "crawlers", being the only mobile life stage, apart from the short-lived males. The reproductive strategies of many species include at least some amount of asexual reproduction by parthenogenesis.

Some scale insects are serious commercial pests, notably the cottony cushion scale ( Icerya purchasi ) on Citrus fruit trees; they are difficult to control as the scale and waxy covering protect them effectively from contact insecticides. Some species are used for biological control of pest plants such as the prickly pear, Opuntia . Others produce commercially valuable substances including carmine and kermes dyes, and shellac lacquer. The two red colour-names crimson and scarlet both derive from the names of Kermes products in other languages.


Armoured scale insects:(A) Lepidosaphes gloverii, adult females. (B) Parlatoria oleae, adult females (circular, with dark spot) and immatures (oblong). (C) Diaspidiotus juglansregiae, adult female walnut scale with waxy scale cover removed. Armored scale insects.png
Armoured scale insects:(A) Lepidosaphes gloverii, adult females. (B) Parlatoria oleae, adult females (circular, with dark spot) and immatures (oblong). (C) Diaspidiotus juglansregiae, adult female walnut scale with waxy scale cover removed.

Scale insects vary dramatically in appearance, from very small organisms (1–2 mm) that grow beneath wax covers (some shaped like oysters, others like mussel shells), to shiny pearl-like objects (about 5 mm), to animals covered with mealy wax. Adult females are almost always immobile (apart from mealybugs) and permanently attached to the plant on which they are feeding. They secrete a waxy coating for defence, making them resemble reptilian or fish scales, and giving them their common name. [2] The key character that sets apart the Coccomorpha from all other Hemiptera is the single segmented tarsus on the legs with only one claw at the tip. [3]

The group is extremely sexually dimorphic; female scale insects, unusually for Hemiptera, retain the immature external morphology even when sexually mature, a condition known as neoteny. Adult females are pear-shaped, elliptical or circular, with no wings, and usually no constriction separating the head from the body. Segmentation of the body is indistinct, but may be indicated by the presence of marginal bristles. Legs are absent in the females of some families, and when present vary from single segment stubs to five-segmented limbs. Female scale insects have no compound eyes, but ocelli (simple eyes) are sometimes present in Margarodidae, Ortheziidae and Phenacoleachiidae. The family Beesoniidae lacks antennae, but other families possess antennae with from one to thirteen segments. The mouthparts are adapted for piercing and sucking. [2]

Adult males in contrast have the typical head, thorax and abdomen of other insect groups, and are so different from females that pairing them as a species is challenging. They are usually slender insects resembling aphids or small flies. They have antennae with nine or ten segments, compound eyes (Margarodidae and Ortheziidae) or simple eyes (most other families), and legs with five segments. Most species have wings, and in some, alternate generations may be winged or wingless. Adult males do not feed, and die within two or three days of emergence. [2]

In species with winged males, generally only the forewings are fully functional. This is unusual among insects; it most closely resembles the situation in the true flies, the Diptera. However, the Diptera and Hemiptera are not closely related, and do not closely resemble each other in morphology; for example, the tail filaments of the Coccomorpha do not resemble anything in the morphology of flies. The hind (metathoracic) wings are reduced, commonly to the point that they can easily be overlooked. In some species the hind wings have hamuli, hooklets, that couple the hind wings to the main wings, as in the Hymenoptera. The vestigial wings are often reduced to pseudo-halteres, club-like appendages, but these are not homologous with the control organs of Diptera, and it is not clear whether they have any substantial control function. [4]

Hermaphroditism is very rare in insects, but several species of Icerya exhibit an unusual form. The adult possesses an ovotestis, consisting of both female and male reproductive tissue, and sperm is transmitted to the young for their future use. The fact that a new population can be founded by a single individual may have contributed to the success of the cottony cushion scale which has spread around the world. [5]

Life cycle

Life-cycle of the apple scale, Mytilaspis pomorum. a) underside of scale showing female and eggs, x24 b) scale upperside, x24 c) female scales on twig d) male scale, x12 e) male scales on twig EB1911 Hemiptera - Fig. 13.--Apple Scale Insect (Mytilaspis pomorum).jpg
Life-cycle of the apple scale, Mytilaspis pomorum. a) underside of scale showing female and eggs, x24 b) scale upperside, x24 c) female scales on twig d) male scale, x12 e) male scales on twig

Female scale insects in more advanced families develop from the egg through a first instar (crawler) stage and a second instar stage before becoming adult. In more primitive families there is an additional instar stage. Males pass through a first and second instar stage, a pre-pupal and a pupal stage before adulthood. [2]

The first instars of most species of scale insects emerge from the egg with functional legs, and are informally called "crawlers". They immediately crawl around in search of a suitable spot to settle down and feed. In some species they delay settling down either until they are starving, or until they have been blown away by wind onto what presumably is another plant, where they may establish a new colony. There are many variations on such themes, such as scale insects that are associated with species of ants that act as herders and carry the young ones to protected sites to feed. In either case, many such species of crawlers, when they moult, lose the use of their legs if they are female, and stay put for life. Only the males retain legs, and in some species wings, and use them in seeking females. To do this they usually walk, as their ability to fly is limited, but they may get carried to new locations by the wind. [2]

Apple scale. a) male, with legs and wings b) foot of male c) larva, x20 d) antenna of larva e) immobile female (removed from scale) EB1911 Hemiptera - Fig. 12.--Apple Scale Insect.jpg
Apple scale. a) male, with legs and wings b) foot of male c) larva, x20 d) antenna of larva e) immobile female (removed from scale)

Adult females of the families Margarodidae, Ortheziidae and Pseudococcidae are mobile and can move to other parts of the host plant or even adjoining plants, but the mobile period is limited to a short period between moults. Some of these overwinter in crevices in the bark or among plant litter, moving in spring to tender young growth. However, the majority of female scale insects are sedentary as adults. Their dispersal ability depends on how far a crawler can crawl before it needs to shed its skin and start feeding. There are various strategies for dealing with deciduous trees. On these, males often feed on the leaves, usually beside the veins, while females select the twigs. Where there are several generations in the year, there may be a general retreat onto the twigs as fall approaches. On branches, the underside is usually preferred as giving protection against predation and adverse weather. The solenopsis mealybug feeds on the foliage of its host in summer and the roots in winter, and large numbers of scale species feed invisibly, year-round on roots. [2]

Reproduction and the genetics of sex determination

Scale insects show a very wide range of variations in the genetics of sex determination and the modes of reproduction. Besides sexual reproduction, a number of different forms of reproductive systems are employed, including asexual reproduction by parthenogenesis. In some species, sexual and asexual populations are found in different locations, and in general, species with a wide geographic range and a diversity of plant hosts are more likely to be asexual. Large population size is hypothesized to protect an asexual population from becoming extinct, but nevertheless, parthenogenesis is uncommon among scale insects, with the most widespread generalist feeders reproducing sexually, the majority of these being pest species. [6]

A winged male Drosicha sp. Drosicha Lefroy.jpg
A winged male Drosicha sp.

Many species have the XX-XO system where the female is diploid and homogametic while the male is heterogametic and missing a sex chromosome. In some Diaspididae and Pseudococcidae, both sexes are produced from fertilized eggs but during development males eliminate the paternal genome and this system called paternal genome elimination (PGE) is found in nearly 14 scale insect families. This elimination is achieved with several variations. The commonest (known as the lecanoid system) involved deactivation of the paternal genome and elimination at the time of sperm production in males, this is seen in Pseudococcidae, Kerriidae and some Eriococcidae. In the other variant or Comstockiella system, the somatic cells have the paternal genome untouched. A third variant found in Diaspididae involves the paternal genome being completely removed at an early stage making males haploid both in somatic and germ cells even though they are formed from diploids, ie from fertilized eggs. In addition to this there is also true haplodiploidy with females born from fertilized eggs and males from unfertilized eggs. This is seen in the genus Icerya . In Parthenolecanium , males are born from unfertilized eggs but diploidy is briefly restored by fusion of haploid cleave nuclei and then one sex chromosome is lost through heterochromatinization. Females can reproduce parthenogenetically with six different variants based on whether males are entirely absent or not (obligate v. facultative parthenogenesis); the sex of fertilized v. unfertilized eggs; and based on how diploidy is restored in unfertilized eggs. The evolution of these systems are thought to be the result of intra-genomic conflict as well as possibly inter-genomic conflict with endosymbionts under varied selection pressures. The diversity of systems has made scale insects ideal models for research. [7]


A cluster of scale insects on a stem Scale Insects (2127992762).jpg
A cluster of scale insects on a stem

Scale insects are an ancient group, having originated in the Cretaceous, the period in which angiosperms came to dominance among plants, with only a few groups species found on gymnosperms. They feed on a wide variety of plants but are unable to survive long away from their hosts. While some specialise on a single plant species (monophagous), and some on a single genus or plant family (oligophagous), others are less specialised and feed on several plant groups (polyphagous). [2] The parasite biologist Robert Poulin notes that the feeding behaviour of scale insects closely resembles that of ectoparasites, living on the outside of their host and feeding only on them, even if they have not traditionally been so described; in his view, those species that remain immobile on a single host and feed only on it behave as obligate ectoparasites. [8] For example, cochineal species are restricted to cactus hosts, and the gall-inducing Apiomorpha are restricted to Eucalyptus . Some species have certain habitat requirements; some Ortheziidae occur in damp meadows, among mosses and in woodland soil, and the boreal ensign scale (Newsteadia floccosa) inhabits plant litter. [2] A Hawaiian mealybug Clavicoccus erinaceus that fed solely on the now critically endangered Abutilon sandwicense has gone extinct as has another species Phyllococcus oahuensis . [9] Several other monophagous scale insects, especially those on islands, are threatened by coextinction due to threats faced by their host plants. [10]

Most scale insects are herbivores, feeding on phloem sap drawn directly from the plant's vascular system, but a few species feed on fungal mats and fungi, such as some species in the genus Newsteadia in the family Ortheziidae. Plant sap provides a liquid diet which is rich in sugar and non-essential amino acids. In order to make up for the shortage of essential amino acids, they depend on endosymbiotic proteobacteria. [11] Scale insects secrete a large quantity of sticky viscid fluid known as "honeydew". This includes sugars, amino acids and minerals, and is attractive to ants as well as acting as a substrate on which sooty mould can grow. The mould can reduce photosynthesis by the leaves and detracts from the appearance of ornamental plants. The scale's activities can result in stress for the plant, causing reduced growth and giving it a greater susceptibility to plant diseases. [12]

Mutualistic Formica fusca ants tending a herd of mealybugs Formica fusca and mealy bugs.jpg
Mutualistic Formica fusca ants tending a herd of mealybugs

Scale insect in the genus Cryptostigma live inside the nests of neotropical ant species. [13] Many tropical plants need ants to survive which in turn cultivate scale insects thus forming a three-way symbiosis. [14] Some ants and scale insects have a mutualistic relationship; the ants feed on the honeydew and in return protect the scales. On a tulip tree, ants have been observed building a papery tent over the scales. In other instances, scale insects are carried inside the ant's nest; the ant Acropyga exsanguis takes this to an extreme by transporting a fertilised female mealybug with it on its nuptial flight, so that the nest it founds can be provisioned. [2] This provides a means for the mealybug to be dispersed widely. Species of Hippeococcus have long clinging legs with claws to grip the Dolichoderus ants which tend them; they allow themselves to be carried into the ant colony. Here the mealybugs are safe from predation and environmental hazards, while the ants have a source of nourishment. [2] Another species of ant maintains a herd of scale insects inside the hollow stems of a Barteria tree; the scale insects feed on the sap and the ants, while benefiting from the honeydew, drive away other herbivorous insects from the tree as well as preventing vines from smothering it. [15]

A ladybird preying on mealybugs Ladybug(india).jpg
A ladybird preying on mealybugs

Scale insects have various natural enemies, and research in this field is largely directed at the species that are crop pests. Entomopathogenic fungi can attack suitable scales and completely overgrow them. The identity of the host is not always apparent as many fungi are host-specific, and may destroy all the scales of one species present on a leaf while not affecting another species. [16] Fungi in the genus Septobasidium have a more complex, mutualistic relationship with scale insects. The fungus lives on trees where it forms a mat which overgrows the scales, reducing the growth of the individual parasitised scales and sometimes rendering them infertile, but protecting the scale colony from environmental conditions and predators. The fungus benefits by metabolising the sap extracted from the tree by the insects. [17]

Natural enemies include parasitoid wasps, mostly in the families Encyrtidae and Eulophidae, and predatory beetles such as fungus weevils, ladybirds and sap beetles. [2] Ladybirds feed on aphids and scale insects, laying their eggs near their prey to ensure their larvae have immediate access to food. The ladybird Cryptolaemus montrouzieri is known as the "mealybug destroyer" because both adults and larvae feed on mealybugs and some soft scales. [18] Ants looking after their providers of honeydew tend to drive off predators, but the mealybug destroyer has outwitted the ants by developing cryptic camouflage, with their larvae mimicking scale larvae. [2]


As pests

Many scale species are serious crop pests. [19] In 1990, they caused around $5 billion of damage to crops in the United States. [20] The waxy covering of many species of scale protects their adults effectively from contact insecticides, which are only effective against the first-instar nymph stage known as the crawler. However, scales can often be controlled using horticultural oils that suffocate them, systemic pesticides that poison the sap of the host plants, or by biological control agents such as tiny parasitoid wasps and ladybirds. Insecticidal soap may also be used against scales. [21]

One species, the cottony cushion scale, is a serious commercial pest on 65 families of woody plants, including Citrus fruits. It has spread worldwide from Australia. [22] [23]

As biological controls

At the same time, some kinds of scale insects are themselves useful as biological control agents for pest plants, such as various species of cochineal insects that attack invasive species of prickly pear, which spread widely especially in Australia and Africa. [24] [25]


Some types of scale insect are economically valuable for the substances they can yield under proper husbandry. Some, such as the cochineal, kermes, lac, Armenian cochineal, and Polish cochineal, have been used to produce red dyes for coloring foods and dyeing fabrics. [26] [27] [28] Both the colour name "crimson" and the generic name Kermes are from Italian carmesi or cremesi for the dye used for Italian silk textiles, in turn from the Persian [29] qirmizī (قرمز), meaning both the colour and the insect. [30] The colour name "scarlet" is similarly derived from Arabic siklāt, denoting extremely expensive luxury silks dyed red using kermes. [31]

Some waxy scale species in the genera Ceroplastes and Ericerus produce materials such as Chinese wax, [32] and several genera of lac scales produce shellac. [33]


The containing group of the scale insects was formerly treated as the superfamily Coccoidea but taxonomic uncertainties have led workers to prefer the use of the infraorder Coccomorpha as the preferred name for the group. [34] Scale insects are members of the Sternorrhyncha. The phylogeny of the extant groups, inferred from analysis of small subunit (18S) ribosomal RNA, is shown in the first cladogram. [35]


Psylloidea (jumping plant lice, etc) Psyllia pyricola.png

Aleyrodoidea (whiteflies) Neomaskellia bergii from CSIRO.jpg

Coccomorpha (scale insects) Ceroplastes ceriferus from CSIRO.jpg


Phylloxeroidea (phylloxera bugs) Daktulosphaira vitifoliae from CSIRO.jpg

Aphididae (aphids) Aphid winged.jpg

Fossil of the pseudococcid mealybug Electromyrmococcus (in the jaws of an ant) in Miocene Dominican amber Acropyga glaesaria SMFBE457B2 01.jpg
Fossil of the pseudococcid mealybug Electromyrmococcus (in the jaws of an ant) in Miocene Dominican amber

Phylogenetic diversification within the Coccomorpha has been analysed by the taxonomist Isabelle Vea and the entomologist David Grimaldi in 2016, combining DNA (3 gene regions) and 174 morphological characters (to allow fossil evidence to be incorporated). They showed that the main scale insect lineages diverged before their angiosperm hosts, and suggested that the insects switched from feeding on gymnosperms once the angiosperms became common and widespread in the Cretaceous. The Coccomorpha appeared at the start of the Triassic period, some 245 mya; the neococcoids some 185 mya. Scale insects are very well represented in the fossil record, being abundantly preserved in amber from the Early Cretaceous, 130 mya, onwards; they were already highly diversified by Cretaceous times. All the families were monophyletic except for the Eriococcidae. The Coccomorpha are division into two clades the "Archaeococcoids" and "Neococcoids". The archaeococcoid families have adult males with either compound eyes or a row of unicorneal eyes and have abdominal spiracles in the females. In neoccoids, the females have no abdominal spiracles. [37] In the cladogram below the genus Pityococcus is moved to the "Neococcoids". A cladogram showing the major families using this methodology is shown below. [38]




Matsucoccidae (pine bast scales)

Ortheziidae (ensign scales)

Margarodidae (ground pearls)




Monophlebidae (cottony cushion scales)





Putoidae (giant mealybugs)

Pseudococcidae (mealybugs)

Coccidae (soft scales)

Kermesidae (kermes dye scales)

Asterolecaniidae (pit scales)

Kerriidae (lac scales)

Dactylopiidae (cochineal insects)

Palaearctic "Eriococcidae" (felted scales)

Beesoniidae, Stictococcidae, part of "Eriococcidae"

Phoenicococcidae (palm scales)

Diaspididae (armoured scales)

+ Pityococcus

Recognition of scale insect families has fluctuated over time, and the validity of many remains in flux, [39] [40] with several recognized families not included in the phylogeny presented above including extinct groups are listed below: [41] [42] [43]

See also

Related Research Articles

Hemiptera Order of insects often called bugs

Hemiptera or true bugs are an order of insects comprising over 80,000 species within groups such as the cicadas, aphids, planthoppers, leafhoppers, bed bugs and shield bugs. They range in size from 1 mm (0.04 in) to around 15 cm (6 in), and share a common arrangement of sucking mouthparts. The name "true bugs" is often limited to the suborder Heteroptera. Many insects commonly known as "bugs", especially in American English, belong to other orders; for example, the lovebug is a fly and the May bug and ladybug are beetles.

Whitefly Family of insects

Whiteflies are Hemipterans that typically feed on the undersides of plant leaves. They comprise the family Aleyrodidae, the only family in the superfamily Aleyrodoidea. More than 1550 species have been described.

Mealybug Family of insects (Pseudococcidae)

Mealybugs are insects in the family Pseudococcidae, unarmored scale insects found in moist, warm habitats. Many species are considered pests as they feed on plant juices of greenhouse plants, house plants and subtropical trees and also act as a vector for several plant diseases. Some ants live in symbiotic relationships with them, protecting them from predators and feeding off the honeydew which they excrete.

Sternorrhyncha Order of true bugs

The Sternorrhyncha suborder of the Hemiptera contains the aphids, whiteflies, and scale insects, groups which were traditionally included in the now-obsolete order "Homoptera". "Sternorrhyncha" refers to the rearward position of the mouthparts relative to the head.

Margarodidae Family of true bugs

The Margarodidae or ground pearls are a family of scale insects within the superfamily Coccoidea. Members of the family include the Polish cochineal and Armenian cochineal and the original ground pearl genus, Margarodes. Beginning in 1880, a number of distinct subfamilies were recognized, with the giant coccids being the first. Although Maskell proposed a new family, many continued to regard the monophlebids as a mere subfamily for many years, and the Margarodidae classification continued to be polyphyletic through the 20th Century. Since then, taking the advice of Koteja several subfamilies and tribes have been elevated into their own families such as Matsucoccidae and Xylococcidae. The pared-down family of Margarodidae is monophyletic.


Trophobiosis is a symbiotic association between organisms where food is obtained or provided. The provider of food in the association is referred to as a trophobiont. The name is derived from the Greek τροφή trophē, meaning "nourishment" and -βίωσις -biosis which is short for the English symbiosis.

<i>Pseudococcus viburni</i> Species of true bug

Pseudococcus viburni is a close relative of the grape mealybug and a pest of the vineyards of New Zealand, the Central Coast of California, and the tea gardens of northern Iran. Unlike the grape mealybug, the obscure mealybug is not native to California, having most likely been introduced to the region from either Australia or South America in the latter part of the 19th century.

<i>Pheidole megacephala</i> Species of ant

Pheidole megacephala is a species of ant in the family Formicidae. It is commonly known as the big-headed ant in the USA and the coastal brown ant in Australia. It is a very successful invasive species and is considered a danger to native ants in Australia and other places. It has been nominated as one of the hundred "World's worst" invaders.

Putoidae is a family of scale insects commonly known as giant mealybugs or putoids. There is probably a single genus, Puto, containing about sixty species. The genus name Macrocerococcus has also been used but it is now considered to be a synonym of Puto. The genus Puto was formerly classified as a member of the Pseudococcidae; however, it so significantly differed from the rest of the Pseudococcidae that it was accorded its own family Putoidae.

<i>Paracoccus marginatus</i> Species of true bug

Paracoccus marginatus, commonly known as the papaya mealybug, is a small sap-sucking insect in the mealybug family, Pseudococcidae. It is found on a number of different hosts, including economically important tropical fruit trees and various ornamental plants.

<i>Callococcus</i> Genus of true bugs

Callococcus is a genus of Australian scale insect that feeds on species of Leptospermum, Hypocalymma, Kunzea and some other members of the tribes Chamelaucieae and Leptospermeae in the myrtle family Myrtaceae. Callococcus leptospermi induces stem-swelling galls on some species of Leptospermum, and it is considered to be a potential biological control agent of Leptospermum laevigatum in South Africa. The other described species of Callococcus do not induce galls.

<i>Planococcus citri</i> Species of true bug

Planococcus citri, commonly known as the citrus mealybug, is a species of mealybugs native to Asia. It has been introduced to the rest of the world, including Europe, the Americas, and Oceania, as an agricultural pest. It is associated with citrus, but it attacks a wide range of crop plants, ornamental plants, and wild flora.

<i>Dactylopius</i> Bugs, dye source, biocontrols, invasives

Dactylopius is a genus of insect in the superfamily Coccoidea, the scale insects. It is the only genus in the family Dactylopiidae. These insects are known commonly as cochineals, a name that also specifically refers to the best-known species, the cochineal. The cochineal is an insect of economic and historical importance as a main source of the red dye carmine. It has reportedly been used for this purpose in the Americas since the 10th century. Genus Dactylopius is also important because several species have been used as agents of biological pest control, and because several are known as invasive species.

Armenian cochineal Species of true bug

The Armenian cochineal, also known as the Ararat cochineal or Ararat scale, is a scale insect indigenous to the Ararat plain and Aras (Araks) River valley in the Armenian Highlands. It was formerly used to produce an eponymous crimson carmine dyestuff known in Armenia as vordan karmir and historically in Persia as kirmiz. The species is critically endangered within Armenia.

John Stuart Noyes is a Welsh entomologist.

Trabutina mannipara, or mana scale, is a species of mealybug found in the Middle East and southern Europe. It is the most well-known of the five species in the genus Trabutina, of which it is the type species, due to its association with the biblical story of manna. T. mannipara feeds parasitically on tamarisk trees, and excretes a sweet substance which is sometimes collected for human consumption. Obsolete terms for it include Coccus manniparus and Trabutina palestina. This species can be found in the Sinai and Iraq.

Trabutina is a genus of "blue-green" mealybugs, containing five species: T. crassispinosa, T. elastica, T. mannipara, T. serpentina, and T. tenax. This genus of scale insects feeds solely on plants of the genus Tamarix. Its type species is T. mannipara.

<i>Phenacoccus solenopsis</i> Species of true bug

Phenacoccus solenopsis, the cotton mealybug or solenopsis mealybug, is a species of mealybug in the family Pseudococcidae. Having originated in North America, it has spread to other parts of the world and become a major pest of cotton crops.

Geococcus coffeae is a species in the mealybug family, Pseudococcidae, commonly known as the coffee root mealybug, or brown scale. It lives underground where it inserts its mouthparts into roots and sucks the sap.

Newsteadia floccosa, the boreal ensign scale, is a species of scale insect in the family Ortheziidae. It is native to Europe and is found in the soil and amongst plant litter and mosses on the ground.


  1. "Coccoidea Handlirsch, 1903". Integrated Taxonomic Information System.
  2. 1 2 3 4 5 6 7 8 9 10 11 12 Capinera, John L. (2008). Encyclopedia of Entomology. Springer Science & Business Media. pp. 3263–3272. ISBN   978-1-4020-6242-1.
  3. Hodgson, Chris; Denno, Barb; Watson, Gillian W. (2021). "The Infraorder Coccomorpha (Insecta: Hemiptera)". Zootaxa. 4979 (1): 226–227. doi:10.11646/zootaxa.4979.1.24. ISSN   1175-5334.
  4. Dhooria, Manjit S. (2009). Ane's Encyclopedic Dictionary of General & Applied Entomology. Springer Science & Business Media. p. 198. ISBN   978-1-4020-8644-1.
  5. Gardner, A.; Ross, L. (2011). "The evolution of hermaphroditism by an infectious male-derived cell lineage: an inclusive-fitness analysis" (PDF). The American Naturalist. 178 (2): 191–201. doi:10.1086/660823. hdl: 11370/c2d17516-c096-4e53-80a1-d79b3aab10b3 . PMID   21750383.
  6. Ross, Laura; Hardy, Nate B.; Okusu, Akiko; Normark, Benjamin B. (2013). "Large population size predicts the distribution of sexuality in scale insects". Evolution. 67 (1): 196–206. doi: 10.1111/j.1558-5646.2012.01784.x . PMID   23289572.
  7. Ross, Laura; Pen, Ido; Shuker, David M. (2010). "Genomic Conflict in Scale Insects: the causes and consequences of bizarre genetic systems". Biological Reviews. 85 (4): 807–828. doi:10.1111/j.1469-185X.2010.00127.x. PMID   20233171. S2CID   13719072.
  8. Poulin, Robert (2011). Rollinson, D.; Hay, S. I. (eds.). The Many Roads to Parasitism: A Tale of Convergence. Advances in Parasitology. 74. Academic Press. pp. 27–28. doi:10.1016/B978-0-12-385897-9.00001-X. ISBN   978-0-12-385897-9. PMID   21295676.
  9. Moir, Melinda L.; Hughes, Lesley; Vesk, Peter A.; Leng, Mei Chen (2014). "Which host-dependent insects are most prone to coextinction under changed climates?". Ecology and Evolution. 4 (8): 1295–1312. doi:10.1002/ece3.1021. PMC   4020690 . PMID   24834327.
  10. Thacker, Jonathan I.; Hopkins, Graham W.; Dixon, Anthony F. G. (2006). "Aphids and scale insects on threatened trees: co-extinction is a minor threat". Oryx. 40 (2): 233–236. doi: 10.1017/S0030605306000123 . ISSN   0030-6053.
  11. Moran, Nancy A. (2001). "The coevolution of bacterial endosymbionts and phloem-feeding insects". Annals of the Missouri Botanical Garden. 88 (1): 35–44. doi:10.2307/2666130. ISSN   0026-6493. JSTOR   2666130.
  12. Stauffer, S.; Rose, M. (1997). Soft Scale Insects. Elsevier. pp. 186–187. ISBN   978-0-08-054135-8.
  13. Kondo, Takumasa; Gullan, Penny J. (2004). "A new species of ant-tended soft scale of the genus Cryptostigma Ferris (Hemiptera: Coccidae) associated with bamboo in Peru". Neotropical Entomology. 33 (6): 717–723. doi: 10.1590/S1519-566X2004000600009 .
  14. Itino, Takao; Murase, Kaori; Sato, Yumiko; Inamori, Keita; Itioka, Takao; Quek, Swee-Peck; Ueda, Shouhei (2008). "An ancient tripartite symbiosis of plants, ants and scale insects". Proceedings of the Royal Society B: Biological Sciences. 275 (1649): 2319–26. doi:10.1098/rspb.2008.0573. JSTOR   25249807. PMC   2603224 . PMID   18611850.
  15. Hölldobler, Bert; Wilson, Edward O. (1990). The Ants . Harvard University Press. p.  553. ISBN   978-0-674-04075-5.
  16. Evans, Harry C.; Hywel-Jones, Nigel L. (1997). Soft Scale Insects. Elsevier. pp. 3–4. ISBN   978-0-08-054135-8.
  17. "The genus Septobasidium". The genome portal of the Department of Energy Joint Genome Institute. Fungal Genomics Resource. Retrieved 18 January 2020.
  18. "Know Your Friends - Mealybug Destroyer". University of Wisconsin. 14 February 2009. Archived from the original on 12 April 2012. Retrieved 16 January 2020.
  19. "Scale Insects". Iowa State University. Retrieved 14 January 2020.
  20. Piper, Ross (2011). Pests: A Guide to the World's Most Maligned, Yet Misunderstood Creatures. ABC-CLIO. p. 149. ISBN   978-0-313-38426-4.
  21. "Scale insects". Gardeners' World . Retrieved 16 January 2020.
  22. ScaleNet
  23. Nair, K. S. S. (2007). Tropical Forest Insect Pests: Ecology, Impact, and Management. Cambridge University Press. p. 221. ISBN   9781139464857.
  24. Ramírez-Puebla, S. T. (2010). "Molecular phylogeny of the genus Dactylopius (Hemiptera: Dactylopiidae) and identification of the symbiotic bacteria" (PDF). Environmental Entomology. 39 (4): 1178–83. doi: 10.1603/EN10037 . PMID   22127169. S2CID   5816903. Archived from the original (PDF) on 2015-09-23.
  25. "Opuntia ficus-indica (prickly pear)". CABI. 3 January 2018.
  26. "Cochineal and Carmine". Major colourants and dyestuffs, mainly produced in horticultural systems. FAO. Retrieved June 16, 2015.
  27. "Guidance for Industry: Cochineal Extract and Carmine". FDA. Retrieved 6 July 2016.
  28. Munro, John H. (2003). Jenkins, David (ed.). Medieval Woollens: Textiles, Technology, and Organisation. The Cambridge History of Western Textiles. Cambridge University Press. pp. 214–215. ISBN   0-521-34107-8.
  29. ویکی, پارسی. "معنی قرمز | لغت نامه دهخدا". پارسی ویکی (in Persian). Retrieved 3 April 2021.
  30. "Crimson (n.)". Etymology Online. Retrieved 17 January 2020.
  31. Munro, John (2012). "Scarlet". In Gale Owen-Crocker; Elizabeth Coatsworth; Maria Hayward (eds.). Encyclopedia of Medieval Dress and Textiles. Brill. doi:10.1163/2213-2139_emdt_COM_550. ISBN   9789004124356.
  32. Zhang, Xiaoming (2011). Chinese Furniture. Cambridge University Press. p. 58. ISBN   978-0-521-18646-9.
  33. "How Shellac Is Manufactured". The Mail (Adelaide, SA : 1912 – 1954). 18 Dec 1937.
  34. Williams, Douglas J.; Hodgson, Chris J. (2014). "The case for using the infraorder Coccomorpha above the superfamily Coccoidea for the scale insects (Hemiptera: Sternorrhyncha)". Zootaxa. 3869 (3): 348. doi:10.11646/zootaxa.3869.3.9. ISSN   1175-5334.
  35. "Phylogeny of Insects". What-When-How. Retrieved 21 February 2018.
  36. Poinar, G.; Heiss, E. (2011). "New Termitaphididae and Aradidae (Hemiptera) in Mexican and Dominican amber" (PDF). Palaeodiversity. 4: 51–62.
  37. Williams, D. J.; Gullan, P. J.; Miller, D. R.; Matile-Ferrero, D.; Han, Sarah I. (2011). "A study of the scale insect genera Puto Signoret (Hemiptera: Sternorrhyncha: Coccoidea: Putoidae) and Ceroputo Šulc (Pseudococcidae) with a comparison to Phenacoccus Cockerell (Pseudococcidae)". Zootaxa. 2802 (1): 1. doi:10.11646/zootaxa.2802.1.1. ISSN   1175-5334.
  38. Vea, Isabelle M.; Grimaldi, David A. (2016). "Putting scales into evolutionary time: the divergence of major scale insect lineages (Hemiptera) predates the radiation of modern angiosperm hosts". Scientific Reports. 6 (1): 23487. Bibcode:2016NatSR...623487V. doi:10.1038/srep23487. ISSN   2045-2322. PMC   4802209 . PMID   27000526.
  39. Gullan, P. J.; Cook, L. G. (2007). "Phylogeny and higher classification of the scale insects (Hemiptera: Sternorrhyncha: Coccoidea)". Zootaxa. 1668: 413–425. doi:10.11646/zootaxa.1668.1.22.
  40. Hodgson, Chris J.; Hardy, Nate B. (2013). "The phylogeny of the superfamily Coccoidea (Hemiptera: Sternorrhyncha) based on the morphology of extant and extinct macropterous males". Systematic Entomology. 38 (4): 794–804. doi: 10.1111/syen.12030 .
  41. Szwedo, J. (2018). "The unity, diversity and conformity of bugs (Hemiptera) through time". Earth and Environmental Science Transactions of the Royal Society of Edinburgh. 107 (2–3): 109–128. doi:10.1017/s175569101700038x.
  42. Ben-Dov, Y.; Miller, D.R.; Gibson, G.A.P. "Home". ScaleNet. Archived from the original on 2013-04-04. Retrieved 2013-04-04.
  43. Johnson, Christine; Agosti, Donat; Delabie, Jacques H.; Dumpert, Klaus; Williams, D. J.; von Tschirnhaus, Michael; Maschwitz, Ulrich (2001). "Acropyga and Azteca ants (Hymenoptera: Formicidae) with scale insects (Sternorrhyncha: Coccoidea): 20 million years of intimate symbiosis". American Museum Novitates. 335: 1–18. doi:10.1206/0003-0082(2001)335<0001:AAAAHF>2.0.CO;2. ISSN   0003-0082.
  44. Poinar, G. O. Jr (2020). "Macrodrilidae fam. nov. (Hemiptera: Sternorrhyncha: Coccoidea), a new family of scale insects in mid-Cretaceous Burmese amber". Historical Biology: An International Journal of Paleobiology. in press: 1–5. doi:10.1080/08912963.2020.1733549.

Further references

On the University of Florida / Institute of Food and Agricultural Sciences Featured Creatures website: