Scientific name

Chilocorus nigrita (Fabricius) [=Coccinella nigrita Fabricius, Chilocorus nigritus (Fabricius)]

This species is more commonly known in the literature as Chilocorus nigritus, which is incorrect. As per the rules of Zoological Nomenclature, the species name nigrita being a noun, does not change its ending when combined with Chilocorus, a generic name of different gender from the original genus, namely Coccinella (Grenstead, 1951; Booth, 1998).

Taxonomic position

Coleoptera: Coccinellidae: Chilocorinae: Chilocorini

Description

Length 3.2-4.0 mm; width 2.9-3.9 mm. Form subrounded, almost hemispherical and strongly convex. Head dull orange yellow. Pronotum dark pitchy brown to black in middle, paler on sides, anterolateral flaps orange yellow. Elytra black, shiny, with fine punctations. Ventral side including legs and inner margins of elytral epipleura orange yellow to yellowish brown, outer margins of epipleura pitchy brown to black. Male genitalia and female spermatheca as illustrated. Larva greyish, oval in outline with numerous spiny, branched protuberances on dorsal side.

Chilocorus subindicus Booth, a closely related species belonging to the nigrita-group of species, occurs together with C. nigrita in many parts of southern India, Lakshadweep Islands, etc., but is not as common. It is somewhat smaller in size and can be reliably separated from C. nigrita by the male genitalia.


Genitalia of Chilocorus nigrita: a-d. Male genitalia: a. Tegmen, lateral view; b. Tegmen, ventral view; c. sipho; d. siphonal apex; e. female spermatheca

Images

Chilocorus eggs  chilocorus grub  chilocorus pupa Fig. 1. Egg, Fig. 2. Larva, Fig. 3. Pupa
chilocorus adult  chilocorus adult Fig. 4, 5. Adult of C. nigrita

Distribution

India: Widely distributed (Andhra Pradesh; Assam; Goa; Karnataka; Kerala; Maharashtra; Orissa; Punjab; Tamil Nadu; Uttar Pradesh). Sri Lanka. Pakistan. Nepal. Myanmar. Malaysia. Chagos Archipelago. Indonesia. Madagascar. Reunion. Mauritius. Seychelles. Togo. Ghana. East Africa. Kenya. Tanzania. South Africa. Brazil.

It is a native of the Indian subcontinent and the most widespread species of this genus. It has been successfully introduced for the biological control of scale insects into, and naturally invaded, many different climatically appropriate regions of the world, including South America and Africa (Samways et al., 1999).

Prey / Associated habitat

Recorded on numerous hosts, mostly diaspine scales, infesting coffee, arecanut, coconut, citrus, neem, bamboo, mango, castor, brinjal, sugarcane, Morinda tinctoria, Nerium indicum, Cassia corymbosa, Thevetia, etc.

Specific host records are as follows: HEMIPTERA: Aleyrodidae: Aleurolobus barodensis (Maskell), Aleurodicus dispersus Russell. Aphididae: Aphis sp., Brachycaudus cardui (Linnaeus), Toxoptera citricida (Kirkaldy), indigo aphid. Coccoidea: Aonidiella aurantii (Maskell), Aonidiella citrina (Coquillett), Aonidiella orientalis (Newstead), Aonidiella simplex (Grp. & Charm) (=A. andersoni Laing), Aspidiotus destructor Signoret, A. nerii Bouche, Aspidiotus spp., Asterolecanium miliaris (Boisduval), Asterolecanium sp., Aulacaspis tegalensis (Zehntner), Aulacaspis tubercularis Newstead, Ceroplastes actiniformis Green, Ceroplastodes cajani (Maskell), Chionaspis sp., Chionaspis vitis Green, Chrysomphalus aonidum (Linnaeus) (=C. ficus Ashmead), Chrysomphalus dictyospermi (Morgan), Chrysomphalus pinnulifer diversicolor Green, Coccus colemani Kannan, Coccus hesperidum Linnaeus, Coccus viridis (Green), Diaspis bromeliae (Kerner), Diaspis echinocacti (Bouche), Drepanococcus chiton (Green), Eucalymnatus tessellatus (Signoret), Hemiberlesia lataniae (Signoret), Hsuia sp., Icerya seychellarum (Westwood), Ischnaspis longirostris (Signoret), Lepidosaphes beckii (Newman), Lepidosaphes (as Insulaspis) gloverii (Packard), Lepidosaphes sp., Megapulvinaria (as Pulvinaria) maxima (Green), Melanaspis glomerata (Green), Parasaissetia nigra (Nietner), Parlatoria blanchardi (Targioni Tozzetti), Parlatoria crypta McKenzie, Parlatoria orientalis Ramakrishna Ayyar, Parlatoria ziziphi (Lucas), Phoenicococcus marlatti Cockerell, Pinnaspis aspidistrae (Signoret), Pinnaspis buxi (Bouche), Pinnaspis dysoxyli (Maskell) (as Hemichionaspis minor Maskell), Pinnaspis strachani (Cooley), Palmicultor sp., Planococcus citri (Risso), Prococcus acutissimus (Green), Pseudaulacaspis cockerelli (Cooley), Pseudaulacaspis pentagona (Targioni Tozzetti), Pseudaulacaspis sp., Pseudococcus cryptus Hempel (=P. citriculus Green), Pseudococcus gilbertensis Beardsley, Pseudococcus sp., Pulvinaria psidii Maskell, Pulvinaria polygonata Cockerell, Pulvinaria spp., Diaspidiotus perniciosus (Comstock), Rastrococcus invadens Williams, Saccharicoccus sacchari (Cockerell), Selenaspidus articulatus (Morgan), Tecaspis sp., Vinsonia stellifera (Westwood). Psyllidae: Diaphorina citri Kuwayama, Trioza erytreae (Del Guercio).

Seasonal occurrence

Collected almost throughout the year in south India. Mass assemblages of overwintering or aestivating populations common on banyan trees, particularly during hot months (Tirumala Rao et al., 1954; Ketkar, 1959).

Natural enemies

Homalotylus mexicanus Timberlake, Homalotylus sp. (Hymenoptera: Encyrtidae).

Mass production and field release

Mass production is done on pumpkins infested with Hemiberlesia lataniae. This species has been used extensively for the control of scale insects on several hosts, particularly citrus, sugarcane, coconut, etc.

Sugarcane: Release in the form of egg pads @ 10 / spot in 100 spots per hectare. Citrus: Ten adults / tree.

References

  • Ahmad, R. 1970. Studies in West Pakistan on the biology of one nitidulid species and two coccinellid species (Coleoptera) that attack scale insects (Hom., Coccoidea). Bulletin of Entomological Research, 60: 5-16.
  • Booth, R.G. 1998. A review of the species resembling Chilocorus nigrita (Coleoptera: Coccinellidae): potential agents for biological control. Bulletin of Entomological Research, 88: 361-367.
  • Grenstead, L.W. 1951. A note on the trivial names nigrita and nigritus. Entomologist's Monthly Magazine, 87: 251-252.
  • Ketkar, S.M. 1959. Mass assemblage of the coccinellid beetle, Chilocorus nigritus Fabr. on banyan trees in Poona. Science & Culture 25: 273.
  • Nagaraja, H. & Hussainy, S.U. 1967. A study of six species of Chilocorus (Coleoptera: Coccinellidae) predaceous on San Jose and other scale insects. Oriental Insects, 1: 249-256.
  • Puttarudriah, M. & Channabasavanna, G.P. 1953. Beneficial coccinellids of Mysore-I. Indian Journal of Entomology, 15: 87-96.
  • Puttarudriah, M. & Channabasavanna, G.P. 1955. Beneficial coccinellids of Mysore-II. Indian Journal of Entomology, 17: 1-5.
  • Samways, M.J. 1984. Biology and economic value of the scale predator Chilocorus nigritus (F.). (Coccinellidae). Biocontrol News and Information, 5: 91-105.
  • Samways, M.J. 1989. Climate diagram and biological control: an example from the areography of the ladybird Chilocorus nigritus (Fabricius, 1798) (Insecta, Coleoptera, Coccinellidae). Journal of Biogeography, 16: 345-351.
  • Samways, M.J. & Wilson, S.J. 1988. Aspects of the feeding behaviour of Chilocorus nigritus (F.) (Col., Coccinellidae) relative to its effectiveness as a biocontrol agent. Journal of Applied Entomology, 106: 177-182.
  • Samways, M.J., Osborn, R., Hastings, H., Hattingh, V. 1999. Global climate change and accuracy of prediction of species' geographical ranges: establishment success of introduced ladybirds (Coccinellidae, Chilocorus spp.) worldwide. Journal of Biogeography, 26: 795-812.
  • Stebbing, E.P. 1903. Coleoptera 2. Notes upon the known predaceous Coccinellidae of the Indian region, Part I. Indian Museum Notes, VI(1): 47-62.
  • Tirumala Rao, V., David, A.L., Rao, K.R.M. 1954. Attempts at the utilisation of Chilocorus nigritus Fab. (Coleoptera, Coccinellidae) in the Madras State. Indian Journal of Entomology, 16: 205-209.