Host Plants, Geographical Distribution, Natural Enemies and Biological Studies of the Citrus Mealybug, Planococcus Citri (Risso) (Hemiptera: Pseudococcidae) Noha H
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New Records of Some Pests of the Coconut Inflorescence and Developing Fruit and Their Natural Enemies in Sri Lanka
COCOS, (1987) 5, 39—42 Printed in Sri Lanka New Records of some Pests of the Coconut Inflorescence and Developing Fruit and Their Natural Enemies in Sri Lanka L. C. P. FERNANDO and P. KANAGARATNAM Coconut Research Institute, Lunuwila, Sri Lanka. ABSTRACT A survey was carried out at Bandirippuwa Estate, Kirimetiyana Estate and at Isolated Seed Garden, Rajakadaluwa for the pests of coconut inflorescence and developing fruits. The mite, Dolichotetranychus sp. (Tenuipalpidae) which lives beneath the perianth and feeds on the epicarp, causes considerable damage to the developing fruit. Bi-monthly observations on the intensity of infestation of nuts among different forms of coconut indicated a significant difference among forms in their susceptibility to mite damage. Pseudococcus cocotis (Maskell) (Pseudococcidae), Pseudococcus citriculus Green (Pseudococcidae) and Planococcus lilacinus (Cockereli) (Pseudococcidae), when feeding in large numbers on the peduncle, cause button nut shedding and drying up of the inflo rescence. The parasitoids and predators of these mealybugs recorded for the first time in Sri Lanka are Promuscidea unfasciativentris Girault (Aphelinidae) Platygaster sp. (Platygastridae), Anagyrus sp. nr. pseudococci (Girault) (Encyrtidae) Coccodiplosis sp. (Cecidomyiidae), Cryptogonus bryanti Kapur (Coccinellidae) and Pseudoscymnus sp. (Coccinellidae). Several species of scale insects namely, Coccus hesperidum (Linnaeus) (Coccidae) Aulacaspis sp. (Diaspididae), Pseudaulacaspis cockerelli (Cooley) (Diaspididae), Aoni- diella orientalis (Newstead) (Diaspididae), and Pinnaspis strachani (Cooley) (Diaspididae) are recorded as minor pests of the developing fruits of coconut. Coccophagus silvestrii Compere (Aphelinidae), Scymnus sp. (Coccinellidae), Pseudoscymnus sp. (Coccinellidae) Telsimia ceylonica (Weise) (Coccinellidae), Cryptogonus bryanti Kapur (Coccinellidae) and Cybocephalus sp. (Nitidulidae) are recorded as their parasitoids and predators. These natural enemies are probably responsible for the control of these pests in the field. -
Evaluating the Effect of Some Botanical Insecticides on the Citrus Mealybug Planococcus Citri (Risso) (Hemiptera: Pseudococcidae)
African Journal of Biotechnology Vol. 11(53), pp. 11620-11624, 3 July, 2012 Available online at http://www.academicjournals.org/AJB DOI:10.5897//AJB11.4226 ISSN 1684-5315 ©2012 Academic Journals Full Length Research Paper Evaluating the effect of some botanical insecticides on the citrus mealybug Planococcus citri (Risso) (Hemiptera: Pseudococcidae) Ahmadi, M.1, Amiri-Besheli, B.1* and Hosieni, S. Z.2 1Department of Agricultural Entomology Sari Agricultural University, Sari, Iran. 2Plant Breeding Sari Agricultural University, Sari, Iran. Accepted 23 May, 2012 Planococcus citri (Risso) (Homoptera: Pseudococcidae), is one of the key pests of citrus. The use of chemical pesticides for a long time can cause many problems such as pesticide resistance, as well as having an adverse effect on the environment. The use of chemical pesticides needs to be replaced with non-chemical control methods. The effects of tondexir (pepper extract) and palizin (eucalyptus extract) using five doses (500, 1000, 1500, 2000 and 3000 ppm) and sirinol (garlic extract) with five doses (1000, 1500, 2000, 2500 and 3500 ppm) on citrus mealybug was investigated. The effect of barter (a botanical synergist) using a single dose (1000 ppm) being added to tondexir and palizin at three doses (500, 1000 and 1500 ppm) and barter (1000 ppm) added to sirinol at four doses (1000, 1500, 2000 and 2500) on citrus mealybug was examined. Mortality was recorded after 24, 48, 72 and 96 h post-treatments. Analysis of variance showed that the highest mortality with 3000 ppm doses of tondexir and palizin was 90/60 ± 2/93 and 89/16 ± 1/92% with sirinol (3500 ppm) with 87.11 ± 1.11% mortality, respectively. -
The Green Lacewings of the Genus Chrysopa in Maryland ( Neuroptera: Chrysopidae)
The Green Lacewings of the Genus Chrysopa in Maryland ( Neuroptera: Chrysopidae) Ralph A. Bram and William E. Bickley Department of Entomology INTRODUCTION Tlw green lacewings which are members of the genus Chrysopa are extreme- ly lwndicia1 insects. The larvae are commonly called aphislions and are well known as predators of aphids and other injurious insects. They play an important part in the regulation of populations of pests under natural conditions, and in California they have been cultured in mass and released for the control of mealy- bugs ( Finney, 1948 and 1950) . The positive identification of members of the genus is desirable for the use of biological-control workers and entomologists in general. Descriptions of most of the Nearctic species of Chrysopidae have relied heavily on body pigmentation and to a lesser extent on wing shape, venational patterns and coloration. Specimens fade when preserved in alcohol or on pins, and natural variation in color patterns occurs in many species ( Smith 1922, Bickley 1952). It is partly for these reasons that some of the most common and relatively abundant representatives of the family are not easily recognized. The chrysopid fauna of North America was treated comprehensively by Banks ( 1903). Smith ( 1922) contributed valuable information about the biology of the green lacewings and about the morphology and taxonomy of the larvae. He also pro- vided k<'ys and other help for the identification of species from Kansas ( 1925, 1934) and Canada ( 1932). Froeschner ( 194 7) similarly dealt with Missouri species. Bickley and MacLeod ( 1956) presented a review of the family as known to occur in the N earctic region north of Mexico. -
Feeding Potential of Cryptolaemus Montrouzieri Against the Mealybug Phenacoccus Solenopsis
Phytoparasitica DOI 10.1007/s12600-011-0211-3 Feeding potential of Cryptolaemus montrouzieri against the mealybug Phenacoccus solenopsis Harmeet Kaur & J. S. Virk Received: 25 August 2011 /Accepted: 1 December 2011 # Springer Science+Business Media B.V. 2011 Abstract Phenacoccus solenopsis Tinsley (Hemiptera: Keywords Biocontrol agent . Cotton . Ladybird . Pseudococcidae) is an exotic species native to the USA, North India damaging cotton and other plant families. The feeding potential of different development stages of Cryptolae- mus montrouzieri Mulsant, a biological control agent Introduction against mealybugs, was investigated on different devel- opment stages of P. solenopsis. Fourth instar grubs and Mealybugs are sap-sucking insects that cause severe adults of C. montrouzieri were the most voracious economic damage to a wide range of crops (Nagrare et feeders on different instars of mealybug. The number al. 2009). The cotton mealybug, Phenacoccus sole- of 1st instar nymphs of mealybug consumed by 1st,2nd, nopsis Tinsley (Hemiptera: Pseudococcidae), was 3rd and 4th instar larvae and adult beetles of C. montrou- reported originally on ornamental and fruit crops in zieri was 15.56, 41.01, 125.38, 162.69 and 1613.81, the United States (Tinsley 1898) and regarded as an respectively. The respective numbers of 2nd and 3rd exotic pest in South East Asia, including India and instar nymphs of mealybug consumed were 11.15 and Pakistan. Fuchs et al. (1991) provided the first report 1.80, 26.35 and 6.36, 73.66 and 13.32, 76.04 and 21.16, of P. solenopsis infesting cultivated cotton and 29 787.95 and 114.66. -
Diptera - Cecidomyiidae, Trypetidae, Tachinidae, Agromyziidae
DIPTERA - CECIDOMYIIDAE, TRYPETIDAE, TACHINIDAE, AGROMYZIIDAE. DIPTERA Etymology : Di-two; ptera-wing Common names : True flies, Mosquitoes, Gnats, Midges, Characters They are small to medium sized, soft bodied insects. The body regions are distinct. Head is often hemispherical and attached to the thorax by a slender neck. Mouthparts are of sucking type, but may be modified. All thoracic segments are fused together. The thoracic mass is largely made up of mesothorax. A small lobe of the mesonotum (scutellum) overhangs the base of the abdomen. They have a single pair of wings. Forewings are larger, membranous and used for flight. Hindwings are highly reduced, knobbed at the end and are called halteres. They are rapidly vibrated during flight. They function as organs of equilibrium.Flies are the swiftest among all insects. Metamorphosis is complete. Larvae of more common forms are known as maggots. They are apodous and acephalous. Mouthparts are represented as mouth hooks which are attached to internal sclerites. Pupa is generally with free appendages, often enclosed in the hardened last larval skin called puparium. Pupa belongs to the coarctate type. Classification This order is sub divided in to three suborders. I. NMATOCERA (Thread-horn) Antenna is long and many segmented in adult. Larval head is well developed. Larval mandibles act horizontally. Pupa is weakly obtect. Adult emergence is through a straight split in the thoracic region. II. BRACHYCERA (Short-horn) Antenna is short and few segmented in adult. Larval head is retractile into the thorax Larval mandibles act vertically Pupa is exarate. Adult emergence is through a straight split in the thoracic region. -
Federal Register/Vol. 81, No. 216/Tuesday, November 8, 2016
Federal Register / Vol. 81, No. 216 / Tuesday, November 8, 2016 / Notices 78567 Done in Washington, DC, this 2nd day of forth the permit application On March 16, 2016, APHIS received November 2016. requirements and the notification a permit application from Cornell Kevin Shea, procedures for the importation, University (APHIS Permit Number 16– Administrator, Animal and Plant Health interstate movement, or release into the 076–101r) seeking the permitted field Inspection Service. environment of a regulated article. release of GE DBMs in both open and [FR Doc. 2016–26941 Filed 11–7–16; 8:45 am] Subsequent to a permit application caged releases. We are currently BILLING CODE 3410–34–P from Cornell University (APHIS Permit preparing an EA for this new Number 13–297–102r) seeking the application and will publish notices permitted field release of three strains of associated with the EA and FONSI (if DEPARTMENT OF AGRICULTURE GE diamondback moth (DBM), Plutella one is reached) in the Federal Register. xylostella, strains designated as Animal and Plant Health Inspection Done in Washington, DC, this 2nd day of OX4319L-Pxy, OX4319N-Pxy, and November 2016. Service OX4767A-Pxy, which have been Kevin Shea, genetically engineered to exhibit red [Docket No. APHIS–2014–0056] Administrator, Animal and Plant Health fluorescence (DsRed2) as a marker and Inspection Service. repressible female lethality, on August Withdrawal of an Environmental [FR Doc. 2016–26935 Filed 11–7–16; 8:45 am] Assessment for the Field Release of 28, 2014, the Animal and Plant Health BILLING CODE 3410–34–P Genetically Engineered Diamondback Inspection Service (APHIS) published in Moths the Federal Register a notice 1 (79 FR 51299–51300, Docket No. -
Green Lacewings Family Chrysopidae
Beneficial Insects Class Insecta, Insects Order Neuroptera, Lacewings, mantids and others Neuroptera means “nerve wings” and refers to the hundreds of veins in their wings. The order Neuroptera is comprised of several small families. Larvae and adults are usually predaceous. Some families are uncommon while others are present more in the south and west. All neuropterans have chewing mouthparts. Green lacewings Family Chrysopidae Description and life history: Adults are green, 15–20 mm long, and slender. They have large, clear membranous wings with green veins and margins, which they hold over their body like a roof. Most have long hair-like antennae and golden eyes. Oval, white eggs are laid singly on a stalk approximately 8 mm long. Larvae are small, gray, and slender, and have large sickle-shaped mouthparts with which to puncture prey. When they reach approximately 10 mm, they spin a silken cocoon and pupate on the underside of a leaf. There are one to ten generations per year. Prey species: Green lacewing adults require high-energy foods such as honeydew and pollen. Larvae prey on aphids and other small, soft-bodied insects, and are nicknamed “aphid-lions.” Some adults are also preda- Green lacewing cocoons containing pupa. (357) ceous. Eggs, larvae, and adults are commercially avail- Photo: John Davidson able and may be purchased from insectaries. These common insects feed in fields, orchards, and gardens. They are commercially available. Chrysoperla carnea, green lacewing adult. (356) Photo: David Laughlin Green lacewing eggs on stalks. (359) Photo: John Davidson Green lacewing larva. (358) Photo: John Davidson IPM of Midwest Landscapes 278. -
Biology of Planococcus Citri (Risso) (Hemiptera: Pseudococcidae) on Five Yam Varieties in Storage
Advances in Entomology, 2014, 2, 167-175 Published Online October 2014 in SciRes. http://www.scirp.org/journal/ae http://dx.doi.org/10.4236/ae.2014.24025 Biology of Planococcus citri (Risso) (Hemiptera: Pseudococcidae) on Five Yam Varieties in Storage Emmanuel Asiedu, Jakpasu Victor Kofi Afun, Charles Kwoseh Department of Crop and Soil Sciences, College of Agriculture and Natural Resources, Kwame Nkrumah University of Science and Technology, Kumasi, Ghana Email: [email protected] Received 25 June 2014; revised 30 July 2014; accepted 18 August 2014 Copyright © 2014 by authors and Scientific Research Publishing Inc. This work is licensed under the Creative Commons Attribution International License (CC BY). http://creativecommons.org/licenses/by/4.0/ Abstract Yam is an important staple cash crop, which constitutes 53% of total root and tuber consumption in West Africa. It is a cheap source of carbohydrate in the diets of millions of people worldwide and in tropical West Africa. However, attack by Planococcus citri results in shriveling of the tubers, making them become light and unpalatable. They also lose their market value. The total number of eggs laid, incubation period, developmental period and adult longevity of P. citri on stored yam Disocorea species were studied on five yam varieties namely Dioscorea rotundata var. Pona, Dios- corea rotundata var. Labreko, Dioscorea rotundata var. Muchumudu, Disocorea alata var. Matches and Dioscorea rotundata var. Dente in the laboratory with ambient temperatures of 26.0˚C - 30.0˚C and relative humidity of 70.0% - 75.0%. The mean life spans of the female insect that is from hatch to death on Dioscorea rotundata var. -
UFRJ a Paleoentomofauna Brasileira
Anuário do Instituto de Geociências - UFRJ www.anuario.igeo.ufrj.br A Paleoentomofauna Brasileira: Cenário Atual The Brazilian Fossil Insects: Current Scenario Dionizio Angelo de Moura-Júnior; Sandro Marcelo Scheler & Antonio Carlos Sequeira Fernandes Universidade Federal do Rio de Janeiro, Programa de Pós-Graduação em Geociências: Patrimônio Geopaleontológico, Museu Nacional, Quinta da Boa Vista s/nº, São Cristóvão, 20940-040. Rio de Janeiro, RJ, Brasil. E-mails: [email protected]; [email protected]; [email protected] Recebido em: 24/01/2018 Aprovado em: 08/03/2018 DOI: http://dx.doi.org/10.11137/2018_1_142_166 Resumo O presente trabalho fornece um panorama geral sobre o conhecimento da paleoentomologia brasileira até o presente, abordando insetos do Paleozoico, Mesozoico e Cenozoico, incluindo a atualização das espécies publicadas até o momento após a última grande revisão bibliográica, mencionando ainda as unidades geológicas em que ocorrem e os trabalhos relacionados. Palavras-chave: Paleoentomologia; insetos fósseis; Brasil Abstract This paper provides an overview of the Brazilian palaeoentomology, about insects Paleozoic, Mesozoic and Cenozoic, including the review of the published species at the present. It was analiyzed the geological units of occurrence and the related literature. Keywords: Palaeoentomology; fossil insects; Brazil Anuário do Instituto de Geociências - UFRJ 142 ISSN 0101-9759 e-ISSN 1982-3908 - Vol. 41 - 1 / 2018 p. 142-166 A Paleoentomofauna Brasileira: Cenário Atual Dionizio Angelo de Moura-Júnior; Sandro Marcelo Schefler & Antonio Carlos Sequeira Fernandes 1 Introdução Devoniano Superior (Engel & Grimaldi, 2004). Os insetos são um dos primeiros organismos Algumas ordens como Blattodea, Hemiptera, Odonata, Ephemeroptera e Psocopera surgiram a colonizar os ambientes terrestres e aquáticos no Carbonífero com ocorrências até o recente, continentais (Engel & Grimaldi, 2004). -
The First Green Lacewings from the Late Eocene Baltic Amber
The first green lacewings from the late Eocene Baltic amber VLADIMIR N. MAKARKIN, SONJA WEDMANN, and THOMAS WEITERSCHAN Makarkin, V.N., Wedmann, S., and Weiterschan, T. 2018. The first green lacewings from the late Eocene Baltic amber. Acta Palaeontologica Polonica 63 (3): 527–537. Pseudosencera baltica gen. et sp. nov. of Chrysopinae (Chrysopidae, Neuroptera) is described from Baltic amber. Additionally, another species, Nothochrysa? sp. (Nothochrysinae), is left in the open nomenclature. Pseudosencera bal- tica gen. et sp. nov. represents the oldest confident record of Chrysopinae. The new genus lacks the apparent forewing intramedian cell, and possesses three character states not found in other Chrysopinae: the simple AA1, the short basal crossvein between M and Cu, and 5‒6 rings of setae on the antennal flagellomeres. This genus is probably a special- ised form in a basal branch of Chrysopinae, that could not be attributed to any of the known tribes. The specimen of Nothochrysa? sp. consists only of fragments of the forewings. The late Eocene Baltic amber represents the oldest horizon where Chrysopinae and Nothochrysinae are found to coexist. It is highly likely that Chrysopidae were extremely rare in these forests. Key words: Neuroptera, Chrysopinae, Nothochrysinae, Cenozoic, Baltic amber. Vladimir N. Makarkin [[email protected]], Federal Scientific Center of the East Asia Terrestrial Biodiversity, Far Eastern Branch of the Russian Academy of Sciences, Vladivostok 690022, Russia. Sonja Wedmann [[email protected]], Senckenberg Forschungsstation Grube Messel, Markstrasse 35, D-64409 Messel, Germany. Thomas Weiterschan [[email protected]], Forsteler Strasse 1, 64739 Höchst Odw., Germany. Received 16 May 2018, accepted 5 July 2018, available online 23 July 2018. -
Jumping Mechanisms in Lacewings (Neuroptera, Chrysopidae And
© 2014. Published by The Company of Biologists Ltd | The Journal of Experimental Biology (2014) 217, 4252-4261 doi:10.1242/jeb.110841 RESEARCH ARTICLE Jumping mechanisms in lacewings (Neuroptera, Chrysopidae and Hemerobiidae) Malcolm Burrows1,* and Marina Dorosenko1 ABSTRACT increases the complexity of muscle control but has the advantage of Lacewings launch themselves into the air by simultaneous propulsive increasing the muscle mass that can be devoted to jumping while movements of the middle and hind legs as revealed in video images avoiding the specialisation in shape and size of the legs. In snow captured at a rate of 1000 s−1. These movements were powered fleas it also allows four energy stores – one for each leg – to be used largely by thoracic trochanteral depressor muscles but did not start in its catapult jumping action (Burrows, 2011). Furthermore, by from a particular preset position of these legs. Ridges on the lateral distributing ground reaction forces over a larger surface area, take- sides of the meso- and metathorax fluoresced bright blue when off becomes possible from more compliant surfaces. For the fly illuminated with ultraviolet light, suggesting the presence of the elastic Hydrophorus alboflorens this even enables jumping from the surface protein resilin. The middle and hind legs were longer than the front of water by ensuring that the legs do not penetrate the surface legs but their femora and tibiae were narrow tubes of similar (Burrows, 2013a). diameter. Jumps were of two types. First, those in which the body In all jumping movements, the same demands exist for high take- was oriented almost parallel to the ground (−7±8 deg in green off velocities and short acceleration times, particularly when escape lacewings, 13.7±7 deg in brown lacewings) at take-off and remained is the required outcome. -
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Vol. 14(1), pp. 18-23, 3 January, 2019 DOI: 10.5897/AJAR2018.13631 Article Number: 1C2697159695 ISSN: 1991-637X Copyright ©2019 African Journal of Agricultural Author(s) retain the copyright of this article http://www.academicjournals.org/AJAR Research Full Length Research Paper Natural occurrence of Diadiplosis megalamellae (Barnes) in mealybugs on roses in Kenya Anouk H. J. Hoogendoorn, Ruth Murunde*, Evans Otieno and Henry Wainwright The Real IPM Company (K) Ltd, P. O. Box 4001-01002, Madaraka, Thika, Kenya. Received 15 October, 2018; Accepted 27 November, 2018 Over the last decade there has been an increasing adoption of Integrated Pest Management on rose farms in Kenya. As a consequence, there has been a rise in secondary pests on rose plants, including in particular the citrus mealybug Planococcus citri (Risso). On cut flowerrose farms in Kenya, the presence of the predatory midge Diadiplosis megalamellae (Barnes) (Diptera: Cecidomyiidae) was observed. Therefore, a survey was carried out to quantify the occurrence of D. megalamellae and the association with mealybug infestations in commercial cut flower rose crops in Kenya. Four farms in four different regions of Kenya and eight rose varieties were surveyed. The midge D. megalamellae was present on farms located in Naivasha, Nairobi and Thika, but was absent in Nanyuki region. The midge D. megalamellae was found mainly in P. citri mealybug colonies and, although in much lower numbers, in the long tailed mealybug Pseudococcus longispinus (Targioni Tozzetti) colonies. The number of mealybugs was positively correlated with the number of number of D. megalamellae larvae suggesting increased multiplication of the D.