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New Records of the Family Chalcididae (Hymenoptera: Chalcidoidea) from Egypt
Zootaxa 4410 (1): 136–146 ISSN 1175-5326 (print edition) http://www.mapress.com/j/zt/ Article ZOOTAXA Copyright © 2018 Magnolia Press ISSN 1175-5334 (online edition) https://doi.org/10.11646/zootaxa.4410.1.7 http://zoobank.org/urn:lsid:zoobank.org:pub:6431DC44-3F90-413E-976F-4B00CFA6CD2B New records of the family Chalcididae (Hymenoptera: Chalcidoidea) from Egypt MEDHAT I. ABUL-SOOD1 & NEVEEN S. GADALLAH2,3 1Zoology Department, Faculty of Science (Boys), Al-Azhar University, P.O. Box 11884, Nasr City, Cairo, Egypt. E-mail: [email protected] 2Entomology Department, Faculty of Science, Cairo University, Giza, Egypt 3Corresponding author. E-mail: [email protected] Abstract In the present study, a checklist of new records of the family Chalcididae of Egypt is presented based on a total of 180 specimens collected from 24 different Egyptian localities between June 2011 and October 2016, mostly by sweeping and Malaise traps. Nineteen species as well as the subfamily Epitraninae and the genera Bucekia Steffan, Epitranus Walker, Proconura Dodd, and Tanycoryphus Cameron, are newly recorded from Egypt. A single species previously placed in the genus Hockeria is transferred to Euchalcis Dufour as E. rufula (Nikol’skaya, 1960) comb. nov. Key words: Parasitic wasps, Chalcidinae, Dirhininae, Epitraninae, Haltichellinae, new records, new combination Introduction The Chalcididae (Hymenoptera: Chalcidoidea) is a medium-sized family represented by more than 1500 described species in 93 genera (Aguiar et al. 2013; Noyes 2017; Abul-Sood et al. 2018). A large number of described species are classified in the genus Brachymeria Westwood (about 21%), followed by Conura Spinola (20.3%) (Noyes 2017). -
Hymenoptera: Chalcididae) in the European Continent
Travaux du Muséum National d’Histoire Naturelle “Grigore Antipa” 64 (1): 61–65 (2021) doi: 10.3897/travaux.64.e66165 FAUNISTIC NOTE First record of the subfamily Epitraninae (Hymenoptera: Chalcididae) in the European Continent Evangelos Koutsoukos1, 2, Gerard Delvare3 1 Section of Ecology and Systematics, Department of Biology, National and Kapodistrian University of Athens, 15784 Athens, Greece 2 Museum of Zoology, National and Kapodistrian University of Athens, 15784 Athens, Greece 3 Centre de Coopération Internationale en Recherche Agronomique pour le Développement (CIRAD), Montpellier SupAgro, INRA, IRD, Univ. Montpellier, Montpellier, France Corresponding author: Evangelos Koutsoukos ([email protected]) Received 19 March 2021 | Accepted 25 May 2021 | Published 30 June 2021 Citation: Koutsoukos E, Delvare G (2021) First record of the subfamily Epitraninae (Hymenoptera: Chalcididae) in the European Continent. Travaux du Muséum National d’Histoire Naturelle “Grigore Antipa” 64(1): 61–65. https:// doi.org/10.3897/travaux.64.e66165 Abstract Epitraninae Burks (Hymenoptera: Chalcididae) is a subfamily with a single recognised genus, Epitranus Walker, known to be distributed throughout the tropical areas of the Old World. Whilst recent studies have reported the presence of Epitraninae in countries of the Middle East, there are no published records from the European continent. A female specimen belonging to the Epitranus hamoni species complex was collected in Salamis island, Attica, Greece, and deposited at the Museum of Zoology (Athens). This record constitutes an important addition to the Greek and European Chalcidoidea fauna. Keywords Chalcidoidea, Chalcididae, new record, Epitranus, Greece. Introduction Chalcidid wasps (Chalcidoidea: Chalcididae) are a moderate sized family regarding species number (Aguiar et al. -
A Phylogenetic Analysis of the Megadiverse Chalcidoidea (Hymenoptera)
UC Riverside UC Riverside Previously Published Works Title A phylogenetic analysis of the megadiverse Chalcidoidea (Hymenoptera) Permalink https://escholarship.org/uc/item/3h73n0f9 Journal Cladistics, 29(5) ISSN 07483007 Authors Heraty, John M Burks, Roger A Cruaud, Astrid et al. Publication Date 2013-10-01 DOI 10.1111/cla.12006 Peer reviewed eScholarship.org Powered by the California Digital Library University of California Cladistics Cladistics 29 (2013) 466–542 10.1111/cla.12006 A phylogenetic analysis of the megadiverse Chalcidoidea (Hymenoptera) John M. Heratya,*, Roger A. Burksa,b, Astrid Cruauda,c, Gary A. P. Gibsond, Johan Liljeblada,e, James Munroa,f, Jean-Yves Rasplusc, Gerard Delvareg, Peter Jansˇtah, Alex Gumovskyi, John Huberj, James B. Woolleyk, Lars Krogmannl, Steve Heydonm, Andrew Polaszekn, Stefan Schmidto, D. Chris Darlingp,q, Michael W. Gatesr, Jason Motterna, Elizabeth Murraya, Ana Dal Molink, Serguei Triapitsyna, Hannes Baurs, John D. Pintoa,t, Simon van Noortu,v, Jeremiah Georgea and Matthew Yoderw aDepartment of Entomology, University of California, Riverside, CA, 92521, USA; bDepartment of Evolution, Ecology and Organismal Biology, Ohio State University, Columbus, OH, 43210, USA; cINRA, UMR 1062 CBGP CS30016, F-34988, Montferrier-sur-Lez, France; dAgriculture and Agri-Food Canada, 960 Carling Avenue, Ottawa, ON, K1A 0C6, Canada; eSwedish Species Information Centre, Swedish University of Agricultural Sciences, PO Box 7007, SE-750 07, Uppsala, Sweden; fInstitute for Genome Sciences, School of Medicine, University -
False Codling Moth Thaumatotibia Leucotreta
Stone Fruit Commodity-Based Pest Survey False Codling Moth Thaumatotibia leucotreta Introduction False codling moth (Figure 1) is a significant pest because of its potential economic impact on many crops, including stone fruit, avocado, citrus, corn, cotton, and macadamia. It is not currently known to be present in the United States. Biology Depending on conditions, the false codling moth’s life cycle ranges from 30 to 174 days. It can produce from 2 to 10 generations each year, depending on multiple factors including temperature, food availability and quality, and humidity. To attract males, adult females release pheromones at FIGURE 1. Adult false codling moth (Thaumatotibia leucotreta). Photo courtesy of night. After the adults mate, the female deposits eggs on Pest and Diseases Image Library, Bugwood.org. host plants, either in batches or as single eggs. Later, the hatching larvae burrow into the rind of the host plant. Mature larvae spin cocoons and pupate before they emerge as adults. Symptoms False codling moth can attack stone fruit at any stage. Larvae can even develop in hard green fruit prior to application of control measures. Larvae burrow at the stem end into the fruit and cause damage by feeding around the stone. Damaged fruit can become vulnerable to secondary pests such as fungal organisms and scavengers. Peaches can be damaged by larvae beginning up to 6 weeks before harvest. False codling moth can also attack plants unsuitable for larvae development, such as avocado, causing lesions on fruit tissue and diminishing the marketability of fruit. Because false codling moth is an internal feeder, few symptoms are actually displayed by the larvae. -
(Diptera: Tephritidae) Control in Mango
OPTIMIZATION OF AN INTEGRATED PEST MANAGEMENT PROGRAM FOR FRUIT FLIES (DIPTERA: TEPHRITIDAE) CONTROL IN MANGO: A CASE OF MANICA PROVINCE, MOZAMBIQUE LAURA DA GRAҪA JOSÉ CANHANGA A THESIS SUBMITTED IN FULFILMENT OF THE REQUIREMENTS FOR THE DEGREE OF DOCTOR OF PHILOSOPHY OF SOKOINE UNIVERSITY OF AGRICULTURE. MOROGORO, TANZANIA. 2018 ii EXTENDED ABSTRACT This study was undertaken to reduce the losses caused by Bactrocera dorsalis (Hendel) in Manica province, Mozambique, through an optimized integrated pest management (IPM) package. It involved interviews with farmers to collect baseline information on awareness of fruit producers regarding fruit fly pests and their management so that an IPM package can be developed based on the farmers’ needs. Additionally, systematic trapping data of B. dorsalis seasonality and damage were collected and economic injury level (EIL) for B. dorsalis was estimated. Based on EIL, the IPM for B. dorsalis control developed in Tanzania by the Sokoine University of Agriculture (SUA IPM) was optimized. The SUA IPM included calendar GF 120 NF bait sprays and orchard sanitation while for the optimized IPM the GF 120 NF was only sprayed in the subplots inside the orchard when the threshold of 30 flies/trap/week was reached. The effectiveness of SUA IPM and its optimized version were also tested. Results showed that fruit flies were the main pest problem in mango and citrus orchards. More than 70% the respondents indicated low fruit quality and increasing volumes of uncommercial zed fruits as consequences of fruit flies infestation. The monetary value of losses reached a value of USD 135,784.8 during 2014/15 mango season. -
Biological Responses and Control of California Red Scale Aonidiella Aurantii (Maskell) (Hemiptera: Diaspididae)
Biological responses and control of California red scale Aonidiella aurantii (Maskell) (Hemiptera: Diaspididae) by Khalid Omairy Mohammed Submitted to Murdoch University in fulfilment of the requirements for the degree of Doctor of Philosophy College of Science, Health, Engineering and Education Murdoch University Perth, Western Australia March 2020 Declaration The work described in this thesis was undertaken while I was an enrolled student for the degree of Doctor of Philosophy at Murdoch University, Western Australia. I declare that this thesis is my own account of my research and contains as its main content work which has not previously been submitted for a degree at any tertiary education institution. To the best of my knowledge, all work performed by others, published or unpublished, has been duly acknowledged. Khalid O. Mohammed Date: March 10, 2020 I Acknowledgements بِ ْس ِمِِاللَّ ِـه َِّالر ْح َم ٰـ ِن َِّالر ِح ِيمِ ُ َويَ ْسأَلُ َونَك َِع ِن ُِّالروحِِِۖقُ ِل ُِّالر ُوح ِِم ْنِأَ ْم ِر َِر ِب َيِو َماِأ ِوتيتُ ْم ِِم َن ِْال ِع ْل ِمِإِ ََّّل َِق ِل ايًلِ﴿٨٥﴾ The research for this thesis was undertaken in the School of Veterinary and Life Science, Murdoch University. I would like to express my heartfelt gratitude to my supervisors Professor Yonglin Ren and Dr Manjree Agarwal “Postharvest Biosecurity and Food Safety Laboratory Murdoch” for their support with enthusiasm, constructive editing, and patience throughout the years of this wonderful project. I deeply appreciate their encouragement, assistance and for being so willing to take me on as a student. I would like to express my sincere gratitude to all those who helped me in completing this thesis. -
False Codling Moth on Chillies Thaumatotibia Leucotreta Prevention Monitoring Direct Control
PEST MANAGEMENT DECISION GUIDE: GREEN LIST False codling moth on chillies Thaumatotibia leucotreta Prevention Monitoring Direct Control l Use mesh or net barriers to keep the l Start monitoring when the chilli fruits start developing as the larvae only attack l Control is difficult because the moth pest out of the crop when possible the fruits has many alternative hosts so l Insect: reinfestation is likely to occur l Eggs are less than 1 mm long, oval, flattened and difficult to see. They are l Hand pick the mature larvae from the laid singly or in group on the developing fruits crop Larva T. leucotreta (Tertia l Larvae are yellowish-white when young with dark spots. The full grown larva l If available, spray a mating disruption Grové, Institute for Tropical and is about 15 mm long, bright red or pink, with a yellow-brown head. The young pheromone into the crop to stop the Subtropical Crops, larvae mine fruit just beneath the surface, or bore into the skin causing males and females from mating Bugwood.org) premature ripening of the fruit l Destroy fruits that are infested and l The pupa (5-7 mm long) is contained within a tough silken cocoon and can be have fallen to the ground to reduce seen in the soil or amongst plant debris the build-up cycle and avoid carrying over the pest to the next season. Put l Adult moths are 15-16 mm (males) and 19-20 mm (female) in length. the fruits in plastic bags and expose Forewings have grey, brown, black and orange-brown markings. -
Thaumatotibia Leucotreta
Thaumatotibia leucotreta Scientific Name Thaumatotibia leucotreta (Meyrick) Synonyms: Cryptophlebia leucotreta (Meyrick), Cryptophlebia roerigii Zacher Olethreutes leucotreta Meyrick Thaumatotibia roerigii Zacher Common Name(s) False codling moth, citrus codling moth, orange moth, and orange codling moth Type of Pest Moth Figure 1. Larva of Thaumatotibia leucotreta (T. Grove Taxonomic Position and W. Styn, bugwood.org). Class: Insecta, Order: Lepidoptera, Family: Tortricidae Reason for Inclusion CAPS Target: AHP Prioritized Pest List - 2003 through 2014 Pest Description Eggs: Eggs are flat, oval (0.77 mm long by 0.60 mm wide) shaped discs with a granulated surface. The eggs are white to cream colored when initially laid. They change to a reddish color before the black head capsule of the larvae becomes visible under the chorion prior to hatching (Daiber, 1979a). 1 Larvae: First instar (neonate) larvae approximately 1 to 1.2 mm (< /16 in) in length with dark pinacula giving a spotted appearance, fifth instar larvae are orangey-pink, 1 becoming more pale on sides and yellow in ventral region, 12 to 18 mm (approx. /2 to 11 /16 in) long, with a brown head capsule and prothoracic shield (Fig. 1). [Note this coloration is only present in live specimens.] The last abdominal segment bears an anal comb with two to ten “teeth.” The mean head capsule width for the first through fifth instar larvae has been recorded as: 0.22, 0.37, 0.61, 0.94 and 1.37 mm, respectively (Daiber, 1979b). Diagnostic characters would include the anal comb with two to ten teeth in addition to: L pinaculum on T1 enlarged and extending beneath and beyond (posterad of) the spiracle; spiracle on A8 displaced posterad of SD pinaculum; crochets unevenly triordinal, 36-42; L-group on A9 usually trisetose (all setae usually on same pinaulum) (Brown, 2011). -
False Codling Moth
Fact sheet False codling moth What is the False codling moth? The False codling moth (Cryptophlebia leucotreta) is an internal fruit feeding moth that can be found throughout the year in warm climates and has been recorded as feeding on over 50 different plant species. This moth causes economic loss in a range of crops in sub-Saharan Africa. Losses during infestations can be between 20-30%. What does it look like? Adult moths are 15-16 mm (males) and 19-20 mm Citrus Research International, Bugwood.org J.H. Hofmeyr, (female) in length. Forewings have grey, brown, Eggs are oval shaped and almost 1 mm long black and orange-brown markings. A triangular marking on the outer part of the wing with a crescent shaped marking above it distinguishes the False codling moth from other species. Young larvae are yellowish-white with dark spots but bright red or pink when fully grown (15 mm), with a yellow-brown head. Pupae are contained within a tough silken cocoon amongst debris or in the soil. Female moths lay 100-400 eggs (oval, flattened and almost 1 mm in length) singly on the fruits at night. J.H. Hofmeyr, Citrus Research International, Bugwood.org J.H. Hofmeyr, What can it be confused with? False codling moth pupae False codling moth can look similar to other moths but can be distinguished by the triangular marking near the edges of the wings. What should I look for? The young larvae mine fruit just beneath the surface, or bore into the skin causing premature ripening of the fruit. -
Appendix S4. the Tentorium and Its External Landmarks in the Chalcididae
Appendix S4 . The tentorium and its external landmarks in the Chalcididae This study is the first in the whole superfamily Chalcidoidea to investigate the tentorium as a phylogenetic character and to establish the connection between the inner skeleton of the cephalic capsule and its external landmarks on the back of the head. In this section, details are provided on the methodology used by GD to examine and code the different bridges. S4.1. Context Phylogenetic informativeness of the characters of the head capsule in Hymenoptera was recently highlighted (Vilhelmsen 2011; Burks & Heraty 2015; Zimmermann & Vilhelmsen 2016). However, interpretation is difficult and requires landmarks (Burks & Heraty, 2015). More precisely, the identity of the sclerotized structures between the occipital foramen and the oral fossa are still debated. Homology and nomenclature of these structures were established by Snodgrass (1928, 1942 and 1960) and reassessed by Vilhelmsen (1999) and Burks & Heraty (2015). These authors describe various types of ‘bridges’, such as postgenal, hypostomal and subforaminal bridges, according to the cephalic part – postgena or hypostoma – from which they putatively originate. In his phylogenetic analyses of the Chalcididae, Wijesekara (1997a & 1997b) used the back of the head – reduced to a single character – and distinguished an ‘hypostomal bridge’ and a ‘genal bridge’. The detailed examination of the back of the head in the Eurytomidae (Lotfalizadeh et al. 2007), probable sister group of the Chalcididae, provided useful characters for their phylogeny and prompted GD to also investigate these characters in the Chalcididae. Chalcididae exhibit variable and puzzling structures that may be phylogenetically informative but request a thorough identification of homologies among the subfamilies and more largely with other families of Chalcidoidea. -
New Pest Response Guidelines False Codling Moth Thaumatotibia Leucotreta
United States Department of New Pest Response Agriculture Marketing and Regulatory Guidelines Programs Animal and False Codling Moth Plant Health Inspection Service Thaumatotibia leucotreta Cooperating State Departments of Agriculture August 13, 2007 New Pest Response Guidelines False Codling Moth Thaumatotibia leucotreta August 13, 2007 New Pest Response Guidelines: False Codling Moth Thaumatotibia leucotreta was prepared by Jeffrey Stibick, USDA–APHIS–PPQ–Emergency and Domestic Programs and edited by Patricia S. Michalak, USDA–APHIS–PPQ–Manuals Unit. Cite this report as follows: Stibick, J. 2006. New Pest Response Guidelines: False Codling Moth Thaumatotibia leucotreta. USDA–APHIS–PPQ–Emergency and Domestic Programs, Riverdale, Maryland [http://www.aphis.usda.gov/ import_export/plants/ppq_manuals.shtml]. R. L. Dunkle May 3, 2007 Richard Dunkle, Deputy Administrator Date USDA–APHIS–PPQ Emergency and Domestic Programs Emergency Planning Joel Floyd, Team Leader 4700 River Road Unit 137 Riverdale, Maryland 20737 Telephone: 310/734-4396 [email protected] 1 Credits False Codling Moth Contributors Stephanie Bloem, U. S. Department of Agriculture (USDA)–Animal and Plant Health Inspection Service (APHIS)–Center for Plant Health Science and Technology (CPHST), Raleigh, North Carolina Jim E. Carpenter, USDA–Agricultural Research Service (ARS)–Crop Protection and Management Research, Tifton, Georgia Susan Ellis, USDA–APHIS–Plant Protection and Quarantine–Office of the Deputy Administrator, Riverdale, Maryland Todd Gilligan, Ohio State University, Museum of Biodiversity, Columbus, Ohio Jeffrey N. L. Stibick, USDA–APHIS–PPQ–Emergency and Domestic Programs, Riverdale, Maryland Shaharra J. Usnick, USDA–APHIS–PPQ–Plant Health Programs, Riverdale, Maryland Robert C. Venette, USDA–Forest Service, St. Paul, Minnesota Industry, State Regulatory Officers, Universities, and Governmental Agencies as credited in: September 1983. -
False Codling Moth, Thaumatotibia (=Cryptophlebia) Leucotreta (Meyrick) [Lepidoptera: Tortricidae]
Mini Risk Assessment False codling moth, Thaumatotibia (=Cryptophlebia) leucotreta (Meyrick) [Lepidoptera: Tortricidae] Robert C. Venette, Erica E. Davis, Michelle DaCosta, Holly Heisler, & Margaret Larson Department of Entomology, University of Minnesota St. Paul, MN 55108 September 21, 2003 Introduction Thaumatotibia leucotreta is a significant pest of fruit trees and field crops in portions of Africa (CIE 1976, Zhang 1994). Until recently, this pest had been most commonly known as Cryptophlebia leucotreta (Komai 1999). A detailed description of the rationale for the name change is included in this document. For the sake of scientific accuracy, we refer to the false codling moth as T. leucotreta throughout this report. We hope the change does not cause confusion. To our knowledge the risks posed by this pest for US agriculture and native ecosystems have not been evaluated previously in a formal pest risk assessment. Figure 1. Larva and adult of T. leucotreta. Images not to scale. [Larval image from http://www.arc.agric.za/institutes/ itsc/main/avocado/moth.htm; Adult image from Georg Goergen/IITA Insect Museum, Cotonou, Benin as published in (CAB 2000)] 1. Ecological Suitability. Rating: Medium. Thaumatotibia leucotreta is native to the Ethiopian zoogeographic province and presently occurs in much of Sub- Saharan Africa (CIE 1976, CAB 2000). Climates in the area occupied by this pest can be characterized as tropical, dry or temperate (CAB 2000). The currently reported global distribution of T. leucotreta suggests that the pest may be most closely associated with biomes that are generally classified as desert and xeric shrubland, tropical and subtropical grasslands, savannas, and shrubland; and tropical and subtropical moist broadleaf forest.