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Journal articles on the topic 'Tephritid fly'

Author: Grafiati

Published: 4 June 2021

Last updated: 10 February 2022

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1

Scolari, Francesca, Federica Valerio, Giovanni Benelli, Nikos T. Papadopoulos, and Lucie Vaníčková. "Tephritid Fruit Fly Semiochemicals: Current Knowledge and Future Perspectives." Insects 12, no. 5 (2021): 408. http://dx.doi.org/10.3390/insects12050408.

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The Dipteran family Tephritidae (true fruit flies) comprises more than 5000 species classified in 500 genera distributed worldwide. Tephritidae include devastating agricultural pests and highly invasive species whose spread is currently facilitated by globalization, international trade and human mobility. The ability to identify and exploit a wide range of host plants for oviposition, as well as effective and diversified reproductive strategies, are among the key features supporting tephritid biological success. Intraspecific communication involves the exchange of a complex set of sensory cues

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2

Zida, Issaka, Souleymane Nacro, Rémy Dabiré, and Irénée Somda. "Seasonal Abundance and Diversity of Fruit Flies (Diptera: Tephritidae) in Three Types of Plant Formations in Western Burkina Faso, West Africa." Annals of the Entomological Society of America 113, no. 5 (2020): 343–54. http://dx.doi.org/10.1093/aesa/saaa004.

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Abstract Fruit flies are significant insect pests, worldwide. Tephritid species diversity and their seasonal abundance were investigated over 2 yr (May 2017 to May 2019) in Western Burkina Faso. A mass trapping experiment consisting of 288 Tephri Trap types, operating with four types of parapheromones comprising methyl eugenol, terpinyl acetate, trimedlure, and cue lure and an insecticide (Dichlorvos), was used for attracting and killing insects. Plant formations including natural fallows, mango orchards, and agroforestry parks in each of the six study sites were selected for data collection.

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3

Biasazin, Tibebe, Haimanot Chernet, Sebastian Herrera, et al. "Detection of Volatile Constituents from Food Lures by Tephritid Fruit Flies." Insects 9, no. 3 (2018): 119. http://dx.doi.org/10.3390/insects9030119.

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Tephritid fruit flies require protein for sexual and gonotrophic development. Food-based lures are therefore widely used in strategies to detect and control fruit flies in the Tephritidae family. However, these baits are attractive to a broad range of insect species. We therefore sought to identify volatiles detected by the fly antennae, with the goal to compose lures that more specifically target tephritids. Using gas chromatography-coupled electroantennographic detection (GC-EAD) we screened for antennal responses of four important tephritid species to volatile compounds from five commercial

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4

Liu, Dengfeng, Yuran Dong, Xinqiang Xi, and Shucun Sun. "The complete mitochondrial genome of the Tephritid fly Tephritis femoralis (Diptera: Tephritidae)." Mitochondrial DNA Part B 5, no. 2 (2020): 1813–14. http://dx.doi.org/10.1080/23802359.2020.1749161.

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5

Mcquate, Grant T., Peter A. Follett, Nicanor J. Liquido, and Charmaine D. Sylva. "Assessment of Navel Oranges, Clementine Tangerines, and Rutaceous Fruits as Hosts of Bactrocera cucurbitae and Bactrocera latifrons (Diptera: Tephritidae)." International Journal of Insect Science 7 (January 2015): IJIS.S20069. http://dx.doi.org/10.4137/ijis.s20069.

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Export of Citrus spp. fruits may require risk mitigation measures if grown in areas with established tephritid fruit fly (Diptera: Tephritidae) populations capable of infesting the fruits. The host status of Citrus spp. fruits is unclear for two tephritid fruit fly species whose geographic ranges have expanded in recent years: melon fly, Bactrocera cucurbitae (Cocquillett), and Bactrocera latifrons (Hendel). In no choice cage infestation studies, B. latifrons oviposited into intact and punctured Washington navel oranges ( Citrus sinensis [L.] Osbeck) and Clementine tangerines ( C. reticulata L

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6

Raza, Muhammad Fahim, Zhichao Yao, Shuai Bai, Zhaohui Cai, and Hongyu Zhang. "Tephritidae fruit fly gut microbiome diversity, function and potential for applications." Bulletin of Entomological Research 110, no. 4 (2020): 423–37. http://dx.doi.org/10.1017/s0007485319000853.

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AbstractThe family Tephritidae (order: Diptera), commonly known as fruit flies, comprises a widely distributed group of agricultural pests. The tephritid pests infest multiple species of fruits and vegetables, resulting in huge crop losses. Here, we summarize the composition and diversity of tephritid gut-associated bacteria communities and host intrinsic and environmental factors that influence the microbiome structures. Diverse members of Enterobacteriaceae, most commonly Klebsiella and Enterobacter bacteria, are prevalent in fruit flies guts. Roles played by gut bacteria in host nutrition,

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7

McQuate, Grant T., Charmaine D. Sylva, and Nicanor J. Liquido. "Natural Field Infestation of Mangifera casturi and Mangifera lalijiwa by Oriental Fruit Fly, Bactrocera dorsalis (Diptera: Tephritidae)." International Journal of Insect Science 9 (January 1, 2017): 117954331771773. http://dx.doi.org/10.1177/1179543317717735.

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Mango, Mangifera indica (Anacardiaceae), is a crop cultivated pantropically. There are, however, many other Mangifera spp (“mango relatives”) which have much more restricted distributions and are poorly known but have potential to produce mango-like fruits in areas where mangoes do not grow well or could be tapped in mango breeding programs. Because of the restricted distribution of many of the Mangifera spp, there has also been limited data collected on susceptibility of their fruits to infestation by tephritid fruit flies which is important to know for concerns both for quality of production

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8

Estes, Anne M., David J. Hearn, Judith L. Bronstein, and Elizabeth A. Pierson. "The Olive Fly Endosymbiont, “Candidatus Erwinia dacicola,” Switches from an Intracellular Existence to an Extracellular Existence during Host Insect Development." Applied and Environmental Microbiology 75, no. 22 (2009): 7097–106. http://dx.doi.org/10.1128/aem.00778-09.

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ABSTRACT As polyphagous, holometabolous insects, tephritid fruit flies (Diptera: Tephritidae) provide a unique habitat for endosymbiotic bacteria, especially those microbes associated with the digestive system. Here we examine the endosymbiont of the olive fly [Bactrocera oleae (Rossi) (Diptera: Tephritidae)], a tephritid of great economic importance. “Candidatus Erwinia dacicola” was found in the digestive systems of all life stages of wild olive flies from the southwestern United States. PCR and microscopy demonstrated that “Ca. Erwinia dacicola” resided intracellularly in the gastric ceca o

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9

Layodé, Babatoundé Ferdinand Rodolphe, Alexis Onzo, and Miriam Frida Karlsson. "Watermelon-infesting Tephritidae fruit fly guild and parasitism by Psyttalia phaeostigma (Hymenoptera: Braconidae)." International Journal of Tropical Insect Science 40, no. 1 (2019): 157–66. http://dx.doi.org/10.1007/s42690-019-00066-x.

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AbstractAn ecological guild of Tephritidae fruit flies exploits cucurbit vegetable fruits, tremendously reducing their production worldwide. Knowledge of the composition of the guild of infesting flies in the field and information on their natural enemy species, might improve pest management strategies. Our aim was therefore to identify Tephritidae species infesting the watermelon Citrullus lanatus (Thunb.) Matsum. & Nakai in the Republic of Benin. Morphological and molecular identification of parasitoid species present in the field collections was also done. Infested watermelons were samp

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10

Jeltsch, F., Ch Wissel, S. Eber, and R. Brandl. "Oscillating dispersal patterns of tephritid fly populations." Ecological Modelling 60, no. 1 (1992): 63–75. http://dx.doi.org/10.1016/0304-3800(92)90013-5.

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11

Shcherbakov, Mikhail V. "A review of leaf-miner tephritid flies (Diptera, Tephritidae) of the south-eastern part of West Siberia, Russia." Acta Biologica Sibirica 6 (December 17, 2020): 637–47. http://dx.doi.org/10.3897/abs.6.e59735.

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Eleven leaf-miner tephritid fly species from 7 genera are reviewed for four regions in the south-eastern part of West Siberia, Russia, namely Tomskaya and Kemerovskaya Oblasts, Altaiskii Krai, and Republics of Altai and Khakassia. The share of leaf-miner species in the tephritid fly fauna of the region is 10.2%. Cornutrypeta svetlanae Richter &amp; Shcherbakov, 2000, recorded from four regions, is the most numerous and widely distributed species preferring forest belt in the mountains of Kuznetskii Alatau (Kemerovskaya Oblast and Khakassia), North Altai (Republic of Altai) and West Altai (

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12

Aguilar-Argüello, Samuel, Francisco Díaz-Fleischer, and Dinesh Rao. "Motion-triggered defensive display in a tephritid fly." Journal of Ethology 34, no. 1 (2015): 31–37. http://dx.doi.org/10.1007/s10164-015-0442-8.

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13

Aguilar-Argüello, Samuel, Francisco Díaz-Fleischer, and Dinesh Rao. "Target-invariant aggressive display in a tephritid fly." Behavioural Processes 121 (December 2015): 33–36. http://dx.doi.org/10.1016/j.beproc.2015.10.006.

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14

Thibout, É., D. Pierre, N. Mondy, C. Lecomte, J. C. Biémont, and J. Auger. "Host-plant finding by the asparagus fly, Plioreocepta poeciloptera (Diptera: Tephritidae), a monophagous, monovoltine tephritid." Bulletin of Entomological Research 95, no. 5 (2005): 393–99. http://dx.doi.org/10.1079/ber2005370.

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AbstractThe role of various olfactory and visual stimuli was studied in host-plant finding by the asparagus fly Plioreocepta poeciloptera (Schrank), a monophagous monovoltine tephritid causing serious damage to asparagus spears. Volatiles released by asparagus plants were extracted by diethyl ether after cryotrapping concentration, and identified by gas chromatography–mass spectrometry. Twelve of the 13 compounds identified were tested using electroantennography to measure the response of the fly. Behavioural response was analysed using two different flight tunnels according to circadian rhyth

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15

Averill, Anne L., and Ronald J. Prokopy. "Intraspecific Competition in the Tephritid Fruit Fly Rhagoletis Pomonella." Ecology 68, no. 4 (1987): 878–86. http://dx.doi.org/10.2307/1938359.

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16

Sutton, Bruce D., and David A. Carlson. "Interspecific variation in tephritid fruit fly larvae surface hydrocarbons." Archives of Insect Biochemistry and Physiology 23, no. 2 (1993): 53–65. http://dx.doi.org/10.1002/arch.940230202.

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17

Willhoeft, Ute, and Gerald Franz. "Comparison of the mitotic karyotypes of Ceratitis capitata, Ceratitis rosa, and Trirhithrum coffeae (Diptera: Tephritidae) by C-banding and FISH." Genome 39, no. 5 (1996): 884–89. http://dx.doi.org/10.1139/g96-111.

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The sex chromosomes of the tephritid fruit fly Ceratitis capitata (Wiedemann) are heteromorphic. The male-determining region was located on the Y chromosome by deletion mapping using unbalanced offspring from several translocation strains. In addition, we showed that only 15% of the Y chromosome is required for male determination and male fertility. Based on this result, we expected to find Y-chromosomal length polymorphism in natural populations. Using fluorescence in situ hybridization with two repetitive DNA probes that label the Y chromosome, no obvious size differences were detected in se

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18

Follett, Peter A., Fay E. M. Haynes, and Bernard C. Dominiak. "Host Suitability Index for Polyphagous Tephritid Fruit Flies." Journal of Economic Entomology 114, no. 3 (2021): 1021–34. http://dx.doi.org/10.1093/jee/toab035.

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Abstract Tephritid fruit flies are major economic pests for fruit production and are an impediment to international trade. Different host fruits are known to vary in their suitability for fruit flies to complete their life cycle. Currently, international regulatory standards that define the likely legal host status for tephritid fruit flies categorize fruits as a natural host, a conditional host, or a nonhost. For those fruits that are natural or conditional hosts, infestation rate can vary as a spectrum ranging from highly attractive fruits supporting large numbers of fruit flies to very poor

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19

Zhao, J. T., M. Frommer, J. A. Sved, and A. Zacharopoulou. "Mitotic and polytene chromosome analyses in the Queensland fruit fly, Bactrocera tryoni (Diptera: Tephritidae)." Genome 41, no. 4 (1998): 510–26. http://dx.doi.org/10.1139/g98-053.

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The Queensland fruit fly, Bactrocera tryoni, like the Mediterranean fruit fly, Ceratitis capitata, has a diploid complement of 12 chromosomes, including five pairs of autosomes and a XX/XY sex chromosome pair. Characteristic features of each chromosome are described. Chromosomal homology between B. tryoni and C. capitata has been determined by comparing chromosome banding pattern and in situ hybridisation of cloned genes to polytene chromosomes. Although the evidence indicates that a number of chromosomal inversions have occurred since the separation of the two species, synteny of the chromoso

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20

Stark, John D., Roger I. Vargas, and Ronald K. Thalman. "Azadirachtin: Effects on Metamorphosis, Longevity, and Reproduction of Three Tephritid Fruit Fly Species (Diptera: Tephritidae)." Journal of Economic Entomology 83, no. 6 (1990): 2168–74. http://dx.doi.org/10.1093/jee/83.6.2168.

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21

Follett, Peter A., and John W. Armstrong. "Revised Irradiation Doses to Control Melon Fly, Mediterranean Fruit Fly, and Oriental Fruit Fly (Diptera: Tephritidae) and a Generic Dose for Tephritid Fruit Flies." Journal of Economic Entomology 97, no. 4 (2004): 1254–62. http://dx.doi.org/10.1093/jee/97.4.1254.

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22

Dias, Vanessa S., Guy J. Hallman, Olga Y. Martínez-Barrera, et al. "Modified Atmosphere Does Not Reduce the Efficacy of Phytosanitary Irradiation Doses Recommended for Tephritid Fruit Flies." Insects 11, no. 6 (2020): 371. http://dx.doi.org/10.3390/insects11060371.

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Phytosanitary irradiation (PI) has been successfully used to disinfest fresh commodities and facilitate international agricultural trade. Critical aspects that may reduce PI efficacy must be considered to ensure the consistency and effectiveness of approved treatment schedules. One factor that can potentially reduce PI efficacy is irradiation under low oxygen conditions. This factor is particularly important because storage and packaging of horticultural commodities under low oxygen levels constitute practices widely used to preserve their quality and extend their shelf life. Hence, internatio

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23

Suckling, David Maxwell, John M. Kean, Lloyd D. Stringer, et al. "Eradication of tephritid fruit fly pest populations: outcomes and prospects." Pest Management Science 72, no. 3 (2014): 456–65. http://dx.doi.org/10.1002/ps.3905.

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24

MANGEL, MARC, and BERNARD D. ROITBERG. "Dynamic information and host acceptance by a tephritid fruit fly." Ecological Entomology 14, no. 2 (1989): 181–89. http://dx.doi.org/10.1111/j.1365-2311.1989.tb00768.x.

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25

Yee, W. L. "Ambient light intensity and direction determine relative attractiveness of yellow traps toRhagoletis indifferens(Diptera: Tephritidae)." Canadian Entomologist 147, no. 6 (2015): 776–86. http://dx.doi.org/10.4039/tce.2015.6.

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AbstractUnderstanding factors that influence attraction of tephritid fruit flies (Diptera: Tephritidae) to objects can lead to development of more sensitive traps for fly detection. Here, the objective was to determine if differences in attractiveness between two sticky yellow rectangle traps to western cherry fruit fly,Rhagoletis indifferensCurran, depend on ambient light intensity and direction. The translucent plastic Yellow Sticky Strip (YSS) was compared with the less translucent yellow cardboard Alpha Scents (AS). Flies were released inside a box or cage opposite a trap or traps illumina

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Al Baki, Md Abdullah, Mohammad Vatanparast, and Yonggyun Kim. "Male-biased Adult Production of the Striped Fruit Fly, Zeugodacus scutellata, by Feeding dsRNA Specific to Transformer-2." Insects 11, no. 4 (2020): 211. http://dx.doi.org/10.3390/insects11040211.

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Sterile insect release technique (SIT) is effective for eradicating quarantine insects including various tephritid fruit flies. When SIT is used for fruit flies, it is challenging to remove females from sterile males due to oviposition-associated piercing damage. This study developed a sex transition technique by feeding double-stranded RNA (dsRNA) specific to a sex-determining gene, Transformer-2 (Zs-Tra2) of the striped fruit fly, Zeugodacus scutellata. Zs-Tra2 is homologous to other fruit fly orthologs. It is highly expressed in female adults. RNA interference (RNAi) of Zs-Tra2 by injecting

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27

Kean, J. M. "Metaanalysis validation and application of fruit fly development times." New Zealand Plant Protection 68 (January 8, 2015): 44–53. http://dx.doi.org/10.30843/nzpp.2015.68.5867.

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Tephritid fruit flies have been comparatively well studied because of the damage they cause to horticultural crops in affected countries New Zealand benefits from this knowledge as it continues to exclude economically damaging fruit fly species For example fruit fly development models are used for biosecurity risk analysis and decision making during incursion responses Here the literature was searched for development times for three species of particular concern to New Zealand the Mediterranean fruit fly the Queensland fruit fly and the oriental fruit fly The published data were reanalysed to

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28

Dodson, Gary. "Lek Mating System and Large Male Aggressive Advantage in a Gall-forming Tephritid Fly (Diptera: Tephritidae)." Ethology 72, no. 2 (2010): 99–108. http://dx.doi.org/10.1111/j.1439-0310.1986.tb00610.x.

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29

López-Ortega, Maurilio, Paulino Pérez-Rodríguez, Diana Pérez-Staples, and Francisco Díaz-Fleischer. "Patterns of Oviposition and Feeding in the Monophagous Fly Anastrepha spatulata (Diptera: Tephritidae) on its Larval Host Plant Schoepfia schreberi." Environmental Entomology 48, no. 5 (2019): 1178–86. http://dx.doi.org/10.1093/ee/nvz088.

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Abstract Monophagous insects that use discrete resources for oviposition and feeding are especially sensitive to variations in host quality and availability because their opportunities to find these resources are scarce. The monophagous tephritid fly Anastrepha spatulata Stone is a tephritid fly that uses as hosts the fruits of the non-economically important Schoepfia schreberi J. F. Gmel. Scant information of host utilization behavior in the field is available for this species. Wild individually marked flies were observed during the fruiting season. Observations of oviposition, feeding and re

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30

Averill, Anne L., W. Harvey Reissig, and Wendell L. Roelofs. "Specificity of olfactory responses in the tephritid fruit fly, Rhagoletis pomonella." Entomologia Experimentalis et Applicata 47, no. 3 (1988): 211–22. http://dx.doi.org/10.1111/j.1570-7458.1988.tb01139.x.

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31

Diaz-Fleischer, F., and J. Arredondo. "Light conditions affect sexual performance in a lekking tephritid fruit fly." Journal of Experimental Biology 214, no. 15 (2011): 2595–602. http://dx.doi.org/10.1242/jeb.055004.

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Abraham, Solana, M. Teresa Vera, and Diana Pérez-Staples. "Current Sperm Competition Determines Sperm Allocation in a Tephritid Fruit Fly." Ethology 121, no. 5 (2015): 451–61. http://dx.doi.org/10.1111/eth.12355.

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33

Jones, T. H., H. C. J. Godfray, and M. P. Hassell. "Relative movement patterns of a tephritid fly and its parasitoid wasps." Oecologia 106, no. 3 (1996): 317–24. http://dx.doi.org/10.1007/bf00334559.

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34

Wang, Xin-Geng, Ekhlass A. Jarjees, Benjamin K. McGraw, Aimé H. Bokonon-Ganta, Russell H. Messing, and Marshall W. Johnson. "Effects of spinosad-based fruit fly bait GF-120 on tephritid fruit fly and aphid parasitoids." Biological Control 35, no. 2 (2005): 155–62. http://dx.doi.org/10.1016/j.biocontrol.2005.07.003.

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35

Hanna, Rachid, Désiré Gnanvossou, Georg Goergen, et al. "Efficiency of Food-Based Attractants for Monitoring Tephritid Fruit Flies Diversity and Abundance in Mango Systems Across Three West African Agro-Ecological Zones." Journal of Economic Entomology 113, no. 2 (2019): 860–71. http://dx.doi.org/10.1093/jee/toz338.

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Abstract Food baits are effective and widely used tools for monitoring diversity and abundance of tephritid fruit flies. Four food-baits—Nulure, BioLure, Mazoferm at 3 and 6%, and Torula yeast—were used in multi-lure traps over a 4-yr period in mango orchards in three Benin agro-ecological zones (AEZ) representing a large swath of environments in western Africa. Twelve tephritid fruit fly species were captured during the trials, with the highest richness in the Forest Savannah Mosaic (FSM), followed by the Southern Guinea Savannah (SGS), and the Northern Guinea Savannah (NGS) AEZ. Despite prev

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Torrini, Giulia, Giuseppe Mazza, Claudia Benvenuti, and Pio Federico Roversi. "Susceptibility of olive fruit fly, Bactrocera oleae (Diptera: Tephritidae) pupae to entomopathogenic nematodes." Journal of Plant Protection Research 57, no. 3 (2017): 318–20. http://dx.doi.org/10.1515/jppr-2017-0030.

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Abstract The olive fruit fly Bactrocera oleae is one of the most serious and economically damaging insects worldwide, affecting the quality and quantity of both olive oil and table olives. Laboratory bioassays were conducted for the first time to evaluate the susceptibility of B. oleae pupae to two entomopathogenic nematodes (EPN) species, Steinernema carpocapsae and Heterorhabditis bacteriophora. The nematodes tested caused pupal mortality of 62.5% and 40.6%, respectively. The most noteworthy result was obtained with S. carpocapsae which was able to infect 21.9% of the emerged adults. Since t

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Yip, Eric C., István Mikó, Jonah M. Ulmer, et al. "Giant polyploid epidermal cells and male pheromone production in the tephritid fruit fly Eurosta solidaginis (Diptera: Tephritidae)." Journal of Insect Physiology 130 (April 2021): 104210. http://dx.doi.org/10.1016/j.jinsphys.2021.104210.

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Papadopoulos, Nikos T., Richard E. Plant, and James R. Carey. "From trickle to flood: the large-scale, cryptic invasion of California by tropical fruit flies." Proceedings of the Royal Society B: Biological Sciences 280, no. 1768 (2013): 20131466. http://dx.doi.org/10.1098/rspb.2013.1466.

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Since 1954, when the first tropical tephritid fruit fly was detected in California, a total of 17 species in four genera and 11 386 individuals (adults/larvae) have been detected in the state at more than 3348 locations in 330 cities. We conclude from spatial mapping analyses of historical capture patterns and modelling that, despite the 250+ emergency eradication projects that have been directed against these pests by state and federal agencies, a minimum of five and as many as nine or more tephritid species are established and widespread, including the Mediterranean, Mexican and oriental fru

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Meats, A., and A. D. Clift. "Zero catch criteria for declaring eradication of tephritid fruit flies: the probabilities." Australian Journal of Experimental Agriculture 45, no. 10 (2005): 1335. http://dx.doi.org/10.1071/ea04108.

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We examine procedures for declaring an area free of pest fruit flies following an eradication campaign. To date, the acceptable period of trapping zero flies has been calculated without an estimate of the probability of being wrong. The zero trapping periods are usually shorter when declaring local ‘area freedom’ from an endemic fly, than when claiming eradication of an exotic species. We use a model to calculate the probability of zero trap captures and therefore the probability of trapping further flies. The latter probability is always finite. A zero trapping result does not indicate the ab

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40

Anantanawat, Kay, Alexie Papanicolaou, Kelly Hill, and Wei Xu. "Molecular Response of the Mediterranean Fruit Fly (Diptera: Tephritidae) to Heat." Journal of Economic Entomology 113, no. 5 (2020): 2495–504. http://dx.doi.org/10.1093/jee/toaa147.

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Abstract Tephritid fruit flies are highly successful invaders and some—such as the Mediterranean fruit fly, Ceratitis capitata (Wiedemann)—are able to adapt to a large range of crops. Biosecurity controls require that shipments of produce are ensured to be pest-free, which is increasingly difficult due to the ban of key pesticides. Instead, stress-based strategies including controlled atmosphere, temperature, and irradiation can be used to eradicate flies inside products. However, unlike pesticide science, we do not yet have a robust scientific approach to measure cost-effectively whether a su

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Chang, Chiou Ling, and Peter Follett. "Resveratrol modifies tephritid fruit fly response to radiation but not nutritional stress." International Journal of Radiation Biology 88, no. 4 (2012): 320–26. http://dx.doi.org/10.3109/09553002.2012.647234.

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42

Tan, L. T., and K. H. Tan. "Automated tephritid fruit fly semiochemical mass feeding structure: design, construction and testing." Journal of Applied Entomology 137 (December 5, 2011): 217–29. http://dx.doi.org/10.1111/j.1439-0418.2011.01680.x.

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PAPAJ, D. R., and M. ALUJA A. "Temporal dynamics of host-marking in the tropical tephritid fly, Anastrepha ludens." Physiological Entomology 18, no. 3 (1993): 279–84. http://dx.doi.org/10.1111/j.1365-3032.1993.tb00600.x.

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GREENE, E., L. J. ORSAK, and D. W. WHITMAN. "A Tephritid Fly Mimics the Territorial Displays of Its Jumping Spider Predators." Science 236, no. 4799 (1987): 310–12. http://dx.doi.org/10.1126/science.236.4799.310.

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Diaz-Fleischer, F., J. Arredondo, and M. Aluja. "Enriching early adult environment affects the copulation behaviour of a tephritid fly." Journal of Experimental Biology 212, no. 13 (2009): 2120–27. http://dx.doi.org/10.1242/jeb.027342.

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Baker, P. S., and A. S. T. Chan. "Quantification of tephritid fruit fly dispersal: Guidelines for a sterile release programme." Journal of Applied Entomology 112, no. 1-5 (1991): 410–21. http://dx.doi.org/10.1111/j.1439-0418.1991.tb01074.x.

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Lavine, Barry K., David A. Carlson, and Carroll O. Calkins. "Classification of tephritid fruit fly larvae by gas chromatography/pattern recognition techniques." Microchemical Journal 45, no. 1 (1992): 50–57. http://dx.doi.org/10.1016/0026-265x(92)90070-j.

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Perez-Staples, Diana, and Martín Aluja. "Sperm allocation and cost of mating in a tropical tephritid fruit fly." Journal of Insect Physiology 52, no. 8 (2006): 839–45. http://dx.doi.org/10.1016/j.jinsphys.2006.05.007.

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Wang, X. G., and R. H. Messing. "Newly imported larval parasitoids pose minimal competitive risk to extant egg–larval parasitoid of tephritid fruit flies in Hawaii." Bulletin of Entomological Research 92, no. 5 (2002): 423–29. http://dx.doi.org/10.1079/ber2002181.

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Abstract:

AbstractCompetitive displacement of fruit fly parasitoids has been a serious issue in the history of fruit fly biological control in Hawaii. This concern regarding competitive risk of new parasitoids has led to an overall tightening of regulations against the use of classical biological control to manage fruit flies. Fopius arisanus (Sonan), an egg–larval parasitoid, is the most effective natural enemy of tephritid fruit flies in Hawaii. This study evaluated the competitive risk of two recently introduced larval parasitoids, Diachasmimorpha kraussii Fullaway and Psyttalia concolor (Szépligeti)

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Purcell, M. F., J. J. Duan, and R. H. Messing. "Response of Three Hymenopteran Parasitoids Introduced for Fruit Fly Control to a Gall-Forming Tephritid,Procecidochares alani(Diptera: Tephritidae)." Biological Control 9, no. 3 (1997): 193–200. http://dx.doi.org/10.1006/bcon.1997.0533.

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