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Articles de revues sur le sujet « Fruit piercing moth »

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Auteur : Grafiati
Publié le 7 septembre 2023

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1

Fay, HA C. « Evolutionary and taxonomic relationships between fruit-piercing moths and the Menispermaceae ». Australian Systematic Botany 9, no 2 (1996) : 227. http://dx.doi.org/10.1071/sb9960227.

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Twining vines of the family Menispermaceae provide the food for larvae of the principal fruit-piercing moths in Australia, and in most of the Old World tropics and near tropics. These large noctuid moths are adult pests of a range of commercial fruits, and can cause crop losses of more than 50%. In Australia, the Menispermaceae are represented by 13 genera and 24 species, which predominantly occur through coastal and subcoastal regions in the east and north of the continent. Their density and diversity is greatest in the wet tropical forest areas of north-east Queensland. Around 60% of the Australian menisperm species are now known to support fruit-piercing moth larvae to various extents. While moth species-menisperm associations range from species specific (i.e. monophagy) to genera generalist (i.e. polyphagy), polyphagy appears to contribute less to a moth's status as a pest than habitat diversity. Tinospora smilacina and Stephania japonica are the two most widely occurring Australian menisperms, with forms or varieties occupying habitats from wet tropical forest to semi-desert, and these species are particularly important to the fruit-piercing moth problem. Some moth species-host plant associations appear to be dynamic, as indicated by the dietary expansion of the moth Othreis fullonia in recent centuries onto Erythrina spp. (Fabaceae) in New Guinea and the Pacific. The perceived relationship between Erythrina spp. and the Menispermaceae is through the similar alkaloids they possess (i.e. the tetracyclic Erythrina-type), which are found particularly in certain species within the tribe Menispermeae. Variation in the alkaloids associated with certain menisperm genera may explain specific moth–host plant relationships, which in turn support alternative tribal associations for some menisperm taxa to those currently recognised.
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2

MAGAR, P. N., S. R. KULKARNI et A. G. CHANDELE. « Natural parasitoids of fruit piercing moth, Eudocima spp. » Journal of Biological Control 31, no 1 (9 décembre 2017) : 10–12. http://dx.doi.org/10.18311/jbc/2017/15557.

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3

Reddy, G. V. P., Z. T. Cruz, J. Bamba et R. Muniappan. « Host adaptation of the fruit piercing moth, Eudocima fullonia ». Physiological Entomology 30, no 4 (17 juin 2005) : 398–401. http://dx.doi.org/10.1111/j.1365-3032.2005.00465.x.

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4

Kamala, Jayanthi PD, AM Ravindra et Vivek Kempraj. « Pomegranate fruits damaged by conspecifics attract fruit piercing moth eudocima materna (L.) ». Indian Journal of Entomology 82, no 4 (2020) : 681–87. http://dx.doi.org/10.5958/0974-8172.2020.00092.9.

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5

Leong, Stephen Chan Teck, et Roland Jui Heng Kueh. « Seasonal Abundance and Suppression of Fruit-Piercing MothEudocima phalonia(L.) in a Citrus Orchard in Sarawak ». Scientific World JOURNAL 11 (2011) : 2330–38. http://dx.doi.org/10.1100/2011/753484.

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Seasonal population of the fruit-piercing mothsEudocimaspp. was monitored throughout the citrus growing seasons in a citrus orchard and in site adjacent to secondary forest from July 2007 to June 2009. The moth was detected practically throughout the year with activity lowest during the wet months (September-February) when fruits are still available and while highest during the dry months (May-June) which also coincided with the main fruiting season. The effects of annC24 horticultural mineral oil (HMO) on the citrus fruit damage caused by fruit-piecing moths was also determined. The percent fruit damage was significantly lowest (P≤0.05) in HMO-treated plots (8.4), followed by Dimethoate-treated plots (11.6) and untreated plots (22.5). However, there was no significant difference between HMO and Dimethoate treated plots indicating HMO is effective in reducing percent fruit damage.
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6

Reddy, G. V. P., Z. T. Cruz et R. Muniappan. « Attraction of fruit-piercing moth Eudocima phalonia (Lepidoptera : Noctuidae) to different fruit baits ». Crop Protection 26, no 4 (avril 2007) : 664–67. http://dx.doi.org/10.1016/j.cropro.2006.06.004.

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7

Hilgartner, Roland, Mamisolo Raoilison, Willhelm Büttiker, David C. Lees et Harald W. Krenn. « Malagasy birds as hosts for eye-frequenting moths ». Biology Letters 3, no 2 (4 janvier 2007) : 117–20. http://dx.doi.org/10.1098/rsbl.2006.0581.

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While tear-feeding in moths on mammals is widespread, there have been no reports of this behaviour in Madagascar and none on birds. We report that a moth, Hemiceratoides hieroglyphica belonging to the Calpini, a generally fruit-feeding or blood-feeding lineage of noctuids, attacks sleeping birds in Madagascar. This moth is able to intrude its sharply tipped proboscis into a closed bird's eye. The proboscis is characterized by a specific armoury of hooks, barbs and spines similar to that in piercing calpines but dissimilar to that in other tear-feeding moths. This is the first report of exploitation of tears by Lepidoptera from the closed eyes of sleeping birds.
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8

Adarsh P.K et Abhilash Peter. « First report of Eudocima cajeta (Cramer) (Lepidoptera : Erebidae) from Kerala, India with notes on male and female genitalia ». Ecology, Environment and Conservation 29, no 02 (2023) : 703–6. http://dx.doi.org/10.53550/eec.2023.v29i02.025.

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A report on the fruit piercing moth Eudocima cajeta (Cramer) (Lepidoptera: Erebidae) is authenticated for the first time from Kerala, India. In addition to the morphology of the adults, detailed notes on the male and female genitalia structures are also provided in this paper.
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9

Muniappan, R., I. U. Silva-Krott et T. S. Lali. « Distribution of larval host plants of the fruit piercing moth,Othreis fullonia ». Chemoecology 5-6, no 2 (juin 1994) : 75–77. http://dx.doi.org/10.1007/bf01259435.

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10

Goddard, M., M. P. Hill et S. D. Moore. « An Analysis of the Fruit-Sucking and Fruit-Piercing Moth Complex in Citrus Orchards in South Africa ». African Entomology 27, no 1 (25 avril 2019) : 1. http://dx.doi.org/10.4001/003.027.0001.

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Izumi, Yohei, Ruilin Tian, Shoji Sonoda, Yuriko Imayoshi, Hisakatsu Iwabuchi, Yuji Miyashita, Shuji Kanazaki et Hisaaki Tsumuki. « Analysis of peach fruit headspace volatiles and response by the fruit-piercing moth Oraesia excavata (Lepidoptera : Noctuidae) ». Applied Entomology and Zoology 50, no 2 (25 février 2015) : 231–38. http://dx.doi.org/10.1007/s13355-015-0330-2.

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OHMASA, Yoshihisa, Sadao WAKAMURA, Shuji KOZAI, Hajime SUGIE, Michio HORIIKE, Chisato HIRANO et Sukekazu MORI. « Sex Pheromone of the Fruit-Piercing Moth, Oraesia excavata(BUTLER)(Lepidoptera:Noctuidae):Isolation and Identification ». Applied Entomology and Zoology 26, no 1 (1991) : 55–62. http://dx.doi.org/10.1303/aez.26.55.

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13

Sivasankaran, Kuppusamy, Pratheesh Mathew, Sekar Anand, Stanislaus Antony Ceasar, Soosaimanikam Mariapackiam et Savarimuthu Ignacimuthu. « Complete mitochondrial genome sequence of fruit-piercing moth Eudocima phalonia (Linnaeus, 1763) (Lepidoptera : Noctuoidea) ». Genomics Data 14 (décembre 2017) : 66–81. http://dx.doi.org/10.1016/j.gdata.2017.09.004.

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Tian, Ruilin, Yohei Izumi, Shoji Sonoda, Hideya Yoshida, Takuma Takanashi, Kiyoshi Nakamuta et Hisaaki Tsumuki. « Electroantennographic responses and field attraction to peach fruit odors in the fruit-piercing moth, Oraesia excavata (Butler) (Lepidoptera : Noctuidae) ». Applied Entomology and Zoology 43, no 2 (2008) : 265–69. http://dx.doi.org/10.1303/aez.2008.265.

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15

Zaspel, Jennifer M., Vladimir S. Kononenko, Rickard Ignell et Sharon R. Hill. « Host-Related Olfactory Behavior in a Fruit-Piercing Moth (Lepidoptera : Erebidae) in Far Eastern Russia ». Journal of Insect Science 16, no 1 (2016) : 51. http://dx.doi.org/10.1093/jisesa/iew037.

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16

Leroy, Lise, Christian Mille et Bruno Fogliani. « The Common Fruit-Piercing Moth in the Pacific Region : A Survey of the Current State of a Significant Worldwide Economic Pest, Eudocima phalonia (Lepidoptera : Erebidae), with a Focus on New Caledonia ». Insects 12, no 2 (29 janvier 2021) : 117. http://dx.doi.org/10.3390/insects12020117.

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When referring to fruit-piercing moths, the genus Eudocima, and more specifically Eudocima phalonia (Linneaus), is cited as a worldwide crop pest. Damages associated with this pest are substantial on more than 100 fruit species, wherever it is encountered. In New Caledonia, the once occasional pest has become a serious threat to the current fruit arboriculture. Particularly devastating during outbreak periods, it has become an urgent need to find a suitable solution able to support farmers in the ecological transition of our agricultural models. This review proposes a synthesis of the existing data and publications on E. phalonia, worldwide and especially in New Caledonia, with recent observations. The assessment of this knowledge and the dynamics of the species in the territory of New Caledonia provide key information for a better prospect of adapted solutions.
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17

Dharmayanthi, A. B., E. Arida, Darmawan, S. Y. Wiyati, T. Haryoko, M. S. A. Zein et H. Sutrisno. « Reassessment on the monophyly of the fruit-piercing moth, Eudocima bilberg, 1820 (Lepidoptera : Erebidae) using molecular data ». IOP Conference Series : Earth and Environmental Science 948, no 1 (1 décembre 2021) : 012030. http://dx.doi.org/10.1088/1755-1315/948/1/012030.

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Abstract Eudocima Billberg, 1820 is a group of moths known for their fruit-piercing behaviour. Members of this group are easily distinguished for their bright colour, hind wing patterns, and the robustness of their body. However, the monophyly of this genus is still in dispute. Based on morphological characters, a current study on 48 species of this genus showed that Eudocima is not a monophyletic group. We conducted a preliminary analysis of 25 species of Eudocima based on 632-bp sequences of cytochrome oxidase 1 (COI) to reassess the monophyly of this genus. Using Maximum Parsimony (MP) method, we ran a number of data sets to reconstruct the most appropriate phylogenetic tree. The result showed that Eudocima is a monophyletic group based on a nucleotide weighting of transversion: transitions = 2:1, despite the very low Jackknife support. This result should not be taken as a final conclusion because only about 60% of Eudocima species were included in our analysis. An upcoming study involving all members of this genus is necessary in order to reassess the putative monophyly of this genus.
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18

Shendge, Eknath, Bapurao Khaire et Ramrao Chavan. « A study on biology and larval behaviour of fruit piercing moth of Othreis (Eudocima) materna (L.) (Lepidoptera : Noctuidae) on pomegranate, Punica granatum ». Journal of Applied and Natural Science 13, no 1 (25 février 2021) : 178–82. http://dx.doi.org/10.31018/jans.v13i1.2489.

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Among different fruit piercing moths, the genus Othreis are the most harmful, causing widespread damage to pomegranate, citrus and mango fruits causing fruit fall in tropical and subtropical countries. The present communication deals with the study on the biology of Othreis materna (L) from egg to adult’s death which was carried out at room temperature of the laboratory to investigate the delicate and vulnerable stages of its life cycle. The life cycle of the moth was completed within 45-61 days, with an average 55.03 days in case of male and within 47-63 days with an average 57.07±4.92 in case of female. Eggs hatching started at night or early in the morning and duration of hatching was 2.72 days. The eggs measured were about 0.95 to 0.03 mm in diameter. The freshly emerged first instar larvae were light yellowish coloured and translucent. The first instar larvae were very active after hatching and they moved 4 to 6 feet for searching the food. The larvae were fed with the leaves of Tinospora cordifolia (Giloy or Guduchi). The total larval duration in days from first, second, third, fourth and fifth instar varied from 2.12±0.01, 1.81±0.05, 2.87±0.02, 3.90±0.11, 4.74±0.38 in days respectively and total larval period was 15.44±0.57. Pupae were dark brown in colour and total pupation period was of 13.81±0.12 days and total adult duration for male and female was 23.08±0.70 and 25.20±0.66 days respectively. The adult of O. materna was bright orange in colour and of medium size. The male was small than the female. This is first study of this type from Marathwada, which will help to trace the vulnerable and delicate stage of the life cycle of this O. materna.
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19

Agasyeva, Irina. « Ectoparasite Habrobracon Hebetor Say Is an Efficient Biological Control Agent of Lepidopteran Pests ». E3S Web of Conferences 285 (2021) : 03010. http://dx.doi.org/10.1051/e3sconf/202128503010.

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Ectoparasite Habrobracon hebetor Say is one of the most widely used biological controllers in biological plant protection against a number of harmful lepidopterans, including especially dangerous pests of corn, soy, fruit and vegetable crops. As a result of research conducted in 2017, food specialization and parasitic activity of three different populations of H.hebetor were studied. Two races have been identified for mass rearing and application: pyralid and leaf roller (against corn moth, bean pod borer, apple and plum moths), and pyralid owl-moth (against cotton moth, corn borer, bean pod borer and boxwood moth). As a result of studies of biological features and trophic needs, it has been determined that caterpillars of mill moth (Ephestia cuhniellia Zella) should be used as a host insect for laboratory cultivation of the stock population of the Habrobracon pyralid and leaf roller race (race No. 1). For the introduced from South Kazakhstan the H.hebetor pyralid and noctuid race the most productive rearing is on the caterpillars of large bee moth (Galleria mellonela L.). Optimal temperature for rearing of both races is 26-28 ° C, relative air humidity is 70% and photoperiod is not less than 16 hours. It has been noticed that before laying eggs on the host’s caterpillars, the Habrobracon female preliminarily paralyzes the victim, piercing the sheath with ovipositor. As a result, the caterpillar stops eating and is immobilized. In 3-4 days larvae hatch out of the laid on the caterpillar eggs. The larvae feed on the contents of the caterpillars for 4-5 days, then pupate and after 6-8 days an adult insect leaves the cocoon. The development of one generation lasts 13-16 days, one cocoon includes one parasite. 1,000 large bee moth caterpillars used for infection provide on average 5.8-6.0 thousand cocoons, of which an average of 4.5-4.7 thousand parasites fly out.
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Sands, D. P. A., M. Schotz et A. S. Bourne. « Effects of temperature on development and seasonality of Eudocima salaminia (Lepidoptera : Noctuidae) in eastern Australia ». Bulletin of Entomological Research 81, no 3 (septembre 1991) : 291–96. http://dx.doi.org/10.1017/s0007485300033563.

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AbstractThe durations for development for immature stages of the fruit piercing moth, Eudocima salaminia (Cramer), were determined at constant temperatures ranging from 15°C to 27°C and at ambient temperatures at a field site in southeastern Queensland over a 16 month period. At constant temperatures average heat requirements for: 50% eclosion of eggs were 62.4 day-degrees above 11°C, development of larvae to pupation were 246 day-degrees above 12°C, development of pupae to eclosion were 233 day-degrees above 12°C. For each stage there was no difference between day-degrees calculated at constant temperatures or at those in the field indicating no diapause in the immature stages. For adults, temperatures below 16°C during the activity period after dusk prevented feeding, mating and oviposition. Failure of E. salaminia to overwinter in south-eastern Australia in most years, was explained by the effects of low temperatures on egg hatch, larval, pupal and adult survival, reduced adult feeding, mating and cessation of oviposition.
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Muniappan, R., Jesse Bamba, Junard Cruz et G. V. P. Reddy. « Biology, rearing and field release on Guam of Euplectrus maternus, a parasitoid of the fruit-piercing moth, Eudocima fullonia ». BioControl 49, no 5 (octobre 2004) : 537–51. http://dx.doi.org/10.1023/b:bico.0000036439.74117.2f.

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BROU JR., V. A., et A. ZILLI. « An overlooked sibling of the fruit-piercing moth Eudocima phalonia (Linnaeus, 1763) from Africa (Lepidoptera, Erebidae, Calpinae) ». Zootaxa 4109, no 3 (9 mai 2016) : 391. http://dx.doi.org/10.11646/zootaxa.4109.3.9.

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Zaspel, J. M., V. S. Kononenko et P. Z. Goldstein. « Another Blood Feeder ? Experimental Feeding of a Fruit-Piercing Moth Species on Human Blood in the Primorye Territory of Far Eastern Russia (Lepidoptera : Noctuidae : Calpinae) ». Journal of Insect Behavior 20, no 5 (10 juillet 2007) : 437–51. http://dx.doi.org/10.1007/s10905-007-9090-3.

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Klem, Crystal C., et Jennifer Zaspel. « Pest Injury Guilds, Lepidoptera, and Placing Fruit-Piercing Moths in Context : A Review ». Annals of the Entomological Society of America 112, no 5 (8 juillet 2019) : 421–32. http://dx.doi.org/10.1093/aesa/saz031.

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Abstract The pest status of insects in agricultural settings is human-defined based on behaviors that may negatively impact the yield of susceptible crops. As such, both the insect behavior and the affected crop play a part in determining pest status. One helpful means of understanding pest status involves using pest injury guilds, which distinguish different pest groups based on similar kinds of injury to comparable plant tissues. Pest injury guilds defined in the literature are reviewed and then applied to agriculturally significant Lepidoptera. More specialized Lepidoptera behaviors which are economically relevant, such as leaf-rolling or stem-boring, are examined within their respective injury guilds. In this review, fruit-piercing moths are discussed within the context of pest Lepidoptera behaviors and are highlighted due to their unique means of causing economic damage. Unlike other Lepidoptera in agricultural settings, fruit-piercing moths are harmful as adults rather than larvae, and directly injure fruits using a specially adapted proboscis. The ecology and systematics of fruit-piercing moths, as well as current control options, are also discussed.
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Shendge, E. S., et R. J. Chavan. « Review on fruit piercing moths of the genus Othreis ». Indian Journal of Entomology 81, no 4 (2019) : 712. http://dx.doi.org/10.5958/0974-8172.2019.00185.8.

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Nishino, Minoru, Ken Suzuki, Masami Takeuchi, Masahiko Tanaka et Keita Onaka. « Control of fruit-piercing moths on citrus fields by yellow LED ». Annual Report of The Kansai Plant Protection Society 57 (2015) : 73–76. http://dx.doi.org/10.4165/kapps.57.73.

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Hernández-Ruiz, Artemio, Carlos Patricio Illescas-Riquelme, Néstor Bautista-Martínez, Reyna Vargas-Abasolo, Jorge M. Valdez-Carrasco et Pedro Figueroa-Castro. « Identification of Fruit-Piercing Moths (Lepidoptera : Erebidae) and Damage Caused to Papaya Fruit in Mexico ». Entomological News 126, no 5 (avril 2017) : 415–20. http://dx.doi.org/10.3157/021.126.0511.

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Pathre, Ravindra Fakirrao, et Sharad Devidasrao Jadhav. « Some fruit piercing moths (Lepidoptera : Heterocera) from Jalna district of Maharashtra, India ». Journal of Entomological Research 44, no 1 (2020) : 131. http://dx.doi.org/10.5958/0974-4576.2020.00024.9.

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Vargas-Fonseca, Sergio, Yenny Correa-Carmona, José Mauricio Montes-Rodríguez, Humberto Calero-Mejía et Alberto Zilli. « Synopsis of fruit-piercing moths of the genus Eudocima (Lepidoptera, Erebidae) from Colombia ». ZooKeys 953 (27 juillet 2020) : 85–104. http://dx.doi.org/10.3897/zookeys.953.50709.

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In order to provide information about the diversity and distribution of Eudocima species in Colombia, 261 specimens deposited in entomological collections were examined and identified. We found seven of the eight species of Eudocima recorded in the Neotropics: E. anguina, E. colubra, E. collusoria, E. memorans and E. serpentifera, all being recorded for the first time from the country. We provide a list of the species, comments on the biology and distribution data, illustrations of the adults, and keys for species identification.
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Fay, H. A. C., et K. H. Halfpapp. « Fruit maturity and soundness relevant to feeding choice by fruit-piercing moths (Lepidoptera : Noctuidae) in citrus crops in northeast Australia ». International Journal of Pest Management 52, no 4 (octobre 2006) : 317–24. http://dx.doi.org/10.1080/09670870600834499.

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Zenker, Maurício Moraes, Marcos Botton, José Augusto Teston et Alexandre Specht. « Noctuidae moths occurring in grape orchards in Serra Gaúcha, Brazil and their relation to fruit-piercing ». Revista Brasileira de Entomologia 54, no 2 (juin 2010) : 288–97. http://dx.doi.org/10.1590/s0085-56262010000200012.

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Tian, Ruilin, Yohei Izumi, Shoji Sonoda, Hideya Yoshida, Takehiko Fukumoto, Tetsuo Saito et Hisaaki Tsumuki. « Estimation of repellency of a volatile compound, sec-butyl .BETA.-styryl ketone, against fruit-piercing moths ». Applied Entomology and Zoology 42, no 3 (2007) : 433–37. http://dx.doi.org/10.1303/aez.2007.433.

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Zaspel, J. M., R. Zahiri, M. A. Hoy, D. Janzen, S. J. Weller et N. Wahlberg. « A molecular phylogenetic analysis of the vampire moths and their fruit-piercing relatives (Lepidoptera : Erebidae : Calpinae) ». Molecular Phylogenetics and Evolution 65, no 2 (novembre 2012) : 786–91. http://dx.doi.org/10.1016/j.ympev.2012.06.029.

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Fay, Hac, et Kh Halfpapp. « Activity of fruit-piercing moths, Eudocima spp. (Lepidoptera : Noctuidae), in north Queensland crops : Some effects of fruit type, locality and season ». Australian Journal of Entomology 38, no 1 (février 1999) : 16–22. http://dx.doi.org/10.1046/j.1440-6055.1999.00072.x.

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Jones, P., et DPA Sands. « Euplectrus melanocephalus Girault (Hymenoptera : Eulophidae), an ectoparasitoid of larvae of fruit-piercing moths (Lepidoptera : Noctuidae : Catocalinae) from northern Queensland ». Australian Journal of Entomology 38, no 4 (novembre 1999) : 377–81. http://dx.doi.org/10.1046/j.1440-6055.1999.00113.x.

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Zaspel, Jennifer M., S. J. Weller et M. A. Branham. « A comparative survey of proboscis morphology and associated structures in fruit-piercing, tear-feeding, and blood-feeding moths in Calpinae (Lepidoptera : Erebidae) ». Zoomorphology 130, no 3 (2 août 2011) : 203–25. http://dx.doi.org/10.1007/s00435-011-0132-1.

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« Eudocima fullonia (fruit-piercing moth) ». CABI Compendium CABI Compendium (7 janvier 2022). http://dx.doi.org/10.1079/cabicompendium.23012.

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This datasheet on Eudocima fullonia covers Identity, Overview, Distribution, Dispersal, Hosts/Species Affected, Diagnosis, Biology & Ecology, Natural Enemies, Impacts, Prevention/Control, Further Information.
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« Gonodonta incurva (fruit-piercing moth) ». CABI Compendium CABI Compendium (7 janvier 2022). http://dx.doi.org/10.1079/cabicompendium.25691.

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« Oraesia emarginata (fruit piercing moth) ». CABI Compendium CABI Compendium (7 janvier 2022). http://dx.doi.org/10.1079/cabicompendium.37739.

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« Ophiusa coronata (fruit piercing moth) ». CABI Compendium CABI Compendium (7 janvier 2022). http://dx.doi.org/10.1079/cabicompendium.37568.

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« Eudocima fullonia (fruit-piercing moth) ». PlantwisePlus Knowledge Bank Species Pages (7 janvier 2022). http://dx.doi.org/10.1079/pwkb.species.23012.

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« Eudocima materna (fruit piercing moth) ». CABI Compendium CABI Compendium (7 janvier 2022). http://dx.doi.org/10.1079/cabicompendium.23015.

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« Ophiusa tirhaca (fruit piercing moth) ». CABI Compendium CABI Compendium (7 janvier 2022). http://dx.doi.org/10.1079/cabicompendium.37575.

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« Eudocima salaminia (fruit piercing moth) ». CABI Compendium CABI Compendium (7 janvier 2022). http://dx.doi.org/10.1079/cabicompendium.23017.

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« Oraesia excavata (fruit piercing moth) ». CABI Compendium CABI Compendium (7 janvier 2022). http://dx.doi.org/10.1079/cabicompendium.37740.

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Rajeshkanna, S., et P. Attputhachandran. « Fruit piercing moth on guava-Sri Lanka ». PlantwisePlus Knowledge Bank Pest Management (janvier 2015). http://dx.doi.org/10.1079/pwkb.20177800178.

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Mas, Flore, Rachael Horner, Lee-anne Manning, Aimee Harper, Sam Brierley, Stefano DeFaveri, Lise Leroy et Christian Mille. « Differential olfactory responses associated with host plant shift by the fruit-piercing moth, Eudocima phalonia, in the Pacific islands ». New Zealand Journal of Crop and Horticultural Science, 22 juin 2023, 1–15. http://dx.doi.org/10.1080/01140671.2023.2221859.

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Kumar, K. Kiran, A. George, G. T. Behere, Yogesh E. Thorat, Datta Ingle et Dharmendra P. Sinh. « Pathogenicity of Heterorhabditis indica against developmental stages of Eudocima materna L. (Lepidoptera, Erebidae) ». Egyptian Journal of Biological Pest Control 32, no 1 (4 juin 2022). http://dx.doi.org/10.1186/s41938-022-00563-1.

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Abstract Background Virulence of the entomopathogenic nematode, Heterorhabditis indica against larvae (3rd, 4th and 5th larval instars) and pupae of citrus fruit piercing moth, Eudocima materna L. (Lepidoptera: Erebidae) was evaluated under laboratory conditions. The experiments included pathogenicity assessment of H. indica against larvae and pupae using a range of concentrations (10, 25, 50, 100 and 200 infective juveniles (IJs) larva−1 and pupa−1) as well as evaluation of their reproductive potential on different larval instars with different concentrations (50, 100, 200, 400 and 600 IJs larva−1). Results Application of increasing concentrations of IJs induced higher mortality on larval instars and pupae with mean mortality ranging from 26.6 to 100% (LC50- 3rd (14.43 IJs larva−1), 4th (17.08 IJs larva−1), 5th (23.63 IJs larva−1)) and 10–70% (LC50- 85.91 IJs pupa−1) after 48 h post-exposure, respectively. H. indica successfully reproduced in the 3rd, 4th and 5th larval instars of E. materna and their offspring emerged from the cadavers. The highest reproduction was recorded in 5th instar larvae (1,082,855 IJs larva−1) at 600 IJs larva−1 in E. materna. Conclusion The present study suggests that H. indica strain had the potential for biological control of E. materna.
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Badii, B. K., et A. Cudjoe. « Fruit piercing moths on citrus-Ghana ». PlantwisePlus Knowledge Bank Pest Management (janvier 2016). http://dx.doi.org/10.1079/pwkb.20177800140.

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A. S. Mohite C.K. Deshmukh, A. S. Mohite C. K. Deshmukh. « POPULATION DENSITY OF FRUIT PIERCING MOTHS OF GENUS OTHREIS AND EXTENT OF DAMAGE IN THE ORANGE ORCHARDS OF VIDARBHA REGION OF MAHARASHTRA ». International Journal of Researches in Biosciences and Agriculture Technology, 2014. http://dx.doi.org/10.29369/ijrbat.2014.02.ii.0056.

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