First Record of Aphis Craccivora Koch (Hemiptera: Aphididae) on Aronia Crop in Montenegro
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Hellenic Plant Protection Journal 10: 67-69, 2017 DOI 10.1515/hppj-2017-0007 SHORT COMMUNICATION First record of Aphis craccivora Koch (Hemiptera: Aphididae) on aronia crop in Montenegro N. Latinović1, F. Karamaouna2 and N.G. Kavallieratos3* Summary The aphid Aphis craccivora was recorded on the crop of aronia, Aronia melanocarpa, in Montenegro, in June 2015 and 2016. This is the fi rst record of A. craccivora in Montenegro on aronia. Additional keywords: aphid, Aphis craccivora, Aronia melanocarpa, southeastern Europe In recent years aronia, Aronia melanocarpa titudes between 1063 m and 1077 m. They (Michx.) Elliott (Rosales: Rosaceae), has be- were spotted on two plants among a total of come a quite popular fruit crop in Monte- 1600 bushes. One year later, in June 2016, the negro. It is a woody perennial shrub, resis- presence of aphids was recorded on numer- tant to cold and can be successfully grown ous bushes of aronia among a total of 3000 in conditions of severe continental climate plants at the locality Stevanovac of the same (Nikolić and Milivojević, 2010), which domi- Municipality at altitudes between 875 m and nates in the northern part of Montenegro. It 905 m. Samples of aphids were collected in is currently considered as a profi table crop 2016 and were identifi ed as Aphis craccivora due to a relatively high price of the fruit Koch (Hemiptera: Aphididae). To our know- (black chokeberries) and its other uses, in- legde, this is the fi rst record of A. craccivora cluding processed products (i.e., syrup, infesting aronia in Montenegro. Aphids have juice, soft spreads, tea, food colors) (McKay, been previously reported as pests of aro- 2001) and as an ornamental plant (Yovkova nia (infestation of shoot tips) but the conse- et al., 2013). For all these reasons and the fact quent slow down eff ect on the plant growth that it is attacked by a small number of pests is not considered serious because the plants and diseases, aronia has earned a profound are vigorous (McKay, 2001). Recently, Aphis place in the organic production in Montene- spiraecola Patch (Hemiptera: Aphididae) gro, where among the total number of 203 and Aulacorthum circumfl exum (Buckton) registered organic producers, 20 of them (Hemiptera: Aphididae) were identifi ed as grow aronia berries at a surface area of ap- pests of A. melanocarpa from southeastern proximately 10 ha. Europe (Bulgaria) (Yovkova et al., 2013). In June 2015, at the locality of Bojna Nji- Aphis craccivora is a relatively small spe- va, Municipality of Mojkovac, aphids were cies. The apterous viviparous female individ- observed to infest an aronia plantation at al- uals have a shiny black or dark brown body with a prominent cauda and brown to yel- low legs. The immatures are slightly dust- 1 University of Montenegro, Biotechnical Faculty, Mi- ed with wax while adults appear without haila Lalića 15, Podgorica, Montenegro. wax. The antennae have six segments. The 2 Benaki Phytopathological Institute, 8 St. Delta Str., GR-145 61 Kifi ssia, Attica, Greece. distal part of femur, siphunculi and cauda 3 Agricultural University of Athens, Department of are black. The length of apterae individuals Crop Science, 75 Iera Odos Str., GR-118 55, Athens, At- tica, Greece. ranges between 1.4 and 2.2 mm. The alate * Corresponding author: [email protected] viviparous A. craccivora females have abdo- © Benaki Phytopathological Institute 68 Latinović et al. men with dorsal cross bars. The length of al- Aphidius colemani Viereck, Aphidius matri- atae ranges between 1.4 and 2.1 mm (Black- cariae Haliday, Binodoxys acalephae (Mar- man and Eastop, 2000). shall), Binodoxys angelicae (Haliday), Diaer- Aphis craccivora is associated with about etiella rapae (M’Intosh), Ephedrus pericae 50 crops and weed species belonging to 19 Froggat, Lipolexis gracilis Förster, Lysiphle- plant families (i.e., Amaranthaceae, Araceae, bus confusus Tremblay and Eady, Lysiphle- Asteraceae, Brassicaceae, Caryophyllaceae, bus fabarum (Marshall), Lysiphlebus orientalis Chenopodiaceae, Cucurbitaceae, Fabaceae, Starý and Rakhshani, Lysiphlebus testaceipes Malpighiaceae, Malvaceae, Nyctaginaceae, (Cresson), Praon abjectum (Haliday), Praon Pedaliaceae, Portulacaceae, Ranunculaceae, volucre (Haliday). Important predators in- Rosaceae, Rutaceae, Solanaceae, Sterculi- clude coccinellid beetles [Cheilomenes sex- aceae, Zingiberaceae) from which the aphid maculata (F.), Coccinella septempunctata (L.) mainly attacks Fabaceae (Blackman and Eas- (Coleoptera: Coccinelidae)], syrphid larvae top, 2007; Kavallieratos et al., 2007; Mehrpar- [Ischiodon scutellaris (F.) (Diptera: Syrphidae)] var et al., 2012; Yovkova et al., 2013; CABI data Neuroptera larvae [Micromus timidus Ha- base, 2016). The species is probably palearc- gen (Neuroptera: Hemerobiidae)] and Dip- tic warm temperate in origin but it has now tera larvae [Aphidoletes aphidimyza (Ron- a cosmopolitan distribution; it is abundant dani) (Diptera: Cecidomyidae)]. Spiders may in subtropical and tropical regions, and in also be important in some areas (CABI data the Mediterranean. It is one of the common- base, 2016). Recorded fungal pathogens in- est aphid species with a high pest status in clude Fusarium pallidoroseum (Cooke) Sacc. the tropics (Blackman and Eastop, 2000). (Hypocreales: Nectriaceae) (Hareendranath Aphis craccivora is generally anholocy- et al., 1987) and Neozygites fresenii (Nowak.) clic (wingless and winged females), ovovi- Remaud. and S. Keller (Entomophthorales: viparous. In the tropics the aphid reproduc- Neozygitaceae) (Zhang, 1987; Sewify, 2000). es parthenogenetically throughout the year Most of the major chemical groups of in- while in areas with colder winters, overwin- secticides have been used against this aphid tering may be as egg or hibernation. In Eu- species, including organophosphates, car- rope, males (alate) and sexual forms have bamates and pyrethroids (CABI data base, been recorded in Germany (Falk, 1960). Tem- 2016). However, decisions concerning the peratures that range between 24 and 28.5°C chemical treatment against A. craccivora and 65% relative humidity (= RH) are opti- should take into account the identity and mal conditions for the development of A. abundance of local populations of its natu- craccivora (Réal, 1955; Mayeux, 1984), which ral enemies in the context of an integrated is capable of rapid population development. pest management, so as to avoid outbreaks Formation of winged individuals is triggered of this important pest. by the reduction in the intensity of hydro- carbon translocation (Mayeux, 1984). Young colonies concentrate on growing points of Literature cited plants and are regularly attended by ants (mutualism with ants) (Soans and Soans, Blackman, R.L. and Eastop, V.F. 2000. Aphids on the World’s Crops. An Identifi cation and Informa- 1971; Hamid et al., 1977; Takeda et al., 1982; tion Guide. Second Edition. The Natural Histo- Patro and Behera, 1991). ry Museum, London, 466 pp. The spectrum of natural enemies that Blackman, R.L. and Eastop, V.F. 2007. Taxonom- are associated with A. craccivora is wide. For ic Issues. In: van Emden H.F. and R. Harrington instance, Kavallieratos et al. (2004, 2016) re- (eds.). Aphids as Crop Pests. Wallingford, Oxford- shire, pp 1-30. ported 13 parasitoid species (Hymenoptera: CABI data base. 2016. http://www.cabi.org/isc/ Braconidae: Aphidiinae) that parasitize this datasheet/6192. aphid in agricultural and non-agricultur- Falk, U. 1960. Fber das Auftreten von IntermediSr- al ecosystems in southeastern Europe, i.e., formen zwischen oviparem und gefl ügeltem © Benaki Phytopathological Institute Aphis craccivora on aronia crop in Montenegro 69 viviparem Weibchen bei Aphis craccivora Koch. ent host plants. North-Western Journal of Zoolo- Zoologischer Anzeiger, 165: 388-392. gy, 8(1): 172-180. Hamid, S., Sha, M.A. and Anwar, M.A. 1977. Some Nikolić, M.D. and Milivojević, J.M. 2010. Jagodaste ecological and behavioural studies on Aphis voćke - Tehnologoja gajenja. Naučno voćarsko craccivora Koch (Hemi.: Aphididae). Technical društvo Srbije, Čačak. Bulletin, Commonwealth Institute of Biological Patro, B. and Behera, M.K. 1991. Mutualism between Control, 18: 99-111. the bean aphids (Aphis craccivora Koch) and ants. Hareendranath, V., Nair, K.P.V. and Paulos, S. 1987. Orissa Journal of Agricultural Research, 4: 238. Fusarium pallidoroseum (Cooke) Sacc. as a fun- Réal, P. 1955. Le cycle annuel du puceron de l’arachi- gal pathogen of Aphis craccivora Koch. Ento- de (Aphis leguminosae Theob.) en Afrique noire mon, 12: 392-394. française et son déterminisme. Revue de Patho- Kavallieratos, N.G., Tomanović, Ž, Starý, P., Athanas- logie Végétale et d’Entomologie agricole de Fran- siou, C.G., Sarlis, G.P., Petrović, O., Niketić, M. ce, 34(1-2): 1-122. and Anagnou-Veroniki, M. 2004. A survey of Sewify, G.H. 2000. Neozygites fresenii causing epi- aphid parasitoids (Hymenoptera: Braconidae: zootic in aphids (Aphis craccivora Koch.) popula- Aphidiinae) of southeastern Europe and their tion on faba bean in Egypt. Bulletin of Faculty of aphid - plant associations. Applied Entomology Agriculture, University of Cairo, 51: 85-94. and Zoology, 39: 527-563. Soans, A.B. and Soans, J.S. 1971. Proximity of the col- Kavallieratos, N.G., Tomanović, Ž., Sarlis, G.P, Vayias, onies of the tending ant species as a factor de- B.J., Žikić, V. and Emmanouel, N.E. 2007. Aphids termining the occurrence of aphids. Journal of (Hemiptera: Aphidoidea) on cultivated and self- the Bombay Natural History Society, 68: 850-851. sown plants