Aphid species (Hemiptera: Aphididae) reported for the first time in Tucuman, Argentina.
There have been 336 species of aphids recorded in South America (Ortego pers. comm. 2014) of which 237 are present in Argentina (Nieto Nafria et al. 1994; Ortego et al. 2004; Ortego et al. 2006; Mier Durante et al. 2011; Mier Durante et al. 2012; Ortego et al. 2014). In Tucuman province, located in northwestern Argentina, 64 different species associated with several crops and ornamental plants have been cited (Ovruski de Martinez & Delfino 1990; Nieto Nafria et al. 1994; Ovruski de Martinez et al. 1997). According to Taylor (cited by Cermeli 1987), the species involved in an agro-ecosystem and their densities are highly variable among seasons and locations. For this reason, the aim of this work was to establish if there were aphid species in Tucuman, Argentina, that have not been previously recorded in the Province.
MATERIALS AND METHODS
Aphid sampling were conducted in potato crops, during the 2010 to 2012 seasons, in 3agrological regions of Tucumanprovince that have different geographical and climatic characteristics (Alto Verde: S 27[degrees]21'-W 65[degrees]40' O; Tafi del Valle: S 26[degrees] 54'-W 65[degrees]45'; Las Talitas: S 26[degrees]48'-W 65[degrees] 12'). Every week winged forms of aphids were collected with modified Moericke yellow water pan traps (Moericke 1955). Each pan was made of plastic and was slightly smaller (53 x 35 x 11 cm) than the original. Specimens were preserved in 70% ethanol until identification. Several keys were used to identify the species: Remaudiere & Seco Fernandez (1990); Blackman & Eastop (2000) and Taylor & Robert (1984), although sometimes only the genera could be determined. The Remaudiere, Stroyan & Quednau extended classification (from Nieto Nafria & Colin 2011) is used in this work.
Literature was consulted to determine which of the species collected were cited previously in Argentina and Tucuman Province (Nieto Nafria et al. 1994; Ortego et al. 2004; Ortego et al. 2006; Ovruski de Martinez et al. 1997; Mier Durante et al. 2011; Mier Durante et al. 2012; Ortego et al. 2014). A table was prepared taking into account the following information for each species: Family, subfamily, tribe, valid name, name of author and first report in Argentina. Voucher specimens were slide mounted and deposited in the EEAOC collection.
Forty-seven species among 56 taxa were identified in this work. All of them had already been cited in Argentina in the past, but 17 of them and the genus Illinoia are mentioned for the first time in Tucuman province. All species belonged to the Aphididae family and within it to 4 subfamilies. Aphidinae was the subfamily with the most species, 10 of which belong to the Macrosiphini tribe (Table 1). An annotated list of the species recorded for the first time in Tucuman is given below.
CAPITOPHORUS HIPPOPHAES (WALKER)
This species is recognized among other members of this genus to present swollen siphunculi. In the spring apterae colonize Elaeagnaceae (Elaeagnus spp., Hippophae spp.). They are pale green, slender, with a faint pattern of green spots. Fundatrices are very different; broadly oval, greenish with reddish spots, and their antennae are dark, 5-segmented and have a short processus terminalis. Alatae, produced in the second and third generations, are grayish-green with a black head and thorax, dark antennae, legs and siphunculi and a large quadrate dark green patch on the dorsal abdomen; they migrate to various Polygonum and Persicaria spp. (Hille Ris Lambers 1953). Able to transmit Potato virus Y (PVY) (Van Hoof 1980). Occurs in Europe, North Africa, South-West Asia, and America (USA, Canada, Colombia, Cuba, Mexico, Brazil, Bolivia). In South America, is found in Chile and Argentina (Ortego et al. 2004). In Argentina has been cited in Santa Fe (Ortego et al. 2002), Buenos Aires, Mendoza and Misiones (Ortego et al. 2010).
CHAITOPHORUS LEUCOMELAS KOCH
Apterae are rather elongate oval, pale green or yellow, typically with black or dark green longitudinal pleural stripes that may be segmentally divided, and dark siphunculi. Alatae have dark brown dorsal abdominal cross-bands and separate marginal sclerites. Males can be winged or wingless. The cauda is less pigmented than siphunculi. On young shoots of Populus spp. in spring, and later under leaves; always ant-attended. Common and widely distributed in Europe, Asia, South Africa, North and South America (Chile, Munoz & Beeche 1995 and Argentina). In Argentina was cited in Mendoza (Ortego et al. 1999), Rio Negro and Neuquen (Delfino 2002).
CRYPTOMYZUS (CRYPTOMYZUS) BALLOTAE HILLE RIS LAMBERS
On Ballota nigra, Lamium album, Leonurus sp., Marrubium vulgare and Melittis melissophyllum. In Europe, and possibly Pakistan, where it may be heteroecious holocyclic with a sexual phase on Ribes orientale. Probably anholocyclic in Europe, although oviparae and alate males have been obtained in the laboratory. Able to transmit Potato virus Y(PVY). Mentioned for the first time in Argentina in 1991 in Mendoza (Ortego 1991) on Marrubium vulgare and Lamium amplexicaule and in Chile (Ortego 1998a).
DYSAPHIS (POMAPHIS) AUCUPARIAE (BUCKTON)
Spring generations live on Sorbus torminalis. Migration occurs in the third and subsequent generations to Plantago spp., especially P. lanceolata, where it colonizes the undersides of leaves, in grooves between veins, attended by ants. In Europe, also populations are found on Plantago in Australia (Carver & Hales 1983), New Zealand (Sunde 1984) and Argentina (Ortego 1998a), and alatae have also been trapped in Washington, USA (BMNH collection; leg. S. H. Halbert).
EUCARAZZIA ELEGANS (FERRARI)
Rather small, broadly oval, green aphids feeding on the undersides of leaves, shoots or flowers of Mentha spp. and various other Labiatae. The alatae of E. elegans are easily identifiable by observing the siphunculi, which have a dark swollen extremity and a pale cylindrical base, and their wings, which have dark triangular spots at the ends of all the veins. In the mediterranean area, Madeira, middle East, Central Asia, Pakistan, India, Australia, Africa, western USA and South America (Bolivia, Argentina and Brazil). In Argentina was first cited by Ortego in 1994 on Lavandula sp.
HYADAPHIS FOENICULI (PASSERINI)
Apterae are small to medium size, predominantly grayish-green with dark antennae, legs, siphunculi and cauda; body variably dusted with fine white wax. Alatae have the abdomen green mottled with darker green and with darker patch around the base of each siphunculus. Primary host are Lonicera spp. and secondary hosts are numerous species of Umbelliferae. Vector of about 13 plant viruses, including Celery mosaic potyvirus, Potato virus Y potyvirus, Celery yellow spot luteovirus, and Honeysuckle latentcarlavirus. Almost cosmopolitan: Europe, Middle East, southern Africa, India, Australia, New Zealand and North and South America. In Argentina was cited in Buenos Aires, San Juan, Cordoba (Nieto Nafria et al. 1994) and Mendoza (Ortego 1998a).
About 45 North American species and one from the Caucasus. Illinoia are pale spindle-shaped aphids with long appendages, most easily recognized by the long weakly to moderately clavate siphunculi, similar to those of Amphorophora, but ornamented on the distal, constricted region with a few rows of polygonal reticulation. There is no host alternation. In Argentina, the only species cited is Illinoia (Illinoia) azaleae (Mason), recorded for the first time on Rhododendron sp. in Mendoza province (Ortego et al. 2004).
MACROSIPHONIELLA (MACROSIPHONIELLA) ARTEMISIAE (BOYER DE FONSCOLOMBE)
Large, green aphids with fine white wax; head, antennae, legs, siphunculi and cauda dark, without dorsal sclerotization. The siphunculi are wider at the ends than in the middle and the reticulation covers half of its length, which is similar to the cauda. Common on upper parts of Artemisia vulgaris, especially between inflorescences, and frequently forming large colonies. Throughout Europe, Siberia, Mongolia and China, and introduced to North and South America. In Argentina was cited in Buenos Aires, Cordoba, Santa Fe province (Nieto Nafria et al. 1994; Ortego et al. 2002) and Mendoza (Ortego 1998a).
MACROSIPHONIELLA (MACROSIPHONIELLA) TAPUSKAE (HOTTES & FRISON)
Apterae are pale green, with a darker green spot on abdominal tergite 5 between the siphuncular bases. On various Anthemidae (Achillea, Anacyclus, Anthemi, Argyranthemum, Artemisia, Chrysanthemum, Matricaria, Tanacetum), usually feeding on lower leaves. Europe, Russia, Asia, North Africa and North America, and more recently recorded from Argentina (Ortego et al. 2006).
PLEOTRICHOPHORUS GLANDULOSUS (KALTENBACH)
Apterae are yellowish white, sometimes greenish, occasionally with pale green median stripes. On undersides of lower leaves of Artemisia vulgaris, and sometimes on other Artemisia spp. In Europe and across Asia and introduced to North America. Also, was found in Mendoza, Argentinaon A. verlotorum and A. absinthium (Ortego 1991, 1998a) and Uruguay (BMNH collection, leg. V. F. Eastop).
RHOPALOMYZUS POAE (GILLETTE)
Apterae are small, broadly pear-shaped, pale to dark-brown or almost black, shiny and with a bluish waxy bloom. Alatae have extensive black dorsal abdominal pigmentation. This species lives on the basal parts of grasses close to soil level and often on etiolated stems under stones. Is recorded as vector of Barley yellow dwarf luteovirus and Maize dwarf mosaic potyvirus (Blackman & Eastop 2000). Widely distributed in Europe and the USA. There are also records from Argentina (Ortego 1991), Pakistan, Bolivia and Peru.
SALTUSAPHIS SCIRPUS THEOBALD
Apterae are greyish yellow to greenish yellow, with dark markings tending to form longitudinal bands, the dorsum being powdered with a very thin layer of greyish white wax. Alatae have broad dark dorsal abdominal cross bars and dark-bordered wing veins with spots at their apices, and antennae with 10-21 rhinaria on III. On various Cyperaceae (Carex, Cyperus, Scirpus). In Europe (not UK), across Asia and Africa. Also now in Argentina, recorded in Mendoza (Ortego et al. 2006) and Cordoba (Ortego, data not published).
SIPHA (RUNGSIA) MAYDIS PASSERINI
Apterae are rather small, pear-shaped dorsoventrally flattened, shining dark brown to almost black on dorsal surface, which is fully sclerotized. Usually live on upper sides of leaf blades near the bases and sometimes on stems or flower heads, of grasses and cereals, often attended by ants. Alatae have a solid black patch extending over abdominal tergites 4-7, with separate dark transverse bands on tergites 1-3. Recorded only from Gramineae, in all the economically important cereal crops. Able to transmit Cucumber mosaic cucumovirusand Barley yellow dwarf luteovirus (Blackman & Eastop 2000). Present in Europe, the mediterranean, the middle East, Central Asia, India, Pakistan and South Africa. In North America was recently found (Sorensen 2007; Halbert et al. 2013). In Argentina was recorded in 2002 (Delfino 2002; Ortego & Difabio 2002).
TAKECALLIS ARUNDINARIAE (ESSIG)
Alatae are whitish, pale yellow or greyish-yellow, with paired black elongate spots on abdominal tergite 1-7 and a pale cauda. An apterous morph has been described, but only from high altitudes in Taiwan. On undersides of mature leaves of bamboos (especially Arundinaria and Phyllostachys, but sometimes also Bambusa, Dendrocalamus, Pseudosasa and Sasa). In India, China, Taiwan, Korea, Japan and introduced to England, madeira (Aguiar & Ilharco 1997), Australia (Valenzuela et al. 2010), New Zealand, North and South America (Chile and Argentina). In Argentina was cited in Cordoba (Delfino 2001), mendoza and Buenos Aires (Ortego et al. 2004).
TAKECALLIS TAIWANUS (TAKAHASHI)
Alatae are pale green with a pale cauda. On young, still unrolled leaves and on new shoots of bamboos (Arundinaria and Phyllostachys, sometimes Bambusa, Sasa). In China, Taiwan, Japan and introduced to Europe, South Africa, New Zealand, USA, and more recently to South America (Chile and Argentina). In Argentina was registered for the first time in 2001 (Delfino 2001) and then in mendoza (Ortego et al. 2004).
THERIOAPHIS (RHIZOBERLESIA) RIEHMI (BORNER)
Apterae do not occur; alatae are yellowish, with 2 rows of large dark dorsal spots. On undersides of leaves of Melilotus spp., the preferred hosts, causing yellow sectors in the leaves. There are also records from species of Medicago, Trigonella and Trifolium. In Europe, middle East, India, China, introduced to North and South America (Blackman & Eastop 2000). In Argentina, it has been previously cited in mendoza, San Juan and Cordoba province (Ortego 2000). monoecious holocyclic with oviparae and alate males in September (Hille Ris Lambers & Van den Bosch 1964).
TUBERCULATUS (TUBERCULATUS) QUERCEUS (KALTENBACH)
The alatae forms are dirty greenish to straw-colored, covered with fine powdery white wax, with a dark bifurcate spinal process have only one pair of large, black, spinal tubercles in the first segment of the abdomen. A dark patch near end of hind femur and dark siphunculi. There are no records of their capacity of virus transmission (Blackman &Eastop 2000). On undersides of leaves of Quercus robur in Europe, Iran, Turkey and the Caucasus (Heie 1982), and introduced to British Columbia, Canada (Blackman & Eastop 2000), and to South America (Argentina and Chile, Caballero et al. 2000, Nieto Nafria et al. 1994; Ortego et al. 2006).
TUBERCULATUS (TUBERCULOIDES) ANNULATUS (HARTIG)
Alatae (only oviparae are apterous) have 3 pairs of spinal tubercles lightly pigmented or pale on anterior abdominal segments. Yellowish, greyish-green or pink to purple in summer, with black-banded antennae, black tarsi, and dark distal two thirds or more of siphunculi. On undersides of leaves of Quercus spp., especially Q. robur, less commonly Q. petraea. There are no records of their capacity of virus transmission. Present in all continents (Blackman & Eastop 2000). Throughout Europe, Siberia (Pashchenko 1988b), north-west China (Qiao et al. 2005). In North America, Canada and USA and introduced on European oaks to Australia, New Zealand, North and South America (Chile and Argentina). In Argentina, it was found in Buenos Aires, Cordoba, Corrientes, Entre Rios, Mendoza and Santa Fe (Nieto Nafria et al. 1994).
Results indicate that the geographic distributions of aphid taxa are unrelentingly expanding and therefore faunistic studies should be conducted without interruption in areas of interest. This research updates previous surveys and provides new data, both in terms of locations and species diversity. As other authors have previously proposed (Remaudiere et al. 1992; Nieto Nafria et al. 1994; Ortego 1998b; Ortego et al. 2002), it is necessary to intensify the aphid studies in Argentina. This study, conducted only in fields of potato, was sufficient to find 17 species and a genus that had not been previously cited in our province. Given the importance of aphids as agricultural pests and virus vectors, it is highly recommended to enhance species diversity surveys in Tucuman and other provinces of Argentina. Such taxonomic and ecological information is essential for developing strategies to manage aphid pest and aphid transmitted pathogens of various crops.
We thank Dra. Gabriela Murua, Ing. Agr. Ramiro Lobo and Ing. Agr. Alicia Forns for their excellent technical support.Also, thanks to Ing. Agr. Gerardo Gastaminzafor his critical review, and to the reviewers for their comments and important contributions to the manuscript. This study was supported by EEAOC and CONICET and it is part of the first author's doctoral thesis.
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A. L. Avila (1,2), *, M. A. Vera (1), J. Ortego (3), e. Willink (1), L. D. Ploper (1,2) and V. C. Conci (4)
(1) Estacion Experimental Agroindustrial Obispo Colombres (EEAOC), Seccion Zoologia Agricola. Las Talitas (T4104AUD), Tucuman, Argentina
(2) Instituto de Tecnologia Agroindustrial del Noroeste Argentino (ITANOA-EEAOC) Consejo Nacional de Investigaciones Cientificas y Tecnicas (CONICET)
(3) Instituto Nacional de Tecnologia Agropecuaria (INTA), EEA Mendoza, Argentina
(4) IPAVE, Instituto de Patologia Vegetal--CIAP-INTA (CONICET), Cordoba, Argentina
Corresponding author; E-mail: firstname.lastname@example.org
TABLE 1. APHID SPECIES OF THE FAMILY APHIDIDAE NOT PREVIOUSLY RECORDED IN TUCUMAN PROVINCE, ARGENTINA. THESE SPECIES ALSO OCCUR ELSEWHERE IN ARGENTINA. Subfamily Tribe Species Chaitophorinae Chaitophorini Chaitophorus leucomelas Koch Siphini Sipha maydis Passerini Calaphidinae Panaphidini Takecallis arundinariae (Essig) Takecallis taiwanus (Takahashi) Therioaphis riehmi (Bonier) Tuberculatus annulatus (Hartig) Tuberculatus querceus (Kaltenbach) Saltusaphidinae Macro siphini Saltusaphis scirpus Theobald Aphidinae Capitophorus hippophaes (Walker) Ciyptomyzus ballotae Hille Lis Lambers Dysaphis aueupariae (Buckton) Eucarazzia elegans (Ferrari) Hyadaphis foenieuli (Passerini) Illinoia sp.Wilson Macrosiphoniella artemisiae (Boyer de Fonscolombe) Macrosiphoniella tapuskae (Hottes & Frison) Pleotrichophorus glandulosus (Kaltenbach) Rhopalomyzus poae (Gillette) Subfamily Tribe First report in Argentina Chaitophorinae Chaitophorini Ortego et al. 1999 Siphini Deitino 2002; Urtego & Difabio 2002 Calaphidinae Panaphidini Delfino 2001 Delfino 2001 Ortego 2000 Blanchard 1926 Smith & Cermeli 1979 Saltusaphidinae Macro siphini Ortego et al. 2006 Aphidinae Ortego 1991 Ortego 1991 Ortego 1998a Ortego 1994 Blanchard 1935 Ortego et al. 2004 Nieto Nafria et al. 1994 Ortego et al. 2006 Ortego 1991 Ortego 1998b
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|Author:||Avila, A.L.; Vera, M.A.; Ortego, J.; Willink, E.; Ploper, L.D.; Conci, V.C.|
|Date:||Dec 1, 2014|
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