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Revista Brasileira de Entomologia

Print version ISSN 0085-5626On-line version ISSN 1806-9665

Rev. Bras. entomol. vol.63 no.2 São Paulo Apr./June 2019  Epub June 13, 2019

https://doi.org/10.1016/j.rbe.2019.02.007 

Short Communications

First record of the sedge feeder Bactra verutana Zeller (Lepidoptera: Tortricidae) in Chile based on morphology and DNA barcodes

Héctor A. Vargasa  * 

Marcelo Vargas-Ortizb 

aUniversidad de Tarapacá, Facultad de Ciencias Agronómicas, Departamento de Recursos Ambientales, Arica, Chile

bUniversidad de Concepción, Facultad de Ciencias Naturales y Oceanográficas, Departamento de Zoología, Programa de Doctorado en Sistemática y Biodiversidad Concepción, Chile


Abstract

The sedge-feeding moth Bactra verutana Zeller, 1875 (Lepidoptera: Tortricidae: Olethreutinae: Bactrini), described from Dallas, Texas, USA, is widespread, recorded throughout much North America, Central and South America, including the Caribbean, and Africa. The species is recorded for the first time from Chile based on specimens collected in the coastal valleys of the Atacama Desert, where its larvae feed on Cyperus corymbosus Rottb. var. subnodosus (Nees & Meyen) Kük. (Cyperaceae). A single DNA barcode haplotype, which is widespread in USA, was found in two Chilean specimens sequenced.

Keywords Atacama Desert; Cyperaceae; Cyperus corymbosus; DNA barcoding

Bactra Stephens, 1834 (Olethreutinae: Bactrini) is a widespread genus of Tortricidae (Lepidoptera) with 106 described species worldwide (Gilligan et al., 2014), 13 of which are recorded in the Neotropical Region (Razowski and Becker, 2010). Host plant records, available for 21 species, are mainly restricted to representatives of Cyperaceae, Juncaceae and Poacae, upon which the larvae feed on stems (Horak, 2006; Brown et al., 2008). In contrast to the general habit of feeding on monocotyledenous hosts, the Palearctic Bactra bactrana (Kennel, 1901) was recently recorded as a pest of sweet pepper Capsicum annuum L. (Solanaceae) (Roditakis et al., 2016).

Bactra verutana Zeller, 1875 is one of the species in the genus whose biology has been best studied. It has been proposed as a biological control agent of weed sedges, because its larvae are voracious stem borers on these plants (Keeley et al., 1970; Frick and Garcia, 1975; Frick and Wilson, 1978). Originally described from Dallas, Texas, USA, it is currently widespread in the New World, with records from much of North America and several localities in Central and South America, the Caribbean Islands and Africa (Diakonoff, 1964; Powell, 1997; Razowski and Becker, 2010).

We provide the first record of B. verutana from Chile based on sampling conducted in the northernmost part of this country. Because the genitalia of some representatives of Bactra are morphologically similar (e.g.: Diakonoff, 1963, 1964), DNA barcode sequences (sensu Hebert et al., 2003) were used to assess the relationships of the Chilean specimens.

Sampling. Adults were collected at light in the Azapa Valley, Atacama Desert of northern Chile, between July 2015 and January 2018. Larvae were collected on the sedge Cyperus corymbosus Rottb. var. subnodosus (Nees & Meyen) Kük. (Cyperaceae) in the same locality. Stems bored by larvae were placed in plastic vials with paper towel at the bottom; additional pieces of stems were provided when needed. Plastic vials were periodically checked for adult emergence. Two larvae were placed in 95% ethanol at −20 °C until DNA extraction. The abdomens of adults were dissected using hot 10% KOH for a few minutes; the genitalia were stained with Chlorazol Black or Eosin Y and slide mounted with Euparal. Vouchers are deposited in IDEA (Colección Entomológica, Universidad de Tarapacá, Arica, Chile).

DNA extraction and analysis. DNA extraction followed the procedures described in Huanca-Mamani et al. (2015). Genomic DNA was sent to Macrogen (South Korea) for amplification, purification and sequencing of the barcode region using the primers LCO-1490 and HCO-2198 (Folmer et al., 1994) following the amplification program described in Escobar-Suárez et al. (2017). For phylogenetic analysis, additional DNA barcode sequences (658 bp; Table 1) were downloaded from BOLD (Ratnasingham and Hebert, 2007): one of each haplotype of B. verutana and one of each other species of Bactra, except for B. blepharopis Meyrick, 1911, in which the two available haplotypes were included, as this species showed the lowest K2P distance with B. verutana. A sequence of Endothenia Stephens, 1852 (Endotheniini) was also included in the analysis as a representative of the sister tribe of Bactrini (Regier et al., 2012). The sequences were aligned by the ClustalW method, and sequence divergence was estimated by the Kimura 2-parameter model (K2P) in the software MEGA6 (Tamura et al., 2013) using 1000 bootstrap replications. Coalescent trees were inferred using the Bayesian method through BEAST 1.8.4 (Drummond et al., 2012) based on a Yule species tree prior. The nucleotide substitution model JC was the most appropriate according to the Bayesian information criterion obtained in JModelTest 2.1 (Darriba et al., 2012). A Markov Chain Monte Carlo (MCMC) process was run for 10 million generations, sampling every 1000 generations. We used MCMC sampling with priors above 200 to ensure effective sample sizes, which were assessed in Tracer 1.6 (Rambaut et al., 2014). Ten percent of the samples were removed as “burn-in” in TreeAnnotator 1.8.4 (http://beast.community/treeannotator). Finally, the consensus tree obtained was viewed and edited in FigTree 1.4.3 (http://tree.bio.ed.ac.uk/software/figtree).

Table 1 Sequences used in the Bayesian analysis. 

Species BOLD accession GenBank
accession
Country
Bactra ablabes Turner,
1946
ANICV1650-11 KF404098.1 Australia
Bactra blepharopis
Meyrick, 1911
ANICC250-09 Australia
Bactra blepharopis
Meyrick, 1911
MAMOT3760-
13
KX862772.1 Pakistan
Bactra furfurana
(Haworth, 1811)
BBLOD1417-11 United States
Bactra lacteana Caradja,
1916
DEEUR370-12 Germany
Bactra maiorina
Heinrich, 1923
LOCB575-06 United States
Bactra optanias
Meyrick, 1911
ANICB519-06 Australia
Bactra passercula
Turner, 1916
ANICV1671-11 KF402375 Australia
Bactra priapeia
Heinrich, 1923
LMEMB250-09 United States
Bactra robustana
Christoph, 1872
CGUKC306-09 United Kingdom
Bactra scalopias
Meyrick, 1911
ANICV1656-11 KF404800.1 Australia
Bactra suedana
Bengtsson, 1989
LEEUA224-11 Denmark
Bactra venosana (Zeller,
1847)
ANICB611-06 Australia
Bactra verutana Zeller,
1875
BBLOE331-11 United States
Bactra verutana Zeller,
1875
BBLOE1159-12 United States
Bactra verutana Zeller,
1875
BBLOB1839-11 United States
Bactra verutana Zeller,
1875”
BLPDG174-09 Costa Rica
Bactra verutana Zeller,
1875”
BLPDH685-09 Costa Rica
Bactra verutana Zeller,
1875
LMEMB244-09 United States
Bactra verutana Zeller,
1875”
MIMAD026-15 Madagascar
Bactra verutana Zeller,
1875”
MIMAD662-15 Madagascar
Bactra verutana Zeller,
1875
MH938331 Chile
Endothenia
gentianaeana (Hubner,
[1796-1799])
CGUKC916-09 United Kingdom

Morphology. Eight adults (four females, four males), two of which were reared from larvae collected on C. corymbosus, were dissected and identified as B. verutana based on genitalia morphology (Diakonoff, 1964; Powell, 1997) (Fig. 1).

Fig. 1 Adult Bactra verutana collected in the Azapa Valley, northern Chile. (A) Male in dorsal view. (B) Female genitalia in ventral view. (C) Male genitalia in ventral view. Scale bars 1, 0.2 and 2.2 mm, respectively. 

DNA barcodes and phylogenetic analysis. Two DNA barcode sequences (658 bp), representing a single haplotype (GenBank accession MH938331), were obtained from the borer larvae collected on stems of C. corymbosus. A search in BOLD revealed that this haplotype is widespread in the USA (Alabama, Arizona, Arkansas, Florida, Illinois, Maryland, Massachusetts, Mississippi, Oklahoma, Tennessee and Texas). Pairwise distances (K2P) of the Chilean haplotype were 0-0.3%, 2.0-2.2% and 6.0-6.2% with those of B. verutana from USA, Madagascar and Costa Rica, respectively. Agreeing with this deep divergence, the phylogenetic analysis showed that the B. verutana haplotypes are not monophyletic; the Chilean haplotype clustered with high support only with those from the USA (Fig. 2). This USA-Chile group was sister to B. blepharopis. The haplotypes from Costa Rica and Madagascar were clustered with high support according to geographic origin in two distantly related groups. Those from Costa Rica were clustered with Bactra ablabes Turner, 1946 and those from Madagascar were sister to the group (B. verutana USA-Chile + B. blepharopis). Pairwise distances of the Chilean haplotype with other representatives of Bactra ranged from 1.7 (B. beplarophis) to 8.6% (B. scalopias Meyrick, 1911).

Fig. 2 Bayesian tree of Bactra verutana and congenerics based on sequences of the DNA barcode fragment (658 bp) of the cytochrome c oxidase subunit I (COI) gene. Node supports (posterior probability) indicated above branches. 

Remarks. The Tortricidae of Chile were revised by Razowski and Pelz (2010), providing a valuable base for a wide range of studies, including taxonomic ones. Recent field surveys have revealed previously unknown endemic representatives of this micromoth family in this country (e.g.: Cepeda, 2017; Urra, 2017), suggesting that the diversity of this fauna remains insufficiently described. Based on the available data, the Tortricidae of South and Central Chile are characterized by a high level of endemism (Razowski and Pelz, 2010; Cepeda, 2017; Urra, 2017), whereas less endemism is found in the arid environments of the northernmost part of the country (Brito and Vargas, 2018; Vargas-Ortiz and Vargas, 2018). Finding B. verutana in the coastal valleys of the Atacama Desert provides an additional record of a widespread, non-endemic tortricid moth for northern Chile.

The habit of feeding on sedges as a stem borer has been well described previously for B. verutana (Keeley et al., 1970; Frick and Garcia, 1975; Frick and Wilson, 1978), with at least three species of Cyperus recorded as its hosts, besides unidentified representatives of Scirpus (Cyperaceae) and Juncus (Juncaceae) (Brown et al., 2008). Thus, the record of C. corymbosus here reported for the Chilean specimens agrees with the main association of B. verutana with Cyperaceae. Obviously, the presence of such a suitable host was indispensable for the colonization of the coastal valleys of the Atacama Desert by this specialized sedge-feeding micromoth.

In accordance with the patterns described for other Lepidoptera families (Hebert et al., 2003), intraspecific DNA barcode divergences are in general lower than 2% in Tortricidae (Hulcr et al., 2007; Gilligan et al., 2016; Corley and Ferreira, 2017; Vargas-Ortiz et al., 2017), although cases of greater divergence have been described for a few widespread species (Gilligan et al., 2016). The deep divergence of the BOLD sequences of B. verutana and the results of the phylogenetic analysis, in which the haplotypes from Madagascar and Costa Rica were not clustered with those from USA, strongly suggest that more than one species is present under this name in this database. It is supposed that the haplotypes from North America represent the true B. verutana, as this group includes sequences sampled close to the type locality (Texas, USA). The divergence between the North American haplotypes of B. verutana and the two haplotypes of B. blepharopis (1.7-2.0%) is close to the highest values of intraspecific divergence reported for a few widespread tortricids (Gilligan et al., 2016); however, the two are currently considered valid species based on morphology (Horak, 2006; Gilligan et al., 2014). In addition, the reciprocal monophyly found in the phylogenetic analysis between the North American haplotypes of B. verutana and those of B. blepharopis reinforces their heterospecific status.

The low divergence and the grouping of the only Chilean haplotype with the North American ones in the phylogenetic analysis provides additional support for the morphological identification of B. verutana in Chile. These results also suggest a recent arrival of this species to the Atacama Desert; however, understanding the phylogeographic patterns throughout its remarkably wide New World range deserves further molecular studies. Meanwhile, the taxonomic status of the populations from Costa Rica and Madagascar should be assessed using integrative approaches.

Acknowledgements

We thank two anonymous reviewers for kind comments and suggestions on a preliminary version of the manuscript, Wilson Huanca-Mamani for providing support for DNA extractions and Lafayette Eaton for checking the English. The study was supported by project UTA-MAYOR 9722-18 from Universidad de Tarapacá and project EDPG LPR-161 of Dirección de Postgrado from Universidad de Concepción.

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Received: October 4, 2018; Accepted: February 27, 2019

* Corresponding author. E-mail:havargas@uta.clE-mails:lepvargas@gmail.com (H.A. Vargas).

Conflicts of interest

The authors declare no conflicts of interest.

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