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First high-altitude record of Bucculatrix mirnae Vargas and Moreira (Lepidoptera, Bucculatricidae) on a newly documented host plant: the importance of host plant distribution for conservation on the western slopes of the Andes mountains of northern Chile

ABSTRACT

Bucculatrix mirnae Vargas and Moreira, 2012 (Lepidoptera, Bucculatricidae) is a micromoth native to the coastal valleys of the Atacama Desert previously known to occur only in the type locality of the Azapa Valley, close to sea level. Its immature stages are associated with the shrub Baccharis salicifolia (Ruiz & Pav.) Pers. (Asteraceae). We report data on the occurrence of B. mirnae found for the first time at 3500 m above sea level on the western slopes of the Andes mountains of northern Chile. In addition, Baccharis alnifolia Meyen & Walp. is recorded as a new host plant for B. mirnae. The implications of this finding for conservation in the arid western slopes of the Andes habitats in northern Chile are discussed.

Keywords:
Asteraceae; Baccharis alnifolia; Baccharis salicifolia; Leaf miner; Leaf skeletonizer

Mountain ecosystems typically harbor a wide range of habitats distributed across altitudinal gradients, along which several parameters related to insect populations and communities can be strikingly affected (Brehm and Fiedler, 2003Brehm, G., Fiedler, K., 2003. Faunal composition of geometrid moths changes with altitude in an Andean montane rain forest. J. Biogeogr. 30, 431-440., Pyrcz et al., 2009Pyrcz, T.W., Wojtusiak, J., Garlacz, R., 2009. Diversity and distribution patterns of Pronophilina butterflies (Lepidoptera: Nymphalidae: Satyrinae) along an altitu- dinal transect in North-Western Ecuador. Neotrop. Entomol. 38, 716-726., Choi and An, 2010Choi, S.-W., An, J.-S., 2010. Altitudinal distribution of moths (Lepidoptera) in Mt. Jirisan National Park. South Korea. Eur. J. Entomol. 107, 229-245., Pellissier et al., 2012Pellissier, L., Fiedler, K., Ndribe, C., Dubuis, A., Pradervand, J.-N., Guisan, A., Rasmann, S., 2012. Shifts in species richness, herbivore specialization, and plant resistance along elevation gradients. Ecol. Evol. 2, 1818-1825., Carneiro et al., 2014Carneiro, E., Mielke, O.H.H., Casagrande, M.M., Fiedler, K., 2014. Skipper richness (Hesperiidae) along elevational gradients in Brazilian Atlantic Forest. Neotrop. Entomol. 43, 27-38., de Groot and Kogoj, 2015de Groot, M., Kogoj, M., 2015. Temperature, leaf cover density and solar radiation influence the abundance of an oligophagous insect herbivore at the southern edge of its range. J. Insect. Conserv. 19, 891-899. and Gillette et al., 2015Gillette, P.N., Ennis, K.K., Martínez, G.D., Philpott, S.M., 2015. Changes in species richness, abundance, and composition of arboreal twig-nesting ants along an elevational gradient in coffee landscapes. Biotropica 47, 712-722.). Thus, descriptive studies on the biodiversity of little-known mountain ecosystems are essential to improve the understanding of ecological and evolutionary aspects of such biota, making it possible to implement better planning and conservation management (Costa et al., 2015Costa, D.P., Santos, N.D., Rezende, M.A., Buck, W.R., Schäfer-Verwimp, A., 2015. Bry- oflora of the Itatiaia National Park along an elevation gradient: diversity and conservation. Biodivers. Conserv. 24, 2199-2212.).

The Andes mountains of northern Chile are characterized by the presence of several vegetation belts, restricted to specific altitudinal ranges, whose biota have been only partially studied (Luebert and Pliscoff, 2006Luebert, F., Pliscoff, P., 2006. Sinopsis bioclimática y vegetacional de Chile. Editorial Universitaria, Santiago, Chile.). Within the Lepidoptera found in this area, butterflies have been relatively well inventoried and investigated in relation to their ecology and conservation status (Despland et al., 2012Despland, E., Humire, R., San Martin, S., 2012. Species richness and phenology of but- terflies along an altitude gradient in the desert of northern Chile. Arct. Antarct. Alp. Res. 44, 423-431., Vargas and Benítez, 2013Vargas, H.A., Benítez, H.A., 2013. Egg phenology of a host -specialist butterfly in the western slopes of the northern Chilean Andes. Neotrop. Entomol. 42, 595-599., Despland, 2014 and Vargas et al., 2015). On the other hand, micromoths have received little attention in the scientific literature, probably due to their inconspicuousness, which has resulted in a very limited sampling effort. Accordingly, the taxonomic composition of the micromoth families remains unknown for the different high-altitude arid habitats of this part of the Andes.

Bucculatricidae is a widely distributed family of micromoths with approximately 250 species described around the world, most of which are represented in the Nearctic region (Braun, 1963Braun, A.F., 1963. The genus Bucculatrix in North America north of Mexico. Mem. Am. Entomol. Soc. 18, 1-208.). Contrastingly, the Neotropical fauna of this family has not yet been comprehensibly studied, as just a few species are recorded in this region (Davis and Miller, 1984Davis, D.R., Miller, S.E., 1984. Lyonetiidae. In: Heppner, J.B. (Ed.), Atlas of Neotrop- ical Lepidoptera, Checklist: Part 1, Micropterigoidea - Immoidea. Dr. W. Junk Publishers, The Hague, p. 25. and Davis et al., 2002).

Larvae of Bucculatricidae are characterized by hypermetamorphic development with up to three morphs in the ontogeny (Friend, 1927Friend, R.B., 1927. The biology of the birch leaf skeletonizer Bucculatrix canaden- sisella. Chambers. Conn. AES Bull. 288, 393-486. and Vargas and Moreira, 2012Vargas, H.A., Moreira, G.R.P., 2012. A new species of Bucculatrix Zeller (Lepidoptera: Bucculatricidae) associated with Baccharis salicifolia (Asteraceae) in northern Chile. Zootaxa 3300, 20-33.). Most species are leaf miners in their early instars, becoming either skeletonizers or stem borers in later instars (Davis and Robinson, 1998Davis, D.R., Robinson, G.S., 1998. The Tineoidea and Gracillarioidea. In: Kristensen, N.P. (Ed.), Handbook of Zoology, Lepidoptera, Moths and Butterflies, vol. 1: Evo- lution, Systematics and Biogeography. Walter de Gruyter, Berlin & New York, pp. 91-117.). On the other hand, there are a number of species that are exclusively leaf miners or gall inducers throughout their lifetime (Braun, 1963Braun, A.F., 1963. The genus Bucculatrix in North America north of Mexico. Mem. Am. Entomol. Soc. 18, 1-208.). Interestingly, in such species whose larvae become external feeders, a smooth molting cocoon is constructed by third and fourth instars, which makes them strikingly different from the conspicuously ridged pupal cocoon constructed by the fifth (last) instar (Braun, 1963).

Bucculatrix mirnaeVargas and Moreira, 2012Vargas, H.A., Moreira, G.R.P., 2012. A new species of Bucculatrix Zeller (Lepidoptera: Bucculatricidae) associated with Baccharis salicifolia (Asteraceae) in northern Chile. Zootaxa 3300, 20-33. is the only species of Bucculatricidae from Chile that has been described to date. Its larvae are associated with Baccharis salicifolia (Ruiz & Pav.) Pers. (Asteraceae), feeding internally as leaf miners during the first three instars, and subsequently changing to external feeding as leaf skeletonizers in the fourth and fifth instars ( Vargas and Moreira, 2012). Although the geographic range of B. mirnae could include additional coastal valleys of the Atacama Desert, records are currently restricted to the type locality of the Azapa Valley ( Fig. 1), in the Arica Province, in northern Chile. The objective of this contribution is to expand the altitudinal range of B. mirnae, to report a new host plant association, and to discuss the importance of host plant distribution to conserve B. mirnae.

Figs. 1-2
The habitats of Bucculatrix mirnae in the arid northern Chile. (1) The lowland Azapa Valley (type locality) located in the coastal Atacama Desert close sea level. (2) The highland neighborhood of Putre village at about 3500 m elevation on the western slopes of the Andes.

As part of a study of the Lepidoptera associated with the native vegetation of northern Chile, nine skeletonizer larvae of Bucculatricidae were found actively feeding on leaves of Baccharis alnifolia Meyen & Walp. (Asteraceae) in July 2013 near Putre village ( Fig. 2), in Parinacota Province, at about 3500 m above sea level. The larvae were collected and brought to the laboratory in plastic vials. Leaves of the same plant were added daily until the last instar started to construct the pupal cocoon. Vials were periodically examined to verify adult emergence. The adults obtained were mounted and studied, following standard procedures for taxonomic identification (Basilio et al., 2015Basilio, D.S., Casagrande, M.M., Bordignon, S.A.L., Moreira, G.R.P., 2015. Descrip- tion and life history of a new cecidogenous species of Palaeomystella Fletcher (Lepidoptera. Momphidae) from Brazil. Rev. Bras. Entomol. 59, 188-196.). Voucher specimens were deposited in the "Colección Entomológica de la Universidad de Tarapacá" (IDEA), Arica, Chile.

Four male and five female adults of B. mirnae were obtained from the larvae collected in the field. This finding expands the altitudinal range of this micromoth by more than 3000 m since it has previously been recorded only at near sea level. In addition, this is the first record of B. alnifolia as a host plant for B. mirnae, as the previous record was on the species B. salicifolia ( Vargas and Moreira, 2012Vargas, H.A., Moreira, G.R.P., 2012. A new species of Bucculatrix Zeller (Lepidoptera: Bucculatricidae) associated with Baccharis salicifolia (Asteraceae) in northern Chile. Zootaxa 3300, 20-33.).

Although several Asteraceae-feeding Bucculatrix have been reared from just one host plant, some species are associated with a few congeneric hosts or with a few hosts belonging to different genera ( Braun, 1963Braun, A.F., 1963. The genus Bucculatrix in North America north of Mexico. Mem. Am. Entomol. Soc. 18, 1-208.). Based on the findings reported here, it seems that the capacity of B. mirnae to use different plants of Baccharis would allow it to survive in both lowland and highland habitats. However, it is known that depending on their dispersal abilities, insect populations can undergo local adaptations and genetic differentiation associated with habitat diversity along altitudinal gradients ( Hodkinson, 2005Hodkinson, I.D., 2005. Terrestrial insects along elevation gradients: species and com- munity responses to altitude. Biol. Rev. 80, 489-513.). For instance, cryptic differentiation correlated with elevation was reported for an endemic micromoth from the Galapagos Islands, clearly associated with different habitats (Schmitz et al., 2008Schmitz, P., Cibois, A., Landry, B., 2008. Cryptic differentiation in the endemic micro- moth Galagete darwini (Lepidoptera. Autostichidae) on Galápagos volcanoes. Philos. Trans. R. Soc. B 363, 3453-3458.). In addition, differential host plant use can play an extremely important role in the ecology and evolution of Lepidoptera ( Ohshima, 2008Ohshima, I., 2008. Host race formation in the leaf -mining moth Acrocercops transecta (Lepidoptera: Gracillariidae). Biol. J. Linn. Soc. 93, 135-145., Jorge et al., 2011Jorge, L.R., Cordeiro-Estrela, P., Klaczko, L.B., Moreira, G.R.P., Freitas, A.V.L., 2011. Host -plant dependent wing phenotypic variation in the neotropical butterfly Heliconius erato. Biol. J. Linn. Soc. 102, 765-774. and Benítez et al., 2015Benítez, H.A., Vargas, H.A., Püschel, T.A., 2015. Left -right asymmetry and morpholog- ical consequences of a host shift in the oligophagous Neotropical moth Macaria mirthae (Lepidoptera: Geometridae). J. Insect Conserv. 19, 589-598.), and cryptic species of micromoths can be associated with different host plants ( Huemer et al., 2014Huemer, P., Karsholt, O., Mutanen, M., 2014. DNA barcoding as a screening tool for cryptic diversity: an example from Caryocolum, with description of a new species (Lepidoptera, Gelechiidae). ZooKeys 404, 91-111. and Kawakita and Kato, 2016Kawakita, A., Kato, M., 2016. Revision of the Japanese species of Epicephala Meyrick with descriptions of seven new species (Lepidoptera. Gracillariidae). ZooKeys 568, 87-118.).

A considerable habitat diversity is represented throughout the altitudinal gradient displayed from the lowland coastal area of the Atacama Desert to the highland Altiplano area of the Andes region in the northernmost part of Chile, where several species of Baccharis are represented ( Luebert and Pliscoff, 2006Luebert, F., Pliscoff, P., 2006. Sinopsis bioclimática y vegetacional de Chile. Editorial Universitaria, Santiago, Chile.). In the case of butterflies, for instance, their distribution and abundance on different altitudinal belts appear to be determined by the presence of adequate host plants ( Benyamini, 1995Benyamini, D., 1995. Synopsis of biological studies of the Chilean Polyommatini (Lepidoptera. Lycaenidae). Rep. Mus. Nat. Hist. Univ. Wisconsin (Stevens Point) 52, 1-51., Despland et al., 2012Despland, E., Humire, R., San Martin, S., 2012. Species richness and phenology of but- terflies along an altitude gradient in the desert of northern Chile. Arct. Antarct. Alp. Res. 44, 423-431., Vargas and Benítez, 2013Vargas, H.A., Benítez, H.A., 2013. Egg phenology of a host -specialist butterfly in the western slopes of the northern Chilean Andes. Neotrop. Entomol. 42, 595-599., Despland, 2014 and Vargas, 2014). Thus, documenting the geographical distribution of the scattered host plants of B. mirnae becomes essential in order to conserve suitable habitats for this micromoth species. Additionally, decision making based upon host plant distribution would allow the conservation of a wide range of high altitude habitats on the western slopes of the Andes mountains of northern Chile, an area with arid habitats under severe threat due to shifts in land use that favor either mining or tourism ( Despland et al., 2012 and Despland, 2014). New species records and associations such as the one presented in this study contribute to reinforce the importance of utilizing new species records to conserve species as well as habitats.

Acknowledgements

The authors thank two anonymous reviewers for suggestions that substantially improved the final version of the manuscript, Dr. Mariana Lazzaro for proof reading this manuscript, and Marcelo Vargas-Ortiz for editing the figures. This study was financed by project grant DGI-UTA9713-16.

References

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  • Benítez, H.A., Vargas, H.A., Püschel, T.A., 2015. Left -right asymmetry and morpholog- ical consequences of a host shift in the oligophagous Neotropical moth Macaria mirthae (Lepidoptera: Geometridae). J. Insect Conserv. 19, 589-598.
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Publication Dates

  • Publication in this collection
    Oct-Dec 2016

History

  • Received
    03 May 2016
  • Accepted
    21 June 2016
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