The Neotropical butterfly Dryas iulia has been collected from several locations in Thailand and Malaysia since 2007, and has been observed breeding in the wild, using introduced Passiflora foetida as a larval host plant. The butterfly is bred by a butterfly house in Phuket, Thailand, for release at weddings and Buddhist ceremonies, and we hypothesized that this butterfly house was the source of wild, Thai individuals. We compared wing patterns and COI barcodes from two, wild Thai populations with individuals obtained from this butterfly house. All Thai individuals resemble the subspecies D. iulia modesta, and barcodes from wild and captive Thai specimens were identical. This unique, Thai barcode was not found in any of the 30 specimens sampled from the wild in the species' native range, but is most similar to specimens from Costa Rica, where many exporting butterfly farms are located. These data implicate the butterfly house as the source of Thailand's wild D. iulia populations, which are currently so widespread that eradication efforts are unlikely to be successful.
Citation: Burg NA, Pradhan A, Gonzalez RM, Morban EZ, Zhen EW, Sakchoowong W, et al. (2014) Inferring the Provenance of an Alien Species with DNA Barcodes: The Neotropical Butterfly Dryas iulia in Thailand. PLoS ONE 9(8): e104076. https://doi.org/10.1371/journal.pone.0104076
Editor: Ben J. Mans, Onderstepoort Veterinary Institute, South Africa
Received: March 30, 2014; Accepted: July 6, 2014; Published: August 13, 2014
Copyright: © 2014 Burg et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Data Availability: The authors confirm that all data underlying the findings are fully available without restriction. All DNA sequences are available from the GenBank database (accession numbers GU157119, GU157122–GU157124, GU157126–GU157131, GU333906, GU333908, GU659588, GU659594, GU659619–GU659626, GU659691, GU666775, GU666782, HM416486, JN201279, JN201280, JQ536893, KJ496350–KJ496367). The DNA sequence alignment is available as Supporting Information.
Funding: National Science Foundation Grant 1120380 to DJL; http://www.nsf.gov/awardsearch/showAward?AWD_ID=1120380. National Science Foundation Grant 0742457 funded NAB; http://www.nsf.gov/awardsearch/showAward?AWD_ID=0742457. Professional Staff Congress of the City University of New York Research Award 60051-40 41 to DJL; https://www.rfcuny.org/rfwebsite/research/content.aspx?catID=1190. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: The authors have declared that no competing interests exist.
The introduction of exotic species to novel habitats is one of the most significant threats to biodiversity conservation. Introduced plants can become invasive, replacing natural vegetation. Introduced predators can consume indigenous prey that lack suitable defenses, and introduced insect herbivores can become plant pests, causing damage to native plants as well as crops . Extensive import laws and quarantine procedures exist in nearly every country to curtail unintentional introduction of pestiferous insects, which could potentially “hitchhike” on imported plants or agricultural produce. Despite the tremendous effort spent trying to prevent the spread of insects between countries, introductions of insect pests are common , .
Once a newly introduced insect has been discovered, it may not possible to determine how the introduction occurred or whether the same species was introduced multiple times. For example, Eastwood and colleagues  used DNA barcodes to demonstrate that all sampled Dominican Papilio demoleus shared a single barcode also found throughout most of Southeast Asia. Since the particular barcode haplotype found in the Dominican Republic is widespread in the Oriental Region, it was not possible to determine the precise location of the source population using DNA barcodes or whether the species was introduced more than once . Determining the provenance of this introduction is important because the Southeast Asian lineage of this species is frequently a pest of Citrus, whereas the lineage from Australia and New Guinea is not , . In addition to assessing the potential crop damage an introduced insect species may cause, knowledge of a species' home range might also be useful for identifying suitable parasitoid species for biological control.
Beginning in 2007, several independent observers recorded specimens of the Julia butterfly, Dryas iulia (Fabricius, 1775), at several locations in Thailand and Malaysia (Fig. 1) including Samui Island (Surat Thani province; Les Day, pers. comm.), Phuket Island (Phuket province; Sin Khoon Khew, pers. comm.), Tioman Island, Malaysia , and Phi Phi Don Island, Thailand (Krabi province; DJL, pers. obs.). Küppers  reported the species from the Thai provinces of Nakhon Si Thammarat, Phang Nga, and Chumphon, and suggested that the species might have escaped from a butterfly house on Phuket.
Orange butterfly symbols indicate localities from which we sampled specimens for this study; black symbols indicate unsampled localities from which the species has been recorded. The image illustrates the wings of specimen DL-08-T033 caught on Phi Phi Don Island, Krabi Province, Thailand.
Dryas iulia is native to the Americas, where thirteen subspecies are found in the southern USA, Central America, the Caribbean, and northern South America , . To identify the Thai specimens to subspecies (Fig. 1), we compared wing patterns of this material to published photographs of all subspecies –. Specimens from Thailand resemble the subspecies Dryas iulia modesta, found in Texas, Mexico, Central America, and the Pacific coast of South America to Ecuador . In their native range, larvae of D. iulia feed on a variety of different Passiflora species (Passifloraceae). Plants in this genus are typically vines or lianas, with more than 100 species in the New World tropics, and about 20 in tropical Southeast Asia, Australia, and New Zealand . The second edition of Butterflies of Thailand  now lists the species as being part of the country's fauna, noting its presence in Chumpon, Nakhon Si Thammarat, and Surat Thani provinces, which are all in the southern peninsula. In Thailand, larvae have been found feeding on Passiflora foetida, and adults frequently nectar on Lantana camara (Les Day, pers. comm.); both of these plants are invasive species native to the Americas , .
The Phuket Butterfly Garden (PBG; 71/6 Moo 5, Soi Paneung, Yaowarat Road, Rassada Rd., Phuket City) has been open since 1990 in the center of Phuket Island, one of the country's most visited tourist areas. In addition to maintaining a butterfly vivarium, the company sells live butterflies for release at weddings (phuketbutterfly.com/wedding.php, accessed March 2014) and provides butterflies for mass public release , . Releasing butterflies at weddings is a relatively new custom practiced around the world. Instead of throwing rice or birdseed at newlyweds as they leave the wedding ceremony, celebrants release live butterflies from an envelope or cage so the couple departs in a swarm of live insects , . After noticing that the PBG website (phuketbutterfly.com, accessed May 2008) showed pictures of D. iulia butterflies, a Thai colleague visited the facility at our request in June 2008. He found D. iulia flying in the vivarium, confirmed with staff that D. iulia could be purchased for release at weddings, confirmed that specimens could be shipped to the resort islands of Samui and Phi Phi Don (where D. iulia has already been observed in the wild), and obtained nine fresh specimens of this species. We subsequently froze the specimens for genetic work.
In the present study, we address two questions: 1) Did wild Thai populations of Dryas iulia originate from livestock at the Phuket Butterfly Garden (PBG)? and 2) From where in its natural range did PBG animals originate? To answer these questions, we sequenced the barcoding section of the mitochondrial cytochrome c oxidase subunit I (COI) gene from wild-caught specimens in Thailand and specimens obtained from PBG. COI evolves rapidly, is easily amplified and sequenced with highly conserved primers, and is therefore a good marker for assessing maternal relatedness and, potentially, species membership . If wild Thai D. iulia were naturalized after introduction from PBG, then DNA barcodes from wild-caught specimens would be similar or identical to barcodes from specimens obtained from PBG. Genetic differences between wild and PBG-derived specimens would suggest that PBG is not the source of Thailand's naturalized D. iulia. However, shared barcode sequences might also result if different populations of the species do not vary at this locus. Therefore, we compared these Thai sequences to barcodes from D. iulia modesta specimens sampled throughout the species' native range, including sequences from GenBank and from D. iulia hispaniola specimens wild-caught in the Dominican Republic. We suspect that PBG stock originated in Costa Rica, as many Neotropical butterfly farms are found here (Michael Boppré, pers. comm.) .
Materials and Methods
Butterfly specimens were caught with an aerial net in the field. Each specimen's wings were removed from its body. Wings were stored in glassine envelopes and bodies were placed in vials of 100% ethanol and frozen. All specimens collected for this study are vouchered in the DNA and Tissues Collection of the Museum of Comparative Zoology, Harvard University (Table 1). Permission to conduct research in Thailand was granted by the National Research Council of Thailand. Permission to export specimens was granted by the CITES Office of the Department of National Parks, Wildlife and Plant Conservation. Permission to conduct research in the Dominican Republic was granted by the Ministerio de Medio Ambiente y Recursos Naturales. Permission to export specimens was granted by the Secretaria de Estado de Agricultura, Departamento de Vida Silvestre, Santo Domingo. All permits in the Dominican Republic were arranged by Kelvin A. Guerrero (kguerrero.net).
Specimens were obtained from colleagues, from the Phuket Butterfly Garden (see Introduction), and from field collection in Thailand and the Dominican Republic. DNA was extracted from single butterfly legs using a QIAGEN DNEasy Blood & Tissue Kit. After addition of the tissue lysis buffer, insect legs were ground mechanically in microcentrifuge tubes using disposable pestles. This step was added to further break down the chitin exoskeleton and thereby maximize the surface area of tissues exposed to the lysis mixture. Subsequently, proteinase-K was added and the manufacturer's protocol was resumed.
A 658 bp fragment of the mitochondrial gene cytochrome c oxidase subunit I (COI) was amplified from whole genomic extracts using the diverse metazoan invertebrate primer pair LCO1490 (5′- TGTAAAACGACGGCCAGTGGTCAACAAATCATAAAGATATTGG-3′) and HCO2198 (5′-CAGGAAACAGCTATGACTAAACTTCAGGGTGACCAAAAAATCA-3′). These primer sequences include the original primers of Folmer et al.  to which M13 tails (indicated in bold) had been concatenated on the 5′ end . Addition of these tails to the primers increases PCR success, particularly on specimens with degraded DNA . PCR products were visualized on agarose gels before being sent to Genewiz (genewiz.com) for PCR clean-up and bidirectional sequencing. The primer “tails” M13F and M13R were used as sequencing primers . We sequenced the COI barcode from 18 D. iulia specimens, constituting all Thai and Dominican samples in our dataset. We added 28 additional D. iulia barcode sequences from Costa Rica, Mexico, and Panama and a sequence from the outgroup Dryadula phaetusa (Nymphalidae: Heliconiinae) to the genetic dataset. We included all Dryas iulia sequences in GenBank that completely overlapped with the barcoding fragment that we sequenced; longer sequences were trimmed so that each sample included exactly 658 bp. The two Dominican specimens represent the subspecies D. iulia hispaniola. All other sequences, including those from Thailand, are of D. iulia modesta. Sequences from the other eleven D. iulia subspecies—which are mostly Caribbean island endemics—were unavailable. Sequences were viewed, assembled, aligned, and trimmed with Geneious ; alignments were performed within Geneious using MUSCLE . The sequence alignment is provided as a nexus file in Appendix S1. Protocols were adopted from dnabarcoding101.org, developed by the DNA Learning Center, Cold Spring Harbor Laboratory.
Phylogenetic and distance analyses
The most parsimonious haplotype network of D. iulia was determined with TCS 1.2 with a 95% connection limit , and redrawn using the Pie Graph Tool in Adobe Illustrator CS6 (adobe.com). The program jModelTest 2.1.4  was used to select the GTR+I+G model of sequence evolution using the AIC criterion, but we implemented the GTR+G model to avoid overparameterizing the data. A maximum likelihood analysis and an ML rapid bootstrap analysis were performed with RAxML 7.6.3  on the CIPRES Science Gateway (phylo.org) . Bootstrapping was stopped automatically using the majority rule criterion under a GTR+G model. Bayesian phylogenetic analyses were performed with MrBayes 3.2.2  on the CIPRES Science Gateway. Four Markov chains, one cold and three heated, were run simultaneously for 10 million generations. Trees were sampled every 1000 generations, and the first 25% of sampled trees were discarded as burn-in before calculating a consensus tree. Changes in the posterior probabilities of 20 nodes were plotted over the generations of the analysis with the program Are We There Yet?  in order to confirm that the chains had probably converged. To assess parsimony support for relationships among taxa, 1000 bootstrap replicates were run in TNT 1.1 using standard bootstrapping with replacement after “Max. trees” was reset to 10,000 . TaxonDNA 1.0 (taxondna.sourceforge.net)  was used to calculate uncorrected p-distances between barcode sequences.
DNA barcode sequences were identical among all specimens from Thailand: the single wild-caught Dryas iulia on Koh Phi Phi Don, the six wild-caught specimens on Koh Samui, and all nine specimens obtained from the Phuket Butterfly Garden (Fig. 2a). This 658 bp haplotype was not shared with any specimens caught in the New World, but was most similar to a Costa Rican specimen (1 bp difference). The tree topologies obtained from Bayesian, maximum likelihood, and parsimony methods were similar and had universally poor branch support, as one might expect of a phylogeny based on a single gene sampled within a single species (Fig. 2b). Each of the two D. iulia hispaniola specimens sampled from the Dominican Republic had a unique haplotype; both were notably distinct from the other sampled haplotypes. Several haplotypes were found in both Mexico and Costa Rica, demonstrating genetic diversity within the subspecies D. iulia modesta.
a) Most parsimonious haplotype network of D. iulia constructed with 95% connection limit. The size of each circle is proportional to the number of specimens sharing that haplotype; the smallest circles represent a single haplotype and the largest, sixteen. The colors of the pie charts indicate proportional representation of the provenance of samples with that haplotype. Separation by a line indicates a single base pair difference between haplotypes; crosses represent haplotypes that would be 1 bp different than adjacent haplotypes, but were not sampled in this study. b) maximum likelihood bootstrap consensus tree of COI haplotypes from D. iulia and one outgroup. Codes refer to GenBank Accession Numbers and colors denote provenance of specimen collection. Numbers near selected nodes indicate refer to the following branch support values (maximum likelihood bootstrap support, Bayes posterior probability, parsimony bootstrap support, respectively): = 40, –, –; = 27, 0.62, –; = 20, –, –; = 27, 0.75, –; = 31, 0.98, –; = 26, 0.69, –; = 100, 1, 100; = 100, 1, 100.
It is likely that wild populations of Dryas iulia in Thailand originated from livestock at a butterfly farm, possibly from individuals that were intentionally released alive. One such farm, the Phuket Butterfly Garden (PBG), may be the source of the wild population, but without exhaustive sampling, we cannot rule out other such farms as potential sources of the naturalized wild Thai population. There are at least two alternative scenarios consistent with our results. It is possible that the D. iulia livestock at PBG was obtained from the same source as a second, unknown source that was responsible for the introduction—perhaps another butterfly farm in Southeast Asia unknown to us. Alternatively, D. iulia could have been introduced into the wild in Thailand where they became established and subsequently collected by PBG for propagation and sale. We consider both of these alternatives unlikely. We know of no other butterfly houses in Thailand that stock non-Asian species, including Nong Nooch Tropical Garden, Pattaya (nongnoochgarden.com), Siam Insect Zoo, Chiang Mai (malaeng.com), Bangkok Butterfly Garden and Insectarium, and Bai Orchid and Butterfly Garden in Chiang Mai. Access to import documentation or knowledgeable PBG staff members could confirm or refute the second possibility.
Identical sequences between wild-caught specimens and those from PBG are not due to lack of genetic diversity in the species or subspecies. We included all publicly available, homologous D. iulia barcode sequences in our dataset (which happened to all be from the subspecies D. iulia modesta), and the 30 sequences from non-Thai samples constitute 17 distinct haplotypes, demonstrating some degree of genetic variability within the species as a whole. The lack of genetic diversity within Thai D. iulia is consistent with a genetic bottleneck caused by a small founding population. This might have happened if a small number of individuals was imported to Thailand and used to found a colony at a butterfly house that eventually became inbred .
It is unclear how this novel introduction will affect wild populations of other organisms. The species has been observed feeding on Passiflora foetida, which is an invasive plant in Thailand, and the butterfly might therefore be a boon for biological control of this weed. However, herbivory by D. iulia might suppress populations of other species through consumptive competition. This vine also provides fodder for the native butterfly species Cethosia cyane and Vindula erota, as well as the alien species Acraea terpsicore ( = A. violae) , which could be adversely affected.
Naturalization of this exotic species in Thailand may not have dire ecological consequences. The Monarch butterfly, Danaus plexippus, dispersed across the Pacific Ocean from the Americas to Australia in the 19th century , . This relatively recent addition to Australia's biota does not seem to suppress populations of native species, particularly since the larvae feed on introduced plant species including Asclepias curassavica and Gomphocarpus fruticosus ( = Asclepias fruticosa) . Introduced insect species occasionally increase their host breadth to include plant species native to the area of introduction , and D. iulia might impact native vegetation if this occurs. Observations of the species are currently confined to peninsular Thailand and Malaysia. Wild D. iulia was first recorded in Asia only seven years ago, and the species may still be expanding its range. Continued live butterfly release at weddings and religious ceremonies may be fortifying wild populations and aiding range expansion.
There are several ecological dangers associated with butterfly houses. Most of these facilities do not breed butterflies for display. Instead, they are sent shipments of live pupae from butterfly farms by express mail. Many of these shipments cross international borders, as the majority of butterfly farms are in tropical countries and many butterfly houses are in temperate areas . A relatively small number of butterfly farms supply pupae for most of the world's butterfly houses, with large numbers of butterfly farms in Costa Rica, Malaysia, and the Philippines. This translocation of livestock opens the possibility that exotic species could escape into areas where they are not native, thereby introducing novel and potentially pestiferous lepidopteran species into natural ecosystems, as seems to have happened in Thailand. If an escapee is from a species found locally, interbreeding between introduced and native genotypes could disrupt locally co-adapted gene complexes. This insidious “biopollution” of a gene pool could be harmful to species with separate populations that are locally adapted to different conditions. Even if butterflies remain contained within the facilities designed to house them, lepidopteran parasites and pathogens harbored by the living, translocated pupae are smaller and not easily detected. Escape of these butterfly enemies into the wild could have profoundly negative consequences on local butterfly populations . However, it is possible that these risks can be offset to some degree by the potential for butterfly houses to educate the public about basic biology and the importance of wild insects and their habitats, which are threatened around the world .
In early 2014, PBG's website showed photographs of at least three different couples in wedding garb releasing butterflies from a cage, and at least one, live D. iulia specimen can be seen in each photograph (phuketbutterfly.com/wedding.php, accessed March 2014). In addition to release at weddings, thousands of butterflies are released annually into the Khao Phra Thaeo Wildlife Conservation Area in Phuket in a release ceremony orchestrated in part by PBG , . The Phuket Gazette, a local newspaper, has recorded videos of these events in which release of D. iulia can be observed , . In many parts of Asia, captive animals have been released into the wild for over 1,000 years as part of Buddhist rituals aimed at cultivating compassion for living beings . In recent decades, exotic species are readily available in live animal markets in Asia either as pets or food. Release of these non-native species has led to their establishment as invasive species in some areas –. For example, the American turtle Trachemys scripta, which is sold as food and frequently released into the wild, is now the most common turtle in every river in Taiwan . There are several initiatives to educate Buddhist monks and laity about the ecological dangers of animal release , , .
Whereas butterfly houses offer the advantages of conservation awareness and general education about the importance of biodiversity, there are few, if any, positive environmental aspects of intentional butterfly release. Species introduction, biopollution of natural gene pools, and introduction of novel butterfly enemies are all far more likely when fecund, living butterflies are intentionally released into the wild , . For these and other reasons, several authors have called for a ban on the release of butterflies at weddings –. Within the United States, USDA-APHIS releases specific guidelines regarding the butterfly species that can be legally released in each state  in order to reduce the likelihood of negative ramifications of live butterfly release. We concur with other authors – that the release of live butterflies at social or cultural events should be banned; the short-lived benefits do not justify the threats of long-term damage.
Our analyses suggest that the Neotropical butterfly Dryas iulia was introduced to Thailand by the Phuket Butterfly Garden (PBG), which breeds the species for live release at weddings and other public events. Most wild D. iulia locality records in Thailand and Malaysia are on tropical islands that are frequently the site of destination weddings: Phuket, Phi Phi Don, Samui, and Tioman. It is likely that PBG obtained livestock from a butterfly farm in Costa Rica (as evidenced by similarity of barcode sequences), and subsequent inbreeding at the PBG expunged genetic variation, if there was any in the founding population. Released specimens bred in the wild and began using Passiflora foetida as a larval host plant. The distribution of the species in Thailand currently encompasses thousands of square kilometers, and eradication efforts are unlikely to be successful, particularly since P. foetida is a common, invasive species, making it difficult to find all possible larval host plants for control purposes. To strengthen our conclusions regarding the provenance of the Thai stock, future studies might include more markers and obtain samples from the species' entire native range, which includes most islands of the Caribbean as well as northern South America. We suggest that Thai authorities prohibit the intentional release of live butterflies for commercial purposes and social functions, and regulate the importation of live animals for non-scientific purposes, including insects, to prevent similar introductions in the future.
We thank Neil Collier, Les Day, Sin Khoon Khew, Christie Sukhdeo, and the Phuket Butterfly Garden for sharing specimens and genetic material. We are grateful to Tim Bonebrake, Michael Boppré, Andrew Brownjohn, Les Day, Pisuth Ek-Amnuay, Sin Khoon Khew, Daniel J. Schmidt, Mark Stoeckle, and Richard I. Vane-Wright for providing comments on earlier versions of this paper. The DNA Learning Center at Cold Spring Harbor Laboratory provided some DNA barcoding supplies and protocols; Antonia Florio, Christine Marizzi, and Melissa Lee were particularly helpful. Kelvin Guerrero assisted with specimen collection in the Dominican Republic. Support for collaborative STEM education between the High School for Environmental Studies, AMNH, and CCNY was facilitated by the Cold Spring Harbor Laboratory's DNA Learning Center and Urban Barcoding Project.
Conceived and designed the experiments: DJL. Performed the experiments: NAB AP RMG EZM EWZ. Analyzed the data: NAB DJL. Contributed reagents/materials/analysis tools: DJL WS. Contributed to the writing of the manuscript: NAB DJL.
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