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Article

Biogeographical Patterns of Herbivore Arthropods Associated with Chenopodium quinoa Grown along the Latitudinal Gradient of Chile

by
Rodrigo A. Chorbadjian
1,*,
María I. Ahumada
1,
Francisco Urra
2,
Mario Elgueta
2 and
Todd M. Gilligan
3
1
Departamento de Ciencias Vegetales, Facultad de Agronomía e Ingeniería Forestal, Pontificia Universidad Católica de Chile, Santiago 7820436, Chile
2
Sección Entomología, Museo Nacional de Historia Natural, Casilla 787, Santiago 7820436, Chile
3
USDA-APHIS-PPQ-Science and Technology, Identification Technology Program, Fort Collins, CO 80526, USA
*
Author to whom correspondence should be addressed.
Plants 2021, 10(12), 2811; https://doi.org/10.3390/plants10122811
Submission received: 20 November 2021 / Revised: 11 December 2021 / Accepted: 16 December 2021 / Published: 19 December 2021
(This article belongs to the Special Issue Worldwide Evaluations of Quinoa—Biodiversity and Food Security under Climate Change Pressures)
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Abstract

:
Identifying the particular guilds of herbivore arthropods that affect the production of crops is key to developing sustainable pest-management strategies; however, there is incomplete information about the identity of herbivore arthropods that could potentially damage the production of both highland and lowland quinoa landraces grown in Chile. By both reviewing the literature and conducting field collections across a large latitudinal gradient, we generated an updated list of 43 herbivore arthropods associated with quinoa production in Chile. In general, most species are polyphagous feeders, and only seven are specialists. The number and identity of species varied in relation with the latitude, such that four distinctive assemblages of herbivores were identified, each containing 32, 27, 34, and 22 species between latitudes 18–26, 26–32, 32–40, and 40–44° S, respectively. The most northern production area (18–26° S) is affected by nine unique species, including the major quinoa pest Eurysacca quinoae Povolný (Lepidoptera: Gelechiidae). Similarly, the central area (32–40° S) contains four unique species, including Eurysacca media Povolný (Lepidoptera: Gelechiidae) and Orthotylus flavosparsus (Sahlberg) (Hemiptera: Miridae). The particular species assemblages described here will help further development of local pest-management practices.

1. Introduction

Quinoa (Chenopodium quinoa Willd.) is an annual plant mainly grown to obtain grains for human consumption. The interest in cultivating this crop has increased in recent years due to its high nutritional value and its tolerance to soil salinity and drought stress [1,2,3]. Quinoa is cultivated over a wide variety of environments in South America, extending from the high altitudes (>3500 m above sea level (m.a.s.l.)) of the Andean Altiplano areas of Bolivia, Chile, and Perú, to the lowland/coastal areas of Chile and Perú [4,5]. Two distinctive quinoa ecotypes are cultivated in Chile, the salares and the coastal ecotypes [4]. Plants belonging to the salares ecotype grow in the northern region of Chile (18–29° S), which is separated from the central and southern regions (33–43° S) by the Atacama Desert and is agroecologically more similar to the Altiplanos of Perú and Bolivia. In the central and southern production regions, the coastal ecotype of quinoa is produced along with many other agricultural vegetables, crops, and fruit trees. Regarding the distribution of quinoa cultivation in Chile, the northern zone (17–26° S) accounted for 31%, the central zone (29–36° S) accounted for 64%, and the southernmost zone (37–44° S) accounted for 5% of total production during the years 2015–2016 [6].
The variety of agroecological environments over which quinoa is cultivated can influence the diversity of arthropods that negatively affect its production. For instance, while species of Eurysacca (quinoa moth, Lepidoptera: Gelechiidae) are more frequently indicated as a major pest in the highlands [5,7,8], other species such as thrips (Frankliniella occidentalis (Pergande) (Thysanoptera: Thripidae)), aphids (Macrosiphum euphorbiae (Thomas) (Hemiptera: Aphididae)), and leafminers (Liriomyza huidobrensis Blanchard (Diptera: Agromyzidae)) add to the array of pest species than can reach high populations in lowland areas of Perú [9].
Understanding the herbivore communities is essential to developing sustainable insect pest management strategies in quinoa production; however, specific studies reporting insect species that feed on quinoa in Chile are scarce and incomplete. For instance, the general compendium of insect pests of economic importance in Chile published by Artigas [10] reported only five insect species that use quinoa as a host plant. A few years later, Lamborot et al. [11] reported five Lepidoptera species found in quinoa grown in central Chile. Later, another compendium of arthropod species found in Chilean agricultural plants reported only eight taxa [12]. Finally, Logarzo et al. [13] reported the finding of one leafhopper species on quinoa in the Chilean Altiplano area. Clearly, this is a low number of species when compared with the potential 78 arthropod taxa reported by Cruces et al. [5] in a recent compilation of quinoa pests that included: 29 species of Lepidoptera, 22 Hemiptera, 16 Coleoptera, 4 Orthoptera, 3 Thysanoptera, 3 Diptera, and 1 Acari.
Because many insect species previously reported to feed on quinoa in other countries are also present in Chile, we decided to review and update this information. The underlying hypothesis is that it will be possible to identify distinct clusters of herbivore arthropods along the latitudinal gradient where quinoas are cultivated in Chile. In addition, we expected to identify latitudinal patterns in host range use, feeding habit, and geographical origin of these arthropods. Hence, the objective of this work was to generate an updated list of arthropod species associated with quinoa production in Chile by both reviewing the literature and conducting field collections on quinoa fields across a latitudinal gradient in a variety of agroecosystems. To further characterize the community of herbivores, species were classified according to their geographical origin and host-range use (i.e., generalist or specialist).

2. Results

Bibliographical evidence, together with field collections conducted in this study, allowed us to construct an updated list of arthropod herbivores that feed on quinoa plants in Chile, resulting in a total of 43 arthropod taxa. Across all latitudes, Lepidoptera is represented with 20 taxa in 4 families (Coleophoridae, Crambidae, Gelechiidae, and Noctuidae), Hemiptera with 15 taxa in 8 families (Aphididae, Cicadellidae, Coreidae, Lygaeidae, Miridae, Pentatomidae, Rhopalidae, and Triozidae), Coleoptera with 3 taxa in 3 families (Chrysomelidae, Curculionidae, and Meloidae), Thysanoptera with 2 Thripidae species, 1 Diptera (Agromyzidae), 1 Orthoptera (Acrididae), and 1 mite species (Acari: Tetranychidae) (Table 1).
During field collections, we found and identified 19 taxa. Species identified included, Achyra similalis (Guenée) (Lepidoptera: Crambidae), Agrotis ipsilon (Hufnagel) (Lepidoptera: Noctuidae), Aphis craccivora Koch (Hemiptera: Aphididae), Eurysacca quinoae Povolný (Lepidoptera: Gelechiidae), Frankliniella occidentalis (Thysanoptera: Thripidae), Feltia subterranea (Fabricius) (Lepidoptera: Noctuidae), Helicoverpa atacamae Hardwick (Lepidoptera: Noctuidae), Helicoverpa gelotopoeon (Dyar) (Lepidoptera: Noctuidae), Liorhyssus lineatoventris (Spinola) (Hemiptera: Rhopalidae), Liriomyza huidobrensis (Diptera: Agromyzidae), Macrosiphum euphorbiae (Hemiptera: Aphididae), Myzus persicae (Sulzer) (Hemiptera: Aphididae), Orthotylus flavosparsus (Sahlberg) (Hemiptera: Miridae), Tetranychus urticae Koch (Acari: Tetranychidae), Trichocyphus rubricollis (Blanchard) (Coleoptera: Curculionidae), and Trichoplusia ni (Hübner) (Lepidoptera: Noctuidae). Three taxa were included only at the level of genera, as there was uncertainty regarding their species names. Specifically, further research is needed to clarify species identity for Epitrix sp. (Coleoptera: Chrysomelidae), Pseudomeloe sp. (Coleoptera: Meloidae), and Copitarsia spp. (Lepidoptera: Noctuidae). Specimens of these three genera were collected in this study and saved for further taxonomic analyses.
The number of individual taxonomic units collected on each locality was 9 in the region of Tarapacá (Ancovinto site, 19° S), 13 in the Metropolitan region (Santiago and Pirque sites, 33° S), 7 in the O’Higgins region (Cahuil and Pailimo sites, 34° S), and 2 in the Los Lagos Region (Ancud sites, 42° S) (Table 1). Lepidoptera species were particularly abundant at the Ancovinto site. The identity of the quinoa moth Eurysacca quinoae was confirmed based on male genitalia structures that corresponded with its original description; particularly, the parabasal processes with broadly rounded clavate tips, symmetrical lanceolate saccular processes with an acute tip, and a long and slender valve [28]. Two species of Helicoverpa, H. atacamae and H. gelotopoeon, were confirmed based on morphological structures in comparison with descriptions and illustrations in Hardwick [30]. In particular, the two can be separated by the length of the male valvae, the shape of the everted vesica, and differences in setae on the foretibia [30]. We also identified a new host record for Trichocyphus rubricollis. Trichocyphus rubricollis was originally described by Kuschel [31] as a variety of T. formosus, to later recognize them as different specific entities [32]; Although Lanteri [33] establishes the synonymy between both names, Elgueta and Marvaldi [23] consider both as valid species. A few adults of T. rubricollis were detected feeding on quinoa leaves, chewing from the external margin of the leaves towards the central vein. Other species detected in this area included Copitarsia sp., Aphis craccivora, Macrosiphum euphorbiae, Liriomyza huidobrensis, and Pseudomeloe sp.
In the central area (Metropolitana and O’Higgins areas), specimens collected included: Achyra similalis, Agrotis ipsilon, Aphis craccivora, Copitarsia spp., Epitrix sp., Feltia subterranea, Frankliniella occidentalis, Liorhyssus lineatoventris, Liriomyza huidobrensis, Macrosiphum euphorbiae, Myzus persicae, Orthotylus flavosparsus, Tetranychus urticae, and Trichoplusia ni. Among these species, a complex of chinch bugs (L. lineatoventris and O. flavosparsus), Copitarsia spp., and L. huidobrensis were more frequently collected. Our results also provide new information for the distribution range of O. flavosparsus, as it was known to be present in Chile [22], but no information on its distribution range and host use had been reported. In turn, the southernmost area of Ancud is characterized by the presence of fewer herbivore species. Here, we only collected Copitarsia spp. and M. euphorbiae. While only a few specimens of M. euphorbiae were detected, Copitarsia caterpillars were found more often but still in low numbers.
Regarding the total number of species expected to affect quinoa in Chile, we found that species assemblages varied in relation to the geographical region. Cluster analysis identified four groups with a percentage of similarity higher than 80% within each cluster (Figure 1). One cluster grouped the regions of Arica y Parinacota, Tarapacá, and Antofagasta (18–26° S) with 32 taxa; a second cluster included 27 taxa in the regions of Atacama and Coquimbo (26–32° S). In the central area of Chile, a third cluster included 34 taxa in the Regions of Valparaíso, Metropolitana, O’Higgins, Maule, Ñuble, Bio-Bío and Araucanía (32–40° S), and the fourth cluster assembled 22 taxa in the regions of Los Rios and Los Lagos (40–44° S) (Table 2). Interestingly, both Cluster 1 and 3 included unique species. Cluster 1 is defined by nine species that are uniquely found in the northernmost region, which is closest to the borders with Perú and Bolivia. This is the case for Agrotis experta (Walker) (Lepidoptera: Noctuidae), Anacuerna centrolinea (Melichar) (Hemiptera: Cicadellidae), Chrysodeixis includens (Walker) (Lepidoptera: Noctuidae), Eurysacca quinoae, Pseudomeloe sp., Spodoptera frugiperda (J.E. Smith) (Lepidoptera: Noctuidae), Spodoptera ochrea (Hampson) (Lepidoptera: Noctuidae), Spoladea recurvalis (Fabricius) (Lepidoptera: Crambidae), and Trichocyphus rubricollis. Similarly, Cluster 3 in the central region is uniquely defined by the presence of Coleophora versurella Zeller (Lepidoptera: Coleophoridae), Epitrix sp., Eurysacca media Povolný (Lepidoptera: Gelechiidae), and Orthotylus flavosparsus.
In general, most species that feed on quinoa in Chile have a wide range of host use, given that 33 of them are polyphagous (77%) and only 7 are specialists (16%) (Table 1). When their geographical distribution is analyzed as a variable, the proportion of specialist herbivores ranges between 5 and 15% between parallels 18 and 39° S, with the lowest proportion in the southernmost area delimited by parallels 40–44° S (Figure 2). The distribution of the specialist herbivores Eurysacca quinoae, E. media, Coleophora versurella, and Heterotrioza chenopodii (Reuter) (Hemiptera: Triozidae) highly influenced this pattern due to their absence in the southern latitudes of Chile.
The feeding habit of the arthropod species that attack quinoa in Chile is mostly dominated by chewing and piercing–sucking insects. The relative proportion of chewing insects ranges between 44 and 60%, and that of piercing–sucking hemipterans between 28 and 41%, depending on the geographical area (Figure 2). Only three species puncture plant cells, including two thrips (F. occidentalis and Thrips tabaci Lindeman) and the two-spotted spider mite (T. urticae). The leafminer L. huidobrensis was the only species identified with this strict feeding habit, which is distributed across the entire Chilean territory (Table 1). Eurysacca species were classified as chewer insects, although it has been reported that they have a leaf-mining habit during the early stages of larval development [7].
Regarding the geographical origin of the 43 arthropod species reported to feed on quinoa in Chile (Table 1), 30 species are native to the New World, while only 2 are Palearctic, and 1 comes from the Indo-Malayan realm. Interestingly, Oncopeltus miles (Blanchard) (Hemiptera: Lygaeidae) is the only native species reported to feed on quinoa in Chile [10]. In turn, 10 species have an uncertain geographical origin, as these are cosmopolitan agricultural pests (Table 1).

3. Discussion

This is the first study to compile a list of arthropods that feed on quinoa in Chile, which will help quinoa growers and future insect–plant interaction research. Until this study, only 10 insect species had been reported as quinoa feeders within the Chilean territory. Specifically, the general compendium of insect pests of economic importance in Chile reported one aphid (Smynthurodes betae Westwood (Hemiptera: Aphididae)), one chinchbug (O. miles), and three Lepidoptera species (Helicoverpa zea (Boddie), Rachiplusia nu Guenée, and S. recurvalis) [10]. Another study that focused on caterpillars reported five Lepidoptera species found in quinoa in central Chile, including E. media, Copitarsia turbata (Herrich-Schäffer), R. nu, C. versurella, and A. similalis [11]. The most recent compendium of arthropod species found in Chilean agricultural plants reported a total of 8 taxa, including Copitarsia sp., H. zea, O. miles, R. nu, Sigelgaita chilensis Heinrich, S. betae, S. recurvalis, and Tapajosa sp. [12]. However, we found a few incorrect species names and host use attributions in Klein-Koch and Waterhouse [12] and made appropriate corrections to construct Table 1. Specifically, Sigelgaita chilensis Heinrich does not feed on quinoa [10]; thus, it was not included here. Additionally, Klein-Koch and Waterhouse [12] lists Tapajosa sp. as a quinoa feeder, but as stated by Logarzo et al. [13], Tapajosa sp. was identified later as A. centrolinea. Finally, there is uncertainty about the identity of the species reported as C. turbata [11] because there is considerable confusion among Copitarsia species in South American literature [34]. Therefore, all individuals identified as Copitarsia during the conduction of this study are reported here as Copitarsia spp. and were saved for further taxonomic analysis.
It is possible that other insect species also feed on quinoa in Chile, but for which further studies are needed to clarify its potential presence on quinoas in Chile. For instance, this is the case for the genera Rhinacloa (Miridae), Xenogenus (Rhopalidae), Empoasca (Cicadellidae), Bergallia (Cicadellidae), Conoderus (Elateridae), Cylydrorhinus (formerly = Adioristus) (Curculionidae), Tetraonyx (Meloidae), and Symmetrischema (Gelechiidae). Specifically, regarding Rhinacloa sp. reported from the Altiplano area [7,16], there are five species in Chile, including R. aricana Carvalho, R. azapa Schuh and Schwartz, R. incaicus (Carvalho and Gomes), R. penai Schuh and Schwartz, and R. peruana Schuh and Schwartz [22]. The species Xenogenus picturatum Berg. was reported on quinoa [5,15], but only Xenogenus gracilis (Reed) is present in Chile [10]. Likewise, the genera Empoasca and Bergallia (Cicadellidae) have been reported attacking quinoa in Perú [35], for which Empoasca curveola Oman [10] and Bergallia valdiviana Berg [36] are found in Chile, but we did not find evidence of their association with the cultivation of quinoa in Chile. Similarly, Dughetti [15] and Cruces et al. [5] also report Conoderus sp. on quinoa; however, we did not find either Conoderus chilensis (Schwartz) or C. rufangulus (Gyllenhal), which are the two species present in Chile [10]. Another taxon previously reported only at the level of genus is Adioristus sp. [5,7,16], but this name is a synonym of Cylydrorhinus, as stated by Wibmer and O’Brien [37]. Valoy et al. [38] reported Tetraonyx sp. with no details about species identity. For this genus in Chile, Elgueta and Arriagada [39] reported Tetraonyx limbata, T. parviceps and T. septemguttata, however there is no information that suggests quinoa as part of their host range. Regarding another potential quinoa pest, Dughetti [15] and Cruces et al. [5] also reported Symmetrischema sp., for which S. nanum Povolný, S. striatella (Murtfeldt), and S. tangolias (Gyen) are in Chile [26,40,41]. Undoubtedly, future samplings and taxonomic studies could expand the list of species reported in this study.
Most species that feed on quinoa are chewing stages belonging to Lepidoptera and a few species of Coleoptera and Orthoptera, followed by piercing–sucking Hemiptera. Insects with a chewing feeding habit feed on leaves, inflorescences, and developing grains. Flower- and seed-feeding insects, such as Gelechiidae and Noctuidae, often cause serious damage to quinoa production [5,7,16]. Piercing–sucking hemipterans, such as Aphididae and Cicadellidae, feed on phloem/xylem sap extracted from leaves, stems, and inflorescences, while chinch bugs in Heteroptera may also feed on immature grains [15]. In contrast, Thysanoptera species can puncture and extract cell contents of leaves, buds, inflorescences, and pollen. Agromyzidae species use a different feeding strategy, as the larvae of L. huidobrensis construct feeding galleries in the leaves of quinoa, and adult females puncture the leaves with their ovipositor to feed on cell content [5]. The larvae of a few species feed underground, such as Epitrix and those belonging to Anthomyiidae [5,18].
Although a variety of insects feed on quinoa, some are rarely seen in the field [9]. Additionally, only a few species are commonly observed in high population numbers, thereby causing concerns to growers about potential yield losses [5,7,9]. Typically, Eurysacca melanocampta (Meyrick) and E. quinoae are frequently cited as the most significant quinoa pests in Perú and Bolivia [5,7]. Nonetheless, the geographical location of quinoa production has been shown to influence species richness and its abundance, even within the same country. In a recent study conducted in two lowland sites (La Molina and Majes) and one highland site (San Lorenzo) of Perú, Cruces et al. [9] detected higher populations of M. euphorbiae, E. melanocampta, and L. huidobrensis in La Molina, as well as of F. occidentalis in the locality of Majes; only E. melanocampta was a major pest in San Lorenzo. Concordantly, we identified four distinct groups of species associated with quinoa along a latitudinal gradient of Chile (Table 2). Nine unique insect species feed on quinoa in the northern territory (Cluster 1), including A. experta, A. centrolinea, C. includens, E. quinoae, Pseudomeloe sp., S. frugiperda, S. ochrea, S. recurvalis, and T. rubricollis. This geographic area is close to the borders with Perú and Bolivia, and it is geographically isolated from the central and southern quinoa production areas by the Atacama Desert. Indeed, many of these species are also reported from the Altiplano areas of Bolivia and Perú [5]. During our observations in the quinoas grown in the altiplano area of Ancovinto, we found relatively high numbers of E. quinoae, H. atacamae, H. gelotopoeon, and Copitarsia sp. larvae feeding on leaves, flowers, and developing grains, as well as occasional clusters of the aphid A. craccivora during grain development, but otherwise, other species were uncommon.
Coastal ecotypes grown at higher latitudes are potentially affected by a distinct assemblage of insect species. Particularly, the central region (Cluster 3) concentrates the highest number of species, with unique species including E. media, Epitrix sp., O. flavosparsus, and C. versurella. Nonetheless, not all the species present in this area have been signified as major pests in other lowland areas of quinoa production [9]. Indeed, during our field studies, we only observed population outbreaks of Copitarsia sp., L. lineatoventris, and O. flavosparsus, as well as occasional infestations with A. craccivora and L. huidobrensis. In the southernmost production area (Cluster 4), the number of herbivorous arthropod species is the lowest, therefore representing potential advantages for the sustainable production of quinoa at higher latitudes.
Most species potentially found on quinoa in Chile show a wide range of host use. Generalist herbivores are often major pests in other agricultural crops, and therefore, they could potentially colonize quinoas grown near vegetables and other crop species as quinoa production areas diversify outside the highlands of the Andes. This has been reported in Perú, where lowland quinoas are negatively affected by polyphagous feeders such as F. occidentalis, M. euphorbiae, and L. huidobrensis [9]. Similarly, several polyphagous insect species negatively affect quinoas in other countries, such as Argentina [15], the United States [18], and Italy [42,43,44]. Interestingly, many of these generalist feeders are also cosmopolitan invasive pests that represent potential pest problems in other areas of the world where quinoa production is expanding.

4. Materials and Methods

4.1. Field Sampling and Species Identification

Commercial and experimental quinoa plantations were sampled periodically between 2015 and 2018 in 7 sampling sites within the 4 political regions named (abbr.) Tarapacá, Metropolitana, O’Higgins, and Los Lagos. For each region, sampling details are provided below.
  • Tarapacá
  • Ancovinto site with commercial plantations of salares ecotype (20 ha) (19°24′ S, 68°35′ W, 3720 m.a.s.l.). Inspected: 10 December 2016, 27 January 2017, 7 April 2017, and 29 January 2018.
  • Metropolitana
  • Pirque site. Research facility with experimental plantations (1 ha) of coastal ecotype (33°40′ S, 70°35′ W, 653 m.a.s.l.). Inspected: 22 December 2015, 14 January 2016, and 10 October 2018.
  • Santiago site, research facility with demonstrative plantation of coastal ecotype (33°29′ S, 70°36′ W, 576 m.a.s.l.). Inspected on a monthly basis from November through April of 2016, 2017, and 2018.
  • O’Higgins
  • Cahuil site with commercial plantation of coastal ecotype (10 ha) (34°29′, 72°01′ W, 40 m.a.s.l.). Inspected: 12 October 2016, 12 December 2016, 12 January 2016, and 22 January 2017.
  • Pailimo site with commercial plantation of coastal ecotype (5 ha) (34°15′ S, 71°47′ W, 242 m.a.s.l.). Inspected: 12 October 2016, 12 January 2016, and 22 January 2017.
  • Los Lagos
  • Ancud sites 1 and 2 with commercial plantations of coastal ecotypes (0.1 and 0.2 ha) (41°50′ S, 74°00′ W, 7 m.a.s.l., and 42°00′ S, 73°53′ W, 38 m.a.s.l.). Inspected: 16 December 2016, 13 January 2017, and 3 February 2017.
In these sites, quinoa plants were scouted by whole-plant visual inspections, plant beating, and using a sweeping net. Similar sampling efforts were devoted to each sampling date, which corresponded to 1 h of scouting. Special attention was given to collecting insects that were actively feeding. For inspections, each site was monitored in a random pattern, selecting at least 5 sectors where 5–10 plants were sampled per sector. Plant tissues affected by each species were annotated as leaves, stems, and/or panicles (flowers and/or seeds). Immature stages were brought to the laboratory and reared individually until adult emergence. Identifications of field-collected specimens were conducted on mounted adult specimens and comparing their morphological traits with available taxonomic publications [10,23,27,28,30,31,32,33,45,46,47], or directly with identified specimens in the Colección Nacional de Insectos, Museo Nacional de Historia Natural, Santiago, Chile (MNNC). Voucher specimens are conserved in the Entomological Collection of the Museo Nacional de Historia Natural, Santiago, Chile and in the Entomological Collection of Facultad de Agronomía e Ingeniería Forestal, Pontificia Universidad Católica de Chile, Santiago.

4.2. Total Number of Expected Species

First, we compiled records of insect and mite species to create a comprehensive list of arthropods reported to feed on quinoa around the world. We used the following scientific articles, books, and technical reports: [5,7,10,11,15,16,18,38,41,48]. Thereafter, this list was checked for the correct use of scientific names and updated. Arthropod species names were checked against currently available records for species present in Chile and updated with the species found in the surveys conducted in this study.
This checklist of arthropods associated with quinoa production in Chile was supplemented with bibliographical information about their geographical distribution in Chile, as well as their feeding habits and host range. Feeding habits were classified according to their mouthparts into chewing, piercing–sucking, cell-puncturing, and leaf-mining habits. Host range use was classified either as generalist or specialist if the species had been reported feeding on several non-related plant genera or only on a few related plant species [49]. Additionally, the species were classified according to their geographical origin into Nearctic (North America), Neotropic (Central and South America), Nearctic—Neotropic (American continent in general), Palearctic (Eurasia), Indo-Malayan (India—Asia), Chile (Native), or as unknown [10,13,20,27,28,50].

4.3. Data Analysis

Multivariate cluster analysis was conducted to find associations among species according to their presence/absence within each political region of Chile (latitudinal variables). Data matrix was constructed using the presence or absence (values 1 or 0, respectively) of the 43 arthropod taxa (reported in Table 1) in each of the 14 political regions that represent the variety of environments where quinoa is produced in Chile, specifically: Región de Arica y Parinacota (~17.5–19.1° S), Región de Tarapacá (~19.2–21.6° S), Región de Antofagasta (~21.7–25.8° S), Región de Atacama (~25.9–29.2° S), Región de Coquimbo (~29.3–32° S), Región de Valparaíso (~32.1–33° S), Región Metropolitana de Santiago (~33.1–34° S), Región del Libertador General Bernardo O’Higgins (~34.1–34.8° S), Región del Maule (~34.9–36.2° S), Región de Ñuble (~36.2–36.9° S), Región del Bio-Bio (~36.9–37.8° S), Región de La Araucanía (~37.9–39.5° S), Región de Los Ríos (~39.5–40.4° S), and Región de Los Lagos (~40.4–43.7° S). A dendrogram was constructed by distance correlation coefficient and complete linkage amalgamation steps functions using Minitab 17 software (Minitab Inc., State College, PA, USA). Specifically, for the linkage method, the distance between two clusters was calculated with the furthest-neighbor method, which is the maximum distance between variables of one cluster relative to another cluster. Distance between variables was calculated using the correlation method to consider positively correlated data to be closer than negatively correlated data, as it calculates distances between 0 and 1 for positive correlations and values between 1 and 2 for negative correlations. A total of 13 amalgamation steps were considered to create the dendrogram. Similarity levels ranged between 100 (13 clusters) and 91.3% (7 clusters) for the first 7 steps, and between 88.2 to 85.8% for steps 8 (6 clusters) to 10 (4 clusters), after which the similarity dropped below 74%.

Author Contributions

Conceptualization, methodology, formal analysis, data curation, writing—original draft preparation, R.A.C. and M.I.A.; resources, R.A.C.; investigation, writing—review and editing, R.A.C., M.I.A., F.U., M.E., and T.M.G. All authors have read and agreed to the published version of the manuscript.

Funding

This research was partially supported by funds provided by Fundación para la Innovación Agraria and Fondo de Innovación para la Competitividad (FIA EST-2016-0079, FIA EST-2016-0080, FIC PYT-2016-0450).

Data Availability Statement

Data is contained within the article.

Acknowledgments

We appreciate the help provided by Francisco Fuentes, Pablo Olguin, and Claudia Rojas to collect samples, as well as Audrey Grez for comments on an earlier version of this manuscript. We also thank Eduardo Faúndez for his assistance with Heteroptera. We also appreciate the following persons for allowing us to collect samples in their quinoa fields: Cecilia Guineo, Pilar Cárcamo, Lucia Araneda, Lautaro Díaz, and Abimael Gómez.

Conflicts of Interest

The authors declare no conflict of interest. The funders had no role in the design of the study; in the collection, analyses, or interpretation of data; in the writing of the manuscript, or in the decision to publish the results.

References

  1. Fuentes, F.; Bhargava, A. Morphological analysis of quinoa germplasm grown under lowland desert conditions. J. Agron. Crop Sci. 2011, 197, 124–134. [Google Scholar] [CrossRef]
  2. Miranda, M.; Vega-Gálvez, A.; Martinez, E.A.; López, J.; Marín, R.; Aranda, M.; Fuentes, F. Influence of contrasting environment on seed composition of two quinoa genotypes: Nutritional and functional properties. Chil. J. Agric. Res. 2013, 73, 108–116. [Google Scholar] [CrossRef]
  3. Fuentes, F.; Paredes-González, X. Nutraceutical Perspectives of Quinoa: Biological Properties and Functional Applications. In State of the Art Report on Quinoa around the World in 2013; Bazile, D., Bertero, H.D., Nieto, C., Eds.; FAO & CIRAD: Rome, Italy, 2015; pp. 286–299. [Google Scholar]
  4. Fuentes, F.F.; Martinez, E.A.; Hinrichsen, P.V.; Jellen, E.N.; Maughan, P.J. Assessment of genetic diversity patterns in Chilean quinoa (Chenopodium quinoa Willd.) germplasm using multiplex fluorescent microsatellite markers. Conserv. Genet. 2009, 10, 369–377. [Google Scholar] [CrossRef]
  5. Cruces, L.M.; Callohuari, Y.; Carrera, C. Quinua Manejo Integrado de Plagas. Estrategias en el Cultivo de la Quinua Para Fortalecer el Sistema Agroalimentario en las Zonas Andinas; Organización de las Naciones Unidas para la Alimentación y la Agricultura: Santiago, Chile, 2016; pp. 1–198. [Google Scholar]
  6. Fuentes, F.F.; Olguín, P.; Duarte, L.; Ojeda, M.; Figueroa, C.; Paredes-González, X.; Martínez, E.A. Potencial Competitivo de la Quinua Chilena; Publicaciones Fundación para la Innovación Agraria: Santiago, Chile, 2017; pp. 1–147. [Google Scholar]
  7. Rasmussen, C.; Lagnaoui, A.; Esbjerg, P. Advances in the knowledge of quinoa pests. Food Rev. Int. 2003, 19, 61–75. [Google Scholar] [CrossRef] [Green Version]
  8. Saravia, R.; Plata, G.; Gandarillas, A. Plagas y Enfermedades del Cultivo de Quinua; Fundación PROINPA: Cochabamba, Bolivia, 2014; pp. 1–148. [Google Scholar]
  9. Cruces, L.; de la Peña, E.; De Clercq, P. Seasonal phenology of the major insect pests of quinoa (Chenopodium quinoa Willd.) and their natural enemies in a traditional zone and two new production zones of Peru. Agriculture 2020, 10, 644. [Google Scholar] [CrossRef]
  10. Artigas, J.N. Entomología Económica; Ediciones Universidad de Concepción: Concepción, Chile, 1994; Volumes I and II, pp. 1–1126 and 1–943. [Google Scholar]
  11. Lamborot, L.; Guerrero, M.A.; Araya, J.E. Lepidópteros asociados al cultivo de la quinoa (Chenopodium quinoa Willdenow) en la zona central de Chile. Bol. San. Veg. Plagas 1999, 25, 203–207. [Google Scholar]
  12. Klein-Koch, C.; Waterhouse, D.F. Distribución e importancia de los artrópodos asociados a la agricultura y silvicultura en Chile. ACIAR Monogr. 2000, 68, 1–234. [Google Scholar]
  13. Logarzo, G.A.; De León, J.H.; Triapitsyn, S.V.; González, R.H.; Virla, E.G. First report of a Proconiine Sharpshooter, Anacuerna centrolinea (Hemiptera: Cicadellidae), in Chile, with notes on its biology, host plants, and egg parasitoids. Ann. Entomol. Soc. Am. 2006, 99, 879–883. [Google Scholar] [CrossRef]
  14. Elgueta, M.; Camousseight, A.; Carbonell, C.S. Catálogo de Orthoptera (Insecta) de Chile; Publicación Ocasional Nº 54; Museo Nacional de Historia Natural: Santiago, Chile, 1999; pp. 1–60. [Google Scholar]
  15. Dughetti, A.C. Plagas de la Quinua y sus Enemigos Naturales en el Valle Inferior del Río Colorado, Buenos Aires, Argentina, 1st ed.; Ediciones INTA: Buenos Aires, Argentina, 2015; pp. 1–63. [Google Scholar]
  16. Gandarillas, A.; Saravia, R.; Plata, G.; Quispe, R.; Ortiz-Romero, R. Principales plagas y enfermedades de la quinua. In State of the Art Report on Quinoa around the World in 2013; Bazile, D., Bertero, H.D., Nieto, C., Eds.; FAO & CIRAD: Rome, Italy, 2015; pp. 192–215. [Google Scholar]
  17. Nieto-Nafría, J.M.; Fuentes-Contreras, E.; Castro Colmenero, M.; Aldea Piera, M.; Ortego, J.; Mier Durante, M.P. Catálogo de los áfidos (Hemiptera, Aphididae) de Chile, con plantas hospedadoras y distribuciones regional y provincial. Graellsia 2016, 72, e050. [Google Scholar] [CrossRef] [Green Version]
  18. Cranshaw, W.S.; Kondratieff, B.C.; Qian, T. Insect associated with Quinoa, Chenopodium quinoa, in Colorado. J. Kans. Entomol. Soc. 1990, 63, 195–199. [Google Scholar]
  19. Burckhardt, D. Generic key to Chilean jumping plant-lice (Homoptera: Psylloidea) with inclusion of potential exotic pests. Rev. Chil. Entomol. 1994, 21, 57–67. [Google Scholar]
  20. Faúndez, E.I.; Rocca, J. Descripción de un caso teratológico en Oncopeltus (Erythrischius) miles (Blanchard, 1852) (Heteroptera: Lygaeidae) con notas acerca de su distribución y biología. Arq. Entomol. 2016, 15, 39–43. [Google Scholar]
  21. Faúndez, E.I.; Carvajal, M.A. Sobre la relación entre Leptoglossus chilensis (Spinola, 1852) y Leptoglossus concaviusculus Berg, 1892 stat. rest. (Heteroptera: Coreidae), con nuevos datos acerca de su morfología. An. Inst. Patagon. 2016, 44, 65–70. [Google Scholar] [CrossRef] [Green Version]
  22. Prado, E. Conocimiento actual de Hemiptera—Heteroptera de Chile con lista de especies. Bol. Mus. Nac. Hist. Nat. Chile 2008, 57, 31–75. [Google Scholar]
  23. Elgueta, M.; Marvaldi, A.E. Lista sistemática de las especies de Curculionoidea (Insecta: Coleoptera) presentes en Chile, con su sinonímia. Bol. Mus. Nac. Hist. Nat. Chile 2006, 55, 113–153. [Google Scholar]
  24. Frías, D.; Henry, A.; Alviña, A.; Landry, J.F. Aspectos de la biología, taxonomía y control de las especies del género Coleophora (Lepidoptera: Coleophoridae) de distribución chilena. Acta Entomol. Chil. 1996, 20, 115–122. [Google Scholar]
  25. Guerrero, M.A.; Lamborot, L.; Araya, J.E. Observaciones biológicas de Achryra similalis (Guenèe) (Pyralidae) y otros lepidópteros en amaranto, Amaranthus cruentus L. (Amaranthaceae), en la Región Metropolitana de Chile. Bol. San. Veg. Plagas 2000, 26, 591–598. [Google Scholar]
  26. Cepeda, D.E. Contribution to the knowledge of Chilean Gelechiidae (Lepidoptera: Gelechioidea). Insecta Mundi 2017, 584, 1–8. [Google Scholar]
  27. Povolný, D. Gnorimoschemini of southern South America II: The genus Eurysacca (Lepidoptera, Gelechiidae). Steenstrupia 1986, 12, 1–47. [Google Scholar]
  28. Povolný, D. Eurysacca quinoae sp.n.—A new quinoa-feeding species of the tribe Gnorimoschemini (Lepidoptera, Gelechiidae) from Bolivia. Steenstrupia 1997, 22, 41–43. [Google Scholar]
  29. Angulo, A.O.; Weigert, G.T. Estados Inmaduros de Lepidópteros Nóctuidos de Importancia Económica en Chile y Claves Para su Determinación (Lepidoptera: Noctuidae); Publicación especial N°2; Sociedad de Biología de Concepción: Concepción, Chile, 1975; 153p. [Google Scholar]
  30. Hardwick, D.F. The corn earworm complex. Mem. Entomol. Soc. Can. 1965, 40, 1–247. [Google Scholar] [CrossRef]
  31. Kuschel, G. Los Curculionidae del extremo norte de Chile (Coleoptera. Curcul. Ap. 6°). Acta Zool. Lilloana 1949, 8, 5–54. [Google Scholar]
  32. Kuschel, G. New rank for varieties of Trichocyphus formosus. In Annotated Checklist of the Weevils (Curculionidae sensu lato) of South America (Coleoptera: Curculionoidea); Wibmer, G.J., O’Brien, N.C.W., Eds.; American Entomological Institute: Ann Arbor, MI, USA, 1986; Volume 39, p. 52. [Google Scholar]
  33. Lanteri, A.A. Estudio sistemático de los géneros Trichocyphus Heller y Mendozella Hustache (Coleoptera: Curculionidae). Bol. Soc. Biol. Concepción Chile 1989, 60, 139–147. [Google Scholar]
  34. Pogue, M.G. A review of the Copitarsia decolora (Guenée) (Lepidoptera: Noctuidae) species complex with the description of a new species from Chile and Argentina. Neotrop. Entomol. 2014, 43, 143–153. [Google Scholar] [CrossRef]
  35. Yábar, E.; Gianoli, E.; Echegaray, E.R. Insect pest and natural enemies in two varieties of quinoa (Chenopodium quinoa) at Cusco, Peru. J. Appl. Entomol. 2002, 126, 275–280. [Google Scholar] [CrossRef] [Green Version]
  36. Quiroga, N.; Longone, V.; González, X.; Zamorano, A.; Pino, A.M.; Picciau, L.; Alma, A.; Paltrinieri, S.; Contaldo, N.; Bertaccini, A.; et al. Transmission of 16SrIII-J phytoplasmas by the leafhoppers Paratanus exitiousus and Bergallia valdiviana. Phytopathol. Mediter. 2019, 58, 231–237. [Google Scholar]
  37. Wibmer, G.J.; O’Brien, N.C.W. Annotated checklist of the weevils (Curculionidae sensu lato) of South America (Coleoptera: Curculionoidea). Mem. Am. Entomol. Inst. 1986, 39, 1–563. [Google Scholar]
  38. Valoy, M.E.; Bruno, M.A.; Prado, F.E.; González, J.A. Insects associated to a quinoa crop in Amaicha del Valle, Tucumán, Argentina./Insectos asociados a un cultivo de quinoa en Amaicha del Valle, Tucumán, Argentina. Acta Zool. Lilloana 2011, 55, 16–22. [Google Scholar]
  39. Elgueta, M.; Arriagada, G. Estado actual del conocimiento de coleópteros de Chile (Insecta: Coleoptera). Rev. Chil. Entomol. 1989, 17, 5–60. [Google Scholar]
  40. Povolný, D. Gnorimoschemini of southern South America IV: The genus Symmetrischema (Lepidoptera, Gelechiidae). Steenstrupia 1989, 15, 57–104. [Google Scholar]
  41. Povolný, D. Gnorimoschemini of southern South America VI: Identification keys, checklist of Neotropical taxa and general considerations (Insecta, Lepidoptera, Gelechiidae). Steenstrupia 1994, 20, 1–42. [Google Scholar]
  42. Dioli, P.; Colamartino, A.D.; Negri, M.; Limonta, L. Hemiptera and coleoptera on Chenopodium quinoa. Redia 2016, 99, 139–141. [Google Scholar]
  43. Reguzzi, M.C.; Nicoli Aldini, R.; Vercesi, A.; Ganimede, C.; Tabaglio, V.; Mazzoni, E.; Dioli, P. Quinoa, quali insetti infestanti sono presenti al Nord Italia. L’Informatore Agrario 2019, 75, 59–61. [Google Scholar]
  44. Scaccini, D.; Furlan, L. Nysius cymoides (Hemiptera: Lygaeidae), a potential emerging pest: Overview of the information available to implement integrated pest management. Int. J. Pest Manag. 2021, 67, 73–88. [Google Scholar] [CrossRef]
  45. Göllner-Scheiding, U. Revision der Gattungen Liorhyssus STÅL, 1870 (Heteroptera, Rhopalidae). Dtsch. Entomol. Z. 1975, 23, 181–206. [Google Scholar] [CrossRef]
  46. Blackman, R.L.; Eastop, V.F. Aphids on the World’s Herbaceous Plants and Shrubs; John Wiley & Sons: Chichester, UK, 2006; pp. 1–1456. [Google Scholar]
  47. San Blas, G. Agrotis Ochsenheimer (Lepidoptera, Noctuidae): A systematic analysis of South American species. Zootaxa 2014, 3771, 1–64. [Google Scholar] [CrossRef]
  48. Wrzesinska, D.; Wawrzyniak, M.; Gesinski, K. Population of true bugs (Heteroptera) on the inflorescences of quinoa (Chenopodium quinoa Willd.). J. Plant Prot. Res. 2001, 41, 333–336. [Google Scholar]
  49. Schoonhoven, L.M.; van Loon, J.J.A.; Dicke, M. Herbivorous insects: Something for everyone. In Insect-Plant Biology, 2nd ed.; Oxford University Press Inc.: New York, NY, USA, 2005; pp. 5–28. [Google Scholar]
  50. San Blas, G. A morphological phylogeny of Agrotis Ochsenheimer (Lepidoptera, Noctuidae), with emphasis on the South American species. Zool. Scr. 2014, 44, 153–164. [Google Scholar] [CrossRef]
Plants 10 02811 g001 550
Figure 1. Dendrogram resulting from the multivariate cluster analysis of the geographical distribution variables of quinoa feeding arthropods present in Chile. Cluster description is presented in Table 2.
Figure 1. Dendrogram resulting from the multivariate cluster analysis of the geographical distribution variables of quinoa feeding arthropods present in Chile. Cluster description is presented in Table 2.
Plants 10 02811 g001
Plants 10 02811 g002 550
Figure 2. Latitudinal patterns of host range, feeding habit, and geographical origin of arthropod species that feed on quinoa in each latitudinal cluster of species.
Figure 2. Latitudinal patterns of host range, feeding habit, and geographical origin of arthropod species that feed on quinoa in each latitudinal cluster of species.
Plants 10 02811 g002
Table
Table 1. Species list and characteristics of herbivore arthropods that use quinoa as a host plant and are present in Chile.
Table 1. Species list and characteristics of herbivore arthropods that use quinoa as a host plant and are present in Chile.
SpeciesDistribution Range in Chile (° S)Feeding HabitHost RangeGeographical OriginReferences
Orthoptera: Acrididae
Dichroplus maculipennis (Blanchard, 1851)29–56ChewingGeneralistNeotropic[5,14,15]
Hemiptera: Cicadellidae
Anacuerna centrolinea (Melichar, 1925)19–22Piercing–suckingGeneralistNeotropic[5,13]
Paratanus exitiosus Beamer, 194332–41Piercing–suckingGeneralistNeotropic[5,7,10,16]
Hemiptera: Aphididae
Aphis craccivora Koch, 185418–44 a,b,cPiercing–suckingGeneralistPalearctic[5,7,10,15,16]
Aphis gossypii Glover, 187718–44Piercing–suckingGeneralistUnknown[5,7,12,16,17]
Macrosiphum euphorbiae (Thomas, 1878)18–56 a,b,c,dPiercing–suckingGeneralistNeotropic—Nearctic[5,7,10,16,17,18]
Myzus persicae (Sulzer, 1776)18–56 bPiercing–suckingGeneralistIndo-Malayan[5,7,10,16,17]
Smynthurodes betae Westwood, 184918–22; 32–56Piercing–suckingGeneralistUnknown[10,17]
Hemiptera: Triozidae
Heterotrioza chenopodii (Reuter, 1876) (=Trioza chenopodii Reuter)29–34Piercing–suckingSpecialistPalearctic[5,15,19]
Hemiptera: Pentatomidae
Nezara viridula (Linnaeus, 1758)18–56Piercing–suckingGeneralistUnknown[5,10,15]
Hemiptera: Lygaeidae
Nysius simulans (Stål, 1859)29–38Piercing–suckingGeneralistNeotropic[10]
Oncopeltus miles (Blanchard, 1852)19–40Piercing–suckingSpecialistChile[10,20]
Hemiptera: Coreidae
Leptoglossus chilensis (Spinola, 1852)26–44Piercing–suckingGeneralistNeotropic[5,15,21]
Hemiptera: Rhopalidae
Liorhyssus hyalinus (Fabricius, 1794)18–38Piercing–suckingGeneralistUnknown[10]
Liorhyssus lineatoventris (Spinola, 1852)30–40 bPiercing–suckingGeneralistNeotropic[22]
Hemiptera: Miridae
Orthotylus flavosparsus (Sahlberg, 1841)33–34 bPiercing–suckingGeneralistUnknown[5,15,22]
Thysanoptera: Thripidae
Frankliniella occidentalis (Pergande, 1895)18–44 b,cCell puncturingGeneralistNearctic[12,18]
Thrips tabaci Lindeman, 188918–40Cell puncturingGeneralistUnknown[7,10,16,18]
Diptera: Agromyzidae
Liriomyza huidobrensis Blanchard, 192618–49 a,b,cLeaf miningGeneralistNeotropic[5,7,10,16]
Coleoptera: Chrysomelidae
Epitrix sp.32–34 bChewingUnknownNeotropic—Nearctic[5,7,10,12,16]
Coleoptera: Curculionidae
Trichocyphus rubricollis (Blanchard, 1847)18–26 aChewingUnknownNeotropic[23]
Coleoptera: Meloidae
Pseudomeloe sp.19–22 aChewingUnknownNeotropic[7]
Lepidoptera: Coleophoridae
Coleophora versurella Zeller, 184932–40ChewingSpecialistNeotropic—Nearctic[11,24,25]
Lepidoptera: Crambidae
Achyra similalis (Guenée, 1854) (=Loxostege similalis (Guenée))18–40 bChewingSpecialistNeotropic—Nearctic[10,11,25]
Spoladea recurvalis (Fabricius, 1794)18–19ChewingSpecialistNeotropic[5,7,10]
Lepidoptera: Gelechiidae
Eurysacca media Povolný, 198632–34ChewingSpecialistNeotropic[11,26,27]
Eurysacca quinoae Povolný, 199719 aChewingSpecialistNeotropic[28]
Lepidoptera: Noctuidae
Agrotis experta (Walker, 1869) (=Feltia experta (Walker))18–26ChewingGeneralistNeotropic[5,7,10,16]
Agrotis ipsilon (Hufnagel, 1766)18–44 cChewingGeneralistUnknown[5,7,10,16]
Agrotis malefida (Guenée, 1852)32–56ChewingGeneralistNeotropic[7,10]
Copitarsia spp. (species complex)18–56 a,b,c,dChewingGeneralistNeotropic[5,10,11,12,16,29]
Chrysodeixis includens (Walker, 1858) (=Pseudoplusia includens (Walker)) (=Phytometra oo (Cramer))18–26ChewingGeneralistNeotropic—Nearctic[5,10,12]
Feltia subterranea (Fabricius, 1794) (=Agrotis subterranea)18–40 b,cChewingGeneralistNeotropic—Nearctic[5,10]
Helicoverpa atacamae Hardwick, 196518–41 aChewingGeneralistNeotropic[5,16,30]
Helicoverpa gelotopoeon (Dyar, 1921)18–40 aChewingGeneralistNeotropic[5,12,15,30]
Helicoverpa zea (Boddie, 1850)18–44ChewingGeneralistNeotropic—Nearctic[5,7,10,12,16,18]
Peridroma saucia (Hübner, 1808)18–56ChewingGeneralistUnknown[5,7,10,16]
Rachiplusia nu (Guenée, 1852)18–44ChewingGeneralistNeotropic—Nearctic[5,10,11,15]
Spodoptera eridania (Stoll, 1782)18–33ChewingGeneralistNeotropic—Nearctic[5,7,10,16]
Spodoptera frugiperda (J.E. Smith, 1797)18–22ChewingGeneralistNeotropic—Nearctic[5,7,10,15,16]
Spodoptera ochrea (Hampson, 1909)18–22ChewingGeneralistNeotropic[5,10]
Trichoplusia ni (Hübner, 1803)18–44 bChewingGeneralistUnknown[12,18]
Acari: Tetranychidae
Tetranychus urticae Koch, 183618–44 bCell puncturingGeneralistUnknown[5,10]
a Collected in this study in Tarapacá (19°24′ S, 68°35′ W); b Metropolitana (33°40′ S, 70°35′ W, or 33°29′ S, 70°36′ W); c O’Higgins (34°29′, 72°01′ W, or 34°15′ S, 71°47′ W); d Los Lagos (41°50′ S, 74°00′ W, or 42°00′ S, 73°53′ W).
Table
Table 2. Description of the clustering patterns of arthropod species associated with quinoa in Chile.
Table 2. Description of the clustering patterns of arthropod species associated with quinoa in Chile.
Cluster GroupGeographical Limits of Each Cluster (° S)Species Present within the Delimited Area *
117.5–25.832 species:Achyra similalis, Agrotis experta, Agrotis ipsilon, Anacuerna centrolinea, Aphis craccivora, Aphis gossypii, Chrysodeixis includens, Copitarsia spp., Eurysacca quinoae, Feltia subterranea, Frankliniella occidentalis, Helicoverpa atacamae, Helicoverpa gelotopoeon, Helicoverpa zea, Liorhyssus hialinus, Liriomyza huidobrensis, Macrosiphum euphorbiae, Myzus persicae, Nezara viridula, Oncopeltus miles, Peridroma saucia, Pseudomeloe sp., Rachiplusia nu, Smynthurodes betae, Spodoptera eridania, Spodoptera frugiperda, Spodoptera ochrea, Spoladea recurvalis, Tetranychus urticae, Thrips tabaci, Trichocyphus rubricollis, Trichoplusia ni
225.9—32.027 species:Achyra similalis, Agrotis ipsilon, Aphis craccivora, Aphis gossypii, Copitarsia spp., Dichroplus maculipennis, Feltia subterranea, Frankliniella occidentalis, Helicoverpa atacamae, Helicoverpa gelotopoeon, Helicoverpa zea, Heterotrioza chenopodii, Leptoglossus chilensis, Liorhyssus hialinus, Liorhyssus lineatoventris, Liriomyza huidobrensis, Macrosiphum euphorbiae, Myzus persicae, Nezara viridula, Nysius simulans, Oncopeltus miles, Peridroma saucia, Rachiplusia nu, Spodoptera eridania, Tetranychus urticae, Thrips tabaci, Trichoplusia ni
332.1—39.534 species:Achyra similalis, Agrotis ipsilon, Agrotis malefida, Aphis craccivora, Aphis gossypii, Coleophora versurella, Copitarsia spp., Dichroplus maculipennis, Epitrix sp., Eurysacca media, Feltia subterranea, Frankliniella occidentalis, Helicoverpa atacamae, Helicoverpa gelotopoeon, Helicoverpa zea, Heterotrioza chenopodii, Leptoglossus chilensis, Liorhyssus hialinus, Liorhyssus lineatoventris, Liriomyza huidobrensis, Macrosiphum euphorbiae, Myzus persicae, Nezara viridula, Nysius simulans, Oncopeltus miles, Orthotylus flavosparsus, Paratanus exitiosus, Peridroma saucia, Rachiplusia nu, Smynthurodes betae, Spodoptera eridania, Tetranychus urticae, Thrips tabaci, Trichoplusia ni
439.5—43.722 species:Achyra similalis, Agrotis ipsilon, Agrotis malefida, Aphis craccivora, Aphis gossypii, Copitarsia spp., Dichroplus maculipennis, Frankliniella occidentalis, Helicoverpa atacamae, Helicoverpa zea, Leptoglossus chilensis, Liorhyssus lineatoventris, Liriomyza huidobrensis, Macrosiphum euphorbiae, Myzus persicae, Nezara viridula, Paratanus exitiosus, Peridroma saucia, Rachiplusia nu, Smynthurodes betae, Tetranychus urticae, Trichoplusia ni
* For information regarding species-specific distribution within each cluster, see Table 1.
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Chorbadjian, R.A.; Ahumada, M.I.; Urra, F.; Elgueta, M.; Gilligan, T.M. Biogeographical Patterns of Herbivore Arthropods Associated with Chenopodium quinoa Grown along the Latitudinal Gradient of Chile. Plants 2021, 10, 2811. https://doi.org/10.3390/plants10122811

AMA Style

Chorbadjian RA, Ahumada MI, Urra F, Elgueta M, Gilligan TM. Biogeographical Patterns of Herbivore Arthropods Associated with Chenopodium quinoa Grown along the Latitudinal Gradient of Chile. Plants. 2021; 10(12):2811. https://doi.org/10.3390/plants10122811

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Chorbadjian, Rodrigo A., María I. Ahumada, Francisco Urra, Mario Elgueta, and Todd M. Gilligan. 2021. "Biogeographical Patterns of Herbivore Arthropods Associated with Chenopodium quinoa Grown along the Latitudinal Gradient of Chile" Plants 10, no. 12: 2811. https://doi.org/10.3390/plants10122811

APA Style

Chorbadjian, R. A., Ahumada, M. I., Urra, F., Elgueta, M., & Gilligan, T. M. (2021). Biogeographical Patterns of Herbivore Arthropods Associated with Chenopodium quinoa Grown along the Latitudinal Gradient of Chile. Plants, 10(12), 2811. https://doi.org/10.3390/plants10122811

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