Description of three new species of Geometridae (Lepidoptera) using species delimitation in an integrative taxonomy approach for a cryptic species complex

Abstract

The genus Eois Hbner (Geometridae: Larentiinae) comprises 254 valid species, 217 of which were described from the Neotropics and 31 of those having their type locality in Brazil. Since this species rich genus has never been revised, and may potentially include many cryptic undescribed species, Eois embodies a problematic taxonomic scenario. The actual diversity of Eois is greatly underestimated and the Brazilian fauna is poorly known, both because of inadequate sampling and because of the potential existence of cryptic species "hidden" within some nominal taxa. In this study we investigated the diversity within a cryptic species complexes associated to the E. pallidicosta and E. odatis clades. We describe three new species Eois oya Moraes & Montebello sp. nov., Eois ewa Moraes & Stanton sp. nov., and Eois oxum Moraes & Freitas sp. nov., in an integrative taxonomy approach, using morphology, host plant use and species delimitation tools.

Introduction

Geometridae is a megadiverse family with over 24,000 species, being the most species rich lineage in the superfamily Geometroidea and the second most species-rich family among Macroheterocera lineages (Scoble, 1999; Sihvonen et al., 2011; Mitter, Davis & Cummings, 2017). The family Geometridae represents a challenge for researchers because of the taxonomic uncertainties around some species-rich genera, for which taxonomic reviews are lacking and several new taxa await formal descriptions (Strutzenberger et al., 2011; Strutzenberger, Brehm & Fiedler, 2012). Despite the existence of a worldwide catalog (Scoble, 1999), only a small subset of Geometridae genera has been revised (Hulst, 1896; Wehrli, 1939; Rindge, 1990, Pitkin, 2002). Most of these taxonomic studies are restricted to specific geographic areas, leaving the Neotropics as one of the least studied biogeographic regions for the Geometridae fauna.

Eois Hbner belongs to the subfamily Larentiinae and is one of the most species-rich genus, with 254 described species (Brehm et al., 2011), 217 of which were described for the Neotropical region and 31 primary types for Brazil. Species of Eois are small, reaching up to 2 cm in wingspan, and most species present a wing pattern consisting of a yellowish or brown background patterned with reddish or rusty symmetrical bands on both wings. Based on a study with some species from Borneo (Holloway, 1997), the male genitalia lack the uncus and labides, while female genitalia present a robust bursa with multiseriate signa. Recently, Brehm et al. (2011) showed that characters from valvae and vesica on the male genitalia might be phylogenetically informative and also useful in delimiting species.

Notwithstanding Eois being recognized as an important component of the diversity of neotropical moths (Brehm et al., 2011), there is still a large gap in the knowledge and representativeness of the Brazilian fauna. Single-locus species delimitation methods were recognized as a useful approach when working with montane Eois species (Strutzenberger et al., 2011) and recently this diversity was also increased for lowland species (Moraes et al., 2021). However, despite the use of molecular methods for species-delimitation having proven to be extremely valuable in highlighting cryptic diversity, fewer than 30% of the studies on species delimitation made taxonomic recommendations and only 25% described new species (Carstens et al., 2013).

In the present study we contribute to the knowledge of Eois diversity using an integrative taxonomic approach on cryptic species complexes, and describe three new species of Eois. Accordingly, we accessed the molecular diversity and used the Automatic Barcode Gap Discovery method (ABGD) for species delimitation (Puillandre et al., 2012). To test the validity of the molecular taxonomic units (MOTUs) we studied morphological characters for wing pattern and genitalia, as well as host plant use by larvae. We expect that these practices will improve the number of new taxa described in cryptic complexes, increasing the knowledge on the real diversity of Eois from Brazil.

Materials and Methods

Sampling

Immature stages and imagos of Eois were obtained from six localities: (i) Serra do Japi Biological Reserve (23 14 S 46 58 W), Jundia, So Paulo, Brazil; (ii) Boraceia Biological Station (23 39 S 45 54 W), Salespolis, So Paulo, Brazil; (iii) Intervales State Park (24 16 S 48 24 W), Ribeiro Grande, So Paulo, Brazil, (iv) Itatiaia National Park (22 27 S 44 37 W), Itatiaia, Rio de Janeiro, Brazil, (v) Serra dos Orgos National Park (22 27 S 42 59 W), Terespolis, Rio de Janeiro, Brazil, and (vi) Adolpho Ducke Forest Reserve (2 57 S 59 55 W), Manaus, Amazonas, Brazil.

Imagos were collected during the night using a light source consisting of a a 500 W mix bulb on a square white sheet (2 m side). Immatures were collected by searching plants of the genus Piper L. and Peperomia Ruiz & Pav.(Piperaceae), known larval host plants of several species of Eois, and were reared in the laboratory. Samples of the host plant, including leaves, inflorescence and fruits, were also collected for further identification. Permits for field trips were issued by Instituto Chico Mendes de Conservao da Biodiversidade (ICMBio, permit nos. 10362-1, 15780-10 and 22205-6). All new described species are registered in the SISGEN (A4ED092).

Rearing methods

Larvae were reared in individual 300 mL clear plastic vials with lids, and provided with leaves of the same Piper and Peperomia plants on which they were collected (Moraes, Otero & Freitas, 2017). Pupae were transferred to individual 50 mL clear plastic vials with lids and moist cotton wool until emergence. Larvae and pupae were maintained under constant temperature (25 C) and 12 h light: 12 h dark cycle. After emergence, imagos were sacrificed for DNA extraction and genitalia dissection. Samples of the host plants were collected and compared to previously identified samples from the same locality made at the Laboratrio de Qumica de Produtos Naturais, at the University of So Paulo, and compared to the species description in the Brazilian Flora 2020 project (Guimares, Queiroz & Medeiros, 2020).

DNA extraction and PCR conditions

Three legs were removed from each specimen shortly after collection and before spreading. Sampled legs were preserved dry and stored in 1.5 mL tubes at 20 C. Total genomic DNA was extracted with DNeasy Blood & Tissue Kit (Qiagen, Venlo, Netherlands), according to the manufacturers protocol with final elution in 100 l elution buffer. The 5 end (barcode region) of the mitochondrial gene cytochrome oxidase subunit I (COI, 650 bp) was amplified using the primers HCO and LCO (Folmer et al., 1994) containing the T3 and T7 promotor universal tails, respectively (Wahlberg & Wheat, 2008). Polymerase chain reactions (PCRs) were performed with 13 l total volume containing 12 l of extracted DNA, 3.24.2 l of H₂O milli-Q, 6.5 l of 2x MyTaq HS red mix (Bioline Co., London, UK), and 0.65 l of each primer (10 mM). PCR products were amplified as follows: 96 C for 7 min, followed by 40 cycles of 96 C for 30 s, 50 C for 30 s and 72 C for 90 s, and a final extension period of 72 C for 10 min.

Amplicons were purified adding a mix of 1.3 l of FastAP Thermosensitive Alkaline Phosphatase (Thermofisher Scientific, Waltham, MA, USA) and 0.7 l of Exonuclease 1 (Thermofisher Scientific, Waltham, MA, USA) to 10 l of PCR products. Purified products were sent for Sanger sequencing.

Alignment, tree inference and species delimitation

The genetic dataset consisted of 160 newly sequenced individuals of 18 putative species combined with 36 sequences obtained from Genbank (Table 1). Sequences were aligned using MAFFT (Katoh et al., 2002) implemented in Geneious v.11.0.2 (Kearse et al., 2012). The alignments were carefully checked by eye, taking into consideration the reading frame relative to the reference sequence. The Maximum Likelihood analyses were conducted using RAxML-HPC2 V.8.2.10 (Stamatakis, 2014) on the webserver CIPRES Science Gateway (Miller, Pfeiffer & Schwartz, 2010). Support for nodes was evaluated with 1000 ultrafast bootstrap (UFBoot2) approximations (Hoang et al., 2018), UFBoot2 values 95 indicate well-supported clades.

Table 1. List of specimens vouchered, the associated clade, geographical localities, host plant and herbarium voucher for host plants used in this study.

GenBank Voucher	Clade	Locality	Host Plant	Herbarium Voucher
LEPSM818
LEPSM609
K2422-1	olivacea	Brazil, MS, Aquidauana	Piper tuberculatum Jacq.	K2422
K2422-1a	olivacea	Brazil, MS, Aquidauana	Piper tuberculatum Jacq.	K2422
K2426-2	olivacea	Brazil, MS, Aquidauana	Piper tuberculatum Jacq.	K2422
K2426-3	olivacea	Brazil, MS, Aquidauana	Piper tuberculatum Jacq.	K2422
M097-1	russearia	Brazil, SP, Mogi-Guau, Reserva Biolgica de Mogi-Guau	Piper arboreum Aubl.	K1953*
Mogi#906	russearia	Brazil, SP, Mogi-Guau, Reserva Biolgica de Mogi-Guau	Piper arboreum Aubl.	K1953*
M081-1	russearia	Brazil, SP, Mogi-Guau, Reserva Biolgica de Mogi-Guau	Piper crassinervium Kunth.	K1954*
Mogi#802	russearia	Brazil, SP, Mogi-Guau, Reserva Biolgica de Mogi-Guau	Piper crassinervium Kunth.	K1954*
M076-1	russearia	Brazil, SP, Mogi-Guau, Reserva Biolgica de Mogi-Guau	Piper crassinervium Kunth.	K1954*
M081-2	russearia	Brazil, SP, Mogi-Guau, Reserva Biolgica de Mogi-Guau	Piper crassinervium Kunth.	K1954*
Mogi#818	russearia	Brazil, SP, Mogi-Guau, Reserva Biolgica de Mogi-Guau	Piper crassinervium Kunth.	K1954*
K2411-2	russearia	Brazil, MS, Aquidauana	Piper sp 2	K2417
K2417-12	russearia	Brazil, MS, Aquidauana	Piper sp 2	K2417
K2417-7	russearia	Brazil, MS, Aquidauana	Piper sp 2	K2417
K2417-27	russearia	Brazil, MS, Aquidauana	Piper sp 2	K2417
K2416-16	russearia	Brazil, MS, Aquidauana	Piper sp 2	K2417
LEPSM906	adimaria
LEPSM907	adimaria
K2206-1	odatis	Brazil, SP, Jundia, Reserva Biolgica da Serra do Japi	Piper lindbergii C.DC	K2493
K2325-15	odatis	Brazil, SP, Jundia, Reserva Biolgica da Serra do Japi	Piper lindbergii C.DC	K2493
K2325-9	odatis	Brazil, SP, Jundia, Reserva Biolgica da Serra do Japi	Piper lindbergii C.DC	K2493
K2325-16	odatis	Brazil, SP, Jundia, Reserva Biolgica da Serra do Japi	Piper lindbergii C.DC	K2493
K2325-10	odatis	Brazil, SP, Jundia, Reserva Biolgica da Serra do Japi	Piper lindbergii C.DC	K2493
K2206-23	odatis	Brazil, SP, Jundia, Reserva Biolgica da Serra do Japi	Piper lindbergii C.DC	K2493
M768-1	odatis	Brazil, SP, Jundia, Reserva Biolgica da Serra do Japi	Piper lindbergii C.DC	M1033
M528-4	odatis	Brazil, RJ, Itatiaia, Parque Nacional do Itatiaia	Piper amplumKunth.	M1033
M528-1	odatis	Brazil, RJ, Itatiaia, Parque Nacional do Itatiaia	Piper amplum Kunth.	M1033
LEPSM909	odatis
K2325-2	odatis	Brazil, SP, Jundia, Reserva Biolgica da Serra do Japi	Piper lindbergii C.DC	K2493
K2452-1	odatis	Brazil, RJ, Itatiaia, Parque Nacional do Itatiaia	Peperomia hispidula (Sw.) A. Dietr.	K1612*
K2452-4	odatis	Brazil, RJ, Itatiaia, Parque Nacional do Itatiaia	Peperomia hispidula (Sw.) A. Dietr.	K1612*
K2452-5	odatis	Brazil, RJ, Itatiaia, Parque Nacional do Itatiaia	Peperomia hispidula (Sw.) A. Dietr.	K1612*
K2452-2	odatis	Brazil, RJ, Itatiaia, Parque Nacional do Itatiaia	Peperomia hispidula (Sw.) A. Dietr.	K1612*
M624-1	odatis	Brazil, RJ, Itatiaia, Parque Nacional do Itatiaia	Piper malacophyllum C. Presl	M1038
M289-1	odatis	Brazil, SP, So Paulo, Parque Estadual do Jaragu	Piper malacophyllum C. Presl	K2294*
#107	odatis
M621-1	odatis	Brazil, RJ, Itatiaia, Parque Nacional do Itatiaia	Piper malacophyllum C. Presl	M1038
M436-1	odatis	Brazil, SP, So Paulo, Parque Estadual do Jaragu	Piper malacophyllum C. Presl	K2294*
K2159-7	odatis	Brazil, RJ, Itatiaia, Parque Nacional do Itatiaia	Piper malacophyllum C. Presl	K2159
M576-1	odatis	Brazil, RJ, Itatiaia, Parque Nacional do Itatiaia	Piper malacophyllum C. Presl	M1038
M657-1	odatis	Brazil, SP, So Paulo, Parque Estadual do Jaragu	Piper gaudichaudianum Kunth.	K2311*
M435-1	odatis	Brazil, SP, So Paulo, Parque Estadual do Jaragu	Piper malacophyllum C. Presl	K2294*
M622-1	odatis	Brazil, RJ, Itatiaia, Parque Nacional do Itatiaia	Piper malacophyllum C. Presl	M1038
M388-1	odatis	Brazil, SP, So Paulo, Parque Estadual do Jaragu	Piper gaudichaudianum Kunth.	K2311*
K2157-2	odatis	Brazil, RJ, Itatiaia, Parque Nacional do Itatiaia	Piper malacophyllum C. Presl	K2165
PPU721	odatis	Brazil, SP, Jundia, Reserva Biolgica da Serra do Japi	Piper malacophyllum C. Presl	K2306
M761-1	odatis	Brazil, SP, Jundia, Reserva Biolgica da Serra do Japi	Piper gaudichaudianum Kunth.	K2198*
M754-1	odatis	Brazil, SP, Jundia, Reserva Biolgica da Serra do Japi	Piper gaudichaudianum Kunth.	K2198*
PPU660	odatis	Brazil, SP, Jundia, Reserva Biolgica da Serra do Japi	Piper malacophyllum C. Presl	K2306
M358-1	odatis	Brazil, SP, So Paulo, Parque Estadual do Jaragu	Piper cubataonum C. DC	K1951*
M775-1	odatis	Brazil, SP, Jundia, Reserva Biolgica da Serra do Japi	Piper gaudichaudianum Kunth.	K2198*
M678-1	odatis	Brazil, SP, So Paulo, Parque Estadual do Jaragu	Piper malacophyllum C. Presl	K2294*
M677-1	odatis	Brazil, SP, So Paulo, Parque Estadual do Jaragu	Piper gaudichaudianum Kunth.	K2311*
K2165-3	odatis	Brazil, RJ, Itatiaia, Parque Nacional do Itatiaia	Piper malacophyllum C. Presl	K2165
M514-1	odatis	Brazil, RJ, Itatiaia, Parque Nacional do Itatiaia	Piper crassinervium Kunth.	K1954*
K2423-5	odatis	Brazil, MS, Corumb	Piper amalago L.	K2421
K2423-4	odatis	Brazil, MS, Corumb	Piper amalago L.	K2421
K2423-8	odatis	Brazil, MS, Corumb	Piper amalago L.	K2421
K2423-3	odatis	Brazil, MS, Corumb	Piper amalago L.	K2421
K2212-11	odatis	Brazil, SP, Jundia, Reserva Biolgica da Serra do Japi	Piper malacophyllum C. Presl	K2212
M616-1	odatis	Brazil, RJ, Itatiaia, Parque Nacional do Itatiaia	Piper chimonanthifolium Kunth.	K1960*
M399-1	odatis	Brazil, SP, So Paulo, Parque Estadual do Jaragu	Piper malacophyllum C. Presl	K2294*
#359	odatis
M731-1	odatis	Brazil, SP, Jundia, Reserva Biolgica da Serra do Japi	Piper chimonanthifolium Kunth.	K1960*
K2454-38	odatis	Brazil, SP, Campos do Jordo	Piper gaudichaudianum Kunth.	K2446
K2454-31	odatis	Brazil, SP, Campos do Jordo	Piper gaudichaudianum Kunth.	K2446
K2446-7	odatis	Brazil, SP, Campos do Jordo	Piper gaudichaudianum Kunth.	K2446
K2454-47	odatis	Brazil, SP, Campos do Jordo	Piper gaudichaudianum Kunth.	K2446
K2453-47	odatis	Brazil, SP, Campos do Jordo	Piper gaudichaudianum Kunth.	K2446
K2165-5	odatis	Brazil, RJ, Itatiaia, Parque Nacional do Itatiaia	Piper malacophyllum C. Presl	K2165
M611-1	odatis	Brazil, RJ, Itatiaia, Parque Nacional do Itatiaia	Piper chimonanthifolium Kunth.	K1960*
#845	odatis	Brazil, SP, Mogi-Guau, Reserva Biolgica de Mogi-Guau	Piper gaudichaudianum Kunth.
#855	odatis	Brazil, SP, Mogi-Guau, Reserva Biolgica de Mogi-Guau	Piper gaudichaudianum Kunth.
#841	odatis	Brazil, SP, Mogi-Guau, Reserva Biolgica de Mogi-Guau	Piper gaudichaudianum Kunth.
PPU651	odatis	Brazil, SP, Jundia, Reserva Biolgica da Serra do Japi	Piper hillianum C. DC.	K1920*
M844-2	odatis	Brazil, SP, Capo Bonito, Parque Estadual Intervales	Piper gaudichaudianum Kunth.	M1034
M617-1	odatis	Brazil, RJ, Itatiaia, Parque Nacional do Itatiaia	Piper chimonanthifolium Kunth.	K1960*
M735-1	odatis	Brazil, SP, Jundia, Reserva Biolgica da Serra do Japi	Piper chimonanthifolium Kunth.	K2495
M738-1	odatis	Brazil, SP, Jundia, Reserva Biolgica da Serra do Japi	Piper chimonanthifolium Kunth.	K2495
M618-1	odatis	Brazil, RJ, Itatiaia, Parque Nacional do Itatiaia	Piper chimonanthifolium Kunth.	K1960*
M573-1-4	odatis	Brazil, RJ, Itatiaia, Parque Nacional do Itatiaia	Piper chimonanthifolium Kunth.	K1960*
M573-1-3	odatis	Brazil, RJ, Itatiaia, Parque Nacional do Itatiaia	Piper chimonanthifolium Kunth.	K1960*
K2453-4-1	odatis	Brazil, SP, Campos do Jordo	Piper gaudichaudianum Kunth.	K2446
M573-1-5	odatis	Brazil, RJ, Itatiaia, Parque Nacional do Itatiaia	Piper chimonanthifolium Kunth.	K1960*
M163-1-1	odatis	Brazil, RJ, Itatiaia, Parque Nacional do Itatiaia	Piper chimonanthifolium Kunth.	K1960*
K2453-4b	odatis	Brazil, SP, Campos do Jordo	Piper gaudichaudianum Kunth.	K2446
K2453-4-2	odatis	Brazil, SP, Campos do Jordo	Piper gaudichaudianum Kunth.	K2446
K2453-4	odatis	Brazil, SP, Campos do Jordo	Piper gaudichaudianum Kunth.	K2446
M573-1-2	odatis	Brazil, RJ, Itatiaia, Parque Nacional do Itatiaia	Piper chimonanthifolium Kunth.	K1960*
K2453-4-3	odatis	Brazil, SP, Campos do Jordo	Piper gaudichaudianum Kunth.	K2446
LEPSM920
#25
M022-1	veniliata	Brazil, SP, So Paulo, Parque Estadual do Jaragu	Piper gaudichaudianum Kunth.	K2494*
M286-1	veniliata	Brazil, SP, So Paulo, Parque Estadual do Jaragu	Piper gaudichaudianum Kunth.	K2494*
K2326-1	veniliata	Brazil, SP, Jundia, Reserva Biolgica da Serra do Japi	Piper gaudichaudianum Kunth.	K2494*
K2322-1	hyperythraria	Brazil, SP, Jundia, Reserva Biolgica da Serra do Japi	Piper arboreum Aubl.	K1953*
M522-3	hyperythraria	Brazil, RJ, Itatiaia, Parque Nacional do Itatiaia	Piper cernuum Vell.	K1925*
K2322-5	hyperythraria	Brazil, SP, Jundia, Reserva Biolgica da Serra do Japi	Piper arboreum Aubl.	K1953*
LEPSM1094	hyperythraria
K2322-17	hyperythraria	Brazil, SP, Jundia, Reserva Biolgica da Serra do Japi	Piper arboreum Aubl.	K1953*
#798	hyperythraria	Brazil, SP, Mogi-Guau, Reserva Biolgica de Mogi-Guau	Piper arboreum Aubl.	K1953*
M589-3	hyperythraria	Brazil, RJ, Itatiaia, Parque Nacional do Itatiaia	Piper arboreum Aubl.	K1953*
M644-2a	hyperythraria	Brazil, RJ, Itatiaia, Parque Nacional do Itatiaia	Piper arboreum Aubl.	K1953*
M591-1	hyperythraria	Brazil, RJ, Itatiaia, Parque Nacional do Itatiaia	Piper truncatum Vell.	K1950*
LEPSM901	hyperythraria
K2366-1	olivacea	Brazil, SP, Capo Bonito, Parque Estadual Intervales	Piper aduncum L.	K2387
K2369-1	olivacea	Brazil, SP, Capo Bonito, Parque Estadual Intervales	Piper aduncum L.	K2387
K2369-3	olivacea	Brazil, SP, Capo Bonito, Parque Estadual Intervales	Piper aduncum L.	K2387
M523-2	olivacea	Brazil, RJ, Itatiaia, Parque Nacional do Itatiaia	Piper cernuum Vell.	K1925*
LEPSM615	olivacea
M527-4	olivacea	Brazil, RJ, Itatiaia, Parque Nacional do Itatiaia	Piper cernuum Vell.	K1925*
M572-2	olivacea	Brazil, RJ, Itatiaia, Parque Nacional do Itatiaia	Piper cernuum Vell.	K1925*
LEPSM618	olivacea
M516-1	olivacea	Brazil, RJ, Itatiaia, Parque Nacional do Itatiaia	Piper crassinervium Kunth.	K1954*
K2423-2	olivacea	Brazil, MS, Corumb	Piper amalago L.	K2423
M544-1	olivacea	Brazil, RJ, Itatiaia, Parque Nacional do Itatiaia	Piper crassinervium Kunth.	K1954*
K2367-3	olivacea	Brazil, SP, Capo Bonito, Parque Estadual Intervales	Piper crassinervium Kunth.	K1954*
K2372-10	olivacea	Brazil, SP, Capo Bonito, Parque Estadual Intervales	Piper crassinervium Kunth.	K1954*
K2367-5	olivacea	Brazil, SP, Capo Bonito, Parque Estadual Intervales	Piper crassinervium Kunth.	K1954*
K2322-2	olivacea	Brazil, SP, Jundia, Reserva Biolgica da Serra do Japi	Piper arboreum Aubl.	K1953*
K2372-6	olivacea	Brazil, SP, Capo Bonito, Parque Estadual de Intervales	Piper crassinervium Kunth.	K1954*
K2372-8	olivacea	Brazil, SP, Capo Bonito, Parque Estadual Intervales	Piper crassinervium Kunth.	K1954*
#862	olivacea	Brazil, SP, Mogi-Guau, Reserva Biolgica de Mogi-Guau	Piper crassinervium Kunth.
M551-2	olivacea	Brazil, RJ, Itatiaia, Parque Nacional do Itatiaia	Piper crassinervium Kunth.	K1954*
M548-1	olivacea	Brazil, RJ, Itatiaia, Parque Nacional do Itatiaia	Piper crassinervium Kunth.	K1954*
M626-1	olivacea	Brazil, RJ, Itatiaia, Parque Nacional do Itatiaia	Piper crassinervium Kunth.	K1954*
M593-1	olivacea	Brazil, RJ, Itatiaia, Parque Nacional do Itatiaia	Piper cf. tectoniifolium Kunth.	K1958*
K1228-2	olivacea	Colombia, Bogota	Piper bogotense C. DC.
JQ424371.1	pallidicosta
JQ424372.1	pallidicosta
K1228-1	pallidicosta	Colombia, Bogota	Piper bogotense C. DC.
JQ179873.1	pallidicosta
JF859258.1	pallidicosta
JQ424375.1	pallidicosta
GQ433544.1	pallidicosta
KU381316.1	pallidicosta
JQ179915.1	pallidicosta
MG572804.1	pallidicosta
JQ179875.1	pallidicosta
JQ179870.1	pallidicosta
KU381055.1	pallidicosta
HQ576249.1	pallidicosta
MG572805.1	pallidicosta
JX150931.1	pallidicosta
KU381753.1	pallidicosta
JX150863.1	pallidicosta
GQ433565	pallidicosta
GQ433565.1	pallidicosta
JQ179924.1	pallidicosta
MG572814.1	pallidicosta
JQ179903.1	pallidicosta
JQ179880.1	pallidicosta
GQ433564.1	pallidicosta
JQ424379.1	pallidicosta
JQ424374.1	pallidicosta
M157-3	pallidicosta	Brazil, RJ, Itatiaia, Parque Nacional do Itatiaia	Piper reitzii Yunck.	M157
LEPSM922	pallidicosta
M156-5	pallidicosta	Brazil, RJ, Itatiaia, Parque Nacional do Itatiaia	Piper reitzii Yunck.	M156
M155-12	pallidicosta	Brazil, RJ, Itatiaia, Parque Nacional do Itatiaia	Piper reitzii Yunck.	M158
M155-3	pallidicosta	Brazil, RJ, Itatiaia, Parque Nacional do Itatiaia	Piper reitzii Yunck.	M158
JQ179895.1	pallidicosta
JQ179923.1	pallidicosta
JQ179901.1	pallidicosta
JQ179902.1	pallidicosta
JQ179905.1	pallidicosta
JQ179906.1	pallidicosta
GQ433557.1	pallidicosta
JQ179891.1	pallidicosta
JQ179941.1	pallidicosta
M594-1	olivacea	Brazil, RJ, Itatiaia, Parque Nacional do Itatiaia	Piper cubataonum C DC.	K1951*
M357-2	olivacea	Brazil, SP, So Paulo, Parque Estadual do Jaragu	Piper cubataonum C DC.	K1951*
M595-1	olivacea	Brazil, RJ, Itatiaia, Parque Nacional do Itatiaia	Piper cubataonum C DC.	K1951*
M594-2	olivacea	Brazil, RJ, Itatiaia, Parque Nacional do Itatiaia	Piper cubataonum C DC.	K1951*
K2420-27	russearia	Brazil, MS, Aquidauana	Piper sp 1	K2420
K2420-3	russearia	Brazil, MS, Aquidauana	Piper sp 1	K2420
K2420-21	russearia	Brazil, MS, Aquidauana	Piper sp 1	K2420
K2420-a	russearia	Brazil, MS, Aquidauana	Piper sp 1	K2420
TMD2018#4	russearia	Brazil, AM, Manaus, Reserva Florestal Adolpho Ducke	Piper erectipilum Yunck.	M1041
TMD2018#5	russearia	Brazil, AM, Manaus, Reserva Florestal Adolpho Ducke	Piper erectipilum Yunck.	M1041
TMD2018#6	russearia	Brazil, AM, Manaus, Reserva Florestal Adolpho Ducke	Piper erectipilum Yunck.	M1041
TMD2018#9	russearia	Brazil, AM, Manaus, Reserva Florestal Adolpho Ducke	Piper erectipilum Yunck.	M1041
TMD2018#12	russearia	Brazil, AM, Manaus, Reserva Florestal Adolpho Ducke	Piper erectipilum Yunck.	M1041
TMD2018#20	russearia	Brazil, AM, Manaus, Reserva Florestal Adolpho Ducke	Piper erectipilum Yunck.	M1041

Note:

Herbarium specimens that were identified by comparison to previously collected samples deposited at the University of So Paulo Herbarium (SPF) are reported with (*).

In order to study the species boundaries within our dataset, we used a species delimitation method focused on single-locus gene analysis: The Automatic Barcode Gap Discovery (ABGD, Puillandre et al., 2012). This method appeared to be more congruent with the Eois morphology compared to other methods (mPTP and bPTP) (Moraes et al., 2021). The ABGD method seeks to quantify a range of the barcode gap that separates intra from interspecific distances, automatically clustering sequences into candidate species based on pairwise distances (Puillandre et al., 2012). Default settings were used for the prior range for maximum intraspecific divergence (0.001, 0.1). Results were compared using Jukes-Cantor (JC69) corrected distances and relative gap width of 1.0. ABGD analyses were performed using the graphic web version (https://bioinfo.mnhn.fr/abi/public/abgd/).

Morphological study

The external morphology and color pattern were analyzed following the usual protocols (Winter, 2000). Wing venation and pattern were recorded and genitalia of females and males were dissected. For interpretation and descriptions of genital structures we followed the procedures outlined in Moraes & Duarte (2009), based on classical studies on Lepidoptera morphology (male genitalia in Pierce, 1909, Sibatani et al., 1954; Okagaki et al., 1955; Klots, 1956; Ogata et al., 1957; Birket-Smith, 1974; female genitalia in Pierce, 1914; Klots, 1956; Mutuura, 1972; Galicia, Snchez & Cordeiro, 2008).

A total of 11 specimens belonging to the three new species here described were examined. Characters of wing venation, color pattern, and male and female genitalia were analyzed. The genitalia were illustrated with a camera lucida attached to a stereomicroscope.

Acronyms for the collections are: MZUSPMuseu de Zoologia da Universidade de So Paulo, So Paulo, So Paulo, Brazil; ZUECZoological Collection of the Museu da Biodiversidade da Universidade Estadual de Campinas, Campinas, So Paulo, Brazil.

The electronic version of this article in Portable Document Format (PDF) will represent a published work according to the International Commission on Zoological Nomenclature (ICZN), and hence the new names contained in the electronic version are effectively published under that Code from the electronic edition alone. This published work and the nomenclatural acts it contains have been registered in ZooBank, the online registration system for the ICZN. The ZooBank LSIDs (Life Science Identifiers) can be resolved and the associated information viewed through any standard web browser by appending the LSID to the prefix http://zoobank.org/. The LSID for this publication is: urn:lsid:zoobank.org:pub:9450BCDC-7EB9-4CA6-BC76-04324F81ACA4. The online version of this work is archived and available from the following digital repositories: PeerJ, PubMed Central and CLOCKSS.

Results

Based on the present taxonomic sampling, the ML tree appeared divided into 10 main clades named after representative species names in each clade (Fig. 1), following Strutzenberger et al. (2017). From all defined MOTUs, three of them were identified as undescribed species based on present molecular results and also on available morphological evidence, and are here described. All but one species of Eois were reared on species of Piper and the host plant species in which larvae of each MOTU were collected are shown, when available (Fig. 1). The ABGD method used for delimiting species recovered each of new species here described as a distinct molecular operational taxonomic units (MOTUs).

Figure 1. Gene tree for COI-begin marker.

Colored leaves represent host plants for clades where adult representatives were obtained from reared immatures. Numbers on the node represent bootstrap stability equal or above 96%. Photographs by Simeo Moraes and Mariana Stanton.

The first undescribed species was identified in the larger clade named pallidicosta clade (after Eois pallidicosta (Warren, 1907)); the high UFBoot2 support values and the long branch length (related to a genetic distance higher than 3% from all other species in the clade) suggested that this is a distinct evolutionary lineage (Fig. 1).

The second undescribed species was identified in the odatis clade (named after Eois odatis (Druce, 1892)). In this clade, one MOTU was recovered based on four specimens forming a well supported clade that stands out by using Peperomia hispidula (Sw.) A.Dietr. (Piperaceae) as larval host plant.

The third undescribed species is part of the hyperythraria clade (named after Eois hyperythraria (Guene, 1858)) and is represented by a single individual collected a light source in a high montane area in Southeastern Brazil. Despite having returned to the sampling site several times no additional individuals were collected. Even though, its idiosyncratic wing pattern and the morphology of genitalia justifies the description of this new taxa based only on the holotype.

Species Description

Eois oya Moraes & Montebello sp.nov. (Figs. 2A2B, 3)

Figure 2. Habitus of Eois holotype specimens.

AB. Male, holotype of Eois oya sp.nov. A. Dorsal view. B. Ventral view. CD. Male, holotype of Eois ewa sp.nov. C., Dorsal view. D. Ventral view. EF. Female, holotype of Eois oxum sp.nov. Scale bar 1 cm. Photographs by Simeo Moraes.

Figure 3. Male and female genitalia of Eois oya sp.nov. paratype.

A. Male genitalia, genital capsule, dorsal view. B. Male genitalia, genital capsule, ventral view C. Male genitalia, genital capsule, lateral view. D. Male genitalia, aedeagus, lateral view. E. Female genitalia, dorsal view. Line drawings by Simeo Moraes and Ygor Montebello

Diagnosis ( and ). Forewing dorsal view with a horizontal black stripe on the trunk of Cu vein, from the base of wing reaching the outer margin. Forewing and hindwing with a black dot on the discal cell closure. Aedeagus with a pointed spine close to vesica, vesica bilobed with spiniform cornuti (Fig. 3D).

Description () (Figs. 2A2B). Head: Light brown. Frons light brown, vertex light brown. Labial palp light brown. Thorax: Predominantly light brown. Prothoracic collar with iridescent gold scales. Tegulae light brown. Forewing background light brown, darker proximally; horizontal black stripe on the trunk of Cu vein, from the base of wing reaching the outer margin; one black dot on the discal cell closure; two vertical, mirrored stripes beyond discal cell closure, from costal margin to inner margin; submarginal band as a faint stripe; marginal band following the outer margin contour; underside with the same dorsal pattern. Hindwing with the same forewing pattern, except being lighter proximally and without the submarginal stripe. Abdomen. Dorsally brown; ventrally light brown with two lateral dark brown stripes. Genitalia (Figs. 3A3D): Tegumen triangular in dorsal view, with the anterior margin round. Uncus absent. Valva entitre, sub-elliptical; sacculus developed, consisting of an anterior projection with rounded apex. Labides absent. Fultura inferior or juxta sclerotized, shaped like an inverted U. Saccus with a short anterior projection. Subscaphium smooth. Aedeagus rectilinear with a spine near the vesica; ejaculatory bulb rounded, foramen lateral; vesica bilobed, lobes with dense sclerotized spiniform cornuti.

Description () Head: Same as in the male except for the antenna less pectinated. Thorax: Same as in the male. Abdomen: Same as in the male. Genitalia (Fig. 3E): Seventh sternite smooth; ostium membranous not fused with the seventh sternite; antrum short and membranous, except for a sclerotized bracket-shaped support close to corpus bursae; ductus bursae short and membranous; corpus bursae extending beyond the seventh sternite; signa consisting of several microspicles and a falciform spine. Bulla seminallis arising from a ventral pouch on the posterior portion of corpus bursae. Lamella antevaginalis and postvaginalis absent.

Etymology. The specific epithet, oya is the Brazilian name for the female orisha who commands the winds, lightning and storms. In the native culture of the Yoruba people, orishas represent spirits sent for the guidance of all creation and of humanity.

The Portuguese spelling comes from the Yoruba ya which means she tore. She is the patron of the Niger River, known to the Yoruba as the Odo-ya. The specific epithet is a tribute to women and to Brazilian black culture. A noun in apposition.

Distribution. The few records for this species are from medium and low altitudes (800 m to 1,200 m a.s.l.) in the Serra do Mar and Serra da Mantiqueira mountain chains, in a narrow region of the Atlantic Forest near the border between the states of So Paulo and Rio de Janeiro.

Remarks: Some adults were obtained from immature stages hand-collected on Piper reitzii plants at the Parque Nacional do Itatiaia, in the state of Rio de Janeiro and reared to adults in laboratory (see Methods section).

Type series. HOLOTYPE , ex larva: BRAZIL: Rio de Janeiro: Itatiaia:, Parque Nacional do Itatiaia 22 27 01.5 S 44 37 14.0 W, 1,174 m asl, 03-VIII-2016, Simeo M., Tamara A. & Mariana S leg. Deposited in the Zoological Collection of the Museu da Biodiversidade da Universidade Estadual de Campinas (ZUEC), Campinas, So Paulo, Brazil.

PARATYPES (all from Brazil): Rio de Janeiro: Itatiaia, 1 and 2 , ex larva, Parque Nacional do Itatiaia, 22 27 01.5 S 44 37 14.0 W, 1,174 m asl, 03-VIII-2016, Simeo M., Tamara A. & Mariana S. leg. (ZUEC). So Paulo: Salespolis, 1 and 1, Estao Biolgica de Boraceia, 23 39S 45 54W, 850 m asl, 28-X/ 01-XI-2016, Simeo M., Tamara A. & Andr T leg. (MZUSP).

Eois ewa Moraes & Stanton sp.nov. (Figs. 2C2D, 4)

Figure 4. Male and female genitalia of Eois ewa sp.nov. paratype.

A. Male genitalia, genital capsule, dorsal view. B. Male genitalia, genital capsule, ventral view C. Male genitalia, genital capsule, lateral view. D. Male genitalia, aedeagus, lateral view. E. Female genitalia, lateral view. Line drawings by Simeo Moraes.

Diagnosis ( and ). Forewing dorsal view with dark brown maculae on the outer margin. Forewings and hindwings with two vertical mirrored bands on discal cell closure, continuous with dorsally dark brown abdominal segments A5 and A6 (Fig. 2C).

Description () (Figs. 2C2D). Head: Brown. Frons brown, vertex brown. Labial palp light brown. Thorax: Predominantly light brown. Prothoracic collar with iridescent gold scales. Tegulae light brown. Forewing background rusty brown; two sinuous black stripes on the wing base, from de trunk of R vein, reaching the inner margin; two vertical mirrored bands on discal cell closure, from the trunk of R4+R5 to inner margin; dark brown maculae on the outer margin, merged with the discal bands in the region of discal cell closure; underside with the same dorsal pattern. Hindwing with the same forewing pattern, except with the light brown background and the outer maculae replaced by three bands composed of brown spots. Abdomen: Dorsally brown; dark brown central macula on abdominal tergites A1-A4, abdominal tergites A5-A6 dark brown; ventrally light brown with patches of dark brown scales on the sternite A2-A8 margin. Genitalia (Figs. 4A4D): Tegumen triangular in dorsal view, with the anterior margin round. Uncus absent. Valva trapezoidal; sacculus developed, consisting of an anterior projection with rounded apex. Labides absent. Transtila sclerotized, squared. Fultura inferior or juxta sclerotized, shaped like a U. Saccus with a short anterior projection. Aedeagus rectilinear and smooth; ejaculatory bulb rounded, foramen lateral; vesica bilobed, lobes with two patches of sclerotized spiniform cornuti.

Description (). Head: Same as in the male except for the antenna less pectinated. Thorax: Same as in the male. Abdomen: Same as in the male. Genitalia (Fig. 4E): Seventh sternite smooth; ostium membranous not fused with the seventh sternite; antrum short and membranous, except for a sclerotized ring close to corpus bursae; ductus bursae short and membranous; corpus bursae with multiseriated signa, signa consisting of several microspicles displaced at the anterior portion of corpus bursae. Accessory bag smooth. Lamella antevaginalis and postvaginalis absent.

Etymology. The specific epithet, ewa comes from Yoruba Yew. In Brazil, ewa is name for the female orisha and river deity from the Yew river, located in the ancient Egbado tribe (present-day city of Yewa). In the native culture of the Yoruba people, orishas represent spirits sent for the guidance of all creation and of humanity.

Ewa represents the gift of divination and intuition. She also represents the mutations, transformations and the perception of what is beautiful and what is ugly. The specific epithet is a tribute to women and to Brazilian black culture. A noun in apposition.

Distribution. The four individuals known were obtained from reared larvae collected on the host plant Peperomia hispidula in humid montane forests (altitude of 1,100 m a.s.l.) at the Itatiaia National Park, in the state of Rio de Janeiro.

Type series. HOLOTYPE , ex larva: Rio de Janeiro: Itatiaia: Parque Nacional do Itatiaia, 22 25 37.8 S 44 37 07.0 W, 1,100 m asl, 30-VI-2017, Lydia Y., Mariana S. & Simeo M. leg. Deposited in the Zoological collection of the Museu da Biodiversidade da Universidade Estadual de Campinas (ZUEC), Campinas, So Paulo, Brazil.

PARATYPES (all from Rio de Janeiro, Brazil): Itatiaia: 2 and 4, ex larva, Parque Nacional do Itatiaia, 22 25 37.8 S 44 37 07.0 W, 1,100 m asl, 30-VI-2017, Lydia Y., Mariana S. & Simeo M. leg. (ZUEC); 1, ex larva: 30-VI-2017, Lydia Y., Mariana S. & Simeo M. leg. (MZUSP).

Eois oxum Moraes & Freitas sp.nov. (Figs. 2E2F, 5)

Figure 5. Female genitalia of Eois oxum sp.nov. holotype.

A. Genitalia, dorsal view. B. Genitalia, ventral view C. Genitalia, lateral view. Line drawings by Simeo Moraes

Diagnosis (). Forewing costal margin brown, olive green at the wing base and apex, in dorsal view. Hindwing upperside olive green at the wing base. Forewing and hindwing with a black dot on the center of discal cell. Abdominal segments A1 and A2 olive green dorsally (Fig. 2E).

Description () (Figs. 2E2F). Head: Brown. Frons brown, vertex brown. Labial palp light brown. Thorax: Predominantly olive green. Prothorax brown and prothoracic collar olive green. Tegulae olive green. Forewing background olive green, costal margin brown; a black dot in the center of discal cell; two vertical mirrored dark brown stripes in the discal cell closure, from costal margin to inner margin; two post discal bands, faint from costal margin to R₅, dark brown from R₅ to inner margin; dark brown maculae on the tornus region, merged with the post discal bands on the region close to tornus; outer margin delineated by rusty brown scales followed by a fringe of yellow scales; underside with the same dorsal pattern but with light brown background and rusty brown bands. Hindwing with the same forewing pattern, except for the darker apex and the delineated post discal bands. Abdomen: Dorsally olive green on segments A1-A2, beige on segments A3-A7, ventrally beige. Genitalia (Fig. 5): Seventh sternite smooth; ostium sclerotized not fused with the seventh sternite; antrum short and membranous, except for a sclerotized ring close to corpus bursae; ductus bursae short and membranous; corpus bursae extending beyond the seventh sternite, signa consisting of several microspicles and a falciform spine. Bulla seminallis arising from a ventral pouch on the posterior portion of corpus bursae Lamella antevaginalis absent. Lamella postvaginalis sclerotized, square shaped.

Etymology. The specific epithet oxum comes from Yoruba Osun. It is the Brazilian name of the female orisha and river deity who reigns over fresh waters. In the native culture of the Yoruba people, orishas represent spirits sent for the guidance of all creation and of humanity.

Oxum is considered the lady of beauty, fertility, money and sensitivity. Its name derives from the Osun River, which flows in Yorubaland, the Nigerian region of js. The specific epithet is a tribute to women and to Brazilian black culture. A noun in apposition.

Distribution. The single record came from a site of montane rainforest in a region with elevations ranging from 800 m to 1,000 m a.s.l. in the Serra do Mar mountain chain, in So Paulo State.

Remarks: Eois oxum is represented by a singleton collected on a lightrap. Despite having returned to the sampling site several times no additional individuals were collected. Regardless of having just one specimen available, the idiosyncratic wing pattern and the morphology of genilalia justifies the description of this new taxon based only on the holotype.

Type series. HOLOTYPE : BRAZIL: So Paulo: Salespolis, Estao Biolgica de Boraceia, 23 39 S 45 54 W, 850 m asl, 28-X/ 01-XI-2016, Simeo M., Tamara A. & Andr T leg. Deposited in the Zoology Collection of the Museu da Biodiversidade da Universidade Estadual de Campinas (ZUEC), Campinas, So Paulo, Brazil.

Discussion

Although the diversity of Eois has been highlighted in previous studies based on molecular evidence (Strutzenberger et al., 2011; Wilson et al., 2012; Moraes et al., 2021), the lack of researchers working on this diversity and providing stability for the names through formal description of new taxa precluded a comprehensive taxonomic treatment so that the proper description of this huge diversity remains a taxonomic challenge.

In the present study, we provided a preliminary taxonomic assessment for a small clade of Eois; a broader taxonomic sampling and additional evidence (molecular and morphological) will be needed to deal with larges clades, such as those of E. olivacea and E. tegularia. In short, although the present study is a small contribution for a clade that is clearly composed of a large number of species, including several complexes of cryptic species, we hope that it contributes to a better understanding of the genus Eois. Moreover, we believe that forthcoming studies in this group can take advantage of several sources of evidence, including morphology, molecular data and host plant use among other not yet properly explored (e.g., data from immature stages). In this context of integrative taxonomy, the distinct evolutionary lineages (i.e., distinct species) can be better recognized and defined, unveiling the real biodiversity of this large genus of moths.

Funding Statement

This work was supported by the Fundao de Amparo Pesquisa do Estado de So Paulo (FAPESP) with the scholarship awarded by SSM (grants FAPESP 2015/170475, FAPESP 2016/201965), YZM (2019/02727-1) and MAS (FAPESP 2015/26823-9). AVLF thanks the Brazilian Research CouncilCNPq (grant 303834/2015-3), the FAPESP (grants no. 2011/50225-3, 2012/50260-6, 2013/50297-0) and The United States Agency for International DevelopmentUSAID/the U.S. National Academy of Sciences (NAS), under the PEER program (Sponsor Grant Award Number: AID-OAA-A-11-00012). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.