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A informação e a educação antidopagem (EAD) são direitos dos atletas e a proximidade destes com as confederações desportivas brasileiras (CB) pode potencializar o combate ao doping. Objetivos: analisar as informações sobre EAD promovidas pelas CB em seus websites e mídias sociais (WMS) e verificar se há relação entre estes dados, a quantidade de pessoal sancionado e a possibilidade de medalhas nos últimos Jogos Olímpicos e Paralímpicos de verão e inverno (JOP) (Tokyo, 2020 e Beijing, 2022). Foram realizadas buscas nos WMS das CB sobre antidopagem nos últimos 180 dias; nos websites da WADA, da Autoridade Brasileira de Controle de Dopagem e das Federações Internacionais para quantificar os atletas e pessoal de apoio sancionado; além do levantamento dos resultados dos últimos JOP. Resultados: as CB realizam poucas ações de EAD em seus WMS, das 41 entidades analisadas, 34 (82.9%) não possuíam o Código Brasileiro Antidopagem para acesso em seus sítios eletrônicos; e 21 (51.2%) não realizaram nenhuma postagem sobre o assunto durante os seis meses de monitoramento. Não ficou evidenciada a correlação entre a EAD disponibilizada e a quantidade de pessoal sancionado, ou a possibilidade de medalha. No Brasil, a EAD necessita realizar avanços, devendo as CB realizar mais ações nesta área para os atletas. Palavras-chave: Dopagem; Ambiente Virtual; Atleta; Esporte

Objectives To characterize a novel acquired MBL, BIM-1, in a Pseudomonas #2 (subgroup P. guariconensis) strain isolated from the Aurá river located in the Brazilian Amazon hydrographic basin. Methods WGS using an Illumina® MiSeq System was used to characterize the genome of Pseudomonas sp. IEC33019 strain. Southern blotting/hybridization assays were performed to confirm the location of the MBL-encoding gene, blaBIM-1 (Belém Imipenemase). Antimicrobial susceptibility testing, cloning, and biochemical and phenotypic characterization were performed to determine BIM-1 kinetics. Results The IEC33019 strain showed high resistance rates to β-lactams, ciprofloxacin and aminoglycosides, being susceptible only to polymyxins and susceptible, increased exposure to aztreonam. WGS analysis revealed a novel acquired MBL-encoding gene, blaBIM-1, found as a gene cassette inserted into a class 1 integron (In1326) that also carried qnrVC1 and aadA11e. In1326 was located in a complex transposon, Tn7122, carried by a 52.7 kb conjugative plasmid (pIEC33019) with a toxin/antitoxin system (vapB/vapC). BIM-1 belongs to the molecular subgroup B1 and shares 70.2% and 64.9% similarity with SIM-1 and IMP-1, respectively. Kinetics analysis of BIM-1 showed hydrolytic activity against all β-lactams tested. Conclusions BIM-1 is a novel acquired MBL encoded by a gene carried by mobile genetic elements, which can be transferred to other Gram-negative bacilli (GNB). Because the IEC33019 strain was recovered from a river impacted by a populous metropolitan region with poor basic sanitation and served by limited potable freshwater, it would be important to establish the role of the BIM-1-producing GNB as nosocomial pathogens and/or as colonizers of the riverside population in this geographical region.

In this work, a kinematic wave-packet model is used to predict installed-jet noise. Large-eddy simulation results of freejets, for Mach numbers 0.4 and 0.9, are used to obtain parameters of wave packets representing large-scale turbulent structures, which were used to provide a model source for the Lighthill analogy used to predict far-field noise spectra. The source amplitude in the model is calibrated using noise measurements for a freejet, and such a wave-packet source is used to predict noise of the same jet in an installed configuration using a tailored Green’s function. Results from the prediction model are compared to installed-jet experimental data for four different observer positions and a large range of frequencies. Overall, the model predicts both directivities and amplitudes similar to the experimental data, with a hump in the generated noise for lower Strouhal numbers and a clear peak near a Strouhal number of 0.2. This low-order model is fast and flexible, and it is expected to be helpful in preliminary aircraft design.

Dysfunction of the adipose tissue metabolism is considered as a significant hallmark of aging. It has been proposed that α-β hydrolase domain containing 5 (ABHD5) plays a critical role in the control of lipolysis. However, the role of ABHD5 in the control of lipolysis during aging or exercise is unknown. Here we combined the experimental mouse model with transcriptomic analyzes by using murine and human databases to explore the role of ABHD5 in the adipose tissue during aging and in response to exercise. Transcriptomic data revealed a downregulation of Abhd5 messenger RNA levels in the subcutaneous white adipose tissue (scWAT) over time in individuals from 20 to 69 years old. Aged mice displayed dramatic reduction of ABHD5 protein content and lipolytic-related proteins in the scWAT. Interestingly, 4 weeks of high-intensity interval training increased ABHD5 protein level and restored the lipolytic pathway in the scWAT of aged mice. Altogether, our findings demonstrated that aging affects ABHD5 content in the adipose tissue of mice and humans. Conversely, exercise increases ABHD5 activity, recovering the lipolytic activity in aged mice.

Caffeine is one of the most widely used substances as recreational drug for performance-enhancement in sport, underpinned by a strong evidence base. Although the effects of caffeine are widely investigated within the scope of performance physiology, the molecular effects of caffeine within skeletal muscle remain unclear. Evidence from in vitro and in vivo models suggest that caffeine regulates the glucose metabolism in the skeletal muscle. Moreover, caffeine seems to stimulate CaMKII, PPARδ/β, AMPK and PGC1α, classical markers of exercise-adaptations, including mitochondrial biogenesis and mitochondrial content. This review summarizes evidence to suggest caffeine-effects within skeletal muscle fibers, focusing on the putative role of caffeine on mitochondrial biogenesis to explore whether caffeine supplementation might be a strategy to enhance mitochondrial biogenesis.

The Global South has witnessed increasing sampling of its immense biological diversity during the past century. However, the diversity of many regions remains unknown, even at pristine and highly threatened places, such as in the Atlantic Forest; and for bioindicator, umbrella, and flagship groups. The present study reports the first butterfly list of the Parque Estadual Intervales, São Paulo, Brazil and surroundings, a key protected area in the last massive continuous of the Atlantic Forest. We compiled data from museums and four years of field work, under three sampling methods. We also aimed at providing resources to support conservation efforts by analyzing 27 years of climatic data (detailed in the Supplementary Material, in English and in Portuguese), discussing our results also for non-academics, and producing scientific outreach and educational material. A companion article dealt with the experiences of science outreach and capacity development, and illustrated the butterfly catalogue of the species sampled in the park. We found 312 species that sum to 2,139 records. The museum had 229 species (432 records), and we sampled 142 species (1,682 individuals), in a total effort of 36,679 sampling hours (36,432 trap and 247 net and observation hours). The richest families were Nymphalidae (148 species) and Hesperiidae (100 species). Most species were sampled exclusively by active methods (79.8%), but other sources (passive sampling, citizen science, etc.) also found unique records. We found the highest diversity metrics from January to May, and we demonstrated that winter months had less richness and abundance. We illustrated the 20 species common to all regions, and listed those that were found more than seven months in the year, as well as the most abundant species in trap sampling, with forest dwellers as well as species common to open and fragmented areas. The dominant species in our trap datasets was the iridescent white morpho, Morpho epistrophus (Fabricius, 1796), and we suggest it to become the park butterfly mascot. Resumo O Sul Global testemunhou crescente amostragem de sua imensa diversidade biológica durante o século passado. Entretanto, a diversidade de muitas regiões permanece desconhecida, mesmo em locais pristinos e altamente ameaçados, como na Mata Atlântica; e para grupos bioindicadores, guarda-chuva e emblemáticos. O presente estudo reporta a primeira lista de borboletas do Parque Estadual Intervales, São Paulo, Brasil e arredores, uma unidade de conservação chave no último maciço contínuo de Mata Atlântica. Compilamos dados de museus e quatro anos de campo, sob três métodos de amostragem. Também visamos oferecer recursos para apoiar os esforços de conservação, analisando 27 anos de dados climáticos (detalhados no Material Suplementar, em inglês e em português), discutindo nossos resultados numa linguagem também para não acadêmicos, e produzindo material de divulgação científica e educativos. Um artigo irmão tratou das experiências de divulgação científica e capacitação, e ilustrou o catálogo de borboletas das espécies amostradas no parque. Encontramos 312 espécies em 2.139 registros. O museu tinha 229 espécies (432 registros), e amostramos 142 espécies (1.682 indivíduos), em um esforço total de 36.679 horas de amostragem (36.432 armadilhas e 247 horas de rede e observação). As famílias mais ricas foram Nymphalidae (148 espécies) e Hesperiidae (100 espécies). A maioria das espécies foi amostrada exclusivamente por métodos ativos (79,8%), mas outras fontes (passiva, ciência cidadã, etc.) também encontraram registros únicos. Encontramos as maiores métricas de diversidade de janeiro a maio, e demonstramos que os meses de inverno tiveram menos riqueza e abundância. Ilustramos as 20 espécies comuns a todas as regiões, e listamos aquelas que foram encontradas em mais de sete meses no ano, bem como as espécies mais abundantes em armadilhas, com espécies florestais e também comuns em áreas abertas e fragmentadas. A espécie dominante em nossas armadilhas foi a morfo branca iridescente, Morpho epistrophus (Fabricius, 1796), e sugerimos que se torne a borboleta mascote do parque.

The widest spanwise scales in turbulent channel flows are studied through the use of three periodic channel-flow simulations at friction Reynolds number $\mathrm{Re}_{\tau}=550$. The length and height of the channels are the same in all cases ($L_x/h=8\pi$ and $L_y/h=2$ respectively), while the width is progressively doubled: $L_z/h = \{4\pi, 8\pi, 16\pi\}$. The effects of increasing the domain can not be determined with statistical significance in our simulations, since the difference in the statistics between the simulations is of the same order as the errors of convergence. A channel flow similar to the smaller one ($\textit{J. Fluid Mech.}$, vol. 500, 2004, pp. 135--144), which was averaged over a very long time, was used as a reference. The one-dimensional spanwise spectrum of the streamwise velocity is computed with the aim of assessing the domain-size effect on the widest scales. Our results indicate that $90\%$ of the total streamwise energetic fluctuations is recovered without a significant influence of the size of the domain. The remaining $10\%$ of the energy reflects that the widest scales in the outer layer are the ones most significantly affected by the spanwise length of the domain. The power-spectral density for $k_z = 0$ remains constant even if the size of the domain in the spanwise direction is increased up to 4 times the standard spanwise length, indicating that wide, spanwise coherent structures are not an artifact of domain truncation.

Plane Couette flow at Re=1200 (based on the channel half-height and half the velocity difference between the top and bottom plates) is investigated in the minimal multi-scale flow unit (i.e. a flow unit with only two spanwise integral length scales), a system for which the computation of invariant solutions that are physically representative of the turbulent state has been understood to be challenging. To address this challenge, our approach is to employ an accurate reduced-order model with 600 degrees of freedom (Cavalieri & Nogueira, Phys. Rev. Fluids, vol. 7, 2022, L102601). Using the two-scale energy budget and the temporal cross-correlation of key observables, it is first demonstrated that the model contains most of the multi-scale physical processes identified recently (Doohan et al., J. Fluid Mech., vol. 913, 2021, A8): i.e. the large- and small-scale self-sustaining processes, the energy cascade for turbulent dissipation, and an energy-cascade mediated small-scale production mechanism. Invariant solutions of the reduced-order model are subsequently computed, including 96 equilibria and 43 periodic orbits. It is found that all the computed equilibrium solutions are not able to reproduce sound energy balance associated with the multi-scale dynamics of turbulent state. Incorporation of unsteadiness into invariant solutions is seen to be essential for a sensible description of the multi-scale turbulent dynamics and the related energetics, at least in this type of flow, as periodic orbits with a sufficiently long period are mainly able to describe the complex spatiotemporal dynamics associated with the known multi-scale phenomena.

Drop-on-demand printing using colloidal or pigmented inks is prone to the clogging of printing nozzles, which can lead to positional deviations and inconsistently printed patterns (e.g., data matrix codes, DMCs). However, if such deviations are detected early, they can be useful for determining the state of the print head and planning maintenance operations prior to reaching a printing state where the printed DMCs are unreadable. To realize this predictive maintenance approach, it is necessary to accurately quantify the positional deviation of individually printed dots from the actual target position. Here, we present a comparison of different methods based on affinity transformations and clustering algorithms for calculating the target position from the printed positions and, subsequently, the deviation of both for complete DMCs. Hence, our method focuses on the evaluation of the print quality, not on the decoding of DMCs. We compare our results to a state-of-the-art decoding algorithm, adopted to return the target grid positions, and find that we can determine the occurring deviations with significantly higher accuracy, especially when the printed DMCs are of low quality. The results enable the development of decision systems for predictive maintenance and subsequently the optimization of printing systems.

A brief historical review regarding the type locality of Euptychia stigmatica Godman, 1905 was conducted, which suggests that its type locality is actually Rio de Janeiro, Brazil, rather than northeastern Argentina, as previously purported. Consequently, E. stigmatica and its senior synonym E. cyanites Butler, 1871, are regarded to be two species-group names representing a taxon in the euptychiine genus Caeruleuptychia Forster, 1964 known from the Brazilian Atlantic Forest. A lectotype is designated for E. cyanites. Additionally, two closely related species are named and described using an integrative approach with morphological and molecular evidence. Caeruleuptychia harrisi Nakahara & Freitas, sp. nov. and C. aemulatio Nakahara & Willmott, sp. nov. both occur in Amazonia and COI barcode data recovered these taxa as part of the caerulea clade of Caeruleuptychia.

Este resumo aborda uma breve pesquisa feita sobre os efeitos do turismo ao meio ambiente no Brasil. O turismo é uma importante indústria em todo o mundo, contribuindo significativamente para o crescimento econômico e a criação de empregos em muitos países. No entanto, essa indústria também pode ter efeitos negativos sobre o meio ambiente e a qualidade de vida das comunidades locais, especialmente quando se trata de poluição. No Brasil, o turismo tem sido responsável por um aumento significativo na poluição de muitas áreas, incluindo praias, rios, florestas e cidades. A poluição causada por essa prática pode assumir várias formas, como a produção de lixo, a emissão de gases poluentes, o uso excessivo de água e a degradação da paisagem.

Fullerene-based polymers and oligomers combined with non-fullerene acceptors show extremely high efficiencies in organic photovoltaic devices. Furthermore, fullerene-based materials are of interest for use in anti-cancer and anti-viral treatments, where their presence can enhance the efficacy of medication considerably. Therefore, it remains important to understand their morphology and electronic properties to improve devices and technological applications. The main goal of this study is to prepare and characterize Langmuir and Langmuir-Schaefer films of PCBM-based materials to investigate the influence of different solvents such as chloroform, toluene, and xylene, and co-components on their morphology. PCBM-based materials were thus studied either alone or in mixtures with a polythiophene derivative (poly(3-hexythiophene), P3HT) commonly used in organic photovoltaic devices. The formation of Langmuir films was studied using surface pressure isotherms and Brewster's angle microscopy (BAM), where the homogeneity, phase behavior, and morphology of the films were investigated. In addition, Langmuir-Schaefer films were characterized by UV-visible absorption spectroscopy, atomic force microscopy (AFM), and Raman spectroscopy, providing information on the morphology of the solid films. This study has shown that it is possible to successfully fabricate Langmuir and Langmuir-Schaefer films of PCBM and PCBM-based oligomers and polymers, both pure and in mixtures with P3HT, to compare their organization, roughness, and optical properties. With the Langmuir films, it was possible to estimate the area of the molecules and visualize their aggregation through BAM images, establishing a relationship between the area occupied by these materials and the solvent used. All characterization techniques corroborate that the use of chloroform significantly reduced the roughness of the LS films mixed with P3HT and also presented a higher ordering compared to films prepared with xylene solutions.

Forsterinaria Gray, 1973 = Haywardina Forster, 1964, preocc. (not Aczél, 1952 (Diptera)) = Forsterina Lamas, 1977, missp. = Forsterinonia Brown, 1992, missp. = Guaianaza Freitas & Peña, 2006 anophthalma (C. Felder & R. Felder, 1867) antje Peña & Lamas, 2005 [Peña & Lamas (2005, Revista peruana de Biología, 12(1): 5-48)] boliviana (Godman, 1905) = vetula (Forster, 1964), nom. nud. chaniorum Viloria & Costa, 2019 [Costa et al. (2019, Anartia, 29: 20-48)] coipa Peña & Lamas, 2005 [Peña & Lamas (2005, Revista peruana de Biología, 12(1): 5-48)] difficilis (Forster, 1964) = anachoreta Pulido & Andrade, 2008 [Zubek & Pyrcz (2011, Genus, 22(2): 217-225)] emo Zubek, Pyrcz & Boyer, 2014 [Zubek et al. (2014, Neotropical Entomology, 43(1): 68-77)] enjuerma Peña & Lamas, 2005 [Peña & Lamas (2005, Revista peruana de Biología, 12(1): 5-48)] falcata Peña & Lamas, 2005 [Peña & Lamas (2005, Revista peruana de Biología, 12(1): 5-48)] guaniloi Peña & Lamas, 2005 [Peña & Lamas (2005, Revista peruana de Biología, 12(1): 5-48)] hannieri Zubek & Pyrcz, 2011 [Zubek & Pyrcz (2011, Genus, 22(3): 523-530)] inornata (C. Felder & R. Felder, 1867) = eusebia (Butler, 1877) - magdalena (Hayward, 1957) [Zubek & Pyrcz (2015, Zootaxa, 4028(4): 579-582)] itatiaia Peña & Lamas, 2005 [Peña & Lamas (2005, Revista peruana de Biología, 12(1): 5-48)] = otomara (J. Zikán & W. Zikán, 1968), nom. nud. [Lamas, unpublished data] necys (Godart, [1824]) = vastata (Butler, 1867) = pseudonecys (Strand, 1916) [Peña & Lamas (2005, Revista peruana de Biología, 12(1): 5-48)] = stellifera (J. Zikán & W, Zikán, 1968), nom. nud. [Lamas, unpublished data] neonympha (C. Felder & R. Felder, 1867) = polyphemus (Butler, 1867) = umbracea (Butler & Druce, 1872) = cyclops (Butler, 1877) pallida Peña & Lamas, 2005 [Peña & Lamas (2005, Revista peruana de Biología, 12(1): 5-48)] - aurita Peña & Lamas, 2005 [Peña & Lamas (2005, Revista peruana de Biología, 12(1): 5-48)] pichita Peña & Lamas, 2005 [Peña & Lamas (2005, Revista peruana de Biología, 12(1): 5-48)] pilosa Peña & Lamas, 2005 [Peña & Lamas (2005, Revista peruana de Biología, 12(1): 5-48)] pronophila (Butler, 1867) [Matos-Maraví et al. (2012, Molecular Phylogenetics and Evolution, 66: 54-68)] = pronophila (Butler, 1867), nom. nud. [Matos-Maraví et al. (2012, Molecular Phylogenetics and Evolution, 66: 54-68)] proxima (Hayward, 1957) pseudinornata (Forster, 1964) punctata Peña & Lamas, 2005 [Peña & Lamas (2005, Revista peruana de Biología, 12(1): 5-48)] pyrczi Peña & Lamas, 2005 [Peña & Lamas (2005, Revista peruana de Biología, 12(1): 5-48)] quantius (Godart, [1824]) = stelligera (Butler, 1874) [Peña & Lamas (2005, Revista peruana de Biología, 12(1): 5-48)] = fabiana (Butler, 1877) [Peña & Lamas (2005, Revista peruana de Biología, 12(1): 5-48)] = morima (Schaus, 1902) = wordhilda (J. Zikán & W. Zikán, 1968), nom. nud. [Lamas, unpublished data] rotunda Peña & Lamas, 2005 [Peña & Lamas (2005, Revista peruana de Biología, 12(1): 5-48)] rustica (Butler, 1868) - villarresi (Dognin, 1887) = weyrauchi (Hayward, 1964) - glendita Peña & Lamas, 2005 [Peña & Lamas (2005, Revista peruana de Biología, 12(1): 5-48)] stella (Hayward, 1957) = howarthi (Hayward, 1962), Published as part of Espeland, Marianne, Nakahara, Shinichi, Zacca, Thamara, Barbosa, Eduardo P., Huertas, Blanca, Marín, Mario A., Lamas, Gerardo, Benmesbah, Mohamed, Brévignon, Christian, Casagrande, Mirna M., Fåhraeus, Christer, Grishin, Nick, Kawahara, Akito Y., Mielke, Olaf H. H., Miller, Jacqueline Y., Nakamura, Ichiro, Navas, Vanessa, Patrusky, Brooke, Pyrcz, Tomasz W., Richards, Lindsay, Tan, Denise, Tyler, Stephanie, Viloria, Angel, Warren, Andrew D., Xiao, Lei, Freitas, André V. L. & Willmott, Keith R., 2023, Combining target enrichment and Sanger sequencing data to clarify the systematics of the diverse Neotropical butterfly subtribe Euptychiina (Nymphalidae, Satyrinae), pp. 1-73 in Zoological Research 2023 on pages 60-61, DOI: 10.1111/syen.12590, http://zenodo.org/record/7909395

Orotaygetis Nakahara & Zacca, 2018 surui Nakahara, Zacca & Lamas, 2018 [Nakahara et al. (2018, Insecta Mundi, 0639: 1-38)], Published as part of Espeland, Marianne, Nakahara, Shinichi, Zacca, Thamara, Barbosa, Eduardo P., Huertas, Blanca, Marín, Mario A., Lamas, Gerardo, Benmesbah, Mohamed, Brévignon, Christian, Casagrande, Mirna M., Fåhraeus, Christer, Grishin, Nick, Kawahara, Akito Y., Mielke, Olaf H. H., Miller, Jacqueline Y., Nakamura, Ichiro, Navas, Vanessa, Patrusky, Brooke, Pyrcz, Tomasz W., Richards, Lindsay, Tan, Denise, Tyler, Stephanie, Viloria, Angel, Warren, Andrew D., Xiao, Lei, Freitas, André V. L. & Willmott, Keith R., 2023, Combining target enrichment and Sanger sequencing data to clarify the systematics of the diverse Neotropical butterfly subtribe Euptychiina (Nymphalidae, Satyrinae), pp. 1-73 in Zoological Research 2023 on page 61, DOI: 10.1111/syen.12590, http://zenodo.org/record/7909395

Modica Zacca, Casagrande & Willmott, genus novum. Type species — Euptychia confusa Staudinger, 1887, by present designation. Zoobank registration: https://zoobank.org/Nomenclatural Acts/D3CE81CE-5587-41D5-AFB6-934343C11D6F Systematic placement and diagnosis. Modica gen.n. is a member of the ‘ Splendeuptychia clade’ (Figure 10), in which its monophyly is strongly supported (FULL dataset SH-aLRT =100, UFB = 100). Its relationships to other members of the clade, however, are not clear; the genus is placed as sister to Parypthimoides, but support is inconclusive (FULL dataset SH-aLRT 100, UFB 43), and is further found within the same strongly supported clade that also contains Deltaya gen.n. (see under that genus), Scriptor, Emeryus, Colombeia and Malaveria (FULL dataset SH-aLRT 100, UFB 95). As with Deltaya gen.n., no morphological synapomorphies were identified for Modica gen.n., but these two genera share the same somewhat distinctive characters within Euptychiina (see under the former genus). Overall, the genus is best distinguished from phenotypically similar genera by the pale pupils of the HW ocellus in Cu 2 -Cu 1 being visible on the dorsal surface, by the VHW postdiscal ocelli in cells Cu 1 -M 3 and M 3 -M 2 being of similar size, round (not elongate) and each containing two enlarged, elongated silver pupils, and by the marginal line not widening in the VHW tornus (Figures 37 and 38). The genitalia of both sexes (Figure 39) are described below, and, as with Deltaya gen.n., they are broadly similar to those of a number of more or less distantly related euptychiine genera, in other words lacking obvious synapomorphies. The eighth abdominal segment of the female is only slightly pleated and expandable, similar to Scriptor and some related species but differing from others in which it is fully pleated and expandable, with this character varying within genera (e.g. within Paryphthimoides and Deltaya gen.n.). The female genitalia also lacks a sclerotized lamella antevaginalis and there is no sclerotized plate present on the ventral intersegmental membrane of the seventh and eighth abdominal segments, unlike Scriptor and some species of Deltaya gen.n. Characters that differ among the genera within the clade in which Modica gen.n. is placed are summarized in Table 1. Etymology. The generic name is a feminine Latin adjective treated as a noun in the nominative singular, meaning something that is modest, ordinary, average, in reference to the ‘typical’ euptychiine morphology of this genus and its lack of obvious distinguishing characters. Description (Figures 37 – 39). Some notable characters include: eyes setose; pterothoracic legs dorsally slightly darker, tibia with two principal longitudinal rows of spines ventrally, pair of spurs of similar length at distal end of tibia, first tarsomere with three principal longitudinal rows of spines ventrally, remaining tarsomeres with four principal longitudinal rows of spines ventrally. Medium-sized Euptychiina (FW length typically 21 – 28 mm), FW triangular and rather rounded at apex, HW rounded. No strong sexual dimorphism: Dorsal wings dark brown to greyish brown, pale pupils of ocellus in cell Cu 2 -Cu 1 visible on DHW, no androconial scales present. Ventral wings greyish brown to yellowish brown; relatively broad, dark brown to reddish brown discal and postdiscal lines traversing both wings; VFW with three postdiscal ocelli in cells Cu 1 -M 3, M 3 -M 2, M 2 -M 1, anterior ocellus more clearly marked than remainder, lying within a broad dark brown band (umbra), with this band and adjacent area basally in middle of wing tinged yellowish in M. myncea comb.n. and M. confusa comb.n.; VHW similar to VFW but with five postdiscal ocelli between Cu 2 and Rs, those in cells Cu 2 -Cu 1 and M 2 -M 1 typically slightly larger, black-centred with two silver dots in each ocellus as pupils, ocellus in M 1 -Rs similar but much smaller, and those in cell Cu 1 -M 2 with dark brown centres and elongate silver pupils; marginal line thin and even throughout, not thickening at tornus. Male 8th abdominal tergite reduced dorsally, leaving a sclerotized strip along anterior edge and usually an isolated sclerotized patch in posterior portion. Male genitalia with uncus longer than tegumen, brachia approximately parallel with uncus and about two-thirds its length; valvae elongate with dorsal edge straight or with slight projection; aedeagus adorned with scattered small spines in some species, and with or without cornuti. Female genitalia has 8th tergite reduced to a posterior sclerotized patch about two-thirds width of segment, intersegmental membrane between seventh and eighth abdominal segments only somewhat expandable with no strongly sclerotized plate ventrally, eighth segment with large irregular lateral sclerotized plate extending further dorsally at anterior edge, lamella antevaginalis and antrum unsclerotized, ductus bursae unsclerotized, corpus bursae small, oval and with two narrow sub-parallel signa. Distribution and natural history (Figure 40). Modica gen.n. contains five described species and several undescribed species (Zacca et al., unpublished data), which occur in rainforest from sea level to 1300 m, ranging from southern Mexico to western Ecuador and throughout the Amazon and Guianas to south-eastern Brazil. The genus reaches its peak diversity in the western Amazon, where both sexes may be common throughout the understory of both disturbed and undisturbed forest, with some species also occurring along forest edges and in overgrown, shady plantations. Males of some species perch from 1 to 3 m in the forest understory in the morning and late afternoon, sometimes on hilltops, and both sexes are attracted to rotting fruit (DeVries, 1987; Zacca et al., pers. obs.). Notes on the immature stages of M. myncea comb.n. and M. confusa comb.n. were provided by Singer et al. (1983), with hostplants (natural and in captivity) including Cyperaceae, Palmae, Poaceae and Marantaceae (see also Beccaloni et al., 2008; Singer & Ehrich, 1993). Discussion. The type species for this genus, Euptychia confusa, was described by Staudinger (1884) based on an unstated number of specimens from Chiriquí, Panama, and a lectotype at the MfN was designated by Singer et al. (1983). The female illustrated in Staudinger (1884: pl. 80) agrees with the description, although it was incorrectly labelled as ‘ Euptychia myncea ’. We chose to designate Euptychia confusa as the type species for this genus since DNA barcode data suggest the possibility of cryptic species within Modica myncea comb.n. that remain to be resolved. Although strongly supported by the molecular data, Modica gen.n. lacks any clear morphological synapomorphies and it is thus not surprising that a close relationship among all of its constituent species was unnoticed until recently; M. confusa comb.n., M. myncea comb.n. and M. maripa comb.n. were hitherto placed in Cissia (e.g. Forster, 1964 [under the name Argyreuptychia]; Singer et al., 1983; Lamas, 2004; Brévignon, 2005) and M. fugitiva comb.n. and M. kamel comb.n. were placed in Magneuptychia (Benmesbah et al., 2018; Forster, 1964; Lamas, 2004). As discussed by Zacca, Casagrande, et al. (2018), most species placed in Cissia prior to that paper were presumably considered to be related because of their possession of a yellowish patch on the VFW, but that character is clearly homoplasious, and the Cissia of Lamas (2004) are now placed in six genera in two clades: Cissia, Vanima, Megisto, Modica, Paryphthimoides, and Vareuptychia. Benmesbah et al. (2018) noted that M. myncea comb.n., M. maripa comb.n., M. fugitiva and M. kamel comb.n. were likely closely related, based on morphology and preliminary molecular data, and suggested that a new genus might be needed to accommodate these species. Our phylogenetic analysis failed to strongly resolve the relationships of Modica gen.n. to other clades. These species therefore cannot reasonably be accommodated in any described genus without combining at least five described genera, along with Modica gen.n. and Deltaya gen.n., into a single, large genus of morphologically and ecologically dissimilar species, which would not correspond to any author ’ s prior taxonomic hypothesis. Modica Zacca, Casagrande & Willmott, gen.n. confusa (Staudinger, 1887), comb.n., was Cissia fugitiva (Lamas [1997]), repl. name, comb.n., was Magneuptychia = helle (Cramer, 1779), preocc. (not [Denis & Schiffermüller], 1775), comb.n., was Magneuptychia kamel (Benmesbah & Zacca, 2018), comb.n., was Magneuptychia [Benmesbah et al. (2018, Zootaxa, 4425(1): 115-145)] maripa (Brévignon, 2005), comb.n., was Cissia [Brévignon (2005, Lambillionea, 105(3)(1): 393-404)] myncea (Cramer, 1780), comb.n., was Cissia = myncena (Stoll, 1782), missp., comb.n., was Cissia = crantor (Fabricius, 1793), comb.n., was Cissia = clerica (Herrich-Schäffer, 1865), repl. name, comb.n., was Cissia = pytheus (MÖschler, 1883), comb.n., was Cissia = isolata (Kaye, 1921), comb. n., was Cissia [Kaye (1921, Memoirs of the Department of Agriculture of Trinidad and Tobago, 2: i-xii, 13-163, 1 pl.)], Published as part of Espeland, Marianne, Nakahara, Shinichi, Zacca, Thamara, Barbosa, Eduardo P., Huertas, Blanca, Marín, Mario A., Lamas, Gerardo, Benmesbah, Mohamed, Brévignon, Christian, Casagrande, Mirna M., Fåhraeus, Christer, Grishin, Nick, Kawahara, Akito Y., Mielke, Olaf H. H., Miller, Jacqueline Y., Nakamura, Ichiro, Navas, Vanessa, Patrusky, Brooke, Pyrcz, Tomasz W., Richards, Lindsay, Tan, Denise, Tyler, Stephanie, Viloria, Angel, Warren, Andrew D., Xiao, Lei, Freitas, André V. L. & Willmott, Keith R., 2023, Combining target enrichment and Sanger sequencing data to clarify the systematics of the diverse Neotropical butterfly subtribe Euptychiina (Nymphalidae, Satyrinae), pp. 1-73 in Zoological Research 2023 on pages 42-67, DOI: 10.1111/syen.12590, http://zenodo.org/record/7909395, {"references":["DeVries, P. J. (1987) The butterflies of Costa Rica and their natural history: papilionidae, Pieridae, Nymphalidae. Princeton: Princeton University Press, p. 288.","Singer, M. C., DeVries, P. J. & Ehrlich, P. R. (1983) The Cissia confusa species-group in Costa Rica and Trinidad (Lepidoptera: Satyrinae). Zoological Journal of the Linnean Society, 79, 101 - 119.","Beccaloni, G. W., Viloria, A. L., Hall, S. K. & Robinson, G. S. (2008) Catalogue of the hostplants of the Neotropical butterflies. Monografias Tercer Milenio. Sociedad Entomologica´Aragonesa (SEA) / Red Iberoamericana de Biogeografia y Entomologia Sistematica (RIBES) / Ciencia y Tecnologia para el Desarrollo (CYTED) / Natural History Museum, London, U. K. (NHM) / Instituto Venezolano de Investigaciones Cientificas, Venezuela (IVIC), Zaragoza, p. 536.","Singer, M. & Ehrich, P. (1993) Host specialization of satyrine butterflies, and their responses to habitat fragmentation in Trinidad. Journal of Research on the Lepidoptera, 30, 248 - 256.","Staudinger, O. (1884) I. Theil. Exotische Tagfalter in systematischer Reihenfolge mit Berucksichtigung neuer Arten. In: Staudinger, O. & Schatz, E. (Eds.) Exotische Schmetterlinge. Furth: G. Lowensohn, pp. 1 - 333.","Forster, W. (1964) Beitrage zur Kenntnis der Insektenfauna Boliviens XIX. Lepidoptera III. Satyridae. Veroffentlichungen der Zoologischen Staatssammlung Munchen, 8, 51 - 188.","Lamas, G. (2004) Atlas of Neotropical Lepidoptera. Checklist: Part 4 A Hesperioidea - Papilionoidea. Gainesville: Scientific Publishers / Association of Tropical Lepidoptera, p. 439.","Brevignon, C. (2005) Description de nouveaux Satyrinae provenant de Guyane franCaise (Lepidoptera, Nymphalidae). Lambillionea, 105, 393 - 404.","Benmesbah, M., Zacca, T., Casagrande, M. M., Mielke, O. H. H., Lamas, G. & Willmott, K. R. (2018) Taxonomic notes on Papilio ocypete Fabricius, 1776 and Papilio helle Cramer, 1779 with description of two new similar species from South America (Lepidoptera: Nymphalidae: Satyrinae). Zootaxa, 4425, 115 - 145."]}

Occulta Nakahara & Willmott, genus novum. Type species: Euptychia ocnus Butler, 1867, by present designation. Zoobank registration: https://zoobank.org/Nomenclatural Acts/7B2BBC71-C2FC-40B8-A24A-14A986151D85 Systematic placement and diagnosis. Occulta gen.n. is a member of the ‘ Splendeuptychia clade’, and it is rather distantly related to the remainder of the clade. Currently, Occulta gen.n. is modestly supported (SH-aLRT 100, UFB 75) as sister to a large clade including species-rich genera such as Caeruleuptychia, Paryphthimoides, and Splendeuptychia, among others (Figure 10). Based on hybrid enrichment data, Espeland et al. (2019a) recovered Occulta gen.n. (as ‘ Magneuptychia ocnus ’) as sister to ‘ Erichthodes ’ narapa (now Capronnieria narapa comb.n.) and Capronnieria galesus, although with only moderate support (BS and PP>0.75 Occulta gen.n. (Figure 30) resembles some species of Deltaya gen.n. (see Figures 33 and 34 below), but may be distinguished by possessing elongate, ‘smudge-like’ orangish spots with a silver marking in the middle in VHW cells M 2 and M 3, whereas the ocelli in these cells in Deltaya gen.n. are more rounded and have double silver spots encircled by a better defined yellowish ring. Furthermore, the dark ventral discal and postdiscal bands are typically narrower in Occulta gen.n. compared to Deltaya gen.n. species, perhaps with the exception of D. ocypete, whose ventral bands are often narrower in comparison with other closely related species. In particular, in Occulta gen.n. the VHW marginal band is of even width throughout, whereas this band forms a ‘wedge-shaped’ swelling at the tornus in Deltaya gen.n. In addition, Occulta gen.n. possesses a tiny, rather incomplete ocellus in VHW cell Cu 2, which is absent in Deltaya gen.n. The male genitalia also differ between Occulta gen.n. (Figure 31) and the type species of Deltaya gen.n. and close relatives (referred to as ‘core’ Deltaya gen.n.) (Figure 34), at least, by the lack of a developed ‘hump’ on the dorsal margin of the valva, and instead only have a slightly serrated region at the dorsal margin distal of the costa. In lateral view, the costa appears as a narrow plate in Occulta gen.n., whereas the costa appears as a somewhat trapezoidal plate in lateral view in ‘core’ Deltaya gen.n. See description of Deltaya gen.n. below for details about ‘core’ Deltaya gen.n. Etymology. The generic name is a Latin feminine adjective treated as a noun in the nominative singular, ‘occulta’, meaning a ‘hidden’ or ‘secret’ thing, in reference to the former concealment of this taxon within Magneuptychia. The generic name is also coined in alliteration with the species-group name. Description (Figures 30 and 31). Wing pattern and shape as illustrated (Figure 30). Other notable characters include eyes setose; pterothoracic legs dorsally darker, tibia with two principal longitudinal rows of spines ventrally, in addition to some spines laterally, pair of spurs of similar length at distal end of tibia, first tarsomere with three principal longitudinal rows of spines ventrally, remaining distal tarsomeres with four principal longitudinal rows of spines ventrally. Medium-sized Euptychiina (FW length typically 23 – 26 mm), DFW and DHW of males without obvious androconial scales, but long setiform scales visible in discal cell and adjacent areas, especially extending along inner margin. Male with 8th tergite a narrow stripe at basal side of the eighth abdominal segment, broad weakly sclerotized patch present at posterior side of eighth abdominal segment; genitalia as illustrated (Figure 31); costa appearing as a narrow plate in lateral view; cornuti present, otherwise genitalia as illustrated (Figure 31). Female genitalia (Figure 31) with intersegmental membrane of between seventh and eighth abdominal segment somewhat pleated and expandable with very weak sclerotization ventrally; lamella antevaginalis membranous; eighth segment with irregular lateral sclerotized plate narrowing slightly dorsally; pair of well-defined signa present. Occulta Nakahara & Willmott, gen.n. ocnus (Butler, 1867), comb.n., was Magneuptychia = gracilis (Weymer, 1911), comb.n., was Magneuptychia, Published as part of Espeland, Marianne, Nakahara, Shinichi, Zacca, Thamara, Barbosa, Eduardo P., Huertas, Blanca, Marín, Mario A., Lamas, Gerardo, Benmesbah, Mohamed, Brévignon, Christian, Casagrande, Mirna M., Fåhraeus, Christer, Grishin, Nick, Kawahara, Akito Y., Mielke, Olaf H. H., Miller, Jacqueline Y., Nakamura, Ichiro, Navas, Vanessa, Patrusky, Brooke, Pyrcz, Tomasz W., Richards, Lindsay, Tan, Denise, Tyler, Stephanie, Viloria, Angel, Warren, Andrew D., Xiao, Lei, Freitas, André V. L. & Willmott, Keith R., 2023, Combining target enrichment and Sanger sequencing data to clarify the systematics of the diverse Neotropical butterfly subtribe Euptychiina (Nymphalidae, Satyrinae), pp. 1-73 in Zoological Research 2023 on pages 35-67, DOI: 10.1111/syen.12590, http://zenodo.org/record/7909395, {"references":["Butler, A. G. (1867) Descriptions of some new species of Satyridae belonging to the genus Euptychia. Proceedings of the Zoological Society of London, 1867, 104 - 110.","Espeland, M., Breinholt, J., Barbosa, E. P., Casagrande, M., Huertas, B., Lamas, G. et al. (2019 a) Four hundred shades of brown: higher level phylogeny of the problematic Euptychiina (Lepidoptera, Nymphalidae, Satyrinae) based on hybrid enrichment data. Molecular Phylogenetics and Evolution, 131, 116 - 124.","Weymer, G. (1911) 4. Familie: Satyridae. In: Seitz, A. (Ed.) Die GrossSchmetterlinge der Erde. Stuttgart: A. Kernen, pp. 173 - 280."]}

Espeland, Marianne, Nakahara, Shinichi, Zacca, Thamara, Barbosa, Eduardo P., Huertas, Blanca, Marín, Mario A., Lamas, Gerardo, Benmesbah, Mohamed, Brévignon, Christian, Casagrande, Mirna M., Fåhraeus, Christer, Grishin, Nick, Kawahara, Akito Y., Mielke, Olaf H. H., Miller, Jacqueline Y., Nakamura, Ichiro, Navas, Vanessa, Patrusky, Brooke, Pyrcz, Tomasz W., Richards, Lindsay, Tan, Denise, Tyler, Stephanie, Viloria, Angel, Warren, Andrew D., Xiao, Lei, Freitas, André V. L., Willmott, Keith R. (2023): Combining target enrichment and Sanger sequencing data to clarify the systematics of the diverse Neotropical butterfly subtribe Euptychiina (Nymphalidae, Satyrinae). Zoological Research 2023: 1-73, DOI: 10.1111/syen.12590

Argentaria Huertas & Willmott, genus novum. Type species — Euptychia itonis Hewitson, 1862, by present designation. Zoobank registration: https://zoobank.org/Nomenclatural Acts/F5A5D4DD-82D3-40AA-BD88-978B9A55AB46 Systematic placement and diagnosis. Argentaria gen.n. is a member of the ‘ Amphidecta clade’, in which its monophyly is strongly supported in all datasets (FULL dataset, SH-aLRT 100, UFB 100, Figure 6). However, its relationships to other members of the clade, which include (among described species) Zischkaia, Amphidecta, ‘ Euptychia ’ ordinata / insignis, and ‘ Pharneuptychia ’ innocentia, are not strongly resolved. The new genus can be distinguished from other Euptychiina by the combination of the following three characters: (a) the VFW has a postdiscal series of ocelli extending from cell 2A-Cu 2 to M 2 -M 1, with these ocelli similar in form and elongate parallel to the wing margin, often with either a linear silvery pupil or double pupils in each cell (Figure 17). In some individuals of A. salvini comb.n., the ocelli are fused into a continuous band and the pupils absent, thus superficially resembling the dark postdiscal band, which surrounds the postdiscal ocelli in other species (e.g. Magneuptychia libye). (b) the VHW has the postdiscal ocellus in cell M 3 -M 2 elongated parallel to the veins, with the silvery pupil divided into two distinct spots, except in A. clementia comb.n., in which the two spots touch or are partly fused (Figure 17). A few other species have an elongated pupil similar to that in A. clementia comb.n., such as Splendeutychia purusana comb.rev. or Nhambikuara furina comb.n. (c) the VHW tornus in cell 2A-Cu 2 has several silver streaks, which appear to represent the pupils of ocelli in both the anterior and posterior half of the cell, with the former often being split into two or elongated and pinched in the middle, while the latter is visible as an additional silver spot in some species (e.g. A. itonis comb.n.) (Figures 18 and 19). Other genera with an elongate ocellus and silver pupil in cell 2A-Cu 2, such as Nhambikuara, have only a single pupil that is not as elongate as in Argentaria gen.n. The genitalia of both sexes (Figure 19) are described below and are broadly like those of a number of other relatively distantly related euptychiine genera (e.g. Amiga, Pseudeuptychia, Scriptor). Notable features include, in the male, the lack of cornuti in the aedeagus (similar to many other euptychiine genera), and in the female, the pleated, expandable intersegmental membrane between the seventh and eighth abdominal segments, antrum and lamella antevaginalis membranous, and small, round corpus bursae with slender, elongate, converging signa. The other two described genera within the ‘ Amphidecta clade’, namely Amphidecta and Zischkaia, each have distinctive male and female genitalia differing in numerous respects from Argentaria gen.n., with these distinctive characters apparently representing generic autapomorphies (Marín et al., 2017; Nakahara, Zacca, et al., 2019; Nakahara pers. obs.). Etymology. The generic name is a feminine Latin noun in the nominative singular, meaning a silver-mine, in reference to the distinctive silver scales arranged as spots on the ventral hindwing and forewing of species in this genus. Description (Figures 17 – 19). Some notable characters include: eyes naked; pterothoracic legs dorsally slightly darker, tibia with two principal longitudinal rows of spines ventrally, pair of spurs of similar length at distal end of tibia, first tarsomere with three principal longitudinal rows of spines ventrally, remaining tarsomeres with four principal longitudinal rows of spines ventrally. Small to medium-sized Euptychiina (FW length typically 15 – 25 mm), FW triangular and varying from being rather pointed (e.g. A. itonis comb.n.) to more rounded (e.g. A. quadrina comb.n.), HW rounded with margin variably undulating. No strong sexual dimorphism in most species: Dorsal wings dark grey brown, some species with white patches in discal part of DFW, and white patches in basal or discal part of DHW and yellowish or orangish distally, no androconial scales present except in male A. libitina comb.n., which has dark androconial scales lining the DFW cubital vein and basal part of vein Cu 2, and basal part of vein 2A. Ventral wings showing relatively large inter-specific variation in pattern across the genus, with ground colour ranging from dark grey-brown to paler yellowish brown; a dark discal and postdiscal line traversing both wings, ranging from a thin, irregular line to a straight, broad band, which may be absent or scarcely visible in some species; discal area of one or both wings often white to pale yellowish brown, sometimes extending basally or distally beyond postdiscal line; VFW with series of narrow postdiscal ocelli in cells 2A-Cu 2 to M 2 -M 1, elongated parallel to distal margin, usually with pupil present as single silver line or double silver spots, often fused into a broad band, variably surrounded by orange or yellow and in some species a further black border, ocelli variably distinct across species; VHW with a complex array of postdiscal ocelli in cells 2A-Cu 2 to M 1 -Rs, with that in Cu 2 -Cu 1 typically the largest, and, along with that in M 2 -M 1, often the only ocellus to be present as a black spot with a single, double, or further modified silver pupil, remaining ocelli typically lacking black with their silver pupils enlarged into spots or streaks, orange rings around ocelli expanded and fused in all species to form an orange background around the ocelli; silver pupil in cell M 3 -M 2 elongated and pinched in the middle (A. clementia comb.n.) or split into two spots (all other species), and that in cell 2A-Cu 2 similarly pinched or split, often forming three distinct spots in combination with a silver spot presumed to represent a posterior ocellus in that cell; two black submarginal lines parallel to wing margin with pale scaling between them, sometimes pierced by elongate silver pupils of the postdiscal ocelli. Male 8th abdominal tergite reduced dorsally, leaving a sclerotized strip along anterior edge and usually an isolated sclerotized patch in posterior portion, that can be broader (e.g. A. jadea comb.n.) or absent (e.g. A. pagyris comb.n.) in some species. Male genitalia with uncus longer than tegumen, brachia pointing dorsally of uncus or parallel with uncus and ranging from slightly longer than uncus (e.g. A. quadrina comb.n.) to very short/vestigial (e.g. A. kendalli comb.n., A. jadea comb.n., A. clorimena comb.n.); valva usually broadening at distal tip in lateral view, with distal tip sometimes with an inwardly pointing dorsal lobe (e.g. A. itonis, A. clementia, A. quadrina) and sometimes without (e.g. A. libitina comb.n., A. kendalli comb.n., A. clorimena comb.n.); vinculum in most species (but not all, e.g., A. pagyris) elongated above articulation with dorsal base of valva; aedeagus relatively straight and lacking cornuti. Female genitalia showing relatively little inter-specific variation, eighth tergite with small sclerotized posterior patch and thin strip at ventral anterior edge, intersegmental membrane between segments A7 and A8 pleated and expandable with a circular to quadrate sclerotized plate ventrally, eighth segment with large irregular oval lateral sclerotized plate, lamella antevaginalis and antrum unsclerotized, ductus bursae narrow and unsclerotized, corpus bursae small, circular and with two narrow, posteriorly converging signa. Distribution and natural history (Figure 20). Argentaria gen.n. species are found in rainforest and cloudforest from sea level to 2100 m, although the great majority of species are found below 1200 m. Similarly, although the genus occurs throughout the Neotropical region, only a couple of species occur west of the Andes, and the known centre of diversity is in the bamboo-rich forests of the south-western Amazon (Madre de Dios, Peru, and Acre, Brazil), where up to 10 species can be found in sympatry, and to a lesser extent in south-eastern Brazil (Atlantic region). All species occur in close association with bamboos (Poaceae: Bambusoideae: Bambuseae), including Guadua and various species of weeping bamboos (unpublished data), and many species are known from only a handful of widely scattered localities, with a number of species still undescribed. The immature stages were recently described for A. quadrina comb.n. by See et al. (2018), which was recorded feeding on the climbing bamboo Rhipidocladum racemiflorum with several other species having been reared in south-eastern Brazil (Freitas, 2022) and Ecuador (Willmott & Hall, unpublished data). Discussion. The type species for this genus, Euptychia itonis, was described by Hewitson (1862) from the ‘Amazon’ based on specimens in his collection and the collection of W. W. Saunders. The underside of a specimen was illustrated in his Figure 3 and it closely matches the three syntypes examined in the NHMUK, in particular in having a thin, broken dark brown postdiscal line in the white area of the VHW, which is unique within the genus to A. itonis comb.n. Butler (1867) placed all of the species included here in Argentaria gen.n. that were described at that time in his Division V, Subdivision 2, which he characterized as having the VHW ocelli represented as silver streaks with a large black tornal ocellus, with his correct recognition of the close relationships of the species in this group reflecting the distinctive VHW pattern of the genus. Weymer (1911) likewise successfully grouped described Argentaria gen.n. species in his ‘Clorimene [sic] group’, which he placed alongside his ‘Doxes group’, which corresponds to Nhambikuara. Forster ’ s (1964) decision to move Argentaria gen.n. species from Euptychia into his newly described genus Splendeuptychia, with type species Euptychia ashna, seems somewhat surprising, since Weymer (1911) evidently did not regard E. ashna as being closely related to the former two groups. Equally puzzling are Forster ’ s (1964) drawings of the male genitalia of A. clementia comb.n. and A. pagyris comb.n. (p. 129, figure 163, 164), which are rather different to specimens we have examined, most notably in showing an aedeagus with cornuti, which was not observed in any dissected Argentaria gen.n. In general, Forster (1964) separated numerous taxa from the genus Euptychia into different genera, based on wing pattern and male genitalia, but he also frequently grouped species by overall appearance. Lamas (2004) followed Forster ’ s arrangement, and retained in Splendeuptychia the species placed here in Argentaria gen.n., but shortly afterwards Murray and Prowell (2005) showed that, based on DNA sequence data, A. itonis comb.n. and S. ashna were distantly related. Subsequent molecular (Espeland et al., 2019a; Peña et al., 2010) and morphological (Huertas, 2014; Marín et al., 2017) phylogenetic studies have corroborated that discovery, including this study, which contains sequence data for all but three of the described species. The relationships of Argentaria gen.n. to other members of the ‘ Amphidecta clade’ are not strongly resolved, but the numerous morphological differences that separate the genus from other genera within the clade, and the fact that its constituent species have universally been recognized as closely related for more than 150 years, support its recognition as a distinct genus. Argentaria Huertas & Willmott, gen.n. argyropsacas (Bryk, 1953), comb.n., stat.rev., was Splendeuptychia [treated as a synonym of " Splendeuptychia " telesphora by Lamas (2004), but ventral wing pattern is distinct] clementia (Butler, 1877), comb.n., was Splendeuptychia clorimena (Stoll, 1790), comb.n., was Splendeuptychia = boliviensis (Forster, 1964), comb.n., syn.n., was Splendeuptychia [wing pattern variation and DNA barcodes suggests this is a southern form of clorimena] cosmophila (Hübner, 1823), comb.n., was Splendeuptychia = argenteus (Swainson, 1823), comb.n., was Splendeuptychia hygina (Butler, 1877), comb.n., was Splendeuptychia itonis (Hewitson, 1862), comb.n., was Splendeuptychia jadea (Brévignon & Benmesbah, 2012), comb.n., was Splendeuptychia [Brévignon & Benmesbah (2012, Complément à l'inventaire des Satyrinae de Guyane (Lepidoptera: Nymphalidae), pp. 36-52, 4 pls., 1 tab. In: Lacomme, D. & L. Manil (Eds.), Lépidoptères de Guyane. Tome 7. Nymphalidae)] kendalli (L.D. Miller, 1978), comb.n., was Splendeuptychia libitina (Butler, 1870), comb.n., was Splendeuptychia pagyris (Godart, [1824]), comb.n., was Splendeuptychia = ava (Anken, 1998), comb.n., was Splendeuptychia quadrina (Butler, 1869), comb.n., was Splendeuptychia salvini (Butler, 1867), comb.n., was Splendeuptychia telesphora (Butler, 1877), comb.n., was Splendeuptychia zischkai (Forster, 1964), comb.n., was Splendeuptychia

Cissia Doubleday, 1848 = Argyreuptychia Forster, 1964 anabelae (L.D. Miller, 1976) [Zhang et al. (2022, The Taxonomic Report of the International Lepidoptera Survey, 10(7): 1-60)] cheneyorum (Chermock, 1949) [Zhang et al. (2022, The Taxonomic Report of the International Lepidoptera Survey, 10(7): 1-60)] cleophes (Godman & Salvin, 1889) [Zhang et al. (2020, The Taxonomic Report of the International Lepidoptera Survey, 8(7): 1-40)] eous (Butler, 1867) [Zacca et al. (2018, Arthropod Systematics and Phylogeny, 76(2): 349-376)] = eoüs (Butler, 1867), missp. [Zacca et al. (2018, Arthropod Systematics and Phylogeny, 76(2): 349-376)] = kiliani (Anken, 1999) [Zacca et al. (2018, Arthropod Systematics and Phylogeny, 76(2): 349-376)] penelope (Fabricius, 1775) = clarissa (Cramer, 1780) = moneta (Weymer, 1911) phronius (Godart, [1824]) [Zacca et al. (2018, Arthropod Systematics and Phylogeny, 76(2): 349-376)] = punctatolineata (J. Zikán & W. Zikán, 1968), nom. nud. [Lamas, unpublished data] pompilia (C. Felder & R. Felder, 1867) = usitata (Butler, 1867) = pieria (Butler, 1867) = austera (Butler, 1867) [Zacca et al. (2018, Arthropod Systematics and Phylogeny, 76(2): 349-376)] = thelete (Snellen, 1887) proba (Weymer, 1911) = mariameliae (Hayward, 1957) pseudocleophes (L.D. Miller, 1976) [Zhang et al. (2022, The Taxonomic Report of the International Lepidoptera Survey, 10(7): 1-60)] rubricata (Edwards, 1871) [Zacca et al. (2018, Arthropod Systematics and Phylogeny, 76(2): 349-376)] - smithorum (Wind, 1946) [Zacca et al. (2018, Arthropod Systematics and Phylogeny, 76(2): 349-376)] wahala Grishin, 2022 [Zhang et al. (2022, The Taxonomic Report of the International Lepidoptera Survey, 10(7): 1-60)], Published as part of Espeland, Marianne, Nakahara, Shinichi, Zacca, Thamara, Barbosa, Eduardo P., Huertas, Blanca, Marín, Mario A., Lamas, Gerardo, Benmesbah, Mohamed, Brévignon, Christian, Casagrande, Mirna M., Fåhraeus, Christer, Grishin, Nick, Kawahara, Akito Y., Mielke, Olaf H. H., Miller, Jacqueline Y., Nakamura, Ichiro, Navas, Vanessa, Patrusky, Brooke, Pyrcz, Tomasz W., Richards, Lindsay, Tan, Denise, Tyler, Stephanie, Viloria, Angel, Warren, Andrew D., Xiao, Lei, Freitas, André V. L. & Willmott, Keith R., 2023, Combining target enrichment and Sanger sequencing data to clarify the systematics of the diverse Neotropical butterfly subtribe Euptychiina (Nymphalidae, Satyrinae), pp. 1-73 in Zoological Research 2023 on page 56, DOI: 10.1111/syen.12590, http://zenodo.org/record/7909395

Amiga Nakahara, Willmott & Espeland, 2019 arnaca (Fabricius, [1777]) [Nakahara et al. (2019, ZooKeys, 821: 85-152)] = ebusa (Cramer, 1780) [Nakahara et al. (2019, ZooKeys, 821: 85-152)] = arnaea (Fabricius, 1781), missp. = aranea (Fabricius, 1793), missp. = priamis (D’Almeida, 1922) [Nakahara et al. (2019, ZooKeys, 821: 85-152)] - adela (Nakahara & Espeland, 2019) [Nakahara et al. (2019, ZooKeys, 821: 85-152)] - indianacristoi (Nakahara & Marín, 2019), stat.rev. [raised from subspecies of A. arnaca to species by Orellana et al. (2020) based on unspecified morphological differences)/Orellana et al. (2020, Anartia, 29: 54-67)/Nakahara et al. (2019, ZooKeys, 821: 85-152)] sericeella (Bates, 1854) [Nakahara & Gallardo (2020, Tropical Lepidoptera Research, 29(2): 111-114)], Published as part of Espeland, Marianne, Nakahara, Shinichi, Zacca, Thamara, Barbosa, Eduardo P., Huertas, Blanca, Marín, Mario A., Lamas, Gerardo, Benmesbah, Mohamed, Brévignon, Christian, Casagrande, Mirna M., Fåhraeus, Christer, Grishin, Nick, Kawahara, Akito Y., Mielke, Olaf H. H., Miller, Jacqueline Y., Nakamura, Ichiro, Navas, Vanessa, Patrusky, Brooke, Pyrcz, Tomasz W., Richards, Lindsay, Tan, Denise, Tyler, Stephanie, Viloria, Angel, Warren, Andrew D., Xiao, Lei, Freitas, André V. L. & Willmott, Keith R., 2023, Combining target enrichment and Sanger sequencing data to clarify the systematics of the diverse Neotropical butterfly subtribe Euptychiina (Nymphalidae, Satyrinae), pp. 1-73 in Zoological Research 2023 on page 64, DOI: 10.1111/syen.12590, http://zenodo.org/record/7909395

Orotaygetis Nakahara & Zacca, 2018 surui Nakahara, Zacca & Lamas, 2018 [Nakahara et al. (2018, Insecta Mundi, 0639: 1-38)]

Taydebis Freitas, 2003 = Prenda Freitas & Mielke, 2011 clarissa (Freitas & Mielke, 2011) [Zacca et al. (2021, Zootaxa, 5023(4): 555-570)] guria Zacca, Casagrande & Mielke, 2021 [Zacca et al. (2021, Zootaxa, 5023(4): 555-570)] melobosis (Capronnier, 1874) [Zacca et al. (2021, Zootaxa, 5023(4): 555-570)] = peculiaris (Butler, 1874) [Zacca et al. (2021, Zootaxa, 5023(4): 555-570)] = fractifasciata (J. Zikán & W. Zikán, 1998), nom. nud., Published as part of Espeland, Marianne, Nakahara, Shinichi, Zacca, Thamara, Barbosa, Eduardo P., Huertas, Blanca, Marín, Mario A., Lamas, Gerardo, Benmesbah, Mohamed, Brévignon, Christian, Casagrande, Mirna M., Fåhraeus, Christer, Grishin, Nick, Kawahara, Akito Y., Mielke, Olaf H. H., Miller, Jacqueline Y., Nakamura, Ichiro, Navas, Vanessa, Patrusky, Brooke, Pyrcz, Tomasz W., Richards, Lindsay, Tan, Denise, Tyler, Stephanie, Viloria, Angel, Warren, Andrew D., Xiao, Lei, Freitas, André V. L. & Willmott, Keith R., 2023, Combining target enrichment and Sanger sequencing data to clarify the systematics of the diverse Neotropical butterfly subtribe Euptychiina (Nymphalidae, Satyrinae), pp. 1-73 in Zoological Research 2023 on page 65, DOI: 10.1111/syen.12590, http://zenodo.org/record/7909395

Atlanteuptychia Freitas, Barbosa & Mielke, 2013 ernestina (Weymer, 1911) [Freitas et al. (2013, Zoologia, 30: 661-668)]

Paramacera Butler, 1868 = Paramecera Butler, 1868, missp. allyni L.D. Miller, 1972 chinanteca L.D. Miller, 1972 copiosa L.D. Miller, 1972 xicaque (Reakirt [1867]) = epinephele (C. Felder & R. Felder, 1867) = conhiera Butler, 1868, nom. nud. rubrosuffusa L.D. Miller, 1972 [Zhang et al. (2022, The Taxonomic Report of the International Lepidoptera Survey, 10(7): 1-60)], Published as part of Espeland, Marianne, Nakahara, Shinichi, Zacca, Thamara, Barbosa, Eduardo P., Huertas, Blanca, Marín, Mario A., Lamas, Gerardo, Benmesbah, Mohamed, Brévignon, Christian, Casagrande, Mirna M., Fåhraeus, Christer, Grishin, Nick, Kawahara, Akito Y., Mielke, Olaf H. H., Miller, Jacqueline Y., Nakamura, Ichiro, Navas, Vanessa, Patrusky, Brooke, Pyrcz, Tomasz W., Richards, Lindsay, Tan, Denise, Tyler, Stephanie, Viloria, Angel, Warren, Andrew D., Xiao, Lei, Freitas, André V. L. & Willmott, Keith R., 2023, Combining target enrichment and Sanger sequencing data to clarify the systematics of the diverse Neotropical butterfly subtribe Euptychiina (Nymphalidae, Satyrinae), pp. 1-73 in Zoological Research 2023 on page 55, DOI: 10.1111/syen.12590, http://zenodo.org/record/7909395

Pseudeuptychia Forster, 1964 callichloris (Butler, 1867), comb.n., was Chloreuptychia [forms a well-supported clade with Pseudeuptychia languida, type species of Pseudeuptychia] cuzquenya Nakahara & Lamas, 2018 [Nakahara et al. (2018, Insecta Mundi, 0639: 1-38)] hemileuca (Staudinger, [1886]) herseis (Godart, [1824]), repl. name, comb.n., was Chloreuptychia [forms a well-supported clade with Pseudeuptychia languida, type species of Pseudeuptychia] = herse (Cramer, 1775), preocc. (not Hufnagel, 1766), comb.n., was Chloreuptychia = peruviana (J. Prüffer, 1922), comb.n., was Chloreuptychia = bellatula (D’Almeida, 1922), comb.n., was Chloreuptychia languida (Butler, 1871) - austrina Nakahara & Lamas, 2018 [Nakahara et al. (2018, Insecta Mundi, 0639: 1-38)] marica (Weymer, 1911), comb.n., was Chloreuptychia [forms a well-supported clade with Pseudeuptychia languida, type species of Pseudeuptychia] rectilinea (Brévignon, Rosant, Lamas & Willmott, 2019), comb.n., was Chloreuptychia [forms a well-supported clade with Pseudeuptychia languida, type species of Pseudeuptychia /Brévignon et al. (2019, Bulletin de la Société entomologique de France, 124(2): 127-138)], Published as part of Espeland, Marianne, Nakahara, Shinichi, Zacca, Thamara, Barbosa, Eduardo P., Huertas, Blanca, Marín, Mario A., Lamas, Gerardo, Benmesbah, Mohamed, Brévignon, Christian, Casagrande, Mirna M., Fåhraeus, Christer, Grishin, Nick, Kawahara, Akito Y., Mielke, Olaf H. H., Miller, Jacqueline Y., Nakamura, Ichiro, Navas, Vanessa, Patrusky, Brooke, Pyrcz, Tomasz W., Richards, Lindsay, Tan, Denise, Tyler, Stephanie, Viloria, Angel, Warren, Andrew D., Xiao, Lei, Freitas, André V. L. & Willmott, Keith R., 2023, Combining target enrichment and Sanger sequencing data to clarify the systematics of the diverse Neotropical butterfly subtribe Euptychiina (Nymphalidae, Satyrinae), pp. 1-73 in Zoological Research 2023 on pages 63-64, DOI: 10.1111/syen.12590, http://zenodo.org/record/7909395

Koutalina Viloria & Murienne, 2021 pamela (Hayward, 1957) [Benmesbah et al. (2021, Anartia, 31: 7-62)]

Trico tricolor tricolor (Hewitson, 1850), comb.n. Euptychia tricolor Hewitson (1850, p. 440). TL: river Amazon [Pará, Brazil]. Types: LT male (here designated): ‘ BMNH (E)-1,266,952//Type//B. M. TYPE No. Rh. 3183 Euptychia tricolor ♂ Hew// Para. Hewitson Coll. 79 – 69. Euptychia Tricolor. Hew. 1’. (NHMUK) [figured on www.butterfliesofamerica.com, examined]. BRAZIL: Amapá: Serra do Navio (ICOMI), [0°59'N, 52°3'W], 14 Sep 1963, 1 ♀, (DZUP); Amazonas: 78 km W Manaus, Rio Preto de Eva, 100 m, (Büche, M.), Dec 1996, 1 ♀ [MUSM-LEP-103501], 1 ♀ [MUSM-LEP-103502], (MUSM); Camuna, (Le Moult, E.), 1 ♁ [FLMNH-MGCL-266051], (FLMNH); Manaus, [3°7'S, 60°2'W], (Le Moult, E.), 1 ♁ [FLMNH-MGCL-266043], 1 ♁ [FLMNH-MGCL-266047], 1 ♁ [FLMNH-MGCL-266048], 1 ♁ [FLMNH- MGCL-266049], (FLMNH), (Moss, A. M.), 1 ♀ [BMNH (E)-525460], (NHMUK); Manaus, Reserva Ducke, [2°53'S, 59°57'W], (Hutchings, R. W., Sullivan, J. B.), 13 Dec 1993, 1 ♁ [FLMNH-MGCL-266065], (FLMNH); Maués, [3°22'S, 57°43'W], Nov 1998, 1 ♁ [FLMNH-MGCL-266061], (FLMNH), (Balint), 1 ♁, (DZUP), (Le Moult, E.), 1 ♁ [FLMNH-MGCL-266044], 1 ♁ [FLMNH-MGCL-266045], 1 ♁ [FLMNH-MGCL-266050], 1 ♁ [FLMNH-MGCL-266062], 1 ♁ [FLMNH-MGCL-266063], 1 ♁ [FLMNH-MGCL-266064], (FLMNH); ' São Paulo de Olivença' - (error), (Moss, A. M.), 1 ♀ [BMNH (E)- 525449], 1 ♀ [BMNH (E)- 525451], (NHMUK); Pará: [Rio] Tapajós, [4°16'8''S, 55°59'10''W], 25 m, 1 ♀ [BMNH (E)- 1668489], (NHMUK), (Bates, H. W.), 1 ♁ [BMNH (E)- 1668486], (NHMUK), 3 Oct 2012, 1 ♁, (ZUEC), 4 Oct 2012, 1 ♁, (ZUEC), 8 Dec 2012, 1 ♁, (ZUEC); 15 km S Itaituba, [4°17'S, 56°5'W], (Callaghan, C. J.), 23 Jul 1978, 1 ♁ [FLMNH-MGCL-266054], (FLMNH); Amazonas, (Fassl, A. H.), (ZSM); Belém, Utinga, [1°27'S, 48°25'W], Feb 1957, 1 ♁, (DZUP); Rio Cumina, Igarapé dos Indios, 13 Oct 1936, 1 ♁, (DZUP); Itaituba on Rio Tapajós, [4°16'8''S, 55°59'10''W], (Le Moult, E.), 1 ♁ [FLMNHMGCL-266052], 1 ♁ [FLMNH-MGCL-266060], (FLMNH); Óbidos, [1°54'S, 55°31'W], (Le Moult, E.), 1 ♁ [FLMNH-MGCL-266053], 1 ♁ FLMNHMGCL-266055], 1 ♁ [FLMNH-MGCL-266056], 1 ♀ [FLMNH-MGCL-266059], (FLMNH); Pará, [1°0'S, 51°11'W], 1 ♁ [BMNH (E)- 1266952], 1 ♁ [BMNH (E)- 1668482], 1 ♁ [BMNH (E)- 1668483], 1 ♁ [BMNH (E)- 1668485], (NHMUK), 15 Mar 1893, (ZSM), 1 ♀, (ZSM), (Bates, H. W.), 1 ♁ [BMNH (E)- 1668484], (NHMUK), (Erhardt), (ZSM), (Mathan, M. de), 1 ♁ [BMNH (E)- 1668480], 1 ♁ [BMNH (E)- 1668481], (NHMUK), (Moss, A. M.), 1 ♁ [BMNH (E)- 1499285], 1 ♁ [BMNH (E)- 525595], 1 ♁ [BMNH (E)- 525596], 1 ♁ [BMNH (E)- 525603], 1 ♁ [BMNH (E)- 525605], (NHMUK); Rio Tapajós, [4°16'8''S, 55°59' 10''W], 25 m, (Bates, H. W.), 1 ♁ [BMNH (E)- 1668487], (NHMUK), (Klug, G. G.), Sep 1931, 1 ♁ [BMNH (E)- 1499283], 1 ♁ [BMNH (E)- 1499284], (NHMUK); Santarém, [2°26'S, 54°43'W], (Le Moult, E.), 1 ♀ [FLMNH-MGCL-266057], 1 ♀ [FLMNH-MGCL-266058], (FLMNH); Santa Bárbara do Pará, (Carneiro, E., Dolibaina, D., Dias, F., Moreira), 2-3 Feb 2010, 1 ♁, (DZUP), 6 Feb 2010, 1 ♁, (DZUP); Tapará, [2°2'S, 49°36'W], (Le Moult, E.), 1 ♁ [FLMNH-MGCL-266249], (FLMNH); Taperinha, [0°52' S,47°49'W], (Le Moult, E.), 1 ♁ [FLMNH-MGCL-266046], (FLMNH). FRENCH GUIANA: Cayenne: Approuage River, 10 mi W Regina, vicinity of St Anthanase Lodge, [4°11'10''N, 52°20'8''W], 120 m, (Brock, J.), 14-17 Oct 1990, 2 ♁, (BME); Cayenne: Cacao, [4°35' 51''N, 52°26'11''W], 0-150 m, (Harris, L. N.), 6 May 1998, 1 ♁ [FLMNH-MGCL-266088; Streams-falls-forest], (FLMNH); Cayenne, [4°56'N, 52°20'W], 1 ♁ [BMNH (E)- 1499279], 1 ♁ [BMNH (E)- 1499280], 1 ♁ [BMNH (E)- 1499281], 1 ♁ [BMNH (E)- 1668505], 1 ♁ [BMNH (E)- 1668507], 1 ♀ [BMNH (E)- 1668513], (NHMUK), (Bar, C.), 1 ♁ [BMNH (E)- 1668508], (NHMUK); St-Laurent du Maroni: Aloike-Maripasoula, [3°39'22''N, 53°59' 4''W], 110 m, (Brévignon, C.), 6 Apr 1987, 1 ♁ [MUSM-LEP-103500], (MUSM); Maroni River, (Le Moult, E.), 1 ♁ [FLMNH-MGCL-266082; dissection, KW-14-015], 1 ♁ [FLMNH-MGCL-266083], 1 ♁ [FLMNH-MGCL-266084], 1 ♁ [FLMNH-MGCL-266085], 1 ♁ [FLMNH-MGCL-266086], 1 ♁ [FLMNH-MGCL-266087], 1 ♀ [FLMNH-MGCL-266089], 1 ♀ [FLMNH-MGCL-266090], (FLMNH); Maroni river, Maripasoula, [3°41'N, 54°2'W], (Brévignon, C.), 3 Mar 1987, 1 ♁ [MUSM-LEP-103499], (MUSM); Plateau Mines, Moutouchi Lodge, [5°19'47''N, 54°4'1''W], 45 m, (Sourakov, A.), 1-5 Mar 2013, 1 ♀ [FLMNH-MGCL-209668], (FLMNH); St. Laurent du Maroni, [5°30'N, 54°2'W], 1923, 1 ♁ [BMNH (E)- 1668510], (NHMUK), Jul-Sep 1915, 1 ♁ [BMNH (E)- 1668509], (NHMUK), Jun, 1 ♁ [BMNH (E)-1499282], (NHMUK), (Moult), Nov, 1 ♁ [BMNH (E)- 1668511], (NHMUK); Not located: ‘ French Guiana’, (Bar, C.), 1 ♁ [BMNH (E)- 1668506], (NHMUK). GUYANA: Cuyuni-Mazaruni: Bartica, [6°24'N, 58°37'W], Mar 1939, 1 ♁, (BMB); junction of Cuyuni and Arimu rivers, 30 m, (Fratello, S.), 2 Oct 1991, 1 ♁ [FLMNH-MGCL-266076], (FLMNH); junction of Cuyuni and Arimu rivers, 46 m, (Fratello, S.), 28 Sep 1991, 1 ♀ [FLMNH-MGCL-266072], (FLMNH); East Berbice-Corentyne: Confluence of Oronoque and New River, [2°45'8''N, 57°26'5''W], (Hudson, C. A.), 20 Aug-20 Sep 1937, 1 ♁ [BMNH (E)- 1499271], (NHMUK); ' Kutari [River] Sources', [1°58'N, 56°36'W], (Hudson, C. A.), Jan-Feb 1936, 1 ♁ [BMNH (E)- 1668492], (NHMUK); Upper Demerara-Berbice: Essequibo River, 35 mi SW of Georgetown, Shanklands Resort, [6°28'44''N, 58°34' 54''W], 20 m, (Douglas, M. G.), 20-28 Sep 2006, 1 ♁ [FLMNH-MGCL-266074], 1 ♁ [FLMNH-MGCL-266075], 1 ♀ [FLMNHMGCL-266073], 1 ♀ [FLMNH-MGCL-266078], 1 ♀ [FLMNH-MGCL-266080], 1 ♀ [FLMNH-MGCL-266081], (FLMNH); Not located: ‘ Guyana’, 1 ♁ [BMNH (E)- 1499272], 1 ♁ [BMNH (E)- 1668493], 1 ♁ [BMNH (E)- 1668495], (NHMUK); Demerara, [6°47'N, 58°10'W], (Castell), 1 ♁ [BMNH (E)- 1668491], 1 ♁ [BMNH (E)- 1668494], (NHMUK); Essequibo River, Moraballi Creek, 10 Nov 1929, 1 ♁ [BMNH (E)- 1499270], (NHMUK); Potaro River, 1 ♀ [FLMNH-MGCL-266070], (FLMNH), (Roberts, C. B.), 12 Jul 1902, 1 ♁ [FLMNH-MGCL-266067], (FLMNH), 17 Jul 1902, 1 ♁ [FLMNH-MGCL-266068], 1 ♀ [FLMNH-MGCL-266069], (FLMNH), Jul 1902, 1 ♀ [FLMNH-MGCL-266079], (FLMNH), Oct-Nov 1902, 1 ♁ [FLMNH-MGCL-266066], (FLMNH); Río Demerara, 1 ♁ [BMNH (E)- 1499267], 1 ♁ [BMNH (E)- 1499268], 1 ♁ [BMNH (E)- 1499269], 1 ♁ [BMNH (E)- 1668490], (NHMUK); Suruwabaru CK, Mt. Wokamung, 680-690 m, (Fratello, S.), Nov, 1 ♀ [FLMNH-MGCL-266071], (FLMNH); Suruwabaru CK, Mt. Wokamung, 686 m, (Fratello, S.), Nov, 1 ♀ [FLMNH-MGCL-266077], (FLMNH). SURINAME: Brokopondo: Berg-en-Dal, [5°9'N, 55°4'W], (Ellacombe, C. W.), May 1892, 1 ♁ [BMNH (E)- 1668496], (NHMUK), (Ellacombe, G. W.), May 1892, 1 ♁ [BMNH (E)- 1499273], 1 ♁ [BMNH (E)- 1499275], 1 ♁ [BMNH (E)- 1499277], (NHMUK); Marowijne: Río Lawa, Anapaika, [3°25'N, 54°1'W], (Malkin, B.), 27 Nov 1963, 1 ♁ [MUSM-LEP-103498], (MUSM); Not located: ‘ Surinam’, 1 ♁ [BMNH (E)- 1668497], 1 ♁ [BMNH (E)- 1668498], 1 ♁ [BMNH (E)- 1668499], 1 ♁ [BMNH (E)- 1668500], 1 ♁ [BMNH (E)- 1668502], 1 ♁ [BMNH (E)- 1668503], 1 ♁ [BMNH (E)- 1668504], 1 ♁ [BMNH (E)- 1668514], (NHMUK), (Ellacombe, G. W.), 1 ♁ [BMNH (E)- 1499276], (NHMUK); 'interior Surinam', Sep 1892, 1 ♁ [BMNH (E)- 1499278], (NHMUK), (Ellacombe, C. W.), Aug 1892, 1 ♁ [BMNH (E)- 1668501], (NHMUK), (Ellacombe, G. W.), Sep 1892, 1 ♁ [BMNH (E)- 1499274], (NHMUK). TRINIDAD & TOBAGO: Not located: ‘Trinidad’, [10°26'17''N, 61°15'12''w], 1 ♁ [BMNH (E)- 1668512], (NHMUK). VENEZUELA: Bolívar: El Dorado - Sta Elena, km 83, [6°9'59''N, 61°25' 37''W], 160 m, (Harris, L. & H.), 27 Jun 1984, 1 ♀ [FLMNH-MGCL-266042; km. 82], (FLMNH), (Lichy, R.), 18 Feb 1966, 1 ♁ [FLMNH-MGCL-266041; km. 82], (FLMNH). Country unknown: Not located: ' Amazon', (Bates, H. W.), 1 ♁ [BMNH (E)- 1668488], (NHMUK); 'Amazonas', (Fassl, A. H.), 1 ♁ [BMNH (E)- 1499286], (NHMUK); no data, 1 ♁ [BMNH (E)- 1499287], 1 ♁ [BMNH (E)- 1499288], 1 ♁ [BMNH (E)- 1499289], 1 ♁ [BMNH (E)- 1499290], (NHMUK) Other records: VENEZUELA: Bolívar: Río Grande, 90 km N El Callao, [7°56'54''N, 62°18'6''W], 100 m, (Neild, A. F. E.), 23 Oct 2000, 1 ♁, (ANNE) (Neild, A. (12 Aug 2020, pers. comm. to KRW by email with images))., Published as part of Espeland, Marianne, Nakahara, Shinichi, Zacca, Thamara, Barbosa, Eduardo P., Huertas, Blanca, Marín, Mario A., Lamas, Gerardo, Benmesbah, Mohamed, Brévignon, Christian, Casagrande, Mirna M., Fåhraeus, Christer, Grishin, Nick, Kawahara, Akito Y., Mielke, Olaf H. H., Miller, Jacqueline Y., Nakamura, Ichiro, Navas, Vanessa, Patrusky, Brooke, Pyrcz, Tomasz W., Richards, Lindsay, Tan, Denise, Tyler, Stephanie, Viloria, Angel, Warren, Andrew D., Xiao, Lei, Freitas, André V. L. & Willmott, Keith R., 2023, Combining target enrichment and Sanger sequencing data to clarify the systematics of the diverse Neotropical butterfly subtribe Euptychiina (Nymphalidae, Satyrinae), pp. 1-73 in Zoological Research 2023 on pages 34-71, DOI: 10.1111/syen.12590, http://zenodo.org/record/7909395, {"references":["Hewitson, W. C. (1850) Descriptions of some new species of butterflies. Annals and Magazine of Natural History, Second Series, 6, 434 - 440."]}

Optimandes Marín, Nakahara & Willmott, 2019 eugenia (C. Felder & R. Felder, 1867) [Willmott et al. (2019, Tropical Lepidoptera Research, 29(1): 29-44)] = phineus (Butler, 1867) [Willmott et al. (2019, Tropical Lepidoptera Research, 29(1): 29-44)] - transversa (Weymer, 1911) [Willmott et al. (2019, Tropical Lepidoptera Research, 29(1): 29-44)] mocha Willmott, J. Hall & Lamas, 2019 [Willmott et al. (2019, Tropical Lepidoptera Research, 29(1): 29-44)], Published as part of Espeland, Marianne, Nakahara, Shinichi, Zacca, Thamara, Barbosa, Eduardo P., Huertas, Blanca, Marín, Mario A., Lamas, Gerardo, Benmesbah, Mohamed, Brévignon, Christian, Casagrande, Mirna M., Fåhraeus, Christer, Grishin, Nick, Kawahara, Akito Y., Mielke, Olaf H. H., Miller, Jacqueline Y., Nakamura, Ichiro, Navas, Vanessa, Patrusky, Brooke, Pyrcz, Tomasz W., Richards, Lindsay, Tan, Denise, Tyler, Stephanie, Viloria, Angel, Warren, Andrew D., Xiao, Lei, Freitas, André V. L. & Willmott, Keith R., 2023, Combining target enrichment and Sanger sequencing data to clarify the systematics of the diverse Neotropical butterfly subtribe Euptychiina (Nymphalidae, Satyrinae), pp. 1-73 in Zoological Research 2023 on page 65, DOI: 10.1111/syen.12590, http://zenodo.org/record/7909395

Emeryus Zacca, Casagrande & Mielke, 2020 argulus (Godart, [1824]), repl. name [Zacca et al. (2020, Austral Entomology, 59: 505-523)] = argante (Cramer, 1779), preocc. (not Fabricius, 1775) [Zacca et al. (2020, Austral Entomology, 59: 505-523)] = huebneri (Butler, 1867) [Zacca et al. (2020, Austral Entomology, 59: 505-523)] - magnum Zacca, Casagrande & Mielke, 2020 [Zacca et al. (2020, Austral Entomology, 59: 505-523)] difficilis (Forster, 1964) [Zacca et al. (2020, Austral Entomology, 59: 505-523)] numeria (C. Felder & R. Felder, 1867) [Zacca et al. (2020, Austral Entomology, 59: 505-523)] = ambigua (Butler, 1867) [Zacca et al. (2020, Austral Entomology, 59: 505-523)] = historie (Weymer, 1911), nom. nud. [Zacca et al. (2020, Austral Entomology, 59: 505-523)]

Scriptor Nakhara & Espeland, 2020 sphenophorus Lamas & Nakahara, 2020 [Nakahara et al. (2020, PeerJ, DOI: 10.7717/peerj.10324)], Published as part of Espeland, Marianne, Nakahara, Shinichi, Zacca, Thamara, Barbosa, Eduardo P., Huertas, Blanca, Marín, Mario A., Lamas, Gerardo, Benmesbah, Mohamed, Brévignon, Christian, Casagrande, Mirna M., Fåhraeus, Christer, Grishin, Nick, Kawahara, Akito Y., Mielke, Olaf H. H., Miller, Jacqueline Y., Nakamura, Ichiro, Navas, Vanessa, Patrusky, Brooke, Pyrcz, Tomasz W., Richards, Lindsay, Tan, Denise, Tyler, Stephanie, Viloria, Angel, Warren, Andrew D., Xiao, Lei, Freitas, André V. L. & Willmott, Keith R., 2023, Combining target enrichment and Sanger sequencing data to clarify the systematics of the diverse Neotropical butterfly subtribe Euptychiina (Nymphalidae, Satyrinae), pp. 1-73 in Zoological Research 2023 on page 69, DOI: 10.1111/syen.12590, http://zenodo.org/record/7909395

Trico Nakahara & Espeland, genus novum. Type species — Euptychia tricolor Hewitson, 1850, by present designation. Zoobank registration: https://zoobank.org/Nomenclatural Acts/1EB03CDD-C7B3-4AB0-9920-CC59642A4353 Systematic placement and diagnosis. Trico gen.n. is a member of the so-called ‘ Splendeuptychia clade’, and it is weakly supported as sister to Omacha (SH-aLRT/UFBoot = 52.3/62, Figure 10), with these two taxa being rather distantly related to the remainder of the clade. This genus was not included in Espeland et al. (2019a). Nevertheless, both Trico gen.n. and Omacha are monotypic genera, and both accommodate distinctive euptychiine species that do not resemble each other, or other euptychiine genera. Males of Trico gen.n. are distinguished from virtually all euptychiine species by the combination of their iridescent blue scales covering DHW cells Cu 2 and 2A, which also traverse up along the outer margin towards apex, coupled with orangish area anterior of DHW M 2 (Figures 26 and 27). Although lilac-blue scales are present in a similar area in some male euptychiine species (e.g. Chloreuptychia chlorimene, Lazulina tolumnia comb.n.), these species never possess orangish colouration at the anterior region of DHW. On the other hand, female specimens of Trico gen.n. can closely resemble some euptychiine taxa, perhaps phenotypically being most similar to Satyrotaygetis iris comb.n., despite being distantly related. The male of S. iris is easily distinguished from female specimens of Trico gen.n. by its androconial scales at the distal side of DHW discal cell extending slightly along M 3 and Cu 1, as well as presence of greyish long setiform scales in the discal cell, which are both absent in the female of Trico gen.n. Female specimens of Trico gen.n. are distinguished from females of S. iris comb.n. by having a smoother VHW submarginal band in cell Cu 2, which usually bends inwards in S. iris comb.n. The females of these two taxa can be further distinguished by the membranous lamella antevaginalis of specimens of Trico gen.n. (Figure 28c; sclerotized in S. iris) and ductus seminalis exiting from the ductus bursae closer to the corpus bursae in specimens of Trico gen.n. (Figure 28d; origin of ductus bursae close to ostium bursae in S. iris comb.n.). Etymology. The generic name is based on the Latin word ‘trico’, which is a masculine noun in the nominative singular, meaning ‘mischief-maker’ or ‘trickster’, in reference to the remarkable sexual dimorphism of this species. Description (Figures 26 – 28). Some notable characters include: eyes naked; pterothoracic legs dorsally darker, tibia with two principal longitudinal rows of spines ventrally, pair of short spurs of similar length at distal end of tibia, first tarsomere with three principal longitudinal rows of spines ventrally until distal end, distal end of first tarsomere and remaining distal tarsomeres with four principal longitudinal rows of spines ventrally. Medium-sized Euptychiina (FW length typically 21 – 25 mm). Sexes dimorphic. Male: DHW with light yellowish long hair-like scales at base of discal cell, somewhat at posterior edge of orangish area; greyish long hair-like scales visible in cell Cu 2, area between postdiscal band and submarginal band, along 2A; greyish androconial patch present in adjacent area of cell 2A in male, otherwise wing shape and pattern as illustrated (Figures 26 and 27). Male genitalia with cornuti absent, otherwise as illustrated (Figure 28). Female: DFW and DHW with purple lilac sheen; otherwise as illustrated (Figures 26 and 27). Female abdomen with intersegmental membrane of 7th and 8th abdominal segment not pleated and expandable (Figure 28); genitalia with lamella antevaginalis membranous; ductus bursae membranous, pair of signa present on corpus bursae. Trico Nakahara & Espeland, gen.n. tricolor (Hewitson, 1850), comb.n., was Magneuptychia - fulgora (Butler, 1869), comb.n., was Magneuptychia, Published as part of Espeland, Marianne, Nakahara, Shinichi, Zacca, Thamara, Barbosa, Eduardo P., Huertas, Blanca, Marín, Mario A., Lamas, Gerardo, Benmesbah, Mohamed, Brévignon, Christian, Casagrande, Mirna M., Fåhraeus, Christer, Grishin, Nick, Kawahara, Akito Y., Mielke, Olaf H. H., Miller, Jacqueline Y., Nakamura, Ichiro, Navas, Vanessa, Patrusky, Brooke, Pyrcz, Tomasz W., Richards, Lindsay, Tan, Denise, Tyler, Stephanie, Viloria, Angel, Warren, Andrew D., Xiao, Lei, Freitas, André V. L. & Willmott, Keith R., 2023, Combining target enrichment and Sanger sequencing data to clarify the systematics of the diverse Neotropical butterfly subtribe Euptychiina (Nymphalidae, Satyrinae), pp. 1-73 in Zoological Research 2023 on pages 32-67, DOI: 10.1111/syen.12590, http://zenodo.org/record/7909395, {"references":["Hewitson, W. C. (1850) Descriptions of some new species of butterflies. Annals and Magazine of Natural History, Second Series, 6, 434 - 440.","Espeland, M., Breinholt, J., Barbosa, E. P., Casagrande, M., Huertas, B., Lamas, G. et al. (2019 a) Four hundred shades of brown: higher level phylogeny of the problematic Euptychiina (Lepidoptera, Nymphalidae, Satyrinae) based on hybrid enrichment data. Molecular Phylogenetics and Evolution, 131, 116 - 124.","Butler, A. G. (1869) Lepidoptera Exotica, or descriptions and illustrations of exotic Lepidoptera. London: E. W. Janson, p. 339."]}

Scriptor Nakhara & Espeland, 2020 sphenophorus Lamas & Nakahara, 2020 [Nakahara et al. (2020, PeerJ, DOI: 10.7717/peerj.10324)]

Euptychoides Forster, 1964 albofasciata (Hewitson, 1869) inani (Staudinger, [1886]), comb.n., was Macrocissia [Andrade et al. (2019) placed this species in Macrocissia, but it does not cluster with the type species of that genus, instead being strongly supported by molecular data as a member of a clade that includes the type species of Euptychoides] = juani (Staudinger, 1887), missp., comb.n., was Macrocissia laccine (C. Felder & R. Felder, 1867) = saturnus (Butler, 1867), syn.n. [number of pupils in VHW ocelli is variable even between wings of the same individual] pseudosaturnus Forster, 1964, Published as part of Espeland, Marianne, Nakahara, Shinichi, Zacca, Thamara, Barbosa, Eduardo P., Huertas, Blanca, Marín, Mario A., Lamas, Gerardo, Benmesbah, Mohamed, Brévignon, Christian, Casagrande, Mirna M., Fåhraeus, Christer, Grishin, Nick, Kawahara, Akito Y., Mielke, Olaf H. H., Miller, Jacqueline Y., Nakamura, Ichiro, Navas, Vanessa, Patrusky, Brooke, Pyrcz, Tomasz W., Richards, Lindsay, Tan, Denise, Tyler, Stephanie, Viloria, Angel, Warren, Andrew D., Xiao, Lei, Freitas, André V. L. & Willmott, Keith R., 2023, Combining target enrichment and Sanger sequencing data to clarify the systematics of the diverse Neotropical butterfly subtribe Euptychiina (Nymphalidae, Satyrinae), pp. 1-73 in Zoological Research 2023 on page 64, DOI: 10.1111/syen.12590, http://zenodo.org/record/7909395

Cyllopsis clade The ‘ Cyllopsis clade’ was recognized in Espeland et al. (2019a), where it was placed as a strongly supported sister group to a much larger clade including major, species-rich clades such as the ‘ Splendeuptychia clade’, ‘ Taygetis clade’, ‘ Megisto clade’, ‘ Pareuptychia clade’. The clade was similarly recovered in previous molecular phylogenetic studies (Murray & Prowell, 2005; Nakahara, Janzen, et al., 2015; Peña et al., 2010), and in the recent study of Rosa et al. (2021). Currently, four genera are recognized in the ‘ Cyllopsis clade’, namely Cyllopsis (30 species), Paramacera (5 species), Inbio (monotypic) and Atlanteuptychia (monotypic), and our molecular data suggest further taxonomic changes at the generic level are not needed (Figures 3, S 2 and S 3). The relationships between all genera are stable and well-supported in all analyses, with Atlanteuptychia being sister to the remainder of the clade, Inbio being sister to Paramacera, and these two again being sister to Cyllopsis. Thus, the generic classification is perhaps the most stable in comparison with other clades in the subtribe that contain multiple genera. Based on our unpublished data, the only known undescribed species within this clade are in Cyllopsis. Only two Cyllopsis species have been described more recently, including the unique Cyllopsis emilia, which appears to be one of the few euptychiine species that may be involved in mimicry with Pieridae butterflies (Chacon & Nishida,2002; Warren et al., 2018). Conversely, there are likely several currently recognized Cyllopsis species that may represent seasonal forms, so some revision to the species taxonomy is likely needed (Warren, unpublished data). Members of the ‘ Cyllopsis clade’ are relatively small butterflies, with the forewing length of most species not exceeding 25 mm. Possible synapomorphies (not unique) and distinctive characters for the clade include the following: (a) brachia short (about half of uncus in length or shorter),described as ‘not freely articulated’ in Miller (1974); (b) smooth vesica lacking obvious sclerotized cornuti. Unlike other clades in the subtribe, members of the ‘ Cyllopsis clade’ are most diverse in Central America, especially in southern Mexico and Guatemala. In fact, the monotypic genus Atlanteuptychia is the only taxon in this clade found east of the Andes, namely from the Atlantic Forest of Brazil (Freitas et al., 2013), resulting in a disjunct distribution for the clade. Habitat preferences of species in this clade range from lowland rainforest to cloud forest at over 2000 m, with Cyllopsis being one of only three Euptychiina genera to have diversified extensively in montane regions (the others are Forsterinaria and Moneuptychia). The immature stages have been described for Inbio hilara feeding on Rhipidocladum (Poaceae: Bambusoideae: Bambuseae) (Nakahara,Janzen, et al., 2015), and various Cyllopsis species have been reported feeding on bamboo and other grass genera (Beccaloni et al., 2008), but otherwise there are few comprehensive, detailed descriptions or hostplant records for most species in the clade., Published as part of Espeland, Marianne, Nakahara, Shinichi, Zacca, Thamara, Barbosa, Eduardo P., Huertas, Blanca, Marín, Mario A., Lamas, Gerardo, Benmesbah, Mohamed, Brévignon, Christian, Casagrande, Mirna M., Fåhraeus, Christer, Grishin, Nick, Kawahara, Akito Y., Mielke, Olaf H. H., Miller, Jacqueline Y., Nakamura, Ichiro, Navas, Vanessa, Patrusky, Brooke, Pyrcz, Tomasz W., Richards, Lindsay, Tan, Denise, Tyler, Stephanie, Viloria, Angel, Warren, Andrew D., Xiao, Lei, Freitas, André V. L. & Willmott, Keith R., 2023, Combining target enrichment and Sanger sequencing data to clarify the systematics of the diverse Neotropical butterfly subtribe Euptychiina (Nymphalidae, Satyrinae), pp. 1-73 in Zoological Research 2023 on page 8, DOI: 10.1111/syen.12590, http://zenodo.org/record/7909395, {"references":["Espeland, M., Breinholt, J., Barbosa, E. P., Casagrande, M., Huertas, B., Lamas, G. et al. (2019 a) Four hundred shades of brown: higher level phylogeny of the problematic Euptychiina (Lepidoptera, Nymphalidae, Satyrinae) based on hybrid enrichment data. Molecular Phylogenetics and Evolution, 131, 116 - 124.","Murray, D. & Prowell, D. P. (2005) Molecular phylogenetics and evolutionary history of the neotropical Satyrine subtribe Euptychiina (Nymphalidae: Satyrinae). Molecular Phylogenetics and Evolution, 34, 67 - 80.","Pena, C., Nylin, S., Freitas, A. V. L. & Wahlberg, N. (2010) Biogeographic history of the butterfly subtribe Euptychiina (Lepidoptera, Nymphalidae, Satyrinae). Zoologica Scripta, 39, 243 - 258.","Rosa, A. H. B., Huertas, B., Willmott, K. R., Barbosa, E. P., Machado, P. A., Mielke, O. H. H. et al. (2021) Fifty years without a name: a new species of Splendeuptychia Forster (Lepidoptera: Nymphalidae: Satyrinae). Zootaxa, 5061, 95 - 114.","Chacon, I. & Nishida, K. (2002) A new species of Cyllopsis (Lepidoptera: Nymphalidae: Satyrinae) from Costa Rica. Revista de Biologia Tropical, 50, 679 - 683.","Warren, A. D., Nakahara, S., Llorente-Bousquets, J., Luis-Martinez, A. & Miller, J. Y. (2018) A new species of Cyllopsis R. Felder, 1869 from the highlands of Chiapas, Mexico (Lepidoptera: Nymphalidae: Satyrinae). Zootaxa, 4403, 570 - 577.","Miller, L. D. (1974) Revision of the Euptychiini (Satyridae) 2. Cyllopsis R. Felder. Bulletin of the Allyn Museum, 20, 1 - 98.","Freitas, A. V. L., Barbosa, E. P., Santos, J. P. & Mielke, O. H. H. (2013) A new genus, Atlanteuptychia gen. Nov., for Euptychia Ernestina (Lepidoptera: Nymphalidae: Satyrinae). Zoologia (Curitiba), 30, 661 - 668.","Beccaloni, G. W., Viloria, A. L., Hall, S. K. & Robinson, G. S. (2008) Catalogue of the hostplants of the Neotropical butterflies. Monografias Tercer Milenio. Sociedad Entomologica´Aragonesa (SEA) / Red Iberoamericana de Biogeografia y Entomologia Sistematica (RIBES) / Ciencia y Tecnologia para el Desarrollo (CYTED) / Natural History Museum, London, U. K. (NHM) / Instituto Venezolano de Investigaciones Cientificas, Venezuela (IVIC), Zaragoza, p. 536."]}

Caeruleuptychia Forster, 1964 = Weymerana Forster, 1964 aegrota (Butler, 1867) aetherialis (Butler, 1877) [Nakahara et al. (2017, Insect Systematics and Evolution, 49(2): 130-182)] coelestis (Butler, 1867) coelica (Hewitson, 1869) cyanites (Butler, 1871) = stigmatica (Godman, 1905) divina (Weymer, 1911) francisca (Butler, 1870) [Nakahara et al. (2020, Tijdschrift voor Entomologie, 163: 51-61)] glauca (Weymer, 1911) helena (Anken, 1994) helios (Weymer, 1911) = caelestis Brévignon, 2008 [Brévignon (2008, Inventaire des Satyrinae de Guyane française (Lepidoptera: Nymphalidae), pp. 62- 94, 7 pls., 2 figs. In: Lacomme, D. & L. Manil (Eds.), Lépidoptères de Guyane. Tome 3. Rhopalocères 2)] = caelestissima Brévignon, 2010, repl. name [Nakahara et al. (2017, Insect Systematics and Evolution, 49(2): 130-182)] = keltoumae (Brévignon & Benmesbah, 2012) [Nakahara et al. (2017, Insect Systematics and Evolution, 49(2): 130-182)] lobelia (Butler, 1870) mare (Butler, 1869) maryzenderae Lamas & Nakahara, 2017 [Nakahara et al. (2017, Insect Systematics and Evolution, 49(2): 130-182)] penicillata (Godman, 1905) pilata (Butler, 1867) romani (Aurivillius, 1929), comb.n., was Cepheuptychia [preliminary DNA sequence data suggest that this species should provisionally be placed in Caeruleuptychia (Barbosa, unpublished data)] saul Brévignon & Benmesbah, 2012 [Brévignon & Benmesbah (2012, Complément à l'inventaire des Satyrinae de Guyane (Lepidoptera: Nymphalidae), pp. 36-52, 4 pls., 1 tab. In: Lacomme, D. & L. Manil (Eds.), Lépidoptères de Guyane. Tome 7. Nymphalidae)] scopulata (Godman, 1905) = marisea (Dyar, 1914) = susanna (Hayward, 1957) scripta Nakahara, Zacca & Huertas, 2017 [Nakahara et al. (2017, Insect Systematics and Evolution, 49(2): 130-182)] tenera (Weymer, 1911) thaliana Nakahara & Piovesan, 2022 [Nakahara et al. (2023, Tropical Lepidoptera Research, 33(1): 23-36)] trembathi Willmott, Nakahara, J. Hall & Neild, 2017 [Nakahara et al. (2017, Insect Systematics and Evolution, 49(2): 130-182)] twalela Brévignon, 2005 [Brévignon (2005, Lambillionea, 105(3)(1): 393-404)] umbrosa (Butler, 1870) = viridicans (Weymer, 1911) urania (Butler, 1867) = caerulea (Butler, 1869) [Ríos (2019, Anartia, 29: 49-53)] = sinchi Henao, 2019 [Ríos (2019, Anartia, 29: 49-53)] ziza (Butler, 1869), Published as part of Espeland, Marianne, Nakahara, Shinichi, Zacca, Thamara, Barbosa, Eduardo P., Huertas, Blanca, Marín, Mario A., Lamas, Gerardo, Benmesbah, Mohamed, Brévignon, Christian, Casagrande, Mirna M., Fåhraeus, Christer, Grishin, Nick, Kawahara, Akito Y., Mielke, Olaf H. H., Miller, Jacqueline Y., Nakamura, Ichiro, Navas, Vanessa, Patrusky, Brooke, Pyrcz, Tomasz W., Richards, Lindsay, Tan, Denise, Tyler, Stephanie, Viloria, Angel, Warren, Andrew D., Xiao, Lei, Freitas, André V. L. & Willmott, Keith R., 2023, Combining target enrichment and Sanger sequencing data to clarify the systematics of the diverse Neotropical butterfly subtribe Euptychiina (Nymphalidae, Satyrinae), pp. 1-73 in Zoological Research 2023 on pages 65-66, DOI: 10.1111/syen.12590, http://zenodo.org/record/7909395

Pareuptychia clade The ‘ Pareuptychia clade’ was proposed first by Murray and Prowell (2005) and corroborated by increasingly comprehensive subsequent studies (Espeland et al., 2019a; Marín et al., 2017; Peña et al., 2006, 2010). The clade contains 11 described genera, Neonympha (2 species), Pareuptychia (9 species), Erichthodes (monotypic), Megeuptychia (3 species), Satyrotaygetis (2 species), Euptychoides (4 species), Taydebis (3 species), Nhambikuara (11 species), Optimandes (2 species), Amiga (2 species), Xenovena gen. n. (monotypic) and an undescribed genus. The ‘ Pareuptychia clade’ is embedded within a larger clade also containing the ‘ Taygetis clade’, ‘ Splendeuptychia clade’ and ‘ Archeuptychia clade’, and we also include the unplaced genus Chloreuptychia in the discussions here (Figures 1, S 1 – S 3). In both FULL trees, Chloreuptychia is sister to the ‘ Pareuptychia clade’, while in both 4GENES trees the genus is sister to the ‘ Archeuptychia clade’. In the backbone tree (Figure S 1) the ‘ Pareuptychia clade’ is sister to the Taygetis clade, and here Chloreuptychia is found to be sister to a clade including the ‘ Taygetis clade’, ‘ Splendeuptychia clade’ and ‘ Archeuptychia clade’. These relationships are not well supported and need to be further investigated. The small genus Amiga is strongly supported as sister group to the remainder of the clade in all datasets. Most generic relationships are well-supported (Figures 9, S 2 and S 3). The clade is divided into two well-supported subclades, the Optimandes subclade (Optimandes, Nhambikuara) and the Pareuptychia subclade (Xenovena gen.n., Pareuptychia, Erichthodes, Neonympha, Euptychoides, Satyrotaygetis, and an undescribed generic-level clade containing some species currently in Erichthodes), consistent with previous molecular studies (Murray & Prowell, 2005; Peña et al., 2010). The placement of Taydebis needs to be further investigated; although it is found as sister to Optimandes + Nhambikuara in all trees, the support for this branch is always low. Since the checklist Lamas (2004), a number of papers have helped revise the generic classification of the ‘ Pareuptychia clade’, with the description of new genera such as Taydebis (Freitas, 2003), Nhambikuara (Freitas, Barbosa, et al., 2018), Amiga (Nakahara, Lamas, et al., 2019) and Optimandes (Willmott et al., 2019), the sorting of species in previously described genera (Andrade-Correa et al., 2019) and descriptions of 11 new species (Benmesbah, 2015; Brévignon, 2005; Freitas et al., 2011; Freitas, Barbosa, et al., 2018; Huertas, 2011; Huertas et al., 2009; Nakahara, Marin, & Neild, 2016; Willmott et al., 2018, 2019). We found strong support for a clade containing the type species of Nhambikuara, N. cerradensis, along with nine other species formerly placed in Splendeuptychia (Lamas, 2004), a relationship partly indicated in Freitas, Barbosa, et al. (2018). Morphological characters also support this as a relatively compact group of species (Huertas, 2014) and we thus transfer the nine former Splendeuptychia species into Nhambikuara (comb.n.). We found strong support for the recently described genus Macrocissia (Andrade-Correa et al., 2019) not being monophyletic, and the two species previously included in this genus are transferred to Satyrotaygetis (Satyrotaygetis iris [C. Felder & R. Felder, 1867]) and Euptychoides (Euptychoides inani [Staudinger, 1886]) in concordance with the phylogeny. The combination of morphological characters used by Andrade-Correa et al. (2019) to support Macrocissia, ‘vestigial recurrent vein into the discal cell’ in the forewing, and ‘valvae with a hook-like distal process’ and a ‘finely serrate cucullus in the male genitalia’, is a combination of characters present in previously described genera such as Satyrotaygetis and Euptychoides, and we thus synonymize Macrocissia syn.n. with Satyrotaygetis. The ‘ Pareuptychia clade’ contains 44 described species, with the genera Pareuptychia and Nhambikuara, with nine and 11 species respectively, being the most diverse. Taxonomic revisions for these two genera are in progress, in addition to work on Taydebis, Euptychoides and Erichthodes. Members of the ‘ Pareuptychia clade’ have a wide distribution, ranging from southern Canada to northern Argentina, and from sea level to almost 2600 m, with the highest diversity in the Amazon basin and the Andes (Marín et al. in preparation). According to Marín et al. (2017), possible synapomorphies (not unique) and/or distinctive characters for the clade include the following: (a) obvious sclerotized cornuti in aedeagus; (b) in the valva, posterior ending of the cucullus acute. Hostplants for members of this clade are mostly bamboos or grasses in the family Poaceae, with records of Cyperaceae in Pareuptychia (Janzen & Hallwachs, 2022) and Neonympha (Hamm et al., 2013), and Marantaceae in Megeuptychia (Janzen & Hallwachs, 2022). Immature stages have been described or illustrated for Amiga, Taydebis, Pareuptychia, Optimandes, Satyrotaygetis, Megeuptychia and Nhambikuara (Corahua-Espinoza, Nakahara, Kabir, et al., 2022; Corahua-Espinoza, Nakahara, Shellman, et al., 2022; Freitas, 2003; Freitas, Barbosa, & Marín, 2016; Janzen & Hallwachs, 2022; Murray, 2001b; Willmott et al., 2019). These are morphologically simple and similar to those of several other species of Neotropical Euptychiina larvae, lacking body scoli, and having short- to medium-sized head horns and caudal filaments, and the pupae are short and smooth., Published as part of Espeland, Marianne, Nakahara, Shinichi, Zacca, Thamara, Barbosa, Eduardo P., Huertas, Blanca, Marín, Mario A., Lamas, Gerardo, Benmesbah, Mohamed, Brévignon, Christian, Casagrande, Mirna M., Fåhraeus, Christer, Grishin, Nick, Kawahara, Akito Y., Mielke, Olaf H. H., Miller, Jacqueline Y., Nakamura, Ichiro, Navas, Vanessa, Patrusky, Brooke, Pyrcz, Tomasz W., Richards, Lindsay, Tan, Denise, Tyler, Stephanie, Viloria, Angel, Warren, Andrew D., Xiao, Lei, Freitas, André V. L. & Willmott, Keith R., 2023, Combining target enrichment and Sanger sequencing data to clarify the systematics of the diverse Neotropical butterfly subtribe Euptychiina (Nymphalidae, Satyrinae), pp. 1-73 in Zoological Research 2023 on page 18, DOI: 10.1111/syen.12590, http://zenodo.org/record/7909395, {"references":["Murray, D. & Prowell, D. P. (2005) Molecular phylogenetics and evolutionary history of the neotropical Satyrine subtribe Euptychiina (Nymphalidae: Satyrinae). Molecular Phylogenetics and Evolution, 34, 67 - 80.","Espeland, M., Breinholt, J., Barbosa, E. P., Casagrande, M., Huertas, B., Lamas, G. et al. (2019 a) Four hundred shades of brown: higher level phylogeny of the problematic Euptychiina (Lepidoptera, Nymphalidae, Satyrinae) based on hybrid enrichment data. Molecular Phylogenetics and Evolution, 131, 116 - 124.","Marin, M. A., Pena, C., Uribe, S. I. & Freitas, A. V. L. (2017) Morphology agrees with molecular data: phylogenetic affinities of Euptychiina butterflies (Nymphalidae: Satyrinae). Systematic Entomology, 42, 768 - 785.","Pena, C., Wahlberg, N., Weingartner, E., Kodandaramaiah, U., Nylin, S., Freitas, A. V. L. et al. (2006) Higher level phylogeny of Satyrinae butterflies (Lepidoptera: Nymphalidae) based on DNA sequence data. Molecular Phylogenetics and Evolution, 40, 29 - 49.","Pena, C., Nylin, S., Freitas, A. V. L. & Wahlberg, N. (2010) Biogeographic history of the butterfly subtribe Euptychiina (Lepidoptera, Nymphalidae, Satyrinae). Zoologica Scripta, 39, 243 - 258.","Lamas, G. (2004) Atlas of Neotropical Lepidoptera. Checklist: Part 4 A Hesperioidea - Papilionoidea. Gainesville: Scientific Publishers / Association of Tropical Lepidoptera, p. 439.","Freitas, A. V. L. (2003) Description of a new genus for \" Euptychia peculiaris \" (Nymphalidae: Satyrinae): immature stages and systematic position. Journal of the Lepidopterists' Society, 57, 100 - 106.","Willmott, K. R., Marin, M. A., Nakahara, S., Pomerantz, T., Lamas, G., Huertas, B. et al. (2019) A revision of the new Andean butterfly genus Optimandes Marin, Nakahara & Willmott, n. gen., with the description of a new species (Nymphalidae: Satyrinae: Euptychiina). Tropical Lepidoptera Research, 29, 29 - 44.","Andrade-Correa, G., Viloria, A´., Henao-Banol, E. R. & Le Crom, J. F. (2019) Generic reassignments of satyrine butterflies from Colombia and Venezuela (Lepidoptera: Nymphalidae). Anartia, 28, 26 - 46.","Benmesbah, M. (2015) Description de deux nouvelles especes de Satyrinae de Guyane franCaise (Lepidoptera, Nymphalidae). Bulletin de la Societe Entomologique de France, 120, 147 - 156.","Brevignon, C. (2005) Description de nouveaux Satyrinae provenant de Guyane franCaise (Lepidoptera, Nymphalidae). Lambillionea, 105, 393 - 404.","Freitas, A., Mielke, O., Moser, A., Silva-Brandao t, K. & Iserhard, C. (2011) A new genus and species of Euptychiina (Lepidoptera: Nymphalidae: Satyrinae) from southern Brazil. Neotropical Entomology, 40, 231 - 237.","Huertas, B. (2011) A new species of satyrid butterfly from Peru (Lepidoptera: Nymphalidae: Satyrinae: Euptychiini). Zootaxa, 2802, 63 - 68.","Huertas, B., Rios-Malaver, C. & Le Crom, J. F. (2009) A new species of Splendeuptychia from the Magdalena Valley in Colombia (Lepidoptera: Nymphalidae: Satyrinae). Zootaxa, 2014, 51 - 58.","Willmott, K. R., Lamas, G., Radford, J. T., Marin, M. A., Nakahara, S., Espeland, M. et al. (2018) A distinctive new species of cloud forest Euptychiina (Lepidoptera: Nymphalidae: Satyrinae) from Ecuador and Peru. Tropical Lepidoptera Research, 28, 39 - 45.","Chazot, N., Willmott, K. R., Lamas, G., Freitas, A. V. L., Piron-Prunier, F., Arias, C. F. et al. (2019) Renewed diversification following Miocene landscape turnover in a Neotropical butterfly radiation. Global Ecology and Biogeography, 28, 1118 - 1132.","Huertas, B. (2014) Systematics of the genus Splendeuptychia (Forster, 1964) and implications of taxonomy in conservation assessments. Chapter 4. In Evaluating the conservation status of Neotropical butterflies and the impact of systematics on threat assessments (PhD thesis). University College London.","Janzen, D. H. & Hallwachs, W. (2022) Area de Conservacion´Guanacaste (ACG), northwestern Costa Rica - caterpillars, pupae, butterflies & moths [WWW document]. Available from: http: // janzen. sas. upenn. edu / caterpillars / database. lasso [Accessed on 1 st January 2022]","Hamm, C. A., Williams, B. L. & Landis, D. A. (2013) Natural history and conservation status of the endangered Mitchell ' s satyr butterfly: synthesis and expansion of our knowledge regarding Neonympha mitchellii mitchellii French 1889. Journal of the Lepidopterists' Society, 67, 15 - 28.","Murray, D. L. (2001 b) Systematics of euptychiine butterflies (Nymphalidae: Satyrinae: Euptychiina) based on larval morphology and DNA sequence data and the evolution of life history traits (PhD thesis). Louisiana State University. 367 pp."]}

Koutalina Viloria & Murienne, 2021 pamela (Hayward, 1957) [Benmesbah et al. (2021, Anartia, 31: 7-62)], Published as part of Espeland, Marianne, Nakahara, Shinichi, Zacca, Thamara, Barbosa, Eduardo P., Huertas, Blanca, Marín, Mario A., Lamas, Gerardo, Benmesbah, Mohamed, Brévignon, Christian, Casagrande, Mirna M., Fåhraeus, Christer, Grishin, Nick, Kawahara, Akito Y., Mielke, Olaf H. H., Miller, Jacqueline Y., Nakamura, Ichiro, Navas, Vanessa, Patrusky, Brooke, Pyrcz, Tomasz W., Richards, Lindsay, Tan, Denise, Tyler, Stephanie, Viloria, Angel, Warren, Andrew D., Xiao, Lei, Freitas, André V. L. & Willmott, Keith R., 2023, Combining target enrichment and Sanger sequencing data to clarify the systematics of the diverse Neotropical butterfly subtribe Euptychiina (Nymphalidae, Satyrinae), pp. 1-73 in Zoological Research 2023 on page 56, DOI: 10.1111/syen.12590, http://zenodo.org/record/7909395

Graphita Nakahara, Marín & Barbosa, 2016 griphe (C. Felder & R. Felder, 1867) [Nakahara et al. (2016, Neotropical Entomology, 45: 675-691)] = vesta (Butler, 1867) [Nakahara et al. (2016, Neotropical Entomology, 45: 675-691)] = ucumariensis (Andrade, 1991) [Nakahara et al. (2016, Neotropical Entomology, 45: 675-691)], Published as part of Espeland, Marianne, Nakahara, Shinichi, Zacca, Thamara, Barbosa, Eduardo P., Huertas, Blanca, Marín, Mario A., Lamas, Gerardo, Benmesbah, Mohamed, Brévignon, Christian, Casagrande, Mirna M., Fåhraeus, Christer, Grishin, Nick, Kawahara, Akito Y., Mielke, Olaf H. H., Miller, Jacqueline Y., Nakamura, Ichiro, Navas, Vanessa, Patrusky, Brooke, Pyrcz, Tomasz W., Richards, Lindsay, Tan, Denise, Tyler, Stephanie, Viloria, Angel, Warren, Andrew D., Xiao, Lei, Freitas, André V. L. & Willmott, Keith R., 2023, Combining target enrichment and Sanger sequencing data to clarify the systematics of the diverse Neotropical butterfly subtribe Euptychiina (Nymphalidae, Satyrinae), pp. 1-73 in Zoological Research 2023 on page 56, DOI: 10.1111/syen.12590, http://zenodo.org/record/7909395

Deltaya Willmott, Nakahara & Espeland, genus novum. Type species — Papilio ocypete Fabricius, [1777], by pre- sent designation. Zoobank registration: https://zoobank.org/Nomenclatural Acts/C5441C63-9631-4E9D-A37F-6ED27676D185 Systematic placement and diagnosis. Deltaya gen.n. is a member of the ‘ Splendeuptychia clade’ (Figure 10), and three of its four ‘core’ described species, Deltaya ocypete comb.n, Deltaya louisammour comb.n and Deltaya opima comb.n. (Figures 33 and 34), form a clade with low support (FULL dataset SH-aLRT = 67.9, UFB = 53). Deltaya pallema comb.n. is closely related to D. ocypete and is also considered a ‘core’ species (Benmesbah et al., 2018). Two species are placed with some support as forming a grade sister to this clade (SHaLRT = 85.4, UFB = 83) and are included here within the genus (Deltaya andrei comb.n. and Deltaya probata comb.n, see Discussion below). Within the ‘ Splendeuptychia clade’, Deltaya gen.n. is a member of the same clade as Modica gen.n., Paryphthimoides, Colombeia, Scriptor, and Malaveria, with it being placed as sister to Scriptor (SHaLRT = 98.3, UFB = 61), but none of the nodes connecting these genera have strong support. Deltaya gen.n. lacks obvious morphological synapomorphies, but the following are somewhat distinctive characters within Euptychiina (shared variously with other genera) on the ventral wings (Figures 33 and 34): relatively broad dark transverse discal bands; the presence of only five relatively large postdiscal VHW ocelli, with each ocellus having two pupils, which are small dots (in cells Cu 2 -Cu 1, M 2 - M 1) or elongate and large (in cells Cu 1 - M 3, M 3 - M 2, M 1 -Rs), and the postdiscal ocelli on both wings lying within a broad darker band (umbra). Overall, the genus is best distinguished from phenotypically similar genera by the pale pupils of the HW ocellus in cell Cu 2 -Cu 1 not being visible on the dorsal surface, by the VHW postdiscal ocelli in cells Cu 1 -M 3 and M 3 -M 2 being of similar size, round (not elongate) and each containing two enlarged, elongated silver pupils (when the ocelli are large enough for the pupils to be visible), and by the marginal line widening in the VHW tornus. This last character also occurs in Scriptor, some Paryphthimoides, and some other Euptychiina (e.g. Vanima labe, Vanima palladia), but is otherwise a relatively uncommon character. Characters that differ among the genera within the clade in which Deltaya gen.n. is placed are summarized in Table 1. The genitalia of both sexes are described below and there are no obvious synapomorphies for the genus as a whole. However, ‘core’ Deltaya gen.n. (Figure 35) share several distinctive characters, including: (a) the aedeagus has two relatively long and broad rectangular patches of cornuti (smaller or no patches in other species). (b) in the female, the anterior half of the 8th tergite is weakly sclerotized and the intersegmental membrane between the 7th and 8th segments is pleated and expandable; (c) the ventral portion of the intersegmental membrane between the 7th and 8th segments bears a sclerotized plate similar to the 7th sternite; (d) a sclerotized rectangular lamella antevaginalis extending horizontally and fused with the lateral plate of the 8th abdominal segment is present (as noted by Nakahara, Kleckner, et al., 2020). Etymology. The generic name is derived from the name of the fourth letter of the Greek alphabet, delta, whose triangular upper-case symbol is the source of the word used in multiple languages to describe the broadening of a river at its mouth. The name is treated as a feminine noun in the nominative singular, and refers to the broadening VHW marginal line at the tornus that distinguishes Deltaya species from a number of other similar species. Description (Figures 33 – 35). Some notable characters include: eyes setose; pterothoracic legs dorsally slightly darker, tibia with two principal longitudinal rows of spines ventrally, pair of spurs of similar length at distal end of tibia, first tarsomere with three principal longitudinal rows of spines ventrally, remaining tarsomeres with four principal longitudinal rows of spines ventrally. Medium-sized Euptychiina (FW length typically 19 – 25 mm), FW triangular and rather rounded at apex, HW rounded. No strong sexual dimorphism: Dorsal wings dark brown to blue-grey, pale pupils of ocellus in Cu 2 -Cu 1 not visible on DHW, no androconial scales present. Ventral wings blue-grey to brownish grey; relatively broad, dark brown to reddish brown discal and postdiscal lines traversing both wings; VFW with three postdiscal ocelli in cells Cu 1 -M 3, M 3 -M 2, M 2 -M 1, anterior ocellus more clearly marked than remainder, lying within a broad dark brown band (umbra); VHW similar to VFW but with five postdiscal ocelli between veins Cu 2 and Rs, those in Cu 2 -Cu 1 and M 2 -M 1 typically slightly larger, black-centred with two silver dots in each ocellus as pupils, ocelli in M 1 -Rs similar but much smaller, and those in Cu 1 -M 2 with dark brown centres and elongate silver pupils; marginal line thin and even throughout (except rather broad throughout in D. probata comb.n.), thickening noticeably at tornus. Male eighth abdominal tergite reduced dorsally, leaving a sclerotized strip along anterior edge and no or an isolated weakly sclerotized patch in posterior portion. Male genitalia with uncus longer than tegumen, brachia pointing slightly dorsally of uncus and about two-thirds its length; valvae elongate with dorsal edge straight or (‘core’ Deltaya gen.n.) with projection near distal tip covered with tiny spines; aedeagus lacking cornuti but with tiny spines scattered dorsally in D. probata comb.n. and D. andrei comb.n., and with cornuti in ‘core’ Deltaya gen.n. forming two relatively broad and long rectangular patches of tiny spines; intersegmental membrane between eighth segment and genitalic capsule in D. andrei comb.n. forms a ventro-lateral, eversible ‘pocket’ containing dense, long, black scales. Female genitalia has eighth tergite reduced to a posterior sclerotized patch about one- to two-thirds width of segment, eighth segment with large irregular lateral sclerotized plate extending broadening dorsally and with indentation at dorsal edge, antrum unsclerotized, ductus bursae unsclerotized, corpus bursae small, oval and with two narrow sub-parallel signa. ‘Core’ Deltaya gen. n. have additional characters described above under Diagnosis. Distribution and natural history (Figure 36). Deltaya gen.n. contains six described species and probably several undescribed species, which occur in rainforest from sea level to 1400 m and are confined to South America east of the Andes. The genus reaches its peak diversity in the central and western Amazon, where both sexes are typically uncommon in the understory of both disturbed and undisturbed forest, except for D. ocypete comb.n., which may also be locally common in secondary habitats, including in the drier interandean valleys and extra-Amazonian regions from Bolivia across to south-eastern Brazil. Deltaya gen.n. species have also been recorded in fruit-baited traps (Benmesbah et al., 2018; Oliveira et al., 2021; Zacca, Casagrande, et al., 2017). The immature stages have not been described for any species to date, and while there are records of Cyperaceae and Poaceae as hostplants of D. ocypete comb.n. (Singer & Ehrich, 1993), these require confirmation given prior confusion over the identification of this species. Discussion. Benmesbah et al. (2018) discussed in detail the taxonomic history of the type species of this genus, Papilio ocypete, and designated a specimen with a DNA barcode as the neotype. This species and three other described species, D. opima comb.n., D. louisammour comb.n. and D. pallema comb.n., form a clade based on DNA sequences (‘core’ Deltaya gen. n. ), and share several morphological synapomorphies. All these species were previously placed in Magneuptychia by Lamas (2004), but, for the same reasons as discussed under Modica gen.n., they cannot reasonably be accommodated in any described genus, except perhaps Scriptor. Nevertheless, monophyly with Scriptor is only weakly supported in our results, and we thus believe that description of a new genus is the best solution. As mentioned above under Systematic Placement and Diagnosis, we also provisionally include two species in Deltaya that are weakly supported based on molecular data as members of the same clade as ‘core’ Deltaya gen.n., namely D. probata comb.n. (Figure 34d) and D. andrei comb.n. (Figure 34c). Although both species share some wing pattern and genitalic similarities with ‘core’ Deltaya gen. n. , none of these are convincing synapomorphies for Deltaya gen.n. Deltaya andrei comb.n. has a very distinctive autapomorphy, namely a pocket of dense black scales adjacent to the valvae in the male genitalia, while the wing pattern of D. probata comb.n. is rather different from the remaining Deltaya species, with a VHW marginal line that is thickened throughout. Only COI sequences are available for D. probata comb.n., and COI + RPS5 for D. andrei comb.n., and more complete molecular data for both species and other members of the ‘ Splendeuptychia clade’ are therefore needed to confirm the generic classification of D. andrei and D. probata. Deltaya Willmott, Nakahara & Espeland, gen.n. andrei (Zacca, Casagrande & Mielke, 2017), comb.n., was Magneuptychia [Zacca et al. (2017, Zootaxa, 4231(3): 442-450)] louisammour (Benmesbah & Zacca, 2018), comb.n., was Magneuptychia [Benmesbah et al. (2018, Zootaxa, 4425(1): 115-145)] ocypete (Fabricius, [1777]), comb.n., was Magneuptychia = sabina (C. Felder & R. Felder, 1867), comb.n., was Magneuptychia = olivacea (Aurivillius, 1929), comb.n., was Magneuptychia opima (Weymer, 1911), comb.n., was Magneuptychia pallema (Schaus, 1902), comb.n., was Magneuptychia probata (Weymer, 1911), comb.n., was Magneuptychia = aliciae (Hayward, 1957), comb.n., was Magneuptychia, Published as part of Espeland, Marianne, Nakahara, Shinichi, Zacca, Thamara, Barbosa, Eduardo P., Huertas, Blanca, Marín, Mario A., Lamas, Gerardo, Benmesbah, Mohamed, Brévignon, Christian, Casagrande, Mirna M., Fåhraeus, Christer, Grishin, Nick, Kawahara, Akito Y., Mielke, Olaf H. H., Miller, Jacqueline Y., Nakamura, Ichiro, Navas, Vanessa, Patrusky, Brooke, Pyrcz, Tomasz W., Richards, Lindsay, Tan, Denise, Tyler, Stephanie, Viloria, Angel, Warren, Andrew D., Xiao, Lei, Freitas, André V. L. & Willmott, Keith R., 2023, Combining target enrichment and Sanger sequencing data to clarify the systematics of the diverse Neotropical butterfly subtribe Euptychiina (Nymphalidae, Satyrinae), pp. 1-73 in Zoological Research 2023 on pages 38-67, DOI: 10.1111/syen.12590, http://zenodo.org/record/7909395, {"references":["Benmesbah, M., Zacca, T., Casagrande, M. M., Mielke, O. H. H., Lamas, G. & Willmott, K. R. (2018) Taxonomic notes on Papilio ocypete Fabricius, 1776 and Papilio helle Cramer, 1779 with description of two new similar species from South America (Lepidoptera: Nymphalidae: Satyrinae). Zootaxa, 4425, 115 - 145.","Oliveira, I. F., Baccaro, F. B., Werneck, F. P., Zacca, T. & Haugaasen, T. (2021) Marked differences in butterfly assemblage composition between forest types in Central Amazonia, Brazil. Forests, 12, 942.","Singer, M. & Ehrich, P. (1993) Host specialization of satyrine butterflies, and their responses to habitat fragmentation in Trinidad. Journal of Research on the Lepidoptera, 30, 248 - 256.","Lamas, G. (2004) Atlas of Neotropical Lepidoptera. Checklist: Part 4 A Hesperioidea - Papilionoidea. Gainesville: Scientific Publishers / Association of Tropical Lepidoptera, p. 439.","Zacca, T., Casagrande, M. M., Mielke, O. H. H., Huertas, B., Neild, A. F. E. & Benmesbah, M. (2017) Description of a new species of Euptychiina (Lepidoptera: Nymphalidae: Satyrinae) from South America. Zootaxa, 4231, 442 - 450.","Aurivillius, P. O. C. (1929) Wissenschaftliche Ergebnisse der schwedischen Entomologischen Reisen des Herrn Dr. A. Roman in Amazonas 1914 - 1915 und 1923 - 1924. 13. Rhopalocera. Entomologisk Tidskrift, 50, 153 - 168.","Weymer, G. (1911) 4. Familie: Satyridae. In: Seitz, A. (Ed.) Die GrossSchmetterlinge der Erde. Stuttgart: A. Kernen, pp. 173 - 280."]}

Erichthodes Forster, 1964 antonina (C. Felder & R. Felder, 1867) = erichtho (Butler, 1867), Published as part of Espeland, Marianne, Nakahara, Shinichi, Zacca, Thamara, Barbosa, Eduardo P., Huertas, Blanca, Marín, Mario A., Lamas, Gerardo, Benmesbah, Mohamed, Brévignon, Christian, Casagrande, Mirna M., Fåhraeus, Christer, Grishin, Nick, Kawahara, Akito Y., Mielke, Olaf H. H., Miller, Jacqueline Y., Nakamura, Ichiro, Navas, Vanessa, Patrusky, Brooke, Pyrcz, Tomasz W., Richards, Lindsay, Tan, Denise, Tyler, Stephanie, Viloria, Angel, Warren, Andrew D., Xiao, Lei, Freitas, André V. L. & Willmott, Keith R., 2023, Combining target enrichment and Sanger sequencing data to clarify the systematics of the diverse Neotropical butterfly subtribe Euptychiina (Nymphalidae, Satyrinae), pp. 1-73 in Zoological Research 2023 on page 64, DOI: 10.1111/syen.12590, http://zenodo.org/record/7909395