340 results on '"Richards, Lindsay"'
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2. Erosion-inhibiting potential of the stannous fluoride-enriched CPP-ACP complex in vitro
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Al Saady, Deena, Hall, Colin, Edwards, Suzanne, Reynolds, Eric C., Richards, Lindsay C., and Ranjitkar, Sarbin
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- 2023
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3. Abortion education: What are future physicians learning in medical school?
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Heger, Julie A., Young, BreAnne J., Richards, Lindsay R., Carrasquillo, Olveen, and Kenya, Sonjia
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- 2024
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4. Subjective socioeconomic status and self-rated health in the English Longitudinal Study of Aging: A fixed-effects analysis
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Coustaury, Camille, Jeannot, Elias, Moreau, Adele, Nietge, Clotilde, Maharani, Asri, Richards, Lindsay, and Präg, Patrick
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- 2023
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5. Subjective social status and allostatic load among older people in England: A longitudinal analysis
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Richards, Lindsay, Maharani, Asri, and Präg, Patrick
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- 2023
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6. Can Community Health Workers in Miami Disrupt Disparities among Black People Living with HIV: A Qualitative Analysis
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Kenya, Sonjia, primary, Young, BreAnne, additional, Richards, Lindsay, additional, Casanova, Felicia, additional, Rodriguez, Allan, additional, Blackmon, Jakisha, additional, Carrasquillo, Olveen, additional, Pan, Yue, additional, and Jones-Weiss, Deborah, additional
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- 2024
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7. Political Values and Political Participation
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Heath, Anthony F., primary, Richards, Lindsay, additional, and Jungblut, Julia, additional
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- 2022
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8. Subjective social status and trajectories of frailty: findings from the English Longitudinal Study of Ageing
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Maharani, Asri, primary, Richards, Lindsay, additional, and Präg, Patrick, additional
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- 2024
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9. Does downward social mobility make people more hostile towards immigrants?
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Paskov, Marii, Präg, Patrick, and Richards, Lindsay
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- 2021
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10. Intergenerational social mobility and allostatic load in Great Britain
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Präg, Patrick and Richards, Lindsay
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- 2019
11. For whom money matters less : patterns of connectedness and psychosocial resilience
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Richards, Lindsay Anne
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302 ,Money-happiness ,Social connectedness ,Psycho-social resilience - Abstract
The positive association between income and subjective well-being (SWB) is undisputed; there remains scope, however, to expand our understanding of the explanatory mechanisms at work. The theoretical framing is formed from economics and psychology which have been the traditional homes of happiness research. However, the stance taken here is sociological in its attention to social networks and social status. I also emphasise psychological benefits as an explanatory mechanism for the money-happiness relationship. Following Layard (1981) and Easterlin (2001), it is posited that above the level at which basic needs are met, higher SWB results from the higher rank in society that money brings. I argue that rank and status inform how individuals feel about themselves (self-esteem, self-worth) and their environment (perceived control) and that it is these factors that bring about SWB. Furthermore, social connectedness is an alternative source of these benefits and it is thus hypothesised that connectedness will intervene in the money-happiness relationship. Secondary or “weak” ties are expected to have an additional and separable effect to close ties alone. I use the term resilience as a framing concept as it allows the stressor (financial situation) and outcome (SWB) to be discussed in a single term. The thesis has three empirical aims. The first is to determine whether connectedness influences the money happiness relationship, where ‘money’ refers to household income, perceived financial situation and being worse off than the previous year. Secondly, I aim to separate the effect of connectedness from the effect of personal characteristics by observing outcomes before and after a change in connectedness. Third, I aim to unravel the potentially paradoxical role of networks for those on low incomes as both a resilience resource and therefore greater happiness, and as a source of wider social comparison and therefore greater unhappiness. I use data from seven waves of the British Household Panel Survey. A latent class analysis establishes a measurement schema of connectedness based on strong and weak ties. Growth curve models are used to measure the effect of money on SWB and differential effects by connectedness are demonstrated with interaction terms. Resilience before and after network changes are explored using multiple group linear regression at two time points, and neighbourhood social comparison is examined in multilevel models. The findings are that income has no bearing on the SWB of the socially-integrated (those with both strong and weak ties) while the isolated have a lot to gain. The SWB of the integrated does suffer in difficult financial circumstances as subjectively reported but less so than the isolated or those with only strong ties. Further, when individuals expand their network it is accompanied by a decrease in the importance of income for SWB. These patterns can in part be explained by the fact that the SWB of the well-connected is less influenced by their position relative to those living around them, at least where the income gap is not too large. Therefore, the assumption of happiness as a zero-sum game is mistaken; social comparison is not inevitable and SWB can be maintained through social integration providing the level of inequality is not too high.
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- 2015
12. Biogeographical characteristics of Schistosoma mansoni endemic areas in Ethiopia: a systematic review and meta analysis
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Ponpetch, Keerati, Erko, Berhanu, Bekana, Teshome, Richards, Lindsay, and Liang, Song
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- 2021
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13. Leave and Remain voters’ knowledge of the EU after the referendum of 2016
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Carl, Noah, Richards, Lindsay, and Heath, Anthony
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- 2019
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14. Abortion education: What are future physicians learning in medical school?
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Heger, Julie A., primary, Young, BreAnne J., additional, Richards, Lindsay R., additional, Carrasquillo, Olveen, additional, and Kenya, Sonjia, additional
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- 2023
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15. Generational Differences in Local Identities, Participation in Social Movements, and Migration Intention Among Hong Kong People
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Kan, Man-Yee, primary, Loa, See Pok, additional, and Richards, Lindsay, additional
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- 2023
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16. How Divided Is Britain? Symbolic Boundaries and Social Cohesion in Post-Brexit Britain
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Richards, Lindsay, primary and Heath, Anthony, additional
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- 2023
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17. Combining target enrichment and Sanger sequencing data to clarify the systematics of the diverse Neotropical butterfly subtribe Euptychiina (Nymphalidae, Satyrinae)
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Espeland, Marianne, primary, Nakahara, Shinichi, additional, Zacca, Thamara, additional, Barbosa, Eduardo P., additional, Huertas, Blanca, additional, Marín, Mario A., additional, Lamas, Gerardo, additional, Benmesbah, Mohamed, additional, Brévignon, Christian, additional, Casagrande, Mirna M., additional, Fåhraeus, Christer, additional, Grishin, Nick, additional, Kawahara, Akito Y., additional, Mielke, Olaf H. H., additional, Miller, Jacqueline Y., additional, Nakamura, Ichiro, additional, Navas, Vanessa, additional, Patrusky, Brooke, additional, Pyrcz, Tomasz W., additional, Richards, Lindsay, additional, Tan, Denise, additional, Tyler, Stephanie, additional, Viloria, Ángel, additional, Warren, Andrew D., additional, Xiao, Lei, additional, Freitas, André V. L., additional, and Willmott, Keith R., additional
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- 2023
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18. The Oral Health of a Group of 19th Century South Australian Settlers in Relation to Their General Health and Compared with That of Contemporaneous Samples
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Gurr, Angela, primary, Henneberg, Maciej, additional, Kumaratilake, Jaliya, additional, Lerche, Derek, additional, Richards, Lindsay, additional, and Brook, Alan Henry, additional
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- 2023
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19. The use of a psychological testing instrument as an indicator of dissatisfaction with aesthetic dental treatment – a preliminary study
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Dudley, James, Richards, Lindsay, and Mahmud, Melati
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- 2020
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20. Fuzzy Frontiers? Testing the Fluidity of National, Partisan and Brexit Identities in the Aftermath of the 2016 Referendum.
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Kenny, John, Heath, Anthony, and Richards, Lindsay
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NATIONALISM ,PARTISANSHIP ,BREXIT Referendum, 2016 - Abstract
British and English national identities have long been considered to have porous boundaries whereby English individuals consider the terms more or less interchangeable. However, there is no empirical evidence to demonstrate whether primary feelings of either Britishness or Englishness are highly fluid within-individuals or whether individuals are consistent in their perceptions of their British or English identity. This is especially relevant in the post-Brexit referendum context where national identity is highly correlated with Brexit attitudes. Using panel data, we demonstrate that there is a notable degree of fluidity between identifying as British or English. This is higher than the fluidity between other national identities in the UK as well as more fluid than moving between any partisan or EU referendum identities. Remainers are more fluid than Leavers in their Englishness, whereas they are similar in the fluidity of their Britishness. [ABSTRACT FROM AUTHOR]
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- 2023
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21. The Fight against Disease
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Heath, Anthony F., primary, Garratt, Elisabeth, additional, Kashyap, Ridhi, additional, Li, Yaojun, additional, and Richards, Lindsay, additional
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- 2018
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22. The Fight against Squalor
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Heath, Anthony F., primary, Garratt, Elisabeth, additional, Kashyap, Ridhi, additional, Li, Yaojun, additional, and Richards, Lindsay, additional
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- 2018
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23. Progress in Tackling Beveridge’s Five Giants
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Heath, Anthony F., primary, Garratt, Elisabeth, additional, Kashyap, Ridhi, additional, Li, Yaojun, additional, and Richards, Lindsay, additional
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- 2018
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24. The Fight against Idleness
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Heath, Anthony F., primary, Garratt, Elisabeth, additional, Kashyap, Ridhi, additional, Li, Yaojun, additional, and Richards, Lindsay, additional
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- 2018
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25. The Challenge of Social Corrosion
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Heath, Anthony F., primary, Garratt, Elisabeth, additional, Kashyap, Ridhi, additional, Li, Yaojun, additional, and Richards, Lindsay, additional
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- 2018
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26. The Fight against Want
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Heath, Anthony F., primary, Garratt, Elisabeth, additional, Kashyap, Ridhi, additional, Li, Yaojun, additional, and Richards, Lindsay, additional
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- 2018
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27. Beveridge’s Five Giants and Other Challenges to Social Progress
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Heath, Anthony F., primary, Garratt, Elisabeth, additional, Kashyap, Ridhi, additional, Li, Yaojun, additional, and Richards, Lindsay, additional
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- 2018
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28. Social Progress in Britain
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Heath, Anthony F., primary, Garratt, Elizabeth, additional, Kashyap, Ridhi, additional, Li, Yaojun, additional, and Richards, Lindsay, additional
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- 2018
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29. The Challenge of Inequality of Opportunity
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Heath, Anthony F., primary, Garratt, Elisabeth, additional, Kashyap, Ridhi, additional, Li, Yaojun, additional, and Richards, Lindsay, additional
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- 2018
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30. Young People in Transition: The National Identity of Minority Youth
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Heath, Anthony, primary, Jacob, Konstanze, additional, and Richards, Lindsay, additional
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- 2018
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31. Social class, employment status and inequality in psychological well-being in the UK: Cross-sectional and fixed effects analyses over two decades
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Richards, Lindsay and Paskov, Marii
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- 2016
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32. A descriptive analysis of the Canadian prehospital and transport transfusion (CAN-PATT) network
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Greene, Adam, primary, Trojanowski, Jan, additional, Shih, Andrew W., additional, Evans, Rob, additional, Chang, Eddie, additional, Nahirniak, Susan, additional, Pearson, Dallas, additional, Prokopchuk-Gauk, Oksana, additional, Martin, Doug, additional, Musuka, Charles, additional, Seidl, Cindy, additional, Peddle, Michael, additional, Lin, Yulia, additional, Smith, Justin A., additional, MacDonald, Scott, additional, Richards, Lindsay, additional, Farrell, Michael, additional, and Nolan, Brodie, additional
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- 2023
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33. Understanding the impact of a social support program in Immokalee, FL, during the COVID-19 pandemic
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Richards, Lindsay, primary, Wang, Leping, additional, Jeanmarie, Joashilia, additional, Shafazand, Shirin, additional, Palazuelos, Daniel, additional, and Monacello, Vitina, additional
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- 2023
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34. Effect of remaining tooth structure on the fracture resistance of endodontically-treated maxillary premolars: An in vitro study
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Ibrahim, Amal Mamdouh B.R., Richards, Lindsay C., and Berekally, Thomas L.
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- 2016
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35. For Whom Money Matters Less : Social Connectedness as a Resilience Resource in the UK
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Richards, Lindsay
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- 2016
36. Explaining Corruption in the Developed World: The Potential of Sociological Approaches
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Heath, Anthony F., Richards, Lindsay, and de Graaf, Nan Dirk
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- 2016
37. Modica Zacca, Casagrande & Willmott 2023
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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., and Willmott, Keith R.
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Lepidoptera ,Insecta ,Arthropoda ,Animalia ,Nymphalidae ,Modica ,Biodiversity ,Taxonomy - Abstract
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."]}
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- 2023
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38. Occulta Nakahara & Willmott 2023
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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., and Willmott, Keith R.
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Lepidoptera ,Insecta ,Occulta ,Arthropoda ,Animalia ,Nymphalidae ,Biodiversity ,Taxonomy - Abstract
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."]}
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39. Cissia Doubleday 1848
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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., and Willmott, Keith R.
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Lepidoptera ,Insecta ,Arthropoda ,Animalia ,Nymphalidae ,Biodiversity ,Cissia ,Taxonomy - Abstract
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
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40. Argentaria Huertas & Willmott 2023
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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., and Willmott, Keith R.
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Lepidoptera ,Insecta ,Arthropoda ,Animalia ,Nymphalidae ,Argentaria ,Biodiversity ,Taxonomy - Abstract
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
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41. Amiga Nakahara, Willmott & Espeland 2019
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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., and Willmott, Keith R.
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Lepidoptera ,Insecta ,Arthropoda ,Animalia ,Nymphalidae ,Biodiversity ,Amiga ,Taxonomy - Abstract
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
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42. Orotaygetis Nakahara & Zacca 2018
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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., and Willmott, Keith R.
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Lepidoptera ,Insecta ,Arthropoda ,Orotaygetis ,Animalia ,Nymphalidae ,Biodiversity ,Taxonomy - Abstract
Orotaygetis Nakahara & Zacca, 2018 surui Nakahara, Zacca & Lamas, 2018 [Nakahara et al. (2018, Insecta Mundi, 0639: 1-38)]
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43. Taydebis Freitas 2003
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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., and Willmott, Keith R.
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Lepidoptera ,Insecta ,Arthropoda ,Taydebis ,Animalia ,Nymphalidae ,Biodiversity ,Taxonomy - Abstract
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
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44. Atlanteuptychia Freitas, Barbosa & Mielke 2013
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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., and Willmott, Keith R.
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Lepidoptera ,Insecta ,Arthropoda ,Animalia ,Nymphalidae ,Biodiversity ,Atlanteuptychia ,Taxonomy - Abstract
Atlanteuptychia Freitas, Barbosa & Mielke, 2013 ernestina (Weymer, 1911) [Freitas et al. (2013, Zoologia, 30: 661-668)]
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45. Paramacera Butler 1868
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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., and Willmott, Keith R.
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Lepidoptera ,Insecta ,Arthropoda ,Animalia ,Nymphalidae ,Biodiversity ,Paramacera ,Taxonomy - Abstract
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
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46. Pseudeuptychia Forster 1964
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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., and Willmott, Keith R.
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Lepidoptera ,Insecta ,Arthropoda ,Animalia ,Nymphalidae ,Biodiversity ,Pseudeuptychia ,Taxonomy - Abstract
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
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47. Koutalina Viloria & Murienne 2021
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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., and Willmott, Keith R.
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Lepidoptera ,Insecta ,Koutalina ,Arthropoda ,Animalia ,Nymphalidae ,Biodiversity ,Taxonomy - Abstract
Koutalina Viloria & Murienne, 2021 pamela (Hayward, 1957) [Benmesbah et al. (2021, Anartia, 31: 7-62)]
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48. Trico tricolor subsp. tricolor
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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., and Willmott, Keith R.
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Lepidoptera ,Insecta ,Arthropoda ,Animalia ,Nymphalidae ,Biodiversity ,Trico ,Trico tricolor ,Trico tricolor tricolor (hewitson, 1850) ,Taxonomy - Abstract
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."]}
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49. Optimandes Marin, Nakahara & Willmott 2019
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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., and Willmott, Keith R.
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Lepidoptera ,Optimandes ,Insecta ,Arthropoda ,Animalia ,Nymphalidae ,Biodiversity ,Taxonomy - Abstract
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
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50. Emeryus probata Zacca, Casagrande & Mielke 2020
- Author
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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., and Willmott, Keith R.
- Subjects
Lepidoptera ,Insecta ,Arthropoda ,Animalia ,Nymphalidae ,Biodiversity ,Emeryus ,Taxonomy - Abstract
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)]
- Published
- 2023
- Full Text
- View/download PDF
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