Startseite Lebenswissenschaften New records of Clusiidae (Diptera: Schizophora), including three species new to North America
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New records of Clusiidae (Diptera: Schizophora), including three species new to North America

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Veröffentlicht/Copyright: 28. Juni 2024

Abstract

New geographic records are presented for species in all three subfamilies of Clusiidae (Diptera: Schizophora) from Nearctic, Palearctic, and Neotropical localities. Three Neotropical species are recorded in the United States for the first time: Sobarocephala lucibilis Lonsdale & Marshall, Sobarocephala oculata Lonsdale & Marshall, and Heteromeringia fumipennis Melander & Argo. Emendations to the key to Nearctic Sobarocephala are provided to accommodate the newly recorded species, and figures and diagnoses of both are given. The boundaries of Sobarocephala affinis (Johnson) and Sobarocephala muesebecki Sabrosky & Steyskal are discussed.

Resumen

Se presentan nuevos registros geográficos de especies en las tres subfamilias de Clusiidae (Diptera: Schizophora), basados en localidades del Neárctico, Paleártico y Neotrópico. Tres especies, previamente sólo conocidas del Neotrópico, se reportan por primera vez para los Estados Unidos: Sobarocephala lucibilis Lonsdale & Marshall, Sobarocephala oculata Lonsdale & Marshall, y Heteromeringia fumipennis Melander & Argo. Se proporcionan correcciones a la clave de especies de Sobarocephala del Neárctico para incluir las dos especies adicionales, incluyendo imágenes y caracteres diagnósticos. Se discuten los límites entre las especies Sobarocephala affinis (Johnson) y Sobarocephala muesebecki Sabrosky & Steyskal.

1 Introduction

The diversity, distribution and phylogenetics of the family Clusiidae (Diptera) have been documented extensively as of late, particularly in a series of studies from Lonsdale and Marshall (see citations in Lonsdale [2017]), with the fauna of the Palearctic, Nearctic, and Neotropical regions receiving the most attention. Despite this, new data on the family still accumulate with regularity, and it is apparent that there are still numerous undescribed species in all three subfamilies. Most undescribed taxa are Old World representatives of the diverse clusiodine genera Czernyola Bezzi, Hendelia Czerny, and Heteromeringia Czerny, but also the clusiine genus Tetrameringia McAlpine, and there are likely many additional species of Neotropical Sobaocephala Czerny (Sobarocephalinae) left undescribed, despite their recent revision.

The present work is not intended to describe new taxa but will instead restrict itself to the recording of new geographic records of known species at the country, province, and state levels. Several of these records represent the first Nearctic records of three otherwise Neotropical species: Sobarocephala lucibilis Lonsdale & Marshall and Sobarocephala oculata Lonsdale & Marshall were collected in Miami, Florida, at Montgomery Botanical Garden, and Heteromeringia fumipennis Melander & Argo was found in Baton Rouge, Louisiana.

In an attempt to frame these disparate global records from across the Nearctic, Palearctic and Neotropical regions, the results of this study will be divided into three sections. In the first section, the Clusiidae of Florida are reviewed and Lonsdale and Marshall’s (2007a) key to Nearctic Sobarocephala is emended. In the second section, the remaining new geographic records are presented within each subfamily. In the last section, the species limits of the Nearctic species Sobarocephala affinis (Johnson) and Sobarocephala muesebecki Sabrosky & Steyskal are discussed.

2 Materials and methods

All examined specimens were pinned museum specimens. Specimen data were digitized in the Canadian National Collection of Insects, Arachnids & Nematodes, Ottawa, Ontario (CNC) specimen database (https://www.cnc.agr.gc.ca/taxonomy/TaxonMain.php). When necessary, male genitalia were dissected using hot lactic acid followed by washing in ethanol; genitalia were stored in glycerin in microvials pinned to the same pin as the specimen. Label data were partially translated verbatim, with some data ordered and expanded during databasing (abbreviations expanded, latitude and longitude added, etc.). Classification of the family follows Lonsdale (2017). Limits of biogeographic regions follow Thompson (1999).

Depository acronyms used below are CNC (Canadian National Collection of Insects, Arachnids & Nematodes, Ottawa, Ontario), CUAC (Clemson University, Clemson, South Carolina), LSAM (Louisiana State Arthropod Museum, Baton Rouge, Louisiana), and MEMU (Mississippi State University, Mississippi).

3 Results

3.1 The Clusiidae of Florida

The Nearctic Sobarocephala (Sobarocephalinae) were last revised by Lonsdale and Marshall (2007a). Sobarocephala dreisbachi Sabrosky and Steyskal was later added to the Florida list by Halbert (2003) following detection by G. Steck (Florida Department of Agriculture and Consumer Services, Gainesville, Florida). Herein, two Neotropical Sobarocephala are recorded in the Nearctic region for the first time: S. lucibilis and S. oculata. Collection data and diagnoses of the two newly added species are as follows:

  1. S. lucibilis Lonsdale & Marshall (Figure 1)

    New biogeographic region/country record: USA. Florida: Miami-Dade county, Coral Gables, Montgomery Botanical Garden, 25.6572917 °N, 80.2805500 °W, Malaise trap, 15–26.ix.2016, T. Magellan, CNC819985 (1♂, CNC).

    Diagnosis: This species has only one pair of lateral scutellar setae, which will differentiate it most easily from the similar S. setipes Melander & Argo. The scutum also has one pair of large postsutural stripes that do not connect basally, the scutellum is entirely yellow, the brown marking on tergite 2 is concave anteromedially, and the surstylus is very short with a very shallow medial emargination that may not be readily visible. It belongs to the S. interrupta species group, characterized by male cerci that are not produced past the distal margin of the epandrium.

  2. Sobarocephala oculata Lonsdale & Marshall (Figure 2)

    New biogeographic region/country record: USA. Florida: Miami-Dade county, Coral Gables, Montgomery Botanical Garden, 25.6572917 °N, 80.2805500 °W, Malaise trap, 15–26.ix.2016, T. Magellan, CNC819970, CNC819998, CNC820011 (1♂ 2♀, CNC).

    Diagnosis: A brown scutellum and epandrium, and one pair of small, floating spots on the postsutural scutum are characteristic of this species. The surstylus is about as high as the epandrium, widest basally and broadly rounded apically, and male sternite 5 has a posteromedial comb of setae.

    To accommodate these new records in the key to Nearctic Sobarocephala provided by Lonsdale and Marshall (2007a), two sets of couplets must be emended, with newly added species in bold:

  3. First emendation:

    8. Scutellum entirely brown. … 8b

    8′. –Scutellum yellow, at least in part. … 9

    8b. Scutal stripe large, fused posteriorly along posterior margin of scutum. Frons sometimes with orange tint. Male abdomen entirely yellow. Eastern North America … S. dreisbachi Sabrosky & Steyskal

    8b′. –Stripes on scutum limited to one pair of small floating spots (Figure 2). Frons always yellow. Male abdomen with dorsomedial stripe and epandrium brown. USA (Florida), Cayman Islands … S. oculata Lonsdale & Marshall

  4. Second emendation:

    16. Postsutural stripe serrate on anterior margin. Scutellum brown laterally (rarely entirely yellow) (Lonsdale and Marshall [2007a: Figure 13]). Female tergite 6 yellow, sometimes with anteromedial spot. No small bristle in front of anterior dorsocentral. Surstylus deeply bifid (Lonsdale and Marshall [2007a: Figure 51]). Southeastern United States, Illinois … S. interrupta Sabrosky & Steyskal

    16′. –Postsutural stripe entire and rounded on anterior margin, if present. Scutellum usually entirely yellow, but if lateral corner brown (some S. setipes), small bristle present in front of anterior dorsocentral. Female tergite 6 brown, at least medially. Anterior lateral scutellar bristle not much smaller than posterior bristle, if at all. Surstylus rounded or with shallow, indistinct distomedial emargination. … 17

    17. One pair of lateral scutellar setae. Scutum with one pair of strong postsutural stripes (Figure 1). Fore tibia brownish. Tergite 2 with anteromedial margin of brown marking concave. Male sternite 5 without comb of setae. Surstylus with shallow, almost indistinct distomedial emargination (best viewed in posterior aspect). USA (Florida), Dominican Republic, Jamaica, Puerto Rico, and U.S. Virgin Islands, but also Brazil (Amazonas). … S. lucibilis Lonsdale & Marshall

    17′. –Two pairs of lateral scutellar setae. Scutum yellow postsuturally or with one pair of postsutural stripes that are usually strong. Fore tibia yellow. If brown marking on tergite 2 present, then anterior margin convex. Male sternite 5 with posteromedial comb of setae. Surstylus rounded … 17b

    17b. Notopleuron brown posteriorly (females sometimes with most of notopleuron and postpronotum brown) and scutum usually with one pair of wide brown postsutural stripes (Lonsdale and Marshall [2007a: Figure 15]). Acrostichal bristle absent. Length 2.4–2.9 mm. Female abdomen with wide brown stripe on tergites 2–6. Eastern North America … S. setipes Melander & Argo (in part)

    17b′. –Scutum yellow with dark brown quadrate spot on notopleuron (sometimes faded in males and teneral specimens) (Lonsdale and Marshall [2007a: Figure 16]). Acrostichal bristle present. Length 3.9–4.9 mm. Female abdominal pattern as follows: tergite 2 sometimes brown along posterior margin, tergites 3 and 4 with wide central stripe, tergite 5 with narrow central stripe, and tergite 6 dark brown. Eastern and central North America … S. lachnosternum Melander & Argo

Figure 1: 

Sobarocephala lucibilis Lonsdale & Marshall, Florida male; A: left lateral; B: dorsal; C: head, frontal. D–F: S. lucibilis, male genitalia (from Lonsdale and Marshall [2012: Figures 375–377]): D: external components, left lateral; E: same, posterior; F: internal components, left lateral.
Figure 1:

Sobarocephala lucibilis Lonsdale & Marshall, Florida male; A: left lateral; B: dorsal; C: head, frontal. D–F: S. lucibilis, male genitalia (from Lonsdale and Marshall [2012: Figures 375–377]): D: external components, left lateral; E: same, posterior; F: internal components, left lateral.

Figure 2: 

Sobarocephala oculata Lonsdale & Marshall, Florida male; A: left lateral; B: dorsal; C: head, frontal. D–F: S. oculata, male genitalia (from Lonsdale and Marshall [2012: Figures 515–517]): D: external components, left lateral; E: same, posterior; F: internal components, left lateral.
Figure 2:

Sobarocephala oculata Lonsdale & Marshall, Florida male; A: left lateral; B: dorsal; C: head, frontal. D–F: S. oculata, male genitalia (from Lonsdale and Marshall [2012: Figures 515–517]): D: external components, left lateral; E: same, posterior; F: internal components, left lateral.

Of the 19 Sobarocephala species now known from the Nearctic region, all but six have been collected in Florida. The absentees include Sobarocephala texensis Sabrosky & Steyskal, a Texas endemic, Sobarocephala pengellyi Lonsdale & Marshall from Georgia and Alabama, and the mostly or entirely northeastern species Sobarocephala atricornis Sabrosky & Steyskal, Sobarocephala lachnosternum, Sobarocephala latifacies Sabrosky & Steyskal, and Sobarocephala latifrons (Loew). Of these species, S. latifrons is widespread in the south and likely also occurs in Florida, and S. pengellyi likely also occurs in Florida because it is known from two adjacent states.

Nine species of Sobarocephala known from Florida are restricted to the Nearctic. Only Sobarocephala cruciger Sabrosky & Steyskal is known exclusively from Florida. Three other Florida species are known from other eastern coastal states: S. affinis, S. muesebecki (also Texas), and Sobarocephala wirthi Lonsdale & Marshall. More widespread eastern species are S. dreisbachi, Sobarocephala flava Melander & Argo, and Sobarocephala setipes, which extend as far north as Ontario and Quebec. Sobarocephala flaviseta (Johnson) is quite widespread in the Nearctic except for the western states and the continental north. Most records of Sobarocephala interrupta Sabrosky & Steyskal are from the southeastern United States, but one apparent outlier has been found in Illinois.

Four species known in Florida also occur in the Neotropics. Sobarocephala atrifacies Sabrosky & Steyskal is known from the Dominical Republic. Sobarocephala quadrimaculata Soós is known from Central America, the Caribbean, Alabama, Georgia, and Texas. S. lucibilis was previously known mostly from the Caribbean (Dominican Republic, Jamaica, Puerto Rico, and U.S. Virgin Islands) but it also has been recorded from Brazil (Amazonas). S. oculata was previously known from the Cayman Islands (Lonsdale and Marshall 2012).

The New World species of Clusiinae are represented by three species of the genus Clusia Haliday, one of which is western and two of which are northeastern. While none of these are known from Florida, the distribution of Clusia lateralis Walker extends relatively far south and may be found in or close to Florida following focused collecting. The species of Clusia are keyed in Lonsdale et al. (2011).

The Floridian Clusiodinae belong to three genera. Czernyola is known in Florida from C. concinna (Williston), which is widespread in the Neotropics, and C. weemsi (Lonsdale & Marshall), which also occurs in Jamaica, Mexico, and Peru. Czernyola annulipes (Johnson) likely occurs in Florida as it ranges from the Neotropics north to Maryland, Mississippi, North Carolina, and Texas. The New World Czernyola were revised by Lonsdale and Marshall (2006). Three Heteromeringia occur in Florida: Heteromeringia czernyi Kertész, which is widespread in the Neotropics; Heteromeringia flavipes Williston, which is known from Costa Rica, St. Vincent, and Nicaragua; and Heteromeringia nitida Johnson, which is widespread in the eastern Nearctic from northern Mexico to southern Ontario, but also occurs in parts of the southwestern USA. The New World Heteromeringia were revised by Lonsdale and Marshall (2007b). Clusiodes Coquillett is only represented in Florida by C. gracilolobus Caloren & Marshall, but the known distribution of C. johnsoni Malloch suggests that it may occur in Florida. The genus was revised in the New World by Caloren and Marshall (1998).

3.2 Other new global geographic records

3.2.1 Subfamily Clusiinae

  1. Clusia flava (Meigen)

    New country records: GEORGIA. Kakheti region, Lagodekhi Reserve, Mt. Kudigora, 5–15.v.2014, Malaise trap, G. Japoshvili, CNC1582079, CNC1582468, CNC1582469, CNC1582475, CNC1582505, CNC1582506 (4♂ 6♀, CNC), 23.v–13.vi.2014, CNC1583223 (1♀, CNC), 25.v–4.vi.2014, CNC1146431 (1♂, CNC), 5–15.vii.2014, CNC473399 (1♂, CNC), 25.viii–4.ix.2014, CNC1582772, CNC479719, CNC479733, CNC479761, CNC479762, CNC479780 (2♂ 4♀, CNC), 16–27.x.2014, CNC481821 (1♀, CNC) (specimens collected at 666 m a.s.l., 847 m a.s.l., 1,841 m a.s.l., and 2,559 m a.s.l.). SERBIA. Twenty three kilometer SE of Nova Varos, along creek, 43.4430472 °N, 19.8529722 °E, 1,014 m a.s.l., Malaise trap, 14–16.vi.2009, J. Skevington, CNC314483 (1♀, CNC).

    Comments: Four species herein are newly recorded for Georgia: Clusia flava, and Clusiodes albimanus (Meigen), C. gentilis (Collin) and C. pictipes (Zetterstedt). All four species are widespread and known from Russia and many European countries, but these Georgian records extend their known southern distribution. The Asian distribution of these taxa is poorly known, but accumulating distributional data suggest that these species will likely be found in most forested northern Palearctic areas. The extent of their southeastern boundaries into Korea and China will be interesting to determine.

  2. Clusia lateralis Czerny

    New province and state records: CANADA. Manitoba: Winnipeg, Beaudry Provincial Park, 49.8613333 °N, 97.47771667 °W, 230 m a.s.l., river-bottom forest, 21.vi.2015, B.J. Sinclair, CNC883041 (1 ex., CNC). USA. Indiana: Terre Haute, 39.4697222 °N, 87.3897222 °W, 11.v.1944, Fred C. Harmston & Verna H. Harmston, CNC882945 (1 ex., CNC), Maine: Dryden, 44.5864833 °N, 70.2099139 °W, G.H. Heinrich, CNC882942 (1 ex., CNC), Missouri: Williamsville, 36.9726389 °N, 90.5483083 °W, 14.vii.1969, Malaise trap, CNC883037 (1 ex., CNC).

    Comments: The specimen from Maine is unusual in that is almost entirely without pigment and the interfrontal setae are missing, and it does not appear as though these characteristics are an artifact of poor preservation or damage. The Manitoba record greatly extends the northwestern distribution of this species.

  3. Clusia occidentalis Malloch

    New state records: USA. Alaska: Juneau, 58.3280000 °N, 134.4190333 °W, 28.vi.1988, F. Brodo, CNC91399 (1 ex., CNC), Idaho: Kootenai county, Highway 97, St. Joe National Forest, FR 438, 47,6065333 °N, 116.6683167 °W, 660 m a.s.l., ex. Beauty Creek, 19.vi.2014, B.J. Sinclair, CNC883148 (1 ex., CNC), Latah county, Moscow Mountain, Moscow Mountain Road, 46.7953500 °N, 116.9015500 °W, 1,000 m a.s.l., ex. cascading stream, 22.vi.2014, B.J. Sinclair, CNC883146 (1 ex., CNC), Latah county, St. Joe National Forest, West of Laird Park, 46.9605167 °N, 116.5975333 °W, 855 m a.s.l., ex. meander stream, 22.vi.2014, B.J. Sinclair, CNC883147 (1 ex., CNC), Montana: Mineral county, Lolo NF, Trout Creek Campground, 47.1150500 °N, 114.8717500 °W, 917 m a.s.l., 26.vi.2017, B.J. Sinclair, CNC759017 (1 ex., CNC), New Mexico: Dona Ana county, Jornada Ecology Site, 40 km NNE, Las Cruces, 3.6166667 °N, 106.7500000 °W, top litter mesquite, 9.x.1986, E.E. Lindquist, CNC759018 (1♂, CNC).

    Comments: The Alaskan record reveals a much more extensive northwestern distribution than previously appreciated, and the other state records reveal a more extensive inland distribution. This species appears to be relatively abundant only from California to British Columbia, where it has been previously recorded.

3.2.2 Subfamily Clusiodinae

  1. Clusiodes albimanus (Meigen)

    New country records: BELARUS. Minsk region, Barysaw district, Vialikaje Stachava env., 54.1490222 °N, 28.6364833 °E, 161 m a.s.l., 7.vii.2013, D. Gavryushin, Jeff_Skevington_Specimen43885 (1 ex., CNC). GEORGIA. Kakheti region, Lagodekhi Reserve, Mt. Kudigora, Malaise trap, 5–15.v.2014, G. Japoshvili, CNC489509, CNC1582472 (2♀, CNC), 15–25.vi.2014, CNC474140, CNC474180 (2♀, CNC), 23.v–13.vi.2014, CNC474319, CNC488059 (2♀, CNC), 25.v–4.vi.2014, CNC1146435, CNC1146438, CNC1146441, CNC1146448 (1♂ 3♀, CNC), 4–14.vi.2014, CNC1582923 (1♀, CNC), 25.vi–5.vii.2014, CNC1583253, CNC1583309 (1♂ 1♀, CNC), 15–25.vii.2014, CNC1583109, CNC1582296 (1♂ 1♀, CNC), 5–15.viii.2014, CNC631158 (1♀, CNC), 25.viii–4.ix.2014, CNC1582721, CNC1582736, CNC1582753, CNC1582774, CNC1582777, CNC1582792, CNC1582795, CNC1582807, CNC479712, CNC479730, CNC479741, CNC479743, CNC479745, CNC479777 (8♂ 6♀, CNC), 5–14.ix.2014, CNC1147408, CNC1147438 (1♂ 1♀, CNC), 15–27.ix.2014, CNC631277, CNC631280 (1♂ 1♀, CNC) (specimens collected at 666 m a.s.l., 1,841 m a.s.l., 1,902 m a.s.l., 2,230 m, and 2,559 m a.s.l.).

  2. Clusiodes americanus Malloch

    New province/state records: CANADA. New Brunswick: Kouchibouguac National Park, 46.8516083 °N, 64.9710611 °W, 11.vii.1977, J.R. Vockeroth, Code-5583S, CNC881883 (1♀, CNC), Kouchibouguac National Park, 13.vii.1977, G.A. Calderwood, Code-5599I, CNC881882 (1♂, CNC). USA. Mississippi: Arg. Col., 4.v.1920, A. McIntosh, CNC1865978 (1♀, MEMU).

    Comments: These records extend the known northeastern and southwestern distribution of this species.

  3. Clusiodes gentilis (Collin)

    New country records: GEORGIA. Kakheti region, Lagodekhi Reserve, Mt. Kudigora, 41.8827333 °N, 46.3218500 °E, 1,841 m a.s.l., Malaise trap, 25.viii–4.ix.2014, G. Japoshvili, CNC1582719, CNC1582794 (2♂, CNC), 41.8524833 °N, 46.2877667 °E, 666 m a.s.l., 5–14.ix.2014, CNC1147422 (1♂, CNC), 41.9061833 °N, 46.334000 °E, 2,559 m a.s.l., 23.v–13.vi.2014, CNC1583249 (1♀, CNC).

  4. Clusiodes nitidus Melander & Argo

    New state records: USA. Colorado: Hinsdale county, Narrow Grade Creek, 2,652 m a.s.l., 38.1822222 °N, 107.3050000 °W, 15.vi.2017, S.E. Brooks, CNC854384 (1 ex., CNC), Summit county, Frisco, N. Tenmile Creek, 2,819 m a.s.l., 39.5752778 °N, 106.1180583 °W, Malaise trap near creek, 13–22.vi.2017, Cumming & Brooks, CNC854776 (1 ex., CNC).

  5. Clusiodes pictipes (Zetterstedt)

    New country records: GEORGIA. Kakheti region, Lagodekhi Reserve, Mt. Kudigora, 41.8524833 °N, 46.2877667 °E, 666 m a.s.l., Malaise trap, 23.iv–3.v.2014, G. Japoshvili, CNC1582261 (1♂, CNC), 25.vi–5.vii.2014, CNC1583181 (1♂, CNC).

  6. H. fumipennis Melander & Argo

    New country records: USA. Louisiana: Louisiana, Baton Rouge Par., Baton Rouge, Perkins Rd. Park, 27.ix.1992, J.T. McBride, LSAM306165 (1♀, LSAM).

    Comments: This new country record is represented by a single female. While the wing of this female is characteristic of the species, as is the pruinosity of the frons, coloration and other external morphological characters overlap with those of the similar H. nitida, and this species could represent previously unrecorded intraspecific variation. Heteromeringia fumipennis primarily occurs in the Neotropics where it is widespread, but it has been recorded in Nearctic Mexico (Lonsdale and Marshall 2007b).

3.2.3 Subfamily Sobarocephalinae

  1. Sobarocephala affinis (Johnson)

    New state records: USA. Alabama: (see Section 2.3 below for specimen details), Mississippi: Stone county, U.M. Forest Lands, 28.ix.1985, Paul K. Lago, CNC1865993 (1♀, MEMU).

  2. Sobarocephala cacumen Lonsdale & Marshall

    New state records: MEXICO. Oaxaca: Comaltepec, La Esperanza, 17.6266111 °N, 96.3695000 °W, 1,600 m a.s.l., edge of montane cloud forest, 1–6.x.2008, A. Lopez Garcia, CNC883762 (1♀, CNC), Comaltepec, La Esperanza, 17.6266111 °N, 96.3695000 °W, 1,600 m a.s.l., edge of montane cloud forest, 1–8.x.2008, A. Lopez Garcia, CNC759026, CNC883764 (2 ex., CNC).

  3. Sobarocephala flava Melander & Argo

    New state record: USA. Alabama: Monroe county, Clairborne Dam, 1 mile S, 31.5916667 °N, 87.5366667 °W, 29–30.v.1995, T.L. Schiefer, black light, CNC1865977 (1♀, MEMU).

  4. Sobarocephala fuscina Lonsdale & Marshall

    New country record: PANAMA. Canal Zone, Gatun, West Creek Trail, human feces, pitfall trap, 7–9.iv.1987, J.R. MacDonald, CNC1865979 (1♀, MEMU).

  5. Sobarocephala horologium Lonsdale & Marshall

    New country record: MARTINIQUE. 1 km E Diamant, 14.4783333 °N, 61.0100000 °W, 10 m a.s.l., ex. thorn forest, Malaise trap, 6–23.vii.2010, S. Peck, CNC607266 (1 ex. [abdomen missing], CNC).

  6. Sobarocephala lineola Lonsdale & Marshall

    New country record: PERU. Madre de Dios: Los Amigos Biological Station, 12.5691667 °S, 70.1001111 °W, 2–14.vi.2006, J. Klymko & S. Paiero, CNC635064, CNC635065 (2♂, CNC).

  7. Sobarocephala muesebecki Sabrosky & Steyskal

    New state records: USA. South Carolina: Chesterton county, Carolina Sandhills NWR, 34.562000 °N, 80.2106000 °W, Malaise trap, 3–17.v.2017, M. Caterino & M. Ferro, CUAC000047662 (1♀, CUAC), Mississippi: Oktibbeha county, Mississippi State North Farm, yellow pan trap, 30.viii–1.ix.1989, Jerry Baker, CNC1866011 (1♂, MEMU).

  8. Sobarocephala nigropilosa Lonsdale & Marshall

    New country record: PANAMA. Barro Colorado Island, Malaise trap, 18–27.xii.1996, M. vonTschirnhaus, L2319, CNC636639 (1♀, CNC).

  9. Sobarocephala synapta Lonsdale & Marshall

    New country record: SAINT VINCENT. Majorca, 13.2485500 °N, 61.1898639 °W, 457 m a.s.l., vii–viii.1972, (collector not given), CNC91491 (1 ex., CNC).

  10. Sobarocephala texensis Sabrosky & Steyskal

    New locality record: USA. Texas: Bandera, 29.7250000 °N, 99.0722222 °W, 31.x.1970, J. Morse, CNC1873623 (1♀, CUAC).

    Comments: While not a new state or country record, this female represents the first non-type specimen collected, found only 80 km from the type locality. Although the determination of a male would be definitive, the present female agrees with the type series except that the anterior region of the postgena is pilose.

  11. Sobarocephala wirthi Lonsdale & Marshall

    New state record: USA. Mississippi: Oktibbeha county, Dorman Lake, grasses, forbs, sweeping, 20.vi.1982, R.L. Brown, CNC1865982 (1♂, MEMU), Oktibbeha county, John Starr Memorial Forest, 33.3569444 °N, 88.8713889 °W, 24.v.1995, D.M. Pollock, CNC1865980 (1♂, MEMU), Smith county, Raleigh, 1 mi N, 14–15.vi.1985, R. Brown & G. Burrows, CNC1865981 (1♂, MEMU).

3.3 On the identity of S. muesebecki

The differences between S. affinis and S. muesebecki are slight, and females can be difficult to identify since the only unambiguous character differentiating them is the color of the epandrium, being yellow in S. affinis and dark brown in S. muesebecki. S. muesebecki sometimes also differs having slightly darker pigmentation on the wing, hind legs and setae, the anterior margin of the frons is sometimes whitish, and the gena and postgena are more frequently pilose (Lonsdale and Marshall 2007a). Alabama populations of S. muesebecki are additionally unique in having one pair of faded brownish spots anterolateral to the anterior dorsocentral setae in all examined females and some males, and a few of these spotted specimens also have a similar faded spot dorsomedially on the scutellum.

Despite the above differences, the two may be synonymous because their male genitalia are essentially identical and known distributions largely overlap. Additionally, specimens of both species within Alabama localities share a unique and previously unnoted character: an anteromedial abdominal stripe attaining the anterior extreme of tergite 1. The geographically restricted occurrence of this character suggests the possibility of localized variation within a single species.

Support for the separate specific status of these two species is still present in the subtle and variable differences listed above, however, as well as in the more striking difference of epandrium color. This strong binary feature of epandrium color is not seen elsewhere in the family, although some Sobarocephala exhibit more subtle color variants with intermediate forms. The collection of new material of both species across their distributions is recommended to obtain sequence data that may better establish species limits.

Material examined (affinis): USA. Alabama: Baldwin county, Bon Secour N.W. Ref. T9S.R2E, Sec. 24, Malaise trap, 13–14.x.1991, T. Schiefer & G. Eickwort, CNC1865983–1865990, CNC1865995–1865997 (3♂ 8♀, MEMU), Baldwin county, Bon Secour N.W. Ref. T9S.R2E, Sec. 25, on dunes, Malaise trap, 12–16.x.1991, T. Schiefer & G. Eickwort, CNC1865991, CNC1865992 (2♀, MEMU), Baldwin county, Bon Secour N.W.R., 30.2119444 °N, 87.8308333 °W, in fore dunes, black light, 8–9.viii.1994, R.L. Brown, CNC1865994 (1♀, MEMU).

Material examined (muesebecki): USA. Alabama: Baldwin county, Bon Secour N.W. Ref. T9S.R2E, Sec. 24, Malaise trap, 13–14.x.1991, T. Schiefer & G. Eickwort, CNC1866003 (1♀, MEMU), Baldwin county, Bon Secour N.W. Ref. T9S.R2E, Sec. 25, on dunes, Malaise trap, 12–16.x.1991, T. Schiefer & G. Eickwort, CNC1865998–1866002, CNC1866004–1866010 (7♂ 5♀, MEMU), Baldwin county, Oyster Bay, 1 mile E, T9S.R4E, Sec. 6, black light, 4.ix.1988, A.L. Brown & J. MacGown, CNC1866012, CNC1866013 (2♀, MEMU).


Corresponding author: Owen Lonsdale, Agriculture and Agri-Food Canada, 960 Carling Avenue, Ottawa, ON, K1A 0C6, Canada, E-mail:

Acknowledgments

Gary Steck (Florida Department of Agriculture and Consumer Services, Gainesville, Florida) is thanked for discussions on Florida Clusiidae. Photos were taken by Mackenzie Gamman at the CNC. The abstract was translated by J. Fernández-Triana. Loans were provided by Michael L. Ferro (CUAC), Victoria Bayless (LSAM), Terence Lee Schiefer (MEMU), Karen Wright (Texas A&M University), and Alex Wild (University of Texas, Austin). Stephen A. Marshall (University of Guelph, Guelph, Ontario) and Kevin Barber (Natural Resources Canada, Sault Ste. Marie, Ontario) are thanked for their thorough review of the manuscript.

  1. Research ethics: Not applicable.

  2. Author contributions: The author has accepted responsibility for the entire content of this manuscript and approved its submission.

  3. Competing interests: The author states no conflict of interest.

  4. Research funding: None declared.

  5. Data availability: Not applicable.

References

Caloren, D.C. and Marshall, S.A. (1998). A revision of the New World species of Clusiodes Coquillett (Diptera: Clusiidae). Stud. Dipterol. 5: 261–321.Suche in Google Scholar

Halbert, S.E. (2003). Entomology section. (Sobarocephala dreisbachi Sabrosky & Steyskal, a fly) p. 9. In: Anderson, P.J., and Dixon, W.N. (eds.). TRI-OLOGY 42: 3–9.Suche in Google Scholar

Lonsdale, O. (2017). World catalogue of the druid flies (Diptera: Schizophora: Clusiidae). Zootaxa 4333: 1–85, https://doi.org/10.11646/zootaxa.4333.1.1.Suche in Google Scholar PubMed

Lonsdale, O., Cheung, D.K.B., and Marshall, S.A. (2011). Key to the world genera and North American species of Clusiidae (Diptera: Schizophora). Can. J. Arthropod Ident. 14, https://doi.org/10.3752/cjai.2011.14.Suche in Google Scholar

Lonsdale, O. and Marshall, S.A. (2006). Revision of the New World species of Craspedochaeta Czerny (Diptera: Clusiidae). Zootaxa 1291: 1–101, https://doi.org/10.11646/zootaxa.1291.1.1.Suche in Google Scholar

Lonsdale, O. and Marshall, S.A. (2007a). Revision of the North American Sobarocephala (Diptera: Clusiidae, Sobarocephalinae). J. Entomol. Soc. Ontario 138: 65–106.Suche in Google Scholar

Lonsdale, O. and Marshall, S.A. (2007b). Revision of the New World Heteromeringia (Diptera: Clusiidae: Clusiodinae). Beiträge Entomol. 57: 37–80, https://doi.org/10.21248/contrib.entomol.57.1.37-80.Suche in Google Scholar

Lonsdale, O. and Marshall, S.A. (2012). Sobarocephala (Diptera: Clusiidae: Sobarocesphalinae)-subgeneric classification and revision of the New World species. Zootaxa 3370: 1–307, https://doi.org/10.11646/zootaxa.3370.1.1.Suche in Google Scholar

Thompson, F.C. (1999). Data dictionary and standards for fruit fly information database. Myia 9: 49–63.Suche in Google Scholar

Received: 2023-08-08
Accepted: 2023-12-08
Published Online: 2024-06-28

© 2024 the author(s), published by De Gruyter on behalf of the Florida Entomological Society

This work is licensed under the Creative Commons Attribution 4.0 International License.

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