Lasioglossum (Sphecodogastra) boreale Svensson, Ebmer, and Sakagami 1977
publication ID |
https://doi.org/ 10.11646/zootaxa.3672.1.1 |
publication LSID |
lsid:zoobank.org:pub:2F022557-512C-4372-AD72-FF83302FBCC2 |
persistent identifier |
https://treatment.plazi.org/id/E56C0D52-FF96-0A50-FF79-DC91FF771A9D |
treatment provided by |
Felipe |
scientific name |
Lasioglossum (Sphecodogastra) boreale Svensson, Ebmer, and Sakagami 1977 |
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Lasioglossum (Sphecodogastra) boreale Svensson, Ebmer, and Sakagami 1977 View in CoL
( Figs. 5M View FIGURE 5 , 43B View FIGURE 43 , 44B View FIGURE 44 , 45B View FIGURE 45 , 46B View FIGURE 46 , 53 View FIGURE 53 , 54 View FIGURE 54 , 79C View FIGURE 79 , 81A View FIGURE 81 , 85A View FIGURE 85 , 87A View FIGURE 87 , 88B View FIGURE 88 )
Lasioglossum (Evylaeus) boreale Svensson et al. 1977, p. 219 View in CoL ♂ Holotype. ♂ Sweden, Torne Lappmark , Abisko, 3.viii.1973 (B. G. Svensson) on Chamaenerion angustifolium View in CoL [ZMU].
Evylaeus borealis (in Sakagami & Toda 1986. first record for Nearctic region)
Evylaeus (Fratevylaeus) borealis (in Pesenko 2007a: subgeneric classification)
Lasioglossum (Evylaeus) boreale (in Murao & Tadauchi 2007: redescription ♀ ♂)
Diagnosis. Female L. boreale can be recognised by the combination of head round (L/W ratio = 0.98–1.00) ( Fig. 43B View FIGURE 43 ); mesepisternum finely rugulose (as in Fig. 76D View FIGURE 76 ); inner metatibial spur pectinate-denticulate, teeth shorter than width of rachis ( Fig. 5M View FIGURE 5 ); propodeum with lateral carina fine, often not extending to dorsal margin, oblique carina fine (these carinae often so weak as to be difficult to discern) ( Fig. 79C View FIGURE 79 ); and T1 polished due to lack of microsculpture ( Fig. 81A View FIGURE 81 ). In the east, L. boreale is most similar to L. quebecense , L. comagenense , and L. seillean , all of which have strong, well-defined propodeal carinae ( Figs. 79 View FIGURE 79 D-F). Lasioglossum quebecense and L. seillean both have long teeth on the inner metatibial spur, distinctly exceeding the width of the rachis ( Figs. 5O, 5P View FIGURE 5 ) and T1 dull due to microsculpture. The female of L. comagenense has a shorter head (L/W ratio = 0.93–0.96) ( Fig. 43C View FIGURE 43 ).
Male L. boreale can be recognised by the combination of clypeus with yellow on distal half ( Fig. 44B View FIGURE 44 ); mandible short, not extending much beyond opposing clypeal angle; metasomal sterna nearly bare, hairs present but very short ( Fig. 85A View FIGURE 85 ); S2–S3 with dense punctures ( Fig. 88B View FIGURE 88 ); and basitarsi bright yellow ( Fig. 54 View FIGURE 54 ). The unique shape of the retrorse lobe ( Figs. 46B View FIGURE 46 ; 87A View FIGURE 87 ), which is short, subequal in length to gonostylus, is the most reliable character for distinguishing L. boreale males from those of L. comagenense , L. quebecense , and L. seillean ( Figs. 87B, 87C, 87D View FIGURE 87 ). The dense sternal punctures should also distinguish it from these three species ( Fig. 88 View FIGURE 88 ).
Redescription. FEMALE. Length 5.9–6.4 mm. Head length 1.72–1.79 mm. Head width 1.72–1.80 mm. Wing length 4.9–5.2 mm. (n=4)
Colour. Head and mesosoma black. Antenna black, except ventral surface of flagellum pale brown-orange. Tegula dark reddish brown. Legs dark brown, except medio- and distitarsi reddish brown. Wing membrane hyaline, faintly dusky. Pterostigma orange-brown. Metasomal terga black-brown, apical margins pale brown.
Structure. Head round (L/W ratio = 0.98–1.00). Clypeus ¾ below suborbital line. Eyes convergent below (UOD:LOD = 1.07–1.13). Gena subequal to eye width. Ocelli normal. Pronotum smoothly rounded. Protibial spur with apical serrations as long as width of malus. Inner metatibial spur pectinate, teeth 4–6, basal teeth shorter than width of rachis. Propodeal lateral carina reaching dorsal margin, oblique carina low, sometimes obscure, separating dorsolateral slope from posterior surface.
Surface sculpture. Supraclypeal area polished medially, punctures sparse (i=1–1.5d). Gena lineolate, postgena smoother. Mesoscutum imbricate; punctures dense (i≤d), except posteromedially (i=1–1.5d). Mesepisternum finely rugulose, smoother ventrally. Metapostnotum carinate-rugose. Propodeum imbricate-tessellate. Metasomal terga mostly coriarious, T1 polished; punctures dense, sparser posteromedially, T2 apical impressed area impunctate medially.
Pubescence. Head and mesosoma with sparse plumose hairs. Metafemoral scopa with dense plumose hairs. Metasomal terga with relatively dense, medially-interrupted apical fimbriae. T1 with sparse, erect plumose hairs. T2–T4 basolaterally with sparse, tomentum.
MALE. Length 6.7–7.5 mm. Head length 1.82–1.98 mm. Head width 1.69–1.90 mm. Wing length 4.5–5.2 mm. (n=4)
Colour. Head and mesosoma black. Clypeus yellow on apical half. Mandible brown. Labrum yellow, at least basally. Antenna black, except ventral surface of flagellum orange, less so on F10–F11. Legs dark brown, except tarsi, bases and apices of tibiae yellow, anterior surface of protibia yellow-testaceous. Wing membrane hyaline. Pterostigma brown. Metasomal terga dark brown.
Structure. Head long (L/W ratio = 1.04–1.10). Clypeus ¾ below suborbital line. Mandible short, reaching opposing clypeal angle. Flagellomeres, except F1 elongate, F2 longer than F1 and pedicel combined, subequal to scape. Eyes convergent below (UOD:LOD = 1.34–1.39). Gena narrower than eye. Pronotum smoothly rounded. Propodeal lateral carina nearly reaching dorsolateral slope.
Surface sculpture. Supraclypeal area imbricate, with sparse, shallow punctures (i=1–1.5d). Gena lineolate. Mesoscutum imbricate, reticulate anterolaterally; punctures dense (i≤d) but clearly separated medially (i=1–1.5d). Mesepisternum rugulose, weakly so ventrally. Metapostnotum anastomosingly rugose. Propodeum rugulose, posterior surface rugose. Metasomal terga polished; punctures deep, close basally. T2–T6 apical impressed areas impunctate. Metasomal sterna with distinct, deep punctures (i=1–1.5d).
Pubescence. Head and mesosoma with sparse plumose hairs. Face below antennal sockets with dense tomentum, clypeus bare on distal half. Propodeum largely bare, with scattered plumose hairs. Metasomal terga nearly bare, without apical fimbriae. T2 with narrow, basolateral patch of tomentum. Metasomal sterna nearly bare, with sparse, short, plumose hairs (<1 OD).
Terminalia . As shown in Figs. 45B View FIGURE 45 , 46B View FIGURE 46 , 87A View FIGURE 87 . Gonostylus small, with short setae. Retrorse lobe short, length subequal to gonostylus ( Fig. 87A View FIGURE 87 ).
Taxonomic notes. Lasioglossum boreale belongs to the fulvicorne-fratellum species-group ( Ebmer 1974; Svensson et al. 1977), equivalent to the subgenus Evylaeus (Fratevylaeus) of Pesenko (2007a). It is the only member believed to have a Holarctic distribution ( Svensson et al. 1977). The range of the species is limited to alpine and boreal regions from the type locality in Sweden to mountain ranges in the south-western USA. In the east, it has been recorded from high elevations in New Hampshire as well as high latitudes ( Packer & Taylor 2002; see below). There is genetic variation across geographic localities, particularly high elevation sites in the southwestern USA, but the New Hampshire population doesn’t differ greatly from those in arctic regions of North America ( Packer & Taylor 2002). It is possible that L. boreale is in fact three or more species ( Packer & Taylor 1997, 2002). Additional studies of L. boreale across its range, with comparison to other North American fulvicorne-fratellum group species would be beneficial. The southwestern species L. dasiphorae ( Cockerell 1901b) , known from the Las Vegas Range in New Mexico, is similar to L. boreale , but the type specimen has a longer head (L/W ratio = 1.05) than specimens of L. boreale we measured, although this may be within the range of variation for this species ( Sakagami & Toda 1986).
Biology. This species is a polylectic ground-nester ( Svensson et al. 1977). Nests excavated in Sweden had a single female ( Svensson et al. 1977). The species is only known from high latitudes and altitudes that presumably preclude the formation of annual eusocial colonies.
DNA barcodes. Twenty-eight specimens were sequenced (maximum intraspecific p-distance: 0.9%). The minimum p-distance between L. boreale and L. comagenense is 1.2%. Lasioglossum boreale differs from the other fulvicorne-fratellum species included here by three fixed substitutions: 321(G), 405(C), and 621(G) (see Table 2).
Range. Fig. 55 View FIGURE 55 .
Material examined. 120 (56 females, 64 males). Deposited in BBSL, CNC, CUIC, PCYU, PMAE, and ROMent. For additional records see Svensson et al. 1977 and Packer and Taylor 2002.
CANADA. ALBERTA: Kananaskis, forest reserve; Division 3: Waterton Lake N.P., Cardston Entrance ; BRITISH COLUMBIA: Similkameen Reg.: Hedley; Stikine Reg.: Atlin; Vancouver Is.: Mesachie Lake, Arbutus Hill; Miracle Beach, nr. Oyster River ; MANITOBA: Northern Reg.: Fort Churchill; Churchill, Akuldilk; Churchill, bus stop; Churchill, Krumholz Tundra; Churchill, Ramsay Creek ; Churchill, Twin Lakes Cabins ; NORTHWEST TERRITORIES: Inuvik Reg. : Inuvik ; YUKON TERRITORY: Rampart House ; Snag .
JAPAN. Hokkaido: Sugatami —no—ike, Mts. Taisetsuzan , 1600 m .
USA. ALASKA: Bristol Bay Borough: King Salmon, Naknek R.; Naknek ; NEW HAMPSHIRE: Coos Co.: Mt. Washington, Alpine Garden; Mt. Washington, 4500 ft [1372 m] . WYOMING: Albany Co.: 10,000 ft [3048 m] .
No known copyright restrictions apply. See Agosti, D., Egloff, W., 2009. Taxonomic information exchange and copyright: the Plazi approach. BMC Research Notes 2009, 2:53 for further explanation.
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Lasioglossum (Sphecodogastra) boreale Svensson, Ebmer, and Sakagami 1977
Gibbs, Jason, Packer, Laurence, Dumesh, Sheila & Danforth, Bryan N. 2013 |
Lasioglossum (Evylaeus) boreale
Svensson, B. G. & Ebmer, A. W. & Sakagami, S. F. 1977: 219 |