Rothaeina jamesi Bennett, 2023
publication ID |
https://doi.org/ 10.11646/zootaxa.5318.1.5 |
publication LSID |
lsid:zoobank.org:pub:161E8842-5DB1-40CA-A4B7-2287462D86E1 |
DOI |
https://doi.org/10.5281/zenodo.8158353 |
persistent identifier |
https://treatment.plazi.org/id/03BF87AB-E43C-0700-09BE-F4FA6164FCDC |
treatment provided by |
Plazi |
scientific name |
Rothaeina jamesi Bennett |
status |
sp. nov. |
Rothaeina jamesi Bennett spec. nov.
Figs 43–44 View FIGURES 43–52 , 53 View FIGURES 53–59 , 60–62 View FIGURES 60–65 , 70–72 View FIGURES 70–74 , 85 View FIGURES 84–86
Type material. U.S.A.: California: Holotype male. Del Norte County, 3 miles east of Klamath , 16.ix.1961, W. Ivie & W.J. Gertsch ( AMNH) . Paratypes: U.S.A.: California: Del Norte , 5♀, 3 mi. E of Klamath, 16.ix.1961, W. Ivie & W.J. Gertsch ( AMNH) ; 2♀, 10–15 mi. E of Fort Dick , 29.v.1952, V.D. Roth ( CAS) ; Humboldt, 3♀, Avenue of the Giants, Ten-Taypo Trail [Prairie Creek Redwoods State Park], 14.ix.1971, V.D. Roth ( CAS) ; 2♀, 6 mi. N of Hoopa , 22.viii.1959, W.J. Gertsch & V.D. Roth ( AMNH) ; 3♀, Orick , 16.ix.1961, W. Ivie & W.J. Gertsch ( AMNH) ; 1♀, 5 mi. SW of Orleans , 22.viii.1959, W.J. Gertsch & V.D. Roth ( AMNH) ; 1♀, Redwoods National Forest, Bald Hills Rd. off Hwy 101, 24.ix.2003, P. Paquin & D. Wytrykush ( RBCM) ; 4♁ 2♀, Rhododendron Trail along Hwy 101, Prairie Creek Redwoods State Park , 30.vi.2006, J. Ledford & S. Synhorst ( CAS) . Oregon: Curry, 2♀, 7 mi. E of Brookings, Chetco River , 29.iv.1952, V.D. Roth ( CAS) .
Etymology. The specific name is a patronym honouring the late Elmore James who set the standards for electric slide guitar blues in post-World War II Chicago, U.S.A.
Diagnosis. The male of R. jamesi spec. nov. is distinguished from the males of the three other species of Rothaeina gen. nov. with known males ( R. mackinleyi spec. nov., R. petersoni spec. nov., and R. sequoia comb. nov.) by a combination of characters of the patellar apophysis, the medial component of the retrolateral tibial apophysis, and the proximal arm of the tegular apophysis. In the male of R. jamesi spec. nov. the patellar apophysis ( Figs 53 View FIGURES 53–59 , 62 View FIGURES 60–65 ) is slender and elongate (length about 2/3 width of the patella), smoothly tapering, and strongly dorsad and terminates in a single large peg seta; the medial component of the retrolateral tibial apophysis ( Figs 53 View FIGURES 53–59 , 61 View FIGURES 60–65 ) is a short and slender rigid spine-like process; and the proximal arm of the tegular apophysis ( Figs 43 View FIGURES 43–52 , 60 View FIGURES 60–65 ) is bulky, blunt, and angular in ventral view. In the other species with known males the patellar apophysis is relatively stubby and short (length no more than 1/2 width of patella) and has two to several terminal peg setae ( R. mackinleyi spec. nov., Figs 54–55 View FIGURES 53–59 ; R. petersoni spec. nov., Figs 56–57 View FIGURES 53–59 , 64–65 View FIGURES 60–65 ; and R. sequoia comb. nov., Figs 58–59 View FIGURES 53–59 ); the medial component of the retrolateral tibial apophysis is a longitudinal ledge ( R. mackinleyi spec. nov., Fig. 54 View FIGURES 53–59 ), greatly reduced and marked by a single basally articulated macroseta ( R. petersoni spec. nov., Figs 56–57 View FIGURES 53–59 ), or a very slender and elongate rigid spine-like process ( R. sequoia comb. nov., Figs 58–59 View FIGURES 53–59 ); and the proximal arm of the tegular apophysis is variously developed but always with a more-or-less acuminate tip ( R. mackinleyi spec. nov., Figs 45–47 View FIGURES 43–52 ; R. petersoni spec. nov., Figs 48–49 View FIGURES 43–52 ; and R. sequoia comb. nov., Figs 50–51 View FIGURES 43–52 ).
The females of R. jamesi spec. nov. are most likely to be confused with those of R. mackinleyi spec. nov.; separating the females of these two species from the females of the other species of Rothaeina gen. nov. is discussed in the diagnosis of R. beaudini spec. nov. From the females of R. mackinleyi spec. nov. the females of R. jamesi spec. nov. usually may be distinguished by the greater complexity of the spermathecal ducts characterized by a small additional loop posteriorly in each spermatheca, close to the fertilization duct ( Figs 71–72 View FIGURES 70–74 ) versus additional loop absent in the spermathecae of females of R. mackinleyi spec. nov. ( Figs 73–74 View FIGURES 70–74 ). Note also the caveat in the first paragraph of the diagnosis of R. beaudini spec. nov.
Description. As in diagnosis and description of the genus. Additional descriptive characters presented here. Abdomen usually at least lightly patterned.
Male: (n=5). Patellar apophysis ( Figs 53 View FIGURES 53–59 , 62 View FIGURES 60–65 ) with one large peg seta at tip, three smaller ones dorso-basally. Distal component of retrolateral tibial apophysis ( Fig. 53 View FIGURES 53–59 ) slightly extended distally over base of cymbium. Tegular apophysis ( Figs 43–44 View FIGURES 43–52 , 60 View FIGURES 60–65 ) with small basal outgrowth; distal arm long, relatively narrow (length about twice width); proximal arm elongate, ventrad, blunt in ventral view, acuminate in retrolateral view.
Measurements (n=1). Holotype CL 2.20, CW 1.75, SL 1.21, SW 1.12.
Female: (n=21). Atrium a single transverse inconspicuous slit anteromedially located on epigyne ( Figs 70, 72 View FIGURES 70–74 ). Vulva ( Figs 71–72 View FIGURES 70–74 ) with width usually less than 3.5 times atrial height (measured from epigastric groove to atrium); copulatory ducts distinctly separated at atrium; spermathecal heads near anterior margin of vulva; medial transverse section of spermathecae a prominent feature in dorsal cleared view; Bennett’s glands medially located on spermathecae (visible in dorsal view of cleared vulva).
Measurements (n=18). CL 1.65–2.23 (1.93+0.18), CW 1.25–1.65 (1.47+0.14), SL 0.88–1.22 (1.05+0.09), SW 0.81–1.13 (0.99+0.09).
Distribution and natural history. ( Fig.85 View FIGURES 84–86 ). Rothaeina jamesi spec. nov. is endemic to a small area encompassing extreme southwestern Oregon, U.S.A., south to Humboldt County in northwestern California, U.S.A. and, within that restricted area, the species appears to be relatively common with records of males and females occurring in the early 2000s. Males have been collected in mid-September (holotype) and early June.
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.