Leptoconops (Holoconops) foulki Clastrier and Wirth
publication ID |
https://doi.org/10.5281/zenodo.6391684 |
publication LSID |
lsid:zoobank.org:pub:CBD29188-143B-44DF-BE21-1654D50D8621 |
DOI |
https://doi.org/10.5281/zenodo.6391728 |
persistent identifier |
https://treatment.plazi.org/id/E8511E53-FFCB-EF64-6A8A-FC24FA8CFBFD |
treatment provided by |
Felipe (2022-03-28 21:03:26, last updated by Plazi 2023-11-06 22:12:43) |
scientific name |
Leptoconops (Holoconops) foulki Clastrier and Wirth |
status |
|
Leptoconops (Holoconops) foulki Clastrier and Wirth View in CoL
( Fig. 21, 23, 24, 26 View Figures 20–26. 20 , 28, 32 View Figures 27–32 )
Leptoconops (Holoconops) foulki Clastrier and Wirth, 1978: 38 View in CoL (key; female, male; fig. antenna, palpus, spermathecae, male genitalia, gonostylus, palpus; California).
Leptoconops (Holoconops) kerteszi View in CoL , misidentified: Wirth 1952a: 113 (in part; key; female; male genitalia; biology). Fox 1955: 263 (key; taxonomy). Ryckman 1961 (jackrabbit host). Foulk 1967 (blood meal size). Sjogren and Foulk 1967 (biology). Foulk 1968 (biology). Wirth and Atchley 1973: 45 (in part; key; female, male; fig. female wing, head, genitalia, spermathecae, hind tibial comb, fore tarsomeres 1 and 2, male genitalia; biology).
Diagnosis. ( Table 13) Body blackish brown, femora and tibiae dark brown, fore tibiae slightly pale at tip, mid and hind tarsomeres 1 and all tarsomeres 2 pale brown; clypeus with four setae, median pair ≥0.8 as far apart from each other as from corresponding lateral setae and out-of-line distad of lateral setae by <0.3 their distance apart (as in Fig. 10 L View Figures 9–15. 9 . knowltoni); palpal segment 3 sensory pit as deep as wide, broadening internally on female; mid tarsomere 1 without submedian spine. Female: stigma triangular, pointed; antenna with 11 flagellomeres; flagellomere 11 without submedian black seta; flagellomere 4 hyaline sensory seta laterad of long black seta, in axial alignment with corresponding sensory setae on flagellomeres 5–10; palpal segment 3 sensory pit opening a third the diameter of the interior; hind tarsomere 3 ~1.7× longer than 5; spermathecae with caplike diverticulum; cerci>3× longer than wide ( Fig. 1 View Figures 1–2 ). Male: tergite 9 with distal shoulders abruptly narrowed to base of adjacent apicolateral processes, without dorsal process, ventro-posterior setae separated by ~2× as much as separation of apicolateral processes (as in Fig. 20 L View Figures 20–26. 20 . knowltoni); gonostylus with three ventral setae all within 0.4–0.6 of gonostylus length, apical lamelliform expansion only partly covering apical tooth; apical dilation of paramere with proximal tooth narrow, thumblike; tarsomere 5 basal seta short, erect, curved.
Distribution. Oregon, Montana, south to California, Nevada, Utah (Carbon, Garfield, Juab, Kane, Salt Lake, San Juan, Tooele, Uintah, Washington, Wayne, Weber counties).
Larval ecology. A larval habitat near the Salton Sea in Southern California was characterized by alkali or saline soil dominated by iodinebush ( Allenrolfea occidentalis ) and desert holly ( Atriplex hymenelytra Torrey ex S. Watson , Amaranthaceae ) ( Foulk 1969). Brenner et al. (1984a) clarified that the habitat also produced L. knowltoni .
Life cycle. Sjogren and Foulk (1967) found that, in the laboratory, undisturbed blood-feeding lasted 7–8 minutes; oviposition began ~88 h later; 70– 75 eggs were usually laid, which hatched in 2.5 d at ~32°C; and first generation adults emerged in ~24 d; and, in the wild, a generation was completed in <8 weeks in March–May in Southern California .
Adult behavior and vector potential. Known wild hosts are human ( Clastrier and Wirth 1978) and jackrabbit ( Lepus californicus Gray , Leporidae ) ( Ryckman 1961). Laboratory hosts include rabbits, mice, chicks, and humans ( Sjogren and Foulk 1967). Mullens and Dada (1992a) collected L. foulki from domestic rabbit ( Oryctolagus cuniculus ), Japanese quail ( Coturnix japonica ), and bighorn sheep ( Ovis canadensis nelsoni ), Furthermore, Foulk (1967) found the average replete blood meal to be 0.21 mg (0.20 μl).
Adults have been observed to alight on sunlit sand when its temperature drops to ~41 °C in late afternoon, rest within the top 4 mm of dry sand through the night and return to the surface when the temperature rises to ~18 °C in the morning ( Foulk 1968). I collected a female biting my ear midday on 23 April 2000 in Spanish Valley, Grand County (38.5274°N 109.4997°W), 7 km southeast of Moab.
Brenner et al. (1984a) reported host-seeking activity March–June, and females CO 2 -trapped in the same area in May had high parity rates (up to ~90%), suggesting a high vector potential. It is worth noting, however, that parity profiles are best interpreted along with knowledge of how prevalent autogeny is in the study population. We know little about the details of autogeny in biting midges, but it is quite possible that certain species have obligate autogeny, while others (or even populations within a species) express it at varying levels, based on aspects such as larval nutrition.
Symbionts. Leptoconops foulki ’s propensity to alight on and harbor within the top layer of sandy soil can explain Foulk’s (1968) observation of adults being preyed upon by Myrmeleon immaculatus De Geer antlions ( Neuroptera : Myrmeleontidae ) and parasitized by larval Microtrombidium mites ( Prostigmata : Microtrombidiidae ).
Remarks. Brenner et al. (1984a) discussed the difficulty distinguishing L. knowltoni from L. foulki because the color of the submedian black seta on flagellomere 11 of female L. knowltoni is often difficult to discern.
Brenner RJ, Wargo MJ, Mulla MS. 1984 a. Bionomics and vector potential of Leptoconops foulki and L. knowltoni (Diptera: Ceratopogonidae) in the lower desert of Southern California, USA. Journal of Medical Entomology 21: 447 - 459.
Clastrier J, Wirth WW. 1978. The Leptoconops kerteszi complex in North America (Diptera: Ceratopogonidae). United States Department of Agriculture Technical Bulletin 1573: 1 - 58.
Foulk JD. 1967. Blood meal size of Leptoconops kerteszi (Diptera: Ceratopogonidae). Mosquito News 27: 424.
Foulk JD. 1968. The resting behavior of the desert ceratopogonid, Leptoconops kerteszi. Journal of Medical Entomology 5: 223 - 229.
Foulk JD. 1969. Attack activity of two species of gnats in Southern California. Annals of the Entomological Society of America 62: 112 - 116.
Fox I. 1955. A catalogue of the bloodsucking midges of the Americas (Culicoides, Leptoconops and Lasiohelea) with keys to the subgenera and Nearctic species, a geographic index, and bibliography. Journal of Agriculture of University of Puerto Rico 39: 214 - 285.
Mullens BA, Dada CE. 1992 a. Insects feeding on desert bighorn sheep, domestic rabbits, and Japanese quail in the Santa Rosa Mountains of Southern California. Journal of Wildlife Diseases 28: 476 - 480.
Ryckman RE. 1961. Parasitic Ceratopogonidae and Simuliidae (Diptera) from Imperial County, California. Journal of Parasitology 47: 405.
Sjogren RD, Foulk JD. 1967. Colonization studies of Leptoconops kerteszi, biting gnats. Mosquito News 27: 394 - 397.
Wirth WW. 1952 a. The Heleidae of California. University of California Publications in Entomology 9: 95 - 266.
Wirth WW, Atchley WR. 1973. A review of the North American Leptoconops (Diptera: Ceratopogonidae). Graduate Studies Texas Tech University 5: 1 - 57.
Figures 20–26. 20) Leptoconops knowltoni male genitalia, ventral view, aedeagus (A), parameres (P), tergite 9 ventro-posterior setae (s), apicolateral processes (T9alp), gonostylus apical lamelliform expansion (Gsle). 21) L. foulki male genitalia, ventral view. 22) L. knowltoni gonostylus, ventral setae (vs). 23 L. foulki gonostylus. 24) L. foulki parameres (P), proximal tooth (t). Male tarsomere 5, basal seta (bS). 25) L. knowltoni. 26) L. foulki.
Figures 27–32. Female Leptoconops. 27) L. knowltoni flagellomeres 9–11, median black seta (s). Spermathecae (sp), diverticulum (d), neck (spn). 28) L. foulki. 29) L. americanus. 30) L. sublettei flagellomeres 3–6, flagellomere 4 seta bases (sb), hyaline sensory seta (hss). Palpal segment 3. 31) L. sublettei. 32) L. foulki.
Figures 9–15. 9) Leptoconops americanus female clypeus, setae (s). 10) L. knowltoni female clypeus. 11) L. knowltoni female palpal segment 3. 12) L. carteri female palpal segment 3 (Yolo County, CA). 13) L. werneri female tarsomeres 4–5 and claw (paratype, Imperial County, CA [UCRC]). 14) L. werneri male genitalia, ventral view, tergite 9 apicolateral processes (T9alp), meso-posterior lobe setae (s) (Riverside County, CA [UCRC]). 15) L. belkini male genitalia, ventral view, tergite 9 sclerotized lobe (L) (Riverside County, CA [UCRC]).
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.
Kingdom |
|
Phylum |
|
Class |
|
Order |
|
Family |
|
Genus |
Leptoconops (Holoconops) foulki Clastrier and Wirth
Phillips, Robert A. 2022 |
Leptoconops (Holoconops) foulki
Clastrier J & Wirth WW 1978: 38 |