Bibliographic record
Abstract
Zagrammosoma multilineatum (Ashmead) (Fig. 34) Hippocephalus multilineatus Ashmead, 1888: vii. Holotype ♀ [examined]. Locality: USA, Kansas, Riley Co., coll. C. Marlatt, host: Phyllonorycter ornatella (Lepidoptera: Gracillariidae). Depository: USNM type no. 27286. Zagrammosoma multilineatum; combination by Ashmead, 1904: 354. Preoccupied by Hippocephalus Swainson, 1839 (synonym of Percis Scopoli, 1777, Scorpaeniformes: Agonidae). Zagrammosoma multilineata punicea Girault, 1911: 123. Subspecies lectotype designation by Frison, 1927: 221. Lectotype locality: Washington D.C., USA. Lectotype depository: INHS type no. 44,261. Synonymy by Burks, 1979: 985. Zagrammosoma multilineatum puniceum; justified emendation by Peck, 1951: 460. Zagrammosoma multilineatum multilineatum (Ashmead, 1888). Subspecies designation by Peck, 1963: 189. Zagrammosoma multilineatus multilineatus; incorrect spelling by Pottinger & Le Roux, 1971: 437. Cirrospilus multilineatus; combination by Kerrich, 1969: 198. Cirrospilus (Zagrammosoma) multilineatum; unjustified use of subgenus designation by DeSantis, 1979: 261. Zagrammosoma zebralineata De Santis, 1983: 10. Holotype ♀ [examined]. Locality: Colombia, Pradera, coll. E. Flores, 1982. Depository: MLPA. Synonymy by Evans, 1999: 452. Diagnosis. Zagrammosoma multilineatum possesses dark stripes or bands that extend from the posterior margin of the pronotum to the notaulus (Fig. 34D), a character not found in other species of Zagrammosoma. The remaining body and wing patterns are similar to several species, however, the dark stripe between the notaulus and pronotum is absent in Z. interlineatum (Fig. 23D, E) and does not fully extend to the notaulus in Z. americanum (Fig. 4D, E) and Z. galapagoense (Fig. 18D, E). The gaster color patterns are different in Z. crowei (Fig. 12) and Z. interlineatum (Fig. 23). The second funicular is subequal in Z. deliae, as opposed to longer than wide in Z. multilineatum. There is no median stripe on the lower face in Z. interlineatum (Fig. 23A), whereas this stripe is present in Z. multilineatum (Fig. 34A). Description. Female - body length 1.4–1.98 mm. Metallic luster on body absent. Scape yellow with black stripe dorsally. Lower face with median stripe present. Vertex with 2 stripes above compound eye. Gena posteriorly with dark stripes below compound eye. Occiput yellow with 2 dark, vertical stripes. Pronotum with median stripe complete; laterally with 2 black stripes. Prepectus yellow with dark stripe along dorsal margin. Mesoscutum with median stripe complete. Mesoscutellum yellow with three dark stripes. Propodeum yellow with black median carina, anterior and posterior margins, and diagonal line connecting anterior and posterior margins. Procoxa and mesocoxa yellow. Metacoxa yellow with black stripe basally. Profemur and mesofemur yellow. Metafemur with interrupted or uninterrupted stripe dorsally. Fore wing: basal band absent; cubital band present; parastigmal, stigmal, and postmarginal bands present, with perpendicular extension greater than that of stigmal apex; connection from stigmal band to postmarginal band absent. Hind wing hyaline. Gaster yellow with dark transverse stripes and median stripe that bifurcates posteriorly on Gt 1. Upper ocular sulcus present. Pedicel longer than wide. Funiculars symmetrical: first longer than wide (w:l = 0.51–0.66); second longer than wide (w:l = 0.64–0.89). Pronotum, in dorsal view, bell-shaped (w:l = 1.07–1.45) 3–4 pairs of setae along posterior margin. Mesoscutum reticulate; small, scattered setae present; intermediate setae absent. Mesoscutellum subequal or wider than long (w: l = 1.0–1.13); submedian grooves absent or present, but faint and shallow. Hind tibial spur distinctly shorter than basitarsus. Hind basitarsus subequal or shorter than second tarsomere (bst:2 nd = 0.83–1.0). Fore wing l:w = 2.25–2.71. Submarginal vein with 5–6 setae dorsally. Basal fold setose. Cubital fold setose. Admarginal setae present. Uncus shifted basally more than length of uncus. Male - as female, except: body length 0.82–1.25 mm; metafemur yellow or yellow with interrupted or uninterrupted stripe dorsally; cubital band absent or present; gaster completely yellow or yellow with dark median stripe and transverse stripe on posterior margin of Gt 5. Remarks. No other species has been as difficult to define as Z. multilineatum, as the color patterns on the body and wings can be similar to many species. Extensive examination of loaned material revealed Z. multilineatum as the dumping ground for the genus, and at least six unique species have been identified from specimens identified as Z. multilineatum (Z. americanum, Z. deliae, Z. galapagoense, Z. interlineatum, Z. intermedium, Z. talitzkii). Published records of Z. multilineatum are difficult to verify without direct examination of the specimens used in published papers, and therefore, I have not included additional host and locality records of specimens for species that I have not personally examined. I have digitally examined the holotype of Z. zebralineatum and specimens collected by E. Flores from the same location and same host, coffee leaf miner (Leucoptera coffeella), and agree with the synonymy (Evans, 1999). Hosts. Reared from a large number of coleopteran, dipteran, and lepidopteran leaf miners. See Table 3 for a full list of hosts. Coleoptera: Buprestidae. Diptera: Agromyzidae. Hymenoptera: Tenthredinidae. Lepidoptera: Bucculatricidae, Gelechiidae, Gracillariidae, Lyonetiidae, Pyralidae, Tischeriidae. Distribution. Nearctic: Canada (BC), USA (AZ, CA, IA, KS, LA, MA, MD, MO, NC, NJ, NM, PA, SD, TN, TX, VA, VI). Neotropical: Bahamas, Jamaica, Colombia, Costa Rica, Ecuador (Galapagos), El Salvador, Guatemala, Haiti, Honduras, Venezuela (Fig. 35). Etymology. Multilineatum is taken from Latin meaning having many lines. Type material examined. Paratype: same as holotype [1♀, USNM: UCRCENT425376]. Additional material examined: BAHAMAS: Eleuthera: Rainbow Bay, 23m, 25°20’31”N, 76°27’1”W, 11.xi–19.xii.1986, J. R. Wiley, malaise [1♀, CNC: CNC 508660 (D5890)]. Exuma: Simon’s Point, 7m, 23°31’52”N, 75°47’49”W, 15–20.v.1986, T.L. McCabe [1♀, CNC: CNC 508842]. Grand Bahama Island: Freeport, Xanadu Beach, 26°29’35”N, 78°42’10”W, 16.x.1982, D. M. LaSalle, sand dunes [1♀, ANIC: UCRCENT238603]. CANADA: British Columbia: Chase, Adams Rd, 388m, 50°55’18”N, 119°37’45”W, 12.vii.1986, H. Goulet, car-net [1♀, CNC: CNC 508879]. COLOMBIA: Caldas: Naranjal, 1400m, 4°58’14”N, 75°39’4”W, 15.viii.1994, C. Lopez-Vaamonde, host: Leucoptera coffeella [1♁ 3♀, ANIC: UCRCENT238679–82]. Valle del Cauca: Palmira, 1015m, 3°30’31”N, 76°19’11”W, 15.ix.1975, A. Saldarriaga, host: Scrobipalpula sp., host plant: Solanum saponaceum (now bonariense?) [1♀, USNM: UCRCENT425392]. Valle Pradera, 1300m, 3°25’3”N, 76°11’36”W, 1981, E. Florez, #8106, host: Leucoptera coffeella, host plant: Coffee [4♁ 2♀, UCRC: UCRCENT414310, 499011–15]. Valle Pradera, 1982, E. Florez, host: Leucoptera coffeella, host plant: Coffee [MLPA-holotype of Z. zebralineatum]. COSTA RICA: Guanacaste: Area de Conservación Guanacaste, Murcielago, 75m, 10°56’28”N, 85°40’52”W, 24.i–4.ii.1996, J. Ugalde, malaise trap [1♀, ANIC: UCRCENT238683]. PN Santa Rosa, Sector Murcielago, Playa Blanca, 10m, 10°56’0”N, 85°51’0”W, 21.xi.2007, J. S. Noyes [1♁, BMNH: NHMUK10734428]. Santa Rosa NP, 300m, 10°53’33”N, 85°46’0”W, 2.iii.1986 – 23.iii.1986, D. H. Janzen, SE-8-C [1♁, USNM: UCRCENT425375]. Santa Rosa NP Hacienda (2C), 300m, 10°53’33”N, 85°45’59”W, 21.ii–14.iii.1987, D. Janzen, I. Gauld [1♀, BMNH: NHMUK10734425 (D5329)]. ECUADOR: Galapagos: Española Island, North Playa, 5–20m, 1°20’57”S, 89°41’51”W, 27.iv.1991, J. Heraty, arid zone, H91-002 [1♁ 9♀, UCRC: UCRCENT436418–436427]. Genovesa Island, Bahia Darwin, 20m, 0°19’8”N, 89°56’55”W, 10–27.iii.1992, S. Peck, Bursera forest, FIT, 92-14 [1♀, UCRC: UCRCENT410517]. Isabela Island, Alcedo, NE Playa, 0m, 0°20’40”S, 91°02’50”W, 26.vi.1991, J. Heraty, arid ravine, H91-120b [2♀, UCRC: UCRCENT491727, 491728]. Marchena Island, Punta Espejo, 0°18’54”N, 90°24’33”W, 11–24.iii.1992, S. Peck, 92-19 [1♀, UCRC: UCRCENT410522]. Pinzon Island, 2.5 km W. Pl. Escondida (5km on label), 280m, 0°36’14”S, 90°40’13”W, 19.vi.1991, J. Heraty, arid forest, H91-101 [3♀, UCRC: UCRCENT491724–26]. Santa Cruz Island, 1.5 km N. Bellavista, 280m, 0°40’55”S, 90°19’25”W, 1.vii.1991, J. Heraty,agricultural, H91-124 [1♀, UCRC:UCRCENT491721]. 13 km N. Santa Rosa, 300m, 0°34’6”S, 90°20’43”W, 1–30.iv.1992, S. Peck, arid zone, Bursera forest, FIT, 92-81 [1♀, UCRC: UCRCENT410519]. 6 km N. Los Gemelos, 300m, 0°34’37”S, 90°20’42”W, 17.v.1991, J. Heraty, low transition, H91-039 [1♀, UCRC: UCRCENT491722]. Santiago Island, 12 km E. Playa Espumilla, 725m, 0°13’54”S, 90°46’3”W, 5.vi.1991, J. Heraty, elfin forest, H91- 078 [1♁ 1♀, UCRC: UCRCENT491714, 491715]. EL SALVADOR: San Salvador, 690m, 13°42’29”N, 89°12’25”W, 18.v.1953, P.A. Berry, host: Leucoptera coffeella [2♀, USNM: UCRCENT425413, 425414]. GUATEMALA: West Guatemala, 460m, 14°33’2”N, 91°26’10”W, G. Manglitz, (Could be anywhere in “West Guatelama”), 51-6316, host: Leucoptera coffeella [6♁ 7♀, USNM: UCRCENT425379–91]. Retalhuleu: San Sebastian, 312m, 14°33’38”N, 91°39’12”W, ii–iii.1951, Oakley-Roberts, 51-2862, host: Leucoptera coffeella, host plant: Coffee [1♀, USNM: UCRCENT425416]. HAITI: 18°35’52”N, 72°11’45”W, 14.ii.1936, F. Sein Jr., Det. Lot No. 36- 4880, host: Leucoptera coffeella [2♁ 8♀, USNM: UCRCENT425402–10, 425412]. HONDURAS: Atlantida Dept.: La Ceiba, 15°46’7”N, 86°47’32”W, 6.vi.1991, R. Cave, host: Gracillaridae, host plant: Gliricidia sepium [1♀, ANIC: UCRCENT238605]. JAMAICA: Saint Andrew Parish: College Common, 173m, 17°59’54”N, 76°44’53”W, 1984, CIBC Trinidad Lot 5, CIE A16067, host: Leucoptera coffeella [1♀, BMNH: NHMUK10370145]. MEXICO: Baja California Sur: Las Barracas, 975m, 23°28’25”N, 109°27’8”W: 15.iv.1984, P. DeBach, Pan trap [1♀, UCRC: UCRCENT499001]; 17.iv.1985, P. DeBach, Pan trap
Fetched live from OpenAlex and de-inverted. Abstracts are not stored in this database: the inverted indexes are 8.6 GB of the frame’s 9.3 GB of text, and the host has 13 GB free.
How this classification was reachedexpand
Full frame machine prediction
Teacher imitationNot calibrated prevalence, not ground truth. Human validation pending. The Gemma side is a direct model label for every work in the frame, read from the title-only record. The Codex side is a classifier learned from the 10,348 direct Codex labels and calibrated to design-weighted sample rates; fields without enough sample support carry no Codex call. Candidate is the union of the two sides; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels.
Distilled classifier scores by category (both heads)
| Category | Codex | Gemma |
|---|---|---|
| Metaresearch | 0.000 | 0.000 |
| Meta-epidemiology (narrow) | 0.000 | 0.000 |
| Meta-epidemiology (broad) | 0.000 | 0.000 |
| Bibliometrics | 0.001 | 0.000 |
| Science and technology studies | 0.001 | 0.000 |
| Scholarly communication | 0.000 | 0.001 |
| Open science | 0.000 | 0.001 |
| Research integrity | 0.000 | 0.000 |
| Insufficient payload (model declined to judge) | 0.010 | 0.003 |
Machine scores (provisional)
The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.
Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.
score_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from itClassification
machine, unvalidatedMachine predicted; a candidate call from one source (direct Gemma or distilled Codex), not a consensus.
How this classification was reached, model by model and score by score, is at the end of the page under "How this classification was reached".