Bibliographic record
Abstract
Neoceruraphis viburnicola (Gillette, 1909) (Figs. 40–73; Tabl. 4–5) Aphis viburnicola Gillette, 1909: 280 [Davis 1910: 492; Gillette & Bragg 1915: 102; Gillette & Bragg 1918: 329; Guyton 1924: 14; Hottes 1931: 64; Hottes & Frison 1931: 223; Gillette & Palmer 1932: 452; Burnham 1938: 187; Knowlton 1941: 67; Palmer 1952: 184] Aphis viburnum Scopoli in Wilson 1910: 29 Anuraphis viburnicola (Gillette, 1909) in Patch 1923: 298 [Cutright 1925: 192; Leonard 1963: 66] Ceruraphis viburnicola (Gillette, 1909) in Börner 1926: 226 [Shaposhnikov 1950: 215; Börner 1952: 96; Börner & Heinze 1957: 139; Eastop & Hille Ris Lambers 1976: 133; Smith & Parron 1978: 74; Robinson 1979: 25; Chakrabarti & Medda 1985: 129; Smith & Eckel 1996: 49; Remaudière & Remaudière 1997: 86; Zhang & Chen 1999: 267; Maw et al. 2000: 18; Kaygin et al. 2010: 2] Yezabura (Ceruraphis) eriophori (Walker, 1848) in Börner & Schilder 1932: 585 Neoceruraphis viburnicola (Gillette, 1909) in Shaposhnikov 1956: 285 [MacGillivray 1960: 704; Gittins et al. 1976: 20] Material. 1 fundatrix, 6 emigrants, 11.vi.1909, USA, Colorado, Fort Collins, Viburnum sp. (metatype) (from collection of ZIN RAS); 1 male, 6 gynoparae, 12.x.1913 and 22.x.1913, USA, Colorado, Fort Collins, Viburnum opulus (from collection of MNHN); 1 emigrant, 24.v.1927, USA, Utah, Providence, Viburnum opulus (from collection of MNHN); 1 fundatrix, 6 emigrants, 6.vi.1938, USA, Colorado, Fort Collins, Viburnum opulus (from collection of NHM); 3 fundatrices, 21.iv.1957, USA, Utah, Moab, Viburnum sp. (from collection of NHM); 2 emigrants, 22.v.1958, USA, Utah, Brigham City, Viburnum opulus (from collection of NHM); 2 emigrants, 19.vi.1958, Canada, New Brunswick, Kingsclear, Viburnum trilobum Marshall (from collection of ZIN RAS); 3 gynoparae, 1 male, 3.x.1958, USA, Utah, Providence, taken flying (from collection of NHM); 1 male, 15.x.1958, USA, Utah, Logan Canyon, sweeping (from collection of NHM); 2 fundatrices, 26.v.1960, Canada, New Brunswick, Fredericton, Viburnum trilobum (from collection of ZIN RAS); 4 apterous viviparous females, 27.vi.1960, Canada, New Brunswick, Fredericton, Carex sp. (in culture) (from collection of ZIN RAS); 1 gynopara, 1 male, 21.x.1960, Canada, New Brunswick, Fredericton, Viburnum sp. (from collection of ZIN RAS); 3 gynoparae, 24.ix.1964, USA, Utah, Logan, taken flying (from collection of NHM); 1 emigrant, 17.vi.1965, USA, Manitoba, Winnipeg, Viburnum lentago L. (from collection of NHM); 1 gynopara, 16.x.1965, USA, Iowa, Ames, suction trap (from collection of MNHN); 6 emigrants, 5.vi.1966, USA, Pennsylvania, State College, Viburnum opulus (from collection of NHM); 10 gynoparae, 26.viii.1976, Canada, Québec, Saint-Gédéon, Viburnum sp. (from collection of MNHN); 9 gynoparae, 9 and 15.ix.1976, USA, Maine, Orono, Viburnum opulus and Viburnum sp. (from collection of MNHN); 1 gynopara, 13 oviparous females, 2.xi.1976, USA, Maine, Orono, Viburnum sp. (from collection of MNHN); 1 oviparous female, 31.x.1977, Canada, British Columbia, Vancouver, Viburnum trilobum (from collection of MNHN); 2 emigrants, 7.vi.1984, USA, Utah, Logan, Viburnum sp. (from collection of MNHN); 1 emigrant, 6.v.1986, USA, Idaho, Notus, Viburnum sp. (from collection of MNHN); 8 emigrants, 26 and 29.vi.1984, USA, Utah, Logan, Viburnum sp. (from collection of MNHN); 1 gynopara, 29.ix.1989, USA, Manitoba, Winnipeg, Kings Drive Park, Viburnum sp. (from collection of MNHN). Also used data from Gillette (1909), Gillette & Palmer (1932), Palmer (1952) and MacGillivray (1960). Etymology. The name viburnicola derived from the generic name of host-plant “ Viburnum ” and the ending “- cola ” stand for “inhabitant of”. Gender: feminine. Description. Fundatrix. Body broadly elliptical, sometimes almost round, 1.3–2.4 times as long as its width. Bluish white, due to the entire body, except the terminal segment of the abdomen, being covered with a white powder; without powder from light green to deep green; distal half of antennae (including processus terminalis), two last segments of rostrum, tibiae, tarsi, siphunculi, anal and genital plates and cauda dusky to black; distal halves of middle and hind femora dusky. Cleared specimens with basal halves of tibia almost black, two last segments of the antennae (or the apex of third and last segment in 4-segmented antennae), apices of fore femora, distal halves of middle and hind femora, distal halves of tibia, tarsi and siphunculi dark brown, antennae (except for the last two segments), last two segments of rostrum, sclerites and bands on tergites of the abdomen and peritremes, the subgenital and anal plates and cauda brown, head, coxae, trochanters, basal halves of fore and bases of middle and hind femora light brown. Dorsal surface of thorax and abdomen almost not sclerotized, sclerotized only rare small sclerites on abdominal tergites I–VII, band on tergite VIII, small marginal sclerites on segments I–VII and peritremes; sclerites on tergite VII sometimes grouped together in strongly interrupted band. Surface of dorsal side of head smooth, of ventral side of head with sparse pointed spinules; on dorsal side of thorax and abdominal tergites I–VI smooth, on marginal sclerites on abdominal segment VII with rows of large pointed spines; on tergite VII with rows of small pointed spinules which on tergite VIII partially fused and forming short scales; surface of ventral side of thorax smooth, of abdomen with long rows of small pointed spinules sometimes forming strongly stretched cells. Marginal tubercles always present on pro-, meso- and metathorax and on abdominal segments II–IV, tubercles are absent on other body segments; total number of marginal tubercles on whole body—8–12. Spinal tubercles sometimes present on abdominal tergite VII. Setae on the whole body and appendages are finely pointed, except tibia, where some of setae pointed, but not finely pointed. Chaetotaxy of first tarsal segments 3,3,3. Head with weak traces of epicranial coronal suture or without such traces. Antennae 5-segmented or rarely 4-segmented as a result of fusing of 3rd and 4th segments or 3rd, 4th and 5th segments; antennae without secondary rhinaria. Rostrum reaching mesothorax; ultimate rostral segment short wedge-shaped with slightly concave edges. Legs shortened. Spiracles rounded reniform. Peritremes on abdominal sternites I and II separated by a distance more than diameter of peritreme. Siphunculi without setae. Cauda elongated escutcheon-shaped. Hind tibiae not noticeably swollen and with 7–17 pheromone plates on apices. Alatae viviparous female (emigrant). Body egg-shaped, 1.8–2.3 times as long as its width. Head and thorax black, abdomen pale greenish yellow with dusky to blackish green lateral areas and dorsal bands; antennae, legs (except proximal ends of femora), rostrum, siphunculi, and anal and genital plates dusky to black; cauda pale to dusky. Cleared specimens with head, thorax, antennae (except processus terminalis of last antennal segment), distal halves of fore femora, middle and hind femora (except base), bases and apices of tibia (less often the whole tibia), tarsi and siphunculi dark brown; two last segment of rostrum, middle parts of tibiae, sclerites and bands on tergites and sternites of abdomen, marginal sclerites and peritremes on abdominal segments I–VII and subgenital and anal plates brown; processus terminalis, coxae, trochanters, basal halves of fore femora, base of middle and hind femora and cauda light-brown. Abdominal dorsum with sclerotized bands on all tergites and large marginal sclerites on segments I–VII; band on tergite I thin, sometimes divided into large separate sclerites; bands on tergites II–VII and marginal sclerites on segments V–VII fused in a sclerotized shield on which sometimes present a membranous area on the boundary between tergites; band on tergite II fused with sclerotized shield anterolaterally with a membranous area on the boundary between tergites II and III. Ventral side of abdomen with paired sclerotized maculae located along margins of sternites II–VI. Surface of dorsal side of head smooth, of ventral side of head with sparse pointed spinules; on the pronotum with large pointed spines, sometimes sparse, and sometimes located more or less along the contour of the cell; on the mesonotum and metanotum and on the ventral side of the thorax smooth; on abdominal tergites I–VI with large pointed spines, rare on the anterior tergites and more frequent on the posterior ones, where they form a more or less distinct cellular structure; on tergite VII cells begin to disintegrate, spines slightly smoothed out and forming short rows and on tergite VIII spines partially fused and forming short scales; marginal sclerites on tergites I–VII with rows of large pointed spines forming cellular structure; surface of ventral side of abdomen with long rows of small pointed spinules sometimes forming strongly stretched reticulate cells and spinules are expressed more clearly on sclerotized areas. Marginal tubercles always present on prothorax and abdominal segments I–IV; total number of marginal tubercles on whole body—8–10; they protuberant up to semicircular or papilliform, diameter of tubercles 1.1–2.6 times as long as high. Spinal tubercles always present on abdominal tergite VII and very rare also on tergite VI. Setae on the antennae, dorsal side of head, thorax, legs and on abdominal tergites I–V pointed or finely pointed, on abdominal tergites VI–VIII, on ventral side of head and body, rostrum, subgenital and anal plates and cauda finely pointed. Chaetotaxy of first tarsal segments 4,4,4, only rarely on one leg first tarsal segments with 3 or 5 setae. Head with or without weak traces of epicranial coronal suture, frontal tubercles are low, but distinct, median tubercle not reaching the level of antennal tubercles. Antennae 6-segmented and only small part of individual have one 5-segmented antenna as a result of fusing of 3rd and 4th segments; 3rd antennal
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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 | 0.000 |
| Open science | 0.000 | 0.001 |
| Research integrity | 0.000 | 0.000 |
| Insufficient payload (model declined to judge) | 0.009 | 0.001 |
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".