Dictyogenus muranyii Vincon, Launay, Le Doare, Ruffoni & Reding 2019, sp. n.
Bibliographic record
Abstract
Dictyogenus muranyii Vinçon, Launay, Le Doaré, Ruffoni & Reding, sp. n. http://lsid.speciesfile.org/urn:lsid: Plecoptera.speciesfile.org: TaxonName:506376 (Figs. 27–51) Dictyogenus fontium – Despax, R. (1940). Bulletin de la Société d’Histoire Naturelle de Toulouse, 75:296. Dictyogenus fontium – Vinçon, G. (1996). Bulletin de la Société Entomologique Suisse, 69:72. Dictyogenus fontium gr sp 3-GV sensu Gilles Vinçon (early-release DNA sequence on: www.boldsystems.org, unpublished) Materials examined. Holotype male: FRANCE, Vercors Massif, Isère department (38), Karstic Spring of Bruyant river, above Engins, Lans-en- Vercors (38250), 45° 8.798123'N, 5° 37.049358'E, 982m a.s.l., 09.06.2017, leg. G. Vinçon, deposited in the MZL (catalogue number: GBIFCH00652534). Paratypes: same locality, same date, 3♂, 1♀, leg. G. Vinçon, deposited in the MZL (catalogue number: GBIFCH00652525, GBIFCH00652519); same locality, same date, 3L, leg. J.-P.G. Reding, deposited in the MZL (catalogue number: GBIFCH00652514). Additional specimens. We examined many other specimens. These are stored in the collections of Bertrand Launay (BLC), Gilles Vinçon (GVC), Jean-Paul G. Reding (RC), Dávid Murányi (MC), Jacques Le Doaré (JLDC), Alexandre Ruffoni (ARC) and MZL. FRANCE Vercors Massif Drôme department (26): Archiane torrent, Drôme tributary, NE Châtillon-en-Diois, Menée, Cirque d’Archiane, 44° 44.770828'N, 5° 30.214097'E, 760m, 31.07.1990, 1♂; 16.09.1990, 2♀ (leg. G. Vinçon; GVC). Spring at Brudour cave, Brudour River, Bourne tributary, Bouvante (26190), 44° 55.67493'N, 5° 19.257459'E, 1182m, 13.04.2016, 3L; 02.06.2016, 2♂, 2♀, 1L, 7E (leg. B. Launay; BLC; used for molecular studies by IRSTEA, numbers B079 and B080); 21.05.2017, 1E (leg. G. Vinçon; GVC); 09.06.2017, 9E (leg. J.-P.G. Reding; RC). Adouin river, near its spring, Vernaison and Bourne tributary, Tourtre, Saint-Martin-en- Vercors (26420), 45° 0.120928'N, 5° 27.550379'E, 793m, 21.05.2017, 1♂, 1♀ (leg. G. Vinçon, GVC); 09.06.2017, 11♀, 1E (leg. G. Vinçon; RC; 1♀ used for molecular studies by SwissBOL, MZL, catalogue number GBIFCH00280854); 2♂, 17♀ (leg. G. Vinçon; GVC). Cholet river, Lyonne and Bourne tributary, Combe Laval, Saint-Laurent-en-Royans (26190), 44° 59.859883'N, 5° 20.75296'E, 355m, 21.05.2017, 2♂, 6E (leg. G. Vinçon; GVC). Isère department (38): Bruyant river, Furon and Isère tributary, above Engins, Lans-en-Vercors (38250), 45° 8.798123'N, 5° 37.049358'E, 982m, 06.10.1991, 1E; 25.06.1995, 7♂, 4♀; 10.05.1998, 1♂; 10.06.2007, 1♂; 22.06.2008, 1♂; 22.06.2009, 32♂, 6♀ (1♂ used for molecular studies by A. Reding); 07.07.2012, 7♂, 2♀, 1L (leg. G. Vinçon; GVC); 07.06.2015, 3♂, 2♀, 6L, 5E (leg. B. Launay; BLC); 09.06.2017, 2♂, 1♀, 17E (leg. G. Vinçon; GVC); 7♂, 1♀, 7L, 3E (leg. J.-P.G. Reding; RC; 1♂ used for molecular studies by SwissBOL, MZL, catalogue number GBIFCH00280811). Cuves de Sassenage strong rheocrene spring, Germe brook, Furon and Isère tributary, Sassenage (38474), 45° 12.516243'N, 5° 39.078175'E, 330m, 15.06.1991, 1♂, 2♀ strongly brachypterous (leg. G. Vinçon; MC). Drevenne river, Isère tributary, Pont Chabert, Saint-Gervais (38470), 45° 10.643943'N, 5° 29.885486'E, 885m, 15.06.1991, 1L (leg. G. Vinçon; GVC); 31.05.2012, 2♂; 17.07.2012, 2L; 11.07.2015, 3L (leg. J. Le Doaré; JLDC); 06.06.2015, 1E (leg. B. Launay; BLC). Font Noire river, Bourne tributary, Villard-de- Lans (38250), 45° 4.472474'N, 5° 33.970966'E, 1010m, 01.06.2016, 1♂, 1E (leg. B. Launay; BLC; used for molecular studies by IRSTEA, number B120). Fauge river, Bourne tributary, Villard-de-Lans (38250), 45° 3.373805'N, 5° 34.664105'E, 1230m, 01.06.2016, 1E (leg. B. Launay; BLC). Spring of Furon river, Lans-en-Vercors (38250), 45° 6.304551'N, 5° 36.221224'E, 1294m, 12.07.2015, 6L (leg. J. Le Doaré; JLDC). Chartreuse Massif Isère (38) and Savoie (73) departments: Sarcenas river at Sarcenas, Isère tributary, (38700), 45° 16.829887'N, 5° 45.251584'E, 1093m, 20.04.1986, 5L; 01.06.1986, 4L; 05.10.1986, 1♂ (leg. G. Vinçon; GVC). Spring of Guiers-Vif river, Rhône tributary, Cirque de Saint-Même, Saint-Pierre-D’Entremont (73670), 45° 23.491629'N, 5° 53.464859'E, 1050m, 21.06.1992, 3♀; 12.09.1992, 4♀, 1E; 21.06.1992, 3♀ (leg. G. Vinçon; GVC). Karstic spring of Guiers Mort, Rhône tributary, Saint-Pierre-de-Chartreuse (38380), 45° 19.571976'N, 5° 51.452039'E, 1360m, 11.09.1938, stage and numbers not specified (leg. Ms. Daudin, fide Despax 1940). Diagnosis. General color dark brown with tawny and yellow spots (Figs. 27, 28). Males and females macropterous; only two females were found strongly brachypterous. Apex of the frontal sclerite of the epiproct of adult males very slightly turned downwards, in lateral view (Fig. 33). Female subgenital plate covering half of the abdominal sternum 9 (Fig. 36). Body length of males 17.2 to 20.9 mm; females 18 to 23.6 mm. Anterior wings of males 15 to 19.3 mm; females 17.7 to 21.5 mm. Posterior wings of males 12.5 to 15.8 mm; females 15.3 to 17.4 mm. Adults (Figs. 27–36). Upper side of the head brown, with large yellow spots (Fig. 28). M-line yellow, not interrupted in its middle (Fig. 28). Between the lateral ocelli, a large, ovoid, yellow area delimitated posteriorly by the epicranial suture (Fig. 28). Presence of a large, yellow, median band extending from the anterior margin of the pronotum to its posterior margin (Fig. 28). Band slightly constricted in the middle and then steadily widening toward the posterior margin (Fig. 28). A tawny area on each side of the pronotum, with dark, sculpted rugosities (Fig. 28). Anterior and posterior angles of pronotum almost rectangular (Fig. 28). Abdominal sterna 1 to 6 pale yellow, with two dark patches. Antennae dark brown; cerci light brown with basal part pale yellow (Figs. 29, 30). Wing venation as typical for the genus (Fig. 31; cf. Fig. 8). Forewing with the two cross-veins “ra- rp” and “rp- ma” nearly aligned (like in Fig. 8). Numerous crossveins forming a reticulated area between RA and RP (Fig. 31; cf. Fig. 8). Cross-vein “ra- rp” and subcostal area faintly infuscate (as in Fig. 8). Male terminalia (Figs. 29, 30, 32–35). Epiproct flanked by flat and spatulate lateral stylets (Figs. 33, 34). Abdominal tergum 10 divided into hemiterga whose lobes are covered with a bunch of 20 to 25 long setae in which 3 to 6 stronger and longer spines (half of the length of the hemitergal lobes) are embedded (Figs. 29, 32). Hemitergal lobes bulb-shaped with a slight distal knob (Fig. 30), both pointing rearwards (Fig. 30) and almost horizontally toward each other (Figs. 29, 32). Apex of frontal sclerite of epiproct slightly turned downwards, in lateral view (Fig. 33). Lateral stylets long, only slightly enlarged at apex, in lateral view (Figs. 33, 34). Abdominal sternum 7 composed of multiple plates (as in Figs. 7, 59, 82). Females (Fig. 36). Females not formally identifiable to species level. Female subgenital plate (Fig. 36) covering at most half of sternum 9. Its general shape is semi-circular with a shallow Vshaped median notch. Mature larvae (Figs. 37–45). Interocellar area with a narrow yellow patch nearly reaching lateral ocelli (Figs. 37–39). Lateral ocelli with small lateral circum-ocellar yellow patch (Fig. 38). A large, elliptical yellow patch above each lateral ocellus (Figs. 37–39). M-line well visible only in its medial, crescent-shaped, section (Figs. 37–39). Pronotum wider than long (Figs. 38, 39). Medio-dorsal setae on pronotum long, but not compacted, sometimes covering only the posterior half of the pronotum (Figs. 40, 41). Medio-dorsal row of setae present on mesonotum and metanotum (Fig. 40). Abdominal terga with a row of short and sparse medio-dorsal setae (Fig. 42). Paragenital plates, in ventral view, without spines, or with only 1 spine on one of the paragenital plates, but with numerous empty spine insertion points (Fig. 44). Medio-dorsal row of swimming-hairs of caudal setae sparse, slightly longer than the diameter of the cerci (Fig. 43). General aspect as in Fig. 37. Egg characteristics (Figs. 46–51). General shape triangular or trilateral in cross section. Posterior pole of egg regularly rounded; ridges protruding (Figs. 46, 47). Chorionic surface spring of Brudour, Drôme dpt, France. Photo B. Launay. 43. Medio-dorsal setae on cerci. Karstic spring of Brudour, Drôme dpt, France. Photo A. Ruffoni. 44. Paragenital plates, ventral view. Karstic spring of Brudour, Drôme dpt, France. Photo B. Launay. 45. Stipe. Karstic spring of Brudour, Drôme dpt, France. Photo B. Launay. with polygonal follicle cell impressions (Figs. 48, 50, 51). Anchor papillate, donut shaped apically with central depression (Figs. 48, 49). Micropyles not protruding and arranged regularly in a line in the middle of the egg (Figs. 47, 50). Eclosion line absent (Figs. 46, 47). Comparison to Congeners. Adults. In the adult male of Dictyogenus muranyii sp. n., a wide, V-shaped membranous area between the hemitergal lobe and the inner anterior corner of the hemitergum is present (Figs. 29, 32), whereas this area is sclerotized and much narrower in D. alpinum (Fig. 56). The lateral stylets in D. muranyii sp. n. are slightly enlarged apically (Figs. 33, 34), intermediate in form between those of D. alpinum (Fig. 57) and those of the D. fontium species complex (Fig. 80). In th
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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) | 0.001 | 0.000 |
| Meta-epidemiology (broad) | 0.000 | 0.000 |
| Bibliometrics | 0.002 | 0.001 |
| Science and technology studies | 0.001 | 0.001 |
| Scholarly communication | 0.000 | 0.001 |
| Open science | 0.001 | 0.001 |
| Research integrity | 0.001 | 0.001 |
| Insufficient payload (model declined to judge) | 0.028 | 0.012 |
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".