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Record W6949898795 · doi:10.5281/zenodo.4526121

Amblyseius andersoni

2020· article· en· W6949898795 on OpenAlex

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aboutThe title or abstract carries a Canadian signal from the geographic lexicon.
no affNo Canadian affiliation: this work is invisible to an affiliation-only frame.
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Bibliographic record

VenueZenodo (CERN European Organization for Nuclear Research) · 2020
Typearticle
Languageen
FieldAgricultural and Biological Sciences
TopicFungal Plant Pathogen Control
Canadian institutionsnot available
Fundersnot available
KeywordsAmblyseiusSetaPhytoseiidaeArthropod mouthpartsHolotypeParasitiformes

Abstract

fetched live from OpenAlex

Amblyseius andersoni (Chant) Typhlodromus andersoni Chant 1957: 296. Typhlodromus (Amblyseius) andersoni, Chant 1959: 92. Amblyseius (Amblyseius) andersoni, Muma 1961: 287. Typhlodromus (Typhlodromus) andersoni, Westerboer & Bernhard 1963: 682-689. Amblyseius (Multiseius) andersoni, Denmark & Muma 1989: 84. Amblyseius andersoni, Athias-Henriot 1958 b: 33; Moraes et al. 2004: 14; Chant & McMurtry 2004a: 199; 2007: 75. Amblyseiopsis potentillae Garman 1958: 7 (synonymy according to Chant & Yoshida-Shaul 1990). Amblyseius charui Gupta (synonymy according to Gupta 1985). Amblyseius reflexus Knisley & Denmark 1978: 8-10 (synonymy according to Chant & Yoshida-Shaul 1990). Typhlodromus (Amblyseius) britannicus Chant 1959: 87-88 (synonymy according to Chant & Yoshida-Shaul 1990). This species belongs to the obtusus species group with presence of setae J2 and Z1, seta Sources of measurements – Ukraine: Kolodochka & Bodarenko (1993); -: not provided. Sources of measurements for ♀♀ & ♂♂ – China (cited as Amblyseius magnus Wu, junior synonym of T. volgini according to Ryu & Ehara 1991): Wu (1987); Russia: Wainstein & Beglyarov (1971); South Korea: Ryu & Ehara (1991); -: not provided. Z4 short not as long as 2/3 between its base and that of seta s4, female ventrianal shield not vase-shaped/divided into separate ventral and anal shield and not wider at the level of anus than at the level of setae ZV2. It belongs to the andersoni species subgroup of this species group having calyx cup-shaped. This species is distributed worldwide but is mainly reported from Europe. It has been observed on cultivated plants in orchards (apple, peach, pear and citrus) and vineyards, particularly in humid areas (Chant & Hansell 1971; Papadoulis & Emmanouel 1991; Ivancich-Gambaro 1994; Papaioannou-Souliotis et al. 1994; Nicotina 1996; Duso & Pasini 2003; Ragusa 2006). Several studies focused on the biology of A. andersoni and on its ability to feed on plant pests. It is reported to feed on P. ulmi, Frankliniella occidentalis (Pergande) and Aculops lycopersici (Massee) (Koveos & Broufas 2000; Fischer and Mourrut-Salesse 2005; Houten et al. 2005; Lorenzon et al. 2012). This species was already known from Slovenia. With 204 specimens collected in total (see above) in 23 locations, it was one of the most abundant and more widespread species reported in this survey. It has been observed in various locations, probably because of the high relative humidity in these regions. Amblyseius andersoni was already mentioned from the Slovenian fauna (Miklavc 2006; Bohinc and Trdan 2013; Bohinc et al. 2018). World distribution: Algeria, Austria, Azerbaijan, Canada, Cyprus, Czechoslovakia, Czech Republic, Denmark, England, France, Georgia, Germany, Greece, Hungary, Italy, Japan, Latvia, Moldova, Morocco, Netherlands, Poland, Portugal, Serbia, Slovakia, Slovenia, Spain, Sweden, Switzerland, Syria, Turkey, Ukraine, USA. Specimens examined: 135 ♀♀, 33 ♂♂ and 36 immatures in total. Straža pri Raki (aasl 240 m, lat. 45°55’28”N, long. 15°24’26”E), 3 ♀♀ on Acer pseudoplatanus L. (Aceraceae), 1 immature on Capsicum annuum L. (Solanaceae), 2 ♀♀ on Vitis vinifera L. (Vitaceae), 21 ♀♀ and 5 ♂♂ on Cucumis sativus L. (Cucurbitaceae) and 1 immature on Diospyros kaki Thunberg (Ebenaceae), 19/ VI /2018; Ravni (aasl 300 m, lat. 45°56’44”N, long. 15°24’21”E), 1 ♀ on Prunus cerasus L. (Rosaceae), 19/VI/2018; Arnovo Selo (aasl 192 m, lat. 47°58’07”N, long. 15°33’49”E), 7 ♀♀, 1 ♂, and 2 immatures on Malus domestica Miller (Rosaceae), 1 ♀ on Rubus fruticosus L. and 2 ♀♀ on P. cerasus, and 14 ♀♀, 1 ♂ and 2 immatures on Tilia cordata Miller (Malvaceae), 19/VI/2018; Ljubljana, Hotel Azur (aasl 296 m, 46°02’42”N, 14°28’25”E), 1 ♀ on M. domestica, 19/VI/2018 and 8 ♀♀ and 1 immature on Bambusa vulgaris Schrader (Poaceae), 21/VI/2018; Bukovica (aasl 49 m, lat. 45°54’06”N, long. 13°39’30”E), 11 ♀♀, 5 ♂♂ and 3 immatures on P. cerasus and 1 ♀ on Ficus carica L. (Moraceae), 20/VI/2018; Bilje (aasl 72 m, lat. 45°53’60”N, long. 13°38’41”E), 2 ♀♀ on V. vinifera, 20/VI/2018; Prvačina (aasl 47 m, lat. 45°53’22”N, long. 13°42’54”E), 2 ♀♀ on Prunus persica L. (Rosaceae), 1 ♀ and 1 immature on M. domestica, and 4 ♀♀, 1 ♂ and 2 immatures on Prunus pumila L. (Rosaceae), 20/VI/2018; Izola-Pivol (aasl 30 m, lat. 45°32’27”N, long. 13°40’51”E), 1 ♀ and 1 immature on Pyrus communis L. (Rosaceae) and 1 ♂ on Juglans regia L. (Juglandacae), 21/ VI /2018; Parecag (aasl 72 m, lat. 45°28’44”N, long. 13°37’49”E), 1 ♀ on Prunus domestica L. (Rosaceae), 21/VI/2018; Maribor, Plant Protection Institute (aasl 267 m, lat. 46°34’07”N, long. 15°38’12”E), 4 ♀♀ on M. domestica and 4 ♀♀, 2 ♂♂ and 2 immatures on P. persica, and 2 ♀♀ on V. vinifera, 22/VI/2018; Bukovska vas (aasl 370 m, lat. 46°32’57”N, long. 15°03’01”E), 1 ♀ and 1 ♂ on Fragaria sp. (Rosaceae), 12/VII/2018; Škofljica, Gumnišče 15 (aasl 305 m, lat. 45°58’15”N, long. 14°34’17”E), 1 ♀ and 1 ♂ on Acer campestre L. (Aceraceae), 18/VI/2019; Ljubljana, Biotechnical Faculty (aasl 307 m, 46°02’54”N, 14°28’32”E), 1 ♂ on Cornus mas L. (Cornaceae), 18/VI/2019; Ljubljana, Hotel Katrca (aasl 307 m, 46°3’19”N, 14°20’26”E), 1 ♀ on Carpinus betulus L. (Betulaceae), 18/ VI /2019, and 1 ♀ on Tilia platyphyllos Scopoli (Malvaceae), 22/ VI /2019; Sečovlje, 58a (aasl 3 m, lat. 45°28’43”N, long. 13°37’28”E), 2 ♀♀ on J. regia and on Cornus sanguinea L. (Cornaceae), 19/ VI /2019; Dragonja (aasl 3 m, lat. 45°27’32”N, long. 13°39’04”E), 3 ♀♀ on V. vinifera, 2 ♀♀ and 1 immature on P. pumila, and 1 ♂ on F. carica, 19/ VI /2019; Bertoki (aasl 28 m, lat. 45°32’55”N, long. 13°47’13”E), 1 ♀ on Actinidia deliciosa (A. Chevalier) C.F. Liang & A.R. Ferguson (Actinidiaceae), 19/ VI /2019; Pragersko, Kvedrova ulica (aasl 250 m, 46°23’48”N, 13°40’11”E), 2 ♀♀ and 1 ♂ on Pinus strobus L. and 2 ♀♀ and 1 ♂ on P. sylvestris L. (Pinaceae), 20/ VI /2019; Juršinci, Gabrnik 55 (aasl 301 m, lat. 46°28’43”N, long. 15°58’2”E), 1 ♀ and 1 immature on Rubus tomentosus Borkhausen (Rosaceae), 20/VI/2019; Veržej, Near the football stadium (aasl 182 m, lat. 46°35’27”N, long. 16°10’1”E), 2 ♀♀, 1 ♂ and 1 immature on Ulmus minor Miller (Ulmaceae) and 2 ♀♀ on Quercus robur L. (Fagaceae), 20/VI/2019; Šobec (aasl 418 m, lat. 46°21’22”N, long. 14°9’2”E), 2 ♂♂ and 2 immatures on P. sylvestris, 6 ♀♀, 6 ♂♂ and 4 immatures on Q. robur, 1 ♀ on Picea abies (L.) H. Karsten (Pinaceae), 1 ♀ and 5 immatures on Aesculus hippocastanum L. (Hippocastanaceae), 1 ♀ on Prunus padus L. (Rosaceae), 1 ♀ and 1 ♂ on J. regia and 2 ♀♀ on Fraxinus excelsior L. (Oleaceae), 21/ VI /2019; Kranj (aasl 434 m, 46°16’6”N, 14°20’26”E), 2 ♀♀, 1 ♂ and 3 immatures on P. abies and 4 immatures on Sambucus nigra L. (Adoxaceae), 21/ VI /2019; Spodnje Škofije-Purissima (aasl 50 m, lat. 45°34’21”N, long. 13°46’31”E), 4 ♀♀ and 1 ♂ on Capsicum annuum L. (Solanaceae), 11/VII/2019. Remarks: The description and measurements of the adult females collected agree with those provided by Chant and Yoshida (1990), by Ferragut et al. (2010) for specimens from Spain and by Doker et al. (2019) for specimens from Bosnia-Herzegovina, a close country of Slovenia.

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.

Full frame distilled prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. Learned from the 10,348 direct Codex labels and 10,348 direct Gemma labels. Candidate is the union of thresholded teacher heads; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels or direct frontier model labels.

metaresearch head score (Codex)0.000
metaresearch head score (Gemma)0.000
Version: codex-gemma-dda1882f352aValidation status: machine_predicted_unvalidated
Candidate categoriesInsufficient payload (model declined to judge)
Consensus categoriesInsufficient payload (model declined to judge)
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Not applicable · Consensus signal: none
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.870
Threshold uncertainty score0.992

Codex and Gemma teacher scores by category

CategoryCodexGemma
Metaresearch0.0000.000
Meta-epidemiology (narrow)0.0000.000
Meta-epidemiology (broad)0.0000.000
Bibliometrics0.0000.000
Science and technology studies0.0010.000
Scholarly communication0.0000.000
Open science0.0010.000
Research integrity0.0000.000
Insufficient payload (model declined to judge)0.0160.009

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.

Opus teacher head0.051
GPT teacher head0.204
Teacher spread0.153 · how far apart the two teachers sit on this one work
Validation statusscore_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from it