Bibliographic record
Abstract
Acicnemis kiotoensis Nakane, 1963 Figs 2 C, 3 B, 4 A, 6 F 1–6, 2, 16 Type material examined (Japan: 73; Taiwan: 4; Total: 77). Holotype. Japan: Kyoto Prefecture: • Kurama, 17. VI. 1954, T. Nakane, bears red label reading “ HOLOTYPE ”, bears pink label reading “ 185-5 ”, Syst. Ent. Hokkaido Univ Japan SEHU 0000005125, HUM. Paratype. Japan: Kagoshima Prefecture: • Yakushima Island, Miyanoura, 28. IV. 1954, Y. Kurosawa, bears red label reading “ PARATYPE ” (1, HUM). Non-type material. Japan: Kagoshima Prefecture: • Kirishima, 18. IX. 2007, J. Aoki (2, KUM), JHL_AREV_161, JHL_AREV_162; • Mt. Kirishima, 22. VII. 1956, J. Nagao, (1, KUM), JHL_AREV_775; • Amami Oshima, Hatsuno, 25. V. 1960, T. Shibata (1, KUM), JHL_AREV_177; • Chuorindo, Amami Oshima, 27. VI. 1980, A. Izumi (1, LBM), LBM 5117; • Chuorindo, Amami Oshima, 30. VI. 1980, Yoshikawa (1, LBM), LBM 5119; • Hatsuno, Amami Oshima, 1–8. VII. 1973, M. Ito (1, LBM), LBM 5130; • Yuwan, Amami Oshima, 7. VIII. 1964, M. Nagai (1, HUM), JHL_AREV_645; • Amami Oshima, 21. VII. 1955, T. Shirozu (1, KUM), JHL_AREV_660; • Ishihara-rindo, Amami Oshima, 9–11. VI. 1978, R. Noda (1, KUM), JHL_AREV_661; • Nonigawa, Amami Oshima, 17. VI. 1963, J. Nagao (1, KUM), JHL_AREV_662; • Hatsuno, Amami Oshima, 27. V. 1960, T. Shibata (1, ZMH), ZMH 837205; • Yudomari-rindo, Yakushima Island, 26. VII. 1982, A. Seki (2, LBM), LBM 5120, 5121; • Miyanoura, Yakushima Island, 17. VII. 1968, H. Nomura (1, LBM), LBM 5124; • Miyanoura, Yakushima Island, 21–22. VII. 1974, K. Emoto (2, LBM), LBM 5126, 5127; • Miyanoura, Yakushima Island, 15–26. VII. 1972, H. Huzita (2, LBM), LBM 5129, 5131; • Miyanoura, Yakushima Island, 26–29. VII. 1974, T. Mikage (5, KUM), JHL_AREV_648 – JHL_AREV_650; • Miyanoura, Yakushima Island, 29. VIII. 1952, Takeya & Hirashima (1, KUM), JHL_AREV_653; • Miyanoura, Yakushima Island, 18. VI. 1975, Y. Kurosawa (1, NMNS), JHL_AREV_679; • Okawa-rindo, Yakushima Island, 1–2. VIII. 1974, T. Mikage (2, KUM), JHL_AREV_646, JHL_AREV_647; • Okawa, Yakushima Island, 22. VII. 1975, H. Akiyama (1 dissected male, NMNS), JHL_AREV_157; • Shiratani, Yakushima Island, 26–30. VII. 1979, M. Miura (8, HUM), JHL_AREV_634 – JHL_AREV_641; • Shiratani, Yakushima Island, 24–25. VII. 1974, T. Mikage (5, KUM), JHL_AREV_657 – JHL_AREV_659; • Kosugidani, Yakushima Island, 19. VII. 1974, T. Mikage (1, KUM), JHL_AREV_656; • Kosugidani, Yakushima Island, 23. VII. 1950, T. Shirozu (1, KUM), JHL_AREV_655; • Kosugidani, Yakushima Island, 9. – 10. VII. 1952, Y. Kurosawa (4, NMNS), NSMT-I-C 10267 –10269, NSMT-I-C 10301; • Hanayama Natural Forest, Yakushima Island, 21. VIII. 1983, Sk. Yamane (3, HUM), JHL_AREV_642 – JHL_AREV_644; • Mt. Hoyoshi, Minamiosumi-cho, 24–25. III. 2018, R. Ito (1, KUM), JHL_AREV_840; • Mt. Yuwan, Amami-Oshima, 30. VII. 1963, L. Gressitt (1 dissected male, KUM), JHL_SYN_152; Kyoto Prefecture: • Mt. Kurama, 30. V. 1982, K. Masaki (1, LBM), LBM 5118; • same locality, 8. X. 1978, K. Masaki (1, LBM), LBM 5122; Miyazaki Prefecture: • Miyakonojo-shi, Natsu-cho, Miike, 22. VI. 2019, R. Ito (1, KUM), JHL_AREV_175; • Mt. Aoidake, 7. VIII. 1974, K. Morimoto (1 dissected male, KUM), JHL_DNA_147; Nagasaki Prefecture: • Mt. Taterasan, Izuhara, Tsushima Island, 24–27. VII. 1985, A. Saito (15, CMIC), CBM–ZI 68476 –68490; • Mt. Tatera, Tsushima Island, 18–20. V. 1961, H. Kamiya (2, KUM), JHL_AREV_651, JHL_AREV_652; Nara Prefecture: • Kasugayama, 25. VII. 1981, K. Masaki (1, LBM), LBM 5116; • Kasugayama, 10. V. 1964, K. Kinugasa (1, LBM), LBM 5133; • Kasugayama, 20. V. 1951, K. Sawada (1, KUM), JHL_AREV_654; • Mt. Kasuga, 9. V. 1952, K. Sawada (1 dissected male, KUM), JHL_SYN_153; Okinawa Prefecture: • Okinawa Island, Yonahadake, 8–29. VI. 1977, H. Irie (2, KUM), JHL_AREV_172, JHL_AREV_173; • Iriomote Island, Shirahama, 23–24. VI. 1970, H. Makihara (2, KUM), JHL_AREV_158, JHL_AREV_159; • same locality, 31. VIII – 5. IX. 1969, H. Makihara (6, KUM), JHL_AREV_163 – JHL_AREV_168; • same locality, 26. VII. 1963, Y. Miyatake (1, KUM), JHL_AREV_169; • Okinawa Island, Yona, 9–13. VIII. 1969, H. Makihara (1, KUM), JHL_AREV_176; • Iriomote Island, Nakara River, 25–28. VI. 1970, H. Makihara (2, KUM), JHL_AREV_170, JHL_AREV_171; • Iriomote Island, Taketomi-cho, Mt. Tedo, 2. X. 2017, K. Narita (1, KUM), JHL_AREV_174; • Iriomote Island, 28. VI. 1978, M. Kinjo (1, RUMC), JHL_AREV_524; • Iriomote Island, Funaura, 8. X. 1977, M. Arasaki (1, RUMC), JHL_AREV_525. Taiwan • Mt. Hsin Kao, 1. VII. 1961, S. Ueno, JHL_AREV_160 (1, KUM); • Meifeng, 15. V. 1983, H. Townes (1, CMNC), JHL_AREV_667; • Anmashan, Taichung Hsien, 11–15. V. 1992, A. Smetana (2, CMNC), JHL_AREV_707, JHL_AREV_708. Diagnosis. Body length 4.5–7.0 mm. Covered in pale and dark brown scales, with two obliquely shaped pale brownish, black-bordered spots across middle of elytra. Second funicular antennomere longer than funicular antennomeres 3 + 4 (Fig. 2 C) (compare with A. koguma, which has the second funicular antennomere shorter than funicular antennomeres 3 + 4). Pronotum lacking impunctate longitudinal midline (present in A. koguma). Scutellum diagnostic: large, shiny, and lacking scales (Fig. 3 B). Odd and 2 nd elytral intervals with erect scales (scales beginning at middle of elytra on 2 nd interval; from elytral base on odd intervals). Sclerolepidia indistinct, forming low, rounded, non-protruding tubercles (Fig. 4 A). Third tarsomeres emarginate (not truncate as in A. koguma). Pedon with lateral edges approx. parallel in dorsal view but converging evenly into a wide, blunt point. Internal sac not visible inside the aedeagus, but with a non-hooked protruding structure (unmodified in posterior 1 / 2, with roughened in anterior 1 / 2) that is clearly longer than the pedon (Fig. 6 F 1 – 2). Distribution. This distinctive species occurs in Japan (mainland, throughout the Ryukyu Islands) and Taiwan.
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 | 0.001 |
| Science and technology studies | 0.002 | 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) | 0.007 | 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".