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Cutoff lows (COLs) are mid-latitude cyclones appear at the upper troposphere. They contain cold air mass derived from the polar region. COLs decrease stability of the lower troposphere (e.g., Hoskins et al. 1985) and often accompany severe weathers (e.g., Mohr et al. 2020), which sometimes causes great damages to mid-latitude regions, such as Japan. Besides, the approaching routes of COLs to the Japan Islands and their seasonal cycles have not been investigated with objective method. In this study, we attempt to elucidate them by utilizing depression detection scheme of Kasuga et al. (2021; K21), which can detect COLs from their early stage (pre-existing trough stage). We have implemented a tracking scheme of COLs by simply searching overlapping of area of COLs. Merge and split of COLs are also recorded to investigate variations of the generation/dissipation of COLs.Generally, COLs approach the Japan Islands from northwest advected by the subpolar jet throughout the seasons. They also approach from southeast in JJA and SON at 200 hPa passing around the North Pacific Subtropical High. These two routes were reported in different studies; we successfully track them with a consistent criterion and confirmed that they have longer durations compared to that of a geopotential minimum detection. Tracks shows different characters at 200 and 500 hPa levels as preceding studies have noted. We have found that strong class of COLs are most frequent in MAM. We are investigating climatological backgrounds of the seasonal variations of COLs and hoping to show the results in the conference., The 28th IUGG General Assembly (IUGG2023) (Berlin 2023)

Camponotus lasiselene Wang & Wu, 1994 (fig. 4) M a t e r i a l s e x a m i n e d. Nepal: Kathmandu, Ranibari Community Forest [27.729444 N 85.3205555 E], 1310 m, pitfall collection, 13– 15.10.2019, 1 ♀ worker (IP Subedi, RP Pokhrel, S Subedi & A Subedi) (CDZMTU); idem, hand collection, 14.04.2021, 2 ♀ workers (IP Subedi, I Pandit & A Subedi) (CDZMTU). D i s t r i b u t i o n. Nepal (new record), China, Thailand, Vietnam. T a x o n o m i c n o t e s. Our worker specimen has an opaque black body with extremely abundant whitish short hairs, brownish red mandibles, antennae and tarsus, square-shaped head, short, broad and dorsally margined alitrunk, pronotum with acute margin, two plier-shaped propodeal spines and large, cylindrical gaster. The specimen was identified as C. lasiselene based on the species description and key in Wang & Wu (1994). C. lasiselene is very close to Fig. 4. Camponotus lasiselene. C. selene in the color, shape and sculpture of the body but has abundant whitish erect hair on the body (Wang & Wu, 1994).

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The aim of this study was to clarify the clinical role of bone single photon emission tomography (SPET) of the lumbar spine in young persons with persistent lumbar pain which might be due to spondylolysis. Thirty-one bone SPET studies were performed on 25 patients (19 males, 6 females) aged 7-26 years (average 15.6 years) who had suffered lumbar pain associated with physical activity, and who were suspected of having spondylolysis. Planar and SPET images of the lumbar spine were obtained 2-3 h following the injection of 99 Tc m -methylene diphosphonate using a single-head rotating gamma camera. The findings on the bone scintigram were compared with those on the radiograph. Bone scintigraphy at presentation was positive in only 7 of 15 sites of the pars interarticularis defects demonstrated on plain radiographs. On the other hand, seven sites of the pars interarticularis which were normal on the radiograph were positive on bone SPET. As clinical symptoms improved after immobilization using a lumbar corset, bone SPET tended to revert towards normal. The planar image was abnormal in only 8 (42%) of the 19 abnormal sites on the SPET image. A bone SPET study is indicated in patients who are negative on radiological tests and who are still suspected of having spondylolysis. If SPET is positive in these patients, the increased bone uptake is most likely suggestive of a state of 'stress reaction', and may be a good indicator for patient management. If negative, further radiological examinations will be required for proper assessment of the origin of lumbar pain.

Dilobocondyla Santschi, 1910 Taxonomy. The genus Dilobocondyla is assigned to the tribe Formicoxenini (Bolton 1994, 2003). A key to the described species was given by Wheeler (1924). Workers of Vietnamese species have the following features. Worker monomorphic; head in full-face view subrectangular; preoccipital carina distinct laterally; posterolateral corner of head with a small acute angle or denticle exterior to preoccipital carina; frontal carina distinct; antennal scrobe shallow but distinct; median portion of clypeus broadly inserted between frontal lobes; anterior clypeal margin weakly convex and with a weak emargination at midpoint; median clypeal seta, if present, indistinct; mandible triangular, with 6 teeth on masticatory margin; antenna 12-segmented, with conspicuous 3-segmented club; eye relatively large; promesonotum in lateral view hardly or weakly raised; promesonotal suture absent dorsally; metanotal groove weakly impressed dorsally; propodeum in lateral view weakly swollen posterodorsad, unarmed; propodeal lobe well developed; femora strongly and abruptly incrassate in distal two thirds; petiole elongate, cylindrical, slightly arcuate in lateral view; subpetiolar process distinct, tooth-like, located anteroventrally near articulation with mesosoma; postpetiole in lateral view with acute anteroventral angle; gaster short, oval in dorsal view. The worker of Dilobocondyla is easily distinguished from that of other myrmicine genera known from Vietnam by posterolateral corner of head with a small acute angle or denticle exterior to preoccipital carina, propodeum unarmed, femora strongly and abruptly incrassate, and petiole elongate and sylindrical. Vietnamese species. One species has been described from Vietnam: fouqueti Santschi (type locality: Ha Noi). Two additional species have been recognized by us from Vietnam: sp. eg-1 (Da Lat); sp. eg-2 (Tay Ye n Tu). Bionomics. We have rarely encountered foraging workers of Dilobocondyla on leaves in undergrowth of natural and man-made forests., Published as part of Eguchi, K., Viet, B. T. & Yamane, S., 2011, Generic synopsis of the Formicidae of Vietnam (Insecta: Hymenoptera), Part I - Myrmicinae and Pseudomyrmicinae., pp. 1-61 in Zootaxa 2878 on page 15

Pheidologeton Mayr, 1862 Taxonomy. The genus Pheidologeton is assigned to the Carebara genus group of the tribe Solenopsidini (Bolton 2003). The genus was preliminarily reviewed by Yamane (2000). Workers of Vietnamese species have the following features. Worker polymorphic; head in full-face view oval or subrectangular in minor, subrectangular or subtrapezoidal with roundly expanded vertexal lobe in media and major; frontal carina and antennal scrobe absent; median portion of clypeus not margined laterally by conspicuous carinae; posteromedian portion of clypeus relatively broadly inserted between frontal lobes; median clypeal seta absent; mandible triangular, 4-6 teeth on masticatory margin (teeth more rounded or worn in major); antenna 11-segmented, with 2-segmented club; eye small to moderate in size, sometimes consisting of only a few ommatidia; mesosoma in lateral view relatively slender in minor, but short and robust in major; promesonotum in lateral view usually well raised as a dome, much higher than anterodorsal border of propodeum; promesonotal suture completely absent dorsally in minor, but often conspicuous in major; posterior slope of promesonotal dome often with a prominence in major; metanotal suture weakly impressed dorsally; propodeal spine always present, but variable in size and shape; propodeum lobe low or almost absent; petiole consisting of anterior peduncle and node (but anterior peduncle ill defined from node in major); gastral shoulder distinct to indistinct. The minor worker of Pheidologeton is similar to the minor of Oligomyrmex (for distinguished characters see under Oligomyrmex) and the worker of Lophomyrmex (see under Lophomyrmex). Vietnamese species. One species has been described from Vietnam: varius Santschi (type locality: Ho Chi Minh City). Four additional species have been recognized by us from Vietnam: diversus (Jerdon) [= sp. eg-3] (Nam Cat Tien, Ninh Thuan, Pu Mat, Quang Tri, Tam Dao); trechideros Zhou et Zheng [= sp. eg-1] (Chua Yen Tu, Pu Mat, Tay Yen Tu, Van Ban); vespillo Wheeler [= sp. eg-2] (Ba Vi, Cuc Phuong, Tay Yen Tu); sp. eg-4 [= cf. affinis (Jerdon)] (Binh Chau-Phuoc Buu, Cuc Phuong, Nam Cat Tien, Pu Mat). Bionomics. Pheidologeton diversus usually inhabits urban areas, bare lands, grasslands, forest edges and sparse forests. In contrast, the other Vietnamese species of Pheidologeton inhabit rather developed forests. Pheidologeton conlonies are extremely large and usually occur in soil under logs and stones. Permanent foraging trails, galleries and tunnels extend outward from the nests. A mass of foragers gather various kinds of food such as living and dead invertebrates, honeydew of homopterans and plant matter (nectar, fruits, seeds, etc)., Published as part of Eguchi, K., Viet, B. T. & Yamane, S., 2011, Generic synopsis of the Formicidae of Vietnam (Insecta: Hymenoptera), Part I - Myrmicinae and Pseudomyrmicinae., pp. 1-61 in Zootaxa 2878 on pages 24-25

Tetramorium Mayr, 1855 Taxonomy. The genus Tetramorium is assigned to the tribe Tetramoriini (for a complete taxonomic history see Bolton 2003). The Oriental species were revised by Bolton (1976, 1977). Workers of Vietnamese species have the following features. Worker monomorphic; head in full-face view subrectangular, with rounded posterior corners; frontal carina usually (but not always) long and distinct; antennal scrobe weak or absent; anteromedian margin of clypeus weakly convex, often with a weak emargination at midpoint, lacking any denticles or teeth; an isolated median seta absent; posteromedian portion of clypeus very broadly inserted between frontal lobes; lateral portion of clypeus modified into a distinct ridge or wall in front of antennal insertion; mandible triangular; masticatory margin with apical and 1 or 2 larger preapical teeth followed by some smaller teeth or minute denticles; palp formula 4,3; antennae 11- or 12-segmented, with 3-segmented club; basal rim of shaft of antennal scape often forming an enlarged lobe expanding ventrad; eye medium to large in size; mesosoma in lateral view weakly convex dorsad; promesonotal suture absent dorsally; metanotal groove absent; anterior part of mesopleuron forming a flange projecting over basal part of fore coxa; propodeal spine present, varying in size and shape; propodeal lobe well developed usually as a triangular lamella or spinose projection but sometimes as a subrectangular or round lamella; petiole pedunculate, with distinct node; a tiny denticle or process present on the anteriormost part of ventral face of peduncle (it is often concealed by mesopleuron and or hind coxa in lateral view); gastral shoulder distinct to absent; apex of sting with a small lamellate appendage; head and mesosoma usually strongly reticulate or rugoso-reticulate. The worker of Tetramorium is similar to those of Rhoptromyrmex and Myrmica (for distingusihing characters see under the latter genera) Vietnamese species. Four species have been described from Vietnam: indosinense Wheeler [= sp. eg-13] (Type locality: Ha Noi; other locality: Ba Vi); infraspinosum Karaviev (type locality: Cau Da); kieti Roncin (type locality: Vietnam); secure Roncin (type locality: Vietnam). An additional 21 species have recognized by us from Vietnam: flavipes Emery [= sp. eg-4; = sp. 39 of SKY: Yamane et al., 2003] (Ba Vi, Chua Yen Tu, Cuc Phuong, Nam Cat Tien, Phu Quoc, Pu Mat, Tay Yen Tu, Van Ban); kheperra (Bolton) [= sp. eg-9] (Ba Vi, Phu Quoc, Tay Ye n T u); lanuginosum Mayr [= sp. eg-17] (Ba Vi, Bac Kan, Tam Dao); nipponense Wheeler [= sp. eg-5] (Ba Be, Ba Vi, Cuc Phuong, Sa Pa, My Yen, Pu Mat, Tay Yen Tu, Van Ban); sp. eg-1 (Sa Pa); sp. eg-2 [= kraepelini Forel: Eguchi et al., 2005] (Ba Vi, Nam Cat Tien, Phu Quoc, Pu Mat, Tay Yen Tu); sp. eg-3 [= sp. 32 of SKY: Eguchi et al., 2005] (Ba Vi, Chua Yen Tu, Tam Dao, Tay Yen Tu, Van Ban); sp. eg-6 [cf. pacificum Mayr] (Sa Pa, Pu Mat); sp. eg-7 (Sa Pa); sp. eg-8 (Ba Be); sp. eg-10 (Tay Yen Tu); sp. eg-12 (Ba Vi, Pu Mat); sp. eg-14 (Binh Chau-Phuoc Buu); sp. eg-15 [= bicarinatum (Nylander): Eguchi et al., 2005] (Tam Dao); sp. eg-16 [= smithi Mayr: Eguchi et al., 2005] (Ba Vi); sp. eg-18 [= walshi (Forel): Yamane et al., 2003] (Cuc Phuong, My Yen, Pu Mat); sp. eg-19 (Ba Be); sp. eg-21 (Cuc Phuong); sp. eg-22 (Nam Cat Tien); sp. eg-23 (Nam Cat Tien, Nui Chua); sp. eg-24 (Nam Cat Tien). Bionomics. Tetramorium species inhabit various habitats such as open lands, grasslands, forest edges and well-developed forests. Their nests are usually found in rotting logs, twigs, wood fragments, under stones and in soil. Workers forage mainly on the ground., Published as part of Eguchi, K., Viet, B. T. & Yamane, S., 2011, Generic synopsis of the Formicidae of Vietnam (Insecta: Hymenoptera), Part I - Myrmicinae and Pseudomyrmicinae., pp. 1-61 in Zootaxa 2878 on page 30