3,429 research outputs found
Acrapex kavumba Bruno Le Ru & Claire Capdevielle-Dulac & Boaz K. Musyoka & Beatrice Pallangyo & Mohamedi Njaku & Onésime Mubenga 2017, sp. nov.
No full texturn:lsid:zoobank.org:act:17B55911-C7C0-4733-B131-D9C0C59FE72A Figs 2C, K, 6A–B Diagnosis Males easily separated from males of other species of the group by the spoon-shaped cucullus and the turn of the hand-shaped vesica being adorned with a large tuft of needle-shaped cornutus (Fig. 2C, K). Etymology Named after the village of Kavumba in Zambia. Type material Holotype ZAMBIA: ♂, Luapula Province, Kavumba, 11°29.074' S, 29°25.757' E, 1193 m a.s.l., 22 Mar. 2012, ex light trap, B. Le Ru leg. (MNHN, gen. prep. LERU Bruno/G161). Paratypes ZAMBIA: 2 ♂♂, North-Western Province, Rwanko Azi, 12°13.212' S, 25°39.064' E, 1413 m a.s.l., 20 Mar. 2012, ex light trap (MNHN, gen. prep. LERU Bruno/G169-G377). TANZANIA: 1 ♂, Iringa region, Sao Hill, 08°27.421' S, 35°10.036' E, 1845 m a.s.l., 22 Jan. 2012, ex larva (in stem of Hyparrhenia sp.), B. Le Ru leg. (MNHN); 3 ♂♂, same locality, Nov. 2015, ex light trap, B. Le Ru leg. (MNHN, gen. prep. LERU Bruno/G937). Description Only the male is known (Fig. 6A–B); antennae cupreous brown dorsally and ochreous ventrally, slightly ciliate; fagellum adorned dorsally with white scales, palpus cupreous brown, adorned with white scales, eyes fuscous. Head and base of thorax brown, thorax becoming gradually ochreous; legs brown-ringed with white; abdomen brown irrorated with fuscous scales, extremity of abdomen densely suffused with buff scales. FORE WING. Ground colour dark ochreous, suffused with fuscous and brown scales, more heavily along veins and in costal area; reniform indicated by few white scales, preceded by some brown scales; longitudinal brown median fascia along lower external margin of cell, ending obliquely at apex; veins below cell adorned with white, fuscous and brown scales; postmedial row of white spots on veins; row of black elongated spots between veins on margin; fringe whitish externally, ochreous suffused with brown internally. Underside of fore wing with ground colour brown, suffused with fuscous scales on costa. HIND WING. Uniformly brown; fringe white suffused with fuscous and adorned with narrow fuscous line. Underside of hind wing brown, suffused with fuscous scales. WINGSPAN. 21–23 mm (4 ♂♂). MALE GENITALIA (Fig. 2C, K). Uncus long, widening in distal third, truncated at apex, tufted with long hairs on upper side. Tegumen with medium-sized rounded penniculi, vinculum pointed, with mediumsized triangular saccus, valves short and broad, cucullus spoon-shaped and tufted with medium size hairs, coastal margin slightly broadened on inner side and produced into narrow, straight, long lobe, roundly pointed; juxta oblong, pear-shaped, with long and wide neck, elongate bifd. Aedeagus short, slightly curved, with two lateral areas adorned with short setae; turn of hand-shaped vesica with large tuft of needle-shaped cornutus. Bionomics One larva was collected at the bottom of a stem of a Hyparrhenia sp. growing in grasslands near marshes (Table 3); like many species of Acrapex, A. kavumba sp. nov. is a markedly hygrophilous species. Unfortunately, no pictures were taken before pupation. All the moths were caught in a light trap in grasslands near marshes. Distribution Tanzania and Zambia. The records are from a mosaic of Zambezian dry evergreen forest and wetter miombo woodland (Mosaic #21) (White 1983) (Fig. 4), belonging to the Zambezian bioregion (Linder et al. 2012) (Fig. 5).Published as part of Bruno Le Ru, Claire Capdevielle-Dulac, Boaz K. Musyoka, Beatrice Pallangyo, Mohamedi Njaku & Onésime Mubenga, 2017, Phylogenetic analysis and systematics of the Acrapex unicolora Hampson species complex (Lepidoptera, Noctuidae, Noctuinae, Apameini), with the description of Fve new species from the Afrotropics, pp. 1-36 in European Journal of Taxonomy 270 on pages 13-16, DOI: 10.5852/ejt.2017.270, http://zenodo.org/record/88948
Acrapex kiakouama Bruno Le Ru & Claire Capdevielle-Dulac & Boaz K. Musyoka & Beatrice Pallangyo & Mohamedi Njaku & Onésime Mubenga 2017, sp. nov.
No full text<p>urn:lsid:zoobank.org:act:5FD4E344-68BA-423B-AF86-347CAD502914</p> <p>Figs 2D, L, 3C, 6C–F</p> Diagnosis <p>Male easily separated from males of other species of the group by the uncus being shovel-shaped at the apex and by the large, plate-like juxta, with a narrow pyriform base and a long and widening, slightly sclerotised neck (Fig. 2D); female easily separated from females of other species of the group by having the antrum strongly sclerotized, with a large, broad ventral plate, bilobate, widening to the front, anterior part shaped like a feshy lip, the posterior part concave (Fig 3C).</p> Etymology <p>Named after Kiakouama, the technician who collected this species in the Republic of the Congo.</p> Type material Holotype <p>REPUBLIC OF THE CONGO: ♂, Kouilou Department, Lac Nanga, 04°56.090' S, 11°56.713' E, 2 m a.s.l., 17 Apr. 2013, ex light trap, B. Le Ru leg. (MNHN, gen. prep. LERU Bruno/G843).</p> Paratypes <p>REPUBLIC OF THE CONGO: 4 ♂♂, same date and locality as holotype, ex light trap, B. Le Ru leg. (MNHN, gen. prep. LERU Bruno/G533-G537-G781); 4 ♀♀, same date and locality as holotype, ex light trap, B. Le Ru leg. (MNHN, gen. prep. LERU Bruno/G536); 1 ♂, Kouilou Province, Lac Loubi, 04°53.573' S, 11°55.535' E, 4 m a.s.l., 16 Apr. 2013, ex light trap, B. Le Ru leg. (MNHN).</p> Description <p>Both sexes look similar; however, the general shape of the female fore wing is more elongated at the apex than in the male and is paler (Fig. 6C–F); antennae bright ochreous dorsally and ochreous ventrally, fliform in female and slightly ciliate in male; fagellum adorned dorsally with grey scales, palpus ochreous grey, eyes fuscous brown. Head and base of thorax bright brown, thorax ochreous; legs ochreous, ringed with grey white; abdomen grey.</p> <p>FORE WING. Ground colour bright ochreous in both sexes, suffused with fuscous and brown scales, more heavily along veins and costal area, particularly in male; reniform indicated by few white scales, surrounded by some brown scales; longitudinal brown median fascia along lower external margin of cell, ending obliquely at apex; veins below cell adorned with white and fuscous scales; row of black elongated spots between veins on margin; fringe grey externally, ochreous suffused with fuscous internally. Underside of fore wing with ground colour ochreous, densely suffused with brown scales.</p> <p>HIND WING. Ground colour pale ochreous in male, more whitish in female; veins slightly irrorated, with fuscous scales, costa and apex more heavily suffused with fuscous scales; hind wing of male much more suffused with fuscous scales than that of female; fringe pale ochreous, suffused with fuscous and adorned with narrow fuscous line. Underside of hind wing pale ochreous in male, more whitish in female, suffused with brown scales but much more heavily on costa and apex; veins slightly irrorated with pale fuscous scales.</p> <p>WINGSPAN. 16–18 mm (4 ♂♂); 20–23 mm (7 ♀♀).</p> <p>MALE GENITALIA (Fig. 2D, K). Uncus long, widening in distal third, shovel-shaped at apex, tufted with long hairs on upper side. Tegumen with medium-sized rounded penniculi, vinculum pointed, with medium-sized triangular saccus, valves short and broad, cucullus rounded and tufted, with medium-sized hairs, coastal margin slightly broadened on the inner side and produced into strong tooth-shaped spine, strongly sclerotized at apex, pointed and curved inwardly; juxta large, plate-like, base pyriform, without sclerotization, with long and widening, slightly sclerotized neck. Aedeagus short, slightly curved, with two lateral areas adorned with short setae; hand-shaped vesica with basal tuft of needle-shaped cornutus, pointed obliquely downward.</p> <p>FEMALE GENITALIA (Fig. 3C). Corpus bursae long and globular, without signa; ductus bursae very short, with strongly sclerotized funnel-shaped connection with ostium; antrum strongly sclerotized, with large, broad ventral plate, bilobate, widening to the front, anterior part shaped like a feshy lip, posterior part concave; dorsal plate small, weakly sclerotized. Ovipositor lobes relatively short (2 times as long as wide), with pointed apex, dorsal surface bearing numerous short and stout setae.</p> Bionomics <p>Biology unknown. The moths were caught in a light trap in grasslands near marshes.</p> Distribution <p> Republic of the Congo. Known from two close localities only in the Kouilou region, south coast of Pointe Noire. Moths were found in a mosaic of lowland rain forest and secondary grassland (Mosaic #11A) (White 1983) (Fig. 4), belonging to the Congolian bioregion (Linder <i>et al</i>. 2012) (Fig. 5).</p>Published as part of <i>Bruno Le Ru, Claire Capdevielle-Dulac, Boaz K. Musyoka, Beatrice Pallangyo, Mohamedi Njaku & Onésime Mubenga, 2017, Phylogenetic analysis and systematics of the Acrapex unicolora Hampson species complex (Lepidoptera, Noctuidae, Noctuinae, Apameini), with the description of Fve new species from the Afrotropics, pp. 1-36 in European Journal of Taxonomy 270</i> on pages 16-17, DOI: 10.5852/ejt.2017.270, <a href="http://zenodo.org/record/889483">http://zenodo.org/record/889483</a>
Acrapex kafula Bruno Le Ru & Claire Capdevielle-Dulac & Boaz K. Musyoka & Beatrice Pallangyo & Mohamedi Njaku & Onésime Mubenga 2017, sp. nov.
No full texturn:lsid:zoobank.org:act:B727D00A-7E31-4B44-9B33-E6DC82D548B2 Figs 1G–J, 2B, J, 3B Diagnosis Male easily separated from males of other species of the group by the shovel-shaped uncus (at the apex) and the distal part of the aedeagus (grooved-shaped), with the vesica having a basal tuft of needleshaped cornutus, pointed downward (Fig. 2B, J). Female easily separated from females of other species of the group by the very short ductus bursae, with a strongly sclerotised funnel-shaped connection with the ostium; antrum sclerotized, with a large, broad ventral plate, slightly bilobate, widening to the front, the anterior part shaped like a thin lip and more sclerotized than the posterior part, slightly concave (Fig. 3B). Etymology Named after the village of Kafulo in Zambia. Type material Holotype ZAMBIA: ♂, Western Province, Kafulo, 14°08.726' S, 23°27.638' E, 1056 m a.s.l., 20 Mar. 2012, ex light trap, B. Le Ru leg. (MNHN, gen. prep. LERU Bruno/G595). Paratypes CAMEROON: 1 ♀, Central Region, Sanaga River, 04°22.387' N, 11°15.162' E, 388 m a.s.l., Dec. 2013, ex light trap (MNHN, gen. prep. LERU Bruno/G603). KENYA: 2 ♂♂, 2 ♀♀, Nyanza Province, edge of Ruma Park, 00°36.293' S, 34°16.046' E, 1221 m a.s.l., 14 Nov. 2012, ex light trap, B. Le Ru leg. (MNHN, gen. prep. LERU Bruno/G511-G513-G529); 1 ♂, Central Province, Ruiru Aukland, 01°05.063' S, 36°55.621' E, 1595 m a.s.l., Jun. 2011 (MNHN). REPUBLIC OF THE CONGO: 1 ♂, Plateau Region, Lefni River, 02°54.501' S, 15°37.776' E, 320 m a.s.l., 13 Apr. 2013, ex light trap (MNHN, gen. prep. LERU Bruno/G584). TANZANIA: 1 ♂, Iringa Region, Lukumburu, 09°40.048' S, 35°16.892' E, 1299 m a.s.l., 17 Apr. 2015, ex light trap, B. Le Ru leg. (MNHN, gen. prep. LERU Bruno/G799). UGANDA: 2 ♂♂, Western Region, Itojo, 00°50.546' N, 30°13.131' E, 1070 m a.s.l., 22 May 2014, ex light trap (MNHN, gen. prep. LERU Bruno/G714). ZAMBIA: 1 ♂, same date and locality as holotype, ex. light trap, B. Le Ru leg. (MNHN, gen. prep. LERU Bruno/G178); 1 ♀, same date and locality as holotype, ex light trap (MNHN, gen. prep. LERU Bruno/G165). Description Both sexes look similar; however, general shape of female fore wing more elongated at apex than in male and fore wings paler in females (Fig. 1G–J); antennae bright fuscous dorsally and ochreous ventrally, fliform in female and slightly ciliate in male; fagellum adorned dorsally with black scales, palpus cupreous brown, eyes fuscous. Head and base of thorax brown, thorax becoming gradually fuscous; legs brown-ringed with buff, buff on inner surface; abdomen fuscous, irrorated with buff scales. FORE WING. Ground colour ochreous in both sexes, suffused with fuscous scales, more heavily along veins and costal area, particularly in males; reniform indicated by a few white scales, preceded by some brown scales; longitudinal brown median fascia along lower external margin of cell, ending obliquely at apex; veins below cell adorned with white, fuscous and brown scales; postmedial row of white spots on veins; row of black elongated spots between veins on margin; fringe whitish externally, fuscous suffused with brown internally. Underside of fore wing with ground colour fuscous, densely suffused with brown scales. HIND WING. Ground colour white, veins slightly irrorated, with fuscous scales, costa and apex more heavily suffused with fuscous scales; hind wing of males much more suffused with fuscous scales than in females; fringe white, suffused with fuscous and adorned with narrow fuscous line. Underside of hind wing white, suffused with fuscous scales but much more heavily on costa and apex; veins slightly irrorated, with fuscous scales. WINGSPAN. 18–22 mm (6 ♂♂); 21–25 mm (5 ♀♀). MALE GENITALIA (Fig. 2B, J). Uncus long, widening in distal third, shovel-shaped at apex, tufted with long hairs on upper side. Tegumen with medium-sized rounded penniculi, vinculum pointed, with mediumsized triangular saccus, valves short and broad, cucullus rounded and tufted with medium-sized hairs, coastal margin slightly broadened on inner side and produced into strong, tooth-shaped spine, strongly sclerotized at apex, pointed and slightly curved inwardly; juxta large, plate-like, without sclerotisation. Aedeagus short, slightly curved, with two lateral areas adorned with short setae; hand-shaped vesica with basal tuft of needle-shaped cornutus, pointed downward. FEMALE GENITALIA (Fig. 3B). Corpus bursae elongated ovoid and globular without signa; ductus bursae very short, with strongly sclerotised, funnel-shaped connection with ostium; antrum sclerotized, with large, broad ventral plate, slightly bilobate, widening to the front, anterior part shaped like a thin lip, more sclerotized than posterior part, slightly concave; dorsal plate small, weakly sclerotized. Ovipositor lobes relatively short (2.2 times as long as wide), with pointed apex, dorsal surface bearing numerous short and stout setae. Bionomics Biology unknown. The moths were caught in a light trap in grasslands near marshes. Distribution Cameroon,Kenya,theRepublicoftheCongo,Tanzania,UgandaandZambia.Mothswerefoundinamosaic of lowland rainforest and secondary grassland (Mosaic #11), in a mosaic of Zambezian dry evergreen forest and wetter miombo woodland (Mosaic #21), in a mosaic of East African evergreen bushland and secondaryAcacia wooded grassland (Mosaic #45) and in undiffentiated montane vegetation (Mosaic #19) (White 1983) (Fig. 4), belonging to the Congolian and Zambezian bioregions (Linder et al. 2012) (Fig. 5).Published as part of Bruno Le Ru, Claire Capdevielle-Dulac, Boaz K. Musyoka, Beatrice Pallangyo, Mohamedi Njaku & Onésime Mubenga, 2017, Phylogenetic analysis and systematics of the Acrapex unicolora Hampson species complex (Lepidoptera, Noctuidae, Noctuinae, Apameini), with the description of Fve new species from the Afrotropics, pp. 1-36 in European Journal of Taxonomy 270 on pages 11-13, DOI: 10.5852/ejt.2017.270, http://zenodo.org/record/88948
Fig. 1 in Phylogenetic analysis and systematics of the Acrapex unicolora Hampson species complex (Lepidoptera, Noctuidae, Noctuinae, Apameini), with the description of Fve new species from the Afrotropics
No full textFig. 1. Adults of species of Acrapex. – A–F. A. cuprescens (Hampson, 1910). A. ♂, upper side. B. ♂, under side. C. ♂, original labels from BMNH. D. ♀, original labels from BMNH. E. Upper side. F. Under side. – G–J. A. kafula le Ru sp. nov. G. ♂, upper side. H. ♂, under side. I. ♀, upper side. J. ♀, under side. Scale bars = 3 mm.Published as part of Bruno Le Ru, Claire Capdevielle-Dulac, Boaz K. Musyoka, Beatrice Pallangyo, Mohamedi Njaku & Onésime Mubenga, 2017, Phylogenetic analysis and systematics of the Acrapex unicolora Hampson species complex (Lepidoptera, Noctuidae, Noctuinae, Apameini), with the description of Fve new species from the Afrotropics, pp. 1-36 in European Journal of Taxonomy 270 on page 8, DOI: 10.5852/ejt.2017.270, http://zenodo.org/record/88948
Sixty Years of Community: St. Olaf Catholic Parish in Eau Claire, Wisconsin, 1952-2012
No full textThis paper will explore how the parish community of St. Olaf in Eau Claire, Wisconsin, established in 1952, reflects the Roman Catholic Church, specifically at the local, state, and national levels in the United States. It will also discuss the various changes that have occurred in the past 60 years of its history in terms of the various locations of worship for the members, the growth of the community outreach programs, and the effects of the Second Vatican Council. This ecumenical council was a meeting of Catholic bishops from around the whole that brought reform to the Catholic Church and affected the relationship of the Catholic Church to the world. The parish at St. Olaf has grown from having only 125 families in 1952 to over 1,000 families in 2012
From Mansions to Towers: A History of Residence Halls at the University of Wisconsin-Eau Claire
No full textThe construction of the University of Wisconsin-Eau Claire's residence halls has generally followed that of the national trend. The school struggled to find enough funds to build residence halls in the early years. Eventually, student housing was in needed so badly that the school had no choice but to provide housing for the students. In 1947, the Dulany mansion was purchased and remodeled by the school. This building served as the University's first resident hall. Since then, eleven resident halls have been built on campus with one more being planned. Life in these residence halls have changed dramatically over time. In the 1960's, the students protested and eventually the strict rules of in loco parentis faded away. After this, students enjoyed the freedoms of new technologies, relaxed rules, and more professional housing leaders. Today, UW-Eau Claire is a thriving university. UW-Eau Claire has been recognized by many as a top school in the Midwest. Much of the success can be attributed to the residence halls and the happiness of the students. My paper will provide UW-Eau Claire and its students with a cohesive history of the residence halls on campus and will also show how student life has evolved since the University was first established
Acrapex malagasy Viette 1967
No full textFigs 2E, M, 6G–I Acrapex malagasy Viette, 1967: 712 –714, fgs 552a–b, 553. Acrapex malagasy – Poole 1989: 20 (catalogue). Diagnosis Easily separated from other species of the group by the large, plate-like juxta, with the base slightly fattened, without sclerotization, with a long and widening neck, ending on each side in a rounded apex, on both sides tufted with small-sized hairs (Fig. 2E). Material examined Holotype MADAGASCAR: ♂, Plateau de l’Imerina, Tananarive, Parc de Tsimbazaza, 1200 m a.s.l., 10 Oct. 1951 (MNHN, gen. prep. 4426). Several specimens are recorded by Viette (1967). Paratype MADAGASCAR: 2 ♂♂, same locality and date as holotype (MNHN); 3 ♂♂, same locality as holotype, 8 Nov. 1954, P. Viette leg. (MNHN, gen. prep. 4438). Description The description of the external features of the holotype by Viette (1967) was accurate (Fig. 6G–H). WINGSPAN. 17–20 mm (♂♂) according to Viette (1967); however, only one specimen is preserved in MNHN. MALE GENITALIA (Fig. 2E, M). (After Viette 1967) Additional description: juxta large, plate-like, base slightly fattened, without sclerotization, with long and widening neck, ending on each side in rounded apex, on both sides tufted with small-sized hairs; aedeagus short, stout, not curved, with two lateral areas adorned with short setae; hand-shaped vesica with tuft of needle-shaped cornutus, pointed obliquely downward. Bionomics Biology unknown. Distribution Madagascar. Only known from the type locality. The record is from secondary grassland replacing upland and montane forest (Mosaic #18) (White 1983) (Fig. 4), belonging to the Sudanian bioregion (Linder et al. 2012) (Fig. 5).Published as part of Bruno Le Ru, Claire Capdevielle-Dulac, Boaz K. Musyoka, Beatrice Pallangyo, Mohamedi Njaku & Onésime Mubenga, 2017, Phylogenetic analysis and systematics of the Acrapex unicolora Hampson species complex (Lepidoptera, Noctuidae, Noctuinae, Apameini), with the description of Fve new species from the Afrotropics, pp. 1-36 in European Journal of Taxonomy 270 on pages 17-18, DOI: 10.5852/ejt.2017.270, http://zenodo.org/record/88948
Claire Tham (1967-)
No full textAs an author, Claire Tham has this far been less concerned to observe the canons of English literature and more concerned to explore its creative possibilities and its adaptability. She also articulates a significant viewpoint about national and personal identity, about cultural tensions in a dynamic urban centre in transition, and about the.flip-side of Singapore’s prodigious prosperity
High Triatoma brasiliensis densities and Trypanosoma cruzi prevalence in domestic and peridomestic habitats in the State of Rio Grande do Norte, Brazil: The source for Chagas disease outbreaks?
No full textA total of 2,431 Triatoma brasiliensis were collected from 39 populations of Paraíba (PB) and Rio Grande do Norte (RN) states, Brazil. In PB, Trypanosoma cruzi infection was not detected in either peridomestic or domestic vector populations. In contrast, in RN, T. brasiliensis was detected with high parasite prevalence in these ecotopes (30.7-40.0%). Moreover, peridomicile insect population densities were more than double the average densities of all other settings evaluated (19.17 versus < 8.94 triatomine/man-hour). Genotyped parasites evidenced a mix of T. cruzi lineages circulating in both peridomestic and sylvatic populations. Although vector control efforts have dramatically decreased Chagas disease transmission to humans, recent outbreaks have been detected in four municipalities of RN state. Our results clearly evidence a worrisome proximity between infected vectors and humans in RN. Indeed, finding of infected T. brasiliensis inside homes is routinely recorded by local vector control surveillance staff around the outbreak area, challenging the current and conventional view that vector transmissions are controlled in northeastern Brazil. This scenario calls for strengthening vector control surveillance and interventions to prevent further Chagas transmission, especially in RN State.Fil: Lilioso, Mauricio. Universidade Federal da Paraíba; BrasilFil: Folly Ramos, Elaine. Universidade Federal da Paraíba; BrasilFil: Rocha, Fabiana Lopes. Universidade Federal da Paraíba; BrasilFil: Rabinovich, Jorge Eduardo. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - La Plata. Centro de Estudios Parasitológicos y de Vectores. Universidad Nacional de La Plata. Facultad de Ciencias Naturales y Museo. Centro de Estudios Parasitológicos y de Vectores; ArgentinaFil: Capdevielle Dulac, Claire. Universite Paris Saclay; FranciaFil: Harry, Myriam. Universite Paris Saclay; FranciaFil: Marcet, Paula Lorena. Centers for Disease Control and Prevention; Estados Unidos. Consejo Nacional de Investigaciones Científicas y Técnicas; ArgentinaFil: Costa, Jane. Fundación Oswaldo Cruz; BrasilFil: Almeida, Carlos Eduardo. Universidade Estadual de Campinas; Brasi
Claire Wheeler: Fearless Psychologist
No full textFearless physician/psychologist Claire is a clinical psychologist and former emergency room doctor. As a full-time instructor at PSU’s School of Community Health she teaches classes in disease physiology, mind-body medicine, nutrition and health psychology. She is the author of 10 Simple Solutions to Stress, published in 2007. She’ll reveal some of the mysteries of how negative thoughts can affect your health, and teach techniques to avoid them. Think “cognitive reframing.”https://pdxscholar.library.pdx.edu/pdxtalks/1020/thumbnail.jp
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