identifier	taxonID	type	CVterm	format	language	title	description	additionalInformationURL	UsageTerms	rights	Owner	contributor	creator	bibliographicCitation
8A245ADF197F5E3996445568C1814AF1.text	8A245ADF197F5E3996445568C1814AF1.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Acalypta alutacea Souma 2025	<div><p>Acalypta alutacea sp. nov.</p><p>Figs 1 A, B, 3 A – D, 5 A, 7 A – D, 9 A, 11 A, 13 A, B, 14 A, B, 15 A Japanese name: Kushiromaru-gunbai</p><p>Acalypta sp.: Nakatani (2016: 50) (distribution); Nakatani (2018: 48) (distribution).</p><p>Material examined.</p><p>Holotype, Japan • brachypterous ♂; Hokkaido, Kushiro-gun, Kushiro-cho,  Beppo; 27 Jun. 2024; J. Souma leg.; SIHU  .  Paratypes, Japan • 1 brachypterous ♂ 4 brachypterous ♀♀; same data as for holotype; SIHU •   1 brachypterous ♂ 1 brachypterous ♀; “ 春採湖北岸 ” [= Hokkaido, Kushiro-shi, Shunkodai,  North shore of Harutori Lake]; 8 Jul. 2015; M. Nakatani leg.; SIHU. Two specimens collected in 2015 were recorded as “  Acalypta sp. ” in a previous study (Nakatani 2016)  .</p><p>Diagnosis.</p><p>Acalypta alutacea sp. nov. is recognized among the other species of  Acalypta based on a combination of the following characteristics: brachypterous morph only known; hemelytron without dark spots (Fig. 1 A, B); antenniferous tubercle obtuse, curved inward (Figs 3 A – D, 13 A, B); basal part of antennal segment III not thickened; rostrum reaching anterior part of abdominal sternite II (Fig. 5 A); pronotum 3 / 4 times as long as maximum width across paranota; pronotal disc as long as calli; punctures on pronotal disc smaller than areolae of posterior process; posterior part of hood usually triangular; lateral carina of pronotum absent or reduced, shorter than hood, without or with a single minute areola; calli smooth; paranotum as wide as hood, not narrowed posteriorly, with 3–4 rows of areolae throughout its length; anterolateral angle of paranotum rounded, not or weakly protruding anteriorly, not reaching mid-level of compound eye; posterolateral angle of paranotum protruding posteriorly; posterior process strongly protruding posteriorly, as long as hood; costal area of hemelytron with 2–3 rows of areolae in basal part, a single row in middle part, and 1–2 rows in apical part (Fig. 7 A – D); discoidal area expanded beyond apical fourth of hemelytron, wider than subcostal area; Cu (cubitus) vein distinct throughout its length; abdomen pale brown in female (Fig. 11 A); and pygophore roundly inflated (Fig. 14 A).</p><p>Description.</p><p>Brachypterous male. Frontal spine of head, pronotum except for calli, hemelytron, and sternal laminae pale brown; antenniferous tubercle, antennal segments I to III, ventral surface of thorax except for sternal laminae, and legs brown; most parts of head, antennal segment IV, calli, and abdomen dark brown; paranotum and hemelytron sometimes irregularly dark in very small sections, without dark spots; areolae of pronotum and hemelytron transparent; compound eyes dark red; pubescence on body yellowish (Figs 1 A, 3 A, B, 5 A, 7 A, B, 9 A).</p><p>Body ovate; pubescence on most parts of body distinctly shorter than radius of compound eye (Figs 1 A, 3 A, B, 5 A, 9 A). Head covered with minute pubescence; pair of frontal spines separated at apices, reaching apex of clypeus; antenniferous tubercle obtuse, curved inward, shorter than frontal spine; vertex and clypeus smooth. Compound eye round in dorsal view. Antenna densely covered with minute pubescence in segments I to III and long pubescence in segment IV; pubescence on segment IV longer than pubescence on other parts of body; segment I cylindrical, shorter than segment IV; segment II conical, shortest amongst antennal segments; segment III linear, longest amongst antennal segments, not thickened in basal part; segment IV fusiform. Bucculae closed at anterior ends, with 3 rows of areolae at highest part. Rostrum reaching anterior part of abdominal sternite II.</p><p>Pronotum (Figs 3 A, B, 13 A, B) glabrous, 3 / 4 times as long as maximum width across paranota. Pronotal disc coarsely punctate, as long as calli; punctures smaller than areolae of posterior process. Hood roof-shaped, shorter than median carina of pronotum, wider than vertex at widest part, not covering compound eye, with 5 rows of areolae at highest part; posterior part usually triangular. Median carina straight, extending to apex of posterior process, with a single row of areolae throughout its length. Lateral carina absent or reduced, shorter than hood, without or with a single minute areola. Calli smooth. Paranotum horizontally expanding outward, as wide as hood, not narrowed posteriorly, with 3–4 rows of areolae throughout its length; anterolateral angle rounded, not or weakly protruding anteriorly, not reaching mid-level of compound eye; posterolateral angle protruding posteriorly. Posterior process triangular, obtuse at apex, strongly protruding posteriorly, as long as hood.</p><p>Hemelytron (Fig. 7 A, B) glabrous, extending beyond apex of abdomen; apex close to the other at rest; costal area with 2–3 rows of areolae in basal part, a single row in middle part, and 1–2 rows in apical part; subcostal area with 4 rows of areolae at widest part; discoidal area expanded beyond apical fourth of hemelytron, wider than subcostal area, with 4–5 rows of areolae at widest part; sutural area with 3 rows of areolae at widest part; hypocostal lamina with a single row of areolae throughout its length; Sc (subcosta), Hc (hypocosta), R + M (fused radius and media) and Cu (cubitus) veins distinct throughout their respective length.</p><p>Thoracic pleura (Fig. 5 A) smooth in anterior part, coarsely punctate in posterior part. Ostiolar peritreme reduced. Mesosternum narrower than metasternum. Sternal laminae lower than buccula, open in both anterior and posterior ends; metasternal lamina as high as mesosternal lamina. Legs (Fig. 1 A) smooth, covered with minute pubescence; femora thickest at middle.</p><p>Abdomen ovate in dorsal and ventral views, glabrous except for terminalia, smooth. Pygophore (Figs 9 A, 14 A) roundly inflated, semicircular in ventral view, covered with minute pubescence; anterior margin concave in middle part. Paramere (Fig. 14 B) slender, expanded in middle part, gently curved inward, covered with minute pubescence in middle part of outer and inner margins.</p><p>Measurements (n = 3). Body length with hemelytra 2.30–2.60 mm; maximum width across hemelytra 1.30–1.50 mm; length of antennal segments I to IV 0.15 mm, 0.10 mm, 0.70–0.80 mm, and 0.20–0.25 mm, respectively; pronotal length 0.70–0.80 mm; pronotal width across paranota 1.10–1.20 mm; hemelytral length 1.65–1.85 mm; maximum width of hemelytron 0.70–0.80 mm.</p><p>Brachypterous female. General habitus very similar to that of male (Figs 1 B, 3 C, D, 7 C, D, 11 A) except for the following characters: abdomen pale brown; body usually longer and wider than in male; antennal segment III shorter than in male; and apical part of abdomen pentagonal in ventral view.</p><p>Measurements (n = 5). Body length with hemelytra 2.60–2.80 mm; maximum width across hemelytra 1.65–1.80 mm; length of antennal segments I to IV 0.15 mm, 0.10 mm, 0.60 mm, and 0.20 mm, respectively; pronotal length 0.80–0.90 mm; pronotal width across paranota 1.20–1.30 mm; hemelytral length 1.90–2.00 mm; maximum width of hemelytron 0.85–0.95 mm.</p><p>Remarks.</p><p>Among all the species of  Acalypta,  A. alutacea sp. nov. strongly resembles  A. carinata and  A. platycheila (Fieber, 1844) in terms of its general habitus. However, based on a comparison between the type materials of the new species and the non-types and descriptions (Péricart 1978, 1983) of  A. carinata and  A. platycheila, five main characteristics were recognized to easily differentiate  A. alutacea sp. nov. from  A. carinata and  A. platycheila (Figs 1 A – D, 3 A – G, 7 A – G, 13 A – D): posterior part of pronotal hood usually triangular (usually semicircular in  A. platycheila); lateral carinae absent or reduced, shorter than hood, without or with a single minute areola (developed, as long as hood, with a single row of areolae in  A. carinata and  A. platycheila); calli smooth (rough in  A. platycheila); anterolateral angle of paranotum not or weakly protruding anteriorly, not reaching mid-level of compound eye (strongly protruding anteriorly, reaching mid-level of compound eye in  A. carinata and  A. platycheila); and costal area of hemelytron with 2–3 rows of areolae in basal part, a single row in middle part, and 1–2 rows in apical part (with usually a single row throughout its length and sometimes 2 rows in basal part in  A. platycheila). Morphological differences between the new species and the eight other Japanese species besides  A. carinata are presented in the identification key below.</p><p>Distribution.</p><p>Japan (Hokkaido) (Fig. 17) (Nakatani 2016, 2018).</p><p>Etymology.</p><p>The species epithet is the Latin adjective “ alutaceus ”, referring to the pale brown body color.</p><p>Host plant.</p><p>Six individuals of  Acalypta alutacea sp. nov. were collected from indeterminate mosses growing on the forest floor; at least one of these mosses could be a host plant for the new species.</p><p>Bionomics.</p><p>Acalypta alutacea sp. nov. inhabits the forest floor of deciduous broad-leaved forests in Hokkaido, which has a cool temperate climate.</p><p>Adults were collected in June and July (Nakatani 2016, 2018) but nymphs were not collected.</p></div>	https://treatment.plazi.org/id/8A245ADF197F5E3996445568C1814AF1	Public Domain	No known copyright restrictions apply. See Agosti, D., Egloff, W., 2009. Taxonomic information exchange and copyright: the Plazi approach. BMC Research Notes 2009, 2:53 for further explanation.		Pensoft via Plazi	Souma, Jun	Souma, Jun (2025): A new species and two new records of the moss-feeding lace bug genus Acalypta (Hemiptera, Heteroptera, Tingidae) from Hokkaido, northern Japan, with an illustrated key to the Japanese species of the genus. ZooKeys 1229: 107-132, DOI: 10.3897/zookeys.1229.142344
E3A239E19528595FAC3C9484B4E62C9B.text	E3A239E19528595FAC3C9484B4E62C9B.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Acalypta carinata (Panzer 1806)	<div><p>Acalypta carinata (Panzer, 1806)</p><p>Figs 1 C, D, 3 E – G, 5 B, 7 E – G, 9 B, 11 B, 13 C, D, 15 B – D Japanese name: Yachimaru-gunbai</p><p>Tingis carinata Panzer, 1806: 631 . Syntype (s): sex unknown; type locality: Germany • “ Mannheimii ” [= Mannheim]; depository: unknown.</p><p>Acalypta carinata: Westwood (1840: 121) (new combination).</p><p>Note.</p><p>For synonyms and detailed descriptions of the species see Drake and Ruhoff (1965), Péricart (1978, 1983), and Péricart and Golub (1996).</p><p>Material examined.</p><p>Non-types,   Japan • 1 brachypterous ♀; Hokkaido, Soya-gun, Sarufutsu-mura,  Sarufutsu; 15 Aug. 2023; J. Souma leg.; SIHU  •  3 brachypterous ♂♂ 1 brachypterous ♀ 7 fifth instar nymphs; same collection data as for preceding; 29 Sep. 2023; adults have emerged until 26 Oct. 2023 by fed on mosses growing on marshlands in captivity; SIHU •   1 brachypterous ♂ 1 brachypterous ♀ 2 fifth instar nymphs; Rishiri Island, Rishirifuji-cho,  Oshidomari; 28 Sep. 2024; R. Wakimura leg.; adults have emerged until 15 Nov. 2024 by fed on mosses growing on forest floor of deciduous broad-leaved forests in captivity; SIHU  •   1 brachypterous ♀ 1 fifth instar nymph; Rishiri Island, Rishiri-cho,  Kutsugata; 29 Sep. 2024; R. Wakimura leg.; adult has emerged until 30 Nov. 2024 by fed on mosses growing on forest floor of deciduous broad-leaved forests in captivity; SIHU  .</p><p>Remarks.</p><p>The 18 specimens recorded above (Fig. 1 C, D) matched well with the descriptions and illustrations of  Acalypta carinata (Péricart 1978, 1983) in terms of their morphological characteristics, particularly the structures of the pronotum and hemelytron (Figs 3 E – G, 7 E – G, and Fig. 13 C, D). Therefore, the specimens examined were identified as  A. carinata .</p><p>Acalypta carinata is most similar to  A. platycheila in general appearance, but the former can be distinguished from the latter based on the following characters (Figs 3 E – G, 7 E – G, 13 C, D) (cf. Péricart 1978, 1983): posterior part of pronotal hood usually triangular (usually semicircular in  A. platycheila); lateral carinae slightly close to each other toward anterior ends (parallel or slightly separated in  A. platycheila); calli smooth (rough in  A. platycheila); and costal area of hemelytron with usually 2 rows of areolae throughout its length, sometimes 3 rows in basal part, and sometimes a single row in middle part (with usually a single row throughout its length and sometimes 2 rows in basal part in  A. platycheila). Morphological differences between  A. carinata and the nine other Japanese species are presented in the identification key below.</p><p>The teratological form of the pronotum and hemelytron was confirmed in  A. carinata from Japan, and one examined specimen possessed malformations of the right paranotum and hemelytron (Figs 1 D, 3 G, 7 G), as reported in many lace bugs (Štusák and Stehlík 1980, 1982).</p><p>Distribution.</p><p>Austria, Belgium, Byelorussia, Croatia, Czech Republic, Denmark, Estonia, Finland, France, Great Britain, Germany, Hungary, Ireland, Italy, Japan (Hokkaido, Rishiri Island), Latvia, Luxembourg, Moldovia, Mongolia, Netherlands, Norway, Poland, Romania, Russia, Slovakia, Slovenia, Spain, Sweden, Switzerland (Fig. 17) (Péricart and Golub 1996; Aukema et al. 2013; Aukema 2025).  Acalypta carinata is newly recorded from Japan.</p><p>Host plant.</p><p>The Japanese population of  Acalypta carinata feeds on indeterminate mosses growing in marshlands or the forest floor of deciduous broad-leaved forests in captivity. In other distribution areas,  Abietinella abietina (Hedw.) M. Fleisch. ( Thuidiaceae), and indeterminate mosses have been recorded as host plants for this species (cf. Drake and Ruhoff 1965; Péricart 1983).</p><p>Bionomics.</p><p>Acalypta carinata is found only in marshlands in Hokkaido, Japan and is dominant among  Acalypta species in humid environments, such as marshlands and riparian forests in Hungary (Rédei et al. 2004), suggesting that it mainly inhabits humid environments regardless of the region. However, this species inhabits the forest floor of deciduous broad-leaved forests exceptionally on Rishiri Island, near Hokkaido, where no other  Acalypta species has been recorded.</p><p>In Japan, adults and nymphs were observed in August and September, respectively. In Europe, adults were collected between April and October, and nymphs were confirmed in almost all seasons; the overwintering stage comprised nymphs (cf. Péricart 1983; Rédei et al. 2004).</p></div>	https://treatment.plazi.org/id/E3A239E19528595FAC3C9484B4E62C9B	Public Domain	No known copyright restrictions apply. See Agosti, D., Egloff, W., 2009. Taxonomic information exchange and copyright: the Plazi approach. BMC Research Notes 2009, 2:53 for further explanation.		Pensoft via Plazi	Souma, Jun	Souma, Jun (2025): A new species and two new records of the moss-feeding lace bug genus Acalypta (Hemiptera, Heteroptera, Tingidae) from Hokkaido, northern Japan, with an illustrated key to the Japanese species of the genus. ZooKeys 1229: 107-132, DOI: 10.3897/zookeys.1229.142344
78A92F96FB6557BC83B4504429BB3B11.text	78A92F96FB6557BC83B4504429BB3B11.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Acalypta sauteri Drake 1942	<div><p>Acalypta sauteri Drake, 1942</p><p>Figs 2 E, 4 E, 6 C, 8 E, 10 C, 12 C, 16 C, D Japanese name: Maru-gunbai</p><p>Acalypta sauteri Drake, 1942: 14. Holotype: brachypterous ♂; type locality: Japan • Oayama [= Honshu, Kanagawa-ken, Mt. Oyama] (cf. Takeya 1951; Miyatake 1958; Hiura 1960; Drake and Lattin 1963; Tomokuni 1983); depository: United States National Museum of Natural History, Washington, D. C., USA.</p><p>References.</p><p>Takeya (1951: 6) (checklist: eastern Asia); Miyatake (1958: 15) (distribution); Hiura (1960: 70) (distribution); Takeya (1962: 68) (distribution); Drake and Lattin (1963: 336) (distribution); Drake and Ruhoff (1965: 54) (catalogue); Miyamoto (1965: 90) (monograph); Tomokuni (1972: 88) (distribution); Baba (1982: 8) (distribution); Tomokuni (1983: 146) (biology); Tomokuni (1985: 156) (distribution); Miyamoto and Yasunaga (1989: 166) (checklist: Japan); Takahashi (1990: 3) (distribution); Péricart and Golub (1996: 10) (checklist: Palaearctic); Miyamoto (2008: 157) (monograph); Yamada and Tomokuni (2012: 187) (monograph); Yano et al. (2013: 24) (distribution); Maehara (2014: 57) (distribution); Nozaki et al. (2016: 75) (distribution); Yamada and Ishikawa (2016: 429) (checklist: Japan); Hayashi and Kadowaki (2018: 309) (checklist: Oki Islands); Ito and Sasaki (2018: 17) (distribution); Obae (2019: 18) (distribution); Okochi (2019: 1) (distribution); Yamaguchi and Nakamura (2019: 61) (distribution); Yoshitomi and Hayashi (2019: 84) (distribution); Kawase (2020: 6) (distribution); Konno (2020: 18) (distribution); Yamamoto (2021 a: 4) (distribution); Takai (2022: 61) (distribution); Konno (2023: 18) (distribution); Okochi (2023: 5) (distribution); Yamamoto (2022 a: 2) (distribution); Yamamoto (2022 b: 10) (distribution); Ban et al. (2024: 115) (distribution); Yamamoto (2024 a: 4) (distribution); Yamamoto (2024 b: 9) (distribution).</p><p>Material examined.</p><p>Non-types,   Japan • 1 brachypterous ♂; Hokkaido, Yakumo-cho,  Namarikawa; 29 Jun. 2024; R. Sato leg.; SIHU  •  2 brachypterous ♀♀; same collection data as for preceding; 6 Oct. 2024; SIHU •   1 brachypterous ♂ 1 brachypterous ♀; Awa Island,  Uramura; 20 Sep. 2015; G. Mashima leg.; TUA  .</p><p>Remarks.</p><p>Although  Acalypta sauteri exhibits geographic variations (Tomokuni 1972), the morphological characteristics of the above five specimens were consistent with photographs of the holotype (United States National Museum of Natural History 2024) and the original description (Drake 1942) of the species. Therefore, we identified the studied specimens from Hokkaido and Awa Island as  A. sauteri . Morphological differences between  A. sauteri and nine other Japanese species are provided in the identification key below.</p><p>Distribution.</p><p>Japan (Hokkaido, Honshu, Awa Island, Sado Island, Awaji Island, Oki Islands (Dogo Island), Ikuchi Island, Shikoku, Shodo Island, Omi Island, Kyushu, Amakusa Islands (Shimoshima Island)) (Fig. 17) (Tomokuni 1983, 1985; Nozaki et al. 2016; Yamada and Tomokuni 2012; Yamada and Ishikawa 2016; Aukema 2025).  Acalypta sauteri is newly recorded from Hokkaido and Awa Island. The discovery of  A. sauteri from Hokkaido also represents the northernmost record of this species.</p><p>Host plant.</p><p>Acalypta sauteri were collected from 23 moss species belonging to 14 families:  Atrichum rhystophyllum (Müll. Hal.) Paris ( Polytrichaceae),  Brachythecium buchananii (Hook.) A. Jaeger ( Brachytheciaceae),  B. plumosum (Hedw.) Bruch et Schimp,  B. populeum (Hedw.) Bruch et Schimp.,  B. rivulare Bruch et Schimp.,  Brotherella henonii (Duby) M. Fleisch. ( Pylaisiadelphaceae),  Bryhnia trichomitria Dixon et Thér. ( Brachytheciaceae),  Codriophorus anomodontoides (Cardot) Bednarek-Ochyra et Ochyra ( Grimmiaceae),  Cratoneuron filicinum (Hedw.) Spruce ( Amblystegiaceae),  Entodon sullivantii (Müll. Hal.) Lindb. ( Entodontaceae),  Haplocladium microphyllum (Hedw.) Broth. ( Leskeaceae),  Hypnum cupressiforme Hedw. ( Hypnaceae),  H. oldhamii (Mitt.) A. Jaeger et Sauerb.,  H. plumaeforme Wilson,  H. tristoviride (Broth.) Paris,  Kindbergia arbuscula (Broth.) Ochyra ( Brachytheciaceae),  Leptodictyum riparium (Hedw.) Warnst. ( Amblystegiaceae),  Philonotis thwaitesii Mitt. ( Bartramiaceae),  Plagiomnium acutum (Lindb.) T. J. Kop. ( Mniaceae),  Plagiothecium euryphyllum (Cardot et Thér.) Z. Iwats. ( Symphyodontaceae),  Rosulabryum billardieri (Schwägr.) J. R. Spruce ( Bryaceae),  Trachycystis microphylla (Dozy et Molk.) Lindb. ( Mniaceae), and  Thuidium kanedae Sakurai ( Thuidiaceae) (Tomokuni 1983, 1985; Yamada and Tomokuni 2012; Yamamoto 2022 a; Ban et al. 2024).</p><p>Bionomics.</p><p>Adults were observed in almost all seasons, and nymphs were collected in January and May, and from August to October (Drake 1942; Takeya 1951, 1962; Miyatake 1958; Hiura 1960; Drake and Lattin 1963; Tomokuni 1972, 1983, 1985; Baba 1982; Takahashi 1990; Yamada and Tomokuni 2012; Yano et al. 2013; Maehara 2014; Nozaki et al. 2016; Ito and Sasaki 2018; Yamaguchi and Nakamura 2019; Obae 2019; Okochi 2019, 2023; Yoshitomi and Hayashi 2019; Kawase 2020; Konno 2020, 2023; Yamamoto 2021 a, 2022 a, 2022 b, 2024 a, 2024 b; Takai 2022; Ban et al. 2024), suggesting that the overwintering stage is characterized by adults and nymphs.</p></div>	https://treatment.plazi.org/id/78A92F96FB6557BC83B4504429BB3B11	Public Domain	No known copyright restrictions apply. See Agosti, D., Egloff, W., 2009. Taxonomic information exchange and copyright: the Plazi approach. BMC Research Notes 2009, 2:53 for further explanation.		Pensoft via Plazi	Souma, Jun	Souma, Jun (2025): A new species and two new records of the moss-feeding lace bug genus Acalypta (Hemiptera, Heteroptera, Tingidae) from Hokkaido, northern Japan, with an illustrated key to the Japanese species of the genus. ZooKeys 1229: 107-132, DOI: 10.3897/zookeys.1229.142344
13EE1A698E1F5BA9AEB3885895437871.text	13EE1A698E1F5BA9AEB3885895437871.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Acalypta Westwood 1840	<div><p>Genus  Acalypta Westwood, 1840</p><p>Acalypta Westwood, 1840: 121 . Type species by original designation:  Tingis carinata Panzer, 1806 .</p><p>Note.</p><p>For synonyms and detailed descriptions of the genus see Drake and Lattin (1963), Péricart (1978, 1983), and Péricart and Golub (1996).</p><p>Remarks.</p><p>The genus  Acalypta, which is distributed only in the northern hemisphere, previously comprised 46 species (cf. Souma 2019, 2023 a), but in this study, the author describes a new species,  A. alutacea sp. nov., increasing the number of species to 47. Among them, the following eight species have been known from Japan:  A. cooleyi;  A. gracilis;  A. hirashimai;  A. marginata;  A. miyamotoi;  A. pallidicoronata;  A. sauteri; and  A. tsurugisana (Yamada and Ishikawa 2016; Souma 2019, 2020, 2021, 2023 a). However, with the description of  A. alutacea sp. nov. and the first record of  A. carinata from Japan, a total of ten  Acalypta species are currently recognized.</p></div>	https://treatment.plazi.org/id/13EE1A698E1F5BA9AEB3885895437871	Public Domain	No known copyright restrictions apply. See Agosti, D., Egloff, W., 2009. Taxonomic information exchange and copyright: the Plazi approach. BMC Research Notes 2009, 2:53 for further explanation.		Pensoft via Plazi	Souma, Jun	Souma, Jun (2025): A new species and two new records of the moss-feeding lace bug genus Acalypta (Hemiptera, Heteroptera, Tingidae) from Hokkaido, northern Japan, with an illustrated key to the Japanese species of the genus. ZooKeys 1229: 107-132, DOI: 10.3897/zookeys.1229.142344
