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FIGURE 4 in A new genus for "Neocallichirus" grandis Karasawa & Goda, 1996, a ghost shrimp species (Decapoda: Axiidea: Callianassidae) heretofore known only by fossil materials
No full textFIGURE 4. Laticallichirus grandis (Karasawa & Goda, 1996) n. comb.. A, B, D, E, H–J, male (18.2 mm), CBM-ZC 15247; C, F, G, female (cl 16.1 mm), CBM-ZC 15249. A, left maxilliped 3, outer view; B, same, inner view (setae partially omitted); C, left pereopod 2, outer view; D, right pereopod 3, outer view; E, same, carpus to dactylus, inner view (setae omitted); F, right pereopod 4, outer view; G, same, propodus and dactylus, inner view (setae omitted); H, same, details of fixed finger of propodus, outer view; I, left pereopod 5, outer view; J, same, chela, inner view.Published as part of Komai, Tomoyuki, Yokooka, Hiroyuki, Henmi, Yumi & Itani, Gyo, 2019, A new genus for "Neocallichirus" grandis Karasawa & Goda, 1996, a ghost shrimp species (Decapoda: Axiidea: Callianassidae) heretofore known only by fossil materials, pp. 461-481 in Zootaxa 4604 (3) on page 471, DOI: 10.11646/zootaxa.4604.3.4, http://zenodo.org/record/285248
FIGURE 5 in Redescription of Pinnixa haematosticta Sakai, 1934, its transfer to Indopinnixa Manning & Morton, 1987, and a reappraisal of Indopinnixa kumejima Naruse & Maenosono, 2012 (Decapoda: Brachyura: Pinnotheridae)
No full textFIGURE 5. Indopinnixa haematosticta (Sakai, 1934) n. comb., male (3.6×8.3 mm), CBM-ZC 15291. A, entire thoracic sternum, ventral view (setae omitted; gonopods omitted); B, anterior thoracic sternites, ventral view (perpendicular to horizontal plane; gonopods dissected); C, right edge of sterno-pleonal cavity of thoracic sternites 5 and 6, ventrolateral view; D, right thoracic sternites 7 and 8 and pleomeres 1 and 2, posterior view; E, pleon and telson, ventral (external) view; F, pleomeres 3–6, dorsal (internal) view; G, right gonopod 1, ventral view; H, same, distal part, dorsal view; I, right gonopod 2.Published as part of Komai, Tomoyuki, Naruse, Tohru, Yokooka, Hiroyuki, Taru, Masanori, Shimetsugu, Miho & Watanabe, Tetsuya, 2022, Redescription of Pinnixa haematosticta Sakai, 1934, its transfer to Indopinnixa Manning & Morton, 1987, and a reappraisal of Indopinnixa kumejima Naruse & Maenosono, 2012 (Decapoda: Brachyura: Pinnotheridae), pp. 361-389 in Zootaxa 5100 (3) on page 371, DOI: 10.11646/zootaxa.5100.3.3, http://zenodo.org/record/620160
Indopinnixa haematosticta Komai & Naruse & Yokooka & Taru & Shimetsugu & Watanabe 2022, n. comb.
No full textIndopinnixa haematosticta (Sakai, 1934) n. comb. (Figs. 2–8, 16) Pinnixa haematosticta Sakai, 1934: 42, fig. 3 [type locality: off Kisami, Shimoda, Izu Peninsula]; 1935: 203, fig. 107, pl. 57, fig. 4 (holotype); 1939: 600, text-fig. 85, pl. LXX, fig. 4 (holotype); 1976: 585, fig. 323, pl. 202, fig. 3 (holotype).— Yamauchi & Konishi 2005: 1241, fig. 1F (holotype).— Komatsu & Takeda 2009: 201 (off Ogi, Noto-cho, Ishikawa Prefecture; off Taniyama, Kagoshima Prefecture), 203 (key). Pinnixa hematosticta. — Ng et al. 2008: 247 (list). Not Pinnixa haematosticta: Miyake 1983: 155, pl. 52-4 (Ezura, Nanki-shirahama, Wakayama Prefecture). –– Watanabe 2012: 217, colour fig. (Matsushima, Amakusa, Kumamoto Prefecture). Records need to be verified: Pinnixa haematosticta.— Miyake 1961: 175 (Ariake Sea).— Miyake et al. 1962: 130 (Ariake Sea).— Nagai, 1990: 116 (Nankishirahama, Wakayama Prefecture).— Marumura & Kosaka 2003: 68 (Tsuchiya, Ehime Prefecture). Type material. Holotype: KPM-NH107899, female (2.9× 6.9 mm), off Kisami, Shimoda, Izu Peninsula, Japan, 20 fathoms, sandy bottom, mixed with dead shells. Other material examined. Honshu: CBM-ZC 15286, 1 male (2.5× 5.3 mm), Ena Bay, Miura Peninsula, Kanagawa Prefecture, intertidal, inhabiting tube of terebellid worm, 13 April 2013, digging with shovel, coll. T. Unagami and M. Taru; CBM-ZC 15287, 1 ovigerous female (4.2× 9.2 mm), same locality, intertidal, 26 July 2014, digging with shovel, coll. K. Yokoyama; CBM-ZC 15288, 1 female (3.2× 7.4 mm), same locality, 7 June 2015, digging with trowel, coll. M. Taru; RUMF-ZC-5948, 1 male (3.2× 6.5 mm), Tagoshi River estuary, Zushi, Kanagawa Prefecture, 23 April 2019, coll. H. Nakajima; RUMF-ZC-5949, 1 male (2.7× 5.8 mm), Aburatsubo, Miura, Kanagawa Prefecture, 24 May 2019, coll. H. Nakajima; CBM-ZC 15290, 2 females (3.5×7.6, 3.5× 7.8 mm, latter specimen DNA voucher), Tsumeki-zaki, Shimoda, Shizuoka Prefecture, shallow subtidal, 21 September 2016, yabby pump, coll. H. Yokooka; CBM-ZC 15291, 1 male (3.6× 8.3 mm), 1 female (4.1× 8.5 mm), same locality, 3 December 2016, yabby pump, coll. H. Yokooka; CBM-ZC 15289, 1 androgynous specimen (2.6× 5.6 mm), Kujyuppama, Shimoda, Shizuoka Prefecture, sand flat, 16 September 2016, coll. H. Yokooka; CBM-ZC 15292, 1 androgynous specimen (2.7× 5.6 mm), Uramura, Toba, Mie Prefecture, intertidal, 20 June 2015, digging, coll. M. Shimetsugu; CBM-ZC 15293, 1 female (2.7× 5.8 mm), same locality, 2 April 2017, digging, coll. M. Shimetsugu; CBM-ZC 9135, 1 androgynous specimen (2.5× 4.7 mm), Fukaura, Kasado Island, Shimomatsu, Yamaguchi Prefecture, intertidal sand flat, 13 October 2002, digging with shovel, coll. H. Fukuda. Kyushu: RUMF-ZC-6000, 3 ovigerous females (2.8×5.8, 3.0×6.1, 3.1× 6.8 mm, second specimen DNA voucher), Kamenokojima, Sasebo, Nagasaki Prefecture, 33.1259N, 129.6783E, 3 October 2017, coll. T. Naruse & P. K. L. Ng; CBM-ZC 15294, 2 females (2.8×6.0, 2.8× 6.4 mm), Aitsu, Matsushima, Kami-Amakusa, Kumamoto Prefecture, intertidal, 21 April 2004, coll. T. Watanabe; CBM-ZC 15295, 1 ovigerous female (2.8× 6.6 mm), same locality, 11 July 2006, coll. T. Watanabe; CBM-ZC 15296, 1 female (2.3× 5.7 mm), same locality, 12 March 2008, coll. T. Watanabe; NSMT-Cr 6470, 2 males (3.0×6.4, 3.5× 7.4 mm), 3 females (3.3×7.0–3.6× 7.5 mm), off Taniyama, Kagoshima Bay, 30–50 m, 7 May 1970; RUMF-ZC-5955, 9 males (1.8×3.3–2.9× 6.1 mm), 5 females (1.9×3.7–3.1× 6.4 mm), 15 ovigerous females (1.9×3.9–3.0× 6.8 mm), Fukiage Beach, Kominato, Minami Satsuma, Satsuma Peninsula, Kagoshima Prefecture, beach combing after typhoon, 20 September 2016, coll. D. Uyeno; CBM-ZC 16586, 3 males (2.7×5.5–2.9× 6.1 mm), 3 ovigerous females (2.9×6.0, 3.2×6.6, 3.3× 6.9 mm, first specimen DNA voucher), same data; CBM-ZC 15297, 1 male (2.5× 5.5 mm), 1 female (4.0× 9.1 mm), Kumano Fishing Port, Naka-Tane, Tanegashima Island, 0.5 m at low tide, 18 May 2018, yabby pump, coll. T. Komai. Redescription. Male. Body and appendages well-sclerotized. Carapace (Figs. 2A; 3–C) transversely ovate, 2.1–2.3 times wider than long; dorsal surface gently convex in general, sparsely punctate, with very short, pigmented setae on front and adjacent to anterior margin; regions poorly defined, only shallow, median gastrocardiac groove discernible; cardiac region transversely elevated, with low but clearly delimited transverse ridge falling far short of posterolateral margins. Front slightly bilobed, slightly more than 0.1 times carapace width; lateral angle bluntly angular. Supraorbital margin entire, slightly limbed laterally, confluent with suborbital margin; suborbital margin smooth, entire. Hepatic region slightly swollen. Anterolateral margin gently arcuate, defined by granular ridge not confluent with supraorbital margin, starting some distance from orbit, forming distinct projection at juncture with posterolateral margin; posterolateral margin smooth, slightly sinuous, distinctly converging towards almost straight posterior carapace margin. Subhepatic region with low oblique ridge obscured by numerous short, plumose setae; suborbital region narrow; pterygostomial regions smooth. Ocular peduncle (Figs. 2A, 3A–C) filling orbit, stout, with scattered very short, darkly pigmented setae on dorsal surface; cornea narrower than ocular peduncle, darkly pigmented. Antennule (Fig. 3B, C) with basal articles sub-globular, separated by median septum; distal 2 articles folded transversely; article 3 slightly longer than article 2; upper and lower flagella both shorter than article 3. Antenna with subquadrate basal article in contact with orbit; flagellum short. Epistome (Fig. 3C) longitudinally very narrow, posteromedian margin protruded into buccal space as short ridge; anterior buccal flame gently convex on either side of median ridge, with distinct suture at base of antennal article 1. Maxillipeds 3 with large propodi and dactyli (Fig. 3D, E), endopod and its setae filling most of buccal space. Ischium and merus completely fused to form subtriangular plate (= ischiomerus), external surface without median sulcus, but keeled along inner margin, outer margin obscured by numerous short to long plumose setae. Carpus shorter than ischiomerus, outer surface with numerous short plumose setae. Propodus subovate, spatuliform, with scattered short plumose setae on external surface. Dactylus also spatuliform, articulated at middle portion of flexor margin of propodus, widest at distal 0.25 length, distal part wider than proximal, tip rounded. Inner margins of ischiomerus and carpus, inner to distal margin of propodus, and inner margin of dactylus with very long, thick setae for filter feeding. Exopod completely hidden by outer margin of ischiomerus, shorter than ischiomerus, tapering distally, outer margin with subtriangular lobiform structure at about midlength; flagellum much shorter than exopod. Chelipeds (Figs. 2A, B; 4A) not enlarged; subequal and similar. Basis and ischium fused but suture visible, surfaces almost glabrous. Merus relatively short, without conspicuous armature, most surfaces obscured by plumose setae; upper surface almost flat, with few granules on proximal outer portion; inner margin convex, with row of granules; outer surface rounded; lower surface glabrous, with row of granules along outer side. Carpus short, cupshaped, also without conspicuous armature; upper surface with few short setae. Chela 1.9–2.2 times as long as high, fairly compressed; lower margin slightly sinuous. Palm 1.3–1.4 times as long as high; upper margin delimited by row of granules, obscured by numerous setae; outer surface with numerous short plumose setae obscuring scattered granules on upper half and having median longitudinal row of granules accompanied by short setae; inner surface with sparse, very short setae on dorsal side and numerous short to long plumose setae adjacent to lower margin; lower margin rounded, not carinate; fingers with wide hiatus filled by plumose setae; fixed finger nearly straight, not deflexed, terminating in small curved tip, occlusal margin with 2 or 3 blunt teeth at least in distal half. Dactylus 0.8 times as long as palm, noticeably curved, leaving distinct hiatus when closed; upper margin smooth or with row of minute granules and numerous plumose setae, occlusal margin armed with 1 small tooth at midlength. Ambulatory legs moderately long, pereopod 4 largest, pereopod 5 smallest. Pereopod 2 (Fig. 2A, B; 4B, C) moderately slender. Basis-ischium fused article short, with few granules on posterior margin. Merus slightly recurved, slightly narrowed distally, subtriangular in cross section; anterior surface non-carinate, with row of plumose setae; posterior surface with row of setae on upper side, otherwise almost glabrous. Carpus with extensor margin sharply carinate, flexor margin rounded with row of plumose seta on upper side. Propodus almost glabrous, 0.9–1.4 times as long as wide, 0.5–0.7 length of carpus; extensor margin sharply carinate, noticeably convex in large specimens; flexor margin also sharply carinate, less convex than upper margin. Dactylus nearly straight, 1.5 times as long as propodus, tapering to small corneous tip, with 4 distinct longitudinal carinae (extensor and flexor margins sharply carinate, upper and lower surfaces also each with median carina); extensor margin with short sparse setae. Pereopod 3 (Figs. 2A, B; 4D, E) moderately slender. Basis-ischium fused article short, with some granules on posterior face. Merus compressed, anterior margin bluntly carinate, nearly straight, with row of short to long plumose setae over entire length and row of small granules at least on proximal half; posterior surface bicarinate distally, with row of plumose setae on over entire length and row of granules at least on proximal half of upper side; upper and lower surfaces glabrous. Carpus with extensor margin gently convex and sharply carinate; flexor surface rounded with row of short to long plumose setae. Propodus 1.2–1.8 times as long as wide, almost glabrous except for row of short setae on flexor margin; extensor margin noticeably convex, sharply carinate; flexor margin gently convex, sharply carinate. Dactylus nearly straight, 1.5 times as long as propodus, tapering to small corneous tip, with 4 distinct longitudinal carinae (extensor and flexor margins sharply carinate, outer and inner surfaces also each with median carina); upper surface with row of short stiff setae on space between extensor and upper carinae. Pereopod 4 (Figs. 2A, B; 4F, G) stout, large, fairly compressed. Coxa enlarged, with prominent, glabrous lobe anteroventrally. Basis-ischium fused article with flat posterior surface, with few granules distally. Merus subovate, compressed, 1.7–2.0 times longer than wide; anterior margin gently convex, carinate, with rows of coarse granules and of plumose setae; upper surface with scattered coarse granules adjacent to anterior margin, obscured by plumose setae; lower surface smooth, glabrous; posterior surface concealed by dense plumose setae, flanked by carinae, upper carina delimited with single or double row of granules, becoming obsolete proximally, and with row of plumose setae; lower carina distinct over entire length, slightly sinuous, bordered with coarse granules. Carpus short, widened distally; extensor margin sharply carinate; upper surface with scattered short plumose setae; lower surface glabrous; flexor surface forming shallow concavity accommodating posterodistal angle of merus, defined on upper side by row of granules. Propodus tapering distally, 1.6 times as long as wide; extensor margin slightly convex, sharply carinate; upper surface with scattered short setae; lower surface glabrous; flexor surface flanked by sharp, granulate carinae, with dense plumose setae. Dactylus almost straight, subequal in length to propodus, tapering to small corneous claw, with 5 longitudinal carinae and sparse short setae; flexor surface narrow, with 2 longitudinal rows of short setae. Pereopod 5 (Figs. 2A, B; 4H) short, fairly compressed, falling far short of distal margin of merus of pereopod 4 when extended, with numerous long plumose setae on margins. Coxa with prominent knob-like protuberance on dorsodistal margin. Basis-ischium fused article with few granules on posterior surface. Merus twice as long as wide, anterior margin bluntly carinate, granulate; upper and lower surfaces almost glabrous; posterior surface flanked by sharp, granulate carinae, with numerous plumose setae. Carpus extensor margin non-carinate; upper and lower surfaces almost glabrous. Propodus subquadrate, 1.2 times as long as wide, extensor margin not carinate; upper and lower surfaces almost glabrous; posterior surface thickly setose. Dactylus subequal in length to propodus, subconical, with 2 rows of short stiff setae on extensor margin. Thoracic sternum (Figs. 2B; 5A, B, D) wide, polished, edges of sternites abutting sutures granular or smooth. Sternites 1 and 2 incompletely fused, deeply sunken into buccal cavity together with anteromedian part of sternite 3, obscured by thick setae; only lateral parts of sternite 3 clearly visible. Sternite 3 and 4 clearly separated by distinct, granulate ridge; distal part of gonopod 1 fitted into oblique lateral part of sternite 3. Sternite 4 with granules anteriorly; each anterolateral margin produced into rounded lobe, separated by anterolateral angle of sternite 3 by deep notch. Sternites 5–7 almost smooth, sternite 7 longitudinally widest. Sternite 8 wide, fully exposed, widened toward lateral margin, nearly perpendicular against horizontal plane of carapace, but partially visible in dorsal view, with transverse rows of setae, not extending to lateral margin, on midline and on morphologically anterior margin along suture, extending over entire width. Sterno-pleonal cavity deep, reaching to base of buccal cavity, marked by distinct ridges where sternites fit against lateral margins of closed pleon; margins of sterno-pleonal cavity along sternites 4–6 smooth, not granular; those on sternites 5 and 6 posteriorly raised to form prominent tubercles that grip closed pleon (Fig. 5C); press-button pleonal locking mechanism reduced into tiny tubercle inside of sterno-pleonal cavity of sternite 5 near suture between sternites 4/5. Penis sternal. Pleon (Figs. 2B; 5E, F) narrow, constricted, outer surface polished. Somites 1 and 2 transversely wide and very short, somite 1 with transverse row of short setae on midline. Somite 3 widest, trapezoidal, lateral margins rounded proximally. Somites 4–6 functionally fused, immobile although sutures clearly visible; somite 4 trapezoidal, lateral margins with shallow concavity corresponding to ledge-like structure on thoracic sternite 6; somite 5 subquadrate, lateral margins sinuous, concavities corresponding to ledge-like structure on thoracic sternite 5; somite 6 widened distally, with lateral margins concave; gonopodal plate absent. Telson covering posterior part of buccal cavity, almost as wide as pleomere 3, about 2 times as wide as long; lateral margin strongly convex, distal margin bilobed with shallow median notch. Male gonopod 1 (Fig. 5G, H) relatively long, somewhat compressed, reaching posterior end of buccal cavity, gently curved outward, outer and inner margins with row of numerous long, plumose setae; distal process delimited by slight constriction at base, strongly compressed, faintly recurved, terminal margin blunt, with patch of dense very short stiff setae on distal half of dorsal surface; shoulder at base of distal process with tuft of numerous long setae reaching to terminus of distal process. Male gonopod 2 very short, gently curved, with slightly inflated, spatuliform tip, less than 0.2 length of gonopod 1; base strongly inflated. Female. Carapace (Figs. 6A; 7A) generally similar to that of males (2.2 times as wide as long in holotype), but anterolateral margins slightly more sloping; cardiac region usually with distinct transverse ridge. Chela (Figs. 6A, B; 7B) proportionally smaller than in males, 2.3–2.5 times as long as high; lower margin nearly straight or faintly sinuous. Palm 1.4–1.6 times as long as high; upper margin with row of granules; outer surface with scattered granules superior to median line of setae; occlusal margin of fixed finger with row of 3–5 small blunt teeth. Dactylus 0.7–0.8 times as long as palm, curved distally, terminating in acute tip; upper margin gently arcuate, with row of granules; occlusal margin with 1 small but conspicuous tooth at about mid-length, and with row of minute teeth distal to median tooth. Pereopods 2–5 relatively shorter than in males (cf. Fig. 6A, B versus Fig. 2A, B; Fig. 7C–G). Pereopod 2 propodus slightly wider than long (1.1 times as wide as long in holotype) to 1.3 times as long as wide. Pereopod 3 propodus 1.3–1.6 times as long as wide. Pereopod 4 merus 1.7–1.9 times as long as wide. Female thoracic sternum (Fig. 6B) with most surfaces smooth or only slightly punctate, sometimes with sparse setae partially; lateral parts of sternites 4–8 exposed, not concealed by closed pleon (but developed setae on lateral margins of pleon sometimes covering lateral parts of sternite). Sternites 3 and 4 completely fused; widely concave anterior margin fringed with dense setae. Gonopore tubercle (vulva) small, low, generally rounded, extending anteriorly across half-length of sternite 6, overreaching more than half length of sternite 5; gonopore rounded (Fig. 7I). Pleon (Figs. 6B; 7H) relatively narrow (lateral parts of thoracic sternum exposed), subcircular, somite 4 widest; in ovigerous females, lateral margins fringed with thick setae covering lateral parts of thoracic sternum. Telson (Fig. 7H) 3.1–3.3 times as wide as long, reaching to bases of maxilliped 3, distal margin straight or slightly concave. Colouration in life. Base color of body and appendages gray-brown or brown, sometimes mottled, on dorsal side, whitish or pale yellow-brown on ventral side; carapace dorsal surface occasionally with reddish brown patches; thoracic sternites, pleon and lower surfaces of pereopods occasionally with scattered brown or gray spots; setae on pereopods generally brown (Figs. 6A, B; 8A, B). Size. Males 1.8×3.3–3.6× 8.3 mm; ovigerous females 1.9×3.9–4.2× 9.2 mm. Abnormalities. Three specimens [CBM-ZC 9135 (2.5× 4.7 mm), 15289 (2.6× 5.6 mm) and 15292 (2.7× 5.6 mm)] are androgynous in having male-like pleons (cf. Fig. 8B) with functionally fused pleomeres 4–6, which are proportionally slightly wider than in normal males, gonopores on the thoracic sternite 6, and pleomeres 2–5, of which the anterior two pairs are biramous and posterior two pairs are uniramous; the sterno-pleonal cavity is proportionally wider than in normal males, defined by less developed ridges; rudimentary press buttons are evident. The size of these androgynous specimens are included in the range of the adult size of the species (see above “Size”). Androgyny in the Brachyura is little known, but some examples have been reported in the pinnotherid Pinnotherinae De Haan, 1833 (e.g., Manning 1993, 1998; Ahyong and Ng 2008; Ahyong 2020), the varunid Pseudopinnixa Ortmann, 1894 (Komai & Konishi 2012), and the ocypodid Leptuca Bott, 1973 (Zou & Fingerman 2000), the potamid Geothelphusa Stimpson, 1858 (e.g. Takahashi et al. 2000), and portunid Catoptrus A. Milne-Edwards, 1870 (Naruse & Uyeno 2021). In the case of Indopinnixa haematosticta n. comb., there is no doubt that the observed androgyny represents an abnormality. Distribution and habitat. So far known only from Japan: Kanagawa Prefecture to Tanegashima Island in Ohsumi Islands, southern Kyushu (Pacific side) and Yamaguchi Prefecture (Sea of Japan side); intertidal to 50 m. Most specimens examined were extracted from sand substrates by using yabby pumps or shovels (see “Material examined”). One male specimen (CBM-ZC 15286; Ena Bay, Miura, Kanagawa Prefecture) was collected from a tube of terebellid worm, representing an example of possible association. Remarks. The female holotype of Indopinnixa haematosticta n. comb. is now in rather poor condition: the entire cephalothorax, pleon and appendages are decalcified; the right cheliped is missing; setae on appendages thickly bear mucus-like matter, sometimes making difficult to observe detailed structure of those appendages; in particular, the maxillipeds 3 are completely obscured, which is difficult to remove without much damage to the specimen. Fortunately, Sakai (1934, 1939, 1976) provided a figure of the maxilliped 3. The following features are still visible in the holotype: carapace broad (> 2.0 times as long as broad), with sharply delimited transverse carina, falling far short of lateral margins of carapace, on weakly elevated cardiac region (Fig. 7A); chela with lines of numerous setae on upper and lower margins and along mid-line of outer surface of palm (Fig. 7C); fixed finger of chela not deflexed, straight (Fig. 7C); cheliped dactylus nearly straight except for curved tip, shorter than palm (Fig. 7C); carpi of pereopods 2 and 3 each with sharply carinate extensor margin (Fig. 7D, E); propodi of pereopods 2 and 3 each with sharply carinate extensor and flexor margins (Fig. 7D, E); merus of pereopod 4 stout, 1.8 times as long as wide, posterior surface filled with dense plumose setae (Fig. 7F, G); pleomere 1 with fringe of short setae extending onto thoracic sternite 8 as transverse row (setae omitted in Fig. 7E, but see Fig. 6B for supplemental information). We identified the newly collected material from Japanese mainland used in this study based on these features. Yamauchi & Konishi (2005) failed to detect a sharply delimited transverse carina on the cardiac region of the carapace in the holotype, but we confi
Data for ''First simulations of day-to-day variability of mid-latitude sporadic E layer structures''
No full textOne file was added on July 21, 2020. (Caiondensity_average.nc)Two files were added on August 3, 2020. (ReadMe2_si_grl.pdf, S1.txt)The title was changed on August 3, 2020. (Before: Simulated Calcium Ion Density)One author was added on August 3, 2020. (Shinagawa Hiroyuki)ReadMe file was replaced on October 13, 2020.Two files were deleted on October 13, 2020. (ReadMe2_si_grl.pdf, S1.txt)Three files were added on October 13, 2020. (MeridionalWind_fig1.txt, VerticalWind_fig1.txt, ZonalWind_fig1.txt
Mid-Air Ultrasonic Stimulations of the Palm - The Influence of Frequency and Stimulus Duration on Perceived Intensity
No full textIt is known that the duration of a short stimulus affects the perceived intensity of both visual, auditory, and, vibrotactile events, but it is still unclear whether such a relationship also exists for mid-air ultrasonic inputs to the hand. Here we investigate this issue and show how the perceived intensity of focused ultrasonic stimulations of the palm is indeed systematically related to stimulus duration - a relationship that is, however, independent of modulation frequency. This is an important finding for the overall goal of providing perceptually stronger inputs and enlarging the repertoire of realistic mid-air haptic experiences.Human Information Communication Desig
Indopinnixa Manning & Morton 1987
No full textGenus Indopinnixa Manning & Morton, 1987 Indopinnixa Manning & Morton, 1987: 543.— Rahayu & Ng 2010: 59. Type species. Indopinnixa sipunculana Manning & Morton, 1987. Emended diagnosis. Carapace much wider than long, transversely elliptical; integument firm; front narrow, with shallow median groove; dorsal surface generally glabrous, sparsely punctate, regions poorly defined, sometimes with blunt or clearly demarcated transverse ridge across cardiac region, ridge not extending entirely across carapace; orbit broadly ovate, with wide inner hiatus partly occupied by basal article of antennal peduncle. Eyestalks very short, completely filling orbits. Antennular peduncles folded into wide fossae, separated by shallow median septum, under front. Maxilliped 3 with ischium and merus completely fused (= ischiomerus), narrow, subtrapezoidal; palp (carpus + propodus + dactylus) as long as or longer than ischiomerus; propodus and dactylus flattened, tongue-shaped; dactylus articulated to middle portion of flexor margin of propodus, far overreaching rounded distal margin of propodus. Chelipeds compressed, setose; palm with a longitudinal line of granules and setae along midline of outer surface; fingers slender, dactylus upper margin typically with row of long setae. Ambulatory pereopods (pereopods 2–5) relative lengths P4> P3 ≥ P2> P5; pereopod 4 heavy, merus particularly stout, marginally granulate or dentate. Male pleon constricted, with at least somites 5 and 6 functionally fused (sutures between somites may be discernible); no gonopodal plate developed on inner side; telson much wider than long, wider than pleomere 6. Female pleon consisting of six free somites, not concealing lateral parts of thoracic sternum. Male gonopod 1 tapering distally, but shape and setation of distal part variable according to species. Composition. Seven species (all from the Indo-West Pacific): Indopinnixa haematosticta (Sakai, 1934) n. comb., I. kasijani Rahayu & Ng, 2010, I. moosai Rahayu & Ng, 2010, I. mortoni Davie, 1992, I. oryza Naruse & Maenosono, 2012, I. shellorum Ng, 2014 and I. sipunculana (type species). Remarks. The monophyly of Pinnixa has been questioned (e.g., Rahayu & Ng 2010; Naruse & Maenosono 2012; Palacios Theil et al. 2016), and recently, Palacios Theil & Felder (2020) partially revised American species assigned to Pinnixa and allied genera based on molecular phylogenetic analysis in combination with morphological studies. As a result, Pinnixa was restricted to its type species P. cylindrica (Say, 1818), and the other 20 species reexamined were reassigned to Glassella Campos & Wicksten, 1997, Scleroplax Rathbun, 1894 and the three newly established genera, Rathbunixa Palacios Theil & Felder, 2020, Sayixa Palacios Theil & Felder, 2020 and Tubicolixa Palacios Theil & Felder, 2020. The generic placement of the seven Asian species (Pinnixa balanoglossana Sakai, 1934, P. banzu Komai, Nishi & Taru, 2014, P. haematosticta Sakai, 1934, P. lata Komatsu & Takeda, 2009, P. penultipedalis Stimpson, 1858, P. rathbuni Sakai, 1934, and P. tumida Stimpson, 1858), however, were not addressed. Manning & Morton (1987) distinguished Indopinnixa from Pinnixa s.l. primarily by the fusion of the male pleomeres 5 and 6, rather than all pleomeres been freely articulated in Pinnixa s.l. However, Naruse & Maenosono (2012) argued that species assigned to Pinnixa at the time exhibit various degree of fusion of the male pleomeres. The molecular phylogenetic analyses by Palacios Theil & Felder (2020) placed a clade including Indopinnixa kumejima and I. moosai in sister relation to a clade including some species of Pinnixa s.l. [P. abbotti Glassell, 1935, P. arenicola Rathbun, 1922, P. floridana Rathbun, 1918 Glassella costaricana (Wicksten, 1982), Laminapinnixa miamiensis McDermott, 2014, and Laminapinnixa faxoni (Rathbun, 1918)]. On the basis of the inferred phylogenetic pattern, Laminapinnixa McDermott, 2014 was synonymised with Glassella Campos & Wicksten, 1997 in spite of the considerable difference in the structure of the maxilliped 3; while Indopinnixa and Glassella were maintained as distinct genera for the time being. From the morphological perspective, species assigned to Indopinnixa and Glassella share the following features: at least pleomeres 4–6 are functionally fused, although sutures are sometimes evident on the outer surface; the telson does not taper, being wider than the narrowest portion of the pleomere 6; the maxilliped 3 dactylus is large and heavy, longer than the propodus; the external surface of the chela palm often bears longitudinal ridges or lines of granules on the midline; the pereopod 4 is very stout (cf. Manning & Morton 1987; Davie, 1992; Rahayu & Ng 2010; Naruse & Maenosono 2012; Ng 2014; Palacios Theil & Felder 2020; Felder & Palacios Theil 2020). Species assigned to Indopinnixa differ from those assigned to Glassella as diagnosed by Palacios Theil & Felder (2020) in the absence of a gonopodal plate developed on the inner side of the male pleon and the rather simple, generally tapering gonopod 1 (although the shape of the distal part is rather variable according to species). In species assigned to Glassella, all from the West Atlantic, including the Gulf of Mexico and the Caribbean Sea, the male pleon has a gonopodal plate or sheath extending between or against gonopods (cf. McDermott 2014; Palacios Theil & Felder 2020); and the male gonopod 1 is relatively stout, terminally forming sharp angle, spinose tip, or distally to laterally directed corneous filament. Differentiating characters among the genera of Pinnixinae Števčić, 2005 refer to Palacios Theil & Felder (2020). Our studies show that Pinnixa haematosticta agrees closely with Indopinnixa, and is in fact, very similar morphologically to I. kumejima. Here the generic diagnosis of Indopinnixa is emended, and Pinnixa haematosticta is transferred to Indopinnixa.Published as part of Komai, Tomoyuki, Naruse, Tohru, Yokooka, Hiroyuki, Taru, Masanori, Shimetsugu, Miho & Watanabe, Tetsuya, 2022, Redescription of Pinnixa haematosticta Sakai, 1934, its transfer to Indopinnixa Manning & Morton, 1987, and a reappraisal of Indopinnixa kumejima Naruse & Maenosono, 2012 (Decapoda: Brachyura: Pinnotheridae), pp. 361-389 in Zootaxa 5100 (3) on pages 364-365, DOI: 10.11646/zootaxa.5100.3.3, http://zenodo.org/record/620160
Range extension of the sesarmid crab Clistocoeloma villosum along the eastern Pacific coast of the Izu Peninsula, Japan
No full textRFLNA遺伝子のフレームシフト変異をホモ接合性に認めた典型的な脊椎手根骨足根骨癒合症の一例
No full textSpondylocarpotarsal synostosis syndrome, a rare syndromic skeletal disorder characterized by disrupted vertebral segmentation with vertebral fusion, scoliosis, short stature, and carpal/tarsal synostosis, has been associated with biallelic truncating mutations in the filamin B gene or monoallelic mutations in the myosin heavy chain 3 gene. We herein report the case of a patient with a typical phenotype of spondylocarpotarsal synostosis syndrome who had a homozygous frameshift mutation in the refilin A gene (RFLNA) [c.241delC, p.(Leu81Cysfs*111)], which encodes one of the filamin-binding proteins. Refilins, filamins, and myosins play critical roles in forming perinuclear actin caps, which change the nuclear morphology during cell migration and differentiation. The present study implies that RFLNA is an additional causative gene for spondylocarpotarsal synostosis syndrome in humans and a defect in forming actin bundles and perinuclear actin caps may be a critical mechanism for the development of spondylocarpotarsal synostosis syndrome.長崎大学学位論文 学位記番号:博(医歯薬)甲第1200号 学位授与年月日:令和2年3月19日Author: Hitomi Shimizu, Satoshi Watanabe, Akira Kinoshita, Hiroyuki Mishima, Gen Nishimura, Hiroyuki Moriuchi, Koh-ichiro Yoshiura & Sumito DatekiCitation: Journal of Human Genetics, 64(5), pp.467-471, 201
Effects of rewarming therapies on outcomes in accidental hypothermia: A secondary analysis of a multicenter prospective study
No full text弘前大学博士（医学）Author(s): Kana Sugiyama, Osamu Nomura, Jin Irie, Yoshiya Ishizawa, Shuhei Takauji, Mineji Hayakawa, Yoshinori Tamada, Hiroyuki Hanad
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