60,887 research outputs found
Four and a half LIM protein 1C (FHL1C)
No full textFour-and-a-half LIM domain protein 1 isoform A (FHL1A) is predominantly expressed in skeletal and cardiac muscle. Mutations in the FHL1 gene are causative for several types of hereditary myopathies including X-linked myopathy with postural muscle atrophy (XMPMA). We here studied myoblasts from XMPMA patients. We found that functional FHL1A protein is completely absent in patient myoblasts. In parallel, expression of FHL1C is either unaffected or increased. Furthermore, a decreased proliferation rate of XMPMA myoblasts compared to controls was observed but an increased number of XMPMA myoblasts was found in the G(0)/G(1) phase. Furthermore, low expression of K(v1.5), a voltage-gated potassium channel known to alter myoblast proliferation during the G(1) phase and to control repolarization of action potential, was detected. In order to substantiate a possible relation between K(v1.5) and FHL1C, a pull-down assay was performed. A physical and direct interaction of both proteins was observed in vitro. In addition, confocal microscopy revealed substantial colocalization of FHL1C and K(v1.5) within atrial cells, supporting a possible interaction between both proteins in vivo. Two-electrode voltage clamp experiments demonstrated that coexpression of K(v1.5) with FHL1C in Xenopus laevis oocytes markedly reduced K(+) currents when compared to oocytes expressing K(v1.5) only. We here present the first evidence on a biological relevance of FHL1C
Multiple functions of LIM domain-binding CLIM/NLI/Ldb cofactors during zebrafish development
No full textThe crucial involvement of CLIM/NLI/Ldb cofactors for the exertion of the biological activity of LIM homeodomain transcription factors (LIM-HD) has been demonstrated. In this paper we show that CLIM cofactors are widely expressed during zebrafish development with high protein levels in specific neuronal cell types where LIM-HD proteins of the Isl class are synthesized. The overexpression of a dominant-negative CLIM molecule (DN-CLIM) that contains the LIM interaction domain (LID) during early developmental stages of zebrafish embryos results in an impairment of eye and midbrain-hindbrain boundary (MHB) development and disturbances in the formation of the anterior midline. On a cellular level we show that the outgrowth of peripheral but not central axons from Rohon Beard (RB) and trigeminal sensory neurons is inhibited by DN-CLIM overexpression. We demonstrate a further critical role of CLIM cofactors for axonal outgrowth of motor neurons. Additionally, DN-CLIM overexpression causes an increase of Isl-protein expression levels in specific neuronal cell types, likely due to a protection of the DN-CLIM/LIM-HD complex from proteasomal degradation. Our results demonstrate multiple roles of the CLIM cofactor family for the development of entire organs, axonal outgrowth of specific neurons and protein expression levels
A comment on "Intergenerational equity: sup, inf, lim sup, and lim inf"
No full textWe reexamine the analysis of Chambers (Social Choice and Welfare, 2009), that produces a characterization of a family of social welfare functions in the context of intergenerational equity: namely, those that coincide with either the sup, inf, lim sup, or lim inf rule. Reinforcement, ordinal covariance, and monotonicity jointly identify such class of rules. We show that the addition of a suitable axiom to this three properties permits to characterize each particular rule. A discussion of the respective distinctive properties is provided.Social welfare function; Intergenerational equity; Lim sup ; Lim inf
Bluff bodies in deep turbulent boundary layers: Reynolds-number issues
No full textIt is generally assumed that flows around wall-mounted sharp-edged bluff bodies
submerged in thick turbulent boundary layers are essentially independent of the
Reynolds number Re, provided that this exceeds some (2–3) × 104. (Re is based on
the body height and upstream velocity at that height.) This is a particularization of
the general principle of Reynolds-number similarity and it has important implications,
most notably that it allows model scale testing in wind tunnels of, for example,
atmospheric flows around buildings. A significant part of the literature on wind
engineering thus describes work which implicitly rests on the validity of this
assumption. This paper presents new wind-tunnel data obtained in the ‘classical’ case
of thick fully turbulent boundary-layer flow over a surface-mounted cube, covering an
Re range of well over an order of magnitude (that is, a factor of 22). The results are
also compared with new field data, providing a further order of magnitude increase in
Re. It is demonstrated that if on the one hand the flow around the obstacle does not
contain strong concentrated-vortex motions (like the delta-wing-type motions present
for a cube oriented at 45? to the oncoming flow), Re effects only appear on fluctuating
quantities such as the r.m.s. fluctuating surface pressures. If, on the other hand, the
flow is characterized by the presence of such vortex motions, Re effects are significant
even on mean-flow quantities such as the mean surface pressures or the mean velocities
near the surfaces. It is thus concluded that although, in certain circumstances and for
some quantities, the Reynolds-number-independency assumption is valid, there are
other important quantities and circumstances for which it is not
Platyrrhinus guianensis Velazco & Lim, 2014, new species
No full textPlatyrrhinus guianensis new species Guianan Broad-nosed Bat Figures 4–7 P [latyrrhinus]. helleri: Lim, 1993: 162 (part) Platyrrhinus helleri: Smith and Kerry, 1996: 932 (part) Platyrrhinus helleri: Lim and Engstrom, 2000: 121 P [latyrrhinus]. helleri: Lim and Engstrom, 2001 a: 632 (part) Platyrrhinus helleri: Lim and Engstrom, 2001 b: 664 (part) Platyrrhinus helleri: Engstrom and Lim, 2002: 364 (part) Platyrrhinus helleri: Lim and Norman, 2002: 54 P [latyrrhinus]. helleri: Lim et al., 2002: 1239 (part) Platyrrhinus helleri: Lim and Engstrom, 2005: 77 (part) Platyrrhinus helleri: Lim et al., 2005 a: 244 (part) Platyrrhinus helleri: Lim et al., 2005 b: 87 (part) Platyrrhinus helleri: Clare et al., 2007: 187 (part) Platyrrhinus helleri: Borisenko et al., 2008: 475 (part) Platyrrhinus helleri: Lim, 2009: 45 (part) P [latyrrhinus]. recifinus: Velazco, 2009: 259 (part) Platyrrhinus recifinus: Tavares and Velazco, 2010: 119 (part) Platyrrhinus helleri: Clare et al., 2011: 8 (part) Platyrrhinus helleri: Clare, 2011: 4 (part) Platyrrhinus helleri: Lim, 2012: 253 (part) Platyrrhinus helleri: Lim and Tavares, 2012: 115 (part) Holotype. Dried skin, skull and skeleton of an adult pregnant female, Royal Ontario Museum (ROM) number 113465, obtained 20 September 2001 by Burton K. Lim and Zacharias Norman (original field number F 50445). The skin, skull, and skeleton are in good condition. Frozen tissues are deposited at the Royal Ontario Museum (F 50445). Type locality. Pobawau Creek mouth, 100 m; Upper Takutu-Upper Essequibo; Guyana, 3 ° 16 ’ 3.1 ”N, 58 ° 46 ’ 42.7 ”W (Fig. 3). Paratypes. The skin, skull, and skeleton of an adult male (ROM 108487) caught on 8 October 1997 at 38 mi Camp, 35 km SW Kurupukari, 100 m, Iwokrama Forest, Potaro-Siparuni, Guyana, 4 ° 22 ’W, 58 ° 51 ’W; one skin and skull of an adult male (ROM 114070) caught on 16 April 2002 and one skin, skull, and skeleton of an adult pregnant female (ROM 113991) caught on 13 April 2002 at Brownsberg Nature Park headquarters, 500 m, Brokopondo, Suriname, 4 ° 57 ’N, 55 ° 11 ’W; and the skin and skull of an adult male (ROM 114195) caught on 21 April 2002 at Km 2.4 Wittie Kreek trail, 300 m, Brownsberg Nature Park, Brokopondo, Suriname, 4 ° 56 ’N, 55 ° 10 ’W. The holotype and 4 paratypes, along with 31 other specimens from the known distributional range, are listed in Appendix 1 (Fig. 3). Measurements of each specimen of the type series of P. guianensis are provided in Table 4. Distribution. Platyrrhinus guianensis is known from Guyana and Suriname (Fig. 3). Etymology. The species name is derived from the Latin description of its endemic distribution in the Guiana region of South America. Diagnosis. Platyrrhinus guianensis is distinguished from its congeners by a combination of external and craniodental characteristics. The ventral fur is dark gray; ventral fur unicolor; dorsal stripe wide and brilliant white; fringe of hair along margin of uropatagium long, conspicuously dense, and pale yellow. The skull of P. guianensis lacks a fossa on the squamosal root of the zygomatic arch. Dentally, two stylar cuspules are present on the posterior cristid of P 4; and one stylid cuspulid on the anterior cristid of p 4. Description. Platyrrhinus guianensis is a small Platyrrhinus (FA 37–41 mm) distinguished from its sister species P. recifinus by its smaller size and shorter skull (Table 5; Velazco & Gardner 2009, Table 2–4 and 7). However, measurements of P. guianensis overlap with P. angustirostris, P. brachycephalus, P. fusciventris, P. helleri, P. i n c a r u m, and P. matapalensis (Tables 4 –5). Dorsal fur mostly dark brown, but paler on the upper dorsum; dorsal fur is bicolored with darker tips; facial stripes wide and white; dorsal stripe brilliant white; ventral fur dark gray, individual hairs unicolored; pinnae have well-marked fold lines; tragus and anterior and posterior rims of pinnae bright yellow (Fig. 4); lateral borders of the proximal half of the noseleaf and borders of the horseshoe yellow; inferior border of the horseshoe completely free of upper lip; posterior margin of uropatagium has the shape of an inverted ‘U’; hair on upper surface of feet brown, long and dense (Fig. 5); fringe of hair along the trailing margin of uropatagium long, conspicuously dense, and pale yellow; metacarpal III longer than metacarpal V. Rostrum is slender; has a well developed anterior notch in the nasals; postorbital processes moderately developed; paraoccipital processes poorly developed; two infraorbital foramina present; posterior border of hard palate ‘V’-shaped (Fig. 6); fossa on the squamosal root of the zygomatic arch absent; and paraoccipital and paracondylar processes poorly developed. Upper inner incisors bilobed and convergent, not in contact, and tips extend below level of cingula of upper canines; upper outer incisors monolobate; two stylar cuspules on posterior cristid of P 4; hypoconal basin fossa of P 4 shallow; M 1 parastyle present; M 1 mesostyle absent; M 1 metacone divided in two cones; M 1 metacone labial cingulum present; stylar cuspule absent on lingual cingulum of M 1 metacone; sulcus on posterior cristid of paracone joined to cingulum of lingual face of metacone on M 1; M 1 metastyle present; M 1 protocone well developed; M 2 parastyle present; labial cingulum present on M 2 paracone; stylar cuspule on lingual face of M 2 paracone absent; M 2 metastyle present; stylar cuspule absent on lingual face of M 2 metacone; lingual cingulum of the M 2 metacone not extending to the paracone; developed M 2 hypoconal basin; M 3 minute; labial and lingual cingulids on p 4; one stylid cuspulid on anterior cristid of p 4; two stylid cuspulids on posterior cristid of p 4; m 1 paraconid poorly developed; labial and lingual cingulids present on m 1; stylid cuspulid present on anterior cristid of m 1 protoconid; m 1 metaconid well developed; m 2 hypoconid absent; stylid cuspulid between the metaconid and protoconid poorly developed on m 2; labial and lingual cingulids present on m 2. Comparisons. Platyrrhinus guianensis can be confused with P. angustirostris, P. brachycephalus, P. fusciventris, P. he l l e r i, P. i nc a r u m, and P. matapalensis because their external and cranial measurements overlap (Table 3–4). But it can be easily distinguished from P. brachycephalus and P. matapalensis by the presence of one accessory cuspulid on the anterolingual cristid of p 4 (Fig. 7) (cuspulid lacking in P. matapalensis and two accessory cuspulids present in P. brachycephalus; Velazco 2005, fig. 27). Therefore, the following comparisons focus on differentiating P. guianensis from P. angustirostris, P. fusciventris, P. helleri, and P. incarum. Externally, ventral fur is dark gray in P. guianensis and P. angustirostris (brownish gray in P. i n c ar u m; pale gray in P. h el l e r i; brown in P. fusciventris); ventral fur unicolored in P. guianensis, P. angustirostris, P. fusciventris, and P. h el l e r i (bicolored in P. i nc a r u m); dorsal stripe wide and brilliant white in P. guianensis and P. he l l e r i (conspicuous but narrow in P. angustirostris, P. fusciventris, and P. incarum); tragus and anterior and posterior rims of pinnae bright yellow in P. guianensis, P. fusciventris, and P. helleri (whitish in P. angustirostris and P. incarum); lateral borders of the proximal half of the noseleaf and borders of the horseshoe yellow in P. guianensis, P. fusciventris, and P. he l l e r i (whitish in P. angustirostris and P. i n c ar um); posterior margin of uropatagium with a shape of an inverted ‘U’ in P. guianensis, P. angustirostris, and P. i n c ar u m (‘V’ shaped in P. fusciventris and P. helleri); fringe of hair along margin of uropatagium long, conspicuously dense, and pale yellow in P. guianensis (long, dense, and pale brown in P. helleri; long, dense, and whitish in P. fusciventris and P. i nc a r u m; short, dense, and pale brown in P. angustirostris); hair on the upper surface of feet brown, long and dense in P. guianensis, P. angustirostris, and P. i n c a r um (short and intermediate in density in P. fusciventris and P. hell eri); metacarpal III longer than metacarpal V in P. guianensis, P. angustirostris, and P. i n c a r um (metacarpals III and V subequal in P. fusciventris and P. he l l e r i). Cranially, there is a ‘V’-shaped posterior border of the hard palate in P. guianensis, P. angustirostris, P. hel leri, and P. i n c ar u m (‘V’- or ‘U’-shaped in P. fusciventris); fossa on the squamosal root of the zygomatic arch absent in P. guianensis, P. helleri, and P. i ncarum (shallow in P. angustirostris and P. fusciventris). Dentally, there are two stylar cuspules on posterior cristid of P 4 in P. guianensis, P. fusciventris, P. helleri, and P. i nc a r u m (three in P. angustirostris); stylar cuspule on lingual face of M 2 paracone absent in P. guianensis, P. angustirostris, and P. fusciventris (one stylar cuspule in P. he l l e r i and P. incarum); M 3 minute in P. guianensis and P. i n ca r u m (larger in P. h el l e r i, P. angustirostris, and P. fusciventris); one stylid cuspulid on the anterior cristid of p 4 in P. guianensis, P. fusciventris, and P. helleri (one or two in P. i n ca r u m and P. angustirostris); tall m 2 protoconid in P. guianensis, P. angustirostris, P. fusciventris, P. i n c a r um (Fig. 7) (shorter in P. helleri); hypoconid lacking on m 2 in P. guianensis, P. angustirostris, P. fusciventris, and P. helleri (poorly developed in P. i n c a r um); poorly developed stylid cuspulid between the metaconid and protoconid on m 2 in P. guianensis, P. fusciventris, and P. helleri (well developed in P. i ncarum and P. angustirostris). Natural history. Platyrrhinus guianensis has been documented from an elevational range of 60 to 500 m and is found primarily in rainforest (n= 33), but 3 individuals were netted in savanna. Of the 36 specimens examined, 16 are males and 20 females. Testes size (length by width in mm) ranged from 3 by 2 to 5 by 4. From 12 January to 9 February 2006, 8 of 10 females were pregnant with crown-rump (CR) measurements ranging from 4 to 13 mm. A female was pregnant on 13 April 2002 and another on 27 July 2009 with CR of 13 mm and 4 mm, respectively. Three females were pregnant on 20 and 21 September 2001 with CR ranging from 18 to 21 mm. A non-pregnant female was collected on 24 October 1997. A female had an embryo with CR of 26 mm collected on 31 October 2005. Two non-pregnant lactating females were caught on 8 and 11 November 1999 and one non-pregnant female was caught on 19 November 1997.Published as part of Velazco, Paúl M. & Lim, Burton K., 2014, A new species of broad-nosed bat Platyrrhinus Saussure, 1860 (Chiroptera: Phyllostomidae) from the Guianan Shield, pp. 175-193 in Zootaxa 3796 (1) on pages 181-189, DOI: 10.11646/zootaxa.3796.1.9, http://zenodo.org/record/22516
A new species of swamp-dwelling skink (Tytthoscincus) from Singapore and Peninsular Malaysia
No full textGrismer, L. Lee, Wood, Perry L., Jr, Lim, Kelvin K. P., Liang, Lim J. (2017): A new species of swamp-dwelling skink (Tytthoscincus) from Singapore and Peninsular Malaysia. Raffles Bulletin of Zoology 65: 574-584, DOI: 10.5281/zenodo.535801
Fig. 8 in Two new species of Barbodes from the Malay Peninsula and comments on 'cryptic species' in the B. binotatus group (Teleostei: Cyprinidae)
No full textFig. 8. The forest stream (a) inhabited by Barbodes sellifer, new species, in the type locality, Nee Soon swamp-forest in Singapore; and a view from the surface (b) showing a congregation of many individuals of B. sellifer (with the distinct black subdorsal blotch) with a few Rasbora elegans (with the two black spots on the side). (Photographs by K. K. P. Lim, March 2005).Published as part of Kottelat, Maurice & Lim, Kelvin K. P., 2021, Two new species of Barbodes from the Malay Peninsula and comments on 'cryptic species' in the B. binotatus group (Teleostei: Cyprinidae), pp. 522-540 in Raffles Bulletin of Zoology 69 on page 530, DOI: 10.26107/RBZ-2021-0069, http://zenodo.org/record/717447
Ptyas carinata
No full textPtyas carinata (Ģnther, 1858b) — Native. Zaocys carinatus Ģnther, 1864: 256 [nec Coryphodon carinatus Ģnther, 1858b: 112–113]. Lectotype: BMNH 1946.1.11.35, designated by Ģnther (1864: 256). Type locality: “Borneo [and] Chusan [and] Khasya [and] Sikkim [and] Affghanistan [sic]” (= Borneo; Zhoushan, China; Kasya, Kushinagar, India; Sikkim, India, and; Afghanistan); later restricted to “Borneo” via lectotype designation. Keeled Rat Snake (Figure 19H; Mandai Track 15) Singapore records. Zaocys carinatus — Boulenger, 1893: 377.— Flower, 1896: 881.— Hall, 1988: 19.— Flower, 1899: 666.— Ridley, 1899: 206.— Boulenger, 1912: 135.— Hanitsch, 1912b: 16.—M.A. Smith, 1916b: 160.— de Rooij, 1917: 73.—Sworder, 1923: 62.— de Haas, 1950: 537.—K. Lim & F. Lim, 1988a: 27 (Sime Road [SRF]).—K. Lim & F. Lim, 1988b: 49 (Singapore Zoo).—K. Lim & F. Lim, 1988c: 74 (Mandai Lake Road).—K. Lim & F. Lim, 1989: 3 (Boundary Path [BTNR]).—F.L.K. Lim & M.T.- M. Lee, 1989: 116.—K. Lim, 1990a: 7 (Nee Soon Swamp Forest; Sime Road Forest).—K.K.P. Lim & L.M. Chou, 1990: 54.—F.L.K. Lim, 1991: 58.—L.M. Chou et al., 1994: 105.—R. Subaraj, 1995: 101. Ptyas carinatus —Taylor, 1965: 736.—K.K.P. Lim & F.L.K. Lim, 1992: 56, 145.—K.K.P. Lim, 1993a: 3 (Catchment Path [BTNR]; Rifle Range Road).—R. Subaraj et al., 1995: 2 (MacRitchie North [MNF]).—K. Lim, 1995: 15 (Bukit Timah Nature Reserve).— David & Vogel, 1996: 105.—K.K.P. Lim, 1996: 51.—R.C.H. Teo & Rajathurai, 1997: 383 (Bukit Timah [BTNR]).—Chan-ard et al., 1999: 35.— Iskandar & Colijn, 2001: 79.—K.P. Lim & F.L.K. Lim, 2002: 146.— Fry et al., 2003b: 2050. Zoacys [sic] carinatus —L.M. Chou, 1995: 148. Zaocys carinata — Manthey & Grossmann, 1997: 402. Ptyas carinata — Cox et al., 1998: 55.—N. Baker & K.P. Lim, 2008: 107, 161.— Das, 2010: 298.—L.L. Grismer, 2011a: 211.—P.K.L. Ng et al., 2011: 273.—N. Baker & K.P. Lim, 2012: 107, 161.— Das, 2012a: 63.—Wallach et al., 2014: 615.—Chan-ard et al., 2015: 171.— de Lang, 2017: 181.— Das, 2018: 74.—R.C.H. Teo & Thomas, 2019: 164, 181 (Bukit Timah Nature Reserve).— Charlton, 2020: 190–191 (Dairy Farm Nature Park).— Dubois & David, 2020: 112.—C.C. Ong & C. Yeong, 2020: 145 (Thomson Nature Park). Remarks. From early on, the occurrence of P. carinata in Singapore was known only from Boulenger (1893) who first reported it based on a specimen deposited at NHMUK collected by Dennys, and by Hanitsch (1898) who noted that this species is represented in the the Raffles Museum collection. However, the LKCNHM only has specimens from 1899, 1922, 1926, 1933, 1986, 1987, and two from 2008. After Hanitsch (1898), P. carinata was only next reported 90 years later (Table 2) from a live specimen detected at SRF on 26 June 1988 (Lim & Lim 1988a). That same year, another was seen at Singapore Zoo on 6 September 1988 (Lim & Lim 1988b), and on Mandai Lake Road on 23 December 1988 (Lim & Lim 1988c). Subsequent observations include a mating pair at BTNR on 12 February 1989 (Lim & Lim 1989), two seen at NSSF and SRF (Lim 1990a), two seen at BTNR and RRR (Lim 1993a), one observed eating a D. caudolineatus at MNF on 8 May 1994 (Subaraj et al. 1995), a roadkill at BTNR on October 1995 (Lim 1995), and Teo & Rajathurai (1997) noted a total of 21 records during their survey, some which likely include the antecedent records. Nowadays, P. carinata is considered common (Teo & Rajathurai 1997; Baker & Lim 2012), but surprisingly, no current records have been reported aside from one seen at BTNR (Teo & Thomas 2019) and one observed eating an O. octolineatus at TNP on 6 July 2020 (Ong & Yeong 2020). LKCNHM has two specimens from 2008, Charlton (2020) published a photograph of one from DFNP, and the individual in Figure 19H was seen at Mandai Track 15 on 21 October 2018 (I.S. Law pers. comm.). Occurrence. Restricted to CNR and surrounding Nature Parks and forests. Uncommon. Singapore conservation status. Vulnerable. Conservation priority. Highest. IUCN conservation status. Least Concern [2012]. LKCNHM & NHMUK Museum specimens. Singapore (no locality): BMNH 1880.9.10.2 (no date); Bukit Timah : ZRC.2.4555 (Feb-1922); Bukit Timah Nature Reserve : ZRC.2.6169 (no date); Hindhede Drive : ZRC.2.2305 (21-Feb-1986), ZRC.2.2306 (08-Oct-1987); Impounding [MacRitchie] Reservoir : ZRC.2.4551 (1899); Old Upper Thomson Road : ZRC.2.6735 (22-Jul-2008); Singapore Golf Club [SICC] : ZRC.2.4549 (21-Dec-1933); Thomson Road Reservoir [MR] : ZRC.2.4547 (May-1926); Upper Seletar Reservoir Road : ZRC.2.6713 (11-Jul-2008). Additional Singapore museum specimens. Singapore (no locality): AMNH. Singapore localities. Bukit Timah (not specified)—Bukit Timah Nature Reserve—Dairy Farm Nature Park— Hindhede Drive—MacRitchie North Forest—MacRitchie Reservoir—Mandai Lake Road—Mandai Track 15—Nee Soon Swamp Forest—Old Upper Thomson Road—Rifle Range Road—Sime Road Forest— Singapore Island Country Club— Singapore Zoo—Thomson Nature Park—Upper Seletar Reservoir Road.Published as part of Figueroa, Alex, Low, Martyn E. Y. & Lim, Kelvin K. P., 2023, Singapore's herpetofauna: updated and annotated checklist, history, conservation, and distribution, pp. 1-378 in Zootaxa 5287 (1) on pages 172-173, DOI: 10.11646/zootaxa.5287.1.1, http://zenodo.org/record/796031
Study of the p–p–K + and p–p–K - dynamics using the femtoscopy technique
No full textThe interactions of kaons (K) and antikaons (K ̄) with few nucleons (N) were studied so far using kaonic atom data and measurements of kaon production and interaction yields in nuclei. Some details of the three-body KNN and K ̄ NN dynamics are still not well understood, mainly due to the overlap with multi-nucleon interactions in nuclei. An alternative method to probe the dynamics of three-body systems with kaons is to study the final state interaction within triplet of particles emitted in pp collisions at the Large Hadron Collider, which are free from effects due to the presence of bound nucleons. This Letter reports the first femtoscopic study of p–p–K + and p–p–K - correlations measured in high-multiplicity pp collisions at s = 13 TeV by the ALICE Collaboration. The analysis shows that the measured p–p–K + and p–p–K - correlation functions can be interpreted in terms of pairwise interactions in the triplets, indicating that the dynamics of such systems is dominated by the two-body interactions without significant contributions from three-body effects or bound states
Pseudomystus rugosus
No full textP. rugosus: BMNH 1893.3.6.172, holotype, 103.1 mm SL; Borneo: Sarawak, Poeh.Published as part of Heok Hee Ng & Kelvin K. P. Lim, 2005, The identity of Pseudomystus moeschii (Boulenger, 1890), with the description of two new species of bagrid catfishes from Southeast Asia (Teleostei: Bagridae)., pp. 1-18 in Zootaxa 851 on page 1
- …
