29 research outputs found

    WONG, K.J.H., SHIH, H.-T. & CHAN, B.K.K. (2012) The ghost crab Ocypode mortoni George, 1982 (Crustacea: Decapoda: Ocypodidae): redescription, distribution at its type locality, and the phylogeny of East Asian Ocypode species. Zootaxa, 3550, 71-87.

    No full text
    H.-T (2013): WONG, K.J.H., SHIH, H.-T. & CHAN, B.K.K. (2012) The ghost crab Ocypode mortoni George, 1982 (Crustacea: Decapoda: Ocypodidae): redescription, distribution at its type locality, and the phylogeny of East Asian Ocypode species. Zootaxa, 3550, 71-87. Zootaxa 3626 (2): 300-300, DOI: http://dx.doi.org/10.11646/zootaxa.3626.2.

    Trevathana longidonta Chan & Chen & Achituv & Lin 2017, sp. nov.

    No full text
    Trevathana longidonta sp. nov. HTTP://zOOBANK.ORG/URN: LSID:zOOBANK.ORG:AcT:5811F4F9-C0F4-4506-B115-9472E746F279 FIGUReS 2G H; 23–30 Trevathana sp. nov. 3. Chan et al., 2013: 338, figs. 299–307. Material examined. HOLOTyPe: ASIZCR000359, LOBSTeR CAVe, SIAO-LIU-QIAO ISLAND, TAIWAN (22o20.41’N, 120o23.18’E, DePTH 10M), AUGUST 2010, cOLL. B.K.K. CHAN, ON cORAL Favites abdita (ELLIS & SOLANDeR, 1786). PARATyPeS: ASIZCR000360, DONGSHA ATOLL (20°41.478 N, 116°45.103 E), TAIWAN, MAy 2014, cOLL. P.C. TSAI. ON cORAL Favites abdita. ASIZCR000361, DATA SAMe AS ASIZCR000360. ASIZCR000227, DATA SAMe AS ASIZCR000359. OTHeR MATeRIALS: CEL-GI-172-1, GeNeRAL ROcK, GReeN ISLAND, TAIWAN, AUGUST 2010, cOLL. B.K.K. CHAN, ON FAVIIDAe (cORAL SPecIMeN TOO fRAGMeNTeD TO IDeNTIfy). CEL-TI- 11-1, TURTLe TAIL, KUeI SHAN ISLAND, TAIWAN, OcTOBeR 2010, cOLL. B.K.K. CHAN, ON cORAL Pavona venosa (EHReNBeRG, 1834), CEL-TI- 11-3, CEL-TI- 11-4 AND CEL-TI- 11-5, DATA SAMe AS CEL-TI- 11-1. CEL-KT-85-1, NANWAN, KeNTING, PINGTUNG COUNTy, TAIWAN, NOVeMBeR 2010, cOLL. B.K.K. CHAN, ON cORAL Favites abdita. CEL-DSA-6-1, DONGSHA ATOLL (20°41.478 N, 116°45.103 E), MAy 2014, cOLL. H.N. CHeN, P.C. TSAI, H.C. LIN, ON cORAL Favites abdita. CEL-DSA-54-5 DATA SAMe AS CEL-DSA-6-1. Diagnosis. ScUTAL WIDTH 4 TIMeS LONGeR THAN HeIGHT. OccLUDeNT MARGIN SLIGHTLy cURVeD. MeDIAN cLOSeD fURROW STRAIGHT, ABOUT 7/8 LeNGTH Of ScUTUM. ARTIcULAR MARGIN Of ScUTUM WITH INTeRLOcKING TOOTH, TOOTH NARROW, WIDTH ABOUT 1/2 Of ARTIcULAR MARGIN. ADDUcTOR PLATe ABSeNT. TeRGUM TRIANGULAR, BASAL MARGIN LONGeR THAN ScUTAL AND OccULDeNT MARGINS. INTeRNALLy, BASe Of TeRGUM WITH LONG, ROD-SHAPeD TOOTH, TOOTH eXTeNDING BeyOND cARINAL MARGIN. SPUR INDISTINcT. Description. SHeLL OVAL, cOVeReD By cORAL WHeN ALIVe (FIG. 2G, H). SHeLL (7.6 MM BD HOLOTyPe), fLAT, eLLIPTIcAL, PLATeS fUSeD, WHITe (AfTeR cLeANING AND PReSeRVATION), WITH SMALL PROjecTIONS ROUGHLy ARRANGeD ON SURfAce (FIG. 23A). CIRcUMfeReNce Of BASe Of SHeLL WITH 37 SHORT PROjecTIONS, PROjecTIONS MARGIN SeRRATeD (FIG. 23B). ORIfIce eLLIPTIcAL, ROSTRO-cARINAL AXIS ABOUT 1/3 Of BASAL ROSTRO-cARINAL DIAMeTeR Of SHeLL. ScUTUM AND TeRGUM WHITe, SePARATeD (FIG. 23C–G). ScUTUM TRANSVeRSALLy eLONGATeD, TeRGAL MARGIN 4 TIMeS LONGeR THAN OccLUDeNT MARGIN. OccLUDeNT MARGIN SLIGHTLy cURVeD, eXTeRNAL SURfAce Of ScUTUM WITH STRAIGHT MeDIAN fURROW cLOSeD, ABOUT 7/8 TOTAL LeNGTH Of ScUTUM. ARTIcULAR MARGIN WITH NARROW, SeMIcIRcULAR, INTeRLOcKING TOOTH, WIDTH Of TOOTH ABOUT 1/2 Of ARTIcULAR MARGIN, GROWTH LINeS ON TOOTH (FIG. 23G). ADDUcTOR PLATe ABSeNT (FIG. 23C). TeRGUM TRIANGULAR (FIG. 23E, F), WITH BASAL MARGIN SHORTeR THAN cARINAL AND ScUTAL MARGINS, SPUR LOW, ScUTAL MARGIN SLIGHTLy cONcAVe, NOTcHeD; INNeR SIDe Of ScUTAL MARGIN WITH SeMIcIRcULAR DePReSSION AccOMMODATING INTeRLOcKING TOOTH Of ScUTUM (FIG. 23F). INTeRNAL SURfAce Of TeRGUM WITH POINTeD, INWARD PROjecTING TOOTH LOcATeD ON SPUR (FIG. 23F), TOOTH eXTeNDING BeyOND cARINAL MARGIN. MAXILLA SUBTRIANGULAR, BILOBeD (FIG. 24A), WITH SIMPLe SeTAe DISTALLy (FIG. 24B),SeRRULATe SeTAe ON INTeRIOR MARGIN (FIG. 24C). MAXILLULe WITH cUTTING eDGe STRAIGHT, WITHOUT NOTcH, BeARING ROW Of 11 OR 12 SPINeS (cOUNTS fROM 4 SPecIMeNS, FIG. 24D, F–H). UPPeR AND LOWeR MARGINS WITH LONG, SIMPLe SeTAe. (FIG. 24E). MANDIBLe WITH 4 OR 5 TeeTH, eXcLUDING INfeRIOR ANGLe (cOUNTS fROM 4 SPecIMeNS, FIG. 25A, D, F, H). SecOND TO fOURTH TeeTH BIDeNTATe (FIG. 25B, D, F), UPPeR 3 TeeTH OccUPyING MORe THAN 2/3 LeNGTH Of cUTTING eDGe, LOWeR MARGIN SHORT, INfeRIOR ANGLe WITH SMALL SeTAe (FIG 25C, E, G). MANDIBULAR PALP OVAL, DISTAL eND ROUNDeD (FIG. 26A), DISTAL (FIG. 26B) AND INTeRIOR MARGINS WITH SeRRULATe SeTAe (FIG. 26C). LABRUM BILOBeD, WITH V-SHAPeD NOTcH SePARATING 2 LOBeS, BeARING 1–3 SHARP TeeTH ON eAcH LOBe (cOUNTS fROM 3 SPecIMeNS, FIG. 26D–H). CIRRUS I WITH RAMI UNeqUAL, ANTeRIOR RAMUS LONG, SLeNDeR, 9 SeGMeNTeD (FIGS. 27A, 28A), POSTeRIOR RAMUS 6 SeGMeNTeD, BeARING SeRRULATe SeTAe (FIG. 28A–D). CIRRUS II WITH RAMI SLIGHTLy UNeqUAL, ANTeRIOR RAMUS 7 SeGMeNTeD, POSTeRIOR RAMUS 6 SeGMeNTeD (FIGS. 27B, 28E), WITH SeRRULATe SeTAe (FIG. 28E, F, G, H). CIRRUS III WITH ANTeRIOR RAMUS SLIGHTLy LONGeR THAN POSTeRIOR RAMUS, 7 AND 6 SeGMeNTS ReSPecTIVeLy (FIGS. 27C, 29A), WITH SeRRULATe SeTAe (FIG. 29B– D). POSTeRIO-LATeRAL SIDe Of POSTeRIOR RAMUS Of cIRRUS III BeARING cONIcAL SPINeS (FIG. 29B). CIRRI IV–VI WITH LONG, SLeNDeR, RAMI Of SIMILAR LeNGTHS (FIGS. 27D–F, 29E–H, 30A–F). CIRRUS IV WITH ANTeRIOR RAMUS 21 SeGMeNTeD, POSTeRIOR RAMUS 22 SeGMeNTeD; cIRRUS V (15), (15); cIRRUS VI (15), (16). INTeRMeDIATe SeGMeNTS Of RAMI Of cIRRUS IV WITH 3 PAIRS Of SeRRULATe SeTAe (FIG. 29H); INTeRMeDIATe SeGMeNTS Of RAMI Of cIRRUS V WITH 5 PAIRS Of SeRRULATe SeTAe (FIG. 30C); INTeRMeDIATe SeGMeNTS Of RAMI Of cIRRUS VI WITH 4 PAIRS Of SeRRULATe SeTAe (FIG. 30E); DISTAL PAIR LONGeST, PROXIMAL PAIR SHORTeST (FIG. 30E). PeNIS LONG (1.6 TIMeS LeNGTH Of cIRRUS VI), ANNULATeD, WITH ScATTeReD SHORT, SIMPLe SeTAe (FIG. 30G). PeDIceL WITH SHARP BASIDORSAL POINT (FIG. 30H), APeX BeARING SHORT, SIMPLe SeTAe (FIG. 30I). HABITAT. ON THe cORALS Favites abdita, Favites flexuosa (DANA, 1846) AND Pavona venosa (TAIWAN MAIN ISLAND AND DONGSHA ATOLL). Distribution. RecORDeD IN JAPAN, TAIWAN MAIN ISLAND AND ADjAceNT OUTLyING ISLANDS (INcLUDING SIAO LIU-QIAO, KUeI SHAN ISLAND AND GReeN ISLAND) AND DONGSHA ATOLL. Etymology. Trevathana longidonta IS NAMeD fOR THe PReSeNce Of A LONG TOOTH ON THe INTeRNAL SURfAce Of THe TeRGUM. Remarks. THIS SPecIeS HAS A LONG, POINTeD TOOTH ON THe INTeRNAL SURfAce Of THe TeRGUM, WHIcH eXTeNDS BeyOND THe BASAL MARGIN Of THe TeRGUM. THIS feATURe IS ALSO PReSeNT IN Trevathana sarae BRIcKNeR, SIMON-BLecHeR & AcHITUV, 2010. HOWeVeR, Trevathana sarae DOeS NOT HAVe cONIcAL SPINeS ON cIRRUS III, AND THUS DIffeRS fROM T. longidonta sp. nov. Trevathana taiwanus sp. nov. HTTP://zOOBANK.ORG/URN: LSID:zOOBANK.ORG:AcT:6B52B28A-1952-4761-98C8-A8D2BE6623C5 FIGUReS 2I, J; 31–38 Trevathana sp. nov. 2. Chan et al., 2013: 328, figs. 290–298. Material examined. HOLOTyPe: ASIZCR000362, SHANfU FISHING HARBOR, SIAO-LIU-QIAO ISLAND, TAIWAN (22o20.20’N, 120o, 21.43’E), AUGUST 2010, cOLL. B.K.K. CHAN, ON cORAL Platygyra lamellina (EHReNBeRG, 1834). PARATyPeS: ASIZCR000363, SHANfU FISHING HARBOR, SIAO-LIU-QIAO ISLAND, TAIWAN (22o20.20’N, 120o, 21.43’E), AUGUST 2010, cOLL. B.K.K. CHAN, ON cORAL Platygyra lamellina. ASIZCR000364, DATA SAMe AS ASIZCR000363. Diagnosis. ScUTAL WIDTH 5 TIMeS LONGeR THAN HeIGHT. OccLUDeNT MARGIN cURVeD. MeDIAN cLOSeD fURROW cURVeD, ReAcHING 5/6 WIDTH Of ScUTUM. ARTIcULAR MARGIN WITH SeMIcIRcULAR, INTeRLOcKING TOOTH, WIDTH Of TOOTH ABOUT 3/4 HeIGHT Of ARTIcULAR MARGIN. ADDUcTOR PLATe PReSeNT, eXTeNDING fROM BASAL MARGIN. TeRGUM TRIANGULAR, BASAL MARGINS LONGeR THAN ScUTAL AND OccLUDeNT MARGINS, INTeRNAL TOOTH ABSeNT. SPUR WIDe, BLUNT, LONGITUDINAL MeDIAN fURROW TRIANGULAR, WIDTH INcReASING fROM ScUTAL MARGIN TO BASAL MARGIN. Description. SHeLL OVAL, cOVeReD By cORAL WHeN ALIVe (FIG. 2I, J). SHeLL fLAT (8.0 MM BD HOLOTyPe), eLLIPTIcAL, PLATeS fUSeD, eXTeRNAL SURfAce WITH 25 WHITe (AfTeR cLeANING AND PReSeRVATION) RADIATING ROWS WITH UP TO 7 PROjecTIONS IN A ROW (FIG. 31A). CIRcUMfeReNce Of BASe Of SHeLL WITH 31 SHORT PROjecTIONS, PROjecTIONS MARGIN SeRRATeD (FIG. 31B). ORIfIce eLLIPTIcAL, ABOUT 1/3 BASAL ROSTRO-cARINAL DIAMeTeR LOcATeD cLOSeR TO cARINAL MARGINS THAN ROSTRAL MARGINS. ScUTUM AND TeRGUM WHITe, SePARATeD (FIG. 31C–F). ScUTUM TRANSVeRSALLy eLONGATeD, TeRGAL MARGIN 5 TIMeS LONGeR THAN OccLUDeNT MARGIN (FIG. 31C–D). OccLUDeNT MARGIN cURVeD. MeDIAN cLOSeD fURROW cURVeD, fURROW LeNGTH ABOUT 5/6 LeNGTH Of ScUTUM, WITH 14 SIMILAR-SIzeD TeeTH ALONG MARGINS Of fURROW (FIG. 31C). ARTIcULAR MARGIN WITH A LARGe, SeMIcIRcULAR INTeRLOcKING TOOTH, WIDTH Of TOOTH ReAcHING 3/4 LeNGTH Of ARTIcULAR MARGIN, GROWTH LINeS ON TOOTH. EXTeRNAL SURfAce Of ScUTUM WITH ADDUcTOR PLATe eXTeNDING fROM BASAL MARGIN (FIG. 31C). TeRGUM TRIANGULAR, BASAL MARGINS LONGeR THAN ScUTAL AND OccLUDeNT MARGINS (FIG. 31E). INNeR SIDe Of ScUTAL MARGIN WITH SeMIcIRcULAR DePReSSION AccOMMODATING INTeRLOcKING TOOTH Of ScUTUM (FIG. 31F). SPUR WIDe, BLUNT, eXTeRNAL SURfAce WITH TRIANGULAR-SHAPeD, LONGITUDINAL, MeDIAL fURROW, WIDTH Of MeDIAL fURROW INcReASING fROM DIRecTION Of ScUTAL MARGIN TO BASAL MARGIN (FIG. 31E). MAXILLA SUBTRIANGULAR (FIG. 32A), SIMPLe SeTAe DISTALLy (FIG. 32B) AND ON INTeRIOR MARGIN (FIG. 32C). MAXILLULe cUTTING eDGe STRAIGHT, WITHOUT NOTcH, ROW Of 9–11 SPINeS (cOUNTS fROM 3 SPecIMeNS, (FIG. 32D, G, H), SeTAe cLOSe TO SUPeRIOR eDGe Of cUTTING MARGIN LARGeST; INfeRIOR MARGIN NeXT TO cUTTING eDGe WITH DeNSe, fINe, SIMPLe SeTAe (FIG. 32F), LOWeR eDGe Of cUTTING MARGIN WITH LONG, SIMPLe SeTAe (FIG. 32E). MANDIBLe WITH 4 OR 5 TeeTH, eXcLUDING INfeRIOR ANGLe (cOUNTS fROM 3 SPecIMeNS, FIG. 33A, E, H). SecOND TO fOURTH TeeTH BIDeNTATe (FIG. 33B, F), \ fIRST 3 TeeTH OccUPyING MORe THAN 2/3 LeNGTH Of cUTTING eDGe, LOWeR MARGIN SHORT (FIG. 33D, G, H), INfeRIOR ANGLe BLUNT (FIG. 33G). MANDIBULAR PALP OVAL, eLONGATeD (FIG. 34A), SIMPLe SeTAe ON DISTAL TIP (FIG. 34B), SeRRULATe SeTAe ON INTeRIOR MARGIN (FIG. 34C). LABRUM BILOBeD, LOBeS SePARATeD By V-SHAPeD NOTcH, SINGLe SHARP TOOTH ON eAcH LOBe (cONSISTeNT IN 2 SPecIMeNS, FIG. 34D–H). CIRRUS I WITH RAMI UNeqUAL, ANTeRIOR RAMUS LONG, SLeNDeR, 15 SeGMeNTeD (FIGS. 35A, 36A), POSTeRIOR RAMUS 6 SeGMeNTeD, BeARING SeRRULATe SeTAe (FIG. 36B–D). CIRRUS II WITH RAMI SLIGHTLy UNeqUAL, ANTeRIOR RAMUS 10 SeGMeNTeD, POSTeRIOR RAMUS 9 SeGMeNTeD (FIGS. 35B, 36E), BeARING SeRRULATe SeTAe (FIG. 36F–H). CIRRUS III WITH ANTeRIOR RAMUS SLIGHTLy LONGeR THAN POSTeRIOR RAMUS, 11 AND 9 SeGMeNTS ReSPecTIVeLy (FIGS. 35C, 37A), BeARING SeRRULATe SeTAe (FIG. 37A–D). DORSAL SIDe Of POSTeRIOR RAMUS WITH cOMBS, cONIcAL SPINeS ABSeNT (FIG. 37B). CIRRI IV–VI LONG, SLeNDeR, RAMI SIMILAR IN LeNGTH (FIGS. 35D–F, 37E, 38A–B). CIRRUS IV ANTeRIOR RAMUS 17 SeGMeNTeD, POSTeRIOR RAMUS 21 SeGMeNTeD; cIRRUS V (22), (22); cIRRUS VI (23), (16) SeGMeNTS. SeGMeNTS Of RAMI Of cIRRUS IV WITH 3 PAIRS Of SeRRULATe SeTAe (FIG. 37F–H); RAMI Of cIRRI V–VI WITH 4 PAIRS Of SeRRULATe SeTAe (FIG. 38C–F); DISTAL PAIR LONGeST, PROXIMAL PAIR SHORTeST, (FIGS. 35G–H, 38C, E). PeNIS LONG, 2 TIMeS LeNGTH Of cIRRUS VI, ANNULATeD, WITH ScATTeReD SHORT, SIMPLe SeTAe (FIG. 38G). PeDIceL WITH BLUNT BASIDORSAL POINT (FIG. 38G, H), APeX BeARING SHORT, SIMPLe SeTAe (FIG. 38I). Etymology. THIS SPecIeS IS NAMeD fOR ITS TyPe LOcALITy, TAIWAN. Habitat. AT PReSeNT ONLy RecORDeD ON THe cORAL Platygyra lamellina. Distribution. CURReNTLy ONLy RecORDeD fROM TAIWAN. Remarks. THeRe ARe ONLy fOUR Trevathana SPecIeS, T. noae, T. taiwanus sp. nov., T tureiae AND T. niuea, WHIcH DO NOT HAVe A TOOTH ON THe INTeRNAL SIDe Of THe TeRGUM. Trevathana taiwanus IS MORPHOLOGIcALLy SIMILAR TO T. noae AcHITUV & HOSIe, 2013 (See Key BeLOW). HOWeVeR, THe cONIcAL SPINeS ON THe DISTAL SeGMeNTS Of THe RAMI Of cIRRUS III THAT ARe fOUND IN T. noae ARe ABSeNT IN Trevathana taiwanus sp. nov.Published as part of Chan, Benny Kwok Kan, Chen, Yi-Yang, Achituv, Yair & Lin, Hsiu-Chin, 2017, Description of five new coral associated Barnacles of the genus Trevathana (Balanomorpha: Pyrgomatidae) in Pacific Waters, pp. 151-202 in Zootaxa 4363 (2) on pages 177-187, DOI: 10.11646/zootaxa.4363.2.1, http://zenodo.org/record/109875

    Cantellius hoegi Achituv, Tsang & Chan, 2009, sp. nov.

    No full text
    Cantellius hoegi sp. nov. (Figs 1–3) Materials examined. Holotype, ASIZCR 0 0 0 202, Dong-Qing-Wan, Lanyu Island, Taiwan (22 °01’, 121 ° 32 ’), 5–10 m, coll. B.K.K. Chan; paratype, ASIZCR 000203- 205, data same as holotype. Diagnosis. Wall with approximately 20 internal ribs; lengths of scutal basal and tergal margins subequal; tergum with broad spur, external spur furrow shallow, spur length approximately 1 / 2 length of scutal margin. Description. Parietes slightly projecting above coral surface, covered by coral skeleton overlying external ribs, number of ribs indistinct (Fig. 1 A, B). Rostro-carinal diameter to 4 mm; wall of 4 parietes, approximately 20 internal radial ribs radiating from central orifice, some secondary ribs reaching 1 / 2 way between wall circumference and orifice (Fig. 1 C); tubes between sheath and parietes largely filled. Orifice oval; 1 / 5 of rostro-carinal diameter. Sheath pigmented, orange, with concentric growth ridges extending more than 1 / 2 way down internal surface of parietes (Fig. 1 C). Carina wider than rostrum. Basis white, solid, thin, shallow cup-shape. Opercular valves thin, orange-red. Scutum triangular, basal margins slightly longer than tergal margins; externally growth ridges coarse, crossed by fine striae, alternate ridges forming teeth on occuludent margins (Fig 1 D, F). Tergal portion of scutum inflected. Apical angle approximately 60 °, 11–14 rows of round pits at apical angle forming honeycomb-like surface (Fig. 1 E). Basal margins sinusoidal. Internally adductor ridge not extending beyond basal margin. Pit of lateral depressor muscle small; rostral tooth absent. Tergum (Fig. 1 G, I) with blunt spur, spur width approximately 1 / 2 tergal width, external furrow shallow, open from apex to spur base, angle between spur and basal margin obtuse. Pits similar to those on Scutum, forming honeycomb-like surface at apex (Fig. 1 H). Sinusoidal, fine growth ridges on tergum surface. Tergal wing height approximately 1 / 2 tergal length (including spur). Internally small pits for tergal depressor muscle present (Fig. 1 I). Trophi: Mandibles with quadridentoid cutting edge (Fig. 2 A), 2 nd and 4 th teeth bidentate, first 3 teeth occupying more then 3 / 4 length of cutting edge (Fig. 2 C). Lower mandibular margin smooth, without fine setae or spines (Fig. 2 A). Lateral side of mandible bearing serrulate setae with fine setules (Fig. 2 B). Labrum with deep, V-shaped notch, 2 large teeth on each side of notch (Fig. 2 D). Maxillule straight, row of 9 strong spines of differing sizes (Fig. 4 E), serrulate setae at base of large spines (Fig. 2 F). Mandibular palp and maxilla bearing serrulate setae with short and dense setules (Fig. 2 G, H, I, J). Cirri: Cirrus I with rami unequal, exopodite of 13 articles, endopodite of 5 (Fig. 3 A). Setae on rami serrulate (Fig. 3 B) with dense setules. Protopodite bearing serrulate setae with sparsely distributed setules (Fig. 3 C). Cirrus II with expopodite and endopodite similar length, 6–7 articles (Fig. 3 D), rami bearing serrate setae with 3 rows of setules (Fig. 3 E, F), setules distally curved, sharply pointed (Fig. 3 F). Cirrus III with exopodite and endopodite thin (Fig. 3 G), rami bearing serrate setae with 3 rows of setules (Fig. 3 H). Protopod bearing plumose setae with long setules (Fig. 3 C, I). Cirri IV–VI similar (Fig. 3 J), articles of rami with 2–3 pairs of thin, serrulate setae, distal pair longest (Fig. 3 K). Etymology. The species is named in honor of Jens T. Høeg’s (University of Copenhagen, Denmark) in recognition of his contribution to the study of cirripede phylogeny.Published as part of Achituv, Yair, Tsang, Ling Ming & Chan, Benny Kwok Kan, 2009, A new species of Cantellius and a redescription of C. sextus (Hiro, 1938) (Cirripedia, Balanomorpha Pyrgomatidae) from the elephant skin coral, Pachyseris speciosa (Dana, 1846) (Scleractinia, Agariciidae) from Taiwan, pp. 15-28 in Zootaxa 2022 on pages 17-19, DOI: 10.5281/zenodo.18610

    Looking backwards to look forwards: the role of natural history in temperate reef ecology

    No full text
    Temperate reefs are superb tractable systems for testing hypotheses in ecology and evolutionary biology. Accordingly there is a rich history of research stretching back over 100 years, which has made major contributions to general ecological and evolutionary theory as well as providing better understanding of how littoral systems work by linking pattern with process. A brief resumé of the history of temperate reef ecology is provided to celebrate this rich heritage. As a community, temperate reef ecologists generally do well designed experiments and test well formulated hypotheses. Increasingly large datasets are being collected, collated and subjected to complex meta-analyses and used for modelling. These datasets do not happen spontaneously – the burgeoning subject of macroecology is possible only because of the efforts of dedicated natural historians whether it be observing birds, butterflies, or barnacles. High-quality natural history and old-fashioned field craft enable surveys or experiments to be stratified (i.e. replicates are replicates and not a random bit of rock) and lead to the generation of more insightful hypotheses. Modern molecular approaches have led to the discovery of cryptic species and provided phylogeographical insights, but natural history is still required to identify species in the field. We advocate a blend of modern approaches with old school skills and a fondness for temperate reefs in all their splendour

    Two new species of sand-bubbler crabs, Scopimera, from North China and the Philippines (Crustacea: Decapoda: Dotillidae)

    No full text
    Two undescribed species of Scopimera are herein described. Scopimera sheni sp. nov. from Qingdao, represents the fourth species of the genus to be recognized from North China. Scopimera philippinensis sp. nov. is the first record of the genus from the Philippines. Morphologically both new species belong to the "normal form" Scopimera (sensu Kemp 1919). Amongst other characters, each can be distinguished by its diagnostic male first gonopod. Mitochondrial cytochrome oxidase I (COI) gene sequences showed two distinct clades. An East Asia group (Chinese coasts, Japan, Korea and Taiwan) consisting of S. globosa De Haan, 1835, S. ryukyuensis Wong, Chan et Shih, 2010, S. sheni sp. nov., S. longidactyla Shen, 1932 and S. curtelsona (= S. cutelsoma) Shen, 1936; and a Southeast Asia group consisting of the closely related S. philippinensis sp. nov. and S. intermedia Balss, 1934. A dichotomous key is provided for all "normal forms" of Scopimera species

    Molecular phylogeny and origin of symbiotic coral and sponge associated barnacles (Thoracica: Cirripedia)

    No full text
    [[sponsorship]]生物多樣性研究中心[[note]]已出版;有審查制度;具代表

    Comparative phylogeography and cryptic diversity of intertidal barnacles in the NW Pacific

    No full text
    [[sponsorship]]生物多樣性研究中心[[note]]已出版;有審查制度;具代表

    A distributed learning model for Freshwater Ecology Practical Classes

    No full text
    This paper describes a case study where a distributed learning model was used to enhance the traditional teaching of a freshwater ecology practical class by providing students with a student-centred constructivist environment. Prior to the practical session, a website was created and students were encouraged to think about the morphological adaptations of stream organisms. They were then divided into groups and taken to a real stream to collect specimens and bring them back to the laboratory for further examination and discussion. After the practical, each student group was required to produce a web page concerning the adaptations of the stream organisms, to answer a set of online tutorial questions, and to participate in web-based discussion. Feedback by questionnaire showed that the great majority of students enjoyed working with the website and found the content very useful. More than half of the students preferred this type of web-assisted, student-centred practical to conventional practicals, while about a third showed no special preference between the two approaches
    corecore