12.07.2015 Views

A new species and re-disposed taxa in Repetophragma - CBS

A new species and re-disposed taxa in Repetophragma - CBS

A new species and re-disposed taxa in Repetophragma - CBS

SHOW MORE
SHOW LESS

Create successful ePaper yourself

Turn your PDF publications into a flip-book with our unique Google optimized e-Paper software.

Mycosphe<strong>re</strong>A <strong>new</strong> <strong>species</strong> <strong>and</strong> <strong>re</strong>-<strong>disposed</strong> <strong>taxa</strong> <strong>in</strong> <strong>Repetophragma</strong>Castañeda-Ruiz RF 1 , He<strong>re</strong>dia G 2 , Arias RM 2 , McKenzie EHC 3 , Hyde KD 4 , Stadler M 5* ,Saikawa M 6 , Gené J 7 , Guarro J 7 , Iturriaga T 8 , M<strong>in</strong>ter DW 9 <strong>and</strong> Crous PW 101 Instituto de Investigaciones Fundamentales en Agricultura Tropical “Alej<strong>and</strong>ro de Humboldt”, Calle 1 Esq. 2, Santiagode Las Vegas, C. Habana, Cuba, C.P. 172002 Instituto de Ecología, A.C., Cong<strong>re</strong>gación El Haya, Xalapa, Veracruz 91070, Mexico3 L<strong>and</strong>ca<strong>re</strong> Research, Private Bag 92170, Auckl<strong>and</strong>, New Zeal<strong>and</strong>4 School of Science, Mac Fah Luang University, Thasud, Chiang Rai 57100, Thail<strong>and</strong>5 University of Bay<strong>re</strong>uth, Dept. Mycology, Universitätstr. 30, D-95544 Bay<strong>re</strong>uth, Germany6 Tokyo Gakugei University, Dept. Biology, Nukuikita-machi, Koganei-shi, Tokyo 184-8501, Japan7 Unitat de Microbiologia, Facultat de Medic<strong>in</strong>a i Ciencies de la Salut, Universitat Rovira i Virgili, 43201 Reus,Tarragona, Spa<strong>in</strong>8 Departamento Biología de Organismos, Universidad Simón Bolívar, Apartado 89000. Sartenejas, Baruta, Edo Mir<strong>and</strong>a,Venezuela9 CABI, Bakeham Lane, Egham, Sur<strong>re</strong>y, TW20 9TY, United K<strong>in</strong>gdom10 <strong>CBS</strong>-KNAW Fungal Biodiversity Cent<strong>re</strong>, Uppsalalaan 8, 3584 CT Ut<strong>re</strong>cht, The Netherl<strong>and</strong>sCastañeda-Ruiz RF, He<strong>re</strong>dia G, Arias RM, McKenzie EHC, Hyde KD, Stadler M, Saikawa M,Gené J, Guarro J, Iturriaga T, M<strong>in</strong>ter DW, Crous PW. 2011 – A <strong>new</strong> <strong>species</strong> <strong>and</strong> <strong>re</strong>-<strong>disposed</strong> <strong>taxa</strong> <strong>in</strong><strong>Repetophragma</strong>. Mycosphe<strong>re</strong> 2(3), 273–289.A <strong>new</strong> <strong>species</strong> of <strong>Repetophragma</strong>, collected on plant material from “Aguita Fria” Veracruz, Mexico,<strong>and</strong> from Canaima National Park, Bolivar State, Venezuela is described <strong>and</strong> illustrated.<strong>Repetophragma</strong> paracamb<strong>re</strong>nse sp. nov. is characterized by subobclavate to somewhat lageniform,truncate at the base, 8−10-septate, brown, mostly verruculose, sometimes smooth conidia. Twelve<strong>new</strong> comb<strong>in</strong>ations a<strong>re</strong> proposed for <strong>taxa</strong> p<strong>re</strong>viously <strong>in</strong>cluded <strong>in</strong> Sporidesmium <strong>and</strong> Endophragmiella.A comparative table <strong>and</strong> key to <strong>Repetophragma</strong> <strong>species</strong> a<strong>re</strong> provided.Key words – anamorphic fungi – cloud fo<strong>re</strong>st – Guiana fo<strong>re</strong>st – systematicsArticle InformationReceived 17 Febuary 2011Accepted 10 May 2011Published onl<strong>in</strong>e 9 August 2011*Cor<strong>re</strong>spond<strong>in</strong>g author: Marc Stadler – e-mail – marc.stadler@t-onl<strong>in</strong>e.deIntroductionSubramanian (1992) e<strong>re</strong>cted the genus<strong>Repetophragma</strong> dur<strong>in</strong>g a <strong>re</strong>vision of SporidesmiumL<strong>in</strong>k, <strong>and</strong> <strong>in</strong>cluded n<strong>in</strong>e <strong>species</strong>. <strong>Repetophragma</strong>biseptata (M.B. Ellis) Subram. wasdesignated as the type <strong>species</strong>. The diagnosticcharacters of the genus a<strong>re</strong> macronematousconidiopho<strong>re</strong>s with several annellations producedafter a few or numerous enteroblasticpercur<strong>re</strong>nt proliferations of the conidiogenouscell, <strong>and</strong> euseptate conidia with a conicotruncatebasal cell, which seccede schizolytically.The comb<strong>in</strong>ation of these featu<strong>re</strong>sseparates the genus <strong>Repetophragma</strong> fromSporidesmiella P.M. Kirk, which has distoseptateconidia (McKenzie 1995). Subsequently,ten other <strong>species</strong> have been added to thegenus: <strong>Repetophragma</strong> camb<strong>re</strong>nse (M.B. Ellis)McKenzie (McKenzie 1995), R. cubense(Mercado) J. Mena (Mena et al. 2000), R. goidanichii(Rambelli) W.P. Wu (Wu & Zhuang2005), R. <strong>in</strong>flatum (Berk. & Ravenel) W.P. Wu(Wu & Zhuang 2005), R. ontariense (Matsush.)W.P. Wu (Wu & Zhuang 2005), R. s<strong>in</strong>enseW.P. Wu (Wu & Zhuang 2005), R. fasciatum(R.F. Castañeda) R.F. Castañeda, Gusmão &273


Saikawa (Castañeda et al. 2006), R. filiferum(R.F. Castañeda) R.F. Castañeda et al.(Castañeda et al. 2006), R. calongei J. Mena,Silvera & Gené (Silvera-Simón et al. 2009, <strong>and</strong>R. gondwanamycetis Mar<strong>in</strong>c., M.J. W<strong>in</strong>gf. &Crous (Mar<strong>in</strong>cowitz et al. 2008).Dur<strong>in</strong>g an expedition <strong>in</strong> February 2010through the protected a<strong>re</strong>as of Veracruz State,Mexico, a conspicuous fungus from the genus<strong>Repetophragma</strong> was collected on decay<strong>in</strong>gwood. A specimen collected <strong>in</strong> a tropical fo<strong>re</strong>st<strong>in</strong> southern Venezuela dur<strong>in</strong>g 2005 proved tobe the same fungus. These specimens showeddiffe<strong>re</strong>nces from p<strong>re</strong>viously described <strong>taxa</strong> <strong>and</strong>a<strong>re</strong> he<strong>re</strong><strong>in</strong> described <strong>and</strong> illustrated as a <strong>new</strong><strong>species</strong> of <strong>Repetophragma</strong>.Materials <strong>and</strong> methodsDur<strong>in</strong>g February 2010 around 80 samplesof microfungi we<strong>re</strong> collected <strong>in</strong> “Aguita Fria”,Veracruz, Mexico (Fig. 21). Individual collectionswe<strong>re</strong> placed <strong>in</strong> paper bags, taken to thelaboratory, <strong>and</strong> <strong>in</strong>cubated at 25°C <strong>in</strong> Petridishes placed <strong>in</strong> a moist chamber composed ofplastic conta<strong>in</strong>ers (50 L capacity) with 200 mLof sterile water plus 2 mL of glycerol, <strong>and</strong>exam<strong>in</strong>ed at <strong>re</strong>gular <strong>in</strong>tervals for the p<strong>re</strong>senceof microfungi. Aeration was supplied by open<strong>in</strong>gthe conta<strong>in</strong>ers for 5 to 10 m<strong>in</strong>utes at 45m<strong>in</strong>utes <strong>in</strong>tervals dur<strong>in</strong>g a week. Mounts we<strong>re</strong>p<strong>re</strong>pa<strong>re</strong>d <strong>in</strong> polyv<strong>in</strong>yl alcohol-glycerol (8.0 g <strong>in</strong>100 mL of water, plus 5 mL of glycerol) <strong>and</strong>measu<strong>re</strong>ments made at a magnification of×1000. The same methodology was followedfor specimens collected dur<strong>in</strong>g an expedition <strong>in</strong>April 2005 to Luepa, Gran Sabana a<strong>re</strong>a,Canaima National Park, as part of a series ofexpeditions to collect wood decompos<strong>in</strong>g fungi<strong>in</strong> a tropical fo<strong>re</strong>st <strong>in</strong> southern Venezuela.Micrographs we<strong>re</strong> obta<strong>in</strong>ed with a ZeissAxioskop 40 microscope <strong>and</strong> a Leitz Dialux 20EB microscope. Holotype material is deposited<strong>in</strong> the Herbarium of the “Instituto de EcologíaA.C., Xalapa (XAL) <strong>and</strong> a paratype at HerbarioNacional de Venezuela <strong>in</strong> Caracas (VEN).Taxonomy<strong>Repetophragma</strong> paracamb<strong>re</strong>nse R.F. Castañeda, He<strong>re</strong>dia & McKenzie, sp. nov.Figs 1−20MycoBank 519657Etymology − G<strong>re</strong>ek, para- similar to, bythe side of; camb<strong>re</strong>nse, epithet of similar<strong>species</strong> <strong>in</strong> the genus <strong>Repetophragma</strong>.Figs 1−19 − <strong>Repetophragma</strong> paracamb<strong>re</strong>nse,photomicrographs from holotype (XALCB1700). 1−12 Conidia. 13−19 Conidiogenouscells <strong>and</strong> conidia. Scale bars = 10 µm.Coloniae <strong>in</strong> substrato naturali effusae,pilosae, nigrae vel atrobrunneae. Myceliumpartim superficiale et partim <strong>in</strong> substrato immersum,ex hyphis septatis, ramosis, brunneis,verruculosis vel laevibus. Conidiophora macronematosa,mononematosa, e<strong>re</strong>cta, <strong>re</strong>cta velleviter geniculata, 5−8-septata, sursum perproliferata,ad usque 10 proliferationes successivas,180−350 × 7−10 µm, atrobrunnea adbasim, pallidiora ad apicem. Cellulae conidiogenaemonoblasticae, term<strong>in</strong>ales, <strong>in</strong> conidiophoris<strong>in</strong>corporatae, <strong>in</strong>determ<strong>in</strong>atae, cum proliferationesenteroblasticis percur<strong>re</strong>ntis de<strong>in</strong>de274


Mycosphe<strong>re</strong>Fig. 20 − <strong>Repetophragma</strong> paracamb<strong>re</strong>nse, draw<strong>in</strong>gs from holotype (XAL CB1700). Conidiopho<strong>re</strong>s,conidiogenous cells <strong>and</strong> conidia. Scale bar = 10 µm.aliquot cyathiformibus et annuliformibus visae.Conidiorum secessio schizolytica. Conidiasolitaria, subobclavata vel aliquot lageniformia,truncata ad basim, leviter constricta ad cellulasubapicale et rotundata ad apicem, 8−10-septata,utrimque laevia et subhyal<strong>in</strong>a, verruculosaet brunnea cetero, sed atrobunnea vel nigra adsepta, sicca, 35−55 × 10−13 µm. Teleomorphosisignota.Colonies on the natural substratum effuse,hairy, black or dark brown. Myceliumsuperficial <strong>and</strong> immersed, composed of septate,branched, brown, verruculose or smooth hyphae.Conidiopho<strong>re</strong>s macronematous, mononematous,simple, e<strong>re</strong>ct, straight or slightly geniculatetowards the apex, 5−8-septate, annellateabove, with up to 10 annellations, 180−350 ×7−10 µm, dark brown at the base <strong>and</strong> palebrown towards the apex. Conidiogenous cellsmonoblastic, term<strong>in</strong>al, <strong>in</strong>tegrated, <strong>in</strong>determ<strong>in</strong>ate,annellidic with numerous cyathiformenteroblastic percur<strong>re</strong>nt proliferations. Conidialsecession schizolytic. Conidia solitary, subobclavateto somewhat lageniform, truncate at thebase, slightly constricted at the subapical cell<strong>and</strong> rounded at the apex, 8−10-septate, septablack, subhyal<strong>in</strong>e <strong>and</strong> smooth at the ends, othercells verruculose <strong>and</strong> brown, 35−55 × 10−13µm, dry. Teleomorph unknown.Habitat − on decay<strong>in</strong>g twig of unidentifiedplant, on fallen decompos<strong>in</strong>g decorticatedbranch.Known distribution − Mexico, Venezuela.Material exam<strong>in</strong>ed: Mexico, Veracruz, “Aguita275


Mycosphe<strong>re</strong><strong>Repetophragma</strong> quadrilocula<strong>re</strong> (Matsush.)R.F. Castañeda, McKenzie & K.D. Hyde,comb. nov. Fig. 52MycoBank 519668Basionym − Endophragmiella quadrilocula<strong>re</strong>Matsush, Matsushima MycologicalMemoirs 7: 51, 1993.<strong>Repetophragma</strong> term<strong>in</strong>aliae (Deighton) R.F.Castañeda, McKenzie & K.D. Hyde, comb.nov. Fig. 56MycoBank 519669Basionym − Sporidesmium term<strong>in</strong>aliaeDeighton, <strong>in</strong> Deighton & Cejp, MycologicalPapers 117: 25, 1969.The ability to generate one or numerouselongations of the conidiogenous cells can beused to separate <strong>taxa</strong> at the generic level, butcannot be used to diffe<strong>re</strong>ntiate <strong>species</strong>, s<strong>in</strong>cethe number of proliferations (annellations) canbe <strong>in</strong>fluenced by environmental conditions.Wang (1990) po<strong>in</strong>ted out that “the annellationson an annellopho<strong>re</strong> a<strong>re</strong> the <strong>re</strong>sults of the<strong>re</strong>generation of enti<strong>re</strong> <strong>new</strong> conidiogenous cells,orig<strong>in</strong>at<strong>in</strong>g either from the penultimate cells orfrom endohyphae”, it can be confirmed withthe pale or colorless pigmentation of apicalproliferation that characterized <strong>new</strong> materialformed dur<strong>in</strong>g the conidiogenous events <strong>and</strong><strong>re</strong>generation of the conidiogenous cells.To assist <strong>in</strong> identification of <strong>species</strong> asynoptic table with the pr<strong>in</strong>cipal diagnosticfeatu<strong>re</strong>s is provided (Table 1), along with a keyto the <strong>species</strong>.Table 1 Comparison of described <strong>and</strong> <strong>re</strong>-<strong>disposed</strong> <strong>Repetophragma</strong> <strong>species</strong>.Species Conidiopho<strong>re</strong>s Conidia Refe<strong>re</strong>ncesMorphology <strong>and</strong> size (µm) Morphology <strong>and</strong> size (µm)R. aburiense Brown, up to 14annellations, 7−80 × 4−6R. afrormosiae Pale brown or olivaceousbrown, up to 5 annellations,8−30 × 4−6R. apice<strong>in</strong>flatum Pale brown, subhyal<strong>in</strong>etowards apex, 1−7annellations, 20−45(−110) ×3 −4R. biseptatum Mid to dark brown, 0−18-annellations, 55−190 ×4.5−6R. calongei Brown to dark brown, 4−9annellations, 32−75 × 5−7R. camb<strong>re</strong>nse Reddish brown or darkbrown, paler towards apex,up to 6 annellations, 60−300× 7−11R. cubense Dark brown, 3−17annellations, 50−180 × 6−9Obclavate, rostrate, 2−4-septate, brown, palertowards apex, smooth orverruculose, 40−65 × 6−7Obclavate, often rostrate <strong>and</strong>curved, 7−12-septate,sometimes 1−2 obliquesepta, brown, paler towardsapex, smooth, 60−100 ×8−10Cyl<strong>in</strong>drical, globose toslightly <strong>in</strong>flated at apex,4−12-septate, pale brownwith hyal<strong>in</strong>e basal cell,smooth, 27−80(−110) ×4−5.5Navicular, 2-septate, brownto dark brown, basal cellsubhyal<strong>in</strong>e, smooth, 17−23 ×7−8Subcyl<strong>in</strong>drical tosubfusiform, 12−27-septate,brown to mid brown,smooth, 80−165 × 8−10.5Subfusiform, 7−10-septate,brown with paler end cells,smooth, (47−)53−63(−70) ×10−14Obclavate, ra<strong>re</strong>ly fusiform,rostrate, 6−13-septate, darkgolden brown, pale at base<strong>and</strong> towards apex, obscu<strong>re</strong>b<strong>and</strong> at septa, smooth,50−200 × 13−18, rostrum upto 130 longEllis (1958, 1976),Subramanian (1992)Ellis (1963, 1976),Subramanian (1992)Matsushima (1995)Ellis (1963, 1976),Subramanian (1992)Silvera-Simón et al.(2009)Ellis (1958),McKenzie (1995)Mercado (1984a, b),Mena-Portales et al.(2000)277


Table 1 (Cont<strong>in</strong>ued) Comparison of described <strong>and</strong> <strong>re</strong>-<strong>disposed</strong> <strong>Repetophragma</strong> <strong>species</strong>.Species Conidiopho<strong>re</strong>s Conidia Refe<strong>re</strong>ncesMorphology <strong>and</strong> size (µm) Morphology <strong>and</strong> size (µm)R. dennisii Brown, pale brown towardsapex, 7−27 annellations,80−310 × 6−8Ellipsoid to oval, (2−)3−4-septate, brown, apical cellpale brown, smooth, 23−32Kirk (1983), Subramanian(1992), Castañeda-Ruiz etal. (2003), Wu & ZhuangR. ellisii Yellow-brown near base,pale straw towards apex,3−8 annellations, 60−180 ×3.5−5.0R. fasciatum Dark brown, pale browntowards apex, 4−8annellations, 100−150 × 5−9R. filiattenuatum (*) Dirty brown, pale at apex,up to 7 annellations, 30−150× 6−10R. filiferum Brown, 4−10 annellations,60−100 × 4−6R. filisporum (**) Dirty brown, pale towardsapex, up to 4 annellations,20−50(−100) × 3.5−5R. fragmentisporum (**) Dirty brown, pale near apex,3−6 annellations <strong>and</strong>sometimes with somesympodial elongations, up to40 × 3−4R. goidanichii Brown to dark brown, 5−11annellations, 40−78 × 5−8R. gondwanamycetis Brown, pale near apex, 0−1annellations, 70−160 × 5−6R. <strong>in</strong>dicum Dark brown, 7−12annellations, 50−100 × 5−8× 11−13Obclavate, acicular rostrate,4−5-septate, yellow-brown,two middle cells darkerstraw-colou<strong>re</strong>d, apical cellhyal<strong>in</strong>e, basal cellsubhyal<strong>in</strong>e, smooth, 40−90 ×7−9, rostrum up to 60 longEllipsoid to oval, with afiliform, straight apicalappendage, 5-septate,brown, dark brown at middlecells, black b<strong>and</strong> at septa,smooth, 22−27 × 10−12,appendage 80−90 longObclavate, cyl<strong>in</strong>dricalrostrateabove, 7−23-septate,brown, subhyal<strong>in</strong>e towardsapex, smooth, 80−520 ×10−16, rostrum up to 400long. On natural substratum68−165 × 12−14Broad fusiform to navicular,with a filiform, straight orflexuous apical appendage,6−8-septate, mid palebrown, smooth, 28−40 ×8−10, appendage up to 100longNarrow obclavate tosubcyl<strong>in</strong>drical, 6−40-septate,dirty brown, pale brown orsubhyal<strong>in</strong>e towards apex,smooth, 50−300 × 4−5. Onnatural substrate 27−70 ×4−5.5Cyl<strong>in</strong>drical, 6−20-septate,pale olivaceous, smooth,36−85 × 4−5Cyl<strong>in</strong>drical, 7−9-septate,brown, smooth, 40−52 ×5−7Cyl<strong>in</strong>drical or fusiform,slightly curved or straight,3−12-septate, pale to darkbrown, subhyal<strong>in</strong>e end cells,smooth, (25−)31–34(−45) ×5−9Obclavate, slightlyconstricted at septum, 1-septate, pale golden brown,smooth, 30−42 × 7−9(2005)Pirozynski (1972), Ellis(1976)Castañeda-Ruiz (1985),Gr<strong>and</strong>i & Silva (2003),Castañeda-Ruiz et al.(2006)Matsushima (1983),Subramanian (1992),Wu & Zhuang (2005)Pirozynski (1972), Ellis(1976), Castañeda-Ruiz etal. (2006)Matsushima (1993)Matsushima (1993)Hughes (1979), Wu &Zhuang (2005)Mar<strong>in</strong>cowitz et al. (2008)Ellis (1976), Subramanian(1992)278


Table 1 (Cont<strong>in</strong>ued) Comparison of described <strong>and</strong> <strong>re</strong>-<strong>disposed</strong> <strong>Repetophragma</strong> <strong>species</strong>.Mycosphe<strong>re</strong>SpeciesConidiopho<strong>re</strong>sMorphology <strong>and</strong> size (µm)R. <strong>in</strong>flatum Brown, 4−8 annellations,80−400 × 6−9R. laxisporum Brown, up to 10annellations, 25−85 ×3.5−7.0R. longiphorum Dark brown, brown towardsapex, up to 14 annellations,350−800 × 7−10R. moniliforme Brown, dark brown nearbase, 1−4 annellations, 9−50× 4−5R. omahutaense (***) Brown, with 3−10-annellations, up to 70 long<strong>and</strong> 3−4 wideR. ontariense Pale brown to brown, with6−14-annellations, 30−50 ×5−7R. paracamb<strong>re</strong>nse Dark brown at the base <strong>and</strong>pale brown towards theapex, with up to 10-annellations, 180−350 ×7−10R. perproliferatum Brown, pale brown towardsthe apex, with 1−3-annellations, up to 70 long<strong>and</strong> 3−4 wideR. peruamazonicum (***) Brown, with 1−4-annellations, 25−65 × 4−6R. quadrilocula<strong>re</strong> (***) Brown, pale brown towardsapex, 2−5-annellations, up to70 × 3−4ConidiaMorphology <strong>and</strong> size (µm)Obclavate, sigmoid, 3−5-septate, dark <strong>re</strong>ddish-brownor dark brown second <strong>and</strong>occasionally third cells, palebrown or subhyal<strong>in</strong>e othercells, smooth, 45−90 ×11−18Fusiform to obclavate,subulate at apex, 6−7-septate, brown, end cellssubhyal<strong>in</strong>e, smooth, 25−39 ×7−9Obclavate, rostrate, 3−6-septate, f<strong>re</strong>quently 4-septate,median cells transverselystriate <strong>and</strong> brown, end cellssmooth <strong>and</strong> pale brown,45−85 × 9−10Moniliform, 8−22-septate,brown <strong>and</strong> verrucose at base<strong>and</strong> middle body, palebrown <strong>and</strong> smooth towardsapex, 55−280 × 6−10Cyl<strong>in</strong>drical, 2−5-septate,pale brown, smooth, 8−28 ×4−5Fusiform or obclavate,8−11-septate, pale brown tomid brown, smooth,100−140 ×15−20Sub-obclavate to somewhatlageniform, truncate at thebase, slightly constricted atthe subapical cell <strong>and</strong>rounded at the apex, 8−10-septate, subhyal<strong>in</strong>e <strong>and</strong>smooth at the ends, othercells verruculose <strong>and</strong> brown,with black septa, 35−55 ×10−13Obclavate, with a narrow,tape<strong>re</strong>d apical appendage,2−3-septate, second cellbrown, the other cells paler,smooth, 18−35 × 3, apicalcell 6−21 longObclavate to slightlycyl<strong>in</strong>drical, 5−8-septate,brown <strong>and</strong> pale brown at theend cells, smooth, 23−32 ×6−8Obovate to subglobose, 3-septate, dark brown middle<strong>and</strong> basal cells, pale brownat apex, smooth, 16−21 ×8−13.On natural substrate 20−24× 11−14Refe<strong>re</strong>ncesEllis (1958, 1971),Matsushima (1975), Wu &Zhuang (2005)Castañeda-Ruiz (1985)Castañeda-Ruiz &Kendrick (1991)Matsushima (1993)Matsushima (1985)Wu & Zhuang (2005)P<strong>re</strong>sent paper.Castañeda-Ruiz &Kendrick (1991)Matsushima (1993)Matsushima (1993)279


Table 1 (Cont<strong>in</strong>ued) Comparison of described <strong>and</strong> <strong>re</strong>-<strong>disposed</strong> <strong>Repetophragma</strong> <strong>species</strong>.SpeciesConidiopho<strong>re</strong>sMorphology <strong>and</strong> size (µm)ConidiaMorphology <strong>and</strong> size (µm)R. s<strong>in</strong>ense Pale brown to brown, 4−5- Obclavate, rostrate, slightlyannellations, 40−150 × 4−6 curved, 6−9-septate, palebrown to mid brown, smooth,35−45 × 7−9R. subulatum Olivaceous brown, up to 7 Obclavate to subfusiform,annellations, 20−90 × 8−10 7−10-septate, dark olivaceousbrown, pale brown towardsapex, smooth, 90−160 ×15−19R. term<strong>in</strong>aliae Pale olivaceous, up to 8 Cyl<strong>in</strong>drical, curved, 4−5-annellations, 20−80 × 4−5.5 septate, pale olivaceous,smooth, 50−75 × 6.5−8R. wroblewskii Pale to mid golden brown, Obclavate or subfusiform,up to 8 annellations, 7−40 × 3−4-septate, pale to mid5−8golden brown, smooth orverruculose, 30−46 × 9−11R. zambiense Pale olivaceous, slightly Subcyl<strong>in</strong>drical, often curved,s<strong>in</strong>uous, 2−5 annellations, slightly wider at middle cells,11−50 × 4−6.54−13-septate, occasionallywith a longitud<strong>in</strong>al septum <strong>in</strong>one or two central cells, paleolivaceous to deep olivaceous,smooth, 39−104 × 7−11(*) On V8 agar media (**) On banana leaf piece (***) On CMA mediaRefe<strong>re</strong>ncesWu & Zhuang (2005)Ellis (1958, 1976),Subramanian (1992)Deighton (1969), Ellis(1976)Ellis (1958, 1976),Subramanian (1992)Deighton (1969), Ellis(1976), Subramanian(1992)Key to <strong>Repetophragma</strong> <strong>species</strong>1 Conidia 1-septate, obclavate, slightlyconstricted at the septum, pale goldenbrown, smooth, 30−42 × 7−92 µm ...........................................R. <strong>in</strong>dicum (Fig. 42)Conidia with mo<strong>re</strong> than 1 septum..........22(1) Conidia with an apical rostrum (rostrate)...............................................................3Conidia without an apical rostrum (notrostrate or taper<strong>in</strong>g to the apex).............83(1) Conidia usually with fewer than 6 septa.................................................................4Conidia usually with mo<strong>re</strong> than 5 septa.54(3) Conidia obclavate, with a narrow, tape<strong>re</strong>dapical appendage, 2−3-septate, secondcell brown, other cells paler, smooth,18−35 × 3 µm, apical cell 6−21 µm long....................R. perproliferatum (Fig. 50)Conidia obclavate, 2−4-septate, brown,paler towards apex, smooth orverruculose, 40−65 × 6−7 µm ...............................................R. aburiense (Fig. 22)Conidia obclavate, acicular, 4−5-septate,yellow-brown, with two middle cellsdarker straw-colou<strong>re</strong>d, apical cell hyal<strong>in</strong>e,basal cell subhyal<strong>in</strong>e, smooth, 40−90 ×7−9 µm, rostrum up to 60 µm long ......R.ellisii (Fig. 34)Conidia obclavate or subfusiform, 3−4-septate, pale to mid golden brown,smooth or verruculose, 30−46 × 9−11µm.......................... R. wroblewskii (Fig. 57)Conidia ellipsoid to oval, with a filiform,straight apical appendage, 5-septate,brown <strong>and</strong> dark brown at the middle cells,with a black b<strong>and</strong> at the septa, smooth,22−27 × 10−12 µm, appendage 80−90µm long................. R. fasciatum (Fig. 35)5(3) Conidia usually with fewer than 10 septa............................................................... 6Conidia sometimes with mo<strong>re</strong> than 10septa....................................................... 76(5) Conidia obclavate, 3−6-septate, f<strong>re</strong>quently4-septate, median cells transverselystriate <strong>and</strong> brown, end cells smooth <strong>and</strong>pale brown, 45−85 × 9−10 µm ..........................................R. longiphorum(Fig. 46)280


Mycosphe<strong>re</strong>Conidia broad fusiform to navicular, witha filiform, straight or flexuous apicalappendage, 6−8-septate, mid pale brown,smooth, 28−40 × 8−10 µm, appendage upto 100 µm long........R. filiferum (Fig. 37)Conidia obclavate, slightly curved, 6−9-septate, pale brown to mid brown,smooth, 35−45 × 7−9 µm ..........................................................R. s<strong>in</strong>ense (Fig. 53)Conidia fusiform to obclavate, subulateat the apex, 6−7-septate, brown, withsubhyal<strong>in</strong>e end cells, smooth, 25−39 ×7−9 µm................R. laxisporum (Fig. 45)7(5) Conidia obclavate, curved, 7−12-septate,sometimes 1−2 oblique septa, brown,paler towards the apex, smooth, 60−100× 8−10 µm ........ R. afrormosiae (Fig. 23)Conidia obclavate, ra<strong>re</strong>ly fusiform, 6−13-septate, dark golden brown, pale at thebase <strong>and</strong> towards the apex, with obscu<strong>re</strong>b<strong>and</strong> at the septa, smooth, 50−200 ×13−18 µm, rostrum up to 130 µm long ....................................R. cubense (Fig. 29)Conidia obclavate, cyl<strong>in</strong>drical-rostrateabove, 7−23-septate, brown <strong>and</strong> subhyal<strong>in</strong>etowards the apex, smooth, 80−520 ×10−16 µm, rostrum up to 400 µm long .......................... R. filiattenuatum (Fig. 36)8(2) Conidia mostly cyl<strong>in</strong>drical or subcyl<strong>in</strong>drical,not curved ...................................9Conidia mostly cyl<strong>in</strong>drical or subcyl<strong>in</strong>drical,curved .......................................10Conidia mostly obclavate, not curved ornot sigmoid, 6−40-septate, dirty-brown,pale brown or subhyal<strong>in</strong>e towards theapex, smooth, 50−300 × 4−5 µm.......................................... R. filisporum (Fig. 38)9(8) Conidia 4−5-septate, pale olivaceous,smooth, 50−75 × 6.5−8.0 µm .......................................... R. omahutaense (Fig. 48)Conidia 7−9-septate, brown, smooth,40−52 × 5−7 µm ................................................................. R. goidanichii (Fig. 40)Conidia globose to slightly <strong>in</strong>flated at theapex, 4−12-septate, pale brown withhyal<strong>in</strong>e basal cell, smooth, 27−80(−110)× 4.0−5.5 µm ..R. apice<strong>in</strong>flatum (Fig. 24)Conidia 6−20-septate, pale olivaceous,smooth, 36−85 × 4−5 µm .......................................... R. fragmentisporum (Fig. 39)Conidia 12−27-septate, brown to midbrown, smooth, 80−165 × 8−10.5 µm.....................................R. calongei (Fig. 26)10(8) Conidia 4−5-septate, pale olivaceous,smooth, 50−75 × 6.5−8.0 µm ............................................. R. term<strong>in</strong>aliae (Fig. 56)Conidia slightly wider above the middlecells, 4−13-septate, occasionally with alongitud<strong>in</strong>al septum <strong>in</strong> one or two centralcells, pale olivaceous to deep olivaceous,smooth, 39−104 × 7−11µm ..................................................R. zambiense (Fig. 58)Conidia 3−12-septate, pale to dark brown,with subhyal<strong>in</strong>e end cells, smooth,(25−)31−34(−45) × 5−9 µm .....................................R. gondwanamycetis (Fig. 41)11(8) Conidia 5−8-septate, brown <strong>and</strong> palebrown at the end cells, smooth, 23−32 ×6−8 µm ..... R. peruamazonicum (Fig. 51)Conidia 3−5-septate, dark <strong>re</strong>ddish-brownor dark brown second <strong>and</strong> occasionallythird cells, other cells pale brown orsubhyal<strong>in</strong>e, smooth, 45−90 × 11−18 µmR.<strong>in</strong>flatum...................................... (Fig. 43)Conidia 7−10-septate, dark olivaceousbrown <strong>and</strong> pale brown towards the apex,smooth, 90−160 × 15−19 µm .........................................R. subulatum (Fig. 54, 55)12(8) Conidia 8−11-septate, pale brown to midbrown, smooth, 100−140 × 15−20 µm.................................R. ontariense (Fig. 49)Conidia 7−10-septate, brown with pale<strong>re</strong>nd cells, smooth, (47−)53−63 (−70) ×10−14 µm .....R. camb<strong>re</strong>nse (Figs 27−28)Conidia slightly constricted at the subapicalcell <strong>and</strong> rounded at the apex, 8−10-septate, subhyal<strong>in</strong>e <strong>and</strong> smooth end cells,verruculose, <strong>and</strong> brown <strong>in</strong> the other cells,with black septa, 35−55 × 10−13 µm...................... R. paracamb<strong>re</strong>nse (Figs 1−20)13(8) Conidia navicular 2-septate, with subhyal<strong>in</strong>ebasal cell, other cells brown to darkbrown, smooth, 17−23 × 7−8 µm............281


Fig. 21 − Dr. V<strong>in</strong>icio Sosa dur<strong>in</strong>g a foray <strong>in</strong> “Aguita Fria” cloud fo<strong>re</strong>st, Veracruz, Mexico, tak<strong>in</strong>gsome pictu<strong>re</strong>s from the samples.............................R. biseptatum (Fig. 25)Conidia not navicular ..........................1414(13)Conidia ellipsoid to oval, (2−)3−4-septate, brown, apical cell pale brown,smooth, 23−32 × 11−13 µm .............................................. R. dennisii (Figs 30−33)Conidia obovate to subglobose, 3-septate,with dark brown middle <strong>and</strong> basal cells,<strong>and</strong> pale brown at the apex, smooth,16−21 × 8−13 µm ..........................................................R. quadrilocula<strong>re</strong> (Fig. 52)Conidia moniliform, 8−22-septate, brown<strong>and</strong> verrucose at the base <strong>and</strong> middle part,<strong>and</strong> pale brown <strong>and</strong> smooth towards theapex, 55−280 × 6−10 µm .................................................. R. moniliforme (Fig. 47)AcknowledgementsThe authors a<strong>re</strong> grateful to Dr Lori Carris(Wash<strong>in</strong>gton State University) for p<strong>re</strong>submission<strong>re</strong>view of this paper. Gabriela He<strong>re</strong>dia,R.M. Arias <strong>and</strong> R.F. Castañeda Ruiz a<strong>re</strong>thankful to CONABIO (Mexico) for f<strong>in</strong>ancialsupport through project IE004. T. Iturriaga isgrateful to FONACYT, Venezuela, for f<strong>in</strong>ancialsupport for project S1-2001000663. Theauthors thank Dr. Uwe Braun, Dr. Lori Carris,Dr. De-Wei Li, Dr. Felipe Wartchow, Dr.Antonio Hernández-Gutiér<strong>re</strong>z, Dr. Melissa282


Mycosphe<strong>re</strong>Figs 22−25 − <strong>Repetophragma</strong> spp. conidia.Redrawn from the orig<strong>in</strong>al descriptions. 22 R.aburiense. 23 R. afrormosiae. 24 R. apice<strong>in</strong>flatum.25. R. biseptatum. Scale bars = 10 µm.Figs 30−32 − <strong>Repetophragma</strong> dennisii, conidiopho<strong>re</strong>s,conidiogenous cells <strong>and</strong> conidia,photomicrographs from (USB C99/199). Scalebars 30, 31 = 10 µm, 32 = 20 µm.Figs 26−29 − <strong>Repetophragma</strong> spp. conidia.Redrawn from the orig<strong>in</strong>al descriptions. 26 R.calongei. 27−28 R. camb<strong>re</strong>nse. 29 R. cubense.Scale bar 27, 28 = 10 µm. 26, 29 = 20 µm.Figs 33−36 − <strong>Repetophragma</strong> spp. conidia.Redrawn from the orig<strong>in</strong>al descriptions. 33 R.dennisii. 34 R. ellisii. 35 R. fasciatum. 36 R.filiattenuatum. Scale bar 33, 34, 35 = 10 µm,36 = 40 µm.283


Figs 37−40 − <strong>Repetophragma</strong> spp. conidia. Redrawn from the orig<strong>in</strong>al descriptions. 37 R. filiferum,38 R. filisporum, 39 R. fragmentisporum, 40 R. goidanichii. Scale bar 37, 39, 40 = 10 µm, 38 = 20µm.Figs 41−44 − <strong>Repetophragma</strong> spp., conidia. 41 R. gondwanamycetis conidia. Adapted <strong>and</strong> <strong>re</strong>drawnfrom the orig<strong>in</strong>al descriptions. 42 R. <strong>in</strong>dicum. 43 R. <strong>in</strong>flatum, 44 R. laxisporum. Scale bars = 10 µm.284


Mycosphe<strong>re</strong>Fig. 45 − <strong>Repetophragma</strong> laxisporum, photomicrographsfrom holotype (INIFAT C85/13).Conidiopho<strong>re</strong>s, conidiogenous cells <strong>and</strong> conidia.Scale bars = 10 µm.Fig. 46 − <strong>Repetophragma</strong> longiphorum, draw<strong>in</strong>gof conidia from holotype (INIFAT C85/13). Scale bar = 10 µm.Figs 47−49 − <strong>Repetophragma</strong> spp., conidia. Redrawn from the orig<strong>in</strong>al descriptions. 47 R. moniliforme.48 R. omahutaense. 49 R. ontariense. Scale bar 47, 49 = 40 µm, 48 = 10 µm.285


Fig. 50 − <strong>Repetophragma</strong> perproliferatum, draw<strong>in</strong>g of conidia from holotype (INIFAT C91/10−4).Scale bar = 10 µm.Figs 51−54 − <strong>Repetophragma</strong> spp., conidia. Redrawn from the orig<strong>in</strong>al descriptions. 51 R.peruamazonicum. 52 R. quadrilocula<strong>re</strong>. 53 R. s<strong>in</strong>ense. Scale bar = 10 µm. 54 R. subulatum. Scalebar 51, 52, 53 = 10 µm, 54 = 40 µm.286


Mycosphe<strong>re</strong>Fig. 55 − <strong>Repetophragma</strong> subulatum. Conidiopho<strong>re</strong>s, conidiogenous cells <strong>and</strong> conidia, photomicrographsfrom (INIFAT C95/46). Scale bar = 10 µm.Figs 56 −58 − <strong>Repetophragma</strong> spp., conidia. Redrawn from the orig<strong>in</strong>al descriptions. 56 R. term<strong>in</strong>aliae.57 R. wroblewskii. 58 R. zambiense. Scale bars = 20 µm.Mardones, Dr. Cony Decock, Dr. Shaun Pennycook, Dr. Walter Gams, Dr. Rol<strong>and</strong> Kirschner,Dr. Sanjay K. S<strong>in</strong>gh, Dr. Antonio Hernández-Gutiér<strong>re</strong>z, Dr. Xiu Guo Zhang, Dr. DJ Bhat, Dr.Sanjay K. S<strong>in</strong>gh <strong>and</strong> Dr. G<strong>re</strong>gorio Delgado fortheir generous <strong>and</strong> valued assistance withliteratu<strong>re</strong> not otherwise available. We thankBeatriz Ramos, Mirtha Caraballo, Aliana Sosafor technical assistance. We also acknowledgethe facility provided by Dr. P.M. Kirk throughthe IndexFungorum website.287


Refe<strong>re</strong>ncesCastañeda-Ruiz RF. 1985 − Deuteromycot<strong>in</strong>ade Cuba. Hyphomycetes III. Instituto deInvestigaciones Fundamentales AgriculturaTropical, “Alej<strong>and</strong>ro de Humboldt”,Cuba 72.Castañeda-Ruiz RF, Kendrick B. 1991 −N<strong>in</strong>ety-n<strong>in</strong>e conidial fungi from Cuba<strong>and</strong> th<strong>re</strong>e from Canada. University ofWaterloo Biology Series 35, 1−132.Castañeda-Ruiz RF, Iturriaga T, M<strong>in</strong>ter DW,Saikawa M, Vidal G, Velázquez-Noa S.2003 − Microfungi from Venezuela. A<strong>new</strong> <strong>species</strong> of Brachydesmiella, a <strong>new</strong>comb<strong>in</strong>ation, <strong>and</strong> <strong>new</strong> <strong>re</strong>cords. Mycotaxon85, 211−229.Castañeda-Ruiz RF, Gusmão LFP, He<strong>re</strong>dia-Abarca G, Saikawa M. 2006 − Somehyphomycetes from Brazil. Two <strong>new</strong><strong>species</strong> of Brachydesmiella, two <strong>new</strong>comb<strong>in</strong>ations for <strong>Repetophragma</strong>, <strong>and</strong><strong>new</strong> <strong>re</strong>cords. Mycotaxon 95, 261−270.Deighton FC. 1969 − New genera <strong>and</strong> <strong>species</strong><strong>and</strong> <strong>re</strong>dispositions of some hyphomycetes,ma<strong>in</strong>ly African. Mycological, pp.117, 8−31.Ellis MB. 1958 − Clasterosporium <strong>and</strong> someallied dematiaceae phragmosporae hyphomycetes.I. Mycological Papers 70,1−89.Ellis MB. 1963 − Dematiaceous hyphomycetes.V. Mycological Papers 93, 1−33.Ellis MB. 1971 − Dematiaceous Hyphomycetes.Commonwealth Mycological Institute,Kew.Ellis MB. 1976 − Mo<strong>re</strong> Dematiaceous Hyphomycetes.Commonwealth MycologicalInstitute, Kew.Gr<strong>and</strong>i RAP, Silva TV. 2003 − Hyphomycetessob<strong>re</strong> folhas em descomposição deCaesalp<strong>in</strong>ia ech<strong>in</strong>ata Lam.: ocorrênciasnovas para o Brasil. Revista Brasileira deBotanica 26, 489−493.Hughes SJ. 1979 − Relocation of <strong>species</strong> ofEndophragmia auct. with notes on <strong>re</strong>levantgeneric names. New Zeal<strong>and</strong> JournalBotany 17, 139−188.Kirk PM. 1983 − New or <strong>in</strong>te<strong>re</strong>st<strong>in</strong>g microfungiIX. Dematiaceous hyphomycetesfrom Esher Common. Transactions of theBritish Mycological Society 80, 449−467.Mar<strong>in</strong>cowitz S, Crous PW, Groe<strong>new</strong>ald JZ,W<strong>in</strong>gfield MJ. 2008 − Microfungi occurr<strong>in</strong>gon Proteaceae <strong>in</strong> the fynbos. <strong>CBS</strong>Biodiversity Series 7, 1−166.Matsushima T. 1975 − Icones microfungorum aMatsushima lectorum. Published by T.Matsushima, Kobe.Matsushima T. 1983 − Matsushima MycologicalMemoirs No. 3. Matsushima FungusCollection, Kobe.Matsushima T. 1985 − Matsushima MycologicalMemoirs No. 4. Matsushima FungusCollection, Kobe.Matsushima T. 1993 − Matsushima MycologicalMemoirs No. 7. Matsushima FungusCollection, Kobe.Matsushima T. 1995 − Matsushima MycologicalMemoirs No. 8. Matsushima FungusCollection, Kobe.McKenzie EHC. 1995 − Dematiaceous hyphomyceteson P<strong>and</strong>anaceae. 5. Sporidesmiumsensu lato. Mycotaxon 56, 9−29.Mena-Portales J, Delgado-Rodríguez G, He<strong>re</strong>dia-Abarca G. 2000 − Nuevas comb<strong>in</strong>acionespara e<strong>species</strong> de SporidesmiumS.L. (Hongos mitospóricos). Boletín de laSociedad de Micologia de Madrid 25,265−269.Mercado SA. 1984a − Nuevas e<strong>species</strong> deDeightoniella, Phaeoisaria, Sporidesmiumy Taeniolella (Hyphomycetes) deCuba. Acta Botánica Cubana 21, 10.Mercado SA. 1984b. − Hifomicetes Demaciáceosde Sierra del Rosario, Cuba. EditorialAcademia, La Habana.Pirozynski KA. 1972 − Microfungi of TanzaniaI. Miscellaneous fungi on oil palm II.New hyphomycetes. Mycological Papers129, 1−64.Silvera-Simón C, Mena-Portales J, Gené J,Cano J, Guarro J. 2009 − <strong>Repetophragma</strong>calongei sp. nov. <strong>and</strong> other <strong>in</strong>te<strong>re</strong>st<strong>in</strong>gdematiaceous hyphomycetes from theNorth of Spa<strong>in</strong>. Anales del Jardín Botánicode Madrid 66S1, 33−39.Subramanian CV. 1992 − A <strong>re</strong>assessment ofSporidesmium (hyphomycetes) <strong>and</strong> some<strong>re</strong>lated <strong>taxa</strong>. Proceed<strong>in</strong>gs of the Indian288


Mycosphe<strong>re</strong>National Science Academy Botany 58,179−190.Wang CJK. 1990 − Ultrastructu<strong>re</strong> of percur<strong>re</strong>ntlyproliferat<strong>in</strong>g conidiogenous cells<strong>and</strong> classification. Studies <strong>in</strong> Mycology32, 49−64.Wu WP, Zhuang W. 2005 − Sporidesmium,Endophragmiella <strong>and</strong> <strong>re</strong>lated generafrom Ch<strong>in</strong>a. Fungal Diversity ResearchSeries 15, 1−351.289

Hooray! Your file is uploaded and ready to be published.

Saved successfully!

Ooh no, something went wrong!