New Zealand Journal of Botany
←
→
Page content transcription
If your browser does not render page correctly, please read the page content below
This article was downloaded by: [144.76.86.22] On: 07 August 2015, At: 15:54 Publisher: Taylor & Francis Informa Ltd Registered in England and Wales Registered Number: 1072954 Registered office: 5 Howick Place, London, SW1P 1WG New Zealand Journal of Botany Publication details, including instructions for authors and subscription information: http://www.tandfonline.com/loi/tnzb20 Fungi decaying stems of fallen tawa (Beilschmiedia tawa) trees in the central North Island of New Zealand a a I. A. Hood & J. F. Gardner a Scion (New Zealand Forest Research Institute Ltd) , PO Box 3020, Rotorua, 3046, New Zealand Published online: 18 Feb 2010. To cite this article: I. A. Hood & J. F. Gardner (2009) Fungi decaying stems of fallen tawa (Beilschmiedia tawa) trees in the central North Island of New Zealand, New Zealand Journal of Botany, 47:2, 115-119, DOI: 10.1080/00288250909509797 To link to this article: http://dx.doi.org/10.1080/00288250909509797 PLEASE SCROLL DOWN FOR ARTICLE Taylor & Francis makes every effort to ensure the accuracy of all the information (the “Content”) contained in the publications on our platform. However, Taylor & Francis, our agents, and our licensors make no representations or warranties whatsoever as to the accuracy, completeness, or suitability for any purpose of the Content. Any opinions and views expressed in this publication are the opinions and views of the authors, and are not the views of or endorsed by Taylor & Francis. The accuracy of the Content should not be relied upon and should be independently verified with primary sources of information. Taylor and Francis shall not be liable for any losses, actions, claims, proceedings, demands, costs, expenses, damages, and other liabilities whatsoever or howsoever caused arising directly or indirectly in connection with, in relation to or arising out of the use of the Content. This article may be used for research, teaching, and private study purposes. Any substantial or systematic reproduction, redistribution, reselling, loan, sub-licensing, systematic supply, or distribution in any form to anyone is expressly forbidden. Terms & Conditions of access and use can be found at http://www.tandfonline.com/page/terms- and-conditions
New Zealand Journal of Botany, 2009, Vol. 47: 115-119 115 0028-825X/09/4702-0115 © The Royal Society of New Zealand 2009 Short communication Fungi decaying stems of fallen tawa (Beilschmiedia tawa) trees in the central North Island of New Zealand I. A. HOOD INTRODUCTION J. F. GARDNER As part of a programme to determine the decompo- Scion (New Zealand Forest Research Institute Ltd) sition rates of coarse woody debris in indigenous PO Box 3020 forests (Beets et al. 2008), we have investigated the Rotorua 3046, New Zealand principal basidiomycete decay fungi active within fallen trees at two locations in the central North Island (Hood et al. 1989, 2004, 2008). Tree species studied Downloaded by [144.76.86.22] at 15:54 07 August 2015 Abstract The principal decay fungi active within were Dacrydium cupressinum Lamb., Nothofagus the decomposing stems of six uprooted trees of fusca (Hook.f.) Oerst, N. menziesii (Hook.f.) Oerst, Beilschmiedia tawa in a dense podocarp forest were and Prumnopitys taxifolia (D.Don) de Laub. A determined by isolating onto a culture medium significant finding was that major decomposers of selective for basidiomycetes. The most common all four species included Ganoderma applanatum fungi obtained were species of Armillaria and sensu Wakef. and species of Armillaria (Fr.) Staude. Ganoderma applanatum sensu Wakef., a finding Subsequent to this work we have undertaken a sim ilar consistent with comparable results from other examination of the predominant decay fungi active indigenous tree species in earlier central North Island in uprooted trees of another important tree species, studies. The ascomycete species Kretzschmaria Beilschmiedia tawa (A.Cunn.) Kirk (Lauraceae), and zelandica, present in two of the trees, was obtained the results of the study form the basis of this report. only after eliminating benomyl and streptomycin as Data obtained were included along with those from constituents from the selective culture medium. A the other species in the decay rate analyses of Beets previously determined spatial relationship between et al. (2008). This note reports additional information fruiting by G. cf. applanatum and presence within not included in that publication. the stem, as revealed by isolation, was supported in this study. It therefore appears that for B. tawa, also, distribution of fruitbodies is a reliable indicator of internal colonisation by this species. MATERIALS AND METHODS The investigation was undertaken in a dense podocarp Keywords Beilschmiedia tawa; Armillaria; forest in Whirinaki Forest Park near Minginui east Ganoderma cf. applanatum; Kretzschmaria of Murupara, in the sam e stand as that described for zelandica; podocarp forest; coarse woody debris; the trees of D. cupressinum and P. taxifolia (Hood et wood decay; decomposition; isolation; basidiocarp; al. 2004). Six uprooted £. tawa trees were arbitrarily ascocarp selected within a distance of 250 m, five having fallen during a storm in 1982, and the sixth between 1982 and 1997. Stem diameters at breast height (1.4 m above original ground level) averaged 44.0 ± 10.8 cm (mean and standard deviation). In April 2007, three discs 4-6 cm thick were cut from each tree, one at breast height, a second at approximately one-half, and a third at approximately three-quarters along the available stem length. Distances between discs averaged 5.8 ± 2.5 m (mean and standard B08033; Online publication date 26 June 2009 deviation; range, 2.8-9.9 m), and diameters of Received 25 September 2008; accepted 3 April 2009 the 18 discs averaged 37.8 ± 12.4 cm (mean and
116 New Zealand Journal of Botany, 2009, Vol. 47 12 6-12 0-E Fig. 1 Design for isolating from each disc (diagrammatic). After Isolation points * cutting two mutually opposite sec- tors along the horizontal diameter, each was split aseptically down the radial longitudinal plane. Isola- tions were then made from the new surface at points along a radius in the zones 0-6.0, 6.1-12.0, and >12.0 cm deep. Sector a Disc Sector b Downloaded by [144.76.86.22] at 15:54 07 August 2015 standard deviation). Discs were sealed individually for numbers on each type of culture medium) or in polythene bags and stored at 4°C. Where present, separately for those on each medium in each depth a record was made of the distribution of fruitbodies zone. The probability of a relationship between of the decay fungus G. cf. applanatum along the fruiting by G. cf. applanatum and presence of this stems in relation to the disc sampling positions. species within stems was examined using Fisher's Locations of fruitbodies and signs of other species exact test. Data from all trees were used to construct were also noted. a 2 x 2 contingency table of discs yielding or not Isolations for decay fungi were undertaken in the yielding cultures of this species by those with or laboratory within 7 weeks of field sampling. Two without fruitbodies. Discs were accepted as positive radially oriented blocks (sectors) were cut extending if they were cut at a locus within a sequence of in from the circumference towards the centre of fruitbodies, and negative if they were situated outside each disc. Sectors were selected on opposite sides and not closer than 4 m to the nearest fruitbody. of the disc along the horizontal diameter, as in the intact stem (Fig. 1). Each block was split aseptically down the radial longitudinal plane and, as described in Hood et al. (2008), 20 small chips were cut from RESULTS AND DISCUSSION the freshly exposed surface along a radial line, Basidiomy cete fungi were cultured from an average six from the outer 0-6.0 cm zone, seven from the of 59% of isolation attempts on both media in all 6.1-12.0 cm zone, and seven from the zone deeper radial depth zones (Table 1). Therefore, by 25 years than 12.0 cm. Chips were plated onto a medium after windfall, decay fungi had penetrated throughout selective for basidiomycetes consisting of 2% malt the stems of the Beilschmiedia tawa study trees. agar supplemented with 100 ppm streptomycin The species identified were comparatively low in sulfate and 10 ppm benomyl. For two trees bearing number (Table 1), no doubt reflecting the relatively fruitbodies of a xylariaceous ascomycete, a second limited sampling coverage (three discs from each set of chips from both sectors in all discs was plated tree). However, this pattern is typical of results from onto 2% malt agar without the potentially inhibiting the earlier studies in this forest, and the sampling ingredients present in the selective medium. In all, was sufficient to identify the major decay fungi 918 isolation attempts were made from the six trees. present in these stems. A full inventory of the Emerging cultures were sorted and identified where complete decomposer biodiversity would require possible as previously described (Hood et al. 2008). more intensive sampling supplemented by periodic Percentages of isolation attempts yielding different collection offruitbodies of uncommon species likely fungi were calculated for "units" consisting of each to be missed altogether during isolation (Hood et al. of the three radial depth zones in each sector. Total 2008). The most frequently obtained basidiomycetes number of units was 103 (6 trees x 3 discs x 2 sectors were species of GanodermaandArmillaria. Isolates of y- 3 depth zones, less 5 units where the sectors did Armillariawere not determined further, but previous not extend deeper than 12 cm radially). Values were records from this site were of A. novae-zelandiae averaged across all units (weighting proportionately (G.Stev.)Herink and A limonea (G.Stev.)Boesew.,
Hood & Gardner—Fungi decaying tawa stems 117 both of which are known onB. tawa (MacKenzie & wereRigidoporusconcrescens(Mont)Rajchenb. and Shaw 1977; Hood et al. 2004). Ganoderma isolates Sistotrema sp., both of which have also previously were accepted as G. cf. applanatum because of the been cultured from different tree species at this plentiful fruiting by this species, only, on the study site (Table 1). Cultures of Sistotrema sp., formerly trees (Hood et al. 2004). The prominence of these identified as S. brinkmannii (Bres.) J.Erikss. (Hood fungi among all the isolates obtained is consistent et al. 2004), were not distinguishable from those with results from the other indigenous tree species of S. otagense (G.Cunn.) Stalpers & P.K.Buchanan in which the same species were also predominant, isolated from material at the Nothofagus location. along with Cyclomyces tabacinus (Mont.) Pat. in Cultures of S. otagense were identified by features Nothofagus hosts (Hood et al. 2004, 2008). that included basidiospore size and morphology Armillaria sp(p). were especially common among (Hood et al. 2008). Since basidiospores were not seen the basidiomycetes present withinS. tawa, andwere during the present or earlier studies at the Whirinaki cultured from 28 (78%) of the 36 possible sectors site, the precise identity of the Sistotrema species at at a mean yield of 41% of isolation attempts from this location has not been confirmed. A number of all units (Table 1). In contrast to the earlier studies other basidiomycete species isolated less frequently with other tree species, in which isolates were in the Nothofagus study were not obtained from B. obtained more towards the periphery, Armillaria tawa (Hood et al. 2008). Downloaded by [144.76.86.22] at 15:54 07 August 2015 sp(p). showed extensive colonisation throughout all Fruitbodies of the ascomycete Kretzschmaria depth zones inS. tawa. Of the 64 units from which zelandica J.D.Rogers & Y.M.Ju were present Armillaria sp(p). were obtained, 56 (91%) yielded on two study trees 75 m apart associated with a cultures of these species alone, implying exclusive white rot accompanied by black, pseudosclerotial occupation. Stumps of B. tawa were once a cause for zone plates (Table 1; collections NZFRI 5406M, concern as a focus for armillaria root disease centres 5407M, 5429M, 5430M, Forest Research Mycology when indigenous forests were formerly replaced by Herbarium, Rotorua, New Zealand). This species plantations of Firms radiata D.Don (MacKenzie was isolated deeper than 6 cm from one or both & Shaw 1977; Shaw & Calderon 1977; van der sectors, respectively, from a single disc from each tree Pas 1981). Ganoderma cf. applanatum was also (cultures NZFS 2920, 2921, 2922, Forest Research prominent among the basidiomycetes in B. tawa, Culture Collection, Rotorua, New Zealand). Cultures being cultured from six sectors in three discs from were obtained only on the malt agar medium devoid two trees, with an average yield of 15% of isolation of benomyl and streptomycin, indicating that, for a attempts across all units. Sole occupancy was also comprehensive evaluation of coarse woody debris reasonably high for this species, which was obtained that includes ascomycete species, isolation should exclusively from 60% of the units in which it was be undertaken using both culture media. However, present. Other basidiomycetes identified in this study although locally significant, yields of K. zelandica Table 1 Means of percentage isolation attempts1 yielding decay fungi, by radial depth zone and isolation medium. Malt agar with benomyl and Malt agar only streptomycin sulfate (six trees) (two trees) Radial depth zone (cm) Radial depth zone (cm) Fungi No. trees^ 0-6.0 6.1-12 >12 0-6.0 6.1-12 >12 Ganoderma cf. applanatum 2 7 11 16 22 23 32 Armillaria sp(p.). 6 43 45 39 28 52 34 Rigidoporus concrescens 1 0 2 2 0 0 0 Sistotrema sp. 3 2 0 0 1 0 0 Other basidiomycetes 4 2 2 0 0 0 1 Kretzschmaria zelandica 2 0 0 0 0 1 18 All basidiomycetes 6 54". 59 57 52 75 67 All decay fungi •6 54 59 57 52 77 85 n (No. sectors) 36 36 31 12 11 12 'Rounded to nearest integer. 2 Number of trees yielding specified fungi (data from both isolation media).
118 New Zealand Journal of Botany, 2009, Vol. 47 averaged only 7% across all units on the malt agar (based on comparisons between context isolates medium, suggesting that not too much is lost at the from authenticated fruitbodies: NZFRI 5476M, wider scale when resource constraints necessitate 5477M; NZFS 3005-3013; I. A. Hoodunpubl. data). isolation using the basidiomycete selective medium Fruitbodies of G. australe were not found on the alone. Cultures of K. zelandica stained positive fallen stems of any of the tree species sampled during with moderate intensity in oc-naphthol, confirming our different investigations even though one was the production of laccase, and indicating white rot collected from a dead standing tree at the Nofhofagus activity by this species (Stalpers 1978). site (NZFRI 5505M). Ganoderma australe has a For a number of species of decay fungi, a spatial broad distribution range but m ay occur infrequently, association was indicated between fruiting or other requiring the sampling of greater numbers of fallen fungal signs and occurrence within tree stems. trees before it is detected. Airborne basidiospores of Fructifications of K. zelandica were present at the G. cf. applanatum (as G. mastoporum (Lev.) Pat.) same disc positions on both trees from which it were abundant during an aerobiological investigation was isolated, and were observed only at these loci. in Auckland, whereas those of G. australe were Characteristic honeycomb pocket decay spanned the collected only occasionally (Hasnain et al. 1984). two disc positions from which R. concrescens was Many more herbarium specimens have been collected obtained (Hood et al. 1989), and new fruitbodies of G. cf. applanatum than of G. australe (Buchanan Downloaded by [144.76.86.22] at 15:54 07 August 2015 of this species were present on a cut face at one of &Wilkie 1995). these positions on a subsequent visit. Evidence of typical older decay in the form of surface scalloping was also apparent on a number of the study trees along the lengths of stem from which Armillaria ACKNOWLEDGMENTS was isolated. Cultures of G. cf. applanatum were also obtained only from stem segments bearing Thanks are expressed for assistance during this study fruitbodies, and for this species a significant to Peter Beets, Brenda Callan, Graeme Oliver, Stephen Pearce, and Greg Steward, and to two anonymous referees relationship was demonstrated between fruiting and who made useful comments on the manuscript. Funding internal colonisation (p = 0.0049, n = 18, Fisher's was provided by the Foundation for Research, Science and exact test). This result supports the earlier conclusion Technology, and access to the site was facilitated through that visible fruiting by G. cf. applanatum is a reliable the Department of Conservation. indicator of occurrence within stems as determined by isolation of cultures. In this smaller study, reliability was 100%, since all discs with or without associated fruitbodies yielded or did not yield cultures of G. cf. REFERENCES applanatum, except for one disc that yielded no Beets PN, Hood IA, Kimberley MO, Oliver GR, Pearce cultures despite the presence of fruitbodies (which SH, Gardner JF 2008. Coarse woody debris nevertheless verified its presence). With B. tawa decay rates for seven indigenous tree species in this conclusion must be tempered by the lighter the central North Island of New Zealand. Forest sampling and the possibility that parts of the stem Ecology and Management 256: 548-557. not examined by isolation might have been colonised Buchanan PK, Wilkie JP 1995. Taxonomy of New by G. cf. applanatum without showing fruitbodies. Zealand Ganoderma—two non-laccate species. However, this does not apply to the earlier studies In: Buchanan PK, Hseu RS, Moncalvo JM ed. in which sampling was more frequent, and it is Ganoderma: systematics, phytopathology and reasonable to assume that behaviour inB. tawa does pharmacology. Proceedings of Contributed Sym- not differ. After more than two decades, colony size posium 59A,B, Fifth International Mycological will be firmly delineated, with no advancing mycelial Congress, Vancouver, Canada, 14-21 August 1994. Taipei, National Taiwan University. Pp. front potentially preceding fruitbody production. 7-17. Fallen trees colonised by G. cf. applanatum Hasnain SM, Newhook FJ, Wilson JD, Corbin JB 1984. decompose more rapidly than those occupied by First report of Ganoderma allergenicity in New other decay fungi (Beets et al. 2008). However, Zealand. New Zealand Journal of Science 27: whether a secondNew Zealand species, Ganoderma 261-267. australe (Fr.) Pat., behaves similarly remains to Hood IA, Sandberg CJ, Kimberley MO 1989. A decay be confirmed, notwithstanding that both species study of windthrown indigenous trees. New are morphologically indistinguishable in culture Zealand Journal of Botany 27: 281-297.
Hood & Gardner—Fungi decaying tawa stems 119 Hood IA, Beets PN, Kimberley MO, Gardner JF, Oliver GR, Pearce S 2004. Colonisation of podocarp coarse woody debris by decomposer basidiomycete fungi in an indigenous forest in the central North Island of New Zealand. Forest Ecology and Management 196: 311-325. Hood IA, Beets PN, Gardner JF, Kimberley MO, Power MWP, Ramsfield TD 2008. Basidiomycete decay fungi within stems of Nothofagus windfalls in a Southern Hemisphere beech forest. Canadian Journal of Forest Research 38: 1897-1910. MacKenzie M, Shaw III CG 1977. Spatial relationships between Armillaria root-rot of Pinus radiata seedlings and the stumps of indigenous trees. New Zealand Journal of Forestry Science 7: 374-383. Shaw CG III, Calderon S 1977. Impact of Armillaria root rot in plantations of Pinus radiata established Downloaded by [144.76.86.22] at 15:54 07 August 2015 on sites converted from indigenous forest. New Zealand Journal of Forestry Science 7: 359-373. Stalpers JA 1978. Identification of wood-inhabiting Aphyllophorales in pure culture. Centraalbureau voor Schimmelculrures. Studies in Mycology 16: 1-248. van der Pas JB 1981. A statistical appraisal of Armillaria root rot in New Zealand plantations of Pinus radiata. New Zealand Journal of Forestry Science 11: 23-36.
You can also read