Inoculum 63(3) - Mycological Society of America
Inoculum 63(3) - Mycological Society of America
Inoculum 63(3) - Mycological Society of America
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and amenity areas. The population dynamics and dispersal pathway <strong>of</strong> this<br />
pathogen in the US have not been well studied. In attempt to elucidate this, we<br />
isolated eight promising microsatellite markers from an enriched genomic library<br />
<strong>of</strong> Wcc. Seven <strong>of</strong> these markers were used to study the population diversity <strong>of</strong><br />
eastern and western US populations <strong>of</strong> Wcc and the association with phenotypic<br />
characteristics. In general, the microsatellite markers were highly polymorphic,<br />
with an observed heterozygosity <strong>of</strong> > 0.5. The eastern population was differentiated<br />
from the western population but both populations showed the presence <strong>of</strong> immigrant<br />
individuals across boundaries. Analysis <strong>of</strong> population structure with geography<br />
revealed a significant clinal expansion, r 2 = 0.11, P = 0.01, <strong>of</strong> Wcc within<br />
a radius <strong>of</strong> about 150 km. However, it became more stochastic with increase in<br />
distance. No host specific clusters were observed based on UPGMA clustering,<br />
suggesting a lack <strong>of</strong> association between host and pathogen genotypes.<br />
Norvell, Lorelei L 1 and Scott A Redhead 2 . 1 Mycotaxon, PNW Mycology<br />
Service, Portland OR 97229-1309 USA, 2 National <strong>Mycological</strong> Herbarium, Eastern<br />
Cereal & Oilseed Research Centre C.E.F., Agriculture & Agri-Food Canada,<br />
Ottawa, ON K1A 0C6 Canada. A mycologist’s guide to the Melbourne Code.<br />
The International Code <strong>of</strong> Nomenclature for algae, fungi, and plants<br />
(ICN) replaced the International Code <strong>of</strong> Botanical Nomenclature (ICBN) during<br />
the 2011 International Botanical Congress (IBC) in Melbourne. The new ICN permits<br />
diagnoses/descriptions in English (no longer requiring Latin) and electronic<br />
publication <strong>of</strong> fungal names (via PDFs in ISSN/ISBN numbered publications).<br />
With registration <strong>of</strong> fungal names required for valid publication in 2013, the IBC<br />
Nomenclature Committee for Fungi (NCF) is now moving to approve one or<br />
more nomenclatural registries. The ICN also excludes names <strong>of</strong> microsporidians<br />
and organisms treated in other Codes, refines typification procedures and spelling<br />
<strong>of</strong> sanctioned names, and recommends how to designate type cultures. The Melbourne<br />
Congress also referred mechanical typification issues and governance <strong>of</strong><br />
fungal nomenclature to special committees and approved NCF recommendations<br />
on the conservation and rejection <strong>of</strong> notable fungal names. The new ICN does not<br />
permit multiple names for fungi with pleomorphic life cycles, which the ICBN<br />
(under Art. 59) previously allowed for non-lichenized ascomycetes and basidiomycetes.<br />
After 2013, alternative new names will be either illegitimate or not<br />
valid, although alternatives published through 2012 may be valid or legitimate.<br />
Although teleomorph- and anamorph-typified names will compete equally for priority,<br />
the ICN dictates delay in adopting anamorph-typified names with priority<br />
over commonly used teleomorph-typified names. To buffer the effects <strong>of</strong> this<br />
major change regarding alternative names, NCF-sanctioned subcommittees will<br />
compile and adjudicate lists <strong>of</strong> conserved/rejected names <strong>of</strong> non-lichenized fungi<br />
(not restricted to the Ascomycota and Basidiomycota) for approval by the IBC.<br />
The NCF and International Commission on the Taxonomy <strong>of</strong> Fungi (ICTF) - collaborating<br />
to issue joint guidelines, updates, and advice - recognize that mycological<br />
opinion over the Art. 59 change is still deeply divided and must be considered.<br />
Nuhn, Mitchell, Roy E Halling, Manfred Binder, David S Hibbett, and Todd W<br />
Osmundson. Department <strong>of</strong> Biology, Clark University, 950 Main St, Worcester,<br />
MA 01610. The Boletineae <strong>of</strong> Queensland, Australia<br />
The Boletineae is a group <strong>of</strong> mushrooms with many species highly sought<br />
after by both animals and humans as food. The majority <strong>of</strong> Boletineae species are<br />
ectomycorrhizal with woody plants, making them important members <strong>of</strong> forest<br />
ecosystems. This study will provide the first biodiversity inventory <strong>of</strong> the Boletineae<br />
in Queensland, Australia, including three <strong>of</strong> Australia’s Biodiversity<br />
Hotspots and World Heritage listed sites. To accomplish the inventory, modern<br />
molecular and phylogenetic techniques will be used, in combination with traditional<br />
taxonomic methods. A sequence dataset <strong>of</strong> nuclear ribosomal large subunit<br />
(nuclsu) and translation elongation factor 1-alpha (tef1) sequences has been generated<br />
for the systematic overview <strong>of</strong> the Boletineae <strong>of</strong> Queensland. The study has<br />
already resulted in one publication, designating a new cosmopolitan genus and at<br />
least two species for a previously described species, Sutorius eximius and S. australianses<br />
(previously Tylopilus eximius). Further study is ongoing, providing an<br />
overview <strong>of</strong> amorphologically distinct, cosmopolitan taxon, Tylopilus chromapes,<br />
that appears to be polyphyletic based on preliminary results. An overview <strong>of</strong> additional<br />
Boletineae species occurring in Queensland, Australia and their relationships<br />
in the context <strong>of</strong> a worldwide phylogeny <strong>of</strong> Boletineae is in progress.<br />
Olarte, Rodrigo A 1 , Bruce W Horn 2 , Carolyn J Worthington 1 , and Ignazio Carbone<br />
1 . 1 Department <strong>of</strong> Plant Pathology, North Carolina State University,<br />
Raleigh, NC 27695, 2 National Peanut Research Laboratory, Agricultural Research<br />
Service, U.S. Department <strong>of</strong> Agriculture, Dawson, GA 39842. Matingtype<br />
heterokaryosis and population shifts in Aspergillus flavus<br />
Aspergillus flavus is a fungal pathogen <strong>of</strong> many agronomically important<br />
crops worldwide. We sampled A. flavus strains from a cornfield in Rocky Mount,<br />
NC. This field was planted in 2010 and plots were inoculated at tasseling with either<br />
AF36 or NRRL 21882 (=Afla-Guard) biocontrol strains, both <strong>of</strong> which are<br />
36 <strong>Inoculum</strong> <strong>63</strong>(3), June 2012<br />
mating type MAT1-2. Subsequently, toxigenic strain NRRL 3357 (MAT1-1) was<br />
applied to all plots, including control plots not inoculated with biocontrol strains.<br />
Sclerotia were harvested from infected corn ears approximately 4.5 months after<br />
planting (2.5 months after biocontrol treatment); ninety single-ascospore isolates<br />
were isolated from ascocarps originating from plots treated with AF36 and NRRL<br />
21882. In addition, eighty A. flavus isolates were collected from soil one month<br />
after planting (before biocontrol application) and one year after biocontrol application,<br />
for a grand-total <strong>of</strong> 250 isolates. Aflatoxin (AF) and cyclopiazonic acid<br />
(CPA) production were determined using standard thin-layer chromatography<br />
and HPLC. Three distinct toxin classes were identified: AF-/CPA-, AF+/CPA+<br />
and AF-/CPA+. PCR amplification revealed grouping <strong>of</strong> isolates into three distinct<br />
mating-type classes: MAT1-1, MAT1-2 and MAT1-1/MAT1-2. A significant<br />
proportion (54%) <strong>of</strong> isolates sampled prior to biocontrol treatments were heterokaryotic<br />
for mating type (MAT1-1/MAT1-2), and 39% <strong>of</strong> isolates obtained<br />
from ascospores were heterokaryotic as well as 9% <strong>of</strong> isolates from soil after biocontrol<br />
treatments. The vertical transmission <strong>of</strong> MAT1-1/MAT1-2 to progeny ascospore<br />
isolates suggests that heterokaryosis can be maintained in subsequent<br />
generations. The population genetic structure before and after the application <strong>of</strong><br />
biocontrol treatments will be discussed. Further characterization <strong>of</strong> heterokaryons<br />
and their frequency in A. flavus populations may be important in understanding<br />
the adaptation <strong>of</strong> these fungi to changing environmental conditions.<br />
Oliver, Jason P and Jonathan S Schilling. University <strong>of</strong> Minnesota, 320 Kaufert<br />
Laboratory, 2004 Folwell Avenue, St. Paul, MN 55108-6130. Manure gas eating<br />
microbes: Effect <strong>of</strong> fungal and bacterial biomass on bi<strong>of</strong>iltration <strong>of</strong> livestock<br />
production emissions<br />
Though specific data is only just being analyzed, scientists and regulators<br />
are beginning to recognize the significant emission <strong>of</strong> particulate matter, odor,<br />
hazardous and greenhouse gases from livestock production and manure management.<br />
Bi<strong>of</strong>iltration - use <strong>of</strong> a biologically active porous media to capture and degrade<br />
gaseous pollutants - is a low-cost and adaptable mitigation technology suitable<br />
for manure storage emissions. Improving the design and management <strong>of</strong><br />
bi<strong>of</strong>ilters (and ultimately adoption by producers) rests on our ability to understand<br />
the microbial ecology <strong>of</strong> the filter media, the underpinnings <strong>of</strong> bi<strong>of</strong>ilter effectiveness<br />
and efficiency. Studying bi<strong>of</strong>ilters at multiple scales, we are beginning to resolve<br />
the effect <strong>of</strong> fungal and bacterial biomass on reductions <strong>of</strong> gases generated<br />
by long-term storage <strong>of</strong> livestock manure.<br />
Orwin, Kate H 1 , Miko U F Kirschbaum 2 , Julie R Deslippe 2 , and Ian A Dickie<br />
3 . 1 Lancaster Environment Centre, Lancaster University, Lancaster, LA1 4YQ,<br />
United Kingdom, 2 Landcare Research, Private Bag 11052, Palmerston North<br />
4442, New Zealand, 3 Landcare Research, Box 40, Lincoln 7640, New Zealand.<br />
The impact <strong>of</strong> mycorrhizal fungal traits on ecosystem responses to global<br />
change: a modeling approach<br />
Ecosystems are currently being subjected to multiple global change factors,<br />
from nitrogen deposition to increasing CO2 concentrations and changes in<br />
temperature. Understanding the consequences <strong>of</strong> these effects on ecosystem<br />
processes such as carbon cycling is <strong>of</strong> prime importance, as this will determine<br />
whether ecosystems are likely to cause positive or negative feedbacks to climate<br />
change. Current evidence suggests that carbon cycling can be strongly affected by<br />
the traits <strong>of</strong> the plant community, with most studies focusing on litter quality and<br />
plant growth rates. However, recent modelling work has demonstrated that the<br />
traits <strong>of</strong> plant symbionts can also play a significant role in determining ecosystem<br />
carbon storage. In particular, the ability <strong>of</strong> mycorrhizal fungi to directly access organic<br />
nutrients can be as important as a major shift in litter quality for carbon storage.<br />
The two main mechanisms behind this effect were direct access to organic<br />
nutrients causing i) an increase in plant nutrition resulting in enhanced photosynthetic<br />
rates and subsequent carbon inputs to the soil and ii) a reduction in microbial<br />
access to nutrients, which reduced the rate <strong>of</strong> soil organic matter decomposition.<br />
We have little understanding <strong>of</strong> the way in which such interactions among<br />
mycorrhizal symbionts, their hosts and other soil decomposers may modify the effect<br />
<strong>of</strong> global change factors on ecosystem carbon dynamics. Here, we use a<br />
newly developed model (MySCaN: Mycorrhizal Status, Carbon and Nutrient cycling)<br />
to examine the impact <strong>of</strong> global change factors on carbon storage, and how<br />
these trends can be affected by mycorrhizal traits. We show that global change effects<br />
on carbon storage are not universal, but are modified by the interaction between<br />
plants and their mycorrhizal symbionts.<br />
Osmundson, Todd W and Matteo Garbelotto. Forest Mycology and Pathology<br />
Laboratory, Department <strong>of</strong> Environmental Science, Policy and Management,<br />
University <strong>of</strong> California, Berkeley, CA 94720, USA. Fire drives habitat specialization,<br />
speciation, and hybridization <strong>of</strong> Morel mushrooms in western<br />
North <strong>America</strong><br />
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