Gerard C. Adams
Michigan State University
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Featured researches published by Gerard C. Adams.
American Journal of Botany | 2002
Stephen D. Davis; Frank W. Ewers; John S. Sperry; Kimberly A. Portwood; Michelle C. Crocker; Gerard C. Adams
Progressive diebacks of outer canopy branchlets of Ceanothus crassifolius were repeatedly observed after rainless periods up to 9 mo in duration in the Santa Monica Mountains of southern California. Mean xylem pressures of branchlets near the end of drought were as low as -11.2 MPa (N = 22) with a mean of about 60 dead branchlets per shrub. Inoculation (N = 15) with three species of fungi previously isolated from the same population of C. crassifolius did not promote dieback, suggesting that the observed decline was not fungal induced, as had been proposed. Further, at least 50% of healthy-appearing twigs, without symptoms of dieback, contained isolatible endophytic fungi. We used a centrifugal force method to determine the range of xylem pressure causing cavitation (vulnerability curves) for branchlets (N = 12) and roots (N = 16). We combined vulnerability curves with soil texture data (N = 6) into a water transport model that estimated the critical values (P(Lcrit)) of leaf xylem pressure associated with the loss of water from soil to foliage. Maximum P(Lcrit) was between -10 and -11 MPa and within the range of minimum measured xylem pressures of branchlets during drought and dieback. Branchlet dieback correlated with seasonal declines in xylem pressure in concert with declining safety margins from hydraulic failure. Symptoms of dieback were duplicated in the field by partially severing stem xylem that normally supplied branchlets with water. Taken together, these results indicate that loss of hydraulic conductance to foliage was the probable cause of the observed dieback in C. crassifolius. Partial dieback of peripheral branchlets, and its attendant reduction in evaporative surface area, may be a last-resort mechanism for whole-plant water conservation and drought survival in this species.
Rapid Communications in Mass Spectrometry | 2008
Robin Sutka; Gerard C. Adams; Nathaniel E. Ostrom; Peggy H. Ostrom
Identifying the importance of fungi to nitrous oxide (N2O) production requires a non-intrusive method for differentiating between fungal and bacterial N2O production such as natural abundance stable isotopes. We compare the isotopologue composition of N2O produced during nitrite reduction by the fungal denitrifiers Fusarium oxysporum and Cylindrocarpon tonkinense with published data for N2O production during bacterial nitrification and denitrification. The fractionation factors for bulk nitrogen isotope values for fungal denitrification were in the range -74.7 to -6.6 per thousand. There was an inverse relationship between the absolute value of the fractionation factors and the reaction rate constant. We interpret this in terms of variation in the relative importance of the rate constants for diffusion and enzymatic reduction in controlling the net isotope effect for N2O production during fungal denitrification. Over the course of nitrite reduction, the delta(18)O values for N2O remained constant and did not exhibit a relationship with the concentration characteristic of an isotope effect. This probably reflects isotopic exchange with water. Similar to the delta(18)O data, the site preference (SP; the difference in delta(15)N between the central and outer N atoms in N2O) was unrelated to concentration during nitrite reduction and, therefore, has the potential to act as a conservative tracer of production from fungal denitrification. The SP values of N2O produced by F. oxysporum and C. tonkinense were 37.1 +/- 2.5 per thousand and 36.9 +/- 2.8 per thousand, respectively. These SP values are similar to those obtained in pure culture studies of bacterial nitrification but quite distinct from SP values for bacterial denitrification. The large magnitude of the bulk nitrogen isotope fractionation and the delta(18)O values associated with fungal denitrification are distinct from bacterial production pathways; thus multiple isotopologue data holds much promise for resolving bacterial and fungal production. Our work further provides insight into the role that fungal and bacterial nitric oxide reductases have in determining site preference during N2O production.
Fungal Biology | 2003
Heather E. Hallen; Roy Watling; Gerard C. Adams
Conocybe lactea was examined as part of a larger study on the distribution of amatoxins and phallotoxins in fungi, and the taxonomic relationships between these fungi. As amatoxins are present in the congener C. filaris, the locally abundant C. lactea was examined using HPLC and mass spectroscopy. Amatoxins were not found in C. lactea, but the related phallotoxins were present in small quantities making it the first fungus outside of the genus Amanita in which phallotoxins have been detected. Despite the presence of a related toxin, C. lactea was found not to be taxonomically close to C. filaris. Phylogenetic analyses using nuclear ribosomal RNA genes indicated that North American specimens of C. lactea were conspecific with North American specimens of C. crispa in Conocybe sect. Candidae. European C. crispa was a distinct taxon. The implications of the use of the name C. albipes for these taxa are discussed. Nucleotide data confirmed placement of the sequestrate taxon Gastrocybe lateritia in sect. Candidae, but as a distinct taxon. It is hypothesized that the unique sequestrate morphology of G. lateritia may be caused by a bacterial infection.
Experimental Mycology | 1987
Gerard C. Adams; Nancy Johnson; John F. Leslie; L. Patrick Hart
Abstract Heterokaryosis in Gibberella zeae varies depending upon the compatibility of the fused strains and the manner in which the strains are fused. Analysis of nutritionally complementing auxotrophic markers in pairings via hyphal anastamoses revealed a nuclear distribution in which heterokaryosis was restricted to anastamosed cells; apical cells remained auxotrophic but both types of nuclei could be recovered from multinucleate macroconidia. A comparable pairing via protoplast fusion yielded, initially, a fusion product in which apical cells were prototrophic and the conidia contained only one nuclear type. Analysis of subcultures of this fusion product, however, revealed a change. As in the heterokaryon generated by hyphal anastomoses, apical cells were auxotrophic and both types of nucleic could be found in the conidia. Heterokaryons could not be established by pairing vegetatively incompatible hyphal cells but the fusion of protoplasts from incompatible cells yielded a slow-growing, prototrophic colony in which conidia resolved only one nuclear type. This nuclear type was different from either of the parental types, and all conidia were capable of growth on minimal medium. The complementing nuclear types were not recovered. Protoplast fusion between vegetatively incompatible strains (G. zeae Types A and B) apparently produced a heteroploid.
Phytopathology | 2013
Jaime Aguayo; Gerard C. Adams; Fabien Halkett; Mursel Catal; Claude Husson; Zoltán Nagy; Everett Hansen; Benoit Marçais; Pascal Frey
Alder decline caused by Phytophthora alni has been one of the most important diseases of natural ecosystems in Europe during the last 20 years. The emergence of P. alni subsp. alni -the pathogen responsible for the epidemic-is linked to an interspecific hybridization event between two parental species: P. alni subsp. multiformis and P. alni subsp. uniformis. One of the parental species, P. alni subsp. uniformis, has been isolated in several European countries and, recently, in North America. The objective of this work was to assess the level of genetic diversity, the population genetic structure, and the putative reproduction mode and mating system of P. alni subsp. uniformis. Five new polymorphic microsatellite markers were used to contrast both geographical populations. The study comprised 71 isolates of P. alni subsp. uniformis collected from eight European countries and 10 locations in North America. Our results revealed strong differences between continental populations (Fst = 0.88; Rst = 0.74), with no evidence for gene flow. European isolates showed extremely low genetic diversity compared with the North American collection. Selfing appears to be the predominant mating system in both continental collections. The results suggest that the European P. alni subsp. uniformis population is most likely alien and derives from the introduction of a few individuals, whereas the North American population probably is an indigenous population.
Archive | 1996
Gerard C. Adams
The genetics of Rhizoctonia solani and related species is complex and remains poorly understood. When R. solani was first studied it was apparent that it was a ubiquitous species, that it could parasitize an enormous host range, and that it occurred in a great variety of cultural forms. The scientific community actively sought an understanding of what mechanisms underlay the organisms successful and broad adaptations as a pathogen. But an understanding did not come easily and I believe that in large part this was due to our confusion in whether to view the organism as a functionally sexual or functionally asexual (non-sexual) species.
Mycologia | 1982
Z. K. Punja; R. G. Grogan; Gerard C. Adams
Forty-two isolates of Sclerotium rolfsii from California were grown on eight media to determine nutritional conditions promoting formation of the teleomorph (Athelia rolfsii). Most of the isolates (71%) formed hymenia on PDA containing 2% activated charcoal (C-PDA). Of an additional 34 isolates from areas other than California, 17 also fruited on this medium. The extent of hymenial formation on C-PDA was influenced by the conditions of incubation and the isolate. Best results were obtained when 6 or 8 mm diam mycelial plugs taken from 8- to 10-da-old PDA cultures were used as inocula, and when dishes were incubated for 4-5 wk at 24-28 C and low light intensities. Transfer of mycelial plugs from a nutrient-rich medium, e.g., PDA, to one poorer in nutrients, e.g., Browns medium or dilute PDA, induced fruiting in certain isolates. In general, nutritional or environmental conditions that restricted optimal growth and sclerotial production by the fungus favored hymenial formation. The salient features of the development and structure of the basidiocarp are described and illustrated. The teleomorph of the plant pathogenic fungus Sclerotium rolfsii Sacc. was first described by Goto (9) who provisionally placed it in Corticium centrifugum (Lev.) Bres. Curzi (5) later proposed that C. rolfsii should be designated as the basidial state of S. rolfsii. The teleomorph was transferred to Pellicularia by West (22), and subsequently placed in Botryobasidiulm by Venkatarayan (21). Talbot in 1973 (19) suggested that the basidial state of S. rolfsii belonged to the genus Athelia, and acting upon his suggestion, Tu and Kimbrough (20) made the combination A. rolfsii. We accept A. rolfsii (Curzi) Tu and Kimbrough as the name for the teleomorph. The teleomorph of S. rolfsii has been reported infrequently from nature (11, 22), but there are some reports of hymenial formation in culture (1, 9, 14, 15). However, in most studies, observations of fruiting have been incidental. Most workers, with the exception of Goto (10, 11) and Kulkarni and co-workers (1, 13), reported hymenial formation in two or three isolates grown on one or two media. Possible differences between isolates in their ability to fruit and the influence of media on hymenial formation, were not investigated. Moreover, the conditions that promoted formation of the basidiocarp in different isolates of S. rolfsii were never clearly described. There are few published light micrographs and no scanning electron micrographs of the teleomorph, and adequate descriptions of the development and structure of the basidiocarp are lacking, thus making identification difficult. This study was undertaken to establish the nutritional and environmental conditions that induce hymenial formation in isolates of S. rolfsii and to describe the development and structure of the basidiocarp. Seventy-six isolates from various hosts and geographical areas were tested. Media used by other workers, and additional media developed in this study, were employed. The conditions that
Persoonia | 2012
Pedro W. Crous; Roger G. Shivas; Michael J. Wingfield; Brett A. Summerell; Amy Y. Rossman; Janaina L. Alves; Gerard C. Adams; Robert W. Barreto; A. Bell; M.L. Coutinho; S.L. Flory; Genevieve M. Gates; K.R. Grice; Giles E. St. J. Hardy; N.M. Kleczewski; Lorenzo Lombard; C.M.O. Longa; Gerry Louis-Seize; F. Macedo; D.P. Mahoney; G. Maresi; Pedro M. Martin-Sanchez; Ludmila Marvanová; Andrew M. Minnis; Luis N. Morgado; Machiel E. Noordeloos; Alan J. L. Phillips; W. Quaedvlieg; Peter G. Ryan; C. Saiz-Jimenez
Novel species of microfungi described in the present study include the following from Australia: Catenulostroma corymbiae from Corymbia, Devriesia stirlingiae from Stirlingia, Penidiella carpentariae from Carpentaria, Phaeococcomyces eucalypti from Eucalyptus, Phialophora livistonae from Livistona, Phyllosticta aristolochiicola from Aristolochia, Clitopilus austroprunulus on sclerophyll forest litter of Eucalyptus regnans and Toxicocladosporium posoqueriae from Posoqueria. Several species are also described from South Africa, namely: Ceramothyrium podocarpi from Podocarpus, Cercospora chrysanthemoides from Chrysanthemoides, Devriesia shakazului from Aloe, Penidiella drakensbergensis from Protea, Strelitziana cliviae from Clivia and Zasmidium syzygii from Syzygium. Other species include Bipolaris microstegii from Microstegium and Synchaetomella acerina from Acer (USA), Brunneiapiospora austropalmicola from Rhopalostylis (New Zealand), Calonectria pentaseptata from Eucalyptus and Macadamia (Vietnam), Ceramothyrium melastoma from Melastoma (Indonesia), Collembolispora aristata from stream foam (Czech Republic), Devriesia imbrexigena from glazed decorative tiles (Portugal), Microcyclospora rhoicola from Rhus (Canada), Seiridium phylicae from Phylica (Tristan de Cunha, Inaccessible Island), Passalora lobeliae-fistulosis from Lobelia (Brazil) and Zymoseptoria verkleyi from Poa (The Netherlands). Valsalnicola represents a new ascomycete genus from Alnus (Austria) and Parapenidiella a new hyphomycete genus from Eucalyptus (Australia). Morphological and culture characteristics along with ITS DNA barcodes are also provided.
Mycologia | 2002
Gerard C. Adams; Rupa S. Surve-Iyer; Amy F. Iezzoni
Leucostoma species that are the causal agents of Cytospora canker of stone and pome fruit trees were studied in detail. DNA sequence of the internal transcribed spacer regions and the 5.8S of the nuclear ribosomal DNA operon (ITS rDNA) supplied sufficient characters to assess the phylogenetic relationships among species of Leucostoma, Valsa, Valsella, and related anamorphs in Cytospora. Parsimony analysis of the aligned sequence divided Cytospora isolates from fruit trees into clades that generally agreed with the morphological species concepts, and with some of the phenetic groupings (PG 1-6) identified previously by isozyme analysis and cultural characteristics. Phylogenetic analysis inferred that isolates of L. persoonii formed two well-resolved clades distinct from isolates of L. cinctum. Phylogenetic analysis of the ITS rDNA, isozyme analysis, and cultural characteristics supported the inference that L. persoonii groups PG 2 and PG 3 were populations of a new species apparently more genetically different from L. persoonii PG 1 than from isolates representative of L. massariana, L. niveum, L. translucens, and Valsella melastoma. The new species, L. parapersoonii, was described. A diverse collection of isolates of L. cinctum, L. persoonii, and L. parapersoonii were examined for genetic variation using restriction fragment length polymorphism (RFLP) analysis of the ITS rDNA and the five prime end of the large subunit of the rDNA (LSU rDNA). HinfI and HpaII endonucleases were each useful in dividing the Leucostoma isolates into RFLP profiles corresponding to the isozyme phenetic groups, PG 1-6. RFLP analysis was more effective than isozyme analysis in uncovering variation among isolates of L. persoonii PG 1, but less effective within L. cinctum populations. Isolates representative of seven of the L. persoonii formae speciales proposed by G. Défago in 1935 were found to be genetically diverse isolates of PG 1. Two large insertions, 415 and 309 nucleotides long, in the small subunit (SSU) of the nuclear rDNA of L. cinctum were identified as Group 1 introns; intron 1 at position 943 and intron 2 at position 1199. The two introns were found to be consistently present in isolates of L. cinctum PG 4 and PG 5 and absent from L. cinctum PG 6 isolates, despite the similarity of the ITS sequence and teleomorph morphology. Intron 1 was of subgroup 1C1 whereas intron 2 was of an unknown subgroup. RFLP patterns and presence/absence of introns were useful characters for expediting the identification of cultures of Leucostoma isolated from stone and pome fruit cankers. RFLP patterns from 13 endonucleases provided an effective method for selecting an array of diverse PG 1 isolates useful in screening plant germplasm for disease-resistance.
IMA fungus | 2015
Amy Y. Rossman; Gerard C. Adams; Paul F. Cannon; Lisa A. Castlebury; Pedro W. Crous; Marieka Gryzenhout; Walter M. Jaklitsch; Luis C. Mejía; Dmitar Stoykov; Dhanushka Udayanga; Hermann Voglmayr; Donald M. Walker
In advancing to one name for fungi, this paper treats generic names competing for use in the order Diaporthales (Ascomycota, Sordariomycetes) and makes a recommendation for the use or protection of one generic name among synonymous names that may be either sexually or asexually typified. A table is presented that summarizes these recommendations. Among the genera most commonly encountered in this order, Cytospora is recommended over Valsa and Diaporthe over Phomopsis. New combinations are introduced for the oldest epithet of important species in the recommended genus. These include Amphiporthe tiliae, Coryneum lanciforme, Cytospora brevispora, C. ceratosperma, C. cinereostroma, C. eugeniae, C. fallax, C. myrtagena, Diaporthe amaranthophila, D. annonacearum, D. bougainvilleicola, D. caricae-papayae, D. cocoina, D. cucurbitae, D. juniperivora, D. leptostromiformis, D. pterophila, D. theae, D. vitimegaspora, Mastigosporella georgiana, Pilidiella angustispora, P. calamicola, P. pseudogranati, P. stromatica, and P. terminaliae.