scholarly journals Diversity, taxonomic composition, and functional aspects of fungal communities in living, senesced, and fallen leaves at five sites across North America

PeerJ ◽  
2016 ◽  
Vol 4 ◽  
pp. e2768 ◽  
Author(s):  
Jana M. U’Ren ◽  
A. Elizabeth Arnold

BackgroundFungal endophytes inhabit symptomless, living tissues of all major plant lineages to form one of earth’s most prevalent groups of symbionts. Many reproduce from senesced and/or decomposing leaves and can produce extracellular leaf-degrading enzymes, blurring the line between symbiotrophy and saprotrophy. To better understand the endophyte–saprotroph continuum we compared fungal communities and functional traits of focal strains isolated from living leaves to those isolated from leaves after senescence and decomposition, with a focus on foliage of woody plants in five biogeographic provinces ranging from tundra to subtropical scrub forest.MethodsWe cultured fungi from the interior of surface-sterilized leaves that were living at the time of sampling (i.e., endophytes), leaves that were dead and were retained in plant canopies (dead leaf fungi, DLF), and fallen leaves (leaf litter fungi, LLF) from 3–4 species of woody plants in each of five sites in North America. Our sampling encompassed 18 plant species representing two families of Pinophyta and five families of Angiospermae. Diversity and composition of fungal communities within and among leaf life stages, hosts, and sites were compared using ITS-partial LSU rDNA data. We evaluated substrate use and enzyme activity by a subset of fungi isolated only from living tissues vs. fungi isolated only from non-living leaves.ResultsAcross the diverse biomes and plant taxa surveyed here, culturable fungi from living leaves were isolated less frequently and were less diverse than those isolated from non-living leaves. Fungal communities in living leaves also differed detectably in composition from communities in dead leaves and leaf litter within focal sites and host taxa, regardless of differential weighting of rare and abundant fungi. All focal isolates grew on cellulose, lignin, and pectin as sole carbon sources, but none displayed ligninolytic or pectinolytic activityin vitro. Cellulolytic activity differed among fungal classes. Within Dothideomycetes, activity differed significantly between fungi from living vs. non-living leaves, but such differences were not observed in Sordariomycetes.DiscussionAlthough some fungi with endophytic life stages clearly persist for periods of time in leaves after senescence and incorporation into leaf litter, our sampling across diverse biomes and host lineages detected consistent differences between fungal assemblages in living vs. non-living leaves, reflecting incursion by fungi from the leaf exterior after leaf death and as leaves begin to decompose. However, fungi found only in living leaves do not differ consistently in cellulolytic activity from those fungi detected thus far only in dead leaves. Future analyses should consider Basidiomycota in addition to the Ascomycota fungi evaluated here, and should explore more dimensions of functional traits and persistence to further define the endophytism-to-saprotrophy continuum.

2020 ◽  
Vol 68 (8) ◽  
pp. 473
Author(s):  
B. J. Wigley ◽  
T. Charles-Dominique ◽  
G. P. Hempson ◽  
N. Stevens ◽  
M. TeBeest ◽  
...  

Plant functional traits provide a valuable tool to improve our understanding of ecological processes at a range of scales. Previous handbooks on plant functional traits have highlighted the importance of standardising measurements of traits to improve our understanding of ecological and evolutionary processes. In open ecosystems (i.e. grasslands, savannas, open woodlands and shrublands), traits related to disturbance (e.g. herbivory, drought, and fire) play a central role in explaining species performance and distributions and are the focus of this handbook. We provide brief descriptions of 34 traits and list important environmental filters and their relevance, provide detailed sampling methodologies and outline potential pitfalls for each trait. We have grouped traits according to plant functional type (grasses, forbs and woody plants) and, because demographic stages may experience different selective pressures, we have separated traits according to the different plant life stages (seedlings saplings and adults). We have attempted to not include traits that have been covered in previous handbooks except for where updates or additional information was considered beneficial.


2021 ◽  
Vol 69 (2) ◽  
pp. 110
Author(s):  
B. J. Wigley ◽  
T. Charles-Dominique ◽  
G. P. Hempson ◽  
N. Stevens ◽  
M. te Beest ◽  
...  

Plant functional traits provide a valuable tool to improve our understanding of ecological processes at a range of scales. Previous handbooks on plant functional traits have highlighted the importance of standardising measurements of traits to improve our understanding of ecological and evolutionary processes. In open ecosystems (i.e. grasslands, savannas, open woodlands and shrublands), traits related to disturbance (e.g. herbivory, drought, and fire) play a central role in explaining species performance and distributions and are the focus of this handbook. We provide brief descriptions of 34 traits and list important environmental filters and their relevance, provide detailed sampling methodologies and outline potential pitfalls for each trait. We have grouped traits according to plant functional type (grasses, forbs and woody plants) and, because demographic stages may experience different selective pressures, we have separated traits according to the different plant life stages (seedlings saplings and adults). We have attempted to not include traits that have been covered in previous handbooks except for where updates or additional information was considered beneficial.


Forests ◽  
2021 ◽  
Vol 12 (5) ◽  
pp. 591
Author(s):  
Wensong Zhou ◽  
Yuxin Zhang ◽  
Shuang Zhang ◽  
Basil N. Yakimov ◽  
Keming Ma

Explaining community assembly mechanisms along elevational gradients dominated by deterministic processes or stochastic processes is a pressing challenge. Many studies suggest that phylogenetic and functional diversity are significant indicators of the process. In this study, we analyzed the structure and beta diversity of phylogenetic and functional traits along an elevational gradient and discussed the effects of environmental and spatial factors. We found that the phylogenetic and functional traits showed inconsistent changes, and their variations were closely related to the abiotic environment. The results suggested that the community assembly of woody plants was obviously affected by the combined effect of deterministic processes and the stochastic hypothesis (primarily by the latter). Phylogenetic and functional traits had a certain relationship but changed according to different rules. These results enhance our understanding of the assembly mechanism of forest communities by considering both phylogenetic and functional traits.


Author(s):  
P. F. Cannon

Abstract A description is provided for Protoventuria elegantula (Gibbera elegantula). This species is apparently very mildly parasitic, found initially on living leaves, but not forming lesions, later on moribund, then dead fallen leaves, also on dead fruits. Some information on its associated organisms and substrata, habitats, dispersal and transmission and conservation status is given, along with details of its geographical distribution (North America (Canada (British Columbia), USA (Washington)), Europe (Austria, Finland, Germany, Italy, Norway, Sweden, Switzerland, UK)) and hosts (Vaccinium spp.). No reports of negative economic impacts of this fungus have been found.


Author(s):  
G. S. Saddler

Abstract A description is provided for Xanthomonas fragariae. Information is included on the disease caused by the organism, its transmission, geographical distribution, and hosts. HOSTS: Fragaria × ananassa (Rosaceae); by artificial inoculation: Fragaria virginiana, F. vesca, Potentilla fruticosa and P. glandulosa (Rosaceae). DISEASE: Angular leaf spot and vascular decline or collapse of strawberry. First described in 1962 in North America. The leaf spot phase appears as minute water-soaked spots on the underside of leaves surrounded by the smallest veins. In the early stages symptoms are only visible on the leaf underside. Spots enlarge, coalesce, penetrate to the upper leaf surface and darken, turning into large, irregular necrotic areas. They have a shiny appearance and are usually covered by bacterial exudate which, when dry, turns brown and appears as gum-like scales. Spots coalesce more frequently along the primary and secondary veins. The dead tissues tear and break off, and the diseased leaf may assume a ragged appearance. Heavy losses may occur with frequent overhead sprinkler irrigation. The conditions favouring infection are moderate to cool daytime temperatures (about 20°C), low night-time temperatures and high humidities (MAAS, 1998). In addition, blossom blight of strawberry has been found in California and is caused by a complex of X. fragariae and Cladosporium cladosporioides (GUBLER et al., 1999). GEOGRAPHICAL DISTRIBUTION: AFRICA: Ethiopia, Réunion. NORTH AMERICA: Canada (New Brunswick, Newfoundland, Nova Scotia, Ontario, Quebec), USA (California, Florida, Kentucky, Minnesota, North Carolina, Wisconsin). SOUTH AMERICA: Argentina, Brazil (Minas Gerais, Rio Grande do Sul, Sao Paulo), Chile, Ecuador, Paraguay, Uruguay, Venezuela. ASIA: Taiwan, Israel. AUSTRALASIA: Australia (New South Wales, South Australia, Victoria), New Zealand. EUROPE: Belgium, France, Germany, Greece, Italy (Sicily), Netherlands, Portugal, Romania, Spain, Switzerland, Ukraine. TRANSMISSION: Rain splash from infested leaf litter in the soil on to young healthy leaves. Penetration occurs through the stomata. Infections of the crowns occur through local wounds or downwards from affected leaves. Bacteria can overwinter in leaf litter and for many years in dried leaf material. Residues of infected leaves and crown infections on runners used for planting are sources of inoculum for primary infections.


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