Novel species of fungi described in this study include those from various countries as follows: Antartica , Cladosporium austrolitorale from coastal sea sand. Australia , Austroboletus yourkae on soil, Crepidotus innuopurpureus on dead wood, Curvularia stenotaphri from roots and leaves of Stenotaphrum secundatum and Thecaphora stajsicii from capsules of Oxalis radicosa. Belgium , Paraxerochrysium coryli (incl. Paraxerochrysium gen. nov.) from Corylus avellana. Brazil , Calvatia nordestina on soil, Didymella tabebuiicola from leaf spots on Tabebuia aurea, Fusarium subflagellisporum from hypertrophied floral and vegetative branches of Mangifera indica and Microdochium maculosum from living leaves of Digitaria insularis. Canada , Cuphophyllus bondii fromagrassland. Croatia , Mollisia inferiseptata from a rotten Laurus nobilis trunk. Cyprus , Amanita exilis oncalcareoussoil. Czech Republic , Cytospora hippophaicola from wood of symptomatic Vaccinium corymbosum. Denmark , Lasiosphaeria deviata on pieces of wood and herbaceousdebris. Dominican Republic , Calocybella goethei among grass on a lawn. France (Corsica) , Inocybe corsica onwetground. France (French Guiana) , Trechispora patawaensis on decayed branch of unknown angiosperm tree and Trechispora subregularis on decayed log of unknown angiosperm tree. Germany , Paramicrothecium sambuci (incl. Paramicrothecium gen. nov.)ondeadstemsof Sambucus nigra. India , Aureobasidium microtermitis from the gut of a Microtermes sp. termite, Laccaria diospyricola on soil and Phylloporia tamilnadensis on branches of Catunaregam spinosa . Iran , Pythium serotinoosporum from soil under Prunus dulcis. Italy , Pluteus brunneovenosus on twigs of broad leaved trees on the ground. Japan , Heterophoma rehmanniae on leaves of Rehmannia glutinosa f. hueichingensis. Kazakhstan , Murispora kazachstanica from healthy roots of Triticum aestivum. Namibia , Caespitomonium euphorbiae (incl. Caespitomonium gen. nov.)from stems of an Euphorbia sp. Netherlands , Alfaria junci, Myrmecridium junci, Myrmecridium juncicola, Myrmecridium juncigenum, Ophioceras junci, Paradinemasporium junci (incl. Paradinemasporium gen. nov.), Phialoseptomonium junci, Sporidesmiella juncicola, Xenopyricularia junci and Zaanenomyces quadripartis (incl. Zaanenomyces gen. nov.), fromdeadculmsof Juncus effusus, Cylindromonium everniae and Rhodoveronaea everniae from Evernia prunastri, Cyphellophora sambuci and Myrmecridium sambuci from Sambucus nigra, Kiflimonium junci, Saro cladium junci, Zaanenomyces moderatricis academiae and Zaanenomyces versatilis from dead culms of Juncus inflexus, Microcera physciae from Physcia tenella, Myrmecridium dactylidis from dead culms of Dactylis glomerata, Neochalara spiraeae and Sporidesmium spiraeae from leaves of Spiraea japonica, Neofabraea salicina from Salix sp., Paradissoconium narthecii (incl. Paradissoconium gen. nov.)from dead leaves of Narthecium ossifragum, Polyscytalum vaccinii from Vaccinium myrtillus, Pseudosoloacrosporiella cryptomeriae (incl. Pseudosoloacrosporiella gen. nov.)fromleavesof Cryptomeria japonica, Ramularia pararhabdospora from Plantago lanceolata, Sporidesmiella pini from needles of Pinus sylvestris and Xenoacrodontium juglandis (incl. Xenoacrodontium gen. nov. and Xenoacrodontiaceae fam. nov.)from Juglans regia . New Zealand , Cryptometrion metrosideri from twigs of Metrosideros sp., Coccomyces pycnophyllocladi from dead leaves of Phyllocladus alpinus, Hypoderma aliforme from fallen leaves Fuscopora solandri and Hypoderma subiculatum from dead leaves Phormium tenax. Norway , Neodevriesia kalakoutskii from permafrost and Variabilispora viridis from driftwood of Picea abies. Portugal , Entomortierella hereditatis from abio film covering adeteriorated limestone wall. Russia , Colpoma junipericola from needles of Juniperus sabina, Entoloma cinnamomeum on soil in grasslands, Entoloma verae on soil in grasslands, Hyphodermella pallidostraminea on a dry dead branch of Actinidia sp., Lepiota sayanensis onlitterinamixedforest, Papiliotrema horticola from Malus communis , Paramacroventuria ribis (incl. Paramacroventuria gen. nov.)fromleaves of Ribes aureum and Paramyrothecium lathyri from leaves of Lathyrus tuberosus. South Africa , Harzia combreti from leaf litter of Combretum collinum ssp. sulvense, Penicillium xyleborini from Xyleborinus saxesenii , Phaeoisaria dalbergiae from bark of Dalbergia armata, Protocreopsis euphorbiae from leaf litter of Euphorbia ingens and Roigiella syzygii from twigs of Syzygium chordatum . Spain , Genea zamorana on sandy soil, Gymnopus nigrescens on Scleropodium touretii, Hesperomyces parexochomi on Parexochomus quadriplagiatus, Paraphoma variabilis from dung, Phaeococcomyces kinklidomatophilus from a blackened metal railing of an industrial warehouse and Tuber suaveolens in soil under Quercus faginea. Svalbard and Jan Mayen , Inocybe nivea associated with Salix polaris. Thailand , Biscogniauxia whalleyi oncorticatedwood. UK , Parasitella quercicola from Quercus robur. USA , Aspergillus arizonicus from indoor air in a hospital, Caeliomyces tampanus (incl. Caeliomyces gen. nov.)fromoffice dust, Cippumomyces mortalis (incl. Cippumomyces gen. nov.)fromatombstone, Cylindrium desperesense from air in a store, Tetracoccosporium pseudoaerium from air sample in house, Toxicocladosporium glendoranum from air in a brick room, Toxicocladosporium losalamitosense from air in a classroom, Valsonectria portsmouthensis from airinmen'slockerroomand Varicosporellopsis americana from sludge in a water reservoir. Vietnam , Entoloma kovalenkoi on rotten wood, Fusarium chuoi inside seed of Musa itinerans , Micropsalliota albofelina on soil in tropical evergreen mixed forest sand Phytophthora docyniae from soil and roots of Docynia indica. Morphological and culture characteristics are supported by DNA barcodes.
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This content will become publicly available on August 31, 2024
First record of plant-plant facilitative interaction from the Moscovian (Pennsylvanian, upper Carboniferous) of North China
Fallen logs acting as a seedbed for trees to aid the regeneration of vegetation is a common ecological strategy in modern forests. However, the origin, occurrence, and evolution of this nurse log strategy in the geological time is unclear. Here we report a ca. 310-millionyear-old permineralized cordaitalean tree trunk from the Moscovian (Pennsylvanian, upper Carboniferous) Benxi Formation in Yangquan City, Shanxi Province, North China, with evidence of probable cordaitalean rootlets growing inside the trunk. The specimen is interpreted as a nurse log for regeneration of cordaitaleans in coastal lowlands. It provides the first glimpse of plant-plant facilitative interaction between Pennsylvanian cordaitaleans in Cathaysia. We interpret that the Moscovian cordaitalean seedlings preferentially established on the fallen log owing to the ability of the rotting wood to store fresh water. The nurse log provided a stable substrate in an environment with episodic salinity and/or water table variations. In combination with previous records, it is suggested that a sophisticated terrestrial ecosystem with multiple interactions between plants and other organisms have developed on the central North China Craton no later than the Middle Pennsylvanian.
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- Award ID(s):
- 1714749
- NSF-PAR ID:
- 10467754
- Publisher / Repository:
- Elsevier
- Date Published:
- Journal Name:
- Palaeoworld
- ISSN:
- 1671-2412
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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We measured 10 nutrient elements in the leaves, branches and fine roots of 551 plant species growing in eight forest ecosystems in China, ranging from cold temperate to subtropical forests. We estimated the scaling relationship of multiple nutrients among plant organs at the species level and scaled‐up the relationship to the community level by combining this information with that of community structure.
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Abstract Plant interactions in extreme environments are often inferred from spatial associations and quantified by means of paired sampling. Yet, this method might be confounded by habitat‐sharing effects. Here, we address whether paired and random sampling methods provide similar results at varying levels of environmental heterogeneity. We quantified spatial associations with the two methods at three sites that encompass different micro‐environmental heterogeneity and stress levels: Mediterranean environments in Canary Islands, Spain, and Sardinia, Italy, and a cold alpine environment in Hokkaido, Japan. Then, we simulated plant communities with different levels of species micro‐habitat preferences, environmental heterogeneity, and stress levels. We found that differences in species associations between paired and random sampling were indistinguishable from zero in a homogeneous space. When simulating codispersion over a decreasing abundance gradient, both sampling methods correctly identified facilitation and distinguished it from codispersion. Yet, the pairwise method provided higher facilitation estimates than the random one. At each site, there were strong differences between beneficiary species in their spatial association with nurse species, and associations became more positive with increasing stress in Spain. Most importantly, there were no differences in results yielded by the two methods at any of the different stress levels at the Spanish and Japanese sites. At the Italian site, although micro‐environmental heterogeneity was low, we found weakly significant differences between methods that were unlikely due to habitat‐sharing effects. Thus, the paired sampling method can provide significant insights into net and long‐term effects of plant interactions in spatially conspicuous environments.
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Alday, Josu (Ed.)Abstract Question Nurse–beneficiary plant interactions are often used to restore degraded habitats. However, whether and how shifts in plant–plant interactions along the facilitation–competition continuum alter revegetation success has been seldom considered. To test whether and how shifts in plant–plant interactions (due to woody species identity, study site, early life stage, and individual nurse) might alter plant recruitment and thus the success of revegetation projects, we chose a system comprising the Mediterranean dwarf palm ( Chamaerops humilis ) and seven common woody plant species. Location Two human‐degraded sites within Doñana National Park (southwestern Spain). Methods We carried out several well‐replicated field experiments to compare plant performance (seed survival, seedling emergence, seedling survival, seedling recruitment) in the presence and absence of Chamaerops humilis . Results Chamaerops humilis had marked effects on the performance of woody species that, however, changed among life stages. Depending on woody species identity, seed survival was up to 193 times greater in adjacent open spaces than beneath Chamaerops humilis . Conversely, seedling survival and recruitment were up to 19 times greater beneath Chamaerops humilis than in open spaces. Importantly, none of the studied woody species showed greater accumulated recruitment in open spaces than beneath Chamaerops humilis . Interestingly, we found strong inter‐individual palm variation in the sign and strength of their effect on woody plant performance. Conclusions We found strong seed–seedling conflicts the strength of which was species‐specific. The strong inter‐individual palm variation depicts a facilitation–competition continuum with important implications for restoration. We propose several management recommendations across different hierarchical levels (i.e., from individuals to communities) that may increase plant recruitment and therefore the success of revegetation projects. Our results are particularly relevant for restoring arid, semi‐arid and alpine landscapes worldwide where the nurse–beneficiary plant interactions are critical to ameliorating stressful conditions.more » « less
