Erik Lilleskov

US Forest Service | FS · Climate, Fire, and Carbon Cycle Sciences Unit

Indonesia and Peru harbor some of the largest lowland tropical peatland areas. Indonesian peatlands are subject to much greater anthropogenic activity than Peru’s, including drainage, logging, agricultural conversion, and burning, resulting in high greenhouse gas and particulate emissions. To derive insights from the Indonesian experience, we explo...

Peatlands play a critical role in terrestrial carbon (C) storage, containing an estimated 30% of global soil C, despite occupying only 3% of global land area. Historic management of peatlands has led to widespread degradation and loss of important ecosystem services, including C sequestration. Legacy drainage features in the peatlands of northern M...

There is a data gap in our current knowledge of the geospatial distribution, type and extent of C rich peatlands across the globe. The Pastaza Marañón Foreland Basin (PMFB), within the Peruvian Amazon, is known to store large amounts of peat, but the remoteness of the region makes field data collection and mapping the distribution of peatland ecoty...

Peatlands contain a significant fraction of global soil carbon, but how these reservoirs will respond to the changing climate is still relatively unknown. A global picture of the variations in peat organic matter chemistry will aid our ability to gauge peatland soil response to climate. The goal of this research is to test the hypotheses that 1) pe...

Peatlands store one‐third of Earth’s soil carbon, the stability of which is uncertain due to climate change‐driven shifts in hydrology and vegetation, and consequent impacts on microbial communities that mediate decomposition. Peatland carbon cycling varies over steep physicochemical gradients characterizing vertical peat profiles. However, it is u...

Peatlands are found on all continents, covering 3% of the global land area. However, the spatial extent and causes of metal enrichment in peatlands is understudied and no attempt has been made to evaluate global patterns of metal enrichment in bog and fen peatlands, despite that certain metals and rare earth elements (REE) arise from anthropogenic...

Drainage‐induced encroachment by trees may have major effects on the carbon balance of northern peatlands, and responses of microbial communities are likely to play a central mechanistic role. We profiled the soil fungal community and estimated its genetic potential for the decay of lignin and phenolics (class II peroxidase potential) along peatlan...

Although wetlands contain a disproportionately high amount of earth's total soil carbon, many regions are still poorly mapped and with unquantified carbon stocks. The tropical Andes contain a high concentration of wetlands consisting mostly of wet meadows and peatlands, yet their total organic carbon stocks are poorly quantified, as well as the car...

Tropical peatlands are one of the largest natural sources of atmospheric methane (CH 4) and play a significant role in regional and global carbon budgets. However, large uncertainties persist regarding their feedbacks to climate variations. The Energy Exascale Earth System Model (E3SM) Land Model (ELM) is an ongoing state-of-the-science model, whic...

Globally, major efforts are being made to restore peatlands to maximise their resilience to anthropogenic climate change, which puts continuous pressure on peatland ecosystems and modifies the geography of the environmental envelope that underpins peatland functioning. A probable effect of climate change is reduction in the waterlogged conditions t...

Peatlands account for 15 to 30% of the world's soil carbon (C) stock and are important controls over global nitrogen (N) cycles. However, C and N concentrations are known to vary among peatlands contributing to the uncertainty of global C inventories, but there are few global studies that relate peatland classification to peat chemistry. We analyze...

A small imbalance in plant productivity and decomposition accounts for the carbon (C) accumulation capacity of peatlands. As climate changes, the continuity of peatland net C storage relies on rising primary production to offset increasing ecosystem respiration (ER) along with the persistence of older C in waterlogged peat. A lowering in the water...

High-throughput RNA sequencing offers broad opportunities to explore the Earth RNA virome. Mining 5,150 diverse metatranscriptomes uncovered >2.5 million RNA virus contigs. Analysis of >330,000 RNA-dependent RNA polymerases (RdRPs) shows that this expansion corresponds to a 5-fold increase of the known RNA virus diversity. Gene content analysis rev...

It is often difficult to compile and synthesise evidence across multiple studies to inform policy and practice because different outcomes have been measured in different ways or datasets and models have not been fully or consistently reported. In the case of peatlands, a critical terrestrial carbon store, this lack of consistency hampers the eviden...

Water table depth and vegetation are key controls of methane (CH4) emissions from peatlands. Microtopography integrates these factors into features called microforms. Microforms often differ in CH4 emissions, but microform‐dependent patterns of belowground CH4 cycling remain less clearly resolved. To investigate the impact of microtopography on bel...

Peatland ecosystems cover only 3% of the world’s land area; however, they store one-third of the global soil carbon (C). Microbial communities are the main drivers of C decomposition in peatlands, yet we have limited knowledge of their structure and function. While the microbial communities in the Northern Hemisphere peatlands are well documented,...

Northern peatlands play an important role in the global C cycle due to their large C stocks and high potential methane (CH4) emissions. The CH4 and CO2 cycles of these systems are closely linked to hydrology, with water table level regulating the balance of oxic and anoxic conditions and the water content of Sphagnum mosses that dominate primary pr...

Small genes (<150 nucleotides) have been systematically overlooked in phage genomes. We employ a large-scale comparative genomics approach to predict >40,000 small-gene families in ∼2.3 million phage genome contigs. We find that small genes in phage genomes are approximately 3-fold more prevalent than in host prokaryotic genomes. Our approach enric...

Climate change may transform peatlands from net carbon (C) sinks to C sources, which could result in a positive feedback to global warming. Warmer temperatures might lower water tables, increase the abundance of shrubs, slow Sphagnum and sedge growth and further accelerate the decomposition of dissolved organic matter (DOM) with a concomitant relea...

Páramo peatlands are a regional reservoir of biodiversity and ecosystem services, accumulating large amounts of carbon and buffering water flows. Despite their importance, they have a long history of use and impacts including drainage for agriculture and grazing, and water withdrawal for human uses. Here we present a preliminary assessment of the c...

This article is composed of three independent commentaries about the state of Integrated, Coordinated, Open, Networked (ICON) principles in the American Geophysical Union Biogeosciences section, and discussion on the opportunities and challenges of adopting them. Each commentary focuses on a different topic: (a) Global collaboration, technology tra...

Nitrogen availability frequently limits photosynthetic production in Sphagnum moss-dominated high-latitude peatlands, which are crucial carbon-sequestering ecosystems at risk to climate change effects. It has been previously suggested that microbial methane-fueled fixation of atmospheric nitrogen (N 2 ) may occur in these ecosystems, but this proce...

Many trees depend on symbiotic ectomycorrhizal fungi for nutrients in exchange for photosynthetically derived carbohydrates. Trees growing in peatlands, which cover 3% of the earth’s terrestrial surface area yet hold approximately one-third of organic soil carbon stocks, may benefit from ectomycorrhizal fungi that can efficiently forage for nutrien...

Peatland ecosystems cover only 3 % of the world’s land area, however they store one-third of the global soil carbon (C). Peatlands play a central role in global C cycling as they contain more organic C than any other terrestrial ecosystem. Microbial communities are the main drivers of C decomposition in peatlands, yet we have limited knowledge of t...

Peatlands both accumulate carbon and release methane, but their broad range in environmental conditions means that the diversity of microorganisms responsible for carbon cycling is still uncertain. Here we describe a community analysis of methanogenic archaea responsible for methane production in 17 peatlands from 36 to 53 N latitude across the eas...

Peatlands both accumulate carbon and release methane, but their broad range in environmental conditions means that the diversity of microorganisms responsible for carbon cycling is still uncertain. Here we describe a community analysis of methanogenic archaea responsible for methane production in 17 peatlands from 36 to 53 N latitude across the eas...

Peatlands play a critical role in the global carbon (C) cycle, encompassing ∼30% of the 1,500 Pg of C stored in soils worldwide. However, this C is vulnerable to climate and land-use change. Ecosystem models predict the impact of perturbation on C fluxes based on soil C pools, yet responses could vary markedly depending on soil organic matter (SOM)...

Hydrologic shifts due to climate change will affect the cycling of carbon (C) stored in boreal peatlands. Carbon cycling in these systems is carried out by microorganisms and plants in close association. This study investigated the effects of experimentally manipulated water tables (lowered, raised) and plant functional groups on the peat and root...

High-elevation peatlands in the Andes are receiving increasing attention for their biodiversity and their high rates of carbon accumulation. However, the ecology of these peatlands and the environmental factors that control their carbon dynamics remain under-studied. Here we report on the patterns of root biomass productivity and turnover rates for...

Tropical peatlands are a major, but understudied, biophysical feedback factor on the atmospheric greenhouse effect. The largest expanses of tropical peatlands are located in lowland areas of Southeast Asia and the Amazon basin. The Loreto Region of Amazonian Peru contains ~63,000 km² of peatlands. However, little is known about the biogeochemistry...

Peatlands are wetland ecosystems with great significance as natural habitats and as major global carbon stores. They have been subject to widespread exploitation and degradation with resulting losses in characteristic biota and ecosystem functions such as climate regulation. More recently, large-scale programmes have been established to restore pea...

Peatlands are important players in climate change–biosphere feedbacks via long-term net carbon (C) accumulation in soil organic matter and as potential net C sources including the potent greenhouse gas methane (CH4). Interactions of climate, site-hydrology, plant community, and groundwater chemical factors influence peatland development and functio...

Soil and the inherent biogeochemical processes in wetlands contrast starkly with those in upland forests and rangelands. The differences stem from extended periods of anoxia, or the lack of oxygen in the soil, that characterize wetland soils; in contrast, upland soils are nearly always oxic. As a result, wetland soil biogeochemistry is characterize...

Soil and the inherent biogeochemical processes in wetlands contrast starkly with those in upland forests and rangelands. The differences stem from extended periods of anoxia, or the lack of oxygen in the soil, that characterize wetland soils; in contrast, upland soils are nearly always oxic. As a result, wetland soil biogeochemistry is characterize...

Most plant diversity in temperate deciduous forests is found in the ground layer, but nearly all studies comparing plant community assembly using taxonomic-, trait-, and phylogenetic diversity indices are limited to woody plants. To examine the relationship between short-term ground-layer plant community assembly and disturbance severity, we levera...

Arbuscular mycorrhizal (AM) fungi are hypothesized to assist growth of northern white-cedar in acid peatlands, yet there is little direct evidence that they can provide sufficient resources, especially nitrogen (N), from unfertilized peat soils. Our objective was to determine mycorrhizal efficacy to support cedar growth and nutrient supply as part...

Many tropical mountain peatlands in the Andes are formed by cushion plants. These unique cushion plant peatlands are intensively utilized for grazing and are also influenced by climate change, both of which alter hydrologic conditions. Little is known about the natural hydroperiods and greenhouse gas fluxes of these peatlands or the consequences of...

Globally important carbon (C) stores in northern peatlands are vulnerable to oxidation in a changing climate. A growing body of literature draws attention to the importance of dissolved organic matter (DOM) in governing anaerobic metabolism in organic soil, but exactly how the reduction‐oxidation (redox) activities of DOM, and particularly the phen...

Climate change is expected to alter the hydrology and vascular plant communities in peatland ecosystems. These changes may have as yet unexplored impacts on peat mercury (Hg) concentrations and net methylmercury (MeHg) production. In this study, peat was collected from PEATcosm, an outdoor, controlled mesocosm experiment where peatland water table...

It is widely known that tropical peatlands, including peat swamp forests (PSFs), provide numerous ecosystem services in both spatial and temporal dimensions. These include their role as large stores for organic carbon, which when not managed well could be released as carbon dioxide and methane, accelerating climate warming. Massive destruction and...

Wetlands (called bofedales in the Andes of Peru) are abundant and important components of many mountain ecosystems across the globe. They provide many benefits including water storage, high quality habitat, pasture, nutrient sinks and transformations, and carbon storage. The remote and rugged setting of mountain wetlands creates challenges for mapp...

The extent to which ectomycorrhizal (ECM) fungi enable plants to access organic nitrogen (N) bound in soil organic matter (SOM) and transfer this growth‐limiting nutrient to their plant host, has important implications for our understanding of plant–fungal interactions, and the cycling and storage of carbon (C) and N in terrestrial ecosystems. Empi...

https://stateoftheworldsfungi.org/2018/reports/SOTWFungi_2018_Climate_Change.pdf

Humans have dramatically increased atmospheric nitrogen (N) deposition globally. At the coarsest resolution, N deposition is correlated with shifts from ectomycorrhizal (EcM) to arbuscular mycorrhizal (AM) tree dominance. At finer resolution, ectomycorrhizal fungal (EcMF) and arbuscular mycorrhizal fungal (AMF) communities respond strongly to long-...

Peatlands are a class of wetlands that are defined as having saturated soils, anaerobic conditions, and large deposits of partially decomposed organic plant material (peat). Occurring in ecozones from the tropics to the arctic, peatlands are estimated to cover just under 4.5 million km2, roughly 3–5% of the Earth’s land surface (Maltby and Proctor,...

Considerable progress has been made in ecological and evolutionary genetics with studies demonstrating how genes underlying plant and microbial traits can influence adaptation and even ‘extend’ to influence community structure and ecosystem level processes. Progress in this area is limited to model systems with deep genetic and genomic resources th...

Peatlands are widespread throughout the tropical Andean páramo. Despite the large carbon stocks in these ecosystems, carbon dioxide (CO2) and methane (CH4) flux data are lacking. In addition, cattle grazing is widespread in the páramo and could alter gas fluxes. Therefore, our objectives were to measure CO2 and CH4 fluxes with the static chamber te...