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Gewirtzman, J.

Publications and source records attributed to Gewirtzman, J..

6 recordsLinked to original sources

Internal decay in living trees: a quantitative tomography framework and its application in a temperate forest

Internal decay in living trees is an important component of carbon and nutrient cycling as well as species and structural diversity maintenance in forest ecosystems. We used sonic and electrical resistance tomography to evaluate and compare the prevalence and severity of stem decay in 57 living trees among four common species (Acer rubrum L., Nyssa sylvatica Marsh., Quercus rubra L., and Tsuga canadensis (L.) Carriere)) with overlapping and non-overlapping distributions across wetland and upland habitat types at the Harvard Forest in Petersham, MA, USA. Independent of tree size, site identity best explained variation in the prevalence of decay across trees sampled, whereas species identity best explained the severity of decay. We categorized trees as having no decay, incipient decay, active decay, or cavities based on combined sonic and electrical resistance metrics, the latter generated by a custom image analysis application. About 31% of wetland trees exhibited incipient decay (compared to 11% in the upland), whereas about 32% of upland trees exhibited active decay (compared to 10% in the wetland). Our study highlights a new quantitative framework for decay categorization through normalized principal component analysis (PCA) and decay analysis software that complements dual tomographic methodology for future investigations of ecological drivers of decay presence and susceptibility.

ecology↗

Contrasting controls on tree methane emissions in upland and wetland forests

Trees can produce, consume, transport, and emit methane (CH), yet the environmental controls and mechanisms underlying these fluxes remain poorly understood. We combined 1,640 stem-chamber observations (2023-2025) with tower-based meteorology, soil moisture and temperature networks, water table monitoring, and non-destructive tomography to test how hydrology, energy balance, species identity, and internal wood condition regulate stem CH flux. Wetland trees emitted approximately 40-fold more CH than upland trees (1.96 vs. 0.05 nmol m-{superscript 2} s-{superscript 1}). At the wetland, a three-way interaction between soil temperature, water table depth, and species explained 65% of flux variance, consistent with soil-derived CH transport through stems. The wetland specialist Nyssa sylvatica emitted an order of magnitude more CH than co-occurring generalists, likely reflecting flood-tolerance adaptations that enhance gas transport. In contrast, upland fluxes showed minimal environmental control (R{superscript 2} < 9%), with most variance occurring as unexplained temporal variation within individual trees--a pattern suggesting competing methanogenic and methanotrophic processes operating near equilibrium. Internal wood condition, assessed via acoustic and electrical resistance tomography, had opposite effects across sites: decay increased emissions in upland trees, likely by creating anaerobic microsites for in situ production, while decay decreased net emissions in wetland trees, likely by impairing transport of soil-derived CH more than it enhanced in situ production. Together, these results indicate that the dominant controls on tree CH flux differ fundamentally between wetland and upland forests, underscoring the need to represent hydrologic setting, species composition, and tree condition when scaling forest CH contributions to regional budgets.

ecology↗

Tree microbiomes and methane emissions in upland forests

RationaleUpland forest trees emit CH , but whether emissions derive from internal microbial production or soil-derived transport remains debated. Methanogens have been detected in heartwood of several species, yet the prevalence of wood-associated methanogenesis, its metabolic basis, and its relationship to co-occurring methanotrophy are poorly understood. MethodsWe measured 1,148 stem fluxes and 276 soil fluxes, sampled internal stem gases including {delta}{superscript 1}3CH , quantified methanogens and methanotrophs via ddPCR in 564 samples, characterized communities via 16S rRNA sequencing, and upscaled fluxes. Key resultsMethanogens were detected in 97% of heartwood samples (up to 10 copies g {superscript 1}) at concentrations exceeding soil by [~]2 orders of magnitude; methane consumers were likewise near-ubiquitous across forest compartments. Wood harbored distinct microbial communities dominated by hydrogenotrophic Methanobacteriaceae, corroborated by depleted {delta}{superscript 1}3CH . Vertical flux profiles indicated soil transport only in wet microsites, with uniform emissions across height consistent with internal production across most upland species. Species-level methanogen:methanotroph ratios predicted emissions (R{superscript 2} = 0.51), indicating net flux reflects the balance between production and oxidation. Main conclusionMethane-cycling microbes are widespread in upland trees, and net methane flux reflects the species-level balance between production and consumption. Internal methanogenesis contributes widely to upland tree emissions; resolving ecosystem-scale magnitude requires improved quantification of woody surface area and vertical flux variability.

ecology↗

A diverse and distinct microbiome inside living trees

Despite significant advances in microbiome research across various environments1, the microbiome of Earths largest biomass reservoir- the wood of living trees2- remains largely unexplored. This oversight neglects a critical aspect of global biodiversity and potentially key players in tree health and forest ecosystem functions. Here we illuminate the microbiome inhabiting and adapted to wood, and further specialized to individual host species. We demonstrate that a single tree can host approximately a trillion microbes in its aboveground internal tissues, with microbial communities partitioned between heartwood and sapwood, each maintaining a distinct microbiome with minimal similarity to other plant tissues or nearby ecosystem components. Notably, the heartwood microbiome emerges as a unique ecological niche, distinguished in part by endemic archaea and anaerobic bacteria that drive consequential biogeochemical processes. Our research supports the emerging idea of a plant as a "holobiont"3,4--a single ecological unit comprising host and associated microorganisms--and parallels human microbiome research in its implications for host health, disease, and functionality5. By mapping the structure, composition, and potential sources and functions of the tree internal microbiome, our findings pave the way for novel insights into tree physiology and forest ecology, and establish a new frontier in environmental microbiology.

ecology↗

A Method for Sampling the Living Wood Microbiome

Efforts to characterize microbial life across diverse environments have progressed tremendously, yet the microbiome of Earths largest biomass reservoir--the wood of living trees--has been largely unexplored. Current understanding of the tree microbiome is largely confined to roots and leaves, with little attention given to the endophytic microbiome of wood, even though emergent studies have indicated this zone as a niche for unique taxa, of consequence for ecosystem health and global biogeochemical cycles. The lack of investigation derives partly from the physical recalcitrance of wood, which presents challenges during sampling, homogenization, and the extraction of nucleic acids. In response to these issues, we present an optimized method for processing wood for use in microbial analyses, from sampling through to downstream analyses. Using methane-cycling taxa as model endophytes, we assess losses in recovery during our method, and determine a limit-of-detection of approximately 500 cells per 100 mg of (dry) wood. For all six species evaluated--which represented several diverse taxa of hardwoods and softwoods--PCR inhibition proved minimal, and we expect this method to be applicable for a majority of tree species. The methods presented herein can facilitate future investigation into the wood microbiome and global microbial ecology of methane cycling.

ecology↗

Multi-scale observations of mangrove blue carbon fluxes; the NASA Carbon Monitoring System BlueFlux field campaign

The BlueFlux field campaign is supported by NASAs Carbon Monitoring System (CMS) and will develop prototype blue carbon products to inform coastal carbon management. Blue carbon is included in carbon-dioxide removal actions proposed to reduce atmospheric CO2 concentrations to mitigate climate change. Due to their high productivity and carbon storage, combined with historic losses and a wide-range of beneficial ecosystem services, the restoration and conservation of mangrove ecosystems features prominently in blue-carbon planning. The goal of BlueFlux is to carry out multi-scale measurements of CO2 and CH4 fluxes using chambers, flux towers, and aircraft and scale these to gridded products using space-based observations of forest structure and surface reflectance. The measurements cover gradients in disturbance, mainly from the history of hurricanes in the region that drive the dieback of mangroves and the formation of ghost forests. The fluxes of CH4 emissions will be contrasted with CO2 uptake to provide a more complete budget of radiative forcing and to understand the net climate benefits of blue carbon. BlueFlux demonstrates that quantifying the removals of CO2 and emissions of CH4 using a multi-scale approach can provide increased confidence in regional greenhouse-gas accounting, contribute to process-understanding, and help inform restoration and conservation efforts in the context of climate mitigation.

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