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36 results for “decay rates”
Interactions between plants and fungi and their roles in decay rates and CO2 release in five tropical leaf species
A microcosm experiment was used to test for the effects of interactions between particular plant and fungal decomposer species on rates of leaf decomposition. Each microcosm contained one species of leaf that was sterilized with gamma irradiation and then inoculated with a single fungus. Five plant species and ten fungal species (two dominants from each of the litter types) were used in all possible combinations. Plant species were selected for pair-wise comparisons based on phylogenetic relationships and litter quality characteristics. Decomposition was measured by both mass loss and CO2 release. Differences in weight loss and CO2 evolution were highly significant for plants, fungal species, and their interactions. Mass loss was positively correlated with CO2 evolution. Contrary to our hypotheses, however, microfungal dominants did not decompose their source leaves faster than microfungal dominants from other leaf species, nor were responses to other types of specificity detected. Matching of fungi to leaf substrates by their source, by phylogenetic relationships, or by chemical, physical and structural characteristics was not associated with consistent increases in decomposition. Although previously documented differences in microfungal species composition and dominance among decomposing leaves of different trees were confirmed in this study, such differences apparently do not directly affect the rates of ecosystem processes. The presence in a few of the microcosms of a generalist basidiomycete that had ligninolytic enzymes, Melanotus eccentricus, significantly accelerated the rate of decomposition. Non-specific basidiomycetes may therefore have a stronger effect on early stages of leaf litter decomposition than host-selective microfungi. Support for this work was provided by grants BSR-8811902, DEB-9411973, DEB-9705814 , DEB-0080538, DEB-0218039 , DEB-0620910 , DEB-1239764, DEB-1546686, and DEB-1831952 from the National Science Foundation to the University of Pue
Dissolved oxygen decay rate and ambient condition data, Waccamaw River Watershed, SC, Summer 2020
Ambient conditions of various dissolved and particulate biogeochemical parameters were measured within replicate station types (Waccamaw River proper, stormwater detention ponds, and forested wetlands) within the watershed of the Waccamaw River, SC in the summer of 2020. Additionally, 5-day dark bottle incubations of dissolved oxygen allowed the calculation of decay rates using an exponential curve fit. Q10 temperature coefficients were calculated using...
Ambient nutrients, carbon, and DOM absorbance metrics along with experimental dissolved oxygen decay rates for 5-day incubations of water within the Waccamaw River Watershed, SC, Summer 2020.
Dissolved oxygen (DO) impairment within coastal waters is widespread. Rising temperatures may exacerbate low DO levels by enhancing organic matter (OM) degradation. Here, the temperature sensitivity of OM degradation was investigated as DO decay rates determined during standard five-day biochemical oxygen demand (BOD) measurements conducted under different incubation temperatures. Sampling was conducted in the Waccamaw River watershed, South Carolina, a blackwater river with extensive forested wetland that also receives drainage from stormwater detention ponds associated with coastal development, thus providing contrasting sources of OM composition. Temperature sensitivities were measured as Q10 temperature coefficients, which define how DO decay rates change with 10 degrees of warming. The average Q10 value for the wetland sites (2.14 ± 0.41) was significantly greater (p = 0.004) than those measured in either the river (1.49 ± 0.36) or stormwater ponds (1.41 ± 0.21). Furthermore, using Intergovernmental Panel on Climate Change intermediate-to-very high temperature estimates for 2100 of +2.7 – 4.4 °C, average predicted increases in DO decay rates for wetlands (~22-39 %) are more than double the River (~11-18 %) and stormwater pond rates (~9-16 %). Our findings for inland, coastal waters agree with previous results for soils, suggesting that temperature sensitivities are variable across sites and increase with more complex, lower quality OM. Future modeling scenarios of DO utilization must therefore consider the influence of OM heterogeneity and the temperature sensitivity response of OM degradation across sources and region to better predict how climate change may impact oxygen impairment in aquatic ecosystems.
Methodology matters for comparing coarse wood and bark decay rates across tree species
<p>1. The importance of wood decay for the global carbon and nutrient cycles is widely recognized. However, relatively little is known about bark decay dynamics, even though bark represents up to 25% of stem dry mass. Moreover, bark presence versus absence can significantly alter wood decay rates. Therefore, it really matters for the fate of carbon whether variation in bark and wood decay rates is coordinated across tree species.</p> <p>2. Answering this question requires advances in methodology to measure both bark and wood mass loss accurately. Decay rates of large logs in the field are often quantified as loss in tissue density, in which case volume depletions of bark and wood can give large underestimations.</p> <p>3. To quantify the real decay rates, we assessed bark mass loss per stem surface area and wood mass loss based on volume-corrected density loss. We further defined the range of actual bark mass loss by considering bark cover loss. Then, we tested the correlation between bark and wood mass loss across 20 temperate tree species during 4 years of decomposition.</p> <p>4. The area-based method generally showed more than 3-fold higher bark mass loss than the density-based method (even higher if considering bark cover loss), and volume-corrected wood mass losses were 1.08-1.12 times higher than density-based mass loss. The deviation of bark mass loss between the two methods was higher for tree species with thicker inner bark. Bark generally decomposed twice as fast as wood across species, and faster decaying bark came with faster decaying wood (R2=0.26, P=0.006).</p> <p>5. We strongly suggest using corrected volume when assessing wood mass loss especially for the species with faster decomposable sapwood and all the wood at advanced decay stages. Further studies of coarse stem decomposition should consider trait "afterlife" effects of inner bark and estimate fraction of stem bark cover to obtain more accurate decay rates. 6. Our new method should benefit our understanding of the in situ dynamics of woody debris decay and monitoring research in different forest ecosystems worldwide, and should aid meta-analyses across diverse studies.</p>
Supplementary material S19: The growth and decay rate of the Varroa jolting pulse.
<p>The growth and decay of the <em>Varroa </em>jolting pulse on each of the three substrates. Panel ‘a’ showcases the loudest jolting pulse waveform registered on honeycomb, and panel ‘b’ showcases the loudest jolting pulse waveform registered on petri-dish, both of which demonstrate an exponential growth and decay that is highlighted within the red envelope. The growth rate and decay constant were estimated visually (honeycomb growth rate = 0.05ms, honeycomb decay constant = 0.1ms, petri-dish growth rate = 0.09ms, petri-dish decay constant = 1.2ms). The growth rate is the only element of the waveform that is caused by the animal, the decay constant on both the honeycomb and petri-dish are likely the result of the response of the substrate. The brood-comb <em>Varroa </em>jolting pulse seen in panel ‘c’ is the result of the averaged accelerometer waveform for the 40 jolting pulses deemed to be loudest, and are shown in panel ‘d’ to have an envelope following a gaussian function. All peaks in the vibrational trace were forced to become positive values to demonstrate the gaussian function. The negligible exponential decay can be seen, beginning at approximately 3.9ms.</p>
Particle size influences decay rates of environmental DNA in aquatic systems
<p>Environmental DNA (eDNA) analysis is a powerful tool for remote detection of target organisms. However, obtaining quantitative and longitudinal information from eDNA data is challenging, requiring a deep understanding of eDNA ecology. Notably, if the various size components of eDNA decay at different rates, and we can separate them within a sample, their changing proportions could be used to obtain longitudinal dynamics information on species. To test this possibility, we conducted an aquatic mesocosm experiment in which we separated fish-derived eDNA components using sequential filtration to evaluate the decay rate and changing proportion of various eDNA particle sizes over time. We then fit four alternative mathematical decay models to the data, building towards a predictive framework to interpret eDNA data from various particle sizes. We found that medium-sized particles (1-10 μm) decayed more slowly than other size classes (i.e., <1 μm and >10 μm), and thus made up an increasing proportion of eDNA particles over time. We also observed distinct eDNA particle size distribution (PSD) between our Common carp and Rainbow trout samples, suggesting that target-specific assays are required to determine starting eDNA PSDs. Additionally, we found evidence that different sizes of eDNA particles do not decay independently, with particle size conversion replenishing smaller particles over time. Nonetheless, a parsimonious mathematical model where particle sizes decay independently best explained the data. Given these results, we suggest a framework to discern target distance and abundance with eDNA data by applying sequential filtration, which theoretically has both metabarcoding and single-target applications.</p>
Particle size influences decay rates of environmental DNA in aquatic systems
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Oak wilt disease may reduce the initial decay rate of dead Quercus serrata stems by altering wood-inhabiting fungal communities
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Methodology matters for comparing coarse wood and bark decay rates across tree species
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Rates of Mass Loss During Root Decay on Hog Island, VA 1991-1993
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Data from: Exclusion of invertebrates influences saprotrophic fungal community and wood decay rate in an experimental field study
1. Decomposer communities perform an essential ecosystem function by recycling nutrients. However, the effect of higher trophic levels on microbial decomposer communities and rate of decomposition is poorly understood. We therefore conducted an exclusion experiment to test the effect of invertebrates on fungal decomposer communities in dead wood, repeated at 30 sites in two landscapes, and measured wood density to assess effect on decay rate. 2. Invertebrates were excluded from recently cut logs by cages with a 1 mm mesh net, and fungal communities in caged logs were compared to logs accessible to invertebrates by DNA metabarcoding analyses. Accessible logs included control logs, cage control logs and positive control logs. 3. We found that exclusion of invertebrates had a significant effect on fungal community composition. For example, the wood decay fungi Trametes versicolor and T. ochracea were significantly more abundant in accessible logs than in caged logs. The strongest effect on fungal community composition, however, was attributed to differing baseline conditions in the individual trees. When accounting for these baseline differences, caged logs had significantly higher wood density than control logs after two years, indicating lower rates of wood decay in caged logs. 4. Further studies, spanning several years, are required to fully understand the influence of invertebrates on fungi and wood decay. However, our results indicate that invertebrates influence both the composition of saprotrophic communities in dead wood and their decomposition function, which is vital to forest ecosystems.
Quantitative prediction of excited-state decay rates for radical anion photocatalysts
<p>The input and output files related to the DFT calculations carried out for the work entitled "Quantitative prediction of excited-state decay rates for radical anion photocatalysts" are loaded in this repository.</p> <p>The zip file contains the optimized geometries of the compounds involved in the job.</p> <pre> </pre>
Study of Viral Load Decay Rates in HIV Infected Participants Starting Treatment With Raltegravir (RAL) and Emtricitabine/Tenofovir Disoproxil Fumarate (TDF)
ClinicalTrials.gov study NCT00660972. IPD Sharing: Not stated. Countries: 1. Publications: 4.
Data from: Exclusion of invertebrates influences saprotrophic fungal community and wood decay rate in an experimental field study
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Data from: Detection and decay rates of prey and prey symbionts in the gut of a predator through metagenomics
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Data from: Initial colonization, community assembly, and ecosystem function: fungal colonist traits and litter biochemistry mediate decay rate
Priority effects are an important ecological force shaping biotic communities and ecosystem processes, in which the establishment of early colonists alters the colonization success of later-arriving organisms via competitive exclusion and habitat modification. However, we do not understand which biotic and abiotic conditions lead to strong priority effects and lasting historical contingencies. Using saprotrophic fungi in a model leaf decomposition system, we investigated whether compositional and functional consequences of initial colonization were dependent on initial colonizer traits, resource availability or a combination thereof. To test these ideas, we factorially manipulated leaf litter biochemistry and initial fungal colonist identity, quantifying subsequent community composition, using neutral genetic markers, and community functional characteristics, including enzyme potential and leaf decay rates. During the first 3 months, initial colonist respiration rate and physiological capacity to degrade plant detritus were significant determinants of fungal community composition and leaf decay, indicating that rapid growth and lignolytic potential of early colonists contributed to altered trajectories of community assembly. Further, initial colonization on oak leaves generated increasingly divergent trajectories of fungal community composition and enzyme potential, indicating stronger initial colonizer effects on energy-poor substrates. Together, these observations provide evidence that initial colonization effects, and subsequent consequences on litter decay, are dependent upon substrate biochemistry and physiological traits within a regional species pool. Because microbial decay of plant detritus is important to global C storage, our results demonstrate that understanding the mechanisms by which initial conditions alter priority effects during community assembly may be key to understanding the drivers of ecosystem-level processes.
Data from: A deteriorating state of affairs: how endogenous and exogenous factors determine plant decay rates
Woody plants store large quantities of carbon (C) and nutrients. As plants senesce and decay, these stores transfer to the soil or other organisms or are released to the atmosphere. Exogenous factors such as topographic position and microclimatic and edaphic conditions tied to locations affect decay rates; however, we know less about how exogenous relative to endogenous factors such as morphological, anatomical and chemical construction tied to plant species affect these rates, especially across different tissue types. We monitored stem, fine branch and leaf decay over 1 year in 'rot plots' distributed across four watersheds in ridge top and valley bottom habitats in a temperate deciduous oak-hickory forest at Tyson Research Center, MO, USA, in the Ozark Highlands for 21 species of woody plants that vary in their constructions. We found poor coordination across tissues in construction and decay, which likely reflects how functional constraints on living tissues influence recalcitrance to decay. Additionally, for all three tissues, species membership and construction were better predictors of decay than was location. Of the construction traits, chemical composition including total fibre, lignin, cellulose, hemicellulose and concentrations of multiple microelements were the best predictors of decay, although the strength of these relationships differed among tissues. Synthesis. We have long known that rates of biogeochemical cycling are influenced by exogenous factors, such as climatic and edaphic factors. Here, we show across plant tissues that endogenous factors, including species identity and tissue construction, can have stronger controls on rates of decay within our study system than do exogenous factors. However, it is likely that the relative strengths of these different controls change through time and among tissues. We predict that anatomical and morphological controls may be more important at early stages and exogenous factors may be more important at later stages of decay.
Data from: Accumulation rates and sources of external nitrogen in decaying wood in a Norway spruce dominated forest
Microbial respiration in dead wood contributes substantially to the long-lived forest carbon (C) pool and has a significant role in the forest nitrogen (N) cycle. Wood N content has been found to increase during the decay process; however, temporal dynamics and the sources of this external N remain unclear. To examine N dynamics at various stages of decomposition, we combined high variety of analytical methods on Norway spruce logs, including wood δ15N, N%, 14C-dating, fungal composition and N2 fixation rate. For N2 fixation rate, we also determined its dependency on ambient temperature and decay class, when estimating annual N2 fixation rates for our study site. N2 fixation was observed to have a major role in increasing wood N content during decay. For the most decayed wood, it accounted for 60% of the total N accumulation. Compared to other reports, where the annual temperature was similar to our site, the calculated annual fixation rate of 85 g N ha−1 year−1 is a low estimate. However, previous studies have not taken appropriately into account the dependency of N2 fixation rate on ambient temperature and decay class. Our δ15N model describing the sources of external N, statistical analysis and the fungal DNA composition of decayed wood suggest that other sources of external N accumulating in wood were soil-foraging wood-decay fungi and mycorrhizal fungi. Our study improves knowledge of the temporal dynamics of N accumulation in wood with advancing wood decay, the potential sources of external N and their relative significance. All of these factors are important for nitrogen as well as carbon models dealing with ecosystem responses to climate change.
Data from: Accumulation rates and sources of external nitrogen in decaying wood in a Norway spruce dominated forest
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Data from: Decay rates of leaf litters from arbuscular mycorrhizal trees are more sensitive to soil effects than litters from ectomycorrhizal trees
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