Methods:
Study site and experimental design: My field research will take place from June 14th to August 8st, 2021 in the Forest Resilience and Threshold Experiment (FoRTE) plots situated on University of Michigan Biological Station Property. The FoRTE study design contains 4 replicate plots distributed across a 16ha area. Each replicate represents a disturbance severity gradient containing four 0.5ha plots randomly assigned to a treatment of either 0% (control), 45%, 65% or 85% tree biomass mortality. Each 0.5 ha plot is divided in half, creating two subplots that will be designated as either “top-down” or “bottom-up”, representing two different disturbance types. Within each of the 32 subplots, there are 5 evenly spaced collection sites where bulk soil respiration collars, root in-growth cores and leaf litter traps are spatially paired. In addition, there are four 1m2 destructive soil plots in each subplot where soil samples will be collected for in vitro heterotrophic respiration.
Bulk soil respiration (Rs): To continue assessing soil carbon stability across a disturbance severity gradient, Rs will be measured concurrently with soil temperature (Ts) and soil moisture (2). Rs will be measured with a Licor-6400 portable gas analyzer and closed soil CO2 chamber (LI-COR Inc, Lincoln, NE, USA), Ts will be measured to 7cm with a thermal couple wire attached to the LI-COR and 2 will be measured to 20cm with a CS620 soil moisture probe. Rs measurements will be taken at all 160 soil collars twice a month for a total of 6 measurements per collar.
Heterotrophic respiration (Rh): To isolate the microbial component of Rs across a disturbance severity gradient, Rh will be measured using an in-vitro root-free soil incubation technique. 3 pseudo-replicate soil cores will be harvested to 10 cm in all 132 destructive soil plots. Soil cores will be stored for 24 hours at 4C before being processed and sieved to eliminate roots. Root-free soil will be weighed into ventilated mason jars and incubated at the average soil temperature (Ts ) for two weeks and then Rh will be measured with a LI-6400 and custom soil chamber cuvette (Curtis et al 2005). Four efflux values will be recorded in each mason jar over 90 second intervals. Soil jars will be vented for 75 mins to stabilize gas exchange before measuring (time to stabilization was determined from a degassing trial with a randomized subset of soil jars, n = 5). Rh will be measured from all 132 destructive soil plots once a month for a total of 3 samples per plot.
Fine-root production: To measure changes in fine-root NPP across a disturbance severity gradient, 20cm mesh in-growth cores were paired with each Rs collar. 4 cores will be re-installed in each subplot for a total of 120 cores. Cores will be kept in the soil for the remainder of the growing season and harvested in November 2021. Total root NPP will be estimated by scaling dried fine-root mass from each in-growth core.
Fine-root structure: To measure rhizosphere structural changes across a disturbance severity gradient, changes in specific root length and diameter will be quantified by collecting fine-root samples from all 132 destructive soil plots. Samples will be analyzed using the WinRhizo scanner and software package. To quantify compensatory root growth post disturbance, WinRhizo will be used to identify individual roots by species.
Funding agency:
National Science Foundation