Lisa M. Ganio
Oregon State University
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Publication
Featured researches published by Lisa M. Ganio.
Frontiers in Ecology and the Environment | 2005
Lisa M. Ganio; Christian E. Torgersen; Robert E. Gresswell
The shape and configuration of branched networks influence ecological patterns and processes. Recent investigations of network influences in riverine ecology stress the need to quantify spatial structure not only in a two-dimensional plane, but also in networks. An initial step in understanding data from stream networks is discerning non-random patterns along the network. On the other hand, data collected in the network may be spatially autocorrelated and thus not suitable for traditional statistical analyses. Here we provide a method that uses commercially available software to construct an empirical variogram to describe spatial pattern in the relative abundance of coastal cutthroat trout in headwater stream networks. We describe the mathematical and practical considerations involved in calculating a variogram using a non-Euclidean distance metric to incorporate the network pathway structure in the analysis of spatial variability, and use a non-parametric technique to ascertain if the pattern in the emp...
Soil Biology & Biochemistry | 2002
Christopher W. Swanston; Bruce A. Caldwell; Peter S. Homann; Lisa M. Ganio; Phillip Sollins
Abstract Density fractions in soils differ in their turnover rates, but direct measurement of the C dynamics in the individual density fractions is limited. In 300-day incubations of mineral soils from forests in Washington and Oregon, USA, light fractions (LF), heavy fractions (HF), whole soils (WS), and physically recombined light and heavy fractions (RF), were measured for respiration and shifts in microbial biomass. A combined fraction was calculated from the incubation results of the light and heavy fractions, and called the summed fraction (SF). Carbon concentration followed the pattern: LF>RF>HF. In accordance with this pattern, when cumulative respiration was considered per gram of substrate, the physical fractions exhibited a predictable response: LF>RF>HF. However, when expressed per gram of initial C, the respiration of the LF was not significantly different from that of the HF. These findings suggest the recalcitrance of HF is similar to that of LF and, consequently, differences in their turnover rates in WS may be due to microbial accessibility or physical protection. Whether expressed per gram of substrate or per gram of initial C, the respiration of the SF was not different from that of the WS. Within the SF, the HF was responsible for 35% of the total respiration. Lower respiration in the RF compared with WS and SF might be explained by an antagonistic interaction between the varied microbial communities that degrade LF and HF; in the heterogeneous WS, these communities may be spatially separated to a greater extent than in the laboratory substrate. Unfortunately, the microbial data were highly variable and provided little evidence to either support or refute this idea. The density separation technique appears to be a viable method for isolating different soil organic matter fractions. However, the function of these fractions should be considered more carefully in the context of accessibility and C content.
Plant and Soil | 1997
Paul T. Rygiewicz; Mark G. Johnson; Lisa M. Ganio; David T. Tingey; Marjorie J. Storm
Climate change (elevated atmospheric CO2, and altered air temperatures, precipitation amounts and seasonal patterns) may affect ecosystem processes by altering carbon allocation in plants, and carbon flux from plants to soil. Mycorrhizal fungi, as carbon sinks, are among the first soil biota to receive carbon from plants, and thereby influence carbon release from plants to soil. One step in this carbon release is via fine root and mycorrhizal turnover. It is necessary to know the lifetime and temporal occurrence of roots and mycorrhizae to determine the capacity of the soil ecosystem to sequester carbon assimilated aboveground. In this study, ponderosa pine (Pinus ponderosa Laws) seedlings were grown under three levels of atmospheric CO2 (ambient, 525 and 700 μmol CO2 mol-1) and three levels of annual nitrogen additions (0,100 and 200 kg N ha-1) in open-top chambers. At a two-month frequency during 18 months, we observed ectomycorrhizal root tips observed using minirhizotron tubes and camera. The numbers of new mycorrhizal root tips, the numbers of tips that disappeared between two consecutive recording events, and the standing crop of tips at each event were determined. There were more mycorrhizal tips of all three types seen during the summer compared with other times of the year. When only the standing crop of mycorrhizal tips was considered, effects of the CO2 and N addition treatments on carbon allocation to mycorrhizal tips was weakly evident. However, when the three types of tips were considered collectively, tips numbers flux of carbon through mycorrhizae was greatest in the: (1) high CO2 treatment compared with the other CO2 treatments, and (2) intermediate N addition treatment compared with the other N addition treatments. A survival analysis on the entire 18 month cohort of tips was done to calculate the median lifetime of the mycorrhizal root tips. Average median lifetime of the mycorrhizal tips was 139 days and was not affected by nitrogen and CO2 treatments.
Biogeochemistry | 2004
Christopher W. Swanston; Peter S. Homann; Bruce A. Caldwell; David D. Myrold; Lisa M. Ganio; Phillip Sollins
Nitrogen addition may alter the decomposition rate for different organic-matter pools in contrasting ways. Using a paired-plot design, we sought to determine the effects of long-term elevated N on the stability of five organic-matter pools: organic horizons (Oe+a), whole mineral soil (WS), mineral soil fractions including the light fraction (LF), heavy fraction (HF), and a physically recombined fraction (RF). These substrates were incubated for 300 days, and respiration, mineralized N, and active microbial biomass were measured. Samples with elevated N gave 15% lower cumulative respiration for all five substrates. Over the 300-day incubation, the Oe+a gave twice the cumulative respiration (g C kg−1 initial C) as the LF, which gave slightly higher respiration than the HF. Respiration was 35% higher for the WS than for the RF. Mineralized N was similar between N treatments and between the LF and HF. Net N mineralized by the LF over the course of the 300-day incubation decreased with higher C:N ratio, due presumably to N immobilization to meet metabolic demands. The pattern was opposite for HF, however, which could be explained by a release of N in excess of metabolic demands due to recalcitrance of the HF organic matter. Mineralized N increased with respiration for the HF but showed no pattern, or perhaps even decreased, for the LF. WS and RF showed decreasing active microbial biomass near the end of the incubation, which corresponded with decreasing respiration and increasing nitrate. Our results show that long-term elevated N stabilized organic matter in whole soil and soil fractions.
Forest Ecology and Management | 1998
Steven A. Acker; T.E. Sabin; Lisa M. Ganio; W.A. McKee
Abstract Interest in the contributions to biological diversity of old-growth forests has increased in many regions of the world. In the Pacific Northwest of the United States, concern for the contributions has lead to proposals to extend the rotation between timber harvests from the conventional 40–80 years to 150 years and longer. However, the implications of such a change for both development of old-growth structure and timber production are unknown. We examined long-term records (up to 82 years) from permanent plots established in 20 stands of Pseudotsuga menziesii (Mirb.) Franco in western Oregon and Washington that are approaching these proposed rotation ages. Similarity to old-growth structure was assessed by comparing the observed values of four structural variables to published mean values for young and old-growth forest. The assessment of similarity to old-growth structure was limited to characteristics of the live forest stand, due to the lack of measurements of snags and downed logs at initiation of the permanent plots. Timber production was assessed by examining trends in mean annual increment (MAI) of cubic volume. Development towards old-growth structure was rapid up to about age 80 years, and gradual thereafter. About half of the transition from young to old-growth forest structure occurred by age 100 years. Stands least similar to old-growth in early observations had relatively high tree densities and relatively small trees of uniform size. In later observations, stands most similar to old-growth structure were those with higher densities of large (>100 cm DBH) P. menziesii . In general, MAI declined gradually, averaging about 0.3% per year. Thus, longer rotations may not result in large declines of timber growth while providing for forest structure similar to old-growth. Early control of tree density may serve to hasten development of old-growth structure. Our approach to understanding the development of old-growth forest structure could be applied to long-term plot data from forests in other regions, as long as there is adequate information on old-growth and other forest stages.
Journal of Herpetology | 1998
Torrey Tyler; William J. Liss; Robert L. Hoffman; Lisa M. Ganio
Introduced fish have been implicated as reducing abundance or eliminating ambystomatid salamanders from montane lakes in wester North America. We tested the null hypotheses that survivorship, growth, and refuge use of larvae reared for 30 d did not differ between artificial ponds with trout and without trout Larval survivorship for both A. macrodactylum and A. gracile was significantly lower in ponds with trout than in fishless ponds. Both species had significantly lower snout-vent lengths in ponds with trout than in fishless ponds at the conclusion of the experiments. Only A. gracile had significantly lower body weight in ponds with trout than in ponds without trout For both species, substrate locations of larvae were significantly influenced by trout at the conclusion of the experiments. Larvae of both species were found in a narrower range of substrates in ponds with fish than in control ponds. Our findings support inferences from field studies that the presence of trout have negative impacts on larval A. macrodactylum and A. gracile.
International Journal of Wildland Fire | 2012
Travis Woolley; David C. Shaw; Lisa M. Ganio; Stephen A. Fitzgerald
Logistic regression models used to predict tree mortality are critical to post-fire management, planning prescribed burns and understanding disturbance ecology. We review literature concerning post-fire mortality prediction using logistic regression models for coniferous tree species in the western USA. We include synthesis and review of: methods to develop, evaluate and interpret logistic regression models; explanatory variables in logistic regression models; factors influencing scope of inference and model limitations; model validation; and management applications. Logistic regression is currently the most widely used and available technique for predicting post-fire tree mortality. Over 100 logistic regression models have been developed to predict post-fire tree mortality for 19 coniferous species following wild and prescribed fires. The most widely used explanatory variables in post-fire tree mortality logistic regression models have been measurements of crown (e.g. crown scorch) and stem (e.g. bole char) injury. Prediction of post-fire tree mortality improves when crown and stem variables are used collectively. Logistic regression models that predict post-fire tree mortality are the basis of simple field tools and contribute to larger fire-effects models. Future post-fire tree mortality prediction models should include consistent definition of model variables, model validation and direct incorporation of physiological responses that link to process modelling efforts.
Marine Pollution Bulletin | 1996
Christine A. Ribic; Lisa M. Ganio
In the US, a monitoring programme is being planned to evaluate national trends in beach litter. Power analysis was used to determine if the programme had a high probability of detecting a specified effect. We compared the use of a repeated measures model and a one-way analysis of variance model to investigate the power of detecting a 20% linear decrease in litter on beaches over a 5-year period, with power of 0.84 or more, a Type I error rate of 0.05, and quarterly sampling. We used the average coefficient of variation and, for the repeated measures model, average autocorrelations as estimates of model parameters. Common debris items typically had positive autocorrelations and use of the repeated measures model produced sample size estimates smaller than those from the analysis of variance model. Sample size estimates critically depend on reliable estimates of the mean, variance, and covariance of debris items of interest.
Trees-structure and Function | 2006
Sonya M. Dunham; Lisa M. Ganio
We used a Bayesian hierarchical model to analyze the variation in xylem anatomy, hydraulic properties, and the relationship between anatomy and properties within Douglas-fir trees. The hierarchical scales in our study included fertilization treatments (fertilized and unfertilized), trees within the treatments, and positions within the trees. We measured tracheid diameter, tracheid length, percent latewood, number of pits per cell, density, and specific conductivity (Ks) on seven positions in each of 16 fertilized and 16 unfertilized trees: the trunk at cambial age 52 (breast height), 25, and 5; a branch at cambial age 20 and 7; and a root at cambial age 42 and 22. Vulnerability to embolism was also measured on the oldest trunk, branch, and root positions. For any measurement, there was little variation between treatments, however, there was great variation among positions. Tracheid diameter, tracheid length, number of pits per cell, Ks, and vulnerability to embolism decreased vertically from the roots to the branches. Correlations were evident between some positions for tracheid diameter, percent earlywood, pits per cell, and vulnerability to embolism, mostly in the fertilized treatment. We found evidence for large-scale relationships (among all observations from all trees) between density and tracheid diameter, Ks and diameter, vulnerability and diameter, Ks and pits per cell, and vulnerability and pits per cell. At a smaller scale of within position, however, usually only the branches and roots maintained the relationship.
Transactions of The American Fisheries Society | 2014
R. Flitcroft; Kelly M. Burnett; J. Snyder; Gordon H. Reeves; Lisa M. Ganio
AbstractPatterns of salmon distribution throughout a riverscape may be expected to change over time in response to environmental conditions and population sizes. Changing patterns of use, including identification of consistently occupied locations, are informative for conservation and recovery planning. We explored interannual patterns of distribution by juvenile Coho Salmon Oncorhynchus kisutch in 11 subbasins on the midcoast of Oregon. We found that juvenile Coho Salmon distribution expanded and contracted around stream sections that were continuously occupied (core areas). Timing of expansion or contraction was synchronous among subbasins and appeared to be related to the size of the parental spawning run. Juvenile distribution expanded from core areas when adults were abundant and contracted into core areas at lower adult abundances. The “intrinsic potential” of stream sections to support high quality habitat for Coho Salmon also appeared to inform distribution patterns. In most subbasins, when popula...