Abstract
Global climate change models indicate that storm magnitudes will increase in many areas throughout southwest North America, which could result in up to a 25% increase in seasonal precipitation in the Big Bend region of the Chihuahuan Desert over the next 50 years. Seasonal precipitation is a key limiting factor regulating primary productivity, soil microbial activity, and ecosystem dynamics in arid and semiarid regions. As decomposers, soil microbial communities mediate critical ecosystem processes that ultimately affect the success of all trophic levels, and the activity of these microbial communities is primarily regulated by moisture availability. This research is focused on elucidating soil microbial responses to seasonal and yearly changes in soil moisture, temperature, and selected soil nutrient and edaphic properties in a Sotol Grassland in the Chihuahuan Desert at Big Bend National Park. Soil samples were collected over a 3-year period in March and September (2004–2006) at 0–15 cm soil depth from 12 3 × 3 m community plots. Bacterial and fungal carbon usage (quantified using Biolog 96-well micro-plates) was related to soil moisture patterns (ranging between 3.0 and 14%). In addition to soil moisture, the seasonal and yearly variability of soil bacterial activity was most closely associated with levels of soil organic matter, extractable NH4–N, and soil pH. Variability in fungal activity was related to soil temperatures ranging between 13 and 26 °C. These findings indicate that changes in soil moisture, coupled with soil temperatures and resource availability, drive the functioning of soil-microbial dynamics in these desert grasslands. Temporal patterns in microbial activity may reflect the differences in the ability of bacteria and fungi to respond to seasonal patterns of moisture and temperature. Bacteria were more able to respond to moisture pulses regardless of temperature, while fungi only responded to moisture pulses during cooler seasons with the exception of substantial increased magnitudes in precipitation occurring during warmer months. Changes in the timing and magnitude of precipitation will alter the proportional contribution of bacteria and fungi to decomposition and nitrogen mineralization in this desert grassland.
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Introduction
Precipitation pulse sizes and corresponding soil moisture in arid ecosystems are discrete and highly variable events [1]. These discontinuous moisture pulses provide a window of opportunity for soil microbes, triggering mineralization for brief periods, and consequently releasing nitrogen and other minerals into the upper soil horizons [2–4]. However, primary producers in arid systems rarely benefit from brief moisture pulses, as plant growth is dependent not only on soil microbial activity, but also on other factors including the duration of the precipitation event, amount of soil water infiltration and subsequent soil moisture levels, and plant functional types [5, 6]. Consequently, short-term increases in soil microbial activity triggered by moisture pulses in arid systems will not typically correspond to subsequent increases in primary production on the same time scale. As decomposition and consequent mineralization can be stimulated by moisture pulses that are too brief to benefit primary producers [2, 7, 8], there is potential for soil nutrient pools to accumulate over time in desert soils and then become available to plants as heavier precipitation events occur. In addition, any accumulation of soil nutrients as a consequence of mineralization pulses caused by brief soil moisture pulses may subsequently influence microbial functional dynamics and consequently alter soil microbial community diversity.
Increased root and soil microbial respiration rates in response to isolated moisture pulses has been shown to occur in the Sonoran Desert at both Saguaro National Park and the Santa Rita experimental range outside Tucson, AZ, and in the northern Chihuahuan Desert at the Sevilleta National Wildlife Refuge in central New Mexico [9–11]. However, current understanding is incomplete as to how belowground microfloral dynamics in deserts functionally respond to environmental variation over a several-year period and how environmental variation might influence soil microbial biodiversity across arid landscapes [12–15]. Even less is known about how changes in soil microbial biodiversity will influence processes such as decomposition and mineralization rates in arid systems, and how ecosystem function will subsequently be affected as climate change results in altered precipitation patterns [15–20]. These questions are important to answer because available soil moisture is predicted to become increasingly variable in arid systems as a consequence of global climate change. Moreover, changes in plant productivity, root growth, and exudation patterns as a consequence of climate modifications are likely to significantly influence microbial diversity and activity [21–23]. These impacts will most likely occur through changes in soil organic matter levels, decomposition, and mineralization rates [24–29]. Thus, by evaluating microbial functional responses to current environmental patterns, potential impacts of climate change on soil microbial function can be addressed.
Assessment of carbon utilization patterns of soil microbial communities, as affected by soil moisture or temperature patterns, can provide some insights into microbial functional responses to environmental changes in arid regions. The Biolog procedure was introduced initially to identify bacterial functional differences between soil and water samples [30]. Zak et al. [31] used this procedure to measure soil bacterial functional diversity along a moisture gradient in the Chihuahuan Desert at the Jornada Long-Term Ecological Research site and reported considerable variation in the ability of bacterial communities to utilize different carbon substrates along the gradient. Zak et al. [32] later used this approach to examine bacterial carbon use along an extensive elevation gradient in the Chihuahuan Desert at Big Bend National Park. Using similar methodology, the FungiLog approach was then developed [33, 34] to determine saprophytic fungal functional diversity associated with decomposed plant material and soil. Although the Biolog method is limited, as results cannot reflect accurately the carbon use potential of the bacterial community as a whole, the capacity of this approach for estimating microbial response patterns to various treatments, disturbance, or environmental conditions has been recognized [35, 36]. Employing these two methods, potential carbon usage of both saprophytic fungi and soil bacteria in response to temporal patterns of moisture and temperature in arid systems can be ascertained. Linking bacterial and saprophytic fungal carbon use to changes in soil moisture patterns, nitrogen availability, or soil temperature will be crucial for understanding consequences of changes in precipitation patterns on soil microbial dynamics in arid landscapes.
The objective of this research was to determine patterns of soil microbial and soil nutrient dynamics in a Chihuahuan Desert grassland at Big Bend National Park in response to temporal differences in environmental conditions with the goal of providing insight as to how global climate change predictions for this region will subsequently influence soil microbial activity and function and ultimately ecosystem process.
Materials and Methods
Site Description
This research was conducted in a Sotol Grassland site in the Pine Canyon Watershed [32], located in Big Bend National Park (BBNP), Texas. BBNP is located in the central region of the Chihuahuan Desert and is characteristic of the Chihuahuan Desert because of its many mountain ranges and diverse plant communities [37, 38]. Like the Chihuahuan Desert (taken as a whole), BBNP receives the majority of its rainfall in the summer months from moisture brought in by southeasterly winds blowing over from the Gulf of Mexico, with the least amount of precipitation occurring during winter months [39, 40]. Precipitation data collected at Big Bend’s Panther Junction Visitor Center over the past 19 years shows the average winter rainfall (December–February) to be 55.9 mm, whereas the average summer rainfall (June–August) is 163.3 mm. The average total annual rainfall for BBNP over the past 19 years is 364 mm. Average daily air temperatures in BBNP range from ~10 °C in the winter months to ~32 °C in the summer (Fig. 1).
The research site for this study is located in the Sotol Grasslands in the Pine Canyon Watershed, which is situated on the northeast side of the Chisos Mountains (centrally located in BBNP). This desert grassland site is higher in elevation (1500–1678 m) than other components of the Chihuahuan Desert; consequently, climate is slightly wetter and cooler than for lower elevation grasslands in the Chihuahuan Desert. Dominant plants include sotol (Dasylirion leiophyllium), several species of prickly pear (Opuntia phaeacantha, Opuntia engelmannii, Opuntia violacea, and Opuntia rufida) and grama grasses (Bouteloua capitola, Bouteloua curtipendula, and Bouteloua hirsute). In general, desert grasslands are characterized as having the lowest biomass levels of any North American grassland type [41].
The Pine Canyon Sotol Grassland is located in a caldera (latitude: 29°5.86″ N; longitude: 103°14′13.54″ W), and the magma produced from the area is the major source forming the surrounding Chisos Mountains [42]. Soils in Pine Canyon typically have an extremely rock-strewn A-horizon with little to no litter layer that immediately overlays a fractured igneous bedrock foundation. This soil is described as Lajitas-rock outcrop complex by USDA soil surveys [43, 44]. The soil texture throughout this site has been determined to be a sandy–loam (62% sand, 30% silt, 8% clay) by Waters Agricultural Laboratories, Inc. (Owensboro, KY).
Experimental Design
We established 12 3 × 3 m community plots to study long-term soil microbial and plant responses to seasonal patterns in precipitation. These community plots were constructed to uniformly encompass the three dominant plant species of the Sotol Grasslands in Pine Canyon (sotol, prickly pear, and grama grasses). Twenty-four soil samples (two per plot) were collected biannually in March and September for three consecutive years starting in 2004. These months were chosen to represent the ends of the winter and summer seasons at BBNP, which are the two seasons predicted to experience the greatest shift in precipitation patterns due to global climate change in this region [45, 46]. Soil was collected from 0 to 15 cm depths and stored at 4 °C until use. All soils were analyzed within 2 weeks of collection.
Assessing the Potential Carbon Usage of Soil Microbes
Microbial functional responses to environmental conditions were assessed by analyzing potential carbon usage for both bacteria and fungi. To quantify bacterial responses, soil samples were diluted to 10−4 and inoculated into Biolog GN2 96-well microtiter plates containing 95 different carbon substrates following the Biolog method [30, 31, 36, 47]. Fungal functional responses were assessed by inoculating Biolog SFN2 96-well microtiter plates containing 95 different carbon substrates with a 20 ml inoculation mixture containing 50 mg SOM particles (ranging between 250 and 500 μm) following Soil Fungilog procedures. Soil organic matter particles were separated from the mineral soil fraction using the procedure as outlined by Sobek and Zak [34]. Functional responses for bacteria and fungi were quantified for total substrate activity and substrate richness after 72- and 120-h incubation periods. The 72- and 120-h incubation periods were chosen to allow for the most complete expression of microbial carbon use potential at the time of sampling [31, 34, 48]. Substrate activity refers to the sum of combined ability to utilize the different carbon substrates, whereas substrate richness refers to the number of wells (95 total wells) that have any level of carbon-use activity.
Nitrogen Dynamics
Exchangeable soil ammonium (NH4–N) was determined via colorimetric assay and was extracted one day after the sample collection date using a 50-ml 2-M KCl solution from a 5-g field moist (oven dry equivalent) soil sample [49]. Levels of extractable NO3–N were determined 1 day after the sample collection date by A&L Soil Laboratories (Lubbock, TX, USA) using ion-specific probes.
Potential Nitrogen Mineralization
Soil incubations were employed to evaluate seasonal changes in potential nitrogen mineralization patterns as described by Robertson et al. [27]. Ninety-six 250 mL soil chambers were incubated after each sampling period beginning in 2006. Forty-eight chambers were used to incubate soil for 40 days, with the second set of 48 chambers incubated over 80 days. Soils throughout all incubation periods were kept at (24 °C). Initial watering application increased soil moisture to near saturation (~20% soil moisture). Soils slowly dried over the incubation intervals, and at the end of each incubation period, percent soil moisture was determined along with extractable soil NO3–N and NH4–N to assess net nitrogen mineralization rates, net nitrification rates, and relative percent nitrification [27]. Measurements of extractable NO3–N and NH4–N occurred as described above. Carbon to nitrogen ratios of initial, 40- and 80-day incubations were analyzed using a CE Elantech CHN analyzer (NCS 2500, Carlo Erba, Inc. Milan Italy) for samples collected in March and September 2006.
SOM
Soil organic matter (SOM) was estimated via loss-on-ignition method [50]. Soils were air-dried for 24 h, then placed in aluminum pans and oven-dried for an additional 24 h in a 60 °C drying oven. After drying for 24 h, approximately 10 g of soil was placed in a weighed porcelain crucible and then incinerated at 450 °C for 24 h. After incineration, samples were removed from the furnace and reweighed to determine ash weight remaining.
Microbial Biomass Carbon
Estimations of microbial biomass carbon (MBC) was accomplished using the chloroform fumigation and extraction method [51], in which two replicates from each soil sample were fumigated for 48 h, while another set of two replicates from each soil sample were not fumigated. Soil MBC was extracted using a 0.5-M K2SO4 solution from 5 g field moist (dry weight equivalent) soil sample and filtered using Fisherbrand-P2 fine-porosity filter paper. Extracted soil MBC was measured spectrophotometrically at 280 nm, and the difference between the extracted C in the fumigated and non-fumigated soils represents the microbial biomass C [52].
Environmental Parameters: Soil pH, Soil Moisture, and Air and Soil Temperatures
Soil pH was measured using a 2:1 paste extract [27]. Percent soil water content was measured at each sampling time by drying soils in a drying oven (60 °C for 48 h) [53]. Soil (15 cm depth) and air temperatures (1.0 m above soil surface) were collected using Onset Computer Corporation HOBO-H8 Pro Series data loggers at 36-min intervals [54]. For every sample period, average soil and air temperatures were calculated for 4 weeks before sampling occurred to represent environmental conditions critical for microbial response.
Statistical Analysis
The statistical approach used to assess significant differences in all observed parameters collected over the 3-year period (soil pH, soil organic matter percentage, microbial biomass, available soil NH4–N and NO3–N, in vitro mineralized soil NH4–N and NO3–N, soil C:N, net nitrification, net mineralization, relative percent nitrification, and potential carbon usage for both bacterial and fungal communities) was repeated-measures analysis of variance (rmANOVA) using the consecutive sample dates as the within subject variable using the statistical software package SPSS 14.0 (Chicago, Il, USA). To determine microbial and soil nutrient responses to environmental conditions, stepwise multiple regression analysis was performed (SPSS 14.0, Chicago, Il, USA; [55]). The stepwise method was chosen because this technique provides, as the first step, a single-variable model that accounts for the most variation and then calculates successively more complex models. This approach allows for an examination of the relative contributions of each variable to the most parsimonious descriptive model. Biolog, Fungilog, and available soil NH4–N and NO3–N data was modeled as a function of environmental parameters to assess microbial response and available nutrient relationships to environmental and edaphic variables (Table 1). Levels of extractable NO3–N and NH4–N from in vitro incubations were modeled as a function of percent soil moisture and the inorganic nitrogen counterpart recorded at the end of the incubations using multiple regression analysis to detect any relationships between soil nitrogen levels and soil moisture (Table 2). Every R 2 statistic reported in this experiment is from the final significant model (P ≤ 0.01) provided by the stepwise process. The stepping-method criteria entered any variable with the probability of F ≤ 0.005 and removed any variable from the model F > 0.01. Pearson correlations (Tables 1 and 2) were examined to identify any highly correlated variables that might corrupt the models generated by the multiple regression analysis. Only two variables, soil and air temperature, were found to be highly correlated (R > 0.80). Statistical analyses were conducted with SPSS 14.0 (Chicago, Il, USA). The sample size for regression analysis for bacterial and fungal responses and initial (in situ) extractable soil nitrogen levels collected over the 3-year study (between 2004 and 2006) is 144. The sample size for regression analysis for in vitro nitrogen mineralization data collected from soil incubation methods was from March and September 2006 only; the sample size for these data is 192.
Results
Environmental Parameters
Over the 3-year period, average soil temperatures within each sample period closely matched average air temperatures during the same sampling period and were highly correlated throughout the study (R = 0.98) (Fig. 2; Table 1). Soil and air temperatures in March were consistently lower than air and soil temperatures in September, with March temperature averages ranging from ~13–18 °C for soil and ~13–16 °C for air. In September, temperature averages ranged ~24–26 °C for soil and ~23–26 °C for air. Monthly precipitation varied throughout the 3-year period, with 2004 receiving above average annual rainfall (567 mm), 2005 receiving average rainfall (329 mm), and 2006 receiving below average rainfall (273 mm; Fig. 2a). Soil moisture throughout the 3-year study was observed to be highly variable and contingent on the timing and magnitude of moisture, ranging between 3.0 and 12.0% (VWC). The first three sample periods (March 2004, September 2004, and March 2005) exhibited soil moisture values typical for these desert grasslands (6–8%; Fig. 2b). For the duration of the next two sampling periods (September 2005 through March 2006), this region experienced an extended drought; consequently, very low soil moisture levels (<4.0%) were recorded. The highest soil moisture (11.98%) was recorded in the final sample period of September 2006 as a consequence of heavy rainfall (>140 mm) received during the month before this sampling period (Fig. 2b).
Soil pH
Soil pH maintained relatively consistent acidic conditions (pH 5.9–6.2) throughout the study. Soils collected during the last year of the study appeared slightly less acidic than the previous 2 years; however, only September 2004 displayed significantly higher acidity levels (P ≤ 0.031) than the last year of sampling (Fig. 3a).
SOM
Soil organic matter content tended to increase in March and decrease in September. However, this pattern was only significant in the first year (P < 0.001), whereas soil organic matter content over the last four sample periods, although exhibiting the same seasonal pattern observed in 2004, were not statistically significant (Fig. 3b).
Microbial Biomass Carbon
Microbial biomass carbon was relatively stable across season for the first 2 years of the study period, although MBC variability increased over time as annual precipitation decreased (Fig. 3c). MBC ranged from 218 μg g−1 in March 2004 to 335 μg g−1 in March 2006 to the highest amount (770 μg g−1) recorded in September 2006. MBC levels recorded in September 2006 were significantly higher (P ≤ 0.003) than MBC levels from all prior sample periods.
Nitrogen Dynamics
Extractable soil NH4–N at the time of sampling ranged from 2.44 to 20.09 mg kg−1, depending upon the sample period (Fig. 4a). The highest values were recorded during the last sample period in September 2006 when the highest percent soil moisture was recorded after an extended drought, and 2006 exhibited significantly higher levels of soil NH4–N than the first 2 years (P ≤ 0.046). Extractable soil NO3–N at the time of sampling fluctuated temporally with higher values recorded in September compared to March. Although these seasonal differences between March and September were observable throughout the study, this pattern was only significant (P ≤ 0.024) over the last 2 years (Fig. 4b).
In determining soil NO3–N dynamics in response to environmental conditions, air temperature (12–27 °C) was the sole predictor for seasonal and annual variability (R 2 = 0.31; Table 3). For NH4–N, a two-variable model was produced that included soil temperatures (13–27 °C) along with soil moisture as the two major determinants of seasonal and yearly variability (R 2 = 0.234; Table 3).
Nitrogen Mineralization
Soils collected in March and September 2006 displayed similar patterns with regard to how forms of inorganic nitrogen changed over time. Repeated measures ANOVA reported that in both sample periods, soil NH4–N levels significantly decreased between the initial and 40-day incubation period (P < 0.001; Fig. 5a–b). Levels of soil NH4–N remained constant between 40- and 80-day incubations in March 2006 (P = 0.068; Fig. 5a). In September 2006, NH4–N levels significantly increased (although slight) between the 40- and 80-day incubation period (P < 0.001; Fig. 5b). Initial NH4–N levels were relatively consistent over all incubations in both March and September 2006, as initial levels (~18.23 mg kg−1) were not significantly different from one another (P = 0.111; Fig. 5a–b). However, NH4–N levels after the 40- and 80 – day incubations were significantly higher in March 2006 than in September 2006 (P ≤ 0.031). Contrastingly, extractable soil NO3–N levels over the duration of the incubation displayed dramatic and significant increases from initial levels in both March and September during the first 40 days of incubation (P < 0.001). Ultimately, September NO3–N levels were significantly higher by the end of the 80-day incubation period (P < 0.001) than in March. The level of NO3–N was significantly higher by the end of the 40-day incubation period in September 2006 when compared to the 40-day incubation period in March 2006 (P < 0.001). Extractable NO3–N levels peaked in September by the end of the 40-day incubation period and did not change significantly from the subsequent 80-day incubation. However, NO3–N levels in March experienced significant increases between the 40- and 80-day incubation period (P < 0.001; Fig. 5a–b), but were still lower than NO3–N levels after the 40- and 80-day September incubations. Both forms of inorganic nitrogen were strongly related to soil moisture along with the inorganic nitrogen counterpart, and both soil NO3–N and soil moisture accounted for much of the observed variation of extractable soil NH4–N in the lab incubations (R 2 = 0.482; Table 3). Likewise, both soil NH4–N and soil moisture accounted for the much of the observed seasonal variation of NO3–N in the lab incubations (R 2 = 0.531; Table 3).
C:N Ratios
Soils collected in March and September 2006 displayed slightly different patterns with regard to how C:N dynamics responded throughout the incubation periods (Fig 5c). In both sample periods, C:N ratios significantly decreased between the initial and 40-day incubation period (P ≤ 0.003). C:N ratios remained constant between 40- and 80-day incubations in March 2006 (P = 0.439), whereas C:N ratios between 40- and 80-day incubations in September 2006 continued to significantly decrease (P = 0.001).
Net Nitrification, Net mineralization, and Relative Percent Nitrification
There were no significant differences in the daily rates of net nitrification between 40- and 80-day incubation periods in March 2006 (Fig. 6). Significant changes in daily rates of net nitrification were observed between the 0- to 40-day and the 0- to 80-day incubations in September 2006 (Fig. 6), as net nitrification/day after the 40-day incubation measured 1.98 mg kg−1 day−1. By the end of the 80-day incubation period, these nitrification rates significantly dropped to 0.98 mg kg−1 day−1, (P < 0.001). Net nitrogen mineralization rates in March 2006 displayed similar patterns as net nitrification, as no significant increases occurred between the 40- and 80-day incubation periods. Likewise, September experienced significantly higher nitrogen mineralization rates than did March after the 40-day incubation period (P ≤ 0.001). However, net mineralization rates dropped significantly by the end of the 80-day incubation period in September (40-day 1.52 mg kg−1 day−1 to 80-day 0.75 mg kg−1 day−1) (P ≤ 0.001). Relative percent nitrification throughout the March 2006 (0–40 day) incubation period increased nitrogen levels in the soil by 167% (Fig. 7a); however, by the end of the 80-day incubation period, relative percent nitrification significantly dropped to 44% of the first 40 days (P < 0.001). Relative percent nitrification in September 2006 during the 0- to 40-day and 0- to 80-day incubations did not significantly differ (Fig. 7b), exhibiting an average of 133% for the two periods. When comparing the two incubation intervals independently (0–40 vs 40–80 days), significant declines of relative percent nitrification (P < 0.001) were observed during the 40- to 80-day incubation periods in both March and September from the first 0- to 40-day period to less than 100% (Fig. 7b).
Bacterial Carbon-Use Potential
Potential bacterial carbon usage, measured in terms of total substrate activity (BSA) and substrate richness (BSR), were variable across sample periods with the highest values recorded in September 2006 (Fig. 8, 9). Lower values for BSA and BSR were associated with periods of low soil moisture. Temporal patterns in potential carbon usage by bacteria in the micro-wells were similar across incubation times. Higher values were recorded after the 120-h incubation (Fig 9a–b). Soil moisture was the dominant single parameter accounting for the seasonal and yearly variability of BSA after 72-h incubation (R 2 = 0.313; P < 0.001; Table 4), whereas soil moisture, soil NH4–N, and soil pH were related to carbon use patterns after 120-h incubations (R 2 = 0.446; P < 0.001). Variation in BSR after the 72-hr incubation period was related to soil moisture and levels of soil NH4–N (R 2 = 0.463; P < 0.001) (Table 4). For BSR after 120-hr incubations, soil moisture, levels of soil NH4–N, soil organic matter, and soil pH levels accounted for the most variation (R 2 = 0.515; P < 0.001).
Fungal Carbon-Use Potential
Significant differences in total substrate activity (FSA) for the 72-h incubation periods were exhibited over all sample periods (P ≤ 0.03; Fig. 8a). Overall substrate diversity (FSR) was significantly different throughout most of the study (September 2004–March 2006; P ≤ 0.038; Fig. 8b); however, the first sample period in March 2004 and the last sample period in September 2006 were not significantly different from one another. Potential fungal carbon use followed temporal patterns of increased activity in March vs September coupled with annual precipitation levels; however, fungal activity dramatically increased in September 2006. Soil moisture and soil temperature accounted for most of the seasonal and yearly variability (R 2 = 0.388; P < 0.001) in fungal substrate activity (FSA) after 72-h incubations (Table 4). For FSR after the 72-h incubation period, soil moisture and soil temperature were also significant (R 2 = 0.342; P < 0.001; Fig. 8b; Table 4). Soil moisture was the only variable (R 2 = 0.118; P < 0.001) that accounted for temporal variability in fungal substrate activity after the 120-h incubation.
Discussion
Environmental Parameters
The Chihuahuan Desert is unique in that it is the only North American Desert that receives the majority of it’s annual precipitation exclusively in the summer months, with minor pulses contributing to annual net precipitation during the fall, winter, and spring months [38–40]. Annual precipitation and temperature patterns in the Sotol Grasslands in Pine Canyon at BBNP are relatively consistent with the Chihuahuan Desert as a whole. Over this 3-year study annual precipitation steadily declined, ranging from an unusually wet year in 2004 (567 mm; 155% of the 19-year average), to average precipitation levels received in 2005 (329 mm; 90% of 19-year average), to drought-like conditions in most of 2006 (273 mm; 74% of 19-year average). The timing and magnitude of intra-seasonal precipitation in the Chihuahuan Desert is highly dynamic and varies greatly from year to year, as seasonal soil moisture variability reflects the timing and magnitude of precipitation, number of dry days between rain events, soil temperatures, and evapotranspiration rates [4, 56, 57]. The 2006 sampling year is a good example of how variable this system can be between years as this region experienced an extreme drought that started in late Fall in 2005 and continued throughout the first half of 2006, in which only 79 mm occurred between Jan–July 2006 (39% of historical averages for this period). Intense rainfall events occurred throughout August 2006. The total rainfall recorded for this month was 147.4 mm, which is 90% of historical rainfall received for the entire summer season (June, July, and August), producing 54% of the precipitation received in 2006.
Understanding soil microbial responses to soil moisture and rainfall is crucial to determine ecosystem responses to climate change. Soil microbes are typically the first responders to soil moisture pulses in arid systems and soil microbial functional capabilities in arid systems are directly linked to precipitation and resource availability [5, 8, 58]. The severe drought event that began in late 2005 and continued through mid-summer of 2006 allowed us to observe how soil microbes will respond to occurrences of extended drought periods accompanied by brief but intense precipitation events. These climate events are important to document because extreme drought patterns accompanied by increased magnitudes of brief precipitation events are predicted to increase significantly throughout the 21st century in the arid regions of SW North America as reported by the Third Assessment Report of the Intergovernmental Panel on Climate Change (IPCC; [45]). The stability of this desert grassland ecosystem as climate change occurs is likely to rely on the ability of soil microbes to function during these brief moisture windows of opportunity [3]. The dynamics of how properties such as soil pH, levels of soil NO3–N and NH4–N, and amounts of soil organic matter respond to these windows of opportunity can also greatly influence soil microbial dynamics in this ecosystem [56, 59].
Soil Carbon and Nitrogen Dynamics
When considering that the majority of precipitation occurs throughout the summer months in this region, the overall observed pattern of soil organic matter dynamics is similar to previous studies in which soil moisture dynamics (drying–rewetting) promotes loss of soil organic matter as it becomes more readily used by microbes as the primary source of nitrogen (via mineralization; [59–61]).
The soil organic matter patterns observed in this study suggest that the magnitude and timing of intra-seasonal precipitation is a key regulator for microbial ability to utilize soil organic matter. Our observations support this because regardless of 2005 receiving 50 mm more precipitation than 2006 by the end of the summer season, more soil organic matter was depleted in 2006, in which a few intense rainfall events occurred in August as opposed to the more frequent, less intense events throughout 2005. This suggests that soil microbes in this desert grassland are resilient to extended drought and seasonal resource depletions and are able to quickly respond to increases in soil moisture pulses as they occur.
The nitrogen mineralization dynamics observed in this desert grassland further support these seasonal microbial activity patterns as nitrate levels were greater in September and lower in March, which inversely followed patterns in soil organic matter amounts. Moreover, levels of soil NO3–N were negatively correlated with soil organic matter (R = −0.208). Both relative nitrification and nitrate levels significantly increased with moisture pulses, while soil NH4–N levels declined, indicating that both soil moisture and temperature are key controlling factors regulating mineralization in this system [2, 60].
The in vitro potential N-mineralization patterns observed in this study were similar to results from previous semiarid grassland studies [2, 9], in which soil NH4–N levels at the time of collection were consistently higher than soil NO3–N levels at initial collection; while over time throughout the incubation periods, dramatic increases in NO3–N levels were observed (with added moisture), while NH4–N levels dropped dramatically over the same incubation period. Temporal differences in the rates of in vitro mineralization reflect the seasonal regulation of microbial metabolic potential, as both net nitrification and net mineralization rates in September far exceeded that of March. This indicates that above and beyond soil moisture, seasonal soil temperature is a second key regulating mechanism in this system influencing soil microbial functionality in this desert grassland by possibly down regulating soil microbial mineralization capabilities. Consequently, as seasonal temperatures increase as predicted by global climate-change models, changes in precipitation, temperature, and soil moisture dynamics has the potential to greatly shift the soil microbial metabolic potential in this desert grassland system, which could, in turn, potentially alter the functionality of this ecosystem.
Microbial Parameters
Patterns in microbial biomass were observed to correspond with peaks in soil moisture levels. The dramatic shift in microbial responses from extreme drought to above average soil moisture in September 2006 demonstrates the resilience of the soil microbes in this system to remain viable enough during periods of drought to quickly respond to moisture windows of opportunity as they occur. Furthermore, these responses reveal how temperature regulates seasonal MBC, as the MBC levels in March (promptly after the winter season) are unable to respond to soil moisture availability, but in September 2006, MBC does respond to moisture pulses regardless of prior temperature-stress conditions. Lower MBC levels recorded during the years with higher precipitation in 2004 and 2005 may suggest that microbial activity peaked earlier in the summer season with the earlier moisture pulses, thus depleting necessary resources. Another likely scenario is that microbial grazing by microfauna could be stimulated during the wetter years, which could reduce microbial biomass levels by the September sample collection period [62]. In addition, overall seasonal MBC levels in September were significantly higher than March, suggesting that soil temperatures could restrict microbial activity regardless of the availability of soil moisture and available soil nitrogen. Similar microbial biomass dynamics have been observed in previous studies in which increased soil microbial biomass carbon correlated with elevated soil moisture and nitrogen mineralization rates as available soil moisture was shown to stimulate microbial biomass turnover in arid systems [63–66]. Other studies conducted by Kieft et al. and Van Gestel [61, 67] argue that osmotic shock can occur from intense rewetting of dry soils, resulting in cell lyses, from which remaining soil microbes can utilize labile organic carbon and nitrogen occurring from turnover. However, it is unclear to what degree microbial osmotic shock associated with precipitation events are responsible for observed patterns in microbial biomass and potential carbon usage in the soils of the Sotol Grasslands at BBNP. Potential carbon utilization dynamics for both fungi and bacteria displayed patterns that corresponded to seasonal and yearly soil moisture patterns over time; however, the responses to precipitation contrasted between bacteria and fungi. Bacterial substrate activity and substrate richness declined over much of the study directly tracking the annual declines in precipitation and soil moisture. These patterns suggest that bacterial carbon use is directly regulated by precipitation and subsequent soil moisture dynamics in this desert grassland.
Fungal carbon-use responses exhibited significant seasonal shifts with elevated early spring activity. Fungal abilities to use carbon substrates in this system demonstrated much weaker correlations to soil moisture over the 3-year study than did bacteria, as temperature was the major determinant of fungal carbon use. Zak and Wildman [68] indicated that despite soil temperature being a major environmental characteristic in desert ecosystems, the majority of soil fungi are adapted to a mesophilic lifestyle. Rather, saprophytic fungi have adapted life history strategies that allow them to succeed through extreme heat conditions that exist in hot arid systems [3].
These carbon-use patterns demonstrate the resilience of soil bacteria and fungi to environmental stress in this arid system, as both soil bacteria and saprophytic fungal assemblages were able to quickly respond to substantial moisture windows regardless of prior environmental conditions. However, the activity of saprophytic fungi in this arid system declined with increased temperatures, as fungi were more active during early spring than late summer. The soil fungi during the summer months only respond to large precipitation events and subsequent available soil moisture increases, as was observed in September 2006 after intense rainfall events. Soil bacterial activity is highly responsive to levels of soil moisture, nitrogen, and soil organic carbon. Therefore, bacterial activity is tightly linked with soil carbon resulting from plant inputs and fungal activity (via decomposition and mineralization). Consequently, as increasing temperatures change soil moisture dynamics in this desert grassland, soil bacterial activity is likely to decline as well.
Although bacteria may be able to function more effectively than fungi at higher soil temperatures, global warming is likely to initiate declining windows of opportunity for both bacterial and fungal activity, which can ultimately lead to limited soil organic matter and soil nutrient levels in this system for above- and below-ground utilization. This observation presents a prospective scenario of how the environment regulates soil bacterial and fungal species in this system, and how higher trophic dynamics in this arid system may be greatly disrupted by a change in climate. In this region, global climate change over the next 50 years is predicted to increase temperatures by 3–5 °C, which will consequently result in increased storm magnitudes and intra-seasonal climate variability, potentially altering current seasonal precipitation by as much as 25%. Changing moisture and temperature dynamics in this region are likely to greatly alter soil microbial activity, which could change the soil functional dynamics in this region by affecting both carbon and nitrogen cycling, ultimately disrupting above-ground processes, which has repercussions for both below- and above-ground microbe and plant successes.
References
Noy-Meir I (1973) Desert ecosystems: Environment and producers. Ann Rev. Ecolog Syst 4:25–51
Cui M, Caldwell M (1997) A large ephemeral release of nitrogen upon wetting of dry soil and corresponding root responses in the field. Plant Soil 191:291–299
Zak JC, Sinsabaugh R, MacKay W (1995) Windows of opportunity in desert ecosystems: Their implications to fungal community development. Can J Bot 73:S1407–S1414
Reynolds JF, et al. (2004) Modifying the ‘pulse-reserve’ paradigm for deserts of North America: precipitation pulses, soil water, and plant responses. Oecologia 141:194–210
Schwinning S, Sala O (2004) Hierarchy of responses to resource pulses in arid and semi-arid ecosystems. Oecologia 141:211–220
Ryel RJ, et al. (2004) Water conservation in Artemisia tridentata through redistribution of precipitation. Oecologia 141:335–345
Schwinning S, Starr BI, Ehleringer JR (2003) Dominant cold desert plants do not partition warm season precipitation by event size. Oecologia 136:252–260
Austin AT, et al. (2004) Water pulses and biogeochemical cycles in arid and semiarid ecosystems. Oecologia 141:221–235
Kieft TL, et al. (1998) Temporal dynamics in soil carbon and nitrogen resources at a grassland-shrubland ecotone. Ecology 79(2):671–683
Cable JM, Huxman TE (2004) Precipitation pulse size effects on Sonoran Desert soil microbial crusts. Oecologia 141:317–324
Huxman TE et al. (2004) Response of net ecosystem gas exchange to a simulated precipitation pulse in a semi-arid grassland: the role of native versus non-native grasses and soil texture. Oecologia 141:295–305
Hadley (1994) Hadley Centre for Climate Predictions and Research
Groffman PM, Zaady E, Shachak M (2005) Microbial contributors to biodiversity in deserts. In: Shachak M (ed) Biodiversity in drylands. Oxford University Press, New York, NY, pp 109–121
Belnap J, et al. (2005) Linkages between microbial and hydrologic processes in arid and semiarid watersheds. Ecology 86(2):298–307
Nannipier P, et al. (2003) Microbial diversity and soil functions. Eur J Soil Sci 54:655–670
Parker LW, et al. (1984) Carbon and nitrogen dynamics during the decomposition of litter and roots of a Chihuahuan desert annual, Lepidium lasiocarpum. Ecol Monogr 54:339–360
Schlesinger WH, Fonteyn PJ, Marion GM (1987) Soil moisture content and plant transpiration in the Chihuahuan Desert of New Mexico. J Arid Environ 12:119–126
Steinberger Y, et al. (1999) Phospholipid fatty acid profiles as indicators for microbial community structure in soils along a climatic transect in the Judean Desert. Biol Fertil Soils 28:292–300
Fliesbach A, Sarig S, Steinberger Y (1994) Effects of water pulses and climatic conditions on microbial biomass kinetics and microbial activity in a Yermosol of the central Negev. Arid Soil Res Rehabil 8:353–362
Belnap J, et al. (2005) Soil biota can change after exotic plant invasion: does this affect ecosystem processes? Ecology 86(11):3007–3017
Widen B, Majdi H (2001) Soil CO2 efflux and root respiration at three sites in a mixed pine and spruce forest: Seasonal and diurnal variation. Can J For Res 31:786–796
Wall DH, et al. (2004) The need for understanding how biodiversity and ecosystem functioning affect ecosystem services in soils and sediments. In: Wall DH (ed) Sustaining biodiversity and ecosystem services in soils and sediments. Island, Washington, D.C, pp 1–12
Groffman PM, Bohlen PJ (1999) Soil and sediment biodiversity: cross-system comparisons and large scale effects. BioScience 49:139–148
Zhang Q, Zak JC (1998) Effects of water and nitrogen amendment on soil microbial biomass and fine root production in a semi-arid environment in west Texas. Soil Biol Biochem 30(1):39–45
Bonde TA, Lindberg T (1988) Nitrogen mineralization kinetics in soil during long-term aerobic laboratory incubations: A case study. J Environ Qual 17(3):414–417
Dou Z, et al. (1996) Soil nitrogen mineralization during laboratory incubation: Dynamics and model fitting. Soil Biol Biochem 28(4/5):625–632
Robertson GP, et al. (1999) Soil carbon and nitrogen availability: nitrogen mineralization, nitrification, and soil respiration potentials. In: Robertson GP (ed) Standard soil methods for long-term ecological research. Oxford University Press, New York, NY, pp 258–271
Knoepp JD, Swank WT (1998) Rates of nitrogen mineralization across an elevation and vegetation gradient in the Appalachians. Plant Soil 204:235–241
Hart SC, et al. (1994) Nitrogen Mineralization, immobilization, and nitrification. In: Page AL, Miller RH, Keeney DR (eds) Methods of soil analysis. Part 2, microbiological and biochemical properties. Soil Science Society of America, Madison, WI, pp 985–1018
Garland JL, Millis AL (1991) Classification and characterization of heterotrophic microbial communities on the basis of patterns of community-level sole-carbon-source utilization. Appl Environ Microbiol 57:2351–2359
Zak JC, et al. (1994) Functional diversity of microbial communities: a quantitative approach. Soil Biol Biochem 26(9):1101–1108
Zak JC, et al. (1997) Big Bend National Park watershed program monitoring microbial activity and diversity along an elevational gradient. In: 9th Conference on Research and Resource Management in Parks and on Public Lands. Albuquerque, NM
Dobranic JK, Zak JC (1999) A microtiter plate procedure for evaluating fungal functional diversity. Mycologia 91:756–765
Sobek E, Zak JC (2003) The soil FungiLog procedure: method and analytical approaches toward understanding fungal functional diversity. Mycologia 95:590–602
Konopka A, Oliver L, Turco RF (1998) The use of carbon substrate utilization patterns in environmental and ecological microbiology. Microb Ecol 35:103–115
Smalla K, et al. (1998) Analysis of Biolog GN substrate utilization patterns by microbial communities. Appl Environ Microbiol 64:1220–1225
MacLeod W (2002) Big Bend Vistas: a geological exploration of the Big Bend. Texas Geological Press, Alpine, TX
MacMahon JA, Wagner FH (1985) The Mojave, Sonoran and Chihuahuan Deserts of North America. In: Evenari M, Noy-Meir I, Goodall DW (eds) Ecosystems of the world: hot deserts and arid shrublands. Elsevier, New York, NY, pp 117–121
Larson P (1970) Deserts of America. Prentice-Hall, Englewood Cliffs, NJ, pp 12–16
Sowell J (2001) Desert ecology. University of Utah, Salt Lake City, UT
McClaran MP (1995) Desert grasslands and grasses. In: McClaran MP, Van Devender TR (eds) The desert grassland. University of Arizona Press, Tuscon, AZ, pp 3–24
Henry CD, Price JG (1984) Variations in caldera development in the tertiary volcanic field of the Trans-Pecos Texas. J Geophys Res 89:8765–8786
Aide M, et al. (2003) Geochemical indicators of external additions to soils in Big Bend National Park, Texas. Soil Sci 168(3):200–208
Turner AC (1997) Soil survey of Jeff Davis County, Texas. United States Department of Agriculture, Soil Conservation Service. p 3–12
Seager R, et al. (2007) Model projections of an imminent transition to a more arid climate in southwestern North America. Science 316:1181–1184
Johns TC, et al. (1996) The second hadley centre coupled ocean-atmosphere GCM: Model description, spinup and validation. Clim Dyn 13:103–134
Willig MR, et al. (1996) Functional diversity of soil bacterial communities in the Tabonuco forest: Interaction of anthropogenic and natural disturbance. Biotropica 28:471–483
Zak JC, Visser S (1996) An appraisal of soil fungal biodiversity: the crossroads between taxonomic and functional biodiversity. Biodivers Conserv 5:169–183
Miller RH, Keeney DR (1982) Methods of soil analysis, 2nd edn. Academic, Madison, WI
Sollins P, et al. (1999) Soil carbon and nitrogen. In: Robertson GP, Coleman DC, Bledsoe CS, Sollins P (eds) Standard soil methods for long-term ecological research. Oxford University Press, New York, NY, pp 89–105
Vance ED, Brookes PC, Jenkinson DS (1987) An extraction method for measuring soil microbial biomass C. Soil Biol Biochem 19(6):703–707
Nunan N, Morgan MA, Herlihy M (1997) Ultraviolet absorbance (280 nm) of compounds released from soil during chloroform fumigation as an estimate of the microbial biomass. Soil Biol Biochem 30(12):1599–1603
Jarrell WM, et al. (1999) Soil water and temperature status. In: Robertson GP (ed) Standard soil methods for long-term ecological research. Oxford University Press, New York, NY, pp 55–73
Onset CC (2004) Hobo-H8 Pro-series Users Manual. Bourne, MA: Onset Computer Corporation
Field A (2005) Discovering statistics using SPSS, 2nd edn. Thousand Oaks, CA.: Sage
Whitford W (2002) Conceptual framework and paradigms, in ecology of desert systems. Academic Press: San Diego, CA, pp 11–18
Schwinning S, et al. (2004) Thresholds, memory, and seasonality: understanding pulse dynamics in arid/semi-arid ecosystems. Oecologia 141:191–193
Belnap J, Phillips SL, Miller ME (2004) Response of desert biological soil crusts to alterations in precipitation frequency. Oecologia 141:306–316
Paul EA, Clark FE (1996) Dynamics of residue decomposition and soil organic matter turnover. In: Paul EA, Clark FE (eds) Soil microbiology and biochemistry. Academic, San Diego, CA
Appel T (1998) Non-biomass soil organic N-the substrate for N mineralization flushes following soil drying-rewetting and for organic N rendered CaCl2 extractable upon soil drying. Soil Biol Biochem 30:1445–1456
van Gestel M, Merckx R, Vlassak K (1993) Microbial biomass responses to soil drying and rewetting: The fate of fast- and slow-growing microorganisms in soils from different climates. Soil Biol Biochem 25:109–123
Zak JC, Freckman DW (1991) Soil communities in deserts: microarthropods and nematodes. In: Polis GA (ed) The ecology of desert communities. Arizona, Tuscon, AZ, pp 55–88
Vishnevetsky S, Steinberger Y (1997) Bacterial and fungal dynamics and their contribution to microbial biomass in desert soil. J Arid Environ 37:83–90
Parker LW, et al. (1984) Effects of simulated rainfall and litter quantities on desert soil biota: soil respiration, microflora, and protozoa. Pedobiologia 27:185–195
Wardle DA, Parkinson D (1990) Interaction between microclimatic variables and the soil microbial biomass. Biol Fertil Soils 9:273–280
Ross DJ (1987) Soil microbial biomass estimated by the fumigation-incubation procedure: seasonal fluctuations and influence of soil moisture content. Soil Biol Biochem 19:397–404
Kieft TL, Soroker E, Firestone MK (1987) Microbial biomass response to a rapid increase in water potential when dry soil is rewetted. Soil Biol Biochem 19:119–126
Zak JC, Wildman HG (2004) Fungi in stressful environments: inventory and monitoring methods. In: Mueller GM, Bills GF, Foster MS (eds) Biodiversity of fungi. Elsevier, Burlington, MA, pp 303–316
Acknowledgements
This research is funded by the USGS Global Climate Change Small Watershed Project, to J. Zak and a National Park Service grant, and to J. Zak and D. Tissue. Special thanks are extended to Joe Sirotnak along with the rest of the research staff at BBNP for continued support and cooperation.
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Bell, C., McIntyre, N., Cox, S. et al. Soil Microbial Responses to Temporal Variations of Moisture and Temperature in a Chihuahuan Desert Grassland. Microb Ecol 56, 153–167 (2008). https://doi.org/10.1007/s00248-007-9333-z
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DOI: https://doi.org/10.1007/s00248-007-9333-z