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Front. Microbiol., 11 October 2012
Sec. Terrestrial Microbiology
Volume 3 - 2012 |

Co-occurrence patterns of plants and soil bacteria in the high-alpine subnival zone track environmental harshness

Andrew J. King1*, Emily C. Farrer2, Katharine N. Suding2 and Steven K. Schmidt3
  • 1Ecosystem Sciences, Commonwealth Scientific and Industrial Research Organisation, Acton, ACT, Australia
  • 2Department of Environmental Science, Policy & Management, University of California at Berkeley, Berkeley, CA, USA
  • 3Department of Ecology and Evolutionary Biology, University of Colorado at Boulder, Boulder, CO, USA

Plants and soil microorganisms interact to play a central role in ecosystem functioning. To determine the potential importance of biotic interactions in shaping the distributions of these organisms in a high-alpine subnival landscape, we examine co-occurrence patterns between plant species and bulk soil bacteria abundances. In this context, a co-occurrence relationship reflects a combination of several assembly processes: that both parties can disperse to the site, that they can survive the abiotic environmental conditions, and that interactions between the biota either facilitate survival or allow for coexistence. Across the entire landscape, 31% of the bacterial sequences in this dataset were significantly correlated to the abundance distribution of one or more plant species. These sequences fell into 14 clades, 6 of which are related to bacteria that are known to form symbioses with plants in other systems. Abundant plant species were more likely to have significant as well as stronger correlations with bacteria and these patterns were more prevalent in lower altitude sites. Conversely, correlations between plant species abundances and bacterial relative abundances were less frequent in sites near the snowline. Thus, plant-bacteria associations became more common as environmental conditions became less harsh and plants became more abundant. This pattern in co-occurrence strength and frequency across the subnival landscape suggests that plant-bacteria interactions are important for the success of life, both below- and above-ground, in an extreme environment.


Interactions between plants and microorganisms play a central role in ecosystem functioning (Bonfante and Anca, 2009; Hayat et al., 2010). However, it has been difficult to characterize plant-microbial relationships for all but the most closely interacting species (Kremer, 2006; van der Heijden et al., 2008; Hayat et al., 2010). For example, while mutualistic and parasitic symbiotes inhabiting root tissue have been well studied (mycorrhizae: Bianciotto et al., 1996; Bonfante and Anca, 2009; diseases: Compant et al., 2005; Kremer, 2006; N-fixation: Hayat et al., 2010; heat tolerance: Márquez et al., 2007; plant growth hormone production by bacteria: Hayat et al., 2010), it appears that these interactions just scratch the surface of the probable range of symbioses (Li and Kremer, 2006; Rudgers et al., 2012). Similarly, the indirect associations involved with decomposition and nutrient cycling between microorganisms and plants, despite being well studied from a biogeochemical perspective, have remained difficult to characterize with respect to the soil microbial species involved (van der Heijden et al., 2008). In addition to the difficulty imposed by frequent findings of new plant-bacteria interactions, predicting the frequency and types of known plant-soil microbe associations is often difficult even when species lists and environmental conditions are known (Bever et al., 2010). The success of targeted studies using cultures (Kremer, 2006; Hayat et al., 2010) and stable isotope probing (Haichar et al., 2008) to identify plant-soil interactions suggests that larger scale surveys using high-throughput methods may allow for the detection of broad patterns for plant-soil microbe interactions from bulk soil. Here, for the first time, we use culture-independent methods to test hypotheses regarding the drivers of co-occurrence relationships between plants and soil bacteria in bulk soil samples and at the landscape scale.

The co-occurrence of species that share resource requirements is governed by competitive (Diamond, 1975) and facilitative (Bruno et al., 2003) interactions between species as well as independent environmental sorting in the case of strong environmental filters (Weiher and Keddy, 1995; Diaz et al., 1998; Ackerly, 2003). As such, co-occurrence patterns represent an important tool for inferring potential interactions involving microorganisms, particularly bacteria, which are most commonly identified indirectly via isolation of organisms or sequencing their DNA from soil extracts (Ruan et al., 2006; Horner-Devine et al., 2007; Fuhrman and Steele, 2008; Freilich et al., 2010; Barberán et al., 2012). Because the methods enabling the analysis of high-throughput, sequencing based, broad-scale surveys of bacteria are very new (Caporaso et al., 2011; Gonzalez et al., 2011), the frequency and strength of plant-bacteria co-occurrence relationships at a landscape scale are poorly understood. Thus, high-throughput sequencing of bulk soil samples represents a potentially powerful resource for the detection of plant-bacteria interactions such as saprotrophic bacteria that specialize on senesced material from a particular plant species, bacteria sharing similar environmental preferences, and symbiotic rhizosphere bacteria which are often found to be a well represented subset of bulk soil samples (Mahaffee and Kloepper, 1997; Graff and Conrad, 2006; Berg and Smalla, 2009).

We examine plant-bacterial co-occurrence relationships along an abiotic harshness gradient in a high-alpine subnival ecosystem because the resulting gradient in plant abundance represents increasing availability of reduced carbon for soil microorganisms (Ley et al., 2004) and the oligotrophic soils mean plant symbioses with soil microorganisms are particularly important (Chapin et al., 1994; Tscherko et al., 2005). The harsh environmental conditions of the subnival zone result from high altitudes with their concurrent high solar radiation, low humidity, large daily temperature fluctuations that often cross the freezing point, large snowpack volumes or high wind exposure, and low soil nutrients (Ley et al., 2004; Freeman et al., 2009; King et al., 2010). Thus, subnival organisms must persist in a state of strong environmental stress which prohibits continuous plant cover, but is not extreme enough that there is year-round snow or ice cover. Previous studies in slightly less harsh, alpine ecosystems have shown that the majority of plants are able to form mutualistic associations with fungi, N-fixing bacteria, and growth promoting bacteria (Mullen et al., 1998; Cazares et al., 2005; Sheng et al., 2010), suggesting that mutualistic associations are important for the survival of plants and bacteria in these systems (Hobbie et al., 2005; Wang and Qiu, 2006; Schmidt et al., 2008a; Sheng et al., 2010; Zinger et al., 2011). However, in subnival glacial fore-fronts these same well-colonized plant species often lack root mutualistic symbionts and this lack of symbionts is thought to be due to dispersal limitation of the microorganisms in the newly exposed substrate (Cazares et al., 2005). Pathogens of alpine plants, on the other hand, are rarely reported (Olofsson et al., 2011); it may be that pathogens are rare or it could be that few studies explicitly focus on this group. Thus, positive plant-bacterial interactions are of high potential importance in subnival landscapes.

We draw from the body of theory regarding community assembly (Diamond, 1975; Chapin et al., 1994; Chase and Leibold, 2003; Reynolds et al., 2003) to develop simple yet fundamental hypotheses about the drivers of the frequency and distribution of plant-bacteria co-occurrence relationships. A basic tenet of community assembly theory is that abiotic and biotic “filters” select species from the regional species pool to assemble a local community most suited to the prevailing conditions in a process known as ecological sorting (Weiher and Keddy, 1995; Diaz et al., 1998; Ackerly, 2003). In the context of plant-bacteria co-occurrence in the alpine subnival environment, we expect the presence of biotic filters that restrict one group to occur only when its symbiont/facilitator is present as well as a common set of abiotic and dispersal filters that may constrain both plants and microbes directly. Biotic filters may be reflected by bacteria with plant growth promoting/inhibiting abilities or plants that promote the growth of mutualistic soil bacteria. If certain bacteria and plants have similar environmental preferences, they may co-occur across space independently without directly interacting with each other. For soil bacteria that are, in fact, interacting with plant species, negative correlations can arise from inhibitory and competitive interaction whereas positive correlations can arise from facilitative, mutualistic, or parasitic interactions.

Based on this community assembly framework, we explicitly test three hypotheses about the drivers of the frequency and distribution of plant-bacteria co-occurrence relationships. First, analogous to the suitable habitat area-diversity relationship from island biogeography (MacArthur and Wilson, 1967; Martiny et al., 2006), we expect bacteria to more often co-occur with plant species’ that provide larger and more consistent nutrient sources across the landscape. Assuming that a plant species contribution to nutrient pools is proportional to its abundance (Grime, 1998; Vile et al., 2006), we thus predict that abundant plants will have more bacterial clades associated with them than less abundant plants.

Second, we expect that bacterial clades related to isolates with plant growth promoting/inhibiting abilities will show stronger species-specific associations with plants than will bacteria related to isolates with plant-independent metabolic strategies. Thus, the hypothetical functional capacity for associating with a plant species represents a biotic filter (e.g., Chase and Leibold, 2003) for the occurrence of bacteria in the subnival landscape. Importantly, evaluation of this driver is also testing the utility of a correlation approach using culture-independent environmental sequencing of the 16S to identify clades that have a specific function.

Lastly, we predict that facilitation should be more common in portions of the landscape furthest from intact tundra due to increasing environmental harshness. Importantly, theory predicts that facilitative and mutualistic plant-microbe interactions are more common in harsher, low density, low nutrient availability, successional environments (Reynolds et al., 2003) because they promote the growth of both bacteria and plants. Such facilitative interactions are thought to be able to overcome environmental filters that would otherwise exclude either symbiont (Choler et al., 2001). Although it is likely endemic extremophiles are adapted to the harsh environment of the subnival zone, our previous work has shown that the ancestry of bacteria does not change significantly across the landscape (King et al., 2010). Therefore, we expect that the lower temperatures, greater UV radiation, and less soil nutrients with increasing remoteness (Körner, 2007) represent real increases in stress to bacteria in this landscape.

Materials and Methods

Study Site

The dataset used in this analysis comes from a previously published spatially explicit study of the Niwot Ridge LTER’s south-facing subnival slope (eastern face of the Continental Divide in Colorado, USA; Figure 1; King et al., 2010). This slope is covered with snow from October to June and the deepest snow fields do not melt fully until August. Precipitation averages 930 mm/year with 80% falling as snow (Nemergut et al., 2005). The study area extends over 2 km2 and is predominately covered by granite blocks greater than 1m in diameter. Interspersed are patches of soil up to 20 m in diameter with plant cover ranging from 0% in late melting snowbanks up to 100% in a few exposed areas receiving water from upslope snowmelt. Plants in this environment are 10–20 cm in height and have approximately the same biomass per individual.


Figure 1. Our 76 sample sites in the subnvial zone of the Green Lakes Valley within the Niwot Ridge LTER study site on eastern face of the Continental Divide in Colorado, USA (red outline represents the south-facing extent of exposed soils). From the north-east corner to the north-west corner of the study area is 2 km. These sites represent a subset of the sites in our previous study (shown in Figure 1 of King et al., 2010).

Plant Species and Soil Sampling

As previously reported (King et al., 2010), sampling locations were chosen based on a pilot study (King et al., 2008) in order to provide optimal spacing for the calculation of spatial autocorrelation models across the landscape. Sampling was partitioned into a grid of 160 samples across the landscape, spaced every 50 m, with three targeted 30 m × 30 m areas sampled at every 5 m (Figure 1 in King et al., 2010). In September of 2007, at each sampling location a pen was tossed into the air and at the spot where it landed all vascular plants within a 3 m2 circle were identified and a soil sample was collected. Plant abundance measures were based on stem counts. Because alpine species are constrained to a low stature growth form, stem counts are an appropriate estimate of species biomass within a plot (Grytnes, 2000). Species identification was based on Webber and Whittmann (2001).

Soils samples were collected by homogenizing a ∼50 cm2 patch of soil in situ to a depth of 4 cm and then filling a 50 mL sterile conical tube with soil. Because of the high degree of spatial autocorrelation in bacterial community diversity in this system, an individual sample is likely to be highly representative of the surrounding 25 m2 of soil (King et al., 2010). Samples were transported to the lab within 5 h of collection, held at 4°C for up to a week while subsampling for soil biogeochemistry was conducted (results presented in King et al., 2010), and afterward frozen at −20°C until DNA could be extracted (up to 9 months). 85 of the original 160 samples were randomly selected for bacterial community analysis. From those 85 samples, we include in the current study only plots that had at least two plants per m2 (76 samples, Figure 1).

Bacterial Community Assessment

Bacterial community composition was also measured as described in King et al. (2010). Briefly, for each of the 76 soil samples, DNA was extracted from 1 g of soil using a Mobio PowerSoil DNA Isolation Kit (Mobio Laboratories) and PCR was used to amplify the V1–V2 hypervariable region of the bacterial 16S SSU ribosome gene using the 27F and 338R primers and protocol from Fierer et al. (2008). Sequencing was performed on the Roche 454 platform using FLX chemistry. Raw sequence data was processed using the methods of Hamady et al. (2010), resulting in 6151 representative OTUs at 3% similarity with 10,000 total reads and an average of 200 reads per sample. For downstream analysis, sequence reads of each OTU in each sample were converted to relative abundance by dividing by the total number of sequences in an individual sample.

Selection of Clades Using Correlation Strength with Plant Species Abundances

Because most methods of assigning taxonomic IDs to individual sequences are based on the extent of knowledge contained in a reference database (e.g., DeSantis et al., 2006; Wang et al., 2007) and because classical taxonomies can be polyphyletic, we used a phylogenetic tree to assign sequences to clades for downstream analysis (the phylogenetic tree was the same as used in King et al. (2010)). This approach is essentially a phylogenetic comparative method (Harvey and Pagel, 1991) with association with plants as the trait of interest. Initially we considered as candidate clades all nodes on the tree that had greater than 1% of the sequences (therefore, clades are independent of phylogenetic resolution and a particular clade might correspond to any gradation between phylum and species). Each candidate clade’s relative abundance per sample was then regressed against the abundances of the 13 most prevalent plant species (all plant species averaging greater than one individual per sampling location; the total plant species pool for this landscape is 26). Regressions were performed in R using the Akaike Information Criterion (Akaike, 1974) to select the plant species with the most explanatory power via the step and lm functions (R Development Core Team, 2011). A strictly linear approach was chosen to maintain a low number of parameters and residuals from both the models, and pairwise regressions of clades against individual plant species were found to be normally distributed.

The initial list of clades was then filtered so that clades were mutually exclusive; this filtering was achieved via sorting the clades by r2, removing all clades that had a lower r2 but shared sequences with a clade that had the highest r2, and then reiterating with the next highest remaining r2 until reaching a clade without a significant correlation or an r2 less than 0.15. The remaining 22 clades were tested for significance with an ANOVA with the AIC selected variables as explanatory variables and significance cutoff adjusted for multiple comparisons using the Bonferroni correction for n = 22 comparisons (p < 0.002; Bonferroni, 1936). The final result was 14 bacterial clades. Taxonomic IDs were then assigned as the finest resolution at which at least 50% of the sequences shared the same classification in their closest match in NCBI GenBank.

Plant-Bacteria Co-Occurrence Ordination

To visualize the correlations between plant species and the bacterial clades identified by the above regressions we used a NMDS approach. First, we constructed a correlation matrix with all possible pairwise comparisons between both bacteria clades and plant species. We then used a common approach (Cox and Cox, 1994) to transform each Pearson correlation value (ranging from 1 to −1) by taking the absolute value and subtracting it from one such that both positive and negative 100% correlations became a distance of 0 and a 0% correlation became a distance of one. The resulting distance matrix was used as an input to the metaMDS function in the vegan package for R (Oksanen et al., 2010). While co-occurrence networks in microbiology have most commonly been arranged so that the nodes with the greatest numbers of edges are in the center of the plot (Barberán et al., 2012), NMDS is very commonly used in plant ecology to represent strength (rather than number) of interactions (McCune et al., 2002). We chose NMDS so that the strength of interaction between each clade or plant species in the dataset would be represented by proximity. In addition, we used NMDS to ordinate our plant-bacteria co-occurrence relationships rather than the more common metric MDS approach (Cox and Cox, 1994) because NMDS gives greater weight to the strongest correlations (Cox and Cox, 1994) and relatively little weight to weaker correlations (MDS techniques would have used the raw correlation value and the large number of non-significant correlations with values of 0.20 or less would have introduced extra noise into the ordination). After the species and clades were ordinated, we visually overlaid the significant interactions according to our models.

Statistical Analysis

To quantitatively estimate the average strength of association for a particular plant species or bacterial clade, we averaged the individual correlation r values (absolute value) that were significant according to our AIC supervised linear models. (p < 0.05, two-tailed t-test for each regression coefficient not equal to 0). Bonferroni correction of the p-value for multiple comparisons was done for each model’s coefficient significance tests (clade relative abundance models ranged from one to eight AIC selected plant species, Supplementary Materials).

To address the hypothesis that more abundant plants are better predictors of the abundance of associated bacterial clades, the number of significantly correlated clades per plant species was regressed against plant species abundance and we used a t-test to determine if the correlation was significantly greater than zero. The mean correlation strength of clades associated with each plant species was also regressed against plant species abundance and we used a t-test to determine if the correlation was significantly greater than zero. These tests were performed both including and excluding plant species with no significantly correlated bacterial clades.

To address the hypothesis that average association strength would be greatest for bacterial clades closely related to bacterial species that are known to form symbioses with plants, we performed a t-test comparing mean correlation strengths of each model’s significant factors for clades related to plant symbiosis capable versus plant-independent bacteria [i.e., Avg Corr Str (r) column of Table 1].


Table 1. A summary of known metabolic capabilities, OTU richness, number of significant plant-associations, and model fits for plant-associated subnival zone bacterial clades.

To address the hypothesis that environmental harshness affects association strength, we reweighted all already identified sets of bacterial clade relative abundances by a harshness index (a proxy for the subnival landscape’s general gradient of increasing exposure, temperature variability, and time before complete snowmelt with increasing distance away from intact tundra). The environmental harshness index for each sample was calculated as distance from intact tundra + distance from valley floor. In addition to distance from tundra and altitude, the degree of shelteredness from wind is also expected to play a role in structuring species co-occurrence in this subnival landscape (Litaor et al., 2008). However, although both high and low snow accumulation areas vary in the nature of the primary stressor (late snowmelt versus high wind exposure), snowfields and windswept areas occur throughout our study area (Erickson et al., 2005). Due to this variability, our harshness metric is not correlated with snow depth (Correlation test, p = 0.2, r2 = 0.02) in the Niwot subnival zone, suggesting that harshness overlays a matrix of sheltered and unsheltered areas which occur throughout the landscape. Thus, our proposed harshness metric is similar in nature to altitudinal gradient analysis in that it is strongly correlated with gradients in temperature/solar insolation that overlay landscape heterogeneity in shelteredness (Körner, 2007).

We examined the effect of multiplying abundances by the harshness index (up-weighting harshness). We also examined the effect of multiplying abundances by the harshness subtracted from the max harshness value (down-weighting harshness). For up- and down-weighted datasets we recalculated linear model fits for each of the previously identified bacterial clades using AIC selection of significantly predictive plant species. The effect size of reweighting was then calculated by averaging the individual correlation r values (absolute value) between plant species and bacterial clades that were significant first for the upweighted and then for the down-weighted datasets. To test if a significant effect of up- or down-weighting was observed for a specific clade, we used an ANOVA with the AIC selected variables as explanatory variables and significance cutoff adjusted for multiple comparisons using the Bonferroni correction for n = 14 comparisons (p < 0.004; Bonferroni, 1936). Again, the clade average correlation strengths reflect only significant correlations after Bonferroni correction for each model’s set of AIC selected variables.


General Findings

The NMDS ordinated co-occurrence network contained 14 bacterial clades, representing 31% of the total sequences in our study, and 10 of the 13 plant species (Figure 2). Significant correlations were not dependent on the diversity of bacterial OTUs, total branch length within the clade, or relative abundance of clades (Figure 3). The percentage of variance in clade relative abundance significantly explained by plant species abundance ranged from 40% to our minimum cutoff of 15% (Table 1). Negative correlations, at 3, were less common than positive correlations, at 14 (Figure 2; Table 1). Bacterial clades had one or two significantly correlated plant species; only one had exclusively negative significant correlations with plant species (Desulfovibrionales), and two had multiple positive associations (Clostridiales and Rhodospirillales). Our models predicting bacterial clade relative abundance based on plant species abundance with 13 potential explanatory plant species (Datasheet S1 in Supplementary Material) only slightly under-perform compared to previously published environmental models for the three most spatially structured clades examined by King et al. (2010) with 21 potential explanatory variables; on average our models explain 28% of variance in clade relative abundance for Rhodospirillales, Rhizobiales, and Acidobacteria Gp4, compared to 40% for the previously published (King et al., 2010) models using plant abundance, soil biogeochemistry, and spatial autocorrelation as predictors.


Figure 2. A NMDS (stress = 0.292) ordinated co-occurrence network based on the correlation matrix (absolute values of Pearson r) for 10 plant species abundances and 14 bacterial clade relative abundances (Datasheet S4 in Supplementary Material). Overlaid are lines designating significant model-based interactions between a plant species and bacterial clade with solid for positive and dashed for negative interactions (thin lines represent two-tailed t-test for model coefficient significance, p < 0.05; thick lines represent significance after Bonferroni correction for multiple comparisons). Because this is an ordination of the correlation matrix, proximity of points to one another represents higher correlation between their abundances across the subnival landscape.


Figure 3. A phylogenetic tree showing the clades correlated with plant abundance. Green clades are commonly found associated with plants in the scientific literature (Table 1). Orange clades have no known symbiotic association with plants. Gray clades are only known from environmental sequencing. Wedge size is proportional to the number of 3% OTU clusters in a clade.

Six of the 14 bacterial clades (comprising 10% of the total sequences) are related to isolates that are known for forming symbioses with plants (Table 1) for N-fixation and/or plant growth promotion: Rhizobiales, Rhodospirillales, Clostridiales, Desulfovibrionales, Pseudonocardiaceae, and Burkholderiales (also pathogenic) in addition to their capacity of free-living heterotrophic functions (Table 1). Many of these clades are also related to isolates known to be able to perform rhizosphere-independent soil functions such as sulfur reduction (Rhodospirillales, Desulfovibrionales) and sulfite oxidation (Clostridiales, Pseudonocardiaceae). Two of the clades (comprising 9% of the sequences) lacked support for plant symbiosis capability and displayed a diverse array of metabolic strategies: carbon monoxide oxidation (Ktedonobacteraceae), general heterotrophy/sulfate + iron reducing (Deltaproteobacteria). Five of the remaining six clades (comprising 11% of the total sequences) represent common soil bacteria with no cultured representatives and largely unknown functions (four clades of Acidobacteria, TM7). The last clade, Acidimicrobiaceae, is defined by their autotrophic growth by oxidizing ferrous iron, but has been hypothesized to also inhabit the rhizosphere and root tissue based on culture-independent surveys (Stafford et al., 2005; Qin et al., 2012) and may have the capacity for nitrogen fixation (Buckley et al., 2007).

H1: abundant plants will have more bacteria associated with them than less abundant plants because they represent the most common plant-derived nutrient source

At first inspection, plant species abundance was not correlated to the number of correlated bacterial clades (r = 0.45, two-tailed t-test for rho = 0: p = 0.14, Table 2) or the average correlation strength for clades associated with a particular plant species (r = 0.25, two-tailed t-test for rho = 0: p = 0.44, Table 2). However, when plants with no correlated clades were removed from the analysis, there was a significant relationship between plant abundance and average correlation strength for clades associated with a particular plant species (r = 0.88, two-tailed t-test for rho = 0: p = 0.004, Figure 4B) and a weakly significant correlation for the number of correlated bacterial clades (r = 0.67, one-tailed t-test for rho = 0: p = 0.0275, Figure 4A). The plants with the greatest number of positive associations were Geum rossii (four associations), Kobresia myosuroides (two associations), and Carex nardina (two associations). Abundant plant species lacking significantly correlated bacterial clades were Bryophytes, Trisetum spicatum, Trifolium nanum, Silene acaulis.


Table 2. A summary of subnival zone plant species’ abundances, number of significant bacterial clade-associations and model fits.


Figure 4. Regressions of plant abundance versus total number of significant associated bacterial clades (A) or average strength of the correlations for associated bacterial clades (B). Regression lines are significant if the plant species without any significant associated bacterial clades are excluded from the analysis [r = 0.67, one-tailed t-test for rho = 0: p = 0.0275 (A); r = 0.88, two-tailed t-test for rho = 0: p = 0.004 (B)].

H2: potentially plant symbiosis capable bacterial clades will have greater average correlation strength with plant species than clades predicted to lack the capacity for symbiosis

On average, bacterial clades related to strains that were capable of forming symbioses with plants did not differ significantly in their average association strength from bacterial clades without known symbiosis capability (mean r was 0.34 symbiosis capable versus 0.29 incapable, two-tailed t-test: p = 0.63; Table 1). Of the bacterial clades with assignable functional capacities (Figure 3, Table 1), the Burkholderiales had the strongest association with a plant species (G. rossii; Figure 2; Datasheet S4 in Supplementary Material). Furthermore, two relatively poorly understood clades, the Acidobacteria Gp4 and the TM7, were similarly strongly associated with plant species (Table 1). The primary distinction between the two groups of clades related to strains with known function was that putatively plant symbiosis capable bacteria clades had lower within clade sequence richness than plant-independent clades (mean OTU richness was 93 for plant-dependent versus 411 for plant-independent, two-tailed t-test: p = 0.005).

H3: more remote sites will have fewer but stronger associations between plant species and bacterial clades because facilitation should be more common with increasing environmental harshness

There were only two bacterial clades that had significant models only in the harshness upweighted dataset the Rhodospirillales, and Pseudonocardiaceae (Figure 5A; Datasheet S2 in Supplementary Material; Table 1). The Rhodospirillales also increased its association strength with the dicots E. scriberneri and C. phaeocephala when environmental harshness was upweighted (Table 1). Similarly, the Actinobacterial clade, Pseudonocardiaceae, increased its association strength with the plants F. rubrum and C. phaeocephala when harsh sites were upweighted. On the other hand, 7 of the 14 clades had significant model fits only in less harsh sites (sites proximal to the continuous tundra were upweighted; Figure 5B; Datasheet S3 in Supplementary Material; Table 1). Although there were fewer bacterial clades significantly co-occurring with plants in harsh portions of the landscape there was no significant difference in the average correlation strength with plant abundances versus clades preferring less harsh locations (0.42 versus 0.44, two-tailed t-test, p = 0.60).


Figure 5. NMDS ordinated co-occurrence networks based on the correlation matrix after reweighting our clade relative abundances by a harshness metric. (A) For harshness upweighted there were nine plant species and seven bacterial clades which were significantly co-occurring (stress = 0.227). (B) For harshness down-weighted there were nine plant species and 12 bacterial clades which were significantly co-occurring (stress = 0.245). Overlaid are lines designating significant model-based interactions between a plant species and bacterial clade with solid for positive and dashed for negative interactions (thin lines represent two-tailed t-test for model coefficient significance, p < 0.05; thick lines represent significance after Bonferroni correction for multiple comparisons). Because this is an ordination of the correlation matrix, proximity of points to one another represents higher correlation between their abundances across the subnival landscape.

Plants species had the greatest number of associations in places where they were most abundant (Table 2). For example, G. rossii decreased in abundance with distance from tundra and its correlations with bacterial clades were entirely dependent on associations in sites proximal to the tundra. The number of plant-bacteria associations was lower in harsher portions of the landscape (22 associations near tundra versus 12 near snowline) but the average correlation strength per plant species did not differ between harshness upweighted and downweighted datasets (0.31 versus 0.40; two-tailed t-test p = 0.42).


This study is the first demonstration, to our knowledge, of plant species and soil bacterial associations across a heterogeneous landscape with a diverse plant community and indicates that plant-bacteria interactions are a key potential driver of the structure of the subnival ecosystem. In fact, 31% of bacterial sequences in this study fell into clades whose relative abundance was significantly correlated to plant species abundance. This percentage represents the presence in bulk soil material of rhizosphere symbiotes, decomposers that grow particularly well on senesced material from the associated plant, and independent bacteria sharing similar environmental preferences (Mahaffee and Kloepper, 1997; Graff and Conrad, 2006). That the percentage of bacteria correlated with plant species abundance in subnival soil is not greater likely reflects the fact that surveys of bulk soil detect a limited percentage of plant-bacteria symbiotes relative to direct analysis of plant roots (Mahaffee and Kloepper, 1997; Graff and Conrad, 2006). Yet it remains to be seen if studies of bulk soils in less extreme landscapes will find similar percentage of their sequences associated with plant species abundances. Importantly, the associations between plant species and bacteria were not evenly distributed across the subnival environment, but showed clear differences in strength and frequency between environmentally harsh sites close to the snowline and the less harsh sites close to continuous tundra (Table 1). The examination of our three hypothesized drivers of community assembly in this landscape (plant abundance, clade potential functional capacity, and environmental harshness) helps place these plant-bacteria co-occurrence patterns for subnival soils in a broader context.

The first of our hypothesized assembly drivers, plant abundance, was thought to influence the distributions of soil bacteria. Although in general plant abundance was not correlated with the number of associated clades in this subnival landscape, the subset of plants that had significant correlations with bacterial clades showed a strong relationship between abundance and mean clade correlation strength as well as number of clades (Figure 4; Table 2). This suggests that abundant plants are good predictors of the bulk soil relative abundance of both generalist plant-dependent bacteria and bacteria directly specializing on the micro-environment created by a plant species. An analogous situation occurs in glacial recession landscapes wherein bacterial diversity increases along with successive plant colonization although only a subset are specifically associated with individual plant species (e.g., Schmidt et al., 2008b; Knelman et al., 2012). While the plant with the greatest number of positive associations, G. rossii, was indeed the most abundant plant species, K. myosuroides and C. nardina had the second highest number of positive associations even though they are only sparsely distributed across this subnival landscape. Interestingly, while G. rossii is dominant in moist meadow tundra at Niwot Ridge (Bowman et al., 2004), K. myosuroides and Carex species are dominant in dry meadow tundra ecotypes (Fisk and Schmidt, 1995; Seastedt and Vaccaro, 2001). Dominance is not the only important factor here, however, as the co-dominant with G. rossii, D. caespitosa, did not have a large number of associated bacteria. Digging deeper, both G. rossii and K. myosuroides are known to associate with soil microorganism in oligotrophic conditions (Lipson et al., 2002; Bowman et al., 2004) whereas D. caespitosa is thought to prefer higher nutrient soils and may have weaker associations with soil microorganisms (Bowman et al., 2004). Thus, bacterial clades may co-occur with plants not just based on the abundant plants in a specific environment but also based on the plant species’ level of interaction with soil bacteria. This revised hypothesis, that the life history of abundant plants drives association number, is similar to previous observations that bacterial clades associated with plant community types in less extreme environments (e.g., Berg and Smalla, 2009; Eskelinen et al., 2009; Bezemer et al., 2010) and suggests that the signature of plant dominance on co-occurring soil bacterial clades should have transferability across ecosystems.

Clade functional capacity, our second hypothesized driver of assembly, tests the assumption that previously reported functional niche characteristics for bacterial clades predict patterns co-occurrence with plants (i.e., functional niche assembly, Chase and Leibold, 2003). Six of the eight clades that were related to cultured isolates, representing 10% of the sequences in our study, were closely related to strains previously reported to form mutualistic associations with plants; however, these clades did not have a stronger average correlation with associated plants than the other clades in our study (Table 1). However, the two bacterial clades we categorized as likely to be plant-independent were the largest clades in our study (themselves representing 10% of the total sequences) and are known only for their function as generalist soil heterotrophs (Table 1). This difference in diversity between our clades related to previously cultured strains supports the idea that functionally relevant clades (or Operational Taxonomic Units) can be successfully identified using a phylogenetic comparative method to selecting the nodes on a phylogenetic tree of environmental sequences with the greatest correlation to a factor of interest (co-occurrence with plants in this study). Thus, if our assignment of association type is accurate, the strength and likely the specificity of associations may differ within both symbiotic and non-symbiotic soil bacterial guilds; for example, soil heterotrophs have been shown to strongly specialize on a particular plant’s litter or non-specifically attack any detritus (van der Heijden et al., 2008), and symbiotic bacteria have been shown to opportunistically infect a plant but also commonly grow as a free-living form (Rodrigues-Diaz et al., 2008). Therefore, although strength of correlation is not a strong predictor of the type of plant-bacterial associations, clades related to plant-symbiotic bacteria may be more likely to correlate with plant species abundances and with a finer taxonomic resolution than clades related to free-living bacterial species.

An additional note on the potential selection for specific bacterial functions is that only one bacterial clade had only negative significant correlations with plants in this subnival ecosystem – the Desulfovibrionales (1.3% of the total sequences). In the context of correlations, negative interactions could mean either inhibition either from disease and competition or an indirect link via differential response to an environmental gradient. For the subnival ecosystem, the presence of a significant area of exposed soils and microbial crusts selects for bacteria that are adapted to the plant-free state (Nemergut et al., 2007; Freeman et al., 2009) and these crust bacteria should show a negative association with abundant plant species (i.e., fewer plants = more crust bacteria). That so few clades displayed this pattern suggests inhibition between bacteria and plants is rare in the subnival zone, which is in agreement with previous hypotheses about facilitation being the primary driver of species interactions in early successional systems (Chapin et al., 1994; Walker and del Moral, 2003).

Termed environmental harshness, the last of our three hypothesized drivers of subnival soil community assembly is based on the theory that abiotic factors create a selective filter for plant-bacterial associations (Weiher and Keddy, 1995; Diaz et al., 1998; Ackerly, 2003) with fewer but stronger associations under harsher conditions (Callaway and Walker, 1997; Reynolds et al., 2003; Seeds and Bishop, 2009). Within the subnival landscape of Niwot Ridge, there were six significant models in the remote-upweighted dataset whereas there were 12 significant models in the remote-down-weighted dataset. Moreover there were only two bacterial clades that had a significant model fit in only the most environmentally harsh sites (Table 1). This is in agreement with the hypothesis that plant-microbe interactions are less frequent in the more remote portions of the subnival landscape as a result of less plant diversity and low abundance of plant-symbiotic bacteria (Seeds and Bishop, 2009). With these harsh conditions, it is also hypothesized that interactions should be stronger (Reynolds et al., 2003), yet, there was no significant difference in the average correlation strength for clades favoring one end of the harshness gradient or the other. This lower number of harshness upweighted plant-bacteria correlations and similar strength of correlation despite the high correlation of individual plant species with our harshness gradient suggests that environmental filters become more important than biotic filters in harsher environments and is in agreement to what previous work has found at the community scale (Carlson et al., 2012).

Interestingly, both of the bacterial clades that were remote specialists are related to isolates known to garner energy from non-organic sources; members of the Rhodospirillales have demonstrated the ability to perform anaerobic phototrophic sulfate reduction in addition to heterotrophy (Madigan, 2005; Rodrigues-Diaz et al., 2008) and members of the Pseudonocardiaceae have demonstrated the ability to perform hydrogen sulfide oxidation as well as heterotrophy (Reichert et al., 1998; Chen et al., 2009). Because the harshest environmental conditions of the subnival zone are more common in remote portions of the landscape, it may be that these two extremophilic bacterial clades are early colonizers of recently exposed soils and later facilitate plant colonization via their potential to form symbioses or because they improve soil conditions. This phenomenon is similar to what is seen in the primary soils from pyrite weathering (Choler et al., 2001) and experimental work to tease apart the environmental versus biotic association is needed to further explore these patterns.

A caveat with this correlation network approach is that the correlation between a plant species and a bacterial clade may be the result of environmental factors shaping the distribution of both groups independently, a symbiotic/competitive/facilitative interaction, or even a tertiary relationship such as are seen with parasites of a parasite. However, that 75% of the clades to which we could assign hypothetical functions appear to have the potential to form symbioses with plants (six of eight, Table 1; Figure 3) suggests that we are identifying true plant-bacteria associations. It also suggests that the many of the strongly correlated Acidobacteria or TM7 clades, despite their unknown functional capacities, are associated with plants in this landscape.


We found evidence of three hypothesized assembly drivers between plant species and bulk soil bacteria using a correlational-based analysis along a gradient of environmental harshness in the subnival landscape of Niwot Ridge. First, our findings suggest that the abundance of bacteria-promoting plant species may serve as an indicator or even drive the patterns of plant-associated groups for specific ecosystem types within a landscape. Second, bacterial clades with putative plant symbiosis capacity, as inferred from the close relationship of sequences within a clade to known isolates, were not more likely to be correlated with plant species but have narrower phylogenetic breadth than putative plant-independent clades. Third, our analysis suggests that the influence of environmental harshness on plant-bacterial associations results in fewer plant-bacteria associations in harsh areas than in the less harsh, tundra proximal portion of the landscape. Our results provide the first description of plant-bacteria interactions at the species/clade level and demonstrate an overwhelming number of plant species specific associations with soil bacteria. In addition, facilitative associations appear to be more common than inhibitory associations in the subnival zone. One obvious next step is to test how often these bacteria are indeed found on or within the roots of the plants they co-occur with and if they affect plant growth or survival as opposed to co-occurring due to shared environmental preferences. If co-occurrence relationships are as important for the ecology of high-alpine systems as our correlation network suggests, then the biotic community’s functional resilience is likely sensitive to disturbances affecting either the plant or soil microbial community.

Conflict of Interest Statement

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.


This work was supported by the NSF Microbial Observatories Program (MCB-0455606). Logistical assistance was provided by the Niwot Ridge LTER site.

Supplementary Material

The Supplementary Material for this article can be found online at

Datasheet S1. Initial best AIC ranked models predicting bacterial clade relative abundance with plant species abundances.

Datasheet S2. Best AIC ranked models predicting harshness-upweighted bacterial clade relative abundance with plant species abundances.

Datasheet S3. Best AIC ranked models predicting harshness-downweighted bacterial clade relative abundance with plant species abundances.

Datasheet S4. A correlation matrix of plant species abundances and bacterial clade relative abundances (Pearson r values). A single * designates a correlation that is p-value < 0.01 for a two-tailed t-test of rho = 0; ** indicates p < 0.001; *** indicates p < 0.0001. The Bonferroni correction for alpha with 325 comparisons is p < 0.0002.

Datasheet S5. A combination of two correlation matrices (Pearson r values). The upper right triangle in bold represents correlations between bacterial clades and plant abundances with remote locations upweighted. The lower left triangle represents correlations between bacterial clades and plant abundances with remote locations down-weighted. A single * designates a correlation that is p-value < 0.01 for a two-tailed t-test of rho = 0; ** indicates p < 0.001; *** indicates p < 0.0001. The Bonferroni correction for alpha with 325 comparisons is p < 0.0002.


Ackerly, D. D. (2003). Community assembly, niche conservatism, and adaptive evolution in changing environments. Int. J. Plant Sci. 164, S165–S184.

CrossRef Full Text

Akaike, H. (1974). A new look at the statistical model identification. IEEE Trans. Automat. Contr. 19, 716–723.

CrossRef Full Text

Barberán, A., Bates, S. T., Casamayor, E. O., and Fierer, N. (2012). Using network analysis to explore cooccurrence patterns in soil microbial communities. ISME J. 6, 343–351.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Berg, G., and Smalla, K. (2009). Plant species and soil type cooperatively shape the structure and function of microbial communities in the rhizosphere. FEMS Microbiol. Ecol. 68, 1–13.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Bever, J. D., Dickie, I. A., Facelli, E., Facelli, J. M., Klironomos, J., Moora, M., Rillig, M. C., Stock, W. D., Tibbett, M., and Zobel, M. (2010). Rooting theories of plant community ecology in microbial interactions. Trends Ecol. Evol. (Amst.) 25, 468–478.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Bezemer, T. M., Fountain, M. T., Barea, J. M., Christensen, S., Dekker, S. C., Duyts, H., van Hal, R., Harvey, J. A., Hedlund, K., Maraun, M., Mikola, J., Mladenov, A. G., Robin, C., de Ruiter, P. C., Scheu, S., Setala, H., Smilaure, P., and van der Puttern, W. H. (2010). Divergent composition but similar function of soil food webs of individual plants: plant species and community effects. Ecology 91, 3027–3036.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Bianciotto, V., Minerdi, D., Perotto, S., Bonfante, P., and Vegetale, B. (1996). Cellular interactions between arbuscular mycorrhizal fungi and rhizosphere bacteria. Protoplasma 193, 23–131.

CrossRef Full Text

Bonfante, P., and Anca, I. A. (2009). Plants, mycorrhizal fungi, and bacteria: a network of interactions. Annu. Rev. Microbiol. 63, 363–383.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Bonferroni, C. E. (1936). Teoria statistica delle classi e calcolo delle probabilit ‘a. Pubblicazioni del R Istituto Superiore di Scienze Economiche e Commerciali di Firenze 8, 3–62.

Bowman, W. D., Steltzer, H., Rosenstiel, T. N., Cleveland, C. C., and Meier, C. L. (2004). Litter effects of two co-occurring alpine species on plant growth, microbial activity and immobilization of nitrogen. Oikos 140, 336–344.

CrossRef Full Text

Brenner, D. J., Krieg, N. R., and Staley, J. T. (2005). Bergey’s Manual of Systematic Bacteriology. Vol. Two, Part C, The Alpha-, Beta-, Delta-, and Epsilonproteobacteria, 2nd Edn. New York: Springer.

Bruno, J. F., Stachowicz, J. J., and Bertness, M. D. (2003). Inclusion of facilitation into ecological theory. Trends Ecol. Evol. (Amst.) 18, 119–125.

CrossRef Full Text

Buckley, D. H., Huangyutitham, V., Hsu, S., and Nelson, T. A. (2007). Stable isotope probing with 15N2 reveals noncultivated diazotroph in soil. Appl. Environ. Microbiol. 73, 3196–3204.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Callaway, R. M., and Walker, L. R. (1997). Competition and facilitation: a synthetic approach to interactions in plant communities. Ecology 78, 1958–1965.

CrossRef Full Text

Caporaso, J. G., Paszkiewicz, K., Field, D., Knight, R., and Gilbert, J. A. (2011). The Western English Channel contains a persistent microbial seed bank. ISME J. doi:10.1038/ismej.2011.162

CrossRef Full Text

Carlson, M. L., Flagstad, L. A., Gillet, F., and Mitchell, E. A. D. (2012). Community development along a proglacial chronosequence: are above-ground and below-ground community structure controlled more by biotic than abiotic factors? J. Ecol. 98, 1084–1095.

CrossRef Full Text

Carvalho, F. M., Souza, R. C., Barcellos, F. G., Hungria, M., and Vasconcelos, A. T. (2010). Genomic and evolutionary comparisons of diazotrophic and pathogenic bacteria of the order Rhizobiales. BMC Microbiol. 10, 37. doi: 10.1186/1471-2180-10-37

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Cazares, E., Trappe, J. M., and Jumpponen, A. (2005). Mycorrhiza-plant colonization patterns on a subalpine glacier forefront as a model system of primary succession. Mycorrhiza 15, 405–416.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Chapin, F. S., Walker, L. R., Fastie, C. L., and Sharman, L. C. (1994). Mechanisms of primary succession following deglaciation at Glacier Bay, Alaska. Ecol. Monogr. 64, 149–175.

CrossRef Full Text

Chase, J. M., and Leibold, M. A. (2003). Ecological Niches: Linking Classical and Contemporary Approaches. Chicago, IL: University of Chicago Press.

Chen, H., Qin, S., Li, J., Zhang, Y., Xu, L., Jiang, C., Kim, C., and Li, W. (2009). Pseudonocardia endophytica sp. nov., isolated from the pharmaceutical plant Lobelia clavata. Int. J. Syst. Evol. Microbiol. 59, 559–563.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Choler, P., Michalet, R., and Callaway, R. M. (2001). Facilitation and competition on gradients in alpine plant communities. Ecology 82, 3295–3308.

CrossRef Full Text

Compant, S., Duffy, B., Nowak, J., Clement, C., and Barka, E. A. (2005). Use of plant growth-promoting bacteria for biocontrol of plant diseases: principles, mechanisms of action, and future prospects. Appl. Environ. Microbiol. 71, 4951–4959.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Compant, S., Nowak, J., Coeneye, T., Clement, C., and Barka, A. B. (2008). Diversity and occurrence of Burkholderia spp. in the natural environment. FEMS Microbiol. Rev. 32, 607–626.

CrossRef Full Text

Cox, T. F., and Cox, M. A. A. (1994). Multidimensional Scaling. London: Chapman & Hall.

DeSantis, T. Z., Hugenholtz, P., Larsen, N., Rojas, M., Brodie, E. L., Keller, K., Huber, T., Dalevi, D., Hu, P., and Andersen, G. L. (2006). Greengenes, a Chimera-Checked 16S rRNA gene database and workbench compatible with ARB. Appl. Environ. Microbiol. 72, 5069–5072.

Diamond, J. M. (1975). “Assembly of species communities,” in Ecology and Evolution of Communities, eds M. L. Cody and J. M. Diamond (Cambridge, MA: Harvard University Press), 342–444.

Diaz, S., Cabido, M., and Casanoves, F. (1998). Plant functional traits and environmental filters at a regional scale. J. Veg. Sci. 9, 113–122.

CrossRef Full Text

Erickson, T. A., Williams, M. W., and Winstral, A. (2005). Persistence of topographic controls on the spatial distribution of snow in rugged mountain terrain, Colorado, United States. Water Resour. Res. 41, W04014. doi:10.1029/2003WR002973

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Eskelinen, A., Stark, S., and Männistö, M. (2009). Links between plant community composition, soil organic matter quality and microbial communities in contrasting tundra habitats. Oecologia 161, 113–123.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Fierer, N., Hamady, M., Lauber, C. L., and Knight, R. (2008). The influence of sex, handedness, and washing on the diversity of hand surface bacteria. Proc. Natl. Acad. Sci. U.S.A. 105, 17994–17999.

CrossRef Full Text

Fisk, M. C., and Schmidt, S. K. (1995). Nitrogen mineralization and microbial biomass nitrogen dynamics in three alpine tundra communities. Soil Sci. Soc. Am. J. 59, 1036–1043.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Freeman, K. R., Pescador, M. Y., Reed, S. C., Costello, E. K., Robeson, M. S., and Schmidt, S. K. (2009). Soil CO2 flux and photoautotrophic community composition in high-elevation, “barren” soil. Environ. Microbiol. 11, 674–686.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Freilich, S., Kreimer, A., Meilijson, I., Gophna, U., Sharan, R., and Ruppin, E. (2010). The large-scale organization of the bacterial network of ecological cooccurrence interactions. Nucleic Acids Res. 38, 3857–3868.

CrossRef Full Text

Fuhrman, J. A., and Steele, J. A. (2008). Community structure of marine bacterioplankton: patterns, networks, and relationships to function. Aquat. Microb. Ecol. 53, 69–81.

Gonzalez, A., King, A., Robeson Ii, M. S., Song, S., Shade, A., Metcalf, J. L., and Knight, R. (2011). Characterizing microbial communities through space and time. Curr. Opin. Biotechnol. 24, 431–436.

CrossRef Full Text

Graff, A., and Conrad, R. (2006). Impact of flooding on soil bacterial communities associated with poplar (Populus sp.) trees. FEMS Microbiol. Ecol. 53, 401–415.

CrossRef Full Text

Grime, J. P. (1998). Benefits of plant diversity to ecosystems: immediate, filter and founder effects. J. Ecol. 86, 902–910.

CrossRef Full Text

Grytnes, J. A. (2000). Fine-scale vascular plant species richness in different alpine vegetation types: relationships with biomass and cover. J. Veg. Sci. 11, 87–92.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Haichar, F. Z., Marol, C., Berge, O., Rangel-Castro, J. I., Prosser, J. I., Balesdent, J., Heulin, T., and Achouak, W. (2008). Plant host habitat and root exudates shape soil bacterial community structure. ISME J. 2, 1221–1230.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Hamady, M., Lozupone, C., and Knight, R. (2010). Fast unifrac: facilitating high-throughput phylogenetic analyses of microbial communities including analysis of pyrosequencing and phylochip data. ISME J. 4, 17–27.

Harvey, P. H., and Pagel, M. D. (1991). The Comparative Method in Evolutionary Biology. Oxford: Oxford University Press.

Hayat, R., Ali, S., Amara, U., Khalid, R., and Ahmed, I. (2010). Soil beneficial bacteria and their role in plant growth promotion: a review. Ann. Microbiol. 60, 579–598.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Hobbie, E. A., Jumpponen, A., and Trappe, J. (2005). Foliar and fungal 15N:14N ratios reflect development of mycorrhizae and nitrogen supply during primary succession: testing analytical models. Oecologia 146, 258–268.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Horner-Devine, M. C., Silver, J., Bohannan, B. J. M., Colwell, R. K., Fuhrman, J. A., Green, J. L., Kuske, C. R., Martiny, J. B. H., Muyzer, G., Naeem, S., Øvreås, L., Reysenbach, A.-L., and Smith, V. H. (2007). A comparison of taxon co-occurrence patterns for macro- and microorganisms. Ecology 88, 1345–1353.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

King, A. J., Freeman, K. R., McCormick, K. F., Lynch, R. C., Lozupone, C., Knight, R., and Schmidt, S. K. (2010). Biogeography and habitat modelling of high-alpine bacteria. Nat. Commun. 1, 53.

CrossRef Full Text

King, A. J., Meyer, A. F., and Schmidt, S. K. (2008). High levels of microbial biomass and activity in unvegetated tropic and temperate alpine soils. Soil Biol. Biochem. 40, 2605–2610.

CrossRef Full Text

Knelman, J. E., Legg, T. M., O’Neill, S. P., Washenberger, C. L., González, A., Cleveland, C. C., and Nemergut, D. R. (2012). Bacterial community structure and function change in association with colonizer plants during early primary succession in a glacier forefield. Soil Biol. Biochem. 46, 172–180.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Körner, C. (2007). The use of “altitude” in ecological research. Trends Ecol. Evol. (Amst.) 22, 569–574.

CrossRef Full Text

Kremer, R. J. (2006). “Deleterious rhizobacteria,” in Plant-Associated Bacteria, ed. S. Gnanamanickam (Dordrecht: Springer), 335–357.

Lee, M. S., Do, J. O., Park, M. S., Jung, S., Lee, K. H., Bae, K. S., Park, S. J., and Kim, S. B. (2006). Dominance of Lysobacter sp. in the rhizosphere of two coastal sand dune plant species, Calystegia soldanella and Elymus mollis. Antonie van Leeuwenhoek 90, 19–27.

CrossRef Full Text

Ley, R. E., Williams, M. W., and Schmidt, S. K. (2004). Microbial population dynamics in an extreme environment: controlling factors in talus soils at 3750 m in the Colorado Rocky Mountains. Biogeochemistry 68, 313–335.

CrossRef Full Text

Li, J., and Kremer, R. J. (2006). Growth response of weed and crop seedlings to deleterious rhizobacteria. Biol. Contr. 39, 58–65.

CrossRef Full Text

Lipson, D. A., Schadt, C. W., Schmidt, S. K., and Monson, R. K. (2002). Ectomycorrhizal transfer of amino acid-nitrogen to the alpine sedge Kobresia myosuroides. New Phytologist 142, 163–167.

CrossRef Full Text

Litaor, M. I., Williams, M., and Seastedt, T. R. (2008). Topographic controls on snow distribution, soil moisture, and species diversity of herbaceous alpine vegetation, Niwot Ridge, Colorado. J. Geophys. Res. 113, G02008. doi:10.1029/2007JG000419

CrossRef Full Text

MacArthur, R., and Wilson, E. (1967). The Theory of Island Biogeography. Princeton, NJ: Princeton University Press.

Madigan, M. T. (2005). Anoxygenic phototrophic bacteria from extreme environments. Discov. Photosynth. 20, 969–983.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Mahaffee, W. F., and Kloepper, J. W. (1997). Temporal changes in the bacterial communities of soil, rhizosphere, and endorhiza associated with field-grown cucumber (Cucumis sativus L.). Microb. Ecol. 34, 210–223.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Marcy, Y., Ouverney, C., Bik, E. M., Lösekann, T., Ivanova, N., Martin, H. G., Szeto, E., Platt, D., Hugenholtz, P., Relman, D. A., and Quake, S. R. (2007). Dissecting biological “dark matter” with single-cell genetic analysis of rare and uncultivated TM7 microbes from the human mouth. Proc. Natl. Acad. Sci. U.S.A. 104, 11889–11894.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Márquez, L. M., Redman, R. S., Rodriguez, R. J., and Roossinck, M. J. (2007). A virus in a fungus in a plant – three way symbiosis required for thermal tolerance. Science 315, 513–515.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Martiny, J. B., Bohannan, B. J. M., Brown, J. H., Colwell, R., Fuhrman, J., Green, J., Horner-Devine, M., Kane, M., Krumins, J., Kuske, C., Morin, P., Naeem, S., Ovreas, L., Reysenbach, A., Smith, V., and Staley, J. (2006). Microbial biogeography: putting microorganisms on the map. Nat. Rev. Microbiol. 4, 102–112.

McCune, B., Grace, J. B., and Urban, D. L. (2002). Analysis of Ecological Communities. Oregon: MjM Software Design.

Mullen, R. B., Schmidt, S. K., and Jaeger, C. H. (1998). Nitrogen uptake during snowmelt by the snow buttercup, Ranunculus adoneus. Arct. Antarct. Alp. Res. 30, 121–125.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Nemergut, D. R., Anderson, S. P., Cleveland, C. C., Martin, A. P., Miller, A. E., Seimon, A., and Schmidt, S. K. (2007). Microbial community succession in an unvegetated, recently deglaciated soil. Microb. Ecol. 53, 110–122.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Nemergut, D. R., Costello, E. K., Meyer, A. F., Pescador, M. Y., Weintraub, M. N., and Schmidt, S. K. (2005). Structure and function of Alpine and Arctic soil microbial communities. Res. Microbiol. 156, 775–784.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Norris, P. R., Davis-Belmar, C. S., Brown, C. F., and Calvo-Bado, L. A. (2011). Autotrophic, sulfur-oxidizing actinobacteria in acidic environments. Extremophiles 15, 155–163.

Oksanen, J., Blanchet, F. G., Kindt, R., Legendre, P., O’Hara, R. B., Simpson, G. L., Solymos, P., Stevens, M. H. H., and Wagner, H. (2010). vegan: Community Ecology Package. R package version 1.17–13.

CrossRef Full Text

Olofsson, J., Ericson, L., Torp, M., Stark, S., and Baxter, R. (2011). Carbon balance of Arctic tundra under increased snow cover mediated by a plant pathogen. Nat. Clim. Chang. 1, 220–223.

CrossRef Full Text

Qin, S., Chen, H., Zhao, G., Li, J., Zhu, W., Xu, L., Jiang, J., and Li, W. (2012). Abundant and diverse endophytic Actinobacteria associated with medicinal plant Maytenus austroyunnanensis in Xishuangbanna tropical rainforest revealed by culture-dependent and culture-independent methods. Environ. Microbiol. Rep. doi:10.1111/j.1758-2229.2012.00357.x

CrossRef Full Text

R Development Core Team. (2011). R: A Language and Environment for Statistical Computing. Vienna: R Foundation for Statistical Computing.

Reichert, K., Lipski, A., Pradella, S., Stakebrandt, E., and Altendorf, K. (1998). Pseudonocardia asaccharolytica sp. nov. and Pseudonocardia sulfidoxydans sp. nov., two new dimethyl disulfide-degrading actinomycetes and emended description of the genus Pseudonocardia. Int. J. Syst. Evol. Microbiol. 48, 441–449.

CrossRef Full Text

Reynolds, H. L., Packer, A., Bever, J. D., and Clay, K. (2003). Grassroots ecology: plant-microbe-soil interactions as drivers of plant community structure and dynamics. Ecology 84, 2281–2291.

Rodrigues-Diaz, M., Rodelas-Gonzales, B., Pozo-Clemente, C., Martinez-Toled, M. V., and Gonzalez-Lopez, J. (2008). “A review on the taxonomy and possible screening traits of plant growth promoting rhizobacteria,” in Plant-Bacteria Interactions: Strategies and Techniques to Promote Plant Growth, Chap. 4, eds I. Ahmad, J. Pichtel, and S. Hayat (Weinheim: Whiley-VCH), 55–80.

Ruan, Q., Dutta, D., Schwalbach, M. S., Steele, J. A., Fuhrman, J. A., and Sun, F. (2006). Local similarity analysis reveals unique associations among marine bacterioplankton species and environmental factors. Bioinformatics 22, 2532.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Rudgers, J. A., Miller, T. E. X., Ziegler, S. M., and Craven, K. D. (2012). There are many ways to be a mutualist: endophytic fungus reduces plant survival but increases population growth. Ecology 93, 565–574.

CrossRef Full Text

Schmidt, S. K., Kageyama, S. A., Halloy, S. R. P., and Schadt, C. W. (2008a). Mycorrhizal and dark-septate fungi in plant roots above 4270 meters elevation in the Andes and Rocky mountains. Arct. Antarct. Alp. Res. 40, 576–583.

CrossRef Full Text

Schmidt, S. K., Reed, S. C., Nemergut, D. R., Grandy, A. S., Cleveland, C. C., Costello, E. K., Weintraub, M. N., Martin, A. P., and Neff, J. C. (2008b). The earliest stages of ecosystem succession in high-elevation (5000 m.a.s.l.), recently de-glaciated soils. Philos. Trans. R. Soc. Lond. B Biol. Sci. 275, 2793–2802.

CrossRef Full Text

Seastedt, T. R., and Vaccaro, L. (2001). Plant species richness, productivity, and nitrogen and phosphorus limitations across a snowpack gradient in alpine tundra, Colorado, U.S.A. Arct. Antarct. Alp. Res. 33, 100–106.

CrossRef Full Text

Seeds, J. D., and Bishop, J. G. (2009). Low Frankia inoculation potentials in primary successional sites at Mount St. Helens, Washington, USA. Plant Soil 323, 225–233.

CrossRef Full Text

Sheng, H. M., Gao, H. S., Xue, L. G., Ding, S., Song, C. L., Feng, H. Y., and An, L. Z. (2010). Analysis of the composition and characteristics of culturable Endophytic bacteria within subnival plants of the Tianshan mountains, Northwestern China. Curr. Microbiol. 62, 923–932.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Stafford, W. H. L., Baker, G. C., Brown, S. A., Burton, S. G., and Cowan, D. A. (2005). Bacterial diversity in the rhizosphere of Proteaceae species. Environ. Microbiol. 7, 1755–1768.

CrossRef Full Text

Tscherko, D., Hammesfahr, U., Zeltner, G., Kandeler, E., and Böcker, R. (2005). Plant succession and rhizosphere microbial communities in a recently deglaciated alpine terrain. Basic Appl. Ecol. 6, 367–383.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

van der Heijden, M. G. A., Bardgett, R. D., and Straalen, N. M. V. (2008). The unseen majority: soil microbes as drivers of plant diversity and productivity in terrestrial ecosystems. Ecol. Lett. 11, 296–310.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Vile, D., Shipely, B., and Garnier, E. (2006). Ecosystem productivity can be predicted from potential relative growth rate and species abundance. Ecol. Lett. 9, 1061–1067.

CrossRef Full Text

Walker, L. R., and del Moral, R. (2003). Primary Succession and Ecosystem Rehabilitation. Cambridge: Cambridge University Press.

Wang, B., and Qiu, Y.-L. (2006). Phylogenetic distribution and evolution of mycorrhizas in land plants. Mycorrhiza 16, 299–363.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Wang, Q., Garrity, G. M., Tiedje, J. M., and Cole, J. R. (2007). Naïve Bayesian classifier for rapid assignment of rRNA sequences into the new bacterial taxonomy. Appl. Environ. Microbiol. 73, 5261–5267.

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Webber, C. F., and King, G. M. (2010). Distribution and diversity of carbon monoxide-oxidizing bacteria and bulk bacterial communities across a succession gradient on a Hawaiian volcanic deposit. Environ. Microbiol. 12, 1855–1867.

Webber, W. A., and Whittmann, R. C. (2001). Colorado Flora: Eastern Slope, 3rd Edn. Boulder, CO: University Press of Colorado.

Weiher, E., and Keddy, P. A. (1995). The assembly of experimental wetland plant communities. Oikos 73, 323–335.

CrossRef Full Text

Zinger, L., Lejon, D. P. H., Baptist, F., Bouasria, A., Aubert, S., Geremia, R. a., and Choler, P. (2011). Contrasting diversity patterns of crenarchaeal, bacterial and fungal soil communities in an alpine landscape. PLoS ONE 6, e19950. doi:10.1371/journal.pone.0019950

CrossRef Full Text

Keywords: community assembly, co-occurrence networks, facilitation, mutualism, Niwot Ridge, plant-microbe interactions, soil microbial communities, symbiosis

Citation: King AJ, Farrer EC, Suding KN and Schmidt SK (2012) Co-occurrence patterns of plants and soil bacteria in the high-alpine subnival zone track environmental harshness. Front. Microbio. 3:347. doi: 10.3389/fmicb.2012.00347

Received: 15 June 2012; Accepted: 08 September 2012;
Published online: 11 October 2012.

Edited by:

Ashley Shade, Yale University, USA

Reviewed by:

Michael S. Strickland, Yale University, USA
Lucie Zinger, Centre National de la Recherche Scientifique, France

Copyright: © 2012 King, Farrer, Suding and Schmidt. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in other forums, provided the original authors and source are credited and subject to any copyright notices concerning any third-party graphics etc.

*Correspondence: Andrew J. King, Ecosystem Sciences, Commonwealth Scientific and Industrial Research Organisation, Clunies Ross Street, Acton, ACT 2601, Australia. e-mail: