Abstract
- Top of page
- Abstract
- Introduction
- Materials and methods
- Results
- Discussion
- Acknowledgements
- References
- Supporting Information
Non-native, invasive grasses have been linked to altered grass-fire cycles worldwide. Although a few studies have quantified resulting changes in fire activity at local scales, and many have speculated about larger scales, regional alterations to fire regimes remain poorly documented. We assessed the influence of large-scale Bromus tectorum (hereafter cheatgrass) invasion on fire size, duration, spread rate, and interannual variability in comparison to other prominent land cover classes across the Great Basin, USA. We compared regional land cover maps to burned area measured using the Moderate Resolution Imaging Spectroradiometer (MODIS) for 2000–2009 and to fire extents recorded by the USGS registry of fires from 1980 to 2009. Cheatgrass dominates at least 6% of the central Great Basin (650 000 km2). MODIS records show that 13% of these cheatgrass-dominated lands burned, resulting in a fire return interval of 78 years for any given location within cheatgrass. This proportion was more than double the amount burned across all other vegetation types (range: 0.5–6% burned). During the 1990s, this difference was even more extreme, with cheatgrass burning nearly four times more frequently than any native vegetation type (16% of cheatgrass burned compared to 1–5% of native vegetation). Cheatgrass was also disproportionately represented in the largest fires, comprising 24% of the land area of the 50 largest fires recorded by MODIS during the 2000s. Furthermore, multi-date fires that burned across multiple vegetation types were significantly more likely to have started in cheatgrass. Finally, cheatgrass fires showed a strong interannual response to wet years, a trend only weakly observed in native vegetation types. These results demonstrate that cheatgrass invasion has substantially altered the regional fire regime. Although this result has been suspected by managers for decades, this study is the first to document recent cheatgrass-driven fire regimes at a regional scale.
Introduction
- Top of page
- Abstract
- Introduction
- Materials and methods
- Results
- Discussion
- Acknowledgements
- References
- Supporting Information
One of the most notorious ecosystem consequences of non-native plant invasions is the alteration of fire regimes (D'Antonio & Vitousek, 1992; Brooks et al., 2004). Increased fire occurrence, intensity, and severity has been observed in association with invasion by buffelgrass in the US southwest and Mexico (Burquez-Montijo et al., 2002) and Australia (Butler & Fairfax, 2003), gamba grass in Australia (Setterfield et al., 2010), Molasses grass and broomsedge in Hawai'i (Tunison et al., 2001), and cogongrass in the US southeast (Lippincott, 2000). This ‘grass-fire’ cycle is driven by higher fine fuel biomass, increased flammability of grasses and/or faster postfire recovery of non-native grasses compared to native species. This phenomenon has been identified globally (Balch et al., 2009; Bowman et al., 2009), but is pronounced in semiarid ecosystems with historically low fire occurrence (D'Antonio & Vitousek, 1992; Brooks et al., 2004). One of the most widely cited examples of a novel grass-fire cycle is the fire activity that has followed cheatgrass (Bromus tectorum) invasion into the US Great Basin (Mack, 1981; Whisenant, 1990; Knapp, 1996). On the basis of the fire history of 12 sites in southern Idaho, Whisenant (1990) estimated a fire return interval (FRI) of 3–5 years in cheatgrass-dominated rangelands, compared with 60–100 years in native sagebrush (Artemisia spp.). Beyond this study, it is not known how fire regimes have changed across the current extent of cheatgrass dominance – currently estimated at over 40 000 km2 (Bradley & Mustard, 2008) – within 650 000 km2 of land area in the Great Basin.
Invasive grasses that alter the fire cycle are known to increase fire size, fire season length, spread rate, numbers of individual fires and likelihood of fires spreading into surrounding native or managed ecosystems (D'Antonio & Vitousek, 1992; Brooks et al., 2004). However, with the exception of fire size (Knapp et al., 1998), these relationships have yet to be evaluated for cheatgrass at a regional scale. Cheatgrass could change the properties of fire regimes through a number of mechanisms. It increases fine fuel continuity (Whisenant, 1990), enabling fire spread (Link et al., 2006). It also increases fine fuel biomass, particularly following wet years (Hull & Pechanec, 1947; Bradley & Mustard, 2005), and may alter micrometeorological conditions, decreasing surface soil moisture and raising soil temperatures relative to shrublands due to its shallow root system (Prater et al., 2006).
Furthermore, the mechanisms by which cheatgrass alters fire regimes likely interact with climate. For example, cheatgrass cover and biomass vary with climate (Chambers et al., 2007) and are promoted by wet and warm conditions during the fall and spring (Knapp, 1998). Interannual variability in precipitation driven by El Niño cycles creates years with extremely high cheatgrass biomass (Hull & Pechanec, 1947; Bradley & Mustard, 2005) and others with almost none. In native shrub and grassland ecosystems of the arid western United States, high antecedent precipitation has been shown to be one of the strongest predictors of government-registered burned area (1977–2003), even more so than current-year temperature or drought conditions (Littell et al., 2009). The oscillation between wet years that enable substantial grass growth and dry years that desiccate those built-up fuels may create ideal conditions for high fire years, but this hypothesis remains untested for cheatgrass rangelands. Moreover, drier conditions may also make resident shrubs more flammable, particularly if drier than normal conditions follow a wet year where shrub growth was high. Therefore, the coupling of a wet year and a ‘drier than normal’ year could provide the right climatic oscillation to promote cheatgrass and fires.
The US Great Basin covers over 650 000 km2 and supports a large number of endemic species (Kier et al., 2009). Historically, fire has been a rare event in low and mid elevation Great Basin ecosystems and many of the native plant species are not fire-tolerant (Riegel et al., 2006). The loss of native-dominated shrubland ecosystems has been linked to the decline of sagebrush-dependent species such as the Greater Sage grouse, currently being considered for listing as an endangered species (Crawford et al., 2004; Connelly et al., 2011). In addition, fire driven conversion of shrubland to grassland has been linked to a loss of carbon storage (Bradley et al., 2006; Prater et al., 2006) and available soil water (Obrist et al., 2003; Prater et al., 2006). Cheatgrass-facilitated fire also presents challenges to human populations and agency budgets in the region. The urban wildland interface in the region has grown dramatically (Theobald & Romme, 2007), and the result is millions of dollars in budgeted and unbudgeted expenses related to fire suppression, fuels management, emergency activities, and postfire rehabilitation (Roberts, 1999; Calkin et al., 2005).
Although the introduced grass-fire cycle and its ecological impacts are recognized (D'Antonio & Vitousek, 1992; Brooks et al., 2004), accurate forecasting of fire risk in the Great Basin requires better understanding of how cheatgrass currently alters fire regimes and the interactions between grass-fueled fire and climate. Cheatgrass has not only invaded many ecosystems of the US Great Basin – predominantly big sagebrush (Artemisia tridentata) ecosystems (Chambers et al., 2007) but also pinyon-juniper (Barney & Frischknecht, 1974), and to a lesser extent salt desert shrublands (Haubensak et al., 2009). It is more limited in its establishment >1600 m (Sherrill & Romme, 2012), such as in the higher elevations of the pinyon-juniper zone and subalpine shrubland, montane meadows, and the most saline areas of the valley bottoms (alkali flats). In big sagebrush ecosystems, reported FRIs range from 13 to 25 years (Frost 1998) to 150 years (Baker, 2006; Riegel et al., 2006). In pinyon-juniper, fire returns are estimated ~50 years (Riegel et al., 2006) and as high as 200 years (Schmidt et al., 2002). In the lower, hotter desert shrubland ecosystems sometimes called ‘salt desert’ and typically dominated by salt tolerant species in the Chenopodiaceae (hereafter desert shrubland), less is known about the fire return and fire-sensitivity of these drought- and high salinity-adapted species (Haubensak et al., 2009).
Our overarching prediction is that cheatgrass would increase fire likelihood due to more continuous, drier, and higher fine fuel loads, relative to the shrublands and forests that it has replaced. These fuels will result in both increased fire ignition probability and increased spread. Here, we use Moderate Resolution Imaging Spectroradiometer (MODIS) satellite-based burned area (2000–2009) data and the USGS registry of fire incidents (1980–2009), to determine whether or not cheatgrass increases fire activity across the US Great Basin. Compared with other vegetation types, including montane shrubland, sagebrush steppe, pinyon-juniper, desert shrubland, and agriculture, we document whether or not cheatgrass-dominated areas: (i) have higher fire frequency (i.e., lower FRI), (ii) larger average fire size and faster fire spread rates, (iii) are more likely to be ignition points for fire spread, and (iv) show shifts in the seasonality and interannual variability in fires.