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Editors' Call ARTICLES High Altitude Wetland Mitigation on the Uncompahgre Plateau Handbook for Developing Watershed Plans Salt or Saltcedar The American Beaver Upper Arkansas River Basin FEATURES Legal Developments Message from the President Research Summaries BACK ISSUES Volume 18, Number 3 Winter 2007/2008 Volume 18, Number 2 Summer/Fall 2007 Volume 18, Number 1 Spring 2007 Index of Back Issues |
Which came first, the salt or the saltcedar?A quantitative study of soil and groundwater chemistry along the Middle Rio Grande, New Mexicoby Michelle Cederborg, Ph.D. Candidate, University of Denver, Colorado
As the common name "saltcedar" implies, one of the most often cited mechanisms of ecosystem change by this species stems from its ability to sequester salts in its tissues (Thomson et al. 1969). This deciduous tree can extract salts from the groundwater, excrete these compounds through leaf tissue, and deposit them onto the soil surface through mature leaf senescence and exudation (Ladenburger et al. 2006, Lesica and DeLuca 2004, Shafroth et al. 1995). This alteration of surface salt concentrations has the ability to disrupt soil nutrient dynamics and contaminate surface waters with potential negative consequences for local plant and animal populations. Knowledge of invasion mechanisms and long-term environmental impacts of saltcedar is fundamental for understanding habitat restoration and revegetation potential upon its removal. Excess soluble salts, typically dominated by sodium compounds, begin to become troublesome for plant species when they accumulate in soils. Under high concentrations of sodium, elements such as calcium and magnesium are often lost from the system leaving soils deficient in these plant-essential nutrients. In addition, the forces that bind clay particles together are disrupted when too many large sodium ions are present. When this separation occurs, the clay particles expand, causing swelling and soil dispersion. Soil dispersion leads to reduced water infiltration which can result in reduced plant-available water and increased runoff and soil erosion. The outcome becomes even more dismal for plants without a mechanism for compartmentalizing salts within their tissues. Unlike saltcedar, most native riparian species do not possess salt glands (structures that serve to sequester and dispose of ingested salts without harm to the plant's internal structure and function). Native riparian plants must therefore regulate their salt uptake at the root-soil interface which can lead to a build-up of excess salts outside of plant roots. As salt concentrations rise above that of the plant's internal environment, the osmotic potential of the soil decreases and plants become less able to extract water from the soil. Even with access to an abundant water source the plant suffers from drought stress, a condition that becomes more severe with increased salinity. Elevated salt concentrations are well documented to negatively impact establishment and growth of native riparian species such as cottonwood and willow (Glenn et al. 1998, Rowland et al. 2004, Vandersande et al. 2001) and salt-cedar has even been labeled allelopathic via this mechanism of salt retranslocation (Brock 1994, Brotherson and Field 1987). No quantitative support of this assumption in the context of environmental factors that may also influence surface salt levels, however, currently exists in the published literature. Environmental factors such as geology, climate, and anthropogenic practices could predispose an area to elevated salt levels. Areas where groundwater comes in contact with volcanic vents that transport magnesium and sodium ions from the earth's mantle and sites where the rock types contain high concentrations of rapidly weathered salt constituents tend to have higher levels of environmental salinity. In addition, soil salinity is typically exacerbated in arid regions due to a lack of sufficient rainfall that would leach and transport salt deposits, and high evaporation rates; such factors tend to further concentrate salts in the surface soils. The most often cited cause of elevated salt concentrations along streams and rivers is river regulation (Busch and Smith 1995, Stromberg 2001). Flow-regulated and channelized river stretches can develop saline bankside conditions because they are no longer subject to periodic overbank flooding which washes salts from the soil. Since saltcedar is a facultative halophyte and can therefore tolerate and even thrive in conditions of elevated salinity (Glenn et al. 1998), it is questionable whether invasion of this opportunist is the cause or the effect of solute imbalances. In order to accurately charge saltcedar with environmental salt-loading, we need to take into account other potential sources contributing to elevated salt concentrations. Specifically, we need to know which came first, the salt or the saltcedar.
We chose to examine the relationship between saltcedar presence and elevated surface salinity within saltcedar-infested and native-dominated sites along a system that receives salt inputs from all of the fore mentioned sources, the Middle Rio Grande in central New Mexico. We selected saltcedar stands across a gradient of aboveground saltcedar ages (five to 40 years of age) and densities (native-dominated to complete saltcedar cover) to determine how these stand attributes relate to surface salt-loading. In addition, we chose stands in the proximal, active floodplain (exposed to annual flood events) and in the more distal, upper floodplain terraces (typically outside of the levees and deprived of overbank flooding) to hopefully isolate potential saltcedar-induced alterations to soils and surface water quality as well as address hydrologic impacts on environmental salinity. Preliminary data collected in 2006 show a strong relationship between surface soil salinity and flooding (Figure 2a). Areas sampled outside the active floodplain have significantly higher salt levels when compared with areas exposed to periodic flooding. These results would suggest that flooding is a dominant factor responsible for elevated salt concentrations along this river system. Our preliminary findings also show that areas with greater saltcedar densities have higher soil salt levels than areas with reduced saltcedar cover (Figure 2b). Similarly, we observed that areas dominated by saltcedar within the active floodplain contained higher levels of surface soil salts when compared with adjacent native-dominated sites. These results support the claim that saltcedar is actively contributing salts to the soil surface even in the presence of flooding. Preliminary results also suggest that beyond a certain age of saltcedar, surface soil salinity begins to decrease (Figure 3). This finding is contrary to what would be expected in an environment that has been subjected to repeated salt inputs for longer periods. Decadent saltcedar growth, however, tends to consist primarily of older woody material and has lower leaf area indices than younger saltcedar stands. The reduced saltcedar leaf area in older infestations likely leads to less salt redistribution to the soil surface through leaf material. In addition, the dense aboveground woody network associated with older growth may reduce solar radiation and elevate localized humidity levels at the soil surface; both of which can contribute to reduced capillary rise of salts to surface soils in arid regions. The extent to which saltcedar invasion alters soil chemistry has often been assumed to be large, but this claim is largely unverified. We collected over one thousand surface soils and groundwater samples in 2007 to better assess the role of saltcedar versus other factors (i.e. hydrology) in determining floodplain salinity. Soils and groundwater analyses will be directly compared to detailed vegetation surveys to determine how surface soil and groundwater salinity relate to species composition, density, and in the case of saltcedar, average individual age. At this time, it is assumed that decadent saltcedar stands may have already altered the soil to such a degree that any attempt at restoration would be futile. A complete analysis of this larger dataset will allow us to determine if this is indeed the case, or if, as preliminary data suggest, these older stands may actually have the least saline soils and are therefore more conducive to native riparian species revegetation. Literature Cited: Brotherson J. D. and D. Field. 1987. Tamarix: Impacts of a successful weed. Rangelands 9:110-112. Busch D. E. and S. D. Smith. 1995. Mechanisms associated with decline of woody species in riparian ecosystems of the southwestern U.S. Ecological Monographs 65:347-370. Glenn E., R. Tanner, S. Mendez, T. Kehret, D. Moore, J. Garcia, and C. Valdes. 1998. Growth rates, salt tolerance and water use characteristics of native and invasive riparian plants from the delta of the Colorado River, Mexico. Journal of Arid Environments 40:281-294. Ladenburger C.G., A.L. Hild, D.J. Kazmer, and L.C. Munn. 2006. Soil salinity patterns in Tamarix invasions in the Bighorn Basin, Wyoming, USA. Journal of Arid Environments 65:111-128. Lesica P. and T.H. DeLuca. 2004. Is tamarisk allelopathic? Plant and Soil 267:357-365. Rowland D. L., A. A. Sher, and D. L. Marshall. 2004. Inter- and Intra-population variation in seedling performance of Rio Grande cottonwood under low and high salinity. Canadian Journal of Forest Research 34:1458-1466. Shafroth P. B., J. M. Friedman, and L. S. Ischinger. 1995. Effects of salinity on establishment of Populus fremontii (cottonwood) and Tamarix ramosissima (saltcedar) in southwestern United States. Great Basin Naturalist 55:58-65. Sher A. A., D. L. Marshall, and J. P. Taylor. 2002. Establishment patterns of native Populus and Salix in the presence of invasive nonnative Tamarix. Ecological Applications 12:760-772. Stromberg J. C. 2001. Restoration of riparian vegetation in the south-western United States: importance of flow regimes and fluvial dynamism. Journal of Arid Environments 49:17-34. Thomson W. W., W. L. Berry, and L. L. Liu. 1969. Localization and secretion of salt by the salt glands of Tamarix aphylla. Proceedings of the National Academy of Science USA 63:310-317. Vandersande M. W., E. P. Glenn, and J. L. Walworth. 2001. Tolerance of five riparian plants from the lower Colorado River to salinity drought and inundation. Journal of Arid Environments 49:147-159. Vitousek, P.M. 1990. Biological invasions and ecosystem processes; towards an integration of population biology and ecosystem studies. Oikos 57:7-13. | ||||||||||||
| Posted on June 7, 2008. |