Esteban Muldavin
University of New Mexico
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Featured researches published by Esteban Muldavin.
Landscape Ecology | 2006
Debra P. C. Peters; James R. Gosz; William T. Pockman; Eric E. Small; Robert R. Parmenter; Scott L. Collins; Esteban Muldavin
Human modification of landscapes overlying natural environmental heterogeneity is resulting in an increase in the numbers and types of ecological patches and their intervening boundaries. In this paper, we describe an operational framework for understanding and predicting dynamics of these biotic transitions for a range of environmental conditions across multiple spatial scales. We define biotic transitions as the boundary and the neighboring states, a more general definition than typically denoted by the terms boundary, ecotone, edge or gradient. We use concepts of patch dynamics to understand the structural properties of biotic transitions and to predict changes in boundaries through time and across space. We develop testable hypotheses, and illustrate the utility of our approach with examples from arid and semiarid ecosystems. Our framework provides new insights and predictions as to how landscapes may respond to future changes in climate and other environmental drivers.
Ecology | 2018
Jennifer A. Rudgers; Y. Anny Chung; Gregory E. Maurer; Douglas I. Moore; Esteban Muldavin; Marcy E. Litvak; Scott L. Collins
Understanding controls on net primary production (NPP) has been a long-standing goal in ecology. Climate is a well-known control on NPP, although the temporal differences among years within a site are often weaker than the spatial pattern of differences across sites. Climate sensitivity functions describe the relationship between an ecological response (e.g., NPP) and both the mean and variance of its climate driver (e.g., aridity index), providing a novel framework for understanding how climate trends in both mean and variance vary with NPP over time. Nonlinearities in these functions predict whether an increase in climate variance will have a positive effect (convex nonlinearity) or negative effect (concave nonlinearity) on NPP. The influence of climate variance may be particularly intense at ecosystem transition zones, if species reach physiological thresholds that create nonlinearities at these ecotones. Long-term data collected at the confluence of three dryland ecosystems in central New Mexico revealed that each ecosystem exhibited a unique climate sensitivity function that was consistent with long-term vegetation change occurring at their ecotones. Our analysis suggests that rising temperatures in drylands could alter the nonlinearities that determine the relative costs and benefits of variance in precipitation for primary production.
Journal of Vegetation Science | 2018
Martina M. Suazo; Scott L. Collins; Robert R. Parmenter; Esteban Muldavin
Changes in ecological communities are largely driven by disturbance events that take place across a variety of temporal and spatial scales (Pickett & White, 1985). These disturbances result in a mosaic of patch types that differ in age, thus creating a source of spatial and temporal heterogeneity. This is especially the case in grassland ecosystems where disturbed patches often support a species assemblage that is, for a period of time, different from that of predisturbed conditions (Collins & Smith, 2006). These patches vary in resource availability, species composition, vegetation structure and ecosystem processes within a region (Milchunas & Lauenroth, 1993; White & Jentsch, 2001). Anthropogenic disturbances such as livestock grazing (VanAuken, 2009), development (York 2011) and fire suppression (Allen, 1989; Received: 5 June 2018 | Revised: 25 July 2018 | Accepted: 2 October 2018 DOI: 10.1111/jvs.12690
Ecology | 2018
Jeff E. Houlahan; David J. Currie; Karl Cottenie; G. S. Cumming; C. S. Findlay; Samuel D. Fuhlendorf; Pierre Legendre; Esteban Muldavin; D. Noble; R. Russell; Richard D. Stevens; T. J. Willis; S. M. Wondzell
Effects of species diversity on population and community stability (or more precisely, the effects of species richness on temporal variability) have been studied for several decades, but there have been no large-scale tests in natural communities of predictions from theory. We used 91 data sets including plants, fish, small mammals, zooplankton, birds, and insects, to examine the relationship between species richness and temporal variability in populations and communities. Seventy-eight of 91 data sets showed a negative relationship between species richness and population variability; 46 of these relationships were statistically significant. Only five of the 13 positive richness-population variability relationships were statistically significant. Similarly, 51 of 91 data sets showed a negative relationship between species richness and community variability; of these, 26 were statistically significant. Seven of the 40 positive richness-community-variability relationships were statistically significant. We were able to test transferability (i.e., the predictive ability of models for sites that are spatially distinct from sites that were used to build the models) for 69 of 91 data sets; 35 and 31 data sets were transferable at the population and community levels, respectively. Only four were positive at the population level, and two at the community level. We conclude that there is compelling evidence of a negative relationship between species richness and temporal variability for about one-half of the ecological communities we examined. However, species richness explained relatively little of the variability in population or community abundances and resulted in small improvements in predictive ability.
Southwestern Naturalist | 2017
John A. Ludwig; Steven M. Wondzell; Esteban Muldavin; K. Rosalind Blanche; Yvonne Chauvin
Abstract— Due to the hotter droughts occurring with climate change, grasslands of southwestern deserts and southern plains in the United States are predicted to increasingly lose cover of native plant species, be invaded by nonnative species, and have accelerated soil erosion. We evaluated these predictions for desert grasslands in the Paint Gap Hills of Big Bend National Park, Texas. We used data from 10 monitoring transects established in 1981 and surveyed vegetation composition, canopy cover, and soil surface elevations in 1981, 1983, 1995, and 2014. Four longer and hotter droughts occurred between 1985 and 2014. We found that by 2014 canopy covers of two dominant native warm-season perennial grasses, Bouteloua curtipendula and Bouteloua ramosa, were reduced to near zero, and the cover of many native shrubs and subshrubs had notably declined. By 2014 two nonnative perennial grasses, Eragrostis lehmanniana and Pennisetum ciliare, had invaded, and their expansion could have long-term ecological consequences. Soil surfaces changed from accumulating sediments at a rate of +0.7 mm/year for 1983–1995 to eroding at −1.6 mm/year for 1995–2014. These soil and vegetation changes support predictions of major declines in native desert grasslands and emphasize their vulnerability to climate change.
Ecological Restoration | 2017
Esteban Muldavin; Elizabeth R. Milford; Nancy E. Umbreit; Yvonne Chauvin
In 1998, a riparian restoration demonstration project was initiated with a target of efficiently establishing a dynamic patch mosaic of vegetation communities along a regulated river using available water and sediment and remaining natural hydrological processes. A point bar along the Middle Rio Grande, Albuquerque, New Mexico, dominated by the nonnative shrub Elaeagnus angustifolia (Russian olive), was mechanically treated by removing all vegetation and lowering a portion of the bar to allow overbank flooding during typical spring releases from an upstream dam (Cochiti Dam). Side channels and small islands were engineered in the lowered bar to slow flood waters, aid sediment deposition, and add site complexity. After treatment, a high-resolution monitoring grid was installed to track vegetation changes. Following an initial flood in the spring of 1998, over 10,000 cottonwoods per ha naturally established, but densities varied based on the fluvial landforms. Zones that were sufficiently wetted or naturally formed behind large woody debris were the most successful, while the artificial fill zone and the portion of the bar not lowered had the least native riparian tree recruitment. Over 15 years, cottonwood numbers declined through intraspecific competition and beaver browsing at all sites, but they continued to dominate. Natives also dominated a species-rich herbaceous layer, particularly on the lowered sites. The incursion of a new herbaceous invader, Saccharum ravennae (ravennagrass), was an unexpected outcome revealed by the long-term monitoring record. Yet, based on several criteria, the site reflects a successful application of a natural-process approach to restoration that can lead to increased ecosystem complexity and resilience.
Rangeland Ecology & Management | 2009
William H. Romme; Craig D. Allen; John D. Bailey; William L. Baker; Brandon T. Bestelmeyer; Peter M. Brown; Karen S. Eisenhart; M. Lisa Floyd; David W. Huffman; Brian F. Jacobs; Richard F. Miller; Esteban Muldavin; Thomas W. Swetnam; Robin J. Tausch; Peter J. Weisberg
Oecologia | 2008
Esteban Muldavin; Douglas I. Moore; Scott L. Collins; Karen R. Wetherill; David C. Lightfoot
Journal of Arid Environments | 2001
Laura Foster Huenneke; Esteban Muldavin
Journal of Vegetation Science | 2012
Jan C. Ruppert; Alexander Holm; Sabine Miehe; Esteban Muldavin; H.A. Snyman; Karsten Wesche; Anja Linstädter