Mauricio Lima

Mauricio Lima

orcid

Research Focus & Metrics

Academic Career Length

32Years (1995-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

View All Publications
23 August 2002 in Science
Verified
Journal Article
Closed access
PDF file
NSNils Chr. Stenseth
Nils Chr. Stenseth
AMAtle Mysterud
Atle Mysterud
GOGeir Ottersen
Geir Ottersen
JHJames W. Hurrell
James W. Hurrell
KCKung-Sik Chan
Kung-Sik Chan
MLMauricio Lima
Mauricio Lima
Climate influences a variety of ecological processes. These effects operate through local weather parameters such as temperature, wind, rain, snow, and ocean currents, as well as interactions among these. In the temperate zone, local variations in weather are often coupled over large geographic areas through the transient behavior of atmospheric planetary-scale waves. These variations drive temporally and spatially averaged exchanges of heat, momentum, and water vapor that ultimately determine growth, recruitment, and migration patterns. Recently, there have been several studies of the impact of large-scale climatic forcing on ecological systems. We review how two of the best-known climate phenomena—the North Atlantic Oscillation and the El Niño–Southern Oscillation—affect ecological patterns and processes in both marine and terrestrial systems.

22 October 2003 in Proceedings Of The Royal Society B-Biological Sciences
Verified
Journal Article
Closed access
PDF file
NSNils Chr. Stenseth
Nils Chr. Stenseth
GOGeir Ottersen
Geir Ottersen
JHJames W. Hurrell
James W. Hurrell
AMAtle Mysterud
Atle Mysterud
MLMauricio Lima
Mauricio Lima
BÅBjørn Ådlandsvik
Bjørn Ådlandsvik
Whereas the El Niño Southern Oscillation (ENSO) affects weather and climate variability worldwide, the North Atlantic Oscillation (NAO) represents the dominant climate pattern in the North Atlantic region. Both climate systems have been demonstrated to considerably influence ecological processes. Several other large–scale climate patterns also exist. Although less well known outside the field of climatology, these patterns are also likely to be of ecological interest. We provide an overview of these climate patterns within the context of the ecological effects of climate variability. The application of climate indices by definition reduces complex space and time variability into simple measures, ‘packages of weather’. The disadvantages of using global climate indices are all related to the fact that another level of problems are added to the ecology–climate interface, namely the link between global climate indices and local climate. We identify issues related to: (i) spatial variation; (ii) seasonality; (iii) non–stationarity; (iv) nonlinearity; and (v) lack of correlation in the relationship between global and local climate. The main advantages of using global climate indices are: (i) biological effects may be related more strongly to global indices than to any single local climate variable; (ii) it helps to avoid problems of model selection; (iii) it opens the possibility for ecologists to make predictions; and (iv) they are typically readily available on Internet.

30 December 2005 in Proceedings of the National Academy of Sciences
Verified
Journal Article
Closed access
MAMatías Arim
Matías Arim
SASebastián R. Abades
Sebastián R. Abades
PNPaula E. Neill
Paula E. Neill
MLMauricio Lima
Mauricio Lima
PMPablo Marquet
Pablo Marquet
Species invasions are a principal component of global change, causing large losses in biodiversity as well as economic damage. Invasion theory attempts to understand and predict invasion success and patterns of spread. However, there is no consensus regarding which species or community attributes enhance invader success or explain spread dynamics. Experimental and theoretical studies suggest that regulation of spread dynamics is possible; however, the conditions for its existence have not yet been empirically demonstrated. If invasion spread is a regulated process, the structure that accounts for this regulation will be a main determinant of invasion dynamics. Here we explore the existence of regulation underlying changes in the rate of new site colonization. We employ concepts and analytical tools from the study of abundance dynamics and show that spread dynamics are, in fact, regulated processes and that the regulation structure is notably consistent among invasions occurring in widely different contexts. We base our conclusions on the analysis of the spread dynamics of 30 species invasions, including birds, amphibians, fish, invertebrates, plants, and a virus, all of which exhibited similar regulation structures. In contrast to current beliefs that species invasions are idiosyncratic phenomena, here we provide evidence that general patterns do indeed exist.

5 September 2013 in Oikos
Verified
Journal Article
Closed access
PDF file
SESergio A. Estay
Sergio A. Estay
MLMauricio Lima
Mauricio Lima
FBFrancisco Bozinovic
Francisco Bozinovic


1 July 2009 in Ecology
Verified
Journal Article
Open access
PDF file
APAndrea Previtali
Andrea Previtali
MLMauricio Lima
Mauricio Lima
PMPeter L. Meserve
Peter L. Meserve
DKDouglas A. Kelt
Douglas A. Kelt
JGJulio R. Gutiérrez
Julio R. Gutiérrez
Precipitation plays an important role in the dynamics of species found in arid and semiarid environments. However, population fluctuations generally are driven by a combination of multiple factors whose relative contribution may vary through time and among species. We monitored fluctuations of species in three trophic levels for >17 years at a semiarid community in north‐central Chile. The region is strongly affected by the El Niño Southern Oscillation, resulting in high variation in rainfall that triggers dramatic changes in food resource availability, with strong effects on upper trophic levels. We focused our analyses on the role played by endogenous and exogenous (climatic) factors on the dynamics of two important rodent species in the community, Octodon degus and Phyllotis darwini. We documented population fluctuations of several orders of magnitude in response to wet and dry episodes of different strength and duration. P. darwini reached similar maximum densities, regardless of the duration of high‐rainfall events, whereas O. degus showed additive effects of multiple wet years. Time series diagnostic tools revealed oscillations with a 5‐year periodicity in rainfall, which may be the cause of the same periodicity and a weak second‐order signal observed in the rodent dynamics. However, the dynamics of both rodent species were dominated by strong first‐order processes, suggesting an important role of direct density dependence. Intraspecific competition, expressed as the ratio of rodent density/rainfall (or food resources) explained more than two‐thirds of the variation in the population rate of change, whereas less than one‐third was explained by lagged rainfall (or food resources). We detected no significant effects of predation. Our results contribute to a growing number of examples of dynamics governed by the combined effect of density dependence and climatic forcing. They also reveal strong bottom‐up regulation that may be common in other arid environments.