Temperature variation at fine scales of minutes to hours and ~ 1–100 m is ubiquitous in marine ecosystems and often exceeds variability at larger scales. However, we know little of how well temperatures at one location or depth can serve as proxies to represent other locations, which is important in predicting thermal patterns relevant to organismal thermal stress. We used small data loggers to record fine‐scale temporal varia...

Standardized methods for effectively and rapidly monitoring changes in the biodiversity of marine ecosystems are critical to assess status and trends in ways that are comparable between locations and over time. In intertidal and subtidal habitats, estimates of fractional cover and abundance of organisms are typically obtained with traditional quadrat-based methods, and collection of photoquadrat imagery is a standard practice....

Acquiring marine biodiversity data is difficult, costly, and time-consuming, making it challenging to understand the distribution and abundance of life in the ocean. Historically, approaches to biodiversity sampling over large geographic scales have advocated for equivalent effort across multiple sites to minimize comparative bias. When effort cannot be equalized, techniques such as rarefaction have been applied to minimize bi...

A quantitative understanding of physiological thermal responses is vital for forecasting species distributional shifts in response to climate change. Many studies have focused on metabolic rate as a global metric for analyzing the sublethal effects of changing environments on physiology. Thermal performance curves (TPCs) have been suggested as a viable analytical framework, but standard TPCs may not fully capture physiological...

The ability of an organism to alter its physiology in response to environmental conditions offers a short-term defense mechanism in the face of weather extremes resulting from climate change. These often manifest as multiple, interacting drivers, especially pH and temperature. In particular, decreased pH can impose constraints on the biological mechanisms which define thermal limits by throwing off energetic equilibrium and di...

Aim Rapid anthropogenic warming coupled with changes in land use is altering the distributions of species, with consequences for ecosystem functioning and services. It is crucial to evaluate species range shifts based on understanding of the interaction of temperature with non‐climatic factors such as habitat availability and dispersal potential. Here, we aim to investigate roles of environmental temperature, habitat availabil...

Ecologically dominant species often define ecosystem states, but as human disturbances intensify, their subordinate counterparts increasingly displace them. We consider the duality of disturbance by examining how environmental drivers can simultaneously act as a stressor to dominant species and as a resource to subordinates. Using a model ecosystem, we demonstrate that CO 2 ‐driven interactions between species can account for...

Thermal performance curves ( TPC s), which quantify how an ectotherm's body temperature ( T b ) affects its performance or fitness, are often used in an attempt to predict organismal responses to climate change. Here, we examine the key – but often biologically unreasonable – assumptions underlying this approach; for example, that physiology and thermal regimes are invariant over ontogeny, space and time, and also that TPC s a...

Although theory suggests geographic variation in species' performance is determined by multiple niche parameters, little consideration has been given to the spatial structure of interacting stressors that may shape local and regional vulnerability to global change. Here, we use spatially explicit mosaics of carbonate chemistry, food availability and temperature spanning 1280 km of coastline to test whether persistent, overlapp...

Aim To identify geographic locations where lethal temperatures and upper zonation limits of M ytilus californianus beds coincide and to determine the dominant climatic factor where lethal limits occur. Location Intertidal shores along 1500 km of the west coast of N orth A merica. Methods Lethal temperatures for M . californianus were determined using temperature‐controlled chambers in which both the magnitude and duration of e...

Ecology Letters (2012) 15 : 680–688 Abstract Climate warming experiments generally test the ecological effects of constant treatments while neglecting the influence of more realistic patterns of environmental fluctuations. Thus, little is known regarding how the temporal interaction between multiple episodes of thermal stress influences biotic interactions. We measured the sensitivity of predation rate in an intertidal sea sta...

Species range boundaries are determined by a variety of factors of which climate is one of the most influential. As a result, climate change is expected to have a profound effect on organisms and ecosystems. However, the impacts of weather and climate are frequently modified by multiple nonclimatic factors. Therefore, the role of these nonclimatic factors needs to be examined in order to understand and predict future change. M...

Studies of the impacts of climate and climate change on biological systems often attempt to correlate ecological responses with basin‐scale indices such as the North Atlantic Oscillation (NAO). However, such correlations, while useful for detecting long‐term trends, are unable to provide a mechanism linking the physical environment and ecological processes. Here we evaluate the effects of the NAO on recruitment variability of...

Although the direct effects of climate change on species distribution and abundance have become increasingly apparent, considerably less is known about the potential for thermal variations to influence community structure indirectly through altered species interactions. We examined how the low tide body temperature of the rocky intertidal sea star Pisaster ochraceus affected the rate at which this keystone species fed on the m...