Recent global policy initiatives aimed at reducing forest degradation require practical definitions of degradation that are readily monitored. However, consistent approaches for monitoring forest degradation over the long term and at broad scales are lacking. We quantified the long‐term effects of intensive wood harvest on above‐ground carbon and biodiversity at fine resolutions (30 m 2 ) and broad scales (New Brunswick, Canad...

Bacterioplankton underpin biogeochemical cycles and an improved understanding of the patterns and drivers of variability in their distribution is needed to determine their wider functioning and importance. Sharp environmental gradients and dispersal barriers associated with ocean fronts are emerging as key determinants of bacterioplankton biodiversity patterns. We examined how the development of the Celtic Sea Front (CF), a ti...

Can we predict long‐term trends of lake surface temperature based on air temperature alone? We explore this question by analyzing the performance of a hybrid model ( air2water ) as a predictive tool for defining scenarios of lake surface temperature in the framework of climate change studies. Employing Lake Tahoe (U.S.A.) as a case study, we apply the model using different air temperature datasets (in situ measurements, gridde...

Forest degradation in the tropics is often associated with roads built for selective logging. The protection of intact forest landscapes (IFL) that are not accessible by roads is high on the biodiversity conservation agenda and a challenge for logging concessions certified by the Forest Stewardship Council (FSC). A frequently advocated conservation objective is to maximize the retention of roadless space, a concept that is bas...

Aim Tropical forests store 25% of global carbon and harbour 96% of the world's tree species, but it is not clear whether this high biodiversity matters for carbon storage. Few studies have teased apart the relative importance of forest attributes and environmental drivers for ecosystem functioning, and no such study exists for the tropics. Location Neotropics. Methods We relate aboveground biomass ( AGB ) to forest attributes...

Approximately 200 km from the mouth of the Fraser River, British Columbia, Canada, adult sockeye salmon Oncorhynchus nerka , were gastrically implanted with radio transmitters without anaesthetic. Subsets of the transmitter implanted fish were also biopsied which included drawing blood from the caudal peduncle (3 ml), removal of gill tissue (0·03 g) and quantification of energetic status using a microwave fat meter. Several ex...

Depending on population, wild Fraser River sockeye salmon Oncorhynchus nerka travel distances of 1100 km and ascend elevations ranging from near sea‐level to 1200 m to reach spawning areas. Populations embarking on distant, high elevation migrations ( i.e . Early Stuart, Chilko and Horsefly populations) began their upriver spawning migrations with higher densities of somatic energy ( c . 9·2 to 9·8 MJ kg −1 ) and fewer eggs (...

Releasing a population of adult Fraser River sockeye salmon Oncorhynchus nerka from an energetically more expensive non‐feeding natural migration (1089 km, natal groups) and allowing them to sexually mature in either a moderate flow (captive exercise group) or a no flow (captive non‐exercise group) environment resulted in significant differences in body energy densities (MJ kg −1 ) among groups (ranked: initial natural migrato...

Novel field measurements of critical swimming speed ( U crit ) and oxygen uptake ( M o 2 ) in three species of adult Pacific salmon Oncorhynchus spp. up to 3·5 kg in body mass were made using two newly designed, mobile Brett‐type swim tunnel respirometers sited at a number of field locations in British Columbia, Canada. Measurements of U crit , which ranged from 1· 68 to 2·17 body lengths s −1 , and maximum M o 2 , which range...