Ecodomains are areas broad climatic uniformity, defined at the global level

An ecoregion is an area with major physiographic and minor macroclimatic or oceanographic variation. There are 43 ecoregion in British Columbia of which 39 are terrestrial. Ecodivsions are meant to be mapped at 1:500,000 for regional strategic planning

Ecodivisions are areas of broad climatic and physiographic uniformity, defined at the continental level.

The B.C. Conservation Data Centre’s spatial view of publicly available, known locations of species and ecological communities at risk. This spatial view is split into the "Publicly Available Occurrences" layer and "(Extirpated and Historical) Publicly Available Occurrences" layer. The Extirpated and Historical layer includes element occurrences that have a last observation date greater than 40 years ago and element occurrences that are extirpated due to general habitat loss or degradation of the environment in the area. Use the field ‘Rank Description’ to differentiate between Historical and Extirpated element occurrences in this layer. All element occurrences are polygons: the size of the polygon usually reflects the locational uncertainty associated with the source data, represented with varying sized circles. Some polygons may be larger to reflect the actual area covered by the element occurrence. The field "Representational Accuracy" is used to communicate how accurately the polygon reflects the actual area covered by the element. If you do not find an element occurrence in your area of interest, this means there are none currently mapped in the CDC database. The best way to verify whether an area contains a species or ecosystem at risk is to have do a detailed assessment of the property during the appropriate season.

Ecosection boundaries with percent protected, number of overlapping protected areas and other attributes added as a result of geoprocessing in the Protected Area System Overview (PASO) application. Protected area and park representation by ecosection provides a landscape context for natural resource planning processes such as; management plans, land use zoning, environmental risk assessment, landscape analysis, habitat supply, and management of high priority species. Ecosections are distinguished from each other by enduring characteristics such as minor physiographic and macroclimatic or oceanographic variations. For more information on ecosections and the Ecoregion Classification System see: http://www.env.gov.bc.ca/ecology/ecoregions/index.html. For important warnings about using this data for spatial analysis see the Data Quality section of the metadata

The data layer (.shp) presented is the result of an unsupervised classification method for classifying seafloor habitat in the Bay of Fundy (Northwest Atlantic, Canada). This method involves separating environmental variables derived from multibeam bathymetry (slope, bathymetric position index), backscatter, and oceanographic information (wave-shear current velocity) into spatial units (i.e. image objects) and classifying the acoustically and oceanographically separated units into 7 habitat classes (Bedrock and Boulders, Mixed Sediments, Gravelly Sand, Sand, Silty Gravel with Anemones, Silt, and Tidal Scoured Mixed Sediments) using in-situ data (imagery). Benthoscape classes (synonymous to landscape classifications in terrestrial ecology) describe the geomorphology and biology of the seafloor and are derived from elements of the seafloor that were acoustically and oceanographically distinguishable. Reference:Wilson, B.R., Brown, C.J., Sameoto, J.A., Lacharite, M., Redden, A. (2021). Mapping seafloor habitats in the Bay of Fundy to assess macrofaunal assemblages associated with Modiolus modiolus beds. Estuarine, Coastal and Shelf Science, 252. https://doi.org/10.1016/j.ecss.2021.107294Cite this data as: Wilson, B.R., Brown, C.J., Sameoto, J.A., Lacharite, M., Redden, A. Bay of Fundy Benthoscape. Published May 2023. Population Ecology Division, Fisheries and Oceans Canada, Dartmouth, N.S. https://open.canada.ca/data/en/dataset/dbabd17a-a2c7-4b3f-9bd8-a77a9c7f9c1c

The objective of this project was to gather data to develop a model of the food web of the lower trophic levels of the nearshore area of the Beaufort Sea. Sampling took place from 2005 to 2008 using the CCGS Nahidik. The multidisciplinary character of the Nahidik program produced measurements of biology/ecology (primary production, phytoplankton, zooplankton, benthos, fish), chemical and physical oceanography, contaminants, geology and hydro acoustics. The data were collected in July and August of each year. The Nahidik program provided data to provide a baseline for future studies as well as an information source for environmental assessment.

Sexual reproduction is critical to the resilience of seagrass beds impacted by habitat degradation or environmental changes, as robust seed banks allow new shoots to establish each year. Reproductive strategies of seagrass beds range on a continuum from strictly annual to perennial, driven by local environmental conditions. We examined the reproductive dynamics of Zostera marina beds at six sites on the Atlantic coast of Canada to characterize how life history strategies are shaped by the surrounding environment. Sites were categorized as wave protected and wave exposed, where protected sites were warm, shallow, with little water movement and muddy sediments, and exposed sites were either shallow or deep, with cooler water and sandy sediments. While mixed life history strategies were evident at all sites, protected eelgrass beds exhibited both the highest and lowest sexual reproductive effort relative to exposed beds. These beds regularly experienced thermal stress, with higher temperature range and extended warm water events relative to exposed beds. The development of reproductive shoots were similar across sites with comparable Growing Degree-days at the beginning and end of anthesis, but the First Flowering Date was earlier at the protected warmer sites relative to exposed sites. With different reproductive shoot density among sites, seed production, seed retention, and seedling recruitment also varied strongly. Only one site, located in a warm, shallow and protected lagoon, contained a mixed life history population with a high reproductive effort (33.7%), strong seed bank, and high seedling establishment. However, a primarily perennial population with the lowest reproductive effort (0.5%) was identified at the warmest site, suggesting that conditions here could not support high sexual reproduction. Robustness of seed banks was strongly linked to reproductive shoot density, although the role of seed retention, germination and seedling survival require further investigation. Our study provides insights into one key aspect of seagrass resilience, and suggests that resilience assessments should include reproductive shoot density to inform their management and conservation.Cite this data: Vercaemer B. and Wong M. Reproductive ecology of Zostera marina L. (eelgrass) across varying environmental conditions. Published: May 2022. Coastal Ecosystems Science Division, Fisheries and Oceans Canada, Dartmouth, N.S. https://open.canada.ca/data/en/dataset/56cfea6f-aeca-47ed-94ab-c519d9e63c91

This dataset shows the boundaries of the province's six fire management zones that existed prior to 2014 in which most forest fires received the same type of response. These management zones were based on: * common forest and forest fire management objectives * land use * density of values at risk * fire load * forest ecology The 2014 Wildland Fire Management Strategy moved from a zone-based approach to one where each wildland fire is assessed and receives an appropriate response according to the circumstances and condition of the fire.

DescriptionConservation of marine biodiversity requires understanding the joint influence of ongoing environmental change and fishing pressure. Addressing this challenge requires robust biodiversity monitoring and analyses that jointly account for potential drivers of change. Here, we ask how demersal fish biodiversity in Canadian Pacific waters has changed since 2003 and assess the degree to which these changes can be explained by environmental change and commercial fishing. Using a spatiotemporal multispecies model based on fisheries independent data, we find that species density (number of species per area) and community biomass have increased during this period. Environmental changes during this period were associated with temporal fluctuations in the biomass of species and the community as a whole. However, environmental changes were less associated with changes in species’ occurrence. Thus, the estimated increases in species density are not likely to be due to environmental change. Instead, our results are consistent with an ongoing recovery of the demersal fish community from a reduction in commercial fishing intensity from historical levels. These findings provide key insight into the drivers of biodiversity change that can inform ecosystem-based management.The layers provided represent three community metrics: 1) species density (i.e., species richness), 2) Hill-Shannon diversity, and 3) community biomass. All layers are provided at a 3 km resolution across the study domain for the period of 2003 to 2019. For each metric, we provide layers for three summary statistics: 1) the mean value in each grid cell over the temporal range, 2) the probability that the grid cell is a hotspot for that metric, and 3) the temporal coefficient of variation (i.e., standard deviation/mean) across all years.Methods:The analysis that produced these layers is presented in Thompson et al. (2022). The analysis uses data from the Groundfish Synoptic Bottom Trawl Research surveys in Queen Charlotte Sound (QCS), Hecate Strait (HS), West Coast Vancouver Island (WCVI), and West Coast Haida Gwaii (WCHG) from 2003 to 2019. Cartilaginous and bony fish species caught in DFO groundfish surveys that were present in at least 15% of all trawls over the depth range in which they were caught were included. This depth range was defined as that which included 95% of all trawls in which that species was present. The final dataset used in our analysis consisted of 57 species (Table S1 in Thompson et al. 2022).The spatiotemporal dynamics of the demersal fish community were modeled using the Hierarchical Modeling of Species Communities (HMSC) framework and package (Tikhonov et al. 2021) in R. This framework uses Bayesian inference to fit a multivariate hierarchical generalized mixed model. We modeled community dynamics using a hurdle model, which consists of two sub models: a presence-absence model and a biomass model that is conditional on presence. Our list of environmental covariates included bottom depth, bathymetric position index (BPI), mean summer tidal speed, substrate muddiness, substrate rockiness, whether the trawl was inside or outside of the ecosystem-based trawling footprint, and survey region (QCS & HS vs. WCVI & WCHG)), mean summer near-bottom temperature deviation, mean summer near-bottom dissolved oxygen deviation, mean summer cross-shore and along-shore current velocities near the seafloor, mean summer depth-integrated primary production, and local-scale commercial fishing effort.Layers are provided for three community metrics. All metrics should be interpreted as the value that would be expected in the catch from an average tow in the Groundfish Synoptic Bottom Trawl Research Surveys taken in a given 3 km grid cell. Species density (sometimes called species richness) should be interpreted as the number of the 57 species that would be caught in a trawl. Hill-Shannon diversity is a measure of diversity that gives greater weight to communities where biomass is spread equally across species. Community biomass is the total biomass across all 57 species that would be expected to be caught per square km in an average tow. Data Sources:Research data was provided by Pacific Science's Groundfish Data Unit for research surveys from the GFBio database between 2003 and 2019 that occurred in four regions: Queen Charlotte Sound, Hecate Strait, West Coast Haida Gwaii, and West Coast Vancouver Island. Our analysis excludes species that are rarely caught in the research trawls and so our estimates would not include the occurrence or biomass of these rare species.Commercial fishing data was accessed through a DFO R script detailed here: https://github.com/pbsassess/gfdata. Local scale commercial fishing effort was calculated from this data. The substrate layers were obtained from a substrate model (Gregr et al. 2021). The oceanographic layers (bottom temperature, dissolved oxygen, tidal and circulation speeds, primary production) were obtained from a hindcast simulation of the British Columbia continental margin (BCCM) model (Peña et al. 2019).Uncertainties:Species that are not well sampled by the trawl surveys may not be accurately estimated by our model. The model did not include spatiotemporal random effects, which likely underestimates spatiotemporal variability in the region. It is also important to underline covariate uncertainty and model uncertainty. The hotspot estimates provide one measure of model uncertainty/certainty.