This geodatabase includes hotspot maps of 1) nearshore habitat richness, 2) diversity (fish and invertebrates), and 3) biomass (using catch per unit effort of fish and invertebrates), as well as two layers showing the spatial extent of the diversity and biomass hotspot analyses. Full details and methods can be found in the Rubidge et al. 2018 CSAS Research Document 2018/053 available here or at https://waves-vagues.dfo-mpo.gc.ca/Library/40759842.pdf. These data were reviewed as part of a Canadian Science Advisory Secretariat (CSAS) regional peer review process on Nov 1-2, 2017.Habitat Richness Hotspots: Because there are no systematic surveys of nearshore species that span the entire coastline of Northern Shelf Bioregion, the nearshore habitat richness hotspots were developed as a proxy for species diversity in nearshore areas. Habitat richness was calculated from eight habitat features: eelgrass, surfgrass, canopy-forming kelp, estuaries, areas of high rugosity, and hard, mixed, and soft substrate. The number of features within 1 km x 1 km planning units was counted, and hotspots were identified using the Getis-Ord G* tool in ArcGIS. Planning units with Gi_Bin values of 3 (99% confidence) were classified as habitat richness hotspots.Diversity and Biomass Hotspots: Hotspots of fish and invertebrate diversity and biomass were developed as proxies for spatial patterns of productivity in the Northern Shelf Bioregion. Diversity (Shannon diversity) and biomass (kg/hour or count/hook/hour) were calculated from DFO synoptic trawl and outside hard-bottom longline (HBLL) survey catch records. The outside HBLL survey was previously referred to as Pacific Halibut Management Area (PHMA) survey. The synoptic trawl and HBLL surveys have complementary spatial coverage, with the HBLL surveys occurring in more coastal areas (20–260 m) and the synoptic trawl surveys occurring on deeper shelf areas (50–1300 m). Hotspots were identified using the Getis-Ord G* tool in ArcGIS for five separate analyses: fish biomass (trawl), fish diversity (trawl), fish diversity (longline), invertebrate biomass (trawl), and invertebrate diversity (trawl). Using the Minimum Bounding Geometry Tool, convex hull polygons were drawn around groups of hotspot points (Gi_Bin values of 1, 2, or 3; confidence ≥90%) containing 10 or more points. The resulting polygons were then buffered by 1 km and manually edited where needed to exclude any large areas of the polygons that did not include hotspot points.

Monitoring data from DFO invasive species monitoring programs, along with occurrence information from online databases and the scientific literature, have been paired with high resolution environmental data and oceanographic models in species distribution models that predict present-day and project future distributions of 24 non-indigenous species (NIS) on North America`s east coast, and 31 NIS on its west coast. Future distributions were predicted for 2100, under Representative Concentration Pathway 8.5 from the Intergovernmental Panel on Climate Change’s fifth Assessment Report. Present-day and future richness of these species (i.e., hotspots) have been estimated by summing the occurrence probabilities of NIS. This data set includes the present-day and year 2100 species distribution modeling results for each species, and the estimated species richness.Cite this data as: Lyons DA., Lowen JB, Therriault TW., Brickman D., Guo L., Moore AM., Peña MA., Wang Z., DiBacco C. Data of: Updated species distribution models for marine invasive species hotspot identification. Published: November 2023. Coastal Ecosystems Science Division, Fisheries and Oceans Canada, Dartmouth, N.S. https://open.canada.ca/data/en/dataset/1439dcb3-82a6-40fd-a9a4-8f045b20ff5b

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.

Since 2005, Fisheries and Oceans Canada has been collecting monitoring data for aquatic invasive species (e.g. https://open.canada.ca/data/en/dataset/8d87f574-0661-40a0-822f-e9eabc35780d, https://open.canada.ca/data/en/dataset/503a957e-7d6b-11e9-aef3-f48c505b2a29, https://open.canada.ca/data/en/dataset/8661edcf-f525-4758-a051-cb3fc8c74423). This monitoring data, as well additional occurrence information from online databases and the scientific literature, have been paired with high resolution environmental data and oceanographic models in species distribution models that predict the present-day and future potential distributions of 12 moderate to high risk invasive species on Canada’s east and west coasts. Future distributions were predicted for 2075, under Representative Concentration Pathway 8.5 from the Intergovernmental Panel on Climate Change’s fifth Assessment Report. Present-day and future richness of these species (i.e., hotspots) has also been estimated by summing their occurrence probabilities. This data set includes the occurrence locations of each species, the present-day and future species distribution modeling results for each species, and the estimated species richness. This research has been published in the scientific literature(Lyons et al. 2020).Lyons DA, Lowen JB, Therriault TW, Brickman D, Guo L, Moore AM, Peña MA, Wang Z, DiBacco C. (In Press) Identifying Marine Invasion Hotspots Using Stacked Species Distribution Models. Biological InvasionsCite this data as: Lyons DA., Lowen JB, Therriault TW., Brickman D., Guo L., Moore AM., Peña MA., Wang Z., DiBacco C. Data of: Species distribution models and occurrence data for marine invasive species hotspot identification. Published: November 2020. Coastal Ecosystems Science Division, Fisheries and Oceans Canada, Dartmouth, N.S. https://open.canada.ca/data/en/dataset/1bbd5131-8b34-4245-b999-3b4c4259d74f

This dataset displays the Canadian geographic ranges of the priority species identified under the Pan-Canadian Approach for Transforming Species at Risk Conservation in Canada (“Pan-Canadian Approach”). These species include Barren-ground Caribou (including the Dolphin and Union population); Greater Sage-Grouse; Peary Caribou; Wood Bison; Caribou, Boreal population (“Boreal Caribou”); and Woodland Caribou, Southern Mountain population (“Southern Mountain Caribou”). The priority species were chosen following a number of criteria and considerations in collaboration with federal, provincial, and territorial partners. These include, but were not limited to, the species' ecological role on a regional or national scale, their conservation status and achievability of conservation outcomes, their social and cultural value (particularly to Indigenous peoples), and the leadership/partnership opportunities that they present. Delivering conservation outcomes for targeted priority species can have significant co-benefits for other species at risk, and wildlife in general. For more information on the Pan-Canadian Approach and the priority species, see https://www.canada.ca/en/services/environment/wildlife-plants-species/species-risk/pan-canadian-approach.html.This dataset includes: 1) the range for the Boreal Caribou (see https://species-registry.canada.ca/index-en.html#/consultations/2253); 2) the local populations for the Southern Mountain Caribou (see https://species-registry.canada.ca/index-en.html#/consultations/1309); 3) the range for the Greater Sage-Grouse (see https://species-registry.canada.ca/index-en.html#/consultations/1458); 4) local populations for the Peary Caribou (see https://species-registry.canada.ca/index-en.html#/consultations/3657); 5) range for the Barren-ground Caribou (see https://www.maps.geomatics.gov.nt.ca/Html5Viewer/index.html?viewer=NWT_SHV English only); 6) range for the Barren-ground Caribou, Dolphin and Union population (https://www.maps.geomatics.gov.nt.ca/Html5Viewer/index.html?viewer=NWT_SHV English only); 7) range for the Wood Bison (see https://species-registry.canada.ca/index-en.html#/consultations/2914).

Marine Protected Areas require comprehensive monitoring to ensure objectives are achieved; however, monitoring natural ecosystems at scale is challenged by the biodiversity it aims to measure. Environmental DNA (eDNA) metabarcoding holds promise to address this monitoring challenge. We conducted paired sampling at 54 sites for fish and invertebrate assemblages in the Northwest Atlantic using groundfish trawls and eDNA metabarcoding of benthic seawater using four genetic markers (12S rRNA, 16S rRNA, 18S rRNA, and CO1). Compared to trawling, eDNA detected similar patterns of species turnover, larger estimates of gamma diversity, and smaller estimates of alpha diversity. A total of 63.6% (42/66) of fish species captured by trawling were detected by eDNA, along with an additional 26 species. Of the 24 missed detections by eDNA, 12 were inevitable as they lacked reference sequences. Excluding taxa assigned to higher than species level and those without a species name, 23.6% (17/72) of invertebrate species captured by trawling were detected by CO1, which detected an additional 98 species. We demonstrate that eDNA is capable of detecting patterns of community assemblage and species turnover in an offshore environment, emphasizing its strong potential for a non-invasive, comprehensive, and scalable tool for biodiversity monitoring supporting marine conservation programmes.Cite this data as: Jeffery, N., Rubidge, E., Abbott, C., Westfall, K., Stanley, R. (2024): Data of: eDNA metabarcoding enriches traditional trawl survey data for monitoring biodiversity in the marine environment.Published: August 2024. Coastal Ecosystems Science Division, Fisheries and Oceans Canada, Dartmouth, N.S. https://open.canada.ca/data/en/dataset/43a91ba7-8025-4330-88db-db14022d729d

2014 to 2023 demersal fish group richness in the Estuary and Gulf of St.Lawrence estimated by the number of species found in each grid cell 10 km x 10 km. Input data are from the annual August and September multidisciplinary surveys.PurposeSince 1990, the Department of Fisheries and Oceans has been conducting an annual multidisciplinary survey in the Estuary and northern Gulf of St. Lawrence using a standardized protocol. In the southern Gulf of St. Lawrence, these bottom trawl surveys has been carrying out each September since 1971. These missions are an important source of information about the status of the marine ressources.The objectives of the surveys are multiple: to estimate the abundance and biomass of groundfish and invertebrates, to identify the spatial distribution and biological characteristics of these species, to monitor the biodiversity of the Estuary and Gulf and finally, to describe the environmental conditions observed in the area at the moment of the sampling.The southern Gulf surveys are realized using the following standardized protocol:Hurlbut,T. and D.Clay (eds) 1990. Protocols for Research Vessel Cruises within the Gulf Region (Demersal Fish) (1970-1987). Can. MS Rep. Fish. Aquat. Sci. No. 2082: 143p.The sampling protocols used for the Estuary and northern Gulf surveys are described in details in the following publications:Bourdages, H., Archambault, D., Bernier, B., Fréchet, A., Gauthier, J., Grégoire, F., Lambert, J., et Savard, L. 2010. Résultats préliminaires du relevé multidisciplinaire de poissons de fond et de crevette d’août 2009 dans le nord du golfe du Saint-Laurent. Rapp. stat. can. sci. halieut. aquat. 1226 : xii+ 72 p. Bourdages, H., Archambault, D., Morin, B., Fréchet, A., Savard, L., Grégoire, F., et Bérubé, M. 2003. Résultats préliminaires du relevé multidisciplinaire de poissons de fond et de crevette d’août 2003 dans le nord du golfe du Saint-Laurent. Secr. can. consult. sci. du MPO. Doc. rech. 2003/078. vi + 68 p.Annual reports are available at the Canadian Science Advisory Secretariat (CSAS), (http://www.dfo-mpo.gc.ca/csas-sccs/index-eng.htm).Bourdages, H., Brassard, C., Desgagnés, M., Galbraith, P., Gauthier, J., Légaré, B., Nozères, C. and Parent, E. 2017. Preliminary results from the groundfish and shrimp multidisciplinary survey in August 2016 in the Estuary and northern Gulf of St. Lawrence. DFO Can. Sci. Advis. Sec. Res. Doc. 2017/002. v + 87 p.

Species distribution models (SDMs) are tools that combine species observations of occurrence, abundance, or biomass with environmental variables to predict the distribution of a species in unsampled locations. To produce accurate predictions of occurrence, abundance or biomass distribution, a wide range of physical and/or biological variables is desirable. Such data is often collected over limited or irregular spatial scales, and require the application of geospatial techniques to produce continuous environmental surfaces that can be used for modelling at all spatial scales. Here we provide a review of 102 environmental data layers that were compiled for the entire spatial extent of Fisheries and Oceans Canada’s (DFO) Maritimes Region. Variables were obtained from a broad range of physical and biological data sources and spatially interpolated using geostatistical methods. For each variable we document the underlying data distribution, provide relevant diagnostics of the interpolation models and an assessment of model performance, and present the final standard error and interpolation surfaces. These layers have been archived in a common (raster) format at the Bedford Institute of Oceanography to facilitate future use. Based on the diagnostic summaries in this report, a subset of these variables has subsequently been used in species distribution models to predict the distribution of deep-water corals, sponges, and other significant benthic taxa in the Maritimes Region.Cite this data as: Beazley, Lindsay; Guijarro, Javier, Lirette; Camille; Wang, Zeliang; Kenchington, Ellen (2020). Characteristics of Environmental Data Layers for Use in Species Distribution Modelling in the Maritimes Region. Published July 2023. Ocean Ecosystems Science Division, Fisheries and Oceans Canada, Dartmouth, N.S. https://open.canada.ca/data/en/dataset/34a917cb-a0e3-403c-91c7-af3dc20628b1

A derivative of DFO’s benthic species survey for the Strategic Program for Ecosystem-based Research and Advice (SPERA) (open data record ID: e736c0f0-b19e-4842-903d-28bfc756d48a), this benthic survey funded through the Canadian Healthy Oceans Network (CHONeII) looks at the presence/absence and abundance of two biogenic habitat-forming species that are listed as vulnerable to disturbance in a subset of 50 drift camera transects in the ‘Head Harbour/West Isles Archipelago/The Passages’ Ecologically and Biologically Significant Area (EBSA) in the Bay of Fundy, New Brunswick, Canada (~113km2). Presence/absence and abundance data of the stalked sea squirt (Boltenia ovifera) and horse mussel (Modiolus modiolus) were derived from the use of high-resolution Nikon D800 36.1 megapixel still images (n=2576, see link to parent record for more descriptive survey information) to be used in species distribution modelling. Image field of view (FOV) was estimated using a 10 cm-wide trigger weight for scale,and standardized across images using the average FOV estimate (0.75 x 0.5 m) across a subset of 200 images. Species counts were then converted to abundance estimates (number of individuals per square-meter) by dividing counts by 0.375m2. Boltenia ovifera was observed at densities reaching 456 ind./m2, while Modiolus modiolus density reached a maximum of 240 ind./m2.Cite this data as: Mireault C.A., Lawton P., Devillers R. and Teed L. Presence/absence and abundance of vulnerable marine ecosystem species Boltenia ovifera and Modiolus modiolus in the lower Bay of Fundy derived from high resolution still imagery. Published September 2023. Coastal Ecosystems Science Division, Fisheries and Oceans Canada, St. Andrews, N.B. https://open.canada.ca/data/en/dataset/152ae3f1-d2b9-43d9-a7b4-d769d9e9fc41

Polar cod (Boreogadus saida), Atlantic cod (Gadus morhua), and Greenland cod (Gadus macrocephalus) are prominent gadid species within the northwest Atlantic Ocean in terms of their ecological and socio-economic importance but it is unclear how climate-induced changes in ocean temperature may alter their distributions by the end of the century (2100). We used physiologically based species distribution models to predict how ocean warming will influence the availability of suitable habitat for early life-stages in these marine gadids. We applied CMIP5 ocean temperature projections to egg survival and juvenile growth models for Polar cod, Atlantic cod, and Greenland cod to create predicted suitability raster surfaces for these metrics across four climatology periods (1981–2005, 2026–2050, 2051–2075, 2076–2100). The analysis focused on the projected changes in temperature in ocean shelf areas where ocean depth is ≤400 m. We created an integrated habitat suitability index by combining the suitability surfaces for egg survival and growth potential to predict areas and periods where thermal conditions were suitable for both life stages. The resulting surfaces indicate that suitable thermal habitat for the juvenile life stages of all three species will shift poleward, but the magnitude of the shift and the overall area of thermally suitable habitat remaining will differ across species and life stages through time. Modelled layers are provided in NetCDF format by metric (egg survival, growth potential, habitat suitability). Data layers for Polar cod, Atlantic cod, and Greenland cod are included within each NetCDF file as variables across time. Note that in this study we refer to Gadus macrocephalus/ogac as Greenland cod since Gadus ogac is thought to be a junior synonym of Gadus macrocephalus (Carr et al., 1999). For more details on the methods and results for this analysis see Cote et al. (2021).References:Carr, S. M., Kivlichan, D. S., Pepin, P., & Crutcher, D. C. (1999). Molecular systematics of gadid fishes: implications for the biogeographic origins of Pacific species. Canadian Journal of Zoology, 77(1), 19–26. https://doi.org/10.1139/cjz-77-1-19Cote, D., Konecny, C. A., Seiden, J., Hauser, T., Kristiansen, T., & Laurel, B. J. (2021). Forecasted Shifts in Thermal Habitat for Cod Species in the Northwest Atlantic and Eastern Canadian Arctic. Frontiers in Marine Science, 8(November), 1–15. https://doi.org/10.3389/fmars.2021.764072