AIS NL Biofouling Species Fisheries and Oceans Canada's (DFO) National Marine Biofouling Monitoring Program conducts annual field surveys to monitor the introduction, establishment, spread, species richness, and relative abundance of native and some non-native species in Newfoundland and Labrador (NL) Region since 2006. Standardized monitoring protocols employed by DFO's NL, Maritimes, Gulf, and Quebec regions include biofouling collector plates deployed from May to October at georeferenced intertidal and shallow subtidal sites, including public docks, and public and private marinas and nautical clubs. Initially, (2006-2017), the collectors consisted of three 10 cm by 10 cm PVC plates deployed in a vertical array and spaced approximately 40 cm apart, with the shallowest plate suspended at least 1 m below the surface to sample subtidal and shallow intertidal species (McKenzie et al 2016a). Three replicate arrays were deployed at least 5 m apart per site. Since 2018, collector networks have been modified to improve statistical replication, including up to 10 individual collectors deployed per site at 1 m depth and at least 5 m apart (as above) from May to October. Since 2006, seven invasive biofouling organisms have been detected in Newfoundland and Labrador harbours, marinas and coastal areas.Should be cited as follows: DFO Newfoundland and Labrador Region Aquatic Invasive Species Marine Biofouling Monitoring Program. Published March 2024. Coastal and Freshwater Ecology, Northwest Atlantic Fisheries Centre, Fisheries and Oceans Canada, St. John’s, Newfoundland and Labrador.Reference:TunicatesVase tunicate (Ciona intestinalis) 2012 The Vase tunicate, is a high impact solitary invader and was first detected by DFO in 2012 on the Burin Peninsula at Ship Cove and Little Bay, Placentia Bay. Various mitigation measures (McKenzie et al. 2016b) contained this invasive tunicate to a small area for six years within Placentia Bay. First detected in Fortune Bay as an established population in 2019, increasing reports of the Vase tunicate have been made along the south coast of Newfoundland. The data provided here indicates the detections of this AIS in coastal NL.From 2018-2022, the Coastal Environmental Baseline Program provided additional support to enhance sampling efforts in Placentia Bay.

PURPOSE:The purpose of this work was to determine (1) how the population genomic structure relates to gut microbiota composition of White Hake (Urophycis tenuis), and (2) whether microbiota community variation provides complementary insights into population structure of this species in eastern Canada.DESCRIPTION:Integrating host-associated microbiota with genomic approaches offers an opportunity to better understand the multiple biological dimensions shaping population structure in marine fishes. A clear understanding of population structure and dynamics is essential for informed fisheries management and conservation decisions; however, while genomic approaches have greatly improved our ability to delineate biological populations, they provide only a partial representation of biological structure, as patterns of differentiation reflect both historical divergence and contemporary ecological conditions. Host-associated microbiota can influence population-level ecological processes by contributing functional, potentially heritable variation that shapes host phenotype and fitness.In this study, we combined genotyping-by-sequencing with 16S rRNA gene amplicon sequencing to examine how population genomic structure relates to gut microbiota composition and to evaluate whether microbiota community variation provides complementary insights into population structure in White Hake (Urophycis tenuis) in eastern Canada. Genomic analyses identified two populations with greater spatial overlap than previously reported. Variation partitioning revealed that host genetics explained a negligible proportion of microbiota variation compared to environmental factors and fish length, suggesting that ontogenetic shifts in habitat use and resource acquisition influence gut microbiota composition. Several taxa were differentially abundant among fish length categories used as a proxy for diet, including taxa with chitin-degrading potential such as Photobacterium and Lachnospirales, which were enriched in smaller fish known to consume a crustacean-dominated diet. Together, these results indicate that gut microbiota composition in White Hake primarily reflects ecological and life-history processes rather than host population structure. PARAMETERS COLLECTED:Environmental parameters were also collected at most sampling sites, including depth, water temperature, oxygen and salinity levels.PHYSICAL SAMPLE DETAILS:Fin samples were collected to characterize the fish genotypes. Intestine (rectum) samples were collected to study fish gut microbiome.SAMPLING METHODS:In 2022 and 2023, White Hake were sampled during Fisheries and Oceans Canada (DFO) annual bottom trawl ecosystem monitoring surveys.USE LIMITATION:To ensure scientific integrity and appropriate use of the data, we would encourage you to contact the data custodian.

This dataset provides marine bacteriological water quality data for bivalve shellfish harvest areas in New Brunswick, Canada. Shellfish harvest area water temperature and salinity data are also provided as adjuncts to the interpretation of fecal coliform density data. The latter is the indicator of fecal matter contamination monitored annually by Environment and Climate Change Canada (ECCC) within the framework of the Canadian Shellfish Sanitation Program (CSSP). The geospatial positions of the sampling sites are also provided. These data are collected by ECCC for the purpose of making recommendations on the classification of shellfish harvest area waters. ECCC recommendations are reviewed and adopted by Regional Interdepartmental Shellfish Committees prior to regulatory implementation by Fisheries and Oceans Canada (DFO).This dataset is 'Deprecated'. Please use updated source here.https://open.canada.ca/data/en/dataset/6417332a-7f37-49bd-8be9-ce0402deed2a

Groundwater flow is the movement of water in an aquifer or hydrogeological unit. The dataset shows groundwater flow rate and direction in the hydrogeological unit. Groundwater flow is establish from piezometric surface map. The method used to create the dataset is described in the metadata associated with the dataset. The dataset represents a description of the flow, including rate in m/d, direction, date and source. Typically, the data provided will not be in the form of a shapefile with linked properties but in the form of an image that sketches the groundwater flow. The image could also represent a cross section of the hydrogeologic units showing the regional trends of the groundwater flow.

An exploratory project on the taxonomic and genetic diversity of decapods in three ocean subregions (Northeast Pacific, Canadian Arctic, and Northwest Atlantic), which were sampled in 2022, was undertaken by the Arctic Working Group under the Canada-U.S. Fisheries and Climate Collaboration between Fisheries and Oceans Canada (DFO) and the National Marine Fisheries Service (NMFS) of the National Oceanic and Atmospheric Administration (NOAA). This collaboration framework aims to pool Canadian and U.S. data to explore the impacts of broad-scale climate change on marine biodiversity. In early summer 2022, a sampling protocol with the selection of targeted decapods was provided to DFO and NOAA collaborators. Targeted genera were collected from a total of 10 research programs across three ocean subregions and four marine regions. The Northeast Pacific samples were collected in the Bering Sea during the Northern Bering Sea Ecosystem and Surface Trawl Survey, and the Eastern and Northern Bering Sea Continental Shelf Bottom Trawl Survey of Groundfish and Invertebrate Fauna onboard the F/V Northwest Explorer, F/V Alaska Knight and F/V Vesteraalen. In the Western Canadian Arctic (mainly from Beaufort Sea and Amundsen Gulf), specimens were collected during DFO’s Canadian Beaufort Sea – Marine Ecosystem Assessment (CBS-MEA) survey onboard the F/V Frosti. In Eastern Canadian Arctic (mainly from Baffin Bay and Davis Strait), specimens were collected during DFO’s Knowledge and Ecosystem-Based Approach in Baffin Bay (KEBABB) survey onboard the CCGS Amundsen and DFO’s North Atlantic Fisheries Organization (NAFO) Subarea 0B survey onboard the R/V Tarajoq. In the Estuary and Gulf of St. Lawrence (EGSL), specimens were collected from coastal surveys (scallops, sea cucumber, snow crab, and whelk surveys) onboard the CCGS Leim and offshore during the Ecosystemic Survey onboard the CCGS Teleost. Decapods were collected from various sampling gears (benthic beam trawl, modified Atlantic Western IIA otter trawl, Bacalao trawl, shrimp trawl, Digby scallop dredge, or modified sea cucumber dredge) and identified to the lowest possible taxonomic level and photographed, when possible. All specimens were frozen at sea (n = 995). In the lab, the identifications were validated or refined with the photos and the frozen specimens. DNA was extracted for 87 specimens and a section of COI gene was amplified in order to be sequenced using Sanger method. Sequences were compared with existing data using The Basic Local Alignment Search Tool (BLAST) in the National Center for Bio-technology Information Nucleotide database (NCBI-nt, including the GenBank database) to compare scientific names, where available.The present dataset includes 391 decapod species occurrences. DNA was extracted for a subset of 87 specimens (COI gene); sequences are publicly available on BOLD data portal under project code DDAO (see supporting document "citations_references.csv" for more information).The data are presented in Darwin Core format and are separated in three files:The "Activité_décapodes_DDAO_decapods_event_en" file contains information about missions, stations and deployments, which are presented under a hierarchical activity structure.The "Occurrence_décapodes_DDAO_decapods_en" file contains the taxonomic occurrences.The "ADN_décapodes_DDAO_decapods_DNA_en" file contains the DNA derived data.For further details, please refer to the technical report available in the supporting document named "citations_references.csv". USE LIMITATION:To ensure scientific integrity and appropriate use of the data, we would encourage you to contact the data custodian.

This dataset contains a list of drainage superintendents who are appointed by the local municipality to manage drains constructed under the [Drainage Act, 1990](https://www.ontario.ca/laws/statute/90d17). Drainage superintendents are businesses or individuals that represent the local municipality to assist landowners to resolve their drainage concerns using the Ontario Drainage Act, 1990. This list is maintained by the Ministry of Agriculture, Food and Agribusiness (OMAFA) and includes municipality names, addresses telephone numbers, and superintendent contact information. This list is updated annually or as required throughout the year. More information about the work of drainage superintendents can be found at [Drainage Superintendents Association of Ontario (DSAO)](https://www.dsao.net/).

This dataset is comprised of locations and current information for all schools for Kindergarten to Grade 12 in British Columbia. Indicators are included for schools that offer French programs including: Core French, Early French Immersion, Late French Immersion and Francophone Program.

PURPOSE:Chlorophyll a is a photosynthetic pigment common to aquatic algae, and its measurement can provide an estimate of free-floating algae abundance in an aquatic system. For more than 40 years, the Fisheries and Oceans Canada - Great Lakes Laboratory for Fisheries and Aquatic Sciences (DFO-GLLFAS) office in Sault Ste. Marie Ontario has collected water samples for chlorophyll a spectrophotometric analysis, producing data in the form of mg/m3. The collection of chlorophyll a data was generally conducted to assist in characterizing the aquatic systems level of primary productivity, since that can influence fish abundance. This was a supplementary measure of the quality of fish habitat in these systems for a variety of fish-related projects of relevance to DFO’s mandate. Consistency of data collection was dependent on the duration of each project and funding available. DESCRIPTION:The initial study collected chlorophyll a data from the five lakes in the Turkey Lakes Watershed (TLW – Upper and Lower Batchawana Lakes, Wishart Lake, Little Turkey Lake and Turkey Lake) as well as Quinn Lake which is located outside of the TLW (see Smokorowski et al. 2006) in partnership with Environment and Climate Change Canada (ECCC) and Natural Resources Canada (NRCAN), as part of Canada’s Acid Rain Initiative. The TLW study was established in 1979 to evaluate the impacts of acid rain on terrestrial and aquatic ecosystems. This dataset encompasses chlorophyll a data collected from five lakes in the TLW and Quinn Lake (data also collected by the Canadian Wildlife Service and Environment and Climate Change Canada) from 1983 - 2010 with some gaps of varying duration (Webster et al., 2021). Note that an experimental habitat removal took place in some TLW lakes and Quinn Lake in 1999 and 2000. Specifically, in autumn of 1999, 50% of the coarse woody material was removed from the shorelines of Little Turkey Lake and Quinn Lake, and in autumn of 2000, 50% of the course woody material was removed from Wishart Lake shoreline (details available in Smokorowski et al., 2006). Methods Summary: Sampling was only conducted during the open water season and the frequency and extent of sampling frequency in each waterbody varied and was project- and funding-dependent. There are no chlorophyll a data for the years 1986, 1989 – 1990, 1996 – 1997, 2006-2007 and 2009.Sampling was accomplished by rinsing on site an appropriately-cleaned 1 L, brown-opaque polyethylene bottles at least three times. For hand draw samples, the bottle was immersed sub-surface (less than 0.5 meters) to collect the sample. Composite tube samples were collected using an integrated water sampling tube that collected epilimnion water from the entire water column to a depth of 5 meters. Up to five - 1 L (1000 mL) samples were collected per station and returned to the lab on ice. Each 1 L sample was filtered using glass fiber filters (Whatman GF/C, 42.5 mm) within one day of sampling, and then frozen prior to standard chlorophyll a analysis (American Public Health Association [APHA] 1985). From 1983-1998, Chlorophyll a concentrations (mg/L) was calculated based on APHA 1985; from 1998 to present the calculation was based on APHA (1998). The sample dataset information includes the georeferenced sampling locations, the raw data for chlorophyll a calculations, and the calculated chlorophyll a concentrations using both the APHA (1985) and APHA (1998) methods. This dataset was published in partnership with the Canadian Institute of Ecology and Evolution - Living Data Project, which was funded by a CREATE grant from the Natural Science and Engineering Research Council of Canada. We would like to recognize Caroline Dallstream for her effort in publishing this dataset. SAMPLING METHODS:Methods Summary: Sampling was only conducted during the open water season and the frequency and extent of sampling frequency in each waterbody varied and was project- and funding-dependent. There are no chlorophyll a data for the years 1986, 1989 – 1990, 1996 – 1997, 2006-2007 and 2009. See Sampling was accomplished by rinsing on site an appropriately-cleaned 1 L, brown-opaque polyethylene bottles at least three times. For hand draw samples, the bottle was immersed sub-surface (less than 0.5 meters) to collect the sample. Composite tube samples were collected using an integrated water sampling tube that collected epilimnion water from the entire water column to a depth of 5 meters. Up to five - 1 L (1000 mL) samples were collected per station and returned to the lab on ice. Each 1 L sample was filtered using glass fiber filters (Whatman GF/C, 42.5 mm) within one day of sampling, and then frozen prior to standard chlorophyll a analysis (American Public Health Association [APHA] 1985). From 1983-1998, Chlorophyll a concentrations (mg/L) was calculated based on APHA 1985; from 1998 to present the calculation was based on APHA (1998). The sample dataset information includes the georeferenced sampling locations, the raw data for chlorophyll a calculations, and the calculated chlorophyll a concentrations using both the APHA (1985) and APHA (1998) methods.USE LIMITATION:To ensure scientific integrity and appropriate use of the data, we would encourage you to contact the data custodian.

This dataset documents the epifauna occurrences collected from 2021 to 2024 during the Canadian Beaufort Sea Marine Ecosystem Assessment (CBS-MEA) conducted by the Department of Fisheries and Oceans (DFO). This scientific program focuses on the integration of oceanography, food web linkages, physical-biological couplings, and spatial and interannual variabilities. The program also aims to expand the baseline coverage of species diversity, abundances, and habitat associations in previously unstudied areas of the Beaufort Sea and Western Canadian Archipelago. The study took place mainly in the Canadian Beaufort Sea and the Amundsen Gulf. Sampling is done along transects at fixed stations in the study area. Catches are collected with a 3 m benthic beam trawl for 10 minutes bottom-contact time at a target speed of 2 knots and with a modified Atlantic Western IIA otter trawl for 20 minutes bottom-contact time at a target speed of 2.9 knots. A total of 32 stations were sampled for epifauna in 2021, 22 in 2022, 23 in 2023 and 22 in 2024, between 22-655 m depth. Epibenthic invertebrates were identified to the lowest taxonomic level possible and photographed. All unknown specimens are frozen. In the lab, the identifications are validated or refined with the photos and the frozen specimens.The data are presented in Darwin Core and are separated in two files:The "Activité_épifaune_CBSMEA_epifauna_event_en" file which contains information about missions, stations and deployments, which are presented under a hierarchical activity structure.The "Occurrence_épifaune_CBSMEA_epifauna_en" file that contains the taxonomic occurrences.

This dataset provides marine bacteriological water quality data for bivalve shellfish harvest areas in Nova Scotia, Canada. Shellfish harvest area water temperature and salinity data are also provided as adjuncts to the interpretation of fecal coliform density data. The latter is the indicator of fecal matter contamination monitored annually by Environment and Climate Change Canada (ECCC) within the framework of the Canadian Shellfish Sanitation Program (CSSP). The geospatial positions of the sampling sites are also provided. These data are collected by ECCC for the purpose of making recommendations on the classification of shellfish harvest area waters. ECCC recommendations are reviewed and adopted by Regional Interdepartmental Shellfish Committees prior to regulatory implementation by Fisheries and Oceans Canada (DFO).This dataset is 'Deprecated'. Please use updated source here.https://open.canada.ca/data/en/dataset/6417332a-7f37-49bd-8be9-ce0402deed2a