Next Article in Journal
Simultaneous Determination of Fluorine and Chlorine in Marine and Stream Sediment by Ion Chromatography Combined with Alkaline Digestion in a Bomb
Next Article in Special Issue
A Review of Modeling Approaches for Understanding and Monitoring the Environmental Effects of Marine Renewable Energy
Previous Article in Journal
Ciphered BCH Codes for PAPR Reduction in the OFDM in Underwater Acoustic Channels
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Article

What’s in My Toolkit? A Review of Technologies for Assessing Changes in Habitats Caused by Marine Energy Development

by
Lenaïg G. Hemery
1,*,
Kailan F. Mackereth
1 and
Levy G. Tugade
2
1
Pacific Northwest National Laboratory, Coastal Sciences Division, Sequim, WA 98382, USA
2
Pacific Northwest National Laboratory, Coastal Sciences Division, Seattle, WA 98109, USA
*
Author to whom correspondence should be addressed.
J. Mar. Sci. Eng. 2022, 10(1), 92; https://doi.org/10.3390/jmse10010092
Submission received: 4 November 2021 / Revised: 16 December 2021 / Accepted: 4 January 2022 / Published: 11 January 2022

Abstract

:
Marine energy devices are installed in highly dynamic environments and have the potential to affect the benthic and pelagic habitats around them. Regulatory bodies often require baseline characterization and/or post-installation monitoring to determine whether changes in these habitats are being observed. However, a great diversity of technologies is available for surveying and sampling marine habitats, and selecting the most suitable instrument to identify and measure changes in habitats at marine energy sites can become a daunting task. We conducted a thorough review of journal articles, survey reports, and grey literature to extract information about the technologies used, the data collection and processing methods, and the performance and effectiveness of these instruments. We examined documents related to marine energy development, offshore wind farms, oil and gas offshore sites, and other marine industries around the world over the last 20 years. A total of 120 different technologies were identified across six main habitat categories: seafloor, sediment, infauna, epifauna, pelagic, and biofouling. The technologies were organized into 12 broad technology classes: acoustic, corer, dredge, grab, hook and line, net and trawl, plate, remote sensing, scrape samples, trap, visual, and others. Visual was the most common and the most diverse technology class, with applications across all six habitat categories. Technologies and sampling methods that are designed for working efficiently in energetic environments have greater success at marine energy sites. In addition, sampling designs and statistical analyses should be carefully thought through to identify differences in faunal assemblages and spatiotemporal changes in habitats.

1. Introduction

In numerous countries around the world, regulatory authorities require that potential impacts on the marine environment are assessed prior to industrial development at sea, which includes activities such as offshore drilling, dredging, or installing marine energy infrastructure. For example, European countries are held by the European Water Framework Directive [1], Habitat Directive [2], and Marine Strategy Framework Directive [3] to monitor the status of the ecological quality of freshwater and saltwater bodies and the various habitats they host, and to maintain the sustainable use of these water bodies. In the United States (U.S.), water quality is regulated by the Clean Water Act [4] and associated acts, while habitats and species of special concern are regulated by various policies such as the Endangered Species Act [5], Fish and Wildlife Coordination Act [6], and Magnuson–Stevens Fishery Conservation and Management Act [7]. In accordance with these regulations, environmental monitoring requirements for marine energy projects often include the identification and measurement of changes in benthic and pelagic habitats and, while long-term surveys are necessary to rule out extreme and rare events from occasional samplings, settling on the appropriate sampling technologies, methods, and analyses is as important as the spatiotemporal coverage to identify changes [8,9]. For instance, sampling gear such as grabs and statistical analyses able to describe the sediment community composition are usually recommended when documenting and monitoring environmental changes due to marine pollution [10,11]. In addition, biological communities are dynamic systems that change over time until reaching a state of persistence, a certain level of equilibrium that allows for temporal variation [12,13], which needs to be taken into account when designing and interpreting the results of surveys.
Scientists interested in marine ecology have characterized marine habitats for many decades using a great diversity of technologies and methods, in one of the oldest disciplines in marine sciences. In some places, there are local preferences and long histories of developing and using specific technologies. Over time, field sampling studies have been organized into four different types (i.e., baseline, impact, monitoring, and ecological pattern and process [14]), with some technologies being more suitable than others for specific habitats and field sampling studies. The diversity of sampling tools available for characterizing habitats and measuring changes range from gear inspired by or similar to artisanal and commercial fishing equipment, to sophisticated and constantly perfected acoustic and optical technologies [8,15,16]. Acoustic techniques for characterizing seafloor and sediment properties often require ground-truthing with physical sampling or optical imaging technologies, especially when monitoring physical disturbances due to anthropogenic activities at sea [17]. Choosing the right technology depends on the goal of the study and the habitat and depth targeted, but also on a trade-off between sample size, number of replicates, and field costs [11].
To help scientists pick the appropriate technologies and design their sampling methodologies, many institutions have established guidelines and recommendations that address various habitats, industries, and categories of technologies. Two sets of guidelines created by the International Organization for Standardization (ISO) aim to assist with quality assurance and the standardization of monitoring surveys for soft-bottom macrofauna (ISO 16665 [18]) and hard-substrate communities (ISO 19493 [19]) by recommending sampling strategies related to the habitats covered. In the U.S., while the U.S. Environmental Protection Agency (EPA) has published guidance manuals for testing dredge material [20] and on sampling designs for environmental data collection [21], the Bureau of Ocean Energy Management (BOEM, formerly the Minerals Management Service [MMS]) has released a number of guidelines and notices to lessees targeting various ocean industries and a diversity of habitats: biological survey and report requirements [22], shallow hazards [23], biologically sensitive underwater features and areas [24], deep-water benthic communities [25], benthic habitat surveys [26], fisheries related to renewable energy development [27], and geophysical, geotechnical, and geohazard guidelines [28]. In the United Kingdom, the Centre for Environment, Fisheries and Aquaculture Science (CEFAS) has established guidelines for benthic studies at dredging sites [29] and data acquisition to support marine energy projects [30], and the Joint Nature Conservation Committee (JNCC) has published a marine monitoring handbook that presents numerous procedural guidelines, including topics such as acoustic seabed mapping, side-scan sonar, sediment profile imagery, towed imagery, and sediment grabs [31].
Despite these guidelines and manuals, identifying habitat changes resulting from human activities such as marine energy development has proven to be a challenging task, particularly due to the high-energy environments targeted by this industry (i.e., channels that have strong tidal currents or open coasts that have large waves). In addition, environmental impact assessments and monitoring plans are often industry-, site-, and project-specific, which makes it difficult to compare protocols and results and transfer lessons learned from one project to another [32,33]. If not standardization, at least consistency in technologies and methods used would facilitate baseline surveys and environmental monitoring, and ultimately the development and permitting of marine energy projects [33,34]. In challenging environments such as those suitable for marine energy projects, traditional sampling and surveying technologies may prove to be inappropriate and lead to sampling bias and inaccuracies, analogous to issues highlighted when monitoring fish around artificial aggregating devices (e.g., [35]). Innovative methods and technologies may sometimes be required, however, the consistency of the data and results and the affordability of new technologies remain to be assessed [36,37].
The goal of the present literature review is to provide parties involved in surveying and monitoring the environmental effects of marine energy development, and in particular, wave and tidal energy projects, with an overview of the technologies commonly used for characterizing habitats and assessing changes associated with marine energy projects, and to understand why some technologies are selected over others. We reviewed journal articles, survey reports, and grey literature to extract information about the instruments used, their characteristics, and the methodologies as well as the performance and effectiveness of these technologies. We investigated documents describing field methods for baseline characterization and monitoring surveys at marine energy sites, but also at offshore wind farms, oil and gas offshore sites, and other marine industries around the world over the last 20 years. The aim of this review was to highlight the pros and cons of each technology as they apply (or not) to the marine energy context in the U.S., in order to help parties involved with site characterization and monitoring select the most appropriate technology(ies) for a specific marine energy project. Determining what habitats to survey and what constitutes a change can sometimes be challenging. For the purpose of this study, we considered a change to be any difference in state before and after a specific event, or any sudden or gradual transformation through space and time. Because a habitat is the natural environment of an organism comprising the array of physical and biological resources necessary to its survival and reproduction [38], we considered changes in seafloor and sediment characteristics, benthic and pelagic communities, and biofouling assemblages.

2. Materials and Methods

2.1. Literature Review

The initial search for literature describing methodologies and technologies employed for characterizing changes in habitat was carried out in the Tethys online knowledge base (https://tethys.pnnl.gov; accessed on 31 March 2021 [39]), and involved screening all past and current marine energy project sites around the world that were listed in the knowledge base as of August 2020. All research articles, environmental impact assessment documents, and baseline and monitoring survey reports publicly available in English associated with these project sites were reviewed. Useful references cited in these documents were also examined when available in English. In addition, relevant literature cited in the 2016 and 2020 State of the Science reports about the environmental effects of marine energy development around the world (respectively [40,41]) was also examined. Once the marine energy literature was evaluated, we also assessed documents related to marine industries that have analogous effects on habitats such as offshore wind, oil and gas activities, dredging, cable laying, and offshore aquaculture, with a main focus on U.S. waters. We first explored websites from U.S. environmental regulatory agencies (e.g., BOEM, National Oceanic and Atmospheric Administration, U.S. Geological Survey) for baseline and monitoring survey reports. We then completed the investigation with a keyword search in Web of Science (https://apps.webofknowledge.com; accessed on 31 March 2021) using 15 sets of keywords about marine energy, analogous industries, monitoring technologies, and habitats as well as various combinations of these sets to narrow down the results. The relevance of the articles listed by each combination returning fewer than 100 entries was gauged by reading titles and abstracts. Finally, we hand-picked a selection of research articles in the general field of marine ecology if they described relevant fieldwork methodologies, especially if applied in environments similar to those targeted by marine energy development or describing new technologies for characterizing the expected changes in habitat.
Extracted information from the reviewed documents was organized into six main habitat categories: seafloor (e.g., bathymetry, topography), sediment (e.g., sediment type, mean grain size), infauna (i.e., animal species living within the sediment), epifauna (i.e., animal species living on top of the sediment), pelagic (i.e., animal species living in the water column; here limited to fish), and biofouling (i.e., organisms growing on artificial structures). Within each of these habitat categories, 15 fields of information were filled for each document (Table 1). Some fields covered the document’s metadata, others covered technical aspects of the technologies and methods described in the documents, and others feedback about and the usability of technologies and/or data obtained.

2.2. Information Synthesis

Once all documents were reviewed, the information extracted for six of the fields (technology, reason for selecting technology, sampling design, data processing, successful identification of change, and feedback after use) was synthesized per habitat category. To do so, entries for four of these fields were assigned a group option (Table 2), based on the information provided in the documents or on our expert judgment. Sometimes, entries could be assigned to more than one group and were thus given a primary and secondary group. Entries from the technology field were sorted into broad technology classes. Most common data analyses and software were synthesized from the data processing field per habitat category.
We considered any technology or suite of sensors that were specifically assembled, adapted, or modified for the goal of the reviewed studies, or by the studies’ authors for multiple related projects, to be “custom-made”, as opposed to commercial technologies readily available off the shelf. “Historically or geographically preferred” was attributed to cases in which technologies were selected for the results to be comparable to long-term assessments, or to studies conducted many years ago or carried out in nearby areas. We cataloged as “opportunistic” any use of technology or data obtained from a third-party (e.g., industrial routine survey of structures). “Ubiquitous” was used for technologies that were somewhat wide-ranging and could be applied to various study goals, habitats, or sampling designs.
The options for categorizing sampling designs were based on the most common designs used in marine ecology [18,19,21]. Before after control impact (BACI) and control/response (CR) refer to sampling designs that look at highlighting differences between impact and reference sites on a temporal and/or spatial scale. A gradient design usually refers to increasing distance or depth from an impact site. Stratification is a design where sampling locations are distributed throughout the diversity of habitats and/or depth previously known in the study area. Several studies did not use these well-defined sampling designs; instead, they followed transects to canvas an area, collected unclassified stations (i.e., not impact or control sites) randomly or on a predefined grid, or any other design that could not easily be classified. Often, two or more sampling designs were used in conjunction (e.g., stratification with transects, before/after gradient with stations).
Several of the documents reviewed for this study focused on characterizing baseline habitats before any project (e.g., marine energy or offshore wind developments) would start, sometimes highlighting differences in habitats. Others focused on detecting whether changes and/or differences in habitats and communities were observed after an event or as distance increases from a point of impact (e.g., artificial structure, dredge material dump site). “No information” was used for studies that did not provide details about whether they looked at detecting changes or differences in habitats. Here, too, two or more group options were sometimes applicable at the same time (e.g., a baseline study that identified different communities of mobile epifauna but no difference in sessile epifauna).
Not all documents reviewed here provided feedback on their use of specific technologies, but when they did, the feedback was classified as either positive (e.g., the gear provided good quality samples in challenging settings), negative (e.g., the technology was difficult to maneuver underwater), or neutral (e.g., the instrument worked as expected). For several studies, the feedback could be classified as a combination of two or three options, when it was positive for some aspects of the work, negative for others, and neutral for yet others.
Results from the six fields of information analyzed were presented either as bar plots based on group option percentages, or as heatmaps based on the frequencies of entries. As much as possible, results are presented and discussed in the following sections by habitat category.

3. Results

A total of 259 documents were reviewed (Appendix A); of them, 139 pertained to marine energy, 24 to offshore wind, 44 to extraction activities (e.g., oil, gas, dredging), and 52 to more general topics. Numerous documents described the use of technologies related to more than one habitat category, which resulted in 533 entries. In this review, 83 entries were found to be related to the seafloor, 117 entries to sediment, 64 to infauna, 139 to epifauna, 96 to pelagic, and 34 to biofouling.
The review highlighted that as many as 120 different technologies were used across the six habitat categories, which were organized into 12 broad technology classes: acoustic, corer, dredge, grab, hook and line, net and trawl, plate, remote sensing, scrape samples, trap, visual, and others (Table 3, Figure 1). Visual was the most diverse technology class, including surveys with divers, remotely operated vehicles (ROVs), and drop or towed cameras, among others. Not all technologies were employed within each habitat category and some technologies were more commonly used than others (Figure 1 and Figure 2). Acoustic technologies, especially echosounders (e.g., fisheries echosounders, multibeam echosounders [MBESs]), were the main means of characterizing the seafloor and pelagic communities, although visual technologies were also common for pelagic habitats (e.g., divers and ROVs). Reflecting the diversity of the market, several different brands and models of MBESs and side-scan sonars were used to assess seafloor characteristics; the most common MBES brands were Kongsberg, Reson, and R2 Sonics, and EdgeTech and Klein for side-scan sonars. Acoustic technologies for characterizing pelagic communities were mainly acoustic cameras (mostly the ARIS, Imagenex, or Sound Metrics brands) and fisheries echosounders (predominantly the Simrad brand). Corers (mostly the box corer and Gray O’Hare corer) and grabs (primarily Van Veen grab, but also Day, Hamon, Shipek, and Smith–McIntyre grabs) were only used for sampling sediment and infauna. Visual technologies such as drop camera and sediment profile imaging (SPI; with or without plan view) were also often employed for these two habitat categories. Dredges (pipe or scallop dredge) were more prominently used for sampling infauna but also a few times for sampling sediment and epifauna. While several studies used nets and trawls (mainly beam trawls) to sample epifauna, and a few used traps, most of the technologies fell within the visual class, with a predominance of ROV. Many different brands and models of ROVs were used, from micro-ROVs (e.g., VideoRay) to work class types (e.g., ROPOS), and most of them featured at least high-resolution still and/or video cameras, lights, and sizing lasers. Characteristics such as depth rating, ability to collect samples, or positioning system varied greatly among ROV models. Benthic video sleds, drop cameras, and towed cameras were often of various shapes and sizes, made of a light-weight frame, and carried high-resolution still and/or video cameras facing downward (drop camera) and/or forward (sleds and towed cameras). Visual technologies were also the most common tools for assessing biofouling communities (mainly photos and videos collected in situ by divers or onshore collectors), although scrape samples, plates, and traps were also used.
Few reviewed documents explicitly stated the authors’ reasons for choosing a specific technology over other available options, but we could often assess the motives from the characteristics of the technologies, or the description of the methodologies employed (Figure 3). Over 50% of the time, the technology was ubiquitous enough to handle the specificities of the sites monitored in the reviewed studies (e.g., MBESs, ROVs). The preference for ubiquitous technologies even reached 90% of the studies that surveyed seafloor characteristics. About 30% of the studies looking at pelagic communities used historically and/or geographically preferred technologies. These were mainly various types of nets and trawls that have been used for decades (often centuries) for targeting particular species and/or environments (e.g., beach seine for sampling from shore). In roughly 25% of the studies assessing changes in epifauna and biofouling communities, and 20% of the documents describing sediment or pelagic habitats, the technologies employed were custom-made. Often, these were drop or towed cameras and the frame and suite of sensors were specifically assembled by the teams conducting the surveys, or pots and traps were modified to target and keep all sizes of specific species. Lastly, opportunistic uses of a technology were less common, except for monitoring biofouling communities, and frequently corresponded to underwater video footage acquired during routine maintenance activities around oil and gas installations, pipelines, or cables, and provided to researchers for their studies (e.g., [42,43,44]). Observers on commercial or recreational fishing boats were also classified as opportunistic.
The sampling designs employed by the reviewed studies varied greatly among technologies and habitats (Figure 4). Often, there was a primary sampling design and a secondary (e.g., BACI or CR as a primary, using transects). The transect was the predominant sampling design for surveying the seafloor, epifauna, and pelagic habitats, followed by other (often a random design), and BACI/CR for epifauna and pelagic, which are sampling designs more suitable for use with echosounders, ROVs, or towed cameras. Unclassified stations were the main sampling design for both sediment and infauna characterization, followed by transect and some sort of stratified design (stratified stations and BACI/CR stratified) for sediment, and other (often a random design) for infauna. These sampling designs are more suitable for use with corers, grab samplers, SPIs, or drop cameras. When specified, the sampling design for surveying biofouling communities was often random or opportunistic visual inspections or scrape samples, along with some stratified, gradient, or BACI/CR designs.
A good proportion of the studies concentrated on the baseline characterization of five habitat categories (all but biofouling) without focusing on detecting changes or differences: over 50% when looking at seafloor characteristics; about 30% for sediment, infauna, and epifauna; and about 15% for pelagic (Figure 5). These baseline studies may have identified diverse habitats throughout their focus area but did not report on the differences observed. In addition, a limited number of baseline studies indicated the observation of differences within the sediment, infauna and epifauna habitats that they surveyed. However, the majority of the remaining (non-baseline) studies for sediment, infauna, and epifauna, and about half for pelagic, were able to detect changes or differences in habitats and communities. Most of the studies investigating biofouling communities identified changes among the samples and/or over time. The technologies that were the most able to detect changes in habitat were side-scan sonars for seafloor characteristics (used in 16 out 83 entries), SPI and Van Veen grabs for sediment (used in 15 and 14 out of 117 entries, respectively), Van Veen grabs for infauna (used in 11 out of 64 entries), ROVs and divers (equipped or not with imagery tools) for epifauna (used in 24 and 14 out of 139 entries, respectively), fisheries echosounders and divers for pelagic communities (used in 14 and 10 out of 96 entries, respectively), and scrape samples for biofouling (used in five out of 34 entries).
While about half of the studies did not provide feedback on the sampling technologies they used, those that did varied between fully positive, fully negative, neutral, and a mix of each (Figure 6). The greatest proportion of positive feedback was for technologies used to survey seafloor characteristics such as MBESs and side-scan sonars, as well as infauna communities (no dominant technology). Examples of feedback include: “Multi-frequency side-scan sonar and the introduction of color to the processed imagery has improved classification of the seabed as compared with single frequency data” [45]; and “The Hamon grab provided point-sample information on fauna and sediment composition. These data allowed a quantitative analysis over the different areas and, to a degree, identified changes occurring within and in the near vicinity of the disposal site between 2002–2004” [17]. On the other hand, the greatest proportion of negative feedback was for technologies used to survey sediment characteristics such as SPI and Van Veen grabs, and pelagic communities such as divers (equipped or not with imagery tools) and ROVs. Examples of feedback include: “Different sediments result in different degrees of penetration” [46]; “13 photos were invalidated due to the seabed surface being invisible as the prism had protruded too deep” [47]; “Fish behavior may be affected by the presence of divers” [48]; and “Real-time positioning is a major challenge for micro-ROVs (can be added for a substantial cost)” [49]. Often, the feedback was relative to a specific use for a particular goal (e.g., ROV tether too short to cover the entire survey area when deploying from a drilling platform [50]), but sometimes it was more general such as sled and towed cameras are particularly sensitive to the rocking motion of swell at the surface (e.g., [51,52]), depth is a limit for sampling with scuba divers (e.g., [53]), or corers and grabs do not perform well in coarse sediments (e.g., [12]).
Paired with the abundant diversity of technologies identified in this review, a great variety of analyses and software was used to extract, process, and analyze the data after sampling (Table 4). Some of the software used were proprietary to specific instruments, but the most common ones were PRIMER (75 entries) and R (28 entries). Several studies used the biotic and abiotic data to generate habitat classifications such as the Coastal and Marine Ecological Classification Standard (CMECS; e.g., in [54] or [55]) or the JNCC’s Marine Habitat Classification for Britain and Ireland ([56]; e.g., in [57] or [58]). However, the most common analyses were univariate (e.g., ANOVA) or multivariate statistical analyses (e.g., (n)MDS, PCA, PERMANOVA, SIMPER) aimed at calculating and comparing biodiversity indices, characterizing faunal assemblages or sediment classes, or modeling the distribution of animals related to abiotic parameters (Table 4).

4. Discussion

As one would expect with such a broad research field, the diversity of technologies available for characterizing and measuring changes in benthic and pelagic habitats is considerable, making the development of recommendations for technologies and sampling methods that fulfill the monitoring needs around marine energy project sites challenging. As was often emphasized in the feedback from the authors of the documents reviewed here, many technologies are susceptible to excessive hydrodynamic energy, which is true in many marine environments, but especially at sites favorable to marine energy development that are targeted because of their strong tidal currents and high wave profiles. For example, a study noted that the box trawl they were using was limited to flow velocities below 1.8 m·s−1 [59], while another commented on the interference on their sonar data due to the entrained air in strong tidal currents [60]. Strong currents were also an issue for maintaining ROVs, towed cameras, and even scuba divers at a constant height above the seafloor and along straight transects [36,51,61]. Swell conditions affected the quality of the data obtained by tethered instruments such as ROVs and towed cameras by creating vertical motion that could, sometimes, not be controlled [52,62]. Heavier technologies seemed to be less affected than those of lighter build [63]. Heavy swells and currents also tend to resuspend the sediment and alter the visibility, limiting the use of video and still imagery [36,64,65]. In some areas, the currents are so fierce that they have flushed away the thinner sediments, thereby affecting the ability to use corers or grabs to collect sediment and infauna samples [12]. Despite the diversity of corers and grabs used in the reviewed studies, our examination did not highlight any technology more suitable than others when it comes to sampling coarse sediments and infauna living therein. Nevertheless, if timed properly regarding slack tides and storm swell, all the technologies identified in the present literature review have been and/or would be applicable to marine energy development sites. In addition to the upfront cost of an instrument, an important factor to keep in mind when selecting a technology for marine energy sites is its reliability and durability in harsh conditions, so that the necessary sampling can be obtained without too many trials that add costly ship and labor times to a survey [11].
Table 5 summarizes the applicability to marine energy project sites of the most frequently used technologies for each of the six habitat categories, including noted limitations on the use in high-energy environments, known unwanted impacts on species and/or habitats of interest, cost range of the technologies themselves, and whether the software required for data analysis are proprietary or open source. Table 6 provides recommendations on which technologies to use to survey benthic (epifauna and infauna) and demersal organisms at wave and tidal energy sites. These recommendations are based on a set of criteria related to the main general variables that would guide the selection of a technology: strength of currents, wave height, water depth, presence of obstacles in the water (e.g., marine energy devices, cables), and nature of the seabed. Local specificities and average weather conditions (e.g., wind, swell) also influence the technology selection during a project’s planning process. Many technologies come in various sizes and shapes, and the best options to sustain high-energy environments may be the most adaptable ones, with the possibility to add weights to ballast in the water or on the seafloor, thrusters for extra propulsion, a frame to guide sampling after impact on the seafloor, etc. Reducing the dependence on a tether (e.g., autonomous underwater vehicle vs. ROV) will attenuate the effects from the swell in high wave conditions.
Overall, video and still imagery, and visual surveys in general, seem to be the most common method used for characterizing surface sediments, epifauna, pelagic, and biofouling communities. These technologies are highly adaptable; often deployed as a dropdown system, buoy, platform, or float at different levels of the water column; mounted on ROVs, sleds, or submarines; or held by divers. Depending on the characteristics of a marine energy project site or goals of a study, one technology may be better adapted than another. For instance, Kregting et al. [58] used a drop camera rather than scuba divers because of cost considerations, while O’Carroll et al. [66] used divers equipped with video cameras to survey the seafloor at the foot of a tidal turbine because a drop camera or ROV could not get close enough. Drop cameras are great tools for collecting standardized images of the seafloor and benthic communities (e.g., [58,64]), but are difficult to implement when looking forward at a specific target, for example, to assess colonization and the reef effect around moorings and foundations. Using a 360-degree camera would assure that the target is in the field of view, as long as water turbidity allows for good visibility [67]. Divers are usually more suitable in dense kelp fields or close to/underneath artificial structures (e.g., [68,69]), but both divers and underwater vehicles are known to potentially affect the behavior of marine animals during surveys (e.g., [70,71]). Imagery technologies mounted on robotics or drop frames have the advantage of achieving greater depths with longer bottom times than diver surveys [72,73,74]. Drop, sled, or towed cameras are often highly customizable; some are equipped with multiple cameras facing different angles and with other instruments such as a conductivity–temperature–depth sensor (e.g., [52]), while others are built to endure strong currents and navigate rugged terrains (e.g., [75,76]).
Often, technologies are used in pairs (simultaneously or not), either to add a layer of data collection or to ground-truth the results obtained with another instrument. Corers, grabs, and drop cameras are common technologies for ground-truthing side-scan sonar and multibeam echosounder data when mapping seafloor and sediment characteristics (e.g., [64]); trawls can be used to ground-truth demersal fish communities described using hydroacoustic methods (e.g., [77]); and scuba diver and/or beam trawl surveys have been used to ground-truth epifaunal assemblages characterized from data collected by ROVs, towed cameras, or video sleds (e.g., [78]). Ground-truthing using an independent technology is particularly important when environmental conditions make sampling challenging. As an alternative to using two truly independent technologies that would require extra ship and labor costs, modifying an existing instrument to pair it with a second technology may prove sufficient. For instance, adding a video camera to a beam trawl is a common way to obtain images of both sessile and mobile epifauna and demersal fauna that are not well sampled with a trawl such as sea pens or other sessile organisms able to quickly retract into the sediment, or fast-moving fishes and invertebrates fleeing the approaching trawl (e.g., [79]). Others have modified sediment grabs by mounting a camera in a waterproof housing to the side of the grab and doubling it as a drop camera to obtain still or video imagery of the sediment surface and epifauna (e.g., [17,80]). Similarly, some SPIs come equipped with a plan view camera, which greatly improves the identification and enumeration of epifauna compared to what is visible on the prism image only [81,82].
However, the choice of sampling designs and statistical analyses may be as important as (if not more important than) the technologies for identifying and measuring changes in habitats [18,19]. Sampling designs such as BACI that involve a comparison of prior- and post-disturbance states, or between affected and control sites are broadly used for assessing impacts, but need to rely on good baseline or reference data [83]. However, if changes in habitats caused by marine energy devices are to be identified and measured, baseline and reference data need to be obtained prior to site disturbance, stored as raw data and, as much as possible, made available publicly for future comparisons with post-disturbance surveys [12]. Gradient designs are other suitable options that do not require baseline or historical data, in the sense that the sampling measures how effects decrease with increasing distance from the source of disturbance, thereby providing a spatial understanding of the impact [84,85]. A before-after-gradient design adds a temporal scale, especially if the sampling is repeated over multiple seasons and years [86,87]. When available, seafloor baseline assessments are often used to inform stratified and gradient sampling designs, identifying different substrata where sampling needs to take place in order to characterize the various biotopes (e.g., [88,89,90]). Once data were collected, parameters assessed to characterize infauna, epifauna, pelagic, and biofouling communities in the studies here reviewed were highly diverse, including measurements of diversity (e.g., Shannon–Wiener’s, Shannon–Weaver’s, Chao’s, Simpson’s), abundance, biomass, species richness, species evenness, and percent cover. Various multivariate statistical analyses were then used to identify differences in assemblages and/or spatiotemporal changes in habitats. Depending on the objectives of a study, these parameters were further converted into biodiversity or habitat quality indices (e.g., AZTI Marine Biotic index in Umehara et al. [91], Benthic Habitat Quality index in Rosenberg et al. [46], or Bottom Association index in Degraer et al. [92]).

5. Conclusions

In conclusion, the high diversity of marine habitats and technologies already used to survey them preclude recommending a specific set of technologies for characterizing changes in benthic and pelagic habitats caused by marine energy devices. However, technologies and sampling methods that are adaptable and designed for working efficiently in energetic environments should be favored, alongside sampling designs and statistical analyses carefully thought out to identify differences in faunal assemblages and spatiotemporal changes in habitats. Because several national and international guidelines for sampling and monitoring benthic and pelagic habitats around offshore activities already exist, relying on these existing guidelines is recommended when selecting suitable monitoring technologies, sampling designs, and sets of data analyses. More importantly for monitoring reports and publications is the need to thoroughly describe the reasons why a specific technology was selected, the methods employed to implement the technology in the field, the sampling design followed to collect data, the data processing and analyzing steps, and any benefits or drawbacks the technology provided to the study. Publicly sharing this information with the marine energy community will help progress toward more transparency and consistency in data collection, and enable the transferability of data and results among projects to fulfill environmental permitting requirements and lower the costs associated with baseline characterizations and post-installation monitoring surveys.

Author Contributions

Conceptualization, L.G.H.; Methodology, L.G.H.; Formal analysis, L.G.H., K.F.M. and L.G.T.; Writing—original draft preparation, L.G.H. and K.F.M.; Writing—review and editing, L.G.H., K.F.M. and L.G.T.; Visualization, K.F.M. All authors have read and agreed to the published version of the manuscript.

Funding

This research was possible due to the generous support of the U.S. Department of Energy EERE Water Power Technologies Office (WPTO) to Pacific Northwest National Laboratory (PNNL) under contract DE-AC05-76RL01830.

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

Not applicable.

Acknowledgments

We are grateful for the ongoing support and guidance from PNNL staff with the Triton Initiative, including Alicia Amerson and Joe Haxel. We thank Samantha Eaves of WPTO for the helpful feedback and Susan Ennor of PNNL for assistance with the manuscript.

Conflicts of Interest

The authors declare no conflict of interest. The funders had no role in the design of the study; in the collection, analyses, or interpretation of data; in the writing of the manuscript, or in the decision to publish the results.

Appendix A

Appendix A compiles the citations of all 259 documents used for the present literature review, listed in alphabetical order.
  • AECOM Canada Ltd. (2009). Environmental assessment registration document—Fundy Tidal Energy Demonstration Project—Volume I: environmental assessment. Halifax, NS, Canada: p 247.
  • AECOM Canada Ltd. (2010). Fundy Ocean Research Centre for Energy (FORCE) environmental assessment addendum to the report: environmental assessment registration document—Fundy Tidal Energy Demonstration Project, Volumes 1 and 2 dated 10 June 2009. Halifax, NS, Canada: p. 52.
  • Ajemian, M. J., J. J. Wetz, B. Shipley-Lozano and G. W. Stunz (2015). Rapid assessment of fish communities on submerged oil and gas platform reefs using remotely operated vehicles. Fisheries Research, 167: 143–155.
  • Alcorn, R., E. Amon, S. Armstrong, B. Batten, D. Bull, B. Cahill, E. Cotilla-Sanchez, G. Dalton, D. Hellin, S. Henkel, A. Husky, J. Klure, B. Langley, B. Polagye, J. Rea, M. Sanders, A. Stewart, G. Sutton and J. Weber (2017). The Pacific Marine Energy Center South Energy Test Site (PMEC-SETS) final report: final site selection, preliminary facility design, and cost & schedule estimates. Pacific Marine Energy Center (PMEC): p. 604.
  • Andaloro, F., M. Ferraro, E. Mostarda, T. Romeo and P. Consoli (2013). Assessing the suitability of a remotely operated vehicle (ROV) to study the fish community associated with offshore gas platforms in the Ionian Sea: a comparative analysis with underwater visual censuses (UVCs). Helgoland Marine Research, 67(2): 241–250.
  • Andersen, K., A. Chapman, N. Hareide, A. Folkestad, E. Sparrevik and O. Langhamer (2009). Environmental monitoring at the Maren Wave Power Test Site off the Island of Runde, Western Norway: planning and design. 8th European Wave and Tidal Energy Conference, Uppsala, Sweden.
  • Aquafact International Services Ltd. (2010). Marine environmental appraisal of an ocean energy test site in Inner Galway Bay. Galway, Ireland: p. 51.
  • Aquatera Ltd. (2011). Environmental monitoring report—2011 installation of monopile at Voith Hydro test berth, Fall of Warness, Orkney Report. Heidenheim, Germany: p. 39.
  • Aquatera Ltd. (2015). SSF Scapa Flow sites benthic ROV survey St Margaret’s Hope. Stromness, Orkney, UK: p. 26.
  • Argyll Tidal Limited (2013). Environmental appraisal (EA) for the Argyll Tidal Demonstrator Project. Nautricity: p. 207.
  • Atkins Portugal (2014). Environmental characterisation study of the ENONDAS S.A. pilot zone—executive summary. Lisbon, Portugal: p. 30.
  • Atlantic Marine Geological Consulting Ltd. (2009). Geological report for the proposed in stream tidal power demonstration project in Minas Passage, Bay of Fundy, Nova Scotia. Appendix 3: geology, bathymetry, ice and seismic conditions. Hantsport, NS, Canada: p. 76.
  • Bacouillard, L., N. Baux, J. C. Dauvin, N. Desroy, K. J. Geiger, F. Gentil and E. Thiebaut (2020). Long-term spatio-temporal changes of the muddy fine sand benthic community of the Bay of Seine (eastern English Channel). Marine Environmental Research, 161: 105062.
  • Bald, J., A. del Campo, J. Franco, I. Galparsoro, M. Gonzalez, C. Hernandez, P. Liria, I. Menchaca, I. Muxika, O. Solaun, A. Uriarte, Y. Torre Encisco and D. Marina (2015). The Environmental impact study of the Biscay Marine Energy Platform (BIMEP) project. Marine Energy Week. Bilbao, Spain.
  • Bald, J., A. del Campo, J. Franco, I. Galparsoro, M. González, C. Hernández, P. Liria, I. Menchaca, I. Muxika, O. Solaun, A. Uriarte and M. Uyarra (2012). The Biskay Marine Energy Platform (BIMEP), environmental impacts and monitoring plan. 4th International Conference on Ocean Energy. Dublin, Ireland: p. 6.
  • Bald, J., J. Franco, I. Menchaca, Y. Torre Encisco and D. Marina (2017). Impact on seabirds of new offshore wind energy test and demonstration projects in the Biscay Marine Energy Platform (BiMEP, N. Spain). Marine Energy Week. Bilbao, Spain.
  • Bald, J., I. Galparsoro, M. González, C. Hernandez, P. Liria, J. Mader, I. Muxika, I. Adarraga, I. Cruz, M. Markiegui, J. Martinez, J. Maria Ruiz, Y. Torre Encisco and D. Marina (2015). The Biscay Marine Energy Platform (BIMEP) preoperational environmental monitoring plan. Marine Energy Week. Bilbao, Spain.
  • Bald, J., C. Hernandez, I. Galparsoro, J. Rodriguez, I. Muxika, I. Cruz, M. Markiegui, J. Martinez, J. Maria Ruiz, Y. Torre Encisco and D. Marina (2015). Environmental impacts over the seabed and benthic communities of submarine cable installation in the Biscay Marine Energy Platform (bimep). Marine Energy Week. Bilbao, Spain.
  • Bald, J., C. Hernandez, I. Galparsoro, J. Rodriguez, I. Muxika, Y. Torre Encisco and D. Marina (2014). Environmental impacts over the seabed and benthic communities of underwater cable installation in the Biscay Marine Energy Platform (BIMEP). EIMR International Conference, Stornoway, UK.
  • Bald, J., C. Hernandez, A. Uriarte, J. Antonio Castillo, P. Ruiz, N. Ortega, Y. Torre Encisco and D. Marina (2015). Acoustic characterization of submarine cable installation in the Biscay Marine Energy Platform (bimep. Marine Energy Week. Bilbao, Spain.
  • Barrie, J. V. and K. W. Conway (2014). Seabed characterization for the development of marine renewable energy on the Pacific margin of Canada. Continental Shelf Research, 83: 45–52.
  • Batten, B. (2014). Northwest National Marine Renewable Energy Center at Oregon State University Pacific Marine Energy Center South Energy Test Site scoping document 2. Corvallis, OR, USA: p. 147.
  • Bender, A., O. Langhamer and J. Sundberg (2020). Colonisation of wave power foundations by mobile mega- and macrofauna—A 12 year study. Marine Environmental Research, 161: 105053.
  • Bender, A. and J. Sundberg (2018). Effects of wave energy generators on Nephrops norvegicus. 4th Asian Wave and Tidal Energy Conference (AWTEC), Taipei, Taiwan.
  • Bibby HydroMap (2015). Deep Green project and export cable route—Offshore survey. Volume 1—Operation Report. London, UK: p. 126.
  • Bicknell, A. W. J., B. J. Godley, E. V. Sheehan, S. C. Votier and M. J. Witt (2016). Camera technology for monitoring marine biodiversity and human impact. Frontiers in Ecology and the Environment, 14(8): 424–432.
  • Birchenough, S. N. R., S. G. Bolam and R. E. Parker (2013). SPI-ing on the seafloor: characterising benthic systems with traditional and in situ observations. Biogeochemistry, 113: 105–117.
  • Birchenough, S. N. R., S. E. Boyd, R. A. Coggan, D. S. Limpenny, W. J. Meadows and H. L. Rees (2006). Lights, camera and acoustics: Assessing macrobenthic communities at a dredged material disposal site off the North East coast of the UK. Journal of Marine Systems, 62(3–4): 204–216.
  • BMT Oceanica Pty Ltd. (2015). CETO 6 Garden Island marine environmental management plan. Wembley, Australia: p. 360.
  • BMT Oceanica Pty Ltd. (2016). CETO 6 Garden Island project state referral form. Wembley, Australia: p. 56.
  • Bond, T., J. Prince, D. L. McLean and J. C. Partridge (2020). Comparing the utility of industry ROV and hybrid-AUV imagery for surveys of fish along a subsea pipeline. Marine Technology Society Journal, 54(3): 33–42.
  • BioPower Systems Pty Ltd. (2016). The Port Fairy pilot wave energy project environmental management plan version 2.2. Sydney, Australia: p. 38.
  • Broadhurst, M., S. Barr and C. D. L. Orme (2014). In-situ ecological interactions with a deployed tidal energy device; an observational pilot study. Ocean & Coastal Management, 99: 31–38.
  • Broadhurst, M. and C. D. Orme (2014). Spatial and temporal benthic species assemblage responses with a deployed marine tidal energy device: a small scaled study. Marine Environmental Research, 99: 76–84.
  • Callaway, R. (2016). Historical data reveal 30-year persistence of benthic fauna associations in heavily modified waterbody. Frontiers in Marine Science, 3: 13.
  • Carey, D. A., M. Hayn, J. D. Germano, D. I. Little, and B. Bullimore (2015). Marine habitat mapping of the Milford Haven Waterway, Wales, UK: Comparison of facies mapping and EUNIS classification for monitoring sediment habitats in an industrialized estuary. Journal of Sea Research, 100: 99–119.
  • Carl Bro Group Ltd. (2002). Marine Energy Test Center environmental statement. Glasgow, UK: p. 57.
  • Carlier, A., X. Caisey, J. Gaffet, M. Lejart, S. Derrien-Courtel, E. Catherine, E. Quimbert, and O. Soubigou (2014). Monitoring benthic habitats and biodiversity at the tidal energy site of Paimpol-Brehat (Brittany, France). Proceedings of the 2nd International Conference on Environmental Interactions of Marine Renewable Energy Technologies (EIMR2014), Stornoway, Scotland, UK.
  • CEF Consultants Ltd. (2010). Fundy Tidal Energy Demonstration Project lobster catch monitoring: analysis of results from two fall surveys: September 25–October 3 and November 5—18, 2009. Hantsport, Nova Scotia, Canada: p. 44.
  • Claisse, J. T., M. S. Love, E. L. Meyer-Gutbrod, C. M. Williams and D. J. Pondella II (2019). Fishes with high reproductive output potential on California offshore oil and gas platforms. Bulletin of Marine Science, 95(4): 515–534.
  • Centre for Marine and Coastal Studies Ltd. (CMACS) (2015). Deep Green project Holyhead Deep benthic technical report, CMACS. Eastham, UK: p. 106.
  • Coates, D. A., Y. Deschutter, M. Vincx and J. Vanaverbeke (2014). Enrichment and shifts in macrobenthic assemblages in an offshore wind farm area in the Belgian part of the North Sea. Marine Environmental Research, 95: 1–12.
  • Cochrane, G. R., L. G. Hemery and S. K. Henkel (2017). Oregon OCS seafloor mapping: Selected lease blocks relevant to renewable energy. U.S. Geological Survey Open-File Report 2017-1045 and Bureau of Ocean Energy Management OCS Study BOEM 2017-018: p. 57.
  • Cochrane, S. K. J., T. H. Pearson, M. Greenacre, J. Costelloe, I. H. Ellingsen, S. Dahle and B. Gulliksen (2012). Benthic fauna and functional traits along a Polar Front transect in the Barents Sea—Advancing tools for ecosystem-scale assessments. Journal of Marine Systems, 94: 204–217.
  • Cooper, L. W., M. L. Guarinello, J. M. Grebmeier, A. Bayard, J. R. Lovvorn, C. A. North and J. M. Kolts (2019). A video seafloor survey of epibenthic communities in the Pacific Arctic including Distributed Biological Observatory stations in the northern Bering and Chukchi seas. Deep Sea Research Part II: Topical Studies in Oceanography, 162: 164–179.
  • Cordier, T., F. Frontalini, K. Cermakova, L. Apotheloz-Perret-Gentil, M. Treglia, E. Scantamburlo, V. Bonamin and J. Pawlowski (2019). Multi-marker eDNA metabarcoding survey to assess the environmental impact of three offshore gas platforms in the North Adriatic Sea (Italy). Marine Environmental Research, 146: 24–34.
  • Cossu, R., C. Heatherington, I. Penesis, R. Beecroft and S. Hunter (2020). Seafloor site characterization for a remote island OWC device near King Island, Tasmania, Australia. Journal of Marine Science and Engineering, 8: 13.
  • Cruz-Marrero, W., D. W. Cullen, N. R. Gay and B. G. Stevens (2019). Characterizing the benthic community in Maryland’s offshore wind energy areas using a towed camera sled: Developing a method to reduce the effort of image analysis and community description. PLoS ONE, 14(5): e0215966.
  • Culha, M., H. Somek and O. Aksoy (2019). Impact of offshore aquaculture on molluscan biodiversity in Ildir Bay, Aegean Sea, Turkey. Journal of Environmental Biology, 40: 76–83.
  • Currie, D. R. and L. R. Isaacs (2005). Impact of exploratory offshore drilling on benthic communities in the Minerva gas field, Port Campbell, Australia. Marine Environmental Research, 59(3): 217–233.
  • Davies, B. F. R., M. J. Attrill, L. Holmes, A. Rees, M. J. Witt and E. V. Sheehan (2020). Acoustic Complexity Index to assess benthic biodiversity of a partially protected area in the southwest of the UK. Ecological Indicators, 111.
  • Davison, A. and T. Mallows (2005). Strangford Lough marine current turbine environmental statement final report. Edinburgh, Scotland, UK: p. 141.
  • De Backer, A., G. Van Hoey, D. Coates, J. Vanaverbeke and K. Hostens (2014). Similar diversity-disturbance responses to different physical impacts: three cases of small-scale biodiversity increase in the Belgian part of the North Sea. Marine Pollution Bulletin, 84: 251–262.
  • Degraer, S., R. Brabant, B. Rumes, L. Vigin and (eds.) (2019). Environmental impacts of offshore wind farms in the Belgian part of the North Sea: marking a decade of monitoring, research and innovation. Brussels, Belgium: p. 134.
  • Dempster, T., P. Sanchez-Jerez, J. T. Bayle-Sempere, F. Gimenez-Casalduero and C. Valle (2002). Attraction of wild fish to sea-cage fish farms in the south-western Mediterranean Sea: spatial and short-term temporal variability. Marine Ecology Progress Series, 242: 237–252.
  • Devine Tarbell & Associates (2006). Roosevelt Island Tidal Energy Project (FERC No. 12611) study plans. Syracuse, NY, USA: p. 97.
  • Diaz, R. J., G. R. Cutter and D. M. Dauer (2003). A comparison of two methods for estimating the status of benthic habitat quality in the Virginia Chesapeake Bay. Journal of Experimental Marine Biology and Ecology, 285–286: 371–381.
  • Doray, M., E. Josse, P. Gervain, L. Reynal and J. Chantrel (2007). Joint use of echosounding, fishing and video techniques to assess the structure of fish aggregations around moored Fish Aggregating Devices in Martinique (Lesser Antilles). Aquatic Living Resources, 20(4): 357–366.
  • DP Energy Ireland Ltd. (2014). Fair Head Tidal Energy Park consent application—Appendices. Volume 4. Belfast, Northern Ireland, UK: p. 1269.
  • Dunham, A., J. R. Pegg, W. Carolsfeld, S. Davies, I. Murfitt and J. Boutillier (2015). Effects of submarine power transmission cables on a glass sponge reef and associated megafaunal community. Marine Environmental Research, 107: 50–60.
  • Eerkes-Medrano, D., J. Drewery, F. Burns, P. Cárdenas, M. Taite, D. W. McKay, D. Stirling and F. Neat (2020). A community assessment of the demersal fish and benthic invertebrates of the Rosemary Bank Seamount marine protected area (NE Atlantic). Deep Sea Research Part I: Oceanographic Research Papers, 156: 103180.
  • Envirosphere Consultants Limited (2009). Appendix 4: Benthic communities—seabed biological communities in the Minas Passage. Environmental assessment registration document—Fundy Tidal Energy Demonstration Project Volume I: Environmental Assessment. AECOM. Hantsport, Nova Scotia, Canada: p. 56.
  • European Marine Energy Centre (2011). Scapa Flow Scale Site: Environmental description. Stromness, Orkney, UK: p. 35.
  • European Marine Energy Centre (2014). EMEC Fall of Warness Test Site: Environmental appraisal. REP 443-04-01 20141120. Stromness, Orkney, UK: p. 326.
  • European Marine Energy Centre (2019). Scapa Flow Scale Test Site: Environmental description. Stromness, Orkney, UK: p. 47.
  • FaB Test (2014). FaB Test: Falmouth Bay Test Site marine renewables commissioning site guide to deployments & application process requirements. Exeter, UK: p. 23.
  • Fields, S., S. Henkel and G. C. Roegner (2019). Video sleds effectively survey epibenthic communities at dredged material disposal sites. Environmental Monitoring and Assessment, 191(6): 404.
  • Foubister, L. (2005). EMEC Tidal Test Facility Fall of Warness Eday, Orkney: Environmental statement. Stromness, Orkney, UK: p. 176.
  • Fujii, T. (2015). Temporal variation in environmental conditions and the structure of fish assemblages around an offshore oil platform in the North Sea. Marine Environmental Research, 108: 69–82.
  • Gates, A. R., T. Horton, A. Serpell-Stevens, C. Chandler, L. J. Grange, K. Robert, A. Bevan and D. O. B. Jones (2019). Ecological role of an offshore industry artificial structure. Frontiers in Marine Science, 6: 675.
  • Germano, J. D., D. C. Rhoads, R. M. Valente, D. A. Carey and M. Solan (2011). The use of sediment profile imaging (SPI) for environmental impact assessments and monitoring studies: Lessons learned from the past four decades. Oceanography and Marine Biology: An Annual Review, 49: 235–297.
  • Goldfinger, C., S. Henkel, C. Romsos, A. Havron and B. Black (2014). Benthic habitat characterization offshore the Pacific Northwest—Volume 1: Evaluation of continental shelf geology. US Department of the Interior, Bureau of Ocean Energy Management, Pacific OCS Region, OCS Study BOEM 2014–662: p. 161.
  • Gonzalez, S., J. K. Horne and E. Ward (2019). Temporal variability in pelagic biomass distributions at wave and tidal sites and implications for standardization of biological monitoring. International Marine Energy Journal, 2(1): 15–28.
  • Greene, H. G. (2015). Habitat characterization of a tidal energy site using an ROV: Overcoming difficulties in a harsh environment. Continental Shelf Research, 106: 85–96.
  • Griffin, R. A., R. E. Jones, N. E. L. Lough, C. P. Lindenbaum, M. C. Alvarez, K. A. J. Clark, J. D. Griffiths and P. A. T. Clabburn (2020). Effectiveness of acoustic cameras as tools for assessing biogenic structures formed by Sabellaria in highly turbid environments. Aquatic Conservation: Marine and Freshwater Ecosystems, 30(6): 1121–1136.
  • Guarinello, M. L. and D. A. Carey (2020). Multi-modal approach for benthic impact assessments in moraine habitats: a case study at the Block Island wind farm. Estuaries and Coasts: 1–16.
  • Guida, V., A. Drohan, H. Welch, J. McHenry, D. Johnson, V. Kentner, J. Brink, D. Timmons, J. Pessutti, S. Fromm and E. Estela-Gomez (2017). Habitat mapping and assessment of northeast wind energy areas. US Department of Interior, Bureau of Ocean Energy Management, Office of Renewable Energy Programs, OCS Study BOEM 2017-088: p. 312.
  • Halcrow Group Limited (2006). South West of England regional development agency Wave Hub environmental statement. South West of England Regional Development Agency, Exeter, UK: p. 278.
  • Hayes, P. and N. C. Lacey (2019). Epifauna associated with subsea pipelines in the North Sea. ICES Journal of Marine Science, 77(3): 1137–1147.
  • HDR (2018). Benthic monitoring during wind turbine installation and operation at the Block Island wind farm, Rhode Island. U.S. Department of the Interior, Bureau of Ocean Energy Management, Office of Renewable Energy Programs, OCS Study BOEM 2018-047: p. 155.
  • HDR (2020). Benthic and epifaunal monitoring during wind turbine installation and operation at the Block Island wind farm, Rhode Island—Project Report. Volumes 1 & 2. U.S. Department of the Interior, Bureau of Ocean Energy Management, Office of Renewable Energy Programs, OCS Study BOEM 2020-044: p. 263.
  • Hemery, L. G., S. K. Henkel and G. R. Cochrane (2018). Benthic assemblages of mega epifauna on the Oregon continental margin. Continental Shelf Research, 159: 24–32.
  • Hemery, L. G., K. K. Politano and S. K. Henkel (2017). Assessing differences in macrofaunal assemblages as a factor of sieve mesh size, distance between samples, and time of sampling. Environmental Monitoring and Assessment, 189: 413.
  • Henkel, S. (2016). Assessment of benthic effects of anchor presence and removal. Northwest National Marine Renewable Energy Center (NNMREC), Corvallis, OR, USA: p. 22.
  • Henkel, S., C. Goldfinger, C. Romsos, L. Hemery, A. Havron and K. Politano (2014). Benthic habitat characterization offshore the Pacific Northwest—Volume 2: Evaluation of continental shelf benthic communities. US Department of the Interior, Bureau of Ocean Energy Management, Pacific OCS Region, BOEM 2014-662: p. 218.
  • Holte, B. and L. Buhl-Mortensen (2020). Does grab size influence sampled macrofauna composition? A test conducted on deep-sea communities in the northeast Atlantic. Marine Environmental Research, 154: 104867.
  • Horne, J., D. Jacques, S. Parker-Stetter, H. Linder and J. Nomura (2013). Evaluating acoustic technologies to monitor aquatic organisms at renewable energy sites final report. U.S. Department of the Interior, Bureau of Ocean Energy Management, BOEM 2014-057: p. 102.
  • Hyland, J., D. Hardin, M. Steinhauer, D. Coats, R. Green and J. Neff (1994). Environmental impact of offshore oil development on the outer continental shelf and slope off Point Arguello, California. Marine Environmental Research, 37(2): 195–229.
  • Ingram, E. C., R. M. Cerrato, K. J. Dunton and M. G. Frisk (2019). Endangered Atlantic sturgeon in the New York wind energy area: Implications of future development in an offshore wind energy site. Scientific Reports, 9: 12432.
  • Insight Marine Projects (2014). FaBTest geophysical survey: Report of survey. University of Exeter, REP-0191/J64567: p. 57.
  • Integral Consulting (2017). Benthic habitat mapping field and data report Sequim Bay April/May 2017: Standardized and cost-effective benthic habitat mapping and monitoring tools for MHK environmental assessments. U.S. Department of Energy (DOE) Office of Energy Efficiency and Renewable Energy (EERE), DE-EE007826: p. 318.
  • Integral Consulting (2017). Environmental monitoring program report 2 results of phases I–IV. Shell Exploration & Production Company, Anchorage, AK, USA: p. 410.
  • Integral Consulting (2019). Benthic habitat mapping field and data report PacWave June 2019: Standardized and cost-effective benthic habitat mapping and monitoring tools for MHK environmental assessments. US Department of Energy (DOE) Office of Energy Efficiency and Renewable Energy (EERE), DE-EE007826: p. 281.
  • Jarvis, S., J. Allen, N. Proctor, A. Crossfield, O. Dawes, A. Leighton, L. McNeill and W. Musk (2004). North Sea wind farms NSW lot 1 benthic fauna. Institute of Estuarine and Coastal Studies (IECS), ZBB607.2-F-2004: p. 91.
  • Kahn, A. S., C. W. Pennelly, P. R. McGill and S. P. Leys (2020). Behaviors of sessile benthic animals in the abyssal northeast Pacific Ocean. Deep Sea Research Part II: Topical Studies in Oceanography, 173: 104729.
  • Keenan, G., C. Sparling, H. Williams and F. Fortune (2011). SeaGen environmental monitoring programme final report. Royal Haskoning, Edinburgh, Scotland, UK: p. 81.
  • Kregting, L., B. Elsaesser, R. Kennedy, D. Smyth, J. O’Carroll and G. Savidge (2016). Do changes in current flow as a result of arrays of tidal turbines have an effect on benthic communities? PLoS ONE, 11(8): e0161279.
  • Kregting, L., P. Schmitt, L. Lieber, R. Culloch, N. Horne and D. Smyth (2018). Environmental impact report of the H2020 project PowerKite. Queen’s University Belfast, Northern Ireland, UK: p. 30.
  • Krone, R., L. Gutow, T. J. Joschko and A. Schroder (2013). Epifauna dynamics at an offshore foundation—Implications of future wind power farming in the North Sea. Marine Environmental Research, 85: 1–12.
  • LaFrance, M., J. W. King, B. A. Oakley and S. Pratt (2014). A comparison of top-down and bottom-up approaches to benthic habitat mapping to inform offshore wind energy development. Continental Shelf Research, 83: 24–44.
  • Langhamer, O. (2010). Effects of wave energy converters on the surrounding soft-bottom macrofauna (west coast of Sweden). Marine Environmental Research, 69: 374–381.
  • Langhamer, O. and D. Wilhelmsson (2007). Wave power devices as artificial reefs. European Wave and Tidal Energy Conference. Porto, Portugal: p. 8.
  • Langhamer, O. and D. Wilhelmsson (2009). Colonisation of fish and crabs of wave energy foundations and the effects of manufactured holes—A field experiment. Marine Environmental Research, 68(4): 151–157.
  • Langhamer, O., D. Wilhelmsson and J. Engström (2009). Artificial reef effect and fouling impacts on offshore wave power foundations and buoys—A pilot study. Estuarine, Coastal and Shelf Science, 82(3): 426–432.
  • Laroche, O., S. A. Wood, L. A. Tremblay, J. I. Ellis, G. Lear and X. Pochon (2018). A cross-taxa study using environmental DNA/RNA metabarcoding to measure biological impacts of offshore oil and gas drilling and production operations. Marine Pollution Bulletin, 127: 97–107.
  • Leclerc, J. C., F. Viard, E. González Sepúlveda, C. Díaz, J. Neira Hinojosa, K. Pérez Araneda, F. Silva, A. Brante and E. Briski (2019). Habitat type drives the distribution of non-indigenous species in fouling communities regardless of associated maritime traffic. Diversity and Distributions, 26(1): 62–75.
  • Lindeboom, H. J., H. J. Kouwenhoven, M. J. N. Bergman, S. Bouma, S. Brasseur, R. Daan, R. C. Fijn, D. de Haan, S. Dirksen, R. van Hal, R. Hille Ris Lambers, R. ter Hofstede, K. L. Krijgsveld, M. Leopold and M. Scheidat (2011). Short-term ecological effects of an offshore wind farm in the Dutch coastal zone; a compilation. Environmental Research Letters, 6: 035101.
  • Long, S., B. Sparrow-Scinocca, M. E. Blicher, N. Hammeken Arboe, M. Fuhrmann, K. M. Kemp, R. Nygaard, K. Zinglersen and C. Yesson (2020). Identification of a soft coral garden candidate vulnerable marine ecosystem (VME) using video imagery, Davis Strait, West Greenland. Frontiers in Marine Science, 7: 460.
  • Love, M. S., J. T. Claisse and A. Roeper (2019). An analysis of the fish assemblages around 23 oil and gas platforms off California with comparisons with natural habitats. Bulletin of Marine Science, 95(4): 477–514.
  • Love, M. S., L. Kui and J. T. Claisse (2019). The role of jacket complexity in structuring fish assemblages in the midwaters of two California oil and gas platforms. Bulletin of Marine Science, 95(4): 597–616.
  • Love, M. S., M. M. Nishimoto, S. Clark, M. McCrea and A. Scarborough Bull (2017). The organisms living around energized submarine power cables, pipe, and natural sea floor in the inshore waters of Southern California. Bulletin, Southern California Academy of Sciences, 116(2): 61–87.
  • Love, M. S., M. M. Nishimoto, L. Snook and L. Kui (2019). An analysis of the sessile, structure-forming invertebrates living on California oil and gas platforms. Bulletin of Marine Science, 95(4): 583–596.
  • Marine Institute (2015). Galway Bay Marine and Renewable Energy Test Site environmental screening report. Marine Institute, Galway, Ireland: p. 30.
  • Mattila, J. (2012). Ecological impacts of a wave energy converter in Hammarudda, Åland Islands—A preliminary assessment after one year of operation. Abo Akademi University, Turku, Finland: p. 11.
  • Mauffrey, F., T. Cordier, L. Apotheloz-Perret-Gentil, K. Cermakova, T. Merzi, M. Delefosse, P. Blanc and J. Pawlowski (2021). Benthic monitoring of oil and gas offshore platforms in the North Sea using environmental DNA metabarcoding. Molecular Ecology, 30(13): 3007–3022.
  • Mavraki, N., I. De Mesel, S. Degraer, T. Moens and J. Vanaverbeke (2020). Resource niches of co-occurring invertebrate species at an offshore wind turbine indicate a substantial degree of trophic plasticity. Frontiers in Marine Science, 7: 379.
  • McIlvenny, J., D. Tamsett, P. Gillibrand and L. Goddijn-Murphy (2016). On the sediment dynamics in a tidally energetic channel: The Inner Sound, Northern Scotland. Journal of Marine Science and Engineering, 4(2): 31.
  • McIntyre, M. L., D. F. Naar, K. L. Carder, B. T. Donahue, and D. J. Mallinson (2006). Coastal bathymetry from hyperspectral remote sensing data: Comparisons with high resolution multibeam bathymetry. Marine Geophysical Researches, 27(2): 129–136.
  • McLean, D. L., M. D. Taylor, A. Giraldo Ospina and J. C. Partridge (2019). An assessment of fish and marine growth associated with an oil and gas platform jacket using an augmented remotely operated vehicle. Continental Shelf Research, 179: 66–84.
  • McLean, D. L., M. D. Taylor, J. C. Partridge, B. Gibbons, T. J. Langlois, B. E. Malseed, L. D. Smith and T. Bond (2018). Fish and habitats on wellhead infrastructure on the north west shelf of Western Australia. Continental Shelf Research, 164: 10–27.
  • McLean, D. L., B. I. Vaughan, B. E. Malseed and M. D. Taylor (2020). Fish-habitat associations on a subsea pipeline within an Australian Marine Park. Marine Environmental Research, 153: 104813.
  • Mendoza, M. and S. K. Henkel (2017). Benthic effects of artificial structures deployed in a tidal estuary. Plankton & Benthos Research, 12(3): 179–189.
  • Meyer, H. K., E. M. Roberts, H. T. Rapp and A. J. Davies (2019). Spatial patterns of arctic sponge ground fauna and demersal fish are detectable in autonomous underwater vehicle (AUV) imagery. Deep Sea Research Part I: Oceanographic Research Papers, 153: 103137.
  • Meyer-Gutbrod, E. L., L. Kui, M. M. Nishimoto, M. S. Love, D. M. Schroeder and R. J. Miller (2019). Fish densities associated with structural elements of oil and gas platforms in southern California. Bulletin of Marine Science, 95(4): 639–656.
  • Meyer-Gutbrod, E. L., M. S. Love, J. T. Claisse, H. M. Page, D. M. Schroeder and R. J. Miller (2019). Decommissioning impacts on biotic assemblages associated with shell mounds beneath southern California offshore oil and gas platforms. Bulletin of Marine Science, 95(4): 683–701.
  • Meyer-Gutbrod, E. L., M. S. Love, D. M. Schroeder, J. T. Claisse, L. Kui and R. J. Miller (2020). Forecasting the legacy of offshore oil and gas platforms on fish community structure and productivity. Ecological Applications, 30(8): e02185.
  • MeyGen (2011). MeyGen Tidal Energy Project—Phase 1 Non-Technical Summary. MeyGen Limited, London, UK: p. 40.
  • MeyGen (2012). MeyGen Tidal Energy Project Phase 1: Environmental Statement. MeyGen Limited, London, UK: p. 544.
  • Minerex Geophysics Limited (2010). Appendix 5—Belmullet Wave Energy Connection, Belderra Strand County Mayo—Geophysical Survey Report Status. Atlantic Marine Energy Test Site Environmental Impact Statement, Sustainable Energy Authority of Ireland, Dublin, Ireland: p. 26.
  • Minesto (2016). Deep Green Holyhead Deep Project Phase I (0.5 MW)—Environmental Statement. Minesto, L-100194-S14-EIAS-001: p. 487.
  • Mireles, C., C. J. B. Martin and C. G. Lowe (2019). Site fidelity, vertical movement, and habitat use of nearshore reef fishes on offshore petroleum platforms in southern California. Bulletin of Marine Science, 95(4): 657–681.
  • Moore, C. G. (2009). Preliminary assessment of the conservation importance of benthic epifaunal species and habitats of the Pentland Firth and Orkney Islands in relation to the development of renewable energy schemes. Scottish Natural Heritage, Report No. 319: p. 41.
  • Morgan, N. B., S. Goode, E. B. Roark and A. R. Baco (2019). Fine Scale Assemblage Structure of Benthic Invertebrate Megafauna on the North Pacific Seamount Mokumanamana. Frontiers in Marine Science, 6: 715.
  • Nall, C. R., M. L. Schlappy and A. J. Guerin (2017). Characterisation of the biofouling community on a floating wave energy device. Biofouling, 33(5): 379–396.
  • Navarrete, S. A., M. Parragué, N. Osiadacz, F. Rojas, J. Bonicelli, M. Fernández, C. Arboleda-Baena, R. Finke and S. Baldanzi (2020). Susceptibility of Different Materials and Antifouling Coating to Macrofouling Organisms in a High Wave-Energy Environment. Journal of Ocean Technology, 15(1): 72–91.
  • Navarrete, S. A., M. Parragué, N. Osiadacz, F. Rojas, J. Bonicelli, M. Fernández, C. Arboleda-Baena, A. Perez-Matus and R. Finke (2019). Abundance, composition and succession of sessile subtidal assemblages in high wave-energy environments of Central Chile: Temporal and depth variation. Journal of Experimental Marine Biology and Ecology, 512: 51–62.
  • Nishimoto, M. M., L. Washburn, M. S. Love, D. M. Schroeder, B. M. Emery and L. Kui (2019). Timing of juvenile fish settlement at offshore oil platforms coincides with water mass advection into the Santa Barbara Channel, California. Bulletin of Marine Science, 95(4): 559–582.
  • O’Carroll, J. P. J., R. M. Kennedy, A. Creech and G. Savidge (2017). Tidal Energy: The benthic effects of an operational tidal stream turbine. Marine Environmental Research, 129: 277–290.
  • O’Donnell, K. P., R. A. Wahle, M. Bell and M. Dunnington (2007). Spatially referenced trap arrays detect sediment disposal impacts on lobsters and crabs in a New England estuary. Marine Ecology Progress Series, 348: 249–260.
  • O’Reilly, R., R. Kennedy, A. Patterson and B. F. Keegan (2006). Ground truthing sediment profile imagery with traditional benthic survey data along an established disturbance gradient. Journal of Marine Systems, 62(3–4): 189–203.
  • O’Carroll, J. P. J., R. M. Kennedy and G. Savidge (2017). Identifying relevant scales of variability for monitoring epifaunal reef communities at a tidal energy extraction site. Ecological Indicators, 73: 388–397.
  • Oakes, C. T. and D. J. Pondella (2009). The Value of a Net-Cage as a Fish Aggregating Device in Southern California. Journal of the World Aquaculture Society, 40(1): 1–21.
  • Ocean Power Technologies (2010). Reedsport OPT Wave Park Settlement Agreement. FERC Project No. 12711. Ocean Power Technologies, Monroe Township, NJ, USA: p. 263.
  • Ocean Renewable Power Company (ORPC) Maine (2011). Final Pilot License Application Cobscook Bay Tidal Energy Project Appendix B: Safeguard Plans. FERC Project No. 12711. Portland, ME, USA: p. 392.
  • Ocean Renewable Power Company (ORPC) Maine (2014). Cobscook Bay Tidal Energy Project: 2013 Environmental Monitoring Report. FERC Project No. 12711. Portland, ME, USA: p. 502.
  • Ocean Renewable Power Company (ORPC) Maine, (2016). Cobscook Bay Tidal Energy Project: 2015 Environmental Monitoring Report. FERC Project No. 12711. Portland, ME, USA: 65.
  • Oregon State University (2019). Volume II S PacWave South Applicant Prepared Environmental Assessment. FERC PROJECT NO. 14616. Corvallis, OR, USA: p. 330.
  • Oregon State University (OSU) and Northwest national Marine Renewable Energy Center (NNMREC) (2012). Wave Energy Test Project—Final Environmental Assessment. Appendix E, monitoring plans. US Department of Energy (DOE), DOE/EA-1917: p. 18.
  • Page, H. M., J. E. Dugan, D. S. Dugan, J. B. Richards and D. M. Hubbard (1999). Effects of an offshore oil platform on the distribution and abundance of commercially important crab species. Marine Ecology Progress Series, 185: 47–57.
  • Page, H. M., S. F. Zaleski, R. J. Miller, J. E. Dugan, D. M. Schroeder and B. Doheny (2019). Regional patterns in shallow water invertebrate assemblages on offshore oil and gas platforms along the Pacific continental shelf. Bulletin of Marine Science, 95(4): 617–638.
  • Pandian, P. K., J. P. Ruscoe, M. Shields, J. C. Side, R. E. Harris, S. A. Kerr and C. R. Bullen (2009). Seabed habitat mapping techniques: an overview of the performance of various systems. Mediterranean Marine Science, 10(2): 29–43.
  • Patterson, A., R. Kennedy, R. O’Reilly and B. F. Keegan (2006). Field test of a novel, low-cost, scanner-based sediment profile imaging camera. Limnology and Oceanography: Methods, 4: 30–37.
  • Pattison, L., A. Serrick and C. Brown (2020). Testing 360 degree imaging technologies for improved animal detection around tidal energy installations. Offshore Energy Research Association of Nova Scotia (OERA), Halifax, NS, Canada: p. 97.
  • Pearce, B., J. M. Fariñas-Franco, C. Wilson, J. Pitts, A. deBurgh and P. J. Somerfield (2014). Repeated mapping of reefs constructed by Sabellaria spinulosa Leuckart 1849 at an offshore wind farm site. Continental Shelf Research, 83: 3–13.
  • Plumlee, J. D., K. M. Dance, M. A. Dance, J. R. Rooker, T. C. TinHan, J. B. Shipley and R. J. D. Wells (2020). Fish assemblages associated with artificial reefs assessed using multiple gear types in the northwest Gulf of Mexico. Bulletin of Marine Science, 96(4): 655–678.
  • Public Utility District No. 1 of Snohomish County (2012). Admiralty Inlet Pilot Tidal Project: Benthic Habitat Monitoring Plan. FERC Project No. 12690, Snohomish, WA, USA: p. 14.
  • Public Utility District No. 1 of Snohomish County (2013). Admiralty Inlet Final Environmental Assessment. Report No. 20130809-3010. FERC Project No. 12690-005, Snohomish, WA, USA: p. 248.
  • Punzo, E., P. Strafella, G. Scarcella, A. Spagnolo, A. M. De Biasi and G. Fabi (2015). Trophic structure of polychaetes around an offshore gas platform. Marine Pollution Bulletin, 99(1–2): 119–125.
  • Raineault, N. A., A. C. Trembanis, D. C. Miller and V. Capone (2013). Interannual changes in seafloor surficial geology at an artificial reef site on the inner continental shelf. Continental Shelf Research, 58: 67–78.
  • Ramalho, S. P., L. Lins, K. Soetaert, N. Lampadariou, M. R. Cunha, A. Vanreusel and E. Pape (2020). Ecosystem Functioning Under the Influence of Bottom-Trawling Disturbance: An Experimental Approach and Field Observations from a Continental Slope Area in the West Iberian Margin. Frontiers in Marine Science, 7: 457.
  • Raoult, V., L. Tosetto, C. Harvey, T. M. Nelson, J. Reed, A. Parikh, A. J. Chan, T. M. Smith and J. E. Williamson (2020). Remotely operated vehicles as alternatives to snorkellers for video-based marine research. Journal of Experimental Marine Biology and Ecology, 522: 151253.
  • Rassweiler, A., A. K. Dubel, G. Hernan, D. J. Kushner, J. E. Caselle, J. L. Sprague, L. Kui, T. Lamy, S. E. Lester and R. J. Miller (2020). Roving Divers Surveying Fish in Fixed Areas Capture Similar Patterns in Biogeography but Different Estimates of Density When Compared With Belt Transects. Frontiers in Marine Science, 7: 272.
  • Reedsport OPT Wave Park, L. (2010). Reedsport OPT Wave Park Settlement Agreement Appendices and Exhibits. Volume IV. FERC Project No. 12713. Reedsport, OR, USA: p. 223.
  • Reubens, J. T., S. Degraer and M. Vincx (2011). Aggregation and feeding behaviour of pouting (Trisopterus luscus) at wind turbines in the Belgian part of the North Sea. Fisheries Research, 108: 223–227.
  • Revelas, E. C., C. Jones, B. Sackmann and N. Maher (2020). A Benthic habitat monitoring approach for marine and hydrokinetic sites: Standardized and cost-effective benthic habitat mapping and monitoring tools for MHK environmental assessments. US Department of Energy (DOE) Office of Energy Efficiency and Renewable Energy (EERE), DE-EE007826: p. 178.
  • Rhodes, N., T. Wilms, H. Baktoft, G. Ramm, J. L. Bertelsen, H. Flávio, J. G. Støttrup, B. M. Kruse and J. C. Svendsen (2020). Comparing methodologies in marine habitat monitoring research: An assessment of species-habitat relationships as revealed by baited and unbaited remote underwater video systems. Journal of Experimental Marine Biology and Ecology, 526: 151315.
  • Robertson, C. M., A. W. J. Demopoulos, J. R. Bourque, F. Mienis, G. C. A. Duineveld, M. S. S. Lavaleye, R. K. K. Koivisto, S. D. Brooke, S. W. Ross, M. Rhode and A. J. Davies (2020). Submarine canyons influence macrofaunal diversity and density patterns in the deep-sea benthos. Deep Sea Research Part I: Oceanographic Research Papers, 159: 103249.
  • Rollings, E. D., C. Eastham, C. (2016). MeyGen Tidal Energy Project Phase 1 Project Environmental Monitoring Programme. MEY-1A-70-HSE-018-I-PEMP. MeyGen Limited, London, UK: p. 201.
  • Romano, E., M. C. Magno and L. Bergamin (2018). Grain size of marine sediments in the environmental studies, from sampling to measuring and classifying. A critical review of the most used procedures. Acta IMEKO, 7(2): 10–15.
  • Rosenberg, R., M. Magnusson and H. C. Nilsson (2009). Temporal and spatial changes in marine benthic habitats in relation to the EU Water Framework Directive: the use of sediment profile imagery. Marine Pollution Bulletin, 58(4): 565–572.
  • Rosenberg, R., H. C. Nilsson, B. Hellman and S. Agrenius (2000). Depth Correlated Benthic Faunal Quantity and Infaunal Burrow Structures on the Slopes of a Marine Depression. Estuarine, Coastal and Shelf Science, 50(6): 843–853.
  • Røstad, A., S. Kaartvedt, T. A. Klevjer and W. Melle (2006). Fish are attracted to vessels. ICES Journal of Marine Science, 63(8): 1431–1437.
  • Rouse, S., N. C. Lacey, P. Hayes and T. A. Wilding (2019). Benthic Conservation Features and Species Associated With Subsea Pipelines: Considerations for Decommissioning. Frontiers in Marine Science, 6: 200.
  • Royal HaskoningDHV (2013). The Kyle Rhea Tidal Stream Array Environmental Statement: Volume 3—Appendices. Marine Scotland, Aberdeen, Scotland, UK: p. 829.
  • Royal HaskoningDHV (2014). Perpetuus Tidal Energy Centre Non-Technical Summary. PTEC Limited, Isle of Wight, UK: p. 34.
  • Šaškov, A., T. G. Dahlgren, Y. Rzhanov and M.-L. Schläppy (2015). Comparison of manual and semi-automatic underwater imagery analyses for monitoring of benthic hard-bottom organisms at offshore renewable energy installations. Hydrobiologia, 756: 139–153.
  • Schmitt, P., R. Culloch and L. Lieber (2016). Environmental Monitoring Baseline Report of the H2020 project PowerKite. Queen’s University Belfast, Northern Ireland, UK: p. 16.
  • Schramm, K. D., M. J. Marnane, T. S. Elsdon, C. Jones, B. J. Saunders, J. S. Goetze, D. Driessen, L. A. F. Fullwood and E. S. Harvey (2020). A comparison of stereo-BRUVs and stereo-ROV techniques for sampling shallow water fish communities on and off pipelines. Marine Environmental Research, 162: 105198.
  • Schultz, A. L., H. A. Malcolm, R. Ferrari and S. D. A. Smith (2019). Wave energy drives biotic patterns beyond the surf zone: Factors influencing abundance and occurrence of mobile fauna adjacent to subtropical beaches. Regional Studies in Marine Science, 25: 100467.
  • Schutter, M., M. Dorenbosch, F. M. F. Driessen, W. Lengkeek, O. G. Bos and J. W. P. Coolen (2019). Oil and gas platforms as artificial substrates for epibenthic North Sea fauna: Effects of location and depth. Journal of Sea Research, 153: 101782.
  • ScottishPower Renewables Ltd. (2010). Sound of Islay Demonstration Tidal Array Environmental Statement. Marine Scotland, Aberdeen, Scotland, UK: p. 445.
  • Sempere-Valverde, J., E. Ostalé-Valriberas, G. M. Farfán and F. Espinosa (2018). Substratum type affects recruitment and development of marine assemblages over artificial substrata: A case study in the Alboran Sea. Estuarine, Coastal and Shelf Science, 204: 56–65.
  • Sheehan, E. V., D. Bridger, S. J. Nancollas and S. J. Pittman (2020). PelagiCam: a novel underwater imaging system with computer vision for semi-automated monitoring of mobile marine fauna at offshore structures. Environmental Monitoring and Assessment, 192(1): 11.
  • Sheehan, K. (2009). Wave Energy Test Site Galway Bay. Marine Institute, Galway, Ireland: p. 13.
  • Shumchenia, E. J., M. L. Guarinello and J. W. King (2016). A Re-assessment of Narragansett Bay Benthic Habitat Quality Between 1988 and 2008. Estuaries and Coasts, 39: 1463–1477.
  • Simone, M. and J. Grant (2020). Visually-based alternatives to sediment environmental monitoring. Marine Pollution Bulletin, 158: 111367.
  • Smith, R. and M. A. Adonizio (2011). Roosevelt Island Tidal Energy (RITE) Environmental Assessment Project Final Report. New York State Energy Research and Development Authority, NYSERDA 9892-1, New York, NY, USA: p. 56.
  • Soldal, A. V., I. Svellingen, T. Jorgensen and S. Lokkeborg (2002). Rigs-to-reefs in the North Sea: hydroacoustic quantification of fish in the vicinity of a semi-cold platform. ICES Journal of Marine Science, 59: S281-S287.
  • Sparling, C. E., E. Cox and D. J. F. Russell (2013). DP Energy Seal Telemetry. SMRU Ltd. report SMRUL-DPE-2013-013: p. 14.
  • Spencer, M. L., A. W. Stoner, C. H. Ryer and J. E. Munk (2005). A towed camera sled for estimating abundance of juvenile flatfishes and habitat characteristics: Comparison with beam trawls and divers. Estuarine, Coastal and Shelf Science, 64(2–3): 497–503.
  • Stewart, P. L. (2009). Seabed Video and Photographic Survey—Berth A and Cable Route—Minas Passage Tidal Energy Study Site, July & August, 2009. Fundy Ocean Research Centre for Energy (FORCE), Hantsport, NS, Canada: p. 106.
  • Stewart, P. L. (2009). Seabed Video and Photographic Survey—Berth C and Cable Route—Minas Passage Tidal Energy Study Site, February, March, June, and July, 2009. Fundy Ocean Research Centre for Energy (FORCE), Hantsport, NS, Canada: p. 161.
  • Stewart, P. L. and H. A. Levy (2010). Seabed Video and Photographic Survey—Berth B and Cable Route—Minas Passage Tidal Energy Study Site, July & August, 2009. Fundy Ocean Research Centre for Energy (FORCE), Hantsport, NS, Canada: p. 115.
  • Streich, M. K., M. J. Ajemian, J. J. Wetz and G. W. Stunz (2017). A Comparison of Fish Community Structure at Mesophotic Artificial Reefs and Natural Banks in the Western Gulf of Mexico. Marine and Coastal Fisheries: Dynamics, Management, and Ecosystem Science, 9(1): 170–189.
  • Sustainable Energy Authority of Ireland (SEAI) (2011). Appendix 3 Ecological assessment for the proposed Atlantic Marine Energy Test Site. Atlantic Marine Energy Test Site Environmental Impact Statement, Sustainable Energy Authority of Ireland, Dublin, Ireland: p 324.
  • Sustainable Energy Authority of Ireland (SEAI) (2011). Chapter 6 Flora and Fauna. Atlantic Marine Energy Test Site Environmental Impact Statement, Sustainable Energy Authority of Ireland, Dublin, Ireland: p. 40.
  • Sustainable Energy Authority of Ireland (SEAI) (2011). Chapter 8—Soils, geology and groundwater. Atlantic Marine Energy Test Site Environmental Impact Statement, Sustainable Energy Authority of Ireland, Dublin, Ireland: p 16.
  • Sutula, M., L. Green, G. Cicchetti, N. Detenbeck and P. Fong (2014). Thresholds of Adverse Effects of Macroalgal Abundance and Sediment Organic Matter on Benthic Habitat Quality in Estuarine Intertidal Flats. Estuaries and Coasts, 37: 1532–1548.
  • Taormina, B., M. Laurans, M. P. Marzloff, N. Dufournaud, M. Lejart, N. Desroy, D. Leroy, S. Martin and A. Carlier (2020). Renewable energy homes for marine life: Habitat potential of a tidal energy project for benthic megafauna. Marine Environmental Research, 161: 105131.
  • Taormina, B., M. P. Marzloff, N. Desroy, X. Caisey, O. Dugornay, E. Metral Thiesse, A. Tancray and A. Carlier (2020). Optimizing image-based protocol to monitor macroepibenthic communities colonizing artificial structures. ICES Journal of Marine Science, 77(2): 835–845.
  • Taormina, B., A. Percheron, M. P. Marzloff, X. Caisey, N. Quillien, M. Lejart, N. Desroy, O. Dugornay, A. Tancray and A. Carlier (2020). Succession in epibenthic communities on artificial reefs associated with marine renewable energy facilities within a tide-swept environment. ICES Journal of Marine Science, 77(7–8): 2656–2668.
  • Tassetti, A. N., A. Minelli, C. Ferra, S. Guicciardi, A. Gaetani and G. Fabi (2020). An integrated approach to assess fish spatial pattern around offshore gas platforms: A pilot study in the Adriatic Sea. Marine Environmental Research, 162: 105100.
  • Taylor, J. C., A. B. Paxton, C. M. Voss, B. Sumners, C. A. Buckel, J. Vander Pluym, E. B. Ebert, T. S. Viehman, S. R. Fegley, E. A. Pickering, A. M. Adler, C. Freeman and C. H. Peterson (2016). Benthic Habitat Mapping and Assessment in the Wilmington-East Wind Energy Call Area: Final Report. U.S. Department of the Interior, Bureau of Ocean Energy Management (BOEM), OCS Study BOEM 2016-003 and NOAA Technical Memorandum 196: p. 171.
  • Terrill, S., S. Kramer, P. Nelson and D. Zajanc (2009). Baseline Data and Power Analyses for the OWET Dungeness Crab and Fish Baseline Study. Oregon Wave Energy Trust, Portland, OR, USA: p. 40.
  • Thuringer, P. and R. Reidy (2006). Summary Report on Environmental Monitoring Related to the Pearson College—ENCANA—Clean Current Tidal Power Demonstration Project at Race Rocks Ecological Reserve: Final Report. Archipelago Marine Research Ltd., Victoria, BC, Canada: p. 54.
  • Tiano, J. C., K. J. van der Reijden, S. O’Flynn, O. Beauchard, S. van der Ree, J. van der Wees, T. Ysebaert and K. Soetaert (2020). Experimental bottom trawling finds resilience in large-bodied infauna but vulnerability for epifauna and juveniles in the Frisian Front. Marine Environmental Research, 159: 104964.
  • Tidal Lagoon Swansea Bay plc (2014). Swansea Bay Tidal Lagoon Adaptive Environmental Management Plan—Revision 4. Tidal Lagoon Power, Swansea, Wales, UK: p. 212.
  • Todd, V. L. G., E. W. Lavallin and P. I. Macreadie (2018). Quantitative analysis of fish and invertebrate assemblage dynamics in association with a North Sea oil and gas installation complex. Marine Environmental Research, 142: 69–79.
  • Todd, V. L. G., L. D. Williamson, S. E. Cox, I. B. Todd and P. I. Macreadie (2020). Characterizing the first wave of fish and invertebrate colonization on a new offshore petroleum platform. ICES Journal of Marine Science, 77(3): 1127–1136.
  • Tolimieri, N., M. E. Clarke, J. Clemons, W. Wakefield and A. Powell (2020). The abundance and habitat use of demersal fishes on a rocky offshore bank using the ROPOS remotely operated vehicle. Deep Sea Research Part I: Oceanographic Research Papers, 157: 103193.
  • Uhlenkott, K., A. Vink, T. Kuhn and P. Martínez Arbizu (2020). Predicting meiofauna abundance to define preservation and impact zones in a deep-sea mining context using random forest modelling. Journal of Applied Ecology, 57(7): 1210–1221.
  • Umehara, A., S. Nakai, T. Okuda, M. Ohno and W. Nishijima (2019). Benthic quality assessment using M-AMBI in the Seto Inland Sea, Japan. Marine Environmental Research, 148: 67–74.
  • U.S. Department of Energy (DOE) (2012). Oregon State University and Northwest National Marine Renewable Energy Center Wave Energy Test Project—Final Environmental Assessment. US Department of Energy (DOE), DOE/EA-1917, Golden, CO, USA: p. 166.
  • van Deurs, M., T. M. Grome, M. Kaspersen, H. Jensen, C. Stenberg, T. K. Sørensen, J. Støttrup, T. Warnar and H. Mosegaard (2012). Short- and long-term effects of an offshore wind farm on three species of sandeel and their sand habitat. Marine Ecology Progress Series, 458: 169–180.
  • van Hal, R., A. B. Griffioen and O. A. van Keeken (2017). Changes in fish communities on a small spatial scale, an effect of increased habitat complexity by an offshore wind farm. Marine Environmental Research, 126: 26–36.
  • Van Hoey, G., S. N. R. Birchenough and K. Hostens (2014). Estimating the biological value of soft-bottom sediments with sediment profile imaging and grab sampling. Journal of Sea Research 86: 1–12.
  • Verdant Power (2019). Roosevelt Island Tidal Energy Project FERC No. P-12611 Article 401 RMEE Plan Amendments. Verdant Power LLC, New York, NY, USA: p. 168.
  • Waggitt, J. J., P. W. Cazenave, R. Torres, B. J. Williamson and B. E. Scott (2016). Quantifying pursuit-diving seabirds’ associations with fine-scale physical features in tidal stream environments. Journal of Applied Ecology, 53: 1653–1666.
  • Want, A., R. Crawford, J. Kakkonen, G. Kiddie, S. Miller, R. E. Harris and J. S. Porter (2017). Biodiversity characterisation and hydrodynamic consequences of marine fouling communities on marine renewable energy infrastructure in the Orkney Islands Archipelago, Scotland, UK. Biofouling, 33(7): 567–579.
  • Wetz, J. J., M. J. Ajemian, B. Shipley and G. W. Stunz (2020). An assessment of two visual survey methods for documenting fish community structure on artificial platform reefs in the Gulf of Mexico. Fisheries Research, 225: 105492.
  • Wilhelmsson, D., T. Malm and M. C. Öhman (2006). The influence of offshore windpower on demersal fish. ICES Journal of Marine Science, 63: 775–784.
  • Williamson, B., S. Fraser, L. Williamson, V. Nikora and B. Scott (2019). Predictable changes in fish school characteristics due to a tidal turbine support structure. Renewable Energy, 141: 1092–1102.
  • Williamson, B. J., S. Fraser, P. Blondel, P. S. Bell, J. J. Waggitt and B. E. Scott (2017). Multisensor Acoustic Tracking of Fish and Seabird Behavior Around Tidal Turbine Structures in Scotland. IEEE Journal of Oceanic Engineering, 42(4): 948–965.
  • Wilson, S. J., T. J. Fredette, J. D. Germano, J. A. Blake, P. L. Neubert and D. A. Carey (2009). Plan-view photos, benthic grabs, and sediment-profile images: Using complementary techniques to assess response to seafloor disturbance. Marine Pollution Bulletin, 59(1–3): 26–37.
  • Zhulay, I., K. Iken, P. E. Renaud and B. A. Bluhm (2019). Epifaunal communities across marine landscapes of the deep Chukchi Borderland (Pacific Arctic). Deep Sea Research Part I: Oceanographic Research Papers, 151: 103065.

References

  1. European Parliament and European Council. Water Framework Directive 2000/06/EC; OJL 3277, 22.12.2000; European Parliament and European Council: Brussels, Belgium, 2000; p. 73. [Google Scholar]
  2. European Parliament and European Council. Habitat Directive 92/43/EEC; OJL 206, 22.7.1992; European Parliament and European Council: Brussels, Belgium, 1992; p. 50. [Google Scholar]
  3. European Parliament and European Council. Marine Strategy Framework Directive 2008/56/EC; OJL 164, 25.6.2008; European Parliament and European Council: Brussels, Belgium, 2008; p. 40. [Google Scholar]
  4. Clean Water Act of 1972. 33 U.S.C. § 1251 et seq, 1972.
  5. Endangered Species Act of 1973. 16 U.S.C. ch. 35 § 1531 et seq, 1973.
  6. Fish and Wildlife Coordination Act of 1980. 16 USC § 2901 et seq, 1980.
  7. Magnuson-Stevens Fishery Conservation and Management Act of 2007. 16 USC § 1801 et seq, 2007.
  8. Bender, A.; Francisco, F.G.; Sundberg, J. A review of methods and models for environmental monitoring of marine renewable energy. In Proceedings of the European Wave and Tidal Energy Conference (EWTEC), Cork, Ireland, 27 August–1 September 2017. [Google Scholar]
  9. Hemery, L.G. 2020 State of the Science Report, Chapter 6: Changes in Benthic and Pelagic Habitats Caused by Marine Renewable Energy Devices; Copping, A.E., Hemery, L.G., Eds.; Ocean Energy Systems (OES): Richland, WA, USA, 2020; pp. 104–125. [Google Scholar]
  10. Gray, J.S.; Elliott, M. Ecology of Marine Sediments: From Science to Management, 2nd ed.; Oxford University Press: Oxford, UK, 2009. [Google Scholar]
  11. Holte, B.; Buhl-Mortensen, L. Does grab size influence sampled macrofauna composition? A test conducted on deep-sea communities in the northeast Atlantic. Mar. Environ. Res. 2020, 154, 104867. [Google Scholar] [CrossRef] [PubMed]
  12. Callaway, R. Historical Data Reveal 30-Year Persistence of Benthic Fauna Associations in Heavily Modified Waterbody. Front. Mar. Sci. 2016, 3, 141. [Google Scholar] [CrossRef] [Green Version]
  13. Grimm, V.; Wissel, C. Babel, or the ecological stability discussions: An inventory and analysis of terminology and a guide for avoiding confusion. Oecologia 1997, 109, 323–334. [Google Scholar] [CrossRef] [PubMed]
  14. Kingsford, M.; Battershill, C. Studying Temperate Environments; Canterbury University Press: Christchurch, New Zealand, 1998; p. 335. [Google Scholar]
  15. Hubert, W.A.; Pope, K.L.; Dettmers, J.M. Passive Capture Techniques, 3rd ed.; Zale, A.V., Parrish, D.L., Sutton, T.M., Eds.; American Fisheries Society: Bethesda, MD, USA, 2012. [Google Scholar]
  16. Thistle, D. The Deep-Sea Floor: An Overview. In Ecosystems of the Deep Oceans; Tyler, P.A., Ed.; Elsevier Science B.V.: Amsterdam, The Netherlands, 2002; pp. 5–37. [Google Scholar]
  17. Birchenough, S.N.R.; Boyd, S.E.; Coggan, R.A.; Limpenny, D.S.; Meadows, W.J.; Rees, H.L. Lights, camera and acoustics: Assessing macrobenthic communities at a dredged material disposal site off the North East coast of the UK. J. Mar. Syst. 2006, 62, 204–216. [Google Scholar] [CrossRef]
  18. International Organization for Standardization (ISO). Water Quality–Guidelines for Quantitative Sampling and Sample Processing of Marine Soft-Bottom Macrofauna; ISO: Geneva, Switzerland, 2014; p. 40. [Google Scholar]
  19. International Organization for Standardization (ISO). Water Quality–Guidance on Marine Biological Surveys of Hard-Substrate Communities; ISO: Geneva, Switzerland, 2007; p. 28. [Google Scholar]
  20. Environmental Protection Agency (EPA). Evaluation of Dredged Material Proposed for Discharge in Waters of the U.S.–Testing Manual; U.S. EPA: Washington, DC, USA, 1998; p. 176.
  21. Environmental Protection Agency (EPA). Guidance on Choosing a Sampling Design for Environmental Data Collection for Use in Developing a Quality Assurance Project Plan; U.S. EPA: Washington, DC, USA, 2002; p. 178.
  22. Minerals Management Service (MMS). Notice to Lessees and Operators (NTL) of Federal Oil and Gas Leases in the Pacific Outer Continental Shelf Region–Biological Survey and Report Requirements; U.S. MMS: Sterling, VI, USA, 2006; p. 8.
  23. Minerals Management Service (MMS). Notice to Lessees and Operators of Federal Oil, Gas and Sulphur Leases and Pipeline Right-of-Way Holders in the Outer Continental Shelf, Gulf of Mexico OCS Region–Shallow Hazards Program; U.S. MMS: New Orleans, LA, USA, 2008; p. 18.
  24. Minerals Management Service (MMS). Notice to Lessees and Operators of Federal Oil, Gas and Sulphur Leases and Pipeline Right-of-Way Holders in the Outer Continental Shelf, Gulf of Mexico OCS Region–Biologically-Sensitive Underwater Features and Areas; U.S. MMS: New Orleans, LA, USA, 2009; p. 22.
  25. Minerals Management Service (MMS). Notice to Lessees and Operators of Federal Oil, Gas and Sulphur Leases and Pipeline Right-of-Way Holders in the Outer Continental Shelf, Gulf of Mexico OCS Region–Deepwater Benthic Communities; U.S. MMS: New Orleans, LA, USA, 2009; p. 9.
  26. Bureau of Ocean Energy Management (BOEM). Guidelines for Providing Benthic Habitat Survey Information for Renewable Energy Development on the Atlantic Outer Continental Shelf Pursuant to 30 CFR Part 585; U.S. BOEM: Sterling, VI, USA, 2019; p. 9.
  27. Bureau of Ocean Energy Management (BOEM). Guidelines for Providing Information on Fisheries for Renewable Energy Development on the Atlantic Outer Continental Shelf Pursuant to 30 CFR Part 585; U.S. BOEM: Sterling, VI, USA, 2019; p. 14.
  28. Bureau of Ocean Energy Management (BOEM). Guidelines for Providing Geophysical, Geotechnical, and Geohazard Information Pursuant to 30 CFR Part 585; U.S. BOEM: Sterling, VI, USA, 2020; p. 32.
  29. Centre for Environment Fisheries and Aquaculture Science (CEFAS). Guidelines for the Conduct of Benthic Studies at Aggregate Dredging Sites; Burnham Laboratory: Burnham-on-Crouch, UK, 2002; p. 199. [Google Scholar]
  30. Centre for Environment Fisheries and Aquaculture Science (CEFAS). Guidelines for Data Acquisition to Support Marine Environmental Assessments for Offshore Renewable Energy Projects; CEFAS contract report ME5403-Modul 15; CEFAS, Lowestoft: Suffolk, UK, 2011; p. 97. [Google Scholar]
  31. Davies, J.; Baxter, J.; Bradley, M.; Connor, D.; Khan, J.; Murray, E.; Sanderson, W.; Turnbull, C.; Vincent, M. Marine Monitoring Handbook; Joint Nature Conservation Committee: Peterborough, UK, 2001. [Google Scholar]
  32. Garel, E.; Rey, C.C.; Ferreira, Ó.; van Koningsveld, M. Applicability of the “Frame of Reference” approach for environmental monitoring of offshore renewable energy projects. J. Environ. Manag. 2014, 141, 16–28. [Google Scholar] [CrossRef] [Green Version]
  33. Gonzalez, S.; Horne, J.K.; Ward, E. Temporal variability in pelagic biomass distributions at wave and tidal sites and implications for standardization of biological monitoring. Int. Mar. Energy J. 2019, 2, 15–28. [Google Scholar] [CrossRef]
  34. Copping, A.E.; Gorton, A.M.; Freeman, M.C.; Rose, D.; Farr, H. Data Transferability and Collection Consistency in Marine Renewable Energy: An Update to the 2018 Report; PNNL-27995 Rev. 1; Pacific Northwest National Lab.(PNNL): Richland, WA, USA, 2020; p. 49.
  35. Dempster, T.; Sanchez-Jerez, P.; Bayle-Sempere, J.T.; Gimenez-Casalduero, F.; Valle, C. Attraction of wild fish to sea-cage fish farms in the south-western Mediterranean Sea: Spatial and short-term temporal variability. Mar. Ecol. Prog. Ser. 2002, 242, 237–252. [Google Scholar] [CrossRef]
  36. Greene, H.G. Habitat characterization of a tidal energy site using an ROV: Overcoming difficulties in a harsh environment. Cont. Shelf Res. 2015, 106, 85–96. [Google Scholar] [CrossRef]
  37. Mack, L.; Attila, J.; Aylagas, E.; Beermann, A.; Borja, A.; Hering, D.; Kahlert, M.; Leese, F.; Lenz, R.; Lehtiniemi, M.; et al. A synthesis of marine monitoring methods with the potential to enhance the status assessment of the Baltic Sea. Front. Mar. Sci. 2020, 7, 823. [Google Scholar] [CrossRef]
  38. Thomas, R. Marine Biology: An Ecological Approach; ED-Tech Press: Waltham Abbey Essex, UK, 2019. [Google Scholar]
  39. Whiting, J.M.; Copping, A.E.; Freeman, M.C.; Woodbury, A.E. Tethys knowledge management system: Working to advance the marine renewable energy industry. Int. Mar. Energy J. 2019, 2, 29–38. [Google Scholar] [CrossRef]
  40. Copping, A.E.; Sather, N.; Hanna, L.; Whiting, J.; Zydlewski, G.; Staines, G.; Gill, A.; Hutchison, I.; O’Hagan, A.M.; Simas, T.; et al. Annex IV 2016 State of the Science Report: Environmental Effects of Marine Renewable Energy Development around the World; Ocean Energy Systems (OES): Richland, WA, USA, 2016; p. 224. [Google Scholar]
  41. Copping, A.E.; Hemery, L.G. OES-Environmental 2020 State of the Science Report: Environmental Effects of Marine Renewable Energy Development around the World; Ocean Energy Systems (OES): Richland, WA, USA, 2020; p. 327. [Google Scholar]
  42. Love, M.S.; Nishimoto, M.M.; Snook, L.; Kui, L. An analysis of the sessile, structure-forming invertebrates living on California oil and gas platforms. Bull. Mar. Sci. 2019, 95, 583–596. [Google Scholar] [CrossRef]
  43. Schutter, M.; Dorenbosch, M.; Driessen, F.M.F.; Lengkeek, W.; Bos, O.G.; Coolen, J.W.P. Oil and gas platforms as artificial substrates for epibenthic North Sea fauna: Effects of location and depth. J. Sea Res. 2019, 153, 101782. [Google Scholar] [CrossRef]
  44. Todd, V.L.G.; Lavallin, E.W.; Macreadie, P.I. Quantitative analysis of fish and invertebrate assemblage dynamics in association with a North Sea oil and gas installation complex. Mar. Environ. Res. 2018, 142, 69–79. [Google Scholar] [CrossRef]
  45. McIlvenny, J.; Tamsett, D.; Gillibrand, P.; Goddijn-Murphy, L. On the Sediment Dynamics in a Tidally Energetic Channel: The Inner Sound, Northern Scotland. J. Mar. Sci. Eng. 2016, 4, 31. [Google Scholar] [CrossRef] [Green Version]
  46. Rosenberg, R.; Magnusson, M.; Nilsson, H.C. Temporal and spatial changes in marine benthic habitats in relation to the EU Water Framework Directive: The use of sediment profile imagery. Mar. Pollut. Bull. 2009, 58, 565–572. [Google Scholar] [CrossRef] [PubMed]
  47. Tiano, J.C.; van der Reijden, K.J.; O’Flynn, S.; Beauchard, O.; van der Ree, S.; van der Wees, J.; Ysebaert, T.; Soetaert, K. Experimental bottom trawling finds resilience in large-bodied infauna but vulnerability for epifauna and juveniles in the Frisian Front. Mar. Environ. Res. 2020, 159, 104964. [Google Scholar] [CrossRef] [PubMed]
  48. Meyer-Gutbrod, E.L.; Love, M.S.; Claisse, J.T.; Page, H.M.; Schroeder, D.M.; Miller, R.J. Decommissioning impacts on biotic assemblages associated with shell mounds beneath southern California offshore oil and gas platforms. Bull. Mar. Sci. 2019, 95, 683–701. [Google Scholar] [CrossRef]
  49. Ajemian, M.J.; Wetz, J.J.; Shipley-Lozano, B.; Stunz, G.W. Rapid assessment of fish communities on submerged oil and gas platform reefs using remotely operated vehicles. Fish. Res. 2015, 167, 143–155. [Google Scholar] [CrossRef]
  50. Gates, A.R.; Horton, T.; Serpell-Stevens, A.; Chandler, C.; Grange, L.J.; Robert, K.; Bevan, A.; Jones, D.O.B. Ecological Role of an Offshore Industry Artificial Structure. Front. Mar. Sci. 2019, 6, 675. [Google Scholar] [CrossRef] [Green Version]
  51. Broadhurst, M.; Orme, C.D. Spatial and temporal benthic species assemblage responses with a deployed marine tidal energy device: A small scaled study. Mar. Environ. Res. 2014, 99, 76–84. [Google Scholar] [CrossRef] [PubMed]
  52. Hemery, L.G.; Henkel, S.K.; Cochrane, G.R. Benthic assemblages of mega epifauna on the Oregon continental margin. Cont. Shelf Res. 2018, 159, 24–32. [Google Scholar] [CrossRef]
  53. Krone, R.; Gutow, L.; Joschko, T.J.; Schroder, A. Epifauna dynamics at an offshore foundation–Implications of future wind power farming in the North Sea. Mar. Environ. Res. 2013, 85, 1–12. [Google Scholar] [CrossRef] [PubMed]
  54. Cochrane, G.R.; Hemery, L.G.; Henkel, S.K. Oregon OCS Seafloor Mapping: Selected Lease Blocks Relevant to Renewable Energy; U.S. Geological Survey Open-File Report 2017-1045 and Bureau of Ocean Energy Management OCS Study BOEM 2017-018; USGS: Reston, VI, USA, 2017; p. 57.
  55. HDR. Benthic Monitoring during Wind Turbine Installation and Operation at the Block Island Wind Farm, Rhode Island; OCS Study BOEM 2018-047; U.S. BOEM: Sterling, VI, USA, 2018; p. 155.
  56. Connor, D.W.; Allen, J.H.; Golding, N.; Howell, K.L.; Lieberknecht, L.M.; Northen, K.O.; Reker, J.B. The Marine Habitat Classification for Britain and Ireland; Version 04.05; Joint Nature Conservation Committee: Peterborough, UK, 2004; p. 49.
  57. Centre for Marine and Coastal Studies Ltd. (CMACS). Deep Green Project Holyhead Deep Benthic Technical Report; CMACS Ltd.: Eastham, UK, 2015; p. 106. [Google Scholar]
  58. Kregting, L.; Elsaesser, B.; Kennedy, R.; Smyth, D.; O’Carroll, J.; Savidge, G. Do Changes in Current Flow as a Result of Arrays of Tidal Turbines Have an Effect on Benthic Communities? PLoS ONE 2016, 11, e0161279. [Google Scholar] [CrossRef] [Green Version]
  59. Horne, J.; Jacques, D.; Parker-Stetter, S.; Linder, H.; Nomura, J. Evaluating Acoustic Technologies to Monitor Aquatic Organisms at Renewable Energy Sites: Final Report; BOEM 2014-057; U.S. BOEM: Sterling, VI, USA, 2013; p. 102.
  60. Ocean Renewable Power Company (ORPC) Maine. Cobscook Bay Tidal Energy Project: 2013 Environmental Monitoring Report; FERC PROJECT NO. P-12711-005; ORPC: Portland, ME, USA, 2014; p. 502. [Google Scholar]
  61. Foubister, L. EMEC Tidal Test Facility Fall of Warness Eday, Orkney: Environmental Statement; EMEC: Stromness, UK, 2005; p. 176. [Google Scholar]
  62. Bender, A.; Sundberg, J. Effects of Wave Energy Generators on Nephrops norvegicus. In Proceedings of the Asian Wave and Tidal Energy Conference (AWTEC), Taipei, Taiwan, 9–13 September 2018. [Google Scholar]
  63. Fields, S.; Henkel, S.; Roegner, G.C. Video sleds effectively survey epibenthic communities at dredged material disposal sites. Environ. Monit. Assess. 2019, 191, 404. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  64. Pearce, B.; Fariñas-Franco, J.M.; Wilson, C.; Pitts, J.; deBurgh, A.; Somerfield, P.J. Repeated mapping of reefs constructed by Sabellaria spinulosa Leuckart 1849 at an offshore wind farm site. Cont. Shelf Res. 2014, 83, 3–13. [Google Scholar] [CrossRef]
  65. Van Hoey, G.; Birchenough, S.N.R.; Hostens, K. Estimating the biological value of soft-bottom sediments with sediment profile imaging and grab sampling. J. Sea Res. 2014, 86, 1–12. [Google Scholar] [CrossRef]
  66. O’Carroll, J.P.J.; Kennedy, R.M.; Creech, A.; Savidge, G. Tidal Energy: The benthic effects of an operational tidal stream turbine. Mar. Environ. Res. 2017, 129, 277–290. [Google Scholar] [CrossRef]
  67. Pattison, L.; Serrick, A.; Brown, C. Testing 360 Degree Imaging Technologies for Improved Animal Detection around Tidal Energy Installations; OERA: Halifax, NS, Canada, 2020; p. 97. [Google Scholar]
  68. Page, H.M.; Dugan, J.E.; Dugan, D.S.; Richards, J.B.; Hubbard, D.M. Effects of an offshore oil platform on the distribution and abundance of commercially important crab species. Mar. Ecol. Prog. Ser. 1999, 185, 47–57. [Google Scholar] [CrossRef]
  69. Thuringer, P.; Reidy, R. Summary Report on Environmental Monitoring Related to the Pearson College-ENCANA-Clean Current Tidal Power Demonstration Project at Race Rocks Ecological Reserve: Final Report; Archipelago Marine Research Ltd.: Victoria, BC, Canada, 2006; p. 54. [Google Scholar]
  70. Spanier, E.; Cobb, J.S.; Clancy, M. Impacts of remotely operated vehicles (ROVs) on the behavior of marine animals: An example using American lobsters. Mar. Ecol. Prog. Ser. 1994, 104, 257–266. [Google Scholar] [CrossRef]
  71. Stoner, A.W.; Ryer, C.H.; Parker, S.J.; Auster, P.J.; Wakefield, W.W. Evaluating the role of fish behavior in surveys conducted with underwater vehicles. Can. J. Fish. Aquat. Sci. 2008, 65, 1230–1243. [Google Scholar] [CrossRef]
  72. Cruz-Marrero, W.; Cullen, D.W.; Gay, N.R.; Stevens, B.G. Characterizing the benthic community in Maryland’s offshore wind energy areas using a towed camera sled: Developing a method to reduce the effort of image analysis and community description. PLoS ONE 2019, 14, e0215966. [Google Scholar] [CrossRef] [PubMed]
  73. Sheehan, E.V.; Bridger, D.; Nancollas, S.J.; Pittman, S.J. PelagiCam: A novel underwater imaging system with computer vision for semi-automated monitoring of mobile marine fauna at offshore structures. Environ. Monit. Assess. 2020, 192, 11. [Google Scholar] [CrossRef]
  74. Taylor, J.C.; Paxton, A.B.; Voss, C.M.; Sumners, B.; Buckel, C.A.; Vander Pluym, J.; Ebert, E.B.; Viehman, T.S.; Fegley, S.R.; Pickering, E.A.; et al. Benthic Habitat Mapping and Assessment in the Wilmington-East Wind Energy Call Area: Final Report; OCS Study BOEM 2016-003 and NOAA Technical Memorandum 196; U.S. BOEM: Sterling, VI, USA, 2016; p. 171.
  75. DP Energy Marine. West Islay Tidal Energy Park Environmental Statement; DP Marine Energy Ltd.: Buttevant, Ireland, 2013; p. 139. [Google Scholar]
  76. Foster-Smith & Foster-Smith. Kyle Rhea Benthic Video Survey; SeaGeneration (Kyle Rhea) Ltd.: Exeter, UK, 2012; p. 35. [Google Scholar]
  77. Soldal, A.V.; Svellingen, I.; Jorgensen, T.; Lokkeborg, S. Rigs-to-reefs in the North Sea: Hydroacoustic quantification of fish in the vicinity of a “semi-cold” platform. ICES J. Mar. Sci. 2002, 59, S281–S287. [Google Scholar] [CrossRef] [Green Version]
  78. Spencer, M.L.; Stoner, A.W.; Ryer, C.H.; Munk, J.E. A towed camera sled for estimating abundance of juvenile flatfishes and habitat characteristics: Comparison with beam trawls and divers. Estuar. Coast. Shelf Sci. 2005, 64, 497–503. [Google Scholar] [CrossRef]
  79. Oregon State University (OSU); Northwest National Marine Renewable Energy Center (NNMREC). Wave Energy Test Project-Final Environmental Assessment. Appendix E, Monitoring Plans; OSU: Corvallis, OR, USA, 2012; p. 18. [Google Scholar]
  80. Verdant Power. Benthic Habitat Characterization; FERC No. 12611; U.S. FERC: Washington, DC, USA, 2006; p. 97.
  81. Integral Consulting. Environmental Monitoring Program Report 2: Results of Phases I-IV; Shell Exploration & Production Company: Anchorage, AK, USA, 2017; p. 410. [Google Scholar]
  82. Revelas, E.C.; Jones, C.; Sackmann, B.; Maher, N. A Benthic Habitat Monitoring Approach for Marine and Hydrokinetic Sites; Final Technical Report United States 10.2172/1638512 GFO; Integral Consulting, Inc.: Seattle, WA, USA, 2020. [Google Scholar]
  83. Smokorowski, K.E.; Randall, R.G. Cautions on using the Before-After-Control-Impact design in environmental effects monitoring programs. FACETS 2017, 2, 212–232. [Google Scholar] [CrossRef] [Green Version]
  84. Methratta, E.T.; Dardick, W.R. Meta-analysis of finfish abundance at offshore wind farms. Rev. Fish. Sci. Aquac. 2019, 27, 242–260. [Google Scholar] [CrossRef]
  85. Punzo, E.; Strafella, P.; Scarcella, G.; Spagnolo, A.; De Biasi, A.M.; Fabi, G. Trophic structure of polychaetes around an offshore gas platform. Mar. Pollut. Bull. 2015, 99, 119–125. [Google Scholar] [CrossRef]
  86. Bailey, H.; Brookes, K.L.; Thompson, P.M. Assessing environmental impacts of offshore wind farms: Lessons learned and recommendations for the future. Aquat. Biosyst. 2014, 10, 8. [Google Scholar] [CrossRef] [Green Version]
  87. Ellis, J.I.; Schneider, D.C. Evaluation of a gradient sampling design for environmental impact assessment. Environ. Monit. Assess. 1997, 48, 157–172. [Google Scholar] [CrossRef]
  88. Aquatera Ltd. SSF Scapa Flow Sites Benthic ROV Survey St Margaret’s Hope; P584 Version 1; Aquatera Ltd.: Stromness, UK, 2015; p. 26. [Google Scholar]
  89. Argyll Tidal Limited. Environmental Appraisal (EA) for the Argyll Tidal Demonstrator Project; RES Ltd., East Kilbride: Lanarkshire, UK, 2013; p. 207. [Google Scholar]
  90. Sustainable Energy Authority of Ireland (SEAI). Chapter 6 Flora and Fauna. In Atlantic Marine Energy Test Site Environmental Impact Statement; Sustainable Energy Authority of Ireland: Dublin, Ireland, 2011; p. 40. [Google Scholar]
  91. Umehara, A.; Nakai, S.; Okuda, T.; Ohno, M.; Nishijima, W. Benthic quality assessment using M-AMBI in the Seto Inland Sea, Japan. Mar. Environ. Res. 2019, 148, 67–74. [Google Scholar] [CrossRef]
  92. Degraer, S.; Brabant, R.; Rumes, B.; Vigin, L. (Eds.) Environmental Impacts of Offshore Wind Farms in the Belgian Part of the North Sea: Marking a Decade of Monitoring, Research and Innovation; Royal Belgian Institute of Natural Sciences: Brussels, Belgium, 2019; p. 134. [Google Scholar]
Figure 1. Proportions of the different technologies used for describing habitats and measuring changes in their characteristics.
Figure 1. Proportions of the different technologies used for describing habitats and measuring changes in their characteristics.
Jmse 10 00092 g001
Figure 2. Heatmap showcasing the preponderance of sampling technologies across habitat categories; the darker the color, the more frequently used the technology. Only technologies that were used for two or more habitat categories are represented here.
Figure 2. Heatmap showcasing the preponderance of sampling technologies across habitat categories; the darker the color, the more frequently used the technology. Only technologies that were used for two or more habitat categories are represented here.
Jmse 10 00092 g002
Figure 3. Proportions of each four general reasons for choosing a technology per habitat category: custom-made technology, historical and/or geographical preference for a type of technology, opportunistic use of a technology, or ubiquitous aspect of a technology.
Figure 3. Proportions of each four general reasons for choosing a technology per habitat category: custom-made technology, historical and/or geographical preference for a type of technology, opportunistic use of a technology, or ubiquitous aspect of a technology.
Jmse 10 00092 g003
Figure 4. Heatmap showcasing the preponderance of sampling designs across habitat categories; the darker the color, the more frequently used the sampling design. When sampling designs are combined, the primary design is listed first and the secondary second. BACI/CR = before after control impact/control response.
Figure 4. Heatmap showcasing the preponderance of sampling designs across habitat categories; the darker the color, the more frequently used the sampling design. When sampling designs are combined, the primary design is listed first and the secondary second. BACI/CR = before after control impact/control response.
Jmse 10 00092 g004
Figure 5. Success, within the reviewed studies, in detecting changes or differences in habitats, within the survey area or before/after an event susceptible to trigger changes.
Figure 5. Success, within the reviewed studies, in detecting changes or differences in habitats, within the survey area or before/after an event susceptible to trigger changes.
Jmse 10 00092 g005
Figure 6. Proportion of positive, negative, or neutral feedback from the authors of the reviewed studies on the technologies used for surveying and monitoring the six categories of habitats. In many instances, the feedback could be classified as a combination of two or three options, when it was positive for some aspects of the work, negative for others, and neutral for yet others.
Figure 6. Proportion of positive, negative, or neutral feedback from the authors of the reviewed studies on the technologies used for surveying and monitoring the six categories of habitats. In many instances, the feedback could be classified as a combination of two or three options, when it was positive for some aspects of the work, negative for others, and neutral for yet others.
Jmse 10 00092 g006
Table 1. Information extracted from the documents surveyed in this literature review.
Table 1. Information extracted from the documents surveyed in this literature review.
Field of InformationDescription
TechnologySpecific technology/gear used.
Source reviewed Citation (reference) of document reviewed.
Document nameName given to the document internally.
Study goalBrief description of the general aim of the study in the document reviewed.
Site characteristicsBrief description of the site: depth, relative distance to shore, bottom type if known, current speed, etc.
Reason for selecting technologyBrief description, if provided, of why authors selected the technology.
Brand and modelIf specified, the brand and model of technology used.
CharacteristicsIf provided, a list of specific characteristics such as size, penetration depth, frequency, resolution, etc.
MethodsBrief description of the steps used to implement the technology.
Sampling designNumbers of stations, transects, replicates, and the like.
Data processingBrief description of how samples were handled from collection to analysis of results.
Successful identification of changeBrief description of the differences observed and the timeline, if any spatial and/or temporal changes and/or differences in habitat were observed.
Feedback after useIf provided, pros and cons of using the technology for achieving the study’s goal.
Usability for modelingNote about whether the data obtained can be used for modeling (as dependent or independent variables).
NotesAny additional notes upon reviewing documents.
Table 2. Group options for each field for which the information was synthesized across entries.
Table 2. Group options for each field for which the information was synthesized across entries.
Field of InformationGroup Options
Reason for selecting technologyCustom-made; historically or geographically preferred; opportunistic; ubiquitous.
Sampling designBefore after control impact or control/response; gradient; stratified; transects; stations; other; no information.
Successful identification of changeBaseline characterization; change/differences detected; no change/differences detected; no information.
Feedback after usePositive; neutral; negative; no information.
Table 3. Complete list of the sampling/surveying technologies compiled from the literature review and organized in technology classes. Technology acronyms are provided within brackets while secondary technologies are within parentheses.
Table 3. Complete list of the sampling/surveying technologies compiled from the literature review and organized in technology classes. Technology acronyms are provided within brackets while secondary technologies are within parentheses.
AcousticNet and Trawl
Acoustic backscatterBeam trawl
Acoustic cameraBenthic trawl
Acoustic Doppler current profiler [ADCP]Bongo net
Acoustic Doppler velocimeter [ADV]Box trawl
Acoustic ground-discrimination systems [AGDS]Campelen trawl
Autonomous underwater vehicle [AUV] (+bathymetric sonar)Drifting gillnet
Boomer seismic profilesElectric pulse trawl
Compressed high intensity radar pulse [CHIRP]Fyke net
Dual-frequency echosounderGill net
Fisheries echosounderHyperbenthic sledge
High-definition sonar (dual-frequency identification sonar)Midwater trawler
Multibeam echosounderOtter trawl
Multibeam sonarPelagic trawl
Passive acoustic telemetryPlumb-staff beam trawl
Side-scan sonarRiley push-net
Single-beam echosounderSeine
Split-beam sonarSemi-pelagic net trawl
Sub-bottom profilerSplit-beam trawl
Synthetic Aperture Sonars [SAS]Trammel bottom net
CorerTrap
Box corerAmphipod trap
Circular box corerFish trap
CorerModified crab pot
Craib corerPotting equipment
Diver (+corer)Recruitment cage
Diver (+ pipe corer)Trap
Diver (+ piston corer)Visual
Gravity corer360-degree camera
Gray O’Hare box corerBenthic video sled
HAPS corerBaited remote underwater vehicle [BRUV]
Hessler–Sandia box corerBRUV (+ stereo-video)
Modified Gray O’Hare box corerCamera
MulticorerDiver (+ photo)
Pipe corerDiver (+ video)
Reineck box corerDiver (+ visual)
Vibro corerDrop camera
DredgeHabCam bottom photos
Modified dredgeHybrid AUV
Modified scallop dredgeLagrangian floating imaging platform
Pipe dredgeMidwater video system
Triple-D dredgeMounted underwater cameras
GrabPhoto
Day grabQuadrats
Diver (+ manual dig)Remotely operated vehicle [ROV]
Double Van Veen grabROV (+ stereo-video)
Ekman grabSediment profile imaging [SPI]
Hamon grabSPI (+ plan view)
Mini-Hamon grabSPIScan
Shipek grabSubmersible
Smith–McIntyre grabTime-lapse photography
Ted Young-modified Van Veen grabTowed camera
Van Veen grabOnshore transect survey
Hook & LineOnshore visual survey
AnglingVideo
Surface longlineVideo sled
Trolling lineRemote Sensing
Vertical longlineLight Detection and Ranging [LiDAR]
Scrape SamplesOther
Diver (+ scraper)Clam rake
Free diver (+ scraper)Diver (+ depth logger)
Scrape sampleDiver (+ sampling)
PlatesFluorometer
Biofouling plateNet bag via diver collection
Settlement plateNiskin bottle + eDNA
Structure substitute (mesocosm experiment)Penetrometer
Table 4. Common analyses and software associated with the technology categories that had the most applications across habitats.
Table 4. Common analyses and software associated with the technology categories that had the most applications across habitats.
HabitatTechnology CategoryMost Common AnalysesMost Common Software
SeafloorAcousticBenthic terrain modeler, digital elevation modelR (raster), HYPACK®/HYSWEEP®, CARIS HIPS & SIPS™, QPS Fledermaus Software, ArcGIS®/ArcVIEW®
VisualCategorized by indices, PCA, generalized linear modelImage Analyst, BIIGLE 2.0, MATLAB, R, SigmaPlot
SedimentAcousticBenthic terrain modeler, digital elevation modelR (raster), HYPACK®/HYSWEEP®, CARIS HIPS & SIPS™, QPS Fledermaus Software, ArcGIS®/ArcVIEW®
Corer/Grab/DredgeANOVA, Tukey’s HSD post hoc, cluster, (n)MDS, ANOSIM, DISTLM, particle size analysis, PCAPRIMER, R (vegan, random forest)
VisualCategorized by indices, PCA, generalized linear modelImage Analyst, BIIGLE 2.0, MATLAB, R, SigmaPlot
InfaunaCorer/Grab/DredgeANOVA, Tukey’s HSD post hoc, cluster, (n)MDS, DIVERSE, SIMPER, SIMPROF, ANOSIM, DISTLMPRIMER, R (vegan, random forest)
VisualCategorized by indices, ANOVA, (n)MDS, DIVERSE, PCA, generalized linear model, SIMPROF, SIMPER, PERMDISP, PERMANOVAImage Analyst, BIIGLE 2.0, MATLAB, PRIMER, R, SigmaPlot
EpifaunaAcousticGeneralized linear model, generalized additive model, ANOVAEchoview Software, QPS Fledermaus Software, R, MATLAB
Net/DredgeCluster, ANOVA, Tukey’s HSD post hoc, (n)MDS, DIVERSE, SIMPER, SIMPROF, ANOSIMPRIMER
Plate/Scrape/VisualPCA, (n)MDS, PERMANOVA, PERMDISP, ANOSIM, ANOVA, SIMPER, generalized linear model, Mann–Whitney U-testsPRIMER, SigmaPlot, SPSS, EventMeasure Stereo, VLC media player, ImageJ
PelagicAcousticGeneralized linear model, generalized additive model, ANOVAEchoview Software, QPS Fledermaus Software, R, MATLAB
Plate/Scrape/VisualPCA, (n)MDS, PERMANOVA, PERMDISP, ANOSIM, ANOVA, SIMPER, generalized linear model, Mann–Whitney U-testsPRIMER, SigmaPlot, SPSS, EventMeasure Stereo, VLC media player, ImageJ
BiofoulingPlate/Scrape/VisualPCA, (n)MDS, PERMANOVA, PERMDISP, ANOSIM, ANOVA, SIMPER, generalized linear model, Mann–Whitney U-testsPRIMER, SigmaPlot, SPSS, EventMeasure Stereo, VLC media player, ImageJ
ANOVA = analysis of variance; ANOSIM = analysis of similarities; DISTLM = distance-based linear model; HSD = honest significant distance; (n)MDS = (non-metric) multidimensional scaling; PCA = principal component analysis; PERMANOVA = permutational multivariate analysis of variance; PERMDISP = permutational analysis of multivariate dispersions; SIMPER = similarity percentages; SIMPROF = similarity profile.
Table 5. Applicability to marine energy project sites of the most frequently used technologies for each of the six habitat categories. Multiple technologies were used across several habitat categories.
Table 5. Applicability to marine energy project sites of the most frequently used technologies for each of the six habitat categories. Multiple technologies were used across several habitat categories.
TechnologyHabitat CategoryUsed in High WaveUsed in High CurrentLimitationsUnwanted ImpactsCost *Analysis Software
Acoustic cameraPelagicYesYesWater turbidity and entrained air bubbles were noted to disrupt dataNone if frequencies used are out of hearing thresholds for sensitive organisms$35,000 to $85,000Manufacturer’s proprietary software or third-party software
ADCPPelagicYesYesWater turbidity and entrained air bubbles can disrupt data, as well as lack of particles in extremely clear water. None if frequencies used are out of hearing thresholds for sensitive organisms$5000 to $30,000Manufacturer’s proprietary software or third-party software
Beam trawlEpifaunaDependent on sea stateYesLimited capability on hard bottom (risks of net getting caught on rocks)Trawl contact with seafloor may leave deep scars$500 to $2500Any statistical analysis software
Box corerSediment
Infauna
Dependent on sea stateYes, but use is targeted for slack tides or lower flow conditions.Device weight needs to be sufficient to withstand currents and for adequate seafloor penetration; sediment characteristics will affect the ability of the technology to adequately collect samplesBow wave may displace flocculent material and mobile fauna may disperse$6000 to $55,000Any statistical analysis software
Day grabSediment
Infauna
Dependent on sea stateYes, but use is targeted for slack tides or lower flow conditions.Device weight needs to be sufficient to withstand currents and for adequate seafloor penetration; sediment characteristics will affect the ability of the technology to adequately collect samplesNone$5000 to $10,500Any statistical analysis software
Diver (scuba or free)Epifauna
Pelagic
Biofouling
Dependent on sea stateYes, but use is targeted for slack tides or lower flow conditions.High waves and current can impact safetyDiver motion may affect animals’ behavior$500 to $4500Any image & statistical analysis software
Drop cameraSeafloor
Sediment
Epifauna
Dependent on sea stateYes, but use is targeted for slack tides or lower flow conditions.High waves and current can impact stability; high turbidity impact image qualityAssociated lights may affect animals’ behavior$350 to $15,000Any image & statistical analysis software
Fisheries echosounderPelagicYesYesWater turbidity and entrained air bubbles can disrupt data; individual fish are hard to discern when they move in schoolsNone if frequencies used are out of hearing thresholds for sensitive organisms$38,000 to $300,000Manufacturer’s proprietary software or third-party software
Multibeam echosounderSeafloorYesYesRequires low sea-states to produce higher quality data; can be used in conjunction with other devices for more accurate data None if frequencies used are out of hearing thresholds for sensitive organisms$100,000 to $450,000Manufacturer’s proprietary software or third-party software
Photo (out of water)BiofoulingNot applicableNot applicableRequire structure to be pulled out of waterBiofouling communities are exposed to air<$2000Any image & statistical analysis software
ROVSeafloor
Epifauna
Pelagic
Biofouling
Dependent on sea stateYes, but use is targeted for slack tides or lower flow conditions.High waves and current can impact stability; high turbidity impact image qualityROV motion and lights may affect animals’ behavior$3000 to $6,000,000Any image & statistical analysis software
Scrape samplesBiofoulingYesYesHigh waves and currents can limit sample collectionDestructive sampling method but limited footprint<$20Any statistical analysis software
Sediment profile imagingSediment
Infauna
Dependent on sea stateYes, but use is targeted for slack tides or lower flow conditions.Image clarity affected by water turbidity; different sediment composition affects penetration depth and SPI may over-penetrate soft sedimentsNone$5000 to $90,000Any image & statistical analysis software
Side-scan sonarSeafloorYesYesRequires low sea-states to produce higher quality data, can be used in conjunction with other devices for more accurate data None if frequencies used are out of hearing thresholds for sensitive organisms$2000 to $45,500Manufacturer’s proprietary software or third-party software
Smith–McIntyre grabInfaunaDependent on sea stateYes, but use is targeted for slack tides or lower flow conditions.Device weight needs to be sufficient to withstand currents and for adequate seafloor penetration; sediment characteristics will affect the ability of the technology to adequately collect samples; may kite in deep waterNone$9000Any statistical analysis software
Sub-bottom profilerSeafloorYesYesEnergy loss/disruption as it propagates through high-energy water column can affect received data signalNone if frequencies used are out of hearing thresholds for sensitive organisms$12,000 to $160,000Manufacturer’s proprietary software or third-party software
Towed cameraEpifaunaDependent on sea stateYes, but use is targeted for slack tides or lower flow conditions.High waves and current can impact stability; high turbidity impact image qualitySled motion and lights may scare away mobile animals; sled contact with seafloor may leave scars$300 to $4000Any image & statistical analysis software
Van Veen grabSediment
Infauna
Dependent on sea stateYes, but use is targeted for slack tides or lower flow conditions.Device weight needs to be sufficient to withstand currents and for adequate seafloor penetration; sediment characteristics will affect the ability of the technology to adequately collect samples; high waves and currents can impact ability to get samples near an object or foundation.None$1400 to $13,500Any statistical analysis software
* Cost range estimates were based on publicly available information and multiple quotes for instrument purchase, which can be significantly reduced through rental options, and do not include additional expenses related to various instrument accessories, vessels and crews, labor, maintenance, and other ancillary costs.
Table 6. Technology recommendations for surveying epibenthic and demersal organisms (light grey lower matrix) and infauna organisms (dark grey upper matrix) at wave and tidal energy sites.
Table 6. Technology recommendations for surveying epibenthic and demersal organisms (light grey lower matrix) and infauna organisms (dark grey upper matrix) at wave and tidal energy sites.
Infauna
Epifauna
Strong CurrentsMild CurrentsHigh WavesLow/No WavesDeeper
30 m
Shallower
30 m
ObstructionsFree PassageCoarse SeabedSoft Seabed
Strong Currents DredgeDredge, heavy core, heavy grabDredge, heavy core, heavy grabDredge, heavy core, heavy grabDredgeHeavy core, heavy grabDredgeHeavy core, heavy grab
Mild Currents DredgeAny corer, any grab, dredge, SPIAny corer, any grab, dredge, SPIAny corer, any grab, diver, dredge, SPIDiver, dredgeAny corer, any grab, diver, dredge, SPIDay grab, dredge, Van Veen grabAny corer, any grab, diver, SPI
High WavesHook & lineFisheries echosounder, hook & line, trawl DredgeDredgeDredgeDredgeDredge-
Low/No WavesDrop camera, fisheries echosounder, heavy ROV, trawlAny ROV, divers, drop camera, fisheries echosounder, seine, towed camera, trawl Any corer, any grab, dredge, SPIAny corer, any grab, diver, dredge, SPIDiver, dredgeAny corer, any grab, diver, dredge, SPIDay grab, dredge, Van Veen grabAny corer, any grab, diver, SPI
Deeper 30 mDrop camera, fisheries echosounder, heavy ROV, trawlAny ROV, drop camera, fisheries echosounder, towed camera, trawlFisheries echosounder, hook & line, trawlAny ROV, drop camera, fisheries echosounder, towed camera, trawl DredgeAny corer, any grab, dredge, SPIDay grab, dredge, Van Veen grabAny corer, any grab, SPI
Shallower 30 mDrop camera, fisheries echosounder, heavy ROV, trawlAny ROV, diver, drop camera, fisheries echosounder, seine, towed camera, trawlHook & line, trawlAny ROV, diver, drop camera, fisheries echosounder, seine, towed camera, trawl Diver, dredgeAny corer, any grab, diver, dredge, SPIDay grab, dredge, Van Veen grabAny corer, any grab, diver, SPI
ObstructionsDrop cameraDiver, drop cameraHook & lineDiver, drop cameraDrop cameraDiver, drop camera DiverDiver, SPI
Free PassageDrop camera, fisheries echosounder, heavy ROV, trawlAny ROV, diver, drop camera, fisheries echosounder, seine, towed camera, trawlFisheries echosounder, trawlAny ROV, diver, drop camera, fisheries echosounder, seine, towed camera, trawlAny ROV, dredge, drop camera, fisheries echosounder, trap, trawlAny ROV, diver, drop camera, dredge, fisheries echosounder, trap, trawl Day grab, dredge, Van Veen grabAny corer, any grab, dredge, diver, SPI
Coarse SeabedDredge, drop camera, fisheries echosounder, heavy ROV Any ROV, diver, dredge, drop camera, fisheries echosounder, towed cameraDredge, fisheries echosounder, hook & lineAny ROV, diver, dredge, drop camera, fisheries echosounder, towed cameraAny ROV, dredge, drop camera, trapAny ROV, diver, dredge, drop camera, trap Any ROV, diver, drop camera, trapAny ROV, diver, dredge, drop camera, towed camera, trawl
Soft SeabedDrop camera, fisheries echosounder, heavy ROV, trawlAny ROV, diver, drop camera, fisheries echosounder, seine, towed camera, trawlFisheries echosounder, trawlAny ROV, diver, drop camera, fisheries echosounder, seine, towed camera, trawlAny ROV, dredge, drop camera, fisheries echosounder, trawlAny ROV, camera sled, diver, dredge, drop camera, fisheries echosounder, seine, towed camera, trawlAny ROV, diver, drop camera, trapsAny ROV, camera sled, diver, dredge, drop camera, fisheries echosounder, seine, towed camera, trawl
ROV = remotely operated vehicle; SPI = sediment profile imagery.
Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Share and Cite

MDPI and ACS Style

Hemery, L.G.; Mackereth, K.F.; Tugade, L.G. What’s in My Toolkit? A Review of Technologies for Assessing Changes in Habitats Caused by Marine Energy Development. J. Mar. Sci. Eng. 2022, 10, 92. https://doi.org/10.3390/jmse10010092

AMA Style

Hemery LG, Mackereth KF, Tugade LG. What’s in My Toolkit? A Review of Technologies for Assessing Changes in Habitats Caused by Marine Energy Development. Journal of Marine Science and Engineering. 2022; 10(1):92. https://doi.org/10.3390/jmse10010092

Chicago/Turabian Style

Hemery, Lenaïg G., Kailan F. Mackereth, and Levy G. Tugade. 2022. "What’s in My Toolkit? A Review of Technologies for Assessing Changes in Habitats Caused by Marine Energy Development" Journal of Marine Science and Engineering 10, no. 1: 92. https://doi.org/10.3390/jmse10010092

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop