Issue
Knowl. Manag. Aquat. Ecosyst.
Number 427, 2026
Freshwater ecosystems management strategies
Article Number 5
Number of page(s) 15
DOI https://doi.org/10.1051/kmae/2026001
Published online 02 February 2026

© M. Harwood et al., Published by EDP Sciences 2026

Licence Creative CommonsThis is an Open Access article distributed under the terms of the Creative Commons Attribution License CC-BY-ND (https://creativecommons.org/licenses/by-nd/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. If you remix, transform, or build upon the material, you may not distribute the modified material.

1 Introduction

The development of effective and feasible long-term monitoring programmes is crucial to identifying key drivers of large-scale environmental degradation and determining the efficiency of potential restoration (Lindenmayer and Likens, 2010). In situ, multi-dimensional observation data achieved through field monitoring can be used to link key processes and biological responses such as community composition, population dynamics, breeding ecology, foraging rates, behaviour and response to stressors at a landscape scale (Block, 2005; Caravaggi et al., 2017; Lindenmayer et al., 2022). Signals of large-scale biological change may only be detected after multiple sampling seasons and these changes may be non-monotonic, for example, boom-bust dynamics of non-native invasive species and native species population responses (Haubrock et al., 2022; Lindenmayer et al., 2022). Well-designed monitoring programmes thus need to encompass both long-term and landscape-scale processes, which means that they are extremely resource-intensive in terms of both cost and people time (Lindenmayer et al., 2022). During the current rapid rate of environmental change, finding solutions to overcome these challenges is critical for biodiversity managers to answer key ecological questions, determine long-term changes, provide robust evidence to guide management actions and unequivocally demonstrate the benefit of any intervention investment.

Freshwater ecosystems are facing a biodiversity crisis with freshwater vertebrate populations declining twice as fast as terrestrial or marine populations (Tickner et al., 2020). Monitoring programmes in aquatic environments not only face struggles regarding time and cost, but also require specialised equipment and training. Traditional aquatic survey methods (e.g., trawling, gill nets, electrofishing, trapping) tend to be extractive, destructive and have inherent biases which may produce an inaccurate representation of a given population (Cappo et al., 2006; Cooke and Schramm, 2007). In addition, capture methods, such as catch and release, can elicit behavioural changes which impact fitness. An example of this being the nest abandonment behaviour observed by male black bass (Micropterus spp.) after catch and release surveys that leads to the total loss of offspring (Hanson et al., 2007). In situ snorkel surveys can be completed to reduce negative animal impacts of capture, but these are biased by observer ability, water conditions and fear responses to the observer therefore, extractive methods are used in tandem to maximise reliability (Weyl et al., 2013; Ebner et al., 2015). Environmental DNA (eDNA) approaches are being increasingly utilised and presented as a solution to aquatic ecosystem sampling limitations (Beng and Corlett, 2020). However, molecular analysis is costly and conclusions based on eDNA are currently restricted to detecting the presence/absence of species with available barcodes, and inferences may be spatially confounded in lotic systems due to downstream transport of genetic material (Beng and Corlett, 2020). Even if analysis advances to the point where eDNA surveys can accurately estimate total abundance or biomass, it would not be able to observe the size structure of the populations, which is an important metric for fisheries. It is also noted that neither capture-based methods nor eDNA allow for in-situ behavioural studies.

Camera traps and remote imaging have been extensively used in terrestrial ecosystems as they increase observation likelihood of larger and rare species and remove negative impacts of capture-based methods (Feyrer et al., 2013; Caravaggi et al., 2017; Delisle et al., 2021). Aerial surveys have been used in terrestrial and marine environments to monitor large mammals, fish, and plant stands, by tracking movement and population sizes, but they are limited by weather conditions and to animals or plants that are not hidden beneath water or tree canopies (Kelaher et al., 2019; Camacho et al., 2023). Remote imaging methods remove the risk of sampling in locations that are inaccessible or unsafe (Harvey et al., 2013; Chaudoin et al., 2015). Furthermore, results can be quickly validated by reviewing video data, unlike eDNA and aerial surveys, which often need ground-truthing, and datasets are archived for future reference and analysis, thus making it ideal for long-term monitoring programmes looking to maximise data collection (Hitt et al., 2021).

In aquatic systems, above-surface cameras have been used to monitor Atlantic salmon (Salmo salar) farm escapes, species assemblages, migration patterns and barriers (Shortis and Otis, 2014; Morán-López and Uceda-Tolosa, 2017; Morán-López and Uceda-Tolosa, 2020). Technological advancement, such as waterproof camera housing able to withstand high pressure, has facilitated the application of Remote Underwater Video (RUV) systems. Use of RUV and Baited RUV (BRUV) has been applied broadly in marine systems and is now a common part of the marine fisheries assessment toolkit as they provide fishery-independent data which is efficient, low-cost, and comparable across locations (Mallet and Pelletier, 2014; Whitmarsh et al., 2017). However, the application of remote underwater video in freshwater lags behind that in marine environments despite the potential for innovative monitoring.

The purpose of this review is to synthesise the current literature on the application of RUVs in freshwater and recommend a standardised methodology for effective and comparable monitoring efforts. Where possible we have identified the methods and objectives of freshwater RUV studies and categorised them according to the study objectives. In doing so, we provide a roadmap for using RUVs in freshwater aquatic systems. We also provide a starting point to advance freshwater RUVs' best practices to ensure robust data collection and enhance scientific development while addressing critical knowledge gaps in conservation and fisheries science.

2 Methods

A comprehensive systematic literature search was conducted using the Institute of Scientific Information (ISI; Thomson Reuters) Web of Science online database and Google Scholar database. These databases were searched to find any literature that contained relevant information regarding RUVs in freshwater published up to December 2024. The search term included a range of keyword combinations (Tab. 1). The guidelines for Preferred Reporting Items for Systematic reviews and Meta-Analysis (PRISMA) (Page et al., 2021a; Page et al., 2021b) were used to report this systematic literature review. The results obtained were collected and assessed by a single reviewer.

Each publication returned was examined and included if it involved using RUVs in a freshwater environment. For each publication, we recorded the following (if details were available); What was being measured/observed in the study, the year of publication, the country the study was undertaken in, the focus species of the study, the waterbody type that the study was conducted in, and the methods used. After reviewing each of the returned pieces of literature, a backward snowball of references was conducted to check for any further relevant literature, which was then incorporated into the database (Wohlin, 2014). Each of these studies were then categorised by the focus of the study. Literature, which was relevant but did not consist of a specific measurement/observation, was also noted and explored further for information that was relevant to this review.

Table 1

Keyword combinations used in initial literature search.

3 Results

A total of 185 unique pieces of literature were identified through database searching, backward snowballing and personal correspondence (Fig. 1). The first published literature on freshwater applications of RUVs was in 1988, which documented swim-up and downstream movement of newly emerged Sea Trout (Salmo trutta) fry in the River Itchen, UK (Moore and Scott, 1988). Annual publications were sporadic and in small numbers until 2014 when there was a sharp increase in publication rate (Fig. 2). The database search returned studies undertaken in 27 different countries, spanning all six inhabited continents.

thumbnail Fig. 1

PRISMA flow diagram illustrating the different phases of the systematic literature review data identification and inclusion.

thumbnail Fig. 2

Histogram of literature related to RUVs in freshwater released each year.

3.1 Survey design

Method specificity and reporting standards are needed for reproducible and comparable RUV research. Despite this, two thirds of the literature did not include information on at least one of these factors (Tab. 2). Prior to 2014, most studies used expensive professional cameras. Since 2014, most RUV studies in freshwater have used some form of action camera. A broad range of frame rates were returned by the literature search (Tab. 2). These ranged from a time lapse video of 1 frame every 5 s to capture habitat use by threatened species (Hannweg et al., 2020a), to a slow-motion video recording at 240 fps trying to capture biomechanics of foraging (Moran et al., 2019). Most studies returned by the literature search did not account for any acclimation time between the initial deployment of the RUV and recording results (Tab. 2).

Remote Underwater Videos with bait arms attached (BRUVs) within the camera's field of view to attract individuals was a common customisation (20% of surveys used some form of baited arm). Bait material and volume was varied, including: bread and marmite, cat food, freshwater fish carcasses and fish eggs (Sup Mat).

The duration of deployments varied greatly. Deployment time is listed as the duration of a single camera deployment, some studies conducted multiple short deployments across multiple microhabitats, whereas others used a single deployment at one site for an extended time. When the RUV is used for a rapid deployment and not left continuously recording the most common duration (12%, n = 22) was for 60 minutes and the second most common duration (8%, n = 14) was for 30 minutes. Other durations have been used in a more sporadic distribution, with the longest, none-continuous single deployment lasting for 960 minutes (Holubová et al., 2019).

with camera battery life and limited budgets and tight deadlines, and results being required from a single season of surveying, playing a key factor in this.

A range of different video analysis methods were employed throughout the literature. The most common method (58%, n = 108) was by a human reviewer watching the footage and manually noting observations. The other method involved the use of specialist software, e.g., EventMeasure (seagis.com.au), Everfocus (everfocus.com), Beast Software (beast.community), Argus (argussoft.org) and Tracker 5.1 (physlets.org) to review footage (13%, n = 24). These softwares range in complexity and cost.

Table 2

Prevalence of technology and methods reporting in the literature.

3.2 Abundance

Assessing species abundance is a critical component of conservation and wildlife management. This was the most common application of RUVs with 36% (n = 64) of studies aiming to determine relative or total abundance of aquatic biota.

The most frequently used method (66%) is calculating the maximum number of individuals, of a single species, observed simultaneously in a single frame known as MaxN (Hitt et al., 2021). This value can be determined by either searching fixed time points (i.e., every 30 seconds) for a frame with the most individuals of a target species recorded (Hannweg et al., 2020b) or obtained by reviewing the entire video (Crook et al., 2021). Alternatively, SumMaxN, a cumulative sum of the MaxN for every species can be used to determine fish abundance within a given habitat or area (Work and Jennings, 2019). If duplicate counting of animals was not considered a confound, e.g., fish passing through a one-way fish pass (Johnson et al., 2007), counting the total number of fish observed (25% of records) was used to estimate species biomass by either estimating the densities and percentage-cover of target species (Karatayev et al., 2021) or using video quadrants (Andres et al., 2020).

3.3 Species richness

Identifying species richness and diversity usually relies on being able to physically handle an animal to key it out correctly or through eDNA analysis, which is compromised in tropical localities by limited barcode libraries and cryptic species. RUVs may offer an alternative to species richness and biodiversity assessments. Overall, 24% (n = 44) of studies utilised RUVs for this task with 83% either reviewing the footage in full (Glassman et al., 2022), or by selecting a random frame every minute (Robinson et al., 2019) to identify all individuals to species level and create a species list. Generally, the quality of the video allowed species to be identified to species level by experts and through consulting identification guides for diagnostic characteristics (van Wyk et al., 2017; Pedersen, 2021). In some instances, differentiation between similar species can be confounded due to visibility issues and cryptic taxonomy (Cooke and Schreer, 2002; Widmer et al., 2019). Therefore, identifying organisms to family level occurred in 11% of publications.

3.4 Spawning/mating/nesting

Studying reproductive behaviour of aquatic biota without causing adverse impacts on the target species is fraught with difficulties. RUVs were used in 16% (n = 30) of studies where 74% deployed RUVs at known spawning sites to confirm event timings. In some cases, this was used as a solution to better understand spawning of critically endangered fish such as the Devils Hole Pupfish (Cyprinodon diabolis) (Chaudoin et al., 2015). Furthermore, RUVs can visually assess effects of abiotic factors such as habitat (Groves and Chandler, 1999) and the lunar cycle (Fernández et al., 2021) on salmonid spawning. RUVs can also be used in tandem with hydrophones to expand the toolkit of remote sensing in aquatic habitats; for example, a novel method of time-synchronised sound and video was also used to identify the sounds produced by spawning trout (Johnson et al., 2018). Opportunistic sampling was able to document footage of courting and mating behaviour incidentally during recording. One of these studies provided the first observation of copulation of the cryptic Andean Catfish (Mena-Valenzuela et al., 2022). Another observation was courtship of Zebrafish (Danio rerio) which was recorded outside of the known mating season by chance in a separate RUV study (Sundin et al., 2019). RUVs were positioned directly in front of the nests of target species to observe nesting behaviour. Behaviours ranged from nest guarding and maintenance behaviours conducted by males (Unger et al., 2020), to interactions with heterospecific species eggs placed within the nest (Yamane et al., 2016), subordinates within nests, sheltering with juveniles, and cooperative breeding (Satoh et al., 2022). One study used a less targeted approach where RUVs were deployed in the USA to opportunistically record nesting of Redbreast Sunfish (Lepomis auratus) (Martin and Irwin, 2010).

3.5 Behaviour

Behavioural studies comprised 14% (n = 25) of the literature, where responses to external stimuli including anthropogenic sounds (Fleissner et al., 2022), chemical cues such as chemical predatory alarm cues (Friesen and Chivers, 2006), infrared lighting (O'Malley et al., 2018) and researchers shadows (Smith, 2022) formed the majority of the analysis. Beyond that, general behavioural time budget research, such as time spent swimming compared to nesting or foraging was the core focus of these papers. RUVs were used to quantify the extent of inter and intraspecific interactions, for example territorial defence behaviours in fish (Ebner et al., 2017), aggressive interactions between noble crayfish (Astacus astacus) individuals within the same trap (Raugstad, 2019), and competitive interactions between invasive and native crayfish species (O'Hea Miller et al., 2022a). Collective behaviour of fishes was assessed through open water RUV deployment, where a focal species was identified but data collected on the icthyofaunal community as a whole.

3.6 Migration

Migration studies comprised 10% (n = 18), where 56% of this subset deployed RUVs into obstacles passed by migrating species including fish ladders (Negrea et al., 2014), fishways (Limaye, 2019), weirs (Marston, 2014) and fish passes (Hawkins et al., 2018). These RUVs were deployed primarily for commercially important species Alewives (Alosa pseudoharengus), Rainbow Trout and Sockeye Salmon (Oncorhynchus nerka). The RUVs were left to continuously record, and the footage was reviewed to count the total number of individuals that passed either upstream or downstream. In some cases, a priori knowledge of important migratory locations were chosen for RUV deployment whereas in others, RUVs were deployed at waterbody entrances of specialised migration swim-through chutes to monitor salmonid migration (Musslewhite, 2020). Finally, multiple camera arrays of RUVs were strategically placed along the Atlantic Salmon migration route to incorporate the spatio-temporal aspect of migrating populations (Borgstrøm et al., 2010).

3.7 Foraging

Foraging activities comprised 7% (n = 13) of the overall results. These recordings provided information on trophic interactions to quantify intensity of bottom foraging (Pledger et al., 2014), feeding aggregations (Starrs et al., 2015) and species feeding on floating material including zooplankton (Marchand et al., 2002) and recently released eggs (Šmejkal et al., 2017). Baited studies comprised 31% (n = 4) with the intention of observing scavenger feeding behaviour with the most common bait being a fish carcass positioned in front of the RUV (Unger and Hickman, 2019). High frame rate video was used to record predation events by Bluegill (Lepomis macrochirus) on live prey tethered within view of the RUV (Moran et al., 2019).

3.8 Size

Estimating length underwater of a moving object is a barrier to ascertaining critical fisheries data, thus length frequency studies made up 7% (n = 13) of the total results. The most common method (62%) estimated size by comparing an individual to an object of known size that is within the frame of the video. These objects were variable and included a stake of known size (Tweedie et al., 2018), to specially mounted scale bars (Loffredo, 2018). In some instances, exact sizes were not calculated, instead individuals were either assigned a size class bin (Hopper, 2019) or estimated in relation to previously caught individuals (Skorulis et al., 2021). Specially calibrated stereo-RUVs and specialist software was used in 18% of studies to accurately estimate the size of individuals. One novel method was applied in Canada to study Shortnose Sturgeon (Acipenser brevirostrum), where parallel lasers were mounted to an RUV and used to estimate length (Usvyatsov et al., 2012). Another novel method involved counting the pixels a fish took up in footage when it passed a known location and transforming these to millimetres to estimate sizes, as done in Reunion Islands to estimate the size of Red-tailed Goby (Sicyopterus lagocephalus) (Boussarie et al., 2016).

3.9 Habitat use

RUVs were used to assess habitat associations in 7% (n = 13) of the results. Most studies aimed to determine differences in artificial habitat use compared to natural habitat as well as assessment of seasonal habitat changes (Pratt et al., 2005; Lintermans et al., 2013). RUVs were also used to quantify cyprinid habitat use after disturbance events from hydropeaking (Boavida et al., 2021).

3.10 Presence

A small number of studies (5%, n = 10) were intended to confirm species presence in a waterbody. Most studies deployed RUVs at a fixed location within the waterbody in the hope of serendipitously detecting a species, such as the first official record of the Cleft-lipped Goby (Sicyopterus cynocephalus) in Australia and multiple deployments were used to determine the presence of escaped farmed salmon in Norway (Ebner et al., 2017; Svenning et al., 2017). Macrophyte studies were rare across the dataset but short RUV deployments were completed in multiple locations in the UK to confirm the maximum colonisation depths of all macrophytes in the waterbody (Spears et al., 2009).

4 Case study applications for fisheries science and conservation

4.1 Conservation intervention

Eradication of non-native invasive species is a high-risk, high-cost venture which relies on robust evidence-gathering and success post-intervention. A successful example of an invasive fish eradication project took place at the Rondegat River in the Cape Fold Ecoregion, South Africa (Marr et al., 2012; Weyl et al., 2013; Weyl et al., 2014; Weyl et al., 2016), an important biodiversity hotspot characterised by high diversity and endemism (Ellender et al., 2017; Broom et al., 2023). RUVs were deployed yearly to effectively monitor the recovery of the endemic fish population in a non-destructive manner (Weyl et al., 2013; Weyl et al., 2014; Weyl et al., 2016). Using the Rondegat River's RUV yearly dataset (2011–2016), Castañeda et al. (2020) tracked the occupancy dynamics of the endemic fishes along the river, before and after the eradication of the invasive fish. They found that the strongest driver of the endemic fish's probability of occupancy in the river was the presence of an invasive fish. After the invasive fish eradication, the endemic fish were able to naturally colonise downstream sections of the river and increase in density. Two of the endemic fish populations appear to have reached population equilibrium across the river, while the third has not, suggesting it may be more sensitive to fluctuations in habitat variables (Castañeda et al., 2020). To assess the habitat associations of the three vulnerable and recovering cyprinid species, Broom et al. (2022) utilised a RUV system across 51 sites as part of a long-term monitoring project for the Rondegat River post-intervention. With repeated sampling over three seasons (2018–2019), Broom et al. (2022) were able to assess community composition and relative abundances with respect to habitat, its overlap with a protected area and species-specific abiotic predictors of relative abundance. Results confirmed a lack of re-invasion and indicated that habitat-specific interventions to reduce the impact of drought, eutrophication and sand deposition are needed along the Rondegat River to ensure the continued persistence of threatened fish. Underwater video monitoring is an effective and low-cost approach that can rapidly inform tangible conservation recommendations for vulnerable fish species in impacted or recovering river systems, especially in locations with underfunded resourcing for biodiversity management.

4.2 Ethology

O'Hea Miller et al. (2022a) investigated the competitive interactions and outcomes between an invasive crayfish (Cherax destructor) and a critically endangered native one (Euastacus dharawalus), which cohabit a 7.5 km stretch of creek in Wildes Meadow, located in the Southern Highlands region of NSW, Australia. Up until this point, behavioural investigations of invasive and native crayfish had largely been confined to laboratory trials, which facilitate clear and controlled observations of individuals competing over resources (Cerato et al., 2019; Lopez et al., 2019; O'Hea Miller et al., 2022b). Owing to the challenges of observing individuals in situ, particularly due to shallow and often turbid conditions, little was known about how these species interacted under natural conditions nor whether body size affected contest dynamics and outcome. By deploying 15 baited remote underwater videos along nine locations within the creek over the course of 12 months, O'Hea Miller et al. (2022a) were able to extract and score 178 interspecific and intraspecific interactions from which interaction duration, maximum intensity, conclusion, outcome, and interaction initiator were quantified. All behaviours were assessed relative to an established ethogram (Bergman and Moore, 2003) and relative body size of contestants was estimated from the precent difference in size as measured on the video screen (Martin and Moore, 2007). Overall, Euastacus dharawalus won more contests than the invasive species Cherax destructor; however this was largely attributed to the fact that in most cases, E. dharawalus was larger than C. destructor. Alarmingly, when considering only interactions where contestants were size-matched (i.e., within 10% body size), C. destructor was more likely to win interactions than E. dharawalus. Additionally, C. destructor were more willing to initiate contests than E. dharawalus, even if C. destructor was the smaller contestant, and they were more willing to continue fighting than E. dharawalus in intraspecific contests, demonstrating a greater inherent aggressiveness of the invasive species. This study highlights the capacity of BRUVs to quantify complex behavioural interactions in challenging freshwater systems, but also a key consideration of using BRUVs for behavioural studies – namely the potential for limited and unbalanced sample sizes. Firstly, some BRUV deployments had to be discarded from the analyses due to high turbidity and time of year (i.e., winter crayfish inactivity). Secondly, O'Hea Miller et al. (2022a) reported only one interaction where E. dharawalus was smaller than C. destructor (compared to 29 interactions where C. destructor was smaller than E. dharawalus). Future considerations must, therefore, involve increasing the number of BRUV deployments over time and the use of stereo-BRUVs to enable scoring of relative body sizes of all individuals in the frame. Both these considerations will help boost replication of behavioural observations and hence the efficacy of BRUVs for understanding behaviour in freshwater systems. Incorporating ethological studies and interspecific interactions into fisheries management plans has been a persistent and key challenge which may be tackled by appropriate use and deployment of BRUV systems.

4.3 Fisheries monitoring

Chambo (Oreochromis spp.) is a key fishery in Lake Malawi and is a key target for management and conservation efforts. However, traditional monitoring methods for Chambo, such as gillnetting and trawling, are destructive and can negatively impact fish populations (Tweddle and Magasa, 1989; Banda et al., 2005; Weyl, 2005; Weyl et al., 2010).

Van Wyk (2019) evaluated the potential for using stereo-BRUVs to monitor Chambo populations across different management zones of Lake Malawi (Mozambique and Malawi) to determine the optimal sampling design for annual monitoring. Both Chambo abundance and size differed significantly between Malawi and Mozambique - which may be attributed to differences in fisheries pressure. Malawi experiences greater levels of fishing pressure compared to Mozambique, resulting in a decline in Chambo populations and a decrease in the size of sexually mature individuals. In contrast, Mozambique has relatively low fishing pressure due to low population densities, weak market forces, and a history of civil war. This has resulted in higher Chambo abundance and larger sexually mature individuals in Mozambique compared to Malawi (Halafo et al., 2004; Weyl, 2005; Weyl et al., 2010; van Wyk, 2019). In this system, an acceptable stereo-BRUVs deployment time was 15 minutes and required a maximum of 120 annual video samples to detect a 10% change in Chambo abundance over a hypothetical 10-year monitoring scenario. This suggests that stereo-BRUVs can be used as a cost-effective long-term monitoring tool for economically and ecologically important fisheries, provide evidence-based recommendations for the establishment of closed sanctuary areas, and monitor intervention outcomes.

This case study highlights the importance of effective, standardisable monitoring methods for fisheries management and conservation, and the potential of stereo-BRUVs technology to provide robust data for monitoring and managing complex inland fisheries.

5 Discussion

Despite RUV research being completed across a broad range of subject matter and spanning continents, there is a distinct lack of cohesion in method standardisation between research groups. This is a stark contrast to the marine environment, where proven methodological standards are in place and coordination levels at a global scale are high. The lack of standardisation within the freshwater environment limits the potential comparisons between studies or meta-analyses, thus hampering RUV work being used to its full capacity in freshwater fisheries. Research so far has, therefore, been fairly ad-hoc, with a sharp increase in the literature published annually from 2014, which likely reflects a technological trend in better video quality, combined with a decrease in the cost of cameras, which has made action cameras more available. The drop in frequency of literature using freshwater RUVs between 2021 and 2022 is believed to be a result of COVID-19 lag in publishing, with limited studies occurring during the pandemic lockdowns. However, there does not appear to have been a rebound in the volume of annual publications and the number of publications each year post 2020 have remained stable. Several studies have used historical data that is older than 5 years, while others do not specify the timeframe of data collection. Analysis protocols, such as human reviewers watching 100+ hours of footage to obtain a complete species list, will be more time consuming than video analysis that automatically identifies the presence of an individuals through Artificial Intelligence. Overall, the processing delay between data collection and publication is entirely reliant on the resources available and the questions that are being asked.

5.1 Use of RUVs

Freshwater research utilising RUVs has the capacity to be a one size fits all method for ecological assessments and fisheries science, if deployed correctly and in a standardised manner. Development of a freshwater RUV consortium following a standardised methodology could result in globally coordinated research which spans broad spatio-temporal ranges with the capacity to answer pressing questions in fisheries science. Similar consortiums have been created, for example: acoustic tracking in marine systems and BRUV census of global shark populations, which have resulted in unexpected natural history observations (Phillips et al., 2019; MacNeil et al., 2020; Lennox et al., 2024). As RUVs represent a long-term low-cost data acquisition method they are an excellent tool for post conservation intervention monitoring, as once the initial costs of purchasing the equipment are covered, future costs are limited to staff cost, travel cost and data storage and processing (Harwood et al., 2025). They can also be used to complete rapid baseline assessments of freshwater environments, perform freshwater fisheries stock assessments or monitor the escapements of farmed fish (Weyl et al., 2013; Svenning et al., 2017). This is especially true for stereo-B/RUVs which provide accurate length estimates for length frequency and biomass estimations which can be used to support fisheries independent assessments.

5.2 Limitations of RUVs

With most modern action cameras maximum battery life is around 80 minutes, however, this can be lower in colder waters, meaning that RUVs with action cameras cannot be deployed for extended periods of time, which can result in key events being missed. Other issues include malfunctioning memory cards, water damage, unfocused images and obstacles within the field of view, all of which can result in wasted effort (Struthers, 2015). Although depending on the specific set up of the rig, i.e., commercial or home-made, there may be low-tech ways to mitigate these, with low-cost extended battery life camera system being developed (Magneville et al., 2023; Fetterplace et al., 2023; Dunkley et al., 2023). There are also environmental limitations into RUV surveys, such as light levels and turbidity limiting data capture. Turbid water greatly reduces an RUVs field of view which reduces probability of event observation. Similarly suitable lighting and hours of daylight restricts timing of many surveys and introduces bias against nocturnal species - which may also avoid artificial lighting (Struthers et al., 2015). This highlights a priority question to advance methodology by assessing the effectiveness of white, red and blue lights for RUV surveys.

5.3 Camera setup and analysis

A set of standards for using stereo-BRUVs in marine environments has been proposed (Langlois et al., 2020) and these have been used as a framework to guide the standards described here, to ensure reliable deployments of all forms of RUVs in freshwater. To be able to create a standardised method for RUVs in fisheries research there are several systematic methodological developments that need to be considered (Tab. 3).

Any action camera which can record at the recommended settings can be used for future standardised surveys. Framerate, resolution and field of view (FOV) are all important considerations as they influence a video analyst's ability to accurately identify, count and measure fish, as well as the size of the visible area (in the case of FOV). At a minimum, high definition (1920 × 1080p) resolution with 30 frames per second, with a field of view between 109° and 120°, appear to be an adequate standard (Langlois et al., 2020). While 4K resolutions might be tempting, researchers will run into challenges with cameras overheating and space for data storage. For measuring fish length with stereo-camera any settings that automatically adjust the pixel size (e.g., image stabilisation), frame rate (e.g., auto low light) or distort the image (e.g., fish-eye or ultra-wide FOV) should be disabled (Langlois et al., 2020). Standardisation of survey areas can be achieved through the placement of quadrats of known size on the bed of the waterbody, within the camera's field of view (Longo et al., 2018).

Acclimation time is likely to vary between species and communities depending on their exposure to disturbance and life history traits. Most studies reviewed here did not include an acclimation time as most species entered the RUV's field of view a short period of time after deployment. This is a methodology priority question - to determine a suitable baseline acclimation time for different species and purposes to ascertain whether a standard can be achieved. Similarly, a standard operating procedure for total deployment time has not yet been determined, thus we recommend the most common deployment duration time, i.e., 60 minutes. However, van Wyk (2019) found that 15 minutes was sufficient for fisheries monitoring in Lake Malawi, whereas 60 and 30 minutes is a recommended deployment time in marine systems to reduce diminishing returns (Langlois et al., 2020). Sampling efficiency analyses such as time - species accumulation curves in freshwaters are required urgently.

Video analysis by Artificial Intelligence is in development, this AI would be able to identify frames of the footage that hold a target species that can then be analysed by a human reviewer. Artificial Intelligence has been used for the automated identification of marine fish and invertebrates (Bürgi et al., 2025), but large training datasets are required in order to achieve these results (Ditria et al., 2020). For Artificial Intelligence to be successful in freshwater environments these large training datasets are an area for future work. Potentially, in the future there is even the scope that it can fully review footage identifying all species and individuals that occur throughout a video sample, but prior to optimisation and validation of these models human review should be prioritised. Ideally, reviewers will have undergone species identification and software training prior to analysis. Random review should be implemented for quality assurance, and if a complex community is present then two independent reviewers should be used to ensure accuracy. While human review is currently the only viable option, researchers should invest effort into developing training datasets to enable AI applications when the technology is mature.

Compared to RUVs, BRUVs achieve higher MaxN and species richness estimates. Therefore, BRUVs should be used for abundance, species richness and presence absence studies. Due to bait-attraction altering natural behaviour we do not advise their use for ethological observations or habitat use, nesting and migration. On the other hand, BRUVs can be used effectively for some ethology experimental purposes such as scoring competitive behaviours and aggression (O'Hea Miller et al., 2022a).

Experimental bait efficiency assessments need to be completed to recommend a data-driven standard, where bait type, volume, local hydrology and survey purpose must be considered. Using a bait local to the area is recommended for practical purposes, small oily food fish species work well as the scent plume travels well in the water, and they are usually inexpensive and readily available. The use of local fish reduces the risk of the introduction of disease or invasive species while conducting surveys. Nonetheless, non-natural bait has also been used, e.g., marmite™ and bread (Bajaba et al., 2021), variations of this, or indeed canned oily fish may be preferable if surveying in remote locations. The use of marine species as bait in freshwater has been promoted in the UK during crayfish surveys to reduce chances of disease introduction through freshwater bait (J South pers. com.). Furthermore, depending on survey location, safety concerns should also be considered when using BRUVs as bait has been known to attract large predators, like crocodiles, that pose a risk to researchers and BRUVs should be avoided when these risks are present (King et al., 2018). Effort should be applied to follow FAIR (Findable, Accessible, Interoperable and Reusable) data workflows to the large amount of data produced in RUV surveys (de Visser et al., 2023). This study has highlighted that more than 10% of all studies are missing details about protocols, illustrating that more needs to be done to meet the FAIR data workflow requirements for detailed metadata about protocols.

As standard, all data should be suitably annotated with meta-data for location, date and surveyor, and saved in raw video format. Good practices regarding data management and storage are crucial and data ought to be stored along with off-site back-ups in both physical and cloud repositories. However, this may incur unforeseen costs for practitioners and researchers. We strongly recommend the creation of a global freshwater RUV repository, following open data principles, similar to those suggested for marine systems (Langlois et al., 2020). Standard approaches to analysis will enhance the usability and interoperability of datasets and analysis codes. All species should be identified to the lowest taxonomic level possible. MaxN analysis methods should be used as standard in abundance studies, as it is less likely to overestimate true abundance (van Wyk, 2019). Efficiency and robustness of MaxN calculation approaches, such as snapshots vs total video, need to be assessed to recommend best practice. MaxN may underestimate abundances if there are instances of several groups of individuals, newly proposed Synchronised MaxN (SMaxN) could offer a more accurate estimate when videos include several groups of individuals (Magneville et al., 2024). Specialist software, such as EventMeasure, can be used to annotate video which can ensure that fish are not counted multiple times or missed when reviewing footage to reduce the risk of miscounts when calculating MaxN values. This software can also be used with stereo-RUVs to obtain accurate fish lengths after careful calibration (Langlois et al., 2020). When possible, specialist software should be used to ensure that results are consistent; however, the high costs of licences for this software often makes it implausible. Regardless of the use of specialist software, the suggested standard methods should be used when reviewing footage, with footage saved for future review if requested. Behavioural studies should follow published ethograms when possible, however, the reviewing process can be lengthy and subject to observer bias. Using free software such as BORIS (Friard and Gamba, 2016) the recommended standard method of analysis would be to review footage back at an increased speed, until a desired event is observed, and then reviewing the footage at normal speed to score results, as in O'Hea Miller et al. (2022a). Automated behavioural analysis software is available, but the cost is often prohibitive for environmental managers and negates the initial RUV cost saving.

Table 3

Recommended standards and reasoning.

5.4 Future steps and potential developments

The prospect of low cost, high data acquisition methods for fisheries monitoring and management means that technology is constantly developing for both research and commercial applications. Novel methods including a Raspberry-Pi platform can allow automated data acquisition through scheduling and automatically uploading results to an online database (Almero et al., 2021), or through a video streaming link that listens for requests to connect (Dadios et al., 2022), removing the need for researchers to replace batteries and storage cards. This technology is in the initial trial stages and currently the video is limited to 6 fps, which does not adhere to the standards suggested.

Time spent reviewing footage is a major bottleneck in RUV methodology, this may be overcome with optimisation of artificial intelligence applications and machine learning to automate the process. Through deep-learning, AI can be trained to categorise behaviours and identify fish species with the most recent versions being able to detect fish and categorise species to almost a human-like accuracy (Abangan et al., 2023). Approaches such as Convolutional Neural Networks or the You Only Look Once (YOLO) algorithm can be optimised to identify species passing through fish passes or in RUV footage to automatically identify species (Ovalle et al., 2022; Soom et al., 2022). For instances when species identification is not plausible AI, could be used instead to flag instances when individuals are present on the screen so that a human observer can manually review a smaller subsection of the video file with confirmed presence, rather than reviewing footage without species present. Furthermore, this could be developed further to enable the monitoring and tracking of individual fish over time, calculate rapid biomass estimated by deriving length-weight relationships, and expedite the accurate detection of invasive fish through catchments, thus potentially revolutionising the way we monitor and manage aquatic ecosystems. Environmental factors including turbidity and lighting limit the effectiveness of RUVs, specialist lighting rigs can be developed to address lighting issues; for example, a clear liquid optical chamber to improve underwater visibility (Jones et al., 2019).

Remote Operated Vehicles are a move away from the static camera approach and should be considered a separate methodology entirely, with method development focused on in their own right. These have almost exclusively been used in marine environments but are increasingly being exploited in commercial applications in freshwater. For example, ROVs have been deployed effectively in reservoirs to assess the presence and distribution of target species, such as Signal Crayfish (Pacifastacus leniusculus) (P.D. Stebbing pers com.). Information gathered from such surveys has facilitated determining the risk of spread of invasive non-native species from reservoir assets and their distribution within the asset providing valuable information for the development of biosecurity and management plans. Additionally, ROVs are able to detect signs of crayfish, such as burrows, burrow bound animals, and parts of animals, such as claws and carapaces, which trapping or static video may miss. This provides much more detailed information on the size and distribution of the population, in addition to key information on meta-population distribution, which is vital in the development of management plans. The deployment of traditional monitoring methods, such as trapping for crayfish, are not suitable for assessing key locations in reservoirs which are often hard and dangerous to access. Draw off towers and scour values present key points of risk for the potential dispersal of invasive non-native species from impounded reservoirs but are difficult to monitor due to health and safety risks presented by the infrastructure and its operation, in addition to the depth of water in which they are often situated. As ROVs can be deployed at a distance and at depth, with umbilical cords of 100 m being common, these issues are overcome. The large size and weight of currently available ROVs does not make them an ideal tool for monitoring smaller freshwater environments. While ROVs are becoming smaller and more accessible, they are preferable in still water or without their umbilical cords to avoid becoming entangled on submerged objects. The biggest issue currently faced by ROVs is that they cannot handle strong water movement, which prevents standardised sampling protocols being followed. Both RUV and ROV, as well as the field of research in freshwater ecosystems, would benefit from method comparison studies to better understand the pros and cons and how these technologies could be used together to provide more holistic ecosystem assessments.

6 Conclusion

RUVs offer a non-destructive and effective method for monitoring freshwater fisheries species in non-turbid waters. They can provide us with very useful information to address a range of scientific questions. All future RUV surveys should consist of an action camera, set to record at 30 fps, 1080p being deployed for 60 minutes. By having a consistent methodology all future surveys can be accurately compared. These standards that we have recommended will ensure that RUV becomes a vital tool in the future of freshwater surveys. Rapid technological advances have the potential to vastly transform fisheries research to become streamlined, automated, and standardised which will improve both the quality and granularity of data that environmental managers have access to. This can greatly advance the robustness of management plans and capacity for evidence-based interventions. With the declining state of global freshwater fisheries and lack of management incentive we promote the creation of an international freshwater RUV consortium to increase standardisation, collaboration and method development to improve data availability and implement baseline monitoring programmes (Barbarossa et al., 2021; Ainsworth et al., 2023).

Acknowledgements

MH acknowledges support from the John Henry Garner Scholarship and APEM. JS and AB acknowledges support from the South African Institute for Aquatic Biodiversity and funding from UKRI Future Leaders Fellowship [Grant/Award Number: MR/X035662/1]. JS and AMD acknowledge support Water@Leeds. CJB acknowledges support from the National Research Foundation of South Africa.

Supplementary Material

Appendices A. RUV Abundance Studies.

Appendices B. RUV Species Richness Studies.

Appendices C. RUV Spawning/Mating Studies.

Appendices D. RUV Behaviour Studies.

Appendices E. RUV Migration Studies.

Appendices F. RUV Foraging Studies.

Appendices G. RUV Size Studies.

Appendices H. RUV Habitat Use Studies.

Appendices I. RUV Presence Studies.

Appendices J. RUV Nesting Studies.

Access here

References

  • Abangan AS, Kopp D, Faillettaz R. 2023. Artificial intelligence for fish behavior recognition may unlock fishing gear selectivity. Front Mar Sci 2023: 10. [Google Scholar]
  • Ainsworth RF, Cowx IG, Funge-Smith SJ. 2023. Putting the fish into inland fisheries – a global allocation of historic inland fish catch. Fish Fish 24: 263–278. [CrossRef] [Google Scholar]
  • Almero VJD, Palconit MGB, Alejandrino JD, Concepcion RS, Vicerra RRP, Sybingco E, Bandala AA, Dadios EP. 2021. Development of a raspberry Pi-based underwater camera system for inland freshwater aquaculture, in 2021 IEEE 13th International Conference on Humanoid, Nanotechnology, Information Technology, Communication and Control, Environment, and Management (HNICEM), 2021, pp. 1–6. [Google Scholar]
  • Andres KJ, Sethi SA, Duskey E, Lepak JM, Rice AN, Estabrook BJ, Fitzpatrick KB, George E, Marcy-Quay B, Paufve MR, Perkins K, Scofield AE. 2020. Seasonal habitat use indicates that depth may mediate the potential for invasive round goby impacts in inland lakes. Freshw Biol. 65: 1337–1347. [Google Scholar]
  • Bajaba SZ, Hugo S, van Wyk AJ, Marr SM, Vine NG, Weyl OLF. 2021. Can bait improve the efficiency of underwater video monitoring of fish in headwater streams? A case study from the Rondegat River, South Africa, Afr J Aquat Sci 46: 246–249. [Google Scholar]
  • Banda M, Kanyerere G, Rusuwa B. 2005. The status of the chambo in Malawi: fisheries and biology, in The Chambo Restoration Strategic Plan. WorldFish Center Conference Proceedings Vol. 71, 112 p. [Google Scholar]
  • Barbarossa V, Bosmans J, Wanders N, King H, Bierkens MFP, Huijbregts MAJ, Schipper AM. 2021. Threats of global warming to the world's freshwater fishes. Nat Commun 12: 1701. [CrossRef] [PubMed] [Google Scholar]
  • Beng KC, Corlett RT. 2020. Applications of environmental DNA (eDNA) in ecology and conservation: opportunities, challenges and prospects. Biodivers Conserv 29: 2089–2121. [CrossRef] [Google Scholar]
  • Bergman DA, Moore PA. 2003 Field observations of intraspecific agonistic behavior of two crayfish species, orconectes rusticus and orconectes virilis, in different habitats. Biol Bull 205: 26–35. [Google Scholar]
  • Block BA. 2005. Physiological ecology in the 21st century: advancements in biologging science. Integr Comp Biol 45: 305–320. [Google Scholar]
  • Boavida I, Costa MJ, Portela MM, Godinho F, Tuhtan J, Pinheiro A. 2021. Do cyprinid fish use lateral flow-refuges during hydropeaking? River Res Appl 39: 554-560. [Google Scholar]
  • Borgstrøm R, Opdahl J, Svenning MA, Länsman M, Orell P, Niemelä E, Erkinaro J, Dempson JB. 2010. Temporal changes in ascendance and in-season exploitation of Atlantic salmon, Salmo salar, inferred by a video camera array. Fish Manag Ecol 17: 454–463. [Google Scholar]
  • Boussarie G, Teichert N, Lagarde R, Ponton D. 2016. BichiCAM, an underwater automated video tracking system for the study of migratory dynamics of benthic diadromous species in streams. River Res Applic 32: 1392–1401. [Google Scholar]
  • Broom CJ, Weyl OLF, South J. 2022. Habitat associations of imperilled fishes after conservation intervention in the Cape Fold Ecoregion, South Africa. J Fish Biol 1: 1–11. [Google Scholar]
  • Broom CJ, Weyl OLF, South J. 2023. Fish community, stressors and conservation in the Rondegat River (Olifants-Doring system, Western Cape, South Africa). Fishes Mediterranean Environ 2023.001: 21. [Google Scholar]
  • Bürgi K, Bouveyron C, Lingrand D, Derijard B, Precioso F, Sabourault C. 2025. Towards a fully automated underwater census for fish assemblages in the Mediterranean Sea. Ecol Inform 85: 102959. [Google Scholar]
  • Camacho AM, Perotto-Baldivieso HL, Tanner EP, Montemayor AL, Gless WA, Exum J, Yamashita TJ, Foley AM, DeYoung RW, Nelson SD. 2023. The broad scale impact of climate change on planning aerial wildlife surveys with drone-based thermal cameras. Sci Rep 13: 4455. [Google Scholar]
  • Cappo M, Harvey ES, Shortis MR. 2006. Counting and measuring fish with baited video techniques-an overview, in AFSB Conference and Workshop Cutting-Edge Technologies in Fish and Fisheries Science. 1. [Google Scholar]
  • Caravaggi A, Banks PB, Burton AC, Finlay CMV, Haswell PM, Hayward MW, Rowcliffe MJ, Wood MD. 2017. A review of camera trapping for conservation behaviour research. Remote Sens Ecol Conserv 3: 109–122. [Google Scholar]
  • Castañeda RA, Mandrak NE, Barrow S, Weyl OLF. 2020. Occupancy dynamics of rare cyprinids after invasive fish eradication. Aquat Conserv: March Freshw Ecosyst 30: 1424–1436. [Google Scholar]
  • Cerato S, Davis AR, Coleman D, Wong MLY. 2019. Reversal of competitive dominance between invasive and native freshwater crayfish species under near-future elevated water temperature. 178. Aquat Invasions 14: 518–530. [Google Scholar]
  • Chaudoin AL, Feuerbacher OG, Bonar SA, Barrett PJ. 2015. Underwater videography outperforms above-water videography and in-person surveys for monitoring the spawning of devils hole pupfish. North Am J Fish Manag 35: 1252–1262. [Google Scholar]
  • Cooke SJ, Schreer JF. 2002. Determination of fish community composition in the untempered regions of a thermal effluent canal – the efficacy of a fixed underwater videography system. Environ Monit Assess 73: 109–129. [Google Scholar]
  • Cooke SJ, Schramm HL. 2007. Catch-and-release science and its application to conservation and management of recreational fisheries. Fish Manag Ecol 14: 73–79. [CrossRef] [Google Scholar]
  • Crook D, Wedd D, Adair B, King A, Mooney T, Harford A, Humphrey C. 2021. Fish migration in Magela Creek and potential impacts of mining-related solutes. Darwin, Australia: Charles Darwin University, ISBN 8-1-922684-14-1. [Google Scholar]
  • Dadios EP, Almero VDJ, Concepcion II R, Vicerra RRP, Bandala AA, Sybingco E. 2022. Low-cost underwater camera: design and development. J Adv Comput Intell Intell Inform 26: 851–858. [Google Scholar]
  • Delisle ZJ, Flaherty EA, Nobbe MR, Wzientek CM, Swihart RK. 2021. Next-generation camera trapping: systematic review of historic trends suggests keys to expanded research applications in ecology and conservation. Front Ecol Evol 9: 2021. [Google Scholar]
  • de Visser C, Johansson LF, Kulkarni P, Mei H, Neerincx P, van der Velde KJ, Horvatovich P, van Gool AJ, Swertz MA, Hoen PAC, Niehues A. 2023. Ten quick tips for building FAIR workflows. PLOS Comput Biol 19(9): e1011369. [Google Scholar]
  • Ditria EM, Sievers M, Lopez-Marcano S, Jinks EL, Connolly RM. 2020. Deep learning for automated analysis of fish abundance: the benefits of training across multiple habitats. Environ Monit Assess 192: 698. [Google Scholar]
  • Dunkley K, Dunkley A, Drewnicki J, Keith I, Herbert-Read JE. 2023. A low-cost, long-running, open-source stereo camera for tracking aquatic species and their behaviours. Methods Ecol Evol 14: 2549–2556. [Google Scholar]
  • Ebner BC, Fulton CJ, Cousins S, Donaldson J, Kennard MJ, Meynecke J, Schaffer J. 2015. Filming and snorkelling as visual techniques to survey fauna in difficult to access tropical rainforest streams. Mar Freshw Res 66: 120–126. [Google Scholar]
  • Ebner BC, Donaldson J, Allen GR, Keith P. 2017. Visual census, photographic records and the trial of a video network provide first evidence of the elusive Sicyopterus cynocephalus in Australia. Cybium 41: 117–125. [Google Scholar]
  • Ellender BR, Wasserman RJ, Chakona A, Skelton PH, Weyl OLF. 2017. A review of the biology and status of Cape Fold Ecoregion freshwater fishes. Aquat Conserv Mar Freshw Ecosyst 27(4): 867–879. [Google Scholar]
  • Fernández MV, Macchi PJ, Sosnovsky A, Zattara EE, Lallement ME, Milano D. 2021. Spawning aggregation behaviour in the Creole perch, Percichthys trucha (Percichthyidae): a target species for conservation. Aquat Conserv: Mar Freshw Ecosyst 31(11): 3248–3260. [Google Scholar]
  • Fetterplace LC, Ljungberg P, Benavente Norrman E, Bohlin F, Sörman L, Johannesson P, Rooth D, Königson S. 2023. AquaticVID: a low cost, extended battery life, plug-and-go video system for aquatic research. Res Ideas Outcomes 9: e114134. [Google Scholar]
  • Feyrer F, Portz D, Odum D, Newman KB, Sommer T, Contreras D, Baxter R, Slater SB, Sereno D, Nieuwenhuyse EV. 2013. SmeltCam: underwater video codend for trawled nets with an application to the distribution of the imperiled delta smelt. PLoS ONE 8(7): e67829. [Google Scholar]
  • Fleissner ER, Putland RL, Mensinger AF. 2022. The effect of boat sound on freshwater fish behavior in public (motorized) and wilderness (nonmotorized) lakes. Environ Biol Fish 105: 1065–1079. [Google Scholar]
  • Friard O, Gamba M. 2016. BORIS: a free, versatile open-source event-logging software for video/audio coding and live observations. Methods Ecol Evol 7: 1325–1330. [CrossRef] [Google Scholar]
  • Friesen RG, Chivers DP. 2006. Underwater video reveals strong avoidance of chemical alarm cues by prey fishes. Ethology 112: 339–345. [Google Scholar]
  • Glassman DM, Chhor A, Vermaire JC, Bennett JR, Cooke SJ. 2022. Does bait type and bait container configuration influence the performance of remote underwater video systems in temperate freshwater lakes for assessing fish community structure? Hydrobiologia 849: 1981–1994. [Google Scholar]
  • Groves PA, Chandler JA. 1999. Spawning habitat used by fall chinook salmon in the Snake River. North Am J Fish Manag 19: 912–922. [Google Scholar]
  • Halafo JS, Hecky RE, Taylor WD. 2004. The artisanal fishery of Metangula, Lake Malawi/Niassa, East Africa. Afr J Aquat Sci 29: 83–90. [Google Scholar]
  • Hannweg B, Marr SM, Bloy LE, Weyl OLF. 2020a. Habitat utilisation of Pseudobarbus afer and Sandelia capensis in headwaters of the Swartkops River, Eastern Cape, South Africa. Afr J Aquat Sci 45: 364–371. [Google Scholar]
  • Hannweg B, Marr SM, Bloy LE, Weyl OLF. 2020b. Using action cameras to estimate the abundance and habitat use of threatened fish in clear headwater streams. Afr J Aquat Sci 45: 372–377. [Google Scholar]
  • Hanson KC, Cooke SJ, Suski CD, Philipp DP. 2007. Effects of different angling practices on post-release behaviour of nest-guarding male black bass, Micropterus spp. Fish Manag Ecol 14: 141–148. [Google Scholar]
  • Harvey ES, McLean DL, Frusher S, Haywood MDD, Newman SJ, Williams A. 2013. The use of BRUVs as a tool for assessing marine fisheries and ecosystems: a review of the hurdles and potential. Fisheries Research and Development Corporation, and The University of Western Australia, 2012. ISBN: 978-1-74052-265-6. [Google Scholar]
  • Harwood M, Stebbing PD, Dunn AM, Cole ZK, Bradbeer SJ, Aston B, South J. 2025. Rapid assessment of population dynamics and monitoring methods for invasive narrow clawed crayfish Pontastacus leptodactylus in a freshwater reservoir. Knowl Manag Aquat Ecosyst 426: 22. [Google Scholar]
  • Haubrock PJ, Ahmed DA, Cuthbert RN, Stubbington R, Domisch S, Marquez JR, Beidas A, Amatulli G, Kiesel J, Shen LQ, Soto I, Angeler DG, Bonada N, Cañedo-Argüelles M, Csabai Z, Datry T, de Eyto E, Dohet A, Drohan E, England J, Feio MJ, Forio MAE, Goethals P, Grad W, Heino J, Hudgins EJ, Jähnig SC, Johnson RK, Larrañaga A, Leitner P, L'Hoste L, Lizee M, Maire A, Rasmussen JJ, Schäfer RB, Schmidt-Kloiber A, Vannevel R, Várbíró G, Wiberg-Larsen P, Haase P. 2022. Invasion impacts and dynamics of a European-wide introduced species. Glob Change Biol 28: 4620–4632. [Google Scholar]
  • Hawkins PR, Hortle KG, Phommanivong S, Singsua Y. 2018. Underwater video monitoring of fish passage in the Mekong River at Sadam Channel, Khone Falls, Laos. River Res Applic 34: 232–243. [Google Scholar]
  • Hitt NP, Rogers KM, Snyder CD, Dolloff CA. 2021. Comparison of underwater video with electrofishing and dive counts for stream fish abundance estimation. Trans Am Fish Soc 150: 24–37. [CrossRef] [Google Scholar]
  • Holubová M, Čech M, Vašek M, Peterka J. 2019. Density dependent attributes of fish aggregative behaviour. PeerJ 7: e6378. [Google Scholar]
  • Hopper GW. 2019. Stream flow mediates biomass, associations, and nutrient cycling of dominant animal functional groups (Unpublished doctoral thesis). USA: Kansas State University. [Google Scholar]
  • Johnson PN, Rayton MD, Nass BL, Arterburn JE. 2007. Enumeration of salmonids in the okanogan basin using underwater video, Technical Report, US Department of Energy [https://www.cbfish.org/Document.mvc/Viewer/P105814] [Google Scholar]
  • Johnson NS, Higgs D, Binder TR, Marsden JE, Buchinger T, Brege L, Bruning T, Farha S, Krueger CC. 2018. Evidence of sound production by spawning lake trout (Salvelinus namaycush) in lakes Huron and Champlain. Can J Fish Aquat Sci 75(3): 429–438. [Google Scholar]
  • Jones RE, Griffin RA, Rees SC, Unsworth RKF. 2019. Improving visual biodiversity assessments of motile fauna in turbid aquatic environments. Limnol Oceanogr Methods 17: 544–554. [Google Scholar]
  • Karatayev AY, Burlakova LE, Mehler K, Hinchey EK, Wick M, Bakowska M, Mrozinska N. 2021. Rapid assessment of Dreissena population in Lake Erie using underwater videography. Hydrobiologia 848: 2421–2436. [Google Scholar]
  • Kelaher BP, Peddemors VM, Hoade B, Colefax AP, Butcher PA. 2019. Comparison of sampling precision for nearshore marine wildlife using unmanned and manned aerial surveys. J Unmanned Veh Syst 8(1): 30–43. [Google Scholar]
  • King AJ, George A, Buckle DJ, Novak PA, Fulton CJ. 2018. Efficacy of remote underwater video cameras for monitoring tropical wetland fishes. Hydrobiologia 807: 145–164. [Google Scholar]
  • Langlois T, Goetze J, Bond T, Monk J, Abesamis RA, Asher J, Barrett N, Bernard ATF, Bouchet PJ, Birt MJ, Cappo M, Currey-Randall LM, Driessen D, Fairclough DV, Fullwood LAF, Gibbons BA, Harasti D, Heupel MR, Hicks J, Holmes TH, Huveneers C, Ierodiaconou D, Jordan A, Knott NA, Lindfield S, Malcolm HA, McLean D, Meekan M, Miller D, Mitchell PJ, Newman SJ, Radford B, Rolim FA, Saunders BJ, Stowar M, Smith ANH, Travers MJ, Wakefield CB, Whitmarsh SK, Williams J, Harvey ES. 2020. A field and video annotation guide for baited remote underwater stereo-video surveys of demersal fish assemblages. Methods Ecol Evol 11: 1401–1409. [Google Scholar]
  • Lennox RJ, Whoriskey FG, Verhelst P, Vandergoot CS, Soria M, Reubens J, Rechisky EL, Power M, Murray T, Mulder I, Markham JL, Lowerre-Barbieri SK, Lindley ST, Knott NA, Kessel ST, Iverson S, Huveneers C, Heidemeyer M, Harcourt R, Griffin LP, Friess C, Filous A, Fetterplace LC, Danylchuk AJ, Daly R, Cowley P, Cooke SJ, Chávez EJ, Blaison A, Whoriskey K. 2024. Globally coordinated acoustic aquatic animal tracking reveals unexpected, ecologically important movements across oceans, lakes and rivers. Ecography 2024: e06801. [Google Scholar]
  • Limaye S. 2019. Monitoring long island alewife populations: evaluating the efficiency of a new fishway at beaver lake in Mill Neck, NY (Unpublished masters thesis). USA: Hofstra University. [Google Scholar]
  • Lindenmayer DB, Likens GE. 2010. The science and application of ecological monitoring, Biol Conserv 143(6): 1317–1328. [Google Scholar]
  • Lindenmayer DB, Lavery T, Scheele BC. 2022. Why we need to invest in large-scale, long-term monitoring programs in landscape ecology and conservation biology. Curr Landscape Ecol Rep 7: 137–146. [Google Scholar]
  • Lintermans M, Thiem J, Broadhurst B, Ebner BC, Clear R, Starrs D, Frawley K, Norris R. 2013. Constructed homes for threatened fishes in the Cotter River catchment: Phase 1 Report, ACTEW Corporation [https://www.researchgate.net/publication/245026008_Constructed_homes_for_threatened_fishes_in_the_ Cotter_River_catchment_Phase_1_Report]. [Google Scholar]
  • Loffredo JR. 2018. Spatial and food web dynamics of non-native northern crayfish Orconectes virilis in Buffalo Lake, WA (Unpublished masters thesis). USA: Washington State University. [Google Scholar]
  • Longo GO, Hay ME, Ferreira CEL, Floeter SR. 2018 Trophic interactions across 61 degrees of latitude in the Western Atlantic. Global Ecol Biogeogr 28: 107–117. [Google Scholar]
  • Lopez LK, Hendry K, Wong MY, Davis AR. 2019. Insight into invasion: interactions between a critically endangered and invasive crayfish. Austral Ecol 44: 78–85. [Google Scholar]
  • MacNeil MA, Chapman DD, Heupel M, Simpfendorfer CA, Heithaus M, Meekan M, Harvey E, Goetze J, Kiszka J, Bond ME, Currey-Randall LM, Speed CW, Sherman CS, Rees MJ, Udyawer V, Flowers KI, Clementi G, Valentin-Albanese J, Gorham T, Adam MS, Ali K, Pina-Amargós F, Angulo-Valdés JA, Asher J, Barcia LG, Beaufort O, Benjamin C, Bernard ATF, Berumen ML, Bierwagen S, Bonnema E, Bown RMK, Bradley D, Brooks E, Brown JJ, Buddo D, Burke P, Cáceres C, Cardeñosa D, Carrier JC, Caselle JE, Charloo V, Claverie T, Clua E, Cochran JEM, Cook N, Cramp J, D'Alberto B, de Graaf M, Dornhege M, Estep A, Fanovich L, Farabaugh NF, Fernando D, Flam AL, Floros C, Fourqurean V, Garla R, Gastrich K, George L, Graham R, Guttridge T, Hardenstine RS, Heck S, Henderson AC, Hertler H, Hueter R, Johnson M, Jupiter S, Kasana D, Kessel ST, Kiilu B, Kirata T, Kuguru B, Kyne F, Langlois T, Lédée EJI, Lindfield S, Luna-Acosta A, Maggs J, Manjaji-Matsumoto BM, Marshall A, Matich P, McCombs E, McLean D, Meggs L, Moore S, Mukherji S, Murray R, Kaimuddin M, Newman SJ, Nogués J, Obota C, O'Shea O, Osuka K, Papastamatiou YP, Perera N, Peterson B, Ponzo A, Prasetyo A, Quamar LMS, Quinlan J, Ruiz-Abierno A, Sala E, Samoilys M, Schärer-Umpierre M, Schlaff A, Simpson N, Smith ANH, Sparks L, Tanna A, Torres R, Travers MJ, Bergmann MZ, Vigliola L, Ward J, Watts AM, Wen C, Whitman E, Wirsing AJ, Wothke A, Zarza-Gonzâlez E, Cinner JE. 2020. Global status and conservation potential of reef sharks. Nature 583: 801–806. [Google Scholar]
  • Magneville C, Leréec Le Bricquir ML, Dailianis T, Skouradakis G, Claverie T, Villéger S. 2023. Long-duration remote underwater videos reveal that grazing by fishes is highly variable through time and dominated by non-indigenous species. Remote Sens Ecol Conserv 9: 311–322. [Google Scholar]
  • Magneville C, Brissaud C, Fleuré V, Loiseau N, Claverie T, Villéger S. 2024. A new framework for estimating abundance of animals using a network of cameras. Limnol Oceanogr Methods 22: 268–280. [Google Scholar]
  • Mallet D, Pelletier D. 2014. Underwater video techniques for observing coastal marine biodiversity: a review of sixty years of publications (1952–2012). Fish Res 154: 44–62. [Google Scholar]
  • Marchand F, Magnan P, Boisclair D. 2002. Water temperature, light intensity and zooplankton density and the feeding activity of juvenile brook charr (Salvelinus fontinalis). Freshw Biol 47: 2153–2162. [Google Scholar]
  • Marr SM, Impson ND, Tweddle D. 2012. An assessment of a proposal to eradicate non-native fish from priority rivers in the Cape Floristic Region, South Africa. Afr J Aquat Sci 37(2): 131–142. [Google Scholar]
  • Marston BR. 2014. Situk River Steelhead Stock Assessment, 2014-2015, Regional Operational Plan SF.1J.2014.09, Alaska Department of Fish and Game, Division of Sport Fish, Yakutat [https://www.adfg.alaska.gov/FedAidPDFs/ROP.SF.1J.2014.09.pdf] [Google Scholar]
  • Martin AL, Moore PA. 2007. Field observations of agonism in the crayfish, Orconectes rusticus: shelter use in a natural environment. Ethology 113: 1192–1201. [Google Scholar]
  • Martin B, Irwin ER. 2010. A digital underwater video camera system for aquatic research in regulated rivers. North Am J Fish Manag 30: 1365–1369. [Google Scholar]
  • Mena-Valenzuela P, Valdiviezo-Rivera J, Mena-Olmedo J, Aguirre WE. 2022. The first observation of copulation in Andean catfish Astroblepus ubidiai (Siluriformes, Astroblepidae), in Lago San Pablo, Imbabura, Ecuador. J Fish Biol. 101(5): 1348–1352. [Google Scholar]
  • Moore A, Scott A. 1988. Observations of recently emerged sea trout, Salmo trutta L., fry in a chalk stream, using a low-light underwater camera. J Fish Biol 33: 959–960. [Google Scholar]
  • Morán-López R, Uceda-Tolosa O. 2017. Image techniques in turbid rivers: A ten-year assessment of cyprinid stocks composition and size. Fish Res 195: 186–193. [Google Scholar]
  • Morán-López R, Uceda-Tolosa O. 2020. Biomechanics of fish swimming and leaping under waterfalls: a realistic field, image-based biophysical model with bioengineering implications. Bioinspir Biomim 15. https://doi.org/10.1088/1748-3190/ab9b64. [Google Scholar]
  • Moran CJ, Rzucidlo CL, Ellerby DJ, Gerry SP. 2019. Laboratory constraints on feeding behaviours in polymorphic bluegill sunfish (Lepomis macrochirus). Freshw Biol 64: 926–932. [Google Scholar]
  • Musslewhite JG. 2020. Neva Lake Sockeye Salmon Stock Assessment, 2019, Annual Report for Study 18-607, U.S. Fish and Wildlife Service, Office of Subsistence Management, Fisheries Resource Monitoring Program [https://www.hia-env.org/wp-content/uploads/2020/12/Neva-18-607-2019-annual-report-002.pdf]. [Google Scholar]
  • Negrea C, Thompson DE, Juhnke SD, Fryer DS, Loge FJ. 2014. Automated detection and tracking of adult pacific lampreys in underwater video collected at Snake and Columbia River Fishways. North Am J Fish Manag 34. (1): 111-118. [Google Scholar]
  • O'Hea Miller SB, Davis AR, Wong MYL. 2022a. Further insights into invasion: field observations of behavioural interactions between an invasive and critically endangered freshwater crayfish using Baited Remote Underwater Video (BRUV). Biology 12: 18. [Google Scholar]
  • O'Hea Miller SB, Davis AR, Wong MYL. 2022b. Does habitat complexity and prior residency influence aggression between invasive and native freshwater crayfish? Ethology 128: 443–452. [Google Scholar]
  • O'Malley BP, Dillon RA, Paddock RW, Hansson S, Stockwell JD. 2018. An underwater video system to assess abundance and behavior of epibenthic Mysis. Limnol Oceanogr: Methods 16(12): 868-880. [Google Scholar]
  • Ovalle JC, Vilas C, Antelo LT. 2022. On the use of deep learning for fish species recognition and quantification on board fishing vessels. Mar Policy 139: 105015. [Google Scholar]
  • Page MJ, McKenzie JE, Bossuyt PM, Boutron I, Hoffmann TC, Mulrow CD, Shamseer L, Tetzlaff JM, Akl EA, Brennan SE, Chou R, Glanville J, Grimshaw JM, Hróbjartsson A, Lalu MM, Li T, Loder EW, Mayo-Wilson E, McDonald S, McGuinness LA, Stewart LA, Thomas J, Tricco AC, Welch VA, Whiting P, Moher D. 2021a. The PRISMA 2020 statement: an updated guideline for reporting systematic reviews. BMJ 372: n71. [Google Scholar]
  • Page MJ, Moher D, Bossuyt PM, Boutron I, Hoffmann TC, Mulrow CD, Shamseer L, Tetzlaff JM, Akl EA, Brennan SE, Chou R, Glanville J, Grimshaw JM, Hróbjartsson A, Lalu MM, Li T, Loder EW, Mayo-Wilson E, McDonald S, McGuinness LA, Stewart LA, Thomas J, Tricco AC, Welch VA, Whiting P, McKenzie JE. 2021b. PRISMA 2020 explanation and elaboration: updated guidance and exemplars for reporting systematic reviews. BMJ 372: n160. [Google Scholar]
  • Pedersen SLK. 2021. Evaluation and use of a monitoring method to estimate Atlantic salmon spawning run, (Unpublished masters thesis). Norway: The Arctic University of Norway. [Google Scholar]
  • Phillips B, Shipley ON, Halvorsen J, Sternlicht JK, Gallagher AJ. 2019. First in situ observations of the sharpnose sevengill shark (Heptranchias perlo), from the Tongue of the Ocean, Bahamas. J Ocean Sci Found 32: 17–22. [Google Scholar]
  • Pledger AG, Rice SP, Millett J. 2014. Reduced bed material stability and increased bedload transport caused by foraging fish: a flume study with juvenile Barbel (Barbus barbus). Earth Surf Process Landforms 39: 1500–1513. [Google Scholar]
  • Pratt TE, Smokorowski KE, Muirhead JR. 2005. Development and experimental assessment of an underwater video technique for assessing fish-habitat relationships. Archiv für Hydrobiologie 164: 547–571. [Google Scholar]
  • Raugstad T. 2019. Using underwater filming to study activity and fighting behavior in Astacus astacus (Unpublished masters thesis). Norway: Universitetet I Oslo. [Google Scholar]
  • Robinson KM, Galarowicz TL, O'Neill P, Chadderton WL, Claramunt RM, Herbert M, Tucker AJ. 2019. Monitoring shallow benthic fish assemblages in the Laurentian Great Lakes using baited photoquadrats: enhancing traditional fisheries monitoring methods. J Great Lakes Res 45(2): 333-339. [Google Scholar]
  • Satoh S, Saeki T, Kohda M, Awata S. 2022. Cooperative breeding in Neolamprologus bifasciatus, a cichlid fish inhabiting the deep reefs of Lake Tanganyika. Ecol Freshw Fish 31: 640–649. [Google Scholar]
  • Shortis MR, Otis T. 2014. Progress toward automation of salmon escapement counts. CEUR Workshop Proc 1307. https://hdl.handle.net/10779/rmit.27391260. [Google Scholar]
  • Skorulis A, Wong M, Davis A. 2021. Assessing trap bias in the endemic Australian genus of freshwater crayfish, Euastacus. Mar Freshw Res 73(1): 100-109. [Google Scholar]
  • Šmejkal M, Baran R, Blabolil P, Vejřík L, Prchalová M, Bartoň D, Mrkvička T, Kubečka J. 2017. Early life-history predator-prey reversal in two cyprinid fishes. Sci Rep 7: 6924. [Google Scholar]
  • Smith A. 2022. Seasonal microhabitat preference for minnows in low order streams, (Unpublished masters thesis). Canada: The University of Guelph. [Google Scholar]
  • Soom J, Pattanaik V, Leier M, Tuhtan JA. 2022. Environmentally adaptive fish or no-fish classification for river video fish counters using high-performance desktop and embedded hardware. Ecol Inform 72: 101817. [Google Scholar]
  • Spears BM, Gunn IDM, Carvalho L, Winfield IJ, Dudley B, Murphy K, May L. 2009. An evaluation of methods for sampling macrophyte maximum colonisation depth in Loch Leven, Scotland. Aquat Botany 91(2): 75–81. [Google Scholar]
  • Starrs D, Ebner BC, Fulton CJ. 2015. Ceasefire: minimal aggression among Murray River crayfish feeding upon patches of allochthonous material. Aust J Zool 63(2): 115–121. [Google Scholar]
  • Struthers DP, Danylchuk AJ, Wilson ADM, Cooke SJ. 2015. Action cameras: bringing aquatic and fisheries research into view. Fisheries 40: 502–512. [Google Scholar]
  • Sundin J, Morgan R, Finnøen MH, Dey A, Sarkar K, Jutfelt F. 2019. On the observation of wild zebrafish (Danio rerio) in India. Zebrafish 16(6): 546–553. [Google Scholar]
  • Svenning MA, Lamberg A, Dempson B, Strand R, Hanssen ØK, Fauchald P. 2017. Incidence and timing of wild and escaped farmed Atlantic salmon (Salmo salar) in Norwegian rivers inferred from video surveillance monitoring. Ecol Freshw Fish 26: 360–370. [Google Scholar]
  • Tickner D, Opperman JJ, Abell R, Acreman M, Arthington AH, Bunn SE, Cooke SJ, Dalton J, Darwall W, Edwards G, Harrison I, Hughes K, Jones T, Leclère D, Lynch AJ, Leonard P, McClain ME, Muruven D, Olden JD, Ormerod SJ, Robinson J, Tharme RE, Thieme M, Tockner K, Wright M, Young L. 2020. Bending the curve of global freshwater biodiversity loss: an emergency recovery plan. BioScience 70(4): 330–342. [CrossRef] [PubMed] [Google Scholar]
  • Tweddle D, Magasa J. 1989. Assessment of multispecies cichlid fisheries of the Southeast Arm of Lake Malawi, Africa. ICES J Mar Sci 45: 209–222. [Google Scholar]
  • Tweedie J, Cockburn J, Villard P. 2018. Bioenergetics models as a means to evaluate channel habitat availability [powerpoint slides]. Canada: Department of Geography, University of Guelph. [http://www.allsetinc.com/website_nc/files/presentations_2018/NC2018_T3C_John_Tweedie_Jaclyn_Cockburn.pdf]. [Google Scholar]
  • Unger S, Hickman C. 2019. Report on the short-term scavenging of decomposing native and non-native trout in appalachian streams. Fishes 4: 17. [Google Scholar]
  • Unger S, Jachowski CMB, Diaz L, Williams LA. 2020. Shelter Guarding Behavior of the Eastern Hellbender (Cryptobranchus alleganiensis alleganiensis) in North Carolina Streams. Southeast Nat 19(4): 742–758. [Google Scholar]
  • Usvyatsov S, Watmough J, Litvak MK. 2012. Age and population size estimates of overwintering shortnose sturgeon in the Saint John River, New Brunswick, Canada. Trans Am Fish Soc 141: 1126–1136. [Google Scholar]
  • van Wyk AJ, Hugo S, Ado AP, Weyl OLF. 2017. Improved Benefit Sharing and Monitoring in Lake Niassa Technical Report Final Report on September 2017 Surveys. 10.13140/RG.2.2.14060.28807. [Google Scholar]
  • van Wyk AJ. 2019. Evaluation of Baited Remote Underwater Video Systems (BRUVS) for monitoring fish communities in Lake Malawi/Niassa (Unpublished masters thesis). South Africa: Rhodes University. [Google Scholar]
  • Weyl OLF. 2005. Capture fisheries in Malawi and their contribution to national fish supply. Aquaculture Development in Malawi (ADiM) report. Grahamstown, South Africa: Enviro-Fish Africa (Pty) Ltd.. [Google Scholar]
  • Weyl OLF, Ribbink AJ, Tweddle D. 2010. Lake Malawi: fishes, fisheries, biodiversity, health and habitat. Aquat Ecosyst Health Manag 13: 241–254. [Google Scholar]
  • Weyl OLF, Ellender BR, Woodford DJ, Jordaan MS. 2013. Fish distributions in the Rondegat River, Cape Floristic Region, South Africa, and the immediate impact of rotenone treatment in an invaded reach. Afr J Aquat Sci 38: 201–209. [Google Scholar]
  • Weyl OLF, Finlayson B, Impson ND, Woodford DJ, Steinkjer J. 2014. Threatened endemic fishes in South Africa's Cape Floristic Region: a new beginning for the Rondegat River. Fisheries 39(6): 270–279. [Google Scholar]
  • Weyl OLF, Barrow S, Bellignan T, Dalu T, Ellender BR, Elser K, Impson D, Gouws J, Jordaan M, Villet M, Wasserman RJ, Woodford DJ. 2016. Monitoring of invertebrate and fish recovery following river rehabilitation using rotenone in the Rondegat River. WRC Report No. 2261/1/16, ISBN 978-1-4312-0788-6. [Google Scholar]
  • Whitmarsh SK, Fairweather PG, Huveneers C. 2017. What is Big BRUVver up to? Methods and uses of baited underwater video. Rev Fish Biol Fish 27: 53–73. [Google Scholar]
  • Widmer L, Heule E, Colombo M, Rueegg A, Indermaur A, Ronco F, Salzburger W. 2019. Point-Combination Transect (PCT): incorporation of small underwater cameras to study fish communities. Methods Ecol Evol 10: 891–901. [Google Scholar]
  • Wohlin C. 2014. Guidelines for snowballing in systematic literature studies and a replication in software engineering, in Proceedings 18th International Conference on Evaluation and Assessment in Software Engineering (EASE 2014), pp. 321–330, London, UK, May 2014. [Google Scholar]
  • Work K, Jennings CJ. 2019. Underwater video surveys provide a more complete picture of littoral fish populations than seine samples in clear Florida springs. Mar Freshw Res 70: 1178–1184. [Google Scholar]
  • Yamane H, Nagata Y, Watanabe K. 2016. Exploitation of the eggs of nest associates by the host fish Pseudobagrus nudiceps. Ichthyol Res 63: 23–30. [Google Scholar]

Cite this article as: Harwood M, Broom CJ, van Wyk A, Castañeda RA, Wong MYL, Bernard ATF, Stebbing PD, Dunn AM, South J. 2026. Application, development and opportunities of Remote Underwater Video for freshwater fisheries management . Knowl. Manag. Aquat. Ecosyst., 427, 5, https://doi.org/10.1051/kmae/2026001

All Tables

Table 1

Keyword combinations used in initial literature search.

Table 2

Prevalence of technology and methods reporting in the literature.

Table 3

Recommended standards and reasoning.

All Figures

thumbnail Fig. 1

PRISMA flow diagram illustrating the different phases of the systematic literature review data identification and inclusion.

In the text
thumbnail Fig. 2

Histogram of literature related to RUVs in freshwater released each year.

In the text

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