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Marine mammal sightings around oil and gas installations in the central North Sea

Published online by Cambridge University Press:  13 June 2017

Matthieu Delefosse*
Affiliation:
Maersk Oil, Health, Safety and Environment, Britanniavej 10, DK-6700 Esbjerg, Denmark
Malene Louise Rahbek
Affiliation:
DONG Oil & Gas, Nesa Allé 1, DK-2820 Gentofte, Denmark
Lars Roesen
Affiliation:
Hess Denmark APS, Østergade 26B, DK-1100 Copenhagen, Denmark
Karin Tubbert Clausen
Affiliation:
Department of Bioscience, Aarhus University, Frederiksborgvej 399, DK-4000 Roskilde, Denmark
*
Correspondence should be addressed to: M. Delefosse, Maersk Oil, Chemistry and Environment, Britanniavej 10, DK-6700 Esbjerg, Denmark email: matthieu.delefosse@maerskoil.com
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Abstract

Relatively little is known about the distribution and diversity of marine mammals around offshore anthropogenic structures. We present results obtained from incidental sightings of marine mammals around oil and gas installations located 200 km off the Danish coast. A total of 131 sightings corresponding to about 288 animals were reported between May 2013 and May 2016. A total of seven marine mammal species were identified, five cetaceans: harbour porpoise (Phocoena phocoena), minke whale (Balaenoptera acutorostrata), white-beaked dolphin (Lagenorhynchus albirostris), killer whale (Orcinus orca), pilot whales (Globicephala spp.) and two species of pinnipeds: harbour (Phoca vitulina) and grey seals (Halichoerus grypus). The most sighted species were harbour porpoise (41%) and minke whale (31%). Relative counts and biodiversity of marine mammals observed around installations corresponded well with the expected distribution in the central North Sea. Several taxon-specific correlations were identified between number of sightings and environmental parameters (depth and latitude) or installation characteristics (installation aerial footprint). Furthermore, 85% of sightings were made during spring and summer and it is unclear whether the pattern observed reflected a natural seasonal occurrence of marine mammals in the area or an effect of reduced effort during autumn and winter. Despite the potential caveats, results obtained during this programme provide an insight into the relationship between marine mammals and oil and gas offshore installations in the North Sea.

Type
Research Article
Creative Commons
Creative Common License - CCCreative Common License - BY
This is an Open Access article, distributed under the terms of the Creative Commons Attribution licence (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted re-use, distribution, and reproduction in any medium, provided the original work is properly cited.
Copyright
Copyright © Marine Biological Association of the United Kingdom 2017

INTRODUCTION

Marine ecological monitoring programmes have become an important tool for environmental management worldwide (Borja et al., Reference Borja, Bricker, Dauer, Demetriades, Ferreira, Forbes, Hutchings, Jia, Kenchington, Marques and Zhu2008; Borja & Elliott, Reference Borja and Elliott2013). The programmes provide managers and decision-makers with an essential source of relevant, reliable and timely science-based information that can be used to support the decision-making process (Elliott, Reference Elliott2011). The North Sea is a region with a wide range of industrial activities (OSPAR, 2010; Andersen et al., Reference Andersen, Stock, Heinänen, Mannerla and Vinther2013) and it is home for several protected marine mammal species (Kinze, Reference Kinze2001; Reid et al., Reference Reid, Evans and Northridge2003; Hammond et al., Reference Hammond, Macleod, Berggren, Borchers, Burt, Cañadas, Desportes, Donovan, Gilles, Gillespie, Gordon, Hiby, Kuklik, Leaper, Lehnert, Leopold, Lovell, Øien, Paxton, Ridoux, Rogan, Samarra, Scheidat, Sequeira, Siebert, Skov, Swift, Tasker, Teilmann, Van Canneyt and Vázquez2013). Acquisition of data on the distribution of highly migratory animals, such as marine mammals, over a wide geographic area, is challenging logistically and economically and often it requires large collaborative international efforts (Hammond et al., Reference Hammond, Macleod, Berggren, Borchers, Burt, Cañadas, Desportes, Donovan, Gilles, Gillespie, Gordon, Hiby, Kuklik, Leaper, Lehnert, Leopold, Lovell, Øien, Paxton, Ridoux, Rogan, Samarra, Scheidat, Sequeira, Siebert, Skov, Swift, Tasker, Teilmann, Van Canneyt and Vázquez2013; Koblitz et al., Reference Koblitz, Amundin, Carlström, Thomas, Carlén, Teilmann, Tregenza, Wennerberg, Kyhn, Svegaard, Koza, Kosecka, Pawliczka, Tiberi Ljungqvist, Brundiers, Wright, Mikkelsen, Tougaard, Loisa, Galatius, Jüssi and Benke2014). Alternative methods based on incidental sightings by sea-users (e.g. recreational sailors, fishermen, ferry goers) may be a cost-effective means to provide complementary valuable information to large regional surveys (Evans et al., Reference Evans, Anderwald and Baines2003; Kinze et al., Reference Kinze, Jensen and Skov2003; Loos et al., Reference Loos, Cooke, Deimer, Fietz, Henning and Schütte2009; Palacios et al., Reference Palacios, Herrera, Gerrodette, Garcia, Soler, Avila, Bessudo, Hernandez, Trujillo and Flórez-González2012).

In recent years, participation of the public community in collection of ecological survey data has greatly intensified under the concept of ‘citizen science’ (Devictor et al., Reference Devictor, Whittaker and Beltrame2010; Conrad & Hilchey, Reference Conrad and Hilchey2011). Adequately trained citizen scientists are a cost effective means to acquire valuable long-term data over a wide geographic area or access important scientific background information in new areas (Robinson et al., Reference Robinson, Jaidah, Jabado, Lee-Brooks, Nour El-Din, Malki, Elmeer, McCormick, Henderson, Pierce and Ormond2013; Embling et al., Reference Embling, Walters and Dolman2015). For example, marine mammal observations by shore-based citizen scientists have been collected for more than 40 years in the UK and the data have proven to be beneficial for coastal environmental management (Evans et al., Reference Evans, Anderwald and Baines2003, Reference Evans, Pierce, Veneruso, Weir, Gibas, Anderwald and Santos2015; Reid et al., Reference Reid, Evans and Northridge2003). Elsewhere, offshore incidental sightings have also contributed to the discovery of a major aggregation site for whale sharks in proximity to an offshore installation in the Al Shaheen area in the Arabian Gulf, 90 km off the coast of Qatar (Robinson et al., Reference Robinson, Jaidah, Jabado, Lee-Brooks, Nour El-Din, Malki, Elmeer, McCormick, Henderson, Pierce and Ormond2013).

Incidental sightings of seals, dolphins and whales around oil and gas (O&G) installations in the North Sea have also been reported by offshore staff for several decades (Evans, Reference Evans1976; Evans et al., Reference Evans, Anderwald and Baines2003), but rarely has there been sustained systematic effort (Todd et al., Reference Todd, Warley and Todd2016). To increase our knowledge on the relationship between marine mammals and the presence of O&G installations in the central Danish North Sea, an offshore marine mammal sighting reporting programme (MMSR) was initiated in May 2013. The programme was used as an incentive for staff working on and around offshore O&G installations in Denmark to report more systematically their incidental marine mammal sightings. Our objectives were (1) to collect local information on marine mammal occurrence and biodiversity around offshore O&G installations in the central Danish North Sea, and (2) to obtain a general picture of the regional distribution of marine mammals across an O&G activity region. Here, we present incidental sightings data collected during the first 3 years of the MMSR programme.

METHODS

Study site

Currently, there are about 25 fixed oil and gas installations in the Danish part of the central North Sea (Figure 1). Some of these installations are manned continuously by crew, while ‘satellite’ installations are visited occasionally by a small crew for a few hours. All installations are located around 200 km from the west coast of Denmark. In the north, installations are more recent with smaller submerged structures, and smaller permanent crew compared with the southern installations. Northern installations operate at depths ranging between 55 and 66 m, whereas southern installations operate at shallower depths ranging from 33 to 46 m (Table 1). Supply-, survey- and standby-boats, accommodation and drilling rigs are often placed or operate close to installations (within 750 m from the installations) increasing the size of crew associated with a specific installation for a period, which may range from hours to several weeks.

Fig. 1. Study area. Filled symbols show continuously manned installations and open symbols show satellite installations which are occasionally visited. Installation group names are indicated in Table 1.

Table 1. Danish installations overview in 2016. Construction date refers to construction of the first element of an installation which may have been expanded incrementally over the years. Areal footprint corresponds to cumulative area covered by the platform's legs at the seafloor and was estimated based on high resolution schematic drawing of the installations.

Regional marine mammal surveys indicate that the most common cetaceans in the Danish central North Sea are harbour porpoise (Phocoena phocoena; 0.293 individuals km−2), white-beaked dolphin (Lagenorhynchus albirostris 0.047 individuals km−2), and minke whale (Balaenoptera acutorostrata; 0.028 individuals km−2; Hammond et al., Reference Hammond, Macleod, Berggren, Borchers, Burt, Cañadas, Desportes, Donovan, Gilles, Gillespie, Gordon, Hiby, Kuklik, Leaper, Lehnert, Leopold, Lovell, Øien, Paxton, Ridoux, Rogan, Samarra, Scheidat, Sequeira, Siebert, Skov, Swift, Tasker, Teilmann, Van Canneyt and Vázquez2013). Other marine mammal species are also known to occur in the area in lesser numbers: grey and harbour seals (Halichoerus grypus; Phoca vitulina), sperm whale (Physeter macrocephalus), fin whale (Balaenoptera physalus) and several species of dolphins including killer whale (Orcinus orca) and pilot whales (Globicephala spp.), as well as Atlantic white-sided (Lagenorhynchus acutus), bottlenose (Tursiops truncatus), common (Delphinus delphis) and striped dolphins (Stenella coeruleoalba) (Kinze, Reference Kinze2001; Evans et al., Reference Evans, Anderwald and Baines2003; Reid et al., Reference Reid, Evans and Northridge2003; Hammond et al., Reference Hammond, Macleod, Berggren, Borchers, Burt, Cañadas, Desportes, Donovan, Gilles, Gillespie, Gordon, Hiby, Kuklik, Leaper, Lehnert, Leopold, Lovell, Øien, Paxton, Ridoux, Rogan, Samarra, Scheidat, Sequeira, Siebert, Skov, Swift, Tasker, Teilmann, Van Canneyt and Vázquez2013).

Reporting system

Commencement of the Danish offshore marine mammal sighting reporting programme (MMSR) was communicated to offshore platform workers and contractors through different media: presentations, emails, information meetings, intranet, an internally distributed magazine, and posters displayed offshore. Status updates and reminders about the MMSR were sent monthly the first year and quarterly thereafter, via the same channels, to maintain as high a level of involvement of the volunteers as possible (Loos et al., Reference Loos, Cooke, Deimer, Fietz, Henning and Schütte2009). Charts and identification keys to assist recognition of the most common species expected in the central North Sea were prepared by marine mammal biologists (modified from Jefferson et al., Reference Jefferson, Webber and Pitman2011 and http://www.hvaler.dk). The material was posted offshore on crew information boards and also made available in electronic format at the commencement of MMSR on 1 May 2013 and at each of the status updates and reminders.

Observations were made with the naked eye at an elevation of 25–70 m above sea level when stationed on installations or rigs and a maximum elevation of 15 m above sea level when stationed on boats. Volunteers reporting their incidental sightings were requested to report as a minimum: location, date and time of sighting, number of individuals (adult/calf) and behaviour. Individuals were identified to species level, though this was not always possible for dolphins (e.g. Lagenorhynchus albirostris or L. acutus) or seals, as differentiation can be difficult under typical offshore sighting conditions (Jefferson et al., Reference Jefferson, Webber and Pitman2011). Some reports included a visual estimate of distance from installation to the marine mammal, an estimate of size of the animal and description of its colouration pattern. When several sightings of the same species were made by different reporters at the same time, day and from the same installation, only the sighting with the greatest number of individuals was used for further data analysis. Reports were usually provided by email within 24 h of sighting. Photographs and videos were provided when available, and marine mammal biologists made a posteriori identification of documented reports.

Weather conditions

Sightability of marine mammals generally depends on sea state and weather conditions (Clarke, Reference Clarke1982). For example harbour porpoises, the smallest and most common species expected in the area, can only be observed reliably at Beaufort sea states ≤2 (Teilmann, Reference Teilmann2003). As reports were not provided with a sea state description, wind data collected on the platform were converted to the Beaufort scale. Empirical wind speed measurements were taken by wind gauges installed on the different installations. The measurements were not always available at some locations and the wind dataset collected at Tyra West was selected as a proxy for the wind conditions at all installations over the duration of the programme. This dataset was the most complete and correlated best with wind measurements collected at other installations (r = 0.78–0.93; P < 0.001). Average wind data were recorded as a 10-min window every hour. The measurements were taken in metres per second (m s−1) at 30 m above sea level and back-calculated to a 10 m elevation using the formula: v (m s−1; @10 m) = 0.876 v (m s−1 @ 30 m). Wind data were converted to the Beaufort scale by the formula B = 1.20 v2/3, where v is the wind speed in m s−1 at a 10 m elevation and B is rounded to obtain the Beaufort scale number (Beer, Reference Beer1996). As sightings are not possible at night, only median wind speeds for daylight hours were used. Daylight start, end and duration were estimated using civilian day for the central North Sea (Todd et al., Reference Todd, Pearse, Tregenza, Lepper and Todd2009).

Data analysis

The data included in the analyses are from sightings made during the three first years of MMSR, corresponding to the period from 1 May 2013 to 1 May 2016.

The total number of sightings for the different seasons was compared by a Kruskal–Wallis test (ANOVA by rank). Seasons were defined as winter (January–March), spring (April–June), summer (July–September) and autumn (October–December). Spearman's rank order correlations were estimated between total number of sightings and wind speed, as well as between total number of sightings and number of daylight hours at Beaufort ≤2.

Furthermore, Spearman's rank order correlations were estimated between species-specific numbers of sightings and environmental parameters (depth, longitude and latitude ED50, UTM zone 31) or installation characteristics (construction year and aerial footprint; Table 1). Due to low numbers of sightings for some of the individual installations, sighting data were aggregated based on their proximity, in three installation groups (HARALD, SIRI, S. ARNE) in the northern area and four groups (DAN, GORM, HALFDAN and TYRA) in the southern area (Table 1 and Figure 1). Group of installations with larger crew have a higher number of potential volunteer reporters i.e. a proxy for observation effort; thus the Spearman correlations parameters (r- and ρ-values) were estimated on the sighting data that were corrected by calculating the ratio between raw sighting numbers and installation group crew size. Some species had a limited number of observations, preventing reliable specific data analysis. In such cases, sightings data analyses were done based on higher taxonomic level sighting data e.g. Delphinidae (dolphins) or Phocidae (seals).

Kruskal–Wallis's and Spearman's statistical parameter for each of the tests were estimated using STATISTICA v.12.

RESULTS

General results

A total of 131 marine mammal incidental sightings corresponding to about 288 individuals were reported during the three years of the marine mammal sighting reporting programme (MMSR; 1 May 2013 to 1 May 2016; Table 2). The most sighted species around the Danish oil and gas installations were harbour porpoise (41%) and minke whale (31%). Other marine mammals sighted included at least three species of dolphins (11%) – killer whale, pilot whale and white-beaked dolphin, and two species of seals (15%) – harbour and grey seals. Harbour porpoise calves were observed in 50% of the porpoise sightings from May to September, and dolphin calves were observed twice in July. About 20% of reports were documented either by photographs or videos (Figure 2; online Supplementary file), and marine mammal biologists confirmed that species identification in 26 out of the 28 documented reports was reported correctly by offshore staff.

Fig. 2. Minke whale photographed at Halfdan A in June 2014. Note the presence of a drilling rig and a supply boat. Credit: Henrik Ærenlund Olsen (Esvagt Promotor).

Table 2. Summary of reported sightings from the Danish oil and gas activity area from 1 May 2013 to 1 May 2016. The summary is based on species/taxa and group size.

Marine mammals were most frequently observed solitarily or in groups of two individuals (Table 2). Sightings of pods of more than five individuals were relatively rare (3%) and only reported for minke whales and dolphin species. Marine mammal sightings were most often reported from offshore fixed installations (65%) and nearby standby boats (31%). Animals were observed swimming under installation legs out to a distance of several hundred metres. On several occasions, seals were observed resting intermittently on the lower structures of the installations for several days, and in one instance, pictures showed a young grey seal on the deck of the smallest standby-boat.

Interestingly, sightings of some fish species were also reported as part of the MMSR. A 0.5 m wide sunfish (Mola mola) was seen at Valdemar in June 2014, and another was photographed at Halfdan B in July 2015. An ~10 m long basking shark (Cetorhinus maximus) was reported and video recorded feeding around the Tyra East installation in October 2015 (https://youtu.be/H93WTZp4xv8).

Temporal and spatial variability

There were significant seasonal differences between the numbers of marine mammal sightings (Kruskal–Wallis; N = 12; P = 0.053). The majority of reported sightings were made during spring (40%) and summer (48%), whereas only three sightings (2%) were made during autumn. The highest number of sightings was made in July with a total of 37 (Figure 3). Daylight hours available ranged from a monthly average of 286 h for autumn and winter to 467 h for spring and summer. Additionally, Beaufort wind force ≤2 corresponded to an estimated 11% of the daytime in spring, 17% in summer, 5% in autumn and 8% in winter. July had the highest number of daytime hours with about 545 h and an estimated 39% of the daytime with Beaufort wind force ≤2. The overall number of monthly sightings decreased with increasing wind speed (Spearman ρ < 0.001; r 2 = 0.79) and with decreasing daytime hours with Beaufort wind force ≤2 (Spearman ρ < 0.001; r 2 = 0.73). The total number of daytime hours with Beaufort wind force ≤2 was 667 in the first year (1 May 2013 to 1 May 2014), 461 h in the second year and 460 h in the third year. The number of reported marine mammal sightings was 33 during the first monitoring year, 58 during the second year, and 40 during the third year.

Fig. 3. Monthly marine mammal sighting counts (top) and corresponding wind speed and daylight hours (bottom). Box plots indicate civilian daylight hours median wind speed (line), 25 and 75% (lower and upper box sides) and 5 and 95% over the duration of the reporting programme (lower and upper whiskers) limits (N = 693–1698).

Ninety-three per cent of sightings were made around southern installations, particularly at HALFDAN (40%; Figure 4). Sightings from southern installations were mostly of harbour porpoise (50%) and minke whale (33%), but dolphins (13%) and seals (5%) were also observed. At northern installations, sightings were mostly of minke whale (75%) and one single report of four harbour porpoises. There were significant taxon specific correlations between sighting numbers and some of the environmental characteristics (latitude and depth) and installations characteristics (aerial installation footprint; Table 3). This relationship was particularly strong for harbour porpoise, with an increase in the number of sightings from north to south (Spearman ρ = 0.003; r 2 = 0.85). There was also an increase in number of harbour porpoise sightings with aerial installation footprint (Spearman ρ = 0.033; r 2 = 0.62). The number of sightings increased with increasing depth for seals (Spearman ρ = 0.023; r 2 = 0.67) and dolphins (Spearman ρ = 0.007; r 2 = 0.79).

Fig. 4. Marine mammal sightings counts at northern and southern installations from 1 May 2013 to 1 May 2016.

Table 3. Summary statistics of the Spearman correlation between number of sightings corrected for installations crew size, environmental parameters and installations characteristics (N = 7).

Significant correlations are highlighted in bold and marked with *P ≤ 0.05, **P ≤ 0.01 and ***P ≤ 0.005.

DISCUSSION

This study adds to the existing knowledge that marine mammals are relatively frequently present around offshore oil and gas (O&G) structures (Todd et al., Reference Todd, Pearse, Tregenza, Lepper and Todd2009, Reference Todd, Warley and Todd2016; Triossi et al., Reference Triossi, Willis and Pace2013; Balle et al., Reference Balle, Clausen, Mikkelsen, Wisniewska and Teilmann2014; Arnould et al., Reference Arnould, Monk, Ierodiaconou, Hindell, Semmens, Hoskins, Costa, Abernathy and Marshall2015). A total of at least seven marine mammal species have been identified during the first three years of the Danish offshore marine mammal sighting reporting programme (MMSR), namely five cetacean species – harbour porpoise, minke whale, killer whale, white-beaked dolphin and pilot whale, and two pinniped species – harbour and grey seals. Sighted cetaceans and their relative number of observations generally reflected expected marine mammal abundance and diversity in the central North Sea (Reid et al., Reference Reid, Evans and Northridge2003; Hammond et al., Reference Hammond, Macleod, Berggren, Borchers, Burt, Cañadas, Desportes, Donovan, Gilles, Gillespie, Gordon, Hiby, Kuklik, Leaper, Lehnert, Leopold, Lovell, Øien, Paxton, Ridoux, Rogan, Samarra, Scheidat, Sequeira, Siebert, Skov, Swift, Tasker, Teilmann, Van Canneyt and Vázquez2013). Sightings of other cetacean species such as Atlantic white-sided dolphin (Lagenorhynchus acutus) and common dolphin (Delphinus delphis) close to stationary O&G installations have been reported previously in the UK (Todd et al., Reference Todd, Warley and Todd2016) and in Denmark (Steffen Sanvig Bach, personal communication).

Anthropogenic marine structures can act as artificial reefs that locally increase fish biodiversity and biomass (Pickering & Whitmarsh, Reference Pickering and Whitmarsh1997; Langhamer, Reference Langhamer2012). This has proven to be the case also for O&G installations operating at <100 m depth in the North Sea, where installations attract and concentrate a wide range of fish species (Soldal et al., Reference Soldal, Svellingen, Jørgensen and Løkkeborg2002; Fujii, Reference Fujii2015, Reference Fujii2016). These include, for example, cod (Gadus morhua), haddock (Melanogrammus aeglefinus), saithe (Pollachius virens), sand eel (Ammodytes spp.), mackerel (Scomber scombrus), sprat (Sprattus sprattus), herring (Clupea harengus) and several species of flat fish (Pleuronectid spp.), which are all known prey species for the marine mammal species observed during this reporting programme (Thompson et al., Reference Thompson, McConnell, Tollit, Mackay, Hunter and Racey1996; Abend & Smith, Reference Abend and Smith1997; Pauly et al., Reference Pauly, Trites, Capuli and Christensen1998; Olsen & Holst, Reference Olsen and Holst2001; Sveegaard et al., Reference Sveegaard, Andreasen, Mouritsen, Jeppesen, Teilmann and Kinze2012). Similarly, increased availability of prey items are associated with presence of top predators around a wide range of marine structures such as a reconstructed stony reef (Mikkelsen et al., Reference Mikkelsen, Mouritsen, Dahl, Teilmann and Tougaard2013), a large bridge (Brandt et al., Reference Brandt, Hansen, Diederichs and Nehls2014), O&G facilities (Todd et al., Reference Todd, Pearse, Tregenza, Lepper and Todd2009, Reference Todd, Warley and Todd2016; Arnould et al., Reference Arnould, Monk, Ierodiaconou, Hindell, Semmens, Hoskins, Costa, Abernathy and Marshall2015), and wind farms (Russell et al., Reference Russell, Brasseur, Thompson, Hastie, Janik, Aarts, McClintock, Matthiopoulos, Moss and McConnell2014).

Occurrence of harbour seals around southern installations at about 200 km from the closest shore is notable, as they are known typically to forage in coastal waters (Thompson et al., Reference Thompson, McConnell, Tollit, Mackay, Hunter and Racey1996; Tollit et al., Reference Tollit, Black, Thompson, Mackay, Corpe, Wilson, Parijs, Grellier and Parlane1998; Tougaard et al., Reference Tougaard, Teilmann and Tougaard2008). Observed utilization of structures or boats as a temporary haul-out location, combined with potential increased foraging success, are likely to motivate some individual seals to these longer distance offshore visits (McConnell et al., Reference McConnell, Fedak, Lovell and Hammond1999; Russell et al., Reference Russell, Brasseur, Thompson, Hastie, Janik, Aarts, McClintock, Matthiopoulos, Moss and McConnell2014; Arnould et al., Reference Arnould, Monk, Ierodiaconou, Hindell, Semmens, Hoskins, Costa, Abernathy and Marshall2015). Some seals were shown to forage actively and selectively around submerged pipelines and wind turbine structures within less than a year of their installation (Russell et al., Reference Russell, Brasseur, Thompson, Hastie, Janik, Aarts, McClintock, Matthiopoulos, Moss and McConnell2014; Arnould et al., Reference Arnould, Monk, Ierodiaconou, Hindell, Semmens, Hoskins, Costa, Abernathy and Marshall2015). This suggests the ability of marine mammals to rapidly identify and utilize these artificial habitats for foraging. Since the offshore O&G industry has been present in the North Sea for more than four decades, utilization of offshore installations as a foraging opportunity by marine mammals is therefore likely to be well-established (e.g. through social learning; Whitehead, Reference Whitehead2010).

As data presented here are based on incidental sightings, the absence of standardized design does not allow an evaluation of the absolute abundance of species (Loos et al., Reference Loos, Cooke, Deimer, Fietz, Henning and Schütte2009; Robinson et al., Reference Robinson, Jaidah, Jabado, Lee-Brooks, Nour El-Din, Malki, Elmeer, McCormick, Henderson, Pierce and Ormond2013). Nevertheless, the data could be correlated with several environmental parameters and installation related characteristics. The increasing number of harbour porpoise sightings towards the south may be related to proximity of the southern installation with areas where this species is known to occur in numbers (Gilles et al., Reference Gilles, Scheidat and Siebert2009, Reference Gilles, Viquerat, Becker, Forney, Geelhoed, Haelters, Nabe-Nielsen, Scheidat, Sveegaard, van Beest, van Bemmelen and Aarts2016; Hammond et al., Reference Hammond, Macleod, Berggren, Borchers, Burt, Cañadas, Desportes, Donovan, Gilles, Gillespie, Gordon, Hiby, Kuklik, Leaper, Lehnert, Leopold, Lovell, Øien, Paxton, Ridoux, Rogan, Samarra, Scheidat, Sequeira, Siebert, Skov, Swift, Tasker, Teilmann, Van Canneyt and Vázquez2013). Other taxonomic relationships with depth and installation aerial footprint could be explained by differences in prey availability (Pickering & Whitmarsh, Reference Pickering and Whitmarsh1997; Fujii, Reference Fujii2015). More data would be required to make these correlations species specific, and confirm their validity while accounting for possible confounding effects of other environmental factors or installation characteristics.

Most sightings reported under the MMSR were made during spring and summer. Distribution data collected from vessel and aerial surveys in the central part of the North Sea show similar temporal variations (Evans et al., Reference Evans, Anderwald and Baines2003; Gilles et al., Reference Gilles, Scheidat and Siebert2009; De Boer, Reference De Boer2010). In particular, it is suggested that a relatively higher abundance of harbour porpoise in spring and summer can be expected in the central North sea, due to seasonal porpoise population movement from coastal areas to offshore areas (Gilles et al., Reference Gilles, Scheidat and Siebert2009, Reference Gilles, Viquerat, Becker, Forney, Geelhoed, Haelters, Nabe-Nielsen, Scheidat, Sveegaard, van Beest, van Bemmelen and Aarts2016). Such seasonality in occurrence of marine mammals close to O&G platforms could be natural, and reflect a change in prey availability (De Boer, Reference De Boer2010; Sveegaard et al., Reference Sveegaard, Andreasen, Mouritsen, Jeppesen, Teilmann and Kinze2012; Fujii, Reference Fujii2015; Gilles et al., Reference Gilles, Viquerat, Becker, Forney, Geelhoed, Haelters, Nabe-Nielsen, Scheidat, Sveegaard, van Beest, van Bemmelen and Aarts2016). On the other hand, the combined effect of shorter days and harsher weather conditions significantly reduces the likelihood of detecting marine mammals based on visual surveys (Clarke, Reference Clarke1982; Teilmann, Reference Teilmann2003). Such an effect was also observed in other surveys based on incidental sightings data (Kinze et al., Reference Kinze, Jensen and Skov2003; Loos et al., Reference Loos, Cooke, Deimer, Fietz, Henning and Schütte2009). The estimation of weather corrected data would require a standardized reporting format including significantly more information (Teilmann, Reference Teilmann2003). Alternatively, long-term continuous acoustic monitoring studies (unaffected by weather and daylight hours) could help fill some of the gaps in our knowledge of seasonal distribution of marine mammals in the vicinity of anthropogenic structures.

The MMSR has proven to be a useful incentive for reporting offshore sightings. It provides us with relatively long-term marine mammal occurrence and biodiversity data in offshore O&G activity areas. The caveats associated with incidental sighting data are acceptable, as long as data analyses and inferences based on these analyses are made accordingly. Implementation of a more standardized reporting programme to gain additional knowledge on seasonality or species abundance estimates is possible (Evans & Hammond, Reference Evans and Hammond2004; Todd, Reference Todd2016). However, we predict that the additional reporting requirements would inevitably lead to a significant reduction in the number of reports from offshore working volunteers staff and a loss of valuable scientific information (Borja & Elliott, Reference Borja and Elliott2013).

SUPPLEMENTARY MATERIAL

The supplementary material for this article can be found at https://doi.org/10.1017/S0025315417000406.

ACKNOWLEDGEMENTS

We thank all offshore personnel from Maersk Oil, Hess Denmark APS and DONG Oil & Gas for their participation in the marine mammal sighting reporting programme. We also thank participating contractors: staff from Ensco 71, Energy Enhancer, Maersk Resolute as well as crew members of Esvagt Echo, Esvagt Preserver, Esvagt Preventer, Esvagt Promotor, Esvagt Server, Skandi Olympia, M/V Cecilie (FOGA APS) and M/V Anette Christina (FOGA APS) Finally, we thank G. Kaastrup, K. Povidisa, S. Taylor, V. Todd, P.G.H Evans and several anonymous reviewers for their constructive comments that improved earlier versions of this manuscript.

FINANCIAL SUPPORT

This research received no specific grant from any funding agency, commercial or not-for-profit sectors.

References

REFERENCES

Abend, A.G. and Smith, T.D. (1997) Differences in stable isotope ratios of carbon and nitrogen between long-finned pilot whales (Globicephala melas) and their primary prey in the western north Atlantic. ICES Journal of Marine Science: Journal du Conseil 54, 500503.Google Scholar
Andersen, J.H., Stock, A., Heinänen, S., Mannerla, M. and Vinther, M. (2013) Human uses, pressures and impacts in the Eastern North Sea. Technical Report from DCE – Danish Centre for Environment and Energy, no. 18, 136 pp.Google Scholar
Arnould, J.P.Y., Monk, J., Ierodiaconou, D., Hindell, M.A., Semmens, J., Hoskins, A.J., Costa, D.P., Abernathy, K. and Marshall, G.J. (2015) Use of anthropogenic sea floor structures by Australian fur seals: potential positive ecological impacts of marine industrial development? PLoS ONE 10, e0130581.Google Scholar
Balle, J.D., Clausen, K.T., Mikkelsen, L., Wisniewska, D.M. and Teilmann, J. (2014) Harbour Porpoises and Noise Around an Operating Oil and Gas Production Platform in the North Sea – Status Report. DCE.Google Scholar
Beer, T. (1996) Environmental oceanography. Boca Raton, FL: CRC Press, 402 pp.Google Scholar
Borja, A., Bricker, S.B., Dauer, D.M., Demetriades, N.T., Ferreira, J.G., Forbes, A.T., Hutchings, P., Jia, X., Kenchington, R., Marques, J.C. and Zhu, C. (2008) Overview of integrative tools and methods in assessing ecological integrity in estuarine and coastal systems worldwide. Marine Pollution Bulletin 56, 15191537.Google Scholar
Borja, Á. and Elliott, M. (2013) Marine monitoring during an economic crisis: the cure is worse than the disease. Marine Pollution Bulletin 68, 13.Google Scholar
Brandt, M.J., Hansen, S., Diederichs, A. and Nehls, G. (2014) Do man-made structures and water depth affect the diel rhythms in click recordings of harbor porpoises (Phocoena phocoena)? Marine Mammal Science 30, 11091121.Google Scholar
Clarke, R. (1982) An index of sighting conditions for surveys of whales and dolphins. Report of the International Whaling Commission 32, 559561.Google Scholar
Conrad, C.C. and Hilchey, K.G. (2011) A review of citizen science and community-based environmental monitoring: issues and opportunities. Environmental Monitoring and Assessment 176, 273291.Google Scholar
De Boer, M.N. (2010) Spring distribution and density of minke whale Balaenoptera acutorostrata along an offshore bank in the central North Sea. Marine Ecology Progress Series 408, 265274.Google Scholar
Devictor, V., Whittaker, R.J. and Beltrame, C. (2010) Beyond scarcity: citizen science programmes as useful tools for conservation biogeography. Diversity and Distributions 16, 354362.Google Scholar
Elliott, M. (2011) Marine science and management means tackling exogenic unmanaged pressures and endogenic managed pressures – a numbered guide. Marine Pollution Bulletin 62, 651655.Google Scholar
Embling, C.B., Walters, A.E.M. and Dolman, S.J. (2015) How much effort is enough? The power of citizen science to monitor trends in coastal cetacean species. Global Ecology and Conservation 3, 867877.Google Scholar
Evans, P.G.H. (1976) An analysis of sightings of Cetacea in British waters. Mammal Review 6, 514.Google Scholar
Evans, P.G.H., Anderwald, P. and Baines, M.E. (2003) UK cetacean status review. Bangor: English Nature, Peterborough and the Countryside Council for Wales, 160 pp.Google Scholar
Evans, P.G.H. and Hammond, P.S. (2004) Monitoring cetaceans in European waters. Mammal Review 34, 131156.Google Scholar
Evans, P.G.H., Pierce, G.J., Veneruso, G., Weir, C.R., Gibas, D., Anderwald, P. and Santos, M.B. (2015) Analysis of long-term effort-related land-based observations to identify whether coastal areas of harbour porpoise and bottlenose dolphin have persistent high occurrence and abundance. JNCC Report, no. 543. Peterborough: Joint Nature Conservation Committee, 147 pp.Google Scholar
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, 6982.Google Scholar
Fujii, T. (2016) Potential influence of offshore oil and gas platforms on the feeding ecology of fish assemblages in the North Sea. Marine Ecology Progress Series 542, 167186.Google Scholar
Gilles, A., Scheidat, M. and Siebert, U. (2009) Seasonal distribution of harbour porpoises and possible interference of offshore wind farms in the German North Sea. Marine Ecology Progress Series 383, 295307.Google Scholar
Gilles, A., Viquerat, S., Becker, E.A., Forney, K.A., Geelhoed, S.C.V., Haelters, J., Nabe-Nielsen, J., Scheidat, M., Sveegaard, S., van Beest, F.M., van Bemmelen, R. and Aarts, G. (2016) Seasonal habitat-based density models for a marine top predator, the harbour porpoise, in a dynamic environment. Ecosphere 7, e01367. doi: 10.1002/ecs2.1367.Google Scholar
Hammond, P.S., Macleod, K., Berggren, P., Borchers, D.L., Burt, L., Cañadas, A., Desportes, G., Donovan, G.P., Gilles, A., Gillespie, D., Gordon, J., Hiby, L., Kuklik, I., Leaper, R., Lehnert, K., Leopold, M., Lovell, P., Øien, N., Paxton, C.G.M., Ridoux, V., Rogan, E., Samarra, F., Scheidat, M., Sequeira, M., Siebert, U., Skov, H., Swift, R., Tasker, M.L., Teilmann, J., Van Canneyt, O. and Vázquez, J.A. (2013) Cetacean abundance and distribution in European Atlantic shelf waters to inform conservation and management. Biological Conservation 164, 107122.Google Scholar
Jefferson, T.A., Webber, M.A. and Pitman, R.L. (2011) Marine mammals of the world: a comprehensive guide to their identification: a comprehensive guide to their identification. London: Academic Press.Google Scholar
Kinze, C.C. (2001) Havepattedyr I Nordatlanten (Marine mammal in the North Atlantic). Copenhagen: Gads Forlag, 191 pp.Google Scholar
Kinze, C.C., Jensen, T. and Skov, T. (2003) Fokus på hvaler i Danmark 2000–2002. Copenhagen: Fiskeri- og Søfartsmuseet.Google Scholar
Koblitz, J.C., Amundin, M., Carlström, J., Thomas, L., Carlén, I., Teilmann, J., Tregenza, N., Wennerberg, D., Kyhn, L., Svegaard, S., Koza, R., Kosecka, M., Pawliczka, I., Tiberi Ljungqvist, C., Brundiers, K., Wright, A., Mikkelsen, L., Tougaard, J., Loisa, O., Galatius, A., Jüssi, I. and Benke, H. (2014) Large-scale static acoustic survey of a low-density population – estimating the abundance of the Baltic Sea harbor porpoise. Journal of the Acoustical Society of America 136, 2248.Google Scholar
Langhamer, O. (2012) Artificial reef effect in relation to offshore renewable energy conversion: state of the art. Scientific World Journal 2012, 8.Google Scholar
Loos, P., Cooke, J., Deimer, P., Fietz, K., Henning, V. and Schütte, H.-J. (2009) Opportunistic sightings of harbour porpoises (Phocoena phocoena) in the Baltic Sea at Large: Kattegat, Belt Sea, Sound, Western Baltic and Baltic Proper. In Proceedings of the 17th Meeting of the ASCOBANS Advisory Committee, Cornwall, UK.Google Scholar
McConnell, B.J., Fedak, M.A., Lovell, P. and Hammond, P.S. (1999) Movements and foraging areas of grey seals in the North Sea. Journal of Applied Ecology 36, 573590.Google Scholar
Mikkelsen, L., Mouritsen, K., Dahl, K., Teilmann, J. and Tougaard, J. (2013) Re-established stony reef attracts harbour porpoises Phocoena phocoena. Marine Ecology Progress Series 481, 239248.Google Scholar
Olsen, E. and Holst, J.C. (2001) A note on common minke whale (Balaenoptera acutorostrata) diets in the Norwegian Sea and the North Sea. Journal of Cetacean Research and Management 3, 179184.Google Scholar
OSPAR Commission (2010) Quality Status Report 2010. London: OSPAR Commission, 176 pp.Google Scholar
Palacios, D.M., Herrera, J.C., Gerrodette, T., Garcia, C., Soler, G.A., Avila, I.C., Bessudo, S., Hernandez, E., Trujillo, F. and Flórez-González, L. (2012) Cetacean distribution and relative abundance in Colombia's Pacific EEZ from survey cruises and platforms of opportunity. Journal of Cetacean Research and Management 12, 4560.Google Scholar
Pauly, D., Trites, A.W., Capuli, E. and Christensen, V. (1998) Diet composition and trophic levels of marine mammals. ICES Journal of Marine Science: Journal du Conseil 55, 467481.Google Scholar
Pickering, H. and Whitmarsh, D. (1997) Artificial reefs and fisheries exploitation: a review of the ‘attraction versus production’ debate, the influence of design and its significance for policy. Fisheries Research 31, 3959.Google Scholar
Reid, J.B., Evans, P.G.H. and Northridge, S.P. (2003) Atlas of cetacean distribution in North-West European waters. Peterborough: Joint Nature Conservation Committee, pp. 76.Google Scholar
Robinson, D.P., Jaidah, M.Y., Jabado, R.W., Lee-Brooks, K., Nour El-Din, N.M., Malki, A.A.A., Elmeer, K., McCormick, P.A., Henderson, A.C., Pierce, S.J. and Ormond, R.F.G. (2013) Whale sharks, Rhincodon typus, aggregate around offshore platforms in Qatari waters of the Arabian Gulf to feed on fish spawn. PLoS ONE 8, e58255.Google Scholar
Russell, D.J.F., Brasseur, S.M.J.M., Thompson, D., Hastie, G.D., Janik, V.M., Aarts, G., McClintock, B.T., Matthiopoulos, J., Moss, S.E.W. and McConnell, B. (2014) Marine mammals trace anthropogenic structures at sea. Current Biology 24, R638R639.Google Scholar
Soldal, A.V., Svellingen, I., Jørgensen, T. and Løkkeborg, S. (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: Journal du Conseil 59(Suppl.), S281S287.Google Scholar
Sveegaard, S., Andreasen, H., Mouritsen, K., Jeppesen, J., Teilmann, J. and Kinze, C. (2012) Correlation between the seasonal distribution of harbour porpoises and their prey in the Sound, Baltic Sea. Marine Biology 159, 10291037.Google Scholar
Teilmann, J. (2003) Influence of sea state on density estimates of harbour porpoises (Phocoena phocoena). Journal of Cetacean Research and Management 5, 8592.Google Scholar
Thompson, P.M., McConnell, B.J., Tollit, D.J., Mackay, A., Hunter, C. and Racey, P.A. (1996) Comparative distribution, movements and diet of harbour and grey seals from Moray Firth, NE Scotland. Journal of Applied Ecology 33, 15721584.Google Scholar
Todd, V.L., Pearse, W.D., Tregenza, N.C., Lepper, P.A. and Todd, I.B. (2009) Diel echolocation activity of harbour porpoises (Phocoena phocoena) around North Sea offshore gas installations. ICES Journal of Marine Science: Journal du Conseil 66, 734745.Google Scholar
Todd, V.L.G. (2016) Mitigation of underwater anthropogenic noise and marine mammals: the ‘death of a thousand’ cuts and/or mundane adjustment? Marine Pollution Bulletin 102, 13.Google Scholar
Todd, V.L.G., Warley, J.C. and Todd, I.B. (2016) Meals on wheels? A decade of megafaunal visual and acoustic observations from offshore oil & gas rigs and platforms in the North and Irish seas. PLoS ONE 11, e0153320.Google Scholar
Tollit, D.J., Black, A.D., Thompson, P.M., Mackay, A., Corpe, H.M., Wilson, B., Parijs, S.M., Grellier, K. and Parlane, S. (1998) Variations in harbour seal Phoca vitulina diet and dive-depths in relation to foraging habitat. Journal of Zoology 244, 209222.Google Scholar
Tougaard, J., Teilmann, J. and Tougaard, S. (2008) Harbour seal spatial distribution estimated from Argos satellite telemetry: overcoming positioning errors. Endangered Species Research 4, 113122.Google Scholar
Triossi, F., Willis, T.J. and Pace, D.S. (2013) Occurrence of bottlenose dolphins Tursiops truncatus in natural gas fields of the northwestern Adriatic Sea. Marine Ecology 34, 373379.Google Scholar
Whitehead, H. (2010) Conserving and managing animals that learn socially and share cultures. Learning and Behavior 38, 329336.Google Scholar
Figure 0

Fig. 1. Study area. Filled symbols show continuously manned installations and open symbols show satellite installations which are occasionally visited. Installation group names are indicated in Table 1.

Figure 1

Table 1. Danish installations overview in 2016. Construction date refers to construction of the first element of an installation which may have been expanded incrementally over the years. Areal footprint corresponds to cumulative area covered by the platform's legs at the seafloor and was estimated based on high resolution schematic drawing of the installations.

Figure 2

Fig. 2. Minke whale photographed at Halfdan A in June 2014. Note the presence of a drilling rig and a supply boat. Credit: Henrik Ærenlund Olsen (Esvagt Promotor).

Figure 3

Table 2. Summary of reported sightings from the Danish oil and gas activity area from 1 May 2013 to 1 May 2016. The summary is based on species/taxa and group size.

Figure 4

Fig. 3. Monthly marine mammal sighting counts (top) and corresponding wind speed and daylight hours (bottom). Box plots indicate civilian daylight hours median wind speed (line), 25 and 75% (lower and upper box sides) and 5 and 95% over the duration of the reporting programme (lower and upper whiskers) limits (N = 693–1698).

Figure 5

Fig. 4. Marine mammal sightings counts at northern and southern installations from 1 May 2013 to 1 May 2016.

Figure 6

Table 3. Summary statistics of the Spearman correlation between number of sightings corrected for installations crew size, environmental parameters and installations characteristics (N = 7).

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