Received: 25 December 2016
Revised: 12 May 2017
Accepted: 22 May 2017
DOI: 10.1002/aqc.2806
SUPPLEMENT ARTICLE
Identifying a network of priority areas for conservation in the Arctic seas: Practical lessons from Russia Boris Solovyev1
|
Vassily Spiridonov2
|
Irina Onufrenya3
|
Stanislav Belikov4
|
Natalia Chernova5 | Dmitry Dobrynin6 | Maria Gavrilo7 | Dmitry Glazov1 | Yuri Krasnov8 Svetlana Mukharamova9 | Anatoly Pantyulin10 | Nikita Platonov1 | Anatoly Saveliev9 | Mikhail Stishov3
|
|
Grigory Tertitski11
1
A. N. Severtsov Institute of Ecology and Evolution of Russian Academy of Sciences, Moscow, Russia
Abstract 1. The natural environment of the Arctic is changing rapidly owing to climate change. At the same
2
time in many countries including Russia the region is attracting growing attention of decision‐
P. P. Shirshov Institute of Oceanology of Russian Academy of Sciences, Moscow, Russia
3
makers and business communities. In light of the above it is necessary to protect the
WWF Russia, Moscow, Russia
biodiversity of the regional marine ecosystems in the most effective way possible, namely by
4
All‐Russian Research Institute for Environment Protection (VNII Ecology), Moscow, Russia
establishing a network of marine protected areas. 2. Identifying conservation priority areas is a key step towards this goal. To achieve it, a study based on a systematic conservation planning approach was conducted. An expanded group
5
Zoological Institute of Russian Academy of Sciences, Saint Petersburg, Russia
6
of experts used the MARXAN algorithm to produce initial results, then discussed and refined
SCANEX Group, Moscow, Russia
National Park ‘Russian Arctic’, Arkhangelsk, Russia
them to select 47 conservation priority areas in the Russian Arctic seas.
7
3. The resulting network covers nearly 25% of the Russian Arctic seas, which guarantees proportional representation of their biodiversity as well as achieving connectivity, sustainability and
8
Murmansk Marine Biological Institute Russia Federal Agency for Scientific Organizations (FASO), Murmansk, Russia
naturalness. This was largely made possible by the selected methodology, based on the MARXAN decision support tool supplemented by extensive post‐analysis that helped fill any
9
Institute of Environmental Sciences, Kazan Federal University, Kazan, Russia
10
Lomonosov Moscow State University, Moscow, Russia
gaps inevitable in the formal approach. 4. Although available data were sparse, and of varying quality and a single regionalization scheme
11 Institute of Geography of the Russian Academy of Sciences, Moscow, Russia
Correspondence Boris Solovyev, 33, Leninsky Avenue, Moscow, 119071, Russia. Email:
[email protected] Funding information Oceans 5 Foundation; WWF Netherlands; WWF Russia
1
|
could not be used (as is often the case for such areas), the selected approach has proven successful for such a large area that covers both the coastal zone and parts of the High Seas. Such an approach could be used further to identify marine protected areas throughout the Arctic Ocean.
KEY W ORDS
conservation priority areas, large marine ecosystems, marine protected areas, MARXAN, Russian Arctic seas, systematic conservation planning
I N T RO D U CT I O N
(Kudersky, 2004; Pavlov & Sundet, 2011; Spiridonov & Zalota, 2017) and sea ice habitat loss (Amstrup, Marcot, & Douglas, 2008; Moore &
The Arctic seas are experiencing significant impacts from climate
Huntington, 2008). Perhaps equally important, these changes lead to
change. The region is heating up twice as quickly as the rest of the
greater human presence in the region (Huettmann, 2012; Jørgensen
world (Alexander et al., 2013; Trenberth et al., 2007). Ice cover
et al., 2016; Wenzel et al., 2016). This could take many forms from
conditions and ocean circulation parameters are changing and these
increased oil and gas exploration and production, intensified shipping,
changes affect regional ecosystems. There are clear signs to that effect
fishing, aquaculture and tourism as well as greater military presence.
on the environmental side, such as dispersal of boreal species to the
In recent years serious efforts to protect marine biodiversity have
north (Fossheim et al., 2015; Hunt et al., 2016), biological invasions
been undertaken worldwide and the Russian Arctic seas are no
30
Copyright © 2017 John Wiley & Sons, Ltd.
wileyonlinelibrary.com/journal/aqc
Aquatic Conserv: Mar Freshw Ecosyst. 2017;27(S1):30–51.
SOLOVYEV
31
ET AL.
exception. The Arctic is receiving growing attention in Russia as
the point where it composes … 10% of all aquatic bodies under
politicians, investors, media and the general public are pushing for
the jurisdiction of the Russian Federation’ were taken into account
a comeback after the country's withdrawal from the region in the
(Strategy…, 2014, p.178). The study was based on the systematic
1990s. There are two approaches to conservation that prevail in
conservation planning approach (Margules & Pressey, 2000), and
the world today. One is based on industries regulations that are
more specifically on the framework for a pan‐Arctic network of
introduced alongside measures to protect or manage particular spe-
marine protected areas (MPAs) of the Protection of the Arctic
cies or stocks (Roff & Zacharias, 2011). The other centres on area‐
Marine Environment Working Group (PAME) of the Arctic Council
based conservation measures and is widely regarded as effective
(PAME, 2015).
(Roff & Zacharias, 2011; Spiridonov et al., 2012). In the Russian
The goal of the research was to design an ecologically connected,
Arctic the latter remains less common. The region has seven Strictly
representative and effectively‐managed network of conservation areas
Protected Natural Reserves, or zapovedniks (IUCN Ia), three National
that would protect and promote the resilience of the biological diversity,
Parks (IUCN
one Natural
ecological processes and cultural heritage of the Russian Arctic marine
Monument (IUCN III) and 41 Regional Protected Areas (IUCN Ib),
environment taking into account economic development and ongoing
but their primary purpose is to protect terrestrial ecosystems;
climate change. A network of protected areas (reserves, national parks,
coastal waters are treated as secondary, though an integral part
sanctuaries) is a set of protected areas that are geographically and
of the protected areas (PAs) (PAME, 2015). The total size of all
ecologically connected which ensures integrity, representativeness
PAs is just about 2.4% of the Russian Exclusive Economic Zone
and complementarity (IUCN, 2007; Roff, 2005).
II),
four Preserves (IUCN
IV/VI),
(EEZ) in the Arctic (Spiridonov et al., 2012). Those PAs were
The key step towards establishing a network of protected areas
established at different times separately and on an ad hoc basis,
was to identify conservation priority areas (CPAs) and see how they
and therefore it is uncertain whether or not these constitute a net-
correlate with the areas of high ecological significance/value that have
work. Their effectiveness in terms of the comprehensive protection
been formally identified in the region but for which no environmental
of the ecosystems of the Russian Arctic seas was not measured
restrictions applied. Significance or value was understood as ‘intrinsic
and assessed (Spiridonov et al., 2012).
value of marine biodiversity, without reference to anthropogenic use’
Research on the Russian Arctic marine protected areas (MPAs)
(Roff & Zacharias, 2011, p. 328). Areas of high ecological signifi-
network was launched in 2014.The existing and potential threats to
cance/value were usually larger in size than MPAs and have fuzzy
regional ecosystems as well as Russia's obligations under the Con-
boundaries (UNEP/CBD/EBSA/WS/2014/1/5 (2014)). We realize that
vention on Biological Diversity (CBD) and its national target related
meeting all these conditions, in order to develop a real network of
to Aichi target 11: ‘by 2020, the total area of terrestrial and aquatic
MPAs, is a tremendous task and at this early stage is not a network
territories with regulated resource use policies and which play a
as in the above meaning but rather a coherent set of areas as first
key role in the provision of ecosystem services is increased to
defined by J. Ardron (cited after Roff & Zacharias, 2011, p. 344). We,
FIGURE 1
The bathymetry of the Eurasian sector of the Arctic Ocean with borders and boundaries used to define the search area
32
SOLOVYEV
ET AL.
however, use the term ‘network’ throughout the text emphasizing
water mass (the core of which has high salinity >34.5 psu) enters the
that this is yet not an ideal network derived from the theory of
Arctic in two ways: with the coastal current along the continental land
conservation biology.
in the Barents Sea, and from the north in the intermediate layer (100–
The purpose of this paper is to demonstrate how the methodol-
300 m) between Spitsbergen and Franz Josef Land archipelagoes, in the
ogy of identification of CPAs could be applied in the Arctic and
troughs of the northern Kara Sea, and in the Laptev Sea slope (Dmitrenko
examine a possible configuration of a network of priority areas for
et al., 2006; Rudels, 2015; Seidov et al., 2015; Zalogin & Kosarev, 1999).
conservation in the Arctic seas, which is a vast, poorly studied, highly
The water masses of the Siberian shelf, strongly influenced by
dynamic region for which only sparse data are available and to draw
river discharge consist of two cores (river runoff derived waters)
some practical lessons for future planning of the conservation efforts
bounded by the 25 psu isohaline: in the Kara Sea at the mouth of
both in the Polar Regions and in the High Seas.
the rivers Ob’ and Yenisei, and in the Laptev and East Siberian seas. The maximum expansion of the freshened water masses takes place
2 EURASIAN ARCTIC SEAS ENVIRONMENT A N D BI O G E O G R A P H Y |
in summer while the minimum is observed in late winter; there is also significant variation related to meteorological situations (Bauch, Dmitrenko, Kirillov et al., 2009; Bauch, Dmitrenko, Wegner et al.,
Russia's internal marine waters, territorial sea, the EEZ and the conti-
2009; Dobrovolsky & Zalogin, 1982; Seidov et al., 2015; Zalogin &
nental shelf encompass most of the Eurasian Arctic seas except the
Kosarev, 1999; Zatsepin, Kremenetskiy, Kubryakov, Stanchny, &
western Barents and the Norwegian Seas (Figure 1). The Barents, Kara,
Soloviev, 2015).
Laptev, East Siberian and Chukchi shelf seas, and the semi‐landlocked
The Pacific water mass is best defined by the 0°C surface
White Sea are part of the Arctic Ocean. The Bering Sea belongs to the
isotherm in June before the water column warms up in summer. In
Pacific Ocean. The boundaries of the Eurasian Arctic seas are demar-
winter
cated by conventional borders or by the islands and archipelagos. Most
(Dobrovolsky & Zalogin, 1982; Rudels, 2015; Seidov et al., 2015;
of the Eurasian Arctic sea area (and in some cases entire seas) is located
Zalogin & Kosarev, 1999).
on the continental shelf where water depth exceeding 200 m is not common (except for the Barents and the Laptev Seas) (Figure 1). The Eurasian Arctic seas represent an open area where four core water masses are advected from the outside (Figure 2). The Atlantic
FIGURE 2
this
water
mass
undergoes
complete
transformation
The distribution of the Arctic water mass is defined by the −1°C surface isotherm. This water mass is characteristic for the circumpolar Arctic Ocean (Dobrovolsky & Zalogin, 1982; Rudels, 2015; Zalogin & Kosarev, 1999).
Location of core water masses (A, C, D, E, P) and the main frontal areas (A/C, D/B, D/C, E/C, P/C) and particular types of transformed waters (at, Ct, W) in the Eurasian sector of the Arctic Ocean. Schematic map prepared by Pantyulin and Chuprina (2015) based on Boyer et al. (2012) A/C – Atlantic and Arctic water frontal area, D/B – Barents Sea and river runoff derived water in the Kara Sea frontal areas, D/C – Arctic and river water in the Kara Sea, E/C – Arctic and river runoff derived water in the east Siberian and the Laptev seas, P/C – Pacific and Arctic water, At – Transformed Atlantic waters, Ct – Transformed Arctic waters, W – White Sea waters. Transformed coastal water masses are not shown
SOLOVYEV
33
ET AL.
Water masses of particular seas undergo various transformations.
landfast ice that forms specific marine habitats (Carmack et al.,
Frontal transformation in the areas of contact between core water
2006). The extent of landfast ice varies significantly in different
masses is of particular importance for the purpose of this study. In this
regions, ranging from tens of metres to hundreds of kilometres
regard the frontal zone between the Atlantic and Arctic waters, i.e. the
(Figure 3).
so called Polar Front can be defined using both temperature and
Flaw polynyas are extensive areas of open water or of new unsta-
salinity gradients (Figure 2 A/C) (Dobrovolsky & Zalogin, 1982; Loeng,
ble ice that are regularly formed in particular areas during the winter
1991; Rudels, 2015; Seidov et al., 2015; Zalogin & Kosarev, 1999).
season between landfast ice and close pack ice (Figure 3). The
The frontal zone between the waters influenced by river discharge
polynyas in the Siberian shelf are formed as a result of specific atmo-
and the Arctic waters is defined using steep gradients of surface salin-
spheric processes, in particular regular winds pushing drifting ice off-
ity (between 25‰ and 30‰). Two such zones are delineated. The
shore (Popov & Gavrilo, 2011; Zakharov, 1996). Zakharov (1966,
western one is the contact area of the Ob’–Yenisey waters and the
1996) called polynyas ‘ice factories’, highlighting the fact that up to
Arctic waters in the Kara Sea (Figure 2 D/C), defined for the purposes
70% of the total volume of sea ice developing in the Arctic seas may
of the present study as the Kara Front. The eastern one is located in
be produced in polynyas. In spring and in summer polynyas accumulate
the northern part of the Laptev and East‐Siberian seas where the Lena
heat and become centres of seasonal sea ice decay (Zakharov, 1966,
and Indigirka rivers water contacts the Arctic water mass (Figure 2 E/C)
1996). They are considered to be extremely important for the Arctic
(Bauch, Dmitrenko, Kirillov et al., 2009; Bauch, Dmitrenko, Wegner
marine biodiversity and ecosystem (Carmack et al., 2006; Kupetsky,
et al., 2009; Dobrovolsky & Zalogin, 1982; Zalogin & Kosarev, 1999).
1961; Spiridonov, Gavrilo, Krasnova, & Nikolaeva, 2011).
The contact zone between the Pacific and the Arctic waters (Rudels,
In the last two decades there were hardly any areas in the Eurasian
2015) is located in the northern Chukchi Sea (Figure 2 P/C). It can be
Arctic seas where high concentrations of multiyear sea ice persisted
defined by the summer surface temperature.
from year to year; furthermore most of the Eurasian Arctic seas
In addition, there are transformed water masses which bear
became ice free by September (Frolov, Gudkovich, Karklin, Kovalev,
unique characteristics, i.e. the Barents Sea water (cooler than the
& Smolyanitsky, 2009; Jeffries, Richter‐Menge, & Overland, 2015;
Atlantic water mass but retaining the high salinity of the latter)
Maslanik, Stroeve, Fowler, & Emery, 2011). However, in particular
(Dobrovolsky & Zalogin, 1982; Loeng, 1991; Zalogin & Kosarev,
areas sea ice massifs can persist during sea ice decay thus maintaining
1999) and the smaller areas of particular bays, straits (Pantyulin,
marginal ice zone conditions for a prolonged time and influencing pro-
2012) and troughs (Zatsepin, Poyarkov et al., 2015).
ductivity and other ice related processes (Gavrilo & Spiridonov, 2011).
While the western and the south‐western parts of the Barents Sea
Biogeographic regionalization of the Russian Arctic may be well
are ice‐free all‐year round because of the inflow of the Atlantic water,
represented by respective schemes for macrozoobenthos (Petryashov
other Russian Arctic waters freeze in winter. Significant parts of the
et
coastal zone of the Russian Arctic seas are seasonally covered with
Redkozubov, & Petryashov, 2015). This regionalization system is in
al.,
2010,
2013;
Spiridonov,
2011;
Spiridonov,
Vedenin,
FIGURE 3 Location of landfast ice and flaw polynyas in the Eurasian Arctic seas (excluding the Bering Sea) in 2000–2015 mapped on the basis of satellite images (Dobrynin, 2015)
34
SOLOVYEV
ET AL.
many respects similar to the scheme of ichtyogeographical regionaliza-
Marine Ecosystems (AMAP/CAFF/SDWG, 2013 via ArkGIS, WWF's
tion (Chernova, 2011) and overlaps with the phytogeographic regional-
map portal for the Arctic). In the case of an overlap, the northern-
ization scheme for macroalgae (Zinova, 1974). Benthic biogeographic
most border was selected. The south‐eastern boundary of the
boundaries reflect the influence of environmental factors at different
research area was on the Navarin Cape latitude in the Bering Sea
spatiotemporal scales while planktonic boundaries are in many ways
to the south of the Anadyr Bay and the Chirikov Basin as this is
similar but usually have higher spatial resolution (Mokievsky, 2009).
where the border between temperate Northern Pacific and Arctic
Main biogeographic provinces roughly correspond to distribution of
realms lies (Spalding et al., 2007). On land the research area was lim-
core water mass. The Eurasian Arctic Province is associated with the
ited by the sea–land border, though technically it expanded inland,
Arctic water mass and the Atlantic water mass in deeper layers; the
the land‐based units were disregarded in the analysis (Figure 1).
Amerasian Arctic Province corresponds to the Arctic water not under-
The estuaries of the biggest rivers (the Ob’ and the Yenisei rivers)
laid by the Atlantic water; the Siberian Shelf Province reflects the influ-
were included in the research. Total area of research was over 6
ence of the river runoff derived water. The advection of the Atlantic
million km2, which is 2.5 times bigger than the Mediterranean Sea.
water in the Barents Sea and the Pacific water in the Chukchi Sea
The Lambert azimuthal equal‐area projection with central meridian
are reflected in the extensive biogeographic transitional zones in the
100°E based on WGS84 ellipsoid was used.
Barents and the Chukchi–East Siberian Seas. Distinct biogeographic districts are present in the White Sea and some other coastal areas owing to peculiar oceanographic conditions, including freshwater influ-
3.2
|
Environmental characteristics in the analysis
ence, and sea ice regime (Naumov, 2001; Petryashov et al., 2010;
The bathymetric conditions of the Eurasian Arctic seas are diverse and
Spiridonov, 2011; Spiridonov et al., 2015).
contrasting (Figures 1 and 2). Bathymetry data were often used as surrogates of benthic habitats (Table 1; Supplementary material).
3
METHODS
|
The study was based on existing data, both published and unpublished (e.g. remote sensing data). MARXAN software (Ball & Possingham, 2000) was selected as a decision support tool to structure and process data and assist experts in identifying the high conservation priority areas. The research was conducted by a team of experts from a number of Institutes of the Russian Academy of Sciences, the leading Universities and research centres and coordinated by the WWF Russia. The work was organized around a series of workshops. In between meetings experts continued to work individually and in groups. The main phases of the research included: 1. Defining basic parameters of the analysis: area of research, scale of processes and units and conservation features. 2. Collection, validation and compilation of data and definition of targets.
Polynyas, fast ice, areas of icebergs distribution and high concentration of multiyear ice zones were mapped using remote sensing data. Images produced by various satellites were used: LANDSAT‐5, LANDSAT‐7 (2005–2015, 563 images processed and 43 decoded), AMRSE, AMRSE‐2 (2000–2014, over 7000 images processed and 208 decoded), MODIS‐TERRA, MODIS‐AQWA (2007–2015, 784 images processed and 51 decoded). Mapping was done at 1:500 000 scale using Mapinfo v 8.2 Scanex Geomixer v 2.31, Scanex Image Processor v. 4.25.1 software. The spatial distribution of results of the supervised classification was used for preparing learning data for different spectral bands. Estimated signatures were used for seasonal mapping with post‐process verification of accuracy. Regions with prevailing distribution were selected (Dobrynin, 2015). Information on polynyas, extensive landfast ice areas (Figure 3) or areas of prolonged conditions of the marginal ice zone (MIZ) were used directly to define conservation features (CFs) or as surrogate data for inferring biological CFs, such as wintering areas of Laptev Sea walruses
3. MARXAN analysis and calibration of its parameters.
(which can hardly be found outside polynyas since this population does
4. Post‐MARXAN analysis, expert verification and interpretation of
not leave the Laptev Sea in winter). Major frontal zones were defined on the basis of the NOAA
results.
Arctic Regional Climatology atlas (by Boyer et al., 2012; Seidov Research was done in 18 months from the first meeting to the presentation of the final results.
et al., 2015; see Figure 2, Table 1). The frontal zones and the multiyear ice zones contributed to decreasing the cost of cells in the MARXAN analysis (see 3.9 Cost Layer).
3.1
|
Research area
The research covered those parts of Arctic seas under Russian juris-
3.3
|
Selected scale of processes and units
diction: the eastern part of the Barents Sea, the White Sea, the Kara
The research area was divided into 6674 planning units (PUs) –
Sea, the Laptev Sea, the East‐Siberian Sea, the western part of the
square cells with a side length of 30 km. This scale was determined
Chukchi Sea and the north‐western part of the Bering Sea
by the quality of data available for analysis and the scale of pro-
(Figure 1). The research area on the east and the west was limited
cesses under analysis. For the purpose of unification and compila-
by borders with Norway and the USA respectively. The northern
tion, all vector data layers of different quality were transformed
boundary of the research area was the edge of the Russian exclusive
into a raster on the more detailed grid composed of 5 × 5 km cells
economic zone (EEZ) and the northern limits of the relevant Large
nested into the 30 × 30 km network.
SOLOVYEV
TABLE 1
35
ET AL.
Criteria for selection of conservation features and examples
General criterion
Examples of specific conservation objectives
Number of CFs
Protection of rare communities of Zostera, especially in the Arctic seas outside the White Sea
16
Zostera communities, Ramsar zones, polynyas
Special importance for life‐history Protection of breeding/foraging, feeding ranges and stages of species migration corridors of particular rare species and species maintaining ecosystem functions and structures
72
Arctic cod spawning grounds, gray whale summer concentrations
Importance for threatened, Protection of ranges of species listed in IUCN red endangered or declining species list and Russian red data book and/or habitats
44
Ivory gulls colonies, Atlantic population bowhead whale range, Greenland shark range
Vulnerability, fragility, sensitivity or slow recovery
Protection of walrus rookeries at the seasons when walruses are present there
15
Laptev walrus rookeries, sponges concentrations
High biological productivity
Protection of areas of high productivity in the marginal ice zone
13
Kittiwake and Brünnich's guillemot wintering areas, marginal ice zone
High biological diversity and naturalness
Protection of areas of high benthic diversity associated with kelp communities
12
Matochkin Shar Strait kelp community, Zostera communities
Representativeness
Protection of a share of each phytogeographic region in the Russian Arctic seas
79
Trenches of the Kara and Barents Seas brackish waters communities, Eurasian province of Arcto‐Atlantic phytogeographic region
Genetic diversity
Protection of each geographical population of kittiwake/protection of kittiwake ranges in each of the Russian Arctic seas
65
Distribution of kittiwake in the Barents Sea, Macoma calcarea communities
Maintenance of ecosystem functions/structures
Protection of habitats/ranges of common, abundant species of birds
79
Common eider range, ringed seal habitat preference, polynyas
33
Nawaga spawning grounds, Pacific walrus whelping patches
Uniqueness or rarity
Areas/species important for local, Protection of habitats of marine mammals hunted by including indigenous population indigenous population of Chukchi region
3.4
|
Conservation features: Criteria for selection
Examples
invertebrates was also used for a general assessment of biogeographic representativeness of the resulting CPAs network.
For the purpose of the project, conservation features (CFs) were iden-
Types of habitat were defined by geomorphological (i.e. bottom
tified as spatially definable components of biodiversity and ecological
topography, coastline), sedimentological and oceanographical (includ-
processes, such as species and populations ranges, key habitats, com-
ing tidal regime and polynyas) characteristics. In addition, several CFs
munities' biotopes and locations of special zones/features. Conserva-
representing specific benthic communities dominated by one or sev-
tion features were selected in a broad context (Ball, Possingham, &
eral macroinvertebrate species and distributed over extensive areas
Watts, 2009). The following criteria for ecologically and biologically
were selected (Denisenko, Sirenko, Gagaev, & Petryashov, 2010; Kiyko
significant areas (EBSAs) were used to select conservation features:
& Pogrebov, 1997; Petryashov et al., 2010).
uniqueness or rarity, special importance for life‐history stages of
Distinctive benthic CFs included areas with increased benthos
species, importance for threatened, endangered or declining species
biomass at the scale of a particular sea, some remarkable systems of
and/or habitats, vulnerability, fragility, sensitivity or slow recovery,
benthic habitats such as fjordic lagoons and communities, seagrass
biological productivity, biological diversity and naturalness (Skjoldal &
meadows that seldom occur in the Arctic and endemic kelp of the
Toropova, 2010; UNEP/CBD/COP/DEC/IX/20, 2008). To achieve
Matochkin Shar Strait in Novaya Zemlya (Flerov, 1932). Areas with a
the goal of the project four additional criteria were added: representa-
high concentration of indicators of vulnerable marine ecosystems
tiveness, genetic diversity (representativeness at the population level),
(VME as defined by the FAO (2009)) that occur in the Barents Sea,
maintenance of ecosystem functions/structures, and areas/species
the White Sea and the Kara Sea were also included as separate CFs.
important for indigenous peoples (Table 1).
Conservation features for vertebrates were presented as spe-
Experts independently selected CFs for benthos, fish, seabirds and
cies ranges in general, i.e. for keystone, common and abundant,
marine mammals (for sources of data see Table S1) (Table 1) and then
commercial and endangered, threatened or protected (ETP) species
discussed and corrected the lists during a series of workshops and
of fish, mass and ETP species of seabirds and marine mammals
through MARXAN analysis.
and as distinctive parts of their distribution ranges such as breed-
Benthic CFs were selected primarily to represent biogeographical units and habitat types. They therefore included biogeographic
ing, foraging and other important areas (mostly for vertebrates) (Table 1; Table S1).
provinces as spatial proxies of flora (for macroalgae, Zinova, 1974)
Several CFs were defined for some species. For instance, there are
and fauna both for benthic invertebrates (Petryashov et al., 2010,
three different populations of walruses in the research area and their
2013; Spiridonov, 2011; Spiridonov et al., 2015) and fish (Chernova,
haul‐out sites and whelping patches were counted as separate CFs
2011). The present biogeographic regionalization scheme for benthic
with specified amounts, weights, targets and other parameters.
36
SOLOVYEV
ET AL.
Conservation features covered different levels of biodiversity.
opinions. Both direct data on CFs distribution and its surrogates were
Several CFs related to particular and often specific populations of cer-
used for analysis, e.g. data on fast ice distribution were used as a
tain species thus covering the population level, i.e. the particular pop-
surrogate for the distribution of ringed seal whelping patches.
ulations of the Atlantic salmon, the common eider, the beluga whale,
Metadata describing data sources, methods of collection, quality, time
the Atlantic and Pacific walrus and different populations of the polar
period and other characteristics for each dataset were also collected
bear. This situation mostly applies to vertebrates but also to the geo-
(Table S1).
graphically separated populations of seagrass (Zostera marina). For most of the selected seabirds and marine mammals, as well as for several fish species, the study aimed at conservation of species in the Arctic by protecting their habitats and thus covered the species level. At the community level entire areas hosting spatial complexes of different benthic and (indirectly) pelagic communities including those in fjords, fjordic lagoons, lagoons of accumulative origin, estuaries, shelf banks and troughs and coastal zones of archipelagoes were considered. Finally by inclusion of biogeographical regions the research considered the level of distinct floras and faunas (for macroalgae,
3.6
|
Data quality, gaps in data
Experts assessed the quality of each dataset as ‘low’, ‘medium’ or ‘high’ depending on data credibility that comprised data accuracy, method of collection, and time of data collection (Figure 4). Distribution of the number of layers and their quality per unit is presented on Figure 4. A Data Coverage Index was calculated as the number of layers multiplied by the quality index, with high quality datasets having index 3,
benthic invertebrates and fishes, see above).
medium – 2, and low – 1.
3.5
3.7
|
Data sources, types, and rejected data
|
Weights of datasets
Data on CFs distribution were presented as shape‐files; one shape‐file
All datasets were weighted for MARXAN analysis. The weight of each
per CF. Data were collected by experts on the region and taxonomic
CF was based on its data quality, number of objectives it met and type
groups.
of data it contained (surrogate or direct).
About 300 datasets were compiled; more than 80 of them were
Initially each dataset received the highest possible weighting –
rejected as inappropriate or redundant for the purposes of the
100. Then it was decreased according to criteria listed below
research and weren't used directly (Table S1 ‘Rejected data’). The
(Table 2). After a number of MARXAN tests some weights were
number of datasets used for MARXAN analysis varied from test to
adjusted by the expert team. All the changes of the weights were doc-
test; in the final test 195 layers were analysed.
umented (see Table S1). For example, Laptev walrus haul‐out sites on
Data were collected from different sources: direct field surveys, remote satellite surveys, modelling or as spatially presented expert
FIGURE 4
ice got weight 80, because the dataset quality was low, it satisfied five criteria and was based on results of field surveys – direct data.
Data coverage index distribution: Density of data layers used in analysis weighted by data quality
SOLOVYEV
TABLE 2
37
ET AL.
Weighting criteria for datasets
Quality
Number of criteria
Type of data
areas (Ball & Possingham, 2000). All data layers were created, orga-
Low
Medium
High
nized and processed as shape‐files using ArcGIS 9.2 (ESRI, 2006) and
−20
−10
0
QGIS 2.6.1 (Quantum GIS Development Team, 2014). ‘ESRI Shapefile’
1
2–3
>4
‐20
−10
0
Surrogate
Direct
‐10
0
format was applied for ‘points’, ‘lines’ and ‘polygons’ geometries. R package ‘rgdal’ was used to import/export ESRI Shapefiles (Bivand, Keitt, & Rowlingson, 2016). After that the data were prepared for MARXAN analysis: special scripts were written in the R programming language using GDAL library (GDAL, 2016; R Core Team, 2016). Other scripts for MARXAN analysis calibration and post‐analysis were also
3.8
Conservation targets
|
written using GDAL library.
As there is no solid scientific basis to access basic sufficiency of a conservation feature representation in the network of protected areas (Margules, Pressey, & Williams, 2002), the Aichi Target 11 (10%) was used as a basic conservation target (minimum share of a CF within the network of protected areas) (CBD, 2010). Doubled Aichi Target 11 (20%) was used as the conservation target for rare and unique species as well as for areas of special importance for life‐history stages of keystone species. After the first series of MARXAN tests and calibrations, experts decided to raise targets for some CFs, for example the target for Zostera communities outside the White Sea was set at 100%. All weights and targets are presented in Table S1.
3.11
|
MARXAN analysis
Repeated MARXAN runs were performed with different scenarios to define a range of options regarding the parameters and the location of potential priority areas. The team of experts reviewed the options proposed on the basis of MARXAN runs and eventually approved the final list by consensus. One of the benefits of MARXAN analysis is that it is an iterative process that can be repeated after data and parameters are added or corrected. Six full test cycles were conducted; results of each cycle were analysed during expert workshops. Each cycle included calibration and looked into a number of scenarios in search of conservation
3.9
Cost layer
|
priority areas. Calibration was intended to test certain technical param-
The cost of each PU was defined primarily by its area. Apart from area,
eters of the project including the number of iterations, boundary
particular oceanographic characteristics could influence cost of some
length modifier (BLM) and species penalty factor (SPF) (Ardron,
PUs. Coefficients lowering cost were set for the areas of major fronts
Possingham, & Klein, 2010; Ball & Possingham, 2000).
(which were used as surrogates for potential areas of high diversity and
The number of iterations was calibrated to identify the number
productivity) and for the areas of multiyear ice distribution (Table S1).
sufficient for MARXAN to provide an efficient solution. BLM regulated
Coefficients were defined after a series of MARXAN tests and calibra-
clumping of the solutions, while the SPF was used to determine the
tions by the expert team.
significance of CF individual weights in the analysis and helps MARXAN reach all project targets (Ardron et al., 2010).
3.10
|
Software
The optimal number of iterations was determined as 50 × 106. Optimal BLM and SPF were identified through calibration and visual
Geographic Information Systems (GIS) software and the decision sup-
analysis by the expert team and set at 0.3 and 0.04 respectively
port tool MARXAN were used to define and map conservation priority
(Figure 5).
FIGURE 5 Calibration of BLM and SPF used in Marxan project: A) in relation to the number of PUs (planning units) B) in relation to the missing values (CFs)
38
SOLOVYEV
TABLE 3
ET AL.
MARXAN analysis scenarios
Number
Name of the scenario
1
Basic: Normal targets, all CFs included in the analysis
2
Basic + existing PAs included in the analysis
3
Only existing PAs included in the analysis
4
Normal targets and basic parameters but only the CFs providing ecological functions included in the analysis
5
Normal targets and basic parameters but only the CFs representing rare and endangered species, populations, habitats and ecosystems included in the analysis
6
Normal targets and basic parameters but only the CFs providing representativeness functions included in the analysis
7
High targets scenario
By design MARXAN is not a decision‐making, but a decision‐
After all calibrations and corrections the following scenarios were used to determine the conservation priority areas (Table 3).
support tool (Ardron et al., 2010). In the project it was used to
Scenario 1 (Basic) was intended to show the distribution of
facilitate setting goals and targets, data handling and processing.
potential priority conservation areas. Scenario 2 showed the effi-
After six cycles of analysis the expert team considered the machine
cient distribution of these areas and took into account the existing
analysis sufficient. A broader team of experts then reviewed and
PAs. Outputs of these scenarios (total size of the conservation
corrected the configuration of the network proposed by MARXAN.
priority areas, number of targets achieved) along with outputs of
The team consisted of both experts that initially worked on the
Scenario 3 demonstrate the effectiveness of the proposed network
project and those that joined later. Results provided by MARXAN
in comparison with the existing PAs.
were carefully reviewed through a series of six workshops.
Scenarios 4–6 were intended to demonstrate to which of the
As a result the map of conservation priority areas was produced
criteria the selected areas mostly contributed: conservation of key-
(Figure 9) with lists of CFs supposed to be protected in each of 47
stone species providing ecological functions, protecting rare and
selected areas. For each selected area these CFs were ranked as ‘very
endangered species, or providing representativeness. The purpose
important’, ‘significant’ and ‘others’.
of Scenario 7 was to check if increasing targets would augment the size of originally selected areas or result in emergence of new priority areas.
4
3.12 | Post‐analysis: Ecological and geographical connectivity, representativeness, naturalness and stability
4.1
As MARXAN isn't able to fully incorporate the connectivity factor
Figure 7.
RESULTS
|
|
MARXAN analysis
Results of the final scenarios 1–7 are presented in Figure 6, with the basic scenario (Scenario 1) outputs presented in the more detailed
(Ardron et al., 2010; Roff & Zacharias, 2011), the assessment was per-
The total area of the best solution provided by MARXAN in the
formed by experts. They analysed ecological and geographical connec-
basic Scenario 1 was 771 924 sq km or 16.73% of the Russian Arctic
tivity for each of the CFs and made necessary corrections to the data
seas area. All 195 conservation targets were achieved in this solution
before the final runs. For the purpose of the research, connectivity
and most of them exceeded the minimum set targets (Figure 8). The
was interpreted as both an ecological and a geographical factor; the
resulting distribution of conservation priority areas showed that the
ecological dimension covered trophic connections, e.g. beluga whale
biggest areas were located in the central part of the research area.
and Arctic cod are supposed to be protected in the same area, while
Smaller but more numerous areas were located in the western and
the geographical factor accounted for connections between different
the eastern seas – the White Sea, the Barents Sea, western part of
habitats of the same species/population: feeding areas, whelping areas
the Kara Sea, the Chukchi Sea and the Bering Sea. The areas in the
and migration corridors between them.
East‐Siberian Sea were the smallest in size and number. Most of the
Another factor that experts analysed during the post‐analysis was
areas were attached to a shoreline or located in the vicinity of the shore.
representativeness. The aim of this exercise was to make sure that all
Results of additional Scenario 2 demonstrated that including
species and populations were presented in the selected areas of differ-
existing protected areas in a result ‘by default’, i.e. locking PUs within
ent geographical regions.
existing PAs into the output, only changed the configuration of
The criterion of naturalness was used to make sure that areas
selected PUs insignificantly by increasing the number of selected PUs
selected as important for CFs did not overlap with areas of anthropo-
in the areas around existing PAs. Total area of the best solution in this
genic pressure and that the most natural areas possible were selected.
scenario was 17.2% of the Russian Arctic seas which is just 0.5% more
The redundancy check was intended to make sure that each CF
than in the scenario where PAs are not taken into account. Only
was represented in at least two different areas, as that would provide
existing protected areas were included in the resulting configuration
additional protection in case of a disaster in one of the areas.
in Scenario 3.
SOLOVYEV
FIGURE 6
39
ET AL.
Results of scenarios (1–7) presented as distribution of PUs selection frequency
Scenarios 4 to 6 demonstrated to which criteria selected areas mostly contribute: conservation of keystone species providing ecological functions, protecting rare and endangered species, or providing representativeness. Some areas such as Franz Josef Land waters or
of the same archipelago that provides for conservation of rare features and species.
4.2
|
Conservation priority areas
the common outer frontal area of the Ob’ and Yenisey river mouths
Conservation priority areas that resulted from MARXAN and post‐
in the Kara Sea, generally ice‐free coastal areas of the north‐western
MARXAN analyses are presented in Figure 9. The breakdown of areas
part of the Kola Peninsula were selected as providing all three types
by particular marine basins and quantitative coverage characteristics of
of functions in a potential system of conservation priority areas. Most
the defined areas are summarized in Table 4.
of the areas contribute to two out of three: e.g. coastal waters of
The total size of the areas calculated through the experts' analysis is
north‐eastern Novaya Zemlya are important for conservation of key-
1 145 117 km2 or 24.8% of the Russian Arctic seas. Forty‐seven areas
stone and rare species and features, as well as the shallow shelf around
were identified. Their size varied from 96 to 88 920 km2 (Table 3).
the Lena River delta providing protection for endangered species and is important for representativeness of a potential network of MPAs.
Shares of CFs included in the network of conservation priority areas by far exceeded the previously established conservation
Some of the selected areas were significant only for one of the
targets: average target for a CF was established as 16.6% and
functional groups, like coastal waters of the Severnaya Zemlya archi-
included in the network as 36.6% (median is 20% and 30.85%
pelago that provides representativeness, or the area to the north‐east
respectively) (Figure 8).
40
FIGURE 7
SOLOVYEV
ET AL.
Distribution of proposed conservation priority areas, MARXAN: Scenario 1, PUs selection frequency
FIGURE 8 Distribution of conservation targets: Initial, achieved with existing PAs, achieved with MARXAN best result and the experts' choice conservation priority areas
5 | D I S T R I B U T I O N A N D SI Z E O F T H E PRIORITY CONSERVATION AREAS IN R E LA T I O N T O P A R T I C U L A R S E A S
areas in the Laptev Sea and the Bering Sea are also large. The CPAs in the White Sea are smaller than in any other sea including the smallest CPA in the entire Russian Arctic (96 km2). In spite of the differences between the seas, the total coverage of CPAs is
The greatest number of conservation priority areas (CPAs) was
roughly similar and for most seas is within the range 23–38%, or
identified for the Barents Sea (17) and the smallest for the Laptev
from a quarter to a third of the sea surface area. Only the East
Sea, Chukchi Sea and the north‐western Bering Sea (5) (Table 4).
Siberian Sea has a smaller coverage, at 16%. The CPAs of the
The Barents Sea was also characterized by the greatest range and
above‐mentioned seas have similar ratios of important and most
the largest of the areas (nearly 90 000 km2), while the smallest
important CFs.
SOLOVYEV
FIGURE 9
41
ET AL.
Conservation priority areas resulted from MARXAN and post‐MARXAN analyses
In the Barents Sea, areas 1–4 were nested within the generally ice‐
frontal area with frequent polynya events (26) and Baidaratskaya
free coastal realm of the Kola Peninsula representing different sea-
Guba (24) receiving less freshwater input. In the western part of
scapes, oceanographical conditions and biogeographical divisions
the sea, area 15 is located in the Kara front separating the Barents
along the direction of the peninsula coastal currents. Area 5 encom-
Sea and the Kara Sea waters in the St. Anna Trough and also includes
passes mostly shelf areas influenced by complex frontal systems on
the northernmost coastal areas of Novaya Zemlya. Area 25 encom-
the boundary between the Barents and the White Seas. Areas 21–23
passes fjords of the eastern coast of Novaya Zemlya, the deep and
are coastal areas of the shallow south‐eastern part of the Barents
narrow Matochkin Shar Strait separating the north and the south
Sea and cover most of the bays having various oceanographic and
Islands of the archipelago, and the eastern Novozemelskiy Trough.
sea ice characteristics. Areas 16, 17 and 19 are coastal areas of the
In the east, extensive areas represent the eastern shallow shelf of
west coast of Novaya Zemlya Archipelago with its skerries and various
the Kara Sea with numerous islands, a long lasting sea ice season
types of fjords. Areas 18 and 20 are representative areas of the eastern
and extensive fast ice (31), the waters of the Severnaya Zemlya archi-
Barents shelf with its banks (in particular Geese Bank) and troughs
pelago with associated fast ice and polynyas (30), and the area of
influenced by cold inflow from the Kara Sea (18), convergence of cold
Voronin Trough and the Kara Sea slope (29).
and warm currents and local upwelling (20). Area 12 represents
In the Laptev Sea the analysis resulted in selecting four areas.
troughs and banks of the northern Barents Sea and a characteristic
The western most area (32) covers the coastal zone of the east
segment of the Polar Front, while areas 13 and 14 reflect conditions
coast of Taymyr Peninsula and the western part of the Great
of waters around most high latitude Arctic archipelagoes in the
Siberian Polynya; the central area (33) is located on the shallow
Eurasian sector, Franz Josef Land (with Victoria I.) along with adjacent
shelf around the Lena River delta, also overlapping with part of
shelf and slope. The size of areas in the Barents Sea generally increases
the Great Siberian Polynya region. The eastern areas (34, 35) are
from the coastal to offshore zone and from the south to the north, with
located on the border between the Laptev and the East Siberian
areas 12 and 13 being among the largest selected areas.
seas to the north of the New Siberian Islands, also covering
The White Sea is represented by the areas which reflect a high variety of CFs over this relatively small marine basin. Areas 6, 9, and
polynyas and the waters around the most remote small high Arctic islands (De Long Islands in the East Siberian Sea).
11 encompass important structural divisions of the sea: Gorlo, the
Other conservation priority areas are located in the east of the
strait connecting its outer and inner parts (6), the deep Kandalaksha
East Siberian Sea. They include most of Chaun Bay (Chaunskaya Guba)
Bay with internal trough (9) and shallow Onega Bay with the Solovki
(36) and De Long Strait (39) along with the coastal zone and shallow
Archipelago (11). Areas 7, 8, and 10 are smaller coastal areas associ-
shelf areas around Wrangel Island in the boundary area with the
ated with particular bays and lagoons.
Chukchi Sea. In the Chukchi Sea proper the analysis revealed two
In the Kara Sea, shallow coastal areas represent the huge estuarine systems of Ob (27) and Yenisei (28) with their common outer
extensive shelf areas in the north (40) and the east (42) of the sea and a large coastal lagoon area of Kolyuchinskaya Guba (41).
42
*Calculated only for geographical boundaries of the seas. Area %: area as share of the area of a particular sea or two neighbouring seas; N CFs: number of most important and important CFs per area (min/max); AvN CFs: average number of most important and important CFs per area (SD). As several CPA cover parts of different seas, separate calculations were done for a particular seas and the neighbouring seas.
9 (6.01) 6–23 38 4086–33129 43,44,45,46,47 5 Bering
9 (3.85)
17 (5,95) 4–21 27 582–31048 38,39,40,41,42 5 Chukchi
10.5 (3.74) 7–18
7–18 11
16 1050–61057
1050–61057 34,35,36,37,38,39
29,30,32,33,34,35,36,37,38,39 10
6 East‐Siberian
Laptev and east‐Siberian
11 (3.07)
8 (4.47) 3–23
7–15 23
25 1027–83217
4190–55300 29,30,32,33,34
13,15,24,25,26,27,28,29,30,31,32,33,34 13
5 Laptev
Kara and Laptev
7.5 (5.95)
7 (4.98) 3–23
3–23 27
27 245–88920
1027–68416 13,15,24,25,26,27,28,29,30,31
1,2,3,4,5,12,13,14,15,16,17,18,19,20,21,22,23,24,25,26,27,28,29,30,31 25
10 Kara
Barents and Kara
10.5 (4.94)
7 (5.29) 3–23
6–21 33
27 245–88920
96–12377 5,6,7,8,9,10,11
1,2,3,4,5,12,13,14,15,16,17,18,19,20,21,22,23 17
7 White
Barents
Area IDs (Figure 9). Number of CPAs Sea
TABLE 4
Selected conservation priority areas (CPA) in particular seas and boundary areas*
Size range (km2)
Area %
N CFs
AvN CFs
SOLOVYEV
ET AL.
In the Russian part of the Bering Sea the entire western part of the Bering Strait was selected (43) along with the coastal zone of the southern Chukotka Peninsula including the region of Sireniki polynya (44). Other contrasting areas are the Anadyr Liman with estuarine conditions (47), extensive shelf area of the Gulf of Anadyr (45), and the Navarin Cape area (46) which includes various coastal lagoons and part of the Northern Bering Sea front.
6 | R EP RE S E N T A T I V E N E S S O F T H E S E L EC T E D N E T W O R K I N R E L A T I O N T O B I O GE O G R A P H I C A L U N I T S This was assessed using a regionalization system for benthic invertebrates (Petryashov et al., 2010, 2013; Spiridonov, 2011; Spiridonov et al., 2015) which is the most developed biogeographical regionalization scheme for the Eurasian Arctic (Table 5). Table 5 summarizes
the
representation
of
particular
biogeographical
regions in the network of conservation priority areas. All biogeographical units were represented in all relevant seas except the Amerasian Arctic province in the Chukchi Sea. That said, this province in the Chukchi Sea is located in the north and largely outside Russia's EEZ (Petryashov et al., 2013). Targets for representation of particular large biogeographical regions were not specified for particular seas but for the Russian Arctic in general. In spite of this, such large regions as the North Atlantic/Arctic transitional zone, Eurasian Artic Province and the Siberian Shelf province were represented by several large areas in all relevant seas (Table 5). Furthermore these areas capture distinct parts of respective biogeographical regions. For example the North Atlantic/Arctic transitional zone was represented by a series of coastal priority areas reflecting a gradient of species assemblages along the Murmansk coastal current direction (2–4), the western coast of Novaya Zemlya (16, 17, 19), the unique boreal refugium in the Chioshkaya Bay (21), and the bays of the White Sea with different conditions and associated fauna (6–11), along with offshore areas in different sections of the Polar Front (12, 18). The Siberian Shelf province is represented by transitional areas in the very south‐east of the Barents Sea, an enclave in the White Sea trough and areas with different levels of influence from estuarine waters in the Kara and the Laptev Seas. The Eurasian Arctic province was represented by the several areas in the north of the Barents and Kara Seas but could be underrepresented in the Laptev Sea (Table 5). Several areas cover the boundary zone between the Eurasian Arctic and the Siberian Shelf province (15, 30, 35). Finally, the transitional zone between the Arctic and North Pacific realms was represented by several areas in the Chukchi Sea and the refugium in Chaun Bay in the East Siberian Sea (36). Northern outposts of non‐Arctic biotas were selected in the south‐west of the Barents Sea (part of the Scandinavian province, 1), in the south of the Chukchi Sea (42) and in the north‐western Bering Sea (43–47).
6.1
|
Overlapping with existing protected areas
The total size of the existing protected areas is about 127 000 km2 or less than 3% of the total research area, thus they achieve conservation targets for only 36.4% of selected CFs (Table 5).
43
ET AL.
Bering
43–47
Results of the basic scenario of MARXAN analysis (Scenario 1, Figures 6, 7) show that the total area that needs to be protected to
32, 33, 34, 35 (part)
slightly bigger area – almost 793 000 km2 (17.2% of the Russian Arctic
42 (part)
39–41, 42 (part)
with existing PAs included (i.e. Scenario 2, Figure 6) demonstrate only a seas area) (Table 6). Most of the existing federal nature protected areas of the Russian Federation overlap with selected conservation priority areas
36 (part)*
(Figure 10). Overlapping is observed in the areas of the largest currently protected areas in the Russian Arctic seas: the Franz Josef Land area of the Russian Arctic National Park with area 13, and the Wrangel Island Zapovednik (strictly protected reserve) with area 39. The Kolyuchinskaya Guba (area 41) and parts of area 43. Some other important areas include small coastal zones of several federal reserves.
30 (part)
The total area of overlap of conservation priority areas with marine area of federal nature protected areas is 105 489 km2 or 83.05% of the total area of existing protected areas or 11% of conservation priority areas.
15 (part), 29, 30 (part)
24, 25, 31, 15 (part), 30 (part) 6–8, 10–11, 9 (part)
km2 or 16.7% of the Russian Arctic seas. Results of the basic scenario
recently established National Park Beringia includes most of the
26, 27, 28
Laptev Kara
7
|
DISCUSSION
7.1 | Comparison of the Russian Arctic case with other large‐scale systematic marine conservation planning efforts Systematic marine conservation planning is a relatively new field (Wells et al., 2016). However, there have been a few attempts to apply this approach to extensive marine areas, i.e. covering more than one sea or LME, which are comparable with the sector of the Arctic that
9 (part)
White
36 (part), 37, 38
35 (part)
36 (part)
E‐Sib
Chukchi
Not selected
achieve all the conservation targets should be no less than 772 000
Sea
the present study looks at. servation planning is rezoning of the Great Barrier Reef in Australia. In this project separate reefs were taken as planning units with buffer The most important CFs were 70 bioregions of particular types (both reef and non‐reef biotopes) derived from statistical modelling and 12 (part), 13, 14
expert analysis. The cost of a unit was a function of various human interests (i.e. fishing, recreation, use by indigenous people, and conservation) (Ball et al., 2009; Fernandes et al., 2005). *Chaun Bay refugium (Petryashov et al., 2010)
Transitional North Pacific/ Arctic zone
North Pacific realm
Conservation Law Foundation of USA (CLF) and WWF Canada ini-
Amerasian Arctic Province
Eurasian Arctic Province
23 Ob‐Yenissean Province
Siberian Shelf Province
5 (part), 12 (part), 18, 20
zones and the spaces between them divided into equal hexagons.
AATZ offshore
1
2–4, 5 (part), 16, 17, 19, 21, 22 (part) Atlantic/ Arctic transitional zone (AATZ) coastal
Scandinavian province
Barents
The classic example of how MARXAN can be used for marine con-
Biogeographical region
TABLE 5 Breakdown of selected areas of high conservation priority (as numbered in Figure 9) by major biogeographical regions (Petryashov et al., 2010, 2013; Spiridonov, 2011; Spiridonov et al., 2015) in particular seas. Grey: Non‐applicable
SOLOVYEV
tiated a project of systematic MPA planning of the Atlantic shelf of Canada. Although smaller in geographical extent this project had similar aims to the current study. The following groups of CF were used: areas of persistently high chlorophyll concentration obtained using Sea WIFS satellite images, demersal fish species richness in the bottom trawl surveys, adult and juvenile fish abundance, cetacean abundance, and habitat types classified from abiotic data, benthic and water characteristics (CLF/ WWF, 2006; Roff & Zacharias, 2011). The targets were set at 20% of high chlorophyll concentrations within the planned units, 20% of species richness or relative abundance contained in planned units at or above the mean for biogeographical area, and 20% of each seascape type. All planning units were assigned the same cost.
44
SOLOVYEV
TABLE 6
ET AL.
Parameters comparison of existing PAs in the Russian Arctic seas with the outputs of MARXAN analyses Total area, km2 (percentage of the total working area)
Conservation targets achieved (share of the total number of targets)
1. Basic: Normal targets, all CFs included into analysis
771 924 (16.73%)
195 (100%)
2. Basic + existing PAs included in the analysis
792 913 (17.19%)
195 (100%)
3. Only existing PAs included in the analysis
127 014 (2.75%)
71 (36.4%)
MARXAN scenarios
FIGURE 10
Overlapping of selected conservation priority areas with existing marine protected areas in the Russian Arctic
The largest marine region ever explored for conservation planning
(2015). Adding productivity characteristics would increase this number
using MARXAN prior to the current study was the North‐east Atlantic
by an order of magnitude. Statistical modelling and extensive expert
(the High Sea area outside the regional seas and EEZs of coastal states)
evaluation could reduce this number but for such a huge area as the
(Evans, Peckett, & Howell, 2015). This analysis used combinations (e.g.
Russian Arctic seas it would require an enormous amount of prelimi-
water masses plus seafloor kinds) of types of habitats and areas of high
nary work, much more than in the case of the Great Barrier Reef. In
physical diversity as a surrogate for biological diversity. The planning
addition, research would have to take into account a number of CFs
units were ICES statistical rectangles measuring 30 min latitude by 1
covering vertebrate populations not necessarily coinciding with biore-
degree longitude and thus the exact area in km2 varies with longitude.
gions as well as distinctive entities (such as VMEs).
The study by Evans et al. (2015) was mostly concentrated on achieving
Owing to time constraints and limited financial resources it was
efficient representation of habitat types and played therefore with dif-
decided to set aside this approach; however, it was noted that it was
ferent scenarios with varying conservation targets and BLM.
needed in order to perform a comprehensive assessment and deserved
All the above‐mentioned studies including the current one used
to be considered in the future. Instead, MARXAN was set to freely
very different approaches to the selection of habitat and conservation
combine particular habitat features even though they could be partly
features. The North‐east Atlantic and the Great Barrier Reef projects
overlapping (i.e. bathymetric zones, sediment classes and widespread
dealt with bioregionalization schemes. Unlike them, the study of the
types of benthic communities). This increased the likelihood of achiev-
Russian Arctic seas was not based on a single regionalization scheme.
ing appropriate representativeness of habitats through MARXAN runs,
A rough calculation of simple combinations for bioregions identified
one way or another.
on the basis of bathymetry, geomorphological characteristics of the
Similar to the CLF/WWF study (Roff & Zacharias, 2011) the pres-
coastline and seabed, sediments, water masses and fronts, sea ice
ent attempt at conservation planning was grounded upon both
regimes and biotic composition for macrophytes would result in a
representation of biogeographical regions and habitats and the
few hundred thousand bioregions of the scale comparable with the
distribution of life forms and distinctive areas. In contrast to the iden-
one used in the studies by Fernandes et al. (2005) and Evans et al.
tification of priority areas for conservation by CLF/WWF Canada the
SOLOVYEV
45
ET AL.
oceanographical characteristics were not directly integrated in the CF
intense commercial fishing (Bohanov, Lajus, Moiseev, & Sokolov, 2013;
set, except for prolonged MIZ and flaw polynyas which themselves
Lajus et al., 2005; Shevelev, Sunnanå, & Gusev, 2011) and there are arti-
may correspond to biological entities. Instead they influenced the costs
sanal and small‐scale commercial fisheries in the White Sea (Lajus et al.,
of planning units.
2005; Spiridonov & Suprunenko, 2016; Stasenkov et al., 2011) and
While the conservation planning for the Atlantic shelf of Canada
some coastal areas in the Kara Sea (Ulchenko et al., 2016) and marine
and New England used CFs reflecting pelagic productivity (i.e. areas
hunting and fishing in Chukotka (Bogoslovskaya, Slugin, Zagrebin, &
of high chlorophyll concentration) the study of the Russian Arctic did
Krupnik, 2007), there have been no fisheries in most of the Russian
not. The reason for this is the extremely high variability of primary pro-
Arctic and it is uncertain if any fishery development is possible in the
duction characteristics in the water column of the Arctic seas both spa-
region. The coastal regions of the western Kola Peninsula in the Barents
tially and seasonally (Vetrov & Romankevich, 2009, 2011) and the lack
Sea and the White Sea are experiencing a surge of tourism which is
of comparable data for alternative sources of primary production such
poorly regulated (Spiridonov & Suprunenko, 2016), while other poten-
as sea ice flora and microbiota (Carmack et al., 2006; Ilyash & Zhitina,
tially attractive areas remain generally pristine. Some of them are still
2009; Romankevich & Vetrov, 2001). However, the inclusion of
new to vessel‐based cruise tourism.
polynyas and marginal ice zone, known for their impact on primary
While active production of natural gas is underway in the Yamal
production (Carmack & Wassmann, 2006; Carmack et al., 2006), and
Peninsula and construction of terminals and pipelines is progressing
indirect effects of decreasing costs of planning units in oceanographi-
(WWF Russia, 2016), in most of the Russian Arctic seas hydrocarbon
cal fronts known for enhancing the effect on biological productivity
exploration remains limited. However, there are vast areas licensed
and biomass concentration (Carmack & Wassmann, 2006; Flint,
for hydrocarbon exploration (Amiragyan, 2016; Rosneft, 2016) and
Poyarkov, & Soloviev, 2015; Sakshaug, 2004; Sakshaug, Bjørge,
taking them into account would seriously bias conservation priorities.
Gulliksen, Loeng, & Mehlum, 1994) made it possible to account for
Considering the above‐mentioned it is currently impossible to esti-
essential productivity features (Spiridonov et al., 2017).
mate the costs associated with multiple present and, more impor-
The important difference of the Russian Arctic conservation plan-
tantly, potential economic activities for a particular unit. However,
ning experiment from others that are comparable in scale using
such costs should be considered during the next step when system-
MARXAN applications to marine conservation priority areas was that
atic conservation planning is done at a finer scale for particular seas
the latter either considered mostly the coastal zone (Ball et al., 2009;
and their subdivisions. This will require developing a set of new
Fernandes et al., 2005) or excluded it from the analysis (CLF/ WWF,
layers based on current economic activity (i.e. industrial fishery in
2006) while in this study both inshore and offshore planning units
the Barents Sea, shipping, natural gas extraction infrastructure in
were considered. This was necessary because of the enormous influ-
Yamal Peninsula, closed military areas, traditional coastal activities,
ence that coastal processes have on marine biodiversity in the Russian
and tourism), as well as modelled expected activities, such as hydro-
Arctic including formation of landfast ice, polynyas, and river discharge
carbon development, new shipping routes and possible industrial
(Spiridonov et al., 2011). In addition, many important vertebrate spe-
fishing beyond the Barents Sea.
cies such as seabirds, walruses, ring seals and beluga whales, and anadromous and semi‐anadromous fishes use both offshore and inshore/ estuarine habitats.
7.2
|
MARXAN and post‐MARXAN analysis
Separate analysis of inshore and offshore parts of the study area
Despite the fact that MARXAN is the only decision support tool in
would undermine connectivity of the resulting network of priority con-
most of the projects. The final outputs are considered to be poten-
servation areas and thus make very little sense. Moreover coastal and
tial protected areas, and the borders of potential MPAs usually
offshore habitat features and CFs should be analysed over different
match the borders of the areas selected by MARXAN. By contrast,
spatio‐temporal scales (Mokievsky, 2009; Roff & Zacharias, 2011)
the present survey attached special importance to post‐MARXAN
which would result in very uneven distribution of size of selected
analysis. Comparison of the final configuration and MARXAN pro-
areas, i.e. relatively small coastal areas in the Barents and White Seas
posed areas (basic scenario 1) is shown on the map (Figure 11)
vs a huge area along the outer shelf and slope of the Kara Sea
and in Table 7).
(Table 4; Figure 8). The studies for the Great Barrier Reef (Fernandes
There are some notable differences between the two configura-
et al., 2005), the Atlantic shelf of New England and Canada (CLF/
tions of the network. The experts increased the total size of the area
WWF, 2006) and the High Sea of the North‐east Atlantic (Evans
from 771 924 km2 (16.73%) to 1 145 117 km2 (24.8% of the Russian
et al., 2015) all selected areas that were comparable in size, however,
Arctic seas area). Overlap between MARXAN proposed areas and
this might be an initial intention of the authors.
areas in the final configuration chosen by experts is about 80% for
Although human use is a critical factor for systematic conservation
the areas most frequently selected by the algorithm and just a little
planning, the present study did not consider the increased costs of
above 70% for the areas with selection frequency of 60%. The experts
establishing a conservation regime in the areas of economic interest.
also included some areas that were not chosen by MARXAN and
This makes it very different from the rezoning of the Great Barrier Reef
ignored some of the MARXAN proposals.
(Ball et al., 2009), which, according to its rationale primarily focused on human uses. Economic activity in the Russian Arctic remains very uneven. While a significant part of the Barents Sea is among the world's oldest sites of
In total 11 new areas were proposed, 27 areas resulting from MARXAN analyses had their shape changed and enlarged, for two areas the size was reduced and two areas proposed by MARXAN were excluded by the experts (Figure 11).
46
SOLOVYEV
FIGURE 11
TABLE 7
ET AL.
Comparison of the network of conservation priority areas proposed by experts with the outputs of MARXAN analysis
Comparison of the final configuration of the CPAs network and MARXAN proposed areas (basic scenario 1) Total size of the areas proposed by MARXAN, thousands km2
Total size of intersection of conservation priorities areas, thousands km2
Share from the total area, proposed by MARXAN, %
Selection frequency 60%
663.1
502.5
71.4
Selection frequency 80%
483.8
378.9
78.3
Selection frequency 95%
304.9
243.8
79.9
Best selection
789.0
547.1
69.3
PU
For example, Victoria Island (area 14) and the Chioshskaya Guba
Some enlargements such as the area to the north of Franz Josef
(21) in the Barents Sea, Zhelania Cape to the north of Novaya Zemlya
Land waters (area 13), or new areas like area 14 (Victoria Island waters)
archipelago (15), areas to the north of Novosibirskie Islands (34, 35),
weren't selected originally by MARXAN and were added by the expert
and the area around Navarin Cape (46) in the Bering Sea weren't pre-
team during post‐MARXAN analysis because of gaps in the data used
sented on the selection frequency map after the final MARXAN runs;
for the MARXAN analysis, that did not show specificity and unique-
these as well as some other areas were proposed by experts and
ness of these particular areas for the developing network. This was
subsequently recognized as areas of conservation priority.
the second commonest reason for correction of areas established by
Some areas were enlarged significantly: in the area to the north of the Franz Josef Land archipelago (13), the Baydaratskaya Bay (24), the
MARXAN analysis. There were seven cases where existing areas were corrected or new areas proposed for this reason.
Gorlo (6), and the area to the north of Chukchi Peninsula (42). For
In two cases experts decided to select different parts of areas than
some areas boundaries were partly changed, e.g. for the water around
were proposed by MARXAN. For instance, in the Laptev Sea an area of
Wrangel Island (39) and the area of the Lena River delta (33). Some
the Great Siberian Polynya to the north of Novosibirskie Islands (34,
areas chosen by MARXAN weren't included in the final network, the
35) was selected because its diversity and productivity was higher than
most significant was a large area in the Laptev Sea between Taymyr
in the central part of the Polynya as chosen by MARXAN, based on the
Peninsula and the Lena River delta.
criterion of representativeness for some of the communities on a
The changes to the boundaries of 23 areas (enlargements or partial changes of boundaries) were made because the areas defined by
particular benthic substrate, because that criterion was already met in other selected areas.
experts followed contour lines along isobaths or other natural bound-
Some areas were altered or added for sustainability reasons – for
aries. It is customary in Russia to define boundaries of protected areas
example, the Chioshskaya Bay (21) was added to the network partly
following natural lines instead of using regular geometric shapes as
because it, along with benthic communities representativeness, pro-
many countries do.
vides alternative grounds for moulting harp seals in the years when
SOLOVYEV
47
ET AL.
ice conditions in the White Sea are unsuitable (Svetochev, 2013).
one or two orders of magnitude and many are 103–104 km2 in size,
Others, like the areas to the south of the Bering Strait (44) along the
i.e. a minimal biogeographical unit (Mokievsky, 2009) or an ecoregion
shores of the Chukchi Peninsula between two patches proposed by
(Roff & Zacharias, 2011).
MARXAN, were selected for reasons of connectivity (Solovyev,
Roff and Zacharias (2011) define an ecoregion as an area of rela-
Zagrebin, Glazov, Litovka, & Kosyak, 2013). There are seven areas
tively homogenous species composition, which is likely determined
where original boundaries were changed for reasons of sustainability,
by the predominance of a distinct suite of oceanographical or topo-
representativeness and connectivity.
graphic features. Indeed, most priority areas are based on such fea-
All these changes made by experts were only possible due to the
tures (Spiridonov et al., 2017), although most of them with the
transparency of the MARXAN‐based approach to analysis. All inputs,
exception of polynyas were not included in MARXAN analysis. The
changes and corrections were documented which allowed external
proposed network of conservation priority areas in the Russian Arctic
experts who were invited at later stages to participate in a broader
seas would consist of seascape‐ to ecoregion‐scale units which repre-
team to analyse results and understand how different parameters
sent practically all currently defined biogeographical provinces
and data influenced the outcomes of specific runs.
(Table 5) and would include different types of bays and straits
MARXAN proved to be a very convenient decision support tool
(although apparently not all the types) and most archipelago areas.
instrumental for structuring data and the process of analyses, but
Further research and analysis on CFs might reveal that other parts
serious post‐MARXAN analysis is required to interpret and correct
of the region also deserve the status of conservation priority areas.
the outputs.
However, we believe that they would be relatively small, probably not exceeding 103 km2. Even large conservation priority areas in the Arctic are used by highly migratory species of fish, seabirds and marine
8
|
T HE P R O P O S E D N E T W O R K
mammals only for short periods during the year. Their prey, such as polar cod is not confined to the conservation priority areas either.
The existing set of federal specially protected areas in the Russian
Therefore analysing the level of connectivity (Roff & Zacharias,
Arctic seas was shaped by the history of their development, while
2011) of the network with particular reference to highly migratory
long‐term planning and analysis of the challenges of preserving
top predators, many of them being iconic species for the Arctic, is a
marine biological diversity played little significant role in their
separate task. The authors intend to conduct a further special study
formation (Spiridonov et al., 2012). However, more than 80% of
of this subject.
existing protected areas were selected on the basis of MARXAN
Another critical issue is the sustainability of the suggested net-
analysis. This indicates close association of the priority conserva-
work in the face of the changing climate. There are several scenarios
tion features on the coast (which primarily determined the estab-
of how ecosystems might change under the influence of the current
lishment of the existing protected areas) with conservation
trends, such as the increasing input of the Atlantic and Pacific waters
features at sea.
into the Arctic, decreasing summer sea ice cover, change in the propor-
It should also be noted that in recent years a number of large
tion of multi‐year ice and increasing average temperature (Alexander
protected areas were established around the protected areas on the
et al., 2013; Carmack et al., 2006; Fossheim et al., 2015; Hunt et al.,
Franz Josef Land and Wrangel Island which significantly increased
2016; Kedra et al., 2015; Laidre et al., 2015; Melnikov, 2008).
the size of area under protection (Spiridonov et al., 2012). However,
A possible way to account for these changes could be continuous
the present study shows that a large marine area containing numerous
modelling for all the CFs based on the changing factors and repeated
important CFs as well as a number of biogeographical regions in the
MARXAN analysis of all possible scenarios. This would be a very
Russian Arctic remains outside the federal system of protected areas
resource‐intensive and time‐consuming exercise but an extremely
and according to the Ministry of Natural Resources and Environment
important one since biodiversity indicators in most of the selected
of the Russian Federation the existing plans to establish new PAs in
areas are based on particular oceanographical and other environmental
the region do not address these concerns.
features (Spiridonov et al., 2017). Possible climate‐related changes of
The network of conservation priority areas proposed by the
underlying environmental features of the proposed priority areas could
present project would provide protection for large parts of Arctic seas.
also be discussed and explored. We therefore consider the proposed
Large areas covering 25–30% of all seas with the exception of the East
network to present a sound basis for future development of the
Siberian Sea (Table 3) were identified as conservation priority areas.
protected areas and marine spatial planning in the Arctic.
This proportion does not depend on the size of the area under analysis, but there is a certain correlation between the size of specific proposed areas and the size of the marine basins in which they are located (i.e. smallest area is located in the White Sea and the two largest are in the Barents Sea and the Kara Sea).
9 | C O NC L U S I O NS : L E S S O N S F R O M TH E P R E S E NT SY S T E M A T I C C O N S E R V A T I O N PL AN NI NG R E SE ARC H
Mokievsky (2009) discussed the spatial scales that are sufficient to protect various habitat and conservation features in the World Ocean. 2
2
The first attempt to apply systematic conservation planning to the
He considered the scale of 10–10 km to be appropriate for the
selection of protected areas in the Russian Arctic seas revealed that
protection of series of benthic communities or seascapes. Most of
the available data for this vast area comprising about one‐third of the
the priority areas identified in the present study exceed this size by
Arctic Ocean were unevenly distributed and highly heterogenous
48
SOLOVYEV
(Figure 2; Table S1). However, even these data were sufficient to identify, through a series of experts' consultations, a set of conservation features (CFs) that met the EBSA criteria. Thus the present dataset includes a list of representative and distinctive areas which could be modified as and when more comprehensive data are available. The present study presents an alternative approach to how MARXAN could be used as a decision support tool. In contrast with other large‐scale studies that applied an integrated habitat classification the present research used several independent habitat classifications in various combinations. Another difference is that oceanographical features such as water masses and fronts were used, not to define integral bioregions and CFs, but to adjust the cost of a unit, i.e. to reduce the cost for units corresponding to frontal systems. The primary lesson learnt from the present study is that the optimal way to use MARXAN as a decision support tool is to supplement software runs with repeated expert analysis of results and post‐ MARXAN analysis. This iterative procedure and post‐MARXAN analysis did not radically change the MARXAN‐proposed network but allowed the identification of a more balanced system of conservation priority areas spread rather evenly throughout the Russian Arctic seas (covering from 25 to 30% of the sea area). The system encompassed both offshore and coastal zones ranging from relatively small shallow coastal lagoons and fjords with distinct features to extensive areas covering various biotopes in the shelf and upper slope zones. The resilience of the resulting network to climate‐induced ecosystem changes and potential surge of economic activity in the region deserves further examination; so does the institutional basis for its implementation (i.e. as specially protected areas in a strict sense, marine spatial planning zones, fishery management areas, etc.). We believe that the suggested approach combining MARXAN and post‐MARXAN analysis and the resulting network could become the first step towards systematic planning of the marine priority conservation areas in the pan‐Arctic region. ACKNOWLEDGEMEN TS This project was initiated by WWF Russia and funded by Oceans 5 foundation, WWF Netherlands and WWF Russia. The authors would like to thank all experts participating in national and international meetings for their comments, review and ideas for this research. Without their input this project would not have been possible. The authors thank Olga Movsinskaya for her assistance in manuscript preparation and John Roff, Jan Ekebom and the third anonymous reviewer, and John Baxter the editor of the journal for their careful review that
ET AL.
(Eds.), Contribution of working group I to the fifth assessment report of the intergovernmental panel on climate change (pp. 3–30). Cambridge, UK: Cambridge University Press. AMAP/CAFF/SDWG. (2013). Institute of Marine Research (IMR). Bergen http://wwfarcticmaps.org/ Accessed on 25 December 2016 Amiragyan, A. (2016). Oil and gas in Russian Arctic. TEC v Rossii, 09, 35–39. (in Russian) Amstrup, S. C., Marcot, B. G., & Douglas, D. C. (2008). A Bayesian network modeling approach to forecasting the 21st century worldwide status of polar bears. In Arctic sea ice decline: Observations, projections, mechanisms, and implications (pp. 213–268). Ardron, J. A., Possingham, H. P., & Klein, C. J. (Eds) (2010). MARXAN good practices handbook, Version 2. Victoria, BC, Canada: Pacific Marine Analysis and Research Association. www.pacmara.org Ball, I. R., & Possingham, H. P. (2000). MARXAN (V1. 8.2). Marine reserve design using spatially explicit annealing, a manual. Ball, I. R., Possingham, H. P., & Watts, M. (2009). MARXAN and relatives: Software for spatial conservation prioritisation. In A. Moilanen, K. A. Wilson, & H. P. Possingham (Eds.), Spatial conservation prioritisation: Quantitative methods and computational tools (pp. 185–195). Oxford, UK: Oxford University Press. Bauch, D., Dmitrenko, I., Kirillov, S., Wegner, C., Hölemann, J., Pivovarov, S., … Kassens, H. (2009). Eurasian Arctic shelf hydrography: Exchange and residence time of southern Laptev Sea waters. Continental Shelf Research, 29, 1815–1820. Bauch, D., Dmitrenko, I. A., Wegner, C., Hölemann, J., Kirillov, S. A., Timokhov, L. A., & Kassens, H. (2009). Exchange of Laptev Sea and Arctic halocline waters in response to atmospheric forcing. Journal of Geophysical Research, 114. C05008. https://doi.org/10.1029/2008JC005062 Bivand, R., Keitt, T., & Rowlingson, B. (2016). Rgdal: Bindings for the Geospatial data Abstraction library. R package version, 1, 2–4. https:// CRAN.R‐project.org/package=rgdal Bogoslovskaya, L., Slugin, I., Zagrebin, I., & Krupnik, I. (2007). Basis of marine mammal hunting. Moscow: Heritage Institute. (In Russian) Bohanov, D. V., Lajus, D. L., Moiseev, A. R., & Sokolov, K. M. (2013). Assessemment of threats to the Arctic marine ecosystem associated with commercial fishery: The Barents Sea case. Moscow: WWF Russia. (in Russian) Boyer, T. P., Baranova, O. K., Biddle, M., Johnson, D. R., Mishonov, A. V., Paver, C., … Zweng, M. (2012). Arctic regional climatology. Regional Climatology Team, NOAA/NODC www.nodc.noaa.gov/OC5/regional_ climate/arctic Carmack, E., Barber, D., Chistensen, J., Macdonald, R., Rudels, B., & Sakshaug, E. (2006). Climate variability and physical forcing of the food webs and the carbon budget on panarctic shelves. Progress in Oceanography, 71, 145–181. Carmack, E., & Wassmann, P. (2006). Food webs and physical–biological coupling on pan‐Arctic shelves: Unifying concepts and comprehensive perspectives. Progress in Oceanography, 71, 466–477.
helped to improve the manuscript significantly.
CBD. (2010). Convention on Biological Diversity. http://cbd.int/sp/targets/ Accessed on 24 December 2016.
DIS CLOSURE/CONF LICT OF INTERES T
Chernova, N. V. (2011). Distribution patterns and chorological analysis of fish fauna of the Arctic region. Journal of Ichthyology, 51, 825–924.
The authors declare no conflicts of interest. ORCID Boris Solovyev
http://orcid.org/0000-0002-8328-8040
RE FE R ENC E S Alexander, L. V., Allen, S. K., Bindoff, N. L., Breon, F. M., Church, J. A., Cubasch, U., … Gregory, J. M. (2013). Summary for policymakers, climate change 2013: The physical science basis. In T. F. Stocker, D. Qin, G.‐K. Plattner, M. M. B. Tignor, S. K. Allen, J. Boschung, et al.
CLF/ WWF. (2006). Marine ecosystem conservation for New England and maritime Canada: A science‐based approach to identifying priority areas for conservation. In Boston, USA: Conservation Law Foundation. Halifax, Canada: WWF Canada. Denisenko, S. G., Sirenko, B. I., Gagaev, S. Y., & Petryashov, V. V. (2010). Bottom communities: Structure and spatial distribution in the east Siberian Sea at depth more than 10 m. In B. I. Sirenko, & S. G. Denisenko (Eds.), Fauna of the East Siberian Sea: Distribution patterns and structure of bottom communities (Explorations of the Fauna of the seas, vol. 66 (74)) (pp. 130–143). St. Petersburg: Zoological Institute of the Russian Academy of Sciences. (in Russian)
SOLOVYEV
ET AL.
Dmitrenko, I. A., Polyakov, I. V., Kirillov, S. A., Timokhov, L. A., Simmons, H. L., Ivanov, V. V., & Walsh, D. (2006). Seasonal variability of Atlantic water on the continental slope of the Laptev Sea during 2002–2004. Earth and Planetary Science Letters, 244, 735–743. Dobrovolsky, A. D., & Zalogin, B. S. (1982). Seas of USSR. Moscow: Moscow University Press. (In Russian) Dobrynin, D. (2015). Ice habitats. Technical report. Moscow: WWF Russia (in Russian). ESRI. (2006). ArcGIS Desktop: Release 9.2. Redlands, CA: Environmental Systems Research Institute. Evans, J. L., Peckett, F., & Howell, K. L. (2015). Combined application of biophysical habitat mapping and systematic conservation planning to assess efficiency and representativeness of the existing high seas MPA network in the Northeast Atlantic. ICES Journal of Marine Science, 72, 1483–1497. FAO. (2009). International guidelines for the management of deep‐sea fisheries in the High Seas. Rome: FAO. Fernandes, L., Day, J. C., Lewis, A., Slegers, S., Kerrigan, B., Breen, D., … Stapleton, K. (2005). Establishing representative no‐take areas in the Great Barrier reef: Large‐scale implementation of theory on marine protected areas. Conservation Biology, 19, 1733–1744. Flerov, B. K. (1932). Distribution of algae of the Novaya Zemlya coasts. Trudy GOIN, 2(1), 1–45. (in Russian) Flint, M. V., Poyarkov, S. G., & Soloviev, K. A. (2015). Mesoplankton of the continental slope area in the Kara Sea. In M. V. Flint (Ed.), Ecosystem of the Kara Sea – new data of expedition research (pp. 129–134). Moscow: P.P. Shirshov Institute of Oceanology. ISBN: 978‐5904761‐49‐3. (in Russian) Fossheim, M., Primicerio, R., Johannesen, E., Ingvaldsen, R. B., Aschan, M. M., & Dolgov, A. V. (2015). Recent warming leads to a rapid borealization of fish communities in the Arctic. Nature Climate Change, 5, 673–677. Frolov, I. E., Gudkovich, Z. M., Karklin, V. P., Kovalev, E. G., & Smolyanitsky, V. M. (2009). Climate change in Eurasian Arctic shelf seas. Chichester, UK: Praxis Publishing. Gavrilo, M. V., & Spiridonov, V. A. (2011). Sea ice habitats and associated ecosystem. In Spiridonov, V., Gavrilo, M., Nikolaeva, N., & Krasnova E. (Eds.) Atlas of the marine and coastal biodiversity of the Russian Arctic (pp. 25–26). Moscow, WWF Russia Publication. GDAL. (2016). GDAL ‐ Geospatial Data Abstraction Library: Version 2.1.2, Open Source Geospatial Foundation, http://gdal.osgeo.org Huettmann, F. (Ed.). (2012). Protection of the three poles. Tokyo, Japan: Springer. Hunt, G. L., Drinkwater, K. F., Arrigo, K., Berge, J., Daly, K. L., Danielson, S., … Laidre, K. (2016). Advection in polar and sub‐polar environments: Impacts on high latitude marine ecosystems. Progress in Oceanography, 149, 40–81. Ilyash, L. V., & Zhitina, L. S. (2009). Comparative analysis of species composition of sea ice diatoms of the Russian Arctic seas. Zhurnal Obschei Biologii, 70, 143–154. (In Russian) IUCN. (2007). Establishing networks of marine protected areas: making it happen – a guide for developing national and regional capacity for building MPA networks. cmsdata.iucn.org/downloads/nsmail.pdf, Accessed on 25 December 2016
49
Kiyko, O. A., & Pogrebov, V. B. (1997). Long‐term benthic population changes (1920‐1930 – Present) in the Barents and Kara seas. Marine Pollution Bulletin, 35, 322–332. Kudersky, L. A. (2004). Work on the acclimatization of pink salmon Oncorhynchus gorbuscha (Walbaum) in Russia. In Study, rational use and protection of resources of the Whites Sea. Proceedings of the IX International Conference. Petrozavodsk, 11–14 October 2004 (pp. 172–183)’ Petrozavodsk: Karelian Science Centre of Russian Academy of Sciences Publication (in Russian). Kupetsky, V. N. (1961). On seascapes of the Arctic. Proceedings of All‐Union Geographical Society, 93(4), 304–311. (in Russian) Laidre, K. L., Stern, H., Kovacs, K. M., Lowry, L., Moore, S. E., Regehr, E. V., … Born, E. W. (2015). Arctic marine mammal population status, sea ice habitat loss, and conservation recommendations for the 21st century. Conservation Biology, 29, 724–737. Lajus, D. L., Dmitrieva, Z. V., Kraikovski, A. V., Lajus, J. A., Yurchenko, A. Y., & Alexandrov, D. A. (2005). The use of historical catch data to trace the influence of cimate on fish populations: Examples from the White and the Barents Sea fisheries in 17th–18th centuries. ICES Journal of Marine Science, 62, 1426–1435. Loeng, H. (1991). Features of the physical oceanographic conditions of the Barents Sea. Polar Research, 10, 5–18. Margules, C. R., & Pressey, R. L. (2000). Systematic conservation planning. Nature, 405, 243–253. Margules, C. R., Pressey, R. L., & Williams, P. H. (2002). Representing biodiversity: Data and procedures for identifying priority areas for conservation. Journal of Biosciences, 27, 309–326. Maslanik, J., Stroeve, J., Fowler, C., & Emery, W. (2011). Distribution and trends in Arctic sea ice age through spring 2011. Geophysical Research Letters, 38. L13502. https://doi.org/10.1029/2011GL047735 Melnikov, I. A. (2008). Recent Arctic sea ice ecosystem: Dynamics and forecast. Doklady Earth Sciences, 423A, 1516–1519. Mokievsky, V. O. (2009). Marine protected areas: Theoretical background for design and operation. Russian Journal of Marine Biology, 35, 504–514. Moore, S. E., & Huntington, H. P. (2008). Arctic marine mammals and climate change: Impacts and resilience. Ecological Applications: a Publication of the Ecological Society of America, 18(2 Suppl), s157–s165. Naumov, A. D. (2001). Benthos. In V. Y. Berger, & S. Dahle (Eds.), White Sea. Ecology and environment (pp. 42–54). St.Petersburg – Tromsø: Derzhavets Publisher. PAME. (2015). Framework for a pan‐Arctic network of marine protected areas. Akureyri: PAME International Secretariat. Pantyulin, A. N. (2012). The features of the White Sea physics: Dynamics, structure and water masses. In A. P. Lisitsyn, & I. A. Nemirovskaya (Eds.), The White Sea system. Volume 2. Water column and its interaction with atmosphere, cryosphere, the river runoff, and biosphere (pp. 309–378). Moscow: Nauchnyi Mir. (in Russian) Pantyulin, A. N., & Chuprina, E. V. (2015). Development of methodology for pelagic regionalization as a basis for network of conservation priority areas within Russia's EEZ and the international waters of the Arctic Ocean. Technical report. Moscow: WWF Russia (in Russian).
Jeffries, M. O. Richter‐Menge J., & Overland J. E. (Eds.). (2015). Arctic Report Card 2015, http://www.arctic.noaa.gov/reportcard
Pavlov, V. A., & Sundet, J. H. (2011). Snow crab. In T. Jakobsen & V. K. Ozhigin (Eds.), The Barents Sea ecosystem, resources, management. Half a century of Russian‐Norvegian cooperation (pp. 168–172). Trondheim: Tapir Academic Press.
Jørgensen, L. L., Archambault, P., Armstrong, C., Dolgov, A. V., Edinger, E., Gaston, T., … Vecchione, M. (2016). Arctic Ocean. Arctic Ocean in The First Global Integrated Marine Assessment ‐ World Ocean Assessment I, 1‐47.
Petryashov, V. V., Vassilenko, S. V., Voronkov, A. Y., Sirenko, B. I., Smirnov, A. V., & Smirnov, I. S. (2013). Biogeographic analysis of the Chukchi Sea and adjacent waters based on fauna of some macrobenthic taxa. Invertebrate Zoology, 10, 49–68.
Kedra, M., Moritz, C., Choy, E. S., David, C., Degen, R., Duerksen, S., … Weslawski, J. M. (2015). Status and trends in the structure of Arctic benthic food webs. Polar Research, 34. 23775 doi.Org/10.3402/polar. v34.23775
Petryashov, V. V., Voronkov, A. Y., Vassilenko, S. V., Sirenko, B. I., Smirnov, A. V., & Smirnov, I. S. (2010). Biogeographical analysis of macrobenthos fauna in the East Siberian Sea and reconstruction of the fauna forming ways. In B. I. Sirenko, & S. G. Denisenko (Eds.), Fauna of the East Siberian
50
SOLOVYEV
Sea: Distribution patterns and structure of bottom communities (Explorations of the Fauna of the Seas, vol. 66 (74)) (pp. 160–177). St. Petersburg: Zoological Institute of the Russian Academy of Sciences (in Russian). Popov, A. V., & Gavrilo, M. V. (2011). Flaw polynyas. In V. A. Spiridonov, M. V. Gavrilo, N. G. Nikolaeva, & E. D. Krasnova (Eds.), Atlas of the marine and coastal biodiversity of the Russian Arctic (pp. 28–29). Moscow: WWF Russia. Quantum GIS Development Team. (2014). Quantum GIS Geographic Information System. Open Source Geospatial Foundation Project. http://qgis.osgeo.org R Core Team. (2016). R: A language and environment for statistical computing. Vienna, Austria: R Foundation for Statistical Computing. https://www. R‐project.org/ Roff, J., & Zacharias M. (2011). Marine conservation ecology. London: Earthscan Ltd. Roff, J. C. (2005). Conservation of marine biodiversity: Too much diversity, too little co‐operation. Aquatic Conservation: Marine and Freshwater Ecosystems, 15, 1–5. Romankevich, E. G., & Vetrov, A. A. (2001). Carbon cycle in the Arctic seas of Russia. Moscow: Nauka. (in Russian) Rosneft. (2016) Projects on shelf, https://www.rosneft.ru/business/ Upstream/offshore/#a1 Accessed on 24 December 2016 Rudels, B. (2015). Arctic Ocean circulation, processes and water masses: A description of observations and ideas with focus on the period prior to the international polar year 2007–2009. Progress in Oceanography, 132, 22–67. Sakshaug, E. (2004). Primary and secondary production in the Arctic seas. In R. Stein, & R. W. Macdonald (Eds.), The organic carbon cycle in the Arctic Ocean (pp. 57–81). New York, NY: Springer. Sakshaug, E., Bjørge, A., Gulliksen, B., Loeng, H., & Mehlum, F. (1994). Structure, biomass distribution, and energetics of the pelagic ecosystem in the Barents Sea: A synopsis. Polar Biology, 14, 405–411. Seidov, D., Antonov, J. I., Arzayus, K. M., Baranova, O. K., Biddle, M., Boyer, T. P., … Zweng, M. M. (2015). Oceanography North of 600N from World Ocean Database, 153–173. Shevelev, M. S., Sunnanå, K., & Gusev, E. V. (2011). History of fisheries and hunting. In T. Jakobsen & V. K. Ozhigin (Eds.), The Barents Sea ecosystem, resources, management: Half a century of Russian‐Norwegian cooperation (pp. 494–514). Trondheim: Tapir Academic Publishing. Skjoldal, H. R., & Toropova, C. (2010). Criteria for identifying ecologically important and vulnerable marine areas in the Arctic. Background document prepared for AMSA IIC and the IUCN ‘EBSA workshop’ in San Diego, November 2010, Society, 93, 304–311 (In Russian). Solovyev, B., Zagrebin, I., Glazov, D., Litovka, D., & Kosyak, A. (2013). Results of the beluga whale (Delphinapterus leucas) coastal observations along Chukchi penninsula in 1999‐2012. Izvestia TINRO, 174, 149–157. (in Russian) Spalding, M. D., Fox, H. E., Allen, G. R., Davidson, N., Ferdaña, Z. A., Finlayson, M. A. X., … Martin, K. D. (2007). Marine ecoregions of the world: A bioregionalization of coastal and shelf areas. Bio Science, 57, 573–583. Spiridonov, V., Gavrilo, M., Krasnov, Y., Makarov, A., Nikolaeva, N., Popov, A., … Krasnova, E. (2012). Towards the new role of marine and coastal protected areas in the Arctic: The Russian case. In F. Huettmann (Ed.), Protection of three poles (pp. 171–202). Tokyo, Japan: Springer. Spiridonov, V., Solovyev, B., Chuprina, E., Pantyulin, A., Sazonv, A., Nedospasov, A., … Onufrenya, I. (2017). Importance of oceanographical background for a conservation priority areas network planned using MARXAN decision support tool in the Russian Arctic seas. Aquatic Conservation: Marine and Freshwater Ecosystems, 27(Suppl. 1), 52–64. Spiridonov, V., & Suprunenko, Y. (2016). Traditional nature use of Pomors as a factor of conservation of the White Sea cultural landscape. In I. Krupnik (Ed.), Facing to the sea. In memoriam Ludmila Bogoslovskaya
ET AL.
(pp. 317–343). Heritage Institute: Moscow. ISBN: 978‐5‐600‐01365‐ 0. (in Russian) Spiridonov, V., Vedenin, A., Redkozubov, A., & Petryashov, V. (2015). A generalized biogeographical regionalization scheme for the Russian Arctic based on marine macrozoobenthos. Technical report to WWF Russia (in Russian). Spiridonov, V. A. (2011). Biogeographical regionalization. In V. A. Spiridonov, M. V. Gavrilo, N. G. Nikolaeva, & E. D. Krasnova (Eds.), Atlas of the marine and coastal biodiversity of the Russian Arctic (pp. 16–17). Moscow: WWF Russia. Spiridonov, V. A., Gavrilo, M. V., Krasnova, E. D., & Nikolaeva, N. G. (Eds) (2011). Atlas of marine and coastal biological diversity of the Russian Arctic. Moscow: WWF Russia. Spiridonov, V. A., & Zalota, A. K. (2017). Understanding and forecasting dispersal of non‐indigenous marine decapods (Crustacea: Decapoda) in east European and north Asian waters. Journal of Marine Biological Association of UK, 97(3), 591–611. https://doi.org/10.1017/ S0025315417000169 Stasenkov, V. A., Studenov, I. A., Novoselov, A. P., Kozmin, A. K., Pronina, O. A., Semushin, A. V., … Pastukhov, S. B. (2011). Pomor fisheries. Arkhangel: Northern Branch of PINRO. (in Russian) Strategy and Executive Plan for the Conservation of Biodiversity within the Russian Federation. (2014). Moscow. https://www.cbd.int/doc/world/ ru/ru‐nbsap‐v2‐en.pdf Svetochev, V. (2013). Biology and ecology of harp seal (Phoca groenlandica Erxleben, 1777) of White Sea population during first year of life. PhD thesis abstract. Murmansk. (in Russian) Trenberth, K. E., Jones, P. D., Ambenje, P., Bojariu, R., Easterling, D., Klein Tank, A., … Wuertz, D. (2007). Observations: Surface and Atmospheric Climate Change. In IPCC Fourth Assessment Report: Climate Change 2007. Working Group I: The Physical Science Basis (pp. 235–336). Cambridge: Cambridge University Press. https://archive-ouverte. unige.ch/unige:18698 Ulchenko, V. A., Matkovsky, A. K., Stepanov, S. I., Kochetkov, P. A., Yankova, N. V., & Gadinov, A. N. (2016). Fish resources and their use in the estuaries of the Kara and the Laptev seas. Trudy VNIRO, 160, 116–132. (in Russian) UNEP/CBD/COP/DEC/IX/20. (2008). Decision adopted by the conference of the parties to the convention on biological diversity at its ninth meeting. Conference of the parties to the convention on biological diversity, Annex I, Bonn, 19–30 May 2008, pp.7–10. UNEP/CBD/EBSA/WS/2014/1/5. (2014). Report of the Arctic regional workshop to facilitate the description of ecologically and biologically significant marine areas (Helsinki, 3–7 March 2014). https://www.cbd. int/doc/meetings/mar/ebsaws‐2014‐01/official/ebsaws‐2014‐01‐05‐ en.pdf Vetrov, A. A., & Romankevich, E. G. (2009). Production of phytoplankton in the Arctic seas and its response on recent warming. In Nihoul, J. C. J., & Kostianoi, A. G. (Eds.), Influence of climate change on the changing Arctic and sub‐Arctic conditions (pp. 95‐108). NATO science for peace and security series, 2009. https://doi.org/10.1007/978‐1‐4020‐9460‐6_8. Vetrov, A. A., & Romankevich, E. V. (2011). Primary production and fluxes of organic carbon to the seabed in the Russian Arctic seas as a response to the recent warming. Oceanology, 51, 266–277. Wells, S., Ray, G. C., Gjerde, K. M., White, A. T., Muthiga, N., Bezauy Creel, J. E., … Reti, J. (2016). Building the future of MPAs – Lessons from history. Aquatic Conservation: Marine and Freshwater Ecosystems, 26(Suppl. 2), 101–125. Wenzel, L., Gilbert, N., Goldsworthy, L., Tesar, C., McConnell, M., & Okter, M. (2016). Polar opposites? Marine conservation tools and experiences in the changing Arctic and Antarctic. Aquatic Conservation: Marine and Freshwater Ecosystems, 26(Suppl. 2), 61–84. WWF Russia. (2016). Yamal‐LNA. http://wwf.ru/about/what_we_do/oil/ full_list/yamalspg
SOLOVYEV
51
ET AL.
Zakharov, V. F. (1966). The role of flaw leads off the edge of fast ice in the hydrochemical and ice regime of the Laptev Sea. Okeanologiya, 6, 168–179. (in Russian) Zakharov, V. F. (1996). Sea ice in climate system. St. Petersburg: Gidrometeoizdat. (In Russian) Zalogin, B. S., & Kosarev, A. N. (1999). The seas. Moscow: Mysl. (in Russian)
and temperate waters of the World Ocean (Abstracts of presentations) (pp. 12–13). Leningrad: Nauka. (in Russian)
SUPPOR TI NG INF ORMATI ON Additional Supporting Information may be found online in the supporting information tab for this article.
Zatsepin, A. G., Kremenetskiy, V. V., Kubryakov, A. A., Stanichny, S. V., & Soloviev, D. M. (2015). Propagation and transformation of waters of the surface desalinated layer in the Kara Sea. Oceanology, 55, 450–460. Zatsepin, A. G., Poyarkov, S. G., Kremenetskiy, V. V., Nedospasov, A., Shchuka, S. A., Baranov, V. I., … Korzh, A. O. (2015). Hydrophysical features of deep water troughs in the western Kara Sea. Oceanology, 55, 472–484.
How to cite this article: Solovyev B, Spiridonov V, Onufrenya I, et al. Identifying network of priority areas for conservation in the Arctic seas: Practical lessons from Russia. Aquatic Conserv: Mar Freshw Ecosyst. 2017;27(S1):30–51. https://doi.org/
Zinova, A. D. (1974). Composition and phytogeographical division of the Arctic algal flora. In Hydrobiology and biogeography of shelfs in cold
10.1002/aqc.2806