BSEP116B Biodiversity in the Baltic Sea - Helcom
BSEP116B Biodiversity in the Baltic Sea - Helcom
BSEP116B Biodiversity in the Baltic Sea - Helcom
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144<br />
>30 psu<br />
18-30 psu<br />
11-18 psu<br />
7.5-11 psu<br />
5-7.5 psu<br />
0-5 psu<br />
>30 psu<br />
18-30 psu<br />
11-18 psu<br />
7.5-11 psu<br />
5-7.5 psu<br />
0-5 psu<br />
>30 psu<br />
18-30 psu<br />
11-18 psu<br />
7.5-11 psu<br />
5-7.5 psu<br />
0-5 psu<br />
>30 psu<br />
18-30 psu<br />
11-18 psu<br />
7.5-11 psu<br />
5-7.5 psu<br />
0-5 psu<br />
>30 psu<br />
18-30 psu<br />
11-18 psu<br />
7.5-11 psu<br />
5-7.5 psu<br />
0-5 psu<br />
>30 psu<br />
18-30 psu<br />
11-18 psu<br />
7.5-11 psu<br />
5-7.5 psu<br />
0-5 psu<br />
>30 psu<br />
18-30 psu<br />
11-18 psu<br />
7.5-11 psu<br />
5-7.5 psu<br />
0-5 psu<br />
>30 psu<br />
18-30 psu<br />
11-18 psu<br />
7.5-11 psu<br />
5-7.5 psu<br />
0-5 psu<br />
>30 psu<br />
18-30 psu<br />
11-18 psu<br />
7.5-11 psu<br />
5-7.5 psu<br />
0-5 psu<br />
>30 psu<br />
18-30 psu<br />
11-18 psu<br />
7.5-11 psu<br />
5-7.5 psu<br />
0-5 psu<br />
BALTIC SEA PROTECTED AREAS<br />
0 20 40 60 80<br />
Mud, non-photic zone<br />
Mud, euphotic zone<br />
Hard clay, non-photic zone<br />
Hard clay, euphotic zone<br />
Sand, non- photic zone<br />
Sand, euphotic zone<br />
Hard bottom, non -photic zone<br />
Hard bottom, euphotic zone<br />
B edrock, non -photic zone<br />
B edrock, euphotic zone<br />
Figure 7.5. Proportion of <strong>the</strong> 60 benthic mar<strong>in</strong>e landscapes represented<br />
with<strong>in</strong> BSPAs (horizontal axis). Sal<strong>in</strong>ity categories are<br />
grouped accord<strong>in</strong>g to substrate type and photic depths (vertical<br />
axis). Source: Piekä<strong>in</strong>en & Korp<strong>in</strong>en 2008.<br />
Replication can be assessed by determ<strong>in</strong><strong>in</strong>g <strong>the</strong><br />
number of spatially separated patches of each protected<br />
feature with<strong>in</strong> <strong>the</strong> network, e.g., <strong>in</strong>dividual<br />
seagrass meadows or rocky reefs. Because <strong>the</strong><br />
overall distribution of habitats and species is still<br />
%<br />
poorly known <strong>in</strong> <strong>the</strong> <strong>Baltic</strong> <strong>Sea</strong>, this cannot be fully<br />
assessed at present.<br />
Based on <strong>the</strong> <strong>in</strong>formation <strong>in</strong> <strong>the</strong> BSPA database,<br />
62 of <strong>the</strong> total of 207 species reported with<strong>in</strong> <strong>the</strong><br />
BSPA network are found <strong>in</strong> ten or more BSPAs.<br />
Of <strong>the</strong>se 62 species, 60 are birds and two are<br />
mammals. However, half of <strong>the</strong> 207 species are<br />
reported from fewer than three sites with<strong>in</strong> <strong>the</strong><br />
BSPA network. Thus, accord<strong>in</strong>g to <strong>the</strong> database,<br />
many species lack spatial replication. To fully assess<br />
<strong>the</strong> replication <strong>in</strong> <strong>the</strong> BSPA network, reliable <strong>in</strong>formation<br />
on algae, amphibians, vascular plants and<br />
<strong>in</strong>vertebrates is needed.<br />
In <strong>the</strong> BALANCE project, a spatial GIS analysis was<br />
carried out to determ<strong>in</strong>e <strong>the</strong> number of spatially<br />
separate replicates of different mar<strong>in</strong>e landscapes<br />
covered by <strong>the</strong> BSPA network. The results of <strong>the</strong><br />
analysis showed that replication of <strong>the</strong> benthic<br />
mar<strong>in</strong>e landscape patches is very variable, rang<strong>in</strong>g<br />
from zero to hundreds of replicates for different<br />
landscape types. The majority of <strong>the</strong> poorly replicated<br />
landscape types were bedrock and hard<br />
clay landscapes. The shallow euphotic bedrock<br />
landscapes had no or only one replicate, as was <strong>the</strong><br />
case for non-photic bedrock, and most euphotic<br />
and non-photic hard clay landscapes. As BSPAs are<br />
generally ra<strong>the</strong>r large, <strong>the</strong> with<strong>in</strong>-site replication<br />
of landscape patches is relatively high while <strong>the</strong><br />
number of sites host<strong>in</strong>g <strong>the</strong> replicates and <strong>the</strong>reby<br />
<strong>the</strong> between-site replication is often low. However,<br />
<strong>the</strong> ecologically mean<strong>in</strong>gful m<strong>in</strong>imum number of<br />
replicates and <strong>the</strong> m<strong>in</strong>imum size for a replicate are<br />
strongly dependent on species characteristics.<br />
Connectivity<br />
To ensure good connectivity, <strong>the</strong> BSPA network<br />
should offer sufficient opportunities for dispersal<br />
and migration of species with<strong>in</strong> and between<br />
MPAs. Connectivity depends ma<strong>in</strong>ly on <strong>the</strong> dispersal<br />
distance of <strong>the</strong> <strong>in</strong>dividual species (<strong>in</strong>clud<strong>in</strong>g<br />
larvae and juveniles) and <strong>the</strong> distance between preferred<br />
habitats for those species. Evaluat<strong>in</strong>g connectivity<br />
is somewhat problematic as <strong>the</strong> network<br />
aims to protect a wide range of species which<br />
have very different ranges of dispersal and mobility,<br />
both between species and at different stages<br />
<strong>in</strong> <strong>the</strong>ir life. Many bivalve larvae (e.g., mussels<br />
and cockles) have dispersal distances as long as<br />
100 km, while for swimm<strong>in</strong>g crustaceans and