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BENTHIC
FAUNA/COMMUNITIES
Published studies
are reviewed/summarized and laid out below for five principle areas:
-
Northumberland Strait
- Gulf
of St. Lawrence (Southern and Northern)
-
Nova Scotia (Atlantic Coast)
- New
Brunswick (Bay of Fundy)
- US
Coastal Studies
Figure 3, and the
legend that accompanies it, indicate the locations of the reviewed studies.
![](graphics/BF_fig3.gif)
FIGURE 3: Locations
of studies reviewed. See Legend on following page for locations and sources
of studies.
Legend for Figure
3 providing literature sources and locations for marine benthic studies
displayed in Figure 3.
STUDY
|
SOURCE
|
LOCATION
|
1
2
3
|
Caddy et al.,
1977
Anonymous,
1997, 1998
Scarrat &
Lowe, 1972
|
Northumberland
Strait
Northumberland
Strait
Kouchibouguac
Bay, Northumberland Strait
|
4
5
6
7
8
9
10
11
12
13
14
15
16
|
Hughes &
Thomas, 1971a
Hughes &
Thomas, 1971b
Brunel, 1971
Bourget &
Messier, 1983
Hudon &
Lamarche, 1989
Robert, 1979
Himmelman &
Lavergne, 1985
Himmelman, 1991
Jalbert et al.,
1989
Himmelman &
Dutil, 1991
Peer, 1963
Long & Lewis,
1987
Wieczorek &
Hooper, 1995
|
Bedeque Bay,
Prince Edward Island
Bideford River
estuary, Prince Edward Island
Bay of Gaspe,
Gulf of St. Lawrence
Magdalen Islands
Magdalen Islands
St. Lawrence
Estuary
St. Lawrence
Estuary
Mingan Islands
Mingan Islands
Mingan Islands
Magdalen Shallows/Laurentian
Channel
Anticostic &
Esqiman Channels
Bonne Bay, Newfoundland
|
|
Brawn et al.,
1968
Miller et al.,
1971
Peer, 1970
Volkaert, 1987
Elner &
Campbell, 1987
Hatcher et al.,
1998
Barbeau et al.,
1996
Drummond-Davis
et al., 1982
|
St. Margarets
Bay, Nova Scotia
St. Margarets
Bay, Nova Scotia
St. Margarets
Bay, Nova Scotia
St. Margarets
Bay, Nova Scotia
Southern Nova
Scotia
Southern Nova
Scotia
Southern Nova
Scotia
Southern Nova
Scotia
|
|
Caddy, 197
Wildish et al.,
1972
Wildish, 1983
Logan et al.,
1983
|
Bay of Fundy
L'Etang Inlet,
Bay of Fundy
Passamoquoddy
area, Bay of Fundy
Passamoquoddy
area, Bay of Fundy
|
29
30
31
32
33
34
35
36
37
38
39
40
41
42
|
Dexter, 1944
Dexter, 1947
Young &
Rhoads, 1971
Sanders, 1958
Sanders, 1960
Weiser, 1960
Wigley &
McIntyre, 1964
Lee, 1944
Stickney &
Stringer, 1957
MacKenzie, 1977
O'Connor, 1972
Maurer et al.,
1978
Virnstein, 1977
Day et al.,
1971
|
Ipswich Bay,
Massachusetts
Cape Ann, Massachusetts
Cape Cod Bay,
Massachusetts
Buzzards Bay,
Massachusetts
Buzzards Bay,
Massachusetts
Buzzards Bay,
Massachusetts
Martha's Vineyard,
Massachusetts
Menemsha Bight,
Massachusetts
Greenwhich Bay,
Rhode Island
Long Island
Sound, Conneticut
Moriches Bay,
Long Island, New York
Delaware Bay,
Delaware
Chesapeake Bay,
Maryland
Cape Lookout,
North Carolina
|
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3.1 NORTHUMBERLAND
STRAIT
Northumberland Strait
is that area between Prince Edward Island and the mainland of the provinces
of New Brunswick and Nova Scotia, and has water depths of 10-20 m at the
western end and >30 m at the eastern end (Kranck, 1972). The environmental
conditions within the Strait are markedly different from those prevailing
on the exposed Atlantic and lower Fundy shores (MacFarlane, 1966); conditions
within St. Georges Bay however, are largely similar to conditions in the
Strait (Moseley and MacFarlane 1969). Despite the intensive use of the
area for fisheries by three provinces, and megaproject development (Confederation
Bridge), little work has been done on the benthos in the Northumberland
Strait area.
A survey of the benthic
fauna of Northumberland Strait from the northwestern to eastern end of
Prince Edward Island was conducted in 1975 with 96 stations being occupied
taking samples from depths ranging from 5-49 m (the majority were 10-20
m deep) (Caddy et al., 1977). Bottom sediments were composed of gravel/coarser
material, sand, and silt/clay. The Strait was divided into four areas
(A-D) of which Area D, with a substrate of principally mud and mud-clay,
is immediately adjacent to St. Georges Bay. Results are summarized here
for both the entire Strait as well as Area D. Seventy four species of
algae (43 species of Rhodophyta, 27 species Phaeophyta, 2 species each
of Chlorophyta and Cyanophyta) were found with the most commonly occurring
(>50% of samples) being Phyllophora spp., Polysiphonia spp.,
and Laminaria longicruris. Species found in 25-50% of samples included
Ectocarpus siliculosus, Desmarestia aculeata, Fucus
spp., Cystoclonium purpureum, Rhodomela confervoides, and
Rhodymenia palmata.
Benthic macrofauna
results from van Veen grab samples are presented in Table 1 including
both the Strait as a whole and Area D. A complete species list of the
343 invertebrate species collected from this sampling program is presented
in Appendix 3. Polychaetes indicate the greatest species abundance followed
by amphipods, bivalves and arthropods, gastropods, and finally echinoderms.
Sampling by beam trawl and scallop dredge indicated that echinoderms (Asterias
vulgaris [64% of stations], Henricia sanguinolenta [53%], Echinarachinus
parma [47%]) were the most widespread benthic fauna. Of 25 bivalve
species sampled by trawl the mussels Modiolus modiolus (35.5% of
stations) and Mytilus edulis (31.3%) were most common. Of 37 gastropod
species the most commonly encountered were Nassarius trivittatus
(21% of stations), Lunatia heros (17%) and Neptunea decemcostata
(14%). The most common arthropods, excluding the prevalent amphipods,
were Crangon septemspinosa (36% of stations), Pagurus acadianus
(30%), and Pandalus montagui (21%). Other commonly encountered
fauna included hydroids (51% of stations), bryozoans (47%) and Porifera
(47%).
Table 1. Number of
species, families, and most common species captured in Northumberland
Strait in 1975 in van Veen grab samples. Area D is that portion of the
Northumberland Strait study area immediately adjacent to St. Georges Bay.
Data from Caddy et al. (1977).
|
Northumberland Strait
|
Area D
|
|
# of species
|
# of families
|
Most common species
|
# of species
|
# of families
|
Most common species
|
Bivalves |
26
|
13
|
Asarte undata
Clinocardium ciliatum
Tellina agilis
Thyasira gouldii
|
19
|
11
|
Clinocardium ciliatum
Modiolus modiolus
Nucula tenuis
Thyasira gouldii
Yoldia sapotilla |
Gastropods |
16
|
12
|
Nassarius trivittatus
Retusa canaliculata |
5
|
4
|
Admete couthouyi
Oenopta (Lora) elegans
Oenopta turricula |
Polychaetes |
91
|
29
|
Ninoe nigripes
Pholoe minuta
Prionospio steenstrupi |
58
|
25
|
Pholoe minuta
Prionospio sttenstrupi
Spio sp. |
Arthropods |
26
|
13
|
Aeginina longicornis
Diastylis quadraspinosa
Diastylis sculpta
Eudorella trunculata |
16
|
8
|
Diastylis quadraspinosa
Eudorella emarginata
Eudorella trunculata
Leucon nasica |
Amphipods |
73
|
19
|
Ampelisca macrocephala
Ampelisca vadorum
Corophium bonelli
Phoxocephalus holbolli
Unciola irrorata |
41
|
17
|
Ampelisca macrocephala
Byblis gaimardi
Corophium bonelli
Harpinia propinqua
Phoxocephalus holbolli |
Echinoderms |
6
|
|
Echinarachinus parma
Ophiura robusta |
5
|
5
|
Asterias vulgaris
Ophiura robusta
Stongylocentrotusdrobachiensis |
In terms of biomass,
the echinoderms contributed the majority in the western half of Northumberland
Strait (41.1-86.38% of total biomass). The polychaetes, bivalves and gastropods
made up 13-28% of the biomass in this area and arthropods <2%. In Area
D however, adjacent to St. Georges Bay, bivalves contributed greatest
to the biomass (42.48%) followed by polychaetes (25.18%) echinoderms (15.13%),
gastropods (2.32%), and arthropods (0.62%). Other species not falling
into these taxa account for 14.26 %. Biomass of fauna (g wet weight/m2)
for the whole Strait ranged from 0.01-750.6 for polychaetes, 0.01-112.6
for bivalves, 0.01-137.1 for gastropods, 0.01-555.2 for echinoderms, and
0.01-19.3 for arthropods. Within Area D total biomass (all taxa combined)
ranged from 2.25-141.6 g wet weight/m2, with biomass of individual
taxa ranging as: polychaetes (0.3-750.6 g wet weight/m2), bivalves
(0.44-112.6), gastropods (0.21-123.2), echinoderms (0.01-418.1) and arthropods
(1.52-608.1).
In 1967, Scarrat and
Lowe (1972) conducted a study on the biology of the rock crab (Cancer
irroratus) in Kouchibouguac Bay. Sampling between 4 and 18 m depth
these authors found a standing stock ranging from 0.7 to 3.8 g/m2,
with the greater values being found on boulders in both the spring and
fall.
In 1980, Dunbar et
al. (1980) compiled existing information to "describe and map the known
distribution of the marine communities and faunal and floral elements
in the Gulf of St. Lawrence". Benthic invertebrates and algae reported
by these authors in the vicinity of the St. Georges Bay study area are
listed in Table 2. Due to the paucity of information on the St. Georges
Bay area, the mobility of invertebrates, and the prevailing currents from
west through the Strait into St. Georges Bay, distribution information
from Dunbar et al. (1980) was extracted from as distant as the eastern
point of P.E.I. and westward to Pictou Harbour. Dunbar et al. (1980) emphasize
that the blank areas on their charts from which this information is drawn
are not reflective of absence of a given species but often these areas
have not been sampled to determine presence. Thus, the list derived from
their work is not to be construed as thorough or complete. Further sampling
is required to establish presence and distributions of most components
of the benthic flora and fauna.
Table 2. Species list
for St. Georges Bay area and eastern Northumberland Strait from Dunbar
et al. (1980).
Algae
|
Macroinvertebrates
|
Phaeophycea |
Laminaria digitata
Laminaria saccorhina
Pilayella littoralis
|
Bivalvia |
Arctica islandica
Astarte subaequilatera
Astarte undata
Clinocardium ciliatum Crassostrea virginica
Crenella glandula
Macoma tenta
Mercenaria mercenaria
Mulina lateralis
Mya arenia
Mya truncata
Nucula proxima
Nucula tenuis
Pandora glacialis
Periploma leanum
Petricola pholadiformis
Pitar morrhuana
Placopecten magellanicus Teredo navalis
Yoldia limatula
Volsella modiolus
Yoldia sapotilla
Yoldia thraciaeformis |
Rhodophyta |
Ceramium fastigatum
Ceramium rubrum
Euthora cristata
Polysiphonia harveyi Polysiphonia urceolata Rhodymenia palmata
Trailliella intricata |
Gastropoda |
Acmaea testudinalis
Admete couthouyi
Buccinum undatum
Crepidula fornicata
Crepidula plana
Nassarius trivittatus
Polineces heros
Polineces immaculata Urosalpinix cinerea |
Chlorophyta |
Enteromorpha linza
Ulva lactuca |
Polyplacophora |
Ischnochiton ruber
Ischnochiton alba |
|
|
Crustacea |
Cancer irroratus
Crangon septemspinosa Homarus americanus
Pagurus acadianus |
Construction through
the mid-1990s of the Confederation Bridge linking New Brunswick with Prince
Edward Island resulted in the examination of benthic fauna and flora as
part of an Environmental Impact Assessment. The two principle sampling
methods were direct observation, by SCUBA and Remotely Operated Vehicles
(ROV), and colonisation studies of organisms on the newly placed piers.
The water depths ranged from 5 to 25 m and substrate was primarily cobble,
shell, sand, and silt but with some bedrock and boulders. The following
discussion is drawn from Anonymous (1997, 1998). Underwater video indicated
only a few macrobenthic invertebrates. These were Homarus americanus,
Cancer irroratus, Placopecten magellanicus, Pagurus
sp., Metridium sp., Mytilus edulis, Asterias sp.
Modiolus modiolus, hydrozoans and poriferans. Calculated densities
based on this video for the prominent species were 0-0.04 individuals/m2
for H. americanus, 0-0.32/m2 for C. irroratus,
0-0.056/m2 for P. magellanicus, and 0-0.012/m2
for Pagurus sp. In a dredge disposal site in Amherst Cove, Homarus
americanus densities were almost consistently zero animals/m2
between 1994 and 1997 though occasionally did rise to 0.6/m2.
Cancer irroratus in this same time period ranged from 0 to 2.23
animals/m2, though 1/m2 may be more representative
of maximum density.
The colonisation study
of piers in Northumberland Strait (Table 3) indicate quite evenly distributed
species numbers between the three phyla of algae and 11 phyla/classes
of invertebrates. The bivalves, gastropods, polychaetes and crustaceans
together only account for 54% of the 68 species recorded. The bryozoans,
hydroids and poriferans also contribute significantly to the total species
present (together accounting for 25% of species present). Unfortunately
biomass was not recorded in this survey, instead presence was quantified
by percent cover. On the piers the dominant faunal and floral groups in
1996-97 were (approximated from Figures 4.23-4.26 in Anonymous 1998):
0-5 m depth
- Barnacles (20-60% cover), Enteromorpha (25-45% cover), algal
mat (5-80% cover), bryozoans/hydrozoans (5-25% cover) and mussels (generally
< 15% cover).
5-10 m depth
- Barnacles (25-40% cover), algal mat (20-30% cover), bryozoans/hydrozoans
(<5-45% cover), and sea anenomes (5 - 20% cover).
10-15 m depth
- Barnacles (20-40% cover), algal mat (15-85% cover), bryozoans/hydrozoans
(20-45% cover), sea anenomes (5 - 25% cover) and sea stars (0 - 25%
cover).
15-20 m depth
- Barnacles (10-45% cover), bryozoans/hydrozoans (10-55% cover) and
sea anenomes (10 - 30% cover).
20-25 m depth
- Barnacles (25-40% cover), bryozoans/hydrozoans (10-50% cover) and
sea anenomes (5 - 35% cover).
>25 m depth
- Barnacles (15 - 35% cover), bryozoans/hydrozoans (20-55% cover), algal
mat (5-20% cover), and sea anenomes (5-30% cover)
Table 3. Species list
of algae and invertebrates reported from two years (1996, 1997) sampling
in Northumberland Strait in 5-20m of water as part of Confederation Bridge
Project. Table compiled from Anonymous, 1997 9Talbes 5.7-5.100 and 1998
(Tables 4.2-4.12).
Algae
|
Invertebrates
|
Phaeophyta |
Asperococcus echinatus
Chorda filum
Chordaria flagelliformis Eudesme virescens
Fucus serratus
Saccorhiza dermatodea |
Bryozoa |
Averillia sp.
Bryozoa membranacea
Bugula turrita
Flustra foliacea
Membranipora sp. Schizoporella unicornis |
Chlorophyta |
Chaetomorpha melangonium Chaetomorpha sp.
Cladomorpha sp.
Cladophora albida
Cladophora seriacea
Cladophora sp.
Enteromorpha (2 species) |
Hydroid |
Bougainvillia sp.
Campanularia calceolifera Campanularia sp.
Hydractinia sp.
Sertularia argentea
Sertularia sp.
Tubularia crocea
Tubularia sp. |
Rhodophyta |
Antithamnion sp.
Ceramium (2 species) Ceramium rubrum
Chondrus crispus
Corallina offinalis
Cystoclonium ceranoides Gelidium sp.
Phyllophora pseudoceranoides Polysiphonia nigrescens Polysiphonia
sp. Spermothamnion repens Spermothamnion sp. |
Nematode |
Nematoda |
|
|
Porifera |
Halichondria bowerbanki Scypha ciliata
Scypha sp. |
Anthozoa |
Metridium senile
Metridium sp.
Tealia felina
Tealia crassicornis
|
Bivalvia |
Anomia simplex
Gammarus sp.
Hiatella arctica
Modiolus modiolus
Modiolus sp.
Mytilus edulis
Mytilus sp.
Spisula solidissima |
Gastropoda |
Aeolidia papillosa
Coryphella sp.
Crepidula convexa
Crepidula fornicata
Crepidula plana
Dendronotus frondosus Eubranchus sp.
Facelina bostoniensis
Lacuna vincta
Littorina sp.
Mitrella lunata
Nassarius trivittatus
Notoacmaea testudinalis Onchidoris |
Polychaeta |
Eulalia viridis
Eusyllis blomstrandi
Gattyana cirrosa
Harmothoe sp.
Neries sp.
Polydora ciliata
Phyllodoce sp. |
Crustacea |
Aeginella longicornis
Balanus balanoides
Balanus sp.
Cancer irroratus
Caprella linearis
Caprella sp.
Corophium volutator
Homarus americanus
Jassa falcata
Pagurus acadianus
Pagurus pubescens |
Pycnogoda |
Phoxocilidium femoratum |
Echinodermata |
Asterias forbesi
Asterias vulgaris
Henricia sp. |
Tunicata |
Thaiacea (salp)
Doliolum sp. |
Summary
of Northumberland Strait
Based
on the reported sampling from Northumberland Strait between 1967 and 1998
it appears that polychaetes are present in the greatest species abundance
(up to 91 species) followed by amphipods (up to 73 sp.), bivalves (up
to 26 sp.), gastropods (up to 16 sp.), and non-amphipod crustaceans and
echinoderms each up to 6 species present. Algal species are present in
the range of 3-27 species (Phaeophyta), 7-43 species (Rhodophyta), and
2-8 species (Chlorophyta).
Biomass
ranges up to 1,400 g/m2 with bivalves, gastropods, polychaetes
and echinoderms making up the majority of the contribution. The biomass
is generally greatest for the larger organisms (echinoderms and bivalves),
with lower contributions by the polychaetes, gastropods and arthropods.
However, this large contribution by molluscs and echinoderms includes
inedible tests/skeletons etc., and so it is questionable how relevant
these biomass estimates are from a trophic level perspective, as much
of the greatest biomass contribution may not be passed on to consumers.
Common invertebrate species reported in Northumberland Strait (from Tables
1-3) include 31 bivalves, 23 gastropods, 11 polychaete species, 25 arthropods
and 6 echinoderms. The most commonly encountered species in this limited
sampling of Northumberland Strait were:
Bivalves: Modiolus
modiolus, Mytilus edulis, Placopecten magellanicus
Gastropods:
Nassarius trivittatus, Lunatia heros, Neptunea decemcostata
Arthropods:
Crangon septemspinosa, Pagurus acadianus, Pandalus montagui, Homarus
americanus, Cancer irroratus
Echinoderms:
Asterias vulgaris, Henricia sanguinolenta, Echinarachinus parma
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3.2
GULF OF ST. LAWRENCE
The fauna
and subtidal communities of the Gulf of St. Lawrence are poorly known
(Robert, 1979; Long and Lewis, 1987), except perhaps in qualitative or
semi-quantitative terms (Bourget and Messier, 1983). The Gulf is a very
large embayment composed of many different localized environments with
differing factors (e.g., depth, temperature, salinity, substrate, etc.)
affecting benthic community organization and structure. There appears
to be different community structures and controls between the southern
and northern Gulf; in the southern Gulf decapod crustaceans and fishes
are thought to be influential in controlling community structure, while
their absence in the northern Gulf results in whelks and seastars filling
these predatory roles (Himmelman, 1991). The fauna and flora of the estuary
itself are subarctic and boreal, more closely resembling the north shore
of the Gulf and the Labrador coast than the southern Gulf and Maritimes
(Himmelman and Lavergne, 1985). These differences must be kept in mind
in the descriptions of the various studies below.
3.2.1
Southern Gulf
Sampling
was conducted in the Bay of Gaspe between 1956 and 1960 involving 91 stations
at depths of 9-100 m on substrates of sand, muddy sand, and mud (Brunel,
1971). Nineteen polychaete species were reported (two most common: Harmothoe
extenuata and Gattyana cirrosa), as well as 11 bivalve species
(most common: Serripes groenlandica, Clinocardium ciliatum,
Spisula polynyma), 17 decapod crustaceans (most common: Sabinea
septemcarinata, Argis dentata, Eualus macilentus), and
12 echinoderms (Ophiuri sarsi and Asterias vulgaris most
common). The author recognized eight communities within this area; these
are presented with their species in Table 4.
Table
4. Communities recognized in the Bay of Gaspe, 1956-1960. Data from Brunel
(1971).
Euryboreal Soft Mud
|
Euryboreal Sand
|
Euryboreal Mixed Ground
|
Casco bigelowi
Chiridotea tuftsi
Diastylis polita
Nephthys incisa
Pholoe minuta
Phyllodoce mucosa
|
Asteria vulgaris
Bostrichobranchus pilularis
Chiridotea tuftsi
Crangon septemspinosa
Diastylis polita
Echinarachinus parma
Edotea triloba
Hippomedon serratus
Photis macrocoxa
Phoxocephalus holbolli
Phyllodoce mucosa
Spisula polynyma
Tmetonyx nobilis
|
Ophiopholis aculeata
Ophiura robusta
Strongylocentrotus drobachiensis
|
Subarctic Muddy Sand
|
|
Subarctic Sandy Mud
|
Cerastoderma pinnulatum
Clinocardium ciliatum
Leptocheirus pinguis
Macoma calcarea
Ophiura sarsi
Serripes groenlandica
Sternaspis scutata
Thyasira gouldii
|
Aporrhais occidentalis
Gattyana cirrosa
Harmothoe extenuata
Harmothoe imbricata
Harmothoe nodosa
Macoma calcarea
Maldane sarsi
Mya truncata
Nuculana pernula
Ophiura sarsi
Priapulus caudatus
Sabina septemcarintat
Serripes groenlandica
Steguphiura nodosa
Yoldia norvegica
|
Arctic Cohesive Mud
|
Arctic Sandy & Pebbly Mud
|
Arctic Mixed Ground
|
Arrhis phyllonyx
Chionoecetes opilio
Ctenodiscus crispatus
Eualus macilentus
Neohela monstrosa
Spiochaeopterus sp.
|
Boltenia ovifera
Ophiura sarsi
|
Chlamys islandica
Ophiocantha bidentata
Ophiopholis aculatea
Ophiura robusta
Ophiura sarsi
Strongylocentrotus pallidus
|
In a
classification and ordination exercise, Hughes and Thomas (1971a) delineated
six groups within a Bedeque Bay, Prince Edward Island estuary from samples
collected in 1967 from depths of 0.3 to 5.4 m (substrate description not
provided). However, for the purposes of this paper only their first division,
into euryhaline and lower estuarine species, is relevant. Their further
divisions are of fine scale and statistical divisions; their biological
or field assessment would be problematic in trying to define other areas
with respect to these communities due to great variability in environmental
and biological conditions. Their species groupings are presented in Table
5. These authors reported 62 species of which 20 are polychaetes, 14 bivalves,
9 gastropods, 6 crustaceans, 1 echinoderm and 8 algae species accounting
for 93.5% of the total species number. Dominant species (i.e., > 50 individuals/m2
or >50 g dry weight/m2 for plants) at this location were Mytilus
edulis, Tellina agilis, Nassarius obsoletus, Nassarius
trivittatus, Littorina littorea, Crepidula plana, Lunatia
heros, Polycirrus eximius, Neopanpoe texana, Balanus
improvisus, Nemertea, Ulva lactuca, Chondrus crispus,
Gracilaria verrucosa, and Zostera marina.
Table
5. Large scale division of estuarine species from Bedeque Bay, Prince
Edward Island, 1967. Table modified from Hughes and Thomas (1971a).
Euryhaline
|
Lower Estuarine
|
Bivalvia |
Crassostrea virginica
Mulinia lateralis
Mytilus edulis
Petricola pholadiformis
Venus mercenaria |
Bivalvia |
Ensis directus
Mya arenia
Pitar morrhuana
Tellina agilis |
Gastropoda |
Crepidula fornicata
Crepidula plana
Littorina littorea
Nassarius obsoletus |
Gastropoda |
Lunatia heros
Nassarius trivittatus |
Polychaeta |
Glycera americanus
Harmothoe imbricata
Nereis virens
Notomastus latericeus Scoloplos fragilis |
Polychaeta |
Glycera dibranchiata
Maldanopsis elongata
Nephthys incisa
Pectinaria gouldii
Pectinaria granulata
Pherusa affinis |
Crustacea |
Balanus improvisus
Cancer borealis
Crangon septemspinosa Neopanope texana |
Crustacea |
Pandora gouldiana |
Plantae |
Chondrus crispus Enteromorpha prolifera Gracilaria
verrucos
Phyllophora sp.
Polysiphonia grescens
Ulva lactuca
Zostera marina |
Amphipoda |
Leptocheiros pinguis |
|
|
Echinodermata |
Asterias vulgaris |
In an
analysis of a second Prince Edward Island estuary (Bideford River; sampling
date not provided), Hughes and Thomas (1971b) collected benthic samples
along four transects ranging in depths from intertidal to 4.7 m and substrates
ranging from silt-clay to coarse sand (median particle size range 0.0085-0.79
mm). The most commonly captured invertebrates are provided in Table 6.
Table
6. Ranges of densities and biomass of common invertebrates (>20/m2
for transect 1-3; >100/m2 for transect 4) from Bideford
River estuary, Prince Edward Island. Data from Hughes and Thomas (1971b).
|
Species
|
Density (/m2)
|
Biomass (g dry weight/m2) |
Bivalvia |
Cumingia tellinoides
Gemma gemma
Macoma balthica
Modiolus demissus
Mya arenia
Mytilus edulis
Tellina agilis |
2-300
5-29,120
1-286
1-42
1-565
1-273
1-438
|
0.01-2.33
0.01-16.32
0.01-6.47
0.37-18.02
0.01-189.97
0.47-157.28
0.01-1.03
|
Gastropoda |
Crepidula fornicata
Crepidula plana
Littorina saxitalis
Nassarius obsoletus
Odostomia sp.
Retusa canaliculata |
1-688
1-334
1-1,500
1-1,557
15-441
10-300
|
0.01-25.4
0.01-7.09
0.02-6.0
0.02-37.76
0.01-4.97
0.01-0.68
|
Polychaeta |
Clymenella torquata
Harmothoe imbricata
Nereis succina
Nereis virens
Notomastus latericeus
Pectinaria gouldii
Scalopolos fragilis |
2-780
2-260
2-134
1-790
12-875
2-264
1-170
|
0.01-3.59
0.01-1.04
0.04-0.49
0.01-11.33
0.01-0.52
0.02-0.59
0.01-0.59
|
Amphipoda |
Corophium insidiosum
Gammarus locusta |
30-570
1-120
|
0.01-0.22
0.01-0.19
|
Isopoda |
Leptochelia rapex |
100-375
|
0.01-0.06
|
Unclassified |
Mysella planulata |
40-375
|
0.02-0.18
|
A Magdalen
Island lagoon (maximum depth 8 m) was sampled in 1975 for macrobenthos
density and biomass (Bourget and Messier, 1983). The substrate was predominantly
sands with minor amounts of silt, clay and gravel (median particle diameter
0.25 mm). Fifty four benthic species were reported with a mean subtidal
density of 3,398.1 individuals/m2 and mean biomass of 6.4 g/m2.
The most common (i.e., present in highest density) organisms were the
bivalve Gemma gemma (1,398.7 /m2), the gastropods Littorina
saxatillis (1,345.6 /m2), Cingula aculeus and Hydrobia
minuta (526.7 and 524.8 /m2 respectively), and the crustacean
Corophium insidiosum (771.2 /m2). All other species
were present at less than 500 individuals/m2. Table 7 presents
ranges of values for individual densities and biomass for this area.
Table
7. Ranges of individual species densities and biomass grouped by Phyla/class
for Magdalen Islands sampled in 1975. Data from Bourget and Messier (1983).
|
Individual Density (/m2)
|
Biomass (g dry wt./m2)*
|
Sipuncula |
1.6-1.8
|
|
Mollusca
Gastropoda
Bivalvia
|
|
0.578-1.249 (13.1-14.4)
0.407-2.344 (6.4-32.8)
|
Polychaeta |
1.1-92.5
|
2.2-3.943 (33.6-62.1)
|
Crustacea |
1.0-771.2
|
0,1-2,151 (2.3-24.9)
|
* range in brackets is percent biomass
The Magdalen Island
lagoons were sampled again in 1985 (Hudon and Lamarche, 1989), this time
by SCUBA. Lobster (Homarus americanus) densities were found to
range from 0.018-0.975 lobster/m2 and rock crab (Cancer
irroratus) from 0.008 to 3.358 crab/m2. Four major substrate
types were identified and the associated flora and fauna are listed below:
Small stones
imbedded in soft sediments - Algae - Ptilota serrata, Chordaria
tomentosa, Corallina officinalis. Invertebrates - Mytilus edulis,
Modiolus modiolus, polychaetes (particularly Lepidonotus squamatus),
littorinid gastropods, hydroids, barnacles, brittle stars.
Bedrock (sandstone)
- similar to above
Piles of large
rocks - Algae -Laminaria spp., Ulva spp., Chondrus
crispus, Chordaria tomentosa, Rhodomenia palmata. Invertebrates
- Caprellid amphipods, Strongylocentrotus drobachiensis, gastropods
(Lacuna vincta, Nassarius sp.), Mytilus edulis, Modiolus modiolus,
hydroids, ascidians, Porifera, nereid polychaetes.
Sand - Zostera
marina, Ulothryx. Invertebrates - Echinarachinus parma, polychaetes,
burrowing bivalves (Venus mercenaria, Ensis directus, Mya arenia,
Crangon septemspinosa).
Back
To Top
3.2.2
Northern Gulf
In 1962
benthic sampling was undertaken in the northern Gulf of St. Lawrence along
the northeast edge of the Magdalen Shallows and the Laurentian Channel
(Peer, 1963). Two of the stations (Stations 26 & 78) were within the depth
range of the St. Georges Bay study area; at depths of 73 and 86 m respectively.
Station 26 had a substrate of unsorted gravel and Station 78 substrate
was fine sand. Thirty one taxa were identified from Station 26, with Yoldia
myalis (15.5%), Strongylocentotus droebachiensis (13.9%), polychaetes
(12.1%), and Gephryea (11.7%) each contributing the greatest presence.
Pagurus spp. (9.0%), Ophiuridea (7.3%), and Coelenterata (7.1%)
contributed between 5 and 10% each, and the remaining 22 taxa each contributed
<5% to the standing crop. Estimated biomass at this station was 6.16 g
dry organic matter/m2. Seventeen taxa at this site made up
95% of the biomass. Station 78, on fine sand, was dominated by the sand
dollar Echinarachinus parma (78.8% of standing crop) with much
lesser contributions by Ophiuroidea (9.3%) and 28 other taxa. Estimated
biomass at Station 78 was 21.59 g organic matter/m2. At this
station 95% of the biomass was represented by five taxa (E. parma,
Ophiuroidea, Priscillina armata, Pectinaria spp., and Macoma
balthica).
Long
and Lewis (1987) report results of a 1981 sampling program in Anticosti
and Esquiman Channels in the northern Gulf. Sample depths ranged from
37 to 285 m; only results from less than 150 m depth are included in Table
8. The substrate at the stations sampled was largely sand (0.062-1.0 mm)
and gravel (1.0-64 mm), with some (generally <35%) pelite (<0.062 mm).
They report 73 taxa collected when all of their sites (including the deep
stations) are included of which 25 are molluscs, 22 are polychaetes, 9
amphipods, 4 echinoderms and the remainder as Cumacea (3 taxa), Cnidaria
(3 taxa) and Other Phyla (6 taxa). They found that, in general, benthic
diversity was maximum between 75 and 94 m and appeared to be highest on
shelf/slope breaks and decreased to moderate levels on slopes. This is
in agreement with Robert (1979) who found in a cluster analysis of environmental
and biological variables in the St. Lawrence Estuary that there is a complete
distinction between their sampled stations above and below 75 m depth.
Robert (1979) also reports the shallower stations having the greatest
diversity. However, though diversity decreased on slopes, abundance was
high (Long and Lewis, 1987). Within depths representative of the St. Georges
Bay study area the range of substrate component values in the study of
Long and Lewis (1987) was from 5-98% pelites, 8-71% sand, and 4-32% gravel.
Macrobenthos abundance ranged from 640 to 5,250 individuals/m2
and diversity (Shannon Weaver H') from 0.746-1.234.
Table
8. Depth, abundance and diversity/evenness indices of samples from the
Anticosti and Esquiman Channels, 1981. Table modified from Long and Lewis
(1987).
Depth (m)
|
Abundance (/m2)
|
Diversity Index (H')*
|
Evenness Index (J)
|
37
40
55
55
65
66
70
70
75
75
78
92
95
95
95
96
125
130
135
|
1,030
2,875
640
3,750
1,685
2,160
1,365
750
730
2,310
3,056
2,540
1,596
1,896
5,250
2,932
3,775
4,120
672
|
1.089
1.092
1.212
1.299
1.205
1.132
1.029
1.234
0.746
1.114
1.132
0.071
1.205
1.078
1.226
1.176
0.993
1.129
0.984
|
0.236
0.193
0.292
0.219
0.278
0.211
0.299
0.286
0.174
0.208
0.211
0.239
0.252
0.247
0.196
0.243
0.171
0.188
0.269
|
* H'=Shannon Weaver diversity index
Himmelman
(1991) provides qualitative description of the communities to depths of
20 m on four different substrate types from the Mingan Islands, northern
Gulf of St. Lawrence. Macrobenthic species and principle algal species
reported are presented below for three of his descriptions - 1) Moderately
exposed, medium sloped bottoms, 2) Rocky faces; and 3) Gently sloping
sediment bottoms in areas of strong tidal currents. These areas are thought
to physically represent some of the areas within the St. Georges Bay study
area though the previous caveat about differences in biotic communities
between the southern and northern Gulf must be borne in mind.
Moderately exposed,
medium sloped bottoms
- 4-6 m depth to
bottom of rocky zone - Ophiopholis aculeata, Halocynthia pyriformis,
Metridium senile, Tealia felina, Psolus fabricii and Cucumaria
frondosa. Algal species Alaria sp., Saccorhiza dermatodea,
Laminaria digitata, L. longicruris, Agarum cribrosum
- sediment bottoms
below rocky slopes - Echinarachinus parma, Clinocardium ciliatum,
Serripes groenlandica, and Spisula polynyma.
Rocky
faces
- Ophiopholis
aculeata, Halocynthia pyriformis, Metridium senile, Tealia felina, Myriopora
subgrucila, Pallina sitiens.
Gently
sloping sediment bottoms in areas of strong tidal currents
- Gersemia
sp., Cucumaria frondosa, Echinarachinus parma, Psolus fabricii, Boltenia
ovifera, Halocynthia pyriformis, Metridium senile, Lurcenaria quadricornis,
Chlamys islandica, Tealia felina, Gorgonocephalus arcticus, Ophiura
sarsi, Buccinum undatum, Aporrhais occidentalis. Algal species Agarum
sp., Ptilota sp.
Himmelman
(1991) also reports densities for predatory invertebrates in the Mingan
Island area. The whelk Buccinum undatum had the highest density
(0.417 /m2), four seastar species (Leptasterias polaris,
Asterias vulgaris, Crossater paposus, and Solaster endeca)
ranged from 0.002 to 0.15 /m2 and the crabs Hyas araneus
(0.055 /m2) and Cancer irroratus (0.053 /m2)
were also present at low densities. The gastropod Neptunea despecta
tornata was only present at a density of 0.006 /m2. During
1982-1983, in this area the mean density of Buccinum undatum was
found to range from 1.25 to 2.86 individuals/m2 between 0 and
20 m water depth with biomass estimates including 1.2 g/m2
(juveniles), 6.2 g/m2 (immatures) and 23.0 g/m2
(mature animals) (Jalbert et al., 1989). Densities of other species reported
by Jalbert et al. (1989) are provided in Table 9. The percentage occurrence
of various species by substrate are provided in Table 10. In this area
the urchin Strongylocentratus drobachiensis is the most abundant
organism on all substrates, with four each of bivalve and gastropod species,
two other echinoderms, and a single polychaete species forming the remainder
of the most commonly occuring species. Based on 1984 SCUBA sampling at
the Mingan Islands, Himmelman and Dutil (1991) report the seastars Asterias
vulgaris and Leptastarias polaris at densities <0.25/m2
at depths below 2 m (though up to 1.71/m2 in depths of 0-2
m). Crossater papposus is consistently below 0.03 individuals/m2.
These results must be qualified, however, as Himmelman and Dutil (1991)
point out that the reduced number of fish in the northern Gulf acting
as predators relative to the Maritimes, and the resultant importance of
seastars and whelks, suggest major differences in community structure
between the two areas.
Table
9. Estimated densities of selected invertebrates from Mingan Islands,
Quebec, 1982-83. Data from Jalbert et al. (1989).
Species |
Depth (m)
|
Density (/m2)
|
Gastropoda
Aporrhais occidentalis
Neptunea despecta
|
14-20
<10
|
0.22-0.27
0.01-0.06
|
Crustacea
Hyas araneus
Pagurus sp.
|
0-8
8-20
0-2
18-20
|
0.06-0.08
<0.045
1.13
4.94
|
Echinodermata
Astetias vulgaris
Crossater paposus
Letastaria polaris
Solaster endeca
|
4-8
12-20
0-20
4-8
16-20
0-20
|
0.19
0.01-0.03
0.01
0.74
0.06
0.002
|
Table
10. Occurrence (percentage presence in sampled quadrats) of various invertebrate
and algal species on various substrates near the Mingan Islands, 1982-83.
Table from Jalbert et al. (1989).
Species |
Bedrock
|
Boulders
|
Cobbles
|
Gravel
|
Sand-Mud
|
Bivalvia
Chlamys islandica
Hiatella arctica
Mya truncata
Mytilus edulis
Other large clams
|
0
47.3
11.3
19.4
0.4
|
1.8
22.9
17.3
21.8
2.1
|
10.9
8.3
39.8
10.2
8.3
|
1.0
6.9
32.7
6.9
7.9
|
0.9
1.7
47.2
2.7
24.3
|
Gastropoda
Acmeae testudinalis
Littorina sp.
Margarites sp.
Tonicella sp. |
40.3
14.5
17.3
38.9
|
73.6
11.6
34.5
46.1
|
53.0
12.4
18.8
38.7
|
45.5
5.0
4.0
31.7
|
17.7
2.7
6.1
9.4
|
Polychaeta
Pectinarea granulata |
6.7
|
9.9
|
28.2
|
10.9
|
13.2
|
Echinodermata
Echinarachinus parma
Ophiopholis aculeata
Strongylocentrotus drobachiensis |
0
75.3
95.8
|
2.8
57.0
92.6
|
11.7
43.2
94.7
|
21.8
9.9
87.1
|
29.9
9.7
87.2
|
Algae
Agarum cribrosum
Alaria esulenta
Ptilota serrata |
20.8
7.4
34.3
|
14.8
6.0
7.0
|
9.4
3.0
16.9
|
5.9
2.0
5.0
|
1.7
0.4
9.8
|
Sampling
in the St. Lawrence estuary from 1970-72 is reported for mollusc species
by Robert (1979). Sampling at stations between 15 and >365 m depth over
sediments of silt-sand, silt-clay, and sand-silt (median particle diameter
<0.063 - 0.25 mm) resulted in 52 mollusc species (Bivalvia = 32 species,
Gastropoda = 16, Scaphapoda = 2, Polyplacophora = 1, Aplacophora = 1 species).
Combined, the bivalves and gastropods represented 92% of the total mollusc
species present. As stated previously, Robert (1979) found the highest
diversity in shallow water and also suggests that sediment type is a more
precise determinant than water temperature with respect to organism presence/absence.
Robert (1979) also found that when diversity is high, the dominant molluscan
species is not exceedingly abundant (<200 individuals) and is always a
suspension feeder. He clustered mollusc 'assemblages' by species present
and environmental variables (temperature, substrate) and two of the resultant
clusters may be relevant to the St. Georges Bay study area (Table 11)
despite the differences between the northern Gulf and the Maritimes. The
number of species and individuals per sample, and diversity indices, are
generally lower for the deeper group than the shallow water group.
Table
11. Range of diversity and eveness indices (Group A, n=13, Group F, n=10)
of molluscan fauna in two depth ranges from the St. Lawrence Estuary,
1970-1972. Table adapted from Robert (1979).
|
Group A (<75m depth)
|
Group F (86-165m depth)
|
Number of species per sample (S) |
15-34
|
8-18
|
Number of individuals per sample (N) |
121-1140
|
64-631
|
Brillions diversity index (H) |
0.18-0.98
|
0.1-0.59
|
Shannon Weaver diversity index (H') |
0.17-0.99
|
0.1-0.66
|
Hmax |
1.17-1.53
|
0.9-1.26
|
Evenness (J) |
0.14-0.74
|
0.11-0.57
|
Hmax=log(S)
Himmelman and Lavergne
(1985) identify four subtidal zones in the St. Lawrence Estuary based
on 111 SCUBA diving transects. Their results are on rocky, shallow (<12
m) shorelines and their zonation is presented in Table 12. The Fringe
Algal Zone extends from the low intertidal to a depth up to 4 m below
Lowest Water at Spring tides (LWST). The Zone of Grazing-Resistant Algae
is immediately below this, and at greater depth is the Barren Zone; an
area lacking in species and unproductive. Finally, the Zone of Filter
Feeders is found in the St. Lawrence Estuary at depths where the urchin
density is much reduced, generally 4-10 m depth. The depths of these zones,
if present in the St. Georges Bay study area, are unlikely to coincide
with the depths reported here as the local conditions are different between
the St. Lawrence estuary and the west coast of Nova Scotia.
Table 12. Characteristic
species of the subtidal zonation of the St. Lawrence Estuary shallow water
(<12 m) zones. Table modified from Himmelman and Lavergne (1985)
|
Algae |
Invertebrates |
Fringe Algal Zone |
Alaria esculanta
Chordaria flagelliformis
Desmarestia aculeata
Halosaccion ramentaceum
Laminaria spp.
Palmaria palmata
Petalonia fascia
Polysiphonia urceolata
Porphyra spp.
Rhodomela confervoides
Saccorhiza dermatodea
Spongomorpha arcta
Ulvaria obscura |
Acmeae testudinalis
Caprella spp.
Gammarid amphipods
Lacuna vincta
Margarites costalis
Margarites groenlandica
Mytilus edulis
Tonicella spp. |
Zone of Grazing-Resistant Algae |
Agarum cribrosum
Callophylis cristata
Clathromorphum spp.
Desmarestia viridis
Lithothamnion spp.
Phycodrys rubens
Ptilota serrata |
Acmeae testudinalis
Strongylocentrotus droebchiensis
Tonicella spp. |
Barren Zone |
Clathromorphum spp.
Desmarestia viridis
Lithothamnion spp. |
Acmeae testudinalis
Hiatella arctica
Strongylocentrotus droebchiensis
Tonicella spp. |
Zone of Filter Feeders |
Clathromorphum spp.
Lithothamnion spp.
Peyssonnelia rosenvingii |
Ascidia spp.
Boltenia ovifera
Chondractinia tuberculata
Cucumaria frondosa
Didendium candidum
Ectoprocts
Halocynthia pyriformis
Hydroids
Metridium senile
Ophiopholis aculeata
Psolus fabricii
Porifera
Strongylocentrotus droebachiensis
Tealia feline |
In Bonne
Bay, Newfoundland, sampling in 1990 of substrate at depths of 44 to 212
m indicated that annelids were the most abundant group in terms of both
abundance and biomass (Wieczorek and Hooper, 1995). The substrate at these
sampling locations was composed of fine sand, very fine sand, and silt/clay.
Two of these stations (South Arm and Wigwam Point) were less than 150
m deep and so the following is a discussion of these stations only as
they are most relevant to the depths found in St. Georges Bay (Table 13).
The annelids made up the greatest contribution to the faunal density,
comprising 43-66% of the total invertebrates (the sedentary polychaetes
formed 28.7-50% of total density), with crustaceans contributing 21.7-30%
and the molluscs from 9.8-21%. The remaining groups each contributed less
than 2% to the faunal density. Biogenic material (living and dead plant
material, mollusc shells, polychaete mucous tubes and casings, fish bones
and scales, and dead animal remains) made up by far the largest mass of
organic matter within the substrate (56.7-84.5% of total). In general,
the annelids contributed the greatest 'living' mass (12-20% of total)
with the cnidarians providing a large contribution at Wigwam Point (17%).
Contributions by the other groups to wet mass was variable between stations.
Table
13. Density and wet mass from sampling at two stations in Bonne Bay, Newfoundland,
1990. Note. Data has been converted to /m2, it is originally
reported as /13,000 g substrate (sampled with a 0.1 m2 Petersen
grab). Table adapted from Wieczorek and Hooper (1995).
|
South Arm
|
Wigwam Point
|
Depth (m)
Dominant particle Diameter
|
44-150
<0.062-0.25
|
68-126
<0.062-0.125
|
|
Density (/m2)
|
Wet Mass (g/m2)
|
Density (/m2)
|
Wet Mass (g/m2)
|
Mollusca
Bivalvia
Cerastoderma spp.
Small, thin shelled bivalvia
Gastropoda
Small gastropoda
Scaphopoda |
81
9
0
6
53
53
19
|
45
11
0
1
32
32
2
|
129
67
3
52
41
40
22
|
51
35
12
5
13
12
3
|
Annelida
Sedentary, burrowing and tubiculous Polychaeta
Errant surface dwelling Polychaeta
Errant burrowing Polychaeta |
542
411
53
2.8
|
732
551
109
5.5
|
267
176
24
26
|
343
238
42
45
|
Crustacea
Amphipoda
Small crustacea |
178
156
22
|
49
46
3
|
187
163
24
|
45
43
2
|
Echinodermata
Ophiuroidea
Asteroidea
Holothuroidea |
3
0
1
2
|
82
0
80
2
|
2
1
0
1
|
4
1
0
3
|
Cnidaria
Colonial Hydrozoa
Anthozoa
Porifera |
8
6
0
1
|
6
3
0
1
|
12
10
2
4
|
293
1
292
1
|
Other invertebrates |
9
|
31
|
4
|
8
|
Total invertebrates (/m2) |
820
|
|
613
|
|
Total mass (g/m2) |
|
6,105
|
|
1,725
|
Back
To Top
Summary
of Gulf of St. Lawrence
This
review of the benthos of the Gulf of St. Lawrence clearly indicates the
difference between the southern and northern Gulf. The results are summarized
below.
Based
on the limited sampling reported for the southern Gulf (five studies)
the bivalves, gastropods and polychaetes appear to be the dominant organisms
with up to 14 bivalve species, 9 gastropod species and 20 polychaete species
being reported within single studies. In terms of biomass, bivalves appear
to contribute to a greater degree than gastropods, Polychaetes are variable,
ranging from the greatest contributor of biomass (Bourget and Messier,
1983) to the least of the three groups (Hughes and Thomas 1971b).
Seven
reported studies from the northern Gulf of St. Lawrence and the estuary
produce different results from the southern Gulf. Crustaceans are a more
significant component of the presence, being in greater abundance than
molluscs and echinoderms in one study. Individual species appear to dominate
the benthos to a greater degree in the northern Gulf (e.g., Buccinum
undatum, Strongylocentrotus drobachiensis, Yoldia myalis, Asteria
sp.). Polychaetes, however, continue to contribute significantly to the
benthic community in the northern Gulf of St. Lawrence.
Perhaps
the greatest contrast between the southern and northern Gulf is in the
'Dominant' species collected (i.e., most commonly encountered or abundant
per capture event). See Table 14 for species comparison. As may be readily
seen, the benthic composition of the two areas are significantly different.
The number of common species per phyla/class for the most common groups
range from 8-10 for bivalves, 7-11 for gastropods, 1-11 for polychaetes,
and 2-10 for echinoderms. Decapod crustaceans are conspicuously absent
from this list.
Table
14. Listing of 'dominant' species reported from the southern and northern
Gulf of St. Lawrence. Absence of species from the table does not imply
that it is absent, only that it is present at lower density/abundance
than more dominant species. (e.g., Buccinum is present in southern
Gulf, but not commonly reported as abundant or dominant species). Table
compiled from studies reviewed herein.
|
Southern Gulf
|
Northern Gulf
|
Bivalvia |
Clinocardium ciliatum
Cumingia tellunoides
Gemma gemma
Macoma balthica
Modiolus demissus
Mya arenia
Mytilus edulis
Serripes groenlandica
Spisula polynyma
Tellina agilis |
Chlamys islandica
Clinocardium ciliatum
Hiatella arctica
Mya truncata
Mytilus edulis
Serripes groenlandica
Spisula polynyma
Yoldia myalis |
Gastropoda |
Cingula aculeus
Crepidula fornicata
Crepidula plana
Hydrobia minuta
Littorina littorea
Littorina saxitalis
Lunatia heros
Nassarius obsoletus
Nassarius trivittatus
Odostomia sp.
Retusa canaliculata |
Acmae testudinalis
Aporrhais occidentalis
Buccinum undatum
Lacuna vincta
Littorina sp.
Margarites sp.
Neptunea despecta |
Polychaeta |
Clymenella torquata
Gattyana cirrosa
Harmothoe extenuata
Harmothoe imbricata
Lepidonotus squamatus
Nereis succina
Nereis virens
Notomastus laticerus
Pectinaria gouldii
Polycirrus eximius
Scalopolos fragilis |
Pectinarea granulata |
Echinodermata |
Asterias vulgaris
Ophiuri sarsi |
Asteria vulgaris
Crossaster papposus
Cucumaria frondosa
Echinarachinus parma
Gorgonocephala arctica
Leptastarias polaris
Ophiopholis aculatea
Psolus fabricii
Solaster endeca
Strongylocentrotus drobachiensis |
Total Species |
34
|
26
|
Number of Species in Common |
6
|
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