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International Council for the Exploration of the Sea

C. M. 1959 Specia~ ~~fcMe e ting

"Some remarks on the distribution of zooplankton, fish eggs and larvae in the

~orwegian Sea in 1958 ~I

\

f Inves.tigations carried OUI; by the Ins tituce of Marine Res earch, Bergen, Norwa)T~

By

Kr. Fr. Wiborg.

During the year 1958 vertical Nansen net (118/7011) hauls from bottom to surface and.50 to 0 m, were taken regularly at the permanent hydrographica1. stations along the coast of Norway and Spitsbergen

(Sognesjgen, Sln-ova, Skarsvag, Kongsfjord (Kings Bay)), and during the first half of the year at the weathership station "Mf! (Fig, 1). At station liMit half hour's horizontal b.auls Were also taken weekly with a one metre net at the surface.

During the cruis e of R/S IIJohan Hjort" in the Norwegian Sea and the northern North Sea, from 28. April to 24. June, vertical hauls 100 to 0 m were taken with a one metre egg net (meSh size 0.5 mm) on 229 stations, and horizontal hauls with a high speed net on 43 stations (Fig. 2).

'rhe high speed net, a Gulf III model (Gehringer 1952) without nose -piece and current meter, was towed for 25 minutes at a speed of 8 knots in steps with varying wire length (125 ~ 25 m wire).

I. Zooplankton.

~!t~_ ~~::~~ti:?~~ J~_ ~~~~r;:~_ ~~. !~::: _~~(?J~l~.?l<!~~ ~~~rj~£t! 2~~

_c:

t_ ~l~e_ P~!!l2~::~::~

hydrographical stations and at station "M".

----~--~---~---~---.

At Sognesjgen plankton was sampled in March, April,

September, October and December. During these months the plankton was very sparse with a maximum mean value of 2.5 ml per haul in April.

A single Salpa fusiformis was taken in the middle of September.

At Skrova plankton was collected frequently throughout the year.

Fig. 3 is based on the monthly means, The winter minimum occurs in March.

There are peaks in May and July. The plankton was on the Whole more abundant than in 1957, especially in the upper layers, the spring and summer maxima being more pronounced and occurring earlier in 1958.

As in 1955, large numbers of Salpa fusiformis were taken throughout October.

At Skarsv§.g plankton was sampled from the end of June to November (Fig. 4). As in 1957 there were peaks in July and September but the plankton was more abundant than in the previous year.

At Kongsfjord (Kings Bay) a fairly representative material was collected from April to September (Fig. 5). The volume curve has a minimum in February, and two peaks, one smaller in June, and a main peak in August.

During the last half of September there was also some increase. In the upper 50 m peaks occurred both in July and August, and the September increase is more pronounced. The plankton was richer than in the previous year, and, as usual, Calanus finmarchicus cons tituted the bulk of the plankton.

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At station "Mlt plankton wao sa.m.pled from J2.iJ.uary to the eDd of June, During the 1aot half of the year the Norwegicm weathership8 were stationed at st, "All in the Denmark Strail.:. The pla.nkton rnc.terial collected at trAil, has been handed over to the Dcmiflh Plankton laboratory.

In the table below are given the monthly mean volumes in the upper 600 m at st. "MIt (in ml):

Haul Jan, Fe b1'. M8.1'ch Ap1'U M2.y June

25 - 0 m 100 - 0 m 600 - 100 m

<0.5

< 0.5 3.5

<

0.5

<0,5 0.5

0.5 L3

0,7 1,7

2.4 4.1 4,0

2.0 2.7 7.0 As in previous years: a maximum in volv.me in the upper 100 m was observed in May, but t1w plankton "waG 168 s abundnnt than in 1957. In daytime the horizontal surface haulG yielded BP.W.n quantit:06 of plankton, except for one haul of 180 ml at the G:'1.d of Vlay. The deht h2.u1s were richer, with a maximum mean value of 127 ml in April.. N'o night hauls were taken in January and March. '

'!'~~_ g~<:~~i!~tiy~_ ~~s_t!i~~ti..?!l_ ~f ~..?.?.pl<:1}~~c:r: i~ _t?~

_

~?!:~e..@~!1_~~~ _c!..~r}!llt ~c:.~-_

June 1958 compared with simultaneous echo recordings.

---

The plankton materie.l collected in May-June 1958 during the cruise of

Rls

"Johan Hjort tr in the Norvvegian Sea can only give a rough picture of the quantitative distribution (Fig, 6), as various errors are involved in the sampling, one of the major oneS being the variation in plankton volume between day and night hauls. In the northWestern cold area the plankton was fairly

abundant, mainly consisting of Calanus hyperboreus. In the central area the plankton was sparser, but the Norwegian (coastal ana bank areas were again richer. The dominating species was Calanus finmarchicus, but in some places euphausiids (kri11), fish fry, and m.eausae~played-an lmportant part. As was to be e~cpected, the largest quantities of plankton were taken during night time.

When echo sounders are operated in coasta.1 or oceanic areas, a shallow scattering layer, giving diffused echoes, may be recorded continuously for hundreds of miles, especially during the spring-autumn period. The recordings may vary both with respect to intensity and depth, but are usually limited to the upper 30-50 metres. Such a scattering layer has sometimes been identified as echoes of small fish, but the operators are of the opinion that the usual zooplankton organisms, copepods, euphausiids and others may also be important as sound scatterers.

In order to investigate if echo sounders can give a quantitative picture of the horizontal distribution of zooplankton, a special SIMRAD machine, producing signals of 27 kc, was run continuously during the whole cruise of the IIJohan Hjort". Each half-hour the operator noted the average vertical extent of the recordings (e,g. 10-50 m, 5-25 m) and made estimates of the intensity on a subjective scale from 1 to 6. The chg.rt which was prepared from these recordings (Fig. 7) does not agree very well wHh the quantitative distribution of plankton as revealed by the volume mea::;urements (Fig. 6). Particularly in the northwestern area, where the echo survey was entirely negative, no

agreement is found.

The borders of zero recording nearly follow the 30 - 40 isotherms at the 20 m level. In the central area, there is a certain agreement between small plankton volumes and echo recordings of low intensity, but in the eastern part the maximum of recordings does not coincide with the area of maximum plankton volumes.

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It thus seems, as if the echo sounder used cannot give a reliable pich1l"e of the quantitative distribution of the zooplankton. According to Fraser (1957), Calanus finmarchicus and salps are ineffective as sound reflectors for the echoco~ln;:rers"used on board the Scottish research ship "Scotia".

In order to find out which organisms were possibly responsible of be echo recordings, all the species present in the plankton samples were listed. Five groups of organisms were selected because of their size, namely appendicularians, chaetognaths, krill, fish fry and medusae. The chaetognaths occu:rred on nearly all stations, and no correlation could therefore be found with ~he echo recordings. In the remaining four groups the following relations were found:

1\;0, of stations ','rH-hout recording

68

~~ !l:~

.c:.::.e..c:.

s• ~i !~~':t ~:::y_

:

~ ~~:~~~g-=_

No. of stations with catches of:

;

Appendi - Krill cularians

4 25+)

Fish Fry

2+)

Medusae Nil

o

40

+)

SineJe specimens only.

~r:. !~~

_c::r..e..c:.

s_ ~i!~ _:r..e..<:~:r..c!,i!lS_ <?~ ~lp~<:~l:t'?~t~:_

No. of stations with catches of:

No, of sta.tions

with recording Appendi-

Krill Fish

Medusae Nil

cularians Fry

157

65

111 85 41 5

Krill, fish fry and medusae did not occur in the "negative" area, except as single specimens. In the "positive" area only 20 of the stations yielded merely appendicularians andlor medusae. On the remaining stations krill and fish fry were also present.

In the areas with maximum of echo recordings krill and fish fry were taken on all stations, partly in large numbers.

It seems as if the recording of "plankton" may in general be referred to the organisms mentioned above, chiefly krill and fish fry. In a few cas eo small squid have been caught, and it is likely that they also play a certain part as sound scatterers. Usually very few squids are caught in the plankton nets, and the operators are of the opinion that the echoes caused by s quid may be dis tinguished from other echo signals.

The horizontal distribution of the various copepodUe stages of Calanus

---~--- ---

finmar chi cus •

The plankton nets used were of silk No. 0 (mesh size 0.5 mm), therefore nauplii and the copepodite stages I of Ca1anus finmarchicus were not caught in quantitative numbers (Wiborg 1948). It may nevertheless be of some interest to compare the stage distribution of Calanus finmarchicus in the various areas. According to Pavstikhs (1956) the biological spring occurs at different times in the various parts of the Norwegian Sea, in March-April along the western and northwestern coasts of Norway, in May-June in the central area, and in July-August in the western and northwestern areas •

. I.

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The average stage distribution of Calanus fim~archi~u~ is shown in Fig. 8. In the southeastern area the

sprrng

spawnln~rv;"asprobably completed before the cruise started, and the copepodite stages III"IV present belonged to the spring generation. At some distance from the coast there is a wedge with predominance of the stages V" VI, evidently related to warmer water of the North Atlantic current (Fig. 9). Different wedgeshaped areas with predominance of stages IV - V (4.0 - 4.5) can be followed northwards.

As the obs ervations were made during a period of more than

li

month, the material does not justify a very detailed synoptic description.

The isopleths usually follow the isotherms quite closely at the 20 m level (Fig.

9),

and the attention is drawn to the isopleths in the sections from Bear Island to the west and south, and to the tongue of stages V-VI (5.5) running north and northeast at approximately 50 W.

The stage distribution of Calanus finmarchicu8 may thus be used supplementary to the hydrographical observations in order to distinguish the various water masses in the Norwegian Sea,

lI. Fish eggs and larvae.

The plankton material collected at the Skrova station (Fig. 1) since 1949 has proved very useful in the study of the spawning and develop- ment of eggs and larvae of the arcto-Norwegian stock of cod (skrei) in this area (Wiborg 1957). The variation in number of cod eggs and larvae at Skrova during 1958 is shown in Fig. 10. In February a few eggs were present, in March the number increas ed to a maximum of more than 1200 per haul, and decreas ed throughout the following two months to zero at the end of May. The cod larvae appeared at the beginning of April with greatest abundance at the end of this month and in the middle of May. Later in the seas on the larvae probably avoided the Nansen net. Cod eggs and larvae were much more abundant than in 1957.

The size distribution of cod eggs in various years has been studied at Skrova (Fig. 11). A small, but obvious decrease in the mean size from the beginning to the end of each season was observed, especially in

1951 and 1957, but rather inconspicious in 1956, The variations in egg size are assumed to be related to the size of the fish. In some fishes, e. g. the char (Salvelinu8 alpinus the larger females produce larger eggs than the smaller ones Aass 1951 , It is generally known that in the Lofoten area the larger skrei usually arrive first at the spawning places, and the smaller fish at the end of the season (Sund 1938),

A similar variation in the mean size has also been observed in haddock eggs at the weathership station "MI! in the Norwegian Sea. In 1958 some eggs of haddock Were taken at station "M" from 11. April to

13. May, mainly in surface hauls with a one metre net. The size distribution of 84 eggs sampled 25. April is given below:

55 56 57 58 59 60 61 62 eye -piece units 3 3 11 11 23 16 10 3

Mean size 58.9 un.

=

1.47 mm.

In 1954 the mean size was nearly the same (58.8 un.) and well above that of 1955 (56.8 un.

=

1.42 mm) and 1956 (57.3 un.

=

1.43 mm).

Newly spawned eggs of cod and haddock are very difficult to

disting~ish, and differences in the size distributions of the eggs have been / used wlth some success (Saville 1956). However, such differences should be used with care, as annual or seasonal variations in egg size within the same species, such as those referred to above might invalidate the method,

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The cruise of the IIJohan Hjort" to the Norwegian Sea was not planned specially for investigation of fish eggs ahd larvae. The observations in coastal waters are few and the dispersal in time is great, nearly two

months. The material has, nevertheles s, given much valuable information on the distribution of eggs and larvae of various spec:l.es of commercial fish.

_ Cod. (Fig. 12). At the end of May vertical hauls yielded cod larvae oh sonie-oT'fhe stations off Lofoten and Vestel'dlen with a maximum of 27 specimens per haul) and a few larvae

on

the baiiks farther northeas t4 In the period 17. -24. JUli~ some cod fry, 10 to 30 mm in length; were taken in the same area with

a.

high speed net (Table

I).

Table 1. Number and length distribution of cod fry taken in high speed net (125 -25 m wire length), 25 minutes, speed 8 knots 17. -24. June

1958 off northwes tern and northern Norway.

_ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ M P _ _

Area No, per

station Length, mm

8-12 13-17 18-221:3-27 28-32 33-37

Mean length

---~-.--- ----._---

Tromscp-

flaket- 18 11 17 8 19.8

North Cape Andenes-

55 2 25 53 24 6 1 20.4

Eggum

Off Eggum 32 2 12 46 54 38 10 24.5

It is noticed that the largest cod fry taken, off Eggum, had a mean length of 24.5 mm.

Haddock. {Fig. 13}. Eggs and larvae of haddock occurred in two main areas. On the Viking Bank and east of Shetland, up to 75 eggs and 11 larvae per vertical h'aul were taken at the end of April. A few larvae and eggs were caught on the Halten Bank and along the edge of the continental shelf. The other main area was situated off Vester&len. Single haddock larvae were taken in the open ocean very far off shore. This conforms with the

occurrence of haddock eggs in the same area in earlier years. -

Most of the larvae measured 5-11 mm, single specimens as much as 18 mm. During the last half of June small haddock, measuring 26-46 mm, in length, were caught in the high speed net off VesteriHen.

According to earlier Russian and Norwegian investigations, the spawning areaof the Barents Sea haddock is situated along the edge of the continental shelf from Scprcpy to 650 N., with the centre off Andenes and Vester&len. The eggs and larvae may remain for some time in the anti- clockwise eddies situated off the edge, but are gradually transported north- and northeastwards. In July-August the young haddock are dispersed over a wide area, but mainly north of 70° N.

Saithe. (Fig. 14). A few eggs and larvae of saithe were taken at the end of April east of the Viking Bank, and in the first half of May off Stadt and on the Balten Bank. In June single young saithe, 17 -45 mm of length, were caught with the high speed net on the coastal banks between Scprcpy and

Lofoten.

Tusk. (Fig. 15). Eggs of tusk were mainly found within the 400 m contour with a maximum of 15 eggs per vertical haul (20 pr m 2). In May, single newly hatched larvae were taken on the Halten Bank. According to earlier investigations the tusk also spawn in the deep of the Norwgian fjords •

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Her!ing, (Fig, 16). At the end of April, herring larvae were numerous on two stations northeast of Shetland. The length distribution was as follows ~

9 1

10 1

11 8

12 6

13 15

14 14

15 15

16 6

17 1

18 mm 2

M-ean length 13,7 mm

At the beginning of May herring larvae were also taken off Stadt and near the Balten Bank, with a maximum of 28 specimens per haul.

The mean length of the larvae decreased from 19 mm to 12 mm in a sedion from the bank towards the coast,

Only single herring larvae were caught on the banks north- east of Vestera1en, and observations are assumed to be taken too late in the season to trace the spawning in this area.

From the end of May to the last half of June fairly large numbers of herring fry were caught in the high speed net (Table 2).

Table 2. Number and length dis tribution of herring fry taken with high speed net (125- 25 m wire length, 25 minutes, speed 8 knots) in various areas along the

________

~.?!~~~i~!l_ ~~~~t

3l.:

lv!~¥ _-_~.:. !~!!!!_ <;~~

}}_,_

-_~4:.._~,:r:.~} J2~.!_

tS_e;.e..

!.~.~.:

_

!~t,

__

~ ~

__ _

Area

Off Lofoten- Vesteralen

31. V-6. VI (Bear Isl.)-

Fugl1Jy- N. Cape N. Cape-

Lofoten Lofoten-

M1Jre

St. 445

L th ' Mean Average no.

eng· ln mm . . . . :

13-17 18-22 23-27 28-32 33-37 38-42 43-47 48-52 length per stat ... on mm

2 18 38 15 1 25.2 12

24 112 18 2 25,2 25

8 46 95 36 2 24.4 31

15 93 54 10 2 27,0 17

1 12 16 4 430 4

With the e,,;ception of one sample (st. 445) the herring usually varied in length from 13 mm to 42 mm, and the mean lengths from 24.4 mm to 27.0 mm. The smaller larvae were taken close to the coast, the larger ones farther out at sea.

One haul taken at the edge (Fig. 16, st, 445) yielded herring

fry 37 -49 mm of length, mean size 43.4 mm. These herring may have originated from an earlier spawning than the bulk of the fry taken, either off Mrpre, or

they have drifted with the currents from the Faroe area. The herring fry taken off M1Jre on 24. June, were however, much smaller, with a mean length of 25.6 mm.

Redfish. (Fig. 17). Fry of redfish were chiefly taken in the vertical hauls between the edge of the continental shelf and the central part of the Norwegian Sea. The boundary of the distribution towards the west agrees very well with the 40 C isotherms at the 20 m level. (Fig. 9), and also with the limits given by Baranenkova et .. al. (1957). Off Andenes redfish larvae numbered up to 137 per haul, and the larvae were also numerous farther north, outside the 1000 m contour. At all stations the length distribution was quite. /.

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narrow, from 7 to 13 mm with a mean length of 9.4 mm. Most of the larvae measured 8 -11 mm.

In the middle of June redfish fry were numerous in the high speed net hauls between Bear Island and North Cape, with the following length dis tri bution:

7 1

8 ,. 9:' la·. 11 1 8 25 51

12 55

13 33

14- 15 mm 12 5

Mean length 11. 7 mm

A few larvae caught simultaneously in vertical hauls with a one metre net measured 9 .. i2 mm, mean length 10.2 mm. West of Bear Island three small redfish, measuring 12,.24 and 27 mm respectively, were caught on 13. June.

For a study of the growth of the redfish it might be of interest to compare these data with the length distribution of small redfish taken from the stomachs of cod and haddock of the a-group, caught with purse seine

30~July 1957, ~20 ri. miles to the northwest of Andenes:

7

8 9 1 0 11 12 13 14 15 16 1 7 18 1 9 mm

1 2 4: la 11 17 8 4 3 2 1 1 1

Mean length

11.9

mm At Syltefjord on the Varanger peninsula, North Norway, some young redfish were taken with the high speed net 4. August 1955. They

measured as follows:

12

1

13

o

14

o

15 1 16 3 17 3 18 3 19 5 20 5 21 2 2 2 1 22 23 24 25 3 26 0

Mean length 19.8 mm

27 mm

1

Taning (1949) gives a mean length of 12-14 mm of redfish fry taken in the North-Atlantic in June -July.

Summary.

During 1958, zooplankton was collected at 4 permanent

stations along the Norwegian and Spitsbergen coasts, and at the weathership station "MU (Fig. 1). Peaks in plankton volume occurred in May and July at Skrova, in July and September at Skarsvag and at Kongsfjord, Spitsb ergen.

The plankton was more abundant than in the previous year, except at station liMit.

Salps occurred at Sognesjst>en in September, and at Skrova and Skarsvag in October.

The spawning of cod has been followed at Skrova during the spring of 1958. - The peak of spawning occurred in the middle of March.

There appears to be a general decrease in the mean egg size during the spawning season in the various years, correlated with the size of the fish. The same feature has been obs erved in haddock eggs from station liMit.

Zooplankton and fish fry were sampled during a cruise in the Norwegian Sea in April-June 1958. An echo sounder was run continuously during the cruise in order to record the zooplankton. The records did not agree with the quantitative distribution of plankton and the sound scattering is assumed to he caused mainly by euphausiids, fish fry, small squid and medusae.

~ larvae were mainly found in the Lofoten- Vesteralen area.

Eggs and larvae of haddock occurred on the Viking Bank, the Halten Bank and off the edge outside Lofoten and Vesteralen. The latter

area is supposed to be the main spawning area of the Barents Sea haddock .. /.

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,.,

SaHl1e larvae and eegs were taken on the Vildng I::,an);, and :Halten Bank,

fa:J:'g0i'-iry

farther n,)rth.

':CusIc eggs)ccurrec. mainly within the 400 m cont:)ur from the l\T::fl!'thern N0-:r~h Eea to Vesteri11en.

;:':ie):ring larvae were i.)lenHful in A~)ril-May eas t of Shetland and on the Halten E,ank. -'-,arger he:c:dng fry were taken in June with the high

s~')eed net in the e;,;)astal a:teas from N)rthcape tJ Msore •

. ledfish larvae were numel',JUS in the'~::l£oten-,Andenes area, mainlY:Jfi ~he e~5ge'. :':_:arger fry were tah:en in June in the secti:m E:ear Is land ~Fugltpy.

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References.

Aass, P. 1951. Rognmengden hos rrpye. Norsk Jeger- og Fiskefor. tidsskr.

nr. 10.

Baranenkova, A.S., Khokhlina, N.S. and Judanov, I.G. 1956. Thedistri- bution of fry of redfish of the genus Sebastes in the Norwegian Sea. Dok!. Akad. Nauk. SSSR, Ill, No. 2 (in Russian).

Fraser, J.H. 1957. Scottish plankton investigations in 1955. Ann. BioI. 12, p. 44.

Gehringer, J. M. 1952. An all-metal plankton sampler (Model Gulf Ill). High Speed Plankton Samplers. SSR.}:!....,. No. 88, U,S. Fish &:

Wildlife SerVe Washington.

Pavstikhs, E,A. 1956. Seasonal variations in the plankton and the feeding migrations of the herring (in Russian) Trudy PINRO 9, pp 93-145.

Saville, A. 1956. Haddock eggs and larvae at Faroe. Scot. Home Dept., lVIar.Res. 1956, No. 4, pp 1-27.

Sund, O. 1938. The stock of cod in 1937. Fiskeridir. Skr. Ser. Havunders. 5, 7 pp 48-49.

Tc1ning, A. V. 1949. On the breeding places and abundance of the Red fish (Sebastes) in the North Atlantic, Journ. Cons. 16, (I), pp 85 -95.

Wiborg, K. F. 194:8. Experiments with the Clarke -Bumpus plankton sampler and with a plankton pump in the Lofoten area in northern Norway. Fiskeridir. Sler. Serf Havunders. 9, 2 pp 1-32.

Wiborg, K. F. 1957. Factors influencing the size of the year classes in the Arcto-Norwegian tribe of cod. Ibid. 11, 8, pp 1-24.

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68

I ,

641- I

60

-1,0-

--. -.. --,---r----.

ST.M·.

I

I

I~ __ .~ ___ .... _.· .. __

-L _ _ _ _ ---'--'

10 20 30

---~ _ _ _ _ _ _ ->-,. ---1----'

o 5 10 Ib 25 30

Fig. 1. Permanent zooplankton stations in Norwegian and Spitsbergen waters.

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200 10' 10'

7S

o

.---y---.---r--- ---.---__

~,-,----~r---~7S.,

,

• •

I • ••••

•••••

••••••

• • • • • • •

• ••••

• • • ~4I.4ItIv

I.

iEAR ISLAND I;

"":: ,

• • •

.!

.<

~

o

~~,

,.' 'f'

·e \

,+; I

I RIS "JOHAN HJORT" 28.IV • 24:\'1 1058 I

OD HIGH SPEED NET 125-25 MW

• • METER NET 100 -0 m

Fig. 2. Plankton stations in the Norwegian Sea April .. June

1958.

rnl

---_

... ,~' M

I I I I , I I

I

~",,)

#' f '

I '

I '

I I I

M

21.G

SKBOVA 195&

- 3 0 0 - 0

-- - SO-o

,_ ...

-

.... -...

_-

...

_-

s o N o

Fig. 3. Variations in plankton volume at Skrova. Monthly means.

Nansen net hauls.

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"".

20

18

4

IKAASVAO len

- aGO-Om

SO·O

23

'1 A

I I , I

, I

I I I I

I I

I \

I 1

\ I 1

\ I 1

\ I I

\ \ ___ .... " \ ,1

' .

,

" .

. _-

A $ 0 N 0

Fig, 4. Variations in plankton . volume at Skarsvdg,

June-November 1958.

Nansen net hat;lls

-12-

""

ICI

12

8

4

21

KONG SI'JOflD lOse _ _ 300-0

Fig.

--- ~o-o

,.

/1 1 1 1 1 1

1 , 11 11

r

o

5. Variations in plankton volume at Kongs£jord, February-October 1958. Small Nansen net, "8/50", and double figures.

2~ 10' ~ 10' 20'

15'r-~r---r---~r---~----~~---;~---~'7§'

PI.ANKTON VO\..UME5 28.IV - tS.VI 1958

'65' METER NET lOO-Om

...

< 10 ml

...

10-20 ..

"

20-40 ..

ttt:::t:l: 4(\-<10 ..

-

> ~O .,

I

eo·~----·--·---·-~---~---X-~---~~----L---. L --_...JOO·

2~ t~ 10' 20'

Fig.

6,

The quantitative distribution of zooplankton, April-June 1951}, one metre egg net, 100-0 m.

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'ZO· to" 0" IQ" 20"

75" .--.,...---r---~---_:_-~---+_---..;...-:;;;.---...:...,.,.,.

- - - - _0 __

-- - - -- -

-:~

-=:=:::~=~=:=::=:=~-

----

~---t

-:-::. -: -:':'\E-: -:-

~t

'

70. r---~--..",...--.!---_/_---""':-:-:-:-:

_

~: ~

--:-:-:-:-:-:--

-~,

-~---~---.

-

,;IJ J/l1II MAYEU'/

ECHO SURVEYS

OF' .. PI. ... NKTON ..

28.IV -18N' 105&

< 00 UNITS

~ __ . tl~_]....::l.iUr_~~tJ:!.'_:_l__. _~_'

9 ...

:".1...:'=_

'0" 2 .. 0-"---1":0~"- (y 10' 20' ---">'60'

Fig. 7. Echo surveys of "plankton" April-June 1958.

(14)

-14-

7 5 " . . - - . - - . - - - , - - - , - - -

i I

. _ . ____________ .. _-'L.-'-:-_ _

10·

2O,V-31,V

-- 10'

4V1·18V1

1 20"

Fig. S. The mean stage distribution of Calanus finmarchicus April-

June 1955. ---

(15)

200

lOO

40

20

10

4

-15-

7~r-~---~---.---.---~~---,---~

20,

t'e ,20';' 281\1" ~VI 1956

10" 10' 20'

Fig. 9. The isotherms in 20 m, April-June 1958.

MARCH

SKROVA 1058 ._COO EOOS

- - - coo LARVAf;

NANSI';N NET

f--

I \

,

\

,

~

, , , , ,

I J

'\ I

\ I

\ I

APRIL MAY

10. Number of cod eggs, and larvae in vertical Nans en net hauls at Skrova February-May 1958.

I'nm

I.~

1~$8

1.45

1.40

1956 n----o<..-

VARIATIONS IN THE MEAN DIAMETEA OF' COD EGGS SKROVA,LOl'OTEN AREA 11151-11156

1~5~---'--~---.---.---r--.---~~~--~

7. 15. 23. e. . 10. . 24. 2.

MARCH APRIL MAY

Fig. 11. Variations in the mean diameter of cod eggs at Skr ova during the period March-May in various years.

(16)

-16-

O' iO' 20·

I I

'000

\ .~:

0 0 0 0

\

\ \

()

I

10'~; ---~---~--_r---

I I

I I

"_ L ...

I

\ 1 1000 , .

o

o

COD LARVAE APRIL-JUNE 1958.

• MNET-O H.SNET

0 1-10 per HAUL

'8

11 - 25 "

26-50 "

\. > 50 "

20·

I .

"

"

"

Fig. 12. The quantitative distribution of cod larvae April-June

1958.

(17)

.'

I I I I I

I / I

-17-

o

e

'1---+----+---1---:-t-,~:__-

HALTEN

1000 I I

(

/ / / '

""

...

100'" . ) 1)'\" "

BAN/( •

SA.lTHE LARVAE APRIL-yUNE 1958.

• M.NET-O HoS. NET

• 0 1-10 per HAUL

,~---~---.-J,eo·

Fig. 14. The quantitative distribution ~f saithe larvae April':'June 1958.

(18)

~"

- - ,.

""

1000

I

~

/

I

t

\

, ••

.:o~-...,.

,,/too

L ____ ~-:_;~~{1._. _____ ~ ... ~

-18 -

TUSK EGGS APRIL- JUNE 1958 .

• M.NET

• 1-10 pe,.. HAUL '.11-25" 11

I

I

.---.. --' 1--.---:J

60-

200

Fig. 15. The quantitative distribution of tusk eggs April-June 1958,

(19)

10·

'/

V

I

• I I / I

I

65- I • HALTEN

\ SANK I

;..-/ tDOO ,-",,,,

,...-'-

-19-

.-

,

,

1000 \

\

\.

l

\

\

\

\

HADDOCK LARVAE APRIL-JUNE 1958.

• M. NET - 0 H.S. NET

. 0 HO per HAUL

• 1J-25 "

6~----~~---~~--~~---~60' O· . Fig. 13. The quantitative distribution of haddock larvae April-

June 1958.

(20)

-20-

20~

75- ---~~---r---"

-. -_ .. -- ._" -

.--,_.- ---,75·

I I

I

o

IlJ'

'J d£AR ISLAND o

65- ~---~---~~~~---+,~~-­

IHALTEN4

HERRING LARVAE

APRIL~JUNE 1958.

• M.NET -OHSNET ' BANK

I .' 0 1 - 10 per HAUL

0/ ...

" 00

:Y:J~.'

/ O.

rMIRE 1000 '" : ....

"

"

.-'..

./

" 4. SrA~r. ;.

'8

11-25" "

26-50 11 11

> 50 11

. . ___ ... ____ . _____ .. _ ... ___ 1 __ . __ . __ ._ .... __

20·

Fig. 16. The quantitative distribution .of herring larvae .. April-

June 1958. .

(21)

-21-

75·1---,---~---~---~~---T~---~75· 20·

,.."

(

I I

.1 I I

, ,

\

70·

70·

• • ••

0

• •

0 ,

0 ' f

0'

• ( /

,

~65'

.. I I

R~FISH

LARVAE

~5· A RIL-JUNE 1958,

I ., MNET-O H.S. NET

I

0 1 -10 pe-I" HAUL

I

.,

0 11 - 25 " It

(

.0

2.6-50

I It

, eo>

"

50 11 "

1000 . . , /

...

....

I

iO·

.J_ ...•.. -~60.

I 0" 10· 20·

Fig. 17. The quantitative distribution of redfish larvae April- June 1958.

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