• 検索結果がありません。

鹿児島大学リポジトリ

N/A
N/A
Protected

Academic year: 2021

シェア "鹿児島大学リポジトリ"

Copied!
7
0
0

読み込み中.... (全文を見る)

全文

(1)

New Data on the Daily Migration of Planktic

Foraminifera near the Island of Amami-Ooshima

Akio Hatta*, Kiyoshi Shimada*, Masataka Higashf

Akimasa Habano**, and Takafumi Azuma

(Received October 15, 1998)

abstract

The daily migration of planktic foraminifera was investigated off the island of

● ●

Amami-Ooshima, in the Nansei Islands, in the West Pacific Ocean. In order to clarify

the daily migration of planktic foraminifera, samples were collected at the same

loca-●

tion by positioning ship at the same latitude and longitude with the GPS (Global Posi-tioning System). Planktic foraminifera were collected by vertical towing at depths of 0 to 200m, which were divided into 4 zones.

Introduction

The distribution of planktic foraminifera in the West Pacific Ocean was investi-gated by Hatta et al. (1990, 1992, 1996). The main purpose of these studies was to survey the ecology and environment of living planktic foraminifera. As the studies clar-ify the distribution, a new question arose. The question is the daily vertical migration

of planktic foraminifera appears to be the reverse of that of other small planktic am-mal, which exist in the deep zone in the daytime and in the shallow zone in the

night-●

time.

In order to clarify the question, the daily migration of planktic foraminifera was

investigated off the island of Amami-Ooshima in the Nansei Islands in the West Pa-

cific Ocean.

Previous works

B丘(1977) studied the planktic foraminifera from the ecological and zoogeographical point of view. He observed that the highest concentration is generally found below the

surface, approximately at depths of lOm to 50m, and some species live in the sunlit

* Faculty of Education, Kagoshima University, Kagoshima, Japan * * Faculty of Fisheries, Kagoshima University, Kagoshima, Japan

(2)

waters for the maintenance of their symbiotic zooxanthellae, and the olive-green or brownish color of the protoplasm in epipelagic individuals is indicative of either freshly

●      ● ●

ingested phytoplankton or the presence of symbionts, and no other species except Hastト gennella digitata are known to spend their entire life cycle below a depth of lOOOm.

He stated that many species spend their earlier stages in the epipelagic zone and

even-● even-●

tually seek deeper habitats. With regard to daily vertical migration, he explained that

many nekton and plankton groups migrate upward at dusk, presumably to feed in the relatively rich surface waters, and usually descend to deeper levels before daybreak. This widely observed phenomenon of daily vertical migration has prompted a number

of investigators to determine whether a similar relationship exists for planktic

fora-● minifera. r r ○ 12 9 ▼ E 1 ーK o d a k a ra -一●im a Is .■ ○ 3 0 -I S a m p lin g s ta tio n も T a k a ra -一●im a Is .■ ○ A m a m i-O o s h im a Is . Q K ik a i-jim a 一S ■

(3)

According to B丘(1977), Rhumbler stated in 1911 that planktic foramimfera were more abundant in the daytime than in the nighttime at depths above 200m of the

wa-●

ter column. This trend is completely the opposite of the diurnal pattern of the migra-tion of most planktic and nektonic organisms. On the other hand, Boltovskoy menmigra-tioned

in 1973 that he did not observe any daily vertical migration in the planktonic

fora-●

minifera collected with a pump in the South Atlantic surface waters at depths of Om

to 5m between Argentina and South Africa.

Hemleben et al. (1989) asserted that vertical migrations may also occur and are reported at several locations, and the pattern of these migrations appears to be

comph-●

cated and is not fully understood.

Table 1. Time, position, drift and wind during sampling Lat. N29-  Long. E1 30-  Direction Knot Wind

21 :30     9.89     30.40 22:00 22:30      8.97     31.61 23:00      8.40     32.21 23:30 1 :00      9.58     30.62 1:30     9.20 2:00      1.99 2:30 3:00     8.61    33.46 3:34 4:00     10.08     30.57 4:30    10.03 5:00    10.02     31.97 5:30    10.01    32.70 6:00    10.04     33.46 6:30 7:00      9.98 7:30      9.98     31.74 8:00      9.97 8:30 9:00 O O O O O t D O O O O O O O O O O   0   -  0   0   0   0   0   0 0   m o m r o o c o o m t t O m o m o ア       ei <r> o o [ ・ "   「 L   ∵ L   . "   H . ー   L i i H h ド r                               「                               b T M u こ   ち て 1 0.02     30.07 9 77     31.08 9.45 9   8   8 1 5     33.46 76 44     35.72 10.08 9   9 80 50     31.87 1  7 3   0 9   9 8   9 32.90 33.95 82     34.75 96 1  7 3   7 9 00 e n e r >     c o t ^ . 31.14 32.07 35     33.02 98     33.96 87     34.38 97     30.08 24 47     32.00 61     32.96 33.93 15 N Ifl (M O      」 4 OT CM r^ co o m m oo cr 2   3   3   2   3   2   0   0   0 1  1      -  1   1  1  1 -    蝣 ォ   i d i n c m t -  * "   o o i s . G) G) CTi O* CO n m N o m O O in co id r^ ⊂J O 9 」 3 )   ( J )   ( J )   C T   ( J l o o o   ォ ー   o l 1 1 l 1 O I D   ( f l t A 「   5   2   7 L O to r- it (ji m m w * n 1   0   o o o r s i r v i   -  -  0 1  1  1   -       -  1 6   5   4   4   3 c t >   m t n o c o (¥j m m  ォ  tn 1 1 1 1 1 *   *   i c   < c   ^ r r r   ( ¥ j 1 l I I 1 l       1     1     1 O   < ¥ J   < ¥ J C M   ^ * " 1 1 I 1 I t o v   * r   < * 蝣   v c 1 1 I l       ▲ 一 C O C ¥ J C V J f ¥ J O I N M     ( M N U) CO 00 CO r -    ォ ー     サ ー     C ¥ J O O 0 0 O O f ¥ l CsJ f¥l r- r- fSJ rg eg v cj l M M     ( ¥ l M I M NEZ N3 N3 N3 N4 N3 N3 N3 ヽ N2 NNW 3 NNW 2 NW3 甘WE NW3 NW4 NNW4 T j -        t j -                    r r         -< 3 -        * S S             ァ       S     ァ z Z z Z   州

(4)

Sampling method and materials

The sampling station is shown in Figure 1. Planktic foraminiferal samples were taken from the point of lat. 29 10'N, long. 130- 30'E near Amami-Ooshima. Sampling

was executed from 21:22 on September 1 to 19:40 on September 2, 1997. Detailed time,

∫ ∫

sampling position, dri氏and wind direction during sampling are shown in Table 1.

Samples were collected at the same point for 8 times at intervals of 3 hours in one

day by positioning the ship at the same latitude and longitude with the GPS(Global Po-sitioning System).

Table 2. Sample number, start time, start position, inclination of wire, added length of wire, final time and final position near Amami-Ooshima on September 1-2, 1997 S am p le num ber 1 2 3 4 5 6 7 8 S tarttim e 21 ‥22 0:25 3:34 6 :32 9:33 12 ‥34 15 :29 18:3 1 S tart position N 2 9. 10 .0 0 1ー 10 .03 5ー10 .09 9ー10 .07 8ー10 .07 2ー10 .08 7ー0 9 .97 7ー09 .96 0ー E 130. 30 .237 ー29 .95 0ー30 .01 6ー30 .14 8' 30 .08 5ー30 .00 2ー3 0 .20 9ー30 .13 4ー Inclination of w ire at a depth of 200m 2 0 220 2 00 3 1ー 34 0 2 80 4 50 4 80 A dded length of w ire

at a depth of 200m

0m 15m 13m 33m 4 1m 26m 80m 90m Inclination of w ire at

a depth of 150m

6 0 290 2 20 140 34 0 3 00 3 80 44 0 A dded length of w ire

at a depth o f 150m 1m 25m 12m 14m 3 1m 23m 40m 59m Inclination of w ire at

a depth of 100m

4 0 210 2 40 12 0 32 0 24 0 32 0 40 0 A dded len gth of w ire

at a depth o f lO Om

0m 7m 9m 2m 18m 9m 18m 3 1m

In clination of w ire at a depth of 50m

00 120 13 0 2 0 200 280 320 340 A dded length of w ire

at a depth of 50m 0m 1m 1m ー0m 3m 6m 9m 10m F inaltim e 22:27 1:26 4:31 7:30 10 :3 9 13:33 16 :3 9 19 :4 1 F inal position N 2 9. 09 .0 0 1ー09 .229 ー10.0 45ー0 9 .9 8 1' 09 .3 59 ー09 .47 6- 08 .66 6ー08 .140ー E 13 0. 3 1.5 65 ー31 .222 ー3 1.3 34' 31 .7 76 ー32 .6 58- 3 1.97 81 32 .36 3ー32 .34 6ー 130-30       130-3 1      1 30-32 Longitude

(5)

Sample number, start time and position of sampling, inclination of wire, added length of wire, and final time and position are shown in Table 2. The locus of ship

move during sampling is shown in fig.2. The ship drifted approximately from North-west to Southeast.

Planktic foraminifera were collected by vertical towing at depths of 0 to 200m

which were divided into 4 zones, 0-50m, 50-100m, 100-150m, and 150-200m. Table 3. Planktic Foramimfera at sampling station

Sam ple N o.

D epth

8

150 -2 00

37

49

6 1 12 2

95 1 10 10 4 250

100 -15 0

8

34

8 0

6 1 136

8 1

69 149

50-100

39

69

4 3

96 365 18 5

69 196

0-5 0 m

39

53

73

79 140 146

94 220

T ota

123 205

25 7 35 8 736 522 33 6 8 15

A d ult)

Sam ple N o.

D epth

8

150 -2 00

6

3 7

100 -150

12

10

27

6

34

50-10 0 、

11

50 134

46

11

56

0-50

0

3 5

10

36

66

20

T ota

13

6 4

79 201 1 18

43 136

Y oung)

Sam ple No .

D epth

8

150 -2 00

9

10

3

16

25

15

8

20

100 -150

5

10

18

4

13

5 0-10 0

6

10

9

13

43

23

2

24

0 -5 0

14

39

59

21

22

30

T ota

24

3 1

3 1

78 14 5

64

36

87

(JuVen

Sam ple No.

D epth

8

150 -2 00

28

35

52

97

66

9 4

90 19 3

100 -150

2

24

63

4 1

9 1

71

59 10 2

5 0-100

32

57

23

33 188 116

56 1 16

0 -50 (m )

32

4 5

24

30

45

59

52 18 1

Tota

94 16 1

162 20 1 390 340 25 7 592

(6)

Features of the number of planktic forammifera

The collected foraminiferal samples were first divided into adult, young and juve-nile groups. The number of planktic foraminifera at the sampling station is shown in Table 3. The lowest total number of the collected foraminifera is 123 of sample No.l, and the highest is 815 0f sample No. 8.

The number of the collected foraminifera is low in the nighttime and rises in the daytime. Figure 3 shows the frequency of the whole, adult, young, and juvenile

● planktic foraminifera. 「 上∴票3(m) 100 -150 -200 l

l L三岳超塁.

】 0     0   0   0 5   0   5 r i i i Young 1   2    3    4    5    6    7    8

(7)

Discussion and prospect

The difference of the total number of the collected planktic foraminifera between nighttime and daytime may be explained by either the variation of capture quantity

be-●      ● ● ●

ing prominent became of patchy distribution or nocturnal migration below depths of 200m. However, the gradual increase of number from night to daytime suggests that

nocturnal migration is a more likely cause. The length of added wire indicates that the planktic foraminifera of sample No.8 were collected from depths deeper than 200m.

To confirm this hypothesis, we must collect planktic foraminiferal samples from greater depths.

Acknowledgement

We express our gratitude to Associate Professor Toru Aoyama of Kagoshima

Uni-●

versity Research Center for the Pacific Islands for his reading of the first draft.

References

B丘, Allan. W. H. (1977): An ecological, zoogeographic and taxonomic review of Recent planktonic

Foraminifera. Oceanic micropalaeontology, (ed. Ramsay, A. T. S.), Vol.1, p.l - 100. Academic Press, London, New York & San Francisco.

Hemleben, Chnstoph, Michael Spindler, and O. Roger Anderson (1989): Vertical distribution ; Patchi-ness and daily vertical migration, in Modern Planktonic Foraminifera, p.235-239, Springer-verlag. Hatta Akio, Yasutaka Yuwaki, Toru Nishi, Sunao Masumitsu, and Masataka Higashi (1990):

Plank-tonic Foraminiferal Assemblages and Meridional Hydrographic Sections in the West Pacific Ocean. Kagoshima Univ. Res. Center South Pacific, Occasional Papers, No.20, p.72 - 81, pls.l - 3.

Hatta Akio, Yasutaka Yuwaki, Kiyoshi Shimada, Sunao Masumitsu, and Masataka Higashi (1992): Me-ndional Hydrographic Sections and Planktonic Foraminiferal Assemblages in the West Pacific Ocean in 1991. Kagoshima Univ. Res. Center South Pacific, Occasional Papers, No.23, p.79 - 90, pls.l - 3. Hatta Akio, Kiyoshi Shimada, Masaki Uchiyama, Keisuke Yoshinaga, Shigeru Fujieda, Shigeki

Terada, Shiro Suwa, and Hirotaka Fujisaki (1996): Meridional Hydrographic Sections and Plank-tonic Foraminiferal Assemblages in the West Pacific Ocean in 1995. Kagoshima Univ. Res. Center South Pacific, Occasional Papers, No.30, p.69 - 83, pls.l - 3.

参照

関連したドキュメント

following [Andr´ e], Theorem 3.3.2; [NodNon], Corollary 6.4], it is of in- terest to note that this result may also be derived in the context of the theory of the present paper,

The proof uses a set up of Seiberg Witten theory that replaces generic metrics by the construction of a localised Euler class of an infinite dimensional bundle with a Fredholm

Using the batch Markovian arrival process, the formulas for the average number of losses in a finite time interval and the stationary loss ratio are shown.. In addition,

[Mag3] , Painlev´ e-type differential equations for the recurrence coefficients of semi- classical orthogonal polynomials, J. Zaslavsky , Asymptotic expansions of ratios of

We also show that the Euler class of C ∞ diffeomorphisms of the plane is an unbounded class, and that any closed surface group of genus &gt; 1 admits a C ∞ action with arbitrary

Is it possible to obtain similar results as in [COP] and in the present paper concerning John disks that are not necessarily

To an operad P one can assign a substitude by taking the canonical groupoid pinning P 1 iso Ñ P. This is not functorial in all 2-cells, only in invertible ones; it is the object part

(4S) Package ID Vendor ID and packing list number (K) Transit ID Customer's purchase order number (P) Customer Prod ID Customer Part Number. (1P)