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Int. J. Agr. Agri. R.
Akesse et al. Page 192
RESEARCH PAPER OPEN ACCESS
Study of the diet of the common cuttlefish Sepia officinalis of
the exclusive economic zone (EEZ) of Côte d'Ivoire
Ekumou V. Akesse*¹, Coffi F. Didier Adou², Mamadou Karamoko¹, Jean D. Memel¹,
Otchoumou Atcho¹
¹Formation Unit and Research of Sciences of Nature, Nangui Abrogoua University, Abidjan,
Cote d'Ivoire
²Department of Sciences and Technology, Higher Teacher Training School, Abidjan, Cote d’Ivoire
Article published on July 31, 2016
Key words: Cephalopods, Diet, Sepia officinalis, Stomachs bowl.
Abstract
The diet of the common cuttlefish Sepia officinalis was studied from samples collected in the coastal waters of
Côte d'Ivoire, for 12 months. According to the qualitative analysis of the stomach contents of all these animals,
fish and crustaceans represented respectively, 50.23% and 38.65% of the examined stomachs are the most
regularly consumed prey. The monthly evolution of the vacuity coefficient shows that this index varies according
to the sexual cycle. Juveniles feed primarily on crustaceans. The stomachs bowl of the adults contains fish but
also crustaceans and cephalopods whose frequencies are relatively significant, which would let think that Sepia
officinalis changes trophic behavior in connection with the evolution of its physiological state and that at the
adult state, the animal acquires performances which enable him to apprehend the preys with fast movements in
fact the fish.
* Corresponding Author: Ekumou V. Akesse  akessev@yahhoo.fr
International Journal of Agronomy and Agricultural Research (IJAAR)
ISSN: 2223-7054 (Print) 2225-3610 (Online)
http://www.innspub.net
Vol. 9, No. 1, p. 192-200, 2016
Int. J. Agr. Agri. R.
Akesse et al. Page 193
Introduction
The mollusc cephalopods of the exclusive economic
zone (EEZ) of the Côte d'Ivoire are the subject of
exploitation as well by the ships trawlers unloading at
the fishing port of Abidjan as by some artisanal
fishermen. Among them, is the cuttlefish Sepia
officinalis (Linnaeus, 1758), which is the species most
abundantly and regularly unloaded at the fishing port
of Abidjan and on some quays paddlers of the capital
of Ivory Coast. It is followed Octopus vulgar is
(Cuvier, 1797) and squid Loligo vulgar is (Lemark,
1798). In 2012, approximately 182.631 tons of
cuttlefish were recorded in the unloading of the
products of sea to the fishing port of Abidjan
according to the Management of the Aquiculture and
Fishing (DAP). Sepia officinal is a fishery resource
worthy of attention and able to compensate for the
over fishing of certain species of fish. It is a neritic
benthic species which prefers the sandy and muddy
bottoms. It feeds mainly on fish, crustaceans, and
other molluscs which it captures by projecting its
tentacles. Apart from some summary data available
on these marine products, some scattered in
formations learning about the biology, ecology and
cephalopod stock of the EEZ of Ivory Coast, are
available. However, the diet of the cuttlefish Sepia
officinal is captured in Ivorian waters and landed in
Abidjan has not been studied. The diet of the
cuttlefish of Senegal coasts, on the other hand, gave
places to studies by Bakhayokho (1980). The main
aim of this work is to study the trophic behavior of S.
officinal is and to describe its variability according to
the marine seasons and the classes of size of the
specimens.
Material and methods
Study area
The maritime frontage of Ivory Coast again called
exclusive economic zone (EEZ) of Ivory Coast long of
550Km of coast, constitutes a significant asset for the
development of fishing. This maritime frontage
located in the gulf of Guinea, receives various fishing
units, qualified industrial or artisanal, which help to
meet the growing needs of the population in animal
protein. The Gulf of Guinea (Fig. 1),
fishing area of Ivorian craftsmen, is located in West
Africa, in the large marine ecosystem that represent
coastal regions. It is bounded to the north by the West
African coast, south of the equator, west of the Cape
Palmas (8°W) and in the East by 2°30 E (Pezennec
and Bard, 1992). The climate is Guinean and you
meet a series of sandy beaches that form a wide arch
open to the Atlantic Ocean. Its major feature is the
presence of four marine’s seasons determined by the
temperature variation during the year (Pezennec and
Bard, 1992). So, the two cold seasons (a great, from
July to October and a small, from January to
February) are characterized by a resurgence of cold,
salty ocean water (above 35% salinity) and a low
temperature between 23 and 25°C, hot seasons are
also two (a high, from March to June and a small
November- December), and are defined by ocean
water from the sea with a lower salinity to 35 ‰ and a
high temperature of 28 and 30°C (Golé Bi et al.,
2005).
Fig. 1. Fishing zone of Ivory Coast artisanal fisheries.
Strategy of sampling and analysis of the stomachs
contents
Sampling was carried out monthly (July 2014 at June
2015) at the fishing port of Abidjan at the time of the
unloading of the trawlers and at the quay paddler of
Vridi-canal. The pelagic trawl was the machine used
for the capture of the individuals unloaded at the
fishing port and the local jig was used for those
unloaded at Vridi-canal. For the trawlers, the tide was
estimated at 8 days on average while that of the
paddlers lasted only a few hours.
Int. J. Agr. Agri. R.
Akesse et al. Page 194
Each month, a case and a basin of S. officinalis are
sampled in a random way, respectively at the fishing
port of Abidjan and the quay paddler of vridi-canal.
Taken biometric measurements are: the dorsal
mantle length (DML) in centimetre, total weight (W)
and eviscerate weight (We) in gram. After having
determined the sex and the various stages of
maturation of each individual (juveniles (<18cm) and
adult (≥18cm)), certain stomachs were analyzed on
the spot in a fresh state, and for other animals, the
part of the digestive tract lain between the
oesophagus and the stomach, was detached and
preserved in a formol solution at 5% to be examined
later on. At the laboratory the stomachs were
dissected and the contents rinsed with water on a
series of sieve of meshs 1000 μm, 500 μm and 250
μm, before being examined with the naked eye or the
binocular magnifying glass according to the size of the
individuals preys. The various preys were sorted,
counted, weighed and identified. The preys are given
as far as possible using the identification keys of
Fischer et al. (1987a; 1987b), but generally, they are
in a stage of advanced degradation and in this case,
only the solid parts, enabled us to reach the
systematic class of the prey. Principal indices already
used by several authors (Hyslop, 1980; Castro and
Guerra, 1990; Collins et al., 1994; Coelho et al., 1997)
were applied in order to determine quantitatively (Cv)
and qualitatively (F, Cn, W) the introduced preys.
Vacuity Coefficient,
VC% =
anumberofemptystomachs
anumberofexaminedstomachs
× 100
Frequency of occurrence, (F)
F% =
a number of stomach containing item i
a number of examined full stomachs
× 100
Percentage in a number of the preys, (Cn)
Cn% =
Total number of the item i
Total number of allitems
× 100
Percentage in weight of the preys,
W% =
Weightoftheitemi
Total weight of thepreys
× 100
The index of relative importance of item (IRI) (Pinkas
et al., 1971) and the food coefficient (Q) (Hureau,
1970), were used to have a more significant approach
of the diet of S. officinalis:
Index of relative importance, IRI = F%(Cn% + W%)
The expression expressed as a percentage is form:
IRI% =
IRI
∑ IRI
× 100
Food coefficient, Q = W% × Cn%
This classification takes account at the same time of
abundance and the importance in mass of the species-
preys. The classification of the species preys or groups
of species-preys is made according to values of Q. If
(Q > 200), the preys are qualified the preferential
ones; if (20 < Q < 200), the preys are secondary, and
if (Q < 20), the preys are additional.
Index of Schoener: The comparisons of the diet
between the two biological stages and the seasons
were made using the index of Schoener. It made it
possible to evaluate the degree of similarity between
the stages of maturity and the seasons.
α = 1 − 0,5(∑ ⎢pxi − pyi⎢)
𝑛
𝑘=0
Pxi = proportion of a prey i consumed by a stage of
maturity or individuals of one season (X),
Pyi = proportion of a prey i consumed by a stage of
maturity or individuals of one season (y).
The diets are considered significantly similar when
the value of α is higher than 0, 6 (α>0.6).
Statistical analysis
Using the program Statistica version 7.1, the
coefficient of correlation of the rows of Spearman was
used to see whether there is or not a relation between
the diets (probability criticizes retained: p<0. 05).
The computed values on the basis of index of relative
importance (IRI) made it possible to check the bond
between the diets of the classes of sizes and the
marine seasons.
Results
Monthly variation of the coefficient of vacuity
A total of 528 stomachs were examined during the
study period from July 2014 to June 2015 and 121
were empty. The coefficient of vacuity calculated for
this purpose is 22.91%. Its graph (Fig.2) shows the
highest percentages in the months of September and
February respectively 28.60% and 26. 02 %.
Int. J. Agr. Agri. R.
Akesse et al. Page 195
The lowest vacuity coefficients were registered the
months of April (18.06%) and May (18.1%).
Fig. 2. Monthly evolution of the coefficient of vacuity
at Sepia officinalis.
Variation of the coefficient of vacuity according to
the marine seasons
Fig. 3 gives the evolution of the coefficient of vacuity
of S. officinalis according to the marine seasons in the
exclusive economic zone of Ivory Coast. The
specimens fished during the cold seasons recorded
the highest percentages of vacuity coefficient (Great
season (26.19%) and small season (23.26%)). The
smallest percentage of vacuity was recorded during
the great hot season (19.59%).
Fig. 3.Seasonal evolution of the coefficient of vacuity
of Sepia officinalis.
GCSF (great cold season); SHS (small hot season);
SCS (small cold season); GHS (great hot season).
Variation of the coefficient of vacuity according to
the size
The graphical representation of vacuity coefficient
according to the two classes of size shows that the
coefficient of vacuity in the adults (24.21%) is higher
than that of juveniles (16.03%) (Fig. 4).
Fig. 4. Evolution of the coefficient of vacuity accor-
ding to the sizes of Sepia officinalis.
General profile of the diet
Of all the 528 stomachs of S. officinalis from the
trawler and artisanal fisheries examined, 407
contained food. Eight food categories divided into five
groups were identified (Table I). These fish, crustaceans,
cephalopods, polychaetes and plant debris. The group of
fish is constituted of fish not identified because of their
very advanced stage of digestion and two families
(Clupeidae and Polynemidae) in which are respectively,
agenus and a species. The group of crustaceans is
constituted of the shrimp Penaeus notialis and the
brachyoures (crab). A single species of cephalopod
was found in the food bowl of S. officinalis. It’s about
Sepia officinalis itself. According to classification with
the food coefficient (Table 1), fish and crustaceans are
the preferential preys with respective coefficients
Q=1069.4 and Q=680.7 (Q>200). Cephalopods
(Q=8.5), plants debris (5.08) and Polychaetes (Q=1.
65) constituted additional preys. The analysis of the
index of relative importance indicates that fish are the
preferential preys (IRI=54.37%) followed crustaceans
(IRI=43.87%). This analysis reveals that of all the
categories of consumed preys, the shrimp Penaeus
notialis is most significant (IRI=30.08%), it is
followed unspecified fish (IRI=22.62),
0
5
10
15
20
25
30
35
VC%
0
5
10
15
20
25
30
GCS SHS SCS GHS
VC%
CV%
0
5
10
15
20
25
30
youthful adults
COEFFICIENTOFVACUITY
(%)
VC%
CV%
Int. J. Agr. Agri. R.
Akesse et al. Page 196
genus Sardinella IRI=17.38), and species Galoidès
decadactylus IRI=14.37). Cephalopod (IRI=0.83),
plants debris (IRI=0.56) and polychaetes (IRI=0.37),
are regarded as accidental preys.
Variation of the diet according to the marine seasons.
The diet was analyzed according to four marine
seasons which are: the great cold season, the small
hot season, the small cold season and the great hot
season (Fig.5). In great cold season, fish (50.2%) and
crustaceans (48.76%) constituted the preferential
preys. Cephalopods (1.04) are additional preys, while
the other groups were not indexed during this season.
During the small hot season crustaceans (85.31%)
become the preferential preys and fish (14.69%)
constitute the secondary preys.
As for the other groups, they do not appear among the
preys identified during this season. In small cold
season, the diet is focused on the fish (61.01%) which
constituted the principal preys, crustaceans (38.99%)
are certainly significant in the food bowl, but
constituted secondary preys compared to fish.
During the great hot season, consumption is
dominated considerably by fish (77.81) which
constitutes the main preys. Crustaceans (15.5%) are
secondary prey, while cephalopods (6.45%),
polychaetes (0.16 %) and plant debris (0.08%) are
prey accessories (IRI<10 %). The index of Schoener
(α= 0.58) calculated on the basis of numerical
percentage (Cn), shows that the diet is significantly
different between the small hot season and the great
hot season. It shows no significant difference,
between the great hot season and the great cold
season (α=0.81), and between the great cold season
and the small cold season (α= 0.93).
This index (α=0.84) does not show variation of diet
between the small hot season and the small cold
season. The coefficient of correlation of the rows of
Spearman, calculated on the basis of indicial
percentage of food consumed during the four seasons,
indicates a significant correlation between the great
cold season and the small hot season (N=8;RS=0.
79;p<0.05),
between the great cold season and the small cold
season (N=8 RS=0.88; p<0.05) and between the
small hot season and the small cold season
(N=8RS=0.82;p<0.05). It is concluded for this
purpose a similarity between the diets those seasons
taken in pairs. This coefficient is not significant
between the great hot season and the small hot
season (N=8;RS=0.46;p<0.05) and between the great
hot season and the small cold season
(N=8;RS=0.43;p<0.05). It brings out a variation of
the diet between these last seasons.
Change in diet depending on the size of Sepia
officinalis
The collected specimens have dorsal mantle length
(DLM) ranging between 10 cm and 30 cm. Two
classes of sizes were established according to the size
of the first sexual maturity (L50).
Specimens of small size (10≤ DLM) < 18 cm)
constituted the group of juveniles and those of big
size (18≤ DLM< 30 cm), the group of adults. Fig. 6
indicates the index of relative importance of juveniles
and the adults. For the juveniles ones, the crustaceans
constituted the preys mainly consumed (%
IRI=96.56).
Among those, the shrimp Penaeus notialis, is the
principal one (% IRI = 92.99). The incidentally
consumed food, are fish (% IRI=2.71), polychaetes
(0.63) and plants debris (0.1). Cephalopod miss
stomachs contents. Regarding adults, consumption is
mostly dominated by fish (IRI=73.35%), crustaceans
(IRI=24.76%) being considered secondary prey.
Other foods represented by cephalopods (%
IRI=1.49), plant debris (% IRI=0.27) and polychaetes
(% IRI=0.13) are ingested incidentally.
The index of Schoener calculated on the basis of
numerical percentage between these two groups (α =
0.43< 0.6) shows a significant change of the diet
between juveniles ones and adults. The correlation
coefficient of Spearman calculated from the
percentages of index relative importance of juveniles
and adults was not significant (N=8; RS=0.25; p
<0.05). This reflects a change in the diet between the
two groups.
Int. J. Agr. Agri. R.
Akesse et al. Page 197
Fig. 5. Composition of the diet of Sepia officinalis
according to the marine seasons.
Note: GCS (great cold season);SHS (small hot
season);SCS (small cold season);GHS (great hot
season).
Fig. 6. Composition of the diet of Sepia officinalis
according to the sizes.
Table 1. Composition of the diet of Sepia officinalis of the EEZ of Ivory Coast and percentages of the
corresponding food indices.
Preys Cn(%) W(%) F(%) %IRI Q
fish
Unspecified fish 19,03 28,94 17,36 22,62 550,73
Sardinella sp. 15,49 14,7 18,98 17,38 227,7
Galoidès decadactylus 17,35 16,77 13,89 14,37 290,96
Crustacean
Macroures
Panaeus notialis. 22,39 21,36 22,68 30,08 478,25
Brachyoures
Crabs 13,8 14,67 15,97 13,79 202,45
Cephalopod
Sépia officinalis 4,29 1,92 4,4 0,83 8,24
Polychaetes 2,99 0,55 3,48 0,37 1,64
Plants debris 4,66 1,09 3,24 0,56 5,07
TOTAL
FISH 51,87 60,41 50,23 54,37 1069,4
CRUSTACEANS 36,19 36,03 38,65 43,87 680,7
CEPHALOPODS 4,29 1,92 4,4 0,83 8,24
POLYCHAETES 2,99 0,55 3,48 0,37 1,65
PLANTS DEBRIS 4,66 1,09 3,24 0,56 5,08
Note: Cn%: numerical percentage; W%: percentage by weight; %F: percentage of occurrence; IRI: percentage of
index of relative importance; Q:food coefficient.
Discussion
The coefficient of vacuity of the common cuttlefish
Sepia officinalis is higher during the cold seasons
than during the hot seasons, reflecting a trophic
activity significantly greater during recent seasons.
That would mean that the trophic activity of these
animals increases considerably in certain months of
the hot seasons, particularly at the time of pre-
reproduction.
The food needs to be linked to the breeding season. In
fact, for the period of breeding, the males like the
mature females, feed little. According to Richard
(1971), adults in reproduction stop feeding because
the genitals compress the digestive system, which can
partly explain the rise in the coefficient of vacuity of
these animals in the economic zone of Ivory Coast
during cold seasons.
0
20
40
60
80
100
GCS
SHC
SCS
GHS
0
20
40
60
80
100
fish
shellfish
cephalopod
polychaetes
plantsdebris
IRI%
juveniles
ADULTS
Int. J. Agr. Agri. R.
Akesse et al. Page 198
This same report was made by Hatanaka (1979),
Sanchez and Obarti (1993) on the octopus Octopus
vulgaris which is a species of Cephalopod showing
similarities with the common cuttlefish, nutritionally
and reproductively. These authors think that the
common octopus feeds more in hot season than cold
season. Vacuity coefficient is higher in mature
specimens than juveniles, this shows that, feeding
activity in juveniles is much higher compared to
adults. Our results corroborate those described by
Mangold (1982) in the Gulf of Morbihan.
He estimates that the coefficient of vacuity increases
with the age of the cuttlefish, for juveniles, high
nutrition allows rapid growth after hatching. The
classification of the items according to the two
methods (the index of relative importance: IRI and
the food coefficient: Q) makes it possible to affirm
that S. officinalis nourishes mainly fish and
crustaceans.
This is in conformity so that found others authors in
the Gulf of Tunis (Najaï et Ktari, 1979), in Ria de Vigo
(Guerra, 1985), and out of bay of Rance (Le Mao,
1985). Many fish species could not be positively
identified because of their very advanced state of
digestion; however, from fish bone, scales and other
solid parts, one could argue that it is teleost small
sizes.
The observation we made is that S. officinalis, feeds
on prey whose size is less than the predator it is.
Richard (1971) indicates also the existence of a
relationship between the size of the preys and the size
of the cuttlefish what agrees with our remarks on the
fact that the introduced preys are always lower than
the predator. The very advanced state of digestion of
stomach bowl could be explained by the fact that the
digestion of the cuttlefish is very fast. The concept of
rapid digestion was elucidated by Altman and Nixon
(1970).
According to these authors, Cephalopods secrete,
starting from posterior salivary glands a "powerful
enzyme" which acts on the attachment of the muscles
of the preys.
External digestion is followed of a very fast internal
digestion; it is practically accomplished in less than
four to six hours (Wells, quoted by Soufia NAJAI and
Mohamed Hédi KTARI, 1974). In addition to finding
pieces of flesh or arm, we identified the beaks of S.
officinalis in some examined stomachs.
This allows us to confirm the cannibal character of
cuttlefish. However he has not been given to us to find
the remains of food (remains of cephalopods) in the
stomachs of juveniles, cannibalism is related to the
size of these animals.
This phenomenon has been noted by Richard (1971),
he believes that this occurs when the animals are
under nutrition status; the weakest are always the
victims. S. officinalis diet’s does not vary
considerably according to the marine seasons, we
could say that the cuttlefish of the exclusive economic
zone of the Ivory Coast selects its prey and it is not
nourished by the availability of prey resources.
The bolus of juveniles consists mainly of crustaceans,
while the adult is mainly dominated by fish. The food
of the cuttlefish is in connection with the
physiological state of the animal. That would like to
say that in a juvenile’s state, the cuttlefish not being
able to capture faster preys, it simply feeding animals
easier to capture. Castro and Guerra (1990), noted
that during his life, the importance of crustaceans as
prey decreases the benefit of fish.
Conclusion
The food preferendum of the common cuttlefish
Sepia officinalis of the exclusive economic zone of
Ivory Coast is primarily consisted two great zoological
groups, the fish and the crustacean’s decapods.
The other categories of preys, Cephalopods
(cannibalism), polychètes and plants debris are
introduced incidentally. The diet does not vary
considerably according to the marine seasons.
However, this cephalopod food differs depending on
the size of the specimens. Indeed, as the size
increases, the individuals of this species acquire the
aptitude to catch increasingly large preys.
Int. J. Agr. Agri. R.
Akesse et al. Page 199
Acknowledgement
I wish to thank my professor, director of the pole of
research livestock productions, of university NANGUI
ABROGOUA, which directed me towards the study of
the Cephalopods. I express my gratitude in Phd of our
laboratory, which helped me to correct this
manuscript. Finally, I would like to thank all the
authors of this paper.
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de Lille, n° 2453, 264P.
Schoener TW. 1970. "Non-synchronous spatial of
lizards in patchy habitats," Ecology, vol. 51, pp. 408.

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Study of the diet of the common cuttlefish Sepia officinalis of the exclusive economic zone (EEZ) of Côte d'Ivoire

  • 1. Int. J. Agr. Agri. R. Akesse et al. Page 192 RESEARCH PAPER OPEN ACCESS Study of the diet of the common cuttlefish Sepia officinalis of the exclusive economic zone (EEZ) of Côte d'Ivoire Ekumou V. Akesse*¹, Coffi F. Didier Adou², Mamadou Karamoko¹, Jean D. Memel¹, Otchoumou Atcho¹ ¹Formation Unit and Research of Sciences of Nature, Nangui Abrogoua University, Abidjan, Cote d'Ivoire ²Department of Sciences and Technology, Higher Teacher Training School, Abidjan, Cote d’Ivoire Article published on July 31, 2016 Key words: Cephalopods, Diet, Sepia officinalis, Stomachs bowl. Abstract The diet of the common cuttlefish Sepia officinalis was studied from samples collected in the coastal waters of Côte d'Ivoire, for 12 months. According to the qualitative analysis of the stomach contents of all these animals, fish and crustaceans represented respectively, 50.23% and 38.65% of the examined stomachs are the most regularly consumed prey. The monthly evolution of the vacuity coefficient shows that this index varies according to the sexual cycle. Juveniles feed primarily on crustaceans. The stomachs bowl of the adults contains fish but also crustaceans and cephalopods whose frequencies are relatively significant, which would let think that Sepia officinalis changes trophic behavior in connection with the evolution of its physiological state and that at the adult state, the animal acquires performances which enable him to apprehend the preys with fast movements in fact the fish. * Corresponding Author: Ekumou V. Akesse  akessev@yahhoo.fr International Journal of Agronomy and Agricultural Research (IJAAR) ISSN: 2223-7054 (Print) 2225-3610 (Online) http://www.innspub.net Vol. 9, No. 1, p. 192-200, 2016
  • 2. Int. J. Agr. Agri. R. Akesse et al. Page 193 Introduction The mollusc cephalopods of the exclusive economic zone (EEZ) of the Côte d'Ivoire are the subject of exploitation as well by the ships trawlers unloading at the fishing port of Abidjan as by some artisanal fishermen. Among them, is the cuttlefish Sepia officinalis (Linnaeus, 1758), which is the species most abundantly and regularly unloaded at the fishing port of Abidjan and on some quays paddlers of the capital of Ivory Coast. It is followed Octopus vulgar is (Cuvier, 1797) and squid Loligo vulgar is (Lemark, 1798). In 2012, approximately 182.631 tons of cuttlefish were recorded in the unloading of the products of sea to the fishing port of Abidjan according to the Management of the Aquiculture and Fishing (DAP). Sepia officinal is a fishery resource worthy of attention and able to compensate for the over fishing of certain species of fish. It is a neritic benthic species which prefers the sandy and muddy bottoms. It feeds mainly on fish, crustaceans, and other molluscs which it captures by projecting its tentacles. Apart from some summary data available on these marine products, some scattered in formations learning about the biology, ecology and cephalopod stock of the EEZ of Ivory Coast, are available. However, the diet of the cuttlefish Sepia officinal is captured in Ivorian waters and landed in Abidjan has not been studied. The diet of the cuttlefish of Senegal coasts, on the other hand, gave places to studies by Bakhayokho (1980). The main aim of this work is to study the trophic behavior of S. officinal is and to describe its variability according to the marine seasons and the classes of size of the specimens. Material and methods Study area The maritime frontage of Ivory Coast again called exclusive economic zone (EEZ) of Ivory Coast long of 550Km of coast, constitutes a significant asset for the development of fishing. This maritime frontage located in the gulf of Guinea, receives various fishing units, qualified industrial or artisanal, which help to meet the growing needs of the population in animal protein. The Gulf of Guinea (Fig. 1), fishing area of Ivorian craftsmen, is located in West Africa, in the large marine ecosystem that represent coastal regions. It is bounded to the north by the West African coast, south of the equator, west of the Cape Palmas (8°W) and in the East by 2°30 E (Pezennec and Bard, 1992). The climate is Guinean and you meet a series of sandy beaches that form a wide arch open to the Atlantic Ocean. Its major feature is the presence of four marine’s seasons determined by the temperature variation during the year (Pezennec and Bard, 1992). So, the two cold seasons (a great, from July to October and a small, from January to February) are characterized by a resurgence of cold, salty ocean water (above 35% salinity) and a low temperature between 23 and 25°C, hot seasons are also two (a high, from March to June and a small November- December), and are defined by ocean water from the sea with a lower salinity to 35 ‰ and a high temperature of 28 and 30°C (Golé Bi et al., 2005). Fig. 1. Fishing zone of Ivory Coast artisanal fisheries. Strategy of sampling and analysis of the stomachs contents Sampling was carried out monthly (July 2014 at June 2015) at the fishing port of Abidjan at the time of the unloading of the trawlers and at the quay paddler of Vridi-canal. The pelagic trawl was the machine used for the capture of the individuals unloaded at the fishing port and the local jig was used for those unloaded at Vridi-canal. For the trawlers, the tide was estimated at 8 days on average while that of the paddlers lasted only a few hours.
  • 3. Int. J. Agr. Agri. R. Akesse et al. Page 194 Each month, a case and a basin of S. officinalis are sampled in a random way, respectively at the fishing port of Abidjan and the quay paddler of vridi-canal. Taken biometric measurements are: the dorsal mantle length (DML) in centimetre, total weight (W) and eviscerate weight (We) in gram. After having determined the sex and the various stages of maturation of each individual (juveniles (<18cm) and adult (≥18cm)), certain stomachs were analyzed on the spot in a fresh state, and for other animals, the part of the digestive tract lain between the oesophagus and the stomach, was detached and preserved in a formol solution at 5% to be examined later on. At the laboratory the stomachs were dissected and the contents rinsed with water on a series of sieve of meshs 1000 μm, 500 μm and 250 μm, before being examined with the naked eye or the binocular magnifying glass according to the size of the individuals preys. The various preys were sorted, counted, weighed and identified. The preys are given as far as possible using the identification keys of Fischer et al. (1987a; 1987b), but generally, they are in a stage of advanced degradation and in this case, only the solid parts, enabled us to reach the systematic class of the prey. Principal indices already used by several authors (Hyslop, 1980; Castro and Guerra, 1990; Collins et al., 1994; Coelho et al., 1997) were applied in order to determine quantitatively (Cv) and qualitatively (F, Cn, W) the introduced preys. Vacuity Coefficient, VC% = anumberofemptystomachs anumberofexaminedstomachs × 100 Frequency of occurrence, (F) F% = a number of stomach containing item i a number of examined full stomachs × 100 Percentage in a number of the preys, (Cn) Cn% = Total number of the item i Total number of allitems × 100 Percentage in weight of the preys, W% = Weightoftheitemi Total weight of thepreys × 100 The index of relative importance of item (IRI) (Pinkas et al., 1971) and the food coefficient (Q) (Hureau, 1970), were used to have a more significant approach of the diet of S. officinalis: Index of relative importance, IRI = F%(Cn% + W%) The expression expressed as a percentage is form: IRI% = IRI ∑ IRI × 100 Food coefficient, Q = W% × Cn% This classification takes account at the same time of abundance and the importance in mass of the species- preys. The classification of the species preys or groups of species-preys is made according to values of Q. If (Q > 200), the preys are qualified the preferential ones; if (20 < Q < 200), the preys are secondary, and if (Q < 20), the preys are additional. Index of Schoener: The comparisons of the diet between the two biological stages and the seasons were made using the index of Schoener. It made it possible to evaluate the degree of similarity between the stages of maturity and the seasons. α = 1 − 0,5(∑ ⎢pxi − pyi⎢) 𝑛 𝑘=0 Pxi = proportion of a prey i consumed by a stage of maturity or individuals of one season (X), Pyi = proportion of a prey i consumed by a stage of maturity or individuals of one season (y). The diets are considered significantly similar when the value of α is higher than 0, 6 (α>0.6). Statistical analysis Using the program Statistica version 7.1, the coefficient of correlation of the rows of Spearman was used to see whether there is or not a relation between the diets (probability criticizes retained: p<0. 05). The computed values on the basis of index of relative importance (IRI) made it possible to check the bond between the diets of the classes of sizes and the marine seasons. Results Monthly variation of the coefficient of vacuity A total of 528 stomachs were examined during the study period from July 2014 to June 2015 and 121 were empty. The coefficient of vacuity calculated for this purpose is 22.91%. Its graph (Fig.2) shows the highest percentages in the months of September and February respectively 28.60% and 26. 02 %.
  • 4. Int. J. Agr. Agri. R. Akesse et al. Page 195 The lowest vacuity coefficients were registered the months of April (18.06%) and May (18.1%). Fig. 2. Monthly evolution of the coefficient of vacuity at Sepia officinalis. Variation of the coefficient of vacuity according to the marine seasons Fig. 3 gives the evolution of the coefficient of vacuity of S. officinalis according to the marine seasons in the exclusive economic zone of Ivory Coast. The specimens fished during the cold seasons recorded the highest percentages of vacuity coefficient (Great season (26.19%) and small season (23.26%)). The smallest percentage of vacuity was recorded during the great hot season (19.59%). Fig. 3.Seasonal evolution of the coefficient of vacuity of Sepia officinalis. GCSF (great cold season); SHS (small hot season); SCS (small cold season); GHS (great hot season). Variation of the coefficient of vacuity according to the size The graphical representation of vacuity coefficient according to the two classes of size shows that the coefficient of vacuity in the adults (24.21%) is higher than that of juveniles (16.03%) (Fig. 4). Fig. 4. Evolution of the coefficient of vacuity accor- ding to the sizes of Sepia officinalis. General profile of the diet Of all the 528 stomachs of S. officinalis from the trawler and artisanal fisheries examined, 407 contained food. Eight food categories divided into five groups were identified (Table I). These fish, crustaceans, cephalopods, polychaetes and plant debris. The group of fish is constituted of fish not identified because of their very advanced stage of digestion and two families (Clupeidae and Polynemidae) in which are respectively, agenus and a species. The group of crustaceans is constituted of the shrimp Penaeus notialis and the brachyoures (crab). A single species of cephalopod was found in the food bowl of S. officinalis. It’s about Sepia officinalis itself. According to classification with the food coefficient (Table 1), fish and crustaceans are the preferential preys with respective coefficients Q=1069.4 and Q=680.7 (Q>200). Cephalopods (Q=8.5), plants debris (5.08) and Polychaetes (Q=1. 65) constituted additional preys. The analysis of the index of relative importance indicates that fish are the preferential preys (IRI=54.37%) followed crustaceans (IRI=43.87%). This analysis reveals that of all the categories of consumed preys, the shrimp Penaeus notialis is most significant (IRI=30.08%), it is followed unspecified fish (IRI=22.62), 0 5 10 15 20 25 30 35 VC% 0 5 10 15 20 25 30 GCS SHS SCS GHS VC% CV% 0 5 10 15 20 25 30 youthful adults COEFFICIENTOFVACUITY (%) VC% CV%
  • 5. Int. J. Agr. Agri. R. Akesse et al. Page 196 genus Sardinella IRI=17.38), and species Galoidès decadactylus IRI=14.37). Cephalopod (IRI=0.83), plants debris (IRI=0.56) and polychaetes (IRI=0.37), are regarded as accidental preys. Variation of the diet according to the marine seasons. The diet was analyzed according to four marine seasons which are: the great cold season, the small hot season, the small cold season and the great hot season (Fig.5). In great cold season, fish (50.2%) and crustaceans (48.76%) constituted the preferential preys. Cephalopods (1.04) are additional preys, while the other groups were not indexed during this season. During the small hot season crustaceans (85.31%) become the preferential preys and fish (14.69%) constitute the secondary preys. As for the other groups, they do not appear among the preys identified during this season. In small cold season, the diet is focused on the fish (61.01%) which constituted the principal preys, crustaceans (38.99%) are certainly significant in the food bowl, but constituted secondary preys compared to fish. During the great hot season, consumption is dominated considerably by fish (77.81) which constitutes the main preys. Crustaceans (15.5%) are secondary prey, while cephalopods (6.45%), polychaetes (0.16 %) and plant debris (0.08%) are prey accessories (IRI<10 %). The index of Schoener (α= 0.58) calculated on the basis of numerical percentage (Cn), shows that the diet is significantly different between the small hot season and the great hot season. It shows no significant difference, between the great hot season and the great cold season (α=0.81), and between the great cold season and the small cold season (α= 0.93). This index (α=0.84) does not show variation of diet between the small hot season and the small cold season. The coefficient of correlation of the rows of Spearman, calculated on the basis of indicial percentage of food consumed during the four seasons, indicates a significant correlation between the great cold season and the small hot season (N=8;RS=0. 79;p<0.05), between the great cold season and the small cold season (N=8 RS=0.88; p<0.05) and between the small hot season and the small cold season (N=8RS=0.82;p<0.05). It is concluded for this purpose a similarity between the diets those seasons taken in pairs. This coefficient is not significant between the great hot season and the small hot season (N=8;RS=0.46;p<0.05) and between the great hot season and the small cold season (N=8;RS=0.43;p<0.05). It brings out a variation of the diet between these last seasons. Change in diet depending on the size of Sepia officinalis The collected specimens have dorsal mantle length (DLM) ranging between 10 cm and 30 cm. Two classes of sizes were established according to the size of the first sexual maturity (L50). Specimens of small size (10≤ DLM) < 18 cm) constituted the group of juveniles and those of big size (18≤ DLM< 30 cm), the group of adults. Fig. 6 indicates the index of relative importance of juveniles and the adults. For the juveniles ones, the crustaceans constituted the preys mainly consumed (% IRI=96.56). Among those, the shrimp Penaeus notialis, is the principal one (% IRI = 92.99). The incidentally consumed food, are fish (% IRI=2.71), polychaetes (0.63) and plants debris (0.1). Cephalopod miss stomachs contents. Regarding adults, consumption is mostly dominated by fish (IRI=73.35%), crustaceans (IRI=24.76%) being considered secondary prey. Other foods represented by cephalopods (% IRI=1.49), plant debris (% IRI=0.27) and polychaetes (% IRI=0.13) are ingested incidentally. The index of Schoener calculated on the basis of numerical percentage between these two groups (α = 0.43< 0.6) shows a significant change of the diet between juveniles ones and adults. The correlation coefficient of Spearman calculated from the percentages of index relative importance of juveniles and adults was not significant (N=8; RS=0.25; p <0.05). This reflects a change in the diet between the two groups.
  • 6. Int. J. Agr. Agri. R. Akesse et al. Page 197 Fig. 5. Composition of the diet of Sepia officinalis according to the marine seasons. Note: GCS (great cold season);SHS (small hot season);SCS (small cold season);GHS (great hot season). Fig. 6. Composition of the diet of Sepia officinalis according to the sizes. Table 1. Composition of the diet of Sepia officinalis of the EEZ of Ivory Coast and percentages of the corresponding food indices. Preys Cn(%) W(%) F(%) %IRI Q fish Unspecified fish 19,03 28,94 17,36 22,62 550,73 Sardinella sp. 15,49 14,7 18,98 17,38 227,7 Galoidès decadactylus 17,35 16,77 13,89 14,37 290,96 Crustacean Macroures Panaeus notialis. 22,39 21,36 22,68 30,08 478,25 Brachyoures Crabs 13,8 14,67 15,97 13,79 202,45 Cephalopod Sépia officinalis 4,29 1,92 4,4 0,83 8,24 Polychaetes 2,99 0,55 3,48 0,37 1,64 Plants debris 4,66 1,09 3,24 0,56 5,07 TOTAL FISH 51,87 60,41 50,23 54,37 1069,4 CRUSTACEANS 36,19 36,03 38,65 43,87 680,7 CEPHALOPODS 4,29 1,92 4,4 0,83 8,24 POLYCHAETES 2,99 0,55 3,48 0,37 1,65 PLANTS DEBRIS 4,66 1,09 3,24 0,56 5,08 Note: Cn%: numerical percentage; W%: percentage by weight; %F: percentage of occurrence; IRI: percentage of index of relative importance; Q:food coefficient. Discussion The coefficient of vacuity of the common cuttlefish Sepia officinalis is higher during the cold seasons than during the hot seasons, reflecting a trophic activity significantly greater during recent seasons. That would mean that the trophic activity of these animals increases considerably in certain months of the hot seasons, particularly at the time of pre- reproduction. The food needs to be linked to the breeding season. In fact, for the period of breeding, the males like the mature females, feed little. According to Richard (1971), adults in reproduction stop feeding because the genitals compress the digestive system, which can partly explain the rise in the coefficient of vacuity of these animals in the economic zone of Ivory Coast during cold seasons. 0 20 40 60 80 100 GCS SHC SCS GHS 0 20 40 60 80 100 fish shellfish cephalopod polychaetes plantsdebris IRI% juveniles ADULTS
  • 7. Int. J. Agr. Agri. R. Akesse et al. Page 198 This same report was made by Hatanaka (1979), Sanchez and Obarti (1993) on the octopus Octopus vulgaris which is a species of Cephalopod showing similarities with the common cuttlefish, nutritionally and reproductively. These authors think that the common octopus feeds more in hot season than cold season. Vacuity coefficient is higher in mature specimens than juveniles, this shows that, feeding activity in juveniles is much higher compared to adults. Our results corroborate those described by Mangold (1982) in the Gulf of Morbihan. He estimates that the coefficient of vacuity increases with the age of the cuttlefish, for juveniles, high nutrition allows rapid growth after hatching. The classification of the items according to the two methods (the index of relative importance: IRI and the food coefficient: Q) makes it possible to affirm that S. officinalis nourishes mainly fish and crustaceans. This is in conformity so that found others authors in the Gulf of Tunis (Najaï et Ktari, 1979), in Ria de Vigo (Guerra, 1985), and out of bay of Rance (Le Mao, 1985). Many fish species could not be positively identified because of their very advanced state of digestion; however, from fish bone, scales and other solid parts, one could argue that it is teleost small sizes. The observation we made is that S. officinalis, feeds on prey whose size is less than the predator it is. Richard (1971) indicates also the existence of a relationship between the size of the preys and the size of the cuttlefish what agrees with our remarks on the fact that the introduced preys are always lower than the predator. The very advanced state of digestion of stomach bowl could be explained by the fact that the digestion of the cuttlefish is very fast. The concept of rapid digestion was elucidated by Altman and Nixon (1970). According to these authors, Cephalopods secrete, starting from posterior salivary glands a "powerful enzyme" which acts on the attachment of the muscles of the preys. External digestion is followed of a very fast internal digestion; it is practically accomplished in less than four to six hours (Wells, quoted by Soufia NAJAI and Mohamed Hédi KTARI, 1974). In addition to finding pieces of flesh or arm, we identified the beaks of S. officinalis in some examined stomachs. This allows us to confirm the cannibal character of cuttlefish. However he has not been given to us to find the remains of food (remains of cephalopods) in the stomachs of juveniles, cannibalism is related to the size of these animals. This phenomenon has been noted by Richard (1971), he believes that this occurs when the animals are under nutrition status; the weakest are always the victims. S. officinalis diet’s does not vary considerably according to the marine seasons, we could say that the cuttlefish of the exclusive economic zone of the Ivory Coast selects its prey and it is not nourished by the availability of prey resources. The bolus of juveniles consists mainly of crustaceans, while the adult is mainly dominated by fish. The food of the cuttlefish is in connection with the physiological state of the animal. That would like to say that in a juvenile’s state, the cuttlefish not being able to capture faster preys, it simply feeding animals easier to capture. Castro and Guerra (1990), noted that during his life, the importance of crustaceans as prey decreases the benefit of fish. Conclusion The food preferendum of the common cuttlefish Sepia officinalis of the exclusive economic zone of Ivory Coast is primarily consisted two great zoological groups, the fish and the crustacean’s decapods. The other categories of preys, Cephalopods (cannibalism), polychètes and plants debris are introduced incidentally. The diet does not vary considerably according to the marine seasons. However, this cephalopod food differs depending on the size of the specimens. Indeed, as the size increases, the individuals of this species acquire the aptitude to catch increasingly large preys.
  • 8. Int. J. Agr. Agri. R. Akesse et al. Page 199 Acknowledgement I wish to thank my professor, director of the pole of research livestock productions, of university NANGUI ABROGOUA, which directed me towards the study of the Cephalopods. I express my gratitude in Phd of our laboratory, which helped me to correct this manuscript. Finally, I would like to thank all the authors of this paper. References Altman S, Nixon M. 1970. Use of the beaks and radula by Octopus vulgaris in feeding. Journal Zoologique London 161, 25-38. Bakhayokho M. 1980. Pêche et biologie des céphalopodes exploités sur les côtes du Sénégal (12°20N- 16°03N). Thèse de spécialité (3ème cycle), Mention biologie, UniversitédeBretagne Occidentale, Brest 119 p. Castro B, Guerra A. 1990. The diet of Sepia officinalis (Linnaeus, 1758) and Sepia elegans (D’Orbigny, 1835) (Cephalopoda, Sepioidea) from the Ria de Vigo (NW Spain). Scientia Marina 54, 375-388. Coelho M, Domingues P, Balguerias E, Fernandez M, Andrade JP. 1997. A comparative study of diet of Loligo vulgaris (Lamarck, 1799) (Mollusca: Cephalopoda) from the south coast of Portugal and the Saharan Bank (Central-East Atlantic). Fisheries Research, 29, 245–255. Collins MA, De Grave S, Lordan C, Burnell GM, Rodhouse PG. 1994. Diet of the squid Loligo forbesi Steen strup (Cephalopoda: Loliginidae) in Irish waters. ICES Journal of Marine Science 51, 337-344. Direction de l’aquaculture et des pêches DAP. 2012. Annuaire des statistiques des pêches et de l’aquaculture 25p. Fischer W, Bauchot ML, Schneider M. 1987a. Méditerranée et Mer Noire. Invertébrés. Fiches d’identification des espèces pour les besoins de la pêche. Rome I , 1-760. Fischer W, Bauchot ML, Schneider M. 1987b. Méditerranée et Mer Noire. Vertébrés. Fiches d’identification des espèces pour les besoins de la pêche. Rome II, 761-1530. Gole Bi GG, Koffi KJD, Dadi SG. 2005. Contribution socio-économique de la pêche artisanale en Côte d'Ivoire. DFID, Programme pour des Moyens d’Existence Durables dans la Pêche (PMEDP) en Afrique de l’Ouest (GCP/INT/735/UK). GUERRA A, 1985. Food of the cuttlefish Sepia officinalis and Sepia esculentain the Ria de Vigo (N.W. Spain) (Mollusca: Cephalopoda). Jlool. Ser A.GBR 207(4), 511-519. Hatanaka H. 1979. Studies on the fisheries biology of common Octopus off the north-west coast of Africa. Bull Far Seas Fish Res Lab 17, 13-124. Hureau JC, 1970. Biologie comparée de quelques poissons antarctiques (Nototheniidae). Bull. Inst. Océanogr. Monaco 68(1391), 1-245. Hyslop EJ. 1980. Stomach contents analysis. A review of methods and their application. Journal Fish Biological 17, 411-429. LE MAO P. 1985. Place de la seiche Sepia officinalis (Mollusque Céphalopode) dans les chaînes alimentaires du Golfe Normado-Breton. Cahier Biologie Marine XXVI 331-340. Mangold K. 1982. Quelques aspects de la croissance des céphalopodes. Océanis 8, 533-549. NAJAI S, KTARI M. 1974. Etude du régime alimentaire de la seiche commune Sepia of ficinalis Linné, 1758 (Mollusque, Céphalopode) du golfe de Tunis. Bulletin Institut National Scientifique Technique Océanographique. Pêche Salammbo 6(1-4), 53-61. Pezennec O, Bard FX. 1992. Importance écolo- gique de la petite saison d’upwelling ivoiro-ghané- enne etchangements dans la pêcherie de Sardinella aurita. Aquaculture Living resource 5, 249-259. Pinkas L, Oliphant MS, Iverson LK. 1971. Food habits of albacore, blue fin tuna and bonito in Californian waters. Calif. Fish. Game 152, 1-105.
  • 9. Int. J. Agr. Agri. R. Akesse et al. Page 200 RICHARD A. 1971. Contribution à l'étude expérimentale de la croissance et de la maturation sexuelle de la seiche Sepia officinalis L. (Mollusque: Céphalopode). Thèse de Doctorat d'Etat, Université de Lille, n° 2453, 264P. Schoener TW. 1970. "Non-synchronous spatial of lizards in patchy habitats," Ecology, vol. 51, pp. 408.