DONNEES BIBLIOGRAPHIQUES CONCERNANT LA RELATION
TAILLE-POIDS, LA CROISSANCE ET LA REPRODUCTION
DES PRINCIPALES ESPECES PELAGIQUES
Source: GT CRODT/CNROP
Novadhibou, juin 1988
DECAPTERUS RHONCHUS | Relation taille-poids | P=aL'b | |
ANNEE | PARAMETRE | PARAMETRE | UNITE | UNITE | GAMME DE | ZONES | SOURCES | NATIONALITE |
| a | b | P | L | TAILLE | | | |
1972–1974 | 0.0799232 | 2.50429 | GR | LFCM | 22–40 | 17–26°N | MAXIMET STALCU, 1976 | ROUMANIE |
1975–1976 | 0.01243 | 3.055 | GR | LFCM | 4–41 | SENEGAL | FAO, 1984(p11) | SENEGAL |
? | 0.006521 | 3.097 | GR | LTCM | ? | ? | FAO, 1984 (p12) | POLOGNE |
1981 | 0.0125 | 2.9092 | GR | LTCM | 26–45 | MAURITANIE | FAO, 1984 (p10) | RDA |
? | 0.02 | 2.88 | GR | LFCM | 15–40 | SAHARA-M. | FAO, 1984 (p11) | URSS |
1982(1°trim) | 0.0204 | 2.7991 | GR | LTCM | 21–30 | MAURITANIE | HOLZLOHNER & AL, 1983 | RDA |
1982(2°trim) | 0.0083 | 3.0286 | GR | LTCM | 13–33 | MAURITANIE | HOLZLOHNER & AL, 1983 | RDA |
1982(3°trim) | 0.0145 | 2.8545 | GR | LTCM | 17–33 | MAURITANIE | HOLZLOHNER & AL, 1983 | RDA |
1982(4°trim) | 0.0237 | 2.7351 | GR | LTCM | 15–33 | MAURITANIE | HOLZLOHNER & AL, 1983 | RDA |
1980 | 0.0149 | 2.8838 | GR | LTCM | 26–44 | MAURITANIE | HOFFMANN, 1987 | RDA |
1981 | 0.0129 | 2.9145 | GR | LTCM | 26–49 | MAURITANIE | HOFFMANN, 1987 | RDA |
1982 | 0.0209 | 2.7769 | GR | LTCM | 22–45 | MAURITANIE | HOFFMANN, 1987 | RDA |
1983 | 0.008 | 3.1656 | GR | LFCM | 17–39 | MAURITANIE | HOFFMANN, 1987 | RDA |
1984 | 0.0336 | 2.7467 | GR | LFCM | 23–37 | MAURITANIE | HOFFMANN, 1987 | RDA |
1985 | 0.142 | 2.9647 | GR | LFCM | 7–38 | MAURITANIE | MIMEO, 1987 | RDA |
1986 | 0.01233 | 3.0608 | GR | LFCM | 7–38 | SENEGAL | CAMARENA, 1986 | SENEGAL |
1987–88 | 0.021 | 2.91 | GR | LFCM | 19–38 | MAURITANIE | LAWAL & MYLNIKOV, 1988 | MAURITANIE |
1988 | 0.035 | 2.7313 | GR | LFCM | 20–40 | 34.1.3–34.3.1 | CONSTANTIN MAXIM | ROUMANIE |
# présenté au groupe de travail mais non puclié
SCOMBER JAPONICUS | | Relation taille-poids | P=aL'b | |
ANNEE | PARAMETRE | PARAMETRE | UNITE | UNITE | GAMME DE | ZONES | SOURCES | NATIONALITE |
| a | b | P | L | TAILLE | | | |
1970–73 | 0.001935512 | 3.5675675 | GR | LFCM | 14–43 | 12–29°N | FAO, 1984 (p14) | ROUMANIE |
1975–82? | 0.00407 | 3.3 | GR | LFCM | 9–39 | MAROC | FAO, 1984 (p110) | MAROC |
1978? | 0.004871 | 3.278 | GR | LFCM | 8–41 | SENEGAL | FAO, 1979(p124) | SENEGAL |
1981 | 0.0018 | 3.4744 | GR | LFCM | 26–48 | MAURITANIE | HOLZLOHNER & K., 1982 | RDA |
1982(2°trim) | 0.0022 | 3.437 | GR | LFCM | 32–42 | MAURITANIE | HOLZLOHNER & AL, 1983 | RDA |
1982(3°trim) | 0.0006 | 3.8071 | GR | LFCM | 26–36 | MAURITANIE | HOLZLOHNER & AL, 1983 | RDA |
1982(4°trim) | 0.0014 | 3.5573 | GR | LFCM | 25–48 | MAURITANIE | HOLZLOHNER & AL, 1983 | RDA |
? | 0.003916 | 3.352 | GR | LFCM | ?–53 | SAH-MAU-SEN | FAO, 1984,(p14) | URSS |
1984–85 | 0.003892 | 3.3619 | GR | LFCM | 6–41 | SENEGAL | CAMARENA, 1986 | SENEGAL |
1987–88 | 0.000189 | 3.577 | GR | LFCM | 11–44 | MAURITANIE | LAWAL & MYLNIKOV, 1988 | MAURITANIE |
1988 | 0.00206 | 3.5505 | GR | LFCM | 16–43 | 34.1.3–34.3.1 | CONSTANTIN MAXIM | ROUMANIE |
SARDINELLA AURITA | | Relation taille-poids | P=aL'b | |
ANNEE | PARAMETRE | PARAMETRE | UNITE | UNITE | GAMME DE | ZONES | SOURCES | NATIONALITE |
| a | b | P | L | TAILLE | | | |
1968–69males | 0.00000185 | 3.388 | GR | LFmm | | SENEGAL | BOELY, 1979 | SENEGAL |
femelles | 0.00000197 | 3.3768 | GR | LFmm | | SENEGAL | BOELY, 1979 | SENEGAL |
indet | 0.00000326 | 3.2817 | GR | LFmm | | SENEGAL | BOELY, 1979 | SENEGAL |
tot | 0.00000525 | 3.1943 | GR | LFmm | | SENEGAL | BOELY, 1979 | SENEGAL |
1968(1° trim) | 0.00000345 | 3.2816 | GR | LFmm | | SENEGAL | BOELY, 1979 | SENEGAL |
1968(2° trim) | 0.000002353 | 3.3363 | GR | LFmm | | SENEGAL | BOELY, 1979 | SENEGAL |
1968(3° trim) | 0.000005224 | 3.1953 | GR | LFmm | | SENEGAL | BOELY, 1979 | SENEGAL |
1968(4° trim) | 0.000000012 | 3.0342 | GR | LFmm | | SENEGAL | BOELY, 1979 | SENEGAL |
1969(1° trim) | 0.000002229 | 3.3506 | GR | LFmm | | SENEGAL | BOELY, 1979 | SENEGAL |
1969(2° trim) | 0.000003815 | 3.2583 | GR | LFmm | | SENEGAL | BOELY, 1979 | SENEGAL |
1969(3° trim) | 0.00000039 | 2.813 | GR | LFmm | | SENEGAL | BOELY, 1979 | SENEGAL |
1969(4° trim) | 0.00007417 | 3.1123 | GR | LFmm | | SENEGAL | BOELY, 1979 | SENEGAL |
1976–77? | 0.006392 | 3.274 | GR | LFcm | 4–32 | SENEGAL | FAO, 1979(p122) | SENEGAL |
? | 0.01648 | 2.8386 | GR | LTCM | | AFRIQUE O. | FAO, 1979(p7) | |
1981 | 0.0024471 | 3.3751 | GR | LTCM | 22–37 | MAURITANIE | HOLZLOHNER & K., 1982 | RDA |
1982(1° trim) | 0.004 | 3.8854 | GR | LTCM | 31–40 | MAURITANIE | HOLZLOHNER & AL, 1983 | RDA |
1982(2°trim) | 0.0038 | 3.2607 | GR | LTCM | 27–38 | MAURITANIE | HOLZLOHNER & AL, 1983 | RDA |
1982(3°trim) | 0.01 | 2.9725 | GR | LTCM | 26–40 | MAURITANIE | HOLZLOHNER & AL, 1983 | RDA |
1982(4°trim) | 0.003 | 3.3398 | GR | LTCM | 16-36 | MAURITANIE | HOLZLOHNER & AL, 1983 | RDA |
1984–85 | 0.0061104 | 3.2901 | GR | LFCM | 5–32 | SENEGAL | CAMARENA, 1986 | SENEGAL |
1987–88 | 0.00794 | 3.2278 | GR | LFCM | 15–32 | MAURITANIE | LAWAL & MYLNIKOV, 1988 | MAURITANIE |
1988 | 0.0129 | 3.0596 | GR | LFCM | 15–35 | 34.1.3–34.3.1 | CONSTANTIN MAXIM | ROUMANIE |
SARDINELLA MADERENSIS | Relation taille-poids | P=aL'b | |
ANNEE | PARAMETRE | PARAMETRE | UNITE | UNITE | GAMME DE | ZONES | SOURCES | NATIONALITE |
| a | b | P | L | TAILLE | | | |
1975–77? | 0.01034 | 3.142 | GR | LFCM | 4–29 | SENEGAL | FAO, 1979 (p123) | SENEGAL |
1982(1° trim) | 0.018 | 2.8328 | GR | LTCM | 32–38 | MAURITANIE | HOLZLOHNER & AL, 1983 | RDA |
1982(3° trim) | 0.0264 | 2.7202 | GR | LTCM | 28–38 | MAURITANIE | HOLZLOHNER & AL, 1983 | RDA |
1982(4° trim) | 0.0053 | 3.163 | GR | LTCM | 25–37 | MAURITANIE | HOLZLOHNER & AL, 1983 | RDA |
1984–85 | 0.0098535 | 3.1673 | GR | LFCM | 5–29 | SENEGAL | CAMARENA, 1986 | SENEGAL |
1985 | 0.0229297 | 2.778069 | GR | LFCM | 7–29 | CAP-VERT | FAO, 1987 (p150) | CAP-VERT |
1987–88 | 0.0098 | 3.183 | GR | LFCM | 8–3 | MAURITANIE | LAWAL & MYLNIKOV, 1988 | MAURITANIE |
1988 | 0.0092 | 3.1695 | GR | LFCM | 16–31 | 34.1.3–34.3.1 | CONSTANTIN MAXIM | ROUMANIE |
TRACHURUS TRACHURUS | Relation-taille-poids | P=aL'b | |
ANNEE | PARAMETRE | PARAMETRE | UNITE | UNITE | GAMME DE | ZONES | SOURCES | NATIONALITE |
| a | b | P | L | TAILLE | | | |
1978–79 | 0.019 | 2.876 | GR | ?CM | >16CM | MAROC | FAO, 1984 (p130) | MAROC |
? | 0.023 | 2.505 | GR | ?CM | <10 CM | MAROC | FAO, 1984 (p130) | MAROC |
? | 0.005 | 3.12 | GR | ?CM | >10 CM | MAROC | FAO, 1984 (p130) | MAROC |
1973 | 0.0197 | 2.85 | GR | LFCM | 18–34 | 20–26°N | FAO, 1984 (p53) | ROUMANIE |
1974 | 0.0106 | 3.05 | GR | LFCM | 6–34 | 20–26°N | FAO, 1984 (p53) | ROUMANIE |
1975 | 0.0207 | 2.85 | GR | LFCM | 9–32 | 20–26°N | FAO, 1984 (p53) | ROUMANIE |
1976 | 0.0089 | 3.09 | GR | LFCM | 9–35 | 20–25°N | FAO, 1984 (p53) | ROUMANIE |
1977 | 0.0292 | 2.73 | GR | LFCM | 10–32 | 17–29°N | FAO, 1984 (p53) | ROUMANIE |
1978 | 0.0208 | 2.83 | GR | LFCM | 17–35 | 16–24°N | FAO, 1984 (p53) | ROUMANIE |
1979 | 0.0446 | 2.6 | GR | LFCM | 14–36 | 16–23°N | FAO, 1984 (p53) | ROUMANIE |
1980 | 0.0125 | 2.98 | GR | LFCM | 12–34 | MAURITANIE | FAO, 1984 (p53) | ROUMANIE |
1981 | 0.0198 | 2.85 | GR | LFCM | 17–33 | MAURITANIE | FAO, 1984 (p53) | ROUMANIE |
1982 | 0.0128 | 2.99 | GR | LFCM | 10–37 | MAURITANIE | FAO, 1984 (p53) | ROUMANIE |
1981 | 0.0265 | 2.685 | GR | LFCM | 25–43 | MAURITANIE | FAO, 1984 (p3) | RDA |
1982(1° trim) | 0.0087 | 2.2995 | GR | LFCM | 27–40 | MAURITANIE | HOLZLOWNER & AL, 1983 | RDA |
1982(2° trim) | 0.0388 | 2.5943 | GR | LFCM | 31–40 | MAURITANIE | HOLZLOWNER & AL, 1983 | RDA |
1982(3° trim) | 0.0023 | 3.3803 | GR | LFCM | 21–37 | MAURITANIE | HOLZLOWNER & AL, 1983 | RDA |
1982(4° trim) | 0.0096 | 3.1484 | GR | LFCM | 25–41 | MAURITANIE | HOLZLOWNER & AL, 1983 | RDA |
? | 0.01 | 3.02 | GR | LFCM | 14–36 | 14–36°N | FAO, 1984 (p3) | URSS |
? | 0.0049 | 3.14 | GR | LFCM | ? | ? | FAO, 1979 (p9) | POLOGNE |
1981 | 0.027 | 2.6936 | GR | LFCM | 20–45 | MAURITANIE | HOFFMANN, 1987 | RDA |
1982 | 0.0545 | 2.4785 | GR | LFCM | 7–40 | MAURITANIE | HOFFMANN, 1987 | RDA |
1983 | 0.0128 | 2.9986 | GR | LFCM | 17–35 | MAURITANIE | HOFFMANN, 1987 | RDA |
1984 | 0.015 | 2.9364 | GR | LFCM | 14–38 | MAURITANIE | HOFFMANN, 1987 | RDA |
1987–88 | 0.008 | 3.147 | GR | LFCM | 8–34 | MAURITANIE | LAWAL ET MYLNIKOV, 1988 | MAURITANIE |
1988 | 0.0139 | 2.9606 | GR | LFCM | 14–37 | 34.1.3–34.3.1 | CONSTANTIN MAXIM, 1988 | MAURITANIE |
TRACHURUS TRECAE | Relation-taille-poids | P=aL'b | |
ANNEE | PARAMETRE | PARAMETRE | UNITE | UNITE | GAMME DE | ZONES | SOURCES | NATIONALITE |
| a | b | P | L | TAILLE | | | |
1976? | 0.1489 | 2.954 | GR | LFCM | 7–40 | SENEGAL | FAO, 1979 (p126) | SENEGAL |
1977? | 0.01 | 2.98 | GR | LFCM | 8–43 | | FAO, 1984 (p7) | URSS |
1973 | 0.0247 | 2.8 | GR | LFCM | 16–32 | 20–26°N | FAO, 1984 (p53) | ROUMANIE |
1974 | 0.0314 | 2.72 | GR | LFCM | 12–33 | 20–26°N | FAO, 1984 (p53) | ROUMANIE |
1975 | 0.0145 | 2.96 | GR | LFCM | 18–31 | 20–26°N | FAO, 1984 (p53) | ROUMANIE |
1976 | 0.0101 | 3.07 | GR | LFCM | 15–30 | 20–25°N | FAO, 1984 (p53) | ROUMANIE |
1981 | 0.0083 | 3.11 | GR | LFCM | 9–30 | MAURITANIE | FAO, 1984 (p53) | ROUMANIE |
1982 | 0.0248 | 2.8 | GR | LFCM | 14–35 | MAURITANIE | FAO, 1984 (p53) | ROUMANIE |
1982 | 0.0248344 | 2.8090175 | GR | LFCM | 14–36 | MAURITANIE | FAO, 1984 (p7) | RDA |
1981 | 0.0106 | 2.9368 | GR | LFCM | 14–44 | MAURITANIE | FAO, 1984 (p7) | RDA |
1982(1° trim) | 0.0062 | 3.0612 | GR | LFCM | 19–37 | MAURITANIE | HOLZLOHNER & AL, 1983 | RDA |
1982(2° trim) | 0.025 | 2.717 | GR | LFCM | 24–44 | MAURITANIE | HOLZLOHNER & AL, 1983 | RDA |
1982(3° trim) | 0.0057 | 3.1232 | GR | LFCM | 21–45 | MAURITANIE | HOLZLOHNER & AL, 1983 | RDA |
1982(4° trim) | 0.0138 | 2.8722 | GR | LFCM | 19–49 | MAURITANIE | HOLZLOHNER & AL, 1983 | RDA |
1984–85 | 0.01569 | 3.0422 | GR | LFCM | 9–34 | SENEGAL | CAMARENA, 1986 | SENEGAL |
1987–88 | 0.011 | 3.041 | GR | LFCM | 4–41 | MAURITANIE | LAWAL & MYLNIKOV, 1988 | MAURITANIE |
1988 | 0.0186 | 2.8853 | GR | LFCM | 11–39 | 34.13–34.3.1 | CONSTANTIN MAXIM | ROUMANIE |
DECAPTERUS RHONCHUS | Paramètres de croissance | | |
ANNEE | LINFINI | K | tO | GAMME DE TAILLE(cm) | ZONES | METHODES | SOURCES | NATIONALITE |
? | 48.57 | 0.16 | -0.8 | LT | 14–21°N | OTOLITHES | FAO, 1979 (p 12) | URSS |
? | 45.3 | 0.303 | -0.515 | LT | ? | OTOLITHES | FAO, 1979 (p 12) | POLOGNE |
1972–74 | 55.69 | 0.136 | -1.295 | LF | SEN.-MAURIT. | ECAILLES | MAXIM 1 STAIC, 1976 | ROUMANIE |
? | 44 | 0.448 | 0.114 | LF | SENEGAL | ? | FAO, 1984 (p 12) | SENEGAL |
1980 | 52.73 | 0.2713 | -0.182 | LT | MAURITANIE | OTOLITHES | HOFFMANN, 1987 | RDA |
1981 | 58.72 | 0.1474 | -2.336 | LT | MAURITANIE | OTOLITHES | HOFFMANN, 1987 | RDA |
1982 | 55.14 | 0.1986 | -1.18 | LT | MAURITANIE | OTOLITHES | HOFFMANN, 1987 | RDA |
1983 | 47.8 | 0.1614 | -2.212 | LF | MAURITANIE | OTOLITHES | HOFFMANN, 1987 | RDA |
1984 | 42.13 | 0.2426 | -1.567 | LF | MAURITANIE | OTOLITHES | HOFFMANN, 1987 | RDA |
1985 | 51.55 | 0.1524 | -1.839 | LF | MAURITANIE | OTOLITHES | ## | RDA |
1982(2° trim) | 43.585 | 0.3461 | -0.959 | LT | MAURITANIE | OTOLITHES | HOLZLOHNER & AL, 1983 | RDA |
1982(3° trim) | 48.271 | 0.2661 | -1.258 | LT | MAURITANIE | OTOLITHES | HOLZLOHNER & AL, 1983 | RDA |
1982(4° trim) | 50.609 | 0.2133 | -1.592 | LT | MAURITANIE | OTOLITHES | HOLZLOHNER & AL, 1983 | RDA |
# préconisé par le groupe de travail
SCOMBER JAPONICUS | Paramètres de croissance | | |
ANNEE | LINFINI | K | tO | GAMME DE TAILLE(cm) | ZONES | METHODES | SOURCES | NATIONALITE |
1972–73 | 55.357 | 0.118 | -3.178 | 29-LF-44 | 17–26°N | ECAILLES | STAICU & MAXIM, 1974 | ROUMANIE |
? | 44.08 | 0.326 | -0.834 | 20-LF-39 | SAHARA | ECAILLES | FAO, 1979 (p 130) | URSS |
? | 48.743 | 0.201 | -2.963 | 19-LT-43 | SEN-MAURIT | OTOLITHES | FAO, 1984 (p 14) | RDA |
? | 44.096 | 0.309 | -1.011 | LF | 34.1.3 | OTOLITHES | FAO, 1984 (p 15) | URSS |
1982 (2° trim) | 44.825 | 0.339 | -1.037 | 32-LT-42 | MAURITANIE | OTOLITHES | HOLZLOHNER & AL, 1983 | RDA |
1982 (4° trim) | 67.515 | 0.1086 | -2.515 | 25-LT-48 | MAURITANIE | OTOLITHES | HOLZLOHNER & AL, 1983 | RDA |
1984–85 | 51.69 | 0.217 | -0.891 | 18-LF-41 | SENEGAL | ECAILLES | CAMARENA, 1986 | SENEGAL |
# préconisé par le groupe de travail
SARDINELLA AURITA | Paramètres de croissance | | |
ANNEE | LINFINI | K | tO | GAMME DE TAILLE(cm) | ZONES | METHODES | SOURCES | NATIONALITE |
1966–77 | 30.63 | 1.206 | -0.062 | 6-LF-32 | SENEGAL | FREQ.TAILLE & ECAILLES | BOELY & AL, 1982 | SENEGAL |
1984–85 | 31.93 | 0.613 | -0.745 | 17-LF-32 | SENEGAL | ECAILLES | CAMARENA, 1986 | SENEGAL |
? | 40.7 | 0.326 | -0.6283 | LT | MAURITANIE | ? | PHAM THUOC et SZYPULA, 1973 | ? |
S. MADERENSIS | Paramètres de croissance | | |
ANNEE | LINFINI | K | tO | GAMME DE TAILLE(cm) | ZONES | METHODES | SOURCES | NATIONALITE |
1980–82 | 39.5 | 0.45 | | 9-LF-30 | SENEGAL | FREQ. TAILLE | SAMB, 1986 | SENEGAL |
1980–82 | 37.5 | 0.3 | | 9-LF-30 | SENEGAL | FREQ. TAILLE | SAMB, 1986 | SENEGAL |
| (wp=0.1 | c=0.6)# | | | | | | |
1984-85 | 30.34 | 0.49 | -0.589 | 8-LF-30 | SENEGAL | FREQ. TAILLE ET ECAILLES | CAMARENA, 1986 | SENEGAL |
T. TRACHURUS | Paramètres de croissance | | |
ANNEE | LINFINI | K | tO | GAMME DE TAILLE(cm) | ZONES | METHODES | SOURCES | NATIONALITE |
? | 37.98 | 0.25 | -0.98 | LF | 21.26°N | ECAILLES | FAO, 1984 (p 9) | URSS |
? | 50 | 0.13 | -2.32 | LT | ? | OTOLITHES | FAO, 1984 (p 9) | POLOGNE |
? | 43.55 | 0.19 | -1.33 | LF | 34.1.1 | ? | FAO, 1984 (p 5) | URSS |
? | 40.88 | 0.22 | -1.31 | LF | 34.1.3 | ? | FAO, 1984 (p 5) | URSS |
1972–82 | 38.98 | 0.2775724 | -1.1613564 | LF | SEN-MAURIT | ? | FAO, 1984 (p 5) | ROUMANIE |
? | 61.36 | 0.1011 | -0.85 | ? | MAROC | OTOLITHES | FAO, 1984 (p 129) | MAROC |
? | 53.3 | 0.12 | -0.3 | ? | MAROC | OTOLITHES | FAO, 1984 (p 130) | MAROC |
1978–79 | 43.39 | 0.19 | -1.31 | ? | MAROC | ? | FAO, 1984 (p 130) | MAROC |
1981 | 60.03 | 0.0854 | -3.734 | 25-LT-42 | MAURITANIE | OTOLITHES | HOFFMANN, 1987 | RDA |
1982 | 46.34 | 0.1877 | -1.463 | 20-LT-41 | MAURITANIE | OTOLITHES | HOFFMANN, 1987 | RDA |
1983 | 36.06 | 0.357 | -0.475 | 17-LF-39 | MAURITANIE | OTOLITHES | HOFFMANN, 1987 | RDA |
1984 | 45.82 | 0.2006 | -1.02 | 14-LF-39 | MAURITANIE | OTOLITHES | HOFFMANN, 1987 | RDA |
1982 (1° trim) | 51.863 | 0.1574 | -1.61 | 27-LT-40 | MAURITANIE | OTOLITHES | HOLZLOHNER & AL, 1983 | RDA |
1982 (2° trim) | 48.423 | 0.2322 | -1.026 | 21-LT-37 | MAURITANIE | OTOLITHES | HOLZLOHNER & AL, 1983 | RDA |
1982 (4° trim) | 40.248 | 0.4758 | 0.09 | 25-LT-41 | MAURITANIE | OTOLITHES | HOLZLOHNER & AL, 1983 | RDA |
TRACHURUS TRECAE | Paramètres de croissance | | |
ANNEE | LINFINI | K | tO | GAMME DE TAILLE(cm) | ZONES | METHODES | SOURCES | NATIONALITE |
1973–76,81,82 | 41.75 | 0.2166723 | -1.403 | 10-LF-42 | 16–26°N | OTOLITHES | FAO, 1984 (p 53) | ROUMANIE |
1981 | 41.9 | 0.345 | -1.098 | 14-LT-41 | MAURITANIE | OTOLITHES | FAO, 1984 (p 8) | RDA |
? | 50.2 | 0.22 | -0.59 | LF | 34.1.3 | OTOLITHES | FAO, 1984 (p 8) | URSS |
? | 58.08 | 0.15 | -0.66 | LF | 34–3.1.(Gui. B) | OTOLITHES | FAO, 1984 (p 8) | URSS |
1982 (1°trim) | 98.805 | 0.0519 | -4.275 | 19-LT-37 | MAURITANIE | OTOLITHES | HOLZLOHNER & AL, 1983 | RDA |
1982 (2°trim) | 45.588 | 0.2591 | -1.161 | 24-LT-44 | MAURITANIE | OTOLITHES | HOLZLOHNER & AL, 1983 | RDA |
1982 (3°trim) | 43.78 | 0.3449 | 0.496 | 21-LT-45 | MAURITANIE | OTOLITHES | HOLZLOHNER & AL, 1983 | RDA |
1982 (4°trim) | 45.287 | 0.3168 | -1.431 | 19-LT-49 | MAURITANIE | OTOLITHES | HOLZLOHNER & AL, 1983 | RDA |
1984–85 | 38.45 | 0.257 | -0.843 | 14-LF-33 | SENEGAL | EPINE DORS. | CAMARENA, 1986 | SENEGAL |
DECAPTURUS RHONCHUS Reproduction |
AIRE DE PONTE | PERIODE MAXIMUMPROFOND | TEMPERA DE PONTE | TAILLE DE MATURITE (cm) | SEX-RATIO FEM/MALES | FECONDITE | SOURCES | NATIONAL |
DEPONTE | (m) | OPTIMALE |
SENEGAL | AVR–NOV | MAI–JUIN | | 15–29°C | | | | CONAND & FRANQUEV., 1973 | |
17–22°N | JUIL–SEPT | | | | | 1.4 | | MAXIM & STAICU, 1976 | ROUMAN |
9°30–9°45N | AVR–JUIL | JUIL | | 18.7° | (2ans) | | 480–990000 | FAO, 1979 (p127) | URSS |
16–21°N | JUIN–JUIL | MAI–JUIL | | | 18.5 | | | FAO, 1984 (p12) | URSS |
SENEGAL | AVR–NOV | MAI–JUIN | | | 20–21 | | | FAO, 1984 (p12) | SENEGA |
SENEGAL | MAI–JUIN | | | | 20 | 1.3 | | CAMARENA, 1986 | SENEGA |
MAURITANIE | AVR–AOUT | AVR–AOUT | | | 19.4 | 1.13 | | LAWAL & MYLNIKOV, 1988 | MAURITA |
SCOMBER JAPONICUS Reproduction |
AIRE DE PONTE | PERIODE MAXIMUMPROFOND | TEMPERA OPTIMALE | TAILLE DE MATURITE (cm) | SEX-RATIO FEM/MALES | FECONDITE | SOURCES | NATIONAL |
DE PONTE | DE PONTE | (m) |
24–25°30N | JANV–MARS | | | 17.2–22.2°( | 31(LT) | | | FAO, 1979 (p 13) | URSS |
22°30N | | | | | | | | | |
10–15°N | DEC–FEV | DEC | 180–200 | 17.2–22.2°( | 27.5 | | | FAO, 1979 (p13) | URSS |
MAURITANIE | DEC–MARS | | | 31(LT) | | | | FAO, 1984 (p15) | URSS |
34.1.3 | MARS–MAI | | | | 25.7 | | | FAO, 1984 (p15) | URSS |
34.3.1 | DEC-MAI | | | | 22.2 | | | FAO, 1984 (p15) | URSS |
SEN-MAURITANIE | JANV-MARS | | | | 24–36 | | | FAO, 1984 (p15) | ROUMANIE |
| | | | | | | 1)90–250000 | FAO, 1987 (p19) | ? |
| | | | | | | 2)190–248000 | FAO, 1987 (p19) | ? |
SENEGAL | | | | | | 22#1.4 | | CAMARENA, 1986 | SENEGAL |
MAURITANIE | NOV–FEV | NOV–JANV | | | | 24.6 | 1.24 | LAWAL & MYLNIKOV, 1988 | MAURITAN |
SARDINELLA MADERENSIS Reproduction |
AIRE DE PONTE | PERIODE MAXIMUM PROFOND | TEMPERA OPTIMALE | TAILLE DE MATURITE (cm) | SEX-RATIO FEM/MALES | FECONDITE | SOURCES | NATIONAL |
DE PONTE | DEPONTE | (m) |
SENEGAL | Tte l'année | MAI–JUIL | | | | | | FAO, 1979 (p8) | SENEGAL |
SENEGAL | | JUIL-AOUT | | | | | | | |
| | (variable) | | | 16.5 | | | BOELY, 1979 | SENEGAL |
SENEGAL | | MAI–JUIL | | | | | | | |
| | NOV–DEC | | | 16 | 12 | | CAMARENA, 1986 | SENEGAL |
MAURITANIE | MARS–AOU | MAI–AOUT | | | | 1.56 | | LAWAL & MYLNIKOV, 1988 | MAURITAN |
SARDINELLA AURITA Reproduction |
AIRE DE PONTE | PERIODE MAXIMUMPROFOND | TEMPERA OPTIMALE | TAILLE DE MATURITE (cm) | SEX-RATIO FEM/MALES | FECONDITE | SOURCES | NATIONAL |
DE PONTE | DEPONTE | (m) |
19–20°N | MARC–OCT | MAI–AOUT | 80 – 110 | | | | | FAO, 1979(p18) | URSS |
13–17°N | Tte l'année | MAI–AVR | 50 – 80 | 8.4 – 19.8°( | 22 | | | FAO, 1979 (p18) | URSS |
8–10°N | JANV–MAI | SEPT–OCT | 10–40 | | 14 | | | FAO, 1979 (p18) | URSS |
| AOUT–NOV | | | | | | | | |
SEN-MAURITAN | Tte l'année | JUIL-SEPT | | | 20 | | 400w/gr(SEN) | FAO, 1979 (p18) | SENEGAL |
| déplac du foy | VIAI:Gambie | | | | | 49600–133800 | | |
| de reproduc | SEP:C.Blanc | | | | | (28 – 40 cm) | | |
SENEGAL | AVR–JUIN | | | | 18.5 | 1 | | BOELY & AL, 1982 | SENEGAL |
| OCT–NOV | | | | | | | | |
SENEGAL | MAI–JUIN | | | | 18 | 1 | | | |
MAURITANIE | | AVR–SEP | | | | 1.48 | | LAWAL & MYLNIKOV, 1988 | MAURITAN |
SARDINELLA AURITA Reproduction |
AIRE DE PONTE | PERIODE MAXIMUM PROFOND | TEMPERA OPTIMALE | TAILLE DE MATURITE (cm) | SEX-RATIO FEM/MALES | FECONDITE | SOURCES | NATIONALI |
DE PONTE | DE PONTE | (m) |
20.21°N(princ.) | | | | | | | | | |
18°30–19.30N (secondaire) | SEP.AVR | DEC. | 110–300 | 15–16°C | 21 | 1 | 115–127000 | FAO. 1979(p. 9) | URSS |
14–16°N | DEC–MAI | JAN | 110–300 | 15–16°C | 16 | | 115–127000 | FAO. 1979(p.9) | URSS |
SEN-MAURIT. | OCT–MAI | DEC–FEV | | 15–18°C | 19.7 | 1 | 22–346000 | FAO, 1984(p.6) | URSS |
zone dépendant des migratiońs | | | | | 18.05 | 1 | (n=120000) | | |
MAURITANIE | NOV–AVR | NOV–JAN | | | 19.3 | 1.32 | | LAWAL & MYLINIKOV, 1988 | MAURITAN |
TRACHURUS TRECAE Reproduction |
AIRE DE PONTE | PERIODE MAXIMUM PROFOND | TEMPERA OPTIMALE | TAILLE DE MATURITE (cm) | SEX-RATIO FEM/MALES | FECONDITE | SOURCES | NATIONAL |
DE PONTE | DE PONTE | (m) |
13–19°N | FEV–MAI | | | | | | | BOELLY & AL., 1973 | |
21–22°N | SEP–AVR | FEV–AVR | 100–150 | 18.5–25.5°C | 31.5 | | 151–772700 par ponte | FAO, 1979 (p.10) | URSS |
15–19°N | SEP–AVR | FEV–AVR | 100–150 | 18.5–25.5°C | 16.8 | | | FAO, 1979 (p.10) | URSS |
11°30–14°N | SEP–AVR | FEV–AVR | 100–150 | 17.5–25.5°C | 12.5 | | | FAO, 1979 (p.10) | URSS |
15–21°N | OCT–FEV | | | | 28–30 | | | FAO, 1979 (p.9) | RDA |
15–26°N | SEP–MAR | | | | 24.3 | | | FAO, 1979 (p.9) | URSS |
SENEGAL | FEV–AVR | | | | 18 | | | FAO, 1979 (p.9) | SENEG |
MAURITANIE | DEC–AVR | | | | 19.56 | | | FAO, 1979 (p.9) | ROUMAN |
MAURITANIE | DEC–JUIL (tte l'année) | JAN–AOU | | | 23 | 1.1 | | LAWAL & MYLNIKOV, 1988 | MAURITAN |
SENEGAL | FEV–MAI | | | | 20 | 1.4 | | CAMARENA, 1986 | SENEGA |
FACTEUR DE CONVERSION LONGUEUR FOURCHE/LONGUEUR TOTALE
ESPECE | EQUATION | SOURCES | NATIONALITE |
TRACHURUS TRACHURUS | LF=LT×0.897 | HOLZLOHNER & KLOXIN, 1985 | RDA |
TRACHURUS TRECAE | LF=LT×0,879 | HOLZLOHNER & KLOXIN, 1985 | RDA |
DECAPTERUS RHONCHUS | LF=LT×0,882 | HOLZLOHNER & KLOXIN, 1985 | RDA |
SCOMBER JAPONICUS | LF=LT×0,928 | HOLZLOHNER & KLOXIN, 1985 | RDA |
| LF=0,866 LT + 1,9 | FAO, 1984 (p15) | URSS |
| 1.F=0,8829 LT + 1,12591 | FAO, 1984 (p15) | RDA |
SARDINELLA AURITA | LF=LT×0,843 | HOLZLOHNER & KLOXIN, 1985 | RDA |
| 1.T=1,21 LF - 0,857 | BOELY & AL, 1982 | SENEGAL |
SARDINELLA MADERENSIS | LF=LT×0,843 | HOLZLOHNER & KLOXIN, 1985 | RDA |