Journal of Applied Ichthyology J. Appl. Ichthyol. 27 (Suppl. 3) (2011), 56–59 2011 Blackwell Verlag, Berlin ISSN 0175–8659 Received: November 21, 2010 Accepted: April 17, 2011 doi: 10.1111/j.1439-0426.2011.01853.x Short communication First report on the status of Allis shad (Alosa alosa) in the Minho River (Northwestern Iberian Peninsula) By M. Mota1,2,3 and C. Antunes2,3,4 1 ICBAS – Institute of Biomedical Sciences of Abel Salazar, University of Porto, Porto, Portugal; 2CIMAR ⁄ CIIMAR – Interdisciplinary Centre of Marine and Environmental Research, University of Porto, Porto, Portugal; 3Aquamuseu do Rio Minho, Parque do Castelinho, Vila Nova de Cerveira, Portugal; 4ESG - Escola Superior Gallaecia, Largo das Oliveiras, Vila Nova de Cerveira, Portugal Introduction The Allis shad (Alosa alosa Linnaeus 1758) is an anadromous member of the family Clupeidae. Like other diadromous fish (see Limburg and Waldman, 2009), this species has been progressively disappearing from European rivers due to river fragmentation, increasing sediment load and pollution. In Portugal a marked decline in the shad populations was noticed since the middle of the 20th century, particularly in the rivers Minho and Lima, while in the rivers Tagus and Guadiana only a residual population still exists (Faria, 2007). The anthropogenic pressures that seem to cause the gradual disappearance of A. alosa in several European basins, has resulted in its listing in (i) the Red List of the International Union for the Conservation of the Nature (IUCN), (ii) in Annex III of the Bern Convention, and in the Habitats Directive. The drastic decline in the spawning stock biomass and the restrictions of usable habitat area prompted its classification at national level as a species in danger (Cabral et al., 2006), now being under legal protection. As other Portuguese rivers (Lima, Cávado, Douro, Vouga, Mondego, Tejo, Sado and Guadiana), the Minho was one of the rivers with the highest catches of the species (Baldaque da Silva, 1892) and, in the Minho River basin, A. alosa still has a great commercial and cultural value. Portuguese official statistics of the small-scale fishery confirm mean catches of 200 tonnes during the first half of the 20th century, with peaks of 300 tonnes. After the 1950s catches decreased by about 90% (Fig. 1), coinciding with the construction of the first dam (Alexandrino, 1996; Baglinière et al., 2003). In the last 20 years mean annual catches reached about four tonnes, while in 1980 the catch peaked with about 18 tonnes. However, these values seem to be underestimates due to the lack of good official statistics and unofficial Portuguese and Spanish data over the last eight years indicates that yields may have been twice as high, pointing to the existence of a noticeable population worth studying to develop conservation and restoration strategies. Furthermore, this species has become rare in Southern Europe (Limburg and Waldman, 2009). The objectives of this study, therefore, were to identify key parameters of the general biology of the species in the Minho River and assess the actual state of the Alosa alosa population in this specific river. Material and methods Specimens were sampled by experimental fishing and from fishermen of the international part (Spain and Portugal) of the Minho River between April and August 2009. Two sampling stations (estuary and spawning area) were selected (Fig. 2). A typical trammel net (140 m long; 140 mm loose inner layer mesh size) was used. Fig. 1. Time series data for half a century of A. alosa catches (kg and numbers) in the Minho River reported by Portuguese fishermen to the local Maritime AuthoritiesAuthority of Fishing Port of Caminha Status of Allis shad (Alosa alosa) in the Minho River 57 Results and discussion Fig. 2. Map of the study area showing the location of the two experimental fishing sites (w) Total length (TL) was measured to the nearest 0.1 cm (measuring board) and total weight (TW) was determined to the nearest 5 g (digital hanging Kern HDB balance). The TL and TW statistics were expressed as means and standard deviations, separately according to sex, as well as the respective maximum and minimum values. Gonads were removed from both sexes and weighed using a digital A&D EK-610i balance with a precision of 0.01 g. The gonadosomatic index (GSI) was calculated for each sex in order to document changes in fish maturity and spawning state during the upstream migration, using the equation GSI = 100*(Wg ⁄ Wt) where Wg is the gonad weight (g) and Wt is the fish total weight (g). Condition factors with gonad weight (K) and without gonad weight (K¢) and gonadal factor condition (DK) were estimated as K ¼ 100 ðWt =Lbt Þ; K 0 ¼ 100 ðWc =Lbt Þ; DK = K)K¢ where Wt is the fish total weight (g), Wg is the gonad weight (g), Wc = Wt)Wg; Lt is the total length (cm) and b is the allometric coefficient obtained through the length-weight relationship. Scales of 111 specimens were removed and treated according to Baglinière et al. (2001) for ageing and identification of spawning marks. The available habitat for the A. alosa in the Minho River during freshwater migration covers a stretch of approximately 80 km in the international Minho River section (from the estuary to the first dam). Their estuary upstream migration began in March and ended in June. The earlier spring migration is related to the latitude: south populations migrate earlier in the year than further north populations (MennessonBoisneau et al., 2000a; Aprahamian et al., 2002; Baglinière et al., 2003). The highest percentage of males occurred in March and April (63.6 and 69.6% respectively), while females dominated May and June (61.2 and 80%, respectively). This migratory behaviour is in accordance with the life history described for this species (Baglinière et al., 2003; Maitland and Hatton-Ellis, 2003), where males migrate upstream first, followed by females. The presence of post-spawner shads in the upper international Minho River, in early August, may suggest the spawning season to extent until this month, as reported for other A. alosa populations (Baglinière et al., 2003). From the total samples, 49.5% were females and 50.5% were males, indicating no significant difference (P > 0.05) from a 1 : 1 sex ratio as also described for the Douro River A. alosa population (Eiras, 1981). However, other A. alosa populations showed different sex ratios (Table 1) and it seems difficult to explain whether annual fluctuations of this parameter reflects a biological principle or represent a bias in the sampling methods, periods and ⁄ or locations (MennessonBoisneau et al., 2000b). The results on biometrical and demographical structure of the 200 specimens sampled are given in Table 1 and Fig. 3. Comparing with northern populations, the Minho River A. alosa population presents the highest growth rate. This pattern was also demonstrated by Lassalle et al. (2008), where comparisons of Portuguese and Moroccan populations with northern population showed larger lengths to the first ones (negative latitudinal gradient). In contrast, allometric coefficient b was lowest than in the Portuguese and Moroccan populations considered by Mennesson-Boisneau et al. (2000b). However, the Douro River population (Froese and Pauly, 2005) showed an allometric coefficient close to the one given for the Minho River population. Although the Minho and Table 1 Total length and weight results for the Minho River A. alosa L. sampled between March and July 2009 and comparison with European and Moroccan populations (adapted to Mennesson-Boisneau et al., 2000b) Minho River (present study) Females Males b 2.81 (mixed) N 99 101 % 49.5 50.50 Length (mm) X 664 607 SD 34 25 Min 540 530 Max 740 670 Weight (g) X 2678 2208 SD 819 408 Min 915 890 Max 4355 3450 Lima River (Alexandrino, 1996) Females Males 3.1139 (mixed) 86 97 47 53 Loire River (MennessonBoisneau, 1990) Gironde River (Taverny, 1991) Adour River (Prouzet, unpublished data) Sebou River (Sabatié 1993) Females Males Females Males Females Males Females Males 3.019 1041 47 3.114 1172 53 3.3429 191 56 3.2252 152 44 2.671 101 46 3.116 118 54 3.4105 317 40 3.2587 482 60 636 3.8 490 720 549 4.4 445 670 634 44 480 733 537 61 400 666 556 39 414 680 484 39 339 635 585 26 509 650 533 29 383 597 539 25 475 600 492 32 415 605 2864 611 1237 4400 1663 575 668 3215 1712 489 500 3800 1067 342 174 2487 2185 391 1245 3250 1572 299 610 2775 2066 329 1400 2900 1411 324 800 2800 3019 58 1250 4525 N, n of individuals; b, allometric coefficient; %, percentage; X , average; SD, standard deviation; Min, minimum and Max, maximum. 1800 47 850 3275 58 M. Mota and C. Antunes Fig. 5. Variation in the Gonadal factor condition (DK) of males and females of Alosa alosa during the months of the spawning migration in the Minho River Fig. 3. Length-weight relationship for the A. alosa population migrating for spawning into the Minho River. The allometric equation is given as: W = total weight (g), L = total length (cm); a = 0.0221 and b = 2.8147. Data are combined for both sexes. The low b value may have been caused by spent fish Table 2 Age structure of Minho River A. alosa population by sex and length Males Douro populations are larger in length, they present lower weights compared to length-weight relationships to the rest of the populations elsewhere and thus may explain the difference. GSI revealed highest values for females and, with the exception in April when we observed a slight decrease in the GSI values. GSI increased until June and strongly decreased in July for both sexes, indicating an increase of gonadal weight during the upstream migration and the presence of postspawners in July (Fig. 4). Condition factor (K) decreased along the five migratory months for both sexes. In contrast, gonadal condition factor (DK) was the same from March to May and slightly decreasing in June and July for males and, for the females, slightly decreased from March to April, rose from May to June, and fell again in July (Fig. 5). The high female (DK) observed in June indicates fish are ready to spawn. The age structure of migratory adults is given in Table 2. The scales reading revealed an average age of 6.7 years for the total fish sampled. For males, 57.4% of the specimens were 6 years old and 58.1% of females were 7 years old. As seen in other studies (Mennesson-Boisneau et al., 2000b; Aprahamian et al., 2002; Lassalle et al., 2008) the majority of females matured one year later than males, however, the majority of the Minho River adults spawner population seems to be one Females Length (mm) Age N % 5 6 7 8 7 58 36 – 6.93 57.4 35.66 – X 604,3 604.7 614.6 – Length (mm) SD N % 35.64 23.53 21.66 – 2 9 54 28 2.15 9.68 58.06 30.11 X 620.0 655.6 663.1 667.3 SD 84.85 17.40 35.89 33.95 N, sample size; %, percentage; X , average; SD, standard deviation. year older than those of other European and Mediterranean populations. Further, 5.4% of the spawners had spawning marks on their scales. These results show the evidence of a few fish returning for a second spawning migration and thus, as other European populations (see Mennesson-Boisneau et al., 2000b; Aprahamiam et al., 2002; Maitland and Hatton-Ellis, 2003), this population is considered semelparous. In the last 30 years two peaks were revealed concerning the data of Portuguese fishermen (1980 and 2009 spawning seasons). Although fluctuations in the abundance of Alosa populations are a reality (Baglinière et al., 2003), future investigations will be carried out in the way of enhance knowledge of the status and dynamic of the Minho River A. alosa population. Acknowledgements Micaela Mota is supported by a PhD grant from the Portuguese Foundation for Science and Technology – FCT (SFRH ⁄ BD ⁄ 44892 ⁄ 2008). Special thanks to Eduardo Martins, Eugénio Pereira and Dr. Ronaldo Sousa for the field assistance, Vânia Gonçalves, Cátia Patrão and Rita Carvalho for the laboratory assistance and to the fishermen concerning biological samples and to Eng. Claudio Ramos for the study area map arrangement. Conflict of interests Fig. 4. Changes of the Gonadossomatic Index (%) (GSI) in A. alosa specimens during the spawning upstream migration in the Minho River, shown separately for males and females. Total n = 200 specimens The authors have no conflict of interest to declare and note that the sponsors of the issue had no role in the study design, data collection and analysis, decision to publish, or preparation of the manuscript. Status of Allis shad (Alosa alosa) in the Minho River References Alexandrino, P., 1996: Estudo de populações de Sável (Alosa alosa L.) e Savelha (Alosa fallax Lacepède). Análise da diferenciação interespecı́fica, subestruturação e hibridação. (Study of Allis shad (Alosa alosa) and Twaite shad (Alosa fallax). Analysis of interspecific differentiation, substructure and hybridization). PhD thesis. Faculty of Sciences, University of Porto, Portugal, pp. 185. Aprahamian, M. W.; Baglinière, J. L.; Sabatié, M. R.; Alexandrino, P.; Aprahamian, C. 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In: Les aloses Alosa alosa et Alosa fallax spp. (The alosines Alosa alosa and Alosa fallax). J. L. Baglinière and P. Elie (Eds). INRA-Cemagref, Paris, France, pp. 55–72. Mennesson-Boisneau, C.; Aprahamian, M. W.; Sabatiè, M. R.; Cassous-Leins, J. J., 2000b: Caractéristiques des adultes (Adults characteristics). In: Les aloses Alosa alosa et Alosa fallax spp. (The alosines Alosa alosa and Alosa fallax). J. L. Baglinière and P. Elie (Eds). INRA-Cemagref, Paris, France, pp. 33–53. AuthorÕs address: Micaela Mota, Várzea – Parada, 4940-441 Paredes de Coura, Portugal. E-mail: [email protected]