Observations on the ecology of a landlocked population of allis shad in Aguieira Reservoir, Portugal

A landlocked population of the anadromous clupeid Alosa alosa from Aguieira Reservoir in Portugal is described. The individuals are fast-growing, mature in their third year of life, live for 5+ years, and consequently spawn more than once.     

Factors related to gizzard shad and the threadfin shad occurrence and abundance in Florida lakes

Gizzard shad Dorosoma cepedianum were collected in 23 and threadfin shad D. petenense were collected in 22 of the 60 Florida lakes sampled. Logistic regression equations were 94% effective for predicting gizzard shad occurrence from chlorophyll and lake surface area, and 84% effective for predicting threadfin shad occurrence from lake surface area and lake volume inhabited (PVI). Occurrence of both shad species was related positively to lake size. In lakes where gizzard shad or threadfin shad were collected, shad density and biomass of both shad species were related positively to chlorophyll. Gizzard shad populations were generally vulnerable to predation in lakes, with the per cent of gizzard shad ≤200mm L _T values exceeding 60% with few exceptions. Effects of gizzard shad and threadfin shad on fish community dynamics may be confined to relatively large (>100 ha) and fertile (chlorophyll >20–30μg l⁻¹) Florida lakes.     

Does global warming impact on migration patterns and recruitment of Allis shad (<Emphasis Type="Italic">Alosa alosa</Emphasis> L.) young of the year in the Loire River,France?

The hydrological and thermal changes in the Loire River were investigated to test the influence of climatic changes on a short freshwater stage anadromous fish species, Allis shad, for the 1995–2004 period. The mean water temperatures during the adult migration and juvenile growth phases showed significant increase, and mean water flow during these two phases decreased significantly. The period below the threshold of 18°C shortened, and the period between 18°C and the maximum lengthened, while the temperature amounts (number of degree-days) received by aquatic organisms between 18 and 24°C showed an increase. The pattern of young-of-the-year downstream migration was modified. The first day when the juvenile catches reached 5% occurred 17 days earlier at the end of the 1995–2004 period than at the beginning. The first day when the juvenile catches reached 50% was related to the 18°C threshold (reproductive threshold) and the temperature amounts accumulated between the 18 and 20°C thresholds. The year-on-year levels of young-of-the-year abundance showed wide variations, which were not explained by environmental parameters, probably because of the long distance between the study site and the spawning grounds.

Return of twaite shad <Emphasis Type="Italic">Alosa fallax</Emphasis> (Lacépède, 1803) to the Southern Baltic Sea and the transitional area between the Baltic and North Seas

The status of twaite shad was investigated within the Southern Baltic Sea (ICES subdivision 22–27) and transitional area between the Baltic and North Seas (division IIIa). The following sources of data were analysed: (i) commercial catch statistics and relevant publications, (ii) records from ichthyological museum collections, (iii) records from recent commercial and recreational fisheries, (iv) research fisheries with trawls. A total of 476 records of twaite shad including more than 16 million individuals were obtained for the time between the years 1836 and 2005. About 72.9% of all records originated from commercial catch statistics and publications, whereas 18.9% were received from ichthyological collections. Research fisheries provided 6.3%, and 1.9% of the records were obtained from recent commercial and recreational fisheries. Most records of twaite shad were estimated for subdivisions 24 (45.2%) and 26 (35.5%). From 1836 to 1959, 29.6% of the records date from the period until 1899. 70.4% of the records of twaite shad originate from the twentieth century until 1959. The mean annual catch of twaite shad between 1891 and 1959 amounted to 86,674 kg within subdivisions 24–26 of the Southern Baltic Sea. Catch data show an approximately 20-year-cyclicity of maximum yields and minimum catches, respectively. The maximum annual yield of twaite shad in subdivisions 24–26 (474,700 kg) was registered in 1940, the minimum annual yield was estimated in 1958 (10 kg). In the 1950s, the annual catches of twaite shad declined sharply. Until 1960 twaite shad catches and records originated mainly from the Pommeranian Bay/Pommeranian Coast and adjacent waters including the Szczecin Lagoon (subdivision 24), the Bay of Gdańsk, Vistula Lagoon and Vistula Spit (subdivision 26) and from the Curonian Lagoon and Curonian Spit (subdivision 26). The highest catches of twaite shad originated from the area of Curonian Lagoon/Curonian Spit from 1941 to 1960. Seasonal catches of twaite shad showed maximum values from May to July. From 1960 to 1989, only four records of A. fallax were registered in the Southern Baltic Sea which originated from German coastal waters in subdivisions 22 and 24. A total of 107 records of twaite shad was obtained in subdivisions 20–27 from 1990 to 2005. Most of these recent records originate from a twaite-shad stock in subdivisions 24, 25 and 26. There are indications which suggest a separate stock of twaite shad in subdivisions 20 and 21. Disappearance and recovery of twaite shad stocks were probably caused by the following factors: construction of barriers in rivers with spawning sites of twaite shad; habitat destruction in those rivers as consequence of gravel extraction and reengineering scheme to improve navigation and for flood defence purposes, water pollution in the lagoons of the Southern Baltic and in their tributaries, commercial fishery in the Southern Baltic and climatic variation in the Baltic Sea basin south of the latitude of 60° N. Electronic supplementary material The online version of this article (doi:) contains supplementary material, which is available to authorized users. Guest editors: S. Dufour, E. Prévost, E. Rochard & P. Williot Fish and diadromy in Europe (ecology, management, conservation)     

Fish gut microbiota analysis differentiates physiology and behavior of invasive Asian carp and indigenous American fish

Gut microbiota of invasive Asian silver carp (SVCP) and indigenous planktivorous gizzard shad (GZSD) in Mississippi river basin were compared using 16S rRNA gene pyrosequencing. Analysis of more than 440 000 quality-filtered sequences obtained from the foregut and hindgut of GZSD and SVCP revealed high microbial diversity in these samples. GZSD hindgut (GZSD_H) samples (n=23) with >7000 operational taxonomy units (OTUs) exhibited the highest alpha-diversity indices followed by SVCP foregut (n=15), GZSD foregut (n=9) and SVCP hindgut (SVCP_H) (n=24). UniFrac distance-based non-metric multidimensional scaling (NMDS) analysis showed that the microbiota of GZSD_H and SVCP_H were clearly separated into two clusters: samples in the GZSD cluster were observed to vary by sampling location and samples in the SVCP cluster by sampling date. NMDS further revealed distinct microbial community between foregut to hindgut for individual GZSD and SVCP. Cyanobacteria, Proteobacteria, Actinobacteria and Bacteroidetes were detected as the predominant phyla regardless of fish or gut type. The high abundance of Cyanobacteria observed was possibly supported by their role as the fish''s major food source. Furthermore, unique and shared OTUs and OTUs in each gut type were identified, three OTUs from the order Bacteroidales, the genus Bacillariophyta and the genus Clostridium were found significantly more abundant in GZSD_H (14.9–22.8%) than in SVCP_H (0.13–4.1%) samples. These differences were presumably caused by the differences in the type of food sources including bacteria ingested, the gut morphology and digestion, and the physiological behavior between GZSD and SVCP.     

Effect of threadfin shad density on production of threadfin shad and gizzard shad larvae in a Tennessee reservoir

Production of larvae by threadfin shad, Dorosoma petenense, and gizzard shad, D. cepedianum, varied over two orders of magnitude and was regulated by adult threadfin shad abundance over five years in Normandy Reservoir, Tennessee. Significantly more larvae of both species were produced in years following winterkills of threadfin shad (repeated-measures ANOVA, df=4, 75; F > 21.44, p=0.0001). Peak geometric mean catch of threadfin shad larvae in neuston samples was inversely related to biomass (kg ha^–1; r = – 0.91; p=0.031) and density (no. ha^–1; r=– 0.89; p = 0.043) of adult (> 70 mm total length) threadfin shad in mid-summer cove samples. Peak geometric mean catch of gizzard shad larvae was also inversely related to adult threadfin shad biomass (r = – 0.93; p=0.022) and density (r=– 0.88; p=0.046) in cove samples. Winterkills of threadfin shad were size selective, killing all fish under 60 mm total length but allowing some unknown percentage of larger fish to survive. When threadfin shad stocks were reduced by winterkills, surviving threadfin shad and gizzard shad may have taken advantage of less competition for food resources in early spring and increased condition enough to spawn successfully.     

Homing behaviour facilitates subtle genetic differentiation among river populations of Alosa sapidissima: microsatellites and mtDNA

Significant but subtle differentiation was detected for both microsatellite DNA and mitochondrial DNA among four populations of American shad Alosa sapidissima . The data indicate that straying among rivers is sufficient to permit only marginal population differentiation in this species, but suggest that individual river populations should be managed as distinct stocks. Comparison of the Hudson and Columbia populations, the latter derived from the former over 100 years ago, revealed only a slight reduction in microsatellite DNA variation for the founded population but halving of mitochondrial DNA, consistent with the haploid maternal inheritance of the latter marker. The depleted and endangered James River (Virginia) population and two other Atlantic coast populations exhibited similar levels of microsatellite DNA variation, but mtDNA diversity in the James River was marginally lower than in other Atlantic populations, again consistent with the low effective population size of mtDNA.     

Genetic diversity and differentiation in a wide ranging anadromous fish,American shad (Alosa sapidissima), is correlated with latitude

Studies that span entire species ranges can provide insight into the relative roles of historical contingency and contemporary factors that influence population structure and can reveal patterns of genetic variation that might otherwise go undetected. American shad is a wide ranging anadromous clupeid fish that exhibits variation in demographic histories and reproductive strategies (both semelparity and iteroparity) and provides a unique perspective on the evolutionary processes that govern the genetic architecture of anadromous fishes. Using 13 microsatellite loci, we examined the magnitude and spatial distribution of genetic variation among 33 populations across the species' range to (i) determine whether signals of historical demography persist among contemporary populations and (ii) assess the effect of different reproductive strategies on population structure. Patterns of genetic diversity and differentiation among populations varied widely and reflect the differential influences of historical demography, microevolutionary processes and anthropogenic factors across the species' range. Sequential reductions of diversity with latitude among formerly glaciated rivers are consistent with stepwise postglacial colonization and successive population founder events. Weak differentiation among U.S. iteroparous populations may be a consequence of human‐mediated gene flow, while weak differentiation among semelparous populations probably reflects natural gene flow. Evidence for an effect of reproductive strategy on population structure suggests an important role for environmental variation and suggests that the factors that are responsible for shaping American shad life history patterns may also influence population genetic structure.