Oogenesis in fishes follows a universal plan; yet, due to differences in the synchrony and rate of egg development, spawning frequency varies from daily to once in a lifetime. Some species spawn and feed in separate areas, during different seasons, by storing energy and drawing on it later for reproduction (i.e. capital breeding). Other species spawn using energy acquired locally, throughout a prolonged spawning season, allocating energy directly to reproduction (i.e. income breeding). Capital breeders tend to ovulate all at once and are more likely to be distributed at boreal latitudes. Income breeding allows small fish to overcome allometric constraints on egg production. Income breeders can recover more quickly when good‐feeding conditions are re‐established, which is a benefit to adults regarding bet‐hedging spawning strategies. Many species exhibit mixed capital‐ and income‐breeding patterns. An individual's position along this capital–income continuum may shift with ontogeny or in relation to environmental conditions, so breeding patterns are a conditional reproductive strategy. Poor‐feeding environments can lead to delayed maturation, skipped spawning, fewer spawning events per season or fewer eggs produced per event. In a few cases, variations in feeding environments appear to affect recruitment variability. These flexible processes of energy acquisition and allocation allow females to prioritize their own condition over their propagules' condition at any given spawning opportunity, thereby investing energy cautiously to maximize lifetime reproductive value. These findings have implications for temporal and spatial sampling designs, for measurement and interpretation of fecundity, and for interpreting fishery and ecosystem assessments.

Gibel carp Carassius gibelio (Bloch) was first introduced into fish ponds and small lakes of Estonia in 1948-49, and first detected in Estonian brackish waters (Gulf of Riga) in 1985.Since the mid-1990s, the species has spread along the entire Estonian Baltic coastline. Growth rate in the brackish water population does not differ much from freshwater populations, but the freshwater populations are gynogenetic (or show high dominance of females) in contrast to the Baltic Sea population, which presents a normal sex ratio. The recent explosion of this species in the Baltic Sea could be explained by unusually warm summers during the 1990s and by the low abundance of predatory fish.

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Vetemaa, M., Eschbaum, R., Albert, A., Saks, L., Verliin, A., Jürgens, K., Kesler, M., Hubel, K., Hannesson, R., and Saat, T. 2010. Changes in fish stocks in an Estonian estuary: overfishing by cormorants? – ICES Journal of Marine Science, 67: 1972–1979. In Estonia, the cormorant Phalacrocorax carbo sinensis is a newcomer, and its numbers have increased rapidly since 1985. In the shallow protected (no fishery) Käina Bay in Väinameri (West Estonia), the colony was established in 1995. Gillnet sampling indicated that roach was the most abundant spawning fish species in 1995. Ten years later, when the study was repeated, the catch per unit effort was already more than 100 times lower than in 1995. The number of spawning perch decreased tenfold from 1995 to 2005. During the same period, commercial fishing effort in the entire Väinameri area decreased several times. The change in fish abundance in the Käina Bay and in the coastal fish-monitoring areas in the archipelago sea nearby, together with an analysis of food of cormorants, indicates that the decline in fish abundance might be related to the increased numbers of cormorants. The conclusion is drawn that the establishment of a cormorant colony could have seriously damaged or even prevented normal functioning of historically important spawning grounds and affected fish recruitment to adjacent areas. Therefore, expanding bird colonies might play a role similar to an expanding fishing fleet, by overexploiting the resource.

–  Matsalu Bay in the Väinameri (West‐Estonian Archipelago Sea) is a relatively shallow but large bay. It is the only real delta estuary in the northern Baltic Sea. The fish fauna is strongly dominated by freshwater species such as perch Perca fluviatilis, roach Rutilus rutilus, white bream Blicca bjoerkna and rudd Scardinius erythrophthalmus. The study presents CPUE data describing annual and seasonal variations in the species composition, abundance and spatial distribution, based on 1 year of monthly samplings from August 2001 to August 2002 and routine coastal monitoring (in late July–early August) between 1994 and 2003. The bay can be divided into three rather distinct parts. The fish fauna of the inner part (salinity 0–2 p.p.t.) is different from two open parts and resembles that of freshwater lakes. In the openmost part (salinity usually 4–6 p.p.t.) some marine species, such as herring Clupea harengus membras, flounder Platichthys flesus and eelpout Zoarces viviparus may seasonally be abundant. Species composition and abundance of most species varies seasonally and interannually. Only the abundance of few species such as pike Esox lucius and pikeperch Stizostedion lucioperca was not impacted by seasonality. The most dynamic period in the bay is spring, when several species (some of them very rare in summer, such as herring and smelt Osmerus eperlanus) enter the bay for spawning.

Dynamics of coastal fish assemblages in the Baltic Sea are still rather poorly understood. In particular, little information is available on migrations and movements of the small‐bodied littoral fish species like Eurasian minnow (Phoxinus phoxinus L.). Minnow is considered typically as a river and lake species, but it also inhabits brackish coastal waters of the Baltic Sea. In this study, we investigated movement patterns of brackish water inhabiting minnows using otolith microchemistry. Fish were collected from four different sites (from two bays and two stream mouths) around Saaremaa Island. The results indicated that at least three distinct migration patterns exist: (i) seawater residency, (ii) fast springtime migrations to fresh water or to bays with lower salinities (areas near stream mouths) and (iii) prolonged migrations to fresh water (some cases overwintering in streams). Migration patterns listed above were not evenly distributed among sites, and some individuals did not migrate to fresh water in every year. None of the analysed fish were freshwater residents. Additionally, potentially ontogenetic effects on Mn and Sr concentrations were observed in the otolith core regions, which may have important implications for the interpretation of otolith chemistry data. The overall findings of this study demonstrate that much more complex migration patterns exists in brackish water inhabiting minnow populations than previously thought and at least some individuals do enter freshwater to reproduce.

– Body length, age, egg size, embryo salinity tolerance and length at hatching of the freshwater (salinity <0.1 ppt, Lake Peipsi) and brackish‐water (salinity 2–6 ppt, Pärnu and Matsalu Bay) ruffe, Gymnocephalus cernuus (L.), were examined to reveal their reproductive success in moderate salinity. Eggs of females originating from brackish water were significantly larger than eggs of freshwater females. No correlation between egg size and female size and age was found in brackish‐water populations. In the freshwater population there was a small negative correlation between egg size and female size, but no correlation with female age. Fertilisation by sperm of males of different origin (brackish water or freshwater) produced no significant differences at any critical developmental stage (fertilisation, gastrulation, hatching) in the development of eggs from brackish‐water or freshwater females at 3.3, 5.5, 7.7 and 9.9 ppt salinity. Survival rates in different salinity depended only on female origin; embryonic salinity tolerance was higher in ruffe inhabiting brackish water. Obviously, embryo salinity tolerance in ruffe is determined by egg qualities.

Age of fish at maturation depends on the species and environmental factors but, in general, investment in growth is prioritized until the first sexual maturity, after which a considerable and increasing proportion of resources are used for reproduction. The present study summarizes for the first the key elements of the maturation of European smelt (Osmerus eperlanus) young of the year (YoY) in the North-eastern Gulf of Riga (the Baltic Sea). Prior to the changes in climatic conditions and collapse of smelt fishery in the 1990s in the Gulf of Riga, smelt attained sexual maturity at the age of 3-4 years. We found a substantial share (22%) of YoY smelt with maturing gonads after the collapse of the smelt fisheries. Maturing individuals had a significantly higher weight, length and condition factor than immature YOY, indicating the importance of individual growth rates in the maturation process. The proportion of maturing YoY individuals increased with fish size. We discuss the factors behind prioritizing reproduction overgrowth in early life and its implications for the smelt population dynamics.