Life history correlates of responses to fisheries exploitation

We use an approach based on phylogenetic comparisons to identify life history correlates of abundance trends in 18 intensively exploited fish stocks from the north-east Atlantic. After accounting for differences in fishing mortality, we show that those fishes that have decreased in abundance compared with their nearest relatives mature later, attain a larger maximum size, and exhibit significantly lower potential rates of population increase. Such trends were not evident in a more traditional cross-species analysis. This is the first phylogenetically independent evidence to link life histories with abundance trends, and provides a quantitative basis for assessing vulnerability of fish populations to exploitation. Our approach can be applied to the conservation and management of other exploited taxa.     

Fishing impacts on the marine inorganic carbon cycle

1.  Teleost fish excrete precipitated carbonate and make significant contributions to the marine inorganic carbon cycle at regional and global scales. As total carbonate production is linked to fish size and abundance, fishing is predicted to affect carbonate production by modifying fish abundance and size-structure.
2.  We draw on concepts from physiology, metabolic ecology, life history theory, population dynamics and community ecology to develop, validate and apply analytical tools to assess fishing impacts on carbonate production. Outputs suggest that population and community carbonate production fall rapidly at lower rates of fishing than those used as management targets for sustainable yield.
3.  Theoretical predictions are corroborated by estimated trends in carbonate production by a herring population and a coral reef fish community subject to fishing. Our analytical results build on widely applicable relationships between life history parameters and metabolic rates, and can be generalized to most fished ecosystems.
4.   Synthesis and applications . If the maintenance of chemical processes as well as biological process were adopted as a management objective for fisheries then the methods we have developed can be applied to assess the effects of fishing on carbonate production and to advise on acceptable rates of fishing. Maintenance of this ecosystem service would require lower rates of fishing mortality than those recommended to achieve sustainable yield.     

Population declines of tuna and relatives depend on their speed of life

Larger-bodied species in a wide range of taxonomic groups including mammals, fishes and birds tend to decline more steeply and are at greater risk of extinction. Yet, the diversity in life histories is governed not only by body size, but also by time-related traits. A key question is whether this size-dependency of vulnerability also holds, not just locally, but globally across a wider range of environments. We test the relative importance of size- and time-related life-history traits and fishing mortality in determining population declines and current exploitation status in tunas and their relatives. We use high-quality datasets of half a century of population trajectories combined with population-level fishing mortalities and life-history traits. Time-related traits (e.g. growth rate), rather than size-related traits (e.g. maximum size), better explain the extent and rate of declines and current exploitation status across tuna assemblages, after controlling for fishing mortality. Consequently, there is strong geographical patterning in population declines, such that populations with slower life histories (found at higher cooler latitudes) have declined most and more steeply and have a higher probability of being overfished than populations with faster life histories (found at tropical latitudes). Hence, the strong, temperature-driven, latitudinal gradients in life-history traits may underlie the global patterning of population declines, fisheries collapses and local extinctions.     

Life-history correlates of maximum population growth rates in marine fishes

Theory predicts that populations of animals with late maturity, low fecundity, large body size and low body growth rates will have low potential rates of population increase at low abundance. If this is true, then these traits may be used to predict the intrinsic rate of increase for species or populations, as well as extinction risks. We used life-history and population data for 63 stocks of commercially exploited fish species from the northeast Atlantic to test relationships between life-history parameters and the rate of population increase at low abundance. We used cross-taxonomic analyses among stocks and among species, and analyses that accounted for phylogenetic relationships. These analyses confirmed that large-bodied, slow-growing stocks and species had significantly lower rates of recruitment and adult production per spawning adult at low abundance. Furthermore, high ages at maturity were significantly correlated with low maximum recruit production. Contrary to expectation, fecundity was significantly negatively related to recruit production, due to its positive relationship with maximum body size. Our results support theoretical predictions, and suggest that a simply measured life-history parameter can provide a useful tool for predicting rates of recovery from low population abundance.     

Body size‐dependent responses of a marine fish assemblage to climate change and fishing over a century‐long scale

Commercial fishing and climate change have influenced the composition of marine fish assemblages worldwide, but we require a better understanding of their relative influence on long‐term changes in species abundance and body‐size distributions. In this study, we investigated long‐term (1911–2007) variability within a demersal fish assemblage in the western English Channel. The region has been subject to commercial fisheries throughout most of the past century, and has undergone interannual changes in sea temperature of over 2.0 °C. We focussed on a core 30 species that comprised 99% of total individuals sampled in the assemblage. Analyses showed that temporal trends in the abundance of smaller multispecies size classes followed thermal regime changes, but that there were persistent declines in abundance of larger size classes. Consistent with these results, larger‐growing individual species had the greatest declines in body size, and the most constant declines in abundance, while abundance changes of smaller‐growing species were more closely linked to preceding sea temperatures. Together these analyses are suggestive of dichotomous size‐dependent responses of species to long‐term climate change and commercial fishing over a century scale. Small species had rapid responses to the prevailing thermal environment, suggesting their life history traits predisposed populations to respond quickly to changing climates. Larger species declined in abundance and size, reflecting expectations from sustained size‐selective overharvesting. These results demonstrate the importance of considering species traits when developing indicators of human and climatic impacts on marine fauna.     

Natural fishing experiments in marine reserves 1983 – 1993: roles of life history and fishing intensity in family responses

 This study examined the effect of fishing on the abundance and species richness of families of coral reef fish at two islands (Sumilon and Apo) in the Philippines from 1983 to 1993. Natural fishing experiments occurred in marine reserves at each island, where long term estimates of fishing intensity were available. Responses to fishing were interpreted in terms of life histories of fish. The intensity of fishing and fish life histories were generally good predictors of the differential rates of decline and recovery of abundance in response to fishing. Large predators had vulnerable life histories (low rates of natural mortality, growth and recruitment) and were subjected to high intensity fishing. They declined significantly in density when fished and increased significantly but slowly when protected from fishing. Caesionidae, a family with a life history resilient to fishing (high rates of natural mortality, growth and recruitment) but fished intensively also declined rapidly in abundance when fished. Thus, knowledge of life history alone was insufficient to predict response to fishing. Acanthuridae were fished relatively hard and had a life history of intermediate vulnerability but displayed weak responses to fishing. Thus level of fishing intensity alone was also not sufficient to predict response to fishing. For Chaetodontidae, effects of fishing conformed to expectations based on life history and fishing intensity at one island but not the other. Three families with intermediate vulnerability and subjected to intermediate to light fishing (F. Scaridae, Labridae and Mullidae) displayed predictably weak responses to fishing, or counter-intuitive responses (e.g., increasing in abundance following fishing). These counter-intuitive responses were unlikely to be secondary effects of increase in prey in response to declines of predators. Two lightly-fished families with resilient life histories (F. Pomacentridae, Sub F. Anthiinae) predictably displayed weak numerical responses to fishing except during a period of use of explosives and drive nets. Accepted: 30 June 1998     

Habitat specialization in tropical continental shelf demersal fish assemblages

The implications of shallow water impacts such as fishing and climate change on fish assemblages are generally considered in isolation from the distribution and abundance of these fish assemblages in adjacent deeper waters. We investigate the abundance and length of demersal fish assemblages across a section of tropical continental shelf at Ningaloo Reef, Western Australia, to identify fish and fish habitat relationships across steep gradients in depth and in different benthic habitat types. The assemblage composition of demersal fish were assessed from baited remote underwater stereo-video samples (n = 304) collected from 16 depth and habitat combinations. Samples were collected across a depth range poorly represented in the literature from the fringing reef lagoon (1-10 m depth), down the fore reef slope to the reef base (10-30 m depth) then across the adjacent continental shelf (30-110 m depth). Multivariate analyses showed that there were distinctive fish assemblages and different sized fish were associated with each habitat/depth category. Species richness, MaxN and diversity declined with depth, while average length and trophic level increased. The assemblage structure, diversity, size and trophic structure of demersal fishes changes from shallow inshore habitats to deeper water habitats. More habitat specialists (unique species per habitat/depth category) were associated with the reef slope and reef base than other habitats, but offshore sponge-dominated habitats and inshore coral-dominated reef also supported unique species. This suggests that marine protected areas in shallow coral-dominated reef habitats may not adequately protect those species whose depth distribution extends beyond shallow habitats, or other significant elements of demersal fish biodiversity. The ontogenetic habitat partitioning which is characteristic of many species, suggests that to maintain entire species life histories it is necessary to protect corridors of connected habitats through which fish can migrate.     

Can life‐history and defence traits predict the population dynamics and natural enemy responses of insect herbivores?

Abstract.  1. Life-history differences between herbivorous insects with eruptive and latent population dynamics are potentially useful for predicting population size variability. An association has also been demonstrated between herbivorous insect defence traits and the responses of various natural enemies.
2. Here predictions of population dynamics and natural enemy responses based on life-history and defence traits are tested using Gonometa postica Walker and G. rufobrunnea Aurivillius, two Southern Hemisphere Macrolepidoptera (Lasiocampidae) species. The temporal and spatial variation in pupal abundance and patterns of pupal parasitism and predation for both species are described and quantified for the first time.
3. Eleven sites were sampled over four generations across the region where both species have historically reached high population densities. Although there was evidence suggesting that population synchrony is driven by weather patterns, site-specific environmental differences contributed to the observed population variability. This study is the first to quantify the extent of population size variability of a species with an intermediate position on the eruptive–latent population dynamic gradient, where data on insect population dynamics is scarce.
4. Support for the life-history–population dynamic relationship was found, as intermediate population size variability for these species was observed. Larval and pupal defence traits, however, were poor and inconsistent predictors of mortality rate. Pupal cocoon structure differences, previously documented for these Gonometa species, may in fact explain the interspecific differences in natural enemy responses found.
5. Predicted population dynamics and natural enemy responses may, however, be overridden by ecological conditions. Nevertheless, life-history and defence traits provide a useful basis for predicting population dynamics of poorly studied species.     

Exploring the dynamics of ecological indicators using food web models fitted to time series of abundance and catch data

Previously, standardized snap-shot models of the Southern Benguela (1980–1989), Southern Humboldt (1992) and Southern Catalan Sea (1994) ecosystems were examined and found to facilitate assessment of ecosystem characteristics related to the gradient in exploitation status of the ecosystems; highest level of exploitation in the South Catalan Sea (North-western Mediterranean), high in the Southern Humboldt and lower in the Southern Benguela. Subsequently, these models were calibrated and fitted using available catch, fishing effort/mortality and abundance data series and incorporated environmental and internal drivers. This study furthers the previous comparative analyses by comparing changes in ecosystem structure using a selection of ecosystem indicators from the calibrated models and assessing how these indicators change over time in these three contrasting ecosystems. Indicators examined include community turnover rates (production/biomass), trophic level of landings and the community, biodiversity indicators, ratios of predatory/forage fish and pelagic/demersal fish biomass, catch ratios, and network analysis indicators. Using the set of model-derived indicators, the three ecosystems were ranked in terms of exploitation level. This ranking was performed using the values of these indicators in recent years (ecosystem state) as well as their trends over time (ecosystem trend). The non-parametric Kruskal–Wallis and Median tests were used to test for significance of the difference between indicators from the three ecosystems in the last 5 years of the simulation to compare present ecosystem states. We compared the slope of the lineal trend and its significance between ecosystems using the generalized least-squares regression taking auto-correlation into consideration to analyse ecosystem trends. The indicators that capture better the high impacts of fishing prevalent in the Mediterranean and Humboldt ecosystems, and the more conservative exploitation of the Southern Benguela, are the fish/invertebrates biomass and catch ratio, the demersal/pelagic fish biomass and catch ratio (depending on the ecosystem and the fishery being developed), flows to detritus, and the mean trophic level of the community (when large, poorly quantified groups such as zooplankton and detritus are excluded). This study suggests that the best option for classifying ecosystems according to the impact of fishing is to consider a broad range of indicators to understand how and why an ecosystem is responding to particular environmental or fishing drivers (or more likely a combination of these). Our results highlight the importance of including indicators capturing trends over time as well as recent ecosystem states. We also identified 23 pairs of indicators that correlated similarly in the three ecosystems (they showed a significant correlation with same sign). Further comparisons may contribute towards generalization of this list, progressing towards a better understanding of the behaviour of ecological indicators.     

Kenyan coral reef lagoon fish: effects of fishing,substrate complexity,and sea urchins

Population density, number of species, diversity, and species-area relationships of fish species in eight common coral reef-associated families were studied in three marine parks receiving total protection from fishing, four sites with unregulated fishing, and one reef which recently received protection from fishing (referred to as a transition reef). Data on coral cover, reef topographic complexity, and sea urchin abundance were collected and correlated with fish abundance and species richness. The most striking result of this survey is a consistent and large reduction in the population density and species richness of 5 families (surgeonfish, triggerfish, butterflyfish, angelfish, and parrotfish). Poor recovery of parrotfish in the transition reef, relative to other fish families, is interpreted as evidence for competitive exclusion of parrotfish by sea urchins. Reef substrate complexity is significantly associated with fish abundance and diversity, but data suggest different responses for protected versus fished reefs, protected reefs having higher species richness and numbers of individuals than unprotected reefs for the same reef complexity. Sea urchin abundance is negatively associated with numbers of fish and fish species but the interrelationship between sea urchins, substrate complexity, coral cover, and management make it difficult to attribute a set percent of variance to each factor-although fishing versus no fishing appears to be the strongest variable in predicting numbers of individuals and species of fish, and their community similarity. Localized species extirpation is evident for many species on fished reefs (for the sampled area of 1.0 ha). Fifty-two of 110 species found on protected reefs were not found on unprotected reefs.     

Evaluation of pulse fishing for the walleye, Stizostedion vitreum vitreum, in Henderson Lake, Ontario

A total of 3226 walleye were removed from Henderson Lake, Ontario over 3 years (1980–2), causing the stock to collapse. This removal tested the applicability of 'pulse' fishing as a management alternative, and also provided an opportunity to determine which population characteristics might be monitored to serve as predictors of stock collapse in this species.
Following initial exploitation, increased length at age occurred only within younger age-lasses. To use this response as a predictor, one must first obtain pre-exploitation length-at-age data through using the proper gear to sample small fish. Abrosov's mean age to mean age at maturity index may also forewarn of stress (1.2 critical t value for Henderson Lake), but poor recruitment usually invalidates this index, since the lower angling vulnerability of large fish biases mean age calculations. While annual production estimates were a good indicator of the collapse, their determination required much effort. Petersen population estimates produced much more realistic estimates of population size than Schumacher–Eschmeyer estimates, but both estimates not only require much effort but also are influenced by changes in recruitment.
Poor predictors of the walleye collapse included: catch-per-unit-effort data, which, while giving some idea of fish density, were not good indices of exploitation stress; condition factors, which were not correlated to fish abundance; fecundity increases, which suffered far too much of a retarded response in Henderson Lake to serve as a predictor of stock collapse. The inability to determine accurately sex ratios of measure recruitment made these parameters unless.
At least over the short term, neither northern pike nor white sucker populations have increased following the walleye collapse. As yet, walleye have not returned to their former abundance, so the operational usefulness of 'pulse' fishing remains an unknown.     

Fish functional diversity as an indicator of resilience to industrial fishing in Patagonia Argentina

The relationship between fish functional diversity and fishing levels at which its baselines shift is important to identify the consequences of fishing in ecosystem functioning. For the first time, the authors of this study implemented a trait-based approach in the Argentine Patagonian Sea to identify the vulnerability and spatiotemporal changes in functional diversity of fish assemblages incidentally captured by a trawling fleet targeting the Argentine red shrimp Pleoticus muelleri (Spence Bate, 1888) between 2003 and 2014. The authors coupled seven fish trophic traits to a reconstructed fish assemblage for the study area and by-catch and evaluated changes in fish species richness and four complementary functional diversity measures (functional richness, redundancy, dispersion and community trait values) along with fishing intensity, temporal use, latitudinal location and depth of fishing grounds, and vessel length. Resident fishes larger than 30 cm in length, with depressed and fusiform bodies, intermediate to high trophic levels, and feeding in benthic, demersal and midwater areas were vulnerable to by-catch. In addition, fish assemblages exhibited a low functional trait redundancy, likely related to species influxes in a biogeographic ecotone with tropicalisation signs. Significant increases in fish trait richness and dispersion poleward and deep suggested new functional roles in these grounds, matching trends in community body size, reproductive load, maximum depth and trophic level. Finally, a temporal increase in fish species and functional trait removal in fishing grounds led to trait homogenisation since 2003. The authors identified that tipping points in temperate fish functional trait diversity showed the importance of trait-based approaches within ecosystem-based fisheries management.     

Thermal affinity as the dominant factor changing Mediterranean fish abundances

Recent decades have seen profound changes in species abundance and community composition. In the marine environment, the major anthropogenic drivers of change comprise exploitation, invasion by nonindigenous species, and climate change. However, the magnitude of these stressors has been widely debated and we lack empirical estimates of their relative importance. In this study, we focused on Eastern Mediterranean, a region exposed to an invasion of species of Red Sea origin, extreme climate change, and high fishing pressure. We estimated changes in fish abundance using two fish trawl surveys spanning a 20‐year period, and correlated these changes with estimated sensitivity of species to the different stressors. We estimated sensitivity to invasion using the trait similarity between indigenous and nonindigenous species; sensitivity to fishing using a published composite index based on the species’ life‐history; and sensitivity to climate change using species climatic affinity based on occurrence data. Using both a meta‐analytical method and random forest analysis, we found that for shallow‐water species the most important driver of population size changes is sensitivity to climate change. Species with an affinity to warm climates increased in relative abundance and species with an affinity to cold climates decreased suggesting a strong response to warming local sea temperatures over recent decades. This decrease in the abundance of cold‐water‐associated species at the trailing “warm” end of their distribution has been rarely documented. Despite the immense biomass of nonindigenous species and the presumed high fishing pressure, these two latter factors seem to have only a minor role in explaining abundance changes. The decline in abundance of indigenous species of cold‐water origin indicates a future major restructuring of fish communities in the Mediterranean in response to the ongoing warming, with unknown impacts on ecosystem function.     

Measuring marine fishes biodiversity: temporal changes in abundance, life history and demography

Patterns in marine fishes biodiversity can be assessed by quantifying temporal variation in rate of population change, abundance, life history and demography concomitant with long-term reductions in abundance. Based on data for 178 populations (62 species) from four north-temperate oceanic regions (Northeast Atlantic and Pacific, Northwest Atlantic, North mid-Atlantic), 81% of the populations in decline prior to 1992 experienced reductions in their rate of loss thereafter; species whose rate of population decline accelerated after 1992 were predominantly top predators such as Atlantic cod (Gadus morhua), sole (Solea solea) and pelagic sharks. Combining population data across regions and species, marine fishes have declined 35% since 1978 and are currently less than 70% of recorded maxima; demersal species are generally at historic lows, pelagic species are generally stable or increasing in abundance. Declines by demersal species have been associated with substantive increases in pelagic species, a pattern consistent with the hypothesis that increases in the latter may be largely attributable to reduced predation mortality. There is a need to determine the consequences to population growth effected by the reductions in age and size at maturity, and in mean age and size of spawners, concomitant with population decline. We conclude that reductions in the rate of population decline, in the absence of targets for population increase, will be insufficient to effect a recovery of marine fishes biodiversity, and that great care must be exercised when interpreting multi-species patterns in abundance. Of fundamental importance is the need to explain the geographical, species-specific and habitat biases that pervade patterns of marine fishes recovery and biodiversity.     

Effects of fishing on parasitism in a sparid fish: contrasts between two areas of the Western Mediterranean

This study addressed the impacts of fishing on the rates of parasitism using the sparid Boops boops as a model fish species. Using a large suite of parasite species in B. boops, with different life histories, transmission pathways and host specificity, we compared parasite diversity, prevalence, abundance and community structure at two Mediterranean localities in the Balearic Sea, Santa Pola Bay and the Gulf of Oran, that are characterised by a contrasting pattern of fishing of B. boops. A total of 360 fish were examined comprising nine distinct samples collected during the warm and the cold weather months. A total of 29 parasite species were identified, with eight species in common for the two localities. Parasite component communities at Santa Pola Bay were more species rich and abundant than those at the Gulf of Oran and exhibited a different community structure. Of the eight common taxa used in the quantitative comparisons, five exhibited significant difference for prevalence between the two localities, four having substantially higher prevalence at Santa Pola and only one being more prevalent at the Gulf of Oran. Two specialist trematodes and the sparid generalist monogenean exhibited consistently higher prevalence and abundance at Santa Pola Bay than at the Gulf of Oran; the two specialists were also identified as key species for assigning individual fish to their locality of origin. The consistent differences in the richness, abundance and structure of parasite communities in B. boops from Santa Pola Bay and the Gulf of Oran may reflect the contrasting patterns of exploitation of the populations of this fish host at the two localities.     

Spatial and temporal variation in a suite of life-history traits in two species of wolf spider

Abstract.  1. Life-history traits and density were assayed in seven populations of two sympatric species of wolf spider for three consecutive years. The goal of the study was to quantify population dynamics and its relation to spatial and temporal life-history variation.
2. Adult female body size and fecundity varied significantly, among field sites and among years, in both species. Female spiders of both species differed in mean relative reproductive effort among sites, but not among years. The size of offspring was invariable, with no significant differences due to site or year.
3. All populations of both species tended to either decrease or increase in density during a given year and this was tightly correlated with changes in prey consumption rates.
4. Since life-history patterns are determined primarily by selection, it is concluded that size at sexual maturity for females is phenotypically plastic and responds to changes in prey availability. Offspring size however is not plastic and it is likely that other selection forces have determined offspring size. Temporal fluctuations in population size are correlated over a large area relative to dispersal capabilities for these species and conservation efforts for invertebrates must take this into consideration.     

Life history variation in Barents Sea fish: implications for sensitivity to fishing in a changing environment

• Under exploitation and environmental change, it is essential to assess the sensitivity and vulnerability of marine ecosystems to such stress. A species' response to stress depends on its life history. Sensitivity to harvesting is related to the life history “fast–slow” continuum, where “slow” species (i.e., large, long lived, and late maturing) are expected to be more sensitive to fishing than “fast” ones. We analyze life history traits variation for all common fish species in the Barents Sea and rank fishes along fast–slow gradients obtained by ordination analyses. In addition, we integrate species' fast–slow ranks with ecosystem survey data for the period 2004–2009, to assess life history variation at the community level in space and time. Arctic fishes were smaller, had shorter life spans, earlier maturation, larger offspring, and lower fecundity than boreal ones. Arctic fishes could thus be considered faster than the boreal species, even when body size was corrected for. Phylogenetically related species possessed similar life histories. Early in the study period, we found a strong spatial gradient, where members of fish assemblages in the southwestern Barents Sea displayed slower life histories than in the northeast. However, in later, warmer years, the gradient weakened caused by a northward movement of boreal species. As a consequence, the northeast experienced increasing proportions of slower fish species. This study is a step toward integrating life history traits in ecosystem‐based areal management. On the basis of life history traits, we assess the fish sensitivity to fishing, at the species and community level. We show that climate warming promotes a borealization of fish assemblages in the northeast, associated with slower life histories in that area. The biology of Arctic species is still poorly known, and boreal species that now establish in the Arctic are fishery sensitive, which calls for cautious ecosystem management of these areas.

     

Age,growth, mortality and population structure of silver croaker Pennahia argentata (Houttuyn, 1782) and red bigeye Priacanthus macracanthus Cuvier, 1829 in the north‐central Taiwan Strait

The main objectives of this study were to estimate the age, growth, mortality and population structure of silver croaker Pennahia argentata (Houttuyn, 1782) and red bigeye Priacanthus macracanthus Cuvier, 1829 and to explore the factors causing the fluctuation of the fish populations and the ecological parameters. The two species were randomly sampled, with 80~120 individuals of each species captured every month from a single trawler fishery (mesh size 250 mm), March to November 2006, in the north‐central Taiwan Strait. A total of 994 speciments of silver croaker and 851 speciments of red bigeye were collected. Compared with previous studies, the mean length and weight, mean age, the minimum size at first sexual maturity, the asymptotic length (L_∞) and weight (W_∞) of the two species has decreased in recent decades, indicating that the populations were younger, smaller and earlier in sexual maturity. Meanwhile, the growth coefficient (K) increased, the mortality coefficients (Z, F, M) were higher, and the exploitation rate (E) indicated overfishing. Fishing is a key driving force that can cause abundant fluctuations and changes in ecological characteristics in these two demersal fishes in this area. Accordingly, the traditional fishery management approach, such as the reduction in fishing effort, coupled with the Ecosystem‐based Fishery Management (EBFM) should be implemented to achieve sustainable demersal fisheries.     

Contrasting life-history traits of two sympatric smooth-hound species: implication for vulnerability

In this study, life-history traits (maximum and average size, size at maturity and fecundity) of two congeneric smooth-hounds, Mustelus mustelus and Mustelus punctulatus, which share a geographical distribution and experience a similar fishing exploitation, were estimated and compared between species. The results indicated a lower maximum and average size, a lower size at maturity and a higher fecundity in M. punctulatus compared with those in M. mustelus. Considering that these two species co-occur in the same areas and are caught by the same fishing gears, the results indicate a higher vulnerability to exploitation of M. mustelus compared with that of M. punctulatus.     

Ichthyofaunal assemblages in estuaries: A South African case study

This review places the life-history styles of fishes associated with South African estuaries in a global context and presents a classification system incorporating all the major life-history categories for estuary-associated fish species around the world. In addition, it documents the early life histories of the major fish groups in South African estuaries, with particular emphasis on the differing modes of estuarine utilization by marine, estuarine and freshwater taxa.This review details factors influencing the ichthyofaunal community structure in South African estuaries. The availability of fish for recruitment into an estuary depends primarily upon the distributional range of euryhaline marine and estuarine species, with tropical and temperate taxa showing marked abundance trends. Within a particular biogeographic region, however, estuarine type and prevailing salinity regime have a major influence on the detailed ichthyofaunal structure that develops. There is an increasing preponderance of marine fish taxa when moving from a freshwater-dominated towards a seawater-dominated type of system, and a decline in species diversity between subtropical estuaries in the north-east and cool temperate systems in the south-west. Similar declines in fish species diversity between tropical and temperate estuaries in other parts of the world are highlighted.Fish assemblages in estuaries adjust constantly in response to changing seasons, salinities, turbidities, etc. Despite persistent fluctuations in both the biotic and abiotic environment, the basic ichthyofaunal structure appears to have an underlying stability and to be predictable in terms of the response of individual species to specific conditions. This stability seems to be governed by factors such as the dominance of eurytopic taxa within estuarine assemblages and the robust nature of food webs within these systems. The predictability arises from factors such as the seasonality associated with estuarine spawning cycles and juvenile fish recruitment patterns. These patterns, together with a well-documented resilience to a wide range of physico-chemical and biotic perturbations, appear to be an underlying feature of fish assemblages in estuaries around the world.In contrast to marine fish species, estuary-associated taxa have received little conservation attention. Apart from the designation of protected areas, the main direct means of conserving estuary-associated fish stocks include habitat conservation and controls over fishing methods, effort, efficiency and seasonality. Of these, the conservation of fish habitats, the most important, because healthy aquatic environments invariably support healthy fish populations. The use of estuarine sanctuaries for fish conservation is briefly reviewed, as well as the legislation governing the USA National Estuarine Research Reserve System (NERRS) and the Australian Marine and Estuarine Protected Area (MEPA) system. It is concluded that South Africa requires an expansion of the existing Estuarine Protected Area (EPA) network, as well as the upgrading of selected 'estuarine reserves' where fishing is permitted, into 'estuarine sanctuaries' where no exploitation of biological resources is allowed.