Age‐ or length‐structured stock assessments require reliable life history demographic parameters (growth, mortality, reproduction) to model population dynamics, potential yields and stock sustainability. This study synthesized life history information for 84 commercially exploited tropical reef fish species from Florida and the U.S. Caribbean (Puerto Rico and the U.S. Virgin Islands). We attempted to identify a useable set of life history parameters for each species that included lifespan, length at age, weight at length and maturity at length. Key aspects of the life history synthesis were development of: (a) a database that characterized study details including sampling region, biological and statistical methods, length range of sampled individuals, sample size, capture gears and sampling time frame; (b) reproducible procedural criteria for parameter identification for a given species; and (c) a reliability metric for each parameter type. Complete life history parameter sets were available for 46 species analysed. Of these, only 16 species had parameter sets meeting the highest standards for reliability, highlighting future research needs. 相似文献
Effects of training at a regular, fixed, standard exercise load on venous lactic acid, mixed venous and arterial blood gases and pH, and serum muscle enzymes were determined on previously unconditioned, healthy, adult, Standardbred horses. Arterial and mixed venous blood gases, pH, and serum muscle enzymes did not change in a consistent manner during training. Venous lactic acid concentrations did increase significantly with training and may be of value for the biochemical evaluation of fitness in horses. 相似文献
A kinesis model driven by high-resolution sea surface temperature maps is used to simulate Atlantic bluefin tuna movements in the Gulf of Maine during summer months. Simulations showed that individuals concentrated in areas of thermal preference. Results are compared to empirical distribution maps of bluefin tuna schools determined from aerial overflights of the stock during the same time periods. Simulations and empirical observations showed similar bluefin tuna distributions along fronts, although interannual variations in temperature ranges occupied suggest that additional foraging factors are involved. Performance of the model is further tested by simulating the relatively large-scale annual north–south migrations of bluefin tuna that followed a preferred thermal regime. Despite the model's relatively simple structure, results suggest that kinesis is an effective mechanism for describing movements of large pelagic fish in the expansive ocean environment. 相似文献
We examine the influence of reserve size and boundary length on the relative rate of fish density change in reserves versus fished reference reefs for three exploitable-sized reef fish categories: (1) combined fish (34 species of Haemulidae, Lutjanidae, Serranidae, and hogfish Lachnolaimus maximus); (2) Haemulidae (13 species); and (3) Lutjanidae (9 species). If reef habitat boundaries are highly permeable to fish movements then fish recovery within a reserve would be inversely proportional to: reserve perimeter (RP)/total reserve area (RA) (RP/RA). If, however, reef habitat boundaries are relatively impermeable barriers to fish movements, recovery within the reserve would be inversely proportional to: reserve boundary that intersects reef habitat (HI)/reef habitat area within the reserve (HA) (HI/HA). From 1994 to 2001 we monitored reef fishes within and outside of no-take marine reserves established in 1997 in the Florida Keys, USA. A significant majority of reserves had greater rates of density change than reference reefs for Lutjanidae and combined fish (22 of 24 reserves for both categories). Significantly higher rates of density change were found in ten reserves for Lutjanidae, two reserves for combined fish, and one reserve for Haemulidae. Reserves appeared to promote an increased density of exploitable fishes. A significant, negative, but weakly correlated relationship was found between the relative rate of density change (RDC) for combined fish and the HI/HA ratio. Reserve size and placement appeared to have a minimal effect upon RDC.