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1.
Book review     
The Cost of Environmental Protection: Regulating Housing in the Coastal Zone by Dan K. Richardson. Published by the Center for Urban Policy Research Rutgers University, 1976. 250 pp., $10.00.  相似文献   

2.
Book review     
Coastal Resource Use: Decisions on Puget Sound by Robert L. Bish, Robert Warren, Louis F. Weschler, James A. Crutchfield, and Peter Harrison.

Published by University of Washington Press in cooperation with Washington Sea Grant Program, 1975. 206 pp., 15 figs.  相似文献   

3.
Book reviews     
R. S. Farrow, with J. M. Broadus, T. A. Grigalunas, P. Hoagland III, and J. J. Opaluch. 1990. Managing the Outer Continental Shelf Lands: Oceans of Controversy. New York: Taylor & Francis New York, 168 pp., paper.

Richard A. Kenchington. 1990. Managing Marine Environments. New York: Taylor & Francis, 248 pp.  相似文献   

4.
Book review     
Recreation: Marine Promise, Proceedings of the National Conference on Marine Recreation Susan H. Andersen, Ed., October 2–4, 1975, Newport Beach, California

Parable Beach: A Primer in Coastal Zone Economics by J. W. Devanney III, G. Ashe, and B. Parkhurst, The MIT Press, 1976, 99 pp.

Marine Recreational Fisheries, Proceedings of the First Annual Marine Recreational Fisheries Symposium Henry Clepper, ed., New Orleans, Louisiana, February 27, 1976.  相似文献   

5.
Book review     
Coastal Management: Readings and Notes. Edited by Marc J. Hershman and James H. Feldmann. Institute for Marine Studies, Coastal Resources Program, University of Washington, Seattle (January 1979), 806 pp. $22.50 (paper bound).

Tobey L. Winters, Deepwater Ports in the United States: An Economic and Environmental Impact Study. N.Y. Praeger, 1977, 201 pages.  相似文献   

6.
During 2004, 10 samplings were performed in order to measure dissolved methane (CH4), carbon dioxide (CO2) and nitrous oxide (N2O) in the surface waters of Río San Pedro, a tidal creek in the salt marsh area of the Bay of Cádiz (SW Spain). The inner partvs of the creek is affected by the inputs coming from an intensive fish farm and the drainage of an extensive salt marsh area.Dissolved CH4, CO2 and N2O concentrations ranged from 11 to 88 nM, 36 to 108 μM and 14 to 50 nM, respectively. Surface waters were in all cases oversaturated with respect to the atmosphere, reaching values of up to 5000% for CH4, 1240% for CO2 and 840% for N2O. Dissolved CH4, CO2 and N2O showed a significant tidal and seasonal variability. Over a tidal cycle, concentrations were always highest during low tide, which points to the influence of the inputs from the fish farm effluent and the drainage of the adjacent salt marsh area, as well as in situ production within the system. Dissolved CH4, CO2 and N2O seasonal patterns were similar and showed maximum concentrations in summer conditions. Using four different parameterizations to calculate the gas transfer coefficients [Liss, P.S. and Merlivat, L., 1986. Air-sea exchange rates: introduction and synthesis. In P. Buat-Ménard (Ed.), The Role of Air-Sea Exchanges in Geochemical Cycling. Reidel, Dordrecht, The Netherlands, p. 113–127.; Clark, J.F., Schlosser, P., Simpson, H.J., Stute, M., Wanninkhof, R., and Ho, D.T., 1995. Relationship between gas transfer velocities and wind speeds in the tidal Hudson River determined by the dual tracer technique. In: B. Jähne and E. Monahan (Eds.), Air-Water Gas Transfer: AEON Verlag and Studio, Hanau, Germany, pp. 785–800.; Carini, S., Weston, N., Hopkinson, G., Tucker, J., Giblin, A. and Vallino, J., 1996. Gas exchanges rates in the Parker River estuary, Massachusetts. Biol. Bull., 191: 333–334.; Kremer, J.N., Reischauer, A. and D'Avanzo, C., 2003. Estuary-specific variation in the air-water gas exchange coefficient for oxygen. Estuaries, 26: 829–836.], the averaged air–water fluxes of CH4, CO2 and N2O from the creek to the atmosphere ranged between 34 and 150 μmol CH4 m− 2 day− 1, 73 and 177 mmol CO2 m− 2 day− 1 and 24 and 62 μmol N2O m−2 day−1, respectively.  相似文献   

7.
Estimation of global and regional air–sea fluxes of climatically important gases is a key goal of current climate research programs. Gas transfer velocities needed to compute these fluxes can be estimated by combining altimeter-derived mean square slope with an empirical relation between transfer velocity and mean square slope derived from field measurements of gas fluxes and small-scale wave spectra [Frew, N.M., Bock, E.J., Schimpf, U., Hara, T., Hauβecker, H., Edson, J.B., McGillis, W.R., Nelson, R.K., McKenna, S.P., Uz, B.M., Jähne, B., 2004. Air–sea gas transfer: Its dependence on wind stress, small-scale roughness and surface films, J. Geophys. Res., 109, C08S17, doi: 10.1029/2003JC002131.]. We previously reported initial results from a dual-frequency (Ku- and C-band) altimeter algorithm [Glover, D.M., Frew, N.M., McCue, S.J., Bock, E.J., 2002. A Multi-year Time Series of Global Gas Transfer Velocity from the TOPEX Dual Frequency, Normalized Radar Backscatter Algorithm, In: Gas Transfer at Water Surfaces, editors: Donelan, M., Drennan, W., Saltzman, E., and Wanninkhof, R., Geophysical Monograph 127, American Geophysical Union, Washington, DC, 325–331.] for estimating the air–sea gas transfer velocity (k) from the mean square slope of short wind waves (40–100 rad/m) and derived a 6-year time series of global transfer velocities based on TOPEX observations. Since the launch of the follow-on altimeter Jason-1 in December 2001 and commencement of the TOPEX/Jason-1 Tandem Mission, we have extended this time series to 12 years, with improvements to the model parameters used in our algorithm and using the latest corrected data releases. The prospect of deriving multi-year and interdecadal time series of gas transfer velocity from TOPEX, Jason-1 and follow-on altimeter missions depends on precise intercalibration of the normalized backscatter. During the Tandem Mission collinear phase, both satellites followed identical orbits with a mere 73-s time separation. The resulting collocated, near-coincident normalized radar backscatter (σ°) data from both altimeters present a unique opportunity to intercalibrate the two instruments, compare derived fields of transfer velocity and estimate the precision of the algorithm. Initial results suggest that the monthly gas transfer velocity fields generated from the two altimeters are very similar. Comparison of along-track Ku-band and C-band σ° during the collinear phase indicates that observed discrepancies are due primarily to small offsets between TOPEX and Jason-1 σ°. The Jason-1 k values have an apparent bias of + 4% relative to TOPEX, while the precision estimated from the two observation sets is 5–7% and scales with k. The resultant long-term, global, mean k is 16 cm/h.  相似文献   

8.
Book review     
Onshore Planning for Offshore Oil—Lessons from Scotland by Pamela L. Baldwin and Malcolm F. Baldwin The Conservation Foundation, Washington, D.C., 1975  相似文献   

9.
Individual based numerical simulations of the copepod, Oithona davisae, feeding on motile prey, Oxyrrhis marina, under variable turbulent conditions are performed. These simulations correspond to laboratory observations conducted by Saiz et al. [Saiz, E., Calbet, A., and Broglio, E., 2003. Effects of small-scale turbulence on copepods: the case of Oithona Davisae. Limnol. Oceanogr., 48:1304–1311.].The flow field in the simulation is reconstructed by a kinematic simulation whose characteristic scales are derived from the grid mesh and the dissipation rates of the laboratory experiments. The kinematic simulation provides a simplified model, which while not fully realistic, captures the basic relevant feature of turbulence. A hop and sink swimming behaviour is prescribed for O. davisae, while O. marina moves along helical paths with random changes of directions.Three possible effects are tested: the existence of a time threshold in the duration of the contacts between predator and prey, a progressive reduction of the perceptive distance with increasing turbulence level and an abrupt reduction in feeding of O. davisae when the flow speed, in relation to the copepod position, is higher than a prescribed threshold. This last approach introduces an intermittency in the feeding which depends on the variations of velocity both in space and time within the numerical box.The introduction of the time threshold causes a dome-shaped relationship between the simulated enhancement factor and the dissipation rate, while with the other two effects, a monotonic decrease in the enhancement factor is observed, with values reasonably close to the ones observed in the laboratory experiment. In all the cases, the use of realistic values of biological parameters (e.g. swimming behaviour) reproduces response curves in the range of the observations.  相似文献   

10.
One of the dominant sources of uncertainty in the calculation of air–sea flux of carbon dioxide on a global scale originates from the various parameterizations of the gas transfer velocity, k, that are in use. Whilst it is undisputed that most of these parameterizations have shortcomings and neglect processes which influence air–sea gas exchange and do not scale with wind speed alone, there is no general agreement about their relative accuracy.The most widely used parameterizations are based on non-linear functions of wind speed and, to a lesser extent, on sea surface temperature and salinity. Processes such as surface film damping and whitecapping are known to have an effect on air–sea exchange. More recently published parameterizations use friction velocity, sea surface roughness, and significant wave height. These new parameters can account to some extent for processes such as film damping and whitecapping and could potentially explain the spread of wind-speed based transfer velocities published in the literature.We combine some of the principles of two recently published k parameterizations [Glover, D.M., Frew, N.M., McCue, S.J. and Bock, E.J., 2002. A multiyear time series of global gas transfer velocity from the TOPEX dual frequency, normalized radar backscatter algorithm. In: Donelan, M.A., Drennan, W.M., Saltzman, E.S., and Wanninkhof, R. (Eds.), Gas Transfer at Water Surfaces, Geophys. Monograph 127. AGU,Washington, DC, 325–331; Woolf, D.K., 2005. Parameterization of gas transfer velocities and sea-state dependent wave breaking. Tellus, 57B: 87–94] to calculate k as the sum of a linear function of total mean square slope of the sea surface and a wave breaking parameter. This separates contributions from direct and bubble-mediated gas transfer as suggested by Woolf [Woolf, D.K., 2005. Parameterization of gas transfer velocities and sea-state dependent wave breaking. Tellus, 57B: 87–94] and allows us to quantify contributions from these two processes independently.We then apply our parameterization to a monthly TOPEX altimeter gridded 1.5° × 1.5° data set and compare our results to transfer velocities calculated using the popular wind-based k parameterizations by Wanninkhof [Wanninkhof, R., 1992. Relationship between wind speed and gas exchange over the ocean. J. Geophys. Res., 97: 7373–7382.] and Wanninkhof and McGillis [Wanninkhof, R. and McGillis, W., 1999. A cubic relationship between air−sea CO2 exchange and wind speed. Geophys. Res. Lett., 26(13): 1889–1892]. We show that despite good agreement of the globally averaged transfer velocities, global and regional fluxes differ by up to 100%. These discrepancies are a result of different spatio-temporal distributions of the processes involved in the parameterizations of k, indicating the importance of wave field parameters and a need for further validation.  相似文献   

11.
Sampling of the near-bottom calanoid copepods was performed on board of the research vessel Polarstern in 1993 in the Laptev Sea (Siberian Arctic). Three new species of Xanthocalanus were identified as such, and are described and figured here: X. spinodenticulatus sp. nov., X. laptevorum sp. nov. and X. polarsternae sp. nov.  相似文献   

12.
Stable isotope (δ13C and δ15N) analyses were performed on suprabenthic fauna collected in the western Mediterranean (NW Balearic Islands), at depths ranging between 350 and 780 m. Samples were collected seasonally at bi-monthly intervals during six cruises performed between August 2003 and June 2004, using a Macer-GIROQ suprabenthic sledge (0.5 mm mesh size). Twenty-four separate species (5 mysids, 12 amphipods, 2 cumaceans, 2 isopods, 1 euphausiid, 1 decapod and 1 fish) and bulk copepods were analyzed on a seasonal basis for stable carbon and nitrogen isotopes. Stable nitrogen isotope ratios (δ15N) ranged from 2.3‰ (the amphipod Lepechinella manco in September 2003) to 13.0‰ (the amphipod Rhachotropis caeca in August 2003). δ13C values ranged from − 24.2 (the cumacean Campylaspis sulcata in June 2004) to − 16.1 (the amphipod Bruzelia typica in November 2006). Both δ13C and δ15N values suggest that there are three trophic levels within the suprabenthic community. However, considering the bathymetric range of the species, the results suggest that the deepest assemblage supported only two trophic levels. The stable isotope ratios of suprabenthic fauna displayed a continuum of values and confirmed a wide spectrum of feeding types (from filter-feeders to predators). In general, and in spite of the poor knowledge about diets available for most suprabenthic species, higher δ15N were found for carnivorous amphipods (e.g. Rhachotropis spp., Nicippe tumida) consuming copepods. Low overlap for δ13C and δ15N values was observed, though δ15N values where less variable than δ13C, which suggests high resource partitioning in this assemblage. Seasonal variations in isotopic composition for both δ13C and δ15N were low (less than 1‰ and 3‰, respectively) and variable depending on species. Low correlations between δ13C and δ15N of suprabenthic fauna were found for all periods studied, though increasing from February 2004 to June 2004 (after the main peak of primary production in surface). C:N ratio (indicator of lipid content) showed higher values in summer than in winter. This suggests that lipid content may explain the seasonal patterns of δ13C variability and, due to the increase of storage products in phytoplankton and zooplankton, it possibly indicates the peak of primary production at the surface.  相似文献   

13.
We present concurrent data on ingestion, egg production and the loss of maternal biomass in pre-spring bloom female Calanus finmarchicus incubated under conditions representative of those in situ in the North Atlantic. A balanced metabolic budget was constructed and used to examine the relative importance of ingestion and biomass for fuelling egg production during the incubations. Ingested carbon was not sufficient to meet the observed demands for egg production. More than 80% of the carbon utilised by the females was instead derived from their biomass. Fatty acid analysis demonstrated that the storage reserves, 20:1 (n−9) and 22:1 (n−11), were virtually absent before experimentation began, and therefore could not have been used to supply the carbon required for egg production during the incubations. The C:N mass-specific ratio of the biomass utilised was 4.1, suggesting that the females had instead catabolised protein in order to meet their metabolic demands. These results suggest that C. finmarchicus adopts a sacrificial reproductive strategy when food availability is low.  相似文献   

14.
Three aspects of the appendicularian O. dioica's ecophysiology were measured here: 1) morphological parameters over a wide range of appendicularian sizes, including mature animals in order to document the morphological characteristics inducing reproduction; 2) clearance rate and assimilation efficiency using feeding incubations with different algal concentrations and 3) the effect of food concentration on growth, mortality and reproduction.The relationship between the body carbon weight and the clearance rate follows a power function, with an exponent of 0.91 (± 0.07). The rate of particles retention increases with the food concentration following a Michaelis–Menten relationship (half-saturation constant = 151 ± 22 µg C l− 1, maximum clearance rate = 12 ± 1 µg C µg C− 1 d− 1). The carbon assimilation efficiency decreases with the increasing food concentration. As a result, appendicularian growth which is limited in concentrations lower than 50 µg C l− 1 is saturated above 100 µg C l− 1.In immature animals the gonad represents less than 30% of the body volume whereas in mature individuals, its volume varies between 50% and 87% (mean 63%) suggesting that gonad/total volume ratio can be used as indicator of the maturation stages. The gonad weight in mature animals represents 70.3 (± 4.6)% of the total body carbon weight. Two major maturity stages can explain the changes in energy allocation: i) the somatic growth, when less energy is invested in gonad growth when compared to the rest of the body and ii) the maturation phase where most of the assimilated matter is invested in gonad maturation. This process is rapid, lasting only few hours. For this reason we measured completely mature organisms that are generally not measured during the experimental work with appendicularians. In food-limited conditions, the gonad maturation process starts with smaller individuals and ends with smaller reproductive animals having the same gonad to total volume ratio than in unlimited food conditions. The results obtained in this study were used to model the life cycle of O. dioica (see Lombard, F., Sciandra, A. and Gorsky, G., 2009-this volume. Appendicularian ecophysiology. II. Modeling nutrition, metabolism, growth and reproduction of the appendicularian Oikopleura dioica.).  相似文献   

15.
The egg production of marine copepods correlates with a range of variables, including the availability of organic carbon (C), nitrogen (N) and the polyunsaturated fatty acids (PUFAs) 20:5(n−3) (EPA) and 22:6(n−3) (DHA). However, an understanding of which substrates limit egg production in the natural environment has yet to be reached. The quantities of C, N, EPA and DHA ingested, derived from parental biomass, and invested in eggs by female Calanus finmarchicus during a 5-day incubation experiment were examined using stoichiometric theory to determine which substrate was limiting. The majority of each substrate was derived from parental biomass, and therefore the existing stoichiometric theory is developed to include this route of supply. The females were essentially devoid of lipid reserves, as evidenced by the lack of the storage fatty acids 20:1(n−9) and 22:1(n−11), and carbon limitation was predicted under most of the scenarios examined. Nitrogen limitation was only apparent when carbon and nitrogen utilisation efficiencies were assumed to be high (0.5) and low (0.4) respectively. PUFAs were assumed to be utilised with high efficiency (0.9), and were never predicted to limit production. This work highlights the need for a more detailed understanding of the maintenance requirements that marine copepods have for C, N, EPA, and DHA and hence the efficiencies with these substrates can be utilised for growth.  相似文献   

16.
100-years-changes in the phytoplankton community of Kiel Bight (Baltic Sea)   总被引:1,自引:0,他引:1  
Literature data from 1905/06, 1912/13 and 1949/50 were compared with recent data (2001–2003) from Kiel Bight in order to investigate changes in phytoplankton composition and biomass, which may serve as indicators of environmental changes. In terms of biomass, diatomophyceae and dinophyceae are by far the most important groups. Their ratio is still close to unity. The share of diatomophyceae increased strongly in years with exceptionally high summer blooms (2001) or exceptionally early spring blooms (2003). The summer and autumn blooms of Chaetoceros and Skeletonema, detected in the early 20th century, are replaced by other diatoms (Cerataulina pelagica, Dactyliosolen fragilissimus, Proboscia alata, Pseudo-nitzschia spp.). Chaetoceros and Skeletonema are still important components of the spring blooms. Now as before, the autumn blooms are dominated by Ceratium spp., sometimes also by diatoms. Newly appearing bloom-forming species are mostly potentially toxic (Dictyocha speculum, Prorocentrum minimum, Pseudo-nitzschia spp.). The total phytoplankton biomass has roughly doubled in the course of the last century. The reference condition for phytoplankton biomass in Kiel Bight in the sense of the Water Framework Directive was defined at 55 mg C m− 3 (± 10%, annual mean). The mean annual biomass of diatomophyceae and dinophyceae was 25 mg C m− 3 (± 40%) for each, indicating that the sum of their carbon biomass amounted to 90% (± 10%) of the total phytoplankton biomass on an annual average. Diatomophyceae represented at least 80% of carbon biomass in the spring bloom peak at the beginning of the 20th century.  相似文献   

17.
Estimating salinity to complement observed temperature: 1. Gulf of Mexico   总被引:1,自引:1,他引:0  
This paper and its companion [Thacker, W.C., Sindlinger, L., 2007-this issue. Estimating salinity to complement observed temperature: 2. Northwestern Atlantic. Journal of Marine Systems. doi:10.1016/j.jmarsys.2005.06.007.] document initial efforts in a project with the goal of developing capability for estimating salinity on a region-by-region basis for the world oceans. The primary motivation for this project is to provide information for correcting salinity, and thus density, when assimilating expendable-bathythermograph (XBT) data into numerical simulations of oceanic circulation, while a secondary motivation is to provide information for calibrating salinity from autonomous profiling floats. Empirical relationships between salinity and temperature, which can be identified from archived conductivity–temperature–depth (CTD) data, provide the basis for the salinity estimates.The Gulf of Mexico was chosen as the first region to explore for several reasons: (1) It's geographical separation from the Caribbean Sea and the North Atlantic Ocean makes it a “small ocean” characterised by a deep central basin surrounded by a substantial continental shelf. (2) The archives contain a relatively large number of CTD data that can be used to establish empirical relationships. (3) The sharp fronts associated with the Loop Current and its rings, which separate water with different thermal and haline characteristics, pose a challenge for estimating salinity. In spite of the shelf and the fronts, the relationship between salinity and temperature was found to be sufficiently regular that a single empirical model could be used to estimate salinity on each pressure surface for the entire Gulf for all seasons. In and below the thermocline, root-mean-square estimation errors are small — less than 0.02 psu for pressures greater than 400 dbar, corresponding to potential density errors of less than 0.015 kg/m3. Errors for estimates nearer to the surface can be an order of magnitude larger.  相似文献   

18.
Twelve epipelagic copepod species were reviewed to compare their adaptations to the short primary production season and low temperatures which characterise the Southern Ocean. The species show a spectrum of adaptations, but three broad life cycle strategies were defined: (1) herbivorous in summer, a short reproductive period and winter diapause at depth (Calanoides acutus and possibly Ctenocalanus citer); (2) predominantly omnivorous/detritivorous diet, an extended period of feeding, growth and reproduction and less reliance on diapause at depth (Metridia gerlachei, Calanus propinquus, Calanus simillimus, Oithona similis, Microcalanus pygmaeus, and possibly Oncaea curvata and Oithona frigida); (3) overwintering and feeding within sea ice as early nauplii or copepodids (Stephos longipes and Paralabidocera antarctica). The large species Rhincalanus gigas appears to be intermediate between strategies (1) and (2). Contrasting species from groups (1) and (2), namely C. acutus and O. similis, were selected for more detailed comparison. For C. acutus, maximum (probably food saturated) feeding and egg production rates are well below equivalent values for Calanus spp. at lower latitudes. Likewise, summer growth and moulting rates are slower, and the growth season of this herbivore is only 2–4 months. Therefore, both the low summer temperatures and short primary production season seem to dictate a long (1 year) life cycle for C. acutus. A collation of data on O. similis revealed that its abundance increases about tenfold from the Antarctic shelf northwards to the Polar Frontal Zone, where abundances are similar to those in temperate and tropical shelf seas. In contrast to C. acutus, O. similis appears to remain in the epipelagic and reproduce there year-round, although the food sources which sustain this are still uncertain.  相似文献   

19.
A Lagrangian model is used to simulate and quantify in the northern Humboldt upwelling ecosystem the processes of enrichment, concentration and retention, identified by Bakun [Bakun, A., 1996. Patterns in the ocean. Ocean processes and marine population dynamics. University of California Sea Grant, California, USA, in cooperation with Centro de Investigaciones Biologicas de Noroeste, La Paz, Baja California Sur, Mexico, 323 pp.] as being important for the survival and recruitment of early life stages of pelagic fish. The method relies on tracking the positions of particles within water velocity fields generated by a three-dimensional hydrodynamic model. Simple criteria for considering particles as participating to enrichment, concentration or retention are used to derive indices of the three processes. We analyse the spatial distribution of and seasonal variability in these indices. The results are discussed in relation to anchovy (Engraulis ringens) eggs and larvae distributions off Peru, and to a comparable study conducted in the southern Benguela upwelling ecosystem.  相似文献   

20.
Examination of the phylogenetic structure of the family Candaciidae shows the genus Paracandacia to comprise a strongly modified branch emerging from the clade commonly denoted as Candacia. This has been confirmed by studying selected character phylogenies. It is argued that the resulting paraphyletic nature of Candacia auct., though in a cladistic context undesirable on theoretical grounds, has to be accepted as inevitable. Recent studies on molluscs and arthropods, viz., have demonstrated that the continuous origin of paraphyletic taxa from previously monophyletic ones is nothing but a naturally occurring process, intrinsically embodied in the course of evolution.  相似文献   

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