Natural and cultured populations of the mangrove oyster Saccostrea palmula from Sinaloa, Mexico, infected by Perkinsus marinus

The mangrove oyster Saccostrea palmula coexists with the pleasure oyster Crassostrea corteziensis in coastal lagoons of northwest Mexico. Recent discovery of Perkinsus marinus infecting the pleasure oyster in the region prompted evaluation of S. palmula as an alternative P. marinus host. An analysis to determine the possible presence of P. marinus in natural and cultured populations of S. palmula at four coastal lagoons in Sinaloa, Mexico was carried out during October-November 2010. Tissues from apparently healthy S. palmula were evaluated using Ray's fluid thioglycollate method (RFTM), which revealed a Perkinsus sp. to be present in all four locations at 6.7-20.0% prevalence. Histopathological analysis of these specimens showed tissue alterations and parasite forms consistent with moderate P. marinus infection, which was confirmed by ribosomal non-transcribed spacer (NTS)-based PCR assays on DNA samples from oysters positive by RFTM and histology. DNA sequencing of amplified NTS fragments (307 bp) produced a sequence 98-100% similar to GenBank-deposited sequences of the NTS from P. marinus. Fluorescent in situ hybridization for Perkinsus spp. and P. marinus corroborated the PCR results, showing clear hybridization of P. marinus in host tissues. This is the first record of P. marinus infecting a species from genus Saccostrea and the first record of the parasite from coastal lagoons in Sinaloa, Mexico.     

Spatial and temporal changes in the nekton of the Terminos Lagoon, Campeche, Mexico

This study describes the current state of the nektonic communities in Terminos Lagoon in relation to the main environmental factors, and documents variations in number of fish species, dominance and abundance, compared to studies performed in 1980. Information on several environmental factors (temperature, salinity, oxygen, pH and transparency) in the Terminos Lagoon between October 1997 and March 1999 allowed the classification of the lagoon into five zones or subsystems. The hydrological characteristics of these subsystems showed spatial differences compared with studies carried out during the 1980s. During the study period, the number of fish species was 105, compared with 154 species reported in the 1980s. Five fish assemblages were identified and appeared to be associated with the five zones or subsystems. Five fish species considered important based on their abundance in the lagoon during the 1980s declined in numbers: pig fish Orthopristis chrysoptera , Atlantic croaker Micropogonias undulates , striped burrfish Chilomycterus schoepfi , spotted seatrout Cynoscion nebulosus and Gulf toadfish Opsanus beta . Six fish species, previously of minor importance, however, were very abundant: star drum Stellifer lanceolatus , Atlantic anchoveta Cetengraulis edentulus , gafftopsail catfish Bagre marinus , sand seatrout Cynoscion arenarius , striped mojarra Eugerres plumieri and ground croaker Bairdiella ronchus . Among the dominant species, the silver croaker Bairdiella chrysoura and the sea bream Archosargus rhomboidalis experienced significant changes in average abundance and distribution patterns. These changes were probably related to the impact of human activities in the Terminos Lagoon and natural variability.     

Application of a multiplex PCR for the detection of protozoan pathogens of the eastern oyster Crassostrea virginica in field samples

Populations of eastern oysters Crassostrea virginica along the east coast of North America have repeatedly experienced epizootic mass mortality due to infections by protozoan parasites, and molecular diagnostic methodologies are fast becoming more widely available for the diagnosis of protozoan diseases of oysters. In this study we applied a modified version of an existing multiplex polymerase chain reaction (PCR) for detection of the eastern oyster parasites Haplosporidium nelsoni, H. costale and Perkinsus marinus from field-collected samples. We incorporated primers for DNA quality control based on the large subunit ribosomal RNA (LSU rRNA) gene of C. virginica. The multiplex PCR (MPCR) simultaneously amplified genomic DNA of C. virginica, and cloned DNA of H. nelsoni, P. marinus and H. costale. In field trial applications, we compared the performance of the MPCR to that of the conventional diagnostic techniques of histopathological tissue examination and the Ray/Mackin fluid thioglycollate medium (RMFT) assay. A total of 530 oysters were sampled from 18 sites at 12 locations along the east coast of the United States from the Gulf of Mexico to southern New England. The modified MPCR detected 21% oysters with H. nelsoni, 2% oysters with H. costale, and 40% oysters with P. marinus infections. In comparison, histopathological examination detected H. nelsoni and H. costale infections in 6 and 0.8% oysters, respectively, and the RMFT assay detected P. marinus infection in 31% oysters. The MPCR is a more sensitive diagnostic assay for detection of H. nelsoni, H. costale, and P. marinus, and incorporation of an oyster quality control product limits false negative results.     

Influence of salinity on prevalence of the parasite Loxothylacus panopaei in the xanthid Panopeus obesus in SW Florida

This study was conducted to examine the potential influence of salinity, a proxy for freshwater inflow, on the prevalence of the castrator parasite Loxothylacus panopaei on saltmarsh mud crabs Panopeus obesus on SW Florida oyster reefs. Spatial and seasonal patterns of the presence of potential host crabs and the prevalence of the parasite were assessed in the Caloosahatchee, Estero, and Faka Union estuaries. Lift nets (1 m2) containing 5 1 of oyster clusters were deployed on intertidal reefs at 3 sites along the salinity gradient of each estuary. Nets were deployed during 3 seasonally dry and 3 seasonally wet months for a period of 30 d. P. obesus densities tended to increase downstream in higher salinity waters, with crabs being absent from the upper station in the Caloosahatchee during both seasons and absent from the upper station of the Faka Union during wet months. Parasite prevalence was reduced upstream in each estuary during wet months compared to dry months, and for those estuaries that experienced higher relative levels of freshwater inflow. Furthermore, parasite prevalence was positively correlated with the mean salinity of capture of host crabs. Based on the distribution of P. obesus and the above patterns related to salinity, it appears that freshwater inflow and seasonal rains might regulate the prevalence of this parasite in SW Florida by creating spatiotemporal, low salinity refuges for its host.     

Prevalence of Perkinsus marinus (dermo), Haplosporidium nelsoni (MSX), and QPX in bivalves of Delaware's inland bays and quantitative, high-throughput diagnosis of dermo by QPCR

Restoration of oyster reef habitat in the Inland Bays of Delaware was accompanied by an effort to detect and determine relative abundance of the bivalve pathogens Perkinsus marinus, Haplosporidium nelsoni, and QPX. Both the oyster Crassostrea virginica and the clam Mercenaria mercenaria were sampled from the bays. In addition, oysters were deployed at eight sites around the bays as sentinels for the three parasites. Perkinsus marinus prevalence was measured with a real-time, quantitative polymerase chain reaction (PCR) methodology that enabled high-throughput detection of as few as 31 copies of the ribosomal non-transcribed spacer region in 500 ng oyster DNA. The other pathogens were assayed using PCR with species-specific primers. Perkinsus marinus was identified in Indian River Bay at moderate prevalence ( approximately 40%) in both an artificial reef and a wild oyster population whereas sentinel oysters were PCR-negative after 3-months exposure during summer and early fall. Haplosporidium nelsoni was restricted to one oyster deployed in Little Assawoman Bay. QPX and P. marinus were not detected among wild clams. While oysters in these bays have historically been under the greatest threat by MSX, it is apparent that P. marinus currently poses a greater threat to recovery of oyster aquaculture in Delaware's Inland Bays.     

Selection of phytoplankton associations in Lake Balaton,Hungary, in response to eutrophication and restoration measures,with special reference to the cyanoprokaryotes

Seasonal and spatial patterns of aquatic primary production were compared in a tidal creek (Estero Pargo) bordered by mangroves and open waters of Terminos Lagoon, Mexico. Comparisions were made during a 17-month period in 1990–91 that spanned dry, rainy, and storm or 'Norte' seasons. Annual net primary productivity was 478 g C m-2 yr-1 in the lagoon and 285 g C m-2 yr-1 in the tidal creek. In some months, there were significant differences in primary production between the two sites. In both areas, the highest productivity occurred in summer at the start of the rainy season (June 1991), and the lowest production occurred during the dry season from February to May. Aquatic primary production was lower during the dry season of 1991 in comparison to 1990, possibly related to unusually low precipitation during 1991. Seasonal changes in water column productivity were correlated to variations in light and precipitation. The effect of runoff from mangrove forests was assessed by serial additions of surface water from a fringe forest to bottle incubations of lagoon water. Small additions of mangrove water stimulated primary production in lagoon waters during all seasons. The net productivity was extremely sensitive to aliquot volume; small amounts (0.3 and 1.7% of total volume) were stimulatory, increasing rates by > 50% in 7 of 12 experiments. The greatest effect occurred in September, 1990, when productivity tripled after an amendment with 1 ml (0.3% by volume) of mangrove water. Additions greater than 3% of total volume generally led to reduction in net productivity probably due to the inhibitory effect of humic substances. In many tropical systems, tidal exchange of estuarine waters with mangrove forests is likely to be important to enhancing water column productivity by exporting organic nutrients and other growth-enhancing substances to the estuary. This revised version was published online in July 2006 with corrections to the Cover Date.     

Effects of triclosan on growth, viability and fatty acid synthesis of the oyster protozoan parasite Perkinsus marinus

Perkinsus marinus, a protozoan parasite of the Eastern oyster Crassostrea virginica, has severely impacted oyster populations from the Mid-Atlantic region to the Gulf of Mexico coast of North America for more than 30 yr. Although a chemotherapeutic treatment to reduce or eliminate P. marinus from infected oysters would be useful for research and hatchery operations, an effective and practical drug treatment does not currently exist. In this study, the antimicrobial drug triclosan 5-chloro-2-(2,4 dichlorophenoxy) phenol, a specific inhibitor of Fab1 (enoyl-acyl-carrier-protein reductase), an enzyme in the Type II class of fatty acid synthetases, was tested for its effects on viability, proliferation and fatty acid synthesis of in vitro-cultured P. marinus meronts. Treatment of P. marinus meront cell cultures with concentrations of > or = 2 microM triclosan at 28 degrees C (a temperature favorable for parasite proliferation) for up to 6 d stopped proliferation of the parasite. Treatment at > or = 5 microM at 28 degrees C greatly reduced the viability and fatty acid synthesis of meront cells. Oyster hemocytes treated with > or = 20 microM triclosan exhibited no significant (p < 0.05) reduction in viability relative to controls for up to 24 h at 13 degrees C. P. marinus meronts exposed to > or = 2 microM triclosan for 24 h at 13 degrees C exhibited significantly (p < 0.05) lower viability relative to controls. Exposure of P. marinus meronts to triclosan concentrations of > or = 20 microM resulted in > 50% mortality of P. marinus cells after 24 h. These results suggest that triclosan may be effective in treating P. marinus-infected oysters.     

Non-specific immune parameters of brood Indian major carp Labeo rohita and their seasonal variations

Different non-specific immune parameters and their seasonal changes in brood Indian major carp Labeo rohita reared in two major freshwater aquaculture regions of India viz. West Bengal and Orissa were investigated. It was undertaken for 2 consecutive years and included three main seasons of a year such as summer (March-May), rainy (July-September) and winter (November-January). Total serum protein, albumin and globulin levels were not significantly different throughout the year (p>0.01). Serum lysozyme and myeloperoxidase activities were lower (7.26+/-0.87mg/ml and, 0.54+/-0.11 OD, respectively) in winter as compared to any other season of the year. The bacterial agglutination titer was higher (p<0.01) in the rainy season (8.70+/-1.70) compared to summer and winter seasons (3.40+/-0.60 and 4.00+/-0.89, respectively). Haemagglutination and haemolytic activities did not vary (p>0.01) throughout the year. In blood smears, lymphocyte percentage was higher (75-80%) as compared to those of neutrophil (10-15%) and monocytes (5-10%) but eosinophilic granulocytes were present only in few cases. The differential leucocyte count did not vary significantly (p>0.05) in any season. This study indicated that certain non-specific immune parameters of this species can be modulated at certain times of the year.     

Protease activity in the plasma of American oysters, Crassostrea virginica, experimentally infected with the protozoan parasite Perkinsus marinus

Perkinsus marinus is responsible for disease and mortality of the American oyster, Crassostrea virginica. To investigate the interactions between P. marinus and oyster hemocytes, protease activity was measured in plasma of oysters collected 4 hr, 24 hr, 4 days, and 2 mo after experimental infection with P. marinus. A significant increase in protease activity was observed in oyster plasma 4 hr after injection with P. marinus, followed by a sharp decrease within 24 hr. Gelatin-impregnated gel electrophoresis showed the presence of 2 major bands (60 and 112 kDa) and 3 less prevalent bands (35, 92, and 200 kDa) with metalloproteinaselike activity in the plasma of noninfected oysters. Additional bands in the 40- to 60-kDa range, corresponding to P. marinus serine proteases, were observed in oyster plasma at early time points after infection. A transient, but significant, decrease in the activity of oyster metalloproteinases was observed at early time points after infection. Coincubation of oyster plasma with P. marinus extracellular products resulted in a decrease in oyster metalloproteinases and several P. marinus proteases. This study provides insights into the role of proteases in the pathogenesis of Dermo disease.     

Comparison of in vitro-cultured and wild-type Perkinsus marinus. III. Fecal elimination and its role in transmission

Perkinsus marinus, a pathogen of the eastern oyster Crassostrea virginica, is transmitted directly among oysters. Previous studies found viable P. marinus parasites in the feces and pseudofeces of oysters within hours of injection with parasites, suggesting that the parasite may be voided from live oysters and subsequently dispersed in the water column. The experiments described here were designed to quantify P. marinus shed in the feces and pseudofeces of experimentally infected oysters. The results indicated that parasites were shed in 2 phases. A 'decreasing' phase occurred within 2 wk of challenge and before net parasite proliferation began in the host. An 'increasing' phase occurred after P. marinus had begun replicating. The quantity of P. marinus recovered in the feces and pseudofeces of exposed oysters was only about 5 % of the dose administered. In vitro-cultured P. marinus were eliminated at a greater rate than wild-type P. marinus and the fraction discharged was not associated with culture phase. Oysters that were continuously dosed with P. marinus in their food gradually lost the ability to discard the parasite in pseudofeces. The quantity of P. marinus shed in feces of infected oysters was correlated with both the P. marinus body burden and subsequent survival time, suggesting that noninvasive fecal counts could predict infection intensity and survival. The results indicate that in an epizootic, shedding of P. marinus via feces is relatively small compared to the potential number released by cadavers of heavily infected oysters, but that fecal discharge may be important in transmission before infections become lethal.     

Length–weight relationships of fish species associated with the mangrove forest in the southwestern Terminos Lagoon,Campeche (Mexico)

Length–weight relationships (LWR) were calculated for 18 species representing 11 families of fishes. A total of 958 fish specimens from the southwestern Terminos Lagoon, Campeche (Mexico), several of which had none or few LWRs available in FishBase, were sampled (except December) using a shrimp otter trawl net from September 2003 to August 2004. Sample sizes ranged from seven Mugil curema and Archosargus probatocephalus individuals to 250 Eugerres plumieri.     

A quantitative competitive polymerase chain reaction assay for the oyster pathogen Perkinsus marinus

A quantitative competitive polymerase chain reaction (QCPCR) assay was developed for the oyster parasite Perkinsus marinus. PCR primers for the rRNA gene region of P. marinus amplified DNA isolated from P. marinus but not from Perkinsus atlanticus, Crassostrea virginica, or the dinoflagellates Peridinium sp., Gymnodinium sp., or Amphidinium sp. A mutagenic primer was used to create a competitor plasmid molecule identical to the P. marinus target DNA sequence except for a 13-bp deletion. Both P. marinus and competitor DNA amplified with equivalent efficiencies. Each of 25 oysters was processed by 5 P. marinus diagnostic methods--Ray's fluid thioglycollate medium (FTM) tissue assay, FTM hemolymph assay, whole oyster body burden assay, QCPCR of combined gill and mantle (gill/mantle) tissue, and QCPCR of hemolymph. The QCPCR assay enabled detection of 0.01 fg of P. marinus DNA in 1.0 microg of oyster tissue. QCPCR of gill/mantle tissue or hemolymph as well as the body burden assay detected infections in 24 of 25 oysters. Ray's FTM tissue assay detected only 19 infections. The FTM hemolymph assay detected only 22 infections. Regression analysis of QCPCR results and FTM results indicated that the QCPCR assays were effective in quantitating P. marinus infections in oyster tissues.     

Effects of plasma from bivalve mollusk species on the in vitro proliferation of the protistan parasite Perkinsus marinus

The in vitro culture of the Eastern oyster parasite Perkinsus marinus has provided a unique opportunity to examine its susceptibility to putative recognition and effector defense mechanisms operative in refractory bivalve species. In this study, we report the effect of supplementing the culture medium with plasma from: (1) uninfected to heavily infected Eastern oysters; (2) oyster species considered to be disease-resistant; and (3) bivalve mollusk species that are naturally exposed to the parasite but show no signs of disease. We also examined in vitro the interaction between hemocytes from Crassostrea virginica and C. gigas and P. marinus trophozoites. Our results revealed a significant decrease (32%) in proliferation of P. marinus in the presence of plasma from heavily infected C. virginica oysters. The inhibitory effects were less pronounced with plasma from moderately infected and uninfected oysters. In contrast, plasma from C. rivularis and C. gigas enhanced P. marinus proliferation. Proliferation was significantly reduced in media supplemented with plasma from Mytilus edulis, Mercenaria mercenaria, and Anadara ovalis. The highest inhibitory activity was apparent in M. edulis, for which 5% plasma-supplemented medium reduced growth by 35% relative to the controls. M. edulis active component(s) was heat-stable, yet pronase-sensitive. The significantly higher uptake of live P. marinus trophozoites by hemocytes from C. virginica, relative to those from C. gigas, suggests a certain level of specificity in the recognition/endocytosis of the parasite by its natural bivalve host species.     

Analysis of the effects of Perkinsus marinus proteases on plasma proteins of the Eastern oyster (Crassostrea virginica) and the Pacific oyster (Crassostrea gigas).

We employed two in vitro buffer systems to determine the potential pathogenic effects of Perkinsus marinus serine proteases on the plasma proteins of the eastern oyster (Crassostrea virginica) and the Pacific oyster (Crassostrea gigas). Specifically, this study characterized the oyster plasma protein targets of P. marinus proteases. Additionally, protease-specific inhibitory activity was revealed upon comparison of artificial (PBS) and endogenous (plasma-based) diluents employed during protease digestions. It was found that a C. virginica plasma protein of approximately 35 kDa was eliminated when a standard buffer (PBS) was used as a diluent; however, this protein was preserved when a low-molecular-weight, plasma-based, diluent was used. The results strongly indicate that low-molecular-weight inhibitors of P. marinus proteases are present in oyster plasma. A control (nonparasitic) serine protease, alpha-chymotrypsin, was employed to ascertain the specificity of the protease inhibitors. Although alpha-chymotrypsin possesses ample proteolytic activity for C. virginica plasma proteins, the anti-proteases could specifically inhibit only P. marinus proteases. Such specificity of anti-protease activity is not uncommon among low-molecular-weight serine proteases. The hemolymph target protein was isolated by 2D electrophoresis and isoelectrically isolated for further characterization by N-terminal amino acid sequencing.     

Systematic evaluation of factors controlling Perkinsus marinus transmission dynamics in lower Chesapeake Bay

The transmission of Perkinsus marinus in eastern oysters Crassostrea virginica in relation to water temperature, host oyster mortality, and water-column abundance of anti-P. marinus antibody-labeled cells was systematically examined for 20 mo at a site in the lower York River, Virginia, USA. Uninfected sentinel oysters were naturally exposed to the parasite at 2 wk intervals throughout the course of the study to determine the periodicity and rates of parasite transmission. The timing and magnitude of disease-associated oyster mortalities in a local P. marinus-infected oyster population were estimated by monitoring a captive subset of the local oyster population. Flow cytometric immunodetection methods were employed to estimate the abundance of P. marinus cells in water samples collected 3 times each week. The acquisition of P. marinus infections by na?ve sentinel oysters occurred sporadically at all times of the year; however, the highest incidence of infection occurred during the months of August and September. This window of maximum parasite transmission coincided with the death of infected hosts within the captive local oyster population. Counts of antibody-labeled cells ranged from 10 to 11900 cells l(-1), with the highest abundances in July and August coincident with maximum summer temperatures. A statistically significant relationship between water-column parasite abundance and infection-acquisition rate was not observed; however, highest parasite-transmission rates in both years occurred during periods of elevated water-column abundance of parasite cells. These results support the prevailing model of P. marinus transmission dynamics by which maximum transmission rates are observed during periods of maximum P. marinus-associated host mortality. However, our results also indicate that transmission can occur when host mortality is low or absent, so alternative mortality-independent dissemination mechanisms are likely. The results also suggest that atypically early-summer oyster mortality from Haplosporidium nelsoni infection, at a time when infections of P. marinus are light, has a significant indirect influence on P. marinus transmission dynamics. Elimination of these hosts prior to late-summer P. marinus infection-intensification effectively reduces the overall number of P. marinus cells disseminated.     

Seasonal growth of Mugil liza Valenciennes, 1836 in a tropical estuarine system

Seasonal changes in the abiotic factors and cyclical events – with the reproduction diagnosed by the gonadosomatic index and the energy status diagnosed by the condition index – were estimators of seasonal growth for juvenile and adult lebranche mullets, Mugil liza, during the rainy and dry seasons in a tropical estuarine system of the western south Atlantic. Fish were collected monthly by gillnets of different mesh sizes. Salinity, water temperature (°C) and dissolved oxygen (%) were measured using a multiparameter. Daily rainfall data (mm) were obtained from the National Institute of Meteorology. Seasonal rings were identified and counted in the sagittae otoliths. Relative Marginal Increment (RMI) was calculated to determine the seasonal growth rate. Gonadosomatic Index (GSI) and Condition Index (CI) were assessed separately for juveniles and adults by anova , with time (month) M. liza growth is controlled by annual cycles of biological and abiotic processes. Using general linear models, the seasonal growth rate of M. liza was well predicted by body condition and rainfall for juveniles, and by salinity for adults. Seasonal variation was observed in the Mundaú Lagoon, with rainfall directly or indirectly being the main seasonal factor influencing the cyclical biological fish processes of M. liza.     

Nutrient content of seagrasses and epiphytes in the northern Gulf of Mexico: Evidence of phosphorus and nitrogen limitation

We examined C:N:P ratios of seagrass leaves and epiphytic algae from the eastern shoreline of Grand Bay (Alabama, USA) and the entire shoreline of Big Lagoon (Florida, USA) during the summer of 2001 and March 2003, and used contour plotting of N:P ratios in both locations to examine spatial trends in our data. Results indicated phosphorus limitation for seagrass and epiphytes in each bay. In addition, C:N, C:P, and N:P ratios in both locations showed differences between summer and wintertime values for seagrasses; however, the only epiphytic elemental ratios to differ were C:P and N:P ratios in Grand Bay. Within Grand Bay, phosphorus limitation was stronger in epiphytes than seagrasses, with the largest amount of variation in N:P ratios occurring adjacent to the only developed land on the shoreline. In Big Lagoon, two distinct areas were present in N:P contour plots: the eastern end of the bay that was influenced by water from the Gulf of Mexico and Santa Rosa Sound, and the western end of the bay that was most influenced by Perdido Bay and a developed area along the northern shoreline. Detection of phosphorus limitation within Big Lagoon was not surprising, as both input sources to Big Lagoon are known to be low in phosphorus. However, phosphorus limitation in Grand Bay was unexpected, as both “feeder systems” (Mobile Bay and the Mississippi Sound) have high ambient phosphorus levels. As a result, C:N:P ratios from seagrasses and epiphytes may not accurately reflect ambient nutrient levels in Grand Bay due to decreased availability of some forms of phosphorus or increased competition for the uptake of phosphorus. Overall, our C:N:P analysis suggested that not only was P limitation greater than N limitation in Grand Bay and Big Lagoon, but patterns of nutrient limitation varied both temporally and geographically for inter- and intra-bay comparisons.     

Human impacts and the status of water quality in the Bundala RAMSAR wetland lagoon system in Southern Sri Lanka

The brackish coastal wetlands in the Bundala National Park, the only RAMSAR site of southern Sri Lanka, are an important waterfowl habitat and economic zone. Bundala Lagoon, one of the three key lagoons of the Bundala wetlands, remains largely intact and relatively pristine, but the other two interconnected lagoons, namely, Embilikala and Malala, are impacted by drainage from 25.6 km² of upstream agricultural lands. Seasonal variations of water quality of the three lagoons and the key processes affecting water quality and quantity in these lagoons were studied during three agricultural seasons, to better understand the characteristics of the system. Bundala Lagoon, which was not affected by agriculture, recorded the highest ammonia and total nitrogen concentrations and the lowest phosphorus levels. Higher phosphorus levels in Embilikala Lagoon were related to the upstream agricultural activities with 65% of its total phosphorus measured being reactive phosphorous. Phosphorus additions occurred during the early months of the paddy cultivating seasons. Processes affecting the water quality of the Embilikala-Malala lagoon system included agricultural drainage, livestock additions, and breaching of the sand bar between Malala Lagoon and the sea. The salinity level of the Bundala Lagoon was higher than the others due to the connection to the sea, salt farms in the western part, and less dilution of salt from relatively low surface runoff and rainwater. All three lagoons reported pH levels conducive to most aquatic species. The primary production by phytoplankton in the lagoons of the Bundala wetland was phosphorus limited regarding their ratios of nitrogen to phosphorus. This study provides an overview of the present status of the lagoons of the wetland. Further work is needed to evaluate the impact of the external nutrient and water inputs on the flora and fauna of the lagoon environments. Suitable management practices to ensure the sustainability of the lagoon ecosystem can be derived through this increased understanding.     

Rainfall and labile carbon availability control litter nitrogen dynamics in a tropical dry forest

N cycling in tropical dry forests is driven by rainfall seasonality but the mechanisms involved are not well understood. We studied the seasonal variation in N dynamics and microbial biomass in the surface litter of a tropical dry forest ecosystem in Mexico over a 2-year period. Litter was collected at 4 different times of the year to determine changes in total, soluble, and microbial C and N concentrations. Additionally, litter from each sampling date was incubated under laboratory conditions to determine potential C mineralization rate, net N mineralization, net C and N microbial immobilization, and net nitrification. Litter C concentrations were highest in the early-dry season and lowest in the rainy season, while the seasonal changes in N concentrations varied between years. Litter P was higher in the rainy than in the early-dry season. Water-soluble organic C (WSOC) and water-soluble N concentrations were highest during the early- and late-dry seasons and represented up to 4.1 and 5.9% of the total C and N, respectively. NH₄⁺ and NO₃⁻ showed different seasonal and annual variations. They represented an average 23% of soluble N. Microbial C was generally higher in the dry than in the wet seasons, while microbial N was lowest in the late-dry and highest in the early-rainy seasons. Incubations showed that lowest potential C mineralization rates and C and N microbial immobilization occurred in rainy season litter, and were positively correlated to WSOC. Net nitrification was highest in rainy season litter. Our results showed that the seasonal pattern in N dynamics was influenced by rainfall seasonality and labile C availability, and not by microbial biomass. We propose a conceptual model to hypothesize how N dynamics in the litter layer of the Chamela tropical dry forest respond to the seasonal variation in rainfall.