Luminescence dating of archaeosediments: A comparison of K-feldspar and plagioclase IRSL ages

IRSL single-aliquot dating of three feldspar fractions from a Howieson's Poort (SA) industry site has been investigated. In the case of the plagioclase fraction (ρ > 2.62 g cm^?3) equivalent dose is similar to that of the other fractions (i.e. ρ < 2.58 g cm^?3, high-K-feldspar; and 2.58 < ρ < 2.62 g cm^?3; low-K-feldspar). However, the g values measured for this fraction is such that the fading-corrected age is overestimated. The K content of each fraction was estimated by SEM. The DRC-corrected ages for the two lighter feldspar fractions are consistent with the archaeological interpretation. This study shows that reliable single-aliquot luminescence ages can be obtained using K-feldspar and Na-plagioclase.     

Mercury levels in selected bycatch fish species from industrial shrimp-trawl fishery in the SE Gulf of California

Baseline Hg concentration in bycatch fish from the SE Gulf of California were determined in muscle and liver of 19 species. Levels of Hg in muscle were compared with legal limits of this element in national and international legislation. Considering all fish species, mean concentrations in liver (2.458 ± 1.997 μg g⁻¹) were significantly higher (p < 0.05) than in muscle (0.993 ± 0.670 μg g⁻¹). The sequence of averaged Hg concentrations in most ichthyofauna was liver > muscle. Highest level of Hg in muscle (2.556 μg g⁻¹) and liver (7.515 μg g⁻¹) corresponded to Diapterus peruvianus and Ophioscion strabo, respectively. Considering muscle samples, none of the species had levels of Hg above the limit (1.0 μg g⁻¹ wet weight) in the Mexican legislation; with respect to the Japanese (0.4 μg g⁻¹ wet weight) and British (0.3 μg g⁻¹ wet weight) legislations, 26.3% and 31.6% of the species respectively, were above the corresponding limits.     

Natural antifouling compounds produced by a novel fungus Aureobasidium pullulans HN isolated from marine biofilm

A fungus, Aureobasidium pullulans, was isolated from marine biofilm and identified. A bioassay-guided fractionation procedure was developed to isolate and purify antifouling compounds from A. pullulans HN. The procedure was: fermentation broth—aeration and addition of sodium thiosulfate–graduated pH and liquid–liquid extraction—SPE purification—GC–MS analysis. Firstly, the fermentation broth was tested for its toxicity. Then it was treated with aeration and addition of sodium thiosulfate, and its toxicity was almost not changed. Lastly, antifouling compounds were extracted at different pH, the extract had high toxicity at pH 2 but almost no toxicity at pH 10, which suggested the toxicants should be fatty acids. The EC₅₀ of the extract against Skeletonema costatum was 90.9 μg ml⁻¹, and its LC₅₀ against Balanus amphitrete larvae was 22.2 μg ml⁻¹. After purified by HLB SPE column, the EC₅₀ of the extract against S. costatum was 49.4 μg ml⁻¹. The myristic and palmitic acids were found as the main toxicants by GC–MS.     

Correlations between electrical and elastic properties of solid–liquid composites with interfacial energy-controlled equilibrium microstructures

Electrical conductivity and seismic velocity are studied for plausible pore geometries in the Earth's interior for reliable quantitative analysis of experimental data such as seismic tomography and magnetotelluric explorations. Electrical conductivity of a two-phase system with equilibrium, interfacial energy-controlled phase geometry is calculated for the dihedral angles θ = 40°–100° that are typical for rock–aqueous fluid and θ = 20°–60° for rock–melt systems of lower crust and upper mantle for the case of tetrakaidecahedral grains. Electrical conductivity vs. seismic velocity correlations are acquired by combining of the simulated electrical conductivities with the seismic velocity calculated with the help of equilibrium geometry model Takei [Takei, Y., Effect of pore geometry on V_P/V_S: From equilibrium geometry to crack. J. Geophys. Res. 107 (2002): 10.1029/2001JB000522.] for the same pore geometries. The results show that electrical conductivity gradually decreases reaching zero when seismic velocities reach seismic velocities of intact rock for rock–melt systems, while for rock–aqueous fluid systems with θ ≥ 60° conductivity drops to zero at velocities up to 10% smaller. This can explain the seeming discrepancy of the low seismic velocity region, attributed to the high fluid fraction, and the low electrical conductivity of the same region, which is sometimes faced at collocated electromagnetic and seismic experiments.     

Analysis of aftershock sequences in South and Southeastern Spain

A probabilistic modeling is used to analyze the spatio-temporal behavior of eleven aftershock sequences occurred in South and Southeastern Spain. This study focuses on the analysis of two seismicity parameters: the b-value of the frequency-magnitude distribution, and the p-value, explaining the temporal decay rate of aftershocks. The estimated b values range between 0.77 ± 0.05 and 1.18 ± 0.10 close to the typical b-values of the aftershock frequency-magnitude relationship b ≈ 1.0. The estimated p-values range between 0.75 ± 0.03 and 1.43 ± 0.10 showing broad regimes of the temporal decay of aftershocks. The modified Bath’s law used to analyze the energy partitioning, suggests that a large fraction of the accumulated energy is released in the mainshock and relatively small fraction of energy is released during aftershock sequence, for example 80% of the total energy is released during the Mula 1999 mainshock, 88% during Bullas 2002 mainshock and 87% during La Paca 2005 mainshock. The fractal dimension D₂ is estimated using the correlation integral, and then used to derive the slip ratio, as the ratio of the slip occurred on primary fault segment to the total slip. For example, we obtained a slip ratio equal to 71% for the Mula 1999 aftershock sequence, 61% for the Bullas 2002 event, 58% for the La Paca 2005 aftershock, 50% for the Lorca 2011 sequence and 63% for the sequence triggered by the Gador 2002 mainshock.Finally, the correlations between the fractal dimension, the b-value and the p-value is analyzed, and the Aki’s relation D = 3b/c is discussed as well.     

Adsorption behaviour of dibutyl phthalate on marine sediments

Laboratory experiments were carried out to investigate the adsorption behaviour of dibutyl phthalate (DBP) on marine sediments collected from five different sites in Victoria Harbour, Hong Kong. DBP adsorption can be well described by the Langmuir isotherm. The maximum DBP adsorption capacity (Q_max) of the marine sediments ranges from 53 to 79 mg g⁻¹, which has a positive correlation with their organic content. Around 90% of the organic can be removed from the sediments with treatment by H₂O₂ oxidation, and the Q_max then decreases to a range between 13 and 22 mg g⁻¹. The black carbon content of the sediments has a much greater DBP adsorption capacity than does the natural organic matter of the sediments. The amount of DBP adsorbed on the sediments increases as the salinity of the marine water increases.     

Remote sensing based water quality monitoring in Chivero and Manyame lakes of Zimbabwe

Lakes Chivero and Manyame are amongst Zimbabwe’s most polluted inland water bodies. MEdium Resolution Imaging Spectrometry level 1b full resolution imagery for 2011 and 2012 were used to derive chlorophyll-a (chl_a) and phycocyanin (blue-green algae) concentrations using a semi-empirical band ratio model; total suspended matter (TSM) concentrations were derived from the MERIS processor. In-situ measured chl_a was used to validate the remotely sensed values. Results indicate that remote sensing measurements are comparable with in situ measurements. A strong positive correlation (R² = 0.91; MAE = 2.75 mg/m³ (8.5%)) and p < 0.01 (highly significant)) between measured and modeled chl_a concentrations was obtained. Relationships between optically active water constituents were assessed. Measured chl_a correlated well with MERIS modeled phycocyanin (PC) concentration (R² = 0.9458; p < 0.01 (highly significant)) whilst chl_a and TSM gave (R² = 0.7344; p < 0.05 (significant)). Modeled TSM and PC concentrations manifested a good relationship with each other (R² = 9047; p < 0.001 (very highly significant)). We conclude that remote sensing data allow simultaneous retrieval of different water quality parameters as well as providing near real time and space results that can be used by water managers and policy makers to monitor water bodies.     

Persistent organic pollutants and stable isotopes in pinnipeds from King George Island,Antarctica

In the present work, fat, skin, liver and muscle samples from Leptonychotes weddellii (Weddell seal, n = 2 individuals), Lobodon carcinophagus (crabeater seal, n = 2), Arctocephalus gazella (Antarctic fur seal, n = 3) and Mirounga leonina (southern elephant seal, n = 1) were collected from King George Island, Antarctica, and analysed for POPs (PCBs, organochlorine pesticides and PBDEs) and stable isotopes (δ¹³C and δ¹⁵N in all tissues but fat). PBDEs could be found in only one sample (L. weddellii fat). Generally, PCBs (from 74 to 523 ng g⁻¹ lw), DDTs (from 14 to 168 ng g⁻¹ lw) and chlordanes (from 9 to 78 ng g⁻¹ lw) were the prevailing compounds. Results showed a clear stratification in accordance with ecological data. Nonetheless, stable isotope analyses provide a deeper insight into fluctuations due to migrations and nutritional stress. Correlation between δ¹⁵N and pollutants suggests, to some degree, a considerable ability to metabolize and/or excrete the majority of them.     

Remediation studies of trace metals in natural and treated water using surface modified biopolymer nanofibers

In this study, remediation results of trace metals in natural water and treated water using three functionalized nanofiber mats of cellulose and chitosan are reported. The nanofiber materials, packed in mini-columns, were employed for the remediation of five toxic trace metals (Cd, Pb, Cu, Cr and Ni) from natural water samples. Trace metals in real water samples were undetectable as the concentrations were lower than the instrument’s detection limits of 0.27 × 10⁻³ (Cd) and 4.2 × 10⁻² (Pb) μg mL⁻¹, respectively. However, after percolation through the functionalised biosorbents in cartridges, detectability of the metal ions was enhanced. The starting volume of the natural water sample was 100 mL, which was passed through a column containing the nanofibers sorbent and the retained metals eluted with 5 mL of 2.0 M nitric acid. The eluate was analyzed for metals concentrations. An enrichment factor of 20 for the metals was realized as a result of the pre-concentration procedure applied to handle the determination of the metals at trace levels. The order of remediation of the studied metals using the nanofibers was as follows: chitosan/PAM-g-furan-2,5-dione < cellulose-g-furan-2,5-dione < cellulose-g-oxolane-2,5-dione. The modified biopolymer nanofibers were able to adsorb trace metals from the river water and treated water, thereby confirming their capability of water purification. These materials are proposed as useful tools and innovative approach for improving the quality of drinking for those consumers in small scale households.     

Toxicities of antifouling biocide Irgarol 1051 and its major degraded product to marine primary producers

Irgarol 1051 (2-methythiol-4-tert-butylamino-6-cyclopropylamino-s-triazine) is an algaecide commonly used in antifouling paints. It undergoes photodegradation which yields M1 (2-methylthio-4-tert-butylamino-6-amino-s-triazine) as its major and most stable degradant. Elevated levels of both Irgarol and M1 have been detected in coastal waters worldwide; however, ecotoxicity effects of M1 to various marine autotrophs such as cyanobacteria are still largely unknown. This study firstly examined and compared the 96 h toxicities of Irgarol and M1 to the cyanobacterium Chroococcus minor and two marine diatom species, Skeletonema costatum and Thalassiosira pseudonana. Our results suggested that Irgarol was consistently more toxic to all of the three species than M1 (96 h EC50 values: C. minor, 7.71 μg L⁻¹ Irgarol vs. >200 μg L⁻¹ M1; S. costatum, 0.29 μg L⁻¹ Irgarol vs. 11.32 μg L⁻¹ M1; and T. pseudonana, 0.41 μg L⁻¹ Irgarol vs. 16.50 μg L⁻¹ M1). Secondly, we conducted a meta-analysis of currently available data on toxicities of Irgarol and M1 to both freshwater and marine primary producers based on species sensitivity distributions (SSDs). Interestingly, freshwater autotrophs are more sensitive to Irgarol than their marine counterparts. For marine autotrophs, microalgae are generally more sensitive to Irgarol than macroalgae and cyanobacteria. With very limited available data on M1 (i.e. five species), M1 might be less toxic than Irgarol; nonetheless this finding warrants further confirmation with additional data on other autotrophic species.     

Distribution and source apportionments of polychlorinated biphenyls (PCBs) in mariculture sediments from the Pearl River Delta,South China

Surface and core sediments collected from six mariculture farms in the Pearl River Delta (PRD) were analyzed to evaluate contamination levels of polychlorinated biphenyls (PCBs). The ∑PCBs (37 congeners) concentrations ranged from 5.10 to 11.0 ng g⁻¹ (mean 7.96 ng g⁻¹) in surface and 3.19 to 22.1 ng g⁻¹ (mean 7.75 ng g⁻¹) in core sediments, respectively. The concentrations were significantly higher than that measured in the sediments of their corresponding reference sites, whereby the average enrichment percentages were 62.0% and 42.7% in surface and core sediments, respectively. Significant correlations (R² = 0.77, p < 0.05) of PCB homologue group proportions between fish feeds and surface mariculture sediments suggested that fish feed input was probably the main source for the enrichment of PCBs. Due to the fact that PCBs could be transferred along food chains, PCB contamination in fish feeds and mariculture sediments should not be overlooked.     

Removal of heavy metals from contaminated water using ethylenediamine-modified green seaweed (Caulerpa serrulata)

The demand for clean water is on the increase as the population increases. One of the ways to address the water shortage is to treat the polluted water through removal of the contaminants. The use of adsorbents for pollutant removal is one of the promising methods. Seaweed is an aquatic plant and its sorption ability for selected metals in water was investigated in this study. We report the performance of the seaweed (Caulerpa serrulata) before and after modification with ethylenediamine (EDA), on adsorption of copper, lead and cadmium in aqueous solution. The adsorption capacities for Cu, Cd and Pb were 5.27 mg g⁻¹, 2.12 mg g⁻¹ and 2.16 mg g⁻¹, respectively, with the EDA-modified seaweed, and 3.29 mg g⁻¹, 4.57 mg g⁻¹ and 1.06 mg g⁻¹, with the unmodified weed, respectively. The pH for maximum adsorption was found to be within the range of pH 4–pH 6. In a separate investigation, it was found that 0.1 g of dried seaweed leached 20 mg of dissolved organic carbon (DOC) using 100 ml of distilled-deionised water. The resulting solution was green. The leaching phenomenon contributes to secondary pollution. Modification of the seaweed with EDA reduced the DOC content by half (50%) and also removed the green colouration. Kinetic studies showed that the adsorbent was able to take up to 95% of the metals (in synthetic standard solutions) in less than 10 min. The adsorbed metals were then stripped using a solution of 0.5 M HNO₃ indicating that the adsorbent can be regenerated. In addition, the study revealed that modification improved the thermal stability of the adsorbent such that even when the temperature was raised to 1000 °C, more than 80% (compared to <50% for unmodified weed) of the modified adsorbent was not degraded, indicating that modification had a significant influence on the thermal stability of seaweed. The modified seaweed has been shown to have great potential for the removal of metals and DOC in polluted water. The modified adsorbent can therefore be applied for the removal of metals in polluted waters hence suitable for treatment of water for domestic consumption at a point of use.     

Lethal doses of oxbile,peptones and thiosulfate-citrate-bile-sucrose agar (TCBS) for Acanthaster planci; exploring alternative population control options

Effective control of outbreaks of Acanthaster planci represents the most immediate and practical intervention to reverse sustained declines in coral cover on reefs in the Indo-Pacific. This study explored the minimum doses of oxbile, oxgall, and thiosulfate-citrate-bile-sucrose agar (TCBS) that result in reliable and comprehensive mortality when injected into adult A. planci. The minimum doses required to induce 100% mortality among starfish (n = 10) were 4 g l⁻¹ of oxbile, 8 g l⁻¹ of oxgall and 22 g l⁻¹ of TCBS. Moreover, there was no evidence of unintended side effects for other coral reef organisms (e.g., scleractinian corals, echinoderms and fishes) when using oxbile, oxgall, or TCBS at minimum doses. The effectiveness of peptones in killing crown-of-thorns starfish was also tested, but inconsistency in the results revealed that these proteins are unreliable.     

Recycling of harbor sediment as lightweight aggregate

Sediment sampled from Taichung Harbor was mixed with local reservoir sediment at different weight ratios to prepare lightweight aggregate at 1050, 1100, and 1150 °C. A pressure of 3000 or 5000 psi was used to shape the powder mixtures into pellets before the heating processes. The results indicate that the leaching levels of trace metals from the lightweight aggregate samples are considerably reduced to levels less than Taiwan Environmental Protection Administration regulatory limits. Increasing final process temperature tends to reduce the bulk density and crushing intensity of lightweight aggregate with a concomitant increase in water sorption capability. Lightweight aggregate with the lowest bulk density, 0.49 g cm⁻³ for the 5000 psi sample, was obtained with the heating process to 1150 °C. Based on the X-ray absorption near edge structure results, FeSO₄ decomposition with a concomitant release of SO_x (x = 2, 3) is suggested to play an important role for the bloating process in present study.     

Importance of reversible attachment in predicting E. coli transport in saturated aquifers from column experiments

Drinking water wells indiscriminatingly placed adjacent to fecal contaminated surface water represents a significant but difficult to quantify health risk. Here we seek to understand mechanisms that limit the contamination extent by scaling up bacterial transport results from the laboratory to the field in a well constrained setting. Three pulses of Escherichia coli originating during the early monsoon from a freshly excavated pond receiving latrine effluent in Bangladesh were monitored in 6 wells and modeled with a two-dimensional (2-D) flow and transport model conditioned with measured hydraulic heads. The modeling was performed assuming three different modes of interaction of E. coli with aquifer sands: (1) irreversible attachment only (best-fit k_i = 7.6 day⁻¹); (2) reversible attachment only (k_a = 10.5 and k_d = 0.2 day⁻¹); and (3) a combination of reversible and irreversible modes of attachment (k_a = 60, k_d = 7.6, k_i = 5.2 day⁻¹). Only the third approach adequately reproduced the observed temporal and spatial distribution of E. coli, including a 4-log₁₀ lateral removal distance of ∼9 m. In saturated column experiments, carried out using aquifer sand from the field site, a combination of reversible and irreversible attachment was also required to reproduce the observed breakthrough curves and E. coli retention profiles within the laboratory columns. Applying the laboratory-measured kinetic parameters to the 2-D calibrated flow model of the field site underestimates the observed 4-log₁₀ lateral removal distance by less than a factor of two. This is promising for predicting field scale transport from laboratory experiments.     

Determination of selected persistent organic pollutants in wastewater from landfill leachates,using an amperometric biosensor

Landfill leachates that contain persistent organic pollutants (POPs) are a big threat to groundwater systems and are projected to have hazardous effects in the long term if proper management strategies of the landfills are not put in place by those responsible. Monitoring the levels of POPs in landfill leachates is very crucial. This work presents an amperometric biosensor for determination of selected POPs in landfill leachates. The biosensor is based on kinetic inhibition of horseradish peroxidase (HRP). The enzyme was immobilised by electrostatic attachment on a polyaniline-modified Pt electrode surface. Selected POPs inhibited HRP enzyme activity and the decrease in the enzyme activity was used to determine these environmental pollutants. Selected polybrominated diphenyl ethers (PBDEs), polybrominated biphenyls (PBBs) and polychlorinated biphenyls (PCBs) were the analytes of choice because they are commonly found in South Africa water systems. Limits of detection for the amperometric biosensor were established as 0.014, 0.018, 0.022, 0.016 and 0.019 μg l⁻¹ for BDE-100, PBB-1, PCB-1, PCB-28 and PCB-101, respectively. The HRP biosensor system gave different linear ranges for; BDE-100 (0.424–25.8 μg l⁻¹), PBB-1 (0.862–13.4 μg l⁻¹), PCB-1 (0.930–18.1 μg l⁻¹), PCB-28 (0.730–15.7 μg l⁻¹) and PCB-101 (0.930–27.1 μg l⁻¹). Inhibition studies on HRP biosensor response toward the reduction of H₂O₂ in the absence and presence of the selected POPs were carried out to investigate the inhibition kinetics and its mechanism. The results obtained indicated that the inhibition mechanism was competitive for PBDEs and non-competitive for biphenyls (PCBs and PBBs). The application of the biosensor was tested on wastewater samples obtained from landfill leachate for determination of selected POPs. The leachate samples were found to contain PCB-28 (0.28 ± 0.03 μg l⁻¹) and PCB-101 (0.31 ± 0.02 μg l⁻¹). The samples were also analysed by GC–MS as a cross-check method and the two sets of results were in close agreement.     

Sewage organic markers in surface sediments around the Brazilian Antarctic station: Results from the 2009/10 austral summer and historical tendencies

The discharge of sewage into the Antarctic marine environments by scientific stations has resulted in local changes in these pristine sites. To assess the distribution and concentration of sewage indicators from the Brazilian Antarctic station, sediments were sampled during the 2009/10 austral summer at four points (water depth of 20 and 60 m). Concentrations of faecal sterols and linear alkylbenzenes (LABs) ranged from <0.01 to 0.17 μg g⁻¹ and <1.0 to 46.5 ng g⁻¹ dry weight, respectively. Maximum concentration of faecal sterols was similar to the value previously calculated as the background level for this area (0.19 μg g⁻¹), and it is lower than the concentration observed in previous studies (1997–2008), whereas the LABs concentrations remained practically constant (35 ng g⁻¹). Despite the low concentrations of sewage markers, the permanent human activities in the region require monitoring programs to determine continuing trends and prevent the increase of anthropogenic impacts.     

Temporal and spatial variations of seismicity scaling behavior in Southern México

R/S analysis is used in this work to investigate the fractal correlations in terms of the Hurst exponent for the 1998–2011 seismicity data in Southern Mexico. This region is the most seismically active area in Mexico, where epicenters for severe earthquakes (e.g., September 19, 1985, M_w = 8.1) causing extensive damage in highly populated areas have been located. By only considering the seismic events that meet the Gutenberg–Ritcher law completeness requirement (b = 0.97, M_GR = 3.6), we found time clustering for scales of about 100 and 135 events. In both cases, a cyclic behavior with dominant spectral components at about one cycle per year is revealed. It is argued that such a one-year cycle could be related to tidal effects in the Pacific coast. Interestingly, it is also found that high-magnitude events (M_w ≥ 6.0) are more likely to occur under increased interevent correlations with Hurst exponent values H > 0.65. This suggests that major earthquakes can occur when the tectonic stress accumulates in preferential directions. In contrast, the high-magnitude seismic risk is reduced when stresses are uniformly distributed in the tectonic shell. Such cointegration between correlations (i.e., Hurst exponent) and macroseismicity is confirmed for spatial variations of the Hurst exponent. In this way, we found that, using the Hurst exponent standpoint, the former presumed Michoacan and the Guerrero seismic gaps are the riskiest seismic zones. To test this empirical finding, two Southern Mexico local regions with large earthquakes were considered. These are the Atoyac de Alvarez, Guerrero (M_w = 6.3), and Union Hidalgo, Oaxaca (M_w = 6.6), events. In addition, we used the Loma Prieta, California, earthquake (October 17, 1989, M_w = 6.9) to show that the high-magnitude earthquakes in the San Andreas Fault region can also be linked to the increments of determinism (quantified in terms of the Hurst exponent) displayed by the stochastic dynamics of the interevent period time series. The results revealed that the analysis of seismic activity by means of R/S analysis could provide further insights in the advent of major earthquakes.     

Polycyclic aromatic hydrocarbons in the coastal water,surface sediment and mullet Liza klunzingeri from northern part of Hormuz strait (Persian Gulf)

The concentrations of 16 polycyclic aromatic hydrocarbons (PAHs) were determined in mullet (Liza klunzingeri), water and sediment from northern part of Hormuz strait (Persian Gulf). The concentration levels of total PAHs in L. klunzingeri, water and sediment were 133.99–268.57 ng g⁻¹ dry weight, 3.12–5.88 ng l⁻¹ and 42.29–228.9 ng g⁻¹ dry weight, respectively. Based on isomer ratios, analysis of the PAHs source in the sediment demonstrated that the PAHs come from pyrogenic and petrogenic origin. Risk assessment showed PAHs threshold concentrations to occasionally be exceeded in the study area.     

Seasonal variability of primary production in a fjord ecosystem of the Chilean Patagonia: Implications for the transfer of carbon within pelagic food webs

We characterized the seasonal cycle of productivity in Reloncaví Fjord (41°30′S), Chilean Patagonia. Seasonal surveys that included measurements of gross primary production, community respiration, bacterioplankton secondary production, and sedimentation rates along the fjord were combined with continuous records of water-column temperature variability and wind forcing, as well as satellite-derived data on regional patterns of wind stress, sea surface temperatures, and surface chlorophyll concentrations. The hydrography and perhaps fjord productivity respond to the timing and intensity of wind forcing over a larger region. Seasonal changes in the direction and intensity of winds, along with a late-winter improvement in light conditions, may determine the timing of phytoplankton blooms and potentially modulate productivity cycles in the region.Depth-integrated gross primary production estimates were higher (0.4–3.8 g C m^?2 d^?1) in the productive season (October, February, and May), and lower (0.1–0.2 g C m^?2 d^?1) in the non-productive season (August). These seasonal changes were also reflected in community respiration and bacterioplankton production rates, which ranged, respectively, from 0.3 to 4.8 g C m^?2 d^?1 and 0.05 to 0.4 g C m^?2 d^?1 during the productive and non-productive seasons and from 0.05 to 0.6 g C m^?2 d^?1 and 0.05 to 0.2 g C m^?2 d^?1 during the same two periods. We found a strong, significant correlation between gross primary production and community respiration (Spearman, r=0.95; p<0.001; n=12), which suggests a high degree of coupling between the synthesis of organic matter and its usage by the planktonic community. Similarly, strong correlations were found between bacterioplankton secondary production and both gross primary production (Spearman, r=0.7, p<0.05, n=9) and community respiration (Spearman, r=0.8, p<0.05, n=9), indicating that bacterioplankton may be processing an important fraction (8–59%) of the organic matter produced by phytoplankton in Reloncaví Fjord. In winter, bacterial carbon utilization as a percentage of gross primary production was >100%, suggesting the use of allochthonous carbon sources by bacterioplankton when the levels of gross primary production are low. Low primary production rates were associated with a greater contribution of small cells to autotrophic biomass, highlighting the importance of small-sized plankton and bacteria for carbon cycling and fluxes during the less productive winter months. Fecal pellet sedimentation was minimal during this period, also suggesting that most of the locally produced organic carbon is recycled within the microbial loop. During the productive season, on the other hand, the area exhibited a great potential to export organic matter, be it to higher trophic levels or vertically towards the bottom.