Impacts of glacial discharge on the primary production in a Greenlandic fjord.

Subglacial discharge from marine-terminating glaciers in Greenland injects large volumes of freshwater and suspended sediment into adjacent fjord environments. Although the discharge itself is nutrient poor, the formation of meltwater plumes can enhance marine biological production by stimulating upwelling of nutrient-rich fjord water. Despite the importance of meltwater discharge to marine ecosystems, little is known of the quantitative impact of discharge processes on phytoplankton growth, including the effects of local plumes, fjord-wide stirring and mixing, and suspended sediments on net primary production (NPP). Here, we report simulations of Bowdoin Fjord in northwestern Greenland using coupled non-hydrostatic ocean circulation and lower-trophic level ecosystem models, developed using field data. Our findings demonstrate that subglacial discharge plays a crucial role in NPP by stirring and mixing the entire fjord water system, which has a greater effect on NPP than local plume upwelling. Sensitivity tests suggest a 20% increase in NPP under conditions of enhanced discharge anticipated in the future. However, if glacier discharge and retreat exceed critical levels, NPP is predicted to decline by 88% relative to present values. This pattern reflects the negative impact of increased sediment flux on photosynthesis and weakened fjord stirring and mixing resulting from shallower outlet depths.

Age distribution of Antarctic Bottom Water off Cape Darnley, East Antarctica, estimated using chlorofluorocarbon and sulfur hexafluoride.

Chlorofluorocarbon (CFC) and sulfur hexafluoride (SF6) were used to investigate the timescale of Antarctic Bottom Water (AABW) that spreads off Cape Darnley (CD) in East Antarctica. The age of the AABW was estimated based on the observed SF6/CFC-12 ratio while taking into account tracer dilution by Lower Circumpolar Deep Water. Along the western canyons off CD and the ~ 3000 to 3500 m isobaths, the bottom water age was < 5 years, reflecting the spread of newly formed CD Bottom Water. Higher ages of ~ 8 years obtained for areas east of CD and > 20 years in the northwestern offshore region indicate inflows of AABW through the Princess Elizabeth Trough and Weddell Sea Deep Water, respectively. This study determined the age distribution in the region off CD, where three different types of AABW spread.

Expression of the theta class GST isozyme, YdfYdf, in low GST dogs.

We have reported the existence of low glutathione S-transferase (GST) dogs whose GST activity to 1,2-dichloro-4-nitrobenzene (DCNB) as a substrate (GST-D activity) is quite low, and have also reported significant individual differences in dog liver GST-D activity. The dogs were classified as "low", "middle", or "high" GST dogs based on their GST-D activity. In the present study, in order to investigate the causes of quite low GST-D activity in low GST dogs and the individual differences in dog GST-D activity, glutathione (GSH) conjugation of DCNB was kinetically analyzed. Moreover, liver cytosolic proteins whose expression levels were significantly lower in low GST dogs than in high GST dogs were identified by two-dimensional difference gel electrophoresis (2D-DIGE) and LC tandem mass spectrometry (LC/MS/MS). Interestingly, Vmax values for this reaction well reflected their GST-D activities in all groups, i.e. they were 3.8, 80.6, and 169.2 nmol/min/mg protein in the low, middle, and high GST dogs, respectively. However, Km values were almost the same (260.0-283.7 microM) among these groups. These suggest that GSH conjugation of DCNB should be catalyzed by the same enzyme in all the dogs, and individual differences in the GST-D activity should be the result of individual differences in the expression level of the GST isozyme, which catalyzes conjugation of DCNB. In 2D-DIGE, the expression levels of the two protein spots were significantly lower in the low GST dogs than in the high GST dogs. Positive good correlation (r > 0.800) was observed between GST-D activity and expression levels of these two protein spots. Moreover, expression levels were quite low in low GST dogs. These two proteins were both identified as the theta class GST isozyme, YdfYdf, which specifically catalyzes GSH conjugation of DCNB in dog livers. In the present study, we present two novel findings based on an enzyme kinetic study and protein-expression analysis: (1) GSTYdfYdf is expressed at quite a low level in the liver of low GST dogs, and (2) individual differences in dog liver GST-D activity would be due to individual differences in the expression level of GSTYdfYdf. Considering these findings, low GST dogs might have high susceptibility, including an unexpected toxicity at abnormal exposure to chemicals metabolized by GSTYdfYdf.

Low glutathione S-transferase dogs.

Liver and kidney glutathione S-transferase (GST) activities to 1,2-dichloro-4-nitrobenzene (DCNB) as a substrate (GST-D activities) were measured in 280 dogs from five different breeders, and significant individual differences in this activity were observed in both organs. Interestingly, 34 out of the 280 dogs (i.e. 12.1%) were those in which liver GST-D activities were less than 10 nmol/min per mg cytosolic protein, "low GST dogs", and the other dogs were classified as "middle" and "high" GST dogs for which the liver GST-D activities were 10-80 and >80 nmol/min per mg protein, respectively, and occurred at similar percentages (41.4% for the middle GST dog and 46.4% for the high GST dog). Furthermore, the existence of the low GST dogs was not limited to one particular breeder. There was a good correlation (r=0.910) between the liver and kidney GST-D activities, showing low activity in not only the liver but also the kidney in the low GST dogs. Although liver GST activity to 1-chloro-2,4-dinitrobenzene as a substrate (GST-C activity), catalyzed by various GST isozymes in dogs, was significantly correlated with liver GST-D activity, GST-C activity showed more than 450 nmol/min per mg protein even in the low GST dogs. There was no significant difference in cytochrome P450 content, 7-ethoxycoumarin O-deethylase activity or UDP-glucuronosyltransferase activity to p-nitrophenol as a substrate between low GST dogs and the other dogs. Finally, remarkably high plasma concentrations of DCNB were observed in the low GST dogs after single doses of DCNB at 5 or 100 mg/kg. The individual differences in GST-D activity are probably attributable to the content and/or activity of the theta class GST isozyme Yd(f)Yd(f) since it has been reported that glutathione conjugation of DCNB is specifically catalyzed by GSTYd(f)Yd(f) in dogs. In conclusion, we identified a number of low GST dogs in which the GST-D activities were not observed either in vivo or in vitro. The feasibility of using a single low dose of DCNB to phenotype dogs based on GST-D activity was confirmed. It was also suggested that low GST dogs have high susceptibility, including unexpected toxicity or abnormal exposure, to chemicals metabolized by GSTYd(f)Yd(f).