Page 7 - Caruso_Zaccone_2000
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LAP ACTIVITY IN AQUATIC ECOSYSTEMS  957




                  (a)
                 3                                    6              (b)
                                                                    3                                 6
               log µg C l –1  h –1  2                 4 2  log cfu   ml –1  log µg C l –1  h –1  2 1  4 2  log cfu   ml –1


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                    F MAM J      J  A S ON D     J  M                  F MAM J     J A S ON D J     M

                  (c)                                                (d)
                 3                                   6              3                                 6
               log µg C l –1  h –1  2                4 2  log cfu   ml –1  log µg C l –1  h –1  2 1   4 2  log cfu   ml –1


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                    F MAM J      J  A S ON D     J  M                 F MAM J      J A S ON D J     M


                  (e)                                                 (f)
                 3                                   6              3                                  6
               log µg C l –1  h –1  2                4 2  log cfu   ml –1  log µg C l –1  h –1  2      4 2  log cfu   ml –1



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          Fig. 5 Oliveri-Tindari lagoon: monthly distribution of LAP (& in log mg C l ÿ1 h ) and viable plate counts (& in log cfu ml ) found in
          Marinello (a), Mergolo (b), Verde (c), Fondo Porto (d), Porto (e) and Nuovo (f) ponds


          coast (Fig. 1) and is characterized by a strong geomorphism  ine in¯uence (Porto, Fondo Porto and Nuovo). In Porto,
          which makes it a very natural dynamic ecosystem. During  Mergolo and Fondo Porto ponds, the activity followed a
          1997/98, surface samples were drawn monthly from six  trend with a peak value in spring and a gradual decrease
          ponds (Marinello, Mergolo, Verde, Fondo Porto, Porto and  towards the other seasons; this decrease in LAP levels was
          Nuovo). The integrated analysis of heterotrophic bacterial  more pronounced in Marinello pond (about three times). A
          abundance, aminopeptidase activity and organic content  different pattern was recorded in Verde and Nuovo ponds,
          highlighted the ecological diversi®cation between the  which showed a peak in summer coinciding with the late
          ponds, probably caused by a progressive con®nement from  phytoplankton bloom and a decrease from autumn to win-
          the sea (Leonardi et al. 1998b). In fact, the monthly distri-  ter, particularly in Verde pond (about 10 times). ANOVA
          bution of LAP (Fig. 5) showed the highest levels of activity  test values also con®rmed the statistical signi®cance of dif-
          in the most brackish ponds (Marinello and Verde with  ferences among the ponds due to seasons (F ˆ 1194, P <
          peaks, respectively, of 31385 and 26122 mg C l ÿ1 h ÿ1  in  001, n ˆ 24), whereas differences in LAP, depending on
          June), which are located far from the sea and are mostly  the variable `site', were not statistically signi®cant (F ˆ
          subject to terrestrial in¯uence. Temporal variations of the  165, P < 001).
          enzyme activity, analysed on a seasonal scale, were more  Viable heterotrophic bacteria displayed in all the ponds a
          evident in these ponds (Table 3); in contrast, less temporal  seasonal course, ranging from maximum values detected in
                                                                                     ÿ1
                                                                              5
          variability and low levels of activity (max leucine 3994 mg  summer (386  10 cfu ml , in Verde pond) to lowest
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                                                                                       2
                ÿ1
          C l ÿ1  h ) characterized those ponds more subject to mar-  densities (minimum 250  10 cfu ml , in Mergolo) in
          = 2000 The Society for Applied Microbiology, Journal of Applied Microbiology, 89, 951ÿ959
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