Absorption coefficients of particulate matter and chlorophyll a concentrations at time series station OLIPAC

Spectral absorption coefficients of total particulate matter ap (lambda) were determined using the in vitro filter technique. The present analysis deals with a set of 1166 spectra, determined in various oceanic (case 1) waters, with field chl a concentrations ([chl]) spanning 3 orders of magnitude (0.02-25 mg/m**3). As previously shown [Bricaud et al., 1995, doi:10.1029/95JC00463] for the absorption coefficients of living phytoplankton a phi (lamda), the ap (labda) coefficients also increase nonlinearly with [chl]. The relationships (power laws) that link ap (lambda) and a phi (lambda) to [chl] show striking similarities. Despite large fluctuations, the relative contribution of nonalgal particles to total absorption oscillates around an average value of 25-30% throughout the [chl] range. The spectral dependence of absorption by these nonalgal particles follows an exponential increase toward short wavelengths, with a weakly variable slope (0.011 ± 0.0025/nm). The empirical relationships linking ap (lambda) to ([chl]) can be used in bio-optical models. This parameterization based on in vitro measurements leads to a good agreement with a former modeling of the diffuse attenuation coefficient based on in situ measurements. This agreement is worth noting as independent methods and data sets are compared. It is stressed that for a given ([chl]), the ap (lambda) coefficients show large residual variability around the regression lines (for instance, by a factor of 3 at 440 nm). The consequences of such a variability, when predicting or interpreting the diffuse reflectance of the ocean, are examined, according to whether or not these variations in ap are associated with concomitant variations in particle scattering. In most situations the deviations in ap actually are not compensated by those in particle scattering, so that the amplitude of reflectance is affected by these variations.

Distribution of macrozooplankton at time series station MIGZOO-1

Vertical distributions and diel migrations of the main species of micronekton, four euphausiids, one mysid, one decapod and three fishes, were described in detail in the 0-1000 m water column on a fixed station in the Northwestern Mediterranean Sea. The euphausiids Euphausia krohni and Thysanopoda aequalis, the decapod Gennadas elegans and, to a lesser extent, the fish Argyropelecus hemigymnus were shown to perform clear diel vertical migrations. Results of horizontal hauls at a given depth around sunrise and sunset showed a marked diurnal symmetry of the migratory cycles, particularly for E.krohni, T.aequalis and G.elegans. The behaviour of the euphausiid Nematoscelis megalops was more complex: it presented a repetitive bimodal day distribution and only part of its population migrated. As very weak or non-migrators we found the euphausiid Stylocheiron longicorne and the bathypelagic mysid Eucopia unguiculata, for which migration concerned only some of the older individuals. The fishes Cyclothone braueri and Cyclothone pygmaea appeared to be non-migrants. As depth increased, C.braueri was replaced by C.pygmaea, with maximum concentrations at 350-550 and 550-700 m depth, respectively.

Distribution of macrozooplankton at time series station MIGZOO-4

A large population of the colonial pelagic tunicate Pyrosoma atlanticum occurred in April 1991 in offshore waters of the Ligurian Sea (Northwestern Mediterranean). The high numbers of colonies caught allowed their vertical distribution and diel migration in the 0-965 m water column to be described as a function of their size. Daytime depths and amplitudes of the migration were correlated with colony size. The amplitude of the migration ranged from 90 m for 3-mm-length colonies to 760 m for 51-mm-length colonies, with a mean amplitude of 410 m for the whole population, all sizes pooled. The results of horizontal hauls at a given depth around sunrise and sunset showed a marked diurnal symmetry of the migratory cycle relative to noon, and that migration of the population was not cohesive. For example, the larger the colonies, the later after sunset they reached the upper layers during their upward migration.