Physical water column observations during summer breeze winds

During summer seasons (from 2012 to 2015) high resolution observation were performed in the Civitavecchia coastal area (Northern Tyrrhenian sea, west coast). All sampling was carried out from a small boat (5m rigid inflatable) starting in the early morning typically around 06:00 a.m. , and lasting from 2 to 8 h, depending on the weather conditions. The purposes of the experiment was to observe the variations of both the coastal circulation and the water column in response to rotation of 180 ° in the wind direction. During surveys both current measurements and yo-yo time series were performed. Current data were acquired using an ADCP SonTeck (500 Khz, sampling interval from 20sec to 60 sec, average interval 50% sampling, cell thickness 1 meter) and the yo-yo time series employing a small instrument package (CTD). The CTD contained an Idronaut 316 Plus and a SeaPoint fluorometer. The sampling rate for the CTD was 10Hz, profiling with the CTD was done by allowing the instrument package to free-fall, at an average descent rate of 1 m/s. During the summer 2012, the sampling plan consisted in four stations spaced a quarter of a mile (St. 1 - 10 m; St. 2 - 20 m; St. 3 - 30 m; and St. 4 - 40 m), in which yo-yo time series were performed with an interval of 20 min. In order to study fluorescence of Chlorophyll a pathes distribution in coastal zone. Breeze induced circulation was the goal of the following summers surveys, in these current measurements and yo-yo time series were performed moored at a depth of 40 m. Offshore station (St. 1 -40m) has been chosen to perform measurement, basis of previously observations (2012 sampling surveys). It was decided as wind driven circulation and mixing phenomena are less influenced by seabed than the other stations. Acquired data have been processed by NEMO SeaDataNet software.

Shallow water marine sediment bacterial community shifts along a natural CO2 gradient in the Mediterranean Sea Off vulcano, Italy

The effects of increasing atmospheric CO(2) on ocean ecosystems are a major environmental concern, as rapid shoaling of the carbonate saturation horizon is exposing vast areas of marine sediments to corrosive waters worldwide. Natural CO(2) gradients off Vulcano, Italy, have revealed profound ecosystem changes along rocky shore habitats as carbonate saturation levels decrease, but no investigations have yet been made of the sedimentary habitat. Here, we sampled the upper 2 cm of volcanic sand in three zones, ambient (median pCO(2) 419 µatm, minimum Omega (arag) 3.77), moderately CO(2)-enriched (median pCO(2) 592 µatm, minimum Omega (arag) 2.96), and highly CO(2)-enriched (median pCO(2) 1611 µatm, minimum Omega (arag) 0.35). We tested the hypothesis that increasing levels of seawater pCO(2) would cause significant shifts in sediment bacterial community composition, as shown recently in epilithic biofilms at the study site. In this study, 454 pyrosequencing of the V1 to V3 region of the 16S rRNA gene revealed a shift in community composition with increasing pCO(2). The relative abundances of most of the dominant genera were unaffected by the pCO(2) gradient, although there were significant differences for some 5 % of the genera present (viz. Georgenia, Lutibacter, Photobacterium, Acinetobacter, and Paenibacillus), and Shannon Diversity was greatest in sediments subject to long-term acidification (>100 years). Overall, this supports the view that globally increased ocean pCO(2) will be associated with changes in sediment bacterial community composition but that most of these organisms are resilient. However, further work is required to assess whether these results apply to other types of coastal sediments and whether the changes in relative abundance of bacterial taxa that we observed can significantly alter the biogeochemical functions of marine sediments.

The effects of growth phase and salinity on the hydrogen isotopic composition of alkenones produced by coastal haptophyte algae

The isotopic fractionation of hydrogen during the biosynthesis of alkenones produced by marine haptophyte algae has been shown to depend on salinity and, as such, the hydrogen isotopic composition of alkenones is emerging as a palaeosalinity proxy. The relationship between fractionation and salinity has previously only been determined during exponential growth, whilst it is not yet known in which growth phases natural haptophyte populations predominantly exist. We have therefore determined the relationship between the fractionation factor, alpha alkenones-water, and salinity for C37 alkenones produced in different growth phases of batch cultures of the major alkenone-producing coastal haptophytes Isochrysis galbana (strain CCMP 1323) and Chrysotila lamellosa (strain CCMP 1307) over a range in salinity from ca. 10 to ca. 35. alpha alkenones-water was similar in both species, ranging over 0.841-0.900 for I. galbana and 0.838-0.865 for C. lamellosa. A strong (0.85 <= R**2 <= 0.97; p < 0.0001) relationship between salinity and fractionation factor was observed in both species at all growth phases investigated. This suggests that alkenone dD has the potential to be used as a salinity proxy in coastal areas where haptophyte communities are dominated by these coastal species. However, there was a marked difference in the sensitivity of alpha alkenones-water to salinity between different growth phases: in the exponential growth phase of I. galbana, alpha alkenones-water increased by 0.0019 per salinity unit (S 1), but was less sensitive at 0.0010 S 1 and 0.0008 S 1 during the stationary and decline phases, respectively. Similarly, in C. lamellosa alpha alkenones-water increased by 0.0010 S 1 in the early stationary phase and by 0.0008 S 1 during the late stationary phase. Assuming the shift in sensitivity of alpha alkenones-water to salinity observed at the end of exponential growth in I. galbana is similar in other alkenone-producing species, the predominant growth phase of natural populations of haptophytes will affect the sensitivity of the alkenone salinity proxy. The proxy is likely to be most sensitive to salinity when alkenones are produced in a state similar to exponential growth.