19.06.2013 Views

Preprint volume - SIBM

Preprint volume - SIBM

Preprint volume - SIBM

SHOW MORE
SHOW LESS

Create successful ePaper yourself

Turn your PDF publications into a flip-book with our unique Google optimized e-Paper software.

Genoa<br />

Sestri Levante<br />

Pre-print Volume – Oral presentations<br />

Topic 3: INTEGRATED COASTAL ZONE MANAGEMENT<br />

Ligurian<br />

Sea<br />

15° E<br />

40° N<br />

Fig. 1 – Map of the sampling location.<br />

Localizzazione geografica del sito di campionamento.<br />

Sagittal otoliths were extracted under a stereomicroscope, cleaned and stored to dry.<br />

One otolith from each pair was aged, mounted on glass slide, and ground (with 3M<br />

Imperial lapping film) to expose the core. Otoliths were then rinsed, sonicated for 10<br />

min in de-ionized water, and analyzed using a LA-ICPMS (laser ablation inductively<br />

coupled plasma mass spectrometer) for 8 elements (Li, Mg, Mn, Zn, Sr, Ba, Pb and Hg;<br />

the values of Mn and Hg were consistently below the detection limits and therefore<br />

excluded from the data analyses). The LA-ICPMS system was calibrated using 610 and<br />

612 glasses. Calcium was used as internal standard to take into account variation in<br />

ablation and aerosol efficiency. Three replicates from each core were sampled by three<br />

sequential pits vertically collected (Ruttenberg et al., 2008) using a spot size of ~28<br />

μm. Three additional pits were collected in the juvenile region (~40-50 μm far from the<br />

core; Cermeño et al., 2006) to assess potential differences in the microchemical<br />

composition of the otolith related to the ontogenetic development (Elsdon &<br />

Gillanders, 2005). Prior to analysis, samples were pre-ablated to remove any surface<br />

contamination (laser at 50% power). The putative differences between ‘core’ and<br />

‘juvenile’ otolith sectors, and among otoliths (using otolith × element matrices) were<br />

analysed using two-way permutational multivariate analysis of variance<br />

(PERMANOVA; Anderson, 2001). The sampling design consisted of 2 factors: “core”<br />

vs “juvenile” otolith sectors (C vs J; fixed factor with 2 levels) and ‘otolith’ (Ot;<br />

random and orthogonal). Multivariate analyses were based on dissimilarity matrices<br />

based on Euclidean distances and log(x+1) transformed data. nMDS of centroids for<br />

each otolith (separating cores and juvenile sectors) was used to visualize the pattern<br />

observed (Clarke & Warwick, 2001). The SIMPROF (similarity profile) test,<br />

associated to cluster analysis (PRIMER 6 package; Clarke & Gorley, 2006), was used<br />

to test the null hypothesis that our set of otolith cores, not a priori divided into groups,<br />

do not differ from each other in microchemical composition. The SIMPROF test was<br />

run after having split anchovy samples into age groups. Otoliths corresponding to<br />

specimens 3 (n=10) and 4 years old (n=3) were too scarce numerically and were<br />

excluded from the statistical analyses.<br />

Results - Otoliths of European anchovy from Sestri Levante showed different<br />

microchemical patterns when cores were compared with juvenile otolith sectors (Fig.<br />

2). PERMANOVA test revealed that cores and juvenile sectors were significantly<br />

different (d.f.: 1; pseudo-F: 1766.98; P

Hooray! Your file is uploaded and ready to be published.

Saved successfully!

Ooh no, something went wrong!