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The water column : Physics , Nutrients , Organic matter

Sediments and interstitial waters : Granulometry, Physical and chemical characteristics of  interstitial waters, Nutrients fluxes, Organic matter mineralization

Physical and chemical characteristics of  interstitial waters

L. Charpy

 

peeper                               

 

Materiel and methods

 

Sampling

staint.gif (15646 octets)

8 stations were surveyed in the lagoon of Tikehau atoll: 3 in 1987 (1,4 et 8) et 6 in 1993 (2,3,5,6,7,8). Station 1 is located close to the internal reef flat. Stations 2 and 3 have been chosen because of their leeward and windward locations from a pinnacle with respect to the prevailing wind direction. Stations 4, 5 and 6 exhibit depths similar to the average depth of the lagoon (25 m) while stations 7 and 8 are located in the deepest part of the lagoon.

 

We used the in situ peeper sampling method described by Hesselein (1976). The peepers were inserted in the sediment and left on the site for at least 15 days in order to equilibrate the initial pore water with the interstitial medium. According to the size of the peeper chambers (3 or 10 ml), the spatial resolution is either 1 cm or 2.5 cm. These chambers were covered with a Biodyne A membrane (pore size = 0.2 µm).

 

Analysis

The pH was determined at room temperature (T = 22 °C)  on submicrosamples (500 µl) using an Ingold micro-electrode and the Hansson's calibration method des­cribed by Almgren et al. (1975) with a precision of ± 0.01 pH unit. 

Gran's potentiometric titration was used for alkalinity measurements (Stumm and Morgan 1981). 

The accuracy was ± 0.5 %.  Standard colorimetric procedures were used for nutrient analysis (SiO2, NH4 and PO4) and total dissolved sulfide (SO4), adapted for submicro samples (Merck Spectroquant methods; sample volume: 0.5 or 1 ml, precision ±4%).

A known volume of the ZnS suspension is used to develop the colorimetric analysis of H2S using the conventional methylene-blue method with a precision of  ± 3 %. 

Ca were analyzed by conventional AAS procedures with a precision of 5 %.

 

Results 

 

Pore water profiles of H2S, pH, alcalinité et calcium

h2s.gif (5120 octets)
Fig. 2

H2S (Fig. 2) appears either a few millimeters or 2 centimeters below the sediment water interface (SWI) at stations 5 and 8, while this redox limit is located between 3  and 5 cm below the SWI at stations 1, 2 and 4. The highest concentrations (365 µM) are observed at station 5, 13 cm below the SWI.

SO4 concentration profile is available only at station 8 (Fig. 2). It regularly decreases with the depth in the sediments.

ph.gif (6872 octets)

pH 
in pH unity 

All the stations exhibit the same general characteristics:

  • The pH immediately decreases below the SWI (1cm inside the sediment).

  • The calcium measured at station 8, shows a relatively constant concentration between 9 and 12.5 mM.

  • Maximum of alcalinity are observed between 5 and 15 cm inside the sediment at stations 3, 5, 6 et 8 (data of 1987) and between 0 and 5 cm inside the sediment at stations 2 and 8 (data of 1993).

caalka.gif (6792 octets)

calcium and alcalinity 
in mM

 

Pore water profiles of nutrients concentrations

  • The PO4 profiles 

po4.gif (10082 octets)

We observe :

  • an increasing concentration from the SWI to a maximum ranging from 2 to 6 µM located between 4 and 6 cm downward at stations 2, 3, 6 and 8.

  • an increasing concentration from the SWI to a maximum ranging from 2 to 5 µM located between 10 and 25 cm downward at stations 1, 4, 5 and 7.

  • The Si profiles

We observe :

  • a regular but minor increase of the concentration with depth along the sediment core at stations 2 and 8.

  • an increasing concentration going through a maximum, followed by a regular decrease at stations 2, 5, 6 and 7. The highest concentrations being observed at stations 5 (59 µM) and 7 (32 µM).

si.gif (8669 octets)

  • The NH4 profiles

nh4.gif (9437 octets)

We observe :

  • either a regular increase as at stations 1, 2 and 6

  • or a mid-depth maximum concentrations as seen at stations 5 (102 et 180 µM) and 7 (101µM).

 

Relation between the depth and the nutrients

The integrated concentrations in the upper layer of 20 cm of  the sediments,  expressed in cm2 of PO4 and NH4, are correlated to the depths of the stations (R=0.79, n = 13 for PO4 and R = 0.73, n = 11 for NH4). The sedimentation rates of the organic matter from the water column is certainly one of factors of the influence of the depth on the nutrients concentrations in the interstitial waters. Consequently the fluxes calculated of  PO4 and NH4 are also correlated to the depth (respectively R= 0.73 and R= 0.73).

selspro.gif (4349 octets)

 

 

This page was based on :

Charpy-Roubaud C., Charpy L., Sarazin G. (1996) Diffusional nutrient fluxes at the sediment-water interface and organic matter mineralization in an atoll lagoon (Tikehau, Tuamotu Archipelago, French Polynesia). Mar Ecol. Progr. ser. 132: 181-190

 

References :

Hesslein RH (1976) An in situ sampler for close interval pore water studies. Limnol Oceanogr 21: 912-924

update : 07/10/08

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