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icolls - Sustainable Tourism CRC

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ECOLOGY, THREATS AND MANAGEMENT OPTIONS FOR SMALL ESTUARIES AND ICOLLS<br />

Sampling Methods<br />

38<br />

Table 7: Physical properties recorded at the time of sampling for each location<br />

Belongil Ck. (High Tide) Belongil Ck (Low Tide) Tallows Ck<br />

Date/Time 10/12/03. 11am 10/12/03. 1.30pm 15/12/03. 11am<br />

pH 7.91 7.98 7.9<br />

DO 6.74ppM 6.03ppM 5.21<br />

Temp. 24.6 o C 28.6 o C 26.4 o C<br />

Cond. 47.9mS 44.6mS 10.2mS<br />

Salinity 29.0ppK 26.9ppK 5.62ppK<br />

Fish were collected using a 20m seine net with 6mm mesh trawled over predominately sandy substrates in close<br />

proximity to littoral vegetation and submerged structures and debris. Seine trawls were conducted between<br />

9:00am and 2:00pm on each sampling occasion. Captured fish were removed from the net after each trawl and<br />

placed immediately into an ice-slurry for transportation back to the laboratory for processing. Sampling of<br />

potential prey items was also conducted using a dip net and a small seine net with a mesh size < 2mm. All<br />

components of the food web were sampled across a range of habitat types representing those available at each<br />

site. Sampling protocols were identical to those outlined in Chapters 2 and 3.<br />

Sample Processing<br />

The total length of each fish was measured and recorded in the laboratory to the nearest 5mm at the conclusion<br />

of each field collection. The gut contents of each fish were removed and preserved in 4% formalin. Gutted fish<br />

were frozen for proposed tissue sampling for stable isotope analyses of trophic relations (following the methods<br />

detailed in Chapters 2 and 3). Two days prior to microscopic investigation the preserved stomach contents were<br />

transferred to a solution of 70% ethanol.<br />

Before ingested items were removed, the gut cavity contents were dried with blotting paper and excess<br />

ethanol allowed to evaporate before being weighed in grams to two decimal places. The entire contents of the<br />

digestive tract were removed by dissection and placed in a Petri dish with 70% ethanol. The contents were then<br />

sorted taxonomically under a Wild M3Z dissecting microscope (6.5-40X). Prey items were recorded under nine<br />

broad dietary categories adapted from existing literature and personal observation of possible prey items found in<br />

the food web sampling.<br />

Dietary Analysis<br />

Gut contents analyses<br />

The dietary analyses utilised three main parameters proposed by Hyslop (1980). These methods have been<br />

widely adopted for the analysis of teleost diets (Edgar & Shaw 1995; Hyndes, Platell & Potter 1997; Sarre,<br />

Platell & Potter 2000; Schafer et al. 2002) and therefore facilitated comparisons between studies. The percent<br />

frequency of occurrence of each dietary item in the stomachs of all fish and the relative contributions of each<br />

dietary item to the number and volume in the stomach of each fish were calculated. Volumes of dietary<br />

categories were calculated indirectly, whereby the items within each diet category were pooled and their<br />

percentage contribution estimated against a standard 1mm grid. This method takes into account the stomach<br />

fullness of each individual analysed (Hyslop 1980). Gut content analyses were restricted to those individuals<br />

whose stomachs contained dietary items at the time of capture. However, individuals with no gut contents were<br />

still included in the isotopic analyses of diet composition, as this method uses muscle tissue as an integrated<br />

measure of diet over a longer period of time than instantaneous gut content methods (Jones & Waldron 2003).<br />

Since volumetric data best represents the relative importance of each dietary category, especially when a<br />

combination of both large and small prey items are eaten that may over- or under-emphasise their importance<br />

(Hyslop 1980), subsequent analyses were performed using only volumetric data for each dietary category. The<br />

use of the volumetric contribution also allows amorphous food items such as algae and detritus to be included for<br />

analysis (Hyslop 1980). Furthermore, comparison of diet reconstructions using gut contents and stable isotope<br />

methods is facilitated using this parameter (Jones & Waldron 2003).<br />

Indices of diversity (Shannon-Wiener, H`) and evenness (J) were calculated to examine the dietary breadth of<br />

each species at each location (Marshall & Elliot 1997). These indices have been widely used to assess teleost

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