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icolls - Sustainable Tourism CRC

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

information about the variability in source and consumer isotopic signatures in the proximity of the mouth of<br />

both systems.<br />

The primary sources of carbon sampled were riparian vegetation, mangroves, BFPOM, BCPOM, attached<br />

and free-floating algae and seston (suspended particulate organic matter). Riparian vegetation and mangroves<br />

were hand collected, while BFPOM and BCPOM samples were collected by sifting benthic sediments through a<br />

series of graded sieves (250 µm - 500 µm - 1 cm). BFPOM samples were obtained from the 250 µm sieve and<br />

BCPOM samples were collected from the 500 µm sieve. Using a scalpel blade and brush, attached algae were<br />

carefully scraped from all available surfaces, including mangrove pneumatophores, rocks and woody debris.<br />

Aquatic insects, crustaceans and small fish were collected using a dip net and a small purse seine net. Fish<br />

were also collected in a larger seine net (measurements required) and unbaited fish traps. Sediment-dwelling<br />

organisms, including bivalve molluscs and polychaete worms, were collected using a yabby pump. Mobile<br />

consumers such as crabs were opportunistically hand collected wherever possible.<br />

Upon collection, all samples were immediately placed in individually labelled zip-lock bags and stored on<br />

ice. For the smaller organisms collected, this approach has been shown to enable them time to void their guts to<br />

expedite processing in the laboratory (Bunn & Boon 1993; Beaudoin et al. 2001). Samples were frozen for<br />

transportation back to the laboratory.<br />

Laboratory Sample Processing<br />

In the laboratory, samples of riparian vegetation, BFPOM, BCPOM, attached algae and mangroves were rinsed<br />

with distilled water to wash away dirt and debris. All samples were dried in an oven at 60°C for at least 48 hours.<br />

Dried samples were pulverised in a puck and ring grinding mill for approximately 3 minutes, or until the sample<br />

had been reduced to a fine powder. Ground samples were subsequently stored in 5 ml vials and frozen prior to<br />

analysis.<br />

Trichopteran larvae were removed from their cases upon collection. All aquatic macroinvertebrates were<br />

rinsed and dried before being ground using a mortar and pestle. Individuals were ground whole, but ground<br />

individuals were often subsequently pooled to ensure that sample size was sufficient to enable isotopic analyses.<br />

The exoskeletons of all aquatic crustaceans were removed to ensure that accumulated calcium carbonate did not<br />

influence carbon isotopic values (Mihuc & Toetz 1994; Leggett et al. 1999; Beaudoin et al. 2001).<br />

Analytical Methods<br />

Samples were analysed using a continuous flow-isotope ratio mass spectrometer (Micromass Isoprime<br />

EuroVector EA300, Manchester, UK) at Griffith University. Isotope ratios are expressed as either δ13C or δ 15 N<br />

and relate to the ratio of 13C:12C and 14N:15N, respectively. Values were calculated according to the following<br />

equation:<br />

δ 13 C or δ 15 N = [(Rsample / Rstandard) - 1] x 1000<br />

where Rsample is the isotopic ratio for the sample and Rstandard is the isotopic ratio of the standard (PeeDee<br />

belemnite carbonate for δ13C and atmospheric N for δ 15 N).<br />

For abundant taxa, nitrogen isotope signatures were statistically compared between samples from Tallows<br />

and Belongil Creeks using one way ANOVAs (Sokal & Rohlf 1999).<br />

Food web analyses were conducted using IsoSource mixing model software (Phillips & Gregg 2003).<br />

Trophic fractionations of carbon and nitrogen signatures were set at 0.2‰ and 1.5‰ respectively, based on<br />

values reported in the stable isotope literature (Peterson & Fry 1987; McCutchan, Lewis, Kendall & McGrath<br />

2003; Hadwen & Bunn 2004).<br />

Results<br />

Community Composition<br />

The composition of the Tallows Creek food web was distinctly different from that of Belongil Creek. There were<br />

generally more species collected from Tallows Creek, although some of these additional taxa reflected the status<br />

of Tallows Creek at the time of sampling (closed) more so than the influence of the STP inputs. For example,<br />

numerous freshwater macroinvertebrates were collected from Tallows Creek, highlighting the low salinity and<br />

absence of tidal fluctuations in the system. In contrast, moderate tidal exchange in Belongil Creek ensured that<br />

only estuarine/marine taxa were present at the time when collections were made.<br />

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