Effects of mechanical macrophyte control on suspended sediment concentrations in streams

Suspended sediment (SS) is an important pollutant in freshwater ecosystems and can be detrimental to fish communities. Although macrophytes mediate sediment deposition, little effort has been put into determining how their removal affects sediment resuspension. The present study examined the immediate and long-term impacts of mechanical macrophyte removal on SS concentrations in streams. The results of this study suggest that bed disturbance during mechanical excavation of macrophytes significantly increases SS in the short term, and concentrations were found to increase by as much as 15,687 mg L^–1 immediately after macrophyte removal. Significant long-term (77 day) increases in SS were also observed, indicating that without macrophytes, disturbed material is continually resuspended after excavation by fluvial processes. These results demonstrate that macrophyte removal can result in SS levels that have previously been shown to harm fish, and indicate that this activity may be more detrimental to fish than previously thought.     

Land use,associated eel production,and abundance of fish and crayfish in streams in Waikato,New Zealand

Abstract

The density and biomass of fish and crayfish, and the production of eels, was compared among streams in native forest, exotic forest, and pasture. Populations were estimated by multiple‐pass electroshocking at 11 sites in hill‐country streams in the Waikato region, North Island. Three sites were in native forest, four in exotic forest, and four in pasture. Length of stream sampled at each site was 46–94 m (41–246 m² in area), and catchment areas up stream of the sites ranged from 0.44 to 2.01 km².

A total of 487 fish were caught. The species were longfinned and shortfinned eels, banded kokopu, Cran's and redfinned bullies, and common smelt. Eels were the most abundant fish in all three land‐use types, and shortfinned eels were more abundant at pastoral sites (mean density 1.11 fish m^?2) than longfinned eels (mean density 0.129 fish m^?2). Banded kokopu were present only at forested sites. Mean fish densities were greater at pastoral sites (1.55 fish m^?2) than under either native forest (0.130 fish m^?2) or exotic forest (0.229 fish m^?2). Mean fish biomass was also greater at pastoral sites (89.7 g m^?2) than under native forest (12.8 g m^?2) or exotic forest (19.3 g m^?2). Longfinned eels made a greater contribution to the fish biomass at all sites than did shortfinned eels. Densities of crayfish were high (0.46–5.40 crayfish m^?2), but were not significantly different between land‐use types. Crayfish biomass ranged from 1.79 to 11.2 g m^?2. Total eel production was greater at pastoral sites (mean 17.9 g m^?2 year¹) than at forest sites (mean 2.39 gm^?2 year^?1).     

Reduced abundance of banded kokopu (Galaxias fasciatus) and other native fish in turbid rivers of the North Island of New Zealand

Laboratory experiments demonstrated that migrant juvenile banded kokopu (Galaxias fasciatus Gray) were more sensitive to suspended sediment (SS) than other native fish species. If juvenile migrants avoid waters made turbid by SS and their recruitment to adult habitats up stream is reduced, then adult abundance may decline in turbid rivers. To test this, we compared the abundance of diadromous native fish between turbid and clear rivers. The duration (% time) for which SS concentrations exceeded 120 mg litre^‐1 (a critical level from laboratory experiments) during the migration season (August‐December) was estimated for over 150 New Zealand river sites. Turbid rivers were defined as those where SS concentrations exceeded 120 mg litre^‐1 for over 20% of the time and clear rivers as those where SS concentrations exceeded 120 mg litre^‐1 for less than 10% of the time. Eight turbid rivers and seven clear ones were identified where sufficient data on SS and native fish populations existed to permit a comparison. The mean occurrence of banded kokopu was reduced by 89.5% in turbid rivers and, although other diadromous fish species were also less common, banded kokopu was most affected. Densities of adult banded kokopu were also significantly lower in optimal stream habitats in three turbid compared with three matched clear rivers. We therefore concluded that the abundance of adult banded kokopu was reduced in turbid rivers and propose that this is because of reduced recruitment of juveniles in turbid rivers.     

Book reviews

Theory and management of tropical fisheries. Edited by D. Pauly and G. I. Murphy. Proceedings of the ICLARM/CSIRO Workshop on the Theory and Management of Tropical Multispecies Stocks. 12–21 January 1981, Cronulla, Australia. 1982. 360 p. $US21.50 surface; hardbound.

Animals of the estuary shore : illustrated guide and ecology. By Malcolm B. Jones, 1983. University of Canterbury publication No. 32. 162p., 140 figures, 11 keys. ISBN 0900–392–32–0 (soft cover, spiral bound). Price NZ$7.50.

Numerical ecology. By L. Legendre and P. Legendre, 1983. Elsevier Scientific Publishing Company, Amsterdam. $US83.00.

The control of oil pollution (revised edition). Edited by J Wardley‐Smith. Graham & Trot‐man Limited, London. 1983. 285 p., 98 figures, 17 tables. ISBN 0.86010 3382. £19.00/$US35.00.

Physical oceanography in Australia. Edited by J. Imberger. Reprinted from the Australian Journal of Marine and Freshwater Research, Volume 34, 1–230, 1983. CSIRO, Melbourne 1983.     

Petrogenesis of the Swartruggens and Star Group II kimberlite dyke swarms,South Africa: constraints from whole rock geochemistry

Thirty-seven samples from the Swartruggens and Star Group II kimberlite dyke swarms, emplaced through the Kaapvaal craton, have been analysed for their major and trace element and Sr, Nd and Hf isotope compositions. The samples are all MgO-rich (~12–35 wt%) with high Mg# (0.72–0.90) and Ni (~610–2700 ppm) contents. The kimberlites are strongly enriched in incompatible elements (Zr = 140–668 ppm; La = 124–300 ppm; Nb = 68–227 ppm; Ba = 1500–7000), and have high and variable chondrite normalised La/Yb ratios (Swartruggens = 94 ± 21; Star = 202 ± 36). ⁸⁷Sr/⁸⁶Sr (0.70718–0.71050) ratios are elevated, whereas εNd (−11.95 to −7.84) and ¹⁷⁶Hf/¹⁷⁷Hf ratios (0.282160–0.282564) are low. Inter- and intra-dyke compositional variation is significant, and there are systematic differences between the kimberlites found at the two localities. Intra-locality differences can largely be attributed to a combination of the effects of alteration, crustal contamination, macrocryst entrainment and phenocryst fractionation. There is some evidence for distinct parental magmas formed through variable and low degrees (0.5–2%) of partial melting, as illustrated by crossing rare earth element patterns. The Star kimberlites have derived from a less radiogenic source, with higher LREE enrichment than the Swartruggens kimberlites. Inferred primary magmas at each locality have high Mg# (~0.83), are Ni-rich (850–1220 ppm) and are strongly enriched in incompatible elements. Calculated mantle source compositions are strongly enriched in incompatible elements (La/Yb_n ~ 10–50), but refractory in terms of Mg# and Ni contents. Incompatible element ratios such as Ba/Nb (>13.5), La/Nb (> 1.1) and Ce/Pb (< 22) are unlike those characteristic of Group I kimberlites or ocean island basalts, but indistinguishable from calc-alkaline magmas. Taken together with extremely low εNd and εHf, these compositional characteristics are used to argue for derivation of these Group II kimberlite magmas from the deep subcontinental lithospheric mantle, metasomatised during the Proterozoic by calc-alkaline fluids/melts.     

The West Spitsbergen Fold Belt: The result of Late Cretaceous-Palaeocene Greenland-Svalbard convergence?

The West Spitsbergen Fold Belt, together with the Eurekan structures of northern Greenland and Ellesmere Island, are suggested to be the result of Late Cretaceous-Palaeocene intracontinental compressional tectonics. The Late Palaeozoic –Mesozoic rocks of western Spitsbergen are characterized by near-foreland deformation with ramp-flat, top-to-the east thrust trajectories, whereas structurally higher nappes involving Caledonian complexes are typified by more listric thrusts and mylonite zones. A minimum of 40 km of shortening is estimated for the northern part of the West Spitsbergen Fold Belt. The axial trends in the West Spitsbergen and the North Greenland Eurekan fold belts parallel the principal fault zones which accommodated the separation of Greenland and Svalbard after Chron 25/24. In northern Greenland, north directed Eurekan thrusts associated with mylonites and cleavage formation represent at least 10 km of shortening. Between 50 and 100 km of shortening is estimated for the markedly arcuate Eurekan Fold Belt of Ellesmere Island, but the principal tectonic transport is eastwards. Kinematic reconstructions suggest that Svalbard was linked to North America before the opening of the Eurasian Basin and Norwegian — Greenland Sea. In the Late Cretaceous — Palaeocene interval, the relative motion between Greenland and North America was convergent across the Greenland — Svalbard margin, giving rise to the West Spitsbergen Fold Belt and the Eurekan structures of North Greenland.     

Late Pleistocene and Holocene coastal palaeoeconomies: A reconsideration of the molluscan evidence from northern Spain

The worldwide increase in shell midden deposits on coastlines during the Holocene has been variously explained as the result of human population growth, economic intensification, changes in the visibility of midden deposits with changes in sea level, or climatic and environmental changes. Since coastlines are relatively unstable in geological and ecological terms, and since many archaeological sequences span periods of major climatic change, a critical issue is the ability to disentangle palaeoenvironmental from cultural and anthropogenic effects. We draw on a case study from the cave sequences of northern Spain to illustrate the problems and possibilities of palaeoeconomic and palaeoenvironmental interpretation, using studies of palaeogeographical context and analysis of abundance, taxonomic representation, ecological tolerances, size, growth structures, and other physical and chemical characteristics of the molluscs themselves. We demonstrate that the dominant, but by no means exclusive, factor in archaeologically visible long‐term changes in shell‐gathering behavior is environmental change rather than cultural change. © 2003 Wiley Periodicals, Inc.