Effects of large organic material on channel form and fluvial processes

Stream channel development in forested areas is profoundly influenced by large organic debris (logs, limbs and rootwads greater than 10 cm in diameter) in the channels. In low gradient meandering streams large organic debris enters the channel through bank erosion, mass wasting, blowdown, and collapse of trees due to ice loading. In small streams large organic debris may locally influence channel morphology and sediment transport processes because the stream may not have the competency to redistribute the debris. In larger streams flowing water may move large organic debris, concentrating it into distinct accumulations (debris jams). Organic debris may greatly affect channel form and process by: increasing or decreasing stability of stream banks; influencing development of midchannel bars and short braided reaches; and facilitating, with other favourable circumstances, development of meander cutoffs. In steep gradient mountain streams organic debris may enter the channel by all the processes mentioned for low gradient streams. In addition, considerable debris may also enter the channel by way of debris avalanches or debris torrents. In small to intermediate size mountain streams with steep valley walls and little or no floodplain or flat valley floor, the effects of large organic debris on the fluvial processes and channel form may be very significant. Debris jams may locally accelerate or retard channel bed and bank erosion and/or deposition; create sites for significant sediment storage; and produce a stepped channel profile, herein referred to as ‘organic stepping’, which provides for variable channel morphology and flow conditions. The effect of live or dead trees anchored by rootwads into the stream bank may not only greatly retard bank erosion but also influence channel width and the development of small scour holes along the channel beneath tree roots. Once trees fall into the stream, their influence on the channel form and process may be quite different than when they were defending the banks, and, depending on the size of the debris, size of the stream, and many other factors, their effects range from insignificant to very important.     

黄河三角洲潮滩发育时空谱系

研究黄河三角洲潮滩发育的时空话系指出：在时间上，黄河三角洲潮滩系由不同时期河口滩发育而成，各段潮滩发育时间因素的差异在比较形态学上有清晰反映，在空间上，并存着处于不同发育阶段上的四种类型（阶段）。由此构成了黄河三角洲前沿所特有的湖滩形态时空体系。     

Gravel‐bed rivers: from particles to patterns

The papers in this special issue reflect several of the major themes and topics from the 7^th International Workshop on Gravel‐Bed Rivers. The papers focus primarily on aspects of bed material transport in gravel‐bed rivers and larger scale morpho‐dynamics. Research in gravel‐bed rivers is increasingly integrating processes over a wide range of temporal and spatial scales by combining field observation, lab experimentation, numerical modeling and theory testing in a range of river types, aided by new technological developments in particle tracking, computational modeling and high resolution spatial data. This is leading to greater understanding of the processes leading to distinctive morpho‐dynamics of river types and a more reliable basis for river management. Copyright © 2012 John Wiley & Sons, Ltd.     

The effect of a topographic high on the morphological stability of a two-inlet bay system

The cross-sectional stability of two tidal inlets connecting the same back-barrier lagoon to the ocean is investigated. The condition for equilibrium is the cross-sectional area tidal prism relationship. In an earlier study [Van de Kreeke, J., 1990. Can multiple inlets be stable? Estuarine, Coastal and Shelf Science 30: 261–273.], using the same equilibrium condition, it was concluded that where two inlets connect the same basin to the ocean ultimately one inlet will close. One of the major assumptions in that study was that the water level in the basin fluctuated uniformly. In hindsight this assumption might be too restrictive. For example, in the Wadden Sea the back barrier lagoon consists of a series of basins, rather than one single basin, separated by topographic highs. These topographic highs limit but do not exclude the exchange of water between the sub-basins. For this reason in the present study, a topographic high in the form of a weir was added, separating the back-barrier lagoon in two sub-basins. The water level in the sub-basins, rather than in the back-barrier as a whole, is assumed to fluctuate uniformly. For this schematization the hydrodynamic equations are solved using a finite difference method. The results, together with the equilibrium condition, yield the equilibrium flow curve for each of the inlets. The intersections of the two equilibrium flow curves represent combinations of cross-sectional areas for which both inlets are in equilibrium. The stability of the equilibriums was investigated using a non-linear stability analysis resulting in a flow diagram. Calculations were carried out for different inlet and weir characteristics. Sinussoidal tides were the same for both inlets. The results show that for relatively large wetted cross-sectional areas over the topographic high, approaching the situation of a single basin, there are no combinations of inlet cross-sectional areas for which both inlets are in a stable equilibrium. This supports the conclusion in the earlier study. For relatively small wetted cross-sectional areas over the topographic high there is one set of stable equilibriums. In that case the two-inlet bay system approaches that of two single-inlet bay systems.     

Evidence for discrete subpopulations of sea perch (Helicolenus ercoides) across four fjords in Fiordland,New Zealand

In coastal populations of invertebrates and fishes, the distribution of discrete subpopulations is influenced by adult and larval dispersal, as well as by the effects of habitat heterogeneity on site fidelity or connectivity. Here, we examine evidence for spatial structure of sea perch, Helicolenus percoides, populations among four fjords in the Fiordland region of southwestern New Zealand. We examine patterns in adult morphology, length-at-age, δ¹³C and δ¹⁵N of muscle tissue, and trace elemental composition of whole otoliths as proxies for population isolation among the four inner fjord regions. A multivariate analysis of morphometrics reveals significant differences among populations from each of the four sites, suggesting existence of four distinct subpopulations. These patterns are consistent with observed differences in δ¹³C and δ¹⁵N, and length-at-age estimates among the four subpopulations. Differences in whole otolith concentrations of Sr, Ba, Mg and Li, and high classification scores based on the whole otolith elemental fingerprint are also consistent with significant subdivision among areas. Patterns across all four markers are consistent with discrete subpopulation structure of adult sea perch among the four study sites. These data indicate that the newly implemented network of marine protected areas in Fiordland is likely to contain discrete populations of sea perch.     

Characterisation of Soot Emitted by Domestic Heating,Aircraft and Cars Using Diesel or Biodiesel

The characterisation of aggregates, like soot, firstly requires the determination of the size distribution of the primary particles. The primary particle size of combustion generated aggregates depends upon the combustion environment and the formation conditions, such as temperature, pressure and fuel-to-air ratio, among others. Since the combustion characteristics are different in the different types of burners, the characterisation of primary particles may offer the possibility to distinguish soot from different sources. In this paper, we present the signature of the primary particles and the aggregates of soot emitted by cars using diesel or biodiesel, by domestic heating, and by aircraft exhausts, which can be considered as the major sources as derived from measurements on transmission electron micrographs. The size distributions of all aggregates types with different aerodynamic diameter were log-normal and quasi-monodisperse. The size distribution of the primary particles for soot emitted by different sources showed minor differences. However, a comparison between the diameter of the primary particles and those obtained using a standard method for carbon black revealed discrepancies. The median diameter of the primary particles was combined with the median number of primary particles in an aggregate to calculate the relative particle surface area available for adsorption. In a similar way, the relative specific surface area was determined. The surface area was measured using the Brunauer-Emmett-Teller (B.E.T.) nitrogen adsorption method and the relative surface area available for adsorption was calculated.     

Interannual variability in the biochemical composition of newly hatched larvae of the spider crab Maja brachydactyla (Decapoda,Majidae)

The spider crab Maja brachydactyla is an important commercial species in Europe and supports intensive fisheries in the NE Atlantic. A field survey was performed to assess long‐term and consecutive interannual (2005–2010) variation of the biochemical composition of newly hatched larvae of M. brachydactyla. Larval biochemical profiles differed significantly among years, with pronounced differences being recorded in 2010. Differences among batches of newly hatched larvae were mainly explained by the contribution of triacylglycerols and, to a lesser degree, by protein and lipid content. The use of different nutrition indices is discussed. The biochemical composition of newly hatched larvae from M. brachydactyla was highly variable, even though surveyed broodstock was obtained from the same local population and was always sampled during the same season. The unpredictable biochemical profiles of newly hatched larvae may condition their survival and recruitment. This largely overlooked aspect of larval variability should be considered in future fisheries management strategies and captive production of marine organisms that still rely on wild seeds.     

Burrowing and burying by the crab Macrophthalmus hirtipes

Macrophthalmus hirtipes (Jacquinot, 1853) excavates burrows under water in soft, muddy sand that remains waterlogged at low tide. The crabs are immersed for at least 4 h in every tide. The burrows are usually single, blind‐ending, slightly curved passages; their openings do not appear to be deliberately closed by the crabs. Excavation is effected by using one set of walking legs as a scoop while the other set provides sideways traction.

Burrow openings are readily obscured by water movement, so that apparent burrow density does not give a true indication of the number of crabs in an area, but only indicates how many have been active recently; the true density may be found by sieving.

The burrowing activity of M. hirtipes is compared with that of other ocypodid crabs, and the functions of burrows are discussed. A distinction is made between excavating a burrow and rapid burying, because the two behaviours are very different, and must involve different adaptations and selection pressures.