Experimental determinations of factors affecting the sink rates of baited hooks to minimize seabird mortality in pelagic longline fisheries

• 1. An experiment was conducted in Australia's pelagic longline fishery to establish a scientific basis for the introduction of line weighting to reduce seabird mortality. The experiment examined the effects of different bait species (blue mackerel, yellow‐tail mackerel and squid), bait life status (dead or alive), weight of leaded swivels (60 g, 100 g and 160 g) and leader length (distance between leaded swivel and hooks: 2 m, 3 m and 4 m) on the sink rates of baited hooks from 0–6 m deep.
• 2. On average, live bait sank much more slowly than dead bait. The sink rates of individual live bait were highly variable: many were <2 m underwater 18 s after deployment, including some on the heaviest swivels, and some were <10 m deep after 120 s.
• 3. Within the dead bait group, all three swivel weights on 3 m and 4 m leaders sank at similar rates. Initial sink rates (e.g. 0–2 m) were 2–3 times slower than final rates (e.g. 4–6 m) for all combinations of swivel weight and leader length. The fastest initial and final sink rates were associated with heavy swivels placed close to hooks.
• 4. The results show that (a) compared with dead bait, live bait greatly increases the exposure of baited hooks to seabirds; (b) initial sink rates of dead bait are increased by placing leaded swivels close to hooks and final rates by increasing the weight of the swivels; (c) adding weight to long leaders makes little difference to sink rates; and (d) the small (incremental) changes to swivel weights and leader lengths typically preferred by industry will be difficult to detect at sea and unlikely to substantially reduce seabird mortality.
• 5. We suggest that experiments designed to reduce seabird mortality from that associated with 60 g swivels and ～3.5 m leaders (the preferred option by industry) should aim to expedite the initial sink rates as well as rates to deeper depths. This objective could be achieved by including branch lines with ≥120 g swivels ≤2 m in comparative assessments of the effectiveness of line weighting regimes in reducing seabird mortality. Copyright © 2010 John Wiley & Sons, Ltd.

     

The periderms of three North American conifers

Summary The anatomy of periderms in three North American conifers are described and compared. The phellems of balsam fir and eastern hemlock consist of tangential bands of thin-walled phellem (TnP) separated by one, or sometimes more, cell layers of thick-walled phellem (TkP). The phellem of white spruce contains tangential bands of TnP and TkP, as well as one to several cell layers of crystalliferous phellem (CP) abaxially adjacent to every TkP zone. The TkP, and to a lesser extent the TnP, are distinctive for each of the three conifers.The terminations of phellem growth cycles in fir and hemlock are delineated by thickened adaxial suberinic walls in the last-formed layer of TnP cells. In spruce, the adaxial suberinic walls of the last-formed layer of CP cells are thickened. TkP marks the geginning of phellem growth cycles in all three conifers.TkP cells are true suberized phellem cells, not phelloids.     

A comparison of the population genetics of Lethrinus miniatus and Lutjanus sebae from the east and west coasts of Australia: Evidence for panmixia and isolation

Lethrinus miniatus and Lutjanus sebae are important commercial and recreational species of reef fish. Within Australian waters the former species is less widespread than the latter and has a discontinuous distribution, whilst the latter is continuously distributed in tropical Australian waters. The demographic attributes of these species (e.g. long life span, low rates of natural mortality) make them vulnerable to over-exploitation. Consequently, conservative harvest strategies including no-take zones for these species have been adopted by fisheries management agencies to control exploitation. Information on the genetic stock structure of these species is important for developing specific management strategies. However, little is known about genetic stock structures within and between east and west Australian populations of these species. The current study used the mitochondrial genome hypervariable region 1 (HVR1) of the control region to examine variation between two sites from both the east and west Australian coasts for each species. HVR1 for L. sebae did not differ genetically either within or between coasts (F_st < 0.018, p > 0.15) at the sites studied, suggesting a panmictic population structure. Similarly, L. miniatus did not differ significantly between sites sampled within coast. However, the west coast HVR1 for L. miniatus east and west coast populations, were discrete (F_st of at least 0.92, p < 0.0001). The degree of genetic sub-division between east and west coast populations indicates that they should be managed as discrete stocks. Further, when considering both species, the lower genetic (both haplotype and nucleotide) diversity in three of the four sites on the west coast of Australia, indicates that this region is genetically impoverished and neutrality tests suggest that selection is responsible. Consequently, west Australian populations will be less resilient to perturbations (e.g. fishing, climate change) than east Australian populations, which have higher genetic diversity.     

Effects of soil bulk density on seminal and lateral roots of young maize plants (Zea mays L.)

It is well established that increasing soil bulk density (SBD) above some threshold value reduces plant root growth and thus may reduce water and nutrient acquisition. However, formation and elongation of maize seminal roots and first order lateral (FOL) roots in various soil layers under the influence of SBD has not been documented. Two studies were conducted on a loamy sand soil at SBD ranging from 1.25 g cm^–3 to 1.66 g cm^–3. Rhizotrons with a soil layer 7 mm thick were used and pre‐germinated plants were grown for 15 days. Over the range of SBD tested, the shoot growth was not influenced whereas total root length was reduced by 30 % with increasing SBD. Absolute growth rate of seminal roots was highest in the top soil layer and decreased with increasing distance from the surface. Increasing SBD amplified this effect by 20 % and 50 % for the top soil layer and lower soil layers, respectively. At the end of the experiment, total seminal roots attributed to approximately 15 % of the total plant root length. Increasing SBD reduced seminal root growth in the lowest soil layer only, whereas FOL root length decreased with SBD in all but the uppermost soil layer. For FOL, there was a positive interaction of SBD with distance from the soil surface. Both, increasing SBD and soil depth reduced root length by a reduction of number of FOL roots formed while the length of individual FOL roots was not influenced. Hence, increasing SBD may reduce spatial access to nutrients and water by (i) reducing seminal root development in deeper soil layers, aggravated by (ii) the reduction of the number of FOL roots that originate from these seminal roots.