ALBERT

Notes: Abstract The present study was undertaken to determine whether the various species of gobies that are found within the large Swan Estuary in south-western Australia are segregated within that system, and to attempt to determine the basis for any differences in their spatial distributions. The Swan Estuary comprises a long entrance channel (lower estuary), two wide basins (middle estuary) and the saline reaches of the tributary rivers (upper estuary). A total of 26232 gobies, representing seven species, was collected using a 3 mm-mesh seine net at 15 sites throughout this estuary on at least one occasion monthly over seven consecutive seasons between September 1983 and March 1985. Favonigobius lateralis and Pseudogobius olorum contributed 47.0 and 47.8%, respectively, to the total catch of gobies at all sites. The densities of each species at each site were used to determine the relative contribution of each species to the gobiid fauna at each of the sites in the lower, middle and upper estuary. Comparisons of these data with those published on the distribution and abundance of gobiid larvae confirmed that F. lateralis, which was found predominantly in the lower estuary, is a marine species that spawns in high salinities near the estuary mouth or in inshore coastal waters. In contrast, the life cycle of P. olorum and Papillogobius punctatus are typically completed within the saline reaches of the upper estuary, and that of Arenigobius bifrenatus within both this region and parts of the middle estuary where the substrate is particularly soft. Afurcagobius suppositus also spawns in this area, as well as in fresh water. Tridentiger trigonocephalus, represented by only eight individuals, is an introduced, marine species that was found mainly in the lower estuary. A single representative of the marine species Callogobius depressus was caught. The relatively low numbers of gobies caught in the middle estuary, where they contributed only about 3.5% to the total number of all gobies at all sites, may represent an aversion to the presence of rougher waters in the large basins. Circumstantial evidence suggests that the sandy substrate and consistently high salinities found in the lower estuary are preferred by F. lateralis, whereas the silty surface to the substrate and lower salinities of the upper estuary are preferred by Pseudogobius olorum. Densities of three of the four most abundant species were higher in either spring or summer than in winter, reflecting the influx of 0 + recruits, and possibly also the tendency for species in estuaries to congregate in the shallows during the warmer periods of the year. F. lateralis fed mainly on polychaetes and crustaceans, whereas P. olorum ingested predominantly algae, reflecting differences in mouth morphology and feeding behaviour, rather than the type of food available.

Notes: Abstract Samples of juveniles and adults of the goby Pseudogobius olorum were collected from seven sites in the shallows of the upper Swan Estuary, Western Australia, using a 3 mm-mesh seine net on one or two occasions in each month between September 1983 and April 1985. The mean gonadosomatic index of female fish rose from very low values in winter (June–August) to a sharp peak in mid-spring (October), reflecting the rapid maturation of ovaries over, this period. Ovaries with post-ovulatory follicles and ovaries that were undergoing degeneration were present, in November and December, but were then either rare or absent in those members of the corresponding cohort which survived into January and February. Female fish with advanced oocytes and mature ovaries were not found in December and January, but were present in February to April. The above trends exhibited by ovarian maturity indices, together with the appearance of larvae and small fish in both spring and autumn, demonstrate that P. olorum spawns in both spring and autumn and at best to only a limited extent in summer. Length-frequency and gonadal data show that the progeny of the spring-spawning group frequently spawn in the following autumn, when they are ∼ 5 mo old, and that those of the autumn-spawning group frequently spawn in the following spring, when they are ∼ 7 mo old. Some representatives of these two spawning groups survive through the winter and summer, respectively, to breed in a second season. Growth of the progeny of the spring-spawning group was relatively rapid between late spring and mid-autumn, whereas that of the autumn-spawning group was negligible during winter, but then inceased markedly in spring. It is proposed that the biannual spawning periods in each year by P. olorum in the Swan Estuary developed as a result of a rise in water temperature over the last few thousand years. Such a rise would have brought forward further into spring and extended later into autumn the periods when the water temperatures lie within the range (20 to 25°C) at which P. olorum typically spawns. However, mid-summer is now characterised by water temperatures 〉25°C, which are considered less conducive to reproductive success.

Notes: Abstract— This article describes the larval development and ontogenetic changes in diet of Nannatherina balstoni and constitutes the first description of flexion and postflexion larvae for the family Nannopercidae. Larvae were collected from pools in southwestern Australia. Larvae are elongate to moderately deep, lack head spines, have a moderate to large head and are moderately to heavily pigmented. Notochord flexion is complete by approximately 11 mm, i. e., longer than in members of the closely related Percichthyidae (≤ 9 mm). The sequence of fin completion, C, D2, A, D 1→P1→P2, also differs to that reported for percichthyids, but is the generalized condition within the percoids. The retention of a prominent notochord tip in postflexion larvae of N. balstoni is a characteristic that occurs in few teleosts. Nannatherina balstoni exhibits marked ontogenetic changes in diet. Larvae feed predominantly on cladocerans, copepods and dipteran larvae, whereas juveniles and adults ingest a large proportion of terrestrial fauna.

Notes: A magnetoresistive gradiometer to detect perpendicularly recorded transitions has been conceived. It utilizes two parallel magnetoresistive stripes with opposing sense/bias currents. The magnetoresistive elements mutually bias each other with the same polarity bias fields. The fields of a perpendicular transition centered between the two stripes increase the resistance of one stripe while decreasing that of the other, therefore providing maximum output signal using differential detection. The detector provides a Lorenztian-type readback waveform and rejection of common-mode noise. The experimental readback waveform exhibited a pulse width at half maximum of 0.7 μm for a head flying at 0.2 μm above the media surface.

Notes: The growth, age composition, reproductive biology and diet of Galaxiella nigrostriata in seasonal water bodies in south-western Australia are described and compared with G. munda and G. pusilla. Like the other two Galaxiella species, G. nigrostriata has a 1 year life cycle. The mean length attained by female G. nigrostriata at sexual maturity is approximately 37 mm, compared with about 47 and 28 mm for G. munda and G. pusilla, respectively. Like G. munda, G. nigrostriata is a multiple spawner. Although all three Galaxiella species breed mainly in winter and early spring, spawning occurs earlier in G. nigrostriata than in the other two species. An early production of offspring enables the young females and males of this species to reach approximately 78 and 88%, respectively, of their ultimate body length by early summer. Such a prolonged period of early and relatively rapid growth is advantageous to G. nigrostriata, since this species lives in water bodies that often dry up during the summer and early autumn and thus cannot grow during this period. The gonads start to undergo rapid development in autumn, when the pools begin to fill with water following the onset of the seasonal rains. All three Galaxielta species are carnivores. Galaxiella nigrostriata mainly takes prey from the water column and the water surface, G. pusilla focuses on prey in the water column and benthos, and G. munda feeds widely on prey on the water surface, throughout the water column and from the benthos. The prevalence of small prey, such as cladocera and calanoid copepods, is greater in the diets of G. nigrostriata and G. pusilla than in that of G. munda.

Notes: Nannatherina balstoni is found in a few acidic pools (pH 3.9–6.0) in the extreme south-western corner of Australia. Although many of these pools become dry during summer and early autumn, they are recolonized by fish from nearby pools that overflow during winter floods. N. balstoni spawns at the end of its first year of life, when, on average, the males and females have reached 60 and 63 mm t.l., respectively, and then usually die within the next few months. The largest fish, which was one of only three in its third year of life, measured 90 mm and weighed 7.3 g. The von Bertalanffy growth curve parameters for L0, K and t0 were 71.2 mm, 1.69 and – 0.078 for males and 82.6 mm, 1.31 and – 0.095 for females. Fecundity ranged from 550 to 1600. N. balstoni. spawns during the middle of winter, after heavy flooding and when water temperatures are at, or close to, their annual minima. This enables the larvae and young juveniles to capitalize on those aquatic organisms, especially Cladocera, which are very abundant amongst the flooded riparian vegetation that surrounds the pools in winter and spring. Hence, the fish grow rapidly and attain an appreciable size before summer, when the increases that occur in the densities of the larger carnivorous fish species, as a result of marked declines in water levels, increases the chances of predation. By spring, when most N. balstoni exceed 25 mm t.l., the diet changes markedly to one that consists almost exclusively of terrestrial fauna. In contrast, three of the six co-occurring native species of teleost feed on aquatic and terrestrial fauna throughout the year, while a further two feed only within the water column and the sixth feeds on benthic invertebrates. The pronounced shift in diet exhibited by N. balstoni as it increases in size, allied to dietary differences amongst the other six co-occurring species, reduces any potential for interspecific competition for food resources during the summer and autumn, when such resources are declining.

Notes: Protein, lipid, water and caloric contents of immature rainbow trout, relative to size of whole fish, growing at different rates were examined by use of allometric analysis (y = axb, Huxley, 1932). Fish grew at different rates as a result of differences in ration size (satiation, or 4–5% of dry body weight), temperature (7 and 12°C) and bGH (bovine growth hormone) administration. In fingerlings, protein, lipid and caloric contents tended to increase (v. body weight) as a percentage of body composition, whereas above fingerling size, protein decreased while lipid and caloric contents still increased. These trends occurred regardless of growth rate differences. The correlations between protein, lipid, caloric contents and body weight were high so reliable estimates of body components can be made from body weight for all experimental treatments. At satiation rations (7 and 12°C), there were no significant differences in protein content, but lipid and caloric contents were significantly higher in control fish. At low rations, protein and caloric contents were lower than those at satiation rations and lipid was lower than in the control group. On a dry weight basis, in uninjected fish at 12°C, ration size did not influence the percentage composition (protein and lipid) but the low ration group had lower energy values per unit of body dry weight. At low temperature (7°C satiation), fish had lower lipid and higher protein content (dry weight basis) than their controls (12°C satiation), thereby resembling bGH injected fish at satiation rations. Values of caloric content estimated from protein and lipid values by use of standard conversion factors differed sufficiently from caloric values directly determined by bomb calorimetry to suggest that caloric values of lipids may change during growth. The increase in body caloric content during growth apparently results mainly from an increase in the percentage of lipid. The similarity of body composition between different growth rate groups implied a tendency for conservation of relative proportions of components such that body composition can be approximated from body weight. Equations were also given to describe the relationship between water content and body constituents, and the relationship between condition factor (K) and both the body dry weight and lipid content.

Notes: The currents in the contact leads of a magnetoresistive (MR) head produce fields that influence the behavior of the underlying MR element. In the conventional lead configuration the current enters and leaves the MR element on the same side of the MR element. In the region where the conductor overlaps the MR element a field is produced that has a component that is along the easy axis of the MR element. The direction of this longitudinal field is in opposite directions on either side of the track and this destabilizes the MR element. Barkhausen noise results from the multidomain states that are produced. If instead the leads are configured to be on either side of the element the longitudinal fields are in the same direction and a single-domain state is stabilized. Results are presented that demonstrate the dependence of the hysteresis on the current. Kerr microscope measurements are shown that illustrate the behavior of the magnetization in the elements.

Notes: Isolated output pulse shapes are calculated for magnetoresistive gradiometer read heads having various geometric and magnetic parameters. The two-dimensional finite-element and reciprocity methods are used. The ferromagnetic shield has a big effect on the pulse shape, especially for closely spaces shields. High shield reluctance causes pulse broadening and large positive tails. Addition of a medium underlayer decreases the pulse undershoots and increases pulse amplitude. A reluctance model is given that explains most of the observed effects on pulse shapes and illustrates the importance of reluctance balance to achieve optimum pulse shape.

Notes: Biasing schemes for MR heads for use at high areal densities, O(108 bits/in.2), longitudinal recording, are reviewed. By use of the finite element analysis, a number of important design parameters are examined including the transfer function and the peak shift for each biasing scheme. We show that the roll-off peak shift and linearity characteristics are dependent on the type of bias scheme.