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Determining the geographic range of widely dispersed or migratory marine organisms is notoriously difficult, often requiring considerable costs and typically extensive tagging or exploration programs. While these approaches are accurate and can reveal important information on the species, they are usually conducted on only a small number of individuals and can take years to produce relevant results, so alternative approaches may be preferable. The presence of latitudinal gradients in stable carbon isotope compositions of marine phytoplankton offers a means to quickly determine likely geographic population ranges of species that rely on productivity from these resources. Across sufficiently large spatial and temporal scales, the stable carbon isotopes of large coastal or pelagic marine species should reflect broad geographic patterns of resource use, and could be used to infer geographic ranges of marine populations. Using two methods, one based on a global mechanistic model and the other on targeted low-cost latitudinal sampling of fishes, we demonstrate and compare these stable isotope approaches to determine the core population geography of an apex predator, the great hammerhead (Sphyrna mokarran). Both methods indicated similar geographic ranges and suggested that S. mokarran recorded in south-eastern Australia are likely to be from more northern Australian waters. These approaches could be replicated in other areas where coastlines span predictable geographic gradients in isotope values and be used to determine the core population geography of highly mobile species to inform management decisions.

The longhorned pygmy devil ray Mobula eregoodoo (Cantor, 1849), formerly known as Mobula eregoodootenkee (Bleeker, 1859), is a small mobulid with a disc reaching a maximum width of 1.3 m, widely ranging in tropical and subtropical latitudes across the Indian Ocean, the Indo-Pacific region, and the western Pacific Ocean. A recently emerged opportunity to examine several (n = 47) M. eregoodoo specimens bycaught in bather protection gillnets off New South Wales, Australia, together with new information assembled from other areas of its range, now allows for a redescription of the species, which was incompletely described in the past because of a paucity of specimens. Based on the morphometric, morphological, ecological, and behavioural elements presented here, corroborated by recent genetic investigations, we argue that M. eregoodoo (Cantor, 1849) is a valid species, distinct from shorthorned pygmy devil ray Mobula kuhlii (Muller & Henle, 1841). These findings are contrary to a recent revision of Mobula, where it was assessed as a synonym of M. kuhlii. The accuracy of taxonomic assessments underpins the effectiveness of species conservation, particularly when direct exploitation or bycatch in various fisheries needs to be managed for sustainability. Failing to recognize that two similar-looking species are distinct, such as M. eregoodoo and M. kuhlii, creates uncertainties that could result in mismanagement and underestimating local and global threats of extinction.

Penaeid trawling is among the world's least selective fishing methods; a characteristic that has evoked spatial closures being implemented in some fisheries if certain bycatch limits are exceeded. For decades, considerable work has been done to develop modifications to penaeid trawls that reduce unwanted bycatches, with most focussed at the posterior section (i.e. codend). More recently, efforts have examined ways to prevent bycatch entry into trawls entirely—via modifications to anterior components. This study assessed the utility of proactively lowering the headlines of Australian penaeid trawls, using clips at the otter boards, to 68% and 54% of their conventional height, and demonstrated mean total bycatch reductions (by weight) of 69% and 79%, respectively, with no effects on the targeted Metapenaeus macleayi (Haswell). The results provide insights into the location and behaviour of various species in the water column preceding capture, and support a simple and easy method for regional fishers to use in situ to avoid excessive bycatch and associated fishing closures. More broadly, the data support ongoing efforts in other penaeid-trawl fisheries to reduce bycatches via similar, rapid adjustments to anterior components, depending on species-specific behaviours during capture.

Estimates of age-specific natural (m) and fishing (f)mortalities among economically important stocks are required to determine sustainable yields and, ultimately, facilitate effective resource management. Here we used hazard functions to estimate mortality rates for eastern sea garfish, Hyporhamphus australis—a pelagic species that forms the basis of an Australian commercial lampara-net fishery. Data describing annual (2004 to 2015) age frequencies (0–1 to 5–6 years), yield, effort (boat-days), and average weights at age were used to fit various stochastic models to estimate mortality rates by maximum likelihood. The model best supported by the data implied: (i) the escape of fish aged 0–1 years increased from approximately 90 to 97% as a result of a mandated increase in stretched mesh opening from 25 to 28 mm; (ii) full selectivity among older age groups; (iii) a constant M of 0.52±0.06 year−1; and (iv) a decline in F between 2004 and 2015. Recruitment and biomass were estimated to vary, but increased during the sampled period. The results reiterate the utility of hazard functions to estimate and partition mortality rates, and support traditional input controls designed to reduce both accounted and unaccounted F.

The natural mortality (M) and purse-seine catchability and selectivity were estimated for yellowtail scad, Trachurus novaezelandiae, Richardson, a small inshore pelagic species harvested off south-eastern Australia. Hazard functions were applied to two decades of data describing catches (mostly stable at a mean ± SE of 315 ± 14 t p.a.) and effort (declining from a maximum of 2,289 to 642 boat days between 1999/2000 and 2015/2016) and interdispersed (over 9 years) annual estimates of size at age (0+ to 18 years) to enable survival analysis. The data were best described by a model with eight parameters, including catchability (estimated at <0.1 × 10−7 boat/day), M (0.22/year) and variable age-specific selection up to 6 years with a 50% retention among 5-year-olds (larger than the estimated age at maturation). The low catchability implied very low fishing mortality by the purse-seine fleet. Ongoing monitoring and applied gear-based studies are required to validate purse-seine catchability and selectivity, but the data nevertheless imply T. novaezelandiae could incur additional fishing effort and, in doing so, alleviate pressure on other regional small pelagics.

Estimates of age-specific natural (m) and fishing (f)mortalities among economically important stocks are required to determine sustainable yields and, ultimately, facilitate effective resource management. Here we used hazard functions to estimate mortality rates for eastern sea garfish, Hyporhamphus australis—a pelagic species that forms the basis of an Australian commercial lampara-net fishery. Data describing annual (2004 to 2015) age frequencies (0–1 to 5–6 years), yield, effort (boat-days), and average weights at age were used to fit various stochastic models to estimate mortality rates by maximum likelihood. The model best supported by the data implied: (i) the escape of fish aged 0–1 years increased from approximately 90 to 97% as a result of a mandated increase in stretched mesh opening from 25 to 28 mm; (ii) full selectivity among older age groups; (iii) a constant

Deep hooking is one of the key causes of mortality among angled-and-released teleosts worldwide. We assessed the effects of natural baits and other variables on the frequency of deep hooking and postrelease mortality in two Australian native freshwater fishes that are classified as vulnerable or endangered: Golden Perch Macquaria ambigua and Freshwater Catfish Tandanus tandanus. Sixty-one angled Golden Perch were released and monitored in individual submersible cages at their capture location or were held in shore-based group tanks; of these fish, 97% were hooked with natural baits, 41% were deep hooked and had their lines cut, and 44% died. Of the Golden Perch that died, 70% were deep hooked, and hook location and two associated factors (hook removal and ease of handling) were identified as significant predictors of mortality. Mortality of Golden Perch was also significantly greater during the afternoon session on the first day of angling than during other sessions and days. In contrast, of the 98 Freshwater Catfish that were similarly angled with natural baits, only 9% ingested hooks and only 3% died, with no significant mortality factors identified. None of the control fish died. Interspecific differences in deep-hooking frequency are discussed in relation to the significant influences of time of day (both species), angler experience (Freshwater Catfish), and river reach (Golden Perch) and the likely differences in mouth morphology and feeding mechanisms. The results indicate that anglers should refrain from using natural baits when fishing for Golden Perch so as to minimize deep hooking and postrelease mortality, which will ultimately help conserve and manage these stocks. Received December 15, 2014; accepted April 10, 2015