New records of Philometra spp. (Nematoda: Philometridae) from marine perciform fishes off Florida, USA, including descriptions of two new species.

Recent examinations of marine perciform fishes from off the Florida coast in the Gulf of Mexico and Straits of Florida, USA, revealed the presence of the following six species of Philometra Costa, 1845 (Nematoda: Philometridae): P. haemulontis sp. n. (males and females) from the ovary of Haemulon plumierii (Lacepède) (type host) and H. aurolineatum Cuvier (both Haemulidae); Philometra synagridis Moravec, Bakenhaster et Fajer-Ávila, 2014 (males and females) from the ovary and testes of Lutjanus synagris (Linnaeus) (Lutjanidae); P. margolisi Moravec, Vidal-Martínez et Aguirre-Macedo, 1995 (male) from the ovary of Hyporthodus nigritus (Holbrook) (Serranidae) (new host record; probably a paradefinitive host); P. andersoni sp. n. (male) from the ovary of H. nigritus; Philometra sp. 1 (male) from the ovary of Rhomboplites aurorubens (Cuvier) (Lutjanidae); and Philometra sp. 2 (females) from the subcutaneous tissue of the anterior-most head sinuses of Hyporthodus niveatus (Valenciennes) (Serranidae). Specimens of species are described and illustrated based on light and (except for Philometra sp. 1) scanning electron microscopical examinations. Philometra haemulontis sp. n. differs from all congeners in the unique structure of the gubernaculum, whereas P. andersoni sp. n. can be differentiated from other gonad-infecting congeners parasitising the Serranidae by a combination of morphological features. Females of P. synagridis are described for the first time. Gravid females of Philometra sp. 2 are similar to those of P. morii Moravec, Bakenhaster et Fajer-Ávila, 2010, a subcutaneous parasite of Epinephelus morio (Valenciennes) (Serranidae) in the Gulf of Mexico.

Timing and locations of reef fish spawning off the southeastern United States.

Managed reef fish in the Atlantic Ocean of the southeastern United States (SEUS) support a multi-billion dollar industry. There is a broad interest in locating and protecting spawning fish from harvest, to enhance productivity and reduce the potential for overfishing. We assessed spatiotemporal cues for spawning for six species from four reef fish families, using data on individual spawning condition collected by over three decades of regional fishery-independent reef fish surveys, combined with a series of predictors derived from bathymetric features. We quantified the size of spawning areas used by reef fish across many years and identified several multispecies spawning locations. We quantitatively identified cues for peak spawning and generated predictive maps for Gray Triggerfish (Balistes capriscus), White Grunt (Haemulon plumierii), Red Snapper (Lutjanus campechanus), Vermilion Snapper (Rhomboplites aurorubens), Black Sea Bass (Centropristis striata), and Scamp (Mycteroperca phenax). For example, Red Snapper peak spawning was predicted in 24.7-29.0°C water prior to the new moon at locations with high curvature in the 24-30 m depth range off northeast Florida during June and July. External validation using scientific and fishery-dependent data collections strongly supported the predictive utility of our models. We identified locations where reconfiguration or expansion of existing marine protected areas would protect spawning reef fish. We recommend increased sampling off southern Florida (south of 27° N), during winter months, and in high-relief, high current habitats to improve our understanding of timing and location of reef fish spawning off the southeastern United States.

Effects of preservation methods of muscle tissue from upper-trophic level reef fishes on stable isotope values (δ (13)C and δ (15)N).

Research that uses stable isotope analysis often involves a delay between sample collection in the field and laboratory processing, therefore requiring preservation to prevent or reduce tissue degradation and associated isotopic compositions. Although there is a growing literature describing the effects of various preservation techniques, the results are often contextual, unpredictable and vary among taxa, suggesting the need to treat each species individually. We conducted a controlled experiment to test the effects of four preservation methods of muscle tissue from four species of upper trophic-level reef fish collected from the eastern Gulf of Mexico (Red Grouper Epinephelus morio, Gag Mycteroperca microlepis, Scamp Mycteroperca phenax, and Red Snapper Lutjanus campechanus). We used a paired design to measure the effects on isotopic values for carbon and nitrogen after storage using ice, 95% ethanol, and sodium chloride (table salt), against that in a liquid nitrogen control. Mean offsets for both δ (13)C and δ (15)N values from controls were lowest for samples preserved on ice, intermediate for those preserved with salt, and highest with ethanol. Within species, both salt and ethanol significantly enriched the δ (15)N values in nearly all comparisons. Ethanol also had strong effects on the δ (13)C values in all three groupers. Conversely, for samples preserved on ice, we did not detect a significant offset in either isotopic ratio for any of the focal species. Previous studies have addressed preservation-induced offsets in isotope values using a mass balance correction that accounts for changes in the isotope value to that in the C/N ratio. We tested the application of standard mass balance corrections for isotope values that were significantly affected by the preservation methods and found generally poor agreement between corrected and control values. The poor performance by the correction may have been due to preferential loss of lighter isotopes and corresponding low levels of mass loss with a substantial change in the isotope value of the sample. Regardless of mechanism, it was evident that accounting for offsets caused by different preservation methods was not possible using the standard correction. Caution is warranted when interpreting the results from specimens stored in either ethanol or salt, especially when using those from multiple preservation techniques. We suggest the use of ice as the preferred preservation technique for muscle tissue when conducting stable isotope analysis as it is widely available, inexpensive, easy to transport and did not impart a significant offset in measured isotopic values. Our results provide additional evidence that preservation effects on stable isotope analysis can be highly contextual, thus requiring their effects to be measured and understood for each species and isotopic ratio of interest before addressing research questions.