Movement of Sub-Adult Striped Bass (Morone saxatilis) within an Estuarine Ecosystem Is there a spatial *Undergraduate Marine Biology, Sacramento City College 3845 Freeport Blvd. Sacramento, CA 95822-1386 † Rutgers University Marine Field Station, Institute of Marine and Coastal Sciences, 132 c/o 800 Great Bay Blvd. Tuckerton, NJ 08087 RESULTS ABSTRACT Hydrophone separation in adult and sub-adult striped bass populations ? Paul Clerkin*, Thomas Grothues†, and Kenneth Able† Big Fish 127 Small Fish 132 Small Fish 141 Small Fish 143 Small Fish 148 / 06 /17 07 / 06 /12 07 / 06 /07 07 / 06 /02 07 / 06 /27 06 / 06 /22 06 / 06 /17 06 / 06 /12 06 Fig. 1 Striped Bass (Morone saxatilis) Big Fish 59 / 06 /07 06 There was minimal movement of the tagged sub-adult striped bass. After release, subadults were most frequently detected in an upstream location of the estuary. Tagged adult striped bass also moved very little after release, residing primarily an open water bay portion of the estuary. Figures 8 and 9 shows this age segregation of the adult and sub-adult populations. This spatial separation of the two populations shows no clear preference for either water temperature or salinity (Fig. 10). Water temperature data indicate no age related preference. Salinity data exhibit adult and sub-adult clusters, but with no discernible pattern. There seemed to be no similarity in adult and sub-adults striped bass’s movements. The sub-adults were found farther up stream while the adults were more often found out in the bay (Fig. 11) We compared the movements of sub-adult striped bass, Morone saxatilis with those of adults in the Mullica River-Great Bay estuary in southern New Jersey. We used ultrasonic telemetry, both mobile and fixed listening stations to track fish tagged with acoustic transmitters. The movement of sub-adult bass were not similar to that of adults. Sub-adults occupied different areas of the Mullica River-Great Bay estuary from adults. Movement was sporadic but limited. Occupied areas were similar in both temperature and salinity, differing only in location, suggesting that segregation is based on factors not addressed in this study 8 7 6 5 4 3 2 1 0 Date Fig. 9 Time vs. hydrophone graph showing which stationary hydrophone the fish were at DISCUSSION The striped bass is keystone species in the Mullica River-Great Bay estuary (Fig. 1). Although they are not commercially harvested in New Jersey, the mid-Atlantic striped bass commercial catch has shown vulnerability to the mismanagement of spawning and nursery habitats. Recreational fishing for striped bass impacts local economies through the sale of fishing tackle and equipment, boat rentals, and motel and restaurant revenues. As an important striped bass spawning and nursery habit, the coastal rivers of New Jersey make a significant contribution to the mid-Atlantic striped bass stock. A considerable research interest in this species has focused on describing the movements of adult striped bass within an estuarine study area (Tupper & Able 2000) . Consequently, there is a large amount of data available for comparative analysis. Young striped bass are frequently observed in shallow, close-to-shore locations (Ng, 2006). To examine the possibility and cause of age-segregated movements, we used a system of stationary wireless hydrophones located strategically throughout the Mullica River-Great Bay estuary as well as mobile hydrophones to track the movements of acoustically tagged fish (Grothues et al. 2005) (Fig. 2). The spatial separation by age with this species seems unrelated to water temperature or salinity. Of examined environmental factors, geography (i.e., river vs. bay) appears to be the most important factor related to age segregation. This suggests a behavioral, rather than physiological explanation of the age separation, in which older, larger fish exclude, smaller, younger fish from prime feeding habitats. Such competitive exclusion based on dominance of prime territory by adults would effectively separate the species into two habitat utilization patterns based on age. Given that the diet of younger bass differs from that of adults and that only after two years are striped bass considered fully piscivoroius, spatial separations could have diet related variable as well. Further investigation is warranted. Fig. 2 Stationary and mobile hydrophones 35 30 Surface Temperature INTRODUCTION over time Big Fish 59 Big Fish 61 Big Fish 102 Small Fish 132 Small Fish 134 Small Fish 141 Small Fish 143 Small Fish 148 Big Fish 175 25 20 15 10 5 0 0 10 20 30 40 Surface Salinity B Fig. 10 Temperature vs. salinity graph, showing the environment in which the fish were found METHODS Fig. 3 Acoustic transmitter, measuring 11X5mm A Tagging: We caught six sub-adult striped bass by hook and line. Each fish was placed in a tank containing the anesthetic aminobenzoic acid ethyl ether. We surgically implanted an ultrasonic transmitter (Fig. 3) into the peritoneal cavity of each fish and closed the incision with three sutures (Fig. 4). An injection of oxytetracycline (Liquamycin) was administered into the dorsal musculature to guard against latent infection. The fish were marked with external tags to alert anglers of their status and then released (Fig. 5). Fig. 6 A portable hydrophone (A ) coupled with Tracking: We tracked the fine scale movements an SRX-400 receiver/processor (B) was used from a boat to track the fine scale movements of tagged fish from a boat using a portable of hydrophone at pre-set points. For this, we sub-adult striped bass. employed a baffled hydrophone coupled with an SRX-400 receiver/processor (Fig. 6). Contacts were recorded and used to map the locations of individuals. This data was compared to previously collected data for adult striped bass. Our mobile data complements that collected from an array of fixed hydrophones used for examining coarse-scale movements in serial fashion ( Fig. 7). REFFERENCES Grothues, T.M., K.W. Able, J. McDonnell and M.M. Sisak. “An Estuarine Observatory for Real-Time Telemetry of Migrant Macrofauna: Design, Performance and Constraints”. Limnology and Oceanography Methods 3: 275-289, 2005 Fig. 4 Implanting a transmitter into an B A anesthetized fish. A) making a incision using a sterilized surgical scalpel. B) suturing closed incision after implantation Ng, C.L.H. “Habitat Utilization and Movement Patterns of Adult Striped Bass, Morone Saxatilis, in a Aouthern New Jerest Estuary Using Acoustic Telemetry”. A Masters thesis. Fig. 11 Locations where large fish (blue dots) and small fish (red Fig. 8 Time vs. hydrophone dots) were detected by portable hydrophones. locations of the points routinely checked by portable hydrophone (inset). vs. number of contacts Fig. 7 Stationary telemetric infrastructure in the Mullica RiverFig. 5 Release of acoustically tagged subadult striped bass. Tupper, M., and K.W. Able “Movement and Food Habits of Striped Bass”. Marines Biology, 137, 1049-1057, 2000 Great Bay estuary. Acknowledgments. I want to thank Clare Ng, Jay Turnure and Paige Roberts for generously sharing their expertise on fish tracking, fellow novice trackers Gregory Henkes and Margaret Malone for always lending a helping hand when needed, and many others at the Rutgers Marine Field Station for all the kind assistance they have given this project.