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Almaco jack Seriola rivoliana Findings from the NMFS Panama City Laboratory Trap & Camera Fishery-Independent Survey 24-214 D.A. DeVries, C.L. Gardner, P. Raley, and K. Overly SEDAR49-DW-15 29 April 21 This information is distributed solely for the purpose of pre-dissemination peer review. It does not represent and should not be construed to represent any agency determination or policy.

Please cite this document as: DeVries, D.A., C.L. Gardner, P. Raley, and K. Overly. 21. Almaco jack Seriola rivoliana Findings from the NMFS Panama City Laboratory Trap & Camera Fishery-Independent Survey 24-214. SEDAR49-DW-15. SEDAR, North Charleston, SC. 18 pp.

Almaco jack Seriola rivoliana Findings from the NMFS Panama City Laboratory Trap & Camera Fishery-Independent Survey 24-214 D.A. DeVries, C.L. Gardner, P. Raley, and K. Overly National Marine Fisheries Service Southeast Fisheries Science Center Panama City Laboratory Panama City, FL April 21 Panama City Laboratory Contribution 1-5 1

Survey history and overview In 22 the Panama City NMFS lab began development of a fishery-independent trap survey (PC survey) of natural reefs on the inner shelf of the eastern Gulf of Mexico off Panama City, FL, with the primary objective of establishing an age-based annual index of abundance for young (age -3), pre-recruit gag, scamp, and red grouper. Secondary objectives included examining regional catch, recruitment, demographic, and distribution patterns of other exploited reef fish species. The chevron trap is efficient at capturing a broad size range of several species of reef fish (Nelson et. al.1982, Collins 199), and has been used by the South Atlantic MARMAP program for over 2 yr (McGovern et. al. 1998). Initially the PC survey used the same trap configuration and soak time used by MARMAP (McGovern et. al. 1998), but an in-house study in 23 indicated that traps with a throat entrance area 5% smaller than that in the MARMAP traps were much more effective at meeting our objective of capturing sufficient numbers of all three species of grouper. Video data from our study and consultations with fishermen suggested that the presence of larger red grouper in a trap tended to deter other species from entering. Beginning in 24, the 5% trap throat size became the standard. That same year the survey was expanded east of Panama City to Apalachee Bay off the Big Bend region of Florida (Figure 1), an area separated from the shelf off Panama City by Cape San Blas - an established hydrographic and likely zoogeographic boundary (Zieman and Zieman 1989). Beginning in 25, the collection of visual (stationary video) data was added to the survey to provide insight on trap selectivity, more complete information on community structure, relative abundance estimates on species rarely or never caught in the trap, and additional, independent estimates of abundance on species typically caught in the traps. Video sampling was only done in Apalachee Bay that first year, but was expanded to the entire survey in 2. Also in 25, the target species list was expanded to include the other exploited reef fishes common in the survey area, i.e., red, vermilion, gray, and lane snapper; gray triggerfish, red porgy, white grunt, black seabass, and hogfish. From 25 through 28 each site was sampled with the camera array followed immediately by a single trap. Beginning in 29 trap effort was reduced ~5%, with one deployed at about every other video site, starting with the first site of the day. This was done to increase the number of video samples, and thereby the accuracy and precision of the video abundance estimates. Camera arrays are much less selective and provide abundance estimates for many more species than traps, and those estimates are usually much less biased (DeVries et al. 29). At each site, a CTD cast was made to collect temperature, salinity, oxygen, and turbidity profiles. Through 29 sampling was systematic because of a very limited sampling universe. In 21 the design was changed to 2 stage random after side scan sonar surveys that year yielded an order of magnitude increase in that universe (Figure 1). Five by five minute blocks known to contain reef sites, and proportionally allocated by region, sub-region, and depth (1-2, 2-3, 3+ m) to ensure uniform geographic and bathymetric coverage, are randomly chosen first. Then two known reef sites a minimum of 25 m apart within each selected block are randomly selected (Figure 2). Alternates are also selected for use when another boat is found to be fishing the site or no hard bottom can be found with sonar at that site. Depth coverage was ~8-3 m during 24-7, and then subsequently steadily expanded to ~8 52 m (Figure 3). Sampling effort has also increased since 24. Sample sizes were 59 in 24 (33 West: 2 East), 11 in '5 (24 W: 77 E), 114 in ' (25 W: 89 E), 8 in '7 (29 W: 57 E), 97 in '8 (31 W: E), 143 in '9 (47 W: 9 E), in '1 (53 W: 19 E), 18 in '11 (5 W: 115 E), 178 in ' (1 W: 117 E), 1 in 213 (71 W: 41 E), and 184 in 214 (113E: 71 W). Nine sites in 24 and 23 in 25 were sampled twice; thereafter each site was only sampled once in a given year. All sampling 2

occurred between May and October (with the exception of four sites in November, 213), but primarily during June through August (Figure 4). Sampling east of Cape San Blas in 213 was greatly reduced (down ~%) and done later than normal (Oct. and Nov.) due to late receipt of funding, ship mechanical issues, and weather problems. Methods Sampling was conducted during daytime from 1 hr after sunrise until 1 hr before sunset. Chevron traps were freshly baited each set with 3 previously frozen Atlantic mackerel Scomber scombrus, and soaked for 1.5 hr. Traps were fished as close as possible to the exact location sampled by the camera array. All trap-caught fish were identified, counted and measured to maximum total and fork length (FL only for gray triggerfish and TL only for black seabass). Both sagittal otoliths were collected from 4-5 randomly subsampled specimens of all snappers (gray, lane, red, and vermilion), groupers (gag, red, and scamp), black seabass, red porgy, hogfish, white grunt, and gray triggerfish (first dorsal spine for the latter). Visual data were collected using a stationary camera array composed of 4 Hi 8 video cameras (25 only) or 4 high definition (HDEF) digital video cameras (2-8) mounted orthogonally 3 cm above the bottom of an aluminum frame. From 27 to 29, parallel lasers (1 mm spacing) mounted above and below each camera were used to estimate the sizes of fish which crossed the field of view perpendicular to the camera. In 29 and 21, one of the HDEF cameras was replaced with a stereo imaging system (SIS) consisting of two high resolution black and white still cameras mounted 8 cm apart, one digital video (mpeg) color camera, and a computer to automatically control these cameras as well as store the data. The SIS provides images from which fish measurements can be obtained with the Vision Measurement System (VMS) software. Beginning in 211, a second SIS facing 18º from the other was added, reducing the number of HDEFs to two; and both SIS's were also upgraded with HDEF, color mpeg cameras. In 2 the two HDEFs were replaced with hi-def GoPro cameras. The camera array was unbaited 25-28, but since 29 has been freshly baited each drop with one previously frozen Atlantic mackerel placed in a mesh bag near the center. Before stereo camera systems were used (prior to 29), soak time for the array was 3 min to allow sediment stirred up during camera deployment to dissipate and ensure tapes with an unoccluded view of at least 2 min duration (Gledhill and David 23). With the addition of stereo cameras in 29, soak time was increased to 45 min to allow sufficient time for the SIS to be settled on the bottom before starting its hard drive, and to insure the hard drive had time to shut down before retrieval. In mid-213, stereo cameras were upgraded with solid state hard drives, enabling soak time to be reduced back to 3 min. Prior to 29, tapes of the 4 HDEF cameras were scanned and the one with the best view of the habitat was analyzed in detail. If none was obviously better, one was randomly chosen. In 29 only the 3 HDEF video cameras were scanned and the one with the best view of the reef was analyzed. Starting in 21, all 4 cameras the HDEFs and the SIS MPEGs, which have virtually the same fields of view (4 vs 5º) were scanned, and again, the one with the best view of the habitat was analyzed. Beginning in 2, when a video from a GoPro camera was selected to be read, because they have a much larger field of view than the SIS MPEGs (2 vs 5º), predetermined, equal portions of each edge of the video monitor were covered so that only the central 5 of the field of view was visible. Twenty min of the tape were viewed, beginning when the cloud of sediment disturbed by the landing of the array has dissipated. All fish captured on videotape and identifiable to at least genus were counted. Data on habitat type and reef morphometrics were also recorded. If the quality of the MPEG video derived from the SIS was less 3

than desirable (a common problem), fish identifications were confirmed on the much higher quality and concurrent stereo still frames. The estimator of abundance was the maximum number of a given species in the field of view at any time during the 2 min analyzed (= min count; Gledhill and Ingram 24, or MaxN; Ellis and DeMartini 1995), and VMS measurements were taken from a still frame showing the min count of a given species (but not necessarily the same frame the actual min count came from) to eliminate the possibility of measuring the same fish more than once. Even for deployments where the SIS did not provide a good view of the reef habitat, the files were examined to obtain fish measurements using VMS, and again, those measurements were only taken from a still frame showing the min count of a given species. In contrast, when scaling lasers were used to obtain length data, there was no way to eliminate the possibility of double measuring a given fish, although this was probably not a serious problem, as usable laser hits were typically rare for any one sample. Because of the significant differences we observed in both species composition and abundance of many reef fishes east and west of Cape San Blas, and because of the Cape s known status as a hydrographic and likely zoogeographic boundary (Zieman and Zieman 1989), many of the results presented herein are shown separately for the two areas. Censored data sets were used in deriving the indices of relative abundance from video data. All video samples were screened, and those with no visible hard or live bottom and no visible species of fish strongly associated with hard bottom habitat, as well as samples where the view was obscured because of poor visibility, bad camera angle, video out of focus, etc., were censored (excluded) from calculations of relative abundance. In 214, 1 video samples from an area with an ongoing serious red tide bloom, and which showed no or virtually no evidence of living fish, were also censored. As a result of this screening, of the video samples from east of the Cape, only 41 of 41 in 25, 84 of 89 in 2, 48 of 57 in 27, 1 of in 28, 8 of 97 in 29, 97 of 19 in 21, 1 of 115, in 211, and 15 of 115 in 2, 38 of 39 in 213, and 13 of 113 in 214 met the reef and visibility criteria and were retained. In contrast, west of the Cape, 25 of 25 sites in 2, 24 of 29 in 27, 29 of 31 in 28, 44 of 47 in 29, 5 of 53 in 21, of 4 in 211, 53 of 59 in 2, 7 of 72 in 213, and 71 of 71 in 214 were retained for analyses. Results Since the Panama City lab reef fish video survey began in 25, almaco jacks Seriola rivoliana have consistently and relatively commonly been observed with stationary video gear across the inner and mid-west Florida shelf both east and west of Cape San Blas (Table 1, Fig. 5) (DeVries et al. 28, 29, 2). In contrast, almaco jacks have only been captured in the Panama City lab trap survey once out of 875 deployments from 24 through 215 (one individual in 214), so there are no trap results to present herein. Although almaco jacks have been frequently observed swimming with schools of greater amberjack S. dumerili (personal observation by D. DeVries and C. Gardner), our survey has found almost no evidence that this species forms monospecific schools; 71% of positive samples had min counts of one, 17% had two fish, and the highest count was 7 (2 collections composing only 3% of all positive sites) (Fig. ). Encounter rates: Almaco jacks were never encountered in video samples shallower than 15.3 m and in only 1 out of 34 samples from depths < 18.2 m (where 3% of all sampling occurred) (Fig. 5 and 7). Encounter rates increased noticeably at the 2 m depth interval, with proportion positives fluctuating between. and.9 to the depth limits of the survey (Fig. 7). Because of the almost complete absence of almaco jacks in our shallow water samples, data summaries are presented both for collections from all depths and for collections only from depths 18.2 m. 4

Almaco jacks were more commonly encountered west of Cape San Blas than east, even when data from <18.2 m depths were excluded. During 2-214 the mean annual proportion of positive video samples in depths 18.2 m was.11 (range.4 to.3) west of Cape San Blas and. (range.-.13) in the east (Table 1, Fig. 8); with data from all depths included, those proportion remained unchanged in the west (.11, range.4 to.29) but dropped 5% to.3 (range.-.5) in the east (Table 1, Fig. 8). Certainly some of the difference between regions was related to the much larger proportion of shallow (<2 m) sites sampled east of the Cape prior to 29 (Fig. 3), as exclusion of all sites <18.2 m from the analysis virtually eliminated those differences in 27 and 28. However, after 29, even with the addition of many deep sites in the east and the exclusion of all sites <18.2 m, the proportion of positive observations remained higher west of the Cape than east every year except 2, averaging.9 and.4, respectively, 21-214 (Fig. 8). The overall mean proportion of positive video samples for east and west combined, 2-214, was. for all depths and.9 for depths 18.2 m (Fig. 9). After the extension of sampling into deeper waters east of Cape San Blas starting in 29, the trends in proportion positives were basically identical whether sites from all depths were included or just those >18.1 m, although the latter averaged 22% higher (range 19-28%) (Fig. 9). Abundance trends: Along with higher encounter rates, relative abundance estimates of almaco jack were also higher west of the Cape than east every year except 2 when data from all depths were examined, and every year except 29 and 2 if only depths 18.2 m were included (Fig. 1). Using data from all depths, mean video min count for 2-214 was.17 (range.5-.5) west of the Cape and.5 (range.-.1) in the east. If only data from depths 18.2 m were included, mean min count for 2-214 west of the Cape was unchanged, i.e.,.17 (range.5-.5); but east of the Cape the mean increased to. (range.-.5), over twice the estimate of.5 when all depths were included. As with proportion positives, the differences between east and west narrowed greatly in 2 and basically disappeared in 27 and 28 when the large number of shallow sites <18.2 m were excluded (Fig. 1). Excluding depths <18.2 m brought the mean difference between east and west of the Cape during 2-28 down an order of magnitude - from 428% (range 275-717) to 47% (range 4-113). Relative abundance of almaco jack on the northern West Florida Shelf increased sharply in 28, suggesting the recruitment of a new, strong year class, but it then dropped back to a much lower level in 29 and stayed at that level through 211 (Fig. 11). Relative abundance increased moderately in 2, remained level in 213, then fell in 214 to levels only slightly higher than those observed from 29 through 211 (Fig. 11). The similar trends in relative abundance east and west of the Cape, especially the very similar sharp rise in 28, suggests that the almaco jacks in these two regions belong to same stock. Since 29, the trends in the overall combined east and west data set were identical whether all depths were included or only depths 18.2 m; and mean nominal min counts from the 18.2 m data set averaged only 22% larger than those from the all depths data set (Fig. 11). Size structure: Almaco jacks observed with stereo cameras during 29-214 ranged from 227 to 48 mm FL and averaged 372 mm FL (Std error = 1)(Fig. ). Mean sizes from stereo image measurements were slightly larger east of Cape San Blas than west 399 vs 349 mm FL, although sample sizes were small (n= east and n=13 west) and 95% confidence intervals overlapped considerably. There appeared to be very little relationship between size of almaco jack and depth (Fig. 13). No attempt was made to model the relationship because of the small sample size and the very unequal distribution of data points across the depth range. 5

Annual GIS plots of video min counts show the spatial and temporal distributions of almaco jack for 25 214 (Fig. 14), but small sample sizes make it difficult draw any detailed conclusions from them. Literature Cited DeVries, D.A, J.H. Brusher, C.L. Gardner, and G.R. Fitzhugh. 28. NMFS Panama City Laboratory trap & camera survey for reef fish. Annual Report of 27 results. Panama City Laboratory Contribution 8-14. 2 pp. DeVries, D.A., J. H. Brusher, C. L. Gardner, and G. R. Fitzhugh. 29. NMFS Panama City Laboratory trap and camera survey for reef fish. Annual report of 28 results. Panama City Laboratory, Contribution Series 9-1. 22 p. DeVries, D.A., C.L. Gardner, P. Raley, and W. Ingram. 2. NMFS Panama City Laboratorytrap and camera survey for reef fish. Annual report of 211 results. Panama City Laboratory Ellis, D.M., and DeMartini, E.E. 1995. Evaluation of a video camera technique for indexing abundances of juvenile pink snapper, Pristipomoides filamentosus, and other Hawaiian insular shelf fishes. Fish. Bull. 93(1): 7 441 77. Gledhill, C., and A. David. 23. Survey of fish assemblages and habitat within two marine protected areas on the West Florida shelf. NMFS, Southeast Fisheries Science Center. Report to the Gulf of Mexico Fishery Management Council. Gledhill, C. and W. Ingram. 24. SEAMAP Reef Fish survey of Offshore Banks. 14 p. plus appendices. NMFS, Southeast Fisheries Science Center, Mississippi Laboratories. SEDAR 7 DW 15. GMFMC. 21. October 21 report of the Reef Fish Stock Assessment Panel. Gulf of Mexico Fishery Management Council, Tampa, FL. 34 pp. LO, N. C. H., L.D. Jacobson, and J.L. Squire. 1992. Indices of relative abundance from fish spotter data based on delta-lognormal models. Can. J. Fish. Aquat. Sci. 49: 2515-152. McGovern, J. C., G.R. Sedberry and P.J. Harris. 1998. The status of reef fish stocks off the southeast United States, 1983-199. Gulf and Caribbean Fisheries Institute 5: 871-895. Mahmoudi, B. 25. State-Federal Cooperative Reef fish Research and Monitoring Initiative in the Eastern Gulf of Mexico. Workshop report. March 3-4 25, Florida Fish and Wildlife Research Institute, St. Petersburg, Florida. Zieman, J.C., and R.T. Zieman. 1989. The ecology of the seagrass meadows of the west coast of Florida: A community profile. Biological Report 85(7.25). U.S. Fish and Wildlife Service. 155 p.

Tables Table 1. Annual video survey sample sizes, proportion positive occurrences, mean nominal video min counts, and standard errors of almaco jack east and west of Cape San Blas, 2-214, for all depths (A) and for all depths 18 m (B). Estimates calculated using censored data sets (see Methods). A. All depths included Proportion positive Mean nominal min Total sites sampled occurrences count Standard error Year East West Total East West Total East West Total East West Total 2 84 24 18.2.29.8.3.292.93.2.95.31 27 47 24 71.2.8.4.21.83.42.21.58.24 28 28 88.3.14.7.133.5.25.118.289.2 29 8 38 1.4.5.5.44.53.47.25.37.21 21 97 5 147..1.3..14.48..4.22 211 99 58 157..7.3..8.32..45.17 2 15 53 158.5.4.4..57.7.81.42.5 213 34 94.3.13.1.29.2.138.29.74.49 214 9 72 18.4.1.7.42.111.71.21.42.22 Total 9 47 197.3.1.5.51.147.85.17.28.15 B. Depths <18.2 m excluded Proportion positive Mean nominal min Total sites sampled occurrences count Standard error Year East West Total East West Total East West Total East West Total 2 21 23 44.1.3.2.143.34.227.14.98.72 27 15 24 39.7.8.8.7.83.77.7.58.43 28 1 27 43.13.15.14.5.519.5.438.299.245 29 32 37 9..5..3.54.58.43.38.28 21 71 5 1..1.4..14.58..4.27 211 5 58 3..7.3..8.41..45.21 2 8 53 133..4.5.213.57.15.1.42. 213 17 77..13..59.2.19.59.74. 214 7 71 138..1.8..113.87.29.43.2 Total 384 43 787.4.1.7.93.149.1.3.28.21 7

Figures Figure 1. Locations of all natural reefs in the sampling universe of the Panama City NMFS reef fish video survey as of November 214. Total sites: 2985 115 west of and 188 east of Cape San Blas. Isobath labels are in meters. Figure 2. Sampling blocks (5 min lat. x 5 min. long.) of the Panama City reef fish survey as of 214. Isobath labels are in meters. 8

Frequency Frequency West East 214 5 1 15 2 25 3 35 4 45 5 213 5 1 15 2 25 3 35 4 45 5 2 211 5 1 15 2 25 3 35 4 45 5 21 29 5 1 15 2 25 3 35 4 45 5 28 27 5 1 15 2 25 3 35 4 45 5 2 25 5 1 15 2 25 3 35 4 45 5 Depth (m) Figure 3. Annual depth distribution of Panama City reef fish survey video sample sites east and west of Cape San Blas, 25-214. 35 3 25 2 15 1 5 5 7 8 9 1 11 Month Figure 4. Overall monthly distribution of Panama City reef fish survey video and trap samples (censored data sets only), 24-214. 9 Video n=118 Trap n=99

Frequency Figure 5. Distribution and relative abundance of almaco jack observed with stationary, high definition video or mpeg cameras (min counts) in the Panama City NMFS reef fish survey, 24-214. Sites sampled, but where no almaco jack were caught or observed, are indicated with an X. 45 3 27 18 9 Positive video samples only 2-214 1 2 3 4 5 7 8 Min Count Figure. Frequency distribution of non-zero min counts of almaco jack from Panama City reef fish video samples, 2-214. 1

Proportion positive Frequency 25 2 15 1 5 All sites Sites with almaco jacks Propor +.1.8..4.2 Proportion + 5 1 15 2 25 3 35 4 45 5 55 Depth (m) Figure 7. Depth distributions of all video (24-214) sample sites vs only sites positive for almaco jack; and overall proportions of positive almaco jack video samples, 24-214, by depth. Proportion positive Proportion positive.35.3.25 24 All depths.2.15 28 24 5 72.1 58 38 15 84 9.5 47 34 8 97 99 53 25 2 27 28 29 21 211 2 213 214 215.35.3.25 23 Depths >18.1 m Figure 8. Annual proportions of positive almaco jack video samples, 2-14, by area (east vs. west of Cape San Blas) based on samples from all depths (upper panel) and on samples only from depths 18.1 m (lower panel). Numbers within the plot are total (not just positive) sample sizes for each year. 25 2 27 28 29 21 211 2 213 214 215 Figure 9. Annual proportions of positive almaco jack video samples, 2-14, east + west of Cape San Blas, based on samples from all depths and on samples only from depths 18.2 m. Numbers within the plot are total (not just positive) sample sizes for each year. 11. East of Cape West of Cape East of Cape West of Cape.2.15 27 24 5 71.1 1 32 58 8 21.5 15 37 17 7 71 5 53 25 2 27 28 29 21 211 2 213 214 215.25.2.15.1.5. 44 18 71 39 43 88 9 1 All depths 3 1 147 157 133 158 Only depths >18.1 m 77 94 138 18

Frequency Mean min count ± SE Mean min count ± SE 1.8. 28 All depths East of Cape West of Cape 24.4 5.2 24 15 72 58 38 53 84 47 8 97 99 34 9 25 2 27 28 29 21 211 2 213 214 215 1.8 27 Only depths >18.1 m East of Cape. West of Cape 1 23.4 5 8.2 24 21 32 58 71 15 71 5 17 7 37 53 25 2 27 28 29 21 211 2 213 214 215 Figure 1. Mean annual nominal video min counts (MaxN) of almaco jack east and west of Cape San Blas, 2-214, based on samples from all depths and from only depths 18.1 m. Numbers within the plot are sample sizes for each year. Mean min count ± SE.8. 43 East + West of Cape 2-214 All depths Only depths >18.1 m.4 44 133 77.2 39 9 1 158 138 18 88 3 94 71 1 18 147 157 25 27 29 211 213 215 Figure 11. Mean annual nominal video min counts (MaxN) of almaco jack for regions combined, 2-214, based on samples from all depths and from only depths 18.1 m. Numbers within the plot are sample sizes for each year. 4 West of Cape San Blas n=13 East of Cape San Blas n= 2 2 225 25 275 3 325 35 375 4 425 45 475 5 Fork length (mm) Figure. Overall size distributions of all almaco jacks measured in stereo images, 29-214, by region.

Fork length (mm) 5 4 3 2 Stereo measurements 29-214 1 East of Cape San Blas West of Cape San Blas 2 25 3 35 4 45 5 55 Depth (m) Figure 13. Fork length vs. depth relationship of almaco jacks east and west of Cape San Blas observed with stereo cameras, 29-14. 13

Video 25 Video 2 Figure 14. Annual distribution and relative abundance of almaco jack observed with stationary, high definition video or mpeg cameras (min counts) in the Panama City NMFS reef fish survey, 25-2. Sites sampled where no almaco jack were caught or observed are indicated with an X. 14

Video 27 Video 28 Figure 14 cont. Annual distribution and relative abundance of almaco jack observed with stationary, high definition video or mpeg cameras (min counts) in the Panama City NMFS reef fish survey, 27-28. Sites sampled where no almaco jack were caught or observed are indicated with an X. 15

Video 29 Video 21 Figure 14 cont. Annual distribution and relative abundance of almaco jack observed with stationary, high definition video or mpeg cameras (min counts) in the Panama City NMFS reef fish survey, 29-21. Sites sampled where no almaco jack were caught or observed are indicated with an X. 1

Video 211 Video 2 Figure 14 cont. Annual distribution and relative abundance of almaco jack observed with stationary, high definition video or mpeg cameras (min counts) in the Panama City NMFS reef fish survey, 211-2. Sites sampled where no almaco jack were caught or observed are indicated with an X. 17

Video 213 Video 214 Figure 14 cont. Annual distribution and relative abundance of almaco jack observed with stationary, high definition video or mpeg cameras (min counts) in the Panama City NMFS reef fish survey, 213-214. Sites sampled where no almaco jack were caught or observed are indicated with an X. 18