This study investigated the contribution of shrimp stocks in supporting the production of valuable predator species. Fishery-independent data on white shrimp, brown shrimp, and selected fish species (spotted seatrout, red drum, and southern flounder) were collected from 1986 to 2014 by the Texas Parks and Wildlife Department, and converted to catch-per-unit effort (CPUE). Here, the associations between the CPUEs of fish species as predators and those of shrimp species as prey in each sampled bay and sampling season were analyzed using co-integration analysis and Partial Least Squares Regression (PLSR). Co-integration analysis revealed significant associations between 31 of 70 possible fish/shrimp pairings. The analysis also revealed discernible seasonal and spatial patterns. White shrimp in August and brown shrimp in May were associated with fish CPUEs in bays located along the lower coast of Texas, whereas white shrimp in November was more strongly associated with fish CPUEs in bays located on the upper coast. This suggests the possible influence of latitudinal environmental gradient. The results of the PLSR, on the other hand, were not conclusive. This may reflect the high statistical error rates inherent to the analysis of short non-stationary time series. Co-integration is a robust method when analyzing non-stationary time series, and a majority of time series in this study was non-stationary. Based on our co-integration results, we conclude that the CPUE data show significant associations between shrimp abundance and the three predator fish species in the tested regions.
Citation: Fujiwara M, Zhou C, Acres C, Martinez-Andrade F (2016) Interaction between Penaeid Shrimp and Fish Populations in the Gulf of Mexico: Importance of Shrimp as Forage Species. PLoS ONE 11(11): e0166479. https://doi.org/10.1371/journal.pone.0166479
Editor: Chih-hao Hsieh, National Taiwan University, TAIWAN
Received: July 12, 2016; Accepted: October 28, 2016; Published: November 10, 2016
Copyright: © 2016 Fujiwara et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Data Availability: All relevant data are within the paper and its Supporting Information files.
Funding: This work was supported by an Institutional Grant (NA14OAR4170102) to the Texas Sea Grant College Program from the National Sea Grant Office, National Oceanic and Atmospheric Administration, U.S. Department of Commerce.
Competing interests: The authors have declared that no competing interests exist.
The shrimp industry is the most valuable fishery in the Gulf of Mexico; it is worth $588 million USD and accounts for 65% (by weight) of the total US shrimp landings . However, the important ecological contribution of shrimp stocks in supporting the production of valuable predator species is underestimated. Recent stock assessment models [2, 3] estimated that approximately 62 billion brown shrimp (Farfantepenaeus aztecus) and 14 billion white shrimp (Litopenaeus setiferus) are recruited as sub-adults in the Gulf of Mexico each year. The pre-recruitment natural mortality rate (i.e., that of post-larval and juvenile shrimp) was estimated to be 23–61% when predation was included, but only 3% in the absence of predation . This suggests that a significant number of juveniles are preyed upon before becoming available to the fishery, and highlights the potential importance of shrimp as a forage species.
In fisheries, species are considered forage species when they play a role as necessary prey for larger predators, such as larger fish, marine mammals, and seabirds . The term “forage species” has meaning beyond something that is eaten by predators. Its depletion must have a detrimental effect on the predators, and the depletion of forage species due to fisheries is a serious ecological concern because they compete with the needs of these predators. Small- to medium-sized pelagic fishes, such as anchovy (Family Engraulidae), menhaden (Brevoortia spp.), and mackerel (Scomber spp.), are considered forage species. Shrimp have some characteristics in common with these pelagic species, including: relatively short life spans and high vulnerability to environmental factors, which can obscure the relationship between stock abundance and recruitment [6, 7]; and high, often localized abundances (pelagic fish form schools, while juvenile shrimp aggregate in coastal areas), which can make them more vulnerable to predation.
Major predators of juvenile penaeid shrimp in Galveston Bay, TX, include southern flounder (Paralichthys lethostigma), spotted seatrout (Cynoscion nebulosus), and red drum (Sciaenops ocellatus) . These species support important recreational and commercial fisheries throughout the Gulf of Mexico [8, 9], and are highly sought after by recreational anglers in Texas . The availability of different species of juvenile penaeid shrimp varies seasonally in near- and inshore areas, where high predation occurs. White shrimp are more abundant during late summer and fall , whereas brown shrimp are more abundant during the spring and early summer . Consistent with this, analyses of the stomach contents of red drum revealed large numbers of white shrimp in juvenile/adult fish during the fall, but large numbers of brown shrimp, along with menhaden, during spring [13–15]. Southern flounder [4, 16] and spotted seatrout [17, 18] are also known to feed extensively on penaeid shrimp.
As a part of a project aimed at evaluating the importance of penaeid shrimp as a forage species, we investigated the statistical association between time series (1986–2014) data on the catch-per-unit effort (CPUE) of shrimp (white shrimp and brown shrimp) and fish (spotted seatrout, red drum, and southern flounder). Both white shrimp and brown shrimp exhibit an annual life history and utilize coastal marshes and estuaries during their juvenile stages, which are preyed upon by the juvenile and young adult stages of the studied fishes. The data used in this study targeted these stages of shrimp and fishes, and samples were collected in the major bays along the Texas coast as a part of a long-term monitoring program that was independent of any fishery. As co-linearity and non-stationarity are frequent problems in statistical associations of time series data, we used partial least squares regression (PLSR)  and co-integration analyses , and compared the results.
Fishery-independent data were collected by the Coastal Fisheries Division of the Texas Parks and Wildlife Department as part of the Marine Resource Monitoring Program conducted in major coastal bays of Texas. In the present study, we analyzed data obtained from Galveston Bay, Matagorda Bay, San Antonio Bay, Aransas Bay, Corpus Christi Bay, and the upper Laguna Madre (Fig 1) from January 1986 to July 2014. The surveys used gill nets and trawls to capture fish and shrimp, respectively (S1 Table).
For fish, gill net sampling was conducted twice a year, for the 10 weeks following the first full week of April (spring sampling) and the 10 weeks following the first full week of September (fall sampling). A total of 45 gill nets were set in each bay system per season, with no less than three gill nets set each week. The gill nets covered the water column from the seafloor to 1.2 meters above the bottom, had a total length of 182.9 m, and were constructed of four continuous 45.7 m-long panels of stretched mesh monofilament webbing of 152 mm, 127 mm, 102 mm, and 76 mm in size. Nets were set perpendicular to the shore, with the smallest mesh (76 mm) nearest the shore; they were deployed around sunset and retrieved around sunrise each day. Organisms greater than 5 mm in total length were identified to the lowest taxonomic level . Data were converted to CPUE (number of individuals caught per hour). For the present study, we selected the CPUEs of spotted seatrout, red drum, and southern flounder, as these are three major targets of recreational fisheries in Texas and the Gulf of Mexico.
For shrimp, bay trawl surveys were conducted monthly. To ensure proper spatial representation, larger bays (Galveston, West Matagorda, San Antonio, Aransas, and Corpus Christi) were stratified into approximately equal-sized upper and lower areas. A total of 20 trawls were conducted in each bay system per month, and scheduled to ensure the temporal representation of samples within a month. The first set of samples was collected during the first half of the month, and the remaining samples were collected during the second half of the month. Sampling was conducted during daylight hours from 30 minutes before sunset to 30 minutes after sunset. The utilized otter trawls had 6.1-m openings and were made of 38-mm stretched nylon multifilament mesh. They were towed for 10 minutes at 3 mph in a semi-circular manner. As with the gill net sampling, captured organisms greater than 5 mm in total length were identified to the lowest taxonomic level . Brown shrimp and white shrimp data were converted to CPUEs (number of individuals caught per unit time).
For most locations and years, the seasonal peak of brown shrimp was May and those for white shrimp were August and November. Therefore, the CPUEs of shrimp species from those months were used for the analysis (Fig 2). The CPUEs of the three fish species during spring (Fig 3) were compared with the CPUEs of white shrimp in the fall and brown shrimp in the spring of the previous year, while the CPUEs of fish during fall (Fig 3) were compared with CPUEs of white shrimp in the fall and brown shrimp in the spring of the same year. A comparison of fish data in fall and shrimp data from the previous fall would have been another logical choice, but it was not included because it would have decreased the length of the fish data by one year, thereby reducing the power of the analysis. The data from each bay in each season were analyzed separately. All data were transformed by taking the square root to stabilize the variance.
CPUEs of brown shrimp in May (panels a, c, e, g, i, and k) and white shrimp (panels b, d, f, h, j, and l) in August (circle) and November (triangle). Locations: (a-b) Galveston Bay, (c-d) Matagorda Bay, (e-f) San Antonio Bay, (g-h) Aransas Bay, (i-j) Corpus Christi Bay, and (k-l) Upper Laguna Madre. The original CPUEs were transformed by taking the square root and then standardized by taking the Z-score.
Left column: spotted seatrout; middle column: red drum; right column: southern flounder. Circles indicate spring, and x indicate fall. Locations: (a-c) Galveston Bay, (d-f) Matagorda Bay, (f-i) San Antonio Bay, (j-l) Aransas Bay, (m-o) Corpus Christi Bay, and (p-r) Upper Laguna Madre. The original CPUEs were transformed by taking the square root and then standardized by taking the Z-score.
Partial Least Squares Regression (PLSR) Analysis
Associations between the CPUEs of each fish species and those of each shrimp species for each bay in each fish-sampling season were analyzed using PLSR. This analysis is similar to canonical correlation analysis except that the error term in the PLSR analysis is a univariate, so the analysis assumes the direction of dependency for the variables. As this study aimed to investigate the importance of shrimp as forage species for larger fish species, the fish time series were treated as dependent variables while the shrimp time series were treated as independent variables (Table 1). Similar to canonical correlation analysis, this strategy takes advantage of co-linearity among time series to find components of dependent and independent variables that are associated with one another. The data were standardized by taking z-scores, and then analyzed using the “plsregress.m” function in MATLAB . The significance of each association was determined using a one-at-a-time cross validation. When adding one or more independent components significantly improved the sum of the squared prediction error for the dependent component, we concluded that there was significant association between the dependent and independent variables.
Co-integration analysis  was used to assess the association between two non-stationary time series, which was seen in the majority of the studied time series. Whereas non-stationarity is known to cause spurious results in linear regression, PLSR, and related analyses, co-integration analysis takes advantage of non-stationarity and finds a linear combination of time series that is stationary. The time series involved in such a combination are considered to be co-integrated with one another. Therefore, while PLSR analysis is advantageous in detecting association at high frequency fluctuation when time series are stationary, co-integration analysis is advantageous in detecting association at low frequency fluctuation when time series are non-stationary. Co-integration analysis can be viewed as a type of factor analysis in which two or more time series that can eliminate a non-stationary pattern together are identified. Suppose two non-stationary time series and are analyzed. Co-integration finds coefficient β such that the linear combination of the two time series is stationary.
Biologically, co-integrated population time series can result when the populations are regulated together but are not necessarily at an equilibrium point (e.g., they could be gradually recovering from past reduced abundance or declining due to over-exploitation). Co-integration can find associations among time series without identifying the source of a non-stationary pattern; this is advantageous in population time series analysis because such a pattern could be produced by many potential processes. Determining the source of non-stationary patterns using short time series is often very difficult. The co-integration method circumvents this problem. A more detailed description of the application of this method in population ecology is described in .
Because the power of co-integration analysis is weak , we applied it to one shrimp time series and one fish time series when both of them were non-stationary. The analysis was done using the Engle-Granger co-integration test . An appropriate time lag for the residual regression for testing stationarity was chosen based on Akaike Information Criteria with a correction for finite data set (AICC). For example, for the time lag of two, stationarity is tested using the following equation: where a and b are coefficients and εt is an independently identically distributed Gaussian error term. The time series xt is considered stationary when a is not significantly different from 0. The stationarities of the original time series were tested by the Augmented Dickey-Fuller test using MATLAB function “adftest.m,” and the co-integration analysis was performed using MATLAB function “egcitest.m” .
Although co-integration analysis is a relatively new statistical method in population time series analysis, the method is well established in econometrics , and its application to population time series has been described . The approach is conceptually similar to minimum/maximum autocorrelation factor analysis, which seeks a weighted linear combination of time series (factor) that maximizes a lag-one autocorrelation . The factor, which has the smoothest pattern in the data, is interpreted as being produced by underlying population processes, and is thus analyzed further [25, 26]. However, such a pattern is found within dependent or independent variables without any information from the opposite variable. In contrast, co-integration finds the weighted linear combination of dependent and independent variables that removes a non-stationary pattern from the data. Populations exhibiting such time series are interpreted as being regulated together through external environmental factors and/or species interactions.
A total of 54 time series were analyzed (Figs 2 and 3). PLSR analysis was used to individually compare the six fish time series from each bay (three in each spring and fall) with two or three shrimp time series, for a total of 36 comparisons. The results revealed eight significant associations (Table 1), but there was no discernible pattern with respect to space or species.
An Augmented Dickey-Fuller test suggested that a large number of the time series were non-stationary, but the lag-one differences of the time series were stationary. Because we were interested in finding non-stationary times series that become stationary through their linear combination (i.e., co-integrated time series), we eliminated the stationary time series from further analysis. In total, we compared 70 pairs (out of 108 possible pairs) of shrimp and fish time series using the Engle-Granger co-integration test. Under all of the comparisons, AICC suggested the time lag of two for residual regression. Of them, 31 were significant (Table 2). Inspection of these results further suggested that both white shrimp in August and brown shrimp in May were included in the associations for bays located on the lower coast of Texas, whereas white shrimp in November was more frequently found in the associations for the upper coast bay systems. All three species of fish investigated in this study appear to be affected by shrimp in all of regions. For each of the three shrimp time series, the fall and spring fish time series that exhibited the lowest p-values were selected and plotted in Figs 4 and 5.
Panels show: (a) co-integrated time series from Upper Laguna Madre; (b) white shrimp in August (circle) and spotted seatrout in spring (X) CPUEs in Upper Laguna Madre; (c) co-integrated time series from Galveston Bay; (d) white shrimp in November (circle) and spotted seatrout in spring (X) CPUEs in Galveston Bay; (e) co-integrated time series from Upper Laguna Madre; and (f) brown shrimp in May (circle) and spotted seatrout in spring (X) CPUEs. CPUEs were transformed by taking the square root and then standardized by taking the Z-score. The co-integrated time series shown in the left panels are the weighted linear combination of the time series shown in the right panels.
The panels show: (a) co-integrated time series from Upper Laguna Madre; (b) white shrimp in August (circle) and red drum in fall (X) CPUEs in Upper Laguna Madre; (c) co-integrated time series from San Antonio Bay; (d) white shrimp in November (circle) and red drum in fall (X) CPUEs in San Antonio Bay; (e) co-integrated time series from Upper Laguna Madre; and (f) brown shrimp in May (circle) and red drum CPUEs in fall (X). CPUEs were transformed by taking the square root and then standardized by taking the Z-score. The co-integrated time series shown in the left panels are the weighted linear combinations of the time series shown in the right panels.
The p-values of pairwise comparisons are shown. Significant co-integration association (p ≤ 0.05) is indicated by bold and asterisk*. The lack of a p-value indicates that one or both original time series were stationary and no co-integration test was performed.
The objective of this study was to seek evidence supporting the importance of penaeid shrimp as a forage species in the Gulf of Mexico. We hypothesized that if the availability of two of the most abundant shrimp species in the region was vital for the sustainability of fish species, the fluctuations in prey and predator species abundance should have a statistical association. Although one should not conclude a trophic interaction based solely on a statistical association, we propose that such an association would support the existence of significant trophic interactions when combined with the knowledge that shrimp are commonly found in the stomachs of these fish species [13–17]. To this end, we tested for statistical associations between shrimp (brown and white) and three fish species (spotted seatrout, red drum, and southern flounder) in coastal bays of Texas using two statistical methods.
The results from our PLSR analysis suggested that there were some statistical associations between the shrimp and fish CPUEs, but we could find no discernible pattern with respect to space or species. Similar to linear regressions and associated analyses, the PLSR analysis is known to exhibit an inflated Type 1 error (false positive) when applied to non-stationary time series. As a large number of the time series in this study was non-stationary, the associations of 22% of the tested pairs (8 of 36 comparisons) could reflect such error. Conversely, time series data often suffer from large sampling errors, which can obscure the associations and increase Type 2 error (false negative). Therefore, we could not draw any conclusion based solely on the results from the PLSR analysis.
Unlike PLSR analysis, co-integration analysis is robust when used on non-stationary time series. Interestingly, our co-integration revealed that 31 of 70 pairs exhibited significant associations, and we could identify a discernible spatial pattern. Both white shrimp in August and brown shrimp in May were important in the bays of the south, whereas white shrimp in November was important in the bays of the north. This suggests that there may be a latitudinal influence. For example, temperature is known to influence the survival and growth of shrimp in the Gulf of Mexico [11, 12]. This was demonstrated with statistical modeling of field and laboratory experimental data  and field observation data , and laboratory experiments . Therefore, it is possible that the latitudinal influence may be associated with a temperature gradient. However, salinity is also known to influence the vital rates of shrimp in the Gulf of Mexico [28–31], and freshwater input is higher in the northern bays than southern bays. Therefore, a salinity gradient is another possible environmental factor affecting shrimp abundance. Further studies on the influence of environmental factors on shrimp abundance are needed to understand the latitudinal gradient.
As co-integration identifies associations by finding a linear combination of data that produces a stationary time series, an identified association will not come from a year-to-year (i.e., high frequency) fluctuation. Instead, the association comes from a slowly changing (i.e. low frequency) pattern. Many potential causes of the low frequency pattern exist. For example, change in shrimping effort , deterioration of environmental conditions due to development  or climate change , or improvement of conditions due to restoration of estuaries  are possible causes.
On the other hand, high frequency fluctuations in shrimp CPUEs are likely from environmental fluctuations because both brown shrimp and white shrimp in the Gulf of Mexico exhibit weak stock-recruitment relationships [7, 36] and their total allowable catch in the region has not fluctuated with a high frequency, suggesting a strong influence of environmental conditions on their recruitment. However, the high frequency fluctuations are not translated into correlated high-frequency fluctuations in fish CPUEs because fish populations often include multiple ages. This process effectively acts as a moving average process, which is a low-pass filter, and the associations at high frequencies probably become statistical insignificant. It is unlikely that changes in the annual catch quotas of recreational fishing removed the associations at high frequencies because they would have also removed the associations at low frequencies.
As a part of our co-integration analysis, we also fitted a vector autoregressive (VAR) model with co-integrated variables to the data to generate a vector-error corrected (VEC) model . The identification of any additional significant association would have suggested an association at a higher frequency. However, we found almost no further significant association. This result, which is consistent with those from our PLSR analysis, emphasized the lack of association among the time series with respect to a year-to-year (i.e., high frequency) fluctuation.
Behavioral differences between brown and white shrimp have been suggested to create differences in their vulnerability to potential predators. For example, brown shrimp were found to be more abundant in vegetated than non-vegetated areas, whereas white shrimp were less selective among habitat types . This led to the hypothesis that white shrimp could be more vulnerable to predation than brown shrimp. However, our results suggest that the abundances of both shrimp species affect those of all three fish species with a regional (latitudinal) difference in their importance. This may be associated with their spatiotemporal distribution. The abundance of white shrimp in November (the sum of CPUEs from all years) was highest in Galveston Bay (the northernmost bay) and lower toward the south, whereas the abundances of white shrimp in August and brown shrimp in May were highest in San Antonio Bay, which is located approximately in the middle of the six bays. We hypothesize that the availability of shrimp relative to other potential prey species determines their importance as prey.
Commercial and/or recreational fishing for these species has a measurable impact on their populations and corresponding roles as prey or predators. Management actions have been required in response to shifts in population trends. By the mid 90’s the commercial shrimp fishery in Texas was overcapitalized and experiencing an excessive fishing effort, in order to address this situation, the Texas Parks and Wildlife Department introduced a limited entry and buyback program, which ended the sale of new commercial shrimp fishing licenses and provided funds for the purchase of existing licenses . Through this program, over 65% of bay and bait licenses have been bought back and retired, resulting in a considerable reduction in shrimp fishing effort. While environmental variables also have an important role in shrimp recruitment, survival, and growth, past studies have shown that fishing effort alone accounts for 60 to 70% in shrimp catch variability . Therefore, the observed low frequency fluctuations in shrimp abundance may be a result of the management actions.
Management actions have also affected populations of red drum, spotted seatrout, and southern flounder. Some of these actions include gear restrictions, such as a gill net ban in place since 1980 that benefited most fish species, or a more recent gigging ban in November, in response to a declining trend in southern flounder catch rates and designed to reduce fishing effort during their annual migration to the Gulf. Other actions include special designations, such as gamefish for red drum and spotted seatrout, which effectively ended the commercial fishery for these two species. Stock enhancement is another management measure that benefited red drum and spotted seatrout with about 25 million red drum and spotted seatrout juveniles produced and released every year into bay systems along the Texas’ coast in order to supplement their natural populations . Finally, bag and size limits, adjusted through time depending on population trends, are also traditional management tools and applied to these species. Therefore, it is plausible that these independent management actions on the five species are obscuring or enhancing the statistical associations among the time series.
When the importance of a fishery stock is evaluated, the analysis often considers only the market value of the landed mass. However, our analysis supports the idea that penaeid shrimp in the Gulf of Mexico are also important as forage species for the three fish species that constitute an important resource for recreational fisheries in the region. These are the most sought after fish species in Texas, with spotted seatrout and red drum standing out as the two most frequently landed species in the coastal waters of Texas . Thus, our findings suggest that we have underestimated the ecological value of shrimp stocks in the Gulf of Mexico. Moreover, because most of the shrimp biomass is produced in marshes and coastal wetlands , our findings stress the importance of protecting ecological integrity of such habitats with the goal of increasing the productivity of shrimp and the valuable fish species they support.
Any statistical analyses have associated potential errors, and co-integration analysis is not an exception. For example, an Augmented Dickey-Fuller test may spuriously categorize stationary time series as non-stationary. Then, a subsequent Engle-Granger co-integration test will conclude the existence of co-integration spuriously. However, in our analysis, the visual inspection of the original time series used in an Engle-Granger co-integration test suggests that many of them appear non-stationary. For example, the right panels of Figs 4 and 5 show the original time series used in the co-integration tests with highest p-values; those time series can be compared with the time series in Figs 2 and 3, which include both stationary and non-stationary time series used in the PLSR analysis. The Engle-Granger co-integration test is also sensitive to the choice of time-lag included. In this analysis, we used AICC to determine the time-lag because AICC selects the best model based on available data. However, any spurious conclusions with AICC will also lead to spurious results in the Engle-Granger co-integration. These two particular problems occur because of a general problem in statistical analysis where overall analysis is done in multiple steps. Consequently, statistical power and significance level for an overall statistical analysis are not the same as the statistical power and significance level of the final statistical analysis step (i.e., the Engle Granger co-integration test). We suggest this is one of the areas that still require further refinement with the method in the future.
Here, by combining the results from PLSR and co-integration analysis, we conclude that the CPUE data suggest a significant association between shrimp and fish in the Gulf of Mexico. The abundances of shrimp and fish both exhibit low frequency patterns (i.e., non-stationary), and the association is found at this frequency. In contrast, year-to-year fluctuations do not necessarily show any significant association, likely because the responses of fish populations are not immediate (i.e., low inertia; ). This may have reduced the number of significant associations identified in our PLSR analysis. However, based on our results, we speculate that we could increase the number of significant associations identified in our PLSR analysis if we included an appropriate time lag and increased the length of the time series. Future research in this area could shed additional light on our conclusions.
S1 Table. Original data used in the analysis.
Catch per unit effort (CPUE) of fish data collected in fall, fish data collected in spring, white shrimp data collected in August, white shrimp data collected in November, and brown shrimp data collected in May.
We thank Amanda Stoner for preparing Fig 1 and associate editor and two anonymous reviewers for providing constructive comments.
- Conceptualization: MF CA CZ.
- Data curation: FMA.
- Formal analysis: MF CZ.
- Funding acquisition: MF.
- Investigation: MF CZ CA FMA.
- Methodology: MF CZ.
- Project administration: MF.
- Resources: FMA.
- Software: MF.
- Supervision: MF.
- Visualization: MF.
- Writing – original draft: MF CA.
- Writing – review & editing: MF CZ CA FMA.
- 1. National Marine Fisheries Service. Fisheries Economics of the United States, 2014. U.S. Dept. of Commerce, NOAA Tech. Memo, NMFS-F/SPO-163, 237p. 2016.
- 2. Hart RA. Stock Assessment of White Shrimp (Litopenaeus setiferus) in the U.S. Gulf of Mexico for 2011. NOAA Technical Memorandum NMFS-SEFSC-637, 36p. 2012.
- 3. Hart RA. Stock asessment of Brown Shrimp (Farfantepenaeus aztecus) in the U.S. Gulf of Mexico for 2011. NOAA Technical Memorandum NMFS-SEFSC-638, 37p. 2012.
- 4. Minello TJ, Zimmerman RJ, Martinez EX. Mortality of Young Brown Shrimp Penaeus aztecus in Estuarine Nurseries. Transactions of the American Fisheries Society. 1989;118(6):693–708.
- 5. Alder J, Campbell B, Karpouzi V, Kaschner K, Pauly D. Forage fish: From ecosystems to markets. Annual Review of Environment and Resources. 2008;33(1):153–66.
- 6. Haas HL, Lamon Iii EC, Rose KA, Shaw RF. Environmental and biological factors associated with the stage-specific abundance of brown shrimp (Penaeus aztecus) in Louisiana: Applying a new combination of statistical techniques to long-term monitoring data. Canadian Journal of Fisheries and Aquatic Sciences. 2001;58(11):2258–70.
- 7. Nance JM. Gulf of Mexico Shrimp Fishery Recruitment Overfishing Definition; Workshop 2. NOAA Technical Memorandum NMFS-SEFSC-323, 12p. 1993.
- 8. VanderKooy S. The Flounder Fishery of the Gulf of Mexico, United States: A Regional Management Plan. Gulf States Marine Fisheries Commission Publication 83, Ocean Springs, Mississippi. 2000.
- 9. VanderKooy S. The Spotted Seatrout Fishery of the Gulf of Mexico, United States: A Regional Management Plan. Gulf States Marine Fisheries Commission Publication 87, Ocean Springs, Mississippi. 2001.
- 10. Green LM, Campbell RP. Trends in Finfish Landings of Sport-Boat Anglers in Texas Marine Waters, May 1974 –May 2008. Texas Parks and Wildlife Department, Coastal Fisheries Division, Management Data Series No. 257, 634p. 2010.
- 11. Muncy RJ. Species Profiles: Life Histories and Environmental Requirements of Coastal Fishes and Invertebrates (Gulf of Mexico)—White Shrimp. U.S. Fish and Wildlife Services, Division of Biological Services, FWS/OBS-82/11.20. U.S. Army Corps of Engineers, TR EL 82–4, 19p. 1984.
- 12. Lassuy DR. Species Profiles: Life Histories and Environmental Requirements (Gulf of Mexico)—Brown Shrimp. U.S. Fish and Wildlife Services, Division of Biological Services, FWS/OBS-82/11. U.S. Army Corps of Engineers, TR EL 82–4, 15p. 1983.
- 13. Boothby RN, Avault JW. Food habits, length-weight relationship, and condition factor of red drum (Sciaenops ocellata) in Southeastern Louisiana. Transactions of the American Fisheries Society. 1971;100(2):290–&.
- 14. Overstreet RM, Heard RW. Food of the Red Drum, Sciaenops-Ocellata, from Mississippi Sound. Gulf Research Reports. 1978;6(2):131–5.
- 15. Scharf FS, Schlicht KK. Feeding habits of red drum (Sciaenops ocellatus) in Galveston Bay, Texas: Seasonal diet variation and predator-prey size relationships. Estuaries. 2000;23(1):128–39.
- 16. Stokes GM. Life history studies of southern flounder (Paralichthys lethostigma) and Gulf flounder (P. albigutta) in the Aransas Bay area of Texas: Texas Parks and Wildlife Department; 1977.
- 17. Minello TJ, Zimmerman RJ. Selection for Brown Shrimp, Penaeus-Aztecus, as Prey by the Spotted Seatrout, Cynoscion-Nebulosus. Contributions in Marine Science. 1984;27(Sep):159–67. pmid:WOS:A1984ACF6000010.
- 18. Simonsen KA, Cowan JH. Effects of an Inshore Artificial Reef on the Trophic Dynamics of Three Species of Estuarine Fish. Bulletin of Marine Science. 2013;89(3):657–76.
- 19. Garthwaite PH. An Interpretation of Partial Least-Squares. Journal of the American Statistical Association. 1994;89(425):122–7.
- 20. Engle RF, Granger CWJ. Cointegration and error correction—Representation, estimation, and testing. Econometrica. 1987;55(2):251–76.
- 21. Martinez-Andrade F. Marine Resource Monitoring Operations Manual. Texas Parks & Wildlife Department, Coastal Fisheries Division, Austin, Texas, 127p. 2015.
- 22. MATLAB. Ver. 8.5. The MathWorks, Inc., Natic, Masacchusetts, U.S.A. 2015.
- 23. Zhou C, Fujiwara M, Grant WE. Finding regulation among seemingly unregulated populations: a practical framework for analyzing multivariate population time series for their interactions. Environmental and Ecological Statistics. 2016;23(2):181–204.
- 24. Solow AR. Detecting change in the composition of a multispecies community. Biometrics. 1994;50(2):556–65. pmid:19405215
- 25. Fujiwara M. Identifying interactions among salmon populations from observed dynamics. Ecology. 2008;89(1):4–11. pmid:18376540
- 26. Fujiwara M, Mohr MS. Identifying environmental signals from population abundance data using multivariate time-series analysis. Oikos. 2009;118(11):1712–20.
- 27. Adamack AT, Stow CA, Mason DM, Rozas LP, Minello TJ. Predicting the effects of freshwater diversions on juvenile brown shrimp growth and production: a Bayesian-based approach. Marine Ecology Progress Series. 2012;444:155–73.
- 28. Zein-Eldin ZP, Aldrich DV. Growth and survival of postlarval Penaeus aztecus under controlled conditions of temperature and salinity. Biological Bulletin. 1965;129(1):199–216.
- 29. Rozas LP, Minello TJ. Variation in penaeid shrimp growth rates along an estuarine salinity gradient: implications for managing river diversions. Journal of Experimental Marine Biology and Ecology. 2011;397(2):196–207.
- 30. Saoud IP, Davis DA. Salinity tolerance of brown shrimpFarfantepenaeus aztecus as it relates to postlarval and juvenile survival, distribution, and growth in estuaries. Estuaries. 2003;26(4):970–4.
- 31. Rosas C, Ocampo L, Gaxiola G, Sánchez A, Soto LA. Effect of salinity on survival, growth, and oxygen consumption of postlarvae (PL10-PL21) of Litopenaeus setiferus. Journal of Crustacean Biology. 1999:244–51.
- 32. Hart RA, Nance JM. Three Decades of U.S. Gulf of Mexico White Shrimp, Litopenaeus setiferus, Commercial Catch Species. Marine Fisheries Review. 2014;75(4):43–7.
- 33. Rozas LP, Minello TJ, Zimmerman RJ, Caldwell P. Nekton populations, long-term wetland loss, and the effect of recent habitat restoration in Galveston Bay, Texas, USA. Marine Ecology Progress Series. 2007;344:119–30.
- 34. Zimmerman RJ, Minello TJ, Rozas LP. Salt marsh linkages to productivity of penaeid shrimps and blue crabs in the northern Gulf of Mexico. Concepts and controversies in tidal marsh ecology: Springer; 2002. p. 293–314.
- 35. Rozas LP, Minello TJ. Marsh terracing as a wetland restoration tool for creating fishery habitat. Wetlands. 2001;21(3):327–41. pmid:WOS:000171281800002
- 36. Klima EF, Baxter KN, Patella FJ. A Review of the Offshore Shrimp Fishery and the 1981 Texas Closure. Marine Fisheries Review. 1982;44(9–10):16–30. pmid:WOS:A1982PT44800003.
- 37. Minello TJ, Zimmerman RJ. Differential selection for vegetative structure between juvenile brown shrimp (Penaeus aztecus) and white shrimp (P. setiferus), and implications in predator-prey relationships. Estuarine Coastal and Shelf Science. 1985;20(6):707–16. http://dx.doi.org/10.1016/0272-7714(85)90027-7.
- 38. TPWD. The Texas shrimp fishery. A report to the Governor and 77th Legislature of Texas. Executive summary. Texas Parks and Wildlife Department. Austin, Texas. 2002.
- 39. TPWD. Texas Parks and Wildlife Department website, https://tpwd.texas.gov/fishing/sea-center-texas/marine-fish-hatchery, accessed September 26, 2016.
- 40. Zimmerman RJ, Minello TJ, Rozas LP. Salt marsh linkages to productivity of penaeid shrimps and blue crabs in the northern Gulf of Mexico. Concepts and Controversies in Tidal Marsh Ecology. 2000:293–314.
- 41. Murdoch WW. Population regulation and population inertia. Ecology. 1970;51(3):497–&.