RESOURCES

We don’t expect you to take our word for it when we make a recommendation for your pond.

The following studies and articles have helped our understanding of lake and pond management; we have organized them by topic so you can quickly find the information you need. For the sake of space on our website, we have posted just the abstracts of the studies, while for the shorter articles that are available online, we have posted the link. We hope this section will be helpful to you in growing giant bass and bluegill in your pond!

Habitat

  • Rold, Robert E. et. al. (1996). A Comparison of Cedar Trees and Fabricated Polypropylene Modules as Fish Attractors in a Strip Mine Impoundment. North American Journal of Fisheries Management, Vol. 16, 223-227, 08 Jan. 2011.

    Abstract: Two types of attractors, brush units of eastern red cedar Juniperus virginiana and fabricated polypropylene module attractors. were placed in a strip mine impoundment and evaluated for effectiveness in concentrating fish. Scuba diving was used to evaluate the attractors every 2 weeks from July to October. Fish that were 10 cm total length or larger were counted at all study locations and included bluegill Lepomis macrochirus, redbreast sunfish L. auritus. largemouth bass Micropter-us salmoides, green sunfish L. cyanellus, crappies Pomoxis spp., and channel catfish Ictalurus punctatus. Of the 623 fish observed during eight dives, brush attractors held 78% . module attractors 17%, and control areas 5%. Comparison of attractors by date and species revealed a tendency for them to attract more fish in July and August than in September and October.

  • Magnelia, Stephan J. et. al. Comparison of Plastic Pipe and Juniper Tree Fish Attractors in a Central Texas Reservoir. January 2008.

    Abstract: Fish attractors are commonly used by fisheries agencies to concentrate cover-seeking species. The objective of this study was to determine if an attractor fabricated with polyethylene pipe (plastic) attracted and concentrated as many largemouth bass (Micropterus salmoides) and sunfish (Lepomis sp.) as juniper tree (Juniperus ashei) attractors. Fish counts at each attractor type were made by scuba divers at five study sites in Canyon Reservoir, Texas. Overall, few fish were observed in the plastic attractors (mean = 3.4) compared to juniper tree attractors (mean = 30.3) (P < 0.05). Significantly greater numbers (P < 0.05) of adult and juvenile largemouth bass and bluegill (juvenile and adult) were concentrated in juniper attractors compared to plastic attractors. While 81% of the attractors deployed at the test sites were plastic, there was strong evidence (P < 0.05) that bluegill (adults and juveniles) and adult largemouth bass selected juniper attractors. Juvenile bluegill were the most abundant species and life stage observed (71% of the fish observed), which may have attracted foraging adult largemouth bass. Although fabricated plastic fish attractor designs are desirable because of their longevity, their effectiveness for attracting and concentrating target species should be evaluated prior to being used in large scale projects.

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  • Tugend, K.I., Allen, M.S. and Webb, M. (2002). Use of Artificial Habitat Structures in U.S. Lakes and Reservoirs: A Survey from the Southern Division AFS Reservoir Committee. Fisheries, 27: 22-27.

    Abstract: In 1999, the Southern Division American Fisheries Society Reservoir Committee conducted a survey to identify state agency goals, uses, and perceived effectiveness of artificial habitat structures in lakes and reservoirs. Of those states surveyed, 82% conducted some type of enhancement. In most states, 20% percent of water bodies received enhancement although respondents usually believed a larger portion of lakes and reservoirs (>40%) needed enhancement. Although several objectives were identified, most structures were placed to attract fish to increase angler catch rates. When asked to rate the effectiveness of structures on a scale of one (very satisfied) to five (very dissatisfied) with regards to agency objectives, most structures received a mediocre rating with mean values lying between two and three. Although abut 60% of states reported evaluation of structures, evaluations usually were testing for differences in fish abundance or angler catch rates between habitat structures and control areas. Few studies documented effects of structures on fish recruitment or population size. More studies are needed to assess effects of habitat structures on recruitment and abundance of sport fish in lakes and reservoirs. Readers are referred to an online habitat enhancement manual for more information on structures reported in this survey.

  • Allen, Micheal S. et. al. (2003). Largemouth Bass Abundance and Angler Catch Rates following a Habitat Enhancement Project at Lake Kissimmee, Florida. North American Journal of Fisheries Management 23(3):845-855, August 2003.

    Abstract: A habitat enhancement project was conducted at Lake Kissimmee, Florida, during1995–1996 to improve fish habitat and remove dense inshore vegetation caused by stabilized waterlevels. We evaluated abundance of age-1 (,250 mm total length [TL]) and adult (fish at least 356mm TL and all sizes of fish caught by anglers) largemouth bassMicropterus salmoidesbefore andafter the habitat enhancement. Mean electrofishing catch per hour (CPH) of age-1 largemouth bas-sincreased significantly after the 1995–1996 habitat enhancement, suggesting strong year-classesfor 2 years after the habitat enhancement (i.e., 1997–1998 year-classes). Growth of age-1 large-mouth bass also increased following habitat enhancement; mean total length of age-1 fish averaged143 mm before enhancement and 186 mm after enhance-ment. Catch curves conducted in 2001and 2002 corroborated historical electrofishing data indicating that the 1997 and 1998 year-classeswere abundant as adults compared with other year-classes in the age frequencies. Age-1 largemouth-bass electrofishing catch rates were not related to seasonal water levels or coverage of hydrillaHydrilla verticilla-ta. Despite the rapid growth rates and high abundance of the 1997 and 1998year-classes, neither electrofishing catch rates of largemouth bass at least 356 mm TL nor anglercatch rates of largemouth bass (fish/h, all sizes of fish, harvested or released; data from creelsurveys) differed significantly between preenhancement and postenhancement periods. Thus, wewere unable to detect a change in adult largemouth bass abundance or angler catch rates followingthe habitat enhancement. Fishing effort directed toward largemouth bass declined after enhance-ment for the winter period (No-vember–February) but did not differ significantly between preen-hancement and postenhancement periods for the summer (May–August) period. Benefits of muckremoval concurrent with lake drawdowns include increased recreational opportunities and improvedhabitat. However, our results indicate that fish population responses to drawdowns and muckremovals may vary and detecting effects on the adult largemouth bass populations can be difficult.Therefore, habitat enhancement efforts should focus on lakewide recreational benefits rather thanbenefits to a single preferred species (e.g., largemouth bass).

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Largemouth Bass

  • Sammons, Steven & Maceina, Michael. 2005. Population Size, Survival, and Growth of Largemouth Bass One Year After stocking in Four Ponds. Proceedings of the Southeastern Association of Fish and Wildlife Agencies, 59: 241-250.

    Abstract: Juvenile largemouth bass (Micropterus salmoides; approximately 50 mm total length) were stocked into four ponds (0.9 to 5.3 ha) at a rate of 248 fish ha –1 in late May 2003. Ponds were sampled the following spring to determine population characteristics. Largemouth bass survival ranged from 39% to 57% and appeared to be inversely related to pond size. Growth was rapid, with mean weight increasing from 1.8 g to 200–273 g in 300 days. Faster growing largemouth bass expressed greater relative weights. Catch rates of small (75 to 130 mm) bluegill (Lepomis macrochirus) were highly correlat-ed to pond size and bluegill may have reduced largemouth bass survival. Catch rates of large (130 to 150 mm total length) bluegills varied much less among ponds, but ponds with bluegill catch rates ≥100 fish/hour electrofishing were character-ized by greater largemouth bass relative weights. Bioenergetic models predicted that largemouth bass in these ponds were consuming food (primarily bluegill) at extremely high rates (P-values [proportion of maximum consumption] 0.98 to 1.04) in order to maintain the observed fast growth. Estimated bluegill consumption by largemouth bass varied between 132 and 171 kg ha –1 among the four ponds. This study demonstrated the potential of initial year classes of largemouth bass to maintain high growth rates during their first growing season, which likely will produce trophy-sized fish in a relatively short time.

F1 Largemouth Bass

  • Goldberg, Tony et. al. Increased Infectious Disease Susceptibility Resulting from Outbreeding Depression. Conservation Biology 19(2):455-462.

    Abstract: The mechanisms by which outbreeding depression leads to reduced fitness are poorly understood. We considered the hypothesis that outbreeding can depress fitness by increasing the susceptibility of hybrid individuals and populations to infectious disease. Competitive breeding trials in experimental ponds indicated that outbred largemouth bass ( Micropterus salmoides) crossed from two geographically and genetically distinct populations suffered a reduction in fitness of approximately 14% relative to parental stocks. We measured the comparative susceptibility of these same outbred stocks to a novel viral pathogen, largemouth bass virus. Following experimental inoculation, F2 generation hybrids suffered mortality at a rate 3.6 times higher than either F1 generation hybrids or wild-type parental fish. Analysis of viral loads indicated that viral replication was more rapid in F2 fish than in F1 hybrids or wild-type parental fish. We attribute these results to the disruption of coadapted gene complexes in the immune systems of outbred fish in the F2 generation. Increased susceptibility to infectious disease may be an important but underappreciated mechanism by which outbreeding reduces the fitness of individuals and populations and by which novel infectious diseases emerge in populations of hybrid organisms.

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  • Kassler, T. W., J. B. Koppelman, T. J. Near, et al. 2002. Molecular and morphological analyses of the black basses: implications for taxonomy and conservation. Pages 291-322 in D. P. Philipp and M. S. Ridgeway, editors. Black bass: ecology, conservation, and management. American Fisheries Society, Symposium 31, Bethesda, Maryland.

    Abstract: Taxonomists currently recognize seven species and three subspecies in the genus Micropterus, Based on variation in meristic characters, allozymes, and mtDNA, two subspecies are clearly distinct from one another and warrant elevation to species status. Micropterus salmoides floridanus should now be recognized as the Florida bass M. floridanus, and M. salmoides salmoides as the largemouth bass M. salmoides. Although the Alabama spotted bass M. punctulatus henshalli is morphologically and genetically quite distinct from the northern spotted bass, a thorough taxonomic assessment is still required prior to any revision. The status of a third subspecies, Neosho smallmouth bass M. dolomieu velox, was not investigated. Phylogenetic analyses of mitochondrial DNA sequence variation indicate that the genus is represented by four lineages: (1) smallmouth bass M. dolomieu and spotted bass M. punctulatus; (2) largemouth bass M. salmoides, Florida bass M. floridanus, Suwannee bass M. notius, and Guadalupe bass M. treculi; (3) shoal bass M. cataractae; and (4) redeye bass M. coosae and Alabama spotted bass. It is likely that through either natural or human-induced changes, hybridization has occurred between the Alabama spotted bass and M. coosae and between M. punctulatus and M. treculi, which may have obscured the true phylogenetic affinities of these taxa. In response to this new information, management agencies need to alter their policy toward stocking non-native species and promoting stock transfers. Specifically, they should terminate Florida bass stocking programs outside of Florida.

Florida Bass

  • Florida bass outperformed northern largemouth in this multi-year study.

    https://seafwa.org/sites/default/files/journal-articles/WRIGHT-31-38.pdf

Bluegill

  • Gross, Mart R. & Charnov, Eric L. 1980. Alternative male life histories in bluegill sunfish. Proceedings of the National Academy of Sciences, 77(11): 6937-6940

    Abstract: Male bluegill sunfish are shown to have two alternative mating strategies: cuckoldry or parental care. Cuckolder males first mature at age 2. They follow a developmental sequence of sneaking and then mimicking female behavior to deceptively gain access to spawnings. Males who become parentals (construct nests, attract females, provide brood care) delay maturation until age 7. The parental investment of these males is parasitized by the cuckolders. This system is an example of a truly parasitically dependent mating strategy in vertebrates. A natural selection model is developed to predict the equilibrium frequencies of the two male types. A preliminary test of the model provides qualitative agreement.

  • Jennings, M. J., Claussen, J. E. and Philipp, D. P. 1997. Effect of Population Size Structure on Reproductive Investment of Male Bluegill. North American Journal of Fisheries Management, 17: 516-524.

    Abstract: Although a goal of fisheries management is to understand factors affecting the growth rate and size structure of exploited populations, the relation between growth rates and variation in reproductive behaviors in Lepomis species has received little attention. Allocation of energy to reproductive functions (e.g., gonadal maturation, gamete production, nesting and spawning activities, and brood defense) negatively affects growth rate and, ultimately, maximum body size. To assess how social factors influence energy allocation, we manipulated population size structure of male bluegills L. macrochirus in experimental ponds and evaluated individual reproductive behavior and testes development. We predicted that smaller parental males would invest less in reproduction in the presence of larger parental males than they would in their absence. Observations were consistent with this prediction; smaller parental males had smaller testes and nested less frequently in the presence of larger males than in their absence. Furthermore, when males of both size-groups occupied nests, larger males were more successful. Size-selective angling that removes larger males may, therefore, negatively affect the size structure of Lepomis populations by creating conditions under which smaller, and often younger fish, mature sexually and reproduce. Under those conditions, growth rates would slow at younger ages, and the maximum size attained by these fish would be reduced.

  • Ehlinger, T. J., Gross, M. R., and Philipp, D. P. 1997. Morphological and Growth Rate Differences between Bluegill Males of Alternative Reproductive Life Histories. North American Journal of Fisheries Management, 17: 533-542.

    Abstract: We characterized the morphology of mature cuckolder and mature parental male bluegills Lepomis macrochirus from Lake Opinicon, Ontario. By rearing bluegill larvae to maturity in experimental ponds in Illinois we also examined whether morphological differences between males of the two reproductive life histories were conserved across widely varying environmental conditions. Cuckolder and parental males collected in Lake Opinicon differed in their size-adjusted body shape. They also differed in their pattern of mass allocation to testis versus somatic tissue. Cuckolder males allocated significantly more of their total body mass to testes compared to parental males. Body shape and testis:somatic ratio differences between male types reared in experimental ponds in Illinois were nearly identical to those observed in bluegills from Lake Opinicon. This divergence between male types remained consistent even when bluegills were reared over a 10-fold variation in growth rate. Average growth rate within ponds was strongly associated with the probability that a male would mature as a parental male within the first year. However, the proportion of males maturing as cuckolders was relatively constant among ponds and was not influenced by growth rate differences. These findings have important implications for management of bluegills and other Lepomis species where growth differences or reproductive divergence occur within single populations.

  • Rypel, Andrew L. 2015. Effects of a Reduced Daily Bag Limit on Bluegill Size Structure in Wisconsin Lakes. North American Journal of Fisheries Management, 35:2, 388-397

    Abstract: This study evaluated the effect of reduced aggregate panfish bag limits (from 25 to 10) on the size structure of Bluegill Lepomis macrochirus populations in seven natural lakes in Wisconsin. For assessing the overall significance of treatments, each treatment lake was paired with a control lake in which the regulation was not implemented. Across all lakes, mean total length (TL) of sampled Bluegills was significantly greater in treatment lakes than in control lakes after the regulation was implemented: on average, mean TL increased by 20.3 mm. However, efficacy of reduced bag limits varied substantially across lakes as mean TL improvements ranged from 5.1 to 63.5 mm in individual lakes. This variation could be strongly explained (R2 = 0.81) by lake Secchi depth (lakes with reduced water clarity showed larger improvements in mean TL, R2 = 0.62) and regulation duration (size structure improved continuously with time after the reduced daily bag limit was implemented, R2 = 0.75). Reduced bag limits are a useful tool for providing improvements to Bluegill size structure in Wisconsin lakes, but would be most effective in more productive waterbodies and will require substantial time investments after implementation.

  • Hayward, R.S. and Wang, H.P. 2000. Inherent Growth Capacity and Social Costs of Bluegill and Hybrids of Bluegill and Green Sunfish: Which Fish Really Grows Faster? North American Journal of Aquaculture, 64: 34-46

    Abstract: There is interest in knowing whether the bluegill Lepomis macrochirus or a hybrid of bluegill and green sunfish L. cyanellus (F1: male bluegill   female green sunfish; hereafter called B   G hybrids) can be grown faster to food market size (225–340 g). The predominant view is that the hybrid grows faster. In this study, the inherent growth capacities (IGCs) of age-1 bluegills and B   G hybrids were determined over four successive 25-d periods (May–August 2000) by holding them individually at 22 C and feeding them to apparent satiation three times daily. The hybrid’s IGC was greater during period 1 but fell to only 33% of the bluegill’s over the three subsequent periods; the consumption and gross growth efficiency (GGE) of the hybrid showed similar declining patterns. The growth-in-weight trajectory of bluegills crossed above that of the hybrids at about 30 g. Gonadosomatic index values suggested that hybrid growth rates declined below those of the bluegill because the former invested more energy in gonads as age-1 fish. A follow-up study, conducted under similar conditions from August 2000 to March 2001, found that individually held age-1 bluegills starting at 30 g reached more than 100 g in 200 d, gaining nearly twice the weight achieved by hybrids of similar starting weight that were reared in parallel. The costs of social interaction in terms of reduced consumption, growth, and GGE were also quantified for bluegills and hybrids by comparing individually held fish with group-held fish over periods 1–3. Social costs reduced the growth rates of grouped bluegills more than those of grouped hybrids over the 75-d period. Our findings indicate that while the IGC was higher for the hybrids as early age-1 fish, the long-term IGC (e.g., to food market weights) is higher for bluegills; however, this result may be obscured, in part, by the bluegill’s higher social costs. Reduction of bluegill social costs in certain culture settings should result in growth rates that approach their higher IGC. Also, social costs varied in response to short-term shifts in the IGCs of both fishes, indicating a previously unknown influence on social interactions in fishes.

  • Treml, Melissa & Claussen, Julie & Philipp, David & Pereira, Donald. 1997. A Comparison of Bluegill Reproductive Strategies and Growth among Lakes with Different Fishing Intensities. North American Journal of Fisheries Management, 17: 496-507.

    Abstract: Life history theory suggests that maturation schedules of male bluegill Lepomis macrochirus and the occurrence of alternative male reproductive strategies (i.e., parental or cuckolder) may contribute to the development and duration of undesirable bluegill population size structure (few fish larger than 150 mm). To investigate this relationship, we assessed parental male maturation schedules and relative abundance of cuckolders in six lakes subject to differing levels of fishing effort. Bluegills were collected by electrofishing shortly after the onset of the spawning season. Lakes with lower fishing effort had parental males that were older and larger at maturity than parental males in lakes with high fishing effort. Also, growth of parental males in lakes with low fishing effort was faster at older ages, and growth of immature males was faster than growth of cuckolders. Unlike other lakes, two of the three low-fishing-effort lakes had very few cuckolders. Our results indicate that intense fishing effort is associated with younger ages and smaller sizes at maturity for parental male bluegills. Also, increased proportions of cuckolders may be associated with increased fishing effort.

Supplemental feeding

  • Woodard, Stephen R. et. al. Growth and Survival of Largemouth Bass following Supplemental Feeding of Bluegills in Small Impoundments. North American Journal of Fisheries Management 33(1), February 2013.

    Abstract: We investigated whether providing supplemental pellet feed to Bluegills Lepomis macrochirus in small impoundments increased their growth and reproductive rates after stocking and whether the supplemental feeding of Bluegills had positive indirect effects on Largemouth Bass Micropterus salmoides during the initial stocking year. In 2010, we stocked adult Bluegills and Largemouth Bass into nine 0.1-ha ponds; three replicate ponds were each provided with no pelleted food (control), a low ration (1.52 kg ha−1 d−1), or a high ration (2.68 kg ha−1 d−1). Supplemental feeding yielded increases in the growth of newly stocked Bluegills, the gonadosomatic index of female Bluegills, and the density of larval Bluegills within 4 months of stocking. In contrast, the sizes of adult and age-0 Largemouth Bass and the density and biomass of age-0 Bluegills during fall were not affected by feeding within the time frame of our study. The results demonstrate that supplemental pellet feeding is useful when the management goal is to increase Bluegill size and reproductive output and that these effects develop soon after stocking. We conclude that supplemental feeding is a beneficial enhancement technique for application to Bluegills in recently stocked impoundments.

  • Roy, Luke A. et. al. Weight loss, survival, and fatty acid composition in over-wintered juvenile Coppernose Bluegill ( Lepomis macrochirus purpurescens) cultured in outdoor tanks using different feeding regimens. North American Journal of Aquaculture, August 2021.

    Abstract: Commercial producers raising centrarchids in Arkansas routinely report winter mortality. Juvenile centrarchids are susceptible to harsh winter conditions. Coppernose Bluegill (Lepomis macrochirus purpurescens) is a popular sportfish for recreational fishing and there are no recommended best management practices for winter feeding of this species. An outdoor trial was conducted to investigate the effect of different feeding regimens on performance of Coppernose Bluegill in the winter of 2014/2015. Four feeding regimens were implemented that included feeding twice per week (2x/week), once per week (1x/week), twice per month (2x/month), or once per month (1x/month). Twenty‐five Coppernose Bluegill (initial weight 2.59   0.19 g) were stocked per tank (16 tanks, four replicates). Temperatures ranged from 0–16 C during the trial. After 95 d, there were no differences (P > 0.05) in final weight, or weight loss. Fish fed 2x/week or 1x/week had higher survival (P < 0.05) than those fed 2x/month or 1x/month. Fatty acid profiles of initial fish were distinctly different from those of post winter‐fed bluegill, although winter feeding frequency did not appear to influence fatty acid profiles in coppernose bluegill. Levels of saturates were higher in initial fish than in post‐winter fish. Monosaturates 16:1 and 18:1n‐9 were higher in initial fish than in post‐winter fish. Initial fish contained lower levels of 18:2n–6, 20:4, and 22:6n–3 than post‐winter fish. Total polyunsaturated fatty acids (PUFA), n‐3 and n‐6 levels were also lower in initial fish than post‐winter fish, while the ratio n‐6/n‐3 fatty acids did not differ significantly among initial and post‐winter fed fish. Data indicate that 1) overwintering and infrequently fed Coppernose Bluegill preferentially conserve PUFA, and 2) feeding once or twice per week may be a beneficial strategy for sportfish producers to increase survival of Coppernose Bluegill during the winter in temperate regions of the U.S.

  • Shoup, Daniel E. and Wahl, D.H. Body Size, Food, and Temperature Affect Overwinter Survival of Age-0 Bluegills. Transactions of the American Fisheries Society 140(5):1298-1304, September 2011.

    Abstract: For many species of fish, size-specific overwinter mortality is an important factor structuring year-class strength. Protracted spawning by bluegill Lepomis macrochirus leads to extreme variation in individual size going into winter that could result in strong, size-specific overwinter mortality, particularly in locations with limited food resources or long, cold winters. We performed laboratory trials to test the effects of winter temperature (4 C or 9 C) and food availability (food present or no food) on the survival of two size-classes (20–30 or 50–60 mm total length) of young-of-year bluegills. Mortality was strongly size selective and appeared to be related to relative condition, suggesting that energy limitation was the primary mechanism of mortality. Fish of both sizes were less active at colder temperatures, leading to increased survival (presumably via reduced energy expenditure). Bluegills fed heavily in food treatments (wet weight/d consumed was typically 2–4% for both large and small fish in the warm treatment, 1–2.5% for small fish in the cold treatment, and 0.4–0.8% for large fish in the cold treatment) and experienced increased survival. However, small fish in all treatments had more than 55% mortality after 150 d, indicating that some of the mortality was not due to starvation. It appears that late-spawned, small fish are unlikely to survive lengthy periods of winter conditions and will therefore be selected against at northern latitudes. Mechanisms other than overwinter mortality that lead to increased lifetime reproductive success may explain the persistence of late-summer or fall spawning at these latitudes.

  • Stump, Andrew J. (2022). Bluegill Response to Supplemental Feeding and Patch Richness in Recreational Fishing Ponds.

    Abstract: From recreation to aquaculture to commercial fisheries, the study of aquatic systems are essential for maintaining and understanding how nutrient flow and population dynamics are affected using specific management techniques. This thesis paper is centered on a pure research topic dedicated towards exploring whether supplemental feeding in managed ponds creates two distinct populations of bluegill (Lepomis macrochirus) within a pond system. The ponds in this study were subjected to three separate, two-week trials of supplemental feeding. Relative weights of individuals caught at designated feeding and non-feeding patches were used to determine if fish condition was significantly different at fed patches when compared to non-fed patches. Stratification of individuals within the system was seen on a significant level depending on the sites where fish were captured thus leading to the likelihood that feeding directly alters the location of fish with a higher average body condition. This baseline study may help further the understanding of how supplemental feeding distributes pond populations and lead to the implementation of more balanced, pond specific management practices when considering supplemental feed as a management strategy.

Fertilization

  • Smith, E. & Swingle, H.. (1941). Winter and Summer Growth of Bluegills in Fertilized Ponds. Transactions of the American Fisheries Society. 70. 335-338.

    Abstract: The use of fertilizers to increase the production of fish in ponds has become widespread in recent years. Since fish are cold-blooded animals, their metabolic activities are slowed by cold weather and accelerated by hot weather. Experiments were conducted to study the winter and summer growth of bluegill bream. In December, small fertilized ponds were stocked with bluegill fingerlings at the rate of 1,750 per acre, individuals averaging 3.8 grams in weight. Three months later their average weight had increased to 11.4 grams, a gain of 200 per cent. The water temperature during this period varied from 3  C. in January to 15  C. in March. Another fertilized pond was stocked in March at the rate of 1,500 fingerlings per acre, individuals averaging 4.5 grams in weight. Samples of bream taken from this pond in June averaged 80 grams, a gain of 1,700 per cent. The water temperature during the latter period ranged from 19  C. to 24  C.

  • Boyd, Claude. (2018). Aquaculture pond fertilization. CAB Reviews: Perspectives in Agriculture, Veterinary Science, Nutrition and Natural Resources. 13.

    Abstract: Organic fertilizers (livestock manures and other agricultural wastes or by-products) and chemical fertilizers can be applied to aquaculture ponds to increase fish or shrimp production. Pond fertilization increases concentrations of nitrogen, phosphorus and other plant nutrients to stimulate phytoplankton photosynthesis that is the base of the food web culminating in shrimp and fish production. Fertilization usually results in two to fivefold increase in aquaculture production. Organic fertilizers tend to increase production above that possible with chemical fertilizers, but a combination of organic and chemical fertilization usually results in greater production than does either type of fertilization alone. Manufactured feeds allow much greater production than possible with fertilizers, and feeding has become more common than pond fertilization. However, fertilization remains an important practice for smallholder farmers in developing countries. It also is sometimes applied early in the grow-out period in feed-based aquaculture, and it is a common technique for increasing production of sportfish ponds.

Stocking Fathead Minnows

Grass Shrimp

Grass Carp

  • Kilgen, Ronald H. & Smitherman, R. Oneal. 1971. Food Habits of the White Amur Stocked in Ponds Alone and in Combination with other Species. The Progressive Fish-Culturist, 33:3, 123-127.

  • Forester, Timothy S; Lawrence, John M. Effects of grass carp and carp on populations of bluegill and largemouth bass in ponds. Transactions of the American Fisheries Society, Vol. 107 no. 1 (1978), p. 172 - 175.