Skip to main content

Wetland Fish Monitoring and Assessment

  • Chapter
  • First Online:
Wetland Techniques

Abstract

Fish sampling is an important component of wetland research, management, conservation, monitoring, and assessment programs, and studies of fish abundance, productivity, and community structure can provide important information about wetland condition and health. In this chapter, we discuss considerations specific to wetland sampling, including issues such as the phenology of wetland use by transient fishes and sampling constraints in hydrologically-dynamic habitats. We review both active techniques, which involve moving the gear to the fish, and passive techniques, which involve the fish moving to the gear, and differentiate gears based on their ability to provide qualitative or quantitative data. Because wetlands vary considerably in their hydrology, physicochemistry, habitat structure and biotic community composition, we review and recommend a wide variety of collection techniques, including seines, minnow traps, gill and entrapment nets, electrofishing, throw and drop traps, weirs, and trawls. Problems and solutions related to gear calibration and gear bias also are addressed, and we provide examples and exercises that demonstrate common approaches to sampling wetland fishes.

This is a preview of subscription content, log in via an institution to check access.

Access this chapter

Chapter
USD 29.95
Price excludes VAT (USA)
  • Available as PDF
  • Read on any device
  • Instant download
  • Own it forever
eBook
USD 84.99
Price excludes VAT (USA)
  • Available as EPUB and PDF
  • Read on any device
  • Instant download
  • Own it forever
Softcover Book
USD 109.99
Price excludes VAT (USA)
  • Compact, lightweight edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info

Tax calculation will be finalised at checkout

Purchases are for personal use only

Institutional subscriptions

References

  • Abell R, Thieme ML, Revenga C, Bryer M, Kottelat M, Bogutskaya N, Coad B, Mandrak N, Contreras Balderas S, Bussing W, Stiassny ML, Skelton P, Allen GR, Unmack P, Naseka A, Ng R, Sindork N, Roberton J, Armijo E, Higgins JV, Heibel TJ, Wikramanayake E, Olson D, Lopez HL, Reis RE, Lundberg JG, Sabaj Perez MH, Perty P (2008) Freshwater ecoregions of the world: a new map of biogeographic units for freshwater biodiversity conservation. Bioscience 58:403–414

    Article  Google Scholar 

  • Able KW, Nemerson DM, Bush R, Light P (2001) Spatial variation in Delaware Bay (U.S.A.) marsh creek fish assemblages. Estuaries 24:441–452

    Article  Google Scholar 

  • Acreman MC, Fisher J, Stratford CJ, Mould DJ, Mountford JO (2007) Hydrological science and wetland restoration: some case studies from Europe. Hydrol Earth Syst Sci 11:158–169

    Article  CAS  Google Scholar 

  • Adams NS, Rondorf DW, Evans SD, Kelly JE (1998) Effects of surgically and gastrically implanted radio transmitters on growth and feeding behavior of juvenile Chinook salmon. Trans Am Fish Soc 127:128–136

    Article  Google Scholar 

  • Adams AJ, Wolfe RK, Pine WE III, Thornton BL (2006) Efficacy of PIT tags and an autonomous antenna system to study the juvenile life stage of an estuarine-dependent fish. Estuar Coast 29:311–317

    Article  Google Scholar 

  • Akin S, Winemiller KO, Gelwick FP (2003) Seasonal and spatial variation in fish and macrocrustacean assemblage structure in Mad Island Marsh estuary, Texas. Estuar Coast Shelf Sci 57:269–282

    Article  Google Scholar 

  • Allen MJ, Herbinson KT (1991) Beam-trawl survey of bay and nearshore fishes of the soft-bottom habitat of southern California in 1989. CalCOFI 32:112–127

    Google Scholar 

  • Allen DM, Service SK, Ogburn-Matthews MV (1992) Factors influencing the collection efficiency of estuarine fish. Trans Am Fish Soc 121:234–244

    Article  Google Scholar 

  • American Society of Ichthyologists and Herpetologists, American Fisheries Society, American Institute of Fisheries Research Biologists (1988) Guidelines for use of fish in field research. Fisheries 13:16–23

    Google Scholar 

  • Angradi TR (1992) Effects of predation risk on foraging behavior of juvenile rainbow trout (Oncorhynchus mykiss). Can J Zool 70:355–360

    Article  Google Scholar 

  • Baber MJ, Childers DL, Babbitt KJ, Anderson DH (2002) Controls on fish distribution and abundance in temporary wetlands. Can J Fish Aquat Sci 59:1441–1450

    Article  Google Scholar 

  • Bacon PJ, Gurney WSC, McKenzie E, Whyte B, Campbell R, Laughton R, Smith G, MacLean J (2011) Objective determination of the sea age of Atlantic salmon from sizes and dates of capture of individual fish. ICES J Mar Sci 68:130–143

    Article  Google Scholar 

  • Bagenal TB (1974) A buoyant net designed to capture freshwater fish larvae quantitatively. Freshw Biol 4:107–109

    Article  Google Scholar 

  • Bakus GJ, Nishiyama G, Hajdu E, Mehta H, Mohammed M, dos San PU, Sohn SA, Pham TK, bin Yasin Z, Shau-Hwai T, Karam A, Hanan E (2007) A comparison of some population density techniques for biodiversity, conservation, and environmental impact studies. Biodivers Conserv 16:2445–2455

    Article  Google Scholar 

  • Bardygula-Nonn LG, Nonn R, Savitz J (1995) Influence of pulsed direct current electrofishing on mortality and injuries among four centrarchid species. N Am J Fish Manag 15:799–803

    Article  Google Scholar 

  • Basler MC, Schramm HL Jr (2006) Evaluation of electrofishing and fyke netting for collecting black carp in small ponds. Trans Am Fish Soc 135:277–280

    Article  Google Scholar 

  • Batzer DP (1998) Trophic interactions among detritus, benthic midges, and predatory fish in a freshwater marsh. Ecology 79:1688–1698

    Article  Google Scholar 

  • Batzer DP, Putsateri CR, Vetter R (2000) Impacts of fish predation on marsh invertebrates: direct and indirect effects. Wetlands 20:307–312

    Article  Google Scholar 

  • Bayley PB, Larimore RW, Dowling DC (1989) Electric seine as a fish-sampling gear in streams. Trans Am Fish Soc 118:447–453

    Article  Google Scholar 

  • Beck MW, Heck KL Jr, Able KW, Childers DL, Eggleston DB, Gillanders BM, Halpern B, Hays CG, Hoshino K, Minello TJ, Orth RJ, Sheriden PF, Weinstein MP (2001) The identification, conservation, and management of estuarine and marine nurseries for fish and invertebrates. Bioscience 51:633–641

    Article  Google Scholar 

  • Beesley LS, Gilmour JP (2008) A modified drop net for sampling fish communities in complex habitats: a description and comparison with other techniques. N Am J Fish Manag 28:1214–1222

    Article  Google Scholar 

  • Berry CR Jr, Dennerline D, Rulifson R (2012) Safety: skills, attitudes, facts, and equipment. In: Zale AV, Parrish DL, Sutton TM (eds) Fisheries techniques, 3rd edn. American Fisheries Society, Bethesda, pp 79–100

    Google Scholar 

  • Bhagat Y, Ciborowski JJH, Johnson LB, Uzarski DG, Burton TM, Timmermans STA, Cooper MJ (2007) Testing a fish index of biotic integrity for responses to different stressors in Great Lakes coastal wetlands. J Great Lakes Res 33:224–235

    Article  Google Scholar 

  • Bilkovic DM, Roggero MM (2008) Effects of coastal development on nearshore estuarine nekton communities. Mar Ecol Prog Ser 358:27–39

    Article  Google Scholar 

  • Bobsien IC, Brendelberger H (2006) Comparison of an enclosure drop trap and a visual diving census. Limnol Ocean Methods 4:130–141

    Article  Google Scholar 

  • Bohlin T, Heggbert TG, Strange C (1990) Electric fishing for sampling and stock assessment. In: Cowx IG, Lamarque P (eds) Fishing with electricity, applications in freshwater fisheries management. Fishing News Books, Oxford, pp 112–139

    Google Scholar 

  • Bonar SA, Contreras-Balderas S, Iles AC (2009) An introduction to standardized sampling. In: Bonar SA, Hubert WA, Willis DA (eds) Standard methods for sampling North American freshwater fishes. American Fisheries Society, Bethesda, pp 1–12

    Google Scholar 

  • Booth AJ, Potts WM (2006) Estimating gill-net selectivity for Labeo umbratus (Pisces: Cyprinidae), and an evaluation of using fyke-nets as a non-destructive sampling gear in small reservoirs. Fish Res 79:202–209

    Article  Google Scholar 

  • Boswell KM, Wilson MP, Wilson CA (2007) Hydroacoustics as a tool for assessing fish biomass and size distribution associated with discrete shallow water estuarine habitats in Louisiana. Estuar Coast 30:607–617

    Google Scholar 

  • Boswell KM, Wilson MP, Cowan JH Jr (2008a) A semiautomated approach to estimating fish size, abundance, and behavior from dual-frequency identification sonar (DIDSON) data. N Am J Fish Manag 28:799–807

    Article  Google Scholar 

  • Boswell KM, Kaller MD, Cowan JH Jr, Wilson CA (2008b) Evaluation of target strength-fish length equations for estimating estuarine biomass. Hydrobiologia 258:1456–1464

    Google Scholar 

  • Boswell KM, Wilson MP, MacRae PSD, Wilson CA, Cowan JH Jr (2010) Seasonal estimates of fish biomass and length distributions using acoustics and traditional nets to identify estuarine habitat preferences in Barataria Bay, Louisiana. Mar Coast Fish Dyn Manag Ecosyst Sci 2:83–97

    Article  Google Scholar 

  • Bouvier LD, Cottenie K, Doka SE (2009) Aquatic connectivity and fish metacommunities in wetlands of the lower Great Lakes. Can J Fish Aquat Sci 66:933–948

    Article  Google Scholar 

  • Brady VJ, Ciborowski JJH, Johnson LB, Danz NP, Holland JD, Breneman DH, Gathman JP (2007) Optimizing fishing time: one vs. two-night fyke net sets in Great Lakes Coastal Systems. J Great Lakes Res 33:236–244

    Article  Google Scholar 

  • Brazner JC (1997) Regional, habitat, and human development influences on coastal wetland and beach fish assemblages in Green Bay, Lake Michigan. J Great Lakes Res 23:36–51

    Article  Google Scholar 

  • Brazner JC, Beals EW (1997) Patterns in fish assemblage from coastal wetland and beach habitats in Green Bay, Lake Michigan: a multivariate analysis of abiotic and biotic forcing factors. Can J Fish Aquat Sci 54:1743–1761

    Article  Google Scholar 

  • Breine J, Quataert SM, Ollevier F, Volckaert FAM, Van den Bergh E, Maes J (2010) A zone-specific fish-based index as a management tool for the Zeeschelde estuary (Belgium). Mar Pollut Bull 60:1099–1112

    Article  PubMed  CAS  Google Scholar 

  • Brosse S, Laffaille P, Gabas S, Lek S (2001) Is scuba sampling a relevant method to study fish microhabitat in lakes? Examples and comparisons for three European species. Ecol Fresh Fish 10:138–146

    Article  Google Scholar 

  • Brown RS, Cooke SJ, Anderson WG, McKinley RS (1999) Evidence to challenge the “2 % Rule” for biotelemetry. N Am J Fish Manag 19:867–871

    Article  Google Scholar 

  • Brown RS, Eppard MB, Murchie KJ, Nielsen JL, Cooke SJ (2011) An introduction to the practical and ethical perspectives on the need to advance and standardize the intracoelomic surgical implantation of electronic tags in fish. Rev Fish Biol Fish 21:1–9

    Article  Google Scholar 

  • Brown ML, Allen MS, Beard TD Jr (2012) Data management and statistical techniques. In: Zale AV, Parrish DL, Sutton TM (eds) Fisheries techniques, 3rd edn. American Fisheries Society, Bethesda, pp 15–78

    Google Scholar 

  • Buckley RM, Blankenship HL (1990) Internal extrinsic identification systems: overview of implanted wire tags, otolith marks, and parasites. Am Fish Soc Symp 7:30–35

    Google Scholar 

  • Bulkowski L, Meade JW (1983) Changes in phototaxis during early development of walleye. Trans Am Fish Soc 112:445–447

    Article  Google Scholar 

  • Burns AD (2007) Comparison of two electrofishing gears (backpack and parallel wires) and abundances of fishes in the upper Greenbrier River drainage. MS thesis. West Virginia University, Morgantown

    Google Scholar 

  • Bush Thom CS, LaPeyre MK, Nyman JA (2004) Evaluation of nekton use and habitat characteristics of restored Louisiana marsh. Ecol Eng 23:63–75

    Article  Google Scholar 

  • Carlson JK, Mroczka ME, Randall TA, Pellegrino PE (2000) A comparison of the relative abundance and size of juvenile winter flounder, Pseudopleuronectes americanus, in natural intertidal and anthropogenically altered marine habitats. J Northw Atl Fish Sci 26:37–44

    Article  Google Scholar 

  • Castellanos DL, Rozas LP (2001) Nekton use of submerged aquatic vegetation, marsh, and shallow unvegetated boom in the Atchafalaya River delta, a Louisiana tidal freshwater ecosystem. Estuaries 24:184–197

    Article  Google Scholar 

  • Catalano MJ, Chipps SR, Bouchard MA, Wahl DA (2001) Evaluation of injectable fluorescent tags for marking centrarchid fishes: retention rate and effects on vulnerability to predation. N J Am Fish Manag 21:911–917

    Article  Google Scholar 

  • Chapman LJ, Mckenzie DJ (2009) Behavioral responses and ecological consequences. In: Richards JG, Farrell AP, Brauner CJ (eds) Fish physiology, vol 27, Hypoxia. Elsevier, San Diego, pp 25–77

    Google Scholar 

  • Chick JH, Jordan F, Smith JP, McIvor CC (1992) A comparison of four enclosure traps and methods used to sample fishes in aquatic macrophytes. J Freshw Ecol 7:353–361

    Article  Google Scholar 

  • Chick JH, Coyne S, Trexler JC (1999) Effectiveness of airboat electrofishing for sampling fishes in shallow, vegetated habitats. N J Am Fish Manag 19:957–967

    Article  Google Scholar 

  • Chick JH, Ruetz CR II, Trexler JC (2004) Spatial scale and abundance patterns of large fish communities in freshwater marshes of the Florida Everglades. Wetlands 24:652–664

    Article  Google Scholar 

  • Chu DLH, Li WVT, Yu RMK (2010) Leptin: clue to poor appetite in oxygen-starved fish. Mol Cell Endocrinol 319:143–146

    Article  PubMed  CAS  Google Scholar 

  • Clark-Kolaks SJ, Jackson JR, Lochman SE (2009) Adult and juvenile paddlefish in floodplain lakes along the lower White River, Arkansas. Wetlands 29:488–496

    Article  Google Scholar 

  • Collazo JA, Gilliam JF, Miranda-Castro L (2010) Functional response models to estimate feeding rates of wading birds. Waterbirds 33:33–40

    Article  Google Scholar 

  • Connolly RM (1999) Saltmarsh as habitat for fish and nektonic crustaceans: challenges in sampling design and methods. Aust J Ecol 24:422–430

    Article  Google Scholar 

  • Connolly RM, Dalton A, Bass DA (1997) Fish use of an inundated saltmarsh flat in a temperate Australian estuary. Aust J Ecol 22:22–226

    Google Scholar 

  • Cooke SJ, Hinch SG, Lucas MC, Lutcavage M (2012) Biotelemetry and biologging. In: Zale AV, Parrish DL, Sutton TM (eds) Fisheries techniques, 3rd edn. American Fisheries Society, Bethesda, pp 819–882

    Google Scholar 

  • Copp GH, Penaz M (1988) Ecology of fish spawning and nursery zones in the flood plain, using a new sampling approach. Hydrobiologia 169:209–224

    Article  Google Scholar 

  • Corcoran MF (1979) Electrofishing for catfish: use of low-frequency pulsed direct current. Prog Fish Cult 41:200–201

    Article  Google Scholar 

  • Crawford RE, Jorgenson J (1990) Density distribution of fish in the presence of whales at the Admiralty Inlet landfast ice edge. Arctic 43:215–222

    Google Scholar 

  • Crawford RE, Jorgenson J (1996) Quantitative studies of Arctic cod, Boreogadus saida school: important energy stores in the Arctic food webs. Arctic 49:181–193

    Google Scholar 

  • Cross TK, McInery MC, Schupp DH (1995) Season variation in trap-net catches of bluegill in Minnesota lakes. N Am Fish Manag 15:382–389

    Article  Google Scholar 

  • da Silva HP, Petry AC, da Silva CJ (2010) Fish communities of the Pantanal wetland in Brazil: evaluating the effects of the upper Paraguay River flood pulse on baía Caiçara fish fauna. Aquat Ecol 44:275–288

    Article  CAS  Google Scholar 

  • Dauwalter DC, Fisher WL (2007) Electrofishing capture probability of smallmouth bass in streams. N Am J Fish Manag 27:162–171

    Article  Google Scholar 

  • DeAngelis DL, Trexler JC, Loftus WF (2005) Life history trade-offs and community dynamics of small fishes in a seasonally pulsed wetland. Can J Fish Aquat Sci 62:781–790

    Article  Google Scholar 

  • Dennis B, Ponciano JM, Lele SR, Taper ML, Staples DF (2006) Estimating density dependence, process noise, and sampling error. Ecol Appl 323–341

    Google Scholar 

  • Dewey MR, Holland-Bartels LE, Zigler SJ (1989) Comparison of fish catches with buoyant pop nets and seines in vegetated and unvegetated habitats. N Am J Fish Manag 7:252–259

    Google Scholar 

  • DiBenedetto K (2009) Comparative ecology of alligator gar Atractosteus spatula in brackish and freshwater habitats in Louisiana. MS thesis. Louisiana State University, Baton Rouge

    Google Scholar 

  • Dinger EC, Marks JC (2007) Effects of high levels of antimycin A on aquatic invertebrates in a warmwater Arizona stream. N Am J Fish Manag 27:1243–1256

    Article  Google Scholar 

  • Dolan CR, Miranda LE (2004) Injury and mortality of warmwater fishes immobilized by electrofishing. N Am J Fish Manag 24:118–127

    Article  Google Scholar 

  • Dorn NJ, Urgelles R, Trexler JC (2005) Evaluating active and passive sampling methods to quantify crayfish density in a freshwater marsh. J N Am Bentholl Soc 24:346–356

    Article  Google Scholar 

  • Dotson T (1982) Mortalities in trout caused by gear type and angler-induced stress. N Am J Fish Manag 2:60–65

    Article  Google Scholar 

  • Dresser BK, Kneib RT (2007) Site fidelity and movement patterns of wild subadult red drum, Sciaenops ocellatus (Linnaeus), within a salt marsh-dominated estuarine landscape. Fish Manag Ecol 14:183–190

    Article  Google Scholar 

  • Dumont SC, Dennis JA (1997) Comparison of day and night electrofishing in Texas reservoirs. N Am J Fish Manag 17:939–946

    Article  Google Scholar 

  • Dunson WA, Martin RA (1973) Survival of brook trout in a bog-derived acidity gradient. Ecology 54:1370–1376

    Article  Google Scholar 

  • Dussaillant A, Galdames P, Sun C-L (2009) Water level fluctuations in a coastal lagoon: El Yali Ramsar wetland, Chile. Desalination, pp 202–214

    Google Scholar 

  • Elliot M, Whitfield AK, Potter IC, Blaber SJM, Cyrus DP, Nordlie FG, Harrison TD (2007) The guild approach to categorizing estuarine fish assemblages: a global review. Fish Fish 8:241–268

    Article  Google Scholar 

  • Evans S, Tallmark B (1979) A modified drop-net method for sampling mobile epifauna on marine shallow sandy bottoms. Holoartic Ecol 2:58–64

    Google Scholar 

  • Fago D (1998) Comparison of littoral fish assemblages with a mini-fyke net or with a combination of electrofishing and beach seine in Wisconsin lakes. N Am J Fish Manag 18:731–738

    Article  Google Scholar 

  • Fernandes CC (1997) Lateral migration of fishes in Amazon floodplains. Ecol Freshw Fish 6:36–44

    Article  Google Scholar 

  • Fernandes B, Achuthankutty CT (2010) Seasonal variation in fishery diversity of some wetlands of the Salcete Taluka, Goa, India. Indian J Mar Sci 39:238–247

    Google Scholar 

  • Finlayson B, Somer WL, Vinson MR (2010) Rotenone toxicity to rainbow trout and several mountain stream insects. N Am J Fish Manag 30:102–111

    Article  Google Scholar 

  • Fisheries Society of the British Isles (2006) Ethical justification for the use and treatment of fishes in research. J Fish Biol 68:1–2

    Google Scholar 

  • Fisheries Society of the British Isles (2011) Ethical justification for the use and treatment of fishes in research. J Fish Biol 78:393–394

    Article  Google Scholar 

  • Fishman AP, Pack AI, Delaney RG, Galante RJ (1986) Estivation in Protopterus. J Morphol 190:237–248

    Article  Google Scholar 

  • Foote KG (1987) Fish target strengths for use in echo integrator surveys. J Acoust Soc Am 82:981–987

    Article  Google Scholar 

  • Franco A, Franzoi P, Malavasi S, Riccato F, Torricelli P, Mainardi D (2006) Use of shallow water habitats by fish assemblages in a Mediterranean coastal lagoon. Estuar Coast Shelf Sci 66:67–83

    Article  Google Scholar 

  • Franco A, Torricelli P, Franzoi P (2009) A habitat-specific fish-based approach to assess the ecological status of Mediterranean coastal lagoons. Mar Pollut Bull 58:1407–1717

    Article  CAS  Google Scholar 

  • Galatowitsch SM, Whited DC, Tester JR (1999) Development of community metrics to evaluate recovery of Minnesota wetlands. J Aquat Ecosyst Stress Recov 6:217–234

    Google Scholar 

  • Gebhards SV (1996) Appendix 6.1 repairing gill nets. In: Murphy BR, Willis DW (eds) Fisheries techniques, 2nd edn. American Fisheries Society, Bethesda, pp 182–192

    Google Scholar 

  • Gelwick FP, Akin S, Arrington DA, Winemiller KO (2001) Fish assemblage structure in relation to environmental variation in a Texas Gulf coastal wetland. Estuaries 24:285–296

    Article  Google Scholar 

  • Gerlotto F, Georgakarakos S, Eriksen PK (2000) The application of multibeam sonar technology for quantitative estimates of fish density in shallow water acoustic surveys. Aquat Living Resour 13:385–393

    Article  Google Scholar 

  • Gilchrest WR, Schmidt RE (1997) Comparison of fish communities in open and occluded freshwater tidal wetlands in the Hudson River estuary. Section IX. In: Waldman JR, Nieder WC (eds) Final reports of the Tibor T. Polgar Fellowship Program. Hudson River Foundation, New York, pp 1–32

    Google Scholar 

  • Giles N (1984) Development of the overhead fright response in wild and predator-naive three-spined sticklebacks, Gasterosteus aculeatus L. Anim Behav 32:276–279

    Article  Google Scholar 

  • Goldenstein RM, Meador MR (2004) Comparison of fish species traits from small streams to large rivers. Trans Am Fish Soc 133:971–983

    Article  Google Scholar 

  • Goldenstein RM, Meador MR (2005) Multilevel assessment of fish species traits to evaluate habitat degradation in streams of the upper Midwest. N Am J Fish Manag 25:180–194

    Article  Google Scholar 

  • Grabowski TB, Ferguson TD, Peterson JT, Jennings CA (2009) Capture probability and behavioral response of robust redhorse, a cryptic riverine fish, to electrofishing. N Am J Fish Manag 29:721–729

    Article  Google Scholar 

  • Gregory RS, Powles PM (1985) Chronology, distribution, and sizes of larval fish sampled by light traps in macrophytic Chemung Lake. Can J Zool 63:2569–2577

    Article  Google Scholar 

  • Gresswell RE (1991) The use of antimycin for the removal of brook trout from a tributary of Yellowstone Lake. N Am J Fish Manag 11:83–90

    Article  Google Scholar 

  • Grixti D, Conron SD, Jones PL (2007) The effect of hook/bait size and angling technique on the hooking location and the catch of recreationally caught black bream Acanthopagrus butcheri. Fish Res 84:338–344

    Article  Google Scholar 

  • Guest MA, Connolly RM, Loneragan NR (2003) Seine nets and beam trawls compared by day and night for sampling fish and crustaceans in shallow seagrass habitat. Fish Res 64:185–196

    Article  Google Scholar 

  • Guillory V (1993) Ghost fishing by blue crab traps. N Am J Fish Manag 13:459–466

    Article  Google Scholar 

  • Habera JW, Strange RJ, Carter BD (1996) Short-term mortality and injury of Rainbow Trout caused by three-pass AC electrofishing in a southern Appalachian stream. N Am J Fish Manag 16:192–200

    Article  Google Scholar 

  • Hagy JD, Boynton WR, Keefe CW, Wood KV (2004) Hypoxia in Chesapeake Bay, 1950–2001: long-term change in relation to nutrient loading and river flow. Estuaries 27:634–658

    Article  CAS  Google Scholar 

  • Hale RS, Gray JH (1998) Retention and detection of coded wire tags and elastomer tags in trout. N Am J Fish Manag 18:197–201

    Article  Google Scholar 

  • Hamilton BT, Moore SE, Williams TB, Darby N, Vinson MR (2009) Comparative effects of rotenone and antimycin on macroinvertebrate diversity in two streams in Great Basin National Park, Nevada. N Am J Fish Manag 29:1620–1635

    Article  Google Scholar 

  • Hamley JM (1975) Review of gillnet selectivity. Can J Fish Aquat Sci 32:1943–1969

    Google Scholar 

  • Hamley JM (1980) Sampling with gill nets. In: T Backiel, RL Welcomme (eds) Guidelines for sampling fish in inland waters. FAO European Inland Fisheries Advisory Commission technical paper 33, Rome, Italy, pp 37–53

    Google Scholar 

  • Hamley JM, Howley TP (1985) Factors affecting the variability of trapnet catches. Can J Fish Aquat 42:1079–1087

    Article  Google Scholar 

  • Hanson MA, Riggs MR (1995) Potential effects of fish predation on wetland invertebrates: a comparison of wetlands with and without fathead minnows. Wetlands 15:167–175

    Article  Google Scholar 

  • Harrison TD, Whitfield AK (2006) Application of a multimetric fish index to assess the environmental condition of South African estuaries. Estuar Coast 29:1108–1120

    Google Scholar 

  • Hartman KJ, Nagy BW (2005) A target strength and length relationship for striped bass and white perch. Trans Am Fish Soc 134:375–380

    Article  Google Scholar 

  • Hayer CA, Irwin ER (2008) Influence of gravel mining and other factors on detection probabilities of coastal plain fishes in the Mobile River basin, Alabama. Trans Am Fish Soc 137:1606–1620

    Article  Google Scholar 

  • Hayes JW (1989) Comparison between fine mesh trap net and five other fishing gears for sampling shallow-lake fish communities in New Zealand. N Z J Mar Fresh 23:321–324

    Article  Google Scholar 

  • Hayes DB, Bence JR, Kwak TJ, Thompson BE (2007) Abundance, biomass, and production. In: Guy CS, Brown ML (eds) Analysis and interpretation of freshwater fisheries data. American Fisheries Society, Bethesda, pp 327–374

    Google Scholar 

  • Hayes DB, Ferreri CP, Taylor WW (2012) Active fish capture methods. In: Zale AV, Parrish DL, Sutton TM (eds) Fisheries techniques, 3rd edn. American Fisheries Society, Bethesda, pp 267–304

    Google Scholar 

  • He X, Lodge DM (1990) Using minnow traps to estimate fish population size: the importance of spatial distribution and relative species abundance. Hydrobiologia 190:9–14

    Article  Google Scholar 

  • Hering DK, Bottom DL, Prentice EF, Jones KK, Fleming IA (2010) Tidal movements and residency of subyearling Chinook salmon (Oncorhynchus tshawytscha) in an Oregon salt marsh channel. Can J Fish Aquat Sci 67:524–533

    Article  Google Scholar 

  • Hettler WF Jr (1989) Nekton use of regularly-flooded saltmarsh cordgrass habitat in North Carolina, USA. Mar Ecol Prog Ser 56:111–118

    Article  Google Scholar 

  • Hewitt DP (1979) Tests to confirm quantitative sampling of young fish by the Bagenal buoyant net. Freshw Biol 9:339–341

    Article  Google Scholar 

  • Hewitt JE, Thrush SF (2007) Effective long-term ecological monitoring using spatially and temporally nested sampling. Environ Monit Assess 133:295–307

    Article  PubMed  CAS  Google Scholar 

  • Higer AL, Kolipinski MC (1967) Pull-up trap: a quantitative device for sampling shallow-water animals. Ecology 48:1008–1009

    Article  Google Scholar 

  • Hill TD, Willis DW (1994) Influence of water conductivity on pulsed AC and pulsed DC electrofishing catch rates for largemouth bass. N Am J Fish Manag 14:202–207

    Article  Google Scholar 

  • Hirst CN, Jackson DA (2007) Reconstructing community relationships: the impact of sampling error, ordination approach, and gradient length. Divers Distrib 13:361–371

    Article  Google Scholar 

  • Hitt PF, Angermeier PL (2011) Fish community and bioassessment responses to stream network position. J N Am Bentholl Soc 30:296–309

    Article  Google Scholar 

  • Hopkins TE, Cech JJ Jr (1992) Physiological effects of capturing striped bass in gill nets and fyke traps. Trans Am Fish Soc 121:819–822

    Google Scholar 

  • Hubert WA, Pope KL, Dettmers JM (2012) Passive capture techniques. In: Zale AV, Parrish DL, Sutton TM (eds) Fisheries techniques, 3rd edn. American Fisheries Society, Bethesda, pp 223–266

    Google Scholar 

  • Jackson JR, Noble RL (1995) Selectivity of sampling methods for juvenile largemouth bass in assessments of recruitment processes. N Am J Fish Manag 15:408–418

    Article  Google Scholar 

  • Jacobsen T, Kushlan JA (1987) Sources of sampling bias in enclosure fish trapping: effects on estimates of density and diversity. Fish Res 5:401–412

    Article  Google Scholar 

  • Janáč M, Juradja P (2007) A comparison of point abundance and continuous sampling by electrofishing for age-0 fish in a channelized lowland river. N Am J Fish Manag 27:1115–1119

    Article  Google Scholar 

  • Jeffries DS, Semkiin RG, Gibson JJ, Wong I (2010) Recently surveyed lakes in northern Manitoba and Saskatchewan, Canada: characteristics and critical loads of acidity. J Limnol 69:45–55

    Article  Google Scholar 

  • Jennings CE, Sloss BL, Lasee BA, Burtle GJ, Moyer GR (2012) Care, handling, and examination of sampled organisms. In: Zale AV, Parrish DL, Sutton TM (eds) Fisheries techniques, 3rd edn. American Fisheries Society, Bethesda, pp 163–222

    Google Scholar 

  • Jepsen N, Davis LE, Schreck CB, Siddens B (2001) The physiological response of Chinook salmon smolts to two methods of radio-tagging. Trans Am Fish Soc 130:495–500

    Article  Google Scholar 

  • Jepsen N, Koed A, Thorstad EB, Baras E (2002) Surgical implantation of telemetry transmitters in fish: how much have we learned? Hydrobiologia 438:239–248

    Article  Google Scholar 

  • Jester DB (1977) Effects of color, mesh size, fishing in seasonal concentrations, and baiting on catch rates of fishes in gill nets. Trans Am Fish Soc 106:43–56

    Article  Google Scholar 

  • Jordan F, Coyne S, Trexler JC (1997) Sampling fishes in vegetated habitats: effects of habitat structure on sampling characteristics of the 1-m2 throw trap. Trans Am Fish Soc 126:1012–1020

    Article  Google Scholar 

  • Jordan F, Babbitt FJ, McIvor CC (1998) Season variation in habitat use by marsh fishes. Ecol Freshw Fish 7:159–168

    Article  Google Scholar 

  • Jude DJ, Pappas J (1992) Fish utilization of Great Lakes wetlands. J Great Lakes Res 18:651–672

    Article  Google Scholar 

  • Kahl MP Jr (1963) Technique for sampling population density of small shallow-water fish. Limnol Ocean 8:302–304

    Article  Google Scholar 

  • Kanouse S, LaPeyre MK, Nyman JA (2006) Nekton use of Ruppia maritima and non-vegetated habitat types within brackish marsh ponds. Mar Ecol Prog Ser 327:51–59

    Article  Google Scholar 

  • Kelso WE (1979) Predation on soft-shell clams, Mya arenaria, by the common mummichog Fundulus heteroclitus. Estuaries 2:249–254

    Article  Google Scholar 

  • Kelso WE, Kaller MD, Rutherford DA (2012) Collection, processing, and identification of fish eggs and larvae, and zooplankton. In: Zale AV, Parrish DL, Sutton TM (eds) Fisheries techniques, 3rd edn. American Fisheries Society, Bethesda, pp 363–452

    Google Scholar 

  • Killgore KJ, Hoover JJ (2001) Effects of hypoxia on fish assemblages in a vegetated waterbody. J Aquat Plant Manag 36:40–44

    Google Scholar 

  • Killgore KJ, Morgan RP II, Rybicki NB (1989) Distribution and abundance of fishes associated with submersed aquatic plants in the Potomac River. N Am J Fish Manag 9:101–111

    Article  Google Scholar 

  • Kimball ME, Able KW, Grothues TM (2010) Evaluation of long-term response of intertidal creek nekton to Phragmites australis (Common reed) removal in oligohaline Delaware Bay salt marsh. Restor Ecol 18:772–779

    Article  Google Scholar 

  • King AJ, Crook DA (2002) Evaluation of a sweep net electrofishing method for the collection of small fish and shrimp in lotic freshwater environments. Hydrobiologia 472:223–233

    Article  Google Scholar 

  • Kjelson MA, Turner WR, Johnson GN (1975) Description of a stationary drop-net for estimating nekton abundance in shallow waters. Trans Am Fish Soc 104:46–49

    Article  Google Scholar 

  • Klein Breteler JGP, Raat AJP, Grimm MP (1990) Efficiency and selectivity in fishing with electricity. In: Cowx I (ed) Developments in electric fishing. Fishing News Books, Oxford, pp 219–228

    Google Scholar 

  • Kneib RT (1984) Patterns in the utilization of the intertidal salt marsh by larvae and juveniles of Fundulus heteroclitus (Linnaeus) and Fundulus luciae (Baird). J Exp Mar Biol Ecol 83:41–51

    Article  Google Scholar 

  • Kneib RT (1991) Flume weir for quantitative collection of nekton from vegetated intertidal habitats. Mar Ecol Prog Ser 75:29–38

    Article  Google Scholar 

  • Kneib RT (1997) The role of tidal marshes in the ecology of estuarine nekton. Oceanogr Mar Biol Ann Rev 35:163–220

    Google Scholar 

  • Knight JG, Bain MB (1996) Sampling fish assemblages in forested floodplain wetlands. Ecol Freshw Fish 5:76–85

    Article  Google Scholar 

  • Koenig CC, Coleman FC (1998) Absolute abundance and survival of juvenile gags in sea grass beds of the northeastern Gulf of Mexico. Trans Am Fish Soc 127:44–55

    Article  Google Scholar 

  • Kohler CC, Ney JJ, Nigro AA (1979) Compact, portable vertical gill net system. Prog Fish-Cult 41:34–35

    Article  Google Scholar 

  • Kraft CE, Johnson BL (1992) Fyke-net and gill-net size selectivities for yellow perch in Green Bay, Lake Michigan. N Am J Fish Manag 12:230–236

    Article  Google Scholar 

  • Krebs CJ (1999) Ecological methodology, 2nd edn. Addison-Wesley Education Publishers, Inc., Menlo Park

    Google Scholar 

  • Krueger KL, Hubert WA, Price RM (1998) Tandem-set fyke nets for sampling benthic fishes in lakes. N Am J Fish Manag 18:154–160

    Article  Google Scholar 

  • Kushlan JA (1974) Quantitative sampling of fish populations in shallow, freshwater environments. Trans Am Fish Soc 103:348–352

    Article  Google Scholar 

  • Kushlan JA (1981) Sampling characteristics of enclosure fish traps. Trans Am Fish Soc 110:557–562

    Article  Google Scholar 

  • Kwak TJ (1988) Lateral movement and use of floodplain habitat by fishes of the Kankakee River, Illinois. Am Midl Nat 120:241–249

    Article  Google Scholar 

  • La Peyre MK, Birdsong T (2008) Physical variation of non-vegetated marsh edge habitats, and use patterns by nekton in Barataria Bay, Louisiana, USA. Mar Ecol Prog Ser 356:51–61

    Article  Google Scholar 

  • Laarman PW, Ryckman JR (1982) Relative size selectivity of trap nets for eight species of fish. N Am J Fish Manag 2:33–37

    Article  Google Scholar 

  • Laffaille P, Feunteun E, Lefeuvre J-C (2000) Composition of fish communities in a European macrotidal salt marsh (the Mont Saint-Michel Bay, France). Estuar Coast Shelf Sci 51:429–438

    Article  Google Scholar 

  • Lagler KF (1956) Freshwater fishery biology. Wm. C. Brown Publishers, Dubuque, p 421

    Google Scholar 

  • Lagler KF (1978) Capture, sampling, and examination of fishes. In: Bagwell T (ed) Methods for assessment of fish production in fresh waters. Blackwell Scientific Publications, Oxford

    Google Scholar 

  • Lapointe NWR, Corkum LD, Mandrak NE (2006) Point sampling by boat electrofishing: a test of the effort required to assess fish communities. N Am J Fish Manag 26:793–799

    Article  Google Scholar 

  • Larson EW, Johnson DL, Lych WE Jr (1986) A buoyant pop net for accurately sampling fish at artificial habitat structures. Trans Am Fish Soc 115:351–355

    Article  Google Scholar 

  • Layman CA, Smith DE (2001) Sampling bias of minnow traps in shallow aquatic habitats on the eastern shore of Virginia. Wetlands 21:145–154

    Article  Google Scholar 

  • Le Pape O, Chauvet F, Mahévas S, Lazure P, Guérault D, Désaunay (2003) Quantitative description of habitat suitability for the juvenile common sole (Solea solea L.) in the Bay of Biscay (France) and the contribution of different habitats to the adult population. J Sea Res 50:139–149

    Article  Google Scholar 

  • Legendre P, Legendre L (1998) Numerical ecology, second English edition. Developments in environmental modelling 20. Elsevier Science B.V, Amsterdam, p 854

    Google Scholar 

  • Leslie JK, Timmins CA (1992) Enhancement of ecological studies of freshwater larval fish: shore sampling. J Appl Ichthyol 8:214–221

    Article  Google Scholar 

  • Lester NP, Bailey PE, Hubert WA (2009) Coldwater fish in small standing waters. In: Bonar SA, Hubert WA, Willis DA (eds) Standard methods for sampling North American freshwater fishes. American Fisheries Society, Bethesda, pp 85–96

    Google Scholar 

  • Lewis III RR, Gilmore RG (2007) Important considerations to achieve successful mangrove forest restoration with optimum fish habitat. Bull Mar Sci 80(3):823–837

    Google Scholar 

  • Ley JA, McIvor CC, Montague CL (1999) Fishes in mangrove prop-root habitats of northeastern Florida Bay: distinct assemblages across an estuarine gradient. Estuar Coast Shelf Sci 48:701–723

    Article  Google Scholar 

  • Lin H-H, Shao K-T, Chiou W-L, Maa C-JW, Hsieh H-L, Wu W-L, Severinghaus LL, Wang Y-T (2003) Biotic communities of freshwater marshes and mangroves in relation to saltwater incursions: implications for wetland restoration. Biodivers Conserv 12:647–665

    Article  Google Scholar 

  • Loftus WF, Eklund A-M (1994) Long-term dynamics of an Everglades small fish assemblage. In: Davis S, Ogden JC (eds) Everglades: the system and its restoration. St. Lucie Press, Delray Beach, pp 461–483

    Google Scholar 

  • Lorenz JJ, Serafy JE (2006) Subtropical wetland fish assemblages and changing salinity regimes; implications for Everglades restoration. Hydrobiologia 569:401–422

    Article  Google Scholar 

  • Lorenz JJ, McIvor CC, Powell GVN, Frederick PC (1997) A drop net and removable walkway used to quantitatively sample fishes over wetland surfaces in the dwarf mangrove of the southern Everglades. Wetlands 17:346–359

    Article  Google Scholar 

  • Lougheed VL, Brosbie B, Chow-Fraser P (2001) Primary determinants of macrophyte community structure in 62 marshes across the Great Lakes basin: latitude, land use, and water quality effects. Can J Fish Aquat Sci 58:1603–1612

    Article  Google Scholar 

  • Lowe-McConnell RH (1987) Ecological studies in tropical fish communities. Cambridge University Press, Cambridge, p 382

    Book  Google Scholar 

  • Lyons J (1986) Capture efficiency of a beach seine for seven freshwater fishes in a north-temperate lake. N Am J Fish Manag 6:288–289

    Article  Google Scholar 

  • Macauley JM, Summers JK, Engle VD (1999) Estimating the ecological condition of the estuaries of the Gulf of Mexico. Environ Monit Assess 57:59–83

    Article  Google Scholar 

  • MacKenzie RA, Dionne M (2008) Habitat heterogeneity: importance of salt marsh pools and high marsh surfaces to fish production in two Gulf of Maine salt marshes. Mar Ecol Prog Ser 368:217–220

    Article  Google Scholar 

  • Magnuson JJ, Beckel AL, Mills K, Brant SB (1985) Surviving winter hypoxia: behavioral adaptations of fishes in a northern Wisconsin winterkill lake. Environ Biol Fish 14:241–250

    Article  Google Scholar 

  • Main MB, Ceilley DW, Stansly P (2007) Freshwater fish assemblages in isolated south Florida wetlands. Southeast Nat 6:343–350

    Article  Google Scholar 

  • Malavasi S, Georgalas V, Mainardi D, Torricelli P (2008) Antipredator response to overhead fright stimuli in hatchery-reared and wild European sea Bass (Dicentrarchus labrax L.) juveniles. Aquacult Res 39:276–282

    Article  Google Scholar 

  • Manson RA, Lonegran NR, Skilleter GA, Phinn SR (2005) An evaluation of the evidence for linkages between mangroves and fisheries: a synthesis of the literature and identification of research directions. Oceanogr Mar Biol 43:483–513

    Google Scholar 

  • Martinez PJ, Kolz AJ (2009) Evaluating the power output of the Smith-Root GPP 5.0 electrofisher to promote electrofishing fleet standardization. N Am J Fish Manag 29:570–575

    Article  Google Scholar 

  • Martinho F, Viegas I, Dolbeth M, Leitão R, Cabral HN, Pardal MA (2008) Assessing estuarine environmental quality using fish-based indices: performance evaluation under climatic instability. Mar Pollut Bull 56:1834–1843

    Article  PubMed  CAS  Google Scholar 

  • Mason CE, Blocker HD (1973) A stabilized drop trap for unit-area sampling of insects in short vegetation. Environ Entomol 2:214–216

    Google Scholar 

  • Matsuoka T, Nakashima T, Nagasawa N (2005) A review of ghost fishing: scientific approaches to evaluation and solutions. Fish Sci 71:691–702

    Article  CAS  Google Scholar 

  • McIvor CC, Odum WE (1986) The flume net: a quantitative method for sampling fishes and macrocrustaceans on tidal marsh surfaces. Estuaries 9:2190224

    Article  Google Scholar 

  • McIvor CC, Odum WE (1988) Food, predation risk, and microhabitat selection in a marsh fish assemblage. Ecology 69:1341–1351

    Article  Google Scholar 

  • McIvor CC, Silverman NL (2010) Modifications to the bottomless lift net for sampling nekton in tidal mangrove forests. Wetl Ecol Manag 18:627–635

    Article  Google Scholar 

  • McKenzie DI (2005) What are the issues with presence/absence data for wildlife managers. J Wildl Manag 69:849–860

    Article  Google Scholar 

  • McKenzie DI, Kendall WK (2002) How should detection probability be incorporated into estimates of relative abundance. Ecology 83:2387–2393

    Article  Google Scholar 

  • McKenzie DI, Nichols JD, Royle JA, Pollock KH, Bailey LL, Hines JE (2006) Occupancy estimation and modeling. Academic, San Diego

    Google Scholar 

  • McNeil DG, Closs GP (2007) Behavioral responses of a south-east Australian floodplain fish community to gradual hypoxia. Freshw Biol 52:412–420

    Article  CAS  Google Scholar 

  • Mendoza-Carranza M, Hoeinghaus DJ, Garcia AM, Romero-Rodriguez A (2010) Aquatic food webs in mangrove and seagrass habitats of Centla Wetland, a biosphere reserve in southeastern Mexico. Neotrop Ichthyol 8:171–178

    Article  Google Scholar 

  • Meng L, Orphanides DC, Powell JC (2002) Use of a fish index to assess habitat quality in Narragansett Bay, Rhode Island. Trans Am Fish Soc 131:731–742

    Article  Google Scholar 

  • Metzger RJ, Shafland PL (1986) Use of detonating cord for sampling fish. N Am J Fish Manag 6:113–118

    Article  Google Scholar 

  • Meynecke J-O, Lee SY, Duke NC (2008a) Linking spatial metrics and fish catch reveals the importance of coastal wetland connectivity to inshore fisheries in Queensland, Australia. Biol Conserv 141:981–996

    Article  Google Scholar 

  • Meynecke J-O, Poole GC, Werry J, Lee SY (2008b) Use of pit tags and underwater video recording in assessing estuarine fish movement in a high intertidal mangrove and salt marsh creek. Estuar Coast Shelf Sci 79:168–178

    Article  Google Scholar 

  • Millar RB, Fryer RJ (1999) Estimating the size-selection curves of towed gears, traps, nets, and hooks. Rev Fish Biol Fish 9:89–116

    Article  Google Scholar 

  • Miller C, Guillory V (1980) A comparison of marsh fish communities using the Wegener ring. Proc Ann Conf SE Assoc Fish Wildl Agencies 34:223–233

    Google Scholar 

  • Milliken GA, Johnson DE (2002) Analysis of messy data, vol III. Analysis of covariance. Chapman & Hall/CRC Press, Boca Raton

    Google Scholar 

  • Milliken GA, Johnson DE (2009) Analysis of messy data, vol I. Designed experiments, 2nd edn. Analysis of covariance. Chapman & Hall/CRC Press, Boca Raton

    Book  Google Scholar 

  • Miranda LE, Kidwell RH (2010) Unintended effects of electrofishing on nongame species. Trans Am Fish Soc 139:1315–1321

    Article  Google Scholar 

  • Miranda LE, Pugh LL (1997) Relationships between vegetation coverage and abundance, sex, and diet of juvenile largemouth bass during winter. N Am J Fish Manag 117:601–610

    Article  Google Scholar 

  • Mitsch WJ, Gosselink JG (2007) Wetlands, 4th edn. Wiley, New York

    Google Scholar 

  • Monzyk FR, Kelso WE, Rutherford DA (1997) Characteristics of woody cover used by brown madtoms and pirate perch in coastal plain streams. Trans Am Fish Soc 126:665–675

    Article  Google Scholar 

  • Mosepele K, Moyle PB, Merron GS, Purkey DR, Mosepele B (2009) Fish, floods, and ecosystem engineers: aquatic conservation in the Okavango Delta, Botswana. Bioscience 59:53–64

    Article  Google Scholar 

  • Mourning TE, Fausch KD, Gowan C (1994) Comparison of visible implant tags and Floy anchor tags on hatchery rainbow trout. N Am J Fish Manag 14:636–642

    Article  Google Scholar 

  • Mueller KW (2003) A comparison of electrofishing and scuba diving techniques to sample black bass in western Wisconsin lakes. N Am J Fish Manag 23:632–639

    Article  Google Scholar 

  • Mueller RP, Brown RS, Hop H, Moulton L (2006) Video and acoustic camera techniques for studying fish under ice: a review and comparison. Rev Fish Biol Fish 16:213–226

    Article  Google Scholar 

  • Mullins MA, Pierce BA, Gutzwiller KJ (2004) Assessment of quantitative enclosure sampling of larval amphibians. J Herpetol 38:166–172

    Article  Google Scholar 

  • Nagelkerken I, van der Velde G (2002) Do non-estuarine mangroves harbour higher densities of juvenile fish than adjacent shallow-water and coral reef habitats in Curaçao (Netherlands Antilles)? Mar Ecol Prog Ser 245:191–204

    Article  Google Scholar 

  • Newcomb TJ, Orth DJ, Stauffer DF (2007) Habitat evaluation. In: Guy CS, Brown ML (eds) Analysis and interpretation of freshwater fisheries data. American Fisheries Society, Bethesda, pp 843–886

    Google Scholar 

  • Nieland DL, Thomas RG, Wilson CA (2002) Age, growth, and reproduction of spotted seatrout in Barataria Bay, Louisiana. Trans Am Fish Soc 131:245–259

    Article  Google Scholar 

  • Nijboer RC, Schmidt-Kloiber A (2004) The effect of excluding taxa with low abundances or taxa with small distribution ranges on ecological assessment. Hydrobiologia 516:347–363

    Article  Google Scholar 

  • Niles JM, Hartman KJ (2007) Comparison of three larval fish gears to sample shallow water sites on a navigable river. N Am J Fish Manag 27:1126–1138

    Article  Google Scholar 

  • Obaza A, DeAngelis DL, Trexler JC (2011) Using data from an encounter sampler to model fish dispersal. J Fish Biol 78:495–513

    Article  PubMed  CAS  Google Scholar 

  • Paradis Y, Mingelbier M, Brodeur P, Magnan P (2008) Comparisons of catch and precision of pop nets, push nets, and seines for sampling larval and juvenile yellow perch. N Am J Fish Manag 28:1554–1562

    Article  Google Scholar 

  • Parsley MJ, Palmer DE, Burkhardt RW (1989) Variation in capture efficiency of a beach seine for small fishes. N Am J Fish Manag 9:239–244

    Article  Google Scholar 

  • Paukert CP, Willis DW (2002) Seasonal and diel habitat selection by bluegills in a shallow natural lake. Trans Am Fish Soc 131:1131–1139

    Article  Google Scholar 

  • Peoples BK, Frimpong EA (2011) Among-pass, interregional, and single versus multiple-season comparisons of detection probabilities of stream fishes. Trans Am Fish Soc 140:67–83

    Google Scholar 

  • Perrow MR, Jowitt AJD, Gonzalez Z (1996) Sampling fish communities in shallow lowland lakes: point-sample electric fishing vs electric fishing within stop-nets. Fish Manag Ecol 3:303–313

    Article  Google Scholar 

  • Petering RW, Johnson DL (1991) Distribution of fish larvae among artificial vegetation in a diked Lake Erie wetland. Wetlands 11:123–138

    Article  Google Scholar 

  • Peterson GW, Turner RE (1994) The value of salt marsh edge vs interior as habitat for fish and decapod crustaceans in a Louisiana tidal marsh. Estuaries 17:235–262

    Article  Google Scholar 

  • Piazza BP, La Peyre MK (2009) The effect of Hurricane Katrina on nekton communities of Breton Sound, Louisiana, USA. Estuar Coast Shelf Sci 83:97–104

    Article  Google Scholar 

  • Pierce CL, Corcoran AM, Gronbach AN, Hsia S, Mullarkey BJ, Schwartzhoff AJ (2001) Influence of diel period on electrofishing and beach seining assessments of littoral fish assemblages. N Am J Fish Manag 21:918–926

    Article  Google Scholar 

  • Pine WE, Hightower JE, Coggins LG, Lauretta MV, Pollock KH (2012) Design and analysis of tagging studies. In: Zale AV, Parrish DL, Sutton TM (eds) Fisheries techniques, 3rd edn. American Fisheries Society, Bethesda, pp 521–572

    Google Scholar 

  • Plunket JT, La Peyre M (2005) Comparison of finfish assemblage at clutched shell bottoms and mud bottoms in Barataria Bay, Louisiana. Bull Mar Sci 77:155–164

    Google Scholar 

  • Poff NL (1997) Landscape filters and species traits: toward mechanistic understanding and prediction in stream ecology. J N Am Bentholl Soc 16:391–409

    Article  Google Scholar 

  • Poizat G, Crivelli AJ (1997) Use of seasonally flooded marshes by fish in a Mediterranean wetland: timing and demographic consequences. J Fish Biol 51:106–119

    Article  PubMed  Google Scholar 

  • Pollock MS, Clarke LMJ, Dube MG (2007) The effects of hypoxia on fishes: from ecological relevance to physiological effects. Environ Rev 15:1–14

    Article  CAS  Google Scholar 

  • Pope KL, Kruse CG (2007) Condition. In: Guy CS, Brown ML (eds) Analysis and interpretation of freshwater fisheries data. American Fisheries Society, Bethesda, pp 423–472

    Google Scholar 

  • Pope JA, Margetts AR, Hamley JM, Okyuz EK (1975) Manual for methods for fish stock assessment Part 3: selectivity of fishing gear. FAO Fisheries technical paper 41

    Google Scholar 

  • Pope KL, Neumann RM, Bryan SD (2009) Warmwater fish in small standing waters. In: Bonar SA, Hubert WA, Willis DA (eds) Standard methods for sampling North American freshwater fishes. American Fisheries Society, Bethesda, pp 13–26

    Google Scholar 

  • Prado AL, Heckman CW, Martins FR (1994) The seasonal succession of biotic communities in wetlands of the tropical wet-and-dry climate zone: II. The aquatic macrophyte vegetation in the Pantanal of Mato Grosso, Brazil. Int Rev Ges Hydrobiol 79:569–589

    Article  Google Scholar 

  • Prchalova M, Kubecka J, Riha M, Litvin R, Cech M, Frouzova J, Hladik M, Hohausova E, Peterka J, Vasek M (2008) Overestimation of percid fishes (Percidae) in gillnet sampling. Fish Res 91:79–87

    Article  Google Scholar 

  • Professional Safety Committee (2008) Fisheries safety handbook. American Fisheries Society, Bethesda, p 48

    Google Scholar 

  • Pugh LL, Schramm HL Jr (1998) Comparison of electrofishing and hoopnetting in lotic habitats of the lower Mississippi River. N Am J Fish Manag 18:649–656

    Article  Google Scholar 

  • Rabeni CF, Lyon J, Mercado-Silva N, Peterson JT (2009) Warmwater fish in wadeable streams. In: Bonar SA, Hubert WA, Willis DW (eds) Standard methods for sampling North American freshwater fishes. American Fisheries Society, Bethesda, pp 43–58

    Google Scholar 

  • Rahel FJ (1984) Factors structuring fish assemblages along a bog lake successional gradient. Ecology 65:1276–1289

    Article  Google Scholar 

  • Rakocinski CF, Baltz DM, Fleeger JW (1992) Correspondence between environmental gradients and the community structure of marsh-edge fishes in a Louisiana estuary. Mar Ecol Prog Ser 80:135–148

    Article  Google Scholar 

  • Ramsey CW (1968) A drop-net deer trap. J Wildl Manag 32:187–190

    Article  Google Scholar 

  • Rehage JS, Loftus WF (2007) Seasonal fish community variation in headwater mangrove creeks in the southeastern Everglades: an examination of their role as dry-down refuges. Bull Mar Sci 80:625–645

    Google Scholar 

  • Reiss H, Kröncke I, Enrich S (2006) Estimating the catching efficiency of a 2-m beam trawl for sampling epifauna by removal experiments. ICES J Mar Sci 63:1453–1464

    Article  Google Scholar 

  • Reynolds JB, Kolz AL (2012) Electrofishing. In: Zale AV, Parrish DL, Sutton TM (eds) Fisheries techniques, 3rd edn. American Fisheries Society, Bethesda, pp 305–362

    Google Scholar 

  • Roegner GC, Dawley EW, Russell M, Whiting A, Teel DJ (2010) Juvenile salmonid use of reconnected tidal freshwater wetlands in Grays River, Lower Columbia River Basin. Trans Am Fish Soc 139:1211–1232

    Article  Google Scholar 

  • Rogers KB, White GC (2007) Analysis of movement and habitat use from telemetry data. In: Guy CS, Brown ML (eds) Analysis and interpretation of freshwater fisheries data. American Fisheries Society, Bethesda, pp 625–676

    Google Scholar 

  • Rolon AS, Maltchik L (2006) Environmental factors as predictors of aquatic macrophyte richness and composition in wetlands of southern Brazil. Hydrobiologia 556:221–231

    Article  CAS  Google Scholar 

  • Ross ST (2001) The inland fishes of Mississippi. University Press of Mississippi, Jackson

    Google Scholar 

  • Ross MJ, McCormick JH (1981) Effects of external radio transmitters on fish. Prog Fish Cult 43:67–72

    Article  Google Scholar 

  • Roth A-MF, Baltz DM (2009) Short-term effects of an oil spill on marsh edge fishes and decapod crustaceans. Estuar Coast 32:565–572

    Article  Google Scholar 

  • Rotherham D, Broadhurst MK, Gray CA, Johnson DD (2008) Developing a beam trawl for sampling estuarine fish and crustaceans: assessment of a codend cover and effects of different sizes of mesh in the body and codend. ICES Mar Sci 65:687–696

    Article  Google Scholar 

  • Rountree RA, Able KW (1992) Foraging habits, growth, and temporal patterns of salt-marsh creek habitat use by young-of-the-year summer flounder in New Jersey. Trans Am Fish Soc 121:756–776

    Article  Google Scholar 

  • Rowe DK, Taumpoepeau A (2004) Decline of common smelt (Retropinna retropinna) in turbid, eutrophic lakes in the North Island of New Zealand. Hydrobiologia 523:149–158

    Article  Google Scholar 

  • Rozas LP (1992) Bottomless lift net for quantitatively sampling nekton on intertidal marshes. Mar Ecol Prog Ser 89:287–292

    Article  Google Scholar 

  • Rozas LP, Minello TJ (1997) Estimating densities of small fishes and decapod crustaceans in shallow estuarine habitats: a review of sampling design with focus on gear selection. Estuaries 20:199–213

    Article  Google Scholar 

  • Rozas LP, Odum WE (1987a) Fish and macrocrustacean use of submerged plan beds in tidal freshwater marsh creeks. Mar Ecol Prog Ser 38:101–108

    Article  Google Scholar 

  • Rozas LP, Odum WE (1987b) The role of submerged aquatic vegetation in influencing the abundance of nekton on contiguous tidal fresh-water marshes. J Exp Mar Biol Ecol 114:289–300

    Article  Google Scholar 

  • Rozas LP, Odum WE (1987c) Use of tidal freshwater marshes by fishes and macrofaunal crustaceans along a marsh stream-order gradient. Estuaries 10:36–43

    Article  Google Scholar 

  • Rozas LP, Reed DJ (1994) Comparing nekton assemblages of subtidal habitats in pipeline canals traversing brackish and saline marshes in coastal Louisiana. Wetlands 14:262–275

    Article  Google Scholar 

  • Rudstam LG, Magnuson JJ, Tonn WM (1984) Size selectivity of passive fishing gear: a correction for encounter probability applied to gill nets. Can J Fish Aquat Sci 41:1252–1255

    Article  Google Scholar 

  • Rudstam LG, Jech JM, Parker-Stetter SL, Horne JK, Sullivan PJ, Mason DM (2012) Fisheries acoustics. In: Zale AV, Parrish DL, Sutton TM (eds) Fisheries techniques, 3rd edn. American Fisheries Society, Bethesda, pp 597–636

    Google Scholar 

  • Ruetz CR III, Uzarski DG, Krueger DM, Rutherford ES (2007) Sampling a littoral fish assemblage: comparison of small-mesh fyke netting and boat electrofishing. N Am J Fish Manag 27:825–831

    Article  Google Scholar 

  • Rulifson RA (1991) Finfish utilization of man-initiated and adjacent natural creeks of South Creek Estuary, North Carolina suing multiple gear types. Estuaries 14:447–464

    Article  Google Scholar 

  • Rutherford DA, Gelwicks KR, Kelso WE (2001) Physicochemical effects of the flood pulse on the fishes in the Atchafalaya River basin, Louisiana. Trans Am Fish Soc 130:276–288

    Article  Google Scholar 

  • Sabo MJ, Bryan CF, Kelso WE, Rutherford DA (1999) Hydrology and aquatic habitat characteristics of a riverine swamp: II. Hydrology and the occurrence of chronic hypoxia. Reg Riv Res Manag 15:525–544

    Article  Google Scholar 

  • Saint-Paul U, Zuanon J, Correa MAV, Garcia M, Fabre NN, Berger U, Junk WJ (2000) Fish communities in central Amazonian white- and blackwater floodplains. Environ Biol Fish 57:235–250

    Article  Google Scholar 

  • Savino JF, Stein RA (1989) Behavioral interactions between fish predators and their prey: effects of plant density. Anim Behav 37:311–321

    Article  Google Scholar 

  • Scheerer PD (2002) Implications of floodplain isolation and connectivity on the conservation of an endangered minnow, Oregon chub, in the Williamette River, Oregon. Trans Am Fish Soc 131:1070–1080

    Article  Google Scholar 

  • Scheidegger KJ, Bain MB (1995) Larval fish distribution and microhabitat use in free-flowing and regulated rivers. Copeia 1995:125–135

    Article  Google Scholar 

  • Scheirer JW, Coble DW (1991) Effect of Floy FD-67 anchor tags on growth and condition of northern pike. N Am J Fish Manag 11:369–373

    Article  Google Scholar 

  • Schneider KN, Winemiller KO (2008) Structural complexity of woody debris patches influences fish and macroinvertebrate species richness in a temperate floodplain-river system. Hydrobiologia 610:235–244

    Article  Google Scholar 

  • Scholten M (2003) Efficiency of point abundance sampling by electro-fishing modified for short fishes. J Appl Ichthyol 19:265–277

    Article  Google Scholar 

  • Schrage LJ, Downing JA (2004) Pathways of increased water clarity after fish removal from Ventura marsh; a shallow, eutrophic wetland. Hydrobiologia 511:215–231

    Article  Google Scholar 

  • Searcy SP, Sponaugle S (2001) Selective mortality during the larval-juvenile transition in two coral reef fishes. Ecology 82:2452–2470

    Google Scholar 

  • Seilheimer TS, Chow-Fraser P (2006) Development and use of the Wetland Fish Index to assess the quality of coastal wetlands in the Laurentian Great Lakes. Can J Fish Aquat Sci 63:354–366

    Article  CAS  Google Scholar 

  • Seilheimer TS, Chow-Fraser P (2007) Application of the Wetland Fish Index to northern Great Lakes marshes with emphasis on Georgian Bay coastal wetlands. J Great Lakes Res 33:154–171

    Article  Google Scholar 

  • Seilheimer TS, Mahoney TP, Chow-Fraser P (2009) Comparative study of ecological indices for assessing human-induced disturbance in coastal wetlands of the Laurentian Great Lakes. Ecol Indic 9:81–91

    Article  Google Scholar 

  • Selleslagh J, Amara R (2008) Environmental factors structuring fish composition and assemblages in a small macrotidal estuary (eastern English Channel). Estuar Coast Shelf Sci 79:507–517

    Article  Google Scholar 

  • Serafy JE, Harrell RM, Stevenson JC (1988) Quantitative sampling of small fishes in dense vegetation: design and field testing of portable “pop-nets. J Appl Ichthyol 4:149–157

    Article  Google Scholar 

  • Sheaves M, Johnston R (2008) Influence of marine and freshwater connectivity on the dynamics of subtropical estuarine wetland fish metapopulations. Mar Ecol Prog Ser 357:225–243

    Article  Google Scholar 

  • Sheftall IV, WL (2011) Factors structuring zooplankton density and composition within a Louisiana river and floodplain tributaries with emphasis on hydrologic processes. MS thesis. Louisiana State University, Baton Rouge

    Google Scholar 

  • Shervette VR, Aguirre WE, Blacio E, Cevallos R, Gonzalez M, Pozo F, Gelwick F (2007) Fish communities of a disturbed mangrove wetland and an adjacent tidal river in Palmar, Ecuador. Estuar Coast Shelf 72:115–128

    Article  Google Scholar 

  • Shilling F, White A, Lippert L, Lubell M (2010) Contaminated fish consumption in California’s Central Valley Delta. Environ Res 110:334–344

    Article  PubMed  CAS  Google Scholar 

  • Shono H (2008) Application of the Tweedie distribution to zero-catch data in CPUE analysis. Fish Res 93:154–162

    Article  Google Scholar 

  • Smith PE, Counts C, Clutter RI (1968) Changes in filtering efficiency of plankton nets due to clogging under tow. ICES Mar Sci 32:232–248

    Article  Google Scholar 

  • Snodgrass JW, Bryan AL, Lide RF, Smith GM (1996) Factors affecting the occurrence and structure of fish assemblages in isolated wetlands of the upper coastal plain, USA. Can J Fish Aquat Sci 53:443–454

    Article  Google Scholar 

  • Snyder DE (2003) Invited overview: conclusions from a review of electrofishing and its harmful effects on fish. Rev Fish Biol Fish 13:445–453

    Article  Google Scholar 

  • Songur A, Ozan OA, Sarsilmaz M (2010) The toxic of formaldehyde on the nervous system. Rev Environ Contam Toxicol 203:105–118

    Article  PubMed  CAS  Google Scholar 

  • Steele MA, Schroetter SC, Page HM (2006) Sampling characteristics and biases of enclosure traps for sampling fishes in estuaries. Estuar Coast 29:630–638

    Google Scholar 

  • Steinhorst RK, Samuel MD (1989) Sightability adjustment methods for aerial surveys of wildlife populations. Biometrics 45:415–425

    Article  Google Scholar 

  • Stoner AW, Ryer CH, Parker SJ, Auster PJ, Wakefield WW (2008) Evaluating the role of fish behavior in surveys conducted with underwater vehicles. Can J Fish Aquat Sci 65:1230–1243

    Article  Google Scholar 

  • Streever WJ, Crisman TL (1993) A comparison of fish populations from natural and constructed freshwater marshes in central Florida. J Freshw Ecol 8:149–153

    Article  Google Scholar 

  • Stunz GW, Minello TJ, Rozas (2010) Relative value of oyster reef as habitat for estuarine nekton in Galveston Bay, Texas. Mar Ecol Prog Ser 406:147–159

    Article  Google Scholar 

  • Suski CD, Ridgway MS (2009) Winter biology of centrarchid fishes. In: Cooke SJ, Philipp (eds) Centrarchid fishes: diversity, biology, and conservation. Blackwell-Wiley, Ames, pp 264–292

    Chapter  Google Scholar 

  • Sutton TM, Benson AC (2003) Influence of external transmitter shape and size on tag retention and growth of juvenile Lake Sturgeon. Trans Am Fish Soc 132:1257–1263

    Article  Google Scholar 

  • Swingle HS (1954) Fish populations in Alabama rivers and impoundments. Trans Am Fish Soc 83:47–57

    Article  Google Scholar 

  • Talbot CW, Able KW (1984) Composition and distribution of larval fishes in New Jersey high marshes. Estuaries 7:434–443

    Article  Google Scholar 

  • Tátrai AS, Győrgy AI, Biro P (2008) Comparison of fish size distribution and fish abundance estimates obtained with hydroacoustics and gill netting in the open water of a large shallow lake. Ann Limnol Int J Lim 44:231–240

    Article  Google Scholar 

  • Teels BM, Mazanti LE, Rewa CA (2004) Using an IBI to assess effectiveness of mitigation measures to replace loss of a wetland-stream ecosystem. Wetlands 24:375–384

    Article  Google Scholar 

  • Thomaz SM, Bini LM, Bozelli RL (2007) Floods increase similarity among aquatic habitats in river-floodplain systems. Hydrobiologia 579:1–13

    Article  Google Scholar 

  • Thurow RF, Dolloff CA, Marsden JE (2012) Visual observation of fish and aquatic habitat. In: Zale AV, Parrish DL, Sutton TM (eds) Fisheries techniques, 3rd edn. American Fisheries Society, Bethesda, pp 781–818

    Google Scholar 

  • Tonn WM, Magnuson JJ (1982) Patterns in the species composition and richness of fish assemblages in northern Wisconsin lakes. Ecology 63:1149–1166

    Article  Google Scholar 

  • Trebitz AS, Brazner JC, Pearson MS, Peterson GS, Dk T, Taylor DL (2009a) Patterns in habitat and fish assemblages within Great Lakes coastal wetlands and implications for sampling design. Can J Fish Aquat Sci 66:1343–1354

    Article  Google Scholar 

  • Trebitz AS, Kelly JR, Hoffman JC, Peterson GS, West CW (2009b) Exploiting habitat and gear patterns for efficient detection of rare and non-native benthos and fish in Great Lakes coastal ecosystems. Aquat Invasions 4:651–667

    Article  Google Scholar 

  • Troutman JP, Rutherford DA, Kelso WE (2007) Patterns of habitat use among vegetation-dwelling littoral fishes in the Atchafalaya River basin, Louisiana. Trans Am Fish Soc 136:1063–1075

    Article  Google Scholar 

  • Tschernij V, Suuronen P, Jounela P (2004) A modeling approach for assessing short-term catch losses as a consequence of mesh size increase. Fish Res 69:399–406

    Article  Google Scholar 

  • Turner A, Trexler JC (1997) Sampling invertebrates from the Florida Everglades: a comparison of alternative methods. J N Am Bentholl Soc 16:694–709

    Article  Google Scholar 

  • Underwood AJ (1981) Techniques of analysis of variance in experimental marine biology and ecology. Oceanogr Mar Biol Annu Rev 19:513–605

    Google Scholar 

  • Underwood AJ, Chapman MG (2003) Power, precaution, Type II error and sampling design in the assessment of environmental impacts. J Exp Mar Biol Ecol 296:49–70

    Article  Google Scholar 

  • Unkenholz EG, Brown ML, Pope KL (1997) Oxytetracycline marking efficacy for yellow perch fingerlings and temporal assays of tissue residues. Prog Fish-Cult 59:280–284

    Article  Google Scholar 

  • Uzarski DG, Burton TM, Cooper MJ, Ingram JW, Timmermans STA (2005) Fish habitat use within and across wetland classes in coastal wetlands of the five Great Lakes: development of a fish-based Index of Biotic Integrity. J Great Lakes Res 31:171–187

    Article  Google Scholar 

  • Van Geest GJ, Wolters H, Roozen FCJM, Coops H, Roijackers RMM, Buijse AD, Scheffer M (2005) Water-level fluctuations affect macrophyte richness in floodplain lakes. Hydrobiologia 539:239–248

    Article  Google Scholar 

  • Varnell LM, Havens KJ (1995) A comparison of dimension-adjusted catch data methods for assessment of fish and crab abundance in intertidal salt marshes. Estuaries 18:319–325

    Article  Google Scholar 

  • Walker RE, Applegate RL (1976) Growth, food, and possible ecological effects of young-of-the-year walleye in a South Dakota prairie pothole. Prog Fish Cult 38:217–220

    Article  Google Scholar 

  • Waters TF, Knapp RJ (1961) An improved stream bottom fauna sampler. Trans Am Fish Soc 20:225–226

    Article  Google Scholar 

  • Webb GJW, Messel H (1977) Crocodile capture techniques. J Wildl Manag 41:572–575

    Article  Google Scholar 

  • Wegener W, Holcomb D, Williams V (1973) Sampling shallow water fish populations using the Wegener ring. Proc Ann Conf SE Assoc Fish Wildl Agencies 27:663–673

    Google Scholar 

  • Werner RG (1969) Ecology of limnetic bluegill (Lepomis macrochirus) fry in Crane Lake, Indiana. Am Midl Nat 81:164–181

    Article  Google Scholar 

  • West JM, Zedler JB (2000) Marsh-creek connectivity: fish use of a tidal salt marsh in southern California. Estuaries 23:699–710

    Article  Google Scholar 

  • Wharton DI (2005) Many zeros does not mean zero inflation: comparing the goodness-of-fit of parametric models to multivariate abundance data. Environmetrics 16:275–289

    Article  Google Scholar 

  • Wilcox DA, Whillans TH (1999) Techniques for restoration of disturbed coastal wetlands of the Great Lakes. Wetlands 19:835–857

    Article  Google Scholar 

  • Williams GD, Zedler JB (1999) Fish assemblage composition in constructed and natural tidal marshes of San Diego Bay: relative influence of channel morphology and restoration history. Estuaries 22:702–716

    Article  Google Scholar 

  • Wolski LF, Trexler JC, Nelson EB, Philippi T, Perry SA (2004) Assessing visitor impacts from long-term sampling of wetland communities in the Everglades. Freshw Biol 49:1381–1390

    Article  Google Scholar 

  • Woodward RT, Wui Y-S (2001) The economic value of wetland services: a meta-analysis. Ecol Econ 37:257–270

    Article  Google Scholar 

  • Yozzo DJ, Smith DE (1998) Composition and abundance of resident marsh-surface nekton: comparison between tidal freshwater and salt marshes in Virginia, USA. Hydrobiologia 362:9–19

    Article  Google Scholar 

  • Zimmerman RJ, Minello TJ, Zamora G Jr (1984) Selection of vegetated habitat by brown shrimp, Penaus aztecus, in a Galveston Bay salt marsh. Fish Bull 82:325–336

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Michael D. Kaller .

Editor information

Editors and Affiliations

Laboratory Activities and Problem Sets

Laboratory Activities and Problem Sets

In the following sections, we offer field and laboratory activities and additional exercises to illustrate topics discussed in this chapter. Note that field fish sampling may require authorization or notification of local regulatory agencies. Please adhere to your institution’s policies regarding animal care and use during these exercises.

6.1.1 Baited Versus Unbaited Traps

Goal: To determine the influence of bait type on potential sampling bias in minnow traps.

Overview: Passive sampling is quite popular for fisheries studies. However, biases may be introduced by gear type and method of deployment. This field or laboratory exercise examines biases that may occur as the result of sampling choices.

Supplies for field trip version: Minnow traps (≥6), bait (commercial fish food and commercial fish attractant such as Berkley trout bait), rope, stakes (equal to minnow traps), standard aquarium dip nets (1–2) buckets, sorting pans (2–3), fish identification guides such as Freshwater Fishes of Virginia (Jenkins and Burkhead 1994).

Supplies for laboratory version of experiment: Aquaria, no larger than 10 gal or 38 L (6), hardware cloth (fine mesh) fashioned into minnow traps (cylinder 7–10 cm in diameter, 15–20 cm long, with 5 cm, or other dimension less than the diameter, openings), bait (as above), standard aquarium dip nets.

6.1.1.1 Methods for Field Trip Version

The evening before the planned trip, minnow traps should be baited and deployed in a nearby wetland. At least two minnow traps should be used for each treatment: unbaited; baited with commercial fish food; and baited with commercial fish attractant. All six minnow traps should be secured by rope to stakes driven into the banks and deployed along the shoreline a sufficient depth to cover the trap. Deployment and retrieval times should be noted. Students should empty the contents of each trap into individual holding buckets or directly into sorting pans if few fish are caught. Students should then identify and enumerate fish and estimate catch per unit effort (CPUE) as the number of fish of each species in a trap divided by the number of hours deployed. Next, students should calculate the arithmetic mean CPUE for each of the three trap treatments and answer the questions below.

6.1.1.2 Methods for Laboratory Version

Instructor(s) will stock three aquaria with similar densities of one or more species of fish obtained from a local wetland, bait shop or pet store. Instructors or students should build small minnow traps prior to the experiment with narrow openings sufficient for fish entry. Two minnow traps will be deployed during the laboratory period in three aquarium treatments: (1) one trap with fish food and one with fish bait; (2) one trap with fish food and one with no bait; and (3) one with fish bait and one with no bait. Time of trap deployment into the aquaria should be noted. Students will observe fish movement into minnow traps and record the species and number of fish in each trap at the end of the laboratory period. CPUE will be estimated as the number of fish of each species in a trap divided by the number of minutes passed since the traps were placed into the aquaria (Hubert et al. 2012)

$$ \mathrm{ CPUE}={{{\sum {\left( {{{\mathrm{ n}}_1}+{{\mathrm{ n}}_2}+\ldots {{\mathrm{ n}}_{\mathrm{ i}}}} \right)} }} \left/ {{{{\mathrm{ t}}_{\mathrm{ i}}}}} \right.} $$

where n1 is the number of fish of the first species, n2 is the number of fish of the second species, ni is the number of fish in the last species, and ti in the number of minutes a trap was deployed. Students can calculate the arithmetic mean CPUE for each trap type (two traps each for commercial food, commercial bait, and unbaited). Students should then answer the questions below.

6.1.1.3 Questions for Reflection and Study

  1. 1.

    Which trap type exhibited the highest mean CPUE, combining all fish species that were collected? Did any single fish species differ from this pattern (i.e., did any species become trapped at a higher CPUE in another type of trap than the one that collected the most overall fish)? Did anything that you observed about the trap or bait suggest why CPUE was highest in this type of trap?

  2. 2.

    Do you believe that your experiment has evidence of trap bias? Did bait type matter? Explain and defend with your data.

  3. 3.

    Could your data be comparable with a minnow trap study that used another kind of bait? Why or why not?

  4. 4.

    Consult a regional fish guide, such as Freshwater Fishes of Virginia (Jenkins and Burkhead 1994), about life history and habitat requirements of the fish with the highest CPUE in each trap type. Does something about their life history or habitat requirements suggest why the fish was attracted to that trap type?

Jenkins RE, Burkhead NM (1994) Freshwater fishes of Virginia. American Fisheries Society, Bethesda, 1079 pp

6.1.2 Removal Sampling and the Influence of Increasing Sampling Effort

Goal: Introduce removal sampling and common estimators of population size associated with removal sampling.

Overview: In small, enclosed wetlands or wetlands where habitats may be segregated from the surrounding areas, researchers can use closed population methods to estimate fish population size. One historically popular method is population estimation by removal. In removal sampling, fish are collected and removed or held while additional fish are collected. A minimum of two collections are needed, and often additional collections are recommended because the additional collections enhance the population estimate. This experiment may be conducted in the field by seining or electrofishing, whichever is available, or by dip net in the laboratory.

Supplies needed for a field version: Seine or backpack electrofishing unit (depending on availability and suitability given local conductivity), gloves and waders, long-handled nets (electrofishing only), buckets or large cooler or fish basket to hold fish, block nets (if sampling a small area of a larger wetland).

Supplies needed for laboratory version: table top, simulated fish (e.g., small plastic vials or packing peanuts) and a sampling “net” (e.g., an inverted shoe box).

6.1.2.1 Methods for Field Version

A small, enclosed wetland should be selected or a small area within a larger wetland should be enclosed by block net. The ideal area would be about one-eight acre, if block nets are deployed. Students should conduct 10-m quantitative seine hauls (Fig. 6.1) or 100-m electrofishing passes (Fig. 6.3). Ideally, no fewer than four hauls or passes should be conducted; however, if very few fish are caught on the second and third haul or pass, the fourth haul or pass may be omitted. At the end of each haul or pass, fish should be identified and enumerated and then transferred to a holding bucket, cooler, or basket, until the final haul or pass when all fish can be returned to the wetland. Students should record the number and type of fish in each haul or pass to answer the questions in this section.

6.1.2.2 Methods for Laboratory Version

A small table top should be covered with random patches of “fish”, and the “sampler” should be given to a blindfolded student to randomly place on the table. After each sample is taken, the remaining “fish” should be collected and re-distributed on the table top. For best results, the sampler should probably be able to cover about 20 % of the table top. For each sample, students should record the number of “fish” and set them aside. After at least three samples, students should be able to answer the questions in this section.

6.1.2.3 Questions for Reflection and Study

The Zippin method is commonly used to estimate fish populations with two removals (Hayes et al. 2007). The Zippin method is a maximum likelihood method and differs from the regression based DeLurly method more frequently used in the past. The Zippin method assumes all fishes had equal vulnerability to being sampled by the selected gear, equal effort was expended for each sample, and the probability of capture (catchability) was equal for each sample. The Zippin method also requires that the first sample yield more fish than the second sample. The Zippin method is

$$ \mathrm{ N}\text{--}\mathrm{ hat}={{{\mathrm{ n}_1^2}} \left/ {{\left( {{{\mathrm{ n}}_1}-{{\mathrm{ n}}_2}} \right)}} \right.} $$

where N-hat is the estimate of the fish population, n1 is the number of fish removed in the first sample, and n2 is the number of fish removed in the second sample. When we estimate, we also desire to know the precision of the estimate. For the Zippin method, we can estimate the precision of the estimate by its variance

$$ \mathrm{ V}\left( \mathrm{ N} \right)={{{\mathrm{ n}_1^2\mathrm{ n}_2^2\left( {{{\mathrm{ n}}_1}+{{\mathrm{ n}}_2}} \right)}} \left/ {{{{{\left( {{{\mathrm{ n}}_1}-{{\mathrm{ n}}_2}} \right)}}^4}}} \right.} $$

where V(N) is the variance of the Zippin estimate, n1 is the number of fish removed in the first sample, and n2 is the number of fish removed in the second sample.

The Zippin method is not possible for more than two removals. For three removals, the following formula is used following Hayes et al. (2007) citing Junge and Libosvarksy (1965) as cited in Seber (1982)

$$ \mathrm{ N}\text{--}\mathrm{ hat}={{{6{{\mathrm{ X}}^2}-3\mathrm{ XY}-{{\mathrm{ Y}}^2}+\mathrm{ Y}\surd \left( {{{\mathrm{ Y}}^2}+6\mathrm{ XY}-3{{\mathrm{ X}}^2}} \right)}} \left/ {{18\left( {\mathrm{ X}-\mathrm{ Y}} \right)}} \right.} $$

where N-hat is the population estimate, \( \mathrm{ X}\ \mathrm{ is}\ 2{{\mathrm{ n}}_1}+{{\mathrm{ n}}_2} \) and \( \mathrm{ Y}\ \mathrm{ is}\ \mathrm{ n}{_1}+\mathrm{ n}{_2}+\mathrm{ n}{_3} \). Again, it is always of interest to estimate variance, which is estimated by finding q or catchability first as

$$ \mathrm{ q}\text{--}\mathrm{ hat}={{{3\mathrm{ X}-\mathrm{ Y}-\surd \left( {{{\mathrm{ Y}}^2}+6\mathrm{ XY}-3{{\mathrm{ X}}^2}} \right)}} \left/ {{2\mathrm{ X}}} \right.} $$

where q-hat is the catchability estimate, \( \mathrm{ X}\ \mathrm{ is}\ 2{{\mathrm{ n}}_1}+{{\mathrm{ n}}_2} \) and \( \mathrm{ Y}\ \mathrm{ is}\ \mathrm{ n}{_1}+\mathrm{ n}{_2}+\mathrm{ n}{_3} \). Then, we estimate variance as

$$ \mathrm{ V}\left( \mathrm{ N} \right)={{{\mathrm{ N}\text{--}\mathrm{ ha}\mathrm{ t}\left( {1-\mathrm{ q}\text{--}\mathrm{ ha}\mathrm{ t}} \right)\mathrm{ q}\text{--}\mathrm{ ha}\mathrm{ t}}} \left/ {{{{{\left( {1-\mathrm{ q}\text{--}\mathrm{ ha}\mathrm{ t}} \right)}}^2}-\left[ {\mathrm{ t}{{{\left( {1-\mathrm{ q}\text{--}\mathrm{ ha}\mathrm{ t}} \right)}}^2}\mathrm{ q}\text{--}\mathrm{ ha}{{\mathrm{ t}}^{{\left( {\mathrm{ t}-1} \right)}}}} \right]}} \right.} $$

where V(N) is the estimate of the variance of the fish population, q-hat is the estimate of catchability, and t is the number of removals.

  1. 1.

    Estimate the fish population size and variance by the Zippin method with the first two removals. Then estimate the fish population by the three removal method with the first, second, and third removals. Estimate catchability and the variance of the three removal population estimate.

    1. 1a

      Do the fish population estimates differ?

    2. 1b

      If smaller variance may be assumed to suggest greater precision, did adding another removal increase precision?

    3. 1c

      Given your experience sampling, do you think that adding another removal is worth the difference in precision?

    For the field version only:

    1. 1d

      Given that you do not know the actual number of fish present, do you believe that removal sampling provides a reasonable estimate of the fish present?

    2. 1e

      Can you get insights from the variance? Defend your answer with your data.

    For the laboratory version only:

    1. 1d

      Show your estimates to the instructor, who will reveal the actual number. Which estimate was closer to the real number?

    2. 1e

      Given your experiences, how confident are you that removal sampling may offer reasonable estimates of fish populations?

  1. 2.

    Another common assessment is to describe the taxonomic diversity of fishes in a wetland. One common and readily estimated measure of diversity is the Shannon index, also termed the Shannon-Wiener or Shannon-Weaver Index. The index ranges from a low end near one, which indicates low species richness (low number of species) and evenness (few species numerically dominate the community), to 3.5, which indicates high species richness (higher number of species) and evenness (numbers spread among the species). The Shannon Index is found by

    $$ {\mathrm{ H}}^{\prime}= - {\Sigma_{\mathrm{ i}}}^{\mathrm{ s}}\left[ {{{\mathrm{ p}}_{\mathrm{ i}}} \ln \left( {{{\mathrm{ p}}_{\mathrm{ i}}}} \right)} \right] $$

    where pi is the proportion of an individual species. For example, if 3 species are present in a sample at 35, 25, and 15 individuals, \( {\mathrm{ H}}^{\prime}=-\left\{ {\left[ \left( {35/75} \right) {\ln \left( {35/75} \right)} \right]+\left[ {\left( {25/75} \right) \ln \left( {25/75} \right)} \right]+\left[ {\left( {15/75} \right) \ln \left( {15/75} \right)} \right]} \right\}=-\left[ {\left( {-0.36} \right)+\left( {-0.37} \right)+\left( {-0.32} \right)} \right] = 1.05 \) suggesting low diversity of species and dominance by 1 species.

    1. 2a

      Estimate H’ for the first removal, then for the first 2 removals combined, and then for all removals combined.

    2. 2b

      Does adding removals increase H’? What does this mean?

    3. 2c

      Is H′ sensitive to the number of removals?

Hayes DB, Bence JR, Kwak TJ, Thompson BE (2007) Abundance, biomass, and production. In: Guy CS, Brown ML (eds) Analysis and interpretation of freshwater fisheries data. American Fisheries Society, Bethesda, pp 327–374

Junge CO, Libosvarsky J (1965) Effects of size selectivity on population estimates based on successive removals with electrofishing gears. Zoologicke Listy 14:171–178

Seber GAF (1982) The estimation of animal abundance and related parameters. Blackburn Press, Caldwell, , pp 672

6.1.3 Additional Exercises

  1. 1.

    Suppose a fish manager is tasked to sample a wetland in order to determine its ecological health. She assumes that a wetland with high fish diversity (a Shannon index above 2.5 for this small wetland) and high fish density (more than100 fish per acre) would indicate a healthy ecosystem. She conducts removal sampling by seine hauls in a 1-acre enclosed portion of the wetland. The hauls produced 56 fish, 32 fish, and 13 fish. The hauls produced 9 emerald shiners, 7 fathead minnows, 5 common carp, 9 largemouth bass, 4 bluegill, 7 pumpkinseed sunfish, 9 green sunfish, 3 sand shiners, 6 warmouth bass, 5 chain pickerels, 3 golden shiners, 9 Johnny darters, 9 white crappies, 5 brown bullheads, and 11 yellow bullheads. Use the estimators given in Sect. 6.4.3 to determine if the wetland would be considered healthy.

  2. 2.

    Suppose the same fish manager in question 1 visited a second wetland. This time, the hauls produced 39 fish, 41 fish, and 18 fish. Use the estimators given in Sect. 6.4.3 to determine if the wetland would be considered healthy. The hauls produced 19 emerald shiners, 7 fathead minnows, 5 common carp, 1 largemouth bass, 1 bluegill, 8 pumpkinseed sunfish, 19 green sunfish, 3 sand shiners, 3 warmouth, 2 chain pickerels, 3 golden shiners, 2 Johnny darters, 2 white crappies, 12 brown bullheads, and 11 yellow bullheads. Use the estimators given in Sect. 6.4.2 to determine if the wetland would be considered healthy.

  3. 3.

    A wetland manager decided to sample a large wetland with boat electrofishing and gill nets. The electrofishing sampled for 45 min and collected 100 fish of 7 species. The gill nets soaked for 12 h and collected 292 fish in 11 species. Which gear exhibited the higher CPUE? Why might the electrofishing have collected fewer species than the gill net?

  4. 4.

    A wetland manager sampled a boat-accessible wetland with point abundance electrofishing and a drop sampler. The point abundance electrofishing sampled 900 s in five 100 m2 areas surrounded by block nets, yielding 14, 25, 9, and five fish. The drop trap of 1 m2 was deployed 10 times yielding 1 fish, 0 fish, 3 fish, 0 fish, 0 fish, 1 fish, 0 fish, 0 fish, 0 fish, and 2 fish. Estimate fish density per 1 m2 for both methods. Which method estimated a higher mean fish density?

Rights and permissions

Reprints and permissions

Copyright information

© 2013 Springer Science+Business Media Dordrecht

About this chapter

Cite this chapter

Kaller, M.D., Kelso, W.E., Trexler, J.C. (2013). Wetland Fish Monitoring and Assessment. In: Anderson, J., Davis, C. (eds) Wetland Techniques. Springer, Dordrecht. https://doi.org/10.1007/978-94-007-6931-1_6

Download citation

Publish with us

Policies and ethics