density may vary with depth; therefore, sampling should be done at several depthsdetermined by the depth <strong>of</strong> the thermocline; the euphotic zone, if applicable; and overalldepth at the station. In shallow areas (one to two meters) subsurface samples (to a depth<strong>of</strong> one meter) are usually sufficient. In lentic environments, sample at one-meter intervalsfrom the surface to the lake bottom because these organisms are not confined to theeuphotic zone.Zooplankton analysis requires at least six liters in moderately and highly productivewaters. Sample size, preservation and storage are dependent upon certain variables. Referto the NJDEP Field Sampling Manual for details. Generally, freshwater samples forspecies composition analysis should be preserved with a solution <strong>of</strong> neutralized formalin(5 ml neutralized buffer with formalin/100 ml <strong>of</strong> sample). All preserved samples shouldbe stored in the dark immediately.When collecting live samples, leave at least a four-cm air space in the bottle and chill to4º C (e.g. in a cooler with ice) during transit storage. For delicate flagellated species, donot refrigerate sample bottles. Maintain in situ temperature by storing them out <strong>of</strong> directsunlight, in an ice chest, with some <strong>of</strong> the ambient water. Surface samples in streams,rivers, shallow estuaries and coastal water can be collected simply by inverting thesample bottle, immersing it up to one meter below the water surface and slowly filling itas it is removed from the water. A Kemmerer sampler may also be used by holding it in ahorizontal position and closing it manually. Samples collected for chlorophyll analysisshould not be fixed or preserved. Chlorophyll samples should be preserved by chilling to4°C. If species composition analysis is necessary, then samples should be collected in aseparate sample bottle, or fixed or preserved by laboratory staff after the aliquot forchlorophyll analysis is removed from the sample container.When deeper samples are needed, use <strong>of</strong> a Kemmerer, water bottle, Van Dorn or Judaysamplers is standard. All <strong>of</strong> these sampling devices basically consist <strong>of</strong> a metal or plastichollow cylinder with remotely activated stoppers at both ends. The sampler is lowered toa desired depth with a graduated line. Once at the desired depth, a heavy brass slug or“messenger” attached to the line is released. It slides down the line, and strikes therelease mechanism on the sampler which pulls the stoppers tight against the open ends <strong>of</strong>the cylinder, trapping the sample <strong>of</strong> water inside. The sampler is then withdrawn and thewater emptied into the sample container via a small spigot or tube in one <strong>of</strong> the stoppers.Use only nonmetallic samplers when metal analysis, algal assays, or primary productivitymeasurements will be performed on the sample. Sample bottle labels should identify thebody <strong>of</strong> water sampled and list the date <strong>of</strong> collection, collectors name, preservative ifpresent, and the type <strong>of</strong> biological analysis desired (determination <strong>of</strong> dominant or bloomspecies, total cell count, etc.). It is important that labels clearly identify live planktonsamples as being unpreserved.<strong>Ecological</strong> <strong>Evaluation</strong> <strong>Technical</strong> <strong>Guidance</strong> Document 105Version 1.2 8/29/12
Appendix C - Surface Water Toxicity TestingFreshwater Test SpeciesThe most commonly used species for freshwater (salinity <strong>of</strong> 3.5 ppt or less) surface watertoxicity studies in <strong>New</strong> <strong>Jersey</strong> are the fathead minnow (Pimephales promelas) and thewater flea (Ceriodaphnia dubia). Rainbow trout (Oncorhynchus mykiss) and brook trout(Salvelinus fontinalis) are listed in the USEPA guidance, and brown trout (Salmo trutta)and bluegill (Lepomis macrochirus) are listed in the NJDEP guidance, but these fishspecies are not commonly used in <strong>New</strong> <strong>Jersey</strong>. Two other daphnid species (Daphniapulex and Daphnia magna) are also listed in both the USEPA and NJDEP guidance, butare not commonly used in <strong>New</strong> <strong>Jersey</strong>.Saltwater Test SpeciesThe most commonly used species for saltwater (salinity greater than 3.5 ppt) surfacewater toxicity studies in <strong>New</strong> <strong>Jersey</strong> are the sheepshead minnow (Cyprinodon variegatus)and the opossum shrimp (Americamysis bahia). Three other fish species ― inlandsilversides (Menidia beryllina), Atlantic silverside (M. menidia) and the tidewatersilverside (M. peninsulae) ― are also listed in both the USEPA and NJDEP guidance butare not commonly used in <strong>New</strong> <strong>Jersey</strong>. The USEPA guidance lists a sea urchin (Arbaciapunctulata) and a macroalga (Champia parvula), and the NJDEP guidance lists grassshrimp (Paleomonetes pugio), but these last three are rarely, if ever, used in <strong>New</strong> <strong>Jersey</strong>.Toxicity Test TypesThere are three basic types <strong>of</strong> aqueous toxicity tests:(1) static, nonrenewal tests in which the test solution is not changed throughout thetest. These tests have the advantages <strong>of</strong> being simple, with minimal physicaldisturbance <strong>of</strong> the test organisms, and the disadvantage that toxicants mayvolatilize or degrade during testing;(2) static-renewal tests in which the test organisms are exposed to fresh test solutionperiodically (e.g., every 24 hours). These have the advantage <strong>of</strong> being able toaddress the volatilization/degradation issue but are more labor-intensive and causemore physical disturbance to the test organisms; and(3) flow-through tests in which there is a continual or semi-continual flow <strong>of</strong> freshtest solution through the test chambers for the duration <strong>of</strong> the test. These testshave the advantage <strong>of</strong> exposing organisms in a more stream-like manner, butthese tests are significantly more labor-intensive and are also more expensive thanthe other two test types.Toxicity Test Duration - Acute or ChronicToxicity is generally assessed in the laboratory using acute or chronic studies. Acutestudies are <strong>of</strong> short duration, usually one to four days, and are designed to determinewhether the surface water sample in question will kill the exposed organisms. Chronicstudies are longer, usually seven days or more (some exceeding 90 days), and aredesigned to determine sublethal effects on growth and reproduction. While observedlethality is a direct indication that the sample in question is toxic, sublethal effects areimportant for the assessment <strong>of</strong> long-term population health and are generally theendpoint <strong>of</strong> concern in an ecological risk assessment (ERA).<strong>Ecological</strong> <strong>Evaluation</strong> <strong>Technical</strong> <strong>Guidance</strong> Document 106Version 1.2 8/29/12
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Acronyms and AbbreviationsADDAETAFA
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Executive SummaryThis document prov
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environmentally sensitive areas pur
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Sample SelectionAfter completing th
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higher trophic level receptors. Lip
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