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Dissolved Oxygen Study SHIPROCK HIGH San Juan River ENVIRONMENTAL SCIENCE Razor Back Sucker 2002-2008 I, II &AP LESSON MODULE Lesson Design: Ricky Espinoza ©2002 Grades 9-12 Essential Questions: • What is a Razor Back Sucker? Catostomus texanus • How does man affect this organisms population? • What is dissolved oxygen (DO)? • How can dissolved oxygen affect the health of a river? • What are the peripheral factors that affect the health of the Razor Back Sucker population? • Who or what are the players in this system? Environmentally, economically, and socially. •Can we create a mathematical model that will help us predict dissolved oxygen in the San Juan River? •How confident are we that our model is representing what is happening in nature? •What is the relationship between dissolved oxygen and temperature? •What would this relationship look like when graphed. •What applications of our model can you see being of use in our community. •What will be the impact of our data that is generated by our model and data collected on site (San Juan River)? The San Juan River is a resource for man as well a for Nature. What is a Razor Back Sucker? Catostomus texanus As the population in our area increases so will the demand for water. The main source of water in the San Juan River, is water stored and released from Navajo Dam. Before the dam was built our river had a self sustaining population of Razor Back Suckers. During the construction of the a program to poison fish was carried out in the early The poison used was Rotenone, the poison was poured into the three rivers which feed Navajo Lake to eradicate what were then considered trash fish (Razor Back Suckers) to allow the stocking of preferred game fish such as Rainbow trout and German browns. Now the Razor Back Suckers are an endangered species, protected by Federal laws. What is a Razor Back Sucker? Catostomus texanus Razorback sucker is a boney fish with the following characteristics: 1. Successfully reproduce in both lentic and lotic habitats (Minckley et al. 1991). 2. Fish mature between the ages of 4 and 7 when they reach between 400 and 450 mm. 3. Fish spawn on wind swept cobble and gravel shorelines 4. Fish can spawn near Dam tail waters however larvae that successfully hatch, but, survival in or near reservoirs is low because of larval predation from nonnative fishes and possibly low prey densities (Minckley et al. 1991). Trout will eat Razorback sucker larva. This is a rainbow trout from the San Juan River. 5. Spawning occurs between November and May when water temperatures are between 7 and 18°C with an average of about 15°C between mid-April to mid-May (Tyus and Karp 1990). 6. Razorback suckers spawn over gravel bars that are 0.1 to 1.0 meter deep with a water velocity between 0.1 and 0.6 meters per second (Wick et al. 1982). Razorback sucker can be a large fish in size and slightly compressed laterally. The upper body is dark brown to olive green and pale white or lemon yellow on the lower abdominal surfaces. The razorback sucker was originally described as Catostomus texanus from a specimen collected from Arizona (Abbott 1861). 7. The duration of spawning varies with flow patterns, but generally lasts between four and six weeks (Tyus and Karp 1990, Modde and Wick, 1995). Although natural spawning occurs annually and larvae have been collected from the main spawning sites, few juvenile fish have ever been collected in the wild since mid-1960's (Minckley et al. 1991). Remember that they poisoned with Rotenone, the poison was poured into the three rivers which feed Navajo Lake to eradicate what were then considered trash fish (Razor Back Suckers) to allow the stocking of preferred game fish such as Rainbow trout and German browns. Could this be the reason we don’t see them in the wild? The greatest threats to the razorback sucker include: • Alteration of natural flows regimes • Interactions with nonnative predators (Minckley 1991). • Reservoirs have created barriers to spawning and migrations. • Dams alter the natural seasonal river cycles, thus removing cues associated with migrations. (Stephens et al. 1992). • Selenium concentrations that are capable of impairing reproductive success. • Storage of the water from major tributaries have transformed warm rivers with variable flows into clear, cold/cool water environments that, in some areas, are more suitable environments for nonnative fish like salmon and trout. Fishes native to the system like the razorback sucker have extreme difficulty in these conditions. • Because reservoir environments discharges controlled by reservoir releases are not characterized by the variation in flows, sedimentation, temperature, dissolved oxygen, etc. characteristic of the historic environment, nonnative warm water fishes have become more effective competitors and predators on native species, including the razorback sucker (Minckley et al. 1991). • Localized contaminant buildup threats exist in stored waters. • The razorback sucker's diet consists of vegetable matter and material from river bottom ooze • • Conservation Action In 1988 an interagency effort formed the Recovery Implementation Program for the Recovery of Endangered Fishes in the Upper and Lower Colorado River to fund and administer recovery efforts for the razorback sucker. Programs the 1988 program is made up of a consortium among the U.S. Fish and Wildlife Service, U.S. Bureau of Reclamation and other interest. This program outlines a 15 year effort consisting of five elements: 1. Provision of in-stream flows 2. Habitat development and maintenance 3. Native fish stocking 4. Management of nonnative species and sport fishing 5. Research, monitoring and data management. The goal of this program is to maintain and protect self- sustaining populations of the Razor Back Sucker and sufficient natural habitat to sustain these populations. This program should be beneficial to other endangered fish species sharing this habitat, including bonytailed chub, Colorado squawfish, and humpback chub This species was listed as an endangered species by the U.S. Fish and Wildlife Service in 1991 (U.S. Fish and Wildlife Service 1991). Experimental releases in the Upper Basin, and attempts to propagate Razor Back Suckers in Lower Basin reservoirs are encouraging, but the mainstream Colorado River populations continue to decline. Upper and Lower Colorado River as well as major tributaries that feed the Colorado River are part of this program. The San Juan River is one of these rivers. Shiprock High School is performing a six year study that will examine dissolved oxygen and its relationship with temperature due to flow rate changes. An interim progress report for razorback sucker monitoring trips conducted in 2003 will be completed by 31 March 2004. Now at this time we as a class, can get that report and input this data into our models, that we will build, to see how real data compares to calculated numbers. Our models will be built on Microsoft Excel. When we graph the data side by side we will start to see patterns that can help us explain the patterns we see in nature. That is real science at work. The biggest problem associated with achieving higher numbers of San Juan River razorback suckers is RBS larvae production: • Rearing facilities outside of the San Juan River Basin lack the capabilities to hold and rear razorback sucker for the San Juan River Recovery Implementation Program (SJRIP). • SJRIP undertook efforts to obtain or build grow-out ponds within the San Juan River basin that would afford a measure of self-sufficiency (for holding/rearing fish) to the San Juan River razorback sucker augmentation program. Beginning in 1997, a series of grow-out ponds were established on NAPI lands southwest of Farmington, New Mexico. Presently there are about 16 surface acres of grow-out ponds (i.e., nine individual ponds) being used to rear razorback sucker. An additional nine acres of grow-out ponds are scheduled to be built in fall/winter 2002-2003. The changes is river temperatures also in turn will change the dissolved oxygen properties of the river. • The UNM holding facility serves to maintain larvae in the interim between the time for release and grow out. (8-10 weeks) between their being obtained from hatchery facilities and a time when water temperatures at grow-out ponds increases to a sufficient level for rearing. These larvae will then be stocked in three of the nine available grow-out ponds and eventually released into the wild. The decline of Razor Back Sucker has been attributed to thermal regime changes. Water quality parameters including dissolved oxygen, water temperature, conductivity, flow rates and pH will be measured at each contact location. Larval Razor Back Suckers drift downstream from the spawning habitat, and concentrate in warm, low-velocity areas (e.g., flooded bottoms). These areas also support post-larval RBS, and channel and mid-stream river habitats floored by fine-grained alluvium are important to subsequent RBS life stages (Minckley 1983, Tyus and Karp 1989, Minckley 1991). Some Razor Back sucker may be implanted with radio transmitters (one-year lifespan) on 2002 sampling trips. These fish will be tracked throughout the suspected spawning season for razorback sucker in the San Juan River this may give us an insight into their migration patterns. Electro fishing and handling of rare fish species will follow the protocol found in the main channel fish community monitoring work plan, except that only data on rare fish species collected (i.e., razorback sucker, Colorado pikeminnow, and roundtail chub) will be recorded. When rare fish species are collected, PIT tag number, length, weight, reproductive status (if evident), and information about health abnormalities (if any) will be recorded. Survival rates are determined using either mark and recapture models. Intensive efforts to maintain the last large population of razorback sucker in Lake Mohave include techniques depicted in previous photos and photos to come. (1994-1997) approximately, 6,836 razorback sucker have been stocked into the San Juan River. This represents a short fall of about 76,600 razorback suckers when compared to numbers recommended in the five-year recommended numbers to be stocked. Because of the large shortfall in numbers of stocked fish during the 1997-2001 augmentation effort, the San Juan River Biology Committee adopted an addendum to the 1997 stocking plan that extends the intensive stocking period for razorback sucker for an additional eight-year period, beginning in 2004 and continuing through 2011. This addendum calls for stocking a minimum of 11,374 razorback sucker per year, with the goal of establishing an adult population of 5,800 adult razorback sucker in the San Juan River. Springtime concentrations of adult Razor Back Suckers have been noted in side-channels, off-channel impoundments, and in tributaries (Bestgen 1990, Minckley 1991), in temperatures of 22 to 25oC (Bulkley and Pimentel 1983); however, RBS occur in widely varying temperatures. RBS habitats in the Upper Colorado River Basin are ice-covered during winter, while the temperatures of mainstream habitats in the Lower Colorado River exceed 90oF (Dill 1944). Click trout to view lab. Click trout to view Excel DO model Click trout to view DO Model Click trout to view Evaluation Tool Click trout to view Lesson Plan Calculation notes Data Sheets & Graphs References and acknowledgements: 1. Abbott, C.C. 1861. Descriptions of four new species of North American Cyprinidae. Proceedings of the Philadelphia Academy of Natural Sciences 12(1860):473-474. 2. Bestgen, K.R. 1990. Status review of the razorback sucker, Xyrauchen texanus. Larval Fish Laboratory Contribution 44, Colorado State University, Fort Collins, Colorado. 3. Bozek, M.A., L.J. Paulson, and G.R. Wilde. 1990. Effects of ambient Lake Mohave temperatures on development, oxygen consumption, and hatching success of the razorback sucker. Environmental Biology of Fishes 27:255-263. 4. Gutermuth, F.B., L.D. Lentsch, and K.R. Bestgen. 1995. collection of age-0 razorback suckers (Xyrauchen texanus) in the lower Green River, Utah. The Southwestern Naturalist 39:389-391. 5. Hubbs, C.L. and Miller, R.R. 1953. Hybridization in nature between the fish genera Catostomus and Xyrauchen. Papers of the Michigan Academy of Science, Arts, & Letters 38, 207-233. 6. Kirsch, P.H. 1889. Notes on a collection of fishes obtained in the Gila River at Fort Thomas, Arizona. Proceedings of the U.S. National Museum 11:555-558. 7. Lanigan, S.H., and H.M. Tyus. 1989. Population size and status of the razorback sucker in the Green River basin, Utah and Colorado. North American Journal of Fisheries Management 9:68- 73. 8. Lanigan, S.H., and H.M. Tyus. 1989. Population size and status of the razorback sucker in the Green River basin, Utah and Colorado. North American Journal of Fisheries Management 9:68- 73. 9. McAda, C.W., B. Bates, S. Cranney, T. Chart, B. Elmblad, and T. Nesler. 1994. Interagency standardized monitoring program: Summary of results, 1986 though 1992. Final Report. Recovery Program for the Endangered Fishes of the Upper Colorado River Basin. U.S. Fish and Wildlife Service, Denver, CO. 10. McCarthy, M.S., and W.L. Minckley. 1987. Age estimation for razorback sucker (Pisces: Catostomidae) from Lake Mohave, Arizona-Nevada. Journal of the Arizona-Nevada Academy of Sciences 21:87-97. 11. Marsh, P.C. 1987. Food of adult razorback sucker in Lake Mohave, ArizonaNevada. Transactions of the American Fisheries Society 116:117-119. 12. Marsh, P.C. and D.R. Langhorst. 1988. Feeding and fate of wild larval razorback suckers. Environmental Biology of Fishes 21:59-67. 13. Marsh, P.C. 1993. Abundance, movements, and status of adult razorback sucker, Xyrauchen texanus, in Lake Mohave, Arizona and Nevada. Proceedings of the Desert Fishes Council, Volume 25: 35-36 (Abstract). 14. Minckley, W.L. 1973. Fishes of Arizona. Arizona Game and Fish Department, Phoenix. 293 pp. 15. Minckley. W.L. 1983. Status of the razorback sucker, Xyrauchen texanus (Abbott), in the lower Colorado River basin. The Southwestern Naturalist 28:165-187. 16. Minckley, W.L., P.C. Marsh, J.E. Brooks, J.E. Johnson, and B.L. Jensen. 1991. Management toward recovery of the razorback sucker. Pages 283-357, in W.L. Minckley and J.E. Deacon eds., Battle against extinction: Native fish management in the American West. University of Arizona Press, Tucson, AZ. 17. Modde, T., A.T. Scholz, J.H. Williamson, G.B. Haines, B.D. Burdick, and F.K. Pfeifer. 1995. Augmentation plan for razorback sucker in the Upper Colorado River Basin. American Fisheries Society Symposium 15:102-111 19. Modde, T., K.P. Burnham, and E.F.Wick. 1996. Population status of the razorback sucker in the middle Green River. Conservation Biology 10:in press. 20. Modde, T., E.J. Wick. 1995. Spring habitat use and availability to razorback sucker in the middle Green River. Draft Final Report. Recovery Program for the Endangered Fishes of the Upper Colorado River Basin. U.S. Fish and Wildlife Service, Denver, CO. 21. Papoulias, D. and W.L. Minckley. 1990. Food limited survival of larval razorback sucker, Xyrauchen texanus, in the laboratory. Environmental Biology of Fishes 2 9:73-78. 22. Stephens, D.W., B. Waddell, L.A. Peltz, and Jerry B. Miller. 1992. Detailed study of selenium and selected elements in water, bottom sediment, and biota associated with irrigation drainage in the middle Green River Basin, Utah, 1988-1990. U.S. Geological Survey, Water-Resources Investigations Report 92-4084. U.S. Geological Survey, Salt Lake City, Utah 23. Taba, S.S., J.R. Murphy, and H.H. Frost. 1965. Notes on the fishes of the Colorado River near Moab, Utah. Proceedings of the Utah Academy of Sciences, Arts, and Letters 42:280-283. 24. Tyus, H.M. 1987. Distribution, reproduction, and habitat use of the razorback sucker in the Green River, Utah, 1979-1986. Transactions of the American Fisheries Society 116:111-116. 25. Tyus, H.M., and C.A. Karp. 1990. Spawning and movements of razorback sucker, Xyrauchen texanus, in the Green River basin of Colorado and Utah. Southwestern Naturalist 35:427-433. Vanicek, C.D. 1967. Ecological studies of native Green River fishes below Flaming Gorge Dam, 1964-66. Ph.D. Dissertation, Utah State University, Logan. 26. U.S. Fish and Wildlife Service (USFWS). 1991. Endangered and threatened wildlife and plants: the razorback sucker,(Xyrauchen texanus). Determined to be an endangered species. Federal Register 56(205):54957-54967. Waddell, B., and T. May. 1995. Selenium concentrations in the razorback sucker (Xyrauchen texanus): substitution on non- lethal muscle plugs for muscle tissue contaminant assessment. Archives of Environmental Contamination and Toxicology 28:321- 326. 27. Wick, E.J., C.W. McAda, and R.V. Bulkley. 1982. Life history and prospects for recovery of the razorback sucker. Pages 120-126 in W.H. Miller, H.M. Tyus, and C.A. Carlson (eds.), Fishes of the Upper Colorado River system: present and future. Western Division, American Fisheries Society, Bethesda, Maryland. 28. Wydoski, R.S., and J. Hamill. 1991. Evolution of a cooperative recovery program for endangered fishes in the Upper Colorado River Basin. Pages 123-135, in W.L. Minckley and J.E. Deacon eds., Battle against extinction: Native fish management in the American West. University of Arizona Press, Tucson, AZ. 29. Compiled by Tim Modde and Dick Wydoski U.S. Fish and Wildlife Service Colorado River Fish Project 266 W. 100 N., Suite 2 Vernal, UT 84078 [email protected] December 10, 1995. 30. LaRivers, Ira. 1994. Fishes and fisheries of Nevada. University of Nevada Press, Reno, Nevada. 31. Johnson, James et. al. 1993. Transactions of the American fisheries society. American Fisheries Society, Lawrence, Kansas. 32. http://www2.vernier.com/sample_labs/computer/water_quality/dissolved_oxygen.pdf 33. http://aquanic.org/images/tools/oxygen.htm