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List of References List of references 1 ABBOTT, I.A., 1965. Helminthora and 16 ACHUTHANKUTTY, C.T. & S. AYYAPPAN NAIR, Helminthocladia from California. 25: 88-98. 1976. A new species of sergestid shrimp, Acetes orientalis 2 ABDEL KARIM, A.G., 1967. Algal Flora of Certain (Crustacea: Decapoda, Sergestidae) from Goa, Central Gravel Pits in the Thames Valley, U.K. 30: 577-599. West Coast of India. 48: 233-239. 3 ABDEL KARIM, A.G., 1975. Studies on the 17 ADAMS, T.G., G.J. ATCHISON & R.J. VETTER, Freshwater Algae of the Sudan. II.The distribution of 1980. The impact of an industrial contaminated lake on the Bacillariophyceae of Wadi Galol, Jebel Marra. 47: heavy metal levels in its effluent stream. 69: 187-193. 31-42. 18 ADEMA, D.M.M., 1978. Daphnia magna as a test 4 ABDEL KARIM,A.G. & O.M. SAEED, 1978. Studies animal in acute and chronic toxicity tests. 59: 125-134. on the freshwater algae of the Sudan. III. Vertical 19 ADEY, W.H., 1964. The Genus Phymatolithon in the distribution of Melosira granulata (EHREN.) RALFS. Gulf of Maine. 24: 377-420. in the White Nile, with reference to certain 20 ADEY, W.H., 1965. The Genus Clathromorphum environmental variables. 57: 73-79. (Corallinaceae) in the Gulf of Maine. 26: 539-573. 5 ABDEL MAGID, A.M. & M.M. BABIKER, 1975. 21 ADEY, W.H., 1966. The genus Pseudolithophyllum Oxygen Consumption and Respiratory Behaviour of (Corallinaceae) in the Gulf of Maine. 27: 479-497. Three Nile Fishes. 46: 359-367. 22 ADEY, W.H., 1966. The Genera Lithothamnium, 6 ABDEL-MALEK, S.A. & M.M. ISHAK, 1980. Some Leptophytum (nov. gen.) and Phymatolithon in the Gulf ecological aspects of Lake Qarun, Fayoum, Egypt. Part of Maine. 28: 321-370. II. Production of plankton and benthic organisms. 75: 23 ADHIKARY, S.P. & H. PATTNAIK, 1979. Growth 201-208. response of Westiellopsis prolifica JANET to organic 7 ABDELMALIK, W.E.Y., R.M.K. EL-SHINAWY, M.M. substrates in light and dark. 67: 241-247. ISHAK & K.A. MAHMOUD, 1973. Uptake of 24 AGARKAR, D.S., M.S. AGARKAR & R. DIKSHIT, Radionuclides by Some Aquatic Macrophytes of 1979. Desmids from Bandhavgarh, Madhya Pradesh, Ismailia Canal, Egypt. 42: 3-12. India. 65: 213-223. 8 ABDIN, G., 1949. Luminosity Measurements in 25 AGARKAR, M.S. & D.S. AGARKAR, 1977. Desmids Aswan Reservoir, Egypt. 1: 169-182. from Pachmarhi, Madhya Pradesh, India. 54: 23-32. 9 ABDIN, G., 1949. Biological productivity of 26 AGNEW, J.D., 1962. The Distribution of reservoirs. 1: 469-475. Centroptiloides bifasciata (E.-P.) (Ba~tidae: Ephem.) in 10 ABDIN, G., 1949. Benthic Algal Flora of Aswan Southern Africa, with Ecological Observations on the Reservoir (Egypt). 2:118-133. Nymphs. 20: 367-372. 11 ABEL RAHEEM, K., H. EL-GINDY & M.J. AL- 27 AGNEW, J.D., 1963. New South African Records of HASSAN, 1980. Interrelationship of molluscicidal Imperfectly Known Baetidae (Ephem.). 22: 41-46. concentration and temperature on the respiration of 28 AHMAD, M.R., 1966. Some Observations on the Bulinus truncatus. 74:11-15. Effect of Feeding Cirrhina mrigala (Ham.) with 12 ABU-GIDEIRI, Y.B., 1968. Observations on the Microcystis aeruginosa Kiitz. 28: 88-90. Behaviour of the Developing Zoarces viviparus 29 AHMAD, M.R., 1967. Algal Flora of Some Ponds of (Zoarcidae). 31: 60-64. Kanpur. 29: 156-164. 13 ABU-GIDEIRI, Y.B., 1969. The Development and 30 AHMAD, M.R., 1967. Observations on the Effect of Distribution of Plankton in the Northern Part of the Feeding Labeo rohita (HAM.) with Microcystis White Nile. 33: 369-378. aeruginosa K/itz. 29: 388-392. 14 ABU-GIDEIRI, Y.B. & M.T. ALI, 1975. A 31 AHMAD, M.R. & A. WINTER, 1970. The Effect of Preliminary Biological Survey of Lake Nubia. 46: 535- Weak Auxins on the Growth of Blue-Green Algae. 36: 541. 305-316. 15 ABU-GIDEIRI, Y.B. & D.H. NASR, 1973. Sound 32 AIKEN, R.B., 1979. A size selective underwater light Production by Synodontis schall (BLOCH- trap. 65: 65-68. SCHNEIDER). 43: 415-428. 33 ALEEM, A.A., 1957. Succession of Marine Fouling 53 ARMITAGE, K.B., 1971. A Highly Alkaline Lake in Organisms on Test Panels Immersed in Deep-water at Nicaragua. 38: 437-439. La Jolla, California. l 1: 40-58. 54 ARMITAGE, K.B. & M. DAVIS, 1967. Population 34 AL-KHOLY, A.A., M.M. ISHAK, Y.A. YOUSSEF & Structure of Some Pond Microcrustacea. 29: 205-225. S.R. KHALIL, 1970. Phosphorus Uptake from Water by 55 ARMITAGE, K.B. & B. SAXENA, 1973. Population Tilapia zilii (GERVAIS). 36: 471-478. Dynamics of Pond Zooplankton. I. Diaptomus pallidus 35 ALLANSON, B.R., 1958. On the Systematics of the HERRICK. 42: 295-333. Molluscan Genus Siphonaria in South Africa. 12: 149- 56 ARMITAGE, K.B., B. SAXENA & E.E. ANGINO, 180. 1973. Population Dynamics of Pond Zooplankton. II. 36 ALLANSON, B.R. & J.M.T.M. GIESKES, 1961. Daphnia ambigua SCOURFIELD. 42: 491-507. Investigations into the Ecology of Polluted Inland 57 ARMITAGE, K.B. & B.B. SMITH, 1968. Population Waters in the Transvaal. Part I. The Physical, Chemical Studies of Pond Zooplankton. 32" 384-416. and Biological Conditions in the Jukskei-Crocodile 58 ARM1TAGE, P.D., 1978. Downstream changes in System. Part II. An Introduction to the Limnology of the composition, numbers and biomass of bottom fauna Hartbeespoort Dam with Special Reference to the Effect in tees below cow green reservoir and in an unregulated of Industrial and Domestic Pollution. 18: 1-94. tributary Maize Beck, in the first five years after 37 ALLEN, H.L. & B.T. OCEVSKI, 1977. Limnological impoundment. 58: 145-156. studies in a large, deep, oligotrophic lake (Lake Ohrid, 59 ARMITAGE, P.D., 1978. Catches of invertebrate Yugoslavia). A summary of nutritional radiobioassay drift by pump and net. 60: 229-233. responses of the pelagial phytoplankton. 53: 49-54. 60 ARMITAGE, P.D., 1979. A folding artificial 38 ALLENBY, K.G., 1966. The manganese and calcium substratum sampler for use in standing water. 66: 245- content of some aquatic plants and the water in which 248. they grow. 27: 498-500. 61 ARMITAGE, P.D., 1980. The effects of mine 39 ALLENBY, K.G., 1967. The Manganese and drainage and organic enrichment of benthos in the river Calcium Contents of Some Aquatic Plants and the Nent system, Northern Pennines. 74:119-128. Water in Which They Grow. 29: 239-244. 62 ARORA, H.C., 1965. Studies on Indian Rotifera. 40 ALLENBY, K.G., 1968. Some Analyses of Aquatic Part VI. On a Collection of Rotifera from Nagpur, Plants and Waters. 32: 486-490. India, with four new Species and a New Variety. 26: 41 ALMAZAN, G. & C.E. BOYD, 1978. An evaluation 444-456. of Secchi disk visibility for estimating density in fish 63 ARORA, H.C., 1966. Rotifera as indicators of ponds. 61: 205-208. trophic nature of environments. 27: 146-159. 42 AL-SAADI, H.A., S.S. RATTAN, T.W. MUHSIN & 64 ARUMUGAM, P.T. & J.L FURTADO, 1980. Physico- H.A. HAMEED, 1979. Possible relation between chemistry, destratification and nutrient budget of a phytoplankton numbers and saprolegnioid fungi in lowland eutrophicated Malaysian reservoir and its Shatt AI-Arab near Basrah, Iraq. 63: 57-62. limnological implications. 70:11-24. 43 AMOROS, C., 1980. A simple device for 65 ARIJNACHALAM, S., E. VIVEI(ANANDAN& T.J. quantitative pseudoperiphyton sampling. 68: 243-246. PANDIAN, 1976. Food intake, conversion and swimming 44 AMSELLEM, J. & P. CLEMENT, 1980. A simplified activity in the air-breathing catfish Heteropneustes method for the preparation of rotifers for transmission fossilis. 51: 213-217. and scanning electron microscopy. 73:119-122. 66 ASIF, M., 1979. Hermaphroditism and sex reversal 45 ANANG, E.R., 1979. The seasonal cycle of the in the four common oviparous species of oysters from phytoplankton in the coastal waters of Ghana. 62: 33- the coast of Karachi. 66: 49-55. 45. 67 ASIF, M., 1980. The reproductive cycle in the 46 ANDERSON, J.G. & P.S. MEADOWS, 1969. Bacteria population of Saccostrea cuccullatta (Born) from the on Intertidal Sand Grains. 33: 33-46. coast of Karachi, Pakistan. 68: 73-79. 47 ANDERSON, K.B., E.F. BENFIELD & A.L. 68 ASMUND, B., 1955. Occurrence of Dinobryon BUIKEMA, Jr., 1977. Zooplankton of a swamp water crenulatum Wm. et G.S. West in some Danish ponds ecosystem. 55: 177-185. and remarks on its morphology, cyst formation, and 48 ANDERSON, R,S. & A.-M. de HENAU, 1980. An ecology. 7: 75-87. assessment of the meiobenthos from nine mountain 69 ASMUND, B., 1968. Studies on Chrysophyceae lakes in western Canada. 70: 257-264. from Some Ponds and Lakes in Alaska. VI. Occurrence 49 ANDERSSON, G., H. BERGGREN, G. CRONBERG & of Synura Species. 31: 497-515. C. GELIN, 1978. Effects of planktivorous and 70 ASMUND, B. & D.K. HILLIARD, 1961. Sudies on benthivorous fish on organisms and water chemistry in Chrysophyceae from Some Ponds and Lakes in Alaska. eutrophic lakes. 59: 9-15. I. Mallomonas Species Examined with Electron 50 ANSARI, Z.A., A.H. PARULEKAR & T.G. JAGTAP, Microscope. 17: 237-258. 1980. Distribution of sublittoral meiobenthos off Goa 71 ASMUND, B. & D.K. HILLIARD, 1965. Studies on coast, India. 74: 209-214. Chrysophyceae from Some Ponds and Lakes in Alaska. 51 ARAWOMO, G.A.O., 1980. The food of juvenile IV. Occurrence of Mallomonopsis Species in Brackish trout, Salmo trutta L., in Loch Leven, Kinross, Water. 26: 521-526. Scotland. 75: 49-56. 52 ARMITAGE, K.B., 1961. Distribution of Riffle Insects of the Firehole River, Wyoming. 17:152-174. 72 ASMUND, B.
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