CALIFORNIA FISH™GAME "CONSERVATION OF WILDLIFE THROUGH EDUCATION" California Fish and Game is a journal devoted to the conservation of wild- life. Its contents are not copyrighted and may be produced elsewhere provided credit is given the authors and the California Department of Fish and Game. Interested persons may have their names placed on the mailing list by writ- ing to the editor. There is no charge, but subscriptions must be renewed annu- ally by returning the postcard enclosed with each October issue. Subscribers are asked to report changes in address without delay. Please direct correspondence to: Mr. Phil M. Roedel, Editor California State Fisheries Laboratory Terminal Island Station San Pedro, California u 0 VOLUME 39 APRIL, 1953 NUMBER 2 Published Quarterly by ihe CALIFORNIA DEPARTMENT OF FISH AND GAME SACRAMENTO STATE OF CALIFORNIA DEPARTMENT OF FISH AND GAME EARL WARREN Governor FISH AND GAME COMMISSION WILLIAM J. SILVA, President Modesto LEE F. PAYNE, Commissioner CARL F. WENTE, Commissioner Los Angeles San Francisco HARLEY E. KNOX, Commissioner WELDON L. OXLEY, Commissioner San Diego Redding SETH GORDON Director of Fish and Game CALIFORNIA FISH AND GAME PHIL M. ROEDEL, Editor Terminal Island Editorial Board RICHARD S. CROKER Sacramento FRANK KOZLIK Sacramento LEO SHAPOVALOV Sacramento TABLE OF CONTENTS Nutritive Value for Deer of Some Forage Plants in the Sierra Nevada I • erbert L. I [agen 163 studies of Black-tailed Deer Reproduction on Three Chaparral Cover Types Richard D. Taber 177 A Possible Method of Increasing Western Mountain Mahogany on Game Ranges II. II. Biswell, A. M. Schultz and I). W. Hedrick 181 Progress Reporl on a Study of the Kelp Bass, Paralabrax chilli nil us Robert I). Oollyer and Parke II. Yur.\<; 191 Aquarium Tests of Tags on Striped Pass A.J.Calhoun 209 The Effed of the Commercial Canning Process I'pon Puffer Poison Bruce W. Halstead and Norman C. Pinker 'JP» A Preliminary Report on the Toxicity of the Gulf Puffer. Sphoe- roides annulatus ..Don R. Goe and Bruce W. Balstead 229 Observations on the Effect of Black Powder Explosions on Pish Life Donald IT. Fry, Jr.. and Keith W. Cox 233 The 1952 Shark Derbies at Elkhorn Slough, Monterey Bay. and at Coyote Point, San Francisco Bay ... _Earl S. Herald 237 New Fishways on the Yuba and Feather Rivers _. ._ J. A. Aim. in 245 Official Common Names of Certain Marine Fishes of California Phil M. Roedel 253 Notes New Records of Pacific Sardine and Pacific Mackerel in the Gulf of California Boyd AY. Walker 263 Survival of Some Fishes Recently Introduced into the Salton Sea. California P. A. Douglas 264 The Bramble Shark (Echinorhinus brucus) at Guadalupe Island, Mexico Robert D. Collyer 266 Reviews 267 Reports ___. 271 ( Kit ) NUTRITIVE VALUE FOR DEER OF SOME FORAGE PLANTS IN THE SIERRA NEVADA' By HERBERT L. HAGEN Bureau of Game Conservation, California Department of Fish and Game INTRODUCTION Various investigations into the problems of managing North American deer have demonstrated thai local populations oft en arc limited by in- adequate supplies of nutritions forage. With the control of large preda- tors and the enactment and enforcement of stringent protective laws. many deer herds have increased to the point where they have outst ripped their food supplies and large numbers have perished, either from mal- nutrition or by disease whieb becomes epizootic in undernourished popu- lations. It is now almost a maxim among game managers in the United States that die-offs among deer are a manifestation of inadequate nutri- tion. Food habits studies of deer on many ranges have shown that the ani- mals actually consume small quantities of a great variety of plants, but in each area they seem to be largely dependent for their sustenance during the critical season of the year, ordinarily the winter, on a few species which commonly are referred to as Key Forage Species. Symp- toms of distress (lowered fawn production, disease, or malnutrition) usually become evident in local populations when the key species are over-browsed even though second choice foods which normally are lightly utilized may still be abundant. Practically all deer that die of malnutri- tion do so with full stomachs — but full of foods which will not sustain them. Thus the problem of adequate nutrition for deer is qualitative as well as quantitative, and it is important that we have a better under- standing of the chemical composition and actual nutritive value of forage plants in order to understand the limitations imposed by range on deer populations. PREVIOUS INVESTIGATIONS Previous investigators faced with this problem have used two prin- cipal approaches in studying deer nutrition: (1) chemical analysis of 1 Submitted for publication October, 1952. Most of the material presented here was sub- mitted to the University of California, Museum of Vertebrate Zoology, in partial ful- fillment of requirements for the master of arts degree in 1949. The writer expresses appreciation to Dr. Harold H. Goss of the University of California College of Agriculture at Davis, whose guidance and help aided greatly in this study ; to Dr. A. Starker Leopold of the Museum of Vertebrate Zoology under whose direction this study was made, and to the members of the California Department of Pish and Game disease and food habits laboratory, without whose cooperation this study would have been impossible. (163) 164 CALIFORNIA FISH AXD GAME forage samples and (2) actual feeding experiments with penned deer. Some have used both in combination, as was done in this study. Feeding Experiments Xiehol (1938) in Arizona fed captive deer to determine quantities of feed needed for maintenance. He found they required 2.2 pounds of hay and grain or 2.3 pounds of native feeds daily per 100 pounds live weight to maintain themselves in good condition. Other studies designed to test qualitative differences in feeds have been reported by Maynard, et al. (1935), Atwood (1948), and Davenport (1939). All found that some forage species are more nutritious than others, but that, in general, deer do better on mixtures of foods than any single species. Maynard et al. (1935) and Forbes et al. (1941) ran digestion trials to determine the digestive capacities of deer, in comparison with goats and rabbits re- spectively. It was found that goats were better able to digest roughages (crude fiber) than deer, and that deer were more efficient than rabbits. Chemical Analysis of Forage Plants Hellmers (1940) in Pennsylvania made a study of the monthly varia- tion in the chemical composition of deer foods and found that the nutri- tive values decreased during the winter. Gordon and Sampson (1939) also found a decrease in nutritive value of foothill range plants in Cali- fornia from summer through fall and winter. Aldous (1945) in Nevada found by analysis of clippings of bitterbrush that the twig tips were more nutritious than basal sections. Reynolds and Sampson (1943) in California found that the sprouts of burned-over chamise were more nutritious than those from unburned plants. Likewise Binarsen (1946) in Oregon showed that the protein content of forage plants from burned areas was higher than from unburned areas, and correspondingly that the burned-over areas had a higher population of heavier and healthier deer. Swift (1948) in Pennsylvania observed that in grain and hay fields the deer singled out certain areas where the plants proved to be higher in fat. calcium and phosphorus. In summary, it seems that deer eat a wide variety of foods, but that some of the foods are more important in sustaining the animals than others. There seems to be considerable variation in quality between for- age species, and likewise there are seasonal changes within a species dur- ing different growth stages. Sprouts are more nutritious than old growth and a given twig will lose nutritive value through the dormant winter season. The tip of a twig, which normally is the portion consumed first, is richer than the basal section. In general, the best foods (most palatable and most nutritious) are high in crude protein and sometimes also in minerals and fats. FORAGE STUDIES ON THE JAWBONE WINTER RANGE In 1947 the University of California undertook an intensive investiga- 1 ion of a herd of deer that winter on Jawbone Ridge in central Tuolumne ( lounty oil the western slope of the Sierra Nevada. This study was made in cooperation with the California Department of Fish and Game with NUTRITIVE VALUE OF FOB USE PLANTS 165 Pittman-Robertson funds and included range and food habits investiga- tions, and a study of general health and productivity in the herd. A re port on the Jawbone study has now been published, Leopold ei al. I 1 951 I Work on nutritive value oi" browse species was centered here because of the background material available. The Jawbone winter range occupies about 24,000 acres on the lower part of Jawbone Ridge, which lies between the Tuolumne River on the south and the Clavey River on the north and west. Vegetation types on this area are listed in Table L. Of the five types, the "mixed brush," oc- cupying a little over a quarter of the area, furnishes I he bulk of the good deer forage. TABLE 1 Areas Occupied by Various Classes of Vegetation on the Jawbone Winter Range Vegetation type Acres Percent Coniferous timber 10,832 6,650 1,275 373 15.5 28.0 19.6 5.3 1.6 Totals -.- - 23,791 100.0 From the standpoint of deer nutrition the more important brushy species of plants on the winter range are : (1) buck brush, (2) mountain misery, (3) manzanita, (4) oaks, and in addition, grass in the spring. TABLE 2 Stomach Contents of 24 Deer Collected on the Jawbone Winter Range in 1948-49 (From Ferrel and Leach, 1950) Forage plant Mountain misery (Chamaebatia foliolosa) Buck brush (Ceanothus cuneatus) Manzanita (Arctostaphylos spp.) Grass (Graminae) Oaks unidentified (Quercus spp.) Maul Oak (Quercus chrysolepis) Christmas berry (Photinia arbuti folia) _ _ Stone crop (Sedum spathuli folium) California Black Oak (Quercus kelloggii) Incense cedar (Libocedrus decurrens) Willow (Salix spp.) Miscellaneous food items Forbs unidentified Browse unidentified Percent Percent volume occurrence 37.3 75 12.2 63 11.2 67 9.1 92 6.7 42 4.6 13 4.0 21 3.1 4 3.0 29 3.0 38 1.9 8 1.4 88 1.3 58 1.2 38 166 CALIFORNIA FISH AND GAME Table 2 presents the results of a food habits study made by Ferrel and Leach (1950), based on stomach samples of 24 deer taken from the Jaw- bone winter range. Range measurements and field observations show that l>iu-k brush is clearly the key forage species, and that mountain misery is taken in quantity only late in the winter when the buck brush becomes heavily browsed. The diet appears to be influenced by preference and is only secondarily a function of abundance. This would be much more striking if it were possible to illustrate the heavily browsed condition of the buck brush and the light use of the more abundant manzanita and mountain misery. In comparing the nutritive value of some of the foods eaten by Jawbone deer, the basic methods of previous investigators were used, i.e., (1) chemical analyses of twig and leaf samples to determine percent of fats, carbohydrates, protein, crude fiber and mineral matter, and (2) actual ili-estion trials. The digestion trials covered only one species (buck brush) to determine the digestibility of the plant, as well as the digestive coefficients of the fat, carbohydrates, protein, crude fiber and mineral matter. Chemical Analyses of Deer Foods For the chemical analyses, samples of buck brush (Ceanothus cune- atus), mountain misery (Chamebatia foliolosa), deer brush (Ceanothus integerrimus), hardtack (Cercocarpus betuloides), and two species of manzanita (Arctostaphylos patula and A. mariposa) , were collected at various times during two winters from the Jawbone winter range. Sam- ples of two species, snow brush (Ceanothus corclulatus) , and bitter cherry (Prunus emarginata), were collected from the Jawbone summer range. Samples of six species were collected from the summer range of the Tehama deer herd, in the area between the north side of Lake Almanor, Plumas County, and Lassen National Park. These were snow brush, squaw carpet (Ceanothus prostratus), tobacco bush (Ceanothus velu- tinus), serviceberry (Amelanchier alnifolia), mazanita (A. patula) and bitterbrush (Purshia tridentata) . Samples, unless otherwise noted, consisted of the terminal two inches of twigs and leaves of the plants. All were collected at random from a number of different plants in the same general area with the idea of approximating the amount of forage removed by the deer. The analyses were made at the California Department of Fish and Game Laboratory in Strawberry Canyon, Berkeley. The Association of Official Agricultural Chemists methods of analysis were used throughout. Jawbone Range Samples Buck brush (Ceanothus cuneatus) — Seven samples of buck brush were collected, one in October, one in December, one in February and four in April. Results of the analyses are given in Table 3. \l TI.TI i\ i; \ AM E OF FOR \ne Eawn (No. 1) was obtained from Tehama County, California, and the other (No. 2) came from Contra Costa County, California. Both wen- Colum- bian black-tailed deer (Odocoileus hemionus colnmbianus ) . Two pens 16 feet by 8 feet were built with well-drained cement floors and 8-foot hogwire sides. Feed troughs were installed, the design being a modification of the feeding troughs used by Nichols (1938). The forage used in the digestion trial was buck brush (Ceanothus cuneatus) obtained from between Sonora and Columbia in Tuolumne County. This forage was taken from an area where there was a large quantity of unbrowsed brush available, rather than from Jawbone Ridge where the deer had browsed the brush down to the point where it would be extremely difficult to collect the amount needed to run the digestion trial. During the winter of 1948-49, 67 percent of the 1948 growth was removed from the buck brush by the deer on Jawbone Ridge. An attempt was made to remove approximately the same percentage of the plant for use in the digestion trials. The forage was taken to the University of California College of Agri- culture at Davis, California, and dried in a hot air oven at a temperature of 50-55 degrees centigrade for five days. It was then ground in a ham- mer mill until it would pass through a one-eighth-inch mesh screen. It was exposed to the air long enough for the moisture in the feed to come to an equilibrium with the moisture in the air. In March, 1949, the two deer were nine months old and had been on hard feed for several months when the digestion trial was started. The feed was placed in pans, and the feed and pan weighed. The feed was left in front of the deer for 24 hours and then removed and the pan and remaining feed weighed. The difference was considered to be the amount of feed the deer had consumed in the 24-hour period. Apparently the feed in this dried and ground condition was not very palatable to the deer. According to Nichol's (1938) findings that a deer needs about 2.3 pounds of forage per day for each 100 pounds of live weight, these two deer did not eat enough of the forage to maintain them- selves. Where they should have consumed about 1.2 pounds apiece per day they only ate from one-third to three-fourths of a pound per day. The consumption varied from day to day wTith the individual deer. The feces were all collected and dried and stored in a jar until the trial was over ; then they were carefully dried to drive off all moisture and weighed. The deer were weighed and a blood sample taken at the start of the digestion trial. A red blood count was made from the blood samples and in comparison with counts found in wild deer showed the two deer to be in excellent condition at the start of the trial. The two deer were placed on the buck brush diet four days before the trial was started. However, deer No. 2 would not eat enough of the feed to start a trial until the eighth day had passed. There was an eight-day trial on deer No. 2 and a 12-day trial on deer No. 1. The two deer were on the buck brush for 16 days. During this period they lost some weight. 172 CALIFORNIA FISH AND GAME TABLE 5 Weight Losses of Experimental Animals During the Digestion Trial Deer No. Weight at start of trial, lbs. Weight at end of trial, lbs. Loss in weight, lbs. Percent of weight lost 1 ... 57^ 65 51 56 6V2 9 11.3 2 13.8 Table 5 shows the weights at the start of the trial and the end of the trial and the loss of weight of each deer. This loss in weight was probably not the result of the quality of the feed, but rather that the deer would not eat enough of it in the ground form to maintain their weight. In eight days deer No. 2 consumed 1,699.1 grams of buck brush for an average consumption of 212.4 grams per day. During this time he voided 897.0 grams of feces for an average of 112.1 grams per day, and a total digestibility of 47.2 percent. Deer No. 1 in 12 days consumed 3,363.3 grams of buck brush for an average consumption of 280.3 grams per day. During this time he voided 1,695.5 grams of feces, an average of 141.0 grams per day and total digestibility of 49.7 percent. TABLE 6 Digestive Coefficients of Buck Brush (Ceanothus cuneatus) Deer No. 1 Deer No. 2 Average for both Alfalfa hay T.D.N. 49.70 47.20 48.45 50.30 Protein 23.5 24.2 23.8 72.0 Fat 47.7 50.8 49.2 32.0 Min. matter 33.9 45.8 39.8 Crude fiber 36.4 32.9 34.6 43.0 N.F.E. 61.5 58.1 59.8 71.0 Tin- digestive coefficients of the deer for the buck brush and average digestive coefficients of alfalfa hay as given by Morrison (1949) are shown in Table 6. The comparison of the chemical analyses of alfalfa and buck brush are given in Table 4. The important difference in these two feeds appears to be in the protein, a feed high in protein is generally considered to be the more valuable. In the digestion trial it will be noted that there were some differences in the digestive capacities of the two deer. It is interesting that deer Xo. ] from Tehama County had a better digestibility of the crude fiber and the nitrogen free extract, and a better total digestibility of the buck brush. Although neither of the deer had ever seen buck brush before, the deer from Tehama I lounty, where buck brush is one of the most important deer foods, was better able to assimilate it and started eating large quan- tities of it much sooner than the deer from Contra Costa County, where buck brush is relatively rare and not an important deer food. The analysis indicates that buck brush has nearly as great a percentage of total digestible nutrients as has alfalfa hay. Evidently buck brush and probably some of the other wild forage plants are better foods, at least for deer, than has heretofore been realized. The most striking thing M fTRITIVE VALUE OP I '( >H J.GE PLANTS 17:; aboul the digestion trial was the low digestibility of the protein in the buck brush. It proved to I ly aboul ■ third as digestible as the pro tein in the alfalfa. It is unusual to find protein so low in digestibility in a feed Like buck brush thai is so high in total digestibility. It would seem thai the protein found in the Feed Late in the winter, when the protein content is probably the lowest of any time during the year, is of a very poor qua lit \ . Morrison (1949) states that when a ration contains too little protein in proportion to the amounts of easily digested carbohydrates the digesti bility of the ration may be seriously reduced. He also states thai in feeds low iii protein the digestibility of the protein itself may be reduced. In discussing maintenance requirements of farm animals. Morrison says that animals on a ration below the maintenance level of required protein will gradually lose weight because of the continuous small waste of protein from the tissues of the body. Such undernourished animals cannot long survive. Guilbert (1042) states that animals on a protein intake below the required maintenance level may have reproductive failures. Prom Einarsen's (1946) study on protein in the feeds utilized by deer in Oregon, it appears that protein is an important factor in deer nutrition. Thus it would seem that the protein may be the most important component of the feed, and the most important factor in the maintenance of the deer in good condition during the winter. At the time the deer were weighed at the end of the trial another blood sample was taken. Table 7 shows the results of the blood counts and the changes in hemoglobin. TABLE 7 Results of Blood Studies During the Digestion Trial Start of trial End of trial Deer No. 1 — Red blood cells in millions 14.1 112 14.3 111 9.4 80 Deer No. 2 — Red blood cells in millions _ 13.5 Percent hemoglobin 80 The difference between the two animals in red blood cell count did not correspond with the appearance of the deer. Deer No. 2 appeared to be in much poorer condition at the end of the trial and it lost more weight. However, a few days after the trial ended, deer No. 1 died of hemorrhagic septicemia. The organism was one of the Pasturella group causing fowl cholera. Diagnosis was made by the California Department of Fish and Game disease laboratory. Generally, healthy animals are not considered to be susceptible to this organism. Evidently the poor condi- tion and low vitality of deer No. 1, which was reflected much more ac- curately in the red blood cell count than in its appearance, was respon- sible for the deer being susceptible. SUMMARY Chemical analysis of samples of deer forage plants show marked dif- ferences in composition of the various species. There are also ureal differences between the chemical composition of the forage plants utilized 174 CALIFORNIA FISH AND GAME by the deer during the summer, and those plants utilized by the deer during the winter. The most significant contrast between "good" and "poor" forage species seem to be in crude protein content. Plants preferred by the deer and generally considered the best forage on the basis of range evaluation prove to be consistently high in protein, while the "emergency" or "stuffing" feeds are low in protein. Differences in fat and mineral content exist and may have a bearing on palatability and general nutritive value, but seem to be less important than protein content. Besides the differences between species it was found that protein content varies seasonally within a given species, being high in the summer and low in late winter. Average loss of protein content, October to April, proved to be about 25 percent in three species (hardtack, mountain misery and buck brush), represented by seasonal samples. The loss was most noticeable in hardtack and least noticeable in buck brush. The plants on the summer range have the highest protein content in the spring and decline during the summer. Deer have forage of high quality available immediately upon reaching the summer range. This may have some effect on fawn production, and probably has a beneficial effect on lactation. On an overstocked winter range such as Jawbone Ridge, the average nutritive value of the food consumed by an individual deer decreases through the winter because (1) the better terminal twig ends are con- sumed first, and (2) the protein, fat and mineral content of all species is decreasing throughout the winter. The low ebb in nutrition is reached in late winter, a time when most losses in deer herds occur. Actual digestion by deer of buck brush proved (experimentally) to be as efficient as digestion of good hay by cattle, except that the assimilation of protein by the deer was low. Broad conclusions are not justified on the basis of this limited test. However, it is possible that inefficient or low protein digestion may further augment the protein deficiency or- dinarily encountered by the deer in their late winter diet. REFERENCES Aldous, C. M. 1045. A winter studv of mule deer in Nevada. Jour. Wildl. Mangt., vol. 9, no. 2, p. 145-151. Association of Official Agricultural Chemists 1945. Official and tentative methods of analysis. Assoc. Official Agric. Chem., Wash- ington, D. C, 932 p. Atwood, Earl L. 1948. A nutritional knowledge shortcut. Jour. Wildl. Mangt., vol. 12, no. 1, p. 1-8. Davenport, La Verne 1939. Results of deer feeding experiments at Cusino, Michigan. 4th No. Amer. Wildl. Conf., Trans, p. 268-274. Einarsen, Arthur S. 1946. Crude protein determination of deer food as an applied management tech- ?ii(|ue. 11th No. Amer. Wildl. Conf., Trans, p. 309-312. Ferrel, Carol M., and Howard Leach 1950. Food habits of a California deer herd. Calif. Fish and Game, vol. 36, no. 3, p. 235-240. Forbes, E. B., L. F. Macy, A. LeRoy Voris, and C. E. French 1941. The digestive capacities of the white-tailed deer. Jour. Wildl. Mangt., vol. 5, no. 1, p. 108-114. M ti;iti\ i; \ am I OF FOB \<;i; PLANTS I i D Gordon, Aaron, and Arthur W. Sampson 1939. Composition of common California foothill plants a a factor in range management, Univ. Calif. Agr. Exp. Sim., Bull, 627. Guilbert, II. R. 1942. Some endocrine relationships in nutritional reproductive failure, Jour. A n i ma 1 Sci., vol, I , no. I , p. 3-13. Hellmers, Henry 1940. A study <>( monthly variations in the nutritive value of several natural winter deer foods. Jour. Wil, p. 315-325. I pold, A. S.. T. Riney, R. McCain, and L. Tevis, Jr. 1951. The Jawbone deer herd. Calif. Div. Fish and Game, Game Bull. I. 139 p. Maynard, I.. A.. Gardiner Bump, Roberl Darrow, and J. C. Woodward lit.".."). Food preferences and requirements of the white-tailed deer in New York State. N. Y. Cons. Dept. and X. Y. State Col. of Agr., Bull., no. I, 35 p. Morrison, F. B. L949. Feeds and feeding (21st ed.). Ithaca, X. Y., Morrison Publ. Co., p. 78-95, L80-182, 1086-1087. Nichol, A. A. 1938. Experimental feeding of deer. Univ. Ariz., Tech. Bull., n<>. 7.">, :','.> p. Reynolds, Hudson G., and Arthur W. Sampson 1943. Chaparral crown sprouts as browse for deer. Jour. Wildl. Mangt., vol. 7. no. 1, p. 119-122. Swift, R. W. 1948. Deer select most nutritious forage. Jour. Wildl. Mangt., vol. 12, no. 1. p. 109-110. STUDIES OF BLACK-TAILED DEER REPRODUCTION ON THREE CHAPARRAL COVER TYPES' By RICHARD D. TABER College of Agriculture, University of California, Berkeley INTRODUCTION In August, 1948, a study concerning the effects of chaparral manage- ment on populations of the Columbian black-tailed deer (Odocoih us ht mi- onus Columbia mix) was undertaken. At present this project is still in progress. The work has centered in the region lying just west of Lakeport, California. In this area the hills above about 1,500 feet are covered with a mixture of woody shrubs which are adapted to repeated burning. The three dominant species all crown-sprout after burning ; they are chamise (Adenostema fasciculatum) which grows principally on south and easl slopes, interior live oak (Quercus wislizenii) and eastwood manzanita (Arctostaphylos glandulosa) , both of which grow principally on north or west slopes. These three species make up a little less than half of all the brush cover. About 18 other shrubby species make up the remainder. At the beginning of the study three 1,000-acre study areas were se- lected. Each study area represented one of the three following chaparral cover types attainable by management : (A) opened chaparral, where the brush was interspersed with annual vegetation on some slopes, while scattered patches of heavy unburned brush remained on others; (B) wildfire burn, where the area was swept by a summer wildfire in 1948, with some unburned islands remaining; (C) heavy chaparral, unburned for six years or more. Later another heavy chaparral area (D) was added because part of Area C was burned in 1949. The general region and the location of these study areas are shown on the map, Figure 1. The study areas were selected with the aim of having them as nearly alike as possi- ble, since it was the effects of the cover differences upon the different deer populations that were being investigated. A discussion of these three chaparral cover types in relation to management has been previously presented (Biswell, et aJ., 1952). Figures 2-4 illustrate their general ap- pearance. 1 Submitted for publication July, 1952. Federal Aid in Wildlife Restoration Act, Project California W 31-R. A portion of a thesis in Vertebrate Zoology presented in partial fulfillment of the re- quirements for the degree of Doctor of Philosophy at the Museum of Vertebrate Zoology, University of California, Berkeley. (177) 178 CALIFORNIA FISH AND GAME FIGURE 1. Region of study in Lake County, California BLACK-TAILED DEER REI'KODl < TION 17'' ■ FIGURE 2. Opened chaparral of study area A, Lake County, California m FIGURE 3. Eighteen-month-old wildfire burn of study area B, Lake County, California 180 CALIFORNIA FISH AND GAME •Effete FIGURE 4. Heavy chaparral of study area C. Lake County, California During the months of Februaiy to May, 1950, 38 does, 21 months or older, were collected. Thirteen were from A-type range, 13 were from B-type range and 12 were from C-type range. Because this country is largely roadless the collections involved considerable labor. This was shared by the following Bureau of Game Conservation personnel: Nathan Rogan, then game manager, Merle Sturgeon and Jack Beer, all of the North Coast District, and Alvin Hightower, then of the Disease In- vestigations Laboratory. In addition, William Longhurst and Herbert Hagen, then of the University of California, helped in the collecting. The autopsy work was done by Merton Rosen, Arthur I. Bischoff and John Azevedo, of the Disease Investigations Laboratory of the Bureau of ( Winn' ( lonservation, and Marietta Voge, of the University of California. Many of the ovary examinations which form part of the basis of this re- port were made by Eaymond Dasmann, of the University of California, under the supervision of 0. P. Pearson. Most i.f the does collected carried fetuses. These and the ovaries were preserved at the time of autopsy for future examination. In addition, the skull of each doe was saved for age determination. Mature does were classed as medium or did, the criterion being the state of the occlusal sur- face <»f the lower first molar. If cusps were present the doe was called medium; if the tooth surface was smooth she was called old. .\ study of 1I1 is material east light on the following points concerning the ,|(,es of e;ie|, ;irea : (1 ) age at first breeding; (2) prenatal fawn mor- tality: (3 average fawn production by does of each age class; (4) the date of breeding. AGE AT FIRST BREEDING Studies in New York by Cheatum and Severinghaus (1950) on the Virginia white-tailed deer (0. v. virginianus) indicate that on good range does often breed at the age of seven months. However, in Utah Robinette BLACK-TAILED DEER REPRODUCTION 181 and Gashwiler ( L950) f d thai only 2.2 pereenl of the Rockj Mountain mule deer (0. /'• /" m minis | l';i\\ us would bn ed a1 six to eighl months "I age. In the present study Eour doe fawns have been examined, three ol them being from good range. In noi E them was there any evidence i<> show that their ovaries produced ova during their firsl fall; a little ovarian activity was indicated by the presence of very small Collides. This suggests that under our conditions the breeding of six-month-old docs must be rare or nonexistent. That occasional individuals mighl breed a1 tli is early age is indicated by the records of five black-tailed does which ;it the age of about one year gave birth to fawns. (Rampont, 1926 ; Shantz, 1943.) It is generally thought that- black-tailed does first breed ;d aboul 1*3 months of age. All yearling (18-23 months old) does taken in this collec- tion showed considerable ovarian activity. However, not all of them were pregnant. Two yearling does were taken in A-type (opened brush l range ; each carried one embryo. Three yearling does were taken in B-type (wild- fire burn) range; two carried one embryo each but the third had none. This third doe showed no evidence of ever having been pregnant. No yearling does were collected in the heavy brush (C). These findings bear out the common supposition that a doe's first Hint- ing usually results in a single fawn. In addition, we see here evidence that not all does breed successfully as yearlings. Utah studies have shown that healthy yearlings produced only 0.57 fawns per doe. About one- quarter of them produced twins; over 40 percent of them did not bear fawns (Robinette and Gashwiler, 1950). It cannot be assumed that every yearling doe will bear a fawn. Varia- tions between deer herds in this respect could cause major differences in the relative productivities of the herds. FAWN PRODUCTION OF DOES OF EACH AGE CLASS The fawn production of a given deer herd cannot be learned by simply shooting a sample of does and counting the fetuses unless the sample con- tains the same proportion of yearling, medium aged and old does as is found in the herd. In practice, a sample is apt to be very light in year- lings. This is because the collectors, to avoid collecting fawns, tend to shoot the full grown animals. In the region where this study took place the proportion of yearling does in a herd in the late winter may be most accurately determined by a herd composition count made following the preceding rut. In these counts the medium and old does are lumped as adults. In order to derive the relative proportions of does in the medium and old class it has been as- sumed that these two age classes appear in the collection in the same pro- portion as they occur in the herd. The proportion of these three age classes of does is derived for three study areas in Table I. Having broken down the doe herd of each area into its three component age-classes, we must now discover the fawn production of each class. For does which were pregnant when collected it is easy to derive the average number of fetuses per doe. However, some of the does in this collection had already dropped their fawns. Only by studying their ovaries could one discover how many fawns each had produced. 182 CALIFORNIA FISH AND GAME TABLE 1 The Derivation of the Percent of Does in Each of Three Age Classes on Three Chaparral Cover Types, 1950 Area A (opened brush) Area B (1948 wildfire) Area D (mature brush) Percentage of breeding doe population made up of 18-23 month old 9 9 according to 1949 herd composition count 26 33 27 Percentage of does over two years old in each of two classes, medium and old, based on proportions taken in 1950 spring doe collection medium 64 old 36 medium 70 old 30 medium 64 old 36 100 100 100 Percentage of doe population made up respectively of year- ling, medium and old does (based on above) yearling 26 medium 47 old 27 yearling 33 medium 47 old 20 yearling 27 medium 46 old 26 100 100 100 "When a doe comes into heat and. her ovaries discharge one or two ova, the ruptured follicles from which these ova came are then filled by en- larged cells and so form solid bodies called corpora lutea. If the ova are not fertilized the corpora lutea begin degeneration after 14 to 15 days. On the other hand, if the ova are fertilized the corpora lutea persist throughout the period of gestation and for some months thereafter (Cheatum, 1949). These corpora lutea may easily be seen with the naked eye ; if the fresh ovary is sliced with a razor blade each corpus lutem of pregnancy appears as a solid yellow ball. Since two ova may be shed at the same time, but only one of them fer- tilized, it is not accurate to regard the total number of corpora lutea as '•oiTesponding exactly to the total number of fetuses. It is necessary to compare the total numbers of corpora lutea and fetuses appearing in those does which were pregnant when collected and then apply this ratio, the "fertilization-rate" to those does which had already fawned when TABLE 2 Fertilization Rates According to Chaparral Cover Type and Doe Age Class Chaparral cover Age class Total number of animals in class Total number of corpora in class Total number of fetuses in class Fertilization rate •:ned brush j A (opened brush) A (opened brush) Yearling Medium Old 2 6 3 2 11 6 2 10 5 100 91 83 B l'< 18 wildfire) B (1948 wildfire) B (1948 wildfire) Yearling Medium. Old... 3 .5 3 2 9 5 2 9 4 100 100 80 C (heavy brush) C (heavy brush) Medium Old 2 2 1 3 1 3 100 100 Total 39 Weighted average 94 BLA< K TAILED DBEH REPR0D1 OTION l-:; I hey were collected. This has been done in Table 2. Thus the terra fertili zation rate" used in Table 2 refers to the proportion of the oumber of refuses In the number of corpora Lutea. It has been found among the deer herds of New York to v;iry from 68 to 96 percent (5) and in OUr deer collection to vary from 80 to LOO percent, with an average of "1 percent. Evidently 6 percenl of all ova shed al the time of successful breeding did qo1 develop into fetuses. These ova were either no1 fertilized a1 all, or were fertilized bu1 did nol survive. It is of interest to note thai there seems to be some tendency toward ;i lower fertilization rate among the older does. This means thai of the ova which these older does shed, relatively fewer developed successfully into fetuses. In spite of this tendency the old does averaged bighesl in fawn production on two of the three study areas. Among the mule ilcrv of Utah it has been found thai the fawn produc- tion of very old does is lower than that of prime dues (Robinette and Gashwiler, 1950). This is not necessarily in conflict with the findings of the present study. Because of the way our ape classes have been setup we include in our "old" class some deer which in Utah would be regarded as "prime." This has resulted, in our case, in the masking of the decline in productivity which probably accompanies extreme old age. Having seen that 94 percent of all the shed ova were fertilized and de- veloped to the point where they were easily recognized by the naked eye, we have next to see whether there was any loss, or abortion, bet ween that point and birth. Altogether 50 fetuses were taken from collected does. Each one was carefully examined. All of them seemed to have been alive and healthy up to the moment of the doe's death. Under our conditions, then, abortion seems not to be an important factor in reducing the fawn crop. This is in agreement with the findings of Robinette and Gashwiler (1950) in the mule deer of Utah ; out of 318 fetuses they found only three (0.9 percent) which were abortive. By applying the data on "fertilization-rate" from Table 2 to the does which had already fawned when they were collected, their fawn produc- tion can be calculated. The records of these does are added to the ones for which fawn production was previously determined, to give the fawn production within each of the three age classes on the three areas of different brush condition. These averages are given in Table 3. TABLE 3 The Fawn Production Within Each of Three Age Classes on Three Chaparral Cover Types Chaparral cover type Number of does Age class Total number of fetuses Average number of fetuses per doe (A) Opened brush ._ __ ._ 2 7 4 Yearling Medium . . Old 2 11 7 1.00 (A) Opened brush 1.57 (A) Opened brush __ 1.75 (B) Wildfire burn... 3 7 3 Yearling Medium _. Old 2 10 4 0.66 (B) Wildfire burn . 1.43 (B) Wildfire burn __ 1.33 (C) Mature brush 8 4 Medium Old. 7 4 0.88 (C) Mature brush 1.00 184 CALIFORNIA FISH AND GAME It may be recalled that no yearling does were collected in the mature brush (C) area. Since the productivity of the medium and old does in this area is lower than that of similar does from the other areas, it seems probable that the productivity of yearling does in the mature brush is lower than the productivity of yearling does in the other areas. There- fore I shall assume an average of "less-than-0.66" fawns per doe as the production of the yearling does in the heavy brush. The average number of fawns per doe, from Table 3, may be multi- plied by the percent of breeding does in each age class, from Table 1, to give the productivity of that class. This is done in Table 4. TABLE 4 Average Fawn Production of Breeding Does on Three Chaparral Cover Types Chaparral cover type Age class Percent of Average Fawn breeding does number of production in this age fetuses per of this class doe in this age class age class (A) Opened brush Yearling Medium Old.. 26 X 1.00 = 26.0 (A) Opened brush __ ._ _ - (A) Opened brush , _ _ 47 X 1.57 = 73.8 27 X 1.75 = 47.2 147.0 fawns per 100 breeding does (B) Wildfire burn _ .... Yearling _. Medium.. . Old 33 X 0.66 = 21.8 (B) Wildfire burn.. 47 X 1.43 = 67.2 (B) Wildfire burn... .. 20 X 1.33 = 26.6 115.6 fawns per 100 breeding does (C) Mature brush. .. Yearling Medium Old Less than Less than 27 X 0.66 = 17.8 (C) Mature brush . . 46 X 0.88 = 40.5 (C) Mature brush. . . . . 26 X 1.00 = 26.0 less than 84.3 fawns per 100 breeding does Table 4 indicates that fawn production is highest in the opened brush (147 per 100 breeding does), intermediate in the wildfire burn (115.6 per 100 breeding does), and lowest in the mature brush (less than 84.3 per 100 breeding does). DATING THE RUT Each fetus was aged by means of Armstrong's key (1950). Since this key employs combinations of developmental characters, such as appear- ance of hair, pigment spots, eyelashes, etc., it is sometimes not possible to age a fetus precisely ; in such a case it may be said that the fetus is within a certain range of ages. The midpoint of each such range was taken as the true fetus age. The age of each fetus may be subtracted from the date of collection to give the date of conception. So far as can be determined 1 1 1 . \ c ■TAILED hi.i.i; i;i ,i-i;< >l>r< ITION i-:. the docs in all three study areas bred ;it aboul the same time. The peak of conception Eor L949 was aboul the last week of October and the first two weeks of November. The dates of conception for all three areas are combined in Fierure 5. October November December FIGURE 5. The time of breeding (1949) for 37 block-tailed does From Figure 5 it is evident that yearling does bred later than the average of older does. Also the medium aged does tended to breed at the peak of the rut, while the old does formed the most erratie class, breed- ing both early and late. The observation that yearlings tend to breed late is commonly made among livestock. In New York (Cheatum and Morton, 1946), where fawns often breed, it has been found that their average breeding date falls about a month later than that of the older does. DISCUSSION The evidence here reported points to the conclusion that the three groups of deer under study had different reproductive rates. Since each group of deer was from a different chaparral cover type, it is logical to inquire whether the differences in vegetative cover might not account for the differences in productivity. To clarify the relationships between cover, nutrition and reproduction it is necessary to investigate deer diets and the nutritional values of these diets. Such a studv is now under wav. SUMMARY This report is based on a collection of does made on three contrasting chaparral cover types in Lake County, California, during the months of February, March, April and May, 1950. These cover types were: (A) opened brush (interspersed with herbaceous cover) ; (B) a 1948 wild- fire burn ; ( C ) mature brush. It was found that these deer probably 186 CALIFORNIA FISH AND GAME rarely or never breed as fawns, but commonly first breed as yearlings (at about 17 months). On some ranges not all yearlings breed. Ovary studies showed a ' ' fertilization-rate " of 94 percent. No evidence of pre- natal fawn mortality was found. The rates of fawn production were found to be: (A) yearlings, 100 percent; medium-aged does, 157 per- cent; old does, 175 percent; (B) yearlings, 66 percent; medium-aged does, 143 percent; old does, 133 percent; (C) yearlings (none collected), assumed to be less than 66 percent ; medium-aged does, 88 percent ; old does, 100 percent. The total productivity of the breeding doe herds was found to be: (A) 147 percent; (B) 115.6 percent; (C) less than 84.3 percent. The peak of conception was found to be the last week of October and the first two weeks of November. The yearlings bred late, the medium- aged does toward the center of the period and old does bred both early and late. LITERATURE CITED Armstrong, R. A. 1950. Fetal development of northern white-tailed deer (Odocoileus virginianus lorealis Miller) . Amer. Midland Nat., vol. 43, no. 3, p. 650-666. Biswell, H. H., R. D. Taber, D. W. Hedrick and A. M. Schultz 1952. Management of chamise brushlands for game in the north coast region of California. Calif. Fish and Game, vol. 38, no. 4, p. 453-484. Cheatum, E. L. 1949. The use of corpora lutea for determining the ovulation incidence and varia- tions in the fertility of white-tailed deer. Cornell Vet., vol. 39, no. 3, p. 282- 291. Cheatum, E. L., and G. H. Morton. 1946. Breeding season of white-tailed deer in New York. Jour. Wildl. Mangt., vol. 10, no. 3, p. 249-263. Cheatum, E. L., and C. W. Severinghaus. 1950. Variations in fertility of white-tailed deer related to range conditions. 15th No. Amer. Wildl. Conf. Trans., p. 170-190. Morton, G. H., and E. L. Cheatum. 1946. Regional differences in breeding potential of white-tailed deer in New York. Jour. Wildl. Mangt., vol. 10, no. 3, p. 242-24S. Rampont, R. O. L926. Black-tailed deer successfully raised. Calif. Fish and Game, vol. 12, no. 1, p. 35-37. Robinette, W. Leslie, and Jay S. Gashwiler. 1950. Breeding season, productivity and fawning period of the mule deer in Utah. Jour. Wildl. Mangt., vol. 14, no. 4, p. 457-469. Shantz, II. L. L943. Sexual maturity of deer. Hearings before the Select Committee on Con- servation of Wildlife Resources, Seventy-eighth Congress, p. 288. A POSSIBLE METHOD OF INCREASING WESTERN MOUN- TAIN MAHOGANY ON GAME RANGES1 By H. H. BISWELL, A. M. SHULTZ, and D. W. HEDRICK School of Forestry, University of California, Berkeley Western mountain mahogany (Cercocarpus b&tuloides) is one of the better browse plants in Calif ornia, and is cropped readily by deer, sheep, and cattle. This shrub or small tree is scattered in the fool lulls and moun- tains ;if elevations between 500 and 4,000 feet throughout California west of the main Sierra crest. It may be five to eighl feet high with spreading branches, or it may form a small tree up to 20 fool high (Jep- son, 1925). Western mountain mahogany is one of the main browse spe- cies for deer in the regions of the north Coast ranges, the south Coast ranges, the west slope Sierra, and Southern California (Longhurst, Leopold, and Dasmann, 1!).V2). In most areas a greater abundance of this species would be desirable for door browse and it seems the plant should be increased if possible, especially at the expense of some of the lesser browsed species snob as the manzanitas. Observations and limited measurements made in the foothills of Madera County indicate how western mountain mahogany might be in- creased in abundance. A few scattered trees of this species were heavily laden with ripe seeds just prior to a control burn of brush on -Inly 17. 1949. The trees were 14 to 16 foot high on a north-facing slope. The tire. burning up the slope, was intense enough to kill the trees and other shrubs, but it did not destroy the seeds on the trees. Three days after the tire the soil in this area was densely covered with mahogany seeds. Early in the summer of 1950 a large number of mountain mahogany seedlings were found in the area, in some places as many as six or seven per square foot. Many of these survived the summer drought period. On July 20, 1951, two years after the control burn, the seedlings on four plots were counted. Each plot had a radius of nine feet. There were 12, 21, 4!) and 248 seedlings on these plots, with an average of one two- year-old seedling per three square feet. A majority of tin1 seedlings ap- peared healthy, with maximum heights in the plots between six and 12 inches. The net result was a great increase in western mountain mahogany on this north-facing slope. Inspections of several late summer wildfire burns in Madera County and elsewhere, over a period of four years, revealed no seedlings of western mountain mahogany while seedlings of many oilier shrubs oc- curred in great abundance. It is probable that the seeds will not survive intense summer fires and that they may not remain viable after lying in the duff for long periods of time. The seeds of western mountain 1 Submitted for publication November, 1952. Federal Aid in Wildlife Restoration Act, California Project W-31-R. (187) 188 CALIFORNIA FISH AND GAME FIGURE 1. Twig from western mountain mahogany laden with ripe seeds. The live twig was eight inches long. WESTERN MOUNTAIN MAHOGANY l"'1 mahogany have a soft coat, unlike those of ninny other shrubs. Rodents may ea1 many of the seeds. In the absence of fire a few seedlings emerge each year in the vicinity of old plants but many of them die the first summer after germination as a result of severe plant competition. Nevertheless, this is the prin- cipal way in which the plant increases in abundance. Western mountain mahogany sprouts vigorously alter a fire. On Bum- mer ranges the new sprouts may he browsed so heavily that some of the plants are killed. <>n winter ranges, however, utilization may not be particularly heavy or damaging because the shrub is largely deciduous and most of the leaves have fallen. Based on the above observations, it would appear that controlled fires might be used in some instances to increase the abundance of western mountain mahogany. If this is attempted the firing should be restricted to years of heavy seed crop, when the seeds are nearly ripe and before they fall. The ideal fire seems to be one intense enough to kill the moun- tain mahogany trees and other shrubs but not so severe as to injure the seeds on the trees. These results are part of the investigations being carried on coopera- tively between the I'niversity of California and the California Depart- ment of Fish and Game with funds provided by Federal Aid in Wildlife Restoration Act, Pittman-Robertson Research Project California W-31-R. LITERATURE CITED Jepson, W. I.. 1925. Manual <>f the flowering plants of California. Berkeley, Univ. Calif.. Asso- ciated Students Store, 1238 p. Longhurst, William M., A. S. Leopold and R. P. Dasmann 19">2. A survey of California deer herds, their range and management problems. Calif. Dept. Fish and Game, (lame Bull. 0, 130 p. PROGRESS REPORT ON A STUDY OF THE KELP BASS, PARALABRAX CLATHRATUS* By ROBERT D. COLLYER and PARKE H. YOUNG Marine Fisheries Branch, California Department of Fish and Game INTRODUCTION Five species of lisli are particularly important to ocean anglers in Southern California. These are, iu 1 1n* probable order of desirability, albacore (Thunnus germo), yellowtail (Seriola dorsalis), white seabass (Cynoscion noMUs), barracuda (Sphyraena argentea) , and the kelp bass (Paralabrax clathratus). The kelp bass, though not the most desirable, is probably the most important of the game fish in Southern California, because it is available during the entire spring to fall fishing season. This small fish is excellent eating and has fine fighting qualities. More kelp bass are landed by the extensive sportfishing fleet than albacore, yellow- tail and white seabass combined. Currently, the department is conducting extensive studies of the alba- core and yellowtail. The white seabass and barracuda have been the objects of moderate studies in the past. The kelp bass, however, had received limited attention. Consequently, as part of the departmental over-all program to benefit marine recreational fishing, it was selected as the species most in need of comprehensive life history study. The work upon which this report is based was started in 1950. It has consisted largely of a tagging program from which information on growth, migration and spawning activities has been gathered. In addi- tion, the catch of bass per angler each year has been determined from the daily records maintained by sport boat operators. While it is still too early to draw conclusions, it seems wise to present these preliminary results because of the widespread interest of sportsmen in the kelp bass fishery and in this investigation. There are three species of Paralabrax which are lumped together on the daily catch records. The kelp bass is by far the most important. How- ever, the average sportsman does not distinguish between it and the sand bass (P. nebulifer). The spotted bass (P. maculatofasciatus), the third species, is an inhabitant of the bays and lagoons and is uncommon in the angler's bag. Except for the tables giving records of fish tagged and re- covered, this report deals with the kelp bass alone. Many of the authors of manuals dealing with marine sportfishing in Southern California have devoted some space to the kelp bass : one of the interesting features is the increasing importance of the species. In 1912, Holder wrote that the kelp bass is a "small fish to be caught in unlimited quantities . . . though to the yellowtail or white sea bass angler it is considered a nuisance.'3 In 1930, Thomas referred to the kelp bass 1 Submitted for publication November, 1952. (191) 2 — 71944 192 CALIFORNIA FISH AND GAME "... affords much pleasure to those who do not care to venture far to sea." These examples trace in a popular sense the transition from a ' ' nuisance " to a " pleasure. ' ' In recent years, the kelp bass has provided more fish per sport boat angler than any other species. However, it is very doubtful that the average weight of the fish this day would be half that of the kelp bass in 1912. CATCH RECORDS All boat operators who take paying passengers fishing are required to keep records of their catch. Figure 1 is a graphic picture of the total kelp bass catch during May and June for the years 1936-1951 as indi- cated by the daily catch records of the many sport fishing boats that 280 1 ■ — . 260 240 220 5 200 o ir ieo ^ D O 160 V) s < z II YEAR AVERAGE CATCH ** 140 =- — : >- < O I .20 W 2 OE X ' Ui u. — — Ul D 5 80 60 40 — 20 o — — « Kl K» O>Ol0f-CDl7>O — FIGURE 1. Number of Paralabrax landed by recreational fishermen, Los Angeles and Orange Counties, May and June only. The horizontal line is the 11-year catch average. Number of fisherman-days indicated by shaded areas. (Numbers are in thousands.) STUD'S OP THE KELP U \ 193 operate in Southern California. The lower pari of each bar indicates the number of fisherman days involved in the catch for the two months. These two months were selected because at this time sportsmen are most con- sistently fishing Eor kelp bass. In other months bass fishing is often af- fected by occurrences of albacore and other species which are soughl in preference to kelp bass. FIGURE 2. Paralabrax. catch per angler-day, Los Angeles and Orange Counties, May and June only. The trend lines are fitted by the least squares method. Figure 2 interprets the trend of the kelp bass fishery in terms of fish per angler-day. There are many factors that determine the trend, which over a long period of time, tend to balance out. No data were available during the war period. The trend lines are calculated from the data gathered from a wide area, from Point Dume above Malibu Beach to a point several miles south of San Clemente and from the islands of Santa Catalina and San Clemente. Catch trends from limited areas vary con- siderably. The slopes of the lines for the periods 1936-1940 and 1946- 1950 are very similar and indicate a rapid decline. For the latter time interval, however, this downward slope results from the high return in l!»4(i immediately following the curtailment of sport fishing during the war years. A line fitted to the years 1946-195] has a lessened decline and if a line were fitted to the records for 1947-1951 there would be an up- ward trend. Presumably the stocks of bass accumulated on the fishing grounds between 1940 and l!)4(i because of lessened fishing effort. These were quickly reduced in numbers but have held their own since 1!»47 with indications of a slight recovery. As indicated in the following discussion not all grounds have been fished with equal intensity. Pishing effort on local grounds varies from season to season and the upward trend in re- turn may result from concentration of fishing on less exploited localities. A more detailed analysis of catch records, now in progress, should give more accurate information about the abundance of bass stocks on the many fishing grounds. 194 CALIFORNIA FISH AND GAME SIZE OF FISH ON DIFFERENT FISHING GROUNDS On the fishing grounds that are readily accessible to the large number of party boats in Southern California a reduction in the length and weight of the kelp bass taken by angling has been evident. On some of the very old fishing grounds, kelp bass have all but disappeared from the angler's bag. In other areas, such as the coastal section between La- guna Beach and Oceanside, exploitation of an intense nature has started since the end of the war. At the beginning of this exploitation, the kelp bass were largely of the size known as "bull" bass which can be com- pared to a ' Hunker" when speaking of freshwater black bass. Following one or two seasons of intensive fishing in this area, ' ' bull ' ' bass were far less common, and the smaller bass maintained the fishery. This trend has continued until, at the present time, bass less than 11 inches in length comprise 75 percent of the catch. San Clemente Island fishing offers a similar example of the sharp decline in size of the kelp bass. The length frequency distributions of bass, caught by hook and line, at five well separated areas (Figure 5) suggests that the number of large kelp bass are closely related to fishing effort. For instance, the Santa Cruz Island fishery has been exploited by several sportfishing boats operating out of Port Hueneme. These boats do not operate daily, and the fishing season is not as long as the season farther south. The bass at Santa Cruz Island are large by the sportsmen's standard, averaging 15^ inches total length. At San Clemente Island, a fishing grounds that has been quite popular fol- lowing the war, the kelp bass now approximate 14 inches in total length. San Clemente Island is accessible to boats operating out of Los Angeles Harbor, Long Beach, and Newport Beach. A further comparison of the length frequency distributions of Santa Cruz Island fish with those from San Clemente Island shows that Santa Cruz Island has a greater reser- voir of large bass, and that the percentage of each size group is more in balance. The highest mode for San Clemente Island occurs at a point slightly above 12 inches. For Santa Cruz Island, the highest mode occurs at approximately 14^ inches with two additional modes of nearly the same strength at 16 and 18-| inches. At Santa Catalina Island, for the years 1950 and 1952, length fre- quency distributions differed widely from those at both San Clemente and Santa Cruz Islands. Kelp bass at Santa Catalina Island have been the object of a continuing fishery for several decades. The shoreline to a depth of 60 feet is well populated with bass, some localities more heavily than others. However, bass 12 inches or longer form less than one-third of the catch. Contrast this with Santa Cruz Island and San Clemente Island where 9 out of 10 bass exceed 12 inches in length. Occasionally, kelp bass over 18 inches total length are taken at Santa Catalina Island, but this is uncommon. The extensive Santa Catalina shoreline with its numerous hays and inlds provides cover for a portion of the bass population. An area less fortunate in protective cover would have even fewer large bass. The fishing grounds near the mainland town of San Clemente offer a good example of an area that does not provide ample escape cover. These grounds have been heavily exploited since 1946, and the length frequency distribution of the 429 fish tagged there reflect this exploitation. The mode is located at 9.5 inches, dangerously close to the point at which the kelp ltriss reaches first maturity. There seems to be no reservoir of large ST1 l>Y OF THE KELP R \.~- 195 fish, and tlic steep ascending curve would indicate thai small kelp ba just beginning to enter the sporl fishery, form a substantia] pari of the catch. The S;m ( 'Icinciiic fishing grounds include those off San Onofre and Las Flores. The boats that operate in this area are based at Newporl I leach and at San ( 'leinente. Pish from a Long, dense bed dl' kelp between La Jolla and Poinl Loma, principally known as the La Jolla kelp beds, present a length frequency distribution with a higher proportion <>)' lame bass than off the town of San ( 'leinente. There are at least two basic reasons for this. The I, a .Jolla beds are fished by boats from San Diego, but mostly as a second choice location, the Coronado Islands being preferred. Secondly, the extent of the kelp beds offers protection to the fish as well as being an inhibiting factor to the passage of small boats. TABLE t Number of Kelp Bass Caught by Size— Hook and Line Fish Only Area Size in inches 6-8 8-9 9-10 10-11 11-12 12 plus Santa Catalina Island, 1950 24 8 0 0 2 5 47 84 0 4 34 12 79 100 0 2 117 37 87 95 1 14 124 83 48 84 7 14 70 81 117 Santa Catalina Island, 1952 148 Santa Cruz Island, 1950 1 50 San Clemente Island, 1950 . San Clemen te (Town), 1950_ La Jolla, 1950 198 32 123 TABLE 2 Percentage of Kelp Bass Caught by Size — Hook and Line Fish Only Area Santa Catalina Island, 1950 Santa Catalina Island, 1952 Santa Cruz Island, 1950 San Clemente Island, 1950_. San Clemente (Town), 1950 La Jolla, 1950 Size in inches 6-8 5.97 1.52 0 0 .52 1.46 8-9 11.69 16.00 0 1.72 8.97 3.51 9-10 19.65 20.19 0 .86 30.87 10.85 10-11 21.64 18.09 .63 6.03 32.71 24.34 11-12 11.94 16.00 4.43 6.03 18.46 23.75 12 plus 29.10 28.19 94.3 85 . 34 8.44 36.07 Tables 1 and 2 present a convenient breakdown of the length frequency distributions from the five areas under discussion. These tables permit comparison of one area with another, particularly on a percentage basis. They are also valuable in determining the result of a limitation of catch (size limits), if any such limitation were to be instituted. These tables are based on hook and line caught fish only. 196 CALIFORNIA FISH AND GAME TAGGING Localities To determine the amount of movement, kelp bass have been tagged ex- tensively. Tagging operations during 1950 and 1951 were spread from the Channel Islands and Point Dume to San Diego in California waters. Tagging also took place in Baja California, mostly from the research vessels operated by the Department of Fish and Game. During the 1952 season, tagging was concentrated at Santa Catalina Island and at La Jolla on the mainland. A sprinkling of fish was released in Mexico. During the three seasons concerned in this report, a total of 3,980 bass was tagged and released over a large area of the Southern California seacoast. In Mexico, 192 bass were tagged and released. Figures 3 and 4 show the number and the approximate locations of the tagged fish in both of these large areas. SAN NICOLAS IS. LA JOLLA FIGURE 3. Distribution of 3,980 iagged kelp bass in Southern California; fish were tagged during the 1950, 1951 and 1952 seasons Recovery Rates Kelp bass were captured for tagging by hook and line, and also by trapping. The tags were attached to the fish with silver wire, stainless steel wire and by monofilament nylon. The recovery rate of bass caught by hook and line is slightly better than that of trap caught fish. Recoveries of bass tagged with nylon tend to be higher than are the returns of bass tagged with either silver or stainless steel. STUDY OF 'I'll i; KELP BASS l!i" a© UGUADALUPE IS FIGURE 4. Distribution of 192 tagged kelp bass in Baja California Table 3 presents the number of fish tagged and the number returned by area. Table 4 is derived from the rate of tag recovery by month. Table 5 represents the number of bass tagged by species, and the recovery by species. Over half of the 506 recoveries, kelp bass and sand bass, were received within the first month and 75 percent were made within the first 60 days. The rapidly declining rate of return indicates quite strongly that there is a tag loss of some proportion. At the same time, the rapid rate of return also indicates a heavy fishing mortality in the areas where tagging took place. On the San Clemente-Las ETores fishing grounds, there was a total tag recovery of 26 percent despite apparent tag h>sv. This high return correlates with the small number of large bass in the same area. Nineteen percent of the bass tagged at San Clemente Island during 1950 were recovered. There has been no attempt to tag bass here during 1952. However, if an appreciable number of kelp bass were tagged 198 CALIFORNIA FISH AND GAME during 1952, it is very doubtful that the tag* recovery would have ap- proached 19 percent. The explanation of this statement lies in the fact that the runs of barracuda, yellowtail and albacore were of large pro- portions on local grounds during 1952 and the long voyage to the island was unnecessary. TABLE 3 Releases and Recoveries of Tagged Kelp Bass, 1950-1952 — California Only Number released Number recovered Area 1950 1951 1952 Total 1950 1951 1952 Total 93 49 22 9 381 1 13 310 235 90 311 117 15 4 19 67 6 30 108 37 13 1,085 4 3 3 955 210 49 37 13 19 1,533 7 47 421 275 90 1,279 1 2 2 58 1 10 74 43 13 42 1 1 1 13 3 36 10 1 1 142 1 34 1 3 Point Dume-Malibu - - --- 1 3 San Nicolas Island - _ 213 1 Newport Beach-Dana Point 13 111 San Clemente Island -___ __. ._ 53 14 La Jolla-Point Loma _ __ _ 77 Totals -. .- -----_ .. -- 1,514 416 2,050 3,980 246 67 177 490 TABLE 4 Recoveries of Tagged Kelp and Sand Bass From California and Baja California Time out in months 0-1 1-2 2-3 3-4 4-5 5-6 6-7 7-8 8-9 9-10 10-11 11-12 12-13 22-23 Number returned* 258 123 47 24 5 2 1 0 2 4 3 6 1 1 Percent returned 54 26 10 5 1 .4 .2 .4 .8 .6 1.3 .2 .2 * An additional 29 fish were returned without information as to the date of recapture. TABLE 5 Releases and Recaptures by Species California and Coronado Island South of Coronado Islands Kelp bass Sand bass Kelp bass Sand bass Spotted bass 3,980 26 192 215 21 Number returned 490 3 10 3 12.3 11.5 5.2 1.4 STI HV OP THE KELP B \.— I'l'i i — i — i — i — i — r SAN CLEMENTS TOWN 1940 I I I I I I I ^S ,' v, SAN CLEMENTt ISLAND 1950 J I •>-<\b^J •k I 8 50 52 54 56 58 60 FIGURE 5. Kelp bass length frequency distribution from five of the principal fishing grounds The tag recovery rate of 14 percent at Santa Catalina Island indicates a fairly heavy effort. This island constantly supports considerable fishing effort. A large proportion of the yellowtail and barracuda taken during 1952 were caught there. Most of the sport fishing fleet that fishes Santa Catalina Island will, as a matter of course, make its way to the island hoping that barracuda and yellowtail will be there. If they are not, there are always kelp bass, with the chance that white sea bass may be taken. Tag recovery at the La Jolla kelp beds amounted to a total of 6 per- cent. This recovery was a combination of fish that were caught by hook and line fishing and by trapping. The hook and line fish were tagged at intervals between Point Loma and Bird Rock, La Jolla. The trapped bass were tagged and released principally at La Jolla Cove, a few near Bird Kock. 200 CALIFORNIA PISH AND GAME FIGURE 6. Recovery locations. The circled numbers indicate kelp bass migrating five miles or more. The base of the arrows show original tagging locations. MOVEMENT Figure 6 shows the movements of 16 kelp bass that equalled or exceeded a distance of five miles. An additional 23 fish moved from a few hundred yards up To four miles. One bass recovered at Guadalupe Island, Baja I Jalifornia, traveled approximately 17 miles. Twenty-eight fish were re- turned wit]] no data as to movement. A second small block of fish was re- covered with data that were either incorrect or could not be verified. Over 400 of the bass recovered, both in Mexico and California, showed no movement. The results of tag recovery, combined with the striking differences in the length frequency distributions, strongly suggests that the kelp bass fishery is based on a series of independent populations. This belief is fur- t her -1 rengthened by the observations of many boat captains in the sport fishing fleet. These men have noted that specific fishing holes can be, and are often, depleted to the point that minnow-size bass are the rule! The recovery of such a depleted ground would depend upon the growth of the small tisli in the area, with the possibility of an occasional migrant from another area. STI l>Y OF THE I. I.I.I- H \ 201 GROWTH The growth of kelp bass is based upon summer growth data collected From 10 fish thai were al liberty from 16 to 133 days following tagginp The growth data were arranged to determine growth rate following modification of the method advanced by Walford 1946 . Figure 7. To estimate growth rates a 60-day interval was chosen. For the 1" fish the length ;it time of release and of recovery was available. The amounl growth of each fish was divided by the number of days ;ii liberty to obtain the average daily growth rate. This daily average was then multi- plied l»v 60 to estimate the growth over a 60-dav interval. CD er- 560 -J 1 1 1 1 1 1 i \ 1 1 1 1 1 1 1 / 350 -I3.S : 310 330 — 13.0 y% — 320 -12 5 — 310 -12 0 — 300 290 to -0 t- -c i "3 C w * C O CJ 0) ■9 .3 = 1 oj , rH T +^ oj ooon , co 3 s_ o t- , CO S 3 a -^ C £ 2 Ph = CI i to CN fe"? hin BM 'CO o 3 u , g ih i O , , © CN , CO 3 iii — , i u *j CI c3 2 PL, = CI O I- -3 i iu3(» , CN CN I.I £ 3 o 1 1 Tf 1 , i , , , t- CJ , , , , , -O i , , , , o . 4^ 8J ^ i ! ! ! !o C o i ' ' ' ' 0J § April May June July August.. Septemb 204 CALIFORNIA FISH AND GAME observations we would conclude that both rock [sand] and kelp bass spawn during the summer months of June, July and August .... ' ' Presumably the average size at first maturity for the kelp bass is about 25 cm., or 10 inches." Table 6 is arranged from data gathered during 1950 and 1952. In general, the larger fish show evidence of some stage of maturity as early as April. Bass between 201 to 225 mm. are beginning to show signs of maturity in June, and one out of five of the sample of 47 fish taken in July are maturing. In the next size group, from 226-250 mm., three out of four bass are in some stage of maturity during July. All bass larger than 250 mm. would be approximately 100 percent mature by July. In general, the findings of the maturity studies substantiate the con- clusions by Clark. However, some bass, less than 25 cm. were found to be maturing. From the length frequencies of bass taken from heavily fished areas such as Santa Catalina Island, and the town of San Clemente, it is obvious that an appreciable percentage of the fish in the catch have not reached maturity. TAGGING METHODS All the bass were tagged with Petersen disks. The disks were lam- inated with printing on the center layer and protective transparent layers on front and back. Two types were used : 1. 1950 and part of 1951 : cellulose acetate disks, 9/16-inch diameter x .030-inch thick. 2. Balance of 1951 and 1952 : cellulose nitrate disks, ^-inch x .040-inch. This change was made as a result of experiments which showed that cellulose nitrate was superior to cellulose acetate (Calhoun et al . 1951). Three materials were used to attach Petersen disks : 1. 1950 and some in 1952: pure silver, medium hard temper pins, .DlO-inch diameter. 2. 1951 : type 302, soft temper stainless steel pins .032-inch diameter. • l. 1!»52 : monofilament nylon leader material, 20-pound test, diameter about .023-inch but varies according to manufacturer. - ' nher materials used included pointed-nose pliers, hypodermic needles lor inserting the wire or nylon through the fish, a measuring device, recording sheets and, for the nylon leader method, a plastic spacing device. A tagging trip was first arranged with a boat owner. The Southern Council of < Oiiscfvation Clubs was then contacted and it in turn found the required number of fishermen among its member clubs. At the ap- pointed day and hour, the various sportsmen, Department of Fish and . A new graphic method of describing the growth of animals. Biol. Bull., vol. '.10. no. -2. p. 141-147. Thomas. George <"., Jr.. and (r. ( '. Thomas. Ill 1930. Game fish of the Pacific. Phila., J. P. Lippincott, 293 p. AQUARIUM TESTS OF TAGS ON STRIPED BASS By A. J. CALHOUN Inland Fisheries Branch, California Department of Fish and Game Anglers for striped bass (Roccus saxatilis) have increased sharply in California (Calhoun, 1950) and the upward trend is expected to con- tinue. This situation raises questions aboul the adequacy of presenl regulations such as Length of season, bag limit and minimum size. These cannot be answered sensibly without knowing roughly how many of the available fish are being caughl annually. One objective of the California Striped Bass Investigation has been to obtain an index of the presenl rate of harvesl by means of a tagging program. It soon became apparent that a better tag than those used pre- viously on bass (Clark. 1934, 1936; Merriman, 1941) was accessary. Cer- tain metals and plastics commonly employed in the past were Pound to have serious shortcomings (Calhoun, Pry and Hughes, 1951). Extensive tagging of wild fish of many kinds i Rounsefell and Kask, 1!)45) has not ordinarily thrown much light on the relative merits of different kinds of tags or different locations on the fish. Aquarium tests, for all their obvious limitations, can reveal a greal deal along these lines. This report summarizes the results of recent aquarium experiments to discover satisfactory materials for Petersen disk tags and to observe the individual behavior of various kinds of tags in different locations on striped bass over fairly long periods of time. The cooperation of Dr. E. S. Herald. Curator of Steinhart Aquarium, is gratefully acknowledged. He made a Large, salt-water display tank available indefinitely for this project. The tagged fish, shown in Figure 1, became a popular public exhibit. We are also indebted to Messrs. Rob- ert Dempster, Fred Herms. and Walter Schneebeli of the aquarium staff, who cared for the fish. The stimulating suggestions of Mr. Park B. Wydr and his assistance in fabricating special tags were particularly helpful. PETERSEN DISK TAGS The Petersen disk tag still appears to be the most satisfactory type of tag for general use on striped bass. It consists of two buttons, one at each end of a wire passing through some part of the fish. Examples can be seen on the tails and beneath the dorsal fins of the fish in Figure 1. The knot commonlv tied at each end of the wire is shown in Figure 3a. 1 Submitted for publication November, 1952. ( 209 ) 210 CALIFORNIA FISH AND GAME < D _C C '« o c o a o -Q -a o Of O A.QUARIUM TESTS OF TAGS ON STRIPED i:\ -11 Metals and Plastics Ivcccnl studies have beeE aimed primarilj a1 discovering some com- bination of metal wire and Petersen disks which would lasl indefinitely on Large, active fish in sail and brackish water. Nickel, silver, and monel have not been tested further, since they are clearly unsatisfactory (Cal- houn, Fry and Hughes, 1951 >. Worfc with stainless steel has continued. Type )>1(> wire showed no evidence of corrosion or weakening even after two years in the aquarium. Similarly, type 302 wires were uniformly in perfect condition alter M months, when nil of the test fish died as the result of an accident. Further evaluation must await the results of more prolonged tests with wild fish. Testing of tantalum has also continued. No corrosion has ever 1 a de- tected. In one instance, 0.036-ineh diameter tantalum has broken in the aquarium after two years and three months on the caudal peduncle of a bass. The knotted end of Hie wire parted and the disk came off during a routine examination. Failures have also been noted in returns of 0.032- inch diameter wire after about one year on the caudal peduncles of wild bass. Tantalum still has promise, however, particularly if it can be incor- porated into a tag which is immobilized in some way. thereby eliminat- ing the working of the metal and permitting the tissues to grow to the wire. This is discussed more fully later. No adherence of tissue to the tantalum wire of Petersen tags occurred in aquarium experiments lasting several years. Movement of disks and wire as the fish swam apparently prevented it. Earlier conclusions about plastics have been confirmed. Cellulose ni- trate disks 0.045-inch thick are proving entirely satisfactory. Thick cel- lulose acetate disks (0.045-inch) used on wild striped bass are being re- turned in a generally satisfactory condition after Is months, although they are obviously not as good as nitrate. A disk' 0.030-inch thick wore down to 0.020 inch during two years on an aquarium bass, and another broke and dropped off. further confirming the inferiority of acetate. Position of Petersen Disk Tags Disk tags were tested on the caudal peduncle, under the first and sec- ond dorsals, and on the opercle. In general, except in the case of the opercle, the numbers of tests were too small and aquarium conditions were not rigorous enough to give very clear-cut results. The tests are nevertbeless of considerable interest and they will be summarized briefly, for valuable inferences can be drawn from them. In one experiment six disks on the caudal peduncle were compared with 11 under the dorsal fins, using 0.036 tantalum wire for all. Fish about 15 inches long were used. After two years and three months, when the fish all died, five of the six tags under the anterior end of the first dorsal were as good as new. The sixth had been lost earlier through crack- ing of a vinylite disk, which was found on the bottom of the tank. The five under the second dorsal were all still in place, although only one was in really good condition. There was a great deal of slack in the wires of two, and the remaining two had migrated upward a considerable distance and would soon have been shed. These results indicate that the first dorsal position is superior to the second. 212 CALIFORNIA FISH AXD GAME FIGURE 2. Location of Petersen disk tag on caudal peduncle of striped bass The six caudal peduncle tags were located as shown in Figure 2. Three were lost the first year : one through a cracked disk, and the others pos- sibly for the same reason or through the death of the fish, although this is uncertain. It was not until later that fish were tagged so they could be recognized individually without draining the tank, and the cause of some early losses is uncertain. Of the three still in place after two years and three months, the wire on one broke in handling, although the tag was otherwise satisf aetory ; and the other two had worked back about one-half inch and were quite loose. This broken tantalum wire was the same one mentioned earlier. In a companion experiment begun a month later with these same fish, 12 tags were placed under the first and second dorsal, using vinylite disks and stainless steel (Type 316, 0.036 inch diameter). One of the six under the first dorsal was lost early in the experiment, possibly through a cracked disk or the death of a fish. The other five were still on after two years and two months. Three were in satisfactory condition, but the other two had migrated up almost into the base of the fin and would soon have been shed. Four of the six under the second dorsal were still in place at the end of the experiment. One of those lost was observed about half way up through the fin after one year. At the next inspection, a month later, it had been shed. The second was shed after 18 months. Of the four remain- ing after two years and two months, two were satisfactory, one was very loose and one was at the very base of the fin and would soon have been shed. Here again there is at least an implication that the first dorsal location is superior to the second dorsal. A.QUAEIUW TESTS OP TAGS ON KTRII'KD BASS FIGURE 3. Diagrams of tags tested: (a) Petersen disk on opercle, (b) strap tag on opercle, (c) Atkins tag on opercle, (d) and (e) Atkins tags on back, (f) Oregon type tag and (g) staple rag 214 CALIFORNIA FISH AND GAME The performance of these dorsal tags with stainless steel wire was poor compared with the tantalum ones discussed earlier. This probably re- sulted partly from the difficulty of tying a good knot in the relatively thick (0.036 inch diameter) stainless steel, making a satisfactory appli- cation of the tag difficult to attain. There is little doubt that shedding of a similar sort will occur even more rapidly on wild fish. Unfortunately positions on the caudal peduncle were not available for this second experiment with stainless steel because old caudal tags from preceding experiments remained on so well. Six were still in a satis- factory state after more than three years. Another experiment was begun about one year after those just dis- cussed. The test fish ranged from about 10 to 20 inches in fork length. Thirteen Petersen disks were tested on the caudal peduncle. All disks were cellulose nitrate (diameter one-half inch, thickness 0.045) and all wires were 0.032 inch diameter. Soft-temper tantalum and the medium- soft and dead-soft temper type 302 stainless steels were used in about equal numbers with no apparent differences in behavior. Twelve of these caudal tags were still on and in a reasonably satisfactory condition after 14 months. Nine were on small bass initially 10 to 12 inches long, and the other four were on larger fish from 16 to 19 inches. Most of the tags appeared to have migrated backward about one-fourth inch during the 14 months, leaving well-healed scars to mark their passage. The thir- teenth tag had been shed after one year and two weeks. It was on a small fish 10 inches long. The wire had cut backward and upward until it worked out at the base of the upper caudal rays. Four disk tags under the first dorsal were included in this same test, using stainless steel wires. Two were in satisfactory condition after 14 months, another was very loose and the fourth was almost up into the dorsal fin itself. These were on medium-sized bass from 12 to 16 inches long. A large number of tags were placed on cheeks in this same experiment, us shown in Figure 3a, with most interesting results. Such tags have been used widely (Kounsefell and Kask, 1945). The rivets used on the cheeks of shad (Cable, 1950) proved infeasible because of the thinness of the opercular bones of bass. There was too much space between the rivet head which goes inside the cheek and the disk which goes on the outside. Worse, they did not permit any adjustment of this distance for large and small fish. The usual 0.032-inch wires were accordingly resorted to for these ti'sts. They were headed into pins to avoid a knot on the inside which might injure the gills. These tags were a great disappointment. Sizable holes were worn in the cheek rapidly, even in the case of large bass with thick opercular bones. ( >nly 8 of 19 tags remained on for 14 months, and all of these were in an unsal isfactory condition. One had made a hole large enough to pull i lie w bole tag through readily, and another had made one almost as large. The others had migrated down and back for considerable distances: a lid I inch in three cases, three-fourths inch in two cases, and one-half inch in two i-ases. Two fish died after about three months, and the tags had already worn large, irregular holes around the pins in the cheeks of both. The other nine opercular disk tags were shed: two after less than two months, one after six months, two after 10 months, and four after A.QUARIUM TESTS OP TAGS ON STRIPED l: \ 215 ;i lion I one year. The rate of shedding would undoubtedly have been even more rapid in wild lish. II is obvious thai opercles of striped bass undergo too much continual movemenl for this type of tag, which soon cuts its way through the hard, thin opercular bone. While rivets mighl bave been slightly better, be cause of their larger diameter, there is little doubl thai they would have behaved in a similar manner. The cutting of large holes in the cheek h;is also been reported iii experiments with Petersen tags on the opercles of ha, 1, lock ( Etounsefell, 1942). The caudal peduncle location for Petersen tags was adopted early Eor use on striped bass in the field because it appeared besl in early aquar- ium experiments, and because it was thoughl thai more growth would be possible and less entanglement in gill nets would occur than under the dorsal tins. Great care is exercised in field tagging to place the wire in the exact spot shown in Figure 2. where it is surrounded by bone.1 It was hoped that this would retard shedding. In the aquarium, tags in this position have commonly migrated back- ward at the rate of about one-four1 b inch per year, as already menl ioned. It is obvious that they will not stay on in the wild indefinitely, as had been hoped. However, indications are that they will be retained for at least a year on wild bass larger than about 12 inches. Their use is not recommended on smaller fish, however, for even in the aquarium they have tended to work out through the relatively tender tissues. Aquarium tests have clearly ruled out the opercle and the second dorsal of striped bass for Petersen disks, but some doubt remains about the first dorsal, which may prove equal or possibly superior to the caudal peduncle. The front end of the fish's body undergoes relatively little lateral motion during swimming, compared with the tail, and a tag under the first dorsal will be subject to less movement than one on the caudal peduncle. Moreover, the greater thickness of flesh through which tin1 wire passes will tend to retard migration through the tissues. Further experiments on wild fish will be required to resolve this point. STRAP TAGS This type of tag was commercially available only in monel metal, which has corroded so rapidly in previous experiments that it was obviously unsuitable. A fewT were therefore1 hand-fabricated from sheet stainless steel 0.020 inch thick. They were placed on the upper edge of the opercle, as shown in Figure 3b. < )nly one of five remained on after 14 months, and it had cut its way down the edge of the cheek a full inch, deforming it considerably in the process. This type of tag is clearly unsuitable for use on striped bass. Similar results have been reported for Pacific mackerel (Roedel, 1949). Strap tag's on the jaw, so commonly used for fresh-water fish, were not tried on striped bass because of the delicacy of their maxillaries and pre- maxillaries, and because such tags are believed to interfere too much with normal feeding. 1 The place is readily located externally. It lies halfway between the lateral line and the top of the caudal peduncle on a vertical line downward from the forward end of the little dorsal ridge in front of the caudal fin. 216 CALIFORNIA FISH AND GAME ATKINS TAGS A considerable assortment of Atkins tags was also tested. One type consisted of a small plastic blank, roughly one by one-fourth inch, sus- pended on a 0.015 tantalum wire. Ten of these were placed on the cheek as shown in Figure 3c. Eight were shed within three months, and the remaining two were gone within four. Without exception, the fine wire cut back rapidly through the bone. This same type of dangler behaved much better when the wire was looped through the back about three-fourths inch beneath a dorsal fin, as shown in Figure 3d. These held up surprisingly well, in view of the thin- ness and softness of the metal and the amount of movement they under- went. Perhaps the most significant result was the apparent adherence of the tissue of the fish to the tantalum wire in three of eight cases after 14 months, in spite of this considerable motion. The other five showed no such adherence. In all instances the wire on the side away from the dan- gler had become imbedded and was no longer visible. All of these tags remained on for 14 months, although one of them was on the point of breaking then, as a result of failure of the wire from continual working. The tag is not recommended for general use, because of the way it moves when the fish swims; preventing immobilization and leading to working of the metal. However, a modification (Figure. 3c) has recently been tried on wild catfish (Ictalurus catus), using 0.020 diameter tanta- lum wire, with promising results. Several other Atkins tags were less satisfactory. Small rectangles of stainless steel crimped onto heavy, braided nylon cord, diagrammed in Figure 3f, were obtained from the Oregon Fish Commission. Five were tried, but unfortunately four of the fish died too soon for an adequate test. The remaining one was on a bass about 20 inches long. The cord was threaded once through the back, well below the first dorsal. At all observations there were extensive raw areas on each side where the nylon entered. The cord worked its way out and was shed within about nine months, leaving a large, conspicuous scar. Shedding would probably have occurred even more quickly on a wild fish of the same size. Five similar tags fabricated from stainless steel blanks and Saran monofilament plastic were all shed within about two months, presumably because the steel cut the Saran. STAPLE TAG This tag, shown in Figure 3g, was developed to embody the desirable features of both the Petersen disk and the tantalum dangler, and to elim- inate the undesirable ones. The disk is largely immobilized by the two wires through the heavy muscle tissue of the back, which greatly reduce its freedom to move. Location well forward under the first dorsal where lateral movement of the fish's body is at a minimum may permit the tissues to adhere to the tantalum wire (0.020 inch diameter) and incor- porate it as a pari of the fish. Use of a single disk may also allow the other side to grow over completely, as happened with tantalum danglers on the back in the aquarium. It is also possible that elimination of one disk will permil much growth before the remaining one becomes completely im- bedded. Another apparent advantage is the reduced chance for entangle- ment of the tag iu gill nets, which is often such a serious problem. A.Q1 \i;ii H I l.s'l's OP TAG 0 i KIP! D »/ -I i Twenty tags of this type were placed on bass in the aquarium jusl one month before the fish were all lost. No changes of consequence occurred during the month. It will be some time before there will be an oppor tunity to tesl them again on striped bass. Thej are s promisin worth trying. Il musl I mphasized, however, thai thej are unproved, and some unanticipated disadvantage maj counterbalance the apparent advantages. 'This tag is much like the so-called "Archer" tap Rounsefell and Kask, 1945, p. 329). However, the latter was usually located on the dorsal or adipose fin, where rapid shedding is to be expected. A greal man} of the oilier tags described by Rounsefell and Kask were also in locations which inns! have led to early shedding. SUMMARY Knrther observations have confirmed the superiority of cellulose u it rate over cellulose acetate and vinylite for I 'etersen disk tags. Stainless steel tag wires (type 302. diameter 0.032 inches; type 316, diameter, 0.036) have never corroded or broken in salt-water aquarium test-. Tantalum wire (0.036 inch diameter) broke in one instance in the aqua- rium, after two years and three months on the caudal peduncle. There have been similar failures in returns from wild fish after about a year. Petersen disk tags were tested on the operde and caudal peduncle and under the first and second dorsals of striped bass. Those on the cheek were soon shed. The wire cut rapidly through the opercular hones, l n general, those under the second dorsal did not remain in place as well as thus,, under the first dorsal or on the caudal peduncle. There was some indica- tion that a location well forward under the anterior end of the first dorsal might be particularly advantageous. Tags on the caudal peduncle stayed on well, but migrated backward about one-quarter inch per year. Some of the dorsal tags also migrated badly, while others remained in place indef- initely. Further field tests will lie required to determine the relative merits of the first dorsal and caudal peduncle locations. Well applied tags of suitable materials will usually remain on in both places for several years in the aquarium. Strap tags and Atkins tags on the cheek were shed rapidly. Atkins ta L91. Calhoun, A. .1. 1950. California angling catch records from postal card surveys: L936-1948 ; with an evaluation of postal card nonresponse. ('alii'. Fish and (lame. vol. 36, no. 3, p. 177-234. 218 CALIFORNIA FISH AND GAME Calhoun, A. J., D. H. Fry, Jr., and E. P. Hughes 1951. Plastic deterioration and metal corrosion in Petersen disk fish tags. Calif. Fish and Game, vol. 37, no. 3, p. 301-314. Clark, G. H. 1934. Tagging of striped bass. Calif. Fish and Game, vol. 20, no. 1, p. 14-19. 1936. A second report on striped bass tagging. Calif. Fish and Game, vol. 22, no. 4. p. 272-283. Merriman, Daniel 1941. Studies on the striped bass (Roccus saxatilis) of the Atlantic Coast. U. S. Fish and Wildl. Serv., Fish. Bull., vol. 50, no. 35, p. 1-77. Roedel, P. M. 10411. Movements of Pacific mackerel as demonstrated by tag recoveries. Calif. Fish and Game, vol. 3."), no. 4, p. 281-291. Rounsefell, G. A. 1942. Field experiments in selecting the most efficient tag for use in haddock studies. Amer. Fish. Soc, Trans., vol. 71, p. 228-235. Rounsefell, G. A., and J. L. Kask 1945. How to mark fish. Amer. Fish. Soc, Trans., vol. 73, p. 320-363. THE EFFECT OF THE COMMERCIAL CANNING PROCESS UPON PUFFER POISON1 By BRUCE W. HALSTEAD and NORMAN C. BUNKER School of Tropical and Preventive Medicine College of Medical Evangelists, Loma Linda, California Although puffers, fishes belonging to the family Tetraodontidae, are generally classified as "trash fishes" they have I a used as food by native peoples for many centuries. Puffers are widely distributed through- ou1 most warm sens and the range of some species extends into temperate waters. These fishes are known by many vernacular names, viz., blow- fish, tambor, rabbitfish, swellfish, swellbelly, swelltoad, blower, jugfish (U. S.), toadfish, toado (Australia), blaser (Dutch Eas1 [ndies), [kan buntal (Malaya), tambores (Cuba'), botete (Philippines and Latin America), fugn (Japan), etc. In spite of their extensive use for food by native peoples, the roe and other viscera of the puffer are generally considered to be extremely toxic. The threatened depletion of some of our fisheries resources lias stim- ulated certain organizations to conduct research along lines which will contribute to an increased utilization of our marine resources. A number of fishing companies have been experimenting with the commercial possi- bilities of "trash fishes." According to Vudkin (1945), Sphoeroides maculatus (Bloch and Schneider), the common puffer of the Atlantic coast, began to appear in increasing numbers in the fish markets of northeastern United States about 194.'!. The market appearance of this fish was of some concern to those who were acquainted with the virulent properties of puffer roe. Toxicity studies on the roe of 8. maculatus have been conducted by Yudkin. lie found that the roe of the Atlantic puffer contains a poison whose pharmacological properties are similar to those of Japanese tetraodontoxin. Fortunately the toxin, which has a cardio-inhibitor action, is not present in sufficient quantities in 8. maculatus to be lethal to human beings. There are about 10 different species of tetraodons inhabiting the waters of western North and Middle America. Some of these species may be considered as candidates for the commercial fish markets of the Pacific Coast. At the present time there is only fragmentary data regard- ing the toxic properties of the puffers of the tropical Pacific. However, there is considerable information concerning the chemical and pharma- cological properties of tetraodontoxin from .Japanese puffers but the 1 This investigation was supported by a research grant from the National Institutes of Health, Public Health Service, and a contracl with the I >ffice of Naval Research, De- partment of the Navy (NONR-205(00) ). Submitted for publication September, 1952. (219) 220 CALIFORNIA FISH AND GAME bulk of this work is not readily available to most American researchers. Since it is a well-established fact that tetraodontoxin is not destroyed by ordinary cooking methods it was considered advisable to conduct a series of experiments relative to the effect of the commercial canning process upon the virulence of puffer poison. This is the first of a series of papers which are now in preparation relative to the problem of puffer poisoning. MEDICAL ASPECTS OF PUFFER POISONING The potential significance of puffer poisoning can be most readily appreciated by briefly reviewing the situation as it has existed in Japan. Pawlowsky (1927) states that during the period from 1888 to 1909 there were 3.106 known cases of puffer poisoning in Japan, which resulted in 2,090 deaths, an average of about 100 deaths a year. According to Fukuda and Tani (1937), there were 909 deaths resulting from fugu poisoning during the 10 year period from 1927 to 1937 which accounted for 44 percent of the total food poisonings in Japan. Fugu poisoning has been regarded as Japan's most important single cause of food intoxication. Recent reports from the Japanese National Ministry of Welfare and Health (in litt.) reveal that during 1949 to 1951 there were 389 re- ported cases with an over-all mortality rate of 57 percent. Puffer poisoning usually occurs as a result of ingesting the gonads, liver or intestines. The musculature of most Japanese species are said to be nontoxic (Tani, 1945) . But one is not safe in assuming that the flesh of all tropical species are innocuous. Recent tests in our laboratories on the musculature of Arothron hispidus (Linnaeus) and A. meleagris (Lacepede), common puffers of the central Pacific, indicate that the musculature of these species may at times be violently toxic. This pres- ent study will reveal that the musculature of certain Japanese puffer species may also be toxic on occasion. Japanese scientists have demonstrated that there is considerable fluc- tuation in the toxicity of oriental puffers. A similar situation has been found to occur in A. meleagris. Specimens taken in French Frigate Shoals, Hawaiian Islands, during January, 1950, proved to have nontoxic musculature while those taken at Hull, Phoenix Islands, during July, 1950, were violently toxic. The factors which influence toxicity fluctua- tion are not known at this time, but apparently there is some relationship to the gonadal activity of the fish. Tani (1945) has shown that the toxicity Level is highest during the spawning season of the year, which for most oriental species is during May and June. The gonads begin to enlarge about November and reach their maximum size and weight about Feb- ruary or March. The toxicity level reaches its peak a short time before the spawning season, continues for a few weeks after spawning and then gradually declines. The symptoms of intoxication generally develop rapidly and consist essentially of numbness and tingling of the lips, tongue and finger-tips, accompanied by dizziness, headache, weakness and dyspnea. Gastro- intestinal symptoms such as nausea, vomiting and abdominal pain are usually present. The i'orementioned symptoms may be accompanied or EFFECT OF CANNING i PON PI I l i i; POl 0 221 followed by additional neurological disturbances which in fatal ca may be very severe, viz., severe ataxia, impairment of speech, convulsions and muscular paralysis. Death results from respiratory paralysis and may occur in less than one hour or up to 20 24 hours, It death does nol occur within *_' I hours, the chances for the recovery of the patienl are considered to be g 1. Richardson i 1861 records two deaths which oc curred a1 the Cape of Good Elope as a resull of ingesting the liver of a puffer | Sp. iiiihl.. probably Arothron nigropunctatus Bloch and Schneider), or A. stt Hal its (Bloch and Schneider . One death occurred in 20 minutes and the other in 17 minutes. The t reatment of tetraodon poisoning is largely symptomal ic. There is no known antidote. Injections of epinephrine are believed to be of value (Kimura 1927). However, even with the besl medical care the over-all mortality rate is considered to be about 60 percent. CHEMICAL NATURE OF PUFFER TOXIN The chemical properties of puffer poison have been studied by a num- ber of Japanese workers. Taliara (1894, 1910), fshihara i 1924), Nagai and Ito (1939), Kanayama (1943), Yokoo (1948, 1950), Hashimoto and Migita (1951 ) and others, but probably the most complete work is that by Taliara. His work lias been well summarized by Vndkin (1944: 12-13 as follows: " Tetrodotoxin 2 exists as a white, hygroscopic powder, very readily soluble in water and insoluble in the ordinary organic solvents. It consists of carbon, hydrogen, oxygen and nitrogen; the provisional chemical formula is assigned as Ci6H31N( >,,-,. The substance does not give any of the protein reactions nor is it precipitated by the alkaloidal re- agents. The possibility that the poison is a protamine derivative is en- tirely excluded. The lethal dose with tetrodotoxin obtained by the new method (Tahara 1910) is 4 mg. per kgm. body weight. : Other than statements to the effect that tetrodotoxin is neither a protein, an alkaloid, nor a protamine, Taliara does not go into the chemical structure of the poison. " Nagai and Ito (1939) have suggested that the poison is probably an acyclic compound. Judging from an exhaust ive review of the scientific literature dealing with puffer poison, the exact chemical structure of tetraodontoxin and the source of the poison are still unknown. The reader is referred to the works of Tani (1945), Suehiro (1947), and Kimura (1927), for more complete reviews of the over-all problem. MATERIALS AND METHODS The puffers used in this study were obtained from the Central Whole- sale Fish Market at Kyobashi, Tokyo. Japan, by Dr. Tokiharu Abe. The specimens were captured along the coast of southern Japan and in the East China Sea during the winter and early spring of 1950-51. The fishes were iced soon after capture, later sharp-frozen and then shipped to our laboratory under refrigeration. The fish were not permitted to thaw until the extracts were prepared. -The designation tetrodotoxin (or tetrodowtoxin as it is sometimes spelled) is derived from the misspelling of the puffer .minis, Tetraodon. Taxonomists have relegated Tetrodon to synonymy but this misspelled term is still deeply entrenched in medical and biochemical literature. We are recommending that the correel spelling of the prefix be used, thus : tetraodontoxin and not tetrodotoxin (Halstead — in press). 222 CALIFORNIA FISH AND GAME FIGURE 1. (1] Sphoeroides rubripes chinensis Abe; (2) Sphoeroides vermicularis porphyreus (Temminck and Schlegel); (3) Sphoeroides vermicularis radiatus Abe; (4) Sphoeroides vermicu- laris vermicularis (Temminck and Schlegel). EFFECT OF CANNING I PON PU1 I BB PO] I --••' Taxonomic identifications were made with the use of Abe's (1949) critical analyses, "Taxonomic studies on the puffers (Tetraodontidae, Teleostei) from Japan and adjacent regions." The terminology as sug- gested by Abe have been adopted in this report. Tissue extracts were pre- pared from the following Japanese puffers Figure 1 Sphoeroides rubripes chinensis Abe. iSphucruidcs v< rmicuUiris porphyreus (Temminch and Schlegel). Sphoeroides vermicularis radiatus Abe. Sphoeroides vermicularis vermicularis (Temminck and Schlegel , All of the examples examined were ma1 are specimens, but in some in- stances sexual determination was questionable because some of the fishes were taken during a period of gonadal quiescence. Tissue extracts were prepared from the musculature, liver, intestines and gonads. Two ml. of distilled water were added dor each gram of flesh. The material was then homogenized in a Waring blendor. ["he homi enate was centrifuged at 2,000 r.p.m. for 25 minutes a1 aboul 1.000 "G's." One ml. of the supernatant fluid was injected intraperitoneally into four white laboratory mice of the California (aviary Strain No. 1, weighing 15 to 25 gm. each. In order to determine the effects of the proc- essing upon the virulence of the toxins, samples of each tissue specimen were tested both before and after canning. No mouse was used more than once. The canning process, which approximated commercial canning proce- dure, was conducted in the research laboratory of the Van (amp Sea Food Company at Terminal Island, California. The musculature, liver, gonads and intestines were placed in separate commercial one-half pound cans. In some instances cross sections were taken from the entire fish which included both musculature and viscera. For each can of flesh 3.5 gm. of ordinary table salt were added. The open cans were then placed in a steam exhaust at 100 degrees C. for 10 minutes. Water heated to 82.2 degrees C. was then added to fill the can. Lids were placed on the cans and sealed. The cans were next placed in a steam retort under a pressure of 12.5 pounds per square inch at 116.6 degrees C. for 75 minutes. The cans were cooled by immersing them in cold water upon their removal from the retort. All fish samples were processed in the same manner and at the same time. The fish were canned on July 3, 1952, and the cans were opened and tested on July 9th, 10th, 14th, 15th and 17th. There was no correlation observed between the length of time the fish remained in the can and their toxicity. Extracts were prepared immediately upon re- moval of the tissue samples from the can and were tested upon mice without further delay. •71944 224 CALIFORNIA FISH AND GAME RESULTS The results of the experiment appear in Table 1. TABLE 1 Results of Intraperitoneal Injections of Puffer Tissue Extracts Into Mice Death Time — min. sec. Species Tis- sue Mouse No. Ext. No. Tox- Tox- Before Canning icity liter Canning icity 580-1 S. r. chinensis M 1 30:20 S At, ixic, hypoactive3 W M 2 29:10 S i it W M 3 26:15 S C It W M 4 28:25 S t tl W 580-2 tt it L 1 01:55 S t it W L 2 01:30 S t tt w L 3 02:20 S I tt w L 4 01:50 s t tt w 580-3 u u Go* 1 21:50 s ' " w Gcf 2 29:55 s I It w GJ> 3 about 40 minutes s 1 It w Gc? 4 about 1 hr. 20 min. M I It w 580-4 tt tt I 1 03:50 S Asymptomatic N I 2 04:20 S it N I 3 05:35 s a N I 4 04:45 s it N 581-1 S. v. porphyreus M 1 02:35 S ' J asymptomatic N M 2 02:35 S " N M 3 02:15 s it N M 4 02:35 s " N 581-2 tt it L 1 01:20 s " N L 2 01:20 s " N L 3 01:30 S " N L 4 01 :30 s « N 556-1 S. v. radiatus M 1 27:30 S 1 Asymptomatic N M 2 26:25 s " N M 3 25:30 s " N M 4 26:05 s a N 556-2 It it L 1 09:05 s a N L 2 13:05 s tt N- L 3 15:20 s a N L 4 16:00 s a N 557-1 tt tt M 1 05:45 s tt N M 2 05:30 s a N M 3 05:00 s a N M 4 05:00 s tt N 557-2 It 11 L 1 01:20 s 07:303 s L 2 01:30 s 16:50 S L 3 01:30 s 08:20 s L 4 01:30 s 11:35 S 557-3 II It G9 1 00:50 s 10:20 s G9 2 00:50 s 10:15 S G9 3 00:40 s 07:35 s G9 4 00:45 s 08:40 s 557 I It It I 1 02:25 S l Asymptomatic N I 2 02:00 s a N I 3 02:30 s it N I 4 02:30 s it N EFFECT OF CANNING i PON PI il 1.1; POl ON TABLE 1 Continued Ext. \u. Tis- Mouse No. 1 li i III It) Spei b u e 1 Ml. 1 ,-,.M ! S, . rmieul ■ M I i \ 551 2 u 1. i I N .-,;,! :: It tt 1 ! I I u \ 552 1 n tt M I 33:30 a ■I N M 2 J:00 \l 3 27:45 s N M I 34 tl N 552 2 tt tt 1, I 03: Hi a II X L 2 03:10 N 1. :: 03:40 a II N 1. 4 03:55 a H 560-1 it tt M 1 29:40 a W M 2 i ictive, survived \\ tl W M 3 27 a t. it \V M 4 s II II \v 560-2 u it L 1 05:10 a u L 2 03:11) s il \v L, 3 04:50 8 u L 4 03:45 S .t w 560-3 tt it G 9 1 01:10 > tl \v G 9 2 01:0.5 s .. w G 9 3 01:25 8 II w G9 4 01:05 S " w 562-1 tt it M 1 28:00 s Vsj tic X M 2 18:25 a •• X M 3 17:50 3 ii N M 4 29:25 S .i X 562-2 tt tt L 1 06:45 8 .. X L 2 06:50 s •• X L 3 07:30 S .. X L 4 08:00 s .. X Legend for Table I: M = muscle; L = liver; G = gonads; I = intestine. 8 Juice in can positive but I sample negative. N = negative: mouse continues to remain asymptomatic during the maximum 36 hours. W = weakly positive: mouse shows definite symptoms such as lacrimation, diarrhea, ruffling of the hair, hypoactivity, etc., but the animal recovers. M = moderately positive: mouse develops ataxia, I activity, and/or paralysis and dies within a period of 1 to 36 hours. S = strongly positive: mouse ilrvelops ataxia, which is usually followed by clonic or tetanic convulsions of varying degrees, paradoxical respiration, respiratory paralysis and death occurs within a few seconds to one hour. The results appearing in Table 1 seem to indicate that the virulence (based on mouse death time) or toxin concentration and heat lability varies with the species, individual specimen and the organ from which the toxin vas obtained. As previously mentioned. Tani (1945) and otl have demonstrated that the toxin concentration with the hotly of the tish varies also with the season of the year. There is also evidence to indicate that a puffer species may be poisonous in one locality ami not in another. Tissue extracts prepared from the liver, gonads and intestines of Sphocroides rubripes chinensis, S. v. vermicularis and S. vermicularis radiatus were found to be strongly toxic prior to canning but only those samples taken from the liver and gonads of S. v. radiatus continued to remain so after canning. However, even in this latter instance it will he noted that the virulence of the toxins were somewhat attenuated as indi- cated by the increased length of time required to kill the mice. The toxins of S. r. chinensis and S. v. vermicularis are considerably more heat labile than that of 8. v. radiatus. In both S. r. chinensis and 8. v. radiatus the intestinal toxins which were found to be strongly positive prior to can- ning were rendered innocuous by the heating process. If the food-chain 226 CALIFORNIA FISH AND GAME theory is correct, then the chemical properties of puffer toxin are prob- ably modified by the organ system through which the toxin passes. The four fish specimens of 8. v. vermicularis which were tested proved to be quite variable. Only one fish was found to yield weakly positive re- sults after the canning process. Extracts No. 551-1, 2, 3 were used as controls. One specimen of 8. v. porphyreus was tested and the toxin was found to be heat labile. In analyzing the contents of the can after processing, it was found that the toxin was limited to the liquid fraction. None of the muscle samples were found to be toxic after canning, since tetraodontoxin is water soluble. Tani (1945) states that "unless one eats a large amount of puffer flesh, a person cannot become intoxicated from eating the musculature of the puffers of Japan, Korea and China. ' ' The results obtained in this study reveal that the musculature of the four Japanese puffers under consid- eration may on occasion be strongly toxic. In the case of 8. v. porphyreus the virulence of the toxin obtained from the musculature was found to approximate that obtained from the liver. SUMMARY 1. The threatened depletion of some of our marine resources has stim- ulated a number of organizations to investigate the commercial possi- bilities of various trash fishes. Since puffers, which are generally con- sidered to be trash fishes, have recently been introduced on the Bast Coast as food fishes and may be sold on the West Coast, attention is called to the potential public health significance of these fishes. 2. The most severe forms of puffer intoxication generally occur as the result of ingesting the liver, intestines or gonads. However, the musculature may frequently be violently toxic. Fugu, or puffer poisoning, is accompanied by severe neurological symptoms which may result in the death of the victim by respiratory paralysis. The over-all mortality rate is said to be about 60 percent. There is no known specific antidote for tetraodontoxin. 3. The toxin is not a protein, an alkaloid nor a protamine. Some workers believe it to be an acyclic compound. The provisional formula has been assigned by Tahara, a Japanese investigator, as Ci6H3iNOi6 but the exact chemical structure of the toxin is unknown. 4. Tissue extracts were- prepared from samples of the musculature, liver, gonads and intestines of four common Japanese puffers, Sphoer- oides rubripes chinensis Abe, and 8. vermicularis porphyreus (Tem- minck and Schlegel). Samples of the same specimen were tested both before and after the canning process in order to determine the heat lability of the toxin. The virulence of the extracts obtained from the muscle, liver and gonads of some of the specimens of 8. r. chinensis and 8. v. vermicularis was markedly attenuated but not completely destroyed. Extracts from the liver and gonads of 8. v . radiatus were only slightly icted by the heating process and continued to be strongly positive. In the case of 8. v. porphyreus and certain specimens of 8. v. chinensis, 8. v. radiatus and 8. v. vermicularis the toxins were found to be heat labile. Apparently the property of heat lability is subject to a wide EFFECT OF CANNING i PON PI PFEH POl I '-- < degree of fluctuation. The Factors contributing to tins, situation are uol clearly understood a1 this t ime. 5. In general, the problem of poisonous fishes will become of increasing public health significance as attempts are made to develop the Bhore fisheries of I he t ropical Pacific. ACKNOWLEDGMENT The authors are grateful to Dr. Tokiharu A.be, the Office of Naval Research and the Xaval Supply Depot, Departmenl of the Navy, Yo suka, Japan, for aid in the procuremenl and shipping of the puffers used ill this study. We are indebted to Mr. < iilberl ( '. Van ( lamp and I >r. S. Lassen of the Van Camp Sea, Kood Company, Terminal Island, for use of their canning facilities. Appreciation is expressed to the Translating Unit, National Institutes of Health. Public Health Service, and the Research Division of the Abbott Laboratories, North Chicago, for providing us with translations of the Japanese publications. The -Japanese scientific publications were obtained as a resull of the cooperative efforts of Drs. Y. Hiyama, T. Abe, I. Tani, N. Kawamoto, M. Migita, V. Bishimoto, Medical Department, ( lommander Naval For of the Par East, Public Health and Welfare Division, Headquarters of the Par East Command and the National Ministry of Welfare and Health of the -Japanese Government. REFERENCES Abe, T. 1949. Taxonomic studies on the puffers (Tetraodontidae, Tclcostei) from Japan and adjacent regions — V. Synopsis of the puffers from Japan and adjacent regions. Biogeogr. Soc. Japan, Bull., pt. 1, vol. 14. no. 1. p. L-15. 1949. Ibid., pt. 2, vol. 14, no. 13, p. 89-140, 2 pis. Fukuda, T.. and Tani, I. 1937. Statistische Beobachtung iiber die Fugu vergiftung. Japanese Jour. Med. Sci., 4 Pharm., vol. 10, p. 48-50. Halstead, B. W. In Some general considerations of the problem of poisonous fishes and ichthyo Press sareotoxism. Copeia. Hashimoto, Y., and Migita, M. 1951. On a method of quantitative analysis for Eugu (puffer) toxin. Japanese Soc. Sci. Fish., Bull., vol. 1G, no. 8, p. 341-346. Ishihara, F. 1918. tiber die physiologischen wirkungen des fugutoxins. Mitt. Univ. Tokyo Med. Fak., vol. 20, p. 375-426, 3 pis. 1924. Studies iiber das fugutoxin. Arch. Exper. Path. u. Pharmakal., vol. L03, p. 209-218. Kanayama, S. 1943. Purification of puffer poison and its chemical characteristics. Fukuaka Med. Mag., vol. 36, no. 4, p. 395-401, 1 fig. Kimura, S. 1927. Zur Kenntnis der Wirkung des tetrodongiftes. Tohoku .lour. Exp. .Med.. vol. 9, p. 41-05, 7 rigs., 7 tabs. Nagai. J., and Ito, T. 1939. On the chemical study of fugu (Sphoeroides) poison. Jour. Biochem., vol. 30, no. 2, p. 235-238, 2 tabs. 4—71944 228 CALIFORNIA FISH AND GAME Pawlowsky, E. N. 1927. Gifttiere unci ihre Giftigkeit. Jena, Verlag Yon Gustav Fischer, p. 412-421. 3 figs. Richardson. J. 1861. On the poisonous effect of a small portion of the liver of a Diodon inhab- iting- the seas of southern Africa. Jour. Linn. Soc, vol. 5, p. 213-216. Suehiro, Y. 1!>47. Practice of fish physiology. Tokyo, Takeuchi Bookstore, ISO p., 28 figs. Tahara, Y. 1894. Report of the discovery of puffer poison. Zeitschr. d. japan pharniaz. Gesellsch., vol. 14, p. ? (Not available to authors). 1910. tlber das Tetrodon-Gift. Biochem. Zeitschr., vol. 30, p. 255-275. (Not avail- able to authors.) Tani. I. 1945. Toxicological studies on Japanese puffers. Imperial Chem. Corp. (Japan), vol. 2, no. 3, p. 1-103, 22 figs. Yokoo, K. 1948. Chemical study on tetrodotoxin. Rept. no. 1. Inst. Phvs. and Chem. (Japan) vol. 24, no. 3, p. 136-139. 194S. Chemical study on tetrodotoxin. Rept. no. 2. Jour. Med. Hiroshima, vol. 1, no. 2, p. 52-53. 1950. Chemical studies on tetrodotoxin. Report no. 3. Isolation of Spheroidine. Japanese Chem. Jour., vol. 71, no. 11, p. 590-592. Yudkin. W. H. 1944. Tetrodon poisoning. Bingham Oceanogr. Coll. Bull. vol. 9, art. 1, p. 1-17, 1 fig- 1945. The occurrence of a cardio-inhibitor in the ovaries of the puffer, Sphoeroides maculatus. Jour. Cell, and Comp. Physiol., vol. 25, no. 2, p. 85-95, 3 figs. A PRELIMINARY REPORT OF THE TOXICITY OF THE GULF PUFFER, SPHOEROIDES ANNULArUS* By DON R. GOE Zoology Department, University of Southern California, Los Angeles, California and BRUCE W. HALSTEAD School of Tropical and Preventive Medicine College of Medical Evangelists, Loma Linda, California Since "trash fishes are receiving an increasing amounl of attention as potential protein food sources, it was considered advisable to conduct a series of studies relative to the public health significance of poisonous puffers. The work reported in this paper was done preliminary to an extensive investigation of the physiological activity of various tissue extracts from the gulf puffer, Splioci-oirfrs annulatus (Jenyns). The physiological studies which are now in progress will he reported at a later date. ( )nly the results dealing with the toxicity experiments will he given at this time. These show that the gulf puffer should not he con- sidered for use (whole, parts, or cleaned.) for either human or animal consumption. The earliest record of poisonous fishes from the Gulf of California is that of Calvijero (1706). In his history of Baja California he mentions the incident of four soldiers who were poisoned by eating the liver of a botete, or puffer, which was captured in the Gulf of California. One of the soldiers died in 30 minutes; another died a short time later; a third, who had chewed, the liver without swallowing it. lost consciousness until the following day; the fourth, "who had barely touched it." was sick for several days. This incident is also mentioned by Pellegrin (1899) and Phisalix (1922), who state that the liver and musculature of the botete were commonly used by the natives of Baja California for poisoning stray dogs — a custom which is still practiced in some regions today. These authors state that the puffer eaten was T< trodon heraldi I riinther, which is listed by Jordan, Evermann and Clark (1930") as a synonym of S. annu- latus (Jenyns). Aside from the forementioned references we have been unable to locate any literature relative to the pharmacological properties of the toxin of the gulf puffer. MATERIALS AND METHODS Ninety-six specimens of Sphoeroides annulatus I Figure 1 I were col- lected by the senior author and Robert Smith by underwater spearing and hook-and-line from Bocochibampo Bay about three miles north of Guaymas, Sonora, Mexico, during June 23-25, 1952. 8. annulatus ranees 1 This investigation was supported by a research grant awarded to the School of Tropica] and Preventive Medicine by the National Institutes of Health, Public Health Service, and a contract with the Office of Naval Research Department of the Xavv tXOXK- 205(00)). Submitted for publication September, 1952. (229 ) 230 CALIFORNIA FISH AND GAME FIGURE 1. The gulf puffer, Sphoeroides annulaius (Jenyns). (from Hiyama) from San Diego, California, to Mazatlan, Mexico. This species is particu- larly common along sandy shores and bays throughout the Gulf of Cali- fornia. The fish were quick-frozen within a few minutes after capture and remained frozen for two to three weeks until the extracts were prepared. Twelve specimens were selected at random from the lot. The weights of the whole fish, liver, and gonads were taken prior to preparation of the tissue extracts. The material was homogenized in a Waring blendor to which two ml. of distilled water were added for each gram of tissue. The homogenate was centrifuged and one ml. of the supernatant fluid injected intraperitoneally into a male white laboratory mouse, of the California Caviarjr Strain No. 1, weighing 17 to 27 gm. (average 20.9 gm.). Four mice were used in testing each extract. Their reactions were observed and recorded. The cessation of all breathing movements was taken as the time of death. The weights and injection results appear in Table 1. A summary of the averages of weights and death times appears in Table 2. RESULTS AND DISCUSSION Of the 12 fish tested, none were found to possess toxic muscle, 11 speci- mens had strongly toxic livers, and four had strongly toxic gonads. If the average death times after injection of liver extract are compared with the weights of the whole livers as percentage of body weight (Table 1), there seems to be no correlation between organ size and toxicity (death time) . The average death time for liver extract was 3 minutes and 10 sec- onds (range 1 :20-14 :45). Although the data are limited, there is appar- ently no correlation between gonad size and toxicity. The average death time for gonadal extracts was 13 minutes and 8 seconds (range 2 :50- 40:45). The toxic reaction herein referred to consisted of the following symp- toms : an initial hyperkinesia followed by a mild ataxia ; as the ataxia progressed, dyspnea set in, developed into apnea and death ensued ac- companied by moderate to severe clonic convulsions. The heart continued to beat for several minutes after the cessation of breathing. The mecha- nism of the action of this toxin is being investigated and will be reported at a later date. In checking over some of our earlier records it was found that one specimen of this species had been collected on April 4, 1951, from San Felipe, Baja California. The fish was handled and extracts prepared in a manner similar to that employed with the Guaymas specimens. Extracts were made of the musculature, liver and intestines. The gonads were too small for testing purposes. The tissue samples weighed about 7 gm. each. TOXICITY OF THE Gl U PUFF! R TABLE I 231 * — Asymptomatic. t Toxic reaction. TABLE 2 Summary of Averages Fish No. \\ eighl <>f Bsh (gm.) Tissue \\ ■ Lght of Bam pie Peroent of bod i 1 1 i in 0.31 1 nisi- death time 'min tion 1 137 mus. liv. gon. 1 1 13 IS .' 1 :, 1 on — — 2 477 mils. liv. gon. 12 2 1 I..". t 3 : 155 IIIUS. liv. gon. 13 15 0.5 ii I I I I". t 4 339 IIIUS. liv. gon. 16 13.5 28 :; 38 8.25 1 :. : 1 1 t 5 .. 387 mus. liv. gon. 13 19 1 4.90 0.25 t 6 . 291 mus. liv. gon. 10 15.5 1.1'.". :, 32 0.43 3:00 20:18 + t 7 290 mus. liv. gon. 11 4.5 1.25 1.55 0.43 1 :30 31 :30 t 8 307 mus. liv. gon. 10 13.25 1 4.31 0.33 i 19 t 9 275 mus. liv. gon. 10 11.5 3.25 4.18 1.18 3:00 4:26 t t 10 254 mus. liv. gon. 7 6.5 1 2.55 0.39 J 1 1 t 11 248 mus. liv. gon. 10 12 6.5 4.83 2.62 2:52 t 12... 676 mus. liv. gon. 11 26 53.25 3.84 7.87 2:15 t Item Average Range Number of items Fish weight . - . . . Liver " Gonad " Muscle " Mouse " Liver death time . 353.0 gm. 14.22 gm. 9.7 gm. 11.16 gm. 20.9 gm. 3 :10 min. 13 :08 min. 248-676 gm. 1. 5-26.0 gm. 0. 5—53 .76 gm. 7.0-13.0 gm. 17.0-27.0 gm. 1 :20-14 :45 min. 2 :50-40 :4."> min. 12 12 12 12 144 44 (11 fish) Gonad death time 14 t 4 Bsh) 232 CALIFORNIA FISH AND GAME Four mice were used in testing each extract. The average death times were as follows (min : sec) : muscle— 26:21 (range: 17:15-30:00) liver— 14:31 (range: 8:54-17:30) intestines — negative, mice remained asymptomatic. It will be noted that in the case of the Guaymas specimens, the mus- culature was found to be nontoxic, while that of the San Felipe specimen gave a strongly positive reaction. Thus, it can be seen that the toxicity of the same organs of the puffer are subject to considerable variation. Whether this fluctuation is on a seasonal, regional, or merely anatomical basis has not been determined thus far. The problem of toxicity fluctua- tion in puffers has been discussed in detail elsewhere (Halstead and Bunker 1953). Studies are now in progress which should shed additional light on the matter. SUMMARY The toxicity of extracts obtained from the muscle, liver, and gonads of 12 specimens of the gulf puffer Sphoeroides annulatus ( Jenyns) collected near Guaymas, Sonora, Mexico, is reported. Also included are data from one specimen of this species collected from San Felipe, Baja California. Of the 12 fish from Guaymas, 11 had strongly toxic livers and four speci- mens had strongly toxic gonads. None of the muscle extracts from the Guaymas specimens proved to be toxic. However, the muscle extract as well as that of the liver from the San Felipe specimen was strongly toxic. The extract from the intestine of the San Felipe fish was negative. Appar- ently the toxicity level of the gulf puffer S. annulatus is subject to con- siderable fluctuation. Exactly what the factors are which control toxin production is not known at this time. The high incidence of toxicity in the livers over that of the other organs may have some significance since the liver is generally considered to be the principal organ for detoxification in the body. This present study was conducted preliminary to a more extensive investiga- tion concerning the origin and physiological actions of the toxin from 8. annulatus. The results of this study reveal that the musculature and viscera of the gulf puffer, S. annulatus (Jenyns), are frequently toxic, hence should not be considered for human consumption. LITERA1URE CITED Clavijero, F. J. 1706. The history of (Lower) California (Translated from the Italian and edited by Sara E. Lake and A. A. Gray). Stanford Univ. Press, Book II, p. 213-14. Halstead, B. W.. and X. C. Bunker lit.",:;. The effecl of the commercial canning: process upon puffer poison. Calif. Fish and Game, vol. 39, no. 2, p. 219-228. Jordan, D. S.. B. W. Everman and H. W. Clark 1930. Check list of the fishes and fishlike vertebrates of North and Middle America north of the northern boundary of Venezuela and Colombia. U. S. Comm. Fish., rept. for 1928, pt. 2. p. 499. Pellegrin, J. L899. Les poissons vfinfineux. Paris, These, p. 45-47. Phisalix, M, 1922. Animaux venimeux et venins. Paris, Masson & Cie, vol. 1, p. 590. OBSERVATIONS ON THE EFFECT OF BLACK POWDER EXPLOSIONS ON FISH LIFE' By DONALD H. FRY, JR., and KEITH W. COX Marine Fisheries Branch, California Department of Fish and Gam-- This article describes a field tesl used to verify the recommendations of Ilubbs and Rechnitzer in their paper "Reporl on Observations I' signed to Determine Effed of Underwater Explosions on Fish Life." The effect of explosions on fish was made very prominenl off the Cali- fornia coasl by the desire of various oil companies to make geophysical explorations of the formations beneath the waters adjacenl to the Cali- fornia coast. The method firsl used involved the use of submarine explo- sions of dynamite to prod nee a shock wave which would travel downward through the earth and be reflected from various underlying rock strata. By plotting the depth of these strata at many different points, it was possible to map the subsurface geology and pick out the spots a1 which oil was most likely to be discovered. California law math1 it necessary for the oil companies to obtain per- mits from the Fish and (lame Commission before firing explosives under- water. To summarize a lon;iy. California. The first, on June 8, 1952, was marked by ;i registration of 308 fishermen and a total catch of 108 sharks and rays 1,800 po Is . The second, held eiuht weeks later on .July 27. resulted in a registration of 322 fishermen and a total catch of 106 sharks and rays 1.111 pounds . Sponsorship of the June s . Their use of an "X" in the San Francisco column of their table indicated that they must have had a specimen from that locality, although their next speci- men was from Santa Barbara, and there was none from the area between the two localities. Otherwise the northernmost recorded specimen was found on the beach immediately north of Pt. Conception by Dr. Carl I.. Hubbs (1916). Other rarities included two male specimens of the round stingray ( I'robatis halleri). The first. 372 mm. and 1 ,";., pounds, was taken June 8 (CAS 20587), and the second, 405 mm., 1 .';, pounds, was taken July 27 (CAS 20620). From Mr. Follett's studies, the northernmost record for this species is again credited to Dr. llubbs (1920). He observed a speci- men on the sandspit at the mouth of the estero at Goleta just north id' Santa Barbara. The latter site is the type locality for the species. Thus the range of the round stingray is extended an approximate 170 air-line miles, or about 200 coastline miles northward from Goleta to Elkhorn Slough, Monterey Bay. 1 Submitted for publication November, 1952. ( j::t ) 238 CALIFORNIA FISH AND GAME One of the smallest sharks taken at the July derby (280 mm. male) was found after laboratory examination to be a gray smoothhound (Mustelus californicus) . This is the first known specimen of this species taken in the slough. Despite the fact that the type locality for the gray smoothhound is San Francisco, where it is not now known to occur, its northernmost range for the present will have to rest on this immature specimen (CAS 20619). The largest fish of the June derby was a female bat ray of approxi- mately 100 pounds ; this is a slight increase in size over the 85-pound prize-winning specimen of the previous year. For the July derby the largest fish was again a female bat ray but this time the weight was much less, i.e., 56 pounds. Two tails projecting from the cloaca of this female suggested the possibility of obtaining newborn rays for the aquarium. TABLE 1 Comparison of Catches Made at the Elkhorn Slough Shark Derbies Number cau| ?ht Percentage caught May, 1951 June, 1952 July, 1952 May, 1951 June, 1952 July, 1952 Leopard shark Triakis semifasciata Males - 7 7 15 17 9 7 23 29.5 47.5 26.6 13.9 54.5 .925 .925 Females. . ... . ..... Total ...... . . . :.. Shovelnose guitarfish Rhinobatos productus Males .. .... 14 4 14 32 3 12 16 18 31 15.1 Females. ... ______ _.. Total . _ 18 8 21 15 27 32 49 1 21 18 46.2 Gray smoothhound Mustelus californicus Males .. _ _ .94 Bat ray Holorhinus californicus Males .. . ._ Females. . .. Total.. .. ... ... . 29 59 1 1 39 1 36.8 Thornback Platyrhinoidis triseriata Females Round stingray Urobatis halleri Males .944 Females Total catch 61 237 108 1,800 308 105 1,100 322 Total weight in lbs Number registered fishermen THE [Q52 SI1 VRK i»l 1:1:1 1 ■j:;: i Dissection revealed two small females each with pectoral tin> neatly Folded over the bach and lying in the uterus with the posterior pari of the bodies directed towards the cloacal opening (Figure 1 , Had tin- Shark Derby not intervened, they would probablj have been born within the next few hours but unfortunately they were nol alive al the time of removal from I he pa renl . 'Idiese unborn rays were 502 and 510 mm. in length I 185 mm. from tip of snout to posterior edge of pelvic fins for both I and weighed I'M and Mil grams, respectively (('AS 2062] I. In both of these specimens the natal sear was still apparent. Most obvious were the extremely Long tails. Measurements revealed that the tail Length of these, and other very young specimens, was 53 to 63 percent of the total Length, whereas older specimens are usually in the 30 to L5 percenl range. It is possible that further data will reveal that young ba1 stingrays lose some of the tip portion of the tail during the first Few weeks of Life. These unborn bat rays were apparently fairly good sized for a small female caught several days later in San Francisco Bay (natal scar not visible) measured only 435 mm. (161 mm. to posterior edge of pelvic fins) and weighed 250.7 grams (CAS 20622). A male bat ray CAS 20624) caught at the Coyote Point Shark Derby on September 1 I. meas- ured 400 mm. (151 mm. to posterior edge of pelvic tins and weighed FIGURE 1. Unborn bat stingrays removed from the uterus of the prize-winning 56-pound female at the July, 1952, Elkhorn Slough Shark Derby. See text for discussion of change in the relative lengths of the tails. Photograph by Kenneth Innes. 240 CALIFORNIA FISH AND GAME 187.3 grams. That this size is approximately that of newborn rays in San Francisco Bay is indicated by fonr individuals born at about the same time at the diving bell at Fleishacker Beach. These four specimens were transferred to tanks at Steinhart Aquarium where they seemed to do well on a diet of fish pellets. We had them for about a month but unfortunately lost all of them within one week due to an unknown air- bubble disease affecting the internal organs. Gudger (1951) has recently published a very interesting paper on ' ' How difficult parturition in certain viviparous sharks and rays is over- come. ' ' Although he is of the opinion that all rays have tail presentation of young at birth, he was able to find only a few records substantiating this important detail. Suffice to say that California's bat ray agrees with what is known of other rays in having tail presentation at birth. At the 1951 derby there was an indication of an atypical sex ratio among the bat rays with the catch of 29 specimens being composed of 8 males and 21 females. In the 1952 derbies the ratio was more normal. However, the ratio for shovelnose guitarfish was quite abnormal for both years : for 1951, 4 males and 14 females ; and for 1952, 3 males and 12 females ; and 18 males and 31 females. Fluctuation in the guitarfish catch has been marked, although for the first two derbies the numbers caught were about the same, i.e., 18 and 15 specimens, respectively. However, for the third derby the catch of this species was nearly tripled with a total of 49 specimens. Thus, for the three derbies the shovelnose guitarfish were 29, 14 and 46 percent of the total catch. This fluctuation should not be wholly unexpected since guitarfish schools are known to move in and out of shallow bays at irreg- ular intervals. This movement is also true of leopard sharks and such might account for the 16 specimens taken at the July derby as compared with the catch of 32 taken one month earlier at the June derby. Little is known of the movements of bat rays. The writer suspects that this species has a more static population than does any of the sharks. If such were the case, then the drop in catch from 59 to 39 from the June to the July derby might be partially clue to the mortality that occurred at the June derby. Catch records for the 1951 derby have previously been published by Herald and Dempster (1951). THE COYOTE POINT DERBY The Sixth Animal Coyote Point Shark Derby was held on Sunday, September 14, 1952, with the fishing limited to South San Francisco Bay between the hours of 7 a.m. and 3 p.m. Sponsorship was again by the San Mateo Lions Club and the Coyote Point Yacht Club. The total catch of 1871 sharks and bat rays (6,620 lbs.) was the largest recorded for any of the derbies. The 1,484 registered fishermen were 139 fewer than the number that participated in last year's derby. The details of the catch are presented in Table 2, together with a comparison with previous years. The data for the 1951 derby has not been reported although the earlier data appears in Herald and Ripley (1951). THE [952 SHARK DERBI1 TABLE 2 Comparison of Catches Made at the Coyote Point Shark Derbies Brown smool bhound Rhinotriacia henlei I leopard shark Triakis s< mifasciat > 1 logfish Squalus acanlhias Soupfin Galeorhinus lyopterus. Sevengill cow shark Notorynchus maculatum - Six'gil] COW shark //( xanchus griseus Thresher Alopias mlpinus Bat ray Holorhinus calif ornicus- Total catch Total weight in lbs Number registered fishermen. \n inluT caughl June, 1948 :,l .",7 12 129 *9S2 Sept., 1950 539 261 (ill 59 89 1,015 4,216 *1,406 Sept., 19.-. I 712 312 99 26 168 61 1,378 6,550 *1,623 Si 1 'i . 1952 Pcrci ■ii'li 1 June, 1948 798 190 2.3 .'lid 301 59 1,871 6,620 *1,484 II x 11.2 '.1 :; 4.7 1951 51 7 25 . 7 .:. 7.2 1 .9 - 12 2 .01 11 .(11 11 8.8 1 I 12 e 26.2 1 2 [0.7 Hi. 1 0 0 3.2 * The number of registered fishermen may not he too significant since many persons buy tickets in order to help the derby's objectives (chilil aid and child care) or to he eligible for the drawing for the prizes. The largest shark captured at the 1952 derby was again a sevengilJ —an 84-pound female which upon dissection was found to be sexually immature. The stomach contained the large head of what had apparently been a striped bass of some 20 pounds. This was the third Largesl sevengill known from the bay. The largest, a 177-pound specimen, was caughl by Don Hunter off Brisbane during 1941. The second largest weighed 106.1 pounds and was taken during the Fish and Game San Francisco shark survey of 1943. At the other shark derbies the largesl sharks (sevengills ) weighed 34, 20, Til and 64 pounds respectively. The increase in number of sevengills has been pronounced ( 168 specimens o{' the 1950 derby representing 5.8 percent of the total catch, as compared with the 301 specimens of the 1952 derby representing 16 percent of the total catch). One of the strangesl specimens of the 1952 derby was what was ap- parently an albino sevengill (Figure 2). This specimen, now cataloged as CAS 2062:!, did not have the pink eyes usually considered the marK of the true albino. The iris was unpigmented and the pupil dark blue. whereas the reverse was the case in other preserved sevengills. i.e., the 242 CALIFORNIA FISH AND GAME FIGURE 2. An albino sevengill shark (870 mm.) caught at the 1952 Coyote Point Shark Derby — photographed alongside another specimen with normal pigmentation. Both were preserved at the time the photograph was taken. Photograph by Kenneth Innes. iris dark-colored and the pupil white. Whether this is a case of pseudo- albinism due to a glandular deficiency, or true albinism due to heredity, remains to be determined. The second surprise of the derby was the tremendous increase in the number of soupfin. Although these sharks were not eligible for prize awards since it is illegal to catch them in the bay, nevertheless there were 200 of them (10.7 percent of total catch) brought to the judge's stand. The writer was able to find only one fisherman who had recognized the soupfin while fishing and he had thrown back about 18 individuals (not recorded in Table 2) . Thus the lack of a commercial soupfin fishery seems to be having a beneficial effect on the species — provided that the Coyote Point Shark Derby catches are any true indication. Another strange specimen should be mentioned. One of the 490 leopard sharks had a heavy rubber band around its gill area (Figure 3). Sharks and other fishes with bands around parts of their bodies have not been unknown in the past but this is apparently the first in California. The shark probably picked up the band while nosing over the bottom in search of food, and this undoubtedly occurred when the shark was much sinall'M-. However, the possibility is not to he ruled out that the band was placed on the shark by some pseudo humorist when it wras caught — and then subsequently released. Dr. Gudger has reported sev- eral cases — a mackerel with a rubber band through the center of its body (1928) ; a 15-foot mackerel shark with an automobile tire around its midriff (1931) ; haddock, dogfish, halfbeaks and mackerel with rubber bands (1937) ; and fishes with iron rings about the body (1938). Data on these derbies were taken by Kenneth Innes, Walter Schneebeli, Norval Green, Robert Dempster, Leonard Goodman, Robert Van Bozarth and the writer. THE [O52 11 MM-, in ki-.il- w FIGURE 3. From the Coyote Point Shark Derby, a 30-inch leopard shark with a heavy rubber band around the gill region. There was no indication of wearing on the undersurface of the body, although there was considerable erosion on dorsal surface. Photograph by Kenneth Innes. LITERATURE CITED Gudger, E. \V. 1928. A mackerel (Scomber scomirus) with a rubber band rove through its body. Amer. Mus. Novitates, no. 310, 6 p., •"• Bgs. T.i.'iT. Fishes and rings: Notes and illustrations of various fishes wearing rubber bands. Sci. Mon., vol. 4">. p. 503 512, 7 figs. 1938. The fish in the iron mask and other fishes with iron rings around their necks. [bid., vol. 46, p. 281-285, 7 figs. 1951. How difficult parturition in certain viviparous sharks and rays is overcome. Jour. Elisha Mitchell Sci. Soc, vol. t',7. no. 1. p. 56-85, Is- ii--. Gudger, E. W., and W. H. Hoffmann 1931. A shark encircled with a rubber automobile tire. Sci. Mon., vol. •"■•"■. p. 275- 277, 1 photo. Herald. Karl S.. and Robert P. Dempster 1952. The 1951 shark derby at Elkhorn Slough, California. Calif. Fish ami Game, vol. 38, no. 1. p. 133134. Herald, Earl S., and Wm. Ellis Ripley 1951. Tin' relative abundance of sharks and bal stingrays in San Francisco Bay. Ibid., vol. ::7. no. ::. p. 315-329, •". figs., '< tabs. Hubbs, Carl L. 1916. Notes on the distribution of three California rays. Copeia, no. :;7. p. ^.. 1920. Notes on the rays of California, [bid., no. 86, p. 82. Jordan, David S., and Charles H. Gilbert 1881. List of the fishes of the Pacific <'oast of the United States, with a table showing the distribution of the species. TJ. S. Nat. Mus., Proc. vol. .".. p. 452-458. NEW FISHWAYS ON THE YUBA AND FEATHER RIVERS' By J. A. APLIN Marine Fisheries Branch, California Department of Fish and Gan As pari of a Long term program for the betterment of fishing in Cali- fornia, the Department of Fish and Game has been investing in basic stream improvement. Money for this work has been made available bj the allocation of funds from the tax on pari-mutuel horse race betting. The program of wildlife restoration is supervised by the Wildlife Con- servation Hoard. Three Large fish Ladders have been completed as pari of this work. Two of the new fishways are at Daguerre Point dam on the Yuba River about It) miles up the river from Marysville. Above the dam there are lf> miles of gravel beds suitable for salmon spawning, since the dam was built, there have been xevy few salmon nests found in this upstream area in marked contrast to the stream bed below the dam where many salmon nests are found each year. This is in spile of the fad that the upstream channel is more desirable as a breeding area because it eon- tains water throughout the year. There was an old Ladder a1 the south end of the dam (Figure 1) made by building concrete walls across a narrow channel in the rock with the upper portion built of planking. This wooden portion was destroyed by high water several years ago. The 700-foot length of this dam made a ladder at each end necessary it' the tish were to get over before becoming exhausted. Also an island uear the middle of the dam separates the downstream channel for 150 yards. It is quite unlikely that a fish reaching the dam on one side of this island would ever £et to a ladder on the other side. Making any structure stand that is exposed to the river at this loca- tion is difficult because of the small rocks and sand which are carried by the water at high (lows. The abrading action of this gravel makes heavy construction imperative. The new ladder at the south end of the dam was started in September, 1950. To reach the site, construction equip- ment had to be brought across the top of the dam and unusually high water early in the fall slowed completion of the job. However, the proj- ect was finished early enough in 1 95] to be used by the runs of anad- romous fish arriving later in the spring. At one time five kinds of migrating fish were seen in this ladder. As well as the expected king salmon and steelhead, there were shad, striped bass ami squawfish. Submitted for publication September, 10.">2. (245) FIGURE 1. Remains of the old ladder at the south end of the Daguerre Point dam, Yuba River. Photograph by D. H. Fry, Jr. The fishway on the north end of the dam is shown in Figure 3. Al- though the high water carried away the concrete forms at the project just as they were ready to have cement poured into them, construction was completed during the summer of 1951 in time for the fall run. Here salmon and steelhead were seen in the ladder at the same time. \i;\v FISHWAYS JIT FIGURE 2. The new ladder at the south end of the Daguerre Point dam The combined cost of the two Daguerre Point fishways was $65,000. It is expected that the increased area now made available to spawning will add to the runs of salmon and steelhead ascending the Yuba River in the future. The largest of the three new fishways is on the Sutter Butte dam in the Feather River. It is located about 10 miles downstream from Oroville and about five miles northeast of Gridley. There has been a fishway on this dam but it has proved definitely unsatisfactory. Several reasons contribute to its lack of effectiveness. As this old fish ladder is not ac- cessible from either bank of the river except at very low water, no adjust- ment of the flow through it can be made. Also, the dam is several hundred feet long which makes it difficult for fish to find the entrance. This factor is aggravated by the position of the entrance about 20 feet downstream from the face of the dam. During some years when a heavy flow in the river occurs, at the time of the upstream migration of salmon, the fish pass over the dam without much trouble. However, this is the exception and cannot be depended upon. 248 CALIFORNIA FISH AND GAME FIGURE 3. Fishway at the north end of the Daguerre Point dam. Photograph by J. A. Aplin, July, 1952. \I.\V KISHWAY8 I1' FIGURE 4. The new fishway at Sutter Butte dam on the Feather River. Phofograph fay J. A. Aplin, July, 1952. Work on the new fishway was begun in October of 1950. Construc- tion was difficult, as the river bed at this location is composed of Large cobbles to a considerable depth. These shifting rocks made the building of a cofferdam around the foundation area slow and the up- welling of water from below hard to stop. Exceptionally high water within a month after work was started destroyed the cofferdam and washed away a number of the concrete forms. Work had to be abandoned until the lowering of the water in The summer of 1951. On October 24, 1951, a flow of water was started through the fishway. although work was still going on, and within a few minutes upstream migrating salmon were seen entering it. Within an hour several dozen fish had passed through the ladder and others were coming in an almost continuous procession. This was particularly encouraging as the tisli had to jump over a temporary wall which had only six inches of water flowing over it. This wall was removed a few days later and access into the fishway was much easier. The project was officially completed on November 8, 1951, at a cost of $45,000. OFFICIAL COMMON NAMES OF CERTAIN MARINE FISHES OF CALIFORNIA' By PHIL M. ROEDEL Marine Fisheries Branch, California Department of Fish and Game PURPOSE OF OFFICIAL NAMES The fundamental reason for the State's assigning official names to its marine fishes is to assisl m the collection of accurate catch statistics. For the Department of Pish and Game to understand the State's many fisheries it is essentia] thai the catch, both sport and commercial, of each species be known. A consistent terminology on the pari of both the industry and sportsmen is of vital importance in the collection of accurate records, for confusion and inaccuracy will result it' ;i given species is listed by different names in different parts of the State and if a certain name can mean any of several species. LEGISLATION The importance of uniform terminology was recognized yens ago by the State Legislature. According to Walford (1931, p. 5) a law enacted in 1919 provided that "The Fish and (lame Commission shall have the power to decide what is the common usage name of any variety. ' ' In 1933, the law was changed to its present form. Article 5 (Commercial Pishing Reports), Section 1093, of the Fish and Game Code provides that : "The names used in the receipt for designating the species of fish dealt with must be those in common usage, and may be designated by the commission." "While this law applies specifically only to commercial landings, and consequently, to species entering the commercial catch, it has been the policy of the department to assign common names to other than com- mercial varieties, both fresh water and salt, to insure uniformity in State publications and records and to attempt to attain uniformity in com- mon usage on the part of all fishermen. PRIOR LISTS The first comprehensive list of official names appeared in Fish Bulletin Xo. 28 (Walford, 1931). This list covered the more important fresh-water fishes as well as the leading marine bony fishes, sharks and rays. A few vears later sharks and rays were treated more fully in Fish Bulletin Xo. 45 (Walford. 1935). By the late l!>40's, stocks of both of these bulletins were exhausted and in new publications it seemed wise to change several 1 Submitted for publication December, 1952. (251) 252 CALIFORNIA FISH AND GAME of the authorized names — some because they were coined and were not accepted by the public, others because they proved a detriment in market- ing. The revised official list of marine bony fishes appeared in Fish Bul- letin No. 68 (Roedel, 1948) and the reasons for the changes made were set forth by Roedel (1949). Fish Bulletin No. 75 (Roedel and Ripley, 1950) contained accounts of all species of sharks and rays known from the State and to each an official name was assigned. All fresh-water species of the State were assigned names by Shapovalov and Dill (1950) . PRINCIPLES GOVERNING OFFICIAL LISTS Stability is of prime importance if a list of official names is to serve its purpose. Once established, a name should never be changed unless there are substantial reasons for it. While changing the name of an unimpor- tant variety not segregated as a species by the fisherman would have little or no effect on the record system, any change affecting a major variety could have a serious effect. However, "official" names are patently worthless if they are not used. Errors will occur in the selection of names and common usage will change. Particularly, attempts to apply "logical" vernaculars in the face of established ' ' inappropriate ' ' names are usually doomed to failure. Further, it has happened that common usage names lacking in "sales appeal" have been assigned to species then of no sig- nificance only to have them emerge as commercial varieties but handi- capped on the market by unappetizing vernaculars. A certain latitude must be allowed to care for these situations. Several rules have governed the selection of official names, all subject to the guiding principle that the purpose of the names is to assist in the compilation of accurate records. Ideally, a name should be in sole use throughout a species ' range and would not be applied to any other North American species. Unfortu- nately, relatively few names have such universal and sole application. It then becomes necessary to evaluate snch names as are applied to a species with regard for the points which follow : 1. Usage in California by both commercial and sport fishermen and the fishing industry. 2. Usage in other areas, particularly adjacent states. 3. Usage on other official lists. 4. The name should not have undesirable connotations which might impair marketability. 5. The name should be brief and descriptive. 6. The name should indicate rather than confuse relationships. In practice in recent years, points one and four have carried the most weight. Other lists, particularly that of the American Fisheries Society ' 194*1. have been given I'ull consideration. Eowever, usage on the Pa- cific Coast, particularly in California, prevents our adopting all accepted names on these lists. The departures express the consensus of California workers and it is hoped that future committees on common names will give due consideration to Pacific Coast terminology. Point six has been given the least consideration. This is an unfortunate circumstance, but it is nonetheless true that some of our most firmly established vernaculars in in tAL COMMON \ \ \i i 253 are completely misleading. However, it would be futile to attempl their overt fctrow. In those cases where ;i species is no1 recognized as such by fishermen but is simply included in 8 broad category, such as "smelt, " it is possible to make ;i more "logical" selection. However, since tin- species is nol segregated by fishermen, giving it a name is largely an academic matter. The name will probably never gel beyond the bounds of the literature unless (as has happened I the species suddenly becomes of economic im- portance for itself and no1 as pari of a general category. Because of this chance, point four should never be overlooked in selecting names for obscure forms. Changes seem inevitable no matter how carefully initial selections may have been made. In general they have been made for one or more ol the following reasons : 1. To adopt established vernacular names or, lacking them, more appropriate names in those cases where the original official names me1 with no popular favor or proved inappropriate or misleading ; e.g., "ling- cod" for "Pacific cultus." 2. To adopt names desired by the industry for marketing purposes; e.g., "jack mackerel" for "horse mackerel. " 3. To make the names for species seldom caughl by or no1 separated in the catch by California fishermen conform with names used by other agencies and/or in other areas; e.g., "C-0 turbot " for " mutt led turbot.' THE PRESENT LIST This list includes some species not included in previous lists. None are of major significance in the State's fisheries but all appear sufficiently often to make official appellations seem wise. A few Mexican species not recorded from California waters are included as well because they are taken by California vessels or are of importance in California markets. These are marked with a dagger (t). In general, names have been given only to species likely to be caught by sport and commercial fishermen either by design or by accident. How- ever, all sharks and rays known from the State are included because names had been given them by Roedel and Ripley I 1950 t. All changes, other than minor emendations in orthography and addi- tions of optional attributives, are discussed at the appropriate place in the list. (Reasons for changes made from the lists of Walford, 1931 and 1935, and discussed by Roedel. 1949, are not restated, i A feature new to the official list is the sanctioning of a few alternative names, where two vernaculars are applied to the same fish in California and either name will lead to ready identification of the species in question. The preferred name is given primary listing. Another departure from previous lists lies in the use of optional attribu- tives. These will be found enclosed in parenthesis which indicate that another species with the same vernacular is found outside of the State's boundaries. Such attributives need not be used unless their omission might, in any given report or record, result in confusion with a species found elsewhere. 254 CALIFORNIA FISH AND GAME An asterisk denotes a name not previously listed. The names represent the consensus of departmental staff members. While it cannot be expected, in view of past experience, that this list will be immutable, we do hope that it more nearly approaches general acceptance. Our thanks, for their cooperation, go to Dr. C. L. Hubbs, Scripps Institution of Oceanography, La Jolla, Mr. W. I. Follett, California Academy of Sciences, San Francisco, and Mr. Raymond Cannon, Holly- wood, all of whom have given much thought to the vexing problems of vernaculars in connection with their own projected publications and with whom we have reached substantial agreement. >.- ■ COLLECTIVE TRADE NAMES In compiling catch records, a number of species are often grouped under one name, even though each species may have its own official name. This may be because the species are so alike in general appearance that little or no effort is made to separate them in the markets, because little reliance can be placed on the market identification or because only part of the total catch can be assigned accurately to the several species. The species composition is, in most cases, evident; for example, "sand- dab" might include any of the three species known from the State. How- ever, some trade names are deceptive and may include members of two or more families. These names include : 1. Eel. Includes moray (Gymnothorox mordax), monkeyf ace-eel (Cetidichthys violaceus) and rock-eel (Xiphister mucosus) . 2. Hardhead. Includes two fresh-water species, greaser blackfish (Orthodon microlepidotus) and hardhead (Mylopharodon conoce- phalus). 3. Kingfish. Includes queenfish (Seriphus politus) and white croaker (Genyonemus lineatus) 4. Perch. Includes all surfperches (family Embiotocidae), black- smith (Chromis punctipinnis) , half moon (Medialuna calif ornien- sis), opaleye (Girella nigricans) and sargo ( Anisotremus david- soni). 5. Rock bass. Includes the three members of genus Paralabrax (kelp, sand and spotted basses) . 6. Smelt. Includes various silversides (family Atherinidae) and various smelts (family Osmeridae). 7. Whitebait. Includes smelts (family Osmeridae) and may include the young of other fishes. COMMON AND SCIENTIFIC NAMES FAMILY HETERODONTIDAE— Horn Sharks (California) horn shark Heterodontus francisci (Girard) FAMILY CHLAMYDOSELACHIDAE— Frill Sharks Frill shark Chlamydoselachus anguineum Garman FAMILY HEXANCHIDAE— Cowsharks Sixgill cowshark Hexanchus griseum (Bonnaterre) Sevengill cowshark Notorynchus maculatum Ayres "Cowshark" adopted in place of "shark" as an aid in defining relationship. 0] in l \l. « <>\i HON NAM] 255 FAMILY ALOPIIDAE i i,i. bei (Common) thresher Hoping vulpinus (Bonnuterre) FAMILI LAMN [DAE Mackerel Shark Sail shark Lamna ditropis Hubb & Folletl Formerlj "mackerel shark." Salmon Bhark is the true vernacular In the Pacific Northwest. The species is relatively uncommon in California and d ool have a local name. Further, "mackerel shark" is applied l>.\ the American Fl to an Atlantic species. Bonito shark Tsurus glauous (MiillerA Henle) Man-eater —Carcharodon carchariat (Linnaeus) Formerly "greal white shark." "Man eater" is a widespread name and certain!) has the advantage of brevity and force. Rare in California. FAMILY CETORHINIDAE— Basking Sharks Basking shark Cetorhinus mawvmus (< runner i FAMILY SCYLIOKIIIMDAi: Cat sharks Filetail catshark Parmaturus waniurua (Gilbert i Brown catshark Vpristurua brunneua (Gilbert i "Catshark" adopted in place of "shark" as an aid in defining relationship. (California) swell shark Cephaloscy Ilium uter (Jordan & Gilbert) FAMILY TRIAKIDAE— Smoothhounds Leopard shark Triakis semifascUitu Girard Brown smoothhound Rhinotriacis henlei Gill Gray smoothhound Mustelus californicus Gill Sicklefin smoothhound Mustelus lunulatus Jordan & Gilbert FAMILY CARCHARHINIDAE— Requiem Sharks Tiger shark Galeocerdo cuvieri (Peron & LeSueur) Soupfin Galeorhinus zyopterus Jordan «.V: ( ■ illicit Blue shark Prionace glauca I Linnaeus I Formerly "great blue shark." The initial adjective was misleading. Bay shark Carcharhinus lamiella (Jordan & Gilberl i Roundnose shark Carcharhinus azureus (Gilberl & Starks) Listed by Roedel and Ripley (1950) as "gambuso" utilizing a Mexican vernacular. The new name is deemed more appropriate for use iu the United States. This spr, is very rare in California. (Pacific) sharpnose shark Scoliodon longurio (Jordan iV: Gilberl i FAMILY SPHYRNIDAE— Hammerheads Common hammerhead * Sphyrna zygaena (Linnaeus) Scalloped hammerhead* Sphyrna lewini (Griffith) Bonnethead Sphyrna tiburo (Linnaeus) FAMILY SQUALIDAE— Dogfishes Dogfish Squalus aoanthias Linnaeus Bramble shark Echinorhinus brucus ( Bonnaterre > (Pacific) sleeper shark Somniosus pacificus Bigelow & Schroeder FAMILY SQUATINIDAE— Angel Sharks (California) angel shark Squatina califomica Ayres FAMILY RHINOBATIDAE— Guitarfishes Shovelnose guitarfish Ehinooatos product us i Ayres) Mottled guitarfish Zapteryx exasperata (Jordan & Gilbert) FAMILY PLATYRHINIDAE— Thornbacks (California) thornback Platyrhinoidis triseriata (Jordan & Gilbert) * Species previously not listed. 256 CALIFORNIA FISH AND GAME FAMILY RAJIDAE— Skates California skate Raja inomata Jordan & Gilbert Big skate Raja binoculata Girard Longnose skate Raja rhina Jordan & Gilbert Starry skate Raja steUulata Jordan & Gilbert Rougktail skate Raja trachura Gilbert Sandpaper skate Raja kincaidi Garman Formerly "black skate," inappropriate in that the color is not at all black. The skin is actually the color and texture of sandpaper. FAMILY DASYATIDAE— Stingrays Round stingray Urobatis halleri (Cooper) Diamond stingray Dasyatis dipterurus (Jordan & Gilbert) (California) butterfly ray Gymnura mar mo rata (Cooper) Formerly "butterfly stingray." The sting is either small or absent and hence "sting- ray" was considered misleading. FAMILY MYLIOBATIDAE— Eagle Rays Bat ray Holorhinus calif ornicus (Gill) Formerly "bat stingray." This name does not have particular usage while "bat ray" is heard rather frequently. FAMILY MOBULIDAE— Mantas ("Pacific) mobula Mobula lucasana Beebe & Tee-Van (Pacific) manta Manta hamiltoni (Newman) FAMILY TORPEDINIDAE— Electric Rays (California) electric ray Torpedo califomica Ayres FAMILY CHIMAERIDAE— Chimaeras Ratfish Hydrolagus colliei (Lay & Bennett) FAMILY ACIPENSERIDAE— Sturgeons "White sturgeon Acipenser transmontanus Richardson Green sturgeon Acipenser medirostris Ayres FAMILY ELOPIDAE— Tenpounders (Pacific) tenpounder % Elops affinis Regan FAMILY ALBULIDAE— Bonefishes Bonefish Albula vulpes (Linnaeus) FAMILY DUSSCMIERIIDAE— Round Herrings (Pacific) round herring Etrumeus acuminatum Gilbert FAMILY CLUPEIDAE— Herrings Pacific herring Clupea pallasi Valenciennes (Pacific) sardine Sardinops caeridea (Girard) (American) shad Alosa sapidissima (Wilson) (Pacific) thread herring * Opisthonema libertate (Gunther) FAMILY EXGRAU LID AE— Anchovies Northern anchovy Engraulis mordax Girard Ocean northern anchovy E. m. mordax Girard Bay northern anchovy E. m. nanus Girard Deepbody anchovy Anchoa compressa (Girard) Slough anchovy Anchoa delicatissitna (Girard) Anchoveta * Cetengraulis mysticetus (Gunther) * Species previously not listed. t Gulf of California species known in California only from the Salton Sea. i IFFICIAL < <>\l MON NAM1 'l'u \\\\\\.\ OSMERIDAE Smell Whitebait Bmell : llloamerua elongatua (Ayr* I Eulachon Thaleichthy pacificua (Richard on) The name "cnndlefish" has considerable general usage and if heard almosl exclusivelj along thai portion of the California coasl where the pecie occur I' in sanctioned as 8 ii alternative name. Nighl smell ':: Spirinohua starksi (Pi k) Sacramento smell Spirinchus thaleichthya (Ay re I Surf smell Hypomesua pretioaua (Girard) Freshwater smell Hypomeaua olidua (Pallas) FAMILY SALMONIDAE Tr s Pink salmon Oncorhynohua gorbuacha (Walbaum) Chum salmon Oncorhynohua keta (Walbaum) Kin};' salmon Oncorhynohua tshawytacha (Walbaum) "Chinook salmon" is sanctioned ;is an alternative name. Though "king" has hereto fore been the onlj name accepted bj California, "chii k" is widelj used in the State mihI dominates in Oregon and Washington. In Alaska, i" the contrary, "king" i> used \ iri ually exclusivelj . Silver salmon Oncorhynohua kisutch (Walbaum) Sockeye salmon Oncorhynohua nerka (Walbaum) This salmon is of uo economic importance in California. We have previously used the name '"red salmon," but the consensus in the Pacific Northwest appears to favor "sockeye." Coasl cutthroal trout__ Salmo clarki clarki Richardson Steelhead rainbow troul Salmo gairdneri gairdneri Richardson FAMILY SCOMBERESOCIDAE Sauries (Pacific) saury Cololubis xairn (Lrevoort) FAMILY BELONIDAE— Needlefishes (California) needlefish Strongylura exilia (Girard) FAMILY EXOCOETIDAE Flyingfishes California flyingfish Cypselurus cdlifornicua (Cooper) .Mexican flyingfish* Oypselurua sp. FAMILY SYNODIDAE— Lizanllislies (California) lizardfish * Synodus luciocepa (Ayres) FAMILY ALEPISAURIDAE— Lancetfishes (Pacific) Iancetfish * Alepisaurus borealis Gill FAMILY MURAENIDAE— Morays (California) moray Gymnothorax mordax (Ayres) FAMILY CYPRINODONTIDAE- Killifishes (California) killifish . __Fundulus parvipinnia Girard FAMILY MERLUCCIIDAE— Hakes (Pacific) hake Merlucciua productus (Ayres) FAMILY GADIDAE Cods (Pacific) tomcod Microgadua proximua (Girard) (Pacific) cod Gadus macrocephalus Tilesius FAMILY LAMPRIDAE Opahs Opah * .Lampria regiua (Bonnaterre) FAMILY TRACHIPTERIDAE— Ribbonfisb.es (California) ribbonfish * Trachipterua rexsalmonorum .Ionian k\; Gilbert * Species previously not listed. 258 CALIFORNIA FISH AND GAME FAMILY BOTHIDAE— Lefteyed Flounders Bigmouth sole Hippoglossina stomata Eigenmann & Eigenmarm California halibut Paralichthys calif ornicus (Ayres) Fantail sole Xystreurys liolepis Jordan & Gilbert Pacific sanddab * Citharichtkys sordidus (Girard) Longfin sanddab * Citharichtkys xanthostigma Gilbert Speckled sanddab * Citharichthys stigmaeus Jordan & Gilbert The three species of sanddab were formerly listed under the collective term "sanddab." FAMILY PLEURONECTIDAE— Righteyed Flounders Arrowtooth halibut Atheresthes stomias (Jordan & Gilbert) Formerly "arrowtooth sole." It is not at present a marketed variety and does not have a vernacular in California save "turbot." The new name agrees with the American Fisheries Society list. Pacific halibut Hippoglossus stenolepis Schmidt Slender sole Lyopsetta exilis (Jordan & Gilbert) Petrale sole Eopsetta jordani (Lockington) Sand sole Psettichthys melanostictus Girard Diamond turbot Hypsopsetta guttulata (Girard) Curlfin turbot Plenronichthys decnrrens Jordan & Gilbert Hornyhead turbot Plenronichthys verticalis Jordan & Gilbert Formerly "sharpridge turbot." This fish does not have a vernacular other than "turbot." The new attributive is considered more appropriate and agrees with the American Fisheries Society (which, however, lists it as "hornyhead flounder"). C-0 turbot Plenronichthys coenosus Girard Spotted turbot . Plenronichthys ritteri Starks & Morris Scaly-fin sole Isopsetta isolepis (Lockington) English sole Parophrys vetulus Girard Rock sole Lepidopsetta bilineata (Ayres) Changed from "broadfin sole" to conform more closely with common usage. The new attributive is that used by the American Fisheries Society. Dover sole Microstomias pacificus (Lockington) Deepsea sole * Emoassichthys bathybius (Gilbert) Rex sole Glyptocephalus zachirus Lockington Starry flounder Platichthys stellatus (Pallas) FAMILY CYNOGLOSSIDAE— Tonguefishes (California) tonguefish Symphurus atricauda (Jordan & Gilbert) FAMILY SERRANIDAE— Basses Cabrilla f Epinephelus analogus Gill Striped bass Roccus saxatilis (Walbaum) (California) black sea bass Stereolepis gigas Ayres Broomtail grouper * Mycteroperca xenarchus Jordan Gulf grouper* Mycteroperca jordani (Jenkins & Evermann) Kelp bass Paralabrax clathratus (Girard) Sand bass Paralabrax nebulifer (Girard) Spotted bass 1 Paralabrax maculatofasciatus (Stein- dachner) Formerly "spotted sand bass." Changed in the interests of simplicity and to conform with such usage as exists. FAMILY ATHERINIDAE— Silversides (California) grunion Leuresthes tenuis (Ayres) Jacksmelt Z- Atherinopsis calif or niensis Girard Topsmelt Atherinops affinis (Ayres) Bay topsmelt A. a. littoralis Hubbs San Francisco topsmelt A. a. affinis (Ayres) Kelp topsmelt A. a. cedroscensis Hubbs Island topsmelt L. a. insularum Gilbert * Species previously not listed, t Not recorded from California. OFFICIAL < <>\i \io\ N \ M I FAMILY MUGILIDAE Mullel (Striped) mullet Uugil cephalns Linnaeus FAMIL1 SPHYRAENIDAE Barracuda (California) barracuda Sphyraena argentea Qirard FAMILY CARANGIDAE Jacka (California) yellowtail Seriola dorsalis (Gill) Pilot tisli * Naucratea ductoi (Linnaeu (Pacific) jack mackerel Trachurua aymmetricua (Ay re I (Mexican) scad Decapterua hypodua Gill FAMILY STROMATEIDAE Butterfishea (California) pompano Palometa 8imillima (Ayr< I FAMILY CORYPHAK\II>AK I )«.lphinfish( (Common) dolphinfish * Coryphaena hippurua Linnaeus FAMILY ECHENEIDAE— Remoraa (Common) remora * Retnora remora i Linnaeu FAMILY SCOMBRIDAE— Mackerela Pacific mackerel PneumatophorM diego (Ayres) FAMILY CYBIIDAE— Spanish Mackerels "Wahoo f Acanthocybium solandri (Cm ier I Sierra t Scomberomoru8 aierra Jordan & Star! Earlier reports of this species from California are now believed to refer to the Mon- terey Spanish mackerel. (Monterey) Spanish mackerel* Scomberomorua <-oncol<»- (Locking ton) California honito Sarda lineolata (Girard) Mexican bonito f Sarda velox Meek & Hildebrand FAMILY KATSUWONIDAE— Skipjacks Skipjack Ratauwonua pelamis (Linnaeus) Black skipjack* Euthynnua lineatua Kishinouye Bullet mackerel * Auxis sp. FAMILY THUNNIDAE— Tunas (California) bluefin tuna Thunnua saliens Jordan & Evermann Formerly regarded as identical with the Atlantic '/'. thynnua. Recenl studies (Godsil and Holmberg, 19")0) showed differences between Atlantic and Pacific specimens which, in the opinion of Dr. C. L. Hubbs and Mr. W. I. Follett, warranl recognition of the California bluefin as a distinct form, provisionally as a distinct species. (Pacific) albacore Thunnua germo (Lacepede) (Pacific) yellowfin tuna Neothunnua macropterua (Temminck >.V: Schlegel I Bigeye tuna t Parathunnua aibi (Temminck & Schleg FAMILY TRICHIURIDAE— Cutlassfishes (Pacific) cutlassfish * Trichiurua nitena Garman FAMILY ISTIOPHORIDAE— Sailfishes (Striped) marlin Uakaira mitaukurii (Jordan & Snyder) FAMILY XIPHIIDAE— Swordfishes Swordfish Xiphiaa gladiua Linnaeus Because this is the only species known, the old name of "broadbill swordfish" was felt unduly long. It is called either "broadbill" or "swordfish" but. at least in Cali- fornia, not "broadbill swordfish." Use of "broadbill" alone is sanctioned as an alternative name. * Species previously not listed. t Not recorded from California. 5—71944 260 CALIFORNIA FISH AND GAME FAMILY XENICHTHYIDAE— Salemas (California) salema Xenistius calif or nien sis (Steindachner) The coined name "bigeye bass" has been applied to this fish but is not appropriate because the fish is not a bass. Tuna fishermen who use this species and its Galapagos relatives as bait refer to them as "salema." The fish has no vernacular in California. FAMILY HAEMULIDAE— Grunts (California) sargo Anisotremus davidsoni (Steindachner) FAMILY SCIAENIDAE— Croakers Black croaker Cheilotrema satumum (Girard) Spotfin croaker Roncador stearnsi (Steindachner) White croaker Genyonemus lineatus (Ayres) Formerly "kingfish," which is henceforth sanctioned as an alternative name because of its use in the Monterey area. In Southern California where the fish is most abundant, it is generally called "tomcod" or "tommy," and "tomcod" or ''tomcod croaker" would be the name most closely approaching common usage. However, "tomcod" is reserved for Microgadus proximus and hence is not available. "Kingfish" is generally felt to be most inappropriate for this small and relatively undesirable species despite its local usage at Monterey. "White croaker," a coined name, seems reasonably appropriate and worth an effort to popularize. Yellowfin croaker Umbrina roncador Jordan & Gilbert (California) corbina Menticirrhus undulatus (Girard) Queenfish Seriphus politus Ayres White seabass Cynoscion nobilis (Ayres) Shortfin corvina Cynoscion parvipinnis Ayres This Mexican fish, which now rarely if ever reaches California waters, has been listed as "shortfin sea bass." It, like the three species following, is caught in quan- tity in the Gulf of California by both Mexican and American fishermen. There the universal vernacular for all four is "corvina." Gulf corvina *f Cynoscion othonopterus Jordan & Gilbert Orangemouth corvina *% Cynoscion xanthulus Jordan & Gilbert Striped corvina *| Cynoscion reticulatus (Giinther) Totuava t Cynoscion macdonaldi Gilbert FAMILY BRANCHIOSTEGIDAE— Blanquillos Ocean whitefish Caulolatilus princeps (Jenyns) FAMILY EMBIOTOCIDAE— Surfperches Heretofore each species has been termed simply "perch" preceded by the appropriate attributive. The typical surf dwellers are now identified by the name "surfperch," those associated with the ocean but not primarily with the surf are "seaperch," Avhile those of varying habitat remain "perch." Barred surfperch Amphistichus argenteus Agassiz Redtail surfperch Amphistichus rhodoterus (Agassiz) Calico surfperch * Amphistichus koelzi (Hubbs) Walleye surfperch Hyperprosopon argcnteum Gibbons Silver surfperch* Hyperprosopon ellipticum (Gibbons) Spotfin surfperch * Hyperprosopon anale Agassiz Rainbow seaperch Hypsurus caryi (Agassiz) White seaperch . Phanerodon furcatus Girard Sharpnose seaperch * Phanerodon atripes (Jordan & Gilbert) Rubberlip perch Rhacochilus toxotes Agassiz Pile perch Rhacochilus vacca (Girard) Black perch Embiotoca jacksoni Agassiz Striped seaperch Embiotoca lateralis Agassiz Pink seaperch Zalembius rosaceus (Jordan & Gilbert) Shiner perch Cymatogaster aggregata Gibbons Island perch * Cymatogaster gracilis Tarp Kelp perch Brachyistius frenatus Gill Reef perch * Micrometrus aurora (Jordan & Gilbert) Dwarf perch * Micrometrus minimus (Gibbons) * Species previously not listed. t Not recorded from California. ± Gulf of California species introduced into Salton Sea. 0PPIC1 M. COM M'»\ MAM] 261 FAMILY POMACENTRID \i: Dame elf] b< Blacksmith Ghromia punctipinnis (Cooper) Garibaldi Hypsypops rubicunda (Girard) I'AMILN LABRIDAE Wro e Sheep-head Pimelometopon pulchrum (Ayr< > Formerly written "sheepshead." Changed to approximate •• closelj the pre- vailing pronunciation and to help distinguish this species from the unrelated marine and fresh-water fishes of eastern North America thai are known pud." (Rock) wrasse* Halichoeres semicinctus (Ayri I Sefiorita Otcyjulis californica (Gtlnther) FAMILY GIRELLIDAE Nibblers Opaleye - Oirella nigricans (Ayr< I FAMILY SCORPII>AF Ilall'im s Halfmoon \£edialuna californiensis (Steindachner) FAMILY SCORPAENIDAE Rockfishes Rocaccio Sebastodes paucispinis i Ayres) Chilipepper Sebastodes goodei Eigenmann i^ Eigenmann Blue rockfish Sebastodes my stinus (Jordan & Gilbert) The "hook name" priestfish was formerly applied to this fish bul did aol enter the vernacular. The new name reflects considerable usage. Olive rockfish * Sebastodes serranoides Eigenmann vV Eigen- mann Yellowtail rockfish Sebastodes fiavidus Ayres Black rockfish Sebastodes melanops (Girard) Orange rockfish Sebastodes pinniger (Gill) Vermilion rockfish Sebastodes miniatus i. Ionian & Gilbert i Kelp rockfish * Sebastodes at fori re us (Jordan & Gilberl i Speckled rockfish Sebastodes oralis Ayres Both this species and S. entomelas were formerly termed "'widow rockfish." Redstripe rockfish* Sebastodes proriger (Jordan & Gilbert) Widow rockfish Sebastodes entomelas (Jordan & Gilbert) Halfbanded rockfish* Sebastodes semicinctus Gilbert Honeycomb rockfish* Sebastodes umbrosus (Jordan & Gilbert) Rosy rockfish * Sebastodes rosaceus I Girard i Orange-red rockfish * Sebastodes helvomaculatus ( Ayres) Greenspotted rockfish Sebas1o Pink rockfish * Sebastodes cos Eigenmann & Eigenmann Starry rockfish Sebastodes constellatus (Jordan & Gilberl I Tambor * Sebastodes ruberrimus Cramer Flag rockfish* Sebastodes rubrivinctus (Jordan kV Gilbert) Greenstriped rockfish Sebastodes elongatus (Ayres) Brown rockfish* Sebastodes auriculatus (Girard) Grass rockfish * Sebastodes rastrelliger (Jordan & Gilberl i Whitebelly rockfish* Sebastodes vexillaris (Jordan & Gilbert) Copper rockfish * Sebastodes caurinus ( Richardson i Quillback rockfish * Sebastodes maliger i. Jordan & Gilbert) Black-and-yellow rockfish Sebastodes chrysomelas (Jordan & Gilbert) Gopher rockfish * Sebastodes camatus (Jordan & Gilbert i China rockfish Sebastodes nebulosus (Ayres) Treefish Sebastodes serriceps (Jordan & Gilberl i Blackhanded rockfish * Sebastodes nigrocinctus I Ayres) Sculpin Scorpaena guttata Girard "Scorpionfish" is recognized as an alternative name. Channel rockfish Sebastolobus alascanus Bean "Thornhead" is recognized as an alternative name. FAMILY ANOPLOPOMATIDAE— Sablefishes Sablefish : Inoplopoma fimbria i Pallas) "Blackcod" is recognized as an alternative name. * Species previously not listed. 262 CALIFORNIA FISH AND GAME FAMILY HEXAGRAMMIDAE— Greenlings Greenling seatrout Hexagrammos decagrammus (Pallas) "Kelp greenling" is recognized as an alternative name. Rock greenling * Hexagrammos superciliosus (Pallas) FAMILY OPHIODONTIDAE— Lingcods Lingcod Ophiodon elongatus Girard FAMILY COTTIDAE— Sculpins Cabezon Scorpaenichthys marmoratus (Ayres) Staghorn sculpin Leptocottus armatus Girard FAMILY GOBIIDAE— Gobies Mudsucker Gillichthys mirabilis Cooper FAMILY BATRACHOIDIDAE— Toadfishes Northern midshipman * Porichthys notatus Girard Slim midshipman * Porichthys myriaster Hubbs & Schultz FAMILY CLINIDAE— Klipfishes Kelpfish Heterostichus rostratus Girard FAMILY ANARHICHADIDAE— Wolffishes Wolf-eel Anarrhichthys ocellatus Ayres FAMILY CEBIDICHTHYIDAE— Monkeyfaces Monkeyface-eel Cebidichthys violaceus (Girard) Formerly, with Xiphister mucosas, "blenny-eel." Both are usually simply "eel" to fishermen. Official — in these cases, coined — names were considered desirable. FAMILY STICHAEIDAE— Pricklebacks Rock-eel Xiphister mucosus (Girard) See comment above. FAMILY MOLIDAE— Molas Mola Mola mola (Linnaeus) Formerly "ocean sunfish." "Mola" is used as much as, if not more than, "ocean sunfish" and is obviously more appropriate. REFERENCES American Fisheries Society 1948. A list of common and scientific names of the better known fishes of the United States and Canada. Amer. Fish. Soc, Spec. Publ. 1, 45 p. Godsil, H. C. and Edwin K. Holmberg 1950. A comparison of the bluefin tunas, genus Thunnus, from New England, Aus- tralia and California. Calif. Div. Fish and Game, Fish Bull. 77, 55 p. Roedel, Phil M. 1948. Common marine fishes of California. Calif. Div. Fish and Game, Fish Bull. 68, 150 p. 1949. Common names. Calif. Div. Fish and Game, Fish Bull. 74, p. 204-206. Roedel, Phil M., and "\Vm. Ellis Ripley 1950. California sharks and rays. Calif. Div. Fish and Game, Fish Bull. 75, 88 p. Shapovalov, Leo, and William A. Dill 1950. A check list of the fresh-water and anadromous fishes of California. Calif. Fish and Game, vol. 36, no. 4, p. 382-391. Walford, Lionel A. 1931. Handbook of common commercial and game fishes of California. Calif. Div. Fish and Game, Fish Bull. 28, 183 p. 1935. The sharks and rays of California. Calif. Div. Fish and Game, Fish Bull. 45, 66 p. • Species previously not listed. NOTES NEW RECORDS OF PACIFIC SARDINE AND PACIFIC MACKEREL IN THE GULF OF CALIFORNIA Published records for the Pacific sardine I Sardinops cat nth a include many localities in the Chili' of California, lint they are all confined to the western shores. In recent years tuna fishermen have reported catching sardines in bait hauls made near Guaymas on the eastern side, bul no specimens from this locality have appeared £or positive identification. The following records are of considerable interest, therefore, since they estab- lish the presence of the California sardine on the mainland side of tin- gulf, and also indicate that it may at times occur there in some abundance. Pish collections were made in the vicinity of Guaymas, Sonora, Mexico, in 1950, 1951 and 1952 by collectors from the Zoology Department, Uni- versity of California at Los Angeles. In 1950, although the area was covered intensively from January 20th until February 2d, no sardines were taken. In 1951 this area was sampled January 16th to 18th and February 8th and 9th. During this time only five specimens of Sardinops were taken, all at Puerto San Carlos near Guaymas, two I 29 and 35 mm. long) on January 18th and three (24-29 mm. long) on February 9th. These post-larvae were found off rocky shores and no schools of sardines were seen. No specimens were taken while seining. Mr. Norman Wilimovsky and Mr. Giles Mead of Stanford University surveyed this same area from May 27 through June 6, 1951. They col- lected Sardinops twice, both times taking many specimens, and report., 1 seeing large schools of sardines about two to three inches in lengi h. In 1952 the University of California expedition again collected in the Guaymas area intensively from January 24th through February 12th. In contrast to the two former years, over a thousand specimens were taken in eight different collections, all in the vicinity of Puerto San Carlos. In addition, post-larval stages of Sardinops were observed in large num- bers in the Puerto San Carlos area. The only adults seen were some dried specimens on the beach near Guaymas. These had been dumped from the bait basket of a market fisherman camped there, lie reported that this kind of "sardina" was common there and that he caught them often in his throw net. Although no intensive survey for sardines was made during any of our collecting, I am quite certain that these scanty data indicate a real dif- ference in abundance of young sardines for the dates mentioned. The methods of collecting and scouting were practically identical each year, and there seems little possibility that sardines should have appeared so rare during late January and early February in 1950 and 1951 and yet actually been present in the numbers observed in 1952. No reason for the ( 263 ) 264 CALIFORNIA FISH AND GAME apparent change can be determined at this time, since there is practically no hydro-graphic data available for this area. It is interesting to note, how- ever, that the surface temperatures averaged about 16 degrees C. during 1950 and 1951 and about 18 degrees C. in 1952. A Pacific mackerel {Pneumatophorus japonicus diego) was taken at Guaymas, Sonora, Mexico, on January 24, 1952. This single specimen, 294 mm. in standard length, was found in a fisherman's bait basket. It had been caught with a throw net and the fisherman reported that he often took them in this manner. This is the first record of the Pacific mackerel on the eastern side of the Gulf of California. Fitch (1952, p. 560) recently reported the taking of a young specimen from about 60 miles west of Mazatlan. Fowler (1944, p. 384) reports young of Scomber colias from 20 miles south of Mazatlan and from 22° 03' N. Lat., 106° 42' W. Long. These fish are almost certainly the same species identified here as Pneuma- tophorus japonicus diego and should constitute the published southern record for this subspecies. The specimens of Scomber colias reported by Fowler (op. cit.) from the Panama and the Galapagos are probably of the southeastern Pacific subspecies, Pneumatophorus japonicus peruanus, but the identity must remain in doubt until they have been re-examined. The whole question of the distribution of Pneumatophorus south of Cape San Lucas, Baja California, and the relationship of the populations, is urgently in need of study. REFERENCES Fitch, John E. 1952. Distributional notes on some Pacific coast marine fishes. Calif. Fish and Game, vol. 38, no. 4, p. 557-566. FoAvler, Henry W. 1944. The fishes. In Results of the Fifth George Vanderbilt Expedition (1941). Acad. Nat. Sci., Phila. Monogs., no. 6, p. 57-529. — Boyd W. Walker, Department of Zoology, University of California, Los Angeles, October, 1952. SURVIVAL OF SOME FISHES RECENTLY INTRODUCED INTO THE SALTON SEA, CALIFORNIA The terrific increase in angling pressure in Southern California calls for the full utilization of all waters in the area; the potentials for a marine sport fishery in the Salton Sea, if realized, could make a sub- stantial contribution. California's largest inland body of water lies in Riverside and Im- perial Counties, about 150 miles southeast of Los Angeles. The Salton Sea is about 13 miles wide by 32 miles long with an area of approxi- mately 275 square miles. At present the surface level is at minus 237 feet HSL. It is a shallow body of water, averaging no more than 15 feet deep with a few "holes" up to 60 feet deep. Two rivers, the Alamo and New, formed mainly from waste irrigation water, enter the sea from the south. The salinity of the Salton Sea approximates that of sea water. No outlet exists, but the 78-inch annual evaporation rate in this arid climate has maintained the sea at a fairly constant level. Prior to 1948 the only fishes present in the Salton Sea proper were the striped mullet {Mugil cephalus), the mosquitofish {Gambusia ajfinis), NOTE 1 he desert j)ii|ilisli ( < ' y pri notion macularius) , and possibly a I'-v. "die- hard" ten-pounders I Elops affinis i . Near the mouths of the Alamo and New Rivers a few fresh-water fishes, mainlj carp Cyprinu carpio . . found. In the summer of 1951, seining checks bj Departmenl of Pish and (lame personnel indicated that the mudsucker (Gillichthys mn had become well established, as all size ranges were found around tie- periphery of the Sal ton Sea. The presence of this species cannol l"- traced to any definite introduction, hut ii has been rumored thai Bome of the mullet fishermen had been attempting to raise such bail fish in the mar gina] areas of the sea and that corrosion of the containers permitted them to escape. Since 1948 four expeditions have been conducted to San Felipe, ico, on the western shores of the Gulf of California, by the California Department, of Fish and Game to procure marine game and forage fishes J'or experimental plaids in the Saltou Sea. Approximately ID, PUD Mich fish, of many kinds, have now been planted in this body of water. In 195:2 several recoveries of these fishes were made, as listed below. On January 17, 1952, a 22-inch orangemout h corvina I Cynoscion xan- tlnilus) was caught in a gill net by mullet fisherman J. II. Bible, in the southern end of the sea between Mullet Island and the new mouth (2.5 miles south of the old mouth) of the Alamo River, in " very shallow- water." It was estimated, to weigh between four and six pounds a1 time of capture. This fish represents one of the original introductions made either in May 1950 or March 1951. On July 11, 1952, a lf-inch croaker (Bairdiella icistius) was found alive along the east-central shore of the Salton Sea near the Riverside- Imperial county line near Durmicl Siding by Jack Bechtel of the Depart- ment of Fish and Game. Wave action had washed ii ashore. This was very likely the spawn of individuals from either the May 1950 or the March 1951 plants. On August 29, 1952, 11 Bairdiella 2.7-4.0 inches long were dip-netted by H. E. Schnarr, Chief of the Security Guard, U. S. Salton Sea B; at our request. These were found along the water surface at nighl at the base dock. On September 4 and 5, 1952, extensive trawling and beach-seining was carried out over representative sections of the Salton Sea by state biolo- gists. Many young Bairdiella 2.5-6.5 inches long were found alone- the west shore and at one point on the east-central side (125 per 1 DO- foot bag seine haul). This indicates that the original plants of adult Bairdiella, consisting of 57 individuals in 1950 and about two dozen in 1951, have successfully reproduced in the Salton Sea. Such evidence of the successful establishment of these marine fishes in the Salton Sea gives great hope for the development of a future -port fishery, provided that food supplies hold up under concentrated preda- tion on the naturally present desert pupfish, mosquitofish, marine worms, and plankton, or that new food organisms can be introduced. — P. A. Douglas, Bureau of Fish Conservation, California Department of Fish and Game, October 1952. 266 CALIFORNIA FISH AND GAME THE BRAMBLE SHARK (ECHINORHINUS BRUCUS) AT GUADALUPE ISLAND, MEXICO During the early part of the night of September 8, 1952, two large bramble sharks were taken at the northeast anchorage, Guadalupe Island, on the yacht Goodwill. Both were hooked and landed with rod and reel. Dead Mexican scads (Decapterus hypodus) were being used for bait and were fished near the bottom in 120 feet of water. The first shark, 267 cm. from the tip of the snout to the tip of the dorsal lobe of the tail, weighed 425 pounds. The second weighed 490 pounds and measured 295 cm. The weights were taken with a large balance scale and the measurements were straight line distances taken with a steel tape. Measurements appear below. Specimen 1 Specimen 2 cm. inches cm. inches Total length, tip of snout to tip of longest lobe of tail 267 105 295 116 Distance from tip of snout to insertion of pectoral fin 71 28 Distance from tip of snout to insertion of pelvic fin 160 63 Distance from tip of snout to origin of first dorsal 180 71 Interdorsal space 14 5£ Greatest girth 128 50i 148 58^ The fish, typical of previous descriptions of the species, had two small dorsal fins and no anal fin. The anterior dorsal fin originated just a little behind the insertion of the long-based pelvics. The skin was distinctly armed with isolated tuberculate scales, each with a hard stellate base and a small spine at the summit. Both sharks were females with ovarian eggs of two size classes ; small, 0.8 cm. or less in diameter, and large, approximating 3.3 cm. The 267 cm. specimen contained 114 of the large eggs. The displacement of 35 of these eggs, which had been preserved in 10 percent formalin, was measured and the average volume was found to be 19 cc. each. There were no signs of developing embryos. The stomach of the larger specimen was empty and that of the smaller contained only one large, almost wholly digested, gill arch. Late in August, 1952, Mr. R. C. Carpenter, skipper of the albacore troller Jon-tru caught what could only have been a bramble shark at the same locality (northeast anchorage, Guadalupe Island). This specimen was estimated to be six feet long and over 200 pounds. The bramble shark has been recorded from warm seas throughout the world but is nowhere plentiful. Three individuals have been recorded from California (Hubbs and Clark, Calif. Fish and Game, vol. 31, no. 1, p. 64-67, 1944). As far as is known, the 295 cm. Guadalupe specimen is the largest on record. — Robert D. Collyer, Bureau of Marine Fisheries, Department of Fish and Game, October, 1952. REVIEWS The Miami Conservancy District I5v Arthur E. Morgan; McGraw lliil Booh Company, [nc, S( ■••• fork, 1951 ; "xiii + 504 p. $0.50. About forty years ago the City of Dayton, Ohio, was almost wiped onf bj a flood, the most severe the city had ever known. .Mine than ■".<>(• people losl their li\'- and property damage exceeded $100,000,000 bul these figur< onlj a hint of actual horror and destruction. In the years which followed a more ignificanl was written by the people of that area themselves, as they worked and foilghl tO achieve permanent control of the wild Miami River and its tributarii D never again been plagued with floods. Mr. Morgan's hook is both a history and a text. It is thorough in its details, bat it often reads like pure drama. Starting with a background of past floods and the unwise economy of half measures proposed by sell appointed experts I" mini- the constant threat of floods, the book builds up to an early climax when the "Gl Flood of 1913" hits the city. The rest is a complete story of the tremendous effort over nine years (1914-1922) to formulate a practical flood control plan, and to it through to the point of finished construction and actual working condition. .Mainte- nance and further developments through 1!)47 conclude the hook. One of the outstanding features of the story is the vivid portrayal of how a demo- cratic people solved a very tough problem. Only through a combination of dynamic leadership, honest social cooperation and democratic action was the plan finished and the engineering job completed. Here, then, is a tribute to the people of the Miami River Valley and a monument to the leaders, not the bast of whom was Mr. Morgan, the chief engineer. The story is augmented by numerous biographies ami portraits of persons who contributed to the program, and by many newspaper excerpts which mention dates, names and places. Of particular interest is the description of the major role played by a big national industry, both in relief after the flood and in the over-all execution of the plan. This volume brings out several other things which are worth noting. Among them is the fact that many present projects of the Department of Fish and Game present problems similar to those which were recognized and handled by the .Miami Con servancy District. Especially pointed out is the danger inherent in a lack of sufficient publicity and proper public relations. An uninformed or suspicious public, led by armchair lawyers and "I've lived here all my life" characters, can block any program. One way in which Mr. Morgan overcame this resistance to the regional improvement project was to show the existence of a precedent. Precedents were not always right at hand, and often long and laborious research was required to dig them up. Never- theless, they were well worth discovering because they helped to sell the so-called practical man who places so much weight upon this matter of example. At the same time, complaints were received from the public because of the lengthy hut necessary period of gathering preliminary data, doing research and formulating the master plan. The question which seemed everywhere to confront the staff was "Why don't you do something?" How familiar that question sounds to many professional fish and game men ! Another section of the book describes the legislative problems confronting any new venture. The public-spirited reader may be appalled to note the stall's need to resort to many very intricate legal maneuvers in order to accomplish a straightfor- ward project for the public good — a project which apparent^ could cause absolutely no one any harm. Also of interest is Mr. Morgan's discussion of personnel selection and employee welfare. Today we accept such tools and principles as commonplace, but to apply them to engineering personnel in 1014 was almost revolutionary. This book is exceptionally well-documented, containing an annotated bibliography of 114 titles, an index of names and a general index. In addition, there are 104 photographs, including portraits, four maps, two graphs and six diagrams. ( 207 ) 268 CALIFORNIA FISH AND GAME "The Miami Conservancy District" is not recreational reading. Those who are interested in history, biography, and social documents, however, will find pleasure in going through this book. For the engineer, the subject matter will be old, but it will also be complete and under one cover. Persons in the field of conservation will find much of interest and benefit regarding water problems, even though the Miami River Valley may be far from their particular geographical location. Unfortunately, there will be many people to whom the text-like presentation of some features and the inclusion of exhaustive quotes and reproductions will be boring or objectionable. Others will like the infinite small personal touches and the sincere interest the author has in human beings, per se. I feel that the book is important as a social record, as a statement of high engineering achievement and as an interesting account of an historical event. — Herbert E. Pintler, California Department of Fish and Game. Freshwater Fishery Biology By Karl F. Lagler ; Wm. C. Brown Company, Dubuque, Iowa, 1952 ; x -f 360 p., illustrated. $5.75. Dr. Lagler has extensively overhauled his well-known earlier "Studies in Fresh- water Fishery Biology," which was first published in 1947 and passed through several editions, to produce the present comprehensive text and reference work for students and professional workers in the field. The book deals with the principles and methods of modern fishery research and man- agement of the inland waters of North America. The 25 chapters of the book treat suc- cessively natural history and ecology, classification, identification, the literature of fish and fisheries, anatomy, embryology and subsequent life history stages, food, age and growth, populations, yield, pathology, pollution, laws, fish culture, fishery sur- veys, improvement of inland waters, creation of new fishing waters, and inland com- mercial and recreational fisheries. Numerous fish scale photographs, reproductions of fishery survey forms, a list of abbreviations, a tabular summary of some important fish diseases, and conversion tables comprise the appendices. The individual chapters are followed by lists of references, and the book is amply illustrated by 184 figures. There is no doubt but that there has existed a pressing need for a publication of this kind in the relatively new field of fresh-water fishery biology. Dr. Lagler's book goes far toward meeting this need, although certain deficiences appear to be present to this reviewer, as described herewith. The attempt to provide both a reference for professional workers and a study out- line for students is evident and carried out by design (p. 15 and subsequent pages). In the opinion of the reviewer, this dual approach does not always work out as a happy combination. Certainly, the professional worker will often remain unsatisfied with the scope of treatment given a particular phase or subject. As an example of the above, there is not enough detail and discussion of "Electro- fishing" for the professional worker (pp. 8-10). The same comment applies to "Poison- ing" (p. 10) ; a scant paragraph is devoted to this important study and management tool and there is no discussion of methods of application or results obtained, and no references to it are cited. The selection of references appears to be quite uneven. Those cited at the end of each chapter are sometimes, but by no means always, the most significant or authori- tative ones for the field. Some apparently were selected only to illustrate some point in the text. It is not apparent why bibliographies such as Allen, "A selected bibli- ography of marine bionomics and fishery investigations," Baughman, "An annotated bibliography of oysters with pertinent material on mussels and other shellfish and an appendix on pollution," Corwin, "A bibliography of the tunas," and Wheeler, "A bibliography of the sardines" are cited in a book on fresh-water fishery biology. There are some important omissions (e.g., the O. W. A. A. check list of common and scientific names from p. 37). Also, the references are sometimes inaccurately cited and difficult to locale. No1 a single reference is cited at the end of Chapter V, "Fish Anatomy." It is evident that large segments of the book are based on the fishes and practices in the norfeh-central states. Discussion of important work done in the western United Slates is neglected and most western references are completely ignored. For example, in the chapter on "Stream Improvement," pp. 262-271, no mention is made of the con- struction of flow maintenance dams, stream clearance, or other practices and prob- lems of western waters. There is casual mention but no discussion of fishways, a sub- ject of great importance in western North America. Some common and representative far western fishes, e.g., all members of the genera Hesperoleucus and Siphateles, Coi- tus asper, gulosus, and aleuticus, the eulachon, Thaleicthys pacifieus, the tidewater goby, Eucyclogohius neivberryi, and the striped bass are all omitted from the check REVIEWS '-''''l list of "common and representative freshwater ti he of North America, north of Mexico" (p. lil 36). Unfortunately, mans methods described in older work are rather often cited without .1 critical analysis in the light of later finding . Farm ponds, which have created many problems for fishery biologists in many sections of the I uited States, are treated quite briefij and casually (p. 274 275). Prom n reading of the text ii is evident thai standardization in method , prooedun and terminologj in the field of fresh-water fishery biology is -till far from realized (e.g., s.T p. 109) . in the opinion uf the reviewer, the .- 1 < - 1 1 1 .- 1 ( illustration of manj type of blanl used in inland fishery investigations is a very useful feature of the book. I n brief summary, ii may be stated thai this book is a valuable compendium of many commonly used methods and practices of fresh water fisherj biology in the United States, which could be made even more useful to both student and professional worker if broadened to include certain neglected phases of the field, augmented to include im portant work done in i he West, and supplemented with critical analj <■- of certain -till accepted bul outdated methods and practices. Leo Shapovalov, California Depart men I of Fish a ">n page K»!». (2) Misidentifications : Page 73, figure 1. is Chione gnidia, not C. undatella; figure (I. same page, is ('. undatella, not 0. calif orniensis ; page 97, figures I. 5, and <".. labelled Parapholas californica, Barnea pacifica and Bankia are Parapholas acuminata, Pent- tella penita and Xylophaga; on color plate 4 and black and white plate 30, figures 11 and 1!) are not ('onus calif ornicus ; on black and white plate 21. Opalia wrobletcskii and Epitonium boreale are synonymous, hut figures 1 and 6 are Opalia chacei; and. on page 136, figure 7 should be Pterynotus rhyssa. (3) Poorly chosen common names, most noticeable of which are the names given by the author to several important California (Pacific Coast I species which are regu- lated by law and have had common names assigned to them for years. Among these: "blue" abalone for our green abalone and "corrugated" for our pink abalone; "giant pod" for Siliqua ptttula, which has had several volumes written on it and is commer- cially canned as the "Northern razor clam" or just "razor clam" ; "Nuttall's saxidome" for our commercial "Washington clam" and "Washington clam" for the gaper. I am sure that no California clam digger would recognize the bean clam under the name "Goulds wedge" nor the bent-nose clam by the name "common macoma." (4) Obvious poor descriptions: For Ualiotis fulgens the statement "there are gen- erally six open holes near the margin plus a notch at th Ige." yet the illustrations on pages 2S and 100 show hut five, which is as it should he ; for If. cracherodi, the typical number is given as 8, the figures show 5 and 7 respectively 7 is most typical; for If. rufescens I he number is given as 4, the figures show .". and " it should he ; the ante- rior and posterior sculpture mentioned for Zirfaea pilsbryi should be reversed and Amiantis callosa does have a periostracum, is not pure white, on account of the very grey periostracum, and the concentric ridges frequently divide near the center of the shell. 270 CALIFORNIA FISH AND GAME (5) Among the wrong habitats and ranges : Chione fluctifraga is typically found in gooey, black mud rather than sand, just below high or mid-tide level rather than low tide and is much more common than C. undatella; Lithophaga plumula often bores into large dead shells, but more often into live shells and I question including Chama among these ; Mya arenaria is found quite commonly from Elkhorn Slough at least to the Oregon border and not just in San Francisco Bay ; Schizothaerus nuttalli prob- ably ranges into British Columbia, it definitely does not stop at Bolinas Bay, and Pecten diegensis ranges several hundred miles south of San Diego. A book such as this is definitely needed on our coast and it is certainly a shame there had to be such an inexcusable number of mistakes as appear in this volume. It is hoped that the book will be thoroughly revised in the very near future. — John E. Fitch, California Department of Fish and Game. The Ocean River By Henry Chapin and F. G. Walton Smith ; Charles Scribner's Sons, New York, 1952 ; viii + 325 p., illustrated. $3.50. This recent addition to the list of books about the science of the sea designed for the layman deserves high rank in the group. It is concerned almost entirely with the North Atlantic and its central theme is the Gulf Stream — the Ocean River. As one would expect, it presents the scientific story in terms of geology, oceanography, and biology, with an explanation of the dynamics of this great system. Beyond that, the reader learns of the influence of the "river" on civilizations bordering the Atlantic and, particularly fascinating, the story of Atlantic explorations from the beginning of recorded history. Chapin, historian and anthropologist, and Smith, oceanographer and biologist, make a good team and get the most out of their subject. Our Amazing Birds: The Liitle-known Facfs About Their Private Lives By Robert S. Lemmon ; American Garden Guild and Doubleday & Co., New York, 1952 ; 239 p., illustrated in black and white by Don R. Eckelberry. $3.95. Dedicated "For bird watchers of all ages everywhere," this book contains illustra- tions and short discussions of 102 species of North American birds, species which the author regards as worthy, for one reason or another, of the adjective "amazing." The approach is strictly nontechnical, the text is well-written, and the paintings excellent. It is a handsome volume, a credit to the publisher, and one which the bird lover will likely want on his library shelf. REPORTS FISH CASES October, November, December, 1952 i Iffense Abalone: Undersize; overlimit ; baking without license; Failure to aho hell; no measuring device ..- Angling: No license; possessing spear near Bel River; more than one pole; angling closed waters; extra gear; fishing near dam; snagging; failure to show license; night fishing; using another's license; transferring license; operating aetline; fishing in fish ladder; illegal possession of gaff; possessing spear within 300 It. stream; unattended pole; false statement on license application; alien using citizen's license - Bass: Overlimit; undersize; mutilating: bringing illegally into State; taking with more th?n one rod; t iking without lire use; at night. Catfish: Overlimit ; taking without license Clam: ( 'ver limit ; undersize; failure to return to hole; using another's license; taking in refuge Commercial: Operating smokehouse without license; commercial fishing without license; untagged lobsters; dealer possessing lobster in closed season; und lobsters; using net in closed district; overlimit salmon; market lobsters in closed season; operating cannery without licensi : no CO] license; no boat registration; waste of fish by packers; selling fish taken from boat carrying anglers; possession of sea bass on purse seiner; using roundhaul net District 20; selling untagged salmon; possessing trawl under 4'_> inches; selling fresh salmon and steelhead spawn; undersize crabs; sale undersize skipjack Crab: Closed seas »n; t iking females Frog: Overlimit; taking in closed season Lobster: Using traps in District 19A; undersize; closed season; using aqualung Mullet : Spearing Perch : Overlimit Pollution: Oil Salmon: Spearing; snagging; taking from spawning beds; taking from cl stream: with gaff; at night; possession spear near spawning bed; possessing illegally and failing to show; no license; using 2 pcles; shooting; cl >sed season... Sunfish: Overlimit; nc license; taking closed season Trout: No license; taking with net; overlimit; nc permit and transporting; closed season; transporting illegally into State; taking in closed area Total. Sale of seized fish . Grand total 27 313 .' 102 69 2 :• 9 1 1 7 62 .' 32 696 • 1,115.00 3,022 m, 75 it" - ! ■ $19.7 ! 1,94 • 10 10 -- - • ( 271 ) 272 CALIFORNIA FISH AND GAME GAME CASES October, November, December, 1952 Offense Number of arrests Fines imposed Jail sentences (days) Bear: Canning gun in State park and attempting to trap bear in closed season; trapping and killing in closed season ; taking at night Coot: Late shooting; taking from powerboat with 22 rifle; taking without license.. Deer: Failing to fill out tags; failing to retain skin and antlers; carrying extra tag and using another's tag; hunting without tags; possession untagged deer; killing in closed season; taking doe; possession artificial light and spike buck; using Utah residence license; transporting illegally; possession without permit; shooting in safety zone; taking in refuge; using "A" tag in one deer district; night hunting; shooting within 150 yds. dwelling; passing first validating officer; using illegal ammunition; possession doe and fawn; shooting from car; failure to close gate while hunting; transferring tag to another; taking deer in possession of another; taking forked horn in closed season; overlimit; possessing illegally Deer Meat: Possessing meat taken in closed season ; possessing unstamped meat in freezer; meat of doe; selling Dove: Taking closed seascn; overlimit; without license; shooting with unplugged gun ; transferring shipping tag ; shooting from car ; taking with 22 rifle ; hunting from car; using unplugged gun Duck: Late shooting; early shooting; from powerboat; possession gun in refuge; using unplugged gun; no stamp; overlimit; using 22 rifle; taking in refuge; with- out license; in cooperative area without permit; illegal transportation; closed season; possession without evidence of species Elk: Possessing elk meat; no license; no permit; taking fully protected animal Goose: Overlimit; late shooting; using unplugged gun; nonresident hunting with illegal license ; shooting in refuge ; without license Hunting: Possessing gun in refuge; trespass in closed zone; hunting without license; shooting across highway; using unplugged gun; failure to procure nonresident license; spotlighting; transferring hunting license; shooting within 50 ft. of dwelling; failure to show license; shooting on public road; night hunting Loaded gun in car Mudhen: Herding with powerboat; taking with 22 rifle and no license Nongame birds: Shooting marsh hawks from highway; taking glossy ibis; swan; robin; shorebirds; seagull; plover Pheasant: Taking closed season; taking hen; without license; trespass in pheasant cooperative; on cooperative area without back tag; failing to tag; using another's license and tags; using unplugged gun; overlimit; hunting closed zone; late shoot- ing; early shooting; possessing pheasant without plumage; shooting near dwell- ing; possession and transporting illegally; shooting from road; with 22 rifle; taking eggs and raising without breeder's license Pigeon: Taking closed season; using unplugged gun; no license Quail: Hunting without license; using unplugged gun; taking in closed season; overlimit; hunting on cooperative area without permit; bringing illegally into California from Mexico; taking in refuge; shooting from highway; shooting with 22 rifle Rabbit: Taking with unplugged gun; closed season; night hunting; spotlighting; without license; taking and failing to show license; early shooting Sagehen: Taking closed season; failure to show Sierra Hare: Taking closed season Squirrel: Taking closed season; transporting illegally Totals . 333 40 45 435 4 32 113 682 4 19 359 3 46 58 2 1 3 2,188 S850.00 150.00 28,320.00 2,210.00 1,625.00 12,912.00 325.00 1,065.00 4,126.00 16,515.00 110.00 525.00 15,576.50 155.00 1,730.00 2,115.00 100.00 15.00 150.00 500 705 83 888,574.50 1,293 KKI-Oin'S SEIZURES OF FISH AND GAME October, November, December, 1952 • Fish: A I alone Bass Catfish Chun Crab Frog... Lobster.... Mackerel, jack. Mullet Perch Salmon. Sardine.. Sunfish Trout Tuna Game: Bear Coot Deer Dove Duck Elk Goose Nongame birds. Pheasant Partridge Quail Pigeon Rabbit Sagehen Squirrel 140 '. 149 1 168 1 74 16 1 26 49 1 9 140 printed in camfornia state printing OFFICE 71944 12-52 7,500