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International Journal of Fisheries Science and Research

Delayed Fertilization of Landlocked Fall Chinook Salmon Eggs Stored with Oxygen at Two Temperatures

Abstract Citation Introduction Materials and Methods Results Discussion Conclusion Acknowledgement References
Details

Received: 11-Feb-2019

Accepted: 11-Mar-2019

Published: 14-Mar-2019

Hunter Eide and Michael E Barnes*

McNenny State Fish Hatchery South Dakota Department of Game, Fish and Parks Spearfish, South Dakota State University, United States

Corresponding Author:

Michael E Barnes, McNenny State Fish Hatchery, South Dakota Department of Game, Fish and Parks Spearfish, South Dakota, United States, Tel:605-642-1262

Keywords

Chinook salmon; Oncorhynchus tshawytscha; Egg storage; Delayed fertilization

Abstract

This study examined the use of supplemental oxygen and two temperatures (1° and 11°C) during the four hour storage of unfertilized landlocked fall Chinook salmon (Oncorhynchus tshawytscha) eggs from Lake Oahe, South Dakota, USA. There was a significant and positive effect of oxygen use on egg survival to the eyed-stage and hatch. In addition, survival to egg eye-up and hatch was significantly affected by storage temperature, with decreased survival at 1°C. However, there was no significant interaction observed between the use of oxygen and storage temperature. Mean survival to hatch ranged from 50% for those eggs stored with oxygen at 11°C compared 17.8% for those eggs stored on ice at 1°C in air. To maintain landlocked Chinook salmon egg fertility, storage with supplemental oxygen at 11°C is recommended.

Citation

Eide H and Barnes ME. Delayed Fertilization of Landlocked Fall Chinook Salmon Eggs Stored with Oxygen at Two Temperatures. Int J Fisheries Sci Res. 2019; 3(1): 1011.

Introduction

While fertilization frequently occurs immediately during artificial spawning of trout and salmon, gametes can also be stored for use at a later time [1]. Delayed fertilization may be done in an attempt to increase egg survival or to improve the efficiencies of spawning operations, particularly if spawning occurs far from incubating hatcheries [2-6].

Successful egg storage prior to fertilization has been shown to be influenced by the amount of time the eggs are stored and the storage temperature [2]. In one of the earliest studies involving salmonids, sockeye salmon (Oncorhynchus nerka) unfertilized eggs were successfully stored without any loss of fertility at temperatures of 5°C for 25 hours, but decreased fertility was noted in eggs stored at either 8°C and 11°C [7]. Withler and Morley [8] observed that unfertilized sockeye salmon eggs could be stored at temperatures of either 2.9°C or 9.9°C for up to 22 hours without any loss of fertility. However, after 70 hours of storage, fertility decreased by over 50%, but only during storage at 9.9°C. Similarly, unfertilized pink salmon (O. gorbuscha) eggs stored at 8.5°C experienced declining fertility after only eight hours of storage, while those at 3.2°C maintained egg fertility over five times longer (46 hours). Poon and Johnson [2] also found pink salmon eggs remained fertile for up to six hours after removal from female broodstock when stored at 6°C. Jensen and Alderdice [9] reported a negative relationship between egg storage time and temperature with unfertilized chum salmon (O. keta) eggs, with egg fertility remaining for up to 124 hours at 3°C storage temperatures, and Ginatullina et al [6], successfully stored unfertilized rainbow trout (O. mykiss) eggs at 2°C for 20 hours. However, fall Chinook salmon (O. tshawytscha) eggs may be particularly sensitive to storage time and temperature, with 47% mortality observed from eggs stored at 1°C for 48 hours [10].

Unlike milt, which is typically stored with the air replaced by gaseous oxygen [11], fish eggs are generally stored in ovarian fluid with air. However, significant increases in fertility have been observed with Mozambique tilapia (Oreochromis mossambicus) eggs stored for 20 hours in oxygenated conditions compared to just air [12].

Lake Oahe, South Dakota, USA, contains a relatively unique population of landlocked fall Chinook salmon [13]. There is no natural reproduction in this population; it is maintained entirely artificial propagation [14]. Spawning occurs at Whitlocks Spawning Station adjacent to the lake, and fertilized and water-hardened eggs are then transported four hours to production hatcheries. Two studies have evaluated delayed fertilization of Lake Oahe salmon eggs. Barnes et al [15]. reported over a 50% drop in fertility when Lake Oahe salmon eggs were stored for only four hours. More recently, Eide and Barnes [16] also documented that fertilization was impaired when Lake Oahe salmon egg fertilization was delayed for four hours, but noted that egg fertility was maintained for up to two hours. Neither Barnes et al [15] nor Eide and Barnes [16] evaluated the impact of different storage temperatures or oxygen on Lake Oahe Chinook salmon egg storage. Thus, the objective of this study was to determine if decreased storage temperatures and the addition of oxygen could allow such eggs to maintain fertility for up to four hours.

Materials and Methods

Landlocked fall Chinook salmon from Lake Oahe were spawned at Whitlocks Spawning Station, near Gettysburg, South Dakota, USA on October 10, 2018. Milt was collected from males, pooled in a container, and approximately 50 ml placed into a 0.95 L plastic bag. Oxygen was added to the bag prior to sealing and then it was placed on ice until used. Eggs from five female salmon were pneumatically-expressed using compressed oxygen. These eggs were then combined into a common pool, with 450 eggs removed for experimentation. The 450-egg group was further divided into 15-egg samples, with each sample placed into its own discrete 0.95 L plastic bag.

A 2 x 2 experimental design was used. With the exception of six egg bags that were fertilized immediately, all of the egg samples were stored for four hours prior to fertilization. The treatments were either stored at 11°C or with ice (approximately 1°C), with the bags either containing air or having the air replaced with compressed oxygen (six bags per treatment; N = 6). Egg fertilization occurred by adding one ml of milt to each bag. Lake water (total hardness as CaCo3, 210mg/L; pH, 7.6; total dissolved solids, 390mg/L) was then added to the egg/ milt mixture for sperm activation.

After approximately one minute, the eggs were rinsed, with each bag of eggs placed into a discrete 9.5-cm plastic Petri dish filled with 30 ml of water. The dishes were incubated in an Insignia model NS-WC16BK6 refrigeration unit (Best Buy, Richfield, Minnesota, USA) at 10°C through complete hatch using the technique described by Neumiller et al [17]. Dead eggs and fry were manually removed and counted when the water was changed. Fry were also removed and counted after hatch. The following formulas were used to determine percent survival: Survival to Eyed-Egg Stage (%) =100 x (number of eyed eggs/initial egg number); Survival to Hatch (%) =100 x (number of hatched fry/initial egg number).

Data was analyzed by two-way analysis of variance using the SPSS (9.0) statistical analysis program (SPSS, Chicago, Illinois, USA). Significance was predetermined at P<0.05. Percentage data was log transformed to stabilize the variances [18].

Results

There was a significant and positive effect of oxygen use on survival to the eyed-stage and hatch (Table 1). In addition, survival to egg eye-up and hatch was significantly affected by storage temperature, with decreased survival at 1°C (Table 2). However, there was no significant interaction observed between the use of oxygen and storage temperature with survival to the eyed-stage (P = 0.922) or hatch (P = 0.804). Mean survival to hatch ranged from 50% for those eggs stored with oxygen at 11°C compared 17.8% for those eggs stored on ice at 1°C in air (Table 3).

Table 1: Mean (SE) percent survival to egg eye-up and fry hatch of landlocked Chinook salmon eggs fertilized immediately after spawning (control) or stored for four hours prior to fertilization in bags containing either air or compressed oxygen (N = 12, except for the control where N = 6).

 

    Oxygen  
  Control Yes No P
Eye (%) 43.3 (4.5) 46.1 (5.3) 26.7 (4.0) 0.003
Hatch (%) 42.2 (4.1) 43.3 (5.9) 26.1 (3.9) 0.004

Table 2: Mean (SE) percent survival to egg eye-up and fry hatch of landlocked Chinook salmon eggs fertilized immediately after spawning (control) or stored for four hours prior to fertilization at either 1°C (on ice) or 11°C (N = 12, except for the control where N = 6).

    Temperature  
  Control 1°C 11°C P
Eye (%) 43.3 (4.5) 27.2 (4.5) 45.6 (5.0) 0.017
Hatch (%) 42.2 (4.1) 27.2 (4.5) 42.2 (5.8) 0.035

Table 3: Mean (SE) percent survival to egg eye-up and fry hatch of landlocked Chinook salmon eggs stored for four hours prior to fertilization in bags containing either air or compressed oxygen and at one of two temperatures (N = 6).

Oxygen Temperature Eye (%) Hatch (%)
Yes 11°C 55.6 (8.0) 50.0 (10.7)
Yes 1°C 36.7 (4.8) 36.7 (4.8)
No 11°C 35.6 (2.8) 34.4 (2.7)
No 1°C 17.8 (5.6) 17.8 (5.6)

Discussion

The results of this study describe for the first time the successful maintenance of landlocked Chinook salmon egg fertility after four hours of storage. Storing the eggs with supplemental oxygen was critical. Barnes et al [15] observed significantly decreased landlocked fall Chinook salmon egg fertility when the eggs were stored in air for four hours at undefined temperatures. Additionally, Eide and Barnes [16] also were unable to maintain landlocked Chinook salmon egg fertility after four hours of storage in air at 11°C. The results of this study, and those of Barnes et al [15] and Eide and Barnes [16], strongly suggest that using oxygen during egg storage for four hours is essential for successful fertilization. In the only other published study examining the use of oxygen during fish egg storage, Harvey and Kelley [12], also noted improvements in the fertility of tilapia eggs after 20 hours of storage prior to fertilization. In contrast to the landlocked fall Chinook salmon eggs used in this study, storage of other salmonid eggs without supplemental oxygen has generally been successful for durations much longer than four hours [2,6-9].

It is surprising that egg fertility was negatively related to storage temperature in this study. In general, colder temperatures are associated with longer salmonid egg storage times [2]. Numerous studies have documented that at lower temperatures ranging from 2°C to 5°C, salmonid egg fertility was unaffected for time frames of 22 to 124 hours, compared to declines in fertility at storage temperatures ranging from 8°C to 11°C [6-9]. However, Piper et al. [10] reported nearly 50% mortality in Chinook salmon eggs stored at 1°C for 48 hours. It is possible that the 1°C temperature used in this study was too cold, although Ginatullina et al [6], successfully stored unfertilized rainbow trout eggs at 2°C for 20 hours, and pink and chum salmon eggs have been successfully stored at temperatures close to 3°C [8,9].

While possible, it is unlikely that milt storage influenced the results of this study. Survival was similar among the control, immediately-fertilized, eggs and the eggs subjected to some of the delayed-fertilization treatments. Salmonid milt in general can be stored for over a month [19], and Chinook salmon milt in particular has been successfully stored for up to 14 days [20]. Sperm motility has been observed in milt from Lake Oahe Chinook salmon after short term storage on ice [21]. Indeed, the use of low temperatures [9,22] and supplemental oxygen [8, 23-25] in this study likely preclude any issues with sperm storage.

Although overall egg survival in this study was relatively low, it is normal for landlocked fall Chinook salmon eggs from Lake Oahe [13,26]. This introduced, totally-freshwater, population of Chinook salmon is relatively unique, with reproductive characteristics dramatically different than Chinook salmon in their native range [13,26]. This is likely why Lake Oahe Chinook salmon eggs do not exhibit the same response to storage and delayed fertilization as reported for other populations [1,10,16,26].

The successful fertilization of Lake Oahe salmon eggs after four hours of storage, enables the option of shipping gametes from the spawning station to the incubating hatcheries, as opposed to the current practice of immediate fertilization and subsequent shipment of water-hardened eggs [15]. However, disinfection of stored eggs and milt upon arrival at the hatcheries would need to occur [27]. Unlike the long-established techniques using iodophor solutions to disinfect of water-hardened eggs [28-30], potential protocols for gamete disinfection are currently unknown.

Conclusion

In this study documents for the first time the successful storage of Lake Oahe landlocked fall Chinook salmon eggs for four hours prior to fertilization by adding oxygen and maintaining temperatures at 11°C. Future experiments should determine how long eggs can be stored with supplemental oxygen, as well as the impact of different storage temperatures.

Acknowledgement

We thank Gerri Eide, Shon Eide, Robert Hanten, and the staff at Whitlocks Salmon Spawning Station for their assistance with this study.

References

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Effect of Fishmeal Substitution by Lima Bean Meal on the Zoo Technical Performances of African Catfish (Clarias gariepinus) in the Bati

A study on the effect of the substitution of fishmeal by Lima bean flour was conducted between March and May 2018 within the AIO ICG of the Batié District, with the global objective of contributing to the development of alternative sources of animal protein. Specifically, the aim of the study was to evaluate the effect of the substitution of fishmeal by Lima bean flour on the growth performance, survival and feed cost of Clarias gariepinus. For this purpose, 300 fry of Clarias gariepinus with an average weight of 3 ± 1.41g were divided into five batches and fed three times a day with rations corresponding to 5% of their ichthyo biomass. The rations R0, R25 R50, R75 and R100 respectively corresponded to the substitution rates of 0, 25, 50, 75 and 100% of fish meal by that of Lima bean. The physic-chemical characteristics of the water (pH, temperature, dissolved oxygen, nitrites and nitrates) were measured daily. The following results were obtained: The highest weight gains were obtained with the rations R25 (20.56 ± 0.40 g), R50 (20.64 ± 0.32 g), R75 (20.98 ± 0.46 g) and the lowest with the ration R100 (16.21 ± 0.28 g). For this average daily gain, the highest values were 0.36 ± 0.02 g; 0.37 ± 0.01 g, 0.38 ± 0.01 g respectively for the R0, R50 and R75 rations and the lowest with R100 (0.29 ± 0.01 g). The highest value of the specific growth rate (2.47 ± 0.07%) was obtained with the ration R0 and the lowest (1.61%) with the ration R100. The consumption index reached its highest and lowest values with the rations R100 (4.74 ± 0.42) and R50 (3.57 ± 0.43) respectively, compared to the value of the ration R0 (3.31 ± 0.37) for this parameter. Concerning the condition factor K, the highest value was recorded with the R50 diet (1.11 ± 0.49) while the lowest value was obtained with the R75 diet (0.95 ± 0.45). The cost of producing one kilogram of food was higher with the R25 ration (504.59 FCFA) and lower with the R100 ration (443.20 FCFA). This study found that incorporating 75% Lima bean flour into the feed increases the growth performance of Clarias gariepinus fry and reduces the cost of food production.

Emile Miégoué1*, Pégis Davy Tagning Zebaze2, Fernand Tendonkeng1, Lemoufouet Jules1, Nadège Elvire Njoh2, Ronald Komguep Nganyo2 and Etienne Tedonkeng Pamo1


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Comparative Effect of Monoculture and Polyculture in Two Species of Clariidae: Heterobranchus longifilis and Clarias gariepinus in Post Fingerlings Growth

In order to improve the production of Clariidae, a study on the type of cultivation of Heterobranchus longifilis and Clarias gariepinus in post fingerlings growth phase was carried out in tanks. It took place from March to May 2018 at the IRAD fish station in Koupa-Matapi (LN: 5º 21 ‘to 5º 58’ and LE: 10º 17 ‘to 11º 02’) west region Cameroon. For this fact 180 fry therefore 90 Heterobranchus longifilis and 90 Clarias gariepinus with an average weight 3.55 ± 0.68 g; 8.46 ± 0.41cm of total length and 7.37 ± 0.30 cm of standard length were used. The 180 fry were divided into three treatments of 60 individuals (T1 treatment: Clarias gariepinus, T2 treatment Heterobranchus longifilis and T3 treatment: Clarias gariepinus + Heterobranchus longifilis). Each treatment was repeated twice. The fish were fed twice per day at a rate of 10% of the ichthyobiomass readjusted each month after control fishing with a feed at 42% crude protein. From the results of this trial, it appears that unlike the higher mortality rates (11.66 ± 2.36%) recorded in monoculture Clarias gariepinus, the highest cannibalism rates were obtained in monoculture of Heterobranchus longifilis (13.33 ± 4.71%). The survival rate was not influenced by the type of culture. Nevertheless, the highest rate (94.44 ± 0.00%) was observed in Heterobranchus longifilis in polyculture. The highest growth values were recorded for C. gariepinus in polyculture and the weakest for H. longifilis in polyculture. For linear growth, the highest values were recorded in C. gariepinus in monoculture. In order to reduce the rate of cannibalism and mortalities in Clarias gariepinus and Heterobranchus longifilis in post f ingerlings growth phase, it is preferable to combine these two species.

Nana Towa Algrient¹, Nanmegni Rostand Romeo¹, Tonfackachille Peguy², Efole Ewoukem Thomas¹ and Jouokou Salifou²