Effect of Different Feeds on Growth and Survival of the Sergestid Shrimp Acetes vulgaris Hansen, 1919 (Decapoda: Sergestidae)

Abstract

The sergestid shrimp Acetes vulgaris has long been an important fishery species in estuaries and coastal waters along the Pang-Rad River, Rayong province, Thailand. In nature, this shrimp feeds on a wide range of food items, such as phytoplankton, zooplankton, algae, plant matter, debris, sand, and mud. The objective of this study was to compare different feeds on growth and survival of A. vulgaris reared in fiberglass tanks containing 70 m3 of seawater salinity 25 ppt over a period of 70 days. Individual shrimps were fed with four different types of feeds i.e., newly hatched Artemia (Ar), rotifer (Ro), newly hatched Artemia + rotifer (ArRo) and shrimp larvae commercial feed (SF). Results suggested that specific growth rates (both for body weight and body length) of shrimps reared with SF were not significantly different with treatment feed with Ar, ArRo and Ro (p ≥ 0.05). The survival rate of A. vulgaris did not vary significantly (p ≥ 0.05) among the Ar, Ro and ArRo treatments. However, the highest survival rate of shrimp (81.78% ± 3.08%) was observed in SF treatment and the percentage of survival rate was significantly different with treatment feed with Ar, Ro and ArRo (p ≤ 0.05). The findings reflected the ability of Acetes shrimps to consume diverse food types including both live feed and pelleted feed. Insights obtained from this research suggested that artificial feed can be as efficient as live feeds. This new knowledge is a needed addition to a currently lacking knowledge base for aquaculture of this Acetes species.

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Phudhom, A. , Hrimpeng, K. , Senanan, W. and Tangkrock-Olan, N. (2024) Effect of Different Feeds on Growth and Survival of the Sergestid Shrimp Acetes vulgaris Hansen, 1919 (Decapoda: Sergestidae). Agricultural Sciences, 15, 71-81. doi: 10.4236/as.2024.151005.

1. Introduction

The shrimps of the genus Acetes (Crustacea, Decapoda, Sergestidae) are small planktonic shrimps [1] with an average length of 10 - 40 mm and average weight of 0.2 - 0.5 g [2] . Recently, 14 species of Acetes have been recognized and distributed worldwide [3] . The Acetes shrimps live mainly in the estuaries and coastal water of the tropical and subtropical regions of the world [4] [5] . In nature, Acetes shrimps are the link between phytoplankton, zooplankton, and animals at higher trophic levels [6] . They are commercially important organism in Asian countries [7] and East African waters [8] . In 2021, the annual catches of Acetes in Thailand were 25,800 tons [9] .

The species Acetes vulgaris Hansen, 1919 occurs in estuaries and shallow coastal waters along the Gulf of Thailand and the Andaman Sea [10] . They are brackish and able to survive in salinity of 30 ppt or less, during certain seasons of the year [11] . They feed on a wide range of food items [12] . They eat several things like phytoplankton, zooplankton, algae, plant matter, debris, sand and mud [13] [14] [15] [16] . They are the most common species found along the coastal area of Rayong Province in Thailand [10] . This species is one of the most important commercial shrimp resources in Thailand and other countries in Asia [17] . In Thailand A. vulgaris is commercially exploited from July to September, using push nets [18] . The main uses of this shrimp are as fermented food, locally known as “Kapi” and as a dried product. It has also been used to feed larvae and adults of penaeid shrimps in aquaculture industry and laboratory [12] .

In comparison with the knowledge of distribution, taxonomy, ecology, and biology [19] [20] [21] little is known about the effect of different types of feeds on growth and survival of Acetes species. Since quality food and proper nutrition are key to the success of commercial shrimp culture, probably including Acetes species. Until now, there has been no study concerned about feeding of Acetes shrimps in Thailand. Thus, the objective of the present study is to investigate differences in growth and survival rates of A. vulgaris with respect to different feeds. The results of these studies could help to understand feeding ecology, aquaculture, and probably could also help to understand sustainable management of the Acetes shrimp resources in the near future.

2. Materials and Methods

2.1. Source of Shrimps and Experimental Design

A. vulgaris were collected from the estuarine areas of the Pang-Rad River (12˚41'49.9"N; 101˚47'10.8"E), Rayong Province. Shrimps were caught using an umbrella dip net shrimp with fine mesh size 2 × 2 mm. during the period of August to September 2018. The shrimps were transported in oxygenated polythene bag to the laboratory. Before experimentation, shrimps were reared in 2000 L concrete tank filled with seawater at 25 ppt under constant aeration and were acclimated for one week at ambient temperature of 27˚C - 29˚C. Shrimps were fed with newly hatched Artemia nauplii as a satiation feed three times daily (08.00 a.m., 01.00 p.m. and 06.00 p.m.). Fecal matter and uneaten feed in tanks were siphoned every day.

After one week of acclimation, 1800 shrimps of similar size (average initial weight of 27.25 ± 6.54 mg and length of 20.90 ± 2.06 mm) were randomly distributed into a closed recirculating aquaculture system equipped with twelve 100 m3 fiberglass tanks containing 70 m3 of seawater salinity 25 ppt (Figure 1). Each fiberglass tank contained 150 shrimps with three replicate tanks per experimental treatments. Four different types of feeds i.e., newly hatched Artemia (Ar), rotifer Brachionus rotundiformis (Ro), newly hatched Artemia + rotifer (ArRo) and shrimp larvae commercial feed (SF) were applied to treatments I, II, III and IV respectively. The particle size of SF was 250 - 500 µ with nutritional profile as shown in Table 1 (Lansy-Shrimp PL (INVE®, Phichit, Thailand). Shrimps were fed daily ad libitum three times a day (08.00 a.m., 01.00 p.m. and 06.00 p.m.) with four different feeds. The experimental time lasted 70 days (10 weeks).

2.2. Water Quality

Water quality including temperature, salinity, dissolved oxygen, pH, alkaline,

Figure 1. Diagram showing a closed recirculating aquaculture system equipped with twelve 100 m3 fiberglass tanks (T = treatment, R = replicate), (T1 = Ar, T2 = Ro, T3 = ArRo, T4 = SF).

Table 1. Nutritional profile of the shrimp larvae commercial feed (SF) according to manufactures (Lansy-Shrimp PL (INVE®, Phichit, Thailand).

ammonia, nitrite and nitrate of each treatment was controlled right weekly before and during the cultivated period. Temperature, salinity and dissolved oxygen were determined directly by digital water analysis instrument (Multi-probe, YSI Pro 2010); while pH was measured using pH meter (Horiba Model: pH-22). Alkalinity was measured titrimetrically; while Nitrite was measured using spectrophotometer (Thermo Scientific, Genesys 20).

2.3. Data Collection and Calculation

Twenty individual shrimps were randomly collected to determine growth performance parameters immediately before being arranged in the tanks and every fortnight during the experimental period. At each sampling, each organism was gently blotted dry and weighed individually using four digital balances Sartorius, AX224). Simultaneously the length was measured from the rostrum tip to the telson end using a digital vernier caliper.

At the end of experiment, the total number, weight and length of shrimps in each experimental tank were determined. The daily weight gains, daily length gains, specific growth rate (body weight), specific growth rate (body length) and the survival rates were calculated using the following equations [22] :

Weight gain (WG) (mg) = Final weight (mg) − Initial weight (mg)

Length gain (LG) (mm) = Final length (mm) − Initial length (mm)

Daily weight gain (mg day1) = (Final weight − Initial weight)/Culturing days

Daily length gain (mm day1) = (Final length − Initial length)/Culturing days

Specificgrowthrate = ( Lnfinalweight Lninitialweight ) Culturingdays × 100 (body weight) (% day1)

Specific growth rate = ( Ln final length Ln initial length ) Culturing days × 100 (body length) (% day1)

Survivalrate ( % ) = Final shrimp number Initial shrimp number × 100

2.4. Statistical Analysis

One-way analysis of variance (ANOVA) was conducted on all data, followed by Tukey’s multiple range tests to identified significant differences between the mean values (significance level of p ≤ 0.05) using the Statistical Package for the Social Science (SPSS) software for Windows version 19.0.

3. Results and Discussion

3.1. Water Quality

Water quality in each experimental tank deteriorated due to the accumulation of fecal matter and the decomposition of uneaten food. Thus, a daily water change of 30% of the total water volume had been done. Changing water was done by using a siphon with a strainer at the intake end. Regular siphoning of sediments at the bottom of culture tanks was done 3 times a week.

The values of water quality parameters, including temperature, salinity, dissolved oxygen, pH, alkaline, ammonia, nitrite, and nitrate are presented in Table 2. All water quality parameters in all experimental tanks fluctuated within the suitable range for the whole period of culture and were within the optimal range for shrimp culture [23] [24] .

3.2. Body Weight Gains

Data in Figure 2 show that the mean weight of A. vulgaris increased with culturing time in all treatments. After 70 days, the mean weight of shrimps increased from the initial weight (27.25 ± 6.54 mg) to 70.37 ± 18.41, 54.37 ± 16.03, 69.49 ± 24.94 and 61.58 ± 18.82 mg in treatment feed with Artemia (Ar), Rotifer (Ro), Artemia + Rotifer (ArRo) and Shrimp larvae commercial feed (SF) respectively.

The mean final weight of shrimps ranged between 54.37 ± 16.03 mg to 70.37 ± 18.41 mg, with the highest in Ar treatment and lowest in Ro treatment. Shrimps reared with Ro had the lowest weight and were not significantly different with treatment feed with SF (p ≥ 0.05) but significantly different with treatment feed with Ar, and ArRo (p ≤ 0.05). The mean final weight of shrimps reared with SF was not significantly different with treatment feed with Ar, ArRo and Ro (p ≥ 0.05).

Table 2. Mean water quality parameters analyzed in different feeds treatments during 70 days of rearing A. vulgaris.

Figure 2. Mean weight of A. vulgaris in different feeds during periods of culture. Artemia (Ar), Rotifer (Ro), Artemia + Rotifer (ArRo) and Shrimp larvae commercial feed (SF).

Similar results were found for the weight gains, daily weight gains and specific growth rate that shrimps reared with Ro had the lowest weight gain and daily weight gain and were not significantly different with treatment feed with SF (p ≥ 0.05) but significantly different with treatment feed with Ar and ArRo (p ≤ 0.05). The weight gains daily weight gain and specific growth rate of shrimps reared with SF were not significantly different with treatment feed with Ar, ArRo and Ro (p ≥ 0.05). (Table 3)

3.3. Body Length Gains

Data in Figure 3 show that the mean length of A. vulgaris increased with culturing time in all treatments. After 70 days, the mean length of shrimps increased from the initial length (20.90 ± 2.06 mm) to 27.49 ± 2.13, 26.41 ± 2.72, 27.90 ± 4.34 and 27.01 ± 2.92 mm in treatment feed with Artemia (Ar), Rotifer (Ro), Artemia + Rotifer (ArRo) and Shrimp larvae commercial feed (SF) respectively.

The mean final length of shrimps ranged between 26.41 ± 2.72 mm to 27.90 ± 4.34 mm, with the highest in ArRo treatment and lowest in Ro treatment. Shrimps reared with Rotifer (Ro) had the lowest length and were significantly different with treatment feed with Ar, ArRo and SF (p ≤ 0.05). The mean final length of shrimps reared with SF was not significantly different with treatment feed with Ar and ArRo (p ≥ 0.05).

Similar results were found for the length gains, daily length gains and specific growth rate (body length) that shrimps reared with Ro had the lowest length gain, daily length gain and specific growth rate (body length) and were significantly different with treatment feed with Ar, ArRo and SF (p ≤ 0.05). The length gains and daily length gain and specific growth rate (body length) of shrimps reared with SF were not significantly different with treatment feed with Ar, ArRo and Ro (p ≥ 0.05) (Table 4).

Table 3. Mean initial weight, final weight, weight gain, daily weight gain and specific growth rate (body weight) of A. vulgaris reared with different feeds within 70 days.

Values are presented as mean ± SD of three replicates. Different superscripts in the same column show significant difference (p ≤ 0.05).

Table 4. Effect of different food on the final weight, weight grain, daily weight gain, daily length grain, specific growth rate and survival rate of Acetes vulgaris during 70 days rearing.

Values are presented as mean ± SD of three replicates. Different superscripts in the same column show significant difference (p ≤ 0.05).

Figure 3. Mean length of A. vulgaris in different feeds during periods of culture. Artemia (Ar), Rotifer (Ro), Artemia + Rotifer (ArRo) and Shrimp larvae commercial feed (SF).

3.4. Survival Rates

The survival rate of A. vulgaris after 70 days of culture with different feeds ranged from 75.78 ± 3.36 to 81.78 ± 3.08, with the highest value in SF treatment and the lowest value in Ro treatment (Table 5). The survival rate of shrimp in SF treatment was significantly different with treatment feed with Ar, Ro and ArRo

Table 5. Mean survival rates (%) of A. vulgaris cultured in different foods for 70 days rearing.

Values are presented as mean ± SD of three replicates. Different superscripts in the same column show significant difference (p ≤ 0.05).

(p ≤ 0.05). But the differences were not significant among the Ar, Ro and ArRo treatments (p ≥ 0.05).

[25] reported effects of different food on survival of A. sibogae australis by comparing feeding shrimp with natural detritus and newly hatched Artemia and found that specimens fed natural detritus lived shorter (3 - 17 days) than those fed Artemia nauplii (11 - 64 days). Artemia is a beneficial to the growth and survival rated of pelagic shrimp (Neomysis intermedia, Metamysidopsis elongate, Lucifer chacei, Sergia lucens and Sergestes similis) and it is also an important feed for the caridean shrimp (Palaemon serratus) [25] . The effect of different food on growth and survival rate of A. vulgaris in this study also revealed that Acetes shrimps has ability to eat a variety of foods and can eat food of various sizes since they can eat rotifer, Artemia and shrimp larvae commercial feed.

Specific growth rates (both for body weight and body length) of shrimps reared with SF were not significantly different with treatment feed with Ar, ArRo and Ro (p ≥ 0.05). This is postulated that Acetes shrimps can eat both live feeds and formulated feeds and being an omnivore species. This is likely to [26] studied food and feeding habit of Taiwan mauxia shrimp Acetes intermedius in the coastal waters of Southwestern Taiwan and concluded that Acetes is an omnivore species, feeding on a wide range of food items [12] . In their natural habitat, they eat several things like phytoplankton, zooplankton, algae, plant matter, debris, sand and mud [13] [14] [15] [16] .

Typically, larvae stages of marine species are fed live feeds such as algae, zooplankton, rotifers and Artemia. In this study, rotifer and Artemia were used as live feed as well as pellet feed. The nutritional composition of different feeds used in this experiment was found to have different nutritional values. Newly hatched Artemia contain 57.26% protein, 16.21% fat and 6.67% carbohydrate) [27] (Brachionus rotifer contains 59.0% protein, 13.0% fat and 3.1% highly unsaturated fatty acid) [28] (Shrimp larvae commercial feed used in this study contains 48.0% protein, 9.0% fat, 2.5% ash and 9% moisture (Lansy-Shrimp PL (INVE®, Phichit, Thailand). Although live feeds provide an excellent source of nutrition, several limitations are associated with their use. Rotifers require considerable expenditures in time and effort to maintain, and live artemia nauplii suffer from inconsistent supply [29] . Thus, shrimp larvae commercial feed is probably the most benefit convenience for a commercial culture of Acetes species in the future.

4. Conclusion

The sergestid shrimp Acetes vulgaris has ability to consume both live feeds and pellet feed. SF gave the highest survival rates (p ≤ 0.05) and the specific growth rates were not significantly different with treatment feed with Ar, ArRo and Ro (p ≥ 0.05) The findings reflected the ability of Acetes shrimps to consume divers food types including both live feed and pelleted feed. Insights obtained from this research suggested that artificial feed can be as efficient as live feeds. This new knowledge is a needed addition to a currently lacking knowledge base for aquaculture of this Acetes species.

Acknowledgements

We would like to thank the Biodiversity-based economy development office (BEDO) (grant number 3/2562) for supporting this research project.

Conflicts of Interest

The authors declare no conflicts of interest regarding the publication of this paper.

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