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Research article · 2025 · Full text

International Journal of Agriculture and Food Science

Effect of ginger (Zingiber officinale) rhizome extract on growth performance, survival and gut flora of common carp (Cyprinus carpio)

R. S. BhandariKanti ShresthaDhundy R. Bastola

Volume 7(4) · Pages 111–115 · DOI: 10.33545/2664844x.2025.v7.i4b.343 ↗

Research areasGinger and Zingiberaceae researchAquaculture disease management and microbiotaAquatic life and conservation

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Abstract

Author-written

Phytogenics, or plant-based additives, are pivotal for growth enhancement and disease resistance in cultured fish diets. A 60-days feeding trial was carried out in hapas (1m×1m×1.2m) within a grow tank (5 m×5 m×1.5 m) at the Department of Aquaculture, Agriculture hatchery complex. The study aimed to assess growth performance, survival, and gut flora of Cyprinus carpio fed with varying levels of Zingiber officinale rhizome extract. An initial cohort comprising 450 juveniles (fry) of C. carpio, averaging 2.55±0.03 g in weight and 4.9±0.68cm in length, were fed with diets containing 27.15% crude protein, included four concentrations of Z. officinale rhizome extract (1%, 2%, 3%, and 4%), along with a control group (0%); feeding three times a day for a total of 60 days, with each meal amounting to 5% of their body weight. Fish group receiving the diet containing 3% Ginger rhizome extract, showed the highest values for growth performance parameters (p

Summary

Source-checked

Plain-language reading of the full paper, prepared with AI and checked against the text. Each point links to the authors' own words.

  1. Why it matters

    • Plant-based additives, known as phytogenics, are important for improving the growth and disease resistance of fish in aquaculture. View evidence ↗

      Why it matters

      Plant-based additives, known as phytogenics, are important for improving the growth and disease resistance of fish in aquaculture.

      In the paper's own words

      “Phytogenics, or plant-based additives, are pivotal for growth enhancement and disease resistance in cultured fish diets.”

      Page 1

      Found in: Introduction

      Read it in the full textOpen PDF at page 1 ↗
    • Due to concerns over environmental impact and antibiotic resistance, researchers are shifting toward dietary supplements to manage stress and disease in intensive aquaculture. View evidence ↗

      Why it matters

      Due to concerns over environmental impact and antibiotic resistance, researchers are shifting toward dietary supplements to manage stress and disease in intensive aquaculture.

      In the paper's own words

      “Intensified aquaculture can lead to water quality decline, stress, and disease (Hoseinifar, Soleimani, & Ringø, 2014) [10] while antibiotics and chemicals were traditionally used to mitigate these issues (Mohammadi et al., 2020) [13]. Concerns over resistance and environmental impact have shifted focus towards dietary supplements for improved fish health”

      Page 1

      Found in: Introduction

      Read it in the full textOpen PDF at page 1 ↗
    • Common carp (Cyprinus carpio) are a preferred species for farming because they adapt well and grow quickly. View evidence ↗

      Why it matters

      Common carp (Cyprinus carpio) are a preferred species for farming because they adapt well and grow quickly.

      In the paper's own words

      “Common carp (Cyprinus carpio) are favored for their rapid growth and adaptability (Tokur et al., 2006) [12].”

      Page 1

      Found in: Introduction

      Read it in the full textOpen PDF at page 1 ↗
  2. The question

    • The study aimed to evaluate how different concentrations of ginger (Zingiber officinale) rhizome extract affect the growth, survival, and gut bacteria of common carp. View evidence ↗

      The question

      The study aimed to evaluate how different concentrations of ginger (Zingiber officinale) rhizome extract affect the growth, survival, and gut bacteria of common carp.

      In the paper's own words

      “The study aimed to assess growth performance, survival, and gut flora of Cyprinus carpio fed with varying levels of Zingiber officinale rhizome extract.”

      Page 1

      Found in: Discussion

      Read it in the full textOpen PDF at page 1 ↗
  3. What they did

    • The experiment used 450 common carp fry (avg. 2.55±0.03 g) fed a 27.15% crude protein diet with ginger extract levels of 0%, 1%, 2%, 3%, and 4% for 60 days. View evidence ↗

      What they did

      The experiment used 450 common carp fry (avg. 2.55±0.03 g) fed a 27.15% crude protein diet with ginger extract levels of 0%, 1%, 2%, 3%, and 4% for 60 days.

      In the paper's own words

      “An initial cohort comprising 450 juveniles (fry) of C. carpio, averaging 2.55±0.03 g in weight and 4.9±0.68cm in length, were fed with diets containing 27.15% crude protein, included four concentrations of Z. officinale rhizome extract (1%, 2%, 3%, and 4%), along with a control group (0%); feeding three times a day for a total of 60 days, with each meal amounting to 5% of their body weight.”

      Page 1

      Found in: Discussion

      Read it in the full textOpen PDF at page 1 ↗
    • The study employed a Complete Randomized Design using nylon hapas in cemented tanks, with 30 fry per hapa and three replicates per treatment. View evidence ↗

      What they did

      The study employed a Complete Randomized Design using nylon hapas in cemented tanks, with 30 fry per hapa and three replicates per treatment.

      In the paper's own words

      “A Complete Randomized Design (CRD) was used. 1 m x 1 m x 1.2 m nylon hapas were placed in 5 m x 5 m x 1.5 m cemented tanks. Treatments were randomly assigned to three tanks each via lottery. Each hapas contains 30 fries.”

      Page 2

      Found in: Experimental setup

      Read it in the full textOpen PDF at page 2 ↗
    • Gut flora was analyzed by counting aerobic heterotrophic bacteria from gut suspension samples using nutrient agar plates, with results reported in cfu/ml. View evidence ↗

      What they did

      Gut flora was analyzed by counting aerobic heterotrophic bacteria from gut suspension samples using nutrient agar plates, with results reported in cfu/ml.

      In the paper's own words

      “A 1 ml gut suspension sample was serially diluted to 10⁻⁹. 0.1 ml aliquots were spread onto nutrient agar plates in triplicate and incubated at 37 °C for 48 hours. Aerobic heterotrophic bacteria were counted, and results were expressed as cfu/ml.”

      Page 3

      Found in: Total aerobic heterotrophic plate count

      Read it in the full textOpen PDF at page 3 ↗
  4. What they found

    • Carp fed a 3% ginger extract diet achieved the best growth results, including a harvesting weight of 10.33±1.32 g/fish and a specific growth rate of 2.33±0.18%/day, significantly outperforming the control group. View evidence ↗

      What they found

      Carp fed a 3% ginger extract diet achieved the best growth results, including a harvesting weight of 10.33±1.32 g/fish and a specific growth rate of 2.33±0.18%/day, significantly outperforming the control group.

      In the paper's own words

      “Fish group receiving the diet containing 3% Ginger rhizome extract, showed the highest values for growth performance parameters (p<0.05), including average harvesting weight (10.33±1.32 g/fish), total harvesting weight (247.82±31.60 g/hapa), daily weight gain (0.13±0.01g/fish/day), specific growth rate (2.33±0.18%/ day) in comparison with control group.”

      Page 1

      Found in: Discussion

      Read it in the full textOpen PDF at page 1 ↗
    • The 3% ginger extract diet most effectively reduced gut bacterial load, reaching 1.62×106±3.60×104 cfu/ml by day 60. View evidence ↗

      What they found

      The 3% ginger extract diet most effectively reduced gut bacterial load, reaching 1.62×106±3.60×104 cfu/ml by day 60.

      In the paper's own words

      “The least total bacterial count was recorded in group fed 3% ginger rhizome extract on observation at 20 days (1.75×108±2.64×106 cfu/ml), 40 days (1.9×107±4.23×106 cfu/ml), and 60 days (1.62×106±3.60×104 cfu/ml).”

      Page 1

      Found in: Discussion

      Read it in the full textOpen PDF at page 1 ↗
    • Varying the levels of ginger extract in the diet did not significantly alter water quality parameters. View evidence ↗

      What they found

      Varying the levels of ginger extract in the diet did not significantly alter water quality parameters.

      In the paper's own words

      “Similarly, the effects of varying level of ginger rhizome extract on the water quality parameters were not significantly different (p>0.05).”

      Page 1

      Found in: Discussion

      Read it in the full textOpen PDF at page 1 ↗
  5. What it means

    • The authors conclude that a 3% ginger extract diet is an effective natural alternative to antibiotics for improving growth, survival, and gut health in common carp fry. View evidence ↗

      What it means

      The authors conclude that a 3% ginger extract diet is an effective natural alternative to antibiotics for improving growth, survival, and gut health in common carp fry.

      In the paper's own words

      “This study demonstrated that a 3% ginger extract diet significantly improved common carp fry growth, survival, and reduced gut bacteria, offering a natural alternative to antibiotics.”

      Page 5

      Found in: Conclusion

      Read it in the full textOpen PDF at page 5 ↗

Visual summary

2 visuals

Illustrations explain the paper; charts are replotted from the paper's own table values.

AI-generated illustration
AI-generated conceptual illustration (common carp (Cyprinus carpio)). It explains the idea and does not show study data.↗ Enlarge
Effect of Ginger Extract on Carp
AI-generated conceptual illustration (common carp (Cyprinus carpio)). It explains the idea and does not show study data.

AI-generated conceptual illustration (common carp (Cyprinus carpio)). It explains the idea and does not show study data.

Open full-size image ↗

Effect of Ginger Extract on Carp

AI-generated conceptual illustration (common carp (Cyprinus carpio)). It explains the idea and does not show study data.

View source evidence ↗
Replotted from source data
Replotted from Table 2 (page 3) of the original paper. Every bar is the paper's own table value.↗ Enlarge
T1 and T2 and more: Average harvesting... vs Specific growth rate...
Replotted from Table 2 (page 3) of the original paper. Every bar is the paper's own table value.

Replotted from Table 2 (page 3) of the original paper. Every bar is the paper's own table value.

Open full-size image ↗

T1 and T2 and more: Average harvesting... vs Specific growth rate...

Replotted from Table 2 (page 3) of the original paper. Every bar is the paper's own table value.

View source evidence ↗

Figures & tables

From the original paper
Treatment design with ratio of Ginger rhizome extract in experimental feed.Table 1Page 2% CP and % DM of feed ingredients used in experiment.Table 1Page 2Proximate composition of experimental dietTable 3Page 3Effect of varying levels of ginger rhizome extract on growth performance of Common carp fry (Mean±SEM)Table 2Page 3Graphical presentation of average weight gain (g/fish) of fish during treatment periodFigure 2Page 3Effect of varying levels of Ginger rhizome extract on gut flora (TBC) count of Common carp fry (Mean±SEM)Table 5Page 4Weekly averages dissolve oxygen concentration (mg/L) during experimental period.Figure 3Page 4Weekly average pH of water during the experimental period.Figure 4Page 4Weekly average temperature (°C) during experimental period.Figure 5Page 4
FULL TEXT Original article · reflowed for reading

Introduction

The aquaculture and fisheries sectors in Nepal are pivotal contributors to national food security, economic output, and employment contributing 17% of global human consumption of animal protein. Nepal's annual fish production amounts to 104,623 mt. of which 21,000 mt. are derived from capture fisheries, while aquaculture contributes 73,693 mt. accounting for 0.44% of the GDP and 1.44% of the Agricultural Gross Domestic Production (AGDP) (CFPCC, 2022) [1] . Intensified aquaculture can lead to water quality decline, stress, and disease (Hoseinifar, Soleimani, & Ringø, 2014) [10] while antibiotics and chemicals were traditionally used to mitigate these issues (Mohammadi et al., 2020) [13] . Concerns over resistance and environmental impact have shifted focus towards dietary supplements for improved fish health, particularly in larval and fry stages (Hoseinifar, Soleimani, & Ringø, 2014) [10] . Herbal plants, with medicinal properties, offer potential for enhancing fish health and growth in aquaculture (Gabriel, 2021). Research indicates various plant parts improve growth, antioxidant profiles, immunity, and survival in farmed fish (Jafarinejad et al., 2020) [11] . Common carp (Cyprinus carpio) are favored for their rapid growth and adaptability (Tokur et al., 2006) [12] . However, plant-based feeds, while desirable, contain anti-nutritional factors (ANFs) that can negatively impact gut microbes, digestibility, growth, immunity, and disease resistance in carp (Apines-Amar et al., 2016) [26] . Ginger (Zingiber officinale), used medicinally and as a supplement (Jafarinejad et al., 2020 [11] , contains carbohydrates, protein, lipids, fiber, proteases, and volatile compounds like [3] . Ginger powder has shown positive effects on fish growth, hematology, immunity, and antioxidant profiles ( [14,15,3] . It also enhances digestion and regulates gut bacteria by stimulating pancreatic enzyme and bile secretion (Baliga et al., 2011) [16] . Gastro-intestinal tract (GIT) microorganisms improve digestion through enzyme provision and vitamin synthesis (Tovar-Ramírez et al., 2004) [25] , with their composition heavily influenced by diet (Nayak, 2010) [24] . Adegbesan et al. (2019) [2] showed ginger reduces gut bacterial and fungal counts in Clarias gariepinus (p<0.05). A 2% ginger diet resulted in the lowest counts (7.4×10 5 bacteria, 2.0×10 5 fungi), followed by a 3% diet. Abbasi Ghadikolaei et al. (2017) [8] found that 2% dietary ginger powder significantly improved growth and biochemical composition in juvenile common carp. Adegbesan et al. (2019) [2] found Streptococcus agalactiae, Bacillus subtilis, and Enterococcus faecalis in Clarias gariepinus intestines fed ginger, suggesting increased grampositive bacteria. This aligns with findings by Olojo et al.

(2010) [17] and Nwabueze (2014) [19] regarding similar bacterial flora in C. gariepinus. Similarly, M Alsaiad, S., & M AL-Zayat, (2019) [18] found ginger increased feed costs, but improved weight gain. However, the impact of ginger on gut flora requires further study. This research aims to assess ginger's effects on common carp growth, survival, and gut flora.

Materials and Methods

Materials and Methods

Site Selection

The research was conducted at the Hatchery Complex within the Fisheries Program of Agriculture and Forestry University, spanning from June to August 2022. The site was located at 27°39'26.5"N longitude & 84°20'58.6"E latitude.

Experimental Setup Experimental fish

Fries of Common Carp with average individual weight of 2.55±0.03 g and length 4.9±0.68 cm were procured from CAARP, Kathar, Chitwan (Private farm) which were kept in conditioning for 30 minutes prior to transferring them on holding tank.

Treatment design

A 60-day feeding trial, with three replicates per treatment, tested various ginger rhizome extract ratios across five treatment groups (Table 1).

Table 1. % CP and % DM of feed ingredients used in experiment.
SNFeed ingredientsProximate composition—
CP %DM %
1Rice bran13.790.8
2Corn flour12.489.9
3Mustard oil cake32.595.8
4Soyabean meal47.0993

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% CP and % DM of feed ingredients used in experiment.↗ Enlarge
Table 1
% CP and % DM of feed ingredients used in experiment.

% CP and % DM of feed ingredients used in experiment.

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Original paper tableSource PDF · page 2 ↗
Table 1. Treatment design with ratio of Ginger rhizome extract in experimental feed.
Treatment No.TreatmentRatio of Ginger rhizome extract (%)
T1Control0
T2Pellet feed + Ginger rhizome extract1
T3Pellet feed + Ginger rhizome extract2
T4Pellet feed + Ginger rhizome extract3
T5Pellet feed + Ginger rhizome extract4

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Treatment design with ratio of Ginger rhizome extract in experimental feed.↗ Enlarge
Table 1
Treatment design with ratio of Ginger rhizome extract in experimental feed.

Treatment design with ratio of Ginger rhizome extract in experimental feed.

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Original paper tableSource PDF · page 2 ↗

Tank preparation and hapas installation

Cement tanks were drained, fish and debris removed, and air-dried. Tanks were disinfected with 2 g/1000L KMnO 4 , dried again, and refilled to 1.2 m. Nylon hapas, disinfected with 5% salt, were secured in tanks with bamboo and iron supports. Natural algal blooms eliminated the need for fertilization.

Experimental setup

A Complete Randomized Design (CRD) was used. 1 m x 1 m x 1.2 m nylon hapas were placed in 5 m x 5 m x 1.5 m cemented tanks. Treatments were randomly assigned to three tanks each via lottery. Each hapas contains 30 fries.

Experimental feed Proximate composition

To prepare the experimental feed of CP (27.15%) the ingredients used are mentioned in Table 2.

Table 2. Effect of varying levels of ginger rhizome extract on growth performance of Common carp fry (Mean±SEM)
ParametersT1T2T3T4T5
Average stocking weight (g/fish)2.55±0.04a2.55±0.03a2.56±0.03a2.53±0.03a2.55±0.03a
Average harvesting weight (g/fish)5.76±0.13c5.83±0.09c7.39±0.90b10.33±1.32a9.61±1.16a
Harvested number (Nos.)22±0.57b23±0.00ab24±0.00a24±0.00a24±0.00a
Total harvesting weight (g/hapa)138.28±3.13c141.16±4.37c177.48±2.11b247.82±31.60a230.63±28.12a
Daily weight gain (g/fish/day)0.053±0.005c0.053±0.005c0.08±0.00b0.13±0.01a0.11±0.01a
Specific growth rate (%/day)1.35±0.06c1.38±0.04c1.76±0.03b2.33±0.18a2.20±0.22a
Survival rate (%)93.05±1.39 c95.83±0.00 b100±0.00 a100±0.00 a100±0.00 a

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Effect of varying levels of ginger rhizome extract on growth performance of Common carp fry (Mean±SEM)↗ Enlarge
Table 2
Effect of varying levels of ginger rhizome extract on growth performance of Common carp fry (Mean±SEM)

Effect of varying levels of ginger rhizome extract on growth performance of Common carp fry (Mean±SEM)

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Original paper tableSource PDF · page 3 ↗

Preparation of ginger rhizome extract

Local ginger rhizomes were washed, peeled, and sliced before being dried at 40 °C for 72 hours. The dried slices were then ground, sieved, and 20 g of the resulting powder was macerated in 100ml of 35 °C distilled water for 48 hours. Following maceration, the extract was filtered, dried at 40 °C for another 72 hours, cooled to room temperature, and finally stored at 4 °C.

Experimental diet and feeding

A 27.15% CP pellet feed was formulated from crushed ingredients suitable for carp fry. Extracts, prepared according to treatment, were dissolved in 90% ethanol, sprayed onto the feed, and mixed thoroughly. The experimental diet was then air-dried for 3 hours and stored. Juvenile common carp were fed this diet three times daily at 5% of their body weight for 60 days.

Data collection

Fish growth was measured before and after treatment. Gut bacteria counts were taken from two fish per group every 20 days. Fish used for bacteria counts were excluded from growth performance measurements.

Growth parameters and Survival

Daily weight gain (g fish day ⁄ ⁄ ) = Mean final weight (g) -Mean initial weight(g) Where, Nf= final number of fish stock, Ni= Initial number of fish stock.

Examination of Gut flora Collection of intestines

Fish were washed, disinfected with 90% ethanol, and anesthetized with 0.1 ml/L clove oil for 30 minutes. Under aseptic conditions, the gut was removed, homogenized, and 2 g of the homogenate was suspended in 25 ml normal saline (NS) to create a stock solution, stored at 4 °C.

Total aerobic heterotrophic plate count

A 1 ml gut suspension sample was serially diluted to 10⁻⁹. 0.1 ml aliquots were spread onto nutrient agar plates in triplicate and incubated at 37 °C for 48 hours. Aerobic heterotrophic bacteria were counted, and results were expressed as cfu/ml.

Water quality analysis

Maintaining good water quality is of utmost importance for promoting growth and preventing diseases. The parameters of water quality, including Dissolved oxygen (DO), pH, and Temperature, were assessed on a daily basis

Proximate analysis

Random sampling was carried out for each batch of feed produced throughout the experiment. These samples, which represented the diets, were subjected to proximate analysis following the guidelines outlined in AOAC (2000) [4] . The analysis was conducted at the Animal Nutrition Laboratory of Agriculture and Forestry University in Rampur, Chitwan, Nepal.

Statistical analysis

Statistical analysis was conducted using R (version 3.6.1). ANOVA was used to assess treatment mean variations, with significance set at p< 0.05. Mean values are presented with their standard error of the mean (± SEM).

Result Proximate composition of diet

Result Proximate composition of diet

Microbial count

Microbial count

Water quality analysis

Water quality analysis

Discussion

The water conditions, including temperature, dissolved oxygen levels, and pH, were maintained within the optimal range for Common carp culture, consistent with the research carried out by Nasir and Khalil in 2016 [20] and the guidelines from NSA (1999). Among the treatments, T 4 (3% Ginger rhizome extract) recorded the higher value of parameters followed by T 4 (4% Ginger rhizome extract) depicting the growth performance of Common carp fry. Adegbesan et al. (2019) [2] reported that fish (Clarias gariepinus) exhibited a consistent rise in weight gain, with the most substantial growth performance observed in those fed diets containing 1% and 3% Ginger rhizome powder.

Likewise, in a research study conducted by Jafarinejad, Gharaei, and Mirdar (2020) [11] , they investigated the impact of a ginger-infused diet on the growth characteristics of Cyprinus carpio. Their findings indicated that fish that were fed diets containing 2% to 5% ginger experienced a substantial rise in final weight, weight gain, specific growth rate, and improved feed conversion ratio (FCR) compared to the fish on the control diet. These findings align with the results of the present study, suggesting that the level of ginger inclusion in the diet plays a crucial role in promoting higher growth rates in Cyprinus carpio. The findings of present study on growth performance of C. carpio are congruent with Makode (2017) [22] who found similar report after incorporation of onion powder @ 3% had yield the higher growth performance. Similar results were also reported by Gabor et al. (2010) [6] and Gabor et al. (2012) [7] . Rawat et al. (2022) [23] reported the growth-promoting effects of ginger in the diet can be attributed to improved nutrient digestibility and enhanced digestion and absorption of protein components which is in line with study conducted by Talpur et al., (2013) [14] and Hassanin et al. (2014) [9] . Significant distinctions (p< 0.05) were noted in the reduction of the total bacterial count among fish fed different concentrations of Zingiber officinale extract, with the lowest bacterial count observed in fish that consumed a diet containing 3% Ginger rhizome extract, as compared to the control group. This result aligns with the research conducted by Adegbesan et al. (2019) [2] , where the lowest bacterial count was found in the group fed with 2% ginger root powder (7.4±5.31×10 5 cfu/ml), followed by 3% ginger powder (8.84±7.58 ×10 5 cfu/ml). Similarly, Bello et al.

(2012) [5] reported a decline in bacterial load in groups supplemented with onion bulb and walnut leaves, with increasing levels of inclusion and over time.

Conclusion

Aquaculture intensification necessitates sustainable strategies to combat disease and stress. This study demonstrated that a 3% ginger extract diet significantly improved common carp fry growth, survival, and reduced gut bacteria, offering a natural alternative to antibiotics.

Acknowledgement

AcknowledgementThe authors gratefully acknowledge Agriculture and Forestry University for their invaluable technical and financial contributions to this research. Furthermore, sincere appreciation is extended to all individuals whose collaborative efforts facilitated the successful completion of this study.

Figures and tables from the paper

Table 3. Proximate composition of experimental diet
SNProximate compositionPercentage (%)
1Moisture11.2
2Crude protein27.15
3Crude fat5.75
4Crude fiber4.00
5Total ash5.80
6Metabolic energy3239.63Kcal/kg

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Table 3
Proximate composition of experimental diet

Proximate composition of experimental diet

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Figure 2. Graphical presentation of average weight gain (g/fish) of fish during treatment period
Graphical presentation of average weight gain (g/fish) of fish during treatment period↗ Enlarge
Figure 2
Graphical presentation of average weight gain (g/fish) of fish during treatment period

Graphical presentation of average weight gain (g/fish) of fish during treatment period

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Table 5. Effect of varying levels of Ginger rhizome extract on gut flora (TBC) count of Common carp fry (Mean±SEM)
TreatmentBacterial count (cfu/ml)———
Initial20DAT40DAT60DAT
T11.38×1092.14 ×108 ±6.55×106 bc2.9×108 ±2.78×107 a2.71×109 ±1.62×108 a
T21.38×1093.31×108±3.91×107 a3.1×108 ±5.89×107 a1.88×108 ±9.50×107 b
T31.38×1092.24×108±1.83×107 b2.2×107 ±4.36×106 b6.30×106 ±7.88×106 c
T41.38×1091.75×108±2.64×106 c1.9×107 ±4.23×106 b1.62×106 ±3.60×104 c
T51.38×1092.06×108±2.26×107 bc2.2×107 ±2.87×106 b1.99×106 ±1.68×105 c

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Table 5
Effect of varying levels of Ginger rhizome extract on gut flora (TBC) count of Common carp fry (Mean±SEM)

Effect of varying levels of Ginger rhizome extract on gut flora (TBC) count of Common carp fry (Mean±SEM)

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Original paper tableSource PDF · page 4 ↗
Figure 3. Weekly averages dissolve oxygen concentration (mg/L) during experimental period.
Weekly averages dissolve oxygen concentration (mg/L) during experimental period.↗ Enlarge
Figure 3
Weekly averages dissolve oxygen concentration (mg/L) during experimental period.

Weekly averages dissolve oxygen concentration (mg/L) during experimental period.

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Figure 4. Weekly average pH of water during the experimental period.
Weekly average pH of water during the experimental period.↗ Enlarge
Figure 4
Weekly average pH of water during the experimental period.

Weekly average pH of water during the experimental period.

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Figure 5. Weekly average temperature (°C) during experimental period.
Weekly average temperature (°C) during experimental period.↗ Enlarge
Figure 5
Weekly average temperature (°C) during experimental period.

Weekly average temperature (°C) during experimental period.

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References

23 in the original paper
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