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The Biochemical Composition and Quality of Adult Chinese Mitten Crab Eriocheir sinensis Reared in Carbonate Alkalinity Water

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04 January 2024

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Abstract
Saline-alkaline aquaculture has become important breakthrough to expand available space for aquaculture in China. However, the biochemical composition and quality of Eriocheir sinensis reared in carbonate alkalinity water are still unclear. Therefore, this study investigated the edible yield, coloration, nutritional and flavor quality of Eriocheir sinensis. Significantly lower gona-dosomatic index (GSI) and meat yield (MY) were detected in intensive pond (IP) than those in semi intensive reed wetland (SIWR) (P< 0.05). Six color parameters differed between IP and SIRW in the hepatopancreas (P< 0.05). The contents of crude protein and fat in the female hepatopan-creas of IP were significantly higher than those in SIRW(P< 0.05). The higher concentrations of ∑MUFA, ∑EFA, h/H in the female edible tissues were checked in IP than those in SIRW, with significant difference including ∑MUFA in the hepatopancreas and ovary, ∑EFA in the muscle, and h/H in the ovary (P<0.05). Better total free amino acid (∑FAA) contents of muscle were de-tected in SIRW than that in IP. Significantly increasing tendency was detected in K, Ca, Mg, Fe, Zn of ovary from SIRW to IP (P< 0.05). Overall, the Eriocheir sinensis reared in carbonate alkalinity water is an important source of nutrient.
Keywords: 
Subject: Biology and Life Sciences  -   Food Science and Technology

1. Introduction

Saline-alkaline land, accounting for 0.95 billion ha, covers approximately 7.26% of the total land area worldwide [1], of which 99.13 million ha saline-alkaline land are located in China including approximately 45.87 million ha of low-lying saline-alkaline water mainly distributed in northeast, northwest, and coastal areas [2]. Salinity and carbonate alkalinity, serving as the most significant stressors in saline-alkaline water, have a substantial impact on the aquatic animals of growth, survival, reproduction, and quality [3,4,5]. Physiological metabolism, osmoregulation and intestinal microbiota of aquatic animals can be significantly influenced by high saline-alkaline concentrations [6,7,8,9,10,11,12]. Therefore, not all the aquatic animals can be reared in the saline-alkaline water. Only a few species, such as Nile tilapia Oreochromis niloticus [9], crucian carp Carassius auratus [10], Chinese mitten crab Eriocheir sinensis [11], naked carp Gymnocypris przewalskii [12], Bulatmai barbel Luciobarbus capito [13] and White shrimp Litopenaeus vannamei [14] are domesticated for saline-alkaline water culture. Due to the shrinking aquaculture space, thus expanding new aquaculture space for aquaculture development is essential, especially in saline-alkaline water.
The saline-alkaline water distributed in China are mainly three types, including chloride, carbonate, and sulfate, where the main ions are Na+, K+, Ca2+, Mg2+, Cl−, CO32-, HCO3-, OH− and SO42-, separately [15]. Meanwhile, different types of saline-alkaline water also have different ionic compositions. Cl− is the main anion of chloride alkalinity, while CO32- and HCO3- in carbonate alkalinity, SO42- in sulfate alkalinity are also observed [16]. Among these, Daqing area in Heilongjiang province is a typical saline-alkaline wetland with abundant carbonate alkalinity (NaHCO3) located in the western Songnen plain of China, where high carbonate alkalinity and pH in the saline-alkaline water are characteristics of the environment [17]. High carbonate alkalinity can reduce the concentration of H+ in the saline-alkaline water due to the high pH, thereby leading to the equilibrium state toward ammonia (NH3) direction NH4+ + OH− ⇌ NH3·H2O, and making the aquatic animals NH3 poisoning [18,19,20]. Consequently, the growth and quality of aquatic animals may be influenced significantly.
The Chinese mitten crab, Eriocheir sinensis, is an important aquatic animal with high economic and nutritional values. In addition, its aquaculture yield reached 815,318 t in 2022 [21]. E. sinensis is a migratory aquatic animal that grows in freshwater until it reaches sexual maturity and reproduction occurs in brackish water, thereby leading to high salinity tolerance [22]. Recent studies have also illustrated that E. sinensis has a high carbonate alkalinity tolerance characteristics [5,11]. However, the edible yield and quality of E. sinensis reared in carbonate alkalinity water outside are still unclear. Therefore, the aim of this study was to investigate the edible yield, coloration, nutritional and flavor quality of E. sinensis in carbonate alkalinity water.

2. Materials and Methods

2.1. Experimental set up and culture management

The E. sinensis was reared in carbonate alkalinity water from a local aquaculture demonstration farm (124.62°E, 45.70°N) in Zhaoyuan City of Heilongjiang Province, China. The culture experiment began on 1st May 2021 and completed on 30th September 2021. The megalopa Guanghe No. 1 was originated from Panjin Guanghe Crab Industry Co., Ltd., with the average body weight of juveniles 5.32±0.26 g/ind. These juveniles were reared in carbonate alkalinity water with stocking density 15000/ha, and the water quality parameters were as follows: intensive pond (IP), salinity 0.68±0.05 ppt, carbonate alkalinity 8.48±0.32 mmol/L, pH 8.72±0.04; semi intensive reed wetland (SIWR), salinity 0.56±0.02 ppt, carbonate alkalinity 8.88±0.04 mmol/L, and pH 8.65±0.04. IP was transplanted with Canadian pondweed, Elodea canadensis, while SIWR was planted with natural Phragmites australis. During the culture stage, the juveniles were fed twice a day at 8:00 a.m. and 5:00 p.m. with a commercial formulated diet (crude protein≥39.0%, crude fat≥5.0%, moisture≤12.0%, ash≤18.0%. Nantong Charoen Pokphand Co., Ltd., Nantong, China). The feeding amount accounted for approximately 2% of the total body weights.

2.2. Sample collection and dissection

All E. sinensis procedures in this study were conducted according to the Guidelines for the Care and Use of Laboratory Animals of Heilongjiang River Fisheries Research Institute (HRFRI), Chinese Academy of Fishery Sciences (CAFS), Harbin, China. The E. sinensis used in the present study were reviewed and approved by the Committee for the Welfare and Ethics of Laboratory Animals of HRFRI, CAFS. On 4th and 29th September 2021, a total of one hundred mature E. sinensis (♀:♂=1:1) reared in IP and SIWR were collected respectively. Subsequently, these alive E. sinensis were transported to HRFRI, CAFS, and then accurately weighed with an electronic balance (JA2002, Shanghai Puchun measuring instrument Co., Ltd., Shanghai, China), and the carapace length and carapace width were also measured with a Vernier caliper (605, Harbin measuring tools and cutting tools Co., Ltd., Harbin, China). The anatomical procedures were according to the previous study [5]. The hepatosomatic index (HSI, %), gonadosomatic index (GSI, %), meat yield (MY, %), total edible yield (TEY, %), and condition factor (CF, g/cm3) were calculated by the following equations (1-5):
GSI (%) = 100 × Gonad weight/Body weight
HSI (%) = 100 × Hepatopancreas weight/Body weight
MY (%) = 100 × Muscle weight/Body weight
TEY (%) = GSI (%) + HSI (%) + MY (%)
CF (g/cm3) = Body weight/Carapace length3

2.3. Measurements of color and nutritional parameters

The color parameters L* (brightness), a* (redness) and b* (yellowness) of carapace, hepatopancreas and female gonad (ovary) between IP and SIRW were measured by a colorimeter (CR-400, Konica Minolta, Marunouchi, Tokyo, Japan). The measured method was carried out by the Long et al ’s study [23]. The overall collected samples of each edible tissue were randomly selected and combined into three duplicate samples. The proximate composition, fatty acids, free amino acids, mineral elements of E. sinensis reared in IP and SIRW were measured by the previous study [24]. The hypocholesterolaemic/hypercholesterolaemic ratio (h/H), index of atherogenicity (AI), and index of thrombogenicity (TI) [25] were calculated using the following equations (6-8):
h/H=∑(18:1n9,18:1n7,18:2n6,18:3n6,18:3n3,20:3n6,20:4n
6,20:5n3,22:4n6,22:5n3,22:6n3)/∑(14:0,16:0)
AI=(12:0+4×14:0+16:0) / (∑n-6 PUFA+∑n-3
PUFA+∑MUFA)
TI=(14:0+16:0+18:0)/(0.5×∑MUFA+0.5×∑n-
6PUFA+3.0×∑n-3PUFA+n-3/n-6 PUFA)

2.4. Statistical analysis

The results are presented as the mean values ± standard error (SE). SPSS 22.0 software (SPSS Inc, Chicago, IL, USA) was used for statistical analysis. Independent samples t-test was used to determine the differences between IP and SIWR. The comparison test P< 0.05 was regarded as the statistical significance, and P< 0.01 was regarded as the extremely statistical significance.

3. Results

3.1. Total edible yield

The edible yield and condition factor of adult E. sinensis reared in carbonate alkalinity water are presented in Figure 1. For females, the HSI and CF in IP were significantly higher than those of SIRW, however, significantly lower GSI and TEY in IP were observed (P< 0.05, Figure 1A and C). There was significantly increasing tendency observed in male GSI, MY and TEY from IP to SIRW (P< 0.05, Figure 1B).

3.2. Color parameters

The color parameters of adult E. sinensis reared in carbonate alkalinity water are shown in Table 1. Significantly higher L* value of male dry carapace was observed in IP than that in SIRW (P< 0.05). For hepatopancreas, there were extremely significantly different b* values of female E. sinensis between IP and SIRW (P< 0.01), while significant differences were also observed by a* value of female wet hepatopancreas, L* value of male wet hepatopancreas, and b* values of male hepatopancreas (P< 0.05). No significant differences were found in ovary color between IP and SIRW (P> 0.05).

3.3. Proximate composition

The proximate composition of adult E. sinensis reared in carbonate alkalinity water are presented in Table 2. The contents of crude protein and crude fat in the female hepatopancreas in IP significantly increased compared with that in SIRW (P< 0.05). A significantly increasing tendency was observed by crude protein in male gonad from IP to SIRW (P< 0.05), while the content of crude protein in male muscle in IP was lower than that in SIRW, with an extremely significant difference (P< 0.01).

3.4. Fatty acids profiles

Table 3 illustrates the evaluation and comparison of the main fatty acid composition, concentration and disease index of adult E. sinensis reared in carbonate alkalinity water. For females, the higher concentrations of ∑SFA, ∑n-3 PUFA, ∑LC-PUFA, ∑DHA+EPA in all the edible tissues, ∑PUFA in the ovary and muscle were observed in SIRW than those in IP, with no significant difference (P> 0.05). The higher concentrations of ∑MUFA, ∑EFA, h/H in all the edible tissues were observed in IP than those in SIRW, with the following significant differences: ∑MUFA in the hepatopancreas and ovary, ∑EFA in the muscle, and h/H in the ovary (P< 0.05). For males, significantly increasing tendency was detected of ∑SFA in the gonad system and muscle, ∑PUFA in the gonad system, ∑n-3 PUFA in the muscle, ∑DHA+EPA in the hepatopancreas from IP to SIRW (P< 0.05). The higher concentrations of ∑MUFA, h/H in all the edible tissues, ∑EFA in the hepatopancreas and muscle were detected in IP than those in SIRW, with the following significant differences: ∑MUFA, ∑EFA of the hepatopancreas between IP and SIRW (P< 0.05), ∑MUFA of the gonad system and muscle, ∑EFA of muscle between IP and SIRW (P< 0.01).

3.5. Free amino acids composition and taste activity value

The composition and contents of free amino acids (FAAs) of adult E. sinensis reared in carbonate alkalinity water are presented in Table 4. With respect to females, the concentrations of Serine (Ser), Isoleucine (Ile), Lysine (Lys), Valine (Val) and ∑EFAA in the hepatopancreas significantly increased from SIRW to IP (P< 0.05), however, the higher concentrations of Alanine (Ala), Histidine (His), Lys, Methionine (Met) in the muscle were observed in SIRW compared with those in IP (P< 0.05). For males, significant differences were checked by Ile in the gonad system and ∑FAA in the muscle (P< 0.05), while extremely significant differences were also observed by Ala in the hepatopancreas and muscle, Glycine (Gly) in the muscle between IP and SIRW (P< 0.01).
The flavor characteristics and taste activity value (TAV) of adult E. sinensis reared in carbonate alkalinity water are shown in Table 5. The 17 FAAs were separated as two tastes including pleasant taste (umami and sweetness) and unpleasant taste (bitterness). The concentrations of ∑TUV and ∑TBV in the female hepatopancreas of IP were higher than those in SIRW, however, higher concentration of ∑TSV was observed in SIRW. Higher concentrations of ∑TSV and ∑TBV in the ovary were detected in SIRW than those in IP. In the muscle and male hepatopancreas , the ∑TUV, ∑TSV and ∑TBV values of IP were lower than those of SIRW.

3.6. Mineral element composition

The mineral element composition and contents of adult E. sinensis reared in carbonate alkalinity water are presented in Table 6. Regarding the hepatopancreas, there was no significant difference observed between IP and SIRW (P> 0.05). Significantly increasing tendency was detected in K, Ca, Mg, Fe, Zn of ovary from SIRW to IP (P< 0.05), meanwhile, the content of ∑TME in IP was extremely significantly different compared with that in SIRW (P< 0.01). The contents of K and Mg in female muscle, Na and ∑TME in male muscle were significantly increased from SIRW to IP (P< 0.05). Overall, the higher contents of hepatopancreas ∑TME were observed in SIRW, however, the contents of gonad and muscle ∑TME in IP were higher than those in SIRW.

4. Discussion

4.1. Total edible yield

The hepatopancreas, gonad and muscle are important edible tissues of E. sinensis. However, previous studies were focused on the total edible yield of E. sinensis reared in the freshwater [26,27], chloride or sulfate-type saline-alkaline water [28], while little literature was paid close attention to the E. sinensis reared in carbonate alkalinity water. The present study indicated that the E. sinensis can complete gonadal development normally compared with the previous studies [5,24]. The GSI value of female E. sinensis was 3.78±0.67% reared in IP on 4th September and 6.75±0.55% in SRW on 29th September, while the GSI value of female E. sinensis was 5.30±0.22% in freshwater pond on 15th September [24]. It has been demonstrated that usually the later the sampling period, the higher the GSI in the same location, which was consistent with the present study. The specific values between previous and present studies were different, which were mainly caused by the difference in water temperature and sampling period [5,24,26,27]. The MY and TEY values of female E. sinensis in present study were 26.11±0.67%, 26.53±0.28%, 38.19±0.98%, and 40.78±0.68%, respectively, indicating that E. sinensis reared in carbonate alkalinity water have similar MY and TEY values compared with that in the previous studies [5,26,27]. Overall, the above results showed that the E. sinensis reared in carbonate alkalinity water will not significantly affect the gonadal development and the total edible yield.

4.2. Color parameters

The color is one of the important indicators for sensory and quality evaluation of E. sinensis. In the cognition of consumers, the higher reddish values of the dried carapace and ovary, as well as the higher reddish and yellowish values of the wet hepatopancreas, suggest better quality [23]. It has been demonstrated that the reddish and yellowish parameters of E. sinensis tissues are significantly related to the deposition of carotenoids [29]. The present study illustrated that the b* values of the IP [female: 40.99±1.14; male: 45.85±1.10] and SIRW [female: 42.19±1.15; male: 43.29±0.88] freeze-dried E. sinensis carapace reared in carbonate alkalinity water were obviously higher than those of wild-caught mitten crabs in the natural Suifenhe and Nanliujinag delta [30], suggesting that E. sinensis reared in carbonate alkalinity water accumulated more carotenoids. Similar b* values of freeze-dried three-year-old E. sinensis carapace were also observed in the pond of Zhaodong city, Heilongjiang Province, China [24]. In addition, the higher b* values of the IP [52.01±0.19] and SIRW [51.34±0.87] freeze-dried E. sinensis ovary in the present study were also detected in carbonate alkalinity water compared with previous studies [24,30]. These results suggested that E. sinensis reared in carbonate alkalinity water accumulated more carotenoids and represented better quality.

4.3. Biochemical composition

The biochemical composition, especially crude protein, has become one of the most important indicators for evaluating the nutritional value of aquatic animals, and can be affected by numerous factors, such as the culture environment [24]. The present study demonstrated that although the culture environment of IP and SIRW were all belonged to the carbonate alkalinity water, significant differences were still observed between IP and SIRW. The crude protein of female IP [11.17±0.16%] and SIRW [9.63±0.10%] hepatopancreas were higher than those cultured in the Shandong, Qinghai, and Shanghai [26,28], wild mitten crabs caught in the Suifenhe, Liaohe, and Nanliujiang [30]. At the same time, the crude protein of E. sinensis gonad and muscle reared in carbonate alkalinity water were similar with those in the previous studies [24,26,28,30]. All these results illustrated that E. sinensis reared in carbonate alkalinity water was a good high-protein seafood source.

4.4. Fatty acids composition

The fatty acid composition and contents have also been one of the most important nutritional indicators for aquatic animals, particularly essential fatty acids (EFAs), and unsaturated fatty acids (UFAs) [24,30]. The present study showed that the total saturated fatty acids (∑SFA), total monounsaturated fatty acids (∑MUFA) and total polyunsaturated fatty acids (∑PUFA) of E. sinensis reared in carbonate alkalinity water were similar to those cultured in the other regions [24,27,28,30], implying that alkalinity water did not significantly alter the fatty acid composition of E. sinensis. It can be estimated that the fatty acid composition and content changes of the E. sinensis differential edible tissues should be mainly contributed by heredity, and then followed by culture environment and diet. The culture environment can slightly regulate the fatty acid contents other than that of composition.
Due to the fact that PUFAs are more beneficial to the human health, it has been received widespread attention, especially the DHA, EPA, and ARA [31]. Numerous studies have confirmed that DHA and EPA can play an important role in preventing inflammation and cardiovascular diseases, while ARA can promote the development of the central nervous system [31,32,33]. The present study demonstrated that alkalinity water affected the fatty acid contents of E. sinensis compared with previous studies [26,27]. Furthermore, increasing DHA, EPA, and ARA contents in males, but decreasing DHA and EPA contents in females were detected, implying the differential effects of alkalinity on genders of E. sinensis. These results were consistent with our previous studies [5]. As E. sinensis reared in the similar carbonate alkalinity water with differential culture type, the EPA and ARA contents of male hepatopancreas and muscle in SIRW were significantly increased compared with those in IP. This phenomenon can be explained by the different developmental stage, because the EPA and ARA contents of hepatopancreas and muscle increased with the GSI improvement [27]. The h/H, AI and TI are important indexes used to evaluate the beneficial effects of fatty acids on the human health [24,25]. Generally, the higher h/H, the lower AI and TI are illustrated to be better quality for human health. The three indexes of E. sinensis reared in carbonate alkalinity water were similar to the results of previous studies [24,30].

4.5. FAAs composition and TAV analysis

The FAAs composition and contents are one of the important factors affecting the taste and quality of crustaceans [24]. The present study illustrated that the ∑EFAA [IP: (724.11±14.76) mg/100 g; SIRW: (632.4±5.94) mg/100 g] and ∑FAA [IP: (1937.29±85.06) mg/100 g; SIRW: (1788.67±146.25) mg/100 g] contents of female E. sinensis hepatopancreas reared in carbonate alkalinity water were higher than wild-caught mitten crabs [30], and three-year-old E. sinensis [24], indicating better taste quality. These results were consistent with our previous studies, in which the prolonged alkalinity stress can improve the ∑EFAA and ∑FAA contents [5]. In terms of specific amino acid, differential amino acids present different taste characteristics, while the taste characteristics, TAV, is positively corelated with the ratio between the special amino acid value and its threshold. Table 5 showed that the main umami amino acid Glu, sweetness amino acid Ala were similar to previous studies [24,28,30]. Although we have classified Arg as a bitter amino acid, the flavor characteristics of Arg is actually significantly related to its concentration, with low concentration exhibiting bitterness and high concentration exhibiting umami [34]. The present study illustrated that the Arg content [IP: 7.42; SIRW: 6.50] in the female hepatopancreas was slightly higher than that of previous studies [5,24,30]. In addition, the ∑TUV, ∑TSV and ∑TBV values of female hepatopancreas were higher than those in the pond-reared and wild-caught mitten crabs [24,30], suggesting stronger flavor characteristics.

4.6. Mineral element analysis

Mineral elements are important nutritional substances required to maintain normal growth, development, and metabolism of the human beings, ensuring normal life activities [35]. Na, K, Ca, and Mg are macro-elements required by the human body and play differential roles for human health. Among these four macro-elements, Na and K play an important role in maintaining the acid-base balance and osmotic pressure of blood and body fluids. Ca is an important component of human bones and teeth. Mg participates in energy metabolism in the human body, catalyzes and activates various enzyme systems, and plays an important role in preventing cardiovascular diseases [36]. Of all the E. sinensis edible tissues, Na and K contents were significantly higher than other macro-elements, which was consistent with previous studies [24,37]. In addition, the K content was higher than that of Na content except for the testis, implying that the culture environment perhaps have influence on the Na and K accumulation. Fe, Zn, Cu and Mn are micro-elements required by the human body. Among these, Fe plays an important role in the body's hematopoietic, oxygen transport, and fluid balance. Zn is an important coenzyme factor in the human body and is involved in the synthesis of DNA, RNA and proteins. Cu can promote the production of hemoglobin in humans. Mn plays an important role in the central nervous system of the human brain [37]. The higher Fe content in the E. sinensis hepatopancreas was observed compared with that in the gonad and muscle tissues, which is an important Fe source for the human and has a certain significance in preventing iron deficiency anemia. The higher Zn contents in the E. sinensis ovary and muscle were checked compared with that in the testis and hepatopancreas tissues. Above results illustrated that E. sinensis reared in carbonate alkalinity water was a good source of mineral elements.

5. Conclusions

The present study investigated the gonadal development, edible yield, coloration, nutritional and flavor quality of E. sinensis reared in carbonate alkalinity water (IP and SIRW culture model ). Due to the sampling time, the differential GSI and TEY values of E. sinensis were observed between IP and SIRW. IP accumulated more ∑MUFA, ∑EFA, h/H in the female edible tissues compared with those of SIRW, whereas SIRW had better ∑FAA content of muscle. IP also achieved more mineral elements, such as K, Ca, Mg, Fe, Zn in the ovary. In summary, the E. sinensis reared in carbonate alkalinity water can complete the gonadal development, accumulate more carotenoids, rich in fatty acids, FFAs, and mineral elements, which are important nutritional sources.

Author Contributions

Conceptualization, S.W. and Z.Z.; Methodology, S.W. and Z.Z.; Software, S.W. and L.L.; Validation, R.Z. and Y.S.; Formal Analysis, S.W., R.Z. and K.G.; Investigation, S.W. and L.L.; Resources, Z.Z.; Data Curation, S.W. and K.G.; Writing–Original Draft Preparation, S.W.; Writing–Review & Editing, S.W. and Z.Z.; Visualization, R.Z. and Y.S.; Supervision, Z.Z.; Project Administration, Z.Z.; Funding Acquisition, Z.Z.

Funding

This work was supported by the National Key Research and Development Project (2023YFD2401003), Central Public-interest Scientific Institution Basal Research Fund (2023TD59). The APC was funded by NO. 2023YFD2401003.

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

The data presented in this study are available on request from the corresponding author.

Conflicts of Interest

The authors declare no conflict of interest.

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Preprints 95473 g001
Figure 1. The edible yield (% body weight, A and B) and condition factor (%, C) of adult Eriocheir sinensis reared in carbonate alkalinity water. Data are presented as means ± standard error (SE) (n=25). *denotes significant difference (P< 0.05), **denotes extremely significant difference (P< 0.01). IP, Eriocheir sinensis reared in intensive pond; SIRW, Eriocheir sinensis reared in semi intensive reed wetland; HSI, hepatosomatic index; GSI, gonadosomatic index; MY, muscle yield; TEY, total edible yield.
Figure 1. The edible yield (% body weight, A and B) and condition factor (%, C) of adult Eriocheir sinensis reared in carbonate alkalinity water. Data are presented as means ± standard error (SE) (n=25). *denotes significant difference (P< 0.05), **denotes extremely significant difference (P< 0.01). IP, Eriocheir sinensis reared in intensive pond; SIRW, Eriocheir sinensis reared in semi intensive reed wetland; HSI, hepatosomatic index; GSI, gonadosomatic index; MY, muscle yield; TEY, total edible yield.
Preprints 95473 g001
Table 1. The color comparison of adult Eriocheir sinensis reared in carbonate alkalinity water.
Table 1. The color comparison of adult Eriocheir sinensis reared in carbonate alkalinity water.
Item Color Female Male
IP SIRW IP SIRW
Carapace Wet sample L* 47.18±0.99 48.57±0.95 47.78±0.70 49.51±1.13
a* 2.76±0.29 2.78±0.21 3.26±0.24 3.26±0.40
b* 15.04±0.39 16.59±0.77 16.08±0.48 17.70±0.62
Dry sample L* 67.09±1.15 64.89±0.95 70.16±1.00* 65.80±1.11
a* 21.30±0.96 21.29±1.02 20.79±1.12 20.95±1.53
b* 40.99±1.14 42.19±1.15 45.85±1.10 43.29±0.88
Hepatopancreas Wet sample L* 62.22±1.61 61.52±1.25 54.65±2.18 62.46±2.18*
a* 15.52±1.89 21.65±1.31* 16.90±1.13 16.59±1.33
b* 43.38±2.94 54.23±1.32** 39.46±2.42 48.41±2.48*
Dry sample L* 60.60±2.73 63.99±2.12 57.31±4.01 64.41±1.43
a* 12.53±3.25 15.43±1.42 14.01±1.48 13.22±0.92
b* 37.49±1.49 48.43±1.26** 35.17±1.31 45.26±2.37*
Gonad Wet sample L* 28.55±0.48 28.25±0.32 —— ——
a* 1.78±0.67 1.22±0.27 —— ——
b* 3.96±0.41 3.88±0.24 —— ——
Dry sample L* 74.96±1.77 73.96±0.54 —— ——
a* 30.93±2.00 32.31±0.86 —— ——
b* 52.01±0.19 51.34±0.87 —— ——
Note: Data are presented as means ± standard error (SE) (n=25). “——”means no detection. *denotes significant difference (P< 0.05), **denotes extremely significant difference (P< 0.01). Abbreviations: IP, Eriocheir sinensis reared in intensive pond; SIRW, Eriocheir sinensis reared in semi intensive reed wetland.
Table 2. The proximate composition of adult Eriocheir sinensis reared in carbonate alkalinity water (%, wet weight).
Table 2. The proximate composition of adult Eriocheir sinensis reared in carbonate alkalinity water (%, wet weight).
Item Female Male
IP SIRW IP SIRW
Hepatopancreas
Moisture 48.74±5.16 61.72±3.17 61.18±1.82 62.32±1.69
Crude protein 11.17±0.16* 9.63±0.10 8.79±1.46 8.51±1.03
Crude fat 35.39±0.05* 23.79±1.21 25.21±1.88 25.11±1.45
Ash 1.31±0.08 1.57±0.27 1.09±0.19 1.17±0.19
Gonad
Moisture 56.46±2.89 55.25±2.66 76.08±0.62 75.05±0.77
Crude protein 28.90±0.23 28.83±0.10 15.90±0.06 16.62±0.09*
Crude fat 6.42±0.50 7.23±0.02 0.72±0.07* 0.37±0.02
Ash 1.89±0.11 1.83±0.04 2.08±0.05 2.20±0.05
Muscle
Moisture 78.63±0.67 79.73±0.55 83.69±0.56 82.29±0.35
Crude protein 17.76±0.16 17.46±0.03 13.64±0.06 15.07±0.06**
Crude fat 0.50±0.03 0.42±0.03 0.44±0 0.39±0.02
Ash 1.44±0.03 1.54±0.02 1.38±0.01 1.48±0.08
Notes: Data are presented as means ± standard error (SE) (n=3). * denotes significant difference (P<0.05), ** denotes extremely significant difference (P< 0.01). Abbreviations: IP, Eriocheir sinensis reared in intensive pond; SIRW, Eriocheir sinensis reared in semi intensive reed wetland.
Table 3. The fatty acid composition in hepatopancreas, gonad and muscle of adult Eriocheir sinensis reared in carbonate alkalinity water (% of total fatty acids).
Table 3. The fatty acid composition in hepatopancreas, gonad and muscle of adult Eriocheir sinensis reared in carbonate alkalinity water (% of total fatty acids).
Fatty acid Hepatopancreas Gonad Muscle
IP SIRW IP SIRW IP SIRW
Female
C14:0 1.51±0.17 2.17±0.47 0.79±0.03 1.20±0.08* 0.33±0.05 0.51±0.05
C15:0 0.63±0.03 1.31±0.34 0.47±0.06 0.93±0.10 0.27±0.02 0.47±0.04*
C16:0 22.26±0.73 23.01±1.24 16.59±0.39 17.73±0.59 12.96±0.40 13.73±0.51
C17:0 0.61±0.01 1.34±0.14* 0.50±0.06 0.77±0.04 0.73±0.07 1.34±0.14
C18:0 3.14±0.13 3.72±0.34 2.72±0.09 3.05±0.14 8.98±0.01 9.33±0.20
C20:0 0.32±0.02 0.41±0.03 0.09±0.01 0.13±0 0.17±0.02 0.28±0.01*
∑SFA 29.24±1.11 33.24±2.72 21.25±0.63 24.06±0.47 23.42±0.57 25.65±0.54
C15:1n5 0.23±0.02 0.45±0.10 0.15±0 0.26±0.02* 0.85±0.09 0.78±0.06
C16:1n7 8.38±0.30 10.95±0.34* 11.40±0.01 13.65±1.04 3.04±0.21 4.26±0.18*
C18:1n9 39.15±0.15** 32.45±0.40 33.69±1.13* 26.10±1.12 25.92±0.65 22.20±0.63
C20:1n9 1.07±0.03 1.28±0.10 0.45±0.02 0.34±0.03 0.71±0.07 0.81±0.09
∑MUFA 49.42±0.43* 45.89±0.27 46.07±1.09* 40.51±0.07 30.51±1.01 28.04±0.48
C18:2n6 15.81±0.20* 11.56±0.78 17.19±0.80 13.87±0.84 13.46±0.87* 8.71±0.09
C18:3n3 2.17±0.04 2.93±0.51 3.78±0.58 6.21±1.39 1.89±0.05 2.73±0.14*
C20:2n6 0.95±0.26 0.88±0.02 0.95±0.06 0.81±0.05 1.50±0.11 1.47±0.06
C20:4n6 (ARA) 0.65±0.10 1.55±0.43 2.33±0.19 3.85±0.18* 5.40±0.42 8.14±0.47*
C20:3n3 0.24±0.06 0.48±0.08 0.38±0.03 0.55±0.08 0.43±0.03 0.74±0.05*
C20:5n3 (EPA) 0.77±0.12 1.61±0.60 4.72±0.53 6.68±0.12 14.05±0.19 16.21±1.16
C22:6n3 (DHA) 0.48±0.04 1.28±0.62 3.20±0.10 2.82±0.01 9.18±0.86 7.92±0
∑PUFA 21.29±0.72 20.89±2.98 32.85±0.51 35.34±0.53 46.08±1.57 46.67±0.65
∑EFA 17.97±0.24 14.48±1.28 20.97±0.22 20.07±0.55 15.35±0.81* 11.44±0.05
∑LC-PUFA 3.32±0.48 6.21±1.71 11.71±0.81 14.99±0.04 30.55±0.77 34.74±0.63
∑n-3 PUFA 3.65±0.18 6.29±1.27 12.08±0.87 16.26±1.11 25.54±0.72 27.59±0.95
∑n-6 PUFA 17.65±0.27 14.60±0.68 20.78±0.42 19.09±0.60 20.55±0.31 19.08±0.40
n-3/n-6 PUFA 0.21±0.01 0.42±0.09 0.58±0.08 0.86±0.13 1.24±0.02 1.45±0.12
∑DHA+EPA 1.25±0.15 2.89±1.22 7.92±0.62 9.50±0.11 23.22±1.05 24.13±1.16
DHA/EPA 0.63±0.04 0.76±0.11 0.68±0.06* 0.42±0.01 0.65±0.05 0.49±0.04
h/H 2.48±0.12 2.06±0.27 3.72±0.12* 3.15±0.05 5.23±0.23 4.65±0.18
AI 0.40±0.03 0.48±0.07 0.25±0.01 0.30±0.01 0.19±0.01 0.21±0.01
TI 0.60±0.04 0.60±0.11 0.29±0 0.28±0.02 0.22±0.01 0.22±0.01
Male
C14:0 1.35±0.16 1.59±0.22 0.37±0.03 0.48±0.04 0.26±0.01 0.36±0.01**
C15:0 0.70±0.05 0.89±0.13 0.28±0.07 0.30±0.02 0.25±0.01 0.43±0.03*
C16:0 22.16±0.12 21.49±1.23 9.26±0.27 10.43±0.33 12.93±0.11 13.18±0.49
C17:0 0.53±0.05 0.94±0.02* 0.62±0.02 0.92±0.10 0.76±0.03 1.33±0**
C18:0 3.37±0.01 3.26±0.10 8.06±0.05 7.92±0.26 9.04±0.18 9.90±0.06*
C20:0 0.37±0 0.34±0.02 0.25±0 0.26±0.01 0.17±0.01 0.26±0**
∑SFA 29.52±0.33 29.53±0.88 19.32±0.32 20.70±0.02* 23.39±0.11 25.45±0.46*
C15:1n5 0.25±0.02 0.24±0.13 0.93±0.05 0.73±0.08 1.08±0.03 1.02±0.02
C16:1n7 7.79±0.99 10.79±1.18 2.03±0.27 2.31±0.10 2.03±0.11 2.64±0.04*
C18:1n9 36.24±0.77* 31.27±0.62 23.88±0.24 23.19±0.17 25.31±0.07** 20.52±0.16
C20:1n9 1.09±0.05 1.01±0.04 1.34±0.04 1.22±0.10 0.79±0.01 0.79±0.07
∑MUFA 46.03±0.21* 43.86±0.43 35.91±0.02** 30.20±0.43 29.20±0.06** 24.96±0.25
C18:2n6 19.19±0.04* 14.51±0.79 9.84±0.79 10.13±3.01 12.10±0.21* 8.59±0.35
C18:3n3 1.98±0.07 3.35±0.89 1.00±0.09 1.60±0.17 1.40±0.04 2.10±0.27
C20:2n6 0.76±0.19 0.86±0.04 3.17±0.11* 2.34±0.08 1.80±0.01 1.61±0.11
C20:4n6 (ARA) 0.65±0.11 2.11±0.28* 11.78±0.63 15.16±0.52 6.92±0.15 9.96±0.70*
C20:3n3 0.17±0.03 0.52±0.16 0.61±0.02 0.80±0.09 0.44±0.01 0.70±0.03**
C20:5n3 (EPA) 0.83±0.08 2.20±0.23* 11.13±0.10 12.35±1.31 14.74±0.09 16.18±0.02**
C22:6n3 (DHA) 0.67±0.23 2.38±0.41 6.81±0.37 5.98±0.72 9.82±0.09 9.85±0.58
∑PUFA 24.45±0.54 26.62±1.31 44.78±0.31 49.10±0.45* 47.41±0.06 49.59±0.72
∑EFA 21.17±0.11** 17.86±0.11 10.84±0.88 11.73±3.18 13.50±0.17* 10.67±0.62
∑LC-PUFA 3.29±0.64 8.59±1.21 33.70±1.19 36.93±2.73 33.71±0.13 38.56±1.41
∑n-3 PUFA 3.65±0.19 8.44±1.20 19.55±0.28 20.72±1.37 26.39±0.03 28.82±0.30*
∑n-6 PUFA 20.80±0.16* 18.18±0.22 25.23±0.05 28.38±1.38 21.02±0.05 20.78±0.43
n-3/n-6 PUFA 0.18±0.01 0.47±0.10 0.78±0.02 0.74±0.13 1.26±0.01 1.39±0.01*
∑DHA+EPA 1.50±0.31 4.58±0.65* 17.94±0.47 18.32±2.02 24.56±0 26.03±0.59
DHA/EPA 0.79±0.20 1.08±0.07 0.61±0.03 0.48±0.01 0.67±0.01 0.61±0.03
h/H 2.52±0.08 2.44±0.18 6.65±0.21 6.26±0.13 5.30±0.04 4.97±0.21
AI 0.39±0.01 0.40±0.01 0.13±0.01 0.16±0 0.18±0 0.20±0.01
TI 0.60±0.02 0.47±0.06 0.20±0.01 0.20±0.01 0.21±0 0.21±0.01
Notes: Data are presented as means ± standard error (SE) (n=3). * denotes significant difference (P< 0.05). ** denotes extremely significant difference (P< 0.01). Abbreviations: IP, Eriocheir sinensis reared in intensive pond; SIRW, Eriocheir sinensis reared in semi intensive reed wetland;∑SFA, total saturated fatty acids; ∑MUFA, total monounsaturated fatty acids; ∑PUFA, total polyunsaturated fatty acids; ∑EFA, total essential fatty acids; ∑LC-PUFA, total long chain polyunsaturated fatty acids; ∑n-3 PUFA, total ω-3 polyunsaturated fatty acids; ∑n-6 PUFA, total ω-6 polyunsaturated fatty acids; DHA, docosahesaenoic acid; EPA, eicosapentaenoic acid, ARA, arachidonic acid; h/H, hypocholesterolaemic/hypercholesterolaemic ratio; AI, index of atherogenicity; TI, index of thrombogenicity.
Table 4. The free amino acid composition in hepatopancreas, gonad and muscle of adult Eriocheir sinensis reared in carbonate alkalinity water (mg/100 g, wet weight).
Table 4. The free amino acid composition in hepatopancreas, gonad and muscle of adult Eriocheir sinensis reared in carbonate alkalinity water (mg/100 g, wet weight).
Free amino acids Hepatopancreas Gonad Muscle
IP SIRW IP SIRW IP SIRW
Female
Aspartic acid 61.64±1.28 41.42±6.26 2.80±0.54 3.45±0.50 2.18±0.27 2.94±0.31
Arginine 370.76±18.22 324.80±57.25 222.08±11.32 274.41±6.80 556.48±11.41 548.28±35.14
Alanine 233.89±25.35 285.79±53.52 100.10±10.94 137.58±3.70 338.37±8.75 530.03±25.96*
Cysteine 17.16±0.92 14.76±2.11 2.68±0.76 2.73±0.27 2.17±0.18 1.68±0
Glutamic acid 135.80±11.69 113.99±0.14 97.72±7.99 86.44±5.72 33.63±3.46 46.17±14.28
Glycine 130.66±21.38 133.69±24.05 60.24±5.88 64.19±10.08 347.70±24.21 453.18±78.36
Histidine 43.34±7.62 39.31±4.41 27.93±4.53 32.22±5.14 22.88±2.42 35.61±1.30*
Proline 92.75±16.01 107.32±23.94 71.14±5.25 73.86±2.83 135.70±7.48 147.75±23.28
Serine 28.33±0.66* 21.30±0.68 8.21±0.55 9.60±1.23 9.94±1.17 12.84±1.79
Tyrosine 98.84±8.62 73.88±3.42 18.61±1.70 19.23±1.67 18.08±2.52 20.06±2.60
Isoleucine▲ 67.41±0.04* 60.24±1.08 9.32±1.38 10.26±2.22 8.61±0.03 13.76±3.10
Leucine▲ 156.88±3.55 130.35±6.04 13.60±1.94 14.58±2.94 15.91±0.94 27.06±6.37
Lysine▲ 155.55±1.00* 138.35±3.31 38.97±9.97 43.95±11.31 28.99±0.07 39.34±0.96**
Methionine▲ 50.09±0.52 51.19±1.91 22.30±2.65 22.31±5.50 24.28±2.51 43.56±3.02*
Phenylalanine▲ 92.75±4.09 74.59±2.04 15.49±2.05 15.18±2.40 11.57±1.02 14.83±1.23
Threonine▲ 94.83±5.28 85.27±7.19 66.20±6.70 94.49±5.91 25.18±0 32.52±10.71
Valine▲ 106.61±2.37* 92.42±1.26 26.09±3.65 28.94±4.53 21.70±0.40 31.46±5.97
∑EFAA 724.11±14.76* 632.4±5.94 191.98±28.34 229.71±34.81 136.24±2.23 202.54±31.35
∑FAA 1937.29±85.06 1788.67±146.25 803.48±77.8 933.42±45.92 1603.38±9.64 2001.07±162.46
PETFAA 37.42±0.89 35.62±3.24 23.77±1.22 24.49±2.52 8.50±0.19 10.06±0.75
Male
Aspartic acid 43.85±3.26 48.34±24.86 24.44±3.22 28.43±5.07 2.27±0.56 2.74±0.04
Arginine 188.15±29.12 266.95±79.80 60.46±5.69 47.63±7.49 408.25±8.95 451.24±24.15
Alanine 139.45±13.65 318.65±0.04** 97.27±5.28 100.84±10.70 331.50±8.40 471.54±7.67**
Cysteine 8.73±1.51 16.25±8.61 1.44±0.14 2.31±0.58 3.06±0.07* 1.83±0.12
Glutamic acid 94.93±3.21 114.46±46.49 68.52±0.56 49.61±5.25 53.15±0.61 53.69±1.81
Glycine 79.84±1.00 135.22±48.32 43.29±6.29 42.69±3.20 321.59±12.02 465.93±6.64**
Histidine 30.11±0.21 41.39±11.40 8.26±1.31 6.97±0.41 22.76±1.25 25.80±1.42
Proline 66.41±2.52 93.25±8.48 61.24±4.80 41.13±1.57 97.51±6.49 121.40±22.25
Serine 17.96±1.13 22.84±7.64 3.11±0.07* 2.30±0.14 6.54±0.84 7.81±1.76
Tyrosine 70.26±1.48 83.70±39.02 17.70±0.46 18.37±1.92 26.17±4.63 23.25±1.65
Isoleucine▲ 37.64±2.23 64.30±29.24 7.64±0.37 11.55±0.52* 14.99±2.55 12.50±0.52
Leucine▲ 99.65±11.15 138.90±64.09 11.01±0.50 13.65±1.10 24.63±3.85 23.31±0.68
Lysine▲ 91.37±13.89 145.85±67.58 13.49±2.08 12.36±1.65 41.75±4.79 30.91±2.93
Methionine▲ 36.67±2.62 53.00±23.41 7.50±1.90 11.32±0.43 31.16±3.14 32.16±3.17
Phenylalanine▲ 60.00±2.35 81.29±37.07 10.27±0.29 13.43±1.35 14.21±1.94 16.85±1.25
Threonine▲ 57.42±2.41 85.36±25.80 15.66±2.54 10.54±0.89 35.47±2.69 27.29±2.66
Valine▲ 60.49±5.91 94.62±36.67 17.26±0.96 17.16±1.50 34.95±1.08 30.06±0.48
∑EFAA 443.23±40.57 663.33±283.85 82.82±8.64 90.01±7.45 197.17±8.38 173.08±5.84
∑FAA 1182.92±95.24 1804.37±558.45 468.56±25.61 430.3±43.77 1469.95±5.52 1798.31±56.21*
PETFAA 37.44±0.42 35.27±4.81 17.63±0.88 20.96±0.40 13.42±0.62* 9.62±0.02
Notes: Data are presented as means ± standard error (SE) (n=3). ▲ essential amino acid. * denotes significant difference (P< 0.05). ** denotes extremely significant difference (P< 0.01). Abbreviations: IP, Eriocheir sinensis reared in intensive pond; SIRW, Eriocheir sinensis reared in semi intensive reed wetland; ∑EFAA, total essential free amino acids; ∑FAA, total free amino acids; PETFAA, percentage of ∑EFAA to ∑FAA.
Table 5. The threshold and taste activity value of free amino acid composition in hepatopancreas, gonad and muscle of adult Eriocheir sinensis reared in carbonate alkalinity water.
Table 5. The threshold and taste activity value of free amino acid composition in hepatopancreas, gonad and muscle of adult Eriocheir sinensis reared in carbonate alkalinity water.
Free amino acids Flavor characteristics Threshold (mg/100 mL) Hepatopancreas Gonad Muscle
IP SIRW IP SIRW IP SIRW
Female
Aspartic acid umami (+) 100 0.62 0.41 0.03 0.03 0.02 0.03
Glutamic acid umami (+) 30 4.53 3.80 3.26 2.88 1.12 1.54
∑TUV 5.14 4.21 3.29 2.92 1.14 1.57
Alanine sweetness (+) 60 3.90 4.76 1.67 2.29 5.64 8.83
Glycine sweetness (+) 130 1.01 1.03 0.46 0.49 2.67 3.49
Serine sweetness (+) 150 0.19 0.14 0.05 0.06 0.07 0.09
Threonine sweetness (+) 260 0.36 0.33 0.25 0.36 0.10 0.13
Proline sweetness/bitterness (+) 300 0.31 0.36 0.24 0.25 0.45 0.49
∑TSV 5.77 6.62 2.68 3.46 8.93 13.02
Arginine sweetness/bitterness (-) 50 7.42 6.50 4.44 5.49 11.13 10.97
Lysine sweetness/bitterness (-) 50 3.11 2.77 0.78 0.88 0.58 0.79
Valine sweetness/bitterness (-) 40 2.67 2.31 0.65 0.72 0.54 0.79
Methionine bitterness/sweetness/sulphur (-) 30 1.67 1.71 0.74 0.74 0.81 1.45
Histidine bitterness (-) 20 2.17 1.97 1.40 1.61 1.14 1.78
Isoleucine bitterness (-) 90 0.75 0.67 0.10 0.11 0.10 0.15
Leucine bitterness (-) 190 0.83 0.69 0.07 0.08 0.08 0.14
Phenylalanine bitterness (-) 90 1.03 0.83 0.17 0.17 0.13 0.16
∑TBV 19.60 17.40 8.40 9.80 14.50 16.20
Male
Aspartic acid umami (+) 100 0.44 0.48 0.24 0.28 0.02 0.03
Glutamic acid umami (+) 30 3.16 3.82 2.28 1.65 1.77 1.79
∑TUV 3.60 4.30 2.53 1.94 1.79 1.82
Alanine sweetness (+) 60 2.32 5.31 1.62 1.68 5.52 7.86
Glycine sweetness (+) 130 0.61 1.04 0.33 0.33 2.47 3.58
Serine sweetness (+) 150 0.12 0.15 0.02 0.02 0.04 0.05
Threonine sweetness (+) 260 0.22 0.33 0.06 0.04 0.14 0.10
Proline sweetness/bitterness (+) 300 0.22 0.31 0.20 0.14 0.33 0.40
∑TSV 3.50 7.14 2.24 2.20 8.50 12.00
Arginine sweetness/bitterness (-) 50 3.76 5.34 1.21 0.95 8.17 9.02
Lysine sweetness/bitterness (-) 50 1.83 2.92 0.27 0.25 0.84 0.62
Valine sweetness/bitterness (-) 40 1.51 2.37 0.43 0.43 0.87 0.75
Methionine bitterness/sweetness/sulphur (-) 30 1.22 1.77 0.25 0.38 1.04 1.07
Histidine bitterness (-) 20 1.51 2.07 0.41 0.35 1.14 1.29
Isoleucine bitterness (-) 90 0.42 0.71 0.08 0.13 0.17 0.14
Leucine bitterness (-) 190 0.52 0.73 0.06 0.07 0.13 0.12
Phenylalanine bitterness (-) 90 0.67 0.90 0.11 0.15 0.16 0.19
∑TBV 11.40 16.80 2.80 2.70 12.50 13.20
Note: + means pleasant taste; − means unpleasant taste. Abbreviations: IP, Eriocheir sinensis reared in intensive pond; SIRW, Eriocheir sinensis reared in semi intensive reed wetland; ∑TUV, total umami values; ∑TSV, total sweetness values; ∑TBV, total bitterness values.
Table 6. The mineral element composition in hepatopancreas, gonad and muscle of adult Eriocheir sinensis reared in carbonate alkalinity water (mg/kg, wet weight).
Table 6. The mineral element composition in hepatopancreas, gonad and muscle of adult Eriocheir sinensis reared in carbonate alkalinity water (mg/kg, wet weight).
Element Hepatopancreas Gonad Muscle
IP SIRW IP SIRW IP SIRW
Female
Na 1635.77±148.67 1710.28±312.14 2113.71±440.18 1061.98±78.54 3027.63±495.63 2472.82±56.59
K 2407.05±82.20 2642.24±599.61 2715.20±201.54* 2090.29±72.20 3947.00±129.33* 3383.32±118.73
Ca 488.47±97.24 835.46±147.10 487.54±65.58* 230.54±26.95 1135.93±93.36 894.56±73.72
Mg 349.11±22.89 367.95±77.81 1514.93±100.57* 705.99±102.58 696.91±50.97* 491.37±11.33
Fe 79.48±8.06 79.82±9.65 41.61±4.00* 15.42±4.82 10.28±0.46 9.78±0.24
Zn 14.43±0.88 13.74±0.79 59.64±6.92* 32.65±1.53 42.05±1.27 39.76±1.36
Cu 5.98±1.41 6.29±1.16 5.97±1.36 5.05±0.40 9.87±0.53 6.63±1.19
Mn 3.69±0.67 1.61±0.34 4.66±1.51 2.48±0.44 0.63±0.02 0.66±0.01
∑TME 4983.97±319.40 5657.39±1101.56 6943.27±592.93** 4144.40±33.23 8870.30±763.43 7298.90±167.45
Male
Na 1626.64±411.30 1567.84±306.79 4430.63±240.01 4502.20±49.07 3459.41±235.32* 1977.00±317.44
K 2414.57±490.21 2510.66±367.45 3397.72±166.22 2954.14±616.72 3617.96±328.32 2828.30±229.34
Ca 467.16±170.51 780.07±114.32 1129.46±76.44 1064.87±160.05 1084.10±88.74 869.42±150.51
Mg 324.33±79.49 256.74±34.56 554.40±45.71 513.87±5.79 607.20±76.02 456.52±34.59
Fe 108.43±11.12 115.75±17.56 8.47±1.03 8.05±1.40 10.10±1.35 14.08±3.65
Zn 12.20±4.04 14.97±2.14 12.11±1.68 10.38±1.39 31.96±8.21 35.04±0.73
Cu 4.54±1.94 4.04±1.28 5.06±1.03 5.71±0.91 5.90±1.83 5.04±0.69
Mn 3.68±0.61 3.14±0.80 3.55±0.42 3.52±0.44 0.80±0.23 1.21±0.63
∑TME 4961.54±1142.91 5253.21±814.49 9541.40±194.67 9062.75±514.79 8817.43±664.45* 6186.61±612.24
Notes: Data are presented as means ± standard error (SE) (n=3). * denotes significant difference (P< 0.05). ** denotes extremely significant difference (P< 0.01). Abbreviations: IP, Eriocheir sinensis reared in intensive pond; SIRW, Eriocheir sinensis reared in semi intensive reed wetland; ∑TME, total mineral elements.
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