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Communication

Sex Hormones in Hemolymph of Red King Crabs from the Barents Sea

by
Alexander G. Dvoretsky
1,*,
Elena V. Tipisova
2,
Aleksandra E. Elfimova
2,
Viktoria A. Alikina
2 and
Vladimir G. Dvoretsky
1
1
Murmansk Marine Biological Institute (MMBI), 183010 Murmansk, Russia
2
N. Laverov Federal Center for Integrated Arctic Research of the Ural Branch of the Russian Academy of Sciences (FECIAR UrB RAS), 163000 Arkhangelsk, Russia
*
Author to whom correspondence should be addressed.
Animals 2021, 11(7), 2149; https://doi.org/10.3390/ani11072149
Submission received: 25 June 2021 / Revised: 17 July 2021 / Accepted: 18 July 2021 / Published: 20 July 2021
(This article belongs to the Special Issue Aquatic Animals: New Horizons for Blue Growth)
Browse Figures
Figure 1
<p>Study area in the southern Barents Sea.</p> "> Figure 2
<p>Carapace length and weight variations in the Barents Sea red king crabs analyzed for sex hormones.</p> "> Figure 3
<p>Variations of sex hormones in immature and mature red king crabs from the coastal zone of the Barents Sea. Green and red circles are outliers.</p> "> Figure 4
<p>Seasonal variations in vertebrate-type sex hormones in hemolymph of red king crabs from the Barents Sea. Green circles are outliers. Bars with the same letter are not significantly different (<span class="html-italic">p</span> &gt; 0.05).</p> ">
Versions Notes

Abstract

:

Simple Summary

Well-known sex hormones, testosterone and 17β-estradiol, play a crucial role in the reproduction of vertebrates. Biochemical assays have detected these substances in a few crustaceans, and it has been hypothesized that these hormones are involved in the regulation of crustacean reproduction. Red king crab is a large commercially important species harvested both in their native areas (North Pacific) and in the area of its introduction (Barents Sea). The presence of 17β-estradiol and testosterone and fluctuations of their concentrations in relation to different factors have not yet been investigated. For this reason, we provided a pilot study to reveal the levels of sex hormones in hemolymph of red king crabs captured in the coastal Barents Sea. These hormones were detected in the crabs and we compared our data with previously published data involving a wide range of crustaceans. We found seasonal variations in the level of testosterone with the maximum in the spawning period. Our data expand the current knowledge about the red king crab physiology and may be used for the development of its aquaculture.

Abstract

The presence of vertebrate-related steroid sex hormones has been reported in both freshwater and marine crustaceans. However, despite the commercial importance of king crabs, many aspects of their endocrinology are still unknown. For this reason, we examined hemolymph samples of the red king crab Paralithodes camtschaticus from the Barents Sea population for the presence of testosterone and 17β-estradiol using radioimmunoassay. The mean testosterone concentration was 0.46 ± 0.04 (range 0.08–1.39) ng mL–1, whereas the mean 17β-estradiol concentration was 1248.9 ± 91.4 (range 217.7–4100.1) pg mL–1. In general, the levels of 17β-estradiol and testosterone in red king crabs were higher than reported for the hemolymph of amphipods, crabs, and shrimps from warm and temperate waters, probably because the king crabs analyzed were larger and heavier than the other crustaceans. The concentrations of sex steroids did not differ significantly between males and females and between immature and mature red king crabs. Seasonal variations in the level of testosterone with the maximum value in the spawning period (May) indicate a potential role of the sex hormones in the maturation and reproduction processes of red king crab. Taking into account the slow growth rate in P. camtschaticus, our data could be useful not only for further physiological studies but also for the development of reliable techniques for red king crab aquaculture.

1. Introduction

The red king crab, Paralithodes camtschaticus (Tilesius, 1815), is a large commercially important species native to the North Pacific. A new self-sustaining population of this crab was reported to be established in the Barents Sea in the mid-1990s after its successful introduction by Russian specialists in the 1960s. Exponential population growth and range expansion of the crab has led to an increase in P. camtschaticus stock indices. Commercial fisheries for the red king crab were opened in 2002 in Norway and 2004 in Russia [1,2]. In Russian waters of the Barents Sea, annual landings of red king crab accounted for 9187 t in 2018, 9836 t in 2019 and 10,820 t in 2020 [3,4].
In the Barents Sea, different aspects of the red king crab biology and ecology have been intensively studied by marine scientists due to the invasive status of P. camtschaticus and its economic importance. Russian researchers have focused on distribution patterns, migration activity, molting and growth, reproduction, symbiotic relationships and effects on local benthic communities [2,4,5,6,7,8,9,10]. However, our knowledge of the physiology of this introduced species in its new environment is scarce, and information on biochemical profiles of red king crab is needed. Recently, we have reported concentrations of circulation ecdysteroids in hemolymph of P. camtschaticus [11]. Concentrations of a respiratory pigment, hemocyanin, were studied as a function of the meat content of commercial red king crabs from the Barents Sea [12].
The use of sex hormones and other hormones to regulate biological processes is a common strategy of vertebrate animals [13,14,15,16,17]. Usually, alterations in steroid hormone metabolism relate with effects on steroid hormone-dependent processes such as reproduction and growth [18]. Such alterations may be used as a biomarker for the effects of endocrine disruptors in invertebrates. Most stages of the steroidogenic pathways discovered for vertebrates have been demonstrated to occur in invertebrates. Although it was proposed that crustaceans do not actively synthesize vertebrate-type steroids in the same ways that echinoderms and mollusks do [19], the metabolism of these steroids was only investigated in a few crustaceans [18,20]. In crabs and lobsters, the endogenous precursor androstenedione is reduced to testosterone [21], while estrone is converted to estradiol [20]. Sex steroid-like substances can also be synthesized from cholesterol [22].
A high similarity was observed among the endocrine system of different crustaceans [23,24] and, therefore, sex hormones similar to those in vertebrates have been identified in several crustacean species including amphipods, shrimps, crayfish, lobsters, and crabs [19,25,26,27,28]. The presence of these hormones and their concentrations in red king crabs both in their native and non-native areas have not yet been reported. For this reason, the aim of our study was to measure concentrations of vertebrate-type sex hormones in hemolymph of the king crabs P. camtschaticus from the Barents Sea in relation to their sex and age.

2. Materials and Methods

Red king crabs were collected in August 2008 and May, July, and October 2009 in the coastal zone of the Barents Sea (Figure 1). The crabs were collected by divers at 5–40 m depths and using bottom traps at 50–60 m depths. Sex of each crab was determined visually. The crabs were weighed and their sizes were measured across the length of the carapace (CL, the greatest straight-line distance from the posterior margin of the right eye orbit to the medial-posterior margin of the carapace) [29]. All the crabs used for biochemical analyzes had new or old shells (2–24 months post ecdysis) [29]. Male crabs with CL < 90 mm were considered “immature,” whereas males with the CL > 90 mm were classified as “mature” according to Dvoretsky and Dvoretsky [8]. This separation is supported by the results of histological studies: in our samples the crabs smaller than 90 mm CL had no ripe spermatozoa in their testes in contrast to larger specimens. The same female groups were separated according to both histological data (immature females had oocyte diameter < 280 μm and white ovaries [5]) and size-at-maturity data (absence or presence of external eggs on their pleopods) [9]. In total, 23 immature (7 males and 16 females) and 33 mature (26 males and 7 females) crabs were analyzed.
After measuring the crabs, we sampled their hemolymph (0.6 mL) from the articulating membrane between the dactyl and propodus of the third walking leg using a sterile syringe with a needle, both washed with an anticoagulant containing EDTA and sodium citrate to prevent coagulation of the samples [29]. Each hemolymph sample was transferred to a sterile 2-mL plastic tube containing 1.4 mL of 96% ethanol. The samples were frozen and then transferred to the laboratory of the Institute of Physiology of Natural Adaptations (Arkhangelsk, Russia) for biochemical analyses.
Radioimmunoassays were carried out according to the protocols suggested by the manufacturer (A Beckman Coulter Company, Villepinte, France) using Immunotech RIA Testosterone or Immunotech RIA Estradiol test kits. In the case of testosterone, a 50-μL hemolymph sample and 500 μL of 125I-labelled testosterone were added serially to an antibody-coated tube. In the case of 17β-estradiol, a 100-μL hemolymph sample was used in the assays. A tube containing 500 μL of 125I-labelled testosterone (or estradiol) was included in every assay to determine the total 125I-activity (the sample “T”). The “testosterone” tubes were incubated at 37 °C in a waterbath for 3 h while the “estradiol” tubes were incubated with constant shaking (350 rpm) at ambient temperature for 3 h. At the end of incubation, the radioactivity of samples was determined using a scintillation counter (ARIAN, producer OOO VITAKO, Moscow, Russia). The standard graphs were plotted and the concentrations of testosterone and 17β-estradiol were obtained from the standard plot. The results were multiplied by a dilution factor of 3.33. The analytical sensitivity of the testosterone kit was 0.025 ng mL–1, the working RIA range was 0.025−20 ng mL–1, the coefficient of variation between samples was 14.8%. For the estradiol kit, these levels were <6 pg mL–1, 6−5000 pg mL–1 and 12.1%, respectively.
Carapace lengths and weight data in male and female red king crabs were compared using a one-way analysis of variance (ANOVA) or non-parametric Kruskal–Wallis tests in the case of non-normal data distribution. Since the sex hormone data were not normally distributed and failed testing for homogeneity of variances (modified Levene’s test, p < 0.05), testosterone and 17β-estradiol concentrations in relation to crab sex, crab size, and sampling season were compared using the Kruskal–Wallis test. When the test was significant, medians for different groups were compared using Bonferroni tests and differences were considered significant if p < 0.05. Statistical analyzes were carried out using STATISTICA (data analysis software system; http://www.statsoft.com/, accessed on 10 May 2020), version 6. Data are presented as means ± SE (standard error).
The taxonomic nomenclature follows the nomenclature according to WoRMS [30].

3. Results

Size and weight variations in red king crabs collected for the hemolymph sampling are presented in Figure 2.
Carapace length ranged from 49.0 to 162.7 mm, body weight—from 97 to 3805 g. Mean carapace length in immature male and female crabs was similar (Kruskal-Wallis test, df = 1, H = 0.090, p = 0.764). The same result was obtained for mature specimens (Kruskal-Wallis test, df = 1, H = 3.421, p = 0.064). Mean weight did not differ significantly between immature males and females (ANOVA, df = 1, F = 0.600, p = 0.447). Mature males were heavier than mature females (ANOVA, df = 1, F = 4.645, p = 0.039).
Biochemical assays have shown the presence of both testosterone and 17β-estradiol in the hemolymph of the crabs analyzed. Concentrations of testosterone varied from 0.08 to 1.39 ng mL–1 (mean for combined male and female data 0.46 ± 0.04 ng mL–1), while concentrations of 17β-estradiol ranged from 217.7–4100.1 pg mL–1 (1248.9 ± 91.4 pg mL–1) (Figure 3).
The comparisons of sex steroids in male and female red king crabs as well as in immature and mature specimens have shown that concentrations of both testosterone and 17β-estradiol were similar between all the combinations of the groups compared (Table 1). To increase the power of further analysis we used pooled data from males and females at different maturational stages in one complex. Seasonal variations in testosterone and 17β-estradiol concentrations are presented in Figure 4.
The mean level of testosterone decreased significantly from May to October whereas there was no significant difference detected among the seasonal concentrations of 17β-estradiol in the hemolymph samples (Table 1).

4. Discussion

According to our published [8] and unpublished size-at-age data, the age of the red king crabs used in this study varied from 3 to 11 years (females) and 3 to 13 years (males). The mean weight of large males was higher than that calculated for females because mature male red king crabs invest more energy in somatic growth in comparison to females, which invest the major proportion of their resources into reproduction processes [7,10].
Our study indicated that red king crabs have detectable concentrations of 17β-estradiol and testosterone in both male and female hemolymph. In general, the level of 17β-estradiol found for the female red king crabs was higher (Table 2) in comparison to females of some other decapod species such as Norwegian lobster Nephrops norvegicus in western Scotland [31], mud crabs Scylla serrata in India [32] and Scylla paramamosain in China [27], Chinese mitten crab Eriocheir sinensis in China [33], edible crab Spiralothelphusa senex (cited as Oziothelphusa senex senex) in India [34], soldier crab Mictyris brevidactylus in northern Taiwan [35] and grass shrimp Pandalus kessleri in Japan [25].
The estradiol concentration registered in the red king crab male hemolymph was higher than in Eriocheir sinensis males [33], while the male testosterone level was comparable to the concentration reported for the hemolymph of S. paramamosain [27]. In the red king crabs, the levels of both hormones were much higher than in gammarid amphipods Gammarus duebeni celticus and G. pulex in Northern Ireland and G. pseudolimnaeus in Waukesha County, WI, USA [28]. It is difficult to evaluate causes responsible for this result, but most likely the higher concentrations of sex hormones in the red king crab hemolymph were associated with their larger size and weight. For example, the mud crabs S. paramamosain used in the study described by Huiyang et al. [27] had a body length of 36–87 mm, while the average weight of mature Spiralothelphusa senex females used for biochemical assays in the study by Swetha et al. [34] was 32–37 g. Additionally, the largest CL reported for adult female Nephrops norvegicus is about 50 mm CL [41]; females of Scylla serrata attain sexual maturity after reaching 80 mm carapace width (CW) [42], and females of Eriocheir sinensis become mature at 34.1 ± 3.9 mm CL with a weight of 26.6 ± 8.1 g [43]. The largest adult females of Mictyris brevidactylus belong to a size class of 110–120 mm CW [44]. The majority of the mentioned crustaceans occur in temperate and warm waters whereas the red king crabs live in a cold-water environment. Different habitats may also contribute to differences between the levels of sex hormones in P. camtschaticus and those crustacean species.
In vertebrates, both males and females produce testosterone and 17β-estradiol, although the concentrations of these hormones may vary significantly depending on sex and the reproductive cycle [28].
Taking into account the differences in invertebrate and vertebrate endocrine systems, there was no reason to assume that typical sex-specific differences in sex hormones among vertebrates would also be found in red king crabs. Our data support to some extent this assumption: we found no significant differences in testosterone and 17β-estradiol concentrations in relation to age and sex of the red king crabs. Similar results were reported by other authors. For example, males of Gammarus duebeni celticus, G. pulex, and G. pseudolimnaeus had comparable concentrations of 17β-estradiol, and females of these species had comparable concentrations of testosterone [28].
On the other hand, the ovaries of some decapods may synthesize 17β-estradiol and release this hormone into the hemolymph, and then it may reach the hepatopancreas to stimulate vitellogenin synthesis [26]. For this reason, concentrations of sex steroids in gonads, eggs, and hepatopancreas of crustaceans are higher than in their hemolymph (Table 2). Thus, an association between sex hormone profiles and stages of vitellogenesis was detected in some decapod species [45]. For example, the levels of 17β-estradiol increased significantly in the tissues of crabs Scylla serrata, S. paramamosain, and Spiralothelphusa senex during late vitellogenesis [27,32,34]. Similar trends were reported for testosterone as well [27]. In addition, concentrations of sex hormones were found to positively correlate with the reproductive status of decapod crustaceans, as they were high during the pre-reproductive season and low during the non-reproductive season [35,37,46]. We also found seasonal changes in the testosterone profile assayed in the Barents Sea red king crabs. The maximum (0.8 ng mL–1) was registered in May and the minimum (0.2 ng mL–1) in October. Spawning season in P. camtschaticus lasts from February to May with a peak in April [5]. Thus, we expected to find the highest level of testosterone in the May samples of adult crabs. We found no seasonal fluctuations in the 17β-estradiol concentration. This result could be explained by the fact that we studied hemolymph, whereas estrogens are synthesized in the ovaries of red king crabs. These organs are much heavier than the male testes. Monthly variations of testosterone in immature crabs more likely reflected seasonal patterns of P. camtschaticus maturation in the Barents Sea.
The effects of 17β-estradiol on vitellogenesis (vitellogenin synthesis, oocyte development, an increase of ovarian indices, and growth rates) have been shown for the kuruma prawn Marsupenaeus japonicus [47], giant freshwater prawn Macrobrachium rosenbergii [48], freshwater crayfish Cherax albidus [49], burrowing crab Chasmagnathus grdnulata [50], and lobsters Homarus americanus and Panulirus homarus [51]. In addition, Nagabhushanam and Kulkarni [52] showed that exogenous testosterone can stimulate testicular development in the marine penaeid prawn, Mierspenaeopsis hardwickii (cited as Parapenaeopsis hardwickii). This hormone also induced sperm development and subsequent mating success in male tiger shrimps Penaeus monodon [53]. In contrast, the results by Okumura and Sakiyama [38] suggested that 17β-estradiol and testosterone did not play an important role in ovarian development in Penaeus japonicus (cited as Marsupenaeus japonicus), and Koskela et al. [54] reported no effect 17β-estradiol on development and reproduction of the tiger prawn Penaeus esculentus.
In the last several decades, aquaculture has grown rapidly in complexity and in volume around the world. The majority of aquaculture businesses require substantial amounts of both operating and investment capital. For this reason, profitable aquaculture cannot be organized without excellent knowledge on the biology and ecology of target species [55,56,57]. The development of specific methods to increase growth rates of slow-growing species such as red king crab is a great challenge for modern science [58,59], and our results may have important implications for further studies focused on aquaculture of P. camtschaticus.

5. Conclusions

Because molting and reproduction in crustaceans are controlled both by ecdysteroids (molting hormones) and vertebrate-like steroids, these hormones are considered as potential inductors of growth and maturation processes in cultured crustaceans. Understanding the controlling mechanisms of reproductive processes and molting in red king crabs is an important issue because of the slow growth rate of this species (the commercial size of 150 mm CW is reached at 10 years). Thus, the determination of the sex steroid levels in the red king crab Paralithodes camtschaticus is a first step toward developing new aquaculture techniques. The level of testosterone/17β-estradiol varied from 0.08–1.39 ng mL–1/217.7–2703.2 pg mL–1 in males and from 0.12–1.29 ng mL–1/335.6–4100.1 pg mL–1 in females. Further studies should reveal the possibility of the use of artificially synthesized hormonal preparations for accelerating the maturation process in red king crabs and, consequently, increasing their growth rates under laboratory conditions. Such studies will provide a baseline for the effective planning of regulatory measures and aquaculture programs in the Barents Sea region.

Author Contributions

Conceptualization, A.G.D. and E.V.T.; data curation, A.G.D., A.E.E., V.A.A., and V.G.D.; validation, formal analysis, A.G.D., E.V.T., V.G.D., A.E.E. and V.A.A., funding acquisition, A.G.D. and E.V.T.; methodology, E.V.T.; software, visualization, V.G.D., project administration, A.G.D.; writing—original draft, A.G.D. and V.G.D.; writing—review and editing, A.G.D., V.G.D. and E.V.T. All authors have read and agreed to the published version of the manuscript.

Funding

This article is based upon work that was supported by the Ministry of Science and Higher Education of the Russian Federation under projects AAAA-A19-119011690138-0 for MMBI RAS and AAAA-A19-119120990060-0 for FECIAR UrB RAS.

Institutional Review Board Statement

This study was carried out in accordance with Russian legislation guidelines (Federal Act 52-F3, 24/04/1995) and approved by the Institutional Review of Murmansk Marine Biological Institute (6732/253-ok, 01/12/2016).

Data Availability Statement

Data will be made available upon any reasonable request to the corresponding author.

Conflicts of Interest

The authors declare no conflict of interest.

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Animals 11 02149 g001 550
Figure 1. Study area in the southern Barents Sea.
Figure 1. Study area in the southern Barents Sea.
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Animals 11 02149 g002 550
Figure 2. Carapace length and weight variations in the Barents Sea red king crabs analyzed for sex hormones.
Figure 2. Carapace length and weight variations in the Barents Sea red king crabs analyzed for sex hormones.
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Animals 11 02149 g003 550
Figure 3. Variations of sex hormones in immature and mature red king crabs from the coastal zone of the Barents Sea. Green and red circles are outliers.
Figure 3. Variations of sex hormones in immature and mature red king crabs from the coastal zone of the Barents Sea. Green and red circles are outliers.
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Animals 11 02149 g004 550
Figure 4. Seasonal variations in vertebrate-type sex hormones in hemolymph of red king crabs from the Barents Sea. Green circles are outliers. Bars with the same letter are not significantly different (p > 0.05).
Figure 4. Seasonal variations in vertebrate-type sex hormones in hemolymph of red king crabs from the Barents Sea. Green circles are outliers. Bars with the same letter are not significantly different (p > 0.05).
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Table
Table 1. Results of Kruskal–Wallis tests comparing the differences in sex hormone levels of red king crabs.
Table 1. Results of Kruskal–Wallis tests comparing the differences in sex hormone levels of red king crabs.
HormoneComparisonsdHp
TestosteroneM-im vs. M-mat10.4360.509
F-im vs. F-mat10.8750.349
M-tot vs. F-tot10.7500.386
May vs. July vs. August vs. October324.0300.00002
17β-estradiolM-im vs. M-mat10.0010.982
F-im vs. F-mat10.6980.404
M-tot vs. F-tot11.0320.310
May vs. July vs. August vs. October30.9500.813
Note. M—male, F- female, im—immature, mat—mature, tot—total, d—degree of freedom, H—chi-square level, p—probability level.
Table
Table 2. Concentrations of vertebrate-like sex steroids identified in various crustacean species.
Table 2. Concentrations of vertebrate-like sex steroids identified in various crustacean species.
SteroidSpeciesSexMatrixLevelsReference
ENephrops norvegicusFEggs900 pg g–1[31]
ENephrops norvegicusFHemolymph800 pg mL–1[31]
EScylla serrataFHemolymph230–1040 pg g–1[32]
EScylla serrataFOvary180–1250 pg g–1[32]
EScylla serrataFHepatopancreas300–4100 pg mg–1[32]
EScylla olivaceaFHemolymph970–3520 pg mL–1[36]
EPandalus latirostrisFHemolymph18.1–54.3 pg mL–1[25]
EPenaeus monodonFHemolymph30.4 pg mL–1[37]
EPenaeus monodonFOvary30–77 pg g–1[37]
EPenaeus monodonFHepatopancreas20–752.6 pg mg–1[37]
EPenaeus japonicusFHemolymph2.8–8.7 pg mL–1[38]
EGammarus duebeniFHemolymph86.6 pg mL–1[28]
EGammarus duebeniMHemolymph41.6 pg mL–1[28]
EGammarus pulexFHemolymph38.8 pg mL–1[28]
EGammarus pulexMHemolymph47.4 pg mL–1[28]
EGammarus pseudolimnaeusFHemolymph18.8 pg mL–1[28]
EGammarus pseudolimnaeusMHemolymph29.3 pg mL–1[28]
EScylla paramamosainFHemolymph18.5–75.4 pg mL–1[27]
EEmertia emeritusFOvary2000–8000 pg g–1[26]
EEmertia emeritusFHepatopancreas2900–9700 pg g–1[26]
EMacrobrachium rosenbergiiFOvary67–341 pg g–1[26]
EMacrobrachium rosenbergiiFHepatopancreas168–663 pg g–1[26]
EEriocheir sinensisFHemolymph118.8–291.8 pg mL–1[33]
EEriocheir sinensisFOvary232.2–257.8 pg g–1[33]
EEriocheir sinensisMHemolymph122.7–237.6 pg mL–1[33]
EEriocheir sinensisMTestes128.5–150.0 pg g–1[33]
ESpiralothelphusa senexFHemolymph27.9–134.2 pg mL–1[34]
EMictyris brevidactylusFHemolymph0.2–0.6 pg g–1[35]
EMictyris brevidactylusFOvary8.8–70.0 pg g–1[35]
EMictyris brevidactylusFHepatopancreas0.6–122.9 pg g–1[35]
TNephrops norvegicusFOvary19000 pg g–1[31]
THomarus americanusMTestes14300 pg g–1[39]
TGammarus duebeniFHemolymph25.3 pg mL–1[28]
TGammarus duebeniMHemolymph15.6 pg mL–1[28]
TGammarus pulexFHemolymph22.1 pg mL–1[28]
TGammarus pulexMHemolymph22.7 pg mL–1[28]
TGammarus pseudolimnaeusFHemolymph21.7 pg mL–1[28]
TGammarus pseudolimnaeusMHemolymph31.4 pg mL–1[28]
TScylla paramamosainMHemolymph394–607 pg mL–1[27]
TPenaeus japonicusFHemolymph2.2–4.4 pg mL–1[38]
TNeocaridina denticulataNDHemolymph2700 pg g–1[40]
Note: M—male, F—female, ND—no data, E—17β-estradiol, T—testosterone.
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Dvoretsky, A.G.; Tipisova, E.V.; Elfimova, A.E.; Alikina, V.A.; Dvoretsky, V.G. Sex Hormones in Hemolymph of Red King Crabs from the Barents Sea. Animals 2021, 11, 2149. https://doi.org/10.3390/ani11072149

AMA Style

Dvoretsky AG, Tipisova EV, Elfimova AE, Alikina VA, Dvoretsky VG. Sex Hormones in Hemolymph of Red King Crabs from the Barents Sea. Animals. 2021; 11(7):2149. https://doi.org/10.3390/ani11072149

Chicago/Turabian Style

Dvoretsky, Alexander G., Elena V. Tipisova, Aleksandra E. Elfimova, Viktoria A. Alikina, and Vladimir G. Dvoretsky. 2021. "Sex Hormones in Hemolymph of Red King Crabs from the Barents Sea" Animals 11, no. 7: 2149. https://doi.org/10.3390/ani11072149

APA Style

Dvoretsky, A. G., Tipisova, E. V., Elfimova, A. E., Alikina, V. A., & Dvoretsky, V. G. (2021). Sex Hormones in Hemolymph of Red King Crabs from the Barents Sea. Animals, 11(7), 2149. https://doi.org/10.3390/ani11072149

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