- 1Heilongjiang River Fisheries Research Institute, Chinese Academy of Fisheries Sciences, Harbin, China
- 2Scientific Observing and Experimental Station of Fishery Resources and Environment in Heilongjiang River Basin, Ministry of Agriculture and Rural Affairs, Harbin, China
- 3Yingkou Enrichment Experiment Station, China Academy of Fisheries Science, Yingkou, China
- 4College of Marine Science, Technology and Environment, Dalian Ocean University, Dalian, China
The stability of the ecosystem directly affects the water quality and safety, fishery production, and people’s quality of life along the route. In this study, extensive biological information on five dominant species of prey fish, including Hemiculter leucisculus (Basilewsky, 1855), Acheilognathus macropterus (Bleeker), Rhodeus sericeus (Pallas,1776), Pseudorasbora parva (Temminck & Schlegel, 1846), and Squalidus argentatus (Sauvage & Dabry de Thiersant, 1874), was collected in the lower reaches of the Songhua River, and the population parameters and variation rules of these fish were evaluated. The results showed that at present, the fish resources in the lower reaches of the Songhua River were in an overexploited state. Although the growth rate of prey fish was accelerating, their growth potential was decreasing. In addition to the homogeneous structure of the fish community, it was increasingly evident that a high proportion of small-sized fish were present in the fish community. In addition, the growth length coefficients of the five prey fish species were all greater than 0.2, indicating that the prey fish were growing at a faster rate, and the range of the growth performance indicators were 3.49 ~ 4.37. Our data also demonstrated that the exploitation rates of Hemiculter leucisculus and Squalidus argentatus were both greater than 0.5, and the exploitation rates of all species were higher than Emax except for Pseudorasbora parva. Finally, based on the above results, the mesh size of all nets should be controlled above 45 mm to ensure the size of the main prey fish populations in the lower reaches of the Songhua River. In summary, these results provided variation rules and growth of prey fish resources in the lower reaches of the Songhua River. At the same time, the distribution of major commercial or endangered baiting grounds in the lower reaches of the Songhua River was determined, which was beneficial to the balance and integrity of the ecosystem.
1 Introduction
The Songhua River, located in the northeastern part of China, is one of the seven major river basins in China. The northern source of the Songhua River originates from the Nengjiang River in the Yilehuli Mountains, a branch of the Daxinganling Mountains, and the southern source originates from the west-flowing Songhua River in the Changbai Mountains, which converges into the main channel of the Songhua River in Zhaoyuan County, Daqing (Yu et al., 2018). The river basin covers an area of about 55.7 × 104 square kilometers (Lu et al., 2022). As the mother river of Heilongjiang and Jilin provinces, the extensive basin and special geographical environment of the Songhua River have created their own rich fish resources. Since the 1930s, fish surveys have been conducted successively on the Songhua River (Yang et al., 2015). However, with the development of agriculture and industry and the increase of population, the fish resources of the Songhua River are greatly challenged by illegal anthropogenic fishing practices such as electrofishing and over-small nets. In addition, the construction of hydroelectric power stations and dams along the Songhua River has resulted in changes to the river and watershed (Han et al., 2017; Ma et al., 2022), seriously damaging the “three grounds and one channel” (overwintering ground, baiting ground, spawning ground, and migration channel) for local fish, and threatening the water quality and safety, environmental carrying capacity, and fishery resources of the Songhua River.
At present, studies on the Songhua River are focused on fish toxicology (Liu et al., 2009; Wang and Wang, 2019), community structure analysis (Li et al., 2018), early fish resource research (Yang et al., 2019), economic fish biology (Wang et al., 2020; Wang et al., 2021), resource variability (Lu et al., 2021), and behavioral observations (Li et al., 2021); whereas little research has been conducted on prey fish in the Songhua River. In addition, a significant portion of prey fish such as Hemiculter leucisculus and Acheilognathus macropterus in the Songhua River are omnivorous. Therefore, as the main food source for medium and large commercial and endangered fish, prey fish is a key element of primary productivity in the ecosystem, and their population size and variation affect the community structure of commercial fish as well as fish in the entire ecosystem. However, compared with other large and medium-sized fish, prey fish have limitations such as low economic value and low social impact, which directly lead to little research on prey fish and incomplete understanding the current status of exploitation of prey fish resources. In addition, under the current high-intensity commercial fishing operations, an urgent issue to be addressed is how to ensure the sustainable development of prey fish population resources and the stability of fish community structure in the Songhua River.
Therefore, the prey fish in the lower reaches of the Songhua River was taken as the research object in this study. The dynamic of population were studied, and fish community structure in the lower reaches of the Songhua River was determined. Meanwhile, based on the research results, reasonable fishing management policies are proposed to provide a reasonable reference for the development of relevant fisheries management measures and provide a scientific basis for the sustainable development of the Songhua River and the stability of the ecosystem.
2 Materials and methods
2.1 Sample collection and identification
Samples were collected from the river sections of the Songhua River in Tangyuan County, Huachuan County, Fujin City and Tongjiang City. The sampling sites are shown in Figure 1, which was drawn using ArcGis 10.5 software. Samples for each site were collected in the summer (June–July), autumn (October–November), and winter (December) in 2020 as well as in the spring (May) and summer (July–August) in 2021. Gill nets and ground cages were used for sample collection. Each gill net was 20,000 cm long and 250 cm high with dimensions of 1 cm, 2 cm, 4 cm, 6 cm, 8 cm, and 10 cm, respectively. The ground cages were 1500 cm long, 40 cm wide and 40 cm high with dimensions of 0.5 cm. The size of the net was measured by straightening the opposite knot. Sampling was conducted in accordance with the related reference (Zhang, 1995; Xie, 2007; Zhao, 2018). The sampling specifications such as measurement records and anatomy of samples were in accordance with the relevant manuals and specifications of the Inland Fisheries Natural Resources Survey (Zhang, 1991).
Figure 1 Sampling area. TY, Tangyuan county; HC, Huachuan county; FJ, Fujin city; TJ, Tongjiang city.
2.2 Data analysis and processing
2.2.1 Sample analysis and dominant species identification
Based on the results of catch collection during the survey, the dominant species were identified using the relative importance index (IRI) method. The IRI is calculated as follows:
where N is the proportion of the number of a certain species to the total catch, is the proportion of the mass of a species to the total catch, and is the frequency of a certain species. The IRI of each catch species was in the range of [0, 1), [1, 10), [10, 100), [100, 1000), and [1000, +∞), representing rare, ordinary, common, important, and dominant species, respectively (Pauly and Munro, 1984; Thangaraj et al., 2022). Considering the actual situation of the Songhua River, five prey fish with IRI index greater than 200 were selected as the objects of this study.
2.2.2 Basic growth characteristics and parameters
The relationship between the body length-weight coefficients of target fish in the lower reaches of the Songhua River conforms to the power function curve (Fei, 1990). To establish the length-weight relationship, the existent equations were applied (Ricker, 1975; Quinn and Deriso, 1999), and the body length-weight relationship is calculated as follows:
where W is body weight (g), L is body length (mm), a is a condition factor for growth, and b is a power exponent coefficient. Based on the principle of least squares, the values of parameters a and b can be estimated by using the linear regression of the logarithm of body weight on the logarithm of body length.
The von Bertalanffy growth formula (VBGF) was fitted to estimates of the length-at-age curve using non-linear least-squares estimation procedures (Pauly et al., 1992). The VBGF is defined by the equation:
where is the theoretical length at age t, is the asymptotic length of the sample, k is the average curvature of the sample growth curve (relative rate of convergence to the asymptotic value), t is the age of the sample, and is the theoretical initial age at which the length is zero (Pauly and David, 1981; Newman, 2002). and k of the VBGF were estimated by means of ELEFAN I in the FISAT II computer program (Pauly, 1981; Pauly, 1982). of target fish in the lower reaches of the Songhua River was calculated ac cording to an empirical formula by Pauly and David (1981).
The estimates of and k were used to estimate the growth performance indices ( and growth inflection point age () (Pauly and Munro, 1984) using the following equations:
2.2.3 Death, development and survival parameters
The total instantaneous mortality (Z) was estimated using the body length converted catch curve method in the FiSAT II computer program (Pauly, 1983; Pauly, 1984; Pauly, 1990), which is expressed as follows:
where is the number of mortalities in this population N at instant t and b is a parameter.
The instantaneous rate of natural mortality (M) was obtained using the empirical relationship of Pauly (Pauly, 1980), which is expressed as follows:
where T is the annual habitat temperature (°C) of the water in which the stocks live.
Once Z and M had been obtained, the instantaneous rate of fishing mortality (F), exploitation rate (E) (Guo et al., 2016), and survival rate (S) were represented by the relationship between the three transient mortality rates according to a previous study by the authors (Yin et al., 2016):
The critical age of the population (tcr) is the age at which the instantaneous rate of natural mortality of an individual is the same as the relative growth rate of its body weight, or when the biomass of a generational population of fishery organisms reaches its maximum. This could be expressed as follows:
2.2.4 Survival probability estimation
The length-based Bayesian biomass (LBB) method in the FISAT II computer program was chosen for survival probability estimation of target fish in the lower reaches of the Songhua River. Some numerical values were taken from the Markov chain Monte Carlo equation (MCMC) (Froese et al., 2018), which is expressed as follows:
where Lstart is the minimum body length of the target fish stock to be caught, which is considered as the opening trap body length, and NL is the number of surviving individuals of length L caught in the target fish population.
Under the premise of no commercial fishing operations, there is no information about the magnitude of the variables in the formula. Therefore, mathematical statistics can be directly used to calculate the survival rate of individuals with body length L for the target fish population in the lower reaches of the Songhua River when F = 0 (Wang et al., 2020), as follows:
2.2.5 Catch per unit of replenishment
The relative yield per recruit (Y’/R) was analyzed through the improved Beverton-Holt (B-H) dynamic equation (Pauly and Soriano, 1986; Gayanilo et al., 2005), which is expressed as follows:
where Lc is the opening catch length of target fish, and E is the exploitation rate.
3 Results
3.1 Catch statistics
A total of 21,520 fish, with a total weight of 2,833,900.85 g, belonging to 60 species of fish in 7 orders and 14 families were collected in this study (Table 1). Among them, the dominant prey fish were Hemiculter leucisculus, Acheilognathus macropterus, and Pseudorasbora parva, and the common prey fish were Squalidus argentatus, Rhodeus sericeus, Gobio cymocephalus (Dybowsky,1869), and seven other species. To investigate the population status of major prey fish in the lower reaches of the Songhua River, the top five categories in the IRI index were selected for this study.
3.2 Basic growth characteristics of prey fish
According to the basic growth characteristics of the captured 3259 target samples, including 1258 Hemiculter leucisculus, 772 Acheilognathus macropterus, 347 Rhodeus sericeus, 483 Pseudorasbora parva, and 399 Squalidus argentatus, the frequency distribution of length frequency distribution, length-weight relationship (Supplementary Figures 1, 2), and the growth characteristics of prey fish were obtained. As shown in Table 2, the b-values of Hemiculter leucisculus, Acheilognathus macropterus, Rhodeus sericeus, Pseudorasbora parva, and Squalidus argentatus were 3.0083, 3.2031, 2.8775, 2.9773, and 2.9603, respectively. In terms of , all five prey fish were between 3.4 and 4.4. Hemiculter leucisculus ( = 4.37) had the highest growth performance index, while Rhodeus sericeus ( = 3.49) was the lowest. The growth equation could be fully expressed based on the length frequency distribution using the VBGF. The asymptotic length of Hemiculter leucisculus was 198.2 mm, which was different from other fish. The asymptotic lengths of other fish were all around 100 mm. Among them, Squalidus argentatus had the smallest asymptotic length of 89.25 mm. In terms of growth rate, the k-value of Rhodeus sericeus was lower than that of the other fish, although all the fish belonged to the same fast-growing species.
3.3 Prey fish population parameters
The population parameters of major prey fish in the lower reaches of the Songhua River were obtained from length frequency relationship. As presented in Figure 2, the Z of Hemiculter leucisculus, Acheilognathus macropterus, Rhodeus sericeus, Pseudorasbora parva, and Squalidus argentatus was 1.98, 2.17, 1.16, 2.33, and 3.13, respectively. The water temperature T was 12°C based on our year-round monitoring in the target waters. The M, F, S, E, and tcr of the target fish could be further obtained in Table 3.
Figure 2 Length-converted catch curves of (A) Hemiculter leucisculus, (B) Acheilognathus macropterus, (C) Rhodeus sericeus, (D) Pseudorasbora parva, and (E) Squalidus argentatus in the lower reaches of the Songhua River. The slope of each straight line is the total instantaneous mortality rate (Z) of the target fish population.
3.4 Status of prey fish resources in the lower Songhua River and management strategies
As shown in Table 1, the proportions of medium- and large-sized fish were small at this stage. On the contrary, the dominant and common species were mostly small- and medium-sized prey fish. Therefore, it was reasonable to conclude that the current fishing pressure in the lower reaches of the Songhua River and the small mesh sizes used had resulted in a continuous increase in the fishing yield of prey fish that were originally caught as bycatch. In addition, the opening length (Lc) of the target prey fish, including Hemiculter leucisculus (40 mm), Acheilognathus macropterus (30 mm), Rhodeus sericeus (20 mm), Pseudorasbora parva (20 mm), and Squalidus argentatus (25 mm) could be inferred based on the results of fishing gear in the target waters. Currently, the opening catch length is known, so samples with body lengths smaller than the opening catch length are identified as a supplemental population. Taking Hemiculter leucisculus as an example, with the increase in fishing intensity, biomass () loss gradually increases and yield () first increases and then decreases, with the inflection point being Emax (Figure 3). The exploitation rates, including E0.1, E50%, and Emax of the target prey fish were obtained by the knife-edge selection hypothesis in the (B-H) dynamic equation (Table 3). The dynamic change trend between the yield per unit replenishment, Lc and E was estimated as shown in Figure 4. When the fishing intensity is constant, Lc decreases, increases and then decreases, and the point of inflection is ELopt.In the current fishing mode, the values of and were 0.20 and 0.51, respectively. Similarly, the values of and values for other fish species are detailed in Table 3.
Figure 4 Relationship between relative yield per recruit Y′/R, exploitation ratio, and catchable size of Hemiculter leucisculus. The point a represents the Y′/R value in the current state. The point b represents the maximum Y′/R value when changing the body length of different start catches in the current exploitation state. Each loop in this figure is the equivalent of the Y’/R value. It means that the Y’/R values of the same loop are equal for the same starting catch length, different exploitation states or different starting catch lengths in the same exploitation state. The redder the color, the higher the Y’/R value, and conversely, the bluer the color, the lower the Y’/R value.
4 Discussion
4.1 Changes in major commercial fish species in the lower reaches of the Songhua River
The Songhua River in the Three Rivers Plain has an irreplaceable ecological status due to its unique geographical location and extensive watershed. Therefore, fish resource surveys on the lower reaches of the Songhua River have been conducted since 1950. First, in terms of fish community structure in the lower Songhua River, previous studies had recorded a total of 98 species of fish in the Songhua River basin, including 10 orders, 20 families, and 68 genera, of which a total of 80 species (including subspecies), including 9 orders and 19 families and 60 genera, were collected in the lower reaches (Yang et al., 2015). In the latest study, 60 species of fishes were collected from the lower reaches of the Songhua River, including 7 orders and 14 families, with 20 fewer species than in the previous study. Second, according to the fishery resources survey report of the Songhua River system, the catches of Gyprinus carpio (Linnaeus, 1758) and Parabramis pekinensis (Basilewsky, 1855) tended to accounted for about 60% of the total annual catches, followed by the Culter ilishaeformis (Basilewsky, 1855) (10% on average), Hypophthalmichthys molitrix (Valenciennes, 1844) (10% on average) and Ctenopharyngodon idella (Valenciennes, 1844) (5% on average) around the 1960s. In addition, Oncorhynchus keta (Walbaum, 1792), Amur sturgeon (Brandt, 1869), Kaluga sturgeon (Georgi, 1775), Hucho taimen (Pallas, 1773), and Brachymystax lenok (Pallas, 1773) also occupied a certain proportion of the total annual catches. After the 1980s, the commercial fish that caught in production amounts were changed to Gyprinus carpio, Carassius auratus (Linnaeus, 1758), Silurus asotus (Linnaeus, 1758), Hypophthalmichthys molitrix, Aristichthys nobilis (Richardson, 1845), Ctenopharyngodon idella, and Hemibarbus maculatus (Bleeker, 1871) (Wei, 2018). In addition, the proportion of fish began to change, with Culter ilishaeformis becoming the most productive fish, accounting for about 60% of the total production. Gyprinus carpio production dropped from about 60% to about 10%, followed by Parabramis pekinensis (Basilewsky, 1855) (about 12.5%) and Hypophthalmichthys molitrix (about 7.6%). According to our survey results in 2015, the dominant and common species in the lower reaches of the Songhua River were Gyprinus carpio, Hypophthalmichthys molitrix, Silurus asotus, Carassius auratus, Hemiculter leucisculus, Xenocypris argentea (Günther, 1868), Pelteobagrus nitidus (Sauvage et Dabry, 1874), Parabramis pekinensis, and Hemibarbus maculatus. Compared to the present results, most of these fish were of relatively high economic value. In addition, growth characteristics and populations of the same species of fish changed over time and space. It has been reported showed that Carassius auratus, Gyprinus carpio, Hemiculter leucisculus, Leuciscus waleckii (Dybowski, 1869), and Cultrichthys erythropterus (Cultrichthys erythropterus) were the dominant species in the lower reaches of the Songhua River in 2012 (Yang et al., 2015). In the past 10 years, the growth rate of Hemiculter leucisculus changed from moderate to rapid, accompanied by a decrease in growth potential and survival rate (Table 4). In fact, anthropogenic factors such as construction of water-related projects, disturbance of agroforestry industries and increased intensity of commercial fishing have led to changes in the dominant fish from large and medium-sized and commercially valuable fish to small and low-value fish.
Table 4 Comparison of growth characteristics and population change parameters of the Hemiculter leucisculus population in the lower reaches of the Songhua River over 10 years.
4.2 Prey fish resource management strategy in the lower reaches of the Songhua River
As a secondary productivity of the ecosystem, changes in prey fish populations have profound effects on fish at the higher trophic levels of the food chain, including endangered fish such as Acipenser schrencki (Li et al., 2020), Hucho taimen, Coregonus ussuriensis (Bochkarev et al., 2017), and medium and large fish with high economic value such as Channa argus (Liu et al., 2000) and Silurus asotus (Jiang et al., 2022). With the increase in current commercial fishing intensity and the reduction in mesh size, the former bycatch of prey fish has gradually become the target of fishing and made into fishmeal for profit. Gulland (1989) indicated that the optimal exploitation intensity should be 0.5. In addition, Mehanna (2007) suggested that the population is in a safe state of exploitation when the exploitation intensity is not higher than Emax. However, our results demonstrated that Hemiculter leucisculus and Squalidus argentatus were in an overexploited state. Pauly also suggested that the optimal exploitation point should be 0.286 (Pauly, 1987), where all resources are in a state of overexploitation. Based on the results of the population parameters and the values fitted for different exploitation states, the E50% for all five prey fish species in the current exploitation state was close to the optimal value (Table 5). To ensure biomass loss below 75%, the catch with ELopt is the largest, and the manipulation of adjusting the fishing size is much less difficult than setting the exploitation intensity. Therefore, the optimal management specifications for the Hemiculter leucisculus, Acheilognathus macropterus, Rhodeus sericeus, Pseudorasbora parva, and Squalidus argentatus population were defined as 101.08, 55.93, 43.58, 42.89, and 44.63 mm, respectively. Based on these estimates, it is possible to determine the minimum mesh size to be used in the lower reaches of the Songhua River. Considering convenience of operation, the mesh specifications could be controlled above 45 mm. However, when the opening and catching specifications are controlled at 45 mm, the above results will not be materially affected by the confirmatory calculation. Especially considering the small changes in the catch and the biomass loss of Hemiculter leucisculus and Acheilognathus macropterus populations at this stage, it is recommended that the mesh size of all nets in the lower reaches of the Songhua River should be controlled at 45 mm or greater.
4.3 Upstream effects of prey fish in the lower reaches of the Songhua River
The upward effect is a “bottom-up” effect, where the quantities of resources and biomass at lower trophic levels determine the population structure at higher trophic levels (Ware and Thomson, 2005; Buchheister et al., 2015; Maitra et al., 2018). Therefore, it is reasonable to assume that the population size and variation patterns of prey fish play a key role in the recovery and rebuilding of their predator populations. From a feeding perspective, most species have similar feeding habits to their juvenile predators, leading to the formation of a competitive relationship for feeding. Therefore, when small-sized fish proliferate uncontrollably, this will have a greater impact on their predator populations, thereby affecting the rationality of the fish community structure and ultimately the balance of the entire ecosystem. Similarly, the feeding habits of prey fish are close to those of the juvenile fish of their predators, thus forming another competitive relationship (Sharp, 2001). A previous study has proved that a decline in jellyfish-feeding fish resources caused an increase in the number of jellyfish species, which instead led to a decrease in the number of juvenile fish in the East Sea and Yellow Sea of China (Greve, 1994). As a representative of large economic fish and endangered fish, Huso dauricus (Georgi, 1775) in the Songhua River, for example, its egg stage is also a food source for other fish (including some other prey fish).The juvenile stage of Huso dauricus (before 1 year of age) is in competition with other prey fish, such as Hemiculter leucisculus. Hemiculter leucisculus and Squalidus argentatus are the main baits for adult Huso dauricus. Therefore, the upward effect triggered by the population size of prey fish in the Songhua River had a direct impact on zoophagous commercial fish and endangered fish.
In addition to the upstream effect of prey fish, there are also factors affecting the community structure of their predatory fish, such as the physical and chemical environment of the habitat waters themselves, human intervention, and commercial fishing. A previous study showed that Hemiculter leucisculus, Parabotia fasciatus, Saurogobio dabryi, and Rostrogobio amurensis were the dominant species among the drifting eggs and juvenile fry in the lower reaches of the Songhua River in recent years (Huo et al., 2022). Therefore, the number of prey fish can be expected to remain dominant in the coming years.
5 Conclusion
Currently, the fish resources in the lower reaches of the Songhua River are in a state of high intensity exploitation. Unless effective management measures are taken in time, the structure of the fish community in the lower Songhua River will gradually homogenize, the fish individuals will become smaller and younger, causing the reduction of fishery resources in the Songhua River basin. Therefore, all mesh sizes should be controlled above 45 mm in accordance with the above management strategy to control the size of prey fish populations. At the same time, the authorities and local people need to reduce the frequency of commercial fishing boat operations and the use of banned nets. In addition, the construction of water-related projects and sewage discharge should be reduced to ensure the survival space of commercial fish, which will be beneficial to restore the balance and integrity of the Songhua River ecosystem.
Data availability statement
The original contributions presented in the study are included in the article/Supplementary Material. Further inquiries can be directed to the corresponding author.
Ethics statement
The animal study was reviewed and approved by the Committee for the Welfare and Ethics of Laboratory Animals of Heilongjiang River Fisheries Research Institute of Chinese Academy of Fishery Sciences.
Author contributions
WL: Methodology, Formal analysis, Visualization, Writing - original draft. PL: Investigation. BM: Validation. TH: Data curation. FT: Conceptualization, Writing - review and editing. ZY: Software, Writing - review and editing. JW Funding acquisition and Supervision. All authors contributed to the article and approved the submitted version.
Funding
The research was financially supported by the Special project on agricultural financial fund from the Ministry of Agriculture and Rural Affairs of China entiled “Survey of fishery resources and environment in key waters of Northeast China” and Central Public-interest Scientific Institution Basal Research Fund (No. 2020TD07).
Conflict of interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Publisher’s note
All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.
Supplementary material
The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fmars.2023.1166634/full#supplementary-material
References
Bochkarev N. A., Zuykova E. I., Abramov S. A., Podorozhnyuk E. V., Politov D. V. (2017). The sympatric whitefishes coregonus ussuriensis and c. chadary from the amur river basin: morphology, biology and genetic diversity. Fund Appl. Limnol. 189 (3), 193–207. doi: 10.1127/fal/2016/0801
Buchheister A., Wilberg M. J., Miller T. J., Latour R. J. (2015). Simulating bottom-up effects on predator productivity and consequences for the rebuilding timeline of a depleted population. Ecol. Model. 311, 48–62. doi: 10.1016/j.ecolmodel.2015.05.002
Froese R., Winker H., Coro G., Demirel N., Tsikliras A. C., Dimarchopoulou D., et al. (2018). A new approach for estimating stock status from length frequency data. ICES. J. Mar. Sci. 75, 2004–2015. doi: 10.1093/icesjms/fsy078
Gayanilo F. C., Sparre P., Pauly D. (2005). FAO-ICLARM stock assessment tools II (Rome: Worldfish Center).
Greve W. (1994). The 1989 German bight invasion of muggiaea atlantica. Ices. J. Mar. Sci. 51, 355–358. doi: 10.1006/jmsc.1994.1037
Guo Z. Q., Liu J. S., Lek S., Li Z. J., Zhu F. Y., Tang J. F., et al. (2016). Age, growth and population dynamics of two congeneric and invasive gobies, rhinogobius giurinus and r. cliffordpopei (Actinopterygii, gobiidae) in a plateau lake, southwestern China. Hydrobiologia 763, 69–79. doi: 10.1007/s10750-015-2361-7
Han J., Sun Z., Li Y., Yang Y. (2017). Combined effects of multiple large-scale hydraulic engineering on water stages in the middle Yangtze river. Geomorphology 298, 31–40. doi: 10.1016/j.geomorph.2017.09.034
Huo T. B., Song D., Liu W., Tang F. J., Wang J. L., Zhang L. L., et al. (2022). Status of early fish resources in the fujin section of the lower songhua river. J. Fishery Sci. China 29, 91–101.
Jiang X., Wang J., Pan B., Li D., Wang Y., Liu X. (2022). Assessment of heavy metal accumulation in freshwater fish of dongting lake, China: effects of feeding habits, habitat preferences and body size. J. Environ. Sci. 112, 355–365. doi: 10.1016/j.jes.2021.05.004
Li S. H., Han L., Wang Z. J., Wang L., Su G. Q., Di G. J. (2021). Study on swimming ability of crucian carp in songhua river. Hydro. Sci. Cold Zone Eng. 4, 33–37.
Li L., Ji F., Wang N. M., Jin H. Y., Zhang J. F., Ma B. (2018). Current status of fisheries resources in wutong river - the first order tributary of songhua river. Chin. J. Fish 31, 15–19.
Li L., Zhang Y., Zhang J., Ma B. (2020). Seasonal variation in diet of juvenile amur sturgeon acipenser schrenckii in the lower reaches of the songhua river, northeast China. J. Appl. Ichthyol. 36, 275–281. doi: 10.1111/jai.14041
Liu J., Cui Y., Liu J. (2000). Resting metabolism and heat increment of feeding in mandarin fish (Siniperca chuatsi) and Chinese snakehead (Channa argus). Comp. Biochem. Physiol. A Mol. Integr. Physiol. 127, 131–138. doi: 10.1016/s1095-6433(00)00246-4
Liu J. R., Dong H. W., Tang X. L., Sun X. R., Han X. H., Chen B. Q., et al. (2009). Genotoxicity of water from the songhua river, China, in 1994-1995 and 2002-2003: potential risks for human health. Environ. pollut. 157, 357–364. doi: 10.1016/j.envpol.2008.10.004
Lu X. X., Gu Y. G., Wang Z. H., Liang R. Z., Han Y. J., Li H. S. (2022). Risk on assessment of 15 REEs and mixtures by DGT in songhua river system sediments of china's largest old industrial base. Environ. Res. 212, 113368. doi: 10.1016/j.envres.2022.113368
Lu W. Q., Li P. L., Tang F. J., Yin Z. Q., Wang J. L., Abramov S. A. (2021). Population variation and resources rational utilization of hypophthalmichthysmolitrix in the trunk stream of the songhua river. Wetl. Sci. 19, 551–557.
Ma M., Liu S., Su M., Wang C., Ying Z., Huo M., et al. (2022). Spatial distribution and potential sources of microplastics in the songhua river flowing through urban centers in northeast China. Environ. pollut. 292, 118384. doi: 10.1016/j.envpol.2021.118384
Maitra S., Harikrishnan M., Shibu A. V., Sureshkumar S., Ranjeet K., Bijoy Nandan S. (2018). Studies on temporal variations of exploited fishery resources and their trophic levels in a tropical estuary. Reg. Stud. Mar. Sci. 22, 61–69. doi: 10.1016/j.rsma.2018.06.004
Mehanna S. F. (2007). Stock assessment and management of the Egyptian sole solea aegyptiaca chabanaud 1927 (Osteichthyes: soleidae), in the southeastern Mediterranean, Egypt. Turk. J. Zool. 31, 379–388.
Newman S. J. (2002). Growth, age estimation and preliminary estimates of longevity and mortality of the Moses perch, lutjanus russelli (Indian ocean form), from continental shelf waters off north-western Australia. Asian Fish Sci., 286–294. doi: 10.33997/j.afs.2002.15.3.009
Pauly D. (1980). On the interrelationships between natural mortality, growth parameters, and mean environmental temperature in 175 fish stocks. J. Conserv. Inter. Explor. Marit. 39, 175–192. doi: 10.1093/icesjms/39.2.175
Pauly D. (1981). The relationship between gill surface area and growth performance in fish: a generalization of von bertalanffy's theory of growth. Meeresforschung 4, 251–282.
Pauly D. (1982). “Studying single-species dynamics in a tropical multispecies context,” in Theory and Management of Tropical Fisheries ICLARM Conference Proceedings, Vol. 9. 33–70 (ICLARM).
Pauly D. (1983). Length-converted catch curves: a powerful tool for fisheries research in the tropics (Part I). Fishbyte 1, 9–13.
Pauly D. (1984). Length-converted catch curves: a powerful tool for fisheries research in the tropics (Part II) (Manila, Philippine: ICLARM Fishbyte), 17–19.
Pauly D. (1987). “A review of the ELEFAN system for analysis of length-frequency data in fish and aquatic invertebrates,” in Proceedings of ICLARM Conference on Length-Based Methods in Fisheries Research, Manila. (Manila, Philippines: ICLARM), 7–34.
Pauly D. (1990). Length-converted catch curves and the seasonal growth of fishes. Fishbyte 8, 33–38.
Pauly D., David N. (1981). ELEFAN I, a basic program for the objective extraction of growth parameters from length-frequency datal. Meeresforschung 4, 205–211.
Pauly D., Munro J. L. (1984). Once more on growth comparisons in fishes and inverte-brates (21: Fishbyte).
Pauly D., Soriano M. L. (1986). “Some practical extension of beverton and holts relative yield per-recruit model,” in The first Asian fisheries forum. Eds. Maclean J. L., Dizon L. B., Hosillo L. V. (Manila Philippines: Asian Fishers Society), 491–496.
Pauly D., Soriano-Bartz M., Moreau J., Jarre-Teichmann A. (1992). A new model accounting for seasonal cessation of growth in fishes. Mar. Freshw. Res. 43, 1151–1156. doi: 10.1071/MF9921151
Quinn I. I. T., Deriso R. B. (1999). Quantitative fish dynamics (New York: Oxford University Press).
Ricker W. E. (1975). Computation and interpretation of biological statistics of fish population (Canada: Bulletin of Fisheries Research Board).
Sharp G. D. (2001). Tuna oceanography–an applied science. Fish Physiol. 19, 345–389. doi: 10.1016/S1546-5098(01)19010-2
Thangaraj J. R., Muthukumarasamy S., Theivasigamani M., Retnamma J. (2022). Trophic ecology of four species of emperor fish (Lethrinus) in the gulf of mannar along the Indian southeast coast. Reg. Stud. Mar. Sci. 53, 102442. doi: 10.1016/j.rsma.2022.102442
Wang J. L., Li P. L., Tang F. J., Lu W. Q., Liu W. (2021). Screening of growth model for growth of silver carp hypophthalmichthys molitrix from main streams of songhua river. Chin. J. Fish 34, 35–39.
Wang J. L., Liu W., Li P. L., Lu W. Q., Tang F. J. (2020). Age and growth characteristics of silver carp (Hypophthalmichthys molitrix) in the main stream of songhua river. Chin. Agr. Sci. Bull. 36, 140–146.
Wang X., Wang W. X. (2019). The three 'B' of fish mercury in China: bioaccumulation, biodynamics and biotransformation. Environ. pollut. 250, 216–232. doi: 10.1016/j.envpol.2019.04.034
Ware D. M., Thomson R. E. (2005). Bottom-up ecosystem trophic dynamics determine fish production in the northeast pacific. Science 308, 1280–1284. doi: 10.1126/science.1109049
Wei C. F. (2018). Study on the health evaluation of the main stream of songhua river (Changchun, China: Northeast Institute of Geography and Agroecology, Chinese Academy of Sciences), 165.
Xie Y. H. (2007). Freshwater fishes of northeast China (Shenyang: Liaoning Science and Technology Publishing House).
Yang Z. F., Hu P., Wang J. H., Zhao Y., Zhang W. H. (2019). Ecological flow process acknowledging different spawning patterns in the songhua river. Ecol. Eng. 132, 56–64. doi: 10.1016/j.ecoleng.2018.12.034
Yang F. Y., Yan B. X., Wang Q., Luan Z. Q., Tong S. Z. (2015). Assessment of fish stocks in the lower reaches of the songhua river. Wetland Sci. 13, 87–97.
Yin Z. Q., Lu W. Q., Chen Y., Liu Y. H., Zhou S. L., Meng W. D., et al. (2016). Growth characteristics and resource evaluation of sebastes schlegelii in zhangzidao artificial reef area. Anim. Husbandry Feed Sci. 8, 186–188.
Yu X. F., Ding S. S., Zou Y. C., Xue Z. S., Lyu X. G., Wang G. P. (2018). Review of rapid transformation of floodplain wetlands in northeast China: roles of human development and global environmental change. Chin. Geogr. Sci. 28, 654–664. doi: 10.1007/s11769-018-0957-3
Zhang J. M. (1991). Handbook of fisheries natural resource surveys in inland waters (Beijing: Agriculture Press).
Zhang J. M. (1995). Fishes of heilongjiang province (Harin: Heilongjiang Science and Technology Press).
Keywords: prey fish, ecosystem, FISAT II, population dynamics, fishery management, Songhua River
Citation: Lu W, Li P, Ma B, Huo T, Yin Z, Tang F and Wang J (2023) Assessment of fishery management parameters for major prey fish species in the lower reaches of the Songhua River. Front. Mar. Sci. 10:1166634. doi: 10.3389/fmars.2023.1166634
Received: 15 February 2023; Accepted: 02 June 2023;
Published: 16 June 2023.
Edited by:
Yang Jin, Carnegie Institution for Science, United StatesReviewed by:
Carlos Freitas, Federal University of Amazonas, BrazilHadayet Ullah, WorldFish, Malaysia
Copyright © 2023 Lu, Li, Ma, Huo, Yin, Tang and Wang. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Jilong Wang, wangjilong@hrfri.ac.cn