Indian Journal of Animal Research

  • Chief EditorK.M.L. Pathak

  • Print ISSN 0367-6722

  • Online ISSN 0976-0555

  • NAAS Rating 6.40

  • SJR 0.263

  • Impact Factor 0.4 (2024)

Frequency :
Monthly (January, February, March, April, May, June, July, August, September, October, November and December)
Indexing Services :
Science Citation Index Expanded, BIOSIS Preview, ISI Citation Index, Biological Abstracts, Scopus, AGRICOLA, Google Scholar, CrossRef, CAB Abstracting Journals, Chemical Abstracts, Indian Science Abstracts, EBSCO Indexing Services, Index Copernicus
Indian Journal of Animal Research, volume 55 issue 12 (december 2021) : 1515-1520

Population Viability Analysis of Yangtze Finless Porpoise in the Yangtze Main Steam Suggesting that a Total Ban on Productive Fishing could be Decisive

Wu Bin1, Xu Jingen2, Wang Jianmin2, Cao Lie2, Wang Weiping3, Zhang Song2
1Jiangsu Key Laboratory for Biodiversity and Biotechnology, College of Life Sciences, Nanjing Normal University, 210 023 Nanjing, China.
2Fisheries Research Institute of Jiujiang city, 332 000, Jiujiang, China.
3Aquatic Biology Protection and Rescue Center of Jiangxi Province, 330 000 Nanchang, China.
Cite article:- Bin Wu, Jingen Xu, Jianmin Wang, Lie Cao, Weiping Wang, Song Zhang (2021). Population Viability Analysis of Yangtze Finless Porpoise in the Yangtze Main Steam Suggesting that a Total Ban on Productive Fishing could be Decisive . Indian Journal of Animal Research. 55(12): 1515-1520. doi: 10.18805/IJAR.B-1353.
Background: China is paying more attention to ecological systems within the Yangtze River has provided great opportunities to the conservation of the Yangtze finless porpoise (YFP). The rapid population decline of YFP in the main steam appears to have slowed, but the infrequent movement of porpoises represents a considerable threat to the long-term viability of this species in this region. We studied the population viability of YFP in the Yangtze main steam, based on published ecological and genetic information.

Methods: Vortex model was used to analyze the population viability of the YFP. The simulations were started from the year 2017 when the initial population size was 445 animals in baseline scenario. We examined the population viability for the species under demographic fluctuations and conservation scenarios.

Result: Baseline model showed the probability of extinction was 0.245; deterministic growth rate was -0.023; stochastic growth rate was -0.036. Sensitivity analysis showed differences in population trends between the baseline and each alternative scenario and the most sensitive parameters were the percentage of females breeding and mortality rates. Under different conservation scenarios, the population of the YFP in the main stream will increase by 11.0%-181.2% in 100 years.
In recent years, the species extinction rate has accelerated worldwide and is a thousand times higher than through natural processes alone (IUCN, 2010). Population dynamic models have been successfully applied in aquatic animal protection and resource assessment (Zhang and Wang 1999; Hacer, 2018; Wu et al., 2018, 2020a; Huang et al., 2020). Population viability analysis (PVA) is a tool for endangered species management and conservation due to the focus on species limitation factors (Brook et al., 2000).
       
The use of PVA results in conservation decision making has been recommended partly because they are thought to be objective and repeatable (Doak et al., 2015). PVA has been a core methodology, a lot has been learned about the factors determining the dynamics of wildlife populations and about techniques for assessing viability (Lacy, 2018). Furthermore, many PVA studies may not have sufficient data to perform model validation or test predictive accuracy. Well-conducted PVA studies guided by specific questions have intrinsic values, even if they lack long-term data or do not test for predictive accuracy (Vratika and Madan 2020).
       
The Yangtze finless porpoise (YFP, Neophocaena asiaeorientalis) is a small, freshwater toothed porpoises that occurs only in the middle and lower reaches of the Yangtze River (from Yichang to Shanghai) and its adjoining lakes (Poyang and Dongting lake) (Gao et al., 1995) it is genetically isolated from other porpoise populations and reveal the genomic signatures of adaptation to the freshwater environment of this incipient species (Zhou et al., 2018). As the baiji (Lipotes vexillifer) is probably extinct (Turvey et al., 2007, Wu et al., 2020a), the YFP is the only cetacean to inhabit the Yangtze River catchment area. The immigration and emigration of the YFP between the main stream and the lakes (Poyang Lake and Dongting Lake) has basically disappeared (Zhao et al., 2008; Huang et al., 2020).
       
This is particularly true for species occurring in multiple populations, each of which may require a separate PVA (Helen et al., 2019). In this study Vortex 10.3.7.0) was used to analyze the population viability of YFP in the Yangtze main steam the best way to improve population vulnerability (Lacy et al., 2017). The program is chosen because it is powerful, easily available, tried and tested and continuously updated.
In Yangtze River main stream waters, the mean annual growth rate from 2012 to 2017 was l=0.975 the estimated abundance of YFP were 445 animals (CV=17.19%, 95% CI: 295-595), of which 106 were in the upper region, 103 were in the middle region 236 were in the lower region (Huang et al., 2020). The population of YFP in Yangtze River is disjunct and isolated (Zhang, 2011; Huang et al., 2020); Hence we assumed that immigration and emigration were unlikely to occur between the Yangtze River and the lakes that connect it (Poyang Lake and Dongting lake). The simulations were started from the year 2017, due to lack of available data for the subsequent years when the initial population size was 445 animals in baseline scenario.
 
Mating system and mortality rate
 
YFP is polygynous specie that reproduce between 4 year (age of first offspring females) and up to 18 years of age (maximum age of female reproduction), the babies have a birth ratio of 1: 1 and 1 litter per litter (Hao et al., 2006, Chen et al., 2016, Li 2017). The YFP breeding cycle is generally 2 years (Zhang et al., 1992). However, some YFP have overlapping lactation and pregnancy periods (Shirakihara et al., 1993), so the annual reproductive rate of the YFP is 50%, but it can reach 70% (Zhang et al., 1992, Yang et al., 1998).
       
The mortality rate of the YFP is 25% in the first year of life, 20% in the second year of life and 10% there after (Yang et al., 1998, Zhang and Wang, 1999, Li, 2017).
 
Disasters
 
VORTEX model recommendation sets natural disasters as the probability of a severe die-off for a particular population is approximately 14% per generation they define a catastrophe as any 1-year decrease in population size of 50% or greater (Reed et al., 2003). VORTEX model calculation of the YFP generation was 8-9 years, thus natural disaster scenario was set as the probability 1.75%, which simulated the population dynamics at 50% survival and reproduction rate, respectively. The number of registered dead YFP fluctuates periodically from peak to valley, possibly with a cycle of 6 years (Wu et al., 2020b). Therefore, human catastrophe scenario was set as the probability 16.7%, which simulated the population dynamics at 99% survival and reproduction rates, respectively.
 
Environmental capacity and in breeding
 
The environmental capacity of YFP is 5,000 animals in the Yangtze River (Zhang et al., 1999). Therefore, we estimate that the environmental capacity of YFP in the main stream of the Yangtze River was 3000 animals. And the near-bank area (km2) of the upper region, middle region lower region Yangtze main steam are 401, 256 707, so the environmental capacity was 1000, 800 1200 animals, respectively.
       
Ralls et al., (1988) studied the lethal equivalence coefficient of 40 mammalian populations and concluded that each diploid had 3.14 lethal gene equivalents. So, set 3.14 as the lethality equivalence coefficient of the YFP.
       
We defined that extinction occurs only when one sex remained in the population. Each simulation was performed with 10000 iterations in 100 years, the calculation times were 10 times of the usual, so it was more stable and reliable.
Population dynamics in baseline model
 
The probability of extinction was 0.245 for metapopulation, 0.566 for upper region population, 0.450 for middle region population 0.447 for lower region population, but there was almost no extinction probability within 30 years. The genetic diversity was on a continuous downward trend and the simulations presented here predict severe declines YFP population in the Yangtze main steam by 94.0% in 100 years, as shown in Fig 1.
 

Fig 1: Population viability dynamics of YFP in the Yangtze main steam in baseline model (a, Population size; b, Genetic diversity; c, Survival probability; d, Extinction time frequency).


       
In Europe, vulture population declines began in the mid-19th century leading to local extinctions of some species (Ogada et al., 2012). In the early 21st century, vulture populations showed a more stable and slightly increasing trend due to changes in European legislation (Margalida et al., 2010) and intensive management and conservation (Margalida et al., 2010; Donázar et al., 2009). The newly revised List of Key State Protected Wild Animals in 2021 confirmes that the YFP is officially promoted to the first class of protected wild animals in China. The major threats to the YFP include overfishing and illegal fishing, pollution, vessel traffic and construction over the last four decades, to a point where this species is classified as Critically Endangered on the IUCN Red List of Threatened Species (Wang et al., 2005). Therefore, we believe that a total ban on productive fishing, intensive management and conservation would have a decisive positive effect on the protection of the YFP in the main stream.
 
Sensitivity analysis and conservation scenarios
 
Our analysis also examined the sensitivity of dispersal, the maximum reproductive age, breeding rate, mortality rate, initial population size, carrying capacity, Model 2-14 were formed respectively. Models 2 and 4 predict a 92.4-92.2% population decline, Models 5 and 6 predict a 99.2-87.8% population decline, Model 7 predict a 100% population decline, Model 8 predict a 218.3% population rise, Models 9 and 10 predict a 99.2-69.4% population decline, Models 11 and 12 predict a 97.2-90.7% population decline, Models 13 and 14 predict a 94.1-94.0% population decline, in 100 years. Compare the deterministic growth rate (Det-r) and stochastic annual population growth rate (Stoch-r), it was not difficult to find that breeding rate mortality rate that would be more sensitive to maintain population stability.
           
Population projections to 2025 and 2050 predicted continued population declines of Hector’s and Maui dolphins under the current protection measures. But all risk analyses to date showed that without fisheries mortality, were predicted to recover, potentially up to half of their original population size by 2050 (Slooten and Dawson 2010, Slooten and Davies 2011). If there is enough food, the breeding interval will be relatively short (He et al., 2020). A total ban on productive fishing reinforces natural food availability and increases pre-adult survival, thus constitutes an important management practice for the conservation of YFP in the main stream. In addition, we speculate that the immigration and emigration of YFP in different sections of the main stream will gradually recover. Therefore, we construct two protection scenarios, mitigation conservation scenario (Model 15) and comprehensive improved conservation scenario (Model 16). Models 15 and 16 predict a 11.0%-181.2% population rise in 100 years, but even under Model 16, it would take about 60 years for the population to double, results were shown in Fig 2 and 3. Models 1-16 and their output are summarized in Table 1. Our models suggested that juvenile mortality, habitat restoration, connectivity dispersal were far more pertinent and should be among the highest priorities for future conservation management and planning.
 

Table 1: The deterministic growth rate (Det-r), stochastic growth rate (Stoch-r) and population size change (%) in 100 years under different scenarios.


 

Fig 2: Population viability dynamics of YFP in the Yangtze main steam in mitigation conservation scenario (a, Population size; b, Genetic diversity; c, Survival probability; d, Extinction time frequency).


 

Fig 3: Population viability dynamics of YFP in the Yangtze main steam in comprehensive improved conservation scenario (a, Population size; b, Genetic diversity; c, Survival probability; d, Extinction time frequency).

We provided a YFP baseline population viability model using multi-data source. Baseline scenario showed that this population was in a relatively vulnerability state in 100 years. This work highlights the importance of understanding how demographic fluctuations and conservation scenarios parameters affect long-term persistence of the threatened YFP and may provide knowledge fundamental to the understanding of other similar species. We have highlighted parameters critical for YFP persistence and discussed how variation in conservation scenarios may alter YFP population outcomes. From our models, we can infer that the long-term viability of YFP heavily relies on habitat restoration and diffusion connectivity.

  1. Brook, B.W., O’grady, J.J. and Chapman, A.P., et al. (2000). Predictive accuracy of population viability analysis in conservation biology. Nature. 404(6776): 385-387.

  2. Chen, M.M., Zheng, Y. and Hao, Y.J., et al. (2016). Parentage Based Group Composition and Dispersal Pattern Studies of the Yangtze Finless Porpoise Population in Poyang Lake. International Journal of Molecular Sciences. 8: 1268.

  3. Donázar, J.A., Margalida, A. and Carrete, M., et al. (2009). Too sanitary for vultures. Science. 326: 664.

  4. Doak, D.F., Himes B.G.K. and Bakker V.J., et al. (2015). Recommendations for improving recovery criteria under the US Endangered Species Act. BioScience. 65:189-199.

  5. Gao, A. and Zhou, K. (1995). Geographical variation of external measurements and three subspecies of Neophocaena phocaenoides in Chinese waters. Acta Theriol. Sin. 15: 81-92.

  6. Hao, Y.J, Wang, D., Zhang, X.f. (2006). Review on breeding biology of Yangtze finless porpoise (Neophocaena phocaenoides asiaeorientalis), Acta Theriologica Sinica of China. 26(2): 191-200.

  7. Hacer Y. (2018). Estimating some population parameters and stock assesment of spiny butterfly ray, Gymnura altavela (Linnaeus, 1758) the Levant Basin coast (Northeastern Mediterranean). Indian J. Anim. Res. 52(12): 1790-1796.

  8. Huang, J., Mei, Z.G. Chen, M. et al. (2020). Population survey showing hope for population recovery of the critically endangered Yangtze finless. Biological Conservation. 241: 108315.

  9. Helen, M.N. Douglas, R.L. and Daniel, C.D. et al. (2020). Application of multiple-population viability analysis to evaluate species recovery alternatives. Conservation Biology. 34(2): 482-493.

  10. He, C.H., Du, J.J. and Zhu, D. et al. (2020). Population viability analysis of small population: a case study for Asian elephant in China. Integrative Zoology. 15: 350-362.

  11. IUCN. (2010). Biodiversity, It’s Now or Never. Available online: https://www.iucn.org/content/biodiversity-its-now-or-never.

  12. Lacy, R.C. and Pollak, J.P. (2017). Vortex: A Stochastic Simulation of the Extinction Process. Version 10.2.14. Chicago Zoological Society. Brookfield, Illinois, USA.

  13. Lacy, R.C. (2018). Lessons from 30 years of population viability analysis of wildlife populations. Zoo Biology. 1-11. https://doi.org/10.1002/zoo.21468.

  14. Li YT. (2017). Study on the habitat selection, environmental capacity population viability of the yangtze finless porpoises in Tian-e-zhou semi-natural ex situ reserve. Wuhan: Institute of Hydrobiology, the Chinese Academy of Sciences.

  15. Margalida, A., Donázar, J.A. and Carrete, M. et al. (2010). Sanitary versus environmental policies: Fitting together two pieces of the puzzle of European vulture conservation. J. Appl. Ecol. 47: 931-935.

  16. Ogada, D.L., Keesing, F. and Virani, M. (2012). Dropping dead: Causes and consequences of vulture population declines worldwide. Ann. N.Y. Acad. Sci. 1249: 57-71.

  17. Ralls, K, Ballou, J.D. and Templeton, A. (1988). Estimates of Lethal Equivalents and the Cost of Inbreeding in Mammals. Conservation Biology. 2: 185-193. 

  18. Reed, DH., O’Grady, J.J. and Ballou, J.D. et al. (2003). The frequency and severity of catastrophic die-offs in vertebrates. Animal Conservation. 6: 109-114.

  19. Shirakihara, M., Takemura, A. and Shirakhara, K. (1993). Age, growth reproduction of the finless porpoise. Nephocaena phocaenoides, in the coastal waters of western Kyuhu, Japan. Marine Mammal Science. 9(4): 392-406.

  20. Slooten, E. and S.M. Dawson. (2010). Assessing the effectiveness of conservation management decisions: Likely effects of new protection measures for Hector’s dolphin. Aquatic Conservation: Marine and Freshwater Ecosystems 20: 334-347.

  21. Slooten, E. and Davies. N. (2011). Hector’s dolphin risk assessments: Old and new analyses show consistent results. Journal of the Royal Society of New Zealand. 42:49-60.

  22. Turvey, S.T., Pitman, R.L. and Taylor, B.L. et al. (2007). First human-caused extinction of a cetacean species? Biol. Lett. 3: 537-540. 

  23. Vratika, C. and Madan K.O. (2020). A critical appraisal of population viability analysis. Conservation Biology. 34(1): 26-40.

  24. Wang, D., Hao, Y. and Wang, K., et al. (2005). Aquatic Resource Conservation. The first Yangtze finless porpoise successfully born in captivity. Environ. Sci. Pollut. Res. 12: 247-250.

  25. Wang, D., Turvey, S.T. and Zhao, X. et al., (2013). Neophocaena Asiaeorientalis ssp. asiaeorientalis. IUCN 2013. IUCN Red List of Threatened Species http://www.iucnredlist. org, Version 2013.1. Downloaded on 16 July 2013.

  26. Wu, B., Wang H.H. and Fu H.Y. et al. (2018). Estimating some population parameters and stock assessment of Dark Sleeper Odontobutis potamophila in the Gaosha River, Wuyuan County, Jiangxi Province. Indian J. Anim.Res. 52(5): 664-668.

  27. Wu, B., Wang, W.P. and Wang, H.H. et al. (2020a). A retrospective Analysis on the Population Viability of the Yangtze River Dolphin or Baiji (Lipotes vexillifer). Indian Journal of Animal Research. DOI: 10.18805/ijar.B-1238.

  28. Wu, B., Wang, W.P. and Wang, Q.P. et al., (2020b). Analysis of the number of dead Yangtze Finless porpoise based on grey prediction. (in Chinese) Bulletin of Biology. 55(9): 19-20. 

  29. Yang, G, Zhou, K.Y. Gao, A.L. et al. (1998). Study on life table and population dynamics of finless porpoises. (in Chinese) Acta zoologica sinica. 18(1): 1-7.

  30. Zhang, X.F. (1992). study on age identification, growth and reproduction of finless porpoises. Chinese Acta hydrobiologica sinica. 16(4): 289-297.

  31. Zhang, X.F. and Wang, K.X. (1999). Viability analysis of finless porpoise populations in the Yangtze river. Chinese Acta Ecologica Sinica. 19(4): 529-533.

  32. Zhao, X., Barlow, J. and Taylor, B.L. et al. (2008). Abundance and conservation status of the Yangtze finless porpoise in the Yangtze River. China. Biol. Conserv. 141: 3006-3018.

  33. Zhang, X.Q. (2011). Population ecology of Yangtze finless porpoise in Dongting Lake and adjacent waters. Wuhan: Institute of Hydrobiology, the Chinese Academy of Sciences.

  34. Zhou, X.M., Guang, X.M. and Sun, D. et al. (2018). Population genomics of finless porpoises reveal an incipient cetacean species adapted to freshwater [J]. Nature Communications. 9: 1276.

Editorial Board

View all (0)