Performance of indicators derived from abundance estimates for detecting the impact of fishing on a fish community

2003 ◽  
Vol 60 (1) ◽  
pp. 67-85 ◽  
Author(s):  
Verena M Trenkel ◽  
Marie-Joëlle Rochet

Population and community indicators for the impact of fishing are often estimated using abundance estimates instead of raw sampling observations. Methods are presented for testing null hypotheses of nonsignificant impacts and, where possible, for calculating the statistical power. The indicators considered concern populations (intrinsic growth rate, total mortality, exploitation rate, and a new indicator, the change in fishing mortality required to reverse population growth) and communities (k- and partial-dominance curves, a biodiversity index, size spectrum, and proportions of various population groups). The performance of these indicators is compared for the Celtic Sea groundfish community based on achieved precision, statistical power, and availability and estimation method of reference points. Among population indicators, mean length of catch was most precisely estimated and the corresponding hypothesis tests had consistently large powers. Total mortality performed reasonably well. In contrast, both the intrinsic population growth rate and the exploitation rate gave unreliable results. All tested community indicators performed similarly well. Indicators for which the direction of change caused by fishing is predictable, such as the proportion of noncommercial species or piscivores in the community, are promising indicators at the community level.

2003 ◽  
Vol 60 (1) ◽  
pp. 86-99 ◽  
Author(s):  
Marie-Joëlle Rochet ◽  
Verena M Trenkel

Population and community descriptors that might be used as indicators of the impact of fishing are reviewed. The criteria used for the evaluation of these indicators are meaning, expected effect of fishing, exclusiveness to fishing effects, and measurability. Population indicators such as total mortality rate, exploitation rate, or average length are the most operational indicators because their meaning is clear and the expected effect of fishing on them is well understood so that reference points can be set. On the other hand, indicators based on the composition of species assemblages such as diversity indices and ordination of species abundances are difficult to interpret, and the effect of fishing on them is not easily predicted. Robust indicators describing the community functions of interest (production and transfer of biomass to large fish), such as size spectra descriptors or the proportion of piscivorous fish in the community, are more promising but are not yet well developed. New candidate indicators are proposed: the change in fishing mortality required to reverse population growth rate, the proportion of noncommercial species in the community, and the average length and weight in the community.


2019 ◽  
Vol 36 (4) ◽  
pp. 319-324
Author(s):  
İsmet Balık

The aim of this study is to estimate population parameters of pontic shad, Alosa immaculata Bennett, 1835 in the Fatsa coast of the south-eastern Black Sea. A total of 314 pontic shad specimens were collected from study area using artisanal fishing gears from March 2013 to February 2014. In the study, parameters of the von Bertalanffy growth equation were found as L∞=43.05 cm; k=0.430 per year and t0=-0.451 year. The growth performance index (Φ') was estimated as 2.90. The total mortality (Z), natural mortality (M), fishing mortality rates (F) were calculated as 1.33 year-1, 0.75 year-1 and 0.58 year-1, respectively. The annual instantaneous fishing mortality rate was greater than both the target (Fopt=0.375 year-1) and limit (Flimit=0.50 year-1) biological reference points. Similarly, the present level of exploitation rate (E=0.43) was higher than the exploitation ratio for maximum yield per recruit (Emax=0.375) suggesting that overexploitation occurred. These results showed that this species has been over-exploited in the Fatsa coast of the south-eastern Black Sea. Measures should be taken to reduce the current exploitation rate for sustainable fishing of pontic shad in the Fatsa coast of the south-eastern Black Sea.


2018 ◽  
Vol 14 (1) ◽  
pp. 16
Author(s):  
Dini Sofarini ◽  
Mohammad Mahmudi ◽  
Asus Maizar S. Hertika ◽  
Endang Yuli Herawati

The province of South Kalimantan has the largest peat swamp that is named Danau Panggang Swamp with an area of 5,390.7 Ha. This swamp has ecological, economic and potential functions of a large fishery resource. The purposes of this study are to evaluate the exploitation rate of Snake Head Fish (Channa striata) in Danau Panggang Swamp, by population dynamic analysis using FISAT program of Von Bertalanffy method.  The results showed that the growth pattern of Snake Head Fish (Channa striata) has the tendency to grow negative allometric with 63.4 cm of long infifer (L¥), growth rate (k) 0.15 per year, theoretical age at the time of the fish is equal to 0 (t0) is -1.48257 years. While the natural mortality rate (M) was 0.43, the mortality rate due to catch (F) of 0.69/year and the total mortality rate  (Z) of 1.12/year, and the rate of exploitation value E = 0.62.  These results indicated that the exploitation rate of Head Snake Fish (Channa striata) in Danau Panggang swamp has a tendency to overfishing.


PeerJ ◽  
2021 ◽  
Vol 9 ◽  
pp. e10708
Author(s):  
Douglas C. Heard ◽  
Kathryn L. Zimmerman

Most woodland caribou (Rangifer tarandus caribou) populations are declining primarily because of unsustainable predation resulting from habitat-mediated apparent competition. Wolf (Canis lupus) reduction is an effective recovery option because it addresses the direct effect of predation. We considered the possibility that the indirect effects of predation might also affect caribou population dynamics by adversely affecting summer foraging behaviour. If spring and/or summer nutrition was inadequate, then supplemental feeding in fall might compensate for that limitation and contribute to population growth. Improved nutrition and therefore body condition going into winter could increase adult survival and lead to improved reproductive success the next spring. To test that hypothesis, we fed high-quality food pellets to free-ranging caribou in the Kennedy Siding caribou herd each fall for six years, starting in 2014, to see if population growth rate increased. Beginning in winter 2015–16, the Province of British Columbia began a concurrent annual program to promote caribou population increase by attempting to remove most wolves within the Kennedy Siding and the adjacent caribou herds’ ranges. To evaluate the impact of feeding, we compared lambdas before and after feeding began, and to the population trend in the adjacent Quintette herd over the subsequent four years. Supplemental feeding appeared to have an incremental effect on population growth. Population growth of the Kennedy Siding herd was higher in the year after feeding began (λ = 1.06) compared to previous years (λ = 0.91) and to the untreated Quintette herd (λ = 0.95). Average annual growth rate of the Kennedy Siding herd over the subsequent four years, where both feeding and wolf reduction occurred concurrently, was higher than in the Quintette herd where the only management action in those years was wolf reduction (λ = 1.16 vs. λ = 1.08). The higher growth rate of the Kennedy Siding herd was due to higher female survival (96.2%/yr vs. 88.9%/yr). Many caribou were in relatively poor condition in the fall. Consumption of supplemental food probably improved their nutritional status which ultimately led to population growth. Further feeding experiments on other caribou herds using an adaptive management approach would verify the effect of feeding as a population recovery tool. Our results support the recommendation that multiple management actions should be implemented to improve recovery prospects for caribou.


2019 ◽  
Vol 20 (4) ◽  
pp. 1051-1068 ◽  
Author(s):  
Sushant Kumar ◽  
Vishlavath Giridhar ◽  
Pradip Sadarangani

The study investigates the impact of culture on environmental performance across 78 countries. The article explores the possible relationship with two datasets of international indices: (a) the six dimensional index of national culture proposed by Hofstede and (b) the environmental performance index (EPI) published by Yale Center for Environmental Law and Policy. It is widely established that population and economic development of a country play significant role in the improvement of environmental performance. In our study, we examine the impact of population growth rate and per-capita gross domestic product (GDP) on environmental performance using structure equation modelling. The results show that environmental performance is significantly influenced by the culture of the country. Per-capita GDP and population growth rate have a positive and negative relationships on the environmental performance. By measuring the cultural dimensions and their impact on global environmental performance, countries could identify the favouring cultural dimensions and design appropriate strategy to optimize the environmental performance. The article proposes the practical implication of results and strategies to improve environmental performance. The study is among the first in studying the cultural dynamics on environment and identify its favourable and adverse relationships for an optimum strategy.


2019 ◽  
pp. 1-28
Author(s):  
Alberto Bucci ◽  
Lorenzo Carbonari ◽  
Giovanni Trovato

We provide aggregate macroeconomic evidence on how, in the long run, a diverse degree of complexity in production may affect not only the rate of economic growth, but also the correlation between the latter, population growth and the monopolistic (intermediate) markups. For a sample of Organisation for Economic Co-operation and Development (OECD) countries, we find that the impact of population change on economic growth is slightly positive. According to our theoretical model, this implies that the losses due to more complexity in production are lower than the corresponding specialization gains. Using a finite mixture model, we also classify the countries in the sample and verify for each cluster the impact that the population growth rate and the intermediate sector’s markups exert on the 5-year average real gross domestic product (GDP) growth rate.


2010 ◽  
Vol 37 (7) ◽  
pp. 588 ◽  
Author(s):  
Brian Chambers ◽  
Roberta Bencini

Context Although road mortality has the potential to affect the fate of populations, it is often confounded with other forms of environmental change. Therefore determining its impact separately from other factors is difficult because it requires an understanding of how road mortalities affect age- and sex-specific survival rates. Aims We determined the impact of high numbers of road-kills and habitat modification on the growth and survival of the population of tammar wallabies (Macropus eugenii) on Garden Island, off the coast of Western Australia. The increased supply of food from large areas of fertilised and irrigated lawns on a naval base was expected to increase the population growth rate (λ) and the road-kills were expected to offset the population response. Methods We conducted a mark-and-recapture study over three years to estimate rates of survival, reproduction and population growth rates in areas of the island that were either heavily affected by the presence of a naval base that included a network of roads and buildings, close enough to the naval base that animals could be affected by the disturbance there, and completely unaffected and lacking major roads or buildings. All road-kills were collected to estimate the impact of road mortality on the survival and growth rates of the population. Key results The growth rate, λ, for the population on the naval base was 1.02 ± 0.083 (s.e.) per year, which was much higher than in an area of adjacent bushland at 0.92 ± 0.065 per year and in undisturbed bushland at 0.93 ± 0.100 per year. When the impact of road mortality was removed, λ increased to 1.15 ± 0.101 per year on the naval base and 0.96 ± 0.076 per year in the bushland adjacent to the naval base. On the naval base road mortality reduced survival rates of one-year-old and adult animals by 0.14 ± 0.087 and 0.12 ± 0.012 per year (mean ± s.e.). Conclusions Road mortality counteracted the increase in the size of the tammar population caused by the habitat modification on the naval base. The impact of road mortality on the adjacent bushland population may result in its long-term decline, as the population may not be able to recover from the reduction in survival rates. Implications Road mortality has the potential to threaten susceptible populations but its impact should be quantified so that mitigation measures can be implemented where they will achieve the greatest benefits.


2017 ◽  
Vol 4 (3) ◽  
pp. 237-248
Author(s):  
Samuel KK Amponsah ◽  
Patrick K Ofori Danson ◽  
Francis KE Nunoo ◽  
Godfred A Ameyaw

Following the declining stocks of Sardinella aurita within the coastal waters of Ghana, this study aimed at examining some population parameters of Sardinella aurita as a guide for managing this important stock sustainably. Length-frequency data of 717 samples were obtained from June, 2014 to January 2015 and measured for total length with the resultant data analyzed using FiSAT II. The asymptotic length (L∞) and growth rate (K) were 21.53 cm SL and 0.25yr-1 respectively. The theoretical age at birth (t0), longevity (tmax) and growth performance index (ϕ) were -0.74yr-1, 12 years and 1.849 respectively. Total mortality rate (Z), natural mortality rate (M) and fishing mortality rate (F) were 3.17, 0.76 and 2.41yr-1 respectively. The ages at first recruitment and first capture signaled future collapse of the stock, in the absence of proper management interventions. VPA outcome showed that mid- lengths of 11 cm and 12 cm SL experienced the highest harvesting rate with MSY estimated at 7733 tons. The recruitment pattern was continuous with two major recruitment pulses. Exploitation rate (Ecurr=0.76) was higher than the maximum exploitation rate (Emax=0.56), indicating unsustainable exploitation. Further, the fishing regime fell within the overfished stage based on the Quadrant Rule. For sustainable exploitation of this commercial fish species, implementation of relevant biological reference points through reduction in fishing efforts, creation of marine protected areas and mesh size regulation are urgently advocated.Res. Agric. Livest. Fish.4(3): 237-248, December 2017


2017 ◽  
Vol 9 (2) ◽  
pp. 113
Author(s):  
Thomas Hidayat ◽  
Tegoeh Noegroho ◽  
Karsono Wagiyo

Ikan cakalang (Katsuwonus pelamis Linnaeus, 1758) merupakan salah satu sumberdaya ikan pelagis besar yang mempunyai nilai ekonomis penting. Informasi mengenai struktur ukuran dan beberapa parameter populasinya masih sangat terbatas khususnya di perairan Indonesia timur. Penelitian ini dilakukan di Morotai, Biak dan Jayapura dari Januari sampai Desember 2013. Tujuan penelitian ini adalah untuk menganalisis ukuran ikan yang tertangkap dan menganalisis parameter populasi meliputi laju pertumbuhan, mortalitas dan tingkat eksploitasi. Estimasi parameter pertumbuhan, mortalitas dan laju eksploitasi dihitung menggunakan program FiSAT (FAO-ICLARM Stock Assessement Tools). Ukuran ikan cakalang hasil tangkapan pancing tonda dan pancing ulur berkisar antara 15 – 94 cmFL (Fork Length), dengan modus antara 40-45 cmFL. Ukuran pertama kali tertangkap sebesar 40,1 cmFL dan kebanyakan adalah ukuran ikan yang sedang memijah. Hasil analisis menggunakan FiSAT II diperoleh laju pertumbuhan (K) sebesar 0,41/tahun, panjang asimptotik (L) 101,85 cmFL. Laju kematian alami (M) 0,6 / tahun, laju kematian karena penangkapan (F) 0,62 /tahun dan laju mortalitas total (Z) 1,22 /tahun. Tingkat eksploitasi ikan cakalang hampir fully exploited (E= 0,46). Disarankan tidak perlu ada penambahan upaya penangkapan atau status quo untuk menjaga agar sumberdaya ikan cakalang tetap terjaga kelestariannya. Skipjack tuna (Katsuwonus pelamis Linnaeus, 1758) is one of the large pelagic fish resources which have high economic value. Information on the size structure and population parameters is still limited especially in the waters of eastern Indonesia. The Research was conducted from January to December 2013 at Morotai, Biak and Jayapura. The aim of this study was to analyze the size of the fish caught and some of population parameters such as the growth rate, mortality rates, and exploitation rate. Estimated of growth parameters, mortality and exploitation rate using the program FiSAT (FAO-ICLARM Stock Assessement Tools). The size of skipjack tuna caught by troll line and handline in between 15-94 cmFL, with a mode of 40-45 cmFL. The Length at first capture was 40.1 cmFL, most of them had condition of spawning. By using program FiSAT II analysis resulted that growth rate (K) of skipjack tuna was 0.41/year, with length asimptotik (L) reaches 101.85 cmFL. The natural mortality rate (M) was 0.6 / year. The fishing mortality rate (F) was 0.62 / year and total mortality rate (Z) was 1.22 / year. The exploitation rate of skipjack tuna was nearly fully exploited (E = 0.46). It was recommended the exploitation rate of this fish should be no additional effort (status quo) to keep sustainability of the skipjack tuna resource.


2020 ◽  
Vol 15 (9) ◽  
pp. 53
Author(s):  
Phan Văn Trung ◽  
Nguyễn Thám

 The Be river basin is located in the area with a rapid urbanization rate and a large immigrants proportion annually. Therefore, the population growth rate for the period from 2000 to 2015 in the river basin is up 3,53% which is 3,27 times as high as the population growth rate of Vietnam. These are the major causes leading to the fluctuation in vegetation cover of the Be river basin during over time. This research used methodologies including data collection, statistical analysis, mapping method and geographic information system to evaluate the impact of human factors to the vegetation cover fluctuation of the Be river basin in the period from 2000 to 2015. Based on the results of change map in the vegetation cover, a research group set up fluctuating matrix, analyze to clarify the vegetation coverfluctuation situation due to human’s impacts in the Be river basin in the period from 2000 to 2015. 


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