Journal of Threatened Taxa |
www.threatenedtaxa.org | 26 June 2020 | 12(9): 16173–16176
ISSN 0974-7907 (Online) | ISSN 0974-7893
(Print)
doi: https://doi.org/10.11609/jott.5961.12.9.16173-16176
#5961 | Received 07 April 2020 | Final
received 05 May 2020 | Finally accepted 06 June 2020
The niche of shrimp stocks (Xiphopenaeus kroyeri
Heller, 1862) from southeastern Brazil: a stable
isotope approach
Keltony de Aquino Ferreira 1,
Leandro Rabello Monteiro 2 & Ana Paula
Madeira Di Beneditto 3
1,2,3 Universidade Estadual
do Norte Fluminense Darcy Ribeiro, CBB, Laboratório de Ciências Ambientais, Av. Alberto Lamego
2000, Campos dos Goytacazes, RJ, 28013-600, Brazil.
1 keltony.aquino@yahoo.com.br, 2
lrmont@uenf.br, 3 anadibeneditto@gmail.com (corresponding
author)
Editor: Mandar Paingankar,
Government Science College, Gadchiroli, India. Date
of publication: 26 June 2020 (online & print)
Citation: Ferreira, K.A., L.R. Monteiro
& A.P.M. Di Beneditto (2020). The niche of shrimp stocks (Xiphopenaeus kroyeri
Heller, 1862) from southeastern Brazil: a stable
isotope approach. Journal of Threatened Taxa 12(9): 16173–16176. https://doi.org/10.11609/jott.5961.12.9.16173-16176
Copyright: © Ferreira et al. 2020. Creative Commons Attribution
4.0 International License. JoTT allows unrestricted use, reproduction, and
distribution of this article in any medium by providing adequate credit to the
author(s) and the source of publication.
Funding: Conselho Nacional
de Desenvolvimento Científico
e Tecnológico - CNPq
(301.259/2017-8), Fundação Carlos Chagas
Filho de Amparo à Pesquisa do Estado do Rio de
Janeiro - FAPERJ (E-26/202.770/2017, E-26/210.064/2018, E-26/210.883/2016), Coordenação de Aperfeiçoamento de
Pessoal de Nível Superior
(CAPES) – Financial code 001.
Competing interests: The authors
declare no competing interests.
Acknowledgements: We are grateful to Dr. Marcelo Gomes de Almeida for the stable isotopes
analysis.
The penaeid shrimps are important
targets in crustacean fisheries worldwide.
The species Xiphopenaeus kroyeri Heller, 1862, known as the Atlantic Seabob Shrimp, is a penaeid species with continuous
distribution in coastal waters along the western Atlantic Ocean, from 36°N to
30°S, and their stocks are highly exploited by marine coastal fisheries (FAO
2018). In Brazil, this is the second
most important species of crustacean in fisheries landings (Boos et al. 2016).
Stable isotopes of carbon (13C)
and nitrogen (15N) are applied as chemical proxies to provide
complementary data on animals’ trophic ecology (Fry 2008). Niche differentiation is the process by which
species evolve different forms of food sources use (MacArthur 1984). Layman et al. (2007) introduced metrics from
ecomorphological approaches to summarize quantitative information from stable
isotopes data. Later, Jackson et al.
(2011) developed a Bayesian framework for these metrics comparisons, allowing
robust inferences regarding isotopic niche of animal species. Thus, stable isotopes provide quantitative
information about the consumer isotopic niche, which is associated with its
feeding ecology and ecological niche in the environment.
This study evaluated the niche
dimensions of X. kroyeri (Image 1) from four
stocks in southeastern Brazil through stable isotopes
determinations. We hypothesize that the
isotopic niche is similar among the four stocks because this shrimp is an
omnivorous consumer with high feeding plasticity, consuming a broad spectrum of
food sources that are abundant in its home range, such as primary sources and
small animals from both benthic environment and water column (Willems et al.
2016).
The shrimps were sampled in four
fishing areas from Espírito Santo and Rio de Janeiro
States, southeastern Brazil: Vitória (-20.51S &
-40.50W), Anchieta (-20.80S & -40.63W), Atafona (-21.61S & -41.00W), and Farol
de São Tomé (-22.03S & -41.03W) (Figure 1).
In June 2017, 120 individuals were sampled in the local fishing market
from each fishing area, totalling 480 individuals. The abdominal muscle of each individual was
removed and stored in a dry sterile vial, frozen (-20oC),
freeze-dried and homogenized using mortar and pestle. Samples containing 0.4g of muscle (dry
weight) of each individual were analysed for Carbon and Nitrogen isotopic
determination. The stable isotopes
ratios (δ13C and δ15N) of each shrimp was determined
using a Delta V Advantage mass spectrometer (Thermo
Scientific, Germany) coupled to an elemental analyser in Laboratório
de Ciências Ambientais from
Universidade Estadual do
Norte Fluminense Darcy Ribeiro. The reference values for Nitrogen and Carbon
stable isotopes were atmospheric Nitrogen and Pee Dee Belemnite (PDB),
respectively. Samples were analysed
using analytical blanks and urea analytical standards (IVA Analysentechnik-330802174;
CH4N2O Mw = 60, C = 20%, N = 46%), using certified
isotopic compositions (δ13C = -39.89‰ and δ15N =
-0.73‰). Analytical control was done for
every 10 samples using a certified isotopic standard (Elemental Microanalysis
Protein Standard OAS): δ13C = -26.98‰ and δ15N =
+5.94‰. Analytical reproducibility was
based on triplicates for every 10 samples: ± 0.3‰ for δ15N and ±
0.2‰ for δ13C.
Quantitative metrics of the
isotopic niche based on individuals’ position in δ13C-δ15N
bi-plot space were estimated according to Layman et al. (2007) and Jackson et
al. (2011). The metrics were calculated
using Stable Isotope Bayesian Ellipses in R (SIBER - Jackson et al. 2011; R
Core Team 2020). The first two metrics
represent the stocks trophic diversity, and the last two represent the stocks
trophic redundancy, or the relative position of individuals to each other
within their respective isotopic niches. The standard ellipse area (SEA) is the
isotopic niche width of a given stock, based on bivariate distribution ellipses
for each stock and sized to include 40% of the data subsequently sampled. The mean distance to centroid (CD) is the
mean Euclidian distance from each individual to stock centroid (mean δ15N
and δ13C), which provides average level of trophic diversity. The mean nearest neighbour distance (MNND) is
the mean Euclidian distance from each individual to the nearest neighbour in δ13C–δ15N
bi-plot space, indicating similarity in trophic ecology within stocks. The standard deviation of nearest neighbour
distance (SDNND) is a measure of stock uniformity in δ13C–δ15N
bi-plot space, or the evenness of individuals’ distribution within stocks. One-way ANOVA evaluated differences among
stocks considering CD and MNND metrics, as these are means. SDNND metric was compared using F-ratio tests
because it is a standard deviation. The
statistical analyses were done in the R program (R Core Team 2020).
The X. kroyeri
stocks from Espírito Santo State (Vitória and Anchieta) had highest SEA values when compared to stocks
from Rio de Janeiro State (Atafona and Farol de São Tomé) (Table 1, Figure 2); and also highest
values for the average level of trophic diversity (CD) (ANOVA, F = 7.49,
df = 3, p = 6.53e-05) (Table 1). The MNND values that show the similarities in
trophic ecology within stocks were low, and did not differ among the stocks
(ANOVA, F = 1.74, df = 3, p =
0.16); however, higher values were recorded for stocks from Rio de Janeiro
State (Table 1). Individuals’
distribution in the isotopic niche space revealed the highest and the lowest
trophic uniformity (SDNND) for shrimps from Atafona
and Anchieta stocks, respectively (Table 1). Comparisons using F tests showed
significant results (p < 0.01), except for the comparison between
Vitória and Farol de São Tomé stocks (p =
0.15).
The results refuted the
hypothesis that the four X. kroyeri stocks
have similar isotopic niche width because of the high feeding plasticity of
this species. Shrimp stocks from Espírito Santo State (Vitória and Anchieta)
had highest trophic diversity (SEA and CD metrics), indicating greater variety
of food sources and wider utilization of the available food sources. The shrimps from Rio de Janeiro State (Atafona and Farol de São Tomé)
had highest trophic redundancy (MNND and SDNND metrics), revealing a more
homogeneous dietary pattern. In general,
shrimps have high feeding plasticity, and variations in diet composition and in
the amount ingested can occur among species, genders, maturity stages and
seasons, even on a small spatial scale (Carnevali et
al. 2012; Gutiérrez et al. 2016). The
isotopic composition of the animal tissues derives from the ingested food
sources and fractionation processes in these tissues, and the carbon and
nitrogen isotopic values can differ both spatially and among the food sources
ingested by the consumer (Fry et al. 2003; Fry 2008). Thus, the composition of food sources and
availability in each fishing area might explain the variations among the X. kroyeri stocks regarding their isotopic niches. Further studies on the local feeding ecology
of this species, such as the study conducted by Willems et al. (2016) off the
coast of Suriname, are recommended to confirm this assumption.
In Suriname, a combination of
stomach content and stable isotope analyses from X. kroyeri
individuals in different life stages showed that hyperbenthic crustaceans,
benthic microalgae and offshore sedimentary organic matter were important food
sources, with benthic microalgae contributing up to 64% to the overall diet for
all life stages, however, an ontogenetic diet shift was recorded, with adult
shrimps positioned higher in the food chain (δ15N more enriched),
preying on larger benthic organisms (Willems et al. 2016). The isotopic data of
the four X. kroyeri stocks from southeastern Brazil can be combined with future stomach
content analysis to verify and compare the feeding preference in this region to
the data from Suriname.
We can state that the isotopic
niche approach allowed the discrimination of X. kroyeri
stocks distributed at 200S (fishing areas of Espírito
Santo State) and 210S–220S (fishing areas of Rio de
Janeiro State). Recognizing the seafood
origin allows determining the fishers’ fidelity to a given fishing area
(geographical origin), besides developing inferences on seafood quality from
the environmental quality (Ortea & Gallardo
2015). The results will be
helpful to assist fisheries management, delimitating the fishing area of local
vessels and helping track the origin of the shrimps commercialized in local
markets.
Table 1. Quantitative metrics of
isotopic niche of Xiphopenaeus kroyeri stocks from Espírito
Santo and Rio de Janeiro states.
|
Stocks/ Fishing areas |
SEA‰² |
CD |
MNND |
SDNND |
||
|
|
LQ |
Med |
UQ |
|
|
|
|
Espírito Santo State |
|
|
|
|
|
|
|
Vitória |
0.59 |
0.63 |
0.67 |
0.66 |
0.07 |
0.10 |
|
Anchieta |
0.41 |
0.44 |
0.47 |
0.51 |
0.08 |
0.27 |
|
Rio de Janeiro State |
|
|
|
|
|
|
|
Atafona |
0.24 |
0.25 |
0.27 |
0.37 |
0.04 |
0.05 |
|
Farol de São Tomé |
0.25 |
0.26 |
0.28 |
0.36 |
0.04 |
0.12 |
CD—distance to centroid |
MNND—mean nearest neighbour distance | SDNND—standard deviation of nearest
neighbour distances | SEA—standard ellipse area | LQ—lower quartile | UQ—upper quartile |
Med—Median.
For
figures & image - - click here
References
Boos, H.,
R.C. Costa, R.A.F. Santos, J. Dias-Neto, E.
Severino-Rodrigues, L.F. Rodrigues, F. D’Incao,
C.T.C. Ivo & P.A. Coelho (2016). Avaliação dos camarões peneídeos (Decapoda: Penaeidae), pp. 300–317. In: Pinheiro, M. & H. Boos
(eds.). Livro vermelho
dos crustáceos do Brasil: Avaliação 2010–2014. Sociedade
Brasileira de Carcinologia,
Porto Alegre, 466pp.
Carnevali, R.P., P.A. Collins & A.S.G. Poi de Neiff (2012). Trophic ecology of the freshwater
prawn, Pseudopalaemon bouvieri
(Decapoda: Palaemonidae) in
Northeastern Argentina: with remarks on population
structure. Revista de Biología Tropical 60: 305–316.
FAO (2018). The state
of world fisheries and aquaculture 2018 - Meeting the sustainable development
goals. FAO, Rome, 210pp. http://www.fao.org/3/i9540en/i9540en.pdf
Fry, B.
(2008). Stable Isotope Ecology. Springer-Verlag, New York, 308pp.
Fry, B.,
D.M. Baltz, M.C. Benfield, J.W. Fleeger, A. Gace,
H.L. Haas & Z.J. Quinones-Rivera (2003). Stable
isotope indicators of movement and residency for brown shrimp (Farfantepenaeus aztecus)
in coastal Louisiana Marshscapes. Estuaries 26:
82–97. https://doi.org/10.1007/bf02691696
Gutiérrez,
J.C.S., J.T. Ponce-Palafox, N.B. Pineda-Jaimes, V.
Arenas-Fuentes, J.L. Arredondo-Figueroa & J.L. Cifuentes-Lemus (2016). The
feeding ecology of penaeid shrimp in tropical lagoon-estuarine systems. Gayana 80: 16–28. https://doi.org/10.4067/s0717-65382016000100003
Jackson,
A.L., R. Inger, A.C. Parnell & S. Bearhop (2011).
Comparing isotopic niche widths among and within communities: SIBER –
Stable Isotope Bayesian Ellipses in R. Journal of Animal Ecology 80:
595–602. https://doi.org/10.1111/j.1365-2656.2011.01806.x
Layman,
C.A., D.A. Arrington, C.G. Montana & D.M. Post (2007). Can stable
isotope ratios provide for community-wide measures of trophic structure? Ecology
88: 42–48. https://doi.org/10.1890/0012-9658(2007)88[42:csirpf]2.0.co;2
MacArthur, R.H. (1984). Geographical Ecology:
Patterns in the Distribution of Species. Princeton, Princeton University
Press, 269pp.
Ortea, I. &
J.M. Gallardo (2015). Investigation of production method,
geographical origin and species authentication in commercially relevant shrimps
using stable isotope ratio and/or multi-element analyses combined with chemometrics: An exploratory analysis. Food chemistry
170: 145–153. https://doi.org/10.1016/j.foodchem.2014.08.049
R Core Team
(2020). R: A language and environment for statistical computing. Version 3.6.3.
R Foundation for Statistical Computing. Available at:
https://www.R-project.org/
Willems, T.,
A. De Backer, T. Kerkhove, N.N. Dakriet,
M. De Troch, M. Vincx & K. Hostens
(2016). Trophic ecology of Atlantic sea-bob shrimp Xiphopenaeus
kroyeri: Intertidal benthic microalgae support
the subtidal food web off Suriname. Estuarine Coastal and Shelf Science
182: 146–157. https://doi.org/10.1016/j.ecss.2016.09.015