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Local trade, spatial occurrence and conservation of hypostomus soniae (siluriformes, loricariidae), an ornamental fish endemic to the tapajos river, Brazil

Abstract

Hypostomus soniae is a small sized armored catfish endemic to the Tapajos River basin and ranked as one of the most exploited ornamental fish in the Santarem export marketplace. This study aims to evaluate distributional patterns of Hypostomus soniae and contribute to the species conservation in the face of development of the ornamental fish trade in the Amazon region. We compiled data associated with geographic coordinates in public repositories, supplemented with original field records. We compared our data to published records in the literature and museum collections to check for accuracy. To investigate the fishery and commercialization of H. soniae, we conducted interviews with ornamental fish stakeholders from the local trade. We also made direct observations in the fishing sites and export facilities in Santarem. A cluster analysis of the geolocation data was carried out to explore the spatial distribution patterns. The volume of captures and exportation of H. soniae decreased during the period 2020-2023. The occurrence of H. soniae was associated with annual rainfall ranging from 2,000 mm to 2,500 mm and concentrated in two municipalities of the State of Mato Grosso and two of the Para State. The species distribution area has been threatened, unfortunately, by fishermen who do not respect the laws that support artisanal fishing in the Amazon.

Key words
Amazon; Distribution; Geolocation; Investigate; Kernel

INTRODUCTION

The armored catfish (Loricariidae, Siluriformes) is a large and complex group of fish from the Neotropics. The family Loricariidae covers more than a thousand species assembled in six subfamilies: Lithogeneinae, Delturinae, Rhinelepinae, Loricariinae, Hypoptopomatinae and Hypostominae (Fricke et al. 2023FRICK R, ESCHMEYER WN & FONG JD. 2023. Catalog of fishes: Genera, species references 1: 1-14.). Loricariids inhabit a wide range of habitats from low elevations to upland rivers situated 3,000 meters above sea level (Nelson 2006NELSON JS. 2006. Fishes of the world. 4th ed., John Wiley & Sons: New Jersey: 1-622.), display nocturnal activity foraging in the riverbed (Soares et al. 2008SOARES MGM, COSTA EL, SIQUEIRA SOUZA FK, ANJOS HDB, YAMAMOTO KC & FREITAS CEC. 2008. Peixes de lagos do Médio Rio Solimões. Rev Inst Piatam: 1-176.), and have a varied trophic ecology being detritivore, algivorous, carnivore, omnivore and xylophagous (Jesus 2020JESUS TS. 2020. Hábitos alimentares e relações morfológicas de espécies de Loricariidae (Actinopterygii:Siluriformes) da região da volta grande do rio Xingu, Para, Brasil (Master dissertation, Instituto Nacional de Pesquisas da Amazonia), 59 p. Programa de Pós- graduação em Água Doce e Pesca Interior, Instituto Nacional de Pesquisas da Amazonia, Manaus. (Unpublished).).

Loricariid species are characterized with a body recovered by dermal plates and a suction cup-like ventral; however, this fish group displays high diversity in morphology, coloration and behavior (Lujan et al. 2012LUJAN NK, WINEMILLER KO & ARMBRUSTERJ. W. 2012. Trophic diversity in the evolution and community assembly of loricariid catfishes. BMC Evol Biol 12: 2-12.). Such diverse trait combinations, and their exotic appearance, have made catfish one of the main products in the international freshwater ornamental fish industry (Sousa et al. 2021SOUSA LM, LUCANUS O, ARROYO-MORA JP & KALACSKA M. 2021. Conservation and trade of the endangered Hypancistrus zebra (Siluriformes, Loricariidae), one of the most tracked Brazilian fish. Glob Ecol Cons 27: 1-23., Maciel et al. 2022MACIEL LAM, GUIMARAES EC, GUIMARAES KLA, BRITO OS & RODRIGUES LRR. 2022. Um olhar sobre a bioeconomia da pesca ornamental no rio Tapajós: Peixes e pescadores da vila de Pimental. In: 2° Congresso Brasileiro de Biodiversidade e Biotecnologia da Amazonia. 2, Belém -PA. ISBN 978-65-89463-25-2.).

The ornamental fish industry is a large enterprise that moves billions of dollars worldwide and sells more than 2,500 species, more than half coming from freshwater environments (Dey 2016DEY VK. 2016. The Global Trade in Ornamental Fish. Inf Inter 4: 52-55.). In Brazil, this economic sector is supported by fisheries with wild fish stocks, and the Amazon basin is the largest producing region (Araujo et al. 2017ARAUJO JG, SANTOS MAS, REBELLO FK & ISAAC VJ. 2017. Cadeia comercial de peixes ornamentais do Rio Xingu, Para, Brasil. Bol Inst Pesca 43: 297-307.).

Brazilian authority regulates the capture of native species for commercial use in ornamental fish trade, a measure that a priori favors the conservation of natural stocks. However, the economic viability and sustainable use of fishery resources is threatened by impacts from degradation of the freshwater environment, overfishing, biopiracy (Biondo & Burki 2020BIONDO MV & BURKI RP. 2020. A Systematic Review of the Ornamental Fish Trade with Emphasis on Coral Reef Fishes—An Impossible Task. Animals 10: 1-19., Sousa et al. 2021SOUSA LM, LUCANUS O, ARROYO-MORA JP & KALACSKA M. 2021. Conservation and trade of the endangered Hypancistrus zebra (Siluriformes, Loricariidae), one of the most tracked Brazilian fish. Glob Ecol Cons 27: 1-23.).

The Amazon super basin has the greatest diversity of freshwater fish (Jézéquel et al. 2020JÉZÉQUEL C ET AL. 2020. A database of freshwater fish species of the Amazon Basin. Scientific Data 7(1): 96.) which makes this region strategic and highly relevant for the global ornamental fish market. In the Amazon aquatic landscape, the spatial distribution of species diversity is largely heterogeneous and highly complex, however Endemic Amazonian Fish Areas (EAFA) are clearly indicated (Dagosta et al. 2020DAGOSTA FCP, ZANATA AM, OHARA WM & OYAKAWA OT. 2020. A newrheophilic South American darter (Crenuchidae:Characidium) from the rio Juruena basin, Brazil, with comments on morphological adaptations to life in fast-flowing waters. J Fish Biol 97: 1343-1353.). The largest volumes of ornamental loricariid catches come from the Xingu, Tapajos and Tocantins rivers (Camargo et al. 2012CAMARGO M, JUNIOR G & PY-DANIEL LR. 2012. Acaris ornamentais do médio Rio Xingu. ISBN 978-85-909319-1-1., Araujo et al. 2017ARAUJO JG, SANTOS MAS, REBELLO FK & ISAAC VJ. 2017. Cadeia comercial de peixes ornamentais do Rio Xingu, Para, Brasil. Bol Inst Pesca 43: 297-307., Sousa et al. 2018a, Maciel et al. 2022MACIEL LAM, GUIMARAES EC, GUIMARAES KLA, BRITO OS & RODRIGUES LRR. 2022. Um olhar sobre a bioeconomia da pesca ornamental no rio Tapajós: Peixes e pescadores da vila de Pimental. In: 2° Congresso Brasileiro de Biodiversidade e Biotecnologia da Amazonia. 2, Belém -PA. ISBN 978-65-89463-25-2.), where the fishing grounds are located in the EAFA Brazilian shield (Dagosta et al. 2020DAGOSTA FCP, ZANATA AM, OHARA WM & OYAKAWA OT. 2020. A newrheophilic South American darter (Crenuchidae:Characidium) from the rio Juruena basin, Brazil, with comments on morphological adaptations to life in fast-flowing waters. J Fish Biol 97: 1343-1353.).

The human pressure linked to the ornamental fish trade and other drives such as environment disturbance and lack of biological knowledge can potentially move a species toward extinction (Hurd et al. 2016HURD LE, SOUSA RG, SIQUEIRA-SOUZA FK, COOPER GJ, KAHN JR & FREITAS CE. 2016. Amazon floodplain fish communities: habitat connectivity and conservation in a rapidly deteriorating environment. Biol Conser 195: 118-127., Biondo & Burki, 2020). An illustrative case is the critically endangered Hypancistrus zebra, which is endemic to a restricted sector of the Xingu River and overexploited by the ornamental fish trade (Sousa et al. 2021SOUSA LM, LUCANUS O, ARROYO-MORA JP & KALACSKA M. 2021. Conservation and trade of the endangered Hypancistrus zebra (Siluriformes, Loricariidae), one of the most tracked Brazilian fish. Glob Ecol Cons 27: 1-23.).

The Xingu-Tapajos region has been recognized as a priority area to support the sustainable use of ornamental loricariids for the freshwater aquarium hobby industry. The adoption of conservation policies and scientific research converging with bioeconomic planning have contributed to sustainability of the ornamental fisheries in the Amazon basin (Ramos et al. 2015RAMOS FM, ARAUJO MLG, PRANG G & FUJIMOTO RY. 2015. Ornamental fish of economic and biological importance to the Xingu River. Braz J Biol 75: 95-98.).

Animal movement is one of the most remarkable biological phenomena and hence deserves strong scientific interest (Bronmark et al. 2013BRONMARK C, HULTHEN K, NILSSON A & SKOV C, Hansson LA, Brodersen J, CHAPMAN B. 2013. There and back again: Migration in freshwater fishes. Cana Jour of Zoo: 92: 1-13.). Fish movement and spatial distribution along the Amazon basin remain poorly understood (Hurd et al. 2016HURD LE, SOUSA RG, SIQUEIRA-SOUZA FK, COOPER GJ, KAHN JR & FREITAS CE. 2016. Amazon floodplain fish communities: habitat connectivity and conservation in a rapidly deteriorating environment. Biol Conser 195: 118-127., Dagosta & Pinna 2021DAGOSTA FCP & PINNA M. 2021. Two new catfish species of typically Amazonian lineages in the Upper Rio Paraguay (Aspredinidae: Hoplomyzontinae and Trichomycteridae: Vandellinae) with a biogeografic discussion. Pap. Avulsos Zool 61: 1-23.). Analyses of fish spatial distribution in threatened areas, such as the endemic regions in the Tapajos, Juruena and Teles Pires (Buckup & Santos 2010BUCKUP PA & SANTOS GM. 2010. Ictiofauna da Ecorregiao Xingu-Tapajós: fatos e perspectivas. Boletim Sociedade Brasileira Ictio 98: 3-9., Dagosta & Pinna 2021DAGOSTA FCP & PINNA M. 2021. Two new catfish species of typically Amazonian lineages in the Upper Rio Paraguay (Aspredinidae: Hoplomyzontinae and Trichomycteridae: Vandellinae) with a biogeografic discussion. Pap. Avulsos Zool 61: 1-23.) are relevant to support management strategies, as well as to point out the need for future revisions in the national and global lists of endangered species (Assumpcao et al. 2017).

In this study we investigated the occurrence records, spatial distribution, and trade of Hypostomus soniae Hollanda Carvalho & Weber, 2004CARVALHO HP & WEBER C. 2014. Five new species of the Hypostomus cochliodon group (Siluriformes: Loricariidae) from the middle and lower Amazon System. Rev Sui Zoo 111: 953-978. (Loricariidae, Hypostominae), a species endemic to Tapajos River basin and exploited as ornamental fish. This species is popularly named as violet plecos and commercially coded as L-137. Santarem is the exportation (Maciel et al. 2022MACIEL LAM, GUIMARAES EC, GUIMARAES KLA, BRITO OS & RODRIGUES LRR. 2022. Um olhar sobre a bioeconomia da pesca ornamental no rio Tapajós: Peixes e pescadores da vila de Pimental. In: 2° Congresso Brasileiro de Biodiversidade e Biotecnologia da Amazonia. 2, Belém -PA. ISBN 978-65-89463-25-2.). Between the years 2013-2016 more than 5000 individual units of H. soniae were exported from this trade hub (Sousa et al. 2018bSOUSA ALP. 2018a. Aspectos socioeconômicos e identificação molecular de peixes ornamentais da família Loricariidae (Siluriformes) comercializados em Santarém-PA, Doctoral dissertation, Universidade Federal do Oeste do Para, 72 p.).

MATERIALS AND METHODS

Description of study species

Hypostomus soniae Hollanda Carvalho & Weber 2004 (Siluriformes, Loricariidae) was described from Tapajos River between Vila Nova and Urua, municipality of Itaituba and is considered endemic to the Tapajos River basin (Figure 1). The species is allocated in the Hypostomus cochliodon group and distinguished by its particular color pattern without spots, sometimes with darker longitudinal stripes (versus spotted pattern, without stripes), its particular long and slightly curved adipose fin spine, the standard length varied from 76.4 to 145.8 mm in the type of material.

Figure 1
Map of the occurrence area of Hypostomus soniae Hollanda-Carvalho & Weber 2004.

The species is endemic and restricted to a narrow distribution along the Tapajos River, where its range is enclosed in the Brazilian shield endemicity area reaching parts of the Brazilian Cerrado, a well-known world’s biodiversity hotspot (Myers et al. 2000MYERS N, MITTERMEIER RA, MITTERMEIER CG, FONSECA GAB & KENT J. 2000. Biodiversity hotspots for conservation priorities. Nature 403: 853-858.). This region has been disturbed by large scale infrastructure projects, artisanal gold mining and the increase of agricultural frontiers, which inevitably affects the fish populations due to aquatic pollution loss of habitats and genetic connectivity (Pelicice et al. 2017PELICICE FM ET AL. 2017. Neotropical freshwater fishes imperiled by unsustainable policies. Fish 18: 19-33.).

Local trade data analysis

We investigated the fishery and local commercialization of H. soniae from Tapajos River, Para State. Data about ornamental fishery and economic aspects of the local trade were collected from interviews with artisanal fishermen residing in the Village of Pimental (4° 34 ‘5.90 “ S and 56° 15’ 44.40” W) and ornamental fish exporters based in Santarem city. All the participants (n=16) were previously informed about the research and gave their voluntary consent (TCLE).

This research was approved by the Ethical Committee at Federal University of Western Para (Process Number 5.476.648). Additional information was obtained by direct observations during field trips to the Village of Pimental (11-15, July 2021, LAMM), and visits to fish management facilities in the cities of Itaituba and Santarem. Data on local trade of Hypostomus soniae, during 2020-2023, were obtained from documental analysis in the Secretary of Environment and Sustainability (SEMAS), System of Fauna, Aquaculture and Fishery (SISFAP), from Para State.

Spatial data acquisition

Records of the species occurrence were compiled from a public digital database, Information System on Brazilian Biodiversity (SIBBR 2021SIBBR. 2021. Sistema de Informação sobre a Biodiversidade Brasileira, disponível em: https://www.sibbr.gov.br/, acesso em junho de 2023.
https://www.sibbr.gov.br/...
). Additional geographic information was recovered from the field expeditions conducted by the research team (LRRR and LAMM) and was extracted from the scientific literature, considering the geographic coordinates of the collection areas of the target species. A database of the geographic information system for H. soniae is accessible in the Supp. file Table I.

Table I
Example of variables which compose the Information System on Brazilian biodiversity.

Spatial data analysis

To support the analysis of the distribution of this species, an identification of abiotic characteristics associated with the areas of occurrence of the species was carried out, mainly in terms of climate typology, rainfall, and air temperature, making a cut in the database of (Martorano et al. 2017MARTORANO LG, VITORINO MI, SILVA BPPC, MORAES JRSC, LISBOA LS, SOTTA ED & REICHARDT K. 2017. Climate conditions in the eastern amazon: Rainfall variability in Belem and indicative of soil water deficit. Afr J Agric Res 12: 18011-810., Xavier et al. 2016XAVIER AC, KING CW & SCALON BR. 2016. Daily gridded meteorological variables in Brazil (1980-2013). Inter J Clim 36: 2644-2659.).

The occurrence points were plotted using geoprocessing techniques identified by their respective geographic coordinates. From the geolocations, the data were tabulated according to the following procedures: Geolocation of the species; Plotting occurrence points using ArcGIS 10.6; Access to georeferenced geographic database usage bases, made available by the user of the Institute of Geography and Statistics (IBGE), using the shapefile format; and use of the Kernel density technique to identify occurrence patterns. Kernel Density Estimator (KDE) analysis, presented by (Parzen 1962PARZEN E. 1962. On the estimation of a probability density function and mode. Ann Math Stat 33: 1065-1076.) was adopted because it allows estimating densities based on local information based on non-parametric data models using the probability density function of a random variable.

It uses matrices to induce functions from the structural information contained in the data, considering only the width of the Kernel function, without the need for a priori assumptions about the shape of the generating function. Thus, density estimation allows data smoothing with inferences about populations, based on a finite data sample, where (x1, x2, …, xn) represent a sample of an independent and identically distributed random variable with a density f unknown. The density estimate by Kernel is expressed by the following equation 1:

( x t ) = 1 n K ( x t x i )
N h i = 1

Where: N is the number of samples, h is the Kernel smoothing parameter and K (xt , xi) is the Kernel operator, whose integral R K(u)du must be unitary. The function argument K is actually the point where you want to estimate, since the samples xi (i = 1 . . . N) are fixed and provided to the model.

RESULTS AND DISCUSSION

Data from interviews with ornamental fishermen in the region show that fishing for H. soniae occurs at several fishing sites along the Tapajos River between the cities of Itaituba and Jacareacanga in Para State. Fish are collected manually by experienced fishermen using diving techniques.

During the high season, the fishermen reported staying up to six days a week at the sites where they catch the species, returning to the village only at weekends. On average, they fish for 6 hours a day, but they don’t follow a fixed schedule because each fisherman plans his actions according to the specifics of the fishing area. They were unable to say how many specimens they caught each day.

The fishery of H. soniae occurs at several fishing sites along the Tapajos River between the cities of Itaituba and Jacareacanga in Para State. Fishes are collected manually by experienced fishermen using diving techniques. The fishing season runs from April to November and the price of each individual unit varies by body length small sized (6 cm TL) is sold for R$ 3,00 (Real) and medium sized (up to 9 cm TL) is sold for R$ 4,00, from the fishermen to the local exporters based in Santarem. Large sized individuals (> 9 cm TL) usually are not collected, aiming to preserve species reproduction.

In the period of 2020-2023, 1938 individuals of H. soniae were commercialized from anglers to exporters based in Santarem, while 1245 were exported from Santarem to international trade. We observed a clear reduction in the volume of captures and commercial transactions of H. soniae in the period of study. This could be a result of decreasing demands from ornamental fish clients; however, an alternative hypothesis could be a real decline in stock populations, which should be investigated in further studies.

For the period of the pandemic in the region, more precisely in the years 2020 and 2021, the fishermen pointed out that the main impacts of the pandemic on fishing activity were the paralysis of the activity, spending around 5 months without fishing, as well as difficulties in transporting and disposing of the fish, and a decrease in sales due to flight restrictions.

Also for the same period, information obtained from companies in the aquarium sector points to the restriction of flights and flows between cities imposed by the pandemic as the main obstacle to the sale of ornamental fish in the region, followed by an increase in the price of items used in aquarium production.

The village of Pimental is an important hub for the H. soniae fishery and represents the main hub for supplying ornamental fish from the Tapajos River to exporters based in Itaituba and Santarem cities. The ornamental fishery carried out in the Tapajos River meets a demand from the foreign market, being responsible for the direct export of this natural resource to at least 16 countries, mainly in the Asian continent, where China is the largest buyer of ornamental fish from Brazil (Sousa et al. 2018SOUSA ALP, MACIEL LAM & RODRIGUES LRR. 2018b. Estudo da comercialização de peixes ornamentais da família Loricariidae (Siluriformes) em Santarém/PA. PUBVET 12: 1-7.).

The spatial analysis of H. soniae occurrences revealed that most records were associated with areas with predominance of climatic typologies Am3 and Aw3.The species predominates in areas with annual rainfall ranging from 2,000 mm to 2,500 mm and average monthly values below 60 mm, fitting into these two climatic typologies (Martorano et al. 1993MARTORANO LG, NECHET D & PEREIRA LC. 1993. Tipologia climática do Estado do Para: Adaptação do método de Köppen. Bol Geogr Teorética 23: 45-46. and Martorano et al.2017).

Evaluating the locations of H. soniae occurrences using the annual rainfall base, confirms that the georeferenced information pointed to concentrations of the species in areas where rainfall throughout the year varies between 2,000 mm and 2,500 mm, in the States of Mato Grosso and Para.

In Mato Grosso, the municipalities Alta Floresta and Paranaita (Mato Grosso) and Itaituba and Jacareacanga (Para) showed the highest occurrences of H. soniae. It is not clear if this abundance pattern is resulted from spatial distribution of the species habitat. It is possible that there is bias associated with records originated from ornamental fishery efforts (Figure 2).

Figure 2
Climatic typology, annual rainfall and Kernel density map of Hypostomus soniae concentrations in the Tapajos River basin indicating the places with predominance of the violet acari.

The Kernel density analysis showed that H. soniae geographic data present an overestimation, when negative values are compared. The estimates present high precision close to 0.796 based on the 1:1 line, showing that the more data on occurrences of this species, the more sensitive the density estimator is in pointing out the probability of existence of this species in the study area (Figure 3).

Figure 3
Statistical analysis showing the adjustments of samples of occurrences of the species Hypostomus soniae.

Further field research is needed to validate if the occurrence gaps represent either the species absence or lack of biodiversity knowledge. Short spatial scale movements are associated with conditions of shelter, foraging, territory guarding and dispersal because they are ecological factors that limit the scale of dynamic mobility of populations and metapopulations and their persistence in fragmented environments (Comte & Olden 2018COMTE L & OLDEN JD.2018. Fish dispersal in flowing waters: A synthesis of movement- and genetic-based studies. Fish and Fish 19: 1063-1077.).

Limitations regarding occurrence data were also pointed out by (Ramos et al. 2019RAMOS FM ET AL. 2019. Feed management and stocking density of the endangered wild zebra pleco: Implications for captive breeding. Aquac Res 50(9): 2437-2443.) who identified the predominance of loricariids (plecos) and characids (piabas) for ornamental use, indicating that these two families require accurate information regarding taxonomic aspects, which is hampered by a small number of group specialists with skill to identify this ichthyofauna, at the species level. Geographic, hydrological, and climatic peculiarities are the main factors that contribute to the occurrence of the studied species.

A detailed analysis of biophysical characteristics in the Tapajos River basin and its tributaries can help indicate new potential areas of occurrence for H. soniae. We emphasize that the mapping of the areas of occurrence and patterns of population density are relevant information to support governance and sustainability measures for Brazilian ornamental fisheries. For instance, the areas in Para and Mato Grosso States that retain largest occurrences of H. soniae could be considered suitable for domestication programs and reproductive management of the species.

Ornamental fishery driven by anthropic pressure for exotic and rare species combined with the lack of biological information about the commercialized species can pose an effective threat to wild populations (Junior et al. 2009JUNIOR JR ET AL. 2009. Sobre a pesca de peixes ornamentais por comunidades do rio Xingu, Para - Brasil: relato de caso. Bol Inst Pes 35: 521-530., Tavares 2020TAVARES DM. 2020. Espécies de peixes ornamentais capturados pela pesca no estado do Amapá. Macapá: Embrapa Amapá: 1-15.). An equitable use and conservation of H. soniae deserves attention from both the government sector and the ornamental fish trading stakeholders.

CONCLUSIONS

Hypostomus soniae has been exploited annually in the Tapajos River for at least one decade. All trade in ornamental fish that has been exported abroad comes from points of sale in the cities of Santarem and Itaituba. The village of Pimental is the main hub of ornamental fish landing in the upper Tapajos, where a price for an individual unit of H. soniae is R$ 3,00 - 4,00.

The spatial occurrences of Hypostomus soniae is associated with areas of annual rainfall ranging from 2,000 mm to 2,500 mm and concentrated in two municipalities of the State of Mato Grosso and two of the Para State. The pressure exerted by anglers compromises the distribution area of the species. These anglers represent threats to the sustainability of ornamental fishing and to the conservation of the species.

ACKNOWLEDGMENTS

The authors thank to Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES) for the scholarship granted to student Denison Lima Correa. As well as to Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq) for granting a scholarship to student Luan Aercio Melo Maciel, doctoral students of the Postgraduate Program in Biodiversity of the BIONORTE network and to Graduate Program in Society, Nature and Development (PPGSND/UFOPA), respectively. LRRR was supported by CAPES - Program PDPG Amazonia Legal, Project “ Consolidation of Postgraduate Studies in Health Sciences with a focus on Biotechnology and Therapeutic Innovation for Health Care “ (Process 88887.510169/2020-00 - SCBA).

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Publication Dates

  • Publication in this collection
    27 May 2024
  • Date of issue
    2024

History

  • Received
    10 Aug 2023
  • Accepted
    04 Mar 2024
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