MARINE AND FISHERY SCIENCES 35 (2): 165-180 (2022)
https://doi.org/10.47193/mafis.3522022010501
ABSTRACT. Of particular concern in commercial fishing catch is 'size bycatch', i.e., the death
of early stages of resources that would reach a marketable value when they turn into adults. This
event is frequently associated with trawling because of the lower size selectivity of this gear as com-
pared to gillnets. However, this is expected when small-scale fisheries (SSF) employ gillnets simul-
taneously in setnets + driftnets that mix multiple mesh sizes. This work analyzes fishing captures
and compares characteristics of fish catch from gillnets and trawlers with respect to size at first mat-
uration, legal size of capture, and expected discards. Data were obtained from 2007-2021 for SSF
in Southern Brazil. A total of 112 fish species were represented in the data. Gillnets exploited fewer
species than trawlers; however, most of these constitute fishing resources in the study region. Of the
19 species whose maturation size is known, nine occurred in gillnets as juveniles, and of the 14
species for which the legal size of capture is established, seven occurred in gillnets in prohibited
sizes. Gillnets and trawlers presented size bycatch and affected different species between them, with
four resources that were present in bycatch from both gillnets and trawlers. The broad range of mesh
sizes employed by SSF warns of the discarding of undersized captures, and stresses the importance
of policies addressing gillnet management.
Key words: Artisanal fisheries, bycatch, fisheries management, Brazil.
Juveniles y peces pequeños en la pesca artesanal: las redes de enmalle no están menos impli-
cadas que la pesca de arrastre
RESUMEN. De particular preocupación en la pesca comercial es el tamaño de los organismos
en la captura incidental, es decir, la muerte de las primeras etapas de los recursos que alcanzarían
un valor comercial cuando se conviertan en adultos. Este evento se asocia frecuentemente con la
pesca de arrastre debido a la menor selectividad de tamaño de este arte en comparación con las redes
de enmalle. Sin embargo, esto es esperable cuando en las pesquerías de pequeña escala (PPE) se
emplean redes de enmalle simultáneamente en las redes de arrastre + redes de deriva que mezclan
varios tamaños de malla. Este trabajo analiza las capturas pesqueras y compara las características de
las capturas de peces en las redes de enmalle y en los arrastreros con respecto al tamaño de primera
madurez, el tamaño legal de la captura y los descartes esperados. Se obtuvieron datos de 2007-2021
para la PPE en el sur de Brasil. En los datos estuvieron representadas un total de 112 especies de
peces. Las redes de enmalle explotaron menos especies que los arrastreros; sin embargo, la mayoría
de estos constituyeron recursos pesqueros en la región de estudio. De las 19 especies cuyo tamaño
de maduración se conoce, nueve se encontraron en las redes de enmalle como juveniles, y de las 14
especies para las que se establece el tamaño legal de captura, siete se encontraron en redes de enma-
lle en tamaños prohibidos. Las redes de enmalle y los arrastreros presentaron captura incidental de
tamaño y afectaron a diferentes especies en forma conjunta, con cuatro recursos que estuvieron pre-
165
*Correspondence:
ptchaves@ufpr.br
Received: 10 August 2021
Accepted: 16 November 2021
ISSN 2683-7595 (print)
ISSN 2683-7951 (online)
https://ojs.inidep.edu.ar
Journal of the Instituto Nacional de
Investigación y Desarrollo Pesquero
(INIDEP)
This work is licensed under a Creative
Commons Attribution-
NonCommercial-ShareAlike 4.0
International License
Marine and
Fishery Sciences
MAFIS
ORIGINAL RESEARCH
Juveniles and undersized fish in small-scale fisheries: gillnets are not less
implied than trawling
PAULO DE TARSO DA CUNHA CHAVES*
Zoology Department, Federal University of Paraná, PO Box 19020, Code 81531-980 - Curitiba, Brazil.
ORCID Paulo de Tarso da Cunha Chaves https://orcid.org/0000-0001-6393-8256
INTRODUCTION
Small-scale fisheries (SSF) differ from large-
scale fisheries with respect to several technical,
economic, and social attributes. From a conserva-
tion perspective, fishing effort in SSF is often
more tolerable and catches are less focused on a
few stocks. By using passive gears such as hand
lines, fish traps, and gillnets, SSF tends to opti-
mize human work and reduce fuel consumption
(FAO 2016). These gears show higher capture
selectivity with respect to species and individual
size as compared to trawl nets (Armstrong et al.
1990; Wolff et al. 2015), another gear employed
by SSF fisheries as well as large-scale fisheries
(Misund et al. 2002; Santurtún et al. 2014). In
comparative studies between gillnets and trawl-
ing, Olin and Malinen (2003) found that in South
Finland fish smaller than 5 cm corresponded to
51% of trawler captures, while they corresponded
to only 1% of gillnet captures; and Huse et al.
(2000) found that the mean length of cod caught
in gillnets on the Norway coast was approximate-
ly 17 cm larger than those caught by trawl nets.
Trawling is known to generate bycatch (Silva-
Júnior et al. 2015; Cardoso et al. 2021). This pro-
motes design adaptations to reduce the capture
and consequent discarding of non-target species
and individuals (Alarcón Vélez et al. 2014;
Freiría et al. 2014), and strategies as in the
penaeid fisheries off Iran, where experiments are
being conducted to replace trawl nets with gill-
nets (Hout et al. 2021).
A particular concern regarding incidental cap-
tures is ‘size bycatch’, i.e., the death of juvenile
stages of fish, crustaceans, and cephalopods that
would reach a satisfactory price for selling as
adults. In Southern Brazil, size bycatch from
trawlers includes small individuals of marketable
species, such as Micropogonias furnieri (3% in
weight), Umbrina canosai (7%), and Cynoscion
guatucupa (14%) (Cardoso et al. 2021). Apart
from the economic loss, discarding resources that
are not targeted or are below the permitted cap-
ture size constitutes a sensitive problem because
of its ecological and ethical implications (San-
turtún et al. 2014).
Gillnets incidentally capture charismatic ani-
mals, such as turtles, birds, and mammals (Cheng
and Tien-Hsi 1997; Cardoso et al. 2011; FAO
2020). These captures do not produce discarding
of size bycatch origin (Santurtún et al. 2014),
probably because, as verified in the haddock and
the Arctic cod fisheries in Finland (Huse et al.
2000), rates of young-adults in catches are lower
with gillnets than with trawls and longlines.
However, gillnets also show size bycatch that
varies between mesh sizes, as observed in a fish
assemblage in a Brazilian lake (immature versus
mature individuals, Silvano et al. 2016), or with
depths of operation, as observed in the whiting
fisheries in the Black Sea (Kalayci and
Yeşilçiçek 2014).
Each mesh size is selective for a particular
morphology (Armstrong et al. 1990; Reis and
Pawson 1999). Gillnets mixing different meshes
are potentially efficient in capturing a larger spec-
trum of fish morphologies, widening the range of
vulnerable sizes for capture. The use of setnets
and driftnets is common in SSF, particularly in
tropical waters, where many target resources
share a common area (Alves et al. 2012; Wolff et
al. 2015). The present work investigates how the
employment of multiple mesh sizes in a restricted
166 MARINE AND FISHERY SCIENCES 35 (2): 165-180 (2022)
sentes en la captura incidental tanto de redes de enmalle como de arrastreros. La amplia gama de tamaños de malla empleados por la
PPE es una advertencia sobre el descarte de capturas de tamaño pequeño y enfatiza la importancia de políticas que aborden el manejo
de las redes de enmalle.
Palabras clave: Pesquería artesanal, captura incidental, manejo pesquero, Brasil.
area results in higher size diversity in the catch,
comparatively to trawling. If such heterogeneity
includes fish with no marketable value or prohib-
ited species and size classes, they are discarded
on board or after landing. Is it plausible to sup-
pose that, in such conditions, gillnets capture
juveniles and undersized fish at a not-smaller
scale than trawl, and are also harmful for fisheries
sustainability?
Along the littoral coast of Southern Brazil, in
shallow waters up to 30 m, gillnets and trawl nets
are the main fishing gears employed by SSF
(Chaves and Robert 2003). Gillnets are deployed
from the bottom to the surface and target several
teleosts and chondrichthyan species. Trawling is
performed on the bottom and targets shrimp.
Both gears register incidental captures, mainly
fish and invertebrates. While the small meshes
used for trawling (1-2 cm) catch an important
abundance of benthic fauna, including small fish
(Pina and Chaves 2009; Chaves and Silva 2019),
the larger meshes used for gillnets (5-20 cm)
retain a considerable number of non-target fish
(Chaves et al. 2019; Afonso and Chaves 2021).
This study analyzes the fish size in trawling and
gillnets captures, comparing the two gears with
respect to three parameters: legal size of capture,
size at first maturation, and expected discards.
Does trawling affect more undersized (legal cap-
ture and/or first maturation) species than gill-
nets? With respect to legal capture and first mat-
uration, what is the species performance of each
gear? What target resources occur as bycatch in
these gears?
MATERIALS AND METHODS
The study area is located in Southern Brazil,
on the coasts of Parana and Santa Catarina states,
25° 30'S-26° 10'S; 48° 10'S-48° 40'W. This
corresponds to the fishing area of three SSF com-
munities: Matinhos, Itapoa, and São Francisco
do Sul (Figure 1). The fishing fleet consists of
between 30 and 50 fiberglass canoes in each
167
CHAVES: JUVENILES AND UNDERSIZED FISH CAUGHT BY GILLNETS
Figure 1. Study area (small square) on Southern Brazilian coast and location of fishing communities of Matinhos, Itapoa, and
São Francisco do Sul (arrows).
Brazil
Curitiba
Florianopolis
Matinhos
Itapoa
São Francisco de Sul
Southwestern Atlantic
Ocean
49° W 48° W
26° S 25'S
community, measuring 8-12 m, all motorized
with < 60 HP. They are equipped with a gillnet
and/or with bottom trawling gear. Fishers per-
form one-day trip, but gillnets fish for up to six
days continuously. In trawling, two nets are
simultaneously pulled by canoes at depths of 8-
15 m in successive hauls during 6-8 h per day.
The mesh size at the codend is 1-2 cm between
opposite knots, and the target resource is the
seabob shrimp Xiphopenaeus kroyeri. Gillnets
have a height of up to 20 m and a length of a few
hundred to four thousand meters. They are fixed
to the bottom or drifting at depths of 10-30 m.
Mesh sizes are diverse, typically 5, 7, 9, 11, 12,
and 20 cm between opposite knots, depending on
the target resource, sharks and teleosts. The latter
primarily belong to Mugilidae, Scombridae,
Pomatomidae, Sciaenidae, and Pleuronecti-
formes. Technical specifications of trawl nets
and gillnets used in the study area, target
resources, and modes of operation are described
by Chaves and Robert (2003), Nogueira et al.
(2011), Chaves et al. (2019), and Afonso and
Chaves (2021).
The range of total length (TL) by species and
the minimum and maximum TL values were
linked with gillnets or shrimp trawling. The
sources used were: (i) previous works carried out
in the study area from 2007-2016; fish were
obtained by monitoring landings in the cited com-
munities, or experimental cruises for academic
research using boats and fishing gears routinely
employed by them; and (ii) original data obtained
by monitoring landings of the Matinhos fleet dur-
ing 2020-2021. In experimental cruises, all indi-
viduals were measured, while in monitored land-
ings individuals were accessed by chance.
Because most of the sources did not discriminate
between the mesh size of gillnets, they were con-
sidered as a single entity.
For each species, the largest TL landed by
trawlers (Max. TL T) and/or the smallest TL land-
ed by gillnetters (Min. TL G) were identified.
These data were compared with two other specif-
ic TL values: the minimum size of legal capture
(TL C), and the average size at first maturation
(TL50), preferentially in this area or, when not
available, in Brazil. When TL50 differed between
sexes, the largest value was adopted. Values of
TL C came from federal rules MMA 53/05
(MMA 2005) and IBAMA 83/06 (MMA 2006),
while those of TL50 came from the literature.
Species of commercial interest in the study
area were recognized after the findings of Chaves
and Robert (2003), Chaves et al. (2019), and
Afonso and Chaves (2021), and designated as
fishing resources. Carcharhinus sp., Diplectrum
sp., Paralichthys sp., and Sphyrna sp. refer to two
or more species occurring in the study area and
are not always recognized at species level. To
simplify the representation of results, each genus
was considered a single species.
RESULTS
Values of Max. TL T were compiled from 100
species and those of Min. TL G from 32 species.
Overall, data on 112 species were compiled with
more than 30% (42) constituting fishing
resources in the study area (Table 1).
The number and weight of catches were not
quantified, but data indicate that, all species con-
sidered, individuals < 100 mm were vulnerable
almost exclusively to trawling, while those in the
range of 100-300 mm were vulnerable to both
trawling and gillnets. A few species were repre-
sented in trawl nets by individuals > 500 mm or
occur in gillnets with individuals not smaller than
500 mm (Figure 2). Gears partially shared the
ranges 36-940 mm for Max. TL T, and 110-720
mm for Min. TL G (Table 1). Most representative
size classes corresponding to > 10% of frequency
of occurrence confirmed significant captures by
both gears of species within TLs 100-300 mm:
Max. TL T at classes 110-230 mm, and Min. TL
G at classes 110-270 mm (Figure 2).
168 MARINE AND FISHERY SCIENCES 35 (2): 165-180 (2022)
169
CHAVES: JUVENILES AND UNDERSIZED FISH CAUGHT BY GILLNETS
Table 1. Fish species caught by small-scale fisheries in Parana and Santa Catarina littoral, Southern Brazil. Part of them (*) constitute fishing resources in
this area. Max. TL T, Min. TL G: maximum and minimum total length (TL) in trawling or gillnets, respectively. TL C: minimum TL of legal capture.
TL50: average TL at first maturation. Ref.: references see below. Code applies to species of Figure 6.
Max. TL Ref. Min. TL Ref. TL C Ref. TL50 Ref. Code
T (mm) G (mm) (mm) (mm)
Achirus declivis Chabanaud, 1940 190 1, 2, 3
Achirus lineatus (Linnaeus, 1758) 112 1
Anchoa januaria (Steindachner, 1879) 139 1 65 17 ANJA
Anchoa lyolepis (Evermann and Marsh, 1980) 87 3
Anchoa spinifera Valenciennes, 1840 177 1, 3
Anchoa tricolor Spix and Agassiz, 1829 113 1, 3
Anchovia clupeoides (Swaison, 1839) 156 3
Anchoviella brevirostris (Günther, 1868) 136 3
Anchoviella lepidentostole (Fowler, 1911) 119 2 94 17 ANLE
Anisotremus surinamensis (Bloch, 1791) 277 2
Aluterus monoceros (Linnaeus, 1758) 477 1
Aspistor luniscutis (Valenciennes, 1840) 256 2
Astroscopus y-graecum (Cuvier, 1829) 65 3
Bairdiella ronchus (Cuvier, 1830) 180 1, 2, 3 158 17 BARO
Carcharhinus sp.* 455 7 1,150
Cathorops spixii (Agassiz, 1829)* 273 1, 3
Centropomus parallelus Poey, 1860* 347 2, 3 210 8 300 10 200 11 CEPA
Centropomus undecimalis Bloch, 1792* 267 2, 3 500 10
Cetengraulis edentulus (Cuvier, 1829) 131 2 137 17 CEED
Chaetodipterus faber (Broussonet, 1782) 114 1, 3 305 7
Chilomycterus spinosus (Linnaeus, 1758) 80 1, 3
Chirocentrodon bleekerianus (Poey, 1867) 141 1, 3 76 17 CHBL
Chloroscombrus chrysurus (Linnaeus, 1766)* 159 1, 2, 3 200 7 120 10 124 17 CHCH
Citharichthys arenaceus Evermann and Marsh, 1900 186 1, 3
Citharichthys spilopterus Günther, 1862 173 1, 2, 3
Conodon nobilis (Linnaeus, 1758) 193 1, 2, 3
Ctenosciaena gracilicirrhus (Metzelaar, 1919) 148 2, 3
Cynoscion acoupa (Lacepède, 1801)* 300 8 427 17 CYAC
170 MARINE AND FISHERY SCIENCES 35 (2): 165-180 (2022)
Table 1. Continued.
Max. TL Ref. Min. TL Ref. TL C Ref. TL50 Ref. Code
T (mm) G (mm) (mm) (mm)
Cynoscion guatucupa (Cuvier, 1830)* 240 8 346 17 CYGU
Cynoscion leiarchus (Cuvier, 1830)* 200 7, 8
Cynoscion virescens (Cuvier, 1830)* 142 2
Dactylopterus volitans (Linnaeus, 1758) 230 1, 3
Dactylopterus auratus Ranzani, 1842* 171 3
Diapterus rhombeus (Cuvier, 1829)* 197 1, 2, 3 150 13 DIRH
Diplectrum radiale (Quoy and Gaimard, 1824) 184 1, 3
Diplectrum sp. (D. radiale or D. formosum) 190 8
Engraulis anchoita Hubbs and Marini, 1835 108 1
Etropus crossotus Jordan and Gilbert, 1822 174 1, 3 85 17 ETCR
Eucinostomus gula (Cuvier, 1830)* 180 3 150 13 110 17 EUGU
Eucinostomus. melanopterus (Bleeker, 1863)* 234 1, 3
Eugerres brasilianus (Cuvier, 1830)* 263 2 200 8 170 150 17 EUBR
Genidens barbus (Lacepède, 1830)* 171 1 410 7 400 10 415 17 GEBA
Genidens genidens (Cuvier, 1829)* 194 1 118 17 GEGE
Gempylus serpens Cuvier, 1829 106 1
Gobiesox barbatulus Starks, 1913 53 3
Gymnothorax ocellatus Agassiz, 1834 495 1, 3
Harengula clupeola (Cuvier, 1829) 166 2, 3
Hemicaranx amblyrhynchus (Cuvier, 1833) 210 2, 3
Isopisthus parvipinnis (Cuvier, 1830) * 194 1, 2, 3 180 8 159 12 ISPA
Lagocephalus laevigatus (Linnaeus, 1766) 173 2, 3
Larimus breviceps Cuvier, 1830* 256 1, 2 110 8 135 14 LABR
Lycengraulis grossidens (Agassiz, 1829) 150 1, 3
Macrodon ancylodon (Bloch and Schneider, 1891)* 224 1, 3 190 7, 8 250 10 237 17 MAAN
Menticirrhus americanus (Linnaeus, 1758)* 261 1, 2, 3, 4 177 17 MEAM
Menticirrhus littoralis (Holbrook, 1860)* 229 1 200 10 230 15 MELI
Micropogonias furnieri (Desmarest, 1823)* 274 1, 2, 3 190 7, 8 250 10 306 17 MIFU
Mugil liza Valenciennes, 1836* 450 7, 8 350 10 350 17 MULI
Myrophis punctatus Lütken, 1852 510 3
171
CHAVES: JUVENILES AND UNDERSIZED FISH CAUGHT BY GILLNETS
Table 1. Continued.
Max. TL Ref. Min. TL Ref. TL C Ref. TL50 Ref. Code
T (mm) G (mm) (mm) (mm)
Narcine brasiliensis (Olfers, 1831) 202 1, 2 288 17 NABR
Nebris microps Cuvier, 1830 331 1, 2 270 8
Ophichthus gomesii (Castelnau, 1855) 595 1, 3
Ophichthus parilis (Richardson, 1848) 471 3
Oligoplites saliens (Bloch, 1793) 270 7, 8
Oligoplites saurus (Bloch and Schneider, 1801) 213 1
Ophidium holbrooki (Putnam, 1874) 225 1, 3
Ophioscion punctatissimus 155 1, 3
Meek and Hildebrand, 1925
Opisthonema oglinum (Lesueur, 1817)* 185 1, 3 208 8 150 10 115 17 OPOG
Orthopristis ruber (Cuvier, 1830) 275 1, 2, 3 156 17 ORRU
Paralichthys sp. (P. brasiliensis or P. patagonicus)* 300 7 350 10
Paralonchurus brasiliensis (Steindachner, 1875)* 250 1, 2, 3, 5 160 8 149 14 PABR
Pellona harroweri (Fowler, 1917) 246 1, 2, 3
Peprilus paru (Linnaeus, 1758)* 185 1, 3 200 8 150 10 120 17 PEPA
Peprilus xanthurus (Quoy and Gaimard, 1825)* 210 7
Platanichthys platana (Regan, 1917) 124 3
Polydactylus oligodon (Günther, 1860) 214 1
Polydactylus virginicus (Linnaeus, 1758) 190 2, 3
Pomadasys corvinaeformis (Steindachner, 1868)* 214 1, 2, 3 175 8
Porichthys porosissimus (Cuvier, 1829) 265 1, 3
Priacanthus arenatus Cuvier, 1829 270 7
Prionotus punctatus (Bloch, 1797)* 272 1, 3 180 7 180 10 262 17 PRPU
Prionotus nudigula Ginsburg, 1950* 111 2
Pseudobatos percellens (Walbaum, 1792) 645 1, 2 430 7 583 17 PSPE
Rypticus randalli Courtenay, 1967 176 1, 3
Sardinella janeiro (Eigenmann, 1894) 149 3 192 17 SAJA
Scomberomorus brasiliensis 206 1 210 7, 9 370 446 9 SCBR
Collette, Russo and Zavala-Camin, 1978*
Selene setapinnis (Mitchill, 1815) * 195 1, 3 205 17 SESE
172 MARINE AND FISHERY SCIENCES 35 (2): 165-180 (2022)
Table 1. Continued.
Max. TL Ref. Min. TL Ref. TL C Ref. TL50 Ref. Code
T (mm) G (mm) (mm) (mm)
Selene vomer (Linnaeus, 1758) * 110 1, 3 305 7,8
Serranus phoebe Poey, 1851 112 1
Sphoeroides greeleyi (Gilbert, 1900) 124 1, 3 70 17 SPGR
Sphoeroides testudineus (Linnaeus, 1758) 260 1, 3 108 17 SPTE
Sphyraena guachancho Cuvier, 1829 331 3
Sphyrna sp. (S. lewini or S. zygaena)* 720 7 600 10
Stellifer brasiliensis (Schultz, 1945)* 190 1, 2, 3 73 17 STBR
Stellifer rastrifer (Jordan, 1889)* 215 1, 2, 3 98 17 STRA
Stellifer sp. (species not described)* 124 1, 2, 3
Stellifer stellifer (Bloch, 1790)* 175 1, 2, 3 75 17 STST
Stephanolepis hispidus (Linnaeus, 1766) 202 3 139 17 STHI
Syacium micrurum Ranzani, 1842 175 3
Syacium papillosum (Linnaeus, 1758) 239 3
Symphurus jenynsi (Evermann, 1906) 158 3
Symphurus plagusia (Bloch and Schneider, 1801) 168 2
Symphurus tessellatus (Quoy and Gaimard, 1824) 200 1, 2, 3
Syngnathus folletti Herald, 1942 130 2
Synodus foetens (Linnaeus, 1766) 224 3
Thalassophryne nattereri Steindachner, 1876 36 1
Trichiurus lepturus Linnaeus, 1758* 940 1, 2, 3, 6 550 7, 8 700 10 506 17 TRLE
Trinectes microphthalmus (Chabanaud, 1928) 165 2, 3
Trinectes paulistanus (Ribeiro, 1915) 165 1, 3
Umbrina coroides Cuvier, 1830* 200 3
Urophycis brasiliensis (Kaup, 1858)* 265 1, 2, 3
Zapteryx brevirostris (Müller and Henle, 1841) 551 1, 2 380 7 506 16 ZABR
Ref.: 1: Pina and Chaves (2009); 2: Pinheiro (2016); 3: Souza and Chaves (2007); 4: Muniz and Chaves (2008); 5: Robert et al. (2007); 6: Del Puente and
Chaves (2009); 7: Afonso and Chaves (2021); 8: original data; 9: Chaves et al. (2021); 10: MMA (2005); 11: Chaves and Nogueira (2018); 12: Romero et
al. (2008); 13: MMA (2006); 14: Silva-Júnior et al. (2015); 15: Braun and Fontoura (2004); 16: Colonello and Menni (2011); 17: Froese and Pauly (2021).
Twenty species were common to both gears,
and 70% of them had Max. TL T > Min. TL G
(Figure 3). Species represented in trawling by
individuals < 200 mm only contained Min. TL G
> Max. TL T. Conversely, individuals > 200 mm
presented TL T > Min. TL G (Figure 3).
Among the 20 species common to trawling and
gillnets, 16 constitute fishing resources in the
study area (Figure 4). Thirteen species, ten of
which are fishing resources in the region, present-
ed the relationship ‘Max. TL T/Min. TL G’ > 1.0.
This reveals that trawling also acts on important
sizes that are larger than the smallest individuals
caught by gillnets. For five resources, Prionotus
punctatus, Paralonchurus brasiliensis, Centropo-
mus parallelus, Trichiurus lepturus, and Larimus
breviceps, trawling catches individuals up to 1.5-
2.3 times larger than the smallest ones caught by
gillnets (Figure 4). The other 26 fishing resources
were classified under trawling (18) or gillnets (8)
(Table 1).
The minimum size of legal capture (TL C) was
established for 18 fishing resources (Table 1).
Trawling exploits 13 of these species. Nearly
70% (9) presented the relationship ‘Max. TL
T/TL C’ > 1; however, it is expected that all 13
species have individuals caught with TL < TL C.
Gillnets exploited 14 resources; half of them pre-
sented the relationship ‘Min. TL G/TL C’ > 1, and
prohibited sizes were probably not caught by gill-
nets. The other 50% (seven resources) presented
Min. TL G < TL C and were vulnerable to being
captured at prohibited sizes (Figure 5).
The average size at first maturation is known
for 40 species (Table 1). Trawling exploited 37 of
them. Nearly 75% (29) presented the relationship
‘Max. TL T/TL50 > 1; however, it is expected
that all 37 species caught individuals with TL <
TL50. Gillnets exploited 19 species. Nearly 55%
of them presented the relationship ‘Min TL
G/TL50 > 1, and probably are not caught by gill-
nets before the first maturation. Conversely, 45%
(9 species) presented Min TL G < TL50 and were
vulnerable to gillnets as juveniles (Figure 6).
For trawling, nearly 75% (19/25) of fishing
resources analyzed for maturation size presented
the relationship ‘Max. TL T/TL50 > 1, but it is
expected that all 25 resources caught individuals
173
CHAVES: JUVENILES AND UNDERSIZED FISH CAUGHT BY GILLNETS
Figure 2. Relative frequencies of species (N = 112) according to individual total length (TL) registered in small-scale fisheries
in Southern Brazil grouped in 40 mm size classes. Maximum TL in trawling: wide line, 100 species; minimum TL in
gillnets: narrow line, 32 species.
0
5
10
15
20
25
30
35
30 70 110 150 190 230 270 310 350 390 430 470 510 550 590 630670 710 750 790 830 870 910
TL (mm)
Relative frequency (%)
174 MARINE AND FISHERY SCIENCES 35 (2): 165-180 (2022)
Figure 4. Species of common occurrence in both fishing gears (trawl nets and gillnets) in Southern Brazilian small-scale fish-
eries, and values of the relationship between the maximum total length in trawling (Max. TL T) and the minimum TL in
gillnets (Min. TL G). *: species that constitute fishing resources in the study area.
0
1
2
3
Max. TL T/Min. TL G
Species
Selene vomer*
Chaetodipterus faber
Genidens barbus*
Chloroscombrus chrysurus*
Opisthonema oglinum*
Peprilus paru*
Stellifer brasiliensis*
Isopisthus parvipinnis*
Macrodon ancylodon*
Pomadasys corvinaeformis*
Nebris microps
Eugerres brasilianus*
Micropogonias furnieri*
Zapteryx brevirostris
Pseudobatos percellens
Prionotus punctatus*
Paralonchurus brasiliensis*
Centropomus parallelus*
Trichiurus lepturus*
Larimus breviceps*
Figure 3. Distribution of values of maximum total length (TL) in trawling (dark circles) and/or of minimum total length in gill-
nets (white circles) of 112 species caught by small-scale fisheries in Southern Brazil.
0
100
200
300
400
500
600
700
800
900
1,000
0112
Species
TL (mm)
with TL < TL50. For gillnets, nearly 60% (10/17)
of the resources presented ‘Min TL G/TL50 ≥ 1,
and probably were not caught before the first
maturation. However, 40% (7 resources) present-
ed Min TL G < TL50 and were vulnerable to gill-
nets in juvenile conditions (Figure 6).
175
CHAVES: JUVENILES AND UNDERSIZED FISH CAUGHT BY GILLNETS
Figure 6. Relationship between total length (TL) in catches and average TL of maturation (TL50) in species exploited by small-
scale fisheries in Southern Brazil. Dark circles indicate the maximum TL in trawling; white circles indicate the minimum
TL in gillnets. *: species that constitute fishing resources in the study area. Species code: Table 1.
Figure 5. Relationship between total length (TL) in catches and TL of legal capture in resources exploited by small-scale fish-
eries in Southern Brazil. Dark circles indicate the maximum TL in trawling; white circles indicate the minimum TL in
gillnets.
0
1
2
TL catches/legal capture
Resources
Genidens barbus
Centropomus undecimalis
Stellifer brasiliensis
Menticirrhus americanus
Micropogonias furnieri
Menticirrhus littoralis
Centropomus parallelus
Eucinostomus gula
Opisthonema oglinum
Chloroscombrus chrysurus
Trichiurus lepturus
Prionotus punctatus
Eugerres brasilianus
Carcharhinus sp.
Paralichthys sp.
Sphyrna sp.
Mugil liza
0
1
2
3
TL catches/TL
50
Species code
Fishing resources caught of undersized for
legal capture and/or before the first maturation
constitute incidental capture in such gear. In
trawling, size bycatch affects Genidens barbus,
Centropomus undecimalis, Scomberomorus
brasiliensis, Menticirrhus americanus, M. lit-
toralis, M. furnieri, and Selene setapinnis; in gill-
nets, S. brasiliensis M. americanus, M. furnieri,
Centropomus parallelus,Trichirus lepturus,Car-
charhinus sp., Paralichthys sp., Prionotus punc-
tatus, Larimus breviceps,Cynoscion guatucupa,
and C. acoupa are affected (Figures 5 and 6).
DISCUSSION
Data showed that trawlers catch thrice the
number of species than gillnetters, which reflects
different selectivity between the two gears (Arm-
strong et al. 1990; Alarcón Vélez et al. 2014), as
well as the mode and depth of operation. Active
fishing, which is independent of fish movements
and explores shallow waters, are the advantages
of shrimp trawling, which result in higher yields
than gillnets, which frequently work at the bottom
up to 30 m depth (Chaves and Robert 2003; Afon-
so and Chaves 2021). Previous studies have
pointed out a bathymetric heterogeneity in fish
size distribution, with smaller individuals occupy-
ing mostly shallower waters, while larger ones
occupy deeper waters. A similar trend was report-
ed by Macpherson and Duarte (1991), who
referred to demersal fish in the SE Atlantic (44
species) and the NW Mediterranean (31 species).
This was also observed in the pelagic tuna fishery
in Asia (FAO 2016). The size-depth relationship
associated with gear selectivity helps to explain
the size differences between captures from the
gears, the smallest TL of 36 mm was found for
trawling, and 100 mm for gillnets. Even so, the
range of minimum TL of species caught by gill-
nets reached 610 mm, which is an important value
in view of their high selectivity. This is due to the
multiple mesh sizes found in setnets plus drift-
nets, from 5 to 20 cm between opposite knots,
exceptionally up to 45 cm, operating simultane-
ously and/or alternately along the year (Chaves
and Robert 2003; Afonso and Chaves 2021).
The minimum size of legal capture (TL C) is
normally determined based on the reproductive
condition, for example, the smallest mature fish,
the average size of maturation (TL50), or the size at
which 100% of fish are mature (Sunil Mohamed et
al. 2014). When TL C is larger than TL50, it
denotes caution in fisheries management. In the
present work, TL50 was estimated for some
species, and TL C was established for a lower
number of resources. The values of these parame-
ters are derived from various regions on the Brazil-
ian coast, and in certain species both TL C and
TL50 refer to two different stocks. Although not
definitive, results indicate undersized individuals
in bycatch that also occur in gillnets in the study
area. The size at first maturation exceeded the
maximum size caught by trawling in eight species,
as well as the minimum size caught by gillnets in
nine species. This means that undersized fish are
caught by trawling (as expected) as well as by gill-
nets. Both conditions simultaneously apply to four
species: G. barbus,S. brasiliensis, M. furnieri, and
Macrodon ancylodon. These species play an
important role in landings in Southern Brazil
(MMA 2005; Chaves and Silva 2019; Chaves et al.
2021), and juveniles are being exploited by both
trawling and gillnets. Because more species are
caught by trawling, this gear acts on more under-
sized species than gillnets. However, relative to
the number of species occurring in each gear, the
size bycatch from gillnets is significant.
Capture of resources smaller than TL50 by gill-
nets in Brazilian waters has long been reported.
Alves et al. (2012) studied mesh sizes of 7-13 cm
and found undersized individuals in five of six
species, including S. brasiliensis and M. furnieri.
The status of the other three species recognized in
the present work as occurring in gillnets is
unknown because of the lack of data on TL C or
176 MARINE AND FISHERY SCIENCES 35 (2): 165-180 (2022)
TL50. Indeed, there are resources (e.g., Centropo-
mus undecimalis and Menticirrhus littoralis) that
also occur in gillnets (Afonso and Chaves 2021),
but were not presented here because data on Min.
TL G were not available.
The number and biomass in captures were not
considered, nor were the discards accomplished on
board in the case of commercial samplings. It is
expected that in a single haul of trawling, a signif-
icant number of small fish were caught than with a
similar effort using gillnets. On the other hand,
considering the large area used to deploy gillnets
(thousands of meters), and their period of exposure
(up to six days fulltime), the total fishing effort of
gillnets is intense, and the impact of gillnets on
juveniles and undersized fish is not negligible. In
the study area, SSF is only managed with respect to
trawling; there are no policies on gillnet effort with
respect to extension, time of exposure, or manage-
ment by quotas. Only a few resources are subject to
local rules disposing on the non-capture of young
or of adults in the spawning period (Chaves and
Silva 2019), and on the capture of threatened elas-
mobranchs (Chaves et al. 2019). In view of the
occurrence of threatened teleost species in the
study area, Afonso and Chaves (2021) recom-
mended an effort reduction of gillnet with a mesh
size of 18 cm at the end of winter and spring. San-
turtún et al. (2014) stated that, for stocks that are
not managed by quota, the biggest problem was
discards due to minimum landing size, an alert that
highlights the relevance of the present findings
with respect to size bycatch in gillnets.
In the present work, gillnet captures were not
individualized by mesh size, an omission that pre-
vents an accurate analysis of the gear types most
implied in non-target captures. Measures to
reduce the capture of undersized fish, proposed
by Alarcón Vélez et al. (2014), include the
turnover of fishing areas and the extension of
close seasons for fishing, taking into account the
presence of juveniles. Alves et al. (2012) added
that gillnet management should consider the ear-
lier period of the reproductive cycle, since ovari-
an development increases the fish perimeter at the
first dorsal fin in M. furnieri and other teleosts.
The influence of the reproductive cycle on mesh
size selectivity, first described by McCombie and
Berst (1969), affects adult fish, but is usually
ignored in fishery rules.
This work highlights the suggestion of Car-
doso et al. (2021) with respect to catches, and the
partial discarding of fish that could be caught in
bigger sizes and provides higher yields. It applies
not only to fish and shrimp trawlings, but also to
gillnets. Furthermore, from a global conservation
perspective, gillnets affect vertebrates such as
sharks, turtles, mammals, and penguins and other
birds, when migrating in waters exposed to set-
nets and driftnets (Cheng and Tien-Hsi 1997;
FAO 2020), presenting a strong challenge for
monitoring and control. Following Santurtún et
al. (2014), in view of the size bycatch existing in
both trawling and gillnets, it is recommended to
implement landing obligations for all catches,
except for species with a high survival rate after
release. According to these authors, time can be
provided to fishers’ organizations to develop
innovative solutions to trade these undersized
fish, or to find processed products that use the
otherwise discarded fish as raw material.
ACKNOWLEDGMENTS
Author is grateful to three anonymous referees,
and to the MAFIS Editor, by the time they have
consecrated to the manuscript, and to the Matin-
hos fishers, by their assistance for data collection.
REFERENCES
AFONSO MG, CHAVES PT. 2021. A pesca de emal-
he costeiro de pequena escala no litoral do
Paraná: um estudo de caso para a conservação.
177
CHAVES: JUVENILES AND UNDERSIZED FISH CAUGHT BY GILLNETS
Rev CEPSUL Biodiv Cons Mar. 10:
e2021001. doi:10.37002/revistacepsul.v10.
1754e2021001
ALARCÓN VÉLEZ JR, SALAZAR CÉSPEDES CM,
GUEVARA CARRASCO R, AUBONE A, CHACÓN
G, CORNEJO R, GARCIA JC, HANOZA F, et al.
2014. Experiencias de selectividad con red de
arrastre de fondo utilizando grillas de selec-
ción aplicado a la merluza peruana (Merluc-
cius gayi peruanus). Rev Invest Desarr Pesq.
25: 83-95.
ALVES PMF, ARFELLI CA. TOMÁS ARG. 2012.
Selectivity of bottom gillnet of Southeastern
Brazil. Bol Inst Pesca. 38 (4): 275-284.
ARMSTRONG DW, FERRO RST, MACLENNAN DN,
REEVES AS. 1990. Gear selectivity and the
conservation of fish. J Fish Biol. 37 (A): 261-
262.
BRAUN AS, FONTOURA NF. 2004. Reproductive
biology of Menticirrhus littoralis in Southern
Brazil (Actinopterygii: Perciformes: Sci-
aenidae). Neotrop Ichthyol. 2: 31-36. doi:10.
1590/S1679-62252004000100005
CARDOSO LG, BUGONI L, MANCINI L, HAIMOVICI
M. 2011. Gillnet fisheries as a major mortality
factor of Magellanic penguins in wintering
areas. Mar Pollut Bull. 62: 840-844.
doi:10.1016/j.marpolbul.2011.01.033
CARDOSO LG, MONTEIRO DS, HAIMOVICI M.
2021. An assessment of discarded catches
from the bottom pair trawling fisheryin sou-
thern Brazil. Mar Fish Sci. 34 (2): 197-210.
doi:10.47193/mafis.3422021010609
CHAVES PTC, ALMEIDA MP, PLATNER M. 2019.
Tubarões e raias como captura incidental na
pesca artesanal do litoral do Paraná: condição
reprodutiva e variações sazonais em composi-
ção e abundância. Arq Cien Mar. 52: 7-23.
CHAVES PTC, NOGUEIRA AB. 2018. Biologia
reprodutiva do robalo-peva, Centropomus
parallelus (Teleostei), na Baía de Guaratuba
(Brasil). Acta Biol Paran. 47: 69-84.
CHAVES P, ROBERT MC. 2003. Embarcações, artes
e procedimentos da pesca artesanal no litoral
sul do Estado do Paraná, Brasil. Atlantica. 25:
53-59.
CHAVES PT, SILVA AVF. 2019. Recursos-alvo que
são também bycatch, e recomendação para a
gestão da pesca de emalhe no litoral do Para-
ná, Brasil. Rev CEPSUL Biodiv Cons Mar. 8:
1-11. https://doi.org/10.37002/revistacepsul.
vol8.732e2019001
CHAVES PTC, VAZ-DOS-SANTOS AM, BIRNFELD
PO. 2021. Population dynamics of Scombero-
morus brasiliensis from a small-scale fishery
of the Southwestern Atlantic Ocean. Ocean
Coast Res. 69: 1-17. doi:10.1590/2675-
2824069.20-016pdtdcc
CHENG JJ, TIEN-HSI C. 1997. The incidental cap-
ture of five species of sea turtles by coastal
setnet fisheries in the eastern waters of Tai-
wan. Biol Conserv. 82: 235-239.
COLONELLO JC, MENNI RC. 2011. Reproductive
biology of the lesser guitarfish Zapteryx brevi-
rostris from the south-western Atlantic Ocean.
J Fish Biol. 78: 287-302. doi: 10.1111/j.1095-
8649.2010.02864.x
DEL PUENTE SV, CHAVES P. 2009. Atividade
reprodutiva do peixe-espada, Trichiurus leptu-
rus (Teleostei), vulnerável à pesca de pequena
escala no extremo-norte do litoral de Santa
Catarina, Brasil. Biotemas. 22: 77-84.
[FAO] FOOD AND AGRICULTURE ORGANIZATION OF
THE UNITED NATIONS. 2016. Technical and
socio-economic characteristics of small-scale
coastal fishing communities, and opportuni-
ties for poverty alleviation and empowerment,
by Uwe Tietze. FAO Fisheries and Aquacul-
ture Circular. 1111. 136 p.
[FAO] FOOD AND AGRICULTURE ORGANIZATION OF
THE UNITED NATIONS. 2020. Report of the
expert meeting to develop technical guidelines
to reduce bycatch of marine mammals in cap-
ture fisheries. Rome, Italy, 17-19 September
2019. FAO Fisheries and Aquaculture Report.
1289. 85 p. doi:10.4060/ca7620en
FREIRÍA J, CHOCCA JG, MARIN Y, G ONZALEZ B,
BEATHYATE G. 2014. Diseño y ensayo de redes
178 MARINE AND FISHERY SCIENCES 35 (2): 165-180 (2022)
de arrastre de fondo orientadas al escape de
juveniles. Rev Invest Desarr Pesq. 25: 59-73.
FROESE R, PAULY D. Editors. 2021. FishBase.
https://www.fishbase.org.
HOUT A, PAIGHAMBARI SY, EIGHANI M, BROAD-
HURST MK, BAYSE SM. 2021. Utility of gill-
nets for selectively targeting penaeids off Iran.
Aquaculture and Fisheries. doi:10.1016/j.aaf.
2021.02.002
HUSE I, LØKKEBORG S, SOLDAL AV. 2000. Rela-
tive selectivity in trawl, longline and gillnet
fisheries for cod and haddock. ICES J Mar
Sci. 57: 1271-1282. doi:10.1006/jmsc.2000.
00813
KALAYCI F, YEŞILÇIÇEK T. 2014. Effects of depth,
season and mesh size on the catch and dis-
cards of whiting (Merlangius merlangus euxi-
nus) gillnet fishery in the Southern Black Sea,
Turkey. Turk J Fish Aquat Sci. 14: 449-456.
doi:10.4194/1303-2712-v14_2_15
MACPHERSON E, DUARTE CM. 1991. Bathymetric
trends in demersal fish size: is there a general
relationship? Mar Ecol Prog Ser. 71: 103-112.
MCCOMBIE AM, BERST AH. 1969. Some effects
of shape and structure of fish on selectivity of
gillnets. J. Fish Res Board Can. 26 (10): 2681-
2689. doi:10.1139/f69-260
MISUND OA, KOLDING J, FRÉON P. 2002. Fish
capture devices in industrial and artisanal fish-
eries and their influence on management. In:
HART PJV, REYNOLDS JD, Editors. Handbook
of fish biology and fisheries. Vol. 2. Fisheries.
Malden: Blackwell Publishing, p. 13-36.
doi:org/10.1002/9780470693919.ch2
MMA 2005. Instrução Normativa MMA, de 22
de novembro de 2005. Estabelece o tamanho
mínimo de captura de espécies marinhas e
estuarinas do litoral sudeste e sul do Brasil.
Diário Oficial da União, Brazil, 24/Novem-
ber/2005.
MMA 2006. Instrução Normativa IBAMA, de 5
de janeiro de 2006. Proíbe, no Município de
Canavieiras, no Estado da Bahia, a captura, o
desembarque, o transporte, o armazenamento,
o beneficiamento e a comercialização das
espécies que especifica. Diário Oficial da
União, Brazil, 05/January/2006.
MUNIZ E, CHAVES PT. 2008. Condição reproduti-
va da betara preta, Menticirrhus americanus
(Teleostei, Sciaenidae), na pesca realizada no
litoral norte de Santa Catarina, Brasil. Acta Sci
Biol Sci. 30 (4): 339-344. doi:10.4025/actasci-
biolsci.v30i4.1230
NOGUEIRA AB, CHAVES PT, ROBERT MC, AGUIAR
KD. 2011. Participação da fisiografia local na
composição dos atributos e estratégias de pesca
no sul do Brasil. Bol Inst Pesca. 37: 13-30.
OLIN M, MALINEN T. 2003. Comparison of gillnet
and trawl in diurnal fish community sampling.
Hydrobiologia. 506-509: 443-449.
PINA JV, CHAVES P. 2009. Incidência da pesca de
arrasto camaroeira sobre peixes em atividade
reprodutiva: uma avaliação no litoral norte de
Santa Catarina, Brasil. Atlantica. 31: 99-106.
PINHEIRO E. 2016. Atividade reprodutiva de pei-
xes no arrasto camaroeiro: algo mudou após
dez anos? Monografia apresentada como
requisito parcial para obtenção do título de
Bacharel em Ciências Biológicas, Setor de
Ciências Biológicas, Universidade Federal do
Paraná. Curitiba, 46 p.
REIS EG, PAWSON MG. 1999. Fish morphology
and estimating selectivity by gillnets. Fish
Res. 39 (3): 263-273. doi:10.1016/S0165-
7836(98)00199-4
ROBERT MC, SOUZA MAM, CHAVES PTC. 2007.
Biologia de Paralonchurus brasiliensis
(Steindachner) (Teleostei, Sciaenidae) no lito-
ral sul do Estado do Paraná, Brasil. Rev Bras
Zool. 24: 191-198.
ROMERO RM, MORAES L, SANTOS M, ROCHA G,
CETRA M. 2008. Biology of Isopisthus parvip-
innis: an abundant sciaenid species captured
bycatch during sea-bob shrimp fishery in
Brazil. Neotrop Ichthyol. 6: 67-74.
SANTURTÚN M, PRELLEZO R, ARREGI L, IRIONDO
A, ARANDA M, KORTA M, ONAINDIA I, GARCIA
D, MERINO G, RUIZ J, ANDONEGI E. 2014.
179
CHAVES: JUVENILES AND UNDERSIZED FISH CAUGHT BY GILLNETS
Characteristics of multispecific fisheries in the
European Union. Directorate-General for
Internal Policies, Policy Department B: Struc-
tural and Cohesion Policies, Fisheries. Brus-
sels: European Parliament. 98 p.
SILVA-JÚNIOR CA, VIANA AP, FRÉDOU FL, FRÉDOU
T. 2015. Aspects of the reproductive biology
and characterization of Sciaenidae captured as
bycatch in the prawn trawling in the northeast-
ern Brazil. Acta Sci-Biol Sci. 37: 1-8. doi:10.
4025/actascibiolsci.v37i1.24962
SILVANO AM, HALLWASS G, JURAS A, LOPES PFM.
2016. Assessment of efficiency and impacts of
gillnets on fish conservation in a tropical
freshwater fishery. Aquat Conserv Mar
Freshw Ecosyst. doi:10.1002/aqc.2687
SOUZA LM, CHAVES P. 2007. Atividade reproduti-
va de peixes (Teleostei) e o defeso da pesca de
arrasto no litoral norte de Santa Catarina, Bra-
sil. Rev Bras Zool. 24: 1113-1121.
SUNIL MOHAMED K, ZACHARIA PU, MAH-
ESWARUDU G, SATHIANANDAN TV, ABDUS-
SAMAD EM, GANGA U, LAKSHMI PILLAI S,
SOBHANA KS, REKHA J, JOSILEEN J, et al. 2014.
Minimum Legal Size (MLS) of capture to
avoid growth overfishing of commercially
exploited fish and shellfish species of Kerala.
Mar Fish Info Serv T & E Ser. 220. 5 p.
WOLFF M, TAYLOR H, TESFAYE G. 2015. Implica-
tions of using small meshed gillnets for the
sustainability of fish populations: a theoretical
exploration based on three case studies. Fish
Manag Ecol. 22: 379-387. doi:10.1111/fme.
12137
180 MARINE AND FISHERY SCIENCES 35 (2): 165-180 (2022)