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Revista de Biología Tropical, ISSN: 2215-2075, Vol. 70: 541-556, Enero-Diciembre 2022 (Publicado Ago. 16, 2022)
Comparison of fish assemblages recorded by visual census and video census
Luis Gibran Juárez-Hernández1*; https://orcid.org/0000-0003-0658-6818
María Guadalupe Sánchez-Vega1; https://orcid.org/0000-0003-2852-9283
1. Centro Universitario Ciencia e Innovacción para la Formación y el Emprendimiento (CIFE). Calle Tabachín 514,
Bellavista, 62140 Cuernavaca, Morelos, México; gibbjuarez@gmail.com (Correspondence*),
lupitasanchez110406@gmail.com
Received 04-V-2022. Corrected 05-VIII-2022. Accepted 08-VIII-2022.
ABSTRACT
Introduction: Underwater visual censuses are the basis of many studies on fish ecology, however, a series of
limitations and errors influence the traditional visual estimation of fish richness and abundance. Video tech-
niques have been proposed to mitigate such errors, but there are few studies that compare the effectiveness of
both methods.
Objective: To compare the estimates obtained through the traditional census and the video census of the fish
community of two localities in the central Mexican Pacific.
Methods: We studied the fish community of two bays of Huatulco, Oaxaca, Mexico. We established sampling
points in each bay and applied a traditional census and a diver-operated video census. We used comparison tests
and analysis of similarity tests to compare richness, abundance and diversity by locality; and permutation tests
for the same parameters at each sampling point.
Results: Both censuses provide similar estimates regarding the richness, abundance, and diversity by locality
and by sampling points. There were no statistically significant differences between traditional census and a diver-
operated video census in terms of richness, abundance, and diversity.
Conclusions: Video census using the diver-operated video technique can be used as a complement or as an
alternative to traditional census. Its use can provide a more complete assessment, increase data acquisition,
and implement long-term monitoring programs in areas where there are economic limitations for its operation.
Key words: sampling methods; Maguey; Huatulco; ichthyofauna; Mexican Pacific.
https://doi.org/10.15517/rev.biol.trop.2022.48420
AQUATIC ECOLOGY
The underwater visual census forms the
basis of many studies on the ecology of fish in
fresh and marine shallow waters (Caldwell et
al., 2016; Samoilys & Carlos 2000). Since its
implementation in the 1950s, it has become the
preferred method for sampling reef fish com-
munities (Kulbicki et al., 2010; Pais & Cabral,
2017; Thanopoulou et al., 2018), as a result
of it being a non-destructive (Thanopoulou et
al., 2018; Widmer et al., 2019; Yulianto et al.,
2015) and inexpensive method (Holmes et al.,
2013; Watson & Quinn, 1997) that offers quick
estimates of the richness, the abundance, and
the sizes of fish (Samoilys & Carlos, 2000).
Although its use has spread, it is impor-
tant to note that it presents limitations for
its execution, related to environmental fac-
tors (depth, water clarity, weather conditions),
logistics (immersion time or sampling fre-
quency) (Emslie et al., 2018; Holmes et al.,
2013; Williams et al., 2006), influence of
the diver on the behavior of certain species
542 Revista de Biología Tropical, ISSN: 2215-2075 Vol. 70: 541-556, Enero-Diciembre 2022 (Publicado Ago. 16, 2022)
(attraction or repulsion) (Dickens et al., 2011;
Pais & Cabral, 2017; Pereira et al., 2016) and
error pathways, being these related to the diver
(experience, ability, and behavior) (Assis et al.,
2013; Bozec et al., 2011; Widmer et al., 2019),
erroneous identification of the species, under-
estimating the abundance of small and cryptic
species (Willis, 2001) and overestimating the
most abundant (Williams et al., 2006), which
influence the estimation of the richness and
abundance (Brock, 1982; García-Charton et
al., 2000) and therefore may compromise the
ability to detect significant changes in the fish
community (Langlois et al., 2010; Wakefield
et al., 2013).
Regarding the afore mentioned, the imple-
mentation of techniques based on video has
been proposed (Langlois et al., 2010; Mallet &
Pelletier, 2014). Although the development of
video sampling methodologies for the study of
marine communities dates back to the 1950s,
there were several limitations (cost and low
operation of the equipment, battery autonomy,
storage capacity) (Bacheler et al., 2017; Wid-
mer et al., 2019), these have been overcome as
a result of technological progress (greater oper-
ability, autonomy and capacity) and that are
economically more affordable (Goetze et al.,
2019; Mallet & Pelletier, 2014; Zarco-Perello
& Enríquez, 2019).
With regards to its advantages, it is speci-
fied that they allow to reduce the error related
to the variability between observers, since the
information can be verified (Assis, 2013; Lan-
glois et al., 2010; Widmer et al., 2019). It´s a
permanent record, it allows to re-examine the
data for various purposes (Goetze et al., 2019;
Pelletier et al., 2011; Tessier et al., 2013), and
it allows to collect field data by divers who are
not experts in fish identification (Pelletier et al.,
2011; Tessier et al., 2005; Tessier et al., 2013).
Operationally, among its disadvantages are
the cost of the equipment, complications for its
execution (Holmes et al., 2013; Widmer et al.,
2019), the precision with respect to the human
eye (Bortone et al., 2000; Holmes et al., 2013;
Tessier et al., 2005), as well as the limitation
to identify small and cryptic species (Goetze
et al., 2019; Grane-Feliu et al., 2019; Wilson
et al., 2018). Other aspects that have been
mentioned are that it can be more expensive
and slower than the traditional census since it
involves video processing for analysis (Grane-
Feliu et al., 2019; de la Guardia et al., 2021;
Holmes et al., 2013).
Within the video method, the most recog-
nized techniques are stationary (with bait or
without bait), diver-operated video (DOV), and
remote underwater video (Mallet & Pelletier,
2014; Schramm et al., 2020; Wilson et al.,
2018). According to Murphy & Jenkins (2010)
as well as Goetze et al. (2015) report that each
technique offers advantages and disadvantages.
Of these techniques, those operated by divers
(DOV) stand out, since they are considered the
most profitable for estimating the abundance
and richness of fish communities (Goetze et al.,
2015; Grane-Feliu et al., 2019; Langlois et al.,
2010; Wilson et al., 2018). Watson et al. (2005)
refers that this technique allows greater maneu-
verability of the camera(s), which offers advan-
tages in structurally complex habitats such as
coral reefs. Likewise, it is specified that this
technique is the most pertinent when there is
an interest in the associations of fish with a par-
ticular type of habitat or physical structure due
to the ability to restrict the size of the sample
unit (Galaiduk et al., 2017; Tessier et al., 2013).
This technique consists in the use of a
video camera(s) to record the route that is made
in the sampling unit, the identification of the
species and registration of their abundance is
carried out later by viewing the recording on a
computer monitor (Goetze et al., 2015). Within
the DOV, two variations are recognized, the first
is the use of a single camera where the tech-
nique consists of the video operator swimming
alongside the diver who performs the census
(Bortone et al., 1991; Pelletier et al., 2011; Tes-
sier et al., 2005), and the second consists of a
system where two cameras are mounted on a
base (stereo video) (S-DOV) and in the same
way the video operator swims next to the diver
who performs the census (Goetze et al., 2015;
Harvey et al., 2001; Harvey et al., 2004; Lan-
glois et al., 2010).
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Taking them into account, studies that
have compared the traditional census with the
S-DOV are frequent (Grane-Feliu et al., 2019;
de la Guardia et al., 2021; Wilson et al., 2018),
this is not the case for studies that compare the
DOV with the traditional one (Bortone et al.,
1991; Tessier et al., 2005; Tessier et al., 2013;
Wartenberg & Booth, 2015). These studies
coincide that through both methods they can
provide comparable estimates, however, it is
emphasized that a greater number of species
and individuals are recorded through the tradi-
tional census.
In this regard, it should be noted that the
implementation of the diver-operated video
technique to evaluate ichthyofauna in the Mexi-
can Pacific is limited, and there is no informa-
tion on its use. Therefore, the present objective
is to compare the estimates obtained through
the traditional census and the video census of
the fish community of two localities in the cen-
tral Mexican Pacific.
MATERIALS AND METHODS
Study area: The localities selected to
carry out the study were Maguey and La
Entrega bays, which are located in the complex
“Huatulco Bays” (15°40’48” - 15°45’36” N
& 96°14’24” - 96°07’13” W), on the coast
of the state of Oaxaca, Mexico (Fig. 1). This
area is considered one of the most important
regions in the reef ecosystems of the Mexican
Pacific, since it is home to a great diversity
of species of echinoderms, corals, and fishes
(Juárez-Hernández & Tapia-García 2017;
Juárez-Hernández & Tapia-García, 2018a;
López-Pérez et al., 2014). Both bays are char-
acterized by high species richness, abundance,
Fig. 1. Location of the study area “Huatulco Bays”. Distribution of sampling points in A. Maguey Bay and B. La Entrega
Bay.
544 Revista de Biología Tropical, ISSN: 2215-2075 Vol. 70: 541-556, Enero-Diciembre 2022 (Publicado Ago. 16, 2022)
and fish diversity (Juárez-Hernández & Tapia-
García, 2017; Juárez-Hernández et al., 2021;
López-Pérez et al., 2010).
Sampling strategy: The sampling was
carried out in September 2019, and the selec-
tion of the sampling sites in each locality corre-
sponded to previous studies (Juárez-Hernández
& Tapia-García, 2017; Juárez-Hernández et al.,
2021). Specifically for Maguey, nine sampling
points were selected and eight for La Entrega.
These points covered environments with rocky
substrate (M1, E1), coral (M7, E3, E4, E5; E6,
E7), coral rubble (E8), sand (M4, M5) as well
as mixed environments, such as coral-rocky
(M3, M8), rocky-coral (M2, M9) and sandy-
rocky-mixed (M6) (Fig. 1). The depth at these
sampling points was at least 3 m and the maxi-
mum was 10 m.
At each sampling point, a 10 meter long
transect was established, in which the tradi-
tional census (TC) and the video census (VC)
were carried out using the diver-operated video
technique (DOV) by the same subject using
free diving (snorkel) (Fig. 2). Therefore, the
video camera was placed in the visor of the
observer, which is designed for this purpose.
The equipment used to record was a Mobo
action camera, model 9031 and the camera
parameters were 4K recording (Ultra High
Definition- 3840x2160) without any zoom. It
is required that the observer be trained in the
identification of the fish species and the execu-
tion of the method.
The procedure consisted of the observer
standing at one end of the transect, recording
the transect number on an acrylic table, and
then turning on the camera and recording the
transect number annotation. In this way, the
recording began as the observer recorded the
species and their abundance on the acrylic
table. In each transect three routes were made,
10 meters each (Fig. 2), the first was to the
opposite end of the transect (near the surface)
(Fig. 2A), then back to the point of origin (mid-
water) (Fig. 2B), and finally a third route to the
opposite end of the transect (near the bottom)
(Fig. 2C). At the end of the routes, both the
recording of fish in the acrylic table, as well
as the recording, stopped. The duration of the
routes was approximately five minutes.
The videos were viewed two months after
sampling on a 23-inch monitor. The analysis of
the video was similar to the in-situ procedure
carried out in the traditional census, that is, at
the beginning of the video the species and num-
ber of individuals were recorded on a sheet of
paper. It is specified that the video was played
continuously and without pauses, for a total of
five minutes.
Fig. 2. Representation of the routes made at each sampling point. A. near the surface, B. mid-water and C. near the bottom.
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Data analysis: The taxonomic status of
the species was verified according to Fricke et
al. (2020a) and the taxonomic arrangement was
based on Fricke et al. (2020b). For each of the
censuses (TC and VC), on each sampling point
and locality, the number of species, abundance
(number of individuals), and diversity (Shan-
non & Wiener, 1963) were calculated. Species
accumulation curves were performed using the
non-parametric estimator (Chao 1) based on
abundance. The curves were constructed with
9 000 randomizations using the EstimateS v9
packet (Colwell, 2013).
For each locality, the results of each cen-
sus were compared using a qualitative simi-
larity coefficient (Sorensen). The degree of
agreement between the observations of both
censuses was evaluated by means of Kend-
all’s W concordance coefficient (Kendall &
Smith, 1939; Legendre, 2005). Paired t-tests
were carried out to compare the number of
species, abundance, and diversity by type of
census in each locality, when the normality
assumption was fulfilled (Shapiro-Wilk test,
P > 0.05), and if this assumption was not test-
able, the Wilcoxon test was applied (Whitlock
& Schluter, 2009). To compare the number of
species, abundance, and diversity of the same
sampling site (environment) by type of census,
permutation tests were used. This test calcu-
lates the richness, abundance, and diversity
for two samples and compares each of these
parameters using permutations (9999) (Ham-
mer, 2021). In addition, a meta-analysis was
carried out (Sokal & Rohlf, 1995) considering
the p values of each of these tests with the
objective of verifying if there were differ-
ences in the number of species, abundance and
diversity between census type by locality. For
this analysis it was taken into account that if
the resulting value of the product of the meta-
analysis (-2 Σ Ln P) was greater than the value
of the Chi-square statistic (α = 0.005 with 2*k
degrees of freedom), there were differences
between the attribute analyzed (number of spe-
cies, abundance, diversity) by type of census.
The evaluation of the degree of similarity of the
ichthyofauna between the types of census was
carried out using the Bray-Curtis index (Clarke
& Warwick, 1994), and its analysis was carried
out by a Non-metric Multidimensional Scaling
(nmMDS) and analysis of similarity (ANO-
SIM) (Clarke, 1993) with permutation (9999)
to identify significant differences in terms of
composition and abundance of fish. If the simi-
larity analysis revealed differences, a similarity
percentage analysis (SIMPER) (Clarke, 1993)
was performed to identify the species that con-
tribute to the differentiation between both types
of censuses (TC vs VC). Finally, the abundance
of the most represented species was compared
between both types of censuses (TC vs VC)
using paired t-tests, or, when appropriate, using
the Wilcoxon test. All tests and analyzes were
carried out with the Past V.4.5 packet (Hammer
et al., 2001).
RESULTS
Maguey Bay: In the traditional census
(TC), 27 species (Mean = 7.25 ± 3.32) cor-
responding to 21 genera, 13 families, and
seven orders were identified (Table 1). The
total abundance was 235 individuals (Mean =
9.37 ± 15.68), the diversity was 2.172 (Mean
= 1.41 ± 0.38) (Fig. 3). According to the Chao
1 estimator, the expected number of species
was 33. Stegastes acapulcoensis, Thalassoma
lucasanum and Microspathodon dorsalis were
the most abundant species.
In the video census (VC), 21 species
(Mean = 6.5 ± 2.56) corresponding to 16 gen-
era, 10 families and five orders were identified
(Table 1). The abundance was 203 individuals
(Mean = 24.62 ± 10.62), the diversity was
1.969 (Mean = 1.38 ± 0.42) (Fig. 3). Accord-
ing to the Chao 1 estimator, the expected
number of species was 23. S. acapulcoensis,
T. lucasanum and M. dorsalis were the most
abundant species.
The species that were only identified
using the traditional method were: Arothron
meleagris, Canthigaster punctatissima, Epi-
nephelus labriformis, Fistularia commersonii,
Halichoeres chierchiae, H. nicholsi, Johnran-
dallia nigrirostris, Kyphosus vaigiensis and
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TABLE 1
Taxonomic list of the fish community of Maguey and La Entrega bays
Class Order Family Species Maguey Entrega
TC VC TC VC
Actinopteri Syngnathiformes Fistularidae Fistularia commersonii Rüppell, 1838 1 1 1
Carangiformes Carangidae Caranx caballus Günther, 1868 5 1
Caranx caninus Günther, 1867 2 5
Trachinotus rhodopus Gill, 1863 4 3
Mugiliformes Mugilidae Mugil curema Valenciennes, 1836 7 1
Acanthuriformes Pomacanthidae Holacanthus passer Valenciennes, 1846 3322
Chaetodontidae Chaetodon humeralis Günther, 1860 2
Johnrandallia nigrirostris (Gill, 1862) 1 3 2
Acanthuridae Acanthurus xanthopterus Valenciennes, 1835 2 5
Prionurus laticlavius (Valenciennes, 1846) 11 13 9 14
Tetraodontiformes Tetraodontidae Arothron meleagris (Anonymous, 1798) 1 6 7
Canthigaster punctatissima (Günther, 1870) 1
Ostraciidae Ostracion meleagris (Shaw, 1796) 1
Balistidae Sufflamen verres (Gilbert and Starks, 1904) 1 2
Centrarchiformes Kyphosidae Kyphosus elegans (Peters, 1869) 7 1
Kyphosus vaigiensis (Quoy and Gaimard, 1825) 2 1 2
Cirrhitidae Cirrhitichthys oxycephalus (Bleeker, 1855) 3
Perciformes Serranidae Cephalopholis panamensis (Steindachner, 1877) 3 2
Epinephelus labriformis (Jenyns, 1840) 1 1
Lutjanidae Lutjanus argentiventris (Peters, 1869) 3 2
Mullidae Mulloidichthys dentatus (Gill, 1863) 1 2
Pomacentridae Abudefduf concolor (Gill, 1862) 3 2
Abudefduf troschelii (Gill, 1862) 2 2 3
Azurina atrilobata (Gill, 1862) 10 4
Microspathodon bairdii (Gill, 1862) 1711
Microspathodon dorsalis (Gill, 1862) 24 27 7 11
Stegastes acapulcoensis (Fowler, 1944) 94 81 84 68
Stegastes flavilatus (Gill, 1862) 141
Labridae Bodianus diplotaenia (Gill, 1862) 6443
Halichoeres chierchiae Di Caporiacco, 1948 1
Halichoeres dispilus (Günther, 1864) 2 1
Halichoeres nicholsi (Jordan and Gilbert, 1882) 1 2
Halichoeres notospilus (Günther, 1864) 2 4
Thalassoma lucasanum (Gill, 1862) 43 30 105 96
Scaridae Scarus ghobban Forsskål, 1775 1
Scarus perrico Jordan y Gilbert, 1882 2 5
Species registered in the traditional census (TC) and video census (VC) in in each locality.
Sufflamen verres. For their part, the species
that were only identified by video were Cir-
rhitichthys oxycephalus, Kyphosus elegans and
Stegastes flavilatus. Through the video census,
77 % of the species observed by the traditional
census were recorded.
The species similarity between both meth-
ods was 75 % (Sorensen). The degree of
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agreement between observers was substantial
(W = 0.766, P = 0.029). Number of species (t
= 0.8143, P = 0.4422), abundance (t = 1.1232,
P = 0.2983) and diversity (t = 0.2897, P =
0.7804) did not show differences between the
type of census, as well as by environment (P
> 0.05) According to the meta-analysis, the
number of species (10.80 < 37.2), abundance
(30.80 < 37.2) and diversity (14.10 < 37.2)
showed no differences between census types.
The non-metric scaling showed the similarity
of the ichthyofauna recorded by both censuses
(traditional and video) both by sampling point,
as well as in a general way (Fig. 4A). Regard-
ing composition and abundance, no differences
were found (ANOSIM = -0.078, P = 0.8914).
The abundance of the dominant species did
not show differentiation (S. acapulcoensis: t =
0.759, P = 0.461), (T. lucasanum: t = 0.853, P
= 0.418), (M. dorsalis: W = 13.5, P = 0.092).
La Entrega Bay: In the traditional census
(TC), 20 species (Mean = 6 ± 3.03) belonging
to 16 genera, 12 families, five orders were
identified (Table 1). The total abundance was
239 individuals (Mean = 29.87 ± 12.33), the
diversity was 1.601 (Mean = 1.21 ± 0.486)
(Fig. 2). According to the Chao 1 estimator,
the expected number of species was 23.5. T.
lucasanum, S. acapulcoensis and P. laticlavius
were the most abundant species.
On the other hand, the video census (VC)
identified 18 species (Mean = 5.12 ± 3.39)
belonging to 16 genera, 11 families, five orders
were identified (Table 1). The abundance was
225 individuals (Mean = 28.125 ± 8.166), the
diversity was 1.741 (Mean = 1.13 ± 0.53) (Fig.
2). According to the Chao 1 estimator, the
expected number of species was 19. T. lucasa-
num, S. acapulcoensis and P. laticlavius were
the most abundant species.
The species that were only identified
by the traditional method were Halichoeres
nicholsi, Kyphosus elegans, Microspathodon
bairdii, Ostracion meleagris, Scarus ghob-
ban and Sufflamen verres. The species that
Fig. 3. Variation of the number of species, abundance, and diversity between the traditional census (TC) and video census
(VC) in each locality.
548 Revista de Biología Tropical, ISSN: 2215-2075 Vol. 70: 541-556, Enero-Diciembre 2022 (Publicado Ago. 16, 2022)
were only identified through the video census
were Abudefduf troschelii, Chaetodon hume-
ralis, Epinephelus labriformis and Kyphosus
vaigiensis. Through the video, 90 % of the
species observed by the traditional census were
recorded.
The species similarity between both meth-
ods was 78 % (Sorensen). The degree of agree-
ment between observers was very high (W
= 0.803, P = 0.036). Number of species (t =
1.433, P = 0.1949), abundance (W = 22.5, P =
0.5281) and diversity (t = 0.870, P = 0.4129)
did not show differences between the type of
census, as well as by environment (P > 0.05).
The meta-analysis corroborated these results,
as it showed that the number of species (12.86
< 34.26), abundance (22.76 < 34.26) and diver-
sity (14.90 < 34.26) were not different between
census types. Through non-metric scaling,
the similarity of the ichthyofauna recorded
by both censuses (traditional and video) was
observed both by sampling point, as well as in
a general way (Fig. 4B). In the same way, the
composition and abundance did not show dif-
ferences between the type of census (ANOSIM
= -0.05497, P = 0.8197). The abundance of
the dominant species did not show differentia-
tion (T. lucasanum: t = 0.4269, P = 0.682), (S.
acapulcoensis: t = 2.116, P = 0.109), (P. lativ-
lavius: W = 2, P = 0.654).
DISCUSSION
According to the results, it is specified that
the similarity of species between both tech-
niques in each locality was high (more than 70
%), as well as that related to orders, families,
genera, and dominant species. Regarding the
comparison of the composition and structure,
number of species, abundance and diversity
of the fish community and dominant spe-
cies between both methods, no significant
Fig. 4. Non-metric multidimensional scaling of sampling points carried out using the traditional census (solid line) and video
census (punctuated line) in A. Maguey Bay and B. La Entrega Bay.
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differences were found in each locality, which
is different to studies that have used a tech-
nique similar to the one presented here (DOV)
(Pelletier et al., 2011; Tessier et al., 2005;
Tessier et al., 2013), but it is similar to that
reported by Bortone et al. (1991) as well as
Wartenberg & Booth (2015) who used the
same technique, as well as other works that
used the S- DOV (Grane-Feliu et al., 2019; de
la Guardia et al., 2021).
Probably no significant differences will
be found, it is the result of the way in which
the chosen technique (DOV) was implemented
as well as the technique itself, conjoined with
the experience of the observer both in the iden-
tification of the fish, as well as in the execu-
tion of the census (traditional and by video).
Regarding its execution, the observer who
registered the species is the same one who car-
ried out the recording and analysis of it, which
determines that there is a high concordance
between observations, which is different from
the way in which it was carried out in other
works that have used the DOV (Bortone et al.,
1991; Pelletier et al., 2011; Tessier et al., 2005;
Tessier et al., 2013), since they used a second
observer to record the video. Regarding the
chosen technique, compared to other video
techniques, it allows greater maneuverability
of the camera(s), which offers advantages in
structurally complex habitats such as coral
reefs (Watson et al., 2005). This allowed for
an adequate characterization of the fish com-
ponents (surface, mid-water, and bottom), and
of particular of the cryptic fish component, for
which the third route was carried out, which is
recommended to adequately characterize this
component (Holmes et al., 2013; Pelletier et al.,
2011; Watson et al., 2005).
One aspect that was considered to cause
differences in the number of species, abun-
dance and diversity between both techniques
was the complexity of the habitat (determined
by the combination of substrates, number of
coral species, depth, or exposure to waves)
for certain environments, which are charac-
terized by presenting a greater number of
fish species and abundance (Juárez-Hernández
& Tapia-Garcia, 2018a; Juárez-Hernández &
Tapia-Garcia, 2018b; Juárez-Hernández et al.,
2013). Specifically, in Maguey Bay these envi-
ronments are the mixed, coral, and rocky-coral
environments (Juárez-Hernández et al., 2021),
and in La Entrega the coral and rubble-sandy
environments (Juárez-Hernández, 2014), how-
ever, it was found that there were no significant
differences in the community parameters ana-
lyzed in the mentioned environments, as well
as for the rest of the environments.
Given these results, it can be specified that
the DOV technique provides comparable esti-
mates of richness and abundance with respect
to the traditional census, coinciding with that
reported by Bortone et al. (1991) as well as
Wartenberg & Booth (2015), revealing that the
DOV can be considered as a complementary
technique and/or equivalent to the traditional
census (Davis et al., 2014; Wartenberg &
Booth, 2015). Similar conclusions have been
obtained using the S-DOV technique (Grane-
Feliu et al., 2019; de la Guardia et al., 2021;
Wilson et al., 2018).
Considering its complementary character
for Maguey Bay, combining the information
from both techniques provides a total of 29 spe-
cies, this estimate being similar to that obtained
by Juárez-Hernández et al. (2013), in which the
sampling effort was higher (15 transects) than
that carried out here. In La Entrega, when com-
bining the information, it provides a total of
23 species, this estimate being higher than that
obtained in a sampling carried out in Septem-
ber 2010 with the same sampling effort (nine
transects) (Juárez-Hernández, 2014). It should
be noted that both mentioned studies used two
observers and transects of the same length as
the ones used in this study.
In addition to the aforementioned, the use
of this technique as a complement has sev-
eral advantages, one of which is that it offers
a permanent record, allowing the correction
of misidentified in situ species (Bortone et
al., 1991; Langlois et al., 2010; Wartenberg
& Booth, 2015), it limits the potential effects
of the observer, since the video can be viewed
and examined repeatedly by different people
550 Revista de Biología Tropical, ISSN: 2215-2075 Vol. 70: 541-556, Enero-Diciembre 2022 (Publicado Ago. 16, 2022)
(Langlois et al., 2010; Pelletier et al., 2011;
Preuss et al., 2009), it provides additional infor-
mation, since the characteristics of the habitat
are recorded on the video (Pelletier et al., 2011;
Tessier et al., 2013; Wilson et al., 2018). This is
essential since many times the observer, being
focused on registering and counting the fish,
is not able to adequately characterize the reef
architecture and the attributes associated with it
(Preuss et al., 2009; Tessier et al., 2013; Wart-
enberg & Booth, 2015).
The disadvantages of video methods have
been stipulated to be the cost associated with
purchasing the equipment as well as the addi-
tional time it takes to process and analyze the
recording (Goetze et al., 2019; de la Guardia
et al., 2021; Tessier et al., 2013). Regarding
the cost of the equipment used for this study,
it is specified that it was low (<$100 dollars),
highlighting the role of action cameras, which
offer a perfect balance among price, image
quality, and operability (Letessier et al., 2015;
Zarco-Perello & Enríquez, 2019), thus granting
viability and accessibility (Goetze et al., 2015;
Letessier et al., 2015). In relation to the proce-
dure, processing and analyzing the recording,
as well as the execution of the census and its
analysis in the study, did not last more than
five minutes and it should be clarified that the
video was not edited so it was viewed exactly
as it was recorded. Whereas these aspects allow
us to consider this technique as profitable,
coinciding with what has been described by
various authors (Grane-Feliu et al., 2019; Lan-
glois et al., 2010; Tessier et al., 2005), it is vital
to mention that a more detailed analysis of the
recording (setting a longer time for its analysis)
would provide valuable additional information.
Considering all these elements, it can
be indicated that the combination of both
techniques could provide a more complete
evaluation and a permanent record of all fish
(Grane-Feliu et al., 2019; de la Guardia et
al., 2021; Wartenberg & Booth, 2015), which
undoubtedly can increase the spatial and
temporal scope of the monitoring programs,
potentially improving the understanding of the
environmental and anthropogenic changes in
fish communities (Wilson et al., 2018). The
foregoing is highly significant in reef systems
given their current situation (Hoegh-Guldberg
et al., 2017; Hughes et al., 2017), since, if
biodiversity is to be conserved, it is necessary
to evaluate it in an adequate and representative
way through a census (Jackson et al., 2001;
Wilson et al., 2018) using an appropriate sur-
vey method (Rotherham et al., 2007; Thomas,
1996; Wartenberg and Booth, 2015).
Although the differences were not signifi-
cant, it is denoted that using of the TC a greater
number of species and abundance were reg-
istered, which is consistent with other studies
that have used the DOV (Bortone et al., 2000;
Pelletier et al., 2011; Tessier et al., 2005), as
well as other video techniques (S-DOV) (Davis
et al., 2014; de la Guardia et al., 2021; Wilson
et al., 2018). The fact that a greater number of
species and abundance is recorded has been
explained under various points, the first of
which is that the field of view of the camera is
smaller than that of the observer (Bortone et al.,
2000; Tessier et al., 2013; Widmer et al., 2019),
that the definition capacity of the human eye is
greater than that of the video camera (Holmes
et al., 2013; Lowry et al., 2012; Wilson et al.,
2018), and that the identification of the species
in a video projected on a screen is more com-
plex because the resolution is lower than that
of the human eye (de la Guardia et al., 2021;
Pelletier et al., 2011). These conditions, at first,
would limit the equivalent character, as referred
by Tessier et al. (2005), however, with techno-
logical advancement and multiple options and
configurations of action cameras (Goetze et
al., 2015; Goetze et al., 2019; Zarco-Perello &
Enríquez, 2019), these limitations can be over-
come, and therefore, their equivalence char-
acter could be established (Grane-Feliu et al.,
2019; de la Guardia et al., 2021; Wartenberg &
Booth, 2015).
Another aspect that has been referred to is
that indicated by Bortone et al. (1991) as well as
by Tessier et al. (2013) who refer that the reason
why a greater number of species are identified
by TC is that unlike the camera, the observer
can turn his head to survey fish. However, with
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Revista de Biología Tropical, ISSN: 2215-2075, Vol. 70: 541-556, Enero-Diciembre 2022 (Publicado Ago. 16, 2022)
the technique used here, since the camera is
attached to the observer’s visor, it rotates in the
direction where the observer’s view is directed.
Although this is an advantage, it must be speci-
fied that in some cases in the present study it
resulted in an inconvenience, since the used
camera does not have an image stabilization
system, determining that when the observer
made “sudden” movements to observe species,
the image is destabilized, limiting the identifi-
cation of the species and the recording of their
abundance. Probably this situation determined
that in Maguey the percentage of species that
were recorded in the video was lower (77 %)
than in the traditional census. This compared to
La Entrega, which through the video recorded
90 % of the species in comparison to the tradi-
tional census. The foregoing refers to the fact
that the environments of Maguey, unlike La
Entrega, are characterized by having a greater
structural complexity, meaning that they pres-
ent a greater number of species and abundance
(Juárez-Hernández, 2014; Juárez-Hernández
& Tapia-García, 2017), which within the sam-
pling determined to carry out a greater number
of movements, causing the loss of stability of
the video and therefore limiting the identifi-
cation of the species. To reduce this effect, it
is necessary to purchase a camera that has an
electronic stabilization system.
Video techniques have been established
to be deficient in identifying small and cryptic
species (de la Guardia et al., 2021; Holmes et
al., 2013; Wilson et al., 2018). In this order,
for Maguey Bay of the eight species not iden-
tified through the video, only three of these
are considered cryptic or associated with the
substrate (Halichoeres chierchiae, H. nicholsi
and Epinephelus labriformis) (Robertson &
Allen, 2015), while for La Entrega, only four
species were not identified through the video
(Table 1), being H. nicholsi the only of these
considered as cryptic. As it can be seen, only
a minimal percentage of the species referred
to as cryptic was not observed through the
video, which may be the result of the technique
used (DOV) and the third route, which is pre-
cisely designed to characterize the cryptic or
components associated to the bottom (Holmes
et al., 2013; Pelletier et al., 2011; Watson et
al., 2005). In accordance with this argument,
it is noted that only with the video the species
Cirrhitichthys oxycephalus was recorded in
Maguey, which has been referred to as cryptic
and small (Juárez-Hernández & Tapia-Garcia,
2018b; Robertson & Allen 2015; Thomson et
al., 2000), while for La Entrega only with the
video were Chaetodon humeralis and Epineph-
elus labriformis registered, both associated
with the substrate (Robertson & Allen, 2015).
Species of other components (Abudefduf tros-
chelii y Kyphosus elegans) (Robertson & Allen,
2015), were only recorded through video and
not through TC, this is the result of the time
allocated by the observer to record the spe-
cies and its abundance in the acrylic, which is
consistent with what was reported by Tessier et
al. (2013), who referred that with a lot of infor-
mation to write at the same time (species and
their abundance), the risk of losing information
increases, therefore the use of audio recording
was recommended instead of performing the
annotations on acrylic (Bortone et al., 1991).
According to this point, the value of the video
recording is denoted, eliminating this problem
(Langlois et al., 2010; Watson et al., 2005; Wat-
son et al., 2010).
An aspect to highlight of the technique
used here that would reveal its high signifi-
cance is that it can be carried out by an
observer who is not an expert in fish identi-
fication (Mallet & Pelletier, 2014; Pelletier et
al., 2011; Wartenberg & Booth, 2015), which
determines that this is a profitable technique,
since it would allow simultaneous studies to
be carried out in different places (Mallet &
Pelletier, 2014; Tessier et al., 2013; Wilson et
al., 2018). In this regard, volunteers have been
posited as a significant source of help in col-
lecting marine biodiversity information, as it is
a cost-effective way to fill spatial and temporal
gaps in traditional monitoring programs (Edgar
et al., 2014; Lamine et al., 2018). Although this
could be feasible, it is necessary to emphasize
that the method must be easy to apply (Lamine
et al., 2018) and that the volunteers must be
552 Revista de Biología Tropical, ISSN: 2215-2075 Vol. 70: 541-556, Enero-Diciembre 2022 (Publicado Ago. 16, 2022)
given training on the characteristics of the sam-
pling, behavior, performance, specifications
on routes and sampling time (Aburto-Oropeza
et al., 2015; Edgar et al., 2014; Lamine et al.,
2018). Therefore, the technique implemented
here could be feasible in these terms, since the
equipment is inexpensive, the method is easy to
apply, and the training would be minimal, How-
ever, it is emphasized that when carried out by
free diving (snorkeling), its implementation
is limited to shallow areas. Considering these
points, the implementation of this technique in
the study area could be functional for the estab-
lishment of long-term monitoring programs
with the help of volunteers (Harvey et al., 2013;
Wilson et al., 2018).
The development of biotic inventories and
the quantification of biodiversity are essential
for the to the development and application of
relevant and successful management and con-
servation strategies (López-Pérez et al., 2013;
Lubchenco & Grorud-Colvert, 2015; Perrings
et al., 2011). Therefore, it is essential to explore
and implement profitable methods and tech-
niques that allow the fulfillment of such objec-
tives in an adequate and representative manner.
According to the above, the technique used
in the present study can be considered under
these characteristics, highlighting the two men-
tioned ways of use, the first being called as a
complement and the second as being called
equivalence that could be of high value. The
technique, being economical and easy to exe-
cute, could be functional in those areas where
the monitoring programs present problems for
their operation resulting from limitations in
their resources (material and human).
Ethical statement: the authors declare
that they all agree with this publication and
made significant contributions; that there is no
conflict of interest of any kind; and that we fol-
lowed all pertinent ethical and legal procedures
and requirements. All financial sources are
fully and clearly stated in the acknowledge-
ments section. A signed document has been
filed in the journal archives.
ACKNOWLEDGMENTS
To the anonymous reviewers for their valu-
able comments and observations.
RESUMEN
Comparación de ensamblajes de peces registrados
por censo visual y censo por video
Introducción: Los censos visuales submarinos son la base
de muchos estudios sobre ecología de peces, sin embargo,
una serie de limitaciones y errores influyen en la estima-
ción visual tradicional de la riqueza y abundancia de peces.
Se han propuesto las técnicas de video para mitigar tales
errores, pero existen pocos estudios que comparen la efec-
tividad de ambos métodos.
Objetivo: Comparar las estimaciones obtenidas mediante
el censo tradicional y el video censo de la comunidad de
peces de dos localidades del Pacífico central mexicano.
Métodos: Se estudió la comunidad de peces de dos bahías
de Huatulco, Oaxaca, México. Se establecieron puntos de
muestreo en cada bahía y se aplicó el censo tradicional
y video censo operado por buzo. Se emplearon pruebas
de comparación y análisis de pruebas de similitud para
comparar riqueza, abundancia y diversidad por localidad;
y pruebas de permutación para los mismos parámetros en
cada punto de muestreo.
Resultados: Ambos censos proporcionan estimaciones
similares en cuanto a la riqueza, abundancia y diversidad
por localidad y por punto de muestreo. No existieron dife-
rencias estadísticamente significativas entre el censo tradi-
cional y video censo operado por buzo respecto a riqueza,
abundancia y diversidad.
Conclusiones: El video censo mediante la técnica de video
operado por buzo puede utilizarse como complemento o
como alternativa al censo tradicional. Su uso puede pro-
porcionar una evaluación más completa, aumentar la adqui-
sición de datos e implementar programas de monitoreo a
largo plazo en áreas donde existen limitaciones económicas
para su operación.
Palabras clave: métodos de muestreo; Maguey; Huatulco;
ictiofauna; Pacífico mexicano.
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