Percophis brasiliensis, Quoy & Gaimard, 1825, Quoy & Gaimard, 1825

Bauer, Arthur de Barros & Fischer, Luciano Gomes, 2024, Trophic ecology of the demersal predator Brazilian flathead Percophis brasiliensis (Percophidae) in a coastal upwelling ecosystem, SW Atlantic, Neotropical Ichthyology 22 (2), pp. e 230115-e 230115 : e230115-230115

publication ID

https://doi.org/10.1590/1982-0224-2023-0115

DOI

https://doi.org/10.5281/zenodo.15491860

persistent identifier

https://treatment.plazi.org/id/039D0429-CF2E-9F31-FE31-FB2DFBCEFE88

treatment provided by

Felipe

scientific name

Percophis brasiliensis
status

 

RESULTS View in CoL

Sea surface temperature (SST) data recorded by the data logger confirmed the presence of upwelling events throughout the sampling period ( Fig. S1 View FIGURE 1 ). The events occurred with greater intensity mainly in February, September and October with average temperatures close to 16°C.

Diet description. The non-empty stomachs corresponded to 49% (n = 496) of the total specimens collected and dissected (n = 1016) ( Tab. 1 View TABLE 1 ). Percophis brasiliensis ’ diet was composed of 37 prey taxa, of which 27 were identified at the species level ( Tab. 2 View TABLE 2 ). Teleostei was the most consumed prey group in %W for all ontogenetic groups, mainly composed of small pelagic fishes ( Clupeiformes ). The juveniles showed a higher percentage of Teleostei prey, 79.7%W, mainly composed by Engraulidae . For juveniles, crustaceans (mostly shrimps) and Cephalopoda (squids) represented 20.3%W of the prey. The importance of Teleostei is similar between young adults and adults (54.6 and 53.9%W, respectively), with an increase in crustaceans (27.0 and 15.5%W) and cephalopods (17.5 and 29.6%W).

We found significant differences among ontogenetic groups, seasons, and the interaction between these factors (PERMANOVA; p ≤ 0.03) ( Tab. 3 View TABLE 3 ). Dietary ontogenetic shifts have been detected but these changes vary according to the season. During Autumn and Winter, juveniles differed from young adults and adults (pairwise PERMANOVA; p ≤ 0.02). Only adults showed differences from the other two ontogenetic groups in the Summer (p ≤ 0.04). Juveniles and adults are different during Spring (p = 0.004), but we found no differences between juveniles and young adults, and young adults and adults (p = 0.10 and p = 0.49, respectively). Females (n = 348, 433.1 mm ± 69.2) were larger than males (n = 144, 365.2 mm ± 40.5; PERMANOVA, p = 0.001). However, no differences in diet were observed between males and females (Pseudo-F = 1.36, p = 0.33).

In juveniles, there was no significant differences in the diet throughout the year (p ≥ 0.081), while young adults’ diet differed among all seasons (p <0.01), except between winter and summer (p = 0.57) when similar %W of demersal fishes and non-identified fish were ingested ( Fig. 2 View FIGURE 2 ). During the autumn, P. brasiliensis fed on the small pelagic shrimp Peisos petrunkevitchi Burkenroad, 1945 , while in the spring demersalpelagic cephalopods were the main prey group. The diet of adults during autumn was significantly different from all other seasons (p <0.01). Adults and young adults consumed a high proportion (%W) of P. petrunkevitchi during the autumn ( Figs. 2–3 View FIGURE 2 View FIGURE 3 ). Besides, during the autumn, the ingested prey number was four to 29 times higher than in other seasons for juveniles and adults ( Tab. S2 View TABLE 2 ). Despite the increase in prey number intake mainly between March and April, this pattern is not reflected in the %BW values ( Fig. S3 View FIGURE 3 ). In all other seasons, larger fish have a more diverse diet ( Tab. S2 View TABLE 2 ).

Niche breadth of young adults and adults was smaller during Autumn, probably due to the large ingestion of a single species ( Tab. S2 View TABLE 2 ). For juveniles, the lowest calculated niche breadth was observed in Spring. In general, the niche breadth slightly decreases with growth, with mean values of standardized Levins’ index = 0.29, 0.27, and 0.26 in juveniles, young adults, and adults, respectively ( Tab. S2 View TABLE 2 ).

Stable Isotope Analysis. Percophis brasiliensis δ 13 C values ranged between -18.36 and -16.77 ‰, with a mean of -17.58 ± 0.26 ‰, while δ 15 N ranged between 11.91 and 14.29 ‰, with a mean of 13.52 ± 0.41 ‰ ( Tab. 4 View TABLE 4 ). Significant relationships were observed between δ 13 C (r 2 = 0.092, p = 0.030) and δ 15 N (r 2 = 0.645, p <0.001) versus total length ( Fig. 4 View FIGURE 4 ).

Based on the measured standard ellipse corrected for small sample size (SEAc), the isotopic niche width decreases with the increase in fish size. Juveniles showed the broader niche (0.37), followed by young adults (0.34) and adults (0.28). The overlap area between juveniles and young adults was 37%, between young adults and adults was 53%, and between juveniles and adults was 28% ( Fig. 5 View FIGURE 5 ).

TABLE 2 | Diet composition of ontogenetic groups of Brazilian flathead Percophis brasiliensis. SL = Average standard length (mm), and TW = Average weight of predators (g), %N = Percentage in number, %W = Percentage in weight, %F = Frequency of occurrence. NI = Not identified.

Prey Items Juveniles n = 124, SL = 292, TW = 137 Young adults n = 195, SL = 353, TW = 265 Adults n = 177, SL = 437, TW = 520
%W %F %N %W %F %N %W %F %N
Pelagic prey 42.06 38.71 62.67 54.02 38.95 74.78 63.48 46.33 88.96
Crustaceans 6.85 4.84 44.45 15.64 10.26 69.04 11.67 11.3 84.9
Peisos petrunkevitchi Burkenroad, 1945 6.57 3.23 43.83 15.64 10.26 69.04 10.89 10.17 79.83
Sergestidae NI 0.28 1.61 0.62 0 0 0 0.78 1.13 5.07
Fishes 27.8 25.8 15.13 20.9 18.97 4.16 22.24 18.06 2.28
Anchoa sp. 1.34 1.61 0.62 1.45 2.05 0.26 0.06 0.56 0.05
Anchovia clupeoides (Swainson, 1839) 0 0 0 0.29 0.51 0.07 0 0 0
Carangidae NI 0 0 0 0.65 0.51 0.07 1.1 1.13 0.09
Chirocentrodon bleekerianus (Poey, 1867) 1.71 1.61 0.62 8.54 4.62 0.72 0.58 1.13 0.09
Clupeidae NI 0 0 0 0 0 0 1.39 0.56 0.05
Clupeiformes NI 7.54 4.84 3.09 0.6 0.51 0.07 2.76 2.82 0.23
Engraulidae NI 17.21 17.74 10.8 8.5 9.23 2.64 1.87 6.78 1.23
Engraulis anchoita Hubbs & Marini, 1935 0 0 0 0.59 1.03 0.26 0.11 1.13 0.09
Harengula clupeola (Cuvier, 1829) 0 0 0 0 0 0 5.29 0.56 0.09
Lycengraulis grossidens (Spix & Agassiz, 1829) 0 0 0 0.28 0.51 0.07 0 0 0
Sardinella aurita Valenciennes, 1847 0 0 0 0 0 0 7.5 2.26 0.27
Trachurus lathami Nichols, 1920 0 0 0 0 0 0 1.58 1.13 0.09
Cephalopoda 7.41 7.26 3.09 17.49 11.28 1.58 29.57 20.33 1.78
Doryteuthis pleii (Blainville, 1823) 0.26 1.61 0.93 15.22 4.62 0.66 24.27 14.12 1.14
Doryteuthis sp. 6.85 2.42 0.93 1.33 2.05 0.26 3.94 2.82 0.23
Lolliguncula brevis (Blainville, 1823) 0 0 0 0.39 3.08 0.46 0.1 1.13 0.09
Teuthida NI 0.3 3.23 1.23 0.54 1.54 0.2 1.26 2.26 0.32
Benthic/Demersal prey 16.81 27.45 14.22 31.19 37.97 18.06 24.15 53.59 7.47
Crustaceans 6.07 16.13 7.41 11.36 19.99 9.03 3.82 17.49 4.12
Artemesia longinaris Bate, 1888 0 0 0 0.35 1.54 0.2 0.32 1.69 0.37
Brachyura NI 0 0 0 0.01 0.51 0.07 0 0 0
Dendrobranchiata NI 2.93 10.48 4.94 2.22 5.64 7.18 0.73 4.52 2.78
Farfantepenaeus sp. 0 0 0 1.15 1.03 0.13 1.19 1.13 0.09

TABLE 3 | PERMANOVA results of the main effects between the factors ontogenetic groups and seasons of Brazilian flathead Percophis brasiliensis, estimated from Bray-Curtis similarity matrix based on %W. Significantly differences (p <0.05) are presented in bold.

Source df MS Pseudo-F P(perm) Perm. (n)
Ontogenetic groups 2 16716 2.832 0.0288 9940
Season 3 19204 3.2602 0.0085 9941
Ontogenetic groups vs. Season 6 5946 1.5593 0.0176 9864
Residual 481 3813.3      
Total 492        

Kingdom

Animalia

Phylum

Chordata

Order

Perciformes

Family

Percophidae

Genus

Percophis

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