Notes on Some Brazilian Anchovies (Family Engraulidae) with Descriptions of Four New Species

Hildebrand, Samuel F.; Carvalho, João de Paiva

doi:10.2307/1438718

Cited by 5 publications

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“…Anchoviella victoriae Hildebrand & de Carvalho, 1948: 292 (type locality: Vitória, State of Espírito Santo, Brazil); Carvalho, 1951: 51, figure 1 (list of Brazilian species of Anchoviella ); Santos, 1952: 75 (list of marine fishes of Brazil); Whitehead, 1973: 161 (junior synonym of A. cayennensis ); Menezes, 1974: 216 (holotype information); Whitehead et al ., 1988: 330 (junior synonym of A. cayennensis ).…”

Section: Resultsmentioning

confidence: 99%

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Redescription of Anchoviella cayennensis (Puyo, 1945) (Clupeiformes: Engraulidae), with the synonymization of Anchoviella sanfranciscana Barbosa, Gomes da Silva, da Rocha Araújo & Carvalho, 2017 and remarks on Anchoviella perfasciata (Poey, 1860)

Agostinho

Loeb

Dario

2022

Journal of Fish Biology

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Anchoviella cayennensis (Puyo, 1945) is a relatively small-sized, coastal and estuarine western Atlantic species of anchovy distributed from Suriname to southeastern Brazil.The species is morphologically similar to Anchoviella perfasciata (Poey, 1860) from the Central and western North Atlantic, and it has been suggested in the literature that both are actually synonyms. The recently described Anchoviella sanfranciscana (Barbosa et al., 2017) was reported as endemic to the estuary of the São Francisco River, northeastern Brazil. Most characters proposed as diagnostic for A. sanfranciscana in the description are, however, similar to the ones reported for A. cayennensis and A. perfasciata. To determine the complex taxonomic scenario involving the three species, 24 morphometric and 13 meristic characters of 171 specimens tentatively identified as A. perfasciata (including the holotype) and A. cayennensis from the Central and South Atlantic in addition to the holotype and 19 paratypes of A. sanfranciscana (total: 191 specimens) were analysed. The PCAs of morphometric characters indicate the existence of two groups, which are recognized as A. perfasciata and A. cayennensis, with A. sanfranciscana proposed as a junior synonym of the later. Further evidence from gill arch dentition also indicates that A. perfasciata and A. cayennensis are distinct valid species. A redescription of A. cayennensis is presented, with a neotype proposed for the species. Confirmation of the identity of specimens attributed to A. cayennensis indicates that its southern limit of distribution is in the Rio de Janeiro State, southeastern Brazil. An updated taxonomic key for the estuarine and coastal Atlantic species of Anchoviella is also presented.

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Section: Resultsmentioning

confidence: 99%

“…Localities of specimens of Anchoviella cayennensis identified after the taxonomic revision (white circles: non‐type specimens; black circle: type locality), with additional locality information from Whitehead (1973; red circles) and Hildebrand and de Carvalho (1948; yellow circles)…”

Section: Resultsmentioning

confidence: 99%

Redescription of Anchoviella cayennensis (Puyo, 1945) (Clupeiformes: Engraulidae), with the synonymization of Anchoviella sanfranciscana Barbosa, Gomes da Silva, da Rocha Araújo & Carvalho, 2017 and remarks on Anchoviella perfasciata (Poey, 1860)

Agostinho

Loeb

Dario

2022

Journal of Fish Biology

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“…1.392 (Kingsford et al, 2019) 9.07 (Kavanagh, 2000) 15.3 (Kavanagh, 1996) 0.477 (Kingsford et al, 2019) 0.490 (Froese & Pauly, 2002) 14.0 (Bergstad et al, 2001) 21.0 (Froese & Pauly, 2002) 0.600 (Cook, 2004;ICES, 1998) 0.480 (Froese & Pauly, 2002) 3.69 (Luo, 1991) 11.0 (Hildebrand, 1963) 2.360 (Newberger & Houde, 1995) 0.140 (Froese & Pauly, 2002) 54.00 (Tesch, 1977) 145.0 (Froese & Pauly, 2002) 0.230 (Svedäng, 1999) 1.330 (Tricas, 1986) 7.10 (Tricas, 1986) 9.5 (Tricas, 1986) 0.518 (Goatley & Bellwood, 2016) 0.320 (Froese & Pauly, 2002) 16.70 (Froese & Pauly, 2002) 51.0 (Froese & Pauly, 2002) 0.168 (Beverton, 1963;Cushing, 1959) 1.200 (Froese & Pauly, 2002) 2.50 (Froese & Pauly, 2002) 3.8 (Froese & Pauly, 2002) 1.515 (Weyl & Booth, 1999) 0.120 (Froese & Pauly, 2002) 42.00 (Spitz et (Brandhorst, 1974;Iversen et al, 1993;Schaefer, 1967) 1.700 (Froese & Pauly, 2002) 8.18 (Funamoto et al, 2004) 18.0 (Froese & Pauly, 2002) 0.630 (Iversen et al, 1993) 0.380 (Froese & Pauly, 2002) 13.50 (Richardson, 1980) 24.0…”

Section: Parent-offspring Association Functionmentioning

confidence: 99%

Why we cannot always expect life history strategies to directly inform on sensitivity to environmental change

Rademaker,

van Leeuwen,

Smallegange

2024

Journal of Animal Ecology

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Variation in life history traits in animals and plants can often be structured along major axes of life history strategies. The position of a species along these axes can inform on their sensitivity to environmental change. For example, species with slow life histories are found to be less sensitive in their long‐term population responses to environmental change than species with fast life histories. This provides a tantalizing link between sets of traits and population responses to change, contained in a highly generalizable theoretical framework. Life history strategies are assumed to reflect the outcome of life history tradeoffs that, by their very nature, act at the individual level. Examples include the tradeoff between current and future reproductive success, and allocating energy into growth versus reproduction. But the importance of such tradeoffs in structuring population‐level responses to environmental change remains understudied. We aim to increase our understanding of the link between individual‐level life history tradeoffs and the structuring of life history strategies across species, as well as the underlying links to population responses to environmental change. We find that the classical association between lifehistory strategies and population responses to environmental change breaks down when accounting for individual‐level tradeoffs and energy allocation. Therefore, projecting population responses to environmental change should not be inferred based only on a limited set of species traits. We summarize our perspective and a way forward in a conceptual framework.

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“…In 1948In -1949, the author studied the Brazilian Engraulidae of the genus Anchoviella, under the supervision of the late Dr. Samuel F. Hildebrand, ichthyologist of the U. S. Fish & Wildlife Service, Washington.…”

Section: 'Limentioning

confidence: 99%

Engraulídeos brasileiros do gênero Anchoviella

Carvalho¹

1951

Bol. Inst. Paul. Oceanogr.

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Em trabalho anterior (Carvalho 1950, p. 43), tivemos ocasião de fazer referências à confusão reinante na família Engrau~idae, situação essa, contudo, mais favorável do que a evidenciada por Ihering (1930, p. 2) em relação aoS' Clupeídeos em geral e por Storey (1938, p. 4 Dada a extensão da nossa costa e a ausência de recursós materiais de que nos ressentimos, não será exagerado dizer-se que o estudo dos / '\ nossos Engraulídeos está longe de atingir a sua méta final. Com exceção da região litorân ea do Est. de S" Paulo, onde houve abundante material,

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Notes on Some Brazilian Anchovies (Family Engraulidae) with Descriptions of Four New Species

Cited by 5 publications

References 0 publications

Redescription of Anchoviella cayennensis (Puyo, 1945) (Clupeiformes: Engraulidae), with the synonymization of Anchoviella sanfranciscana Barbosa, Gomes da Silva, da Rocha Araújo & Carvalho, 2017 and remarks on Anchoviella perfasciata (Poey, 1860)

Redescription of Anchoviella cayennensis (Puyo, 1945) (Clupeiformes: Engraulidae), with the synonymization of Anchoviella sanfranciscana Barbosa, Gomes da Silva, da Rocha Araújo & Carvalho, 2017 and remarks on Anchoviella perfasciata (Poey, 1860)

Why we cannot always expect life history strategies to directly inform on sensitivity to environmental change

Engraulídeos brasileiros do gênero Anchoviella

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