Feeding in the Fairy Shrimp Streptocephalus proboscideus (Frauenfeld) (Branchiopoda: Anostraca). I. Aspects of the Feeding Biology

1993 ◽  
Vol 13 (2) ◽  
pp. 235 ◽  
Author(s):  
Luc Brendonck
Keyword(s):  
Biology ◽  
2021 ◽  
Vol 10 (8) ◽  
pp. 695
Author(s):  
Sara Farhadi ◽  
Behrooz Atashbar Kangarloei ◽  
Ahmad Imani ◽  
Kourosh Sarvi Moghanlou

B. orientalis, fairy shrimp, is often among the most conspicuous invertebrates inhabiting temporary aquatic habitats with a typical variation in environmental conditions. Its life history characteristics and biochemical composition were studied under four different photoperiodic regimes (24L:0D, 0L:24D, 16L:8D, and 12L:12D). The significantly highest cumulative and initial hatching rates (48 h) were obtained at 24L:0D (p < 0.05). Cultivating the larvae under different photoperiods did not significantly affect specific growth rate (SGR) (p > 0.05). However, higher final total body length and daily growth rate were recorded under constant darkness. Higher lipid content was found at 24L:0D to the extent that it was more than two times higher than that at 16L:8D and 12L:12D (p < 0.05). There was also a remarkable increase in body crude protein content at 24L:0D (p < 0.05). Body fatty-acid profiles of the fairy shrimps were also affected by culture condition (p < 0.05). Extension of lighting period resulted in a subtle increase in body contents of arginine, lysine, histidine, isoleucine, leucine, valine, methionine, and phenylalanine, especially in the group kept under a 16L:8D regime. The highest and lowest digestive enzyme activity was observed at 0L:24D and 24L:0D, respectively (p < 0.05). In contrast, the highest and lowest soluble protein content was recorded at 24L:0D and 0L:24D, respectively (p < 0.05). Similarly, antioxidant status was significantly higher at 0L:24D (p < 0.05). In conclusion, a 16L:8D light–dark cycle might be an optimal condition in terms of growth performance and physio-biochemical characteristics. These findings could be helpful in optimizing the rearing conditions for upscaling B. orientalis production.


2021 ◽  
Author(s):  
Regina Lopes da Cunha ◽  
Jordi Sala ◽  
Margarida Machado ◽  
Dani Boix ◽  
Celine Madeira ◽  
...  

2008 ◽  
Vol 28 (3) ◽  
pp. 543-550 ◽  
Author(s):  
D. Christopher Rogers ◽  
Oscar Zúñiga ◽  
Patricio De los Ríos
Keyword(s):  

2020 ◽  
Vol 248 (3302) ◽  
pp. 17
Author(s):  
Jake Buehler
Keyword(s):  

2017 ◽  
Vol 57 (20) ◽  
pp. 265 ◽  
Author(s):  
Caio José Carlos ◽  
Jéssica Guimarães Alvarenga ◽  
Mariana Scain Mazzochi

In this paper, we describe the skulls of Magnificent Frigatebird Fregata magnificens (Fregatidae) and Brown Booby (Sulidae) Sula leucogaster, with focus on the structures associated with the Musculi mandibulae. We discuss the results in the context of the feeding biology of the two species, which feed mainly on flying fish and squids. Frigatebirds capture prey from just above, or just below, the water surface in flight. The hook-shaped Apex maxillae in F. magnificens can be viewed as an adaptation for grasping prey from near the water surface. Boobies catch prey by plunging; thus, the dorsoventrally flattened skull and conical bill of S. leucogaster may reduce water resistance when it dives, or swims underwater. The bill is long in both species, such that it is on average 70% of the whole skull length in F. magnificens and 60% in S. leucogaster. Consequently, the Mm. mandibulae in the two species are more posteriorly positioned relative to the Apex rostri. This results in low mechanical advantage for the mandible opening-closing lever, indicating adaptations for a fast, rather than a strong, bite. Fast-moving mandibles would be advantageous for ‘mandibulating’ prey while swallowing. The Fossa musculorum temporalium and the Palatum osseum in both species provide a broad area for origins of the Musculus adductor mandibulae externus (all parts) and the Musculus pterygoideus. The Processus orbitalis quadrati is longer and thicker in F. magnificens than in S. leucogaster, and so is the Musculus pseudotemporalis profundus. We suggest that Mm. adductores mandibulae are relatively well developed in the two species; therefore, their mandibulae are still probably capable of a powerful adduction. In both species there is a mechanisms that contribute to protect the jaws from disarticulation and damage. Such mechanism involves the incorporation of a ‘flange-like’ Crista intercotylare on the Margo medialis cotylae medialis fossae articularis quadratica that grips the Condylus medialis quadrati. In S. leucogaster, the retractor-stop ‘notch’ formed by Ossa lacrimale et nasale also serves to protect the jaws against sudden external forces when birds are diving or swimming underwater for prey. A more detailed hypothesis for the jaw movements and strength in F. magnificens and in S. leucogaster and their relation with feeding habits should necessarily incorporate data on the jaw and anterior neck musculatures.


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