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Figure 8 in The feeding strategy of the predatory Gyrineum natator (Gastropoda: Neotaenioglossa: Ranellidae) in the Cape d'Aguilar Marine Reserve, Hong Kong, with a review of sulphuric acid use in prey access by the Tonnoidea and experimentally derived estimates of consumption
Figure 8. Gyrineum natator. Phase-contrast micrographs of the salivary glands of three individuals following treatment with barium chloride for 50 minutes. (A–C) Three untreated controls; (D–F) three treated individuals.
Figure 2 in The feeding strategy of the predatory Gyrineum natator (Gastropoda: Neotaenioglossa: Ranellidae) in the Cape d'Aguilar Marine Reserve, Hong Kong, with a review of sulphuric acid use in prey access by the Tonnoidea and experimentally derived estimates of consumption
Figure 2. Gyrineum natator. The holes made in four shells (A–D) of Saccostrea mordax by individuals held in experimental aquaria. Only A shows a near-circular access hole, but other irregular ones (B–D) appear to have been created by acid attack as there would be no need for the radula alone to make such large holes.
Figure 4 in The feeding strategy of the predatory Gyrineum natator (Gastropoda: Neotaenioglossa: Ranellidae) in the Cape d'Aguilar Marine Reserve, Hong Kong, with a review of sulphuric acid use in prey access by the Tonnoidea and experimentally derived estimates of consumption
Figure 4. Gyrineum natator. The relationship between shell height (in mm) and wet tissue weights [Log(W + 1) (in grams)] of seven individuals including the two experimental animals with shell heights of 34.6 and 33.6 mm.
Figure 5 in The feeding strategy of the predatory Gyrineum natator (Gastropoda: Neotaenioglossa: Ranellidae) in the Cape d'Aguilar Marine Reserve, Hong Kong, with a review of sulphuric acid use in prey access by the Tonnoidea and experimentally derived estimates of consumption
Figure 5. Gyrineum natator. The accumulated % wet tissue weights of oyster tissues consumed by the two approximately equal-sized individuals of G. natator held in filtered and unfiltered seawater aquaria.
Figure 1 in The feeding strategy of the predatory Gyrineum natator (Gastropoda: Neotaenioglossa: Ranellidae) in the Cape d'Aguilar Marine Reserve, Hong Kong, with a review of sulphuric acid use in prey access by the Tonnoidea and experimentally derived estimates of consumption
Figure 1. Gyrineum natator. The living animal as seen from the ventral aspect crawling on an upturned sheet of glass immersed in seawater, and showing the extended proboscis.
Figure 7 in The feeding strategy of the predatory Gyrineum natator (Gastropoda: Neotaenioglossa: Ranellidae) in the Cape d'Aguilar Marine Reserve, Hong Kong, with a review of sulphuric acid use in prey access by the Tonnoidea and experimentally derived estimates of consumption
Figure 7. Gyrineum natator. (A) A transverse section through one of the paired salivary glands and the associated pharyngeal (oesophageal) gland; (B) developing salivary gland tubules at the outer edge of the salivary gland; (C) fully developed sulphuric acid producing salivary gland cells; (D) a transverse section through a pharyngeal (oesophageal) gland tubule; (E) a transverse section through the salivary gland/pharyngeal gland duct.
Figure 3 in The feeding strategy of the predatory Gyrineum natator (Gastropoda: Neotaenioglossa: Ranellidae) in the Cape d'Aguilar Marine Reserve, Hong Kong, with a review of sulphuric acid use in prey access by the Tonnoidea and experimentally derived estimates of consumption
Figure 3. Saccostrea mordax. The relationship between total weight [Log(TotW + 1) (in grams)] and wet tissue weights [Log(W + 1) (in grams)] of the 34 oyster individuals.
Figure 9 in The feeding strategy of the predatory Gyrineum natator (Gastropoda: Neotaenioglossa: Ranellidae) in the Cape d'Aguilar Marine Reserve, Hong Kong, with a review of sulphuric acid use in prey access by the Tonnoidea and experimentally derived estimates of consumption
Figure 9. Gyrineum natator. Phase-contrast micrographs of (A) the salivary gland and (B) the pharyngeal (oesophageal) gland after treatment with barium chloride for 50 minutes.
Figure 6 in The feeding strategy of the predatory Gyrineum natator (Gastropoda: Neotaenioglossa: Ranellidae) in the Cape d'Aguilar Marine Reserve, Hong Kong, with a review of sulphuric acid use in prey access by the Tonnoidea and experimentally derived estimates of consumption
Figure 6. Gyrineum natator. The foregut anatomy, as seen from the dorsal aspect, and showing the hypertrophied and paired salivary glands and the single pharyngeal (oesophageal) gland. Redrawn after Taylor (1998).
Data from: A multiple peak adaptive landscape based on feeding strategies and roosting ecology shaped the evolution of cranial covariance structure and morphological differentiation in phyllostomid bats
We explored the evolution of morphological integration in the most noteworthy example of adaptive radiation in mammals, the New World leaf-nosed bats, using a massive dataset and by combining phylogenetic comparative methods and quantitative genetic approaches. We demonstrated that the phenotypic covariance structure remained conserved on a broader phylogenetic scale but also showed a substantial divergence between inter-clade comparisons. Most of the phylogenetic structure in the integration space can be explained by splits at the beginning of the diversification of major clades. Our results provide evidence for a multiple peak adaptive landscape in the evolution of cranial covariance structure and morphological differentiation, based upon diet and roosting ecology. In this scenario, the successful radiation of phyllostomid bats was triggered by the diversification of dietary and roosting strategies, and the invasion of these new adaptive zones lead to changes in phenotypic covariance structure and average morphology. Our results suggest that intense natural selection preceded the invasion of these new adaptive zones and played a fundamental role in shaping cranial covariance structure and morphological differentiation in this hyper-diverse clade of mammals. Finally, our study demonstrates the power of combining comparative methods and quantitative genetic approaches when investigating the evolution of complex morphologies.
Data from: A multiple peak adaptive landscape based on feeding strategies and roosting ecology shaped the evolution of cranial covariance structure and morphological differentiation in phyllostomid bats
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Data from: Multichannel feeding by spider functional groups is driven by feeding strategies and resource availability
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Feeding Mom Feeding Infant's Microbiota: Nutritional Strategies for Improving Breast Milk Composition and Infant Health
ClinicalTrials.gov study NCT05259059. IPD Sharing: Not stated. Countries: 1. Publications: 0.
Protein in Feeding Strategies to Accelerate Muscle Recovery From ACL Reconstruction
ClinicalTrials.gov study NCT03492021. IPD Sharing: Not stated. Countries: 1. Publications: 0.
Appropriate Complmentary Feeding Strategies in Infants
ClinicalTrials.gov study NCT01412411. IPD Sharing: Not stated. Countries: 1. Publications: 0.
Multisite Feeding Study: Home Surveillance and Feeding Strategies in Infants With Complex Single Ventricle
ClinicalTrials.gov study NCT00257517. IPD Sharing: Not stated. Countries: 1. Publications: 0.
Data from: Gizzard vs. teeth, it’s a tie: food-processing efficiency in herbivorous birds and mammals and implications for dinosaur feeding strategies
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Genome wide transcriptome analysis provides bases on colonic mucosal immune system development in neonatal calves affected by colostrum feeding strategies in neonatal calves
GEO Series GSE113264. Bos taurus. 27 samples. Type: Expression profiling by high throughput sequencing.
Strategies towards improved feed efficiency in pigs comprise molecular shifts in hepatic lipid and carbohydrate metabolism
GEO Series GSE95223. Sus scrofa. 12 samples. Type: Expression profiling by array.
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International Brain Laboratory public data
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OpenNeuro
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