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Figure 3 in Feeding habits of Scorpaena notata (Scorpaenidae) from eastern Adriatic Sea
Figure 3. – Composition of Scorpaena notata diet among size-classes, based on the %IRI values of the major prey groups.
FIGURE 2 in Feeding habits of the cockfish, Callorhinchus callorynchus (Holocephali: Callorhinchidae) from off northern Argentina
FIGURE 2 | Length-frequency distributions of Callorhinchus callorynchus for females (F) and males (M) off northern Argentina.
FIGURE 4 in Feeding habits of the cockfish, Callorhinchus callorynchus (Holocephali: Callorhinchidae) from off northern Argentina
FIGURE 4 | Changes in consumption of isopods, amphipods, gastropods and anomuran crabs with body size, season and region of Callorhinchus callorynchus females estimated by generalized linear models. In gastropods: cold season with dashed lines and open circles; warm season with solid lines and solid circles. In anomuran crabs: north region with dashed lines and open circles; center region with solid lines and solid circles.
Figure 5 in Seasonal analysis of food items and feeding habits of endangered riverine catfish Rita rita (Hamilton, 1822)
Figure 5. Links between the fish size groups based on cluster analysis in R. rita sampled from Padma River (Roman numbers indicated the different size group of fish, such as I = 9-14 cm, II =>14-19 cm, III =>19-24 cm, IV =>24-29 cm and V =>29-34 cm).
Figures 1-4 from: Gottlieb Almeida AP, Zardo EL, Toni C, Behr ER, Picolli da Silva L, Vieira JP, Loro VL, Baldisserotto B (2018) Composition of gastrointestinal content, protease and lipase activities in summer and winter of four freshwater siluriforms (Teleostei: Actinopterygii) with two different feeding habits. Zoologia 35: 1-8. https://doi.org/10.3897/zoologia.35.e13286
Figures 1-4 Species used in the analysis: (1) Rhamdia quelen; (2) Pimelodus maculatus; (3) Loricariichthys anus; (4) Hypostomus commersoni. Figures 1, 2 and 4 kindly provided by Alexssandro G. Becker and figure 3 by Luiz R. Malabarba.
Figures 10-11 from: Gottlieb Almeida AP, Zardo EL, Toni C, Behr ER, Picolli da Silva L, Vieira JP, Loro VL, Baldisserotto B (2018) Composition of gastrointestinal content, protease and lipase activities in summer and winter of four freshwater siluriforms (Teleostei: Actinopterygii) with two different feeding habits. Zoologia 35: 1-8. https://doi.org/10.3897/zoologia.35.e13286
Figures 10-11 Lipase activity in the omnivorous R. quelen and P. maculatus and detritivorous L. anus and H. commersoni in the summer and winter: (10) anterior intestine; (11) posterior intestine. Different letters indicate significant differences between species in the same season. * Indicates a significant difference from the summer in the same segment (p < 0.05). (U, a Caraway unit) (n = 15 from each species at each season).
Figures 5-9 from: Gottlieb Almeida AP, Zardo EL, Toni C, Behr ER, Picolli da Silva L, Vieira JP, Loro VL, Baldisserotto B (2018) Composition of gastrointestinal content, protease and lipase activities in summer and winter of four freshwater siluriforms (Teleostei: Actinopterygii) with two different feeding habits. Zoologia 35: 1-8. https://doi.org/10.3897/zoologia.35.e13286
Figures 5-9 Proteolytic enzymatic activities in the omnivorous R. quelen and P. maculatus and detritivorous L. anus and H. commersoni in the summer and winter: (5) pepsin in the stomach; (6) trypsin in the anterior intestine; (7) trypsin in the posterior intestine; (8) chymotrypsin in the anterior intestine; (9) chymotrypsin in the posterior intestine. Different letters indicate significant differences between species in the same season. * Indicates a significant difference from summer in the same segment (p < 0.05). (U, a Caraway unit) (n = 15 from each species at each season).
Figures 11-12 from: Lameiro FR, Condini MV, Brito CP, Vieira JP (2018) The feeding habits of the endemic Remo flounder, Oncopterus darwinii (Actinopterygii: Pleuronectidae), in an exposed sandy beach's surf zone in southern Brazil. Zoologia 35: 1-8. https://doi.org/10.3897/zoologia.35.e15038
Figures 11-12 Feeding strategy diagram for individuals of Oncopterus darwinii caught at both sites: (11) Cassino; (12) Mar Grosso). The prey-specific abundance plotted against the frequency of occurrence of food items for O. darwinii.
Figures 7-10 from: Lameiro FR, Condini MV, Brito CP, Vieira JP (2018) The feeding habits of the endemic Remo flounder, Oncopterus darwinii (Actinopterygii: Pleuronectidae), in an exposed sandy beach's surf zone in southern Brazil. Zoologia 35: 1-8. https://doi.org/10.3897/zoologia.35.e15038
Figures 7-10 Average values (± SD) of prey number and volume in the stomach contents of Oncopterus darwinii at Cassino (7–8) and Mar Grosso (9–10), respectively. The data are summarized for three size classes (<60 mm TL, 60–100 mm TL, and >100 mm TL), and shared letters above each box indicate non-significant differences among the size classes.
Figures 3-6 from: Lameiro FR, Condini MV, Brito CP, Vieira JP (2018) The feeding habits of the endemic Remo flounder, Oncopterus darwinii (Actinopterygii: Pleuronectidae), in an exposed sandy beach's surf zone in southern Brazil. Zoologia 35: 1-8. https://doi.org/10.3897/zoologia.35.e15038
Figures 3-6 Average values (± SD) of prey number and volume in the stomach contents of Oncopterus darwinii at Cassino (3–4) and Mar Grosso (5–6), respectively. The data are summarized for three seasons (winter, spring and summer) and shared letters above each box indicate non-significant differences among the seasons.
Figure 2 from: Lameiro FR, Condini MV, Brito CP, Vieira JP (2018) The feeding habits of the endemic Remo flounder, Oncopterus darwinii (Actinopterygii: Pleuronectidae), in an exposed sandy beach's surf zone in southern Brazil. Zoologia 35: 1-8. https://doi.org/10.3897/zoologia.35.e15038
Figure 2 Number of Oncopterus darwinii juveniles caught at Cassino (black bars) and Mar Grosso (grey bars) between August 2009 and July 2010.
Fig. 2 in Feeding habits and habitat of herbivorous mammals from the Early-Late Hemphillian (Miocene) of Costa Rica
Fig. 2. Stratigraphic column of the fossil-bearing locality, San Gerardo de Limoncito, modified from Laurito and Valerio (2010). Abbreviations: C, clay; c, coarse sandstone; Co, conglomerate; f, fine; g, gravel; m, middle; u., unconformity.
Fig. 1 in Temporal and ontogenetic variations in feeding habits of Hollandichthys multifasciatus (Teleostei: Characidae) in coastal Atlantic rainforest streams, southern Brazil
Fig. 1. Northern coast of Santa Catarina State (southern Brazil), showing the city of São Francisco do Sul and the location of the study sites (1, 2).
FIGURES 3 in Description of the larva of Macrostemum floridum (Navás 1929) (Trichoptera Hydropsychidae) and its feeding habits in Kaengkrung National Park, southern Thailand.
FIGURES 3.Larva of Macrostemum floridum (Navás 1929). 3, labrum, dorsal.
Data from: Utility of geometric morphometrics for inferring feeding habit from mouthpart morphology in insects: tests with larval Carabidae (Insecta: Coleoptera)
Feeding habits are important life-history traits in animals; however, methods for their determination are not well established in many species. The larvae of the beetle family Carabidae are an example. The present study tested the utility of geometric morphometrics of mouthpart morphology to infer the feeding habits of carabid larvae. Using Pterostichus thunbergi as a model system, larval feeding habits were inferred using geometric morphometrics of mouthparts and the results were compared with those obtained from rearing experiments. The rearing experiments indicated that P. thunbergi larvae are carnivores that require snails as an essential part of the diet. Through geometric morphometrics, associations between mouthpart morphology and larval feeding habits were confirmed for species in which these two traits are known. A discriminant analysis using these associations classified P. thunbergi larvae as snail/slug feeders, which is a result compatible with the rearing experiments. Geometric morphometrics also revealed that morphological integration and ontogenetic shape change might play roles in the diversification of mouthpart morphology. Overall, these results demonstrate the utility of the geometric morphometrics of mouthparts to infer feeding habit and to clarify the mechanisms of mouthpart morphological diversification in the study group, and the results also serve as a basis for future studies of other insect groups.
Figure 2 in Feeding habits of Scorpaena notata (Scorpaenidae) from eastern Adriatic Sea
Figure 2. – Length-frequency distribution of Scorpaena notata caught in the eastern Adriatic Sea.
Figure 3 in Feeding habit of Brown trout (Salmo trutta fario) in upper parts of river Swat, Pakistan
Figure 3. Relationship between feeding intensity and length groups.
Figure 1 from: Lameiro FR, Condini MV, Brito CP, Vieira JP (2018) The feeding habits of the endemic Remo flounder, Oncopterus darwinii (Actinopterygii: Pleuronectidae), in an exposed sandy beach's surf zone in southern Brazil. Zoologia 35: 1-8. https://doi.org/10.3897/zoologia.35.e15038
Figure 1 Location of the six sampling sites in the coastline of Rio Grande do Sul, Brazil.
Controlling ECC and Terminating Bottle-feeding Habits Among Toddlers Using a Modified Oral Care Package
ClinicalTrials.gov study NCT04440137. IPD Sharing: NO. Countries: 1. Publications: 0.
Data from: Utility of geometric morphometrics for inferring feeding habit from mouthpart morphology in insects: tests with larval Carabidae (Insecta: Coleoptera)
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