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211 results for “Feeding habits”
Figure 1 in Review of sterlet (Acipenser ruthenus L. 1758) (Actinopterygii: Acipenseridae) feeding habits in the River Danube, 1694-852 river km
Figure 1. Map with nine locations along the River Danube (1694–852 river km) where sterlet diet was analysed.
Figs 50–53 in Morphology of the larvae and biology of the adults of Psilorrhynchus bifasciatus do not confirm previous hypotheses about systematics and feeding habits (Coleoptera: Cantharidae)
Figs 50–53. Habitus of fixed and live Psilorrhynchus specimens. 50–51 – museum specimens of P. bifasciatus (Blanchard) (50) and P. abdominalis (Perty) (51) as presented in the genus revision (Bංൿൿං 2017a) showing a pale-yellow elytral background colouration. 52–53 – live specimens of P. abdominalis from Rio de Janeiro state, showing an intense reddish elytral colouration. Figs 50 and 51 adapted from Bංൿൿං (2017a); 52 by Diogo Luiz (available at inaturalist.org/observations/31961589); 53 by Eric Freitas de Abreu (available at inaturalist.org/observations/56266908).
Figs 39–49 in Morphology of the larvae and biology of the adults of Psilorrhynchus bifasciatus do not confirm previous hypotheses about systematics and feeding habits (Coleoptera: Cantharidae)
Figs 39–49. Morphology of Psilorrhynchus bifasciatus (Blanchard, 1844), second and first instar larvae. 39 – head, second instar; 40 – nasale, second instar; 41–49 – first instar; 41 – head; 42 – nasale; 43–44 – antenna (ventral, dorsal views); 45 – maxillo-labial complex; 46 – foreleg; 47–48 – pretarsus (lateral, ventral views); 49 – apex of abdomen (dorsal view). Scale bars = 0.05 mm, except 39, 41, 46, 49 = 0.1 mm.
Figs 36–38 in Morphology of the larvae and biology of the adults of Psilorrhynchus bifasciatus do not confirm previous hypotheses about systematics and feeding habits (Coleoptera: Cantharidae)
Figs 36–38. Morphology of Psilorrhynchus bifasciatus (Blanchard, 1844), second instar larva (dorsal, ventral, lateral views). Scale bar = 0.5 mm.
Figs 19–35 in Morphology of the larvae and biology of the adults of Psilorrhynchus bifasciatus do not confirm previous hypotheses about systematics and feeding habits (Coleoptera: Cantharidae)
Figs 19–35. Morphology of Psilorrhynchus bifasciatus (Blanchard, 1844), third instar larva. 19 – head, dorsal view; 20 – nasale; 21–22 – antenna (dorsal and ventral views); 23–24 – third antennomere (ventral and dorsal views); 25–26 – mandibula (dorsal and ventral views); 27 – maxillo-labial complex; 28 – hypopharynx; 29 – maxillary palp (dorsal view); 30 – third maxillary papomere (ventral view); 31–32 – second labial palpomere (ventral and dorsal views); 33 – mesothoracic spiracle; 34 – foreleg; 35 – pretarsus. Scale bars = 0.1 mm, except 29 = 0.05 mm, 33 = 0.5 mm, and 34 = 0.5 mm.
Figs 14–18 in Morphology of the larvae and biology of the adults of Psilorrhynchus bifasciatus do not confirm previous hypotheses about systematics and feeding habits (Coleoptera: Cantharidae)
Figs 14–18. Morphology of Psilorrhynchus bifasciatus (Blanchard, 1844), third instar larva. 14 – head and pronotum in dorsal view; 15 – head, ventral view; 16 – head in lateral view; 17–18 – abdominal segments VIII–X in dorsal (17) and ventral views (18). Scale bars = 0.5 mm.
Figs 6–9 in Morphology of the larvae and biology of the adults of Psilorrhynchus bifasciatus do not confirm previous hypotheses about systematics and feeding habits (Coleoptera: Cantharidae)
Figs 6–9. Eggs and larvae of Psilorrhynchus bifasciatus (Blanchard, 1844), 6–7 – eggs pile laid on the soil; 8–9 – first instar larvae hatching.
Figs 1–5 in Morphology of the larvae and biology of the adults of Psilorrhynchus bifasciatus do not confirm previous hypotheses about systematics and feeding habits (Coleoptera: Cantharidae)
Figs 1–5. Live adults of Psilorrhynchus bifasciatus (Blanchard, 1844). 1–2 – habitus of female; 3–5 – specimens in copula and foraging on Matayba guianensis Aubl. (Sapindaceae) in Selvíria, MS, Brazil.
Figs 10–13 in Morphology of the larvae and biology of the adults of Psilorrhynchus bifasciatus do not confirm previous hypotheses about systematics and feeding habits (Coleoptera: Cantharidae)
Figs 10–13. Psilorrhynchus bifasciatus (Blanchard, 1844), third instar larva in dorsal (10), lateral (11), ventral (12) and dorso-lateral views (13). Specimen stained in iodine. Scale bar = 1.0 mm.
Fig. 2 in Feeding Habits Of Sympatric Mustelids In An Agricultural Area Of Hungary
Fig. 2. Changes in biomass of small mammals in the Ormánság region (SW Hungary). Biomass of small mammals was calculated from summarized capture data (from individual weights and MNA)
Fig. 1 in Feeding Habits Of Sympatric Mustelids In An Agricultural Area Of Hungary
Fig. 1. Seasonal diet composition changes of the badger (Meles meles) and the marten (Martes sp.) in the Ormánság region (SW Hungary). W = winter, S = spring, Su = summer, A = autumn, (n) = num-
Figure 4 in Feeding habits of Scorpaena notata (Scorpaenidae) from eastern Adriatic Sea
Figure 4. – Diet composition of Scorpaena notata throughout the year, based on the %IRI values of the major prey groups.
Figure 1 in Feeding habits of Scorpaena notata (Scorpaenidae) from eastern Adriatic Sea
Figure 1. – Study area and sampling sites of Scorpaena notata in the eastern Adriatic Sea. A: Kvarner Archipelago; B: Near Dugi Island; C: Near Šolta Island; D: Near Hvar Island. All sampling sites supported biocoenosis on coastal terrigenous sediments.
Figure 5 in Feeding habits of Scorpaena notata (Scorpaenidae) from eastern Adriatic Sea
Figure 5. – Dendrogram for hierarchical clustering of the prey composition of Scorpaena notata according to sampling sites, using group-average linking of Bray-Curtis similarities calculated on standardized and double root-transformed data of prey abundance. A: Kvarner Archipelago (n = 177); B: Near Dugi Island (n = 220); C: Near Šolta Island (n = 190); D: Near Hvar Island (n = 211).
FIGURE 6 in Feeding habits of the cockfish, Callorhinchus callorynchus (Holocephali: Callorhinchidae) from off northern Argentina
FIGURE 6 | Relationship between valve width (VW) of bivalves and precaudal lenght of Callorhinchus callorynchus. The solid, dashed and dotted lines are 5%, 50% and 95% quantile regressions, respectively.
FIGURE 5 in Feeding habits of the cockfish, Callorhinchus callorynchus (Holocephali: Callorhinchidae) from off northern Argentina
FIGURE 5 | Changes in consumption of bivalves, cumaceans and brachyuran crabs with region, season and maturity stage of Callorhinchus callorynchus females estimated by generalized linear models.
FIGURE 3 in Feeding habits of the cockfish, Callorhinchus callorynchus (Holocephali: Callorhinchidae) from off northern Argentina
FIGURE 3 | Cumulative prey curves as a function of sample size of Callorhinchus callorynchus for total individuals, males and for each group of females considered in the dietary analisis. Mean (continuous lines) ± SD (dashed lines) are plotted.
FIGURE 1 in Feeding habits of the cockfish, Callorhinchus callorynchus (Holocephali: Callorhinchidae) from off northern Argentina
FIGURE 1 | Study area showing where individuals of Callorhinchus callorynchus were captured off northern Argentina. The rectangle in the inset shows the location of the study area in South America.
Figure 3 in Seasonal analysis of food items and feeding habits of endangered riverine catfish Rita rita (Hamilton, 1822)
Figure 3. Seasonal variation in frequency of food items assessed by non-metric multidimensional scaling (nMDS) analysis in R. rita sampled from Padma River.
Figure 2 in Seasonal analysis of food items and feeding habits of endangered riverine catfish Rita rita (Hamilton, 1822)
Figure 2. Fullness index of fish stomach in different seasons (a) and size groups (b) of R. rita sampled from Padma River.
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