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48 results for “Annona”
Figure 7 in Life history patterns of coleopteran pollinators of Annona crassiflora Mart. in the Brazilian Cerrado
Figure 7. Pollinators of Annona crassiflora in a Cerrado area in the municipality of Chapada dos Guimarães, MT. (a) Dorsal habitus of Cyclocephala octopunctata (male). (b) Dorsal habitus of Cyclocephala octopunctata (female). (c) Dorsal habitus of Cyclocephala celata (male). (d) Dorsal habitus of Cyclocephala celata (female).
Figure 6 in Life history patterns of coleopteran pollinators of Annona crassiflora Mart. in the Brazilian Cerrado
Figure 6. Quantitative data on the visitation of Annona crassiflora flowers in a Cerrado area in the municipality of Chapada dos Guimarães, MT. (a) Number of coleopteran and non-coleopteran visitors of anthetic flowers. (b) Number of insect flower visitors sorted by order. (c) Number of beetles visiting anthetic flowers, classified at the family level. (d) Number of beetles visiting anthetic flowers classified at the species and morphospecies levels.
Figure 10 in Life history patterns of coleopteran pollinators of Annona crassiflora Mart. in the Brazilian Cerrado
Figure 10. Quantitative data on the visitation of Annona crassiflora flowers by both Cyclocephala species sampled in this study. (a) Number of individuals of Cyclocephala octopunctata (n = 66) classified according to the anthesis phase of the flowers in which they were found. (b) Number of individuals of Cyclocephala celata (n = 16) classified according to the anthesis phase of the flowers in which they were found. (c) Distribution of the number of individuals of C. octopunctata per sampled flower (n = 41 flowers). (d) Distribution of the number of individuals of C. celata per sampled flower (n = 11 flowers).
Figure 11 in Life history patterns of coleopteran pollinators of Annona crassiflora Mart. in the Brazilian Cerrado
Figure 11. Individuals of Cyclocephalini found in post-anthetic flowers of Annona crassiflora in a Cerrado area in the municipality of Chapada dos Guimarães, MT. (a) A specimen of Cyclocephala celata from a flower found on the ground under the tree crown in the morning after anthesis. Note the pollen tetrads adhered to the tibial and tarsal setae of the right mesothoracic leg. (b) Individuals of C. octopunctata collected in the morning after anthesis from a flower still attached to the pedicel.
Figure 9 in Life history patterns of coleopteran pollinators of Annona crassiflora Mart. in the Brazilian Cerrado
Figure 9. Cyclocephala celata visiting flowers of Annona crassiflora in a Cerrado area in the municipality of Chapada dos Guimarães, MT. (a) Here, the elytra (arrow) of one individual of C. celata are visible inside a female-phase flower. (b) Individuals of C. celata covered in pollen exiting a male-phase flower. (c) Two individuals of C. celata covered in pollen inside a recently fallen corolla that was picked from the ground beneath an A. crassiflora tree. Note that their heads are directed towards the base of the petals, where the nutritious basal lobes are located. (d) This individual of C. celata had just escaped from inside a corolla that was found on the ground under an A. crassiflora individual on the day following flower anthesis.
Figure 3 in Life history patterns of coleopteran pollinators of Annona crassiflora Mart. in the Brazilian Cerrado
Figure 3. Some steps in the floral cycle of Annona crassiflora in a Cerrado area in the municipality of Chapada dos Guimarães, MT. (a) Developing flower buds photographed in early August, almost two months before the flowering season of A. crassiflora. (b) Open flower chamber photographed in the morning before the onset of anthesis. (c) Flower entering the female phase, photographed from below during crepuscule. Note the sticky, transparent, glossy substance on the gynoecium (the stigmatic exudate; arrow). Petals were spread open to show internal structures.
Figure 2 in Life history patterns of coleopteran pollinators of Annona crassiflora Mart. in the Brazilian Cerrado
Figure 2. Study area located in the Cerrado of the municipality of Chapada dos Guimarães, MT, with the positions of the 24 individuals of Annona crassiflora analysed in this research (red circles). Source: Google Earth.
FIGURE 1 in Redetermination of host plants reveals that the rust fungi Aecidium annonae, Aecidium chrysophaeum and Cerotelium xylopiae occur on Diospyros species (Ebenaceae) instead of Annonaceae
FIGURE 1. Micromorphological characteristics distinguishing Ebenaceae and Annonaceae: a. Diospyros sericea, surface of trichome tip covered with elongated spindle shaped warts; b. Annona holosericea Saff., section through leaf showing two globular secretory cells.
FIGURE 2 in Redetermination of host plants reveals that the rust fungi Aecidium annonae, Aecidium chrysophaeum and Cerotelium xylopiae occur on Diospyros species (Ebenaceae) instead of Annonaceae
FIGURE 2. Aecidium annonae: a. Infected leaves of Diospyros hispida (holotype). b–d. Aecia: b. peridial cells in longitudinal section (inner side on the left); c. inner side of peridial cells in face view; d. aeciospores in face view and optical sections.
FIGURE 3 in Redetermination of host plants reveals that the rust fungi Aecidium annonae, Aecidium chrysophaeum and Cerotelium xylopiae occur on Diospyros species (Ebenaceae) instead of Annonaceae
FIGURE 3. Aecidium chrysophaeum: a. Infected leaves of Diospyros artanthifolia (lectotype). c. Subepidermal spermogonium in section. c–f. Aecia: c. aecium in section; d. aeciospores with enlarged distal wall, insert shows single spore with lumen stained by cottonblue; e. inner side of peridial cells in face view; f. outer side of peridial cells in face view and optical section.
FIGURE 4 in Redetermination of host plants reveals that the rust fungi Aecidium annonae, Aecidium chrysophaeum and Cerotelium xylopiae occur on Diospyros species (Ebenaceae) instead of Annonaceae
FIGURE 4. Cerothelium diospyri: a–b. Comparison of size and shape between leaves of a. Xylopia sericea A. St.-Hill. (Annonaceae) infected by Dasyspora winteri (Pazschke) Beenken and b. Diospyros sericea (Ebenaceae) infected by Cerothelium diospyri. Upper leaf side is shown on the left and lower side is shown on the right. c–f. Telia of Cerotelium diospyri on Diospyros sericea (holotype); c. Telium breaking through the papillate leaf epidermis, in section; d. teliospores in gelatinous matrix; e. germinating teliospore; f. drawings of two teliospores germinating with basidia, with two of the six basidiospores germinating.
FIGURE 3. A. M in First record of Monalonion velezangeli (Hemiptera: Miridae) affecting avocado and cherimoya (Annona cherimola) as new hosts in Ecuador
FIGURE 3. A. M. velezangeli adult in vivo. B. Antennae with four segments. C. Rostrum of M. velezangeli with its four segments. D and E. Coloration diversity in the M. velezangeli pronotum (P), scutellum (S). F and G. Coloration diversity in the legs of M. velezangeli and creamy white strip in the middle of the femurs (CWS). H and I. Coloration diversity in forewings in cuneus (Cu) and corium (Co), spots inside (Si) and outside the vein in the membrane (Me).
FIGURE 1. A in First record of Monalonion velezangeli (Hemiptera: Miridae) affecting avocado and cherimoya (Annona cherimola) as new hosts in Ecuador
FIGURE 1. A. Nymph of M. velezangeli on an avocado plant. B. Adult of M. velezangeli on an avocado fruit. C. M. velezangeli bites on young avocado branches. D. Damage to small fruit of 2.2 and 2.4 cm in polar diameter.
FIGURE 4 in First record of Monalonion velezangeli (Hemiptera: Miridae) affecting avocado and cherimoya (Annona cherimola) as new hosts in Ecuador
FIGURE 4. Structures of the male genitalia of M. velezangeli. A. Aedeagus: teak opening (at), teak (te), endosoma (en), seminal duct (sd), phallus base (bp), captured process. B. Left paramere: basal region (br), paramere body (pb), apical region (ar). C. Right paramere: basal region (br), paramere body (pb), apical region (ar). D. Agarose gel with PCR products for the COI fragment of five of the collected samples (MM= molecular weight marker, CN = negative control).
FIGURE 2. Confirmation test for M in First record of Monalonion velezangeli (Hemiptera: Miridae) affecting avocado and cherimoya (Annona cherimola) as new hosts in Ecuador
FIGURE 2. Confirmation test for M. velezangeli damage in avocado and cherimoya. A. Healthy fruit. B. Fruit confined with an adult M. velezangeli. C. Fruit of 6.3 cm in polar diameter with damage due to the bug's puncture. D. Fruit confined with an adult M. velezangeli. E. Fruit affected by M. velezangeli. F. Fruit with recent pitting (left) and fruit with old pitting (right) and beginnings of a saprophytic fungal infection.
Data from: A Mesoamerican origin of cherimoya (Annona cherimola Mill.). Implications for the conservation of plant genetic resources
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Data from: Climatic drivers of leaf traits and genetic divergence in the tree Annona crassiflora: a broad spatial survey in the Brazilian savannas
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Figure 5 in The inhibitory and anticancer properties of Annona squamosa L. seed extracts
Figure 5. (A) XRD spectra of A. squamosa presentation projecting extract image. (B) ESE of A. squamosa powder measured by energy dispersive X-ray spectroscopy (C) ESE of A. squamosa powder as seen using scanning electron microscopy.
Figura 1 in Un nuevo registro de Optatus palmaris Pascoe (Coleoptera: Curculionidae) asociado con Annona L. (Annonaceae) en el Estado de México, México
Figura 1. Optatus palmaris Pascoe dañando frutos de anonáceas. A. O. palmaris en vista lateral, B. Adulto perforando frutos de A. cherimola Mill., C. Adultos de O. palmaris alimentándose de A. diversifolia Saf., D. Larvas alimentándose de chirimoya.
Annona squamosa Leaf Extract Inhibit Migration of Human Cervical Cancer Cells Through MMP-9 Expression
<p><strong>Table 1. Interpretation of suspected acetogenin compounds isolates</strong></p>
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