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308 results for “bromeliads”
FIGURES 20–25. Acentroptera basilica Thomson, 1856 in The natural history and morphology of two bromeliad associated hispines from Brazil: Acentroptera basilica Thomson, 1856 and A. cf. tessellata Baly, 1958 (Coleoptera: Chrysomelidae: Cassidinae: Sceloenoplini)
FIGURES 20–25. Acentroptera basilica Thomson, 1856. Pupa: 20, 21, habitus (dorsal, ventral); 22–23, apex of abdomen (dorsal, posterior); 24–25, ventral apex of abdomen (male, female).
FIGURES 7–11. Acentroptera basilica Thomson, 1856 in The natural history and morphology of two bromeliad associated hispines from Brazil: Acentroptera basilica Thomson, 1856 and A. cf. tessellata Baly, 1958 (Coleoptera: Chrysomelidae: Cassidinae: Sceloenoplini)
FIGURES 7–11. Acentroptera basilica Thomson, 1856. Larva: 7–9, head and anterior region of prothorax (dorsal, ventral, lateral); 10, 11, apex of head (dorsal, ventral).
FIGURES 12–19. Acentroptera basilica Thomson, 1856 in The natural history and morphology of two bromeliad associated hispines from Brazil: Acentroptera basilica Thomson, 1856 and A. cf. tessellata Baly, 1958 (Coleoptera: Chrysomelidae: Cassidinae: Sceloenoplini)
FIGURES 12–19. Acentroptera basilica Thomson, 1856. Larva: 12, clypeus and labrum; 13, epipharynx; 14, maxillae and labium; 15, hypopharynx; 16, antenna; 17, leg; 18, 19, mandible (dorsal, ventral).
FIGURES 1–6. Acentroptera basilica Thomson, 1856 in The natural history and morphology of two bromeliad associated hispines from Brazil: Acentroptera basilica Thomson, 1856 and A. cf. tessellata Baly, 1958 (Coleoptera: Chrysomelidae: Cassidinae: Sceloenoplini)
FIGURES 1–6. Acentroptera basilica Thomson, 1856. Larva: 1, 2, habitus (dorsal, ventral); 3, 4, head (dorsal, ventral); 5, segments VII–IX (dorsal); 6, segments VIII–X (ventral).
FIGURE 2 in Helobdella buzz n. sp. (Clitellata: Hirudinida), a bromeliad leech from the Brazilian Atlantic Forest
FIGURE 2. Longitudinal sections of Helobdella buzz. A. Nuchal region showing the internal structure of the protrusion of the skin; B. Segments XII-XIV showing the position of the compact salivary glands (arrow). C. Male (yellow arrow) and female (red arrow) gonopores. D. Genital region showing the compact salivary gland (arrow).
FIGURE 3 in Helobdella buzz n. sp. (Clitellata: Hirudinida), a bromeliad leech from the Brazilian Atlantic Forest
FIGURE 3. Internal morphology of Helobdella buzz. A. atrium; ED. ejaculatory duct; G. ganglium; GC. gastric caecum; O. ovisac; P. proboscis; PC. post-caecum; SD. salivary duct; SG. salivary gland; T. testisac.
FIGURE 1 in Helobdella buzz n. sp. (Clitellata: Hirudinida), a bromeliad leech from the Brazilian Atlantic Forest
FIGURE 1. External morphology of Helobdella buzz. A. Entire leech, dorsal view showing the protrusion of the skin (arrow); B. Entire leech, ventral view; C. Ventral view of the anterior end; D. Dorsal view of the anterior end showing the eyespots (arrows); E. Ventral view of the genital region showing male (M) and female (F) gonopores; F. Lateral view of the anterior end showing the protrusion of the skin (arrow).
Fig. 2 in Longevity and Fecundity of Metamasius quadrilineatus Champion (Coleoptera: Dryophthoridae) on a Natural Bromeliad Host in the Laboratory
Fig. 2. Age-specific egg production by female Metamasius quadrilineatus expressed as (A) percentage of eggs produced relative to the total egg production and (B) mean number of eggs per female per week from six cages each initially containing five male and five female weevils. Vertical bars denote 1 standard error above the mean.
Fig. 3 in Longevity and Fecundity of Metamasius quadrilineatus Champion (Coleoptera: Dryophthoridae) on a Natural Bromeliad Host in the Laboratory
Fig. 3. Metamasius quadrilineatus egg hatch (viability) expressed as the mean percentage of larvae that hatched from a weekly batch of eggs from six cages initially containing five males and female weevils each. Vertical bars denote 1 standard error above the mean.
Fig. 1 in Trigonopeltastes delta (Coleoptera: Scarabaeidae: Cetoniinae) Larva Developing in a Bromeliad Terrarium
Fig. 1. Developmental stages of Mylabris phalerata. A: Egg (2.4 mm); B: L1 (2.6 mm); C: L2 (5.1 mm); D: L3 (13.7 mm); E: L4 (22.4 mm); F: L5 (29.2 mm); G: Pupa (30.1 mm); H: Adult (31.2 mm).
Contrasting reproductive traits affect the genetic diversity and fine-scale genetic structure of two sympatric and epiphytic tropical bromeliads.
<p>This database contains the coordinates of individuals of <em>Aechmea mariae-reginae</em> and <em>Werauhia ampla</em> in phorophytic trees and the genotypes for 8 microsatellite loci.</p>
Litter–trapping tank bromeliads in five different forests: carbon and nutrient pools and fluxes
Bromeliads are the most abundant litter–trapping plants in Neotropical forest canopies. By intercepting litter, bromeliads obtain and retain nutrients before they reach the pedosphere. Here, we analyzed the litter captured and stored by tank bromeliads (TB) in five different forests along an elevation gradient in Mexico. Among those forests, carbon and nutrient pools and nitrogen fluxes in TB were estimated in a mangrove (MF) and a semi–deciduous tropical forest (SDTF). The composition of the litter trapped by TB along the gradient was similar to forest litterfall and was mainly composed of leaves. Most of the litter was captured in the dry season and we found a significant effect of projected plant area and the interaction between month and site on bromeliad litter capture. Moreover, litter stored in TB increased exponentially with projected plant area and differed between three studied species. In the MF (with ca. 2,700 TB ha<sup>-1</sup>), barely ca. 1% of annual litterfall is trapped by these plants, but even in the SDTF, with >10,000 TB ha<sup>-1</sup>, only ca. 2.4% is captured. We found that carbon and nitrogen pools in TB were small and represented < 1% of the carbon and nitrogen stored in forest aboveground biomass. Furthermore, the residence time of litter trapped in TB was not particularly large and was similar to that of litter on the forest floor. In light of our results, we conclude that in the studied forests the effect of TB on the forest carbon and nutrient cycle is negligible.
FIGURE 11 in The Bromeliad Blue Horn Katydid-a new genus of the Cone-headed Katydid (Orthoptera: Tettigoniidae: Conocephalinae: Copiphorini) from the Serra da Jibóia, Bahia, Brazil
FIGURE 11. Micro habitat of Ibityraboia caraguata sp. nov. in Serra da Jibóia, Bahia, Brazil: Male (A) and female (B) in bromeliads.
FIGURE 6 in The Bromeliad Blue Horn Katydid-a new genus of the Cone-headed Katydid (Orthoptera: Tettigoniidae: Conocephalinae: Copiphorini) from the Serra da Jibóia, Bahia, Brazil
FIGURE 6. Ibityraboia caraguata sp. nov., male specimen alive. A: Camouflage posture; B: Walking posture.
FIGURE 5 in The Bromeliad Blue Horn Katydid-a new genus of the Cone-headed Katydid (Orthoptera: Tettigoniidae: Conocephalinae: Copiphorini) from the Serra da Jibóia, Bahia, Brazil
FIGURE 5. Ibityraboia caraguata sp. nov., male internal genitalia. A–B: phallus, ventral view; C–D: phallus, dorsal view; E: phallus with titillator sclerite, ventral view; F: titillator sclerite. Abbreviations: AP: sclerites of apodemes; DF: dorsal fold; DL: dorsal lobe(s); EV: ejaculatory vesicles; TS: titillator sclerite; TI: titillator process; Lw. vl.: lower folds of ventral lobe; Up. vl.: upper folds of ventral lobe.
FIGURE 2 in The Bromeliad Blue Horn Katydid-a new genus of the Cone-headed Katydid (Orthoptera: Tettigoniidae: Conocephalinae: Copiphorini) from the Serra da Jibóia, Bahia, Brazil
FIGURE 2. Ibityraboia caraguata sp. nov., holotype male. A: habitus, dorsal view; B: head, frontal view; C: head and pronotum, dorsal view; D: head and pronotum, lateral view; E: Thoracic sternites, ventral view; F: foreleg, lateral view; G: midleg, lateral view; H: hindleg, lateral view; I–J: Terminalia in ventral and dorsal view respectively; K: Apex of cerci, dorsal view. Abbreviations: Mes: mesobasisternum; Met: metabasisternum; Cer: cerci; Sty: styli; Pl: subgenital plate.
FIGURE 7 in The Bromeliad Blue Horn Katydid-a new genus of the Cone-headed Katydid (Orthoptera: Tettigoniidae: Conocephalinae: Copiphorini) from the Serra da Jibóia, Bahia, Brazil
FIGURE 7. Ibityraboia caraguata sp. nov., paratype female. A: habitus, lateral view; B: head, frontal view; C: head and pronotum, dorsal view; D: head and pronotum, lateral view; E–G: Terminalia in dorsal, ventral and lateral view respectively. Abbreviations: Cer: cerci; Sty: styli; Pl: subgenital plate; Ovp. ovipositor.
FIGURE 3. Hohenbergia ymboreorum. a in Hohenbergia ymboreorum (Bromeliaceae): a new green-flowered bromeliad from Bahia, Brazil
FIGURE 3. Hohenbergia ymboreorum. a) Habit. b) Distal portion of the leaf. c) Primary branch with flowers. d) Flower with and without floral bract. e) Sepal. f) Petal with a stamen. Drawning by Brayan Paiva Cavalcante.
FIGURE 1. Hohenbergia ymboreorum and its habitat. a in Hohenbergia ymboreorum (Bromeliaceae): a new green-flowered bromeliad from Bahia, Brazil
FIGURE 1. Hohenbergia ymboreorum and its habitat. a) General view of habitat (type locality). b) Natural populations in the habitat growing as terrestrial. c) Inflorescences; d) Individual growing as an epiphyte. Photos: a, b) E.H.Souza, c, d) B.P.Cavalcante.
FIGURE 2 in Hohenbergia ymboreorum (Bromeliaceae): a new green-flowered bromeliad from Bahia, Brazil
FIGURE 2. Vegetative and reproductive structures of Hohenbergia ymboreorum. a) Leaves, adaxial and abaxial side. b) Leaf apex. c) Base of the leaf blade showing the prickles. d) Peduncle and the imbricate peduncle bracts. e) Inflorescence (fertile part). f) Peduncle bracts. g) Primary bract. h–i) Spikes with flowers. j) Floral bracts. k) Sepals, (adaxial surface in the middle). l) Petals with the epipetalous stamens. m) Petal appendages. n) Stamens. o) Stigma. Bars: a–c) 4 cm, d) 0.8 cm, e) 3 cm, f–g) 1.2 cm, h–i) 1 cm, j–k) 5 mm, l) 3 mm, m–o) 0.5 mm. Photos: E.H.Souza.
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Allen Brain Atlas
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Annotated Behaviour and Observability Dataset (ABODe)
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