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Figs 21–24 in Redescription of Omophoita octoguttata (Coleoptera: Chrysomelidae) and its immature stages, with notes on life history
Figs 21–24. Omophoita octoguttata (Fabricius, 1775), pupa, habitus: 21, dorsal; 22, ventral; 23, cocoons made from soil matter with pupa; 24, interior of the cocoon, pupa removed. Scale bar = 1 mm.
Figs 19, 20 in Redescription of Omophoita octoguttata (Coleoptera: Chrysomelidae) and its immature stages, with notes on life history
Figs 19, 20. Omophoita octoguttata (Fabricius, 1775), mature larva: 19, head, frontal view (DOS, dorsoepicranial setae; POS, paraocellar setae; PFS, posterofrontal setae; EFS, externofrontal setae; AFS, anterofrontal setae; EES, externoepicranial setae); 20, lateral habitus. Scale bar = 1 mm.
Figs 16–18 in Redescription of Omophoita octoguttata (Coleoptera: Chrysomelidae) and its immature stages, with notes on life history
Figs 16–18. Omophoita octoguttata (Fabricius, 1775): 16, terrarium used for the rearing; 17, clutch of eggs buried in soil within the terrarium;18, egg. Scale = 1 mm.
Figs 5–9 in Redescription of Omophoita octoguttata (Coleoptera: Chrysomelidae) and its immature stages, with notes on life history
Figs 5–9.Omophoita octoguttata (Fabricius, 1775), mouthparts of the adult: 5, labrum, frontal view; 6, left maxilla, dorsal view (I-V, maxillary palpomeres; LCN, lacinia; GLA, galea; BST, basistipe; DST, disistipe; CRD, cardo); 7, labium, ventral view (MNT, mentum; PRM, prementum; LGL, ligula); 8, 9, mandibles, frontal view: 8, right; 9, left (I-V, mandibular teeth; MSL, membranous setose lobe). Scale bar = 500 μm.
Figs 13–15 in Redescription of Omophoita octoguttata (Coleoptera: Chrysomelidae) and its immature stages, with notes on life history
Figs 13–15. Omophoita octoguttata (Fabricius, 1775), female genitalia: 13, tignum; 14, spermatheca; 15, vaginal palpi (RCP, receptacle; DCT, spermathecal duct). Scale = 200 μm.
Figs 10–12 in Redescription of Omophoita octoguttata (Coleoptera: Chrysomelidae) and its immature stages, with notes on life history
Figs 10–12. Omophoita octoguttata (Fabricius, 1775), male genitalia: 10, median lobe, dorsal view; 11, aedeagus, right lateral view; 12, detail of the apical hood of the median lobe, dorsal view (APH, apical hood; BHS, basal hooks; BOR, basal orifice; LTL, lateral lobes; MDL, middle lobe). Scale = 200 µm.
Figs 1–4 in Redescription of Omophoita octoguttata (Coleoptera: Chrysomelidae) and its immature stages, with notes on life history
Figs 1–4. Omophoita octoguttata (Fabricius, 1775). Dorsal habitus with color pattern variations: 1, female; 2, male. Frontal view of the head: 3, variant with rectangular maculae, female; 4, variant with rounded maculae, male.
Fig. 8 in The postcranial skeleton of the Early Triassic parareptile Sauropareion anoplus, with a discussion of possible life history
Fig. 8. Strict consensus of 45 optimal trees discovered in PAUP 4.0b10 analysis of a modified version of the data matrix from MacDougall and Modesto (2011). Tree length = 155, consistency index (CI) = 0.72, CI excluding uninformative characters = 0.71, rescaled CI = 0.56.
Fig. 6 in The postcranial skeleton of the Early Triassic parareptile Sauropareion anoplus, with a discussion of possible life history
Fig. 6. Procolophonid Sauropareion anoplus Modesto, Sues, and Damiani, 2001, from Lower Triassic Katberg Formation, Vangfontein, Middelburg District, South Africa; NMQR 3602. Interpretive drawings of skull in right lateral (A) and left lateral (B) views, and right forelimb in medial view (C).
Fig. 5 in The postcranial skeleton of the Early Triassic parareptile Sauropareion anoplus, with a discussion of possible life history
Fig. 5. Procolophonid Sauropareion anoplus Modesto, Sues, and Damiani, 2001, from Lower Triassic Katberg Formation, Vangfontein, Middelburg District, South Africa; NMQR 3602. Photograph of skeleton in dorsal view (A) and interpretive drawing of skeleton in dorsal view (B). Arabic numbers indicate presacral vertebrae. Roman numerals indicate digits.
Fig. 3 in The postcranial skeleton of the Early Triassic parareptile Sauropareion anoplus, with a discussion of possible life history
Fig. 3. Procolophonid Sauropareion anoplus Modesto, Sues, and Damiani, 2001, from Lower Triassic Katberg Formation, Vangfontein, Middelburg District, South Africa; NMQR 3556. Photograph of skeleton in dorsal view (A) and interpretive drawing of skeleton in dorsal view (B). Areas without outlines represent impression.
Fig. 4 in The postcranial skeleton of the Early Triassic parareptile Sauropareion anoplus, with a discussion of possible life history
Fig. 4. Procolophonid Sauropareion anoplus Modesto, Sues, and Damiani, 2001, from Early Triassic Katberg Formation, Vangfontein, Middelburg District, South Africa; NMQR 3556. Interpretive drawings of skull in right lateral view (A) and left lateral view (B). Areas without outlines represent impression.
Fig. 1 in The postcranial skeleton of the Early Triassic parareptile Sauropareion anoplus, with a discussion of possible life history
Fig. 1. Procolophonid Sauropareion anoplus Modesto, Sues, and Damiani, 2001, from Lower Triassic Katberg Formation, Vangfontein, Middelburg District, South Africa; NMQR 3544. Interpretive drawing of skeleton in dorsal view. Areas without outlines represent impression. Arabic numbers indicate presacral vertebrae.
Fig. 2 in The postcranial skeleton of the Early Triassic parareptile Sauropareion anoplus, with a discussion of possible life history
Fig. 2. Procolophonid Sauropareion anoplus Modesto, Sues, and Damiani, 2001, from Lower Triassic Katberg Formation, Vangfontein, Middelburg District, South Africa; NMQR 3544. Interpretive drawings of skull in palatal (A), right lateral (B), and left lateral (C) views. Areas without outlines represent impression.
Fig. 4. A in Life history strategies of Cotylurus spp. Szidat, 1928 (Trematoda, Strigeidae) in the molecular era - Evolutionary consequences and implications for taxonomy
Fig. 4. A median-joining network of COI haplotype of Cotylurus. Each circle represents a unique haplotype where the diameter is proportional to the number of DNA sequences represented.
Fig. 1 in Life history strategies of Cotylurus spp. Szidat, 1928 (Trematoda, Strigeidae) in the molecular era - Evolutionary consequences and implications for taxonomy
Fig. 1. The phylogenetic relationships within genus Cotylurus based on the concatenated COI mtDNA and 28S rDNA markers. The analysis was performed by the use of Bayesian inference, diamond symbol indicates posterior probability greater than 90%.
Fig. 3 in Life history strategies of Cotylurus spp. Szidat, 1928 (Trematoda, Strigeidae) in the molecular era - Evolutionary consequences and implications for taxonomy
Fig. 3. The phylogenetic relationships within the genus Cotylurus based on COI mtDNA marker. The analysis was performed by the use of Bayesian inference, diamond symbol indicates posterior probability greater than 90%.
Fig. 2 in Life history strategies of Cotylurus spp. Szidat, 1928 (Trematoda, Strigeidae) in the molecular era - Evolutionary consequences and implications for taxonomy
Fig. 2. The phylogenetic relationships within the genus Cotylurus based on 28S rDNA marker. The analysis was performed by the use of Bayesian inference, diamond symbol indicates posterior probability greater than 90%.
Fig. 4 in Reproductive life history of Heterandria bimaculata (Heckel, 1848) (Poeciliinae: Poeciliidae) in the Honduran interior highlands: trait variation along an elevational gradient
Fig. 4. Changes in reproductive traits of female Heterandria bimaculata along an elevational gradient in Cusuco National Park, Honduras in summer 2013. Points represent actual values. Dashed lines represent fitted means from linear mixed models, accounting for nested effects of individual variability within sites, and total length of individuals. No fitted line is presented for reproductive allotment because this variable did not change significantly along the elevational gradient.
Fig. 3 in Reproductive life history of Heterandria bimaculata (Heckel, 1848) (Poeciliinae: Poeciliidae) in the Honduran interior highlands: trait variation along an elevational gradient
Fig. 3. Changes in physicochemical parameters of streams along an elevation gradient in Cusuco National Park, Honduras in summer 2013.
ScienceDex guides
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These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.
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International Brain Laboratory public data
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OpenNeuro
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