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opennotspecifiedJan 2023View details →

FIGURE 1 in "Nicoletia" tergata Mills, 1940 rediscovered in Florida and confirmed as the first species of the Coletiniinae (Zygentoma: Nicoletiidae) in North America

FIGURE 1 Gibboletia tergata (Mills) Ô (K.541617). Foreleg with tarsal articles swollen following mounting in Tendeiro medium. Scale: 0.1 mm.

opennotspecifiedJan 2023View details →

FIGURES 31–41 in "Nicoletia" tergata Mills, 1940 rediscovered in Florida and confirmed as the first species of the Coletiniinae (Zygentoma: Nicoletiidae) in North America

FIGURES 31–41. Gibboletia tergata (Mills) Ô (K.541615 unless otherwise indicated by specimen number). 31) Urosternite III. 32) Urosternite VII. 33) Urosternite VIII. 34) Apex of stylus of urosternite VIII. 35) Coxites IX, penis and detached parameres, the paramere on the left side in dorsal view. 36) Bases of terminal filaments. 37) Scape, pedicel and basal flagellomeres of antenna of ♀ (K.541616). 38) Urotergite X of ♀ (K.541616). 39) Coxites VIII and subgenital plate (K.541616). 40) Coxites IX, styli and ovipositor (K.541616). 41) Apex of ovipositor with location of spinulated area illustrated even though it is on the hidden side of the gonapophysis (K.541616). Scale bars 0.1 mm.

Figure 12 in Aloe ×caesia Salm-Dyck (Asphodelaceae) is the correct name of the common hybrid aloe [Aloe arborescens Mill. × A. ferox Mill.]from the southern Cape, South Africa

Figure 12. Material that Todaro (1889) described and illustrated as Aloe fulgens is clearly identifi- able with some variants, such as this one, of the nothospecies A. ×caesia.

Figure 7 in Aloe ×caesia Salm-Dyck (Asphodelaceae) is the correct name of the common hybrid aloe [Aloe arborescens Mill. × A. ferox Mill.]from the southern Cape, South Africa

Figure 7. Close-up of an inflorescence of Aloe africana × A. ferox. Note how the open flowers flare upwards.

Figure 6 in Aloe ×caesia Salm-Dyck (Asphodelaceae) is the correct name of the common hybrid aloe [Aloe arborescens Mill. × A. ferox Mill.]from the southern Cape, South Africa

Figure 6. Hybrids involving Aloe africana,such as this one with Aloe ferox as the other parent, often have the flowers turned up at anthesis, a character typical of A. africana.

Figure 3 in Aloe ×caesia Salm-Dyck (Asphodelaceae) is the correct name of the common hybrid aloe [Aloe arborescens Mill. × A. ferox Mill.]from the southern Cape, South Africa

Figure 3. The nothospecies (Aloe arborescens × A. ferox) known as A. ×caesia is plentiful in the vicinity of Mosselbaai in South Africa's southern Cape.

Figure 4 in Aloe ×caesia Salm-Dyck (Asphodelaceae) is the correct name of the common hybrid aloe [Aloe arborescens Mill. × A. ferox Mill.]from the southern Cape, South Africa

Figure 4. Aloe africana is a single-stemmed to, more rarely, multi-stemmed species from espe- cially the Jeffrey's Bay-Port Elizabeth-Uitenhage- Grahamstown region of South Africa's Eastern Cape Province.

Figure 8 in Aloe ×caesia Salm-Dyck (Asphodelaceae) is the correct name of the common hybrid aloe [Aloe arborescens Mill. × A. ferox Mill.]from the southern Cape, South Africa

Figure 8. The leaves of some forms of Aloe ×caesia are glaucous green, such as in the case of this form cultivated in the Botanical Garden of the University of Lisbon, Portugal.

Figure 13 in Aloe ×caesia Salm-Dyck (Asphodelaceae) is the correct name of the common hybrid aloe [Aloe arborescens Mill. × A. ferox Mill.]from the southern Cape, South Africa

Figure 13. Plate of Aloe fulgens published in Todaro's Hortus botanicus panormitanus (1889) as Tab. XXXIII, see pp. 40–42.

opencc-zeroJun 2023View details →

Supplementary material 1 from: Pansarin ER, Menezes ELF (2023) A new remarkable Vanilla Mill. (Orchidaceae) species endemic to the Espinhaço Range, Brazil: its phylogenetic position and evolutionary relationships among Neotropical congeners. PhytoKeys 227: 151-165. https://doi.org/10.3897/phytokeys.227.101963

Species of Vanilla included in the molecular study, their locations, vouchers and GenBank accession numbers

opennotspecifiedSep 2021View details →

Fig. 7 in Flavonoids in the flowers of Primula × polyantha Mill. and Primula primulina (Spreng.) H. Hara (Primulaceae)

Fig. 7. Fresh flower colors of Primula × polyantha cultivars, and their major pigments. (For interpretation of the references to color in this figure legend, the reader is referred to the Web version of this article.)

opennotspecifiedSep 2021View details →

Fig. 3 in Flavonoids in the flowers of Primula × polyantha Mill. and Primula primulina (Spreng.) H. Hara (Primulaceae)

Fig. 3. Chemical structures of anthocyanins 1 and 6, isolated from the violetblue flowers of Primula ×polyantha cultivars and P. primulina. Observed important NOEs are indicated by arrows. Observed important HMBCs are indicated by dotted arrows. (For interpretation of the references to color in this figure legend, the reader is referred to the Web version of this article.)

opennotspecifiedSep 2021View details →

Fig. 4 in Flavonoids in the flowers of Primula × polyantha Mill. and Primula primulina (Spreng.) H. Hara (Primulaceae)

Fig. 4. Chemical structures of known anthocyanins isolated from the flowers of Primula × polyantha cultivars.

opencc-by-4.0Aug 2023View details →

Pulp mill pinch data

<p>Data set utilized to construct grand composite curve of a pulp mill.</p>

Fig. 3 in Terpenylated coumarins from the root bark of Ailanthus altissima (Mill.) Swingle

Fig. 3. Key NOESY correlations of compounds 1–4, 5 and 6 (1D NOESY correlations were marked in red and 2D NOESY correlations were marked in blue).

Fig. 2 in Terpenylated coumarins from the root bark of Ailanthus altissima (Mill.) Swingle

Fig. 2. Key HMBC correlations (arrows in blue) and H1–H1 COSY (bold bond in black) of the undescribed compounds.

Fig. 4 in Terpenylated coumarins from the root bark of Ailanthus altissima (Mill.) Swingle

Fig. 4. (A) Possible gross structures of compounds 3, 4 and 11; (B) Possible relative configurations of compound 3 (3b1/3b2) and 4 (4b1/4b2).

Fig. 6 in Structural characterization of the Pet c 1.0201 PR-10 protein isolated from roots of Petroselinum crispum (Mill.) Fuss

Fig. 6. Visualization of amino acid residues (yellow) that stabilize dimers and are responsible for IgE binding (red) in A: Api g 1.0101 (template 2BK0); B: Pet c 1.0201 in water; C: Pet c 1.0201 in 0.2 M salt. (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)

Fig. 5 in Structural characterization of the Pet c 1.0201 PR-10 protein isolated from roots of Petroselinum crispum (Mill.) Fuss

Fig. 5. Evolution of the inter-monomeric distances during the MD simulation with relative dispositions of monomeric units at the beginning (0 ns) and the end (200 ns) of each simulation. A: Api g 1.0101 in water; B: Pet c 1.0201 in water; C: Pet c 1.0201 in 0.2 M NaCl. Relative positions at 0 ns and after 200 ns for respective black and red trajectories are visualized; the blue trajectory shows a breakdown of a dimeric form into monomer units. (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)

Fig. 1 in Structural characterization of the Pet c 1.0201 PR-10 protein isolated from roots of Petroselinum crispum (Mill.) Fuss

Fig. 1. IEF-PAGE (A) and SDS-PAGE (B) of the Coomassie Brilliant blue stained proteins purified from the Petroselinum crispum roots. (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)