Find research datasets worth reusing

Figure 4 from: Provance M, Sanders A (2013) Lucky morning glory, Calystegia felix (Convolvulaceae): a new species from Southern California, with notes on the historical ecology of the Chino ciénega belt. PhytoKeys 32: 1-26. https://doi.org/10.3897/phytokeys.32.6020

Figure 4 - Map of historical and recently discovered Calystegia felix occurrences in the Chino Basin. The circled E marks the plant discovered in 2011; normal circles are 2013 occurrences, the largest a cluster of three populations. The broken circle is the approximate location of Johnston's collection in 1917. The perimeter of the Chino artesian belt and "moist land" prior to 1904 is delineated by the thick black line. The street map was adapted from the City of Chino draft general plan EIR, July, 2010, and the artesian belt is based on Mendenhall (1907).

Figure 9 from: Provance M, Sanders A (2013) Lucky morning glory, Calystegia felix (Convolvulaceae): a new species from Southern California, with notes on the historical ecology of the Chino ciénega belt. PhytoKeys 32: 1-26. https://doi.org/10.3897/phytokeys.32.6020

Figure 9 - Emergent Calystegia felix on crusted, moist, Chino silt loam, amongst urban landscaping. It is unknown if large groups of emergent plants such as these represent one to just a few clones, or many genotypes (Photo M. C. Provance, 2013).

Figure 3 from: Provance M, Sanders A (2013) Lucky morning glory, Calystegia felix (Convolvulaceae): a new species from Southern California, with notes on the historical ecology of the Chino ciénega belt. PhytoKeys 32: 1-26. https://doi.org/10.3897/phytokeys.32.6020

Figure 3 - Calystegia felix in bloom at the type locality, in a planter bed in Chino. This plant, discovered in 2011, is the only one we have seen that produces corollas with reddish-purple midpetaline stripes. Also, note the blushed sepals (Photo M. C. Provance, 2011).

Figure 1 from: Provance M, Sanders A (2013) Lucky morning glory, Calystegia felix (Convolvulaceae): a new species from Southern California, with notes on the historical ecology of the Chino ciénega belt. PhytoKeys 32: 1-26. https://doi.org/10.3897/phytokeys.32.6020

Figure 1 - Calystegia felix Provance & A.C. Sanders, sp. nov. The holotype, A.C. Sanders & M.C. and T.A. Provance 40174 (UCR [UCR-246125]). The flowering branchlets are from a single ramet (Photo M. C. Provance, 2011).

Figure 7 from: Bruhl J, Stimpson M, Weston P, Telford I (2012) First instalment in resolution of the Banksia spinulosa complex (Proteaceae): B. neoanglica, a new species supported by phenetic analysis, ecology and geography. PhytoKeys 14: 57-80. https://doi.org/10.3897/phytokeys.14.3415

Figure 7 - Distribution of Banksia neoanglica(solid black circles). Towns and cities indicated by open circles.

Figure 6 from: Bruhl J, Stimpson M, Weston P, Telford I (2012) First instalment in resolution of the Banksia spinulosa complex (Proteaceae): B. neoanglica, a new species supported by phenetic analysis, ecology and geography. PhytoKeys 14: 57-80. https://doi.org/10.3897/phytokeys.14.3415

Figure 6 - Banksia neoanglica at neotype locality. A Habitat B Conflorescences on shrub C Conflorescence from the neotype collection(M.L. Stimpson 180, J.J. Bruhl & I.R. Telford) showing basipetal development; upper flowers with pollen on pollen presentors D Conflorescence and infructescence with black styles at preanthesis. E–G Apex of conflorescences at successive stages of development exhibiting variation in perianth and style colour. Scale bars = 1 cm.

Figure 5 from: Bruhl J, Stimpson M, Weston P, Telford I (2012) First instalment in resolution of the Banksia spinulosa complex (Proteaceae): B. neoanglica, a new species supported by phenetic analysis, ecology and geography. PhytoKeys 14: 57-80. https://doi.org/10.3897/phytokeys.14.3415

Figure 5 - Photograph of the neotype of Banksia spinulosa var. neoanglica A.S.George (M.L. Stimpson 180, J.J. Bruhl & I.R. Telford, NE 98613).

Figure 4 from: Bruhl J, Stimpson M, Weston P, Telford I (2012) First instalment in resolution of the Banksia spinulosa complex (Proteaceae): B. neoanglica, a new species supported by phenetic analysis, ecology and geography. PhytoKeys 14: 57-80. https://doi.org/10.3897/phytokeys.14.3415

Figure 4 - Involucral bracts on young conflorescences in the Banksia spinulosa complex. A Banksia cunninghamii sensu stricto (M.L. Stimpson 122) B Banksia spinulosa sensu stricto (M.L. Stimpson 125) C Banksia neoanglica (M.L. Stimpson 81) D Banksia collina sensu lato (M.L. Stimpson 25A). Scale bar = 2.5 mm.

Figure 3 from: Bruhl J, Stimpson M, Weston P, Telford I (2012) First instalment in resolution of the Banksia spinulosa complex (Proteaceae): B. neoanglica, a new species supported by phenetic analysis, ecology and geography. PhytoKeys 14: 57-80. https://doi.org/10.3897/phytokeys.14.3415

Figure 3 - Common bractson young conflorescences in the Banksia spinulosa species complex: A Banksia neoanglica (BanksiaL. Stimpson 98) B Banksia cunninghamii sensu stricto (M.L. Stimpson 122) C Banksia collina sensu lato (M.L. Stimpson 25A) D Banksia spinulosa sensu stricto. (M.L. Stimpson 120). Scale bar = 1 mm.

Figure 2 from: Bruhl J, Stimpson M, Weston P, Telford I (2012) First instalment in resolution of the Banksia spinulosa complex (Proteaceae): B. neoanglica, a new species supported by phenetic analysis, ecology and geography. PhytoKeys 14: 57-80. https://doi.org/10.3897/phytokeys.14.3415

Figure 2 - Flexible UPGMA phenogram of OTUs in the Banksia spinulosa complex. Major groups from top to bottom: Banksia cunninghamii subsp. cunninghamii, Banksia cunninghamii subsp. A, B. spinulosa var. collina sens. lat., Banksia spinulosa var. spinulosa, Banksia spinulosa from Morisset, Bouddi and Calga. See Table 2 for characters and Appendix 1 for data.

Figure 1 from: Bruhl J, Stimpson M, Weston P, Telford I (2012) First instalment in resolution of the Banksia spinulosa complex (Proteaceae): B. neoanglica, a new species supported by phenetic analysis, ecology and geography. PhytoKeys 14: 57-80. https://doi.org/10.3897/phytokeys.14.3415

Figure 1 - 3D ordination from semi-strong multidimensional scaling of the Banksia spinulosa complex. From to leftto right, Banksia spinulosa var. collina sens. lat., Banksia spinulosa from Morisset, Bouddi and Calga, Banksia spinulosa var. spinulosa, Banksia cunninghamii subsp. cunninghamii, Banksia cunninghamii subsp. A. Ordination stress = 0.795. Size and colour of OTUs represents perspective. Ordination orientated to highlight separation of groups of OTUs. See Table 2 for characters and Appendix 1 for data.

Figure 1 from: Wagstaff S, Clarkson B (2012) Systematics and ecology of the Australasian genus Empodisma (Restionaceae) and description of a new species from peatlands in northern New Zealand. PhytoKeys 13: 39-79. https://doi.org/10.3897/phytokeys.13.3259

Figure 1 - Map showing the generalized distribution of Empodisma in Australia and New Zealand and the collection localities of the DNA samples included in our study. The approximate position of the kauri line in New Zealand is shown with a dashed line.

Figure 12 from: Wagstaff S, Clarkson B (2012) Systematics and ecology of the Australasian genus Empodisma (Restionaceae) and description of a new species from peatlands in northern New Zealand. PhytoKeys 13: 39-79. https://doi.org/10.3897/phytokeys.13.3259

Figure 12 - High resolution photograph of a syntype of Empodisma gracillimum (F.Muell.) L.A.S. Johnson & D.F.Cutler. Mueller (1872–74) originally described the plant as Calorophus gracillimus F.Muell. The specimen, Nouvelle-Hollande, Riv. des cygnes, Preiss JA 1711, 1843, P00748711 is held at HERBARIUM MUSEI PARISIENSIS. The syntype was designated by BG Briggs xi.1998.

Figure 4 from: Wagstaff S, Clarkson B (2012) Systematics and ecology of the Australasian genus Empodisma (Restionaceae) and description of a new species from peatlands in northern New Zealand. PhytoKeys 13: 39-79. https://doi.org/10.3897/phytokeys.13.3259

Figure 4 - Comparison of median networks from independent analyses of trnL, rbcL and matK sequences. Bootstrap values / the number of mutations distinguishing each haplotype. are shown beside the branches. The accessions of Empodisma minus from New Zealand are indicated NZ and Australia Aus.

Figure 11 from: Wagstaff S, Clarkson B (2012) Systematics and ecology of the Australasian genus Empodisma (Restionaceae) and description of a new species from peatlands in northern New Zealand. PhytoKeys 13: 39-79. https://doi.org/10.3897/phytokeys.13.3259

Figure 11 - Morphological characteristics of Empodisma minus. A Vegetative shoot with attached leaves and flowers (2.5× actual size) B Rhizomes with emerging vegetative shoots (2.5× actual size) C Vegetative shoot with attached pistillate flower D Pistillate flower with attached bracts E Gynoecium F Mature nut G Vegetative shoot with attached staminate spikelet H Staminate flower with attached bracts I Staminate flower. Scale bar = 1 mm.

Figure 10 from: Wagstaff S, Clarkson B (2012) Systematics and ecology of the Australasian genus Empodisma (Restionaceae) and description of a new species from peatlands in northern New Zealand. PhytoKeys 13: 39-79. https://doi.org/10.3897/phytokeys.13.3259

Figure 10 - High resolution photograph of the lectotype of Empodisma minus (Hook.f.) L.A.S. Johnson & D.F.Cutler. Reproduced with the consent of the Royal Botanic Gardens, Kew, © The Board of Trustees of the Royal Botanic Gardens. Hooker (1853) described the new species Calorophus minor Hook.f. based upon Bidwell, Colenso and Lyall specimens. A specimen collected near Nelson by Bidwell, no. 84, K000441989, was chosen as the lectotype by Moore and Edgar (1970).

Figure 9 from: Wagstaff S, Clarkson B (2012) Systematics and ecology of the Australasian genus Empodisma (Restionaceae) and description of a new species from peatlands in northern New Zealand. PhytoKeys 13: 39-79. https://doi.org/10.3897/phytokeys.13.3259

Figure 9 - Morphological characteristics of Empodisma robustum. A Vegetative shoot with attached leaves and flowers (actual size) B Rhizomes with emerging vegetative shoots (2.5× actual size) C Vegetative shoot with attached pistillate flower D Pistillate flower with attached bracts E Gynoecium F Mature nut G Vegetative shoot with attached staminate spikelet H Staminate flower with attached bracts I Staminate flower. Scale bar = 1 mm.

Figure 6 from: Wagstaff S, Clarkson B (2012) Systematics and ecology of the Australasian genus Empodisma (Restionaceae) and description of a new species from peatlands in northern New Zealand. PhytoKeys 13: 39-79. https://doi.org/10.3897/phytokeys.13.3259

Figure 6 - Box plots illustrating patterns of morphological variation among the species of Empodisma. The box spans the interquartile range of the values in the variate. The middle 50% of the data lie within the box, with a line showing the median. The whiskers extend beyond the ends of the box as far as the minimum and maximum values.

Figure 7 from: Wagstaff S, Clarkson B (2012) Systematics and ecology of the Australasian genus Empodisma (Restionaceae) and description of a new species from peatlands in northern New Zealand. PhytoKeys 13: 39-79. https://doi.org/10.3897/phytokeys.13.3259

Figure 7 - Principal coordinates ordination depicting patterns of overall similarity among the 74 OTEs that comprised our morphological sample. The first PC axis accounted for 58.3% of the variation in our sample and the second PC axis accounted for 23. 4% of the variation.

Figure 5 from: Wagstaff S, Clarkson B (2012) Systematics and ecology of the Australasian genus Empodisma (Restionaceae) and description of a new species from peatlands in northern New Zealand. PhytoKeys 13: 39-79. https://doi.org/10.3897/phytokeys.13.3259

Figure 5 - Unrooted parsimony tree from a combined analysis of the three sequence partitions. Six distinct cpDNA haplotypes are supported. Bootstrap values / the number of mutations distinguishing each haplotype are shown beside the branches. The accessions of Empodisma minus from New Zealand are indicated NZ and Australia Aus.