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Figure 5 from: Vikhrev N (2011) Review of the Palaearctic members of the Lispe tentaculata species-group (Diptera, Muscidae): revised key, synonymy and notes on ecology. ZooKeys 84: 59-70. https://doi.org/10.3897/zookeys.84.819

Figure 5 - 1 Lispe sericipalpis Stein, male (Turkey, Antalya) 2 Lispe orientalis Wiedemann, male (Azerbaijan).

Figure 2 from: Vikhrev N (2011) Review of the Palaearctic members of the Lispe tentaculata species-group (Diptera, Muscidae): revised key, synonymy and notes on ecology. ZooKeys 84: 59-70. https://doi.org/10.3897/zookeys.84.819

Figure 2 - Male sternite 5, view from inner side. 1 Lispe tentaculata (De Geer) 2 Lispe draperi Séguy; EP external median process IP internal median process.

Figure 4 from: Vikhrev N (2011) Review of the Palaearctic members of the Lispe tentaculata species-group (Diptera, Muscidae): revised key, synonymy and notes on ecology. ZooKeys 84: 59-70. https://doi.org/10.3897/zookeys.84.819

Figure 4 - Lispe sericipalpis Stein, male lectotype (designated by Pont, 1970). Photo by Joke van Erkelens.

Figure 3 from: Vikhrev N (2011) Review of the Palaearctic members of the Lispe tentaculata species-group (Diptera, Muscidae): revised key, synonymy and notes on ecology. ZooKeys 84: 59-70. https://doi.org/10.3897/zookeys.84.819

Figure 3 - Male terminalia. 1, 2 Lispe sericipalpis Stein, 1 cercal plate 2 sternite 5; 3, 4 Lispe orientalis Wiedemann, 3 cercal plate 4 sternite 5 (from two points of view). <br> In Lispe sericipalpis the cercal plate is more pointed, sternite 5 has the median process thinner and longer.

Figure 1 from: Vikhrev N (2011) Review of the Palaearctic members of the Lispe tentaculata species-group (Diptera, Muscidae): revised key, synonymy and notes on ecology. ZooKeys 84: 59-70. https://doi.org/10.3897/zookeys.84.819

Figure 1 - Male cercal plates. 1 Lispe consanguinea Loew 2 Lispe tentaculata (De Geer) (from Hennig, 1960).

Figures 38-43 from: Sarzetti L, Genise J, Sanchez M, Farina J, Molina A (2013) Nesting behavior and ecological preferences of five Diphaglossinae species (Hymenoptera, Apoidea, Colletidae) from Argentina and Chile. Journal of Hymenoptera Research 33: 63-82. https://doi.org/10.3897/jhr.33.5061

Figures 38-43 - Diphaglossa gayi Spinola, 1851. 38 General view of the nesting site beside the Río Negro Bridge, Chile 39 general view of nesting site at Lonconao, Chile 40 tumulus of soil pellets and open entrance 41 main tunnel 42 nest architecture 43 cell, neck with lining, and egg laying on provisions.

Figures 30-37 from: Sarzetti L, Genise J, Sanchez M, Farina J, Molina A (2013) Nesting behavior and ecological preferences of five Diphaglossinae species (Hymenoptera, Apoidea, Colletidae) from Argentina and Chile. Journal of Hymenoptera Research 33: 63-82. https://doi.org/10.3897/jhr.33.5061

Figures 30-37 - Cadeguala albopilosa (Spinola, 1851). 30 General view of the nest site at Bahia Mansa, Parque Nacional Los Alerces (Chubut province) 31 tumulusof unconsolidated soil32 two main tunnels and longitudinal view of the soil containing a thin ash layer 33 a pair of cells with provisions, necks and lateral tunnels, scale line: 1 cm 34 remains of cells of other nest, scale line: 1 cm 35–36 tomography images of one block of soil containing Cadeguala albopilosa nests, arrows indicate cells 37 3D-reconstruction of one nest and isolate cells.

Figures 8-18 from: Sarzetti L, Genise J, Sanchez M, Farina J, Molina A (2013) Nesting behavior and ecological preferences of five Diphaglossinae species (Hymenoptera, Apoidea, Colletidae) from Argentina and Chile. Journal of Hymenoptera Research 33: 63-82. https://doi.org/10.3897/jhr.33.5061

Figures 8-18 - Ptiloglossa tarsata (Friese, 1900). 8 General view of the nesting site at "La Florida" (Salta province), the arrow indicates the location of the nest; 9 Female of Ptiloglossa tarsata foraging in a flower of Solanum sp. 10 Tumulus of unconsolidated soil, scale line: 1 cm 11 General view showing the nest architecture with a cell at the end of the main tunnel 12 Group of scratches probably produced by female´s mandibles. The arrow indicates their location in the main tunne; 13(a) cell with cellophane-like lining and provisions, (b) neck and (c) entrance tunnel, scale line: 1 cm 14 One cell showing the cellophane-like lining on the wall, scale line: 1 cm 15 Spiral closure of one cell, scale line: 0.5 cm 16 Cocoon operculum with holes, scale line: 0.5 cm 17 Scanning electron micrograph of the cocoon operculum showing the fabric of silk threads with small circular holes, scale: 500 µm 18 Onecircular hole surrounded by silk threads, scale: 50 µm.

Figures 24-29 from: Sarzetti L, Genise J, Sanchez M, Farina J, Molina A (2013) Nesting behavior and ecological preferences of five Diphaglossinae species (Hymenoptera, Apoidea, Colletidae) from Argentina and Chile. Journal of Hymenoptera Research 33: 63-82. https://doi.org/10.3897/jhr.33.5061

Figures 24-29 - Ptiloglossa matutina (Schrottky, 1904). 24 General view of the nesting site at Reserva Karadya, Andresito (Misiones province) 25 Nest entrance closed by a plug of soil(arrow), scale line:1 cm 26 Soil with roots, litter, some rocks, and remains of the main tunnel (arrow) 27 Cell showing the larva partially submerged in provisions, cellophane lining, and the wad cotton-like material attached the cell closure, scale line: 0.5 cm 28 Detail of the cell closure with the cotton-like material 29 Cell and neck wall with the lining removed. Note the high curvature.

Figures 19-23 from: Sarzetti L, Genise J, Sanchez M, Farina J, Molina A (2013) Nesting behavior and ecological preferences of five Diphaglossinae species (Hymenoptera, Apoidea, Colletidae) from Argentina and Chile. Journal of Hymenoptera Research 33: 63-82. https://doi.org/10.3897/jhr.33.5061

Figures 19-23 - 19 Nest architecture of Ptiloglossa tarsata (Friese, 1900). 20 Cell with provisions and egg, cell neck, spiral closure, and entrance tunnel of Ptiloglossa tarsata 21 Nest architecture of Ptiloglossa matutina (Schrottky, 1904) 22 Nest architecture of Cadeguala albopilosa (Spinola, 1851) 23 Cell with provisions and egg, cell neck, location of the cell closure and entrance tunnel of Cadeguala albopilosa.

Figures 1-7 from: Sarzetti L, Genise J, Sanchez M, Farina J, Molina A (2013) Nesting behavior and ecological preferences of five Diphaglossinae species (Hymenoptera, Apoidea, Colletidae) from Argentina and Chile. Journal of Hymenoptera Research 33: 63-82. https://doi.org/10.3897/jhr.33.5061

Figures 1-7 - Zikanapis tucumana (Moure, 1945). 1 General view of the nesting site at Vinchina (La Rioja province) before sunrise 2 Female of Zikanapis tucumana during foraging activity 3 Tumulus, turret andopennest entrance 4 Main and lateral tunnel showing one cell at the end (arrow) 5 General view of nest architecture, scale line: 1 cm 6 Remains of a cell with part of the provisions. Note the curvature of neck 7 Nestarchitecture.

Figure 3 from: Tepe E, Rodríguez-Castañeda G, Glassmire A, Dyer L (2014) Piper kelleyi, a hotspot of ecological interactions and a new species from Ecuador and Peru. PhytoKeys 34: 19-32. https://doi.org/10.3897/phytokeys.34.6376

Figure 3 - Distribution of Piper kelleyi. A Distribution of known localities based on collections (open diamonds) and study plots used to gather natural history data (blue circles) B Predicted distribution based on analysis of habitat parameters using the maximum entropy method. Areas in red are the most likely to have suitable habitat for Piper kelleyi (probability = 0.75–0.87), and areas in blue (0.02–0.08) or unlabeled (< 0.02) are the least likely.

Figure 4 from: Tepe E, Rodríguez-Castañeda G, Glassmire A, Dyer L (2014) Piper kelleyi, a hotspot of ecological interactions and a new species from Ecuador and Peru. PhytoKeys 34: 19-32. https://doi.org/10.3897/phytokeys.34.6376

Figure 4 - A Leaf of Piper kelleyi with characteristic herbivory marks or "windows" made by the specialist herbivore Eois species of Eois that specialize on Piper kelleyi include B Eois viridiflava (Dognin) C Eois aff. viridiflava (Dognin) D Eois ignefumata (Dognin) E Eois planetaria (Dognin) F Eois aff. pallidicosta (Warren) G Eois encina (Dognin) H Eois aff. encina (Dognin).

Figure 2 from: Tepe E, Rodríguez-Castañeda G, Glassmire A, Dyer L (2014) Piper kelleyi, a hotspot of ecological interactions and a new species from Ecuador and Peru. PhytoKeys 34: 19-32. https://doi.org/10.3897/phytokeys.34.6376

Figure 2 - Piper kelleyi. A Habit B Close-up of leaves showing characteristic red color of younger leaves [Tepe et al. 2381] C Close-up of inflorescence [Tepe et al. 2615] D Close-up of infructescence [Tepe et al. 1597].

Figure 1 from: Tepe E, Rodríguez-Castañeda G, Glassmire A, Dyer L (2014) Piper kelleyi, a hotspot of ecological interactions and a new species from Ecuador and Peru. PhytoKeys 34: 19-32. https://doi.org/10.3897/phytokeys.34.6376

Figure 1 - Piper kelleyi Tepe. A leaf and inflorescence B Stamen C fruit in lateral view D Fruit in apical view E Bracts in apical view. [A and E (lower) drawn from Tepe et al. 1597; B–E (upper) drawn from Tepe et al. 2615]

Figure 8 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 8 - Calystegia felix climbing upward through urban landscaping in the City of Chino (Photo M. C. Provance, 2013).

Figure 6 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 6 - The leaves shown here from R.F. Bingham s.n. (UC335392) are consistent with many specimens of Calystegia sepium.

Figure 2 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 2 - Calystegia felix stolons and creeping rootstock. The narrow emergent leaves of this specimen may be atypical; the relatively long petioles are normal (Photo M. C. Provance, 2012).

Figure 7 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 7 - Original material of Convolvulus binghamiae Greene, Santa Barbara, 1886, E.L. Greene s.n. (NDG [NDG-66275]). Flower buds with large clasping bracts typical of the Calystegia sepium complex are noteworthy (a), as is the solitary flower (b) with a broad calyx, broad corolla tube, and a smallish, but otherwise typical clasping bract for the Calystegia sepium complex (Image courtesy of Barbara Hellenthal at the Notre Dame Herbarium).

Figure 5 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 5 - Lectotype of Convolvulus binghamiae Greene, Santa Barbara, July, 1886, R.F. Bingham s.n. (UC335392), with one small bract, and a broad-based corolla.