197 results on '"Dippenaar-Schoeman, A. S."'
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2. Coexistence of Ammoxenus (Gnaphosidae) spider species on and between termitaria of Microhodotermes viator (Hodotermitidae) at a Karoo site
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Henschel, Joh, primary, Dean, W. Richard J., additional, Milton, Suzanne J., additional, and Dippenaar-Schoeman, Ansie S., additional
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- 2023
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3. Burrow structure and microhabitat characteristics of Nesiergus insulanus (Araneae: Theraphosidae) from Frégate Island, Seychelles
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Canning, Gregory, Reilly, Brian K, Dippenaar-Schoeman, Ansie S, and BioStor
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- 2014
4. The faunistic diversity of spiders (Arachnida: Araneae) of the South African Cape Floristic Kingdom.
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Dippenaar-Schoeman, A. S., Haddad, C. R., Foord, S. H., and Lotz, L. N.
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SPIDERS , *ARACHNIDA , *JUMPING spiders , *SPECIES distribution , *RELATIONAL databases , *WOLF spiders - Abstract
Spider species distribution in the Cape Floristic Kingdom (CFK) was compiled as part of the South African National Survey of Arachnida (SANSA), whose main aim was to create a relational database for the country's arachnid fauna. Data from the CFK was extracted from taxonomic and faunistic published papers, as well as unpublished faunistic survey data in national collections. A total of 11 500 records from 130 localities were recorded in the CFK until the end of 2023, representing 62 families, 334 genera and 960 species, with two further families (Synotaxidae and Theridiosomatidae) only known from undescribed species. This represents 42.4% of the total spider fauna of South Africa. For each species, the global and CFK distribution, as well as the level of endemicity and a conservation assessment using the IUCN Red List criteria, are provided. A total of 269 spp. (28.0%) are endemic to the CFK, 49 spp. (5.1%) are of special concern, and 229 spp. (23.9%) are Data Deficient. However, most of the species (682 spp., 71.0%) have a wide distribution with no known threats and are categorised as Least Concern. Salticidae is the most species-rich family (128 spp.), with 30 spp. endemic to the CFK, followed by the Gnaphosidae (107 spp.), Thomisidae (86 spp.) and Lycosidae (49 spp.), while six families are represented by a single species. The last decade has seen an exponential growth in the knowledge of spiders in South Africa, and there are certainly many more species that must still be discovered and described. [ABSTRACT FROM AUTHOR]
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- 2024
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5. Supplementary material 2 from: Dippenaar-Schoeman AS, Haddad CR, Lotz LN, Booysen R, Steenkamp RC, Foord SH (2023) Checklist of the spiders (Araneae) of South Africa. African Invertebrates 64(3): 221-289. https://doi.org/10.3897/AfrInvertebr.64.111047
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Dippenaar-Schoeman, Ansie S., primary, Haddad, Charles R., additional, Lotz, Leon N., additional, Booysen, Ruan, additional, Steenkamp, Rudolph C., additional, and Foord, Stefan H., additional
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- 2023
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6. Figure 2 from: Dippenaar-Schoeman AS, Haddad CR, Lotz LN, Booysen R, Steenkamp RC, Foord SH (2023) Checklist of the spiders (Araneae) of South Africa. African Invertebrates 64(3): 221-289. https://doi.org/10.3897/AfrInvertebr.64.111047
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Dippenaar-Schoeman, Ansie S., primary, Haddad, Charles R., additional, Lotz, Leon N., additional, Booysen, Ruan, additional, Steenkamp, Rudolph C., additional, and Foord, Stefan H., additional
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- 2023
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7. Figure 3 from: Dippenaar-Schoeman AS, Haddad CR, Lotz LN, Booysen R, Steenkamp RC, Foord SH (2023) Checklist of the spiders (Araneae) of South Africa. African Invertebrates 64(3): 221-289. https://doi.org/10.3897/AfrInvertebr.64.111047
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Dippenaar-Schoeman, Ansie S., primary, Haddad, Charles R., additional, Lotz, Leon N., additional, Booysen, Ruan, additional, Steenkamp, Rudolph C., additional, and Foord, Stefan H., additional
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- 2023
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8. Supplementary material 1 from: Dippenaar-Schoeman AS, Haddad CR, Lotz LN, Booysen R, Steenkamp RC, Foord SH (2023) Checklist of the spiders (Araneae) of South Africa. African Invertebrates 64(3): 221-289. https://doi.org/10.3897/AfrInvertebr.64.111047
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Dippenaar-Schoeman, Ansie S., primary, Haddad, Charles R., additional, Lotz, Leon N., additional, Booysen, Ruan, additional, Steenkamp, Rudolph C., additional, and Foord, Stefan H., additional
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- 2023
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9. Figure 1 from: Dippenaar-Schoeman AS, Haddad CR, Lotz LN, Booysen R, Steenkamp RC, Foord SH (2023) Checklist of the spiders (Araneae) of South Africa. African Invertebrates 64(3): 221-289. https://doi.org/10.3897/AfrInvertebr.64.111047
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Dippenaar-Schoeman, Ansie S., primary, Haddad, Charles R., additional, Lotz, Leon N., additional, Booysen, Ruan, additional, Steenkamp, Rudolph C., additional, and Foord, Stefan H., additional
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- 2023
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10. Checklist of the spiders (Araneae) of South Africa
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Dippenaar-Schoeman, Ansie S., primary, Haddad, Charles R., additional, Lotz, Leon N., additional, Booysen, Ruan, additional, Steenkamp, Rudolph C., additional, and Foord, Stefan H., additional
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- 2023
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11. THE INFLUENCE OF MOUND STRUCTURE ON THE DIVERSITY OF SPIDERS (ARANEAE) INHABITING THE ABANDONED MOUNDS OF THE SNOUTED HARVESTER TERMITE TRINERVITERMES TRINERVOIDES
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Haddad, Charles R, Dippenaar-Schoeman, Anna S, and BioStor
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- 2002
12. DIVERSITY OF SPIDERS (ARANEAE) IN A SAVANNA RESERVE, NORTHERN PROVINCE, SOUTH AFRICA
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Whitmore, Cheryl, Slotow, Rob, Crouch, Tanza E, Dippenaar-Schoeman, Ansie S, and BioStor
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- 2002
13. The effect of elevation and time on mountain spider diversity: a view of two aspects in the Cederberg mountains of South Africa
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Foord, Stefan H. and Dippenaar-Schoeman, Anna S.
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- 2016
14. The Influence of Mound Structure on the Diversity of Spiders (Araneae) Inhabiting the Abandoned Mounds of the Snouted Harvester Termite Trinervitermes trinervoides
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Haddad, Charles R. and Dippenaar-Schoeman, Anna S.
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- 2002
15. Notes on the biology of Pycnacantha tribulus, another araneid without an orbweb (Araneae: Araneidae)
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Dippenaar-Schoeman, Anna S, Leroy, Astri, and BioStor
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- 1996
16. Insights into the karyotype and genome evolution of haplogyne spiders indicate a polyploid origin of lineage with holokinetic chromosomes
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Král, Jiří, Forman, Martin, Kořínková, Tereza, Lerma, Azucena C. Reyes, Haddad, Charles R., Musilová, Jana, Řezáč, Milan, Herrera, Ivalú M. Ávila, Thakur, Shefali, Dippenaar-Schoeman, Ansie S., Marec, František, Horová, Lucie, and Bureš, Petr
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- 2019
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17. Checklist of the spiders (Araneae) of South Africa.
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Dippenaar-Schoeman, Ansie S., Haddad, Charles R., Lotz, Leon N., Booysen, Ruan, Steenkamp, Rudolph C., and Foord, Stefan H.
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SPIDERS , *JUMPING spiders , *ARACHNIDA , *ORB weavers , *DATABASES , *SUBSPECIES - Abstract
A checklist of 2265 spider species and subspecies, 495 genera and 71 families is provided. Data were extracted from the South African National Survey of Arachnida database and over 200 taxonomic revisions, ending December 2022. Global distributions, endemicity and conservation assessment using IUCN Criteria are provided for each species. A total of 1325 spp. are endemic to South Africa (58.5%), 126 spp. (5.6%) are of special concern and 693 spp. (30.6%) are Data Deficient (DD), while 15 species were described without exact locality data. Most species (1444 spp., 63.8%) are widely distributed with no known threats and are of Least Concern. A total of 1316 spp. (57.6%) are known from both sexes and 23 spp. (1.0%) were described from juveniles. Salticidae is the most speciesrich family (354 spp.), followed by Gnaphosidae (195 spp.), Thomisidae (143 spp.) and Araneidae (100 spp.) and ten families are represented by a single species. [ABSTRACT FROM AUTHOR]
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- 2023
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18. Notes on the butterfly theridiid Episinus marignaci (Lessert, 1933) (Araneae, Theridiidae) from South Africa
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Dippenaar-Schoeman, Anna S. and Foord, Stefan H.
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Angola ,South African National Survey of Arachnida ,geographical distribution - Abstract
We present the first records of the butterfly theridiid Episinus marignaci (Lessert, 1933) beyond its type locality, resulting in an extension of its geographic range from Angola to South Africa. Images of live specimens and a dis-tribution map are provided. Episinus marignaci is rare locally but has a relatively large geographical distribution in South Africa.
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- 2022
19. Notes on the butterfly theridiid Episinus marignaci (Lessert, 1933) (Araneae, Theridiidae) from South Africa
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Dippenaar-Schoeman, Anna S., primary and Foord, Stefan H., additional
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- 2022
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20. FOOD STORAGE BY A WANDERING GROUND SPIDER (ARANEAE, AMMOXENIDAE, AMMOXENUS)
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Dippenaar-Schoeman, Ansie S, Harris, Rupert, and BioStor
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- 2005
21. Spider Responses to Alien Plant Invasion: The Effect of Short- and Long-Term Chromolaena odorata Invasion and Management
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Mgobozi, Mandisa P., Somers, Michael J., and Dippenaar-Schoeman, Ansie S.
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- 2008
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22. Associations of Spiders of the Genus Peucetia (Oxyopidae) with Plants Bearing Glandular Hairs
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Vasconcellos-Neto, João, Romero, Gustavo Q., Santos, Adalberto J., and Dippenaar-Schoeman, Ansie S.
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- 2007
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23. Parabomis elsae Dippenaar-Schoeman & Foord 2020, sp. nov
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Dippenaar-Schoeman, Anna S. and Foord, Stefan H.
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Parabomis elsae ,Arthropoda ,Arachnida ,Animalia ,Araneae ,Biodiversity ,Thomisidae ,Parabomis ,Taxonomy - Abstract
Parabomis elsae sp. nov. Figures 4–7 Etymology. Named after Elsa van Niekerk (Pretoria South Africa), the graphic artist at Agricultural Research Council (ARC)—Plant Health and Protection, in recognition of her support for spider research at the ARC. Diagnosis. Males and females of this species are recognized by their mottled bodies and copulatory organs (Figs 4, 5). Parabomis elsae sp. nov. females resemble those of P. megae sp. nov. in the shape of the epigyne, but the colour differs by being strongly mottled in P. elsae sp. nov. In males of both species the RTA apex is directed dorsad, but in P. elsae sp. nov. the RTA apex is claw-like (Fig. 6). Description. Holotype male. Measurements: TL 1.8; CL 0.85; CW 0.95. Legs: I 1.42 (0.51, 0.12, 0.30, 0.27, 0.22) II; 1.42 (0.63, 0.21, 0.28, 0.20, 0.10); III 1.08 (0.34, 0.12, 0.32, 0.20, 0.10); IV 1.32 (0.47, 0.15, 0.32, 0.19, 0.19). Carapace fawn, with 3 faint yellowish bands, one medially other 2 radiating from PLE to posterior edge (Fig. 4); darker patches laterally; integument granulose, with scattered small tubercles, with scattered short, thick, flat-lying setae, more numerous laterally; carapace slightly wider than long. Chelicerae brown; mouthparts paler brown. Sternum pale brown; integument granulose. Legs brown, same as in carapace; femora and tibiae slightly darker; articulation area of joints with strong white rim. Abdomen dorsum shield-like; with dark brown patches, with paler transverse patches in between, sides grey, speckled with white. Male palp with RTA tip claw-like curving upwards; VTA small fused with RTA (Fig. 6). Female. Measurements: TL 3.36; CL 1.36; CW 1.36. Legs: I 1.93 (0.68, 0.29, 0.43, 0.25, 0.28); II 1.84 (0.60, 0.27, 0.44, 0.25, 0.28); III 1.23 (0.42, 0.24, 0.26, 0.12, 0.19); IV 1.74 (0.56, 0.46, 0.29, 0.31, 0.12). Resembles male. Carapace fawn, with strong mottled appearance; 3 faint yellowish bands, one medially other two radiating; darker patches laterally; clypeus and eye area with three infused medial bands; clypeus paler (Fig. 5); carapace as wide as long; integument granulose, with scattered small tubercles. Chelicerae pale yellow, mouthparts yellowish brown. Sternum yellowish brown; integument granulose. Legs brown, strongly mottled with white, base of setae brown giving legs spotted appearance; articulation area of joints with strong white rim. Abdomen dorsum creamish white, base of abdominal setae dark, giving abdomen strong spotted appearance, especially anteriorly. Epigyne atrium wider than long, egg-shaped, with lateral edges slightly thickened (Fig. 7); intromittent orifices uncovered and situated in anterior part; spermatheca with two lobes (Fig. 8). Type material. Holotype ³: SOUTH AFRICA: Gauteng Province: Roodeplaat Dam Nature Reserve (West), 17 km NE of Pretoria, 28º22’S, 25º37’E, leg. A.S. Dippenaar-Schoeman, 5.XI.1981 (beating Vachelia trees) (NCA 82 /492). Paratypes: SOUTH AFRICA: Gauteng Province, Roodeplaat Dam Nature Reserve (West), 17 km NE of Pretoria, 28º22’S, 25º37’E, leg. A.S. Dippenaar-Dippenaar, 27.XI.1979 (beating flowering Acacia trees, spider collected from yellow flowers), 1♀ (NCA 80/277); Same locality, leg. A.S. Dippenaar-Schoeman, 17.XII.1981 (sweeping grass), 1³ (NCA 81/1091); Same locality, leg. National Collection of Arachnida staff, 22.IX.1988 (beating Acacia trees), 1³, 2 imm. (NCA 92/607). Other material examined. SOUTH AFRICA: Gauteng Province: Enkeldoorn, 25°24’S, 28°40’E, leg. A.S. Dippenaar-Schoeman, 6.VIII.1974 (sweeping grass), 4imm. (NCA 76 /298); Roodeplaatdam Nature Reserve, 28º22’S, 25º37’E, leg. M. Stiller, 29.IX.1980 (sweeping grass), 1imm. (NCA 1992 /608); Same locality, leg. M. Stiller, 13.VIII.1980 (sweeping grass), 1imm. (NCA 1981 /862); Same locality, leg. A.S. Dippenaar-Schoeman, 27.XI.1980 (sweeping grass), 2imm. (NCA 1999 /34). KwaZulu-Natal Province: iSimangaliso Wetland Park, Hell’s Gate, 28º01.2’S, 32º21.6’E, leg. J. Esterhuizen, 1.XI.2004 (blue trap), 1³ (NCA 2020 /547); Same locality data, 3.VIII.2008 (blue trap), 1³ (NCA 2020 /548); Same locality data, 20.IX.2004 (blue trap), 2³, 1imm. (NCA 2020 /549); iSimangaliso Wetland Park, False Bay Park, 27º58.8’S 32º21.72’E, leg. M. Hamer, 6.XI.2004 (tree beating), 1³, 1imm. (NCA 2006 /58). Limpopo Province: Rust de Winter, 25°13’S, 28°29’E, leg. A.S. Dippenaar-Schoeman, 30. IV.1981 (beating grass), 1♀, 1imm. (NCA 99 /35); Polokwane Nature Reserve, 23º58’S, 29º28’E, leg. T. Khoza & M. Modiba, 3. II.2006 (riverine and sweet thorn ticket, tree beating), 1³, 1♀ (NCA 2008 /2204). Mpumalanga Province: Loskopdam Nature Reserve, 25°46’S, 29°23’E, leg. A.S. Dippenaar-Schoeman, 2. IV.1973 (sweeping grass), 1imm. (NCA 2009 /455). Distribution. South Africa: Gauteng, Limpopo, KwaZulu-Natal, and Mpumalanga Provinces (Fig. 32). Biology/Habitat. Specimens have been mainly collected beating flowering Vachellia trees and sweeping grass in the Savanna Biome. Adults were sampled from September to December., Published as part of Dippenaar-Schoeman, Anna S. & Foord, Stefan H., 2020, Revision of the Afrotropical crab-spider genus Parabomis Kulczyński, 1901 (Araneae: Thomisidae), pp. 161-174 in Zootaxa 4899 (1) on page 164, DOI: 10.11646/zootaxa.4899.1.8, http://zenodo.org/record/4400882
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- 2020
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24. Parabomis pilosus Dippenaar-Schoeman & Foord 2020, sp. nov
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Dippenaar-Schoeman, Anna S. and Foord, Stefan H.
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Parabomis pilosus ,Arthropoda ,Arachnida ,Animalia ,Araneae ,Biodiversity ,Thomisidae ,Parabomis ,Taxonomy - Abstract
Parabomis pilosus sp. nov. Figures 1, 2, 21 – 25 Etymology. The name refers to the numerous setae on the carapace of the species. Diagnosis. The male of this species differs from all the other congeners by the blunt RTA (Fig. 23) vs. pointed in other species. In the female, the epigyne atrium is bell-shaped (Fig. 24) and contrasts with that of P. martini, which is subtriangular. Carapace and abdomen bearing rows of flat-lying translucent club-shaped setae that are longer and denser than in other species, especially on the carapace declivity (Fig. 22). Description. Male (holotype). TL 1.7; CL 0.9; CW 1.0. Legs: I 1.43 (0.51, 0.13, 0.30, 0.27, 0.22); II 1.43 (0.63, 0.22, 0.28, 0.20, 0.10); III 1.09 (0.34, 0.12, 0.32, 0.21, 0.10); IV 1.32 (0.47, 0.15, 0.32, 0.19, 0.19). Carapace dark brown, granular, with numerous white club-shaped setae (Fig. 21); carapace edge white; eyes circled with black; chelicerae dark brown; mouthparts yellowish brown; carapace wider than long. Sternum orange brown, granulose, bearing numerous strong flat-lying translucent setae. Legs with coxae, trochanters and tibiae brown, with white articulations. Abdomen broad, dorsum dark brown, shield-like, with pale patches; granular. Palp: RTA not pointed but with blunt broad apex (Fig. 23); VTA absent. Female. TL 2.6; CL 1.05; CW 1.3; CH 1.4; AW 2.1; AL 2.1. Legs: Legs: I 1.88 (0.65, 0.29, 0.42, 0.25, 0.27); II 1.81 (0.60, 0.26, 0.43, 0.24, 0.28); III 1.20 (0.42, 0.21, 0.26, 0.12, 0.19); IV 1.7 (0.55, 0.46, 0.26, 0.31, 0.12). Carapace fawn with clypeus and eye region infused with brown, lateral edges darker brown; chelicerae and mouthparts yellowish white; posterior declivity clothed with numerous white flat-lying club-shaped setae (Figs 1-2, 22). Sternum yellowish white. Legs fawn to brown infused with white; femora darker, especially legs II and III; articulate area of each leg segment with white rim. Abdomen fawn to white, with faint spots; depressions on abdomen darker, bearing two brownish triangular to round patches. Epigyne: atrium bell-shaped (Fig. 24); spermathecae oval, spermathecal ducts short, glandular lobes anteriorly of spermathecae (Fig. 25). Type material. Holotype ³: BOTSWANA: Okavango Delta, Shakawe Fishing Camp, 18°26’S, 21°54’E, leg. J. van Niekerk, 1.XII.2001 (active searching) (NCA 2006 /868). Paratypes: BOTSWANA: Okavango Delta, Xugana Island, 130 km NNW of Maun, 19°04’S, 23°03’E, leg. B.H. Lamoral, 17–25.XI.1980, 1♀ (NMSA 23719); Okavango Delta, 30 km N of Lechwee Camp, approx. between 18°40’S– 19°00’S and 23°00’E– 23°45’E, leg. B. Lamoral, 17-20.XI.1979, 1³ (NMSA); Okavango Delta, N of Lechwee Camp and Khwai River Lodge, between 18°40’S– 19°00’S and 23°00’E– 23°45’E, leg. B. Lamoral, 18- 20.XI.1979, 2³ (NMSA); Okavango Delta, near Shakawe, Lesideng Research Camp, 18°25’S, 21°53’E, leg. R. Lyle, 10-20.XII.2006 (beating shrubs in riverine forest), 1♀ (NCA 2020 /550). Other material examined. BOTSWANA: Okavango Delta, Xugana Island, 130 km NNW of Maun, 19°04’S, 23°03’E, leg. F. Nyathi, 17-25.XI.1980, 1♀ (NMZ / A 70941). SOUTH AFRICA: Limpopo Province: Tshipise, Farm Alicedale (citrus), 22°42’S, 30°14’E, leg. J. Wilkinson, 12.IV.2016 (on tree in silk retreat, see Figs 1-2), 1♀ (SANSA Virtual Museum). Distribution. Known from Botswana and northern South Africa (Fig. 32). Biology/Habitat. Specimens were sampled by sweeping grass and herbs. In Tshipise, a female was sampled from a silk retreat made between leaves., Published as part of Dippenaar-Schoeman, Anna S. & Foord, Stefan H., 2020, Revision of the Afrotropical crab-spider genus Parabomis Kulczyński, 1901 (Araneae: Thomisidae), pp. 161-174 in Zootaxa 4899 (1) on pages 170-171, DOI: 10.11646/zootaxa.4899.1.8, http://zenodo.org/record/4400882
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- 2020
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25. Parabomis megae Dippenaar-Schoeman & Foord 2020, sp. nov
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Dippenaar-Schoeman, Anna S. and Foord, Stefan H.
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Arthropoda ,Arachnida ,Animalia ,Araneae ,Parabomis megae ,Biodiversity ,Thomisidae ,Parabomis ,Taxonomy - Abstract
Parabomis megae sp. nov. Figures 15 – 20 Etymology. Named in honour of Ms Meg Cumming (Harare, Zimbabwe), in recognition of her contribution to our knowledge of Zimbabwean spiders. Diagnosis. The species is distinguished from other congeners by the male palp having the RTA straight, with the apex directed dorsally, while directed laterad in others, except for P. elsae sp. nov. It differs from P. elsae sp. nov. by the sharply pointed tip of the apex (Fig. 18). Parabomis megae sp. nov. resembles the female of P. elsae sp. nov. in the shape of the epigyne, but the colour differs, being uniform in P. megae sp. nov. and strongly mottled in P. elsae sp. nov. (Fig. 19). Description. Male (holotype). Measurements: TL 1.90; CL 0.95; CW 1.03. Legs: I 1.44 (0.52, 0.13, 0.30, 0.27, 0.22); II 1.44 (0.63, 0.22, 0.28, 0.20, 0.11); III 1.09 (0.34, 0.12, 0.32, 0.21, 0.10); IV 1.32 (0.47, 0.15, 0.32, 0.19, 0.19). Carapace dark brown (Fig. 15); eyes circled with black; chelicerae dark brown; mouthparts yellowish brown; palp dark brown; carapace slightly wider than long; strongly granulated, bearing numerous small tubercles, each with translucent seta. Sternum brown; granulose. Eyes as for genus. Legs: coxae, trochanters and tibiae brown, with blackish hue; femora I-IV dark brown, with femora I and II usually darker than rest; patellae yellowish brown; tibiae, metatarsi and partly tarsi of legs I and II clothed with numerous fine erect setae. Abdomen dorsum white with brown hue, shield-like with scattered black spots. Male palp with RTA straight, tip directed dorsally and apex pointed (Fig. 18). Female. Measurements: TL 3.2; CL 1.1; CW 1.4. Legs: I 1.83 (0.67, 0.29, 0.42, 0.25, 0.27); II 1.84 (0.61, 0.28, 0.43, 0.24, 0.28); III 1.61 (0.41, 0.22, 0.26, 0.12, 0.70); IV 1.71 (0.55, 0.46, 0.27, 0.31, 0.12). Carapace fawn, in some specimens darker laterally (Figs 16-17); strongly granulated, bearing numerous small tubercles, each with translucent seta; eye region infused with white; eyes sometimes circled with black; chelicerae creamish white. Sternum granulated, bearing tubercles with seta. Legs creamish white, with distinct white bands at joints; femora frequently darker. Abdomen fawn to white, with scattered dark setae giving it spotted appearance; depressions on dorsum darker, bearing two brownish markings (Fig. 16). Epigyne with atrium oval (Fig. 19); spermathecae with short ducts (Fig. 20). Type material. Holotype ³: ZIMBABWE: Doddieburn Dam, Doddieburn Ranch, 21°28’S, 29°24’E, leg. J. Minshull, 12.XII.1985 (NMZ / A4208 a). Paratypes: ZIMBABWE: Doddieburn Dam, Doddieburn Ranch, 21°28’S, 29°24’E, leg. J. Minshull, 12.XII.1985, 1♀, 3³, 4imm. (NMZ / A4208 b); Tshowe River rapids, Matetsi Safari Area, 18°31’S, 28°40’E, leg. J. Minshull, 6.XII.1988, 1³ (NMZ A6916); Walmer Drive, Harare, 17°49’S, 31°05’E, leg. M. Cumming, 14. VI.2004 (spider ballooning), 1♀ (NCA 2012 /327); Same locality data, leg. M. Cumming, 15.I.2004 (sweeping grass and herbs in garden), 1♀, 3imm. (NCA 2012 /326); Same locality data, leg. M. Cumming, 1. III.2004, 1♀ (NCA 2009 / 258). Other material examined. ZIMBABWE: Humani Ranch, Store Camp, 20°29’S, 32°15’E, leg. Falcon College, 6. IV.1987, 1imm. (NMZ A 5882); Doddieburn Dam, Doddieburn Ranch, 21°28’S, 29°24’E, leg. E. Nyathi, 20. IV.1986, 2 imm. (NMZ / A4661); Same locality, leg. J. Minshull, 11.XII.1985, 1 imm. ♀ (NMZ 4227); Chelo Farm Homestead, 2029A3, leg. F. Nyathi, 5.X.1988, 5 imm. (NMZ 715), 4 imm. (NMZ / A7190); Namakukwe, Zambezi confluence, 17°51’S, 25°23’E, leg. Falcon College, 26.VIII.1986, 1 imm. (NMZ 4794); Sabi-Lundi confluence, Gomarezhou National Park, 21°23’S, 33°50’E, leg. J. Minshull, 21. IV.1985, 1 imm. (NMZ 3289); Tshowe River rapids, Matetsi Safari Area 18°31’S, 28°40’E, leg. J. Minshull, 4.XII.1988 (NMZ 6895); Katombora Campsite, 17°50’S, 25°24’E, leg. Falcon College, 1.X.1986, 1 imm. (NMZ 4720), 1 imm. NMZ 5040, 1 imm NMZ 5079, 1 imm. NMZ 5086); 1.5 km NW of Kazuma Forestry camp, 1825B3, leg. Falcon College, 15. IV.1988, 2 imm. (NMZ / A 6704); Farm 2 km E. Glenmore, 2028C, leg. F.Nyathi, 28.IX.1988, 1 imm. (NMZ / A 7094); Sengwa Plot, leg. M. Cumming, 2.XII.2002 (beating Trichelias tree), 1³ (NCA 2009 /456). Distribution. Known only from Zimbabwe (Fig. 32). Biology/Habitat. Specimens were sampled sweeping grass and herbs. Most of the adult specimens were sampled from December to March., Published as part of Dippenaar-Schoeman, Anna S. & Foord, Stefan H., 2020, Revision of the Afrotropical crab-spider genus Parabomis Kulczyński, 1901 (Araneae: Thomisidae), pp. 161-174 in Zootaxa 4899 (1) on pages 168-169, DOI: 10.11646/zootaxa.4899.1.8, http://zenodo.org/record/4400882
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26. Parabomis wandae Dippenaar-Schoeman & Foord 2020, sp. nov
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Dippenaar-Schoeman, Anna S. and Foord, Stefan H.
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Parabomis wandae ,Arthropoda ,Arachnida ,Animalia ,Araneae ,Biodiversity ,Thomisidae ,Parabomis ,Taxonomy - Abstract
Parabomis wandae sp. nov. Figures 26 – 30 Etymology. This species is named in honour of Prof Wanda Wesołowska (Wrocław, Poland), in recognition of her significant contributions to the taxonomy of African and Palaearctic Salticidae. Diagnosis. Male of this species differ from congeners in the shape of the RTA that is almost as long as the width of the bulb, with the tip directed laterad (Fig. 28). The RTA base is broad and the apex is beak-like, in contrast to the sharply pointed apex of P. martini. The abdomen has a hump that is more distinct in males, while in P. martini the abdomen profile is round. The atrium of the female epigyne is egg-shaped, as wide as long, with the ventral edge thickened (Fig. 29), and the spermathecal ducts are long and curved (Fig. 30). Description. Holotype male. Measurements: TL 1.90; CL 0.91; CW 0.95. Legs: I 1.45 (0.52, 0.12, 0.31, 0.28, 0.22); II 1.45 (0.63, 0.23, 0.29, 0.20, 0.10); III 1.08 (0.34, 0.12, 0.32, 0.20, 0.10); IV 1.31 (0.46, 0.15, 0.32, 0.19, 0.19). Carapace: dark brown, darker laterally, strongly granulated, bearing numerous small tubercles, each with translucent seta (Fig. 26); eyes circled with black; chelicerae brown; mouthparts yellowish brown. Sternum brown, granulate. Legs dark; coxae, trochanters and tibiae brown, with blackish hue; femora I–IV dark brown, with femora I–II usually darker than rest; patellae yellowish brown; all legs with distinct white bands at joints distinct when viewed from below. Abdomen dorsum with brown scutum, with scattered black patches; in lateral view with distinct hump; white laterally and pale below. Palp with large beak-like RTA (Fig. 28); tip directed laterad with small VTA. Female. Measurements: TL 2.26; CL 0.97; CW 1.10. Legs: I 1.90 (0.67, 0.29, 0.42, 0.25, 0.27), II 1.82 (0.60, 0.27, 0.43, 0.24, 0.28); III 1.21 (0.42, 0.22, 0.26, 0.12, 0.19); IV 1.42 (0.55, 0.16, 0.28, 0.31, 0.12). Resembles the male but larger in size and paler in colour (Fig. 27). Carapace fawn to brown, with dark patch laterally; eyes circled with black; eye region infused with white; chelicerae fawn; integument strongly granulated, bearing numerous small tubercles, each with translucent seta. Sternum granulated, bearing tubercles with setae. Legs same colour as prosoma; white with distinct white bands at joints; femora darker. Abdomen white with dark patches, scattered dark setae giving it spotted appearance; abdomen with hump less distinct than in male. Epigyne with sub-oval atrium, slightly wider than long, edges slightly thickened (Fig. 29); spermathecae slightly longer than wide, with long curving spermathecal ducts (Fig. 30). Type material. Holotype ³: GHANA: Kakum Forest, 05°21’N, 01°23’W, leg. R. Jocqué et al., 17.XI.2005 (fogging secondary forest) (MRAC 218.012). Paratypes: GHANA: Kakum Forest, °21’N, 01°23’W, 21.XI.2005 (fogging primary forest), leg. R. Jocqué et al., 1♀ 2³ (MRAC 218052); Same locality data, leg. R. Jocqué, et al., 15.XI.2005 (fogging secondary forest), 1³ (MRAC 217.977). KENYA: Kakamega Forest, 00°22’N, 34°50’E, leg. W. Freund, 10.IX.2002 (canopy fogging), 1♀ (ZFMK AR133). Other material examined. GHANA: Kakum Forest, 05°21’N, 01°23’W, leg. R. Jocqué et al., 22.XI.2005 (fogging secondary forest), 1³ (MRAC 218.058). KENYA: Kakamega Forest, 00°22’N, 34°50’E, leg. W. Freund, 10.IX.2002 (canopy fogging), 1³ (ZFMK AR129), 1³ (ZFMK AR051), 1³ (ZFMK AR052), 1³ (ZFMK AR053), 1³ (ZFMK AR054), 1³ (ZFMK AR132). IVORY COAST: Appouesso, FC Bossematié station 5, 06°36’N, 03°27’W, leg. R. Jocqué & L. Baert, 15.X.1993 (sweeping), 1³ (MRAC 205.437); Bettie, forest close to Mabi, leg. R. Jocqué, 3.XI.1993 (sweeping forest edge), 1♀ (MRAC 177.635). RWANDA: Ibanda Makera, 02°20’S, 29°39’E, 1.X.1993 (fogging montane forest), 1♀, 4³ (ZFMK, thom 12). Distribution. Known from Ghana, Kenya, Rwanda and Ivory Coast (Fig. 32). Biology/Habitat. Collected from primary and secondary forest while fogging the canopy of trees. One male was collected in the Ivory Coast while sweeping vegetation. Adults were sampled from September to November., Published as part of Dippenaar-Schoeman, Anna S. & Foord, Stefan H., 2020, Revision of the Afrotropical crab-spider genus Parabomis Kulczyński, 1901 (Araneae: Thomisidae), pp. 161-174 in Zootaxa 4899 (1) on pages 171-172, DOI: 10.11646/zootaxa.4899.1.8, http://zenodo.org/record/4400882
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27. Parabomis Kulczynski 1901
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Dippenaar-Schoeman, Anna S. and Foord, Stefan H.
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Arthropoda ,Arachnida ,Animalia ,Araneae ,Biodiversity ,Thomisidae ,Parabomis ,Taxonomy - Abstract
Parabomis Kulczyński, 1901 Parabomis Kulczyński, 1901: 3, 30, figs 25–27; Simon 1903: 1011; Lessert 1919: 181; Ono 1988: 207; Dippenaar-Schoeman 2014: 244. Type species. Parabomis levanderi Kulczyński, 1901. Diagnosis. Parabomis shares with the other four African genera of the Bominae the globular body shape, small size and very short legs without spines. They share with Thomisops and Holopelus the peg-like setae on the promargins of the chelicerae, which are absent in Avelis and Felsina. It can be distinguished from Avelis, Thomisops and Holopelus by the high carapace (carapace height> carapace length), the very broad sloping clypeus, as well as the eyes that are grouped far apart,> 0.6 × clypeus width (Fig. 1). Parabomis male palps differ from those of the other African genera in having both a ventral apophysis and strongly developed retrolateral apophysis on the tibia. The marginally sclerotized atrium of Parabomis differs from Holopelus and Thomisops in the absence of a hood, and from Avelis in the absence of a median septum. Description. Female. Total length varies between 3.1–3.6 mm. Carapace cream to brown, sometimes tinted with green (Fig. 3), frequently mottled with white in eye region and on clypeus, with darker patches laterally, as seen in live specimens (Figs 1–3). Carapace as wide as long, anteriorly only slightly narrower than posteriorly; thoracic region high and convex, with distinct posterior declivity; declivity edge with semicircular carina with row of polyp-like tubercles, each bearing a short club-shaped seta; integument granulose, with scattered small tubercles, bearing very short, thick, flat-lying setae, more numerous laterally (very distinct in P. pilosus sp. nov. (Fig. 1)). Eyes small; both eye rows recurved, with AER shorter than PER and strongly recurved; lateral eyes on small tubercles, with posterior tubercle slightly larger than anterior tubercle; AME closer to ALE than to each other; ALE same size as AME; PME closer to PLE than to each; PME slightly smaller than PLE; MOQ much wider than long, slightly wider anteriorly than posteriorly. Clypeus distinct, strongly sloping, protruding slightly over cheliceral base; edge curved. Chelicerae flattened anteriorly; promargin bearing densely packed bristle-like setae. Labium longer than wide. Sternum cream to dark; narrow-oval, prolonged posteriorly to form an obtuse point between legs IV; integument granulose. Legs same color as carapace, varying from cream to pale brown, in some species mottled with white, with articulation areas of each leg segment frequently with distinct white rims; legs short and thick; patellae nearly as long as metatarsi; tibiae longer than metatarsi; macro-setae absent, legs bearing short hair-like setae; tarsi with numerous teeth on paired claw; metatarsi and tarsi in some species with strong erect setae ventrally. Abdomen creamish white to brown, with darker hue in dorsal depressions (Figs 1–3); rounded, wider than long; shape varying from ball-shaped (when swollen with food or eggs) (Fig. 17) to slightly flattened, with lateral and transverse striae sometimes forming deep depressions; striae bearing small tubercles, each with translucent club-shaped seta; abdomen closely pressed against cephalothorax, fitting into posterior declivity; ventral region pale. Epigyne with marginally sclerotized atrium, of which shape varies from sub-oval, triangular to bell-shaped; spermathecae simple, longer than wide, bilobed sac-like structures, short, simple copulatory ducts, with intromittent orifices uncovered and situated in anterior part. Male: Total length varies between 1.7–2.03 mm. Males resemble females but differ as follows: smaller in size; carapace and legs darker than female, usually uniformly brown; abdomen dorsum darker, shield-like in appearance, white laterally; dorsal depressions dark; legs slightly more slender than females; tibiae, metatarsi and tarsi bearing long dense setae ventrally. Palp: femur and patella not modified; tibia with two apophyses, VTA smaller than RTA, both fused; RTA about same length as tibia, apex pointed; shape varying between species; cymbium as long as wide, tutaculum absent; tegulum round, lacking apophyses; embolus filiform at tip, originating at 9h00 position. Distribution. Parabomis is endemic to the Afrotropical Region and was previously known from Bioko Island (Fernando Poo), Cameroon, Eritrea, Equatorial Guinea (Spanish Guinea), Namibia and Tanzania. New records: Botswana, Ghana, Guinea, Kenya, Malawi, Nigeria, Rwanda, South Africa, Zanzibar and Zimbabwe., Published as part of Dippenaar-Schoeman, Anna S. & Foord, Stefan H., 2020, Revision of the Afrotropical crab-spider genus Parabomis Kulczyński, 1901 (Araneae: Thomisidae), pp. 161-174 in Zootaxa 4899 (1) on pages 162-163, DOI: 10.11646/zootaxa.4899.1.8, http://zenodo.org/record/4400882, {"references":["Kulczynski, W. (1901) Arachnoidea in Colonia Erythrea a Dre K. M. Levander collec a de Cracovie. Memoires et Comptes rendus des seances de la section des mathematiques et des sciences naturelles de l'Academie des sciences, 41, 1 - 63.","Simon, E. (1903) Arachnides de la Guinee espagnole. Memoires de la Societe d'histoire naturelle de Paris, 1 (3), 65 - 124.","Lessert, R. de (1919) Araignees du Kilimandjaro et du Merou (suite). III. Thomisidae. Revue Suisse de Zoologie, 27, 99 - 234. https: // doi. org / 10.5962 / bhl. part. 36325","Ono, H. (1988) A revisional study of the spider family Thomisidae (Arachnida, Araneae) of Japan. National Science Museum, Tokyo and New Publishing Co. Ltd., Tokyo, 252 pp.","Dippenaar-Schoeman, A. S. (2014) Field guide to the Spiders of South Africa. Lapa Publishers, Pretoria, 432 pp."]}
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28. Parabomis levanderi Kulczynski 1901
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Dippenaar-Schoeman, Anna S. and Foord, Stefan H.
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Parabomis levanderi ,Arthropoda ,Arachnida ,Animalia ,Araneae ,Biodiversity ,Thomisidae ,Parabomis ,Taxonomy - Abstract
Parabomis levanderi Kulczyński, 1901 Figures 9 Parabomis levanderii Kulczyński, 1901: 3, 30, figs 25–27 (Holotype ³: ERITREA: Ghinda, 15°27’N, 39°05’E, leg. K.M. Levander, FMNH—examined). Diagnosis. Males resemble those of P. martini in colour and the shield-like abdomen, but in P. levanderi the dorsum has two longitudinal series of black spots dorsally in depressions, which are absent in P. levanderi. Parabomis levanderi is the only male where the palp has the RTA two-pronged, with the one lobe longer and slightly hooked (Fig. 9). Description. Holotype male. Measurements: TL 1.9; CL 1.1; CW 1.1. Legs: I 2.17 (0.65, 0.35, 0.47, 0.36, 0.34); II 2.14 (0.65, 0.34, 0.46, 0.36, 0.33); III (missing); IV 1.64 (0.52, 0.29, 0.34, 0.23, 0.26). Carapace chestnut brown, with dark patches laterally; posterior declivity yellow; clypeus mottled, with paler longitudinal infusions; carapace as wide as long, with deep posterior declivity; edge of declivity bearing numerous small tubercles; integument with scattered tubercles, each bearing club-shaped seta. Mouthparts and chelicerae paler than carapace. Sternum dark reddish brown, with narrow white margin, integument granulose. Legs: coxae dark; trochanters yellow; anterior femora black; patella yellow; anterior tibiae dark reddish brown; tarsi dark red; each segment distinctly rimmed with white. Abdomen: dorsum white, with shield-like dark area. Male palp with small fused VTA, RTA two-pronged (Fig. 9). Female. Unknown. Distribution. Known only from the type locality (Fig. 32)., Published as part of Dippenaar-Schoeman, Anna S. & Foord, Stefan H., 2020, Revision of the Afrotropical crab-spider genus Parabomis Kulczyński, 1901 (Araneae: Thomisidae), pp. 161-174 in Zootaxa 4899 (1) on pages 165-166, DOI: 10.11646/zootaxa.4899.1.8, http://zenodo.org/record/4400882, {"references":["Kulczynski, W. (1901) Arachnoidea in Colonia Erythrea a Dre K. M. Levander collec a de Cracovie. Memoires et Comptes rendus des seances de la section des mathematiques et des sciences naturelles de l'Academie des sciences, 41, 1 - 63."]}
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29. Revision of the Afrotropical crab-spider genus Parabomis Kulczyński, 1901 (Araneae: Thomisidae)
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DIPPENAAR-SCHOEMAN, ANNA S., primary and FOORD, STEFAN H., additional
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- 2020
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30. A list of spider species found in the Addo Elephant National Park, Eastern Cape province, South Africa
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Dippenaar-Schoeman, Anna S., primary, Wiese, Linda, additional, Foord, Stefan H., additional, and Haddad, Charles R., additional
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- 2020
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31. Food Storage by a Wandering Ground Spider (Araneae, Ammoxenidae, Ammoxenus)
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Dippenaar-Schoeman, Ansie S.
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- 2005
32. Spider checklist for the Blouberg, in the Vhembe Biosphere Reserve, South Africa
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Foord, Stefan, primary, Dippenaar-Schoeman, Anna S., additional, Haddad, Charles R., additional, Schoeman, Colin, additional, Hahn, Norbert, additional, and Lyle, Robin, additional
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- 2019
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33. Assessing local scale impacts of Opuntia stricta (Cactaceae) invasion on beetle and spider diversity in Kruger National Park, South Africa
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Robertson, M. P., Harris, K. R., Coetzee, J. A., Foxcroft, L. C., Dippenaar-Schoeman, A. S., and Berndt van Rensburg
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Araneae, arthropods, Coleoptera, invasion impacts, invasive plants, non-native, Opuntia stricta - Abstract
There is a paucity of studies examining direct impacts of introduced alien species on biodiversity, a key need for motivating for alien species control in conservation areas. The introduced prickly pear (Opuntia stricta) has invaded some 35 000 ha of Kruger National Park. We investigated the effect of O. stricta on beetle and spider species assemblages in the Skukuza region of Kruger National Park. We used unbaited pitfall traps over a 12-month period in four treatments of varying O. stricta density. Species richness, species density and abundance of beetles and spiders were compared. A total of 72 beetle and 128 spider species were collected. Species richness and species density for beetles and spiders did not differ significantly across the four treatments. Assemblages for spiders did not differ across treatments but beetle assemblages were significantly different from uninvaded control sites. This study suggests that the current density of O. stricta does not significantly affect spider species richness, density or assemblages but that beetle assemblages are significantly affected.Key words: Araneae, arthropods, Coleoptera, invasion impacts, invasive plants, non-native, Opuntia stricta.
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- 2017
34. Effects of a fast-burning spring fire on the ground-dwelling spider assemblages (Arachnida: Araneae) in a central South African grassland habitat
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Haddad, Charles R., Foord, Stefan H., Fourie, René, and Dippenaar-Schoeman, Anna S.
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abundance, Free State, management, resistance, season, species richness - Abstract
Fire is widely used as a management strategy in grasslands to maintain vegetation structure and improve grazing quality for large herbivores. The impacts of burning on invertebrates in South Africa remain poorly understood. A study was initiated in spring 2005 to determine the impact of a fast hot burn on ground-dwelling spider assemblages in a grassland habitat in the central Free State. Pitfall traps were set out at six sites in the reserve, with three sites each in the burnt and unburnt areas, to sample spiders over a 12-month period. A total of 5 253 spiders were collected, representing 33 families and 120 species. Spider abundance was significantly lower in the burnt (n = 1 956) than unburnt sites (n = 3 297), and burnt sites had, on average, considerably fewer species than unburnt sites. The dominant families in the burnt sites were Lycosidae (29.5%), Gnaphosidae (16.9%), Ammoxenidae (9.6%) and Zodariidae (5.7%), whereas Ammoxenidae (22.7%), Lycosidae (20.6%), Gnaphosidae (15.3%) and Amaurobiidae (10.2%) dominated the unburnt sites. Of the nine most abundant families collected, only Caponiidae were more abundant in the burnt than unburnt sites. Our data suggest that fast-burning hot spring fires cause a considerable initial post-fire decline in spider abundance, and have a negative influence on the abundance as well as the resistance of assemblages to disturbances other than fire (e.g. rain). However, most of the dominant families had abundances comparable to unburnt areas within a year post-burn.Keywords: abundance, Free State, management, resistance, season, species richness
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- 2017
35. South African National Survey of Arachnida: A checklist of the spiders (Arachnida, Araneae) of the Tswalu Kalahari Reserve in the Northern Cape province, South Africa
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Dippenaar-Schoeman, Anna S., primary, Haddad, Charles R., additional, Lyle, Robin, additional, Lotz, Leon N., additional, Foord, Stefan H., additional, Jocque, Rudy, additional, and Webb, Peter, additional
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- 2018
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36. Aspects of the ecology and behaviour of the Seychelles theraphosid Nesiergus insulanus (Arachnida: Araneae: Theraphosidae)
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Canning, Gregory, Reilly, Brian Kevin, and Dippenaar-Schoeman, Ansie S.
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Biodiversity ,Taxonomy - Abstract
Canning, Gregory, Reilly, Brian Kevin, Dippenaar-Schoeman, Ansie S. (2015): Aspects of the ecology and behaviour of the Seychelles theraphosid Nesiergus insulanus (Arachnida: Araneae: Theraphosidae). African Invertebrates 56 (1): 167, DOI: 10.5733/afin.056.0113, URL: http://www.bioone.org/doi/10.5733/afin.056.0113
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- 2015
37. Leroya silva Honiball Lewis & Dippenaar-Schoeman 2014, sp. n
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Honiball Lewis, Allet S. and Dippenaar-Schoeman, Ansie S.
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Arthropoda ,Arachnida ,Animalia ,Araneae ,Biodiversity ,Thomisidae ,Leroya ,Leroya silva ,Taxonomy - Abstract
Leroya silva sp. n. Figs 128–136, 139, 143–144, 147 Type material: Holotype: ♂, DEMOCRATIC REPUBLIC OF CONGO (DRC): Bas Congo-Region, Mayombe, Luki Forest Reserve [5°37’S, 13°05’E], fogging, 5–10 November 2006, D. De Bakker & J.P. Michiels (MRAC 222238a). Paratypes: DEMOCRATIC REPUBLIC OF CONGO (DRC): 2 ♂, 1 ♀, collected with holotype (MRAC 222238b); 1 juvenile ♀, 2 ♂ same locality data as holotype (MRAC 220995). RWANDA: Est Province , 1 ♀, Ibanda Makera [02°09’S, 30°55’E], October 1993, T. Wagner (ZFMK AR 1320 ) . UGANDA: Masindi Province, 1 ♂, Budongo forest [01°45’N, 31°25’E], 15–25 January 1997, T. Wagner (ZFMK AR 1321). Etymology. “ Silva ” is the Latin word that means forest, and it refers to the habitat where all known individuals were sampled. Noun in apposition. Diagnosis. Body without patterns (Figs 133, 135). Differs from L. unicolor in slightly darker body, shape of copulatory organs and carapace that is wider than long. Epigyne visible as two sclerotised areas (Figs 136, 143), in L. unicolor visible as one large sclerotised area. Male bulb as in Figs 134, 141, 142. Description. Female. Size, measurements (n = 3). TL: 4.10 (3.89–4.22); CL: 1.98 (1.91–2.04); CW: 2.00 (1.96–2.05); CI: 0.99 (0.97–1.03); CH: 0.99 (0.74–1.11); CLL: 0.20 (0.19–0.23); MOQ-L: 0.37 (0.34–0.37). Colour. Carapace with metallic-shine to copper-brown; eye tubercles copper; abdomen dorsally and ventrally pale brown (Fig. 135). Carapace. Slightly wider than long. Clypeus. With numerous thick, long setae on edge. Chelicerae. With short setae (Fig. 128). Sternum. SL: 0.85; SW: 0.84; SI: 1.02. Eye s. Eye spots on all eyes or only on LE; ALE and PLE situated on very flatish tubercles; eye measurements: AME–AME: 0.57; ALE–AME: 0.60; AME–AME/AME–ALE: 0.94; PME–PME: 0.72; PLE–PME: 0.68; PME–PME/PME–PLE: 1.07; ALE/AME: 1.07; PLE/PME: 0.94; MOQ-AW/MOQ-PW: 0.97; MOQ-L/MOQ-W: 0.46; Clyp/AME–AME: 0.36. Legs. With trichobothria, tarsal claws with long tufts that extend densely towards claws (Figs 129–132); leg formula: I:II:III:IV; leg measurements: leg I—Fe 1.47, Pat 0.57, Tib 1.39, Mt 1.14, Ta 0.81, total 5.38; II—Fe 1.48, Pat 0.46, Tib 1.28, Mt 1.15, Ta 0.80, total 5.17; III—Fe 1.10, Pat 0.38, Tib 0.78, Mt 0.62, Ta 0.51, total 3.40; IV—Fe 1.04, Pat 0.37, Tib 0.81, Mt 0.67, Ta 0.50, total 3.39. Abdomen. With numerous long and shorter setae, spiniform setae scattered in between, all embedded in distinct tubercles; sigillae bigger than other species. AL: 2.12; AW: 2.05; AI: 1.03. Epigyne. Spermathecae and intromittent canals as in Figs. 143, 144. Male. Size, measurements (n = 3). TL: 3.39 (3.04–3.92); CL: 1.63 (1.42–1.94); CW: 1.68 (1.49–2.00); CI: 0.97 (0.95–0.99); CH: 0.82 (0.68–0.93); CLL: 0.20 (0.15–0.26); MOQ-L: 0.31 (0.28–0.35). Resemble females but differ as follows: Colour. Metallic-shine, copper or blackish-turquoise; abdomen dorsally and ventrally dark brown (Fig. 133). Clypeus. As in Fig. 139. Sternum. SL: 0.67 SW: 0.70 SI: 0.96. Eyes. Eye measurements: AME–AME: 0.47; ALE–AME: 0.50; AME–AME/AME–ALE: 0.93; PME–PME: 0.56; PLE–PME: 0.59; PME–PME/PME–PLE: 0.95; ALE/AME: 1.08; PLE/PME: 1.05; MOQ-AW/MOQ-PW: 0.83; MOQ-L/MOQ-W: 0.37; Clyp/AME– AME: 0.41. Legs. Leg formula: II:I:III:IV; leg measurements: leg I—Fe 0.99, Pat 0.28, Tib 1.00, Mt 0.84, Ta 0.54, total 3.65; II—Fe 1.50, Pat 0.41, Tib 1.44, Mt 1.20, Ta 0.77, total 5.32; III—Fe 0.97, Pat 0.29, Tib 0.71, Mt 0.57, Ta 0.45, total 2.98; IV—Fe 0.86, Pat 0.28, Tib 0.72, Mt 0.56, Ta 0.45, total 2.87. Abdomen. AL: 1.75; AW: 1.67; AI: 1.05. Palp. Bulb with slight swelling laterally; tibia with long setae; RTA and VTA long (Figs 134, 141, 142). Natural history. This species lives in the canopy of rainforests. Adults and juveniles were collected from October until January. Distribution. Democratic Republic of Congo (DRC), Rwanda, Uganda (Fig. 147).
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38. Mystaria stakesbyi Honiball Lewis & Dippenaar-Schoeman 2014, sp. n
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Honiball Lewis, Allet S. and Dippenaar-Schoeman, Ansie S.
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Arthropoda ,Mystaria stakesbyi ,Mystaria ,Arachnida ,Animalia ,Araneae ,Biodiversity ,Thomisidae ,Taxonomy - Abstract
Mystaria stakesbyi sp. n. Figs 5, 38, 39, 83–86, 126 Type material: Holotype: ♀, GHANA: Greater Accra Region, Legon [05°39’N, 00°11’W], 10 December 1969, P.A. Room (MRAC 135.996). Paratypes: DEMOCRATIC REPUBLIC OF CONGO (DRC): Kasai-Occidental Province, 1 ♀, Luebo [05°20’S, 21°25’E], 1992, D.H Schouteden (MNHG). Nord-Kivu Region, 1 ♂, Kivu, Semliki, Valley of Djuma [00°43’N, 29°45’E], leaf litter sifting, 15 July 1968, R.P.M. Lejeune (MRAC 135.812); 1 ♀, Rutshuru [01°10’S, 29°27’E], April 1937, J. Ghesquierie (MRAC 20812/20816). GABON: Estuaire Region, 1 ♂, Kinguele [00°29’N, 10°20’E], 10 km N of Kinguélé, 6 April 1986, A. Pauly (MRAC 173.087). KENYA: Western Province, 1 ♀, Kakamega forest [00°22’N, 34°50’E], alt. 1600 m, secondary forest canopy fogging of Heinsia diervilleoides, 17 January 2003, W. Freund (ZFMK AR 137); 1 ♀, same locality, canopy fogging Teclea nobilis, 7–11 February 1999, T. Wagner (ZFMK AR 1297). LIBERIA: Gbarpolu County, 1 ♀, Banga [07°16’N, 10°03’W], 26 October 1926, R.P. Strong & G.M. Allen (MCZ). RWANDA: Est Province, 1 ♀, Ibanda Makera, Rusumo [02°09’S, 30°55’E], alt. 1450 m, gallery forest canopy fogging of T. nobilis, October 1993, T. Wagner (ZFMK AR 1303). TANZANIA: Kilimanjaro Region, 1 ♀, Kibongoto [03°10’S, 37°06’E] (MNHG). UGANDA: Masindi District: 1 ♂, 1 ♀, Budongo forest [01°45’N, 31°25’E], alt. 1200 m, secondary canopy fogging of Cynometra alexandri, 15–25 January 1997, T. Wagner (ZFMK AR 1298, 1302); 1 ♂, same locality, 21–31 July 1995, T. Wagner (ZFMK AR 1300); 1 ♂, same locality, primary forest canopy fogging of Rinorea beniensis, 19–30 June 1995, T. Wagner (ZFMK AR 1301); 1 ♂, same locality, swamp forest canopy fogging of T. nobilis, 1–10 July 1995, T. Wagner (ZFMK AR 1299). Etymology. Named after the husband of the first author, Eduard Stakesby. Noun in genitive gender. Diagnosis. Females may be recognised by carapace that is often decorated with darker brown patch centrally, laterally and/or posteriorly (Fig. 38); epigyne with narrow, curved hood anteriorly, differs from M. soleil n. sp. that have a wider hood; intromittent orifices two circular openings, antero-laterally (Fig. 85), intromittent orifices as in Fig. 86. Male palp with RTA fairly broad at base, tip curving gradually laterally, situated close to bulb (Figs 83, 84). Description. Female. Size, measurements (n = 6). TL: 3.15 (2.72–4.07); CL: 1.22 (1.06–1.39); CW: 1.10 (0.99–1.30); CI: 1.11(1.06–1.20); CH: 0.74 (0.63–0.88); CLL: 0.21 (0.16–0.25); MOQ-L: 0.25 (0.21–0.28). Colour. Carapace dorsally varies from dark copper-red, orange to brown; usually with dark brown central band or patch which may extend from eye area or clypeus posteriorly; laterally with paler orange-brown to yellow areas; abdomen paler than carapace, unevenly brownish to pale, with faint white border, may be decorated with pale, purple-grey or dark brown triangular patterns; ventrally pale with dark brown striae; all legs yellow-orange, with brown band partially present over width of femora I-IV. Carapace. With fine granules or small holes; few long, erectile setae on postero- or postero-lateral edge and laterally of LE. Sternum. Slightly longer than wide; SL: 0.54; SW: 0.50; SI: 1.09. Eyes. Eye measurements: AME–AME: 0.23; ALE–AME: 0.33; AME–AME/AME–ALE: 0.69; PME–PME: 0.36; PLE–PME: 0.32; PME–PME/PME–PLE: 1.13; ALE/AME: 1.46; PLE/PME: 0.89; MOQ–AW/ MOQ-PW: 0.63; MOQ-L/MOQ-W: 0.39; Clyp/AME– AME: 0.92. Legs. Long and slender; femora, patellae and tibiae I–IV with few medium spiniform setae dorsally and laterally; tibiae with long and short spiniform setae; metatarsi and tarsi III–IV with numerous fine setae and small spiniform setae, also present ventrally on tibiae I–IV and latero-dorsally on metatarsi I–IV; leg formula: II:I:IV:III; leg measurements: leg I—Fe 0.91, Pat 0.32, Tib 0.74, Mt 0.58, Ta 0.44, total 2.99; II—Fe 1.00, Pat 0.35, Tib 0.73, Mt 0.60, Ta 0.44, total 3.12; III—Fe 0.64, Pat 0.28, Tib 0.46, Mt 0.36, Ta 0.30, total 2.05; IV—Fe 0.74, Pat 0.29, Tib 0.57, Mt 0.41, Ta 0.29, total 2.30. Abdomen. Round. AL: 1.93; AW: 1.73; AI: 1.12. Epigyne. With well-defined, small hood centrally and narrow atrium (Fig. 85) small circular intromittent orifices situated laterad of hood; intromittent canals as in Fig. 86. Male. Size, measurements (n = 3). TL: 2.50 (2.34–2.76); CL: 1.12 (1.03–1.20); CW: 0.98 (0.90–1.40); CI: 1.15 (1.14–1.15); CH: 0.66 (0.54–0.72); CLL: 0.19 (0.18–0.22); MOQ-L: 0.23 (0.23–0.24). Similar to female but differs as follows: body smaller and more slender. Colour. Carapace uniform dark copper-red (Fig. 39); abdomen slightly paler brown with faint black tinted marks; femora I–IV, tibiae and metatarsi IV with partially copper or brown tint. Carapace. With fewer long setae. Sternum. SL: 0.49 SW: 0.48 SI: 1.02. Eyes. ALE large; PME equally close to PLE than to each other; eye measurements: AME–AME: 0.20; ALE–AME: 0.28; AME–AME/AME–ALE: 0.70; PME–PME: 0.31; PLE–PME: 0.30; PME–PME/PME–PLE: 1.01; ALE/AME: 1.43; PLE/PME: 0.99; MOQ-AW/ MOQ-PW: 0.64; MOQ-L/MOQ-W: 0.37; Clyp/AME–AME: 0.99. Legs. Spiniform setae longer than in female, with short, fine, dense setae scattered in between, all leg segments with spiniform setae dorso-laterally and ventrally on metatarsi and tarsi; leg formula: I:II:IV:III; leg measurements: leg I—Fe 1.90, Pat 0.30, Tib 0.92, Mt 0.76, Ta 0.41, total 3.28; II—Fe 0.99, Pat 0.37, Tib 0.77, Mt 0.50, Ta 0.33, total 2.97; III—Fe 0.62, Pat 0.23, Tib 0.54, Mt 0.42, Ta 0.30, total 2.12; IV—Fe 0.70, Pat 0.21, Tib 0.57, Mt 0.44, Ta 0.31, total 2.22. Abdomen. Longer than wide; scutum narrow oval; AL: 1.38; AW: 0.95; AI: 1.45. Palp. With cymbial apophysis, retro-laterally (Fig. 83); VTA nearly equal in length to RTA (Fig. 84); bulb differ from M. soleil sp. n. in that the tegulum of M. stakesbyi sp. n. is not as darkly sclerotized and bulb not as wide apically as in M. soleil sp. n. Natural history. Sampled material suggest that the following tree species are preferred, Heinsia diervilleoides, Teclea nobilis, Cynometra alexandri and Rinorea beniensis in swamp, primary-, secondary- and gallery rainforests as well as some individuls were found among leaf litter. Most individuals were obtained by means of canopy fogging. Adults were sampled from October to July. Distribution. Democratic Republic of Congo (DRC), Liberia, Gabon, Ghana, Kenya, Rwanda, Tanzania and Uganda (Fig. 126)., Published as part of Honiball Lewis, Allet S. & Dippenaar-Schoeman, Ansie S., 2014, Revision of the spider genus Mystaria Simon, 1895 (Araneae: Thomisidae) and the description of a new genus from the Afrotropical region, pp. 101-144 in Zootaxa 3873 (2) on pages 131-132, DOI: 10.11646/zootaxa.3873.2.1, http://zenodo.org/record/4948115
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39. Mystaria mnyama Honiball Lewis & Dippenaar-Schoeman 2014, sp. n
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Honiball Lewis, Allet S. and Dippenaar-Schoeman, Ansie S.
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Mystaria mnyama ,Arthropoda ,Mystaria ,Arachnida ,Animalia ,Araneae ,Biodiversity ,Thomisidae ,Taxonomy - Abstract
Mystaria mnyama sp. n. Figs 23–25, 61–64, 120 Type material: Holotype: ♀, SOUTH AFRICA: KwaZulu-Natal Province, Tembe Elephant Park, sparse woodland, sweeping grasses [26°52’S, 32°27’E], 7 July 2007, C. Haddad (NCA 2008/2839). Paratype: 1 ♂, Tembe Elephant Park [27°03’S, 32°24’E], open woodland, beating short shrubs, 7 July 2007, C. Haddad (NCA 2008/2822). Etymology. ‘Mnyama’ means black in Zulu, as this species is recognised by the black-tinted areas on the cephalic and eye area. The name is to be treated as a noun in apposition. Diagnosis. Females can be recognised by the distinct colour patterns on body (Fig. 23); epigyne with atrium bullet-shaped and small notch anteriorly (Fig. 63). Male is very dark with pale legs (Fig. 25); bulb with sturdy RTA (Fig. 62); RTA with long tip directed antero-laterally, tutaculum present retro-laterally (Fig. 61). Description. Female. Size, measurements (n = 1). TL: 2.64; CL: 1.06; CW: 0.94; CI: 1.13; CH: 0.73; CLL: 0.23; MOQ-L: 0.24. Colour. Carapace copper-red, black tint in eye region and postero-lateral side of carapace (Fig. 23, 24); clypeus with orange patch; sternum dark; abdomen dorsally very pale with two dark spots laterally; ventrally blue tint with metallic purplish-blue to pinkish-brown striae; legs uniform yellow with femora I–II a darker orange (Fig. 24). Carapace. Slightly granular. Sternum. SL: 0.43; SW: 0.46; SI: 0.95. Eye s. AME large; eye measurements: AME–AME: 0.22; ALE–AME: 0.29; AME–AME/AME–ALE: 0.75; PME–PME: 0.34; PLE–PME: 0.26; PME–PME/PME–PLE: 1.27; ALE/AME: 1.33; PLE/PME: 0.79; MOQ-AW/PW: 0.64; MOQ-L/ MOQ-W: 0.37; Clyp/AME–AME: 1.06. Legs. All legs with medium-length setae; spiniform setae present on the following leg segments: on femora I–III three short, thick setae; tibiae I–IV with at least three setae; tibiae III–IV dorsally and ventrally with setae; leg formula: I:II:IV:III; leg measurements: leg I—Fe 0.74, Pat 0.29, Tib 0.64, Mt 0.52, Ta 0.40, total 2.58; II—Fe 0.76, Pat 0.29, Tib 0.61, Mt 0.50, Ta 0.37, total 2.53; III—Fe 0.50, Pat 0.20, Tib 0.40, Mt 0.30, Ta 0.24, total 1.64; IV—Fe 0.60, Pat 0.23, Tib 0.49, Mt 0.41, Ta 0.29, total 2.02. Abdomen. AL: 1.58; AW: 1.58; AI: 1.00. Epigyne. Atrium small, bullet-shaped, small notch anteriorly (Fig. 63); intromittent orifices small, open antero-laterally; intromittent canals as in (Fig. 64). Male. Size, measurements (n = 1). TL: 2.29; CL: 0.97; CW: 0.88; CI: 1.11; CH: 0.66; CLL: 0.22; MOQ-L: 0.22. Differ from female as follows: Colour. Body dark blackish to copper with a white border in anterior half of abdomen; ventrally greyish to brownish-purple striae; legs uniformly pale-yellow in contrast to body (Fig. 25). Carapace. Round. Sternum. SL: 0.40 SW: 0.44 SI: 0.89. Eyes. Eye measurements: AME–AME: 0.20; ALE–AME: 0.28; AME–AME/AME–ALE: 0.74; PME–PME: 0.31; PLE–PME: 0.23; PME–PME/PME–PLE: 1.37; ALE/ AME: 1.35; PLE/PME: 0.73; MOQ-AW/MOQ-PW: 0.65; MOQ-L/MOQ-W: 0.33; Clyp/AME–AME: 1.06. Legs. With dense short to medium setae on all segments; femora I–III with three spiniform setae; patella and tibiae I–IV with fairly long, thick and erectile spiniform setae; leg formula: II:I:III (leg IV damaged); leg measurements: leg I—Fe 0.77, Pat 0.25, Tib 0.68, Mt 0.55, Ta 0.42, total 2.68; II—Fe 0.84, Pat 0.26, Tib 0.76, Mt 0.55, Ta 0.42, total 2.83; III—Fe 0.52, Pat 0.23, Tib 0.46, Mt 0.31, Ta 0.29, total 1.80; IV—Fe 0.60. Abdomen. Round, anteriorly straight border, posteriorly slightly pointed; scutum with fine setae; AL: 1.32; AW: 1.18; AI: 1.12. Palp. With RTA longer than VTA, with sharp blackened tip (Fig. 61, 62). Natural history. Sampled from sweeping and beating vegetation in open woodlands of Tembe Elephant Park. Known from only two adults sampled in July, during Winter. Distribution. South Africa (KwaZulu-Natal Province) (Fig. 120)., Published as part of Honiball Lewis, Allet S. & Dippenaar-Schoeman, Ansie S., 2014, Revision of the spider genus Mystaria Simon, 1895 (Araneae: Thomisidae) and the description of a new genus from the Afrotropical region, pp. 101-144 in Zootaxa 3873 (2) on pages 122-123, DOI: 10.11646/zootaxa.3873.2.1, http://zenodo.org/record/4948115
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40. Mystaria flavogutatta Honiball Lewis & Dippenaar-Schoeman 2014, comb. n
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Honiball Lewis, Allet S. and Dippenaar-Schoeman, Ansie S.
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Mystaria flavogutatta ,Arthropoda ,Mystaria ,Arachnida ,Animalia ,Araneae ,Biodiversity ,Thomisidae ,Taxonomy - Abstract
Mystaria flavogutatta (Lawrence, 1952) comb. n. Figs 2, 11–13, 45–48, 116 Paramystaria flavoguttata Lawrence 1952: 14; fig. 8 (descr. juvenile ♀). Jézéquel 1964: 1111. Type material: Holotype (designated by Lawrence 1952): juvenile ♀, DEMOCRATIC REPUBLIC OF CONGO (DRC): Katanga Region, Grotte de Kakontwe [10°59’S, 26°40’E] found at entrance of cave beneath stones, 3 August 1948, N. Leleup (MRAC 81211, examined). Other material examined. SOUTH AFRICA: Eastern Cape Province, sub-adult ♂, juvenile ♀, Cwebe Nature Reserve, The Haven [31°45’S, 29°16’E], beating of coastal dune forest, 30 October 2006, R. Lyle & C. Haddad (NCA 2007/332). KwaZulu-Natal Province, 1 ♀, Ndumo Game Reserve [26°54’S 32°15’E], Malaise traps in sand forest and broad leaf deciduous forest, 4–8 December 2009, A.H. Kirk-Spriggs (NMBA); 1 ♀, Richards Bay [28°47’S, 32°06’E], tree beating, 26 April 2004, T. Wassenaar (NCA 2009/5037). Limpopo Province, 1 ♂, Kruger National Park, Punda Maria Camp, Shipudze [22°27’S, 31°13’E], 19 December 1962, R.F. Lawrence (NM 23345). SWAZILAND: Hhohho Region, juvenile ♀, Piggs Peak area, Hhlehhlele [25°50’S, 31°13’E], handpicked outside pit-toilet, at foot of mountain, 29 October 2011, A.S. Lewis (NCA 2012/325). Diagnosis. Both sexes recognised by carapace with highly elevated thoracic region; in female usually with pattern (Fig. 12) or in holotype juvenile female abdomen uniform in colour with two prominent spots posteriorly. Femora I–IV with numerous short setae ventrally. Female epigyne with atrium well-defined cube-shape (Fig. 47), intromittent canals as in Fig. 48. Male palp with VTA finger-shaped, RTA tooth-like (Fig. 45) extending laterally with a slight curve (Fig. 46) and a small cymbial apophysis. Re-description. Female. Size, measurements (n = 1). TL: 4.58; CL: 1.53; CW: 1.41; CI: 1.08; CH: 1.18; CLL: 0.24; MOQ-L: 0.31. Colour. Carapace and legs copper-brown to orange-yellow; leg III sometimes paler; abdomen pale copper, may resemble M. rufolimbata in both having two contrasting spots postero-dorsally; two spots may either be circles, or form contrasting border encircling abdomen (Fig. 12). Chelicerae. As in Fig. 2. Sternum. SL: 0.59 SW: 0.75 SI: 0.78. Eyes. PME fairly small; eye measurements: AME–AME: 0.29; ALE–AME: 0.35; AME–AME/AME–ALE: 0.83; PME–PME: 0.41; PLE–PME: 0.33; PME–PME/PME–PLE: 1.25; ALE/AME: 1.20; PLE/PME: 0.80; MOQ-AW/MOQ-PW: 0.71; MOQ-L/MOQ-W: 0.43; CLYP/AME–AME: 0.80. Legs. Two to three spiniform setae in a row, present on tibiae directed latero-ventrally to leg and dorsally on tibiae and patellae; leg formula: II:I:IV:III; leg measurements: leg I—Fe 0.87, Pat 0.33, Tib 0.94, Mt 0.73, Ta 0.54, total 3.41; II—Fe 1.01, Pat 0.38, Tib 0.99, Mt 0.78, Ta 0.61, total 3.76; III—Fe 0.71, Pat 0.33, Tib 0.63, Mt 0.47, Ta 0.38, total 2.51; IV—Fe 0.89, Pat 0.35, Tib 0.73, Mt 0.54, Ta 0.40, total 2.91. Abdomen: AL: 3.06; AW: 2.59; AI: 1.18. Epigyne. Atrium well-defined cube-shaped; intromittent orifices open laterally (Fig. 47); intromittent canals complex (Fig. 48); spermathecae small, situated postero-laterally. Male. Size, measurements (n = 1). TL: 3.43; CL: 1.36; CW: 1.36; CI: 1.00; CH: 0.96; CLL: 0.32; MOQ-L: 0.28. Resemble females but differs as follows: Colour. Carapace uniform reddish-brown; abdomen orange to copper. Legs uniform in colour, leg III sometimes paler. Carapace. With denser setae. Clypeu s. With long and numerous setae on edge. Sternum. SL: 0.59; SW: 0.67; SI: 0.88. Eye s. Eye measurements: AME–AME: 0.28; ALE–AME: 0.32; AME–AME/AME–ALE: 0.89; PME–PME: 0.40; PLE–PME: 0.35; PME–PME/PME–PLE: 1.13; ALE/AME: 1.13; PLE/PME: 0.88; AME–AME/AME–ALE: 0.89; PME–PME/PME–PLE: 1.13; MOQ-AW/ MOQ-PW: 0.71; MOQ-L/MOQ-W: 0.40; CLYP/AME–AME: 1.13. Legs. Leg formula: I:II:IV:III; leg measurements: leg I—Fe 1.08, Pat 0.35, Tib 0.94, Mt 0.73, Ta 0.56, total 3.67; II—Fe 1.13, Pat 0.38, Tib 0.89, Mt 0.68, Ta 0.56, total 3.64; III—Fe 0.75, Pat 0.31, Tib 0.59, Mt 0.45, Ta 0.35, total 2.44; IV—Fe 0.87, Pat 0.31, Tib 0.63, Mt 0.49, Ta 0.38, total 2.68; Abdomen. AL: 2.07: AW: 1.81; AI: 1.14. Palp (only left palp available). Embolus long, thin, coiling at least twice around bulb (Fig. 45); RTA broad at base, tip sharply pointed; VTA finger-shaped (Fig. 46). Natural history. Sampled from trees in savanna and coastal forest habitats. The holotype was found under a stone at a cave entrance. Adults were sampled from December to April and juveniles in October. Distribution. Democratic Republic of Congo (DRC). New record: South Africa (Fig. 116)., Published as part of Honiball Lewis, Allet S. & Dippenaar-Schoeman, Ansie S., 2014, Revision of the spider genus Mystaria Simon, 1895 (Araneae: Thomisidae) and the description of a new genus from the Afrotropical region, pp. 101-144 in Zootaxa 3873 (2) on pages 118-119, DOI: 10.11646/zootaxa.3873.2.1, http://zenodo.org/record/4948115, {"references":["Lawrence, R. F. (1952) A collection of cavernicolous and termitophilous Arachnida from the Belgian Congo. Revue de zoologie et de botanique africaines, 46, 1 - 17.","Jezequel, J. F. (1964) Araignees de la savane de Singrobo (Cote d'Ivoire). III. - Thomisidae. Bulletin de l Institut francais de Afrique Noire, 26, 1103 - 1143."]}
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41. Mystaria occidentalis Honiball Lewis & Dippenaar-Schoeman 2014, comb. n
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Honiball Lewis, Allet S. and Dippenaar-Schoeman, Ansie S.
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Mystaria occidentalis ,Arthropoda ,Mystaria ,Arachnida ,Animalia ,Araneae ,Biodiversity ,Thomisidae ,Taxonomy - Abstract
Mystaria occidentalis (Millot, 1942) comb. n. Figs 26–28, 65–68, 121 Paramystaria variabilis occidentalis Millot 1942: 8, fig. 3 (descr. ♀). Type material: Lectotype (by present designation): ♀, REPUBLIC OF GUINEA: Mamou Region, Kouroussa [11°15’N, 11°59’W], August 1937, J. Millot (MNHN) (material not well-preserved, bleached). Syntype series from MNHN was examined. A female from the syntype series is elected as a new lectotype. Paralectotypes: 2 ♀, same data as lectotype (MNHN) Other material examined. CAMEROON: Adamawa Region, 1 ♂, Chabal Mbabo [07°25’N, 12°49’E], alt 1250 m, SW-slope, 7–13 April 1983, R. Bosmans & J. Van Stalle (MRAC 162.638); 1 ♂, 1 juvenile ♀, Mbam mountain near Koutoupi [07°25’N, 12°49’E], W-slope alt. 1100 m, Ndop plateau, forest litter, sweeping, 31 March 1983, R. Bosmans & J. Van Stalle (MRAC 162.645). East Region, 1 juvenile, Letta [04°55’N, 13°51’E], alt. 1100 m, 50 km N of Bertoua, sweeping, 3 March 1983, R. Bosmans & J. Van Stalle (MRAC 162.732). DEMOCRATIC REPUBLIC OF CONGO (DRC): Katanga Region, 1 ♀, Likasi (Jadotville), 11.2 km NW [10°59’S, 26°44’E], alt 1350 m, 27 January 1958, E.S. Ross & R.E. Leech (CAS). Nord-Kivu Region, 1 ♀, 1 ♂, Ishanga spillway of Lake Edward into Semliki [00°08’S, 29°36’E], 26–29 December 1968, R.P.M. Lejeune (MRAC 135.362, 135.368); 2 ♀, Semliki middle valley [01°13’N, 30°32’E], sweeping, 8 August 1968, R.P.M. Lejeune (MRAC 135.463, 135.439); 6 ♀, 5 ♂, Lulimbi, river mouth Ishasha into Lake Edward, SE [00°32’S, 29°40’E], gallery forest beating dense shrub, July–August 1976, R.P.M. Lejeune (MRAC 168.314, 169.056, 169.031); 1 ♂, same locality, sweeping meadow, July–August 1976 (MRAC 169.079); 1 ♀, Sake [01°34’S, 29°02’E], March 1936, L. Lippens (MRAC 20737); 1 ♀, N’Zulu, Lake Kivu [01°37’S, 29°06’E], 13–14 February 1934, G.F. De Witt (MRAC 222219). Orientale Region, 3 ♀, Kivu, valley of Kaisola, Plain of Ruindi [00°47’S, 29°17’E], beating, alt. 1100 m, 3 July 1972, R.P.M. Lejeune (MRAC 144.494, 144.595). Sud-Kivu Region, 1 ♀, Bukavu [02°27’S, 28°43’E], December 1954, H. Bomans (MRAC 85564). MOZAMBIQUE: Tete Province, 1 ♀, 1 ♂, Tete [16°09’S, 33°34’E], April 1947 (SMF 9976, 10-034); 1 ♀, Ponta Torres, Inhaca Island [26°00’S, 32°56’E], coastal beach forest, 22 December 1992, T. Steyn (NCA 93/240). RWANDA: Est Province, 1 ♀, Gabiro [01°31’S, 30°28’E], November 1985, R. Jocqué, J. Nsengimana & J.P Michiels (MRAC 165.867); 1 ♀, PN. Akagera, Lake Ihema, fisheries [01°55’S, 30°45’E], sweeping, alt. 1298 m, 8 December 1985, R. Jocqué, J. Nsengimana & J.P. Michiels (MRAC 165.830); 2 ♂, 2 ♀, same locality, beating on three tree spp. Acacia, Ziziphus and Commiphora, 1 July–29 November 1985, R. Jocqué, J. Nsengimana & J.P. Michiels (MRAC 165.370, 165.460); 1 ♀, same locality, 6 km south of fisheries [01°40’S, 30°35’E], dry forest, 5 December 1985, R. Jocqué, J. Nsengimana & J.P. Micheils (MRAC 165.670). Sud Province, 1 ♂, Butare [02°36’S, 29°43’E], April 1968, E. Vertriest (MRAC 134.811). SOUTH AFRICA: KwaZulu-Natal Province, 1♂, 1 ♀, Mtunzini, Twin Streams Farm [28°57’S, 31°46’E], 15 December 1963, W. Lawson & O. Bourquin (NM); 1 ♀, Hellsgate [28°07’S, 32°18’E], blue traps, tsetse fly survey, 15 February 2004, J. Esterhuizen (NCA 2009/4613); 1 ♀, 1 juvenile, Umtamvuna Nature Reserve [32°11’S, 28°58’E], L. Berio (MNHG). TANZANIA: Morogoro Province, 1 ♀, Tanganyika territory [09°06’S, 35°38’E], October 1926, A. Loveridge (MCZ). UGANDA: Jinja District, 1 ♀, Busaga district, Mount Kisunyi [00°40’N, 33°18’E], February 1967, T.Ruabunesa (MRAC 131.591). Kampala Disctrict, 3 ♂, 1 ♀, sub-adult ♂ Rubaga [00°18’N, 32°33’E], sweeping, April –August 1994, D. Penney (MRAC 210194, 210216, 210206); 1 ♂, 3 ♀, same locality, found on flowers, 6 August 1994, D. Penney (MRAC 210192). Remarks. Millot (1942) described Paramystaria variabilis occidentalis as a subspecies of P. variabilis, based mainly on colour variation. A critical examination of P. v. occidentalis revealed that the epigyne differs from that of P. variabilis and these differences necessitate the recognition of P. occidentalis as a distinct species within Mystaria. Diagnosis. Females recognised by colour patterns on body (Fig. 26); differ from other species which may have similar abdominal patterns by slightly larger lateral eyes which are situated closer to PME; epigyne with atrium rim teardrop-shaped, small flap posteriorly; small intromittent orifices open antero-laterally (Fig. 67). Male dark with pale legs, femora I and II may have dark infuscated bands (Fig. 28); RTA with long slender tip directed laterally with slight curve anteriorly (Fig. 65); VTA slender (Fig. 66). Re-description. Female. Size, measurements (n = 21). TL: 2.99 (2.56–3.76); CL: 1.12 (1.05–1.33); CW: 1.01 (0.92–1.20); CI: 1.11 (1.04–1.20); CH: 0.70 (0.60–0.86); CLL: 0.22 (0.15–0.27); MOQ-L: 0.24 (0.20–0.28). Colour. Carapace varies from dark copper-brown to orange-red, colour and patterns vary between individuals, may be uniform in colour or tinted darker on certain areas: usually with two darker bands dorso-laterally (Fig. 26) or darker areas in eye region, may have two small lightly coloured triangles on postero-lateral sides and/or dark bands on thoracic area, in orange specimens carapace dark postero-laterally; clypeus and anterior eye area paler or brighter colour; chelicerae sometimes orange at base and dark distally; labium dark; sternum orange-brown or sometimes with darker brown pattern; abdomen varies: dorsally pale or with blue tint, may have a darker brown medial band or lateral patterns; ventrally striae striped; legs I–IV uniform pale yellow (Fig. 27), or femora I–II often with darker tint; tibiae, metatarsi and tarsi II or IV sometimes dark. Carapace. Smooth, not granular. Sternum. SL: 0.48; SW: 0.51; SI: 0.95. Eye s. Eye measurements: AME–AME: 0.22; ALE–AME: 0.30; AME–AME/ AME–ALE: 0.72; PME–PME: 0.35; PLE–PME: 0.28; PME–PME/PME–PLE: 1.26; ALE/AME: 1.40; PLE/PME: 0.81; MOQ-AW/MOQ-PW: 0.63; MOQ-L/MOQ-W: 0.39; Clyp/AME–AME: 1.01. Legs. Two or three small setae on femora, rest of leg segments covered densely with fine setae, few small strong setae dorsally and ventrally on patellae and tibiae; leg formula: II:I:IV:III; leg measurements: leg I—Fe 0.77, Pat 0.27, Tib 0.58, Mt 0.50, Ta 0.39, total 2.51; II—Fe 0.79, Pat 0.28, Tib 0.63, Mt 0.52, Ta 0.37, total 2.59; III—Fe 0.58, Pat 0.25, Tib 0.42, Mt 0.33, Ta 0.28, total 1.86; IV—Fe 0.67, Pat 0.25, Tib 0.50, Mt 0.43, Ta 0.31, total 2.16. Abdomen. Covered with short setae embedded in small tubercles; AL: 1.87; AW: 1.76; AI: 1.06. Epigyne. Wide posteriorly with small flap centrally, almost closed anteriorly (Fig. 67); intromittent canals complex, as in Fig. 68. Male. Size, measurements (n = 12). TL: 2.39 (2.10–2.64); CL: 1.02 (0.90–1.14); CW: 0.92 (0.80–1.00); CI: 1.11 (1.05–1.19); CH: 0.62 (0.54–0.72); CLL: 0.22 (0.18–0.24); MOQ-L: 0.22 (0.20–0.24). Resemble females but differ as follows: Colour. Body dark or rich copper-brown; abdomen dorsally with or without patterns, sometimes with narrow bluish or white border anteriorly; ventrally uniform metallic blue, pinkish-purple or pale with blue and white striped striae; legs either pale or femora I–II and tibiae, metatarsi and tarsi IV darker (Fig. 28). Sternum. SL: 0.42 SW: 0.46 SI: 0.92. Eyes. Large; eye measurements: AME–AME: 0.21; ALE–AME: 0.27; AME–AME/ AME–ALE: 0.79; PME–PME: 0.31; PLE–PME: 0.25; PME–PME/PME–PLE: 1.26; ALE/AME: 1.29; PLE/PME: 0.80; MOQ-AW/MOQ-PW: 0.68; MOQ-L/MOQ-W: 0.34; Clyp/AME–AME: 1.05. Legs. Usually with short setae; leg formula: II:I:IV:III; leg measurements: leg I—Fe 0.84, Pat 0.26, Tib 0.73, Mt 0.59, Ta 0.43, total 2.85; II—Fe 0.91, Pat 0.28, Tib 0.75, Mt 0.60, Ta 0.42, total 2.95; III—Fe 0.56, Pat 0.23, Tib 0.48, Mt 0.35, Ta 0.29, total 1.92; IV—Fe 0.64, Pat 0.32, Tib 0.52, Mt 0.44, Ta 0.31, total 2.23. Abdomen. AL: 1.36; AW: 1.17; AI: 1.17. Palp. Embolus long with at least three coils; VTA and RTA almost same length (Figs 65, 66). Natural history. Sampled from sweeping and beating vegetation such as trees shrubs and from forest litter in coastal beach forest, gallery forests, marshy areas near lakes and mountainous areas. Collected material suggested adults to be abundant from July to April whereas juveniles appeared from March to June. Distribution. Republic of Guinea. New records: Cameroon, Democratic Republic of Congo (DRC), Mozambique, Rwanda, South Africa, Tanzania and Uganda (Fig. 121).
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42. Mystaria oreadae Honiball Lewis & Dippenaar-Schoeman 2014, sp. n
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Honiball Lewis, Allet S. and Dippenaar-Schoeman, Ansie S.
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Arthropoda ,Mystaria ,Arachnida ,Mystaria oreadae ,Animalia ,Araneae ,Biodiversity ,Thomisidae ,Taxonomy - Abstract
Mystaria oreadae sp. n. Figs 29, 30, 69, 70, 95–98, 122 Type material: Holotype: ♀, RWANDA: Nord Province, Rwankuba [ 01°45’S, 29°51’E], alt. 2200 m, 23 August 1953, A.E. Bertrand (MRAC 78855). Paratypes: 2 ♀, same locality data as holotype (MRAC 78856-7). DEMOCRATIC REPUBLIC OF CONGO ( DRC): Orientale Region, 1 ♀, Ituri, Mount Bugera [00°10’S, 29°14’E], November 1953, R.P. Bergmans & R.P. Celis (MRAC 76630). Etymology. This species, which was sampled exclusively from mountainous regions is named after ‘Oread’, a mountain nymph in old Greek mythology. Noun in genitive case. Diagnosis. Females can be recognised by the colour patterns on body. Femora I–IV infuscated totally or partially with brown band (Figs 29, 30). Epigyne with atrium rim horseshoe-shaped, small hood centrally (Fig. 69). Male unknown. Description. Female. Size, measurements (n = 3). TL: 3.20 (2.74–3.53); CL: 1.14 (1.01–1.27); CW: 1.09 (0.97–1.22); CI: 1.05 (1.04–1.07); CH: 0.66 (0.63–0.70); CLL: 0.23 (0.20–0.26); MOQ-L: 0.24 (0.24–0.25). Colour. Carapace varies from red to orange copper, may be tinted darker on thoracic region with paler triangles postero-laterally or darkened on posterior edge, colour and patterns varies between individuals; chelicerae orange to copper, with tinted black tips; sternum dark copper; abdomen dorsally pale white, may have a median longitudinal band which extends to spinnerets and striae; ventrally uniformly metallic blue to turqoise or slightly dark pink; striae blue-grey; all legs segments except femora I–IV uniform orange-yellow (Fig. 30). Carapace. Slightly granular; setae present on clypeal edge and laterally of ALE and PLE. Sternum. SL: 0.48; SW: 0.53; SI: 0.91. Eye s. Eye measurements: AME–AME: 0.22; ALE–AME: 0.31; AME–AME/AME–ALE: 0.72; PME–PME: 0.37; PLE–PME: 0.28; PME–PME/PME–PLE: 1.35; ALE/AME: 1.40; PLE/PME: 0.74; MOQ-AW/MOQ-PW: 0.60; MOQ-L/MOQ-W: 0.41; Clyp/AME–AME: 1.04. Legs. Short setae present on all legs; spiniform setae present on the following segments: femora laterally with two or three medium-length setae; tibia ventrally or dorsally with many scattered, erectile and long setae; tibiae ventrally with two fairly long setae situated distally; tarsal claws as in Figs 95–98; leg formula: II:I:IV:III; leg measurements: leg I—Fe 1.75, Pat 0.30, Tib 0.59, Mt 0.50, Ta 0.40, total 2.53; II—Fe 0.75, Pat 0.30, Tib 0.62, Mt 0.50, Ta 0.40, total 2.57; III—Fe 0.58, Pat 0.26, Tib 0.43, Mt 0.34, Ta 0.29, total 1.89; IV—Fe 0.66, Pat 0.24, Tib 0.50, Mt 0.42, Ta 0.30, total 2.12. Abdomen. Slightly wider posteriorly; AL: 2.06; AW: 1.80; AI: 1.14. Epigyne. Intromittent orifices small, open antero-laterally (Fig. 69); intromittent canals visible ventrally, postero-laterally to rim; intromittent canals as in Fig. 70. Male. Unknown. Natural history. Specimens have been sampled from mountainous regions. Females were found to occur from August to November. Distribution. Rwanda and Democratic Republic of Congo (DRC) (Fig. 122)., Published as part of Honiball Lewis, Allet S. & Dippenaar-Schoeman, Ansie S., 2014, Revision of the spider genus Mystaria Simon, 1895 (Araneae: Thomisidae) and the description of a new genus from the Afrotropical region, pp. 101-144 in Zootaxa 3873 (2) on page 126, DOI: 10.11646/zootaxa.3873.2.1, http://zenodo.org/record/4948115
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43. Mystaria lindaicapensis Honiball Lewis & Dippenaar-Schoeman 2014, sp. n
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Honiball Lewis, Allet S. and Dippenaar-Schoeman, Ansie S.
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Arthropoda ,Mystaria ,Arachnida ,Animalia ,Araneae ,Mystaria lindaicapensis ,Biodiversity ,Thomisidae ,Taxonomy - Abstract
Mystaria lindaicapensis sp. n. Figs 20–22, 57–60, 119 Type material: Holotype: ♀, SOUTH AFRICA: Eastern Cape Province, Jeffreys Bay [34°02’S, 24°55’E], in garden, 15 July 2008, L. Wiese (NCA 2009/5036). Paratypes: 1 ♂, same locality data as holotype, L. Wiese (NCA 2009/5036); Western Cape Province , 1 ♂, Knysna [34°00’S, 23°20’E] beating, 7 December 1989, L.N. Lotz (NMBA 3317). Etymology. Named after Linda Wiese who collected the holotype in the Eastern Cape Province, the southernmost locality for this genus in South Africa. Adjective. Diagnosis. Females can be recognised by the distinct colour patterns on body (Figs 20, 21); epigyne with atrium well defined, rim oval to U-shaped (Fig. 59); intromittent orifices open antero-laterally, intromittent canals very long and complex (Fig. 60). In male palp, the bulb is large and round; RTA with slender tip extending dorsolaterally (Figs 57, 58). Description. Female. Size, measurements (n = 1). TL: 3.90; CL: 1.26; CW: 1.31; CI: 0.96; CH: 0.94; CLL: 0.28; MOQ-L: 0.31. Colour. Carapace brown to dark copper, clypeus with small orange area; sternum dark; abdomen dorsally pale yellow to copper-blue, a broad, black longitudinal band centrally that expands laterally; ventrally blue with brown striae; femora I–III with infuscate brown bands dorsally and ventrally; femur IV distally with brown band; patellae yellow-orange, tibiae and metatarsi greenish, tarsi pale yellow. Carapace. Texture granular and hairy. Clypeus. Sloping. Sternum. SL: 0.64; SW: 0.67; SI: 0.95. Eye s. MOQ eye area fairly wide, eye tubercles small, PLE not very big, almost equal in size to AME; ALE>PLE>AME>PME; eye measurements: AME–AME: 0.33; ALE–AME: 0.36; AME–AME/AME–ALE: 0.92; PME–PME: 0.52; PLE–PME: 0.34; PME–PME/PME–PLE: 1.54; ALE/AME: 1.09; PLE/PME: 0.65; MOQ-AW/MOQ-PW: 0.64; MOQ-L/MOQ-W: 0.49; Clyp/AME–AME: 0.84. Legs. With very dense setae; femora with two medium spiniform setae, tibiae I-IV with two short spines; leg formula: II:I:IV:III; leg measurements: leg I—Fe 0.96, Pat 0.26, Tib 0.76, Mt 0.62, Ta 0.46, total 3.06; II—Fe 0.96, Pat 0.31, Tib 0.79, Mt 0.66, Ta 0.48, total 3.20; III—Fe 0.72, Pat 0.29, Tib 0.49, Mt 0.40, Ta 0.31, total 2.21; IV—Fe 0.78, Pat 0.34, Tib 0.60, Mt 0.52, Ta 0.36, total 2.59. Abdomen. Large, round; AL: 2.64; AW: 2.76; AI: 0.96. Epigyne. Rim extending slightly antero-laterally where intromittent orifices are situated (Fig. 59); intromittent canals longer than in other species (Fig. 60). Male. Size, measurements (n = 3). TL: 2.83 (2.78–2.87); CL 1.20 (1.15–1.25); CW: 1.13 (1.12–1.14); CI: 1.06 (1.03–1.09); CH: 0.83 (0.82–0.84); CLL: 0.26 (0.25–0.26); MOQ-L: 0.28 (0.28–0.29). Differs from female as follows: Colour. Abdomen dorsally blackish-brown with slight orange-red pattern, small blue or whitish border around abdomen (Fig. 22); ventrally metallic blue, with striae slightly darker. Femora I–II dark or with infuscate dark brownish bands; femora III–IV distally slightly darker; patellae, tibiae, metatarsi and tarsi of leg IV with darker tint, remainder of leg segments yellow or orange. Carapace. Granular and/or hairy, with few long, erectile setae present on postero-thoracic edge and laterally of ALE and PLE. Sternum. SL: 0.49 SW: 0.55 SI: 0.90. Eyes. Eye measurements: AME–AME: 0.28; ALE–AME: 0.30; AME–AME/AME–ALE: 0.92; PME–PME: 0.39; PLE–PME: 0.28; PME–PME/PME–PLE: 1.38; ALE/AME: 1.09; PLE/PME: 0.72; MOQ-AW/MOQ-PW: 0.71; MOQ-L/MOQ-W: 0.40; Clyp/AME–AME: 0.93. Legs. With dense fine setae; few long spiniform setae present on femora and tibiae I–IV, those on tibia IV especially long and erectile; tibia II & III or I–IV with numerous spiniform setae present dorsally, also present ventrally; leg formula: II:I:IV:III; leg measurements: leg I—Fe 0.90, Pat 0.30, Tib 0.74, Mt 0.65, Ta 0.50, total 3.09; II—Fe 1.01, Pat 0.34, Tib 0.85, Mt 0.73, Ta 0.47, total 3.40; III—Fe 0.64, Pat 0.26, Tib 0.50, Mt 0.37, Ta 0.31, total 2.08; IV—Fe 0.77, Pat 0.27 Tib 0.58, Mt 0.47, Ta 0.36, total 2.45. Abdomen. AL: 1.63; AW: 1.48; AI: 1.10. Palp. With tegulum large and round; RTA with dark tip, situated slightly behind bulb (Fig. 57); VTA curved tip; RTA slightly longer than VTA (Fig. 58). Distribution. South Africa (Eastern Cape and Western Cape Provinces) (Fig. 119). Natural history. Sampled from vegetation in forests and garden. Adults collected between December and July., Published as part of Honiball Lewis, Allet S. & Dippenaar-Schoeman, Ansie S., 2014, Revision of the spider genus Mystaria Simon, 1895 (Araneae: Thomisidae) and the description of a new genus from the Afrotropical region, pp. 101-144 in Zootaxa 3873 (2) on pages 121-122, DOI: 10.11646/zootaxa.3873.2.1, http://zenodo.org/record/4948115
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44. Mystaria variabilis Honiball Lewis & Dippenaar-Schoeman 2014, comb. n
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Honiball Lewis, Allet S. and Dippenaar-Schoeman, Ansie S.
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Arthropoda ,Mystaria ,Arachnida ,Animalia ,Araneae ,Biodiversity ,Thomisidae ,Taxonomy ,Mystaria variabilis - Abstract
Mystaria variabilis (Lessert, 1919) comb. n. Figs 40–42, 87–90, 127 Paramystaria variabilis Lessert 1919: 103, fig. 2, 3, 4 (descr. ♂); pl.2 figs 14, 21, 27 (descr. ♀); 1925: 323; 1936: 253; 1943: 313. Type material: Holotype (designated by Lessert 1919): ♂, TANZANIA: Kilimanjaro Region, Kibongoto [03°10’S, 37°05’E] (MNHG). Type series from MNHG was examined. Other material examined. TANZANIA: Kilimanjaro Region, 2 ♀, same locality as holotype (MNHG). DEMOCRATIC REPULIC OF CONGO (DRC) : Bass-Congo Region, 2 ♂, 6 ♀, Kisantu [05°06’S, 15°05’E], 1919, R.P. Vanderyst (MNHG). Equateur Region, 1 ♀, Bokuma [0°39’S, 21°01’E], February 1925, R.P. Lootens (MRAC 81635); 1 ♀, Bokungu, Boende [00°13’S, 20°52’E], 1950, Dupuis (MRAC 67392); 1 ♀, Bamba [06°49’S, 17°18’E], January 1940, H. De Saeger (MRAC 20088). Katanga Region, 2 ♀, Kalemie (Albertville) [05°56’S, 29°12’E], 18 November 1925, D.H. Schouteden (MNHG). Nord-Kivu Region, 1 ♀, Rwankwi [01°20’S, 29°22’E], July 1951, J. Leroy (MRAC 71571); 4 ♂, 4 ♀, 2 juveniles, Butembo, valley of Musosa [00°09’N, 29°17’E], May 1967, R.P.M. Lejeune (MRAC 132.856); 5 ♂, 2 ♀, 2 juveniles, Butembo region [00°09’N, 29°17’E], September–October 1965, M.J. Celis (MRAC 130.120); 4 ♀, Rutshuru [00°36’S, 29°27’E], March 1937, J. Gherquien (MRAC 21091, 21096, 21103, 21108). Orientale Region, 2 ♀, Watsa Niangara [03°01’N, 29°31’E], L. Burgeon (MNHG); 2 ♂, 2 ♀, Kisangani (Stanleyville) [00°31’N, 25°11’E], 28 April 1928. A. Collart (MRAC 11512/11516); 2 ♀, Saki [02°31’N, 27°25’E], March 1936. L. Lippens (MRAC 20950/20951). ETHIOPIA: Shewa Province, 1 ♂, Awash river [08°25’N, 39°25’E], sweeping, November 1966, (AMNH). KENYA: Rift Valley Province, 1 ♀, Baringo Lake, [00°28’N, 35°57’E], found on dead grass, 20 December 1979, P. Reavell (NM 13347); 1 ♂, Lodwar [03°07’N, 35°35’E], 60 km W of Lake Rudolf, 16–26 August 1963, B. Patterson (MCZ). MALAWI: Northern Region, 1 ♂, Chintheche [11°49’S, 34°10’E], 1 December 1977, R. Jocqué (MRAC 153.378). MOZAMBIQUE: Sofala Region, 1 ♀, Sangadze [17°26’S, 34°51’E], May, (MNHG). RWANDA: Kigali Province, 1 ♀, no exact locality data, (SMF); 1 ♀, Kigali [01°56’S, 30°04’E], 28–31 January 1976, J. Decelle (MRAC 147.909). Eastern Province, 1 ♂, Bugesera-Kibungo [02°09’S, 30°32’E], 22.vii.1975, P. Nyalugaka (MRAC 155.506). SOUTH AFRICA: Eastern Cape Province, 1 ♀, Port Alfred [33°36’S, 26°54’E], sweeping, 30 November 1977, A.S. Dippenaar-Schoeman (NCA 88/485). UGANDA: Masaka District, 2 ♀, Rakai [00°43’S, 31°24’E], sweeping, July 1994, D. Penney (MRAC 210209). Iganga District, 1 ♀, on banks of marsh river Tabu [00°45’N, 33°30’E], February 1967, J. Ruabunesa (MRAC 131.565). Mbarara District, 1 ♀, on bank of river Lutebe [00°27’S, 30°22’E], February 1967, J. Ruabunesa (MRAC 131.552). Diagnosis. Epigyne with atrium horseshoe-shaped; (Fig. 89); intromittent canals as in Fig. 90. Bulb round with VTA broad at base; RTA thickened at base, extending straight, directed antero-laterally (Fig. 87). Re-description: Female. Size, measurements (n = 6). TL: 3.14 (3.06–3.45); CL: 1.22 (1.18–1.34); CW: 1.11 (1.12–1.22); CI: 1.10 (1.04–1.18); CH: 0.75 (0.63–0.82); CLL: 0.24 (0.18–0.27); MOQ-L: 0.25 (0.23–0.28). Colour. Carapace often with dark copper markings on thoracic, cephalic region and eye area, paler posterolaterally; uniform specimens with orange colour and postero-thoracic edge tinted; eyes on black tubercles; clypeus with yellow patch (Fig. 40); sternum brown and chelicerae uniform copper. Carapace and abdomen colour and patterns may vary between idividuals. Abdomen pale with variable pattern dorsally: a grey longitudinal band with slightly zig-zag edge, or band extending wider anteriorly and centrally; ventrally pale white with pale blue to darker grey striae; legs usually uniform pale yellow-orange, femora I–II may have infuscated brown bands; femora III–IV brown distally (Figs 40, 41). Carapace. Broad. Sternum. SL: 0.50; SW: 0.52; SI: 0.97. Eye s. Eye measurements: AME–AME: 0.22; ALE–AME: 0.30; AME–AME/AME–ALE: 0.75; PME–PME: 0.37; PLE–PME: 0.30; PME–PME/PME–PLE: 1.24; ALE/AME: 1.34; PLE/PME: 0.81; MOQ-AW/MOQ-PW: 0.61; MOQ-L/MOQ-W: 0.41; Clyp/AME–AME: 1.06. Legs. With numerous fine setae, dark erectile setae present dorsally, ventrally and laterally on all segments; tibia and femora with five long spiniform setae; leg formula: II:I:IV:III; leg measurements: leg I—Fe 0.81, Pat 0.29, Tib 0.64, Mt 0.54, Ta 0.43, total 2.71; II—Fe 0.79, Pat 0.31, Tib 0.66, Mt 0.55, Ta 0.42, total 2.72; III—Fe 0.63, Pat 0.28, Tib 0.45, Mt 0.37, Ta 0.29, total 2.01; IV—Fe 0.73, Pat 0.27, Tib 0.56, Mt 0.47, Ta 0.34, total 2.37. Abdomen. Round to slightly wider posteriorly. AL: 1.92; AW: 1.75; AI: 1.11. Epigyne. Intromittent orifices open antero-laterally; intromittent canals long and complex with large coils anteriorly on both sides (Fig. 90). Male. Size, measurements (n = 3). TL: 2.49 (2.34–2.59); CL: 1.08 (1.08–1.09); CW: 0.96 (0.90–1.01); CI: 1.13 (1.08–1.20); CH: 0.66 (0.66–0.66); CLL: 0.22 (0.21–0.24); MOQ-L: 0.23 (0.20–0.26). Differ from female as follows: Colour. Body orange or copper-red, abdomen dorsally dusted with blackish-brown pattern, usually with pale border anteriorly (Fig. 42); ventrally pale blue or slightly metallic blue, with striae darker blue; clypeus lighter yellow or orange area; legs usually uniform pale, with shades of brown or orange-yellow; femora I–II, tibiae and/or metatarsi IV may be slightly darker. Carapace. Smooth. Sternum. SL: 0.44; SW: 0.45; SI: 0.98. Eyes. Eye measurements: AME–AME: 0.19; ALE–AME: 0.28; AME–AME/AME–ALE: 0.67; PME–PME: 0.33; PLE–PME: 0.27; PME–PME/PME–PLE: 1.21; ALE/AME: 1.49; PLE/PME: 0.83; MOQ-AW/MOQ-PW: 0.56; MOQ-L/MOQ-W: 0.42; Clyp/AME–AME: 1.18. Legs. Leg segments covered with very fine medium length setae; femora and tibiae I–IV with few medium length, spiniform setae; leg formula: I:II:IV:III; leg measurements: leg I—Fe 0.91, Pat 0.26, Tib 0.78, Mt 0.61, Ta 0.31, total 2.87; II—Fe 0.61, Pat 0.19, Tib 0.53, Mt 0.41, Ta 0.29, total 2.03; III—Fe 0.65, Pat 0.26, Tib 0.49, Mt 0.22, Ta 0.20, total 1.82; IV—Fe 0.69, Pat 0.23, Tib 0.57, Mt 0.30, Ta 0.22, total 2.02. Abdomen. AL: 1.41; AW: 1.20; AI: 1.17. Palp. RTA directed antero-laterally (Fig. 87); RTA slightly shorter than VTA (Fig. 88). Natural History. Specimens were sampled from vegetation. Adults were sampled throughout the year, and juveniles were sampled from May until October. Distribution. Mozambique, South Africa, Tanzania. New records: Democratic Republic of Congo (DRC), Ethiopia, Kenya, Malawi, Rwanda, and Uganda (Fig. 127).
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45. Revision of the spider genus Mystaria Simon, 1895 (Araneae: Thomisidae) and the description of a new genus from the Afrotropical region
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Honiball Lewis, Allet S. and Dippenaar-Schoeman, Ansie S.
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Arthropoda ,Arachnida ,Animalia ,Araneae ,Biodiversity ,Thomisidae ,Taxonomy - Abstract
Honiball Lewis, Allet S., Dippenaar-Schoeman, Ansie S. (2014): Revision of the spider genus Mystaria Simon, 1895 (Araneae: Thomisidae) and the description of a new genus from the Afrotropical region. Zootaxa 3873 (2): 101-144, DOI: http://dx.doi.org/10.11646/zootaxa.3873.2.1
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46. Mystaria Simon 1895
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Honiball Lewis, Allet S. and Dippenaar-Schoeman, Ansie S.
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Arthropoda ,Mystaria ,Arachnida ,Animalia ,Araneae ,Biodiversity ,Thomisidae ,Taxonomy - Abstract
Genus Mystaria Simon, 1895 Mystaria Simon 1895: 989; type species by original designation: Mystaria rufolimbata Simon, 1895. Jézéquel 1964: 1111; Ono 1988: 32. Paramystaria Lessert 1919: 102 (syn. n.); type species by original designation: Paramystaria variabilis Lessert, 1919. Diagnosis. Small spiders, body and/or legs usually decorated with spots or bands (Figs 12, 15, 21, 36). Median eyes equal in size, smaller than laterals, with MOQ area narrower in front. MOQ length only slightly shorter or longer than clypeal length. Chelicerae equipped with three small teeth (Figs 1–5). Epigyne rim simple with simple outlines (Figs 51, 59, 73, 81), intromittent canals with numerous complex coils (Fig. 74). Male with simple bulb, disc-shaped tegulum, long coiling embolus, tibia with VTA curved at tip and delicate RTA (Figs 71, 72, 87, 88). Re-description. Body length 2.1–3.3 in males, 1.90–5.24 in females. Colour. Carapace at times with patches or bands, may differ between individuals within a species or in case of males usually uniform. May have dark patches over eye region or a yellow patch on clypeus and AME area (Figs 20, 33, 40); abdomen usually with varying patterns or often uniform in case of males. Colours and bands on legs differ between species. Carapace. Circular to cube-shaped viewed from above, elevated in thoracic and sometimes cephalic region, truncated posteriorly, sloping slightly anteriorly (Figs 11, 12); smooth without setae to fairly dense covering of fine setae, usually more dense in cephalic region and on clypeus, sometimes with longer erectile setae on postero-thoracic and postero-lateral region, and around lateral eyes (Figs 38, 39). Clypeus. Vertical with or without long setae. Chelicerae. Three cheliceral teeth present, two on promargin and one on retromargin (Figs 1–5), with incurving serrated setae at tip on dorsal margin of chelicerae. Mouth parts. Labium triangular, usually longer than wide, endites converged and indented with scopula hairs on edge. Sternum. Heart-shaped, usually wider than long, anterior edge straight; posterior tip not extending beyond coxae IV; edge bordered. Eyes. AER recurved; AMELegs. Long and slender, with second pair usually longest in females, leg formula: II:I:IV:III, males with first pair of legs usually longest, leg formula: I:II:IV:III, long to medium length setae present; usually two spiniform setae ventrally on tibiae and metatarsi, distally on all legs; scopula hairs denser on leg III and IV; trichobothria present in a row on all legs; two dentated tarsal claws (Figs 91–114) with a well-defined, thick base in females, less defined base in males, with approx. 12 long slender teeth present on all tarsal claws, fewer and shorter in males with the second tooth usually on legs III & IV or II modified (flattened or broadened). Abdomen. Round to oval, bearing numerous short setae; dorsally with seven sigillae grouped in arrow-shaped formation (Fig. 17), ventrally with small sigillae in two rows; striae present ventrally around abdomen edge and dorsally of spinnerets, males with scutum, rarely with bright patterns on body (Figs 10, 13, 16). Spinnerets. Small and conical, with numerous short setae; anterior pair largest. Epigyne. Simple or delicate rim (Fig. 47, 67, 77) and atrium with (Fig. 85) or without hood, intromittent orifices open laterally or antero-laterally on atrium; intromittent canals long and extended then curving back, forming numerous complex coils, shape usually differs slightly on both sides; spermathecae small, round, situated posteriorly; fertilisation tubes short. Palp. Tibia bearing long setae; bulb round, often with tutaculum (Figs 8, 61); embolus thin (Fig. 45) or thick, of medium to long length (Fig. 43), coiling approx. three times around bulb; RTA sometimes broad at base (Fig. 75), proximally tooth-like and slender (Figs 49, 53), to broad (Figs 43, 45) or long and slender, extending far beyond the tutaclum (Figs 61); VTA with curved tip, long almost similar length as RTA (Fig. 66). Natural history. Members of Mystaria live on vegetation such as trees, shrubs, grasses or leaf litter in a diversity of natural areas including: savanna, woodland, grassland, canopies of rainforests, forest galleries, coastal dune-, sand- and riverine forests in river banks, swamps, wetlands, estuaries, valleys and mountains. Adults are found throughout the year. Distribution. This genus is endemic to Africa and known from the Democratic Republic of Congo (DRC), Republic of Guinea, Kenya, Mozambique, Namibia, Sierra Leone, South Africa and Tanzania. New records: Botswana, Côte d’Ivoire, Ethiopia, Gabon, Ghana, Liberia, Malawi, Rwanda, Uganda, Zambia and Zimbabwe. Key to species of Mystaria 1. Females............................................................................................. 2 - Males..............................................................................................14 2. Epigyne without a hood (Fig. 51).........................................................................3 - Epigyne with a hood (Fig. 81)........................................................................... 12 3. Rim of atrium U-shaped (Fig. 59)........................................................................ 11 - Rim of atrium not U-shaped............................................................................. 4 4. Rim of atrium not teardrop-shaped, rather darkly defined with contrasting pale atrium (Figs 47, 73); abdomen usually decorated with two spots on dorso-posterior end or with contrasting border; legs of similar colour to carapace, sometimes leg III different colour....................................................................................... 5 - Atrium teardrop-shaped or elongated (Figs 51, 55, 67, 77, 89); colour of body and legs different.......................6 5. Atrium cube-shaped; fovea area with fine line of dense setae (Figs 11, 12, 47)................... M. flavogutatta comb. n. - Atrium bell-shaped; more robust spider with broad carapace and no fine line of setae in fovea region (Figs 31, 73)................................................................................................... M. rufolimbata 6. Atrium long-oval (Fig. 77); all leg segments except femora dorsally with a longitudinal stripe (Fig. 34). M. savannensis sp. n. - Atrium not as above teardrop-shaped; legs without longitudinal stripes...........................................7 7. Atrium closed anteriorly; femora dark with infuscated bands dorsoventrally; tibia IV with dark band (Figs 17, 18, 55)............................................................................................... M. lata comb. n. - Rim of atrium not closed anteriorly; legs of uniform colour or with a brown band on femora.......................... 8 8. Atrium elongate; metatarsi IV and sometimes tarsi dark (Figs 15, 51)............................... M. irmatrix sp. n. - Atrium posteriorly wide; tarsi and metatarsi not dark.......................................................... 9 9. Atrium almost horseshoe-shaped (Fig. 89)................................................. M. variabilis comb. n. - Atrium more triangular (Fig. 67)....................................................... M. occidentalis comb. n. 11. Atrium quadrangular with an anterior small notch (Fig. 63)...................................... M. mnyama sp. n. - Atrium U-shaped (Fig. 59)............................................................ M. lindaicapensis sp. n. 12. Atrium horseshoe-shaped, rim with small hood centrally (Fig. 69).................................. M. oreadae sp. n. - Atrium rim different, hood situated anteriorly, at distance from posterior rim......................................13 13. Epigyne with hood wide; atrium two half circles posteriorly to hood (Fig. 81).......................... M. soleil sp. n. - Hood narrow; atrium elongate, posteriorly to hood (Fig. 85)...................................... M. stakesbyi sp. n. 14. Males with anterior legs nearly twice the length of posterior legs; central area of body covered by an orange-yellow median band, a copper-brown median band or is uniformly brown; long, erectile setae present on carapace (Figs 10, 37, 39).......15 - Posterior legs only slightly shorter than anterior legs; body is uniformly copper brown or darker coloured, may have light patterns on abdomen; carapace sometimes with setae.......................................................... 17 15. Carapace pear-shaped, narrow anteriorly, distinct spiniform setae on legs, lateral eyes large (Fig. 10), bulb elongate and hairy (Fig 43); embolus long and very well-defined (Fig 44); RTA proximally blackened, and finger-like....... M. budongo sp. n. - Carapace shape and eyes not as above; bulb apically widened (Figs 79, 83); embolus long, less-defined; RTA proximally finger-like, at an angle (Figs 80, 84)......................................................................... 16 16. Palp with VTA shorter or equal in length to RTA; carapace uniform brown as in Figs 39, 83, 84......... M. stakesbyi sp. n. - Palp with VTA longer than RTA; carapace yellow with brown median band on cephalic area, palp as in Figs 37, 79, 80............................................................................................... M. soleil sp. n. 17. All eight legs with longitudinal dorsal stripes over all segments starting at the patella of the leg (Fig. 34); palp as in Figs 75, 76..................................................................................... M. savannensis sp. n. - Legs uniform or with bands on certain segments of legs...................................................... 18 18. Carapace granular and hairy............................................................................ 19 - Carapace fairly smooth................................................................................ 21 19. Carapace with long setae on postero-thoracic edge and/or next to lateral eyes.................................... 20 - Carapace without setae on postero-thoracic edge; palp as in Figs 57, 58....................... M. lindaicapensis sp. n. 20. RTA finger-like, protruding from cymbium, palp as in Figs 45, 46............................ M. flavogutatta comb. n. - RTA with spine-like tip, in contact with cymbium, palp as in Figs 71, 72............................. M. rufolimbata 21. Legs uniformly pale in colour, in sharp contrast to body (Fig. 25) with RTA very long, blackened, extending beyond the tutaculum of the palp, as in Figs. 61, 62......................................................... M. mnyama sp. n. - Leg segments may be tinted, RTA not extending beyond the tutaculum..........................................22 22. Legs with black bands only on the metatarsi and tarsi of leg IV, palp as in Figs 49, 50................ M. irmatrix comb. n - Legs usually with bands on femora of leg I and tibia and metatarsi of leg IV...................................... 23 23. Legs with black infuscated bands dorso-ventrally on femora I, II, IV and tibia and metatarsi of leg IV; palp as in Figs 53, 54......................................................................................... M. lata comb. n. - Legs with only light brown markings....................................................................24 24. Tip of RTA bent retrolateral-dorsad (Figs 65, 66)......................................... M. occidentalis comb. n. - Tip of RTA sharp, straight (Figs 87, 88)................................................... M. variabilis comb. n., Published as part of Honiball Lewis, Allet S. & Dippenaar-Schoeman, Ansie S., 2014, Revision of the spider genus Mystaria Simon, 1895 (Araneae: Thomisidae) and the description of a new genus from the Afrotropical region, pp. 101-144 in Zootaxa 3873 (2) on pages 107-108, DOI: 10.11646/zootaxa.3873.2.1, http://zenodo.org/record/4948115, {"references":["Simon, E. (1895) Histoire naturelle des Araignees. Vol. 1. Roret, Paris, 1084 pp. http: // dx. doi. org / 10.5962 / bhl. title. 51973","Jezequel, J. F. (1964) Araignees de la savane de Singrobo (Cote d'Ivoire). III. - Thomisidae. Bulletin de l Institut francais de Afrique Noire, 26, 1103 - 1143.","Ono, H. (1988) A revisional study of the spider family Thomisidae (Arachnida, Araneae) of Japan. National Science Museum, Tokyo, 252 pp.","Lessert, R. de (1919) Araignees du Kilimandjaro et du Merou (suite). III. Thomisidae. Revue suisse de zoologie, 27, 99 - 234."]}
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47. Mystaria budongo Honiball Lewis & Dippenaar-Schoeman 2014, sp. n
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Honiball Lewis, Allet S. and Dippenaar-Schoeman, Ansie S.
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Arthropoda ,Mystaria budongo ,Mystaria ,Arachnida ,Animalia ,Araneae ,Biodiversity ,Thomisidae ,Taxonomy - Abstract
Mystaria budongo sp. n. Figs 5, 10, 43, 44, 111–115 Type material: Holotype: ♂, RWANDA: Kibungo Province, Ibanda Makera, Rusumo [02°09’S, 30°55’E], alt. 1450 m, gallery forest canopy fogging of Teclea nobilis, October 1993, T. Wagner (ZFMK AR 1307). Paratypes: DEMOCRATIC REPUBLIC OF CONGO (DRC): Orientale Region, 1 ♂, Cyamudongo, Nyakabuye [02°34’S, 28°59’E], alt. 1750 m, canopy fogging Carapa grandiflora, October 1993, T. Wagner (ZFMK AR 1304). KENYA: Western Province, 2 ♂, Kakamega forest [00°22’N, 34°50’E], alt. 1600 m, secondary forest canopy fogging T. nobilis, January–February 2003, W. Freund (ZFMK AR 1305, 1306). RWANDA: Eastern Province, 3 ♂, Ibanda Makera, Rusumo [02°09’S, 30°55’E], alt. 1450 m, gallery forest canopy fogging T. nobilis, October 1993, T. Wagner (ZFMK AR 1308-1310). UGANDA: Masindi Province, 3 ♂, Budongo forest [01°45’N, 31°25’E], alt. 1200 m, secondary forest canopy fogging Cynometra alexandri, 15–25 January 1997, T. Wagner (ZFMK AR 1311, 1316, 1319); 2 ♂, Budongo forest [01°45’N, 31°25’E], alt 1200 m, primary forest canopy fogging C. alexandri, 15–25 January 1997, T. Wagner (ZFMK AR 1313, 1315); 1 ♂, same locality, swamp forest canopy fogging Rinorea beniensis, 15–25 January 1997, T. Wagner (ZFMK AR 1312); 3 ♂, Budongo forest [01°45’N, 31°25’E], alt. 1200 m, primary forest canopy fogging R. beniensis, 5–15 January 1997, T. Wagner (ZFMK AR 1314, 1317, 1318). Etymology. Named after the Budongo forest, where most specimens were sampled. Noun in apposition. Diagnosis. Differs from other species by pear-shaped carapace, narrowed in eye region, with pale orangeyellow median band centrally, dark brown-black bands laterally (Fig. 10), lateral eyes situated closest to median eyes with AME situated on slight tubercles and carapace. Legs pale yellow with distinct spiniform setae. Bulb with long and relatively strong embolus; RTA sturdy, long, finger-shaped, VTA almost of same length as RTA, tip with distinct curve (Figs 43, 44). Description. Female. Unknown. Male. Size, measurements (n = 2). TL: 2.80 (2.70–2.90); CL: 1.30 (1.22–1.37); CW: 1.23 (1.18–1.28); CI: 1.05 (1.03–1.07); CH: 0.65 (0.65–0.65); CLL: 0.19 (0.18–0.21); MOQ-L: 0.22 (0.22–0.22). Colour. Abdomen dark copper-brown laterally with orange-yellow band medially; ventrally pale. Carapace. Numerous long erectile setae present on postero-lateral edge of carapace and LE area. Chelicerae. As in (Fig 5). Sternum. SL: 0.70; SW: 0.64; SI: 1.10. Eyes. PME nearer to each other than to PLE, lateral eyes large; eye measurements: AME–AME: 0.21; ALE–AME: 0.24; AME–AME/AME–ALE: 0.88; PME–PME: 0.25; PLE–PME: 0.31; PME–PME/PME–PLE: 0.80; ALE/AME: 1.13; PLE/PME: 1.6; MOQ-AW/MOQ-PW: 0.85; MOQ-L/MOQ-W: 0.26; Clyp/AME–AME: 0.91. Legs. Long with long spiniform setae present on femora and patellae of legs I–IV and ventrally on tibiae and metatarsi; spiniform setae on tibiae and metatarsi I and II often twice as long as on other leg segments; claws and claw tufts as in Figs 111–114; leg formula: II:I:III:IV; leg measurements: leg I—Fe 1.14, Pat 0.34, Tib 1.08, Mt 0.81, Ta 0.61, total 3.99; II—Fe 1.42, Pat 0.41, Tib 1.35, Mt 1.09, Ta 0.31, total 4.58; III—Fe 0.81, Pat 0.28, Tib 0.70, Mt 0.50, Ta 0.34, total 2.64; IV—Fe 0.80, Pat 0.28, Tib 0.68, Mt 0.48, Ta 0.36, total 2.60. Abdomen. With scutum long-oval shaped; AL: 1.51; AW: 1.10; AI: 1.40. Palp. Embolus long, darkly sclerotized; wide space between VTA and RTA, RTA with black tip (Fig. 44). Female. Unknown. Natural history. Specimens were collected from primary and secondary forest canopy using fogging. They were sampled from various tree species such as Carapa grandiflora, Cynometra alexandri, Rinorea beniensis and Teclea nobilis. Only males are known and they were sampled between October and February. Distribution. Democratic Republic of Congo (DRC), Kenya, Rwanda and Uganda (Fig. 115)., Published as part of Honiball Lewis, Allet S. & Dippenaar-Schoeman, Ansie S., 2014, Revision of the spider genus Mystaria Simon, 1895 (Araneae: Thomisidae) and the description of a new genus from the Afrotropical region, pp. 101-144 in Zootaxa 3873 (2) on pages 114-118, DOI: 10.11646/zootaxa.3873.2.1, http://zenodo.org/record/4948115, {"references":["Simon, E. (1895) Histoire naturelle des Araignees. Vol. 1. Roret, Paris, 1084 pp. http: // dx. doi. org / 10.5962 / bhl. title. 51973","Lawrence, R. F. (1952) A collection of cavernicolous and termitophilous Arachnida from the Belgian Congo. Revue de zoologie et de botanique africaines, 46, 1 - 17.","Lawrence, R. F. (1927) Contributions to a knowledge of the fauna of South-West Africa V. Arachnida. Annals of the South African Museum, 25, 1 - 75."]}
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48. Mystaria decorata Honiball Lewis & Dippenaar-Schoeman 2014, comb. n
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Honiball Lewis, Allet S. and Dippenaar-Schoeman, Ansie S.
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Arthropoda ,Mystaria ,Arachnida ,Animalia ,Araneae ,Biodiversity ,Thomisidae ,Taxonomy ,Mystaria decorata - Abstract
Mystaria decorata (Lessert, 1919) comb. n. Paramystaria decorata Lessert 1919: 106, pl. 2, figs 25, 33 (descr. ♀). Remarks. The female holotype of this species is described from Tanzania: Kilimanjaro Region, Kibongoto, but the specimen could not be located. The species cannot be positively identified without the holotype. According to Lessert (1919), this species resembles Mystaria rufolimbata in the colour of the legs but differs from it in size and stronger abdominal spots., Published as part of Honiball Lewis, Allet S. & Dippenaar-Schoeman, Ansie S., 2014, Revision of the spider genus Mystaria Simon, 1895 (Araneae: Thomisidae) and the description of a new genus from the Afrotropical region, pp. 101-144 in Zootaxa 3873 (2) on page 135, DOI: 10.11646/zootaxa.3873.2.1, http://zenodo.org/record/4948115, {"references":["Lessert, R. de (1919) Araignees du Kilimandjaro et du Merou (suite). III. Thomisidae. Revue suisse de zoologie, 27, 99 - 234."]}
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49. Animalia
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Honiball Lewis, Allet S. and Dippenaar-Schoeman, Ansie S.
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Animalia ,Biodiversity ,Taxonomy - Abstract
Key to genera of the Mystarini -Apyretini -Tagulini tribes of the Afrotropical crab spiders 1. Median eyes unequal in size, PME very small............................................................... 2 - MOQ eyes fairly equal in size............................................................................4 2. Carapace wide with long erectile setae situated on small tubercles on posterior-thoracic edge; PME situated nearer to PLE than to each other............................................................... Apyretina Strand, 1929 (Apyretini) - Carapace convex to square or dorsally planar; long setae absent; posterior eyes almost equidistant from each other........ 3 3. MOQ area much wider than long, wider anteriorly than posteriorly................. Zametopias Thorell 1892 (Apyretini) - MOQ area slightly wider than long, anteriorly slightly narrower than posteriorly (Figs 139, 140)............ Leroya gen. n. 4. Carapace with leaf-shaped setae next to lateral eyes................................... Tagulis Simon, 1895 (Tagulini) - Carapace without leaf-shaped setae next to lateral eye area.................................................... 5 5. Carapace with numerous long erectile setae on posterior-thoracic edge, fovea and laterad to eye region, ant-like, chelicerae without cheliceral teeth, body and legs usually uniform brown........................ Sylligma Simon, 1895 (Mystarini) - Carapace only sometimes with a few long setae, not ant-like, but with large abdomens compared to carapace, chelicerae with three cheliceral teeth, body and legs usually with markings........................... Mystaria Simon, 1895 (Mystarini)
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50. Leroya unicolor Honiball Lewis & Dippenaar-Schoeman 2014, comb. n
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Honiball Lewis, Allet S. and Dippenaar-Schoeman, Ansie S.
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Arthropoda ,Leroya unicolor ,Arachnida ,Animalia ,Araneae ,Biodiversity ,Thomisidae ,Leroya ,Taxonomy - Abstract
Leroya unicolor (Simon, 1895) comb. n. Figs 137, 138, 140, 145, 146, 148 Mystaria unicolor Simon 1895: 989–990 (descr. ♀). Type material: Holotype: (designated by Simon 1895): ♀ specimen was collected from West Africa, Sierra Leone. Type series from MNHN was examined. Other material examined. DEMOCRATIC REPUBLIC OF CONGO (DRC): Orientale Region, 1 ♀, Rwankwi [01°20’S, 29°22’E], July 1951, J. Leroy (MRAC 71632). CÔTE D’ IVOIRE : Moyen-Comoé Region, 1 sub-adult ♂, Appouesso, F.C. Bossematie [6°37’N, 3°26’W], collected by hand in rainforest, 13 February 1997, R. Jocqué & L. Baert (MRAC 205.408). Diagnosis. Carapace orange to copper; abdomen pale brown (Fig. 137); carapace with few, short setae; body larger than L. silva. Female epigyne a solid circular sclerotised area, extending to a very short straight distance, centrally to posteriorly (Figs 138, 145). Re-description. Female. Size, measurements: (n = 2). TL: 4.77 (3.46–5.21); CL: 1.81 (1.49–1.92); CW: 1.77 (1.38–1.91); CI: 1.03 (1.01–1.08); CH: 0.94 (0.71–1.02); CLL: 0.19 (0.10–0.22); MOQ-L: 0.32 (0.26–0.34). Colour. carapace metallic shine, orange to copper; abdomen pale brown. Carapace. slightly longer than wide (Fig. 137). Sternum. SL: 0.72; SW: 0.77; SI: 0.93. Clypeus. as in Fig. 140. Eye s. not situated on tubercles, no eye spots; eye measurements: AME–AME: 0.56; ALE-AME: 0.54; AME-AME/AME-ALE: 1.03; PME-PME: 0.68; PLE-PME: 0.61; PME-PME/PME-PLE: 1.11; ALE/AME: 0.97; PLE/PME: 0.91; MOQ-AW/MOQ-PW: 0.83; MOQ-L/ MOQ-W: 0.39; Clyp/AME-AME: 0.32. Legs. dense setae on all leg segments; trichobothria not very conspicuous probably present on all legs, seen on metatarsi and tarsi II-III; leg formula: II:I:III:IV; leg measurements: leg I—Fe 1.23, Pat 0.47, Tib 1.20, Mt 1.02, Ta 0.76, total 4.57; II—Fe 1.31, Pat 0.46, Tib 1.22, Mt 1.03, Ta 0.72, total 4.73; III—Fe 1.11, Pat 0.27, Tib 0.73, Mt 0.54, Ta 0.45, total 3.10; IV—Fe 1.03, Pat 0.28, Tib 0.66, Mt 0.54, Ta 0.44, total 2.95. Abdomen. large in comparison to carapace; covered with fine setae, small sigillae; AL: 2.96; AW: 2.97; AI: 1.00. Epigyne. intromittent canals and spermathecae as in Fig. 146. Male. Unknown. Natural history. This species was collected in rainforests. Adult females were sampled during July and a subadult male during February. Distribution. Sierra Leone. New records: Democratic Republic of Congo (DRC) and Côte d’Ivoire (Fig. 148)., Published as part of Honiball Lewis, Allet S. & Dippenaar-Schoeman, Ansie S., 2014, Revision of the spider genus Mystaria Simon, 1895 (Araneae: Thomisidae) and the description of a new genus from the Afrotropical region, pp. 101-144 in Zootaxa 3873 (2) on pages 139-140, DOI: 10.11646/zootaxa.3873.2.1, http://zenodo.org/record/4948115, {"references":["Simon, E. (1895) Histoire naturelle des Araignees. Vol. 1. Roret, Paris, 1084 pp. http: // dx. doi. org / 10.5962 / bhl. title. 51973"]}
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