272 results on '"chernetidae"'
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2. First record of phoresy on the genus Oreodera Audinet-Serville, 1835 (Coleoptera: Cerambycidae) by the pseudoscorpion Cordylochernes scorpioides (Linnaeus, 1758) (Arachnida: Pseudoscorpiones)
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Juan P. Botero, Alejandro Lopera-Toro, Sergio Mendez-Cardona, and Adrián Forsyth
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chernetidae ,dispersion method ,long-hotn beetles ,peru ,Science ,Zoology ,QL1-991 - Abstract
The phoretic association of the pseudoscorpion Cordylochernes scorpioides (Linnaeus, 1758) (Chernetidae) on the long-horn beetle Oreodera rufofasciata Bates, 1861 (Coleoptera: Cerambycidae) is reported for the first time.
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- 2023
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3. A new species of Epichernes (Pseudoscorpiones: Chernetidae) associated with rodents in Costa Rica.
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Villegas-Guzmán, Gabriel A., Chinchilla-Romero, Federico A., and Martínez, Ramy Jhasser
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PSEUDOSCORPIONS , *RODENTS , *SPECIES , *SETAE , *FEMUR , *MURIDAE - Abstract
The genus Epichernes Muchmore, 1982 has three Neotropical species with specific rodent hosts. Epichernes vickeryae sp. nov. is here described from Monteverde, Puntarenas, Costa Rica: the specimens were collected from a spiny pocket mouse Heteromys nubicolens. The new species, named E. vickeryae, is closer to E. navarroi by the position of trichobothria setae ist and isb, which are adjacent and the number of teeth on the movable finger, known from Mexico. The new species is characterized by trichobothrium ist adjacent to isb, femur L/B 1.71–1.85, it has 22–31 external accessory teeth, 58 teeth on fixed finger and 62 on movable finger. The carapace ranging from 1.12 mm to 1.33 mm in length, central tergites with 21–22 setae, chelicera with five setae on the hand, sb and b denticulate. The new species represents the second known species of Epichernes from Costa Rica. [ABSTRACT FROM AUTHOR]
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- 2023
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4. Phoretic behavior of the pseudoscorpion Megachernes ryugadensis on the Japanese wood mouse Apodemus speciosus.
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Shimada, Takuya, Okabe, Kimiko, Makino, Shun'ichi, Nakamura, Shoko, and Fujii, Saori
- Abstract
Phoresy is a passive transportation behavior where one organism (phoront) disperses to a new location by attaching to another organism. Pseudoscorpions are arthropod predators that mainly live in soil, subterranean habitats, and under tree bark. Some species also live in animal nests and engage in phoresy on small mammals, suggesting close associations with these animals. However, the relationship between phoretic pseudoscorpions and hosts as well as the ecological significance of phoresy remain largely unexplored. Here, to understand the function of phoresy of Megachernes ryugadensis, phoretic on small mammals, their phoretic behavior was investigated in a deciduous forest in northern Japan; individual-level dynamics of phoresy were examined by over 3-year mark-recapture surveys that concurrently marked the host and phoront; and host characteristics, such as sex and age class, were analyzed based on a 2-year small mammal trapping survey. The primary host species was the abundant Japanese wood mouse Apodemus speciosus. Out of 132 pseudoscorpions marked, 5 were recaptured approximately 1 month later. No pseudoscorpions were recaptured within the same census period (3–4 days) when they were marked, indicating that phoresy events last less than one night, and pseudoscorpions are unlikely to engage in phoresy again within a few weeks of their initial engagement. Furthermore, analysis of host characteristics revealed a tendency for female mice and adult individuals to have a higher probability of being hosts compared with males and subadults, respectively. Based on the findings in this and previous studies, the function of phoresy in this species is discussed. [ABSTRACT FROM AUTHOR]
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- 2023
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5. The first record of Pselaphochernes scorpioides (Hermann, 1804) from Georgia, Caucasus (Arachnida: Pseudoscorpiones).
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Gogshelidze, Mariam and Novák, János
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PSEUDOSCORPIONS , *ARACHNIDA , *NATIONAL parks & reserves - Abstract
Pselaphochernes scorpioides (Hermann, 1804) is reported from Georgia for the first time. This is also the first record of the genus Pselaphochernes in Georgia. The finding is based on one female specimen found in the Malaise trap in Kintrishi National Park, Adjara Region. A description of the main morphological and morphometrical characteristics of the collected specimen is provided. [ABSTRACT FROM AUTHOR]
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- 2023
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6. Associated pseudoscorpions (Arachnida: Pseudoscorpiones) with waste heaps of Atta colombica (Guérin-Méneville, 1844) (Hymenoptera: Formicidae) in Panama
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Ramy Jhasser Martínez, Gabriel A. Villegas Guzmán, Dora Isabel Quirós, and Daniel Emmen
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ant nests ,atemnidae ,cheiridiidae ,chernetidae ,symbiosis ,Science ,Zoology ,QL1-991 - Abstract
Waste heaps of Atta are host to an extraordinary diversity of myrmecophiles insects and other arthropods. In this study, the presence of four species of pseudoscorpions is recorded in two Atta colombica waste heaps in the years 2016 and 2017. Two of these species, Cordylochernes scorpioides and Lustrochernes carolinensis are new records in waste heaps and except for the deutonymphs of L. carolinensis, the others all stages of post-embryonic development were present in the studied heaps, which could indicate that these two species carry out their entire life cycle in these waste mounds and live there permanently.
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- 2021
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7. NEW RECORDS OF CHERNETID AND CHELIFERID SPECIES (ARACHNIDA: PSEUDOSCORPIONES) FROM NORTH MACEDONIA.
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ČERVENÁ, MARTINA, SELNEKOVIČ, DÁVID, and CHRISTOPHORYOVÁ, JANA
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ARACHNIDA ,PSEUDOSCORPIONS ,SPECIES - Abstract
Copyright of Natura Croatica is the property of Natura Croatica and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)
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- 2021
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- View/download PDF
8. New pseudoscorpions of the genera 'Americhernes' Muchmore and 'Cordylochernes' Beier from Australia (Pseudoscorpionida: Chernetidae)
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Harvey, Mark S
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- 1990
9. Parachernes (Parachernes) nitidimanus
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Bedoya-Roqueme, Edwin, Tizo-Pedroso, Everton, Barbier, Eder, and Lira, André Felipe De Araújo
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Parachernes nitidimanus ,Parachernes ,Arthropoda ,Pseudoscorpiones ,Arachnida ,Chernetidae ,Animalia ,Biodiversity ,Taxonomy - Abstract
Parachernes (Parachernes) nitidimanus (Ellingsen, 1905) Material examined. 1 female, Pernambuco, Brazil: Furna do Morcego cave, 8°34’14.1”S; 37°22’55.6”W, 556 m a.s.l., 09-V-2019; Catimbau National Park, E. Barbier leg. (LECA; Ps-SCR010). Diagnosis. According to Ellingsen (1905) and Beier (1932b) can be easily distinguished from the other species of the genus Parachernes Chamberlin (1931) by the carapace as long as broad 1.14×, gradually narrowing forwards, the short frontal margin straightened. Metazone distinctly granulated, yet a little glossy before the first furrow. Two distinct transverse furrows, the anterior one about in the middle, the posterior one somewhat nearer to the hinder margin than to the anterior furrow. Tergite divided (except XI), slightly granulated, al setae rather long, slightly clavate. Chaetotaxy tergal: 10: 10: 10: 8(1): 8(2): 6(2): 8(2): 8(2): 8(2): 10(2): 4(2ST):2. Genital region opercula with a central group of 18 short, three setae on each side, and ten marginal setae. Chelicerae, female with galea very slender and short, with some fine teeth in and near the extremity on the underside, male with about 6 terminal branches; paired spermatheca, typical of the genus. Pedipalps moderately strong, all segments smooth and glossy. The setae on the inner side of the trochanter and femur are slightly clavate, the other setae of the palps are slightly dentate in the extremity, on the fingers simple with some longer ones intermixed; trochanter and the proximal part of femur slightly shagreened; femur 2.35×, strongly granulated; patella 2.02×, more slightly, rather shagreened. chela with pedicel 3.18×, chela without pedicel 2.47×, hand round about smooth and very glossy, fingers as general smooth and glossy. Measurements (mm). Body length: 2.359. Carapace: 0.771 / 0.672. Pedipalps: trochanter: 0.347 / 0.197, femur: 0.544 / 0.235, patella: 0.589 / 0.266, chela with pedicel: 1.064 / 0.384, chela without pedicel: 0.950 / 0.384, movable finger: 0.538. Chelicera: 0.277 / 0.141, movable finger length:0.202. Leg I: femur: 0.105 / 0.127, patella: 0.317 / 0.137, tibia: 0.272 / 0.091, tarsus: 0.308 / 0.071. Leg IV: femur+patella: 0.569 / 0.158, tibia: 0.318 / 0.103, tarsus: 0.255 / 0.052. Distribution. Brazil, Saint Vincent, and the Grenadines (Harvey 2013; World Pseudoscorpiones Catalog 2022)., Published as part of Bedoya-Roqueme, Edwin, Tizo-Pedroso, Everton, Barbier, Eder & Lira, André Felipe De Araújo, 2023, Two new cave-dwelling pseudoscorpion species (Arachnida: Pseudoscorpiones) from Northeastern Brazil, pp. 317-332 in Zootaxa 5293 (2) on page 320, DOI: 10.11646/zootaxa.5293.2.6, http://zenodo.org/record/7960232, {"references":["Ellingsen, E. (1905) Pseudoscorpions from South America collected by Dr. A. Borelli, A. Bertoni de Winkelried, and Prof. Goeldi. Bollettino dei Musei di Zoologia e di Anatomia Comparata della R. Universita di Torino, 20 (500), 1 - 17. https: // doi. org / 10.5962 / bhl. part. 9304","Beier, M. (1932 b) Pseudoscorpionidea II. Subord. C. Cheliferinea. Tierreich, 58, i - xxi + 1 - 294.","Chamberlin, J. C. (1931) The arachnid order Chelonethida. Stanford University Publications, Biological Science, 7 (1), 1 - 284.","Harvey, M. S. (2013) Pseudoscorpions of the World. Version 3.0. Western Australian Museum, Perth. Available from: http: // www. museum. wa. gov. au / catalogues / pseudoscorpions (accessed 20 February 2023)","World Pseudoscorpiones Catalog (2022) World Pseudoscorpiones Catalog. Natural History Museum Bern. Available from: http: // wac. nmbe. ch (accessed 20 February 2022)"]}
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- 2023
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10. Ceriochernes foliaceosetosus Beier 1974
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Bedoya-Roqueme, Edwin, Tizo-Pedroso, Everton, Barbier, Eder, and Lira, André Felipe De Araújo
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Arthropoda ,Pseudoscorpiones ,Ceriochernes ,Arachnida ,Chernetidae ,Animalia ,Biodiversity ,Ceriochernes foliaceosetosus ,Taxonomy - Abstract
Ceriochernes foliaceosetosus Beier, 1974 Material examined. 1 female, Pernambuco, Brazil: Meu Rei cave, 08°29’14.1”S, 37° 16’48.8”W, 777 m a.s.l., 19- I-2016, Catimbau National Park, E. Barbier leg. (LECA; Ps-012). Diagnosis. According to the description made by Beier (1974), the specimens of Ceriochernes foliaceosetosus Beier, 1974 can be easily distinguished by the carapace reddish-brown, slightly longer than wide, without eyes and eyespots, strongly granulated, the granules of the metazone covered with an epicuticle, reticulate in the form of a rough honeycomb, both transverse furrow narrow and not very deep, but distinct, the anterior curved laterally, the posterior closer to the rear margin, with six setae on the anterior margin, and eight on the posterior margin. All tergites divided, setae clavate and broadly foliated, rounded at the tip, curved and almost sessile, partially covered by epicuticle, with midrib, pleural membrane very densely granulated. Chaetotaxy tergal: 6: 8: 8: 6: 6: 8: 8: 8: 8: 8: 8: 2. Genital region operculum with a set of 12 setae, and ten setae on posterior margin. Chelicerae with six to seven setae on hand, es very short, three blades on the rallum, Serrula with 17 blades, galea with 5 very short branches distally. Pedipalps strongly reticulated, trochanter 1.0×, femur 2.58×, patella 2.15×, fingers not as long as the hand without pedicel, each with about 35–40 marginal teeth, the accessory teeth small and inconspicuous, present on the medial side only on the distal part of the finger, trichobothrium ist midway between isb and it, est proximal of ist; trichobothrium st closest to t. Measurements (mm). Body length: 2.021. Carapace: 0.638 / 0.538. Pedipalps: trochanter: 0.344 / 0.244, femur: 0.522 / 0.204, patella: 0.569 / 0.204, chela with pedicel: 0.864 / 0.346, chela without pedicel: 0.833 / 0.346, movable finger: 0.383. Leg I: trochanter: 0.124 / 0.105, femur: 0.127 / 0.093, patella: 0.255 / 0.093, tibia: 0.275 / 0.072, tarsus: 0.283 / 0.053. Leg IV: trochanter: 0.183 / 0.140, femur+patella: 0.488 / 0.152, tibia: 0.377 / 0.109, tarsus: 0.385 / 0.088. Distribution. Brazil (Harvey 2013; World Pseudoscorpiones Catalog 2022)., Published as part of Bedoya-Roqueme, Edwin, Tizo-Pedroso, Everton, Barbier, Eder & Lira, André Felipe De Araújo, 2023, Two new cave-dwelling pseudoscorpion species (Arachnida: Pseudoscorpiones) from Northeastern Brazil, pp. 317-332 in Zootaxa 5293 (2) on page 321, DOI: 10.11646/zootaxa.5293.2.6, http://zenodo.org/record/7960232, {"references":["Beier, M. (1974) Brasilianische Pseudoscorpione aus dem Museum in Genf. Revue Suisse de Zoologie, 81, 899 - 909. https: // doi. org / 10.5962 / bhl. part. 76050","Harvey, M. S. (2013) Pseudoscorpions of the World. Version 3.0. Western Australian Museum, Perth. Available from: http: // www. museum. wa. gov. au / catalogues / pseudoscorpions (accessed 20 February 2023)","World Pseudoscorpiones Catalog (2022) World Pseudoscorpiones Catalog. Natural History Museum Bern. Available from: http: // wac. nmbe. ch (accessed 20 February 2022)"]}
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- 2023
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11. Petterchernes brasiliensis Heurtault 1986
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Bedoya-Roqueme, Edwin, Tizo-Pedroso, Everton, Barbier, Eder, and Lira, André Felipe De Araújo
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Petterchernes brasiliensis ,Arthropoda ,Pseudoscorpiones ,Petterchernes ,Arachnida ,Chernetidae ,Animalia ,Biodiversity ,Taxonomy - Abstract
Petterchernes brasiliensis Heurtault, 1986 Material examined. 1 male, Pernambuco, Brazil: Furna do Morcego cave, 8°34’14.1”S; 37°22’55.6”W, 556 m a.s.l., 09-V-2019; Catimbau National Park, E. Barbier leg. (LECA; Ps-SCR011). Diagnosis. According to Heurtault (1986) and Mahnert (1994) the males of Petterchernes brasiliensis Heurtault, 1986 can be easily distinguished by the carapace without eyes and without eyespots, dark brown, metazone finely granulated, setae of the carapace and tergites strongly clavate, with two deep transverse furrows, for setae on anterior margin; tergites divided, granulate. Chaetotaxy tergal: 9: 9: 9: 10: 10: 10: 12: 12: 10: 10: 10: 2. Genital region operculum with 32 setae and ten setae on posterior margin. Chelicerae, galea with multiple branches, and three blades in the rallum. Pedipalps coarsely granulate, setae stout and enlarged, trochanter 1.67×, with high dorsal hump, femur 2.22×, abruptly enlarged, patella 2.15×, chela with pedicel 2.28×, chela without pedicel 2.09×, trichobothrium isb, ib, and est at same level, hand with well pronounced internal hump bearing some longer and stouter setae. Legs, tarsus IV without tactile setae, claws smooth and simple, subterminal seta smooth, curve. Measurements (mm). Body length: 1.251. Carapace: 0.554 / 0.473. Pedipalps: trochanter: 0.269 / 0.161, femur: 0.477 / 0.214, patella: 0.415 / 0.193, chela with pedicel: 0.766 / 0.335, chela without pedicel: 0.7020 / 0.335, movable finger: 0.418. Leg I: trochanter: 0.137 / 0.085, femur: 0.131 / 0.115, patella: 0.106 / 0.076, tibia: 0.127 / 0.078, tarsus: 0.202 / 0.047. Leg IV: trochanter: 0.153 / 0.121, femur+patella: 0.380 / 0.121, tibia: 0.164 / 0.086, tarsus: 0.276 / 0.058. Distribution. Brazil (Harvey 2013; World Pseudoscorpiones Catalog 2022)., Published as part of Bedoya-Roqueme, Edwin, Tizo-Pedroso, Everton, Barbier, Eder & Lira, André Felipe De Araújo, 2023, Two new cave-dwelling pseudoscorpion species (Arachnida: Pseudoscorpiones) from Northeastern Brazil, pp. 317-332 in Zootaxa 5293 (2) on page 321, DOI: 10.11646/zootaxa.5293.2.6, http://zenodo.org/record/7960232, {"references":["Heurtault, J. (1986) Petterchernes brasiliensis, genre et espece nouveaux de Pseudoscorpions du Bresil (Arachnides, Pseudoscorpionida, Chernetidae). Bulletin du Museum National d'Histoire Naturelle, Paris, 8, 351 - 355.","Mahnert, V. (1994) New chernetid pseuuoscorpions (Pseudoscorpionida: Chemetidae) from Venezuela and Brazil, with remarks on the genus Ancalochernes Beier. Revue suisse de Zoologie, 101, 829 - 838. https: // doi. org / 10.5962 / bhl. part. 79929","Harvey, M. S. (2013) Pseudoscorpions of the World. Version 3.0. Western Australian Museum, Perth. Available from: http: // www. museum. wa. gov. au / catalogues / pseudoscorpions (accessed 20 February 2023)","World Pseudoscorpiones Catalog (2022) World Pseudoscorpiones Catalog. Natural History Museum Bern. Available from: http: // wac. nmbe. ch (accessed 20 February 2022)"]}
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- 2023
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12. Two new cave-dwelling pseudoscorpion species (Arachnida: Pseudoscorpiones) from Northeastern Brazil
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EDWIN BEDOYA-ROQUEME, EVERTON TIZO-PEDROSO, EDER BARBIER, and ANDRÉ FELIPE DE ARAÚJO LIRA
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Chthoniidae ,Arthropoda ,Pseudoscorpiones ,Arachnida ,Chernetidae ,Geogarypidae ,Animalia ,Animal Science and Zoology ,Biodiversity ,Hesperolpiidae ,Ecology, Evolution, Behavior and Systematics ,Taxonomy - Abstract
In a study of pseudoscorpions in caves from the northeastern Brazil, eight species of Pseudoscorpiones were identified. The known distribution of the species Pseudochthonius biseriatus Mahnert, 2001, Cryptoditha aff. elegans, Parachernes (P.) nitidimanus (Ellingsen, 1905), Petterchernes brasiliensis Heurtault, 1986, Ceriochernes foliaceosetosus Beier, 1974, and Progarypus setifer Mahnert, 2001 is extended to include the State of Pernambuco. Additionally, Geogarypus gollumi sp. nov. (Geogarypidae) and Progarypus smaugi sp. nov. (Hesperolpiidae) are described as new species.
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- 2023
13. Phoretic behavior of the pseudoscorpion Megachernes ryugadensis on the Japanese wood mouse Apodemus speciosus.
- Author
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Shimada T, Okabe K, Makino S, Nakamura S, and Fujii S
- Subjects
- Animals, Male, Mice, Forests, Japan, Female, Arthropods, Murinae, Behavior, Animal, Animal Distribution
- Abstract
Phoresy is a passive transportation behavior where one organism (phoront) disperses to a new location by attaching to another organism. Pseudoscorpions are arthropod predators that mainly live in soil, subterranean habitats, and under tree bark. Some species also live in animal nests and engage in phoresy on small mammals, suggesting close associations with these animals. However, the relationship between phoretic pseudoscorpions and hosts as well as the ecological significance of phoresy remain largely unexplored. Here, to understand the function of phoresy of Megachernes ryugadensis, phoretic on small mammals, their phoretic behavior was investigated in a deciduous forest in northern Japan; individual-level dynamics of phoresy were examined by over 3-year mark-recapture surveys that concurrently marked the host and phoront; and host characteristics, such as sex and age class, were analyzed based on a 2-year small mammal trapping survey. The primary host species was the abundant Japanese wood mouse Apodemus speciosus. Out of 132 pseudoscorpions marked, 5 were recaptured approximately 1 month later. No pseudoscorpions were recaptured within the same census period (3-4 days) when they were marked, indicating that phoresy events last less than one night, and pseudoscorpions are unlikely to engage in phoresy again within a few weeks of their initial engagement. Furthermore, analysis of host characteristics revealed a tendency for female mice and adult individuals to have a higher probability of being hosts compared with males and subadults, respectively. Based on the findings in this and previous studies, the function of phoresy in this species is discussed., (© 2023. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.)
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- 2023
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14. Two new species of pseudoscorpions (Arachnida: Pseudoscorpiones) from a Mexican oak forest near Pico de Orizaba National Park.
- Author
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Piedra-Jiménez, Dulce F., Alvarez-Padilla, Fernando, and González-Santillán, Edmundo
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PSEUDOSCORPIONS , *NATIONAL parks & reserves , *ARACHNIDA , *FOREST litter , *SPECIES , *BEETLES - Abstract
A faunistic inventory from an oak forest near Pico de Orizaba National Park revealed the presence of two new species of pseudoscorpions. Atherochernes breviductus sp. nov. of the family Chernetidae is represented by 286 mature specimens, and is the first record of this genus for the country; Serianus orizabensis sp. nov. of the family Garypinidae is represented by 44 adults and is the first record of the family for the State of Veracruz. Most individuals were collected by sifting leaf litter and processing with Berlese funnels. The new taxa are hereby described and documented with illustrations and high-quality microphotography. The relationships of AtherochernesBeier, 1954 with other chernetids was investigated with a molecular phylogeny. In addition, the species Mexichelifer reddelliMuchmore, 1973 and Mundochthonius mexicanusMuchmore, 1973 are recorded for the first time in the state of Veracruz. [ABSTRACT FROM AUTHOR]
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- 2019
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15. The Status of the Central American Pseudoscorpion Genus Coprochernes Beier, 1976, a New Synonym of Neoallochernes Hoff, 1947 (Pseudoscorpiones: Chernetidae).
- Author
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Harvey, Mark S. and Mahnert, Volker
- Subjects
- *
CHERNETIDAE , *PSEUDOSCORPIONS , *MORPHOLOGY , *SPECIES , *TAXONOMY - Abstract
The pseudoscorpion genus CoprochernesBeier, 1976 currently includes two species from Central America. The type species, C. costaricensisBeier, 1976, was collected from mammal dung in Costa Rica. A restudy of the type specimens reveals that it has all of the salient morphological features of the genus NeoallochernesHoff, 1947, including only four setae on the cheliceral hand and a pair of conical spermathecae with darkened tips. Thus, Coprochernes costaricensis is transferred to Neoallochernes, forming the new combination Neoallochernes costaricensis (Beier, 1976), and rendering CoprochernesBeier, 1976 as a new junior synonym of Neoallochernes. The only other species of Coprochernes, C. quintanarooensisMuchmore, 1991 from Mexico, is also transferred to Neoallochernes, forming the new combination N. quintanarooensis (Muchmore, 1991); but, because it lacks the diagnostic features of Neoallochernes, its generic position is provisional. New illustrations are provided for N. stercoreus (Turk, 1949) based on specimens from the type locality in central Texas. [ABSTRACT FROM AUTHOR]
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- 2019
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16. A new cave-dwelling Maxchernes Feio, 1960 (Pseudoscorpiones: Chernetidae) from Brazil
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Everton Tizo-Pedroso, André Felipe de Araujo Lira, Eder Barbier, and Edwin Bedoya-Roqueme
- Subjects
geography ,geography.geographical_feature_category ,biology ,Ecology ,Chernetidae ,Speleology ,biology.organism_classification ,Tropical forest ,Cave dwelling ,Cave ,Genus ,Animal Science and Zoology ,Taxonomy (biology) ,Ecology, Evolution, Behavior and Systematics - Abstract
During a survey of caves in a seasonally dry tropical forest area in northeastern Brazil, a new species of the genus Maxchernes was discovered and it is formally described here. The new species, na...
- Published
- 2021
17. CONFIRMED RECORD OF THE GENUS CHERNES IN BOSNIA AND HERZEGOVINA (PSEUDOSCORPIONES: CHERNETIDAE).
- Author
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CHRISTOPHORYOVÁ, JANA, ČERVENÁ, MARTINA, and KRAJČOVIČOVÁ, KATARÍNA
- Subjects
PSEUDOSCORPIONS ,CHERNETIDAE ,PLANT species ,HABITATS ,BOTANICAL specimens ,SPECIES distribution - Abstract
Copyright of Natura Croatica is the property of Natura Croatica and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)
- Published
- 2018
- Full Text
- View/download PDF
18. Rhopalochernes luiscarlosi Marimon & Blanco & Harvey 2022, sp. nov
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Marimon, Karla, Blanco, Eduardo Villarreal, and Harvey, Rk. S.
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Rhopalochernes ,Arthropoda ,Pseudoscorpiones ,Rhopalochernes luiscarlosi ,Arachnida ,Chernetidae ,Animalia ,Biodiversity ,Taxonomy - Abstract
Rhopalochernes luiscarlosi sp. nov. Figs. 1A–F, 2A–G, 3A–G, 7A ZooBank Registration: urn:lsid:zoobank.org:pub: 82D786A8-5B1A-4CF5-8194-64EF3B303633 Type material. female holotype: COLOMBIA, Bolívar, Municipio de San Jacinto, Vereda La Flecha, Finca Amanecer Gaitero (9°51′09.74″N; 75°10′32.32″W), 250 masl. 10.XI.2019, K. Marimon & E. Villarreal leg. (ICN.APs841). Paratypes: 1 male and 2 females, with same data as for holotype. (IAvH-I-3866 [1♀]; (IAvH-I-3876 [1♀]; ICN-APs-842 [1♂]), Etymology. The specific epithet is a patronym in honor of the late professor Luis Carlos Gutierrez Moreno, who was a lead researcher in the Caribbean region of Colombia, as well as founder of the research group Biodiversidad del Caribe Colombiano at Universidad del Atlántico. Diagnosis. Rhopalochernes luiscarlosi sp. nov. is characterized by the following combination of characters: cheliceral hand with four setae (Figs. 2F, 3F); serrula exterior with 11 blades; eyeless (Figs. 1A, 1C, 1D, 1F); carapace with two deep transverse furrows (Figs. 1C, 1F); nodus ramosus proximal to st (Figs. 2E, 3E); and trichobothria st closer to t than sb (Figs. 2E, 3E). Differential diagnosis: Rhopalochernes luiscarlosi sp. nov. can be differentiated from R. chamberlini, R. panamensis and R. ohausi by the lack of eyespots. It also differs from R. chamberlini by the position of the nodus ramosus which is midway between sb and st (Figs. 2E, 3E), but at the same level as st in R. chamberlini. It can be separated from R. panamensis by the serrula exterior which has 11‒12 blades in R. luiscarlosi sp. nov. and 14‒15 blades in R. panamensis. From the type species, R. ohausi, R. luiscarlosi sp. nov. is distinguished by having gaping chelal fingers (not gaping chelal fingers in R. ohausi) and the position of nodus ramosus which is proximal to or at same level of st in R. ohausi (see Mahnert, 2001 Fig. 110). Rhopalochernes luiscarlosi sp. nov. is similar to R. insulanus and R. catalinae sp. nov. by the absence of eyes, but can be differentiated from R. insulanus by the presence of 4 setae on the cheliceral hand (6 in R. insulanus), a trait that is also present in R. chamberlini, R. panamensis and R. catalinae sp. nov. (see Heurtault, 1998, Figs. 4, 9). It can be distinguished from R. catalinae sp. nov. by the furrows on the surface of the carapace, which are deep and conspicuous in R. luiscarlosi sp. nov. (Figs. 1C, 1F), but shallow and inconspicuous in R. catalinae sp. nov. (Figs. 4C, 4F). Additionally, they differ by the shape of the spermathecae, which have elongated and narrow ducts in R. luiscarlosi sp. nov. (Fig. 7A) but have short, thick ducts in R. catalinae sp. nov. (Fig. 7B). Finally, R. luiscarlosi sp. nov. has a slender tarsus IV (4.00–4.25 × longer than deep) while that of R. catalinae sp. nov. is more robust (2.75–3.75 × longer than deep). Description of adult: Colour: Carapace and pedipalps reddish brown. Tergites and legs yellowish brown (Fig. 1A–F). Carapace: heavily granulated; 1.15‒1.23 (♂), 1.09‒1.27 (♀) × longer than broad, eyes or eye-spots absent; with 2 deep transverse furrows, posterior furrow closer to posterior margin than anterior furrow; posterior margin of carapace straight; anterior margin with 4 setae (♂, ♀), posterior margin with 8 (♂), 10 (♀) setae (Fig. 3C, F). Chelicera: 1.67‒1.80 (♂), 1.29‒1.83 (♀) × longer than broad; with 4 setae on hand (sbs absent) and 1 distal seta (gs) on movable finger, is, bs and es short and acuminate, ls longer and thicker (Figs. 2F, 3F); galea with 4 rami (♀) or simple (♂) (Figs. 2D, 3G); rallum with 3 blades (Figs. 2G, 3D), anterior blade with several ramifications while others smooth; serrula exterior with 11‒12 blades; lamina exterior present. Pedipalp: trochanter, femur, patella and chelal hand heavily granulated, with short, feathered and acuminate setae (Figs. 2C, 3C); chelal fingers smooth; trochanter 1.50‒1.62 (♂), 1.40‒1.71 (♀), femur 2.13‒2.19 (♂), 2.31‒2.67 (♀), patella 2.00‒2.20 (♂), 1.88‒2.20 (♀), chela (with pedicel) 2.60‒2.74 (♂), 2.80‒3.95 (♀), chela (without pedicel) 2.40‒2.53 (♂), 2.45‒2.63 (♀), hand 1.10‒1.21 (♂), 1.20‒1.26 (♀) × longer than broad, movable finger 1.09‒ 1.18 (♂), 1.04‒1.27 (♀) × longer than hand. All marginal teeth rounded except the terminal ones, which are pointed, accessory teeth not visible. Fixed chelal finger with 8 trichobothria, movable chelal finger with 4 trichobothria: eb and esb placed basally, est medially at equal distance from et and eb, and et distally near the tip of the fixed finger; ib at the same level as esb and close to ist, which is placed midway in the first half of the fixed finger, isb slightly more distal than est and it closer to et than isb; b, sb, st and t about an equal distance from each other, sb slightly ahead of esb, st in the middle of movable finger slightly closer to t than sb, t placed distally and closer to st than tip of the finger. Venom apparatus present only in movable chelal finger with nodus ramosus proximal to st (Figs. 2E, 3E). Coxal region: maxilla smooth except for the antero-lateral region; coxae smooth; manducatory process triangular in shape with 2 apical setae, 1 prolateral suboral seta and 12 (♂), 9 (♀) additional setae on maxilla. Median maxillary lyrifissure rounded and situated submedially. Chaetotaxy of coxae I‒IV, ♂, 9: 9: 8: 15; ♀, 10: 13: 11: 20. Legs: granulate; feathered setae on retrolateral margin and dentate setae on prolateral margins. Femur + patella of leg IV 2.45 ‒ 2.60 (♂), 2.73‒2.80 (♀) × longer than deep; tibia 3.14‒3.50 (♂), 3.14‒3.83 (♀) × longer than deep; tarsus 4.00‒4.25 (♂), 4.00‒4.50 (♀) × longer than deep. Tarsi III and IV with short tactile seta, located subdistally. Arolium undivided, slightly shorter than claws; claws slender and simple, not modified (Figs. 2A‒B, 3A‒B). Abdomen: tergites I‒X and sternites IV ‒X with a clear medial suture line (Figs. 7C). Tergal chaetotaxy: ♂, 10: 12: 12: 14: 14: 14: 15: 14: 14: 12: 9 (2 T): 2; ♀, 14: 12: 11: 15: 17: 16: 15: 14: 12: 13: 10 (2 T): 2; Sternal chaetotaxy: ♂, 17:(1) 8 (1): (1) 10 (1): 13: 14: 14: 12: 11: 9: 9: 2; ♀, 16: (1) 10 (1): (1) 9 (1): 14: 14: 15: 12: 10: 9: 4: 2. Genitalia: female: spermathecae paired, with long ducts ending in oval sacs (Fig. 7A). Male: genital opercula containing 9 setae on anterior operculum (sternite II), 8 setae clustered together just anterior to the aperture, 4 in posterior margin of aperture, and 4 in distal margin of posterior operculum (sternite III). Dimensions: holotype female (ICN APs-841), with range of 4 female paratype in parentheses: Body length 1.36 (1.12‒1.36). Pedipalps: trochanter 0.22/0.15 (0.21‒0.24/0.14‒0.15), femur 0.35/0.15 (0.33‒0.38/0.14‒0.16), patella 0.31/0.15 (0.31‒0.34/0.15‒0.17), chela (with pedicel) 0.56/0.2 (0.53‒0.56/0.18‒0.20), chela (without pedicel) 0.49 (0.49‒0.50), hand (without pedicel) length 0.24 (0.22‒0.24), movable finger length 0.27 (0.26‒0.28). Carapace 0.5/0.46 (0.49‒0.52/0.41‒0.46). Leg IV: femur + patella 0.28/0.10 (0.28‒0.30/0.22‒0.23), tibia 0.22/0.07 (0.22‒0.23/0.06‒0.07), tarsus 0.17/0.04 (0.16‒0.18/0.04). Allotype male (ICN APs-842), with other male in parentheses: Body length 1.18 (1.03). Pedipalps: trochanter 0.21/0.13 (0.21/0.14), femur 0.34/0.16 (0.35/0.16), patella 0.32/0.16 (0.33/0.15), chela (with pedicel) 0.52/0.19 (0.52/0.20), chela (without pedicel) 0.48 (0.48), hand (without pedicel) length 0.23 (0.22), movable finger length 0.25 (0.26). Carapace 0.47/0.41 (0.48‒0.39). Leg IV: femur + patella 0.27/0.11 (0.26/0.10), tibia 0.22/0.07 (0.21/0.06), tarsus 0.17/0.04 (0.16/0.04).
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- 2022
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19. Rhopalochernes catalinae Marimon & Blanco & Harvey 2022, sp. nov
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Marimon, Karla, Blanco, Eduardo Villarreal, and Harvey, Rk. S.
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Rhopalochernes catalinae ,Rhopalochernes ,Arthropoda ,Pseudoscorpiones ,Arachnida ,Chernetidae ,Animalia ,Biodiversity ,Taxonomy - Abstract
Rhopalochernes catalinae sp. nov. Figs. 4A–F, 5A–G, 6A–G, 7B ZooBank Registration: urn:lsid:zoobank.org:pub: 33CE2DF6-A490-4524-89DF-D6C5D5A884A7 Type material. female holotype: COLOMBIA, Atlántico, Municipio de Usiacurí, Reserva Campesina La Montaña (10°46’02,06” N, 75°02’34” W), 150m, 08.VI.2019, K. Marimon and E. Villarreal leg. (ICN-APs-843). Paratypes: 1 female and 3 males with the same data as the holotype (IAvH-I-3856 [2♂]; ICN-Aps-844 [1♂, 1♀]); 2 females and 2 males, Colombia, Atlántico, Municipio de Juan de Acosta, Corregimiento de Chorrera (10°47′48.34″ N, 75°00′45.37″ W), 270 masl. 09. VI.2018, K. Marimon, D. Tilano and E. Villarreal leg (IAvH-I-3846 [1♀]; ICN-Aps- 845 [1♀, 2♂]); 1 female, Colombia, Bolívar, Municipio de San Jacinto, Vereda La Flecha, Finca Amanecer Gaitero (9°51′9.74″ N; 75°10′32.32″ W), 250 masl. 11-12.IX.2019, K. Marimon & E. Villarreal leg. (ICN-APs-846). Etymology. This species is named for our colleague Catalina Romero-Ortiz, in appreciation of her research on Colombian pseudoscorpions. Diagnosis: Rhopalochernes catalinae sp. nov. can be distinguished from other species of the genus by the following combination of characters: cheliceral hand with four setae (Figs. 5E, 6E); serrula exterior with 11-12 blades; eyeless (Figs. 4C, 4F); carapace with shallow transverse furrows (only visible in lateral view); nodus ramosus at the same level or slightly close to st (Figs. 5G, 6G); and trichobothria st midway between t and sb (Figs. 5G, 6G). Differential diagnosis: Rhopalochernes catalinae sp. nov. can be differentiated from R. chamberlini, R. panamensis and R. ohausi by the lack of eyespots (Figs. 4C, 4F). It also differs from R. chamberlini by the thicker femur + patella of leg IV, 2.60‒2.89 versus 3.73 × longer than deep in R. chamberlini. It can be distinguished from R. panamensis and R. ohausi by the serrula exterior which has 11‒12 blades, but 14‒15 blades in R. panamensis and 16 blades in R. ohausi. It can also be distinguished from R. ohausi by having gaping chelal fingers (versus not gaping in R. ohausi, see Mahnert, 2001, Fig. 110). Rhopalochernes catalinae sp. nov. most closely resembles R. insulanus and R. luiscarlosi sp. nov. in the absence of eyes (Figs. 4C, 4F), but can be differentiated from R. insulanus by the number of setae on the cheliceral hand, 6 in R. insulanus versus 4 in R. catalinae sp. nov. and R. luiscarlosi sp. nov., a trait also found in R. chamberlini and R. panamensis (see Heurtault, 1998, Figs. 4 and 9). Rhopalochernes catalinae sp. nov. can also be distinguished from R. luiscarlosi sp. nov. by the shape of the furrows on the surface of the carapace, which are shallow and inconspicuous in R. catalinae sp. nov. (Figs. 4C, 4F), but are deep and conspicuous in R. luiscarlosi sp. nov. (Figs. 1C, 1F). They also differ in other features such as: the shape of the spermathecae, with short and thicker ducts (Fig. 7B) versus elongated and narrow ducts in R. luiscarlosi sp. nov. (Fig. 7A); the shape of tarsus IV, which is robust (2.75–3.75 × longer than deep) while that of R. luiscarlosi sp. nov. is slender (4.00–4.25 × longer than deep). Description of adult: Colour: Carapace reddish brown towards the anterior margin and lighter towards posterior margin, pedipalps reddish brown. Tergites and legs yellowish brown (Fig. 4). Carapace: heavily granulated; 1.24‒1.41 (♂) 1.24‒1.37 (♀) × longer than broad, eyes or eye‒spot absent; with 2 inconspicuous transverse furrows slightly visible on lateral view, posterior furrow closer to posterior margin than anterior furrow; posterior margin of carapace slightly v shaped; anterior margin with 6 setae (♂, ♀), posterior margin with 8‒9 setae (♂, ♀). (Fig. 4C, F) Chelicera: 1.43‒2.00 (♂), 1.33‒1.80 (♀) × longer than broad; hand with 4 setae (sbs absent) and 1 distal seta (gs) on movable finger, is, bs and es short and acuminate, ls longer and broad (Figs. 5E, 6E), galea with 4 rami (♀) or simple (♂) (Figs. 5C, 6D); rallum with 3 blades (Figs. 5D, 6C), anterior blade with several ramifications while others smooth; serrula exterior with 11‒12 blades (♂, ♀), lamina exterior present. Pedipalp: trochanter, femur, patella and hand heavily granulated, with short, feathered and acuminate setae (Figs. 5F, 6F), chelal fingers smooth; trochanter 1.20‒1.57 (♂), 1.20‒1.64 (♀), femur 2.07‒2.77 (♂), 2.43‒3.08 (♀), patella 1.62‒2.36 (♂), 1.93‒2.43 (♀), chela (with pedicel) 2.94‒3.27 (♂), 2.89‒3.24 (♀), chela (without pedicel) 2.40‒2.53 (♂), 2.45‒2.63 (♀). Hand 1.24‒1.40 (♂), 1.25‒1.41 (♀) × longer than broad, movable finger 1.10‒1.24 (♂), 1.09‒1.27 (♀) × longer than hand. All marginal teeth rounded except the terminal ones, which are pointed, accessory teeth not visible. Fixed chelal finger with 8 trichobothria. movable chelal finger with 4 trichobothria: eb, esb and est in the first half of fixed finger, esb closer to eb than est, which is closer to the midpoint of the finger, et distal and close to the fingertip; ib at the same level of eb, ist slightly aligned to esb, isb at the same level as st, close to est, it closer to et than isb; b and sb grouped basally, st and t in the middle of the movable finger, st slightly closer to t than sb, t much closer to st than tip of the finger. Venom apparatus present only in movable chelal finger with nodus ramosus at the same level or slightly close to st (Figs. 5G, 6G). Coxal region: maxillae smooth except for the antero-lateral region, coxae smooth, manducatory process triangular in shape with 2-3 apical setae, 1 prolateral suboral seta and 14-15 (♂), 11 (♀) additional setae on maxilla. Median maxillary lyrifissure rounded and situated submedially. Chaetotaxy of coxae I-IV, ♂, 7-8: 8-10: 8: 12; ♀, 9: 9: 12: 24. Legs: granulate, feathered setae on retrolateral margin and dentate setae on prolateral margins. Femur + patella of leg IV 2.25‒2.70 (♂), 2.60‒2.89 (♀) × longer than depth, as well as tibia and tarsus 2.71‒3.33 (♂), 3.17‒3.67 (♀) and 2.75‒3.75 (♂), 3.25‒3.75 (♀) × longer than broad, respectively. Tarsi III and IV with tactile seta, located subdistally. Arolium undivided, slightly shorter than claws, claws slender and simple, not modified (Figs. 5A‒B, 6A‒B). Abdomen: tergites I-X and sternites IV-X with a clear medial suture line (Fig. 7D). Tergal chaetotaxy: ♂, 12: 11-12: 11-13:15-16: 14-15: 15-16: 15-16: 14-16: 13-14: 12-13: 9-10: 2, ♀, 12: 14: 13: 16: 17: 18: 19: 16: 16: 13: 9: 2. Sternal chaetotaxy: ♂, (1) 4-6 (1): (1) 7-9 (1): 13-14: 12-13: 13: 13: 12: 10: 4-6: 2, ♀, 20: (1) 5 (1): (1) 15 (1): 15: 15: 14: 14: 14: 9: 16: 2. Tergites with setae acuminate, sternites with setae leaf-like shape. Pleural membrane striated and without setae. Genitalia: female: spermathecae paired, with short ducts ending in oval sacs (Fig. 7A). Male: genital opercula containing 18 setae on the anterior operculum and 4 in distal margin of posterior operculum. Dimensions: holotype female (ICN APs-843), with a range of 5 females paratype in parentheses: Body length 1.4 (1.04‒1.50). Pedipalps: trochanter 0.21/0.14 (0.21‒0.23/0.13‒0.15), femur 0.33/0.13 (0.33‒0.37/0.12‒0.14), patella 0.27/0.14 (0.27‒0.34/0.14‒0.15), chela (with pedicel) 0.51/0.16 (0.51‒0.55/0.16‒0.18), chela (without pedicel) 0.47 (0.46‒0.50), hand (without pedicel) length 0.2 (0.20‒0.24), movable finger length 0.25 (0.25‒0.28). Carapace 0.45/0.36 (0.45‒0.49/0.36‒0.39). Leg IV: femur + patella 0.25/0.09 (0.25‒0.27/0.09‒0.1), tibia 0.19/0.06 (0.19‒ 0.22/0.06), tarsus 0.14/0.04 (0.13‒0.15/0.04). Paratype male (ICN APs-844), with a range of 7 male in parentheses: Body length 1.34 (1.11‒1.35). Pedipalps: trochanter 0.21/0.14 (0.18‒0.22/0.14‒0.15), femur 0.36/0.13 (0.29‒0.38/0.13‒0.16), patella 0.33/0.15 (0.21‒ 0.34/0.13‒0.16), chela (with pedicel) 0.51/0.17 (0.48‒0.55/0.15‒0.18), chela (without pedicel) 0.46 (0.43‒0.49), hand (without pedicel) length 0.21 (0.21‒0.23), movable finger length 0.26 (0.23‒0.27). Carapace 0.47/0.35 (0.46‒ 0.48/0.34‒0.37). Leg IV: femur + patella 0.26/0.11 (0.25‒0.27/0.10‒0.12), tibia 0.19/0.07 (0.17‒0.22/0.06‒0.07), tarsus 0.14/0.04 (0.11‒0.15/0.04)., Published as part of Marimon, Karla, Blanco, Eduardo Villarreal & Harvey, Rk. S., 2022, Two new species of Rhopalochernes Beier, 1932 (Pseudoscorpiones: Chernetidae) from Colombia, pp. 397-410 in Zootaxa 5150 (3) on pages 403-407, DOI: 10.11646/zootaxa.5150.3.5, http://zenodo.org/record/6623085, {"references":["Heurtault, J. (1998) Pseudoscorpions of the genus Rhopalochernes (Chernetidae) from Panama and Venezuela. Journal of Arachnology, 26, 442 - 446."]}
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20. Two new species of Rhopalochernes Beier, 1932 (Pseudoscorpiones: Chernetidae) from Colombia
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Marimon, Karla, Blanco, Eduardo Villarreal, and Harvey, Rk. S.
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Arthropoda ,Pseudoscorpiones ,Arachnida ,Chernetidae ,Animalia ,Biodiversity ,Taxonomy - Abstract
Marimon, Karla, Blanco, Eduardo Villarreal, Harvey, Rk. S. (2022): Two new species of Rhopalochernes Beier, 1932 (Pseudoscorpiones: Chernetidae) from Colombia. Zootaxa 5150 (3): 397-410, DOI: https://doi.org/10.11646/zootaxa.5150.3.5
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21. Associated pseudoscorpions (Arachnida: Pseudoscorpiones) with waste heaps of Atta colombica (Guérin-Méneville, 1844) (Hymenoptera: Formicidae) in Panama
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Daniel Emmen, Ramy Jhasser Martínez, Dora Isabel Quirós, and Gabriel A. Villegas Guzmán
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Atta ,Panama ,biology ,Lustrochernes ,Host (biology) ,Science ,cheiridiidae ,Atta colombica ,Zoology ,General Medicine ,Hymenoptera ,biology.organism_classification ,symbiosis ,QL1-991 ,ant nests ,atemnidae ,Entire life cycle ,Cordylochernes ,chernetidae - Abstract
Waste heaps of Atta are host to an extraordinary diversity of myrmecophiles insects and other arthropods. In this study, the presence of four species of pseudoscorpions is recorded in two Atta colombica waste heaps in the years 2016 and 2017. Two of these species, Cordylochernes scorpioides and Lustrochernes carolinensis are new records in waste heaps and except for the deutonymphs of L.carolinensis, the others all stages of post-embryonic development were present in the studied heaps, which could indicate that these two species carry out their entire life cycle in these waste mounds and live there permanently.
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- 2021
22. Description of a new pseudoscorpion, Nudochernes limusensis sp. n. (Pseudoscorpiones: Chernetidae) from northern Iran, with a key to all Lamprochernetinae genera
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Mahrad Nassirkhani
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0106 biological sciences ,biology ,Genus ,010607 zoology ,Chernetidae ,Zoology ,Key (lock) ,Animal Science and Zoology ,Taxonomy (biology) ,biology.organism_classification ,010603 evolutionary biology ,01 natural sciences ,Pseudoscorpion - Abstract
The pseudoscorpion genus Nudochernes Beier, 1935 (Chernetidae) is reported from Iran for the first time, and a new species, Nudochernes limusensis sp. n. is described on the basis of two females co...
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- 2021
23. Nudochernes Beier 1935
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Xu, Hongru, Gao, Zhizhong, and Zhang, Feng
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Arthropoda ,Pseudoscorpiones ,Arachnida ,Chernetidae ,Nudochernes ,Animalia ,Biodiversity ,Taxonomy - Abstract
Genus Nudochernes Beier, 1935 Nudochernes Beier, 1935: 122; Beier, 1959: 48; Harvey, 1991: 607. Type species: Nudochernes montanus Beier, 1935, by original designation. Key to the Chinese species of Nudochernes 1. Pedipalpal femur 3.20 times longer than broad............................................ N. lipsae Mahnert, 2003 - Pedipalpal femur 2.40���2.90 times longer than broad.......................................................... 2 2. Trichobothria st closer to t than to sb; pedipalpal chela (with pedicel) 3.40���3.80 times longer than broad............................................................................................... N. troglobius Mahnert, 2009 - Trichobothria s t situated midway between sb and t; pedipalp chela (with pedicel) 3.10 (♂) 2.62���2.68 (♀) times longer than broad.......................................................................... N. pseudptroglobius sp. nov., Published as part of Xu, Hongru, Gao, Zhizhong & Zhang, Feng, 2022, Two new species of the pseudoscorpion subfamily Lamprochernetinae Beier, 1932 from Guizhou, China (Pseudoscorpiones: Chernetidae), pp. 581-592 in Zootaxa 5105 (4) on pages 582-587, DOI: 10.11646/zootaxa.5105.4.7, http://zenodo.org/record/6333898, {"references":["Mahnert, V. (2003) Four new species of pseudoscorpions (Arachnida, Pseudoscorpiones: Neobisiidae, Chernetidae) from caves in Yunnan Province, China. Revue suisse de Zoologie, 110 (4), 739 - 748. https: // doi. org / 10.5962 / bhl. part. 80209","Mahnert, V. (2009) New species of pseudoscorpions (Arachnida, Pseudoscorpiones, Chthoniidae, Chernetidae) from caves in China. Revue suisse de Zoologie, 116 (2), 185 - 201. https: // doi. org / 10.5962 / bhl. part. 79492"]}
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24. Nudochernes pseudotroglobius Xu & Gao & Zhang 2022, sp. nov
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Xu, Hongru, Gao, Zhizhong, and Zhang, Feng
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Arthropoda ,Pseudoscorpiones ,Arachnida ,Chernetidae ,Nudochernes ,Animalia ,Nudochernes pseudotroglobius ,Biodiversity ,Taxonomy - Abstract
Nudochernes pseudotroglobius sp. nov. (Figs 1–4) http://zoobank.org/NomenclaturalActs/ 20C7BD03-E125-4379-8D91-A3111A273DDF Type material. Holotype ♀ (Ps.- MHBU-GZXS202401): China, Guizhou Province, Xishui County, Daozuo Cave [28.511389°N, 107.153333°E], elev. 1601m a.s.l., 31 August 2020, Zegang Feng & Yanmeng Hou leg. Paratypes: 1♀ (Ps.- SWUC-GZXS202402), 1♂ (Ps.- MHBU-GZXS202403), same data as holotype. Etymology. The name refers to its similar habitat with Nudochernes troglobius Mahnert, 2009. Diagnosis. This species can be distinguished from other Nudochernes species by the presence of dentate setae on carapace and pedipalp, spermathecae with a long unpaired tube and two short apical tubules, st situated midway between sb and t, the presence of elongate setae on the posterior corners of coxae IV, and the tarsus IV with a tactile seta in middle of tarsus (TS=0.55 (♂) 0.57 (♀)). Description. (Fig. 2). Males smaller than females with 2.77 (♂) 3.11–3.16 (♀), carapace and pedipalps reddish brown, chelicera, sternites, tergites and legs yellowish brown. Carapace (Fig. 3A): evenly granulate; 1.12 (♂) 0.97–0.98 (♀) times longer than broad; eyes or eye-spots absent; with two distinct deep transverse furrows; subbasal transverse furrow situated closer to the posterior margin than to the median furrow; posterior area with a small longitudinal furrow; including 16 (♂) 10 (♀) setae on anterior margin and 15 (♂) 16 (♀) setae on posterior margin. Abdomen: all tergites and sternites narrowly divided (except the last one). Tergal chaetotaxy (I–XI): ♂, 7–7: 10–8: 8–7: 9–9: 8–8: 9–8: 9–9: 9–7: 7–7: 6–9: 11(2T); ♀, 7–7: 9–10: 9–8: 11–10: 10–10: 9–10: 9–10: 8–9: 7–8: 7–7: 10(2T); all setae clavate. Sternal chaetotaxy (IV–XI): ♂, 7–9: 11–11: 11–10: 9–10: 9–8: 8–8: 8–7: 10; ♀, 4–4: 6–6: 12–13: 13–12: 12–13: 13–13: 9–8: 11; all setae acuminate. Sternite II of ♀ with 18 setae arranged as an inverted “U” pattern (Figs 3E, 4E). Chelicerae (Figs 3D, 4D): 5 setae on hand and 1 subdistal seta on movable finger; sbs, bs, es dentate apically, ls, is, gs acuminate; fixed finger with 6 proximad-directed teeth, movable finger with broad tooth-like subapical lobe; galea with 6 long branchlets in distal part; rallum with 3 dentate blades (Fig. 4C); serrula exterior with 20 (♂, ♀) blades. Pedipalp (Figs 3B, 4A): pedipalp robust; trochanter, femur, patella and chelal hand coarsely granulate, with dentate setae; chelal fingers with short setae; trochanter 2.24 (♂) 1.50–1.62 (♀), femur 2.24 (♂) 2.33–2.61 (♀), patella 2.30 (♂) 2.12–2.38 (♀), chela (without pedicel) 2.71 (♂) 2.33–2.47 (♀), hand (without pedicel) 1.29 (♂) 1.21–1.26 (♀) times longer than broad, movable finger 1.27 (♂) 1.12–1.28 (♀) times as long as hand (without pedicel). Fixed chelal finger with 8 trichobothria, movable chelal finger with 4 trichobothria (Figs 3C, 4F): eb situated basally; est situated midway between esb and et; ib and esb situated sub-basally, it situated closer to tip of finger than to ib; s t situated midway between sb and t, sb situated closer to b than to s t, and t situated midway between tip of finger and st; fixed finger with 49 teeth, plus 5 prolateral accessory teeth and 5 retrolateral accessory teeth; movable finger with 47 teeth, plus 6 prolateral accessory teeth and 5 retrolateral accessory teeth. Venom apparatus only present in movable chelal finger, venom duct slender, nodus ramosus closer to t than to st. Coxae: with numerous short setae over entire ventral surface, with longer setae on posterior margin of coxae IV. Genitalia (Fig. 4B): ♂: typical of Chernetidae; ♀: spermathecae with a long unpaired tube and two short apical tubules. Legs I (Figs 3F, 4G): trochanter, femur, patella, tibia with numerous clavate setae; tarsus with numerous acuminate setae; proportions: trochanter 1.09 (♂) 1.20–1.31 (♀), femur 1.46 (♂) 1.51–1.84 (♀), patella 2.07 (♂) 2.09– 2.41 (♀), tibia 3.86 (♂) 3.33–3.70 (♀), tarsus 3.98 (♂) 4.30–5.01 (♀) times longer than wide; claws simple, arolium shorter than claws. Legs IV (Figs 3H, 4H): femur, patella, tibia with numerous clavate setae; trochanter and tarsus with numerous acuminate setae; proportions: trochanter 1.69 (♂) 1.65–1.77 (♀), femur + patella 5.50 (♂) 5.46–5.50 (♀), tibia 4.24 (♂) 4.58–5.10 (♀), tarsus 4.32 (♂) 4.20–4.87 (♀) times longer than deep, a tactile seta near middle of tarsus (Figs 3I, 4I) (TS=0.55 (♂) 0.57 (♀)); claws simple, arolium shorter than claws. Dimensions (length/breadth or depth, in mm). ♀: Total length 3.11–3.16. Carapace 0.70–0.76/0.71–0.78. Pedipalps: trochanter 0.41–0.42/0.25–0.31, femur 0.64–0.68/0.25–0.27, patella 0.64–0.68/0.25–0.29, chela (with pedicel) 1.14–1.31/0.36–0.42, chela (without pedicel) length 1.02–1.18, hand (without pedicel) length 0.48–0.53, movable finger length 0.54–0.68. Leg I: trochanter 0.17–0.18/0.13–0.15, femur 0.21–0.24/0.13–0.14, patella 0.23– 0.29/0.11–0.12, tibia 0.30–0.37/0.09–0.10, tarsus 0.30–0.35/0.07. Leg IV: trochanter 0.28–0.32/0.17–0.18, femur + patella 0.71/0.13–0.15, tibia 0.51–0.55/0.10–0.12, tarsus 0.39–0.42/0.08–0.10, TS=0.57. ♂: Total length 2.77. Carapace 0.72/0.64. Pedipalps: trochanter 0.40/0.22, femur 0.63/0.28, patella 0.65/0.28, chela (with pedicel) 1.15/0.37, chela (without pedicel) length 1.01, hand (without pedicel) length 0.48, movable finger length 0.61. Leg I: trochanter 0.15/0.14, femur 0.21/0.14, patella 0.25/0.12, tibia 0.33/0.09, tarsus 0.30/0.08. Leg IV: trochanter 0.26/0.15, femur + patella 0.59/0.11, tibia 0.42/0.10, tarsus 0.38/0.09, TS=0.55. Remarks. This new species is close related to N. troglobius Mahnert, 2009 (Hubei, China), but can be distinguished by the stouter pedipalp (chela (with pedicel) 3.10 (♂) 2.62–2.68 (♀) times longer than board versus 3.40–3.80 (♂, ♀) in N. troglobius) and the position of trichobothrium (s t situated midway between sb and t in N. pseudotroglobius sp. nov.; st closer to t than to sb in N. troglobius) (Mahnert 2009). This new species can be distinguished from N. lipsae Mahnert, 2003 (Yunnan, China) by the stouter legs I (patella 2.07 (♂) 2.09–2.41 (♀) times longer than deep vs 3.50 (♀) in N. lipsae; tibia 3.86 (♂) 3.33–3.70 (♀) times longer than deep vs 5.00 (♀) in N. lipsae), and by the position of trichobothrium (s t situated midway between sb and t in N. pseudotroglobius sp. nov., whereas s t closer to t than to sb in N. lipsae) (Mahnert 2003). Geographically, only one species, N. spalacis Beier, 1955, is described in Asia (Israel). The new species can be distinguished from N. spalacis by having slender legs IV (femur + patella 5.50 (♂) 5.46–5.50 (♀) times longer than deep versus 3.70 (♂) in N. spalacis) and the different position of trichobothrium (est situated midway between et and esb in N. pseudotroglobius sp. nov., whereas est closer to et than to esb in N. spalacis) (Beier 1955). Distribution. Known only from the type locality in Guizhou, China. Habitat. All specimens were collected under a rock within the dark zone of the cave.
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25. Megachernes biyunensis Xu & Gao & Zhang 2022, sp. nov
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Xu, Hongru, Gao, Zhizhong, and Zhang, Feng
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Arthropoda ,Pseudoscorpiones ,Megachernes ,Arachnida ,Chernetidae ,Animalia ,Megachernes biyunensis ,Biodiversity ,Taxonomy - Abstract
Megachernes biyunensis sp. nov. (Figs 5–7) http://zoobank.org/NomenclaturalActs/31be2f78-81ae-4bb7-aa18-076eb4722f89 Type material. Holotype ♀ (Ps.- MHBU-GZ19080501): China, Guizhou Province, Pan County, Biyun Park [25.775000°N, 104.638333°E], 5 August 2019, Zegang Feng & Zhaoyi Li leg. Paratypes: 1♀ (Ps.-SWUC-GZ19080502); 1♂ (Ps.- MHBU-GZ19080503), same data as holotype. Etymology. The specific name refers to the type locality, Biyun Park, Pan County, Guizhou Province, China. Diagnosis. This new species can be recognized by the following combined characters: subbasal transverse furrow on carapace located midway between posterior margin and central furrow, the trichobothria st situated closer to sb than to t, t situated midway between tip of finger and st. Description. (Fig. 5). Carapace, chelicera, tergites and sternites yellowish brown, pedipalps reddish brown, colour of chelal hand darker than that of trochanter, femur and patella; soft parts pale. Carapace (Fig. 6A): evenly granulate; 1.07 (♂) 1.02 (♀) times longer than broad; eyes or eye-spots absent; with two distinct deep transverse furrows, subbasal transverse furrow situated midway between posterior margin and central furrow; posterior area with a small longitudinal furrow; with numerous setae including 16 (♂) 20 (♀) acuminate setae on anterior margin and 10 (♂) 14 (♀) on posterior margin. Abdomen: all tergites and sternites narrowly divided. Tergal chaetotaxy (I–XI): ♂, 7–6: 10–8: 7–8: 7–8: 7–8: 9– 8: 9–9: 7–9: 8–6: 7–8: 6(2 T)–7(2T); ♀, 7–7: 9–8: 8–8: 9–9: 9–8: 8–9: 8–9: 8–9: 9–7: 7–8: 7(2 T)–7(2T); I–X tergites with paired dark spot. Sternal chaetotaxy (IV–XI): ♂, 4–5: 8–9: 13–11: 13–12: 10–11: 11–19: 11–9: 6(2 T)–7(2T); ♀, 4–3: 10–12: 14–12: 14–14: 13–14: 12–14: 12–12: 6(2 T)–6(2 T); all sternal setae acuminate. Sternite II of ♀ with 33 setae arranged in a cluster (Figs. 6E, 7F). Chelicerae (Figs. 6D, 7D): 7 setae on hand and 1 subdistal seta on movable finger; basal 5 setae finely dentate apically, ls, is and gs acuminate; fixed finger with 3 proximad-directed teeth; galea comprising 2 parts, first part with 5 branches and the second with 4 branches (Fig. 7B). Serrula exterior with 27 (♂, ♀) blades; rallum with 3 dentate blades, the apex of the first one slightly twisted and with anterior margin dentate, the other two blades apically dentate (Fig. 7C). Pedipalp (Figs 6B, 7A): trochanter, femur, patella and chelal hand coarsely granulate, with acuminate setae; chelal fingers with short setae; trochanter 1.39 (♂) 1.67 (♀), femur 2.51 (♂) 2.31 (♀), patella 2.26 (♂) 2.23 (♀), chela (without pedicel) 3.02 (♂) 2.81 (♀), hand (without pedicel) 1.58 (♂) 1.51 (♀) times longer than board, movable finger 0.91 (♂) 0.96 (♀) times as long as hand (without pedicel). Fixed finger with 8 trichobothria, movable finger with 4 trichobothria (Figs 6C, 7E): eb situated basally; est situated closer to esb than to et; ib and esb situated sub-basally; it situated closer to tip of finger than to ib; st situated closer to sb than to t, sb situated closer to s t than to b, and t situated midway between tip of finger and st, fixed finger with 68 teeth, plus 13 prolateral accessory teeth, and 8 retrolateral accessory teeth; movable finger with 59 teeth, plus 12 prolateral accessory teeth, and 7 retrolateral accessory teeth. Venom apparatus only present in movable chelal finger, venom duct slender, nodus ramosus closer to t than to st. Coxae: with numerous short setae over entire ventral surface and with long setae on posterior margin of coxae IV; posterior corner of coxae IV slightly protruding. Genitalia (Figs 6E, 7H): ♂: typical of Chernetidae; ♀: spermathecae T-shaped and with extremely elongated ends. Leg I (Figs 6F, 7G): with long acuminate setae; proportions: trochanter 1.11 (♂, ♀), femur 1.50 (♂) 1.51 (♀), patella 2.60 (♂) 2.17 (♀), tibia3.71 (♂) 3.50 (♀), tarsus 4.41 (♂) 4.10 (♀) times longer than deep; claws simple, arolium shorter than claws. Legs IV (Figs 6H, 7I): with long acuminate setae; proportions: trochanter 1.76 (♂) 1.44 (♀), femur + patella 3.96 (♂) 3.43 (♀), tibia 5.01 (♂) 4.71 (♀), tarsus 3.80 (♂) 3.83 (♀) times longer than deep; tactile seta in middle tarsus (TS=0.51 (♂) 0.54 (♀)), length of tactile seta 2/3 of tarsus (Fig. 7J); claws simple, arolium shorter than claws. Dimensions: (length/breadth or depth, in mm). ♀: Total length 4.22. Carapace 1.20/1.18. Pedipalps: trochanter 0.65/0.39, femur 0.99/0.43, patella 1.07/0.48, chela (with pedicel) 1.95, chela (without pedicel) 1.80, hand (without pedicel) length 0.97, movable finger length 0.94. Leg I: trochanter 0.21/0.18, femur 0.30/0.21, patella 0.39/0.18, tibia 0.49/0.14, tarsus 0.41/0.10. Leg IV: trochanter 0.36/0.25, femur + patella 0.79/0.23, tibia 0.80/0.17, tarsus 0.46/0.12, TS=0.54. ♂: Total length 4.10. Carapace 1.14/1.05. Pedipalps: trochanter 0.59/0.43, femur 1.05/0.41, patella 1.06/0.47, chela (with pedicel) 1.93/0.64, chela (without pedicel) length 1.87, hand (without pedicel) length 1.01, movable finger length 0.92. Leg I: trochanter 0.22/0.20, femur 0.36/0.24, patella 0.52/0.2, tibia 0.51/0.14, tarsus 0.48/0.11. Leg IV: trochanter 0.36/0.21, femur + patella 1.06/0.27, tibia 0.81/0.16, tarsus 0.57/0.15, TS=0.51. Remarks. Based on the key of Megachernes species (Mahrad & Reza 2017), this new species is similar to M. limatus Hoff & Parrack, 1958 from Oceania, but can be distinguished by the character of carapace (the subbasal transverse furrow situated closer to the posterior margin than to the median furrow in M. limatus, whereas the subbasal transverse furrow situated midway in M. biyunensis sp. nov.); and by the different trichobothrial pattern (st situated closer to sb than to t in M. biyunensis sp. nov., whereas st is closer to t than to sb in M. limatus) (Hoff & Parrack 1958). It can be distinguished from M. himalayensis (Ellingsen, 1914) (China (Fujian); India; Nepal) by the number of accessory teeth on the chelal fingers (movable finger with 12 accessory teeth and fixed finger with 13 accessory teeth in M. biyunensis sp. nov., whereas movable finger with 6 accessory teeth and fixed finger with 9 accessory teeth in M. himalayensis); and by the stouter legs IV (tibia 5.01 (♂) 4.71 (♀) times longer than deep versus 6.20 (♀) in M. himalayensis; tarsus 3.80 (♂) 3.83 (♀) times longer than deep vs 5.00 (♀) in M. himalayensis) (Ellingsen 1914). It can be distinguished from M. titanius Beier, 1951 (China (Sichuan, Guangxi); Southeast Asia) by the trichobothrial pattern (st situated closer to sb than to t in M. biyunensis sp. nov., whereas st is closer to t than to sb in M. titanius); and by the stouter legs IV (5.01 (♂) 4.71 (♀) times longer than wide versus 6.20 (♀) in M. titanius; tarsus 3.80 (♂) 3.83 (♀) times longer than deep versus 5.20 (♀) in M. titanius) (Beier 1951). It differs from M. tuberosus Mahnert, 2009 (Sichuan, China) by different the trichobothrial pattern (st situated closer to sb than to t in M. biyunensis sp. nov., whereas st is closer to t than to sb in M. tuberosus); and by the morphology of the rallum (all three blades denticulate in M. biyunensis sp. nov., blades terminally scarcely dentate and apex of first blade slightly twisted in M. tuberosus) (Mahnert 2009). It differs from M. vietnamensis Beier, 1967 (China (Sichuan, Hubei, Yunnan); Vietnam) by the number of accessory teeth on the chelal fingers (movable finger with 12 accessory teeth and fixed finger with 13 accessory teeth in M. biyunensis sp. nov., whereas fixed finger with 21 accessory teeth in M. vietnamensis); and by the cheliceral hand setae (basal 5 setae with terminally dentateand acuminate in M. biyunensis sp. nov., whereas all setae with acuminate in M. vietnamensis) (Beier 1967). Distribution. Known only from the type locality, Guizhou, China. Habitat. All specimens were collected in wet leaf litter under Populus (Salicaceae).
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26. Megachernes Beier 1932
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Xu, Hongru, Gao, Zhizhong, and Zhang, Feng
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Arthropoda ,Pseudoscorpiones ,Megachernes ,Arachnida ,Chernetidae ,Animalia ,Biodiversity ,Taxonomy - Abstract
Genus Megachernes Beier, 1932 Megachernes Beier, 1932: 128; Beier, 1933: 518; Beier, 1948: 476; Morikawa, 1960: 144; Harvey, 1991: 599. Type species: Chernes grandis Beier, 1930, by original designation. Key to the Chinese species of Megachernes 1. Leg IV femur + patella with numerous glandular microsetae........................... M. glandulosus Mahnert, 2009 - Leg IV femur + patella without glandular microsetae......................................................... 2 2. Male pedipalpal patella with hump................................................. M. tuberosus Mahnert, 2009 - Male pedipalpal patella without hump..................................................................... 3 3. Pedipalpal femur less than 4.00 times longer than board....................................................... 4 - Pedipalpal femur more than 4.00 times longer than board..................................... M. titanius Beier, 1951 4. Leg IV femur + patella more than 4.00 times longer than deep.................................................. 5 - Leg IV femur + patella less than 4.00 times longer than deep................................................... 6 5. Movable chelal finger with 9 retrolateral accessory teeth; all blades of rallum smooth..... M. himalayensis (Ellingsen, 1914) - Movable chelal finger with 21 retrolateral accessory teeth; only distal blade of rallum denticulate.................................................................................................... M. vietnamensis Beier, 1967 6. Only distal blade of rallum denticulate; st situated closer to t than to sb........................ M. grandis (Beier, 1930) - All blades of rallum denticulate; st situated closer to sb than to t................................ M. biyunensis sp. nov., Published as part of Xu, Hongru, Gao, Zhizhong & Zhang, Feng, 2022, Two new species of the pseudoscorpion subfamily Lamprochernetinae Beier, 1932 from Guizhou, China (Pseudoscorpiones: Chernetidae), pp. 581-592 in Zootaxa 5105 (4) on pages 587-591, DOI: 10.11646/zootaxa.5105.4.7, http://zenodo.org/record/6333898, {"references":["Beier, M. (1932) Pseudoscorpionidea II. Subord. C. Cheliferinea. Tierreich, 58, i - xxi + 1 - 294. https: // doi. org / 10.1515 / 9783111385402","Mahnert, V. (2009) New species of pseudoscorpions (Arachnida, Pseudoscorpiones, Chthoniidae, Chernetidae) from caves in China. Revue suisse de Zoologie, 116 (2), 185 - 201. https: // doi. org / 10.5962 / bhl. part. 79492","Beier, M. (1951) Die Pseudoscorpione Indochinas. Memoires du Museum National d'Histoire Naturelle, Paris, Nouvelle Serie, 147 - 123.","Beier, M. (1967) Pseudoscorpione vom kontinentalen Sudost-Asien. Pacific Insects, 9, 341 - 369."]}
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27. Two new species of the pseudoscorpion subfamily Lamprochernetinae Beier, 1932 from Guizhou, China (Pseudoscorpiones: Chernetidae)
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HONGRU XU, ZHIZHONG GAO, and FENG ZHANG
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China ,Arthropoda ,Pseudoscorpiones ,Arachnida ,Chernetidae ,Animals ,Animalia ,Animal Science and Zoology ,Biodiversity ,Ecology, Evolution, Behavior and Systematics ,Taxonomy - Abstract
Two new species of the pseudoscorpion subfamily Lamprochernetinae Beier, 1932 are described from Guizhou Province, China, Nudochernes pseudotroglobius sp. nov. and Megachernes biyunensis sp. nov., with detailed diagnoses, descriptions and illustrations.
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28. Soil and canopy Pseudoscorpiones (Arthropoda, Arachnida) in a monodominant forest of Attalea phalerata Mart. (Arecaceae) in the Brazilian Pantanal.
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Battirola, Leandro D., Brizzola dos Santos, Geane, Meurer, Eliandra, Castilho, Augusto C. C., Mahnert, Volker, Brescovit, Antonio D., and Marques, Marinêz Isaac
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PSEUDOSCORPIONS , *FOREST litter , *ATTALEA , *PLANT canopies , *CHERNETIDAE - Abstract
We studied the occurrence of Pseudoscorpiones in the soil, leaf litter, and in canopies of a monodominant forest ofAttalea phalerataat different seasons in the northern region of the Brazilian Pantanal. A total of 1197 pseudoscorpions from nine families and 16 species were sampled. Olpiidae, Chernetidae, and Geogarypidae predominated in soil and leaf litter. Chernetidae was the most abundant family in canopies. Soil and canopy corresponded to distinct habitats in relation to pseudoscorpion abundance and richness, with the canopies being the most diversified environment. These habitats are occupied in different ways by pseudoscorpion populations.Geogarypussp. occurs in the edaphic environment during receding water and dry season, but can be found in canopies ofA. phalerataexclusively during high water. This alternation in the use of the edaphic environments and canopies in the same area by pseudoscorpion species probably happens due to the strong seasonality of the Brazilian Pantanal. [ABSTRACT FROM PUBLISHER]
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29. First record of phoresy of Dendrochernes cyrneus (L. Koch, 1873) (Pseudoscorpiones, Chernetidae) on Cerambyx cerdo Linnaeus, 1758 (Coleoptera, Cerambycidae) and their potential value as bioindicators.
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Karpiński, L., Rutkowski, T., and Szczepański, W. T.
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CERAMBYCIDAE ,CHERNETIDAE ,PHORESY ,BIOINDICATORS ,SPECIES - Abstract
Copyright of Animal Biodiversity & Conservation is the property of Museu de Ciencies Naturals de Barcelona and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)
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30. Vertical and time distribution of Pseudoscorpiones (Arthropoda: Arachnida) in a floodplain forest in the Brazilian Pantanal.
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Dênis Battirola, Leandro, Henrique Rosado-Neto, Germano, Augusto Batistella, Daniel, Mahnert, Volker, Brescovit, Antonio Domingos, and Isaac Marques, Marinêz
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PSEUDOSCORPIONS , *FLOODPLAIN forests , *FOREST litter , *FOREST ecology , *FOREST canopies - Abstract
Pseudoscorpions embrace a diverse group of arachnids with approximately 3 500 species that occur in various habitats, such as soil, leaf litter, caves and canopies. This study aimed at evaluating the relationship between the pseudoscorpion assemblages in soil, termite nests, tree trunks and canopies, as well as the temporal distribution as to the abundance and richness of species in these habitats. For this purpose different sampling techniques were applied in an integrated manner in distinct habitats of a seasonally flooded monodominant forest in the Northern Pantanal of Mato Grosso, Brazil. Data regarding the abundance and richness of assemblage species were organized by means of the Non-Metric Multidimensional Scaling (NMDS). A total of 2 068 Pseudoscorpiones distributed in seven families and 18 species were captured. Chernetidae (8 spp.) and Withiidae (5 spp.) predominated, while Atemnidae, Cheiridiidae, Geogarypidae, Lechytiidae and Olpiidae were present with only one species each. Terrestrial fauna was more abundant (1 035 ind.; 50.0 % of the total catch) with three families and 10 species. In the arboreal fauna (712 ind.; 34.4 %), four families and 13 species were found. Termite mounds (321 ind.; 15.6 %) corresponded to the habitat with the least number of individuals, however, five families and nine species were identified, including Parachernes sp. 2, Geogarypus sp. and Olpiolum sp., not found in other analyzed habitats in this forest. The analyses did not show any temporal variation as to abundance or richness of Pseudoscorpiones in each evaluated habitat; however, the analysis showed that the edaphic environment (soil + termite nests), tree trunks and tree canopies are distinct habitats in relation to the composition of the assemblage. The occurrence of typical terricolous (e.g. Parawithius sp., Withiidae gen. sp. and Parachernes sp.) and other arboricolous (e.g. Cheiridium sp., Americhernes sp. and Lustrochernes sp.) species highlights the vertical stratification of the assemblage present in this floodplain forest in the Pantanal of Mato Grosso. [ABSTRACT FROM AUTHOR]
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31. NEW DATA CONCERNING THE DISTRIBUTION OF PSEUDOSCORPIONS IN ALBANIA (PSEUDOSCORPIONES: CHERNETIDAE).
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CHRISTOPHORYOVÁ, JANA and JABLONSKI, DANIEL
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PSEUDOSCORPIONS ,CHERNETIDAE ,ANIMAL species ,ARACHNIDA ,SPECIES - Abstract
Copyright of Natura Croatica is the property of Natura Croatica and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)
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32. A multivariate study of differentiating characters between three European species of the genus Lasiochernes Beier, 1932 (Pseudoscorpiones, Chernetidae).
- Author
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Christophoryová, Jana, Krajcovicová, Katarína, Henderickx, Hans, and Španiel, Stanislav
- Subjects
- *
PSEUDOSCORPIONS , *CHERNETIDAE , *MOLES (Animals) , *CAVES , *MORPHOMETRICS , *TAXONOMY - Abstract
Morphological variation in three rarely collected European species of the genus Lasiochernes Beier, 1932 is thoroughly examined in the present study. Detailed descriptions of previously ignored morphological characters of L. cretonatus Henderickx, 1998, L. jonicus (Beier, 1929) and L. pilosus (Ellingsen, 1910) are presented. he female of L. cretonatus and the nymphs of L. pilosus are described for the first time. Multivariate morphometric techniques (principal coordinate analysis and discriminant analyses) were employed to confirm morphological differentiation of the three Lasiochernes species and to identify the most reliable characters for their separation. he usefulness of particular body parts for species identification was evaluated. An identification key for the females of the Lasiochernes species studied is provided. Geographic distribution and habitat preferences of the three species are summarized. [ABSTRACT FROM AUTHOR]
- Published
- 2016
- Full Text
- View/download PDF
33. New cases of social parasitism among pseudoscorpions from Colombian populations.
- Author
-
Lacava, M., González-Gómez, J.C., Valenzuela-Rojas, J.C., Moncayo, C., Cardozo, L., Tizo-Pedroso, E., and García, L.F.
- Subjects
- *
PARASITISM , *PSEUDOSCORPIONS , *FORAGING behavior , *ANELOSIMUS studiosus , *PREDATION , *MORPHOMETRICS , *REGRESSION analysis , *HYMENOPTERA - Abstract
Social parasitism is more commonly found among the Hymenoptera. However, a recent study reported a case of parasitism between Neotropical pseudoscorpion species. Here, we extend the knowledge about this relationship, adding information about the species from Colombia. Sampling ofParatemnoides nidificatorcolonies in a secondary dry forest revealed the presence of two other species of pseudoscorpions also sharing the nest of the host. We presented data about the occurrence ofParachernes melanopygusand a second inquiline species of genusLustrochernes(both Chernetidae) and how they affect the host species. Aspects of the species ecology and behaviour are discussed. [ABSTRACT FROM AUTHOR]
- Published
- 2016
- Full Text
- View/download PDF
34. First record of phoretic association between Cordylochernes scorpioides (Linnaeus) (Pseudoscorpiones: Chernetidae) and Hylettus coenobita (Erichson) (Coleoptera: Cerambycidae) in central Amazon
- Author
-
Matheus Mickael Mota Soares, Fabián García, and Marcus Bevilaqua
- Subjects
phoresis ,biology ,Amazon rainforest ,Coenobita ,neotropical ,Chernetidae ,Zoology ,General Medicine ,pseudoscorpions ,biology.organism_classification ,Pseudoscorpion ,longhorn beetles ,south america ,Genus ,Phoresis ,lcsh:Zoology ,Hylettus ,dispersion ,lcsh:Q ,lcsh:QL1-991 ,lcsh:Science ,Longhorn beetle - Abstract
We herein report for the first time the phoretic association between the pseudoscorpion Cordylochernes scorpioides (Linnaeus, 1758) (Chernetidae) and the longhorn beetle Hylettus coenobita (Erichson, 1847) (Cerambycidae) in the central Amazon. In addition, this is the first record of pseudoscorpion phoresy for the genus Hylettus Bates, 1864.
- Published
- 2020
35. Chernes similis (Beier, 1932) (Pseudoscorpiones, Chernetidae) new to the fauna of Lithuania
- Author
-
Jana Christophoryová, Jolanta Rimsaite, Katarína Krajčovičová, and Povilas Ivinskis
- Subjects
Ecology ,biology ,botanical garden ,QH301-705.5 ,Fauna ,Chernetidae ,Zoology ,Baltic ,biology.organism_classification ,Geography ,distribution ,faunistics ,new record ,Biology (General) ,Ecology, Evolution, Behavior and Systematics - Abstract
The pseudoscorpion Chernes similis (Beier, 1932) is reported from the Baltic region for the first time. The new recordfrom Lithuania is based on a single male specimen found in a mould growing in a hollow of a Tilia L. tree in theBotanical Garden of Vilnius University. This finding represents the northernmost record of C. similis. With the newrecord of C. similis, nine pseudoscorpion species, belonging to six genera and three families, are currently known fromLithuania.
- Published
- 2020
36. First report the genus Dendrochernes Beier, 1932 (Pseudoscorpiones: Chernetidae) from China, with description of a new species
- Author
-
Feng. Zhang and Zhizhong. Gao
- Subjects
Geography ,biology ,Genus ,Insect Science ,Chernetidae ,Zoology ,biology.organism_classification ,China ,Ecology, Evolution, Behavior and Systematics - Published
- 2020
37. Pachychernes zehorum Muchmore 1997
- Author
-
Marimon, Karla, Villarreal-Blanco, Eduardo, Romero-Ortiz, Catalina, and Gutierrez, Luis C.
- Subjects
Arthropoda ,Pseudoscorpiones ,Pachychernes ,Arachnida ,Chernetidae ,Pachychernes zehorum ,Animalia ,Biodiversity ,Taxonomy - Abstract
Pachychernes zehorum Muchmore, 1997 Figs. 4A–D, 5A–G, 6A–G, 7B Pachychernes zehorum Muchmore, 1997: 19–21, figs 1–4; Ceballos, 2004: 429; Villegas-Guzman, 2006: 133; Harvey 2013. Diagnosis. This species differs from all other Pachychernes species by the first leg of the males, which not only has long and short modified setae on the tibia, but also a conspicuous depression on the dorsal side of the tarsus (Muchmore 1997) (Fig. 4). Examined material. COLOMBIA, Bolívar, Municipio de San Jacinto, La Flecha, Finca Amanecer Gaitero (9°51'9.74" N; 75°10'32.32" W), 250 m, 4 ♀ (ICN-Aps-835) and 2 ♂ (IAvH-I-4079), 11–12.IX.2019, K. Marimon and E. Villarreal leg. Description (adults): Colour: carapace red-brown with a lighter tone below the transversal furrow. Tergites light brown, pedipalps reddish-brown. Legs light yellow-brown toned. Carapace: heavily granulated, subrectangular with broad posterior margin; 0.78–0.93 (♂) 0.86–1.13 (♀) × longer than broad, with two eye spots; anterior margin with 8 setae (♂) 7 setae (♀), posterior margin with 6 setae (♂, ♀). Chelicera: 2.13–2.54 (♂), 1.44–2.40 (♀) × longer than broad; with 5 setae on hand and 1 distal seta on movable finger, es, is and ls acuminate, bs and sbs dentate; galea with 5 rami; rallum with 3 blades, posterior blade with several ramifications while others smooth; serrula exterior with 24 blades (♂, ♀); lamina exterior present (Figs. 5, 6). Pedipalp: with robust trochanter, femur, patella and granulated hand with several denticulated setae and chelal fingers smooth; trochanter 1.30–1.36 (♂), 1.27–1.39 (♀), femur 2.70–2.92 (♂), 2.10–2.42 (♀), patella 2.38–2.50 (♂), 2.12–2.37 (♀), chela (with pedicel) 2.81–3.05 (♂), 2.61–2.89 (♀), chela (without pedicel) 2.63–2.86 (♂), 2.61–2.89 (♀), hand 1.53–1.63 (♂), 1.54–1.68 (♀) × longer than broad, movable finger 0.76–0.77 (♂), 0.59–0.86 (♀) × longer than hand. All marginal teeth rounded except the terminal ones, which are pointed, external accessory teeth present on both fingers, with 6 (♂), 7 (♀) on the movable finger and 9 (♂), 11(♀) on the fixed finger. Fixed chelal finger with 8 trichobothria, movable chelal finger with 4 trichobothria: eb, esb, est and et slightly L-shaped, eb and esb situated basally, est located medially and at an equal distance from esb and et, which is located terminally; ib and ist basally located, with ist, eb and esb aligned, isb located in a medial position and closer to it and ib; b, sb and st placed in the first half of the movable finger with b and sb much closer to each other than to st, t located subterminally, midway from st and tip of finger. Venom apparatus present only in movable chelal finger with nodus ramosus located next to t (Figs. 5, 6). Coxal region: maxillae smooth except for the antero-lateral region, coxae smooth, manducatory process triangular in shape; regarding the setae, these individuals have one apical, one subapical and one sub oral while there are 25 additional setae (♂). Maxillary lyrifissure rounded and placed submedially. Chaetotaxy of coxae I–IV in ♂: 14: 12: 16: 44; ♀: 13: 11: 15: 36. Legs: leg I sexually dimorphic, with males having a tibia with a large number of setae plus a distinct depression on the surface of the tarsus while that of the females are chernetid in structure. Femur + patella of leg IV 2.67–2.77 (♂), 3.56–4.17 (♀) × longer than broad, as well as tibia and tarsus 3.79–4.11 (♂), 3.56–4.17 (♀) and 4.27–4.64 (♂), 3.89–4.67 (♀) × longer than broad, respectively. Tarsi III and IV with tactile seta, located subbasally, TS= 0.18 in both males and females approximately. Claws and arolium are equal in length. Abdomen: tergites I–X and sternites I–X with a clear medial suture line. Tergal chaetotaxy: ♂, 8: 7: 9: 8: 11: 13: 12: 12: 13: 12: 11: 2; ♀, 10: 10: 10: 10: 12: 12: 12: 13: 14: 13: 11: 2, all setae clavate. Sternal chaetotaxy: ♂, 47, (3) 16 (3): (1) 8 (1): 17: 19: 19: 23: 20: 17: 15: 2; ♀, 38: (2) 8 (2): (1) 9 (1): 20: 19: 18: 18: 18: 17: 16: 4. Spiracle with helix. Pleural membrane striated and without setae. Genitalia: spermatheca somewhat H-shaped, with four lobes, the anterior ones, oval in shape while the posterior ones have a tubular form with several cribriform plates along the ducts (Fig. 7B). Male genitalia consisting of 47 setae on the anterior operculum and 16 on the posterior operculum. Dimensions (mm): males, followed by females in parentheses: Body length 3.05–3.10 (2.44–3.30). Carapace 0.86–1.09/1.10–1.17 (0.81–1.05/0.82–1.22) Chelicera 0.32–0.33/0.13–0.15 (0.23–0.31/0.10–0.16), movable finger length 0.23–0.28 (0.20–0.25. Pedipalps: trochanter 0.48–0.49/0.36–0.37 (0.33–0.46/0.26–0.36), femur 1.10–1.14/0.37–0.39 (0.61–0.87/0.29–0.39), patella 1.00–1.15/0.42–0.46 (0.72–0.97/0.34–0.45), chela (with pedicel) 1.74/0.57–0.62 (1.39–1.89/0.46–0.62), chela (without pedicel) 1.63 (1.31–1.79), hand (without pedicel) length 0.93–0.95 (0.71–1.00), movable finger length 0.72 (0.57–0.85). Leg IV: femur 0.35–0.37/0.27–0.30 (0.26– 0.32/0.19–0.25), patella 0.77–0.8/0.35–0.36 (0.51–0.73/0.20–0.33), tibia 0.72–0.78/0.19 (0.50–0.72/0.12–0.18) tarsus 0.47–0.51/0.11 (0.35–0.49/0.09–0.11). Distribution and habitat. This species has been previously recorded from Mexico and Panama (Muchmore 1997; Ceballos 2004; Villegas-Guzman 2006), and according to Muchmore (1997) it is probably widespread through Central America. Here we expand the distribution to South America, with a population found in the Montes de María in northern Colombia. The new records demonstrate that this species is not necessarily restricted to environments such as rain forest (type locality) but also occurs in tropical dry forest (Figs. 8, 9)., Published as part of Marimon, Karla, Villarreal-Blanco, Eduardo, Romero-Ortiz, Catalina & Gutierrez, Luis C., 2021, A new species and new records of Pachychernes Beier, 1932 from Colombia (Pseudoscorpiones, Chernetidae), pp. 363-376 in Zootaxa 4999 (4) on pages 369-375, DOI: 10.11646/zootaxa.4999.4.6, http://zenodo.org/record/5119308, {"references":["Muchmore, W. (1997) An unusual new Pachychernes from Panama and Mexico (Pseudoscorpionida: Chernetidae). Entomological News, 108, 19 - 23.","Harvey, M. (2013) Pseudoscorpions of the world. Pseudoscorpions of the World, version 3.0. Western Australian Museum, Perth. Available from: http: // www. museum. wa. gov. au / catalogues / pseudoscorpions (accessed 25 February 2021)"]}
- Published
- 2021
- Full Text
- View/download PDF
38. A new species and new records of Pachychernes Beier, 1932 from Colombia (Pseudoscorpiones, Chernetidae)
- Author
-
Eduardo Villarreal-Blanco, Catalina Romero-Ortiz, Karla Marimon, and Luis Carlos Gutierrez
- Subjects
Male ,0106 biological sciences ,Arthropoda ,Pseudoscorpiones ,Chernetidae ,010607 zoology ,Zoology ,Colombia ,010603 evolutionary biology ,01 natural sciences ,Genus ,Arachnida ,Animals ,Animalia ,Ecology, Evolution, Behavior and Systematics ,Taxonomy ,Sex Characteristics ,biology ,Biodiversity ,biology.organism_classification ,Sexual dimorphism ,Key (lock) ,Female ,Animal Science and Zoology ,Taxonomy (biology) ,Animal Distribution - Abstract
In Colombia, the status of the Neotropical genus Pachychernes Beier, 1932 is unknown. The only available data in literature to support the presence of this genus is an adult of P. aff. subrobustus, possibly female, from copal resin without specific locality data, and a record at generic level from Northern Colombia. In this study, we extend the distribution of Pachychernes by describing a new species, P. florezi sp. n. and several reporting individuals of P. zehorum Muchmore, 1997 from Montes de María and the Caribbean coast of the country. These species are clearly differentiated from one another by the sexual dimorphism in the latter species, with a depression on the tarsus I in males. We also present an updated key for all species of the genus.
- Published
- 2021
39. PHORETIC RELATIONSHIP BETWEEN LUSTROCHERNES GROSSUS (PSEUDOSCORPIONIDA: CHERNETIDAE) AND ODONTOTAENIUS STRIATOPUNCTATUS (COLEOPTERA: PASALIDAE).
- Author
-
CASTILLO, María Luisa and VILLEGAS-GUZMÁN, Gabriel A.
- Subjects
- *
CHERNETIDAE , *PSEUDOSCORPIONS , *PASSALIDAE , *BEETLES , *PHORESY , *INSECT societies , *FUNGI - Abstract
Phoresy is considered a non-parasitic partnership between a small animal (phoront) and a large one (host) that result in phoront transportation by the host. Throughout two years of observation and nursing of 16 family groups of the passalid Odontotaenius striatopunctatus, we noticed the presence of the pseudoscorpion Lustrochernes grossus within 11 of their 16 nests, which consisted of rotten wood logs (30 cm long x 15-20 cm in diameter) cut into 2 cm segments and secured with rubber bands to facilitate observation. The presence of pseudoscorpions became evident from the moment the passalids started building their nests creating space and food for their young. Evidence was found that pseudoscorpions can go under the elytra of passalids. Their presence did not prevent the reproduction of the beetles, performed in 13 of the 16 set nests (Fischer's exact test: P = 0.71, N = 16): neither was the number of passalids offspring modified (Mann Whitney U = 11.50, P = 0.2553). On three occasions during spring, L. grossus females carrying brood sac was documented. In this facultative relationship, phoresy and phagophilia could be involved; some hypotheses on the factors that may interfere with it are posed. [ABSTRACT FROM AUTHOR]
- Published
- 2016
- Full Text
- View/download PDF
40. Neochelanops michaelseni (Pseudoscorpiones: Chernetidae) as a potential bioindicator in managed and unmanaged Nothofagus forests of Tierra del Fuego.
- Author
-
Lencinas, María Vanessa, Kreps, Gastón, Soler, Rosina, Peri, Pablo Luis, Porta, Andrés, Ramírez, Martín, and Pastur, Guillermo Martínez
- Subjects
- *
CHERNETIDAE , *BIOINDICATORS , *NOTHOFAGUS , *FOREST management , *HABITATS - Abstract
Bioindicators could act as early warning indicators of environmental changes, ecosystem stress or taxonomic diversity. Pseudoscorpions have rarely been used as bioindicators, due to lack of information about their ecology, habitat selection, niche preferences and requirements, especially in southern Nothofagus forests. We studied the distribution and abundance of a pseudoscorpion species, Neochelanops michaelseni (Simon 1902), in different vegetation types ( Nothofagus antarctica and N. pumilio forests, grasslands and peatlands) and examined how this species responded to different forest uses (harvesting and silvopastoral management), to explore its utility as a bioindicator. The study was conducted on long-term plots located at two ranches in Tierra del Fuego, using pit-fall traps during one summer. Neochelanops michaelseni abundance was higher in Nothofagus forests than in open ecosystems, which could be attributed to their affinity for litter and coarse woody debris. In N. pumilio forests, the pseudoscorpions were sensitive to harvesting, with similar abundances in harvested forests (aggregated and dispersed retentions) and grasslands. In N. antarctica forests, differences were not detected among unmanaged and silvopastoral managed forests, probably due to higher understory plant growth, and lesser diminishing of litter and debris by thinning than by harvesting. We conclude that the pseudoscorpion, N. michaelseni, can be a good bioindicator for ecosystem conservation and for evaluating recovery rate in the ecological conditions of impacted Nothofagus forests, and that management practice intensities should be regulated to create more suitable habitats for pseudoscorpion diversity conservation. [ABSTRACT FROM AUTHOR]
- Published
- 2015
- Full Text
- View/download PDF
41. A newly described host-symbiont interaction: first record of Dinocheirus panzeri (Pseudoscorpiones: Chernetidae) associated with Cyanistes caeruleus (Aves: Paridae) nests.
- Author
-
Goodenough, Anne E., Mason, Ben, Griggs, Deborah, Stewart, Lindy, Booth, Hannah, and Carpenter, William S.
- Subjects
- *
PSEUDOSCORPIONS , *CHERNETIDAE , *BIRD nests , *AVIAN anatomy - Abstract
The article discusess a new host-symbiont interaction theory by recording Dinocheirus panzeri with Cyanistes caeruleus nests. Topics discussed include global review of pseudoscorpions in bird nests; association of Dinocheirus panzeri with wild birds in Great Britain and avian species; and analysis of suitability of avian nests for pseudoscorpions.
- Published
- 2017
- Full Text
- View/download PDF
42. Allochernes solarii(Pseudoscorpiones: Chernetidae) newly recorded from ant nests in Slovakia
- Author
-
Jana Christophoryová, Martina Červená, Adrián Purkart, and Katarína Krajčovičová
- Subjects
biology ,Central Europe ,Chernetidae ,Holotype ,Zoology ,biology.organism_classification ,ANT ,taxonomy ,Insect Science ,Formica gagates ,lcsh:Zoology ,faunistics ,myrmecophily ,lcsh:QL1-991 ,Ecology, Evolution, Behavior and Systematics - Abstract
Allochernes solarii (Simon, 1898) is recorded for the first time from Slovakia. Six adults and two tritonymphs were found in two nests of Formica gagates Latreille, 1798. A description of the species is provided based on Slovakian specimens and the holotype from Italy.
- Published
- 2018
43. New records of phoretic associations between pseudoscorpions and their hosts in Slovakia (Pseudoscorpiones: Atemnidae, Chernetidae)
- Author
-
Martina Červená, Katarína Krajčovičová, and Jana Christophoryová
- Subjects
Lepidoptera genitalia ,Owlet moth ,biology ,Lamprochernes ,Host (biology) ,Insect Science ,Lonchaeidae ,Chernetidae ,Noctuidae ,Zoology ,biology.organism_classification ,Ecology, Evolution, Behavior and Systematics - Abstract
New cases of phoresy of pseudoscorpions (Pseudoscorpiones: Atemnidae, Chernetidae) are recorded from Slovakia. The phoresy of the species Atemnus politus (Simon, 1878) involving owlet moth (Noctuidae) as a host is documented for the first time not only in Slovakia, but also worldwide. One phoretic female of Lamprochernes chyzeri (Tomosvary, 1883) was attached to the leg of a lance fly (Lonchaeidae). It represents the second known phoresy of the species from Slovakia and the record of a new host.
- Published
- 2021
44. New records of chernetid and cheliferid species (Arachnida: Pseudoscorpiones) from North Macedonia
- Author
-
Dávid Selnekovič, Martina Červená, and Jana Christophoryová
- Subjects
Geography ,Ecology ,biology ,Insect Science ,Cheliferidae ,Chernetidae ,Zoology ,Balkans ,distribution ,faunistics ,new records ,Animal Science and Zoology ,Plant Science ,biology.organism_classification ,Ecology, Evolution, Behavior and Systematics - Abstract
Three pseudoscorpion species from the families Cheliferidae and Chernetidae, Hysterochelifer tuberculatus (Lucas, 1849), Allochernes bulgaricus Hadži, 1939 and Chernes hahnii (C. L. Koch, 1839), are new for the pseudoscorpion fauna of North Macedonia. North Macedonia is the second known country of the distribution of A. bulgaricus in Europe.
- Published
- 2021
45. New data on the Pseudoscorpion fauna of the caves of the Bakony Mountains, Hungary.
- Author
-
NOVÁK, J. and KUTASI, CS.
- Subjects
- *
PSEUDOSCORPIONS , *ARACHNIDA , *CHERNETIDAE , *CARCINOID - Abstract
Examining cave samples from the Bakony Museum of the Hungarian Natural History Museum, Hungary two pseudoscorpion species were found; Chthonius ressli Beier, 1956 and Neobisium carcinoides (Hermann, 1804). C. ressli is new to the pseudoscorpion fauna of Hungary. The morphological characters of the specimens found are discussed in detail and drawings of the C. ressli specimens are given. [ABSTRACT FROM AUTHOR]
- Published
- 2014
46. Haplochernes sp. (Chernetidae) collected from feral raccoon, Procyon lotor in Tokyo
- Author
-
Shin-ichi Hayama, Fumiaki Yamasaki, Takuya Kato, and Kandai Doi
- Subjects
biology ,Phoresis ,Chernetidae ,Zoology ,biology.organism_classification ,Ecology, Evolution, Behavior and Systematics ,Haplochernes - Published
- 2021
47. First record of the genus Lamprochernes (Pseudoscorpiones: Chernetidae) in Albania.
- Author
-
CHRISTOPHORYOVÁ, Jana, GRUĽA, Daniel, and JABLONSKI, Daniel
- Subjects
CHERNETIDAE ,BIOLOGICAL classification - Abstract
The finding of pseudoscorpion Lamprochernes nodosus (Schrank, 1803) represents the first record of the genus Lamprochernes and only the third record of chernetids in Albania. One female was extracted from compost heap near the field at locality Uznovë, Berat County in Albania. A description of the species is provided based on the main morphological and morphometric characters. [ABSTRACT FROM AUTHOR]
- Published
- 2017
48. A new chernetid pseudoscorpion from the Miocene Chiapas - Amber Lagerstätte, Mexico.
- Author
-
Riquelme, Francisco, Piedra-Jiménez, Dulce F., Córdova-Tabares, Víctor, Luna-Castro, Bibiano, and Jin, Jisuo
- Subjects
- *
PSEUDOSCORPIONS , *CHERNETIDAE , *MIOCENE Epoch , *NEOGENE Period , *TERTIARY Period - Abstract
Mayachernes maatiatus, a new genus and species of pseudoscorpion of the family Chernetidae (Arachnida: Pseudoscorpionida), is described from the Miocene Chiapas - Amber Lagerstätte, south of Mexico. This new fossil species represents an adult male specimen with hard-soft tissues preserved in great detail. It differs from all other living chernetids by a combination of diagnostic characters. Anatomical data were collected using high-resolution microscopy with regular to infrared-reflected light. Mayachernes maatiatus is the first newly described fossil species of pseudoscorpion from the Chiapas amber. This taxon also adds to knowledge of the Chernetidae diversity in the southernmost part of North America at the Neogene. [ABSTRACT FROM AUTHOR]
- Published
- 2014
- Full Text
- View/download PDF
49. Phoresy by Americhernes Aff. Incertus (Pseudoscorpiones: Chernetidae) on a Tropical Fly Fannia canicularis (Diptera: Fanniidae) in a Fragment of the Atlantic Forest, Brazil.
- Author
-
Lira, André F. A., Tizo-Pedroso, Everton, and Albuquerque, Cleide M. R.
- Subjects
- *
PHORESY , *PSEUDOSCORPIONS , *CHERNETIDAE , *FANNIA , *DIPTERA , *DISPERSAL of insects - Abstract
Pseudoscorpions employ phoresy for dispersal, in which one animal attaches to another for transportation. This study documents the occurrence and phoresy by Americhernes aff. incertus (Pseudoscorpiones: Chernetidae) on the fly Fannia canicularis (Diptera: Fanniidae) in a fragment of semi-deciduous seasonal Atlantic Forest, in the state of Pernambuco, northeast Brazil. The pseudoscorpions were found attached to the ventral surface of six individual flies. To our knowledge, no previous studies have shown the presence of Americhernes aff. incertus in the northeast Atlantic Forest and its use of flies as a dispersal method. [ABSTRACT FROM AUTHOR]
- Published
- 2014
- Full Text
- View/download PDF
50. Wanted : live Chelifer cancroides
- Author
-
Donovan, B. J. and Read, Samantha
- Published
- 2014
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