Biodiversity Data Journal :
Taxonomy & Inventories
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Corresponding author: Dumas Gálvez (dumas.galvezs@up.ac.pa)
Academic editor: Stuart Longhorn
Received: 20 Dec 2023 | Accepted: 12 Jul 2024 | Published: 31 Jul 2024
© 2024 Daniel Murcia-Moreno, Dumas Gálvez
This is an open access article distributed under the terms of the Creative Commons Attribution License (CC BY 4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Citation:
Murcia-Moreno D, Gálvez D (2024) Preliminary checklist of spiders (Araneae) from Coiba National Park, Panama. Biodiversity Data Journal 12: e117642. https://doi.org/10.3897/BDJ.12.e117642
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Coiba National Park is an offshore region on the Pacific side of Panama, which hosts several endemic species of animals and plants. It was declared a UNESCO World Heritage Site in 2005. Despite the title awarded to the Park, knowledge about basic elements of its biodiversity are still lacking, which are of vital relevance for management and conservation policies. For instance, until now, no study had ever monitored the araneofauna diversity of the Park.
Here, we provide the first checklist of spider species in Coiba National Park, including the main island and several surrounding islands. We sampled during several field trips carried out from August 2021 to August 2023. We identified at least 152 species (98 genera and 30 families) and we report three new spiders species for Panama, namely Ctenus nigrolineatus Berland (1913), Chapoda gitae Zhang & Maddison (2012) and Sarinda nigra Peckham & Peckham (1892). We discuss the implications of our results and recommend future lines of work that include DNA barcoding, monitoring of population and community dynamics, plus linkage of climatic data from the newly-installed meteorological station on the Island.
Araneae, checklist, Coiba, inventory, island
Species diversity, abundance and distribution of biota are universal components of national biodiversity inventories. In conjunction with identifying species, there is also a need to monitor them temporally and spatially. The purpose of monitoring focuses on measuring the condition, status and change of biological diversity to provide information for management actions and achieve conservation outcomes, while improving our fundamental understanding of ecosystems (
One of the useful groups for such inventory studies are the arachnids, where we refer to their total diversity as the arachnofauna. Within these, the spiders (i.e. the araneofauna) are a particularly important subgroup due to their high taxonomic diversity, abundance and their predatory role within terrestrial ecosystems. Spiders often play an important function in both natural and human modified ecosystems, such as controlling pest populations in agriculture or vectors of concern for public health (
Coiba National Park is in the Gulf of Chiriquí (
This study was carried out between August 2021 and August 2023, when a total of 15 field expeditions were conducted, visiting 13 locations in Coiba and nearby islands (Fig.
Location |
Coordinates |
Altitude (m) |
Habitat type |
1. Old main prison |
|
220 |
Anthropogenic |
2. Coiba Scientific Station |
|
50 |
Mixed forest |
3. MiAmbiente Station |
|
70 |
Anthropogenic |
4. Mirador Alto |
|
133 |
Mixed forest |
5. Mirador Gambute |
|
136 |
Mixed forest |
6. Playa Hermosa |
|
20 |
Mixed forest |
7. San Juan |
|
0 |
Coastal beach / Mangrove) |
8. Sendero de Coiba AIP |
|
80 |
Mixed forest |
9. Sendero Los Monos |
|
125 |
Mixed forest |
10. Sendero Santa Cruz |
|
134 |
Mixed forest |
11. Canales Afuera Island |
|
65 |
Mixed forest |
12. Jicaron Island |
|
79 |
Mixed forest |
13. Coibita Island |
|
121 |
Mixed forest |
The samples were preserved in 70% ethanol and are stored in the laboratory of Dr Dumas Gálvez at the Central American Master Program in Entomology at the University of Panama. All samples are available for future study on request. We carried out identifications by means of published guides in scientific articles, books, websites and, in a few instances, by direct communication with specialists of different groups (Suppl. material
A total of 635 individuals were identified belonging to 152 species from 98 genera in 30 families (Table
Checklist of spiders in National Park Coiba. Abbreviation for samples: imm = immature. Abbreviations for Guild: AH = Ambush Hunter, CW = Space Web, GH = Ground Hunters, OH = Other Hunters, OW = Orb Web, SP = Specialist and SW = Sensing Web. Affinities: NEO = neotropical, COS = Cosmopolitan, end = endemic and * = new record. Region summarises only the distribution in the American continent: AR = Argentina, BR = Brazil, CA = Central America, C = Caribbean, CO = Colombia, CR = Costa Rica, EC = Ecuador, GT = Guatemala, MX = Mexico, NA = North America, NI = Nicaragua, PA = Panama, PE = PERU, SA = South America. For the location codes, see Table 1. Distributions are based on World Spider Catalogue (2023). All samples are from understorey level with the exception of few individuals collected in the canopy, depicted as ca with the number next to it indicating the number of individuals sampled.
Species |
Samples |
Guild |
Location |
Affinities |
Distribution |
Region |
Fam. Anyphaenidae |
OH |
|||||
1. Macrophyes elongata Chickering, 1937 |
1 ♂ |
6 |
NEO |
Costa Rica, Panama |
CR-PA |
|
2. Wulfila modestus Chickering, 1937 |
1 ♂ |
8 |
NEO |
Panama (end) |
PA |
|
3. Wulfila sp. 1 |
1 ♀ |
9 |
||||
Fam. Araneidae |
OW |
|||||
4. Acacesia tenella (L. Koch, 1871) |
2 ♂ 2 ♀ |
6, 10 |
NEO |
Mexico to Brazil, French Guiana, Guyana |
MX-SA |
|
5. Allocyclosa bifurca (McCook, 1887) |
1 ♀ |
11 |
NEO |
USA to Panama, Turks & Caicos, Cuba, Hispaniola |
NA-CA-C |
|
6. Cyclosa caroli (Hentz, 1850) |
9 ♀ 1 imm |
2, 6, 8, 9, 12 |
NEO |
USA, Caribbean to Bolivia |
NA-C-SA |
|
7. Eriophora ravilla (C. L. Koch, 1844) |
2 ♀ |
4, 6 |
NEO |
USA to Brazil |
NA-SA |
|
8. Eustala bifida F. O. Pickard-Cambridge, 1904 |
1 ♂ 2 ♀ |
8, 12 |
NEO |
USA to Panama |
NA-CA |
|
9. Eustala aff devia |
5 ♀ |
6, 12 |
||||
10. Eustala exigua Chickering, 1955 |
1 ♂ |
6 |
NEO |
Panama (end) |
PA |
|
11. Eustala fuscovittata (Keyserling, 1864) |
1 ♂ 1 ♀ |
9 |
NEO |
Mexico, Cuba to South America |
MX-C-CA |
|
12. Eustala guttata F. O. Pickard-Cambridge, 1904 |
4 ♂ 5 ♀ |
1, 3, 5, 6, 8, 9, 13 |
NEO |
Mexico to Brazil |
MX-SA |
|
13. Eustala scutigera (O. Pickard-Cambridge, 1898) |
4 ♂ 10 ♀ |
8, 9, 12, 13 |
NEO |
Mexico to Panama |
MX-CA |
|
14. Eustala semifoliata (O. Pickard-Cambridge, 1899) |
2 ♀ 1 imm |
4, 9, 11 |
NEO |
Central America |
CA |
|
15. Eustala sp. 1 |
1 ♂ |
8 |
||||
16. Eustala sp. 2 |
1 ♀ |
7 |
||||
17. Eustala sp. 3 |
58 imm |
3, 4, 6, 7, 8, 9, 10, 12 |
||||
18. Eustala tantula Chickering, 1955 |
1 ♂ |
10 |
NEO |
Panama (end) |
||
19. Larinia directa (Hentz, 1847) |
1 ♀ 2 imm |
7, 9 |
NEO |
USA to Brazil |
NA-SA |
|
20. Metazygia keyserlingi Banks, 1929 |
1 ♂ 4 ♀ |
9, 12 |
NEO |
Costa Rica, Panama, Colombia, Trinidad |
CA-SA |
|
21. Micrathena horrida (Taczanowski, 1873) |
1 ♀ |
12 |
NEO |
Greater Antilles, Mexico to Argentina |
MX-C-SA |
|
22. Parawixia hypocrita (O. Pickard-Cambridge, 1889) |
1 ♀ 9 imm |
6, 8, 9, 12 |
NEO |
Guatemala to Brazil |
CA-SA |
|
23. Parawixia sp. 1 |
1 ♂ |
9 |
||||
24. Pronous intus Levi, 1995 |
1 ♀ 1 imm |
6, 10 |
NEO |
Costa Rica to Brazil |
CA-SA |
|
25. Wagneriana tauricornis (O. Pickard-Cambridge, 1889) |
5 ♂ 19 ♀ 7 imm |
6, 8, 9, 10, 11, 12, 13 |
NEO |
USA to Peru |
NA-SA |
|
26. Witica crassicaudus (Keyserling, 1865) |
2 ♀ 2 imm |
9, 11, 12 |
NEO |
Mexico to Peru |
MX-SA |
|
Fam. Caponiidae |
SP |
|||||
27. Nops largus Chickering, 1967 |
1 ♂ |
8 |
NEO |
Panama (end) |
PA |
|
Fam. Cheiracanthiidae |
OH |
|||||
28. Eutichurus putus O. Pickard-Cambridge, 1898 |
1 ♀ |
4 |
NEO |
Panama, Colombia, Ecuador, Peru, Brazil |
PA-SA |
|
Fam. Clubionidae |
OH |
|||||
29. Elaver cf. tigrina |
1 ♂ 3 ♀ |
6, 9 |
||||
30. Elaver lutescens (Schmidt, 1971) |
1 ♀ |
8 |
NEO |
Panama to Brazil |
PA-SA |
|
31. Elaver sp. 1 |
1 ♀ |
9 |
||||
32. Elaver spp. |
11 imm1ca |
6, 8, 9, 13 |
||||
Fam. Corinnidae |
GH |
|||||
33. Castianeira sp. 1 |
1 ♀ |
9 |
||||
34. Castianeira sp. 2 |
1 ♀ 1 imm |
6, 13 |
||||
35. Corinna bulbosa F. O. Pickard-Cambridge, 1899 |
2 ♂ 1 ♀ |
8, 9 |
NEO |
Mexico to Panama |
MX-CA |
|
36. Corinna sp. 1 |
1 ♀ |
6 |
||||
37. Creugas cf. mucronatus |
1 ♀ |
9 |
||||
38. Mazax spinosa (Simon, 1898) |
1 ♂ 4 ♀ 3 imm |
2, 3, 4, 6, 13 |
NEO |
Guatemala, Panama, St. Lucia, St. Vincent |
CA-C |
|
39. Simonestus sp. 1 |
1 ♀ 1 imm |
9 |
||||
Fam. Ctenidae |
OH |
|||||
40. Acanthoctenus lamarrei Arizala, Labarque & Polotow, 2021 |
5 ♂ 3 ♀ 2 imm |
8 |
NEO |
Panama (end) |
PA |
|
41. Ancylometes bogotensis (Keyserling, 1877) |
1 ♂ 4 ♀ 3 imm |
6, 9 |
NEO |
Honduras to Bolivia |
CA-SA |
|
42. Ctenus nigrolineatus * Berland, 1913 |
1 ♂ 3 ♀ 2 imm |
8, 9, 12 |
NEO |
Ecuador |
PA, EC |
|
43. Kiekie barrocolorado Polotow & Brescovit, 2018 |
1 ♂ |
6 |
NEO |
Panama (end) |
PA |
|
44. Kiekie panamensis Polotow & Brescovit, 2018 |
4 ♂ 2 ♀ 2 imm |
3, 6, 8, 9, 10 |
NEO |
Panama (end) |
PA |
|
45. Phoneutria depilata (Strand, 1909) |
1 ♂ 1 ♀ |
6 |
NEO |
Guatemala, Honduras, Nicaragua, Costa Rica, Panama, Colombia, Ecuador |
CA-SA |
|
46. Genus. 1 sp. 1 |
3 ♂ 2 ♀ 1 imm |
6, 9 |
||||
Fam. Cyrtaucheniidae |
SW |
|||||
47. Bolostromus panamanus (Petrunkevitch, 1925) |
1 ♂ 2 ♀ |
6, 9, 13 |
NEO |
Costa Rica, Panama |
CR-PA |
|
Fam. Filistatidae |
SW |
|||||
48. Labahitha marginata (Kishida, 1936) |
1 ♀ |
13 |
COS |
Taiwan, Philippines, Papua New Guinea, Pacifi Is. Introduced to Mexico, Central America, Brazil |
MX-SA |
|
Fam. Gnaphosidae |
GH |
|||||
49. Zimiromus tropicalis (Banks, 1909) |
1 ♀ |
13 |
NEO |
Costa Rica, Panama |
CR-PA |
|
Fam. Hersiliidae |
SW |
|||||
50. Neotama mexicana (O. Pickard-Cambridge, 1893) |
1 ♀ 1 imm |
7, 9 |
NEO |
USA to Peru, Guyana |
NA-SA |
|
Fam. Lycosidae |
GH |
|||||
51. Allocosa cf. panamena |
4 ♂ 3 ♀ 1 imm |
2, 8, 9 |
||||
52. Arctosa sp. 1 |
1 ♂ |
9 |
||||
53. Hogna sp. 1 |
2 ♂ 1 ♀ |
1, 3 |
||||
Fam. Mimetidae |
SP |
|||||
54. Gelanor zonatus (C. L. Koch, 1845) |
3 ♂ 1 imm |
9 |
NEO |
Mexico to Uruguay |
MX-SA |
|
55. Mimetus trituberculatus O. Pickard-Cambridge, 1899 |
3 ♂ 8 ♀ 2 imm |
3, 6, 8, 9, 13 |
NEO |
Panama (end) |
PA |
|
56. Mimetus verecundus Chickering, 1947 |
1 ♀ |
9 |
NEO |
Panama (end) |
PA |
|
Fam. Nephilidae |
OW |
|||||
57. Trichonephila clavipes (Linnaeus, 1767) |
1 ♂ 1 ♀ |
11 |
NEO |
USA to Argentina. Introduced to São Tomé and Príncipe |
NA-SA |
|
Fam. Oonopidae |
GH |
|||||
58. Costarina cf. recondita |
1 ♀ |
8 |
||||
59. Ponsoonops sp. 1 |
1 ♂ |
8 |
||||
Fam. Oxyopidae |
OH |
|||||
60. Hamataliwa sp. 1 |
1 imm |
9 |
||||
Fam. Pholcidae |
CW |
|||||
61. Modisimus cf. guatuso |
1 ♂ 2 ♀ 2 imm |
6, 8, 9 |
||||
62. Modisimus sp. 1 |
1 imm |
6 |
||||
63. Metagonia delicata (O. Pickard-Cambridge, 1895) |
2 ♂ |
9 |
NEO |
Mexico to Panama |
MX-CA |
|
64. Metagonia sp. 1 |
2 ♀ca |
6 |
||||
65. Physocyclus sp. 1 |
3 ♀ |
3, 13 |
||||
Fam. Salticidae |
OH |
|||||
66. Acragas peckhami (Chickering, 1946) |
3 ♂ 2 ♀ |
6, 7, 9, 11, 13 |
NEO |
Panama, Colombia |
PA-CO |
|
67. Anasaitis canalis (Chamberlin, 1925) |
2 ♂ 5 ♀ |
6, 8, 11 |
NEO |
Panama, Colombia |
PA-CO |
|
68. Chapoda gitae * Zhang & Maddison, 2012 |
1 ♂ |
7 |
NEO |
Colombia, Ecuador |
CO-EC |
|
69. Chapoda recondita (G. W. Peckham & E. G. Peckham, 1896) |
2 ♂ 5 ♀ 1 imm |
9 |
NEO |
Guatemala, Costa Rica, Panama |
GT, CR-PA |
|
70. Cobanus extensus (G. W. Peckham & E. G. Peckham, 1896) |
5 ♀ |
6, 11, 13 |
NEO |
Panama (end) |
PA |
|
71. Colonus sp. 1 |
2 imm |
6, 8 |
||||
72. Corythalia opima (G. W. Peckham & E. G. Peckham, 1885) |
1 ♂ 1 ♀ 1 imm |
8, 9, 13 |
NEO |
USA, Mexico, Guatemala, El Salvador |
NA-CA |
|
73. Corythalia spiralis (F. O. Pickard-Cambridge, 1901) |
2 ♂ |
6, 13 |
NEO |
Colombia, Venezuela, French Guiana, Brazil |
SA |
|
74. Corythalia sulphurea (F. O. Pickard-Cambridge, 1901) |
1 ♀ |
11 |
NEO |
Costa Rica, Panama |
CR-PA |
|
75. Habronattus mexicanus (G. W. Peckham & E. G. Peckham, 1896) |
1 ♀ |
1 |
NEO |
USA to Panama, Caribbean |
NA-C-CA |
|
76. Leptofreya bifurcata (F. O. Pickard-Cambridge, 1901) |
1 ♂ |
13 |
NEO |
Mexico, Panama |
MX, PA |
|
77. Lyssomanes sp. 1 |
5 imm |
3, 6, 8, 9 |
||||
78. Menemerus bivittatus (Dufour, 1831) |
1 ♀ |
13 |
COS |
Africa. Introduced to North, Central and South America, southern Europe, Turkey, India, China, Taiwan, Japan, Australia, Pacific Is. |
NA-CA-SA |
|
79. Myrmapana panamensis (Galiano, 1969) |
1 ♂ 1 imm |
3 |
NEO |
Panama, Argentina |
PA, AR |
|
80. Noegus spiralifer (F. O. Pickard-Cambridge, 1901) |
1 ♂ |
9 |
NEO |
Guatemala, Panama |
GU, PA |
|
81. Psecas sp. 1 |
1 imm |
8 |
||||
82. Sarinda nigra * G. W. Peckham & E. G. Peckham, 1892 |
1 ♂ 2 ♀ 1 imm |
6 |
NEO |
Nicaragua, Guyana, Brazil, Paraguay, Argentina |
NI, SA |
|
83. Sidusa flavens (G. W. Peckham & E. G. Peckham, 1896) |
10 ♂ 1 imm |
4, 5, 7, 8, 9, 11 |
NEO |
Panama (end) |
PA |
|
84. Xanthofreya albosignata (F. O. Pickard-Cambridge, 1901) |
1 ♂ |
9 |
NEO |
Guatemala, Panama, Colombia, Brazil |
GU, PA-SA |
|
85. Xanthofreya arraijanica (Chickering, 1946) |
1 ♂ |
9 |
NEO |
Panama, Colombia |
PA, CO |
|
Fam. Scytodidae |
OH |
|||||
86. Scytodes cf. intricata |
3 ♂ 3 ♀ 7 imm |
1, 3, 8, 9 |
||||
87. Scytodes fusca Walckenaer, 1837 |
2 ♂ 3 ♀ 4 imm |
8, 9, 11, 13 |
NEO |
Northern to Southern America. Introduced to Europe, Africa, Seychelles, India, Myanmar, China, Japan, Hawaii |
NA-SA |
|
88. Scytodes sp. 1 |
1 imm |
6 |
||||
Fam. Selenopidae |
AH |
|||||
89. Selenops sp. 1 |
2 imm |
3, 9 |
||||
90. Selenops sp. 2 |
1 imm |
6 |
||||
Fam. Senoculidae |
OH |
|||||
91. Senoculus rubicundus Chickering, 1953 |
1 ♀ 10 imm |
4, 6, 8, 9, 10, 11 |
NEO |
Panama (end) |
PA |
|
Fam. Sparassidae |
OH |
|||||
92. Meri sp. 1 |
1 imm |
6 |
||||
93. Meri sp. 2 |
3 imm |
9, 11 |
||||
94. Nolavia sp. 1 |
1 ♀ |
3 |
||||
95. Nolavia stylifer (F. O. Pickard-Cambridge, 1900) |
1 ♂ |
6 |
NEO |
Mexico, Brazil |
MX, BR |
|
96. Sparianthis chickeringi (Gertsch, 1941) |
1 ♀ 1 imm |
8, 10 |
NEO |
Panama (end) |
PA |
|
97. Uaiuara sp. 1 |
1 imm |
9 |
||||
Fam. Tetragnathidae |
OW |
|||||
98. Dolichognatha pentagona (Hentz, 1850) |
1 ♂ 1 ♀ 2 imm |
8, 10 |
NEO |
USA to Venezuela |
NA-SA |
|
99. Dolichognatha spinosa (Petrunkevitch, 1939) |
4 ♂ 2 ♀ 5 imm |
6, 9, 12, 13 |
NEO |
Panama (end) |
PA |
|
100. Leucauge saphes Chamberlin & Ivie, 1936 |
1 ♀ 1 imm |
8, 9 |
NEO |
Panama (end) |
PA |
|
101. Leucauge sp. 1 |
1 imm |
11 |
||||
102. Leucauge sp. 2 |
2 ♀ 1 imm |
12 |
||||
103. Metabus cf. debilis |
1 ♂ |
13 |
||||
104. Tetragnatha cambridgei Roewer, 1942 |
1 ♂ |
13 |
NEO |
Mexico, Central America, Puerto Rico |
MX-C-CA |
|
105. Tetragnatha pallida O. Pickard-Cambridge, 1889 |
3 ♂ 11 ♀ 1 imm |
2, 3, 6, 8, 9, 11, 13 |
NEO |
Costa Rica, Panama |
CR, PA |
|
106. Tetragnatha tenuissima O. Pickard-Cambridge, 1889 |
2 ♂ 8 ♀ 1 imm |
6, 9, 11 |
NEO |
Mexico, Central America, Caribbean to Brazil, Argentina |
MX-CA-C-SA |
|
107. Tetragnatha sp. 3 |
7 imm |
3, 6, 9, 11, 12 |
||||
Fam. Theraphosidae |
GH |
|||||
108. Sericopelma sp. 1 |
1 ♀ |
8 |
||||
Fam. Theridiidae |
CW |
|||||
109. Ariamnes attenuatus O. Pickard-Cambridge, 1881 |
1 ♂ 3 ♀ 1 imm |
6, 9, 11 |
NEO |
Costa Rica, Caribbean to Argentina |
CR, C-SA |
|
110. Chrysso albomaculata O. Pickard-Cambridge, 1882 |
1 ♀ |
9 |
NEO |
USA, Mexico to Brazil, Caribbean |
NA-C-SA |
|
111. Chrysso cf. vallensis |
1 ♂ 2 ♀ |
6, 9 |
||||
112. Cryptachaea cf. taeniata |
6 ♀ 2 imm |
6, 8, 10 |
||||
113. Dipoena sp. 1 |
1 ♂ |
11 |
||||
114. Dipoena sp. 2 |
1 ♀ |
8 |
||||
115. Emertonella cf. taczanowskii |
1 ♂ |
6 |
||||
116. Episinus cf. pyrus |
3 imm |
8, 9, 10 |
||||
117. Episinus sp. 1 |
1 ♂ |
11 |
||||
118. Episinus sp. 2 |
2 ♂ 1 ♀ |
9 |
||||
119. Hentziectypus sp. 1 |
1 ♀ |
3 |
||||
120. Neopisinus bruneoviridis (Mello-Leitão, 1948) |
3 ♀ |
6, 9, 13 |
NEO |
Panama, Trinidad to Brazil |
PA, C-BR |
|
121. Neopisinus putus (O. Pickard-Cambridge, 1894) |
9 ♂ 14 ♀10 imm |
3, 4, 6, 8, 9, 10, 13 |
NEO |
Mexico to Panama |
MX-CA |
|
122. Neospintharus sp. 1 |
1 ♂ |
9 |
||||
123. Phycosoma altum (Keyserling, 1886) |
1 ♂ 1 ♀ |
11, 13 |
NEO |
Mexico to Brazil. Introduced to Hawaii |
MX-BR |
|
124. Rhomphaea cf. projiciens |
3 ♀ |
5, 9 |
||||
125. Rhomphaea metaltissima Soares & Camargo, 1948 |
1 ♀ |
4 |
NEO |
Panama to Brazil |
PA-BR |
|
126. Rhomphaea paradoxa (Taczanowski, 1873) |
3 ♂ 2 ♀ 1 imm |
1, 4, 8, 9, 10 |
NEO |
St. Vincent, Mexico to Brazil |
MX-BR, C |
|
127. Theridion sp. 1 |
1 ♀ |
11 |
||||
128. Thwaitesia affinis O. Pickard-Cambridge, 1882 |
2 ♂ 4 ♀ 5 immca |
3, 4, 6, 9, 10 |
NEO |
Panama to Paraguay |
PA-SA |
|
129. Thwaitesia sp. 1 |
2 imm |
9, 11 |
||||
130. Wamba crispulus (Simon, 1895) |
1 ♀ |
13 |
NEO |
Canada to Brazil, Caribbean |
NA-SA, C |
|
Fam. Theridiosomatidae |
OW |
|||||
131. Epilineutes globosus (O. Pickard-Cambridge, 1896) |
3 imm |
9, 11 |
NEO |
Mexico to Brazil |
NA-SA |
|
132. Naatlo sp. 1 |
1 ♂ |
9 |
||||
Fam. Thomisidae |
AH |
|||||
133. Epicadus taczanowskii (Roewer, 1951) |
1 ♂ |
9 |
NEO |
Hispaniola, Costa Rica, Panama to Peru, Bolivia, Brazil |
C, CR-SA |
|
134. Epicadus tuberculatus (Petrunkevitch, 1910) |
1 ♂ 1 ♀ |
8, 11 |
NEO |
Panama, Ecuador, Peru, Brazil |
PA, EC,PE, BR |
|
135. Misumenoides sp. 1 |
1 imm |
5 |
||||
136. Misumenoides sp. 2 |
1 imm |
1 |
||||
137. Synema sp. 1 |
1 imm |
7 |
||||
138. Tmarus ineptus O. Pickard-Cambridge, 1892 |
7 ♀ 5 imm |
5, 6, 7, 9 |
NEO |
Panama, Colombia |
PA, CO |
|
139. Tmarus intentus O. Pickard-Cambridge, 1892 |
1 ♀ |
6 |
NEO |
Guatemala, Panama |
GU, PA |
|
140. Tmarus probus Chickering, 1950 |
1 ♂ |
13 |
NEO |
Panama (end) |
PA |
|
141. Tmarus sp. 1 |
1 ♀ |
8 |
||||
142. Tmarus studiosus O. Pickard-Cambridge, 1892 |
2 ♀ |
2, 8 |
NEO |
Panama (end) |
PA |
|
Fam. Trachelidae |
GH |
|||||
143. Trachelas sp. 1 |
2 ♂ |
4, 9 |
||||
Fam. Trechaleidae |
SP |
|||||
144. Cupiennius cf. granadensis |
2 ♂ 6 ♀ 8 imm |
3, 6, 8, 9 |
||||
145. Cupiennius coccineus F. O. Pickard-Cambridge, 1901 |
1 imm |
3 |
NEO |
Costa Rica to Colombia |
CR-CO |
|
146. Cupiennius sp. 1 |
1 imm |
9 |
||||
147. Trechaela extensa (O. Pickard-Cambridge, 1896) |
1 ♂, 4 imm |
9, 11 |
NEO |
Mexico to Panama |
MX-CA |
|
Fam. Uloboridae |
OW |
|||||
148. Miagrammopes simus Chamberlin & Ivie, 1936 |
3 ♂ 1 ♀ |
8, 9 |
NEO |
Panama (end) |
PA |
|
149. Miagrammopes sp. 1 |
1 ♀ 2 imm |
9 |
||||
150. Philoponella tingens (Chamberlin & Ivie, 1936) |
1 ♂ 3 ♀ 1 imm |
8, 9, 13 |
NEO |
Mexico to Colombia |
MX-SA |
|
151. Uloborus sp. 1 |
1 imm |
2 |
||||
152. Uloborus trilineatus Keyserling, 1883 |
3 ♀ 4 imm |
8, 9, 13 |
NEO |
Mexico to Argentina |
MX-SA |
The spiders collected fell into seven functional groups (i.e. guilds, Table
In terms of biogeography, 150 species are of Neotropical origin, with varying ranges of distribution; for example, we can highlight five species in the range NA-CA, twelve species in NA-SA, five species in CA-SA, nine species in MX-SA, seven species in MX-CA, five species in CR-PA and three species in CO-PA, amongst other regional disitributions. The species Labahitha marginata (Kishida, 1936) and Menemerus bivittatus (Dufour, 1831) have a cosmopolitan distribution (
Panama contains between 1223 (
It is very likely that further work will reveal more species since our rarefaction curve has not yet reached a plateau, which also means that we cannot make meaninful comparisons between islands and sites at this point. Importantly, higher plant diversity, increased complexity of plant architectures and greater prey abundance strongly correlate with higher spider diversity (
Another aspect of utmost importance is the complex interaction of climatic and physical factors, such as high rainfall, humidity and topographic characteristics of Coiba that were not considered during our monitoring. These elements can influence the distribution of the various functional groups within the available microhabitats, because of variation in sites for foraging, shelter or reproduction (
At the biogeographic level, we have identified species with full distribution in the American continent, Central – South America and North – Central America, in line with the idea that the isthmus of Panama has been a point of encounter and exchange for North and South American spider fauna (
It is important to note that, in long-inhabited islands, the presence of human settlements has facilitated the introduction of diverse biota, where it is often unknown whether their arrival occurs naturally or through human intervention (
Regarding endemism, Coiba National Park contains a great diversity of fauna and flora, approximately 70 species are considered endemic, including birds, mammals, plants, insects and arachnids (
In other island studies, in Galapagos,
In conclusion, this study provides a taxonomic baseline and shows that Coiba National Park still offers vast possibilities for revealing its complete arachnofauna, even for the relatively well known araneofauna, i.e. spiders. Understanding biodiversity and species distribution is an essential part of conservation programmes. Obtaining this information is useful for the long-term management and effective use of biological resources across Panama and beyond and is important for monitoring and conservation actions, based on distributional, temporal and spatial changes. Establishing a list of species in insular areas - where periodic and long-term research is logistically difficult - compared to continental areas, will be useful for future goals, such as monitoring or conservation assessment. For example, Coiba National Park offers the opportunity to study ecological and evolutionary processes, by comparing spider populations and communities with those in the mainland. Moreover, it is of great importance to incorporate current tools for the evaluation of the local araneofauna, which includes DNA barcoding, monitoring of population and community dynamics, plus use of the newly-installed meteorological station on the Island. For example, DNA barcoding could reveal cryptic species or help identify species when only the juveniles are available (
We thank Coiba Scientific Station (project code 13) and Sistema Nacional de Investigación for funding this study. We also thank the staff of Museum David G. Fairchild at the University of Panama for access to the arachnological collection. Finaly, we thank Yostin Añino for the support to create the maps and Dr Sabrina Amador who facilitated the use of her laboratory for taking photographs.
Idea conception for study by DG. Fieldwork by DM and DG. Spider identification by DM. Results analysis by DM and DG. Manuscript drafting by DM and DG. Revision of last version by DM and DG.
References used for spider identification and pictures of the new three species reported for Panama.
Summary of species richness and abundance of spiders per site collected in Coiba National Park, from August 2020 to August 2022.