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Inicio Revista Mexicana de Biodiversidad Spiders of the Orbiculariae clade (Araneae: Araneomorphae) from Calakmul municip...
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Vol. 88. Núm. 1.
Páginas 154-162 (marzo 2017)
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Vol. 88. Núm. 1.
Páginas 154-162 (marzo 2017)
Ecology
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Spiders of the Orbiculariae clade (Araneae: Araneomorphae) from Calakmul municipality, Campeche, Mexico
Arañas del clado Orbiculariae (Araneae: Araneomorphae) del municipio Calakmul, Campeche, México
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Daniela T. Candia-Ramíreza,
Autor para correspondencia
, Alejandro Valdez-Mondragóna,b
a Colección Nacional de Arácnidos, Departamento de Zoología, Instituto de Biología, Universidad Nacional Autónoma de México, Apartado postal 70-153, Ciudad Universitaria, Coyoacán, 04510 Ciudad de México, Mexico
b Conacyt Research Fellow, Laboratorio of Aracnología, Laboratorio Regional de Biodiversidad y Cultivo de Tejidos Vegetales del Instituto de Biología, Universidad Nacional Autónoma de México, sede Tlaxcala, Contiguo FES-Zaragoza Campus III, Ex Fábrica San Manuel de Morcom s/n, San Miguel Contla, 90640 Municipio de Santa Cruz Tlaxcala, Tlaxcala, Mexico
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Table 1. Number of genera and species per family of orb-weaver spiders previously deposited in CNAN plus those collected in October 2011.
Table 2. Updated diversity of orb-weaver spiders considering the published records until 2005 and the results from this study.
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Abstract

A study was conducted to determine the biological richness of orb-weaver spiders from Calakmul municipality, Campeche, Mexico. Material deposited in the Colección Nacional de Arácnidos, Instituto de Biología, UNAM was revised. In addition, 16 collecting events were made in 14 localities of Calakmul municipality during this study. The collections were made using beating sheets and manual technique. A total of 1,151 specimens belonging to 8 families, 56 genera and 100 species were reviewed and identified. Two new species and 3 considered possibly new were found, which cannot be confirmed until specimens of both sexes are collected. According to previous studies and this work, 10 families, 65 genera and 119 species of spiders of orb-weaver spiders are present in Calakmul municipality, of which 4 families, 32 genera and 74 species are recorded for the first time. Furthermore, this work adds 3 genera and 10 species to the known diversity for the country, making a total of 14 families, 139 genera and 685 species of orb-weaver spiders recorded for Mexico.

Keywords:
Species richness
Calakmul
Orb-weaver spiders
Yucatán Peninsula
Resumen

Se realizó un estudio con el objetivo de conocer la riqueza biológica de arañas tejedoras de redes orbiculares del municipio de Calakmul, Campeche, México. Se revisó material depositado en la Colección Nacional de Arácnidos, Instituto de Biología, UNAM. Además, se realizaron 16 muestreos en 14 localidades del municipio Calakmul para la recolecta de ejemplares. Las recolectas se realizaron por medio del uso de redes de golpeo y técnica manual. Se recolectaron, revisaron e identificaron 1,151 ejemplares pertenecientes a 8 familias, 56 géneros y 100 especies. Dos especies nuevas y otras 3 se consideran posiblemente nuevas, lo que podrá confirmarse hasta obtener ejemplares de ambos sexos. De acuerdo con estudios previos y este trabajo, en el municipio Calakmul se encuentran presentes 10 familias, 65 géneros y 119 especies de arañas tejedoras, de las cuales 4 familias, 32 géneros y 74 especies se registran por primera vez. Además, este trabajo adiciona 3 géneros y 10 especies a la diversidad conocida para el país, siendo un total de 14 familias, 139 géneros y 685 especies de arañas tejedoras de redes orbiculares registradas para México.

Palabras clave:
Riqueza específica
Calakmul
Arañas tejedoras
Península de Yucatán
Texto completo
Introduction

The Calakmul municipality is the largest in the state of Campeche, in the center of the Yucatán Peninsula, Mexico (Conabio, 1995; Galindo-Leal, 1999; Ibarra-Manríquez, Villaseñor, Durán, & Meave, 2002). According to Galindo-Leal (1999) this region contains the greatest number of species in the Yucatán Peninsula because it is located near 5 mountain ranges, which promote this high biological richness (Villaseñor, Maeda, Colín-López, & Ortiz, 2005). The species community at Calakmul has Neotropical and Nearctic affinities, that is the reason it holds a Biosphere Reserve (Reserva de la Biosfera de Calakmul), bordering the Guatemalan department of El Petén to the south. It occupies 7,231km2 and includes about 12% of the subperennial jungles of Mexico. This reserve is one of the largest protected areas in Mexico, covering more than 14% of the state and it is considered one of the most diverse of Mexico since it conserves many species, some of them threatened (Arreola, Villalobos, Hernández, Sánchez, & Caamal, 2008; Conabio, 1995; Folan and García, 2001).

In Mexico there are reported 2,385 species of spiders, 453 genera, and 69 families (Francke, 2013; World Spider Catalog, 2016), representing 5.1% of the total world diversity (113 families, 4,025 genera, and 46,351 species), and one of the most studied spider groups has been the orb-weaver spiders. Orb-weavers are among the most diverse lineages of araneomorph spiders and are represented by 2 superfamilies: Araneoidea, with 19 families, 1,132 genera, and 12,370 species, and Deinopoidea, with 2 families, 20 genera and 341 species (Hormiga and Griswold, 2014; World Spider Catalog, 2016). According to Jiménez (1996), García-Villafuerte (2009), Ibarra-Núñez, Maya-Morales, and Chamé-Vázquez (2011), and World Spider Catalog (2016), in Mexico there are currently distributed 13 families, 144 genera and 688 species of orb-weaver spiders. In the state of Campeche there are reported 32 genera and 41 species of spiders representing almost one-third of the endemic species of Mexico (Jiménez, 1996); however, there are no studies on diversity of orb-weavers and the few previous records were made by sporadic collections. Hoffmann (1976), Gertsch (1977) and Reddell (1977) reported 6 families, 13 genera and 17 species for Campeche. After that, Exline and Levi (1962), Levi (1957, 1968, 1975, 1976, 1991, 1992, 1995a,b, 1997, 1999, 2005), and Piel (2001) found new records for 23 species of 13 genera of family Araneidae, and 3 species of 3 genera of Theridiidae. Consistent with this information, until 2005, there were reported 6 families, 31 genera and 44 species of orb-weaver spiders from Campeche, being Araneidae and Theridiidae the families with the highest diversity with 16 genera and 27 species, and 11 genera and 13 species respectively. The present study is an update of the diversity of orb-weaver spiders for the last 10 years for Calakmul and Campeche, as well for the Yucatán Peninsula and Mexico.

Materials and methods

We studied unidentified preserved spiders in 80% ethanol from the arachnological collection (CNAN) of Instituto de Biología, UNAM. These specimens were collected in November 1991, June 1997, April and July 1998, July 2001, July 2007, and July 2010 at Calakmul, Campeche. Also we made a survey in October 2011 to collect specimens of orb-weaver spiders.

The sampling was conducted in the rainy season because this is when an increase in the abundance and richness of spiders has been reported in other studies in Mexico (Rodríguez-Rodríguez, Solís-Catalán, & Valdez-Mondragón, 2015; Valdez-Mondragón, 2006). Also, the reproduction of most of the species occurs in this season, being a period where the presence of food is constant (Nogueira, Pinto da Rocha, & Brescovit, 2006). We visited the borders of the Calakmul Biosphere Reserve on the center and south of the municipality (Fig. 1), from October 10 to 17 in 2011 to collect orb-weaver spiders. We visited 14 localities and made 16 samplings (Fig. 1), 14 were diurnal and 2 nocturnal. The criteria for selection of localities were the presence of a high conservation level and low or absent flooding to ease access to the vegetation. The predominant vegetation in the localities was tropical rainforest, vegetation type present in 12 of 14 localities, the other 2 localities presented deciduous forest vegetation and a cave environment. Five localities were well preserved and 9 showed some degree of disturbance, mainly in the southwest portion of the municipality, where there were plots and pastures, instead of forest (Fig. 2). During mornings, we used beating sheets of 70cm×70cm size to collect spiders. We placed them under the trees and shrubs in 1m2 quadrats, and then beat the vegetation with a 40cm long stick. The spiders were collected with arachnological aspirators into plastic vials. At most localities we made about 20 beatings; however, in localities with disturbed vegetation we made only 10. Additionally, we searched under rocks and fallen logs exhaustively for spiders and collected them by hand or using forceps, arachnological aspirators and/or small brushes. At night we searched for orb-weaver spiders on the vegetation using headlamps with white light and collected them with an aspirator or directly into vials. A team of 5 people worked 1h during the day and 2h at night at each locality. Considering that only in 2 localities we made nocturnal collections, the sampling effort was 18h/person, totaling 90h among the 5 participants. All specimens were preserved in glass jars with ethanol (80%), labeled with their respective collection data, and deposited in the CNAN.

Figure 1.

Map of Calakmul municipality showing the 14 localities sampled in October 2011, indicating the type of vegetation of each one.

(0.47MB).
Figure 2.

Differences between localities where the spiders were collected: with a high conservation level (left), and with perturbation (right).

(0.29MB).

The revision of specimens was made in a stereoscopic microscope Nikon SMZ 745T, where sexual and somatic characters were revised for each specimen. The dissection of male pedipalps and epigyna was made following Levi's protocol (1965), and for identifications to species level we used specialized literature and taxonomic keys.

Results

Considering the material previously collected plus the newly collected material in October, we identified 1,151 specimens, belonging to 8 families, 56 genera and 100 species of orb-weaver spiders (Table 1). Regarding the material deposited in the CNAN, we sorted and identified 8 families, 30 genera, and 46 species of orb-weavers (Table 1). The families with the highest number of species were Araneidae with 36 species (78%), and Uloboridae, with 4 species (8.7%). It is important to emphasize that these spiders were captured using mainly manual techniques, and the collections were focused on collecting all arachnid orders. Then, in the sampling made in October 2011 we found a total of 8 families, 50 genera, and 83 species (Table 1). The families with the highest diversity in these samplings were Araneidae and Theridiidae with 35 (42.2%) and 25 (30.1%) species, respectively (Table 1). Considering the published records until 2005 and the new results from this study, in the Calakmul municipality and the state of Campeche, currently 10 families, 65 genera and 119 species of spiders of orb-weaver spiders are reported (Table 2; Appendix 1). The most diverse families were Araneidae with 57 (47.9%) and Theridiidae with 35 species (28.6%) (Table 2).

Table 1.

Number of genera and species per family of orb-weaver spiders previously deposited in CNAN plus those collected in October 2011.

Family  Deposited in CNANCollected at October 2011Total species 
  No. genera  No. species  No. genera  No. species   
Araneidae  20  36  19  35  50 
Theridiidae  16  25  26 
Uloboridae 
Tetragnathidae 
Theridiosomatidae 
Linyphiidae 
Deinopidae 
Nephilidae 
Total  30  46  50  83  100 
Table 2.

Updated diversity of orb-weaver spiders considering the published records until 2005 and the results from this study.

Family  Previously reportedNew recordsTotal species 
  No. genera  No. species  No. genera  No. species   
Araneidae  16  27  24  50  57 
Theridiidae  11  13  16  26  34 
Uloboridae 
Tetragnathidae 
Theridiosomatidae 
Linyphiidae 
Deinopidae 
Nephilidae 
Mysmenidae 
Nesticidae 
Total  32  45  56  100  119 

Two new species were found: Dipoena sp. nov. (Theridiidae) and Hingstepeira sp. nov. (Araneidae), and 4 are considered possibly new: Pozonia sp. (Araneidae), Ceratinopsis sp. (Linyphiidae), Conifaber sp. (Uloboridae), and Ogulnius sp. (Theridiosomatidae). However, in these cases it is necessary to collect adult specimens of both sexes to confirm the identifications, because there are genera with a great number of species that are described from only 1 sex, and proper comparisons with the specimens collected cannot be completed.

Discussion

Regarding the genera of orb-weavers found in this study, the most diverse genera of Araneidae were Mangora Cambridge, 1889 and Micrathena Sundevall, 1833 with 6 species each, whereas 16 genera (61.1%) were represented by a single species (Appendix 1). Among Theridiidae, the most diverse genera were Faiditus Keyserling, 1884 and Theridion Walckenaer, 1805 with 4 species each, whereas 11 genera (42.3%) were represented by 1 species (Appendix 1). The high diversity of Araneidae and Theridiidae has been also reported by Silva and Coddington (1996). According to Deza and Andía (2009), the diversity of Araneidae should increase with manual exhaustive sampling, in both diurnal and nocturnal searches, because it considers every habitat in the field. In this study, one of the collection techniques was manual, but we could only carry out 2 nocturnal collections because of the rain. Therefore, it is possible that the diversity of Araneidae in Calakmul could be higher if more nocturnal collections are made. For Uloboridae, the most diverse genus was Uloborus Latreille, 1806, represented by 3 species, whereas 37.5% of the genera were represented by a single species (Appendix 1). Our results are similar to that found by Silva and Coddington, 1996, in which Uloboridae represented 8.9% of the diversity of orb-weavers collected during rainy season in October in Pakitza, Peru. In the case of Tetragnathidae family, the genus Tetragnatha Latreille, 1804 was the most diverse with 4 species; and Opas Cambridge, 1896 was the only genus represented by a single species (Appendix 1). The diversity of Tetragnathidae was quite similar to that found by Rico, Beltrán, Álvarez, and Flórez (2005) in Gorgona Island, Colombia in which the family represented 8.3% of the diversity of orb-weaver spiders. That study was comparable to ours because they made only one collection event and the altitude, vegetation, and season conditions were similar. For Theridiosomatidae, the most diverse genera were Epeirotypus Cambridge, 1894 and Theridiosoma Cambridge, 1879 with 2 species each one, whereas the genus Ogulnius Cambridge, 1882 was represented by 1 species, which is possibly new (Appendix 1) and the family represents 6% of the total diversity found. According to Silva and Coddington, 1996, the diversity of this family increases at the beginning of the dry season; and the spiders of genus Epeirotypus were collected in spiny trunks of palms, and spiders of genus Theridiosoma were found in webs built over topsoil. Thus, it is important to search for these spiders in different microhabitats, in different types of vegetation, and in different seasons to get a greater species richness.

All the genera found of the families Linyphiidae, Deinopidae, Mysmenidae, Nephilidae, and Nesticidae were represented by 1 species each. According to these results, 65.2% of the genera reported for Calakmul and Campeche are represented by only 1 species (Appendix 1). The low diversity found in some families of orb-weaver spiders has been also reported in other studies. In the study conducted by Rico et al. (2005), the diversity of Uloboridae was greater and represented 13.8% of orb-weavers. In contrast, Ferreira-Ojeda, Flórez, and Sabogal-González (2009) found that family Uloboridae was only represented by 1 species (2.8%) in Sierra Nevada, Santa Marta, Colombia. The difference in results could be influenced by weather, vegetation, and altitude of the localities sampled. The family Linyphiidae presented low diversity, with only 3 genera and 3 species (3.6%). This low diversity is similar to that found by Silva and Coddington (1996), where Linyphiidae represented 1.7% of orb-weaver diversity. That study, as this one, was conducted in tropical rainforest at a low elevation (356m). According to Russell-Smith and Stork (1994), Sørensen (2004) and Ibarra-Núñez et al. (2011) this family is not diverse in low tropical regions and the species richness increases with elevation. In the Yucatán Peninsula, the elevation in the southern region is slightly above 200m, therefore this region is quite low. In contrast, in a revision by Ibarra-Núñez et al. (2011), who studied the diversity of spiders in the Biosphere Reserve of Tacaná Volcano, Chiapas, at an altitude above 2,000m, found that Linyphiidae were represented by 20 species, almost 25% of the diversity of orb-weaver spiders.

The less diverse families in Calakmul were Nephilidae and Deinopidae. The family Nephilidae is not diverse in America, and is represented by only 2 genera and 6 species (World Spider Catalog, 2016). Currently, the genus Nephila has colonized at least 40 islands and landmasses, and many species have an extended distribution (Kuntner and Agnarsson, 2011). In the case of Nephila clavipes (Linnaeus, 1767), it is distributed from the USA to Argentina. The low diversity of the genus could be due to its high dispersion capacity, which limits its diversification and maintains gene flow among geographically distant populations (Kuntner and Agnarsson, 2011). The diversity of Deinopidae is quite similar to Nephilidae; this family is represented by 1 genus and 19 species in America, of which 1 genus and 2 species (Deinopis aurita Cambridge, 1902 and Deinopis longipes Cambridge, 1902) have been reported for Mexico, being D. longipes the species found in this study. In other studies of diversity of orb-weaver spiders, specimens of this family have not been reported (Ferreira-Ojeda et al., 2009; Rico et al., 2005; Romo and Flórez, 2008) or when they are found, are represented by only 1 species (Blanco-Vargas, Amat-García, & Flórez-Daza, 2003; Silva and Coddington, 1996). According to Coddington, Kuntner, and Opell (2012), despite the tropical distribution of the family, their size, and their habits, specimens of this family are poorly represented both in field and in biological collections, therefore they are considered rare.

Of the 8 families, 57 genera, and 100 species of orb-weavers found in this study, only 4 families, 24 genera and 27 species (27%) were previously reported in others works for Calakmul and Campeche. In contrast, 10 genera and 27 species of Araneidae, 9 genera and 20 species of Theridiidae and 15 genera and 27 species of Deinopidae, Linyphiidae, Nephilidae, Tetragnathidae, Theridiosomatidae, and Uloboridae represent new distribution records for Calakmul and Campeche. Regarding the new records for Mexico, 3 genera and 5 species have not previously reported for the country. For Araneidae, the species Ocrepeira serrallesi (Bryant, 1947) was previously reported only from the West Indies (Levi, 1993); and this is the first time that the genus Higstepeira Levi, 1995 is reported for North America (Levi, 1995b). For Theridiidae, Faiditus chickeringi (Exline and Levi, 1962) and Theridion chiriquiLevi, 1959 were previously only reported for Panama (Exline and Levi, 1962; Levi, 1959). In the case of Theridiosomatidae, the genus Ogulnius is reported for North America for the first time (Coddington, 1986). Also, Epeirotypus chavarriaCoddington, 1986 was only previously reported for Costa Rica (Coddignton, 1986), and Theridiosoma zygops (Chamberlin and Ivie, 1936) was reported for Panama (Chamberlin and Ivie, 1936). For Uloboridae, is the first time that the genus Conifaber Opell, 1982 is reported for North America (Grismado, 2004; Lubin, Opell, Eberhard, & Levi, 1982).

Most of the new records for Mexico are for species that were previously registered in localities that are very distant from Calakmul and Campeche, such as Hingstepeira, Conifaber, and Ogulnius. The orb-weaver spiders have a dispersion method called “ballooning” and it consists in the production of silk threads caused by friction of air with the spinnerets. The silk threads act like a parachute, allowing spiders travel long distances (Sutter, 1992). Considering this, it is possible that many species previously registered only for Central and South America, are also distributed in North America, and therefore in Mexico. Regarding the 2 new species Dipoena sp. nov. (Theridiidae) and Hingstepeira sp. nov. (Araneidae), and the possibly new: Pozonia sp. (Araneidae), Ceratinopsis sp. (Linyphiidae), Conifaber sp. (Uloboridae), and Ogulnius sp. (Theridiosomatidae), it is necessary to collect adult specimens of both sexes to confirm the identifications, because there are genera with a great number of species that are described from only 1 sex, and proper comparisons with the specimens collected cannot be carried out.

With the diversity of orb-weavers registered until 2011, in Calakmul and Campeche currently there are found 10 families, 65 genera, and 119 species. However, this diversity could increase if more systematized sampling events and collecting techniques are implemented, and even studying the fluctuation of species numbers could be determined according to the different seasons. Some species that were previously reported for Campeche were not found in this study; the absence of these species in our collections could be influenced by differences in collection techniques and seasonality, but also by degree of perturbation of the native vegetation. In addition, some species such as Hingstepeira sp. nov. are reported from localities inside of the Calakmul Biosphere Reserve and were not found in the present study. Thus, it is possible that this species is endemic to the Reserve, or that it is easily found there because of the high level of conservation, as opposed to some of our other sampling localities (Fig. 2); and the same could be happening with other species. The family Araneidae resulted the most diverse, with 47.9% of the species of orb-weaver spiders, but despite the great number of studies on the taxonomy and species richness of Araneidae, it is considered that almost the 50% of the diversity of the family is still unknown (Coddington and Levi, 1991). Therefore, it is necessary to intensify the number of studies on orb-weaver spiders, mainly in the Neotropical region in order to increase their known diversity, because in these regions is where the greatest level of species richness of this family has been found (Flórez, 1998). According to the diversity of the orb-weavers for Mexico, the families Theridiosomatidae, Mysmenidae, Anapidae, and Symphytognathidae are the less diverse (except Nephilidae and Deinopidae); it is possible that their low diversity is because these spiders are tiny and they are difficult to collect using manual techniques. Therefore, it is recommended that in future collections special techniques should be used to capture these types of spiders, such as collection of leaf litter and the use of Berlese funnels to have a more accurate approach to document the real diversity of these families.

Acknowledgements

We thank Oscar F. Francke for his comments, fieldwork, support and corrections on the manuscript, Juan J. Morrone for his recommendations to improve the manuscript, Griselda Montiel Parra and Diego Barrales Alcalá for their help with the fieldwork, to Guillermo Ibarra for his help with the identification of the spiders, and the reviewers for their comments and improvement of the manuscript. To the Instituto de Biología (IBUNAM) and Posgrado en Ciencias Biológicas of UNAM. The second author thanks to the program “Cátedras Conacyt”, Consejo Nacional de Ciencia y Tecnología (Conacyt) for the scientific support for project No. 59: “Laboratorio Regional de Biodiversidad y Cultivo de Tejidos Vegetales (LBCTV) del Instituto de Biología (IBUNAM), sede Tlaxcala”. To the people from different localities in Campeche for the help and facilities in the fieldwork. The specimens were collected under Scientific Collector Permit FAUT-0175 from the Secretaría de Medio Ambiente y Recursos Naturales (Semarnat) to Oscar F. Francke.

Appendix 1
List of species of orb-weavers registered for Calakmul, Campeche, and Mexico. New records: *=families, genera and species first reported for Calakmul and Campeche, **=genera and species first reported for Mexico.

Families, genera and species  References 
Araneidae
Acacesia   
A. hamata (Hentz, 1847)  Levi, 1976 
Acanthepeira   
A. stellata (Walckenaer, 1805)  Levi, 1976 
Aculepeira 
A. travassosi (Soares and Camargo, 1948)*   
Allocyclosa   
A. bifurca (McCook, 1887)  Levi, 1999 
Araneus
A. expletus (Cambridge, 1889)*   
A. lineatipes (Cambridge, 1889)  Levi, 1991 
A. pegnia (Walckenaer, 1841)  Levi, 1991 
Argiope
A. argentata (Fabricius, 1775)  Levi, 1968 
A. aurantia Lucas, 1833*   
A. blanda Cambridge, 1898  Levi, 1968 
A. submaronica Strand, 1916*   
Carepalxis*
Carepalxis sp.*   
Cyclosa
C. berlandiLevi, 1999 
C. caroli (Hentz, 1850)  Levi, 1999 
C. walckenaeri (Cambridge, 1889)  Levi, 1999 
Eriophora
E. edax (Blackwall, 1863)  Hoffmann, 1976 
E. fuliginea (C. L. Koch, 1838)   
E. ravilla (C. L. Koch, 1844)  Hoffmann, 1976 
E. illicita (Cambridge, 1889)*   
E. scutigera (Cambridge, 1898)*   
Eustala*
E. devia (Gertsch and Mulaik, 1936)*   
E. fuscovittata (Keyserling, 1864)*   
E. guttata F. Cambridge, 1904*   
Gasteracantha*
G. cancriformis (Linnaeus, 1758)*   
Hingstepeira*, **   
Hingstepeira sp. nov.   
Kaira*
K. altiventer Cambridge, 1889*   
Larinia
L. directa (Hentz, 1847)  Levi, 1975 
L. famulatoria (Keyserling, 1883)*   
Mangora
M. calcarifera F. Cambridge, 1904  Levi, 2005 
M. campecheLevi, 2005  Levi, 2005 
M. chicannaLevi, 2005  Levi, 2005 
M. itzaLevi, 2005  Levi, 2005 
M. melanocephala (Taczanowski, 1874)*   
M. mobilis (Cambridge, 1889)  Levi, 2005 
M. passiva (Cambridge, 1889)  Levi, 2005 
M. picta (Cambridge, 1889)*   
Mecynogea
M. lemniscata (Walckenaer, 1841)  Levi, 1997 
Metazygia
M. chicanna Levi, 1995  Levi, 1995 
M. nigrocinta (F. Cambridge, 1904)*   
M. zilloides (Banks, 1898)  Levi, 1995 
Metepeira
M. celestunPiel, 2001 
M. mayaPiel, 2001 
M. minima Gertsch, 1936  Piel, 2001 
M. ventura Chamberlin and Ivie, 1942  Piel, 2001 
Micrathena
M. funebris (Marx, 1898)*   
M. gracilis (Walckenaer, 1841)*   
M. mitrata (Hentz, 1850)*   
M. sagittata (Walckenaer, 1841)  Hoffmann, 1976 
M. sexpinosa (Hahn, 1822)*   
M. triserrata F. Cambridge, 1904*   
Neoscona
N. oaxacensis (Keyserling, 1864)  Hoffmann, 1976 
Ocrepeira*
O. serrallesi (Bryant, 1947)*, **   
Parawixia
P. tredecimnotata F. Cambridge, 1904  Levi, 1992 
Pozonia*
Pozonia sp.*   
Scoloderus
S. cordatus (Taczanowski, 1879)  Levi, 1976 
Verrucosa*
V. arenata (Walckenaer, 1841)*   
Wagneriana*
W. tauricornis (Cambridge, 1889)*   
Deinopidae*
Deinopis 
D. longipes F. Cambridge, 1902*   
Linyphiidae
Ceratinopsis 
Ceratinopsis sp. nov.   
Eperigone
Eperigone sp.  Gertsch, 1977 
Frontinella*
F. potosia Gertsch and Davis, 1946*   
Novafrontina*
N. uncata (F. Cambridge, 1902)*   
Mysmenidae
Maymena   
M. mayana (Chamberlin and Ivie, 1938)  Gertsch, 1977; Reddell, 1977 
Nephilidae*
Nephila 
N. clavipes (Linnaeus, 1767)*   
Nesticidae
Eidmanella   
E. pallida (Emerton, 1875)  Hoffmann, 1976; Reddell, 1977 
Tetragnathidae
Leucauge 
L. argyra (Walckenaer, 1841)*   
L. venusta (Walckenaer, 1841)*   
Opas*
O. lugens Cambridge, 1896*   
Tetragnatha*
T. guatemalensis Cambridge, 1889*   
Tetragnatha sp. 01*   
Tetragnatha sp. 02*   
Tetragnatha sp. 03*   
Theridiidae
Anelosimus 
A. chickeringiLevi, 1965 
A. jucundus (Cambridge, 1896)*   
A. studiosus (Hentz, 1850)*   
Argyrodes
A. elevatus Taczanowski, 1873  Exline and Levi, 1962 
Chrosiothes
C. tonala (Levi, 1954)  Hoffmann, 1976 
Chrysso
C. albomaculata Cambridge, 1882  Hoffmann, 1976; Levi, 1957 
Dipoena*
Dipoena sp.*   
Dipoena sp. nov.   
Episinus*
E. chiapensis Levi, 1955*   
Euryopis
E. spinigera Cambridge, 1895  Hoffmann, 1976 
Faiditus
F. americanus (Taczanowski, 1984)*   
F. caudatus (Taczanowski, 1984)*   
F. chickeringi (Exline and Levi, 1962)*   
F. globosus (Keyserling, 1884)  Exline and Levi, 1962 
Hentziectypus*
H. florens (Cambridge, 1896)*   
Latrodectus
L. geometricus C. L. Koch, 1841  Hoffmann, 1976 
L. mactans (Fabricius, 1775)  Hoffmann, 1976 
Neopisinus*
N. cognatus (Exline and Levi, 1962)*   
Neospintharus*
N. concisus (Lucas, 1846)*   
Nesticodes
N. rufipes (Exline and Levi, 1962Reddell, 1977 
Parasteatoda*
P. tesselata (Keyserling, 1884)*   
Steatoda
S. erigoniformis (Cambridge, 1872)  Hoffmann, 1976 
S. trasversa (Banks, 1898)*   
Stemmops*
Stemmops sp.*   
Theridion
T. chiriquiLevi, 1959* **   
T. hispidum Cambridge, 1898  Reddell, 1977 
T. niveum Cambridge, 1898*   
T. positivum Chamberlin, 1924*   
Thymoites
T. illudens (Gertsch and Mulaik, 1936)  Hoffmann, 1976 
T. luculentus (Simon, 1894)  Hoffmann, 1976 
T. marxi (Crosby, 1906)*   
Tidarren*
T. haemorrhoidale (Bertkau, 1880)*   
T. sisyphoides (Walckenaer, 1841)*   
Wamba
W. crispulus (Simon, 1895)  Hoffmann, 1976 
Theridiosomatidae*
Epeirotypus*   
E. chavarria Coddington, 1896*   
Epeirotypus sp.*   
Ogulnius* **
Ogulnius sp. 01* **   
Theridiosoma*
T. zygops (Chamberlin and Ivie, 1936)* **   
Theridiosoma sp.*   
Uloboridae
Ariston*   
A. albicans Cambridge, 1896*   
Conifaber* **   
Conifaber sp. nov.   
Miagrammopes*
Miagrammopes sp.*   
Philoponella
P. semiplumosa (Simon, 1893)*   
P. signatella (Roewer, 1951)  Hoffmann, 1976 
Uloborus*
U. campestratus Simon, 1893*   
U. segregatus Gertsch, 1936*   
U. trilineatus Keyserling, 1883*   

References
[Arreola et al., 2008]
A. Arreola, G. Villalobos, L. Hernández, C. Sánchez, L. Caamal.
Ordenamiento territorial del Municipio de Calakmul, Campeche: Un estudio enfocado a las funciones del paisaje.
Conanp, (2008),
[Blanco-Vargas et al., 2003]
E. Blanco-Vargas, G.D. Amat-García, E. Flórez-Daza.
Araneofauna orbitelar (Araneae: Orbiculariae) de los Andes de Colombia: comunidades en hábitats bajo regeneración.
Revista Ibérica de Aracnología, 7 (2003), pp. 189-203
[Chamberlin and Ivie, 1936]
R.V. Chamberlin, W. Ivie.
New spiders from Mexico and Panama.
Bulletin of the University of Utah, 27 (1936), pp. 1-103
[Coddington, 1986]
J.A. Coddington.
The genera of the spider family Theridiosomatidae.
Smithsonian Contributions to Zoology, 422 (1986), pp. 1-96
[Coddington et al., 2012]
J.A. Coddington, M. Kuntner, B.D. Opell.
Systematics of the spider family Deinopidae with a revision of the genus Menneus.
Smithsonian Contributions to Zoology, 636 (2012), pp. 1-61
[Coddington and Levi, 1991]
J.A. Coddington, H.W. Levi.
Systematics and evolution of spiders.
Annual Review of Ecology and Systematics, 22 (1991), pp. 565-592
[Conabio, 1995]
Conabio (Comisión Nacional para el Uso y el Aprovechamiento de la Biodiversidad).
Atlas de Reservas de la Biosfera y otras áreas naturales protegidas.
Instituto Nacional de Ecología, Semarnap, (1995),
[Deza and Andía, 2009]
M. Deza, J.M. Andía.
Diversidad y riquezas de especies de la familia Araneidae (Arachnidae, Araneae) en Cicra (Madre de Dios, Perú).
Ecología Aplicada, 8 (2009), pp. 81-91
[Exline and Levi, 1962]
H. Exline, H.W. Levi.
American spiders of the genus Argyrodes (Araneae, Theridiidae).
Bulletin of the Museum of Comparative Zoology, 127 (1962), pp. 75-204
[Ferreira-Ojeda et al., 2009]
L. Ferreira-Ojeda, E. Flórez, A. Sabogal-González.
Arañas orbitelares de un bosque húmedo subtropical de la Sierra Nevada de Santa Marta (Magdalena, Colombia).
Caldasia, 31 (2009), pp. 381-391
[Flórez, 1998]
E. Flórez.
Estructura de comunidades de arañas (Araneae) en el departamento del Valle, Suroccidente de Colombia.
Caldasia, 20 (1998), pp. 173-192
[Folan and García, 2001]
W.J. Folan, J.M. García.
Reserva de la Biosfera Calakmul: los primeros esfuerzos.
XIV Simposio de Investigaciones Arqueológicas en Guatemala. Guatemala, 2000, pp. 383-389
[Francke, 2013]
O.F. Francke.
Biodiversidad de Arthropoda (Chelicerata: Arachnida ex. Acari) en México.
Revista Mexicana de Biodiversidad, 85(Suppl.) (2013), pp. S408-S418
[Galindo-Leal, 1999]
C. Galindo-Leal.
La gran región de Calakmul: prioridades biológicas de conservación y propuesta de modificación de la Reserva de la Biosfera.
Wildlife Fund-México, (1999),
[García-Villafuerte, 2009]
M.A. García-Villafuerte.
La araneofauna (Araneae) reciente y fósil de Chiapas, México.
Revista Mexicana de Biodiversidad, 80 (2009), pp. 633-646
[Gertsch, 1977]
W.J. Gertsch.
Report of cavernicole and epigean spiders from the Yucatán Peninsula.
Association for Mexican Cave Studies Bulletin, 6 (1977), pp. 103-131
[Grismado, 2004]
C.J. Grismado.
Two new species of the spider genus Conifaber Opell 1982 from Argentina and Paraguay, with notes on their relationships (Araneae, Uloboridae).
Revista Ibérica de Aracnología, 9 (2004), pp. 291-306
[Hoffmann, 1976]
A. Hoffmann.
Relación bibliográfica preliminar de las arañas de México (Arachnidae: Araneae).
Instituto de Biología, Universidad Nacional Autónoma de México, (1976),
[Hormiga and Griswold, 2014]
G. Hormiga, C.G. Griswold.
Systematics, phylogeny, and evolution of orb-weaving spiders.
Annual Review of Entomology, 59 (2014), pp. 487-512
[Ibarra-Manríquez et al., 2002]
G. Ibarra-Manríquez, J.L. Villaseñor, R. Durán, J. Meave.
Biogeographical analysis of the flora of the Yucatán Peninsula.
Journal of Biogeography, 29 (2002), pp. 17-30
[Ibarra-Núñez et al., 2011]
G. Ibarra-Núñez, J. Maya-Morales, D. Chamé-Vázquez.
Las arañas del bosque mesófilo de montaña de la Reserva de la Biósfera Volcán Tacaná, Chiapas, México.
Revista Mexicana de Biodiversidad, 82 (2011), pp. 1183-1193
[Jiménez, 1996]
M.L. Jiménez.
Araneae.
pp. 83-101
[Kuntner and Agnarsson, 2011]
M. Kuntner, I. Agnarsson.
Phylogeography of a successful aerial disperser: The golden orb spider Nephila on Indian Ocean Islands.
Biomedical Central Evolutionary Biology, 11 (2011), pp. 119
[Levi, 1957]
H.W. Levi.
The spider genera Chrysso and Tidarren in America.
Journal of the New York Entomological Society, 63 (1957), pp. 59-81
[Levi, 1959]
H.W. Levi.
The spider genera Achaearanea, Theridion, and Spyrothinus from Mexico, Central America and the West Indies (Aranea, Theridiidae).
Bulletin of the Museum of Comparative Zoology, 121 (1959), pp. 57-163
[Levi, 1965]
H.W. Levi.
Techniques for the study of spider genitalia.
Psyche, 72 (1965), pp. 152-158
[Levi, 1968]
H.W. Levi.
The spider genera Gea and Argiope in America (Araneae: Araneidae).
Bulletin of the Museum of Comparative Zoology, 136 (1968), pp. 319-352
[Levi, 1975]
H.W. Levi.
The American orb weaver genera Larinia, Cercidia and Mangora north of Mexico (Araneae, Araneidae).
Bulletin of the Museum of Comparative Zoology, 147 (1975), pp. 101-135
[Levi, 1976]
H.W. Levi.
The orb weaver genera Verrucosa, Acanthepeira, Wagneriana, Acacesia, Wixia, Scoloderus, and Alpaida north of Mexico.
Bulletin of the Museum of Comparative Zoology, 147 (1976), pp. 351-391
[Levi, 1991]
H.W. Levi.
The Neotropical and Mexican species of the orbweaver genera Araneus, Dubiepeira, and Aculepeira (Araneae: Araneidae).
Bulletin of the Museum of Comparative Zoology, 152 (1991), pp. 167-315
[Levi, 1992]
H.W. Levi.
Spiders of the orb weaver genus Parawixia in America (Araneae: Araneidae).
Bulletin of the Museum of Comparative Zoology, 153 (1992), pp. 1-46
[Levi, 1993]
H.W. Levi.
The neotropical orb-weaving spiders of the genera Wixia, Pozonia, and Ocrepeira (Araneae: Araneidae).
Bulletin of the Museum of Comparative Zoology at Harvard College, 153 (1993), pp. 47-141
[Levi, 1995a]
H.W. Levi.
The Neotropical orb-weaver genus Metazygia (Araneae: Araneidae).
Bulletin of the Museum of Comparative Zoology, 154 (1995), pp. 63-151
[Levi, 1995b]
H.W. Levi.
Orb-weaving spiders Actinosoma, Spilasma, Micrepeira, Pronous, and four new genera (Araneae: Araneidae).
Bulletin of the Museum of Comparative Zoology, 154 (1995), pp. 153-213
[Levi, 1997]
H.W. Levi.
The American orb weavers of the genera Mecynogea, Manogea, Kapogea, and Cyrtophora (Araneae: Araneidae).
Bulletin of the Museum of Comparative Zoology, 155 (1997), pp. 215-255
[Levi, 1999]
H.W. Levi.
The Neotropical and Mexican orb weavers of the genera Cyclosa and Allocyclosa (Araneae: Araneidae).
Bulletin of the Museum of Comparative Zoology, 155 (1999), pp. 299-379
[Levi, 2005]
H.W. Levi.
The orb weaver genus Mangora of Mexico, Central America, and the West Indies (Araneae: Araneidae).
Bulletin of the Museum of Comparative Zoology, 158 (2005), pp. 139-182
[Lubin et al., 1982]
Y.D. Lubin, B.D. Opell, W.E. Eberhard, H.W. Levi.
Orb plus cone-webs in Uloboridae (Araneae), with a description of a new genus and four new species.
Psyche, 89 (1982), pp. 29-64
[Nogueira et al., 2006]
A.A. Nogueira, R. Pinto da Rocha, A.D. Brescovit.
Comunidade de aranhas orbitelas (Arachnida-Araneae) na regiao da Reserva Florestal do Morro Grande, Cotia, Sao Paulo, Brasil.
Biota Neotropica, 6 (2006), pp. 1-24
[Piel, 2001]
W.H. Piel.
The systematics of Neotropical orb-weaving spiders in the genus Metepeira (Araneae: Araneidae).
Bulletin Museum of Comparative Zoology, 157 (2001), pp. 1-92
[Reddell, 1977]
J.R. Reddell.
A preliminary survey of the caves of Yucatán Peninsula.
Association for Mexican Caves Studies Bulletin, 6 (1977), pp. 215-296
[Rico et al., 2005]
A. Rico, A.J.P. Beltrán, D.A. Álvarez, D.E. Flórez.
Diversidad de arañas (Arachnida: Araneae) en el parque nacional natural Isla Gorgona, Pacífico Colombiano.
Biota Netropica, 5 (2005), pp. 1-12
[Rodríguez-Rodríguez et al., 2015]
S.E. Rodríguez-Rodríguez, K.P. Solís-Catalán, A. Valdez-Mondragón.
Diversity and seasonal abundance of anthropogenic spiders (Arachnida: Araneae) in different urban zones of the city of Chilpancingo, Guerrero, Mexico.
Revista Mexicana de Biodiversidad, 86 (2015), pp. 962-971
[Romo and Flórez, 2008]
M.I. Romo, E. Flórez.
Comunidad de arañas orbitelares (Araneae: Orbiculariae) asociada al bosque altoandino del Santuario Flora y Fauna Galeras, Nariño, Colombia.
Boletín Científico Centro de Museos del Museo de Historia Natural, 13 (2008), pp. 114-126
[Russell-Smith and Stork, 1994]
A. Russell-Smith, N.E. Stork.
Abundance and diversity of spiders from the canopy of tropical rainforests with a particular reference to Sulawesi, Indonesia.
Journal of Tropical Ecology, 10 (1994), pp. 545-558
[Silva and Coddington, 1996]
D. Silva, J.A. Coddington.
Spiders of Pakitza (Madre de Dios, Perú): Species richness and notes on community structure.
The biodiversity of Southeastern Peru, pp. 253-311
[Sørensen, 2004]
L.L. Sørensen.
Composition and diversity of spider fauna in the canopy of a montane forest in Tanzania.
Biodiversity and Conservation, 13 (2004), pp. 437-452
[Sutter, 1992]
R. Sutter.
Ballooning: data from spiders in freefall indicate the importance of posture.
Journal of Arachnology, 20 (1992), pp. 107-113
[Valdez-Mondragón, 2006]
A. Valdez-Mondragón.
Diversidad de arañas (Arachnida: Araneae) relacionadas con Las Grutas de Juxtlahuaca, Guerrero, México. Tesis.
Facultad de Ciencias, UNAM, (2006),
[Villaseñor et al., 2005]
J.L. Villaseñor, P. Maeda, J.J. Colín-López, E. Ortiz.
Estimación de la riqueza de especies de Asteraceae mediante extrapolación a partir de datos de presencia-ausencia.
Boletín de la Sociedad Botánica de México, 76 (2005), pp. 518
[World Spider Catalog, 2016]
World Spider Catalog.
World Spider Catalog Version 16.5.
Natural History Museum, (2016),
Retrieved from http://wsc.nmbe.ch

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