Diversidad de Geadephaga (Coleoptera: Carabidae y Cicindelidae) en Colombia: una aproximación desde la literatura existente

Resumen (es):

Las familias Carabidae y Cicindelidae, con cerca de 40 000 especies a nivel mundial, tienen un papel creciente en estudios de biodiversidad y ecología en Colombia, lo que hace necesaria una puesta al día de los conocimientos sobre su diversidad. Presentamos y analizamos la lista de las especies descritas/registradas en Colombia hasta 2020, con base en estudios publicados, y sus datos de distribución a escala de departamento. Los Carabidae están representados por 625 especies y los Cicindelidae por 100. Magdalena, Cundinamarca y Valle del Cauca presentan los mayores números de registros de Carabidae, mientras que para Cicindelidae son Valle del Cauca, Antioquia y Meta. Probablemente, el mayor esfuerzo de muestreo en estas regiones se debe a la accesibilidad de sus áreas naturales desde las principales ciudades. Los Cicindelidae se benefician de más registros de localidad, con solo 17 % de las especies sin mención de localidad específica en el territorio nacional, contra el 40 % en Carabidae. Regiones hiperdiversas, como el Chocó y la Amazonía, están subrepresentadas. Por consiguiente, se estima que el número de especies actualmente citadas es muy inferior a la diversidad real de las dos familias.

Resumen (en):

The beetle families Carabidae and Cicindelidae, with about 40 000 species worldwide, play an increasing role in biodiversity conservation and ecological studies in Colombia, which makes a faunistic update all the more necessary. We present and analyze a checklist of the species so far described or registered from Colombia until 2020, based on published studies, and their distribution data at the department level. Carabidae are represented by 625 species and Cicindelidae by 100. Magdalena, Cundinamarca and Valle del Cauca are the departments with the highest record numbers of Carabidae, while Cicindelidae are most frequently cited from Valle del Cauca, Antioquia and Meta. The greater sampling effort in these regions is likely due to the accessibility of their natural areas from the main towns. The geographical distribution of Cicindelidae is better documented, with only 17 % of the species without mention of specific localities within the country, against 40 % in Carabidae. Hyper-diverse regions, such as the Chocó and the Amazon, are underrepresented. The number of species currently recorded is therefore estimated to be much lower than true diversity for both families.

Palabras clave:

Biodiversity, Faunistics, Ground beetles, Species list, Tiger beetles (en)

Biodiversidad, Escarabajos del suelo, Escarabajos tigre, Faunística, Lista de especies (es)

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Diversity of Geadephaga (Coleoptera: Carabidae and Cicindelidae) in Colombia: an approach from existing literature

https://doi.org/10.21068/2539200X.962

Diversity of Geadephaga (Coleoptera: Carabidae and Cicindelidae) in Colombia: an approach from existing literature

Diversidad de Geadephaga (Coleoptera: Carabidae y Cicindelidae) en Colombia: una aproximación desde la literatura existente

Anderson Arenas-Clavijo 1, James Montoya-Lerma 1 y Pierre Moret 2.

Received: April 7, 2021

Accepted: June 28, 2021

How to cite this article: Arenas-Clavijo, A., Montoya-Lerma, J. & Moret, P. (2022). Diversity of Geadephaga (Coleoptera: Carabidae and Cicindelidae) in Colombia: an approach from existing literature. Biota Colombiana, 22(2), e962.


Abstract

The beetle families Carabidae and Cicindelidae, with about 40 000 species worldwide, play an increasing role in biodiversity conservation and ecological studies in Colombia, which makes a faunistic update all the more necessary. We present and analyze a checklist of the species so far described or registered from Colombia until 2020, based on published studies, and their distribution data at the department level. Carabidae are represented by 625 species and Cicindelidae by 100. Magdalena, Cundinamarca and Valle del Cauca are the departments with the highest record numbers of Carabidae, while Cicindelidae are most frequently cited from Valle del Cauca, Antioquia and Meta. The greater sampling effort in these regions is likely due to the accessibility of their natural areas from the main towns. The geographical distribution of Cicindelidae is better documented, with only 17 % of the species without mention of specific localities within the country, against 40 % in Carabidae. Hyper-diverse regions, such as the Chocó and the Amazon, are underrepresented. The number of species currently recorded is therefore estimated to be much lower than true diversity for both families.

Key words. Biodiversity. Faunistics. Ground beetles. Species list. Tiger beetles.


Resumen

Las familias Carabidae y Cicindelidae, con cerca de 40 000 especies a nivel mundial, tienen un papel creciente en estudios de biodiversidad y ecología en Colombia, lo que hace necesaria una puesta al día de los conocimientos sobre su diversidad. Presentamos y analizamos la lista de las especies descritas/registradas en Colombia hasta 2020, con base en estudios publicados, y sus datos de distribución a escala de departamento. Los Carabidae están representados por 625 especies y los Cicindelidae por 100. Magdalena, Cundinamarca y Valle del Cauca presentan los mayores números de registros de Carabidae, mientras que para Cicindelidae son Valle del Cauca, Antioquia y Meta. Probablemente, el mayor esfuerzo de muestreo en estas regiones se debe a la accesibilidad de sus áreas naturales desde las principales ciudades. Los Cicindelidae se benefician de más registros de localidad, con solo 17 % de las especies sin mención de localidad específica en el territorio nacional, contra el 40 % en Carabidae. Regiones hiperdiversas, como el Chocó y la Amazonía, están subrepresentadas. Por consiguiente, se estima que el número de especies actualmente citadas es muy inferior a la diversidad real de las dos familias.

Palabras clave. Biodiversidad. Escarabajos del suelo. Escarabajos tigre. Faunística. Lista de especies


Introduction

Geadephaga, the group of terrestrial Adephaga formed by Carabidae (ground beetles), Cicindelidae (tiger beetles) and Trachypachidae, with about 40 000 described species worldwide, represents nearly 10 % of the species so far described in the order Coleoptera (Bouchard et al., 2017; Lorenz, 2017). Within this monophyletic group (López-López & Vogler, 2017), the position of tiger beetles is still under debate, whether as Cicindelidae at family rank (López-López & Vogler, 2017; Duran & Gough, 2020) or as Cicindelinae within Carabidae (Gough et al., 2019; Li et al., 2020). In this study, we provisionally placed tiger beetles at family rank without prejudice to future advances in genomic studies, because in most studies they have been treated separately from ground beetles. Trachypachidae, on their part, are not represented in the Neotropics.

Carabidae and Cicindelidae are present in almost every possible ecosystem worldwide (Lövei & Sunderland, 1996), with a great diversity of life history traits, and frequently used as bioindicators in ecological studies (Rainio & Niemelä, 2003; Pearce & Venier, 2006) or as control agents against agricultural pests, due to their predatory habits (Kromp, 1999; de Heij & Willenborg, 2020). Therefore, their knowledge can be crucial in studies on sustainable agriculture, or on assessment of vulnerable natural areas.

Information on Geadephaga of Colombia has been synthetized in two studies more than fifteen years ago: one by Vítolo (2004) on Cicindelidae, and another by Martínez (2005) on Carabidae. Vítolo (2004) offers data on morphology, distribution in Colombia, identification keys, and a summary of the diversity of tiger beetles in the country. Martínez (2005) provides identification keys with full habitus illustrations for all the genera present in Colombia. As the main objective of the latter study was to allow identification at the genus level, the information on the distribution of taxa was also limited to genera. Moreover, the list of species in Martínez (2005) needs revision in three aspects: some species cited from Colombia in the scientific literature were not included, the presence in Colombia of other species is stated without references, and a few unnamed morphospecies are listed, which hinders a correct evaluation of the total number of species cited from Colombia. As a complement to these fundamental works, Moret (2003) published an identification key to the Carabidae of the Andean paramo which includes southern Colombia, but it is also limited to genera and does not provide any distributional information.

In Colombia, the uncertainty about the identity of many species (Linnaean shortfall) and their spatial distribution (Wallacean shortfall) are the greatest obstacles to develop robust ecological studies (Hortal et al., 2015). In addition, poor taxonomic and faunistic knowledge limits the potential assessment of the ecosystem services that these beetles could provide. Parataxonomy (i.e. the assignation of individuals to morphospecies based on their external appearance, without considering neither taxonomic literature nor the specialists within the group), as an alternative way to overcome the taxonomic impediment in ecological studies, appears to be an unsatisfactory solution, since it tends to overestimate the number of species and does not guarantee reproducibility (Krell, 2004).

The knowledge of Colombian Geadephaga has increased in recent years, due to a growing number of taxonomic (e.g. Arenas-Clavijo, 2017; Forero et al., 2019; Moret, 2019; Sarmiento-Roa et al., 2020) and ecological studies (e.g. Arenas & Armbrecht, 2019; García-Suabita et al., 2019) based on this group during the last decade. An update of the current taxonomic and faunistic knowledge was therefore necessary, as a starting point for future systematic revisions of the tribes or genera which might deserve special attention from a biogeographical or ecological point of view.

For these reasons, the present study aims to list the Carabidae and Cicindelidae species recorded from Colombia in the literature, up to 2020, thus offering a current state of knowledge of these two families, emphasizing gaps and biases. It also seeks to provide information on areas of potential interest, where it would be convenient to intensify, complete or initiate samplings of these ecologically important beetles.

Material and methods

Bibliographic database

A total of 150 studies published up to 2020, related to ground and tiger beetles of Colombia, was obtained from an exhaustive search that included documents from the 19th century. Much of this literature is available in electronic repositories (e.g. Biodiversity Heritage Library, Gallica, Persée), and a smaller portion was gathered by direct request to libraries or authors. The reviewed publications cover the following topics: (1) descriptions of new species based on material from Colombia or, in the mid-19th century studies, from “Nueva Granada” or “Nouvelle Grenade”; (2) new Colombian records of species already described from other countries; (3) lists of species of a genus or of a supra-generic taxon in systematic revisions; and (4) ecological studies or biodiversity inventories. Regarding the last category, doubtful attributions marked as “cf.” or “aff.”, as well as morphospecies designated by a number, were not included. Based on this inventory, the references of all the species listed by Martínez (2005) were verified (Appendix 1), and a new checklist was produced.

Construction of the checklist

Once the references were compiled, a list was constructed in which species are sorted by genus. Infraspecific taxa were excluded from the list. Generic and subgeneric names were updated in accordance with Lorenz (2017) or based on the last available systematic revisions. In the case of synonyms or debated generic attribution, we followed as a general rule the taxonomic decision of the most recent revision, the reference of which is given in the bibliographic section of the list (Appendix 2, last column). Locality information is limited to the “Departamento” (department or province), and only published localities were taken into account.

Data analysis

The checklist was used as a database to build graphs and maps to better understand the current state of knowledge of the group in Colombia. These graphs are based on the description year or on the year of the first record for each species, on the number of species per genus, and on the number of species per department.

Results

Carabidae

Based on published data, the family Carabidae is currently represented in Colombia by 625 species —close to 1.7 % of the world total—, arranged in 10 subfamilies, 32 tribes and 125 genera (Appendix 2). Of the recorded species, 330 (53 %) have not been reported from any other country, so that could be considered Colombian endemics, at least until they do not get recorded from any surrounding country. Thirteen genera account for 50 % of the species, the most speciose genus being Dyscolus Dejean, 1831 (Harpalinae, Platynini), which contains 14 % of the total (85 species) (Figure 1). Forty-seven genera (38 %) are represented by a single species in Colombia (Table 1), five of which are monospecific, with records of their unique species in at least another country: Stenocheila (Harpalinae, Lachnophorini); Askalaphium (Harpalinae, Ctenodactylini); Enceladus (Siagoninae, Siagonini); Homalomorpha (Harpalinae, Cratocerini) and Trichognatha (Harpalinae, Galeritini) (Martínez 2003, 2005; Martínez & Ball, 2003; Lorenz, 2017). Three genera are only known from Colombia: Callidadelpha (Harpalinae, Lebiini), Cryptomma (Scaritinae, Clivinini) (without specific locality recorded) and Columbitrechus (the latter, most likely a synonym of Paratrechus). Finally, two introduced species have been registered: Laemostenus complanatus, from northern Africa and/or western Europe (Martínez, 2005), and Mochtherus tetraspilotus, from southeastern Asia (Torres-Domínguez et al., 2020).


Figure 1. Number and proportion of species by genus of ground beetles recorded from Colombia.

Table 1. Structure of the subfamilies and tribes of Carabidae Latreille, 1802 in Colombia. In parentheses: number of genera with only one species recorded in the country.

Subfamily

Tribe

Number of genera

Number of species

Brachininae Bonelli, 1810

Brachinini Bonelli, 1810

2

7

Carabinae Latreille, 1802

Carabini Latreille, 1802

1

5

Harpalinae Bonelli, 1810

Cratocerini Lacordaire, 1854

3 (2)

6

Chaetogenyini Bonelli, 1813

1(1)

1

Ctenodactylini Laporte de Castelnau, 1834

3 (2)

6

Cyclosomini Laporte de Castelnau, 1834

2

8

Dercylini Bonelli, 1813

1

3

Galeritini LeConte, 1853

2 (1)

8

Harpalini Bonelli, 1810

11 (4)

52

Helluonini Bonelli, 1813

4 (2)

6

Lachnophorini LeConte, 1853

9 (5)

24

Lebiini Bonelli, 1810

26 (9)

178

Morionini Brullé, 1834

2 (1)

5

Odacanthini Laporte de Castelnau, 1834

5 (1)

34

Peleciini Chaudoir, 1880

1

2

Perigonini Horn, 1881

2 (2)

2

Platynini Bonelli, 1810

5 (1)

102

Pterostichini Bonelli, 1810

8 (2)

34

Sphodrini Laporte de Castelnau, 1834

1 (1)

1

Zuphiini Bonelli, 1810

2 (1)

4

Licininae Bonelli, 1810

Chlaeniini Brullé, 1834

1

3

Melaeninae Alluaud, 1934

Melaenini Csiki, 1933

1 (1)

1

Paussinae Latreille, 1807

Ozaenini Hope, 1838

3 (1)

11

Paussini Latreille, 1806

1

3

Rhysodinae Laporte de Castelnau, 1840

Rhysodini Laporte de Castelnau, 1840

1

12

Scaritinae Bonelli, 1810

Clivinini Rafinesque, 1815

8 (3)

40

Forcipatorini Bänninger, 1937

3 (2)

4

Scaritini Bonelli, 1810

4 (1)

11

Siagoninae Bonelli, 1813

Siagonini Bonelli, 1813

1 (1)

1

Trechinae Bonelli, 1810

Bembidiini Stephens, 1827

6

37

Pogonini Laporte de Castelnau, 1834

1 (1)

1

Trechini Bonelli, 1810

4 (2)

13

Regarding species geographic distribution, 254 species (~41 %) are known from the country as a whole without more precise localities, from which 143 have not been cited from any other country; 371 species (~59 %) have at least one specific locality record. 309 species are known from a single department, and 163 of these are exclusive to Colombia. The departments with the highest number of recorded species are: Magdalena (79), Cundinamarca (75) and Valle del Cauca (43), while Guaviare, San Andrés y Providencia and Sucre have no records for the family (Appendix 1, Figures 2 and 3).


Figure 2. Number of ground beetle species per Colombian departments.


Figure 3. Number of ground beetle species per Colombian department, based on data published from 1831 to 2020.

The species with the widest distribution in Colombia are Laemostenus (Laemostenus) complanatus (Harpalinae, Sphodrini) and Pelmatellus variipes (Harpalinae, Harpalini), each one with locality data in 11 departments (Camero, 2003; Martínez & Ball, 2003), but most of the species with the widest distribution belong to the tribe Platynini. However, in some cases, systematic revisions could reveal the existence of several species with more limited distributions under the currently accepted name.

Cicindelidae

The family Cicindelidae is currently represented in Colombia by 100 species distributed in three tribes and 21 genera of the subfamily Cicindelinae (Appendix 3). This figure represents 3.3 % of the world total of tiger beetle species, a percentage twice as high as in Carabidae. Of the species registered in the Colombian territory, 16 do not have records in any other country, most of them probably endemic according to the available data. The most diverse genus is Odontocheila, with 16 species, while 81 % of the remaining species is contained in seven different genera (Figure 4).


Figure 4. Number and proportion of species by genus of tiger beetle recorded from Colombia.

Eight tiger beetle genera are represented by a single species in Colombia (Table 2), but none has a distribution limited to the country. Callidema boussingaulti (Cicindelini) has a restricted distribution in mountain environments, since it is known only from the Andes of Colombia, Peru and Ecuador (Cassola & Pearson, 2001). Other genera such as Cheiloxya (Cicindelini), Cenothyla (Cicindelini) and Ronhuberia (Cicindelini) are distributed in northern South America (Cassola & Pearson, 2001; Moravec, 2020).

Table 2. Structure of the subfamilies and tribes of Cicindelidae Latreille, 1802 in Colombia. In parentheses: number of genera with only one species recorded in the country.

Subfamily

Tribe

Number of genera

Number of species

Cicindelinae Latreille, 1802

Cicindelini Latreille, 1802

13 (5)

54

Ctenostomatini, Laporte de Castelnau, 1834

1

8

Megacephalini Laporte de Castelnau, 1834

4 (2)

13

Oxycheilini Chaudoir, 1860

3 (1)

25

Regarding the distribution of Cicindelidae in Colombia, 17 species (17 %) do not have any precise locality records, three of which appear to be endemic to the country: Odontocheila simulator, although the holotype and only known specimen of this dubious taxon is probably an artefact (Moravec, 2018); Pseudoxycheila ceratoma; and Pseudoxycheila tarsalis (Cicindelini). 21 species are known from only one department (Figure 5), and of these, four are not recorded from other countries: Odontocheila hamulipenis and Oxycheila pseudoaquatica (Cicindelini) from Valle del Cauca; Oxygonia kippenhani from Boyacá; and Ctenostoma (Procephalus) maculosum (Ctenostomatini) from Cundinamarca (Appendix 3).


Figure 5. Distribution of tiger beetle species in Colombia, per departments.

The departments with the highest number of tiger beetle species records are Valle del Cauca (36), Antioquia (27) and Meta (27), whereas San Andrés, Providencia and Arauca do not have records (Appendix 3 and Figure 6). Vaupés department, with only one record (Odontocheila trilbyana), is located in the Amazonia, a region where many tiger beetle species have already been reported in neighboring countries, which highlights the low level of sampling of this ecosystem in Colombia.


Figure 6. Number of tiger beetle species per Colombian department, based on data published from 1842 to 2020.

The species with the widest distribution in Colombia are Pseudoxycheila bipustulata, with records in 20 departments, and Tetracha (Tetracha) sobrina in 19 (Appendix 3). Regarding the genus Pseudoxycheila Vítolo (2004) expressed doubts about the status of some species proposed by Cassola (1997), as species differentiation is especially difficult in this Andean genus, and several of the new species described by Cassola appear to fall within the morphological variation range of P. bipustulata. In this case, as in many others, a molecular approach would be necessary to solve the issues left by conventional morphology-based taxonomy.

Discussion

The current knowledge of the families Carabidae and Cicindelidae in Colombia is the result of a two centuries-long history (Figure 7). Regarding Carabidae, taxonomic descriptions based on material from Colombia began as early as 1825, but they reached their greatest development between the second third and the end of the 19th century, a period in which 70 % of the carabid fauna known from the country had already been described, mainly thanks to the contributions of Louis Reiche (52 species described between 1842 and 1843), Maximilien de Chaudoir (131 species described between 1848 and 1880) and Jules Putzeys (89 species described between 1846 and 1878). In this period, most descriptions were very brief, not illustrated, with limited distribution data or without any, and they did not fit the current standards of insect taxonomy. Furthermore, very few have been subject to taxonomic revisions in recent times, which makes their identification difficult, if not impossible without examining type specimens. The genera in which this situation is especially detrimental are Dyscolus, Notiobia, Lebia and Agra, among others. From the beginning of the twentieth century, the rate of description of new species has been very slow, with a slight rebound from 1980. The new records from Colombia (i.e. for species whose description was based on specimens from other countries) have followed a much slower pace, with a gradual increase from the mid-20th century, when authors such as Stefano Straneo (records from Colombia from 1951 to 1991), Joaquim Mateu (1961-1998), George E. Ball (1978-2013), Terry L. Erwin (1970-2016), Danny Shpeley (1978-2013), among others, contributed to the knowledge of the fauna of Colombia.


Figure 7. Cumulative number of ground beetle species described (in blue) and recorded from Colombia (in orange), in five-years increments, up to 2020. Species described from Colombia but subsequently synonymized are not included.

The investigations on Cicindelidae followed a different path (Figure 8). The pace of descriptions was globally slow, with two acceleration points: a weak one during the second third of the 19th century, with contributions by several authors who published isolated species descriptions, and another very strong in the last decade of the twentieth century, based on more comprehensive works, especially revisions of genera at a continent scale, such as those by Cassola (1997), Naviaux (1998), Wiesner (1992, 1999). Thanks to these taxonomic revisions and to several local, national or continental checklists (Cassola & Pearson, 2001; Fernández et al., 1993; Moravec 2018, 2020; Vítolo & Pearson, 2003; Wiesner, 2020), Colombian records of species described from other countries increased dramatically since 1990, exceeding the number of new descriptions. In this regard, tiger beetle knowledge has progressed much faster in recent decades than that of ground beetles. This greater sampling and publication effort may also explain why the Colombian records amount to 3.3 % of the world total of tiger beetle species, a percentage twice as high as in Carabidae.


Figure 8. Cumulative number of tiger beetle species described from Colombia (in blue) and recorded from Colombia (in orange), in five-year increments, up to 2020. Species described from Colombia but subsequently synonymized are not included.

The geographical distribution of the locality records of Carabidae (Figure 3) is largely due to accessibility factors. In most cases, naturalists of the 19th century and the first half of the 20th century were constrained by the reduced transportation network of that time and collected along the same routes around the main cities. Natural areas near main roads and navigable rivers were the most surveyed, which creates an over-sampling bias and makes it difficult to assess the true diversity of each region, in line with the results of a study performed in a neighboring country (Donoso et al., 2009). Another kind of bias derives from the activity of a particular researcher in a limited area. For example, most of the species reported from the Magdalena department correspond to species of the genus Blennidus, described by Stefano Straneo from specimens collected by Philip J. Darlington in the Sierra Nevada de Santa Marta in 1928 and 1929. Conversely, ground beetle diversity is clearly underestimated in less accessible hyper-diverse regions such as the Chocó ecoregion, the Amazon foothills (Caquetá and Putumayo departments) and the Amazon rainforest itself (Guainía, Guaviare and Vaupés departments). Although true diversity cannot be precisely assessed based on available data, it is expected that these regions have a more diverse carabid fauna than what is currently known.

The distribution of tiger beetle records throughout the Colombian territory (Figure 6) is more balanced than that of ground beetles, possibly due to the interest the group has provoked among professional and amateur entomologists over the last decades.

When comparing the number of Geadephaga species recorded so far from Colombia (725) with that of other countries, it appears clearly that there is still a huge work ahead before approaching a complete knowledge of their diversity in this country. Our results in Colombia are comparable to those obtained in Peru, where 690 species are currently known (Erwin et al., 2015, leaving aside unnamed morphospecies only designated by numbers) in a territory of a size similar to that of Colombia. In Brazil, a territory eight times larger, 1506 species have been reported, that is, only twice as many (Roig Juñent & Domínguez, 2001). The level of knowledge is higher in Ecuador, with 763 species (Moret & Salazar, unpublished data) in a territory five times smaller and in ecosystems shared with southern Colombia: Chocó ecoregion, Andean montane forest, paramo, interandean dry shrublands or woodlands, Amazonian lowlands. Outside the Neotropics, to mention just one example, 693 species have been reported in the state of Texas in the United States of America (Bousquet, 2012), a territory twice as small.

The magnitude of the work to be done is obvious when noting that the late Terry L. Erwin collected more than 600 species of Carabidae (most of which remain undescribed) in the Pakitza reserve of Peruvian Amazonia, in a space of only 40 km2 (Erwin, 1991), that is, a number close to the total of the described species registered for the whole of Peru. In Colombia, the number of recorded species does not exceed 42 in any of the six departments (Nariño, Putumayo, Caquetá, Cauca, Huila, Meta) which contain environments similar to that of Pakitza, i.e. lower montane forest at an elevation of about 650 m in the Amazonian foothills of the Andes.

Conclusion and perspectives

The results of this study suggest that the deficient taxonomic and chorological knowledge of the families Carabidae and Cicindelidae in Colombia will be an obstacle to developing well supported ecological studies of this group, as long as species distributions are not accurately known. Publication of distributional information based on reliable identifications, as well as taxonomic revisions of the genera offering the highest value as bioindicators or pest control, are therefore urgent priorities.

Another challenge faced by the study of Geadephaga in Colombia is the possibility of reaching the specific level in identifications, an issue that can be of great importance in ecological studies. The identification keys currently available for Colombia (Moret, 2003; Martínez, 2005; Vítolo, 2004) are limited to the genus level. Species-level keys exist for a number of neotropical genera (e.g. Arndt, 1998; Ball & Shpeley, 2009; Boyd & Erwin, 2016), but they include species not found in Colombia and are therefore difficult to use by non-taxonomic biologists. Developing keys for all genera of ground beetles and tiger beetles recorded in Colombia is currently an unachievable goal, but it would be desirable to focus efforts on a small number of genera including a sufficient number of described species and of interest as bioindicators.

Finally, in the light of current knowledge and the available techniques, two paths are needed to improve future studies of ground beetles in Colombia: (1) compare specimens deposited in Colombian collections with types kept in European and North American museums, to generate valid vouchers for local taxonomists, and (2) retrieve molecular data (e.g. COI-based DNA barcodes) from these local vouchers, to facilitate future research.

Acknowledgments

We warmly thank Jiri Moravec for providing recent literature on Odontocheilina (Cicindelidae), Petr Bulirsch for useful comments on the systematics of Scaritinae (Carabidae), and Fernanda Salazar for her help in the construction of the database and information on the Ecuadorian carabid fauna. We especially thank Dione Seriperri, Museu de Zoologia, Universidade de São Paulo, for her help in finding publications by Hans Reichardt. AAC’s doctoral studies were partly funded by the “Fondo nacional de financiamiento para la ciencia, la tecnología y la innovación, Francisco José de Caldas”, contract number 491-2020 in program 1106-852-70306 “Relaciones multiescalares de la diversidad en gradientes altitudinales del bosque tropical”, project 70899 “Diversidad de artrópodos en gradientes altitudinales: una aproximación integrativa morfológica y molecular”. Finally, but not last, we thank the comments of two anonymous reviewers, which helped to improve the manuscript.

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Appendix 1. Bibliographic references reviewed to generate the species list of Geadephaga present in Colombia.

Appendix 2. List of species of Carabidae Latreille, 1802 recorded from Colombia until 2020, with their respective distribution within the country. Species marked with asterisk (*) have been cited only from Colombia. Departments are codified according to ISO rule 3166-2. References are listed in appendix 1.

Subfamily

Tribe

Genus

Species

Department

Reference

Brachininae Bonelli, 1810

Brachinini Bonelli, 1810

Brachinus Weber, 1801

Brachinus (Neobrachinus) aeger Chaudoir, 1876

No data

Erwin, 1970

Brachinus (Neobrachinus) geniculatus Dejean, 1831

BOL

Dejean, 1831

Brachinus (Neobrachinus) lateralis Dejean, 1831

No data

Bates, 1883

Brachinus (Neobrachinus) limbiger Chaudoir, 1876

No data

Chaudoir, 1876a

Brachinus (Neobrachinus) olidus Reiche, 1843*

No data

Reiche, 1843a

Pheropsophus Solier, 1833

Pheropsophus (Pheropsophus) aequinoctialis (Linnaeus, 1763)

MAG

Bates, 1883; Arenas-Clavijo & Posso-Gómez, 2017

Pheropsophus (Pheropsophus) rivierii (Demay, 1838)

No data

Chaudoir, 1876a

Carabinae Latreille, 1802

Carabini Latreille, 1802

Calosoma Weber, 1801

Calosoma (Carabosoma) angulatum Chevrolat, 1834

MAG

Gidaspow, 1963

Calosoma (Carabosoma) glabratum Dejean, 1831

CUN

Gidaspow, 1963

Calosoma (Castrida) abbreviatum Chaudoir, 1869

VAC

Gidaspow, 1963

Calosoma (Castrida) alternans (Fabricius, 1792)

VAC

Gidaspow, 1963; Arenas-Clavijo & Posso-Gómez, 2017

Calosoma (Castrida) fulgens Chaudoir, 1869

VAC

Gidaspow, 1963

Harpalinae Bonelli, 1810

Cratocerini Lacordaire, 1854

Catapiesis Solier, 1835

Catapiesis attenuata (Chaudoir, 1862)

No data

Reichardt, 1973

Catapiesis brasiliensis (Gray, 1832)

No data

Reichardt, 1973

Catapiesis columbica Chevrolat, 1838*

No data

Reichardt, 1973

Catapiesis tumida Reichardt, 1973*

CUN

Reichardt, 1973

Cratocerus Dejean, 1829

Cratocerus indupalmensis Grzymala & Will, 2014

CES

Grzymala & Will, 2014

Homalomorpha Brullé, 1835

Homalomorpha castanea Brullé, 1835

No data

Chaudoir, 1852

Chaetogenyini Bonelli, 1813

Camptotoma Reiche, 1843

Camptotoma lebasii Reiche, 1843*

No data

Reiche, 1843b

Ctenodactylini Laporte de Castelnau, 1834

Amblycoleus Chaudoir, 1872

Amblycoleus platyderus (Chaudoir, 1861)

COR

Chaudoir, 1861

Askalaphium Liebke, 1938

Askalaphium depressum (Bates, 1871)

PUT

Martínez, 2003

Leptotrachelus Latreille, 1829

Leptotrachelus aequinoctialis (Chaudoir, 1848)*

No data

Chaudoir, 1848

Leptotrachelus fulvicollis Reiche, 1842*

No data

Reiche, 1842b

Leptotrachelus setulosus Liebke, 1928

No data

Mroczkowski, 1960

Leptotrachelus testaceus Dejean, 1831

BOL

Dejean, 1831; Chaudoir, 1848

Cyclosomini Laporte de Castelnau, 1834

Anaulacus MacLeay, 1825

Anaulacus (Aephnidius) piceolus (Chaudoir, 1876)

BOL, MAG

Ball & Shpeley, 2002

Anaulacus (Macracanthus) ciliatus (Mutchler, 1934)

VID

Ball & Shpeley, 2002

Anaulacus (Macracanthus) sericatus (Chaudoir, 1846)

MAG

Ball & Shpeley, 2002

Tetragonoderus Dejean, 1829

Tetragonoderus (Peronoscelis) undatus Dejean, 1829

CAQ

Martínez, 2003

Tetragonoderus (Peronoscelis) variegatus Dejean, 1829

No data

Chaudoir, 1876b

Tetragonoderus (Peronoscelis) velutinus Motschulsky, 1864

GUA

Martínez, 2003

Tetragonoderus (Tetragonoderus) quadriguttatus Dejean, 1829

HUI, MAG, TOL

Martínez, 2003; Shpeley & Ball, 2008

Tetragonoderus (Tetragonoderus) tesselatus Chaudoir, 1876

MAG

Martínez, 2003

Dercylini Bonelli, 1813

Dercylus Laporte de Castelnau, 1832

Dercylus (Dercylus) alternans Kuntzen, 1912

No data

Kuntzen, 1912

Dercylus (Dercylus) opacus Kuntzen, 1912

No data

Kuntzen, 1912

Dercylus (Licinodercylus) tuberculatus (Chaudoir, 1883)*

CAL, CAU

Moret & Bousquet, 1995

Galeritini LeConte, 1853

Galerita Fabricius, 1801

Galerita (Galerita) aequinoctialis Chaudoir, 1852

BOL

Martínez, 2003

Galerita (Galerita) amazonica Liebke, 1939

ARA, BOY, CAS, CUN, MAG, MET, VID

Camero, 2003

Galerita (Galerita) americana (Linnaeus, 1758)

VAC, VID

Arenas et al., 2013, García-Suabita et al., 2019

Galerita (Galerita) moritzi Mannerheim, 1837

MET, HUI, VAC

Reichardt, 1967; Arenas-Clavijo & Posso-Gómez, 2017

Galerita (Galerita) mustelina Bates, 1884

RIS

Reichardt, 1967

Galerita (Galerita) occidentalis (Olivier, 1795)

RIS, VAC

Reichardt, 1967; Arenas-Clavijo & Posso-Gómez, 2017

Galerita (Galerita) tristis Reiche, 1842

ATL, MAG

Reichardt, 1967

Trichognatha Latreille, 1829

Trichognatha marginipennis Latreille, 1829

BOY

Reichardt, 1967; Steinheil, 1875a

Harpalini Bonelli, 1810

Amblygnathus Dejean, 1829

Amblygnathus darlingtoni Ball & Maddison, 1987

MAG

Ball & Maddison, 1987

Amblygnathus janthinus Dejean, 1829

No data

Ball & Maddison, 1987

Amblygnathus suturalis Putzeys, 1845

ATL

Sarmiento-Roa et al., 2020

Anisocnemus Chaudoir, 1843

Anisocnemus amblygonus Shpeley & Ball, 1978

ATL, CES

Shpeley & Ball, 1978

Anisocnemus validus Chaudoir, 1843*

No data

Shpeley & Ball, 1978

Athrostictus Bates, 1878

Athrostictus circumfusus (Putzeys, 1878)*

No data

Putzeys, 1878a

Athrostictus luridus (Reiche, 1843)

No data

Putzeys, 1878a

Athrostictus paganus (Dejean, 1831)

BOL, CAU

Dejean, 1831; Putzeys, 1878a; Arenas & Armbrecht, 2019

Athrostictus velutinus (Putzeys, 1878)*

No data

Putzeys, 1878a

Bradycellus Erichson, 1837

Bradycellus (Bradycellus) apicalis Putzeys, 1878*

CUN

Putzeys, 1878b

Bradycellus (Bradycellus) celeripes Putzeys, 1878*

CUN

Putzeys, 1878b

Bradycellus (Bradycellus) suturiger Putzeys, 1878*

ATL

Putzeys, 1878b

Neoaulacoryssus Noonan, 1985

Neoaulacoryssus cupripennis (Gory, 1833)

TOL

Sarmiento-Roa et al., 2020

Notiobia Perty, 1830

Notiobia (Anisotarsus) praeclara Putzeys, 1878*

CAU, CUN, VAC

Noonan, 1981; Arenas-Clavijo, 2017

Notiobia (Notiobia) aeneola Putzeys, 1878*

ATL

Putzeys, 1878b

Notiobia (Notiobia) aulica (Dejean, 1829)

ARA, BOY, CAU, CES, CUN, MAG, QUI, TOL

Arndt, 1998; Camero, 2003

Notiobia (Notiobia) concolor Putzeys, 1878*

CAL, CUN, NSA

Putzeys, 1878b

Notiobia (Notiobia) disparilis Bates, 1878

CAQ

Sarmiento-Roa et al., 2020

Notiobia (Notiobia) dubia Putzeys, 1878*

ATL

Putzeys, 1878b

Notiobia (Notiobia) glabrata Arndt, 1998

CAQ

Sarmiento-Roa et al., 2020

Notiobia (Notiobia) jucunda Putzeys, 1878

CUN

Putzeys, 1878b

Notiobia (Notiobia) longipennis Putzeys, 1878*

No data

Putzeys, 1878b

Notiobia (Notiobia) similis Putzeys, 1878*

CAL, CUN

Putzeys, 1878b

Notiobia (Notiobia) umbrifera Bates, 1884

CAU, VAC

Arenas-Clavijo, 2017

Pelmatellus Bates, 1882

Pelmatellus columbianus (Reiche, 1843)

BOY, CAL, CUN, SAN

Moret, 2000

Pelmatellus variipes Bates, 1891

AMA, ARA, BOY, CAL, CUN, MAG, MET, QUI, SAN, VAU, VID

Camero, 2003

Polpochila Solier, 1849

Polpochila (Polpochila) marginalis Nègre, 1963

MAG

Nègre, 1963

Selenophorus Dejean, 1829

Selenophorus (Celiamorphus) discopunctatus Dejean, 1829

No data

Reiche, 1843c

Selenophorus (Selenophorus) aurichalceus Dejean, 1831*

BOL

Dejean, 1831; Putzeys, 1878a

Selenophorus (Selenophorus) coracinus Dejean, 1831*

BOL

Dejean, 1831

Selenophorus (Selenophorus) cyaneus Putzeys, 1878*

No data

Putzeys, 1878a

Selenophorus (Selenophorus) dilutipes Putzeys, 1878

No data

Putzeys, 1878a

Selenophorus (Selenophorus) dimidiatulus van Emden, 1958*

MAG

van Emden, 1958

Selenophorus (Selenophorus) distinctus Putzeys, 1878*

No data

Putzeys, 1878a

Selenophorus (Selenophorus) exilis Dejean, 1831*

BOL, MAG

Dejean, 1831; Putzeys, 1878a

Selenophorus (Selenophorus) irideus Reiche, 1843*

No data

Reiche, 1843c

Selenophorus (Selenophorus) irinus (Reiche, 1843)

No data

Reiche, 1843d; Putzeys, 1878a

Selenophorus (Selenophorus) laevicollis (Bates, 1884)

No data

Bates, 1883

Selenophorus (Selenophorus) liodiscus Putzeys, 1878*

No data

Putzeys, 1878a

Selenophorus (Selenophorus) modestus Putzeys, 1878*

No data

Putzeys, 1878a

Selenophorus (Selenophorus) myrmidon Dejean, 1831*

BOL

Dejean, 1831; Putzeys, 1878a

Selenophorus (Selenophorus) pyritosus Dejean, 1829

MAG, BOL

Martínez, 2003

Selenophorus (Selenophorus) ruficollis (Putzeys, 1878)

AMA

Ball & Maddison, 1987

Selenophorus (Selenophorus) splendidus Putzeys, 1878

No data

Putzeys, 1878a

Selenophorus (Selenophorus) striatopunctatus Putzeys, 1878

BOL

Martínez, 2003

Selenophorus (Selenophorus) subaeneus Reiche, 1843

No data

Reiche, 1843c

Selenophorus (Selenophorus) vicinus Dejean, 1829

No data

Putzeys, 1878a

Selenophorus (Selenophorus) xantholomus Putzeys, 1878

No data

Putzeys, 1878a

Selenophorus (Selenophorus) affinis Dejean, 1831

No data

Putzeys, 1878a

Selenophorus (Selenophorus) brevis (Putzeys, 1878)*

TOL

Putzeys, 1878a

Stenomorphus Dejean, 1831

Stenomorphus angustatus Dejean, 1831

BOL

Ball et al., 1991

Trichopselaphus Chaudoir, 1843

Trichopselaphus magnificus Ball, 1978

VAC

Sarmiento-Roa et al., 2020

Helluonini Bonelli, 1813

Dailodontus Reiche, 1843

Dailodontus clandestinus (Klug, 1834)

MAG, VAC

Reichardt, 1974b; Arenas-Clavijo & Chacón de Ulloa, 2016

Helluobrochus Reichardt, 1974

Helluobrochus cribratus (Reiche, 1843)

AMA, BOY, VID

Reiche, 1843a; Reichardt, 1974b

Helluobrochus subrostratus (Bates, 1871)

CAS

Martínez, 2003

Helluomorphoides Ball, 1951

Helluomorphoides glabratus (Bates, 1871)

No data

Reichardt, 1974b

Helluomorphoides unicolor (Brullé, 1838)

AMA

Martínez, 2003

Pleuracanthus Gray, 1832

Pleuracanthus sulcipennis Gray, 1832

MET

Martínez, 2003

Lachnophorini LeConte, 1853

Amphithasus Bates, 1871

Amphithasus elegans (Dejean, 1831)*

BOL

Zamorano et al., 2019

Anchonoderus Reiche, 1843

Anchonoderus apicalis Reiche, 1843*

No data

Reiche, 1843b

Anchonoderus binotatus Reiche, 1843

No data

Reiche, 1843b

Anchonoderus cyanescens (Putzeys, 1878)*

BOY

Putzeys, 1878b; Zamorano et al., 2019

Anchonoderus erosus Putzeys, 1878*

No data

Putzeys, 1878b

Anchonoderus femoratus Putzeys, 1878*

BOY

Putzeys, 1878b

Anchonoderus myops Reiche, 1843

No data

Reiche, 1843b

Anchonoderus reichei Putzeys, 1878*

ANT, BOY, CUN NSA

Putzeys, 1878b

Anchonoderus subaeneus Reiche, 1843

No data

Reiche, 1843b

Anchonoderus unicolor Chaudoir, 1850*

No data

Chaudoir, 1850

Asklepia Liebke, 1938

Asklepia laetitia Zamorano & Erwin, 2014*

AMA

Erwin & Zamorano, 2014

Calybe Laporte de Castelnau, 1834

Calybe grata (Motschulsky, 1864)

No data

Motschulsky, 1864

Ega Laporte de Castelnau, 1835

Ega aequatoria Chaudoir, 1850*

No data

Chaudoir, 1850

Ega delicatula (Motschulsky, 1864)*

No data

Motschulsky, 1864

Euphorticus Horn, 1881

Euphorticus laevicollis (Reiche, 1843)

No data

Zamorano et al., 2019

Lachnophorus Dejean, 1831

Lachnophorus angusticollis Putzeys, 1878*

ANT

Putzeys, 1878b

Lachnophorus maculatus Chaudoir, 1850*

No data

Chaudoir, 1850

Lachnophorus pictipennis Bates, 1871

MAG

Martínez, 2003

Lachnophorus sabanillae Liebke, 1936

No data

Liebke, 1936

Lachnophorus signatipennis Chaudoir, 1850*

No data

Chaudoir, 1850

Peruphorticus Erwin & Zamorano, 2014

Peruphorticus pallipes (Reiche, 1843)*

No data

Zamorano et al., 2019; Reiche, 1843b

Peruphorticus rugatus (Reiche, 1843)*

No data

Zamorano et al., 2019; Reiche, 1843b

Peruphorticus rugosus (Dejean, 1831)*

BOL

Zamorano et al., 2019

Stenocheila Laporte de Castelnau, 1832

Stenocheila lacordairei Laporte de Castelnau, 1832

MET

Martínez, 2003

Lebiini Bonelli, 1810

Agra Fabricius, 1801

Agra aculeata Chaudoir, 1854*

No data

Chaudoir, 1854

Agra amoena Chaudoir, 1861*

No data

Chaudoir, 1861

Agra ardoini Straneo, 1982*

CUN

Straneo, 1982

Agra aurora Liebke, 1940*

No data

Liebke, 1940

Agra azurea Chaudoir, 1861*

No data

Chaudoir, 1861

Agra baleni Steinheil, 1875*

BOY

Steinheil, 1875a

Agra barrensis Straneo, 1955

No data

Erwin, 2002

Agra bogotana Straneo, 1979*

CUN

Straneo, 1982

Agra castaneipes Bates, 1883

No data

Erwin, 2002

Agra cauca Erwin, 1998*

CAU

Erwin, 1998

Agra cribricollis Chaudoir, 1861*

No data

Chaudoir, 1861

Agra cyaneucnemes Erwin, 1984*

MAG

Erwin, 1984

Agra denticulata Steinheil, 1875*

ANT

Steinheil, 1875a

Agra dorazul Erwin, 1984*

SAN

Erwin, 1984

Agra eowilsoni Erwin, 1998*

VAC

Erwin, 1998

Agra incisa Liebke, 1938

MAG

Erwin, 2002

Agra jedlickai Liebke, 1938*

No data

Liebke, 1938

Agra macra Steinheil, 1875*

ANT

Steinheil, 1875a

Agra magdalena Erwin, 1987*

SAN

Erwin, 1987

Agra mauritii Straneo, 1982*

CUN

Straneo, 1982

Agra multifoveolata Steinheil, 1875*

ANT

Steinheil, 1875a

Agra nova Straneo, 1982*

CUN

Straneo, 1982

Agra pallipes Liebke, 1938*

No data

Liebke, 1938

Agra palmata Steinheil, 1875*

ANT, BOY, SAN

Steinheil, 1875a; Erwin, 1984

Agra pehlkei Liebke, 1938*

SAN, TOL

Erwin, 1987

Agra perrinae Straneo, 1982*

CUN

Straneo, 1982

Agra piligera Straneo, 1982*

CUN

Straneo, 1982

Agra proxima Straneo, 1982*

CUN

Straneo, 1982

Agra setifemoris Straneo, 1982*

No data

Straneo, 1982

Agra sexdentata Straneo, 1982*

VAC

Straneo, 1982

Agra smaragdinipennis (Steinheil, 1875)*

MAG

Erwin, 1983; Steinheil, 1875a

Agra sparsepunctata Straneo, 1982*

CUN

Straneo, 1982

Agra spinosa Liebke, 1940*

No data

Liebke, 1940; Mroczkowski, 1960

Agra strangulata Chaudoir, 1863

VAC, CUN

Erwin, 1991; Erwin, 2002

Agra subtilicornis Straneo, 1982*

CUN

Straneo, 1982

Agra tetraspina Straneo, 1982*

CUN

Straneo, 1982

Agra variabilis Straneo, 1982*

CUN

Straneo, 1982

Apenes LeConte, 1851

Apenes (Apenes) aerea Steinheil, 1875*

CUN

Steinheil, 1875a

Apenes (Apenes) cayennensis (Buquet, 1835)

No data

Motschulsky, 1864

Apenes (Apenes) maculata (Gory, 1833)

No data

Reiche, 1842b

Apenes (Apenes) mazoreoides Chaudoir, 1875*

No data

Chaudoir, 1875

Apenes (Apenes) quadripunctata (Reiche, 1842)*

No data

Reiche, 1842b

Apenes (Apenes) steinheili Ball & Shpeley, 1992*

TOL

Ball & Shpeley, 1992

Apenes (Apenes) stigmata Liebke, 1939*

No data

Mroczkowski, 1960

Apenes (Didymochaeta) postica (Dejean, 1831)*

BOL

Chaudoir, 1875

Axinopalpus LeConte, 1846

Axinopalpus pusillus (Dejean, 1831)

BOL

Dejean, 1831

Calleida Latreille, 1824

Calleida (Calleida) amethystina (Fabricius, 1787)

VAC

Arenas-Clavijo & Posso-Gómez, 2017

Calleida (Calleida) bicolor Reiche, 1842

No data

Reiche, 1842b

Calleida (Calleida) bogotana Liebke, 1935*

CUN

Mroczkowski, 1960

Calleida (Calleida) chevrolati Chaudoir, 1873*

No data

Chaudoir, 1873

Calleida (Calleida) conica Reiche, 1842*

No data

Reiche, 1842c

Calleida (Calleida) cuprea Chaudoir, 1873*

No data

Chaudoir, 1873

Calleida (Calleida) flava Chevrolat, 1833

No data

Reiche, 1842c; Bates, 1883

Calleida (Calleida) fulvipes Reiche, 1842*

VAC

Reiche, 1842c; Arenas-Clavijo & Posso-Gómez, 2017

Calleida (Calleida) janthina Reiche, 1842*

No data

Reiche, 1842c

Calleida (Calleida) koppeli Steinheil, 1875*

BOY

Steinheil, 1875a

Calleida (Calleida) lindigi Chaudoir, 1873*

No data

Chaudoir, 1873

Calleida (Calleida) lurida Chaudoir, 1873*

No data

Chaudoir, 1873

Calleida (Calleida) ohausi Liebke, 1939

VAC

Arenas-Clavijo & Posso-Gómez, 2017

Calleida (Calleida) onorei Casale, 2008

VAC

Arenas-Clavijo & Posso-Gómez, 2017

Calleida (Calleida) pallida Reiche, 1842*

No data

Reiche, 1842c

Calleida (Calleida) resplendens Reiche, 1842*

CUN

Reiche, 1842b

Calleida (Calleida) rutilans Chaudoir, 1850*

VAC

Chaudoir, 1850; Arenas-Clavijo & Posso-Gómez, 2017

Calleida (Calleida) sanguinicollis Dejean, 1831

BOL

Dejean, 1831

Calleida (Calleida) schumacheri Steinheil, 1875

ANT, VAC

Arenas-Clavijo & Posso-Gómez, 2017; Steinheil 1875a

Calleida (Calleida) similis Reiche, 1842

No data

Reiche, 1842c; Bates, 1883

Calleida (Calleida) smaragdinipennis Reiche, 1842*

No data

Reiche, 1842b

Calleida (Calleida) smaragdula Reiche, 1843*

No data

Reiche, 1842c

Calleida (Calleida) suturella Reiche, 1842

No data

Reiche, 1842b; Chaudoir, 1852

Calleida (Calleida) tibialis Brullé, 1837

No data

Chaudoir, 1873

Calleida (Calleida) viridana Liebke, 1939*

No data

Mroczkowski, 1960

Calleida (Callidiola) aurata Motschulsky, 1864

No data

Bates, 1883

Callidadelpha Steinheil, 1875

Callidadelpha bogotana Steinheil, 1875*

CUN

Steinheil, 1875a

Carbonellia Mateu, 1968

Carbonellia (Pseudocarbonellia) atra (Mateu, 1972)

NSA

Mateu, 1972

Coptodera Dejean, 1825

Coptodera (Coptodera) acutipennis (Buquet, 1835)

MAG

Shpeley & Ball, 1993

Coptodera (Coptodera) aeneorufa Bates, 1869

AMA

Martínez, 2003

Coptodera (Coptodera) apicalis Shpeley & Ball, 1993

VAC

Shpeley & Ball, 1993

Coptodera (Coptodera) chalcites Bates, 1869

AMA

Shpeley & Ball, 1993; Martínez, 2003

Coptodera (Coptodera) championi Bates, 1883

VAC

Shpeley & Ball, 1993

Coptodera (Coptodera) festiva Dejean, 1825

MAG

Martínez, 2003

Coptodera (Coptodera) megalops Bates, 1869

CAQ

Shpeley & Ball, 1993

Coptodera (Coptodera) nigrostriata (Reiche, 1843)

MAG

Shpeley & Ball, 1993

Coptodera (Coptodera) nitidula (Buquet, 1835)

No data

Shpeley & Ball, 1993

Coptodera (Coptodera) picea Dejean, 1826

TOL

Shpeley & Ball, 1993

Coptodera (Coptodera) relucens Bates, 1869

AMA

Martínez, 2003

Coptodera (Coptodera) schaumii Chaudoir, 1861

CHO, SAN, BOY, CAL, VAC

Shpeley & Ball, 1993

Coptodera (Coptodera) transversa (Reiche, 1843)

No data

Reiche, 1843d; Shpeley & Ball, 1993

Coptodera (Coptodera) undulata Perty, 1830

No data

Shpeley & Ball, 1993

Coptodera (Coptodera) versicolor Bates, 1869

AMA

Shpeley & Ball, 1993

Cryptobatis Eschscholtz, 1829

Cryptobatis janthoptera (Reiche, 1842)

No data

Reiche, 1842c; Bates, 1883

Cylindronotum Putzeys, 1845

Cylindronotum nevermanni (Liebke, 1930)

MET

Erwin, 2004

Dromius Bonelli, 1810

Dromius (Dromius) bordoni Mateu, 1979*

CUN

Mateu, 1991

Dromius (Dromius) martae Mateu, 1991*

MAG

Mateu, 1991

Dromius bohumilae Mateu, 1982*

No data

Mateu, 1991

Dromius columbianus Mateu, 1973*

No data

Mateu, 1991

Eucheila Dejean, 1829

Eucheila (Inna) boyeri (Solier, 1835)

MAG

Shpeley & Ball, 2000

Eucheila (Inna) costulata (Chaudoir, 1872)

No data

Shpeley & Ball, 2000

Euphorticus laevicollis (Reiche, 1843)

No data

Zamorano et al., 2019

Euplatia Chaudoir, 1872

Euplatia columbica Steinheil, 1875*

ANT

Steinheil, 1875a

Euproctinus Leng & Mutchler, 1927

Euproctinus (Neoeuproctus) columbianus Shpeley, 1986*

No data

Shpeley, 1986

Euproctinus (Neoeuproctus) howdeni Shpeley, 1986*

VAC

Shpeley, 1986

Euproctinus (Neoeuproctus) puzteysi (Chaudoir, 1873)*

CUN

Shpeley, 1986

Euproctinus (Neoeuproctus) quadriplagiatus (Reiche, 1842)

No data

Reiche, 1842c; Shpeley, 1986

Eurycoleus Chaudoir, 1848

Eurycoleus fofus Reichardt, 1976

AMA

Shpeley & Ball, 2000

Eurycoleus macularius (Chevrolat, 1835)

CES, CUN, BOY, VAC

Shpeley & Ball, 2000; Ruiz-Tapiador & Arenas, 2015

Hyboptera Chaudoir, 1873

Hyboptera angulicollis Chaudoir, 1873

AMA, CAQ, NAR

Erwin & Henry, 2017; Martínez, 2003

Hyboptera auxiliadora Erwin, 2004

BOL

Sarmiento-Roa et al., 2020

Hyboptera tiputini Erwin & Henry, 2017

AMA, CHO, VAC

Erwin & Henry, 2017

Hyboptera tuberculata (Dejean, 1825)

AMA

Erwin & Henry, 2017; Martínez, 2003

Hyboptera verrucosa (Reiche, 1842)

AMA

Erwin & Henry, 2017

Lebia Latreille, 1802

Lebia (Chelonodema) championi (Bates, 1883)

CUN

Reichardt, 1972

Lebia (Chelonodema) erotyloides Reichardt, 1972

COR

Martínez, 2003

Lebia (Chelonodema) howdeni Reichardt, 1972*

VAC

Reichardt, 1972

Lebia (Chelonodema) ocelligera (Bates, 1883)

CUN, BOY

Reichardt, 1972

Lebia (Lebia) amabilis (Chaudoir, 1871)

No data

Bates, 1883

Lebia (Lebia) amoenula (Chaudoir, 1871)

No data

Chaudoir, 1871

Lebia (Lebia) angulata Dejean, 1831

BOL

Dejean, 1831

Lebia (Lebia) atricapillus Liebke, 1931*

SAN

Putzeys, 1878b

Lebia (Lebia) bitaeniata Chevrolat, 1834

AMA, VAC

Martínez, 2003

Lebia (Lebia) brachinoides Reiche, 1842

No data

Reiche, 1842c; Bates, 1883

Lebia (Lebia) callida Liebke, 1938*

No data

Mroczkowski, 1960

Lebia (Lebia) cannae Steinheil, 1875*

CAL, CAQ, VID

Steinheil 1875a

Lebia (Lebia) chlorotica Dejean, 1831

No data

Bates 1883,

Lebia (Lebia) cognata Chaudoir, 1871*

No data

Chaudoir, 1871

Lebia (Lebia) confusula Chaudoir, 1871*

BOL

Chaudoir, 1871

Lebia (Lebia) contigua Chaudoir, 1871*

No data

Chaudoir, 1871

Lebia (Lebia) dentata Chaudoir, 1871*

PUT

Chaudoir, 1870

Lebia (Lebia) discernenda Chaudoir, 1871*

No data

Chaudoir, 1870

Lebia (Lebia) goudoti (Chaudoir, 1871)*

No data

Chaudoir, 1871

Lebia (Lebia) gratiosa (Chaudoir, 1871)*

No data

Chaudoir, 1871

Lebia (Lebia) haplomera Chaudoir, 1871*

No data

Chaudoir, 1871

Lebia (Lebia) lacerata Chaudoir, 1871*

No data

Chaudoir, 1870

Lebia (Lebia) leptodera (Chaudoir, 1871)*

No data

Chaudoir, 1871

Lebia (Lebia) longiloba Chaudoir, 1871*

BOL

Bates, 1883; Chaudoir, 1871

Lebia (Lebia) melanoptera Chaudoir, 1871*

No data

Chaudoir, 1871

Lebia (Lebia) mirabilis Bates, 1883

CAQ

Martínez, 2003

Lebia (Lebia) myops Dejean, 1831*

BOL

Chaudoir, 1871

Lebia (Lebia) nigrolineata Reiche, 1842*

BOL

Reiche, 1842c

Lebia (Lebia) nigromaculata Gory, 1833

BOL

Chaudoir, 1870

Lebia (Lebia) pallipes Gory, 1833

No data

Reiche, 1842c

Lebia (Lebia) picta (Steinheil, 1875)*

BOY

Steinheil, 1875a

Lebia (Lebia) puella Dejean, 1831*

BOL

Chaudoir, 1870

Lebia (Lebia) reflexicollis Chaudoir, 1843

No data

Chaudoir, 1871

Lebia (Lebia) ruficeps (Chaudoir, 1871)*

No data

Chaudoir, 1871

Lebia (Lebia) rugifrons Dejean, 1831*

BOL

Chaudoir, 1870

Lebia (Lebia) smaragdinipennis Reiche, 1842*

No data

Reiche, 1842c

Lebia (Lebia) subtilis (Chaudoir, 1871)

No data

Chaudoir, 1871

Lebia (Lebia) terminalis Putzeys, 1846

No data

Chaudoir, 1871

Lebia (Lebia) variegata Dejean, 1831*

BOL

Dejean, 1831

Lebia (Lebia) vicina (Chaudoir, 1871)

MAG

Chaudoir, 1871; Bates, 1883

Lebia argutula (Chaudoir, 1871)*

No data

Chaudoir, 1871

Lebia disconotata (Chaudoir, 1871)*

BOL

Chaudoir, 1871

Lebia distinguenda Putzeys, 1846

No data

Chaudoir, 1870

Lebia heydenii Putzeys, 1845*

No data

Chaudoir, 1870

Lebia limbata Steinheil, 1875*

QUI

Steinheil, 1875a

Lelis Chaudoir, 1869

Lelis quadrisignata (Buquet, 1835)

AMA

Shpeley & Ball, 2000

Lelis rutila (Bates, 1869)

BOY

Shpeley & Ball, 2000; Steinheil, 1875a

Mochtherus Schmidt-Göbel, 1846

Mochtherus tetraspilotus (MacLeay, 1825)

VAC

Torres-Dominguez et al., 2020

Negrea Mateu, 1968

Negrea opaca Mateu, 1982

MAG

Martínez, 2003

Negrea scutellaris (Dejean, 1834)

BOL

Mateu, 1982a

Nemotarsus LeConte, 1853

Nemotarsus fallax (Dejean, 1831)

BOL

Bates, 1883

Onota Chaudoir, 1873

Onota angulicollis (Reiche, 1842)

No data

Reiche, 1842c; Erwin, 2004

Onota rutilans Chaudoir, 1873

AMA

Martínez, 2003

Phloeoxena Chaudoir, 1870

Phloeoxena (Phloeoxena) biundata Steinheil, 1875*

NSA

Shpeley & Ball, 2000; Steinheil, 1875b

Phloeoxena (Oenaphelox) signata Dejean, 1825

No data

Chaudoir, 1870

Plochionus Dejean, 1821

Plochionus (Menidius) faviger Chaudoir, 1873*

No data

Chaudoir, 1873

Plochionus (Menidius) pictipennis (Reiche, 1842)*

VID

Reiche, 1842c

Plochionus (Menidius) pictus Chaudoir, 1873*

No data

Chaudoir, 1873

Plochionus (Plochionus) pallens (Fabricius, 1775)

No data

Bates, 1883; Chaudoir, 1872

Pseudotoglossa Mateu, 1961

Pseudotoglossa inaequalis (Chaudoir, 1873)

AMA

Martínez, 2003

Pseudotoglossa obscurella (Bates, 1878)

MAG

Erwin, 2004; Mateu, 1961

Pseudotoglossa terminalis (Chaudoir, 1873)

No data

Erwin, 2004; Mateu 1961

Stenognathus Chaudoir, 1843

Stenognathus (Gnathostenus) dentifemoratus Shpeley & Ball, 2000*

No data

Shpeley & Ball, 2000

Stenognathus (Pristolomus) dentifer (Chaudoir, 1870)

No data

Shpeley & Ball, 2000

Stenognathus (Stenognathus) crenulatus Chaudoir, 1870

CUN, PUT, VAC

Shpeley & Ball, 2000

Stenognathus (Stenognathus) longipennis Chaudoir, 1877*

BOY, VAC

Shpeley & Ball, 2000

Stenognathus (Stenognathus) platypterus Chaudoir, 1870

AMA

Shpeley & Ball, 2000

Stenognathus (Stenognathus) procerus (Putzeys, 1878)*

ANT

Putzeys, 1878b; Shpeley & Ball, 2000

Thoasia Liebke, 1939

Thoasia rugifrons Liebke, 1939

MAG

Reichardt, 1968

Morionini Brullé, 1834

Morion Latreille, 1810

Morion cordatus Chaudoir, 1837

AMA, CES, CHO, NAR

Reiche, 1843a; Martínez, 2003

Morion cyclomus Chaudoir, 1854

No data

Chaudoir, 1854

Morion monilicornis (Latreille, 1805)

No data

Chaudoir, 1854; Bates, 1883

Morion simplex Dejean, 1826

MAG

Martínez, 2003

Moriosomus Motschulsky, 1855

Moriosomus seticollis Straneo, 1985

No data

Erwin & Moore, 2007

Odacanthini Laporte de Castelnau, 1834

Calophaena Klug, 1821

Calophaena acuminata (Olivier, 1790)

No data

Reiche, 1842a

Calophaena arcuata (Guérin-Méneville, 1844)

No data

Bates, 1883

Calophaena bicincta (Dejean & Boisduval, 1829)

No data

Motschulsky, 1864

Calophaena cincta (Gray, 1832)

No data

Steinheil, 1875a

Calophaena grandispina Liebke, 1930

No data

Mroczkowski, 1960

Calophaena laevigata Bates, 1878

CHO

Martínez, 2003

Calophaena lafertei Guérin-Méneville, 1844*

No data

Guérin-Méneville, 1844

Calophaena unifasciata Chaudoir, 1861

No data

Chaudoir, 1861

Calophaena virgata Liebke, 1938*

No data

Mroczkowski, 1960

Colliuris DeGeer, 1774

Colliuris (Apiodera) funckii (Putzeys, 1845)

VID

Martínez, 2003

Colliuris (Apiodera) rugicollis (Dejean, 1825)

No data

Chaudoir, 1863

Colliuris (Apiodera) subdistincta (Chaudoir, 1863)

AMA

Martínez, 2003

Colliuris (Apioderella) rudis (Chaudoir, 1872)

RIS

Martínez, 2003

Colliuris (Colliurella) amoena (Chaudoir, 1863)*

No data

Chaudoir, 1863

Colliuris (Colliurita) variolosa (Chaudoir, 1863)*

No data

Chaudoir, 1863

Colliuris (Mimocasnonia) fusca (Reiche, 1842)

No data

Reiche, 1842a

Colliuris (Plagiorhytis) corrusca (Chaudoir, 1863)

No data

Chaudoir, 1863

Colliuris (Plagiorhytis) plicaticollis (Reiche, 1842)

No data

Reiche, 1842a

Colliuris (Pseudocasnonia) viridicollis (Chaudoir, 1863)

No data

Chaudoir, 1863

Colliuris tetrastigma (Chaudoir, 1863)

AMA

Martínez, 2003

Oodinus Motschulsky, 1864

Oodinus alutaceus (Bates, 1882)

AMA

Martínez, 2003

Pentagonica Shmidt-Göbel, 1846

Pentagonica flavipes (LeConte, 1853)

AMA, MAG, NAR

Reichardt, 1968; Martínez, 2003

Pentagonica maculicornis Bates, 1883

MAG

Reichardt, 1968

Pentagonica ochracea Reichardt, 1968

VID

Martínez, 2003

Pentagonica roedingeri Liebke, 1951

AMA

Martínez, 2003

Pentagonica scutellaris Chaudoir, 1877

AMA

Martínez, 2003

Pentagonica trivittata (Dejean, 1831)

BOL

Dejean, 1831

Stenocrepis Chaudoir, 1857

Stenocrepis (Stenocrepis) pauper Chaudoir, 1857

No data

Chaudoir, 1857

Stenocrepis (Stenous) fuscipes (Laferté-Sénectère, 1851)

No data

Laferté-Sénectère, 1851

Stenocrepis (Stenous) gilvipes (Laferté-Sénectère, 1851)

No data

Reiche, 1843b; Chaudoir, 1857

Stenocrepis (Stenous) metallica (Dejean, 1826)

No data

Chaudoir; 1857

Stenocrepis (Stenous) tibialis (Chevrolat, 1834)

No data

Laferté-Sénectère, 1851

Stenocrepis aeruginea (Laferté-Sénectère, 1851)

No data

Laferté-Sénectère, 1851

Stenocrepis flavicrus (Laferté-Sénectère, 1851)*

No data

Laferté-Sénectère, 1851

Peleciini Chaudoir, 1880

Pelecium Kirby, 1819

Pelecium (Pelecidium) sulcatum Guérin-Méneville, 1843*

MAG, NSA, VAC

Straneo & Ball, 1989

Pelecium laevigatum Guérin-Méneville, 1843*

TOL

Straneo & Ball, 1989

Perigonini Horn, 1881

Mizotrechus Bates, 1872

Mizotrechus gorgona Erwin, 2011*

CAU

Erwin, 2011

Perigona Laporte de Castelnau, 1835

Perigona (Perigona) columbiana Putzeys, 1878*

BOY

Putzeys, 1878b

Platynini Bonelli, 1810

Dyscolus Dejean, 1831

Dyscolus (Dyscolidion) bracteatus (Moret, 1990)

CAU

Arenas-Clavijo & González, 2018

Dyscolus (Dyscolidion) cyanonotus Chaudoir, 1850

No data

Chaudoir, 1850; Martínez, 2003

Dyscolus (Dyscolidion) laticollis (Reiche, 1843)*

No data

Martínez & Ball, 2003

Dyscolus (Dyscolidion) leptomorphus (Chaudoir, 1879)*

CUN

Martínez & Ball, 2003

Dyscolus (Dyscolidion) politus (Putzeys, 1878)

CUN, ANT

Putzeys, 1878

Dyscolus (Dyscolidion) princeps (Bates, 1878)

No data

Martínez & Ball, 2003

Dyscolus (Dyscolidion) punctatostriatus (Putzeys, 1878)*

BOY, TOL

Martínez & Ball, 2003

Dyscolus (Dyscolidion) sinuosus (Chaudoir, 1878)*

No data

Martínez & Ball, 2003

Dyscolus (Dyscolidion) viridiauratus (Bates, 1878)

No data

Martínez & Ball, 2003

Dyscolus (Dyscolus) acutipennis Chaudoir, 1850*

No data

Martínez & Ball, 2003

Dyscolus (Dyscolus) acutus (Putzeys, 1878)*

NSA

Martínez & Ball, 2003

Dyscolus (Dyscolus) agonoides (Chaudoir, 1878)*

No data

Martínez & Ball, 2003

Dyscolus (Dyscolus) ahenonotus (Putzeys, 1878)*

CUN

Martínez & Ball, 2003

Dyscolus (Dyscolus) alpaeoides (Chaudoir, 1878)*

No data

Martínez & Ball, 2003

Dyscolus (Dyscolus) anthracinus (Putzeys, 1878)*

CUN

Martínez & Ball, 2003

Dyscolus (Dyscolus) asphaltinus (Chaudoir, 1878)

CUN

Martínez & Ball, 2003

Dyscolus (Dyscolus) atratus (Chaudoir, 1859)

MAG

Martínez & Ball, 2003

Dyscolus (Dyscolus) atroaeneus (Putzeys, 1878)*

BOY

Martínez & Ball, 2003; Perrault, 1990

Dyscolus (Dyscolus) beryllinus (Putzeys, 1878)*

CAL

Martínez & Ball, 2003

Dyscolus (Dyscolus) bispinosus (Chaudoir, 1878)*

No data

Martínez & Ball, 2003

Dyscolus (Dyscolus) bogotensis Perrault, 1992*

CUN

Martínez & Ball, 2003

Dyscolus (Dyscolus) brachypterus (Chaudoir, 1859)*

No data

Martínez & Ball, 2003

Dyscolus (Dyscolus) brevipennis (Motschulsky, 1865)*

No data

Martínez & Ball, 2003

Dyscolus (Dyscolus) brevis (Putzeys, 1878)*

No data

Martínez & Ball, 2003

Dyscolus (Dyscolus) carbonarius (Putzeys, 1878)*

CUN

Martínez & Ball, 2003

Dyscolus (Dyscolus) caucaensis Perrault, 1992*

VAC

Martínez & Ball, 2003

Dyscolus (Dyscolus) chalconotus (Chaudoir, 1878)*

CUN

Martínez & Ball, 2003

Dyscolus (Dyscolus) ciliatus (Chaudoir, 1878)*

CUN

Martínez & Ball, 2003

Dyscolus (Dyscolus) clarus (Chaudoir, 1878)*

BOY

Martínez & Ball, 2003

Dyscolus (Dyscolus) conicus (Chaudoir, 1879)

MAG

Martínez & Ball, 2003

Dyscolus (Dyscolus) consanguineus (Chaudoir, 1878)*

No data

Martínez & Ball, 2003

Dyscolus (Dyscolus) cordicollis (Motschulsky, 1865)

No data

Martínez & Ball, 2003

Dyscolus (Dyscolus) corvinus (Dejean, 1831)*

CUN

Martínez & Ball, 2003

Dyscolus (Dyscolus) cyaneocupreus (Putzeys, 1878)*

ANT, CAL, TOL

Chaudoir, 1878; Martínez & Ball, 2003

Dyscolus (Dyscolus) cyanicollis Brullé, 1834*

No data

Martínez & Ball, 2003

Dyscolus (Dyscolus) despiciendus (Chaudoir, 1878)*

No data

Martínez & Ball, 2003

Dyscolus (Dyscolus) donrwi Perrault, 1993*

BOY, CUN

Martínez & Ball, 2003

Dyscolus (Dyscolus) dyschromus (Chaudoir, 1878)*

No data

Martínez & Ball, 2003

Dyscolus (Dyscolus) feronioides (Reiche, 1843)*

ARA, BOY, CUN, MAG, MET, QUI, SAN, VAU

Martínez & Ball, 2003; Camero, 2003

Dyscolus (Dyscolus) grandicollis (Reiche, 1843)*

No data

Martínez & Ball, 2003

Dyscolus (Dyscolus) hexacoelus (Chaudoir, 1879)

No data

Chaudoir, 1879

Dyscolus (Dyscolus) inconspicuus (Chaudoir, 1878)*

CUN

Martínez & Ball, 2003

Dyscolus (Dyscolus) interruptus (Putzeys, 1878)*

ANT

Martínez & Ball, 2003

Dyscolus (Dyscolus) isabellae Camero, 2010*

MAG

Camero, 2010

Dyscolus (Dyscolus) kennedyensis Camero, 2010*

MAG

Camero, 2010

Dyscolus (Dyscolus) landolti (Putzeys, 1878)*

NSA, SAN

Martínez & Ball, 2003

Dyscolus (Dyscolus) latidens (Chaudoir, 1859)

No data

Martínez & Ball, 2003

Dyscolus (Dyscolus) longipennis (Reiche, 1843)*

No data

Martínez & Ball, 2003

Dyscolus (Dyscolus) lucidus (Chaudoir, 1879)*

BOL

Martínez & Ball, 2003

Dyscolus (Dyscolus) melas (Putzeys, 1878)*

SAN

Martínez & Ball, 2003

Dyscolus (Dyscolus) micans (Putzeys, 1878)*

BOL, SAN

Martínez & Ball, 2003

Dyscolus (Dyscolus) monterredonda Perrault, 1992*

CUN, HUI

Martínez & Ball, 2003

Dyscolus (Dyscolus) morosus (Chaudoir, 1878)*

No data

Martínez & Ball, 2003

Dyscolus (Dyscolus) muzo Perrault, 1993*

CUN

Martínez & Ball, 2003

Dyscolus (Dyscolus) obesulus (Chaudoir, 1878)*

MAG

Martínez & Ball, 2003

Dyscolus (Dyscolus) oopterus (Chaudoir, 1859)*

No data

Martínez & Ball, 2003

Dyscolus (Dyscolus) ovatus (Putzeys, 1878)*

BOY

Martínez & Ball, 2003

Dyscolus (Dyscolus) phaeocnemis (Chaudoir, 1879)*

No data

Martínez & Ball, 2003

Dyscolus (Dyscolus) physopterus (Chaudoir, 1878)*

No data

Martínez & Ball, 2003

Dyscolus (Dyscolus) piceolus (Chaudoir, 1878)*

SAN

Martínez & Ball, 2003

Dyscolus (Dyscolus) platynoides (Chaudoir, 1878)*

ARA, BOY, CAL, CUN, MAG, MET, QUI, SAN, TOL

Martínez & Ball, 2003; Camero, 2003

Dyscolus (Dyscolus) protensus (Putzeys, 1878)*

CUN

Martínez & Ball, 2003

Dyscolus (Dyscolus) pseudoconicus Perrault, 1992*

No data

Martínez & Ball, 2003

Dyscolus (Dyscolus) purpuratus Reiche, 1843

ANT, CAL, RIS, VAC

Martínez & Ball, 2003

Dyscolus (Dyscolus) quadricollis (Chaudoir, 1859)*

No data

Martínez & Ball, 2003

Dyscolus (Dyscolus) reichei (Perrault, 1989)

No data

Martínez & Ball, 2003

Dyscolus (Dyscolus) rutilans (Motschulsky, 1865)

BOY

Martínez & Ball, 2003

Dyscolus (Dyscolus) seriepunctatus (Chaudoir, 1859)*

No data

Martínez & Ball, 2003

Dyscolus (Dyscolus) spinipennis (Reiche, 1843)*

No data

Martínez & Ball, 2003

Dyscolus (Dyscolus) steinheili Perrault, 1993*

ARA, BOY, CAL, CUN, MAG, MET, NSA, SAN, VAU

Martínez & Ball, 2003; Camero, 2003

Dyscolus (Dyscolus) striatulus (Chaudoir, 1878)*

No data

Martínez & Ball, 2003

Dyscolus (Dyscolus) subangulatus (Chaudoir, 1878)*

No data

Martínez & Ball, 2003

Dyscolus (Dyscolus) subiridescens (Chaudoir, 1878)*

No data

Martínez & Ball, 2003

Dyscolus (Dyscolus) subreflexus (Chaudoir, 1878)*

No data

Martínez & Ball, 2003

Dyscolus (Dyscolus) subviolaceus (Chaudoir, 1842)

RIS, SAN

Martínez & Ball, 2003

Dyscolus (Dyscolus) sulcatus (Guérin-Méneville, 1844)*

No data

Martínez & Ball, 2003

Dyscolus (Dyscolus) thiemei Perrault, 1990*

No data

Martínez & Ball, 2003

Dyscolus (Dyscolus) trapezicollis Chaudoir, 1878

CUN, NSA, SAN

Martínez & Ball, 2003; Perrault, 1990

Dyscolus (Dyscolus) unipunctatus Perrault, 1990*

CUN

Martínez & Ball, 2003

Dyscolus (Dyscolus) vegaensis Perrault, 1992*

CUN

Martínez & Ball, 2003

Dyscolus (Dyscolus) villavicencio Perrault, 1992*

MET

Martínez & Ball, 2003

Dyscolus (Glyptolenopsis) aeneipennis (Dejean, 1831)

BOL

Dejean, 1831

Dyscolus (Glyptolenopsis) degallieri (Perrault, 1991)

NAR

Martínez & Ball, 2003

Dyscolus (Stenocnemion) arenasi Moret, 2019*

VAC

Moret, 2019

Dyscolus (Stenocnemion) martinezae Moret, 2019*

VAC

Moret, 2019

Glyptolenoides Perrault, 1991

Glyptolenoides azureipennis (Chaudoir, 1859)

No data

Martínez & Ball, 2003

Glyptolenoides azureus (Chaudoir, 1859)

NSA

Martínez & Ball, 2003

Glyptolenoides cyclothorax (Chaudoir, 1879)

No data

Martínez & Ball, 2003

Glyptolenoides elegantulus (Chaudoir, 1878)*

No data

Martínez & Ball, 2003

Glyptolenoides purpuripennis (Chaudoir, 1879)

No data

Perrault, 1991

Glyptolenoides sulcipennis (Chaudoir, 1879)*

CUN

Martínez & Ball, 2003

Glyptolenoides sulcitarsis (Chaudoir, 1878)*

No data

Martínez & Ball, 2003

Glyptolenus Bates, 1878

Glyptolenus apicestriatus (Reiche, 1843)*

No data

Martínez & Ball, 2003

Glyptolenus chalybeus (Dejean, 1831)

ARA, BOY, CAL, CAU, CUN, MET, SAN, TOL, VAU

Camero, 2003; Arenas-Clavijo & González, 2018

Glyptolenus convexiusculus (Chaudoir, 1878)

No data

Chaudoir, 1878

Glyptolenus janthinus (Dejean, 1831)

No data

Martínez & Ball, 2003

Glyptolenus nigrita (Chaudoir, 1879)*

No data

Martínez & Ball, 2003

Glyptolenus nitidipennis (Chaudoir, 1850)*

No data

Martínez & Ball, 2003

Glyptolenus spinosus (Reiche, 1843)*

No data

Martínez & Ball, 2003

Incagonum Liebherr, 1994

Incagonum aeneum (Reiche, 1843)

BOY, CAU, HUI, CAL, CUN, QUI

Martínez & Ball, 2003

Incagonum pedestre (Putzeys, 1878)*

CUN

Martínez & Ball, 2003

Sericoda Kirby, 1837

Sericoda bembidioides Kirby, 1837

BOY, CUN, TOL

Martínez & Ball, 2003

Pterostichini Bonelli, 1810

Abaris Dejean, 1831

Abaris (Abaridius) retiaria Will, 2002

MAG

Will, 2002

Abaris (Abaris) aenea Dejean, 1831

BOL, MAG

Will, 2002

Abaris (Abaris) basistriata Chaudoir, 1874

MAG

Will, 2002

Blennidus Motschulsky, 1865

Blennidus aberrans (Straneo, 1985)*

MAG

Straneo, 1985

Blennidus angularis (Straneo, 1985)*

MAG

Straneo, 1985

Blennidus bistriatus (Straneo, 1951)*

MAG

Straneo, 1951

Blennidus darlingtoni (Straneo, 1951)*

MAG

Straneo, 1951

Blennidus davidsoni (Straneo, 1985)*

MAG

Straneo, 1985

Blennidus dianae Camero, 2006*

MAG

Camero, 2006

Blennidus kochalkai (Straneo, 1985)*

MAG

Straneo, 1985

Blennidus laevigatus (Straneo, 1951)*

MAG

Straneo, 1951

Blennidus laevis (Straneo, 1951)

MAG

Straneo, 1951

Blennidus minutus (Straneo, 1951)*

MAG

Straneo, 1951

Blennidus montanus (Straneo, 1951)*

MAG

Straneo, 1951

Blennidus parvulus (Straneo, 1951)*

MAG

Straneo, 1951

Blennidus smaragdinus (Straneo, 1951)*

MAG

Straneo, 1951

Blennidus striolatus (Straneo, 1951)*

MAG

Straneo, 1951

Blennidus subcordatus (Straneo, 1951)*

MAG

Straneo, 1951

Blennidus uniformis (Straneo, 1951)*

MAG

Straneo, 1951

Hybothecus Chaudoir, 1874

Hybothecus incrassatus Chaudoir, 1874*

No data

Chaudoir, 1874b

Hybothecus sculptilis (Putzeys, 1878)*

ANT

Putzeys, 1878b

Loxandrus LeConte, 1852

Loxandrus latifascia Straneo, 1991

No data

Straneo, 1991

Loxandrus minimus Straneo, 1951

MAG

Straneo, 1951

Loxandrus interruptus Tschitscherine, 1900*

TOL

Tschitschérine, 1900

Loxandrus opaculus Bates, 1871

CUN

Martínez, 2003

Loxandrus ornatus Putzeys, 1878*

CUN

Putzeys, 1878b; Straneo, 1991

Loxandrus pictoides Straneo, 1991

VAC

Straneo, 1991; Martínez, 2003

Loxandrus tetrastigma Bates, 1871

RIS, VAC

Arenas-Clavijo & Posso-Gómez, 2017

Oribazus Chaudoir, 1874

Oribazus catenulatus Chaudoir, 1874

No data

Chaudoir, 1874b

Oribazus quinquestriatus Chaudoir, 1874

No data

Chaudoir, 1874b

Oxycrepis

Oxycrepis leucocera Reiche, 1843

No data

Will, 2005

Pseudabarys

Pseudabarys lebasi (Chaudoir, 1874)*

No data

Chaudoir, 1874a

Stolonis Motschulsky, 1866

Stolonis elegans (Dejean, 1831)*

BOL

Chaudoir, 1873

Stolonis parvula (Straneo, 1951)*

MAG

Will, 2005

Sphodrini Laporte de Castelnau, 1834

Laemostenus Bonelli, 1810

Laemostenus (Laemostenus) complanatus (Dejean, 1828)

AMA, BOY, CAL, CUN, HUI, MET, NAR, NSA, RIS, SAN, TOL

Martínez & Ball, 2003

Zuphiini Bonelli, 1810

Pseudaptinus Laporte de Castelnau, 1834

Pseudaptinus (Thalpius) intermedius (Chaudoir, 1872)*

No data

Chaudoir, 1872

Zuphioides Ball & Shpeley, 2013

Zuphioides capitum (Liebke, 1933)*

No data

Liebke, 1933; Ball & Shpeley, 2013

Zuphioides columbianum (Chaudoir, 1872)*

No data

Chaudoir, 1872; Ball & Shpeley, 2013

Zuphioides exiguum (Putzeys, 1878)*

VAC

Putzeys, 1878b; Ball & Shpeley, 2013

Licininae Bonelli, 1810

Chlaeniini Brullé, 1834

Chlaenius Bonelli, 1810

Chlaenius (Chlaenius) fallax (Olivier, 1795)

No data

Chaudoir, 1873

Chlaenius (Chlaenius) leucoscelis Chevrolat, 1835

No data

Chaudoir, 1873

Chlaenius (Chlaenius) viridicollis Reiche, 1843

No data

Reiche, 1843b

Melaeninae Alluaud, 1934

Melaenini Csiki, 1933

Cymbionotum Baudi di Selve, 1864

Cymbionotum (Procoscinia) fernandezi Ball & Shpeley, 2005*

BOL

Ball & Shpeley, 2005

Paussinae Latreille, 1807

Ozaenini Hope, 1838

Ozaena Olivier, 1811

Ozaena dentipes Olivier, 1811

MET

Martínez, 2003

Ozaena martinezi Ogueta, 1965*

MET

Martínez, 2003

Pachyteles Perty, 1830

Pachyteles angustatus Chaudoir, 1868*

No data

Chaudoir, 1868a

Pachyteles baleni Steinheil, 1875*

ANT

Steinheil, 1875b

Pachyteles castaneus (Dejean, 1831)

BOL

Chaudoir, 1868a

Pachyteles gyllenhalii (Dejean, 1825)

No data

Chaudoir, 1852

Pachyteles haroldi Steinheil, 1875*

BOY

Steinheil, 1875b

Pachyteles politus (Reiche, 1843)*

No data

Reiche, 1843a; Chaudoir, 1854

Pachyteles seriepunctatus Chaudoir, 1868*

No data

Chaudoir, 1868

Pachyteles striola Perty, 1830

No data

Chaudoir, 1852

Physea Brullé, 1835

Physea testudinea (Klug, 1834)

BOY, MET

Martínez, 2003

Paussini Latreille, 1806

Homopterus Westwood, 1841

Homopterus cunctans Reichensperger, 1938

CAU

Arenas-Clavijo & González, 2018

Homopterus steinbachi Kolbe, 1920

BOY

Darlington, 1950

Homopterus subcordatus Darlington, 1950

CAQ

Sarmiento-Roa et al., 2020

Rhysodinae Laporte de Castelnau, 1840

Rhysodini Laporte de Castelnau, 1840

Clinidium Kirby, 1830

Clinidium (Clinidium) cavicolle Chevrolat, 1873

NSA

Bell & Bell, 1985

Clinidium (Clinidium) curvatum Bell & Bell, 1985*

NSA

Bell & Bell. 1985

Clinidium (Clinidium) granatense Chevrolat, 1873*

ANT, CUN, BOY

Bell & Bell, 1985; Bell & Bell, 2009

Clinidium (Clinidium) hammondi Bell & Bell, 1985*

CUN

Bell & Bell, 1985

Clinidium (Clinidium) humboldti Bell & Bell, 1985*

No data

Bell & Bell, 1985

Clinidium (Clinidium) humile Bell & Bell, 1985*

No data

Bell & Bell, 1985

Clinidium (Clinidium) integrum Grouvelle, 1903

AMA

Bell & Bell, 2009

Clinidium (Clinidium) kochalkai Bell & Bell, 1985*

MAG

Bell & Bell, 1985

Clinidium (Clinidium) mathani Grouvelle, 1903

CAQ, CAU

Bell & Bell, 2009; Martínez, 2003

Clinidium (Clinidium) oberthueri Grouvelle, 1903

NAR

Bell & Bell, 2009

Clinidium (Clinidium) penicillatum Bell & Bell, 1985*

VAC

Bell & Bell, 1985

Clinidium (Clinidium) spatulatum Bell & Bell, 1985

CAU

Bell & Bell, 2009; Martínez, 2003

Scaritinae Bonelli, 1810

Clivinini Rafinesque, 1815

Ardistomis Putzeys, 1846

Ardistomis dubia Putzeys, 1846

No data

Putzeys, 1846

Ardistomis dyschirioides Putzeys, 1846

No data

Putzeys, 1846

Ardistomis ovata Putzeys, 1846*

No data

Putzeys, 1846

Ardistomis seriepunctata (Brullé, 1843)

No data

Valdés, 2009

Aspidoglossa Putzeys, 1846

Aspidoglossa mexicana (Chaudoir, 1837)

No data

Putzeys, 1867

Aspidoglossa pallida Putzeys, 1846*

No data

Putzeys, 1846

Aspidoglossa rivalis Putzeys, 1846

No data

Putzeys, 1846

Aspidoglossa submetallica Putzeys, 1846

No data

Putzeys, 1846

Clivina Latreille,1802

Clivina (Clivina) erythropus Putzeys, 1846*

No data

Putzeys, 1846

Clivina (Clivina) lebasii Putzeys, 1846*

No data

Putzeys, 1846

Clivina (Clivina) quadrata Putzeys, 1867*

BOL

Putzeys, 1867

Clivina (Paraclivina) fasciata Putzeys, 1846

No data

Putzeys, 1846

Clivina (Paraclivina) fuscipes Putzeys, 1846*

No data

Putzeys, 1846

Clivina (Paraclivina) tristis Putzeys, 1846*

No data

Putzeys, 1846

Clivina (Paraclivina) tuberculata Putzeys, 1846*

CUN

Putzeys, 1846

Clivina (Semiclivina) armata Putzeys, 1846*

BOL

Putzeys, 1846

Clivina (Semiclivina) columbica Putzeys, 1846*

No data

Putzeys, 1846

Clivina (Semiclivina) dissimilis Putzeys, 1846*

No data

Putzeys, 1846

Clivina (Semiclivina) laticeps Putzeys, 1846*

No data

Putzeys, 1846

Clivina (Semiclivina) latimanus Putzeys, 1846*

No data

Putzeys, 1846

Clivina (Semiclivina) oblita Putzeys, 1867*

No data

Putzeys, 1867

Cryptomma Putzeys, 1846

Cryptomma multistriatum Putzeys, 1846*

No data

Putzeys, 1846

Oxydrepanus Putzeys, 1867

Oxydrepanus ovalis Putzeys, 1867*

No data

Putzeys, 1867

Pyramis Putzeys, 1846

Pyramis crassicornis Putzeys, 1846*

No data

Putzeys, 1846

Schizogenius Putzeys, 1846

Schizogenius (Genioschizus) impressicollis Putzeys, 1846*

No data

Whitehead, 1972; Putzeys, 1846

Schizogenius (Genioschizus) impuncticollis Whitehead, 1972*

MAG

Whitehead, 1972

Schizogenius (Genioschizus) suturalis Whitehead, 1972*

MAG

Whitehead, 1972

Schizogenius (Genioschizus) szekessyi Kult, 1950

MAG

Whitehead, 1972

Schizogenius (Genioschizus) tenuis Bates, 1881

MAG, TOL

Whitehead, 1972

Schizogenius (Listropus) dyschirioides Putzeys, 1861

MAG

Whitehead, 1972

Schizogenius (Schizogenius) capitalis Putzeys, 1861*

ANT

Whitehead, 1972

Schizogenius (Schizogenius) darlingtoni Kult, 1950

No data

Whitehead, 1972

Schizogenius (Schizogenius) gracilis Putzeys, 1846

No data

Putzeys, 1846

Schizogenius (Schizogenius) interstriatus Putzeys, 1878*

ANT

Putzeys, 1878b

Schizogenius (Schizogenius) pygmaeus Van Dyke, 1925

MAG

Whitehead, 1972

Schizogenius (Schizogenius) riparius Putzeys, 1878*

TOL

Putzeys, 1878b

Schizogenius (Schizogenius) strigicollis Putzeys, 1846*

MAG

Whitehead, 1972; Putzeys, 1846

Schizogenius (Schizogenius) sulcatulus Putzeys, 1846*

No data

Putzeys, 1846

Semiardistomis Kult, 1950

Semiardistomis cordicollis (Putzeys, 1846)*

No data

Valdés, 2012

Semiardistomis pallipes (Dejean, 1831)

BOL

Dejean, 1831; Valdés, 2012

Forcipatorini Bänninger, 1937

Camptodontus Dejean, 1826

Camptodontus falcatus Putzeys, 1861*

No data

Putzeys, 1867

Camptodontus reichei Putzeys, 1861*

No data

Putzeys, 1867

Forcipator Maindron, 1904

Forcipator putzeysii (Chaudoir, 1868)*

No data

Chaudoir, 1868b

Stratiotes Putzeys, 1846

Stratiotes batesi Putzeys, 1867

NAR

Martínez, 2003

Scaritini Bonelli, 1810

Distichus Motschulsky, 1858

Distichus (Lophogenius) orientalis (Bonelli, 1813)

No data

Bänninger, 1938

Distichus (Lophogenius) lacordairei (Dejean, 1831)

No data

Bänninger, 1938

Glyptogrus Bates, 1881

Glyptogrus molopinus (Perty, 1830)

No data

Chaudoir, 1879

Scarites Fabricius, 1775

Scarites (Scarites) heterogrammus Perty, 1830

No data

Bänninger, 1938

Scarites (Scarites) illustris Chaudoir, 1880

No data

Bänninger, 1938

Scarites (Scarites) zambo Steinheil, 1875*

No data

Steinheil, 1875b; Bänninger, 1938

Taeniolobus Chaudoir, 1855

Taeniolobus (Taeniolobus) gratus (Chaudoir, 1855)*

No data

Chaudoir, 1880; Bänninger, 1938

Taeniolobus (Taeniolobus) guerini (Chaudoir, 1855)

No data

Chaudoir, 1855; Bänninger, 1938

Taeniolobus (Taeniolobus) oberthueri Bänninger, 1938*

ANT

Steinheil, 1875b; Bänninger, 1938

Taeniolobus (Taeniolobus) thiemei (Bänninger, 1933)*

No data

Bänninger, 1938

Taeniolobus (Taeniolobus) lebasii (Chaudoir, 1855)*

No data

Chaudoir, 1855; Bänninger, 1938

Siagoninae Bonelli, 1813

Siagonini Bonelli, 1813

Enceladus Bonelli, 1813

Enceladus gygas Bonelli, 1813

LAG

Arenas-Clavijo & Posso-Gómez, 2017

Trechinae Bonelli, 1810

Bembidiini Stephens, 1827

Bembidion Latreille, 1802

Bembidion (Antiperyphanes) angulicolle (Putzeys, 1878)*

CUN

Putzeys, 1878b

Bembidion (Ecuadion) boyaca Toledano, 2008*

BOY

Toledano, 2008

Bembidion (Ecuadion) chimborazonum Bates, 1871

VAC

Sarmiento-Roa et al., 2020

Bembidion (Ecuadion) cocuyanum Toledano, 2008*

BOY

Toledano, 2008

Bembidion (Ecuadion) colombianum Toledano, 2008*

CUN

Toledano, 2008

Bembidion (Ecuadion) putzeysii Csiki, 1928*

CUN

Putzeys, 1878b

Bembidion (Ecuadion) quebrada Toledano, 2008*

TOL

Toledano, 2008

Bembidion (Ecuadion) sanctaemarthae Darlington, 1934

MAG

Toledano, 2008

Bembidion (Ecuadion) subapterum Darlington, 1934

MAG

Toledano, 2008

Bembidion (Notaphus) basiplagiatum (Putzeys, 1878)

CUN

Putzeys, 1878b

Bembidion (Notaphus) cayambense Bates, 1891

CUN

Toledano, 2008

Bembidion (Notaphus) commissum Erichson, 1847

VAC

Toledano, 2008

Elaphropus Motschulsky, 1839

Elaphropus (Ammotachys) marchantarius Boyd & Erwin, 2016

AMA

Boyd & Erwin, 2016

Elaphropus (Nototachys) occidentalis Boyd & Erwin, 2016

AMA

Boyd & Erwin, 2016

Elaphropus (Tachyura) yunax (Darlington, 1939)

MAG

Martínez, 2003

Erwiniana Paulsen & Smith, 2003

Erwiniana alticola (Erwin, 1994)*

CUN

Erwin, 1994

Erwiniana anchicaya (Erwin, 1994)*

CAU, VAC

Erwin, 1994

Erwiniana depressisculptilis (Erwin, 1994)

AMA

Erwin, 1994

Erwiniana eugeneae (Erwin, 1994)

PUT

Erwin, 1994

Erwiniana hilaris (Bates, 1871)

AMA

Martínez, 2003

Erwiniana notparkeri (Erwin, 1994)*

PUT

Erwin, 1994

Erwiniana sculpticollis (Bates, 1871)

PUT

Erwin, 1994

Erwiniana sulcicostis (Bates, 1882)

CHO

Martínez, 2003

Erwiniana wygo (Erwin, 1994)*

CUN

Erwin, 1994

Gouleta Erwin, 1994

Gouleta cayennensis (Dejean, 1831)

ANT

Erwin, 1973

Gouleta gentryi Erwin, 1994

AMA

Martínez, 2003

Meotachys Erwin, 1974

Meotachys (Hylotachys) ballorum Boyd & Erwin, 2016

AMA

Boyd & Erwin, 2016

Meotachys (Scolistichus) riparius Boyd & Erwin, 2016

AMA

Boyd & Erwin, 2016

Pericompsus LeConte, 1852

Pericompsus (Eidocompsus) brasiliensis (Sahlberg, 1844)

MAG

Erwin, 1974

Pericompsus (Eidocompsus) immaculatus Bates, 1871

MAG

Erwin, 1974

Pericompsus (Pericompsus) concinnus (Laferté-Sénectère, 1841)

HUI

Erwin, 1974

Pericompsus (Pericompsus) diabalius Erwin, 1974*

MAG

Erwin, 1974

Pericompsus (Pericompsus) gracilior (Bates, 1884)

MAG

Erwin, 1974

Pericompsus (Pericompsus) histrionellus Bates, 1884

MAG

Erwin, 1974

Pericompsus (Pericompsus) reichei (Putzeys, 1845)

MAG

Erwin, 1974

Pericompsus (Pericompsus) silicis Erwin, 1974

CUN

Erwin, 1974

Pericompsus metallicus Bates, 1871

HUI

Erwin, 1974

Pogonini Laporte de Castelnau, 1834

Diplochaetus Chaudoir, 1872

Diplochaetus rutilus (Chevrolat, 1863)

LAG

Bousquet & Laplante, 1997; Reichardt, 1974a

Trechini Bonelli, 1810

Cnides Motschulsky, 1862

Cnides jeanneli Uéno, 1985

VAC

Jeannel, 1958

Cnides rostratus Motschulsky, 1862

TOL

Jeannel, 1958

Columbitrechus Mateu, 1982

Columbitrechus subsulcatus Mateu, 1982*

CAU

Mateu, 1982b

Oxytrechus Jeannel, 1927

Oxytrechus bousqueti Mateu, 1991*

CAU

Ruiz-Tapiador & Arenas, 2017

Oxytrechus campbelli Mateu, 1991*

CAU

Ruiz-Tapiador & Arenas, 2017

Oxytrechus caucaensis Mateu, 1991*

CAU

Ruiz-Tapiador & Arenas, 2017

Oxytrechus floresanus Giachino & Allegro, 2019*

CAL

Giachino et al., 2019

Oxytrechus jeanneli Mateu, 1991*

CAU

Ruiz-Tapiador & Arenas, 2017

Oxytrechus norae Mateu, 1982*

CAU

Ruiz-Tapiador & Arenas, 2017

Oxytrechus ruizianus Giachino & Allegro, 2019*

CAL

Giachino et al., 2019

Oxytrechus silvianus Mateu, 1991*

CAU

Ruiz-Tapiador & Arenas, 2017

Oxytrechus solitarius Mateu, 1991*

CAU

Ruiz-Tapiador & Arenas, 2017

Paratrechus Jeannel, 1920

Paratrechus incertus Mateu, 1999*

CAU

Mateu, 1998

Appendix 3. List of species of Cicindelidae Latreille, 1802 from Colombia until 2020, with their respective distribution within the country, species marked with asterisk (*) have been cited only from Colombia. Departments are codified according to ISO rule 3166-2. References are listed in appendix 1.

Tribe

Genus

Species

Department

References

Cicindelini Latreille, 1802

Brasiella Rivalier, 1954

Brasiella (Brasiella) argentata (Fabricius, 1801)

ANT, AMA, MET, PUT, VAC

Cassola & Pearson 2001, Ramírez-Mora 2008, Arenas-Clavijo 2018

Brasiella (Brasiella) mendicula Rivalier, 1955

ANT, MET, NAR, SAN, VAC

Cassola & Pearson 2001, Ramírez-Mora 2008, Arenas-Clavijo 2018

Brasiella (Brasiella) misella (Chaudoir, 1854)

ANT, BOL, CES, CUN, MAG, SAN, NAR, VAC.

Cassola & Pearson 2001, Ramírez-Mora 2008

Brasiella (Brasiella) nebulosa (Bates, 1874)

VAC

Cassola & Pearson 2001, Arenas-Clavijo 2018

Brasiella (Brasiella) venustula (Gory, 1833)

ANT, COR, MET, NSA, SAN, VAC

Cassola & Pearson 2001, Ramírez-Mora 2008, Arenas-Clavijo 2018

Callidema Guérin-Méneville, 1843

Callidema boussingaultii Guérin-Méneville, 1843

ANT, CAS, CAL, TOL, VAC

Cassola & Pearson 2001, Ramírez-Mora 2008

Cenothyla Rivalier, 1969

Cenothyla consobrina (Lucas, 1857)

AMA, MET

Cassola & Pearson 2001

Cenothyla klichai Moravec, 2015

MET

Moravec 2015

Cicindela Linnaeus, 1758

Cicindela (Cicindelidia) carthagena Dejean, 1831

BOL, CHO, VAC

Cassola & Pearson 2001, Vitolo & Pearson 2003, Arenas-Clavijo 2018

Cicindela (Cicindelidia) favergeri Audouin & Brullé, 1839

CUN, MET, PUT, VAC

Cassola & Pearson 2001, Arenas-Clavijo 2018

Cicindela (Cicindelidia) rufoaenea Horn, 1915

No data

Cassola & Pearson 2001

Cicindela (Cicindelidia) trifasciata Fabricius, 1781

No data

Cassola & Pearson 2001

Cylindera Westwood, 1831

Cylindera (Plectographa) suturalis (Fabricius, 1798)

No data

Cassola & Pearson 2001

Habroscelimorpha Dokhtouroff, 1883

Habroscelimorpha auraria (Klug, 1834)

LAG, MAG

Rodriguez et al. 1994, Vítolo & Pearson 2003, Ramírez-Mora 2008

Habroscelimorpha schwarzi (Horn, 1923)

VAC

Cassola & Pearson 2001, Arenas-Clavijo 2018

Langea Horn, 1901

Langea mellicollis Sumlin, 1993

AMA

Vítolo & Pearson 2003

Mesacanthina Rivalier, 1969

Mesacanthina chalceola (Bates, 1872)

MET

Moravec 2020

Odontocheila Laporte de Castelnau, 1834

Odontocheila angulipenis Horn, 1932

MET, VID

Cassola & Pearson 2001, Moravec 2013

Odontocheila batesii Chaudoir, 1860

AMA

Vítolo & Pearson 2003, Arenas-Clavijo 2018

Odontocheila bipunctata (Fabricius, 1792)

CAQ

Moravec 2016, Vítolo 2004

Odontocheila cajennensis (Fabricius, 1787)

No data

Moravec 2016

Odontocheila chrysis (Fabricius, 1801)

ANT, RIS

Vítolo & Pearson 2003

Odontocheila confusa (Dejean, 1825)

ANT, AMA, MET, PUT

Fernández et al 1993, Ramírez-Mora 2008

Odontocheila excisipenis Horn, 1932

ANT, CAU, CHO, NAR, VAC

Cassola & Pearson 2001, Moravec 2012, Arenas-Clavijo 2018

Odontocheila eximia Lucas, 1857

AMA, PUT

Vítolo & Pearson 2003

Odontocheila hamulipenis Horn, 1933*

VAC

Cassola & Pearson 2001, Moravec 2013, Arenas-Clavijo 2018

Odontocheila jordani Horn, 1898

CAU, NAR

Cassola & Pearson 2001, Torres-Dominguez & Mendivil-Nieto 2012

Odontocheila margineguttata (Dejean, 1825)

CAQ, GUA, GUV, MET

Cassola & Pearson 2001

Odontocheila ochreata (Reiche, 1842)

CAQ, MET, NAR, PUT

Moravec 2016, Vítolo 2004

Odontocheila oseryi (Lucas, 1857)

AMA, PUT

Moravec & Brzoska 2015, Vítolo 2004

Odontocheila salvini Bates, 1874

CHO, BOY, MAG

Vítolo & Pearson 2003, Steinheil 1875b

Odontocheila simulator Horn, 1894*

No data

Wiesner 1992, Vítolo & Pearson 2003

Odontocheila trilbyana Thomson, 1857

AMA, VAU

Vítolo & Pearson 2003

Opilidia Rivalier, 1954

Opilidia graphiptera (Dejean, 1831)

LAG, BOL, MAG

Cassola & Pearson 2001, Ramírez-Mora 2008

Opilidia macrocnema (Chaudoir, 1852)

CAU, NAR, VAC

Cassola & Pearson 2001, Arenas-Clavijo 2018

Oxygonia Mannerheim, 1837

Oxygonia albitaenia Bates, 1871

No data

Moravec 2015

Oxygonia fleutiauxi Horn, 1896

CAU

Kippenhan 1997

Oxygonia floridula Bates, 1872

No data

Vítolo & Pearson 2003

Oxygonia kippenhani Schüle, 2008*

BOY

Moravec 2017

Oxygonia kondratieffi Kippenhan, 1997

VAC

Kippenhan 1997, Moravec 2017, Arenas-Clavijo 2018

Oxygonia moreti Deuve, 1992

NAR, RIS, VAC

Kippenhan 1997, Moravec 2017, Arenas-Clavijo 2018

Oxygonia moronensis Bates, 1872

No data

Cassola & Pearson 2001

Oxygonia nigricans Horn, 1926

CAU

Kippenhan 1997, Moravec 2017

Oxygonia oberthueri Horn, 1896

ANT, NAR, RIS, VAC

Cassola & Pearson 2001, Ramírez-Mora 2008, Arenas-Clavijo 2018

Oxygonia prodiga (Erichson, 1847)

No data

Kippenhan 1997, Moravec 2015

Oxygonia schoenherrii Mannerheim, 1837

ANT, CUN, VAC

Kippenhan 1997, Moravec 2015

Oxygonia uniformis Horn, 1900

NAR

Vítolo & Pearson 2003

Oxygonia vuillefroyi Chaudoir, 1869

BOY, CUN, HUI

Vítolo & Pearson 2003

Pentacomia Bates, 1872

Pentacomia (Pentacomia) cupriventris (Reiche, 1842)

ANT, VAC

Cassola & Pearson 2001, Ramírez-Mora 2008, Arenas-Clavijo 2018

Pentacomia (Pentacomia) egregia (Chaudoir, 1835)

AMA

Cassola & Pearson 2001

Pentacomia (Poecilochila) lacordairei (Gory, 1833)

AMA, GUV

Cassola & Pearson 2001, Arenas-Clavijo 2018

Pentacomia (Poecilochila) ventralis (Dejean, 1825)

ANT, CES, MET, VID

Cassola & Pearson 2001, Ramírez-Mora 2008, Arenas-Clavijo 2018

Pentacomia chrysamma Bates, 1872

ANT

Cassola & Pearson 2001

Ronhuberia Moravec & Kudrna, 2002

Ronhuberia fernandezi (Cassola, 2000)

ANT

Moravec & Kudrna 2002

Ctenostomatini Laporte de Castelnau, 1834

Ctenostoma Klug, 1821

Ctenostoma (Ctenostoma) succinctum (Laporte, 1834)

GUV

Vítolo & Pearson 2003

Ctenostoma (Neoprocephalus) maculicorne (Chevrolat, 1856)

NAR, VAC

Vítolo & Pearson 2003, Arenas-Clavijo 2018

Ctenostoma (Procephalus) dormeri Horn, 1898

ANT, VAC

Naviaux 1998, Vítolo & Pearson 2003, Arenas-Clavijo 2018

Ctenostoma (Procephalus) ecuadorense Naviaux, 1998

CAU, VAC

Naviaux 1998, Vítolo & Pearson 2003, Arenas-Clavijo 2018

Ctenostoma (Procephalus) longipalpe Naviaux, 1998

No data

Naviaux 1998, Vítolo & Pearson 2003, Vítolo & Pearson 2003

Ctenostoma (Procephalus) maculosum Naviaux, 1998

CUN

Naviaux 1998, Vítolo & Pearson 2003, Vítolo & Pearson 2003

Ctenostoma (Procephalus) nigrum Chaudoir, 1860

PUT, VAC

Naviaux 1998, Vítolo & Pearson 2003, Vítolo & Pearson 2003

Ctenostoma (Procephalus) onorei Naviaux, 1998

CUN, VAC

Naviaux 1998, Vítolo & Pearson 2003, Arenas-Clavijo 2018

Megacephalini Laporte de Castelnau, 1834

Aniara Hope, 1838

Aniara sepulchralis (Fabricius, 1801)

CAQ, CAS, CUN, GUV, MET, TOL

Cassola & Pearson 2001, Vítolo & Pearson 2003

Metriocheila Thomson, 1857

Metriocheila nigricollis (Reiche, 1842)

HUI, PUT

Cassola & Pearson 2001, Vítolo & Pearson 2003

Phaeoxantha Chaudoir, 1850

Phaeoxantha aequinoctialis (Dejean, 1825)

CAS, MET

Fernandez et al 1993, Vítolo & Pearson 2003

Phaeoxantha klugii Chaudoir, 1850

CAU, MET, PUT

Fernandez et al 1993, Vítolo & Pearson 2003, Arenas-Clavijo 2018

Tetracha Hope, 1838

Tetracha (Neotetracha) affinis (Dejean, 1825)

AMA, ANT, ATL, BOL, BOY, CAL, CHO, CUN, GUV, HUI, MAG, MET, SAN, TOL, VAC

Wiesner 1992, Vítolo & Pearson 2003, Ramírez-Mora 2008

Tetracha (Neotetracha) cribrata Steinheil, 1875

ANT, BOL, CES, CUN, MET, NSA, SAN, TOL, VAC

Steinheil 1875a, Vitolo & Pearson 2003, Arenas-Clavijo 2018

Tetracha (Neotetracha) fulgida (Klug, 1834)

ANT, CAS, MET, PUT

Cassola & Pearson 2001, Vítolo & Pearson 2003, Ramírez-Mora 2008

Tetracha (Neotetracha) gracilis (Reiche, 1842)

No data

Reiche 1842a

Tetracha (Neotetracha) lacordairei (Gory, 1833)

ANT, BOY, CUN, HUI, MET, SAN

Cassola & Pearson 2001, Ramírez-Mora 2008

Tetracha (Tetracha) carolina (Linnaeus, 1763)

CAU, CES, RIS, VAC

Cassola & Pearson 2001, Vítolo & Pearson 2003

Tetracha (Tetracha) sobrina (Dejean, 1831)

AMA, ANT, BOL, BOY, CAL, CAQ, CAS, CAU, CHO, CUN, GUV, HUI, LAG, MET, QUI, RIS, SAN, TOL, VAC

Vítolo & Pearson 2003, Ramírez-Mora 2008, Arenas-Clavijo 2018

Tetracha (Tetracha) spixii (Brullé, 1837)

CHO, MET

Fernández et al 1993, Vítolo & Pearson 2003

Tetracha (Tetracha) sommeri (Chaudoir, 1850)

No data

Chaudoir 1850

Oxycheilini Chaudoir, 1860

Cheiloxya Guérin-Méneville, 1855

Cheiloxya binotata (Laporte, 1833)

No data

Fernandez et al 1993, Vítolo & Pearson 2003

Oxycheila Dejean, 1825

Oxycheila aquatica Guérin-Méneville, 1843*

CUN, SAN, VAC

Wiesner 1999

Oxycheila binotata Gray, 1832

No data

Wiesner 1999

Oxycheila brzoskai Wiesner, 1999*

ANT, NAR, VAC

Cassola & Pearson 2001, Vítolo & Pearson 2003, Ramírez-Mora 2008

Oxycheila chestertonii Bates, 1872

ANT, CUN, MET, TOL, VAC

Wiesner 1999, Vítolo & Pearson 2003, Ramírez-Mora 2008

Oxycheila femoralis Laporte, 1833

CUN, TOL

Vítolo & Pearson 2003

Oxycheila gracillima Bates, 1872

AMA

Vítolo & Pearson 2003

Oxycheila haenschi Horn, 1900

AMA

Vítolo & Pearson 2003

Oxycheila howdeni Brouerius van Nidek, 1980*

ANT, BOL, CAU, VAC

Wiesner 1999, Vítolo & Pearson 2003, Arenas-Clavijo 2018

Oxycheila pearsoni Wiesner, 1999*

ANT, CAU

Wiesner 1999, Vítolo & Pearson 2003

Oxycheila polita Bates, 1872

No data

Wiesner 1999, Vítolo & Pearson 2003

Oxycheila pseudoaquatica Wiesner, 1999*

VAC

Wiesner 1999, Vítolo & Pearson 2003

Oxycheila pseudostrandi Wiesner, 1999*

CAU, NAR

Vítolo & Pearson 2003

Oxycheila tristis (Fabricius, 1775)

No data

Wiesner 1999

Pseudoxycheila Guérin-Méneville, 1839

Pseudoxycheila atahualpa Cassola, 1997

BOY, PUT, SAN

Cassola 1997

Pseudoxycheila bipustulata (Latreille, 1811)*

ANT, BOY, CAL, CAU, CES, CHO, COR, CUN, HUI, MAG, MET, NAR, NSA, PUT, QUI, RIS, SAN, SUC, TOL, VAC

Vítolo & Pearson 2003, Ramírez-Mora 2008, Arenas-Clavijo 2018

Pseudoxycheila caribe Cassola, 1997

NSA

Cassola 1997

Pseudoxycheila ceratoma Chaudoir, 1865*

No data

Vítolo & Pearson 2003

Pseudoxycheila chaudoiri Dokhtouroff, 1882*

BOY, CAL, CAU, MET, QUI, RIS, VAC

Cassola 1997, Vítolo & Pearson 2003

Pseudoxycheila columbiana Cassola, 1997*

BOY, CAU, CUN, MAG, MET, SAN, TOL, VAC

Cassola 1997, Vítolo & Pearson 2003

Pseudoxycheila confusa Cassola, 1997

ANT, BOY, CAU, CES, CAL, CAS, CHO, CAQ, CUN, HUI, MET, RIS, SAN, TOL, VAC

Cassola 1997, Vítolo & Pearson 2003

Pseudoxycheila lateguttata Chaudoir, 1844

ANT, BOY, CAU, HUI

Cassola 1997, Vítolo & Pearson 2003

Pseudoxycheila macrocephala Cassola, 1997*

ANT, CAL, PUT

Cassola 1997, Vítolo & Pearson 2003

Pseudoxycheila nitidicollis Cassola, 1997

HUI, PUT

Cassola 1997, Vítolo & Pearson 2003

Pseudoxycheila tarsalis Bates, 1869*

No data

Cassola & Pearson 2001, Vítolo & Pearson 2003


1 Universidad del Valle. Cali, Colombia.
2 CNRS – Université Toulouse Jean Jaurès, UMR 5608 TRACES, Toulouse, France.

Recibido: 7 de abril de 2021; Aceptado: 28 de junio de 2021

Abstract

The beetle families Carabidae and Cicindelidae, with about 40 000 species worldwide, play an increasing role in biodiversity conservation and ecological studies in Colombia, which makes a faunistic update all the more necessary. We present and analyze a checklist of the species so far described or registered from Colombia until 2020, based on published studies, and their distribution data at the department level. Carabidae are represented by 625 species and Cicindelidae by 100. Magdalena, Cundinamarca and Valle del Cauca are the departments with the highest record numbers of Carabidae, while Cicindelidae are most frequently cited from Valle del Cauca, Antioquia and Meta. The greater sampling effort in these regions is likely due to the accessibility of their natural areas from the main towns. The geographical distribution of Cicindelidae is better documented, with only 17 % of the species without mention of specific localities within the country, against 40 % in Carabidae. Hyper-diverse regions, such as the Chocó and the Amazon, are underrepresented. The number of species currently recorded is therefore estimated to be much lower than true diversity for both families.

Key words:

Biodiversity, Faunistics, Ground beetles, Species list, Tiger beetles..

Resumen

Las familias Carabidae y Cicindelidae, con cerca de 40 000 especies a nivel mundial, tienen un papel creciente en estudios de biodiversidad y ecología en Colombia, lo que hace necesaria una puesta al día de los conocimientos sobre su diversidad. Presentamos y analizamos la lista de las especies descritas/registradas en Colombia hasta 2020, con base en estudios publicados, y sus datos de distribución a escala de departamento. Los Carabidae están representados por 625 especies y los Cicindelidae por 100. Magdalena, Cundinamarca y Valle del Cauca presentan los mayores números de registros de Carabidae, mientras que para Cicindelidae son Valle del Cauca, Antioquia y Meta. Probablemente, el mayor esfuerzo de muestreo en estas regiones se debe a la accesibilidad de sus áreas naturales desde las principales ciudades. Los Cicindelidae se benefician de más registros de localidad, con solo 17 % de las especies sin mención de localidad específica en el territorio nacional, contra el 40 % en Carabidae. Regiones hiperdiversas, como el Chocó y la Amazonía, están subrepresentadas. Por consiguiente, se estima que el número de especies actualmente citadas es muy inferior a la diversidad real de las dos familias.

Palabras clave:

Biodiversidad, Escarabajos del suelo, Escarabajos tigre, Faunística, Lista de especies..

Introduction

Geadephaga, the group of terrestrial Adephaga formed by Carabidae (ground beetles), Cicindelidae (tiger beetles) and Trachypachidae, with about 40 000 described species worldwide, represents nearly 10 % of the species so far described in the order Coleoptera (Bouchard et al., 2017; Lorenz, 2017). Within this monophyletic group (López-López & Vogler, 2017), the position of tiger beetles is still under debate, whether as Cicindelidae at family rank (López-López & Vogler, 2017; Duran & Gough, 2020) or as Cicindelinae within Carabidae (Gough et al., 2019; Li et al., 2020). In this study, we provisionally placed tiger beetles at family rank without prejudice to future advances in genomic studies, because in most studies they have been treated separately from ground beetles. Trachypachidae, on their part, are not represented in the Neotropics.

Carabidae and Cicindelidae are present in almost every possible ecosystem worldwide (Lövei & Sunderland, 1996), with a great diversity of life history traits, and frequently used as bioindicators in ecological studies (Rainio & Niemelä, 2003; Pearce & Venier, 2006) or as control agents against agricultural pests, due to their predatory habits (Kromp, 1999; de Heij & Willenborg, 2020). Therefore, their knowledge can be crucial in studies on sustainable agriculture, or on assessment of vulnerable natural areas.

Information on Geadephaga of Colombia has been synthetized in two studies more than fifteen years ago: one by Vítolo (2004) on Cicindelidae, and another by Martínez (2005) on Carabidae. Vítolo (2004) offers data on morphology, distribution in Colombia, identification keys, and a summary of the diversity of tiger beetles in the country. Martínez (2005) provides identification keys with full habitus illustrations for all the genera present in Colombia. As the main objective of the latter study was to allow identification at the genus level, the information on the distribution of taxa was also limited to genera. Moreover, the list of species in Martínez (2005) needs revision in three aspects: some species cited from Colombia in the scientific literature were not included, the presence in Colombia of other species is stated without references, and a few unnamed morphospecies are listed, which hinders a correct evaluation of the total number of species cited from Colombia. As a complement to these fundamental works, Moret (2003) published an identification key to the Carabidae of the Andean paramo which includes southern Colombia, but it is also limited to genera and does not provide any distributional information.

In Colombia, the uncertainty about the identity of many species (Linnaean shortfall) and their spatial distribution (Wallacean shortfall) are the greatest obstacles to develop robust ecological studies (Hortal et al., 2015). In addition, poor taxonomic and faunistic knowledge limits the potential assessment of the ecosystem services that these beetles could provide. Parataxonomy (i.e. the assignation of individuals to morphospecies based on their external appearance, without considering neither taxonomic literature nor the specialists within the group), as an alternative way to overcome the taxonomic impediment in ecological studies, appears to be an unsatisfactory solution, since it tends to overestimate the number of species and does not guarantee reproducibility (Krell, 2004).

The knowledge of Colombian Geadephaga has increased in recent years, due to a growing number of taxonomic (e.g. Arenas-Clavijo, 2017; Forero et al., 2019; Moret, 2019; Sarmiento-Roa et al., 2020) and ecological studies (e.g. Arenas & Armbrecht, 2019; García-Suabita et al., 2019) based on this group during the last decade. An update of the current taxonomic and faunistic knowledge was therefore necessary, as a starting point for future systematic revisions of the tribes or genera which might deserve special attention from a biogeographical or ecological point of view.

For these reasons, the present study aims to list the Carabidae and Cicindelidae species recorded from Colombia in the literature, up to 2020, thus offering a current state of knowledge of these two families, emphasizing gaps and biases. It also seeks to provide information on areas of potential interest, where it would be convenient to intensify, complete or initiate samplings of these ecologically important beetles.

Material and methods

Bibliographic database

A total of 150 studies published up to 2020, related to ground and tiger beetles of Colombia, was obtained from an exhaustive search that included documents from the 19th century. Much of this literature is available in electronic repositories (e.g. Biodiversity Heritage Library, Gallica, Persée), and a smaller portion was gathered by direct request to libraries or authors. The reviewed publications cover the following topics: (1) descriptions of new species based on material from Colombia or, in the mid-19th century studies, from “Nueva Granada” or “Nouvelle Grenade”; (2) new Colombian records of species already described from other countries; (3) lists of species of a genus or of a supra-generic taxon in systematic revisions; and (4) ecological studies or biodiversity inventories. Regarding the last category, doubtful attributions marked as “cf.” or “aff.”, as well as morphospecies designated by a number, were not included. Based on this inventory, the references of all the species listed by Martínez (2005) were verified (Appendix 1), and a new checklist was produced.

Construction of the checklist

Once the references were compiled, a list was constructed in which species are sorted by genus. Infraspecific taxa were excluded from the list. Generic and subgeneric names were updated in accordance with Lorenz (2017) or based on the last available systematic revisions. In the case of synonyms or debated generic attribution, we followed as a general rule the taxonomic decision of the most recent revision, the reference of which is given in the bibliographic section of the list (Appendix 2, last column). Locality information is limited to the “Departamento” (department or province), and only published localities were taken into account.

Data analysis

The checklist was used as a database to build graphs and maps to better understand the current state of knowledge of the group in Colombia. These graphs are based on the description year or on the year of the first record for each species, on the number of species per genus, and on the number of species per department.

Results

Carabidae

Based on published data, the family Carabidae is currently represented in Colombia by 625 species -close to 1.7 % of the world total-, arranged in 10 subfamilies, 32 tribes and 125 genera (Appendix 2). Of the recorded species, 330 (53 %) have not been reported from any other country, so that could be considered Colombian endemics, at least until they do not get recorded from any surrounding country. Thirteen genera account for 50 % of the species, the most speciose genus being DyscolusDejean, 1831 (Harpalinae, Platynini), which contains 14 % of the total (85 species) (Figure 1). Forty-seven genera (38 %) are represented by a single species in Colombia (Table 1), five of which are monospecific, with records of their unique species in at least another country: Stenocheila (Harpalinae, Lachnophorini); Askalaphium (Harpalinae, Ctenodactylini); Enceladus (Siagoninae, Siagonini); Homalomorpha (Harpalinae, Cratocerini) and Trichognatha (Harpalinae, Galeritini) (Martínez 2003, 2005; Martínez & Ball, 2003; Lorenz, 2017). Three genera are only known from Colombia: Callidadelpha (Harpalinae, Lebiini), Cryptomma (Scaritinae, Clivinini) (without specific locality recorded) and Columbitrechus (the latter, most likely a synonym of Paratrechus). Finally, two introduced species have been registered: Laemostenus complanatus, from northern Africa and/or western Europe (Martínez, 2005), and Mochtherus tetraspilotus, from southeastern Asia (Torres-Domínguez et al., 2020).

Number and proportion of species by genus of ground beetles recorded from Colombia

Figure 1: Number and proportion of species by genus of ground beetles recorded from Colombia

Table 1: Structure of the subfamilies and tribes of Carabidae Latreille, 1802 in Colombia. In parentheses: number of genera with only one species recorded in the country.

Regarding species geographic distribution, 254 species (~41 %) are known from the country as a whole without more precise localities, from which 143 have not been cited from any other country; 371 species (~59 %) have at least one specific locality record. 309 species are known from a single department (Figure 4), and 163 of these are exclusive to Colombia. The departments with the highest number of recorded species are: Magdalena (79), Cundinamarca (75) and Valle del Cauca (43), while Guaviare, San Andrés y Providencia and Sucre have no records for the family (Appendix 1, Figures 2 and 3).

Number of ground beetle species per Colombian departments.

Figure 2: Number of ground beetle species per Colombian departments.

Number of ground beetle species per Colombian department, based on data published from 1831 to 2020.

Figure 3: Number of ground beetle species per Colombian department, based on data published from 1831 to 2020.

Number and proportion of species by genus of tiger beetle recorded from Colombia.

Figure 4: Number and proportion of species by genus of tiger beetle recorded from Colombia.

The species with the widest distribution in Colombia are Laemostenus (Laemostenus) complanatus (Harpalinae, Sphodrini) and Pelmatellus variipes (Harpalinae, Harpalini), each one with locality data in 11 departments (Camero, 2003; Martínez & Ball, 2003), but most of the species with the widest distribution belong to the tribe Platynini. However, in some cases, systematic revisions could reveal the existence of several species with more limited distributions under the currently accepted name.

Cicindelidae

The family Cicindelidae is currently represented in Colombia by 100 species distributed in three tribes and 21 genera of the subfamily Cicindelinae (Appendix 3). This figure represents 3.3 % of the world total of tiger beetle species, a percentage twice as high as in Carabidae. Of the species registered in the Colombian territory, 16 do not have records in any other country, most of them probably endemic according to the available data. The most diverse genus is Odontocheila, with 16 species, while 81 % of the remaining species is contained in seven different genera (Figure 4).

Eight tiger beetle genera are represented by a single species in Colombia (Table 2), but none has a distribution limited to the country. Callidema boussingaulti (Cicindelini) has a restricted distribution in mountain environments, since it is known only from the Andes of Colombia, Peru and Ecuador (Cassola & Pearson, 2001). Other genera such as Cheiloxya (Cicindelini), Cenothyla (Cicindelini) and Ronhuberia (Cicindelini) are distributed in northern South America (Cassola & Pearson, 2001; Moravec, 2020).

Table 2: Structure of the subfamilies and tribes of Cicindelidae Latreille, 1802 in Colombia. In parentheses: number of genera with only one species recorded in the country.

Regarding the distribution of Cicindelidae in Colombia, 17 species (17 %) do not have any precise locality records, three of which appear to be endemic to the country: Odontocheila simulator, although the holotype and only known specimen of this dubious taxon is probably an artefact (Moravec, 2018); Pseudoxycheila ceratoma; and Pseudoxycheila tarsalis (Cicindelini). 21 species are known from only one department (Figure 5), and of these, four are not recorded from other countries: Odontocheila hamulipenis and Oxycheila pseudoaquatica (Cicindelini) from Valle del Cauca; Oxygonia kippenhani from Boyacá; and Ctenostoma (Procephalus) maculosum (Ctenostomatini) from Cundinamarca (Appendix 3).

Distribution of tiger beetle species in Colombia, per departments.

Figure 5: Distribution of tiger beetle species in Colombia, per departments.

The departments with the highest number of tiger beetle species records are Valle del Cauca (36), Antioquia (27) and Meta (27), whereas San Andrés, Providencia and Arauca do not have records (Appendix 3 and Figure 6). Vaupés department, with only one record (Odontocheila trilbyana), is located in the Amazonia, a region where many tiger beetle species have already been reported in neighboring countries, which highlights the low level of sampling of this ecosystem in Colombia.

Number of tiger beetle species per Colombian department, based on data published from 1842 to 2020.

Figure 6: Number of tiger beetle species per Colombian department, based on data published from 1842 to 2020.

The species with the widest distribution in Colombia are Pseudoxycheila bipustulata, with records in 20 departments, and Tetracha (Tetracha) sobrina in 19 (Appendix 3). Regarding the genus PseudoxycheilaVítolo (2004) expressed doubts about the status of some species proposed by Cassola (1997), as species differentiation is especially difficult in this Andean genus, and several of the new species described by Cassola appear to fall within the morphological variation range of P. bipustulata. In this case, as in many others, a molecular approach would be necessary to solve the issues left by conventional morphology-based taxonomy.

Discussion

The current knowledge of the families Carabidae and Cicindelidae in Colombia is the result of a two centuries-long history (Figure 7).Regarding Carabidae, taxonomic descriptions based on material from Colombia began as early as 1825,but they reached their greatest development between the second third and the end of the 19th century, a period in which 70 % of the carabid fauna known from the country had already been described, mainly thanks to the contributions of Louis Reiche (52 species described- between 1842 and 1843), Maximilien de Chaudoir (131 species described between 1848 and 1880) and Jules Putzeys (89 species described between 1846 and 1878). In this period, most descriptions were very brief, not illustrated, with limited distribution data or without any, and they did not fit the current standards of insect taxonomy. Furthermore, very few have been subject to taxonomic revisions in recent times, which makes their identification difficult, if not impossible without examining type specimens.

Cumulative number of ground beetle species described (in blue) and recorded from Colombia (in orange), in five-years increments, up to 2020. Species described from Colombia but subsequently synonymized are not included.

Figure 7: Cumulative number of ground beetle species described (in blue) and recorded from Colombia (in orange), in five-years increments, up to 2020. Species described from Colombia but subsequently synonymized are not included.

The genera in which this situation is especially detrimental are Dyscolus, Notiobia, Lebia and Agra,among others. From the beginning of the twentieth century, the rate of description of new species has been very slow, with a slight rebound from 1980. The new records from Colombia (i.e. for species whose description was based on specimens from other countries) have followed a much slower pace, with a gradual increase from the mid-20th century, when authors such as Stefano Straneo (records from Colombia from 1951 to 1991), Joaquim Mateu (1961-1998), George E. Ball (1978-2013), Terry L. Erwin (1970-2016), Danny Shpeley (1978-2013) , among others, contributed to the knowledge of the fauna of Colombia.

The investigations on Cicindelidae followed a different path (Figure 8). The pace of descriptions was globally slow, with two acceleration points: a weak one during the second third of the 19th century, with contributions by several authors who published isolated species descriptions, and another very strong in the last decade of the twentieth century, based on more comprehensive works, especially revisions of genera at a continent scale, such as those by Fabio Cassola (1997), Roger Naviaux (1998), Jürgen Wiesner (1992), 1999). Thanks to these taxonomic revisions and to several local, national or continental checklists (Cassola & Pearson, 2001; Fernández et al., 1993; Moravec 2018, 2020; Vítolo & Pearson, 2003; Wiesner, 2020), Colombian records of species described from other countries increased dramatically since 1990, exceeding the number of new descriptions. In this regard, tiger beetle knowledge has progressed much faster in recent decades than that of ground beetles. This greater sampling and publication effort may also explain why the Colombian records amount to 3.3 % of the world total of tiger beetle species, a percentage twice as high as in Carabidae.

Cumulative number of tiger beetle species described from Colombia (in blue) and recorded from Colombia (in orange), in five-year increments, up to 2020. Species described from Colombia but subsequently synonymized are not included.

Figure 8: Cumulative number of tiger beetle species described from Colombia (in blue) and recorded from Colombia (in orange), in five-year increments, up to 2020. Species described from Colombia but subsequently synonymized are not included.

The geographical distribution of the locality records of Carabidae (Figure 3) is largely due to accessibility factors. In most cases, naturalists of the 19th century and the first half of the 20th century were constrained by the reduced transportation network of that time and collected along the same routes around the main cities. Natural areas near main roads and navigable rivers were the most surveyed, which creates an over-sampling bias and makes it difficult to assess the true diversity of each region, in line with the results of a study performed in a neighboring country (Donoso et al., 2009). Another kind of bias derives from the activity of a particular researcher in a limited area. For example, most of the species reported from the Magdalena department correspond to species of the genus Blennidus, described by Stefano Straneo from specimens collected by Philip J. Darlington in the Sierra Nevada de Santa Marta in 1928 and 1929.Conversely, ground beetle diversity is clearly underestimated in less accessible hyper-diverse regions such as the Chocó ecoregion, the Amazon foothills (Caquetá and Putumayo departments) and the Amazon rainforest itself (Guainía, Guaviare and Vaupés departments). Although true diversity cannot be precisely assessed based on available data, it is expected that these regions have a more diverse carabid fauna than what is currently known.

The distribution of tiger beetle records throughout the Colombian territory (Figure 6) is more balanced than that of ground beetles, possibly due to the interest the group has provoked among professional and amateur entomologists over the last decades.

When comparing the number of Geadephaga species recorded so far from Colombia (725) with that of other countries, it appears clearly that there is still a huge work ahead before approaching a complete knowledge of their diversity in this country.

Our results in Colombia are comparable to those obtained in Peru, where 690 species are currently known (Erwin et al., 2015, leaving aside unnamed morphospecies only designated by numbers) in a territory of a size similar to that of Colombia. In Brazil, a territory eight times larger, 1506 species have been reported, that is, only twice as many (Roig Juñent & Domínguez, 2001).

The level of knowledge is higher in Ecuador, with 763 species (Moret & Salazar, unpublished data) in a territory five times smaller and in ecosystems shared with southern Colombia: Chocó ecoregion, Andean montane forest, paramo, interandean dry shrublands or woodlands, Amazonian lowlands. Outside the Neotropics, to mention just one example, 693 species have been reported in the state of Texas in the United States of America (Bousquet, 2012), a territory twice as small.

The magnitude of the work to be done is obvious when noting that the late Terry L. Erwin collected more than 600 species of Carabidae (most of which remain undescribed) in the Pakitza reserve of Peruvian Amazonia, in a space of only 40 km2 (Erwin, 1991), that is, a number close to the total of the described species registered for the whole of Peru. In Colombia, the number of recorded species does not exceed 42 in any of the six departments (Nariño, Putumayo, Caquetá, Cauca, Huila, Meta) which contain environments similar to that of Pakitza, i.e. lower montane forest at an elevation of about 650 m in the Amazonian foothills of the Andes.

Conclusion and perspectives

The results of this study suggest that the deficient taxonomic and chorological knowledge of the families Carabidae and Cicindelidae in Colombia will be an obstacle to developing well supported ecological studies of this group, as long as species distributions are not accurately known. Publication of distributional information based on reliable identifications, as well as taxonomic revisions of the genera offering the highest value as bioindicators or pest control, are therefore urgent priorities.

Another challenge faced by the study of Geadephaga in Colombia is the possibility of reaching the specific level in identifications, an issue that can be of great importance in ecological studies. The identification keys currently available for Colombia (Moret, 2003; Martínez, 2005; Vítolo, 2004) are limited to the genus level. Species-level keys exist for a number of neotropical genera (e.g. Arndt, 1998; Ball & Shpeley, 2009; Boyd & Erwin, 2016), but they include species not found in Colombia and are therefore difficult to use by non-taxonomic biologists. Developing keys for all genera of ground beetles and tiger beetles recorded in Colombia is currently an unachievable goal, but it would be desirable to focus efforts on a small number of genera including a sufficient number of described species and of interest as bioindicators.

Finally, in the light of current knowledge and the available techniques, two paths are needed to improve future studies of ground beetles in Colombia: (1) compare specimens deposited in Colombian collections with types kept in European and North American museums, to generate valid vouchers for local taxonomists, and (2) retrieve molecular data (e.g. COI-based DNA barcodes) from these local vouchers, to facilitate future research.

Acknowledgments

We warmly thank Jiri Moravec for providing recent literature on Odontocheilina (Cicindelidae), Petr Bulirsch for useful comments on the systematics of Scaritinae (Carabidae), and Fernanda Salazar for her help in the construction of the database and information on the Ecuadorian carabid fauna. We especially thank Dione Seriperri, Museu de Zoologia, Universidade de São Paulo, for her help in finding publications by Hans Reichardt. AAC’s doctoral studies were partly funded by the “Fondo nacional de financiamiento para la ciencia, la tecnología y la innovación, Francisco José de Caldas”, contract number 491-2020 in program 1106-852-70306 “Relaciones multiescalares de la diversidad en gradientes altitudinales del bosque tropical”, project 70899 “Diversidad de artrópodos en gradientes altitudinales: una aproximación integrativa morfológica y molecular”. Finally, but not last, we thank the comments of two anonymous reviewers, which helped to improve the manuscript.

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Appendix 1. Bibliographic references reviewed to generate the species list of Geadephaga present in Colombia.

Arenas, A., Armbrecht, I. & Chacón, P. (2013). Carábidos y hormigas del suelo en dos áreas cultivadas con maracuyá amarillo (Passiflora edulis) en el Valle del Cauca, Colombia. Acta Biológica Colombiana, 18(3), 439-448.

Arenas-Clavijo, A. & Armbrecht, I. (2019). Soil ants (Hymenoptera: Formicidae) and ground beetles (Coleoptera: Carabidae) in a coffee agroforestry landscape during a severe-drought period. Agroforestry Systems, 93, 1781-1792

Arenas-Clavijo, A., & Chacón de Ulloa, P. (2016). Escarabajos terrestres (Coleoptera: Carabidae) de fragmentos de bosque seco en el valle geográfico del río Cauca, Colombia. Boletín del Museo de Entomología de la Universidad del Valle, 16(2), 18-25.

Arenas-Clavijo, A. & González, R. Carabidae (Coleoptera) del Parque Nacional Natural Gorgona, Cauca-Colombia: un informe preliminar. Boletín del Museo de Entomología de la Universidad del Valle, 18(2), 13-21.

Arenas-Clavijo, A. & Posso-Gómez, C. E. (2017). Carábidos (Coleoptera: Carabidae) del Museo de Entomología de la Universidad del Valle (Cali, Colombia). Biota Colombiana , 18(2), 267-273.

Arenas-Clavijo, A. (2017). Primer registro de Notiobia (Notiobia) umbrifera Bates y redescubrimiento de Notiobia (Anisotarsus) praeclara Putzeys (Coleoptera: Carabidae) en Colombia. Boletín Científico del Centro de Museos. Museo de Historia Natural, 21(1), 226-233.

Arenas-Clavijo, A. (2018). Escarabajos tigre (Coleoptera: Cicindelidae) del Museo de Entomología de la Universidad del Valle, Colombia. Boletín del Museo de Entomología de la Universidad del Valle, 18(1), 32-45.

Arndt, E. (1998). The species of Notiobia Perty (Coleoptera: Carabidae: Harpalini) from Brazil. Acta Amazonica, 28(3), 285-299.

Ball, G. E. & Maddison, D. R. (1987). Classification and evolutionary aspects of the species of the New World genus Amblygnathus Dejean, with description of Platymetopsis, new genus, and notes about selected species of Selenophorus Dejean (Coleoptera: Carabidae: Harpalini). Transactions of the American Entomological Society, 113(3), 189-307.

Ball, G. E. & Shpeley, D. (1992). Appendix - Geographical distribution and evolution of the Selenophori (Harpalini) and Apenes LeConte (Lebiini) in the Antilles (Coleoptera: Carabidae). In Noonan, G. R., Ball, G. E. & Stork, N. E. (Eds. ). The Biogeography of Ground Beetles of Mountains and Islands. Pp: 94-121. Newcastle: Intercept.

Ball, G. E. & Shpeley, D. (2002). The neotropical subgenera and species of the pantropical genus Anaulacus MacLeay (sensu novo) (Coleoptera: Carabidae: Masoreini): a taxonomic revision, with notes about way of life, evolution, and geographical history. Transactions of the American Entomological Society, 128, 265-343.

Ball, G. E. & Shpeley, D. (2005). Taxonomic review of the Tribe Melaenini (Coleoptera: Carabidae), with observations on morphological, ecological and chorological evolution. Zootaxa, 1099, 1-120.

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Vítolo, A. (2004). Guía para la identificación de los escarabajos tigre (Coleoptera: Cicindelidae) de Colombia. Instituto de Investigación de Recursos Biológicos Alexander von Humboldt. 198 pp.

Whitehead, D. R. (1972). Classification, phylogeny, and zoogeography of Schizogenius Putzeys (Coleoptera: Carabidae: Scaritini). Quaestiones Entomologicae, 8, 131-348.

Wiesner, J. (1992). Checklist of the Tiger Beetles of the world Verlag Erna Bauer Keltern, 364pp.

Wiesner, J. (1999). The tiger beetle genus Oxycheila (Insecta: Coleoptera: Cicindelidae) 50th contribution towards the knowledge of Cicindelidae. Schwanfelder Coleopterologische Mitteilungen; 3, 1-81.

Will, K. W. (2002). Revision of the new world abariform genera Neotalus n. gen. and Abaris Dejean (Coleoptera: Carabidae: Pterostichini (Auctorum). Annals of the Carnegie Museum of Natural History, 71, 143-213.

Will, K. W. (2005). The Neotropical genera Oxycrepis Reiche and Stolonis Motschulsky: a taxonomic review, key to the described species and description of new Stolonis species from Ecuador (Coleoptera: Carabidae: Loxandrini). Zootaxa, 1049, 1-17.

Zamorano, L. S., Erwin, T. L. & Kavanaugh, D. H. (2019). Nomenclatural changes in the Lachnophorini (Coleoptera: Carabidae) of the Western Hemisphere. The Coleopterists Bulletin, 73(1), 121-126.

Appendix 2

Appendix 2: List of species of Carabidae Latreille, 1802 recorded from Colombia until 2020, with their respective distribution within the country. Species marked with asterisk (*) have been cited only from Colombia. Departments are codified according to ISO rule 3166-2. References are listed in appendix 1.

Appendix 3

Appendix 3: List of species of Cicindelidae Latreille, 1802 from Colombia until 2020, with their respective distribution within the country, species marked with asterisk (*) have been cited only from Colombia. Departments are codified according to ISO rule 3166-2. References are listed in appendix 1.

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Cómo citar

Arenas, A., Montoya-Lerma, J. ., & Moret, P. . (2022). Diversidad de Geadephaga (Coleoptera: Carabidae y Cicindelidae) en Colombia: una aproximación desde la literatura existente. Biota Colombiana, 23(1), e962. https://doi.org/10.21068/2539200X.962
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