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Article

A New Peyritschiella Species (Laboulbeniales, Ascomycota) on Staphylinidae (Coleoptera, Insecta) from the Tropical Montane Cloud Forest of Mexico †

by
Ericka Lorena Ortiz-Pacheco
1,
Tania Raymundo
1,
Silvia Bautista-Hernández
1,*,
Juan Márquez
2 and
Julieta Asiain
2
1
Laboratorio de Micología, Departamento de Botánica, Escuela Nacional de Ciencias Biológicas, Instituto Politécnico Nacional, Prolongación de Carpio y Plan de Ayala s/n, Col. Santo Tomás, Miguel Hidalgo, Ciudad de México 11340, Mexico
2
Laboratorio de Sistemática Animal, Centro de Investigaciones Biológicas, ICBI, Universidad Autónoma del Estado de Hidalgo, Mineral de la Reforma, Hidalgo 42184, Mexico
*
Author to whom correspondence should be addressed.
Taxonomy 2025, 5(4), 53; https://doi.org/10.3390/taxonomy5040053
Submission received: 26 July 2025 / Revised: 19 September 2025 / Accepted: 29 September 2025 / Published: 4 October 2025

Abstract

One new species of Laboulbeniaceae, Peyritschiella styngeti, is described and illustrated. It is characterized by appendages with a black constriction at the base, perithecia with four papillae on the apical zone, cruciform bilateral symmetry, and an extremely melanized receptacle. This species was observed on the stylus of the staphylinid Styngetus deyrollei, which is distributed in tropical montane cloud forests in Mexico. Currently, the Laboulbeniales mycobiota in Mexico comprises 82 species, with 11 described growing on species of the Staphylinidae family. Additionally, a compilation of the Laboulbeniales species reported for Mexico and for Staphylinidae species is presented.

1. Introduction

Peyritschiella Thaxt. 1890 [1] is a genus taxonomically located in the Laboulbeniaceae family. Some of its diagnostic characteristics include that it presents a receptacle conformed by the following four overlapped areas: a basal area, a sub-basal area, a subterminal area, and a terminal area where the perithecia develop, which are symmetric and possess papillae on the apical zone. The antheridia are conical-shaped, continuous, and divided from the receptacle by a constricted dark-colored basal zone, and the ascospores are septate [2]. Thaxter [3,4] states that it is a very particular group because there is no other that possesses a compound antheridium and the receptacle’s bilateralism, as these characteristics are only shared with Dimorphomyces Thaxt. 1890 [1]. Haelewaters et al. [4] mention that the order to which Peyritschiella is part of, Laboulbeniales, has representative hosts from the Insecta class, subphyla Myriapoda and Chelicerata.
Laboulbeniales are considered obligate ectoparasites that rely on their hosts and exhibit a high degree of specificity. As stated by Van der Linde and Rhong [5], their distribution corresponds to that of their hosts, and they depend on these hosts to acquire the necessary resources for their life cycle, sustenance, and survival within insect populations. Their transmission method has been observed to be highly effective, involving direct contact between insects, including sexual reproduction and chance encounters among organisms in large groups displaying social behaviors. This facilitates the spores’ contact with non-infected organisms, allowing them to penetrate the cuticle and successfully develop their thallus. The environment may also serve as a secondary intermediary, albeit with a lower success rate, maintaining spore viability through soil humidity [6,7]. All these factors contribute to the specificity of Laboulbeniales, which grow only in certain regions of their hosts, resulting in a wide range of morphologies based on the area of infection they develop [8], making them, by estimation, the most diverse group of fungi [6], adding to the group’s peculiarities, such as the proliferation of the thalli by the division of the ascospore cells instead of developing a mycelium; the apparent lack of an asexual reproductive stage; and the impossibility of growing them ex situ [6].
In Mexico, studies of Laboulbeniomycetes have been almost nonexistent. The first study on this group [9] was conducted on the genus Rickia Cavara 1899 [10], which grows on passalid beetles (Coleoptera: Passalidae). However, Mexican records have been mentioned in studies worldwide [2,11,12,13,14,15,16,17,18,19,20,21,22], which are summarized in (Appendix A, Table A1), in which only ten species parasitizing rove beetles have been reported (Appendix B, Table A2). The records state 81 species of Laboulbeniomycetes in the country, of which 78 are located in the Laboulbeniales order and 3 are part of the Herpomycetales order. Until now, there have been no specific studies whatsoever about Laboulbeniales found parasitizing Staphylinidae in Mexico; hence, the objective of the present study is to describe a new species of Peyritschiella for the world’s mycobiota.

2. Materials and Methods

  • Host examination and Thalli removal
The specimens were obtained from Staphylinidae (rove beetles) organisms that were part of the entomological collection integrated into the CC-UAEH (Coleoptera Collection of the Universidad Autónoma del Estado de Hidalgo), which were revised on the head, thorax, and abdomen. There was greater focus on the host’s stylus located in the abdomen’s basal area under the stereoscopic microscope; for this revision, the insects were placed on a Petri dish, with the help of a few drops of 70% alcohol. The thalli were extracted using a periodontal probe by performing light sweeps over the host’s stylus.
  • Morphological characterization
The samples were set as fixed specimens using Hoyer’s reactive, and subsequently sealed with two coats of translucent nail polish. The thallus was characterized, measured with an ocular micrometer, and described in form, color, and number of perithecia, antheridia, and appendages, as well as the foot and visible cells of the receptacle. The taxonomic identification was followed up to the genus using Thaxter’s taxonomic key and descriptions. The fixed specimen preparations of Laboulbeniales are deposited in the ENCB fungi collection located in the Instituto Politécnico Nacional under the following code numbers: ENCB-L01 ELOP01 To ENCB-L104 ELOP106.

3. Results

Ascomycota
Pezizomycotina
Laboulbeniomycetes
Laboulbeniomycetidae
Laboulbeniales
Laboulbeniaceae
Peyritschiella styngeti E.L. Ortiz-Pacheco, Raymundo & Baut.-Hern. sp. nov.
MycoBank No. 857590
  • Diagnosis. Three-leveled receptacle, subtriangular and flattened; hyaline appendages; constricted at the base with an evident dark-brown coloration; symmetrical or almost symmetrical perithecia, presence of papillae on the apical area of the perithecia; hyaline, bicellular ascospores (Figure 1).
  • Etymology. The term styngeti corresponds to the genus in which the host is taxonomically located (Styngetus).
  • Holotype. Mexico • Hidalgo, Molango, Acautitlán; tropical montane cloud forest; 1715 m.a.s.l.; N 20° 45′38.4″, W 88°42′50.7″; squid-baited pitfall trap; 15 to 24 May 2011; J. Márquez, ENCB-L16 ELOP02 (Figure 1J).
  • Description. Thallus 69–280 × 20–64 µm (Figure 1J). Receptacle 50–100 × 20–64 µm, subtriangular and flattened, narrow at the base, wider under the perithecia, of superficial insertion. Receptacle cells are covered by a dark brown color, the last row of a cell arranged in transversal form and curved inwards, building a margin that longitudinally covers the basal area of the perithecia (Figure 1J(b)). Foot cell 4–20 × 9–16 µm, dark colored (Figure 1J(a)). Hyaline appendages, constricted at the base with an evident dark-brown coloration, arranged to the external sides of the perithecia over the longitudinal margin of the receptacle, 10–80 × 2–5 µm (Figure 1J(c)); compound antheridia, arranged laterally over the appendages, only observed in one 15–20 × 6–9 µm thallus (Figure 1E). Perithecia 15–150 × 5–37 µm, located apically (Figure 2 and Figure 3A,B), symmetrical or almost symmetrical, arranged one beside the other, presence of four papillae, cruciform, on the apical area of the perithecia (Figure 1D and Figure 4B); hyaline, bicellular ascospores 40–56 × 4–5 µm, fusiform, septate and covered with a mucilage which helps adhesion to the host (Figure 1I and Figure 3C,D).
  • Other Specimens examined of Styngetus deyrollei. Hidalgo, Tlanchinol, camino a Apantazol, El Pozo; tropical montane cloud forest, 1391 m.a.s.l.; squid-baited pitfall trap No. 2; 1 to 22 October 2011; J. Márquez.; Zacualtipán; squid-baited pitfall trap No. 2; 20 September to 4 October 2011.; Zacualtipán; tropical montane cloud forest; N 20°38′44.5″, W 98° 36′7.2″; squid-baited pitfall trap No. 6; 14 to 28 April 2011; MA.; Zacualtipán, camino a Tizapán; tropical montane cloud forest; N 20°38′44.5″, W 98°36′7.2″; squid-baited pitfall trap; 14 to 28 May 2011; J. Márquez.; Molango, Acuatitlán; tropical montane cloud forest; 1715 m.a.s.l.; N 20°45′38.4″, W 88°42′50.7″; flight interception trap No. 1; 15 to 29 April 2011; J. Márquez.; La Misión, Los Naranjos-Palo Hueco; tropical montane cloud forest; 1715 m.a.s.l.; N 21°08′06″, W 99°05′02″; 10 to 24 March 2011; J. Márquez.; La Misión, Las Pilas; tropical montane cloud forest; flight interception trap; 12 to 19 July 2018; A. Lora and J. Márquez.; Tlanchinol, camino a Apantazol, El Pozo; tropical montane cloud forest; 1391 m.a.s.l.; N 20°59′6.73″, W 98°37′39.86″; flight interception trap No, 1; 16 to 30 April 2011; J. Márquez.; Tlanchinol; tropical montane cloud forest; 1391 m.a.s.l.; N 20°59′6.73″, W 98°37′39.86″;squid-baited pitfall trap No. 2; 16 to 30 April 2011.; Molango, Acuatitlán; tropical montane forest; 1715 m.a.s.l.; N20°45′38.4″, W 88°42′50.7″; squid-baited pitfall trap No. 4; 15 to 29 April 2011; J. Márquez.; Tlanchinol, camino a Apantazol, El Pozo; tropical montane cloud forest; 1391 m.a.s.l.; N 20°59′6.73″, W 98°32′39.86″; squid-baited pitfall trap; 16 to 30 April 2011; J. Márquez.; La Misión, Lagunita de Pilas; tropical montane cloud forest; squid-baited pitfall trap No. 2; 17 February to 17 March 2019; A, Lora.; Zacualtipán, camino a Tizapán; tropical montane cloud forest; 1790 m.a.s.l.; N 20°38′44.5″, W 98°36′7.2″; squid-baited pitfall trap; 14 to 28 April 2011; J. Márquez.; La Misión, Lagunita de Pilas; tropical montane cloud forest; 1770 m.a.s.l.; N 21°7′38″, W 99°6′53″; dung-baited pitfall trap; 11 June to 10 July 2019; J. A. Lora.; Tenango de Doria, La Viejita; tropical montane cloud forest; 1163 m.a.s.l.; N 22°47′58″, W 57°66′07″; squid-baited pitfall trap; 12 August 2010; C. Cornejo.; Tlanchinol, camino a Apantazol, El Pozo; tropical montane cloud forest; 1391 m.a.s.l.; N 20°59′6.732″, W 98°37′39.86″; squid-baited pitfall trap No. 1; 16 to 30 April 2011; J. Márquez. • Puebla, Zacapoaxtla, Apulco, Cascada La Gloria; tropical montane cloud forest; squid-baited pitfall trap; 18 May to 28 May 2021; J. Márquez and J. Asiain. • San Luis Potosí, Las Pozas de James; tropical montane cloud forest; squid-baited pitfall trap; 17 July 2007; J. Asiain, APMP, IAA, MY, J. Márquez. (ENCB).
  • Host. Obligate ectoparasite of Styngetus deyrollei, specifically located on the stylus on both males and females (Figure 1A); host with predaceous habits in the tropical montane cloud forest. Other rove beetles’ specimens were revised (Philonthus, Oligotergus, Platydracus, Chroaptomus), none of them showed infection by this new species.
  • Distribution. Distributed in the states of Hidalgo, Puebla and San Luis Potosí. It is a new species for the worldwide mycobiota.
  • Notes.Peyritschiella styngeti sp. nov. is characterized by the presence of appendages with a dark constriction at the base (Figure 1I), two perithecia with four papillae on the apical area, cruciform aspect (Figure 1D and Figure 4B), bilateral symmetry, and a receptacle conformed by three highly pigmented levels, making it look like it is only one level (Figure 1J). This species is highly specific because it is only found on S. deyrolley’s (Figure 1A) stylus (Figure 1B). The characteristics, as mentioned earlier, differentiate this species from other taxonomically close ones like P. cafiana (Thaxt.) I.I. Tav. 1985 [18], which presents three well-defined leveled receptacle and short appendages. Furthermore, the pigmented area in this same structure is only observed on the foot cell and the adjacent area, and although both species present two lobulated perithecia, the melanization pattern is a very visible characteristic that differentiates it from P. styngeti.
Figure 1. Peyritschiella styngeti, (A) dorsal view of the host Styngetus deyrollei Solsky [23]; (B) stylus of the host which was infected; (C) lateral view of the thallus on a seta from the stylus of the host; (D) apical zone of the perithecia, showing the four papillae, characteristic of the species; (E) antheridia, growing on the apical zone, besides the perithecia, growing apically on the appendages; (F) first stage of the growing thallus, growing on a seta from the stylus of the host, the foot cell has developed and the bottom cell of the ascospore has elongated, the darkened division between booth cells of the ascospore in a dark brown is visible, looking like a small cross, apical cell of the ascospore has not yet grown, the thallus has not developed, and the structures are highly hyaline; (G) thallus developing, foot cell has grown and the receptacle’s cells are developing, apical structures which include perithecia and appendages have not been fully developed; (H) growing thallus, upper level of the receptacle is developing, perithecia growing on the apical are of the receptacle, coloration has darkened on the receptacle, appendages have been developed; (I) apical zone of the receptacle, appendages on the right side, hyaline and darkened at the base, two symmetric perithecia are seen, the left one broken, a fusiform, highly hyaline ascospore is seen sideways in the formed opening; and (J) frontal view of the Holotype thallus, a. foot cell, b. receptacle, c. appendages, d. perithecia.
Figure 1. Peyritschiella styngeti, (A) dorsal view of the host Styngetus deyrollei Solsky [23]; (B) stylus of the host which was infected; (C) lateral view of the thallus on a seta from the stylus of the host; (D) apical zone of the perithecia, showing the four papillae, characteristic of the species; (E) antheridia, growing on the apical zone, besides the perithecia, growing apically on the appendages; (F) first stage of the growing thallus, growing on a seta from the stylus of the host, the foot cell has developed and the bottom cell of the ascospore has elongated, the darkened division between booth cells of the ascospore in a dark brown is visible, looking like a small cross, apical cell of the ascospore has not yet grown, the thallus has not developed, and the structures are highly hyaline; (G) thallus developing, foot cell has grown and the receptacle’s cells are developing, apical structures which include perithecia and appendages have not been fully developed; (H) growing thallus, upper level of the receptacle is developing, perithecia growing on the apical are of the receptacle, coloration has darkened on the receptacle, appendages have been developed; (I) apical zone of the receptacle, appendages on the right side, hyaline and darkened at the base, two symmetric perithecia are seen, the left one broken, a fusiform, highly hyaline ascospore is seen sideways in the formed opening; and (J) frontal view of the Holotype thallus, a. foot cell, b. receptacle, c. appendages, d. perithecia.
Taxonomy 05 00053 g001
Figure 2. Phase-contrast microscopy (PCM) of P. styngeti, (A) front view of the thalli. Melanized receptacle, two perithecia and margin developing, hence the evident asymmetry of the perithecia, appendages have yet to be seen from this view, asci visible inside the left perithecia; (B) frontal view of the thalli, appendages are developing on each side of the perithecia, which are lobulated in the apical zone, melanized receptacle overlapping looking almost as one-leveled, not fully developed, high pigmentation in both receptacle and foot cell; and (C) front view, not fully developed, perithecia with papillae containing asci, appendages starting to develop on each side of the perithecia, last row of cell of the receptacle also developing, receptacle and foot cell highly pigmented.
Figure 2. Phase-contrast microscopy (PCM) of P. styngeti, (A) front view of the thalli. Melanized receptacle, two perithecia and margin developing, hence the evident asymmetry of the perithecia, appendages have yet to be seen from this view, asci visible inside the left perithecia; (B) frontal view of the thalli, appendages are developing on each side of the perithecia, which are lobulated in the apical zone, melanized receptacle overlapping looking almost as one-leveled, not fully developed, high pigmentation in both receptacle and foot cell; and (C) front view, not fully developed, perithecia with papillae containing asci, appendages starting to develop on each side of the perithecia, last row of cell of the receptacle also developing, receptacle and foot cell highly pigmented.
Taxonomy 05 00053 g002
Figure 3. Optic Microscope view of P. styngeti’s perithecia, (A) left perithecia, ascospores visible; (B) right perithecia asci containing ascospores slightly visible; and (C,D) frontal view of ascospore, bicellular, septate, fusiform, highly hyaline, and covered with mucilage.
Figure 3. Optic Microscope view of P. styngeti’s perithecia, (A) left perithecia, ascospores visible; (B) right perithecia asci containing ascospores slightly visible; and (C,D) frontal view of ascospore, bicellular, septate, fusiform, highly hyaline, and covered with mucilage.
Taxonomy 05 00053 g003
Figure 4. Scanning electron microscopy (SEM) of P. styngeti, (A) young specimen of the thallus, only one perithecium has developed, the upper level of the receptacle is uneven because it has not developed fully, structures are seen; and (B) apical zone of the perithecium, showing the four papillae, diagnostic characteristic for the species.
Figure 4. Scanning electron microscopy (SEM) of P. styngeti, (A) young specimen of the thallus, only one perithecium has developed, the upper level of the receptacle is uneven because it has not developed fully, structures are seen; and (B) apical zone of the perithecium, showing the four papillae, diagnostic characteristic for the species.
Taxonomy 05 00053 g004
When compared with P. angolensis (Thaxt.) I.I. Tav. 1985 [18], P. styngeti presents the same dark-colored foot cell and two lobulated perithecia; however, the receptacle in P. angolensis exhibits three row of cells of the same width, overlapped, making it look symmetrical and a little bit flattened, only darkened at the margin and over the lower row of cells [21]. Meanwhile, the aforementioned one presents three rows of highly pigmented cells, giving it a one-leveled receptacle appearance, with the upper row being wider than the other two, surrounding the perithecia.
Peyritschiella exilis (Thaxt.) I.I. Tav. 1985 [18], unlike P. styngeti, presents two highly pigmented perithecia which are similar in size to the receptacle. This structure is divided into three highly differentiated levels, and the pigmentation is only observed on the basal area and the foot cell. Meanwhile, P. vulgata (Thaxt.) I.I. Tav. 1985 [18] exhibits a difference mostly because it presents three rows of cells, pigmented on the first row of the cell but not in the last two rows, and the appendages are constricted, with two terminal perithecia which have an appendiculate tip, the most prominent difference when compared with P. styngeti [21].
In the case of P. furcifera (Thaxt.) I.I. Tav. 1985 [18], it exhibits lesser-developed levels, similar to the ones in P. styngeti. Although the apical cells are bigger in comparison with the last taxon, they also do not possess any pigmentation on the apical area nor the foot cell, as well as appendages which are short and unicellular [24].
With P. australiensis (Thaxt.) I.I. Tav. 1985 [18], it is observed that the present pigmentation on the base and sides of the receptacle, as well as the appendages arranged at the sides and in between the apical perithecia, also has an appendiculated tip. Meanwhile, P. mexicana (Thaxt.) I.I. Tav. 1985 [18] has well-differentiated levels, with evident pigmentation only on the sides of the base of the receptacle, two appendiculate perithecia, and multicellular appendages arranged laterally and constricted, alongside the aforementioned genres, which are differentiated from P. styngeti because of the lack of an elongate margin under the perithecia, leaving the hem “bare” [24].
Peyritschiella madagascariensis (Thaxt.) I.I. Tav. 1985 [18], on the other hand, presents a pigmented receptacle with lateral projections that seem to be protecting the perithecia; however, these projections are long and separated from the receptacle, compared to P. styngeti. Moreover, it exhibits a slim receptacle with only one level and appendiculate perithecia [24].
Peyritschiella stingeti sp.nov. can be identified by a darkened foot cell, followed by a translucent cell as the base of the receptacle which is fully dark in color, forming a cone-shaped receptacle with an upper margin of transversal cells surrounding the base of the symmetrical perithecia, which only possesses two, which have an appendiculated tip with four cruciform papillae, and unicellular appendages at the sides of the perithecia, which are darkened at the base and fusiform bicellular ascospores, highly hyaline with a mucilage covering both cells.

4. Discussion

Peyritschiella is a genus that has been reported to be parasitic on rove beetles. In Mexico’s case, P. exilis has been cited over Belonuchus formosus Gravenhorst 1806 [25] (current valid name B. rufipennis Fabricius 1801) [26] and Philonthus oxyporinus Sharp 1885 [27] (current valid name B. oxyporinus Sharp 1885) [27], P. furcifera on Philonthus centralis Sharp 1885 [27], P. mexicana on Philonthus atriceps Sharp 1885 [27], P. princeps (Thaxt.) I.I. Tav. 1985 [18] on Philonthus sp. and Quediomacrus puniceipennis Solsky 1868 [28], and, finally, P. vulgata on Philonthus flavolimbatus Erichson 1840 [29]. Considering P. styngeti on Styngetus deyrollei, the taxonomic richness increases to six species.
In this study, 787 organisms of rove beetles were examined from different genera (Philonthus, Oligotergus, Platydracus and Chroaptomus), of which 476 were identified as Styngetus deyrollei. Among these, 104 were infected with thallus at different developmental stages, representing 22% of infected organisms in this species and 13.21% of all organisms revised.
The Staphylinidae family represents a group of arthropods highly parasitized by Laboulbeniales. Worldwide, there have been reported incidents of almost every family but Ceratomycetaceae; regardless, one important characteristic of this organism that needs to be highlighted is its specificity towards its hosts, which has made it clear for the fungi to be described as species-specific in most cases [18,30]. Frank [31] put Peyritschiella in the family Peyritschiellaceae as rove beetle parasites by excellence, before they were translated to their correct family, Laboulbeniaceae.
The number of rove beetles described worldwide goes up to 67,700 species; out of this, 1822 have been registered in Mexico, and 914 out of them are endemic to the territory [32]. These numbers make Mexico the country with the second-most diversity of rove beetles in Latin America [33], hence, considering that the genus Peyritschiella is frequent and presents specificity for this host, a high richness of species can be expected. So far, only the following 10 species of Laboulbeniales are known to grow on Staphylinidae: Cucujomyces bilateralis (R.K. Bnj.) W. Rossi & A. Weir 2008 [34], Corethromyces brasilianus Thaxt. 1900 [35], Laboulbenia cristata Thaxt. 1893 [15], L. philonthi Thaxt. 1893 [15], Mimeomyces quedionuchi Thaxt. 1931 [2], Peyritschiella exilis, P. furcifera, P. mexicana, P. princeps, and P. vulgata, [18,36], which represents only 12.34% of the 81 species known for the country, showing the necessity of maintaining mycological and entomological studies on those that are the most diverse organism groups.

5. Conclusions

Peyritschiella styngeti is a species found on the stylus of Styngetus deyrollei, predatory beetles that can be found between the leaf litter in tropical montane cloud forests. They are also distributed in Hidalgo, Puebla, San Luis Potosí, and Veracruz.
With this study, the number of Laboulbeniales species for Mexico goes up to 82, out of which 11 are parasitizing rove beetles. For the Peyritschiella genus, the number rises to 53 from the 52 previously known worldwide.
The studied species were obtained from specimens from an entomological collection, lent by the CC-UAEH, which highlights the importance of investigating recent biological collections, especially in the case of Laboulbeniales, which are a lesser-known group and possibly have a high level of diversity and endemism in Mexico.

Author Contributions

Conceptualization, E.L.O.-P., S.B.-H., and T.R.; methodology, E.L.O.-P., and S.B.-H.; validation, S.B.-H., E.L.O.-P., J.M., and J.A.; investigation, E.L.O.-P., S.B.-H.; resources, S.B.-H. and T.R.; data curation, E.L.O.-P.; writing—original draft preparation, E.L.O.-P.; writing—review and editing, E.L.O.-P., S.B.-H., T.R., J.M., and J.A.; visualization, S.B.-H., T.R., and E.L.O.-P.; supervision, S.B.-H., T.R., J.M., and J.A.; project administration, T.R. and S.B.-H.; funding acquisition, S.B.-H. and T.R. All authors have read and agreed to the published version of the manuscript.

Funding

This research was financed by the Instituto Politécnico Nacional under the project SIP20251281.

Data Availability Statement

All of the data that support the findings of this study are available in the main text and two appendices listed below.

Acknowledgments

We acknowledge the Instituto Politécnico Nacional for the financial support of this research. We thank the CC-UAEH (Universidad Autónoma del Estado de Hidalgo, México) for the materials to review and the taxonomic guidance during the species identifications, and all the extra resources provided regarding the hosts studied, to Berenit Mendoza Garfias for the scanning electron microscope (SEM) and the Phase-contrast microscopy (PCM) images (LANABIO, Instituto de Biología, UNAM), and last but not least, to the Mycology Laboratory, part of the Escuela Nacional de Ciencias Biológicas (ENCB), IPN, for the equipment and materials used during the research process. The authors have reviewed and edited the output and take full responsibility for the content of this publication.

Conflicts of Interest

The authors have declared that no competing interests exist.

Abbreviations

The following abbreviations are used in this manuscript:
CC-UAEHColeoptera Collection of Universidad Autónoma del Estado de Hidalgo
ENCBEscuela Nacional de Ciencias Biológicas (IPN)
IPNInstituto Politécnico Nacional

Appendix A

Table A1. Species of Laboulbeniales reported in Mexico (ordered alphabetically).
Table A1. Species of Laboulbeniales reported in Mexico (ordered alphabetically).
GenusHostThe Host’s FamilyVegetationReference
Order: Herpomycetales
Herpomyces paranensis Thaxt.BlaberaBlaberidae (Blattodea)Tropical Forest[1,13,14,15]
Herpomyces periplanetae Thaxt.PeriplanetaBlattidae (Blattodea)Tropical Forest[1,13,14,15]
Herpomyces platyzosteriae Thaxt.Platyzosteria ingens ScudderBlaberidae (Blattodea)Tropical Forest[1,13,14,15]
Order: Laboulbeniales
Ceratomyces ansatus Thaxt.TropisternusHydrophilidae (Coleoptera)Tropical forest
Temperate Forest
Boreal Forest
[1,13,14,15,18]
Ceratomyces confusus Thaxt.Tropisternus glaber Herbst
T. nimbatus Fabricius
Hydrophilidae (Coleoptera)Tropical Forest
Temperate Forest
Boreal Forest
[1,13,14,15,18]
Ceratomyces filiformis Thaxt.Tropisternus
Pleurohomus obscurus Sharp
Hydrophilidae (Coleoptera)
Dryopidae (Coleoptera)
Tropical Forest
Temperate Forest
Boreal Forest
[1,13,14,15]
Ceratomyces mexicanus Thaxt.Tropisternus nitidus Sharp
T. chalybeus Cast
Hydrophilidae (Coleoptera)Tropical Forest
Temperate Forest
Boreal Forest
[1,13,14,15,16]
Ceratomyces miriabilis Thaxt.Tropisternus
T. xantophus Sharp
Hydrophilidae (Coleoptera)Tropical Forest
Temperate Forest
Boreal Forest
[1,13,14,15]
Ceratomyces spiniger Thaxt.Tropisternus apicipalpis ChevrolatHydrophilidae (Coleoptera)Tropical Forest
Temperate Forest
Boreal Forest
[1,13,14,15,16]
Dimeromyces forficulae Thaxt.Doru lineare EschscholtzForficulidae (Dermaptera)Tropical Forest
Temperate Forest
Boreal Forest
[1,13,14,15,16]
Dimeromyces parasii Thaxt.ParasitusParasitidae (Mesostigmata)Tropical Forest
Temperate Forest
Boreal Forest
[1,13,14,15,16]
Dixomyces clivinae (Thaxt.) I.I. Tav.Clivina dentifermorata Putz
Clivina
Carabidae (Coleoptera)Tropical Forest
Temperate Forest
Boreal Forest
[1,13,14,15,16]
Dixomyces pallescens (Thaxt.) I.I. Tav.ClivinaCarabidae (Coleoptera)Tropical Forest
Temperate Forest
Boreal Forest
[16]
Eucantharomyces casnoniae Thaxt.Casnonia subdistincta ChaudoirCarabidae (Coleoptera)Tropical Forest
Temperate Forest
Boreal Forest
[1,13,14,15,16]
Eucantharomyces diaphorii Thaxt.Diaphorus tenuicornis ChaudoirCarabidae (Coleoptera)Tropical Forest
Temperate Forest
Boreal Forest
[1,13,14,15,16]
Homaromyces epieri R.K. Benj.UnespecifiedHisteridae (Coleoptera)Tropical Forest
Temperate Forest
Boreal Forest
[16]
Laboulbenia arietina Thaxt.DisonychiaCarabidae (Coleoptera)Tropical Forest
Temperate Forest
Boreal Forest
[1,13,14,15]
Laboulbenia armata Thaxt.Oedionychus sublineatus JacobyChrysomelidae (Coleoptera)Tropical Montane Cloud Forest[1,13,14,15]
Laboulbenia barbata Thaxt.Morion georgiae PalisotLeiodidae (Coleoptera)Tropical Montane Cloud Forest[1,13,14,15,16]
Laboulbenia brachini Thaxt.Brachinus elongatus Tourn
B. mexicanus Dejean
B. rhytiderus Chaudoir
Carabidae (Coleoptera)Tropical Forest
Temperate Forest
Boreal Forest
[1,13,14,15]
Laboulbenia bruchii (Speg.) Thaxt.Lema albini Kraatz
L. sallei Jacoby
L. dimidiaticornis Jacoby
Chrysomelidae (Coleoptera)Oak Forest
Pine Tree-Oak Forest
[1,13,14,15]
Laboulbenia catascopi Thaxt.Catoscopus
Pinacodera atrata Chevrolat
Coptodera arcuata Chevrolat
Colpodes auratus Chaudoir
Carabidae (Coleoptera)Tropical Forest
Temperate Forest
Boreal Forest
[1,13,14,15]
Laboulbenia decipiens Thaxt.Galerita nigra ChevrolatCarabidae (Coleoptera)Tropical Forest
Temperate Forest
Boreal Forest
[1,13,14,15]
Laboulbenia diabrotica Thaxt.Diabrotica fairmairei BalyChrysomelidae (Coleoptera)Tropical Forest
Temperate Forest
Boreal Forest
[1,13,14,15]
Laboulbenia disonichae Thaxt.Disonycha figurata JacobyChrysomelidae (Coleoptera)Tropical Forest
Temperate Forest
Boreal Forest
[1,13,14,15]
Laboulbenia egae Thaxt.EgaCarabidae (Coleoptera)Temperate Forest[1,13,14,15]
Laboulbenia elongata Thaxt.ColpodesCarabidae (Coleoptera)Tropical Forest
Temperate Forest
Coniferous Tree Forest
[1,13,14,15]
Laboulbenia erecta Thaxt.Colpodes agilis Chaudoir
C. evanescens Bates
Carabidae (Coleoptera)Tropical Forest
Temperate Forest
Coniferous Tree Forest
[1,13,14,15]
Laboulbenia flaccida Thaxt.Casonia subdistincta ChaudoirCarabidae (Coleoptera)Tropical Forest
Temperate Forest
Boreal Forest
[1,13,14,15]
Laboulbenia flagellata Peyr.Onypterigia pusilla ChaudoirCarabidae (Coleoptera)Tropical Forest
Temperate Forest
Boreal Forest
[1,13,14,15]
Laboulbenia galeritae Thaxt.Galerita forreri Bates
G. mexicana Chaudoir
Carabidae (Coleoptera)Tropical Forest
Temperate Forest
Boreal Forest
[1,13,14,15]
Laboulbenia guerinii Thaxt.Gyretes
G. boreandri Chevrolat
G. immarginatus Chevrolat
G. leionatus Duby
Gyrinidae (Coleoptera)Tropical Forest
Temperate Forest
[1,13,14,15]
Laboulbenia gyrinidarum Thaxt.GyrinusGyrinidae (Coleoptera)Tropical Forest
Temperate Forest
Boreal Forest
[1,13,14,15]
Laboulbenia homophoetae Speg.Asphaera transversofasciata Jacoby
Oedionychus sublineata Jacoby
Systema littera Linneus
Chrysomelidae (Coleoptera)Tropical Forest
Subtropical Forest
Temperate Forest
Deciduous Forest
[1,13,14,15]
Laboulbenia mexicana Thaxt.Galerita
G. mexicana Chaudoir
G. aequinoctialis Chaudoir
G. nigra Chevrolat
Carabidae (Coleoptera)Tropical Forest
Temperate Forest
Boreal Forest
[1,13,14,15]
Laboulbenia minima Thaxt.CallidaCarabidae (Coleoptera)Tropical Forest
Temperate Forest
Tropical Montane Cloud Forest
[1,13,14,15]
Laboulbenia morionis Thaxt.Morion georgiae Palisot
M. monillicornis Latreille
Moriosomus sylvestris Motschulsky
Carabidae (Coleoptera)Tropical Montane Cloud Forest[1,13,14,15,16]
Laboulbenia pachytelis Thaxt.Pachyteles mexicanus Chaudoir
P. longicornis Chaudoir
P. seriatoporus Chaudoir
Carabidae (Coleoptera)Tropical Forest
Temperate Forest
Tropical Montane Cloud Forest
[1,13,14,15]
Laboulbenia pallescens Thaxt.Clivina dilutipennis PutzcysCarabidae (Coleoptera)Tropical Forest
Temperate Forest
Boreal Forest
[1,13,14,15]
Laboulbenia parvula Thaxt.Pelmatellus obtusus BatesCarabidae (Coleoptera)Tropical Forest
Temperate Forest
Boreal Forest
Tropical Montane Cloud Forest
[1,13,14,15]
Laboulbenia pheropsophi Thaxt.Pheropsophus aequinoctialis Linnaeus
P. biplagiatus Chaudoir
Carabidae (Coleoptera)Tropical Forest
Temperate Forest
Boreal Forest
Tropical Montane Cloud Forest
[1,13,14,15]
Laboulbenia polyphaga Thaxt.Phlaeotheratus quadricollis Chaudoir
Stenognathus quadricollis Chaudoir
Carabidae (Coleoptera)Tropical Forest
Pine tree-Oak Forest
Tropical Montane Cloud Forest
[1,13,14,15]
Laboulbenia pygmaea Thaxt.GaleritaCarabidae (Coleoptera)Tropical Forest
Temperate Forest
Boreal Forest
[1,13,14,15]
Laboulbenia sbordonii W. Rossi & CesariMexaphaenops intermedius BarrCarabidae (Coleoptera)Temperate Forest
Coniferous Tree Forest
[10]
Laboulbenia texana Thaxt.Brachinus lateralis DejeanCarabidae (Coleoptera)Pine Tree-Oak Forest
Tropical Forest
[1,13,14,15]
Laboulbenia variabilis Thaxt.Poecilus mexicanus ChaudoirCarabidae (Coleoptera)Tropical Forest
Temperate Forest
Boreal Forest
[1,13,14,15]
Laboulbenia vulgaris Peyr.Bembidion mexicanum DejeanCarabidae (Coleoptera)Coniferous Tree Forest[1,13,14,15]
Limnaiomyces tropisterni Thaxt.TropisternusHydrophilidae (Coleoptera)Tropical Forest
Temperate Forest
Boreal Forest
[1,13,14,15]
Prolixandromyces corniculatus R.K. Benj.VeliaVeliidae (Hemiptera)Tropical Forest
Temperate Forest
Boreal Forest
[11,12]
Prolixandromyces veliae R.K. Benj.VeliaVeliidae (Hemiptera)Tropical Forest
Temperate Forest
Boreal Forest
[11,12,16]
Rhachomyces magrinii W. Rossi & M. LeonardiMexaphaenops elegans BarrCarabidae (Coleoptera)Temperate Forest
Coniferous Tree Forest
[19]
Rhachomyces mateui BalazucXendromius brachinoides MateuHydrophilidae (Coleoptera)Tropical Forest
Temperate Forest
Boreal Forest
[9,16]
Rhachomyces quetzalcoatl BalazucParatrechus mexicanus PutzcysCarabidae (Coleoptera)Coniferous Forest[9,16]
Rhachomyces velatus Thaxt.Gynandropus mexicanus Putzcys
Colpodes agilis Chaudoir
Carabidae (Coleoptera)Coniferous Forest
Tropical Forest
[1,13,14,15,16]
Rhachomyces zuphii Thaxt.Zuphioides mexicanum ChaudoirCarabidae (Coleoptera)Coniferous Forest[1,13,14,15,16]
Rhizopodomyces basifurcatus R.K. Benj.Hebrus sp.Hebridae (Hemiptera)Tropical Forest
Temperate Forest
Boreal Forest
[11,12,16]
Rhizopodomyces merragate Thaxt.Hebrus bilineatus ChampionHebridae (Hemiptera)Tropical Forest
Temperate Forest
Boreal Forest
[11,12,16]
Rhizopodomyces mexicanus R.K. Benj.Hebrus bilineatus ChampionHebridae (Hemiptera)Tropical Forest
Temperate Forest
Boreal Forest
[11,12,16]
Rhizopodomyces polhemi R.K. Benj.Hebrus sp.Hebridae (Hemiptera)Tropical Forest
Temperate Forest
Boreal Forest
[11,12,16]
Rickia apiculifera Thaxt.Chondrocephalus debilis Bates
Other unspecified species of passalids
Passalidae (Coleoptera)Coniferous Forest[1,13,14,15,16]
Rickia bifida Thaxt.Passalus
P. punctiger Lepeletier & Audinet-Serville
Passalidae (Coleoptera)Coniferous Forest[1,13,14,15,16]
Rickia furcata Thaxt.EuzerconEuzerconidae (Mesostigmata)Tropical Forest
Coniferous Forest
Deciduous Forest
[1,13,14,15,16]
Rickia parasiti Thaxt.ParasitusParasitidae (Mesostigmata)Tropical Forest
Temperate Forest
Boreal Forest
[1,13,14,15,16]
Rickia passalina Thaxt.Chondrocephalus debilis Bates
passalids
Passalidae (Coleoptera)Coniferous Forest[1,13,14,15,16]
Stigmatomyces benjaminii W. Rosii & A. WeirSpilochroa polita MallochHeleomyzidae (Diptera)Temperate Forest
Tropical Montane Cloud Forest
[17]
Stigmatomyces indentatus Thaxt.PsilopaVeliidae (Hemiptera)Coniferous Forest
Tropical Forest
Deciduous Forest
[1,13,14,15]
Stigmatomyces inflatus Thaxt.SapromyzaLauxaniidae (Diptera)Coniferous Forest
Tropical Forest
Deciduous Forest
[1,13,14,15]
Stigmatomyces limnophorae Thaxt.OnesiaCalliphoridae (Diptera)Pine Tree-Oak Forest
Tropical Forest
Deciduous Forest
[1,13,14,15]
Stigmatomyces limosinae Thaxt.LimosinaSphaeroceridae (Diptera)Pine Tree-Oak Forest
Tropical Forest
Deciduous Forest
[1,13,14,15]

Appendix B

Table A2. Laboulbeniales species reported parasitizing rove beetles of the family Staphylinidae in Mexico.
Table A2. Laboulbeniales species reported parasitizing rove beetles of the family Staphylinidae in Mexico.
SpeciesHostVegetationReference
Balazucia bilateralis R.K. Benj.Phloeonomus sp.Tropical Forest
Temperate Forest
Boreal Forest
[16]
Corethromyces brasilianus Thaxt.Cryptobium flohri Sharp
C. venustum Sharp
C. similipenne Bernhauer
Tropical Forest
Temperate Forest
Boreal Forest
[1,13,14,15,16]
Laboulbenia cristata Thaxt.Paederus sp.
P. erythroderus Erichson
Tropical Forest
Temperate Forest
Boreal Forest
[1,13,14,15]
Laboulbenia philonthi Thaxt.Philonthus incertus Solsky
P. furvus var. flohrii Sharp
Tropical Forest
Temperate Forest
Boreal Forest
Tropical Montane Cloud Forest
[1,13,14,15]
Mimeomyces quedionuchi Thaxt.Quedius sp.Deciduous Forest
Coniferous Forest
[16]
Peyritschiella exilis (Thaxt.) I.I. Tav.Belonuchus rufipennis Erichson
Belonuchus oxyporinus Sharp
Deciduous Forest
Tropical Montane Cloud Forest
[1,13,14,15,16]
Peyritschiella mexicana (Thaxt.) I.I. Tav.Philonthus atriceps SharpTropical Forest
Temperate Forest
Boreal Forest
Tropical Montane Cloud Forest
[1,13,14,15,16]
Peyritschiella princeps (Thaxt.) I.I. Tav.Philonthus sp.
Quediomacrus puniceipennis Solsky
Tropical Forest
Temperate Forest
Boreal Forest
Tropical Cloud Forest
[1,13,14,15,16]
Peyritschiella vulgata (Thaxt.) I.I. Tav.Philonthus flavolimbatus ErichsonTropical Forest
Temperate Forest
Boreal Forest
Tropical Cloud Forest
[1,13,14,15,16]
Sphaleromyces quedionuchi Thaxt.Quedionuchus impuctus SharpDeciduous Forest[1,13,14,15]
Peyritschiella styngeti (E.L. Ortiz-Pacheco, Raymundo, Baut.-Hern.)Styngetus deyrollei SolskyTropical Montane Cloud ForestThis paper

References

  1. Thaxter, R. On some North American species of Laboulbeniaceae. Proc. Am. Acad. Arts Sci. 1890, 25, 5–14. Available online: https://www.biodiversitylibrary.org/part/246995 (accessed on 10 July 2025). [CrossRef]
  2. Thaxter, R. Contribution Towards Monograph of the Laboulbeniaceae; Reimpresion 1971; Bibliotheca mycologica; J. Cramer: Lehre, Germany, 1971; pp. 1896–1931. [Google Scholar]
  3. Thaxter, R. Contribution towards a monograph of the Laboulbeniaceae, Part V. Proc. Mem. Amer. Acad. Arts Sci. 1931, 16, 1–435. [Google Scholar] [CrossRef]
  4. Healewaters, D.; Blackwell, M.; Pfister, D.H. Laboulbeniomycetes: Intimate fungal associates of arthropods. Annu. Rev. Entomol. 2021, 66, 257–276. [Google Scholar] [CrossRef]
  5. Van der Linde, E.J.; Rhong, I.H. New and interesting records of South African fungi. XV. Two new Laboulbeniales records from South Africa. Afr. J. Bot. 1997, 63, 109–110. [Google Scholar] [CrossRef]
  6. Santamaría, S. Los Laboulbeniales, un grupo enigmático de hongos parásitos de insectos. Lazarroa 2001, 22, 3–19. [Google Scholar]
  7. Lindroth, C.H. Notes on the ecology of Laboulbeniaceae infesting carabid beetles. Sven. Bot. Tidskr. 1948, 42, 34–41. [Google Scholar]
  8. Peyritsch, J. Über Vorkommen und Biologie von Laboulbeniaceen. Sitzungsber. Kaiserl. Akad. Wiss. Math. Naturiwss. Cl. Abt. 1875, 72, 377–385. [Google Scholar]
  9. Luna-Zendejas, H.; Pérez-Silva, E.; Reyes-Castillo, P. The Laboulbeniales of Mexico and a study on three new records of Rickia parasiting beetles (Passalidae). Rev. Mex. Mic. 1988, 4, 303–316. [Google Scholar]
  10. Cavara, F. Funghetti parassiti raccolti nella Repubblica Argentina dal Dr. Carlo Spegazzini. Malpighia 1899, 13, 177–193. [Google Scholar]
  11. Balazuc, J. Recherches sur les Laboulbeniomycetes. II. Description de cinq especes nouvelles de Rhachomyces, parasites de Coleoptères Carabiques. Rev. Mycol. 1973, 38, 218–227. [Google Scholar]
  12. Rossi, W.; Cesari, G. Laboulbeniales (Ascomycetes) parassite di Coleotteri cavernicoli del Messico. In Problemi Attuali di Scienza e di Cultura, Sezione Missioni ed Esplorazioni, Section 1; Accademia Nazionale dei Lincei: Rome, Italy, 1997; Volume 171, p. 373. [Google Scholar]
  13. Benjamin, R.K. Laboulbeniales on semiaquatic Hemiptera, III. Rhizopodomyces. Aliso 1979, 9, 379–409. [Google Scholar] [CrossRef]
  14. Benjamin, R.K. Laboulbeniales on semiaquatic Hemiptera, IV. Addenda to Prolixandromyces. Aliso 1981, 10, 1–17. [Google Scholar] [CrossRef]
  15. Thaxter, R. New species of Laboulbeniaceae from various localities. Proc. Am. Acad. Arts Sci. 1893, 10, 156–188. [Google Scholar] [CrossRef]
  16. Thaxter, R. Preliminary diagnoses of new species of Laboulbeniaceae, VI. Proc. Am. Acad. Arts Sci. 1905, 41, 303–318. [Google Scholar] [CrossRef]
  17. Thaxter, R. Laboulbeniales parasitic on Chrysomelidae. Proc. Am. Acad. Arts Sci. 1914, 50, 17–50. [Google Scholar] [CrossRef]
  18. Tavares, I.I. Laboulbeniales (Fungi, Ascomycota); Mycologia memoir No. 9. J. Cramer; The New York Botanical Garden: Braunschweig, Germany, 1985; 627p. [Google Scholar]
  19. Rossi, W.; Weir, A. New Species of Stigmatomyces from various continents. Mycologia 2007, 99, 139–143. [Google Scholar] [CrossRef]
  20. Kaishian, P.J. Insects and their Laboulbeniales (Ascomycota, Fungi) of Lake Eustis and Emeralda Marsh Conservation Area: A case study on urbanization and diversity. Ecol. Evol. 2021, 11, 16618–16633. [Google Scholar] [CrossRef]
  21. Jayawardena, R.S.; Hyde, K.D.; Wang, S.; Sun, Y.-R.; Suwannarach, N.; Sysouphanthong, P.; Abdel-Wahab, M.A.; Abdel-Aziz, F.A.; Abeywickrama, P.D.; Abreu, V.P.; et al. Fungal diversity notes 1512–1610: Taxonomic and phylogenetic contributions on genera and species of fungal taxa. Fungal Divers. 2023, 117, 1–272. [Google Scholar] [CrossRef]
  22. Index Fungorum. 2025. Available online: http://www.indexfungorum.org/Names/Names.asp (accessed on 14 July 2025).
  23. Solsky, S. Deux Staphylins nouveaux du Mexique. Hor. Ent. Ross. BHL 1866, 4, 314–316. [Google Scholar]
  24. Thaxter, R. Contribution towards a monograph of the Laboulbeniaceae. Part II. Mem. Amer. Acad. Arts Sci. 1908, 13, 217–469. [Google Scholar] [CrossRef]
  25. Gravenhorst, J.L.C. Monographia Coleopterorum Micropterorum; Typis Henrici Dieterich: Gottingae, Germany, 1806; pp. 1–236. [Google Scholar]
  26. Fabricius, J.C. Systema Eleutheratorum Secundum Ordines, Genera, Species: Adiectis Synonymis, Locis, Observationibus, Descriptionibus; Kiliae: Imprensis Bibliopolii Academici novi1801; Volume II, 687p. Available online: https://www.biodiversitylibrary.org/page/63318329 (accessed on 15 July 2025).
  27. Sharp, D. Biologia Centrali-Americana. Insecta. Coleoptera; R.H. Porter: London, UK, 1885; Volume I, Part 2: Staphylinidae; pp. 1–824. [Google Scholar]
  28. Solsky, S. Études sur les Staphylinides du Mexique. Hor. Ent. Ross 1868, 5, 3–112. [Google Scholar]
  29. Erichson, W.F. Genera et Species Staphylinorum Insectorum Coleopterorum Familiae; F.H. Morin: Berlin, Germany, 1840; pp. 401–954, pls. 1–5. [Google Scholar]
  30. Thaxter, R. Contribution towards a monograph of the Laboulbeniaceae. Mem. Amer. Acad. Arts Sci. 1895, 12, 187–429. Available online: https://www.jstor.org/stable/41550031 (accessed on 29 July 2025). [CrossRef]
  31. Frank, J.H. The Parasites of Staphylinidae (Coleoptera) are a Contribution Towards an Encyclopedia of the Staphylinidae; Encyclopedia of Staphylinidae. Bulletin Agricultural Experiment Stations; University of Florida: Gainesville, FL, USA, 1982; 118p. [Google Scholar]
  32. Newton, A.F. StaphBase. Offline database catalog. (Consulted August 2025).
  33. Navarrete-Heredia, J.L.; Newton, A.F. Biodiversidad de Staphylinidae (Insecta: Coleoptera) en México. Rev. Mex. Biodivers. 2014, 85 (Suppl. S1), S332–S338. [Google Scholar] [CrossRef]
  34. Rossi, W.; Weir, A. New species of Cucujomyces (Laboulbeniales) on Chilean Leiodidae. Aliso 2008, 26, 9–14. [Google Scholar] [CrossRef]
  35. Thaxter, R. Preliminary diagnoses of new species of Laboulbeniaceae. Proc. Amer. Acad. Arts Sci. 1900, 35, 429–442. [Google Scholar] [CrossRef]
  36. Navarrete-Heredia, J.L.; Newton, A.; Thayer, M.; Ashe, J.; Chandler, D. Guía Ilustrada para los Géneros de Staphylinidae (Coleoptera) de México; Universidad de Guadalajara y CONABIO: Guadalajara, Mexico, 2002; 401p. [Google Scholar]
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MDPI and ACS Style

Ortiz-Pacheco, E.L.; Raymundo, T.; Bautista-Hernández, S.; Márquez, J.; Asiain, J. A New Peyritschiella Species (Laboulbeniales, Ascomycota) on Staphylinidae (Coleoptera, Insecta) from the Tropical Montane Cloud Forest of Mexico. Taxonomy 2025, 5, 53. https://doi.org/10.3390/taxonomy5040053

AMA Style

Ortiz-Pacheco EL, Raymundo T, Bautista-Hernández S, Márquez J, Asiain J. A New Peyritschiella Species (Laboulbeniales, Ascomycota) on Staphylinidae (Coleoptera, Insecta) from the Tropical Montane Cloud Forest of Mexico. Taxonomy. 2025; 5(4):53. https://doi.org/10.3390/taxonomy5040053

Chicago/Turabian Style

Ortiz-Pacheco, Ericka Lorena, Tania Raymundo, Silvia Bautista-Hernández, Juan Márquez, and Julieta Asiain. 2025. "A New Peyritschiella Species (Laboulbeniales, Ascomycota) on Staphylinidae (Coleoptera, Insecta) from the Tropical Montane Cloud Forest of Mexico" Taxonomy 5, no. 4: 53. https://doi.org/10.3390/taxonomy5040053

APA Style

Ortiz-Pacheco, E. L., Raymundo, T., Bautista-Hernández, S., Márquez, J., & Asiain, J. (2025). A New Peyritschiella Species (Laboulbeniales, Ascomycota) on Staphylinidae (Coleoptera, Insecta) from the Tropical Montane Cloud Forest of Mexico. Taxonomy, 5(4), 53. https://doi.org/10.3390/taxonomy5040053

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