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Research Article
Uptaded checklist, historical overview and illustrated guide to the stygobiont Malacostraca (Arthropoda: Crustacea) species of Yucatan (Mexico)
expand article infoDorottya Angyal, Nuno Simões§|, Maite Mascaró§
‡ Universidad Nacional Autónoma de México, Sisal, Mexico
§ Laboratorio Nacional de Resiliencia Costera, Sisal, Mexico
| Texas A&M at Corpus Christi, Corpus Christi, United States of America
Open Access

Abstract

This study provides an updated checklist and an illustrated guide to the 17 currently known stygobiont Malacostraca species of the state of Yucatan (Yucatan Peninsula, Mexico). The compilation is based on the individuals collected during our cave-diving expeditions (2016–2019), and, has the purpose of expanding previous knowledge on the taxonomy of these subterranean crustaceans. The identification guide contains drawings of the main diagnostic characters of the species as well as a brief introduction of the relevant malacostracan orders. The information is further complemented with a historic account and timeline of the stygobiont Malacostraca species of the Yucatan Peninsula. This is the first study that provides a unified tool for the morphological identification of these highly endemic species.

Keywords

amphipods, decapods, groundwater, isopods, mysids, sinkholes, stygiomysids, thermosbaenaceans, Yucatan Peninsula

Introduction

The Yucatan Peninsula (southeastern Mexico) groundwater ecosystems harbour a highly endemic, crustacean-dominated fauna that present a variety of morphological and physiological adaptations to life in subterranean water environments (eg. Álvarez et al. 2008). Currently, 33 stygobiont (subterranean water-restricted) malacostracan species are known from the groundwater ecosystems of the Mexican federal states of the peninsula (eg. Álvarez et al. 2015; Angyal et al. 2020), which belong to six different orders (Decapoda: 14 sp., Amphipoda: 8 sp., Isopoda: 7 sp., Stygiomysida: 2 sp., Mysida: 1 sp., Thermosbaenacea: 1 sp.). All but three of the 33 species are endemic to the Yucatan Peninsula and half of them have bibliographically confirmed distribution records from the state of Yucatan. A timeline and historical data about the description of the groundwater-restricted Malacostraca of the Mexican states of the peninsula can be found in Table 1. The appearance of the species follows a chronological order, starting with the earliest species described and ending with the most recently discovered one.

Table 1.

Historical timeline and distribution data of the stygobiont Malacostraca species of the Yucatan Peninsula. Abbreviations: YUC = state of Yucatan; YP = Yucatan Peninsula; ROO = state of Quintana Roo; CAM = state of Campeche; COZ = Cozumel Island (in Quintana Roo); MNHB = Museum der Naturkunde für Humboldt Universität zu Berlin; UMLSA = University of Michigan Museum of Zoology, BMNH = British Museum (National History), London; USNM = National Museum of Natural History, Smithsonian Institution, Washington D.C.; CNCR UNAM = National Collection of Crustaceans, UNAM, Institute of Biology, Mexico City; ZMUA = Zoologisch Museum, University of Amsterdam. Distribution with an asterisk (for example COZ*) = the species is known only from its type locality.

Species Order Description Type locality Holotype Endemic in the YP Environment YP states distribution
Barbouria cubensis (von Martens, 1872) Decapoda von Martens 1872 Provincia de La Habana, Cuba MNHB No saline water ROO
Creaseriella anops (Creaser, 1936) Isopoda Creaser 1936 Cenote Sambulá (YUC) UMLSA Yes fresh and saline water YUC, ROO, CAM
Antromysis cenotensis Creaser, 1936 Mysida Creaser 1936 Grutas de Balancanché (YUC) UMLSA Yes fresh water YUC, ROO
Creaseria morleyi (Creaser, 1936) Decapoda Creaser 1936 Cueva de San Isidro (YUC) UMLSA Yes fresh water YUC, ROO, CAM
Typhlatya pearsei Creaser, 1936 Decapoda Creaser 1936 Grutas de Balancanché (YUC) UMLSA Yes fresh water YUC, ROO, CAM
Stygiomysis holthuisi (Gordon, 1958) Stygiomysida Gordon 1958 Devil’s Hole, St. Martin, Lesser Antilles (France) BMNH No fresh water YUC, ROO
Typhlatya mitchelli H.H.III Hobbs & H.H.Jr. Hobbs, 1976 Decapoda Hobbs and Hobbs 1976 Cenote Kabahchén (YUC) USNM Yes fresh water YUC, ROO
Typhlatya campecheae H.H.III Hobbs & H.H.Jr. Hobbs, 1976 Decapoda Hobbs and Hobbs 1976 Grutas de Xtacumbilxunaán (CAM) USNM Yes fresh water CAM
Mayaweckelia yucatanensis Holsinger, 1977 Amphipoda Holsinger 1977 Grutas de Xtacumbilxunaán (CAM) USNM Yes fresh water CAM*
Mayaweckelia cenoticola Holsinger, 1977 Amphipoda Holsinger 1977 Cenote Xtacabihá (YUC) USNM Yes fresh water YUC, ROO, CAM
Parhippolyte sterreri (C.W.J. Hart & Manning, 1981) Decapoda Hart and Manning 1981 Tucker’s Town Cave, Tucker’s Town, Bermuda USNM No saline water COZ
Metacirolana mayana (Bowman, 1987) Isopoda Bowman 1987 Cueva Quebrada (COZ) USNM Yes brakish and saline water ROO, COZ
Tulumella unidens Bowman & Iliffe, 1988 Thermosbae- nacea Bowman and Iliffe 1988 Cenote Naharon (ROO) USNM Yes brakish and saline water YUC, ROO
Yagerocaris cozumel Kensley, 1988 Decapoda Kensley 1988 Cenote Areolito (COZ) USNM Yes saline water ROO, COZ
Agostocaris bozanici Kensley, 1988 Decapoda Kensley 1988 Cenote Xcan-Ha (COZ) USNM Yes saline water COZ*
Tuluweckelia cernua Holsinger, 1990 Amphipoda Holsinger 1990 Cenote Calavera (ROO) USNM Yes brakish and fresh water YUC, ROO
Bahadzia bozanici Holsinger, 1992 Amphipoda Holsinger 1992 Cueva Quebrada (COZ) USNM Yes saline water ROO, COZ
Bahadzia setodactylus Holsinger, 1992 Amphipoda Holsinger 1992 Cenote Xcan-Ha (COZ) USNM Yes saline water COZ
Stygiomysis cokei Kallmeyer & Carpenter, 1996 Stygiomysida Kallmeyer and Carpenter 1996 Cenote Calavera (ROO) USNM Yes fresh and brakish water YUC, ROO
Calliasmata nohochi Escobar-Briones, Camacho & Alcocer, 1997 Decapoda Escobar-Briones et al. 1997 Crack House Cave, (ROO) CNCR UNAM Yes saline water ROO, COZ
Haptolana bowmani Botosaneanu & Iliffe, 1997 Isopoda Botosaneanu and Iliffe 1997 Grutas de Tzab-Nah (YUC) USNM Yes fresh water YUC
Yucatalana robustispina Botosaneanu & Iliffe, 1999 Isopoda Botosaneanu and Iliffe 1999 Cenote Papakal (YUC) ZMUA Yes fresh water YUC
Cirolana yunca (Botosaneanu & Iliffe, 2000) Isopoda Botosaneanu and Iliffe 2000 Cenote Sabak Ha (YUC) ZMUA Yes fresh water YUC
Cirolana yucatana Botosaneanu & Iliffe, 2000 Isopoda Botosaneanu and Iliffe 2000 Cenote Dzonotilá (YUC) ZMUA Yes fresh water YUC*
Procaris mexicana von Sternberg & Schotte, 2004 Decapoda Sternberg and Schotte 2004 Cueva Quebrada (COZ) USNM Yes saline water COZ
Typhlatya dzilamensis Álvarez, Iliffe & Villalobos, 2005 Decapoda Álvarez et al. 2005 Cenote Buya Uno (YUC) CNCR UNAM Yes saline water YUC, ROO
Triacanthoneus akumalensis Álvarez, Iliffe, Gonzalez & Villalobos, 2012 Decapoda Álvarez et al. 2012 Cenote Aak Kimin (ROO) CNCR UNAM Yes saline water ROO*
Hyalella cenotensis Marrón-Becerra, Hermoso-Salazar, Solís-Weiss, 2014 Amphipoda Marrón-Becerra el al. 2014 Cenote Aktun Ha (ROO) CNCR UNAM Yes fresh water ROO*
Cymadusa herrerae Ortiz & Winfield, 2015 Amphipoda Ortiz and Winifield 2015 Cenote Aerolito (COZ) CNCR UNAM Yes brakish water COZ*
Agostocaris zabaletai Mejía-Ortíz, Yañez & López-Mejía, 2017 Decapoda Mejía-Ortíz et al. 2017 Cenote Chempita (COZ) CNCR UNAM Yes saline water COZ
Anchialocaris paulini Mejía-Ortíz, Yañez & López-Mejía, 2017 Decapoda Mejía-Ortíz et al. 2017 Cenote Chempita (COZ) CNCR UNAM Yes saline water COZ*
Mayaweckelia troglomorpha Angyal, 2018 Amphipoda Angyal et al. 2018 Cenote Dzonbakal (YUC) CNCR UNAM Yes fresh water YUC
Curassanthura yucatanensis Álvarez, Benitez, Iliffe & Villalobos, 2019 Isopoda Álvarez et al. 2019 Cenote Nohoch Nah Chich (ROO) CNCR UNAM Yes fresh water YUC, ROO

Discovery of the first stygobiont malacostracan crustaceans in subterranean habitats of the state of Yucatan is dated back to the beginning of the twentieth century, when the Division of Historical Research of Carnegie Institution of Washington invited E. P. Creaser, F. G. Hall and A. S. Pearse to investigate the biology of the aquifers and subterranean ecosystems of Yucatan. In 1932, several ”cenotes” (water-filled sinkholes), ”aguadas” (shallow water-holes) and ”pozos” (karstic wells) were studied (Pearse 1936). Among other findings, this expedition resulted in the description of four subterranean malacostracan species new to science (Creaser, 1936). After a long hiatus, explorations were continued in the 1970’s, when J. R. Reddell and his colleagues (Texas Tech University) studied further cenotes and “grutas” (dry solution caves) of Quintana Roo, Campeche and Yucatan states (Reddell, 1977), resulting in the description of, among others, two stygobiont amphipod and decapod species (Hobbs and Hobbs 1976; Holsinger 1977). Cave diving expeditions in cenotes and the associated submerged cave passages of the peninsula began in the 1980’s. By the early 2000’s, more than ten subterranean malacostracan species had been described from the orders Thermosbaenacea, Stygiomysida, Isopoda and Amphipoda (eg. Bowman and Iliffe 1988; Holsinger 1990; Bowman and Iliffe 1999; Álvarez et al. 2005).

In 2016, the research group “Cenoteando” (www.cenoteando.com), of the Unidad Multidisciplinaria de Docencia e Investigación of the Facultad de Ciencias, Universidad Nacional Autónoma de México in Sisal (UNAM UMDI-Sisal), began their systematic studies of the biodiversity mapping, ecology and taxonomy of the cenote ecosystems in the state of Yucatan. Prior to Cenoteado’s work only less than five percent had been zoologically investigated out of the more than 3,000 officially registered cenotes in Yucatan (SDS Yucatan census). The project’s goal has been to provide data from cenotes that had never been studied, with expeditions leading to the discovery of stygobionts previously unknown in the region and to the description of species new to science (Angyal et al. 2018; Grego et al. 2019). Together with these records and the most recent description of Álvarez et al. (2019) of a new subterranean isopod, the number of stygobiont malacostracan species of the state of Yucatan has elevated to seventeen.

In the absence of a unified taxonomic guide, up to now, the identification of these species was possible only by a thorough knowledge of the original descriptions and other relevant literature on the species’ distribution and morphology. In order to facilitate further research of these rare, endemic species, the aim of this paper is to provide an updated checklist accompanied by an illustrated identification guide and a chronological historical account of the stygobiont malacostracan crustaceans of the state of Yucatan.

Materials and methods

Samples of malacostracan species were collected in 32 cenotes and submerged caves in the state of Yucatan between 2016 and 2019, during SCUBA cave-diving expeditions in the following municipalities: Abala, Cacalchen, Chochola, Chunchumil, Dzilam de Bravo, Ekmul, Homun, Huhi, Kopoma, Sotuta, Tecoh, Tixkakal, Tixkokob and Uman. Detailed information about the localities and the collected material can be found in Angyal et al. 2020 (https://zookeys.pensoft.net/article/47694/). The collected material was deposited in the Yucatán Colección de Crustáceos of the UNAM UMDI-Sisal, the Colección Nacional de Crustáceos, Instituto de Biología of the UNAM, Mexico City, and in the Collection of Crustaceans of the Hungarian Natural History Museum (HNHM), Budapest. Individuals were examined with a Nikon SM Z800 stereomicroscope. Thermosbaenaceans, stygiomysids, mysids and amphipods were dissected on slides and were observed with compound light microscope. For this, specimens were cooked in 10% KOH solution, rinsed with HCl and washed in distilled water. Cleared exoskeletons were stained with chlorazol black in glycerol, and then dissected in glycerol gelatin using stereomicroscope (Fišer et al. 2009). Photographs of diagnostic characters were made using an OMAX 14 OMP digital USB microscope camera. Line drawings were made after the collected material, based on (i) slide preparations and intact individuals using drawing tubes mounted in a Leica DM 1000 compound microscope and in a Leica M125 stereomicroscope, respectively, (ii) and on photographs. In the case of three isopod species (Haptolana bowmani, Cirolana yucatana and Curassanthura yucatanensis) which we were not able to collect, we relied solely on the illustrations of the original species descriptions. The drawings were edited graphically via computer, to ensure homogeneity of lines and shades. Species identification and creation of the identification guide were performed with the aid of the literature listed in Table 2.

Table 2.

List of references of the corresponding taxa used for the compilation of the illustrated identification guide.

Reference Corresponding taxon Reference Corresponding taxon
Álvarez et al. 2005 Typhlatya dzilamensis Hobbs and Hobbs 1976 Typhlatya mitchelli
Álvarez et al. 2019 Curassanthura yucatanensis Hobbs et al. 1977 genus Typhlatya
Angyal et al. 2018 Mayaweckelia troglomorpha Hobbs 1979 genus Typhlatya
Botosaneanu and Iliffe 1997 Haptolana bowmani Holsinger 1977 Mayaweckelia cenoticola
Botosaneanu and Iliffe 1999 Yucatalana robustispina Holsinger 1990 Tuluweckelia cernua
Botosaneanu and Iliffe 2000 Cirolana yunca, Cirolana yucatana Holthuis 1950 family Palaemonidae
Botosaneanu and Iliffe 2002 family Cirolanidae Horwitz et al. 1995 class Malacostraca
Botosaneanu and Iliffe 2006 family Cirolanidae Kallmayer and Carpenter 1996 Stygiomysis cokei
Bowman 1966 family Cirolanidae Kensley 1981 genus Curassanthura
Bowman 1977 genus Antromysis Lowry and Myers 2013 suborder Senticaudata
Bowman and Iliffe 1988 Tulumella unidens Meland et al. 2015 orders Mysida and Stygiomysida
Bowman et al. 1984 genus Stygiomysis Melic 2015 order Thermosbaenacea
Bruce 1986 family Cirolanidae Pérez-Aranda 1983a Typhlatya pearsei
Bruce 2008 family Cirolanidae Pérez-Aranda 1983b Creaseria morleyi
Bruce and Humphreys 1993 family Cirolanidae Pérez-Aranda 1984a Typhlatya mitchelli
Bruce et al. 2017 family Cirolanidae Pérez-Aranda 1984b Creaseriella anops
Brusca et al. 1995 family Cirolanidae Poore 2001 family Cirolanidae
Caroli 1937 family Cirolanidae Rioja 1953 family Cirolanidae
Creaser 1936 Antromysis cenotensis, Creaseriella anops, Creaseria morleyi, Typhlatya pearsei Tinnizi and Quddusi 1993 class Malacostraca
De la Fuente 1994 class Malacostraca Wagner 1994 order Thermosbaenacea
Gordon 1960 Stygiomysis holthuisi

Results

Updated checklist of the stygobiont Malacostraca of the state of Yucatan

Table 3 contains an updated checklist of the seventeen stygobiont malacostracan crustacean species that have been described to date from the state of Yucatan (12 species), or else, have bibliographically confirmed distribution records from the state up to september 2020 and were described elsewhere (5 species).

Table 3.

Checklist of the stygobiont malacostracan species of the state of Yucatan, with data on their distribution. Abbreviations: YUC = state of Yucatan, YP = Yucatan Peninsula, ROO = state of Quintana Roo, CAM = state of Campeche. Species with an asterisk (*) = the species was discovered and described from cenotes of YUC.

Superorder Order Family Genus Species valid name Original name Published distribution
Thermosbaenacea Tulumellidae Tulumella Tulumella unidens Bowman & Iliffe, 1988 Tulumella unidens Less than 20 cenotes and caves in YUC and ROO.
Stygiomysida Stygiomysidae Stygiomysis Stygiomysis holthuisi (Gordon, 1958) Rhopalonurus holthuisi Anguilla, Bahamas, Lesser Antilles (France), Puerto Rico. From the YP: less than 30 cenotes and caves in YUC and ROO.
Stygiomysis cokei Kallmeyer & Carpenter, 1996 Stygiomysis cokei Less than 20 cenotes and caves in YUC and ROO.
Mysida Mysidae Antromysis Antromysis cenotensis Creaser, 1936* Antromysis cenotensis Widely distributed in the central and northern parts of the YP, known from several wells, cenotes and caves in YUC and ROO.
Leptanthuridae Curasshantura Curassanthura yucatanensis Álvarez, Benítez, Iliffe & Villalobos, 2019 Curassanthura yucatanensis Cenote Nohoch Nah Chich (ROO), Cenote Chen Ha (YUC), Cenote Dzonotilá (YUC)
Peracarida Isopoda Cirolanidae Cirolana Cirolana yunca (Botosaneanu & Iliffe, 2000)* Haptolana yunca Cenotes Sabak Ha, Tres Oches, X’baba, Chihuo Hol (all in YUC)
Cirolana yucatana Botosaneanu & Iliffe, 2000* Cirolana (Anopsilana) yucatana Cenote Dzonotilá (YUC)
Creaseriella Creaseriella anops (Creaser, 1936)* Cirolana anops Known from numerous caves and cenotes in YUC and ROO, and a well in CAM.
Haptolana Haptolana bowmani Botosaneanu & Iliffe, 1997* Haptolana bowmani Grutas de Tzab-Nah, Cenotes Kambul, Mucuyché and Yuncú (all in YUC)
Yucatalana Yucatalana robustispina Botosaneanu & Iliffe, 1999* Yucatalana robustispina Less than 20 cenotes and caves in YUC.
Amphipoda Hadziidae Mayaweckelia Mayaweckelia cenoticola Holsinger, 1977* Mayaweckelia cenoticola Less than 20 cenotes and caves in YUC, ROO and CAM.
Mayaweckelia troglomorpha Angyal, 2018* Mayaweckelia troglomorpha Less than 20 cenotes and caves in YUC.
Tuluweckelia Tuluweckelia cernua Holsinger, 1990 Tuluweckelia cernua Some cenotes and caves in Yucatan and Quintana Roo.
Eucarida Decapoda Atydae Typhlatya Typhlatya pearsei Creaser, 1936* Typhlatya pearsei Widely distributed in cenotes and caves in YUC, ROO and CAM.
Typhlatya mitchelli H.H.III Hobbs & H.H.Jr. Hobbs, 1976* Typhlatya mitchelli Widely distributed in cenotes and caves in YUC and ROO.
Typhlatya dzilamensis Álvarez, Iliffe & Villalobos, 2005* Typhlatya dzilamensis Less than 20 cenotes and caves in YUC and ROO.
Palaemonidae Creaseria Creaseria morleyi (Creaser, 1936)* Palaemon morleyi Widely distributed in cenotes and caves in YUC, ROO and CAM.

Illustrated guide to the stygobiont Malacostraca species of Yucatan with the introduction of the orders

Order: THERMOSBAENACEA Monod, 1927

Figure 1

Antenna 1 biramous, antenna 2 uniramous. Mandibular palp present. Carapace short, forming dorsal brood pouch in females. Thoracic legs reduced, mostly two-branched. Gills lacking. Pleopods reduced or lacking.

Figure 1. 

Thermosbaenacea, schematic drawing.

Family: Tulumellidae Wagner, 1994

Tulumella unidens Bowman & Iliffe, 1988

Body length up to 3.5 mm of both gender. Antennula with scale (exopod) (Fig. 2A). Carapace covering pereonites 1–6, dorsally enlarged in ovigerous females (Fig. 2A). Pereopod I biramous, endopod five-segmented. Pereopods II-VII biramous, with two-segmented exopod and six-segmented endopod (Fig. 2B).

Figure 2. 

A Tulumella unidens habitus simplified drawing B T. unidens pereopod VI.

Order: STYGIOMYSIDA Caroli, 1937

Figure 3

Body elongated, vermiform. Second thoracopods are enlarged, dactylus and nail bend down to form a subchelate gnathopod. Both male and female pleopods are reduced to comprise a sympod/protopod, a one-segmented endopod and three-segmented exopod.

Figure 3. 

Stygiomysida, schematic drawing.

Family: Stygiomysidae Caroli, 1937

Stygiomysis holthuisi (Gordon, 1958)

Body length up to 9 mm of both gender. Body rather vermiform, carapace reduced. Pereopods 1–3 prehensile. Telson only slightly longer than wide at base; posterior margin with 15 spines in 5 groups, 1st, middle and 5th groups consist of strong, long spines (Fig. 4A). Uropod protopodal process with five long spines on apical margin and with several spines along the distal half of medial margin (Fig. 4B).

Figure 4. 

A Stygiomysis holthuisi telson B S. holthuisi uropod protopodal process.

Stygiomysis cokei Kallmeyer & Carpenter, 1996

Body length up to 15 mm of males and 22 mm of females. Body rather vermiform, carapace housing mouthparts and anterior three pairs of pereopods (Fig. 5A). Telson 1.7–2.0× longer than wide at base; posterior margin with 15–16 spines in five groups (Fig. 5B). Uropod slightly shorter than telson; protopodal process with seven or eight spines along medial and apical margins (Fig. 5C).

Figure 5. 

A Stygiomysis cokei carapace with appendages B S. cokei telson C S. cokei uropod protopodal process.

Order: MYSIDA Boas, 1883

Figure 6

The eight thoracic segments are covered by the carapace which is attached only to the first three. First two thoracic segments bear maxilliped, other six pairs of thoracic appendages are biramous perepoods. Ventral brood pouch enclosed by large, flexible oostegites present on females. Fourth pleopod longer than others in males and has a specialized reproductory function. Statocysts on uropods present.

Figure 6. 

Mysida, schematic drawing.

Family: Mysidae Haworth, 1825

Antromysis cenotensis Creaser, 1936

Body length up to 4.5 mm of both gender. Antenna 2 scale is about 4–4.5 times as long as wide, two-segmented (Fig. 7A). Telson nearly as long as wide at base, gradually narrowing posteriorly, armed with robust spine at each corner and one or two short spine in center (Fig. 7B). Inner ramus of uropod with static organ on basal half (Fig. 7C).

Figure 7. 

A Antromysis cenotensis scale of antenna 2 B A. cenotensis telson C A. cenotensis uropod with statocyst.

Order: ISOPODA Latreille, 1817

Figure 8

Body cylindrical or depressed dorsoventrally. Thorax of seven somites (peraeon), each somite bearing a pair of uniramous appendages, coxa bearing side-plates. First pair of thoracic appendages often subchelate, remaining thoracic appendages similar in structure. Abdomen of six somites (pleon), pleotelson present. Pleon bears five pairs of pleopods and one pair of uropod. Gills are on pleopods.

Figure 8. 

Isopoda, schematic drawing.

Family: Leptanthuridae Poore, 2001

Curassanthura yucatanensis Álvarez, Benítez, Iliffe & Villalobos, 2019

Body length up to 9 mm of females. Body slender, elongated (Fig. 9A). Head wider than long (Fig. 9A). Propodus palmar margins of pereopod I with 30 spines (Fig. 9B). Pereopods II-VI similar, much narrower than long (Fig. 9A). Pereopod VII lacking (Fig. 9A). Posterior margin of pleonite 6 rounded (Fig. 9C).

Figure 9. 

A Curassanthura yucatanensis habitus B C. yucatanensis propodus of pereopod I C C. yucatanensis pleonites. Drawings were adatpted from Álvarez et al. 2019.

Family: Cirolanidae Dana, 1852

Cirolana yunca (Botosaneanu & Iliffe, 2000)

Body length up to 10 mm of females. Body margins only slightly convex. Cephalon more than twice longer than maximal length, posterior margine deeply depressed (Fig. 10A). Rostrum small and blunt ending in dorsal view (Fig. 10A). Additional nails present on propodi of pereopods: one long, slightly curved blunt ending, and one short, conical (Fig. 10B). Uropodal exopodite slightly shorter than endopodite (Fig. 10C). Pleotelson with length equaling its width at the base (Fig. 10C).

Figure 10. 

A Cirolana yunca cephalon with rostrum B C. yunca nails of pereopod III dactylus (adapted from Botosaneanu & Iliffe 2000) C C. yunca pleotelson and uropods.

Cirolana yucatana (Botosaneanu & Iliffe, 2000)

Body length up to 6 mm of females. Body rather strongly widened in the middle. Cephalon large, strongly vaulted anteriorly, posterior margin slightly depressed (Fig. 11A). Rostrum small, triangular (Fig. 11A). Pereopods only with few spines (Fig. 11B). Uropods exopodite shorter and slender than endopodite, but rather thick-set (Fig. 11C). Pleotelson maximum width only slightly exceeding maximum length (Fig. 11C).

Figure 11. 

A Cirolana yucatana cephalon B C. yucatana pereopod II C C. yucatana pleotelson and uropods. Drawings were adapted from Botosaneanu & Iliffe 2000.

Creaseriella anops (Creaser, 1936)

Body length up to 23 mm of both gender. Able to roll into a ball (Fig. 12A). Cephalon oblong, twice as wide as long; posterior margin slightly concave (Fig. 12B). Pleotelson wider than long, along the distal margin several very short setae (Fig. 12C). Uropodal exopodite slightly shorter than endopodite; endo- and exopodite with row of very short setae on external margin and apex (Fig. 12C).

Figure 12. 

A Creaseriella anops rolled position B C. anops cephalon C C. anops pleotelson and uropods.

Haptolana bowmani Botosaneanu & Iliffe, 1997

Body length up to 7.5 mm of males and 9.5 mm of females. Body slender, cephalon having the shape of a helmet, wider than long, rostrum narrowly triangular (Fig. 13A). All pereopods clearly prehensile, with robust propodus, pereopods II-VII very spinose (Fig. 13B). Pereopods VI and VII distinctly longer than I-V. Uropods exopodite distinctly shorter than endopodite (Fig. 13C). Pleotelson longer than wide (Fig. 13C).

Figure 13. 

A Haptolana bowmani cephalon with rostrum B H. bowmani pereopod III C H. bowmani pleotelson and uropods. Drawings were adapted from Botosaneanu & Iliffe 1997.

Yucatalana robustispina Botosaneanu & Iliffe, 1999

Body length up to 4.5 mm of both gender. Cephalon with round lateral bulges and well developed triangular rostrum (Fig. 14A). Pereopod I with very long spines with particular structure on propod (2 spines), carpus (1 spine) and merus (1 spine) (Fig. 14B). Pleotelson subtrapezoidal (Fig. 14C). Uropodal exopodite with spines along external margin (Fig. 14C).

Figure 14. 

A Yucatalana robustispina cephalon with rostrum B Y. robustispina pereopod I C Y. robustispina pleotelson and uropods.

Order: AMPHIPODA Latreille, 1816

Figure 15

Body laterally compressed, slightly arched. Thorax of seven somites (peraeon), each segment bearing uniramous appendages, coxae bearing side-plates. Appendages of the first two thoracic somites modified as gnathopods. Abdomen six-segmented, abdominal somites 1–3 with large pleopods. Last three somites bear uropods, pleotelson absent. Gills at the inner base of pereopods.

Figure 15. 

Amphipoda, schematic drawing.

Family: Hadziidae Karman, 1943

Mayaweckelia cenoticola Holsinger, 1977

Body length up to 4 mm of males and 5.5 mm of females. Antenna 1 as long as, or a little longer than body, primary flagellum with 37–41 segments. Propodus of gnathopod 1 narrow, palm without distally notched spine teeth (Fig. 16A). Carpus of gnathopod 1 slightly longer than propodus (Fig. 16A). Pereopod VI and VII 60% of body length. Epimeral plates ventro-posterior corner not acuminate (Fig. 16B).

Figure 16. 

A Mayaweckelia cenoticola propodus of gnathopod 1 (Ish = ischium, Mer = merus, Car = carpus, Pr = propodus) B M. cenoticola epimeral plates 1-3 (Ep = epimeral plates).

Mayaweckelia troglomorpha Angyal, 2018

Body length up to 10 mm of both gender. Antenna 1 almost twice as long as body, primary flagellum with more than 60 articles. Propodus of gnathopod 1 less narrow, distally notched spine teeth present on palm (Fig. 17A). Carpus of gnathopod 1 1.5–1.7 times longer than propodus (Fig. 17B). Pereopod VI and VII 130% of body length. Epimeral plates ventro-posterior corner more distinct (Fig. 17C).

Figure 17. 

A Mayaweckelia troglomorpha notched spine teeth of gnathopod 1 propodus B M. troglomorpha gnathopod 1 schematic drawing (Ish = ischium, Mer = merus, Car = carpus, Pr = propodus) C M. troglomorpha epimeral plates 1-3 (Ep = epimeral plates).

Tuluweckelia cernua Holsinger, 1990

Anterior body region bend markedly downward (Fig. 18A). Body length up to 7 mm of males and 10 mm of females. Antenna 1 reaches at least 75% of body length. Gnathopod 2 propod long and relatively narrow (Fig. 18B). Uropod III proportionally long to body size, rami narrow, outer ramus of outer margin with small spines but lacking setae (Fig. 18C).

Figure 18. 

A Tuluweckelia cernua anterior body part B T. cernua gnathopod 2, schematic drawing (Mer = merus, Car = carpus, Pr = propodus, C = coxa) C T. cernua uropod III.

Order: DECAPODA Latreille,1802

Figure 19

First 3 pairs of thoracopods transformed on maxillipeds. First pair of pereopods usually bears chelae. Gills are usually enclosed by carapace’ folds. One pair of uropods is expanded and together with telson form caudal fin.

Figure 19. 

Decapoda, schematic drawing.

Family: Atydae De Haan, 1849

Typhlatya pearsei Creaser, 1936

Body length up to 19 mm of both gender. Rostrum extending anteriorly to at least midlength of second podomere of antennular peduncle (Fig. 20A). Exopod of pereopod V reduced, shorter than total length of basipodite (Fig. 20B).

Figure 20. 

A Typhlatya pearsei rostrum and eyestalk B T. pearsei pereopod V schematic drawing.

Typhlatya mitchelli Hobbs & Hobbs, 1976

Body length up to 22 mm of both gender. Rostrum not extending anteriorly beyond eyes (Fig. 21A). Exosceleton sometimes with pigmentation pattern (Fig. 21A). Ratio of carpus/propodus of pereopod II is more than 2.5 (Fig. 21B). Exopod of pereopod V reaching at least distal extremity of basis and often as far as proximal 5th of merus (Fig. 21C).

Figure 21. 

A Typhlatya mitchelli rostrum and eyestalks B T. mitchelli pereopod II schematic drawing C T. mitchelli pereopod V schematic drawing.

Typhlatya dzilamensis Álvarez, Iliffe & Villalobos, 2005

Body length up to 24 mm of both gender. Rostrum unarmed, anteriorly oriented, reaching distal margin of eyes, triangular in dorsal view (Fig. 22A). Ishium and merus of pereopod III-V fused (Fig. 22B). Pleura of second abdominal somite with ventral margin not bilobed (Fig. 22C).

Figure 22. 

A Typhlatya dzilamensis rostrum and eyestalks B T. dzilamensis pereopod III schematic drawing C T. dzilamensis carapace and abdomen schematic drawing.

Family: Paleomonidae Rafinesque, 1815

Creaseria morleyi (Creaser, 1936)

Body length up to 42 mm of both gender. Rostrum with dorsal and ventral teeth (Fig. 23A). Telson with two-two short spines on distal half, apex with strong spines on both side and some long, fine setae in center (Fig. 23B).

Figure 23. 

A Creaseria morleyi rostrum and eyestalks B C. morleyi telson and uropods.

Discussion

One third of the stygobiont Malacostraca fauna of the Yucatan Peninsula has been discovered in the last 20 years, showing an increasing interest of biodiversity surveys in underwater ecosystems in this region. Half of the currently known species were described from the state of Quintana Roo, partly due to the intensive diving explorations of the Nohoch Nah Chich and Sac Actun submerged cave systems conducted since the late eighties (Álvarez et al. 2015). The diversity of the stygofauna of the anchialine caves of Cozumel Island (Quintana Roo) is remarkable: nine malacostracan species have been discovered in the island in the last three decades (e.g. Bowman 1987; Mejía-Ortíz et al. 2017; Ortiz and Winfield, 2015). Only twelve of the stygobiont malacostracan species of the peninsula have been described from the state of Yucatan, but five additional species have distribution data from this state (Angyal et al. 2020). New discoveries of recent years indicate the need of further subterranean biological explorations to gain deeper knowledge on the species richness and distribution of these cryptic habitats of Yucatan (e.g. Angyal et al. 2018; Álvarez et al. 2019).

The taxonomic status of five species of the presented checklist has been changed since the original descriptions. Creaseriella anops was originally described as Cirolana anops Creaser, 1936. In a thorough taxonomic revision of cirolanid isopods from Mexico, Rioja (1953) considered necessary to establish a new monotypic genus: Creaseriella Rioja, 1953, of which Creaseriella anops (Creaser, 1936) was the type species.

Fourteen years after the discovery of the new paleomonid shrimp Paleomon morleyi Creaser, 1936, a new genus, Creaseria Holthuis, 1950 was established, of which Creaseria morleyi (Creaser, 1936) is the type species by monotypy (Holthuis 1950).

Two years after its discovery, the stygiomysid Rhopalonurus holthuisi Gordon, 1958 had been reallocated to the genus Stygiomysis by Gordon (1960), as Stygiomysis holthuisi (Gordon, 1958).

The cirolanid isopod Cirolana yunca was originally described as Haptolana yunca Botosaneanu & Iliffe, 2000. More recently, however, the species has been reallocated to the widely distributed genus Cirolana by Bruce (2008).

Eight years after the discovery of the isopod Cirolana (Anopsilana) yucatana Botosaneanu & Iliffe, 2000, Boyko et al. (2008) considered the subgenus Anopsilana Paulin & Delamare Deboutteville, 1956 to be the junior synonym of the genus Cirolana Leach, 1818, therefore the current valid combination of the species is Cirolana yucatana (Botosaneanu & Iliffe, 2000).

There are four monotypic, highly endemic genera (Tuluweckelia Holsinger, 1990; Creaseriella Rioja, 1953; Yucatalana Botosaeanu & Iliffe, 1999; Creaseria Holthuis, 1950) known from subterranean waters of Yucatan. The other eight genera presented in the updated checklist have more than one species and have a wider distribution range, as follows.

Apart from Tulumella unidens, there are two other species of the genus Tulumella Bowman & Iliffe, 1988, described from anchialine caves of the Bahamas (Yager 1988).

Currently, the genus Stygiomysis Caroli, 1937 contains five species from the Dominican Republic, the Caicos Island, Cuba, Jamaica and Italy (Bowman et al. 1984). There are two described species of the genus within the Yucatan Peninsula.

Further species of the genus Antromysis Creaser, 1936 are known from Suriname, The Bahamas, Jamaica, Costa Rica and Cuba. The second species discovered of the genus Antromysis in Mexico was Antromysis reddelli Bowman 1977 from Cueva de las Maravillas in Oaxaca (Bowman 1977).

The genus Curassanthura Kensley, 1981 consists five species. The four previously known species are from Caribbean and North Atlantic islands. C. yucatanensis is the first Curassanthura species to be described from a continental environment (Poore 2009; Álvarez et al. 2019).

The isopod Cirolana Leach, 1818 is a widely distributed genus with more than 200 species worldwide.

Currently, there are five more valid species of the genus Haptolana Bowman, 1966, known from subterranean waters of Belize, Cuba, Somalia, and Western Australia. H. bowmani is the only species reported from Mexico.

The genus Mayaweckelia Holsinger, 1977 consists of three species. Validity of the third species, M. yucatanensis Holsinger, 1977, known from a single locality in Campeche is questionable, as the author points out that „the original description was based on what appear to be submature specimens, therefore raising the strong possibility that the differences noted between M. yucatanensis and M. cenoticola are due primarly to age” (Holsinger 1990).

The currently known seventeen valid species of the genus Typhlatya are characterized by a disjunct distribution around the Caribbean (Yucatan Peninsula, Cuba, Honduras, Bermuda, The Bahamas and the United States of America), in Europe (France and Spain) and the Galapagos and Ascension Islands, which makes this genus an interesting group to test biogeographical hypotheses (Álvarez et al. 2005; Espinasa et al. 2019; Chávez-Solís et al. 2020). Currently, there are four described species of this genus within the Yucatan Peninsula.

Conclusions

Subterranean habitats of Yucatan are characterized by a remarkable diversity of highly adapted, narrowly distributed crustacean species. Seventeen out of the 33 groundwater-restricted malacostracan species of the peninsula are currently known from waterfilled sinkoles (cenotes) and the associated submerged cave passages of the state of Yucatan. The scope of this paper was to present an updated checklist and the first unified identifiaction guide for the morphological determination of these stygobiont crustaceans. We hope this study will motivate future researches to focus on the taxonomy of the highly endemic stygofauna of the groundwater ecosystems of the Yucatan Peninsula.

Acknowledgements

We are grateful to our colleagues of Cenoteando: namely Efraín Chavez-Solís, Luis Liévano-Beltrán, Quetzalli Hernández and Ricardo Merlos-Riestra for the realization of the field trips and their invaluable contribution in collecting the studied material. Sophia Drs, Silvia Reyes, Benjamín Magaña, Erick Sosa-Rodríguez and Kay Vilchis are also acknowledged for their assistance during the cave dives. We are grateful to Eduardo Velázquez and Alberto Guerra for the computer graphical editing of the line drawings and assembling the plates. Luis Manuel Mejía-Ortíz is highly acknowledged for the up to date information and literature provided about the anchialine decapods of the peninsula. We are grateful to Ahmad-Reza Katouzian, Daniel Previatteli and an anonymous reviewer for their useful suggestions, which helped us to improve the manuscript. Richard Wilson is acknowledged for the linguistic revision of the manuscript. DA is grateful for the grant provided by the "DGAPA-UNAM Programa de Becas Posdoctorales en la UNAM, 2019" and "DGAPA-UNAM Programa de Becas Posdoctorales en la UNAM, 2020". Financial support was provided by project PAPIIT IN222716 “Biodiversidad y Ecología de la fauna de cenotes de Yucatán” and “Hacía un mapa de biodiversidad acuática de cenotes de la península de Yucatán”, DGAPA-PAPIIT 2019 – IN228319 to NS.

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