UNED Research Journal (e-ISSN 1659-441X), Vol. 12(1): e2736, June, 2020

 

 

Crustaceans (Decapoda & Stomatopoda) from Golfo Dulce (Pacific, Costa Rica) in the collection of the Museum of Zoology, University of Costa Rica

 

Rita Vargas-Castillo1, 2 https://libapps-eu.s3.amazonaws.com/accounts/86186/images/iconoorcid_16x16.gif & José A. Vargas-Zamora1, 3 https://libapps-eu.s3.amazonaws.com/accounts/86186/images/iconoorcid_16x16.gif

1.        Universidad de Costa Rica, Escuela de Biología, 11501-2060, San José, Costa Rica

2.        Universidad de Costa Rica, Escuela de Biología, Museo de Zoología, 11501-2060, San José, Costa Rica; rita.vargas@ucr.ac.cr

3.        Universidad de Costa Rica, Centro de Investigación en Ciencias del Mar y Limnología (CIMAR), 11501-2060, San José, Costa Rica; jose.vargas@ucr.ac.cr

 

Recibido 14-I-2020 – Corregido 15-IV-2020 – Aceptado 28-IV-2020

DOI: https://doi.org/10.22458/ urj.v12i1.2736

 

 

ABSTRACT. Introduction: The availability of recently updated lists of species from a particular area is an important first step to evaluate changes in species composition and abundance. Golfo Dulce is a fjord-like embayment with relatively pristine shores and relatively deep waters (200m) that have been sampled occasionally for crustaceans. Methods: In this study the all species from Golfo Dulce deposited in the collection of the University of Costa Rica Museum of Zoology were listed and scientific names were updated. The MZUCR catalog number, station, substrate type, and year or collection were included for each species. Results: A total of 106 species were listed. Neogonodactylus zacae was present in four of the 19 stations represented in the collections for Golfo Dulce. Nine species were present in three stations, 19 in two stations and the remaining 77 in one station each. The families with most species were Ocypodidae y Palaemonidae (7) and Porcellanidae (14). Conclusions: Is necessary to improve our knowledge of the decapods and stomatopods fauna from Golfo Dulce through further samplings. Intertidal sites such as Golfito and Rincón bays have been poorly sampled as well as intertidal and subtidal environment from the western and eastern shores. However, the fauna is relatively rich when it is related to the area of Golfo Dulce (750km2) and is indicative of a relatively undisturbed environment. Updated management policies are urgently needed and this list of species is a step towards this goal.

 

 

 

 

 

 

 

 

 

 

Keywords: Biodiversity, eastern Tropical Pacific, Stomatopoda, Dendrobranchiata, Caridea, Anomura, Brachyura.

 

RESUMEN. “Crustáceos (Decapoda & Stomatopoda) del Golfo Dulce (Pacífico, Costa Rica) en la colección del Museo de Zoología, Universidad de Costa Rica”. Introducción: Las listas actualizadas de especies son un primer paso para evaluar cambios temporales en composición y abundancia. Golfo Dulce es un cuerpo de agua marino semejante a un fiordo, con costas poco alteradas y aguas relativamente profundas (200m). Métodos: Elaboramos una lista taxonómicamente actualizada de las especies de macro-crustáceos recolectados en Golfo Dulce y depositadas en la colección del Museo de Zoología de la Universidad de Costa Rica (MZUCR). El número de catálogo del MZUCR, estación, tipo de sustrato, y año de colecta fueron anotados para cada especie. Resultados: Hay 106 especies en la lista. Neogonodactylus zacae estuvo en cuatro de las 19 estaciones representadas en las colecciones para Golfo Dulce. Nueve especies en tres estaciones, 19 en dos estaciones y las restantes 77 en una estación cada una. Las familias con más especies fueron Ocypodidae y Palaemonidae (7) y Porcellanidae (14). Conclusiones: Se requieren más muestreos, particularmente en sitios entre mareas como las bahías de Golfito y Rincón; y fondos de entre mareas y submareales de las costas oeste y este. La fauna es relativamente rica considerando el área de Golfo Dulce (750 km2) y es indicadora de un ambiente relativamente inalterado. Se requiere urgentemente de políticas de manejo actualizadas y esta lista en un paso hacia ese objetivo.

 

 

 

 

 

 

 

 

 

Palabras clave: Biodiversidad, Pacifico Tropical Este, Stomatopoda, Dendrobranchiata, Caridea, Anomura, Brachyura.

 

 

Golfo Dulce is a deep embayment on the Pacific coast (08o30´N & 83o20’W) of Costa Rica. The water dynamics of the system were described by Svendsen, Rosland, Myking, Vargas, Lizano and Alfaro (2006). The gulf is characterized by an inner basin (200m) and a sill (70m) at the entrance (Fig. 1). The bathymetry of the gulf was described by Hebbeln, Beese and Cortés (1996). The presence of a deep basin, steep shores and a sill results in Golfo Dulce being considered essentially a tropical fjord-like embayment (Wolff, Hartmann, & Koch, 1996). Narrow shores with fringing mangrove forests, rocky outcrops, decaying coral reefs, and sandy beaches surround most of Golfo Dulce (Cortés, 1990; Samper-Villarreal & Silva-Benavides, 2015). Hypoxic and anoxic conditions are found in waters deeper than 100m (Córdoba & Vargas, 1996; Dalsgaard, Canfield, Peterson, Thamdrup, & Acuña-González, 2003), and no macrofaunal organisms have been found living in the anoxic basin sediments (León-Morales & Vargas, 1998).

                Information about the macro-crustacean fauna of Golfo Dulce is scarce. The most important survey was conducted by the R.V. Victor Hensen (1993-1994) which collected crustaceans over a depth range of 15 to 200m using Otter and beam trawls. A preliminary list of 50 macro-crustaceans from Golfo Dulce collected during the R.V. Victor Hensen survey was published by Vargas, Jesse and Castro (1996). In addition, Castro and Vargas (1996) listed 68 species of macro-crustaceans reported in the literature for Golfo Dulce and included additional data for those collected during the survey. The spatial distributions of the species collected by the research vessel were analysed by Jesse (1996). Voucher specimens from most of the survey were deposited in the collection of the Museum of Zoology, University of Costa Rica (MZUCR). Other specimens deposited in the MZUCR were obtained over the years during occasional visits to different sites around the estuary, but a planned inventory of the crustacean fauna of the estuary is yet to be conducted.

               Golfo Dulce is under the increasing pressure of local, regional and global stressors, such as pollution, coastal development, extraction of resources, and climate change (Morales-Ramírez, 2011, Morales-Ramírez, Acuña-González, Lizano, Alfaro, & Gómez, 2015). A trophic model in Golfo Dulce considering the key roles of the crustaceans and other groups was developed by Woff et al. (1996), but it needs to be updated. In this context, information on the biodiversity of Golfo Dulce is urgently needed as input in order to improve the trophic model and to develop of new management policies at the ecosystem level. Data on the previously recorded species from the gulf is important to evaluate changes in biodiversity over time and to identify sites of relevance for future surveys. Thus, the objective of this report is to provide an updated list of species of macro-crustaceans (Decapoda and Stomatopoda) from Golfo Dulce deposited in the collection of the UCR-Museum of Zoology, identify gaps of information, and make suggestions for a future survey of the fauna.

 

MATERIALS AND METHODS

 

The crustacean collection of the Museum of Zoology of the University of Costa Rica (MZUCR) is composed with three components. First, the collection of specimens preserved in 70% ethanol in labeled glass jars. Second, a dossier of handwritten catalog cards, with data for each collecting site. Third, a digital file filled with data obtained from the catalog cards. All catalog entries of marine macro-crustacean species belonging to Golfo Dulce were selected from the digital file. The handwritten cards and the specimen collection were reviewed when sampling data was not clear and/or the species identification was necessary to double-check records. A list of species was assembled, arranged in alphabetical order, and a code number assigned to each one. The list includes the presently accepted species name, authority, catalog number, station and year of collection. Other information such as depth (intertidal, subtidal) and substrate description (rocks, coral, sediment, other) was also included, when available. Two Golfo Dulce species are listed in the cards with no other station data. Most of the specimens in the collection were collected by hand and occasionally by SCUBA while those from the R.V. Victor Hensen expedition were captured with otter and beam trawl nets. All species names were verified for their currently accepted name based in the web page World Register of Marine Species (WORMS).

Ethical, conflict of interest and financial statements: The authors have fully complied with all pertinent and legal requirements both during the study and in the production of the manuscript. We state that there are no conflicts of interest of any kind. The financial sources are fully and clearly stated in the acknowledgements section and we fully.

 

RESULTS

 

In total, there were 19 stations for which information was available (Fig. 1). Intertidal and SCUBA diving stations were assigned a code number, while those from trawl nets were identified with capital letters. A total of 106 species of macrocrustaceans with 173 entries was available for Golfo Dulce and catalogued in the collection of the Museum of Zoology (Appendix 1). Of this total, 102 are decapods and four are stomatopods. The earliest collection records are from 1969, followed by a time gap, until 1990 and 1993-1995 when 83 (48%) new entries were listed, many as the result of the R.V. Victor Hensen survey. The next intensive sampling effort took place during 2012-2013. Thirty-nine of the collecting sites were coral rocks, while 32 stations were from sediments. Most of the collecting sites were intertidal. The maximum depth sampled was 200m (Appendix 1).

                The 102 species of decapods were distributed into 32 families, while the four species of stomatopods were represented by two (Table 1). The most specious family was the Porcellanidae, with 14 species. Other families, represented by five or more species, are: Ocypodidae (7), Palaemonidae (7), Alpheidae (6), Diogenidae (6), Xanthidae (6), Mithracidae (5), and Portunidae (5). Eleven families were represented by only one species (Table 1). There were ten most frequently species collected in the 19 stations (Table 2). Only one species, the stomatopod Neogonodactylus zacae, was collected at four stations. Nine species were found in three stations, 19 in two stations and the remaining 77 in only one station each. Station 12 had the most species (21), followed by stations 7 (17), 10 (16), 9 (15), and 3 (14). The other stations had less than 10 species each. Stations 1, 13, had one species each (Table 2). The R.V. Victor Hensen stations located near the sill and at the mouth of Golfo Dulce (F, H, and G, I) included 10, 5, 6, and 6 species, respectively. Those stations in deeper waters inside the gulf had 1 (L) and 3 (M) species.

 

Fig. 1. Location of the stations reported in this study in Golfo Dulce. 2-14, intertidal and shallow water; F, G, H, I, M, deep-water stations from the R.V. Victor Hensen survey (1993 / 1994). The gray shaded area encloses basin depths of 200 to 215m. Station F is located at the sill (70m).

 

TABLE 1

Families of crustaceans and number of species for each family catalogued in the collection of the Museum of Zoology. Golfo Dulce, Pacific coast of Costa Rica

 

DECAPODA

No. species

Alpheidae

6

Calappidae

1

Callianideidae

1

Cancridae

1

Chasmocarcinidae

1

Diogenidae

6

Dynomenidae

1

Gecarcinidae

1

Grapsidae

2

Hippidae

1

Hippolytidae

2

Leucosiidae

3

Mithracidae

5

Munididae

2

Ocypodidae

7

Oziidae

3

Paguridae

3

Palaemonidae

7

Pandalidae

2

Panopeidae

4

Penaeidae

3

Pilumnidae

2

Pinnotheridae

1

Porcellanidae

14

Portunidae

5

Processidae

1

Pseudorhombilidae

1

Sesarmidae

3

Sicyonidae

2

Solenoceridae

2

Upogebiidae

3

Xanthidae

6

STOMATOPODA

Gonodactylidae

1

Squillidae

3

 

 

TOTAL

106

 

 

TABLE 2

Species of crustaceans most frequently listed for the 19 stations, and stations where these were found; B. Total number of species reported at each station.

 

A. Species

Total

Station codes

Neogonodactylus zacae

4

6 - 8 - 10 - 12

Alpheus rostratus

3

6 - 8 - 12

Clibanarius lineatus

3

3 - 7 - 9

Goniopsis pulchra

3

3 - 7 - 9

Hemus finneganae

3

6 - 10 - 12

Munida gracilipes

3

1 - G - I

Palaemonella holmesi

3

6 - 8 - 10

Playpodiella rotundata

3

6 - 8 - 12

Pomatogebia rugosa

3

6 - 8 - 12

Processa peruviana

3

8 - 12 - I

 

 

 

B. Station

1 (1 sp), 2 (2), 3 (14), 4 (3), 6 (9), 7 (17), 8 (9), 9 (15), 10 (16), 11 (2), 12 (21), 13 (1),14 (2), F (10), G (6), H (5), I (6), L (1) M (3)

 

DISCUSSION

 

Because almost all the specimens of macrocrustaceans from Golfo Dulce were collected during occasional visits, there is yet to be an intensive sampling effort covering most of the diverse habitats around its shores and in deep waters. The specimens came from a wide variety of habitats. The northern shore is characterized by decaying coral reefs and steep walls while the southern shore has mostly sandy beaches and mangrove swamps. The eastern shore has sandy beaches and a more extense shallow sandy platform. The only survey of deep waters was performed by the R.V. Victor Hensen expedition and it was restricted to a few stations.

                Although sampling effort in Golfo Dulce has been relatively important, there is still much additional sampling needed to reach a reliable picture of the invertebrate biodiversity of the embayment. Of relevance are future collections in the area of Golfito Bay where only one entry is reported in the UCR Museum catalogue despite the relatively easy access to many of the environments around this shallow bay. Other relatively unexplored regions are intertidal and subtidal areas near Rincon Bay, the tip of the Osa peninsula, and the sandy beaches and shallow bottoms on the eastern shore. The fact that 77 species were found at only one station each supports the idea that each type of substrate appears to host a characteristic assemblage of species and emphasize the need to explore other sites characterized by different types of substrates.

                According to Morales-Ramírez (2011), Golfo Dulce contains 21,5% of the marine biodiversity of the Pacific coast of Costa Rica in an area of about 750km2. He also reported a total of 1022 species of different animal groups (invertebrates and vertebrates) for Golfo Dulce. This total represents nearly 1,36 species per km2, a figure considered by Morales-Ramírez (2011) to be nearly double than that of the larger (1 990km2) and shallower Gulf of Nicoya estuary, where a more intensive sampling effort has been conducted (Vargas, 2016; Vargas-Zamora, Vargas-Castillo, & Sibaja-Cordero, 2019)

                Despite of some local pollution problems (Spongberg & Davis, 1998; Spongberg, 2004; García, Acuña-González, Vargas-Zamora, & García-Céspedes, 2006; Spongberg et al., 2011), the biodiversity of Golfo Dulce appears to indicate a relatively healthy ecosystem (Morales-Ramírez et al., 2015). In this context updated information on the biodiversity of the estuary may contribute to a better management of its resources and attract interested visitors. In addition, updated lists are a first step to evaluate structural community changes due to local, regional or global stressors such as coastal development, pollution, and climate change. This list of selected groups of macrocrustaceans presented herein is a step towards these goals.

 

ACKNOWLEDGMENTS

 

We thank two anonymous reviewers for comments on an earlier draft, and Sergio Aguilar for preparing Fig. 1. This is a contribution of Zoology Museum, Biology School, University of Costa Rica

 

REFERENCIAS

 

Castro, M., & Vargas, R. (1996) Annotated list of species of marine crustaceans (Decapoda and Stomatopoda) from Golfo Dulce, Costa Rica. Revista de Biología Tropical, 44 (Supplement 3), S87 - S95.

 

Cortés, J. (1990). The coral reefs of Golfo Dulce, Costa Rica: distribution and community structure. Atoll Research Bulletin, 344, 1 - 37. DOI: 10.5479/si.00775630.344.1

 

Córdoba, R., & Vargas, J. A. (1996). Nutrient profiles at a 200 m deep station in Golfo Dulce, Costa Rica. Revista de Biología Tropical, 44 (Supplement 3), S233 - S236.

 

Dalsgaard, T., Canfield, D. E., Peterson, J., Thamdrup, B., & Acuña-González, J. (2003). N2 production by the anammox reaction in the anoxic water column of Golfo Dulce, Costa Rica. Nature, 422, 606 - 608. DOI: 10.1038/nature01526

 

García, V., Acuña González, J., Vargas Zamora, J. A., & García Céspedes, J. (2006). Calidad bacteriológica y desechos sólidos en cinco ambientes costeros de Costa Rica. Revista de Biología Tropical, 54 (Supplement 1), S35 - S48.

 

Hebbeln, D., Beese, D., & Cortés, J. (1996). Morphology and sediment structures in Golfo Dulce, Costa Rica. Revista de Biología Tropical, 44 (Supplement 3), S1 - S10

 

Jesse, S. (1996). Demersal crustacean assemblages along the Pacific coast of Costa Rica: a quantitative and multivariate assessment based on the Victor Hensen Costa Rica Expedition (1993 / 1994). Revista de Biología Tropical, 44 (Supplement 3), S115 - S134.

 

León-Morales, R., & Vargas, J. A. (1998). Macroinfauna of a tropical fjord-like embayment, Golfo Dulce, Costa Rica.  Revista de Biología Tropical, 46 (Supplement 6), S81 - S90.

 

Morales-Ramírez, A. (2011). La diversidad marina del Golfo Dulce, Pacífico sur de Costa Rica: amenazas a su conservación. Biocenosis, 24, 9 - 20.

 

Morales-Ramírez, Á., Acuña-González, J., Lizano, O., Alfaro, E., & Gómez, E. (2015). Rasgos oceanográficos en el Golfo Dulce, Pacífico de Costa Rica: una revisión para la toma de decisiones en conservación marina. Revista de Biología Tropical, 63 (Supplement 1), S131 - S160.

 

Samper-Villarreal, J., & Silva-Benavides, A. M. (2015). Complejidad estructural de los manglares de Playa Blanca, Escondido y Rincón de Osa, Golfo Dulce, Costa Rica. Revista de Biología Tropical, 63 (Supplement 1), S199 - S208.

 

Svendsen, H., Rosland, R., Myking, S., Vargas, J. A., Lizano, O. G., & Alfaro, E. J. (2006). A physical-oceanographic study of Golfo Dulce, Costa Rica. Revista de Biología Tropical, 54 (Supplement 1), S147 - S170.

 

Spongberg, A. I., & Davis, P. (1998). Organochlorinated pesticide contaminants in Golfo Dulce, Costa Rica. Revista de Biología Tropical, 46 (Supplement 6), S111 - S124.

 

Spongberg, A. I. (2004). PCB contamination in marine sediments from Golfo Dulce, Pacific Costa Rica. Revista de Biología Tropical, 52 (Supplement 2), S23 - S32.

 

Spongberg, A. L., Witter, J. D., Acuña, J., Vargas, J. A., Murillo, M., Umaña, G., Gómez, E., & Pérez, G. (2011). Reconnaissance of selected Pharmaceutical and Personal Care Product compounds in Costa Rican surface waters. Water Research, 45, 6709 - 6717. DOI: 10.1016/j.watres.2011.10.004

 

Vargas, R., Jesse, S., & Castro, M. (1996). Checklist of crustaceans (Decapoda and Stomatopoda), collected during the Victor Hensen Costa Rica Expedition (1993 / 1994). Revista de Biología Tropical, 44 (Supplement 3), S97 - S102.

 

Vargas, J. A. (2016). The Gulf of Nicoya estuarine ecosystem. In. M. Kaapelle (Ed.). Ecosystems of Costa Rica Chicago (pp. 106-124). Chicago, USA: University of Chicago Press.

 

Vargas-Zamora J. A., Vargas-Castillo, R., & Sibaja Cordero, J. A. (2019). Crustáceos (Decapoda y Stomatopoda) del R.V. Skimmer y R.V. Victor Hensen en el Golfo de Nicoya, Pacifico. Costa Rica. Revista de Biología Tropical, 67, 286 - 305. DOI: 10.15517/rbt.v67i1.34729

 

Wolff, M., Hartmann, H. J., & Koch, V. (1996). A pilot trophic model for Golfo Dulce: a fjord-like embayment, Costa Rica. Revista de Biología Tropical, 44 (Supplement 3), S215 - S231.


 

APPENDIX 1

List of species of Decapoda and Stomatopoda collected in Golfo Dulce and deposited in the collection of the Museum of Zoology (MZUCR), University of Costa Rica: E = endosymbiont in a clam, I = intertidal, CR = coral rock, GD = Golfo Dulce, S = sediment, SC = soft coral, M = mangrove, PT = polychaete tubes, R = rocks, WR = worm reef. No data =?  

 

Species

Catalog code, station, depth, substrate, year of collection

DECAPODA

01.

Acantholobulus mirafloresensis Abele & Kim, 1989

1455-01 / 3 / 0 m / ? / 1990

02.

Achelous asper (A. Milne-Edwards, 1861)

2104-06 / F / 70 m / S / 1994

 

 

207-01 / 14 / 18 m / S / 1969

03.

Achelous iridescens (Rathbun, 1894)

2005-06 / I / 160-200 m / S /1993

04.

Ala cornuta (Stimpson, 1860)

3162-17 / 12 / 1-2 m / CR / 2013

 

 

3483-01 / 12 / ? / CR / 2013

05.

Alpheus bellimanus Lockington, 1877

3204-01 / 10 / 27 m / CR / 2012

06.

Alpheus floridanus Kingsley, 1878

2006-02 / G / 200 m / S /1994

07.

Alpheus hebes W. Kim & Abele, 1988

2929-02 / 10 / 0 m / I / 2012

08.

Alpheus pacificus Dana, 1852

2929-03 / 10 / 0 m / I / 2012

09.

Alpheus panamensis Kingsley, 1878

3162-03 / 12 / 1-2 m / CR / 2013

10.

Alpheus rostratus W. Kim & Abele, 1988

3405-06 / 6 / 8-10 m / CR / 2013

 

 

3185-08 / 8 / 1-2 m / CR / 2013

 

 

3162-04 / 12 / 1-2 m / CR / 2013

11.

Aratus pacificus Thiercelin & Schubart, 2014

499-01 / 7 / 0 m / M / 1969

12.

Calcinus obscurus Stimpson, 1859

1370-06 / 3 / 0 m / I, R, M /1990

 

 

1368-06 / 9 / 0 m / M / 1990

13.

Callianidea mariamartae Hernaez & Vargas, 2013

2928-01-02 / 10 / 0 m / I, R / 2012

 

 

2929-01 / 10 / 0 m / I, R / 2012

 

 

2957-01 / 10 / 0 m / I, R / 2012

14.

Callinectes arcuatus Ordway, 1863

2104-05 / F / 70 m / S / 1994

 

 

502-01 / 7 / ? / ? / 1969

15.

Cancer johngarthi Carvacho, 1984

2005-00 / I /160-200 m / S /1993

16.

Cardisoma crassum Smith, 1870

434-01 / 7 / 0 m / ? / 1969

 

 

515-01 / 7 / 0 m / ? / 1969

 

 

1365-02 / 7 / 0 m / M / 1990

17.

Chasmocarcinus latipes Rathbun, 1898

1995-04 / F / 70 m / S /1993

 

 

2006-03 / G / 200 m / 1994

18.

Clibanarius albidigitus Nobili, 1901

1370-05 / 3 / 0 m / I, R, M /1990

19.

Clibanarius lineatus (H. Milne Edwards, 1848)

870-01 / 7 / 0 m / ? / 1969

 

 

1370-04 / 3 / 0 m / I, R, M /1990

 

 

1368-07 / 9 / 0 m / M / 1990

20.

Cronius ruber Lamarck, 1818

2846-02 / 6 / ? / ? / 2011

21.

Cyrtoplax schmitti Rathbun, 1935

1446-01 / 9 / 0 m / ? / 1990

 

 

1447-01 / 9 / 0 m / ? / 1990

 

 

1454-01 / 11 / 0 m / M / 1990

 

 

1456-02 / 11 / 0 m / ? / 1990

22.

Dardanus nudus Ayón-Parente & Hendrickx, 2009

1995-05 / F / 70 m / S /1993

23.

Dardanus sinistripes (Stimpson, 1858)

2007-03 / H / 15-20 m / S / 1993

24.

Emerita rathbunae Schmitt, 1935

2794-01 / GD / 0 m / ? / 1995

25.

Epixanthus tenuidactylus (Lockington, 1877)

1370-02 / 3 / 0 m / I, R, M /1990

26.

Eurypanopeus canalensis Abele & Kim, 1989

1453-02 / 9 / 0 m / ? / 1990

 

 

1466-04 / 9 / 0 m / ? / 1990

27.

Eurypanopeus transversus (Stimpson, 1860)

448-01 / 7 / 0 m / M / 1969

 

 

1452-02 / 3 / 0 m / ? / 1990

28.

Eurytium tristani Rathbun, 1906

501-01 / 7 / 0 m / ? /1969

 

 

1369-02 / 7 / 0 m / M / 1990

29.

Gnathophyllum panamense (Faxon, 1893)

3162-06 / 12 / 1-2 m / CR / 2013

30.

Goniopsis pulchra Lockington, 1877

498-01 / 7 / 0 m / M / 1969

 

 

1362-05 / 7 / 0 m / M / 1990

 

 

1366-02 / 9 / 0 m / M / 1990

 

 

1368-04 / 9 / 0 m / M / 1990

 

 

1452-01 / 3 / 0 m / ? / 1990

31.

Hemus finneganae Garth, 1958

3077-03 / 10 / 27 m / R / 2012

 

 

3162-18 / 12 / 1-2 m / CR / 2013

 

 

3405-08 / 6 / 8-10 m / CR / 2013

32.

Hepatus kossmanni Neumann, 1878

266-01 / 14 / 18 m / S / 1969

33.

Heterocarpus vicarius Faxon, 1893

2005-02 / I / 160-200 m / S /1993

34.

Hirsutodynomene ursula (Stimpson, 1860)

1995-02 / F / 70 m / S / 1993

35,

Leptuca oerstedi (Ratbun, 1904)

1362-04 / 7 / 0 m /1990

36.

Leptuca terpsichores (Crane, 1941)

1463-01 / 3 / 0 m / S / 1990

37.

Leucosilia jurinii (de Saussure, 1853)

500-01 / 7 / 0 m / M /1969

38.

Lysmata californica (Stimpson, 1856)

2007-02 / H / 15-20 m / S /1993

39.

Megalobrachium erosum (Glassell, 1936)

3162-14 / 12 / 1-2 m / CR / 2013

40.

Megalobrachium pacificum (Gore & Abele, 1974)

1966-01 / 3 / ? / ? / 1990

 

 

2402-01 /10 / ? / WR / 1997

41.

Microcassiope xantusii Stimpson, 1871

3405-09 / 6 / 8-10 m / CR / 2013

42.

Munida gracilipes Faxon, 1893

2005-03 / I / 160-200 m / S /1993

 

 

2006-01 / G / 200 m / S / 1994

 

 

3578-01 / 01 / ? / S / 2004

43.

Ocypode gaudichaudii H. Milne Edwards & Lucas,1843

1370-03 / 3 / 0 m / I, R, M /1990

44.

Orthochela pumila Glassell, 1936

3312-01 / 2 / 11,3 m / SC / 2013

45.

Ozius perlatus Stimpson, 1860

2402-03 /10 / ? / WR / 1997

46.

Ozius verreauxii Saussure, 1853

1368-05 / 9 / 0 m / M / 1990

 

 

2131-01 / 9 / 0 m / ? / 1990

 

 

1367-01 / 10 / 0 m / R / 1990

47.

Pachygrapsus transversus (Gibbes, 1850)

1368-02 / 9 / 0 m / M / 1990

 

 

1362-06 / 7 / 0 m / M /1990

48.

Paguristes holmesi Glassell, 1937

1970-01 / G / 200 m / S /1994

49.

Pagurus virgulatus (Haig & Harvey, 1991)

3185-11 / 8 / 1-2 m / CR / 2013

50.

Palaemon gracilis (Smith, 1871)

1145-01 / 11 / 0.5 m / S / 1979

51.

Palaemonella holmesi (Nobili, 1907)

3077-06 / 10 / 27 m / R / 2012

 

 

2846-01 / 6 / ? / ? / 2011

 

 

3405-07 / 6 / 8-10 m / CR / 2013

 

 

3185-02 / 8 / 1-2 m / CR / 2013

52.

Panopeus purpureus Lockington, 1877

503-01 / 7 / 0 m / ? / 1969

 

 

1368-03 / 9 / 0 m / M / 1990

 

 

1369-01 / 7 / 0 m / M / 1990

53.

Pantomus affinis Chace, 1937

2005-01 / I / 200 m / S /1993

 

 

2009-01 / I / 160-200 m / S /1993

54.

Penaeus brevirostris Kingsley, 1878

2008-01 / M / 80-110 m / S /1993

55.

Penaeus californiensis Holmes, 1900

2008-01 / M / 110 m / S /1993 

56.

Periclimenaeus spinosus Holthuis, 1951

3405-05 / 6 / 8-10 m / CR / 2013

57.

Periclimenes infraspinis (Rathbun, 1902)

2243-1-2-3 / 10 / 9.5 m / SC / 1997

 

 

3187-03 / 10 / ? / SC /1997

58.

Persephona subovata (Rathbun, 1894)

262-01 / GD / 90 m / ? /1969

59.

Petramithrax pygmaeus Bell, 1835

3162-01 / 12 / 1-2 m / CR / 2013

 

 

3478-01 /12 / ? / CR / 2013

60.

Petrolisthes agassizii Faxon, 1895

3162-13 / 12 / 1-2 m / CR / 2013

61.

Petrolisthes armatus (Gibbes, 1850)

1465-01 / 9 / 0 m / ? / 1990

 

 

1466-05 / 9 / 0 m / ? / 1990

 

 

1817-01 / 3 / 0 m / S / 1990

 

 

2194-02 / 3 / 0 m / ? / 1997

62.

Petrolisthes glasselli Haig, 1957

3162-16 / 12 / 1-2 m / CR / 2013

63.

Petrolisthes robsonae Glassell, 1945

2194-03 / 3 / 0 m / ? / 1997

64.

Petrolisthes tonsorius Haig, 1960

1466-01 / 9 / 0 m / ? / 1990

65.

Petrolisthes tridentatus Stimpson, 1859

1466-02 / 9 / 0 m / ? / 1990

66.

Petrolisthes zacae Haig, 1968

2227-01 / 7 / 0 m / M / 1990

 

 

2232-01 / 7 / 0 m / M / 1990

67.

Pilumnus limosus Smith, 1869

3162-21 / 12 / 1-2 m / CR / 2013

 

 

3185-05 / 8 / 1-2 m / CR / 2013

68.

Pilumnus townsendi Rathbun, 1923

3077-02 / 10 / 27 m / R / 2012

 

 

3108-01 / 4 / 12-22 m / CR / 2012

69.

Pinnixa longipes (Lockington, 1876)

3413-01 / 10 / 10 m / PT / 2014

70.

Pisidia magdalenensis (Glassell, 1936)

3162-15 / 12 / 1-2 m / CR / 2013

71.

Pitho quinquedentata Bell, 1835

3162-11 / 12 / 1-2 m / CR / 2013

72.

Platyactaea dovii (Stimpson, 1871)

3162-08 / 12 / 1-2 m / CR / 2013

73.

Platypodiella rotundata (Stimpson, 1860)

3405-03 / 6 / 8-10 m / CR / 2013

 

 

3162-09 / 12 / 1-2 m / CR / 2013

 

 

3185-06 / 8 / 1-2 m / CR / 2013

74.

Pleuroncodes monodon (A. Milne Edwards, 1837)

2005-07 / I / 160-200 m / S /1993

75.

Polyonyx nitidus Lockington, 1878

3108-05  / 4 / 12-22 m / CR / 2012

76.

Polyonyx quadriungulatus Chace, 1956

3413-02 / 10 / 10 m / PT/ 2014

77.

Pomatogebia rugosa (Lockington, 1878)

2200-01 / 6 / ? / ? / 1996

 

 

3162-23 / 12 / 1-2 m / CR / 2013

 

 

3405-04 / 6 / 8-10 m / CR / 2013

 

 

3185-03 / 8 / 1-2 m / CR / 2013

78.

Pontonia margarita Verrill, 1869

3186-01 / 8 / 1-2/ E / 2013

 

 

3188-01 / 8 / 1-2 / E / 2013

79.

Portunus xantusii (Faxon, 1893)

2104-02 / F / 70 m / S /1994

80.

Processa peruviana Wicksten, 1983

2005-06 / I / 160-200 m / 1993

 

 

3162-05 / 12 / 1-2 m / CR / 2013

 

 

3185-04 / 8 / 1-2 m / CR / 2013

81.

Pseudoveleronia laevifrons (Holthuis, 1951)

3434-03 / 2 / 11. m / SC / 2013

82.

Rimapenaeus pacificus Burkenroad, 1934

2008-02 / M / 80-110 m / 1993

83.

Sesarma rhizophorae Rathbun, 1906

1368-01 / 9 / 0 m / M / 1990

 

 

1366-03 / 7 / 0 m / M / 1990

 

 

1365-06 / 7 / 0 m / M / 1990

84.

Sesarma rubinofforum Abele, 1973

1365-08 / 7 / 0 m / M / 1990

85.

Sesarma sulcatum Smith, 1870

1365-01 / 7 / 0 m / M / 1990

86.

Sicyonia disedwardsi (Burkenroad, 1934)

1995-01 / F / 70 m / S /1993

87.

Sicyonia picta Faxon, 1893

2005-04 / I / 160-200 m / S /1993

88.

Solenocera agassizii (Faxon, 1893)

2006-04 / G / 200 m / S /1994

 

 

2007-01 / H / 15-20 m / S /1994

89.

Solenocera mutator Burkenroad, 1934

2105-01 / L /  200 m / S /1993

90.

Teleophrys cristulipes  Stimpson, 1860

3162-22 / 12 / 1-2 m / CR / 2013

 

 

3478-02 /12 / ? / CR / 2013

91.

Tomopagurus merimaculosus (Glassell, 1937)

2104-03 / F /70 m / S /1994

92.

Tomopagurus purpuratus (Benedict, 1892)

1995-03 / F / 70 m / S / 1993

 

 

2104-04 / F / 70 m / S / 994

93.

Trachycaris restricta (A. Milne-Edwards, 1878)

3108-03 / 4 / 12-22 m / CR / 2012

94.

Uca heteropleura (Smith, 1870)

1445-01 / 9 / 0 m / ? / 1990

95.

Uca princeps (Smith, 1870)

1362-03 / 7 / 0 m / S / 1990

96.

Uca stylifera (H. Milne Edwards, 1852)

1364-01 / 9 / 0 m / M / 1990

97.

Ucides occidentalis (Ortmann, 1897)

413-01 / 7 / 0 m / ? / 1969

 

 

1399-01 / 7 / 0 m / M / 1990

98.

Uhlias ellipticus Stimpson, 1871

3162-10 / 12 / 1-2 m / CR / 2013

 

 

3077-07 / 10 / 27 m / R / 2012

99.

Upogebia longipollex (Street, 1851)

3112-01 / 10 / 0 m / I / 2012

 

 

2402-02 / 10 / ? / WR / 1997

 

 

3210-01 / 10 / 0 m / I / 2012

100.

Upogebia spinigera (Smith, 1871)

1727-01 / 9 / 0 m / ? / 1990

 

 

2194-01 / 3 / 0 m / ? / 1997

101.

Williamstimpsonia stimpsoni (A. Milne-Edwards, 1879)

 3162-19 / 12 / 1-2 m /CR / 2013

102.

Xanthodius sternberghii (Stimpson,1859)

1370-01 / 3 / 0 m / I, R, M /1990

STOMATOPODA

103.

Neogonodactylus zacae (Manning, 1972)

3077-10 / 10 / 27 m / R / 2012

 

 

3162-12 / 12 / 1-2 m / CR / 2013

 

 

3185-07 / 8 / 1-2 m / CR / 2013

 

 

3405-11 / 6 / 8-10 m / CR / 2013

104.

Squilla biformis Biguelow, 1891

2006-05 / G / 200 m / S / 1994

105.

Squilla hancocki  Schmitt, 1940

195-02 / GD / 101 m / ? / 1969

106.

Squilla panamensis Bigelow, 1891

2104-01 / F / 70 m / S / 1994