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To validate the utility and performance of the gastro-laryngeal tube (GLT) in terms of cardiologist and patient satisfaction levels, incidence of and attempts at successful transesophageal echocardiography (TEE) probe placement, perioperative and postoperative hemodynamics, and adverse events related to the TEE procedure.In this randomized prospective clinical study, forty-four patients undergoing TEE and aged 20 to 80 years old scheduled for TEE were randomly allocated to two study groups: Group SA (sedation and analgesia) and Group GLT. Cardiologist and patient satisfaction levels, TEE probe placement performance, hemodynamics, adverse events related to the TEE procedure, demographic characteristics, and TEE procedure data were recorded.The cardiologist satisfaction level was significantly higher in Group GLT (P = .011). The TEE probe was successfully placed at the first attempt in all the patients in Group GLT and at the first attempt in 11 patients, at the second attempt in 8 patients, and at the third attempt in 3 patients in Group SA. The TEE probe placement success was significantly higher in Group GLT (P .001), and TEE probe placement was significantly easier in Group GLT (P .001). There were no significant differences in patient satisfaction, heart rate, mean arterial pressure, oxygen saturation, adverse events related to the TEE procedure between the groups.The present study revealed that GLT use elicited a higher cardiologist satisfaction level and resulted in more successful and easier TEE probe placement. We thus conclude that the use of the recently developed GLT may ensure airway management safety and a comfortable TEE experience.

Objective: This study aims to investigate the mortality factors in hemodialysis patients and kidney transplant patients with COVID-19 patients. Method: The demographic, clinic, laboratory, and radiologic signs of the kidney transplant and hemodialysis patients diagnosed with COVID-19 between 11 March 2020-11 March 2021 were evaluated. Results: To this study, 72 hemodialysis (median age, 57.5 Q1-Q3:43-65; female:36/50%) and 58 kidney transplant (median age, 44.5 Q1-Q3:28.75-55.25; female:21/36.2%) were included. Fifteen HD patients (20.8%) died. To identify the independent predictors of in-hospital mortality, multivariable logistic regression analyses were performed using the variables in the univariate analyses including age, female gender, diabetes mellitus, ferritin, d-dimer, albumin, CRP, procalcitonin, dyspnea. Age (OR:1.12, 95% [CI]: 1.03-1.21, p=0.004), and dyspnea (OR: 9,7 95% CI 1.80-52.2, p=0.008) were found to be associated with in-hospital mortality. Nine (15.5%) of transplant patients died. The median time from the beginning of symptoms to the time of admission was 3 days (2-5). And this rate was 2 (2-3) and 5 (4-5.75) days, respectively, for patients followed up in our center and the external centers (p

Einführung: Spezifische Implantat Magnet Modifikation oder Schraubenfixierungen erlauben in Kombination mit einer distalen Positionierung des Cochlear Implantates eine schmerzfreie Beurteilung von innerem Gehörgang, Cochlea sowie intracochleärer Elektrodenlage mittels MRT nach der CI [zum vollständigen Text gelangen Sie über die oben angegebene URL], 22. Jahrestagung der Deutschen Gesellschaft für Audiologie

52nd Conference of the European-Society-of-Human-Genetics (ESHG) -- JUN 15-18, 2019 -- Gothenburg, SWEDEN, Avci, Cigir Biray/0000-0001-8251-4520, WOS: 000489313904120, [No abstract available], European Soc Human Genet

52nd Conference of the European-Society-of-Human-Genetics (ESHG) -- JUN 15-18, 2019 -- Gothenburg, SWEDEN, Avci, Cigir Biray/0000-0001-8251-4520, WOS: 000489313904119, [No abstract available], European Soc Human Genet

51st Conference of the European-Society-of-Human-Genetics (ESHG) in conjunction with the European Meeting on Psychosocial Aspects of Genetics (EMPAG) -- JUN 16-19, 2018 -- Milan, ITALY, Avci, Cigir Biray/0000-0001-8251-4520, WOS: 000489313107340, [No abstract available], European Soc Human Genet

52nd Conference of the European-Society-of-Human-Genetics (ESHG) -- JUN 15-18, 2019 -- Gothenburg, SWEDEN, Avci, Cigir Biray/0000-0001-8251-4520, WOS: 000489313904061, [No abstract available], European Soc Human Genet

52nd Conference of the European-Society-of-Human-Genetics (ESHG) -- JUN 15-18, 2019 -- Gothenburg, SWEDEN, Avci, Cigir Biray/0000-0001-8251-4520, WOS: 000489313904180, [No abstract available], European Soc Human Genet

52nd Conference of the European-Society-of-Human-Genetics (ESHG) -- JUN 15-18, 2019 -- Gothenburg, SWEDEN, Avci, Cigir Biray/0000-0001-8251-4520, WOS: 000489313904153, [No abstract available], European Soc Human Genet, Ege University Scientific Research Projects CoordinationEge University, Our study is supported by Ege University Scientific Research Projects Coordination.

51st Conference of the European-Society-of-Human-Genetics (ESHG) in conjunction with the European Meeting on Psychosocial Aspects of Genetics (EMPAG) -- JUN 16-19, 2018 -- Milan, ITALY, Avci, Cigir Biray/0000-0001-8251-4520, WOS: 000489313104047, [No abstract available], European Soc Human Genet

Enallopaguropsis guatemoci (Glassell, 1937) (Figs. 1 A���E, 2A���G) Material examined. The ovigerous female used in this study (LC = 2.1 mm) had 17 eggs, but only eight zoeae hatched (four zoea measured and/or dissected), 19 April 2011 (ICML-EMU 10879). Size of zoeae, CL= 1.40 �� 0.03 mm (1.37���1.43 mm). Description. Carapace (Fig. 1 A, B). Moderately truncated, dorsolateral angles rounded, with dorsomedial keel extending to posterior margin; eyes sessile; pterygostomial region slightly produced; rostrum slightly deflected ventrally, long, moderately slender, slightly overreaching antennae. Antennule (Fig. 1 A, D). Subcylindrical, weakly segmented, shorter than antennae; 2 aesthetascs and 3 or 4 moderately long simple setae terminally; 1 long terminal plumose seta on endopodal bud. Antenna (Fig. 1 A, E). Exopod (scaphocerite) with moderately strong distal spine, inner margin convex with 8 long and 1 short plumose setae; endopod approximately three-fifths length of scaphocerite, with 2 long terminal plumose setae; protopod with strong serrate spine at base of endopodal junction. Mandibles (Fig. 2 A, B). Asymmetrically dentate; incisor processes with 1 strong tooth 1 or more smaller teeth; molar processes with several acute denticles and teeth; no palp bud. Maxillule (Fig. 2 C). Endopod 3-segmented, with 0 or 1, 1, 2 simple setae; coxal endite with 5 marginal plumose setae, 1 simple seta and 1 simple submarginal seta; basial endite with 2 strong teeth, each armed with several prominent accessory denticles, 1 simple marginal seta and 1 short, simple, submarginal seta. Maxilla (Fig. 2 D). Endopod bilobed, proximal lobe with 1 submarginal and 2 marginal plumodenticulate setae, distal lobe with 3 plumodenticulate marginal setae and outer margin with microtrichia; coxal and basal endites bilobed, proximal lobe of coxal endite with 1 submarginal and 6 marginal plumodenticulate setae and 1 lateral plumodenticulate seta, distal lobe with 1 submarginal and 2 or 3 marginal plumodenticulate setae; proximal lobe of basial endite with 1 submarginal and 3 marginal plumodenticulate setae, distal lobe with 1 submarginal and 3 marginal plumodenticulate setae; exopod (scaphognathite) fused to protopod, distal lobe with 5 marginal plumose setae, inner margin with microtrichia. First maxilliped (Fig. 2 E). No coxal seta; basis with 9 setae arranged 1, 2, 3, 3; endopod 5-segmented, setation (proximal to distal) 3, 2, 1, 2, 4 + I (I= an additional dorsolateral plumose seta); exopod 2-segmented, 4 long terminal, plumose natatory setae. Second maxilliped (Fig. 2 F). No coxal setae; basis with 1 marginal plumodenticulate seta in distal half, 2 plumodenticulate setae at inner, distal angle; endopod 4-segmented, segments 1���3 each with 2 plumodenticulate setae, distal segment with 4 + I plumose seta; exopod 2-segmented, 4 long terminal plumose, natatory setae. Third maxilliped (Fig. 2 G). Exopod unsegmented, smooth, with pointed or blunt tip. Abdomen (Fig. 1 A, B). Five somites and telson; first and second somites unarmed; posterodorsal margins of somites 3���5 each with pair of moderately long spines, posterolateral margins each with spines increasing in size distally. Telson (Fig. 1 A, C). Fused with 6th somite, moderately long, somewhat fan-shaped posteriorly; posterior margin with small V-shaped median notch, microtrichia and 7 + 7 setae (1, ii, 3���7), outermost (1st) unarmed, articulated, 2nd anomuran hair (ii), 3rd through 7th articulated, with plumose setae, 4th the longest, 0.70 times the width of telson measured at posterior margin; anal spine absent., Published as part of Ay��n-Parente, Manuel & Hendrickx, Michel E., 2017, First zoeal stage of the hermit crab Enallopaguropsis guatemoci (Glassell, 1937) (Crustacea: Anomura: Paguroidea: Paguridea) obtained in the laboratory, pp. 359-368 in Zootaxa 4227 (3) on pages 360-361, DOI: 10.11646/zootaxa.4227.3.4, http://zenodo.org/record/268338

PubMedID: 28748902 Drug reaction with eosinophilia and systemic symptoms (DRESS) or drug-induced hypersensitivity is a severe adverse drug-induced reaction. Aromatic anticonvulsants, such as phenytoin, phenobarbital, and carbamazepine, and some drugs, can induce DRESS. Atypical crystalluria can be seen in patients treated with amoxycillin or some drugs and can cause acute renal failure. We describe a 66-year-old man who presented fever and rash and acute renal failure three days after starting amoxycillin. He was also using phenytoin because of cerebral metastatic lung cancer. Investigation revealed eosinophilia and atypical crystalluria. The diagnosis of DRESS syndrome was made, amoxicillin was stopped, and dose of phenytoin was reduced. No systemic corticosteroid therapy was prescribed. Symptoms began to resolve within three to four days. The aim of this paper is to highlight the importance of microscopic examination of urine in a case with acute renal failure and skin lesions to suspect DRESS syndrome.

Areopaguristes praedator (Glassell, 1937) nov. comb. (Figs. 1���3) Paguristes praedator Glassell, 1937: 243, 245.��� Haig et al., 1970: 18, 27.��� Moran & Dittel, 1993: 601.��� Garc��a-Madrigal, 1999: 924.��� Hendrickx & Harvey, 1999: 370.��� Boschi, 2000: 104.��� Vargas & Cort��s, 2006: 480.���McLaughlin et al., 2010: 23. Paguristes preadator.���Rodr��guez de la Cruz, 1987: 86 (misspelling). Stratiotes praedator.���Ay��n-Parente, 2009: 232, Figs. 117���119.��� Ay��n-Parente & Hendrickx, 2010 a: 4. Type material. Holotype: male (SL 3.5 mm), 5.4 km NW from Cabo Pulmo, Baja California, Gulf of California, Mexico, 23 �� 28 'N, 109 �� 24 'W, 1 May 1936, Zaca sta 136 D- 27, sandy bottom with rocks, 91 m, coll. W. Beebe, AMNH- 12232 ex. 36782. Paratypes: 1 male (SL 1.2 mm), Bah��a Santa In��s, Baja California, Mexico, 26 �� 59 ��� 38 ''N, 111 �� 59 ���W, 10 Apr 1936, Zaca sta 141 D-4, 6 m, coll. W. Beebe, AMNH- 12521; 1 male (SL 3.4 mm), Banco Gordo, 23 �� 50 'N, 109 �� 28 'W, 21 Apr 1936, Zaca sta 150 D- 3, 104 m, coll. W. Beebe, AMNH- 12522; 11 males (SL 2.8���3.7 mm), Arena Bank, Baja California, Gulf of California, Mexico, 19 Apr 1936, Templeton Crocker Expedition, sta 136, coll. W. Beebe, 146 m, USNM 1076126. Type locality. 5.4 km NE of Cabo Pulmo, Baja California, Gulf of California, Mexico. Additional material. EMU holdings: 11 males, 13 females, 1 juv, 3 NS, off Teacap��n, Sinaloa, Mexico, 22 �� 17 ' 36 ''N, 106 �� 10 ' 54 ''W, 23 Apr 1981, SIPCO I, sta A 2, ot, 61 m, EMU- 6970; 41 males (SL 1.5���2.8 mm), 23 females (SL 0.9���2.6 mm), off Teacap��n, Sinaloa, Mexico, 22 �� 17 ' 36 ''N, 106 �� 10 ' 54 ''W, Apr 1981, SIPCO I, sta A 2, ot, 61 m, EMU- 10055; 2 males (NM), 1 female (NM), 2 NS, off Teacap��n, Sinaloa, Mexico, 22 �� 24 ' 18 ''N, 105 �� 54 ' 24 ''W, 23 Apr 1981, SIPCO I, sta A 1, oyster dredge, 35 m, EMU- 6964; 1 male (SL 2.8 mm), 1 female (SL 2.7 mm), off Mazatl��n, Sinaloa, Mexico, 23 ��08' 7 ''N, 106 �� 32 ' 8 ''W, 24 Aug 1981, SIPCO II, sta B 2, ot, 78 m, EMU- 6959; 2 males (SL 2.4 mm), off Teacap��n, Sinaloa, Mexico, 15 Jan 1982, SIPCO III, ot, EMU- 6963; 3 males (SL 1.6���2.9 mm), 1 female (SL 2.5 mm), off Punta Piaxla, Sinaloa, Mexico, 23 �� 37 ' 12 ''N, 106 �� 55 ' 54 ''W, 16 Jan 1982, SIPCO III, sta C 1, ot, 45 m, EMU- 6968 A; 2 males (SL 2.12���2.65 mm), same data, EMU- 6968 B; 11 males (SL 1.4���2.9 mm), 12 females (SL 1.7 ���2.0 mm), 17 NS (NM), Isla Carmen, 25 �� 58 'N, 111 ��07' 5 ''W, 4 May 1982, CORTES 1, sta 10, oyster dredge, 35���65 m, EMU- 10038; 1 ovig female (SL 2.9 mm), off Cabo San Miguel, Baja California, Mexico, 28 �� 7 ' 48 ''N, 112 �� 45 '06''W, 6 May 1982, CORTES 1, sta 20, ot, 68 m, EMU- 6965; 2 females (SL 3.1���3.7 mm), same data, EMU- 9598; 1 female (SL 2.5 mm), Rocas Consag, Gulf of California, 31 �� 8 ' 8 ''N, 114 �� 13 ' 1 "W, 16 Mar 1985, CORTES 1, sta 38, ot, 60 m, EMU- 6999; 1 NS (NM), off R��o Fuerte, Sinaloa, 25 �� 45 ' 30 ''N, 109 �� 34 ' 18 ''W, 12 May 1982, CORTES 1, sta 50, ot, 91 m, EMU- 6847; 2 males (SL 2.3���2.9 mm), off Banco Gordo, Baja California Sur, Mexico, 23 �� 5 ' 48 ''N, 109 �� 31 ' 54 ''W, 13 May 1982, CORTES 1, sta 57, ot, 56 m, EMU- 6997; 1 male (SL 2.5 mm), off Bah��a Santa Mar��a, Sinaloa, 24 �� 56 ' 42 ''N, 108 �� 44 ' 6 ''W, 10 Mar 1985, CORTES 2, sta. 4, ot, 64 m, EMU- 3701 A; 1 male (SL 3.2 mm), off Rocas Consag, Gulf of California, 31 �� 9 ' 18 ''N, 114 �� 15 ' 30 ''W, 16 Mar 1985, CORTES 2, sta. 38 bis, ot, 65 m, EMU- 3701 B; 1 NS (NM), off R��o Fuerte, Sinaloa, 25 �� 46 ' 12 ''N, 109 �� 35 '06''W, 20 Mar 1985, CORTES 2, sta 50, ot, 97 m, EMU- 6848; 11 males (SL 1.3���1.7 mm), 12 females (1.2 ���2.0 mm), 2 ovig females (SL 1.4 mm), 11 NS (NM), Rocas Consag, 31 ��09' N, 114 �� 15 ' 3 '' W, 0 9 May 1982, CORTES 1, sta 38, ot, 60 m, EMU- 10058; 3 males (SL 1.7���1.9 mm), 2 females (SL 1.8 ���2.0 mm), off Punta de Mita, Nayarit, Mexico, 20 �� 52 'N, 105 �� 32 ' 7 ''W, 14 May 1982, CORTES 1, sta 60, ot, 55���60 m, EMU- 10056; 1 male, Cabo San Miguel, Baja California, Gulf of California, 28 ��08' 30 ''N, 112 �� 42 ' 36 '' W, 6 May 1982, CORTES 1, sta 21, ot, 106 m, EMU- 6962; 3 males (SL 2.3���3.7 mm), off Bah��a Santa Mar��a, Sinaloa, Mexico 24 �� 56 ' 42 ''N, 108 �� 44 '06''W, 10 Mar 1985, CORTES 2, sta 4, ot, 64 m, EMU- 6966; 1 female (SL 2.8 mm), off Bah��a Santa Mar��a, Sinaloa, Mexico, 24 �� 56 ' 12 ''N, 108 �� 44 ' 30 ''W, 10 Mar 1985, CORTES 2, sta 5, ot, 110 m, EMU- 6957; 1 male (NM), off Rocas Consag, Gulf of California, Mexico, 31 �� 15 ' 12 ''N, 114 �� 22 '06''W, 16 Mar 1985, CORTES 2, sta 37, ot, 32 m, EMU- 6960; 18 males (NM), 17 females (NM), 1 NS, off Punta de Mita, Nayarit, Mexico, 20 �� 53 ' 54 '' N, 105 �� 27 ' 18 '' W, 23 Mar 1985, CORTES 2, sta 61, ot, 48 m, EMU- 6971; 4 NS (NW), off Punta Arboleda, 26 �� 46 ' 8 '' N, 110 ��06' 9 '' W, CORTES 2, sta 14, ot, 92 m, EMU- 4190; 1 male (SL 3.1 mm), same data, EMU- 10059; 3 NS (NM), Cabo San Miguel, Gulf of California, 28 �� 10 ' N, 112 �� 47 ' 7 '' W, 13 Mar 1985, CORTES 2, sta 19 -A, ot, 29 m, EMU- 4189; 1 female (SL 5.3 mm), same data, EMU- 10060; 1 female (SL 2.5 mm), 2 juv, 2 NS (NM), off Estero Tastiota, Sonora, Gulf of California, 28 �� 17 ' 8 '' N, 111 �� 37 ' 3 '' W, 18 Mar 1985, CORTES 2, sta 47, dredge, 34���37 m, EMU- 10061; 6 males (2.0��� 3.6 mm), 5 females (SL 2.0��� 3.3 mm), 2 NS, CORTES 2, sta 49 -A, ot, EMU- 10062; 18 males (SL 1.1���2.4 mm), 16 females (SL 1.2 ���2.0 mm), 7 NS (NM), off Punta Mita, Nayarit, Mexico, 20 �� 53 ' 54 ''N, 105 �� 27 ' 18 ''W, 23 Mar 1985, CORTES 2, sta 61, ot, 48 m, EMU- 10057; 1 NS (NM), off Punta de Mita, Nayarit, Mexico, 20 �� 51 ' 54 '' N, 105 �� 33 ' 12 ''W, 28 Jul 1985, CORTES 3, sta 60, ot, 70 m, EMU- 6958; 5 males (SL 4.1 ���5.0 mm), 2 females (SL 3.4���4.1 mm), 2 ovig females (SL 3.2���3.8 mm), 1 NS (NM), N of Isla Tibur��n, Gulf of California, 29 �� 11 ' 48 ''N, 112 �� 31 '06''W, 2 Aug 1985, CORTES 3, sta 25, ot, 80 m, EMU- 6967 A; 1 female (SL 3.1 mm), same data, EMU- 6967 B; 1 male (SL 2.5 mm), 1 NS (NM), off Estero Tastiota, Sonora, Mexico, 28 �� 19 ' 54 ''N, 111 �� 41 ' 16 ''W, 7 Aug 1985, CORTES 3, sta 47, Van Veen grab, 28 m, EMU- 6961; 1 female (SL 2.0 mm), NE of Isla ��ngel de la Guarda, Gulf of California, 29 �� 30 'N, 113 �� 24 'W, 17 Feb 1987, GUAYTEC I, ot, 105 m, EMU- 7448; 1 male (SL 3.9 mm), Gulf of California, Mexico, 26 �� 47 ' N, 110 ��06��W, GUAYTEC II, sta 4, ot, 85 m, EMU- 10064; 1 male (SL 3.6 mm), Gulf of California, Mexico, 27 ��00'N, 111 �� 50 'W, 2 Aug 1987, GUAYTEC II, sta 10, ot, 85���89 m, EMU- 10065; 7 males (SL 2.0��� 3.8 mm), 6 females (SL 1.7���3.1 mm), 8 ovig females (SL 1.5���2.7), Gulf of California, Mexico, 29 �� 29 'N, 113 �� 23 'W, 11 Aug 1987, GUAYTEC II, sta 69, 83��� 88 m, ot, EMU- 10066; 3 males (SL 1.9���2.8 mm), 1 female (SL 3.6 mm), off Piaxtla River, Sinaloa, Mexico, 23 �� 31 ' 54 ''N, 106 �� 52 ' 36 ''W, 14 Mar 1992, BIOCAPESS V, sta 6, ot, 62 m, EMU- 10063; 1 male (SL 3.1 mm), Cuenca Wagner-Consag, Gulf of California, Mexico, 30 �� 49 ' 57 ''N, 114 ��09' 48 ''W, 31 Jul 2010, sta 13 C, 162 m, EMU- 10067. CEC holdings: 10 males (SL 1.6 ���3.0 mm), 1 female (SL 1.9 mm), 4 juv, 10 NS (NM), Navidad, 1 Jun 1995, DEM I- 3, ot, 27 m; 2 males (SL 2.5���2. 7 mm), off Cuitzmala, Jalisco, Mexico, 19 �� 21.74 'N, 105 ��01.25'W, 13 Jun 1995, DEM I BIP V, sta 1, ot, 73 m; 1 male (SL 1.2 mm), 1 female (SL 1.2 mm), 1 ovig female (SL 1.5 mm), off Navidad Bay, Jalisco, Mexico, 19 �� 10.09 'N, 104 �� 42.06 'W, 20 Jun 1996, DEM IV- 3, ot, 73 m; 1 female (SL 2.2 mm), off Tenacatita, 25 May 1995, DEM I BIP V, sta 2, ot, 18 m; 1 male (SL 1.5 mm), off Manzanillo, Colima, Mexico, 19 ��03.06'N, 104 �� 22.09 'W, 6 Dec 1995, DEM II, ot, 73 m. LACM CR holdings: 1 male (SL 2.5 mm), Tenacatita Bay, Mexico, 18 Feb 1938, 45��� 72 m, MBPC 14304; 1 male (SL 1.8 m), ca 16 km SE off Puerto Pe��asco, Sonora, Gulf of California, Mexico, 2 Jul 1966, 14��� 18 m, MBPC 14306; 2 males (SL 3.5���3.8 mm), 5 females (SL 2.2���2.9 mm), Puerto Refugio, Angel de la Guarda Island, Gulf of California, Mexico, 21 Mar 1937, sta 708���39, 108 m, MBPC 14302; 7 males (SL 2.0��� 2.8 mm), Tenacatita Bay, Mexico, 18 Feb 1938, coll. S.A. Glassell, 45���72 m, MBPC 14306; 1 male (SL 2.8 mm), W of Puerto Libertad, Sonora, Gulf of California, Mexico, 30 Mar 1960, sta P- 211���60, 108 m, MBPC 14303; 14 males (SL 1.8���2.9 mm), 1 female (SL 2.1 mm), 28 juv (NM), off Teacapan, Sinaloa, Gulf of California, Mexico, sta P- 159 -60, 45��� 56 m, MBPC 14293; 1 male (SL 3.1 mm), SE of Isabel Island, Gulf of California, 8���9 Mar 1960, sta P- 157 ���60, 13��� 22 m, MBPC 14299; 1 male (SL 1.5 mm), off Punta Bah��a Kino, Sonora, 27 Mar 1960, sta P- 196 ���60, 23 m, MBPC 14292; 4 males (SL 2.5���2.8 mm), 1 female (SL 2.3 mm), NW of Isabel Island, Gulf of California, 10���11 Mar 1960, sta P- 158 ���60, 52��� 59 m, MBPC 14294; 1 male (SL 2.7 mm), off Punta Lesma, Sonora, Gulf of California, 22 Mar 1960, sta P- 170 -60, 59 m, MBPC 14297; 1 male (SL 2.8 mm), San Gabriel Bay, Espiritu Santo Island, Gulf of California, 20 Feb 1936, shoal, MBPC 14296; 1 male (SL 2.3 mm), E of Cabeza Ballena, Gulf of California, 3 Mar 1937, sta 620 ��� 37, MBPC 14295; 1 female (SL 1.8 mm), Agua Verde Bay, Gulf of California, 10 Mar 1937, sta 656 ���37, 45 m, MBPC 14298; 3 males (SL 2.2���2.8 mm), 4 females (SL 1.8���2.3 mm), 9 juv (NM), 4.5 km SW of SE point of Cleopha Island, Tres Mar��as Islands, Mexico, 8 Feb 1954, sta 2602 ���54, 36��� 74 m, MBPC 14300; 1 male (SL 3.3 mm), 2 females (2.8 ���3.0 mm), 1 juv (NM), N of ��ngel de la Guarda Island, Gulf of California, 5 Mar 1936, sta 546 ���36, 72��� 126 m, MBPC 14301. USNM holdings: 1 female (SL 1.6 mm), Gulf of California, 20 �� 28 'N, 113 ��06' 30 ''W, 24 Mar 1889, Albatross R/ V, sta 3019, 26 m, USNM 265362; 39 males (SL 1.7���2.8 mm), 27 females (SL 1.4���2.8 mm), 21 NS, in shell, Bah��a Banderas, Jalisco, Mexico, 20 �� 38 'N, 105 �� 23 'W, 13 Feb 1938, coll. S. A. Glassell, 46���73 m, USNM 1076129; 52 males (SL 1.4 ���3.0 mm), 22 females (SL 1.1���2.5 mm), 9 ovig females (SL 1.8���2.2 mm), Bah��a Chamela, Jalisco, Mexico, 16 Feb 1938, coll. S. A. Glassell, 46���55 m, USNM 1076337; 1 ovig female (SL 2.2 mm), 2 juv (SL 1.19 mm), Bah��a Chamela, Jalisco, Mexico, 16 Feb 1938, 46��� 55 m, id. S. A. Glassell, USNM 1107138; 5 males (SL 1.2���1.8 mm), 2 females (SL 1.0��� 1.3 mm), 1 juv (SL 0.9 mm), Secas Island, SW group, Gulf of Chiriqui, Panama, 22 Feb 1934, sta 251 ��� 34, coll. W.L. Schmitt, 27 m, USNM 1253253; 4 males (SL 1.0��� 1.9 mm), 12 females (SL 1.2���2.4 mm), 1 ovig female (SL 1.5 mm), Parker Bay, Costa Rica, 9 Feb 1935, R/V Velero III, sta 468 ���35, 9 m, USNM 1253254; 2 males (SL 1.3���1.6 mm), Salinas Bay, Costa Rica, 11 Feb 1935, R/V Velero III, sta 481 ���35, 11 m, USNM 1253255. SCRIPPS holdings: 24 NS, in shell, Bah��a Banderas, Mexico, 20 �� 41 'N, 105 �� 23.5 'W, 21 Aug 1961, sta 610813 ��� 52, coll. F.H. Berry, 63���65 m, SIO C- 2441; 1 male (SL 2.0 mm), Golfo de Fonseca, El Salvador, 13 ��01.1'N, 88 ��01.7'W, 4 Apr 1978, B/O ���A. Helix'', sta TEPE 78 ��� 9, coll. J. Lance, ot, 42 m, SIO C- 4085. Diagnosis. Shield about as long as broad; rostrum broadly subtriangular, blunt, not reaching tip level of lateral projections or basis of ocular acicles. Ocular peduncles long, slender, straight, cornea weakly dilated. Antennal flagellum with numerous long setae directed ventrally. First maxilliped without epipod. Third maxillipeds with endopod-exopod joint moderately separated. Carpus and palm of chelipeds each with 5 strong spines on dorsomesial margin. Propodus of second pereopods with row of 5���7 spines on dorsal margin. Redescription. Shield (Fig. 1 A) about as long as broad, dorsal surface with few small spines anteriorly, short transverse rows of small spines mostly near anterolateral margins, and scattered tufts of short setae; rostrum blunt, broadly subtriangular, not reaching tip level of lateral projections or basis of ocular acicles, upper surface somewhat concave; lateral projections obtuse, exceeding rostrum in distal extension, ending in marginal spine. Posterior margin rounded. Anterolateral angles each with 1 moderately strong spine. Branchiostegites each with row of spinules on dorsomesial and distal margins, concealed partially by tufts of long setae. Ocular peduncles (Fig. 1 A) long, slender, slightly compressed medially, about 0.90 length of shield. Ocular acicles subtriangular, terminating in strong spine, separated by approximately 0.33 basal width of 1 acicle. Antennular peduncles (Fig. 1 A) long, distal segment overreaching ocular peduncles by 0.50 length of ultimate segment. Ultimate and penultimate segments unarmed, with some tufts of setae on ventral and dorsal margins. Basal segment with 1 small spine on distal ventromesial margin, 1 small spine on laterodistal margin, and 1 moderately strong subdistal spine on lateral margin. Antennal peduncles (Fig. 1 A) with supernumerary segments, overreaching distal margin of corneas by about 0.33 of fifth segment. Fifth segment unarmed, with few short setae on ventrolateral margin and dorsal surface. Fourth segment with small dorsodistal spine. Third segment with 1 strong or moderately strong spine on ventromesiodistal angle and tufts of long setae. Second segment with dorsolateral distal angle moderately to strongly produced, ending in single spine; lateral margin unarmed; dorsomesial distal angle ending in strong spine, mesial margin with tufts of setae. First segment with ventrodistal margin produced, with 1 moderately strong laterodistal spine. Antennal acicle nearly straight, approximately 0.25 length of antennal peduncle, mesial margin armed with 2���4 spines, lateral margin with 2 small spines or spinules subdistally, ending in bifid spine. Antennal flagella long, approximately 1.50 length of shield, consisting of about 21 articles and reaching to tip of cheliped fingers when totally extended, ventrally with rows of long setae 3���6 flagellar articles in length. Mandible without distinguishing characters. Maxillule (Fig. 2 A) with proximal endite subquadrate, distal endite subrectangular, enlarged distally; endopod with 1 proximal seta, 3���5 stout setae or bristles on weakly produced internal lobe, external lobe well developed, recurved, approximately 0.75 length of endopod, external angle with 7 long setae. Maxilla (Fig. 2 B) with endopod moderately long, extending to distal margin of scaphognathite, somewhat inflated basally. First maxilliped (Fig. 2 C) with endopod elongate, approximately 0.70 length of basal segment of exopod, strongly twisted; flagellum short, unsegmented, with long, marginal plumose setae distally; epipod absent. Second maxilliped (Fig. 2 D) with basis-ischium fusion incomplete. Third maxilliped (Fig. 2 E) with joint of endopod and exopod moderately separated; basis-ischium fusion incomplete; coxa with 3 or 4 small spines distally concealed partially by long setae; basis usually with 2 or 3 small spines; ischium with crista dentata well developed, with 10���12 teeth, without accessory tooth, usually with 1 small spine on dorsodistal margin; merus with 1 or 2 spines on ventrolateral margin, dorsodistal margin with 1 small spine; carpus, propodus and dactyl unarmed. Chelipeds subequal, right slightly longer than left, similar in armature (Fig. 3 A, B). Dactyls each about 1.75 times longer than palms; dorsomesial margin with row of strong, corneous-tipped spines decreasing in size distally and accompanied with tufts of long setae; dorsal surface with 2 irregular longitudinal rows of corneous-tipped spines accompanied by tufts of long setae; mesial surface with 2 irregular longitudinal rows of spines, upper largest; ventral surface with scattered tufts of long setae; cutting edge with small calcareous denticles interspaced with small corneous spines; terminating in an acute corneous claw overlapped by fixed finger. Palms each about 0.80 length of carpi; dorsomesial margin armed with 5 prominent, corneous-tipped conical spines accompanied with tufts of long setae; dorsolateral margin armed with small, corneous-tipped spines or tubercles, more numerous on fixed finger; dorsal surface with 4 or 5 irregular longitudinal rows of corneous-tipped spines smaller than on dorsomesial margin, each accompanied by tufts of long setae; mesial surface nearly straight, with scattered granules or tubercles, larger near dorsal margin and accompanied by long setae; lateral surface slightly convex, with few small spines accompanied by tufts of long setae; ventral surface with few spines or tubercles extending on fixed finger. Fixed finger ending in small corneous claw; dorsal surface with 2 or 3 irregular longitudinal rows of corneous-tipped spines accompanied by tufts of long setae. Carpi short, each about 0.80 length of meri, subquadrate in cross-section; dorsomesial margin with 5 or 6 strong, corneous-tipped spines increasing in size distally; dorsolateral margin with 4 or 5 small spines; dorsal surface flat, with few tufts of long setae; mesial and lateral surfaces with few flattened granules or tubercles accompanied by tufts of long setae; ventrolateral distal angle with 1 or 2 moderately strong spines. Meri triangular in cross-section; dorsal surface with small granules partially concealed by tufts of long setae; distal and subdistal margins each armed with 1 large corneous-tipped spine; ventromesial and ventrolateral margins spinose, with larger spines on mesial margin; mesial surface smooth; external surface with few small granules and tufts of long setae. Ischia each with row of small spines on ventromesial margin; ventrolateral distal angle with 1 moderately strong spine. Second (Fig. 3 C) and third (Fig. 3 D) pereopods slender, similar right from left except slightly in armature, exceeding to chelipeds by approximately 0.50 of dactyls length when totally extended. Dactyls each 1.30���1.40 times length of propodi; dorsal surface with double row of tufts of long setae; mesial and lateral surfaces each with median longitudinal row of setae, longer on mesial surface; ventromesial and ventrolateral margins and ventral surface each with row of tufts of long setae. Propodi 1.28���1.30 times length of carpi; dorsal surface with row of 5���7 moderately strong spines (second, spines weakly developed and less in number in specimens SL ��� 2.0 mm), or 1 anterior and 1 posterior (third) and tufts of long setae; mesial surface usually with 2 longitudinal rows of long setae; lateral surface with shallow longitudinal sulcus and usually 2 rows of long setae; ventral surface with 1 irregular (second) or 2 rows (third) of small, spiniform granules accompanied by tufts of short setae. Carpi each 0.77���0.88 times length of meri; dorsal surface with 1 row of spines (second), or 1 or 2 small spines (third), 1 distal and 1 posterior, and tufts of long set, Published as part of Ay��n-Parente, Manuel, Hendrickx, Michel E. & Lemaitre, Rafael, 2015, Redescription and taxonomic status of Paguristes praedator Glassell, 1937 and P. oxyophthalmus Holthuis, 1959 (Anomura: Paguroidea: Diogenidae), with an emendation to the diagnosis of the genus Areopaguristes Rahayu & McLaughlin, 2010, pp. 491-509 in Zootaxa 3915 (4) on pages 494-501, DOI: 10.11646/zootaxa.3915.4.2, http://zenodo.org/record/234099, {"references":["Glassell, S. A. (1937) The Templeton Crocker Expedition. XI. Hermit crabs from the Gulf of California and the west coast of Lower California. Zoologica, 22, 241 - 263.","Haig, J., Hopkins, T. S. & Scanland, T. B. (1970) The shallow water anomuran crab fauna of southwestern Baja California, Mexico. Transactions of the San Diego Society of Natural History, 16 (2), 13 - 32.","Moran, D. A. & Dittel, A. I. (1993) Anomuran and brachyuran crabs of Costa Rica: annotated list of species. Revista de Biologia Tropical, 41, 599 - 617.","Garcia-Madrigal, M. S. (1999) Anomuros (Anomura) del arrecife de Cabo Pulmo-Los Frailes y alrededores, Golfo de California. Revista de Biologia Tropical, 47 (4), 923 - 928.","Hendrickx, M. E. & Harvey, A. W. (1999) Checklist of anomuran crabs (Crustacea: Decapoda) from the eastern tropical Pacific. Belgian Journal of Zoology, 129, 363 - 389.","Boschi, E. E. (2000) Species of decapod crustaceans and their distribution in the American marine zoogeographic provinces. Revista de Investigacion y Desarrollo Pesquero, 13, 7 - 136.","Vargas, R. & Cortes, J. (2006) Biodiversidad Marina de Costa Rica: Crustacea: Infraorden Anomura. Revista de Biologia Tropical, 54 (2), 461 - 488. http: // dx. doi. org / 10.15517 / rbt. v 54 i 2.13894","Rodriguez de la Cruz, M. C. (1987) Crustaceos decapodos del Golfo de California. Secretaria de Pesca (Ed.), Mexico, D. F., 306 pp.","Ayon-Parente, M. & Hendrickx, M. E. (2010 a) Species richness and distribution of hermit crabs of the family Diogenidae (Crustacea: Decapoda: Anomura) in the eastern Pacific. Nauplius, 18 (1), 1 - 12.","Hinds, R. B. (1843) Descriptions of new shells, from the collection of Captain Sir Edward Belcher, R. N., C. B. & C. Proceedings of the Zoological Society of London, part 11, 36 - 46. http: // dx. doi. org / 10.1080 / 03745484309445298","Hinds, R. B. (1844) The Zoology of the voyage of H. M. S. Sulphur, under the command of Captain Sir Edward Belcher, R. N., C. B., F. R. G. S., etc. during the years 1836 - 1842. Vol. II. Smith, Elder and Co., London, 72 pp., 21 pls.","Dall, W. H. (1908) Reports on the dredging operations off the west coast of Central America to the Galapagos, to the west coast of Mexico, and in the Gulf of California, in charge of Alexander Agassiz, carried on by the U. S. Fish Commission steamer \" Albatross \" during 1891, ... XXXVIII. Reports on the scientific results of the expedition to the eastern tropical Pacific in charge of Alexander Agassiz, by the U. S. Fish Commission steamer \" Albatross \", from October, 1904, to March, 1905, .. XIV [concerning: Kabat (1996)]. Harvard College [University]. Bulletin of the Museum of Comparative Zoology, 43 (6), 205 - 487.","Berry, S. S. (1960) Notes of new eastern Pacific Mollusca - IV. Leaflets in Malacology, 1 (23), 139 - 146.","Reeve, L. A. (1843) Conchologica Iconica, or, Illustrations of the Shells of Molluscous Animals. Vol. I. Containing Monographs of the Genera ... Pleurotoma ... London, King William Street, Strand. [Real printing dates various months in 1845 and 1846].","King, P. P. & Broderip, W. J. (1832) Description of the Cirripedia, Conchifera and Mollusca in a collection formed by the officers of HMS Adventure and Beagle employed between the years 1826 and 1830 in surveying the southern coasts of South America, including the strait of Magallanes and the coast of Tierra del Fuego. Zoological Journal, 5, 332 - 349.","Dall, W. H. (1910) Description of a new genus and species of bivalve from the Coronado Islands, Lower California. Proccedings of the Biological Society of Washington, 23, 171 - 172."]}

Typton granulosus sp. nov. Figs. 1���5 Material examined. Holotype: female (pocl/cl 1.8 / 2.2 mm), Isla Colorada, Bah��a Chamela, Jalisco, Mexico, 19 �� 32��24 ����N 105 �� 5��32 ����W, 7 m, Scuba, 12 Nov 2013, LEMA CR- 463. Paratypes: 1 female (pocl/cl 1.8 / 2.2 mm), same data, LEMA CR- 464. 1 ovigerous female (pocl/cl 2.1 / 2.5 mm), Barra de Navidad, 19 �� 11��24 ����N 104 �� 41��38 ����W, low intertidal, 11 Sep 1982, EMU- 8828. 2 ovigerous females (pocl/cl 2.2���2.8 / 2.6���3.3 mm), off R��o Suchiate, Gulf of Tehuantepec, 14 �� 21��48 ����N 92 �� 34��24 ����W, 64 m, 13 May 1992, EMU- 8842. Description. Carapace (Fig. 1 A���F) slightly compressed, glabrous, smooth, longer than wide. Rostrum short, simple, triangular, about 0.45 length of ocular peduncle, slightly curving upward; paraorbital processes well developed, usually slightly exceeding the rostrum and reaching anterior margin of the cornea in lateral view, exceeding by half of its length level of anterior pterygostomial margin, weakly divergent in dorsal view, pointing slightly upward in lateral view. Orbit feebly demarcated, without distinct inferior orbital angle or antennal spine; pterygostomial margin slightly produced anteriorly, rounded to somewhat angular. Eyes (Fig. 1 A���F) well developed, cornea rounded, weakly dilated, obliquely set on stalk; inner margin of stalks straight; anterior margin of cornea reaching distal third of first segment of the antennular peduncle. Abdomen (Fig. 1 A, D) elongated, smooth, glabrous, about 2.5 times CL; first to fourth somites with broadly rounded pleura, fifth bluntly angular; sixth segment 0.25 of CL, posterolateral angle spiniform, posterodorsal margin (Fig. 1 G) without median tooth; fifth and sixth segments subequal in length; first to sixth sternites unarmed. Telson (Fig. 1 G) moderately slender, tapering, about 2.5 times length of sixth somite, 2.5 times longer than wide; lateral margins convex, converging to a broad, rounded posterior margin; dorsal surface with two pairs of well-developed spines, each about 0.14 times telson length, approximately at 0.1 and 0.5 of telson length; 3 pairs of posterior spines, lateral pair minute, intermediate pair long, slender, plumose, about 0.15 of telson length, median pair as long as intermediate, slightly stouter, one simple seta between median and intermediate spines. Antennular peduncle (Fig. 2 A) slender, proximal article subcylindrical, 3.3 times as long as distal width; statocyst well-developed, with statolith; stylocerite acute, short, about 0.1 times length of article; intermediate article shorter than distal article, their combined length equal to about 0.4 of proximal article length; lateral (= superior) flagellum short, stout, with 8���9 groups of aesthetascs, short ramus distally, longer ramus with 5���6 segments; mesial (= lower) flagellum long, with 9���10 segments. Antenna (Fig. 2 B) basicerite stout, unarmed, conspicuous antennal gland tubercle medially; carpocerite slender, subcylindrical, reaching distal margin of intermediate antennular peduncular segment, about 8 times as long as wide, 2.3 times merocerite length, flagellum slender, short, about 4 times carpocerite length; scaphocerite reduced, about 0.4 carpocerite length, 3 times as long as proximal width, tapering distally, terminally rounded, without distolateral spine or setae. Mandibles (Fig. 2 C, D) with slender corpus, without palp; molar processes slender, tapering, obliquely truncate distally, left with several spines, right distally acute, with two stout processes; incisor process slender, tapering, obliquely truncate distally, with 6 (left) and 7 (right) small acute teeth. Maxillula (Fig. 2 E) palp bilobed, upper lobe reduced, lower lobe larger, with long slender, simple terminal seta; upper lacinia well developed, 1.3 times longer than broad, distal margin with double row of about 10 stout, denticulate spines, and 8 plumodenticulate setae; lower lacinia slender, tapering distally, distal setae spiniform, ventral setae plumose. Maxilla (Fig. 2 F) with short slender, non-setose palp; basal endite well developed, bilobed, upper lobe larger and broader than lower, lobes each with about 13 slender, feebly setulose setae; coxal endite obsolete; scaphognathite well developed, slender, 4 times longer than width at mid length, with marginal plumose setae, anterior lobe 2.5 times longer than wide, medially concave. First maxilliped (Fig. 2 G) with short tapering palp, one subterminal simple seta; basal endite large, densely spinulated medially, spines minutely denticulate; coxal endite reduced, non setose; exopod with well-developed setose caridean lobe, flagellum slender, with single long simple terminal setae; epipod bilobed. Second maxilliped (Fig. 2 H) dactylar article broad, 3 times longer than maximal width, densely spinose medially, spines robust, minutely denticulate; propodal article distomedially rounded, not produced, marginal spines similar to dactyl; carpus, merus, and ischio-basis without special features; exopod flagellum slender, four long plumose terminal setae; epipod (Fig. 2 I) subrectangular. Third maxilliped (Fig. 2 J) antepenultimate article broad, penultimate article twice as long as ultimate, 0.6 times as long as the antepenultimate article; exopod reaching slightly beyond anterior margin of antepenultimate article, two short simple, subdistal setae, four slender plumose, distal setae. First pereiopods (Fig. 3 A, B) exceeding second minor pereiopod by length of the palm. Palm of chela slender, swollen in appearance, subcylindrical, slightly compressed, about 2.5 times as long as wide. Fingers robust, short and stout, about 0.45 of palm length, strongly spatulate, cutting edges entire, that of dactyl thicker, tip with three small stout teeth, fixed finger tip with three teeth, cutting edge thin, outer and mesial surfaces of fingers bearing some tufts of serrulate setae. Carpus about 4.7 times longer than wide, about 1.8 times as long as palm, tapering proximally. Merus slender, about 6.4 times longer than broad, 1.3 times as long as carpus. Ischium short, stout, broader than merus, about 3 times as long as broad, 0.6 times length of merus. Basis shorter and more slender than ischium. Second pereiopods unequal. Major pereiopod (Fig. 3 C, D) exceeding minor cheliped by length of dactyl. Palm of chela stout, slightly compressed, about twice as long as wide; mesial surface with small, triangular, spiniform granules, which extend on lower and upper margins. Fingers robust, short, stout, spatulate, about 0.67 width of palm. Dactyl with cutting edge entire, tip terminating in a corneous claw. Fixed finger with proximal molar tooth ending in corneous claw, outer and mesial surfaces of fingers with numerous tufts of setae. Carpus stout, short, 1.2 times longer than broad, strongly extended distally, ventro-mesial angle with 1 to 2 denticles. Merus short, stout, 1.5 times longer than broad, slightly shorter than carpus, dorsal and ventral margins convex, ventral margin bearing small acute tubercles. Ischium about twice longer than broad, slightly longer than merus. Minor second pereiopod (Fig. 3 E���G) with palm about 1.8 times longer than maximal depth, oval in section, converging distally, with small, triangular, spiniform granules on mesial surface and dorsal and ventral margins, dactyl spatulate, compressed, about 0.4 of palm length, 1.75 times longer than maximal depth, dorsal margin curved with some tufts of long setae, cutting edge almost straight, entire, with subdistal concavity, ending in strong tooth; fixed finger about twice longer than proximal width, cutting edge deeply grooved, medial flange sharp, entire, lateral flange broadly triangularly expanded; carpus 0.4 of carpal length palm, smooth, about 1.5 times as long as maximal height, much wider distally; merus 1.5 times as long as broad, about 0.9 of carpal length and 0.4 of palm length, with small conical teeth on ventral surface; ischium about 1.5 times length of merus, unarmed. Third pereiopod (Fig. 4 A���C) stout, reaching distal margin of carpus of major cheliped. Dactyl biunguiculate, compressed, about 0.3 propodus length and twice longer than its basal width, ventral margin of corpus slightly concave, crenulate, with acute, triangular, ventrally pointing secondary unguis; terminal unguis distinctly demarcated, about half as long as corpus, strongly curved, not crenulated proximally; propodus about 3.3 times as long as wide, ventral margin with 2���5 irregularly spaced spines, distal pair of stouter spines fringing base of dactylus; carpus about 0.9 length of propodus, nearly 3 times as long as distal width, unarmed; merus about twice as long as broad and 1.3 times length of carpus, unarmed; ischium about 0.9 times length of merus, unarmed. Fourth pereiopod (Fig. 4 D) similar to third; dactyl biunguiculate, twice as long as basal width; ventral margin corpus conspicuously crenulated, with triangular, ventrally pointing secondary unguis; terminal unguis equal or slightly shorter than half-length of corpus; propodus about 3.5 as long as wide; ventral margin with 1 to 3 spines and distal pair of stouter spines; carpus slightly shorter than propodus, about 2.5 times as long as distal width; merus about 2.5 times as long as wide; ischium about as long as merus, 2.5 times longer than distal width. Fifth pereiopod (Fig. 4 E, F) more slender than third and fourth, with dactyl biunguiculate, compressed, about 0.3 of propodus length, 2.5 times as long as basal width, unguis well demarcated, about 0.67 of corpus length, 2.5 times longer than basal width, curved, crenulated proximally, corpus 1.3 times longer than basal width, with dorsal and ventral margins slightly convex, ventral margin crenulated, with strong, subacute, ventrally pointed secondary unguis; propodus about 6 times as long as broad; ventral margin with one subdistal and one distal spine, distal 0.3 with brush of grooming setae; carpus 0.7 times length to propodus, about 2.5 times as long as distal width, unarmed; merus about 3.6 times as long as wide and 1.4 length of carpus, unarmed; ischium about 0.7 length of merus, unarmed. First female pleopod (Fig. 5 A) endopod reaching half-length of exopod, margins with long plumose setae. Second female pleopod (Fig. 5 B) 0.9 length of exopod; appendix interna (Fig. 5 C) inserted at mid-length of mesial margin, with long, lateral plumose seta and 8 subdistal cincinnuli. Uropods protopod (Fig. 1 G) unarmed; exopod (Fig. 1 G) oval, slightly longer than telson, outer margin nonsetose, distolateral margin (Fig. 5 D���I) serrate in distal third, with 5���9 acute or subacute teeth, distolateral angle with acute tooth, reaching approximately half-length of stout, terminal spine; diaeresis inconspicuous; endopod (Fig. 1 G) slightly longer than exopod, proximal parts of lateral and mesial margins non-setose. Numerous ova, suboval, with mean diameter 0.4 mm. Variation. The most obvious variable character are the paraorbital processes, which can reach the basis of the cornea (Fig. 1 A���E) or half of the ocular peduncle length (Fig. 1 F). The pterygostomial region varies from broadly rounded (Fig. 1 C���E) to more angularly protruding (Fig. 1 F). The number of spines on the ventral margin of the propodi in the third and fourth pereiopods vary from 2 to 5 and from one to 3, respectively. There is also a significant variation in the number of teeth on the distolateral margin of the uropodal exopod, ranging from 5���9 (not including terminal tooth adjacent to strong spine), and in the number of mobile spines adjacent to terminal tooth, ranging from 1 to 3 (Fig. 5 D���I). Type locality. Isla Colorada, Bah��a Chamela, Jalisco, Mexico. Etymology. The name of the species is derived of the latin granum (grain), which makes reference to the minute granules present on the mesial surface of the major second pereiopod. Distribution. Known from Bahia Chamela and Barra de Navidad, Jalisco, and off R��o Suchiate, Gulf of Tehuantepec, Chiapas, Mexico. Ecology. The specimens of Typton granulosus sp. nov. from Bah��a Chamela were collected on Holothuria (Halodeima) inornata Semper, 1868 (Echinodermata: Holothuridae), a tropical species commonly found in the Mexican Pacific and distributed from the Gulf of California to Ecuador (Sol��s-Mar��n et al. 2009). The sea cucumber was found in a mixed sand-rubble bottom area near Isla Colorada. Typton granulosus sp. nov. probably lives in association with this holothurid. Other species of Typton (e.g., T. tortugae and T. wasini Bruce, 1977) are known to be commensal of sponges (Bruce 1978, 1987). Remarks. Typton granulosus sp. nov. is close to Typton serratus from the eastern Pacific, T. holthuisi from the central Atlantic, T. spongicola from the eastern Atlantic, and T. fapespae and T. prionurus, both from the west Atlantic. These five species have the distal part of the outer margin of the uropodal exopod serrated. Typton granulosus sp. nov. can be easily separated from T. holthuisi, T. fapespae, and T. spongicola by the absence of a strong median tooth on the posterodorsal margin of the sixth abdominal somite (De Grave 2010, Fig. 1 D; Almeida et al. 2014, Fig. 1 F; Bruce 2009, Fig. 3 J), the rostrum is shorter than the paraorbital processes, and the number of teeth on the distolateral margin of uropods is higher [5���9 vs. 3���4 in T. holthuisi (De Grave 2010, Fig. 1 K, L), 2���6 in T. fapespae (Almeida et al. 2014, Fig. 3 I���L), and 3 in T. spongicola (Bruce 2009, Fig. 2 D, E)]. Given the morphological similarity of Typton granulosus sp. nov. and T. prionurus, they can be considered sister species occurring on both sides of the American continent. Typton granulosus sp. nov. can be distinguished from T. prionurus by a proportionally shorter rostrum in relationship to the ocular peduncles length, and by the fact that the antennal peduncle reaches the distal margin of the penultimate antennular segment in lieu of the antennal peduncle reaching the end of the antennular peduncle (Holthuis 1951, Fig. 52 a, b); the palm of the major cheliped is proportionally longer than wide (twice vs. 1.67 times) and the carpus is shorter in relation to the chela (0.25 vs. 0.4) in T. granulosus; the mesial surface of the palm of the major and minor chelae of T. granulosus bears minute, triangular, spiniform granules which are absent in the Atlantic species. Typton granulosus sp. nov. also differs from T. serratus by the size of the rostrum, proportionally longer than the paraorbital processes in the latter (Holthuis 1951, Fig. 53 b); also, the palm of the major cheliped is slightly convex on dorsal and ventral margins in Typton granulosus sp. nov., while in T. serratus those margins are straight (Holthuis, 1951, Fig. 53 i); the serration of the uropodal exopod is confined to the distal third in T. granulosus while the serrated region is much larger in T. serratus; finally, the pair of dorsal spines on the telson is widely separated in T. granulosus vs. closely set together, in the anterior quarter of the telson, in T. serratus (Holthuis 1951, Fig. 53 c). Typton granulosus sp. nov. can be easily distinguished from all other eastern tropical Pacific species of Typton by the presence of a serration on the laterodistal margin of the uropodal exopod., Published as part of Ay��n-Parente, Manuel, Hendrickx, Michel E. & Galvan-Villa, Cristian Moises, 2015, A new species of the genus Typton Costa (Crustacea: Decapoda: Palaemonidae: Pontoniinae) from the eastern tropical Pacific, pp. 430-438 in Zootaxa 3926 (3) on pages 431-437, DOI: 10.11646/zootaxa.3926.3.7, http://zenodo.org/record/231841, {"references":["Solis-Marin, F. A., Arriaga-Ochoa, J. A., Laguarda-Figueras, A., Frontana-Uribe, S. C. & Duran-Gonzalez, A. (2009) Holoturoideos (Echinodermata: Holothuroidea) del Golfo de California. CONABIO & ICMYL-UNAM, Mexico D. F., 177 pp.","Bruce, A. J. (1978) Typton crosslandi sp. nov., a new pontoniine shrimp from the Galapagos Islands. Crustaceana, 35 (3), 294 - 300. http: // dx. doi. org / 10.1163 / 156854078 X 00448","Bruce, A. J. (1987) Typton nanus sp. nov., a new commensal shrimp (Crustacea: Decapoda: Palaemonidae) from the Australian North-West shelf. Records of the Northern Territory Museum of Arts and Sciences, 4 (1), 49 - 56.","De Grave, S. (2010) A new species of the genus Typton Costa (Decapoda, Palaemonidae, Pontoniinae) from Ascension Island. In: Fransen, C. H. J. M., De Grave, S. & Ng, P. K. L. (Eds.), Studies on Malacostraca: Lipke Bijdeley Holthuis Memorial Volume. Crustaceana Monographs, 14, pp. 209 - 218. [Brill, Leiden]","Almeida, A. O., Anker, A. & Mantelatto, F. L. (2014) A new snapping species of the shrimp genus Typton Costa, 1844 (Decapoda: Palaemonidae) from the coast of Sao Paulo, southeastern Brazil. Zootaxa, 3835 (1), 110 - 120. http: // dx. doi. org / 10.11646 / zootaxa. 3835.1.6","Bruce, A. J. (2009) A re-description of Typton spongicola Costa, 1844, the type species of the genus Typton Costa, 1844 (Crustacea: Decapoda: Pontoniinae). Cahiers de Biologie Marine, 50, 383 - 394.","Holthuis, L. B. (1951) A general revision of the Palaemonidae (Crustacea Decapoda Natantia) of the Americas. I. The subfamilies Euryrhynchidae and Pontoniinae. Allan Hancock Foundation Publications of the University of Southern California, Occasional Paper, 11, 1 - 332."]}

Caprella suprapiscis sp. nov. (Figures 1���5) Type material. Holotype male. Bah��a Chamela, Isla Cocinas. 19 �� 32��46 ����N, 105 ��06��28 ����W, 6 m depth, 10 October 2013, collected from Scorpaena mystes, coll. Cristian M. Galv��n-Villa and Valentina Fern��ndez-Del Valle (LEMA- CCR 454 A). Paratypes. Same locality. Same date. 1 female (LEMA-CCR 454 B); 1 male (LEMA-CCR 454 C); 1 female (LEMA-CCR 454 D); 1 male (LEMA-CCR 457 B). Bah��a Chamela, Isla Pajarera. 19 �� 33��44 ����N, 105 ��06��42 ����W, 6 m depth, 0 6 December 2013, 1 male and 1 female (EMU); 1 male and 1 female (CNCR); 1 male and 1 female (LACM-CR); 1 male and 1 female (USNM). Additional material. Bah��a Chamela, Isla Colorada. 19 �� 32��23 ����N, 105 ��05��31 ����W, 6 m depth, 10 October 2103, 1 male, 3 females, and 1 juvenile (LEMA-CCR 451); 5 m depth, 10 October 2013, 1 male and 1 female (LEMA-CCR 452); 7 m depth, 12 November 2013, 40 males, 32 females, and 37 juveniles (LEMA-CCR 456). Bah��a Chamela, Isla Cocinas. 19 �� 32��46 ����N, 105 ��06��28 ����W, 5 m depth, 10 October 2013, 1 female (LEMA- CCR 453); 6 m depth, 10 October 2013, 27 males, 21 females, and 31 juveniles (LEMA-CCR 454). Bah��a Chamela, San Agust��n. 19 �� 32��8 ����N, 105 ��05��15 ����W, 5 m depth, 12 October 2013, 2 males (LEMA-CCR 455). Bah��a Chamela, Isla Pajarera. 19 �� 33��44 ����N, 105 ��06��42 ����W, 6 m depth, 0 6 December 2013, 56 males, 24 females, and 12 juveniles (LEMA-CCR 457 A). Type locality. Isla Cocinas, Bah��a Chamela, Jalisco, Mexican Pacific. Distribution in the area. The Bah��a Chamela islands were declared a Natural Protected Area since 2002 with the category of Sanctuary. Eight islands (Pajarera, Cocinas, Mamut, Colorada, San Pedro, San Agust��n, San Andr��s, and Negrita) and four islets (Los Anegados, Novillos, Mosca, and Submarino) are included. So far Caprella suprapiscis sp. nov. has been collected in Cocinas, Colorada, San Agust��n, and Pajarera islands (Fig. 1). Etymology. The species name suprapiscis is derived of the Latin supra (over) and piscis (fish), referring to the presence of the caprellids on the skin of Scorpaena mystes. Description. Based on the male holotype (LEMA-CCR 454 A). Body length. 6.1 mm. Lateral view. Body dorsally slender without tubercles or spines. Head with a forward-pointing dorsal projection (shorter in females and juveniles), head and pereonite 1 partially fused, suture present. Pereonites 1���2 similar in length and larger than 3���6, pereonite 7 the shortest. Pereonite 5 with a small mid-dorsal projection (Fig. 2 A, C, D). Gills. Present on pereonites 3���4, elongate, length about 3.5 times width (Fig. 2 A). Antennae. Antenna 1 about half of the body length; peduncle scarcely setose; peduncular article 2 longest, 1.6 times length of article 1; peduncular articles 1���3 with numerous small granules and some short setae; flagellum composed of 15 articles. Antenna 2 about half length of antenna 1; peduncular articles carrying 12 pairs of long setae; flagellum 2 -articulate with serrate setae (Fig. 2 B, C). Penes. Short, length about 1.5 times the width. Abdomen with a pair of 2 -articulate appendages, bearing 5 setae on basal article and 2 on distal article; a pair of lateral lobes and a single dorsal lobe (Fig. 3 D). Mouthparts. Maxilliped inner plate with 2 teeth and 6 simple setae; outer plate with 5 robust and short setae and 13 simple marginal and submarginal setae; palp 4 -articulate, setose; article 4 with rows of setulae on grasping margin (Fig. 4 A). Maxilla 1 outer lobe with 7 forked spines; palp biarticulate; article 2, 4 times article 1, with 8 teeth distally, 5 robust subdistal and 5 lateral setae (Fig. 4 B). Maxilla 2 inner lobe oval, outer lobe rectangular, about 2.4 times as long as the inner lobe (Fig. 4 C). Upper lip symmetrically bilobed, short setae apically (Fig. 4 D); lower lip with inner lobes well demarcated; inner and outer lobes with short setae (Fig. 4 E). Mandibular molar process strong; incisor and lacinia mobilis 5 toothed; left mandible with 3 pectinated setae, right mandible with only 2 (Fig. 4 F, G). Gnathopods. Gnathopod 1 basis as long as ischium, merus, and carpus combined, with 4 long setae subdistally; 3 ventral setae on ischium; merus and carpus setose; propodus elongate, length about 2 times width; propodus palm with 2 proximal grasping spines, grasping margin serrate, with mixed long and short setae along the palm, two longitudinal rows of setae, one near grasping margin, another near dorsal margin, latter longer; dactylus slightly curved, grasping margin serrate, with few setae, one large tooth subdistally; middle outer surface with row of moderately strong teeth on distal third, becoming flattened scales posteriorly, middle upper outer surface with 5���6 longitudinal rows of flattened scales bearing short, marginal setae (Fig. 5 A). Gnathopod 2 inserted near distal end of pereonite 2; basis about 1.7 times the length of pereonite 2 and 3 / 5 length of propodus, provided with a dorsal projection, dorsal margin finely setose; ischium subrectangular; merus with tuft of setae ventrally; carpus very reduced, subtriangular; propodus elongate, length about 3 times width, dorsal surface slightly convex and finely setose on dorsal and ventral margins with one proximal projection provided with a robust seta from 2 / 5 of proximal end; another projection in the middle, followed by ���U��� notch distally; dactylus falcate, setose on dorsal and lateral margins, with a proximal broad tooth followed by a smaller tooth; flexor margin with minute granules (Fig. 5 B). Pereopods. Pereopods 3 and 4 absent. Pereopods 5���7 increasing in length, scarcely setose; basis with a distal triangular projection; basis of pereopods 6 and 7 with small granules on dorsal margin; merus with a rounded projection and some setae; carpus subrectangular, nearly as long as merus, with setae at dorsal and ventral margins; propodus provided with a pair of grasping spines proximally; dactylus curved (Fig. 6). Paratype female. LEMA-CCR 454 B. Differs from male in the following characters: flagellum of antenna 1 with 12 articles (Fig. 3 A); head with forward-pointing dorsal spine shorter than male; oostegites present. Gnathopod 2 inserted on the anterior half of pereonite 2, basis about half of pereonite 2 length; propodus length about 2 times width and 2.5 times longer than basis; dorsal surface of propodus convex with 3 setae; with only one anteriorly ventral projection provided with a robust bifid seta from 1 / 4 of proximal end; margin ventral with numerous robust bifid and single setae; mid-palmar projection followed by a minute sinus and a small triangular projection. Dactylus ventrally granulate (Fig. 5 C). Pereonites 2 and 3 about the same length, longer than pereonites 4 and 5. Pereonites 3 and 4 with small tubercle on dorsal margin. Pereonite 5 with a pair of genital papillae. Abdomen without appendages, only lateral and dorsal lobes presents (Fig. 3 B, C). Color in life. Color differs according to the location of the specimens on the body surface of the fish, thus indicating a mimetic adaptation. Remarks. Specimens of C. suprapiscis sp. nov. were collected from seven scorpionfishes (Scorpaena mystes) in coral and rocky reefs habitats in depths between 5 and 7 m. This is the first record of a caprellid associate with fishes in the eastern Pacific and the second worldwide (Mori & Yamato 1993). When compared to other species reported for the eastern Pacific, Caprella suprapiscis sp. nov. presents major resemblance with C. californica Stimpson, 1857, C. mercedesae Hendrickx & Ay��n-Parente, 2014, and C. scaura Templeton, 1836 that also feature a sharp spine on the forehead. Besides, C. suprapiscis sp. nov. and C. californica have setose second gnathopods. Caprella suprapiscis sp. nov. is distinguished from C. californica by the shorter rostrum, fewer number of articles in antenna 1 (15 vs. 20), the maxilliped inner plate with 2 teeth and the outer plate with 5 teeth, in lieu of 3 teeth and only setae (no teeth), respectively, and maxilla 1 with article 2 shorter, ventral margin of gnathopod 1 serrated vs. unserrated, gnathopod 2 proportionally shorter in the relation lengthwide and shorter basis length, absence of a dorsal and a ventral projections in pereonite 2 in both males and females, and absence of a pair of mid-dorsal projections on pereopods 6 and 7. The new species C. suprapiscis is also clearly smaller than C. californica. The largest male of C. suprapiscis was 9 mm, whereas C. californica maximum length is 24.23 mm (Takeuchi & Oyamada 2013). Caprella suprapiscis sp. nov. can be differenced of C. mercedesae by the position of the rostral spine, behind the eyes in the former vs. anterior to the eyes in the later; the dactyl of gnathopod 1 ends in a single tooth in C. suprapiscis but bears 4 large teeth in C. mercedesae; in males, gnathopod 2 is set at the posterior margin of pereonite 2 vs. at mid-length in C. mercedesae, the carpus is unarmed in the new species and its ventral margin is serrate in C. mercedesae; the dactyl is smooth in the new species vs. finely crenulated dorsally in C. mercedesae, pereonites 5 to 7 lack spines in C. suprapiscis sp. nov. but bear spines on the posterior margin in C. mercedesae. Finally, Caprella suprapiscis sp. nov. can be distinguished from C. scaura in which the forehead spine is located further from the eyes (Templeton, 1836, fig. 6 a, b) than in C. suprapiscis; also, the basis of gnathopod 2 is proportionally larger in C. scaura than in C. suprapiscis, being as long as pereonite 2 and longer than propodus in the former (Templeton, 1836, fig. 6 a) and it is shorter than pereonite 2 and also shorter than the propodus in the later (Fig. 2 A, C)., Published as part of Galv��n-Villa, Cristian M. & Ay��n-Parente, Manuel, 2015, Caprella suprapiscis sp. nov. (Crustacea: Amphipoda: Caprellidae) from the Pacific coast of Mexico, pp. 569-578 in Zootaxa 3956 (4) on pages 570-577, DOI: 10.11646/zootaxa.3956.4.8, http://zenodo.org/record/243069, {"references":["Mori, A. & Yamato, S. (1993) Caprella simia Mayer, 1903 (Crustacea: Amphipoda) collected from the body surface of a frogfish Antennarius striatus (Shaw & Nodder, 1794). Nanki-Seibutu, 35, 41 - 46.","Hendrickx, M. E. & Ayon-Parente, M. (2014) Two new species of deep-water Caprella (Peracarida, Amphipoda, Caprellidae) from the Pacific coast of Mexico collected during the Talud XIV cruise, with a checklist of species of Caprellidae recorded for the Eastern Pacific. Crustaceana, 87, 41 - 63. http: // dx. doi. org / 10.1163 / 15685403 - 00003277","Takeuchi, I. & Oyamada, A. (2013) Description of two species of Caprella (Crustacea: Amphipoda: Caprellidae) from the North Pacific; C. californica Stimpson, 1857 and C. scauroides Mayer, 1903, with a new appraisal of species ranking for C. scauroides. Helgoland Marine Research, 67, 371 - 381. http: // dx. doi. org / 10.1007 / s 10152 - 012 - 0329 - 9"]}

Genus Areopaguristes Rahayu & McLaughlin, 2010 Stratiotes Thomson, 1899: 185 (junior homonym of Stratiotes Putzeys, 1846, Coleoptera).��� Rahayu, 2005: 4.���De Grave et al., 2009: 25. Areopaguristes Rahayu & McLaughlin, 2010: 67 (replacement name for preoccupied Stratiotes Thomson, 1899).���McLaughlin et al., 2010: 18. Emended diagnosis. Twelve pairs of bi- or quadriserial gills [no pleurobranch on fifth or eighth thoracic somites]. Shield with rostrum well developed or reduced. Ocular acicles simple, bi- or multidenticulate. Antennal peduncle with supernumerary segmentation. Maxillule with external lobe of endopod well developed, distinctly recurved. First maxilliped with epipod well developed or absent. Third maxilliped with coxal segments approximate or somewhat separated; crista dentata usually well developed, no accessory tooth; merus usually with 1 or more spines; carpus, propodus and dactyl usually unarmed. Chelipeds equal, subequal or unequal, often with left considerably larger, similar or dissimilar in armament; claws corneous, fingers opening in horizontal or oblique plane. Fourth pereopods subchelate or weakly semichelate, with or without preungual process developed at base of claw. Males with paired gonopores; first and second pleomeres each with pair of pleopods modified as gonopods; unpaired, unequally biramous left pleopods on pleomeres 3���4, pleopod 5 with external ramus well developed, internal ramus rudimentary. Females usually with paired gonopores; first pleomere with or without pair of modified pleopods (gonopods); pleomeres 2���4 with unequally biramous left pleopods; pleopod 5 as in male; brood pouch usually well developed, occasionally absent. Uropods asymmetrical. Telson with lateral indentations; posterior portion divided by median cleft into 2 subequal to markedly unequal lobes. Type species. Pagurus setosus Filhol, 1885. Remarks. With the addition of the two species discussed in this study, Aeropaguristes now contains 27 species worldwide (Tab. 1). Of these, nine occur in the Americas, with four in the eastern tropical Pacific: A. lemaitrei Ay��n-Parente & Hendrickx, 2012, A. mclaughlinae (Ay��n-Parente & Hendrickx, 2006), A. praedator (Glassell, 1937) nov. comb., and A. waldoschmitti Ay��n-Parente & Hendrickx, 2012; and five in the western Atlantic: A. hewatti (Wass, 1963), A. hummi (Wass, 1955), A. iris (Forest & de Saint Laurent, 1968), A. oxyophthalmus (Holthuis, 1959) nov. comb., and A. tudgei (Lemaitre & Felder, 2012). The remaining species occur in the Indowest Pacific. Species Geographical range Areopaguristes abbreviatus (Dechanc��, 1963) Madagascar Areopaguristes breviantennatus (Rahayu, 2005) Indonesia Areopaguristes cyanops (Forest, 1978) Nigeria, Cameroon Areopaguristes difficilis (Forest, 1952) Senegal Areopaguristes engyops (Barnard, 1947) South Africa Areopaguristes hewatti (Wass, 1963) Texas, USA Areopaguristes hispidus (A. Milne-Edwards & Bouvier, 1892) Liberia, Congo Areopaguristes hummi (Wass, 1955) North Carolina to Louisiana, Caribbean coast of Colombia Areopaguristes iris (Forest & de Saint Laurent, 1968) Brazil Areopaguristes japonicus (Miyake, 1961) Japan, Korea, China Areopaguristes lemaitrei Ay��n-Parente & Hendrickx, 2012 Mexican Pacific Areopaguristes mclaughlinae (Ay��n-Parente & Hendrickx, 2006) Mexican Pacific Areopaguristes micheleae (Rahayu, 2005) Indonesia Areopaguristes ngochoae (Rahayu, 2005) Indonesia Areopaguristes nigroapiculus (Komai, 2009) Japan, Far east Rusia Areopaguristes orbis (Komai, 2009) Izu Islands, Japan Areopaguristes oxyophthalmus (Holthuis, 1959) nov. comb. Gulf of Mexico, Caribbean in Puerto Rico and Colombia, Suriname, Brazil Areopaguristes perspicax (Nobili, 1906) Red Sea, Persian Gulf Areopaguristes pilosus (H. Milne Edwards, 1836) New Zealand Areopaguristes praedator (Glassell, 1937) nov. comb. Mexican Pacific to Costa Rica Areopaguristes rubrodiscus (Forest, 1952) Senegal Areopaguristes setosus (H. Milne Edwards, 1848) New Zealand Areopaguristes taenia (Komai, 1999) Ogosawara Islands, Ohsumi Islands Areopaguristes tuberculatus (Whitelegge, 1900) New SouthWales, Western Australia, Indonesia Areopaguristes tudgei Lemaitre & Felder, 2012 Belize Areopaguristes virilis (Forest, 1952) Guinea, Congo, Angola Areopaguristes waldoschmitti Ay��n-Parente & Hendrickx, 2012 Mexican Pacific, Published as part of Ay��n-Parente, Manuel, Hendrickx, Michel E. & Lemaitre, Rafael, 2015, Redescription and taxonomic status of Paguristes praedator Glassell, 1937 and P. oxyophthalmus Holthuis, 1959 (Anomura: Paguroidea: Diogenidae), with an emendation to the diagnosis of the genus Areopaguristes Rahayu & McLaughlin, 2010, pp. 491-509 in Zootaxa 3915 (4) on pages 492-493, DOI: 10.11646/zootaxa.3915.4.2, http://zenodo.org/record/234099, {"references":["Rahayu, D. L. (2005) Additions to the Indonesian fauna of the hermit crab genus Pseudopaguristes McLaughlin and a further division of the genus Paguristes Dana (Crustacea: Decapoda: Paguroidea: Diogenidae). Zootaxa, 831, 1 - 42.","Ayon-Parente, M. & Hendrickx, M. E. (2012) Two new species of hermit crabs of the genus Areopaguristes Rahayu & McLaughlin, 2010 (Crustacea: Anomura: Paguroidea: Diogenidae) from the eastern tropical Pacific. Zootaxa, 3407, 22 - 36.","Ayon-Parente, M. & Hendrickx, M. E. (2006) A new species of Stratiotes Thomson, 1899 (Anomura, Paguroidea, Diogenidae) from the eastern tropical Pacific. Zoosystema, 28 (2), 487 - 497.","Glassell, S. A. (1937) The Templeton Crocker Expedition. XI. Hermit crabs from the Gulf of California and the west coast of Lower California. Zoologica, 22, 241 - 263.","Holthuis, L. B. (1959) The Crustacea Decapoda of Suriname (Dutch Guiana). Zoologische Verhandelingen, 44, 1 - 296.","Lemaitre, R. & Felder, D. L. (2012) A new species of the hermit crab genus Areopaguristes Rahayu & McLaughlin, 2010 (Crustacea: Decapoda: Anomura: Diogenidae) discovered in the Mesoamerican Barrier Reef of Belize, Caribbean Sea.","Komai, T. (2009) A review of the northwestern Pacific species of the genus Paguristes (Decapoda: Anomura: Diogenidae). II. Species transferred to the genus Stratiotes, with descriptions of two new species. Natural History Research, 10 (2), 59 - 92."]}