Aegla buenoi n. sp. (Decapoda: Anomura): first record of aeglid crab from Cinzas River basin, Brazil Author Marçal, Ingrid Costa 0000-0001-7548-4925 Laboratório de Estudos de Invertebrados Aquáticos e Simbiontes (LabIAS), Departamento de Biologia Animal e Vegetal, Universidade Estadual de Londrina, 86057 - 970, Londrina, Paraná, Brazil. ingridmarcal@uel.br Author Páez, Fernanda Polli Laboratório de Estudos de Invertebrados Aquáticos e Simbiontes (LabIAS), Departamento de Biologia Animal e Vegetal, Universidade Estadual de Londrina, 86057 - 970, Londrina, Paraná, Brazil. Author Souza-Shibatta, Lenice Laboratório de Sistemática Molecular, Departamento de Biologia Animal e Vegetal, Universidade Estadual de Londrina, 86057 - 970, Londrina, Paraná, Brazil. Author Sofia, Silvia Helena Laboratório de Genética e Ecologia Animal (LAGEA), Departamento de Biologia Geral, Universidade Estadual de Londrina, 86057 - 970, Londrina, Paraná, B. Author Teixeira, Gustavo Monteiro Laboratório de Estudos de Invertebrados Aquáticos e Simbiontes (LabIAS), Departamento de Biologia Animal e Vegetal, Universidade Estadual de Londrina, 86057 - 970, Londrina, Paraná, Brazil. text Zootaxa 2021 2021-07-27 5005 3 291 303 journal article 10.11646/zootaxa.5005.3.4 1175-5326 5141770 A7FB5098-295C-496E-84FB-82CD3C524AB1 Aegla buenoi Marçal & Teixeira n. sp. ( Figs 3–5 ) urn:lsid:zoobank.org:act: F032E974-6EDE-4BA5-8577-17207631A62 Type-material. Holotype : male, Brazil , Paraná , Ibaiti , Paranapanema River basin, Cinzas River sub-basin, Carneiro stream, 23°57′19.71″S , 50°14′16.09″W , altitude 656 m , C.A. da Silva , R .H.C. do Nascimento and R . Rockembacher coll., 17.v.2016 ( MZUEL 249 ) . Paratypes : 1 male and 2 females , same data as holotype ( MZUEL 245 ) . 3 males and 2 females , Brazil , Paraná , Ibaiti , Paranapanema River basin, Cinzas River sub-basin, tributary of the Carneiro stream, 23°57′27.00″S , 50°14′5.00″W , altitude 620 m , G.M. Teixeira and J.J.S. Rosa coll., 12.vi.2017 ( MZUEL 246 , genetic vouchers: BOLD access AEGPR016-18 , AEGPR017-18 , AEGPR018-18 , AEGPR019-18 , AEGPR020-18 ) . Type-locality. Carneiro stream, city of Ibaiti, Paraná state , Brazil . Geographical distribution. The new species has been collected in two streams within the Cinzas River subbasin, Paranapanema River basin. Both streams are located in the city of Ibaiti, Paraná state , Brazil . FIGURE 3. Aegla buenoi n. sp. , male holotype (MZUEL 249). A, dorsal view of cephalothorax and anterior portion of abdomen. B, anterior portion of the cephalothorax showing the subrostral process (arrow). C, ventral view of ischium of major cheliped (left) showing five tubercles (arrow). D, third (thin arrow) and fourth (thick arrow) thoracic sternites. E, dorsal view of second abdominal epimeron (right side) showing anterolateral angle with corneous scale (thin arrow) and anterior margin almost straight (thick arrow). Bars: A = 5.0 mm, B−E = 1.0 mm. FIGURE 4. Aegla buenoi n. sp. , male holotype (MZUEL 249). A, lateral view of cephalothorax. B, anterior portion of the cephalothorax showing the subrostral process (thick white arrow), protogastric lobes pronounced (thin white arrow) and proeminences epigastric pronounced (black arrow). C, dorsal view of dactylus, propodus and carpus of major cheliped (left) showing palmar crest disciform (white arrow) and carpal ridge high (black arrow). D, ventral view of major cheliped (left) showing ischium with five tubercles (black arrows) and merus with two distal spines followed by three tubercles (white arrows). E, dorsal view of dactylus, propodus and carpus of minor cheliped (right) showing palmar crest disciform (white arrow) and carpal ridge high (black arrow). F, ventral view of minor cheliped (right) showing ischium with two tubercles (black arrows) and merus with one distal spine followed by five tubercles (white arrows). Bars = 1 mm. Diagnosis. Rostrum triangular, narrow base, reaching distal apex of compound eyes, carinate. Subrostral process well developed, occupying proximal half of subrostral margin, anterior and posterior margins forming obtuse angle (122°). Extra-orbital sinus deep. Anterolateral spines not reaching basal margin of cornea. Epigastric prominences pronounced and oval. Protogastric lobes pronounced. Cervical groove U-shaped. Cardiac area subrectangular. Proximal dorsal margin of dactylus with rudimentary or absent lobe. Palmar crest disciform, outer surface excavated. Subterminal lobe of carpus well defined, pointed. Ventromesial border of cheliped ischium with 4 or 5 tubercles. Anteromesial region of third thoracic sternite tapered. Anterior angle of second abdominal epimeron and ventral angles of third and fourth abdominal epimeron with corneous scale apically. Anterior margin of second abdominal epimeron almost straight. Uropods wide. Description of holotype . Carapace moderately convex, gastric region convex, dorsal surface scabrous, covered with punctations, anterior and posterior branchial areas expanded laterally (CW/CLE = 1.02) ( Figs 3A , 4A ). Rostrum triangular, narrow base (RBW/LMR = 0.98), reaching distal apex of compound eyes, carinate along entire length, small corneous scales on lateral margins, tip apparently broken; ventral portion of rostrum much higher than dorsal in profile. Rostral carina beginning at level of protogastric lobes, with row of corneous scales extending next to apex. Subrostral process well developed and covered by small setae, occupying proximal half of subrostral margin, tip rounded, anterior and posterior margins forming obtuse angle (122°) ( Figs 3B , 4B ). Eyestalk and cornea well developed. Orbital and extra-orbital sinuses deep. Orbital sinus U-shaped. Orbital spines well developed, with small terminal corneous scale. Anterolateral spines acuminate apically with small corneous scales terminally, not reaching basal margin of cornea. Epigastric prominences pronounced and oval, with corneous scales. Protogastric lobes pronounced, with corneous scales ( Fig. 4B ). Gastric area elevated in relation to hepatic lobes and rostrum in lateral view. Demarcation between hepatic lobes well defined. Lateral margins of hepatic lobes with small corneous scales. Cervical groove U-shaped. Transverse dorsal linea sinuous along its extension. Areola rectangular (AH/ [(APM+AAD)/2] = 2.54). Cardiac area subrectangular (TDL/PMC = 1.22). Epibranchial area strongly elongated, anterolateral angle with 2 corneous scales, lateral margin with row of small corneous scales and small setae. Lateral margins of anterior and posterior branchial areas with row of corneous scales and small setae. Chelipeds unequal, left largest. Major cheliped (left). Dactylus ( Fig. 4C ): dorsal margin and outer surface with small corneous scales, inner surface with setal tufts and scales; dorsal margin without proximal lobe; cutting margin with well-developed lobular basal tooth, followed by row of corneous scales up to distal end; row of small tufts of long setae next to cutting margin; pre-dactylar lobe well developed, rounded, smooth, without corneous scales. Propodus ( Fig. 4C ): outer surface granular, globose aspect; palmar crest disciform with outer surface excavated, margin poorly serrated, covered by corneous scales; fixed finger cutting margin with well-developed lobular basal tooth, followed by row of corneous scales up to distal end; inner and outer surfaces of fixed finger with rows of long setae tufts next to cutting margin. Carpus ( Fig. 4C ): dorsal margin with 2 proximal tubercles, 2 median spines, distal tubercle, double-tipped, each tubercle or spine with terminal corneous scale, subterminal lobe well defined, pointed, with small corneous scales, setae apically; inner surface with 2 distinct tubercles with acute corneous scale terminally; outer surface with carpal ridge high, with small corneous scales. Merus ( Fig. 4D ): dorsolateral edge with distal tubercle, with corneous scale terminally, followed by row of tubercles decreasing in size proximally; ventromesial edge with 2 distal spines, with corneous scale terminally, followed by 3 tubercles of similar size, with corneous scale; ventrolateral border with 2 distal tubercles, with terminal corneous scale, followed by several small tubercles proximally. Ischium ( Figs 3C , 4D ): dorsolateral edge with spine, with corneous scale terminally; ventromesial border with large proximal tubercle, 3 small median tubercles and large distal tubercle, each with terminal corneous scale; ventrolateral border smooth. Minor cheliped (right) similar to major cheliped except as noted hereafter. Dactylus ( Fig. 4E ): cutting margin with rudimentary lobular basal tooth. Propodus ( Fig. 4E ): cutting margin with rudimentary lobular basal tooth. Carpus ( Fig. 4E ): dorsal margin with 2 proximal tubercles, 2 median spines, distal spine, each with terminal corneous scale; inner surface with 5 tubercles, corneous scale terminally. Merus ( Fig. 4F ): ventromesial edge with distal spine, followed by 5 tubercles, each with terminal corneous scale. Ischium ( Fig. 4F ): ventromesial border with proximal tubercle, distal tubercle, each with terminal corneous scale. Second, third, and fourth pereiopods similar. Dactyli, propodi, carpi, meri and ischii with several rows of setal tufts and small scales on surface. Carpi and meri with row of tubercles with terminal corneous scale along dorsal margin. Meri and ischii with long setae concentrated along dorsal margin. Anteromesial region of third thoracic sternite tapered, projecting between coxae of third maxillipeds, with scattered setae. Fourth thoracic sternite with anterolateral angles produced anteriorly, with scattered setae ( Fig. 3D ). Anterolateral angle of second abdominal epimeron and ventral angles of third, fourth abdominal epimeron well defined, with corneous scale apically. Anterior margin of second abdominal epimeron almost straight ( Fig. 3E ). Uropods well developed, wide (WU/HWT = 1.04). Pleopods 2–5 absent. Telson divided by longitudinal suture. Anterolateral and posterolateral margins well differentiated. Variations. The rostrum is generally narrow base, but in some paratypes the base is wider than usual (RBW/ LMR = 1.03 ± 0.04; n = 5). In some specimens, the anterolateral spines can reach the basal margin of the cornea. The areola can be subrectangular (AH/[(APM+AAD)/2] = 2.12 ± 0.20; n = 4), trapezoidal (APM/AAD = 1.79 ± 0.10; n = 3), or rectangular (AH/[(APM+AAD)/2] = 2.31; n = 1). The cardiac area varies from subrectangular (TDL/PMC = 1.28 ± 0.06; n = 7) to trapezoidal (TDL/PMC = 1.45; n = 1). The proximal lobe on the dorsal margin of the dactylus of the major and minor chela may be rudimentary (as opposed to absent) ( Fig. 5A ). The palmar crest is rectangular instead of disciform in small individuals (CLE < 12 mm ) ( Figs 5B–C ). The ventromesial border of ischium may present four small tubercles instead of five ( Fig. 5D ). The anterolateral angle of second abdominal epimeron may be unarmed instead of present a corneous scale as in the holotype . The uropods are narrow (WU/HWT = 0.92 ± 0.03; n = 3) in some specimens. All measurements taken on type-series and morphometric relationships are summarized in Table 1 . Biology. Unknown. Etymology. The specific epithet is given in honor of Dr. Sérgio Luiz de Siqueira Bueno, for his outstanding contributions to the taxonomy and knowledge of the biology of aeglids. FIGURE 5. Aegla buenoi n. sp. , female paratype (MZUEL 245). A, dorsal view of the anterior region of the cephalothorax and chelipeds showing rudimentary lobe on dorsal margin of the dactylus (arrows). B, dorsal view of dactylus, propodus and carpus of major cheliped (left) showing palmar crest rectangular (arrow). C, dorsal view of dactylus, propodus and carpus of minor cheliped (right) showing palmar crest rectangular (arrow). D, ventral view of major cheliped (left) showing ischium with four tubercles (arrows). Bars = 1 mm. TABLE 1. Measurements (mm) and morphometric relationships of Aegla buenoi n. sp. AAD, areolar anterior demarcation; AH, areolar height; APM, areolar posterior margin; CL, carapace length including rostrum; CLE, carapace length excluding rostrum; CW, carapace width; F, female; H, holotype; HWT, half the maximum width of telson; LMR, lateral margin of rostrum; M, male; P1-P8, paratypes; PMC, mesial region of the posterior margin of the cephalothorax; RBW, rostral base width; TDL, transversal dorsal linea length; WU, width of uropod.

H	P1	P2	P3	P4	P5	P6	P7	P8
Sex	M	M	F	F	M	F	M	M	F
CL	29.20	31.30	14.10	21.50	10.30	10.60	12.80	13.70	11.60
CLE	24.80	26.60	11.80	17.90	8.60	9.00	10.80	11.90	9.90
CW	25.30	26.80	11.50	18.00	8.30	8.70	10.70	11.40	9.80
RBW	5.00	5.50	2.50	3.80	2.00	2.10	2.50	2.70	2.40
LMR	5.10	5.50	2.70	4.30	2.00	2.10	2.70	2.60	2.20
APM	3.90	5.80	2.20	3.80	1.70	1.60	2.40	2.40	1.70
AAD	2.80	3.30	1.50	2.00	1.00	1.00	1.50	1.50	1.20
AH	8.50	9.50	4.20	5.90	2.70	3.00	3.60	4.10	3.30
TDL	10.00	10.50	4.90	7.40	3.60	3.60	4.40	4.80	4.20
PMC	8.20	8.60	3.90	6.20	2.70	2.70	3.50	3.60	2.90
WU	4.70	5.00	2.20	3.40	1.60	1.60	1.80	2.20	1.80
HWT	4.50	4.80	2.30	3.80	1.60	1.50	2.00	2.00	1.80
CW/CLE	1.02	1.01	0.97	1.01	0.97	0.97	0.99	0.96	0.99
RBW/LMR	0.98	1.00	0.93	0.88	1.00	1.00	0.93	1.04	1.09
APM/AAD	1.39	1.76	1.47	1.90	1.70	1.60	1.60	1.60	1.42
AH/[(APM+ AAD)/2]	2.54	–	2.27	–	–	2.31	1.85	2.10	2.28
TDL/PMC	1.22	1.22	1.26	1.19	1.33	1.33	1.26	1.33	1.45
WU/HWT	1.04	1.04	0.96	0.89	1.00	1.07	0.90	1.10	1.00

TABLE 2. Genetic distances among Aegla species based on mitochondrial gene cytochrome c oxidase I (COI). Values are shown as percentages. Intraspecific distances are in bold.

Species	1	2	3	4	5	6	7	8
1. Aegla lata	0.0
2. Aegla jacutinga	3.3	0.1
3. Aegla buenoi n. sp.	3.5	2.1	0.0
4. Aegla castro	3.6	2.0	2.9	2.9
5. Aegla schmitti	5.4	3.7	4.1	4.2	2.7
6. Aegla odebrechtii	6.0	4.1	4.1	4.7	2.9	0.3
7. Aegla jarai	5.5	3.7	3.9	4.2	2.7	3.1	0.0
8. Aegla strinatii	6.8	5.2	4.8	5.4	3.8	4.0	3.8	0.1

Molecular data. Sequences of COI generated in this study were deposited in the BOLD database (access numbers AEGPR016-18, AEGPR017-18, AEGPR018-18, AEGPR019-18, AEGPR020-18).Altogether we analyzed 884 base pairs (bp) of COI with no insertions, deletions, or stop-codon. The mean base frequencies were: A = 0.2880, C = 0.1444, G = 0.1537, T = 0.4140. The genetic distance between A. buenoi n. sp. and its congeners ranged from 2.1% to 4.8% ( Table 2 ). Aegla jacutinga showed the lowest divergence relative to A . buenoi n. sp. , and the other species. In contrast, A . strinatii was found to be most distantly related to the new species and exhibited higher interspecific variations than the others, with a minimum K2P divergence of 3.8%. Most of the species showed intraspecific distances lower than 0.4%. Aegla castro and A. schmitti , however, presented intraspecific variations higher than 2.6% ( Table 2 ). Regarding species delimitation, the GMYC analysis indicated the presence of 10 independent strains ( Fig. 6 ). Two distinct clusters, with various well-supported subclusters, were obtained. Interestingly, the sequences of A. castro and A. schmitti formed non-monophyletic groups. On the other hand, all sequences of A. buenoi n. sp. were joined in the same cluster, indicating the presence of a single species.