Potamonautes kisangani, Cumberlidge & Johnson & Clark & Genner, 2021

Cumberlidge, Neil, Johnson, Emily, Clark, Paul F. & Genner, Martin J., 2021, Unravelling the Potamonautes lirrangensis (Rathbun, 1904) species complex (Potamoidea: Potamonautidae), with the description of two new species, European Journal of Taxonomy 744 (1), pp. 145-178 : 156-162

publication ID

https://doi.org/ 10.5852/ejt.2021.744.1309

publication LSID

lsid:zoobank.org:pub:F4DBFC27-1407-4926-BD0A-650C6C3854F4

DOI

https://doi.org/10.5281/zenodo.4694713

persistent identifier

https://treatment.plazi.org/id/77F6D732-392A-4B60-AA4A-AA2104D12C01

taxon LSID

lsid:zoobank.org:act:77F6D732-392A-4B60-AA4A-AA2104D12C01

treatment provided by

Plazi

scientific name

Potamonautes kisangani
status

sp. nov.

Potamonautes kisangani View in CoL sp. nov.

urn:lsid:zoobank.org:act:77F6D732-392A-4B60-AA4A-AA2104D12C01

Figs 1 View Fig , 4B View Fig , 5A View Fig , 6A–B View Fig , 7B View Fig , 8 View Fig , 11A View Fig , Table 1 View Table 1

Potamon (Potamonautes) lirrangensis – Rathbun 1921: 413–415, pls 25–26, figs 3, 8.

Diagnosis

Exorbital tooth large, spine-like; lateral margin of exorbital tooth lined by small teeth, angled outward at 45° to midline of carapace, straight, neither bulging outward (convex) nor curving inward (concave); epibranchial tooth small, granular, followed by large granules lining anterolateral margin ( Fig. 4B View Fig ); anterolateral margin posterior to epibranchial tooth curving strongly outward ( Fig. 4B View Fig ); postfrontal crest distinct, completely traversing carapace between epibranchial teeth; posterior surface of carapace with deep urogastric grooves ( Fig. 4B View Fig ). Male thoracic sternal sulcus S3/4 deep, distinct, V-shaped. Ischium of third maxilliped with thin but distinct vertical sulcus. Major chela with 3 large molars at proximal end of both fingers ( Fig. 6A–B View Fig ); major chela dactylus (moveable finger) and fixed finger (pollex of propodus) both elongated, straight, slender ( Fig. 6A–B View Fig ); cheliped carpus inner margin with 2 large, subequal, forward-pointing spines ( Fig. 7B View Fig ); cheliped merus inner lower margin with spine-like tooth distally. P5 carpus, propodus, and dactylus all shortened ( Fig. 8A–B View Fig ). G1 TA conspicuously widened by high, rounded dorsal lobe (as wide as TA width at TA-SA junction); G1 TA distal third straight, ending in pointed tip ( Fig. 11A View Fig ). G1 SA at junction with G1 TA with horizontal margin on ventral side, U-shaped indentation filled by conspicuous dorsal membrane on dorsal side.

Etymology

The new species is named for Kisangani, D.R. Congo, the locality where it was first collected. The specific epithet is used as a Latin noun in apposition. The vernacular name is the Kisangani freshwater crab.

Material examined

Holotype DEMOCRATIC REPUBLIC OF THE CONGO • ♂ adult (CW 60.5 mm); Kisangani , vicinity of Wagenia fishery ; 25 Apr. 1955; Smithsonian-Bredin Congo Exped., W.L. Schmitt leg.; USNM 98944 View Materials .

Paratypes DEMOCRATIC REPUBLIC OF THE CONGO • 2 ♂♂ (CW 59.5, 39.4 mm), 10 ♀♀ (CW 62.7, 61.1, 59.2, 56.9, 56.8, 56, 51.6, 48.3, 44.5, 40.3 mm), 3 ♀♀ ovig. (CW 66.5, 62.8, 54.7 mm); same collection data as for holotype; USNM 98944 View Materials .

Other material

DEMOCRATIC REPUBLIC OF THE CONGO • 1 ♂, 1 ♀, 1 ♀ ovig.; Kisangani ; Feb. 1915; A.M. Congo Exped., H. Lang leg.; USNM 54305 View Materials 3 ♀♀ (CW 59.8, 54.9, 45.1 mm), 1 ♀ ovig. (CW 54.8 mm); same collection data as for preceding; Apr. 1915; USNM 54306 View Materials 5 ♀♀ (CW 51.9, 49, 48.9, 45.6, 36.8 mm), 2 ♂♂ (CW 60.2, 29.2 mm); same collection data as for preceding; USNM 54307 View Materials 1 ♂ (CW 59.1 mm); Kisangani , vicinity of Wagenia fishery ; W.L. Schmitt Bredin Exped. leg.; USNM 98939 View Materials 3 ♀♀ (CW 40.4, 40, 24.8 mm); rocky gorge of Tshope Falls, Kisangani; 19 Apr. 1955; Smithsonian-Bredin Congo Exped., W.L. Schmitt leg.; USNM 98940 View Materials 1 ♀ (CW 53.6 mm), 3 juvs; Kisangani , vicinity of Wagenia fishery ; Smithsonian-Bredin Congo Exped., W.L. Schmitt leg.; USNM 98941 View Materials 2 ♀♀ ovig. (CW 56.5, 53.7 mm), 1 ♀ (CW 62.6 mm); Kisangani ; 20 Apr. 1955; Smithsonian-Bredin Congo Exped., W.L. Schmitt leg.; USNM 98942 View Materials 1 ♀ (with hatchlings, CW 60.1 mm); Kisangani ; 20 Apr. 1955; Smithsonian-Bredin Congo Exped., W.L. Schmitt leg.; USNM 98943 View Materials 1 ♂ (subadult CW 47.2 mm); Kisangani ; 22 Jun. 1955; G. Browne leg.; NHMUK 1955.6.22.65 1 ♂, 1 ♀; Kisangani ; Apr. 1915; A.M. Congo Exped., H. Lang leg.; MCZ CRU-10613 .

Description

See Diagnosis.

Size

Large-sized species, adult at CW 53 mm, largest known specimen CW 66 mm.

Colour

The colour of living specimens from Kisangani D.R. Congo was provided by Rathbun (1921: 415). The dorsal carapace is either dark blue, dark green, or dark brown, the thoracic sternum is pink with blue/ gray tones, and the pleon is yellow/white. The fixed and movable fingers of the chelae are dark brown/ black in recently preserved specimens ( Fig. 6A–B View Fig ), while the arthrodial membranes of the chelipeds are vermillion (vivid red/orange).

Distribution

This species is only known from the vicinity of Kisangani in the D.R. Congo ( Fig. 1 View Fig ).

Ecology

Kisangani lies in the Upper Congo Rapids Ecoregion (FEOW #539) ( Thieme et al. 2005; Abell et al. 2008). The field notes of Herbert Lang on the habitat of P. kisangani sp. nov. from Kisangani provided by Rathbun (1921: 415) indicate that although this species is found in large rivers, it favours shallow waters near river banks where drifting logs jam. At the Boyoma Falls near Kisangani these crabs were common above and below the cataracts, while in the Tshopo River crabs were abundant among the rocks and boulder fields above the Tshopo Falls, but were absent below the falls where the water was shallow and had a sandy substrate.

Remarks

This new species was recognized to accommodate a large number of specimens from Kisangani, D.R. Congo that were collected by two U.S. Expeditions: the American Museum Congo Expedition (1909–1915) led by Herbert O. Lang and James P. Chapin, and the Smithsonian-Bredin Expedition to the Belgian Congo, Sudan, Uganda, and Egypt (1955) led by Waldo L. Schmitt. The first U.S. expedition initially deposited a large number of specimens (in 10 samples) in the AMNH and subsequently gifted some of these (USNM 54305, 54306, 54307 and MCZ CRU-10613) to these other museums. All of the specimens from the first U.S. Congo expedition were attributed by Rathbun (1921) to P. lirrangensis s. lat., and she provided a description, photographs, and illustrations of this species ( Rathbun 1921: 413–415, pls 25–26, figs 3, 8). The second U.S. Congo expedition in 1955 also collected a number of specimens (in 7 samples) from Kisangani (examined in the present work) that were also initially attributed to P. lirrangensis s. lat. Figures of the carapace, chelipeds, and G1 of the adult male holotype from Kisangani, D.R. Congo ( Figs 4B View Fig , 5A View Fig , 6A–B View Fig , 7B View Fig , 8A–B View Fig , 11A View Fig ) are provided for comparison with

the other taxa included here. One character that distinguishes this species from P. lirrangensis s. str. is the epibranchial tooth, which is small and granular, followed by large granules lining the anterolateral margin in P. kisangani sp. nov. ( Fig. 4 B View Fig ) (vs pointed and as large as the other teeth lining the anterolateral margin in P. lirrangensis s. str. from Liranga; Fig. 4A View Fig ). The absence of DNA sequence data for any of the specimens from Kisangani means that it is not possible to test the monophyly of P. kisangani sp. nov. using molecular data.

Comparisons

The epibranchial tooth and anterolateral margin of P. kisangani sp. nov. from Kisangani ( Fig. 4B View Fig ) and of P. amosae sp. nov. from Lake Kivu ( Fig. 4C View Fig ) and the Malagarasi River ( Fig. 4D View Fig ; Reed & Cumberlidge 2006: pl. 5a) are similar in both species: the epibranchial tooth is a small granule that is followed by large granules lining the anterolateral margin. In contrast, the epibranchial tooth of P. lirrangensis s. str. from Liranga ( Fig. 4A View Fig ) and of P. orbitospinus from Lake Malawi ( Fig. 4E View Fig ) is pointed and as large as the other teeth lining the anterolateral margin.

The male thoracic sternal sulcus S3/4 of P. kisangani sp. nov. from Kisangani ( Fig. 8B View Fig ) and of P. orbitospinus from Lake Malawi ( Fig. 10B View Fig ) is deep, distinct, and V-shaped, whereas this sulcus is faint in P. amosae sp. nov. from Lake Kivu ( Fig. 9B View Fig ) and the Malagarasi River ( Reed & Cumberlidge 2006: pl. 5c).

The ischium of the third maxilliped of P. kisangani sp. nov. from Kisangani ( Fig. 5A View Fig ) and of P. orbitospinus from Lake Malawi ( Fig. 5C View Fig ) has a thin but distinct vertical sulcus, whereas this sulcus is faint and obscure in P. amosae sp. nov. from Lake Kivu ( Fig. 5B View Fig ) and the Malagarasi River ( Reed & Cumberlidge 2006: pl. 5c–d).

The chela dactylus (moveable finger) and fixed finger (pollex of propodus) of P. kisangani sp. nov. from Kisangani ( Fig. 6A–B View Fig ) are both elongated and slender, whereas the chela fingers in P. amosae sp. nov. from Lake Kivu ( Fig. 6C–D View Fig ) and from the Malagarasi River ( Fig. 6E–F View Fig ; Reed & Cumberlidge 2006: pl. 5a figs 46–47; NMU TRW1972.04), and in P. orbitospinus from Lake Malawi ( Fig. 6G–H View Fig ), are thick and broad.

The major chela has 3 large molars at the proximal ends of both fingers, with older specimens showing fusion of these teeth into a flat surface of the fixed finger in P. kisangani sp. nov. from Kisangani ( Figs 6A–B View Fig , 8A View Fig ) and in P. amosae sp. nov. from the Malagarasi River (CW 80.1 mm) ( Fig. 6E–F View Fig ; Reed & Cumberlidge 2006: pl. 5a figs 46–47), whereas the proximal parts of both fingers of the major chela in P. orbitospinus from Lake Malawi ( Fig. 6G–H View Fig ) has enlarged, rounded, separate (unfused) teeth.

The P5 carpus, propodus, and dactylus of P. orbitospinus from Lake Malawi ( Figs 10B View Fig , 13 View Fig ) are all elongated and slender, whereas these ambulatory leg articles in P. kisangani sp. nov. from Kisangani ( Fig. 8A–B View Fig ) and of P. amosae sp. nov. from Lake Kivu ( Fig. 9A–B View Fig ) and the Malagarasi River ( Reed & Cumberlidge 2006: pl. 5a) are all short and stocky.

The G1 TA in P. kisangani sp. nov. from Kisangani ( Fig. 11A View Fig ) and P. amosae sp. nov. from Lake Kivu ( Fig. 11B–D, F View Fig ) and the Malagarasi River ( Reed & Cumberlidge 2006: pl. 5c–d fig. 152) is only slightly widened by a low dorsal lobe and the TA ends in either a straight, or only slightly upcurved tip. This contrasts with the G1 TA in P. orbitospinus from Lake Malawi, which is conspicuously widened by a high, rounded dorsal lobe (as wide as the TA width at the TA-SA junction) and the G1 TA ends in a strongly curved upwards tip ( Fig. 12A–H View Fig ).

Kingdom

Animalia

Phylum

Arthropoda

Class

Malacostraca

Order

Decapoda

Family

Potamonautidae

Genus

Potamonautes

Loc

Potamonautes kisangani

Cumberlidge, Neil, Johnson, Emily, Clark, Paul F. & Genner, Martin J. 2021
2021
Loc

Potamon (Potamonautes) lirrangensis

Rathbun M. J. 1921: 413
1921
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