List of saltwater species that form a part of the crustacean fauna of South Africa
Map of the Southern African coastline showing some of the landmarks referred to in species range statements Thelist of marine crustaceans ofSouth Africa is a list ofsaltwater species that form a part of the crustacean (PhylumArthropoda , several classes)fauna of South Africa . This list does not include the freshwater and terrestrial crustaceans. The list follows theSANBI listing oniNaturalist , and does not always agree withWoRMS for distribution.
Crustaceans Latin word "crustacea" meaning: "those with shells" or "crusted ones") areinvertebrate animals that constitute one group ofarthropods that are traditionally a part of thesubphylum Crustacea (/k r ə ˈ s t eɪ ʃ ə aquatic arthropods including the more familiardecapods (shrimps ,prawns ,crabs ,lobsters andcrayfish ),seed shrimps ,branchiopods ,fish lice ,krill ,remipedes ,isopods ,barnacles ,copepods ,opossum shrimps ,amphipods andmantis shrimp . The crustacean group can be treated as a subphylum under theclade Mandibulata . It is now well accepted that thehexapods (insects andentognathans ) emerged deep in the crustacean group, with the completed pan-group referred to asPancrustacea . The three classesCephalocarida ,Branchiopoda andRemipedia are more closely related to the hexapods than they are to any of the other crustaceans (oligostracans andmulticrustaceans ).
The 67,000 described species range in size fromStygotantulus stocki Japanese spider crab with a leg span of up to 3.8 m (12.5 ft) and a mass of 20 kg (44 lb). Like otherarthropods , crustaceans have anexoskeleton , which theymoult to grow. They are distinguished from other groups of arthropods, such asinsects ,myriapods andchelicerates , by the possession ofbiramous (two-parted) limbs, and by theirlarval forms , such as thenauplius stage ofbranchiopods andcopepods .
Most crustaceans are free-livingaquatic animals , but some areterrestrial (e.g.woodlice ,sandhoppers ), some areparasitic (e.g.Rhizocephala ,fish lice ,tongue worms ) and some aresessile (e.g.barnacles ). The group has an extensivefossil record , reaching back to theCambrian . More than 7.9 million tons of crustaceans per year are harvested by fishery or farming for human consumption, consisting mostly ofshrimp and prawns .Krill andcopepods are not as widely fished, but may be the animals with the greatestbiomass on the planet, and form a vital part of the food chain. The scientific study of crustaceans is known ascarcinology (alternatively,malacostracology ,crustaceology orcrustalogy ), and a scientist who works in carcinology is acarcinologist . (Full article...
[ edit ] [ edit ] [ edit ] [ edit ] [ edit ] [ edit ] Family Centropagidae [ edit ] Family Clausocalanidae [ edit ] Family Metridinidae [ edit ] Family Paracalanidae [ edit ] Family Rhincalanidae [ edit ] Family Subeucalanidae [ edit ] [ edit ] Family Ectinosomatidae [ edit ] Family Porcellidiidae [ edit ] [ edit ] [ edit ] Family Sapphirinidae [ edit ] [ edit ] [ edit ] Family Poecilasmatidae [ edit ] Order Scalpelliformes [ edit ] Family Calanticidae [ edit ] [ edit ] Arcoscalpellum botellinae Arcoscalpellum michelottianum Seguenza , 1876)Catherinum sinuatum Pilsbryiscalpellum capense Pilsbryiscalpellum subalatum Tarasovium brevicaulus Tarasovium eumitos Tarasovium natalense Tarasovium valvulifer Vertebroscalpellum micrum Verum agulhense Verum branchiumcancri Verum cancellatum Verum carinatum Verum porcellanum Subfamily Meroscalpellinae [ edit ] Subfamily Scalpellinae [ edit ] [ edit ] [ edit ] Subfamily Archaeobalaninae [ edit ] [ edit ] Subfamily Megabalaninae [ edit ] [ edit ] [ edit ] Subfamily Notochthamalinae [ edit ] [ edit ] Family Coronulidae Subfamily Coronulinae [ edit ] [ edit ] [ edit ] [ edit ] [ edit ] [ edit ] [ edit ] [ edit ] [ edit ] [ edit ] [ edit ] [ edit ] [ edit ] [ edit ] [ edit ] [ edit ] [ edit ] [ edit ] [ edit ] [ edit ] [ edit ] [ edit ] [ edit ] [ edit ] [ edit ] [ edit ] [ edit ] [ edit ] [ edit ] [ edit ] [ edit ] [ edit ] [ edit ] [ edit ] [ edit ] [ edit ] [ edit ] [ edit ] [ edit ] [ edit ] [ edit ] [ edit ] [ edit ] [ edit ] [ edit ] [ edit ] [ edit ] [ edit ] [ edit ] [ edit ] [ edit ] [ edit ] Ampelisca acris [ 4] Ampelisca anisuropa [ 4] Ampelisca anomala [ 4] Ampelisca brachyceras [ 4] Ampelisca brevicornis [ 4] Ampelisca chiltoni [ 4] Ampelisca diadema [ 4] Ampelisca excavata [ 4] Ampelisca fusca [ 4] Ampelisca insignis [ 4] Ampelisca miops [ 4] Ampelisca natalensis [ 4] Ampelisca palmata [ 2] [ 4] Ampelisca spinimana [ 4] Byblis gaimardii [ 4] [ edit ] [ edit ] [ edit ] [ edit ] [ edit ] [ edit ] [ edit ] [ edit ] [ edit ] [ edit ] [ edit ] Caprella circur Caprella danilevski Caprella equilibra [ 2] Caprella laevipes Caprella natalensis Caprella penantis Caprella scaura Caprella triodos Eupariambus fallax Hemiaegina minuta Metaprotella haswelliana Metaprotella macrodactylos Monoliropus falcimanus Orthoprotella mayeri Paracaprella pusilla Paracaprella tenuis Paradeutella serrata Pseudaeginella tristanensis Pseudoprotella phasma [ edit ] [ edit ] [ edit ] [ edit ] [ edit ] Isaeopsis tenax Ischyrocerus anguipes Ischyrocerus carinatus Ischyrocerus ctenophorus Ischyrocerus gorgoniae Jassa falcata Jassa marmorata Jassa morinoi Jassa slatteryi Parajassa chikoa Ventojassa frequens [ edit ] [ edit ] [ edit ] [ edit ] Gammaropsis chelifera [ 4] Gammaropsis holmesi [ 4] Gammaropsis longicarpa [ 4] Gammaropsis palmoides [ 4] Gammaropsis pseudodenticulata [ 7] Gammaropsis scissimana [ 4] Gammaropsis sophiae [ 4] Latigammaropsis afra [ 4] Latigammaropsis atlantica [ 4] Photis dolichommata [ 4] Photis kapapa [ 4] Photis longidactyla [ 4] Photis longimana [ 4] Photis uncinata [ 4] [ edit ] [ edit ] Aora anomala [ 4] Aora gibbula [ 4] Aora inflata [ 8] Aora kergueleni [ 2] [ 4] Autonoe hirsutipes [ 4] Bemlos teleporus [ 9] Camacho bathyplous [ 4] Grandidierella bonnieroides [ 4] Grandidierella chelata [ 4] Grandidierella lignorum [ 4] Grandidierella lutosa [ 4] Grandidierella nyala [ 10] Lemboides acanthiger [ 4] Lemboides afer [ 4] Lembos hypacanthus [ 4] Microdeutopus thumbellinus [ 4] Xenocheira leptocheira [ edit ] [ edit ] [ edit ] [ edit ] Ampithoe africana [ 4] Amphithoe falsa [ 4] Ampithoe kava Ampithoe ramondi [ 4] Cymadusa cavimana Cymadusa filosa [ 2] [ 4] Exampithoe (Exampithoe) natalensis [ 4] Macropisthopus stebbingi [ 4] Paragrubia vorax [ 4] Peramphithoe humeralis [ edit ] [ edit ] [ edit ] [ edit ] Aquadulcaris andronyx Aquadulcaris auricularius Aquadulcaris crassicornis Aquadulcaris dentata Aquadulcaris marunuguis Aquadulcaris pheronyx Mathamelita aequidentata Paramelita aurantius Paramelita barnardi Paramelita capensis Paramelita flexa Paramelita granulicornis Paramelita kogelensis Paramelita magna Paramelita magnicornis Paramelita nigroculus Paramelita odontophora Paramelita parva Paramelita pillicornis Paramelita pinnicornis Paramelita platypus Paramelita seticornis Paramelita spinicornis Paramelita triangula Paramelita tulbaghensis Paramelita validicornis [ edit ] [ edit ] [ edit ] [ edit ] [ edit ] [ edit ] [ edit ] [ edit ] [ edit ] Austromaera bruzelii [ 14] Austromaera mastersii [ 4] [ 15] Ceradocus natalensis [ 4] Ceradocus (Denticeradocus) rubromaculatus [ 2] [ 4] Elasmopoides chevreuxi [ 4] Elasmopus alalo [ 4] Elasmopus japonicus [ 4] Elasmopus pectenicrus [ 4] Elasmopus rapax [ 4] Hamimaera hamigera [ 4] Jerbarnia mecochira [ 4] Linguimaera boecki [ 4] Maera grossimana [ 4] Maera hirondellei [ 4] Maera inaequipes [ 4] Maera vagans [ 4] Mallacoota subcarinata [ 4] Othomaera komma [ 4] [ 16] Othomaera lobata [ 17] Othomaera thrixa [ 4] Parelasmopus suluensis [ 4] Quadrimaera pacifica Quadrimaera serrata [ 4] [ 18] Quadrivisio aviceps [ 4] Zygomaera emarginata [ 4] [ edit ] [ edit ] [ edit ] [ edit ] [ edit ] [ edit ] [ edit ] [ edit ] [ edit ] Africorchestia quadrispinosa [ 2] Cochinorchestia notabilis Eorchestia rectipalma Floresorchestia anomala Floresorchestia ancheidos Orchestia dassenensis Orchestia gammarellus Platorchestia platensis Talitriator africana Talitriator calva Talitriator cylindripes Talitriator eastwoodae Talitriator setosa Talitroides alluaudi Talitroides topitotum Talorchestia australis Talorchestia capensis [ 2] [ edit ] [ edit ] [ edit ] Family Gynodiastylidae [ edit ] Dic calmani [ 20] Dic formosae [ 20] Dic platytelson [ 20] Diastylis algoae [ 20] Diastylis namibiae [ 20] Diastylis hexaceros [ 20] Leptostylis attenuatus [ 20] Leptostylis gilli [ 20] Leptostylis faurei [ 20] Leptostylis macruroides [ 20] Makrokylindrus (Adiastylis) acanthodes [ 20] Makrokylindrus (Adiastylis) aculeatus [ 20] Makrokylindrus (Adiastylis) bicornis [ 20] Makrokylindrus (Adiastylis) spinifer [ 20] Makrokylindrus (Makrokylindrus) deinotelson [ 20] Makrokylindrus (Makrokylindrus) fragilis [ 20] Makrokylindrus (Makrokylindrus) mundus [ 20] Vemakylindrus stebbingi [ 20] [ edit ] [ edit ] [ edit ] Bentheogennema intermedia [ 21] Gennadas bouvieri Gennadas brevirostris [ 21] Gennadas capensis [ 21] Gennadas clavicarpus [ 21] Gennadas elegans [ 21] Gennadas gilchristi [ 21] Gennadas kempi [ 21] Gennadas incertus [ 21] Gennadas parvus [ 21] Gennadas scutatus [ 21] Gennadas talismani [ 21] Gennadas tinayrei [ 21] Gennadas valens [ 21] [ edit ] [ edit ] Funchalia woodwardi [ 21] Macropetasma africana [ 21] Metapenaeus monoceros [ 21] Metapenaeus stebbingi Metapenaeopsis andamanensis [ 21] Metapenaeopsis mogiensis [ 21] Metapenaeopsis philippii [ 21] Metapenaeopsis quinquedentata [ 21] Parapenaeopsis acclivirostris [ 21] Parapenaeus fissurus [ 21] Parapenaeus investigatoris [ 21] Penaeopsis rectacuta [ 21] Penaeus canaliculatus [ 21] Penaeus indicus [ 21] Penaeus japonicus [ 21] Penaeus latisulcatus [ 21] Penaeus monodon [ 21] Penaeus semisulcatus [ 21] [ edit ] [ edit ] Acetes erythraeus [ 21] Acetes natalensis [ 21] Allosergestes pectinatus [ 21] Allosergestes sargassi [ 21] Deosergestes corniculum [ 21] Deosergestes disjunctus [ 21] Eusergestes arcticus [ 22] [ 1] Neosergestes orientalis [ 21] Parasergestes armatus [ 21] Petalidium foliaceum [ 21] Sergestes atlanticus [ 21] Sergia grandis [ 21] Sergia laminata [ 21] Sergia potens [ 21] Sergia prehensilis [ 21] Sergia regalis [ 21] Sergia scintillans [ 21] Sergia talismani [ 21] [ edit ] [ edit ] [ edit ] [ edit ] [ edit ] [ edit ] [ edit ] [ edit ] [ edit ] [ edit ] Aniculus aniculus [ 2] Calcinus laevimanus [ 2] Clibanarius longitarsus [ 2] Clibanarius virescens [ 2] Dardanus arrosor [ 2] Dardanus megistos [ 2] Dardanus pedunculatus [ 2] Diogenes brevirostris [ 2] Diogenes costatus [ 2] Diogenes extricatus [ 2] Diogenes senex [ 2] Paguristes gamianus [ 5] [ edit ] [ edit ] [ edit ] [ edit ] [ edit ] [ edit ] [ edit ] [ edit ] [ edit ] [ edit ] [ edit ] [ edit ] [ edit ] [ edit ] [ edit ] [ edit ] [ edit ] [ edit ] [ edit ] [ edit ] [ edit ] checked to here
[ edit ] [ edit ] [ edit ] Subfamily Xanthinae [ edit ] Subfamily Zosiminae [ edit ] [ edit ] [ edit ] [ edit ] Subfamily Varuninae [ edit ] [ edit ] Family Macrophthalmidae [ edit ] [ edit ] [ edit ] Parvorder Podotremata [ edit ] [ edit ] [ edit ] [ edit ] Potamonautes anchietae Potamonautes bayonianus Potamonautes brincki Potamonautes calcaratus Potamonautes clarus Potamonautes dentatus Potamonautes depressus Potamonautes dubius Potamonautes granularis Potamonautes kensleyi Potamonautes lividus Potamonautes macrobrachii Potamonautes mutandensis Potamonautes obesus Potamonautes parvicorpus Potamonautes parvispina Potamonautes perlatus Potamonautes sidneyi Potamonautes unispinus Potamonautes warreni [ edit ] Alpheus architectus [ 21] Alpheus bidens [ 21] Alpheus bisincisus [ 21] Alpheus collumianus [ 21] Alpheus deuteropus [ 21] Alpheus diadema [ 21] Alpheus edwardsii [ 21] Alpheus frontalis [ 21] Alpheus gracilipes [ 21] Alpheus lobidens [ 21] Alpheus hippothoe [ 21] Alpheus longecarinatus [ 21] Alpheus lottini [ 21] Alpheus malabaricus [ 21] Alpheus nonalter [ 21] Alpheus notabilis [ 21] Alpheus obesomanus [ 21] Alpheus parvirostris [ 21] Alpheus rapacida [ 21] Alpheus rapax [ 21] Alpheus strenuus strenuus [ 21] Alpheus sulcatus [ 21] Alpheus villosus [ 21] Alpheus waltervadi [ 21] Athanas djiboutensis [ 21] Athanas minikoensis [ 21] Athanas nitescens [ 21] Arete indicus [ 21] Betaeus jucundus [ 21] Racilius compressus [ 21] Salmoneus rostratus [ 21] Synalpheus charon [ 21] Synalpheus digueti [ 21] Synalpheus jedanensis [ 21] Synalpheus tumidomanus tumidomanus [ 21] Family Hippolytidae [ edit ] Alope orientalis [ 21] Eualus cteniferus [ 21] Eualus makrognathus [ 21] Eualus pax [ 21] Exhippolysmata tugelae [ 21] Gelastocaris paronae [ 21] Hippolyte catagrapha [ 21] Hippolyte kraussiana [ 21] Hippolyte palliola [ 21] Hippolyte ventricosa [ 21] Latreutes mucronatus [ 21] Latreutes pymoeus [ 21] Lebbeus saldanhae [ 21] Leontocaris paulsoni [ 21] Lysmata amboinensis [ 2] Lysmata debelius [ 2] Lysmata kuekenthali [ 21] Lysmata vittata [ 21] Merhippolyte agulhasensis [ 21] Merhippolyte calmani [ 21] Saron marmoratus [ 21] Thor amboinensis [ 21] Tozeuma armatum [ 21] [ edit ] [ edit ] Aegaeon cataphractus [ 21] Aegaeon lacazei [ 21] Crangon capensis [ 21] Metacrangon bellmarleyi [ 21] Parapontophilus gracilis gracilis [ 21] Parapontophilus occidentalis [ 21] Philocheras pilosus [ 21] Philocheras sculptus [ 21] Philocheras megalocheir [ 21] Philocheras hendersoni [ 21] Family Glyphocrangonidae [ edit ] [ edit ] [ edit ] Acanthephyra acanthitelsonis [ 21] Acanthephyra brevirostris [ 21] Acanthephyra corallina [ 21] Acanthephyra eximia [ 21] Acanthephyra pelagica [ 21] Acanthephyra quadrispinosa [ 21] Acanthephyra stylorostratis [ 21] Acanthephyra tenuipes [ 21] Notostomus elegans [ 21] Meningodora mollis [ 21] Hymenodora gracilis [ 21] Family Oplophoridae [ edit ] [ edit ] Family Gnathophyllidae [ edit ] [ edit ] Leander tenuicornis [ 21] Macrobrachium equidens [ 21] Macrobrachium idea [ 21] Macrobrachium lepidactylus [ 21] Macrobrachium petersii [ 21] Macrobrachium rude [ 21] Macrobrachium scabriculum [ 21] Macrobrachium vollenhoveni [ 21] Nematopalaemon tenuipes [ 21] Palaemon capensis [ 21] Palaemon concinnus [ 21] Palaemon debilis [ 21] Palaemon elegans [ 21] Palaemon maculatus [ 21] Palaemon pacificus [ 21] Palaemon peringueyi [ 2] Subfamily Pontoniinae [ edit ] Anchistus custos [ 21] Ancylomenes aesopius Ancylomenes luteomaculatus Conchodytes tridacnae [ 21] Coralliocaris graminea [ 21] Cuapetes demani [ 21] Cuapetes grandis [ 21] Cuapetes seychellensis [ 21] Harpiliopsis beaupresii [ 21] Harpiliopsis depressa [ 21] Ischnopontonia lophos [ 21] Jocaste lucina [ 21] Lipkemenes lanipes [ 21] Palaemonella rotumana [ 21] Periclimenaeus natalensis [ 21] Periclimenaeus tridentatus [ 21] Periclimenaeus uropodialis [ 21] Periclimenes brevicarpalis [ 21] Periclimenes commensalis [ 21] Periclimenes delagoae [ 21] Periclimenes imperator [ 21] Platycaris latirostris [ 21] [ edit ] Chlorotocus crassicornis [ 21] Heterocarpus dorsalis [ 21] Heterocarpus laevigatus [ 21] Heterocarpus tricarinatus [ 21] Heterocarpus woodmasoni [ 21] Pandalina brevirostris [ 21] Plesionika acanthonotus [ 21] Plesionika edwardsii [ 21] Plesionika martia [ 21] Stylopandalus richardi [ 21] Superfamily Pasiphaeoidea family Pasiphaeidae [ edit ] [ edit ] [ edit ] Infraorder Gebiidea [ edit ] Infraorder Stenopodidea [ edit ] Family Stenopodidae [ edit ] Family Euphausiidae [ edit ] [ edit ] Family Antarcturidae [ edit ] Astacilla brevipes [ 26] Astacilla corniger [ 26] Astacilla lobulata [ 26] Astacilla longipes [ 26] Astacilla longispina [ 26] Astacilla mediterranea Astacilla pustulata [ 26] Astacilla tranquilla [ 26] Arcturina hexagonalis [ 26] Arcturina scutula [ 26] Arcturina triangularis [ 26] Arcturinoides sexpes [ 26] Idarcturus platysoma [ 26] Microarcturus oudops [ 26] Microarcturus similis [ 26] Neastacilla bacillus [ 26] Family Holidoteidae [ edit ] Family Holognathidae [ edit ] Engidotea lobata [ 26] Euidotea peronii [ 26] Glyptidotea lichtensteini [ 26] Idotea indica [ 26] Idotea metallica [ 26] Idotea ziczac [ 26] Paridotea apposita [ 26] Paridotea fucicola [ 26] Paridotea reticulata [ 26] Paridotea rubra [ 26] Paridotea ungulata [ 26] Synidotea hirtipes [ 26] Synidotea setifer [ 26] Synidotea variegata [ 26] Suborder Cymothoida [ edit ] [ edit ] Amakusanthura africana [ 26] Apanthura sandalensis [ 26] Cyathura estuaria [ 26] Haliophasma austroafricanum [ 26] Haliophasma coronicauda [ 26] Haliophasma foveolata [ 26] Haliophasma hermani [ 26] Haliophasma macrurum [ 26] Haliophasma pseudocarinata [ 26] Haliophasma tricarinata [ 26] Malacanthura linguicauda [ 26] Malacanthura ornata [ 26] Mesanthura catenula [ 26] Notanthura caeca [ 26] Quantanthura serenasinus [ 26] Quantanthura remipes [ 26] Family Expanathuridae [ edit ] Family Leptanthuridae [ edit ] Family Paranthuridae [ edit ] [ edit ] Aega monophthalma [ 26] Aega monilis [ 26] Aega semicarinata [ 26] Aega webbii [ 26] Aegapheles antillensis [ 26] Aegiochus gracilipes [ 26] Rocinela dumerilii [ 26] Rocinela granulosa [ 26] Rocinela orientalis [ 26] Syscenus infelix [ 26] Cirolana fluviatilis Cirolana imposita [ 26] Cirolana incisicauda [ 26] Cirolana littoralis [ 26] Cirolana luciae [ 26] Cirolana meinerti [ 26] Cirolana palifrons [ 26] Cirolana parva [ 26] Cirolana rugicauda [ 26] Cirolana saldanha [ 26] Cirolana sulcata [ 26] Cirolana theleceps [ 26] Cirolana transcostata [ 26] Cirolana undulata [ 26] Cirolana venusticauda [ 26] Conilorpheus [ 26] Conilorpheus scutifrons [ 26] Eurydice barnardi Eurydice kensleyi Eurydice longicornis [ 26] Excirolana latipes [ 26] Excirolana natalensis [ 26] Gnatholana mandibularis [ 26] Metacirolana bicornis [ 26] Natatolana borealis [ 26] Natatolana hirtipes [ 26] Natatolana natalensis [ 26] Natatolana pilula [ 26] Natatolana virilis [ 26] Parabathynomus natalensis [ 26] Politolana obtusispina [ 26] family Corallanidae [ edit ] Anilocra capensis [ 26] Anilocra leptosoma Cinusa tetrodontis [ 26] Ceratothoa imbricata [ 26] Cymothoa borbonica [ 26] Elthusa raynaudii [ 26] Mothocya melanosticta [ 26] Nerocila orbignyi [ 26] Nerocila phaiopleura [ 26] Nerocila serra [ 26] Nerocila trichiura [ 26] Suborder Limnoriidea [ edit ] [ edit ] Suborder Sphaeromatidea [ edit ] [ edit ] [ edit ] Family Sphaeromatidae [ edit ] Artopoles capensis [ 26] Artopoles natalis [ 26] Cassidias africana [ 26] Cassidinidea monodi [ 26] Cilicaea latreillei [ 26] Cymodoce acanthiger [ 26] Cymodoce africana [ 26] Cymodoce alia [ 26] Cymodoce alis [ 26] Cymodoce amplifrons [ 26] Cymodoce cavicola [ 26] Cymodoce comans [ 26] Cymodoce cryptodoma [ 26] Cymodoce excavans [ 26] Cymodoce falcata [ 26] Cymodoce lis [ 26] Cymodoce natalensis [ 26] Cymodoce radiata [ 26] Cymodoce setulosa [ 26] Cymodoce tetrahele [ 26] Cymodoce tuberculata [ 26] Cymodoce umbonata [ 26] Cymodoce uncinata [ 26] Cymodoce unguiculata [ 26] Cymodoce valida [ 26] Cymodoce velutina [ 26] Cymodoce zanzibarensis [ 26] Cymodocella cancellata [ 26] Cymodocella diateichos [ 26] Cymodocella eutylos [ 26] Cymodocella magna [ 26] Cymodocella pustulata [ 26] Cymodocella sublevis [ 26] Dynamenella dioxus [ 26] Dynamenella huttoni [ 2] Dynamenella navicula [ 26] Dynamenella taurus [ 26] Dynoides serratisinus [ 26] Exosphaeroma antikraussi [ 26] Exosphaeroma brevitelson [ 26] Exosphaeroma estuarium [ 26] Exosphaeroma hylecoetes [ 26] Exosphaeroma kraussi [ 26] Exosphaeroma laeviusculum [ 26] Exosphaeroma pallidum [ 26] Exosphaeroma planum [ 26] Exosphaeroma porrectum [ 26] Exosphaeroma truncatitelson [ 26] Exosphaeroma varicolor [ 26] Ischyromene australis [ 26] Ischyromene bicolor [ 26] Ischyromene macrocephala [ 26] Ischyromene ovalis [ 26] Ischyromene scabricula [ 26] Isocladus mimetes [ 26] Isocladus otion [ 26] Isocladus tristense [ 26] Paracilicaea clavus [ 26] Paracilicaea mossambica [ 26] Paracilicaea teretron [ 26] Parasphaeroma prominens [ 26] Parisocladus perforatus [ 26] Parisocladus stimpsoni [ 26] Pseudosphaeroma barnardi [ 26] Sphaeramene microtylotos [ 26] Sphaeramene polytylotos [ 26] Sphaeroma annandalei [ 26] Sphaeroma serratum [ 26] Sphaeroma terebrans [ 26] Sphaeroma walkeri [ 26] Stathmos coronatus [ 26] Zuzara furcifer [ 26] [ edit ] Family Haploniscidae [ edit ] Family Ischnomesidae [ edit ] [ edit ] Subfamily Eurycopinae [ edit ] Subfamily Ilyarachninae [ edit ] Subfamily Syneurycopinae [ edit ] Family Joeropsididae [ edit ] Family Macrostylidae [ edit ] [ edit ] Family Paramunnidae [ edit ] Superfamily Janiroidea incertae sedis [ edit ] [ edit ] Family Stenetriidae [ edit ] [ edit ] [ edit ] Subfamily Athelginae [ edit ] Subfamily Bopyrinae [ edit ] Subfamily Hemiarthrinae [ edit ] Subfamily Keponinae [ edit ] Subfamily Orbioninae [ edit ] Subfamily Pseudioninae [ edit ] [ edit ] Family Cyproniscidae [ edit ] Family Alloniscidae [ edit ] [ edit ] [ edit ] [ edit ] Subclass Phyllocarida [ edit ] [ edit ] Subclass Hoplocarida [ edit ] [ edit ] Superfamily Gonodactyloidea. family Gonodactylidae [ edit ] Family Odontodactylidae [ edit ] [ edit ] [ edit ]
^a b c d e f g h i j k l m n o p q r s t u v w x y z aa ab ac ad ae af ag ah ai aj ak al am an ao ap aq ar as Gibbons, Mark J. (1999).An introduction to the Zooplankton of the Benguela Current Region .ISBN 0-620-24225-6 ^a b c d e f g h i j k l m n o p q r s t u v w x y z aa ab ac ad ae af ag ah ai aj ak al am an ao ap aq ar as at au av aw ax ay az ba bb bc bd be bf bg bh bi bj bk bl bm bn bo bp bq br bs bt bu bv bw bx by bz ca cb cc cd ce cf cg ch ci cj ck cl cm cn co cp cq cr cs ct cu cv cw cx cy cz da db dc dd de df dg dh di dj dk dl dm dn do dp dq dr ds dt du dv dw dx dy dz ea eb ec ed ee ef eg eh ei ej ek el em en eo ep eq er es et eu ev ew ex ey ez fa fb fc fd fe ff fg fh fi fj fk fl fm fn fo fp fq fr fs ft fu Branch, G.M.; Branch, M.L.; Griffiths, C.L.; Beckley, L.E. (2010).Two Oceans: a guide to the marine life of southern Africa (2nd ed.). Cape Town: Struik Nature.ISBN 978-1-77007-772-0 ^ Walter, T.C. & Boxshall, G. (2019). World of Copepods database. Subeucalanus mucronatus (Giesbrecht, 1888). Accessed through: World Register of Marine Species at:http://www.marinespecies.org/aphia.php?p=taxdetails&id=104546 on 2019-03-02 ^a b c d e f g h i j k l m n o p q r s t u v w x y z aa ab ac ad ae af ag ah ai aj ak al am an ao ap aq ar as at au av aw ax ay az ba bb bc bd be bf bg bh bi bj bk bl bm bn bo bp bq br bs bt bu bv bw bx by bz ca cb cc cd ce cf cg ch ci cj ck cl cm cn co cp cq cr cs ct cu cv cw cx cy cz da db dc dd de df dg dh di dj dk dl dm dn do dp dq dr ds dt du dv dw dx Griffiths, Charles (1976).Guide to the Benthic Marine Amphipods of Southern Africa . Cape Town: South African Museum.ISBN 0-949940-85-2 ^a b c d e f Jones, Georgina (2008).A field guide to the marine animals of the Cape Peninsula . Cape Town: SURG.ISBN 978-0-620-41639-9 ^ Horton, T.; Lowry, J.; De Broyer, C.; Bellan-Santini, D.; Coleman, C. O.; Corbari, L.; Costello, M. J.; Daneliya, M.; Dauvin, J-C.; Fišer, C.; Gasca, R.; Grabowski, M.; Guerra-García, J. M.; Hendrycks, E.; Hughes, L.; Jaume, D.; Jazdzewski, K.; Kim, Y.-H.; King, R.; Krapp-Schickel, T.; LeCroy, S.; Lörz, A.-N.; Mamos, T.; Senna, A. R.; Serejo, C.; Sket, B.; Souza-Filho, J. F.; Tandberg, A.H.; Thomas, J.; Thurston, M.; Vader, W.; Väinölä, R.; Vonk, R.; White, K.; Zeidler, W. (2019). World Amphipoda Database. Africoecetes armatus (Griffiths, 1974). Accessed through: World Register of Marine Species at:http://www.marinespecies.org/aphia.php?p=taxdetails&id=491838 on 2019-03-01 ^ Horton, T.; Lowry, J.; De Broyer, C.; Bellan-Santini, D.; Coleman, C. O.; Corbari, L.; Costello, M. J.; Daneliya, M.; Dauvin, J-C.; Fišer, C.; Gasca, R.; Grabowski, M.; Guerra-García, J. M.; Hendrycks, E.; Hughes, L.; Jaume, D.; Jazdzewski, K.; Kim, Y.-H.; King, R.; Krapp-Schickel, T.; LeCroy, S.; Lörz, A.-N.; Mamos, T.; Senna, A. R.; Serejo, C.; Sket, B.; Souza-Filho, J. F.; Tandberg, A.H.; Thomas, J.; Thurston, M.; Vader, W.; Väinölä, R.; Vonk, R.; White, K.; Zeidler, W. (2019). World Amphipoda Database. Gammaropsis pseudodenticulata Ledoyer, 1979. Accessed through: World Register of Marine Species at:http://www.marinespecies.org/aphia.php?p=taxdetails&id=548580 on 2019-03-01 ^ Horton, T.; Lowry, J.; De Broyer, C.; Bellan-Santini, D.; Coleman, C. O.; Corbari, L.; Costello, M. J.; Daneliya, M.; Dauvin, J-C.; Fišer, C.; Gasca, R.; Grabowski, M.; Guerra-García, J. M.; Hendrycks, E.; Hughes, L.; Jaume, D.; Jazdzewski, K.; Kim, Y.-H.; King, R.; Krapp-Schickel, T.; LeCroy, S.; Lörz, A.-N.; Mamos, T.; Senna, A. R.; Serejo, C.; Sket, B.; Souza-Filho, J. F.; Tandberg, A.H.; Thomas, J.; Thurston, M.; Vader, W.; Väinölä, R.; Vonk, R.; White, K.; Zeidler, W. (2019). World Amphipoda Database. Aora inflata Griffiths, 1976. Accessed through: World Register of Marine Species at:http://www.marinespecies.org/aphia.php?p=taxdetails&id=488673 on 2019-03-01 ^ Horton, T.; Lowry, J.; De Broyer, C.; Bellan-Santini, D.; Coleman, C. O.; Corbari, L.; Costello, M. J.; Daneliya, M.; Dauvin, J-C.; Fišer, C.; Gasca, R.; Grabowski, M.; Guerra-García, J. M.; Hendrycks, E.; Hughes, L.; Jaume, D.; Jazdzewski, K.; Kim, Y.-H.; King, R.; Krapp-Schickel, T.; LeCroy, S.; Lörz, A.-N.; Mamos, T.; Senna, A. R.; Serejo, C.; Sket, B.; Souza-Filho, J. F.; Tandberg, A.H.; Thomas, J.; Thurston, M.; Vader, W.; Väinölä, R.; Vonk, R.; White, K.; Zeidler, W. (2019). World Amphipoda Database. Bemlos teleporus (K.H. Barnard, 1955). Accessed through: World Register of Marine Species at:http://www.marinespecies.org/aphia.php?p=taxdetails&id=488764 on 2019-03-01 ^ Horton, T.; Lowry, J.; De Broyer, C.; Bellan-Santini, D.; Coleman, C. O.; Corbari, L.; Costello, M. J.; Daneliya, M.; Dauvin, J-C.; Fišer, C.; Gasca, R.; Grabowski, M.; Guerra-García, J. M.; Hendrycks, E.; Hughes, L.; Jaume, D.; Jazdzewski, K.; Kim, Y.-H.; King, R.; Krapp-Schickel, T.; LeCroy, S.; Lörz, A.-N.; Mamos, T.; Senna, A. R.; Serejo, C.; Sket, B.; Souza-Filho, J. F.; Tandberg, A.H.; Thomas, J.; Thurston, M.; Vader, W.; Väinölä, R.; Vonk, R.; White, K.; Zeidler, W. (2019). World Amphipoda Database. Grandidierella nyala (Griffiths, 1974). Accessed through: World Register of Marine Species at:http://www.marinespecies.org/aphia.php?p=taxdetails&id=488816 on 2019-03-01 ^ Horton, T.; Lowry, J.; De Broyer, C.; Bellan-Santini, D.; Coleman, C. O.; Corbari, L.; Costello, M. J.; Daneliya, M.; Dauvin, J-C.; Fišer, C.; Gasca, R.; Grabowski, M.; Guerra-García, J. M.; Hendrycks, E.; Hughes, L.; Jaume, D.; Jazdzewski, K.; Kim, Y.-H.; King, R.; Krapp-Schickel, T.; LeCroy, S.; Lörz, A.-N.; Mamos, T.; Senna, A. R.; Serejo, C.; Sket, B.; Souza-Filho, J. F.; Tandberg, A.H.; Thomas, J.; Thurston, M.; Vader, W.; Väinölä, R.; Vonk, R.; White, K.; Zeidler, W. (2019). World Amphipoda Database. Incratella inermis (Ledoyer, 1967). Accessed through: World Register of Marine Species at:http://www.marinespecies.org/aphia.php?p=taxdetails&id=431265 on 2019-03-01 ^ Horton, T.; Lowry, J.; De Broyer, C.; Bellan-Santini, D.; Coleman, C. O.; Corbari, L.; Costello, M. J.; Daneliya, M.; Dauvin, J-C.; Fišer, C.; Gasca, R.; Grabowski, M.; Guerra-García, J. M.; Hendrycks, E.; Hughes, L.; Jaume, D.; Jazdzewski, K.; Kim, Y.-H.; King, R.; Krapp-Schickel, T.; LeCroy, S.; Lörz, A.-N.; Mamos, T.; Senna, A. R.; Serejo, C.; Sket, B.; Souza-Filho, J. F.; Tandberg, A.H.; Thomas, J.; Thurston, M.; Vader, W.; Väinölä, R.; Vonk, R.; White, K.; Zeidler, W. (2019). World Amphipoda Database. Victoriopisa chilkensis (Chilton, 1921). Accessed through: World Register of Marine Species at:http://www.marinespecies.org/aphia.php?p=taxdetails&id=535896 on 2019-03-01 ^ Horton, T.; Lowry, J.; De Broyer, C.; Bellan-Santini, D.; Coleman, C. O.; Corbari, L.; Costello, M. J.; Daneliya, M.; Dauvin, J-C.; Fišer, C.; Gasca, R.; Grabowski, M.; Guerra-García, J. M.; Hendrycks, E.; Hughes, L.; Jaume, D.; Jazdzewski, K.; Kim, Y.-H.; King, R.; Krapp-Schickel, T.; LeCroy, S.; Lörz, A.-N.; Mamos, T.; Senna, A. R.; Serejo, C.; Sket, B.; Souza-Filho, J. F.; Tandberg, A.H.; Thomas, J.; Thurston, M.; Vader, W.; Väinölä, R.; Vonk, R.; White, K.; Zeidler, W. (2019). World Amphipoda Database. Victoriopisa epistomata (Griffiths, 1974). Accessed through: World Register of Marine Species at:http://www.marinespecies.org/aphia.php?p=taxdetails&id=535899 on 2019-03-01 ^ Horton, T.; Lowry, J.; De Broyer, C.; Bellan-Santini, D.; Coleman, C. O.; Corbari, L.; Costello, M. J.; Daneliya, M.; Dauvin, J-C.; Fišer, C.; Gasca, R.; Grabowski, M.; Guerra-García, J. M.; Hendrycks, E.; Hughes, L.; Jaume, D.; Jazdzewski, K.; Kim, Y.-H.; King, R.; Krapp-Schickel, T.; LeCroy, S.; Lörz, A.-N.; Mamos, T.; Senna, A. R.; Serejo, C.; Sket, B.; Souza-Filho, J. F.; Tandberg, A.H.; Thomas, J.; Thurston, M.; Vader, W.; Väinölä, R.; Vonk, R.; White, K.; Zeidler, W. (2019). World Amphipoda Database. Austromaera bruzelii (Stebbing, 1888). Accessed through: World Register of Marine Species at:http://www.marinespecies.org/aphia.php?p=taxdetails&id=531400 on 2019-03-01 ^ Horton, T.; Lowry, J.; De Broyer, C.; Bellan-Santini, D.; Coleman, C. O.; Corbari, L.; Costello, M. J.; Daneliya, M.; Dauvin, J-C.; Fišer, C.; Gasca, R.; Grabowski, M.; Guerra-García, J. M.; Hendrycks, E.; Hughes, L.; Jaume, D.; Jazdzewski, K.; Kim, Y.-H.; King, R.; Krapp-Schickel, T.; LeCroy, S.; Lörz, A.-N.; Mamos, T.; Senna, A. R.; Serejo, C.; Sket, B.; Souza-Filho, J. F.; Tandberg, A.H.; Thomas, J.; Thurston, M.; Vader, W.; Väinölä, R.; Vonk, R.; White, K.; Zeidler, W. (2019). World Amphipoda Database. Austromaera mastersii (Haswell, 1879). Accessed through: World Register of Marine Species at:http://www.marinespecies.org/aphia.php?p=taxdetails&id=531369 on 2019-03-01 ^ Horton, T.; Lowry, J.; De Broyer, C.; Bellan-Santini, D.; Coleman, C. O.; Corbari, L.; Costello, M. J.; Daneliya, M.; Dauvin, J-C.; Fišer, C.; Gasca, R.; Grabowski, M.; Guerra-García, J. M.; Hendrycks, E.; Hughes, L.; Jaume, D.; Jazdzewski, K.; Kim, Y.-H.; King, R.; Krapp-Schickel, T.; LeCroy, S.; Lörz, A.-N.; Mamos, T.; Senna, A. R.; Serejo, C.; Sket, B.; Souza-Filho, J. F.; Tandberg, A.H.; Thomas, J.; Thurston, M.; Vader, W.; Väinölä, R.; Vonk, R.; White, K.; Zeidler, W. (2019). World Amphipoda Database. Othomaera komma (Griffiths, 1975). Accessed through: World Register of Marine Species at:http://www.marinespecies.org/aphia.php?p=taxdetails&id=534782 on 2019-03-01 ^ Horton, T.; Lowry, J.; De Broyer, C.; Bellan-Santini, D.; Coleman, C. O.; Corbari, L.; Costello, M. J.; Daneliya, M.; Dauvin, J-C.; Fišer, C.; Gasca, R.; Grabowski, M.; Guerra-García, J. M.; Hendrycks, E.; Hughes, L.; Jaume, D.; Jazdzewski, K.; Kim, Y.-H.; King, R.; Krapp-Schickel, T.; LeCroy, S.; Lörz, A.-N.; Mamos, T.; Senna, A. R.; Serejo, C.; Sket, B.; Souza-Filho, J. F.; Tandberg, A.H.; Thomas, J.; Thurston, M.; Vader, W.; Väinölä, R.; Vonk, R.; White, K.; Zeidler, W. (2019). World Amphipoda Database. Othomaera lobata (Griffiths, 1976). Accessed through: World Register of Marine Species at:http://www.marinespecies.org/aphia.php?p=taxdetails&id=534783 on 2019-03-01 ^ Horton, T.; Lowry, J.; De Broyer, C.; Bellan-Santini, D.; Coleman, C. O.; Corbari, L.; Costello, M. J.; Daneliya, M.; Dauvin, J-C.; Fišer, C.; Gasca, R.; Grabowski, M.; Guerra-García, J. M.; Hendrycks, E.; Hughes, L.; Jaume, D.; Jazdzewski, K.; Kim, Y.-H.; King, R.; Krapp-Schickel, T.; LeCroy, S.; Lörz, A.-N.; Mamos, T.; Senna, A. R.; Serejo, C.; Sket, B.; Souza-Filho, J. F.; Tandberg, A.H.; Thomas, J.; Thurston, M.; Vader, W.; Väinölä, R.; Vonk, R.; White, K.; Zeidler, W. (2019). World Amphipoda Database. Quadrimaera serrata (Schellenberg, 1938). Accessed through: World Register of Marine Species at:http://www.marinespecies.org/aphia.php?p=taxdetails&id=534878 on 2019-03-01 ^ Horton, T.; Lowry, J.; De Broyer, C.; Bellan-Santini, D.; Coleman, C. O.; Corbari, L.; Costello, M. J.; Daneliya, M.; Dauvin, J-C.; Fišer, C.; Gasca, R.; Grabowski, M.; Guerra-García, J. M.; Hendrycks, E.; Hughes, L.; Jaume, D.; Jazdzewski, K.; Kim, Y.-H.; King, R.; Krapp-Schickel, T.; LeCroy, S.; Lörz, A.-N.; Mamos, T.; Senna, A. R.; Serejo, C.; Sket, B.; Souza-Filho, J. F.; Tandberg, A.H.; Thomas, J.; Thurston, M.; Vader, W.; Väinölä, R.; Vonk, R.; White, K.; Zeidler, W. (2019). World Amphipoda Database. Ledoyeromelita excavata (Ledoyer, 1979). Accessed through: World Register of Marine Species at:http://www.marinespecies.org/aphia.php?p=taxdetails&id=991119 on 2019-03-01 ^a b c d e f g h i j k l m n o p q r s t u v w x y Day, Jennifer (1980). "South African Cumacea Part 4".Annals of the South African Museum .82 (6). Cape Town: South African Museum.ISBN 0-908407-99-8 ^a b c d e f g h i j k l m n o p q r s t u v w x y z aa ab ac ad ae af ag ah ai aj ak al am an ao ap aq ar as at au av aw ax ay az ba bb bc bd be bf bg bh bi bj bk bl bm bn bo bp bq br bs bt bu bv bw bx by bz ca cb cc cd ce cf cg ch ci cj ck cl cm cn co cp cq cr cs ct cu cv cw cx cy cz da db dc dd de df dg dh di dj dk dl dm dn do dp dq dr ds dt du dv dw dx dy dz ea eb ec ed ee ef eg eh ei ej ek el em en eo ep eq er es et eu ev ew ex ey ez fa fb fc fd fe ff fg fh fi fj fk fl fm fn fo fp fq fr fs ft fu fv fw fx fy fz ga gb gc gd ge gf gg gh gi gj gk gl gm gn go gp gq gr gs gt gu gv gw gx gy gz ha hb hc hd he hf hg Kensley, Brian (1978).Shrimps and Prawns of Southern Africa . Cape Town: South African Museum.ISBN 0-949940-01-1 ^ WoRMS (2019). Eusergestes arcticus (Krøyer, 1855). Accessed at:http://www.marinespecies.org/aphia.php?p=taxdetails&id=515738 on 2019-03-01 ^ Siegel, V. (Ed) (2019). World Euphausiacea Database. Euphausia americana Hansen, 1911. Accessed through: World Register of Marine Species at:http://www.marinespecies.org/aphia.php?p=taxdetails&id=110682 on 2019-03-01 ^ Siegel, V. (Ed) (2019). World Euphausiacea Database. Euphausia hanseni Zimmer, 1915. Accessed through: World Register of Marine Species at:http://www.marinespecies.org/aphia.php?p=taxdetails&id=110685 on 2019-03-01 ^ Siegel, V. (Ed) (2019). World Euphausiacea Database. Euphausia recurva Hansen, 1905. Accessed through: World Register of Marine Species at:http://www.marinespecies.org/aphia.php?p=taxdetails&id=221047 on 2019-03-01 ^a b c d e f g h i j k l m n o p q r s t u v w x y z aa ab ac ad ae af ag ah ai aj ak al am an ao ap aq ar as at au av aw ax ay az ba bb bc bd be bf bg bh bi bj bk bl bm bn bo bp bq br bs bt bu bv bw bx by bz ca cb cc cd ce cf cg ch ci cj ck cl cm cn co cp cq cr cs ct cu cv cw cx cy cz da db dc dd de df dg dh di dj dk dl dm dn do dp dq dr ds dt du dv dw dx dy dz ea eb ec ed ee ef eg eh ei ej ek el em en eo ep eq er es et eu ev ew ex ey ez fa fb fc fd fe ff fg fh fi fj fk fl fm fn fo fp fq fr fs ft fu fv fw fx fy fz ga gb gc gd ge gf gg gh gi gj gk gl gm gn go gp gq gr gs gt gu gv gw gx gy gz ha hb hc hd he hf hg hh hi hj hk hl hm hn ho hp hq hr hs ht hu hv hw hx hy hz ia ib ic id ie if ig ih ii ij ik il im in io ip iq ir is it iu iv iw ix iy iz ja jb jc jd je jf jg jh ji Kensley, Brian (1978).Guide to the Marine Isopods of Southern Africa . Cape Town: South African Museum.ISBN 0-908407-43-2 ^a b c Grindley, John R. (1980). "The Pseudodiaptomidae (Copepoda, Calanoida) of South African Waters, including a new species, Pseudodioptamus charteri".Annals of the South African Museum .XLVI (XV). Cape Town: South African Museum.
National taxon checklists
Plants
Animals Arthropods Arachnids Harvestmen Microwhip scorpions Pseudoscorpions Scorpions Shorttailed whipscorpions Solifugae Araneae Ixodida Whip spiders and tailless whip scorpions Insects Alderflies, dobsonflies and fishflies Beetles Booklice, barklice and barkflies Butterflies and moths Caddisflies Cockroaches and termites Dragonflies and damselflies Earwigs Fleas Flies Jumping bristletails Lice Mantises Mayflies Net-winged insects Notoptera Orthoptera Sawflies, wasps, bees, and ants Scorpionflies Silverfish and firebrats Stick and leaf insects Stoneflies Strepsiptera Termites Thrips True bugs Webspinners
Molluscs Vertebrates
Seaweeds Fungi Related
Regional taxon checklists and other minor lists
Biodiversity research in SA
Research Research Citizen science Botanical Taxonomists
Related
Regional biodiversity Legislation Publications
