Research Article |
Corresponding author: Adrian John Armstrong ( aandcarmstrong@gmail.com ) Academic editor: Burgert Muller
© 2019 Adrian John Armstrong, Martin H. Villet.
This is an open access article distributed under the terms of the Creative Commons Attribution License (CC BY 4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Citation:
Armstrong AJ, Villet MH (2019) Checklist, endemism, English vernacular names and identification of the cicadas (Insecta, Hemiptera, Cicadidae) of KwaZulu-Natal, South Africa. African Invertebrates 60(2): 165-193. https://doi.org/10.3897/afrinvertebr.60.35130
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Public understanding of the goals of applied biology and conservation is promoted by showcasing charismatic or significant organisms using vernacular names. Conservation activities in the province of KwaZulu-Natal, South Africa, are prioritising taxa that have high rates of provincial endemism, such as snails, earthworms, millipedes and cicadas. To assist wider public engagement in these activities, an assessment of endemism of the cicadas of KwaZulu-Natal is presented along with a dichotomous, 37-couplet key for the identification of males, based mainly on externally visible morphology and colouration. Standardised English vernacular names coined following a simple naming convention are proposed. Forty-two percent (16 out of 38) of the cicada species known from KwaZulu-Natal are endemic to the province. Photographs of some of the species are included to facilitate their identification. Photographs can be used for identification of various species providing that the diagnostic characters are visible in the photographs. For this purpose, photographs may have to be taken of hand-held individuals. Some of the endemic species are of particular concern for conservation because they are not known to occur in statutory protected areas or are only known from relatively small protected areas. The latter may not be able to ensure the long-term survival of the species. The rate and extent of loss of habitat outside protected areas is likely to be a grave threat to species that are not protected or that are inadequately conserved in statutory protected areas. The standardised vernacular names proposed here provide a tool for communicating provincial conservation plans and concerns with stakeholders in KwaZulu-Natal and for stimulating interest in cicadas amongst land users, environmental impact assessment practitioners, biologists, naturalists and citizen scientists.
common names, key to species, diagnostic characters, conservation assessment, cicada photographs, vulnerability to extinction
Professional biological conservation includes integrating the requirements of endemic species into conservation planning and environmental impact assessments (
The system of universal scientific names endeavours to eliminate ambiguity about the identity of the organism being named (
Internationally, the charismatic bugs known as cicadas in English and as isihlonono, isidlonono, inyekevu or isibawu in Zulu (
Occurrence data from the collections of the Africa Museum (Tervuren), the Albany Museum (Makhanda [Grahamstown]), the Ditsong National Museum of Natural History (Pretoria), the Durban Natural Science Museum (Durban), the Iziko South African Museum (Cape Town), the KwaZulu-Natal Museum (Pietermaritzburg), the South African National Collection of Insects (Pretoria), the Natural History Museum of Zimbabwe (Bulawayo), the Natural History Museum (London), the Swedish Museum of Natural History (Stockholm), the National Museum of Namibia (Windhoek), donations from many members of the public and a spectrum of published literature, were collated by MHV and supplemented by the Ezemvelo KZN Wildlife Biodiversity Database. These allowed the compilation of a checklist of species known from KwaZulu-Natal and an assessment of which species are likely to be endemic to that province.
A fundamental guideline to coining standardised scientific names for organisms is articulated in Recommendation 25C of the International Code of Zoological Nomenclature: “… ensure that they are chosen with their subsequent users in mind and that, as far as possible, they are appropriate, compact, euphonious, memorable and do not cause offence” (
Some vernacular names already exist in folk taxonomies and published literature. If appropriate, these should be used because those organisms are sufficiently familiar and significant to have attracted public attention. Additionally, there is no advantage to creating a synonym. However, homonyms and clearly inapplicable vernacular names should be replaced by appropriate new names. Folk taxonomies contain many names that are equivalent to scientific taxa such as families (e.g. cicada), but seldom recognise the individual species comprising these groups. In these cases, vernacular neologisms can be formed by qualifying the collective name with a suitable translation of the species-specific part of the scientific name. Some scientific names of genera are derived from vernacular words, e.g. Ibonikawhite, Stagira, Munza and Monomatapa. Reciprocally, where a particular taxon, such as a genus or family, lacks a vernacular name, one can be formed from the scientific name. Translation has the advantage of coordinating continuity between vernacular and scientific names. If a robust and stable phylogenetic classification of a group has been established (e.g.
New vernacular names for taxa such as families, genera and species can also be formed from diagnostic or characteristic features of the taxon under consideration. Examples of these features include morphology, colouration, calls or song and ecological relationships.
We have used these principles in the creation of English names for cicada species occurring in KwaZulu-Natal. These and other naming conventions (e.g.
Based on the species list, relevant taxonomic literature (e.g.
Over 7800 records of cicadas occurring in southern Africa were gathered, including over 800 records of cicadas from at least 368 unique locations in KwaZulu-Natal. Following the classification of
Most of the larger-bodied cicadas (Cicadinae) are found in several provinces of South Africa, but are endemic to the country (Table
Checklist of cicada species occurring in KwaZulu-Natal, South Africa, with proposed vernacular names. Species endemic to KwaZulu-Natal are set in bold print. KZN = KwaZulu-Natal, RSA = Republic of South Africa.
Scientific Name | Endemism | English Name |
---|---|---|
Subfamily TETTIGOMYIINAE Distant, 1905 | Africa | Obscure Cicadas (universally diagnostic characters lacking) |
Tribe TETTIGOMYIINI Distant, 1905 | Africa | Pygmy Bladder Cicadas |
Genus Stagira Stål, 1861 | Southern Africa | Redeye Cicadas |
Stagira dracomontana Villet, 1997 | KZN | Small Drakensberg Redeye Cicada (Fig. |
Stagira dracomontanoides Villet, 1997 | KZN | Drakensberg Redeye Cicada |
Stagira empangeniensis Villet, 1997 | KZN | Empangeni Redeye Cicada (Fig. |
Stagira eshowiensis Villet, 1997 | KZN | Eshowe Redeye Cicada |
Stagira microcephala (Walker, 1850) | KZN | Smallhead Redeye Cicada (Fig. |
Stagira nasuta Villet, 1997 | KZN | Pointyhead Redeye Cicada |
Stagira natalensis Villet, 1997 | KZN | Savanna Redeye Cicada (Fig. |
Stagira ngomiensis Villet, 1997 | KZN | Ngome Redeye Cicada (Fig. |
Stagira nkandlhaensis Villet, 1997 | KZN | Nkandla Redeye Cicada (Fig. |
Stagira pondoensis Villet, 1997 | RSA | Pondoland Redeye Cicada (Fig. |
Stagira pseudaethlius Villet, 1997 | KZN | False Guineagrass Redeye Cicada |
Stagira purpurea Villet, 1997 | KZN | Purple Redeye Cicada (Fig. |
Stagira virescens Kirkaldy, 1909 | KZN | Guineagrass Redeye Cicada (Fig. |
Stagira xenomorpha Villet, 1997 | KZN | Strange Redeye Cicada |
Stagira zuluensis Villet, 1997 | KZN | Zulu Redeye Cicada |
Tribe MALAGASIINI Marshall et al., 2018 | Africa | Madagascar Cicadas (notably includes Malagasy species) |
Genus Quintilia (Stål, 1866) | RSA | Karoo Cicadas |
Quintilia sp. | RSA | Pied Cicada (Fig. |
Genus Nyara Villet, 1999 | RSA | Fainting Cicadas (feign death) |
Nyara thanatotica Villet, 1999 | RSA | Drab Fainting Cicada |
Subfamily CICADINAE Latreille, 1802 | Most of World | Baffled Cicadas (a baffle covering each sound-producing organ) |
Tribe PLATYPLEURINI Schmidt, 1918 | Africa and Asia | Broadwing Cicadas |
Genus Pycna Amyot & Audinet-Serville, 1843 | Africa | Large Tree Cicadas |
Pycna natalensis Distant, 1905 | RSA | Large Woodland Cicada |
Pycna semiclara (Germar, 1834) | RSA | Whining Forest Cicada (Fig. |
Genus Kongota Distant, 1904 | RSA | Greenwing Cicadas (predominant hindwing colour) |
Kongota punctigera (Walker, 1850) | RSA | Greenwing Cicada (Fig. |
Genus Munza Distant, 1904 | Africa | Broadborder Cicadas (broad hindwing margins) |
Munza basimacula (Walker, 1850) | Southern Africa | Small Broadborder Cicada |
Genus Brevisiana Boulard | Africa | Thorntree Cicadas (thorntree hostplants) |
Brevisiana brevis (Walker, 1850) | Southern Africa | Shrill Thorntree Cicada (Fig. |
Genus Oxypleura Amyot & Audinet-Serville, 1843 | Africa | Sharpcollar Cicadas (laterally-pointed thoracic collar) |
Oxypleura lenihani Boulard, 1985 | Southern Africa | Coastal Sharpcollar Cicada |
Genus Platypleura Amyot & Audinet-Serville, 1843 | Africa | Orangewing Cicadas (predominant hindwing colour) |
Platypleura argentata Villet, 1987 | RSA | Coastal Milkwood Orangewing Cicada |
Platypleura deusta (Thunberg, 1822) | RSA | Ouhout Orangewing Cicada (Fig. |
Platypleura divisa (Germar, 1834) | RSA | Centrestripe Orangewing Cicada |
Platypleura haglundi (Stål, 1866) | Southern Africa | Variable Orangewing Cicada |
Platypleura maytenophila Villet, 1987 | RSA | Spikethorn Orangewing Cicada |
Platypleura wahlbergi (Stål, 1855) | RSA | Zigzag Orangewing Cicada |
Platypleura zuluensis Villet, 1987 | RSA | Dune Koko Orangewing Cicada (Fig. |
Genus Tugelana Distant, 1912 | Southern Africa | Maputaland Orangewing Cicadas |
Tugelana butleri Distant, 1912 | Southern Africa | Maputaland Orangewing Cicada (Fig. |
Subfamily CICADETTINAE Buckton, 1890 | Most of World | Largeclasper Cicadas (relatively large male mating claspers) |
Tribe CICADETTINI Buckton, 1890 | Most of World | True Largeclasper Cicadas |
Genus Melampsalta Kolenati, 1857 | Unknown | Black-and-Brown Grassland Cicadas |
Melampsalta leucoptera (Germar, 1830) | RSA | Whitewing Grassland Cicada (Fig. |
Melampsalta limitata (Walker, 1852) | RSA | Clearwing Grassland Cicada |
Tribe PARNISINI Distant, 1905 | Unknown | Short Abdomen Cicadas |
Genus Zouga Distant, 1906 | Africa | Narrowwing Cicadas |
Zouga sp. | ?RSA | Dark Narrowwing Cicada |
Genus Taipinga Distant, 1905 | Southern Africa | Groovehead Cicadas |
Taipinga luctuosa (Stål, 1855) | KZN | Dismal Cicada |
Taipinga albivenosa (Walker, 1858) | KZN | Whitevein Cicada |
Tribe LAMOTIALNINI Boulard,1976 | Unknown | Widehead Cicadas (eyes laterally protruding forming a broad head) |
Genus Trismarcha Karsch, 1891 | Africa | Smoothfront Widehead Cicadas (top and front of head continuous) |
Trismarcha sirius (Distant, 1899) | Southern Africa | Small Widehead Cicada |
Genus Monomatapa Distant, 1897 | Africa | Anglefront Widehead Cicadas (top of head meets the front at an angle) |
Monomatapa insignis Distant, 1897 | Southern Africa | Large Widehead Cicada |
To date, very few vernacular names for African cicadas have been recognised and they all equate to Cicadidae, i.e. the taxonomic rank of family in scientific nomenclature. Cicadas collectively have been referred to as isibawu or inyenzane in Xhosa (
The inappropriate name Christmas Beetle, which is used for cicadas (which are bugs) in parts of South Africa and elsewhere, is a homonym that is also and more properly used for some local ruteline and melolonthine Chafer Beetles. Christmas Beetle has also recently been used for eumolpine Leaf Beetles by
Our proposed list of English names of cicadas occurring in KwaZulu-Natal is presented in Table
Cicadas are best located through the calling of the males. Calls of male cicadas differ between species (
The Stagira species with red colouration can be identified by a combination of general appearance and locality. For these species, georeferenced photographs of the whole animal may be used for identification. The other Stagira species would require good macrophotography of the various diagnostic features (see the taxonomic key below) to be identifiable from photographs. The habitat and locality where the Stagira cicada was photographed would be important confirmatory information.
Adult males of all of the species can be identified with the following taxonomic key. Many of the features mentioned are visible to the naked eye or with the use of a hand lens, but the use of a microscope is required to see microscopic hairs and certain structures of the genitalia of the Stagira species. Females’ opercula are smaller and their external genitalia simpler in comparison with males of the same species and they lack timbals (e.g. compare male and female in Figure
The nymphs of cicadas tend to live underground, are seldom seen and are very poorly known in South Africa (
1 | Abdomen forming about half of total body length and with a lateral flap covering the timbals; thorax with pronotum bearing distinct lateral lobes and metanotum hidden by mesonotum; forewing membrane usually opaque; largest spine on forefemur lying flat against the femur (Fig. |
3 |
– | Abdomen forming about two-thirds or more of total body length; timbals exposed, not hidden by a flap; thorax with pronotum lacking lateral lobes and metanotum at least partially visible behind mesonotum; forewing membrane more or less transparent; largest spine on forefemur standing more or less perpendicular to the femur (Fig. |
2 |
2 | Claspers present (Fig. |
16 |
– | Claspers absent; forewing with median and anterior cubital veins distinctly separated at their bases (Fig. |
22 |
3 | Hindwing with marginal membrane unusually wide, about 20% of hindwing length; small species, forewing length 16–17 mm | Munza basimacula |
– | Hindwing with marginal membrane narrow (Fig. |
4 |
4 | Membranes of both wings largely transparent, practically unpigmented | 5 |
– | Membranes of forewing and at least half of hindwing pigmented | 6 |
5 | Larger species (forewing length 33–40 mm), pronotum with large, pointed lateral lobes; forewing veins not spotted | Oxypleura lenihani |
– | Smaller species (forewing length 27–31 mm), pronotum with smaller, rounded lateral lobes; forewing veins usually with white spots | Brevisiana brevis |
6 | Hindwing largely greenish, without a black margin | 7 |
– | Hindwing mostly orange, with a black margin Platypleura and Tugelana | 9 |
7 | Smaller species (forewing length 26–28 mm); hindwing entirely pigmented; costal margin of forewing strongly dilated at base | Kongota punctigera |
– | Larger species (forewing length > 35 mm); hindwing transparent at apex; costal margin of forewing not strongly dilated at base (Fig. |
8 |
8 | Frons not deeply indented above clypeus | Pycna natalensis |
– | Frons deeply indented above clypeus (Fig. |
Pycna semiclara |
9 | Opercula (Fig. |
Platypleura argentata |
– | Opercula overlapping; forewing not silvery; white band around tip of abdomen either entire or divided longitudinally | 10 |
10 | Crossveins (Fig. |
11 |
– | Crossveins of hindwing not blackened; not associated with Anglestem Spikethorn plants | 12 |
11 | Body with brownish markings; black margin on hindwing well developed; forewing length 27–30 mm | Platypleura divisa |
– | Body with green markings; black margin on hindwing weakly developed; forewing length 28–31 mm | Platypleura maytenophila |
12 | Smaller species (forewing length < 23 mm) | 13 |
– | Larger species (forewing length > 25 mm) | 15 |
13 | Hindwing with dark markings not restricted to margin; forewing with relatively rounded angles, costal margin weakly curved at base | 14 |
– | Hindwing with black pigmentation restricted to margin; forewing quite angular, costal margin strongly curved at base | Platypleura haglundi |
14 | Forewing without transparent areas and plainly pigmented; apical cells of hindwing darkened in their centres like wing margin | Tugelana butleri |
– | Forewing with transparent areas near the margin and usually variegated; apical cells of hindwing orange in their centres, leaving a dark zigzag marking along the discal crossveins | Platypleura wahlbergi |
15 | Pronotum lacking black median line; associated with the plant Maytenus procumbens (Dune Koko Tree) in coastal areas | Platypleura zuluensis |
– | Pronotum with distinct, black median line; associated with the plant Leucosidea sericea (Ouhout) in montane areas | Platypleura deusta |
16 | Abdomen pale brownish with black markings Cicadettini: Melampsalta | 18 |
– | Abdomen more plainly coloured, green, reddish, purple or darker brown | 17 |
17 | Eyes not distinctly projecting beyond anterior angles of pronotum (Fig. |
19 |
– | Eyes distinctly projecting beyond anterior angles of pronotum Lamotialnini | 21 |
18 | Forewings somewhat opaque, whitish, pigmented around some veins; abdomen somewhat inflated | Melampsalta leucoptera |
– | Forewings hyaline, not pigmented around veins; abdomen relatively slim | Melampsalta limitata |
19 | Hindwings with six apical cells (Fig. |
Zouga sp. |
– | Hindwings with five apical cells Taipinga | 20 |
20 | Larger species, body ~17 mm long; wing veins brown | Taipinga luctuosa |
– | Smaller species, body ~12 mm long; wing veins white | Taipinga albivenosa |
21 | Smaller species, forewing length < 30 mm | Trismarcha sirius |
– | Larger species, forewing length > 35 mm | Monomatapa insignis |
22 | Abdominal tergites smoothly arched, without a median ridge Malagasiini | 23 |
– | Abdominal tergites with a median longitudinal ridge (Fig. |
24 |
23 | Forewings ovoid, somewhat rounded, about twice as long as wide | Quintilia sp. |
– | Forewings narrowly ellipsoid, somewhat pointed, about three times as long as wide | Nyara thanatotica |
24 | Dorsum of pygofer (Fig. |
25 |
– | Dorsum of pygofer smooth or humped (Fig. |
27 |
25 | Larger species, forewing length > 14 mm; costal vein red in mature specimens | Stagira pondoensis |
– | Smaller species, forewing length < 13 mm; costal vein green. | 26 |
26 | Timbal with four ribs (Fig. |
Stagira virescens |
– | Timbal with five ribs | Stagira pseudaethlius |
27 | Abdominal tergites bearing at least some pale, minute hairs. Generally medium-to-large sized [wing length 13–23 mm, females sometimes smaller] and/or with some red pigment | 28 |
– | Abdominal tergites without any pale hairs, but minute, usually dense, black hairs may be present. Generally small-to-medium sized [wing length 10–16 mm], green species | 34 |
28 | Urite spatulate (Fig. |
Stagira xenomorpha |
– | Urite not spatulate, margins of urite drawn into points near the mid-length (Fig. |
29 |
29 | Points on lateral margins of urite not hooked or recurved (Fig. |
Stagira ngomiensis |
– | Points on lateral margins of urite recurved or hooked (Fig. |
30 |
30 | Body generally with red or purple pigmentation; apical margin of urite sinuous; aedeagal keel ending in a vane (Fig. |
31 |
– | Body green, never with red or purple pigmentation; apical margin of urite smoothly semi-circular (Fig. |
32 |
31 | Timbal with four ribs; medial corner of operculum angular; escarpment region northwest of Pietermaritzburg | Stagira purpurea |
– | Timbal with three ribs; medial corner of operculum rounded; Nkandla Forest region | Stagira nkandlhaensis |
32 | Urite shield-like (Fig. |
Stagira eshowiensis |
– | Urite axe-like (Fig. |
33 |
33 | Head rounded (Fig. |
Stagira microcephala |
– | Head triangular (Fig. |
Stagira nasuta |
34 | Urite diamond-shaped (Fig. |
Stagira empangeniensis |
– | Urite shaped like arrowheads (Fig. |
35 |
35 | Lateral lobes of pygofer parallel in ventral view (Fig. |
36 |
– | Lateral lobes of pygofer diverging laterally in ventral view (Fig. |
37 |
36 | Clypeal profile convex and inflated (Fig. |
Stagira natalensis |
– | Clypeal profile straight (Fig. |
Stagira zuluensis |
37 | Length of forewing > 14.5 mm; apical cell of forewing rectangular | Stagira dracomontanoides |
– | Length of forewing < 13.5 mm; apical cell of forewing trapezoidal (Fig. |
Stagira dracomontana |
Forty-two percent of the cicada species of KwaZulu-Natal are endemic to the province (Table
The rate of land transformation that is occurring outside protected areas in the province is high; the recorded average rate of loss of natural habitat between 1994 and 2011 was 1.2% per annum (
All of the cicada species endemic to KwaZulu-Natal, for which accurate distribution information is available, are included in the current systematic conservation plan for KwaZulu-Natal (
We thank the curators of the Africa Museum (Tervuren), the Albany Museum (Makhanda [Grahamstown]), the Ditsong National Museum of Natural History [formerly Transvaal Museum] (Pretoria), the Durban Natural Science Museum (Durban), the Iziko South African Museum (Cape Town), the KwaZulu-Natal Museum (Pietermaritzburg), the South African National Collection of Insects (Pretoria), the Natural History Museum of Zimbabwe (Bulawayo), the Natural History Museum (London), the Swedish Museum of Natural History (Stockholm), the National Museum of Namibia (Windhoek) and Ezemvelo KZN Wildlife for access to specimens and data in their care; numerous members of the public for reporting records; Rhodes University and the National Research Foundation (NRF) of South Africa for financial support to MHV over several years; and Ezemvelo KZN Wildlife and Rhodes University for assisting with the research and publication of this work. We thank Debbie Jewitt, Tony Rebelo and Riaan Stals for fruitful discussion regarding vernacular names. Three reviewers improved the manuscript, for which they are thanked. The ideas, arguments and opinions expressed in this manuscript are those of the authors and do not necessarily represent those of Ezemvelo KZN Wildlife or the NRF.