Research Article |
Corresponding author: Neal L. Evenhuis ( neale@bishopmuseum.org ) Academic editor: Torsten Dikow
© 2015 Stephen A. Marshall, Neal L. Evenhuis.
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:
Marshall SA, Evenhuis NL (2015) New species without dead bodies: a case for photo-based descriptions, illustrated by a striking new species of Marleyimyia Hesse (Diptera, Bombyliidae) from South Africa. ZooKeys 525: 117-127. https://doi.org/10.3897/zookeys.525.6143
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A new bombyliid species Marleyimyia xylocopae Marshall & Evenhuis, sp. n., an apparent mimic of the carpenter bee Xylocopa flavicollis (De Geer), is described from South Africa on the basis of photographs only. The pros and cons of species descriptions in the absence of preserved type specimens are discussed.
South Africa, bee fly, mimicry, Xylocopa , type specimens, photography, taxonomy
“Collecting specimens is no longer required to describe a species or to document its rediscovery.”
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“Describing a new species without depositing a holotype when a specimen can be preserved borders on taxonomic malpractice.”
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A recent paper in Science by
First of all, let us reiterate the obvious reasons that collecting specimens is highly desirable, and briefly consider and reject arguments against collecting. Specimens are indeed the ‘gold standard’ for species descriptions. Not only do they allow for consideration of a full suite of characters including internal morphology, microscopic and genetic characters, they preserve data for future access with future technologies and future questions. Specimen collections are our greatest treasure trove of biodiversity information and continued collection development must remain a priority. Arguments against specimen collections usually pivot on the potential impact of collecting on fragile populations. Such arguments are weak, since there are vanishingly few examples of scientific collecting having a detrimental effect at the population or species levels and there are very few circumstances under which the removal of a few individuals from a population might seriously harm the ultimate survival of the species. Most, by orders of magnitude, of the animal species awaiting description are invertebrates, and it is especially difficult to make a case against invertebrate collecting on the basis of conservation biology. As invertebrate taxonomists, we therefore agree with the letter of
As explained by
Even in the absence of a collected type specimen, current technologies such as high-resolution photography can often provide enough information for a proper description resulting in a readily recognizable and unequivocally distinct newly named species, and in some cases can provide more information (such as colour, soft parts, delicate structures, posture, behaviour) than could be extracted from a preserved specimen. The few previous descriptions of extant new species without a type (or part thereof) have for the most part been restricted to large vertebrates, for example primate species known from only small populations (
In the example provided here, a highly distinctive fly species belonging to an extremely rare genus (only three other known specimens of two species) was photographed on two occasions and then collected in the field, but the captured individual escaped before it could be preserved as a traditional dead type specimen. Our description, based on photographs of two different living flies, is complete and adequate to identify this species and adds an interesting and easily recognized species to the literature. It not only increases our knowledge of the biodiversity of the area in which it was collected and of the genus in which it is placed but, as we explain below, also provides some interesting ecological and biological information.
The situation leading to this approach is a simple one to understand, since it pivots on an accidentally lost type specimen that might not be collected again due to its rarity. Although this description is by definition singular because it is the first of its kind (at least for Diptera), we predict that a growth in descriptions without physical type specimens is inevitable, and that this growth will result not as much from accidental loss of specimens as from increasing restrictions on collecting. Every taxonomist has been in the position of completing a revision that needs to be rounded out with species from places from which specimens are difficult or impossible to obtain, often because of laws preventing collection or export of specimens. For many of these required taxa, the solution to this problem is for the taxonomist to instead “collect” digital images that, in the case of new species, can represent type specimens. We are not arguing that this practice is generally desirable, only that it is inevitable and increasingly practical when diagnostic characters are distinct and discernable through photographs.
Another trend pushing us inexorably to a wider acceptance of species descriptions without physical type specimens is the rapid growth of extensive, high quality digital image collections dissociated from collections of physical specimens (Marshall, in press). As these image collections become curated just as dead specimens are curated today, these digital “specimens” will find their way into the work of practicing taxonomists, and they will need names. At a time when we need more than ever to identify the biodiversity of this planet before it disappears, it is unrealistic to think that distinct and diagnosable new taxa known only from good photographs and appropriate associated metadata should be organized and referred to only as “undescribed species #nnn”, when they can and should be organized and named using the existing rules of nomenclature.
In recognizing the need to name species without dead type specimens we are not arguing for a loosening of taxonomic standards. In fact, we expect that descriptions unsupported by existing physical type specimens will be subject to especially critical scrutiny by skeptical editors and responsible reviewers. We expect that such descriptions that do not render new species unequivocally recognizable will be rejected, just as they should be if they were based on dead type specimens. Once published, digital representations of type specimens will be much more widely available for use and scrutiny than physical type specimens archived in distant museums.
The species described below was photographed in nature using a Nikon D800 with a 105 macro lens and a hand-held flash. The holotype specimen was not captured, so the image presented serves as representation of the holotype. Morphological terminology follows
Marleyimyia Hesse, 1956: 521. Type species: Marleyimyia natalensis Hesse, 1956, by original designation.
Marleyimyia Hesse, 1956 was originally described based on a single male specimen with vestigial mouthparts and bred from a log containing cossid larvae. The genus is currently known from only three specimens representing two described species from widely disjunct localities: Marleyimyia goliath (Oldroyd) from Peninsular Malaysia and M. natalensis Hesse from southern Africa. In proposing his new genus,
REPUBLIC OF SOUTH AFRICA: KwaZulu Natal: Ndumo Nature Preserve, Ndumo Campground, 26°54'31.07"S; 32°18'57.85"E.
Holotype female from SOUTH AFRICA: KwaZulu Natal: Ndumo Nature Preserve, Ndumo Campground, 26°54'31.07"S; 32°18'57.85"E, 74.0 m elev., 1 Dec 2014, S.A. Marshall. Holotype represented in photograph No. 7007 (Fig.
Separated from its congeners by the all black infuscated wing (hyaline in M. goliath and M. natalensis), and the mesonotal pattern of black hairs anteriorly and yellow hairs posteriorly (entirely black-haired in M. goliath and predominantly yellowish brown-haired in M. natalensis).
Female. Body: ca. 18–20 mm in length (extrapolated from comparison of grass blade width of Eremochroa (centipede grass) in a larger habitus photograph [No. 7009]). Head (Fig.
Right antenna of Marleyimyia species. A M. xylocopae Marshall & Evenhuis, sp. n. B M. goliath (Oldroyd) [from
Thorax. Mesonotum and pleura shining black in ground color (scutellum ground color obscured); mesonotum with dense short “clipped-looking” black pile anteriorly to level of wing base, yellow pile from wing base to posterior edge of mesonotal disc including postalar calli, long, shaggy laterally, short and “clipped-looking” on disc; scutellum densely shaggy yellow pilose; pleura thickly black haired, those hairs on anepisternum with dark brownish sheen. (Halter and pleural area under wing obscured in photos).
Legs. (Hind femur obscured in photographs). Fore and mid legs (and hind legs beyond femur) black with a shiny greasy appearance, some bluish highlights on femora and tarsi. Fore and mid femora short, stout, with long black hairs ventrally, longest basally, tapering to shorter apical hairs; tibiae shorter than femora, with short black spicules.
Wing (Fig.
Abdomen. Broad, ovular in shape, shining black in ground color with bluish highlights (sternites not visible); tergite II and III with admixed short silvery white hair and tomentum dorsolaterally and sparse silvery tomentum with bluish highlights dorsomedially; tergites IV–VII with adpressed black tomentum and sparse silvery white tomentum dorsomedially. Genitalia. Not dissected.
Two different specimens were photographed (one at each locality indicated above). That they are different is evidenced by the rubbed frons in the Red Cliffs paratype (photos taken on 27 November) and that the photos taken later at the Campground site (on 1 December) were of a specimen without a rubbed frons. This new species shares its unusual large body, wing shape, wing venation, and antennal flagellomere shape with M. goliath, which occurs in Peninsular Malaysia. These characters differ from the smaller and more slender type species, Marleyimyia natalensis (Fig.
The striking yellow and black vestiture pattern on the thorax and abdomen, and the body shape, are unusual in bombyliids and show a remarkable similarity to xylocopid bees. The model for this possible case of Batesian mimicry appears to be Xylocopa flavicollis (De Geer), which was also photographed at around the same time in the Ndumo area (Fig.
Map (http://www.simplemappr.net/map/4577) showing the known localities of Marleyimyia natalensis Hesse and M. xylocopae sp. n., in Kwa-Zulu Natal, South Africa.
We thank and Nigel Wyatt (BMNH) for kindly providing photos of M. goliath and the undescribed Nigerian Marleyimyia. Burgert Muller kindly checked the KwaZulu-Natal Museum for possible collected specimens of M. xylocopae. The observations that made this paper possible were made during the KwaZulu Natal Expedition 2014, organized by A.H. Kirk-Spriggs (National Museum, Bloemfontein, South Africa) and V.R. Swart (University of the Free State, Bloemfontein, South Africa).