Proceedings of the Eighth Forum Herbulot 2014. How to Accelerate the Inventory of Biodiversity (Schlettau, 30 June – 4 July 2014)

©Zoologische Staatssammlung München/Verlag Friedrich Pfeil; download www.pfeil-verlag.de

SPIXIANA 37 2 239-266 München, Dezember 2014 ISSN 0341-8391

Proceedings of the eighth Forum Herbulot 2014. How to accelerate the inventory of biodiversity (Schlettau, 30 June – 4 July 2014)

Axel Hausmann (ed.)

Hausmann, A. (ed.) 2014. Proceedings of the eighth Forum Herbulot 2014. How to accelerate the inventory of biodiversity (Schlettau, 30 June – 4 July 2014). Spixi- ana 37 (2): 239-266. The eighth Forum Herbulot 2014 in Schlettau, Germany, focused on modern tools and techniques to accelerate the assessment of global biodiversity without losing accuracy and quality of publications. New studies, projects and results from lepidopteran research were presented in thirty-two lectures. The results of the presentations and discussions were entered in a “Declaration on Accelerated Bio- diversity Assessment”. Axel Hausmann, SNSB – ZSM, Bavarian State Collection of Zoology, Münch- hausenstr. 21, 81247 Munich, Germany; e-mail: [email protected]

Short report and results

Axel Hausmann

Hausmann, A. 2014. Short report and results. Pp. 239-240 in: Hausmann, A. (ed.). Proceedings of the eighth Forum Herbulot 2014. How to accelerate the inventory of biodiversity (Schlettau, 30 June – 4 July 2014). Spixiana 37 (2). Axel Hausmann, SNSB – ZSM, Bavarian State Collection of Zoology, Münchhausenstr. 21, 81247 Munich, Germany; e-mail: [email protected]

Altogether 61 participants from 25 countries were and Taxonomy”), Lyubomir Penev (“Streamlining registered for the eighth Forum Herbulot (see Forum descriptions of new species identified with barcode Herbulot 2014, http//www.herbulot.de/) and were data”), Sujeevan Ratnasingham (“The BIN system: welcomed at a “Bavaro-Thuringian Barbecue”. The Standardizing molecular operational taxonomy in 32 presentations during six sessions were chaired animals”), Jeremy deWaard (“From BINs to Biodi- by Scott Miller (Washington, USA), Axel Hausmann versity: Rapid Arthropod Assessments using DNA (Munich, Germany), Jeremy deWaard (Guelph, Barcodes”), Scott Miller (“DNA barcode enabled Canada), Pasi Sihvonen (Helsinki, Finland), Cath- ecological research on Geometridae in Papua New erine Byrne (Hobart, Australia), and Hossein Rajaei Guinea”) and Hermann Staude (“Accelerating the in- (Hamburg, Germany). ventory of Lepidoptera early stages and host-plant & The conference started with presentations and other associations, by using citizen-science projects”). break-out discussions on how global biodiversity The results of the presentations and discussions were assessment could be accelerated and improved. entered in a Forum Herbulot declaration (see below) Chairman Axel Hausmann presented briefly Claude reflecting our consensual community position. The Herbulot’s strategy of producing a large number of seminary sessions of the second and the third day species descriptions. The following keynote talks covered also phylogenetic, taxonomic, zoogeo- included contributions of Michael Balke (“Tax- graphic, faunistic and other topics. Forum Herbulot onomy: Faster. Better”), Ellinor Michel (“Global 8 offered pleasant opportunities for collecting in the Digital Infrastructure for Biological Nomenclature Ore Mountains during all evenings of the meeting.

239 ©Zoologische Staatssammlung München/Verlag Friedrich Pfeil; download www.pfeil-verlag.de

Participants expressed their thanks to the organ- dinner in a restaurant in downtown Chemnitz. izers and sponsors (e. g. DFG HA 1806/11-1) of Fo- Forum Herbulot 8 came to an end with a one-day rum Herbulot 8 (2014). The research initiative Forum post-conference trip to Dresden: more than 30 par- Herbulot was, once again, generally welcomed and ticipants visited the Natural History Museum and the need for, and the advantages of, close scientific enjoyed sight-seeing during a guided boat tour on cooperation among geometrid experts were stressed. the Elbe river (see footnote below). In the evening, A proposal to have the next Forum Herbulot 9 in a smaller group attended the opera “Il barbiere di Concepción, Chile, mid-January 2017 was generally Siviglia” at the famous “Semper-Oper”. appreciated. Chairman Axel Hausmann reported Forum Herbulot 2014. Web-page of the International Sci- that future venues have been offered by the museums entific Community with research focussed on Geo in Stuttgart (Germany) and in South Korea. metridae. www.herbulot.de [accessed 06-Oct-2014] The conference was closed after the conference

A footnote to the report on the post-conference tour to Dresden

Manfred Sommerer

Sommerer, M. 2014. A footnote to the report on the post-conference tour to Dresden. Pp. 240-241 in: Hausmann, A. (ed.). Proceedings of the eighth Forum Herbulot 2014. How to accelerate the inventory of biodiversity (Schlettau, 30 June – 4 July 2014). Spixiana 37 (2). Manfred Sommerer, Volpinistr. 72, 80638 Munich, Germany; e-mail: [email protected]

The cruise on the river went from the centre of Dres- in 1893, the middle part of this steel bridge spans den (Elbterrassen) down to the Loschwitz bridge, almost 150 m without intermediate pylon – at that famous as the “Blue Miracle” (Blaues Wunder). Built time an amazing technical achievement. The colour

1 2 Figs 1-2. Portrait of Dr. O. Staudinger and title page of the “Catalog” (3rd ed., 1901).

240 ©Zoologische Staatssammlung München/Verlag Friedrich Pfeil; download www.pfeil-verlag.de was light blue. Connecting the formerly suburban areas of Loschwitz and Blasewitz, this bridge has, in a way, a historical relation to entomology: Dr. Otto Staudinger and Andreas Bang-Haas, the owners of the well-known firm Staudinger & Bang-Haas (cf. Figs 1-3) trading in Lepidoptera from remote and exciting parts especially of the palaearctic region, had their homes at Blasewitz-Dresden. Staudinger’s “Catalog der Lepidopteren des palaearctischen Faunengebietes” (3rd ed. together with Rebel, 1901) is known to most lepidopterists. The major part of the important Staudinger collection with many type specimens is housed at the Museum of the Humboldt University of Berlin. A part of Staudinger’s collection came, however, together with the collection of Bang-Haas, to the Museum in Dresden (Senckenberg Fig. 3 Advertisement of the firm Staudinger & Bang- Museum für Tierkunde) and was shown to the par- Haas, printed at the end of the book K. Lampert, Die ticipants of Forum Herbulot 8 by Matthias Nuss. Großschmetterlinge und ihre Raupen Mitteleuropas, Verlag J. F. Schreiber, Esslingen/München 1907.

Conference Materials Forum Herbulot 2014

Forum Herbulot 2014 statement on accelerated biodiversity assessment (Community Consensus Position)

Forum Herbulot

Forum Herbulot 2014. Forum Herbulot 2014 statement on accelerated biodiversity assessment (Community Consensus Posi- tion). Pp. 241-242 in: Hausmann, A. (ed.). Proceedings of the eighth Forum Herbulot 2014. How to accelerate the inventory of biodiversity (Schlettau, 30 June – 4 July 2014). Spixiana 37 (2). Axel Hausmann (corresponding author for Forum Herbulot), SNSB – ZSM, Bavarian State Collection of Zoology, Münch- hausenstr. 21, 81247 Munich, Germany; e-mail: [email protected]

Forum Herbulot is a research initiative, founded in To achieve this goal we urge national and interna- the year of 2000, with approx. 150 members from 42 tional funding agencies, as well as decision-makers to countries. Most are renowned experts in Lepido provide substantial support and financial resources pterology (with a main focus on the largest family, to projects involving sampling, DNA barcoding, and Geometridae). During the 8th congress of the Forum taxonomic research. WE NEED TO consider that Herbulot, held between June 30th and July 5th at the mankind is facing, within the next few years, its big- Nature Conservation Centre of the Ore Mountains gest environmental crisis ever, i. e. the definitive and in Schlettau, Germany, attendants joined a general irreversible loss of a considerable part of biodiversity discussion of the topic “How to accelerate the in- on earth. Species on Earth are disappearing at an ventory of biodiversity” and decided to publish the alarming rate and it will soon be too late to perform following declaration: research on (and subsequent conservation of) life’s most precious heritage: biodiversity. FH urgently (1) Forum Herbulot (FH) highlights that global asks national and international authorities to endorse biodiversity assessment needs to be accelerated, and support biodiversity research by adopting col- through lecting/exportation regulations in fact facilitating, – extensive sampling projects, especially in tropi- rather than obstructing, research on biodiversity, cal and subtropical regions where a large part along the lines of Article 8a of the Nagoya Protocol of Lepidopteran diversity remains undescribed, on Access and Benefit Sharing. – species descriptions and – interim-assessments and characterization of (2) FH highlights the need of formally described diversity (e. g. DNA Barcoding, collection ma- species within the universally adopted Linnean nagement, databasing) system, but also recognizes the urgent need to develop and integrate the use of interim DNA-

241 ©Zoologische Staatssammlung München/Verlag Friedrich Pfeil; download www.pfeil-verlag.de

based systems to characterize species. Such an – DNA barcoding of holotypes as best practice for interim system can be generated, for instance, all newly described species. by the use of DNA barcoding, and of automati- (4) FH recommends, for species descriptions, the cally assigned Barcode Index Numbers (BIN), in following minimum quality standards (in addi- the Barcode of Life Datasystems (BOLD). The- tion to the minimum requirements of the Code): refore we welcome: – information on wing pattern – the forthcoming online documentation of BIN – internal morphological features (usually genita- history in BOLD lia) – DNA barcoding programs focusing on unnamed – genetics (preferably the standard DNA barcode, species (suspected to be new) in collections i. e. the 5' 658 bp of the COI gene) if available – projects of DNA barcoding of type specimens. – differential diagnosis from the closest related National funding agencies and decision-makers species. FH encourages careful and thorough should commit themselves quickly to provide differential diagnoses, as well as full biblio- substantial support and financial resources to graphic references to the original descriptions generate DNA-barcodes for all type specimens of all mentioned species names in taxonomic deposited in their national collections. publications whenever possible. (3) FH acknowledges the advantages of modern (5) Common resource data: FH supports the Bou- tools for species descriptions, and supports/ chout Declaration (http://bouchoutdeclaration. encourages: org/) for open access to biodiversity data and – electronic publication of species descriptions thus strongly encourages opening for free use linked to online databases the online access to key biodiversity data inclu- – development of interfaces linking DNA barcode ding sequences (along with access numbers on data (e. g. BOLD), online publishing tools and BOLD and GenBank/EMBL/DDBJ published in other online databases (e. g. GenBank, GBIF, EOL, the original descriptions), taxonomic names, etc.) descriptions, occurrence data, images, ecological – registration in Zoobank as a standard for all new dates, habitats, biological traits and data. nomenclatural acts The Forum Herbulot, 3 July 2014, Schlettau (Germany)

Claude Herbulot – his way of accelerating biodiversity assessment

Axel Hausmann

Hausmann, A. 2014. Claude Herbulot – his way of accelerating biodiversity assessment. P. 242 in: Hausmann, A. (ed.). Proceed- ings of the eighth Forum Herbulot 2014. How to accelerate the inventory of biodiversity (Schlettau, 30 June – 4 July 2014). Spixiana 37 (2). Axel Hausmann, SNSB – ZSM, Bavarian State Collection of Zoology, Münchhausenstr. 21, 81247 Munich, Germany; e-mail: [email protected]

Claude Herbulot (1908-2006) published descriptions author of more than 300 geometrid species descrip- of close to 800 valid geometrid species. Only three tions and nowadays worldwide description rates taxonomists ever described more geometrid species dropped below 100 per year for this family. At this than him (Prout 3591 species, Warren 2282 species, pace, another 200 years may be needed for describ- Walker 1027 species). All of them used “short- ing the remainder of species. Forum Herbulot 2014 description-methods” that would not be accepted offers the scientific platform for discussing how by today’s peer-reviewed journals and reviewers. modern methods allow adjusting our standards and Current requirements and high standards for species description practice to achieve an acceleration of descriptions, as well as lacking funds for taxonomy biodiversity assessment. One of these tools is DNA lead to a deceleration of species description rates. barcoding which has provided genetic assessment So far, some 23 000 geometrid species have been for 20 000 geometrid species in just eight years. The described, but research on unidentified collection results of the discussions are published in the “Forum material and results from the global DNA barcoding Herbulot 2014 statement on accelerated biodiversity campaign suggest that there are more than 40 000 assessment”. species on earth. However, no living taxonomist is

242 ©Zoologische Staatssammlung München/Verlag Friedrich Pfeil; download www.pfeil-verlag.de

Taxonomy – faster. Better

Michael Balke

Balke, M. 2014. Taxonomy – faster. Better. P. 243 in: Hausmann, A. (ed.). Proceedings of the eighth Forum Herbulot 2014. How to accelerate the inventory of biodiversity (Schlettau, 30 June – 4 July 2014). Spixiana 37 (2). Michael Balke, SNSB – ZSM, Bavarian State Collection of Zoology, Münchhausenstr. 21, 81247 Munich, Germany; e-mail: mi- [email protected]

The term “turbo-taxonomy” was recently coined global biodiversity. While this approach is certainly for an approach combining cox1 sequences, concise not suitable for all taxa alike, it is the tool that will morphological descriptions by an expert taxonomist, help to tackle many hyper diverse groups and pave and high-resolution digital imaging to streamline the road for more sustainable comparative stud- the formal description of larger numbers of new ies. Finally, we will present a proposed large-scale species. We further developed this approach and pilot study in Indonesia, and argue that fast track demonstrate the functionality of a species-descrip- taxonomy and the BIN system will have to work tion pipeline by naming 101 new species of hyper hand in hand to provide objective, sustainable data diverse New Guinea Trigonopterus Fauvel, 1862 in such a large framework where it is hopeless to weevils in the open-access journal ZooKeys (Riedel assume that traditional tools will be able to inform et al. 2013). We conclude that fast track taxonomy stakeholders about the contents of a given area. will not only increase speed, but also sustainability of global species inventories. It will be of great practical Riedel, A., Sagata, K., Surbakti, S., Tänzler, R. & Balke, value to all the other disciplines that depend on a M. 2013. One hundred and one new species of usable taxonomy and will change our perception of Trigonopterus weevils from New Guinea. ZooKeys 280: 1. doi:10.3897/zookeys.280.3906

Global digital infrastructure for biological nomenclature and taxonomy

Ellinor Michel, Richard L. Pyle & Robert P. Guralnick

Michel, E., Pyle, R. L. & Guralnick, R. P. 2014. Global digital infrastructure for biological nomenclature and taxonomy. P. 243 in: Hausmann, A. (ed.). Proceedings of the eighth Forum Herbulot 2014. How to accelerate the inventory of biodiversity (Schlet- tau, 30 June – 4 July 2014). Spixiana 37 (2). Ellinor Michel (corresponding author), Department of Life Sciences, The Natural History Museum, London, UK; e-mail: [email protected]

The future for interoperable scientific information is nomenclatural registration system. Users are applied digital, yet scientific names, the handles for all bio- scientists in agriculture, medicine, veterinary science diversity information, remain without an integrated and climate change research; biodiversity researchers system tied to published descriptions and museum such as ecologists, physiologists; archives such as type specimens. Descriptions and type specimens museums; the scientific publishing community – in provide standards for the otherwise fluid concepts short, all users of scientific names of organisms based of biological taxa. We are working to unify the in- on the work of taxonomists. frastructures for biological nomenclature across nomenclatural codes (including zoological (ICZN 2014, ICNafp 2014. International Code of Nomenclature for http://iczn.org/), botanical (ICNafp 2014, http:// algae, fungi and plants. http://www.iapt-taxon. www.iapt-taxon.org/nomen/main.php/) and bac- org/nomen/main.php/ [accessed 06-Oct-2014] terial (ICNB) codes) through the Global Names ICZN 2014. International Commission on Zoological Architecture (GNA). Our initial focus is on animal Nomenclature. http://iczn.org/ [accessed 06-Oct- 2014] names, as these comprise the largest component of ZooBank 2014. The Official Registry of Zoological metazoan biodiversity and ZooBank (Zoobank 2014, Nomenclature. http://zoobank.org/ [accessed 06- http://zoobank.org/) is the first code-related online Oct-2014]

243 ©Zoologische Staatssammlung München/Verlag Friedrich Pfeil; download www.pfeil-verlag.de

Streamlining descriptions of new species identified with barcode data Lyubomir Penev & Pavel Stoev

Penev, L. & Stoev, P. 2014. Streamlining descriptions of new species identified with barcode data. P. 244 in: Hausmann, A. (ed.). Proceedings of the eighth Forum Herbulot 2014. How to accelerate the inventory of biodiversity (Schlettau, 30 June – 4 July 2014). Spixiana 37 (2). Lyubomir Penev (corresponding author), Pensoft Publishers, Prof. Georgi Zlatarski Street 12, 1700 Sofia, Bulgaria; e-mail: [email protected]

We offer a solution for streamlining of descriptions and Discussion and other sections to meet the stand- of new species among the “dark taxa” identified ards of a conventional scholarly publication and as such with barcode data by establishing a data then submitted for a community peer-review and export and publication workflow between BOLD publication in the Biodiversity Data Journal (BDJ). and Pensoft. Voucher specimens metadata (e. g. On the day of publication, BDJ will return back to occurrences, images, classifications, methodology BOLD – either through automated metadata export applied, etc.) that are deemed to represent new taxa or through a harvesting mechanism – all data and (e. g. their BIN numbers do not match a particular text of the published paper in machine-readable taxon concept) could be imported from BOLD into format, so that these could be linked back to the Pensoft’s Writing Tool (PWT) through PWT’s API original BOLD record. “at the click of a button”. In this way, the authors A similar workflow can be established also for will generate a taxonomic manuscript, comprising data papers describing large data sets. Data paper a number of taxon treatments with their structural manuscripts (also known as “barcode data release” elements being automatically filled in. papers) can be generated from the metadata descrip- Authors could then further elaborate the treat- tors at BOLD and submitted as almost finalized ments by providing specific epithets, concise mor- manuscripts into the data paper template of PWT phological description, diagnosis, type specification, and then to BDJ. or additional taxonomic remarks to complete the Analogous workflows but based on text file taxonomic description in a way to meet the require- submissions (e. g. RTF) can also be established with ments of the biological codes. The manuscript then ZooKeys and other journals. could be extended further with Introduction, Results

The BIN system: standardizing molecular operational taxonomy in animals Sujeevan Ratnasingham

Ratnasingham, S. 2014. The BIN system: standardizing molecular operational taxonomy in animals. P. 244 in: Hausmann, A. (ed.). Proceedings of the eighth Forum Herbulot 2014. How to accelerate the inventory of biodiversity (Schlettau, 30 June – 4 July 2014). Spixiana 37 (2). Sujeevan Ratnasingham, Biodiversity Institute of Ontario, University of Guelph, Guelph, ON, N1G 2W1, Canada; e-mail: [email protected]

The Barcode Index Number (BIN) system is an algo- barcode region of the cytochrome c oxidase I (COI) rithmic system that registers operational taxonomic gene. The algorithmic methods utilized are designed units (OTUs) based on DNA barcodes in the Barcode to restructure registered OTUs, merging in some of Life Data System. It has been designed and devel- cases and splitting in others, when new data sup- oped to address the large number of unrecognized ports it. Such dynamism, although challenging at animal species on the planet. By assigning indi- times to work with, reflects conventional taxonomic viduals to presumptive species this system speeds processes, is necessary to accurately illuminate dark investigations into the patterning of biodiversity taxa. Aside from a pragmatic role in biodiversity and enable studies that would otherwise be impos- assessments, BINs aid revisionary taxonomy by sible. Although OTUs have conventionally been flagging possible cases of synonymy, and by collat- separated through their morphological divergence, ing geographical information, descriptive metadata, DNA-based delineations have important advantages. and images for specimens that are likely to belong OTU designation can be automated, data can be to the same species, even if it is undescribed. With readily archived, and results can be easily compared over 300 000 registered OTUs and associated web among investigations. The BIN system exploits these pages now available, the BIN system continues to attributes and provides a persistent, species-level evolve with new functionality including detailed taxonomic registry for the animal kingdom based on audit trails and community annotations. the analysis of patterns of nucleotide variation in the

244 ©Zoologische Staatssammlung München/Verlag Friedrich Pfeil; download www.pfeil-verlag.de

From BINs to biodiversity: rapid arthropod assessments using DNA barcodes

Jeremy deWaard, Claudia Bertrand, Kara Layton, Angela Telfer & Monica Young

deWaard, J., Bertrand, C., Layton, K., Telfer, A. & Young, M. 2014. From BINs to biodiversity: rapid arthropod assessments using DNA barcodes. P. 245 in: Hausmann, A. (ed.). Proceedings of the eighth Forum Herbulot 2014. How to accelerate the inventory of biodiversity (Schlettau, 30 June – 4 July 2014). Spixiana 37 (2). Jeremy deWaard (corresponding author), Bio-Inventory and Collections, Biodiversity Institute of Ontario, University of Guelph, ON, N1G 2W1, Canada; e-mail: jeremy.dewaardj@ uoguelph.ca

The vast majority of animal species in terrestrial project is currently running in its third year, and ecosystems are arthropods, yet contemporary envi- has completed analysis for the first year of field ronmental assessments all but ignore this massive collection. In 2012, 14 sites and 189 weekly malaise assemblage, and its susceptibility to disturbance samples were processed, to reveal nearly 150 000 is unmeasured. We address this shortfall through specimens, and over 15 000 distinct Barcode Index a time- and cost-efficient approach for terrestrial Numbers (BINs), a reliable proxy for species. Another arthropod assessments based on DNA barcode effective application of this approach involves the analysis of specimens collected by Malaise traps. early detection of non-indigenous species (NIS) at In a study we conducted in 2012 comparing sev- Canada’s ports. The Halifax Port project has analysed eral standardized techniques, Malaise traps were 20 weekly samples from a single Malaise trap in the found to be the most efficient sampling method vicinity of the port, and revealed several potential in terms of capturing the largest proportion of the and known NIS, including the recently discovered arthropod assemblage with minimal effort. The beech flea weevil (Orchestes fagi (Linnaeus, 1758)). In material collected by Malaise traps are currently the near future, this approach will require a shift to individually sorted, analyzed in a 384-well pipeline, Next Generation Sequencing (NGS) to facilitate time- and Sanger-sequenced; this approach permits the and cost-efficient sequencing of bulk samples. Initial link between each barcode record and its source NGS trial runs have resulted in high BIN recovery specimen to be maintained, and facilitates the con- for bulk samples (> 95 %), but some analytical biases struction of a barcode reference library based on (such as amplification and body mass bias) require carefully identified specimens. The assignment of further fine-tuning of protocols. The integration of taxonomy following analysis is achieved through NGS analyses with DNA barcode reference libraries matches with authoritatively identified records on could ultimately set the global standard for rapid Barcode of Life Data Systems (BOLD 2014, http// biodiversity assessment, one that finally includes www.boldsystems.org/) and by collaborating with the terrestrial arthropod component. taxonomic specialists. This approach is currently employed in several ongoing studies, including a BOLD 2014. Barcode of Life Data Systems. http//www. multi-year project inventorying arthropods in all boldsystems.org/ [accessed 06-Oct-2014] of Canada’s 45 National Parks (CNP). The CNP

DNA barcode enabled ecological research on Geometridae in Papua New Guinea

Scott E. Miller

Miller, S. E. 2014. DNA barcode enabled ecological research on Geometridae in Papua New Guinea. Pp. 245-246 in: Hausmann, A. (ed.). Proceedings of the eighth Forum Herbulot 2014. How to accelerate the inventory of biodiversity (Schlettau, 30 June – 4 July 2014). Spixiana 37 (2). Scott E. Miller, National Museum of Natural History, Smithsonian Institution, Washington, DC 20013, USA; and Binatang Research Centre, Box 604, Madang, Papua New Guinea; e-mail: [email protected]

DNA barcoding of the Geometridae of Papua New terization of the insects reared from woody plants, Guinea provides a framework for multiple lines but we are increasingly combining those data with of systematic and ecological research, as part of a bioassessments of adults using light traps (Pagi et large-scale study of insect-plant ecology and bio- al. in preparation). DNA barcoding provides a rapid geography in forests in Papua New Guinea by the and accurate taxonomic framework, which is also Binatang Research Centre (Novotny et al. 2010). instrumental in analysis of phylogeographic patterns The foundation of the program has been charac- (Craft et al. 2010), identifying caterpillars (Miller

245 ©Zoologische Staatssammlung München/Verlag Friedrich Pfeil; download www.pfeil-verlag.de et al. 2013), detecting host-parasitoid interactions Holloway, J. D., Miller, S. E., Pollock, D. M., Helgen, L. (Hrcek et al. 2013), linking historic types with modern & Darrow, K. 2009. GONGED (Geometridae of New specimens (Holloway et al. 2008), identifying host Guinea Electronic Database): a progress report on plants from caterpillar stomach contents (Erickson development of an online facility of images. Spixi- et al. in preparation), and phylogeny (Segar et al. ana 32: 122-123. Hrcek, J., Miller, S. E., Whitfield, J. B., Shima, H. & Novo- in preparation, including additional genes). DNA tny, V. 2013. Parasitism rate, parasitoid community barcodes add great value to the taxonomic and eco- composition and host specificity on exposed and logical data, making them useful to a broad range semi-concealed caterpillars from a tropical rainfor- of research enterprises, and allowing linkage with est. Oecologia 173: 521-532. other projects, especially through the BIN system Miller, S. E., Hrcek, J., Novotny, V., Weiblen, G. D. & (Ratnasingham & Hebert 2013). Hebert, P. D. N. 2013. DNA barcodes of caterpillars This work is highly collaborative, and has been (Lepidoptera) from Papua New Guinea. Proceed- supported by the USA and Czech National Science ings of the Entomological Society of Washington Foundations, USA National Institutes of Health, 115: 107-109. Moore Foundation, Genome Canada, Natural His- Novotny, V., Miller, S. E., Baje, L., Balagawi, S., Basset, tory Museum (London), Biodiversity Institute of On- Y., Cizek, L., Craft, K. J., Dem, F., Drew, R. A. I., Hulcr, J., Leps, J., Lewis, O. T., Pokon, R., Stewart, tario, PNG National Agriculture Research Institute, A. J. A., Samuelson, G. A. & Weiblen, G. D. 2010. University of Minnesota, and many other funders Guild-specific patterns of species richness and host and collaborators. specialization in plant–herbivore food webs from a tropical forest. Journal of Animal Ecology 79: Craft, K. J., Pauls, S. U., Darrow, K., Miller, S. E. Hebert, 1193-1203. P. D. N., Helgen, L. E. Novotny, V. & Weiblen, G. D. Ratnasingham, S. & Hebert, P. D. N. 2013. A DNA-based 2010. Population genetics of ecological communities registry for all animal species: the Barcode Index with DNA barcodes: an example from New Guinea Number (BIN) system. PloS ONE 8(7): e66213. Lepidoptera. Proceedings of the National Academy of Science USA 107: 5041-5046.

Accelerating the inventory of Lepidoptera early stages and host-plant and other associations by using citizen science projects

Hermann S. Staude

Staude, H. S. 2014. Accelerating the inventory of Lepidoptera early stages and host-plant and other associations by using citizen science projects. P. 246 in: Hausmann, A. (ed.). Proceedings of the eighth Forum Herbulot 2014. How to accelerate the inventory of biodiversity (Schlettau, 30 June – 4 July 2014). Spixiana 37 (2). Hermann S. Staude, Magaliesburg, South Africa; e-mail: [email protected]

The ability to identify the early stages of Lepidoptera the early stages of our Lepidoptera by exploiting and knowledge of their host-plant preferences is this growing enthusiasm in the natural history of of fundamental importance in understanding their smaller creatures. ecological interactions, biogeography and potential This presentation reported on the creation of a economic impact. In South Africa the early stages citizen science project aimed at visually recording (or any part thereof) and host-plant associations the “caterpillar – host-plant – adult” associations of are known for less than 10 % of the Lepidoptera African Lepidoptera, which culminated in the for- fauna estimated to be over 10 000 species. Images mation of the now active Caterpillar Rearing Group or illustrations of these early stages are available for under the auspices of The Lepidopterists’ Society of only a fraction of the species for which at least some Africa. information is available. The advent of modern com- In the first eighteen months the project has munication media such as nature websites, online yielded some spectacular results: Number of valid databases, Virtual Museums and social media, as entries received: 1168. Number of species for which well as the free availability of good digital cameras, we now have the minimum criteria: 725. Number of has sparked a renewed interest in the smaller fauna host-plant associations new to science: 568. Minimum by the South African public. This prompted us to number of species never reared before: 214. find ways of rapidly accelerating the discovery of

246 ©Zoologische Staatssammlung München/Verlag Friedrich Pfeil; download www.pfeil-verlag.de

DNA barcoding and DNA metabarcoding as tools for rapid inventory and high-throughput identification of Lepidoptera species in Amazonia

Rodolphe Rougerie, Thibaud Decaëns, David C. Lees, Carlos Lopez-Vaamonde, Shadi Shokrala & Mehrdad Hajibabaei

Rougerie, R., Decaëns, T., Lees, D. C., Lopez-Vaamonde, C., Shokrala, S. & Hajibabaei, M. 2014. DNA barcoding and DNA metabarcoding as tools for rapid inventory and high-throughput identification of Lepidoptera species in Amazonia. P. 247 in: Hausmann, A. (ed.). Proceedings of the eighth Forum Herbulot 2014. How to accelerate the inventory of biodiversity (Schlettau, 30 June – 4 July 2014). Spixiana 37 (2). Rodolphe Rougerie (corresponding author), INRA Orléans, France; e-mail: [email protected]

In the fields of ecology and conservation biology, possible as well as a large portion of unidentified when information requiring species-level identifi- species only characterized to date by their Barcode cation is needed, many groups of living organisms Index Number (BIN) in BOLD. are generally excluded de facto from the studies, As an alternative approach and to demonstrate merely because of the lack of access to the scarce the usefulness of DNA barcode libraries, we car- specific taxonomic expertise and because of the ried out a community ecology study in Brazilian largely unexplored and overwhelming diversity and Colombian Amazonia where we used a DNA of some taxa, in particular in the species-rich inter- metabarcoding approach to identify bulk samples tropical regions. In French Guiana, we used standard of Saturniidae and Sphingidae moths along a gradi- Sanger-based DNA barcoding to document this ent of land-uses. This study used Next Generation relatively unknown tropical lepidopteran fauna, Sequencing technology (454 Roche) to expedite the revealing an outstanding local diversity. Our efforts process of sequencing a large number of samples resulted in the assembly of a large DNA barcode (ca. 1700) in many collecting sites (54). library comprising expert-identified species when

The flowchart of taxonomy – right pieces in the right order

Mari Kekkonen

Kekkonen, M. 2014. The flowchart of taxonomy – right pieces in the right order. Pp. 247-248 in: Hausmann, A. (ed.). Proceed- ings of the eighth Forum Herbulot 2014. How to accelerate the inventory of biodiversity (Schlettau, 30 June – 4 July 2014). Spixiana 37 (2). Mari Kekkonen, Finnish Museum of Natural History, Zoology Unit, University of Helsinki, P.O. Box 17, 00014, Helsinki, Finland; e-mail: [email protected]

Challenge trophinae (Kekkonen 2014). The flowchart includes four steps, starting from the phylogenetic analyses Numerous insect groups include a great amount of concentrating on the hierarchical level above the unknown species, and many of them lack present- focal group (for further details, see Heikkilä et al. day taxonomic expert. One such group is the Austral- 2014). The next phase introduces DNA barcode- ian Hypertrophinae (Gelechioidea: Depressariidae) based delineation of putative species (i. e. operational with 51 described and tens of undescribed species. taxonomic units, OTUs) (for further details, see Kek- Very little is known about these endemic moths, konen & Hebert 2014), and the third part returns to mainly due to their insufficient taxonomy. To be the phylogenetics, but this time, at the level of the able to gather knowledge on hypertrophines, their focal group. The last step includes the validation of species boundaries need to be defined, phylogenetic OTUs based on all available data (e. g. morphological relationships studied, and newly discovered species characters, nuclear loci), and subsequent association described. However, their small size, somewhat of type specimens with defined species by applying cryptic wing patterns, and the lack of present-day DNA barcodes. experts pose a considerable challenge. Reason Solution A rationale behind the flowchart of taxonomy is to A flowchart of taxonomy was recently presented to choose the most suitable source of data and the set describe the workflow of the study of the Hyper- of methods for each phase. The flowchart presents

247 ©Zoologische Staatssammlung München/Verlag Friedrich Pfeil; download www.pfeil-verlag.de a viewpoint where initial boundaries of putative Heikkilä, M., Mutanen, M., Kekkonen, M. & Kaila, L. species are formed based on DNA barcodes. This 2014. Morphology reinforces proposed molecular approach offers many benefits when compared to phylogenetic affinities: a revised classification for generally used “morpho grouping”. As initial species Gelechioidea (Lepidoptera). Cladistics 30 (6): 563- delineation forms a distinct phase with one source of 589. http://dx.doi.org/10.1111/cla.12064 Kekkonen, M. 2014. Taxon delineation in gelechioid data and is based on specified delineation methods, moths: from phylogenetics to DNA barcoding. 60 it is repeatable and more objective. Furthermore, pp., PhD thesis, University of Helsinki. http://urn. with a group including tens of unknown species, fi/URN:ISBN:978-952-10-9895-6 the total duration of taxonomic work is considerably – – & Hebert, P. D. N. 2014. DNA barcode-based deline- shorter and the taxonomic accuracy is improved as ation of putative species: efficient start for taxonom- many cryptic species are discovered in the begin- ic workflows. Molecular Ecology Resources 14: 706- ning. Although single-locus mtDNA poses possible 715. http://dx.doi.org/10.1111/1755-0998.12233 problems especially with recently diverged species, these drawbacks will most likely be revealed in the validation phase.

With or without speed-limit? How to assess 3000 Emerald species (Lepidoptera, Geometridae, Geometrinae)

Axel Hausmann, Hermann S. Staude, Clarissa Dieterle & Alfred Moser

Hausmann, A., Staude, H. S., Dieterle, C. & Moser, A. 2014. With or without speed-limit? How to assess 3000 Emerald species (Lepidoptera, Geometridae, Geometrinae). P. 248 in: Hausmann, A. (ed.). Proceedings of the eighth Forum Herbulot 2014. How to accelerate the inventory of biodiversity (Schlettau, 30 June – 4 July 2014). Spixiana 37 (2). Axel Hausmann, SNSB – ZSM, Bavarian State Collection of Zoology, Münchhausenstr. 21, 81247 Munich, Germany; e-mail: [email protected]

So far, 2225 Emerald species (subfamily Geometri- revision of the African species of the genera Pingasa nae) have been described worldwide. Based on the Moore, 1887, Prasinocyma Warren, 1897 and Victoria material studied in various collections and on the ac- Warren, 1897, and the Neotropical species of the cumulation curve of DNA Barcode clusters (Barcode genera Lophochorista Warren, 1904, Oospila Warren, Index Numbers, “BIN”s, cf. Ratnasingham & Hebert 1897, Nemoria Hübner, 1818 and Lissochlora Warren, 2013) in the international Barcode of Life project we 1900. The Natural History Museums of Munich, Lon- estimate the total species number to exceed 3000 spe- don and Pretoria (ZSM, NHM, NFI; “Afroemeralds cies. We studied the material from major collecting Project”) initiated an integrated assessment of all type projects in the Neotropical and Afrotropical regions, specimens of Geometrinae including DNA barcod- e.g. in Ethiopia, Tanzania, South Africa, Ghana, ing, genitalia dissection, digital photography and Cameroun, Mali, Brazil, Peru, Ecuador, Colombia accurate databasing to rapidly achieve an objective, and Costa Rica. Our integrative taxonomic approach close-to-complete knowledge of the Geometrinae combines information from DNA barcoding with fauna of the whole African continent. Furthermore, classical morphological methods. Preliminary results representatives of all BIN-clusters on the barcode of and accumulation curves suggest the total species Life Datasystems (BOLD) are submitted to genitalia number of the subfamily Geometrinae to increase dissection. from 458 to more than 750 in the Neotropical region (currently available: 2450 DNA barcodes clustering to Ratnasingham, S. & Hebert, P. D. N. 2013. A DNA-based 557 BINs) and from 633 to more than 1000 in Africa registry for all animal species: the Barcode Index (currently available: 2510 DNA barcodes clustering to Number (BIN) system. PLoS ONE 8(7): e66213. 676 BINs). The first research focus was laid on the the doi:10.1371/journal.pone.0066213

248 ©Zoologische Staatssammlung München/Verlag Friedrich Pfeil; download www.pfeil-verlag.de

DNA barcoding reveals that the reverse latitudinal gradient of Gracillariidae leaf-miners is an artefact of tropical under-sampling

Carlos Lopez-Vaamonde, David C. Lees, Akito Kawahara, Rodolphe Rougerie, Issei Ohshima, Atsushi Kawakita, Olivier Bouteleux & Jurate De Prins

Lopez-Vaamonde, C., Lees, D. C., Kawahara, A., Rougerie, R., Ohshima, I., Kawakita, A., Bouteleux O. & De Prins, J. 2014. DNA barcoding reveals that the reverse latitudinal gradient of Gracillariidae leaf-miners is an artifact of tropical under-sampling. P. 249 in: Hausmann, A. (ed.). Proceedings of the eighth Forum Herbulot 2014. How to accelerate the inventory of biodiversity (Schlettau, 30 June – 4 July 2014). Spixiana 37 (2). Carlos Lopez-Vaamonde (corresponding author), INRA-Orléans, UR633, Unité de Zoologie, Orléans, France; e-mail: carlos. [email protected]

With thousands of undescribed tropical Lepidoptera was estimated after comparison with types. The species and alarming rates of deforestation, develop- total number of candidate species ranged from 142 ing methods that allow rapid biodiversity assessment (ABGD) to 151 (BINs). For Nouragues we obtained is crucial to quantify levels of endemism and identify 108 BINs. 64 BINs (59.3 %) are represented by sin- areas of high conservation value. DNA barcoding has gletons. 33 % of specimens were identified down to been shown to be an efficient tool to speed up the genus level. We were able to assign 17 species names identification of known species and the discovery of to 38 specimens. Strikingly, at least 85 % of the species new ones. Barcodes can be used as proxy for cluster- collected as adults were found to be undescribed. ing unidentified specimens into operational units Nearly all barcodes were novel to BOLD. The re- and estimate levels of diversity within and between sults from both our molecular and morphological sites. This approach can be used to carry out rapid analyses indicate that most of the gracillariid fauna biodiversity assessments of hyperdiverse, mostly in the studied region is unknown and undescribed. undescribed, insect fauna in tropical areas. Here we The estimated lower bound of species richness of use DNA barcode data to quantify species richness Gracillariidae for Nouragues ranged from 240 species of Gracillariidae leaf-mining moths of several sites (Chao1) to 260 species (ACE). Our results show that in French Guiana and Ecuador. DNA barcoding allows researchers to overcome the Field surveys in six French Guianan (Fig. 1) taxonomic impediment and carry out rapid biodi- and one Ecuadorian sites produced 516 gracillariid versity assessments in poorly documented regions specimens that were DNA barcoded to facilitate iden- (Lees et al 2013). tification and to match larvae inside leaf-mines with adults. We obtained 485 barcodes (372 adults and Lees, D. C., Kawahara, A. Y., Rougerie, R., Ohshima, 104 larvae). Species delineation from sequence data I., Kawakita, A., Bouteleux, O., De Prins, J. & was approximated using Automatic-Barcode-Gap- Lopez-Vaamonde, C. 2013. DNA barcoding reveals Discovery and Refined-Single-Linkage-Analysis a largely unknown fauna of Gracillariidae leaf- through the Barcode Index Number system, and mining moths in the Neotropics. Molecular Ecology Resources 14 (2): 286-296. the proportion of described/undescribed species

Using DNA barcoding as a tool to describe moth community patterns in Lopé and Ivindo National Parks, Gabon

Sylvain Delabye, Thibaud Decaëns, Sandrine Bayendi, Stephan Ntie, Philippe Le Gall, Carlos Lopez Vaamonde, Nicolas Moulin, David Sebag, Rodolphe Rougerie & the Ecotrop team

Delabye, S., Decaëns, T., Bayendi, S., Ntie, S., Le Gall, P., Lopez Vaamonde, C., Moulin, N., Sebag, D., Rougerie, R. & the Ecotrop team. 2014. Using DNA barcoding as a tool to describe moth community patterns in Lopé and Ivindo National Parks, Gabon. Pp. 249-250 in: Hausmann, A. (ed.). Proceedings of the eighth Forum Herbulot 2014. How to accelerate the inventory of biodiversity (Schlettau, 30 June – 4 July 2014). Spixiana 37 (2). Sylvain Delabye (corresponding author), Université Rouen, France; e-mail: [email protected]

The existence of a taxonomic shortfall has been where natural communities are more diverse and stressed as an important constraint for invertebrate less studied. Here, we used DNA barcoding to biodiversity studies, especially in tropical countries achieve a rapid description of moth communities

249 ©Zoologische Staatssammlung München/Verlag Friedrich Pfeil; download www.pfeil-verlag.de in two contrasted ecosystems of central Gabon: the but richness estimators indicate that up to 1700 and rainforest of Ipassa research station (November 1440 species could occur in both sites. Accordingly, 2009), and the savannah/forest patchwork near sampling coverage ranged from 65 to 75 % (in Ipassa La Lopé (November 2009, March 2011). Specimens and La Lopé, respectively). When comparing com- collected at light-trap were subsequently sorted by position among sites (2009 dataset), we found a 66 % morphospecies, of which up to four individuals were BINs turnover, suggesting a strong spatial structur- selected and processed through DNA barcoding. ing due to geographical distance and/or contrasted The diversity and composition of the communities environmental conditions. Likewise, turnover was are described using Barcode Index Numbers (BINs) of 68 % between two sampling periods in La Lopé, as operational taxonomic units considered here as indicating that communities could also be strongly proxy for species. Family-level assignment was car- structured according to seasonal cycle. ried out using morphology and/or existing DNA This study represents a first step in the descrip- barcode libraries in BOLD (BOLD 2014, http//www. tion of moth diversity in ecosystems of Gabon. In boldsystems.org/). 2012, 2013 and 2014, sampling was intensified by A total of 3307 DNA barcodes were obtained from involving students of the ECOTROP field school and the 3387 specimens collected, representing 1305 BINs by diversifying collecting methods. A total of 3000 and 22 families, of which the most represented are additional individuals were sampled and their DNA Noctuidae, Erebidae and Geometridae. We found barcodes will be sequenced in the next few months, 733 singletons (i. e. 56 % of the total BINs number), which hopefully will strengthen and refine the de- suggesting a high proportion of rare species in scription of community patterns in Lopé National communities and/or a significant level of under- Park. sampling, which is a classical limit in most tropical arthropod surveys. Observed richness was of 807 BOLD 2014. Barcode of Life Data Systems. http//www. and 713 BINs in Ipassa and La Lopé, respectively, boldsystems.org/ [accessed 06-Oct-2014]

The importance of the traditional taxonomy in the exploration of the real biodiversity of Lepidoptera. A study case: the Nolini (Lepidoptera, Nolinae, Noctuoidea) fauna of Eurasia

Gyula M. László, Gabor Ronkay & László Ronkay

László, G. M., Ronkay, G. & Ronkay, L. 2014. The importance of the traditional taxonomy in the exploration of the real biodiversity of Lepidoptera. A study case: the Nolini (Lepidoptera, Nolinae, Noctuoidea) fauna of Eurasia. Pp. 250-251 in: Hausmann, A. (ed.). Proceedings of the eighth Forum Herbulot 2014. How to accelerate the inventory of biodiversity (Schlettau, 30 June – 4 July 2014). Spixiana 37 (2). Gyula M. László (corresponding author), Fadrusz u. 25, 1114 Budapest, Hungary; e-mail: [email protected]

After more than 200 years of the birth of the descrip- the discovery of an unexpectedly large number of tive science taxonomy, the exploration of the real new taxa. biodiversity of Lepidoptera is still far not complete. The history of the descriptions of Nolini species The ratio of the undiscovered taxa strongly depends is demonstrated in Figure 1. on the popularity of the given Lepidoptera group: The big leap in the number of new species de- usually the larger, spectacular groups are better ex- scribed in the last 14 years, thanks above all to Dr. J. plored than the small, less conspicuous ones, there Holloway (Natural History Museum, London) and are, however, several new discoveries even in the the present research group, is due to the increase of most popular groups. the available material from less explored areas and Our research team started the taxonomic work the thorough morpho-taxonomic studies. In many on the rather neglected Noctuoidea tribe Nolini groups of Nolini, according to the new results, a (Nolidae) in 2002, in collaboration with Mr. T. J. Witt number of (sometimes 4-5) externally undistinguish- and the Museum Witt, Munich, based on recently able species may occur sympatrically in a given area collected material from the Himalayas, Indochina, (the best example is the genus Manoba Walker, 1864), the Philippines and the Indonesian Archipelago. which can be properly separated and identified only After the detailed examination of all historical No- by the careful examination of the morphological lini types preserved in large European museums, structures of their genitalia. The study of the relevant we could continue the work on the vast material specific (distinctive) characters of the externally very harboured in these institutions that has resulted in similar species often requires a careful preparation

250 ©Zoologische Staatssammlung München/Verlag Friedrich Pfeil; download www.pfeil-verlag.de

technique and a coherent mounting process. This 300 267 work is often difficult and time-consuming due to 250 the small size of the animals. The steep rising tendency of the last decades 200 predicts a continuation of further discoveries and 150 descriptions of numerous new taxa, especially from 100 83 the hot spots of South East Asia and the Indonesian 48 32 39 36 Archipelago. Actually, the known Nolini fauna of 50 18 5 1 2 Eurasia has been doubled in the last fifteen years and 0 0 5 0 5 0 5 0 5 0 4 the case is similar for the African Nolini (Hacker et 0 2 5 7 0 2 5 7 0 1 8 8 8 8 9 9 9 9 0 0 1 1 1 1 1 1 1 1 2 2 al 2012). Such results may demonstrate the predic- 8- 1- 6- 1- 6- 1- 6- 1- 6- 1- 5 0 2 5 7 0 2 5 7 0 7 8 8 8 8 9 9 9 9 0 tions for the rate of the known/unknown species 1 1 1 1 1 1 1 1 1 2 of the recent fauna and insist the re-thinking of its Fig. 1. Numbers of valid taxa (species and subspecies) consequences. having been described since 1758. The Lepidoptera taxonomists and morphotax- onomy in the 21st century still have a decisive role in stock of information, otherwise they will be out of the exploration of the real biodiversity of the Earth. date already in the moment of their birth. This is Without getting at least close to the complete knowl- our responsibility and taxonomists still have a lot edge of the fauna of a given region or the species of things to do in order to accelerate our activity in content of a taxonomic unit it is simply too early to a highly co-operative manner, because the increas- establish ecological, biogeographical, phylogenetic ing destruction of the habitats of insects all over the etc. statements and conclusions on the, in fact poorly world will give us less and less opportunity to get known, subjects of the investigations. Our sample acquainted the real biodiversity of Planet Earth. case for the Nolini could be applicable for a number of other groups of Lepidoptera. Thus, for instance, all Hacker, H. H., Schreier, H-P. & Goater, B. 2012. Revision digital databasing projects must consider the newest of the tribe Nolini of Africa and the Western Palae- taxonomical revisions and follow the increase of the arctic Region (Lepidoptera, Noctuoidea, Noctuidae, described fauna instead of using the 20-50 years old Nolinae). Esperiana 17: 1-614.

Land in sight? – exploring the global geometrid diversity hotspot

Gunnar Brehm

Brehm, G. 2014. Land in sight? – exploring the global geometrid diversity hotspot. P. 251 in: Hausmann, A. (ed.). Proceedings of the eighth Forum Herbulot 2014. How to accelerate the inventory of biodiversity (Schlettau, 30 June – 4 July 2014). Spixiana 37 (2). Gunnar Brehm, Universität Jena, Germany; e-mail: [email protected]

The tropical Andes are known as the global diversity and assemblages become phylogenetically more hotspot of geometrid moths. Diversity has been in- clustered at higher elevations. Recent sampling and vestigated along a forested elevational gradient (ca. systematic barcoding reveals that species richness in 1000-3000 m) in south-eastern Ecuador since 1999. the area is much higher than previously thought and Surprisingly, diversity is constantly very high at microhabitats play an important role. Biodiversity in all elevations. There is a constant species turnover, the area is endangered by ongoing extensive forest subfamily composition changes with elevation, destruction.

Spatial and temporal pattern of species richness and abundance of macromoths including Geometridae in Mt. Jirisan National Park, South Korea

Sei-Woong Choi & Jeong-Seop An

Choi, S.-W. & An, J.-S. 2014. Spatial and temporal pattern of species richness and abundance of macromoths including Geo metridae in Mt. Jirisan National Park, South Korea. Pp. 251-252 in: Hausmann, A. (ed.). Proceedings of the eighth Forum Herbu- lot 2014. How to accelerate the inventory of biodiversity (Schlettau, 30 June – 4 July 2014). Spixiana 37 (2).

251 ©Zoologische Staatssammlung München/Verlag Friedrich Pfeil; download www.pfeil-verlag.de

Sei-Woong Choi (corresponding author), Department of Environmental Education, Mokpo National University, Muan, Jeonnam 534-729, South Korea; National Institute of Ecology, Seocheon, Chungnam 325-813, South Korea; e-mail: [email protected]

We sampled macromoths from 2005 to 2013 at eleven studies: Geometridae was the most species-rich tax- sites in Mt. Jirisan National Park (JNP), the oldest and on, followed by Noctuidae, Erebidae, Notodontidae, largest national park in South Korea, to address the Drepanidae, and Sphingidae. Yearly change of spe- following questions: (1) what is the total macromoth cies richness and abundance of all macromoths was species richness of JNP and can the total moth spe- 502 species (± 68.34) and 5161 individuals (± 1349.9). cies richness be estimated after 9 years? (2) What is Yearly change of species richness and abundance the proportion of moth families and is this pattern of Geometrid moths was 173 species (± 20.17) and of family dominance similar to that seen in other 2328 individuals (± 772.9). Overall species richness areas? (3) What are the yearly patterns of macromoth and abundance for all macromoths and geometrids and geometrid species richness and abundances? In were similar, but the elevational pattern of geometrid total, 46 452 individuals belonging to 1185 species of species richness was different from the total species 21 families of macrolepidoptera were collected. The richness. Species richness and abundance of four proportions of dominant families were similar to dominant subfamilies of the Geometridae declined those reported in temperate and tropical moth fauna as elevation increased.

Current Research on Australian Geometridae – redefining the Tasmanian “Archiearinae” and the blitzing of Australia’s remote fauna

Catherine Byrne & Abbey Throssell

Byrne, C. & Throssell, A. 2014. Current research on Australian Geometridae – redefining the Tasmanian “Archiearinae” and the blitzing of Australia’s remote fauna. Pp. 252-254 in: Hausmann, A. (ed.). Proceedings of the eighth Forum Herbulot 2014. How to accelerate the inventory of biodiversity (Schlettau, 30 June – 4 July 2014). Spixiana 37 (2). Catherine Byrne (corresponding author), Tasmanian Museum and Art Gallery, Hobart, Tasmania, Australia; e-mail: [email protected]

Two areas of research on the Australian Geometridae to these moths being treated under the Archiearinae are reported in this presentation. Firstly we highlight are most likely convergent adaptations to a cold recent work on the Tasmanian representatives of environment and similar biology. All are diurnal the Archiearinae, which describes and discusses for geometrids with rather stout, highly melanised, hairy the first time all life cycle stages of all species, their bodies, relatively small eyes and brightly coloured biology and clarifies the phylogenetic position of hindwings in most species. These adaptations are these enigmatic taxa. Secondly the principal author a recurring theme in alpine moths. It is probable, presents findings on Australian Geometridae col- therefore, that Acalyphes Turner, 1926 and Dirce lected in six surveys of Australian flora and fauna Prout, 1910 (cf. Fig. 1) have been misplaced into the in remote areas of Australia. Archiearinae. These genera are most likely ennomine The Archiearinae have traditionally been consid- with close links to the Australian Nacophorini from ered a basally derived sub-family in the Geometri- the molecular and morphological evidence (Young dae. This phylogenetic position and the monophyly 2006, 2008). of the group have been contradicted recently on Several morphological characters have been used morphological (Young 2006, 2008) and molecular to corroborate a primitive phylogenetic position for studies (Young 2006, Yamomota & Sota 2007, Re- the Archiearinae. Unlike most geometrids, Holarctic gier et al. (2009), Mutanen et al. (2010), Sihvonen archiearines lack an accessory tympanum and have et al. 2011). The Tasmanian representatives of the a very narrow fenestra media (Minet 1983). Pupal amphipolar Archiearinae consist of five species and characters, have also been used to substantiate a two undescribed species of the genera Acalyphes basally derived status for Archiearis. This is discussed Turner and Dirce L. B. Prout. Young (2006) found comprehensively in Young (2006) The combination of that the superficial similarities of these taxa with the unusual features, diurnal habit, absence of secondary world fauna, the Holarctic Archiearis Hübner, 1823, tympanum and pupal autapomorphies may indicate Boudinotiana Leraut 2002, Palaearctic Leucobrephos that the Holarctic archiearines, rather than being a Grote, 1874 fauna and the Neotropical Lachnocephala sister group to the Geometridae is a derived group Fletcher, 1953 and Archiearides Fletcher, 1953 that led within the family. This is certainly supported by

252 ©Zoologische Staatssammlung München/Verlag Friedrich Pfeil; download www.pfeil-verlag.de molecular evidence (Young 2006, Yamomota & Sota 2007, Sihvonen et al. 2011). Recent research on the iconic Tasmanian alpine genera Acalyphes and Dirce clarifies the phylogenetic position and nomenclature of these Tasmanian endemics, describes comprehensively all stages of the life-cycle and provides previously unpublished information on their biology, ecology and distribution. Eggs, larvae and adults are all illustrated. Bush Blitz is a national species discovery project funded by the Federal Department of Sustainability, Environment, Water, Population and Communities with support from corporate sponsors. The main aims of this project are the collection of new species and the surveying of remote areas in Australia that are poorly known for their biodiversity. Australia Fig. 1. Larva of Dirce solaris on Epacris serpyllifolia with reduced number of prolegs (photo: Peter Robinson, has a rich geometrid fauna of around 1300 known TMAG). species with at least one third of the fauna still new or undescribed. The southern Australian geometrid fauna is highly endemic and entire groups such as 2) WA Sept. 2011 – Credo Reserve, Eastern Gold- the Oenochrominae s. str. are mainly only found in fields Australia. Much is yet to be learned about the biol- 20 new or undescribed species of geometrids in ogy of the Australian Geometridae. The Bush Blitz 18 genera were collected, including three in the surveys have enriched our knowledge of the Austral- Oenochrominae that were most likely new to ian Geometridae by adding new species, rare species science: and new records to our state museum collections and One male specimen only of an extremely rare spe- to the Atlas of Living Australia (2014, http://www. cies of the Oenochrominae s. l., Taxeotis lechrioschema ala.org.au/). Systematics on the Geometridae has Turner, 1939 was collected. This species has not been benefited from this project from financial support collected since F. Walker took the first specimens given to research describing new species collected in Merredin, WA, in September and October 1938, on Bush Blitz Surveys. and, to date, the species has only been known from Selected major findings for the Geometridae from these five specimens all designated as types by A. seven Bush Blitz surveys, three in Western Australia J. Turner in the same year. (WA) and four in Tasmania, in which Geometridae were a target group are as follows: 3) Tasmania 2014 – Flinders Island 35 species of Geometridae in 41 genera with five 1) WA 2009 – semi-arid wheatbelt area in southwest new species. WA The results from this survey have not been fully 56 species (25 genera). documented but this remote area of Tasmania was The percentage of undescribed species collected was notable for the number of new records for the state. very high at 70 % and consisted of 39 unidentified Rare species collected were Casbia oenias (Meyrick, Geometridae with eight new to science. The genus 1892), Chrysolarentia ptochopis (Turner, 1907) and Dichromodes Guenée, 1858 was particularly diverse Epyaxa agelasta (Turner, 1904). In addition a rare with 15 new species and 4 new to science. Dichro- known undescribed species of the Hepialidae from modes is the largest Australian genus of Geometridae the genus Fraus Walker, 1856 was collected. This with 70 described species and around 100 new or species is known from only five specimens collected undescribed species. It is arguably one of the most on the mainland of Tasmania from one collection unresolved genera taxonomically because of the event in 1986. large number of undescribed species in the genus and the likelihood of many synonyms due to the Four generic revisions of Geometridae including cryptic colour and wing patterns of specimens. They descriptions of new species collected in Bush Blitz are particularly diverse in the semi-arid interior of surveys, funded through the Bush Blitz Project, Australia. conducted by the primary author have been: – Redescription of Omoplatica Turner, 1926 (Geo- metridae: Oenochrominae s. str.) from the semi- arid interior of Western Australia, with descrip-

253 ©Zoologische Staatssammlung München/Verlag Friedrich Pfeil; download www.pfeil-verlag.de

tion of three new species and re-description of Mutanen, M., Wahlberg, N. & Kaila, L. 2010. Compre- the type species, all endemic to WA. All species hensive gene and taxon coverage elucidates radia- in this genus are rare apart from one species tion patterns in moths and butterflies. Proceedings which is commonly collected in the semi-arid of the Royal Society B 277: 2839-2848. doi:10.1098/ interior of WA. The type species is only known rspb.2010.0392 Regier, J. C., Zwick, A., Cummings, M. P., Kawahara, A. from eight specimens from two collecting trips Y., Cho, S., Weller, S., Roe, A., Baixeras, J., Brown, in the wheat-belt of WA. One undescribed spe- J. W., Parr, C., Davis, D. R., Epstein, M., Hallwachs, cies is only known from one location and another W., Hausmann, A., Janzen, D. H., Kitching, I. J., from three specimens from two locations again Solis, A. M., Yen, S., Bazinet, A. L. & Mitter, C. 2009. from the wheatbelt in WA. The remaining new Toward reconstructing the evolution of advanced species a large showy moth was collected in moths and butterflies (Lepidoptera: Ditrysia): an spring on a Bush Blitz expedition and is reaso- initial molecular study. BMC Evolutionary Biology nably well-represented in collections. 9: 280. doi:10.1186/1471-2148-9-280 – Redescription of Lipogya Warren, 1898 (Geome- Sihvonen, P., Mutanen, M., Kaila, L., Brehm, G., Haus- tridae: Boarmiini) with the description of two mann, A. & Staude, H. S. 2011. Comprehensive new species, and redescription of three species. molecular sampling yields a robust phylogeny for geometrid moths (Lepidoptera: Geometridae). PLoS – Redescription of Nisista Walker, 1860 (Geome- ONE 6(6): e20356. doi:10.1371/journal.pone.0020356 tridae: Nacophorini) with the description of five Yamamoto, S. & Sota, T. 2007. Phylogeny of the Geo new species and the redescription of three spe- metridae and the evolution of winter moths inferred cies. from a simultaneous analysis of mitochondrial and – Redescription of Scioglyptis Guest, 1887 (Geome- nuclear genes. Molecular Phylogenetics and Evolu- tridae: Boarmiini) with the description of four tion 44: 711-723. new species and the redescription of six species. Young, C. J. 2006. Molecular relationships of the Aus- tralian Ennominae (Lepidoptera: Geometridae) and Atlas of Living Australia 2014. Sharing biodiversity implications for the phylogeny of the Geometridae knowledge. http://www.ala.org.au/ [accessed 06- from molecular and morphological data. Zootaxa Oct-2014]. 1264: 1-147. Minet, J. 1983. Étude morphologique et phylogenetique – – 2008. Characterisation of the Australian Nacopho des organes tympaniques des Pyraloidea. 1. Gen- rini using adult morphology and phylogeny of the eralites et homologies. (Lep. Glossata). Annales Geometridae based on morphological characters. Societe Entomologique de France 19: 175-207. Zootaxa 1736: 1-141.

On the Phylogeny and Systematics of the tribe Larentiini (Lepidoptera: Geometridae)

Andro Truuverk & Erki Õunap

Truuverk, A. & Õunap, E. 2014. On the phylogeny and systematics of the tribe Larentiini (Lepidoptera: Geometridae). P. 254 in: Hausmann, A. (ed.). Proceedings of the eighth Forum Herbulot 2014. How to accelerate the inventory of biodiversity (Schlet- tau, 30 June – 4 July 2014). Spixiana 37 (2). Andro Truuverk (corresponding author), Institute of Ecology and Earth Sciences, University of Tartu, Vanemuise 46, Estonia; e-mail: [email protected]

Hereby we concentrated on resolving the phylog- dehydrogenase (MDH), glyceraldehyde-3-phosphate eny of tribe Larentiini and its relationships with dehydrogenase (GAPDH), isocitrate dehydrogenase other tribes from the subfamily Larentiinae. In (IDH) and wingless (WGL). The total length of the total, 63 species from 22 tribes were included into data matrix was 7264 bp. Our results demonstrate the analysis. 12 species from 10 genera belonged that the tribe Larentiini within its current limits is to the tribe Larentiini according to the recent clas- not monophyletic. Indeed, majority of the studied sification. Sequence data from one mitochondrial larentiine genera formed a well-supported mono- and eight nuclear genes were used: cytochrome phyletic lineage together with Larentia Treitschke, oxidase subunit 1 (COI), 28S rRNA (expansion seg- 1825, the type genus of the tribe. However, three ments D1 & D2), elongation factor 1 alpha (EF-1α), genera were placed into different sub-lineages of ribosomal protein S5 (RpS5), carbamoylphosphate the subfamily Larentiinae. synthase domain protein (CAD), cytosolic malate

254 ©Zoologische Staatssammlung München/Verlag Friedrich Pfeil; download www.pfeil-verlag.de

Molecular and morphological phylogenies in geometroid lepidopterans (Lepidoptera, Geometriformes) – discordant or concordant

Evgeny A. Beljaev

Beljaev, E. A. 2014. Molecular and morphological phylogenies in geometroid lepidopterans (Lepidoptera, Geometriformes) – discordant or concordant. Pp. 255-258 in: Hausmann, A. (ed.). Proceedings of the eighth Forum Herbulot 2014. How to accelerate the inventory of biodiversity (Schlettau, 30 June – 4 July 2014). Spixiana 37 (2). Evgeny A. Beljaev, Institute of Biology and Soil Science, Far Eastern Branch of Russian Academy of Sciences, Sto Let Vladi vostoku str. 159, Vladivostok, 690022, Russia; e-mail: [email protected]

Comparative analysis of modern morphological and Four recent molecular-phylogenetic studies were molecular phylogenies in geometroid lepidopterans included in the analysis. The first two were focused is made. This group includes a number of mainly on Geometridae (Yamamoto & Sota 2007, Sihvonen et nocturnal macrolepidopteran families – Cimeliidae, al. 2011). The other two covered all Lepidoptera (Re- Sematuridae, Epicopeiidae, Drepanidae, Uraniidae gier et al. 2009, Mutanen et al. 2010), and I took from and Geometridae, which were united in series Geo them only the portions with geometroid families. metriformes by Kuznetzov & Stekolnikov (2001). This The resulting phylogenetic trees in both publication series corresponds to the drepanoid/geometroid sets are generally similar in branching pattern. In assemblage plus superfamily Cimelioidea following the each molecular phylogeny all basal nodes (ap- Minet & Scoble (1998). Geometriformes are one of the proximately up to tribal level) were separated into largest taxonomic groups in Lepidoptera, numbering 3 groups. First – nodes that are congruent with my nearly 25 thousand described species. Numerous morphological notions on cladistic relationships of questions about relationships of geometroid lepido relevant taxa (called here for clarity as ‘green’ nodes; pterans at all taxonomic levels are still far from solved. in Fig. 1 reproduced in grey); second – nodes that Morphological data for this analysis was taken differ from my morphological notions (‘red’ nodes; from my morphological and phylogenetic research in Fig. 1 in dark grey); and third – nodes that are of the geometrid moths and related families that omitted from the analysis either due to me lacking had been partially published in a series of papers an opportunity to examine relevant taxa or because (Beljaev 1992, 1997, 1998a, 1998b, 2000, 2003a, 2003b, morphological data were insufficient for clarifying 2006a, 2006b, 2007, 2008b, 2009a, 2009b) and in a book their phylogenetic position (‘white’ nodes). (Beljaev 2008a). Most of these works are based on the Also, all selected ‘colour’ nodes were divided combination of functional-morphological analysis into 2 groups: with bootstrap support values 50 (mainly following Kuznetzov & Stekolnikov 2001) and more, and less than 50 (Table 1, Fig. 1.). Nodes and manual cladistics. The principal theoretical point with low bootstrap support values (usually less than of my reconstruction of the phylogeny in Geometri- 50) are ambiguous for indication of phylogenetic formes is the statement, that “apomorphy – is not a relationship, and they commonly referred to as area character state but a fact that this state was acquired of low resolution or unresolved nodes. For short, once” (formulated in Russian by Rasnitsyn 2002: 74). below I shall name nodes from the first group as This understanding of apomorphy does not permit resolved nodes, and nodes from the second group us to take a morphological character as is, without as unresolved nodes. prior analysis of possible origins and transforma- As can be seen from Table 1 (columns 3, 4), tion; it implies deep comparative-morphological ‘red’ nodes account for 30-40 % of the phylogenies analysis focused on identification of morphological and their percentage is comparable with the share homologies and on construction of polarized rows of ‘green’ nodes, which account for 48-52 % of all of morphological transformations (morphoclines); it tested nodes. The only exception is the phylogeny by requires stringent selection of characters that carry Yamamoto & Sota (2007) with 10 % of the nodes being ‘phylogenic signal’ at the targeted taxonomic level ‘red’ and 79 % being ‘green’). This ratio indicates prior to the formulation of hypotheses about prob- low concordance between the morphological and able synapomorphies; it entails manual reconstruc- molecular phylogenetic data and calls into question tion of a phylogenic tree that is consistent with a the results of one or both studies. priori selected characters. That is, this understanding However, if we exclude the nodes with bootstrap of an apomorphy requires it to be considered not support values less than 50 from our calculations, as a logical construction, but as a morphological the results will look quite differently. The rate of innovation with its own history. ‘red’ nodes drops to 7-19 % and becomes much less

255 ©Zoologische Staatssammlung München/Verlag Friedrich Pfeil; download www.pfeil-verlag.de

Fig. 1. Percentage of ‘white’, ‘green’ and ‘red’ resolved nodes (A) and unresolved nodes (B) in phylogenies by Yamamoto & Sota (2007), Sihvonen et al. (2011), Regier et al. (2009) and Mutanen et al. (2010). than the ratio of ‘green’ nodes, which account for phylogenies of the geometroid lepidopterans demon- 60-86 % of all tested nodes excluding the nodes in strate rather good concordance when tree nodes have the ‘grey’ area (Table 1, columns 8 and 9; Fig. 1A). high bootstrap support values (at least when more Percentage of ‘white’, ‘green’ and ‘red’ nodes with than 50). The exceptions are rare and require targeted bootstrap support values less than 50 is illustrated on research using both – molecular and morphological Figure 1B. It is clear that ‘red’ nodes are absolutely approaches. Discrepancies between molecular and predominant in this area. morphological phylogenies within the area of nodes In the phylogeny by Sihvonen et al. (2011), the with low bootstrap support values cannot be used rate of ‘green’ nodes is comparatively low – only 60 % as the argument for rejection of relationships estab- of all tested nodes with bootstrap support values lished on the basis of morphological criteria and for 50 and more, and the share of ‘red’ nodes reaches revision of taxonomic systems. almost one-fourth of ‘green’ nodes (24 %). This is Noteworthily, this concordance was attained for a result of a large percentage of morphologically phylogenies reconstructed by entirely different ways: unresolved ‘white’ nodes, which account for 26 % by formal quantitative methods for molecular data of all nodes outside of the ‘grey’ area. However, I and by logic analysis for morphological data. This expect that most of them could reflect true phyloge- indicates that morphological data are consistent with netic relationships, taking into account appearance logic construction of phylogenetic trees, which re- of moths and their superficial morphology. quires the preliminary selection (a priori weighting) Thus, modern morphological and molecular of characters based on the previous knowledge about

Table 1. Congruence of nodes in the molecular phylogenies with morphological phylogenetic hypothesis. Percentages are rounded to whole numbers.

All tested nodes: Resolved nodes: number, ‘colour’ type and percentage number, ‘colour’ type and percentage N Author of Number of Number Number Number Number Number Number Number molecular all tested of ‘white’ of ‘green’ of ‘red’ of tested of ‘white’ of ‘green’ of ‘red’ phylogeny nodes nodes / % nodes / % nodes / % nodes nodes / % nodes / % nodes / % 1 2 3 4 5 6 7 8 9 1. Yamamoto 29 3 / 10 % 23 / 79 % 3 / 10 % 27 2 / 7 % 23 / 86 % 2 / 7 % & Sota 2007 2. Sihvonen 67 14 / 21 % 33 / 49 % 20 / 30 % 42 11 / 26 % 25 / 60 % 6 / 14 % et al. 2011 3. Regier 23 2 / 9 % 12 / 52 % 9 / 39 % 14 2 / 14 % 11 / 79 % 1 / 7 % et al. 2009 4. Mutanen 25 3 / 12 % 12 / 48 % 10 / 40 % 16 2 / 12 % 11 / 69 % 3 / 19 % et al. 2010

256 ©Zoologische Staatssammlung München/Verlag Friedrich Pfeil; download www.pfeil-verlag.de the probability and probable directions of certain – – 2006a. A morphological approach to the Ennominae morphological transformations. This corresponds phylogeny (Lepidoptera, Geometridae). Spixiana to the informal subjective nature of morphological 29: 215-216. character as hypotheses about similarity or differ- – – 2006b. Tentative tribal system of Ennominae based on ence between the homologous morphostructures of current family-group names. http://www.herbulot. de/pdf/Family_group_names_in_Geometridae_al- different organisms. Also, only the combination of ternative_12_06_2007.pdf/ [accessed 03-Apr-2013] functional-morphological method, manual cladistic – – 2007. Taxonomic changes in the emerald moths technology and historical understanding of apomor- (Lepidoptera: Geometridae, Geometrinae) of East phy, provides maximal concordance between the Asia, with notes on the systematics and phylogeny morphological and molecular phylogenies. of Hemitheini. Zootaxa 1584: 55-68. The area of nodes with low bootstrap support – – 2008a. Phylogenetic relationships of the family Geo values in molecular phylogenies generally more or metridae and its subfamilies. Meetings in memory less coincides with taxonomic groups which are also of N. A. Cholodkovsky 60, 238 pp., St.-Petersburg difficult for morphological phylogenetic analysis. (Zoological Institute RASS) [in Russian with English Obviously, this coincidence is not accidental and Summary]. results from the loss of clearness of the ‘phylogenetic – – 2008b. A new concept of the generic composition of the geometrid moths tribe Ennomini (Lepidoptera: signal’ at both levels of the organization of organisms Geometridae) based on functional morphology of or from the peculiarities of divergence on the early the male genitalia. Entomologicheskoe Obothrenie stages of the ‘maturing’ of taxa. However, within 87: 152-165 [in Russian; translation in English: En- this area of molecular phylogenies, nodes established tomological Review 88: 50-60, 2008]. morphologically appear to be more reliable than – – 2009a. Phylogenetic relationships of the geometroid branching pattern in the molecular trees. lepidopterans (Lepidoptera: Cimeliidae, Epicopei idae, Sematuridae, Drepanidae, Uraniidae, Geo I express my gratitude to Evgeny Zakharov (University metridae). Spixiana 32: 23-24. of Guelph, Ontario) for the discussion of this work. This – – 2009b. Phylogenetic position of the tribe Azelinini work was sponsored partially by grants from the Far- (Lepidoptera: Geometridae, Ennominae) based on Eastern Branch of Russian Academy of Sciences No. functional morphology of the male genitalia. Euro 12-II-0-06-019 and No. 12-III-A-06-078. asian Entomological Journal 8: 82-84. Kuznetzov, V. I. & Stekolnikov, A. A. 2001. New ap- Beljav, E. A. 1992. Comparative analysis of phylogenetic proaches to the system of Lepidoptera of world and statistic methods on the sample of geometrids fauna (on the basis of the functional morphology of the genera Euchristophia Fletch. and Cabera Tr. of the abdomen). Trudy Zoologicheskogo Instituta (Lepidoptera, Geometridae). A. I. Kurentzov’s An- 282, 462 pp., St. Petersburg (Nauka) [in Russian nual Memorial Meetings 3: 52-63 [in Russian]. with English Summary]. – – 1997. A new genus and new species of the Ennomi- Mutanen, M., Wahlberg, N. & Kaila, L. 2010. Compre- nae (Lepidoptera, Geometridae) from Russian Far hensive gene and taxon coverage elucidates radia- East, with remarks on the phylogeny of the related tion patterns in moths and butterflies. Proceedings genera. Tinea 15: 125-130. of the Royal Society B (Biological Sciences): 1-10. – – 1998a. Morphology of copulatory apparatus in doi:10.1098/rspb.0392 Devenilia corearia and description of a new tribe De- Minet, J. & Scoble, M. J. 1998. The geometroid/drepa- veniliini (Lepidoptera, Geometridae, Ennominae). noid assemblage. Pp. 301-320 in: Kristensen, N. P. Zoologicheskij Zhurnal 77 (4): 438-443 [in Russian; (ed.). Lepidoptera, moths & butterflies, 1. Hand- translation in English: Entomological Review 78: book of Zoology 4 (35), “1999”, Berlin (Walter de 517-521, 1998]. Gruyter). – – 1998b. A new genus of the Ennominae from East Sihvonen, P., Mutanen, M., Kaila, L., Brehm, G., Haus- Asia, with notes on the phylogeny of some Holarctic mann, A. & Staude, H. S. 2011. Comprehensive Anagogoni (Lepidoptera, Geometridae). Tinea 15: molecular sampling yields a robust phylogeny for 266-270. geometrid moths (Lepidoptera: Geometridae). PLoS – – 2000. Remarkable new genus and new species of ONE 6(6): e20356. doi:10.1371/journal.pone.0020356 the geometrid moths from Central Asia, related to Rasnitsyn, A. P. 2002. The process of evolution and the genus Desertobia Viidallepp, 1989 (Lepidoptera, methodology of taxonomy. Trudy Russkogo Ento Geometridae, Ennominae) with notes on the tax- mologicheskogo Obshchestva 73: 1-108 [In Rus- onomy of the Desertobiini. Tinea 16: 240-245. sian]. – – 2003a. Phylogenetic significance of skeleton-mus- Regier, J. C., Zwick, A., Cummings, M. P., Kawahara, A. cular anatomy of the genitalia in Geometridae. Y., Cho, S., Weller, S., Roe, A., Baixeras, J., Brown, Spixiana 26: 206-207. J. W., Parr, C., Davis, D. R., Epstein, M., Hallwachs, – – 2003b. Notes to the molecular phylogeny of the W., Hausmann, A., Janzen, D. H., Kitching, I. J., So- Geometridae. Spixiana 26: 208. lis, M. A., Yen, S.-H., Bazinet, A. L. & Mitter, C. 2009. Toward reconstructing the evolution of advanced

257 ©Zoologische Staatssammlung München/Verlag Friedrich Pfeil; download www.pfeil-verlag.de

moths and butterflies (Lepidoptera: Ditrysia): an tridae and the evolution of winter moths inferred initial molecular study. BMC Evolutionary Biology from a simultaneous analysis of mitochondrial and 9: 280, 21 pp. doi:10.1186/1471-2148-9-280 nuclear genes. Molecular Phylogenetics and Evolu- Yamamoto, S. & Sota, T. 2007. Phylogeny of the Geome tion 44: 711-723.

Molecular and morphological investigations suggest family level for the little known Pseudobiston pinratanai Inoue, 1994

Hossein Rajaei, Carola Greve, Harald Letsch, Dieter Stüning, Niklas Wahlberg, Joël Minet & Bernhard Misof

Rajaei, H., Greve, C., Letsch, H., Stüning, D., Wahlberg, N., Minet, J. & Misof, B. 2014. Molecular and morphological investigations suggest family level for the little known Pseudobiston pinratanai Inoue, 1994. P. 258 in: Hausmann, A. (ed.). Proceedings of the eighth Forum Herbulot 2014. How to accelerate the inventory of biodiversity (Schlettau, 30 June – 4 July 2014). Spixiana 37 (2). Hossein Rajaei (corresponding author), Biocentre Grindel and Zoological Museum, University of Hamburg, Martin-Luther- King-Platz 3, 20146 Hamburg, Germany; e-mail: [email protected]

After the description of Pseudobiston pinratanai Inoue, families. All phylogenetic analyses (Maximum likeli- 1994 within the Geometridae, the family placement of hood, Parsimony and Bayesian inference) revealed this enigmatic, oriental species has been questioned a strongly supported sister-group relationship be- by different authors. Although a complete lack of tween Pseudobiston and the Epicopeiidae, suggesting abdominal tympanal organs strongly suggested that the former would deserve its own family (new a non-geometrid taxon, the other morphological taxon in prep.). This hypothesis could be supported characters of P. pinratanai were initially considered by following synapomorphies of Pseudobistonidae poorly informative with regard to any tentative + Epicopeiidae: I) strong reduction or absence of family assignment. Then, in order to elucidate this ocelli; II) relatively short tibia of hindleg; III) vertical systematic position, we used a large molecular flexion zone across the metepimeron; IV) a broad dataset (sequences of eight genes including one mi- furco-epimeral bands on metathorax; V) posterior tochondrial gene (COI) and seven nuclear genes: EF- foramen in dorsal position of euphragma; VI) ante- 1α, Wingless, RpS5, MDH, GAPDH, CAD and IDH) rolateral processes of the second sternum arched in taking into account P. pinratanai and 111 other spe- lateral view; VII) juxta of male genitalia, possess a cies, mostly members of various macroheteroceran pair of long, sclerotized excrescences.

Enigmatic cycad moths of Africa: a holistic approach to examine their systematic position (Lepidoptera, Geometridae)

Pasi Sihvonen, Hermann S. Staude & M. Mutanen

Sihvonen, P., Staude, H. S. & Mutanen, M. 2014. Enigmatic cycad moths of Africa: a holistic approach to examine their systematic position (Lepidoptera, Geometridae). P. 258 in: Hausmann, A. (ed.). Proceedings of the eighth Forum Herbulot 2014. How to accelerate the inventory of biodiversity (Schlettau, 30 June – 4 July 2014). Spixiana 37 (2). Pasi Sihvonen (corresponding author), Käärmekuusenpolku 4 C 11, 02880 Veikkola, Finland; Research Affairs, P.O. Box 33, 00014, University of Helsinki, Finland; e-mail: [email protected]

The systematic position and hierarchical level of the trices were analysed and phylogenetic trees were moth taxon Diptychini Janse, 1933 (the cycad moths) constructed using model-based methods (Bayesian have remained controversial and largely uninvesti- inference). The molecular results were placed in a gated (Lepidoptera: Geometridae). The uncertainty larger framework through extensive morphological is partially due to their unique morphological, bio- examinations. We demonstrate that the Diptychini logical and behavioural characteristics. To examine belong to the Geometridae subfamily Ennominae, these questions, comprehensive molecular analyses pinpoint its more exact position within the subfamily, of eight genes, representing over 100 Geometroidea and identify its potential relative taxa. The results and taxa, were carried out in a global context. Data ma- their significance are discussed in the global context.

258 ©Zoologische Staatssammlung München/Verlag Friedrich Pfeil; download www.pfeil-verlag.de

Recent advances in the knowledge of Geometrid moths of Ethiopia

Andrea Sciarretta, Axel Hausmann & Francesco Parisi

Sciarretta, A., Hausmann, A. & Parisi, F. 2014. Recent advances in the knowledge of Geometrid moths of Ethiopia. P. 259 in: Hausmann, A. (ed.). Proceedings of the eighth Forum Herbulot 2014. How to accelerate the inventory of biodiversity (Schlettau, 30 June – 4 July 2014). Spixiana 37 (2). Andrea Sciarretta (corresponding author), Department of Agricultural, Environmental and Food Sciences, University of Molise, Via De Sanctis, 86100 Campobasso, Italy; e-mail: [email protected]

Due to the geographical position and orogenic his- DNA barcoding suggests the number of Ethiopian tory of Eastern Africa, Ethiopia constitutes a unique geometrid species to exceed 600 species. So far, no arrange of natural habitats characterized by extreme- comprehensive study on the fauna of this country ly different climatic and environmental conditions. has been published. The Ethiopian highlands contribute to more than The studies of the authors are based on thousands 50 % of the land area with Afromontane vegetation of Ethiopian geometrid moths in their collections, and, due to its isolation from other mountain systems offering a good starting point for reviewing the of Africa, it has been acting over millions of years historical descriptions and for providing additional as a real “laboratory of evolution”, thus leading to data. The first focus was laid on the subfamily Ge- a high percentage of endemic plants and animals. ometrinae, so far revealing more than 95 species Despite this, the knowledge of Lepidopteran which were assessed in an integrative taxonomic biodiversity in the country is very scarce and this approach combining classical morphological and is particularly true for the family Geometridae. So molecular (DNA Barcoding) methods. Particularly far, 90 taxa have been described from Ethiopia of significant is the case of the genus Prasinocyma War- which 79 are currently accepted as valid at species ren, 1897, with 44 species currently identified for the rank. A rough estimate based on the study of col- fauna of Ethiopia, of which at least 22 are new for lection material involving both morphology and science.

A complex diversity of taxa behind one species: Lophophelma luteipes Felder, 1875

Claude Tautel

Tautel, C. 2014. A complex diversity of taxa behind one species: Lophophelma luteipes Felder, 1875. P. 259 in: Hausmann, A. (ed.). Proceedings of the eighth Forum Herbulot 2014. How to accelerate the inventory of biodiversity (Schlettau, 30 June – 4 July 2014). Spixiana 37 (2). Claude Tautel, 272 rue du Faubourg-Saint-Antoine, 75012 Paris, France; e-mail: [email protected]

The Asian geometrid moth Lophophelma luteipes correlated to differences in the coloration of the wing Felder, 1875 (Geometrinae) has been considered (e. g. undersides. Morphological and genetic differences by Holloway, 1996) a rather homogeneous species in both groups point to a wide diversity of taxa (on with the similar but different species L. ruficosta species or subspecies level) behind L. luteipes as cur- (Hampson, 1891) (S. India) and another not yet rently understood. The fact that both groups occur named one in Sulawesi. Barcoding results (in BOLD) sympatricly in Vietnam, Malaysia (Borneo), Sumatra, of a number of specimens yielded, however, at least and Java is an interesting biogeographical feature. four different BINs. As many specimens as possible Since the unique holotype of L. luteipes is a female, it were examined and genitalia slides were made of seems important to study also the morphology of the specimens from N.W. and N.E. India, Sri Lanka, female genitalia of representative specimens from all N. and S. Thailand, Cambodia, N. and S. Vietnam, involved regions, what was not yet completely pos- Hong Kong, Mainland Malaysia and Sabah, N. and sible. Pictures of specimens (habitus and underside) W. Sumatra, Palawan, Jawa, and Sulawesi. The from all regions involved, of genitalia slides, and morphological structures in the genitalia turn out maps of distribution were presented. Publication is to be surprisingly diverse and group, grosso modo, planned for early 2015. in two very distinct pattern groups which are also

Advances in the knowledge of the larentiine fauna of southern Italy by DNA barcoding (Lepidoptera, Geometridae)

Stefano Scalercio, Marco Infusino & Axel Hausmann

Scalercio, S., Infusino, M. & Hausmann, A. 2014. Advances in the knowledge of the larentiine fauna of southern Italy by DNA barcoding (Lepidoptera, Geometridae). P. 260 in: Hausmann, A. (ed.). Proceedings of the eighth Forum Herbulot 2014. How to accelerate the inventory of biodiversity (Schlettau, 30 June – 4 July 2014). Spixiana 37 (2). Stefano Scalercio (corresponding author), Consiglio per la Ricerca e la sperimentazione in Agricoltura, Unità di Ricerca per la Selvicoltura in Ambiente Mediterraneo, contrada Li Rocchi, 87036 Rende (Cosenza), Italy; e-mail: [email protected]

The lepidopteran fauna of southern Italy receives distance. Similarly, Coenotephria antonii Hausmann, growing interest due to its peculiar biogeography 2011 was recently separated from Coenotephria and its ecological vulnerability. In this area sev- tophaceata (Denis & Schiffermüller, 1775) and sup- eral species have their southernmost distributional posed to be its central and southern Italian vicariant. boundary and are prone to climate changes. Many However, both species were recently found to occur populations will be submitted to an immediate sympatrically (though appearing rather asynchro- threat due to climate warming expected for the next nously) in central and southern Italy, genetically decades. Other species have their northernmost diverging by 6.6 %. distributional boundary here and may colonize For the fauna of Sicily and southern Calabria, Europe northwards as a consequence of increas- barcoding analysis allowed a correct identification ing mean temperatures during the next decades. of Eupithecia cocciferata Millière, 1864, previously Along the Italian peninsula the populations of identified as E. lentiscata Mabille, 1869, and they al- several species were reproductively isolated from lowed to certainly attribute some Sicilian specimens the other European populations and sometimes to Triphosa dubitata (Linnaeus, 1758) which had been diverge consistently from a genetic point of view. attributed to Triphosa tauteli Leraut, 2008, previously. Recent studies on DNA barcoding in southern Italy DNA barcoding allows us also to carry out correct resolved various taxonomic questions on Larentiinae specific attributions of specimens belonging to taxo- (Lepidoptera Geometridae), and strongly improved nomically ‘complicated’ species such as Xanthorhoe the knowledge of its fauna. disjunctaria (la Harpe, 1860), Coenotephria ablutaria Hydriomena sanfilensis (Stauder, 1915) was raised (Boisduval, 1840), Epirrita christyi (Allen, 1906), to species rank from synonymy (Hausmann & Eupithecia linariata (Denis & Schiffermüller, 1775). Viidalepp 2012). The nearest species is Hydriomena Furthermore, new questions arose from DNA impluviata (Denis & Schiffermüller, 1775) at a genetic barcoding analyses. Further studies are required to distance (COI, barcode region) of 4.0 %. This species examine the taxonomic status of Italian populations of is endemic to southern Italy. Through DNA barcod- Colostygia sericeata (Schwingenschuss, 1926), currently ing we have been able to identify a larva, found in a validated as C. sericeata subsp. holli (Prout, 1938), and spun leave of Rosa canina, as H. sanfilensis, which is to investigate the genetic difference (2.5 %) between the first record of a host-plant for this species. Nebula European and southern Italian populations of Lam- carlae Hausmann, 2011 from central and southern propteryx suffumata (Denis & Schiffermüller, 1775), Italy was described as an allopatric sister species of a genetically very homogeneous species all over the Nebula achromaria (la Harpe, 1853) at 3.2 % genetic rest of Europe, Altai mountains and North America.

Palyadini systematics, state of the art

Glaucia Marconato

Marconato, G. 2014. Palyadini systematics, state of the art. Pp. 260-261 in: Hausmann, A. (ed.). Proceedings of the eighth Forum Herbulot 2014. How to accelerate the inventory of biodiversity (Schlettau, 30 June – 4 July 2014). Spixiana 37 (2). Glaucia Marconato, Estância Vale Verde, CEP 13690-000, Descalvado, São Paulo, Brazil; e-mail: [email protected]

Palyadini, a tribe of Ennominae, are characterized are distributed in the Neotropics from Argentina to by the absence of frenulum and retinaculum and the the southern United States. In the current concept, presence of golden scales composing metallic points six genera are included in Palyadini: Palyas Guenée, and lines on the upper side of wings. 115 valid species 1858, Phrygionis Hübner, 1825, Pityeja Walker, 1861,

Argyrotome Warren, 1894, Opisthoxia Hübner, 1825 The alpha-taxonomy and phylogeny of the larg- and Ophthalmoblysis Scoble, 1995. This group was est genus Opisthoxia with almost 90 species largely proposed by Guenée (1858) (as “Palyade”), includ- remained untreated. Currently, the phylogeny of the ing Eumelea Duncan, 1841, Palyas, Ophthalmophora tribe is analysed in an integrated approach combin- Guenée, 1858 and Byssodes Guenée, 1858. Hulst ing morphological and molecular characters. The (1896), has noticed that all the species of Palyas and challenge was to find sufficient (fresh) material, and Phrygionis, which occur in the USA, did not have some taxa are very rare in museums (some of them frenulum and retinaculum. Later, Warren included being potential synonyms). In the genus Opisthoxia, it in the tribe Baptini. which is supposed to harbour many cryptic species, Warren described four species in Argyrotome, species delimitation is particularly difficult because seven species in Ophthalmophora and seven in Opisth- of great similarity and insufficient number of valu- oxia. Oberthür (1916) reviewed the genera Palyas, able differential features in morphology. Therefore Ophthalmophora and Byssodes. He followed Guenée DNA barcodes were chosen as an additional charac- and cited Eumelea as a part of the group “Palyade”. ter set for supporting species delineation (identifying Dognin described one Argyrotome and five Ophthal- synonyms and cryptic species) and, consequently, mophora species. Schaus described two more new warranting a robust phylogenetic analysis. species of Argyrotome. Prout (1933) revised the genus Phrygionis and Debauche (1937) splitted Argyrotome Debauche, H. 1937. Geometridae nouveaux ou peu con- into two subgenera: Argyrotome and Parargyrotome. nus d’Amerique du Sud. Bulletin du Musee Royal Holloway (1993, 1996) recognized Palyadini as a d’Histoire Naturelle de Belgique 13 (14): 1-28. separate tribe from Baptini and definitively excluded Guenée, A. 1857-1858. Uranides et Phalénites I.-II. In: the south-east Asian Eumeleini from Ennominae Boisduval, M. M. & Guenée, M. A. Histoire naturelle des insectes, species général des Lépidoptères. Tome (with genus Eumelea which earlier had been regarded IX-X. Paris (Librarie Encyclopédique de Roret). to be related to Palyadini). Holloway, J. D. 1993 [1994]. The moths of Borneo: fam- In 1994, Scoble reviewed two genera Phrygionis ily Geometridae, subfamily Ennominae. 309 pp., and Pityeja; one year later, the same author revised London. the tribe, without, however, performing a phyloge- – – 1996. The moths of Borneo: family Geometridae, netic analysis. He synonymized Ratiaria Walker, 1861 subfamilies Oenochrominae, Desmobathrinae and with Phrygionis, and the two genera Aplorama War- Geometrinae. Malayan Nature Journal 49: 147-326. ren, 1904 and Callurapteryx Warren, 1894 with Pityeja, Hulst, G. D. 1896. A classification of the Geometrina of describing several new species e transferring many North América, with descriptions of new genera others to these two genera. A new genus was pro- and species. Transactions of the American Entomo- posed, Ophthalmoblysis. Moreover, Ophthalmophora logical Society 23: 245-386, pls 10-11. Oberthür, C. 1916. Famille Palyadae. Études Lépidopté- and Argyroplutodes Warren, 1894 were synonymized rologie Comparée 12: 125-149. with Opisthoxia and Parargyrotome with Argyrotome. Prout, L. B. 1933. On the geometrid genus Phrygionis Hb. Scoble (1994) discusses also the wing patterns of Novitates Zoologicae 39: 1-9. Opisthoxia species and suggests species groups based on these patterns.

Family ranking in Lepidoptera communities in southwestern Africa: are Geometridae statistically important?

Wolfram Mey

Mey, W. 2014. Family ranking in Lepidoptera communities in southwestern Africa: are Geometridae statistically important? Pp. 261-263 in: Hausmann, A. (ed.). Proceedings of the eighth Forum Herbulot 2014. How to accelerate the inventory of biodiversity (Schlettau, 30 June – 4 July 2014). Spixiana 37 (2). Wolfram Mey, Museum für Naturkunde, Leibniz Institut für Evolutions- und Biodiversitätsforschung, Invalidenstr. 43, 10115 Berlin, Germany; e-mail: [email protected]

Lepidoptera are one of the mega-diverse orders of who are specialists of a superfamily, a single family insects. There are no Lepidoptera taxonomists who or even a single genus. Fieldwork being performed are able to work on all or most groups. The huge by these specialists follows the same pattern: they number of existing species needs specialisation. usually collect specimens from their groups and Today, taxonomic work is done by entomologists, disregard the rest. This kind of specialisation, un-

0 1 2 3 4 5 6 7 10 rank Geometridae within total sample (n = 43) Geometridae within Macros Fig. 1. Rank-abundance plot of Geometridae in light trap samples.

Fig. 2. Map of southwestern Africa (BIOTA project area) fortunately, has the disadvantage of preventing a depicting the proportion (%) of Geometridae species in general view on local Lepidoptera communities and light trap samples taken in five different biomes. of ignoring ecological contexts. Right from the beginning of the faunistic explo- The Geometridae is one of the most dominant ration of southwestern Africa (Namibia, western families in southwestern Africa concerning species RSA) a holistic approach was applied towards the and specimens numbers. The family belongs to collecting and processing methodology. By using the Macrolepidoptera, and in this group it takes automatic light traps the entire spectrum of Lepi- the second rank in species numbers. At the time of doptera was sampled and subsequently studied. All analyzing the light trap catches, the Noctuidae was individuals of a sample were counted and sorted recognised as the largest family and consequently to species, which were identified at first to family took the first rank. Today, the Noctuidae are split level, later to morphospecies and species levels. In into several families, and future analyses will prob- this way frequency and abundance distribution of ably demonstrate, that all families in the Noctuoidea species were preserved, which is an intrinsic source superfamily fall behind Geometridae taking rank of data included in each sample. two or less. Most of the results were published in Mey (2011). When considering the whole Lepidoptera spec- These data are used here to analyse and demonstrate trum Gelechiidae and Pyralidae: Phycititinae of the the statistical rank of the Geometridae as one family Microlepidoptera are similarly speciose and even among many others in Lepidoptera communities of occupy the first rank sometimes. about 40 localities distributed in the major biomes In Savanna and Nama-Karoo localities in Na- of southwestern Africa. mibia and RSA Geometridae species make up about

Table 1. Portions of Geometridae in light trap samples taken in five biomes in southwestern Africa.

total species number Geometridae species number Biome localities min. max. mean min. max. mean Savanna 14 93 382 219 7 42 20 Nama-Karoo 13 63 158 108 2 19 9 Desert 8 13 95 39 0 11 3 Succulent-Karoo 5 82 135 112 8 24 15 Fynbos 6 71 266 123 16 64 30

8.5 % of the total Lepidoptera fauna. The percentage Mey, W. 2011. Basic pattern of Lepidoptera diversity in rises to 14 % in Succulent Karoo and 24 % in Fynbos southwestern Africa. Esperiana Memoir 6, 320 pp. localities.

The Geometridae of the Amanos mountains in southern Turkey – with a review of the historical exploration

Feza Can Cengiz & Axel Hausmann

Can Cengiz, F. & Hausmann, A. 2014. The Geometridae of the Amanos mountains in southern Turkey – with a review of the historical exploration. P. 263 in: Hausmann, A. (ed.). Proceedings of the eighth Forum Herbulot 2014. How to accelerate the inventory of biodiversity (Schlettau, 30 June – 4 July 2014). Spixiana 37 (2). Feza Can Cengiz (corresponding author), Mustafa Kemal University, Faculty of Agriculture, Plant Protection Dept., Entomol- ogy Section, 31034 Antakya (Hatay), Turkey; e-mail: [email protected]

The Amanos mountains in the east Mediterranean at the intersection point of three different phytogeo- Region of Turkey arise sharply from sea level up graphic vegetation zones, i. e. the Euro-Siberian, the to 2240 m (Mıgır Peak) and are situated from Kah- Irano-Turanian and the Mediterranean zone. ramanmaras to Hatay province measuring approx. The biodiversity of the Amanos mountains is 200 km in length and 25 km in width. Its topographi- notably rich as a consequence of the above men- cal, geological and geomorphological features sup- tioned geological and climatic diversity. Many ported a high rate of endemism and a large number reptiles, mammalians, freshwater fishes, butterflies of still ongoing speciation events. Therefore, the and plants were described as endemic species and Amanos mountains can be regarded as a ‘laboratory subspecies. However, there is no comprehensive and of evolution’ and thus are an ideal model for case no recent study on the moths of this mountain range. studies in research of evolution biology, biogeogra- An ongoing project will investigate the biodiversity phy and the effects of biotic and abiotic factors on of moths of the Amanos mountains, their habitats, biodiversity (e. g. effects of climatic change). The vertical and horizontal distribution, abundance, Amanos mountains are one of the least damaged host-plants and (potential) pest status by combining natural ecosystems of Turkey. The range is located morphological and molecular methods.

Contribution to an understanding of the early stages (egg, larva) of Lythria sanguinaria (Duponchel, 1842) with reference to two species in the Rhodometrini Agenjo, 1952 (Geometridae, Sterrhinae) (data from central Spain)

Gareth Edward King

King, G. E. 2014. Contribution to an understanding of the early stages (egg, larva) of Lythria sanguinaria (Duponchel, 1842) with reference to two species in the Rhodometrini Agenjo, 1952 (Geometridae, Sterrhinae) (data from central Spain). Pp. 263-264 in: Hausmann, A. (ed.). Proceedings of the eighth Forum Herbulot 2014. How to accelerate the inventory of biodiversity (Schlettau, 30 June – 4 July 2014). Spixiana 37 (2). Gareth E. King, Departamento de Biología (Zoología), Universidad Autónoma de Madrid, C / Darwin, 2, 28049 Cantoblanco (Madrid), Spain; e-mail: [email protected]

Data obtained ex females (foothills of Sistema Cen- level both in terms of morphology (L5) and resting tral, central Spain, 720m) under captive conditions position in relation to the substrate also coincides produced images of egg deposition with strategies with Rhodometra sacraria. Initial analyses of larval employed in a similar fashion to both Rhodometra chaetotaxy (L5) suggest only three SV setae on the sacraria (Linnaeus, 1767) (Skule 1980) and Casilda anterior surface of A6 pro-leg, interestingly the anal consecraria (Staudinger, 1871); images were also pro-leg (A10) places the CD2 seta below the level provided of larvae in L1 and L5. Host plant data co- of the L2 seta, a Sterrhine larval synapomorphy incide with that of Lythria cruentaria (Hufnagel, 1767) already recognised in the 1950s (Singh 1951) when which also feeds on Rumex acetosella (Polygonaceae) the Lythriini Herbulot, 1962 were still considered (Ebert & Steiner 2001). Larval habitus at a general larentiines (Õunap et al. 2008).

Ebert, G. & Steiner, A. 2001. Sterrhinae. In: Die Schmet- Singh, B. 1951. Immature stages of Indian Lepidoptera, terlinge Baden-Württembergs, Band 8: Nachfalter No. 8: Geometridae. Indian Forest Records 8 (7): VI, Geometridae. 541 pp., Stuttgart, Alemania (Ver- 67-160. lag E. Ulmer). – – 1980. Rhodometra sacraria L. Lidt om artens biologi Õunap, E., Viidalepp, J. & Saarma, U. 2008. Systematic og udbredelse, samt om den anden europaeiske position of Lythriini revised: transfered from Laren Rhodometra-art: Rhodometra anthophilaria Hb. Lepi tiinae to Sterrhinae (Lepidoptera: Geometridae). doptera, København 3 (9): 261-268. Zoologica Scripta 37: 405-413.

Unexpected feature of geometrid species composition (Lepidoptera, Geometridae) on the small islands in the Peter the Great Gulf (Sea of Japan, south of Russian Far East)

Evgeny A. Beljaev

Beljaev, E. A. 2014. Unexpected feature of geometrid species composition (Lepidoptera, Geometridae) on the small islands in the Peter the Great Gulf (Sea of Japan, south of Russian Far East). Pp. 264-266 in: Hausmann, A. (ed.). Proceedings of the eighth Forum Herbulot 2014. How to accelerate the inventory of biodiversity (Schlettau, 30 June – 4 July 2014). Spixiana 37 (2). Evgeny A. Beljaev, Institute of Biology and Soil Science, Far Eastern Branch of Russian Academy of Sciences, Sto Let Vladi vostoku str. 159, Vladivostok 690022, Russia; e-mail: [email protected]

Unexpected feature of arealogical structure of the and in 2012 on the Rikord Island (area 5.0 km2), on moths’ species assemblages on four small shelf the Bolshoi Pelis Island (area 3.1 km2) and on the islands in the Peter the Great Gulf (Sea of Japan, Furugelm Island (area 1.9 km2); also literature data south of Russian Far East) is discussed. Before the was infolded for the Askold Island (area 14.6 km2). geometrid fauna, also as nocturnal lepidopterofauna For comparison three neighbouring continental ge- as whole, on these islands was almost unknown. ometrid faunas were taken (2006, 2009). Table of spe- Details are published in Beljaev (2013). cies is published in Beljaev (2013). Statistical analysis The study was conducted according to standard was performed using the detrended correspondence entomological procedures of insect collecting and analysis (Hill & Gauch 1980). Typification of areas chorological analysis of local faunas. Materials were was made following the principles by Gorodkov, obtained during the author’s field studies in 1997 modified for geometrids by Beljaev (2011).

Table 1. Number and proportion (%) of geometrid species from different arealogical groups in local faunas in Pri- morskii region.

Arealogical group Ask. Rick. B.P. Fur. Laz. Lit. Razd. Prim. Widespread 49/34.5% 26/32.9% 18/32.7% 31/28,9% 104/33.8% 92/29.9% 96/30.6% 154/28.9% Central Palaearctic-Far Eastern 15/10.6% 4/5.1% 8/14.6% 10/9,5% 30/9.7% 21/6.8% 43/13.6% 65/12.3% East Asian 76/53.5% 44/55.7% 29/52.7% 65/60,7% 166/53.9% 190/61.7% 169/53.8% 302/56.6% Far Eastern 2/1.4% 2/2.5% 0/0% 0/0% 5/1.6% 1/0.3% 3/1.0% 5/0.9% East Asian-Indo-Malayan 0/0% 3/3.8% 0/0% 1/0,9% 3/1.0% 4/1.3% 3/1.0% 7/1.3% Total 142/100% 79/100% 55/100% 107/100% 308/100% 308/100% 314/100% 533/100% Territories: Ask., Askold Islands; Rick., Ricord Islands; B.P., Bolshoi Pelis Islands; Fur., Furugelm Islands; Laz., Lazovsky Nature Reserve; Lit., Litovka Mountain; Razd., Razdolnaya river; Prim., Primorskii region. Arealogical groups: Widespread: species with broad Palaearctic or Holarctic ranges; Central Palaearctic-Far Eastern: species with ranges covering east of Central Asia, South Siberia, Mongolia, North- East China and countries around the Sea of Japan; Far Eastern: species with ranges covering most northeastern Pacific Asia south to the lands around northern part of the Sea of Japan; East Asian: species with ranges covering the extratropical China (except west) and territories neighboring to the Sea of Japan; East Asian-Indo-Malayan: species with ranges covering subtropical and tropical zones of East, South and Southeast Asia.

Fig. 1. Major arealogical groups of geometrid moths on the islands and in the continental local faunas in Primorskii region. A. Number of species; B. proportions (%) of species. Notations see Table 1.

As a result, it was found that geometrid fauna degree of compliance of their arealogical structure demonstrates high degree of patchiness between the to neighbouring continental localities. However, this islands and species richness at times lesser than in hypothesis assumes an equivalence of distribution neighbouring continental localities. Nevertheless, a of migratory ability of moths in large arealogical high similarity of arealogical structure of the moths groups, which requires special research. inhabited the islands and the continental localities was explored (Table 1, Fig. 1). The author expresses his sincere gratitude to V. V. Ivin This is unexpected because of low species rich- and I. A. Kashin (Institute of Marine Biology of RAS, ness of geometrids on the islands and their mosaic Vladivostok) for the invitation to participate in the distribution between them, being original current study of the fauna of the island of the Peter the Great climatic conditions on the islands and their separa- Gulf, and to management and staff of the Far Eastern State Marine Biosphere Reserve for assistance in the tion from mainland at beginning of Holocene in field work. This work was partially supported by RFBR different climatic epoch (Markov 1983). grant No 14-04-00649 and grants of Presidium of Far According to the classic views of the theory of Eastern Branch of RAS No 12-I-OBN-02, No 12-I-P30-03, island biogeography, richness and composition of No 12-II-0-06-019 and No 12-III-A-06-069. biota on islands depend on the balance of rate of foreign colonization and rate of extinction of resident Beljaev, E. A. 2006. Geometrids (Lepidoptera, Geometri- populations. On the example of small islands of the dae) in rare ecosystems of the Western Primorskii Baltic Sea (the southwestern Archipelago off the coast Krai: biodiversity, chorology and ecology. A. I. of Finland) Nieminen & Hanski (1998) showed that Kurentsov’s Annual Memorial Meetings 17: 29-56 structure of population and migration of nocturnal [in Russian with English summary]. Lepidoptera on these islands meet this assumption. – – 2009. Family Geometridae. Pp. 258-271 in: Storo Besides, these authors shown the mixed nature of zhenko, S. Y. (ed.). Nasekomye Lazovskogo zapo vednika [Insects of Lazovsky Nature Reserve]. populations of moths on the small islands, included Vladivostok (Dal’nauka) [in Russian]. both resident populations and continental-island – – 2011. Fauna and chorology of geometrid moths metapopulations supported by flow of migrants (Lepidoptera, Geometridae) of the Russian Far East. from the mainland coast. Pp. 158-183 in: Lelei A. (ed.). Key to the insects Taking into account results obtained by Niemi of Russian Far East. Additional volume. Analysis nen & Hanski (1998), the agrological structure on of fauna and general reference titles. Vladivostok the small islands in the Peter the Great Gulf could (Dal’nauka) [in Russian]. be explained by assuming that the moths on the – – 2013. Features of the fauna of geometrid moths islands represented mainly by resident populations, (Lepidoptera: Geometridae) on the islands of the which occasionally, but regularly over long time Peter the Great Gulf. A. I. Kurentsov’s Annual Me- intervals, are replenished by random immigrants morial Meetings 24: 71-100 [in Russian with English summary]. http://www.biosoil.ru/kurentsov/24/ from mainland. This random immigration could xxiv-05/P-xxiv-05.pdf/ [accessed 06-Oct-2014]. alignment of arealogical structure of moths between Hill, M. O. & Gauch, H. G. 1980. Detrended correspond- islands and mainland. This model could explain both ence analysis: an improved ordination technique. a high degree of patchiness of the species composi- Vegetatio 42: 47-58. tion of the moths on the islands, as well as a high

Markov, Y. D. 1983. Shelf zone of the Sea of Japan off Nieminen, M. & Hanski, I. 1998. Metapopulations of the coast of south Primorye in Late Pleistocene moths on islands: a test of two contrasting models. and Holocene. Vladivostok (DVNTs AN SSSR) [in Journal of Animal Ecology 67: 149-160. Russian].

Charissa, subgenus Pterygnophos: little-known geometrid moths from Central Asia

Laura Marrero Palma & Sven Erlacher

Marrero Palma, L. & Erlacher, S. 2014. Charissa, subgenus Pterygnophos: little-known geometrid moths from Central Asia. P. 266 in: Hausmann, A. (ed.). Proceedings of the eighth Forum Herbulot 2014. How to accelerate the inventory of biodiversity (Schlet- tau, 30 June – 4 July 2014). Spixiana 37 (2). Sven Erlacher (corresponding author), Museum für Naturkunde, Moritzstr. 20, 09111 Chemnitz, Germany; e-mail: [email protected]

Charissa Curtis, 1826 is a species-rich genus within a subgenus of Gnophos Treitschke, 1825, but now the Ennominae. Most of them occur in the Palae- transferred to the genus Charissa. The species of that arctic region. Externally they resemble each other subgenus occur in Southeast Asia, Mongolia and due to their adaptation to rocks. Therefore they are South Siberia. There has been no revision of that generally considered to be hardly determinable. group for 60 years. As a result of the recent work For that reason it is often necessary to analyse their one species from Mongolia was considered as new. genitalia, but even then, differences between species Three species have to be transferred from Gnophos are sometimes difficult to find. Treitschke, 1825 to Charissa, and three new synonyms Within the genus Charissa Curtis, 1826 the sub- were recognized. Now the subgenus Pterygnophos genus Pterygnophos Wehrli, 1951 was taxonomically comprises four species in total which are presented revised. Pterygnophos was originally proposed as in detail.

Phylogeny and classification of Timandrini and related groups – preliminary results

Erki Õunap

Õunap, E. 2014. Phylogeny and classification of Timandrini and related groups – preliminary results. P. 266 in: Hausmann, A. (ed.). Proceedings of the eighth Forum Herbulot 2014. How to accelerate the inventory of biodiversity (Schlettau, 30 June – 4 July 2014). Spixiana 37 (2). Erki Õunap, Institute of Ecology and Earth Sciences, University of Tartu, 51014 Tartu, Estonia; and Institute of Agricultural and Environmental Sciences, Estonian University of Life Sciences, Kreutzwaldi 5, 51014 Tartu, Estonia; e-mail: [email protected]

The geometrid subfamily Sterrhinae comprises two lineage’ was revised using molecular phylogenetic clades, which informally have been named ‘Ster- approach. The results demonstrate that Timandrini rhini lineage’ and ‘Timandrini lineage’. The latter and Cosymbiini in the current sense are paraphyl- comprises the tribes Cosymbiini, Timandrini, Rho- etic. Moreover, genera Pseudosterrha Warren, 1888, dometrini and Lythriini. However, morphological Chlorerythra Warren, 1895 and Traminda Saalmüller, data indicate that placements of several genera in 1891 form a separate lineage that does not fit within these tribes may need revision. In the current study, any of the currently recognized tribes. generic composition of tribes placed into ‘Timandrini

266