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Diptera: Chironomidae): the Brackish Water Populations of Tvärminne Area, Finland

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Diptera: Chironomidae): the Brackish Water Populations of Tvärminne Area, Finland © Entomologica Fennica. 8 December 2006 Contributions to the taxonomy and ecology of the Chironomus plumosus sibling species aggregate (Diptera: Chironomidae): the brackish water populations of Tvärminne area, Finland Mauri Hirvenoja Hirvenoja, M. 2006: Contributions to the taxonomy and ecology of the Chiro- nomus plumosus sibling species aggregate (Diptera: Chironomidae): the brack- ish water populations of Tvärminne area, Finland — Entomol. Fennica 17: 373– 380. Based on pupal exuviae, two sympatric pupal forms of Chironomus plumosus auctt. are present in the museum materials collected in 1952–1962 from the brackish water near the Tvärminne Biological Station at the northern Baltic Sea. The predominating undescribed type of the pupal exuviae is called here the “Bal- tic marine species” (possible C. plumosus sensu Linnaeus; direct observations by Linnaeus of Tipula plumosa from freshwater are not on record). Its pupal exuviae and the associated female and male from the Tvärminne population are de- scribed. Attempts to find larvae of the genus Chironomus in the sea area of Tvärminne for the renewed and more complete studies failed during the 1980s and 1990s. Only two larvae of the undescribed species of the karyological Chiro- nomus plumosus group were captured. The possible reasons for the supposedly changed environmental conditions are discussed. M. Hirvenoja, Sotilaskorventie 13, FI-01730 Vantaa, Finland Received 20 January 2004, accepted 22 November 2005 1. Introduction each other. The BR (beard ratio) value (Strenzke 1959) of the adult male fore tarsi is high. The pu- Over ten defined sibling species have been de- pal exuviae have patches of about 10 µm long and scribed in a group which should include, among proximally 1–2 µm thick spinules in the anal cor- others, Chironomus plumosus (Linnaeus), some ners of segments 5–7, which are a little strength- only on the basis of the larval karyology. Many of ened obviously synapomorphously, whereas them may be sympatric, but the morphological paratergites 5–8 are smooth as in some other spe- determination in different sites may be difficult cies of this genus. e.g. because of intraspecific variation. In the list This combination of characters appears to be of Michailova (2001) there are three species that present also in the pupae of C. nuditarsis Keyl, have been karyologically recorded from Finland. the males of which are easily separable from the In the morphological sibling species aggre- species of the aggregate discussed here by the gate of Chironomus plumosus (as treated in the short BR value. Also the pupae of the more present paper), the pale adults are quite similar to plesiomorphous species C. coaetaneus Hirvenoja 374 Hirvenoja • ENTOMOL. FENNICA Vol. 17 (that has a very dark adult) are quite similar with himself), and two more unlabeled pins filed under the species of the aggregate. Tipula plumosa Linnaeus. Unfortunately, no pub- Taxonomical differentiation of sibling species lications (observations or interpretations) of this is important in the biological monitoring of the material are known. As long as the above-men- environment. If no separation is achieved, the un- tioned probable type material has not been evalu- resolved “collective species” can appear as ubiq- ated, the name Chironomus plumosus (Linnaeus) uitous, which significantly reduces the relevance cannot be used or diagnosed against with any cer- of such studies. A great mass of limnological in- tainty. formation has been published under the name This also concerns the relations between the Chironomus plumosus (L.), unfortunately often karyologically described species and the numer- at a taxonomic level that precludes referring to ous synonyms of C. plumosus given e.g. by Goet- such data with confidence. ghebuer (1937–1954), because type materials for It is not necessary to use terms such as the some names are present in various museum col- “plumosus group”, “plumosus type” larvae (ven- lections (Coll. Meigen, Paris; Coll. Zetterstedt, tral tubules at least as long as the corresponding Lund). segment, lateral tubules of segment 7 present), or The pupal exuviae of C. plumosus sensu “semireductus type”, etc., and they should be dis- Strenzke (1959) and Keyl & Keyl (1959) have continued. This is especially true for the last- been described by Langton (1991, 1995; cf. Sho- mentioned name, because “semireductus” is not banov 2003). This species, which should have an available scientific name for a species or sub- smooth 3rd and 4th abdominal sternites, has been species. Thienemann (1954: 135–143) discusses karyologically observed especially in several earlier studies with particular emphasis on the fresh water habitats in Europe. On the basis of the length of the tubules being species-specific but karyology, the same species has also been re- depending on the oxygen content of the milieu. ported from lakes in Finland [Sodankylä: Lokka However, according to Shobanov (1989: 336), reservoir, Inkoo: Marssjön, Lohja: Lohjanjärvi, there is intraspecific variability in the length of Anttola: Paljavesi, Savonlinna: Pihlajavesi (Mi- the tubules. chailova 2001, Michailova & Mettinen 2000) and one minor variety of exuviae from Lokka, sub Chironomus pr. plumosus Linnaeus illustrated in 2. Tipula plumosa Linnaeus (1758) Hirvenoja (1998)]. On the basis of the pupal exuviae, this com- Tipula plumosa Linnaeus (1758) was first ob- mon “lacustrine species” (C. plumosus auctt.) oc- served on and near Öland, Sweden and near Käm- curred like many other freshwater chironomid pinge on the southern Swedish coast [Linnaeus species in the shallow brackish waters (salinity up (1745), translated by Åsberg & Stearn (1973); to 6E/4) of the Baltic Sea at Tvärminne (Palmén Linnaeus (1746, 1751, 1758, 1761)]. According 1955, Palmén & Aho 1966). Kerkis et al. (1989) to Linnaeus’ descriptions the larvae were living used larval karyology and showed a species un- mostly in the sea [Linnaeus (1746, 1761): “Habi- der the name C. plumosus to occur in Kurshsk tat hujus Larva in mari”; Linnaeus (1758): “Habi- Bay, Lithuania, where the salinity according to tat in Europa, imprimis in maritimis”]. The quali- Järvekülg (1979) is 5–6E/4. The pupal exuviae of fier “imprimis” (mostly) in the latter statement the last mentioned population are unknown. probably accommodates the descriptions of spec- In the collection of the Finnish Museum of imens from inland waters by other authors (e.g. Natural History, Helsinki, there is one vial con- Goedart, Réaumur), which Linnaeus cited and taining pupal exuviae similar to that of the most thought to denote the same species. Direct obser- common “lacustrine plumosus”(C. plumosus vations by Linnaeus of T. plumosa from freshwa- auctt.) from the shallow alfa-mesohaline (salinity ter are not on record. <2E/4) Gennarbyviken Bay of the Baltic Sea, not The Linnaean insect collections at the Lin- far from Tvärminne, collected in July, 1957 by nean Society of London reportedly contain one Dr. K. Purasjoki. In exuviae of a single pupa of pin-labeled “plumosa” (supposedly by Linnaeus this sample, traces of spinulation on sternite 3 are ENTOMOL. FENNICA Vol. 17 • Chironomus plumosus of the Baltic Sea 375 Fig. 1. Chironomus plumosus sibling species aggregate; scale bar 100 µm. – a. Variation of the spinulation of ab- dominal sternites (a), parasternites (a) and paratergites (a1) schematically in the pupal exuviae of the “lacustrine form”. The left side in (a) = the shagreen of an “intermediate individual” from Gennarbyviken. – b–d. Details of the “Baltic marine species” from Tvärminne. Spinulation of the sternites (b), parasternites (b) and paratergites (b1), posterior thoracic tracheal bladder (c), male hypopygium (d), spermatheca and the bilobed subgenitalplate of segment 8 in female. 376 Hirvenoja • ENTOMOL. FENNICA Vol. 17 also present (Fig. 1a), but the pleural points of 2.1. Description of the material segment 4 are absent as is usual in the `lacustrine from the Tvärminne sea area plumosus’ of the other populations known from the Finnish lakes. Palmén & Aho (1966) reported the distribution In the population of the Lake Marssjön, and emergence of a population under the name Inkoo, ca. 2 km from the coast of the Gulf of Fin- Chironomus plumosus L. (coll.) in the northern land, however, the pleural points of segment 4 are Baltic Sea around the Tvärminne Biological Sta- very distinct as in the “Baltic marine species”. tion. From their measurements of 20 male speci- Karyologically (Michailova 2001) the latter po- mens, the authors concluded that the material pulation should also be C. plumosus auctt.,i.e.the captured in Tvärminne agrees quite well with the species called “lacustrine plumosus’ here. redescription of this species from the fresh waters In the literature, there are at least two more of Holstein, Germany by Strenzke (1959). The karyological species in the C. plumosus aggre- populations from Holstein were karyologically gate with smooth sternites 3 and 4 (based on ma- studied by Keyl & Keyl (1959). However, al- terial in coll. P. Michailova), namely C. bonus though the karyology was not studied in Tvär- Shilova & Dyvarsheishvili and C. vancouveri minne, the difficulties associated with the taxon- Michailova & Fischer. These have not been found omy were already well known at that time. This is in Finland. In contrast to the most European lac- why the species name was somewhat questioned, ustrine populations, the pupae in the original ma- as indicated by the expression “(coll.)”. terial of the latter species have
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