Murányi, Dv J.M. Tierno de Figueroa, & M.J. López-Rodríguez. 2012. On the trophic role of Leuctra cf. signífera (Plecoptera, IK.*," Leuctridae) in a small stream in Mara valley (East Carpathians, Romania). ^P"ty' Illiesia, 8(15):147-151. Available online: http://www2.pms-lj.si/illiesia/Illiesia08-15.pdf urn:lsid:zoobank.org:pub:7C3A2A5C-AEDD-4CA0-9B66-6E22796BA17A ON THE TROPHIC ROLE OF LEUCTRA CF. SIGNIFERA (PLECOPTERA, LEUCTRIDAE) IN A SMALL STREAM IN MARA VALLEY (EAST CARPATHIANS, ROMANIA) Dávid Murányi1, José Manuel Tierno de Figueroa2 & Manuel Jesús López-Rodríguez3 1 Department of Zoology, Hungarian Natural History Museum, H-1088 Baross u. 13, Budapest, Hungary E-mail : muranyi@zool.nhmus.hu 2 Department of Zoology, University of Granada, Campus Fuentenueva s/n, 18071, Granada, Spain. E-mail: jmtdef@ugr.es 3 Department of Ecology, University of Granada, Campus Fuentenueva s/n, 18071, Granada, Spain. E-mail: manujlr@ugr.es ABSTRACT A study of the gut contents of nymphs of Leuctra cf. signífera Kempny 1899 from the Mara valley (Romania) was carried out on the basis of three samples taken in different seasons, as well as a study of the feeding habits of the 24 coexisting taxa. The diet of L. cf. signifera was composed mainly by coarse particulate organic matter (CPOM) and detritus, this species is both shredder and collector-gatherer. The macroinvertebrate community was dominated by collector-gatherers and scrapers, followed by shredders, while predators were scarce and filterers were absent. The studied community would coincide with that typical for a mid- to low-order stream. Keywords: Plecoptera, Leuctra cf. signifera, trophic ecology, CPOM, Carpathians INTRODUCTION A peculiar population of Leuctra signifera Kempny 1899, whose larval head characters include horn-shaped lateral protrusions rich of mechanoreceptors lack ommatidia (Fig. 1), has been recently recorded in Mara valley (Eastern Carpathians, Romania) (Rebora et al. 2010). With the aim to document the trophic ecology of this particular population, a study of the gut contents of the nymphs of this species was carried out. Moreover, to better understand their role in the whole macroinvertebrate community, a study of the feeding habits of the 24 taxa that coexist with this species in this stream was made. The Mara valley is a northward directed, 40 km long system between the Igni§ and Gutai Mts. These mountains are part of a ridge that diverges from the main chain of the Carpathians, gradually sloped to the Pannonian Plain westwards. This peculiar Leuctra seems to be restricted to the springbrooks of the Mara River, separated by the Pannonian Plain of about 500 km from the L. signifera populations known only from the Eastern Alps and its foothills. Other stoneflies found in the Mara springbrooks also differ from the typical forms and probably need to be described as new taxa (Muranyi 2006); these are reported herein as Gen. cf. sp. Among them, the most interesting is the Taeniopteryx cf. nebulosa population, as T. nebulosa inhabits rivers and large streams while in the Mara valley we found it in small brooks in common with typical crenal and upper rhitral species. In addition to the stoneflies, the Igni§ plateau has other microendemic water invertebrates like the Illiesia - http://www2.pms-lj.si/illiesia/ Volume 8 - Number 15 - Page 147 Murányi, Dv J.M. Tierno de Figueroa, & M.J. López-Rodríguez. 2012. On the trophic role of Leuctra cf. signífera (Plecoptera, IK.*," Leuctridae) in a small stream in Mara valley (East Carpathians, Romania). ^P"ty' Illiesia, 8(15):147-151. Available online: http://www2.pms-lj.si/illiesia/Illiesia08-15.pdf Fig. 1. Larval habitus of Leuctra cf. signifera from Mara valley. snail Bythinella molcsanyi Wagner 1941 or the caddisfly Chaetopteryx aproka Olah 2011. MATERIAL AND METHODS The studied brook is a first order unnamed tributary of the Mara, locality data: Romania, Maramureg county, Ignig Mts, Desegti-Statiunea Izvoare, on the Valhani Plateau, 1020m a.s.l., N 47°43.015' E 23°44.547'. The brook flows through an open wet meadow with Eriophorum and seeps with Sphagnum (Fig. 2). The width is approximately 0.5 m with steep banks, and depth is between 10 and 20 cm. The velocity is moderately fast, and acidic typical of the whole volcanic plateau. Despite the low elevation, climate of the plateau is rather cold and wet. The streambed consists of volcanic stones, pebbles, gravel patches and Fontinalis (Fig. 3). Semiquantitative samples were collected on 03.05.2009, 07.10.2010 and 31.03.2011: a collecting net was submerged into narrow brook sections, and an upstream area of approximately 0.5 m2 was disturbed by hand. The semiquantitative samples were enhanced by collecting single specimens of rare taxa missing from the samples but present in the stream section. The analysis of the feeding habits was carried out using the methods of Bello & Cabrera (1999) adapted to the study of the digestive tract, as has been done in other works studying stonefly and other macroinvertebrate feeding (Tierno de Figueroa et al. 2006; Lopez-Rodriguez et al. 2009). Each individual was placed into a vial with Hertwig's liquid and heated in an oven at 65 °C for approximately 24 hours, which provided a clear view of the gut contents. Afterwards, the specimens were mounted on slides for study under an Olympus CX21LED binocular optical microscope. Absolute gut content, calculated as a percentage of the gut occupied by food, was determined at 40x, and the percentage of the relative contribution of each food item to the total gut content was determined at 400x. All specimens were studied using this method except Dina sp., and due to its fluidophagous habits, did not allow a clear identification of the gut content. The diet of Dina sp. was obtained from Tachet et al. (2010). Taxa were assigned to Functional Feeding Groups (FFG; Merritt & Cummins 2006) according to the main gut contents. Illiesia - http://www2.pms-lj.si/illiesia/ Volume 8 - Number 15 - Page 148 Murányi, Dv J.M. Tierno de Figueroa, & M.J. López-Rodríguez. 2012. On the trophic role of Leuctra cf. signífera (Plecoptera, IK.*," Leuctridae) in a small stream in Mara valley (East Carpathians, Romania). ^P"ty' Illiesia, 8(15):147-151. Available online: http://www2.pms-lj.si/illiesia/Illiesia08-15.pdf Figs. 2-3. The study site: springbrook of Mara River, East Carpathians, Romania. 2: habitat; 3. substrate. RESULTS AND DISCUSSION The diet of Leuctra cf. signifera was composed of mainly coarse particulate organic matter (CPOM) and detritus (Table 1). Other minority components were fungi hyphae, spores and diatoms, but their low density in the guts would indicate that they were ingested incidentally with CPOM or detritus. Thus, this species is both shredder and collector-gatherer. This classification is consistent for the genus Leuctra (mainly collector-gatherer but also shredder and grazer; Graf et al. 2009). The macroinvertebrate community was composed of 24 taxa (sometimes identified only to generic level) belonging to eight Orders (Table 1). The most abundant taxon in the samples was Gammarus sp., followed by L. cf. signifera. Regarding their trophic role, collector-gatherers and scrapers were the dominant groups, followed by shredders. The great presence of scrapers in the community may be related to the massive growth of diatoms due to the absence of canopy and, especially, to the acidic water that outflows from the Sphagnum bogs. Predators were very scarce, only represented by Isoperla cf. sudetica and Dina sp. Nevertheless, some taxa that in this work have been recorded as non-predators because they were collected in their early developmental stages, could act as predators when older (e.g. Isoperla sp. and Rhyacophila sp.). Filterers were absent in the community. In accordance with the trophic structure, the studied community would coincide with that typical for a mid- to low-order stream (Vannote et al. 1980). Furthermore, many taxa feed on very different resources at any particular point in time, and even from different trophic levels, e.g. Isoperla cf. sudetica or Rhyacophila sp. acting as predators and collector-gatherers. REFERENCES Bello, C.L. & M.I. Cabrera. 1999. Uso de la técnica microhistológica de Cavender y Hansen en la identificación de insectos acuáticos. Boletín Entomológico Venezolano, 14:77-79. Illiesia - http://www2.pms-lj.si/illiesia/ Volume 8 - Number 15 - Page 149 Murányi, Dv J.M. Tierno de Figueroa, & M.J. López-Rodríguez. 2012. On the trophic role of Leuctra cf. signífera (Plecoptera, IK.*," Leuctridae) in a small stream in Mara valley (East Carpathians, Romania). ^P"ty' Illiesia, 8(15):147-151. Available online: http://www2.pms-lj.si/illiesia/Illiesia08-15.pdf Table 1. Gut content composition and FFG of the macroinvertebrate taxa in Mara valley. Values are Mean±SD (minimum-maximum); C-g= collector-gatherer; Sh= shredder; Sc= scrapper; P= predator; * Data from Tachet et al. (2010). Taxon N % detritus % MOPG % hyphae % spores % diatoms % pollen % prey FFG Rhitrogena iridina (Kolenati, 1839) 6 64.3±25.9 (1990) 24.2±27.1 (0-70) 8.5±4.1 (3-15) 2.2±2.7 (0-6) 0.7±1.6 (0-4) 0.2±0.4 (0-1) - C-g/Sh Rhitrogena sp. 8 10.5±2.0 (8-15) 4.0±4.2 (0-10) 5.3±3.1 (2-10) 0.5±1.4 (0-4) 79.8±6.2 (70-90) 0.0 - Sc Baetis rhodani (Pictet, 1843) 1 84.0 0.0 15.0 1.0 0.0 0.0 - C-g Baetis sp. 2 14.0±1.4 (13-15) 2.5±3.5 (0-5) 1.0±1.4 (0-2) 0.0 82.5±3.5 (80-85) 0.0 - Sc/C-g Rhabdiopteryx sp. 1 5.0 1.0 8.0 0.0 86.0 0.0 - Sc Taeniopteryx cf. nebulosa (Linnaeus, 1758) 2 46.5±27.6 (27-66) 35.0±21.2 (20-50) 15.0±7.1 (10-20) 3.0±0.0 (3-3) 0.5±0.7 (0-1) 0.0 - C-g/Sh Protonemura sp. 1 12.0 10.0 8.0 0.0 70.0 0.0 - Sc/C-g Nemoura carpathica Illies, 1963 2 50.0±70.7 (0-100) 50.0±70.7 (0-100) 0.0 0.0 0.0 0.0 - C-g/Sh Nemoura sp. 1 12.0 60.0 8.0 0.0 20.0 0.0 - Sh/Sc Leuctra cf. signifera Kempny, 1899 16 47.3±24.6 (0-77) 47.8±25.0 (20-100) 5.2±3.1 (0-10) 0.9±1.5 (0-6) 0.1±0.3 (0-1) 0.0 - Sh/C-g Leuctra cf. nigra (Olivier, 1811) 1 82.0 10.0 8.0 0.0 0.0 0.0 - C-g Isoperla cf. sudetica (Kolenati, 1860) 3 19.7±16.7 (10-39) 3.3±5.8 (0-10) 1.0±1.0 (0-2) 0.0 0.0 0.0 76.0±22.5 (50-90) P/C-g Isoperla sp. 1 10.0 10.0 0.0 0.0 80.0 0.0 - Sc Drusus sp. 8 17.9±17.7 (5-60) 20.6±27.9 (0-80) 3.9±3.7 (0-10) 0.0 57.5±37.2 (0-94) 0.1±0.4 (0-1) - Sc/Sh/C-g Other Limnephilidae 9 6.0±5.4 (0-15) 81.8±31.8 (0-100) 1.7±3.5 (0-10) 0.0 10.6±29.8 (0-90) 0.0 - Sh Rhyacophila sp. 1 5.0 0.0 1.0 0.0 94.0 0.0 9.0 Sc Goeridae (pupa) 1 - - - - - - - - Elmidae (adult) 1 100.0 0.0 0.0 0.0 0.0 0.0 - C-g Elmidae (larva) 5 10.2±21.1 (0-48) 0.0 2.2±4.4 (0-10) 0.4+0.9 (0-2) 87.2±21.1 (50-99) 0.0 - Sc Chironomidae 1 85.0 10.0 5.0 0.0 0.0 0.0 - C-g Niphargus puteanus baloghi Dudich, 1940 4 34.3±17.1 (13-50) 54.0±10.7 (48-70) 1.3±1.5 (0-3) 1.0±1.1 (0-2) 0.3±0.5 (0-1) 0.0 - Sh/C-g Gammarus sp. 42 50.1±20.7 (10-94) 43.9±21.3 (4-90) 5.6±3.7 (0-15) 0.3±0.9 (0-5) <0.1±0.3 (0-2) 0.0 - C-g/Sh Tubificidae 3 25.3±17.9 (15-46) 60.0±26.5 (30-80) 10.3±7.5 (3-18) 1.7±2.1 (0-4) 1.3±0.6 (1-2) 1.3±2.3 (0-4) - Sh/C-g Dina sp. 8 - - - - - - - P* Graf, W., A. Lorenz, J.M. Tierno de Figueroa, S. Lücke, M.J. Lopez-Rodriguez, & C. Davies. 2009. Distribution and Ecological Preferences of European Freshwater Organisms. Volume 2: Plecoptera. Series Editors: A. Schmidt-Kloiber & D. Hering. PENSOFT Publishers, Sofia. Kempny, P. 1899. Zur kenntniss der Plecopteren. II. Neue und ungenügend bekannte Leuctra-Arten. III. Theile. Verhandlungen der ZoologischBotanischen Gesellschaft in Wien, 49:269-278. Lopez-Rodriguez, M.J., J.M. Tierno de Figueroa, & J. Alba-Tercedor. 2009. Life history of two burrowing aquatic insects in Southern Europe: Leuctra geniculata (Insecta: Plecoptera) and Ephemera danica (Insecta: Ephemeroptera). Aquatic Insects, 31 (2):99-110. Merritt, R.W. & K.W. Cummins. 2006. Trophic relationships. pp. 585-610. In Hauer, F.R. & G.A. Lamberti [eds.]. Methods in Stream Ecology. 2nd ed. Academic Press, Inc., San Diego, CA, 877 pp. Muranyi, D. 2006. Review and contribution to the Plecoptera fauna of Maramureg, Romania. Studia Universitatis Vasile Goldig Arad, 17:85-94. Olah, J. 2011. A new species of Chaetopteryx (Trichoptera, Limnephilidae) from the Northeast Carpathians. Braueria, 38:9-10. Rebora, M., D. Muranyi, S. Piersanti & E. Gaino. 2010. The lateral protrusions of the head of the stonefly larva Leuctra cf. signifera (Plecoptera: Leuctridae). Aquatic Insects, 32 (4):259-264. Tachet, H., P. Richoux, M. Bournaud & P. Usseglio-Polatera. 2010. Invertébrés d'eau douce. Illiesia - http://www2.pms-lj.si/illiesia/ Volume 8 - Number 15 - Page 150 Murányi, Dv J.M. Tierno de Figueroa, & M.J. López-Rodríguez. 2012. On the trophic role of Leuctra cf. signífera (Plecoptera, IK.*," Leuctridae) in a small stream in Mara valley (East Carpathians, Romania). ^P"ty' Illiesia, 8(15):147-151. Available online: http://www2.pms-lj.si/illiesia/Illiesia08-15.pdf Systématique, biologie, écologie. CNRS Editions, Paris. Tierno de Figueroa, J.M., A. Vera, & M.J. Löpez-Rodriguez. 2006. Adult and nymphal feeding in the stonefly species Antarctoperla michaelseni and Limnoperla jaffueli from Central Chile (Plecoptera: Gripopterygidae). Entomologia Generalis, 29 (1):39-45. Vannote, R.L., G.W. Minshall, K.W. Cummins, J.R. Sedell, & C.E. Cushing. 1980. The river continuum concept. Canadian Journal of Fisheries and Aquatic Science, 37:130-137. Wagner, J. 1941. A Gutin-hegység Mollusca faunajanak alapvetése. Allattani Kôzlemények, 38:197-210. Received 9 August 2012, Accepted 11 September 2012, Published 1 October 2012 Illiesia - http://www2.pms-lj.si/illiesia/ Volume 8 - Number 15 - Page 151