Meligethes matronalis Audisio & Spornraft, 1990
publication ID |
https://doi.org/10.5281/zenodo.173302 |
DOI |
https://doi.org/10.5281/zenodo.5659718 |
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scientific name |
Meligethes matronalis Audisio & Spornraft, 1990 |
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Meligethes matronalis Audisio & Spornraft, 1990
( Figs. 4 View FIGURES 1 – 4 , 9–10 View FIGURES 5 – 12 , 15 View FIGURES 13 – 16 )
Diagnosis
Mediumsized (length 2.20–3.10 mm) and moderately variable species, usually dark brown with pale brown to orangebrown legs and antennae, with maximum pronotal width at posterior angles ( Fig. 4 View FIGURES 1 – 4 ). Similar to the widespread European M. subaeneus Sturm, 1845 , but with dorsal punctures denser and coarser (less close than in M. epeirosi n.sp.; spaces between punctures 1.2–1.3X diameter), body larger (2.2–3.1 mm in M. matronalis , 1.7–2.8 mm in M. subaeneus ), shiny surface between elytral punctures, pronotum less dull, and different median lobe of aedeagus being longer than M. subaeneus ( Fig. 10 View FIGURES 5 – 12 ; ratio LEAE/WIAE [ Fig. 17 View FIGURE 17 f] = 1.95–2.13 in M. matronalis , 1.66–1.78 in M. subaeneus ), and subparallel at sides (in M. epeirosi n.sp. median lobe with maximum width at distal threefifths, distinctly narrowed both distad and proximad: Figs. 11–12 View FIGURES 5 – 12 ). Quite distinct from all members of the M. coracinus subgroup due to pronotal maximum width close to the posterior angles. Female ovipositor as figured ( Fig. 15 View FIGURES 13 – 16 ), with slightly darker apex.
Geographic distribution
This species is widespread from N Spain (Pyrenean Mts.) westward throughout most of Europe, reaching the Caucasus ( Azerbaijan) eastward ( Audisio, 1993; Audisio et al., 2000, 2005a). This species is rare and local, except for localities from central and northern Europe (southern Germany to southern Finland and Sweden northward), where the presentday distribution is associated with a recent anthropogenic introduction of the larval hostplant (see below) that is widely used as an ornamental (Jalaas & Suominen, 1994; Meybohm, 1995; Renner, 1995; Spornraft, 1998; Ericson, 1999; Schillhammer & Schuh, 2004).
subgroup.
Continued species of the Meligethes coracinus subgroup (see Fig. 17 View FIGURE 17 ).
measurement measurement description
acronyms
Fig 17 View FIGURE 17 a WPR1 pronotal width at posterior angles
WPR2 pronotal width at 1/3 of its length
LEPR pronotal length
LELY elytral length (mean)
WELY elytral width (mean)
Fig 17 View FIGURE 17 b W03J maximum width of 3rd antennal joint
W10J maximum width of 10th antennal joint
Fig 17 View FIGURE 17 c LETI length of front tibiae (mean)
WITI maximum width of front tibiae, excluding teeth (mean)
Fig 17 View FIGURE 17 d LFTA total length of front tarsi (mean)
WFTA maximum width of second tarsal joint of front tarsi (mean)
LLTJ length of last tarsal joint of front tarsi (mean)
WLTJ maximum width of last tarsal joint of front tarsi (mean)
Fig 17 View FIGURE 17 e WITE maximum width of tegmen
WIMN width of tegmen at subproximal narrowest point
ANGT measure (expressed as ratio of the angular value in degrees x 100 over the value of 180°) of the sector defined by the inner edge of the paramera
LETE length of tegmen
DETE depth of tegminal incisure
Fig 17 View FIGURE 17 f LEAE length of median lobe of the aedeagus
LEOS length of the distance between the posterior edge of the aedeagal ejaculatory ostium and apex of the median lobe of the aedeagus
WIAE maximum width of median lobe of the aedeagus
Fig 17 View FIGURE 17 g V length of segment AB (apex of the median lobe of aedeagus)
H length of segment AC (apex of the median lobe of aedeagus)
Biological notes
This species is strictly monophagous, and the wellknown larval hostplant is Hesperis matronalis L. ( Brassicaceae Hesperideae ; Audisio & Spornraft, 1990; Audisio, 1993; Audisio et al., 2001a, 2002). Only a few Caucasian localities ( Armenia, Eastern Turkey) had populations associated with Hesperis transcaucasica Tzvelev (unpublished data); however this probably represents a subspecies of H. matronalis ( Davis, 1965) . Meligethes matronalis , at least in natural environments, is strongly associated with edges and clearings of broadleaved woods (beech, mesophilous oaks, alders, chestnuts, and others), from 200 to 2500 m a.s.l.
Taxonomic observations
This species, except for variation in body size (2.2–3.1 mm), appears to be morphologically homogeneous throughout most of its geographic range (both primary and secondary), except the Caucasian populations are represented by specimens showing relatively duller spaces between dorsal punctures in comparison with W. European specimens. Genetic data available from allozyme analyses ( De Biase, 2000; Audisio et al., 2002), COI gene sequences (unpublished data), and mitochondrial Control Region fragments (unpublished data), indicate a stronger genetic affinity between M. matronalis and M. coracinus , than to M. subaeneus . Despite this genetic evidence, M. subaeneus and M. matronalis are much more closely related to each other in a phenetic space described by morphometric variables ( Audisio et al., 2001a), and Kirejtshuk (1997) erroneously concluded that these two species were synonymous.
Audisio, P. & Spornraft, K. (1990) Taxonomie, Okologie und Verbreitung von Meligethes coracinus auctt. mit Beschreibung einer neuen Art (Coleoptera: Nitidulidae). Nachrichtenblatt der Bayerischen Entomologen, 39, 70 - 75.
Audisio, P. (1993) Coleoptera Nitidulidae-Kateretidae. Fauna d'Italia, 32. Calderini Editore, Bologna, XVI + 971 pp.
Audisio, P., Jelinek, J., Mariotti, A. & De Biase, A. (2000) The Coleoptera Nitidulidae and Kateretidae from Anatolian, Caucasian and Middle East regions. Biogeographia, Lavori della Societa italiana di Biogeografia, 21, 241 - 354.
Audisio, P., Belfiore, C., De Biase, A. & Antonini, G. (2001 a) Identification of Meligethes matronalis Audisio and Spornraft, 1990 and M. subaeneus Sturm, 1845, based on morphometric and bionomic characters (Coleoptera: Nitidulidae). European Journal of Entomology, 98, 87 - 97.
Audisio, P., De Biase, A., Antonini, G., Oliverio, M., Ketmaier, V. & De Matthaeis, E. (2002) Specific distinction by allozymic data of sympatric sibling species of the pollen-beetle genus Meligethes (Coleoptera: Nitidulidae). Italian Journal of Zoology, 69, 65 - 69.
Audisio, P., De Biase, A., Antonini, G., Mancini, E., Ozbek, H. & Gultekin, L. (2005 a) Redescription and natural history of Meligethes longulus Schilsky, 1894, and provisional revision of the M. coracinus species-complex (Coleoptera, Nitidulidae, Meligethinae). Italian Journal of Zoology, 72, 73 - 85.
Davis, P. H. (1965) (ed.) Flora of Turkey and the East Aegean Islands, 1. Edimburgh Univ. Press, 567 pp.
Ericson, B. (1999) Nya fynd av rapsbaggar (Coleoptera: Nitidulidae: Meligethes) med tre for Sverige nya arter. Entomologisk Tidskrift, 120, 117 - 125.
Kirejtshuk, A. G. (1997) New Palaearctic nitidulid beetles, with notes on synonymy and systematic position of some species (Coleoptera: Nitidulidae). Zoosystematica Rossica, 6, 255 - 268.
Meybohm, H. (1995) Meldungen zur Kaferfauna von Schleswig-Holstein, Hamburg und Nord- Niedersachsen. II. Teil. Bombus (Hamburg), 3, 49 - 50.
Renner, K. (1995) Meligethes reitteri Schilsky und Meligethes matronalis Audisio & Spornraft im westlichen Deutschland (Col., Nitidulidae). Mitteilungen der Arbeitsgemeinschaft Rheinischer Koleopterologen (Bonn), 5, 195 - 197.
Schillhammer, H. & Schuh, R. (2004) Bemerkenswerte Kaferfunde aus Osterreich (XII) (Coleoptera). Koleopterologische Rundschau, 74, 443 - 445.
Spornraft, K. (1998) Familie Nitidulidae, pp. 240 - 243, In: Lucht, W. & Klausnitzer, B. (Eds.): Die Kafer Mitteleuropas, 4. Supplementband. Goecke & Evers, Krefeld, 398 pp.
Jalas, J. & Suominen, J. 1994 (Eds) Cruciferae (Sisymbrium to Aubrieta). Atlas Florae Europeae, 10. University Press, Helsinki, 224 pp.
FIGURE 17. Schematic drawings of morphological characters measurements for Meligethes species—a: body shape and pronotum; b: antennae; c: protibiae; d: protarsi; e: tegmen; f: aedeagus; g: aedeagal apex. Refer to Table 2 for list of characters and acronyms.
FIGURES 1 – 4. Dorsal habitus of Meligethes epeirosi n. sp. (♂ paratype from Greece, Katara Pass, Fig. 1), of M. subaeneus Sturm (♂ specimen from Italy, Latium, Rocca di Papa, Fig. 2; ♂ specimen from Spain, Cantabria, Campollo, Fig. 3), and of M. matronalis Audisio & Spornraft (♂ specimen from Italy, Latium, Rocca di Papa, Fig. 4). Scale bar = 2.00 mm.
FIGURES 5 – 12. Tegmen and median lobe of aedeagus (dorsal view) of Meligethes coracinus Sturm (♂ specimen from Italy, Lombardia, Lovero Valtellino, Figs. 5 – 6), of M. subaeneus Sturm (♂ specimen from Italy, Latium, Rocca di Papa, Figs. 7 – 8), of M. matronalis Audisio & Spornraft (♂ specimen from Italy, Latium, Rocca di Papa, Figs. 9 – 10) and of Meligethes epeirosi n. sp. (♂ paratype from Greece, Katara Pass, Figs. 11 – 12). Scale bar = 0.50 mm.
FIGURES 13 – 16. Ovipositor of Meligethes coracinus Sturm (Ψ specimen from Italy, Lombardia, San Giacomo di Teglio, Fig. 13), of M. subaeneus Sturm (Ψ specimen from Italy, Latium, Rocca di Papa, Fig. 14), of M. matronalis Audisio & Spornraft (Ψ specimen from Italy, Latium, Rocca di Papa, Fig. 15) and of Meligethes epeirosi n. sp. (Ψ specimen from Greece, Katara Pass, Fig. 16). Scale bar = 0.50 mm.
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