Weevil News |
http://www.curci.de/Inhalt.html |
No.6. |
10 pp. |
21 October 2001 |
ISSN 1615-3472 |
Knutelski, S. (2001): Cryptorhynchinae weevils
(Coleoptera: Curculionidae) of the Tatra Mountains. Contributions to the
weevil fauna of the Tatra Mountains. |
|||||
Weevil News: http://www.curci.de/Inhalt.html,
No. 6: 10 pp., CURCULIO-Institut: Mönchengladbach. (ISSN 1615-3472). |
Cryptorhynchinae weevils (Coleoptera: Curculionidae)
of the Tatra Mountains. Contributions to the
weevil fauna of the Tatra Mountains
By S t a n i s ł a w K N U T E L S K I
with 41 figures
Abstract
Data on the distribution of five weevil species (Cryptorhynchus
lapathi, Acalles camelus, A. commutatus, Onyxacalles croaticus, O. pyrenaeus)
of the subfamily Cryptorhynchinae (Coleoptera: Curculionidae) occurring in
the Tatra Mountains with all collecting data are given. A. commutatus is
recorded for the first time for the Tatra Mountains, and 4 other species are
new (*) for the fauna of the particular region of the Tatra Mountains. Finally,
all faunistical data on the remarkable species of the Tatra Mountains are shown
and discussed.
Key words: Faunistics, distribution, ecology,
mountains of Europe, Carpathians, Poland, Slovakia, Coleoptera, Curculionidae,
Cryptorhynchinae, Cryptorhynchus, Acalles, Onyxacalles.
Introduction
Between the Alps and Caucasus, the
Tatra [Fig. 1] are the highest mountains in central Europe [Fig. 2]. This mountain massif forms a natural geographical and
ecological barrier and has played an important role for the distribution of the
insect fauna in Europe during the past epochs of Quaternary and recently.
The weevil fauna of the Tatra Mountains, and
especially the Cryptorhynchinae subfamily is not well known. Up from starting
of my faunistical researches in 1985, only two species were known: Cryptorhynchus
lapathi and Onyxacalles pyrenaeus from the Tatra Mountains [M. Łomnicki
1866, 1868] [Smreczyński 1932] [Endrödi 1961]. Not long ago I recorded
[Knutelski 1988] [Knutelski & Knutelska 1998] two further species:
O. croaticus and Acalles camelus from this mountain massif.
In this paper I summarize all my faunistical data on
Cryptorhynchinae weevils from the Tatra Mountains. For some of the weevils
there is a big number of new records, and A. commutatus is recorded for
the first time from this mountain massif.
The Tatra Mountains (49oN,
20oE) form the highest range in the Carpathians [Fig. 2] [Fig. 3] at northern territory of Slovakia and the
southern part of Poland [Fig. 1]. The highest summit is Gierlach (2663 m
above sea level) in Slovakian territory, and Rysy (2499 m a.s.l.) in Poland. Length
W-E: 53 km, length of the main ridge: about 80 km; width S-N: 18,5 km. The
Tatra Mountains are covering a comparatively small area of 750 km2,
but show typical features of an alpine massif [Fig. 6]. The
majority of the area belongs to Slovakian territory, in Poland there is only 24
% of the Tatra area and all belonging to the Tatra National Park. On Slovakian
side also the majority of area of the Tatra Mountains is protected by law as
the Tatranský narodný park. From 1993 the Tatra Mountains are mentioned by
international organizations of wild-nature conservation as the Nature Reserve
“Tatra”.
The Tatra Mountains form three
principal, distinct geobotanical subdistricts (regions): Western Tatra [Fig. 5] [Fig. 12] (in Polish and Slovakian territory), to
2248 m of altitude, on the base of sedimentary and crystalline rocks; High
Tatra [Fig. 6] [Fig. 7] [Fig. 18] (in Polish and Slovakian territory), -
2663 m, crystalline and sedimentary rocks; Belianske Tatra [Fig. 8] [Fig. 9] (only in Slovakian territory), - 2151 m,
sedimentary rocks.
Crystalline rocks [Fig. 7]
(granites, gneisses, mylonites, crystalline slates) are of Paleozoic age, and
sedimentary rocks [Fig. 9] (limestones, dolomites, marls, shales,
sandstones and breccias) of Mesozoic age.
The major relief-features are of Tertiary age (two
planation surfaces and a system of valleys coinciding with the primary
inclinations and the geologic structure, which dates from that time). These
relief features were significantly changed during the Pleistocene, due to
glacial and periglacial processes, and slightly modified during Holocene.
The climate is mountainous of the
temperate zone, prevalent winds come from NW and W, also local warm foen-like
winds called “halny”, from S to N, +- 60 m/s.
Considerable differentiations of
climatic conditions along the altitudinal gradient, pronounced relief, varied
geological substrata, soils, and the geomorphological character contribute to a
great range of habitats. Together these characteristics result in great
diversity and distinctness of the flora and of plant communities. The Tatra
Mountains are divided into five bioclimatic belts: 1 - lower montane belt (near
900 to 1250 m a.s.l.) [Fig. 10] [Fig. 11], 2 - upper montane belt [Fig. 13] (1250-1500 m), 3 - dwarf pine belt (= subalpine belt)
(1500-1780 m), 4 - alpine belt (1780-2350 m), subnival belt (above to summits) [Fig. 7].
Flora and vegetation [Fig. 10] [Fig. 13] [Fig. 14] [Fig. 15] [Fig. 17] [Fig. 19] [Fig. 21] [Fig. 22] [Fig. 23] of the Tatra were strongly influenced during the
Pleistocene and were significantly changed during the Holocene. The present
plant cover and fauna have been strongly influenced and changed by historical
and contemporary human activities (wasteful forest exploitation connected with
development of settlements, pasturage, mining and metallurgy, various types of
tourism and long-distance influences). For more detailed information on
geology, geomorphology, climate and plant cover of the Tatra Mountains see:
Browicz & Zarzycki [1987], Mirek Piękoś-Mirkowa [1992],
Pawłowski [1972] and Szafer [1962].
Methods
During the field study on weevils in the whole area of
the Tatra Mountains in 1985-1999, about 28 000 specimens were collected, and
among them 23 643 were caught by the author. Only 74 specimens of the
Cryptorhynchinae subfamily were identified in this material. The
Cryptorhynchinae weevils were collected [Fig. 16] at 30
localities in the Tatra Mountains. [Fig. 30] [Fig. 31] [Fig. 32] [Fig. 33] [Fig. 34] [Fig. 35]. Six further specimens were identified in museum
collections. All collecting data and ecological informations are summarized and
most of published data were added (if necessary), resulting in a current
Cryptorhynchinae fauna of the Tatra Mountains. The taxonomic nomenclature used
here is that of Stüben [1999]; synonyms of the Tatra’s weevils were given too.
New records for the remarkable regions of the Tatra Mountains are indicated by
an asterisk (*). For weevils preserved in the museums referred to in the text,
the following acronyms are used:
MIZ - Museum
& Institute of Zoology, Polish Academy of Science, Warszawa (Poland).
ISAE -
Institute of Systematic & Animal Evolution, Polish Academy of Science,
Kraków (Poland).
SNMB - Slovak
National Museum, Bratislava (Slovakia).
In the text I used also some symbols and
abbreviations: SK - S. Knutelski; BT - Belianske Tatra region, SWT - Western
Tatra region in Slovakian territory, SHT - High Tatra region in Slovakian
territory, PWT - Western Tatra region in Polish territory, PHT - High Tatra
region in Polish territory, * -
recorded for the first time; a.s.l. - above sea level; val. - valley; loc.-
locality; ex. or exx. - exemplar or exemplares.
Results
Cryptorhynchus
lapathi (Linnaeus, 1758) [Fig. 24]
C. lapathi L.: Nowicki (1873).
*PHT [Fig. 6] [Fig. 18]: Wodogrzmoty Mickiewicza [Fig. 30],
1906/6/28, 1 ex. in the cutting forest near road, leg. S. Stobiecki, coll. ISAE, and 1951/5/21, 1 ex., leg. M. Węgrzecki, coll. MIZ, det. SK.
*PWT [Fig. 5] [Fig. 13]: Kuźnice [Fig. 30], 1897/7/6, 1 ex., in the cutting coniferous forest,
leg. S. Stobiecki, coll. ISAE, det. SK.
C. lapathi is recorded for
the first time from the regions of the High and Western Tatras regions. This
species was recorded or quoted many times before from the Tatras massif as a
whole, but generally without data on localities [M. Łomnicki 1866, 1868]
[Nowicki 1873] [Petryszak 1982] [Knutelski & Skalski 1993] [Burakowski et
al. 1995].
C. lapathi is very rare in
the Tatra Mountains and occurs only in wet habitats in some valleys at the base
of the massif where it reaches the upper limit of its vertical distribution.
This palearctic weevil colonized the whole area of
Poland without Góry Świętokrzyskie Mts., Western and Eastern Sudetes
[Burakowski at al. 1995].
Acalles camelus (Fabricius, 1792) [Fig. 25]
BT [Fig. 8]:
Tatranska Kotlina - Sumivy pramen [Fig. 31], 860-910 m a.s.l., 1991/9/14, 1 ex. in
beech forest (Dentario glandulosae-Fagetum association) from the floor
plants using an entomological sweep net, leg., det. and coll. SK.
This locality has just been quoted
by Knutelski & Knutelska [1998].
*SWT: Kycera [Fig. 31], 830-891 m a.s.l., 1993/9/14, 2 exx. in the brushwood
of the montane xerothermophilous zone, one of the individuals was collected
using a sweep net, and a second one was sieved from the litter under Thymus
sp., small spruces (Picea abies (L.) Karst.), asps (Populus tremula L.),
birches (Betula pendula Roth), large-leaved willows (Salix caprea L.),
Dianthus sp. and Centaurea sp.; Sucha val. (= Sucha dolina) [Fig. 31], 800 m a.s.l., 1993/9/14, 1 ex. in the brushwood of
Carpathians alder (Alnetum incanae association) was sieved from the
litter under alders (Alnus glutinosa (L.) Gaertn.), spruces, ashes (Fraxinus
excelsior L.), hazels (Corylus avellana L.), dogwoods (Cornus
sanguinea L.), lilacs (Syringa vulgaris L.) and large-leaf willows,
leg., det. and coll. SK.
Acalles camelus is recorded for the first time from the Western Tatra
region. It was discovered in the Tatra Mountains for the first time not long
ago [Knutelski & Knutelska 1998], and is known only from the southern
Slovakian slopes of the massif where it reaches 910 m of altitude. It is often
found also in beech forests (Dentario
glandulosae-Fagetum association) and mixed coniferous-deciduous forest at
the lower montane belt in the Tatra Mountains [Fig. 17] [Fig. 37] [Fig.
38] [Fig. 39].
This species is distributed in
Europe from Italy and Yugoslavia to France and central European countries and
to Denmark and southern Sweden [Burakowski at al. 1995].
*Acalles
commutatus Dieckmann, 1982
[Fig. 26]
*BT [Fig. 8]:
Javorina [Fig. 32] 1938/7/3, 3 exx., leg. J. Roubal, coll. SNMB, det.
SK.
*SWT: Bobrovecka vapenica [Fig. 32], 945-980 m a.s.l., 1997/8/16, 1 ex. in the brushwood
of the montane xerothermophilous zone with isolated spruces and willows was
sieved from the litter; Podnestrova [Fig. 32], 820-860 m a.s.l, 1997/8/16, 1 ex. in
herbaceous plants near the stream sieved from the litter [Fig. 37]; Sucha val. [Fig. 32], 800 m a.s.l., 1993/9/14, 1 ex. in
the brushwood of alder (Alnetum
incanae association) was sieved from the litter under alder, spruce, ash,
hazel, dogwood, lilac and large-leaf willow, leg., det. and coll. SK.
A. commutatus is recorded for the first time to the Tatra massif as
a whole, and it is new for the weevil fauna of the
Belianske Tatra and Western Tatra regions belonging to the Slovakian territory.
In the Tatra Mountains the upper limit of this weevil is 980 m a.s.l.
This species
was described not long ago [Dieckmann 1982], and is known recently from the
eastern parts of the Pyrenees (France), Lombardia and Istria (Italy), Bosnia,
Germany, Poland, Moravia (Czech Republic), Slovakia and European part of Turkey
[Burakowski at al. 1995].
Onyxacalles
croaticus (H. Brisout de
Barneville, 1867) [Fig. 27] [Fig. 28]
Acalles croaticus BRIS.: Knutelski [1988,
1991, 1993], Knutelski & Skalski [1993], Petryszak
[1993], Dieckmann & Behne [1994],
Burakowski et al. [1995].
BT
[Fig. 8]: Javorina [Fig. 33] (Knutelski 1998).
PWT [Fig. 5] [Fig. 13]: Val. Spadowiec [Fig. 33] [Fig. 39], Val. nad
Capkami [Fig. 33], Kończysta Turnia [Fig. 14] [Fig. 33] [Knutelski
1988, 1993].
It was also quoted from the Tatra Mountains by
Knutelski & Skalski [1993], Petryszak [1993], Dieckmann & Behne [1994]
and Burakowski et al. [1995] but without localities.
In the Tatra Mountains O. croaticus was
discovered not long ago [Knutelski 1988] but only on northern slopes of the
Western Tatra region belonging to the Polish territory and on north-eastern
slopes of Slovakian Belianske Tatra, where it occurs mainly in deciduous beech
forest (Dentario glandulosae-Fagetum association) [Fig. 17] [Fig. 37] [Fig. 38] [Fig. 39], as well as in the alder and willow
brushwood (Alnetum incanae association), and reaches to 1050 m a.s.l.
Adults were sieved from the litter under different kind of trees: beech (Fagus
sylvatica), alder (Alnus incana (L.) MNCH.) and willow (Salix
caprea) in May and June, and once (August 17th) 1 ex. was scooped from the
floor plants using the sweep net.
O. croaticus, an European zoogeographical element, is a very rare
species, in Poland only known from the Western Carpathians (Male Pieniny Mts.,
Magura Spiska Mts., Tatra Mts.) [Knutelski
1988, 1991, 1993] [Knutelski & Skalski 1993] [Petryszak 1993]. In Europe
also noted from: Slovakia (Beskid Niski Mts.), Czech Republic (Bohemia),
Germany (Bayerische Alpen), Austria (Karawanken, Österreichische Alpen,
Salzburg and Tirol), Slovenia (Julische Alpen), Bosnia and Hercegovina (Bosnia:
Rudava), Croatia (without localities) and Italy (Venezia-Giulia) [Solari 1907]
[Porta 1932] [Junk 1936] [Horion 1951] [Kippenberg 1983] [Knutelski 1988]
[Strejček 1993] [Stüben 1999].
Onyxacalles
pyrenaeus (Boheman, 1844) [Fig. 29]
Acalles pyrenaeus BOH.: Smreczyński [1932], Endrödi
[1961], Jakuczun & Kuśka [1979],
Petryszak [1982], Knutelski & Szwałko [1992], Knutelski [1993],
Knutelski & Skalski [1993], Knutelski et al. [1986], Knutelski & Knutelska [1998].
BT [Fig. 8]: Černa val. [Fig. 34], Zdiar-Strednica [Fig. 34] [Knutelski & Knutelska 1998].
*SHT [Fig. 7]: Stary Smokovec [Fig. 34], 1070 m a.s.l., 1997/9/4, 1 ex. in a forest clearing of the lower montane belt was scooped using the sweep net; Try Studnicky [Fig. 34], 1126 m
a.s.l., 1993/9/15, 1 ex. in destroyed spruce forest by “halny” wind from the
litter, leg., det. and coll. SK.
*SWT: Borova voda [Fig. 34], 830 m a.s.l., 1993/9/14, 4 exx. In the brushwood
near the stream; Kycera [Fig. 34], 830-891 m a.s.l., 1993/9/14, 2 exx. In
xerothermophilous brushwood, leg., det. and coll. SK.
It is the first record of this
species for the High and Western Tatra region belonging to the Slovakian
territory.
PHT [Fig. 6] [Fig. 18]: Val. Filipka [Fig. 35],
1250-1280 m a.s.l., 1988/8/1, 1 ex. in the spruce forest of the upper montane
belt was scooped from the floor plants using the sweep net; Łysa
Skałka [Fig. 35], 950-1080 m a.s.l., 1988/6/30, 1 ex. in
the beech forest (Dentario glandulosae-Fagetum association), also
scooped from the floor plants; Wierch Poroniec - Rusinowa Clearing [Fig. 35], 980-1200 m a.s.l., 1991/6/11, 1 ex. in a spruce forest of the lower mountain belt
was taken directly from decayed branches of spruce, leg., det. and coll. SK.
It was just quoted from the Polish High Tatra region
but without localities [Knutelski & Szwałko 1992].
PWT [Fig. 5] [Fig. 13]: Brzeziny [Fig. 35], 1000 m
a.s.l., 1987/5/29, 1 ex. in willow-mountain-ash brushwood was sieved from the
litter with decayed branches under large-leaf willows (Salix caprea) and
mountain ash (Sorbus aucuparia L.); Val. Chochołowska [Fig. 35], 950 m a.s.l., 1985/7/8, 1 ex. in brushwood near
stream from the litter under willows, roses (Rosa canina L.) and
spruces; Val. Kościeliska [Fig. 35], 940 m a.s.l, 1986/7/5, 1 ex. in a spruce
forest of the lower montane belt from the litter, and at 960 m a.s.l.,
1986/7/4, 2 exx. in brushwood near the stream from the litter under spruce,
willow and alder; Val. Miętusia [Fig. 35], 1200 m a.s.l., 1985/10/8, 1 ex. in
spruce forest of the lower montane belt from the litter at forest side; Grzybowiec
[Fig. 35], 1410-1420 m a.s.l., 1996/7/24, 1 ex. and Wielka
Clearing [Fig. 35], 1250 m a.s.l., 1988/7/7, 1 ex., both individuals in
destroyed spruce forest by “halny” wind from the litter; Kazalnica [Fig. 35] [Fig. 14] [Fig. 17], 920-955 m a.s.l., 1986/7/28, 1 ex. and
9/5, 1 ex.; Kończysta Turnia [Fig. 35], 950-980 m a.s.l., 1987/7/16, 1 ex., all
specimens in beech forest (Dentario-glandulosae Fagetum association)
from the litter; Niżni Toporowy Pond - Wyżni Toporowy Pond [Fig. 35], 1100-1170 m a.s.l., 1990/7/9, 1 ex., in spruce
forests of the lower montane belt was scooped from the floor-plants using the
sweep net.
O. pyrenaeus in the Polish part of the Western Tatra region was
recorded before from other localities: Siwiańskie Turnie [Fig. 35], Hotarz [Fig. 35], Kazalnica [Fig. 35]
[Jakuczun and Kuśka 1979], Sarnia Skała [Fig. 35]
[Knutelski & Szwałko 1992], Val. Spadowiec [Fig. 35] [Knutelski 1993] and Val. Chochołowska [Fig. 35] [Burakowski
et al. 1995].
It was also quoted generally (without
localities) from the Tatra Mountains. [Smreczyński
1932] [Endrödi 1961] [Petryszak 1982] [Knutelski et al. 1986] [Knutelski &
Skalski 1993].
In the Tatra Mountains O. pyrenaeus mainly occurs in coniferous and mixed
coniferous-deciduous, and coniferous-coniferous forests as well as in destroyed
spruce forests by “halny” wind and brushwood near roads and streams (f. ex. in:
Dentario glandulosae-Fagetum, Piceo-Abietetum albae, Piceetum excelsae
subnormale, Piceetum tatricum abietetosum, Pinetum subalpinum calcicolum,
Epilobietea angustifolii associations) [Fig. 17] [Fig. 18] [Fig. 19] [Fig. 20] [Fig. 21] [Fig. 22] [Fig. 23]. Among the species from Cryptorhynchinae subfamily O.
pyrenaeus shows the highest limit of vertical distribution in the Tatra
Mountains, where 1420 m a.s.l. are reached [Fig. 13]. But
much more specimens were collected at a level of 1020 m of altitude [Fig. 36].
Larvae were reared in a decaying
branch of Sorbus chamaemespilus (L.) CR. and in a dead offshoot of S.
glabrata Hedl., representing Rosaceae plant family [Knutelski &
Szwałko 1992]. Probably they also live in the dead parts of other tree
species.
Adults were collected from dead
branches of mountain ash and spruces, tree trunks, pieces of bark, moss, under
sticks and stones as well as in the litter under dead branches of various trees
(spruce, fir, beech, alder, hazel), rock cracks and basalt crevices. They
usually hide during the day but sometimes, from June to September, especially
after heavy rainfalls they climb small firs and spruces as well as other
forest floor plants [Fig. 34] [Fig. 35] [Fig. 36] [Fig. 40] [Fig. 41].
O. pyrenaeus lives in the
mountains of south (Bosnien, north Italy), south-western (Pyrenees Mts.),
western and central parts of Europe [Burakowski et al. 1995] [Stüben 1999].
Discussion
The Tatra Mountains are inhabited by
5 weevil species of the Cryptorhynchinae subfamily: Cryptorhynchus lapathi,
Acalles camelus, A. commutatus, Onyxacalles croaticus and O. pyrenaeus. These
are about 36 % of all Cryptorhynchinae weevil species quoted from the whole
area of Poland and 50 % of the species living in Polish Carpathians [Burakowski
at al. 1995]. In the neighbouring Magura Spiska Mts., with the exception of A.
commutatus, there are the same species [Knutelski 2000] as recorded here
from the Tatra Mountains, but just a little bit further on, in the Pieniny
Spiskie Mts. [Knutelski & Witkowski 1995], only occur: C. lapathi, A.
camelus, O. pyrenaeus and Ruteria hypocrita Boh., 1837. Comparing
with Cryptorhynchinae of the Pyrenées Orientales and Hautes Pyrenées Mts.
[Stüben et al. 2000], where 13 weevil species of Cryptorhynchinae were
discovered, the fauna of this subfamily in the Tatra Mountains is strongly
poorer, but in the Pyrenees, C. lapathi and O. croaticus are not
found [Tempčre 1987].
Among the recorded species, O.
pyrenaeus is the most popular weevil of Cryptorhynchinae living in the
Tatra Mountains, and it was collected in all geobotanical Tatra regions, as
well as on Slovakian and Polish side of the Tatra Mountains. Other species are
rarer and occur in the narrower area of this mountain massif; only in Polish
parts of the Tatras, I found C. lapathi, and only in Slovakian
territory - A. camelus and A. commutatus, and only in Polish
Western Tatra and Slovakian Belianske Tatra O. croaticus was collected.
Acknowledgements
I am grateful to: Tatra National
Park and Tatranský narodný park for permissions to provide researches in the
Nature Reserve “Tatra”; Institute of Zoology of Jagiellonian University in
Kraków for granting my researches; Museum and Institute of Zoology of Polish
Academy of Science in Warszawa, Institute of Systematic and Animal Evolution of
Polish Academy of Science in Kraków and Slovak National Museum in Bratislava
for reaching me weevil collections; R. Laskowski PhD. head of Department of
Ecotoxycology, Jagiellonian University for help in photos scanning; and my wife
E. Knutelska, Msc. for drawing the map and help in collecting of weevils in the
Tatra Mountains.
References
Browicz, K. &
K. Zarzycki (1987):
XIV
International Botanical Congress. Excursion no. 23. National parks and nature
reserves in southern Poland. Berlin, 44
pp.
Burakowski, B.,
Mroczkowski, M. & J. Stefańska (1995):
Chrząszcze - Coleoptera. Ryjkowce
- Curculionidae, cz. 2. Katalog Fauny Polski, cz. XXIII, tom 20. - Dz.
Wyd. Muz. Inst. Zool. PAN., Warszawa.
Dieckmann, L. (1982):
Acalles-Studien. Ent. Nachr. u. Ber. 26, 195-209.
Dieckmann, L. & L. Behne (1994):
Ergänzungen und Berichtungen zu Band 10 und 11: 93. Familie:
Curculionidae. In: Lohse, G.A. & W.H. Lucht (Eds): Die Käfer Mitteleuropas.
3. Supplementband mit Katalogteil. Goecke & Evers Verlag, Krefeld.
Endrödi, S. (1961):
Az ormányosbogarak (Curculionidae) kárpátmedencei
lelőhelyadatai, III. Fol. ent. hung., 14, 279-316.
Horion, A. (1951):
Verzeichnis der Käfer Mitteleuropas (Deutschland, Österreich,
Tschechoslovakei) mit kurzen faunistischen
Angaben. 10. Stuttgart.
Jakuczun, L. & A. Kuśka (1979):
Ryjkowce (Coleoptera, Curculionidae)
zebrane w Dolinie Chochołowskiej w Tatrzańskim Parku Narodowym. Pol. Pismo Ent., 49, 371-384.
Junk, W. (1936):
Coleopterorum Catalogus, A. Hustache,
Curculionidae: Cryptorhynchinae, 151. s’Gravenshage.
Kippenberg, H. (1983):
25. Unterfamilie Cryptorhynchinae. In: Freude, H., Harde,
K.W. & G.A. Lohse (Eds): Die Käfer Mitteleuropas. Bd. 11, 342 S.
Goecke & Evers Verlag, Krefeld.
Knutelski, S.
(1988):
Acalles croaticus, Brisout, nowy dla fauny Polski (Coleoptera,
Curculionoidea). Pol. Pismo Ent., 58, 497-499.
____ (1991):
Nowe stanowiska kilku rzadko
spotykanych w Polsce ryjkowcowatych (Coleoptera, Curculionidae). Wiad
Entomol., 10,2, 85-88.
____ (1993):
Ryjkowce (Coleoptera: Curculionidae)
Tatr Polskich: I. Zgrupowania ryjkowców charakterystycznych środowisk Tatr
Zachodnich. Zesz. Nauk. UJ, Pr. Zool., 38,
73-179.
____ (2000):
Uwagi o ryjkowcach (Coleoptera:
Curculionoidea) Kotliny Nowotarskiej. Chrońmy
Przyr. Ojcz., 56, 2, 51-67.
Knutelski, S.,
Grzęda, E. & M. Mazur (1986):
Nowe stanowiska kilkunastu rzadko
spotykanych w Polsce ryjkowców (Coleoptera, Curculionidae). Zesz. Nauk. UJ,
Prace Zool., 31, 57-168.
Knutelski, S.
& P. Szwałko (1992):
Description of
the larva of Acalles pyrenaeus Boheman, 1844, with notes on ecology and
distribution of the species (Insecta, Coleoptera, Curculionidae:
Cryptorhynchinae). Faunist. Abhandl.,
18, 15, 191-196.
Knutelski, S.
& T. , Skalski (1993):
Fauna ryjkowców (Coleoptera:
Curculionoidea) polskiej części Magury Spiskiej. Zesz. Nauk. UJ,
Pr. Zool., 38, 181-208.
Knutelski, S.
& Z. Witkowski (1995):
Ryjkowce (Coleoptera: Curculionoidea)
obszaru przyszłych zbiorników wodnych Czorsztyn-Niedzica i Sromowce
Wyżne oraz przyległych pasm karpackich. Pieniny-Przyr. i Czł., 4,
59-76.
Knutelski, S.
& E. Knutelska (1998):
New records of
weevils for the Slovakian Belianske Tatra Mountains (Coleoptera: Apionidae;
Curculionidae), pp: 145-158. In:
Colonelli, E., Louw, S. & G. Osella (Eds):
Taxonomy, ecology and distribution
of Curculionoidea (Coleoptera: Polyphaga). Atti. Mus. Reg. Sci. nat. Torino.
Mirek, Z. & H.
Piękoś-Mirkowa (1992):
Flora and
vegetation of the Polish Tatra Mountains. Mount. Res. and Developm., 12,
2, 147-173.
Łomnicki,
(A.) M. (1866):
Przyczynek do fauny chrząszczów
galicyjskich, Kraków, 1-9.
____ (1868):
Wykaz chrząszczów
tatrzańskich według rozsiedlenia pionowego. Spraw. Kom. Fizyogr., 2,
1-152.
Nowicki, M. (1873):
Beiträge zur Insektenfauna Galiziens: Verzeichniss
galicischer Käfer. Jag. Univers.- Buchdruckerei. Krakau, pp. 7-52.
Petryszak, B.
(1982):
Ryjkowce (Coleoptera, Curculionidae)
Beskidu Sądeckiego. Rozpr. Hab. UJ, 68, 1-204.
____ (1993):
Ryjkowce (Coleoptera, Curculionidae)
Małych Pienin. Zesz. Nauk. UJ,
Pr. Zool., 38, 7-27.
Porta, A. (1932):
Coleopterorum Italica, Vol. V,
Rhynchophora-Lamellicornia. Stabilimento Tipografico Piacentino, Piacenza.
Smreczyński,
S. (1932):
Zbiór ryjkowców ś.p. Wojciecha
Mączyńskiego. Spraw. Kom.
Fizjogr., 65, 1-24.
Solari, A. &
F. (1907):
Studi sugli Acalles. Ann. Mus. Civ. Stor. Nat. Genova 3, 3,
478-551.
Strejček, J.
(1993):
Curculionidae, pp. 135-152. In: Jelinek, J. (Ed.). Check-list of Czechoslovak Insects IV (Coleoptera).
Suppl. 1. Folia Heyrovskyana, Praha.
Stüben, P.E.
(1999):
Die
westpaläarktischen Arten der Gattung Onyxacalles n. gen. (Coleoptera,
Curculionidae, Cryptorhynchinae). Ent. Bl. 95, 175-203.
Stüben, P.E., Bahr, F. & C. Bayer (2000):
Cryptorhynchinae-Exkursion in die Ost- und Zentralpyrenäen
(Coleoptera: Cryptorhynchinae). Weevil
News: <http://www.curci.de/>, No.1: 10 pp.
Szafer, W. (1962):
Tatrzański Park Narodowy. Praca
zbiorowa. Zakład Ochrony Przyrody PAN. Kraków, 675 pp.
Tempčre, G.
(1978) :
Coléoptčres Curculionidae de France, 6.
partie. Emtomops, Nice, 46: 213-232.
Adress of
author
Dr.
Stanisław Knutelski
Department of
Entomology and Mountain Station
Jagiellonian
University
PL-30-060
Kraków
R. Ingardena 6
Poland
Investigations were granted by
DS/IZ/ZS and BW/IZ/9 of Jagiellonian University grants from KBN.