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Abstract
raisa sukHoDoLskaYa Background and purpose: Despite plenty of data, papers on latitudinal aNaToLiY saVeLieV intraspecific body size variation in insects are scarce and in Ground Beetles Laboratory of Biomonitoring are absent at all. The aim of this research was to: (i) model the effect of the Institute of Ecology and Mineral Resource latitude into the body size variations in widespread carabid species; (ii) Management describe elytra length variation and body shape variation in latitude gradi- Academy of Sciences of Tatarstan Republic ul. Daurskaya 28, Kazan, 420087 Russia ent in studied species of Ground Beetles. e-mail: [email protected] Material and methods: Six carabid species from different provinces of Kazan (Volga Region) Federal University Russia (situated on different latitudes) were analyzed for six morphometric ul. Kremlevskaya 18, Kazan, 420008 Russia traits. We used linear models to quantify contribution of provinces latitude e-mail: [email protected] to traits variation. We applied relative warp analysis (a principal component Correspondence: analysis of the weight matrix) when analyzing effect of latitude on body Raisa Sukhodolskaya shape deviation in studied carabid species. e-mail: [email protected] Results: Different traits of certain species varied in differing ways under the influence of the same environmental factor. In three Carabus species and Key words: carabids, environmental factors, Pterostichus niger elytra length decreased towards the high latitudes, voice-counting method, converse Bergmann’s clines, Pterostichus melanarius demonstrated saw-tooth elytra length variation in saw-tooth variation, counter-gradient variation, latitude gradient and Poecilus cupreus – the counter-gradient one. linear models. Conclusion: Closely related species of carabids could act very differently, each individual species following or countering Bergmann’s rule in its own way. Explanation that takes into account the natural history, climatic cor- relations and sexual size dimorphism is needed to assess the observed contrast- ing geographic patterns and differences between species, morphometric traits and sexes, since size clines (e.g. Bergmann’s clines) may obey to multiple selec- tion pressures. Int Roduct Ion ody size and body parts proportions tend to follow some ecogeo - Bgraphical patterns, such as Bergmann’s or Allen’s rules. o Th se em - pirical postulates were originally formulated for endotherms, but sub - sequent work showed that ectotherms, either vertebrate or invertebrate, may show geographic body size patterns that sometimes do agree with the rules’ predictions (1, 2, 3). e Th literature on ecogeographical rules, both in endotherms and ectotherms, is abundant and the subject has received considerable attention in recent years (4, 5, 6). In the case of ectotherms either invertebrate or vertebrate, several hypotheses concern - ing body size variation have also been proposed, ree fl cting the evidence Received January 14, 2016. that some groups follow Bergmann’s and Allen’s rules, some show con - Revised August 28, 2016. verse or compound patterns, and some do not show any pattern at all. Accepted August 30, 2016. Converse Bergmann’s clines are much more frequent in ectotherms than R. Sukhodolskaya and A. Saveliev Latitudinal variation of body size in Ground Beetles Table 1. Sampling localities and sample size Region Latitude, °N Longitude, °E Number of sites Type of habitats Sample size 1 Stavropol region 45°02’ 41°55’ 6 Meadow, birch 76 2 Kemerovo region 54°56’ 87°14’ 20 Meadows, birch, lawn 1954 3 Novosibirsk region 55°27’ 79°33’ 14 Meadows, farmlands 360 4 Tatarstan Republic 55°47’ 49°06’ 53 Meadow, birch, oak, elm 11312 5 Maiy El Republic 56°42’ 47 52’ 14 Meadow, birch, oak 67 6 Udmurtia Republic 57°17’ 52°45’ 16 Birch, oak, elm 396 7 Cis_Ural 57° 01’ 57°9’ 21 Birch, oak, elm 58 8 Sverdlovsk region 58°42’ 61°20’ 6 Meadow 458 in endotherms, especially in insects (2, 3, 7). Body size in insects probably obeys to different ecophysiological fac - tors and evolutionary pressures than those in endotherms. Several authors have proposed, that size clines result from climatic selection on the duration of egg and nymphal development which indirectly affects body size and can produce different geographic patterns according to the nature of the life cycle (8, 9, 10). When revealing the mechanisms of clinal variation arising, several factors must be taken into account. A sys - temic review of the known literature on inter- and intra - specic fi variation in insect size along latitudinal or altitu - dinal clines was done to see how often such clines appeared and if they ree fl cted class-wide, species-specic fi , or ex - perimentally biased tendencies (11). Nearly even numbers of studies showed Bergmann clines and converse Berg - mann’s clines, where insects get smaller as latitude/altitude Figure 1. Illustration of measurements: 1-2 (elytra length), 3-4 (ely- increases. In fact, the majority of studies suggested no tra width), 5-6 (pronotum length), 7-8 (pronotum width), 9-10 clines at all. Small ranges may have obscured certain (head length), 11–12 (distance between the eyes). clines, while giant ranges may have introduced artifacts. Researchers examining interspecic fi patterns found clines less frequently than those examining intraspecic fi patterns MAte RIAL And Met Hods due to variation among species within the clades, which Collection sites and insect sampling. e Th material from 8 renders interspecic fi studies unhelpful. Bergmann’s rule large provinces have been analysed (Table 1). Wild speci- does not apply to hexapods with nearly the same consis - mens of carabids were sampled in die ff rent provinces of tency as it does to endothermic vertebrates. e Th validity Tatarstan Republic (53 sites) from 1996 till 2012. For the of Bergmann’s rule for any group and range of insects is sake of this research, specimens from other 7 provinces of highly idiosyncratic and partially depends on the study Russia were kindly presented to us from our colleagues design (11). M. Shelomi concluded that studies of „Berg - from Perm, Kemerovo, Stavropol, Udmurtia, Mariy El mann’s Rule“ should focus within species and look at Universities, Institute of Systematic and Zoology UD widespread but contiguous populations to account for all R AN and Visim Reserve and we measured those beetles sources of variation while minimizing error. ourselves (Table 1). Sample size of studied species varied u Th s in our study we tried to design investigations in from one site in each province to another, but was not less the way to obtain data that will allow us to reveal intra- than 100 specimens per species. In Tatarstan we tried to specic fi body size variation in carabid populations sam - sample beetles in their usual habitats, that were mainly pled in different areas of large provinces of Russia (cities similar between studied regions for all studied species as and their suburbs, natural cenosis with different vegeta - well as our collegues from other provinces. Beetles in every tion). We studied elytra length variation in latitudinal province were pitfall trapped in natural biotopes, cities, gradient in six carabid species, taking into account all suburbs and arable lands. Details on sample sizes are published and newly analyzed results. given in table S1 as supporting material. 274 Period biol, Vol 118, No 3, 2016. Latitudinal variation of body size in Ground Beetles R. Sukhodolskaya and A. Saveliev Figure 2. Effect of environmental factors into elytra variation in P. niger: a – elytra length, b – elytra width. Study organisms. We analyzed six carabid species: Carabus (Carabus) granulatus Linnaeus 1758, Carabus (Tachypus) cancellatus Illiger 1798, Carabus (Oreocarabus) hortensis Linnaeus 1758, Pterostichus melanarius Illiger 1798, Pterostichus niger Schaller 1783, Poecilus cupreus Linnaeus 1758. All of them are widespread in Paleartic, generalists, zoophagous and mesophilous. Morphometric analysis. All measurements were made with a Leitz RS stereoscopic dissecting microscope at a magnic fi ation of 10 diameters, using a calibrated ocular grid with a scale interval of 0.1 mm. For each specimen six variables were measured, including: elytra length and width, pronotum length and width, head length and dis - tance between eyes (Fig. 1). Mentioned points were used as landmarks in Procrustes analysis. Statistical analysis. All statistical analyses of the mor - phometric data were performed using R system (12). In this paper we present profound analysis of the one species – P. niger. At first we formed data set, coding each speci - men for the province and region, where it was sampled and for other environmental factors. e Th list of variables and codes used in each column are presented as support - ing material in Tables S2 and S3. e Th n we used linear models to reveal, which factor (province, anthropogenic or habitat type) affected signic fi antly to traits variation. Figure 3. Effect of latitude into the elytra length variation in differ - For example, the model which estimated the variation of ent species of carabids; the vertical dotted line denotes the normal- elytra length was recorded as follows (using the R syntax): ized basic means of elytra length in concrete species in the centre of its area; each region has its own color, colors change in rainbow **** Elytra.Length~fSex/(f Region+fAnthropogen+f Habi turn – from the bottom (low latitudes, red color) to the top (high tat), where fSex – the factor, representing sex, f Region- latitudes, violet color): – females, – males. factor, representing the area, etc. Variance analysis (ANO- VA) of models was used for effects signic fi ance test. We estimated the ee ff cts for all variables and their interactions base of comparison (the 95% cond fi ence level and a nor - for every trait and confidence intervals (using Student mal approximation was used). Besides the confidence criteria) and residual statistics (errors). Results were pre- intervals for the main ee ff cts of sex, some other variables sented as estimated effects and their cond fi ence intervals were also displayed. Modeling results in P. niger are shown were used to present modeling results in figures and ta - as supporting information in table S4. Table S5 shows the bles; interaction eec ff ts were compared with that of the impact of studied factors to elytra length variation. Period biol, Vol 118, No 3, 2016. 275 R. Sukhodolskaya and A. Saveliev Latitudinal variation of body size in Ground Beetles e Th other v fi e species had been treated in the same way For the purposes of shape analysis 12 landmarks were and results had been published earlier (13, 14, 15, 16, 17). recorded on the beetles body (Fig. 1). e Th se landmarks In this paper we discuss results only how latitude contrib- were chosen for their ability to capture the overall shape uted to the elytra length variation of the beetles’ body. e Th specimens were scaled to unit * – data was taken from M.L.Minetz, V. V. Grichik (18) * – data was taken from I. N. Isaeva (19) * – data was taken from V. V. Brygadyrenko, O. V., Ko - rolev (20), ** – the same – from Y. N. Belova (21), *** – the same – from S. L. Kallio (22) Figure 4. Elytra length variation in latitudinal gradient (from left to right in the images = from low latitudes towards high latitudes; --- – linear trends). 276 Period biol, Vol 118, No 3, 2016. Latitudinal variation of body size in Ground Beetles R. Sukhodolskaya and A. Saveliev C. granulatus C. cancellatus C. hortensis P. niger P. melanarius Poec. cupreis Figure 5. Results of the relative warp analysis (a principal component analysis of the weight matrix) when analyzing effect of latitude on body shape shifts in studied species of carabids. Period biol, Vol 118, No 3, 2016. 277 R. Sukhodolskaya and A. Saveliev Latitudinal variation of body size in Ground Beetles centroid size and their landmarks configurations were latitudes. In Poec. cupreus means of elytra length did not aligned according to the best overall t, fi using the Gener - show signic fi ant deviations in latitude gradient (Fig. 4). alized Procrustes Analysis (GPA) and shape variables were Such differences echoed shape variation as well. Re - obtained as the partial warp scores and uniform compo - sults of relative warp analysis (a principal component nent. Centroid size was also calculated and retained for analysis of the weight matrix) showed that in studied spe- each specimen. To describe size changes in shape under cies centroids of southern regions stood lower relatively to different environmental factors we performed a relative the 2-nd axis, than the centroids of more northern re - warp analysis (a principal component analysis of the gions, the second axis reflected then systematic body weight matrix) and examined the pattern of shape varia - shape variation in latitude gradient. On the contrary, in tion under different environmental effects. Thin-plate P. melanarius distribution of coding regions cenroids in spline deformation grids for certain factor ee ff ct were gen - the factor plane was irregular (Fig. 5). erated to facilitate description of shape variation in differ - ing environmental conditions. Additionally, shape varia - d Iscuss Ion tion under differing environmenta l factors was represented by the matrix of Procrustes distances. e Th earlier studies showed that relatively large insects with long development times tended to express converse Bergmann clines, whereas relatively small insects with short Resu Lts development times trended to express Bergmann’s clines In order to illustrate the way of our analysis we dem - (2). When the available time for growth decreases, the in - onstrate the results of linear models when estimating the sect will be selected to mature earlier at the cost of a reduced role of main environmental factors in body size variation adult size that could also reduce fecundity. This scenario in one of the studied species – P. niger (Fig. 2). e Th other results in a detectable pattern in development time and size species were treated in the same way. along an environmental gradient; with a monotonic in - Factor of latitude position affected different traits in crease with season length (23). In univoltine insects, which different ways: elytra length decreased in the regions can only overwinter at a particular developmental stage, northwards of Tatarstan (see Table 1) (Intercept in our their developmental time is restricted by habitat tempera - model). On the contrary, elytra width was broader in ture. e Th decrease in body size in cooler habitats can be those regions. e Th other traits did not vary signic fi antly. explained by selection for a shorter developmental time, As for other environmental factors (anthropogenic state, which results in smaller body size. e Th refore, the converse vegetation), they did take part in the P. niger traits varia- of Bergmann’s rule is considered to be a result of climatic tion in size, e. g. in shadowed biotopes (elm, lime) elytra adaptation in univoltine arthropods (8, 10). This is the so- length decreased but elytra width increased. called „converse Bergmann’s rule“ (24,) that has been well documented (25, 26, 27, 28). In our study we registered e Th n we compiled data concerning the only elytra body size decrease in Carabus species and P. niger. e Th y length variation in latitudinal gradient, taking results in P. conr fi med the previous studies in C. granulatus, when body niger, mentioned above, and the results in v fi e carabid spe - size in that species decreased from Middle Taiga towards cies, that had been published (See „Materials and meth - Forest Tundra (29). It is noteworthy that in Carabus species ods”) (Fig. 3): deviations in elytra length in latitude gradi- nor bivoltine, nor biennial cycles are implemented (30). ent were not similar in all six species. For example, e Th se facts explained continuous decrease of body size in southwards from Tatarstan (it is the centre of the areas), in our studied species of Carabus genus in latitude gradient. Kemerovo region, elytra length in C. granulatus decreased, In other words elytra length variation in those species fol- in P. niger alters only males and in Poec. cupreus no devia- lowed converse Bergmann rule. tions were observed. Another example: northwards from Tatarstan, in Udmurtia, elytra length in C granulatus be- The second opinion on the body size clines is that came longer only in females, in C. cancellatus, C. hortensis variation in number of generations per season (i.e. volt - and P. melanarius elytra length decreasd in both sexes, but inism) ae ff cts time constraints. e Th traditional view about in P. niger that trait did not change at all. how latitudinal or altitudinal gradient in season length Because of the cognitive value of the elytra length (the ae ff cts the evolution of development time and body size in potentially multivoltine insects was developed by S. majority of carabidologists equate this trait to the body size) Masaki (8, 9) and formalized by D. Ro ff (10, 23) and Y. we tracked elytra length value variation in latitudinal gradi- ent in studied carabid species. Results demonstrated three Iwasa (31). e Th y assumed that development time and body types of that variation: in C. granulatus, as well as in C. size are positively correlated among genotypes, and in - cancellatus, C. hortensis elytra length decreased towards the sects, use all available time for growth to maximize adult body size and thus fecundity. Consequently, both devel- high latitudes. e Th same tendency in a lesser degree dem - onstrated P. niger. P. melanarius showed „saw-tooth” vari- opment time and body size are expected to increase along ation of elytra length in latitudinal gradient, when trait a gradient of increasing season length (i.e. with decreasing value periodically increased and decreased towards the high latitude or altitude) as long as voltinism does not change, 278 Period biol, Vol 118, No 3, 2016. Latitudinal variation of body size in Ground Beetles R. Sukhodolskaya and A. Saveliev giving rise to a converse Bergmann cline. However, sharp able after the confound investigations of carabids intra – decreases in both traits are expected at the season lengths specic fi shape variation, including common garden ex - that facilitate the emergence of a new generation within periments as well. the season, because time available per generation decreas - es at these transitions. u Th s, the traditional saw-tooth conc Lus Ion cline arises across phenologies because of genetic adapta- Previous studies in body size clines in arthropods re- tion to local conditions. e Th examples of saw-tooth varia - sumed that taken as a whole these studies suggest no gen - tion were presented in recent years (32, 33). eral latitudinal relationship with respect to body size To our view that mechanism worked in our study in among all insect groups, although positive, negative or relation to P. melanarius. According to A. V. Matalin (34, null relationships may occur in specic fi taxa in any par - 35) this species has polyvariant life cycle. At middle lati - ticular biogeographical region. That occurred, to our tudes (primarily, in forest steppe and mixed coniferous mind, because of the irrespective designs of investigations, and broad-leaved forests) with the long growing season which must take into account that even very close species (not less than 5.5–6 months) and with a signic fi ant coe- and their certain traits may act differently in latitude gra - notic diversity (including meso- and microclimatic diver - dient. We showed three types of latitude body size varia- sity) the period of activity is prolonged, often covering hot tion in carabids. Our data confirmed that this parameter summer months. As a result, a partial or complete devel - can follow converse Bergmann rule, demonstrate saw- opment of the second generation is observed in this spe- tooth or counter gradient variation. Explanation that cies throughout the season. Since there are two genera- takes into account the natural history, climatic correla - tions, body size of the beetles is not large. Further to the tions and sexual size dimorphism is needed to assess the north the duration of the reproductive season decreases observed contrasting geographic patterns and differences and life-cycle in P. melanarius becomes univoltine, hence between species, morphometric traits and sexes, since size allowing more time for this single generation. e Th re is clines (e.g. Bergmann’s clines) may obey to multiple selec - enough time to the larva development and the body size tion pressures that are not only dependent on temperature of imago becomes larger. Similar processes were observed constraints but also on other climatic and biotic factors in other insects (32, 33, 36, 37, 38). Further to the north that could inu fl ence body size. because of the temperature constraints, breeding period becomes shorter and body size of the beetles again de - Acknowledgements: The authors thank Prof. N. Ere - creases. Onwards further to north P. melanarius has bien- meeva, Prof. V. Mordkovich, Prof. L. Esyunin, Prof. E. nial life cycle (39) and its body size, correspondingly, in- Chenikalova, Dr S. Dedyukhin, Dr V. Matveev, Dr N. creased again by reasons of prolonged time of development. Ukhova for beetles collections from different provences of Rus - In addition the third pattern of body size variation in sia for the purposes of morphometric analysis. latitude gradient can occur. It is counter-gradient varia- tion, known as the hypothesis of latitude compensation (40). e Th mechanism can be described as follows: in high Refe Rences latitudes specimen compensate short breeding period by 1. R AY C 1960. The application of Bergmann’s and Allen’s rules to higher (it is genetically coded) rate of growth, compared the poikilotherms. J. Morphology. 106: 85–108 with conspecic fi ians in low latitudes. In simplest case the http://dx.doi.org/10.1002/jmor.1051060104 2. BLANCKENHORN W U, DEMONT M 2004 Bergmann and rate of growth is the body size per the unit of development Converse Bergmann Latitudinal Clines in Arthropods: Two Ends time, the utterly exact compensation of breeding season of a Continuum? Integr. Comp. Biol., 44: 413–424 constraints at the certain latitude (the environmental 3. BIDAU C D, MARTI DA 2007 Dichroplus vittatus (Orthoptera: component) will occur in that situation, when growth rate Acrididae) follows the converse to Bergmann’s rule although male morphological variability increases with latitude. B Entomol Res. (genetic component) evolves in the way to keep pheno - 97: 69–79 typic body size equal at all latitudes. If increasing growth 4. BLACKBURN T M, GASTON K J, LODER N 1999 Geograph- rate perfectly compensates for the decrease in generation ic gradients in body size: a clarification of Bergmann’s rule. Divers. time, body size remains constant over the whole gradient Distrib. 5: 165–174 of season length. Possibly that pattern of latitudinal elytra 5. ASHTON K G 2002 Patterns of within-species body size variation size variation we observed in Poec. cupreus. Additionally, of birds: strong evidence for Bergmann’s rule. Global Ecol. Biogeogr. 11:505–523 http://dx.doi.org/10.1046/j.1466-822X.2002.00313.x the lack of the pronounced u fl ctuations in elytra length 6. VINARSKI M 2015 On the applicability of Bergmann rule to in Poec. cupreus might be determined by the lack of sam - arthropods. Zshurnal obshey biologii 74(5): 327-339 [in Russian] ples in northern regions: the highest latitude where that 7. BRENNAN J, FAIRBAIRN D 1995. Clinal variation in morphol - species was sampled in our study was 55°47’N. ogy among eastern populations of the waterstrider, Aquarius remi- gis Say (Hemiptera, Gerridae). Biol. J. Linn. Soc. 54: 151–171 As for latitude shape variation in studied species, we http://dx.doi.org/10.1111/j.1095-8312.1995.tb01029.x failed to find papers concerning this subject. Very scarce 8. MASAKI S 1967 Geographic variation and climatic adaptation in data in beetles shape variation dealt one – two species in a field cricket (Orthoptera:Gryllidae). Evolution. 21: 725–741 very local scale (41, 42). Discussion on this subject is prob- http://dx.doi.org/10.2307/2406770 Period biol, Vol 118, No 3, 2016. 279 R. Sukhodolskaya and A. Saveliev Latitudinal variation of body size in Ground Beetles 9. MASAKI S 1978 Climatic adaptation and photoperiodic response 29. FILIPPOV B 2008 The ways of adaptation and ecological mecha - in the bandlegged ground cricket. Evolution. 26: 587–600 nisms of Ground Beetles (Coleoptera, Carabidae) familiarization http://dx.doi.org/10.2307/2407055 in Russian plane north. Ph. D. thesis. Moscow. 367 p [in Russian] 10. ROFF D 1980 Optimizing development time in a seasonal environ - 30. MATALIN A V 2011 Life-cycles of Ground Beetles (COLEOP- ment: the ‘ups and downs’ of clinal variation. Oecologia. 45: 202– TER A, CAR ABIDAE) in Western Palearctic. Ph. D. Thesis, Mos - 208 http://dx.doi.org/10.1007/BF00346461 cow. 40 p [in Russian] 11. SHELOMI M 2012 Where Are We Now? Bergmann’s Rule Sensu 31. IWASA Y, EZOE H, YAMAUCHI A 1994 Evolutionary stable Lato in Insects. Amer. Nat. 180 (4): 511-519 seasonal timing of univoltine and bivoltine insects. In: Danks H http://dx.doi.org/10.1086/667595 V(ed) Insect Life-cycle Polymorphism. Kluwer Academic Publish - 12. R DEVELOPMENT CORE TEAM 2011 R: A language and en- ers, Netherlands, pp. 69–89 http://dx.doi.org/10.1007/978-94-017-1888-2_4 vironment for statistical computing. R Foundation for Statistical Computing, Vienna, Austria. http://www.r-project.org/. 32. NYGREN G H, BERGSTR?M A, NYLIN S. 2008. Latitudinal 13. SUKHODOLSK AYA R, SAVELIEV A 2014 Effects of Ecological body size clines in the butterfly Polyommatus icarus are shaped by Factors on Size_Related Traits in the Ground Beetle Carabus gran- gene-environment interactions. 14pp. Journal of Insect Science 8:47 ulatus L. (Coleoptera, Carabidae). Russian Journal of Ecology 45: http://dx.doi.org/10.1673/031.008.4701 414-420 http://dx.doi.org/10.1134/S1067413614050142 33. VALIMAKI P, KIVELA S M, MAENPA A M I, TAMMARU T 14. SUKHODOLSK AYA R 2014 Variation in Body Size and Body 2013 Latitudinal clines in alternative life histories in a geometrid Shape in Ground Beetle Pterostichus melanarius Ill. (Coleoptera, moth. Journal of Evolutionary Biology. 26: 118–129 Carabidae). Journal of Agri-Food and Applied Sciences 2(7 ):196-205 34. MATALIN A 2015 Specific Manifestations of Polyvariant Life 15. SUKHODOLSK AYA R, SAVELIEV A 2012 The inu fl ence of en - Cycles in Ground Beetles (Coleoptera and Carabidae) along a vironmental factors on morphometric variation and sexual dimor - Latitudinal Gradient. Biology Bulletin 42: 526–530 phism in Ground Beetles (the case with Carabus cancellatus Ill.). http://dx.doi.org/10.1134/S1062359015660036 Applied Entomology 3(2): 28-38 [in Russian] 35. MATALIN A 2006 Geographical variation of life-cycle in Pteros- 16. SUKHODOLSK AYA R 2013 Intraspecific body size variation in tichus melanarius (Coleoptera, Carabidae). Zoological Journal 85: Ground Beetles (Coleoptera, Carabidae) in urban-suburban-rural- 573-585 [in Russian] natural gradient. Acta Biologica Universitatis Daugavpiliensis. 13 (1): 36. HAWKINS B A, LAWTON J H 1995 Latitudinal gradients in 121 – 128. butterfly body sizes: is there a general pattern? Oecologia. 102: 31-36 17. SUKHODOLSK AYA R, SAVELIEV A, Muhammetnabiev T. http://dx.doi.org/10.1007/BF00333307 2016 Sexual Dimorphism of Insects and Conditions of Its Mani - 37. HAWKINS B A 1995 Latitudinal body-size gradients for the bees festation. Research Journal of Pharmaceutical, Biological and Chem- of the eastern United States. Ecological Entomology 20: 195-198 ical Sciences. 7(2): 1992 – 2001. http://dx.doi.org/10.1111/j.1365-2311.1995.tb00446.x 18. MINETZ M, GRICHIK V 2007 Phenotypic and morphological 38. HU Y, ZHU X, LEI C 2011 Development Time and Body Size in traits variation in the populations of Ground Beetle Carabus gran- Eupolyphaga sinensis Along a Latitudinal Gradient From China . ulatus l. (Coleoptera, Carabidae) on the territory of Bielorussia. Environmental Entomology. 40(1):1-7. Herald of BSU 2(2): 69 – 74 [in Russian] http://dx.doi.org/10.1603/EN09365 19. ISAEVA I 2009 Phenotypic variation in Carabus cancellatus (In- 39. WALLIN H. 1989 The influence of different age classes on the secta, Coleoptera, Carabidae) from the population of the Zhigu - seasonal activity and reproduction of four medium-sized carabid levskiy Reserve. Samarskaya Luka: the problems of regional and species inhabiting cereal fields . Ecography 12(3): 201 – 212 global ecology 18(2): 180-184 [in Russian] http://dx.doi.org/10.1111/j.1600-0587.1989.tb00839.x 20. BRIGADIRENKO V, KOROLEV O 2015 Morphological poly- 40. CONOVER D O, SCHULTZ E T 1995 Phenotypic similarity and morphism in an urban population of Pterostichus melanarius (Il- the evolutionary significance of counter gradient variation. Trends liger, 1798) (Coleoptera, Carabidae). Graellsia 71(1): e025 in Ecology and Evolution. 10: 248–252 http://dx.doi.org/10.3989/graellsia.2015.v71.126 http://dx.doi.org/10.1016/S0169-5347(00)89081-3 21. BELOVA Y 2012 Fauna and population structure of soil inverte- 41. ALIBERT P, MOUREAU B, DOMMERGUES J L, DAVID B brates in forest ecosystems of Vologda region (the case of Coleop - 2001 Differentiation at a microgeographical scale within two spe - tera, Carabidae) Ph. D. thesis. Petrozavodsk 190 p. [in Russian] cies of ground beetle, Carabus auronitens and C. nemoralis (Cole - 22. K ALLIO S 2014 Relationship between species traits and landscape optera, Carabidae): a geometrical morphometric approach. Zool Scr. extent in ground beetles (Coleoptera: Carabidae). Ph.D. thesis. Ot- 30:299–311 tawa. 121 p 42. BENITEZ H A 2013 Assessment of Patterns of Fluctuating Asym - 23. ROFF D A 1983 Phenological adaptation in a seasonal environ- metry and Sexual Dimorphism in Carabid Body Shape. Neotrop ment: A theoretical perspective. In: Brown V K, Hodek I (ed) Dia - Entomol. 42:164–169 DOI 10.1007/s13744-012-0107-z pause and life cycle strategies in insects. Dr W Junk Publishers. pp. http://dx.doi.org/10.1007/s13744-012-0107-z 253–270 24. MOUSSEAU T A 1997 Ectotherms follow the converse to Berg - mann’s Rule. Evolution 51: 630–632 su PPo Rt In G Info RMAt Ion http://dx.doi.org/10.2307/2411138 25. NYLIN S, SVARD L 1991 Latitudinal patterns in the size of Eu- Additional supporting information may be found in ropean butterflies. Holarctic Ecology 14: 192 – 202 the online version of this article. http://dx.doi.org/10.1111/j.1600-0587.1991.tb00652.x 26. BLANKENHORN W U, FAIRBAIRN D J 1995 Life-history S1 Sample size of carabid species, sampled in dif - adaptations along a latitudinal cline in water strider Aquarius remi - ferent provences gis (Heteroptera: Gerridae). Journal of Evolutionary Biology. 8: 21 S2 Data set for P. niger -41 http://dx.doi.org/10.1046/j.1420-9101.1995.8010021.x 27. TELFER M G, HASSAL M 1999 Ecotypic differentiation in the S3 Denotations for columns in S2 grasshopper Chorthippus brunneus: life history varies in relation to S4 Results of modeling of die ff rent factors ee ff ct on climate. Oecologia. 121: 245 – 254 traits variation in P. niger 28. JOHANSSON F 2003 Latitudinal shift in body size of Enallagma S5 Ee ff cts of environmental factors on elytra length cyathigerum (Odonata). Biogeography. 30: 29 – 34 http://dx.doi.org/10.1046/j.1365-2699.2003.00796.x variation in P. niger, results of linear modeling 280 Period biol, Vol 118, No 3, 2016. Electronic Supplements to: Sukhodolskaya and Saveliev, Periodicum Biologorum, 2016, 118(3):273‐280 DOI: 10.18054/pb.2016.118.3.3918 S1 Sample size of carabid species, sampled in different provences Sample size of carabid species, sampled in different regions Region/Species C. granulatus C. cancellatus C. hortensis P. melanarius P. niger Poec. cupreus total Stavropol 5 region 71 76 Kemerovo 104 83 region 84 271 Tatarstan 993 1664 1170 2394 690 1865 Republic Mariy El 24 38 9 Republic Udmurtia 71 114 97 110 14 Republic Cis_Ural 14 12 18 Sverdlovsk 138 120 region Novosibirsk region 360 360 total 1168 1792 1291 2697 934 2380 10350 Electronic Supplements to: Sukhodolskaya and Saveliev, Periodicum Biologorum, 2016, 118(3):273-280 DOI: 10.18054/pb.2016.118.3.3918 S2 Data set for P. niger 7 1 3 5 4 4 2 9.7 2.1 3.5 3.6 3 2.1 -999 -999 -999 -999 -999 -999 7 1 3 5 4 4 2 9.3 2.1 3.2 3.3 2.7 1.8 -999 -999 -999 -999 -999 -999 7 1 3 5 4 4 2 10 2.3 3.6 3.9 2.8 2 -999 -999 -999 -999 -999 -999 7 1 3 5 4 4 2 9.1 2 3.3 3.5 2.5 1.8 -999 -999 -999 -999 -999 -999 7 1 3 5 4 4 2 10.6 2.6 3.7 4.1 3.2 2.3 -999 -999 -999 -999 -999 -999 7 1 3 5 4 4 2 11.3 2.5 3.9 4.2 3.1 2.2 -999 -999 -999 -999 -999 -999 7 1 3 5 4 4 2 12 2.7 4.1 4.6 3.2 2.3 -999 -999 -999 -999 -999 -999 7 1 3 5 4 4 2 11.1 2.6 3.6 3.8 3.2 2.1 -999 -999 -999 -999 -999 -999 7 1 3 5 4 4 2 10.4 2.6 3.6 3.9 2.8 2.1 -999 -999 -999 -999 -999 -999 7 1 3 5 4 4 2 10.2 2.5 3.4 3.7 3.1 2 -999 -999 -999 -999 -999 -999 7 1 3 5 4 4 2 12 3.1 4 4.5 3 2.5 -999 -999 -999 -999 -999 -999 7 1 3 5 4 4 2 11.3 2.7 3.7 4.2 3.3 2.3 -999 -999 -999 -999 -999 -999 7 1 3 5 4 4 2 10.2 2.6 3.4 3.8 2.9 2.2 -999 -999 -999 -999 -999 -999 7 1 3 5 4 4 2 10.9 2.6 3.5 4 2.8 2.1 -999 -999 -999 -999 -999 -999 7 1 3 5 4 4 2 10.5 2.4 3.5 3.6 2.6 2 -999 -999 -999 -999 -999 -999 7 1 3 5 4 4 2 10.6 2.6 3.7 4 2.7 2.1 -999 -999 -999 -999 -999 -999 7 1 3 5 4 4 2 11.4 2.8 3.8 4.1 2.9 2.3 -999 -999 -999 -999 -999 -999 7 1 3 5 4 4 2 11.1 2.7 3.3 4 2.89 2.2 -999 -999 -999 -999 -999 -999 7 1 3 5 4 4 2 10.3 2.4 3.4 3.9 2.7 2.1 -999 -999 -999 -999 -999 -999 7 1 3 5 4 4 2 12.4 3 3.5 4.6 3.3 2.4 -999 -999 -999 -999 -999 -999 7 1 3 5 4 4 2 10.2 2.6 3.5 4.2 2.8 2.1 -999 -999 -999 -999 -999 -999 7 1 3 5 4 4 2 10.7 2.4 3.7 3.7 3 2.1 -999 -999 -999 -999 -999 -999 7 1 3 5 4 4 2 10.1 2.6 3.6 4 2.8 2.2 -999 -999 -999 -999 -999 -999 7 1 3 5 4 4 2 10 2.5 3.2 4.1 2.7 2.1 -999 -999 -999 -999 -999 -999 7 1 3 5 4 4 2 11.2 2.8 3.8 4.2 3 2.2 -999 -999 -999 -999 -999 -999 7 1 3 5 4 4 2 10.9 2.6 3.6 4 2.8 2.1 -999 -999 -999 -999 -999 -999 7 1 3 5 4 4 2 10.5 2.7 3.5 3.9 2.5 2.3 -999 -999 -999 -999 -999 -999 7 1 3 5 4 4 2 11.3 2.8 3.5 4.3 2.9 2.2 -999 -999 -999 -999 -999 -999 7 1 3 5 4 4 2 10.4 2.5 3.5 3.8 2.5 1.9 -999 -999 -999 -999 -999 -999 7 1 3 5 4 4 2 11.3 2.8 3.8 4 3 2.2 -999 -999 -999 -999 -999 -999 7 1 3 5 4 4 2 9.3 2.3 3.4 3.9 2.5 2 -999 -999 -999 -999 -999 -999 7 1 3 5 4 4 2 9.4 2.6 3.5 3.6 2.7 1.9 -999 -999 -999 -999 -999 -999 7 1 3 5 4 4 2 10.5 2.8 3.8 4 2.8 2.1 -999 -999 -999 -999 -999 -999 7 1 3 5 4 4 2 11.2 2.6 4 4.3 3 2.2 -999 -999 -999 -999 -999 -999 7 1 3 5 4 4 2 10.6 2.5 3.5 4.3 3 2.2 -999 -999 -999 -999 -999 -999 7 1 3 5 4 4 2 10.8 2.4 3.8 4.2 2.9 2.3 -999 -999 -999 -999 -999 -999 7 1 3 5 4 4 2 11.1 2.7 3.7 4.1 2.9 2.2 -999 -999 -999 -999 -999 -999 7 1 3 5 4 4 2 11 2.6 4 3.9 3.2 2.2 -999 -999 -999 -999 -999 -999 7 1 3 5 4 4 2 11 2.6 3.6 4.2 3 2.3 -999 -999 -999 -999 -999 -999 7 1 3 5 4 4 2 11.1 2.5 3.7 4.1 3 2.2 -999 -999 -999 -999 -999 -999 7 1 3 5 4 4 2 10.7 2.5 3.6 4 3 2.1 -999 -999 -999 -999 -999 -999 7 1 3 5 4 4 2 10.9 2.5 3.7 3.7 3.1 2.1 -999 -999 -999 -999 -999 -999 7 1 3 5 4 4 2 12 2.6 4 4.3 3.4 2.2 -999 -999 -999 -999 -999 -999 7 1 3 5 4 4 2 11.8 3.1 4 4.5 3.2 2.4 -999 -999 -999 -999 -999 -999 7 1 3 5 4 4 2 10.2 2.7 3.7 3.6 2.8 2.1 -999 -999 -999 -999 -999 -999 7 1 3 5 4 4 2 10.8 2.8 3.7 4 3.1 2 -999 -999 -999 -999 -999 -999 7 1 3 5 4 4 2 12.2 3.2 4.1 4.6 3 2.2 -999 -999 -999 -999 -999 -999 7 1 3 5 4 4 2 10.3 2.5 3.4 3.6 2.6 2 -999 -999 -999 -999 -999 -999 7 1 3 5 4 4 2 11.3 2.8 3.7 3.9 3 2.1 -999 -999 -999 -999 -999 -999 7 1 3 5 4 4 2 10.9 2.8 3.8 4.2 2.9 2.1 -999 -999 -999 -999 -999 -999 7 1 3 5 4 4 2 11.8 2.7 4 4.3 3 2.2 -999 -999 -999 -999 -999 -999 7 1 3 5 4 4 2 11 2.6 3.7 3.7 2.8 2.1 -999 -999 -999 -999 -999 -999 7 1 3 5 4 4 2 11 2.5 3.5 3.9 2.7 2.1 -999 -999 -999 -999 -999 -999 7 1 3 5 4 4 2 10.2 2.5 3.3 3.7 2.5 1.9 -999 -999 -999 -999 -999 -999 7 1 3 5 4 4 2 10.1 2.3 3.3 3.6 2.3 1.8 -999 -999 -999 -999 -999 -999 7 1 3 5 4 4 2 10.7 2.7 3.4 3.9 2.5 2.1 -999 -999 -999 -999 -999 -999 7 1 3 5 4 4 2 10.6 2.6 3.7 3.8 2.8 2.1 -999 -999 -999 -999 -999 -999 Electronic Supplements to: Sukhodolskaya and Saveliev, Periodicum Biologorum, 2016, 118(3):273-280 DOI: 10.18054/pb.2016.118.3.3918 7 1 3 5 4 4 2 12 3 3.9 4.3 2.9 2.4 -999 -999 -999 -999 -999 -999 7 1 3 5 4 4 2 10.7 2.6 3.7 3.8 2.8 2.1 -999 -999 -999 -999 -999 -999 7 1 3 5 4 4 2 11.8 2.8 3.8 4.2 2.9 2.2 -999 -999 -999 -999 -999 -999 7 1 3 5 4 4 2 10.4 2.4 3.2 3.7 2.8 2.1 -999 -999 -999 -999 -999 -999 7 1 3 5 4 4 2 10.7 2.5 3.5 3.8 2.9 2 -999 -999 -999 -999 -999 -999 7 1 3 5 4 4 2 11.7 2.6 3.5 3.8 3.1 2.1 -999 -999 -999 -999 -999 -999 7 1 3 5 4 4 2 10.8 2.7 4 4.2 3.4 2.2 -999 -999 -999 -999 -999 -999 7 1 3 5 4 4 2 13.4 3.4 4.2 5.2 4.2 2.8 -999 -999 -999 -999 -999 -999 7 1 3 5 4 4 2 11.8 2.8 4.1 4.5 3.5 2.4 -999 -999 -999 -999 -999 -999 7 1 3 5 4 4 2 10.7 2.8 3.8 4.3 3.3 2.2 -999 -999 -999 -999 -999 -999 7 1 3 5 4 4 2 11.9 3 4 4.4 3.6 2.6 -999 -999 -999 -999 -999 -999 7 1 3 5 4 4 2 10.4 2.4 3.6 3.9 3.2 2.2 -999 -999 -999 -999 -999 -999 7 1 3 5 4 4 2 10.6 2.6 3.7 3.8 3.4 2.2 -999 -999 -999 -999 -999 -999 7 1 3 5 4 4 2 11.6 2.6 4 4.3 3.5 2.2 -999 -999 -999 -999 -999 -999 7 1 3 5 4 4 2 11.1 2.8 3.9 4 3.3 2.3 -999 -999 -999 -999 -999 -999 7 1 3 5 4 4 2 9.9 2.5 3.7 3.8 2.8 1.9 -999 -999 -999 -999 -999 -999 7 1 3 5 4 4 2 10.8 2.8 3.6 4.2 2.9 2.2 -999 -999 -999 -999 -999 -999 7 1 3 5 4 4 2 10.2 2.6 3.4 4.2 2.8 2.1 -999 -999 -999 -999 -999 -999 7 1 3 5 4 4 2 11.8 2.5 3.9 3.7 3.4 2 -999 -999 -999 -999 -999 -999 7 1 3 5 4 4 2 10.5 3 3.7 4.3 3 2.2 -999 -999 -999 -999 -999 -999 7 1 3 5 4 4 2 12 3.1 4 4.6 3.1 2.4 -999 -999 -999 -999 -999 -999 7 1 3 5 4 4 2 12.4 2.9 3.8 4.6 3 2.5 -999 -999 -999 -999 -999 -999 7 1 3 5 4 4 2 12.1 3 4.2 4.7 3.5 2.4 -999 -999 -999 -999 -999 -999 7 1 3 5 4 4 2 11.4 2.6 3.6 4.3 3 2.3 -999 -999 -999 -999 -999 -999 7 1 3 5 4 4 2 11 2.4 3.4 3.5 2.8 2 -999 -999 -999 -999 -999 -999 7 1 3 5 4 4 2 10.7 2.5 3.4 3.8 3 2.2 -999 -999 -999 -999 -999 -999 7 1 3 5 4 4 2 10.5 3 3.5 4.3 3.2 2.3 -999 -999 -999 -999 -999 -999 7 1 3 5 4 4 2 10.8 2.7 3.6 4.1 3 2.2 -999 -999 -999 -999 -999 -999 7 1 3 5 4 4 2 11.5 2.8 4 4.4 3 2.3 -999 -999 -999 -999 -999 -999 7 1 3 5 4 4 2 12 2.6 3.9 3.9 2.8 2.2 -999 -999 -999 -999 -999 -999 7 1 3 5 4 4 2 12.3 3.2 4.1 4.3 3 2.3 -999 -999 -999 -999 -999 -999 7 1 3 5 4 4 2 12.5 3.3 4 4.5 2.7 2.5 -999 -999 -999 -999 -999 -999 7 1 3 5 4 4 2 10.9 2.5 3.6 4 2.6 2.1 -999 -999 -999 -999 -999 -999 7 1 3 5 4 4 2 11.6 3 3.8 4.5 3.2 2.4 -999 -999 -999 -999 -999 -999 7 1 3 5 4 4 2 12 2.8 4 4.4 2.7 2.3 -999 -999 -999 -999 -999 -999 7 1 3 5 4 4 2 9.8 2.7 3.6 4.2 3 2.2 -999 -999 -999 -999 -999 -999 7 1 3 5 4 4 2 9.4 2.7 3.5 3.8 2.7 2 -999 -999 -999 -999 -999 -999 7 1 3 5 4 4 2 11.8 3 4 4.3 3.2 2.3 -999 -999 -999 -999 -999 -999 7 1 3 5 4 4 2 11.3 2.7 4 4.3 3.1 2.3 -999 -999 -999 -999 -999 -999 7 1 3 5 4 4 2 10.5 2.5 3.6 3.9 3 2.1 -999 -999 -999 -999 -999 -999 7 1 3 5 4 4 2 11.7 2.9 4 4.2 3 2.2 -999 -999 -999 -999 -999 -999 7 1 3 5 4 4 2 10.1 3 3.7 4 2.7 2.1 -999 -999 -999 -999 -999 -999 7 1 3 5 4 4 2 10.7 2.5 3.9 4 2.7 2.1 -999 -999 -999 -999 -999 -999 7 1 3 5 4 4 2 12.1 3.7 4.1 4.5 3.1 2.3 -999 -999 -999 -999 -999 -999 7 1 3 5 4 4 2 10.5 3.7 3.6 4.2 2.7 2.1 -999 -999 -999 -999 -999 -999 7 1 3 5 4 4 2 11 3 3.8 4 2.8 2.1 -999 -999 -999 -999 -999 -999 7 1 3 5 4 4 2 11.8 3 3.8 4.2 3 2.3 -999 -999 -999 -999 -999 -999 7 1 3 5 4 4 2 12 2.8 4 4.1 3.1 2.3 -999 -999 -999 -999 -999 -999 7 1 3 5 4 4 2 12.3 2.7 4.1 4.4 3 2.2 -999 -999 -999 -999 -999 -999 7 1 3 5 4 4 2 12.5 3 4.2 4.6 3.2 2.5 -999 -999 -999 -999 -999 -999 7 1 3 5 4 4 2 11.5 2.8 3.5 3.8 3 2.2 -999 -999 -999 -999 -999 -999 7 1 3 5 4 4 2 12.2 3 4 4.3 3 2.4 -999 -999 -999 -999 -999 -999 7 1 3 5 4 4 2 11.8 2.6 3.9 4 3 2.2 -999 -999 -999 -999 -999 -999 7 1 3 5 4 4 2 12 2.7 4 3.9 2.7 2.2 -999 -999 -999 -999 -999 -999 7 1 3 5 4 4 2 11.6 2.6 3.8 4 2.7 2.2 -999 -999 -999 -999 -999 -999 7 1 3 5 4 4 2 12 3.2 8 4.7 3 2.4 -999 -999 -999 -999 -999 -999 7 1 3 5 4 4 2 10.5 2.6 3.6 3.7 2.5 2 -999 -999 -999 -999 -999 -999 7 1 3 5 4 4 2 10.6 2.2 3.3 3.7 2.5 2 -999 -999 -999 -999 -999 -999 7 1 3 5 4 4 2 10.3 2.4 3.2 3.5 2.2 2 -999 -999 -999 -999 -999 -999 Electronic Supplements to: Sukhodolskaya and Saveliev, Periodicum Biologorum, 2016, 118(3):273-280 DOI: 10.18054/pb.2016.118.3.3918 7 1 3 5 4 4 2 11.6 2.7 3.8 4.1 2.8 2.1 -999 -999 -999 -999 -999 -999 7 1 3 5 4 4 2 12.3 2.8 4.1 4.4 3.2 2.4 -999 -999 -999 -999 -999 -999 7 1 3 5 4 4 2 11.1 3 4 4.3 2.8 2.1 -999 -999 -999 -999 -999 -999 7 1 3 5 4 4 2 10.6 2.3 3.7 4 3 2.1 -999 -999 -999 -999 -999 -999 7 1 3 5 4 4 2 10.5 2.6 3.8 4 2.8 2.2 -999 -999 -999 -999 -999 -999 7 1 3 5 4 4 2 10.6 2.7 3.6 4.1 3 2.1 -999 -999 -999 -999 -999 -999 7 1 3 5 4 4 2 10.3 2.8 3.7 3.8 3 2.2 -999 -999 -999 -999 -999 -999 7 1 3 5 4 4 2 11 2.5 3.8 3.6 2.9 2.1 -999 -999 -999 -999 -999 -999 7 1 3 5 4 4 2 12.1 3.1 4.1 4.6 3.3 2.4 -999 -999 -999 -999 -999 -999 7 1 3 5 4 4 2 10.1 2.4 3.6 3.7 2.8 1.8 -999 -999 -999 -999 -999 -999 7 1 3 5 4 4 2 10.2 2.5 4 4.2 3.2 2.2 -999 -999 -999 -999 -999 -999 7 1 3 5 4 4 2 11 2.6 3.7 4.1 3 2.3 -999 -999 -999 -999 -999 -999 7 1 3 5 4 4 2 12.7 3.1 3.2 4.4 2.8 2.4 -999 -999 -999 -999 -999 -999 7 1 3 5 4 4 2 11.8 2.8 3.8 4.5 3.1 2.3 -999 -999 -999 -999 -999 -999 7 1 3 5 4 4 2 10.4 2.3 3.5 3.7 2.8 1.9 -999 -999 -999 -999 -999 -999 7 1 3 5 4 4 2 10.5 2.4 3.5 3.7 2.7 2.1 -999 -999 -999 -999 -999 -999 7 1 3 5 4 4 2 10.5 2.5 3.7 4.1 3 2.2 -999 -999 -999 -999 -999 -999 7 1 3 5 4 4 2 11 2.8 3.5 4 2.8 2.2 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 10.8 2.8 3.8 4.3 2.7 2.3 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 9.6 2.6 3.6 3.7 2.6 2.3 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 11.5 3.5 4.5 4.7 3.2 2.7 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 11.3 3.5 4.5 4.7 3.2 2.7 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 9.9 3.5 4 4.1 3.2 2.5 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 11.1 2.8 3.7 3.9 2.7 2.2 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 10.3 2.7 3.7 4 3 2.3 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 11.00 2.70 3.70 4.00 3.00 2.30 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 10.40 2.60 3.50 3.70 2.90 2.20 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 11.30 2.70 3.70 4.00 3.00 2.30 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 10.70 2.60 3.60 4.00 3.00 2.30 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 11.10 2.70 3.60 4.00 2.70 2.30 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 11.1 2.6 3.6 3.9 2.8 2.3 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 10.5 2.8 3.5 3.9 2.6 2.2 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 10.30 2.50 3.60 4.00 2.70 2.20 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 9.50 2.60 3.40 3.40 2.60 2.00 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 10.00 2.20 3.70 3.70 2.70 2.20 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 10.40 2.50 3.30 3.70 2.50 2.10 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 8.20 2.20 3.00 3.30 2.30 1.90 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 10.00 2.40 3.20 3.40 2.00 1.80 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 11.1 2.8 3.9 4.1 2.8 2.3 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 10.5 2.9 3.3 3.8 2.5 2.3 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 11.2 2.7 4 4.3 3.2 2.5 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 8.8 2.4 3.2 3.4 2.3 2.1 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 10.9 2.8 3.9 4.1 3.2 2.5 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 9.5 2.7 3.5 3.8 2.2 2.1 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 8.6 2.3 3.4 3.4 2.6 2.5 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 11.2 3 3.8 4 2.8 2.3 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 10.3 2.8 3.8 4 2.8 2.5 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 10.3 3 3.5 4 2.7 2.4 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 9.3 2.6 3.5 3.8 2.6 2 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 9.5 2.3 3.2 3.4 2.5 2 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 10.4 2.5 3.3 3.7 2.6 2.2 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 10.7 2.5 3.4 3.9 2.6 2.2 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 11.3 2.9 3.7 4.5 2.7 2.4 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 10.5 2.6 3.2 3.4 2.7 2.2 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 10.7 2.4 3.4 3.8 2.8 2.1 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 11.2 2.3 3.7 4 2.6 2.1 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 10.1 3.3 3.5 3.9 2.5 2.2 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 10.2 2.3 3.3 3.8 2.3 2.1 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 10 2.2 3.5 3.6 2.6 2.2 -999 -999 -999 -999 -999 -999 Electronic Supplements to: Sukhodolskaya and Saveliev, Periodicum Biologorum, 2016, 118(3):273-280 DOI: 10.18054/pb.2016.118.3.3918 7 1 3 3 4 4 3 9.8 2.3 3.5 3.3 2.3 2.1 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 10.1 2.7 3.4 3.5 2.3 2 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 10.2 3.2 3.3 3.7 2.5 2 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 11.2 2.7 4 4.3 3.2 2.5 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 8.6 2.3 3.4 3.4 2.6 2.5 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 11.1 2.7 3.6 4.1 2.6 2.2 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 10.3 2.5 3.5 3.8 2.7 2.2 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 11.2 2.7 3.8 3.9 3 2.5 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 9.4 2.2 3.2 3.4 2.4 1.9 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 10.8 2.8 3.8 4.3 2.7 2.3 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 9.6 2.6 3.6 3.7 2.6 2.3 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 11.5 3.5 4.5 4.7 3.2 2.7 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 11.3 3.5 4.5 4.7 3.2 2.7 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 9.9 3.5 4 4.1 3.2 2.5 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 11.1 2.8 3.7 3.9 2.7 2.2 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 10.3 2.7 3.7 4 3 2.3 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 11.1 2.8 3.9 4.1 2.8 2.3 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 10.5 2.9 3.3 3.8 2.5 2.3 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 11.2 2.7 4 4.3 3.2 2.5 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 8.8 2.4 3.2 3.4 2.3 2.1 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 11 2.7 3.7 4 3 2.3 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 10.4 2.6 3.5 3.7 2.9 2.2 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 11.3 2.7 3.7 4 3 2.3 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 10.7 2.6 3.6 4 3 2.3 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 11.1 2.7 3.6 4 2.7 2.3 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 11.1 2.6 3.6 3.9 2.8 2.3 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 10.5 2.8 3.5 3.9 2.6 2.2 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 10.3 2.5 3.6 4 2.7 2.2 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 9.5 2.6 3.4 3.4 2.6 2 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 10 2.2 3.7 3.7 2.7 2.2 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 10.4 2.5 3.3 3.7 2.5 2.1 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 8.2 2.2 3 3.3 2.3 1.9 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 10 2.4 3.2 3.4 2 1.8 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 10.9 2.8 3.9 4.1 3.2 2.5 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 9.5 2.7 3.5 3.8 2.2 2.1 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 8.6 2.3 3.4 3.4 2.6 2.5 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 11.2 3 3.8 4 2.8 2.3 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 10.3 2.8 3.8 4 2.8 2.5 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 10.3 3 3.5 4 2.7 2.4 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 9.3 2.6 3.5 3.8 2.6 2 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 9.5 2.3 3.2 3.4 2.5 2 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 10.4 2.5 3.3 3.7 2.6 2.2 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 10.7 2.5 3.4 3.9 2.6 2.2 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 11.3 2.9 3.7 4.5 2.7 2.4 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 10.5 2.6 3.2 3.4 2.7 2.2 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 10.7 2.4 3.4 3.8 2.8 2.1 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 11.2 2.3 3.7 4 2.6 2.1 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 10.1 3.3 3.5 3.9 2.5 2.2 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 10.2 2.3 3.3 3.8 2.3 2.1 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 10 2.2 3.5 3.6 2.6 2.2 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 9.8 2.3 3.5 3.3 2.3 2.1 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 10.1 2.7 3.4 3.5 2.3 2 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 10.2 3.2 3.3 3.7 2.5 2 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 11.2 2.7 4 4.3 3.2 2.5 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 8.6 2.3 3.4 3.4 2.6 2.5 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 11.1 2.7 3.6 4.1 2.6 2.2 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 10.3 2.5 3.5 3.8 2.7 2.2 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 11.2 2.7 3.8 3.9 3 2.5 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 9.4 2.2 3.2 3.4 2.4 1.9 -999 -999 -999 -999 -999 -999 Electronic Supplements to: Sukhodolskaya and Saveliev, Periodicum Biologorum, 2016, 118(3):273-280 DOI: 10.18054/pb.2016.118.3.3918 7 1 5 7 1 2 3 11.5 3 4 4.2 3.5 2.5 -999 -999 -999 -999 -999 -999 7 1 5 7 1 2 3 11.1 2.4 3.8 3.7 3.1 2.1 -999 -999 -999 -999 -999 -999 7 1 5 7 1 2 3 10.2 2.2 3.4 3.5 2.8 2 -999 -999 -999 -999 -999 -999 7 1 5 7 1 2 3 10.4 2.5 3.6 3.7 3 2 -999 -999 -999 -999 -999 -999 7 1 5 7 1 2 3 11 2.6 3.9 4 3.2 2.2 -999 -999 -999 -999 -999 -999 7 1 5 7 1 2 3 10.3 2.3 3.5 3.6 2.8 2 -999 -999 -999 -999 -999 -999 7 1 5 7 1 2 3 10.2 2.4 3.6 4 3.2 2.2 -999 -999 -999 -999 -999 -999 7 1 5 7 1 2 3 10.8 2.6 3.7 3.7 3.4 2.3 -999 -999 -999 -999 -999 -999 7 1 5 7 1 2 3 10.4 2.5 3.6 3.8 2.9 2.3 -999 -999 -999 -999 -999 -999 7 1 5 7 1 2 3 11.5 2.5 3.8 4.2 3 2.6 -999 -999 -999 -999 -999 -999 7 1 5 7 1 2 3 11.9 3 3.5 4.1 3.3 2.3 -999 -999 -999 -999 -999 -999 7 1 5 7 1 2 3 10.6 2.4 3.6 3.7 2.8 2.3 -999 -999 -999 -999 -999 -999 7 1 5 7 1 2 3 10.7 2.4 3.5 3.8 2.7 2.2 -999 -999 -999 -999 -999 -999 7 1 5 7 1 2 3 11.2 2.3 3.2 3.5 3.1 2.2 -999 -999 -999 -999 -999 -999 7 1 5 7 1 2 3 9.3 2 3.1 3.5 2.7 1.8 -999 -999 -999 -999 -999 -999 7 1 5 7 1 2 3 11.1 2.5 3.7 4 2.9 2.3 -999 -999 -999 -999 -999 -999 7 1 5 7 1 2 3 10.3 2.4 3.6 3.7 2.7 2.1 -999 -999 -999 -999 -999 -999 7 1 5 7 1 2 3 11.7 2.8 4.2 4.4 3.4 2.4 -999 -999 -999 -999 -999 -999 7 1 5 7 1 2 3 10.1 2.3 3.7 4 3 2.2 -999 -999 -999 -999 -999 -999 7 1 5 7 1 2 3 10.2 2.6 3.8 4.3 3.2 2.3 -999 -999 -999 -999 -999 -999 7 1 4 4 2 4 3 10.5 2.9 3.9 4 2.6 2.5 -999 -999 -999 -999 -999 -999 7 1 4 4 2 4 3 10.7 2.6 3.7 3.9 3 2.5 -999 -999 -999 -999 -999 -999 7 1 4 4 2 4 3 11.3 2.5 3.7 4.3 3.1 2.3 -999 -999 -999 -999 -999 -999 7 1 4 4 2 4 3 10.3 2.6 3.6 4 3 2.5 -999 -999 -999 -999 -999 -999 7 1 4 4 2 4 3 11.2 2.7 3.7 3.9 3 2.3 -999 -999 -999 -999 -999 -999 7 1 4 4 2 4 3 9.5 2.3 2.8 3.3 2.2 2 -999 -999 -999 -999 -999 -999 7 1 4 4 2 4 3 10.4 2.5 3.2 3.8 2.8 2.5 -999 -999 -999 -999 -999 -999 7 1 4 4 2 4 3 10.5 2.6 3.4 3.7 2.9 2.1 -999 -999 -999 -999 -999 -999 7 1 4 4 2 4 3 10.7 2.3 3.3 4 3 2.3 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 11.2 2.6 4 4.3 2.6 2.4 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 12.1 2.7 4.3 4.6 3 2.2 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 11 2.5 4.1 4.3 3.1 2.5 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 10.8 2.4 3.5 4 2.8 2.2 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 12 2.6 3.9 4.6 2.8 2.3 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 11.9 3.1 4 5 3 2.3 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 12.6 3 4.3 4.3 3 2.3 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 11.6 2.7 3.9 4.3 2.9 2.2 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 10.8 2.5 3.9 4.2 2.8 2.1 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 11.9 2.8 4 4.4 2.9 2.2 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 11.9 3.2 4.2 4.5 3.1 2.4 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 11.3 3.2 4.2 4.1 3.2 2.4 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 11 3 3.6 4.3 3.2 2.3 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 9 2.3 3.2 3.3 2.1 2 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 11.6 3.4 4.1 4.4 3.3 2.5 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 10.9 2.8 3.9 4.1 2.7 2.6 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 11.5 3.1 4 4.5 3 2.5 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 11.9 2.8 4 4.1 3.2 2.3 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 11.5 2.5 4 4.1 2.8 2.1 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 10.8 2.4 3.8 3.9 2.8 2.1 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 10.7 2.5 3.9 3.8 2.7 2.1 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 10.6 2.2 3.9 4 2.6 2 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 10.8 2.5 3.6 4 2.4 2.2 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 10 2.3 3.6 3.7 2.7 1.8 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 11 2.7 3.7 4.2 2.4 2.1 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 10.1 2.4 3.6 3.7 2.3 1.8 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 11.2 2.7 3.9 4.3 2.7 2.1 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 10.5 2.5 3.8 3.8 2.5 2 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 10.6 2.5 3.7 4.1 2.4 2.1 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 10.7 2.4 3.8 4.1 2.5 2.3 -999 -999 -999 -999 -999 -999 Electronic Supplements to: Sukhodolskaya and Saveliev, Periodicum Biologorum, 2016, 118(3):273-280 DOI: 10.18054/pb.2016.118.3.3918 7 1 3 5 2 4 2 10.7 2.2 3.8 4 2.5 2.3 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 10.9 2.3 3.6 3.9 2 2 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 11 2.2 3.5 3.8 2.4 2.1 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 10.4 2.5 3.4 3.8 2.2 2 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 12.2 2.7 4 4.4 2.7 2.2 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 11.2 2.6 4 4 2.8 2.1 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 10.3 2.3 3.5 3.6 2.4 2 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 11.2 2.4 3.6 4 2.5 2 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 11.3 2.5 3.7 4.2 2.8 2 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 11.4 2.8 3.8 4.1 2.7 2.2 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 11 2.4 3.7 3.8 2.4 2 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 10.5 2.6 3.9 4 2.6 2.2 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 10 2.4 3.6 3.7 2.3 2.1 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 13.3 3.4 4.2 4.8 3.4 2.7 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 10 2.7 3.5 3.7 2.4 2.1 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 12.2 3 4.3 4.6 3.1 2.6 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 11.8 3.1 4 4.5 3.1 2.6 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 11.9 3.3 4.4 4.5 3.3 2.7 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 13 3.7 4.5 5 3.7 2.5 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 11.9 3 4.1 4.5 3 2.7 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 10.7 2.5 4 4 2.9 2.4 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 10.7 2.8 3.8 4.1 2.7 2.5 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 10.9 2.9 3.7 4.1 2.8 2.5 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 12.8 3.2 4.6 5 3.6 2.6 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 10.7 2.9 3.9 4.8 3 2.5 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 11.7 2.4 3.6 4.1 2.7 2.5 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 12 3.2 4 4.5 3 2.5 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 11.1 2.8 3.7 4 2.6 3 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 11.3 3 3.9 4.3 3.1 2.3 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 11.2 2.7 3.7 4.3 2.8 2.4 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 11.7 2.7 4 4.5 2.8 2.4 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 10.2 2.5 3.5 3.9 2.5 2 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 10.7 3 3.8 4.4 3 2.3 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 11.7 2.7 3.9 4.2 2.8 2.2 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 11.5 2.6 4 4.2 2.7 2.2 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 10.8 2.5 3.8 4 2.5 2.1 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 11.7 2.5 3.8 4.2 2.3 2.1 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 11.9 2.4 4 4.4 2.8 2.1 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 11 2.7 3.8 4 2.5 2.1 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 10.8 2.5 3.6 3.8 2.4 2.3 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 11 2.5 3.8 3.8 2.8 2.1 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 11.5 2.8 4.1 4.3 3 2.4 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 11.9 2.6 4.1 4 3.2 2.5 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 12 3.1 4.1 4.7 3.2 2.3 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 12.5 3 4.1 4.9 3.3 2.3 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 12.3 3.2 4.2 4.8 3.3 2.3 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 11.7 3.1 3.7 4.5 3 2.2 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 12 2.6 4.1 4.6 2.9 2.2 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 11.7 2.8 3.1 4.5 2.8 2.3 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 11.6 2.6 3.8 4.3 2.7 2.4 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 11.3 3.4 3.5 4.5 2.7 2.1 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 11.9 2.7 3.5 4.3 2.6 2.4 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 11 3 3.7 4.2 2 1.9 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 11 3.1 3.7 4.5 2 2.4 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 11.6 3.1 3.9 4.4 1.7 2.3 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 10.5 3.1 4 4.2 2 2.3 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 10.5 3.2 4 4.3 2 2.2 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 11.6 3.1 3.9 4.5 2 2.2 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 10 2.5 4.2 4.2 2.5 2.3 -999 -999 -999 -999 -999 -999 Electronic Supplements to: Sukhodolskaya and Saveliev, Periodicum Biologorum, 2016, 118(3):273-280 DOI: 10.18054/pb.2016.118.3.3918 7 1 3 5 2 4 2 9.8 2.5 4.2 4.2 2.5 2.3 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 9.5 2.5 4 4 2.5 2.5 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 10.5 2.7 4.1 4.1 2.5 2.2 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 9.9 2.6 4.1 4.1 2.3 2.5 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 10 2.5 4.1 4 2.7 2 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 10 2.5 4 4 2.6 2.2 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 10 2.6 4 4.1 2.5 2.3 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 10.5 2.7 4 4 2.5 2.5 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 9.5 2.6 4.1 4.1 2.7 2.1 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 10 2.7 4.2 4 2.5 2.2 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 11 2.5 4.2 4.2 2.6 2.5 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 10.5 2.6 4.1 4.3 2.5 2.1 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 10 2.5 4.2 4 2.6 2.3 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 11 2.5 3.7 3.6 2.6 2.3 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 12.6 3.2 4 4.5 2.8 2.4 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 10.5 2.7 3.8 4.2 3 2.2 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 11.1 2.6 4.1 4.3 3.4 2.3 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 11.5 3 4 4.2 2.7 2.1 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 12 3.3 4.1 4.2 3.3 2.4 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 9.9 2.2 3.2 3.9 1.5 2.3 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 10 2.5 4 3.9 1.5 2.2 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 9.5 2.2 3.5 3.9 1.7 2.3 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 9.5 2.3 3.6 4 1.6 2.5 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 9.3 2.2 3.6 3.8 1.6 2.3 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 9 2.3 3.6 4 1.7 2.2 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 10.6 2.6 4 4.4 2.8 2.3 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 12.1 2.5 3.6 4.3 2.3 2.4 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 9.2 2.3 3.5 3.8 2.5 2.2 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 10.3 2.4 3.6 3.7 2.6 2 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 10.6 2.6 3.7 4.1 2.8 2.1 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 9.8 2.2 3.5 3.7 2.3 2 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 10.5 2.4 3.9 3.9 2.7 2.2 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 11.2 2.8 3.7 3.7 3.2 2 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 11.3 2.6 3.8 4.1 2.9 2.1 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 10.9 3 4 4.1 3.1 2.4 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 10 3 3.4 4 2.5 2.4 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 12.2 2.8 4.2 4.3 2.8 2.4 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 12 2.5 4 4.3 3.2 2.3 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 11.6 2.6 3.8 4.1 3 2.2 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 11 3.2 4 4.3 3.1 2.6 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 12.1 2.8 3.9 3.7 3.2 2.2 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 11.9 3.4 4.2 4.6 3.3 2.2 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 12.3 3.1 4.2 4.8 3.2 2.5 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 10.5 2.5 4 4 3 2.1 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 12.7 3.2 4 4.3 2.8 2.5 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 10.9 2.6 3.6 3.9 2.6 2 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 11.4 2.8 3.6 3.8 2.8 2.2 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 11.6 3 3.8 4 2.7 2.1 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 11.8 3 4 4.5 3 2.3 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 11.3 3.2 3.9 4.1 2.7 2.3 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 11.4 2.5 3.9 4 2.7 2.2 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 10.6 2.3 3.7 3.7 3.2 2.1 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 11.2 2.6 3.8 4 2.8 2.3 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 11.3 2.6 3.8 3.6 2.7 2.3 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 11 2.5 3.7 3.6 2.6 2.3 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 12.6 3.2 4 4.5 2.8 2.4 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 10.5 2.7 3.8 4.2 3 2.2 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 11.1 2.6 4.1 4.3 3.4 2.3 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 11.5 3 4 4.2 2.7 2.1 -999 -999 -999 -999 -999 -999 Electronic Supplements to: Sukhodolskaya and Saveliev, Periodicum Biologorum, 2016, 118(3):273-280 DOI: 10.18054/pb.2016.118.3.3918 7 1 3 3 4 4 3 12 3.3 4.1 4.2 3.3 2.4 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 9.9 2.2 3.2 3.9 1.5 2.3 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 10 2.5 4 3.9 1.5 2.2 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 9.5 2.2 3.5 3.9 1.7 2.3 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 9.5 2.3 3.6 4 1.6 2.5 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 9.3 2.2 3.6 3.8 1.6 2.3 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 9 2.3 3.6 4 1.7 2.2 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 10.6 2.6 4 4.4 2.8 2.3 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 12.1 2.5 3.6 4.3 2.3 2.4 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 9.2 2.3 3.5 3.8 2.5 2.2 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 10.3 2.4 3.6 3.7 2.6 2 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 10.6 2.6 3.7 4.1 2.8 2.1 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 9.8 2.2 3.5 3.7 2.3 2 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 10.5 2.4 3.9 3.9 2.7 2.2 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 10.5 2.5 3.8 4 2.5 2.3 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 10.2 2.3 3.6 3.9 1.8 2.2 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 11.4 2.3 4 4.5 1.7 2.5 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 10.8 2.5 4.1 4.4 1.5 2.5 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 11.2 2.7 3.6 4.3 2.7 2.2 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 11.3 2.8 4.1 4.2 2.8 2.4 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 11.6 2.5 3.8 4.1 2.7 2.1 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 10.7 2.6 3.7 4.3 2.7 2.2 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 10.8 2.5 3.6 3.7 2.2 2.1 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 11.3 2.3 3.6 3.5 2.6 2 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 10 2.7 3.6 4.2 2.8 2.2 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 10.6 2.4 3.4 3.8 2.2 1.9 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 10.3 2.6 3.7 3.8 2.7 2.2 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 11 2.5 3.4 3.9 2.3 2 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 11 2.5 3.6 4 2.7 2.2 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 11.2 2.8 3.7 3.7 3.2 2 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 11.3 2.6 3.8 4.1 2.9 2.1 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 10.9 3 4 4.1 3.1 2.4 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 10 3 3.4 4 2.5 2.4 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 12.2 2.8 4.2 4.3 2.8 2.4 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 12 2.5 4 4.3 3.2 2.3 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 11.6 2.6 3.8 4.1 3 2.2 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 11 3.2 4 4.3 3.1 2.6 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 12.1 2.8 3.9 3.7 3.2 2.2 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 11.9 3.4 4.2 4.6 3.3 2.2 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 12.3 3.1 4.2 4.8 3.2 2.5 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 10.5 2.5 4 4 3 2.1 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 12.7 3.2 4 4.3 2.8 2.5 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 10.9 2.6 3.6 3.9 2.6 2 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 11.4 2.8 3.6 3.8 2.8 2.2 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 11.6 3 3.8 4 2.7 2.1 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 11.8 3 4 4.5 3 2.3 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 11.3 3.2 3.9 4.1 2.7 2.3 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 11.4 2.5 3.9 4 2.7 2.2 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 10.6 2.3 3.7 3.7 3.2 2.1 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 11.2 2.6 3.8 4 2.8 2.3 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 11.3 2.6 3.8 3.6 2.7 2.3 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 10.5 2.5 3.8 4 2.5 2.3 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 10.2 2.3 3.6 3.9 1.8 2.2 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 11.4 2.3 4 4.5 1.7 2.5 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 10.8 2.5 4.1 4.4 1.5 2.5 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 11.2 2.7 3.6 4.3 2.7 2.2 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 11.3 2.8 4.1 4.2 2.8 2.4 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 11.6 2.5 3.8 4.1 2.7 2.1 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 10.7 2.6 3.7 4.3 2.7 2.2 -999 -999 -999 -999 -999 -999 Electronic Supplements to: Sukhodolskaya and Saveliev, Periodicum Biologorum, 2016, 118(3):273-280 DOI: 10.18054/pb.2016.118.3.3918 7 1 3 3 4 4 3 10.8 2.5 3.6 3.7 2.2 2.1 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 11.3 2.3 3.6 3.5 2.6 2 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 10 2.7 3.6 4.2 2.8 2.2 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 10.6 2.4 3.4 3.8 2.2 1.9 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 10.3 2.6 3.7 3.8 2.7 2.2 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 11 2.5 3.4 3.9 2.3 2 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 11 2.5 3.6 4 2.7 2.2 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 10.8 2.8 3.8 4.3 2.7 2.3 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 9.6 2.6 3.6 3.7 2.6 2.3 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 11.5 3.5 4.5 4.7 3.2 2.7 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 11.3 3.5 4.5 4.7 3.2 2.7 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 9.9 3.5 4 4.1 3.2 2.5 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 11.1 2.8 3.7 3.9 2.7 2.2 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 10.3 2.7 3.7 4 3 2.3 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 11.00 2.70 3.70 4.00 3.00 2.30 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 10.40 2.60 3.50 3.70 2.90 2.20 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 11.30 2.70 3.70 4.00 3.00 2.30 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 10.70 2.60 3.60 4.00 3.00 2.30 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 11.10 2.70 3.60 4.00 2.70 2.30 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 11.1 2.6 3.6 3.9 2.8 2.3 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 10.5 2.8 3.5 3.9 2.6 2.2 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 10.30 2.50 3.60 4.00 2.70 2.20 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 9.50 2.60 3.40 3.40 2.60 2.00 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 10.00 2.20 3.70 3.70 2.70 2.20 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 10.40 2.50 3.30 3.70 2.50 2.10 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 8.20 2.20 3.00 3.30 2.30 1.90 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 10.00 2.40 3.20 3.40 2.00 1.80 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 11.1 2.8 3.9 4.1 2.8 2.3 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 10.5 2.9 3.3 3.8 2.5 2.3 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 11.2 2.7 4 4.3 3.2 2.5 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 8.8 2.4 3.2 3.4 2.3 2.1 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 10.9 2.8 3.9 4.1 3.2 2.5 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 9.5 2.7 3.5 3.8 2.2 2.1 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 8.6 2.3 3.4 3.4 2.6 2.5 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 11.2 3 3.8 4 2.8 2.3 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 10.3 2.8 3.8 4 2.8 2.5 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 10.3 3 3.5 4 2.7 2.4 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 9.3 2.6 3.5 3.8 2.6 2 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 9.5 2.3 3.2 3.4 2.5 2 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 10.4 2.5 3.3 3.7 2.6 2.2 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 10.7 2.5 3.4 3.9 2.6 2.2 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 11.3 2.9 3.7 4.5 2.7 2.4 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 10.5 2.6 3.2 3.4 2.7 2.2 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 10.7 2.4 3.4 3.8 2.8 2.1 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 11.2 2.3 3.7 4 2.6 2.1 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 10.1 3.3 3.5 3.9 2.5 2.2 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 10.2 2.3 3.3 3.8 2.3 2.1 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 10 2.2 3.5 3.6 2.6 2.2 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 9.8 2.3 3.5 3.3 2.3 2.1 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 10.1 2.7 3.4 3.5 2.3 2 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 10.2 3.2 3.3 3.7 2.5 2 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 11.2 2.7 4 4.3 3.2 2.5 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 8.6 2.3 3.4 3.4 2.6 2.5 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 11.1 2.7 3.6 4.1 2.6 2.2 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 10.3 2.5 3.5 3.8 2.7 2.2 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 11.2 2.7 3.8 3.9 3 2.5 -999 -999 -999 -999 -999 -999 7 1 3 3 4 4 3 9.4 2.2 3.2 3.4 2.4 1.9 -999 -999 -999 -999 -999 -999 7 1 5 7 1 2 3 11.5 3 4 4.2 3.5 2.5 -999 -999 -999 -999 -999 -999 7 1 5 7 1 2 3 11.1 2.4 3.8 3.7 3.1 2.1 -999 -999 -999 -999 -999 -999 Electronic Supplements to: Sukhodolskaya and Saveliev, Periodicum Biologorum, 2016, 118(3):273-280 DOI: 10.18054/pb.2016.118.3.3918 7 1 5 7 1 2 3 10.2 2.2 3.4 3.5 2.8 2 -999 -999 -999 -999 -999 -999 7 1 5 7 1 2 3 10.4 2.5 3.6 3.7 3 2 -999 -999 -999 -999 -999 -999 7 1 5 7 1 2 3 11 2.6 3.9 4 3.2 2.2 -999 -999 -999 -999 -999 -999 7 1 5 7 1 2 3 10.3 2.3 3.5 3.6 2.8 2 -999 -999 -999 -999 -999 -999 7 1 5 7 1 2 3 10.2 2.4 3.6 4 3.2 2.2 -999 -999 -999 -999 -999 -999 7 1 5 7 1 2 3 10.8 2.6 3.7 3.7 3.4 2.3 -999 -999 -999 -999 -999 -999 7 1 5 7 1 2 3 10.4 2.5 3.6 3.8 2.9 2.3 -999 -999 -999 -999 -999 -999 7 1 5 7 1 2 3 11.5 2.5 3.8 4.2 3 2.6 -999 -999 -999 -999 -999 -999 7 1 5 7 1 2 3 11.9 3 3.5 4.1 3.3 2.3 -999 -999 -999 -999 -999 -999 7 1 5 7 1 2 3 10.6 2.4 3.6 3.7 2.8 2.3 -999 -999 -999 -999 -999 -999 7 1 5 7 1 2 3 10.7 2.4 3.5 3.8 2.7 2.2 -999 -999 -999 -999 -999 -999 7 1 5 7 1 2 3 11.2 2.3 3.2 3.5 3.1 2.2 -999 -999 -999 -999 -999 -999 7 1 5 7 1 2 3 9.3 2 3.1 3.5 2.7 1.8 -999 -999 -999 -999 -999 -999 7 1 5 7 1 2 3 11.1 2.5 3.7 4 2.9 2.3 -999 -999 -999 -999 -999 -999 7 1 5 7 1 2 3 10.3 2.4 3.6 3.7 2.7 2.1 -999 -999 -999 -999 -999 -999 7 1 5 7 1 2 3 11.7 2.8 4.2 4.4 3.4 2.4 -999 -999 -999 -999 -999 -999 7 1 5 7 1 2 3 10.1 2.3 3.7 4 3 2.2 -999 -999 -999 -999 -999 -999 7 1 5 7 1 2 3 10.2 2.6 3.8 4.3 3.2 2.3 -999 -999 -999 -999 -999 -999 7 1 4 4 4 4 3 10.5 2.9 3.9 4 2.6 2.5 -999 -999 -999 -999 -999 -999 7 1 4 4 4 4 3 10.7 2.6 3.7 3.9 3 2.5 -999 -999 -999 -999 -999 -999 7 1 4 4 4 4 3 11.3 2.5 3.7 4.3 3.1 2.3 -999 -999 -999 -999 -999 -999 7 1 4 4 4 4 3 10.3 2.6 3.6 4 3 2.5 -999 -999 -999 -999 -999 -999 7 1 4 4 4 4 3 11.2 2.7 3.7 3.9 3 2.3 -999 -999 -999 -999 -999 -999 7 1 4 4 4 4 3 9.5 2.3 2.8 3.3 2.2 2 -999 -999 -999 -999 -999 -999 7 1 4 4 4 4 3 10.4 2.5 3.2 3.8 2.8 2.5 -999 -999 -999 -999 -999 -999 7 1 4 4 4 4 3 10.5 2.6 3.4 3.7 2.9 2.1 -999 -999 -999 -999 -999 -999 7 1 4 4 4 4 3 10.7 2.3 3.3 4 3 2.3 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 9.7 2.1 3.5 3.6 3 2.1 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 9.3 2.1 3.2 3.3 2.7 1.8 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 10 2.3 3.6 3.9 2.8 2 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 9.1 2 3.3 3.5 2.5 1.8 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 10.6 2.6 3.7 4.1 3.2 2.3 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 11.3 2.5 3.9 4.2 3.1 2.2 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 12 2.7 4.1 4.6 3.2 2.3 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 11.1 2.6 3.6 3.8 3.2 2.1 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 10.4 2.6 3.6 3.9 2.8 2.1 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 10.2 2.5 3.4 3.7 3.1 2 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 12 3.1 4 4.5 3 2.5 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 11.3 2.7 3.7 4.2 3.3 2.3 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 10.2 2.6 3.4 3.8 2.9 2.2 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 10.9 2.6 3.5 4 2.8 2.1 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 10.5 2.4 3.5 3.6 2.6 2 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 10.6 2.6 3.7 4 2.7 2.1 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 11.4 2.8 3.8 4.1 2.9 2.3 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 11.1 2.7 3.3 4 2.89 2.2 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 10.3 2.4 3.4 3.9 2.7 2.1 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 12.4 3 3.5 4.6 3.3 2.4 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 10.2 2.6 3.5 4.2 2.8 2.1 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 10.7 2.4 3.7 3.7 3 2.1 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 10.1 2.6 3.6 4 2.8 2.2 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 10 2.5 3.2 4.1 2.7 2.1 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 11.2 2.8 3.8 4.2 3 2.2 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 10.9 2.6 3.6 4 2.8 2.1 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 10.5 2.7 3.5 3.9 2.5 2.3 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 11.3 2.8 3.5 4.3 2.9 2.2 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 10.4 2.5 3.5 3.8 2.5 1.9 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 11.3 2.8 3.8 4 3 2.2 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 9.3 2.3 3.4 3.9 2.5 2 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 9.4 2.6 3.5 3.6 2.7 1.9 -999 -999 -999 -999 -999 -999 Electronic Supplements to: Sukhodolskaya and Saveliev, Periodicum Biologorum, 2016, 118(3):273-280 DOI: 10.18054/pb.2016.118.3.3918 7 1 3 5 2 4 2 10.5 2.8 3.8 4 2.8 2.1 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 11.2 2.6 4 4.3 3 2.2 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 10.6 2.5 3.5 4.3 3 2.2 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 10.8 2.4 3.8 4.2 2.9 2.3 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 11.1 2.7 3.7 4.1 2.9 2.2 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 11 2.6 4 3.9 3.2 2.2 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 11 2.6 3.6 4.2 3 2.3 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 11.1 2.5 3.7 4.1 3 2.2 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 10.7 2.5 3.6 4 3 2.1 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 10.9 2.5 3.7 3.7 3.1 2.1 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 12 2.6 4 4.3 3.4 2.2 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 11.8 3.1 4 4.5 3.2 2.4 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 10.2 2.7 3.7 3.6 2.8 2.1 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 10.8 2.8 3.7 4 3.1 2 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 12.2 3.2 4.1 4.6 3 2.2 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 10.3 2.5 3.4 3.6 2.6 2 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 11.3 2.8 3.7 3.9 3 2.1 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 10.9 2.8 3.8 4.2 2.9 2.1 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 11.8 2.7 4 4.3 3 2.2 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 11 2.6 3.7 3.7 2.8 2.1 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 11 2.5 3.5 3.9 2.7 2.1 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 10.2 2.5 3.3 3.7 2.5 1.9 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 10.1 2.3 3.3 3.6 2.3 1.8 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 10.7 2.7 3.4 3.9 2.5 2.1 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 10.6 2.6 3.7 3.8 2.8 2.1 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 12 3 3.9 4.3 2.9 2.4 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 10.7 2.6 3.7 3.8 2.8 2.1 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 11.8 2.8 3.8 4.2 2.9 2.2 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 10.4 2.4 3.2 3.7 2.8 2.1 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 10.7 2.5 3.5 3.8 2.9 2 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 11.7 2.6 3.5 3.8 3.1 2.1 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 10.8 2.7 4 4.2 3.4 2.2 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 13.4 3.4 4.2 5.2 4.2 2.8 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 11.8 2.8 4.1 4.5 3.5 2.4 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 10.7 2.8 3.8 4.3 3.3 2.2 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 11.9 3 4 4.4 3.6 2.6 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 10.4 2.4 3.6 3.9 3.2 2.2 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 10.6 2.6 3.7 3.8 3.4 2.2 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 11.6 2.6 4 4.3 3.5 2.2 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 11.1 2.8 3.9 4 3.3 2.3 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 9.9 2.5 3.7 3.8 2.8 1.9 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 10.8 2.8 3.6 4.2 2.9 2.2 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 10.2 2.6 3.4 4.2 2.8 2.1 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 11.8 2.5 3.9 3.7 3.4 2 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 10.5 3 3.7 4.3 3 2.2 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 12 3.1 4 4.6 3.1 2.4 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 12.4 2.9 3.8 4.6 3 2.5 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 12.1 3 4.2 4.7 3.5 2.4 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 11.4 2.6 3.6 4.3 3 2.3 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 11 2.4 3.4 3.5 2.8 2 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 10.7 2.5 3.4 3.8 3 2.2 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 10.5 3 3.5 4.3 3.2 2.3 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 10.8 2.7 3.6 4.1 3 2.2 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 11.5 2.8 4 4.4 3 2.3 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 12 2.6 3.9 3.9 2.8 2.2 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 12.3 3.2 4.1 4.3 3 2.3 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 12.5 3.3 4 4.5 2.7 2.5 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 10.9 2.5 3.6 4 2.6 2.1 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 11.6 3 3.8 4.5 3.2 2.4 -999 -999 -999 -999 -999 -999 Electronic Supplements to: Sukhodolskaya and Saveliev, Periodicum Biologorum, 2016, 118(3):273-280 DOI: 10.18054/pb.2016.118.3.3918 7 1 3 5 2 4 2 12 2.8 4 4.4 2.7 2.3 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 9.8 2.7 3.6 4.2 3 2.2 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 9.4 2.7 3.5 3.8 2.7 2 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 11.8 3 4 4.3 3.2 2.3 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 11.3 2.7 4 4.3 3.1 2.3 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 10.5 2.5 3.6 3.9 3 2.1 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 11.7 2.9 4 4.2 3 2.2 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 10.1 3 3.7 4 2.7 2.1 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 10.7 2.5 3.9 4 2.7 2.1 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 12.1 3.7 4.1 4.5 3.1 2.3 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 10.5 3.7 3.6 4.2 2.7 2.1 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 11 3 3.8 4 2.8 2.1 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 11.8 3 3.8 4.2 3 2.3 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 12 2.8 4 4.1 3.1 2.3 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 12.3 2.7 4.1 4.4 3 2.2 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 12.5 3 4.2 4.6 3.2 2.5 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 11.5 2.8 3.5 3.8 3 2.2 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 12.2 3 4 4.3 3 2.4 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 11.8 2.6 3.9 4 3 2.2 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 12 2.7 4 3.9 2.7 2.2 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 11.6 2.6 3.8 4 2.7 2.2 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 12 3.2 8 4.7 3 2.4 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 10.5 2.6 3.6 3.7 2.5 2 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 10.6 2.2 3.3 3.7 2.5 2 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 10.3 2.4 3.2 3.5 2.2 2 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 11.6 2.7 3.8 4.1 2.8 2.1 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 12.3 2.8 4.1 4.4 3.2 2.4 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 11.1 3 4 4.3 2.8 2.1 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 10.6 2.3 3.7 4 3 2.1 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 10.5 2.6 3.8 4 2.8 2.2 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 10.6 2.7 3.6 4.1 3 2.1 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 10.3 2.8 3.7 3.8 3 2.2 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 11 2.5 3.8 3.6 2.9 2.1 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 12.1 3.1 4.1 4.6 3.3 2.4 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 10.1 2.4 3.6 3.7 2.8 1.8 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 10.2 2.5 4 4.2 3.2 2.2 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 11 2.6 3.7 4.1 3 2.3 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 12.7 3.1 3.2 4.4 2.8 2.4 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 11.8 2.8 3.8 4.5 3.1 2.3 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 10.4 2.3 3.5 3.7 2.8 1.9 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 10.5 2.4 3.5 3.7 2.7 2.1 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 10.5 2.5 3.7 4.1 3 2.2 -999 -999 -999 -999 -999 -999 7 1 3 5 2 4 2 11 2.8 3.5 4 2.8 2.2 -999 -999 -999 -999 -999 -999 7 2 12 18 2 4 3 10.8 4 3.6 3.7 2.6 2.3 8 8 1 -999 -999 -999 7 2 12 18 2 4 3 10 4.1 3.8 3.6 2.7 2 8 8 1 -999 -999 -999 7 2 12 18 2 4 3 10.2 4 3.5 4 2.4 2.2 8 8 1 -999 -999 -999 7 2 12 18 2 4 3 10 3.7 3.5 3.6 2.4 2.1 8 8 1 -999 -999 -999 7 2 12 18 2 4 3 10.3 4.2 3.7 3.7 3.2 2.5 6 8 1 -999 -999 -999 7 2 12 18 2 4 3 10.5 4 3.9 3.5 2.5 2.3 8 8 1 -999 -999 -999 7 2 12 18 2 4 3 9.2 4 3.5 3.6 2.3 2.4 8 8 1 -999 -999 -999 7 2 12 18 2 4 3 9.8 4 3.8 3.9 2.4 2.5 8 8 1 -999 -999 -999 7 2 12 18 2 4 3 11.1 4.5 3.7 4 2.8 2.2 8 8 1 -999 -999 -999 7 2 12 18 2 4 3 11 4.4 4 4.2 2.5 2.5 8 8 1 -999 -999 -999 7 2 12 18 2 4 3 11.3 4.2 4 4.2 2.8 2.5 8 8 1 -999 -999 -999 7 2 12 18 2 4 3 10.5 4 3.8 4 3 2 8 8 1 -999 -999 -999 7 2 12 18 2 4 3 10.8 4.2 3.7 4 2.5 2.2 8 8 1 -999 -999 -999 7 2 12 18 2 4 3 11 4.4 4 4.2 2.8 2.3 8 8 1 -999 -999 -999 7 2 12 18 2 4 3 9.8 3.8 3.6 3.4 2.4 2.4 8 8 1 -999 -999 -999 7 2 12 18 2 4 3 10.5 4.5 3.4 4.1 3 2.3 8 8 1 -999 -999 -999 Electronic Supplements to: Sukhodolskaya and Saveliev, Periodicum Biologorum, 2016, 118(3):273-280 DOI: 10.18054/pb.2016.118.3.3918 7 2 12 18 2 4 3 10.2 4.2 3.8 3.6 2.8 2.6 8 8 1 -999 -999 -999 7 2 12 18 2 4 3 10 4 3.8 3.8 2.5 2 8 8 1 -999 -999 -999 7 2 12 18 2 4 3 10.7 4.2 4.1 4 4.5 2.2 8 8 1 -999 -999 -999 7 2 12 18 2 4 3 9.2 3.4 3.5 3.5 2 2 7 7 1 -999 -999 -999 7 2 12 18 2 4 3 10.7 4.4 3.7 4 2.8 2.3 8 8 1 -999 -999 -999 7 2 12 18 2 4 3 11.3 4 3.8 4 2.5 2.2 8 8 1 -999 -999 -999 7 2 12 18 2 4 3 9.5 4 3.5 3.8 2.5 2.3 8 8 1 -999 -999 -999 7 2 12 18 2 4 3 10.4 4.2 3.8 4 2.5 2.2 7 7 1 -999 -999 -999 7 2 12 18 2 4 3 10 4 3.5 3.6 2.3 2 8 8 1 -999 -999 -999 7 2 12 18 2 4 3 10.2 4.1 3.8 4 2.3 2.3 8 8 1 -999 -999 -999 7 2 12 18 2 4 3 10.6 5 4 4.3 2.4 2.3 8 8 1 -999 -999 -999 7 2 12 18 2 4 3 10.5 4.2 4 4 2.8 2.1 8 8 2 -999 -999 -999 7 2 12 18 2 4 3 9.5 4 3.5 3.8 3.8 2 8 7 2 -999 -999 -999 7 2 12 18 2 4 3 9.6 4 3.5 3.5 2.4 2 8 8 2 -999 -999 -999 7 2 12 18 2 4 3 9 4 3.5 3.5 2.5 2 8 8 2 -999 -999 -999 7 2 12 18 2 4 3 9 4 3.5 3.5 2.3 2.3 8 8 2 -999 -999 -999 7 2 12 18 2 4 3 10.3 3.8 3.6 4 2.8 2.1 8 8 2 -999 -999 -999 7 2 12 18 2 4 3 10 4 3.7 3.7 2.8 2.1 8 8 2 -999 -999 -999 7 2 12 18 2 4 3 9.7 4 3.5 3.7 2.8 2.2 8 8 2 -999 -999 -999 7 2 12 18 2 4 3 10.1 4 3.9 4 2 2.2 8 8 2 -999 -999 -999 7 2 12 18 2 4 3 9.6 4 3.5 3.8 2.5 2 8 8 2 -999 -999 -999 7 2 12 18 2 4 3 9.5 4 3.6 3.3 2.5 2 8 8 2 -999 -999 -999 7 2 12 18 2 4 3 9.8 4.4 3.8 4 2.4 2.2 8 8 2 -999 -999 -999 7 2 12 18 2 4 3 10.8 4 3.6 3.7 2.6 2.3 8 8 1 -999 -999 -999 7 2 12 18 2 4 3 10 4.1 3.8 3.6 2.7 2 8 8 1 -999 -999 -999 7 2 12 18 2 4 3 10.2 4 3.5 4 2.4 2.2 8 8 1 -999 -999 -999 7 2 12 18 2 4 3 10 3.7 3.5 3.6 2.4 2.1 8 8 1 -999 -999 -999 7 2 12 18 2 4 3 10.3 4.2 3.7 3.7 3.2 2.5 6 8 1 -999 -999 -999 7 2 12 18 2 4 3 10.5 4 3.9 3.5 2.5 2.3 8 8 1 -999 -999 -999 7 2 12 18 2 4 3 9.2 4 3.5 3.6 2.3 2.4 8 8 1 -999 -999 -999 7 2 12 18 2 4 3 9.8 4 3.8 3.9 2.4 2.5 8 8 1 -999 -999 -999 7 2 12 18 2 4 3 11.1 4.5 3.7 4 2.8 2.2 8 8 1 -999 -999 -999 7 2 12 18 2 4 3 11 4.4 4 4.2 2.5 2.5 8 8 1 -999 -999 -999 7 2 12 18 2 4 3 11.3 4.2 4 4.2 2.8 2.5 8 8 1 -999 -999 -999 7 2 12 18 2 4 3 10.5 4 3.8 4 3 2 8 8 1 -999 -999 -999 7 2 12 18 2 4 3 10.8 4.2 3.7 4 2.5 2.2 8 8 1 -999 -999 -999 7 2 12 18 2 4 3 11 4.4 4 4.2 2.8 2.3 8 8 1 -999 -999 -999 7 2 12 18 2 4 3 9.8 3.8 3.6 3.4 2.4 2.4 8 8 1 -999 -999 -999 7 2 12 18 2 4 3 10.5 4.5 3.4 4.1 3 2.3 8 8 1 -999 -999 -999 7 2 12 18 2 4 3 10.2 4.2 3.8 3.6 2.8 2.6 8 8 1 -999 -999 -999 7 2 12 18 2 4 3 10 4 3.8 3.8 2.5 2 8 8 1 -999 -999 -999 7 2 12 18 2 4 3 10.7 4.2 4.1 4 4.5 2.2 8 8 1 -999 -999 -999 7 2 12 18 2 4 3 9.2 3.4 3.5 3.5 2 2 7 7 1 -999 -999 -999 7 2 12 18 2 4 3 10.7 4.4 3.7 4 2.8 2.3 8 8 1 -999 -999 -999 7 2 12 18 2 4 3 11.3 4 3.8 4 2.5 2.2 8 8 1 -999 -999 -999 7 2 12 18 2 4 3 9.5 4 3.5 3.8 2.5 2.3 8 8 1 -999 -999 -999 7 2 12 18 2 4 3 10.4 4.2 3.8 4 2.5 2.2 7 7 1 -999 -999 -999 7 2 12 18 2 4 3 10 4 3.5 3.6 2.3 2 8 8 1 -999 -999 -999 7 2 12 18 2 4 3 10.2 4.1 3.8 4 2.3 2.3 8 8 1 -999 -999 -999 7 2 12 18 2 4 3 10.6 5 4 4.3 2.4 2.3 8 8 1 -999 -999 -999 7 2 12 18 2 4 3 10.5 4.2 4 4 2.8 2.1 8 8 2 -999 -999 -999 7 2 12 18 2 4 3 9.5 4 3.5 3.8 3.8 2 8 7 2 -999 -999 -999 7 2 12 18 2 4 3 9.6 4 3.5 3.5 2.4 2 8 8 2 -999 -999 -999 7 2 12 18 2 4 3 9 4 3.5 3.5 2.5 2 8 8 2 -999 -999 -999 7 2 12 18 2 4 3 9 4 3.5 3.5 2.3 2.3 8 8 2 -999 -999 -999 7 2 12 18 2 4 3 10.3 3.8 3.6 4 2.8 2.1 8 8 2 -999 -999 -999 7 2 12 18 2 4 3 10 4 3.7 3.7 2.8 2.1 8 8 2 -999 -999 -999 7 2 12 18 2 4 3 9.7 4 3.5 3.7 2.8 2.2 8 8 2 -999 -999 -999 7 2 12 18 2 4 3 10.1 4 3.9 4 2 2.2 8 8 2 -999 -999 -999 Electronic Supplements to: Sukhodolskaya and Saveliev, Periodicum Biologorum, 2016, 118(3):273-280 DOI: 10.18054/pb.2016.118.3.3918 7 2 12 18 2 4 3 9.6 4 3.5 3.8 2.5 2 8 8 2 -999 -999 -999 7 2 12 18 2 4 3 9.5 4 3.6 3.3 2.5 2 8 8 2 -999 -999 -999 7 2 12 18 2 4 3 9.8 4.4 3.8 4 2.4 2.2 8 8 2 -999 -999 -999 7 2 19 5 4 2 10.5 7.7 4 4 2.9 3.5 7 7 1 -999 -999 -999 7 2 19 5 4 2 11 7.5 3.9 4.2 2.8 3 7 7 1 -999 -999 -999 7 2 19 5 4 2 8 7.9 3.1 3.2 1.9 1.9 7 7 1 -999 -999 -999 7 2 19 5 4 2 10.9 7.5 4 3.4 2.3 2.5 9 9 1 -999 -999 -999 7 2 19 5 4 2 10.4 7.6 4 4 2.5 2.5 8 8 1 -999 -999 -999 7 2 19 5 4 2 10.5 8.2 3.7 4 2 2.4 8 8 1 -999 -999 -999 7 2 19 5 4 2 11 7.6 3.2 4 2 2.3 9 9 1 -999 -999 -999 7 2 19 5 4 2 11.7 7.9 3.5 4.3 2 2.2 8 8 1 -999 -999 -999 7 2 19 5 4 2 10.8 7.5 3.7 4 2.1 2.3 8 8 1 -999 -999 -999 7 2 19 5 4 2 11.2 7.2 3.8 4 2.1 2.4 9 9 1 -999 -999 -999 7 2 19 5 4 2 10.5 7.9 3.7 4.7 2 2.2 9 9 1 -999 -999 -999 7 2 19 5 4 2 9.5 7.9 3.5 3.5 2 2.2 8 8 1 -999 -999 -999 7 2 19 5 4 2 11.5 7.5 4 4.1 2.2 2.4 9 9 1 -999 -999 -999 7 2 19 5 4 2 10.5 7.8 3.6 4 2 2 8 8 1 -999 -999 -999 7 2 19 5 4 2 10.8 8.2 3.9 4 2.6 2.2 9 9 1 -999 -999 -999 7 2 19 5 4 2 10.7 8.4 3.8 4 2 2.3 9 9 1 -999 -999 -999 7 2 19 5 4 2 10 8.2 3.6 4 2.1 2.2 7 7 2 -999 -999 -999 7 2 19 5 4 2 9.5 7.8 3.6 3.5 2 2.2 9 9 2 -999 -999 -999 7 2 19 5 4 2 10.2 7.9 3.5 3.5 2 2 9 9 2 -999 -999 -999 7 2 19 5 4 2 10 8.4 3.5 3.7 1.5 2.2 8 8 2 -999 -999 -999 7 2 19 5 4 2 10.5 7.4 3.5 4 2.2 2.2 9 9 2 -999 -999 -999 7 2 19 5 4 2 10.5 7.9 4 4 2.9 3.5 7 7 1 -999 -999 -999 7 2 19 5 4 2 11 8 3.9 4.2 2.8 3 7 7 1 -999 -999 -999 7 2 19 5 4 2 8 7.8 3.1 3.2 1.9 1.9 7 7 1 -999 -999 -999 7 2 19 5 4 2 10.9 8.3 4 3.4 2.3 2.5 9 9 1 -999 -999 -999 7 2 19 5 4 2 10.4 6.9 4 4 2.5 2.5 8 8 1 -999 -999 -999 7 2 19 5 4 2 10.5 8.1 3.7 4 2 2.4 8 8 1 -999 -999 -999 7 2 19 5 4 2 11 7.8 3.2 4 2 2.3 9 9 1 -999 -999 -999 7 2 19 5 4 2 11.7 7.5 3.5 4.3 2 2.2 8 8 1 -999 -999 -999 7 2 19 5 4 2 10.8 8 3.7 4 2.1 2.3 8 8 1 -999 -999 -999 7 2 19 5 4 2 11.2 7.5 3.8 4 2.1 2.4 9 9 1 -999 -999 -999 7 2 19 5 4 2 10.5 7.9 3.7 4.7 2 2.2 9 9 1 -999 -999 -999 7 2 19 5 4 2 9.5 9 3.5 3.5 2 2.2 8 8 1 -999 -999 -999 7 2 19 5 4 2 11.5 8.2 4 4.1 2.2 2.4 9 9 1 -999 -999 -999 7 2 19 5 4 2 10.5 7.5 3.6 4 2 2 8 8 1 -999 -999 -999 7 2 19 5 4 2 10.8 7.5 3.9 4 2.6 2.2 9 9 1 -999 -999 -999 7 2 19 5 4 2 10.7 7.5 3.8 4 2 2.3 9 9 1 -999 -999 -999 7 2 19 5 4 2 10 7.5 3.6 4 2.1 2.2 7 7 2 -999 -999 -999 7 2 19 5 4 2 9.5 7.4 3.6 3.5 2 2.2 9 9 2 -999 -999 -999 7 2 19 5 4 2 10.2 7.7 3.5 3.5 2 2 9 9 2 -999 -999 -999 7 2 19 5 4 2 10 7.5 3.5 3.7 1.5 2.2 8 8 2 -999 -999 -999 7 2 19 5 4 2 10.5 7.9 3.5 4 2.2 2.2 9 9 2 -999 -999 -999 7 3 11 22 1 1 4 11.5 5.2 4 4 2.8 2.3 8 9 1 -999 -999 -999 7 3 11 22 1 1 4 8.5 4.4 3.3 3.4 2.1 2.3 9 9 1 -999 -999 -999 7 3 11 22 1 1 4 11.3 5 4 4 2.9 2.4 9 9 1 -999 -999 -999 7 3 11 22 1 1 4 11 4.9 3.4 3.5 2.4 2.4 9 10 1 -999 -999 -999 7 3 11 22 1 1 4 10.7 5.1 4 3.7 2.4 2.5 9 10 1 -999 -999 -999 7 3 11 22 1 1 4 11.2 5.1 4 3.8 2.2 2.2 9 8 1 -999 -999 -999 7 3 11 22 1 1 4 11.5 5.5 4.1 3.8 2.8 2.5 9 9 1 -999 -999 -999 7 3 11 22 1 1 4 10.1 4.6 3.6 3.5 2.4 2.2 9 9 1 -999 -999 -999 7 3 11 22 1 1 4 11 5.1 4 3.6 2.5 2.3 9 9 1 -999 -999 -999 7 3 11 22 1 1 4 11 5.5 4 4 2.5 2.5 9 9 1 -999 -999 -999 7 3 11 22 1 1 4 10.8 5 3.7 3.8 2.6 2.4 9 9 1 -999 -999 -999 7 3 11 22 1 1 4 10 4.8 3.5 3.4 2.7 2.2 9 10 1 -999 -999 -999 7 3 11 22 1 1 4 11 5 4.1 3.8 2.4 2.4 9 10 2 -999 -999 -999 7 3 11 22 1 1 4 10.2 5 3.9 3.5 2.5 2.3 9 9 2 -999 -999 -999 Electronic Supplements to: Sukhodolskaya and Saveliev, Periodicum Biologorum, 2016, 118(3):273-280 DOI: 10.18054/pb.2016.118.3.3918 7 3 11 22 1 1 4 10.1 4.9 3.7 3.8 2.2 2.2 9 8 2 -999 -999 -999 7 3 11 22 1 1 4 10 4.6 3.8 3.7 2.3 2.3 9 9 2 -999 -999 -999 7 3 11 22 1 1 4 9.8 4.6 3.5 3.5 2.4 2.4 9 9 2 -999 -999 -999 7 3 11 22 1 1 4 9.9 4.8 3.4 3.5 2.2 2.4 9 8 2 -999 -999 -999 7 3 11 22 1 1 4 10 5 3.7 3.5 2.2 2.1 9 8 2 -999 -999 -999 7 3 11 22 1 1 4 10.7 4.9 3.7 3.2 2.4 2 9 9 2 -999 -999 -999 7 3 11 22 1 1 4 10.2 4.4 3.5 3 2.5 2.2 10 10 2 -999 -999 -999 7 3 11 22 1 1 4 11 3.9 3.4 3.2 2.3 2.2 9 9 2 -999 -999 -999 7 3 11 23 1 1 4 11.3 5.2 4.2 3.7 2.5 2.4 8 9 1 -999 -999 -999 7 3 11 23 1 1 4 10.4 5.1 3.9 3.5 2.5 2.3 9 9 1 -999 -999 -999 7 3 11 23 1 1 4 8.7 5 3.4 3.4 2.3 2.3 9 9 1 -999 -999 -999 7 3 11 23 1 1 4 10.7 5.3 4 3.6 2.5 2.3 9 9 1 -999 -999 -999 7 3 11 23 1 1 4 9.7 5 3.5 3.5 2.4 2.2 9 10 1 -999 -999 -999 7 3 11 23 1 1 4 10.5 5 4 3.8 2.4 2.4 8 10 1 -999 -999 -999 7 3 11 23 1 1 4 10.9 5.8 4 3.5 2.4 2.3 8 9 1 -999 -999 -999 7 3 11 23 1 1 4 11.4 5 4 4.3 2.5 2.4 9 8 1 -999 -999 -999 7 3 11 23 1 1 4 10 4.9 3.7 3.5 2 2.1 9 8 1 -999 -999 -999 7 3 11 23 1 1 4 10.1 5 3.8 3.9 2.3 2.4 9 9 1 -999 -999 -999 7 3 11 23 1 1 4 10 4.8 3.8 3.8 2.3 2.4 9 9 1 -999 -999 -999 7 3 11 23 1 1 4 9.7 5 4 4.2 2.2 2 9 8 1 -999 -999 -999 7 3 11 23 1 1 4 9 5 4 4.3 2.2 2.1 10 11 1 -999 -999 -999 7 3 11 23 1 1 4 10.2 4.5 3.5 4 2.1 2.3 10 10 1 -999 -999 -999 7 3 11 23 1 1 4 11 4.4 4 4.1 2.1 2.1 8 8 1 -999 -999 -999 7 3 11 23 1 1 4 11 4.9 3.4 3.5 2.4 2.4 9 10 1 -999 -999 -999 7 3 11 23 1 1 4 10.7 5.1 4 3.7 2.4 2.5 9 10 1 -999 -999 -999 7 3 11 23 1 1 4 11 5.5 4 4 2.5 2.5 9 9 1 -999 -999 -999 7 3 11 23 1 1 4 8.9 4.4 3.3 3.4 2.3 2.1 9 8 1 -999 -999 -999 7 3 11 23 1 1 4 11 5 4 3.6 2.5 2.3 9 9 1 -999 -999 -999 7 3 11 23 1 1 4 11.5 5.2 4 4 2.8 2.3 8 9 1 -999 -999 -999 7 3 11 23 1 1 4 11.2 4.8 3.9 4 2.9 2.2 10 10 1 -999 -999 -999 7 3 11 23 1 1 4 10.9 4.4 3.8 4 2.7 2.2 8 8 1 -999 -999 -999 7 3 11 23 1 1 4 11.2 4 3.8 3.8 2.5 2.1 9 10 1 -999 -999 -999 7 3 11 23 1 1 4 10.7 5.9 3.3 3.5 2.2 1.9 8 8 1 -999 -999 -999 7 3 11 23 1 1 4 10 5 3.7 3.8 2.4 2.2 9 9 2 -999 -999 -999 7 3 11 23 1 1 4 9.7 4.9 3.9 4 2.2 2 10 9 2 -999 -999 -999 7 3 11 23 1 1 4 10.2 4 3.9 3 2 2 8 8 2 -999 -999 -999 7 3 11 23 1 1 4 10 4.9 3.7 3.5 2.4 2.2 8 8 2 -999 -999 -999 7 3 11 23 1 1 4 10.5 5 3.5 3.4 2.4 2.3 9 9 2 -999 -999 -999 7 3 11 23 1 1 4 10 4.9 3.7 3.5 2 2.1 8 8 2 -999 -999 -999 7 3 11 23 1 1 4 9 4.8 3.8 3.5 2.1 2 9 8 2 -999 -999 -999 7 3 11 23 1 1 4 10.7 4.9 3.7 3.2 2.4 2 9 9 2 -999 -999 -999 7 3 11 23 1 1 4 10.8 4.5 3.5 4 2.2 2.1 10 10 2 -999 -999 -999 7 3 11 23 1 1 4 11 4.2 3.8 4 2.2 2 11 11 2 -999 -999 -999 7 3 11 23 1 1 4 9.9 4 3.8 3.9 2.5 2 11 11 2 -999 -999 -999 7 3 11 23 1 1 4 10 4 4 3.8 2.6 1.8 13 11 2 -999 -999 -999 7 3 11 23 1 1 4 9.9 4.8 3.4 3.5 2.2 2.4 9 8 2 -999 -999 -999 7 3 11 23 1 1 4 10.2 4.6 3.8 3.7 2.3 2.3 8 10 2 -999 -999 -999 7 3 11 23 1 1 4 10.1 4.9 3.7 3.9 2.2 2.2 9 9 2 -999 -999 -999 7 3 11 23 1 1 4 11.1 4.4 3.9 4.2 2.5 2.2 9 9 2 -999 -999 -999 7 3 11 23 1 1 4 10.7 5 4 4.1 2.4 2 8 8 2 -999 -999 -999 7 3 11 26 1 1 4 10.4 4.9 3.7 4 2.4 2.3 9 9 1 -999 -999 -999 7 3 11 26 1 1 4 10 5 3.5 4 1.8 2.2 8 8 1 -999 -999 -999 7 3 11 26 1 1 4 10.8 5.2 3.8 3.7 2.5 2.5 8 8 1 -999 -999 -999 7 3 11 26 1 1 4 10.8 5 4 3.6 2.2 2.2 8 8 1 -999 -999 -999 7 3 11 26 1 1 4 10.4 5 3.4 3.5 2 2.1 9 9 1 -999 -999 -999 7 3 11 26 1 1 4 9.2 5 3.3 3.5 2 2.4 9 9 1 -999 -999 -999 7 3 11 26 1 1 4 9.5 4.9 3.5 3.6 2.5 2.3 9 9 1 -999 -999 -999 7 3 11 26 1 1 4 11 5 4.2 4 2.4 2.4 8 8 1 -999 -999 -999 7 3 11 26 1 1 4 9.5 4.2 3.5 3.5 1.9 2.1 9 9 1 -999 -999 -999 Electronic Supplements to: Sukhodolskaya and Saveliev, Periodicum Biologorum, 2016, 118(3):273-280 DOI: 10.18054/pb.2016.118.3.3918 7 3 11 26 1 1 4 9.9 4.8 3.5 3.4 2.1 2.3 9 9 2 -999 -999 -999 7 3 11 26 1 1 4 8.3 5 3.4 4 2.5 2.4 9 10 2 -999 -999 -999 7 3 11 26 1 1 4 10.4 5 3.9 4 2.2 2.4 9 9 2 -999 -999 -999 7 3 11 26 1 1 4 10.5 5.1 3.8 3.7 2.3 2 9 9 1 -999 -999 -999 7 3 11 27 19 1 4 11 5.1 4.4 4 2.5 2.5 8 9 1 -999 -999 -999 7 3 11 27 19 1 4 9.3 4.4 3.8 3.3 2 2.1 9 8 1 -999 -999 -999 7 3 11 27 19 1 4 12.2 5 4.1 4.2 2.6 2.4 9 9 1 -999 -999 -999 7 3 11 27 19 1 4 11 5 3.7 3.7 2.3 2.2 9 9 1 -999 -999 -999 7 3 11 27 19 1 4 11 4.9 4 4 2.4 2.4 8 10 1 -999 -999 -999 7 3 11 27 19 1 4 10 4.6 3.7 3.6 2.3 2.1 9 9 2 -999 -999 -999 7 3 11 27 19 1 4 10 4.8 3.5 3.5 2.4 2.1 9 9 2 -999 -999 -999 7 3 11 28 1 2 3 11 5.1 4 4 2.5 2.3 9 9 1 -999 -999 -999 7 3 11 28 1 2 3 10 5 3.5 3.8 2.3 2.3 9 10 1 -999 -999 -999 7 3 11 28 1 2 3 10.5 5.2 3.5 3.7 2.1 2.2 9 9 1 -999 -999 -999 7 3 11 28 1 2 3 10.5 5 3.5 3.5 2.2 2.2 9 8 1 -999 -999 -999 7 3 11 28 1 2 3 10.7 5 3.7 3.5 1.9 2.1 9 9 1 -999 -999 -999 7 3 11 28 1 2 3 11.2 5 3.8 3.7 2 2 8 8 1 -999 -999 -999 7 3 11 28 1 2 3 11 4.7 3.5 3.5 2.2 2.2 10 10 1 -999 -999 -999 7 3 11 28 1 2 3 10 5.2 3.6 4 2.2 2.4 8 8 1 -999 -999 -999 7 3 11 28 1 2 3 11 5 4 3.7 2.4 2.5 8 8 1 -999 -999 -999 7 3 11 28 1 2 3 9 4.8 3.4 3.9 2.3 2.3 8 8 1 -999 -999 -999 7 3 11 28 1 2 3 11 5 3.8 3.7 2.1 2.3 9 9 1 -999 -999 -999 7 3 11 28 1 2 3 10.4 4.9 3.5 3.9 1.9 2.2 8 9 1 -999 -999 -999 7 3 11 28 1 2 3 10.9 5 4 3.6 2 2.3 9 9 1 -999 -999 -999 7 3 11 28 1 2 3 11.2 4.7 3.8 4 2 2 10 9 1 -999 -999 -999 7 3 11 28 1 2 3 10.5 5 4 3.7 2 2.3 8 8 1 -999 -999 -999 7 3 11 28 1 2 3 10 4.9 3.5 3.6 2.2 2.2 8 9 1 -999 -999 -999 7 3 11 28 1 2 3 10.2 5 3.8 4 2.5 2.2 9 9 1 -999 -999 -999 7 3 11 28 1 2 3 10.9 5.1 4 3.9 2.3 2 9 9 1 -999 -999 -999 7 3 11 28 1 2 3 11 5 4 3.8 2.2 2 9 9 1 -999 -999 -999 7 3 11 28 1 2 3 11.2 4.9 3.8 3.7 2.1 2 10 10 1 -999 -999 -999 7 3 11 28 1 2 3 10.5 4.8 3.8 3.5 1.8 2.3 8 10 1 -999 -999 -999 7 3 11 28 1 2 3 10.7 4.4 3.8 3.5 2.3 2 9 9 1 -999 -999 -999 7 3 11 28 1 2 3 10 5 3.7 3.5 2.2 2.2 9 8 2 -999 -999 -999 7 3 11 28 1 2 3 8.7 4.5 3.5 3.4 1.7 2.2 10 9 2 -999 -999 -999 7 3 11 28 1 2 3 10.2 5 3.8 3.5 2 2.2 8 8 2 -999 -999 -999 7 3 11 28 1 2 3 9.9 4.8 3.8 3.4 2.5 2 8 8 2 -999 -999 -999 7 3 11 28 1 2 3 9.9 5 3.6 3.6 2.2 2.2 9 8 2 -999 -999 -999 7 3 11 28 1 2 3 9 4.4 3.5 3.5 2 2 9 8 2 -999 -999 -999 7 3 11 28 1 2 3 10 4.9 3.7 3.7 2.4 2.1 9 9 2 -999 -999 -999 7 3 11 28 1 2 3 9.2 4.2 3.4 3.3 1.9 2.3 9 9 2 -999 -999 -999 7 3 11 28 1 2 3 9.5 4.8 3.6 3.5 1.8 1.8 8 8 2 -999 -999 -999 7 3 11 28 1 2 3 9.3 4.8 3.5 3.4 2 2 9 9 2 -999 -999 -999 7 3 11 28 1 2 3 10 4.7 3.5 3.5 1.9 2.1 10 9 2 -999 -999 -999 7 3 11 28 1 2 3 10 4.8 3.5 4 2.1 2.3 9 9 2 -999 -999 -999 7 3 11 28 1 2 3 10.2 5 3.6 3.8 2.3 2.1 9 9 2 -999 -999 -999 7 3 11 28 1 2 3 9.8 5 3.4 3.5 2 2 9 9 2 -999 -999 -999 7 3 11 28 1 2 3 10 4.5 3.5 3.7 2 2.2 10 10 2 -999 -999 -999 7 3 11 28 1 2 3 9.7 4.4 3.7 4 2 2 10 9 2 -999 -999 -999 7 3 11 28 1 2 3 9.5 5 3.5 3.7 2.2 2 8 8 2 -999 -999 -999 7 3 11 28 1 2 3 10.1 4.8 3.3 3.5 1.9 1.8 8 8 2 -999 -999 -999 7 3 11 25 1 1 4 11.5 5.4 4 4 2.6 2.4 9 9 1 -999 -999 -999 7 3 11 25 1 1 4 10.4 5.2 3.7 4 2.6 2.5 8 8 1 -999 -999 -999 7 3 11 25 1 1 4 10.7 4.9 3.8 3.8 2.2 2.4 9 9 1 -999 -999 -999 7 3 11 25 1 1 4 10.2 4.9 3.7 3.5 2 2 9 9 1 -999 -999 -999 7 3 11 25 1 1 4 10.6 5 3.8 4 2.4 2.3 8 9 1 -999 -999 -999 7 3 11 25 1 1 4 10.9 5 3.8 3.8 2.2 2.2 9 9 1 -999 -999 -999 7 3 11 25 1 1 4 11.3 4.7 3.8 3.9 2.3 2 8 8 1 -999 -999 -999 7 3 11 25 1 1 4 11 4.8 4 3.7 2 2.3 8 8 1 -999 -999 -999 Electronic Supplements to: Sukhodolskaya and Saveliev, Periodicum Biologorum, 2016, 118(3):273-280 DOI: 10.18054/pb.2016.118.3.3918 7 3 11 25 1 1 4 10.5 5 3.5 3.7 2.2 2.4 8 9 1 -999 -999 -999 7 3 11 25 1 1 4 9.6 5 3.8 3.5 2.1 2.1 9 9 1 -999 -999 -999 7 3 11 25 1 1 4 10.6 5.2 4 3.9 2.5 2.2 9 9 1 -999 -999 -999 7 3 11 25 1 1 4 10.3 4.9 3.9 3.5 2.4 2.5 9 9 1 -999 -999 -999 7 3 11 25 1 1 4 9.4 4.4 3.5 3.5 1.9 2.3 8 8 1 -999 -999 -999 7 3 11 25 1 1 4 11 5 3.8 3.5 2.4 2.2 10 9 1 -999 -999 -999 7 3 11 25 1 1 4 10.7 5 3.8 3.7 2.2 2 8 8 1 -999 -999 -999 7 3 11 25 1 1 4 10.5 5 3.5 3.5 2 2.2 8 8 1 -999 -999 -999 7 3 11 25 1 1 4 10.7 5.2 4 4 2.5 2.4 9 9 1 -999 -999 -999 7 3 11 25 1 1 4 9.7 4.5 3.6 3.7 1.9 2 8 9 1 -999 -999 -999 7 3 11 25 1 1 4 10 5 3.5 3.8 2 2.3 9 9 1 -999 -999 -999 7 3 11 25 1 1 4 10.2 5 3.7 4 2 2 10 10 1 -999 -999 -999 7 3 11 25 1 1 4 10.5 4.9 3.8 3.5 2.1 2.2 9 9 1 -999 -999 -999 7 3 11 25 1 1 4 10.7 5.1 4 3.9 2.1 2.2 8 9 2 -999 -999 -999 7 3 11 25 1 1 4 9.8 4.8 3.5 3.6 2.3 2.2 9 9 2 -999 -999 -999 7 3 11 25 1 1 4 9.2 4.8 3.4 3.5 2 2 8 9 2 -999 -999 -999 7 3 11 25 1 1 4 10.3 5 4 3.7 2.3 2.3 8 8 2 -999 -999 -999 7 3 11 25 1 1 4 8.5 4 3.1 3.4 1.9 2.4 8 8 2 -999 -999 -999 7 3 11 25 1 1 4 9 4.4 3.5 3.5 2 2 9 9 2 -999 -999 -999 7 3 11 25 1 1 4 9.4 5 3.3 3.7 2 2.2 10 8 2 -999 -999 -999 7 3 11 25 1 1 4 9.7 4.6 3.5 3.5 2.2 1.9 9 9 2 -999 -999 -999 7 3 11 25 1 1 4 11 5 4 4 2 2.2 8 8 2 -999 -999 -999 7 3 11 25 1 1 4 9 4.8 3.5 3.9 1.9 2 8 8 2 -999 -999 -999 7 3 11 25 1 1 4 8.7 4 3.2 3 1.8 1.9 8 9 2 -999 -999 -999 7 3 11 25 1 1 4 9.7 4.9 3.7 3.5 2.2 2 8 9 2 -999 -999 -999 7 3 11 25 1 1 4 10 4.9 3.7 3.6 2.3 2.2 9 8 2 -999 -999 -999 7 3 11 25 1 1 4 9.9 5 3.5 3.3 2 2 9 9 2 -999 -999 -999 7 3 11 25 1 1 4 9.5 4.4 3.7 3.5 2.2 2 9 9 2 -999 -999 -999 7 3 11 25 1 1 4 9.7 4.2 3.5 3.5 1.9 2.1 8 8 2 -999 -999 -999 7 3 11 25 1 1 4 9.7 4.4 3.5 3.3 1.9 2 8 8 2 -999 -999 -999 7 3 11 25 1 1 4 10 4.5 3.5 3 2.3 2.2 8 8 2 -999 -999 -999 7 3 11 25 1 1 4 9.5 4.2 3.4 3.4 1.8 2 8 9 2 -999 -999 -999 7 3 11 25 1 1 4 9.3 3.8 3.3 3 2.1 1.9 8 8 2 -999 -999 -999 7 3 11 29 1 4 3 10.5 5.1 4 4 2.5 2.4 9 9 1 -999 -999 -999 7 3 11 29 1 4 3 10 5 4 3.5 2 2.1 9 9 1 -999 -999 -999 7 3 11 29 1 4 3 11 5 4 4 2.2 2.5 9 8 1 -999 -999 -999 7 3 11 29 1 4 3 11.2 4.8 3.5 3.7 2 2.2 8 8 1 -999 -999 -999 7 3 11 29 1 4 3 10.8 4.7 3.7 3.5 2.1 2 9 9 1 -999 -999 -999 7 3 11 29 1 4 3 10.7 5 4 3.5 2 2.3 8 9 1 -999 -999 -999 7 3 11 29 1 4 3 10.5 4.8 3.8 3.5 2 2 10 10 1 -999 -999 -999 7 3 11 29 1 4 3 10.2 4.7 4 3.7 2.2 2.3 9 9 1 -999 -999 -999 7 3 11 29 1 4 3 10 4.4 3.8 3.5 2.4 2.2 8 8 2 -999 -999 -999 7 3 11 29 1 4 3 9.3 4.2 3.5 3.4 2.1 1.9 9 9 2 -999 -999 -999 7 3 11 29 1 4 3 10.7 4.6 4 4 1.9 2.2 9 8 2 -999 -999 -999 7 3 11 29 1 4 3 9.5 5 3.4 3.5 1.8 2.1 10 10 2 -999 -999 -999 7 3 11 29 1 4 3 10 4.9 4 3.6 2.2 1.9 9 9 2 -999 -999 -999 7 3 11 29 1 4 3 9.7 5 3.7 3.7 2 2 8 9 2 -999 -999 -999 7 3 11 29 1 4 3 10 4.5 3.5 3.5 2 2 9 9 2 -999 -999 -999 7 3 11 29 1 4 3 10.3 4.6 3.5 3.8 2.1 1.9 9 9 2 -999 -999 -999 7 3 11 29 1 4 3 9.5 4.5 3.7 3.5 2.2 1.9 9 9 2 -999 -999 -999 7 3 11 29 1 4 3 10 4.6 3.9 4 2 2 8 9 2 -999 -999 -999 7 7 -999 -999 20 4 3 9 2.6 3 3 2 2 8 7 1 -999 -999 -999 7 7 -999 -999 20 4 3 9 2.5 3.2 3 1.7 2 8 8 1 -999 -999 -999 7 7 -999 -999 20 4 3 9 2.2 3.4 3.5 2 2.4 8 8 1 -999 -999 -999 7 7 -999 -999 20 4 3 9.7 2.9 3.8 4.1 3 2.3 9 9 1 -999 -999 -999 7 7 -999 -999 20 4 3 10.8 3 4 4.3 2.5 2.5 10 10 1 -999 -999 -999 7 7 -999 -999 20 4 3 10.7 3 4.1 4.6 2.6 2.6 10 10 1 -999 -999 -999 7 7 -999 -999 20 4 3 9 2.3 3.3 3.5 2.5 2.2 9 9 2 -999 -999 -999 7 7 -999 -999 20 4 3 8.5 2.4 3.2 3.2 3 2.2 9 9 2 -999 -999 -999 Electronic Supplements to: Sukhodolskaya and Saveliev, Periodicum Biologorum, 2016, 118(3):273-280 DOI: 10.18054/pb.2016.118.3.3918 7 7 -999 -999 20 4 3 8.5 2.5 3.5 3.2 2.3 2 10 9 2 -999 -999 -999 7 7 -999 -999 20 4 3 11.6 3.1 4.3 4.5 2.8 2.5 10 10 2 -999 -999 -999 7 7 -999 -999 20 4 3 10.5 2.7 4 4.1 2.5 2.4 9 8 2 -999 -999 -999 7 7 -999 -999 20 4 3 10 2.9 3.5 4 2.3 2.3 10 10 2 -999 -999 -999 7 7 -999 -999 20 4 3 10 2.7 3.7 4 2.4 2.4 10 10 2 -999 -999 -999 7 7 -999 -999 20 4 3 9.6 2.6 3.7 3.8 2.5 2.3 10 10 2 -999 -999 -999 7 7 -999 -999 20 4 3 10.1 2.8 3.8 3.9 2.5 2.3 10 10 2 -999 -999 -999 7 7 -999 -999 20 4 3 9.7 2.6 3.6 3.8 2.5 2.3 9 9 2 -999 -999 -999 7 7 -999 -999 20 4 3 10.5 2.8 3.7 4.4 2 2.3 9 10 2 -999 -999 -999 7 7 -999 -999 20 4 3 10.2 2.8 4 4 2 2.3 9 9 2 -999 -999 -999 7 6 -999 -999 6 4 3 9.7 2.6 3.8 4.2 2.7 2.3 10 10 1 -999 -999 -999 7 6 -999 -999 6 4 3 10 3 4 4.2 2.5 2.3 10 10 1 -999 -999 -999 7 6 -999 -999 6 4 3 10.5 3 4 4.2 2.5 2.3 10 10 1 -999 -999 -999 7 6 -999 -999 6 4 3 10.8 2.9 4 4.2 2.8 2.4 10 10 1 -999 -999 -999 7 6 -999 -999 6 4 3 10.5 3 4 4.5 2.5 2.3 10 10 1 -999 -999 -999 7 6 -999 -999 6 4 3 10.3 2.8 3.7 4 2.5 2.3 10 10 2 -999 -999 -999 7 6 -999 -999 6 4 3 10 2.8 3.5 4.3 2.4 2.5 10 10 2 -999 -999 -999 7 6 -999 -999 6 4 3 10.1 2.5 3.9 4.2 2.9 2.3 10 10 2 -999 -999 -999 7 6 -999 -999 6 4 3 10.5 2.6 4.2 4.5 3.1 2.5 10 10 2 -999 -999 -999 7 5 -999 -999 1 4 3 10.2 3 3.8 4.5 2.5 2.3 10 10 1 -999 -999 -999 7 5 -999 -999 1 4 3 10 3.2 3.8 4 2.5 2.4 10 10 1 -999 -999 -999 7 5 -999 -999 1 4 3 10 2.4 3.7 4.1 2.5 2.3 10 10 1 -999 -999 -999 7 5 -999 -999 1 4 3 10.5 2.8 4 4.1 2.5 2.2 10 10 1 -999 -999 -999 7 5 -999 -999 1 4 3 11.2 3 4 4.5 2.8 2.2 10 10 1 -999 -999 -999 7 5 -999 -999 1 4 3 10.2 2.8 3.9 4.4 2.7 2.3 10 10 1 -999 -999 -999 7 5 -999 -999 1 4 3 11 2.9 4 4.4 3 2.3 10 10 1 -999 -999 -999 7 5 -999 -999 1 4 3 11 3 4 4.3 3 2.3 10 10 1 -999 -999 -999 7 5 -999 -999 1 4 3 11 3 4 4.5 3 2.5 10 10 1 -999 -999 -999 7 5 -999 -999 1 4 3 10.5 2.7 3.8 4.3 2.8 2.4 10 10 1 -999 -999 -999 7 5 -999 -999 1 4 3 10.7 2.8 4 4.4 3 2.5 10 10 1 -999 -999 -999 7 5 -999 -999 1 4 3 10.8 2.7 4 4.3 3 2.4 10 10 1 -999 -999 -999 7 5 -999 -999 1 4 3 10.1 2.8 3.8 4.5 3 2.2 10 10 2 -999 -999 -999 7 5 -999 -999 1 4 3 10 2.6 3.8 4 2.5 2.2 10 10 -999 -999 -999 -999 Electronic Supplements to: Sukhodolskaya and Saveliev, Periodicum Biologorum, 2016, 118(3):273-280 DOI: 10.18054/pb.2016.118.3.3918 S3 Denotations for columns in S2 (Data set for P. niger) 1. A – species 2. B – region 1. Tatarstan 2. Sverdlovsk region 3. Kemerovo region 4. Novosibirsk region 5. Udmurtia 6. Mariy El 7. Cis_Ural 8. Stavropol 3. C – district 4. D – settlement 5. E – biotope type 1. meadow 2. birch 3. swamps 4. elm 5. oak 6. pine 7. lime 8. carr 9. shrubs 10. barley 11. maize 12. vetch&oat 13. pea 14. wheat 15. carrot 16. spring wheat 17. alfalfa 18. rye 19. lawn 20. spruce 6. F – degree of anthropogenic impact 1. urban 2. suburban 3. rural 4. natural 7. G – isolation 1. island 2. floodland 3. table‐land 4. urbancenosis 8. H – elytra length 9. I – elytra width 10. J – pronotum length 11. K – pronotum width 12. L – head length 13. M – distance between eyes 16. P – sex 1. female 2. male ‐0,999 – no data Electronic Supplements to: Sukhodolskaya and Saveliev, Periodicum Biologorum, 2016, 118(3):273-280 DOI: 10.18054/pb.2016.118.3.3918 S4 Results of modeling of different factors effect on traits variation in P. niger Call: lm(formula = Elytra.Length~ fSex/(fRegion +fAntrop +fHabitat), data = cur.data, weights = Wts, contrasts= list(fRegion = ct.Region, fAntrop= ct.Antrop, fHabitat= ct.Habitat)) Residuals: Min 1Q Median 3Q Max ‐2.59375 ‐0.337 45 0.09114 0.31719 2.51620 Coefficients: (4 not defined because of singularities) Estimate Std. Error t value Pr(>|t|) (Intercept) 11.159580 0.042215 264.353 < 2e‐16 *** fSex2 ‐0.620452 0.099986 ‐6.205 6.79e‐10 *** fSex1:fRegion2 ‐0.804024 0.091794 ‐8.759 < 2e‐16 *** fSex2:fRegion2 ‐0.822461 0.152199 ‐5.404 7.42e‐08 *** fSex1:fRegion3 ‐0.181747 0.165567 ‐1.098 0.272473 fSex2:fRegion3 ‐0.726118 0.258056 ‐2.814 0.004951 ** fSex1:fRegion5 ‐0.227226 0.317668 ‐0.715 0.474523 fSex2:fRegion5 ‐0.558479 0.587493 ‐0.951 0.341931 fSex1:fRegion6 ‐0.859580 0.271180 ‐3.170 0.001552 ** fSex2:fRegion6 ‐0.314127 0.312907 ‐1.004 0.315564 fSex1:fRegion7 ‐1.459580 0.248151 ‐5.882 4.85e‐09 *** fSex2:fRegion7 ‐0.689127 0.195227 ‐3.530 0.000426 *** fSex1:fAntrop1 ‐0.131618 0.223884 ‐0.588 0.556686 fSex2:fAntrop1 0.058000 0.207494 0.280 0.779874 fSex1:fAntrop2 ‐0.003409 0.247297 ‐0.014 0.989003 fSex2:fAntrop2 ‐0.177778 0.236242 ‐0.753 0.451838 fSex1:fHabitat1 ‐0.365332 0.272107 ‐1.343 0.179573 fSex2:fHabitat1 0.086991 0.332695 0.261 0.793758 fSex1:fHabitat4 ‐0.276175 0.053915 ‐5.122 3.35e‐07 *** fSex2:fHabitat4 ‐0.318162 0.111294 ‐2.859 0.004303 ** fSex1:fHabitat5 0.238194 0.133626 1.783 0.074834 . fSex2:fHabitat5 0.323333 0.225449 1.434 0.151701 fSex1:fHabitat6 NA NA NA NA fSex2:fHabitat6 NA NA NA NA fSex1:fHabitat7 ‐1.576647 0.257562 ‐6.121 1.14e‐09 *** fSex2:fHabitat7 ‐1.004367 0.253019 ‐3.970 7.49e‐05 *** fSex1:fHabitat1 9 0.053785 0.388683 0.138 0.889957 fSex2:fHabitat1 9 0.128991 0.545208 0.237 0.813002 fSex1:fHabitat2 0 NA NA NA NA fSex2:fHabitat2 0 NA NA NA NA ‐‐‐ Signif. codes: 0 ‘***’ 0. 001 ‘**’ 0. 01 ‘*’ 0 .05 ‘.’ 0 .1 ‘ ’ 1 Residual standard error: 0.599 on 1753 degrees of freedom Multiple R‐squared: 0.2791, AdjustedR‐squared: 0.2688 F‐statistic: 27.15 on 25 and 1753 DF,p‐value: < 2.2e‐16 Analysis of Variance Table Response: Elytra.Length Electronic Supplements to: Sukhodolskaya and Saveliev, Periodicum Biologorum, 2016, 118(3):273-280 DOI: 10.18054/pb.2016.118.3.3918 Df Sum Sq Mean Sq F v alue Pr(>F) fSex 1 114.94 114.939 320 .358 < 2 .2e‐16 ** * fSex:fRegion 10 42.90 4.290 11 .957 < 2 .2e‐16 ** * fSex:fAntrop 4 46.51 11.627 32 .407 < 2 .2e‐16 ** * fSex:fHabitat 10 39.17 3.917 10 .919 < 2 .2e‐16 ** * Residuals 1 753 628.94 0.359 ‐‐‐ Signif. codes: 0 ‘***’ 0. 001 ‘**’ 0. 01 ‘*’ 0 .05 ‘.’ 0 .1 ‘ ’ 1 Electronic Supplements to: Sukhodolskaya and Saveliev, Periodicum Biologorum, 2016, 118(3):273-280 DOI: 10.18054/pb.2016.118.3.3918 Call: lm(formula = Elytra.Width~ fSex/(fRegion + fAntrop +fHabitat), data = cur.data, weights = Wts, contrasts= list(fRegion = ct.Region, fAntrop= ct.Antrop, fHabitat= ct.Habitat)) Residuals: Min 1Q Median 3Q Max ‐1.44115 ‐0.116 42 0.00000 0.09885 1.19688 Coefficients: (4 not defined because of singularities) Estimate Std. Error t value Pr(>|t|) (Intercept) 2.71634 0.01702 159.638 < 2e‐16 *** fSex2 ‐0.08481 0.04030 ‐2.104 0.03548 * fSex1:fRegion2 1.41329 0.03700 38.197 < 2e‐16 *** fSex2:fRegion2 1.40180 0.06135 22.850 < 2e‐16 *** fSex1:fRegion3 2.44160 0.06674 36.586 < 2e‐16 *** fSex2:fRegion3 2.33067 0.10402 22.407 < 2e‐16 *** fSex1:fRegion5 0.40168 0.12804 3.137 0.00174 ** fSex2:fRegion5 0.43595 0.23680 1.841 0.06580 . fSex1:fRegion6 0.18366 0.10931 1.680 0.09309 . fSex2:fRegion6 0.04347 0.12612 0.345 0.73039 fSex1:fRegion7 ‐0.01634 0.10002 ‐0.163 0.87023 fSex2:fRegion7 0.05180 0.07869 0.658 0.51042 fSex1:fAntrop1 0.07868 0.09024 0.872 0.38342 fSex2:fAntrop1 0.02000 0.08364 0.239 0.81103 fSex1:fAntrop2 0.05341 0.09968 0.536 0.59216 fSex2:fAntrop2 0.12556 0.09522 1.319 0.18750 fSex1:fHabitat1 ‐0.27045 0.10968 ‐2.466 0.01377 * fSex2:fHabitat1 ‐0.33220 0.13410 ‐2.477 0.01334 * fSex1:fHabitat4 ‐0.02817 0.02173 ‐1.296 0.19503 fSex2:fHabitat4 ‐0.05856 0.04486 ‐1.305 0.19190 fSex1:fHabitat5 3.67350 0.05386 68.203 < 2e‐16 *** fSex2:fHabitat5 3.73667 0.09087 41.120 < 2e‐16 *** fSex1:fHabitat6 NA NA NA NA fSex2:fHabitat6 NA NA NA NA fSex1:fHabitat7 1.65897 0.10382 15.980 < 2e‐16 *** fSex2:fHabitat7 1.78962 0.10199 17.548 < 2e‐16 *** fSex1:fHabitat1 9 ‐0.35662 0.15667 ‐2.276 0.02295 * fSex2:fHabitat1 9 ‐0.28220 0.21976 ‐1.284 0.19927 fSex1:fHabitat2 0 NA NA NA NA fSex2:fHabitat2 0 NA NA NA NA ‐‐‐ Signif. codes: 0 ‘***’ 0. 001 ‘**’ 0. 01 ‘*’ 0 .05 ‘.’ 0 .1 ‘ ’ 1 Residual standard error: 0.2414 on 1753 degrees of freedom Multiple R‐squared: 0.9425, AdjustedR‐squared: 0.9417 F‐statistic: 1150 on 25 and 1753 DF,p‐value: < 2.2e‐16 Analysis of Variance Table Response: Elytra.Width Electronic Supplements to: Sukhodolskaya and Saveliev, Periodicum Biologorum, 2016, 118(3):273-280 DOI: 10.18054/pb.2016.118.3.3918 Df Sum Sq Mean Sq F value Pr(>F) fSex 1 15.98 15.982 2 74.18 < 2.2e‐16 * ** fSex:fRegion 10 1133.12 113.312 19 43.91 < 2.2e‐16 * ** fSex:fAntrop 4 92.11 23.029 3 95.06 < 2.2e‐16 * ** fSex:fHabitat 10 434.31 43.431 7 45.08 < 2.2e‐16 * ** Residuals 1 753 102.18 0.058 ‐‐‐ Signif. codes: 0 ‘***’ 0. 001 ‘**’ 0. 01 ‘*’ 0 .05 ‘.’ 0 .1 ‘ ’ 1 Electronic Supplements to: Sukhodolskaya and Saveliev, Periodicum Biologorum, 2016, 118(3):273-280 DOI: 10.18054/pb.2016.118.3.3918 Call: lm(formula = Pronotum.Length ~ fSex/(fRegion+ fAntrop+ fHabitat), data = cur.data, weights = Wts, contrasts= list(fRegion = ct.Region, fAntrop= ct.Antrop, fHabitat= ct.Habitat)) Residuals: Min 1Q Median 3Q M ax ‐1.2116 ‐0.1114 ‐0.0042 0 .0951 4.29 52 Coefficients: (4 not defined becauseof singularities) Estimate Std. Error t value Pr(>|t|) (Intercept) 3.803593 0.018334 207.456 < 2e‐16 *** fSex2 ‐0.040763 0.043425 ‐0.939 0.34802 fSex1:fRegion2 ‐0.070260 0.039868 ‐1.762 0.07819 . fSex2:fRegion2 ‐0.129496 0.066102 ‐1.959 0.05027 . fSex1:fRegion3 0.097967 0.071908 1.362 0.17325 fSex2:fRegion3 ‐0.066527 0.112077 ‐0.594 0.55287 fSex1:fRegion5 0.134774 0.137968 0.977 0.32878 fSex2:fRegion5 0.033473 0.255156 0.131 0.89564 fSex1:fRegion6 0.156407 0.117777 1.328 0.18435 fSex2:fRegion6 0.062170 0.135900 0.457 0.64739 fSex1:fRegion7 ‐0.220260 0.107775 ‐2.044 0.04113 * fSex2:fRegion7 ‐0.071163 0.084790 ‐0.839 0.40142 fSex1:fAntrop1 ‐0.101471 0.097236 ‐1.044 0.29684 fSex2:fAntrop1 ‐0.058000 0.090118 ‐0.644 0.51992 fSex1:fAntrop2 ‐0.134091 0.107405 ‐1.248 0.21203 fSex2:fAntrop2 ‐0.138889 0.102603 ‐1.354 0.17602 fSex1:fHabitat1 ‐0.026560 0.118180 ‐0.225 0.82220 fSex2:fHabitat1 0.003698 0.144494 0.026 0.97959 fSex1:fHabitat4 ‐0.098791 0.023416 ‐4.219 2.58e‐05 *** fSex2:fHabitat4 ‐0.142256 0.048337 ‐2.943 0.00329 ** fSex1:fHabitat5 ‐0.020833 0.058036 ‐0.359 0.71966 fSex2:fHabitat5 ‐0.093333 0.097916 ‐0.953 0.34062 fSex1:fHabitat6 NA NA NA NA fSex2:fHabitat6 NA NA NA NA fSex1:fHabitat7 ‐0.490544 0.111863 ‐4.385 1.23e‐05 *** fSex2:fHabitat7 ‐0.301840 0.109890 ‐2.747 0.00608 ** fSex1:fHabitat1 9 0.199910 0.168810 1.184 0.23648 fSex2:fHabitat1 9 ‐0.038302 0.236792 ‐0.162 0.87152 fSex1:fHabitat2 0 NA NA NA NA fSex2:fHabitat2 0 NA NA NA NA ‐‐‐ Signif. codes: 0 ‘***’ 0. 001 ‘**’ 0. 01 ‘*’ 0 .05 ‘.’ 0 .1 ‘ ’ 1 Residual standard error: 0.2601 on 1753 degrees of freedom Multiple R‐squared: 0.1093, AdjustedR‐squared: 0.09662 F‐statistic: 8.607 on 25 and 1753 DF,p‐value: < 2.2e‐16 Analysis of Variance Table Response: Pronotum.Length Electronic Supplements to: Sukhodolskaya and Saveliev, Periodicum Biologorum, 2016, 118(3):273-280 DOI: 10.18054/pb.2016.118.3.3918 Df Sum Sq Mean Sq F value Pr(>F) fSex 1 2.169 2.16890 32 .0481 1. 754e‐08 * ** fSex:fRegion 10 1.534 0.15338 2 .2663 0.01245 * fSex:fAntrop 4 6.098 1.52440 22 .5248 < 2.2e‐16 * ** fSex:fHabitat 10 4.761 0.47612 7 .0353 6. 512e‐11 * ** Residuals 1 753 118.637 0.06768 ‐‐‐ Signif. codes: 0 ‘***’ 0. 001 ‘**’ 0. 01 ‘*’ 0 .05 ‘.’ 0 .1 ‘ ’ 1 Electronic Supplements to: Sukhodolskaya and Saveliev, Periodicum Biologorum, 2016, 118(3):273-280 DOI: 10.18054/pb.2016.118.3.3918 Call: lm(formula = Pronotum.Width ~ fSex/(fRegion +fAntrop+ fHabitat), data = cur.data, weights = Wts, contrasts= list(fRegion = ct.Region, fAntrop= ct.Antrop, fHabitat= ct.Habitat)) Residuals: Min 1Q Median 3Q Max ‐0.85324 ‐0.129 88 0.00564 0.12969 1.19451 Coefficients: (4 not defined becauseof singularities) Estimate Std. Error t value Pr(>|t|) (Intercept) 4.144138 0.017232 240.493 < 2e‐16 *** fSex2 ‐0.133123 0.040814 ‐3.262 0.001129 ** fSex1:fRegion2 ‐0.281175 0.037470 ‐7.504 9.79e‐14 *** fSex2:fRegion2 ‐0.277682 0.062127 ‐4.470 8.34e‐06 *** fSex1:fRegion3 ‐0.138391 0.067583 ‐2.048 0.040738 * fSex2:fRegion3 ‐0.266688 0.105337 ‐2.532 0.011436 * fSex1:fRegion5 0.490086 0.129670 3.779 0.000162 *** fSex2:fRegion5 0.421508 0.239811 1.758 0.078979 . fSex1:fRegion6 0.115862 0.110694 1.047 0.295390 fSex2:fRegion6 0.238985 0.127727 1.871 0.061503 . fSex1:fRegion7 ‐0.394138 0.101294 ‐3.891 0.000104 *** fSex2:fRegion7 ‐0.144349 0.079691 ‐1.811 0.070256 . fSex1:fAntrop1 0.070588 0.091388 0.772 0.439981 fSex2:fAntrop1 ‐0.072000 0.084698 ‐0.850 0.395397 fSex1:fAntrop2 0.061364 0.100945 0.608 0.543340 fSex2:fAntrop2 ‐0.066667 0.096433 ‐0.691 0.489451 fSex1:fHabitat1 ‐0.330748 0.111072 ‐2.978 0.002943 ** fSex2:fHabitat1 ‐0.094327 0.135804 ‐0.695 0.487410 fSex1:fHabitat4 ‐0.138836 0.022008 ‐6.308 3.56e‐10 *** fSex2:fHabitat4 ‐0.129501 0.045430 ‐2.851 0.004415 ** fSex1:fHabitat5 0.099537 0.054546 1.825 0.068195 . fSex2:fHabitat5 0.006667 0.092027 0.072 0.942258 fSex1:fHabitat6 NA NA NA NA fSex2:fHabitat6 NA NA NA NA fSex1:fHabitat7 ‐0.846268 0.105135 ‐8.049 1.52e‐15 *** fSex2:fHabitat7 ‐0.585777 0.103281 ‐5.672 1.65e‐08 *** fSex1:fHabitat1 9 ‐0.236336 0.158658 ‐1.490 0.136512 fSex2:fHabitat1 9 ‐0.122327 0.222551 ‐0.550 0.582624 fSex1:fHabitat2 0 NA NA NA NA fSex2:fHabitat2 0 NA NA NA NA ‐‐‐ Signif. codes: 0 ‘***’ 0. 001 ‘**’ 0. 01 ‘*’ 0 .05 ‘.’ 0 .1 ‘ ’ 1 Residual standard error: 0.2445 on 1753 degrees of freedom Multiple R‐squared: 0.3075, AdjustedR‐squared: 0.2976 F‐statistic: 31.14 on 25 and 1753 DF,p‐value: < 2.2e‐16 Analysis of Variance Table Response: Pronotum.Width Electronic Supplements to: Sukhodolskaya and Saveliev, Periodicum Biologorum, 2016, 118(3):273-280 DOI: 10.18054/pb.2016.118.3.3918 Df Sum Sq Mean Sq F value Pr(>F) fSex 1 9.850 9.8496 16 4.762 < 2.2e‐16 * ** fSex:fRegion 10 13.897 1.3897 2 3.247 < 2.2e‐16 * ** fSex:fAntrop 4 13.674 3.4185 5 7.183 < 2.2e‐16 * ** fSex:fHabitat 10 9.117 0.9117 1 5.250 < 2.2e‐16 * ** Residuals 1 753 104.796 0.0598 ‐‐‐ Signif. codes: 0 ‘***’ 0. 001 ‘**’ 0. 01 ‘*’ 0 .05 ‘.’ 0 .1 ‘ ’ 1 Electronic Supplements to: Sukhodolskaya and Saveliev, Periodicum Biologorum, 2016, 118(3):273-280 DOI: 10.18054/pb.2016.118.3.3918 Call: lm(formula = Head.Length ~fSex/(fRegion + fAntrop + fHabitat), data = cur.data, weights = Wts, contrasts= list(fRegion = ct.Region, fAntrop= ct.Antrop, fHabitat= ct.Habitat)) Residuals: Min 1Q Median 3Q Max ‐1.03269 ‐0.129 06 0.02845 0.13896 1.85556 Coefficients: ( 4 not defin ed because of singu larities) Estimate Std. Error t value Pr(>|t|) (Intercept) 2.869763 0.018684 153.597 < 2e‐16 *** fSex2 ‐0.158036 0.044253 ‐3.571 0.000365 *** fSex1:fRegion2 ‐0.225318 0.040627 ‐5.546 3.37e‐08 *** fSex2:fRegion2 ‐0.078393 0.067361 ‐1.164 0.244672 fSex1:fRegion3 ‐0.888531 0.073278 ‐12.126 < 2e‐16 *** fSex2:fRegion3 ‐0.920849 0.114212 ‐8.063 1.37e‐15 *** fSex1:fRegion5 ‐0.249986 0.140596 ‐1.778 0.075570 . fSex2:fRegion5 ‐0.152653 0.260017 ‐0.587 0.557220 fSex1:fRegion6 ‐0.269763 0.120021 ‐2.248 0.024723 * fSex2:fRegion6 0.013273 0.138489 0.096 0.923656 fSex1:fRegion7 ‐0.569763 0.109829 ‐5.188 2.38e‐07 *** fSex2:fRegion7 ‐0.270060 0.086405 ‐3.126 0.001804 ** fSex1:fAntrop1 0.208824 0.099088 2.107 0.035220 * fSex2:fAntrop1 0.138000 0.091834 1.503 0.133095 fSex1:fAntrop2 0.034091 0.109451 0.311 0.755478 fSex2:fAntrop2 ‐0.008889 0.104558 ‐0.085 0.932260 fSex1:fHabitat1 0.143768 0.120431 1.194 0.232725 fSex2:fHabitat1 0.279122 0.147247 1.896 0.058176 . fSex1:fHabitat4 ‐0.070412 0.023862 ‐2.951 0.003212 ** fSex2:fHabitat4 ‐0.123355 0.049257 ‐2.504 0.012360 * fSex1:fHabitat5 ‐0.431944 0.059141 ‐7.304 4.23e‐13 *** fSex2:fHabitat5 ‐0.673333 0.099781 ‐6.748 2.03e‐11 *** fSex1:fHabitat6 NA NA NA NA fSex2:fHabitat6 NA NA NA NA fSex1:fHabitat7 ‐0.412459 0.113994 ‐3.618 0.000305 *** fSex2:fHabitat7 ‐0.315253 0.111983 ‐2.815 0.004929 ** fSex1:fHabitat1 9 0.169945 0.172026 0.988 0.323338 fSex2:fHabitat1 9 0.421122 0.241303 1.745 0.081124 . fSex1:fHabitat2 0 NA NA NA NA fSex2:fHabitat2 0 NA NA NA NA ‐‐‐ Signif. codes: 0 ‘***’ 0. 001 ‘**’ 0. 01 ‘*’ 0 .05 ‘.’ 0 .1 ‘ ’ 1 Residual standard error: 0.2651 on 1753 degrees of freedom Multiple R‐squared: 0.3635, AdjustedR‐squared: 0.3544 F‐statistic: 40.04 on 25 and 1753 DF,p‐value: < 2.2e‐16 Analysis of Variance Table Response: Head.Length Electronic Supplements to: Sukhodolskaya and Saveliev, Periodicum Biologorum, 2016, 118(3):273-280 DOI: 10.18054/pb.2016.118.3.3918 Df Sum Sq Mean Sq F value P r(>F) fSex 1 12.391 12.3906 17 6.3040 < 2e‐16 *** fSex:fRegion 10 45.358 4.5358 6 4.5391 < 2e‐16 *** fSex:fAntrop 4 0.476 0.1190 1.6926 0 .1490 fSex:fHabitat 10 12.124 1.2124 1 7.2506 < 2e‐16 *** Residuals 1 753 123.200 0.0703 ‐‐‐ Signif. codes: 0 ‘***’ 0. 001 ‘**’ 0. 01 ‘*’ 0 .05 ‘.’ 0 .1 ‘ ’ 1 Electronic Supplements to: Sukhodolskaya and Saveliev, Periodicum Biologorum, 2016, 118(3):273-280 DOI: 10.18054/pb.2016.118.3.3918 Call: lm(formula = Eye.Distance~ fSex/(fRegion + fAntrop +fHabitat), data = cur.data, weights = Wts, contrasts= list(fRegion = ct.Region, fAntrop= ct.Antrop, fHabitat= ct.Habitat)) Residuals: Min 1Q Median 3Q Max ‐0.60100 ‐0.083 35 ‐0.00340 0.06650 1.59900 Coefficients: (4 not defined becauseof singularities) Estimate Std. Error t value Pr(>|t|) (Intercept) 2.229185 0.010865 205.176 < 2e‐16 *** fSex2 ‐0.040080 0.025733 ‐1.558 0.119529 fSex1:fRegion2 0.033778 0.023625 1.430 0.152970 fSex2:fRegion2 ‐0.089105 0.039171 ‐2.275 0.023040 * fSex1:fRegion3 ‐0.027803 0.042612 ‐0.652 0.514181 fSex2:fRegion3 ‐0.096967 0.066416 ‐1.460 0.144466 fSex1:fRegion5 0.082963 0.081758 1.015 0.310372 fSex2:fRegion5 0.093033 0.151202 0.615 0.538447 fSex1:fRegion6 0.090815 0.069793 1.301 0.193363 fSex2:fRegion6 0.210895 0.080532 2.619 0.008901 ** fSex1:fRegion7 0.070815 0.063866 1.109 0.267672 fSex2:fRegion7 0.102561 0.050245 2.041 0.041380 * fSex1:fAntrop1 0.041176 0.057621 0.715 0.474944 fSex2:fAntrop1 0.132000 0.053403 2.472 0.013538 * fSex1:fAntrop2 ‐0.029545 0.063647 ‐0.464 0.642555 fSex2:fAntrop2 0.073333 0.060801 1.206 0.227937 fSex1:fHabitat1 0.023618 0.070032 0.337 0.735975 fSex2:fHabitat1 ‐0.082138 0.085625 ‐0.959 0.337555 fSex1:fHabitat4 ‐0.001841 0.013876 ‐0.133 0.894482 fSex2:fHabitat4 0.019933 0.028644 0.696 0.486582 fSex1:fHabitat5 0.130787 0.034391 3.803 0.000148 *** fSex2:fHabitat5 0.060000 0.058024 1.034 0.301250 fSex1:fHabitat6 NA NA NA NA fSex2:fHabitat6 NA NA NA NA fSex1:fHabitat7 0.177345 0.066288 2.675 0.007535 ** fSex2:fHabitat7 ‐0.020109 0.065119 ‐0.309 0.757510 fSex1:fHabitat1 9 0.077441 0.100035 0.774 0.438952 fSex2:fHabitat1 9 ‐0.124138 0.140320 ‐0.885 0.376452 fSex1:fHabitat2 0 NA NA NA NA fSex2:fHabitat2 0 NA NA NA NA ‐‐‐ Signif. codes: 0 ‘***’ 0. 001 ‘**’ 0. 01 ‘*’ 0 .05 ‘.’ 0 .1 ‘ ’ 1 Residual standard error: 0.1542 on 1753 degrees of freedom Multiple R‐squared: 0.1003, AdjustedR‐squared: 0.08745 F‐statistic: 7.816 on 25 and 1753 DF,p‐value: < 2.2e‐16 Analysis of Variance Table Response: Eye.Distance Electronic Supplements to: Sukhodolskaya and Saveliev, Periodicum Biologorum, 2016, 118(3):273-280 DOI: 10.18054/pb.2016.118.3.3918 Df Sum Sq Mean Sq F v alue Pr(>F) fSex 1 0.954 0.95429 40. 1547 2.9 76e‐10 ** * fSex:fRegion 10 1.643 0.16433 6. 9148 1.0 90e‐10 ** * fSex:fAntrop 4 1.364 0.34100 14. 3485 1.5 70e‐11 ** * fSex:fHabitat 10 0.682 0.06819 2. 8692 0. 001487 ** Residuals 1 753 41.661 0.02377 ‐‐‐ Signif. codes: 0 ‘***’ 0. 001 ‘**’ 0. 01 ‘*’ 0 .05 ‘.’ 0 .1 ‘ ’ 1 Electronic Supplements to: Sukhodolskaya and Saveliev, Periodicum Biologorum, 2016, 118(3):273-280 DOI: 10.18054/pb.2016.118.3.3918 S5 Effects of environmental factors on elytra length variation in P. niger, results of linear modeling Factor Contribution of factor into the trait deviation Contribution of factor into the trait mean Females Males Females Males Confidence interval Mean of Confidence interval Mean of Confidence interval Trait mean Confidence interval Trait mean limits the limits the limits limits deviation deviation Left Right Left Right Left Right Left Right 2,5% 97,5% 2,5% 97,5% 2,5% 97,5% 2,5% 97,5% Sverdlovsk region -0.98 -0.62 -0.8 -1.12 -0.52 -0.82 10.2 10.52 10.36 9.48 9.96 9.72 Kemerovo region -0.51 0.14 -0.18 -1.23 -0.22 -0.73 10.64 11.31 10.98 9.28 10.35 9.81 Udmurtia -0.85 0.4 -0.23 -1.71 0.59 -0.56 10.3 11.56 10.93 8.82 11.15 9.98 Mariy El -1.39 -0.33 -0.86 -0.93 0.3 -0.31 9.77 10.83 10.3 9.64 10.81 10.22 Cis-Ural -1.95 -0.97 -1.46 -1.07 -0.31 -0.69 9.22 10.18 9.7 9.51 10.19 9.85 Urban -0.57 0.31 -0.13 -0.35 0.46 0.06 10.58 11.47 11.03 10.15 11.04 10.6 Suburban -0.49 0.48 0 -0.64 0.29 -0.18 10.66 11.65 11.16 9.87 10.86 10.36 Meadow -0.9 0.17 -0.37 -0.57 0.74 0.09 10.27 11.32 10.79 10 11.25 10.63 Elm -0.38 -0.17 -0.28 -0.54 -0.1 -0.32 10.82 10.95 10.88 10.09 10.35 10.22 Jak -0.02 0.5 0.24 -0.12 0.77 0.32 11.12 11.67 11.4 10.39 11.34 10.86 Lime -2.08 -1.07 -1.58 -1.5 -0.51 -1 9.08 10.08 9.58 9.07 10 9.53 Lawn -0.71 0.82 0.05 -0.94 1.2 0.13 10.46 11.97 11.21 9.61 11.72 10.67
Journal
Periodicum Biologorum – Unpaywall
Published: Sep 30, 2016