The incubators, with almost constant temperature(±0,5°C) and constant darkness,were set at 4°C intervals: 4, 8,12,16,20 and24°C. A cold room at approximately 2°C(±1 0c) was also used. The eggs were inspecteddaily for hatching until all eggs had hatchedor the remaining eggs were either discolouredor destroyed by fungi. The incubationtime of the whole egg batch was consideredto be the time from the egg laying until50% of the eggs that eventually would hatchhad hatched (Brittain 1977).Table 1. Number of eggs laid (N) and hatched(N'), %hatching, mean incubation time and variationin incubation time for eggbatches of C. sehilleri.Temp. N N' Hatch. % Mean.ink.timeVar.2 69 0 04 113 54 47,8 77 68-9369 5 7,2 68 67-69682 668 97,9 73 61-87132 56 42,4 71 63-858 334 329 98,5 38 30-45832 811 97,5 39 30-55525 504 96,0 37 30-4870 14 20,0 38 38-4212 182 180 98,9 20 19-27295 294 99,7 18 15-254562392486,738,7162015-1718-22360 320350 19088,954,3232218-2619-3016 119 119 100,0 11 9-15899 894 99,4 15 11-25186 157 84,4 14 10-1820 137 137 100,0 11 9-15266 264 99,3 11 9-1350 48 96,0 11 10-1662 62 100,0 9 7-1224 19 11 57,9 10 9-14650 63 9,7 13 9-1513 4 30,8 12 11-21N =6521 N' =524742'DO! "':50I"".:"'. .\... :lJ \ .4 8 12 18 20 24Fig. 1. The mean incubation time of egg batches ofC. sehilleri plotted on log. paper with regressionline.RESULTSThe results of the egg incubation studies aregiven in Tab. 1, and pooled for each temperaturein Fig. 1. The egg incubation time whichwas clearly dependent on temperature, decreasedas the temperature increased. The eggsdid not hatch at 2°C and only a few hatchedat 24°C. At this high temperature it seemsthat the incubation time increased again, butthis might be an artifact caused by the lownumber of eggs. If the data from 24°C areignored, the rest fit very well the regressionline Y =429.T-l,24, (r = 0,985) where Y istime in days and T is temperature in QC.The eggs hatched with no sign of delayedhatching with the possible exception of 24°C.The hatching success varied with temperature(see Tab. 1), and also for different eggbatches. The highest hatching success was inthe tempt:rature interval of 8-20°C, but oneegg batch at 4°C also had a very high hatchingsuccess.The egr;s needed on average 264 day-degreesabove O°C to hatch, but the variationwas big; 120-500 day-degrees (Fig. 2). Thelowest heatsum was needed between 12 and20°C.The method used does not allow an assessmentof the number ofeggs deposited in each
· soo8 12 16 20 24Fig. 2. Day-degrees needed for eggs at differenttemperatures. The stippled line is the mean for alltemperatures. The mean value for each temperatureis also indicated.egg batch from each female, since severalfemales could have laid eggs in the same dishat the same time.Newly laid eggs did not show any visiblesign of an embryo.DISCUSSIONThe egg incubation time of C. schilleri isclearly temperature dependent. Other factorsinfluencing the incubation time are individualvariation within the egg batch and variationbetween egg batches from different females,as well as differences between the differentegg batches from a single female. Thesame pattern is revealed in the study of Brittain(1977) on Taeniopteryx nebulosa (L)(Taeniopterygidae) and the studies of Saltveit(1977), Brittain (1978) and Rekstad(1979) on different species of Nemouridae,though with different inclination of the regressionline for the different species. Lillehammer(l975b) found different incubationtime for different egg batches at the sametemperature for several species of Capniidae,Nemouridae and Leuctridae. Late in thisstudy I started wondering wether the size ofthe egg batch had any influence on the incubationtime and especially on the hatchingsuccess, since some of the smallest batchesdiffered a little from the others. This might bebecause these batches were the last ofseveralbatches from the same female, but with smallerresources. It would be interesting to followthis line of investigation further.Probably there are also differences betweendifferent populations regarding the relationshipbetween incubation time and temperature.Brittain (1978) and Rekstad (1979),who investigated populations of Nemurellapictetii Klapalek from a high mountain siteand a lowland site respectively, found somedifferences. But Brittain et al. (1984) foundthat population differences made no significantcontribution to variation in egg incuba:ion time in Capnia atra. Probably the results)fthis study are generally applicable to otherJopulations of C. schilleri, but some variationis to be expected. The only study that hasbeen made of another population is the studyof Berthelemy (1973) from Tunisia, but heused fluctuating temperatures, so it is difficultto make a direct comparison.The high hatching success at very diversetemperatures would indicate that C. schillericould thrive under very different environmentalconditions, no one temperature beingclearly optimal for the egg stage. Since therewas no sign of diapause or delayed hatchingor ovovivipary, the regulation of the lifecycle to suit the different conditions the specieswill meet must be in other stages of thelife cycle, namely the nymphal stage. Berthelemy(1973) says that C. schilleri in Tunisiahas a diapause in the larval stage during thehot summer.The egg development of C. schilleri inNorway is quick; 6 eggs hatched after only 7days in one egg batch at 20°C. Since the eggswere inspected only once every day there is apossibility that these eggs were laid nearlyone day before the batch was registered andhatched just before the first nymphs werediscovered. This could mean that the realjevelopment time is 8 days and not 7. Thislpplies to all the eggs on all temperatures of;ourse, but is a relatively greater source of~rror at the highest temperatures. To have~xact development time one would have toinspect the eggs much more often, but this isnot always possible.ACKNOWLEDGEMENTSMany thanks are due to Curator Or. PhiI. A.Lillehammer for supervising the study andgiving good advice, to Cand. real. Jan Brekkefor help with the statistics and to Cand. phil.Knut Pettersen for correcting the English.REFERENCESBerthelemy, C. 1973. Donnees preliminaires surles Plecopteres de Tunisie. Verh. Internal. Ver.Theor. Angew. Limnol. 18, 1544-1548.43
- Page 1 and 2: No. 11987SER. B VOL. 34NO. 1Norwegi
- Page 3 and 4: Professor Ole A. Srether 50 yearsFo
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- Page 14 and 15: Sverre Kobro, Carl Fredrik Liihr, R
- Page 16 and 17: -.Occurrence and life cycle of Dino
- Page 18 and 19: width of 1 2 3 4pronotum n: 19 13 I
- Page 20 and 21: LITTERAT.UREAubert, J. 1946. Les Pl
- Page 22 and 23: Fig. 1. Brachycaudus (Acaudus) popu
- Page 24: Nymphal development and food consum
- Page 27 and 28: espectively. At 20°C, mean number
- Page 29 and 30: than P. mali. Upon examination of t
- Page 31 and 32: The first record of Thaumalea ve"al
- Page 33 and 34: Bibio nigriventris Haliday, 1833 (D
- Page 35 and 36: ker 1 ~ 27 June 1873 (ZMO 11293). P
- Page 37 and 38: Megamerina dolium (Fabricius, 1805)
- Page 39 and 40: New Norwegian Empididae (s.str.) (D
- Page 41 and 42: A,H. obscura MeigenRY, Rennes0Y: F0
- Page 43: Influence of temperature on the egg
- Page 47: Distribution and seasonal abundance
- Page 50 and 51: Table 2. Percentage composition of
- Page 52 and 53: ut from a zoogeographical point of
- Page 55 and 56: Table I. Tipulidae species recorded
- Page 57 and 58: area, Torne Lappmark (Tjeder 1978).
- Page 59 and 60: Twelve species of Neuropteroidea an
- Page 61 and 62: Table I. Number of specimens (males
- Page 63 and 64: etween summer and autumn. H. stigma
- Page 65: Distribution and seasonal abundance
- Page 68 and 69: Table I. Number of individuals of v
- Page 70 and 71: ,[Table 3. Relative abundance of th
- Page 72 and 73: ,(Table 6. Number ofspecies collect
- Page 74 and 75: there. This is a northern species,
- Page 76 and 77: denticulata, Onychiurus armatus (Tu
- Page 78 and 79: Kallvellsj0enStroplsj0enKongsvoll B
- Page 80 and 81: Faro. PsilidaeMaterial of Psilidae
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- Page 84 and 85: Table 1. Habitat/host plants for th
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- Page 88 and 89: Sericothrips abnormis (Karny, 1909)
- Page 90: collected from birch in Oslo, in Tr
- Page 93 and 94: Maltbrek, J. 1932. Frynsevinger. Da
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--_..- ---~---'Aug. 1977, a male Ap
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zur Kenntnis der Thermopilie bei Sp
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