THE BREEDING BIOLOGY OF THE BLACK-FACED DIOCH QUELEA QUELEA IN NIGERIA

A study of the breeding biology of Quelea quelea in Nigeria, and particularly at a large breeding colony near Lake Chad, showed that losses of eggs and young were extremely small. 95% of eggs laid hatched successfully, and 87% give rise to fledglings. Nestling deaths were density-dependent and apparently due to starvation.
The incubation period was 10 days or less. By day, eggs were heated to 34°- 37° C. by the sun; at night the females incubated. The nestlings were initially fed mainly on insects, their diet gradually changing to one of seeds—mostly of the grass Echinochloa pyramidalis . The deep body temperatures of young birds were determined. It is suggested that the nestlings left the nest after, on average, 11¹/₂ days to escape intolerable temperature conditions in the nest.
Fat reserves were accumulated by nestlings and fledglings, and were utilized when the young became independent. The adults put on fat during the incubation period and lost it during the time spent feeding nestlings.
It is concluded that the most common clutch-size of Q. quelea , which is everywhere three, corresponds to the largest number of young the parents can normally nourish. This conforms to Lack's theory on the significance of clutch-size, and gives no support to Skutch's opinion that the theory does not apply to tropical birds.     

BREEDING BIOLOGY OF THE BEARDED VULTURE IN SOUTHERN AFRICA,PART I: THE PRELAYING AND INCUBATION PERIODS

Brown, C. J. 1990. Breeding biolo of the Bearded Vulture in southern Africa, Part I: The pre-laying and incubation periods. Ostrich 61: 24–32.

In southern Africa the Bearded Vulture Gpaetus barbatus lays its eggs in mid-winter. between the second half of May and the first week of July. Pairs became more active in their nesting areas about six weeks before laying and usually roosted there at night. Courtship flights were less frequent and demonstrative than in Eurasian birds and took place mainly in the late afternoons. During the pre-laying period most nest visits (77%) were to bring nesting material, 92% by the male. All nesting material was arranged by the female. Copulation was always preceded by allopreening, and occurred most frequently in the mornings. No copulation or courtship display took place after the first egg had been laid. Of 18 clutches, 16 (89%) contained two eggs and the remainder one egg. The laying interval was usually 3–5 days (range 2–9 days). Incubation started with the first egg and was evenly shared by both parents during the day, but only the female incubated at night, individual pairs maintained distinctive nest attendance and foraging period timetables, which allowed sufficient time for self-foraging by both parentes. No food was brought into the nest during the pre-laying and incubation periods, but in some pairs food was cached in nearby potholes in cliffs. The incubation period was 56–57 days.     

FURTHER OBSERVATIONS ON THE BIOLOGY OF THE CABBAGE ROOT FLY, ERIOISCHIA BRASSJCAE BCHÉ

In 1951, eggs of Erioischia brassicae were first found in the field on 2 May, and the peak period of egg-laying occurred 19–31 May. This was up to a month later than in the period 1948-50.
The periodic removal and examination of the surface soil showed that eggs of E. brassicae were continuously present on the host plants from mid-June to early November. Plants under observation during this period showed an average of 285 eggs per plant and other plants exposed to attack from July to November showed an average of 162 eggs per plant. Peak periods of egg-laying, as indicated by numbers of eggs per plant per day, occurred in late June and early July, in mid-August and, to a less extent, in the first half of October. The plants showed no increase in the rate of infestation as the season advanced, although E. brassicae has a reproductive capacity of about 100 eggs per female and three to four generations a year.
The difference between the observed egg populations and pupal populations indicated that E. brassicae had a heavy mortality rate in its immature stages. The condition of puparia showed that the species was subject to a high degree of natural control, a fact for consideration when direct control measures are formulated.
Pupal diapause extending from October 1949 to May 1951 was observed in one specimen of E. brassicae and from October 1949 to August 1951 in one specimen of its Hymenopterous parasite, Trybliographa rapae Westw.
Tests with tar-oil winter wash showed that at a concentration of 1 1/4% it killed eggs of Erioischia brassicae and repelled gravid females for approximately a week. Laboratory tests with BHC indicated that it had no adverse effects on the eggs but was larvicidal.     

高黎贡山白尾梢虹雉繁殖生态观察

2002-2004年连续3个春季在高黎贡山自然保护区对白尾梢虹雉(Lophophorus sclateri)的繁殖习性进行了观察,对白尾梢虹雉的巢、卵和雏鸟进行了详细描述.在高黎贡山南段,白尾梢虹雉的产卵孵化始于3月底,止于5月初,窝卵数为2～3枚,孵卵期为28 d.窝卵数低、适宜巢址缺乏有可能是白尾梢虹雉种群增长缓慢...     

Geographical variation in Japan in egg development of the mayfly, Ephoron shigae (Ephemeroptera: Polymitarcyidae)

1. The effect of temperature on embryonic development was compared in four populations, two bisexual and two unisexual, of Ephoron shigae , including one each near the northern and southern periphery of the species range in Japan.
2. Eggs from every population were chilled at 4, 8 or 12 °C for diapause development after 50 days at 20 °C for pre-diapause development (experiment I). Some eggs hatched during chilling at 8 °C or 12 °C, whereas no eggs hatched at 4 °C. The rate of hatching in a given condition of chilling was higher for the eggs from warmer winter environments.
3. Chilling at 4 or 8 °C effectively facilitated diapause development. Chilling at 12 °C was, in general, not so effective, but relatively effective for the eggs from warmer winter environments.
4. Eggs were incubated at 8, 12, 15 or 20 °C after chilling at 4 °C to examine the effect of temperature on post-diapause development (experiment II). The eggs incubated at higher temperature after chilling hatched quicker and more synchronously and had higher hatching success.
5. The relationship between temperature and the days required for hatching after chilling was well described by the power function. There was no significant difference in the slope of the regression lines (i.e. temperature dependency) among local populations. However, a longer time was required for hatching at a given temperature for the population from the colder winter environment.
6. There was no detectable difference in the observed intraspecific variations between unisexual and bisexual populations.     

人工饲养条件下黄额闭壳龟的繁殖行为研究

2017—2019年在广西壮族自治区桂林市永福县对7只性成熟(5雌2雄)黄额闭壳龟Cuora galbinifrons的交配与繁殖进行了观察研究,记录人工养殖条件下亲龟的生活、交配及繁殖习性,结合相关研究报导,调整亲龟饲养及龟卵孵化方法,在人工养殖条件下成功繁殖出F₁代个体。结果表明,试验亲龟生长状况良好,体质量年平均增长率达6.37%,交配高峰期为5—6月,产卵期为6—7月。共获得5枚受精卵,2次产卵之间积温为197 230～207 955℃·h,并成功孵化出F₁代稚龟3只,龟卵孵化时间为118～136 d,孵化积温为76 464～88 128℃·h,孵化率60.00%。本研究为黄额闭壳龟的人工饲养繁殖提供了理论依据和实践基础。     

Influence of temperature on hatching of winter eggs of fruit-tree red spider mite, Panonychus ulmi (Koch)

The effects of the duration and degree of chilling, and the temperature of incubation, on hatching of winter eggs of Panonychus ulmi (Koch) were investigated. For chilling, 0°C and 5°C were more effective than — 5° and 9°, and the limits for the reaction were close to — 10° and 15°. As the chilling period was increased from 60 to 200 days, the percentage hatch on incubation at 21° increased, and the mean incubation time and its variance decreased. Before the maximum effect of chilling was achieved, percentage hatch on incubation at 9° and 15° was higher than at 21°; 27° was lethal to most winter eggs though not to summer eggs. After chilling, the later stages of diapause development could occur at temperatures from 0° to 21°₎ i.e. above and below the threshold temperature for morphogenesis, 6–7° in both winter and summer eggs. Diapause development cannot, therefore, be a unitary process. The significance of the results is discussed in relation to forecasting the time of hatch in the field, and to the phenological aspects of hatching in the spring.     

Biology and bionomics in Scotland of Anthocoris gallarum-ulmi

Abstract. 1. Observations were made on the biology of Anthocoris gallarumulmi De Geer (Hemiptera - Heteroptera: Anthocoridae) in West Central Scotland from 1973 until 1975. The life cycle was intimately linked with those of its principal prey species Schizoneura ulmi and S.patchae , leaf roll-gall aphids, and elm, their primary host ( Ulmus sp.).
2. Overwintered adults emerged in late April/May and could be found on a number of early flowering tree species, before congregating on elm in late May/June. This population was univoltine and exhibited obligatory female reproductive diapause.
3. Overwintered females emerged already mated but the subsequent pre-oviposition period was 25 days and oviposition period 27 days. Ova were deposited only in close association with galls of S.ulmi and Spatchae , and behavioural variations were shown between sites. Fecundity was c . 16 ova per female.
4. The incubation period was c . 8 days with the subsequent period of larval development 38–53 days, during which time the diet was almost exclusively either S.ulmi or S.patchae . Intergall migration was characteristic of post second instar larvae, which resulted in the concentration of fifth instar larvae and adults in a limited number of galls. It was during this period of local high population density that mating occurred.
5. Adults left elm within 14 days of imaginal ecdysis and thereafter, until overwintering, were recorded in only very low numbers from a range of tree, shrub and herb species.
6. Overwintering adults selected as hibernacula the bark of four tree species but principally Acer pseudoplatanus and Quercus robor . Females required a period of at least 75 days of cold 'shock' to terminate reproductive diapause.
7. Mortality among males surviving to spring emergence was 67%.     

BREEDING OF THE GREY WARBLER GERYGONE IGATA AT KAIKOURA, NEW ZEALAND

I studied the breeding of Grey Warblers Gerygone igata (Muscicapidae: Acanthizinae) in forest near Kaikoura, New Zealand, between 1976 and 1979. Only males sang and singing occurred all year. From late July to January pairs defended self-contained territories of 0·25–1·73 ha but they occupied larger home ranges when not breeding. Territorial adults were strictly sedentary all year. The average annual mortality of breeding adults was 18·5% and the predicted life-expectancy 4·9 years, which is remarkable in a bird weighing 6–7 g. The breeding season from first building to last fledging was six months long and it began early. Exceptionally, Grey Warblers may build and lay before the shortest day. As the season progressed warblers nested lower on average, both in absolute terms and relative to the tree nested in and canopy at the site. Warblers built in 7–27 days then delayed up to eight days before laying. Only females built and at no stage of breeding did males feed their mates. Both sexes fed the young. Grey Warblers laid for 15–16 weeks of the year and first clutches were laid asynchronously during 5–6 weeks. Eggs of a clutch appeared at two-day intervals and each egg weighed 1·5 g when fresh (23% of mean adult weight). Clutch size was nearly constant (mean 3·9, mode 4, range 3–5). The incubation period was 17–21 days (mean 19·5 days) and the nestling period 15–19 days (mean 17·2 days). On average the clutch hatched over 1·4 days, even though incubation commenced with the laying of the last egg. Nestlings reached maximum weight on Days 13–14 on average and then receded in weight by 4%, apparently through loss of water. All healthy nestlings exceeded mean adult weight during development by up to 39%. Nestlings from broods of two were at first lighter on average than those from larger broods, but in the second half of the nestling period twins were significantly the heaviest. Grey Warblers were fed for 28–35 days after fledging and they survived well while dependent on parents. Fledglings dispersed up to 3 km or more at independence and only 5% per annum joined the breeding population. Of nests that received eggs, 42% produced at least one fledgling. On average each breeding adult raised 2·0 fledglings per season. Of 265 eggs in 73 nests 70% hatched and 38% produced fledglings. Of 185 nestlings 54% fledged. Probably the main cause of mortality of eggs and nestlings was predation by introduced rodents and mustelids. Grey Warblers raise two small broods slowly during a long breeding season, rather than investing in one large quickly-reared brood. In New Zealand's mild climate the warbler's food supply may not decline severely in winter, and the population of warblers may remain so close to the limit set by food that extra for breeding is hard to obtain. Thus the breeding strategy may be adapted to a restricted food supply.     

BREEDING BIOLOGY OF THE GREY-FACED PETREL PTERODROMA MACROPTERA GOVLDI

The Grey-faced Petrel is a non-migratory winter breeder whose reproductive season occupies 9–10 months. Males spend more time in the burrows than females during the courtship period. Some females keep company with strange males, and may be fertilized by them, but subsequently share incubation with their mate of the previous year. The duration of the pre-laying absence of females is about two months, and of the pre-incubation absence of males about seven weeks. Since copulation is presumed to occur before this absence, these petrels seem to have evolved prolonged viability of the spermatozoa, though ovulation may take place some time before laying. Eggs are laid in late June or July but chicks are rarely reared from eggs laid after 14 July; effective laying thus lasts three weeks. The single egg is about 15·5% of the female's weight; she may be able to exert slight control over timing of oviposition. She may be required to incubate, if capable, for up to 14 days from laying but the male takes over, on average, after four days. There are three main incubation spells of 17 days' average duration, two by the male. These are of a duration such that there is usually a change-over near hatching. Incubation lasts about 55 days. There is competition for burrows, resulting in two-egg nests. Norway Rats take unattended eggs and young chicks and scavenge, but their predation (less than 10–35% of chicks per year) is not considered to be endangering the population. After initially more frequent feeds, chicks are fed approximately once a week by each parent. They do not become much heavier than adults and the growth rate is slow: about 120 days to departure. The ability to begin breeding in winter, atypical of petrels in this region, may be facilitated by three factors: improved availability of food resulting from longer nocturnal feeding time and reduced inter-specific competition; the ability to lay fertile eggs two months or more after copulation; and the brevity of the non-breeding season due to the relative proximity of a sufficient food supply.     

Interspecific and intraspecific variations in egg hatching for British populations of the stoneflies Siphonoperla torrentium and Chloroperia tripunctata (Plecoptera: Chloroperiidae)

SUMMARY 1. The objective was to compare variations in egg hatching between the two species (interspecific variations) and between populations of the same species (intraspecific variations). There were significant interspecific, but not intraspecific, differences in female size, adult life-span, egg production, hatching success, incubation periods and hatching periods.
2. The optimum temperature for hatching success within the range 3.8–22.1°C in the laboratory and the range over which at least 50% of the eggs hatched were lower for Chloroperia tripunctata (Scopoli) (8.5°C, 4.2–17.3°C) than for Siphonoperla torrentium (Pictet) (12.8°C, 6.1–19.4°C). Few eggs hatched at 22.r°C.
3. The relationship between incubation period (d days) and water temperature (T°C) was given by: d=1219/T^1.368 for S. torrentium , d=253/T^0.459 for C. tripunctata . Both equations successfully predicted incubation periods for eggs placed in a stream. The period over which eggs hatched was much longer for C. tripunctata than for S. torrentium at all temperatures.
4. The shorter incubation period (at r>5.6°C) and shorter hatching period for S. torrentium ensure that larvae of this species are already growing when eggs of C. tripunctata start to hatch, but the prolonged hatching period of the latter species ensures a long period of larval recruitment to the population. These differences in egg hatching may reduce competition between the two closely-related species.     

THE BREEDING BIOLOGY OF THE GANNET SULA BASSANA ON THE BASS ROCK, SCOTLAND

The Bass colony is increasing—in 1962 there were 5,350–5,700 breeding pairs; 1,340–1,430 pairs of non-breeders with nests or sites (mainly pairs in their season before first breeding) and 2,000–2,500 “club” birds without nest or site. 15% of nests were occupied by both birds of a pair at the time of the count. Oldest males return to the colony in January, followed by experienced females, considerably later by young adult-plumaged birds, immature birds later still, and the few one year-olds that return usually not until May and June. Mid-cliff sites are the first to be re-colonized each year. Gannets usually breed in their fifth year and there is some evidence that females breed earlier than males. The characteristics of Gannet nests and sites are described. Nests function in raising the egg and young above the morass of the breeding colony, and reach a density of about 2.3 per square metre. Nests are demolished and their positions changed more often than might be suspected. The extremely strong social tendency which causes Gannets to establish their sites amongst or very close to existing breeders probably is the factor ensuring high density and this contributes to synchronization of laying. Egg laying is analysed. Experienced pairs forming an isolated group of 20 nests began laying later and showed less synchronization than two other groups of the same size but from the middle of a dense mass, probably due to the greater social stimulation experienced by the non-isolated groups. The date for first and median eggs was also earlier in larger than smaller groups in the same year. The effect of density as distinct from group size is also discussed. Early eggs are mainly laid on cliff or cliff-edge sites and in large nests. Different groups within the colony produced the median egg within 2–3 days of the end of April each year. In the fullest documented group the mean date was also constant from year to year and closely approached the median, implying a considerable degree of synchronization within the gannetry as a whole. Laying in the observation colony became progressively earlier in successive years, probably due to recovery from previous disturbance. Nevertheless, individual females tended to lay in a fixed position each year with relation to the mean for the group. Increasing age of the female causes earlier egg laying and heavier eggs for up to at least five years. It is suggested that the survival value of seasonally synchronized laying in the Gannet is maximum utilization of a seasonally dependable and abundant food supply for the production of young with the optimal chance of post-fledging survival. The spread of laying acts as an insurance against possible adverse conditions. There is a considerable reserve of unutilized breeding capability within the colony (adult non-breeders, a pre-maturity period longer than physiologically necessary for egg production, and a one-egg clutch when in fact two young can easily be reared). The mean of 393 Gannet eggs was 104.5 gm. (range 81–130). Eggs constitute about 3.4% of adult female weight and lose 9–13% in weight during incubation. Replacement laying of the invariable one-egg clutch takes 6–32 days. The mean incubation period was 43.6 days. Male incubation spells averaged 35.6 hours; female's 32.0 hours. Copulation ceases immediately after egg laying. During three seasons, 82% of eggs laid in the observation colony hatched. Inexperienced pairs hatched 62.6% of eggs laid; experienced pairs hatched 86%. Some of the processes of incubation and chick rearing depend on the maturation of innate abilities and not on experience Inexperienced breeders do not seem inferior to experienced ones in finding enough food for their young. Parental care of the new chick is described; the pterylosis of the chick is figured. A summarized account of plumage development is given. Food fish and chick feeding are described. The average frequency of feeds throughout a continuous two-day watch was 2.7 feeding bouts per chick per day. Adult fishing trips usually took 7–13 hours and the estimated fishing range is over 100 miles, and possibly up to 400 miles, from the breeding colony. Despite this, 15% of daylight hours are spent by the pair together at the nest in addition to the constant guarding of the chick by one or other. Gannet young have a very compressed growth period compared with boobies and fledge at 3,100–4,100 gm., after a steady growth uninterrupted by periods of starvation or arrested development after an average 90 days. 92.3% of all eggs which hatched in 500 nests in the observation colony during three years of the study gave fledged young. Excluding inexperienced birds, there was no difference in the fledging success of eggs laid at different dates in the breeding season, in accordance with the proved abund- ance of food. However, post-fledging survival is probably higher among young fledging at the peak period (first half of September) than later and the few relevant ringing returns tend to support this. Breeding success at the small colony at Bempton was less compared with groups from the Bass for the years 1961–3. Causes of chick loss before and during fledging are discussed. They are unimportant compared with the great mortality in the first year of life after fledging. The adaptive significance of black plumage in the juvenile Gannet probably lies in reduced attack-releasing qualities of such plumage on the male parent. The Gannet alone in the Sulidae produces young which leave the nest with large fat deposits, and which are not fed at all by the parents after fledging. This is possibly another result of adaptation to using a seasonally abundant food supply to the maximum. The present Gannet population increase is discussed in relation to cessation of human predation, the possible impetus given by a temporary but large increase in pelagic fish during the war, but also the overall steady downward trend in fishing returns since the early part of this century. One cannot explain the steady and considerable rise in Gannet numbers only in terms of increased food supply. The fact that, at a time of population expansion and obviously favourable conditions, Gannets are still far from utilizing their full recruiting powers, needs investigating further. It may be partly due to the relative slowness of evolutionary change in a long-lived species with slow population turn-over, if the Gannet has evolved its characteristics in response to an environment different from the present one.     

Variations of hydrogen peroxide and catalase expression in Bombyx eggs during diapause initiation and termination

For diapause eggs of the silkworm, Bombyx mori, diapause initiation is prevented with hydrochloric acid (HCl) at around 20 h post-oviposition while diapause status is terminated with chilling around 5°C. To investigate whether hydrogen peroxide (H(2)O(2)) and catalase expression are involved in diapause initiation and termination, the concentration of H(2)O(2), relatively higher levels of catalase mRNA and activity of catalase were compared between (1) 20-h-old diapause eggs and the HCl-treated diapause eggs, and (2) 10-day-old diapause eggs and the 5°C-chilled diapause eggs. Compared to diapause eggs, the HCl-treated eggs had significantly higher H(2)O(2) concentrations (up from approximately 1-3 μmol/g fresh mass to 5-8 μmol/g fresh mass), higher relative level of catalase mRNA (up from 0 to 35.2%) and higher catalase activity (up from 2.51 units/mg protein to 4.97 units/mg protein) at 96 h post-treatment. On the other hand, the 5°C chilling resulted in significant increases of H(2)O(2) concentration (up from 0.79 μmol/g fresh mass to 5.57 μmol/g fresh mass), relative level of catalase mRNA (up from 0 to 71.4%) and catalase activity (up from 0.88 units/mg protein to 3.42 units/mg protein) within 120 days. The results obtained in this work suggest that variations of H(2)O(2) and catalase expression in Bombyx eggs are involved in diapause initiation and termination.     

ECOLOGY OF THE RED-NECKED FALCON FALCO CHICQUERA IN ZAMBIA

The Red-necked Falcon in southern Zambia is a year-long resident in its breeding territory. The study was conducted on a floodplain and the adjacent acacia savannah in an undisturbed natural environment. The falcon principally nests in natural depressions on frond bases on the leeward side of Borassus Palms but also utilizes old crow and raptor nests. Incubation averaged 33 days and was undertaken by the female. The young fledged after a 36-day nestling period and remained under parental care for up to three weeks after that. Nesting success averaged 1.3 young per nest or 44% of the eggs laid. The post-juvenal moult commenced when the young were five to six months old and continued for six months. Birds comprised 98% of the diet of the falcons. The adults selected larger prey as the nestlings increased in size. The 69-day incubation and nesting period is up to 14 days longer than in similar-sized falcons.     

SOME OBSERVATIONS ON THE DIDRIC CUCKOO

Earlé R. A. 1986. The breeding biology of the South African Cliff Swallow. Ostrich 57: 138–156.

The South African Cliff Swallow Hirundo spilodera breeds in dense colonies usually under man-made concrete bridges. The clutch size is 1–4 eggs but most 4-egg clutches are probably the result of conspecific brood parasitism. The incubation period averages 14,6 days and the fledling period 24,1 days. Although only the female Cliff Swallow has a featherless brood-patch, both males and females incubate effectively. Nestlings reach a maximum weight of up to 31 g between 19 and 22 days, about 10 g more than average adult weights. This weight increase of nestlings is mostly the result of an increase in water content of the body. Both parents feed the chicks, with the highest rate of feeding during the midday hours. In all, 56% of all eggs laid produced flying young, with a recruitment rate of 0,9 young: 1 adult per season.     

The ecology of a Mediterranean tortoise (Testudo hermanni): Reproduction

A three-year study on reproduction in wild populations of Testudo hermanni has shown that:
( a ) sexual activity occurs between March and October, except the nesting season (May and June), and is most frequent in August and September,
( b ) tortoises are promiscuous in their mating habits, there is no evidence of mate selection in relation to size,
( c ) nest site selection is correlated to ground temperature and nesting itself mainly occurs in the early evening before dark, when the ground temperature characteristics are most indicative of a specific site's relative temperature,
( d ) incubation takes about three months and is probably temperature dependent,
( e ) most nests are preyed upon by mammalian predators within a few days after laying (> 90% being destroyed), the main cue being the smell of the eggs,
( f ) average clutch size in Greece is higher than in France, while mean egg weight in France is higher than in Greece, and there is no strong relationship between body size or weight and egg or clutch weight in either country,
( g ) in contrast to other studies, there is no apparent correlation between rainfall and reproduction parameters,
( h ) some females nest in successive years, and more than once in a year, with a laying interval of 10–20 days,
( i ) mean size of sexually active individuals is not significantly different from the mean size of adults, although nesting females are significantly bigger; the minimum size for sexually active males is about 120 mm and for females 130 mm.
The discussion examines these observations in an evolutionary context.     

THE LAYING INTERVAL AND INCUBATION PERIOD OF ROCKHOPPER AND MACARONI PENGUINS

Williams, A. J. 1981. The laying interval and incubation period of Rockhopper and Macaroni Penguins. Ostrich 52: 226–229.

The laying interval and incubation period of Rockhopper Penguins Eudyptes chrysocome and Macaroni Penguins E. chrysolophus were studied at Marion Island in 1974–75 and 1976–77. On average, the laying interval was 4,4 and 4,5 days, the incubation period of second-laid eggs was 34,2 and 35,9 days and that of first-laid eggs was 39,1 and 38,0 days in Rock-hopper and Macaroni Penguins respectively. The laying interval in this genus is longer than that in other penguins. The incubation period is similar to that of most other penguins but the second-laid egg normally hatches before the first-laid egg. The long laying interval and the hatching sequence of the eggs both have important affects upon the mortality of eggs in the genus Eudyptes.     

长江口沿岸碎波带刀鲚仔稚鱼的日龄组成与生长

实验研究了长江口沿岸碎波带刀鲚仔稚鱼的日龄组成、孵化期、早期生长率和滞留时间。从2007年5-10月在长江口沿岸碎波带采集的刀鲚仔稚鱼中,共选取594尾(体长范围为3.0-30.5mm),划分发育阶段,并取矢耳石进行日龄分析。仔稚鱼日龄范围为7-34d,以13-18d日龄比例较高,占总数的50.1%;仔稚鱼体长(L,mm)与日龄(D,days)呈显著直线关系:L=0.73D+5.09,R2=0.74;孵化期为5月23日至10月4日,高峰期集中在5月末至8月上旬,且早期个体在孵化后7d左右开始进入到碎波带,在碎波带滞留约23d。       

黄连木种子小蜂的生物学特性和发生规律

通过田间及室内饲养观察,黄连木种子小蜂EurytomaplotnikoviNikolskaya在河南省太行山区为1年发生1代,以老熟幼虫在被害果内过冬。翌年4月中旬开始化蛹,5月下旬至6月上旬为成虫羽化产卵的盛期。幼虫5月中旬开始孵化,在果内取食至8月中、下旬老熟越冬。成虫在果壳内停留4～5d,出壳后成虫寿命:雄虫3～7d,雌虫4～17d,产卵前期3.7d。平均产卵量35.4粒,卵期3～4d。幼虫共5龄,预蛹期4～5d,蛹期8～10d,蛹期发育过程中形态变化的阶段性分为4级。成虫交尾产卵的最适温度为23～25℃,化蛹、羽化较适宜的湿度为65%～70%。     

Hatching of cladoceran resting eggs: temperature and photoperiod

Summary 1. We identified temperature and photoperiod conditions under which the hatching of 45 cladoceran species could be elicited. Identification of appropriate hatching cues is of primary importance for the exploration of the ties between active and diapausing stages.
2. Incubation temperature affected the hatching success of resting eggs isolated from Danish, Belgian/Dutch and Spanish sediments. In general, most hatchlings and species were retrieved at 15 °C. Danish and Belgian/Dutch resting eggs hatched more successfully under a long day photoperiod than in continuous illumination.
3. Most species could be retrieved after incubation of resting eggs isolated from a limited amount of sediment (0.4 kg) under a single, well chosen combination of temperature and photoperiod. Processing additional sediment samples under seven more incubation regimes only allowed detection of 21% (Spain) to 34% (Denmark) more species.
4. The incubation period for resting eggs to hatch was strongly influenced by incubation temperature. Our results show that hatching experiments aimed at assessing cladoceran species richness and conducted at 15 °C should be continued for a period of at least 2 weeks, after which a random subset of hatchlings (e.g. n  = 100) can be selected from the total hatchling assemblage.