The Early Development of Pygoscelis adeliae (Adélie Penguin) up to the Formation of the Neural Tube

The early embryonic development of Pygoscelis adeliae, up to the stage with fused neutral folds, was investigated by means of serial sections and compared with the development of the chick (Gallus domesticus). The total incubation time in the penguin is about 35 days, compared with about 20 days in the chick (Herbert 1967). This superior rate of development in the chick is likewise recognized in the early period of development; for fusion of neural folds is achieved 45–49 hours after laying in the chick and 6–7 1/2 days incubation in the penguin. Furthermore the time of origin and shape of the neural tube, notochord and heart show recognizable differences in the two genera.     

4. CLIMPSES OF THE NARINA TROGON

Bertram, B. C. R. &; Burger, A. E. 1981. Aspects of incubation in Ostriches. Ostrich 52:36-43.

We studied incubation in domesticated Ostriches Struthio camelus in South Africa and wild Ostriches in Kenya. Although the eggs were large, with relatively high thermal capacities, unattended eggs exposed to the sun reached dangerously high temperatures (40,5°C). Experimental exposure of fresh eggs to the sun for seven days prior to incubation greatly reduced the percentage of embryos which developed, and no embryos survived 15 days of exposure. In the wild. Ostriches frequently shade their eggs in the pre-incubation period to prevent overheating.

During natural incubation, temperatures in the eggs (range 30,8-33,8°C) and of nest-air (31,9-34,6°C) were remarkably constant, despite the daily ambient fluctuations of air temperatures (17,8-38,9°C). Similarly the humidity of the nest-air (39–52%) was lower and less variable than the ambient air (39–72%). Water loss during 42 days of incubation was 11–12% of initial egg weight and, in addition, early laid eggs lost 3–4% during the 2½-3 week pre-incubation period. The water vapour conductivity and the daily water loss of Ostrich eggs were similar to those of other birds, in proportion to epg size, despite the arid environment inhabited by Ostriches. Some of the constraints on the feeding and breeding behaviour of Ostriches imposed by the physical requirements of their eggs are discussed.     

SOME NOTES ON THE SPOTTED FOREST THRUSH

Brown, C. J., Riekert, B. R. &; Morsbach R. J. 1987. The breeding biology of the African Scops owl. Ostrich 58: 58–64.

The incubation and nestling periods of two pairs of African Scops Owls Otus senegalensis breeding in nesting boxes in the Daan Viljoen Game Park near Windhoek were studied. The incubation and nesting periods were about 22 ± 2 days and 25–28 days respectively. Incubation and brooding was by the female. The male provided all the food during the incubation period, but by the end of the nestling period 30% of food was brought by the female. The growth of the nestlings, parental behaviour and foraging methods are describe2 Of 100 food items brought to the nests, 93% (by number) consisted of arthropods, 6% reptiles and 1% small mammals.     

Oviducal development in a Krefft's river turtle,Emydura krefftii gray (Chelonia: Chelidae)

A clutch of Emydura krefftii eggs hatched 20 days after oviposition, in contrast to the normal incubation period of 45–50 days for this species. This shortened incubation and the presence of stage 20–21 embryos at oviposition indicates facultative oviducal development in E krefftii.     

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.     

Artificial incubation of trumpeter swan eggs: Selected factors affecting hatchability

Eggs collected from captive trumpeter swans (Cygnus buccinator) in 1993 (n = 33) and 1994 (n = 42) were artificially incubated with careful monitoring to identify factors contributing to the low hatch success reported by the Ontario Trumpeter Swan Restoration Program. Fertility was > 80% in both years, whereas hatch success of fertile eggs was 14.3% (n = 4) of 28 eggs in 1993 and 37.1% (n = 13) of 35 eggs in 1994. Necropsy of non‐viable eggs indicated a high incidence of embryonic mortality during early and late incubation. Early embryonic mortality was associated with egg storage times exceeding 7 days (P < 0.05) and bacterial contamination of eggs (P < 0.01). Late mortality was associated with (P < 0.001) increased weight loss during incubation period and may have resulted from incubator temperature and humidity fluctuations. We established patterns of weight loss for eggs and determined that hatched eggs lost 11–15% of initial mass and that weight loss >15% resulted in embryo mortality. Results from this study indicate that collection and handling of eggs before incubation and precise control of the incubator environment are critical to hatchability of eggs. Zoo Biol 18:403–414, 1999. © 1999 Wiley‐Liss, Inc.     

NOTES ON BREEDING OF CISTICOLA BRUNNESCENS AND C. JUNCIDIS IN ZAMBIA

Penry, E. H. 1985. Notes on breeding of Cisticola brunnescens and C. juncidis in Zambia. Ostrich 56: 229–235.

Details are given of breeding data from Cisticola juncidis and C. brunnescens in Kitwe. Zambia in December 1979 and January 1980. Composition, structure and dimensions of nests, incubation periods, nestling periods, chick development and breeding success are presented and comparisons are made between the two species for each of these factors. The previously unrecorded incubation period for C. brunnescens is 11–13 days. All published breeding records for the two species in Zambia between 1970 and 1980 have been collated.     

BREEDING BIOLOGY AND BEHAVIOUR OF THE QUAIL FINCH ORTYGOSPIZA ATRICOLUS

Summary

Nuttall, R.J. 1992. Breeding biology and behaviour of the Quail Finch Ortygospiza atricollis. Ostrich 63:110-117.

During a study of the breeding biology of the Quail Finch Ortygospiza atricollis, observations of nest-building, egg-laying, incubation and nestling periods, and nestling development in a grassland near Pietermaritzburg, South Africa were supplemented with observations of breeding behaviour in captivity. Mean clutch size was 4,5 and eggs were laid at intervals of approximately one day. Incubation began after the third or fourth egg was laid. An incubation period of 15–16 days and an estimated nestling period of 18–19 days was recorded. Incubation and brooding are shared by both sexes. Breeding success was low (26,7% ?28,6%), with most losses resulting from predation during either the egg-laying or incubation stages.     

Transmission of rayado fino virus of maize (Zea mays) by Dalbulus tnaidis

Rayado fino virus (RFV) of maize (Zea mays) was transmitted by the leaf-hopper Dalbulus maidis in a manner characteristic of viruses that multiply in their insect vectors. Individual insects fed on infected plants transmitted the virus after incubation periods of 8–22 days; males had shorter incubation periods than females but died sooner. Insects retained infectivity for 1–20 days. Transmission by most insects was intermittent. Inoculativity by D. maidis decreased with time, but the virus was recovered from insects that had lost their ability to transmit. Extracts of plants infected with RFV and viruliferous insects were injected into healthy insects, which became viruli-ferous. Infectivity of the extracts was not affected by tetracycline hydrochloride (Achromycin). D. maidis was able to transmit simultaneously RFV and the corn stunt agent. Other than maize, Teosinte (Euchlaena mexicana) was the only plant susceptible to the virus, among a number of species of Gramineae tested.     

High‐pressure systems for gas‐phase free continuous incubation of enriched marine microbial communities performing anaerobic oxidation of methane

Novel high‐pressure biotechnical systems that were developed and applied for the study of anaerobic oxidation of methane (AOM) are described. The systems, referred to as high‐pressure continuous incubation system (HP‐CI system) and high‐pressure manifold‐incubation system (HP‐MI system), allow for batch, fed‐batch, and continuous gas‐phase free incubation at high concentrations of dissolved methane and were designed to meet specific demands for studying environmental regulation and kinetics as well as for enriching microbial biomass in long‐term incubation. Anoxic medium is saturated with methane in the first technical stage, and the saturated medium is supplied for biomass incubation in the second stage. Methane can be provided in continuous operation up to 20 MPa and the incubation systems can be operated during constant supply of gas‐enriched medium at a hydrostatic pressure up to 45 MPa. To validate the suitability of the high‐pressure systems, we present data from continuous and fed‐batch incubation of highly active samples prepared from microbial mats from the Black Sea collected at a water depth of 213 m. In continuous operation in the HP‐CI system initial methane‐dependent sulfide production was enhanced 10‐ to 15‐fold after increasing the methane partial pressure from near ambient pressure of 0.2 to 10.0 MPa at a hydrostatic pressure of 16.0 MPa in the incubation stage. With a hydraulic retention time of 14 h a stable effluent sulfide concentration was reached within less than 3 days and a continuing increase of the volumetric AOM rate from 1.2 to 1.7 mmol L^?1 day^?1 was observed over 14 days. In fed‐batch incubation the AOM rate increased from 1.5 to 2.7 and 3.6 mmol L^?1 day^?1 when the concentration of aqueous methane was stepwise increased from 5 to 15 mmol L^?1 and 45 mmol L^?1. A methane partial pressure of 6 MPa and a hydrostatic pressure of 12 MPa in manifold fed‐batch incubation in the HP‐MI system yielded a sixfold increase in the volumetric AOM rate. Over subsequent incubation periods AOM rates increased from 0.6 to 1.2 mmol L^?1 day^?1 within 26 days of incubation. No inhibition of biomass activity was observed in all continuous and fed‐batch incubation experiments. The organisms were able to tolerate high sulfide concentrations and extended starvation periods. Biotechnol. Bioeng. 2010; 105: 524–533. © 2009 Wiley Periodicals, Inc.     

Embryological development of Salvator merianae (Squamata: Teiidae)

Here we describe the embryonic development of Salvator merianae external morphologic features, as based on observation of 28 embryos across different days of incubation at 31 ± 0.5°C. Observed developmental stages were grouped and classified into the early, middle, and late periods. The early period (Stages 3–11) is distinguished by the origin of the encephalic vesicles, sensory placodes, pharyngeal arches, and degree of body flexion and rotation. The medium period (Stages 8–15) is distinguished by limb differentiation and by cranium‐facial characteristics. The late period (Stages 15–18) is determined by scale patterns, pigmentation, and embryo growth.     

Daily growth patterns and age‐at‐recruitment of the anchoveta Engraulis ringens as indicated by a multi‐annual analysis of otolith microstructure across developmental stages

The anchoveta (Engraulis ringens ) plays a key role in the ecology of the Humboldt Current System and is of major economic importance; however, many aspects of its early life history are still poorly understood. In this study, an analysis of daily age and length patterns was carried out using the sagittal otoliths from wild larvae (0–0.2 cm standard length, L _S), pre‐recruits (3–6 cm total length, L _T), recruits (7–12 cm L _T) and young adults (12–15 cm L _T). Additionally, variability in growth and age at recruitment (A _R) were evaluated for recruits caught in northern Chile in 1973, 1982, 2009, 2010, 2012, 2013, 2014 and 2015. The age–length relationship showed four allometric patterns that were well described by Laird‐Gompertz models. The absolute growth rates at the inflexion point (G _AR) were 0.56, 0.75, 1.22 and 1.16 mm d^?1 for larvae, pre‐recruits, recruits and young adults, respectively. At the interannual scale, G _AR values were always >1 mm d^?1 (mean ± S.D . 1.37 ± 0.21 mm d^?1; range 1.12–1.64 mm d^?1), irrespective of the season of hatching (i.e. winter v. spring); additionally, in most cases, G _AR values were reached before the second month of life (mean ± S.D . 50.47 ± 9.73 days) at c. 4 cm L _T (mean ± S.D . 4.22 ± 0.29 cm). Mean A _R was < 150 days (112 ± 29 days; range 75–149 days); in contrast, estimates of A _R were higher and growth rates were lower in 1973, 1983 and 2000. These results demonstrate very fast growth and early A _R of anchoveta in northern Chile, suggesting most fish are removed by the fisheries at very early ages. An evaluation of the implications of these results on stock assessment and management of this species is highly recommended.     

The temperature dependence of embryonic and larval development in Protonemura intricata (Plecoptera: Nemouridae)

SUMMARY. 1. Egg development and larval growth of Protonemura intricata (Ris, 1902) (Plecoptera: Nemouridae) were studied in the laboratory and in the Breitenbach, a small stream-in Germany (F.R.G.). 2. The mean number of eggs in batches collected from the field was 627 (S=314). 3. Mean batching success in the laboratory was 60–100% at 2–18°C. Cumulative hatch in individual batches could be described by asymmetrically sigmoid curves. The length of the hatching period was positively correlated with the length of the incubation period. 4. The incubation period of I', intricata normally consists of an initial dormancy followed by subsequent development. The length of embryonic development (Y. days) is strongly inversely temperature (T, °C) dependent and can be described by the equation: 5. The length of dormancy is dependent on oviposition dale, and is shorter the later that the eggs are laid. It also depends on temperature during incubation and is increased by rising temperatures. As a consequence, larvae hatch more or less synchronously in the field during autumn. Total incubation period, i.e. dormancy and actual development, exhibits a complex dependence on both incubation temperature and oviposition date. Under constant laboratory temperatures, a late sharp fall in temperature can terminate dormancy earlier. 6. Photoperiod probably induces dormancy and may already act on the last larval instars of the parent generation. The dormancy of P. intricata is classified as an oligopause (Müller. 1970, 1976). 7. In the laboratory. P. intricata larvae from early batches with long dormancy grew faster than larvae from late batches with direct development. Final size was the same in both cases. This acted against the population synchrony induced through egg dormancy. Benthos samples suggest the same in the field. 8. Avoidance of the suboptimal summer conditions in streams by the cold stenothermous P. intricata is suggested to partly explain the success of the species, which contributes more to total emergence biomass than do other Plecoptera in the Breitenbach.     

Cell Lysis of Cyanobacteria and Its Implications for Nutrient Dynamics

The dynamics of nutrients, such as phosphorus, nitrogen, and carbohydrates, during cyanobacteria cell lysis was investigated under darkness incubation in the laboratory. The cell lysis rate of cyanobacteria sampled from Lake Taihu was measured using an esterase assay. Based on particulate esterase activity, the calculated cyanobacteria lysis rate was 0.094 d^–1. During 30 days of darkness incubation, Chlorophyll a concentration decreased from 56 μg L^–1 to 2.0 μg L^–1. Parallel to this, total particulate carbohydrate concentration decreased rapidly. The fluctuation of dissolved organic carbon concentration was a function of the production of non‐carbohydrate by cyanobacteria and the decomposition of carbohydrate by bacteria. Total dissolved carbohydrates and dissolved polysaccharides concentrations showed a similar pattern, declining at the beginning of the experiment and keeping relatively stable, thereafter. In contrast, the concentration of dissolved monosaccharides remained constant during the entire process. The concentrations of NH₄⁺ and PO₄^3– increased at the early stage, and then decreased afterwards. A gradual decrease in NO₃^– concentration after day 8 indicated that anaerobic conditions might be produced during the cell lysis process. The present results demonstrated cyanobacteria cell lysis has a big influence on the nutrient status of the surrounding water. (© 2010 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim)     

FIELD OBSERVATIONS ON CENTROPUS TOULOU INSULARIS ON ALDABRA ATOLL

Frith, C. B. 1975. Field observations on Centropus toulou insularis on Aldabra Atoll. Ostrich 46:251-257.

Details are presented of the nesting of a pair of Malagasy Coucals on Aldabra, with incidental observations of other pairs and nests. Courtship and copulation behaviour is very similar to that of the black Coucal Centropus grillii of Africa. Both sexes net build and incubate the eggs but these activities are performed very predominately by the male. Eggs are white and average 27,5 x 23.5 mm and 8,3 g. Two complete clutches of two and one of thee egg; were found and a doubtful early record of a four egg clutch is considered unlikely. There was an interval of at least 9 days between the laying of the two egg;, which hatched 7–8 days apart, incubation commencing with the first egg. The incubation of the second egg was 14 days, and the fledging period of both young about 19 days. Nestlings in the chamber produce a snake-like hissing noise, excrete a foul-smelling sticky fluid when handled and burst through the rear chamber wall as means of avoiding predation.

Both members of the pair were in the brown plumage generally considered to be the non-breeding plumage. It is suggested that the plumages of the Aldabran population of Centropus toulou are possibly more complex than previously considered or that the population may be dimorphic.     

Pilot-scale production of mosquitocidal toxins by Bacillus thuringiensis and Lysinibacillus sphaericus under solid-state fermentation

Mosquitocidal toxins of Bacillus thuringiensis israelensis (Bti) and Lysinibacillus sphaericus 14N1 (Ls14N1) were produced under solid-state fermentation using agro-industrial wastes. Sugar beet pulp–sesame meal (1:1) and wheat germ meal–linen meal (1:1) at 9% were the efficient substrate mixtures for the growth and toxin production of Bti and Ls14N1, respectively. Bti was more active after the addition of beef extract (0.2%) or yeast extract (0.5%) to the medium. On the other hand, the addition of yeast extract (0.2%) or NYSM salts (2%) significantly enhanced the toxicity produced by Ls14N1. The optimum conditions for the maximum toxicity of Bti were at pH 7–8, 20–30% moisture, 4–10% inoculum and 7 days incubation. For Ls14N1, the best conditions were pH 6.5–7.5, 20–30% moisture, 4–10% inoculum and 5 days incubation. It was found that the best thickness of carrier-substrates in the plate (15?cm in diameter) for the maximum mosquitocidal activity was about 0.5?cm for Bti and 0.5–1?cm for Ls14N1. Pilot-scale production in aluminium trays applying the above conditions showed a decrement of toxicity of fermented cultures and some plates were contaminated. These problems were dissolved by reducing the moisture content to 15%, increasing inoculum to 10% and manual agitation of trays every-day.     

Columbin inhibits cholesterol uptake in bloodstream forms of Trypanosoma brucei-A possible trypanocidal mechanism

The diterpenoid furanolactone (columbin) from Aristolochia albida inhibited growth of culture forms of Trypanosoma brucei. In vitro analysis of the compound at 5–250 μg/ml showed complete lysis of the parasites within 10–20 minutes post incubation. At 50 μg/ml, columbin killed about 50% of the parasites which initially appeared swollen under phase contrast microscopy. Also the total amount of cholesterol diminished dose-dependently in the presence of 10–100 μg/ml of columbin after a 3-day incubation period.

In vivo analysis of the compound in T. brucei-infected mice revealed that 25 mg/kg administered for 3 consecutive days, completely cleared the parasites from the peripheral circulation. However, columbin could not clear parasites in the cerebrospinal fluid.     

The biology of the Yellowthroated Sandgrouse Pterocles gutturalis in a South African agricultural landscape

Tarboton, W.R., Blane, S. & Lloyd, P. 1999. The biology of the Yellowthroated Sandgrouse Pterocles gutturalis in a South African agricultural landscape. Ostrich 70 (3&4): 214–219.

A local population of Yellowthroated Sandgrouse was monitored from 1988–1992 at Northam, Northern Province, South Africa, a region in which this species was previously an irruptive, non-breeding visitor. Yellowthroated Sandgrouse were found to be year-round residents, foraging and nesting exclusively in areas cleared for agriculture, particularly one-year fallow lands. They ate the dry seeds of a variety of weedy plants, especially Amaranthus and Crotalaria spp. Males outnumbered females 1.35:1. Egg-laying occurred from April-October, with a peak in June. Clutch size (2–3) averaged 2.85 (n=26), and the incubation period for one nest was 26 days after clutch completion. Nesting success was estimated at 24.8% (n=19 nests, 176 nest days), and the daily nest predation rate at 2.55%; predation and ploughing accounted for most nest losses. Average annual productivity was estimated to be within the range 0.42–0.85 young/pair/year. We suggest that the Yellowthroated Sandgrouse depends on the seeds of early successional plants for food and that the recent agricultural development of the region maintains sufficient areas of fallow land to allow this otherwise nomadic species to become a breeding resident.     

Fecundity,nymphal development and longevity of field‐collected tropical bedbugs,Cimex hemipterus

This study examined the fecundity, oviposition, nymphal development and longevity of field‐collected samples of the tropical bedbug, Cimex hemipterus (Fabricius) (Hemiptera: Cimicidae). Under environmental conditions of 26±2°C, 70 ± 5% relative humidity and a 12‐h photoperiod, with bloodmeals provided by a human host, six strains of tropical bedbug had a fecundity of up to 50 eggs per lifetime, over 11–14 oviposition cycles. Increased feeding frequency improved fecundity. After feeding and mating, adult females normally took 2–3 days to produce a first batch of eggs. The oviposition period lasted 2–7 days before cessation of the oviposition cycle. The egg incubation period usually lasted 5–7 days before the emergence of first instars. The nymphs underwent five stadia (the first four of which each took 3–4 days, whereas the last took 4–5 days) before becoming adults at a sex ratio of 1 : 1. More than five bloodmeals were required by the nymphs to ensure a successful moult. Unmated adults lived significantly longer than mated adults (P < 0.05). Unmated females lived up to almost 7 months, but the longevity of mated males and females did not differ significantly (P > 0.05).     

Sporulation,storage and infectivity of obligate aphid pathogen Pandora nouryi grown on novel granules of broomcorn millet and polymer gel

Aims: Producing granular cultures of obligate aphid pathogen Pandora nouryi for improved sporulation and storage. Methods and Results: Small millet–gel granules were made of the mixtures of 80–95% millet powder with 5–20% polymer gel (polyacrylamide, polyacrylate or acrylate‐acrylamide copolymer) and inoculated with mycelia at 30 mg biomass g^?1 dry granules plus 87·5% water, followed by static incubation at 20°C for 4–12 days. The fungus grew well on 12 preparations but best on that including 10% copolymer. An 8‐day culture of this preparation discharged maximally 58·5 × 10⁴ conidia mg^?1 granule at 100% RH and was capable of ejecting conidia at the nonsaturated regimes of 86–97% RH. During storage at 6°C, granular cultures with >85% water content had twofold longevity (120 days) and half‐decline period (34–36 days) of those stored at room temperature. The steadily high water content preserved the cultures better than that decreasing at 6°C. However, conidia from 70‐day‐stored granules were less infective to Myzus persicae nymphs than those from fresh ones based on their LC₅₀s. Conclusions: The millet–gel granules had higher sporulation capacity than reported Pandora cultures and a capability of spore discharge at nonsaturated humidity. Significance and Impact of the Study: The granular cultures are more useful for aphid control.