On the mechanism of air ventilaton in anabantoids (Pisces: Teleostei)

Summary Air ventilation in most Anabantoid species is diphasic, consisting of exhalation and inhalation. Exhalation is the release of air from the accessory breathing organs (suprabranchial chambers) through the mouth either into the water near the surface (e.g.,Ctenopoma) or directly into the atmosphere (e.g.,Osphronemus goramy). Inhalation, i.e., taking in fresh air through the mouth at the surface, immediately follows exhalation. X-ray films show (Figs. 5 and 6) that evacuation of the suprabranchial chambers during exhalation is total or nearly total. This, together with the fact that these chambers can contract at most to a very small extent, led to the conclusion that gas is replaced by water entering the chambers during exhalation and that this water is replaced by fresh air during inhalation. Further analysis of films, including conventional films showing the behavior of the opercular apparatus during air ventilation (Fig. 7), leads to a theory of a double-pumping mechanism responsible for air ventilation. This mechanism consists of the buccal apparatus and the opercular apparatus. It is suggested that both of these structures are able to act as both suction and pressure pumps, and thus air ventilation may be explained as the result of alternating activity of these two pumps.In the monophasic air ventilation characteristic of (adult)Anabas testudineus, there is no exhalation phase comparable to that of other Anabantoids. Therefore, no water enters the suprabranchial chambers, which remain filled with gas during the whole ventilation process (Fig. 10). Ventilation is limited to one phase comparable to inhalation in other Anabantoids.The structure of the accessory breathing organs (Fig. 1) and its progressive complication with growth (Fig. 4) were studied inOsphronemus goramy. The arrangement of the labyrinthine plates is in accordance with the requirements of transport of water and gas through the suprabranchial chambers. One plate (the inner plate, Fig. 1) separates these chambers into atrium, ventro-caudal, and dorso-caudal compartments, each with its own opening (valve). This organization seems essential for the transport of gas and water through the suprabranchial chambers and ensures that during exhalation, water flows into the chambers from above, so that while water is filling these chambers displaced gas can be sucked through the deep-lying pharyngeal openings into the expanding buccal cavity.Supported by the Deutsche Forschungsgemeinschaft     

Effects of temperature on respiration and acid-base balance in a monitor lizard

Summary Ventilation, gas exchange, blood gas tensions and arterial pH were measured simultaneously in monitor lizards,Varanus exanthematicus. In contrast to previously studied poikilotherms, the arterial pH is independent of body temperature within the normally encountered temperature range (Fig. 1). This exception to the relative alkalinity concept (Rahn, 1966) is correlated with the finding thatV. exanthematicus maintains a constant ratio of ventilation to oxygen uptake (and CO₂ production) at different temperatures (Fig. 3). The increase in arterial (Fig. 1) is related to an increase in physiological dead space; i.e., alveolar ventilation increases less with temperature than total ventilation (Fig. 4). This may result from the increased frequency of breathing which results in a reduced breath holding time (Fig. 2). Varanid lizards have a higher oxygen requirement than other reptiles. This is reflected in the control of ventilation, the specialized lung morphology, the high arterial saturation due to low intracardiac shunting, pH regulation and other mammal-like features ofVaranus.     

Respiration of the air breathing fishPiabucina festae

Summary Piabucina festae, a Central American stream fish, breathes air frequently, even in air saturated water, however, is not an obligate air breather. Without access to air, it can maintain routine by aquatic respiration down to aP _wO₂ of about 70 Torr which is its critical O₂ tension (P _cO₂, Fig. 5). Aerial respiration averages 10% of total in air saturated water and 70% in hypoxic water (Fig. 4). At lowP _wO₂ air breathing is more frequent (Fig. 1), and more O₂ is utilized from each air breath (Table 3), and tidal volume may increase (Fig. 7). Vascularized respiratory compartments or cells (Fig. 6), located in the second chamber of the physostomus gas bladder, function for aerial respiration. In ventilation air is gulped and forced through a large pneumatic duct into the gas bladder, excess gas is then released through opercula. Inspiration always precedes expiration and tidal volume is small, keeping gas bladderP _{O 2} low (Table 4). Major differences in the air breathing physiology ofP. festae and other species are its higherP _cO₂, a low aerial in normoxic water, even though air gulps are frequent, and its pattern of inhalation prior to expiration. The interrelationship and optimization of the three gas bladder functions (buoyancy, sound reception, and air breathing) inP. festae is discussed. Aerial respiration may have evolved secondarily to the gas bladder's function in buoyancy control.     

Pineal melatonin rhythms in the lizardAnolis carolinensis: effects of light and temperature cycles

Summary Pineal and ocular melatonin was assessed, over 24 h periods, in male lizards (Anolis carolinensis) entrained to 24 h light-dark (LD) cycles and a constant 32 C, and in lizards entrained to both 24 h LD cycles and 24 h temperature cycles (32 C/20 C). At a constant temperature, the duration of the photoperiod has a profound effect on the duration, amplitude, and phase of the pineal melatonin rhythm (Fig. 1). The pineal melatonin rhythm under cyclic temperature peaks during the cool (20 C) phase of the cycle regardless of whether or not the cool phase occurs during the light or dark phase of a LD 1212 cycle (Fig. 3). Under a temperature cycle and constant dim illumination, a pineal melatonin rhythm is observed which peaks during the cool phase of the temperature cycle, but the amplitude of the rhythm is depressed relative to that observed under LD (Fig. 2). Illumination up to 2 h in duration does not suppress the nocturnal melatonin peak in theAnolis pineal (Fig. 4). No melatonin rhythm was observed in the eyes ofAnolis under either 24 h LD cycles and a constant temperature (Fig. 1), or under simultaneous light and temperature cycles (Fig. 3). Ocular melatonin content was, in all cases, either very low or non-detectable.Abbreviations HIOMT hydroxyindole-O-methyltransferase - NAT N-acetyltransferase     

Sunset-related timing of flight activity in neotropical bats

Summary The times of onset and completion of the hunting flights of three colonies of neotropical bats, each comprising 100–200 individuals, were observed for nine months. The colonies were of different species: Molossus ater (M.a.) and Molossus molossus (M.m.) of the Molossidae, and Myotis nigricans (My. n.) of the Vespertilionidae. Individuals of Phyllostomus hastatus (P.h., Phyllostomidae) were also observed. All the bats roosted in a building near Restrepo, Colombia (4°16N, 73°34W). Times of emergence in the evening and the return of the last animals in the morning were recorded on 2 to 3 successive days each month. For all bats, the emergence time changed in parallel with that of sunset, and the return paralleled sunrise (Fig. 1). Accordingly, the duration of the activity period is positively correlated with the duration of the night. No annual periodic changes in phase (re sunset/sunrise) of the onset and end of flight activity could be demonstrated, but there was a close relationship between the timing of activity and particular light intensities during twilight (Fig. 4). The first flyers of M.a. appear at the highest intensity (30–300 lx) and those of My. n. at the lowest (0.1–5 lx); the last flyers to return appear in the opposite sequence. For each species, the return to the roost usually occurs at a lower intensity than the departure. These findings, made with four neotropical bat species, differ from those of Subbaraj and Chandrashekaran (1977) with the emballonurid bat Taphozous that they studied at 9°58 N in India. The ecological factors that may play a role in timing the flight activity of tropical bats are discussed. Sunset-related timing, based on the combined effect of (a) the circadian oscillation in arousal and (b) the transition during twilight to a light-intensity range with reduced inhibition of activity (lightsampling behavior), tends to be the rule in tropical bats; time-of-day-related timing is the exception.Supported by the Deutsche Forschungsgemeinschaft (Er 59/1-3+6)     

Structure and kinematics of the prosternal organs and their influence on head position in the blowfly Calliphora erythrocephala Meig.

Summary The blowfly Calliphora has a mobile head and various, presumably proprioceptive, sense organs in the neck region. The prosternal organs are a pair of mechanosensory hair fields, each comprising ca. 110 sensilla. We studied their structure (Figs. 2–4), kinematics (Figs. 5, 6) and, after surgery, their influence on head posture (Figs. 7–11) in order to reveal their specific function.The hair sensilla are structurally polarized, all in roughly the same direction, and are stimulated by dorsoventral bending of the hairs (Figs. 3, 4). This occurs indirectly by flap-movements of two contact sclerites (Figs. 3, 6); they move in the same direction during pitch turns of the head, in opposite directions during roll turns, and barely at all during yaw turns of the head (Fig. 5).Bending and arresting all hairs of one field elicits a head roll bias to the non-operated side (Fig. 7) during tethered flight in visually featureless surroundings. In contrast, shaving all hairs of one field elicits a head roll to the operated side (Figs. 8–10). The surgically induced bias of head posture is not compensated within three days (Fig. 10). Our results show that the prosternal organs of Calliphora sense pitch and roll turns of the fly's head, and control at least its roll position.Abbreviations HP° TP° angular positions of the sagittal planes of the fly's head and thorax, respectively, relative to an external reference - HR° = HP — TP head roll angle of the fly's head relative to its thorax, HR>0° for clockwise head roll, looking in flight direction - N number of flies - n number of measurements - PO prosternal organ - SD standard deviation - SEM standard error of the mean     

Spectral mechanisms of the compound eye in the fireflyPhotinus pyralis (Coleoptera: Lampyridae)

Summary Electroretinograms (ERG) were recorded from dark- and chromatic-adapted compound eyes in the dusk-active firefly,Photinus pyralis , at different wavelengths ranging from 320 to 700 run and over 4.5 log units change in stimulus intensity. ERG waveforms differed in the short (near-UV and violet) and long (yellow) wavelengths (Fig. 1). Waveform differences were quantitated by analysis of rise and fall times as a function of the amplitude of the response. Rise times were found to be relatively constant for all stimulus wavelengths. However, variations in the fall times were detected and followed characteristically different functions for short and long wavelengths (Fig. 2).No significant differences in the slopes of the Vlog-I curves at different stimulus wavelengths were observed (Fig. 3).Spectral sensitivity curves obtained from the ventral sector in dark- and chromatic-adapted conditions revealed peaks in the short ( max 400 nm: Fig. 4; max 430 nm: Fig. 5 A; and max 380 nm; Fig. 5B) and long ( max 570 nm: Figs. 4, 5) wavelengths, suggesting the presence of two spectral mechanisms. The long wavelength (yellow) mechanism was in close tune with the species bioluminescence emission spectrum (Fig. 4B).This investigation was supported in part by NIH Research Grant # EY-00490 (to R.M.C.); Research Grant # 01794N from the Research Foundation of the City University of New York (to A.B.L.); NIGMS Training Grant #1 TO 2 GM 05010-01 MARC (to J.A.H.); and NSF Grant # HES-75-09824 (to C.O.T.). We thank Tom Jensen for technical assistance, Barry Schuttler for his courtesy in allowing us to collect fireflies at his farm, Jean Lall for editorial assistance, and the two anonymous referees whose comments added considerably to the quality of this paper.     

Acoustic orientation in adult, female crickets (Gryllus bimaculatus de Geer) after unilateral foreleg amputation in the larva

Summary InGryllus bimaculatus females one foreleg was amputated at the coxa-trochanter joint in the 2nd, 4th or 8th/9th larval instar. A leg of up to normal length is regenerated (Fig. 1) but it lacks a functional ear. In spite of the, usually shorter, regenerated foreleg, the adult one-eared crickets show no impairments in walking when tested on a locomotion compensator. Without sound they walk erratically and most of them weakly circle towards the intact side (Fig. 2).With calling song presentation three response types can be distinguished:tracking (Fig. 3A), hanging on (Fig. 3B) or continuouscircling towards the intact side (Fig. 3C, D). Turning tendencies in monaurals increase with song intensity and exceed those of intact and bilaterally operated animals (Fig. 4). Course deviations towards the intact side also slightly increase with intensity (Fig. 5). Course stability is reduced compared to that of intact animals but exceeds that of bilaterally operated crickets (Figs. 5, 6). It is best at 60 dB and deteriorates at higher sound intensities (Fig. 6). The percentage of monaurals tracking or hanging on decreases with increasing intensity (Fig. 7B). Tracking is established in most animals but it is limited to a narrow intensity range (Fig. 7A, C). Apart from an increased percentage of tracking after early operations (Fig. 7D), there are no prominent changes in orientational parameters with the date of foreleg amputation.Reamputation of the regenerated leg in the adult monaurals does not significantly impair acoustic orientation (Figs. 8, 9), but occlusion of the ipsilateral prothoracic spiracle does (Figs. 10, 11).An attempt is made to correlate the behavioral performance with the activity of auditory interneurons which have undergone morphological and physiological changes (Fig. 12).     

Der Vorderflügel großer Heuschrecken als Luftkrafterzeuger

Summary The mode is demonstrated in which the three regions of the forewings of large grasshoppers, i.e. the costal, radial and anal parts (Fig. 2) are folded against each other during up- and downstroke (Fig. 1; measurements made by W. Zarnack). The aerodynamic effects of this wing folding are determined from the measurements of lift carried out on wing models in parallel air stream (Fig. 3) and on rotating wing models (Fig. 4). Accordingly wing bending during downstroke generates distinctly higher lift at small and medium angles of attack than a flat wing having the same dimensions and moving at the same speed. It generates less lift at high angles of attack. Wing bending during upstroke generates higher lift only at>15°. Lift remains greater than that of a flat wing up to the highest angles of attack. These conclusions are supported by measurements of downstroke wind velocity (Fig. 5). Therefore it is possible to change the lift of right and left wings in order to generate moments for flight control around all three axes of the animal's system of co-ordinates without changing the rough kinematics of the beating wings.

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Der Verfasser dankt Dr. H.K. Pfau für die Einstellung der Flügelmodelle auf typische Mittelpositionen nach funktionsmorphologischen Gesichtspunkten (Abb. 2a) und Dr. W. Zarnack für die Vorpublikationserlaubnis der in Abb. 1 zusammengefaßten Meßdaten. Für meßtechnische Mitarbeit dankt er Frl. cand. rer. nat. U. Britz.     

The release of attack and escape behavior by vibratory stimuli in a wandering spider (Cupiennim salei keys.)

Summary The wandering spiderCupiennius salei responds to vibration of the substrate either with predatory behavior (approach) or with a startle reaction or escape behavior (withdrawal) (Fig. 3). The effects of different parameters of the signal in releasing this behavior were studied by applying various artificial stimuli to a spider standing on a vibrating platform with one or more legs. Receptors sensitive to substrate vibration and the trichobothria, which respond to airborne vibration, together determine the response. Spiders without trichobothria: The type of response to vertical vibrations isfrequency-dependent (Fig. 4a), with predatory reactions predominant at low frequencies (3–4 Hz), and withdrawal reactions at high frequencies (350–460 Hz). Whereas approach is most likely to occur at an intermediate, frequency-dependentamplitude, the probability of withdrawal increases continuously with increasing amplitude (Fig. 6). With sine wave stimuli the lowest threshold amplitude for approach is 9 m peak-to-peak (550 Hz, range tested 1–550 Hz) whereas that for withdrawal is 17 m (800 Hz, range tested 1–800 Hz). The threshold for approach is lower by 6–8 dB whenband-limited noise is used, and the probability of an approach response increases as the bandwidth is expanded. The threshold curve for withdrawal, however, is the same in all cases (Fig. 4b and 5). The spider is capable of both frequency and amplitude discrimination.The metatarsal and pretarsal slit sense organs contribute to these responses as is shown by increased thresholds following their destruction (Fig- 7). Intact animals, with functional trichobothria as well as slit sense organs: They have lower thresholds for withdrawal (by ca. 10 dB; Fig. 9) and shorter reaction times than do spiders without trichobothria. Unlike animals without trichobothria the amplitude thresholds of intact animals to bandlimited noise are ca. 7.5 dB lower than those to sine wave stimuli. The approach threshold is the same as that of spiders without trichobothria. According to direct observation the trichobothria are deflected by airborne sound generated by the substrate motion; the deflection angle increases with both amplitude and frequency of substrate vibration (Fig. 10).There is acentral nervous interaction between the signals from the trichobothria and the slit sense organs with the following basic properties: when both of the two receptor systems receive either a prey-like stimulus or a stimulus eliciting withdrawal their effects add, but when the trichobothria receive stimuli unlike prey they inhibit the approach reaction that would otherwise be triggered by substrate vibration.     

Interspecific variation in temperature dependence of egg development of five congeneric stonefly species (Protonemura Kempny, 1898, Nemouridae,Plecoptera)

Embryonal development of the five congeners Protonemura auberti Illies, 1954, P. hrabei Rauser, 1956, P. meyeri (Pictet, 1841), P. nitida (Stephens, 1835), and P. praecox (Morton, 1894) was studied under various laboratory temperatures and different photoperiods.Mean number of eggs in field collected batches was between 470 (P. praecox) and 1211 (P. auberti). Spring species had smaller egg batches than autumn species (Table 1). Mean hatching success in the laboratory was 50–100% at 2–18 °C. In most species hatching success decreased slightly with increasing temperature (Figs. 1a-e). None of the eggs incubated at 24 °C developed. Hatching pattern followed an asymmetric frequency distribution. In general, the hatching periods were the shorter the higher the incubation temperature.Embryonic development of all five species was inversely temperature dependent (Figs. 2a-e), and well described by a power law relationship (Figs. 3a-e). Interspecific differences in incubation periods were notable at nearly all temperatures (Fig. 4). There was a distinct interspecific sequence in length of incubation period (with steps of about 4 days), which was the same as can be seen in the flight periods: The later the species flies the longer the incubation period. Temperature fluctuations and variations in photoperiod had no influence on incubation and hatching periods or hatching success.The thermal demand of the egg stage neither explains the recent geographical distribution of the Protonemura species, nor does it directly correspond to the field temperatures common during their egg development. However, it is optimal in respect to resource partitioning between the five species, with the consequence of temporal displacement of life cycles.Derived from Brittain's (in press) proposal to compare the two constants a and b of the regressions describing the temperature dependence of embryonal development, a new index (Integral Development Time, IDT) indicating the thermal demand was created for easier comparison of numerous species (Table 2). Evaluation of the IDT for various species of Plecoptera (Fig. 5) suggests that species belonging to the family group Systellognatha generally have higher thermal requirements in the egg stage than species belonging to the Euholognatha.     

Photoreceptor-specific efficiencies of β-carotene,zeaxanthin and lutein for photopigment formation deduced from receptor mutant Drosophila melanogaster

Summary Drosophila rearing media had only -carotene, zeaxanthin or lutein as precursors for photopigment chromophores. Zeaxanthin and lutein are potentially optimum sources of the 3-hydroxylated retinoids of visual and accessory photopigments. Mutants made the electroretinogram in white (w) eyes selective for compound eye photoreceptors R1–6, R7 and R8: R1–6 domiantes w's electroretinogram; R7/8 generates w;ora's (ora = outer rhabdomeres absent); R8 generates w sev;- ora's (sev = sevenless). Microspectrophotometry revealed R1-6's visual pigment. In w, all 3 carotenoids yielded monotonic dose-responses for sensitivity (Fig. 4) or visual pigment (Fig. 7). An ultraviolet sensitivity peak from R1-6's sensitizing pigment was present at high but not low doses (Fig. 1). In w;ora, all 3 carotenoids gave similar spectra dominated by R7's high ultraviolet sensitivity (Fig. 2). For w sev;ora, all spectra were the shape expected for R8, peaking around 510 nm (Fig. 3). The sensitivity dose-response was at its ceiling except for low doses in w;ora (Fig. 5) and zero supplementation in w sev;ora (Fig. 6). Hence, without R1-6, most of our dose range mediated maximal visual pigment formation. In Drosophila, -carotene, zeaxanthin and lutein mediate the formation of all major photopigments in R1-6, R7 and R8.Abbreviations ERG electroretinogram - MSP microspectrophotometry - HPLC high pressure liquid chromatography - n.a. numerical aperture - w, sev, ora Drosophila mutants - y, p, r marg types of R7 and R8     

Frequency response characteristics of electroreceptors in weakly electric fish (Gymnotoidei) with a pulse discharge

Summary Three species of Gymnotid fish, two species ofHypopomus andRhamphichthys rostratus, each having pulse type electric organ discharges (EOD) of different durations were studied to learn if any correlation exists between the spectral composition of the species specific EOD pulse and the frequency response characteristics of that species' electroreceptors. The receptor population consisted of two major categories (examples in Fig. 3). One category, termed pulse marker receptors, responded to suprathreshold stimulus pulses with a single spike at a short (<2 ms) latency. These receptors were tuned to the higher frequency components of a species' EOD (Fig. 4A) and were always 5 to 10 dB less sensitive than any other electroreceptors within a given species. The second major receptor category, burst duration coders, responded to an electrical stimulus with a burst of spikes at a longer latency, burst length was a function of stimulus amplitude. This second category could be further divided into three sub-categories according to the receptors' frequency response characteristics. The most commonly seen subcategory, wide band receptors (Fig. 4B), responded best to stimuli having frequencies equal to the dominant frequency component of the species' EOD in the two species ofHypopomus studied. A second subcategory, narrow band receptors (Fig. 4 A), had frequency response characteristics similar to those of the pulse marker receptors; however, these had thresholds 10 dB lower than those of the pulse marker. The third subcategory of burst duration coders, low frequency receptors (Fig. 4 C, D), responded best to stimulus frequencies ranging from about 50 to 150 Hz. Mechanisms of coding stimulus amplitude and responses to prolonged sinusoidal electrical stimuli were also studied in the various receptor types.It is suggested that the differences in the major receptor types and the different frequency response characteristics of the electroreceptors within a given species allows the animals to identify and evaluate signals resulting from their own EOD, the EODs of conspecifics and electrical stimuli generated by other species of electric fish.Supported by NIH Grant #1 RO1 NS 12337-01     

Ionic bases of action potentials in identified flatworm neurones

Summary The ionic bases for generation of action potentials in three types of identified multimodal neurones of the brain ofNotoplana acticola, a polyclad flatworm, were studied. The action potentials were generated spontaneously, in response to water-borne vibrations, or by intracellularly injected current pulses. At least three components comprise the depolarizing excitable phase of the action potentials: (a) a rapidly inactivating TTXsensitive Na⁺ component (Fig. 2); (b) a Ca⁺⁺ component that is unmasked by intracellular TEA⁺ (Figs. 4, 6, 7); (c) a TTX-resistant Na⁺ component (Fig. 8). Two K⁺ currents appear to account for the repolarization phase of the action potentials: (a) a rapid K⁺ current that is blocked by intracellular TEA⁺ (Figs. 4, 7, 8) and (b) a Ca⁺⁺ -activated K⁺ conductance that is blocked by Ca⁺⁺ and Ba⁺⁺ (Fig. 6). Ionic mechanisms in the generation of action potentials in the central multimodal neurones ofNotoplana pharmacologically resemble those in higher metazoans.Abbreviations TTX tetrodotoxin - TEA ⁺ tetraethylammonium ion - LY lucifer yellow - HRP horseradish peroxidase - BRA bilaterally reciprocally arrayed neurons - SC single contralaterally projecting - SIC single ipsilaterally and contralaterally projecting neurons - HAP hyperpolarizing after potential - AHP after hyperpolarization - EGTA ethyleneglycol-bis-(-amino-ethyl ester) N,N-tetra-acetic acid     

Nist?kologische Sonderung mitteleurop?ischer Fringillidenarten im Biotop Streuobstwiese

Zusammenfassung Kernbeißer brüteten früh und verließen das Untersuchungsgebiet nach der ersten Brut. Ebenfalls früh brüteten Buchfink, Grünfink, Hänfling und Girlitz. Der Stieglitz begann in allen Jahren später mit der Brut als die übrigen Arten (Abb. 2). Die Brutperiode beim Stieglitz war stark verlängert. An den Neststandorten wurden je neun Merkmale erfaßt. Dabei ergaben sich interspezifisch statistisch sicherbare Unterschiede in der Nesthöhe (Tab. 2), der Höhe der Nestbäume (Abb. 3), Entfernung von der Stammitte (Tab. 3), Entfernung der Nester von der Peripherie der Bäume (Abb. 4), Abstand von der Stammitte bis zur Peripherie der Bäume, Stärke der Nesttragäste (Abb. 5), Exposition der Nester (Abb. 6), Lichtmenge am Neststandort (Abb. 7) und bei der Auswahl der Baumarten (Tab. 5). Mit der Zunahme der Höhen- und Breitenausdehnung der von den Vögeln ausgesuchten Nistbäume wurden die Nester entsprechend höher und weiter von der Stammitte entfernt angelegt. Mit zunehmender Astdicke, die die Vogelarten als Nestunterlage wählten, nahm der Abstand der Nester von der Peripherie zu (Abb. 8). Die Neststandorte der Arten ließen sich in einzelne Baumbereiche einordnen. Dabei ergab sich folgendes Verteilungsmuster (Abb. 11): Im innersten Baumbereich brüteten Buchfink und Kernbeißer, wobei letzterer nur die Sonnenseite der Bäume nutzte. Im mittleren Bereich und teilweise auch in den weiter peripher gelegenen Bereichen fanden sich die Grünfinkennester. Daran schlossen sich nach außen die Neststandorte der Girlitze an. In den periphersten Bereichen fanden sich die Stieglitze. Hänflinge brüteten in niedriger Vegetation.

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Nest-habitat separation of six European finch species in orchards

Summary The habitats of finches (HawfinchCoccothraustes coccothraustes, GoldfinchCarduelis carduelis, GreenfinchChloris chloris, LinnetAcanthis cannahina, SerinSerinus serinus and ChaffinchFringilla coelebs) are described, together with the number of nests of birds and periods of time spent in the breeding grounds (Fig. 2), orchards (Fig. 1) on the Limburg (48°36N/9°38E). The breeding seasons of the species differed (Fig. 2). Hawfinches began early in the year with breeding and left the study area after the first brood. Chaffinch, Greenfinch, Linnet and Serin also bred early, whereas Goldfinches were the latest of all species and the span of their breeding season was prolonged. This can be regarded as an adaption or compensation of the influence of predators on the nesting success. At each nesting place found (396 in total, see Table 1) 9 different measurements were made. Between the species there were statistically significant differences with regard to the following features: The height of the nests above the ground (Table 2), the height of the nesting trees (Fig. 3), the distance from the trunk to the nests (Table 3), the distance from the nests to the periphery (Fig. 4), the length of the nesting branch, the thickness of the branch at the location of the nest (Fig. 5), the compass direction of the nests (Fig. 6), light influx (Fig. 7) and the tree species (Table 5). Factor-, discriminant- and cluster-analysis revealed: The higher and the broader the nesting trees were, the higher the nests were placed and the greater was the distance from the centre of the trees. The thicker the branches at the nesting site, the farther was the distance to the periphery (Fig. 8). The nest sites of the species investigated were located at different parts of the tree (Fig. 10). In the innermost part near the trunk the nests of Chaffinch and Hawfinch were found, the latter placed its nests towards the sunny side of the tree (Fig. 6). Greenfinches constructed their nests in the middle part of the tree, whereas Serins tended to build their nests in the more peripherial region, and Goldfinches mainly used the most peripherial regions for nesting. Linnets bred in lower vegetation. The nesting-habitats were discussed and could be interpreted as a niche separation between the species.

     

Zur Glykolatoxydation einzelliger Grünalgen

Summary O₂-uptake and CO₂-release by a chlorophyll-free, carotenoid-containing mutant of Chlorella vulgaris increase on addition of Na-glycolate by factors of 4–5 and 5–6, respectively (Fig. 1). In an enzyme preparation of that alga (sonification, centrifugation, precipitation with 0–30% (NH₄)₂SO₄, dialysis) activity of glycolate oxidase can be demonstrated by O₂-uptake (Fig. 2a) as well as by reduction of the artificial electron acceptor DCPIP (Fig. 2b). The same holds true for whole cells as well as equally prepared enzyme preparations of heterotrophically or autotrophically grown wildtype Chlorella vulgaris, provided the cells are cracked by a French press instead of a sonicator (Figs. 3a-c and 4a-c). Glyoxylate is the main reaction product (Table). Oxidation of exogenous glycolate is rapidly performed by whole cells of Scenedesmus quadricauda and of Ankistrodesmus convolutus, too, but hardly or not at all by Chlorella pyrenoidosa and Ankistrodesmus braunii. No definite influence of the level of CO₂ applied during growth is found: Chlorella vulgaris and Ankistrodesmus convolutus show a rapid oxidation of glycolate after growth under 0,03 and 1,5% CO₂ in air, whereas Chlorella pyrenoidosa and Ankistrodesmus braunii do not show an enhanced O₂-uptake on addition of glycolate after either condition (Fig. 5). Various developmental stages of Chlorella pyrenoidosa respond differently to addition of glycolate, the extra O₂-consumption varying between about 25% (mature cells) and 50–60% (young cells) of the endogenous rate (Fig. 6). It thus appears that species of unicellular green algae within the same genus have strong or weak glycolate oxidase activity and that several external factors have only a modifying effect on that enzyme.     

Lampenbürstenchromosomen in den Oocytenkernen von Sepia officinalis

The nuclei of the growing oocytes of Sepia officinalis contain lamp-brush chromosomes with clearly demonstrable chromomeres bearing pairs of lateral loops (Fig. 4). Similar to the findings of Callan and Lloyd (1960) in amphibian oocytes the chromosomes of Sepia exhibit some specially organized loops which can be used as landmarkers for recognizing certain chromosomes (Fig. 5). Maximal loop despiralization occurs only in nuclei of follicles during their initial growth phase. The following developmental period is characterized by a successive contraction of loops and chromosome axes (Fig. 7), despite the fact that the diameter of the oocyte nucleus enlarges still three times. In the oldest nuclei hundreds of nucleolus-like granules arise near the chromosomes which later spread over the entire nucleus (Fig. 9).

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Herrn Professor Dr. K. Bier () in dankbarer Verehrung gewidmet.     

The physiology of exercise at and above maximal aerobic capacity in a theraphosid (tarantula) spider,Brachypelma smithi (F.O. Pickard-Cambridge)

Summary The physiology of activity in a large (ca. 30 g) mygalomorph (‘tarantula’) spiderBrachypelma smithi, was investigated for 10 min runs at speeds of 2.0, 2.5, and 5.0 cm/s. No differences in were observed at the different speeds suggesting that maximum steady-state aerobic metabolism was achieved. These, levels were eight times greater than those measured in resting spiders and in agreement with predictions based on estimates of the functional capacity of their book lungs (Table 3). Heart rates increased from 18 to 58 beats/min during activity (Fig. 4) while ventilation rates increased from 10/h to 114/h (Table 2). Changes in heart rates indicate, systemic hemolymph perfusion is maintained during activity in contradiction to reports suggesting circulation is compromised by fluid pressures generated during hydraulic leg extension in these animals. Hemolymphd-lactate concentrations increased ca. nine fold during running at 5 cm/s from a resting concentration of 1.7 mM. Peak values occurred from one to two h after the end of exercise (Fig. 5). Anaerobic contributions during exercise, via lactate production, accounted for no more than 30% of the total ∼P synthesized (Table 4). Lactate removal was slow: four h after activity, concentrations in the hemolymph remained ca. 8.5 mM (Fig. 5). Maximum in spiders are much lower than those in active insects, a difference that reflects the effectiveness of tracheal gas exchange of insects compared with respiratory gas transport book lungs and an open circulatory system found in spiders (Table 5). Direct measurements of body temperatures indicate theraphosids are not endothermic during activity.