The postcranial skeleton of Kingoria nowacki (von Huene) (Therapsida: Dicynodontia)

A new specimen of Kingoria nowacki (von Huene) with a complete pelvic girdle and hindlimb is reconstructed and the method of locomotion analysed. It is concluded that the hindlimb was modified from the normal dicynodont pattern in a direction comparable to that of advanced mammal-like reptiles which are presumed to have given rise to mammals. The pectoral girdle also had a modified form, but the humerus was probably conservative in its morphology. The hindlimb stride relied on protraction and retraction to effect movement while the forelimb relied on long axis rotation of the humerus. Possible reasons for the difference in morphology and function of the fore-and hindlimbs are discussed, and a functional sequence for the generation of the Kingoria pelvic girdle from that of other Permian dicynodonts is suggested.     

Growth and yield of six short varieties of spring wheat derived from Norin 10 and of two European varieties

Five short varieties of spring wheat derived from Norin 10: Lerma Rojo 64A (R), Penjamo 62 (P), Sonora 64 (S), Mexico 120 (M), and an unnamed selection obtained from Mexico (X), had grain yields equal to, or only slightly less than those of the taller European spring varieties Kloka (K) and Jufy I (J). Yields ranged from 500 to 580 g/m² of dry matter. The short variety NBJ115 (N) was severely infected with yellow rust and yielded only 290 g/m². Total dry weight (excluding roots) of the short varieties was less than of J and K; hence grain accounted for 49 % of the total for the short varieties and 42 % for J and K. Most of the short varieties had fewer ears than the tall ones because sowing difficulties and poor germination produced fewer plants. The relative yields of X, P, R and S seemed to be correlated with their plant and ear densities. Leaf area duration after flowering (D), based either on total green area or on green area above the flag-leaf node only, was less for the short varieties than for J and K. The apparent mean efficiency of this area in grain production (grain yield divided by D) was 50% greater for the short than for the tall varieties. The height of the short varieties ranged from 43 cm (M) to 79 cm (N). K was 92 cm and J 97 cm tall. Differences in height depended on the lengths of the top four internodes and not on number of internodes. Main shoots of all varieties produced seven or eight leaves. All varieties initiated spikelets 45–48 days after sowing. The short varieties flowered 103 days and matured 155 days after sowing; J and K flowered and matured about 1 week earlier.     

The Abundance of Different Peritrich Ciliates on Stone Surfaces in Contrasting Lowland Streams Throughout the Year

ABSTRACT. Pentrich ciliates attached to small stones from the beds of two streams, one large with hard water, the other small with soft water, were enumerated throughout an annual cycle. Throughout the year, Platycola was the dominant peritrich in both streams, except for a brief period during the spring when Vorticella and Carchesium predominated. Vorticella reached peak levels of 89 ciliates cm² of stone surface, and up to 102 Platycola per cm² of stone surface were found. Mean volumes of samples of the main species were calculated, and used to estimate the standing stock biomasses. using a standard value of dry weight per unit volume. Published values of the growth rates of representatives of the main genera were used to estimate production values, which totalled about 6.5 g dry weight of peritrich cytoplasm/m² of stream bed per annum in the large stream (mean annual density = 8.3 peritrichs/cm² of stone surface), and 33 g dry weight/m² of stream bed per annum in the small stream (mean annual density = 47 peritrichs/cm² of stone surface). Food supply, temperature and predation were the primary factors determining peritrich abundance     

Effects of variation in ear temperature on growth and yield of spring wheat

Wheat plants were kept in a growth room at 15 ^oC from 7 days after an-thesis until maturity and their ears were warmed to 20 or 25 ^oC for various periods. Continuous warming initially increased the growth rate of the ear and decreased that of the stem, but hastened senescence of the ear and decreased final grain yield by decreasing dry weight per grain. Warming the ears increased the movement of ¹⁴C and nitrogen to them from the leaves and stem during the early stages of grain growth but decreased it later. Warming the ears for only the first 10 or 20 days also hastened ear senescence; grain yield decreased progressively with increase in duration of the warm period. All effects were greater at 25 than at 20 ^oC. The effects of changing ear temperature from 15 to 20 ^oC were independent of the temperature of the rest of the plant. Altering the humidity of the air around the ears by 4–7 mb at constant temperature had no effect on ear growth or senescence. Warming all of the plant except the ears from 15 to 20 ^oC increased ear growth slightly during early grain growth and decreased it later, irrespective of ear temperature: stem dry weight, leaf area and net photosynthetic rate of flag leaves and green stems were decreased and dark respiration rate of stems was increased.     

Distribution of Dry Matter between Ear and Shoot of Plumage Archer and Proctor Barley grown in the Field

In a field experiment where Proctor barley yielded slightlymore grain than Plumage Archer but had similar total dry weight,the dry-weight ratio of ear to shoot was greater for PlumageArcher than for Proctor at ear emergence and greater for Proctorat maturity, as in a previous pot experiment. When ears wereshaded, the ear: shoot dry-weight ratio at maturity of Proctorwas not significantly greater than that of Plumage Archer. Thevarietal difference in ear: shoot ratio was reversed becauseears of Proctor had a greater relative growth-rate than earsof Plumage Archer, apparently because they photosynthesizedmore. Proctor shoots decreased in weight slightly less thanshoots of Plumage Archer.     

Growth of Hyphal Branching Systems in Coprinus disseminatus

Apical portions of hyphal branching systems of Coprinus disseminatuswere observed at the margins of colonies extending at a constantrate under one set of environmental conditions. Growth was consistentlymonopodial, the main hyphae continuing to extend in the colonymargin at a constant rate. Primary branch initiation occurredat regular intervals, closely associated with cell divisionof the parent hypha, and initiation of secondary branches tookplace in the older parts of the system. Extension rates of main,primary branch, and secondary branch hyphae were distinct, beingin the proportions 100: 66: 18. In the majority of systems successivebranches of the same category closely resembled one anotherand changes in extension rate of primary branches were smallfrom soon after initiation up to a length of 750µ. Ina minority of systems branch behaviour was less regular, somebranches increasing in extension rate whilst others decreased.Changes in older parts of the systems were not followed. young primary branch hyphae were consistently narrower thanmain hyphae. Although extension rate was correlated with hyphaldiameter for main and for branch hyphae separately, the extensionrate of equally wide hyphae was significantly higher for mainas compared with branch hyphae. Furthermore the wider, faster-extendingbranch hyphse temded tp arise from the wider, faster-extendingmain hyphae. The significance of these findings is discussed.     

Photosynthesis of Ears and Flag Leaves of Wheat and Barley

Immediately after anthesis ears of spring wheat absorbed lessthan 0.5 mg CO₂, per hour in daylight and later evolved CO₂,in the light and in the dark. The rate of apparent photosynthesisof the combined flag-leaf lamina and sheath and peduncle (collectivelycalled flag leaf) of two spring wheat varieties, Atle and JufyI, was 3–4 mg per hour; the rates of the flag leaf andthe ear of two spring barleys, Plumage Archer and Proctor, wereeach about 1 mg per hour. The gas exchange of ears and flag leaves between ear emergenceand maturity accounted for most of the final grain dry weight.The CO₂, fixed by the wheat ear was equivalent to between 17and 30 per cent of the grain weight, but more than this waslost by respiration, so assimilation in the flag leaf was equivalentto 110–20 per cent of the final grain weight. In barley,photosynthesis in the flag leaf and the net CO₂ uptake by theear each provided about half of the carbohydrate in the grain. Barley ears photosynthesized more than wheat ears because oftheir greater surface, and flag leaves of wheat photosynthesizedmore than those of barley because they had more surface anda slightly greater rate of photosynthesis per dm².     

Vicars,tramps and assembly of the New Zealand avifauna: a review of molecular phylogenetic evidence

The avifauna of New Zealand is taxonomically and ecologically distinctive, as is typical of island biotas. However, the potential for an old geological age of New Zealand has encouraged a popular notion of a ‘Moa’s ark’ based on the idea that much of the fauna was isolated when Zealandia broke from Gondwana c. 83 million years ago. Molecular phylogenetics has proved useful for exploring the relative importance of different biogeographical processes, revealing for example that ‘tramp’ species (widely dispersing taxa) have arrived in New Zealand even in the last few hundred years, and that some avian taxa have close phylogenetic relatives overseas (predominantly Australian), indicating their recent ancestors were tramps, too. Distinctive taxa with deep phylogenetic ancestry might be ‘vicars’ that owe their presence to vicariance, but lack of close morphological, taxonomic and phylogenetic affinity provides only tenuous evidence for this. Disproving the alternative possibility that apparent vicars are descended from tramps that dispersed in earlier times remains challenging, but molecular analyses have yielded startling insights. Among New Zealand’s iconic taxa, the world’s largest eagle shared a Pleistocene ancestor with a small Australian eagle, and giant, flightless moa are phylogenetic sisters of the much smaller, flying tinamous of South America. The New Zealand avifauna is neither isolated nor stable, but demonstrative of prolonged and ongoing colonization, speciation and extinction.