scholarly journals Diversity and population densities of coraciiform birds in Zambezi riparian forest

2019 ◽  
pp. 179-186
Author(s):  
Kopij G.

A territory mapping method was used in 2015 to assess the population density of coraciiform species breeding in a riparian forest on the Zambezi River near Katima Mulilo, NE Namibia. The forest, c. 280 ha in surface area, was partly transformed by human settlement and arable grounds. A total of 13 species and 42 breeding pairs were recorded. Population densities were (pairs/100 ha) as follows: grey–headed kingfisher 4.3; giant, pied and woodland kingfisher, each one with 1.1; malachite kingfisher 0.7; striped kingfisher 0.4; white–fronted bee–eater 1.4; little bee–eater 1.1; lilac–breasted roller 0.7; broad–billed roller 1.1; African hoopoe 0.7; red–billed wood–hoopoe 1.1; and scimitar–billed wood–hoopoe 0.4. Data published through GBIF (Doi: 10.15470/s9rlud).

2019 ◽  
Vol 5 (4) ◽  
pp. 5-11
Author(s):  
Grzegorz Kopij

A territory mapping method has been employed in 2015 to assess the population density of 8 non-passerine and 10 passerine uncommon bird species breeding in a peri-urban riparian forest (280 ha) along Zambezi River (7 km long) near Katima Mulilo NE Namibia. The population densities (pairs per 100 ha) are estimated as follows: Trumpeter Hornbill: 1.4, Schalow’s Turaco: 2.9, Green-backer Heron: 1.1, Little Bittern: 0.4, Lesser Jacana: 0.4, African Finfoot: 0.4, White-crowned Lapwing: 0.7, Long-billed Crombec: 3.9, Yellow White-eye: 4.3, Scarlet-chested Sunbird: 0.7, African Golden Oriole: 2.9, Black-headed Oriole: 0.7, Violet-backed Starling: 0.7, Pied Wagtail: 8.6, Ashy Flycatcher: 0.4, Black Flycatcher: 0.4, Hartlaub’s Babbler: 4.3.


1992 ◽  
Vol 70 (10) ◽  
pp. 2005-2008 ◽  
Author(s):  
Robert Hall ◽  
Lana Gay Phillips

Evidence is presented that population dynamics of Fusarium solani f.sp. phaseoli in soil depend on the effects of crop sequence and rainfall on parasitic activities of the pathogen. In a rotation trial started in 1978 and conducted over 14 years, population densities (colony-forming units/g) of the fungus in soil remained below 50 in treatments (fallow, repeated corn, repeated soybean) where the preferred host plant (common bean, Phaseolus vulgaris) was not grown. Where bean was grown every 3rd year or every year, population densities reached 475 and 660, respectively, by 1984. Thereafter, population densities of the fungus fluctuated widely from year to year in both rotation and repeated bean treatments. In the rotation treatment, peaks in population density of the pathogen coincided with the years of bean production. In repeated bean plots between 1985 and 1991, population density of the fungus in June was significantly correlated (r = 0.77, p = 0.04) with total rainfall received during the previous summer (June–August). It is postulated that higher rainfall during the growing season of the bean crop stimulated root growth and root infection, leading to the accumulation of higher levels of potential inoculum in infected tissue and the release of higher levels of inoculum into the soil by the following June. Key words: Fusarium solani f.sp. phaseoli, bean, Phaseolus vulgaris, rainfall, crop rotation.


2000 ◽  
Author(s):  
G. M. H. Laheij ◽  
B. J. M. Ale ◽  
J. G. Post

Abstract In the Netherlands, the individual risk and societal risk are used in efforts to reduce the number of people exposed to the effect of an accident at an establishment with dangerous substances. To facilitate the societal risk planning policy an investigation was carried out for the Dutch SEVESO establishments to investigate the possibility of determining a generic uniform population density for the zone between the individual risk contours of 10−5 and 10−6 per year. The indicative limit for the societal risk at this density was not to be exceeded. Also there was to be enough space left for a significantly higher population density outside the individual risk contour of 10−6 per year. The RORISC methodology and the actual data for the 124 Dutch SEVESO establishments were used to determine the generic uniform population density. Based on the data available it can be concluded that the maximum allowed uniform population density in the zone between the individual risk contours of 10−5 and 10−6 per year is lower than one person per hectare. At this density there is no space left for a higher population density outside the individual risk contour of 10−6 per year. For uniform population densities the relative contribution to the societal risk has been found significant up to the individual risk contour of 10−7 per year.


Author(s):  
Keigo Minami ◽  
Ricardo Victoria Fº

An experiment was carried out to study the effects of the following population densities cauliflowers (plants per ha): 20,833 (0.60 m x 0.80 m), 25,641 (0.60 m x 0.65 m), ....37.037 (0.60 m x 0.45 m) , 55.555 (.0.60 m x 0.30 m), and 111,111 (0,60 m x 0,15 m) ; variety Snow ball. It was concluded that the effects of plant population density are greater on curd quality (weight and size) than on production per ha. The best plant population density to produce cauliflowers curd for Brazil market is from 20,000 to 25,000 plants/ha while for mini-curd is above 55,000 plants/ha.


1977 ◽  
Vol 28 (4) ◽  
pp. 417 ◽  
Author(s):  
R Marchant ◽  
WD Williams

Quantitative samples of P. zietziana were taken monthly for two years from Pink Lake and Lake Cundare. Shrimps were usually contagiously distributed. To reduce error, samples were stratified resulting in confidence limits of 40-50% for the mean population density. Despite this variability, stable trends emerged, and variation was not so great as to mask significant differences. Length-frequency analyses distinguished cohorts; a regression was established between length and dry weight, enabling growth to be estimated from samples. By combining growth with population densities in Allen curves, production was computed. In Pink Lake and Lake Cundare mean pro- duction was 11.3 and 1.0 g dry weight m-2 year-1 respectively. Generally there were two or three generations per year, but time and extent of recruitment were not predictable. Each generation suffered continuous mortality, the death of young shrimps accounting for most of the production. This mortality remains unexplained; there are no significant predators and salinity and temperature stress would occur only during summer.


2021 ◽  
Author(s):  
Vince Ndou ◽  
Edmore Gasura ◽  
Pauline Chivenge ◽  
John Derera

Abstract Development of ideal breeding and crop management strategies that can improve maize grain yield under tropical environments is crucial. In the temperate regions, such yield improvements were achieved through use of genotypes that adapt high plant population density stress. However, tropical germplasm has poor tolerance to high plant population density stress, and thus it should be improved by temperate maize. The aim of this study was to estimate the genetic gains and identify traits associated with such gains in stable and high yielding temperate x tropical hybrids under low and high plant population densities. A total of 200 hybrids derived from a line x tester mating design of tropical x temperate germplasm were developed. These hybrids were evaluated for grain yield and allied traits under varied plant population densities. High yielding and stable hybrids, such as 15XH214, 15XH215 and 15XH121 were resistant to lodging and had higher number of leaves above the cob. The high genetic gains of 26% and desirable stress tolerance indices of these hybrids made them better performers over check hybrids under high plant population density. At high plant population density yield was correlated to stem lodging and number of leaves above the cob. Future gains in grain yield of these hybrids derived from temperate x tropical maize germplasm can be achieved by exploiting indirect selection for resistance to stem lodging and increased number of leaves above the cob under high plant density conditions.


1952 ◽  
Vol 3 (1) ◽  
pp. 32 ◽  
Author(s):  
AMR Burnet

Experimental trapping of eels, using carrion-baited traps, was carried out on a number of rivers of various types throughout New Zealand. Where possible, a mathematical analysis has been applied to the trapping results and an estimate of the efficiency obtained. Total trappable population densities of between 30 and 1,368 lb./ac. Were found. An attempt has been made to correlate type of river with the population density. The amount of cover present is apparently the limiting factor. The baited trap takes very few eels of less than 24 in. long and is thus not a very efficient means of keeping a stream free from eels. The feeding habits of the eel are generalized and readily adaptable to most faunas. In most rivers trout occurred only infrequently in the stomach contents.


Land ◽  
2018 ◽  
Vol 7 (4) ◽  
pp. 136 ◽  
Author(s):  
Caitlin Cunningham ◽  
Karen Beazley

Biodiversity hotspots are rich in endemic species and threatened by anthropogenic influences and, thus, considered priorities for conservation. In this study, conservation achievements in 36 global biodiversity hotspots (25 identified in 1988, 10 added in 2011, and one in 2016) were evaluated in relation to changes in human population density and protected area coverage between 1995 and 2015. Population densities were compared against 1995 global averages, and percentages of protected area coverage were compared against area-based targets outlined in Aichi target 11 of the Convention on Biological Diversity (17% by 2020) and calls for half Earth (50%). The two factors (average population density and percent protected area coverage) for each hotspot were then plotted to evaluate relative levels of threat to biodiversity conservation. Average population densities in biodiversity hotspots increased by 36% over the 20-year period, and were double the global average. The protected area target of 17% is achieved in 19 of the 36 hotspots; the 17 hotspots where this target has not been met are economically disadvantaged areas as defined by Gross Domestic Product. In 2015, there are seven fewer hotspots (22 in 1995; 15 in 2015) in the highest threat category (i.e., population density exceeding global average, and protected area coverage less than 17%). In the lowest threat category (i.e., population density below the global average, and a protected area coverage of 17% or more), there are two additional hotspots in 2015 as compared to 1995, attributable to gains in protected area. Only two hotspots achieve a target of 50% protection. Although conservation progress has been made in most global biodiversity hotspots, additional efforts are needed to slow and/or reduce population density and achieve protected area targets. Such conservation efforts are likely to require more coordinated and collaborative initiatives, attention to biodiversity objectives beyond protected areas, and support from the global community.


1988 ◽  
Vol 28 (1) ◽  
pp. 99 ◽  
Author(s):  
MJ Blumenthal ◽  
VP Quach ◽  
PGE Searle

The effect of soybean population density on soybean yield, nitrogen accumulation and residual nitrogen was examined at Camden, N.S.W. (34�S.). In the first experiment, treatments were soybeans (cv. Ransom) at 50, 100, 200 and 400 x 103 plants ha-1; maize (cv. XL66); and a weed-free fallow. Total dry matter yields of tops and grain yields were highest at 200x 103 plants ha-1 (6214 and 3720 kg ha-1, respectively). The yield component most affected by population density was number of branches per plant, with values decreasing with increasing population density. The proportion of unfilled pods was highest at the highest population density. Total nitrogen (N) accumulation in the tops and in the grain was also at a maximum at 200x 103 plants ha-1. The rate of dry matter accumulation declined during pod filling at all population densities. N accumulation continued at high rates throughout the growing season except in the 400x 103 plants ha-1 population. There was a trend for residual dry matter and N in residues to increase with increasing population density. After grain and forage harvest of the first experiment, a crop of wheat (cv. Kite) was sown over the whole area to determine residual N available at anthesis and at maturity (experiment 2). The values of N accumulation in the wheat at maturity were 24 kg N ha-l for the maize treatment, 40-60 kg N ha-l for the soybean treatments and 69 kg N ha-1 for the fallow treatment. Grain yield and grain N followed the pattern of dry matter production and N accumulation at final harvest. The data suggest that soybean depletes soil N to a lesser extent than does maize. For the soybean treatments, there was a trend of increasing residual N at the 3 highest population densities (40-60 kg N ha-1). This was probably a result of an increase in N in leaf fall and in decaying tops and roots at the highest population density. The high value (57 kg N ha-l) at the lowest population density may be due to soybean plants at this density not using as much soil N as the other soybean treatments. No benefit in residual N was gained from planting soybeans at a density beyond the optimum for grain yield when residues were removed by forage harvesting.


1975 ◽  
Vol 23 (4) ◽  
pp. 523 ◽  
Author(s):  
LR Clark ◽  
MJ Dallwitz

In 1958-63 and 1964-71 the life systems of four kinds of test-forming psyllid that coexist on Eucalyptus blakelyi were investigated intensively in a comparative study of insect abundance. This paper deals mainly with C. albitextura, which was kept under observation from 1950 to 1974. (The others were two species of Glycaspis, Spondyliaspis sp, and Creiis costatus.) The results indicate that the differences in maximal abundance reached by the four kinds of psyllid are mainly the outcome of differences in their ability tg utilize the leaves of the host plant as a source of food, C. albitextura being much more effective than the other species. For the latter, it appears that the principal environmental determinant of abundance was the number of feeding places where nymphs could survive long enough to complete development. That number varied according to foliage and weather. C. albitextura also differed from the other species by having its population densities held for long periods far below the levels at which the food supply would be limiting, by restrictions imposed upon reproduction by adverse weather and foliage conditions (the latter being due partly to poor synchronization between the emergence of adults in spring and the occurrence of foliage attractive for oviposition), and by high mortalities due to natural enemies. The life system of C. albitextura lacks an element that can stabilize abundance at low population densities, but adverse environmental influences usually limit the rate of increase greatly when abundance is low. The magnitude of the average rate of increase to high levels of population density, and the length of time for which high average densities are maintained, depend upon the frequency with which favourable conditions of weather, foliage and predation combine to promote both survival and reproduction.


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