scholarly journals Do workers share in firm success? Pass-through estimates for New Zealand

2021 ◽  
Author(s):  
Corey Allan ◽  
David C. Maré
2021 ◽  
Author(s):  
◽  
Elle Fairgray

<p>Water is a fundamental component of New Zealand’s landscape, culture, history and identity. It is moving, changing form, accumulating and dispersing, it is ever changing never in the same context twice. Rivers are a single representation of this process in which we experience water in the landscape.  New Zealand has beautiful and intense water ways that pass through urban environments, yet due to the flood protection measures in place, they are disconnected from the urban environment. They are difficult to access and do not hold a presence in our growing urban environment which they once had significance in.  Stopbanks are the most common form of river flood protection infrastructure in New Zealand. They treat the river as a static element without giving them the space to move, flood and meander. They create a physical barrier between the urban environment and river space and do not respond to the differences of rivers and urban environments.  Growing urbanisation is increasing the pressure on stormwater infrastructure and growing the risk and effects of flooding. Increasing magnitude and frequency of rainfall events is only putting more pressure on flood protection infrastructure and stopbank infrastructure is crumbling under the pressure. Urban environments are requiring a larger level of flood protection that the traditional stopbank can provide.  This thesis is an investigation into the role of stopbanks for flood protection in urban river spaces and their effect of the experiential and ecological experience of the river. This investigation, developed through an analysis of the Waiwhakaiho River in New Plymouth, the Waikanae River in Kapiti and the Waipoua River in the Waiarapa informs a redesign of flood protection measures in New Zealand medium sized towns to repair the disconnection of the urban environment to the river.</p>


2021 ◽  
Author(s):  
◽  
Peter Robin Todd

<p>Macroscopic and histological observations of the gonads from 1,739 non-migrant freshwater eels, the shortfin Anguilla australis schmidtii Phillipps and the longfin A. dieffenbachii Gray, showed that they pass through seven stages of development. Shortfins become sexually differentiated at body lengths of 35.0cm to 56.9cm and longfins at lengths of 50.0cm to 67.0cm. No intersexual stage was present, as in A. anguilla L., and although 1% of 350 migrating longfin males examined contained ribbon-like testes, the typical lobed organ of Syrski (testis) can be used as diagnostic of maleness. Histologically, the maximum stage of development attained in the non-migrant, immature stage, was spermatogonia in the males and vacuolated oocytes in females. At the time of seaward migration, based on gonad histology, gonadosomatic indices and ova diameters, migrating longfins were more sexually developed than shortfins. These differences may relate to the location of different oceanic spawning areas: that for the longfin possibly being closer to New Zealand. The autumnal migratory runs, from March to May, of the sexually maturing adults in the Makara stream showed no particular species or sex sequence. The movement of eels was coincident with a rise in stream level and the second half of the lunar cycle. Other relevant environmental factors are discussed. In Lake 0noke peak catches of seaward migrating shortfins were made before the longfins and movements of eels occurred throughout the lunar cycle. Once at sea, the eels apparently disappear. A published note is included on the first eel of the New Zealand species, a longfin female, to be caught at sea. Age determinations from 995 eels were made by otoliths, which were burnt lightly to intensify the growth zones for reading purposes. Shortfin males are younger than females at migration. Longfins are older than shortfins at migration but the males are younger than the females. In the non-migrant stage, sexually undifferentiated shortfins grow more slowly relative to the males, and males relatively more slowly than the females. Similar but less significant differences in growth occur in longfins. Migrant males held in seawater were induced to mature and spawn with injections of mammalian hormones or carp pituitaries, over temperatures of 11.8 degrees C to 28 degrees C. The maturation period was dependent on temperature. Testes of experimental eels that survived maturation regressed to the pre-migrant or migrant stage. Two eels that had regressed were induced to mature a second time. Females held at 20 degrees C and injected with mammalian hormones showed significant increases in sexual development but died before maturity. Females injected with carp pituitaries matured and spawned. Mature longfin eggs, 0.9mm to 1.2mm in diametar, and mature shortfin eggs, 0.9mm to 1.2mm in diameter, are translucent and contain one to many oil globules. A blastodisc formed in water hardened eggs but attempts at fertilization were unsuccessful. Gametogenesis, observed from non-migrant, migrant and hormone injected eels is similar to that described for other teleosts. Electron microscope observations showed parallel features of spermiogenesis in both species. Mature spermatozoa have crescent shaped heads with an anteriorly placed mitochondrion. A flagellum of the unusual 9 + 0 pattern arises from the posterior region of the head, and a short, striated rod-like structure is positioned adjacent to the main flagellum. A complex of subfibrils which extend along either side of the head to the mitochondrion arise from the proximal centriole.</p>


2021 ◽  
Author(s):  
◽  
Peter Robin Todd

<p>Macroscopic and histological observations of the gonads from 1,739 non-migrant freshwater eels, the shortfin Anguilla australis schmidtii Phillipps and the longfin A. dieffenbachii Gray, showed that they pass through seven stages of development. Shortfins become sexually differentiated at body lengths of 35.0cm to 56.9cm and longfins at lengths of 50.0cm to 67.0cm. No intersexual stage was present, as in A. anguilla L., and although 1% of 350 migrating longfin males examined contained ribbon-like testes, the typical lobed organ of Syrski (testis) can be used as diagnostic of maleness. Histologically, the maximum stage of development attained in the non-migrant, immature stage, was spermatogonia in the males and vacuolated oocytes in females. At the time of seaward migration, based on gonad histology, gonadosomatic indices and ova diameters, migrating longfins were more sexually developed than shortfins. These differences may relate to the location of different oceanic spawning areas: that for the longfin possibly being closer to New Zealand. The autumnal migratory runs, from March to May, of the sexually maturing adults in the Makara stream showed no particular species or sex sequence. The movement of eels was coincident with a rise in stream level and the second half of the lunar cycle. Other relevant environmental factors are discussed. In Lake 0noke peak catches of seaward migrating shortfins were made before the longfins and movements of eels occurred throughout the lunar cycle. Once at sea, the eels apparently disappear. A published note is included on the first eel of the New Zealand species, a longfin female, to be caught at sea. Age determinations from 995 eels were made by otoliths, which were burnt lightly to intensify the growth zones for reading purposes. Shortfin males are younger than females at migration. Longfins are older than shortfins at migration but the males are younger than the females. In the non-migrant stage, sexually undifferentiated shortfins grow more slowly relative to the males, and males relatively more slowly than the females. Similar but less significant differences in growth occur in longfins. Migrant males held in seawater were induced to mature and spawn with injections of mammalian hormones or carp pituitaries, over temperatures of 11.8 degrees C to 28 degrees C. The maturation period was dependent on temperature. Testes of experimental eels that survived maturation regressed to the pre-migrant or migrant stage. Two eels that had regressed were induced to mature a second time. Females held at 20 degrees C and injected with mammalian hormones showed significant increases in sexual development but died before maturity. Females injected with carp pituitaries matured and spawned. Mature longfin eggs, 0.9mm to 1.2mm in diametar, and mature shortfin eggs, 0.9mm to 1.2mm in diameter, are translucent and contain one to many oil globules. A blastodisc formed in water hardened eggs but attempts at fertilization were unsuccessful. Gametogenesis, observed from non-migrant, migrant and hormone injected eels is similar to that described for other teleosts. Electron microscope observations showed parallel features of spermiogenesis in both species. Mature spermatozoa have crescent shaped heads with an anteriorly placed mitochondrion. A flagellum of the unusual 9 + 0 pattern arises from the posterior region of the head, and a short, striated rod-like structure is positioned adjacent to the main flagellum. A complex of subfibrils which extend along either side of the head to the mitochondrion arise from the proximal centriole.</p>


2021 ◽  
Author(s):  
◽  
Elle Fairgray

<p>Water is a fundamental component of New Zealand’s landscape, culture, history and identity. It is moving, changing form, accumulating and dispersing, it is ever changing never in the same context twice. Rivers are a single representation of this process in which we experience water in the landscape.  New Zealand has beautiful and intense water ways that pass through urban environments, yet due to the flood protection measures in place, they are disconnected from the urban environment. They are difficult to access and do not hold a presence in our growing urban environment which they once had significance in.  Stopbanks are the most common form of river flood protection infrastructure in New Zealand. They treat the river as a static element without giving them the space to move, flood and meander. They create a physical barrier between the urban environment and river space and do not respond to the differences of rivers and urban environments.  Growing urbanisation is increasing the pressure on stormwater infrastructure and growing the risk and effects of flooding. Increasing magnitude and frequency of rainfall events is only putting more pressure on flood protection infrastructure and stopbank infrastructure is crumbling under the pressure. Urban environments are requiring a larger level of flood protection that the traditional stopbank can provide.  This thesis is an investigation into the role of stopbanks for flood protection in urban river spaces and their effect of the experiential and ecological experience of the river. This investigation, developed through an analysis of the Waiwhakaiho River in New Plymouth, the Waikanae River in Kapiti and the Waipoua River in the Waiarapa informs a redesign of flood protection measures in New Zealand medium sized towns to repair the disconnection of the urban environment to the river.</p>


1999 ◽  
Vol 190 ◽  
pp. 563-566
Author(s):  
J. D. Pritchard ◽  
W. Tobin ◽  
J. V. Clausen ◽  
E. F. Guinan ◽  
E. L. Fitzpatrick ◽  
...  

Our collaboration involves groups in Denmark, the U.S.A. Spain and of course New Zealand. Combining ground-based and satellite (IUEandHST) observations we aim to determine accurate and precise stellar fundamental parameters for the components of Magellanic Cloud Eclipsing Binaries as well as the distances to these systems and hence the parent galaxies themselves. This poster presents our latest progress.


Author(s):  
J. H. Butler ◽  
C. J. Humphreys

Electromagnetic radiation is emitted when fast (relativistic) electrons pass through crystal targets which are oriented in a preferential (channelling) direction with respect to the incident beam. In the classical sense, the electrons perform sinusoidal oscillations as they propagate through the crystal (as illustrated in Fig. 1 for the case of planar channelling). When viewed in the electron rest frame, this motion, a result of successive Bragg reflections, gives rise to familiar dipole emission. In the laboratory frame, the radiation is seen to be of a higher energy (because of the Doppler shift) and is also compressed into a narrower cone of emission (due to the relativistic “searchlight” effect). The energy and yield of this monochromatic light is a continuously increasing function of the incident beam energy and, for beam energies of 1 MeV and higher, it occurs in the x-ray and γ-ray regions of the spectrum. Consequently, much interest has been expressed in regard to the use of this phenomenon as the basis for fabricating a coherent, tunable radiation source.


Author(s):  
Robert M. Glaeser

It is well known that a large flux of electrons must pass through a specimen in order to obtain a high resolution image while a smaller particle flux is satisfactory for a low resolution image. The minimum particle flux that is required depends upon the contrast in the image and the signal-to-noise (S/N) ratio at which the data are considered acceptable. For a given S/N associated with statistical fluxtuations, the relationship between contrast and “counting statistics” is s131_eqn1, where C = contrast; r2 is the area of a picture element corresponding to the resolution, r; N is the number of electrons incident per unit area of the specimen; f is the fraction of electrons that contribute to formation of the image, relative to the total number of electrons incident upon the object.


Author(s):  
Ronald S. Weinstein ◽  
N. Scott McNutt

The Type I simple cold block device was described by Bullivant and Ames in 1966 and represented the product of the first successful effort to simplify the equipment required to do sophisticated freeze-cleave techniques. Bullivant, Weinstein and Someda described the Type II device which is a modification of the Type I device and was developed as a collaborative effort at the Massachusetts General Hospital and the University of Auckland, New Zealand. The modifications reduced specimen contamination and provided controlled specimen warming for heat-etching of fracture faces. We have now tested the Mass. General Hospital version of the Type II device (called the “Type II-MGH device”) on a wide variety of biological specimens and have established temperature and pressure curves for routine heat-etching with the device.


Author(s):  
George Christov ◽  
Bolivar J. Lloyd

A new high intensity grid cap has been designed for the RCA-EMU-3 electron microscope. Various parameters of the new grid cap were investigated to determine its characteristics. The increase in illumination produced provides ease of focusing on the fluorescent screen at magnifications from 1500 to 50,000 times using an accelerating voltage of 50 KV.The EMU-3 type electron gun assembly consists of a V-shaped tungsten filament for a cathode with a thin metal threaded cathode shield and an anode with a central aperture to permit the beam to course the length of the column. The cathode shield is negatively biased at a potential of several hundred volts with respect to the filament. The electron beam is formed by electrons emitted from the tip of the filament which pass through an aperture of 0.1 inch diameter in the cap and then it is accelerated by the negative high voltage through a 0.625 inch diameter aperture in the anode which is at ground potential.


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