Is the subspecies classification of the freshwater eels Anguilla australis australis Richardson and A. a. schmidtii Phillipps still valid?

1999 ◽  
Vol 50 (3) ◽  
pp. 261 ◽  
Author(s):  
L. H. Dijkstra ◽  
D. J. Jellyman

The validity of the subspecies classification of Anguilla australis was reviewed by sequencing the control region of mitochondrial DNA. Samples of A. a. australis (Australia) and A. a. schmidtii (New Zealand), collected from two sites within each country were compared by analysis of molecular variance (AMOVA) and neighbour joining. There was no molecular evidence to support the present subspecies designation and they would be more appropriately merged into the single classification of A. australis, the Australasian shortfinned eel. As Australian and New Zealand populations of this species share a common gene pool, fisheries management needs to be carried out cooperatively between the two countries.

2021 ◽  
Author(s):  
◽  
Donald John Jellyman

<p>The early freshwater life of the two species of New Zealand freshwater eels, Anguilla australis schmidtii Phillipps and A. dieffenbachii Gray was studied involving an examination of 8131 glass-eels, 5275 migratory elvers, and 4291 resident eels of less than 26 cm. Most eels were collected from the Makara Stream, Wellington by set-net, hand-net and electric fishing. These extensive samples together with subsidiary collections from elsewhere in New Zealand show that glass-eels of both species arrive in fresh-water from July to December. Their otoliths indicate a marine larval life of about 18 months but it is not possible as yet to locate the precise oceanic spawning areas. Migratory movements of glass-eels are in two phases: an invasion of fresh-water from the sea and an upstream migration. The former occurs only at night with a periodicity corresponding to the daily ebb-flood tidal rhythms. There is a seasonal reversal in this response which is attributable to the onset of the behavioural transition taking place prior to the second migratory phase. Increased pigmentation and changes in response to light, flowing fresh-water and schooling tendencies characterise this latter migration which occurs primarily at spring tide periods. Such juvenile eels show specific habitat preferences and a high degree of olfactory differentiation of water types. This behaviour, together with pigment development and physical tolerances, was studied in the laboratory. Measurements of invading glass-eels show that mean length, weight and condition all decline throughout the season of arrival but mean vertebral numbers remain constant. An upstream migration of small eels (elvers) occurs each summer and is readily observed at many hydro-electric stations. These migrations, comprising eels of mixed sizes and age groups, penetrate progressively further upstream each year. In both species, scales begin formation at body lengths of 16.5-20 cm. All features of scale formation, including the number of scale rings, are related to length with relative differences in rate of development occurring between the species. In contrast to scale rings, otolith rings are annual in formation and become visible after grinding or burning the otolith. Growth rates established for 273 eels to 29 cm in length from the Makara Stream, Wellington, are slow, with mean annual increments of 2.2 and 2.1 cm respectively for shortfins and longfins. In contrast, shortfins from a coastal lake near Wellington reach 26 cm in their third year of freshwater life. Length-weight relationships for small eels are given together with mean monthly condition factors. Growth studies on elvers held in a multiple tank unit in which temperature, density, and amount and frequency of feeding could be controlled, show that young eels grow more slowly than normal under such conditions. However, growth appears optimum at 20 degrees C with a feeding rate of 5-7% body weight per day. Feeding efficiency decreases with higher temperatures. At both glass-eel and elver stages, shortfins adapt and survive better under artificial conditions.</p>


Genetics ◽  
1992 ◽  
Vol 131 (2) ◽  
pp. 479-491 ◽  
Author(s):  
L Excoffier ◽  
P E Smouse ◽  
J M Quattro

Abstract We present here a framework for the study of molecular variation within a single species. Information on DNA haplotype divergence is incorporated into an analysis of variance format, derived from a matrix of squared-distances among all pairs of haplotypes. This analysis of molecular variance (AMOVA) produces estimates of variance components and F-statistic analogs, designated here as phi-statistics, reflecting the correlation of haplotypic diversity at different levels of hierarchical subdivision. The method is flexible enough to accommodate several alternative input matrices, corresponding to different types of molecular data, as well as different types of evolutionary assumptions, without modifying the basic structure of the analysis. The significance of the variance components and phi-statistics is tested using a permutational approach, eliminating the normality assumption that is conventional for analysis of variance but inappropriate for molecular data. Application of AMOVA to human mitochondrial DNA haplotype data shows that population subdivisions are better resolved when some measure of molecular differences among haplotypes is introduced into the analysis. At the intraspecific level, however, the additional information provided by knowing the exact phylogenetic relations among haplotypes or by a nonlinear translation of restriction-site change into nucleotide diversity does not significantly modify the inferred population genetic structure. Monte Carlo studies show that site sampling does not fundamentally affect the significance of the molecular variance components. The AMOVA treatment is easily extended in several different directions and it constitutes a coherent and flexible framework for the statistical analysis of molecular data.


2021 ◽  
Author(s):  
◽  
Donald John Jellyman

<p>The early freshwater life of the two species of New Zealand freshwater eels, Anguilla australis schmidtii Phillipps and A. dieffenbachii Gray was studied involving an examination of 8131 glass-eels, 5275 migratory elvers, and 4291 resident eels of less than 26 cm. Most eels were collected from the Makara Stream, Wellington by set-net, hand-net and electric fishing. These extensive samples together with subsidiary collections from elsewhere in New Zealand show that glass-eels of both species arrive in fresh-water from July to December. Their otoliths indicate a marine larval life of about 18 months but it is not possible as yet to locate the precise oceanic spawning areas. Migratory movements of glass-eels are in two phases: an invasion of fresh-water from the sea and an upstream migration. The former occurs only at night with a periodicity corresponding to the daily ebb-flood tidal rhythms. There is a seasonal reversal in this response which is attributable to the onset of the behavioural transition taking place prior to the second migratory phase. Increased pigmentation and changes in response to light, flowing fresh-water and schooling tendencies characterise this latter migration which occurs primarily at spring tide periods. Such juvenile eels show specific habitat preferences and a high degree of olfactory differentiation of water types. This behaviour, together with pigment development and physical tolerances, was studied in the laboratory. Measurements of invading glass-eels show that mean length, weight and condition all decline throughout the season of arrival but mean vertebral numbers remain constant. An upstream migration of small eels (elvers) occurs each summer and is readily observed at many hydro-electric stations. These migrations, comprising eels of mixed sizes and age groups, penetrate progressively further upstream each year. In both species, scales begin formation at body lengths of 16.5-20 cm. All features of scale formation, including the number of scale rings, are related to length with relative differences in rate of development occurring between the species. In contrast to scale rings, otolith rings are annual in formation and become visible after grinding or burning the otolith. Growth rates established for 273 eels to 29 cm in length from the Makara Stream, Wellington, are slow, with mean annual increments of 2.2 and 2.1 cm respectively for shortfins and longfins. In contrast, shortfins from a coastal lake near Wellington reach 26 cm in their third year of freshwater life. Length-weight relationships for small eels are given together with mean monthly condition factors. Growth studies on elvers held in a multiple tank unit in which temperature, density, and amount and frequency of feeding could be controlled, show that young eels grow more slowly than normal under such conditions. However, growth appears optimum at 20 degrees C with a feeding rate of 5-7% body weight per day. Feeding efficiency decreases with higher temperatures. At both glass-eel and elver stages, shortfins adapt and survive better under artificial conditions.</p>


Plant Disease ◽  
2003 ◽  
Vol 87 (11) ◽  
pp. 1376-1383 ◽  
Author(s):  
J. X. Zhang ◽  
W. G. D. Fernando ◽  
A. G. Xue

Fifty-eight isolates of Mycosphaerella pinodes, collected from western Canada, New Zealand, France, Australia, the United Kingdom, and Ireland, were analyzed for pathogenic and genetic variation according to their virulence on six differential cultivars of field pea (AC Tamor, Bohatyre, Danto, Majoret, Miko, and Radley) and amplified fragment length polymorphism markers. The 56 isolates were classified into 15 pathotypes. Pathotype 1 consisted of 31 isolates that were virulent on all six pea differential cultivars. Pathotypes 14 and 15 consisted of eight isolates that were avirulent on all six differential cultivars or virulent on one of six differential cultivars. The analysis of molecular variance showed that 57.2% of the total variation was caused by differences among populations, and 42.8% was due to molecular diversity within populations. Phylogenetic analysis of molecular variation of isolates showed that most of the Canadian isolates and four Australian isolates formed two clustered groups, respectively, regardless of virulence on the six differential cultivars. Isolates from New Zealand were geographically clustered into two groups. However, the isolates from France, Ireland, and the United Kingdom were clustered with the Canadian isolates.


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>


2010 ◽  
Vol 32 (1) ◽  
pp. 25-32 ◽  
Author(s):  
Anita Kloss-Brandstätter ◽  
Dominic Pacher ◽  
Sebastian Schönherr ◽  
Hansi Weissensteiner ◽  
Robert Binna ◽  
...  

1964 ◽  
Vol 16 (2) ◽  
pp. 6-10
Author(s):  
R. P. Hargreaves ◽  
W. J. Maunder

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