Age Structure and Growth in the Zamda Toad, Bufotes zamdaensis (Anura, Bufonidae)

2021 ◽  
Vol 28 (3) ◽  
pp. 138-144
Author(s):  
Sergey M. Lyapkov ◽  
Artem A. Kidov ◽  
Irina V. Stepankova ◽  
Kirill A. Afrin ◽  
Spartak N. Litvinchuk
Keyword(s):  
Growth Rate ◽  
Age Structure ◽  
Related Species ◽  
Mean Value ◽  
Himachal Pradesh ◽  
Closely Related Species

The paper provides the first data about age structure and growth of the Zamda toad, Bufotes zamdaensis (Boulenger, 1882), from the Himachal Pradesh State (India). The study of age structure of toads was carried out using skeletochronology. The minimal and maximal ages in males of B. zamdaensis were 4 and 7 years, respectively, with mean age of 5.4 years. The majority of males (60%) were 5 years old. The age in females ranged from 5 to 9 years with mean value of 6.1 years. The majority of females (71%) were 5 – 6 years old. Males of B. zamdaensis can reach maturation after four winterings and females after five winterings. Unlike closely related species B. latastii, the growth rate in both sexes does not decrease significantly after the 1st and 2nd wintering and remains high after the 3rd and 4th wintering.

Ecological Traits of the Eucalyptus L'hérit Subgenera Monocalyptus and Symphyomyrtus

1989 ◽  
Vol 37 (3) ◽  
pp. 207 ◽  
Author(s):  
IR Noble
Keyword(s):  
Growth Rate ◽  
Growth Rates ◽  
Root Morphology ◽  
Related Species ◽  
Early Growth ◽  
Growth Patterns ◽  
Leaf Chemistry ◽  
Ecological Traits ◽  
Closely Related Species ◽  
Genus Eucalyptus

The genus Eucalyptus L'Hérit. dominates most of the forests and woodlands of Australia. Many stands consist of intimate mixtures of species from different subgenera. The ecological traits of the two largest subgenera, Symphyomyrtus and Monocalyptus, are reviewed. Consistent differences in herbivore and parasite damage to leaves; in water relations; in tolerance to waterlogging, flooding, salinity and frost; in nutrient usage; in response to Phytophthora cinnamorni; and in early growth patterns are described. These can be summarised as differences in leaf chemistry; in root morphology, chemistry and activity; and in early growth rates. It is suggested that the differences in the ecological traits, and especially in the early growth rate, may help explain the coexistence of closely related species of similar habits in eucalypt communities.

Age Structure and Growth in the Lataste’s Toad, Bufotes latastii (Anura: Bufonidae)

2020 ◽  
Vol 27 (3) ◽  
pp. 165-171 ◽  
Author(s):  
Sergey Marlenovich Lyapkov ◽  
Artem Aleksandrovich Kidov ◽  
Irina Vladimirovna Stepankova ◽  
Kirill Aleksandrovich Afrin ◽  
Spartak Nikolaevich Litvinchuk
Keyword(s):  
Growth Rate ◽  
Body Length ◽  
Age Structure ◽  
Mean Value ◽  
The Body ◽  
Jammu And Kashmir ◽  
Different Ages ◽  
Length Increment

The paper provided the first data about age structure and growth of the Lataste’s toad, Bufotes latastii (Boulenger, 1882), from the Jammu and Kashmir State (India). The study of age structure of toads was carried out using skeletochronology. The minimal and maximal ages in males of B. latastii were 3 and 10 years, respectively, with mean age of 6.0 years. The majority of males (70%) were 5 or 6 years old. The age in females ranged from 4 to 10 years with mean value of 5.9 years. The majority of females (71%) were 4 – 6 years old. Males of B. latastii can reach maturation after three winterings and females after four winterings. The body length increment in males is 3.6 times, whereas in females is 3.7 – 4.0 times. After maturation, the growth rate is retarded and the individuals of different ages did not differ in its body length. In spite of maximal age of 10 years in both sexes, the largest male was 5 years old and the largest female was 4 years old.

Microsatellite Marker: Importance and Implications of Cross-genome Analysis for Finger Millet (Eleusine coracana (L.) Gaertn)

2020 ◽  
Vol 9 (3) ◽  
pp. 160-170
Author(s):  
Thumadath P.A. Krishna ◽  
Maharajan Theivanayagam ◽  
Gurusunathan V. Roch ◽  
Veeramuthu Duraipandiyan ◽  
Savarimuthu Ignacimuthu
Keyword(s):  
Molecular Marker ◽  
Microsatellite Markers ◽  
Ssr Markers ◽  
Genome Analysis ◽  
Related Species ◽  
Finger Millet ◽  
Crop Improvement ◽  
Human Beings ◽  
Closely Related Species ◽  
Genome Amplification

Finger millet is a superior staple food for human beings. Microsatellite or Simple Sequence Repeat (SSR) marker is a powerful tool for genetic mapping, diversity analysis and plant breeding. In finger millet, microsatellites show a higher level of polymorphism than other molecular marker systems. The identification and development of microsatellite markers are extremely expensive and time-consuming. Only less than 50% of SSR markers have been developed from microsatellite sequences for finger millet. Therefore, it is important to transfer SSR markers developed for related species/genus to finger millet. Cross-genome transferability is the easiest and cheapest method to develop SSR markers. Many comparative mapping studies using microsatellite markers clearly revealed the presence of synteny within the genomes of closely related species/ genus. Sufficient homology exists among several crop plant genomes in the sequences flanking the SSR loci. Thus, the SSR markers are beneficial to amplify the target regions in the finger millet genome. Many SSR markers were used for the analysis of cross-genome amplification in various plants such as Setaria italica, Pennisetum glaucum, Oryza sativa, Triticum aestivum, Zea mays and Hordeum vulgare. However, there is very little information available about cross-genome amplification of these markers in finger millet. The only limited report is available for the utilization of cross-genome amplified microsatellite markers in genetic analysis, gene mapping and other applications in finger millet. This review highlights the importance and implication of microsatellite markers such as genomic SSR (gSSR) and Expressed Sequence Tag (EST)-SSR in cross-genome analysis in finger millet. Nowadays, crop improvement has been one of the major priority areas of research in agriculture. The genome assisted breeding and genetic engineering plays a very crucial role in enhancing crop productivity. The rapid advance in molecular marker technology is helpful for crop improvement. Therefore, this review will be very helpful to the researchers for understanding the importance and implication of SSR markers in closely related species.

Genetic Complexity Underlying Hybrid Male Sterility in Drosophila

Genetics ◽  
2004 ◽  
Vol 166 (2) ◽  
pp. 789-796 ◽  
Author(s):  
Kyoichi Sawamura ◽  
John Roote ◽  
Chung-I Wu ◽  
Masa-Toshi Yamamoto
Keyword(s):  
Male Sterility ◽  
Related Species ◽  
Synergistic Effects ◽  
Female Sterility ◽  
Hybrid Male ◽  
Hybrid Female ◽  
Hybrid Male Sterility ◽  
Closely Related Species ◽  
Genetic Complexity ◽  
Recessive Genes

Abstract Recent genetic analyses of closely related species of Drosophila have indicated that hybrid male sterility is the consequence of highly complex synergistic effects among multiple genes, both conspecific and heterospecific. On the contrary, much evidence suggests the presence of major genes causing hybrid female sterility and inviability in the less-related species, D. melanogaster and D. simulans. Does this contrast reflect the genetic distance between species? Or, generally, is the genetic basis of hybrid male sterility more complex than that of hybrid female sterility and inviability? To clarify this point, the D. simulans introgression of the cytological region 34D-36A to the D. melanogaster genome, which causes recessive male sterility, was dissected by recombination, deficiency, and complementation mapping. The 450-kb region between two genes, Suppressor of Hairless and snail, exhibited a strong effect on the sterility. Males are (semi-)sterile if this region of the introgression is made homozygous or hemizygous. But no genes in the region singly cause the sterility; this region has at least two genes, which in combination result in male sterility. Further, the males are less fertile when heterozygous with a larger introgression, which suggests that dominant modifiers enhance the effects of recessive genes of male sterility. Such an epistatic view, even in the less-related species, suggests that the genetic complexity is special to hybrid male sterility.

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