Field Gene Banks, Botanic Gardens, In Vitro, DNA and Pollen Conservation

2000 ◽  
pp. 92-107 ◽  
Author(s):  
J. G. Hawkes ◽  
N. Maxted ◽  
B. V. Ford-Lloyd
Keyword(s):  
Botanic Gardens ◽  
Gene Banks

In vitro methods of germ-plasm conservation

Genome ◽  
1989 ◽  
Vol 31 (2) ◽  
pp. 813-817 ◽  
Author(s):  
W. M. Roca ◽  
R. Chavez ◽  
M. L. Martin ◽  
D. I. Arias ◽  
G. Mafla ◽  
...  
Keyword(s):  
Germ Plasm ◽  
Plant Genetic Resources ◽  
Gene Bank ◽  
In Vitro Conservation ◽  
Isozyme Electrophoresis ◽  
In Vitro Methods ◽  
Gene Banks ◽  
Active Gene ◽  
Valuable Adjunct

For many crops with preferential vegetative propagation, or which are sterile, or have seed unresponsive to standard seed storage techniques, in vitro methods can provide a valuable adjunct to other germ plasm conservation strategies. Two types of in vitro gene banks are proposed: (i) an in vitro active gene bank where cultures are maintained under slow growth; of the few of these that exist, the cassava (Manihot) in vitro active gene bank of the Centro Internacional de Agricultura Tropical (CIAT) consists of over 4000 clones; (ii) an in vitro base gene bank, where cultures are cryopreserved; at present, none of this type exist. In vitro conservation offers a means of maintaining valuable gene combinations in a small space, protected against pest and disease attack, soil problems, and climatic changes, and with high multiplication potential. The main limitations are inability to regenerate plants of many important crops and the risk of genetic instability of cultures. A joint project of the International Board for Plant Genetic Resources and CIAT is underway to develop an in vitro based set of procedures for handling germ plasm, using cassava as a model, with culture maintenance, stability monitoring, and management data bases being considered. Results of recent work on in vitro conservation and related activities, i.e., germ-plasm collection, exchange, and characterization, will be presented and discussed, with special reference to Manihot.Key words: in vitro gene banks, cryopreservation, isozyme electrophoresis, genotype stability, Manihot esculenta Crantz.

scholarly journals Germplasm Conservation: Instrumental in Agricultural Biodiversity-A Review

2021 ◽  
Author(s):  
Veerala Priyanka ◽  
Rahul Kumar ◽  
Inderpreet Dhaliwal ◽  
Prashant Kaushik
Keyword(s):  
Agricultural Production ◽  
Slow Growth ◽  
Germplasm Conservation ◽  
Botanic Gardens ◽  
Genetic Composition ◽  
Plant Resources ◽  
Germplasm Exchange ◽  
Protection Strategies ◽  
Potential Use

Germplasm is a valuable natural resource in plant diversity that is crucial for its potential use. It provides knowledge about a species genetic composition. Germplasm protection strategies are not just planting hope threatened with extinction, they preserve medicinal and other essential plants on which survival rests. The successful use of genetic plant resources necessitates diligent collection, storage, analysis, documentation, and germplasm exchange. Slow growth cultures, cryopreservation, pollen and DNA banks, botanic gardens, genetic reserves and farmer’s fields are few conservation techniques. However, usage of an in vitro procedure with any chance of genetic instability leads to the destruction of the entire substance. Improved understanding of basic regeneration biology would, in turn, undoubtedly increase the capacity to regenerate plants from in vitro harvested explants, thus expanding selection possibilities. Germplasm conservation seeks to conserve endangered and vulnerable plant species worldwide for future proliferation and development; it is also the bedrock of agricultural production.

scholarly journals Guest Essay Global hosts and global pathogens: a perspective

2020 ◽  
pp. 5-17
Author(s):  
Janis Antonovics ◽  
Katherine Hayden
Keyword(s):  
Life Form ◽  
Microbial Interactions ◽  
Disease Spread ◽  
Rational Approach ◽  
Botanic Gardens ◽  
Natural Systems ◽  
Inspection And Quarantine ◽  
Plant Life Form ◽  
Population Numbers

Plant species are assailed by a remarkable diversity of pathogens, and these and other pests pose a serious direct risk to collections in botanic gardens as well as a potential source of pathogen escape. The high diversity of species in gardens combined with low population numbers minimises the likelihood of disease spread of specialist pathogens, but importation of novel pathogens is a constant concern. In parallel with natural systems, there is little data on pathogen loads in botanic gardens, on what accession policies minimise these and if such loads are likely to differ by country of origin or plant life form. Nevertheless, commonsense measures such as prohibiting the importation of plants in soil, shifting to seed and in vitro propagation, and inspection and quarantine on receiving and transferring plants should be implemented.This edition of Sibbaldia explores a variety of directions for improving our ability to develop strategies for dealing not just with pathogen threats, but with a more rational approach to pests and to microbial interactions that are a natural part of a plant’s heritage.

Micropropagation of Three Endemic Begonias Using Various Hormones Concentration and Culture Media Application

2021 ◽  
Vol 6 (2) ◽  
pp. 284-294
Author(s):  
Lily Ismaini ◽  
Intani Quarta Lailaty ◽  
Muhammad Efendi
Keyword(s):  
Analysis Of Variance ◽  
In Vitro Propagation ◽  
Growth Response ◽  
Culture Media ◽  
Ornamental Plant ◽  
Botanic Gardens ◽  
Growth Responses ◽  
Significance Level ◽  
Shoot Number

Three species of Begonias endemic to Java and Sumatra, namely Begonia leuserensis, Begonia atricha and Begonia scottii, were conserved in Cibodas Botanic Gardens as sources of germplasm for ornamental plant and/or medicines. However, the information on efficient hormones concentration and their culture media application through an in vitro propagation effort is still limited. Therefore, this study aimed to explain the growth response of three species of Begonias using various hormones concentrations and culture media through in vitro propagation. The culture media using Murashige & Skoog (MS) media that combinedwith 6-Benzyladenine (BA) dan Thidiazuron (TDZ) hormones in different concentrations i.e. 0.5 mg/L, 1 mg/L, 2 mg/L, and 3 mg/L. Observation parameter included shoot number, plantlets height, and leaves number. The data were analyzed using analysis of variance (ANOVA) with the F test at a 5% significance level. The results showed that three species of Begonias were observed to have different growth responses in the combination of MS+BA and MS+TDZ media. The combination of MS+TDZ media produces more shoots number, while the combination of MS+BA media influenced higher in leaves number. A concentration of 0.5 mg/L of hormone showed a good regeneration, therefore were recommended for in vitro propagation of Begonia species.

Ultrastructural Investigations of the Contractile Filaments of Amoebae

1974 ◽  
Vol 32 ◽  
pp. 188-189
Author(s):  
P.L. Moore
Keyword(s):  
Cytoplasmic Streaming ◽  
Three Dimensional ◽  
Freeze Fracture ◽  
Amoeboid Movement ◽  
Different Types ◽  
Chemical Conditions ◽  
Complete Interpretation

Previous freeze fracture results on the intact giant, amoeba Chaos carolinensis indicated the presence of a fibrillar arrangement of filaments within the cytoplasm. A complete interpretation of the three dimensional ultrastructure of these structures, and their possible role in amoeboid movement was not possible, since comparable results could not be obtained with conventional fixation of intact amoebae. Progress in interpreting the freeze fracture images of amoebae required a more thorough understanding of the different types of filaments present in amoebae, and of the ways in which they could be organized while remaining functional.The recent development of a calcium sensitive, demembranated, amoeboid model of Chaos carolinensis has made it possible to achieve a better understanding of such functional arrangements of amoeboid filaments. In these models the motility of demembranated cytoplasm can be controlled in vitro, and the chemical conditions necessary for contractility, and cytoplasmic streaming can be investigated. It is clear from these studies that “fibrils” exist in amoeboid models, and that they are capable of contracting along their length under conditions similar to those which cause contraction in vertebrate muscles.

In Vitro Induction of Crystals of MT Protein by Vinblastine-Colcemid in Mouse Spermatids

1974 ◽  
Vol 32 ◽  
pp. 132-133
Author(s):  
John J. Wolosewick ◽  
John H. D. Bryan
Keyword(s):  
Endoplasmic Reticulum ◽  
Smooth Endoplasmic Reticulum ◽  
Nuclear Ring ◽  
Rough Er ◽  
Distal Direction ◽  
In Vitro Induction

Early in spermiogenesis the manchette is rapidly assembled in a distal direction from the nuclear-ring-densities. The association of vesicles of smooth endoplasmic reticulum (SER) and the manchette microtubules (MTS) has been reported. In the mouse, osmophilic densities at the distal ends of the manchette are the organizing centers (MTOCS), and are associated with the SER. Rapid MT assembly and the lack of rough ER suggests that there is an existing pool of MT protein. Colcemid potentiates the reaction of vinblastine with tubulin and was used in this investigation to detect this protein.

Induction and Differentiation of Dental Epithelium in Vivo and in Vitro

1982 ◽  
Vol 40 ◽  
pp. 142-145
Author(s):  
E. J. Kollar
Keyword(s):  
Connective Tissue ◽  
Oral Mucosa ◽  
Basal Lamina ◽  
Functional Derivatives ◽  
Specific Source ◽  
Dental Epithelium ◽  
Connective Tissue Stroma

The differentiation and maintenance of many specialized epithelial structures are dependent on the underlying connective tissue stroma and on an intact basal lamina. These requirements are especially stringent in the development and maintenance of the skin and oral mucosa. The keratinization patterns of thin or thick cornified layers as well as the appearance of specialized functional derivatives such as hair and teeth can be correlated with the specific source of stroma which supports these differentiated expressions.

Immunoenzymatic demonstration of the simultaneous presence of transferrin, hemopexin and albumin in a same hepatocyte and their ultrastructural localization

1978 ◽  
Vol 36 (2) ◽  
pp. 88-89
Author(s):  
M. Kraemer ◽  
J. Foucrier ◽  
J. Vassy ◽  
M.T. Chalumeau
Keyword(s):  
Plasma Proteins ◽  
Rat Hepatocytes ◽  
Ultrastructural Localization ◽  
Carrier Proteins ◽  
Normal Cells ◽  
Adult Rat ◽  
Adult Rat Hepatocytes ◽  
Monospecific Antisera ◽  
Different Levels

Some authors using immunofluorescent techniques had already suggested that some hepatocytes are able to synthetize several plasma proteins. In vitro studies on normal cells or on cells issued of murine hepatomas raise the same conclusion. These works could be indications of an hepatocyte functionnal non-specialization, meanwhile the authors never give direct topographic proofs suitable with this hypothesis.The use of immunoenzymatic techniques after obtention of monospecific antisera had seemed to us useful to bring forward a better knowledge of this problem. We have studied three carrier proteins (transferrin = Tf, hemopexin = Hx, albumin = Alb) operating at different levels in iron metabolism by demonstrating and localizing the adult rat hepatocytes involved in their synthesis.Immunological, histological and ultrastructural methods have been described in a previous work.

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