INTRODUCTION. Internal Organization of the Plant Body. Summary of Types of Cells and Tissues. General References. DEVELOPMENT OF THE SEED PLANT. The Embryo. From embryo to the Adult Plant. Apical Meristems and Their Derivatives. Differentiation, Specialization, and Morphogenesis. References. THE CELL. Cytoplasm. Nucleus. Plastids. Mitochondria. Microbodies. Vacuoles. Paramural Bodies. Ribosomes. Dictyosomes. Endoplasmic Reticulum. Lipid Globules. Microtubules. Ergastic Substances. References. CELL WALL. Macromolecular Components and Their Organization in the Wall. Cell Wall Layers. Intercellular Spaces. Pits, Primary Pit--Fields, and Plasmodesmata. Origin of Cell Wall During Cell Division. Growth of Cell Wall. References. PARENCHYMA AND COLLENCHYMA. Parenchyma. Collenchyma. References. SCLERENCHYMA. Sclereids. Fibers. Development of Sclereids and Fibers. References. EPIDERMIS. Composition. Developmental Aspects. Cell Wall. Stomata. Trichomes. References. XYLEM: GENERAL STRUCTURE AND CELL TYPES. Gross Structure of Secondary Xylem. Cell Types in the Secondary Xylem. Primary Xylem. Differentiation of Tracheary Elements. References. XYLEM: VARIATION IN WOOD STRUCTURE. Conifer Wood. Dicotyledon Wood. Some Factors in Development of Secondary Xylem. Identification of Wood. References. VASCULAR CAMBIUM. Organization of Cambium. Developmental Changes in the Initial Layer. Patterns and Causal Relations in Cambial Activity. References. PHLOEM. Cell Types. Primary Phloem. Secondary Phloem. References. PERIDERM. Structure of Periderm and Related Tissues. Development of Periderm. Outer Aspect of Bark in Relation to Structure. Lenticels. References. SECRETORY STRUCTURES. External Secretory Structures. Internal Secretory Structures. References. THE ROOT: PRIMARY STATE OF GROWTH. Types of Roots. Primary Structure. Development. References. THE ROOT: SECONDARY STATE OF GROWTH AND ADVENTITIOUS ROOTS. Common Types of Secondary Growth. Variations in Secondary Growths. Physiologic Aspects of Secondary Growth in Roots. Adventitious Roots. References. THE STEM: PRIMARY STATE OF GROWTH. External Morphology. Primary Structure. Development. References. THE STEM: SECONDARY GROWTH AND STRUCTURAL TYPES. Secondary Growth. Types of Stems. References. THE LEAF: BASIC STRUCTURE AND DEVELOPMENT. Morphology. Histology of Angiosperm Leaf. Development. Abscission. References. THE LEAF: VARIATIONS IN STRUCTURE. Leaf Structure and Environment. Dicotyledon Leaves. Monocotyledon Leaves. Gymnosperm Leaves. References. THE FLOWER: STRUCTURE AND DEVELOPMENT. Concept. Structure. Development. References. THE FLOWER: REPRODUCTIVE CYCLE. Microsporogenesis. Pollen. Male Gametophyte. Megasporogenesis. Female Gametophyte. Fertilization. References. THE FRUIT. Concept and Classification. The Fruit Wall. Fruit Types. Fruit Growths. Fruit Abscission. References. THE SEED. Concept and Morphology. Seed Development. Seed Coat. Nutrient Storage Tissues. References. EMBRYO AND SEEDLING. Mature Embryo. Development of Embryo. Classification of Embryos. Seedling. References. Glossary. Index.

Anatomy of Seed Plants

Chitosan as a potential natural compound to control pre and postharvest diseases of horticultural commodities

Heterokaryon fonnation between different fungal individuals is an important component of many fungal life cycles and may serve as the first step in the parasexual cycle and the transmission of hypovirulent factors such as dsRNAs. Heterokaryosis also is a means by which nonnally haploid fungi may enjoy the benefits of functional diploidy, such as complementation or heterosis. In plant pathogenic fungi, the entity that emerges following heterokaryosis may differ from its constituents in aggressiveness or host range; some of these aspects have been reviewed in previous volumes in this series (9, 28, 45, 62, 72, 112, 114, 117, 143, 154, 158, 160). In most heterothallic fungi, the fonnation of a heterokaryon between two genetically different haploid strains is an essential part of the life cycle. Such heterokaryons may be quite stable and persist vegetatively for an indefinite period of time or may last only long enough for the component haploid nuclei to fuse and then immediately undergo meiosis. In many fungi, sexual and vegetative heterokaryons are quite distinct from one another. Strains capable of fonning a successful sexual heterokaryon may be unable to fonn a successful vegetative heterokaryon and vice versa. Strains that are capable of fonning these types of heterokaryons are referred to as "sexually" or "vegetatively" compatible, respectively. Strains that are vege­ tatively compatible with one another are frequently described as members of the same vegetative compatibility group, or VCG. Sexual compatibility is usually governed by one or more mating-type loci that may have two or more alleles (58, 62). Vegetative compatibility may be governed by the mating-type loci in some fungi, e.g. many basidiomycetes, but there also are examples in which a separate set of genes controls the fonnation and stability of these vegetative heterokaryons.

Fungal vegetative compatibility

Burgeoning consumer interest in organically produced foods has made organic farming one of the fastest growing segments of agriculture. This growth has not been supported adequately by rigorous research to address challenges such as arthropod pest management. The research that has been conducted, however, is complemented by research in aspects of conventional agriculture that may have applicability in organic systems, as well as by research in underpinning fields such as applied ecology. This article synthesizes the available literature in relation to a conceptual model of arthropod pest management strategies suitable for organic systems. The present work uses the four phases of the model to review the strategies in an agroecological context and provides a synthesis of the factors that influence the success of each phase. Rather than constituting a fringe science, pest management research for organic systems draws on cutting edge science in fields such as landscape and chemical ecology and has a bright future.

/pdf/arthropod-pest-management-in-organic-crops-1rmgtgljyj.pdf

Arthropod pest management in organic crops

Farmers are facing serious plant protection issues and phytosanitary risks, in particular in the tropics. Such issues are food insecurity, lower income in traditional low- input agroecosystems, adverse effects of pesticide use on human health and on the environment in intensive systems and export restrictions due to strict regulations on quarantine pests and limits on pesticide residues. To provide more and better food to populations in both the southern and northern hemispheres in a sustainable manner, there is a need for a drastic reduction in pesticide use while keeping crop pest and disease damage under control. This can be achieved by breaking with industrial agriculture and using an agro- ecological approach, whose main pillar is the conserva- tion or introduction of plant diversity in agroecosystems. Earlier literature suggest that increasing vegetational biodiversity in agroecosystems can reduce the impact of pests and diseases by the following mechanisms: (1) resource dilution and stimulo-deterrent diversion, (2)

https://link.springer.com/content/pdf/10.1007%2Fs13593-011-0022-4.pdf

Plant species diversity for sustainable management of crop pests and diseases in agroecosystems: a review

Methyl bromide is an effective pre-plant soil fumigant used to control nematodes in many high-input, high-value crops in the United States, including vegetables, nursery plants, ornamentals, tree fruits, strawber- ries, and grapes. Because methyl bromide has provided a reliable return on investment for nematode control, many of these commodities have standardized their production practices based on the use of this chem- ical and will be negatively impacted if effective and economical alter- natives are not identified. Alternative control measures based on other chemicals, genetic resistance, and cultural practices require a greater knowledge of nematode biology to achieve satisfactory results. Here, we provide an overview of nematode management practices that we believe will be relied upon heavily in U.S. high-value crop production systems in a world without methyl bromide. Included are case studies of U.S. high-value crop production systems to demonstrate how nematode management practices other than methyl bromide may be incorporated.

Managing nematodes without methyl bromide.

Botrytis cinerea was isolated from infected plants in six greenhouses in Connecticut. Forty-five isolates were evaluated in vitro to determine fungicide sensitivity to benzimidazole (benomyl and thiophanate-methyl) and dicarboximide fungicides (vinclozolin and iprodione). B. cinerea isolates with fungicide resistance were recovered from each greenhouse sampled. Benzimida-zole resistance was more common than dicarboximide resistance (74 to 76% versus 36 to 43%, respectively). Multiple fungicide resistance was common. Nineteen isolates were resistant to both a benzimidazole and a dicarboximide fungicide. The level (EC50) of resistance to dicer-boximides was low compared with resistance to benzimidazoles. Isolate growth rate was not correlated to fungicide sensitivity or EC50. Fungicide resistance was apparently unrelated to the patterns of fungicide use in greenhouses sampled.

/pdf/sensitivity-of-botrytis-cinerea-from-connecticut-greenhouses-356lduwlci.pdf

Sensitivity of Botrytis cinerea from Connecticut Greenhouses to Benzimidazole and Dicarboximide Fungicides

Single potato plants (Solanum tuberosum) cv. Superior were grown in field microplots to evaluate the effects of spent mushroom compost or straw mulch on early dying of potato caused by Verticillium dahliae and/or Pratylenchus penetrans. Prior to planting, soil was fumigated, placed in field microplots, and then infested with pathogens. Area under the senescence progress curve (AUSPC) was greater for plots infested with V. dahliae and/or P. penetrans than for noninfested plots. Plants grown in soil infested with both pathogens developed symptoms earlier than plants grown in soil infested with a single pathogen. Both V. dahliae and P. penetrans reduced yields; the combination of pathogens reduced marketable tuber yields by 22 to 44% (A- and B-sized tubers). Although the total number of tubers of all sizes was not affected by cultural or pathogen treatments, the addition of compost increased marketable tuber weight and decreased AUSPC. Soil amendment with spent mushroom compost may be a means of red...

https://apsjournals.apsnet.org/doi/pdfplus/10.1094/PDIS.1999.83.4.361

Effect of compost amendment or straw mulch on potato early dying disease.

Integrated management of strawberry pests by rotation and intercropping

In September and October 2011, a new disease was observed on Buxus spp. in North Carolina and Connecticut, respectively. In North Carolina, over 10,000 containerized Buxus sempervirens (American boxwood) were affected at one location. A few weeks later, the disease was found in Connecticut on entire plantings of B. sempervirens ‘Suffruticosa’ (English boxwood) at two residential properties, and shortly thereafter on over 150,000 plants at two production nurseries. Initial foliar symptoms appeared as light to dark brown spots, often with dark borders. Spots enlarged and coalesced, often with a concentric pattern, and black streaks or cankers developed on stems. Infected leaves became brown or straw colored and dropped quickly after foliar symptoms were visible. Branch dieback and plant death were also observed in Connecticut. Cultures were isolated from symptomatic leaves and stems and identified as Cylindrocladium pseudonaviculatum Crous, Groenewald & Hill 2002 (1) (syn. Cylindrocladium buxicola Henricot ...

James A. LaMondia

Papers

Managing nematodes without methyl bromide.

Sensitivity of Botrytis cinerea from Connecticut Greenhouses to Benzimidazole and Dicarboximide Fungicides

Effect of compost amendment or straw mulch on potato early dying disease.

Integrated management of strawberry pests by rotation and intercropping

First Report of Boxwood Blight Caused by Cylindrocladium pseudonaviculatum in the United States.