2008International Journal of Plant SciencesRequires access

Untitled research work

Author information unavailable

Open publisher page 0 citations

Abstract

The tapetum, a nutritive tissue necessary for microspore development, is of two basic types in angiosperms: secretory and plasmodial. A third type, invasive nonsyncytial, is possibly intermediate. Secretory tapeta are plesiomorphic in angiosperms, and plasmodial and invasive tapeta are derived types that have evolved several times in early‐divergent angiosperms and particularly in monocots. Many eudicots have secretory tapeta. In this article, records based on new observations for plasmodial and invasive tapeta in eudicots are presented, together with a literature survey. The data indicate that these tapetal types have evolved independently several times in eudicots, particularly in later‐branching lineages. They are rare in early‐divergent eudicots, where they occur only in Berberis and Mahonia (Berberidaceae: Ranunculales). They are recorded in some Amaranthaceae s.l. (Caryophyllales) and in some rosids. Plasmodial and invasive tapeta are more frequent in asterids, where they occur in several families, together with the secretory type. Plasmodial tapeta predominate in Asteraceae (Asterales) and Caprifoliaceae s.l. (Dipsacales). In eudicots, tapetum type is often variable within families or even genera, unlike in early‐divergent angiosperms and especially monocots, where a single tapetum type usually characterizes families or orders. In eudicots, the plasmodium usually forms after the microspores are released from the tetrads, unlike in monocots, where it forms earlier, surrounding the tetrads.

About this research paper

What this paper is about

The tapetum, a nutritive tissue necessary for microspore development, is of two basic types in angiosperms: secretory and plasmodial. A third type, invasive nonsyncytial, is possibly intermediate. Secretory tapeta are plesiomorphic in angiosperms, and plasmodial and invasive tapeta are derived types that have evolved several times in early‐divergent angiosperms and particularly in monocots. Many eudicots have secretory tapeta. In this article, records based on new observations for plasmodial and invasive tapeta in eudicots are presented, together with a literature survey. The data indicate that these tapetal types have evolved independently several times in eudicots, particularly in later‐branching lineages. They are rare in early‐divergent eudicots, where they occur only in Berberis and Mahonia (Berberidaceae: Ranunculales). They are recorded in some Amaranthaceae s.l. (Caryophyllales) and in some rosids. Plasmodial and invasive tapeta are more frequent in asterids, where they occur in several families, together with the secretory type. Plasmodial tapeta predominate in Asteraceae (Asterales) and Caprifoliaceae s.l. (Dipsacales). In eudicots, tapetum type is often variable within families or even genera, unlike in early‐divergent angiosperms and especially monocots, where a single tapetum type usually characterizes families or orders. In eudicots, the plasmodium usually forms after the microspores are released from the tetrads, unlike in monocots, where it forms earlier, surrounding the tetrads.

Why it matters

A significance statement is not available in the OpenAlex record.

Key contribution

A contribution statement is not available in the OpenAlex record.

Method / approach

Method details are not available in the OpenAlex metadata.

Main findings

Findings are not separately available in the OpenAlex metadata.

Limitations

Limitations are not available in the OpenAlex metadata.

Applications

Application details are not available in the OpenAlex metadata.

Available abstract

The tapetum, a nutritive tissue necessary for microspore development, is of two basic types in angiosperms: secretory and plasmodial. A third type, invasive nonsyncytial, is possibly intermediate. Secretory tapeta are plesiomorphic in angiosperms, and plasmodial and invasive tapeta are derived types that have evolved several times in early‐divergent angiosperms and particularly in monocots. Many eudicots have secretory tapeta. In this article, records based on new observations for plasmodial and invasive tapeta in eudicots are presented, together with a literature survey. The data indicate that these tapetal types have evolved independently several times in eudicots, particularly in later‐branching lineages. They are rare in early‐divergent eudicots, where they occur only in Berberis and Mahonia (Berberidaceae: Ranunculales). They are recorded in some Amaranthaceae s.l. (Caryophyllales) and in some rosids. Plasmodial and invasive tapeta are more frequent in asterids, where they occur in several families, together with the secretory type. Plasmodial tapeta predominate in Asteraceae (Asterales) and Caprifoliaceae s.l. (Dipsacales). In eudicots, tapetum type is often variable within families or even genera, unlike in early‐divergent angiosperms and especially monocots, where a single tapetum type usually characterizes families or orders. In eudicots, the plasmodium usually forms after the microspores are released from the tetrads, unlike in monocots, where it forms earlier, surrounding the tetrads.

Key concepts: Eudicots, Tapetum, Biology, Berberidaceae, Botany, Microspore, Typification, Evolutionary biology

Related papers

Back to paper searchBrowse research topicsOriginal source
Untitled research work — Research Paper | ScholarLens