A new method to measure leaf age: Leaf measuring-interval index

We propose a new method, the leaf measuring-interval index (LMI), to estimate leaf age in morphological and physiological studies of leaves. When the plastochron, the interval between the initiation of successive leaves, is constant, the well-known leaf plastochron index (LPI) provides a robust measure of leaf age. When the duration of the plastochron is not uniform, however, we show that the LPI can (in simulations) and does (with actual data) turn variation in duration of the plastochron into variance about the regression estimates of leaf growth curves. The method we present in this paper, the LMI, is plastochron independent. This new method is particularly suited, therefore, for studies of plants growing in natural environments rather than in controlled growth facilities where the assumptions of the LPI method can be met.     

SPECIAL PAPER: THE PLASTOCHRON INDEX: A REVIEW AFTER TWO DECADES OF USE

The plastochron index provides a morphological time scale which has proved more reliable than chronological age in studies relating morphological and physiological development of a whole plant or plant organ. Since its inception in 1957, the index has been utilized in a variety of investigations from leaf ontogeny in cottonwood trees to rhizoid cluster initiation in algae. The plastochron index has been extensively used in studies involving source and sink relationships, leaf anatomy, cell differentiation, and primary vascularization. It has been used in investigations of hormonal regulation of plant growth and in studies of the effects of various environmental factors on developmental processes in crops. This paper reviews some of the literature from 1957 to present concerning the development and use of the plastochron index.     

COMPARISON OF EARLY LATERAL VEIN FORMATION IN LINUM USITATISSIMUM LEAVES WITH THEORETICAL NETWORK MODELS

The plastochron age of the Linum leaf that first exhibited lateral leaf vein divergences, the divergent leaf, increased through shoot ontogeny, but the size of the divergent leaf remained constant. There were progressive decreases in the plastochron and relative plastochron rate of leaf elongation, but no significant change in relative chronological rate of leaf elongation, through ontogeny. Thus, divergent leaves of similar sizes occupied different relative positions in the array of leaves on stems of different plastochron ages. These observations are partially consistent with theoretical network model predictions on early leaf vein development. The empirical data of this study suggest additional features of leaf development that should be incorporated into future simulation models for leaf vein development.     

Assumptions of Plastochron Index: Evaluation With Soya Bean Under Field Drought Conditions

Erickson and Michelini (1957) derived the plastochron index(PI) and a term sometimes referred to as the plastochron ratio(PR), as quantitative expressions of the vegetative developmentof plants. With the stable plant growth in environmental chambersand glasshouses, the assumptions used to derive these termshave been validated. However, more recently these expressionsare being used to characterize growth under the unstable conditionsresulting from the imposition of stress. This study examinesthe validity of the assumptions used to derive PI and PR forfield-grown soya beans [Glycine max (L.) Merrill] subjectedto drought stress. Under stress conditions, the assumptionswere not satisfied. In fact, observing change in PR appearedto be a good method for detecting drought stress in these plants.An alternate method for calculating PI based on a single, youngleaf was developed. This alternate method appeared to be a moresensitive indicator of changes in leaf emergence rate underunstable conditions. Plastochron index, plastochron ratio, Glycine max (L.), soya bean, drought, leaf growth     

LEAF AND APICAL GROWTH CHARACTERISTICS IN TRITICUM

Leaf initiation rate, leaf primordium growth rates, and apical volume growth rates were determined for seedlings of Triticum aestivum cv. Ramona 50 under controlled environmental conditions. Three leaf primordia are present in the caryopsis, and three more leaves are initiated within the first two weeks after germination with a mean plastochron length of 95.5 hr. Volume growth rates of the apical region were determined on six apices which had six primordia each. The mean radial expansion rate was 0.467/plastochron, and the vertical expansion rate was 0.457/plastochron. The volume expansion rate was 1.393/plastochron. The mean volume doubling time was 0.498 plastochrons or 47.1 hr.     

The determination of pea leaves,leaflets, and tendrils

Pea leaf determination was examined by culturing excised leaf, leaflet, and tendril primordia of different ages on a nutrient medium. Pinna primordia were designated as 1) determined, if they grew normally in culture; 2) undetermined, if they grew into differentiated structures that were morphologically and anatomically different from either leaflet or tendril; or 3) partially determined, if the two pinnae of an opposite pair developed unequally in isolation, or for leaflet pinnae only, if laminae were initiated but did not develop completely. The compound pea leaf as a whole is determined over four plastochrons of development. Proximal pinnae are determined during the second leaf plastochron, approximately 0.8 plastochron after their initiation. The second most proximal pair of pinnae is determined during the third plastochron, and the terminal portion of the rachis is determined last, during the fourth plastochron. Determination of leaflet dorsiventrality is gradual, requiring a critical minimum period with the leaf in physiological contact with the shoot system. The rachis primordium, when isolated from the shoot, does not affect determination of its pinnae as leaflets or tendrils. Afila and tendril-less homeotic mutations do not alter the timing of pinna determination.     

Rates of corolla growth in tobacco determined with the plastochron index

The growth of vegetative and reproductive shoots of Nicotiana tabacum L. cv. Xanthi is analyzed with the plastochron index to estimate the relationship between corolla growth and time. The plastochron of leaves 9 through 20 declines steadily at each successive node. The flower plastochron increases steadily during the growth of an individual cyme, with the most distal flower to open having the longest plastochron. Variation in the flower plastochron is the result of variation in the rate of flower initiation, not the growth rate of individual flowers. The corolla has an extended phase of approximately constant relative growth in length (between 0.2 · d^–1 and 0.3 · d^–1) until a peak of growth (0.5 · d^–1) 2–3 d before anthesis. Corollas also have periodic peaks and troughs of growth that are low in amplitude (0.1 · d^–1), but persist throughout most of corolla development. The pattern of corolla expansion contrasts strongly with earlier reports of the pattern of tobacco leaf growth.Abbreviations PI plastochron index - PR plastochron ratio - RGR relative growth rate in length The authors thank: Drs. T. Sage and E.G. Williams for the considerable time and space they invested; the members of Dr. R. Wyatt's laboratory for allowing us to use their computer facilities; A. Tull and M. Smith for their care taken in the green-house. This research was supported by U.S. Department of Agriculture grant GAM-89-01056 and by National Science Foundation grant DCB-87-15799.     

PLASTOCHRON INDICES FOR JUVENILE AND MATURE FORMS OF HEDERA HELIX L. (ARALIACEAE)

English ivy (Hedera helix) plants were assessed for the applicability of the plastochron index (PI). Juvenile ivy satisfied all requirements for the use of the PI and showed a plastochron of 4.23 days. Mature ivy grown under long day conditions flowered after 11–12 leaves. Two distinct groups of leaves were produced with different plastochrons (0.83 and 3.2 days, respectively) and leaf morphologies. Long-day-grown ivy did not satisfy the requirements for the use of the PI. Short-day-grown mature ivy continued production of leaves beyond the 12th leaf. Vegetative growth was perpetuated for at least 25 plastochrons. By 19 plastochrons (ca. 41 days after budbreak) a linear PI vs. time relationship was established with a plastochron of 3.16 days. This newly acquired ability to maintain vegetative growth in mature ivy plants may allow a direct comparison with the vegetative indeterminant juvenile in order to assess possible anatomical factors responsible for phase stability and phase change using the PI as a basis for comparison.     

COMPARATIVE FLOWER DEVELOPMENT IN THE CLEISTOGAMOUS SPECIES VIOLA ODORATA. I. A GROWTH RATE STUDY

In Viola odorata, chasmogamous (CH) or open flowers and small, short-petioled leaves are produced under 11 hr or less of daylight, cleistogamous (CL) or closed flowers and large, long-petioled leaves under 14 hr or more of daylight, and intermediate floral and leaf forms under transitional photoperiods. CL flowers are approximately four times smaller than CH flowers and differ morphologically in repressed growth of the anterior petal spur and staminal nectaries, and recurving of the style which remains enclosed within the cone formed by anther appendages. Both CH and CL shoot systems conform to a (2 + 3) phyllotaxis with minor differences in leaf divergence angles and phyllotactic indices. The larger CL leaf grows significantly faster than the CH leaf, and an increased rate of leaf initiation occurs in the CL apex represented by a plastochron of 3.4 days compared to 4.3 days in the CH apex. The plastochron index was used to indirectly age young floral primordia nondestructively until prophase of meiosis I within the anthers. This event occurs 8 days earlier in the CL than the CH flower. Time from meiosis until flower maturity, determined by direct observation, is about 14 days for the CL flower, versus 21 days for the CH flower.     

A METHOD FOR DETERMINING PLASTOCHRON INDICES DURING HETEROBLASTIC SHOOT GROWTH

A plastochron is defined as the time interval between two successive recurring events during the growth of plant shoots, such as leaf initiation. The plastochron index (PI) formulated by Erickson and Michelini (1957, American Journal of Botany 44: 297–305) provides a method for determining 1) morphological equivalence in a developmentally variable sample of shoots and 2) rates of development in microscopic tissues and organs, by expressing shoot age as a function of plastochron number. The PI assumes that homologous organs at successive nodes grow exponentially, at equal rates, and the plastochron remains constant. These three conditions are not met in many shoots that exhibit heteroblasty in their plastochron and the growth rate of organs at successive nodes. An alternative computational method for the PI is presented that uses two measurements taken at different times from the same organ during its exponential growth phase. The method does not assume that the PI is a linear function of time. Results of an analysis of cyme internode growth in two races of Arenaria uniflora (Caryophyllaceae) demonstrate that the method proposed is in good agreement with Erickson and Michelini's (1957) method when shoot growth is not markedly heteroblastic. The current method is also used to determine the nonlinear relation between PI and time in a race of A. uniflora that has heteroblastic cyme growth. The results generalize the PI for use in studies of heteroblasty, and for shoots where the relative plastochron rate cannot be directly determined.     

CHANGES IN EPILOBIUM PHYLLOTAXY INDUCED BY N-1-NAPHTHYLPHTHALAMIC ACID AND α-4-CHLOROPHENOXYISOBUTYRIC ACID

Preliminary studies establishing relationships between leaf plastochron index and Epilobium hirsutum L. shoot growth provide a method for rigorous selection of plants utilized in experiments designed to test the working hypothesis that endogenous auxin gradient interactions are factors of phyllotactic control in this species. Application of N-1-naphthylphthalamic acid (NPA), an auxin transport inhibitor, to one of the youngest bijugate primordia on the shoot meristem results in increased growth of the treated primordium. Fasciation between the treated primordium and one of the next primordia to be initiated alters relative vertical spacing of primordia. Angular shifts between subsequent primordia result in spiral transformation of Epilobium bijugate phyllotaxy. Application of α-4-chlorophenoxyisobutyric acid (CPIB), an auxin antagonist, to one of the youngest bijugate primordia on the shoot meristem results in decreased growth of the treated primordium that alters both radial and vertical spacing of primordia. This is followed by angular shifts between subsequent primordia resulting in spiral transformation of the bijugate phyllotaxy. Changes in the growth parameters of NPA- and CPIB-treated shoots are similar. Relative plastochron rates of radial and vertical shoot growth of induced spiral shoots are about half those of lanolin paste control shoots, as are the plastochrons and relative plastochron rates of leaf elongation. Treated shoot meristems have eccentricities of 0.5 as compared to bijugate control meristem eccentricities of 0.7. No significant difference is apparent between basal transverse areas of treated and control shoot meristems. The relative chronological rates of growth of treated shoots are not significantly different from those rates of control shoots. Spiral transformation results from changes in relative positions of leaf primordia insertion on the shoot meristem, not from changes in growth of treated shoots. These changes are accompanied by an increased rate of leaf initiation on a more circular shoot meristem. Existing theoretical models of phyllotaxy are discussed in relation to these chemically induced changes of Epilobium leaf arrangement.     

Dual effects of miR156-targeted SPL genes and CYP78A5/KLUH on plastochron length and organ size in Arabidopsis thaliana

Leaves of flowering plants are produced from the shoot apical meristem at regular intervals, with the time that elapses between the formation of two successive leaf primordia defining the plastochron. We have identified two genetic axes affecting plastochron length in Arabidopsis thaliana. One involves microRNA156 (miR156), which targets a series of SQUAMOSA PROMOTER BINDING PROTEIN-LIKE (SPL) genes. In situ hybridization studies and misexpression experiments demonstrate that miR156 is a quantitative, rather than spatial, modulator of SPL expression in leaf primordia and that SPL activity nonautonomously inhibits initiation of new leaves at the shoot apical meristem. The second axis is exemplified by a redundantly acting pair of cytochrome P450 genes, CYP78A5/KLUH and CYP78A7, which are likely orthologs of PLASTOCHRON1 of rice (Oryza sativa). Inactivation of CYP78A5, which is expressed at the periphery of the shoot apical meristem, accelerates the leaf initiation rate, whereas cyp78a5 cyp78a7 double mutants often die as embryos with supernumerary cotyledon primordia. The effects of both miR156-targeted SPL genes and CYP78A5 on organ size are correlated with changes in plastochron length, suggesting a potential compensatory mechanism that links the rate at which leaves are produced to final leaf size.     

Transgenic tobacco over-expressing a homeobox gene shows a developmental interaction between leaf morphogenesis and phyllotaxy.

The tobacco gene, NTH1, encodes a polypeptide of 326 amino acids and is a member of the class1 KN1-type family of homeobox genes. Expression of NTH1 has mainly been observed in vegetative and reproductive shoot apices, not observed in roots or expanded leaves. Over-expression of NTH1 in transgenic plants caused abnormal leaf morphology, consisting of wrinkling and curvature. Interestingly, the direction of leaf curvature tended to be conserved among almost all of the leaves in any given transformant. In transgenic plants exhibiting clockwise or anticlockwise phyllotaxy, leaves curved to the right or left, respectively, when looking from the shoot apex toward the base. Micro-surgical experiments demonstrated that the presence of the shoot apex is necessary for the development of leaf curvature, indicating that the order of formation of leaves on the stem (the generative spiral) affects leaf development. We found a correlation between the severity of leaf curvature and the value of the plastochron ratio, a parameter of phyllotaxy. Transformants with more severe phenotypes had larger plastochron ratios. From these findings, we discuss the possibility that an increase in the plastochron ratio, caused by over-expression of NTH1 in the shoot apex, may be involved in leaf curvature.     

PLASTOCHRON2 regulates leaf initiation and maturation in rice

In higher plants, leaves initiate in constant spatial and temporal patterns. Although the pattern of leaf initiation is a key element of plant shoot architecture, little is known about how the time interval between initiation events, termed plastochron, is regulated. Here, we present a detailed analysis of plastochron2 (pla2), a rice (Oryza sativa) mutant that exhibits shortened plastochron and precocious maturation of leaves during the vegetative phase and ectopic shoot formation during the reproductive phase. The corresponding PLA2 gene is revealed to be an orthologue of terminal ear1, a maize (Zea mays) gene that encodes a MEI2-like RNA binding protein. PLA2 is expressed predominantly in young leaf primordia. We show that PLA2 normally acts to retard the rate of leaf maturation but does so independently of PLA1, which encodes a member of the P450 family. Based on these analyses, we propose a model in which plastochron is determined by signals from immature leaves that act non-cell-autonomously in the shoot apical meristem to inhibit the initiation of new leaves.     

NOMOGRAM FOR THE PLASTOCHRON INDEX

Erickson , Ralph O. (U. Pennsylvania, Philadelphia.) Nomogram for the plastochron index. Amer. Jour. Bot. 47(5) : 350—351. Illus. 1960.–In an earlier paper, a plastochron index was described which specifies the development age of a shoot with some precision. The plastochron index of a shoot can be estimated quickly by use of the nomogram described here.     

Comparison of Leaf Plastochron Index and Allometric Analyses of Tooth Development in Arabidopsis thaliana

Abstract Two methods of analyses were used to investigate tooth development in serrate (se) mutant and wild-type Columbia-1 (Col-1) Arabidopsis thaliana leaves. There were almost twice as many teeth with deeper sinuses and two orders of toothing on the margins of serrate compared with Columbia-1 leaves. The main objective of this study was to test three hypotheses relative to the source of polymorphism in tooth development: (i) Teeth share similar growth rates and initial sizes, but the deeper teeth are initiated earlier in leaf development. (ii) Teeth share similar timing of initiation and growth rates, but the deeper teeth have a larger initial size. (iii) Teeth share similar timing of initiation and initial sizes, but the deeper teeth have a faster growth rate. Leaf plastochron index (LPI) was used as the time variable for leaf development. Results showed teeth in se were initiated at −27 LPI, 15 plastochrons earlier than those of Col-1. Serrate leaf expansion was biphasic, with the early phase expanding at half the relative plastochron rate of the later phase, which equaled the constant relative expansion rate of Col-1 leaves. Allometric analyses of tooth development obscured the interactions between time of tooth and leaf initiation and the early phase of leaf expansion characteristic of serrate leaves and teeth. Timing of developmental events that allometric analysis obscured can be readily detected with the LPI as a developmental index. Received 25 January 2000; accepted 17 March 2000     

ROLE OF STEM GROWTH IN LINUM USITATISSIMUM LEAF TRACE PATTERNS

Linum usitatissimum stem growth parameters were quantified by computer-assisted analyses of scanning electron micrographs of shoot apical meristems throughout ontogeny. There were progressive decreases in the plastochron and relative plastochron rates of radial and vertical stem growth which resulted in the generation of progressively higher orders of contact parastichy phyllotaxis throughout ontogeny. The change in the relative spacing of primordia initiation on the stem coupled with the iterative differentiation of leaf gap and interfascicular ray parenchyma associated with each leaf primordium resulted in the delimitation of progressively higher orders of leaf trace interconnections throughout ontogeny. A set of developmental rules was generated which should permit simulation of many leaf trace patterns.     

Growth changes in the shoot apex of Sinapis alba during transition to flowering

The aim of the work was to report morphological changes whichoccur in the shoot apex during the morphogenetic switch to floweringin the model long day (LD) plant, Sinapis alba. During the floraltransition induced by 1 LD the growth rate of all componentsof the shoot apex is modified profoundly. The earliest changes,detected at 24 h after start of LD, include a decrease in plastochronduration and an increase of growth of leaf primordia. One daylater, the meristem dome starts to increase in volume, apicalinternodes have an increased height and there is a precociousoutgrowth of axillary meristems. All these changes precede initiationof flower primordia, which starts at about 60 h after the startof LD. Later changes include meristem doming, a decrease inthe plastochron ratio and a shift to a more complex phyllotaxis.All the changes, except the decreased plastochron ratio, arecharacteristics of an apex with an increased tempo of growth.The stimulation of longitudinal growth (height of apical intemodes)is more marked and occurs earlier than the reduction of radialgrowth (plastochron ratio). Key words: Axillary meristem, internode growth, leaf growth, plastochron ratio, plastochron duration     

FLORAL INDUCTION DOES NOT ALTER THE GROWTH PARAMETERS OF FUCHSIA

Floral induction by night interruption of Fuchsia hybrida cv. Lord Byron, a quantitative long-day plant with decussate phyllotaxis and an indeterminate flowering habit, altered neither the rate of leaf initiation nor the rate of leaf expansion; nor did flower initiation and development change the vegetative growth of the plants. This was diagnosed using plastochron duration and plastochron ratio measurements before, during, and after a 10-day induction period. A comparison between indeterminate and determinate flowering is made using these two parameters.