Japanese holly

The disease develops in overly wet, poorly aerated substrate and attacks the roots and the base of the stem. The roots turn brown, rot and lose their bark, which slips off easily, and a dark, watery rot appears at the stem base. The above-ground part wilts, yellows and dies back despite moist soil – a characteristic symptom, because the damaged roots no longer take up water. Especially at risk are houseplants, succulents and cacti (from overwatering), and in the ground conifers, rhododendrons, ericaceous plants and strawberries on waterlogged sites. The process begins inconspicuously at the root hairs and root tips, which darken and disappear, after which the rot advances towards the framework roots and the root collar. Healthy, pale, active roots waste away — what remains is a dark, rusty-brown or blackish, watery mass, and the outer layer of the root bark slips off like a glove, exposing the discoloured central cylinder. In trees and shrubs, infection of the collar and the base of the trunk (stem-base rot) shows as a dark, often streaking patch, sometimes with oozing, and the bark there is moist and sunken; in conifers and rhododendrons, browning and dieback are seen from the bottom or from the centre of the crown while the soil is still moist. Characteristic is the nested (patchy) occurrence of symptoms in the bed — where water and the pathogen accumulate locally. It is worth distinguishing the two causal oomycete genera: Pythium mainly attacks seedlings and fine roots, causing damping-off and root rot in cool, wet substrate, whereas Phytophthora also attacks older, woody plants, framework roots and the collar, more strongly in warmer, water-saturated soil. Key for diagnosis is the contradiction of the symptoms: the plant wilts and looks 'dry', although the substrate is wet — this results from the destruction of the roots, not from a shortage of water.

The symptom affects acid-loving plants — hydrangea, rose, rhododendron, blueberry and others — grown on alkaline or calcareous soils. The leaf blade turns yellow while the veins remain distinctly green, producing the characteristic interveinal chlorosis. The symptoms appear first on the youngest leaves at the shoot tips, because iron is not very mobile within the plant and is not translocated into new growth. In extreme cases the leaves are almost white and their margins dry out. Crucially, the cause is usually not a lack of iron in the soil but too high a pH, which blocks its uptake by the roots. It is worth noting that not all susceptible plants are equally acid-loving — the rose prefers a slightly acidic to neutral reaction (about pH 6–7) and also develops iron chlorosis on strongly alkaline, calcareous soils, although it is not acid-loving in the way rhododendron or blueberry is. The pattern of yellowing is very regular: not only the main vein stays green but the whole fine network of veins, so that the leaf looks like green lace on a yellow-green background — this is the most reliable diagnostic feature, distinguishing interveinal chlorosis from the uniform, whole-surface yellowing typical of nitrogen deficiency. The symptoms intensify with each successive flush: older leaves at the base of the shoot may still be green or only slightly paled, and the younger the leaf, the paler it is, up to almost white, lemon-yellow tips. Under a long-lasting deficiency the margins and tips of the youngest leaves turn brown and necrotic, shoots grow more weakly and become smaller, and in blueberry the yield and fruit quality decline. Iron chlorosis is not contagious — it does not spread from plant to plant but appears simultaneously in all specimens growing on the same, overly alkaline site, which also helps to distinguish it from infectious diseases. Its severity can vary through the season: cold, wet and compacted soil, poor root aeration, excess calcium, a high bicarbonate content in the watering water, and over-fertilization with phosphorus additionally hinder iron uptake and aggravate the symptoms even when the element is not lacking in the soil.

On leaves, shoots and fruit a black, soot-like coating forms that can be partly wiped off with a finger. These fungi do not infect the plant tissue – they grow on the sweet, sticky honeydew excreted by aphids, whiteflies, mealybugs, psyllids and scale insects. The coating therefore appears exactly where these pests feed, and its main harm is that it masks the leaf blade, reduces photosynthesis and disfigures the plants. The symptom is often seen on citrus, lime, maple and on houseplants and greenhouse plants. The coating may be thin and cobweb-like or thick, crusty and dull black — depending on the fungus species and the amount of honeydew; on evergreen plants it can persist through the whole winter. A key identifying feature: after the blade is wiped, healthy green tissue emerges from beneath the black layer — sooty mould leaves no spots, necrosis or pitting, because it does not penetrate the leaf. The extent of the symptom is also characteristic: the soot settles where the sticky honeydew drips, so it appears not only on leaves but also on objects beneath the plant — the pavement, garden furniture, a windowsill or car bodywork — which in itself reveals pests feeding higher up. The sooty mould fungi themselves are dark-pigmented (melanised) saprotrophs, which is why the layer is deeply black. Direct damage to the plant is usually moderate — weakening through leaf shading, loss of vigour, poorer appearance and reduced market value of fruit or ornamental plants — but a dense, long-lasting coating on many leaves genuinely limits assimilation and growth. Sooty mould is best treated as a visible signal that a colony of sap-sucking insects is developing higher up on the plant (or on a tree above it).

Immobile, brown or yellowish shields (1-4 mm) attached to stems and the underside of leaves, especially along the veins. Easily mistaken for growths on the plant. They suck sap, causing yellowing and weakening, and excrete sticky honeydew. Common on figs, orchids and plants with tough leaves. The collective name covers two groups with different biology. Armoured scales (Diaspididae) have a hard waxy shield separate from the body, which can be prised off - beneath it emerges a tiny, legless and wingless female; they do not excrete honeydew. Soft scales (Coccidae) have a convex, cup-shaped cover fused with the body, and it is they that excrete it abundantly. Sticky honeydew - the domain of soft scales and other honeydew-producing scale insects, not of armoured scales - settles on the leaves and attracts sooty mould fungi (sooty mould, sooty blotch) as well as ants, which defend the colony against predators. The only mobile feeding stage is the crawler - a flat, tiny larva which, after hatching from beneath the mother's shield, disperses over the plant, then settles, inserts its stylet into the conducting tissues and loses the ability to move; adult females remain immobile for the rest of their lives. Males pupate and, as tiny, winged, short-lived insects, do not feed. In heated interiors the pest breeds all year round, producing several overlapping generations; outdoors usually 1-3 generations, and fertilised females or eggs hidden beneath the shield overwinter. Feeding symptoms are yellowing and premature leaf drop, dieback of shoots, stunting and weakening of the plant, and secondarily a black coating of sooty mould on leaves covered with honeydew. On fruit trees infested by San Jose scale (Comstockaspis perniciosa), reddish discolouration appears around the feeding sites, and heavily colonised branches die back. Because the shields are immobile and their colour blends into the bark and veins, an infestation is easily overlooked until honeydew appears or the plant is noticeably weakened - which is why regular inspection of the leaf undersides and shoot axils is key.

A soft scale whose females form brown, dome-shaped, strongly convex "cups" (3–6 mm) sitting motionless on shoots, twigs and leaf bases. They suck sap, weakening the plants, and excrete abundant honeydew on which black sooty mould develops, disfiguring leaves and fruit. It feeds on fruit trees (plum, peach), grapevine, ornamental shrubs and houseplants. It belongs to the soft scales (Coccidae), not to the true armoured scales — its brown shield is the sclerotized body of the female and cannot be separated from her. In the Polish climate it usually develops one generation per year. It overwinters as an immature larva (second instar) attached to shoots and twigs, in bark crevices and near the buds. In spring the larvae resume feeding and the females grow quickly, turning into the characteristic, hardening "cups". Beneath its shield the mature female lays numerous eggs — often from several hundred to over a thousand. The crawling larvae (so-called crawlers) that hatch from them, usually at the turn of June and July, spread out onto the leaves and young shoots, where they attach and feed; before leaf fall they return to the shoots to overwinter. Symptoms of infestation are weakened growth and dieback of twigs under heavy attack, sticky, glossy honeydew on the leaves and beneath the plant, a black sooty coating that hampers photosynthesis, and numerous ants feeding on the honeydew. The larvae and females cluster in the forks of twigs, on the undersides of shoots, at the base of the leaves and along the veins and leaf stalks.

Tiny (0.3–0.5 mm) arachnids, hard to spot with the naked eye, feeding on the underside of leaves. Symptoms: fine, pale speckling (feeding punctures); over time the leaves turn grey, yellow and dry out. Under heavy infestation a fine webbing becomes visible. Warm, dry air favours their development — a common problem for houseplants in winter near radiators. Spider mites are not insects but mites of the family Tetranychidae — adults have 8 legs (larvae only 6). The most common in cultivation is the two-spotted spider mite (Tetranychus urticae): yellowish-green females carry two dark spots on the sides of the body, while overwintering females turn orange-red. In orchards the fruit tree red spider mite (Panonychus ulmi) is frequent, whose red eggs overwinter in clusters on the bark of the shoots. Feeding mechanism: the mites puncture the cells of the epidermis and mesophyll on the underside of the leaf and suck out their contents, and the emptied cells fill with air — hence the characteristic, silvery-grey, fine speckling visible from the upper side of the blade (resembling a mosaic discolouration). At high numbers the leaves turn brown, curl and drop prematurely, and the whole plant weakens and loses its growth. Dense webbing spun between the leaves and shoot tips appears only under an advanced attack and is a sign of the risk of the pest spreading to neighbouring plants. The development cycle is very fast in warmth and drought — at a temperature of 25–30°C a single generation can be completed in 1–2 weeks, hence the numerous generations per season and the rapid, exponential build-up of the population. Females lay spherical, transparent eggs on the underside of the leaves. Fertilised females overwinter (in bark crevices, leaf litter and plant debris) or — in the fruit tree red spider mite — the eggs on the bark. Early infestation is easy to miss; diagnosis is helped by shaking a leaf over a white sheet of paper (moving specks become visible) or examining the underside of the leaf with a magnifying glass.

Weevils 8-12 mm long, black or dark brown, with a short, broad snout, flightless and active at night. Their larvae are white, legless, C-shaped, with a brown head, and live in the soil. Symptoms: the adult beetles notch characteristic semicircular bites into leaf margins at night (box, rhododendron, bergenia, strawberry, houseplants), while the larvae gnaw at roots, bulbs and the base of shoots, causing the plant to wilt suddenly and die. The most common is the black vine weevil (Otiorhynchus sulcatus), more rarely the strawberry root weevil (O. ovatus) and related species. A key factor behind their numbers is parthenogenetic reproduction (virgin birth): populations consist almost exclusively of females, and a single female lays several hundred eggs into the soil without a male, so an outbreak builds up quickly. Life cycle: the beetles overwinter mainly as larvae (some as adults) in the soil; the adults emerge in late spring and early summer and for about 3-4 weeks carry out maturation feeding on the leaves before they begin to lay eggs, while the larvae feed on roots from summer through autumn and again in early spring. The larval stage is the most dangerous - the larvae chew the roots and gnaw the root collar at the base of the shoot (girdling), causing the plant to wilt suddenly despite moist soil and to lift easily out of the substrate; adult feeding (semicircular notches on leaf margins) mainly disfigures the plant and rarely kills it. Plants in containers are particularly at risk, where the limited root ball is quickly destroyed. The beetles are flightless, so they spread by walking across the substrate and - above all - with infested plants and substrate, which makes newly bought potted plants the main route of introduction.